PAM 385-61. Toxic Chemical Agent Safety Standards
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Tremprime QD Low-Odor
Version: 1.1 Revision Date: 10/12/2018 SAFETY DATA SHEET 1. Identification Material name: TREMPRIME Q.D. LOW ODOR Material: 022045 805 Recommended use and restriction on use Recommended use : Coatings Restrictions on use: Not known. Manufacturer/Importer/Supplier/Distributor Information Tremco Canadian Sealants 220 Wicksteed Ave Toronto ON M4H 1G7 CA Contact person : EH&S Department Telephone : 1-800-263-6046 Emergency telephone number : 1-800-424-9300 (US); 1-613-996-6666 (Canada) 2. Hazard(s) identification Hazard Classification Physical Hazards Flammable liquids Category 3 Health Hazards Acute toxicity (Inhalation - vapor) Category 4 Serious Eye Damage/Eye Irritation Category 2A Germ Cell Mutagenicity Category 1B Carcinogenicity Category 1B Unknown toxicity - Health Acute toxicity, oral 40.8 % Acute toxicity, dermal 43 % Acute toxicity, inhalation, vapor 97 % Acute toxicity, inhalation, dust 100 % or mist Label Elements Hazard Symbol : 1/14 800000060000 Version: 1.1 Revision Date: 10/12/2018 Signal Word: Danger Hazard Statement: Flammable liquid and vapor. Harmful if inhaled. Causes serious eye irritation. May cause genetic defects. May cause cancer. Precautionary Statements Prevention: Keep away from heat, hot surfaces, sparks, open flames and other ignition sources. No smoking. Keep container tightly closed. Ground and bond container and receiving equipment. Use explosion-proof [electrical/ventilating/lighting/EF e:uipment. 5se non1sparking tools. Take action to prevent static discharges. Wear protective gloves/protective clothing/eye protection/face protection. Avoid breathing dust/fume/gas/mist/vapors/spray. 5se only outdoors or in a well1ventilated area. Wash thoroughly after handling. Obtain special instructions before use. Do not handle until all safety precautions have been read and understood. -
Decontamination of Agent Yellow, a Lewisite and Sulfur Mustard Mixture
EPA 600/R-14/436 | March 2015 | www.epa.gov/research Decontamination of Agent Yellow, a Lewisite and Sulfur Mustard Mixture Office of Research and Development National Homeland Security Research Center Decontamination of Agent Yellow, a Lewisite and Sulfur Mustard Mixture Evaluation Report National Homeland Security Research Center Office of Research and Development U.S. Environmental Protection Agency Research Triangle Park, NC 27711 ii Disclaimer The United States Environmental Protection Agency through its Office of Research and Development’s National Homeland Security Research Center funded and managed the research described here under EPA Contract Number EP-C-10-001, Work Assignment Number 4-28 with Battelle. This report has been peer and administratively reviewed and has been approved for publication as an Environmental Protection Agency report. It does not necessarily reflect views of the Environmental Protection Agency. No official endorsement should be inferred. The Environmental Protection Agency does not endorse the purchase or sale of any commercial products or services. Questions concerning this document or its application should be addressed to: Lukas Oudejans, Ph.D. Decontamination and Consequence Management Division National Homeland Security Research Center Office of Research and Development U.S. Environmental Protection Agency (MD-E343-06) 109 T.W. Alexander Drive Research Triangle Park, NC 27711 Phone: 919-541-2973 Fax: 919-541-0496 E-mail: [email protected] iii Acknowledgments The following individuals are acknowledged -
Warfare Agents for Modeling Airborne Dispersion in and Around Buildings
LBNL-45475 ERNEST ORLANDO LAWRENCE BERKELEY NATIn NAL LABORATORY Databaseof Physical,Chemicaland ToxicologicalPropertiesof Chemical and Biological(CB)WarfitreAgentsfor ModelingAirborneDispersionIn and AroundBuildings TracyThatcher,RichSextro,andDonErmak Environmental Energy Technologies Division DISCLAIMER This document was prepared as an account of work sponsored by the United States Government. While this document is believed to contain correct information, neither the United States Government nor any agency thereof, nor The Regents of the University of Catifomia, nor any of their employees, makes any warranty, express or implied, or assumes any legal responsibility for the accuracy, completeness, or usefulness of anY information, apparatus, product, or process disclosed, or represents that its use would not infringe privately owned rights. Reference herein to any specific commercial product, process, or service by its trade name, trademark, manufacturer, or otherwise, does not necessarily constitute or imply its endorsement, recommend at i on, or favoring by the United States Government or any agency thereof, or The Regents of the University of California. The views and opinions of authors expressed herein do not necessarily state or reflect those of the United States Government or any agency thereof, or The Regents of the University of California. Ernest Orlando Lawrence Berkeley National Laboratory is an equal opportunity employer. DISCLAIMER Portions of this document may be illegible in electronic image products. Images are produced -
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. -
Lewisite Fact Sheet
Lewisite Fact Sheet HIGHLIGHTS: It is unlikely that the general population will be exposed to blister agents Lewisite or Mustard-Lewisite. People who breathe in vapors of Lewisite or Mustard-Lewisite may experience damage to the respiratory system. Contact with the skin or eye can result in serious burns. Lewisite or Mustard-Lewisite also can cause damage to bone marrow and blood vessels. Exposure to high levels may be fatal. Blister agents Lewisite and Mustard-Lewisite have not been found in any of the 1,585 National Priorities List sites identified by the Environmental Protection Agency (EPA). What are lewisite and mustard-lewisite? Lewisite is an oily, colorless liquid with an odor like geraniums. Mustard-Lewisite Mixture is a liquid with a garlic-like odor. Mustard-Lewisite is a mixture of Lewisite and a sulfur mustard known as HD. Lewisite might have been used as a chemical weapon by Japan against Chinese forces in the 1930s, but such reports have not been confirmed. Any stored Lewisite in the United States must be destroyed before April 2007, as mandated by the Chemical Weapons Convention. What happens to lewisite and mustard-lewisite when it enters the environment? • Blister agents Lewisite and Mustard-Lewisite could enter the environment from an accidental release. • In air, blister agents Lewisite and Mustard-Lewisite will be broken down by compounds that are found in the air, but they may persist in air for a few days before being broken down. • Lewisite and Mustard-Lewisite will be broken down in water quickly, but small amounts may evaporate. • Lewisite and Mustard-Lewisite will be broken down in moist soil quickly, but small amounts may evaporate. -
Solubility and Solution-Phase Chemistry of Isocyanic Acid, Methyl Isocyanate, 2 and Cyanogen Halides 3 4 5 6 James M
Atmos. Chem. Phys. Discuss., https://doi.org/10.5194/acp-2018-1160 Manuscript under review for journal Atmos. Chem. Phys. Discussion started: 9 November 2018 c Author(s) 2018. CC BY 4.0 License. 1 Solubility and Solution-phase Chemistry of Isocyanic Acid, Methyl Isocyanate, 2 and Cyanogen Halides 3 4 5 6 James M. Roberts1, and Yong Liu2 7 8 1. NOAA/ESRL Chemical Sciences Division, Boulder, Colorado, 80305 9 2. Department of Chemistry, University of Colorado, Denver, Denver, Colorado, 80217 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 Atmos. Chem. Phys. Discuss., https://doi.org/10.5194/acp-2018-1160 Manuscript under review for journal Atmos. Chem. Phys. Discussion started: 9 November 2018 c Author(s) 2018. CC BY 4.0 License. 52 Abstract 53 54 Condensed phase uptake and reaction are important atmospheric removal processes for reduced nitrogen 55 species, isocyanic acid (HNCO), methyl isocyanate (CH3NCO) and cyanogen halides (XCN, X =Cl, Br, I), yet many 56 of the fundamental quantities that govern this chemistry have not been measured or are understudied. Solubilities 57 and first-order reaction rates of these species were measured for a variety of solutions using a bubble flow reactor 58 method with total reactive nitrogen (Nr) detection. The aqueous solubility of HNCO was measured as a function of 59 pH, and exhibited the classic behavior of a weak acid, with an intrinsic Henry’s law solubility of 20 (±2) M/atm, and -4 60 a Ka of 2.0 (±0.28) ×10 M (which corresponds to pKa = 3.7 ±0.06) at 298K. -
Hydroxyacetonitrile (HOCH2CN) As a Precursor for Formylcyanide (CHOCN), Ketenimine (CH2CNH), and Cyanogen (NCCN) in Astrophysical Conditions
A&A 549, A93 (2013) Astronomy DOI: 10.1051/0004-6361/201219779 & c ESO 2013 Astrophysics Hydroxyacetonitrile (HOCH2CN) as a precursor for formylcyanide (CHOCN), ketenimine (CH2CNH), and cyanogen (NCCN) in astrophysical conditions G. Danger1, F. Duvernay1, P. Theulé1, F. Borget1, J.-C. Guillemin2, and T. Chiavassa1 1 Aix-Marseille Univ, CNRS, PIIM UMR 7345, 13397 Marseille, France e-mail: [email protected] 2 Institut des Sciences Chimiques de Rennes, École Nationale Supérieure de Chimie de Rennes, CNRS, UMR 6226, Avenue du Général Leclerc, CS 50837, 35708 Rennes Cedex 7, France Received 8 June 2012 / Accepted 19 November 2012 ABSTRACT Context. The reactivity in astrophysical environments can be investigated in the laboratory through experimental simulations, which provide understanding of the formation of specific molecules detected in the solid phase or in the gas phase of these environments. In this context, the most complex molecules are generally suggested to form at the surface of interstellar grains and to be released into the gas phase through thermal or non-thermal desorption, where they can be detected through rotational spectroscopy. Here, we focus our experiments on the photochemistry of hydroxyacetonitrile (HOCH2CN), whose formation has been shown to compete with aminomethanol (NH2CH2OH), a glycine precursor, through the Strecker synthesis. Aims. We present the first experimental investigation of the ultraviolet (UV) photochemistry of hydroxyacetonitrile (HOCH2CN) as a pure solid or diluted in water ice. Methods. We used Fourier transform infrared (FT-IR) spectroscopy to characterize photoproducts of hydroxyacetonitrile (HOCH2CN) and to determine the different photodegradation pathways of this compound. To improve the photoproduct identifications, irradiations of hydroxyacetonitrile 14N and 15N isotopologues were performed, coupled with theoretical calculations. -
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). -
First Aid in the Prevention and Treatment of Chemical Casualties
OCD 2202-1 January 1943 FIRST AID in the Prevention and Treatment of CHEMICAL CASUALTIES Revised MEDICAL DIVISION OFFICE OF CIVILIAN DEFENSE Washington, D. C. PREFACE This booklet is intended for the personnel of Emergency Medical Field Units and others who may be immediately concerned in the cleansing of persons and the administration of first aid to chemical casualties. Identification, character- istics, and tactical uses of the various agents are discussed only briefly; the reader is referred to the Civilian Defense textbook, “Protection Against Gas,” for a more extensive discussion of these matters. For information on medical care and treatment consult Technical Manual 8-285, “Treat- ment of Casualties from Chemical Agents,” prepared by the War Department and published by the Government Printing Office. CONTENTS Chapter Page I. General Considerations 3 A. Kinds - 3 B. Recognition 3 1. Identification by Odor 4 2. Table of Odors and Effects 4 C. General Protective Measures 5 If. Lung irritants (Phosgene, Chlorpicrin, Chlorine, Nitric Fumes) 6 A. Latent Period 6 B. Effects 6 C. Symptoms 7 D. First Aid 7 Iff. Blister Bases (Mustard, Lewisite, Ethyldichlorar- sine) „ 8 A. Special Characteristics 8 Table of Differences between Lewisite and Mustard-_ 10 B. Mustard H 1. Effects-- 11 2. Prevention—First Aid . 12 C. Lewisite 14 1. Early Effects 15 2. Late Effects 15 3. Prevention—First Aid 15 D. Ethyldichlorarsine 16 1. Immediate Effects 16 2. First Aid 16 1 496407°—43 1 IV. Tear liases (Lacrimators) (Chloracetophenone, Chloracetophenone Solution, C N B Solution, Brom- benzyl cyanide) 17 A. Effects .1 ’ 17 B. -
A Thermophilic Bacterial Esterase for Scavenging Nerve Agents: a Kinetic, Biophysical and Structural Study
molecules Article A Thermophilic Bacterial Esterase for Scavenging Nerve Agents: A Kinetic, Biophysical and Structural Study Janek Bzdrenga , Elodie Trenet, Fabien Chantegreil , Kevin Bernal, Florian Nachon * and Xavier Brazzolotto Département de Toxicologie et Risques Chimiques, Institut de Recherche Biomédicale des Armées, 91220 Brétigny-sur-Orge, France; [email protected] (J.B.); [email protected] (E.T.); [email protected] (F.C.); [email protected] (K.B.); [email protected] (X.B.) * Correspondence: fl[email protected] Abstract: Organophosphorous nerve agents (OPNA) pose an actual and major threat for both military and civilians alike, as an upsurge in their use has been observed in the recent years. Currently available treatments mitigate the effect of the nerve agents, and could be vastly improved by means of scavengers of the nerve agents. Consequently, efforts have been made over the years into investigating enzymes, also known as bioscavengers, which have the potential either to trap or hydrolyze these toxic compounds. We investigated the previously described esterase 2 from Thermogutta terrifontis (TtEst2) as a potential bioscavenger of nerve agents. As such, we assessed its potential against G-agents (tabun, sarin, and cyclosarin), VX, as well as the pesticide paraoxon. We report that TtEst2 is a good bioscavenger of paraoxon and G-agents, but is rather slow at scav- enging VX. X-ray crystallography studies showed that TtEst2 forms an irreversible complex with the aforementioned agents, and allowed the identification of amino-acids, whose mutagenesis could lead to better scavenging properties for VX. In conjunction with its cheap production and purification Citation: Bzdrenga, J.; Trenet, E.; processes, as well as a robust structural backbone, further engineering of TtEst2 could lead to a Chantegreil, F.; Bernal, K.; Nachon, F.; stopgap bioscavenger useful for in corpo scavenging or skin decontamination. -
Chapter 4: HAZARD COMMUNICATION
Chapter 4: HAZARD COMMUNICATION The text of this chapter represents the agreement reached on a harmonised hazard communication system as part of the work on the GHS, with minor editorial changes. Additional explanatory text has been added in some sections in order to provide guidance for the reader on how to interpret the GHS agreed text. Where this is the case, the text is italicised and placed in a box to differentiate it from the agreed GHS text. OBJECTIVES AND SCOPE 1. One of the objective of the work on the GHS has been the development of a harmonised hazard communication system including labelling, safety data sheets and easily understandable symbols, based on the classification criteria developed by the focal points within the IOMC Co-ordinating Group for the Harmonisation of Chemical Classifications Systems, CG/HCCS. This work has been carried out under the auspices of the ILO, by the ILO Working Group on Hazard Communication. The specific Terms of Reference and Membership of the Working Group are provided in Annex 1. In addition the principles contained in the IOMC CG/HCCS Terms of Reference and the document “Description and Further Clarification of the Anticipated Application of the GHS (also referred to as “The Scope Document”) also applied to the work on harmonisation of hazard communication (see Chapter 2). Application of the Harmonised Hazard Communication System 2.The harmonised system for hazard communication includes the appropriate labelling tools to convey information about each of the hazard classes and categories in the GHS. The use of symbols, signal words or hazard statements other than those which have been assigned to each of the GHS hazard classes and categories would be contrary to harmonisation. -
Hazcom Training Requirements Due Dec. 1, 2013
This presentation reviews the new chemical container labeling and safety data sheet requirements under the new Hazard Communication standard. Reference information about the labeling and safety data sheet format can be found on www.osha.gov; specifically on the hazard communication Web page at www.osha.gov/dsg/hazcom. 1 (Read slide) The GHS manual that is accessed from the website provides additional detail about the system for chemical classifications and hazard communication. The purpose of the new HazCom standard is to ensure the hazards of all chemicals produced or imported are classified and information concerning the classified hazards is transmitted to employers and employees in a more informative and consistent manner based on the criteria established in the GHS. 2 The globally harmonized system is a…(read 1st two paragraphs on slide) The GHS is the culmination of more than a decade of work. There were many individuals involved from a multitude of countries, international organizations, and stakeholder organizations. There work spanned a wide range of expertise, from toxicology to fire protection, and ultimately required extensive good will and the willingness to compromise, in order to achieve a system that provides a single, globally harmonized system, to address classification of hazardous substances and mixtures, and the communication of these hazards through revised labeling and SDS’s. The new system is being implemented throughout the world by countries including Canada, the European Union, China, Australia, and Japan. Other U.S. Agencies including the Department of Transportation (DOT), Environmental Protection Agency, and the Consumer Product Safety Commission actively participated in developing the GHS.