The Neurotoxin Soman History
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Nerve Agent - Lntellipedia Page 1 Of9 Doc ID : 6637155 (U) Nerve Agent
This document is made available through the declassification efforts and research of John Greenewald, Jr., creator of: The Black Vault The Black Vault is the largest online Freedom of Information Act (FOIA) document clearinghouse in the world. The research efforts here are responsible for the declassification of MILLIONS of pages released by the U.S. Government & Military. Discover the Truth at: http://www.theblackvault.com Nerve Agent - lntellipedia Page 1 of9 Doc ID : 6637155 (U) Nerve Agent UNCLASSIFIED From lntellipedia Nerve Agents (also known as nerve gases, though these chemicals are liquid at room temperature) are a class of phosphorus-containing organic chemicals (organophosphates) that disrupt the mechanism by which nerves transfer messages to organs. The disruption is caused by blocking acetylcholinesterase, an enzyme that normally relaxes the activity of acetylcholine, a neurotransmitter. ...--------- --- -·---- - --- -·-- --- --- Contents • 1 Overview • 2 Biological Effects • 2.1 Mechanism of Action • 2.2 Antidotes • 3 Classes • 3.1 G-Series • 3.2 V-Series • 3.3 Novichok Agents • 3.4 Insecticides • 4 History • 4.1 The Discovery ofNerve Agents • 4.2 The Nazi Mass Production ofTabun • 4.3 Nerve Agents in Nazi Germany • 4.4 The Secret Gets Out • 4.5 Since World War II • 4.6 Ocean Disposal of Chemical Weapons • 5 Popular Culture • 6 References and External Links --------------- ----·-- - Overview As chemical weapons, they are classified as weapons of mass destruction by the United Nations according to UN Resolution 687, and their production and stockpiling was outlawed by the Chemical Weapons Convention of 1993; the Chemical Weapons Convention officially took effect on April 291997. Poisoning by a nerve agent leads to contraction of pupils, profuse salivation, convulsions, involuntary urination and defecation, and eventual death by asphyxiation as control is lost over respiratory muscles. -
Warning: the Following Lecture Contains Graphic Images
What the новичок (Novichok)? Why Chemical Warfare Agents Are More Relevant Than Ever Matt Sztajnkrycer, MD PHD Professor of Emergency Medicine, Mayo Clinic Medical Toxicologist, Minnesota Poison Control System Medical Director, RFD Chemical Assessment Team @NoobieMatt #ITLS2018 Disclosures In accordance with the Accreditation Council for Continuing Medical Education (ACCME) Standards, the American Nurses Credentialing Center’s Commission (ANCC) and the Commission on Accreditation for Pre-Hospital Continuing Education (CAPCE), states presenters must disclose the existence of significant financial interests in or relationships with manufacturers or commercial products that may have a direct interest in the subject matter of the presentation, and relationships with the commercial supporter of this CME activity. The presenter does not consider that it will influence their presentation. Dr. Sztajnkrycer does not have a significant financial relationship to report. Dr. Sztajnkrycer is on the Editorial Board of International Trauma Life Support. Specific CW Agents Classes of Chemical Agents: The Big 5 The “A” List Pulmonary Agents Phosgene Oxime, Chlorine Vesicants Mustard, Phosgene Blood Agents CN Nerve Agents G, V, Novel, T Incapacitating Agents Thinking Outside the Box - An Abbreviated List Ammonia Fluorine Chlorine Acrylonitrile Hydrogen Sulfide Phosphine Methyl Isocyanate Dibotane Hydrogen Selenide Allyl Alcohol Sulfur Dioxide TDI Acrolein Nitric Acid Arsine Hydrazine Compound 1080/1081 Nitrogen Dioxide Tetramine (TETS) Ethylene Oxide Chlorine Leaks Phosphine Chlorine Common Toxic Industrial Chemical (“TIC”). Why use it in war/terror? Chlorine Density of 3.21 g/L. Heavier than air (1.28 g/L) sinks. Concentrates in low-lying areas. Like basements and underground bunkers. Reacts with water: Hypochlorous acid (HClO) Hydrochloric acid (HCl). -
Organic & Biomolecular Chemistry
Organic & Biomolecular Chemistry Accepted Manuscript This is an Accepted Manuscript, which has been through the Royal Society of Chemistry peer review process and has been accepted for publication. Accepted Manuscripts are published online shortly after acceptance, before technical editing, formatting and proof reading. Using this free service, authors can make their results available to the community, in citable form, before we publish the edited article. We will replace this Accepted Manuscript with the edited and formatted Advance Article as soon as it is available. You can find more information about Accepted Manuscripts in the Information for Authors. Please note that technical editing may introduce minor changes to the text and/or graphics, which may alter content. The journal’s standard Terms & Conditions and the Ethical guidelines still apply. In no event shall the Royal Society of Chemistry be held responsible for any errors or omissions in this Accepted Manuscript or any consequences arising from the use of any information it contains. www.rsc.org/obc Page 1 of 7 Organic & Biomolecular Chemistry Journal Name RSCPublishing ARTICLE Selective chromo-fluorogenic detection of DFP (a Sarin and Soman mimic) and DCNP (a Tabun mimic) Cite this: DOI: 10.1039/x0xx00000x with a unique probe based on a boron dipyrromethene (BODIPY) dye Manuscript Received 00th January 2012, Accepted 00th January 2012 Andrea Barba-Bon,a,b Ana M. Costero,a,b* Salvador Gil,a,b Ramón Martínez- a,c,d a,c,d DOI: 10.1039/x0xx00000x Máñez, * and Félix Sancenón www.rsc.org/ A novel colorimetric probe (P4) for the selective differential detection of DFP (a Sarin and Soman mimic) and DCNP (a Tabun mimic) was prepared. -
The Assassination of Kim Jong Passing Himself Off As the Son of a Diplomat
Weekly Geopolitical Report By Bill O’Grady March 6, 2017 for his education. There he lived a low- profile existence learning languages and The Assassination of Kim Jong passing himself off as the son of a diplomat. Nam The young man showed an interest in technology while in Europe. On February 13th, Kim Jong Nam, the older half-brother of Kim Jong Un, the leader of At the age of 18, he was forced to return to the Democratic People’s Republic of Korea North Korea. He became close to his aunt, (DPRK), was assassinated at an airport in Kim Kyong Hui, Kim Jong Il’s sister, and Malaysia. This event offers insights into the uncle, the Dear Leader’s brother-in-law, “Hermit Kingdom” and shows the audacious Jang Song Thaek. Kim Jong Nam was nature of the regime. given government positions monitoring technology; reportedly, he was instrumental In this report, we begin with a biography of in creating North Korea’s intranet. King Jong Nam. Next, we will recap the assassination. The following section will Still, it became apparent that Kim Jong Il discuss the context of the murder, including had become jaded with his oldest son. China’s difficult relations with North Korea Instead, he lavished attention on his and potential rationale behind the youngest mistress, Ko Young Hee, another assassination. As always, we will conclude actress, and his youngest son, Kim Jong Un, with potential market ramifications. the “Young Marshall.” Who was Kim Jong Nam? As the oldest son faded from relevance, he Kim Jong Nam was born in 1971, the began to travel extensively, spending time in grandson of the “Great Leader,” Kim Il China and Southeast Asia. -
Chapter 6 PRETREATMENT for NERVE AGENT EXPOSURE
Pretreatment for Nerve Agent Exposure Chapter 6 PRETREATMENT FOR NERVE AGENT EXPOSURE MICHAEL A. DUNN, M.D., FACP*; BRENNIE E. HACKLEY, JR., PH.D.†; AND FREDERICK R. SIDELL, M.D.‡ INTRODUCTION AGING OF NERVE AGENT–BOUND ACETYLCHOLINESTERASE PYRIDOSTIGMINE, A PERIPHERALLY ACTING CARBAMATE COMPOUND Efficacy Safety Wartime Use Improved Delivery CENTRALLY ACTING NERVE AGENT PRETREATMENTS NEW DIRECTIONS: BIOTECHNOLOGICAL PRETREATMENTS SUMMARY *Colonel, Medical Corps, U.S. Army; Director, Clinical Consultation, Office of the Assistant Secretary of Defense (Health Affairs), Washing- ton, D.C. 20301-1200; formerly, Commander, U.S. Army Medical Research Institute of Chemical Defense, Aberdeen Proving Ground, Mary- land 21010-5425 †Scientific Advisor, U.S. Army Medical Research Institute of Chemical Defense, Aberdeen Proving Ground, Maryland 21010-5425 ‡Formerly, Chief, Chemical Casualty Care Office, and Director, Medical Management of Chemical Casualties Course, U.S. Army Medical Research Institute of Chemical Defense, Aberdeen Proving Ground, Maryland 21010-5425; currently, Chemical Casualty Consultant, 14 Brooks Road, Bel Air, Maryland 21014 181 Medical Aspects of Chemical and Biological Warfare INTRODUCTION Nerve agents are rapidly acting chemical com- cal as well and may impair physical and mental pounds that can cause respiratory arrest within performance. A pretreatment must be administered minutes of absorption. Their speed of action im- to an entire force under a nerve agent threat. Any poses a need for rapid and appropriate reaction by resulting performance decrement, even a compara- exposed soldiers, their buddies, or medics, who tively minor one, would make pretreatment use must administer antidotes quickly enough to save unacceptable in battlefield situations requiring lives. A medical defense against nerve agents that maximum alertness and performance for survival. -
Efficacy of the Repon1 Mutant IIG1 to Prevent Cyclosarin Toxicity in Vivo and to Detoxify Structurally Different Nerve Agents in Vitro
Arch Toxicol (2014) 88:1257–1266 DOI 10.1007/s00204-014-1204-z MOLECULAR TOXICOLOGY Efficacy of the rePON1 mutant IIG1 to prevent cyclosarin toxicity in vivo and to detoxify structurally different nerve agents in vitro Franz Worek · Thomas Seeger · Moshe Goldsmith · Yacov Ashani · Haim Leader · Joel S. Sussman · Dan Tawfik · Horst Thiermann · Timo Wille Received: 30 September 2013 / Accepted: 16 January 2014 / Published online: 30 January 2014 © Springer-Verlag Berlin Heidelberg 2014 Abstract The potent human toxicity of organophos- alkylmethylfluorophosphonates but had low efficiency with phorus (OP) nerve agents calls for the development of the phosphoramidate tabun and was virtually ineffective effective antidotes. Standard treatment for nerve agent with the nerve agent VX. This quantitative analysis vali- poisoning with atropine and an oxime has a limited effi- dated the model for predicting in vivo protection by cata- cacy. An alternative approach is the development of cata- lytic bioscavengers based on their catalytic efficiency, the lytic bioscavengers using OP-hydrolyzing enzymes such level of circulating enzyme, and the dose of the intoxicat- as paraoxonases (PON1). Recently, a chimeric PON1 ing nerve agent. The in vitro and in vivo results indicate mutant, IIG1, was engineered toward the hydrolysis of the that IIG1 may be considered as a promising candidate toxic isomers of soman and cyclosarin with high in vitro bioscavenger to protect against the toxic effects of a range catalytic efficiency. In order to investigate the suitabil- of highly toxic nerve agents. ity of IIG1 as a catalytic bioscavenger, an in vivo guinea pig model was established to determine the protective Keywords Nerve agents · Paraoxonase · Mutant · effect of IIG1 against the highly toxic nerve agent cyclo- Detoxification · Protection · Bioscavenger sarin. -
The Hyperspectral and Smartphone Technology in CBRNE Countermeasures and Defence JYVÄSKYLÄ STUDIES in COMPUTING 256
JYVÄSKYLÄ STUDIES IN COMPUTING 256 Jaana Kuula The Hyperspectral and Smartphone Technology in CBRNE Countermeasures and Defence JYVÄSKYLÄ STUDIES IN COMPUTING 256 Jaana Kuula The Hyperspectral and Smartphone Technology in CBRNE Countermeasures and Defence Esitetään Jyväskylän yliopiston informaatioteknologian tiedekunnan suostumuksella julkisesti tarkastettavaksi yliopiston Agora-rakennuksen auditoriossa 2 joulukuun 17. päivänä 2016 kello 12. Academic dissertation to be publicly discussed, by permission of the Faculty of Information Technology of the University of Jyväskylä, in building Agora, auditorium 2, on December 17, 2016 at 12 o’clock noon. UNIVERSITY OF JYVÄSKYLÄ JYVÄSKYLÄ 2016 The Hyperspectral and Smartphone Technology in CBRNE Countermeasures and Defence JYVÄSKYLÄ STUDIES IN COMPUTING 256 Jaana Kuula The Hyperspectral and Smartphone Technology in CBRNE Countermeasures and Defence UNIVERSITY OF JYVÄSKYLÄ JYVÄSKYLÄ 2016 Editors Timo Männikkö Department of Mathematical Information Technology, University of Jyväskylä Pekka Olsbo, Ville Korkiakangas Publishing Unit, University Library of Jyväskylä Produced in association with the National Defence University Department of Warfare URN:ISBN:978-951-39-6889-2 ISBN 978-951-39-6889-2 (PDF) ISBN 978-951-39-6888-5 (nid.) ISSN 1456-5390 Copyright © 2016, by University of Jyväskylä Jyväskylä University Printing House, Jyväskylä 2016 To my Mother Kirsti Kuula, born Huurtola (Haltt) * 23.1.1925 † 1.5.2013 ABSTRACT Kuula, Jaana The Hyperspectral and Smartphone Technology in CBRNE Countermeasures and Defence Jyväskylä: University of Jyväskylä, 2016, 214 p. (+ included articles) (Jyväskylä Studies in Computing ISSN 1456-5390; 256) ISBN 978-951-39-6888-5 (nid.) ISBN 978-951-39-6889-2 (PDF) Finnish summary Diss. Caused by industrial and military use as well as other sources of chemical, biological, radiological, nuclear and high-yield explosive (CBRNE) materials, the global threat of weapons of mass destruction (WMDs) remains in spite of such weapons being internationally prohibited. -
Soman (GD) Team (NRT) Quick Reference Guides (Qrgs) for Chemical Warfare Agents
NRT Quick Reference Guide: For references, please see Key References Cited/Used in National Response Soman (GD) Team (NRT) Quick Reference Guides (QRGs) for Chemical Warfare Agents. [January 2015 Update] QRGs are intended for Federal OSC/RPMs. Agent Classification: Schedule 1 Chemical Warfare Nerve Agent; CAS: 96-64-0; Formula: C7H16FO2P; Molecular Weight: 182.18 g/mol. Description: Colorless liquid that with aging may discolor to dark brown; generally odorless, but sometimes has odor of camphor or rotting fruit. GD is a lethal cholinesterase inhibitor with a mechanism of toxicity similar to organophosphate insecticides, though it is much more potent. GD is less volatile than Sarin (GB); it is much more volatile than persistent agents VX or Sulfur Mustard (HD). Environmental breakdown products of GD, including methylphosphonic acid (MPA), are relatively non-toxic. Other breakdown products include fluoride ion, which may exist as hydrofluoric acid (HF) depending on the pH. GD can react violently with bases, weak acids and strong oxidizers, and may decompose when in contact with metals, evolving flammable hydrogen gas. GD is combustible but not easily ignited when heated; GD vapors can form explosive mixtures with air. Persistence: GD is considered a “low persistent” chemical warfare agent. Vapor: minutes to hours; liquid: hours to days. Persistence will depend upon the amount and purity of the agent, method of release, environmental conditions, and types of surfaces and materials impacted. Porous, permeable, organic or polymeric materials such as carpets and vinyl tiles can accumulate agent by sorbing GD vapors and liquids, acting as “sinks,” thereby prolonging persistence. Physical properties are listed at/near STP unless otherwise indicated. -
Nerve Agents (Ga, Gb, Gd, Vx) Tabun (Ga) Cas # 77-81-6 Sarin (Gb) Cas # 107-44-8 Soman (Gd) Cas # 96-64-0 Vx Cas # 50782-69-9
NERVE AGENTS (GA, GB, GD, VX) TABUN (GA) CAS # 77-81-6 SARIN (GB) CAS # 107-44-8 SOMAN (GD) CAS # 96-64-0 VX CAS # 50782-69-9 Division of Toxicology ToxFAQsTM April 2002 This fact sheet answers the most frequently asked health questions (FAQs) about nerve agents. For more information, call the ATSDR Information Center at 1-888-422-8737. This fact sheet is one in a series of summaries about hazardous substances and their health effects. It is important you understand this information because this substance may harm you. The effects of exposure to any hazardous substance depend on the dose, the duration, how you are exposed, personal traits and habits, and whether other chemicals are present. HIGHLIGHTS: Exposure to nerve agents can occur due to accidental release from a military storage facility. Nerve agents are highly toxic regardless of the route of exposure. Exposure to nerve agents can cause tightness of the chest, excessive salivation, abdominal cramps, diarrhea, blurred vision, tremors, and death. Nerve agents (GA, GB, GD, VX) have been identified at 5 of the 1,585 National Priorities List sites identified by the Environmental Protection Agency (EPA). What are nerve agents GA, GB, GD, and VX? ‘ GA, GB, GD, and VX will be broken down in water quickly, but small amounts may evaporate. Nerve agents GA(tabun), GB (sarin), GD(soman), and VX are ‘ GA, GB, GD, and VX will be broken down in moist soil manufactured compounds. The G-type agents are clear, quickly. Small amounts may evaporate into air or travel colorless, tasteless liquids miscible in water and most below the soil surface and contaminate groundwater. -
Chapter 392 Ratification of Chemical Weapons
RATIFICATION OF CHEMICAL WEAPONS CONVENTION[CAP. 392. 1 CHAPTER 392 RATIFICATION OF CHEMICAL WEAPONS CONVENTION ACT NOTE FROM THE LAW COMMISSIONER: This Act was formally revoked by article 5 of Act V of 2000, however because of sub-article (2) of the same article, it is being reproduced in whole. To authorise the Government to ratify the Convention on the Prohibition of the Development, Production, Stockpiling and Use of Chemical Weapons and an their Destruction, to provide for the implementation by Malta of its provisions and for Malta’s membership of the Organisation for the Prohibition of Chemical Weapons, and for matters connected therewith or ancillary thereto. 28th April, 1997 ACT V of 1997, as amended by Legal Notice 216 of 2000. 1. The title of this Act is Ratification of Chemical Weapons Title. Convention Act. 2. (1) In this Act, unless the context otherwise requires - Interpretation. "Aircraft" has the same meaning which is given to it in the Civil Cap. 232. Aviation Act; "Convention" means the Convention on the Prohibition of the Development, Production, Stockpiling and Use of Chemical Weapons and on their Destruction, signed on behalf of Malta on the 13 January, 1993, in Paris, being a convention, a copy of the English text of which is set out in the Schedule to this Act; "Director" means the director of the National Authority for the purposes of this Act; "Director General" means the Director General of the Technical Secretariat; "Minister" means the Minister responsible for Foreign Affairs and Environment; "National Authority" -
Npr 4.3: Evidence Iraq Used Chemical Weapons During
Report: Iraq’s Use of CW in Gulf War EVIDENCE IRAQ USED CHEMICAL WEAPONS DURING THE 1991 PERSIAN GULF WAR by Jonathan B. Tucker Dr. Jonathan B. Tucker directs the Chemical and Biological Weapons Nonproliferation Project at the Center for Nonproliferation Studies, Monterey Institute of International Studies. Prior to this appointment, he worked at the U.S. Department of State, the Congressional Office of Technology Assessment, the Chemical and Biological Policy Division of the U.S. Arms Control and Disarmament Agency, and on the staff of the Presidential Advisory Committee on Gulf War Veterans’ Illnesses. He also served as a biological weapons inspector in Iraq with the United Nations Special Commission. id Iraqi forces employ chemical weapons dur- markable speed of the Coalition advance, combined with ing the 1991 Persian Gulf War? The U.S. De- the effectiveness of the strategic bombing campaign in Dpartment of Defense (DOD) and Central disrupting Iraq’s military command-and-control system, Intelligence Agency (CIA) have long insisted that they made it difficult for Iraqi commanders to select battle- did not. In a memorandum to Gulf War veterans dated field targets for chemical attack. Furthermore, the pre- May 25, 1994, Defense Secretary William J. Perry and vailing winds, which for six months had blown from the General John M. Shalikashvili, Chairman of the Joint northwest out of Iraq, shifted at the beginning of the Chiefs of Staff, declared, “There is no evidence, classi- ground war to the southeast, towards the Iraqi lines. fied -
Sarin - Wikipedia, the Free Encyclopedia Sarin from Wikipedia, the Free Encyclopedia
12/21/2015 Sarin - Wikipedia, the free encyclopedia Sarin From Wikipedia, the free encyclopedia Sarin, or GB, is a colorless, odorless Sarin[1] liquid,[5] used as a chemical weapon owing to its extreme potency as a nerve agent. It was classified as a weapon of mass destruction[6] in UN Resolution 687. Production and stockpiling of sarin was outlawed as of April 1997 by the Chemical Weapons Convention of 1993, and it is classified as a Schedule 1 substance. Sarin is an organophosphorus compound with the formula [(CH3)2CHO]CH3P(O)F. It can be lethal even at very low concentrations, with death following within 1 to 10 minutes after direct inhalation due to suffocation from lung muscle paralysis, unless some antidotes, Names typically atropine or biperiden and Preferred IUPAC name pralidoxime, are quickly (RS)-Propan-2-yl methylphosphonofluoridate administered.[5] People who absorb a Other names non-lethal dose, but do not receive immediate medical treatment, may (RS)-O-Isopropyl methylphosphonofluoridate; IMPF; suffer permanent neurological GB;[2] damage. 2-(Fluoro-methylphosphoryl)oxypropane; Phosphonofluoridic acid, P-methyl-, 1-methylethyl ester Contents Identifiers CAS Number 107-44-8 ChEBI 1 Production and structure CHEBI:75701 ChEMBL ChEMBL509554 2 Biological effects ChemSpider 7583 3 Degradation and shelf life Jmol interactive Image (http://chemapps.stolaf.edu/jmol/jmol.php? 3D model=FP%28%3DO%29%28OC%28C%29C%29C) 4 Effects and treatment PubChem 7871 4.1 Diagnostic tests UNII B4XG72QGFM 5 History InChI SMILES 5.1 Use as a weapon Properties