Safe Methods of Use 14: HSNO Class 6.1 Acutely Toxic Compounds
Total Page:16
File Type:pdf, Size:1020Kb
Load more
Recommended publications
-
Industry Compliance Programme
Global Chemical Industry Compliance Programme GC-ICP Chemical Weapons Convention December 2006 Version 1.0 GLOBAL CHEMICAL INDUSTRY COMPLIANCE PROGRAMME FOR IMPLEMENTING THE CHEMICAL WEAPONS CONVENTION The purpose of the handbook is to provide guidance to chemical facilities, traders and trading companies in developing a Global Chemical Industry Compliance Programme (GC-ICP) to comply with the Chemical Weapons Convention (CWC). The GC-ICP focuses first on determining if there is a reporting requirement to your National Authority and second on collecting the relevant support data used to complete the required reports. The GC-ICP is designed to provide a methodology to comply with the CWC and establish systems that facilitate and demonstrate such compliance. Each facility/company should also ensure that it follows its country’s CWC specific laws, regulations and reporting requirements. • Sections 2, 3, and 4 guide you through the process of determining if chemicals at your facility/ company should be reported to your National Authority for compliance with the CWC. • Section 5 provides recommended guidance on information that you may use to determine your reporting requirements under the CWC and administrative tools that your facility/company may use to ensure compliance with the CWC. • Section 6 provides a glossary of terms and associated acronyms. • Section 7 provides a listing of all National Authorities by country. CWC Global Chemical Industry Compliance Programme 1 TABLE OF CONTENTS Section 1 Overview What is the Chemical Weapons Convention? -
Copyrighted Material
1 Historical Milieu 1.1 Organophosphorus Nerve Agents 2 1.2 Blister Agents 5 1.3 Sternutator Agents 11 1.4 Chemical Weapons Convention (CWC) 13 1.4.1 Schedule of Chemicals 14 1.4.2 Destruction of Chemical Weapons 14 References 16 COPYRIGHTED MATERIAL Analysis of Chemical Warfare Degradation Products, First Edition. Karolin K. Kroening, Renee N. Easter, Douglas D. Richardson, Stuart A. Willison and Joseph A. Caruso. © 2011 John Wiley & Sons, Ltd. Published 2011 by John Wiley & Sons, Ltd. 2 ANALYSIS OF CHEMICAL WARFARE DEGRADATION PRODUCTS 1.1 ORGANOPHOSPHORUS NERVE AGENTS Organophosphorus (OP) type compounds, that is, deriva- tives containing the P=O moiety, were first discovered in the 1800s when researchers were investigating useful applica- tions for insecticides/rodenticides. There are many derivatives of organophosphorus compounds, however, the OP deriva- tives that are typically known as ‘nerve agents’ were discov- ered accidentally in Germany in 1936 by a research team led by Dr. Gerhard Schrader at IG Farben [1–4]. Schrader had noticed the effects and lethality of these organophosphorus compounds towards insects and began developing a new class of insecticides. While working towards the goal of an improved insecticide, Schrader experimented with numerous phosphorus-containing compounds, leading to the discovery of the first nerve agent, Tabun (or GA) (Figure 1.1). The potency of these insecticides towards humans was not realized until there was yet another accident, which involved a Tabun spill. Schrader and coworkers began experiencing symptoms, such as miosis (constriction of the pupils of the eyes), dizziness and severe shortness of breath, with numerous effects lasting several weeks [1, 4, 5]. -
Supplement to All Hazards Receipt Facility (AHRF) Screening Protocol
EPA/600/R-10/155 December 2010 Supplement to All Hazards Receipt Facility (AHRF) Screening Protocol SCIENCE Office of Research and Development National Homeland Security Research Center Supplement to All Hazards Receipt Facility (AHRF) Screening Protocol December 2010 Office of Research and Development National Homeland Security Research Center Acknowledgments This document is intended to be supplementary to the U.S. Environmental Protection Agency (EPA) and U.S. Department of Homeland Security (DHS) September 2008 All Hazards Receipt Facility Protocol (AHRF Protocol), and attempts to address considerations raised by stakeholders since publication of the protocol. Development of this document was funded by the U.S. Environmental Protection Agency (EPA) National Homeland Security Research Center (NHSRC), and includes information provided by EPA Regions 1, 6, and 10; EPA Office of Radiation and Indoor Air (ORIA), the Association of Public Health Laboratories (APHL): State Public Health Laboratories of Connecticut, Delaware, Massachusetts, Minnesota, New Jersey, New York, and Virginia; and New York City; and the Canadian Defence Research and Development Laboratory. This document was prepared by CSC under Contract EP-W-06- 046. Disclaimer This document is intended to be supplementary to the guidance provided in the U.S. Environmental Protection Agency (EPA) and U.S. Department of Homeland Security (DHS) September 2008 All Hazards Receipt Facility Protocol (AHRF Protocol), and attempts to address considerations raised by stakeholders since publication of the protocol. This supplement assumes that: • The September 2008 AHRF Protocol was developed and provided as a guide; implementation of the protocol and the screening equipment included in the protocol may vary among locations, depending on the goals and capabilities of the laboratory to which the facility is attached. -
Graphical Arrays of Chemical-Specific Health Effect Reference Values for Inhalation Exposures
EPA/600/R-09/061 Graphical Arrays of Chemical-Specific Health Effect Reference Values for Inhalation Exposures Includes Errata Sheet created on 4/6/2010 September 2009 U.S. Environmental Protection Agency Office of Research and Development National Center for Environmental Assessment Research Triangle Park, NC DISCLAIMER This document has been prepared by staff from the Hazardous Pollutant Assessment Group, National Center for Environmental Assessment, U.S. Environmental Protection Agency. Any opinions, findings, conclusions, or recommendations are those of the authors and do not necessarily reflect the views of the EPA. For questions concerning this document, please contact Dr. George Woodall (919-541-3896; [email protected]). September 2009 ii Errata Sheet Created 4/6/2010 for the document titled Graphical Arrays of Chemical-Specific Health Effect Reference Values for Inhalation Exposures, Final Table or Page Erratum Figure 133 Changed “values” to “value,” deleted “and OSHA,” and added “OSHA PEL” before “ACGIH ” in the first sentence of the second paragraph. Added the following sentence at the end of the second paragraph: “It should also be noted that the original documentaion for the OSHA PEL cited it as a Ceiling Value (OSHA, 1996, 192249) but OSHA later clarified in a memo that the value was a time-weighted average (OSHA, 1996, 598129)” Figure 133 Replaced Figure 2.15 2.15 Table 137 Replaced “OSHA-Ceiling” with “OSHA-PEL (TWA)” in the first 2.15 column of Table 2.15. Replaced “10 min” with “8 hr TWA” in the second column. Added reference in last column. 140 Added reference “OSHA (1996). -
Selected Analytical Methods for Environmental Remediation and Recovery (SAM) 2017
EPA/600/R-17/356 | September 2017 www.epa.gov/homeland-security-research Selected Analytical Methods for Environmental Remediation and Recovery (SAM) 2017 Office of Research and Development Homeland Security Research Program This page left intentionally blank EPA/600/R-17/356 | September 2017 Selected Analytical Methods for Environmental Remediation and Recovery (SAM) 2017 UNITED STATES ENVIRONMENTAL PROTECTION AGENCY Cincinnati, OH 45268 Office of Research and Development Homeland Security Research Program Disclaimer Disclaimer The U.S. Environmental Protection Agency (EPA) through its Office of Research and Development funded and managed the research described here under Contract EP-C-15-012 to CSRA Inc. This document is undergoing review and has not been approved for publication. The contents reflect the views of the contributors and technical work groups and do not necessarily reflect the views of the Agency. Mention of trade names or commercial products in this document or in the methods referenced in this document does not constitute endorsement or recommendation for use. Questions concerning this document or its application should be addressed to: Romy Campisano National Homeland Security Research Center Office of Research and Development (NG16) U.S. Environmental Protection Agency 26 West Martin Luther King Drive Cincinnati, OH 45268 (513) 569-7016 [email protected] Kathy Hall National Homeland Security Research Center Office of Research and Development (NG16) U.S. Environmental Protection Agency 26 West Martin Luther King -
Things to Be Done
DRAFT MAY 2003 ANNEX 1: CHEMICAL AGENTS 1. Introduction The large-scale use of toxic chemicals as weapons first became possible during the First World War (1914–1918) thanks to the growth of the chemical industry. More than 110 000 tonnes were disseminated over the battlefields, the greater part on the western front. Initially, the chemicals were used, not to cause casualties in the sense of putting enemy combatants out of action, but rather to harass. Though the sensory irritants used were powerful enough to disable those who were exposed to them, they served mainly to drive enemy combatants out of the trenches or other cover that protected them from conventional fire, or to disrupt enemy artillery or supplies. About 10% of the total tonnage of chemical warfare agents used during the war were chemicals of this type, namely lacrimators (tear gases), sternutators and vomiting agents. However, use of more lethal chemicals soon followed the introduction of disabling chemicals. In all, chemical agents caused some 1.3 million casualties, including 90 000 deaths. During the First World War, almost every known noxious chemical was screened for its potential as a weapon, and this process was repeated during the Second World War (1939–1945), when substantial stocks of chemical weapons were accumulated, although rarely used in military operations. Between the two world wars, a high proportion of all the new compounds that had been synthesized, or isolated from natural materials, were examined to determine their utility as lethal or disabling chemical weapons. After 1945, these systematic surveys continued, together with a search for novel agents based on advances in biochemistry, toxicology and pharmacology. -
Provisional Peer-Reviewed Toxicity Values for Lewisite (Casrn 541-25-3)
EPA/690/R-15/009F l Final 9-30-2015 Provisional Peer-Reviewed Toxicity Values for Lewisite (CASRN 541-25-3) Superfund Health Risk Technical Support Center National Center for Environmental Assessment Office of Research and Development U.S. Environmental Protection Agency Cincinnati, OH 45268 AUTHORS, CONTRIBUTORS, AND REVIEWERS CHEMICAL MANAGER Dan D. Petersen, PhD, DABT National Center for Environmental Assessment, Cincinnati, OH DRAFT DOCUMENT PREPARED BY SRC, Inc. 7502 Round Pond Road North Syracuse, NY 13212 PRIMARY INTERNAL REVIEWERS Jeffery Swartout, PhD, DABT National Center for Environmental Assessment, Cincinnati, OH This document was externally peer reviewed under contract to: Eastern Research Group, Inc. 110 Hartwell Avenue Lexington, MA 02421 3136 Questions regarding the contents of this document may be directed to the U.S. EPA Office of Research and Development’s National Center for Environmental Assessment, Superfund Health Risk Technical Support Center (513-569-7300). ii Lewisite TABLE OF CONTENTS COMMONLY USED ABBREVIATIONS AND ACRONYMS .................................................. iv BACKGROUND .............................................................................................................................1 DISCLAIMERS ...............................................................................................................................1 QUESTIONS REGARDING PPRTVs ............................................................................................1 INTRODUCTION ...........................................................................................................................2 -
CSAT Top-Screen Questions OMB PRA # 1670-0007 Expires: 5/31/2011
CSAT Top-Screen Questions January 2009 Version 2.8 CSAT Top-Screen Questions OMB PRA # 1670-0007 Expires: 5/31/2011 Change Log .........................................................................................................3 CVI Authorizing Statements...............................................................................4 General ................................................................................................................6 Facility Description.................................................................................................................... 7 Facility Regulatory Mandates ................................................................................................... 7 EPA RMP Facility Identifier....................................................................................................... 9 Refinery Capacity....................................................................................................................... 9 Refinery Market Share ............................................................................................................. 10 Airport Fuels Supplier ............................................................................................................. 11 Military Installation Supplier................................................................................................... 11 Liquefied Natural Gas (LNG) Capacity................................................................................... 12 Liquefied Natural Gas Exclusion -
Lewisite (L) 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 Lewisite (L) Team (NRT) Quick Reference Guides (QRGs) for Chemical Warfare Agents. [July 2015 Update] QRGs are intended for Federal OSC/RPMs. Agent Classification: Schedule 1 Chemical Warfare Blister (Vesicant) Agent; CAS: 541-25-3; Formula: C2H2AsCl3; Molecular Weight: 207.35 g/mol. Description: Lewisite is referred to as L-1 and is oily, colorless and odorless. When impure, it is a yellow brown through violet black liquid with a strong penetrating geranium odor. The manufacturing process affects physical properties, appearance, persistence, and analytical detection limits. Common impurities include two related compounds, lewisite 2 (L-2) and lewisite 3 (L-3). This QRG is based on L-1 but includes aspects of L-2 and L-3, and will use “L” as the collective abbreviation. L is a blister (vesicant) agent that produces immediate burning pain with blistering starting within a few hours. L is less volatile than Sarin (GB); it is much more volatile than persistent agents VX or HD. Environmental breakdown products of L are easily formed and include highly toxic arsenic (III) compounds, such as arsenites, lewisite oxide, and 2-chlorovinyl arsenous acid (CVAA); some cause similar blistering as L. Decontamination by-products of L include arsenic (V) compounds, which are generally less toxic than arsenic (III) compounds, but may be considered hazardous. Persistence: L is considered a “low to moderate persistent” chemical warfare agent. Vapor: minutes to hours; liquid: hours to days. Persistence will depend upon amount and purity of the agent, method of release, environmental conditions, and the types of surfaces and materials impacted. -
Field Screening Equipment Information Document, Companion
EPA/600/R-10/091 September 2010 Field Screening Equipment Information Document Companion to Standardized Analytical Methods for Environmental Restoration Following Homeland Security Events (SAM) - Revision 5.0 SCIENCOffice of Research and Development E National Homeland Security Research Center Field Screening Equipment Information Document Companion to Standardized Analytical Methods for Environmental Restoration Following Homeland Security Events (SAM) – Revision 5.0 UNITED STATES ENVIRONMENTAL PROTECTION AGENCY Office of Research and Development, National Homeland Security Research Center, Cincinnati, OH 45268 Office of Research and Development National Homeland Security Research Center, Threat and Consequence Assessment Division SAM Companion – Field Screening Equipment Document Acknowledgements This document was developed by the U.S. Environmental Protection Agency’s (EPA) National Homeland Security Research Center (NHSRC) within EPA’s Office of Research and Development as a companion to NHSRC’s Standardized Methods for Environmental Restoration Following Homeland Security Events (SAM). We wish to acknowledge the external peer reviews conducted by Matthew Arduino of the U.S. Centers for Disease Control and Prevention, Larry Burchfield of the Radiochemistry Society, Jordan Peccia of Yale University, and Fred Lee of G. Fred Lee & Associates, whose thoughtful comments contributed greatly to the quality of the information. The document was prepared by Computer Sciences Corporation (CSC) under EPA Contract No. EP-W-06-046. Disclaimer -
Safe Method of Use 11 HSNO Class 6.1 – Acutely Toxic Compounds
Safe Method of Use 11 HSNO Class 6.1 – Acutely Toxic Compounds HSNO Class 6.1 Toxic Compounds will cover a wide range of chemicals, for which an exhaustive list cannot be supplied. Always consult MSDS sheets prior to handling any chemical, observe precautions and follow the recommendations for their handling. The mandatory recommendations in the SMOU will apply to HSNO Class 6.1 A and B compounds and should be treated as recommendations for handling HSNO Class 6.1C compounds where this appropriate. MSDS databases (ChemWeb Gold and CCOHS) are available via the LEARN Database Appendix 1 provides a list (albeit not exhaustive) of HSNO 6.1 A, B and C Acutely Toxic Compounds with their classifications for your guidance. Please also note that chemicals that have primary HSNO classification of Class 3, 4, 5 or 8 may also be toxic. A. Incompatibilities • Care should be taken to keep HSNO Class 6.1A and B compounds well away from liquid acids, bases, strongly oxidising solutions and reactive compounds. B. Storage • Containers with toxic compounds with an oral LD50 less than 5 milligrams/kg (HSNO 6.1A), shall be clearly labelled with identity of compound and a warning indicating their toxicity. • If containers with HSNO 6.1 A toxic compounds that are liquids and are held in a refrigerator, these containers should be stored inside a separate secondary container (ie a plastic box) which has clear warnings of the toxic properties of its contents. Safe Method of Use 11 – HSNO Class 6.1 Version 4 Nov 2005 Page 1 of 9 • Laboratories with Toxic Compounds with an oral LD50 less than 5 milligrams/kg (HSNO 6.1A) in quantities capable of delivering a lethal dose shall be locked at the end of the working day or when no laboratory personnel are present. -
Chemicals Requiring EHS Pre-Approval
Chemicals Requiring EHS Approval Before Purchasing Chemical Name CAS # 1,3-Bis(2-chloroethylthio)-n-propane 63905-10-2 1,4-Bis(2-chloroethylthio)-n-butane 142868-93-7 1,5-Bis(2-chloroethylthio)-n-pentane 142868-94-8 1H-Tetrazole 288-94-8 2-chloroethyl ethylsulfide 693-07-2 2-Chloroethylchloro-methylsulfide 2625-76-5 2-Cyanoethyl diisopropylchlorophosphoramidite 89992-70-1 2-Ethoxyethanol 110-80-5 2-Ethoxyethylacetate 111-15-9 2-Methoxyethanol 109-86-4 2-Methoxyethylacetate 110-49-6 5-Nitrobenzotriazol 2338-12-7 Acetone cyanohydrin, stabilized 75-86-5 Acrolein 107-02-8 Acrylamide (powder) 79-06-1 Allylamine 107-11-9 Aluminum (powder) 7429-90-5 Aluminum phosphide 20859-73-8 Ammonia 7664-41-7 Ammonium nitrate 6484-52-2 Ammonium perchlorate 7790-98-9 Ammonium picrate 131-74-8 Arsenic 7440-38-2 Arsenic trichloride 7784-34-1 Arsenic trioxide 1327-53-3 Arsine 7784-42-1 Barium azide 18810-58-7 Beryllium 7440-41-7 Bis(2-chloroethylthio)methane 63869-13-6 Bis(2-chloroethylthiomethyl)ether 63918-90-1 Boron tribromide 10294-33-4 Boron trichloride 10294-34-5 Boron trifluoride 7637-07-2 Bromine 7726-95-6 Bromine chloride 13863-41-7 Bromine pentafluoride 7789-30-2 Bromine trifluoride 7787-71-5 Cadmium 7440-43-9 Calcium phosphide 1305-99-3 Carbon monoxide 630-08-0 Carbonyl fluoride 353-50-4 Carbonyl sulfide 463-58-1 Chlorine 7782-50-5 Chlorine dioxide 10049-04-4 Chlorine pentafluoride 13637-63-3 Chlorine trifluoride 7790-91-2 Chemicals Requiring EHS Approval Before Purchasing Chloroacetyl chloride 79-04-9 Chlorosarin 1445-76-7 Chlorosoman 7040-57-5 Chlorosulfonic