FM 3-11-9 (Chemical Biological Agents)

Survival, Water, Medical Field Manuals

Military Manuals

Document text

ARMY, MARINE CORPS, NAVY, AIR FORCE 




POTENTIAL MILITARY 

CHEMICAL/BIOLOGICAL 

AGENTS AND 

COMPOUNDS 



FM 3-11.9 

MCRP 3-37.1B 

NTRP 3-11.32 

AFTTP(I) 3-2.55 



JANUARY 2005 



DISTRIBUTION RESTRICTION: 
Approved for public release; 
distribution is unlimited. 



MULTISERVICE TACTICS, TECHNIQUES, AND PROCEDURES 



FOREWORD 

This publication has been prepared under our direction for use by our respective 
commands and other commands as appropriate. 





STANLEY H. LILLIE 

Brigadier General, USA 

Commandant 

US Army Chemical School 



EDWARD HANLON, JR. 

Lieutenant General, USMC 
Deputy Commandant 
for Combat Development 




TC&zttu. — , 




JOHN M. KELLY 

Rear Admiral, USN 

Commander 

Navy Warfare Development Command 



BENTLEY B. RAYBURN 

Major General, USAF 

Commander 

Headquarters Air Force Doctrine Center 



This publication is available at Army 
Knowledge Online <www.us.army.mil> . 



PREFACE 



1. Scope 

This document provides commanders and staffs with general information and 
technical data concerning chemical/biological (CB) agents and other compounds of 
military interest such as toxic industrial chemicals (TIC). It explains the use; 
classification; and physical, chemical, and physiological properties of these agents 
and compounds. Users of this manual are nuclear, biological, and chemical 
(NBC)/chemical, biological, and radiological (CBR) staff officers, NBC 
noncommissioned officers (NCOs), staff weather officers (SWOs), NBC medical 
defense officers, medical readiness officers, medical intelligence officers, field 
medical treatment officers, and others involved in planning battlefield operations in 
an NBC environment. 



2. Purpose 

This publication provides a technical reference for CB agents and related 
compounds. The technical information furnished provides data that can be used to 
support operational assessments based on intelligence preparation of the battlespace 
(IPB). 



3. Application 

The audience for this publication is NBC/CBR staff personnel and 
commanders tasked with planning, preparing for, and conducting military 
operations. 



4. Implementation Plan 

Participating service command offices of primary responsibility (OPRs) will 
review this publication, validate the information, and reference and incorporate it in 
service and command manuals, regulations, and curricula as follows: 

Army. The United States Army (USA) will incorporate this publication in 
USA training and doctrinal publications as directed by the Commander, United 
States Army Training and Doctrine Command (TRADOC). Distribution is in 
accordance with Department of the Army (DA) Form 12-99-R (Initial Distribution 
Requirements for Publications). 

Marine Corps. The United States Marine Corps (USMC) will incorporate 
the procedures in this publication in USMC training and doctrinal publications as 
directed by the Commanding General (CG), United States Marine Corps Combat 



Development Command (MCCDC). Distribution is in accordance with Marine Corps 
Publication Distribution System (MCPDS). 

Navy. The United States Navy (USN) will incorporate these procedures in 
USN training and doctrinal publications as directed by the Commander, Navy 
Warfare Development Command (NWDC). Distribution is according to the military 
standard requisitioning and issue procedures (MILSTRIP). 

Air Force. The United States Air Force (USAF) will validate and 
incorporate appropriate procedures according to applicable governing directives. 



5. User Information 

a. The United States Army Chemical School (USACMLS) developed this 
publication with the joint participation of the approving service commands. 

b. We encourage recommended changes for improving this publication. Please 
reference the specific page and paragraph, and provide a rationale for each 
recommendation. Send comments and recommendations directly to — 



Army 

Commandant 

US Army Chemical School 

ATTN: ATSN-CM-DD 

401 MANSCEN Loop, Suite 1029 

Fort Leonard Wood, MO 65473-8926 

COMM (573) 596-0131, extension 3-7364 



Marine Corps 

Commanding General 

US Marine Corps Combat Development Command 

ATTN: C42 (Director) 

3300 Russell Road 

Quantico, VA 22134-5001 

DSN 278-6234; COMM (703) 784-6234 



Navy 

Commander 

Navy Warfare Development Command 

ATTN: N5 

686 Cushing Road 

Newport, Rl 02841-1207 

DSN 948-4201; COMM (401) 841-4201 



Air Force 

HQ Air Force Doctrine Center 

ATTN: DJ 

155 North Twining Street 

Maxwell AFB, AL 36112-6112 

DSN 493-7224; COMM (334) 953-7224 



*FM 3-11.9 

MCRP 3-37.1B 

NTRP 3-11.32 

AFTTP(I) 3-2.55 



FM 3-11.9 US Army Training and Doctrine Command 

Fort Monroe, Virginia 

MCRP 3-37. IB Marine Corps Combat Development Command 

Quantico, Virginia 

NTRP 3-11.32 Naval Warfare Development Command 

Newport, Rhode Island 

AFTTP(I) 3-2.55 Headquarters Air Force Doctrine Center 

Maxwell Air Force Base, Alabama 

10 January 2005 



POTENTIAL MILITARY CHEMICAL/BIOLOGICAL AGENTS AND 

COMPOUNDS 

TABLE OF CONTENTS 

Page 

EXECUTIVE SUMMARY xiii 

CHAPTER I INTRODUCTION 

Background l-l 

Threat I-2 

Militarily Significant Aspects of Toxic Chemical Agents I-4 

Militarily Significant Aspects of Biological Agents I-7 

Militarily Significant Aspects of Toxic Industrial Chemicals l-ll 

CHAPTER II CHEMICAL WARFARE AGENTS AND THEIR PROPERTIES 

Background Il-l 

Definitions of Selected Physical and Chemical Properties Il-l 

Definitions of Toxicity-Related Terms II-4 



DISTRIBUTION RESTRICTION: Approved for public release; distribution is unlimited. 
*This publication supersedes FM 3-9, 12 December 1990. 



IV 



CHAPTER III 



CHAPTER IV 



CHAPTER V 



APPENDIX A 
APPENDIX B 
APPENDIX C 
APPENDIX D 

APPENDIX E 

APPENDIX F 

APPENDIX G 

APPENDIX H 



Choking Agents 11-9 

Nerve Agents 11-13 

Blood Agents 11-31 

Blister Agents (Vesicants) 11-37 

Incapacitating Agents 11-64 

Chemical Warfare Agent Precursors 11-68 

Other Chemical Warfare Agents 11-76 

MILITARY CHEMICAL COMPOUNDS AND THEIR PROPERTIES 

Background Ill-l 

Riot Control Agents (Tear- Producing Compounds) Ill-l 

Respiratory Irritants 111-7 

Obsolete Riot Control Agents 111-14 

Smokes, Obscurants, and Incendiaries 111-16 

BIOLOGICAL AGENTS AND THEIR PROPERTIES 

Background IV-1 

Bacterial Agents of Potential Concern IV-4 

Rickettsiae of Potential Concern IV-11 

Viral Agents of Potential Concern IV- 14 

Toxins of Potential Concern IV-22 

TOXIC INDUSTRIAL CHEMICALS AND THEIR PROPERTIES 

Background V-l 

Other Information Sources V-2 

Reach-Back Capability V-4 

TABLE OF EQUIVALENTS A-l 

TEMPERATURE CONVERSIONS B-l 

PERIODIC TABLE OF THE ELEMENTS C-l 

CHEMICAL WEAPONS CONVENTION SCHEDULE 1, 2, 

AND 3 CHEMICALS D-l 

CHEMICAL WARFARE AGENT PRECURSOR CHEMICALS: 

USES AND EQUIVALENTS E-l 

CHEMICAL WARFARE AGENTS AND OTHER MILITARY 

CHEMICAL COMPOUNDS F-l 

PROPERTIES OF CHEMICAL WARFARE AGENTS AND MILITARY 
CHEMICAL COMPOUNDS G-l 

TOXICITY PROFILE ESTIMATES H-l 



Background H-l 

Choking Agents H-l 

Nerve Agents H-l 

Blood Agents H-16 

Blister Agents H-17 

Respiratory Irritants H-32 

APPENDIX I PROPERTIES OF SELECTED BIOLOGICAL AGENTS 1-1 

APPENDIX J SELECTED ANIMAL PATHOGENS J-l 

Background J-l 

Animal Diseases J-l 

APPENDIX K SELECTED PLANT PATHOGENS K-l 

Background K-l 

Bacterial Diseases K-l 

Fungal Diseases K-2 

Viral Diseases K-5 

APPENDIX L DISSEMINATION OF BIOLOGICAL AGENTS L-l 

Background L-l 

Inhalation or Aerosol Route of Entry L-l 

Percutaneous Route of Entry L-3 

Oral Route of Entry L-4 

Covert Dissemination L-4 

REFERENCES References-1 

GLOSSARY Glossary-1 

INDEX Index-l 

FIGURES ll-l The TLE Effect on the Ct Profile 11-7 

11-2 Ct Profile for Dosage versus Exposure Duration 11-8 

G-l Vapor Pressure of Choking Agents G-19 

G-2 Vapor Pressure of Nerve Agents G-20 

G-3 Vapor Pressure of Blood Agents G-21 

G-4 Vapor Pressure of Blister Agents G-22 

G-5 Vapor Pressure of Incapacitating Agents (BZ) G-23 

G-6 Vapor Pressure of Riot Control Agents (Capsaicin) G-24 

G-7 Vapor Pressure of Respiratory Irritants G-25 

H-l GA Vapor: Dosage versus Exposure Duration H-3 



VI 



H-2 GA Vapor: Concentration versus Exposure 

Duration H-4 

H-3 GB Vapor: Dosage versus Exposure Duration H-6 

H-4 GB Vapor: Concentration versus Exposure 

Duration H-7 

H-5 GD Vapor: Dosage versus Exposure Duration H-9 

H-6 GD Vapor: Concentration versus Exposure 

Duration H-10 

H-7 GF Vapor: Dosage versus Exposure Duration H-12 

H-8 GF Vapor: Concentration versus Exposure 

Duration H-13 

H-9 VX Vapor: Dosage versus Exposure Duration H-15 

H-10 VX Vapor: Concentration versus Exposure 

Duration H-16 

H-ll HD Vapor: Dosage versus Exposure Duration H-19 

H-12 HD Vapor: Concentration Versus Exposure 

Duration H-19 

TABLES ll-l List of Selected CW Agents and Precursors 1-1 

11-2 CG 11-10 

11-3 CG Toxicity Estimates 11-11 

11-4 DP 11-12 

11-5 DP Toxicity Estimates 11-13 

11-6 GA 11-14 

11-7 GA Toxicity Estimates 11-17 

11-8 GB 11-18 

11-9 GB Toxicity Estimates 11-20 

11-10 GD 11-21 

11-11 GD Toxicity Estimates 11-23 

11-12 GF 11-24 

11-13 GF Toxicity Estimates 11-26 

11-14 VX 11-27 

11-15 VX Toxicity Estimates 11-29 

11-16 Vx 11-30 

11-17 Vx Toxicity Estimates 11-31 

11-18 AC 11-32 



VII 



11-19 AC Toxicity Estimates 11-33 

11-20 CK 11-34 

11-21 CK Toxicity Estimates 11-35 

11-22 SA 11-36 

11-23 SA Toxicity Estimates 11-37 

11-24 HD 11-38 

11-25 HD Toxicity Estimates 11-40 

11-26 HN-1 11-41 

11-27 HN-1 Toxicity Estimates 11-43 

11-28 HN-2 11-43 

11-29 HN-2 Toxicity Estimates 11-45 

11-30 HN-3 11-46 

11-31 HN-3 Toxicity Estimates 11-48 

11-32 HT 11-48 

11-33 HT Toxicity Estimates 11-50 

11-34 L 11-50 

11-35 L Toxicity Estimates 11-53 

11-36 HL 11-54 

11-37 HL Toxicity Estimates 11-56 

11-38 PD 11-57 

11-39 PD Toxicity Estimates 11-58 

11-40 ED 11-59 

11-41 ED Toxicity Estimates 11-60 

11-42 MD 11-60 

11-43 MD Toxicity Estimates 11-62 

11-44 CX 11-63 

11-45 CX Toxicity Estimates 11-64 

11-46 BZ 11-65 

11-47 BZ Toxicity Estimates 11-66 

11-48 Correlation of Symptoms and Incapacitating 

Agent Family 11-68 

11-49 DF 11-69 

11-50 DF Toxicity Estimates 11-70 

11-51 QL 11-71 



VIM 



11-52 QL Toxicity Estimates 11-72 

11-53 OPA 11-72 

11-54 OPA Toxicity Estimates 11-73 

11-55 NE 11-74 

11-56 NE Toxicity Estimates 11-75 

11-57 NM (Containing Elemental Sulfur) 11-75 

11-58 NM Toxicity Estimates 11-76 

11-59 Other CW Agents 11-76 

lll-l List of Selected Military Chemical Compounds Ill-l 

111-2 CS 111-2 

111-3 CS Toxicity Estimates 111-3 

111-4 CR 111-4 

111-5 CR Toxicity Estimates 111-5 

111-6 OC 111-5 

111-7 OC Toxicity Estimates 111-7 

111-8 DM 111-7 

111-9 DM Toxicity Estimates 111-9 

111-10 DA 111-10 

111-11 DA Toxicity Estimates 111-11 

111-12 DC 111-12 

111-13 DC Toxicity Estimates 111-13 

111-14 Cl 2 111-13 

111-15 CI2 Toxicity Estimates 111-14 

111-16 CN 111-15 

111-17 ZnCl 2 111-17 

111-18 WP 111-18 

111-19 Ti0 2 111-19 

111-20 Synthetic Graphite 111-20 

111-21 SGF-2 111-21 

IV-1 List of Potential BW Agents IV-2 

IV-2 Animal and Plant Pathogens with Potential 

BW Applications IV-3 

V-l Accidents Involving Hazardous Substances V-2 

A-l Table of Equivalents A-l 



IX 



A-2 Table of Commonly Used Prefixes A-l 

B-l Temperature Conversions B-l 

C-l Periodic Table of the Elements C-l 

C-2 Chemical Elements and Symbols C-2 

D-l CWC Schedule 1 Chemicals D-l 

D-2 CWC Schedule 2 Chemicals D-2 

D-3 CWC Schedule 3 Chemicals D-3 

E-l CW Agent Precursor Chemicals: Uses and 

Equivalents E-l 

F-l Symbols for CW Agents and Military Chemical 

Compounds F-l 

G-l Physical Properties of Choking, Nerve, and Blood 

Agents G-2 

G-2 Physical Properties of Blister and 

Incapacitating Agents G-7 

G-3 Physical Properties of RCAs and Respiratory Irritants G-12 

G-4 Toxicity Estimates for CW Agents G-17 

G-5 Toxicity Estimates (Exposure Duration) for Military 

Chemical Compounds G-18 

G-6 Persistency of Selected CW Agents G-18 

H-l CG Profile Estimates (Lethal Dose, Inhalation/Ocular) H-l 

H-2 DP Profile Estimates (Lethal Dose, Inhalation/Ocular) H-l 

H-3 GA Profile Estimates (Lethal Dose, Inhalation/Ocular) H-l 

H-4 GA Profile Estimates (Lethal Dose, Percutaneous) H-2 

H-5 GA Profile Estimates (Severe Effects, Inhalation/Ocular) H-2 

H-6 GA Profile Estimates (Severe Effects, Percutaneous) H-2 

H-7 GA Profile Estimates (Threshold Effects, Percutaneous) H-3 

H-8 GA Profile Estimates (Mild Effects, Inhalation/Ocular) H-3 

H-9 GB Profile Estimates (Lethal Dose, Inhalation/Ocular) H-4 

H-10 GB Profile Estimates (Lethal Dose, Percutaneous) H-5 

H-ll GB Profile Estimates (Severe Effects, Inhalation/Ocular) H-5 

H-12 GB Profile Estimates (Severe Effects, Percutaneous) H-5 

H-13 GB Profile Estimates (Threshold Effects, Percutaneous) H-6 

H-14 GB Profile Estimates (Mild Effects, Inhalation/Ocular) H-6 

H-15 GD Profile Estimates (Lethal Dose, Inhalation/Ocular) H-7 



H-16 GD Profile Estimates (Lethal Dose, Percutaneous) H-8 

H-17 GD Profile Estimates (Severe Effects, Inhalation/Ocular) H-8 

H-18 GD Profile Estimates (Severe Effects, Percutaneous) H-8 

H-19 GD Profile Estimates (Threshold Effects, Percutaneous) H-9 

H-20 GD Profile Estimates (Mild Effects, Inhalation/Ocular) H-9 

H-21 GF Profile Estimates (Lethal Dose, Inhalation/Ocular) H-10 

H-22 GF Profile Estimates (Lethal Dose, Percutaneous) H-10 

H-23 GF Profile Estimates (Severe Effects, Inhalation/Ocular) ... H-ll 

H-24 GF Profile Estimates (Severe Effects, Percutaneous) H-ll 

H-25 GF Profile Estimates (Threshold Effects, Percutaneous) H-ll 

H-26 GF Profile Estimates (Mild Effects, Inhalation/Ocular) H-12 

H-27 VX Profile Estimates (Lethal Dose, Inhalation/Ocular) H-13 

H-28 VX Profile Estimates (Lethal Dose, Percutaneous) H-14 

H-29 VX Profile Estimates (Severe Effects, Inhalation/Ocular) ... H-14 

H-30 VX Profile Estimates (Severe Effects, Percutaneous) H-14 

H-31 VX Profile Estimates (Threshold Effects, Percutaneous) H-15 

H-32 VX Profile Estimates (Mild Effects, Inhalation/Ocular) H-15 

H-33 AC Profile Estimates (Lethal Dose, Inhalation/Ocular) H-16 

H-34 SA Profile Estimates (Lethal Dose, Inhalation/Ocular) H-16 

H-35 HD Profile Estimates (Lethal Dose, Inhalation/Ocular) H-17 

H-36 HD Profile Estimates (Lethal Dose, Percutaneous) H-17 

H-37 HD Profile Estimates (Severe Effects, Percutaneous) H-17 

H-38 HD Profile Estimates (Severe Effects, Ocular) H-18 

H-39 HD Profile Estimates (Mild Effects, Percutaneous) H-18 

H-40 HD Profile Estimates (Mild Effects, Ocular) H-18 

H-41 HN-1 Profile Estimates (Lethal Dose, Inhalation/Ocular)... H-20 

H-42 HN-1 Profile Estimates (Lethal Dose, Percutaneous) H-20 

H-43 HN-1 Profile Estimates (Severe Effects, Percutaneous) H-20 

H-44 HN-1 Profile Estimates (Severe Effects, Ocular) H-21 

H-45 HN-1 Profile Estimates (Mild Effects, Percutaneous) H-21 

H-46 HN-1 Profile Estimates (Mild Effects, Ocular) H-21 

H-47 HN-2 Profile Estimates (Lethal Dose, Inhalation/Ocular)... H-22 

H-48 HN-2 Profile Estimates (Lethal Dose, Percutaneous) H-22 

H-49 HN-2 Profile Estimates (Severe Effects, Percutaneous) H-22 



XI 



H-50 HN-2 Profile Estimates (Severe Effects, Ocular) H-23 

H-51 HN-2 Profile Estimates (Mild Effects, Percutaneous) H-23 

H-52 HN-2 Profile Estimates (Mild Effects, Ocular) H-23 

H-53 HN-3 Profile Estimates (Lethal Dose, Inhalation/Ocular)... H-24 

H-54 HN-3 Profile Estimates (Lethal Dose, Percutaneous) H-24 

H-55 HN-3 Profile Estimates (Severe Effects, Percutaneous) H-24 

H-56 HN-3 Profile Estimates (Severe Effects, Ocular) H-25 

H-57 HN-3 Profile Estimates (Mild Effects, Percutaneous) H-25 

H-58 HN-3 Profile Estimates (Mild Effects, Ocular) H-25 

H-59 HT Profile Estimates (Lethal Dose, Inhalation/Ocular) H-26 

H-60 HT Profile Estimates (Lethal Dose, Percutaneous) H-26 

H-61 HT Profile Estimates (Severe Effects, Percutaneous) H-26 

H-62 HT Profile Estimates (Severe Effects, Ocular) H-27 

H-63 HT Profile Estimates (Mild Effects, Percutaneous) H-27 

H-64 HT Profile Estimates (Mild Effects, Ocular) H-27 

H-65 L Profile Estimates (Lethal Dose, Inhalation/Ocular) H-28 

H-66 L Profile Estimates (Lethal Dose, Percutaneous) H-28 

H-67 L Profile Estimates (Severe Effects, Percutaneous) H-28 

H-68 L Profile Estimates (Severe Effects, Ocular) H-29 

H-69 L Profile Estimates (Mild Effects, Percutaneous) H-29 

H-70 L Profile Estimates (Mild Effects, Ocular) H-29 

H-71 HL Profile Estimates (Lethal Dose, Inhalation/Ocular) H-30 

H-72 HL Profile Estimates (Lethal Dose, Percutaneous) H-30 

H-73 HL Profile Estimates (Severe Effects, Percutaneous) H-30 

H-74 HL Profile Estimates (Severe Effects, Ocular) H-31 

H-75 HL Profile Estimates (Mild Effects, Percutaneous) H-31 

H-76 HL Profile Estimates (Mild Effects, Ocular) H-31 

H-77 PD Profile Estimates (Lethal Dose, Inhalation/Ocular) H-32 

H-78 CX Profile Estimates (Lethal Dose, Inhalation/Ocular) H-32 

H-79 DM Profile Estimates (Lethal Dose, Inhalation/Ocular) H-32 

1-1 Properties of Selected Biological Agents 1-2 



XII 



EXECUTIVE SUMMARY 



Potential Military Chemical/Biological Agents and Compounds 



Chapter I 
Introduction 

Chapter I briefly addresses the threat and the significant military aspects of 
chemical and biological agents and TIC. 



Chapter II 
Chemical Warfare Agents and Their Properties 

Chapter II provides information on chemical agents that might be encountered 
in the field. It discusses chemical agent physical characteristics and toxicity data of 
choking, nerve, blood, blister, and incapacitating agents. 



Chapter III 
Military Chemical Compounds and Their Properties 

Chapter III discusses military chemical compounds such as the riot control 
agents (RCAs). It provides physical and chemical characteristics and toxicity data 
for military chemical compounds. 



Chapter IV 
Biological Agents and Their Properties 

Chapter IV addresses general characteristics of biological agents (including 
toxins) and provides a summary of selected antipersonnel agents that may be 
employed in weapons systems. 



Chapter V 
Toxic Industrial Chemicals and Their Properties 

Chapter V addresses TIC and a summary of available TIC information sources. 



XIII 



PROGRAM PARTICIPANTS 

The following commands and agencies participated in the development of this publication: 

Joint 

Joint Requirements Office, 401 MANSCEN Loop, Suite 1309, Fort Leonard Wood, MO 
65473 

Army 

United States Army Chemical School, 401 MANSCEN Loop, Suite 1029, Fort Leonard 
Wood, MO 65473 

United States Army Edgewood Chemical and Biological Center, Aberdeen Proving Ground, 
MD 21040 

Marine Corps 

United States Marine Corps Combat Development Command, 3300 Russell Road, Suite 
318A, Quantico, VA 22134-5021 

Navy 

United States Navy Warfare Development Command, 686 Cushing Road, Sims Hall, 
Newport, RI 02841 

United States Navy Surface Warfare Development Group, 2200 Amphibious Drive, Norfolk, 
VA 23521 

Air Force 

HQ Air Force Doctrine Center, ATTN: D J, 155 North Twining Street, Maxwell AFB, AL 
36112-6112 

HQ Air Force Civil Engineer Support Agency, 139 Barnes Drive, Suite 1, Tyndall AFB, FL 
32403-5319 



XIV 



Chapter I 
INTRODUCTION 



1. Background 

The threat or use of CB weapons is a possible condition of future warfare and could 
occur in the early stages of war to disrupt United States (US) operations and logistics. In 
many of the regions where the US is likely to deploy forces, potential adversaries may use 
CB weapons. Potential adversaries may seek to counter US conventional military 
superiority using less expensive and more attainable, asymmetrical means. To meet this 
challenge, US forces must be properly trained and equipped to operate effectively and 
decisively in the face of NBC attacks. 1 Additionally, US forces could be confronted in an 
environment where TIC present a hazard to US forces. 2 

a. Use of CB Weapons. 3 Adversaries may employ CB agents and other toxic 
materials to achieve specific effects. In addition to the physical effects, there exist 
psychological effects, both in the immediate target area and in other vulnerable areas that 
may be potential targets. 

(1) Chemical agents have effects that can be immediate or delayed, can be 
persistent or nonpersistent, and can have significant physiological effects. While relatively 
large quantities of an agent are required to ensure an area remains contaminated over 
time, small-scale selective use that exploits surprise can cause significant disruption and 
may have lethal effects. 

(2) Biological agents can produce lethal or incapacitating effects over an 
extensive area and can reproduce. The delayed onset of symptoms and detection, 
identification, and verification difficulties for biological agents can also confer important 
advantages to adversaries who decide to use biological agents. 

(3) The means available to adversaries for delivery of CB weapons range from 
specially designed, sophisticated weapon systems developed by nations to relatively 
inefficient improvised devices employed by terrorists and other disaffected individuals and 
groups. 

b. US Policy. 3 This paragraph contains brief descriptions of treaty, legal, and 
policy strictures on chemical and biological warfare (CBW). 

(1) The Protocol for the Prohibition of the Use in War of Asphyxiating, 
Poisonous or Other Gases, and of Bacteriological Methods of Warfare," also known as the 
Geneva Protocol of 1925, prohibits chemical and bacteriological methods of warfare. Most 
parties interpret the protocol as a prohibition only of the first use of these agents in war. It 
did not ban the development, production, or stockpiling of these weapons. In 1974, the US 
Senate gave advice and consent to ratification of this protocol, subject to the reservation 
that the US would not be bound by the provisions with respect to an enemy state or its 
allies who fail to respect the prohibitions of the protocol. On 22 January 1975, the US 
ratified the protocol subject to this reservation. The protocol entered into force for the US 
on 10 April 1975. The relevance of the Geneva Protocol is largely superseded by the more 



1-1 



restrictive Convention on the Prohibition of the Development, Production, Stockpiling, and 
Use of Chemical Weapons and on their Destruction (also known as the Chemical Weapons 
Convention [CWCJ and by the Convention on the Prohibition of Bacteriological and Toxic 
Weapons (also known as the Biological Weapons Convention [BWCJ) summarized below. 

(2) The Presidential Statement on Chemical and Biological Weapons, 25 
November 1969, renounced the US use of lethal biological agents and weapons and confined 
biological research to defensive measures such as immunization and safety. Under the 
terms of the BWC, parties undertake not to develop, produce, stockpile, or acquire biological 
agents or toxins "of types and in quantities that have no justification for prophylactic, 
protective and other peaceful purposes," as well as weapons and means of delivery. The 
BWC does not establish a specific verification regime. The US ratified the BWC on 29 
March 1975. 

(3) Executive Order No. 11850, 8 April 1975, Renunciation of Certain Uses in 
War of Chemical Herbicides and Riot Control Agents, renounced first use of herbicides in 
war (except for specified defensive uses) and first use of RCAs in war except for defensive 
military modes to save lives. 

(4) The CWC, which entered into force on 29 April 1997, bans the development, 
production, acquisition, stockpiling, transfer, or use of chemical weapons. It provides for 
the destruction of all chemical weapons stocks within 10 years after entry into force. It 
contains a vigorous challenge regime to ensure compliance. The US ratified the CWC on 25 
April 1997. 

2. Threat 

a. Changes. 4 Countries with chemical weapons programs are adding agents and 
more sophisticated delivery systems. Similarly, the sophistication of CBW capabilities is 
increasing. Proliferation of weapons technology, precision navigation technology, and CBW 
technology in developing nations presents the US with a complicated national security 
challenge. Intelligence efforts include collection and analysis of nations' dual-use, CB 
industrial capabilities, and development of the indications and warning of adversarial use 
of dual-use capabilities. 

b. Challenges. The US faces a number of regional proliferation challenges. Many 
of these are detailed in the January 2001 report published by the Office of the Secretary of 
Defense (OSD), Proliferation: Threat and Response. At least 25 countries now possess — or 
are in the process of acquiring and developing — capabilities to inflict mass casualties and 
destruction: NBC weapons or the means to deliver them. 5 

c. Proliferation. 4 Proliferation of CBW technology also raises several important 
issues. Various nations could export a wide array of chemical products, including 
Australian group-controlled items to numerous countries of proliferation concern. The 
controlled items include specific chemical agent precursors, pathogens with biological 
warfare (BW) applications, and dual-use equipment that can be used in both CBW 
programs. 

d. Increases in Proliferation. 4 In the next several years, the threat from the 
proliferation of CBW may increase. This could result from the development of CB agents 
that are more difficult to detect and from the adoption of more capable delivery systems. 
States with existing programs may master the production processes for complete weapons 
development and will be less dependent on outside suppliers. 



1-2 



(1) Any nation with the political will and a minimal industrial base could 
produce CBW agents suitable for use in warfare. Efficient weaponization of these agents, 
however, does require design and production skills usually found in countries that possess a 
munitions development infrastructure or access to such skills from cooperative sources. 

(2) On the other hand, almost any nation or group could fabricate crude agent 
dispersal devices. Such weapons might be capable of inflicting only limited numbers of 
casualties; nevertheless, they could have significant operational repercussions due to the 
psychological impact created by fears of CBW agent exposure. 4 

(3) Genetic engineering gives BW developers the tools to pursue agents that 
could defeat the protective and treatment protocols of the prospective adversary. 
Genetically engineered microorganisms also raise the technological hurdle that must be 
overcome to provide for effective detection, identification, and early warning of BW attacks. 

(4) Numerous characteristics need to be controlled for a highly effective BW 
agent. Historically, the accentuation of one characteristic often resulted in the attenuation 
of one or more other characteristics, possibly even rendering the modified agent ineffective 
as a weapon. Advances in biotechnology, genetic engineering, and related scientific fields 
provide ever-increasing potential to control more of these factors, possibly leading to an 
enhanced ability to use BW agents as battlefield weapons. 

e. Novel BW Agents. 1 Advances in biotechnology and genetic engineering may 
facilitate the development of potentially new and more deadly BW agents. The ability to 
modify microbial agents at a molecular level has existed since the 1960s, when new genetic 
engineering techniques were introduced, but the enterprise tended to be slow and 
unpredictable. With today's techniques, infectious organisms can be modified to bring 
about disease in different ways. The current level of sophistication for many biological 
agents is low, but there is enormous potential — based on advances in modern molecular 
biology, fermentation, and drug delivery technology — for making more sophisticated 
weapons. The BW agents may emerge in two likely categories: man-made manipulations of 
classic BW agents and newly discovered or emerging infectious diseases. An example of a 
recent new pathogen (though not necessarily ideal BW agents) includes streptococcus 
pneumonia S23F, a naturally occurring strain of pneumonia resistant to at least six of the 
more commonly used antibiotics. 

(1) The potential types of novel biological agents that could be produced 
through genetic engineering methodologies are listed below. Each of these techniques seeks 
to capitalize on the extreme lethality, virulence, or infectivity of BW agents and exploit this 
potential by developing methods to deliver more efficiently and to control these agents on 
the battlefield. 

(a) Benign microorganisms genetically altered to produce a toxin, venom, 
or bioregulator. 

(b) Microorganisms resistant to antibiotics, standard vaccines, and 
therapeutics. 

(c) Microorganisms with enhanced aerosol and environmental stability. 

(d) Immunologically altered microorganisms able to defeat standard 
identification, detection, and diagnostic methods. 

(e) Combinations of the above four types with improved delivery systems. 



1-3 



(2) The future likelihood of infectious agents being created for BW purposes 
will be influenced by technological trends such as — 

(a) Genetically engineered vectors in the form of modified infectious 
organisms may become increasingly available as medical tools and techniques become more 
widely available. 

(b) Strides will be made in the understanding of infectious disease 
mechanisms and in microbial genetics that are responsible for disease processes. 

(c) An increased understanding of the human immune system function 
and disease mechanisms will shed light on the circumstances that cause individual 
susceptibility to infectious disease. 

(d) Vaccines and antidotes will be improved over the long term, perhaps 
to the point where classic BW agents will offer less utility as a means of causing casualties. 

(e) Many bioengineering companies (both US and foreign) now sell all-in- 
one kits to enable researchers to perform recombinant deoxyribonucleic acid (DNA) 
experiments. The availability of free online gene sequence databases and analytic software 
over the Internet further amplifies and disseminates this capability. It is now possible to 
transform relatively benign organisms to cause harmful effects. 

3. Militarily Significant Aspects of Toxic Chemical Agents 

a. Classification. A toxic chemical agent is any chemical which, through its 
chemical action on life processes, can cause death, temporary incapacitation, or permanent 
harm to humans or animals. 6 For the purpose of this manual, chemical agents are further 
divided into chemical warfare (CW) agents and military chemical compounds. The terms 
"persistent" and "nonpersistent" describe the time chemical agents remain in an area and 
do not classify the agents technically. 

(1) CW Agents. The CW agents are toxic chemicals and their precursors 
prohibited under the CWC. These agents include choking, nerve, blood, blister, and 
incapacitating agents. Their physiological actions are as follows: 

(a) Choking Agents. 7 Choking agents cause damage to the lungs, 
irritation to the eyes and the respiratory tract, and pulmonary edema ("dry-land 
drowning") . 

(b) Nerve Agents. Nerve agents inhibit cholinesterase (ChE) enzymes. 
This inhibition permits acetylcholine (ACh), which transmits many nerve impulses, to 
collect at its various sites of action. 7 The body's muscles and glands become overstimulated 
due to excessive amounts of ACh. At sufficient doses, this can lead to an inability of the 
body to sustain breathing. 

(c) Blood Agents. 7 The blood transports these agents to all body tissues. 
Hydrogen cyanide (AC) and cyanogen chloride (CK) are cellular poisons, and they disrupt 
the oxidative processes used by the cells. 7 Arsine (SA) is different. It causes hemolysis of 
the red blood cells. 8 The central nervous system (CNS) is especially vulnerable to lack of 
oxygen regardless of the etiology, and respiratory and cardiovascular collapse resulting 
from AC and CK poisoning. In the case of SA poisoning, the proximal cause of death is 
myocardial failure. 



1-4 



(d) Blister Agents (Vesicants). Blister agents are noted for producing 
reddening and blistering of the skin, but the eyes and respiratory tract are more sensitive 
than the skin. Eye exposure results in reddening of the eyes and temporary blindness or 
permanent effects. Inhaled mustard damages mucous membranes and the respiratory 
tract. 7 

(e) Incapacitating Agents. 9 Used in a military context, incapacitation is 
understood to mean inability to perform one's military mission. Since missions vary, for the 
purpose of this manual, incapacitation means the inability to perform any military task 
effectively. An incapacitating agent is an agent that produces temporary physiological or 
mental effects, or both, which will render individuals incapable of concerted effort in the 
performance of their assigned duties. Medical treatment is not essential but can facilitate a 
more rapid recovery. 7 

(2) Military Chemical Compounds. Military chemical compounds are less toxic 
and include materials such as respiratory irritant agents, RCAs, smoke and obscurants, 
and incendiary materials. The term excludes CW agents. Their physiological actions are as 
follows: 

(a) RCAs (Lacrimators). The RCAs are chemicals that rapidly produce in 
humans sensory irritation or disabling physical effects which disappear within a short time 
following termination of exposure. 6 They are local irritants that, in very low 
concentrations, act primarily on the eyes, causing intense pain and tearing. At high 
concentrations they irritate the respiratory tract and the skin. They sometimes cause 
nausea and vomiting. 

(b) Respiratory Irritant Agents. These agents were previously called 
vomiting agents. Their primary action is irritation of the respiratory tract. 10 In addition, 
these agents cause lacrimation (tearing), irritation of the eyes, uncontrollable coughing, 
sneezing, nausea, and a general feeling of bodily discomfort. Usually symptoms disappear 
in 20 minutes to 2 hours, leaving no residual injury. 7 

b. Duration of Effectiveness. Several factors determine the time a chemical agent 
remains effective. These include, but are not limited to, the method of dissemination, 
weather and terrain conditions, and the physical and chemical properties of the agent. 

(1) Method of Dissemination. 11 Chemical agents are usually disseminated in 
the field in the form of vapors (gases), aerosols, or liquids. When a chemical agent is 
disseminated as a vapor from a bursting munition, initially the cloud expands, grows cooler 
and heavier, and tends to retain its form. Aerosols are finely divided liquid and/or solid 
substances suspended in the atmosphere and behave in much the same manner as 
vaporized agents. Liquid agents can be absorbed (soaked into) and adsorbed (adhered to) 
by surfaces. They can then be evaporated or desorbed (off-gas) from surfaces, causing a 
vapor hazard. 

(2) Weather and Terrain Conditions. 11 Many weather factors and terrain 
conditions influence the duration of effectiveness of chemical agents. Most important 
weather factors include temperature, temperature gradient, wind speed, relative humidity, 
and precipitation. Important terrain conditions include vegetation, soil, and terrain 
contours. 

(3) Physical Properties. Some of the important physical properties are vapor 
density, vapor pressure (VP), volatility, freezing point (FP), and melting point (MP). Vapor 



1-5 



density determines whether the agent is lighter or heavier than air, thus determining 
whether the agent will settle to low areas or float away and dissipate in the atmosphere. 
Vapor pressure is used to determine the volatility of an agent. The volatility has an effect 
upon the vapor concentration. It also affects the duration of an agent hazard after 
dissemination. The boiling and freezing points of chemical agents influence their 
operational use and the means of disseminating them. See Appendix A for information on 
table of equivalents and commonly used prefixes, Appendix B for information on 
temperature conversions, and Appendix C for the periodic table of elements. See Chapter II 
for definitions of selected physical properties. 

(4) Chemical Properties. The chemical properties of an agent include its 
stability and reactivity with water and other substances. See Chapter II for definitions of 
selected chemical properties. 

c. Potency and Physiological Actions. Factors that contribute to the adverse 
human health effects of chemical agents include toxicity, route of exposure (ROE), dosage, 
exposure duration, minute volume (MV), temperature, endpoint, physiological stressors, 
rate of detoxification (ROD), and rate of action (ROA). Note that not all factors are 
applicable to all exposure scenarios. For example, MV is not applicable to a percutaneous 
liquid exposure. Dosages are given for a 70-kilogram (kg) male with an MV of 15 liters per 
minute (L/min). Additional toxicological data are required to determine if the toxicity 
estimates can be applied to women. Emphasis is placed on acute toxic effects. Acute toxic 
effects are those occurring within moments to a few days of the toxic exposure. The toxicity 
estimates provided are not applicable to the general population. 10 ' 12 - 13 

NOTE: Occupational health guidelines for the evaluation and control of 
occupational exposure to nerve and blister agents is promulgated separately by 
the US Army Surgeon General in DA Pamphlets 40-8 and 40-173. These references 
define the medical surveillance program for personnel who support chemical 
demilitarization operations. 

d. CWC Chemicals. Appendix D contains the list of toxic chemicals, groups of 
chemicals, and precursors subject to the CWC. The examples given in Appendix D are not 
all-inclusive. There are, by conservative estimates, 25,000 or more chemicals subject to the 
CWC regulation — listing each chemical by name is not practical. 14 Chemicals covered 
under the CWC are divided into three categories as follows: 

(1) Schedule 1 chemicals (See Table D-l, page D-l) have little or no use in 
industrial and agricultural industries. They pose a high risk to the object and purpose of 
the CWC by virtue of their high potential for use in activities prohibited under the CWC. 14 

(2) Schedule 2 chemicals (See Table D-2, page D-2) may be useful in the 
production of chemical weapons; however, they also have legitimate uses in other industrial 
areas. They pose a significant risk to the object and purpose of the CWC. 14 

(3) Schedule 3 chemicals (See Table D-3, page D-3) have legitimate uses in 
industrial areas and pose a risk to the object and purpose of the CWC. 14 

e. Dual-Use Precursors. Precursors for CW agents also have civil uses in industrial 
and agricultural industries (see Appendix E). 

f. CW Agents and Other Military Chemical Compounds. See Appendix F for the 
symbols of CW agents and other military chemical compounds. See Appendix G for a 



1-6 



consolidation of the information given in the chemical agent tables and toxicity tables in 
Chapters II and III. 

NOTE: See information in Chapters II, III, and Appendix H for detailed 
information on toxicity of CW agents and military chemical compounds. 

g. Agent Mixtures. Mixing chemical agents with each other or with other materials 
can alter the characteristics and effectiveness of the agents. Mixtures may lower the 
freezing point, increasing agent effectiveness over a wider temperature range. The addition 
of thickeners or thinners to agents will increase or decrease persistency: for example, 
soman (GD) mixed with thickeners will increase persistency; RCAs mixed with thinners 
will decrease persistency. In addition to changing the physical properties, mixing agents 
together will create special problems through their physiological effects. These problems 
can produce difficulty in identification, immediate and delayed effects, or contact and vapor 
hazards occurring simultaneously. Some mixtures would make it difficult to maintain the 
seal of the protective mask. Mixing some agents can also increase the toxic effects, either 
by a synergistic effect or by an improved absorption through the skin. 

4. Militarily Significant Aspects of Biological Agents 

a. Classification. A biological agent is a microorganism that causes disease in 
personnel, plants, or animals or causes the deterioration of material. 6 Biological agents can 
be classified as pathogens, toxins, bioregulators, or prions. 

(1) Pathogens. Pathogens are disease-producing microorganisms, 6 such as 
bacteria, rickettsiae, or viruses. Pathogens are either naturally occurring or altered by 
random mutation or recombinant DNA techniques. 

(2) Toxins. Toxins are poisons formed as a specific secreting product in the 
metabolism of a vegetable or animal organism, as distinguished from inorganic poisons. 
Such poisons can also be manufactured by synthetic processes. 6 Toxins are produced by a 
variety of organisms, including microbes, snakes, insects, spiders, sea creatures, and 
plants. 15 

(3) Bioregulators. Bioregulators include biochemical compounds that regulate 
cell processes and physiologically active compounds such as catalysts and enzymes. 
Although they can be found in the human body in small quantities, introduction of large 
quantities can cause severe adverse effects or death. 15 

(4) Prions. Prions are proteins that can cause neurodegenerative diseases in 
humans and animals. 16 Proteins have a unique, genetically defined amino acid sequence 
that determines their specific shapes and functions. Normal cell proteins have the same 
amino acid building blocks but they fold differently than prions. When prions enter brain 
cells, they apparently convert normal proteins into prions. Ultimately, the infected brain 
cells die and release prions into the tissue. These prions enter, infect, and destroy other 
brain cells. Prions entered the public's consciousness during the mad cow epidemic that hit 
England in 1996. 17 Transmission of the prions from cows to man is suspected to cause 
human illness. There are no known therapies effective against prions. 18 

b. Uses. Biological agents can be disseminated and used against personnel, 
animals, plants, or material. Food and industrial products can be rendered unsafe or unfit 
for use by contamination or by the effects resulting from contamination with biological 
agents. The US military forces are deployed throughout the world. Associated with the 



1-7 



movement of troops are risks of introduction of exotic agricultural pests and animal disease 
agents through soil contamination and transportation of regulated items such as fruits, 
vegetables, meat, and dairy products, other food items, and animal products (e.g., trophies). 
The United States Department of Agriculture (USDA), Animal and Plant Health Inspection 
Service (APHIS) oversees the entry of cargo, personnel, equipment, personal property, mail, 
and their means of conveyance into the US. 19 (See Appendix I for selected properties of 
some biological agents.) 

(1) Antipersonnel. Biological antipersonnel agents are those that are effective 
directly against humans. The threat would select these agents on the basis of the agents' 
ability to cause death or disability. Potential biological antipersonnel agents include toxins, 
bacteria, rickettsiae, viruses, and toxins. 

(2) Antianimal. Biological antianimal agents are those that could be employed 
against animals to incapacitate or destroy them through disease. The purposeful spreading 
of infectious agents that attack cattle or other domestic animals can lead to serious 
consequences for a country's food supply or export of animal products (hides, wool, fats, and 
biological medicinal products such as adrenalin, insulin, pituitary extracts, cortisone, 
vaccines, and antisera). 20 See Appendix J. 

(3) Antiplant. Biological antiplant agents are organisms that cause disease or 
damage to plants. These agents may be used intentionally by an enemy to attack food or 
economically valuable crops, thereby reducing a nation's ability to resist aggression. 20 See 
Appendix K. 

(4) Antimaterial. Antimaterial agents are organisms that degrade or break 
down some item of material. For example, fungi may damage fabrics, rubber products, 
leather goods, or foodstuffs. Some bacteria produce highly acidic compounds that cause 
pitting in metals; these agents could create potential problems with stockpiled material. 
Some bacteria can use petroleum products as an energy source and cause residues that 
might clog fuel or oil lines. 20 

c. Duration of Effectiveness. The duration of effectiveness of a biological agent 
refers to the persistency of the agent in the environment. It depends on the characteristics 
of the agent and environmental factors. 3 

(1) Biological agent characteristics such as encapsulation (natural, such as 
bacterial spores, or manmade protective coverings), addition of dyes to the spray fluid, or 
possibly genetic engineering (of pathogens) may protect some agents from sunlight and 
other destructive natural forces. 3 Bacteria that are resistant to environmental extremes 
frequently produce spores to allow survival during adverse conditions. Spore formation is 
not a method of reproduction inasmuch as each vegetative cell forms only a single spore and 
each spore germinates to form a single vegetative cell. The bacterium (vegetative cell) 
makes a copy of its DNA. The DNA becomes surrounded by a series of membranes that 
accumulate calcium, dipicolinic acid (heat-resistant factor), and protein layers. The 
resistant spore might remain dormant for years without requiring nutrients or water and 
might survive under extreme ranges of temperature. When conditions become favorable, 
the spore develops into an actively growing vegetative cell. 21 

(2) Ultraviolet (UV) radiation, relative humidity, wind speed, and temperature 
gradient are important weather factors in determining duration of effectiveness. 



1-8 



d. Methods of Dissemination. 22 Biological agents may be disseminated as aerosols, 
liquid droplets (toxins only), or dry powders. See Appendix L for additional information on 
dissemination of biological agents. 

(1) Biological agents may be delivered in either wet or dry form. Dry powders 
composed of very small particles tend to have better dissemination characteristics and have 
advantages in storage. Dried agents require an increased level of technological 
sophistication to produce, although freeze-drying and spray-drying technologies have been 
available in the industry for a number of years. 

(2) The BW agents might be released against our forces or against civilian 
populations by means of sprays, explosive devices, and contamination of food and water. 
Most commonly, delivery methods use aerosolized agents. 

(a) A BW agent can be released as a line source. A line source would be 
released perpendicular to the direction of the wind, upwind of the intended target area. 

(b) A second type of aerosol source is a point source, which is a stationary 
device for aerosolization of the agent, such as a stationary sprayer. A modified point source 
would be a group of spray devices, such as specially designed bomblets dispersed in a 
pattern on the ground or a missile or artillery shell designed to release such bomblets. 

e. Physiological Aspects. Employment considerations for BW agents include the 
following: 

(1) ROE. The important portals of entry are the respiratory tract, the exposed 
mucosal surfaces (moist surfaces of nose, mouth, and eyes), and the digestive tract. 23 In a 
biological attack the respiratory route would be the primary route of entry. 3 The 
respiratory system is much more susceptible to penetration. The body is more resistant to 
invasion by microorganisms through the skin; however, penetration across the skin can 
occur. This is particularly true of abraded (broken) surfaces and some toxins such as 
mycotoxins. 23 Toxins absorbed through the respiratory tract can produce signs and 
symptoms different from those acquired through natural occurrence. 24 For example, 
staphylococcal enterotoxin B when ingested in food causes acute gastrointestinal (GI) 
illness; however, when delivered via aerosol to the respiratory tract, it produces respiratory 
disease. 23 Personnel can encounter biological agents by natural routes, such as in water 
and food or by vectors. 

(2) Dosage. The BW agents are inherently more toxic than CW nerve agents 
on a weight-for-weight basis and can potentially provide broader coverage per pound of 
payload than CW agents. 15 

(a) Infective Dose. 25 The infectivity of an agent reflects the relative ease 
with which microorganisms establish themselves in a host species. Pathogens with high 
infectivity cause disease with relatively few organisms. 

(b) Lethal Dose. Some pathogens produce toxins that can result in 
disease (for example, anthrax, botulinum, cholera, diphtheria, and typhus). The extreme 
toxicity of many toxins causes the lethal dose to be much smaller than that of chemical 
agents. Hence, units of micrograms (|ag) or even nanograms (ng) may be used instead of 
milligrams (mg) in expressing toxicity. Human toxicity estimates are based on animal 
data, and the ROE for the animals is not always what would be expected on the battlefield. 



1-9 



Some human toxicity data are based on accidental contact, ingestion, or inhalation of these 
natural poisons. 

(3) ROA. The rate of reaction to toxins varies widely. Rapid-acting toxins 
generally incapacitate within minutes. Delayed-acting agents may take several hours to 
days to incapacitate. The time for maximum effects for pathogens is normally more than 24 
hours (unless the pathogen produces a toxin). However, the incubation periods of 
microorganisms used in BW may be far shorter than those expected by examining the 
natural disease. 

f. Requirements for a Weaponized BW Agent. 22 The key factors that make a 
biological agent suitable for an attack include availability or ease of production in sufficient 
quantity; the ability to cause either lethal or incapacitating effects in humans at doses that 
are achievable and deliverable; appropriate particle size in aerosol; ease of dissemination; 
stability (while maintaining virulence) after production in storage, weapons, and the 
environment; and susceptibility of intended victims with nonsusceptibility of friendly 
forces. 

(1) Availability or Ease of Production. Many replicating agents (bacteria and 
viruses) can be produced in large quantities with modern fermentation and viral production 
technologies. Some toxins, like ricin, are widely available because their source in nature is 
ubiquitous and the process necessary to harvest the toxin is technically straightforward. 
On the other hand, some replicating agents are very difficult to grow in quantity, and many 
toxins are produced in nature in such low quantities that harvesting them is impractical 
(shellfish toxins are a good example). 

(2) Incapacitation and Lethality. BW agents are likely to be selected for their 
ability to either incapacitate or kill the human targets of the attack. A BW agent does not 
necessarily have to be lethal to be useful as a military weapon. An agent such as 
Venezuelan equine encephalitis (VEE) virus could cause incapacitation among large 
numbers of unit personnel. If lethality is desired, agents such as anthrax have high case 
fatality rates once infection is established in unimmunized hosts. 

(3) Appropriate Particle Size in Aerosol. An effective weaponized BW agent is 
of a particle size that would allow it to be carried for long distances by prevailing winds and 
inhaled deeply into the lungs of the unsuspecting victims. The size range of particles that 
meets both of these conditions is 1 to 5 microns in diameter. Particles larger than this 
would either settle out into the ground or more likely be filtered out in the upper 
respiratory tract of those who inhale them. Particles in this size range are invisible to the 
human eye; thus, a cloud of such particles would not generally be detected by those 
attacked, even if such a cloud were to be carried through their position. It is worth noting, 
however, that particles outside this size range are still dangerous and able to cause deadly 
illnesses, even though their transmission efficiency is less. 

(4) Ease of Dissemination. An effective weaponized BW agent is easily 
disseminated in the open air by using off-the-shelf devices such as industrial sprayers or 
other types of aerosol-producing devices. These could be mounted on an airplane, boat, car, 
or other moving vehicle, or even placed in a stationary position. An alternative method 
would be to disseminate the agent in an enclosed space (e.g., a building) where it could 
more efficiently infect or intoxicate humans living or working in the area. 



1-10 



(5) Stability after Production. Once an adversary produces a BW agent in 
quantity, it must be fairly stable — either in bulk storage or once put into a weapon or 
delivery system. It must, therefore, retain its viability and virulence or toxicity during 
production, storage, transportation, and delivery. 

(6) Susceptibility and Nonsusceptibility. An effective BW agent is one to which 
the target force is known to be susceptible (i.e., not immunized against), but to which the 
adversary possesses high levels of immunity, usually via vaccination. 

5. Militarily Significant Aspects of Toxic Industrial Chemicals 

a. Classification. The TIC are chemicals that are toxic to plants, animals, or 
humans. 

b. Uses. The TIC are found in abundance in all countries, and are used in chemical 
manufacturing processes, agriculture (pesticides), water treatment (chlorination), and 
many other areas. Each year, more than 70,000 different chemicals amounting to billions 
of tons of material are produced, processed, or consumed by the global chemical industry. A 
large portion of these chemicals may exhibit characteristics or be sufficiently hazardous to 
be a threat in a military situation. 2 

c. Characteristics of TIC. The TIC of military concern may exist as solids, liquids, 
or gases. For many cases, release of a TIC may involve a change of the state of the 
chemical, therefore making protection difficult. Like CW agents, TIC include many lethal 
compounds. 

(1) Toxicity. Many TIC, due to their toxicity, can cause incapacitation or 
death. 

(2) Corrosiveness. Many TIC are highly corrosive. Special equipment 
containers and procedures are necessary to ensure safe handling. 

(3) Flammability. Many TIC are highly flammable and present a major fire 
hazard. 

(4) Explosiveness. Unlike CW agents, TIC can be highly explosive and present 
a serious threat when handled. 

(5) Reactivity. Many TIC react violently with water or other materials, and 
thus present dangers upon contact with other materials, including air. 

(6) Byproducts. When burned, mixed, or exploded, many TIC produce 
additional highly toxic byproducts. 

(7) Quantities available. The sheer volume and widespread availability of TIC 
present a serious danger in the event of a release. 

d. Duration of Effectiveness. A number of factors determine the amount of time a 
TIC would present a danger after release. Factors include the physical properties of the 
TIC as well as weather, terrain, and conditions at the release site. These factors affect TIC 
in the same manner as that for chemical agents. 3 

e. Physiological Aspects. Exposure to TIC affects the body in a variety of ways. 
Generally, they disrupt bodily functions. The effects are dependent on the routes of entry, 
toxicity of the chemical, and the concentration to which exposed. 



1-11 



(1) ROE. The TIC can enter the body through inhalation, ingestion, dermal 
absorption, or a combination of these methods. The primary concern for exposure is that of 
the inhalation of a TIC as a gas. 2 

(2) Exposure Concentration and Levels of Concern. The type and seriousness 
of effects from exposure to TIC, like any chemical is dependent upon the concentration and 
length of time one is exposed. This concentration and time relationship is unique to every 
chemical. The dosages of TIC are expressed in parts per million (ppm). In general, TIC 
tend to be at least one order of magnitude less potent than nerve agents and tend not be 
rapidly lethal in small quantities. Standards have been developed for industry for different 
exposure scenarios. 

(a) Immediately Dangerous to Life and Health (IDLH): 24 The definition of 
IDLH that was derived during the Standards Completion Program (SCP) was based on the 
Mine Safety and Health Administration (MSHA) definition stipulated in 30 CFR 11.3(t). 
The purpose for establishing an IDLH value in the SCP was to ensure that a worker could 
escape without injury or irreversible health effects from an IDLH exposure in the event of 
the failure of respiratory protection equipment. The highly reliable breathing apparatus 
providing maximum worker protection was permitted. In determining IDLH values, the 
ability of a worker to escape without loss of life or irreversible health effects was considered 
along with severe eye or respiratory irritation and other deleterious effects (e.g., 
disorientation or lack of coordination) that could prevent escape. As a safety margin, the 
SCP IDLH values were based on the effects that might occur as a consequence of a 30- 
minute exposure. However, the 30-minute period was not meant to imply that workers 
should stay in the work environment any longer than necessary. In fact, every effort should 
be made to exit immediately. 

(b) Refer to the United States Army Center for Health Promotion and 
Preventive Medicine (USACHPPM) Technical Guide 230, Chemical Exposure Guidelines for 
Deployed Military Personnel, for obtaining the military exposure guidelines for assessing 
exposure concentrations for TIC. 

f. TIC Hazard Assessment. As part of the IPB process, a planner must assess the 
likelihood of a release or exposure as well as the actual TIC material. Some example 
considerations are 3 — 

(1) Accidents in civilian operations significantly increase when technically 
trained personnel flee an area, such as a combat zone (CZ). Civilian personnel remaining 
may be pressured to operate equipment beyond their training/technical expertise in a area 
of combat. 

(2) Pipelines can offer a very attractive target for terrorists because actions can 
be planned well in advance of execution and pipelines do not rely on shipping or 
transportation scheduled. 

(3) Storage yards, ports, airfields and rail yards often contain significant 
amounts of transiting TIC. This not only presents opportunities for improvised use against 
US forces, but also presents increased possibility of accidents and targets for those who 
want to destroy the TIC (such as ammunition precursor chemicals). 

g. Pesticides. Large stockpiles of obsolete pesticides have been accumulated in 
virtually all developing countries over periods sometimes exceeding four decades. 28 The 
term "pesticides," as used by US forces include insecticides, rodenticides, fungicides, and 



1-12 



herbicides. The health effects of pesticides depend on the type of pesticide. Some, such as 
the organophosphates and carbamates, affect the nervous system. Others may irritate the 
skin or eyes. Some pesticides may be carcinogens. Others may affect the hormone or 
endocrine system in the body. 29 The US Environmental Protection Agency (EPA) has 
recognized the dangers of many pesticides and publishes lists of those pesticides that are 
either banned or severely restricted in their use. Applicable service personnel (e.g., Army 
preventive medicine (PVNTMED), Air Force civil engineering, public health) can provide 
information on specific pesticides that could be used in specific areas of operation (AOs). 



1-13 



NOTES 

1 Office of the Secretary of Defense, Proliferation: Threat and Response, ISBN: 0-16-042727- 
4, US Government Printing Office, November 1997. 

2 A.K. Steumpfle et al., Final Report of International Task Force-25: Hazard From Toxic 
Industrial Chemicals, March 18, 1996. 

3 Joint Publication 3-11, Joint Doctrine of Operations in NBC Environment, 11 July 2000. 

4 DOD Chemical and Biological Defense Program Annual Report to Congress, Vol. I, April 
2002. 

5 Office of the Secretary of Defense, Proliferation: Threat and Response, US Government 
Printing Office, January 2001. 

6 Joint Publication 1-02, Department of Defense Dictionary of Military and Associated Terms, 
as amended through 05 June 2003. 

7 FM 8-285/Navy Medical (NAVMED) P-5041/Air Force Joint Manual (AFJMAN) 44- 
149/Fleet Marine Force Manual (FMFM) 11-11, Treatment of Chemical Agent Casualties 
and Conventional Military Chemical Injuries, 22 December 1995. 

8 L. Fishbein and S. Czerczak, Concise International Chemical Assessment Document 47: 
Human Health Aspects, WHO, 2002. 

9 Brigadier General (BG) Russ Zajtchuck, et al. (eds.), Textbook of Military Medicine: 
Medical Aspects of Chemical and Biological Warfare, Office of the Surgeon General, 1997, 
Chapter 11, "Incapacitating Agents. " 

10 Sharon Reutter et al., Review and Recommendations for Human Toxicity Estimates for 
FM 3-11.9, ECBC-TR0349, September 2003. 

n FM 3-6/FMFM 7-11-H/Air Force Manual (AFM) 105-7, Field Behavior of NBC Agents 
(Including Smoke and Incendiaries), 3 November 1986. 

12 Jeffrey H. Grotte and Lynn I Yang, Report of the Workshop on Chemical Agent Toxicity for 
Acute Effects: Institute for Defense Analyses, May 11-12, 1998, IDA Document D-2176, June 
2001. 

13 Anna Johnson-Winegar, PhD, Assistant to the Secretary of Defense, Memorandum, 
Subject: Interim Certification of Chemical and Biological Data, December 27, 2001. 

14 Federal Register, Department of Commerce, Bureau of Export Administration, "15 CFR Part 
710 et al., Chemical Weapons Convention Regulations; Final Rule," December 30, 1999. 

15 Office of the US President, The Biological and Chemical Warfare Threat, 1999. 

16 Centers for Disease Control and Prevention (CDC), Office of Health and Safety (OHS), 
"BMBL Section VII: Agent Summary Statements, Section VII-D: Prions," 17 June 1999, 
http://www.cdc.gov/OD/OHS/BIOSFTY/bmbl4/bmbl4s7d.htm , 19 August 2003. 

17 Ruth Levy Guyer, "Research in the News: Prions: Puzzling Infectious Proteins," 
http://science- 

education.nih.gov/nihHTML/ose/snapshots/multimedia/ritn/prions/prionsl.html , 8 August 
2003. 



1-14 



18 AFMAN 10-2602, Nuclear, Biological, Chemical, and Conventional (NBCC) Defense 
Operations and Standards (Operations), 1 December 2002. 

19 USDA, APHIS, "Protocol for Military Clearance," 18 June 2001. 

20 BG Russ Zajtchuk, et al. (eds.), Textbook of Military Medicine: Medical Aspects of 
Chemical and Biological Warfare, Office of the Surgeon General, 1997, Chapter 21, "The 
Biological Warfare Threat." 

21 TM 3-216/AFM 355-6, Technical Aspects of Biological Defense, 12 January 1971. 

22 BG Russ Zajtchuk, et al. (eds.), Textbook of Military Medicine: Medical Aspects of 
Chemical and Biological Warfare, Office of the Surgeon General, 1997, Chapter 20, "Use of 
Biological Weapons." 

23 FM 8-284/NAVMED P-5042/AFMAN (I) 44-156/Marine Corp Reference Publication 
(MCRP) 4-11. 1C, Treatment of Biological Warfare Agent Casualties, 17 July 2000. 

24 BG Russ Zajtchuk, et al. (eds.), Textbook of Military Medicine: Medical Aspects of 
Chemical and Biological Warfare, Office of the Surgeon General, 1997, Chapter 30, 
"Defense Against Toxin Weapons." 

25 FM 8-9/NAVMED P-5059/AFJMAN 44-151, NATO Handbook on the Medical Aspects of 
NBC Defense Operations AMEDD- 6(B), 1 February 1996. 

26 CDC, NOISH, Documentation for Immediately Dangerous to Life or Health 
Concentrations, National Technical Information Service (NTIS) Publication No. PB-94- 
195047, May 1994. 

27 Mark Davis, Baseline Study on the Problem of Obsolete Pesticide Stocks, Food and 
Agriculture Organization of the United Nations (FAO) Pesticide Disposal Series N.9, 2001. 

28 US EPA, "Pesticides: Health and Safety: Human Health Issues," 19 May 2003, 
http://www.epa.gov/pesticides/health/human.htm , 19 August 2003. 



1-15 



Chapter II 
CHEMICAL WARFARE AGENTS AND THEIR PROPERTIES 

1. Background 

The CW agents can be classified according to their physiological effects or their 
military use; they include choking, nerve, blood, blister, and incapacitating agents. 1 This 
chapter contains definitions for selected physical and chemical properties; definitions for 
selected toxicity terms; and the physical, chemical, and physiological properties of selected 
CW agents and precursors listed in Table II- 1. 

Table 1 1-1. List of Selected CW Agents and Precursors 

2. Definitions of Selected Physical and Chemical Properties 

The definitions for the physical and chemical properties are given in the same order 
listed in the chemical agent tables. 

a. Molecular Weight (MW). MW is the value represented by the sum of the atomic 
weights of all the atoms in a molecule. 2 See Table C-l (page C-l) for the Periodic Table of 
Elements and Table C-2 (page C-2) for the list of elements and their symbols. For example, 
the MW of ethyldichloroarsine (ED), C2H5ASCI2, is computed as follows: 

C (atomic weight = 12.011) x 2 = 24.02 

H (atomic weight = 1.0079) x 5 = 5.04 

As (atomic weight = 74.9216) x 1 = 74.92 

CI (atomic weight = 35.453) x2= 70.91 

MW= 174.89 

b. Physical State. Chemical agents may exist as solids, liquids, or gases. 2 To a 
certain extent the state in which an agent normally exists determines its use, duration of 
effectiveness, and physiological action. It also determines the type of munitions used for its 
dissemination. 

c. Odor. Odor is the emanation from any substance that stimulates the olfactory 
cells in the organ of smell. 3 

d. Boiling Point. The boiling point is the temperature at which the vapor pressure 
of a liquid equals the pressure of the gas above it. The normal boiling point is the 
temperature at which the vapor pressure of a liquid equals one atmosphere (atm). At high 
altitudes where the atmospheric pressure is less than one atm, water boils below 100 
degrees Celsius (C) or 212 degrees Fahrenheit (F). 2 

e. FP/MP. The FP is the temperature at which the solid and liquid phases of a 
given substance are in equilibrium and is generally equivalent to the MP. 2 

NOTE: Some liquids can be cooled well below their freezing temperatures and 
still remain in a liquid state. This extended form of the liquid physical state is 
called "supercooling." Supercooled liquids are unstable and can crystallize 



ll-l 



spontaneously. Constant agitation and/or the use of seed crystals can sometimes 
prevent or reduce the amount of supercooling that occurs. However, many 
chemical agents experience some degree of supercooling, especially the G agents. 
Due to the potential for supercooling, freezing point values should be used with 
caution. Whenever possible, MP valves should be used because they are more 
thermodynamically reproducible than the FP. 4 

f. Density (Liquid/Solid). The density of a chemical agent is the mass per unit 
volume of the substance. Because volume varies with temperature, a specified temperature 
should be given. The density of a liquid or solid is usually given as grams per milliliter 
(g/ml) or grams per cubic centimeter (g/cm 3 ). 2 

NOTE: Solid density can be further specified as bulk (or apparent) density or 
crystalline (or true) density. Both properties describe the mass per unit volume. 
Bulk density includes the volume of the voids, pores, or empty spaces between 
particles, whereas crystalline density includes only the volume occupied by the 
material itself. 5 

g. Vapor Density. Vapor density is the ratio of the weight of a given volume of a 
gaseous substance and that of the same volume of another gas measured under the same 
conditions of pressure and temperature. 6 For the purpose of this manual, the other gas is 
air. To calculate the vapor density, divide the MW of the compound of interest by 29 (the 
average MW of air). If the vapor density is less than 1, the gas will generally rise in the air. 
If the vapor density is greater than 1, the gas will generally settle on the ground. 

h. VP. The VP is the pressure exerted by a vapor when a state of equilibrium exists 
between the vapor and its liquid (or solid) state. It is the pressure in a closed space above a 
substance when no other gas is present. The VP varies with temperature, so the 
temperature should be stated. The VP increases as temperature increases. 2 

i. Volatility. Volatility is the tendency of a solid or liquid material to pass into the 
vapor state at a given temperature. 7 The volatility depends on vapor pressure and varies 
with temperature. Volatility is expressed as milligrams of vapor per cubic meter (mg/m 3 ). 
It is calculated numerically by an equation derived from the perfect gas law: 



V= 16020 xMWxVP 

T 

Where 

V = Volatility (mg/m 3 ) 

MW = molecular weight 

VP = vapor pressure (in torr at a specified temperature) 

T = Kelvin temperature (degrees C + 273.15) 

j. Latent Heat of Vaporization. The latent heat of vaporization is the quantity of 
energy absorbed or given off as a substance undergoes a change in state with no change in 
temperature. 7 It is calculated using the following equation: 8 

AHv = In 10 RBT 2 



(C + 1) 2 



Where 



AHv = Enthalpy of vaporization (latent heat of vaporization) 

T = Kelvin temperature = (degrees C + 273.15) 

R = Ideal gas law constant (1.987 cal K 1 mol 1 ) 

B,C = Vapor pressure constants (from Antoine or Clausius Clapeyron fit) 

t = Temperature in degrees C 

k. Viscosity. Viscosity is resistance that a gaseous or liquid system offers to flow 
when it is subjected to a shear stress. 9 The more complex the molecules in a liquid and the 
stronger the intermolecular forces between them, the more difficult it is for the molecules to 
move past each other and the greater the viscosity of the liquid. A fluid with a large 
viscosity resists motion. Also, as temperatures increase, the viscosity of the liquid 
decreases. 2 Units for viscosity are given in centipoises (cP). 

1. Surface Tension. Surface tension is the force that causes the surface of a liquid 
to contract, reducing its surface area to a minimum. The molecules within a liquid are 
attracted equally in all directions by the cohesive forces within the liquid. However, the 
molecules on the surface of a liquid are attracted only into the liquid and to either side. 
This unbalanced molecular attraction tends to pull the surface molecules back into the 
liquid such that the minimum number of molecules possible are on the surface. 2 Units for 
surface tension are dynes per centimeter (dynes/cm). 

m. Flash Point. The flash point is the temperature at which a liquid or volatile solid 
gives off sufficient vapor to form an ignitable mixture near the surface of the liquid. 7 

n. Decomposition Temperature. The decomposition temperature is the temperature 
at which a chemical breaks down into two or more substances. 4 Because reaction rates 
vary; decomposition temperature is a function of both temperature and time (some 
reactions are slower than others). 



11-3 



o. Solubility. The solubility of a solute is the quantity that will dissolve in a given 
amount of solvent to produce a saturated solution. 2 

p. Hydrolysis. Hydrolysis is the reaction of a compound with water whereby 
decomposition of the substance occurs. 2 New substances (hydrolysis products) form when a 
compound reacts with water. 

q. Half-Life of a Reaction (ti/2). This is the time required for half of the original 
concentration of the limiting reactant to be consumed. 4 

r. Stability in Storage. Stability in storage determines the practical usefulness of a 
compound. If a compound decomposes in storage, it will have little military operational 
value. The addition of stabilizers will typically slow down decomposition and 
polymerization in storage. 

s. Action on Metals, Plastics, Fabrics, and Paint. This item describes the action 
between a given compound and different materials. Depending on their activity, some 
chemicals can react with and degrade materials they contact. Chemical agent-resistant 
coating (CARC) can minimize this effect. 

t. Specific Heat. The specific heat is the quantity of heat required to raise the 
temperature of 1 gram of a substance 1 degree C 2 (given in lieu of latent heat of 
vaporization for military chemical compounds only). 

3. Definitions of Toxicity-Related Terms 

a. ROE. Chemical agents enter the body through the respiratory tract, skin, eyes, 
and by ingestion. Any part of the respiratory tract, from the nose to the lungs, may absorb 
inhaled gases and aerosols. For some agents, effects are more severe in normally sweaty 
areas. The skin can also absorb vapors. The surface of the skin, eyes, and mucous 
membranes can absorb droplets of liquids and solid particles. Wounds or abrasions are 
probably more susceptible to absorption than the intact skin. Chemical agents can 
contaminate food or drink, and therefore, the body can absorb them through the 
gastrointestinal tract. Nerve agents exert their toxic effects through the skin, eyes, and 
lungs. Inhalation is the usual route of exposure for blood agents. Blister agents damage 
skin and other tissues that they contact, to include eyes and lungs. The choking agents 
exert their effects only if inhaled. The onset and severity of signs may vary, depending 
upon the ROE and dosage. 1 The ROEs have been limited to those that are likely to be 
encountered in the field: vapor inhalation with eye exposure, skin exposure to vapor, and 
skin exposure to liquid. The toxicity estimates given for percutaneous vapor exposure for 
the nerve agents are based on bare skin exposures. The toxicity estimates for mustard 
agent percutaneous vapor exposure are based on clothed skin exposures. Effective dosages 
of liquid on the skin are based upon data for bare skin. 9 

b. Dosage. Dosage is the amount of substance administered (or received) per 

body weight. 11 In this manual, dosage is usually expressed as milligrams per kilogram 
(mg/kg) of body weight for liquid agents and as milligrams-minute per meter cubed for (mg- 
min/m 3 ) for vapor exposure. Dosages are given for a 70-kg man. 9 

(1) Median Lethal Dosage (LD50) of Liquid Agent. The LD 50 is the amount of 
liquid agent expected to kill 50 percent of a group of exposed, unprotected individuals. 

(2) Median Effective Dosage (ED50) of Liquid Agent. The ED50 is the amount of 
liquid agent expected to cause some defined effect (e.g., severe, such as prostration, 



collapse, convulsions; mild, such as erythema) in 50 percent of a group of exposed, 
unprotected individuals. 

(3) Median Lethal Dosage (LCtso) of a Vapor or Aerosol. The LCtso of a 
chemical agent in vapor form is the dosage that is lethal to 50 percent of exposed, 
unprotected personnel for a defined MV and exposure duration. 

(4) Median Effective Dosage (ECtso) of a Vapor or Aerosol. The ECtso is the 
effective dosage of a chemical agent vapor that is sufficient to cause some defined effect in 
50 percent of exposed, unprotected personnel for a defined MV and exposure duration. 

NOTES: 

1. Effective dosages can be calculated for more or less than the median dosage 
(e.g., LCt25, ED84). Such calculations require knowledge of the probit (Bliss) slope 
and use the probit equation. 10 

2. Selected toxicity estimates are assigned provisional values. A toxicity estimate 
is considered provisional based on only having limited data, but the data are 
within the range of available animal data or when the agent is presumed to be 
comparable in toxicity to a related agent. 10 

3. Physiological Stressors. Physiological stressors include anxiety, heat, and 
humidity and are likely to reduce toxicity estimates. In other words, the agent is 
potentially more effective. 10 

c. Modifying Factors. After exposure to a chemical agent vapor, a person may show 
signs and symptoms that are less or more severe than expected. The severity of the effects 
may depend upon some of the following potential variables: 

(1) How long the person held his or her breath during short exposure. 

(2) Speed with which he or she donned the mask. 

(3) Proper fit of the mask. 

(4) Whether the body absorbed the agent through the skin. 

(5) Whether the agent increased the MV. 

(6) MV of the person at the time of exposure. 

(7) Physical exertion of the person at the time of exposure. 

(8) Rate of detoxification, especially if exposure was long. 

(9) Previous exposure to chemical agents and type of agent. 

d. MV. The MV is the volume of air exchanged in one minute. In general, as the 
MV increases, the apparent dosage decreases because more agent is inhaled into the lungs. 
It is important to note that increasing respiratory rate does not necessarily increase MV 
and may actually decrease it. The relationship of MV to dosage is approximately linear 
over ranges of MV from 10 to 50 liters. For example, if the LCtso is given as 35 mg-min/m 3 , 
for an MV of 15 liters, it would be approximately 50 mg-min/m 3 for an MV of 10 liters and 
approximately 15 mg-min/m 3 for an MV of 30 liters. 3 Where available, MV profile tables 
are provided in Appendix H. 



11-5 



e. Exposure Duration. The official interim standards for inhalation/ocular 
exposures are for a 2-minute duration; those for percutaneous vapor exposure (masked 
personnel) are for a 30-minute duration. More data have become available since the 
interim standards were defined, and they are also given for longer exposures, as data are 
available. 10 

f. Temperature. Selected agents have toxicity estimates for hot and moderate 
temperatures. Hot temperatures are defined as greater than 85 degrees F. Moderate 
temperatures are defined as 65 to 85 degrees F. In general, as the temperature increases, 
the effective dosage decreases. The dosages for hot temperatures are about half of those for 
moderate temperatures. 10 

g. Endpoint (Physiological Effects). Toxicity estimates are provided for different 
endpoints to include lethality, severe effects, threshold effects, and mild effects. 

(1) For nerve agents, severe effects include prostration, collapse, and/or 
convulsions. Some deaths will occur. Threshold effects for percutaneous vapor exposure 
include slight, not necessarily significant, ChE inhibition and/or localized sweating. Mild 
effects following inhalation/ocular exposure include miosis, rhinorrhea, and tight chest. 
These effects can occur in the absence of measurable ChE inhibition in the blood. 10 

(2) For percutaneous exposure to blister agents, severe effects include 
vesication and mild effects include erythema, edema, pain, and itching — depending upon 
the agent. Severe effects following ocular exposure include pain, conjunctivitis, 
blepharospasm, and temporary blindness; mild effects consist of erythema and minimal 
conjunctivitis. 10 

h. ROD. The human body can detoxify some toxic materials. The ROD is an 
important factor in determining the hazards of repeated exposure to CW agents. Many CW 
agents are essentially cumulative in their effects. 

i. ROA. The ROA of a chemical agent is the rate at which the body reacts to or is 
affected by that agent. The rate varies widely, even between those of similar tactical or 
physiological classification. 

j. Concentration-Time (Ct) Profile. Dosage is a function of Ct; however, the 
equation k=Ct does not describe all cases of injury from chemical agent exposure. As seen 
in some Ct profile tables, a given effective dosage does not always produce a specific effect 
for all duration exposures. In order to describe the effective dosages better mathematically, 
the equation C n t=k is used. The exponent "n" is called the toxic load exponent (TLE). See 
Figure II- 1 and II-2 (page II- 8) 

(a) When the TLE value is greater than 1, effective dosages increase as the 
exposure duration increases (and the exposure concentration decreases). 

(b) When the TLE value is less than 1, effective dosages decrease as the 
exposure duration increases (the agent is more potent following long exposures to low 
concentrations than short exposures to high concentrations). 

(c) When the TLE value equals 1 (Haber's Law), a given dosage (Ct) produces a 
given effect — independent of concentration or exposure duration. When the Ct profile is 
unknown, a default exponent value of one is used (TLE is assumed to be 1). 



11-6 



The effect the TLE has on the effective dosage is illustrated in the following Ct profile tables. In the 
equation k-C n t, there are three possible cases for the value of the TLE(n). 

Case1:TLE>1 

NOTES: 

• LCt 5 o/ECt 5 o increases as exposure 
duration increases. 

• Concentration decreases; exposure to 
low levels for an extended period of time 
can cause effects. 

• There is no single LCt/ECt for a specific 
type of exposure and endpoint. 



Ct Profile (15LMV) 


Exposure 
Duration (min) 


LCtso 
(mg-min/m 3 ) 


Concentration 
(mg/m 3 ) 


2 


35 


17.5 


60 


70 


1.2 


120 


80 


0.7 



Ct Profile (15LMV) 


Exposure 
Duration (min) 


LCt 50 
(mg-min/m 3 ) 


Concentration 
(mg/m 3 ) 


2 


35 


17.5 


60 


20 


0.3 


120 


15 


0.125 



Case 2: TLE<1 

NOTES: 



LCt 50 /ECt 5 o decreases as exposure 
duration increases. 

The agent is more potent following long 
exposures to low concentrations than 
short exposures to high concentrations. 
There is no single LCt/ECt for a specific 
type of exposure and endpoint. 



Case 3: TLE =1 {H aber's Law) 
NOTES: 



Ct Profile (15LMV) 


Exposure 
Duration (min) 


LCtso 
(mg-min/m 3 ) 


Concentration 
(mg/m 3 ) 


2 


35 


17.5 


60 


35 


0.5 


120 


35 


0.3 



LCt 50 /ECt 5 o remains constant as 
exposure duration increases. 
Concentration decreases; exposure to 
low levels for an extended period of time 
can cause effects. 

There is a single LCt/ECt for a specific 
tvDe of exposure and endDoint. 



Figure ll-l. The TLE Effect on the Ct Profile 



II-7 



Dosage vs. Exposure Duration 



O 



Case 1 



Case 2 



Case 3 



Time (minutes) 
Example TLE > 1 (Case 1) 

CW Agent Vapor: Dosage versus Exposure Duration 

10 



E 



O 



0.0 




The graph on the left is a representation of a Ct 
profile for dosage versus exposure duration. The 
graph is constructed by plotting the exposure 
duration (t) on the horizontal axis and the dosage 
(k) on the vertical axis. In the quotation k=C n t there 
are three possible cases for the value of the TLE 
(n). The graph shows the three cases. 

Case 1 : TLE > 1 ; LCt50/ECt50 increases as 

exposure duration increases. 
Case 2: TLE < 1; LCt50/ECt50 decreases as 

exposure duration increases. 
Case 3: TLE = 1; LCt50/ECt50 remains constant as 

exposure duration increases. 



This is an example of the Ct profile graphs for 
dosage versus exposure duration given in 
Appendix H. this is for an inhalation/ocular 
vapor exposure to a CW agent. 

Given: 



Upper Band: LCt 16 and LCt 84 region 
Line: ECt 16 (severe) [roughly LCt i] 
Lower Band: ECt 16 and ECt 84 region for mild 
effects 



10 



100 



Time (minutes) 



Upper Band : The endpoint is lethality. The region shows the effective dosages that would be lethal to 16-84% of 70- 
kg males exposed. 

Line : The endpoint is severe effects (specific symptoms depend on the type of CW agent exposure). The line gives 
the effective dosages where 16 percent of 70-kg males would experience severe effects. This is roughly equivalent to 
the lethal dosage for 1 percent. Severe effects can include some deaths. 

Lower Band : The endpoint is mild effects (specific symptoms depend on the type of CW agent exposure). The region 
shows the effective dosages that would cause mild effects in 16-84% of 70-kg males exposed. 

Notice as exposure duration (time) increases, the effective dosage (LCt/ECt) increases. There is no single LCt or ECt 
for an exposure; they are time-dependent. 



Figure 11-2. Ct Profile for Dosage versus Exposure Duration 



11-8 



k. Probit Slope. Dose response curves can be used to assess from a graphical 

depiction the results of an exposure to a CW agent. The dose response curve is impacted by 
the concentration of the CW agent and duration of the exposure (i.e., a graphical x-axis 
plot) and response (i.e., a graphical y-axis plot). The probit slope is derived from dose 
response curve data and corresponds to the variability in the response of the population to 
the chemical agent. 

(a) A high probit slope value means that a small change in the dose will make 
a large change in the number of individuals responding to the chemical agent. With very 
potent agents, a small change in the dose can also make a big change in the level and 
severity of the effects produced. 

(b) A low probit slope value means that a relatively large change in the dose 
will make for a relatively minor change in the number of individuals responding to the 
given dose. 

1. Degree of Confidence (DOC). 10 The DOC is an indication of the level of 
confidence in each toxicity estimate and is provided to indicate uncertainty. It is a 
subjective evaluation based on the quality and quantity of the underlying data and the 
method(s) by which the estimate was derived. The following definitions are provided: 

(1) Low. There are no primary data, and/or the data are extremely limited. 

(2) Moderate. There are primary data for both humans and animals, and there 
are sufficient data for mathematical modeling. 

(3) High. There are ample primary data for both humans and animals, and 
there is good statistical confidence in the value. 

4. Choking Agents 

Choking agents are CW agents that attack lung tissue, primarily causing pulmonary 
edema. They cause irritation to the bronchi, trachea, larynx, pharynx, and nose. Initial 
symptoms may include tears, dry throat, coughing, choking, tightness of chest, nausea, 
vomiting, and headache. 1 In extreme cases, membranes swell, lungs become filled with 
liquid, and death results from lack of oxygen; thus, these agents "choke" an unprotected 
person. Fatalities of this type are called "dry-land drownings." Of the choking agents, 
phosgene (CG) is the only one considered likely to be used in the future. 12 The protective 
mask gives protection against choking agents. 1 

a. CG (see Table II-2 [page 11-10]). CG is a colorless gas with an odor similar to 
musty hay or rotting fruit. 13 Vapors can linger for some time in trenches and low-lying 
areas under calm or light winds. 12 The severity of poisoning cannot be estimated from the 
immediate symptoms, and the full effect can be delayed up to 72 hours after exposure. 14 
Any activity or stress after exposure is likely to exacerbate the effects and turn a sublethal 
exposure into a lethal exposure. 10 Lung damaging concentrations may not be detected by 
smell. 10 



11-9 



Table 11-2. CG 



Alternate Designations: Collongite (French); Zusatz (German); Green Cross (German); D-gas (German); Fosgeen (Dutch); 
Fosgen (Polish); Fosgene (Italian); Phosgen (German); NCI-C60219 


Chemical Name: Carbonyl chloride 


Synonyms: Carbon oxychloride; Carbon dichloride oxide; Carbone (oxychlorure de) (French); Carbonic chloride; Carbonio 
(ossiclorurodi) (Italian); Carbonylchlorid (German); Carbonyl dichloride; Chloroformy chloride; Koolstofoxychloride (Dutch) 


CAS Registry Number: 75-44-5 


RTECS Number: SY5600000 


Physical and Chemical Properties 


Structural Formula: 

P 

o=c 

\ 

CI 

Molecular Formula: COCb 
Molecular Weight: 98.92 


Physical State 


Colorless gas that is readily liquefied 1 


Odor 


Musty hay or rotting fruit 2 


Boiling Point 


7.8°C 3 ' 4 


FP/MP 


-128°C(MP) 5 


Liquid Density (g/mL) 


Liquefied phosgene 1.360 @ 25°C; 1.402 @ 7.8°C; 1.420 @ 0°C 6 


Vapor Density (relative to air) 


3.4 (calculated) 


Vapor Pressure (torr) 


1.40 x 10 3 @ 25°C; 7.60 x 10 2 @ 7.8°C; 5.60 x 10 2 @ 0°C 3 ' 4 


Volatility (mg/m 3 ) 


7.46 x 10 6 @ 25°C; 4.29 x 10 6 @ 7.8°C; 3.53 x 10 6 @ 0°C (calculated from vapor 
pressure) 3| 


Latent Heat of Vaporization 
(kcal/mol) 


5.92 @ 25 C C; 5.95 @ 7.8 C C; 5.96 @ C C (calculated from vapor pressure) 3 ' 4 


Viscosity (cP) 


Data not available 


Viscosity of Vapor (cP) 


Data not available 


Surface Tension (dynes/cm) 


Data not available 


Flash Point 


Nonflammable 1 


Decomposition Temperature 


Complete @ 800°C 7 


Solubility 


Limited in water; 8 miscible with common organic solvents, petroleum, and lubricating oil 

9,10 


Rate of Hydrolysis 


ti/2 = 0.25 sec. @ 13 C C; does not react quickly with water vapor, but it immediately 
reacts with liquid water to yield carbon dioxide and hydrochloric acid 8 ' 11 


Hydrolysis Products 


Hydrochloric acid and carbon dioxide 9 


Stability in Storage 


Stable in steel containers @ ambient temperatures for at least one year if CG is dry; 
stability decreases at elevated temperatures 12 


Action on Metals or Other Materials 


None when CG is dry; acidic and corrosive when moist 13 


Other Data 


Eye toxicity 


Initial effects resemble those of tear gas. 14 


Inhalation toxicity 


Causes pulmonary edema 15 


Rate of action 


Immediate to 3 hours, depending on concentration 16 


Means of detection in field 


M18A2CADK, MM1 17 


Protection required 


Protective mask 15 


Decontamination 


Not required in the field except in very cold climates 


Use 


Delayed action casualty agent 19 



II-10 



Table 11-2. CG (Continued) 



NOTES 



^Matheson Gas Data Book, 4 ed., p. 411, The Matheson Company, Inc., East Rutherford, NJ, 1966. 

2 Franke, S., Manual of Military Chemistry Volume l-Chemistry of Chemical Warfare Agents, ACSI-J-3890, Chemie der 

Kampfstoffe, East Berlin, April 1968, UNCLASSIFIED Technical Manual (AD849866). 

3 Abercrombie, P., ECBC Notebook # NB 98-0079, p. 7 (U). 

4 Germann, A.F.O. and Taylor, Q.W., "The Critical Constants and Vapor Tension of Phosgene," J. Amer. Chem. Soc, Vol. 48(5), 

pp. 1154-1159, 1928. 

5 Giauque, W. F., and Jones, W.M., "Carbonyl Chloride. Entropy. Heat Capacity. Vapor Pressure. Heats of Fusion and 

Vaporization. Comments on Solid Sulfur Dioxide Structures," J. Amer. Chem. Soc, Vol. 70, p. 120, 1948. 

6 Davies, C. N., "The Density and Thermal Expansion of Liquid Phosgene," J. Chem. Phys., Vol. 14, p. 48, 1946. 

7 Bodenstein, M., and Durant, G., "Die Dissociation des Kohlenoxychlorids," Z. Physik. Chem., Vol. 61, p. 437, 1908. 

8 Hall, R.W., An Investigation on the Solubility and Rate of Hydrolysis of Phosgene in Water, Porton Report 2663, Chemical 

Defence Experimental Establishment, Porton, England, 19 December 1944, UNCLASSIFIED Report. 

9 Atkinson, R.H., et al., "The Preparation and Physical Properties of Carbonyl Chloride," J. Chem. Soc, Vol. 117, pp. 1410-1426, 

1920. 

10 Baskerville, C, and Cohen, P.W., "Solvents for Phosgene," J. Ind. Eng. Chem., Vol. 13, p. 333, 1921. 

^Properties of War Gases Volume III: Vomiting & Choking Gases & Lacrimators (U), ETF 1 00-41 A/ol-3, Chemical Corps Board, 

Army Chemical Center, MD, December 1944, CONFIDENTIAL Report (AD1 08458). 

12 Henley, F.M., Surveillance Tests on 75 MM. Steel Gas Shell Extending Over a Period of One Year, EACD 1 1 , Chemical 

Warfare Service, Edgewood Arsenal, MD, June 1920, UNCLASSIFIED Report (ADB959731). 

13 Patten, H.E., and Bouder, N.M., Chemical Properties of Phosgene, EACD 124, Chemical Warfare Service, Edgewood 

Arsenal, MD, March 1923, UNCLASSIFIED Report (ADB955133). 

14 BG Russ Zajtchuk, et al. (eds.), Textbook of Military Medicine: Medical Aspects of Chemical and Biological Warfare, Office of 

the Surgeon General, 1997, Chapter 4, The Chemical Warfare Threat and the Military Healthcare Provider." 

15 FM 8-285/NAVMED P-5041/AFJMAN 44-149/FMFM 11-11, Treatment of Chemical Agent Casualties and Conventional 

Military Chemical Injuries, 22 December 1995. 

1B NIOSH-DOD-OSHA Sponsored Chemical and Biological Respiratory Protection Workshop Report, February 2000. 

17 AFMAN 10-2602 Nuclear, Biological, Chemical, and Conventional (NBCC) Defense Operations and Standards (Operations), 

29 May 2003. 

18 FM 8-9/NAVMED P-5059/AFJMAN 44-151, NATO Handbook on the Medical Aspects of NBC Defense Operations AMEDP- 

6(B), 1 February 1996. 

19 W.R. Kirner, Summary Technical Report of Division 9, NDRC Volume 1, Chemical Warfare Agents, and Related Chemical 

Problems Part /-//, Office of Scientific Research and Development, Washington, DC, 1946, UNCLASSIFIED Report 

(AD234270). 



b. CG Toxicity Estimates (see Table II-3). Although the probit slope for CG is 
unknown, it is known to be so steep that "incapacitating" or "severe effects" dosages could 
include some lethality. 10 

Table 11-3. CG Toxicity Estimates 10 



Endpoint 


Toxicity 
(mg-min/m 3 ) 


MV(L) 


Exposure 
Duration 


ROE 


Probit 
Slope 


TLE 


ROD 


DOC 


Lethality 


LCt 50 : 1500 a 


15 


2-60 min 


Inhalation/Ocular 


Unknown 


1 b 


Probably 
Insignificant 


Moderate 


Odor 
Detection 


EC 50 : 6 mg/m 3c 


N/A 


Few 
Seconds 


Inhalation 


N/A 


N/A 


Probably 
Insignificant 


Low 


NOTES 


a Based on ECBC modeling of 10 mammalian species. 
b See Appendix H for supporting toxicity profile estimates. 
c Based on secondary human data and TM 3-215 (1952). 



c. Diphosgene (DP) (see Table II-4 [page 11-12]). DP is a colorless liquid with an 
odor similar to that of musty hay. 13 DP is not a polymer of CG, but does produce similar 
physiological effects. DP is described as a respiratory irritant and a lachrymator. It is 
more easily detected than CG because of its lacrimatory effects. 9 See Table II-5 (page II- 
13) for DP toxicity estimates. 



11-11 



Table 11-4. DP 



Alternate Designations: Difosgene; Superpalite (British); Perstoff (German); Surpalite(French); Green Cross (German) 


Chemical Name: Trichloromethyl chloroformate 


Synonyms: Trichloromethyl chlorocarbonic acid ester; Chloroformic acid trichloromethyl ester; Trichloromethyl 
chlorocarbonate; Trichloromethyl carbonochloridate; Formic acid, chloro-, trichloromethyl ester; Carboncohloridic acid 
trichloromethyl ester 


CAS Registry Number: 503-38-8 


RTECS Number: LQ7350000 


Physical and Chemical Properties 


Structural Formula: 



II CI 
/C\ 1 

cr o— c— ci 

I 

CI 

Molecular Formula: C2CI4O2 
Molecular Weight: 197.83 


Physical State 


Colorless oily liquid 1 


Odor 


Musty hay 2 


Boiling Point 


127°C 3 ' 4 


FP/MP 


-57°C (MP) 2 


Liquid Density (g/mL) 


Munitions grade: 1 .656 @ 20°C; 1 .687 @ 0°C 2 


Vapor Density (relative to air) 


6.8 (calculated) 


Vapor Pressure (torr) 


4.41 @ 20°C; 9.14 x 10" 1 @ 0°C 3 ' 4 


Volatility (mg/mL) 


4.77 x 10 4 @ 20°C; 1.06 x 10 4 @ 0°C (calculated from vapor pressure) 3 ' 4 


Latent Heat of Vaporization (kcal/mol) 


12.2 @ 20°C; 12.8 @ C C (calculated from vapor pressure) 3 ' 4 


Viscosity (cP) 


Data not available 


Viscosity of Vapor (cP) 


Data not available 


Surface Tension (dynes/cm) 


Data not available 


Flash Point 


None 5 


Decomposition Temperature 


300°C to 350°C (yields two molecules of CG) 1 


Solubility 


Solubility in water is 44.6 g DP/L solution @ 20°C; 6 readily soluble in common 
organic solvents 2 


Rate of Hydrolysis 


Slow @ ambient temperature and fairly rapid @ 100°C 1 


Hydrolysis Products 


Hydrogen chloride (HCI) and carbon dioxide 1 


Stability in Storage 


Unstable; converts to CG. 1 


Action on Metals or Other Materials 


Metals act as catalyzers in conversion to CG. 1 ' 2 Also attacks rubber, cork, 2 ' 4 and 
cement. 2 


Other Data 


Eye toxicity 


Lachrymator 7 


Inhalation toxicity 


Causes pulmonary edema 


Rate of action 


Immediate to 3 hours depending on concentration 9 


Means of detection 


MM1 


Protection required 


Protective mask 


Decontamination 


Not required in the field except in very cold climates. 10 


Use 


Delayed or immediate action casualty agent, depending on dosage rate 



-12 



Table 11-4. DP (Continued) 



NOTES 



'Hood, H.P., and Murdock, H.R., "Superpalite," J. Phys. Chem., Vol. 23, p. 498, 1919. 

2 Potts, A.M., The Physical and Chemical Properties of Phosgene and Diphosgene, OEMCMR-1 14, 1945, UNCLASSIFIED 

Report. 

3 Abercrombie, P., ECBC Notebook* NB 98-0079, p. 34 (U). 

4 Herbst, V.H., "Uber die Fluchtigkeit und Vernebelung einer Reihe organischer Stoffe," Kolloid Beihefte, Vol. 23, p. 330, 

1927. 

5 TM 3-215/AFM 355-7, Military Chemistry and Chemical Agents, December 1963, UNCLASSIFIED Technical Manual. 

6 Carter, R.H., and Knight, H.C., Fundamental Study of Toxicity Solubilities of Certain Toxics in Water and in Olive Oil, EACD 

445, Chemical Warfare Service, Edgewood Arsenal, Edgewood, MD, May 1928, UNCLASSIFIED Report (ADB955216). 

7 Sharon Reutter, et al., Review and Recommendations for Human Toxicity Estimates for FM 3-11.9, ECBC-TR-349, 

September 2003. 

8 FM 8-285/NAVMED P-5041/AFJMAN 44-149/FMFM 11-11, Treatment of Chemical Agent Casualties and Conventional 

Military Chemical Injuries, 22 December 1995. 

9 NIOSH-DOD-OSHA Sponsored Chemical and Biological Respiratory Protection Workshop Report, February 2000. 

10 FM 8-9/NAVMED P-5059/AFJMAN 44-151, NATO Handbook on the Medical Aspects of NBC Defense Operations 

AMEDP-6(B), 1 February 1996. 



Table II-5. DP Toxicity Estimates 



10 



Endpoint 


Toxicity 
(mg-min/m 3 ) 


MV(L) 


Exposure 
Duration 


ROE 


Probit 
Slope 


TLE 


OD 


DOC 


Lethality 


LCt 50 : 1500 a 
(Provisional) 


15 


10-60 min 


Inhalation/ 
Ocular 


Unknown 


a b,c 


Unknown, 

Probably 

Insignificant 


Low 


Odor 
Detection 


EC 50 : 4mg/m 3d 


N/A 


Few 
Seconds 


Inhalation 


N/A 


N/A 


N/A 


Low 


NOTES 


a Based on recommendations for CG. 

b The TLE value is assumed to be 1 because the Ct profile is unknown. 

c See Appendix H for supporting toxicity profile estimates. 

d Based on secondary human data. 



5. Nerve Agents 

Nerve agents are more toxic than other CW agents. They may cause effects within 
seconds and death within minutes. 15 The nerve agents are all liquids, not nerve gas per se. 
They can be absorbed through any body surface and can penetrate ordinary clothing 
rapidly. 1 They are divided into the G agents and V agents. The V agents have high boiling 
points, low volatility, and resultant high persistency. 12 Even though the V agents are 
considered primarily a contact hazard 12 ; they are at least twice as potent as GB, and even a 
minute amount of airborne material is extremely hazardous. 10 Nerve agents are 
cumulative poisons. Repeated exposure to low concentrations may produce symptoms. 1 
Level 4 mission-oriented protective posture (MOPP4) is required for protection. 1 

a. Physiological Effect. Both the G and V agents have the same physiological 
action on humans. Normally, the enzyme acetylcholinesterase (AChE) binds and 
hydrolyzes the neurotransmitter ACh, which terminates the activity of ACh at the receptor 
sites. Upon exposure, the nerve agents bind to AChE, making it unable to bind with ACh. 
As a result, ACh is not hydrolyzed. The accumulation of ACh causes hyperactivity of the 
body organs stimulated by cholineraic neruons. 15 Individuals poisoned by nerve agents 
may experience symptoms in the following order: 

• Miosis, runny nose, and chest tightness. 

• Dim vision and headache. 

• Nausea, vomiting, and cramps. 



11-13 



• Drooling, excessive sweating, drowsiness, and confusion. 

• Difficulty breathing, twitching, jerking, and staggering. 

• Convulsions and coma. 

b. Miosis. When airborne vapor comes in contact with the eyes, miosis occurs as a 
result of a direct local effect of the nerve agent on the eyes and can occur prior to any 
inhibition of ChE in the blood. This type of exposure is frequently accompanied by 
tightness of the chest and/or rhinorrhea, and any or all other symptoms can occur. In cases 
of nerve agent exposure not involving vapor contact with the eyes, miosis is one of the last 
effects to occur before death. 10 

c. Treatment. Treatment of nerve agent poisoning includes use of atropine, 2-PAM 
chloride, convulsant antidote for nerve agents (CANA), and pyridostigmine bromide (PB). 

(1) Atropine binds to receptor sites blocking the excess acetylcholine caused by 
nerve agent poisoning. 

(2) 2-PAM CI acts by reactivating ChE inhibited by a nerve agent. 15 Prompt 
treatment is essential because after the agent binds to AChE, a second reaction occurs in 
which the agent loses one alkyl or alkoxy group. This phosphorylated AChE is called an 
"aged" enzyme and is completely resistant to both spontaneous and oxime-medicated (2- 
PAM CI) reactivation. The "aging" period varies from minutes to hours depending on the 
type of agent. 16 For GD, the "aging" half-time is within 2 minutes. 17 

(3) The CANA prevents and treats convulsions caused by exposure to nerve 
agents in moderate to severe cases. 1 

(4) PB is a pretreatment for exposure to GD. PB and AChE bind and form 
what is called a carbamoylated AChE. Although PB is also an AChE inhibitor, it is unlike 
nerve agents in that the interaction between PB and AChE is freely and spontaneously 
reversible and it does not undergo the aging process. The carbamoylated AChE is fully 
protected from attack by nerve agents. Atropine is still needed to counteract the excess 
ACh and 2-PAM CI is still needed to reactivate AChE active sites that were protected by 
PB. 17 PB is available to US forces in active theaters of operation (TOs). 1 

d. Tabun (GA) (see Table II-6). GA was the first of the nerve agents developed by 
the Germans. 15 GA is primarily an inhalation hazard. See Table II-7 (page 11-17) for GA 
toxicity estimates. 

Table 11-6. GA 

Alternate Designations: EA 1205; Le-100 (German), T-83 (German); MCE; FM-511; T-2104 (British); TL-1578 (UCTL); 

Trilon 83 (German); Gelan I (German); Taboon A 

Chemical Name: Ethyl N, N-dimethylphosphoroamidocyanidate 

Synonyms: Ethyl dimethylamidocyanophosphate; Dimethylaminoethoxyphosphoryl cyanide; 

Dimethylaminocyanophosphoric acid ethyl ester; Cyanodimethylaminoethoxyphosphine; 

Dmethylaminecyanoethoxyphosphine oxide; Ethyl dimethylaminocyanophosphonate Phosphoramidocyanidic acid, dimethyl, 

ethyl ester; Dimethylamidoethoxyphosphoryl cyanide; Dimethylaminocyanphosphorsaeureaethylester (German); 

Dimethylphosphoramidocyanidic acid, ethyl ester; Ethyl dimethylphosphoramidocyanidate; Ethylester-dimethylamid kyseliny 

kyanfosfonove (Czech) 

CAS Registry Number: 77-81-6 
RTECS Number: TB4550000 



II-14 



Table 11-6. GA (Continued) 



Physical and Chemical Properties 


Structural Formula: 

II / CH 3 

CH 3 CH 2 — 0— P— N 

CN CH 3 

Molecular Formula: C5H11N2O2P 
Molecular Weight: 162.13 


Physical State 


Colorless to brown liquid 1 


Odor 


Faintly fruity; none when pure 2 


Boiling Point 


248°C (extrapolated) 3 " 7 


FP/MP 


-50°C (FP) 5 


Liquid Density (g/mL) 


1 .0756 @ 25°C; 1 .0999 @ 0°C 3 


Vapor Density (relative to air) 


5.6 (calculated) 


Vapor Pressure (torr) 


5.70 x 10" 2 @ 25°C; 4.75 x 10" 3 @ 0°C (extrapolated) 3 " 7 


Volatility (mg/m 3 ) 


4.97 x 10 2 @ 25°C; 4.52 x 10 1 @ C C (calculated from vapor pressure) 3 " 7 


Latent Heat of Vaporization (kcal/mol) 


15.5 @ 25°C; 16.7 @ C C (calculated from vapor pressure) 3 " 7 


Viscosity (cP) 


[email protected]°C, 4.320@ 0°C 3 


Viscosity of Vapor (cP) 


6.20 x 10' 3 @ 25.0°C, 5.60 x 10" 3 @ 0°C 3 


Surface Tension (dynes/cm) 


32.5 @ 25.0°C, 35.0 @ 0°C 3 


Flash Point 


78°C (closed cup) 8 


Decomposition Temperature 


Decomposes completely @ 150°C after about 3 to 3 1/4 hrs 9 


Solubility 


Solubility in water is approximately 7.2g GA/100g solution @ 20°C and 9.8g 
GA/100g @ 0°C; 3 readily soluble in common organic solvents 2 


Rate of Hydrolysis 


ti/2 = 8.5 hrs @ 20°C and pH 7; 10 slow in water but fairly rapid with strong acids and 
alkalis with self-buffering @ pH 4 to 5; 1 autocatalytic below pH 4 11 


Hydrolysis Products 


AC, dimethylaminocyanophosphonic acid, and other products 10 


Stability in Storage 


When stabilized with 5% chlorobenzene, GA can be stored in steel containers for 
several years @ ambient temperatures. The degree of stability decreases @ 
elevated temperatures with decomposition occurring within 6 months @ 50°C and 
3 months @ 65°C. 12 


Action on Metals or Other Materials 


Corrosion rate of steel on crude GA with 5 to 20% chlorobenzene is 0.000034 
inch/month @ 65°C. 12 


Other Data 


Skin and eye toxicity 


Eyes: very high; much greater through eyes than through skin. Skin: highly toxic, 
decontamination of smallest drop of liquid agent is essential; liquid penetrates skin. 

13 


Inhalation Toxicity 


Primarily inhalation hazard 14 


Rate of action 


Rapid 15 


Means of detection 


M8 paper, M9 paper, M256A1 CADK, M8A1 ACAA, M90 AMAD, M21 ACAA, M22 
ACADA, CAM/ICAM, M272 Water Testing Kit, M18A3 CADK 16 , M18A2 CADK, 
MM1, CAPDS, IPDS, AN/KAS-1 CWDD 16 


Protection required 


MOPP4; liquid nerve agents penetrate ordinary clothing rapidly 13 


Decontamination 


Flush eyes with water immediately. Use the M291 SDK to remove any liquid nerve 
agent on skin or clothing. Use the M295 IEDK for individual equipment. 13 STB is 
effective on equipment. Water, steam, and absorbents (earth, sawdust, ashes, 
and rags) are effective for physical removal. 17 NOTE: GA may react to form CK 
in bleach slurry. 18 


Use 


Quick-acting casualty agent 



11-15 



Table 11-6. GA (Continued) 



NOTES 



1 Witten, Benjamin, The Hydrolysis of MCE, Technical Division Memorandum Report 1121, USA Chemical Research and 

Development Laboratories, Army Chemical Center, MD, August 1945, UNCLASSIFIED Report (ADB964102). 

2 Welchman, R.M.A., Preliminary Report on the Potential Value of Nerve Gases as C.W. Agents, Porton Report No. 2747 

(PR 2747), Chemical Defence Experimental Establishment, Porton, England, January 1947, UNCLASSIFIED Report. 

3 Samuel, J.B., et al., Physical Properties of Standard Agents, Candidate Agents, and Related Compounds at Several 

Temperatures (U), ARCSL-SP-83015, USA Armament Research and Development Command, Aberdeen Proving Ground, 

MD, June 1983, UNCLASSIFIED Report (ADC033491). 

4 Abercrombie, P., ECBC Notebook # NB 98-0079, p. 36 (U). 

5 Harris, B.L., Physical Constants of MCE, Technical Division Memorandum Report 1094, USA Chemical Research and 

Development Laboratories, Army Chemical Center, MD, July 1945, UNCLASSIFIED Report (ADB 964103). 

6 Balson, E.W., Determination of the Vapor Pressure of T 2104, A.3804/3, Military Intelligence Division, Chemical Defence 

Experimental Establishment, Porton, England, April 1945, UNCLASSIFIED Report. 

7 Belkin, F., and Brown, H.A., Vapor Pressure Measurements of Some Chemical Agents Using Differential Thermal Analysis, 

Part III, ECTR-75032, Edgewood Arsenal, Aberdeen Proving Ground, MD, June 1975, UNCLASSIFIED Report 

(ADA010666). 

8 Walpole, J.L., Determination of the Flash Points of GA and GB, Porton Technical Paper No. 45 (PTP 45), Chemical 

Defence Experimental Establishment, Porton, England, March 1948, UNCLASSIFIED Report. 

9 Miller, C.E., Thermal Studies on MCE, Technical Division Memorandum Report 1132, USA Chemical Research and 

Development Laboratories, Army Chemical Center, MD, September 1945, UNCLASSIFIED Report (ADB964104). 

10 Marsh, D.J. et al., Kinetics of the Hydrolysis of Ethyl Dimethylamino Cyanophosphonate (and certain other related 

compounds) in Water, Proton Technical Paper No. 85 (PTP-85), Chemical Defense Experimental Establishment, Porton, 

England, December 1948, UNCLASSIFIED Report. 

"Clark, D.N, Review of Reactions of Chemical Agents in Water, Final Report to USA Biomedical Research and 

Development Laboratory, Battelle, Columbus, OH, January 1989, UNCLASSIFIED Report (ADA2 13287). 

12 Harris, B.L. and Macy, R., Storage Stability of German GA in Uncoated and Lacquered 75mm Shell at 50"C and 65"C. 

Corrosion Rate of Steel by GA at 65°C, Technical Division Memorandum Report 1299, USA Chemical Research and 

Development Laboratories, Army Chemical Center, MD, December 1946, UNCLASSIFIED Report (ADB964902). 

13 FM 8-285/NAVMED P-5041/AFJMAN 44-149/FMFM 11-11, Treatment of Chemical Agent Casualties and Conventional 

Military Chemical Injuries, 22 December 1995. 

14 Sharon Reutter, et al., Review and Recommendations for Human Toxicity Estimates for FM 3-11.9, ECBC-TR-349, 

September 2003. 

^NIOSH-DOD-OSHA Sponsored Chemical and Biological Respiratory Protection Workshop Report, February 2000. 

16 DOD Chemical And Biological Defense Program Annual Report to Congress, Volume I, April 2003. 

17 FM 3-5/MCWP 3-37.3, NBC Decontamination, 28 July 2000. 

18 W.R. Kirner, Summary Technical Report of Division 9, NDRC Volume 1, Chemical Warfare Agents, and Related Chemical 

Problems Part /-//, Office of Scientific Research and Development, Washington, DC, 1946, UNCLASSIFIED Report 

(AD234270). 



II-16 







Table II-7. GA Toxicity Estimates 


• 








Endpoint 


Toxicity 
(mg-min/m 3 ) 


MV(L) 


Exposure 
Duration 


ROE 


Probit 
Slope 


TLE 


ROD 


DOC 


Lethality 


LD 50 : 1500 mg a 


N/A 


N/A; 
70-kg man 


Percutaneous 
Liquid b 


5 


N/A 


Unknown 


Low 


LCt 50 : 70 a 


15 


2 min 


Inhalation/Ocular 


12 


1.5 C 


Some 


Moderate 


LCt 50 : 15,000 ad 


N/A 


30-360 min 


Percutaneous 
Vapor e 


5 


1 c < f 


Unknown 


Low 


LCt 50 : 7500 9 ' h 
(Provisional) 


N/A 


30-360 min 


Percutaneous 
Vapor 6 


5 


1 c < f 


Unknown 


Low 


Severe effects, 
includes deaths 


ED 50 : 900 mg a 


N/A 


N/A; 
70-kg man 


Percutaneous 
Liquid b 


5 


N/A 


Unknown 


Low 


ECt 50 : 50 a 


15 


2 min 


Inhalation/Ocular 


10 


1.5 C 


Some 


Moderate 


ECt 50 :12,000 ad 


N/A 


30-360 min 


Percutaneous 
Vapor 6 


5 


1 c < f 


Unknown 


Low 


ECt 50 : 6000 gh 
(Provisional) 


N/A 


30-360 min 


Percutaneous 
Vapor 6 


5 


1 c < f 


Unknown 


Low 


Threshold 
effects (slight 
ChE inhibition) 


ECt 50 : 2000 ad 


N/A 


30-360 min 


Percutaneous 
Vapor 6 


5 


1 c < f 


Unknown 


Moderate 


ECt 50 : 1000 g ' h 
(Provisional) 


N/A 


30-360 min 


Percutaneous 
Vapor 6 


5 


1 c < f 


Unknown 


Moderate 


Mild effects 

(miosis, 

rhinorrhea) 


ECt 50 : 0.4 h 


N/A 


2 min 


Inhalation/Ocular 


10 


1.5 C 


Some 


Low 


NOTES 


a Based on Grotte and Yang (2001). 
b Bare skin. 

c See Appendix H for supporting toxici 
d Moderate temperatures (65-85°F). 
e Assumes personnel are masked with 
The TLE value is assumed 1 because 
g Hot temperatures (greater than 85°F 
h Based on recommendations for GB. 


ty profile estimates. 

eye protection and bare s 
3 the Ct profile is unknown 
)■ 


kin. 











e. GA Toxicity Estimates. Note that for an inhalation/ocular expouse the TLE is 
greater that 1. This means that the effective dosage increases with longer exposure 
durations and the concentration of the agent decreases. 

f. Sarin (GB) (see Table II-8 [page 11-18]). The Germans developed GB after they 
developed GA, 15 hence the designation GB. Pure GB is odorless and colorless. 13 It is a 
volatile liquid at room temperature. Unlike many other agents, for which clothing affords 
some protection against a liquid agent, clothing may enhance the potency of GB liquid on 
the skin. It is hypothesized that clothing retards evaporation, thereby increasing the 
effective dose. 10 See Table II-9 (page 11-20) for toxicity estimates. 



11-17 



Table 11-8. GB 



Alternate Designations: EA 1208; T-144 (German); Trilon 144 (German); Trilon 46 (German); T 46 German); TL-1618 
(UCTL); T-2106 (British); MFI; IMPF; Sarin II 


Chemical Name: Isopropyl methylphosphonofluoridate 


Synonyms: Fluorisoproopoxymethylphosphine oxide; Isopropyl methylfluorophosphate; Isopropyl 

methanefluorophosphonate; Isopropoxymethylphosphoryl fluoride; Propoxyl- 2 -methylphosphoryl fluoride; Phosphonofluridic 
acid, methyl-, isopropyl ester; Isopropylester kyseliny methylfluorfosfonove (Czech); O-lsopropyl methylphosphonofluoridate; 
Isopropyl-methylphosphoryl fluoride; Methylphosphonofluoridic acid isopropyl ester; Methylphosphonofluoridic acid 1- 
methylethyl ester; Phosphine oxide, fluoroisopropoxymethyl-; Phosphoric acid, methylfluoro-, isopropyl ester; 
Methylfluorphosphorsaeureisopropylester (German) 


CAS Registry Number: 107-44-8 


RTECS Number: TA8400000 


Physical and Chemical Properties 


Structural Formula: 

CH 3 
II I 
CH 3 — P— 0— CH 
I I 
F CH 3 

Molecular Formula: C4H10FO2P 
Molecular Weight: 140.09 


Physical State 


Colorless liquid 1 


Odor 


None when pure 2 


Boiling Point 


150°C (extrapolated) 3 


FP/MP 


-56°C (FP) 3_5 


Liquid Density (g/mL) 


Pure: 1.0887 @25°C; 1.1182 @ 0°C (extrapolated) 6 
Munitions grade: 1.0964 @ 25°C; 1.1255 @ 0°C (extrapolated) 6 


Vapor Density (relative to air) 


4.8 (calculated) 


Vapor Pressure (torr) 


2.48 x 10° @25°C; 4.10 x10" 1 @ 0°C 3 


Volatility (mg/m 3 ) 


1.87 x 10 4 @ 25 C C; 3.37 x 10 3 @ C C (calculated from vapor pressure) 3 


Latent Heat of Vaporization 
(kcal/mol) 


1 1 .6 @ 25 C C; 1 1 .7 @ 0°C (calculated from vapor pressure) 3 


Viscosity (cP) 


1 .397 @ 25.0°C, 2.583 @ 0°C (extrapolated) 7 


Viscosity of Vapor (cP) 


7.19 x10" 3 @ 25. 0°C, 5.51 x10" 3 @0°C 7 


Surface Tension (dynes/cm) 


25.9 @ 25.0°C, 28.8 @ 0°C (extrapolated) 7 


Flash Point 


Nonflammable 8 


Decomposition Temperature 


Complete decomposition occurs within 2 1/2 hr @ 150 C C 9 


Solubility 


Completely miscible with water and common organic solvents 1 ' 


Rate of Hydrolysis 


Varies with pH and temperature; at 20°C, t 1/2 = 27 min. @ pH 1 ; t 1/2 = 3 1/2 hr @ pH 
2; t 1/2 = 80 hr @ pH 7; ti/ 2 = 5.4 min @ pH 1 0; and t 1/2 = 0.6 min @ pH 1 1 . 10 


Hydrolysis Products 


Under acidic conditions, hydrogen fluoride (HF) and isopropyl methylphosphonic acid 
(IMPA) are formed which further hydrolyze to produce methylphosphonic acid (MPA) 
and isopropanol. Under alkaline conditions, methylfluorophosphonic acid (MFPA) 
and isopropyl alcohol are initially formed which further hydrolyze to produce MPA and 
HF. 11 


Stability in Storage 


GB stabilized with tributylamine can be stored in steel containers for at least 5 to 10 
years @ ambient temperature. At elevated temperatures up to 71 C C, storage life 
decreases slightly. 12 


Action on Metals or Other Materials 


At 71 °C, slightly corrosive on steel, copper, brass, inconel, K-monel, and lead as well 
as slight to severe amounts of corrosion on aluminum, depending on the type. 13 



1-18 



Table 11-8. GB (Continued) 



Other Data 



Skin and eye toxicity 



Eyes: very high; much greater through eyes than through skin; Skin: highly toxic; 
decontamination of smallest drop of liquid agent is essential; liquid penetrates skin 14 



Inhalation toxicity 



Most toxic route of exposure 15 



Rate of action 



Rapid 16 



Means of detection 



M8 paper, M9 paper, M256A1 CADK, M8A1 ACAA, M90 AMAD, M21 ACAA, M22 
ACADA, CAM/ICAM, M272 Water Testing Kit, , CAPDS, IPDS, AN/KAS-1 CWDD, 
" M18A2CADK, MM1 



Protection required 



MOPP4; liquid nerve agent penetrates ordinary clothing rapidly, clothing may 
enhance the potency of GB liquid on the skin 15 



Decontamination 



Flush eyes with water immediately. Use the M291 SDK to remove any liquid nerve 
agent on skin or clothing. Use the M295 IEDK for individual equipment. 14 STB is 
effective on equipment. Water, steam, and absorbents (earth, sawdust, ashes, and 
rags) are effective for physical removal. 1S 



Use 



Quick-acting casualty agent 



NOTES 

^ranke, S., Manual of Military Chemistry Volume I- Chemistry of Chemical Warfare Agents, ACSI-J-3890, Chemie der 

Kampfstoffe, East Berlin, April 1968, UNCLASSIFIED Report (AD849866). 

2 Welchman, R.M.A., Preliminary Report on the Potential Value of Nerve Gases as C.W. Agents, Porton Report No. 2747 

(PR 2747), Chemical Defence Experimental Establishment, Porton, England, January 1947, UNCLASSIFIED Report. 

3 Penski, Elwin C, The Properties of 2-Propyl Methylfluorophosphonate (GB) I. Vapor Pressure Data Review and Analysis, 

ERDEC-TR-166, USA Chemical and Biological Defense Command, Aberdeen Proving Ground, MD, June 1994, 

UNCLASSIED Report (ADB1 87225). 

4 Zeffert, B.M., et al., Slow Fractional Crystallization ofGB, CRLR 2, USA Chemical and Radiological Laboratories, Army 

Chemical Center, MD, April 1951, UNCLASSIFIED Report (AD498968). 

5 Tannenbaum, H., and Zeffert, B.M., Crystallization ofGB, TCIR-513, USA Chemical and Radiological Laboratories, Army 

Chemical Center, MD, November 1949, UNCLASSIFIED Report (ADE471275). 

6 Wardrop, A.W.H., and Bryant, P.J.R., Physico-Chemical Properties of Phosphorus Esters Part II: Some Constants of 

Isopropyl methylfluorophosphinate (GB), Porton Technical Paper No. 278 (PTP-278), Chemical Warfare Laboratories, Army 

Chemical Center, MD, March 1952, UNCLASSIFIED Report (ADE481544). 

7 Samuel, J.B., et al., Physical Properties of Standard Agents and Related Compounds at Several Temperatures (U), 

ARCSL-SP-83015, USA Armament Research and Development Command, Aberdeen Proving Ground, MD, June 1983, 

UNCLASSIFIED Report (ADC033491 ). 

8 Walpole, J.L., Determination of the Flash Points ofGA and GB, Porton Technical Paper No. 45 (PTP 45), Chemical 

Defence Experimental Establishment, Porton, England, March 1948, UNCLASSIFIED Report (ADE481350). 

9 Perry, B.J., et al., The Chemistry of the Alkylfluorophosphonites and Related Compounds, Porton Technical Paper No. 258, 

Chemical Defense Experimental Establishment, Porton, England, 31 August 1951. UNCLASSIFIED Report 

(ADE481528). 

Epstein, J., Studies on Hydrolysis ofGB I. Effect of pH and Temperature on Hydrolysis Rates. II. Observations on 
Hydrolysis ofGBin Sodium Bicarbonate Buffered Waters, MDR 132, Chemical Warfare Laboratories, Army Chemical 
Center, MD, February 1948, UNCLASSIFIED Report. 

11 Clark, D.N, Review of Reactions of Chemical Agents in Water, Final Report to USA Biomedical Research and 
Development Laboratory, Battelle, Columbus, OH, January 1989, UNCLASSIFIED Report (ADA213287). 
^Comparison of GA and GB as Chemical Warfare Agents (U), CWL-SP-1 , USA Chemical Warfare Laboratories, Army 
Chemical Center, MD, November 1957, UNCLASSIFIED Report. 

13 Hutchcraft, A.S. Jr., et al., Special Report: Corrosion Resistance of Metals Toward Isopropyl Methylphosphonofluoridate 
(GB), CRLR 510, USA Chemical and Radiological Laboratories, Army Chemical Center, MD, May 1955, UNCLASSIFIED 
Report (AD474404). 

14 FM 8-285/NAVMED P-5041/AFJMAN 44-149/FMFM 11-11, Treatment of Chemical Agent Casualties and Conventional 
Military Chemical Injuries, 22 December 1995. 

15 Sharon Reutter, et al., Rew'ew and Recommendations for Human Toxicity Estimates for FM 3-11.9, ECBC-TR-349, 
September 2003. 

^NIOSH-DOD-OSHA Sponsored Chemical and Biological Respiratory Protection Workshop Report, February 2000. 
17 DOD Chemical And Biological Defense Program Annual Report to Congress, Volume I, April 2003. 
18 FM 3-5/MCWP 3-37.3, NBC Decontamination, 28 July 2000. 



II-19 



g. GB Toxicity Estimates (Table II-9). Note that for an inhalation/ocular expouse 
the TLE is greater than 1. This means that the effective dosage increases with longer 
exposure durations and the concentration of the agent decreases. 

Table 11-9. GB Toxicity Estimates 10 



Endpoint 


Toxicity 
(mg-min/m 3 ) 


MV(L) 


Exposure 
Duration 


ROE 


Probit 
Slope 


TLE 


ROD 


DOC 


Lethality 


LD 50 : 1700 mg a 


N/A 


N/A; 70-kg 
man 


Percutaneous 
Liquid b 


5 


N/A 


Unknown 


Low 


LCt 50 : 35 a 


15 


2 min 


Inhalation/ 
Ocular 


12 


1.5 d 


Some 


Moderate 


LCt 50 : 12,000 ae 


N/A 


30-360 min 


Percutaneous 
Vapor f 


5 


-| d,g 


Unknown 


Low 


LCt 50 : 6000 hJ 
(provisional) 


N/A 


30-360 min 


Percutaneous 
Vapor f 


5 


-| d,g 


Unknown 


Low 


Severe effects, 
includes some 
deaths 


ED 50 : 1000 mg a 


N/A 


N/A; 70-kg 
man 


Percutaneous 
Liquid b 


5 


N/A 


Unknown 


Low 


ECt 50 : 25 a 


15 


2 min 


Inhalation/ 
Ocular 


12 


1.5 d 


Some 


Moderate 


ECt 50 : 8000 ae 


N/A 


30-360 min 


Percutaneous 
Vapor f 


5 


-| d,g 


Unknown 


Low 


ECt 50 : 4000 hJ 
(provisional) 


N/A 


30-360 min 


Percutaneous 
Vapor f 


5 


-| d,g 


Unknown 


Low 


Threshold 
effects (Slight 
ChE inhibition) 


ECt 50 : 1200 ae 


N/A 


30-360 min 


Percutaneous 
Vapor f 


5 


1 d,g 


Unknown 


Moderate 


ECt 50 : 600 hJ 
(provisional) 


N/A 


30-360 min 


Percutaneous 
Vapor f 


5 


■\ d,g 


Unknown 


Low 


Mild effects 

(miosis, 

rhinorrhea) 


ECt 50 : 0.4 ' 


N/A 


2 min 


Inhalation/ 
Ocular 


10 


1.5 dli 


Some 


Moderate 


NOTES 


a Based on Grotte and Yang (2001). 

"Bare skin. 

C LD 50 could be less with clothing. 

d See Appendix H for supporting toxicity profile estir 

e Moderate temperatures (65-85°F) 

'Assumes personnel are masked with eye protectio 

g The TLE value is assumed 1 because the concen 

h Hot temperatures (greater than 85°F) 

Based on Grotte and Yang (2001) and Letter (25 Iv 

'Based on human data and recent rat data of Miodi 


nates. 

n and bare skin 
ration-time prol 

1ar 03). 
szewski et al. ( 


le is unknown. 
2002). 











h. GD (see Table 11-10). GD is a colorless liquid when pure. 13 2 PAM CI is not as 
effective for GD poisoning as it is for other nerve agents 1 because the "aging" process half- 
time is within 2 minutes. 15 See Table 11-11 (page 11-23) for toxicity estimates. 



11-20 



Table 11-10. GD 



Alternate Designations: EA 1210 (US); Zoman (USSR); T-2107 (British, UK); Trilon (German); PMFP 


Chemical Name: Pinacolyl methyl phosphonofluoridate 


Synonyms: 3,3-Dimethyl-n-but-2-yl methylphosphonofluoridate; 3,3-Dimethyl-2-butyl methylphosphonofluridate; 2-Butanol, 
3,3-dimethyl-, methylphosphonofluoridate; Methylphosphonofluoridic acid, 3,3-dimethyl-2-butyl ester; 1,2,2-Trimethylpropyl 
methyphosphonofluoridate; 1 ,2,2-Trimethylpropylester kyseliny methylfluorfosfonove (Czech); Methylphosphonofluoridic 
acid 1 ,2,2-trimethylpropyl ester; Phosphonofluoridic acid, methyl-, 1,2,2-trimethylpropyl ester; Phosphine oxide, fluoromethyl 
(1,2,2-trimethylpropoxy)-; Methyl pinacolyl phosphonofluoridate; Pinacolyl methylfluorophosphonate; 
Fluoromethylpinacolyloxyphosphine oxide; Methyl pinacolyloxyfluorophosphine oxide; Pinacolyl methane 
fluorophosphonate; Pinacoloxymethylphosphoryl fluoride; Methylfluoropinacolylphosphonite; 
Methylfluorphosphorsaeurepinakolylester (German); Methyl pinacolyloxy phosphorylfluoride; Methyl pinacolyl 
phosphonofluoridate; Pinacoloxymethylphosphoryl fluoride; Pinacolyl methylphosphonofluoride; Pinacolyloxy 
methylphosphoryl fluoride; Pynacolyl methylfluorophosphonate 


CAS Registry Number: 96-64-0 


RTECS Number: TA8750000 


Physical and Chemical Properties 


Structural Formula: 

CH 3 

II I 
CHo — P — 0— CH— C— CH 3 
I II 
F CH3 CH3 

Molecular Formula: C7H16FO2P 
Molecular Weight: 182.17 


Physical State 


Colorless liquid when pure 1 


Odor 


Fruity; impurities give it the odor of camphor 2 ' 3 


Boiling Point 


198°C (extrapolated) decomposes 4 


FP/MP 


-42°C (MP); 5,e generally solidifies to a noncrystalline, glasslike material 7 


Liquid Density (g/mL) 


1.0222 @ 25°C; 1.0456 @ 0°C (extrapolated) 7 


Vapor Density (relative to air) 


6.3 (calculated) 


Vapor Pressure (torr) 


4.01 x 10" 1 @ 25°C; 4.96 x 10" 2 @ 0°C 4 


Volatility (mg/m 3 ) 


3.93 x 10 3 @ 25°C; 5.31 x 10 2 @ 0°C (calculated from vapor pressure) 4 


Latent Heat of Vaporization 
(kcal/mol) 


13.2 @ 25°C; 13.8 @ 0°C (calculated from vapor pressure) 4 


Viscosity (cP) 


3.167 @ 25.0°C, 6.789 @ 0°C (extrapolated) 5 


Viscosity of Vapor (cP) 


5.90 x 10" 3 @ 25.0°C, 5.33 x 10" 3 @ 0°C 5 


Surface Tension (dynes/cm) 


24.5 @ 25.5°C 5 


Flash Point 


121°C (open cup) 5 ' 8 


Decomposition Temperature 


Above 150°C, 1 stabilized GD decomposes in 200 hrs @ 130°C; unstabilized GD 
decomposes in 4 hrs @ 130°C 9 


Solubility 


Solubility of GD in water is 2.1 g GD/100g @ 20°C; 9 ' 10 3.4 g GD/100g solution @ 
0°C; 9 very soluble in organic solvents 1 


Rate of Hydrolysis 


Varies with pH; using a 0.003 molar solution of GD @ 25°C, t 1/2 = 3 hr. @ pH 2; t 1/2 
= 45 hrs @ pH 6.65; ty 2 = 60 hrs @ pH 10; complete hydrolysis occurs in less than 
5 min in a 5% NaOH solution 11 


Hydrolysis Products 


Essentially PMPA and HF 11 


Stability in Storage 


Relatively stable in glass for 5-1/2 months @ ambient temperature with or without a 
stabilizer. 12 Stabilized GD can be stored for at least 6 months @ elevated 
temperatures (71°C) in glass, steel, and aluminum containers. 13 


Action on Metals or Other Materials 


Corrosion rate on steel is 0.00001 inch/month @ 65 C C 14 



II-21 



Table 11-10. GD (Continued) 



Other Data 



Eyes: very high toxicity; much greater through eyes than through skin. Skin: highly toxic; 
decontamination of smallest drop of liquid agent is essential; liquid penetrates skin. 15 



Skin and eye toxicity 



Inhalation toxicity 



Most toxic route of exposure 



Rate of action 



Rapid 



Means of detection 



M8 paper, M9 paper, M256A1 CADK, M8A1 ACAA, M90 AMAD, M21 ACAA, M22 
ACADA, CAM/ICAM, M272 Water Testing Kit, , CAPDS, IPDS, AN/KAS-1 CWDD, 
M18A3 CADK, 16 M18A2 CADK, MM1 



Protection required 



MOPP4; liquid nerve agents penetrate ordinary clothing rapidly 



Decontamination 



Flush eyes with water immediately. Use the M291 SDK to remove any liquid nerve 
agent on skin or clothing. Use the M295 IEDK for individual equipment. 15 STB is 
effective on equipment. Water, steam, and absorbents (earth, sawdust, ashes, and 
rags) are effective for physical removal. 19 



Use 



Quick-acting casualty agent 



NOTES 



1 Franke, S., Manual of Chemistry Volume I- Chemistry of Chemical Warfare Agents, ACSI-J-3890, Chemie der Kampfstoffe, East 

Berlin, April 1968, UNCLASSIFIED Technical Manual (AD849866). 

2 Welchman, R.M.A., Preliminary Report on the Potential Value of Nerve Gases as C.W. Agents, Porton Report No. 2747 (PR 2747), 

Chemical Defence Experimental Establishment, Porton, England, January 1947, UNCLASSIFIED Report (ADE470188). 

3 TM 3-215/AFM 355-7, Military Chemistry and Chemical Agents, December 1963, UNCLASSIFIED Technical Manual 

(ADA292141). 

"Savage, J. J., and Fielder, D., The Vapor Pressure of Chemical Agents CD, VX, EA2223, EA 3547, EA 3580, EA 5365, and EA 

5533, EC-TR-76058, Aberdeen Proving Ground, MD, August 1976, UNCLASSIFIED Report (ADB013164). 

5 Samuel, J.B., et al., Physical Properties of Standard Agents, Candidate Agents, and Related Compounds at Several Temperatures 

(U), ARCSL-SP-83015, USA Armament Research and Development Command, Aberdeen Proving Ground, MD, June 1983, 

UNCLASSIFIED Report (ADC033491). 

6 Stern, R.A., USA Chemical Research and Development Laboratories Notebook # NB 7265, p. 45 (C). 

7 Zeffert, B.M., and Coulter, P.B., Physical Constants ofG-Series Compounds: Compounds EA 1210, EA 1211, EA 1212, EA 1213, 

EA 1214, Technical Division Memorandum Report 1292, USA Chemical Research and Development Laboratories, Army Chemical 

Center, MD, July 1947, UNCLASSIFIED Report (ADB964904). 

"Fielder, D, USA Chemical Warfare Laboratories Notebook # NB 6695, p. 72 (C). 

9 Chemical Agent Data Sheets Volume I, Edgewood Arsenal Special Report EO-SR-74001, Edgewood Arsenal, Aberdeen Proving 

Ground, MD, December 1974, UNCLASSIFIED Report (ADB028222). 

10 Witten, Benjamin, The Search for Toxic Chemical Agents (U), EATR 4210, Edgewood Arsenal Research Laboratories, MD, 

November 1969, UNCLASSIFIED Report (AD507852). 

"Buckles, L.C., The Hydrolysis Rate of GD, TCIR 373, Chemical Corps Technical Command, Army Chemical Center, MD, March 

1947, UNCLASSIFIED Report (ADB966291). 

"Newman, J.H., etal.,/4 Thickener for GD (U), EC-TR-77016, Edgewood Arsenal, Aberdeen Proving Ground, MD, April 1977, 

CONFIDENTIAL Report (ADC009719). 

"Grula, R.S., et al., Storage Stability of GD, GF and EA 1356 (U), CRDLR 3342, USA Chemical Research and Development 

Laboratories, Edgewood Arsenal, MD, December 1965, CONFIDENTIAL Report (AD369299). 

"Hormats, S., et al., Storage Stability in Steel at 65°C of Pure GD. Corrosion Rate of Steel at 65°C, TDMR 1 346, Chemical Corps 

Technical Compound, Army Chemical Center, MD, March 1948, UNCLASSIFIED Report (ADB964759). 

15 FM 8-285/NAVMED P-5041/AFJMAN 44-149/FMFM 11-11, Treatment of Chemical Agent Casualties and Conventional Military 

Chemical Injuries, 22 December 1995. 

16 Sharon Reutter, et al., SBCCOM Report Review and Recommendations for Human Toxicity Estimates for FM 3-11.9, ECBC-TR- 

349, September 2003. 

17 NIOSH-DOD-OSHA Sponsored Chemical and Biological Respiratory Protection Workshop Report, February 2000. 

18 DOD Chemical And Biological Defense Program Annual Report to Congress, Volume I, April 2003. 

19 FM 3-5/MCWP 3-37.3, NBC Decontamination, 28 July 2000. 



11-22 



i. GD Toxicity Estimates (Table 11-11). Note that for an inhalation/ocular expouse 
the TLE is greater than 1. This means that the effective dosage increases with longer 
exposure durations and the concentration of the agent decreases. 

Table 11-11. GD Toxicity Estimates 10 



Endpoint 


Toxicity 
(mg-min/m 3 ) 


MV(L) 


Exposure 
Duration 


ROE 


Probit 
Slope 


TLE 


ROD 


DOC 


Lethality 


LD 50 : 350 mg a 


N/A 


N/A; 70-kg 
man 


Percutaneous 
Liquid b 


6 


N/A 


Unknown 


Low 


LCt 50 : 35 a 


15 


2 min 


Inhalation/ 
Ocular 


12 


1.25° 


Some 


Low 


LCt 50 : 3000 a ' d 


N/A 


30-360 min 


Percutaneous 
Vapor e 


6 


1*' 


Unknown 


Low 


LCt 50 : 1500 gh 
(provisional) 


N/A 


30-360 min 


Percutaneous 
Vapor e 


6 


r 1 


Unknown 


Low 


Severe effects, 
includes some 
deaths 


ED 50 : 200 mg a 


N/A 


N/A; 70-kg 
man 


Percutaneous 
Liquid b 


6 


N/A 


Unknown 


Low 


ECt 5 „: 25 a 


15 


2 min 


Inhalation/ 
Ocular 


12 


1.25 c 


Some 


Low 


ECt 50 : 2000 ad 


N/A 


30-360 min 


Percutaneous 
Vapor e 


6 


1*' 


Unknown 


Low 


ECt 50 : 1000 gh 
(provisional) 


N/A 


30-360 min 


Percutaneous 
Vapor e 


6 


1*' 


Unknown 


Low 


Threshold 
effects 


ECt 50 : 300 ad 


N/A 


30-360 min 


Percutaneous 
Vapor e 


6 


1 c '< 


Unknown 


Low 


ECt 50 : 150 gh 
(provisional) 


N/A 


30-360 min 


Percutaneous 
Vapor 6 


6 


1 el 


Unknown 


Low 


Mild effects 

(miosis, 

rhinorrhea) 


ECt 5 „: 0.2 ' 


N/A 


2 min 


Inhalation/ 
Ocular 


10 


1.4 C 


Some 


Low 


NOTES 


a Based on Grotte and Yang (2001). 
b Bare skin. 

"See Appendix H for supporting toxicity p 
d Moderate temperatures (65-85°F). 
e Assumes personnel are masked with 
f The TLE value is assumed 1 because th< 
g Based on recommendations for GB. 
h Hot temperatures (greater than 85°F). 
'Based on recommendations for GB and r 


■ofile estimates. 

aye protection and bare skin. 

3 concentration time profile is unknown. 

elative potency of GD and GB. 











j. Cyclosarin (GF) (see Table 11-12 [page 11-24]). GF is a colorless and odorless 
liquid when pure. 13 See Table 11-13 (page 11-26) for toxicity estimates. 



11-23 



Table 11-12. GF 



Alternate Designations: EA 1212 (US); T-2139 (British); CMPF 


Chemical Name: Cyclohexyl methylphosphonofluoridate 


Synonyms: Cyclohexyloxyfluoromethylphosphine oxide; Cyclohexyl methylfluorophosphate; Phosphonofluoridic acid, 
methyl-, cyclohexyl ester; Methyl cyclohexylfluorophosphonate 


CAS Registry Number: 329-99-7 


RTECS Number: TA 8225000 


Physical and Chemical Properties 


Structural Formula: 


o 




CH 3 — P-O^ \ 


Molecular Formula: C 7 H 14 F0 2 P 
Molecular Weight: 180.16 


h 


Physical State 


Colorless liquid 1 


Odor 


None if pure 2 


Boiling Point 


228°C (extrapolated) 3 


FP/MP 


-30 to-50°C (FP); 4 -12°C (MP); below -30°C, a metastable crystalline form of GF 
is produced which slowly converts into a stable form that melts @ -12°C 5 


Liquid Density (g/mL) 


1.1276 @ 25°C; 1.1525 @ 0°C (extrapolated) 4 


Vapor Density (relative to air) 


6.2 (calculated) 


Vapor Pressure (torr) 


9.27 x 10' 2 @ 25°C; 9.78 x 10" 3 @ 0°C (extrapolated) 3 


Volatility (mg/m 3 ) 


8.98 x 10 2 @ 25°C; 1.03 x 10 2 @ 0°C (calculated from vapor pressure) 3 


Latent Heat of Vaporization 
(kcal/mol) 


14.3 @ 25°C; 14.8 @ C C (calculated from vapor pressure) 3 


Flash Point 


94°C 6 


Viscosity (cP) 


5.41 @ 25.0°C, 14.762 @ 0°C (extrapolated) 6 


Viscosity of Vapor (cP) 


6.15 x 10" 3 @ 25.0°C, 5.5 x 10" 3 @ 0°C 6 


Surface Tension (dynes/cm) 


32.3 @ 25.5°C 6 


Decomposition Temperature 


Completely decomposes within 2 hrs @ 150°C 7 


Solubility 


Solubility in water is 3.7 g GF/100g @ 20°C; 5.1 g GF/100 g @ 0°C 6 


Rate of Hydrolysis 


ti /2 = 42 hrs @ 25°C using a 0.003 M solution of GF in distilled water 8 


Hydrolysis Products 


Hydrogen fluoride and cyclohexyl methylphosphonic acid 5 


Stability in Storage 


Stabilized GF can be stored @ 71 C C for at least 6 months in glass containers and at 
least 1 year in steel and aluminum containers. 9 


Action on Metals or Other Materials 


Corrosion rate on steel is 0.000053 inch/month @ 65°C 10 


Other Data 


Skin and eye toxicity 


Eyes: very high toxicity; much greater through eyes than through skin. Skin: highly 
toxic; decontamination of smallest drop of liquid agent is essential; liquid penetrates 
skin 11 . 


Inhalation toxicity 


Most toxic route of exposure 12 


Rate of action 


Rapid 13 


Means of detection 


M8 paper, M9 paper, M256A1 CADK, M8A1 ACAA, M90 AMAD, M21 ACAA, M22 
ACADA, CAM/ICAM, M272 Water Testing Kit, , CAPDS, IPDS, AN/KAS-1 CWDD 
M18A3 CADK, 14 M18A2 CADK, MM1 


Protection required 


MOPP4; liquid nerve agents penetrate ordinary clothing rapidly 11 . 


Decontamination 


Flush eyes with water immediately. Use the M291 SDK to remove any liquid nerve 
agent on skin or clothing. Use the M295 IEDK for individual equipment. 11 STB is 
effective on equipment. Water, steam, and absorbents (earth, sawdust, ashes, and 
rags) are effective for physical removal. 15 


Use 


Quick-acting casualty agent 



II-24 



Table 11-12. GF (Continued) 



NOTES 

''Eakle, B.F., Chemical Agent GF (U), Technical Study 69-C4, USA Desert Test Center, Fort Douglas, Utah, January 1969, 
UNCLASSIFIED Report (AD509689). 

2 Chemical Agent Data Sheets Vol. II, Edgewood Arsenal Special Report EO-SR-74002, USA Armament Command, 
Edgewood Arsenal, Aberdeen Proving Ground, MD, December 1974, CONFIDENTIAL Report (AD000020). 
3 Tevault, D.E., et al., Vapor Pressure of GF, TR-304S, USA ECBC, Aberdeen Proving Ground, MD, submitted for 
publication 2 May 2003, UNCLASSIFIED Report. 

4 Zeffert, B.M., and Coulter, P.B., Physical Constants ofG-Series Compounds: EA1210, EA1211, EA1212, EA1213, EA1214, 
Technical Division Memorandum Report 1292), July 1947, USA Chemical Research and Development Laboratories, Army 
Chemical Center, MD, July 1947, UNCLASSIFIED Report (ADB964904). 

5 Chinn, Kenneth, S. K., Joint CB Technical Data Source Book, Volume III, G Nerve Agents, Part Three: Agents GD and GF 
(U), DPG-TR-82-004, USA Dugway Proving Ground, Utah, August 1983, SECRET Report (ADC032927). 
Samuel, J.B., et al., Physical Properties of Standard Agents, Candidate Agents, and Related Compounds at Several 
Temperatures (U), ARCSL-SP-83015, USA Armament Research and Development Command, Aberdeen Proving Ground, 
MD, June 1 983, UNCLASSIFIED Report (ADC033491 ). 

7 Perry, B.J., et al., The Chemistry of the Alkylfluorophosphonites and Related Compounds, Porton Technical Paper No. 258, 
Chemical Defense Experimental Establishment, Porton, England, 31 August 1951, UNCLASSIFIED Report (ADE481528). 
8 Buckles, L.C., The Hydrolysis Rate of G Agents, TCIR 393, USA Chemical Research and Development Laboratories, Army 
Chemical Center, MD, December 1947, UNCLASSIFIED Report (ADB966236). 

9 Grula, R.S., et al., Storage Stability of GD, GF and EA 1356 (U), CRDLR 3342, USA Chemical Research and Development 
Laboratories, Edgewood Arsenal, MD, December 1965, CONFIDENTIAL Report (AD369299). 

10 Kaiser, W.A., Summary of Information on Agent GF, CRLR 164, USA Chemical Research and Development Laboratories, 
Army Chemical Center, MD, March 1954, UNCLASSIFIED Report (ADB969120). 

11 FM 8-285/NAVMED P-5041/AFJMAN 44-149/FMFM 11-11, Treatment of Chemical Agent Casualties and Conventional 
Military Chemical Injuries, 22 December 1995. 

12 Sharon Reutter, et al., Rew'ew and Recommendations for Human Toxicity Estimates for FM 3-11.9, ECBC-TR-349, 
September 2003. 

n NIOSH-DOD-OSHA Sponsored Chemical and Biological Respiratory Protection Workshop Report, February 2000. 
14 DOD Chemical And Biological Defense Program Annual Report to Congress, Volume I, April 2003. 
15 FM 3-5/MCWP 3-37.3, NBC Decontamination, 28 July 2000. 

k. GF Toxicity Estimates (Table 11-13, page 11-26). Note that for an 
inhalation/ocular exposure the TLE is greater than 1. This means that the effective dosage 
increases with longer exposure durations and the concentration of the agent decreases. 



-25 







Table II-13. GF Toxicity Estimates 1 " 








Endpoint 


Toxicity 
(mg-min/m 3 ) 


MV(L) 


Exposure 
Duration 


ROE 


Probit 
Slope 


TLE 


ROD 


DOC 


Lethality 


LD 50 : 350 mg 

a 


N/A 


N/A; 70-kg 
man 


Percutaneous 
Liquid" 


5 


N/A 


Unknown 


Low 


LCt 50 : 35 a 


15 


2 min 


Inhalation/ 
Ocular 


12 


1.25 c 


Some 


Moderate 


LCt 50 : 3000 ad 


N/A 


30-360 min 


Percutaneous 
Vapor e 


5 


1 c,f 


Unknown 


Low 


LCt 50 : 1500 gh 
(provisional) 


N/A 


30-360 min 


Percutaneous 
Vapor e 


5 


1 c,f 


Unknown 


Low 


Severe effects, 
includes some 
deaths 


ED 50 : 200 mg 

a 


N/A 


N/A; 70-kg 
man 


Percutaneous 
Liquid" 


5 


N/A 


Unknown 


Low 


ECt 50 25 a 


15 


2 min 


Inhalation/ 
Ocular 


12 


1.25 c 


Some 


Moderate 


ECt 50 : 2000 ad 


N/A 


30-360 min 


Percutaneous 
Vapor e 


5 


1 c,f 


Unknown 


Low 


ECt 50 1000 gh 
(provisional) 


N/A 


30-360 min 


Percutaneous 
Vapor e 


5 


1 c,f 


Unknown 


Low 


Threshold 
effects 


ECt 50 : 300 ad 


N/A 


30-360 min 


Percutaneous 
Vapor e 


6 


1 c,f 


Unknown 


Low 


ECt 50 : 150 gh 
(provisional) 


N/A 


30-360 min 


Percutaneous 
Vapor e 


6 


1 c,f 


Unknown 


Low 


Mild effects 

(miosis, 

rhinorrhea) 


ECt 50 : 0.2' 


N/A 


2 min 


Inhalation/ 
Ocular 


10 


1.4 c 


Some 


Low 


NOTES 


a Based on Grotte and Yang (2001). 

b Bare skin. 

c See Appendix H for supporting toxicity profile estimates. 

"Moderate temperatures (65-85°F). 

e Assumes personnel are masked with eye protection and bare skin. 

f The TLE value is assumed to be 1 because the Ct profile is unknown. 

g Hot temperatures (greater than 85°F). 

h Based on recommendations for GB. 

'Based on recommendations for GD. 



1. O-ethyl methyl phosphonothiolate (VX) (see Table 11-14). VX is a colorless and 
odorless liquid when pure. 13 Although VX is significantly less volatile than the other 
agents, it does vaporize to some extent and is extremely potent. A significant component of 
the hazard or airborne VX is percutaneous absorption of the vapor. 10 See Table 11-15 (page 
11-29) for toxicity estimates. 



11-26 



Table 11-14. VX 



Alternate Designations: EA 1701; TX60 


Chemical Name: 0-Ethyl-S-(2-diisopropylaminoethyl) methyl phosphonothiolate 


Synonyms: S-(2-Diisopropylaminoethyl) O-ethyl methyl phosphonothiolate; Ethyl-S-dimethylaminoethyl 
methylphosphonothiolate; Phosphonothioic acid, methyl-, S-(2-(diisopropylamino)ethyl) O-ethyl ester; Ethyl S-2- 
diisopropylaminoethyl methylphosphonothiolate; Ethyl-S-diisopropylaminoethyl methylthiophosphonate; 
Methylphosphonothioic acid S-(2- (bis(methylethyl)amino)ethyl) O-ethyl ester; O-Ethyl-S-2-diisopropylaminoethylester 
kyseliny methylthiofosfonove (Czech) 


CAS Registry Number: 50782-69-9 


RTECS Number: TB1 090000 


Physical and Chemical Properties 


Structural Formula: 

II CH(CH 3 ) 2 
CH 3 CH 2 — O— P— S— CH 2 CH 2 — N 

CH 3 X CH(CH 3 ) 2 

Molecular Formula: CnH 2 6N0 2 PS 
Molecular Weight: 267.37 


Physical State 


Colorless liquid when pure 1 


Odor 


Odorless when pure 1 


Boiling Point 


292°C (extrapolated) 2 


FP/MP 


Below -51 °C and -39 to -60°C (FP) 3 " 5 


Liquid Density (g/mL) 


1 .0083 @ 25°C; 1 .0209 @ 0°C (extrapolated) 4 


Vapor Density (relative to air) 


9.2 (calculated) 


Vapor Pressure (torr) 


8.78 x 10" 4 @ 25°C; 4.22 x 10" 5 @ 0°C (extrapolated) 2 


Volatility (mg/m 3 ) 


1.26 x 10 1 @ 25°C; 6.62 x 10" 1 @ C C (calculated from vapor pressure) 2 


Latent Heat of Vaporization 
(kcal/mol) 


19.2 @ 25°C; 20.1 @ C C; (calculated from vapor pressure) 2 ' 6 


Viscosity (cP) 


10.041 @ 25.0°C, 37.532 @ 0°C (extrapolated) 3 


Viscosity of Vapor (cP) 


5.13 x 10" 3 @ 25.0°C, 4.63 x 10" 3 @ 0°C 3 


Surface Tension (dynes/cm) 


31.3 @ 25. 0°C, 37.7 @0°C 3 


Flash Point 


127°C (continuously closed cup method) 7 


Decomposition Temperature 


t 1/2 = 502 days @ 71 °C; t 1/2 = 41 days @ 100°C; t 1/2 = 34.5 hrs @ 150°C; t 1/2 = 10 
hrs @ 1 70°C; 8 t 1/2 = 1 .6 hrs @ 200°C; t 1/2 = 4 min @ 250°C; t 1/2 = 36 sec @ 295°C 5 


Solubility 


Water solubility of VX is 5% @ 21 .5°C; 4 miscible with water below 9.4°C; 4 soluble 
in common organic solvents 5 


Rate of Hydrolysis 


Hydrolysis rate of VX varies with temperature and concentration. At 22°C, ti/ 2 = 1.8 
min[1.25M NaOH]; t 1/2 = 10.8 min [0.25M NaOH]; t 1/2 = 31 min. [0.10M NaOH]; t 1/2 = 
3.3 hrs [0.01 M NaOH]; t 1/2 = 20.8 hrs [0.001 M NaOH]; and t 1/2 = 60 hrs [pure H 2 0] 9 


Hydrolysis Products 


VX hydrolyzes via three different pathways (P-S, P-O, and C-S), which vary 
significantly with temperature and pH. At pH below 12, the P-O bond cleavage path 
produces ethyl methylphosphonate (EMPA) and the toxic S-[2- 
diisopropylaminoethyl] methylphosphonothiolate ion (EA 2192). At room 
temperature EA 2192 reacts very slowly with OH" [EA 2192, t 1/2 = 7.4 days (1 .0M 
NaOH)] eventually producing less toxic products. ,1 ° Using an equimolar ratio of 
VX and water at elevated temperatures appears to reduce the persistency of EA 
2192. 11 


Stability in Storage 


Relatively stable @ ambient temperature; unstabilized VX of 95% purity 
decomposes at a rate of 5% a month @ 71 °C. 13 Highly purified VX is stable in both 
glass and steel. 1 


Action on Metals or Other Materials 


Negligible on brass, steel, and aluminum; slight corrosion with copper 12 



II-27 



Table 11-14. VX (Continued) 



Other Data 



Skin and eye toxicity 



Extremely toxic by skin and eye absorption 14 



Inhalation toxicity 



Extremely potent 15 



ROA 



Rapid 16 



Means of detection 



M8 paper, M9 paper, M256A1 CADK, M8A1 ACAA, M90 AMAD, M22 ACADA, 
CAM/ICAM, M272 Water Testing Kit, CAPDS, IPDS, AN/KAS-1 CWDD, M18A3 
CADK, 17 M18A2 CADK, MM1 



Protection required 



MOPP4; liquid nerve agents penetrate ordinary clothing rapidly 14 



Decontamination 



Flush eyes with water immediately. Use the M291 SDK to remove any liquid nerve 
agent on skin or clothing. Use the M295 IEDK for individual equipment. 14 STB, 
HTH, or household bleach are effective on equipment. Water, soaps, detergents, 
steam, and absorbents (earth, sawdust, ashes, and rags) are effective for physical 



Use 



Quick-acting casualty agent 



NOTES 

1 Witten, B., The Search for Toxic Chemical Agents (U), EATR 4210, Edgewood Arsenal Research Laboratories, MD, 

November 1969, UNCLASSIFIED Report (AD507852). 

2 Buchanan, J.H., et al., Vapor Pressure of VX, ECBC-TR-068, USA Soldier and Biological Chemical Command, Aberdeen 

Proving Ground, MD, November 1999, UNCLASSIFIED Report (ADA371297). 

3 Samuel, J.B., et al., Physical Properties of Standard Agents, Candidate Agents, and Related Compounds at Several 

Temperatures (U), ARCSL-SP-83015, June 1983, USA Armament Research and Development Command, Aberdeen 

Proving Ground, MD, UNCLASSIFIED Report (ADC033491). 

4 Coulter, P.B., et al., Physical Constants of Thirteen V Agents, CWLR 2346, USA Chemical Warfare Laboratories, Army 

Chemical Center, MD, December 1959, UNCLASSIFIED Report (AD314520). 

~ 'Chemical Agent Data Sheets Volume I, Edgewood Arsenal Special Report EO-SR-74001 , USA Armament Command, 

Edgewood Arsenal, Aberdeen Proving Ground, MD, December 1974, UNCLASSIFIED Report (ADB028222). 

6 Abercrombie, P., ECBC Notebook* NB 98-0079, p. 11 (U). 

7 Butrow, B., ECBC Notebook # NB 97-0109 (C). 

8 Rohrbaugh, D.K., et al., Studies in Support of SUPLECAM (Surveillance Program for Lethal Chemical Agents and 

Munitions) II, 1. Thermal Decomposition ofVX, CRDEC-TR-88056, USA Chemical Research, Development and Engineering 

Center, Aberdeen Proving Ground, MD, May 1988, UNCLASSIFIED Report (ADB124301). 

9 Yang, Y, et al., "Hydrolysis of VX: Activation Energies and Autocatalysis," In Proceedings of the 1994 ERDEC Scientific 

Conference on Chemical Biological Defense Research 15-18 Novemberl994, UNCLASSIFIED Paper (ADE479900), 

ERDEC-SP-036, pp. 375-382, USA Edgewood Research, Development and Engineering Center, Aberdeen Proving 

Ground, MD, May 1996, UNCLASSFIED Report (ADA313080). 

10 Yang, Y., etal., "Perhydrolysis of Nerve Agent VX," J. Org. Chem, Vol. 58, p. 6965, 1993. 

11 Yang, Y., et al., "Hydrolysis of VX with Equimolar Water at Elevated Temperatures: Activation Parameters of VX, CV and 

EA 2192," In Proceedings of the 1996 ERDEC Scientific Conference on Chemical Biological Defense Research 19-22 

Novemberl996, UNCLASSIFIED Paper (ADE487572), ERDEC-SP-048, pp. 599-605, USA Edgewood Research, 

Development and Engineering Center, Aberdeen Proving Ground, MD, October 1997, UNCLASSFIED Report 

(ADA334105). 

Eckhaus, S.R., et al., Resistance of Various Materials of Construction in Contact with Transester Process^ CWL Technical 
Memorandum 31-73, USA Chemical Research and Development Laboratories, Army Chemical Center, MD, February 1959, 
UNCLASSIFIED Report (ADB963125). 

13 Salamon, M.K., Agent VX, CWL Special Publication 4-10, USA Chemical Warfare Laboratories, Army Chemical Center, 
MD, June 1959, UNCLASSIFIED Report (ADE471 109). 

14 FM 8-285/NAVMED P-5041/AFJMAN 44-149/FMFM 11-11, Treatment of Chemical Agent Casualties and Conventional 
Military Chemical Injuries, 22 December 1995. 

15 Sharon Reutter, et al., Review and Recommendations for Human Toxicity Estimates for FM 3-11.9, ECBC-TR-349, 
September 2003. 

1B NIOSH-DOD-OSHA Sponsored Chemical and Biological Respiratory Protection Workshop Report, February 2000. 
17 DOD Chemical And Biological Defense Program Annual Report to Congress, Volume I, April 2003. 
18 FM 3-5/MCWP 3-37.3, NBC Decontamination, 28 July 2000. 

m. VX Toxicity Estimates (see Table 11-15). VX is unlike the G agents in that the Ct 
profile for vapor inhalation appears to obey Haber's Law. However, some data indicates 
that the TLE may be less than one. If it does obey the toxic load principle (C n t = k) where 
the TLE (n) is less than one, it means that the ECtso does not increase with longer 
exposures at lower concentrations; in fact, it may actually decrease. 9 



11-28 







Table II-15. VX Toxicity Estimates 10 








Endpoint 


Toxicity 
(mg-min/m 3 ) 


MV(L) 


Exposure 
Duration 


ROE 


Probit 
Slope 


TLE 


ROD 


DOC 


Lethality 


LD 50 : 5mg a 


N/A 


N/A; 70-kg 
man 


Percutaneous 
Liquid" 


6 


N/A 


Unknown 


Low 


LCt 50 : 15 a 


15 


2-360 min 


Inhalation/ 
Ocular 


6 


1 c 


Little, if any 


Low d 


LCt 50 : 150 ae 


N/A 


30-360 min 


Percutaneous 
Vapor f 


6 


1 eg 


Little, if any 


Low 


LCt 50 : 75 M 
(Provisional) 


N/A 


30-360 min 


Percutaneous 
Vapor f 


5 


1 eg 


Little, if any 


Low 


Severe effects, 
includes some 
deaths 


ED 50 : 2mg a 


N/A 


N/A; 70-kg 
man 


Percutaneous 
Liquid" 


6 


N/A 


Unknown 


Low 


ECt 50 : 10 a 


15 


2-360 min 


Inhalation/ 
Ocular 


6 


1 c 


Little, if 
any 


Low d 


ECt 50 : 25 ae 


N/A 


30-360 min 


Percutaneous 
Vapor f 


6 


1 c,g 


Unknown 


Moderate 


ECt 50 : 12 hJ 
(Provisional) 


N/A 


30-360 min 


Percutaneous 
Vapor f 


6 


1 c,g 


Unknown 


Low 


Threshold effects 
(Slight ChE 
inhibition) 


ECt 50 : 10 a ' 9 


N/A 


30-360 min 


Percutaneous 
Vapor' 


6 


1 c,g 


Unknown 


Moderate 


ECt 50 : 5 hJ 


N/A 


30-360 min 


Percutaneous 
Vapor f 


6 


1 c,g 


Unknown 


Low 


Mild effects 

(miosis, 

rhinorrhea) 


ECt 50 : 0.1 a 


N/A 


2-360 min 


Inhalation/ 
Ocular 


4 


1 c,g,j 


Some 


Low 


NOTES 


a Based on Grotte and Yang (2001). 

b Bare skin. 

c See Appendix H for supporting toxicity profile estimates. 

d LCt 50 /ECt 50 could be less. 

e Moderate temperatures (65-85°F). 

'Assumes personnel are masked with eye protection and bare skin. 

9 The TLE value is assumed to be 1 because the Ct profile is unknown. 

h Hot temperatures (greater than 85°F). 

'Based on recommendations for GB and Cummings and Craig (1965). 

'Estimates should be revised as new data becomes available; human estimate for miosis may go down. 



n. Vx (see Table 11-16) [page 11-30]. Another V agent of interest is V x , called "V sub 
x". Information on this agent is limited. Based upon percutaneous liquid exposure, it 
appears to be less potent than VX. However, it is decidedly more potent than the G agents. 
It is also noted that it is more volatile than VX, so its potential airborne hazard is greater 
than that for VX. 10 See Table 11-17 (page 11-31) for toxicity estimates. 



11-29 



Table 11-16. Vx 



Alternate Designations: EA 1699; EDMM; Medemo 


Chemical Name: O-ethyl S-(2-dimethylaminoethyl) methylphosphonothiolate 


Synonyms: Phosphonothioic acid, methyl-, S-[2-(dimethylamino)ethyl] O-ethyl ester; 0-Aethyl-S-(2-dimethylaminoaethyl)- 
methylphosphonothioat (German); S-2- Dimethylaminoethyl-O-ethylester kyseliny methylthiofosfonove (Czech); O-Ethyl-S- 
(dimethylaminoethyl)-methylphosphonothioate 


CAS Registry No: 20820-80-8 


RTECS Number: 51366-09-7 


Physical and Chemical Properties 


Structural Formula: 

II / CH 3 

CH 3 CH 2 — 0— P— S— CH 2 CH 2 — N 

CH 3 NCH 3 

Molecular Formula: C 7 H 18 N0 2 PS 
Molecular Weight: 211.26 


Physical State 


Liquid 1 


Odor 


Odorless 2 


Boiling Point 


256°C (extrapolated) 3 ' 4 


FP/MP 


Data not available 


Liquid Density (g/mL) 


1 .060 @ 25°C; 1 .0820 @ 0°C (extrapolated) 1 


Vapor Density (relative to air) 


7.3 (calculated) 


Vapor Pressure (torr) 


6.73 x 10" 3 @ 25°C; 5.7 x 10" 4 @ 0°C (extrapolated) 3 ' 4 


Volatility (mg/m 3 ) 


7.64 x 10 1 @ 25°C; 7.02 @ 0°C (calculated from vapor pressure) 3 ' 4 


Latent Heat of Vaporization (kcal/mol) 


16.0 @ 25°C; 16.1 @ C C (calculated from vapor pressure) 3 ' 4 


Viscosity (cP) 


5.628 @ 25.0°C, 15.335 @ 0°C (extrapolated) 3 


Viscosity of Vapor (cP) 


5.56 x 1 0" 3 @ 25.0°C, 5.02 x 1 0" 3 @ 0°C 3 


Surface Tension (dynes/cm) 


31 .4 @ 25.0°C, 33.7 @ 0°C (extrapolated) 3 


Flash Point 


Data not available 


Decomposition Temperature 


Data not available 


Solubility 


Soluble in organic solvents; slightly soluble in water (source unidentified) 


Rate of Hydrolysis 


The rate coefficient for 7.8 x 10" 3 hr" 1 (based on a nonlinear least square fit) 5 


Hydrolysis Products 


Ethanol and the toxic product compound S-(2-dialkylamino-ethyl) 
methylphosphonothioic acid that is very stable in neutral water 


Stability in Storage 


Data not available 


Action on Metals or Other Materials 


Data not available 


Other Data 


Skin and eye toxicity 


Extremely toxic by skin and eye absorption 


Inhalation Toxicity 


Extremely potent 


Rate of action 


Rapid 8 


Means of detection 


M8 paper, M9 paper, M8A1, IPDS, CAM/ICAM, M18A2 CADK, MM1 7 


Protection required 


MOPP4; liquid nerve agents penetrate ordinary clothing rapidly 6 


Decontamination 


Flush eyes with water immediately. Use the M291 SDK to remove any liquid nerve 
agent on skin or clothing. Use the M295 IEDK for individual equipment. 5 STB, 
HTH, or household bleach is effective on equipment. Water, soaps, detergents, 
steam, and absorbents (earth, sawdust, ashes, and rags) are effective for physical 
removal. 10 


Use 


Quick-acting casualty agent 



11-30 



Table 11-16. Vx (Continued) 



NOTES 



Coulter, P.B., et al., Physical Constants of Thirteen V Agents (U), CWLR 2346, USA Chemical Warfare Laboratories, Army 

Chemical Center, MD, December 1959, UNCLASSIFIED Report (AD314520). 

2 TM 3-215/AFM, Military Chemistry and Chemical Agents, Washington DC, December 1963, UNCLASSIFIED Technical 

Manual (ADA 292141). 

3 Samuel, J.B., et al., Physical Properties of Standard Agents, Candidate Agents, and Related Compounds at Several 

Temperatures (U), ARCSL-SP-83015, June 1983, USA Armament Research and Development Command, Aberdeen 

Proving Ground, MD, UNCLASSIFIED Report (ADC033491). 

4 Newman, J.H., Edgewood Arsenal Notebook* NB 9298, p. 64 (U). 

5 Szafraniec, L.J., et al., On the Stoichiometry of Phosphonothiolate Ester Hydrolysis, CRDEC-TR-212, USA Chemical 

Research Developments Engineering Center, Aberdeen Proving Ground, MD, July 1990, UNCLASSIFIED Report 

(ADA225952). 

6 FM 8-285/NAVMED P-5041/AFJMAN 44-149/FMFM 11-11, Treatment of Chemical Agent Casualties and Conventional 

Military Chemical Injuries, 22 December 1995. 

7 Sharon Reutter, et al., Review and Recommendations for Human Toxicity Estimates for FM 3-1 1 .9, ECBC-TR-349, 

September 2003. 

s NIOSH-DOD-OSHA Sponsored Chemical and Biological Respiratory Protection Workshop Report, February 2000. 

9 DOD Chemical And Biological Defense Program Annual Report to Congress, Volume I, April 2003. 

10 FM 3-5/MCWP 3-37.3, NBC Decontamination, 28 July 2000. 



Table II-17. Vx Toxicity Estimates 



10 



Endpoint 


Toxicity 
(mg-min/m 3 ) 


MV(L) 


Exposure 
Duration 


ROE 


Probit 
Slope 


TLE 


ROD 


DOC 


N/A 


No toxicity estimates 
are recommended at 
this time because data 
are lacking. 


N/A 


N/A 


N/A 


N/A 


N/A 


Unknow 
n 


N/A 



6. Blood Agents 

Blood agents include AC, CK, and SA. The cyanogen blood agents AC and CK affect 
the bodily functions by inactivating the cytochrome oxidase system. 18 This poisoning 
prevents cell respiration and the normal transfer of oxygen from the blood to body tissues. 18 
SA causes hemolysis of the red blood cells. 19 Cyanogen agents are highly volatile and, 
therefore, nonpersistent. 20 Exposure at high concentrations causes effects within seconds 
and death within minutes in unprotected personnel. 18 The protective mask with fresh 
filters gives adequate protection against field concentrations. 1 After exposure to AC and 
CK, filters should be changed. 12 See FM 3-11.4 for filter change criteria. 

a. AC (see Table 11-18 [page 11-32]). Pure AC is a nonpersistent, colorless liquid 
that is highly volatile. It has a faint odor, similar to bitter almonds, that sometimes cannot 
be detected even in lethal concentrations. 12 Inhalation of small amounts causes giddiness, 
headache and faintness, confusion, palpitation and pain in the chest and region of the 
heart, difficulty breathing, and ultimately unconsciousness. 10 Inhalation of high 
concentrations can initially cause breathing that is deeper and more rapid than is normal 
at rest, followed closely by a loss of consciousness. This progresses to respiratory arrest, 
cessation of cardiac activity, and death. 18 Exposure to AC causes an increase in respiration 
within a few seconds; a casualty may not be able to hold his breath. The pink color of the 
casualty's skin suggests AC poisoning. 1 See Table 11-19 (page 11-33) for toxicity estimates. 



11-31 



Table 11-18. AC 



Alternate Designations: Cyclone (Russian); Cyclone B; Cyclon; Prussic acid, Forestite (French); Aero Liquid HCN 


Chemical Name: Hydrogen cyanide 


Synonyms: Hydrocyanic acid; Acide cyanhydrique (French); Acido cianidrico (Italian); Blausaeure (German); Blauwzuur 
(Dutch); Carbon hydride nitride (chn); Cyaanwaterstof (Dutch); Cyanwasserstoff (German); Cyjanowodor (Polish); Evercyn; 
Formic anammonide; Formonitrile 


CAS Registry Number: 74-90-8 


RTECS Number: MW6825000 


Physical and Chemical Properties 


Structural Formula: 




Molecular Formula: HCN 
Molecular Weight: 27.03 


H— C N 


Physical State 


Colorless liquid 1 


Odor 


Bitter almonds or peach kernels 2 ' 


Boiling Point 


25.5°C 4 < 1 


FP/BP 


-13.3°C(MP) 1 


Liquid Density (g/mL) 


0.6797 @ 25°C; 0.7162 @ 0°C 5 


Vapor Density (relative to air) 


0.93 (calculated) 


Vapor Pressure (torr) 


7.60 x 10 2 @ 25.5°C; 7.46 x 10 2 @ 25.0°C; 2.65 x 10 2 @ 0°C 4 ' 1 


Volatility (mg/m 3 ) 


1 . 1 x 1 6 @ 25.5°C; 1 .08 x 1 6 @ 25.0°C; 4.20 x 1 5 @ 0°C (calculated from vapor 
pressure) 4? 


Latent Heat of Vaporization 
(kcal/mol) 


6.72 @ 25.5°C; 6.72 @ 25.0°C; 6.71 @ 0°C (calculated from vapor pressure) 4 ' 1 


Viscosity (cP) 


Data not available 


Viscosity of Vapor (cP) 


Data not available 


Surface Tension (dynes/cm) 


Data not available 


Flash Point 


-18 C C (closed cup); 3 frequently ignites when explosively disseminated 6 


Decomposition Temperature 


Above 65.5 C C when stabilized; 6 forms explosive polymer on standing; 2 ' 3 stabilized 
material can be stored up to 65°C 6 


Solubility 


Miscible with water and common organic solvents including alcohol and ether 7 


Rate of Hydrolysis 


Slow under acidic conditions; rapid with traces of base or basic salts 8 


Hydrolysis Products 


Ammonia, formic acid (HCOOH), and amorphous brown solids 9 


Stability in Storage 


Pure AC is unstable in storage; forms explosive polymer on long standing; 2 ' 6 with 
the use of a stabilizer such as phosphoric acid, sulfur dioxide, or powdered copper, 
AC may be stored in metal containers for long periods of time @ temperatures up to 
65°C 2 ' 3 ' 6 


Action on Metals or Other Materials 


Corrodes iron, cast iron, chromium steel, and lead 2 


Other Data 


Skin and eye toxicity 


None 


Inhalation toxicity 


Can cause death within minutes. 10 


Rate of action 


Rapid 11 


Means of detection 


M256A1 CADK, M272 water testing kit, M18A2 CADK, 12 M18A3, MMI 


Protection required 


Protective mask with fresh filter; MOPP 4 when exposed to or handling liquid AC 13 


Decontamination 


Move to fresh air; none required under field conditions 14 


Use 


Quick-acting casualty agent 



II-32 



Table 11-18. AC (Continued) 



NOTES 



1 Giauque, W.F. and Ruehrwein, R.A., "The Entropy of Hydrogen Cyanide. Heat Capacity, Heat of Vaporization and Vapor 

Pressure. Hydrogen Bond Polymerization of the Gas in Chains of Indefinite Length." J. Am. Chem. Soc, Vol. 61, p. 2626, 

1939. 

2 Franke, S., Manual of Military Chemistry Volume I- Chemistry of Chemical Warfare Agents, ACSI-J-3890, Chemie der 

Kampfstoffe, East Berlin, April 1968, UNCLASSIFIED Report (AD849866). 

3 Lewis, R.J., Sax's Dangerous Properties of Industrial Materials, 10th ed., Vol. 3, p. 1992, John Wiley & Sons, Inc., New 

York, NY, 2001. 

4 Abercrombie, P., ECBC Notebook* NB 98-0079, p. 16 (U). 

5 Coates, J.E., and Davies, R.H., "Studies on Hydrogen Cyanide. Part XVIII. Some Physical Properties of Anhydrous 

Hydrogen Cyanide," J. Chem. Soc, p. 1194, 1950. 

6 W.R. Kirner, Summary Technical Report of Division 9, NDRC Volume 1, Chemical Warfare Agents, and Related Chemical 

Problems Part /-//, Chapter 2, p. 7, Office of Scientific Research and Development, Washington, DC, 1946, UNCLASSIFIED 

Report (AD234270). 

7 The Merck Index: An Encyclopedia of Chemicals, Drugs, and Biologicals, 1 3th ed., p. 857, Merck & Company, Inc., 

Whitehouse Station, NJ, 2001. 

8 Properties of War Gases Vol. II: Blood and Nettle Gases (U), ETF 1 00-41 A/ol-2, Chemical Corps Board, Army Chemical 

Center, Maryland, December 1956, CONFIDENTIAL Report (AD108457). 

9 Clark, D.N, Review of Reactions of Chemical Agents in Water, Final Report to USA Biomedical Research and Development 

Laboratory, Battelle, Columbus, OH, January 1989, UNCLASSIFIED Report (ADA213287). 

10 BG Russ Zajtchuk et al. (eds), Textbook of Military Medicine: Medical Aspects of Chemical and Biological Warfare, Office 

of the Surgeon General, 1997, Chap. 10, "Cyanide Poisoning." 

"NIOSH-DOD-OSHA Sponsored Chemical and Biological Respiratory Protection Workshop Report, February 2000. 

12 AFMAN 1 0-2602, Nuclear, Biological, Chemical, and Conventional (NBCC) Defense Operations and Standards 

(Operations), 29 May 2003. 

"FM 8-285/NAVMED P-5041/AFJMAN 44-149/FMFM 11-11, Treatment of Chemical Agent Casualties and Conventional 

Military Chemical Injuries, 22 December 1995. 

14 FM 8-9/NAVMED P-5059/AFJMAN 44-151, NATO Handbook on the Medical Aspects of NBC Defense Operations 

AMEDP-6(B), 1 February 1996. 



b. AC Toxicity Estimates (Table 11-19). Note that for an inhalation/ocular expouse 
the TLE is greater than 1. This means that the effective dosage increases with longer 
exposure durations and the concentration of the agent decreases. No toxicity effects for 
severe effects is recommended. The existing estimate is not supported by the available 
data. 



Table 11-19. AC Toxicity Estimates 



10 



Endpoint 


Toxicity 
(mg-min/m 3 ) 


MV(L) 


Exposure 
Duration 


ROE 


Probit 
Slope 


TLE 


ROD 


DOC 


Lethality 


LCt 50 : 2860 a 
(Provisional) 


15 


2 min 


Inhalation/ 
Ocular 


10 


1.85 b 


Some 


Low 


Severe effects 


ECt 50 : NR 


N/A 


N/A 


Inhalation/ 
Ocular 


Unknown 


Unknown 


Some 


N/A 


Threshold/odor 
(odor detection) 


EC 50 : 34 mg/m 3 c 


N/A 


Seconds 


Inhalation/ 
Ocular 


Unknown 


N/A 


N/A 


Low 


NOTES 


a Based on McNamara (1976). 

b See Appendix H for supporting toxicity profile estimates. 

c Based on TM 3-215 (1952) and secondary human data. 



c. CK (see Table 11-20 [page 11-34]). CK is a colorless gas with an irritating odor. 13 
It is nonpersistent and is used as a quick-acting casualty agent. 20 It is readily detectable by 
its immediate lacrimatory effect and its irritant effect on the nasal passage. 20 At high 
concentrations CK produces effects similar to AC. 10 However, in occasional instances, lung 
irritation can lead to pulmonary edema. 20 See Table 11-21 (page 11-35) for CK toxicity 
estimates. 



11-33 



Table 11-20. CK 



Alternate Designations: Mauguinite (French); CC; Klortsian 


Chemical Name: Cyanogen chloride 


Synonyms: Chlorcyan; Chlorine cyanide; Chlorocyan; Chlorocyanide; Chlorocyanogen; Chlorure de cyanogene (French) 


CAS Registry Number: 506-77-4 


RTECS Number: GT2275000 


Physical and Chemical Properties 


Structural Formula: 




Molecular Formula: CNCI 
Molecular Weight: 61.47 


CI C N 


Physical State 


Colorless gas 1 


Odor 


Lacrimatory and irritating 2 


Boiling Point 


1 2. 8°C (calculated) 35 


FP/MP 


-6.9°C (FP) 5 


Liquid Density (g/mL) 


1.202 @ 10°C; 1.222 @0°C 4 


Vapor Density (relative to air) 


2.1 (calculated) 


Vapor Pressure (torr) 


7.60 x 10 2 @ 12.8X; 6.80 x 10 2 @ 10°C; 4.48 x 10 2 @ 0°C 3 " 5 


Volatility (mg/m 3 ) 


2.62x10 6 @ 12.8°C;2.37x10 6 @ 10°C; 1.62 x 10 6 @ 0°C (calculated from vapor 
pressure) 3 " 5 


Latent Heat of Vaporization 
(kcal/mol) 


6.40 @ 12.8°C; 6.41 @ 10°C; 6.44 @ 0°C calculated from vapor pressure) 3 " 5 


Viscosity (cP) 


Data not available 


Viscosity of Vapor (cP) 


Data not available 


Surface Tension (dynes/cm) 


Data not available 


Flash Point 


Nonflammable 2 


Decomposition Temperature 


Approximately 149°C 6 


Solubility 


Solubility of liquefied CK in water is 71.4 g/L @ 20°C, 7 soluble in common organic 
solvents, sulfur mustard, and AC 1 


Rate of Hydrolysis 


The hydrolysis rate of CK with tap water is Ua = 180 hrs @ ambient temperature and 
pH7 8 


Hydrolysis Products 


Hydrogen chloride and cyanic acid (CNOH) 9 


Stability in Storage 


CK is stable in glass containers for long periods of time even @ elevated 
temperatures. Stable in steel containers for at least 1 year @ ambient temperature, 
but only about 9 weeks @ 60°C, after which time the gas begins to polymerize with 
formation of the corrosive solid, cyanuric chloride. Impurities have a tendency to 
promote explosive polymerization. 10,2 When stabilized using 5% anhydrous, 
powdered sodium pyrophosphate, munitions grade CK with a water content of less 
than 0.5% can be stored in most common metals for extended periods of time @ 
temperatures up to 100°C. 2 


Action on Metals or Other Materials 


None if CK is dry; slowly polymerizes when stored unstabilized in steel and other 
common metals @ elevated temperatures (see stability in storage section) 2 


Other Data 


Skin and eye toxicity 


Irritation to eyes similar to RCAs 


Inhalation toxicity 


Can cause death within minutes 11 


Rate of action 


Rapid 12 


Means of detection 


M256A1 CADK, M272 water testing kit, M18A2 CADK, M18A3 CADK, MMI 13 


Protection required 


Protective mask with fresh filters 14 


Decontamination 


Move to fresh air; none required under field conditions 15 


Use 


Quick-acting casualty agent 



II-34 



Table 11-20. CK (Continued) 



NOTES 



^ranke, S., Manual of Military Chemistry Volume I - Chemistry of Chemical Warfare Agents , ACSI-J-3890, Chemie der 

Kampfstoffe, East Berlin, April 1968, UNCLASSIFIED Report (AD849866). 

2 W.R. Kirner, Summary Technical Report of Division 9, NDRC Volume 1, Chemical Warfare Agents, and Related Chemical 

Problems Part l-ll, Chapter 2, Office of Scientific Research and Development, Washington, DC, 1946, UNCLASSIFIED 

Report (AD234270). 

3 Abercrombie, P., ECBC Notebook* NB 98-0079, p. 16 (U). 

4 Cook, R.P., and Robinson, P.L., "Certain Physical Properties of Cyanogen and its Halides," J. Chem. Soc, p. 1001, 1935. 

5 Douglas, D.E., and Winkler, C.A., "The Preparation, Purification, Physical Properties and Hydrolysis of Cyanogen Chloride," 

Ca. J. Research, Vol. 25B, p. 381, 1947. 

6 Brooks, Marguerite E, et al., Incineration/Pyrolysis of Several Agents and Related Chemical Materials Contained in 

Identification Sets, ARCSL-TR-79040, October 1979, UNCLASSIFIED Report (ADB042888). 

7 Carter, R.H., and Knight, H.C., Fundamental Study of Toxicity: Solubility of Certain Toxics in Water and in Olive Oil, EACD 

445, Chemical Warfare Service, Edgewood Arsenal, MD, May 1928, UNCLASSIFIED Report (ADB955216). 

8 Price, C.C., et al., "Hydrolysis and Chlorinolysis of Cyanogen Chloride", J. Amer. Chem. Soc, Vol. 69, p. 1640, 1947. 

9 Edwards, J.O., and Sauer, M., Chemical Reactivity of Cyanogen Chloride in Aqueous Solution, Quarterly Status Report 

(March through May 1972), Report No. Ill, DAAA15-71-C-0478-QSR 3, USA Chemical Laboratories, Edgewood Arsenal, 

MD, February 1973, UNCLASSIFIED Report (ADA090556). 

10 Henley, F.M., Surveillance Tests on 75 mm Steel Gas Shell Extending Over a Period of One Year, EACD 1 1 , Chemical 

Warfare Service, Edgewood Arsenal, MD, June 1920, UNCLASSIFIED Report (ADB959731). 

11 BG Russ Zajtchuk et al. (eds), Textbook of Military Medicine: Medical Aspects of Chemical and Biological Warfare, Office 

of the Surgeon General, 1997, Chap. 10, "Cyanide Poisoning." 

™NIOSH-DOD-OSHA Sponsored Chemical and Biological Respiratory Protection Workshop Report, February 2000. 

13 AFMAN 1 0-2602, Nuclear, Biological, Chemical, and Conventional (NBCC) Defense Operations and Standards 

(Operations), 29 May 2003. 

"FM 8-285/NAVMED P-5041/AFJMAN 44-149/FMFM 11-11, Treatment of Chemical Agent Casualties and Conventional 

Military Chemical Injuries, 22 December 1995. 

15 FM 8-9/NAVMED P-5059/AFJMAN 44-151, NATO Handbook on the Medical Aspects of NBC Defense Operations 

AMEDP-6(B), 1 February 1996. 



d. CK Toxicity Estimates (Table 11-21). Note that for an inhalation/ocular expouse 
the TLE is greater than 1. This means that the effective dosage increases with longer 
exposure durations and the concentration of the agent decreases. No toxicity estimates for 
lethal and severe effects are recommended. The existing estimates are not supported by 
the available data. 



Table 11-21. CK Toxicity Estimates 



10 



Endpoint 


Toxicity 
(mg-min/m 3 ) 


MV(L) 


Exposure 
Duration 


ROE 


Probit 
Slope 


TLE 


ROD 


DOC 


Lethality 


LCt 50 : NR 


N/A 


N/A 


Inhalation/ 
Ocular 


Unknown 


More than 1 


Probably 
Insignificant 


N/A 


Severe effects 


ECt 50 : NR 


N/A 


N/A 


Inhalation/ 
Ocular 


Unknown 


More than 1 


Probably 
Insignificant 


N/A 


Threshold 
(odor 
detection, 
tearing) 


EC 50 : 12mg/m 3a 


N/A 


Few 
Seconds 


Inhalation/ 
Ocular 


N/A 


N/A 


N/A 


Low 


NOTES 


a Based on human data and TM 3-215 (1952). 



e. SA (see Table 11-22 [page 11-36]). SA is a colorless gas with a disagreeable, 
garlic-like odor. 13 Symptoms from inhalation exposure include abdominal pain, confusion, 
dizziness, headache, nausea, shortness of breath, vomiting, and weakness. Severe exposure 
damages blood, causing anemia and kidney damage. 19 Exposure from liquid can cause 
frostbite. 19 See Table 11-23 (page 11-37) for toxicity estimates. 



11-35 



Table 11-22. SA 



Alternate Designations: Arthur 


Chemical Name: Arsenic trihydride 


Synonyms: Hydrogen arsenide, Arseniuretted hydrogen; Arsenic hydride; Arsenous hydride; Arsenowodor (Polish); 
Aresenwasserstoff (German) 


CAS Registry Number: 7784-42-1 


RTECS Number: CG6475000 


Physical and Chemical Properties 


Structural Formula: 

H— As— H 
I 
H 

Molecular Formula: AsH 3 
Molecular Weight: 77.95 


Physical State 


Colorless gas 1 


Odor 


Disagreeable, garlic-like 1 


Boiling Point 


-62.2°C (extrapolated) 2 


FP/MP 


-116°C(MP) 2 


Liquid Density (g/mL) 


1 .667 @ -75°C; 1 .734 @ -1 00°C 2 


Vapor Density (relative to air) 


2.7 (calculated) 


Vapor Pressure (torr) 


4.00 x 10 2 @ -75°C and 8.69 x 10 1 @ -100°C 2 


Volatility (mg/m 3 ) 


2.55 x 10 6 @ -75°C and 6.27 x 10 5 @ -100°C (calculated from vapor pressure) 2 


Latent Heat of Vaporization (kcal/mol) 


4.17 (calculated from Clausius Clapeyron equation which assumes constant heat 
of vaporization as a function of temperature) 2 


Viscosity (cP) 


Data not available 


Viscosity of Vapor (cP) 


Data not available 


Surface Tension (dynes/cm) 


Data not available 


Flash Point 


Flammable; forms explosive mixtures with air 3 


Decomposition Temperature 


300°C 1 


Solubility 


Solubility of SA in water is 0.028 g/100 g @ 20°C, 4 soluble in alkalis, halogen 
alkanes, hydrocarbons, and benzene 3 ' 


Rate of Hydrolysis 


Rapid in the presence of light. 1 Slow, in the absence of light and air @ 15.5°C and 
pH - 7; 32% of SA is hydrolyzed within 5 hrs and about 66% within 24 hrs 5 


Hydrolysis Products 


SA hydrolyzes to produce shiny black arsenic, which is also highly toxic 1 


Stability in Storage 


Unstable in most metal containers; metals catalyze decomposition; 6 on exposure 
to light, moist SA decomposes quickly, depositing shiny black arsenic 1 


Action on Metals or Other Materials 


Corrosive to most metals 6 


Other Data 


Skin and eye toxicity 


Exposure to liquid causes frostbite 7 


Inhalation toxicity 


Acute toxicity is high 7 


Rate of action 


1-24 hours (dependent on concentration and exposure duration) 7 


Means of detection 


MM1 


Protection required 


Protective mask with fresh filter; MOPP4 when exposed to or handling liquid SA 7 


Decontamination 


Move to fresh air; none required under field conditions 8 


Use 


Delayed-action casualty agent 



II-36 



Table 11-22. SA (Continued) 



NOTES 



''The Merck Index: An Encyclopedia of Chemicals, Drugs, and Biologicals, 13th ed., p. 138, Merck & Company, Inc., 

Whitehouse Station, NJ, 2001. 

2 Johnson, W. and Pechukas, A., "Hydrogen Compounds of Arsenic. I. Preparation of Arsine in Liquid Ammonia Some 

Physical Properties of Arsine," J. Am. Chem. Soc, Vol. 59, p. 2065, 1937. 

3 Franke, S., Manual of Chemistry Volume I- Chemistry of Chemical Warfare Agents, ACSI-J-3890, Chemie der Kampfstoffe, 

East Berlin, April 1968, UNCLASSIFIED Technical Manual (AD849866). 

4 Lewis, R.J., Sax's Dangerous Properties of Industrial Materials, 10th ed., Vol. 2, p. 309, John Wiley & Sons, Inc., New 

York, NY, 2001. 

5 Properties of War Gases Volume II: Blood and Nettle Gases (U), ETF 100-41/Vol-2, Chemical Corps Board, Army 

Chemical Center, Maryland, December 1956, CONFIDENTIAL Report (AD1 08457). 

6 TM 3-21 5/AFM 355-7, Military Chemistry and Chemical Agents, Departments of the Army and the Air Force, Washington 

DC, December 1963, UNCLASSIFIED Technical Manual (ADA292141). 

7 L. Fishbein and S. Czerczak, "Concise International Chemical Assessment Document 47: Arsine: Human Health Aspects," 

WHO, 2002. 

8 FM 8-9/NAVMED P-5059/AFJMAN 44-151 , NATO Handbook on the Medical Aspects of NBC Defense Operations 

AMEDP-6(B), 1 February 1996. 







Table II-23. SA Toxicity Estimates 


1U 








Endpoint 


Toxicity 
(mg-min/m 3 ) 


MV(L) 


Exposure 
Duration 


ROE 


Probit Slope 


TLE 


ROD 


DOC 


Lethality 


LCt 50 : 7500 a 
(Provisional) 


15 


2 min 


Inhalation/Ocular 


Not Calculated 


1.4 b 


Some 


Low 


NOTES 


a Based on modeling of 6 species. 

b See Appendix H for supporting toxicity profile estimates. 



7. Blister Agents (Vesicants) 

Blister agents are used to produce casualties, to degrade fighting efficiency, and to 
restrict use of terrain and equipment. 1 Blister agents are CW agents that act on the eyes, 
mucous membranes, lungs, skin, and blood-forming organs. 12 The most toxic route of 
exposure is inhalation/ocular. 10 The severity of a blister agent burn relates directly to the 
concentration of the agent, the duration of contact with the skin, 1 and the location on the 
body. Most blister agents are insidious in action except for lewisite (L) and phosgene oxime 
(CX), which cause immediate pain on contact. Assume MOPP4 whenever liquid or 
vaporized agents are known to be present. 1 Decontaminate within 1 or 2 minutes after 
exposure to help prevent or decrease tissue damage. 21 The blister agents are divided into 
three groups: mustards, arsenicals, and urticants. 

a. Mustards. This group of agents includes the sulfur mustards (H and HD) and 
the nitrogen mustards (HN-1, HN-2, and HN-3). Because of their physical properties, 
mustards are persistent under cool conditions; however, evaporation increases as the 
temperature increases. 21 It is possible to increase their persistency even more by 
dissolving them in thickeners. 12 

(1) Distilled Mustard (HD) (see Table 11-24 [page 11-38]). HD is a pale yellow 
to dark brown oily liquid with a garlic-like odor. 13 The eyes and respiratory tract are the 
most sensitive target organs. 10 The latency period for ocular effects is shorter than that for 
pulmonary effects, and acutely, ocular effects are more debilitating. 10 Both mustard vapor 
and liquid rapidly penetrate the skin. Warm, moist areas with thin skin (perineum, 
external genitalia, underarms, inside elbow, and neck) are much more sensitive. 21 Sweaty 
skin absorbs more mustard than dry skin. With an increase in temperature (>85 degrees F) 
and humidity, the effective dosages decrease and are about half of those for temperatures 
from 65 to 75 degrees F. 10 Mild symptoms caused from vapor exposure include tearing, 



11-37 



itchy, burning, gritty feeling in the eyes, rhinorrhea, sneezing, hoarseness, hacking cough, 
and erythema. Severe symptoms include marked lid edema, possible corneal damage, 
severe pain in the eyes, productive cough, dyspnea, and vesication. 21 Repeated exposures 
can cause an increase in sensitivity. 21 See Table 11-25 (page 11-40) for toxicity estimates. 

Table 11-24. HD 



Alternate Designations: EA 1033; HS; G.34; M.O; Kampstoff "Lost"; Mustard HD; Mustard gas; Mustard Sulfur; Mustard 
vapor; S-Lost; Schewefel-lost; S mustard; Sulfur mustard gas; Sulfur mustard; Sulphur mustard; Sulphur mustard gas; 
Yellow Cross liquid; Y; Yperite (French & German) 


Chemical Name: Bis (2-chloroethyl) sulfide 


Synonyms: 2, 2'-dichloroethyl sulfide; 1, 1'-Thiobis(2-chloroethane); B- B '-dichlorodiethyl sulphide; B ,B'- 
dichloroethylsulfide di - (2-chloro-ethyl) sulfide; Sulfide, bis (2-chloroethyl); Bis (beta-chloroethyl)sulfide; Bis (2- 
chloroethyljsulfide; Bis (2-chloroethyl) sulphide; 1-Chloro-2-(beta-chloroethylthio)ethane; 2,2'-Dichlorodiethyl sulfide; Di-2- 
chloroethyl sulfide; beta.beta'-Dichloroethyl sulfide; beta.beta-Dichlor-ethyl-sulphide; 2,2'-Dichloroethyl sulphide; Gelbkreuz 
(Czech); 1 , 1 '-Thiobis(2-chloroethane) 


CAS Registry Number: 505-60-2 


RTECS Number: WQ0900000 


Physical and Chemical Properties 


Structural Formula: 

CI-CH2-CH2-S-CH2-CH2-CI 
Molecular Formula: C 4 H 8 CI 2 S 
Molecular Weight: 159.07 


Physical State 


Pale yellow to dark brown oily liquid; 1 colorless when pure ' 


Odor 


Garlic-like 1,3 or horseradish 3 


Boiling Point 


218°C (extrapolated); at atmospheric pressure HD starts to decompose below the 
boiling point 


FP/MP 


14.45°C(FP) 2 


Solid Density (g/mL) 


1.372 @0°C; 1.333 @ 10°C 5 


Liquid Density (g/mL) 


1.2685 @25°C 6 


Vapor Density (relative to air) 


5.5 (calculated) 


Vapor Pressure (torr) 


1.06x10" 1 @25°C 4 


Volatility (mg/m 3 ) 


9.06 x 10 2 @ 25°C (calculated from vapor pressure) 4 


Latent Heat of Vaporization 
(kcal/mol) 


15.0 @ 25°C (calculated from vapor pressure) 4 


Viscosity (cP) 


3.951 @ 25.0°C, 7.746 @ 0°C (extrapolated) 7 


Viscosity of Vapor (cP) 


6.65 x 10" 3 @ 25.0°C, 6.00 x 10" 3 @ 0°C 7 


Surface Tension (dynes/cm) 


42.5 @ 25.0°C, 45.9 @ 0°C 7 


Flash Point 


105°C 5 


Decomposition Temperature 


180°C 8 


Solubility 


HD is practically insoluble in water; solubility of HD in distilled water is 0.92g 

HD/1 OOg solution at 22°C. HD is freely soluble in fats and oils, gasoline, kerosene, 

most organic solvents, and CW agents. 5 


Rate of Hydrolysis 


t-i/2 = 5 min @ 25°C via a S n 1 mechanism; 9 t-i/ 2 = 60 min @ 25°C in salt water. 10 
HD on or under water undergoes hydrolysis only if dissolved. The rate of HD 
hydrolysis is controlled by the rate of mass transfer and is very slow. 11 


Hydrolysis Products 


Hydrogen chloride, thiodiglycol, and sulfonium ion aggregates — one of which is also 
highly toxic 11 


Stability in Storage 


A small amount of degradation occurs when stored in steel ton containers for over 
50 years. 12 This degradation appears to be caused by the formation of solid 
deposits "heels" comprised of a six-membered ring cyclic sulfonium ion {1-(2- 
chloroethyl) -1,4-dithianium chloride}, HD, and Fe, which were detected at the 
bottom of the containers. 13 


Action on Metals or Other Materials 


Very little when pure. 3 The corrosion rate of HD on steel is 0.0001 inch/month @ 
65°C using munitions grade HD. 14 



II-38 



Table 11-24. HD (Continued) 



Other Data 



Skin and eye toxicity 



Eyes are very susceptible to low concentrations; incapacitating effects by skin 
absorption require higher concentrations. 15 



Inhalation toxicity 



Most toxic route of exposure 16 



Rate of action 



Delayed — hours to days 17 



Means of detection 



M8 paper, M9 paper, M256A1CADK, M90 AMAD, M21 ACAA, M22 ACADA, 
CAM/ICAM, M272 water testing kit, M18A3 CADK 18 , MM1, M18A2CADK 



Protection required 



MOPP4 whenever liquid or vaporized agents are present 15 



Decontamination 



Flush eyes with water immediately. Use the M291 SDK to remove any liquid nerve 
agent on skin or clothing. Use the M295 IEDK for individual equipment. 15 HTH or 
household bleach is effective on equipment. Water, soaps, detergents, steam, and 
absorbents (earth, sawdust, ashes, and rags) are effective for physical removal. 
STB does not effectively decontaminate mustard if it has solidified at low 
temperatures. 19 



Use 



Delayed-action casualty agent 



NOTES 

n Franke, S., Manual of Chemistry Volume l-Chemistry of Chemical Warfare Agents, ACSI-J-3890, Chemie der Kampfstoffe, 

East Berlin, April 1968, UNCLASSIFIED Technical Manual (AD849866). 

2 Felsing, W.A., et al., "The Melting Point of Mustard Gas," J. Amer.Chem. Soc, Vol. 70, p. 1966, 1948. 

3 Kibler, A.L., Data on Chemical Warfare, Technical Division Memorandum Report 456, Chemical Warfare Center, Edgewood 

Arsenal, MD, November 1942, UNCLASSIFIED Report (ADB969725). 

4 Penski, E.C., Properties of Di-(2-Chloroethyl) Sulfide I. Vapor Pressure Data Review and Analysis, ERDEC-TR-043, USA 

Edgewood Research, Development and Engineering Center, Aberdeen Proving Ground, MD, April 1993, UNCLASSIFIED 

Report (ADA 267059). 

5 Buckles, M.F., CW Vesicants: Selected Values for the Physical Properties of H, T, and Q (U), Special Report CRLR 542, 

Chemical Corps Chemical and Radiological Laboratories, Army chemical Center, MD, May 1956, UNCLASSIFIED Report 

(AD1 08272). 

6 Moelwyn-Hughes, E.A., and Owens, R., The Surface Tension, The Molecular Surface Energy and the Parachor of Toxic 

Compounds and of Certain Chlorides Used in Their Manufacture, Part XV of the Thermal Decomposition of the Secondary 

Alkylfluorophosphonites, Sutton Oak Report 544, Sutton Oak, England, September 1941, UNCLASSIFIED Report. 

7 Samuel, J.B., et al., Physical Properties of Standard Agents, Candidate Agents, and Related Compounds at Several 

Temperatures (U), ARCSL-SP-83015, USA Armament Research and Development Command, Aberdeen Proving Ground, 

MD, June 1983, UNCLASSIFIED Report (ADC033491). 

8 Williams, A.H., "The Thermal Decomposition of 2:2'-Dichlorodiethyl Sulphide,," J. Chem. Soc, p. 318, 1947. 

9 Bartlett, P.D., and Swain, C.G., "Kinetics of Hydrolysis and Displacement Reactions of B-B'-(Dichlorodiethyl Sulfide 

(Mustard Gas) and of B-Chloro-B'-hyroxidediethyl Sulfide (Mustard Chlorohydrin)," J. Chem. Soc, Vol. 71, p. 1406, 1949. 

lo Brookfield, K.J., et al., The Kinetics of the Hydrolysis of Vesicants Part ll-2:2'-Dichlorodiethylsulphide (H), SO/R/576, 

Military Intelligence Division, Great Britain, March 1942, UNCLASSIFIED Report. 

11 Yang, Y., et al., "Decontamination of Chemical Warfare Agents," Chem. Rev., Vol. 92, p. 1729, 1992. 

12 Abercrombie, P.L., and Butrow, A.B., Selected Physical Properties of Ton Container HD (Mustard) and VX, ERDEC-TR- 

450, USA Edgewood Research, Development, and Engineering Center, Aberdeen Proving Ground, MD, July 1998, 

UNCLASSIFIED Report (ADA350462). 

13 Yang, Y., et al., "Characterization of HD Heels and the Degradation of HD in Ton Containers," In Proceedings of the 1996 

ERDEC Scientifiec Conference on Chemical and Biological Defense Research 19-22 November 1996, UNCLASSIFIED 

Paper, ERDEC-SP-048, pp 353-360, USA Edgewood Research, Development and Engineering Center, Aberdeen Proving 

Ground, MD, October 1997, UNCLASSIFIED Report (ADA334105). 

14 Harris, B.L., et al., Corrosion by Vesicants: Rate of Corrosion of Steel and Other Metals by H, HQ, HN-3, HN-1 and L. 

Mostly at 65°C, Technical Division Memorandum Report 1031, USA Chemical Research and Development Laboratories, 

Army Chemical Center, MD, April 1945, UNCLASSIFIED Report (ADB963161). 

15 FM 8-285/NAVMED P-5041/AFJMAN 44-149/FMFM 11-11, Treatment of Chemical Agent Casualties and Conventional 

Military Chemical Injuries, 22 December 1995. 

16 Sharon Reutter, et al., Review and Recommendations for Human Toxicity Estimates for FM 3-11.9, ECBC-TR-349, 

September 2003. 

17 NIOSH-DOD-OSHA Sponsored Chemical and Biological Respiratory Protection Workshop Report, February 2000. 

18 DOD Chemical And Biological Defense Program Annual Report to Congress, Volume I, April 2003. 

19 FM 3-5/MCWP 3-37.3, NBC Decontamination, 28 July 2000. 



II-39 







Table 11-25. HD Toxicity Estimates 1 " 








Endpoint 


Toxicity 
(mg-min/m 3 ) 


MV(L) 


Exposure 
Duration 


ROE 


Probit 
Slope 


TLE 


ROD 


DOC 


Lethality 


LD 50 : 1400 mg a 


N/A 


N/A; 70-kg 
man 


Percutaneous 
Liquid b 


7 


N/A 


Little, if 
any 


Low 


LCt 50 : 1000 c 


15 


2 min 


Inhalation/ 
Ocular 


6 


1.5 d 


Some 


Low 


LCto 10,000 ae 


N/A 


30-360 min 


Percutaneous 
Vapor f 


7 


1 d.g 


Unknown 


Low h 


LCt 50 : 5000 lj 
(Provisional) 


N/A 


30-360 min 


Percutaneous 
Vapor ' 


7 


-| d,g 


Unknown 


Low 


Severe 
effects 
(vesication) 


ED 50 : 600 mg a 


N/A 


N/A; 
70-kg man 


Percutaneous 
Liquid b 


3 


N/A 


Little, if 
any 


Low 


ECt 50 : 500 ek 


N/A 


30-360 min 


Percutaneous 
Vapor ' 


3 


-| d,g,l 


Little, if 
any 


Moderate 


ECt 50 : 200 ik 


N/A 


30-360 min 


Percutaneous 
Vapor ' 


3 


1 d,g,l 


Little, if 
any 


Moderate h 


Severe 
effects (eyes) 


ECt 50 : 75 m 


N/A 


2-360 min 


Ocular 


3 


1 d 


Little, if 
any 


High 


Mild effects 
(erythema, 
itching, some 
pain) 


ECt 50 : 50 ae 


N/A 


30 min 


Percutaneous 
Vapor ' 


3 


1 d 


Little, if 
any 


Moderate 


ECt 50 : 25 a '' 


N/A 


30 min 


Percutaneous 
Vapor ' 


3 


1 d 


Little, if 
any 


Moderate 


Mild effects 
(eyes) 


ECt 50 : 25 a 


N/A 


2-360 min 


Ocular 


3 


1 d 


Some 


High 


Odor 
detection 


EC 50 : 0.6-1 mg/m 3n 


N/A 


Few 
seconds 


Inhalation 


N/A 


N/A 


Probably 
insignificant 


High 


NOTES 


a Based on Grotte and Yang (2001). 
b Bare skin. 

c Based on Grotte and Yang (2001) and Sommerville (2002). 
d See Appendix H for supporting toxicity profile estimates. 
9 Moderate temperatures (65-85°F). 

'Assumes personnel are masked with eye protection and clothed skin. 
g The TLE value is assumed to be 1 because the Ct profile is unknown. 
True human LCtso/ECtso values could be lower. 
'Hot temperatures (greater than 85°F). 

'Based on temperature factor given in Grotte and Yang (2001 ) and analysis of lethal data for GB percutaneous vapor 
exposure. 

k Based on Grotte and Yang (2001 ) and Letter (Dec 2001 ). 
'Based on human data. 
m Based on re-analysis of human data. 
"Based on primary human data. 



(2) Levinstein Mustard (H). Levinstein mustard is the original mustard (gas) 
of World War I vintage. It contains H and about 30 percent impurities. Properties of H are 
essentially the same as those for HD. The effective dosages of H and HD have been 
demonstrated to be quite comparable. 10 This manual does not differentiate between H and 
HD. 

(3) Nitrogen Mustard (HN-1) (see Table 11-26). HN-1 is a colorless liquid when 
pure with a faint, fishy or soapy odor. 13 It is used as a delayed-action casualty agent. The 
most prevalent symptoms in men inadvertently exposed to HN-1 vapor were conjunctivitis, 
laryngitis, bronchitis, hoarseness, coughing, elevated temperature, nausea, and vomiting. 
In this accidental exposure, the fact that these men, with all the knowledge available at 
their command as to precautions, protection against, and physical and chemical properties 



11-40 



of HN-1, were severely affected without knowledge of their exposure, serves to further 
emphasize the insidious nature of this agent. 10 See Table 11-27 (page 11-43) for HN-1 
toxicity estimates. 

Table 11-26. HN-1 



Alternate Designations: Ethyl S; NH-Lost; NOR nitrogen mustard; Nitrogen mustard gas-1; NSC 10873; TL 329; TL 1149 


Chemical Name: 2,2'-Dichlorotriethylamine 


Synonyms: Bis (2-chloroethyl)ethylamine; Ethylbis(2-chloroethyl)amine; N-ethyl, bis (B -chloroethyl)amine Ethylbis (beta- 
chloroethyl)amine 


CAS Registry Number: 538-07-8 


RTECS Number: YE1225000 


Physical and Chemical Properties 


Structural Formula: 

CH2CH2CI 

CH 3 CH 2 — N^ 

CH2CH2CI 

Molecular Formula: C 6 Hi3CI 2 N 
Molecular Weight: 170.08 


Physical State 


Dark oily liquid; 1 colorless when pure ■ 


Odor 


Faint, fishy or soapy 3 


Boiling Point 


192°C (extrapolated); 4,2 at atmospheric pressure HN-1 decomposes below the boiling 
point 5 


FP/MP 


-34.2°C(MP) 2 


Liquid Density (g/mL) 


1 .086 @ 25°C; 1 .1 10 @ 0°C (extrapolated) 2 


Vapor Density (relative to air) 


5.9 (calculated) 


Vapor Pressure (torr) 


2.44 x 10" 1 @ 25°C; 3.32 x 10" 2 @ 0°C (extrapolated) 4 ' 2 


Volatility (mg/m 3 ) 


2.23 x 10 3 @ 25°C; 3.31 x 10 2 @ 0°C (calculated from vapor pressure) 4 ' 2 


Latent Heat of Vaporization 
(kcal/mol) 


13.0 @ 25°C; 12.9 @ 0°C (calculated from vapor pressure) 4 ' 2 


Viscosity (cP) 


Data not available 


Viscosity of Vapor (cP) 


Data not available 


Surface Tension (dynes/cm) 


Data not available 


Flash Point 


Data not available; flashing has occurred on static detonation 3 


Decomposition Temperature 


For HN-1 • HCI, 12.7% is destroyed @ 149°C and @ 426°C >99% is destroyed. 5 


Solubility 


Solubility in water is approximately 4 g HN-1/L solution @ ambient temperature. 
Miscible with common organic solvents. 


Rate of Hydrolysis 


t-1/2 = 1 .3 min @ 25°C in aqueous solution 3 


Hydrolysis Products 


Complete hydrolysis yields the following: hydrochloric acid and ethyl diethanolamine, 
CH3CH2N(CH 2 CH 2 OH)2. 1 The process involves a complex series of reactions, with 
formation of the hydrochloride, cyclic imonium salts, a dimer, etc. 6 


Stability in Storage 


Polymerizes with the formation of solid deposits, when stored in steel containers; this 
amount is slight @ ambient temperature, but increases @ temperatures above 50°C. 


Action on Metals or Other Materials 


Corrosion of HN-1 on steel @ 65°C is 1 x 10" 5 to 5 x 10" 5 inch/month 8 


Other Data 


Skin and eye toxicity 


Eyes are very susceptible to low concentration; incapacitating effects by skin absorption 
require higher concentrations. 9 


Inhalation toxicity 


Most toxic route of exposure 10 


Rate of action 


Delayed: 12 hours or longer 11 


Means of detection 


M8 paper, M9 paper, M256A1 CADK, CAM/ICAM, MM1 12 


Protection required 


MOPP4 whenever liquid or vapor is present 9 



II-41 



Table 11-26. HN-1 (Continued) 



Decontamination 


Liquid on eyes and skin requires immediate decontamination. 9 HTH, household bleach 
is effective on equipment. Water, soaps, detergents, steam, and absorbents (earth, 
sawdust, ashes, and rags) are effective for physical removal. STB does not effectively 
decontaminate mustard if it has solidified at low temperatures. 13 


Use 


Delayed-action casualty agent 


NOTES 


1 Cheicante, R.L., et al., "Investigation for the Determination of Nitrogen Mustard and Related Compounds in Air by Gas 

Chromatography Using Solid Sorbent Collection and Thermal Desorption," In Proceedings of the 1998 ERDEC Scientific 

Conference on Chemical and Biological Defense Research 17-20 November 1998, UNCLASSFIED Paper (ADE491775), 

ERDEC-SP-004, pp 781-792, USA ECBC, Aberdeen Proving Ground, MD, July 1999, UNCLASSFIED Report (ADA375171). 

2 Dawson, T., A Memorandum Report New Compounds 2,2' Dichlorotriethylamine, Technical Division Memorandum Report 552, 

USA Chemical Research and Development Laboratories, Army Chemical Center, MD, February 1943, UNCLASSFIED Report 

(ADB960467). 

3 W.R. Kirner, Summary Technical Report of Division 9, NDRC Volume 1, Chemical Warfare Agents, and Related Chemical 

Problems Part /-//, Chapter 6, p. 59, Office of Scientific Research and Development, Washington, DC, 1946, UNCLASSIFIED 

Report (AD234270). 

4 Abercrombie, P., ECBC Notebook # NB 98-0079, p. 24 (U). 

5 Brooks, M. E. and Parker, G.A., et al., Incineration/Pyrolysis of Several Agents and Related Chemical Materials Contained in 

Identification Sets, ARCSL-TR-79040, October 1979, UNCLASSIFIED Report (ADB042888). 

6 W.R. Kirner, Summary Technical Report of Division 9, NDRC Volume 1, Chemical Warfare Agents, and Related Chemical 

Problems Part /-//, Chapter 19, p. 389, Office of Scientific Research and Development, Washington, DC, 1946, UNCLASSIFIED 

Report (AD234270). 

7 Harris, B.L., et al., Thickened Vesicants: Storage Stability of Unthickened and Thickened Nitrogen Mustards and Their Mixtures 

with Levinstein Mustard, Technical Division Memorandum Report 706, USA Chemical Research and Development 

Laboratories, Army Chemical Center, MD, July 1943, UNCLASSIFIED Report (ADB962153). 

8 Harris, B.L. andMacy, R., Corrosion by Vesicants: Rate of Corrosion of Steel and Other Metals by H, HQ, HN-3, HN-1, and L, 

Mostly at 65°C, Technical Division Memorandum Report 1031, USA Chemical Research and Development Laboratories, Army 

Chemical Center, MD, April 1945, UNCLASSIFIED Report (ADB963161). 

9 FM 8-285/NAVMED P-5041/AFJMAN 44-149/FMFM 11-11, Treatment of Chemical Agent Casualties and Conventional Military 

Chemical Injuries, 22 December 1995. 

10 Sharon Reutter, et al., Review and Recommendations for Human Toxicity Estimates for FM 3-11.9, ECBC-TR-349, 

September 2003. 

11 NIOSH-DOD-OSHA Sponsored Chemical and Biological Respiratory Protection Workshop Report, February 2000. 

12 DOD Chemical and Biological Defense Program Annual Report to Congress, Volume I, April 2003. 

13 FM 3-5/MCWP 3-37.3, NBC Decontamination, 28 July 2000. 



1 1 -42 



Table 11-27. HN-1 Toxicity Estimates 



10 



Endpoint 


Toxicity 
(mg-min/m 3 ) a 


MV(L) 


Exposure 
Duration 


ROE 


Probit 
Slope 


TLE 


ROD 


DOC 


Lethality 


LD 50 : 1400 mg 


N/A 


N/A; 70- 
kg man 


Percutaneous Liquid b 


Unknown 


N/A 


Unknown 


Low 


LCt 5 o: 1000 


15 


2 min 


Inhalation/Ocular 


Unknown 


a c,d 


Unknown 


Low 


LCt 50 : 10,000 e 


N/A 


30 min 


Percutaneous Vapor 


Unknown 


a c,d 


Unknown 


Low 


LCt 50 : 5000 9 


N/A 


30 min 


Percutaneous Vapor 


Unknown 


a c,d 


Unknown 


Low 


Severe 
effects 
(vesication) 


ED 50 : 600 mg 


N/A 


N/A; 70- 
kg man 


Percutaneous Liquid 


Unknown 


N/A 


Unknown 


Low 


ECt 50 : 500 e 


N/A 


30 min 


Percutaneous Vapor 


Unknown 


a c,d 


Unknown 


Low 


ECt 50 : 200 9 


N/A 


30 min 


Percutaneous Vapor 


Unknown 


a c,d 


Unknown 


Low 


Severe 
effects 
(eyes) 


ECt 5 : 75 


N/A 


2 min 


Ocular 


Unknown 


a c,d 


Unknown 


Low 


Mild effects 
(pain, 
erythema, 
itching) 


ECt 50 : 50 e 


N/A 


30 min 


Percutaneous Vapor 


Unknown 


a c,d 


Unknown 


Low 


ECt 50 : 25 9 


N/A 


30 min 


Percutaneous Vapor 


Unknown 


a c,d 


Unknown 


Low 


Mild effects 
(eyes) 


ECt 50 : 25 


N/A 


2 min 


Ocular 


Unknown 


a c,d 


Unknown 


Low 


NOTES 


a AII toxicity values given are provisional and based on recommendations for H/HD. 

b Bare skin. 

c See Appendix H for supporting toxicity profile estimate. 

d The TLE value is assumed to be 1 because the Ct profile is unknown. 

e Moderate temperatures (65-85°F). 

'Assumes personnel are masked with eye protection. 

9 Hot temperatures (greater than 85°F). 



(4) Nitrogen mustard (HN-2) (see Table 11-28). HN-2 is a colorless liquid when 
pure, and it has a fishy or soapy odor. 13 HN-2 is irritating to the eyes. 20 For other 
symptoms, see discussions of HN-1. See Table 11-29 (page 11-45) for HN-2 toxicity 
estimates. 

Table 11-28. HN-2 



Alternate Designations: Dichloren; N-methyl-Lost (German); Mustine; Mustargen; Mutagen; Nitrogen mustard; NSC 762; S; 
TL 146; T-1024; ENT-25294; MBA 



Chemical Name: Bis-(2-chloroethyl)methylamine 



Synonyms: 2,2'-Dichloro-N-methyldiethylamine; N, N-bis(2-chloroethyl)methylamine, N-methyl, bis((3 chloroethyl)amine; 
Bis(beta-chloroethyl)methylamine; Chloramine; Chlorethazine; Chlormethine; 2-Chloro-N-(2-chloroethyl)-N- 
methylethanamine; beta, beta'-Dichlorodiethyl-N-methylamine; 2,2'-Dichlorodiethyl-methylamine; Di(2- 
chloroethyl)methylamine; N,N-Di(chloroethyl)methylamine; Ethanamine, 2-chloro-N-(2-chloroethyl)-N-methyl-; 
Mechlorethamine; Mecloretamina (Italian); Methylbis(beta-chloroethyl)amine; Methylbis(2-chloroethyl)amine; N-Methyl-bis- 
chloraethylamin (German); N-Methyl-bis(beta-chloroethyl)amine; N-Methyl-bis(2-chloroethyl)amine; N-Methyl-2,2'- 
dichlorodiethylamine; Methyldi(2-chloroethyl)amine 



CAS Registry Number: 51-75-2 



RTECS Number: IA750000 



II-43 



Table 11-28. HN-2 (Continued) 



Physical and Chemical Properties 


Structural Formula: 

CH2CH2CI 

CH 3 — ISL 

Molecular Formula: C 5 HnCI 2 N CH CH CI 
Molecular Weight: 156.05 2 2 


Physical State 


Colorless liquid when pure 1 


Odor 


Fishy or soapy 2 


Boiling Point 


177°C (extrapolated); 3,2,4 at atmospheric pressure, HN-2 decomposes below its 
boiling point 5 


FP/MP 


-70°C(FP) 2 


Liquid Density (g/mL) 


1.1 18 @ 25°C; 1.1425 @ 0°C (extrapolated) 34 


Vapor Density (relative to air) 


5.4 (calculated) 


Vapor Pressure (torr) 


4.16 x 10" 1 @ 25°C; 5.70 x 10" 2 @ 0°C (extrapolated) 32,4 


Volatility (mg/m 3 ) 


3.49 x 10 3 @ 25°C; 5.22 x 10 2 @ 0°C (calculated from vapor pressure) 32,4 


Latent Heat of Vaporization 
(kcal/mol) 


12.9 @ 25°C; 12.8 @ 0°C (calculated from vapor pressure) 32,4 


Viscosity (cP) 


Data not available 


Viscosity of Vapor (cP) 


Data not available 


Surface Tension (dynes/cm) 


Data not available 


Flash Point 


Data not available 


Decomposition Temperature 


Decomposes before boiling point is reached; instability of HN-2 is associated with its 
tendency to polymerize or condense; the reactions involved could generate enough 
heat to cause an explosion. 5 


Solubility 


Solubility in water is approximately 13 g HN-2/L solution @ ambient temperature. 
Miscible with common organic solvents. 2 


Rate of Hydrolysis 


t-1/2 = 4 min @ 25°C in an aqueous solution. Slow except where alkali is present; 
dimerizes fairly rapidly in water. 2 


Hydrolysis Products 


The process involves a complex series of reactions, with formation of the 
hydrochloride, cyclic imonium salts, a dimer, etc. 6 


Stability in Storage 


Not stable; dimerizes on storage and deposits crystalline dimers 2 


Action on Metals or Other Materials 


None on steel and brass 2 


Other Data 


Skin and eye toxicity 


Eyes are very susceptible to low concentration; incapacitating effects by skin 
absorption require higher concentrations 7 


Inhalation toxicity 


Most toxic route of exposure 8 


Rate of action 


Delayed: 12 hrs or longer 9 


Means of detection 


M8 paper, M9 paper, M256A1 CADK, CAM/ICAM, MM1 10 


Protection required 


MOPP4 whenever liquid or vapor is present 7 


Decontamination 


Liquid on eyes and skin requires immediate decontamination. 7 HTH or household 
bleac
…[truncated]