Material Safety Data Sheets and Their Relevance to Customs Work
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Chemistry Lab Hygiene Plan
UNIVERSITY OF MAINE Department of Chemistry CHEMICAL HYGIENE PLAN October, 2001 Contents I. Personal Protective Equipment .. 3 II. Storage of Chemicals .. 6 III. Disposal of Chemicals .. 16 IV. Reading MSDS .. 19 V. Emergencies and the Emergency Action Plan .. 26 VI. Standard Operating Guidelines .. 33 VII. General Housekeeping and Prudent Practices .. 40 2 I. Laboratory Clothing and Personal Protective Equipment A. Dressing for safety in the laboratory Individuals should prepare for a safe laboratory experience by dressing appropriately for laboratory work. Appropriate clothing includes the following: • Shoes should fully cover the feet to protect against spills; no open-toed shoes or sandals are permitted, and shoes with mesh inserts (such as athletic shoes) are not recommended. One may choose to keep a pair of sturdy leather shoes in the laboratory to change into upon arrival. • Trousers or skirts falling below the knee are preferred; if shorter garments are worn, a lab coat or apron of below knee length is required. Preferred materials are resistant polyester, cotton or wool, since ordinary polyester and acrylics may be dissolved by common laboratory solvents. • Neckties, if worn, should be firmly clipped to the shirt or confined inside a lab coat or apron. • Loose, flowing garments and scarves should be avoided; they may easily pick up spills or trail through a burner flame. • In a laboratory where open flames may be used, long hair should be confined. • Loose jewelry should be avoided, since it may catch on equipment. Also avoid ornate rings that can damage protective gloves or make wearing or removing gloves difficult B. Protective Equipment Every laboratory must have available, and workers must be trained in the use of, safety goggles, face masks, lab coats or aprons, gloves, and reaction shields. -
Transport of Dangerous Goods
ST/SG/AC.10/1/Rev.16 (Vol.I) Recommendations on the TRANSPORT OF DANGEROUS GOODS Model Regulations Volume I Sixteenth revised edition UNITED NATIONS New York and Geneva, 2009 NOTE The designations employed and the presentation of the material in this publication do not imply the expression of any opinion whatsoever on the part of the Secretariat of the United Nations concerning the legal status of any country, territory, city or area, or of its authorities, or concerning the delimitation of its frontiers or boundaries. ST/SG/AC.10/1/Rev.16 (Vol.I) Copyright © United Nations, 2009 All rights reserved. No part of this publication may, for sales purposes, be reproduced, stored in a retrieval system or transmitted in any form or by any means, electronic, electrostatic, magnetic tape, mechanical, photocopying or otherwise, without prior permission in writing from the United Nations. UNITED NATIONS Sales No. E.09.VIII.2 ISBN 978-92-1-139136-7 (complete set of two volumes) ISSN 1014-5753 Volumes I and II not to be sold separately FOREWORD The Recommendations on the Transport of Dangerous Goods are addressed to governments and to the international organizations concerned with safety in the transport of dangerous goods. The first version, prepared by the United Nations Economic and Social Council's Committee of Experts on the Transport of Dangerous Goods, was published in 1956 (ST/ECA/43-E/CN.2/170). In response to developments in technology and the changing needs of users, they have been regularly amended and updated at succeeding sessions of the Committee of Experts pursuant to Resolution 645 G (XXIII) of 26 April 1957 of the Economic and Social Council and subsequent resolutions. -
Reactions of Lithium Nitride with Some Unsaturated Organic Compounds. Perry S
Louisiana State University LSU Digital Commons LSU Historical Dissertations and Theses Graduate School 1963 Reactions of Lithium Nitride With Some Unsaturated Organic Compounds. Perry S. Mason Jr Louisiana State University and Agricultural & Mechanical College Follow this and additional works at: https://digitalcommons.lsu.edu/gradschool_disstheses Recommended Citation Mason, Perry S. Jr, "Reactions of Lithium Nitride With Some Unsaturated Organic Compounds." (1963). LSU Historical Dissertations and Theses. 898. https://digitalcommons.lsu.edu/gradschool_disstheses/898 This Dissertation is brought to you for free and open access by the Graduate School at LSU Digital Commons. It has been accepted for inclusion in LSU Historical Dissertations and Theses by an authorized administrator of LSU Digital Commons. For more information, please contact [email protected]. This dissertation has been 64—5058 microfilmed exactly as received MASON, Jr., Perry S., 1938- REACTIONS OF LITHIUM NITRIDE WITH SOME UNSATURATED ORGANIC COMPOUNDS. Louisiana State University, Ph.D., 1963 Chemistry, organic University Microfilms, Inc., Ann Arbor, Michigan Reproduced with permission of the copyright owner. Further reproduction prohibited without permission. Reproduced with permission of the copyright owner. Further reproduction prohibited without permission. Reproduced with permission of the copyright owner. Further reproduction prohibited without permission. REACTIONS OF LITHIUM NITRIDE WITH SOME UNSATURATED ORGANIC COMPOUNDS A Dissertation Submitted to the Graduate Faculty of the Louisiana State University and Agricultural and Mechanical College in partial fulfillment of the requireiaents for the degree of Doctor of Philosophy in The Department of Chemistry by Perry S. Mason, Jr. B. S., Harding College, 1959 August, 1963 Reproduced with permission of the copyright owner. Further reproduction prohibited without permission. -
Notable Reactivity of Acetonitrile Towards Li2o2/Lio2 Probed By
Topics in Catalysis https://doi.org/10.1007/s11244-018-1072-5 ORIGINAL ARTICLE Notable Reactivity of Acetonitrile Towards Li2O2/LiO2 Probed by NAP XPS During Li–O2 Battery Discharge Tatiana K. Zakharchenko1 · Alina I. Belova1 · Alexander S. Frolov1 · Olesya O. Kapitanova1 · Juan‑Jesus Velasco‑Velez2 · Axel Knop‑Gericke2,5 · Denis Vyalikh3,4 · Daniil M. Itkis1 · Lada V. Yashina1 © Springer Science+Business Media, LLC, part of Springer Nature 2018 Abstract One of the key factors responsible for the poor cycleability of Li–O2 batteries is a formation of byproducts from irreversible reactions between electrolyte and discharge product Li 2O2 and/or intermediate LiO2. Among many solvents that are used as electrolyte component for Li–O2 batteries, acetonitrile (MeCN) is believed to be relatively stable towards oxidation. Using near ambient pressure X-ray photoemission spectroscopy (NAP XPS), we characterized the reactivity of MeCN in the Li–O2 battery. For this purpose, we designed the model electrochemical cell assembled with solid electrolyte. We discharged it first in O2 and then exposed to MeCN vapor. Further, the discharge was carried out in O2 + MeCN mixture. We have dem- onstrated that being in contact with Li–O2 discharge products, MeCN oxidizes. This yields species that are weakly bonded to the surface and can be easily desorbed. That’s why they cannot be detected by the conventional XPS. Our results suggest that the respective chemical process most probably does not give rise to electrode passivation but can decrease considerably the Coulombic efficiency of the battery. Keywords Li–O2 battery · In situ NAP XPS · Acetonitrile · Side reactions 1 Introduction Li–O2 batteries promise extraordinary high specific energy that makes them interesting for the next generation power technologies [1, 2]. -
Chemical Chemical Hazard and Compatibility Information
Chemical Chemical Hazard and Compatibility Information Acetic Acid HAZARDS & STORAGE: Corrosive and combustible liquid. Serious health hazard. Reacts with oxidizing and alkali materials. Keep above freezing point (62 degrees F) to avoid rupture of carboys and glass containers.. INCOMPATIBILITIES: 2-amino-ethanol, Acetaldehyde, Acetic anhydride, Acids, Alcohol, Amines, 2-Amino-ethanol, Ammonia, Ammonium nitrate, 5-Azidotetrazole, Bases, Bromine pentafluoride, Caustics (strong), Chlorosulfonic acid, Chromic Acid, Chromium trioxide, Chlorine trifluoride, Ethylene imine, Ethylene glycol, Ethylene diamine, Hydrogen cyanide, Hydrogen peroxide, Hydrogen sulfide, Hydroxyl compounds, Ketones, Nitric Acid, Oleum, Oxidizers (strong), P(OCN)3, Perchloric acid, Permanganates, Peroxides, Phenols, Phosphorus isocyanate, Phosphorus trichloride, Potassium hydroxide, Potassium permanganate, Potassium-tert-butoxide, Sodium hydroxide, Sodium peroxide, Sulfuric acid, n-Xylene. Acetone HAZARDS & STORAGE: Store in a cool, dry, well ventilated place. INCOMPATIBILITIES: Acids, Bromine trifluoride, Bromine, Bromoform, Carbon, Chloroform, Chromium oxide, Chromium trioxide, Chromyl chloride, Dioxygen difluoride, Fluorine oxide, Hydrogen peroxide, 2-Methyl-1,2-butadiene, NaOBr, Nitric acid, Nitrosyl chloride, Nitrosyl perchlorate, Nitryl perchlorate, NOCl, Oxidizing materials, Permonosulfuric acid, Peroxomonosulfuric acid, Potassium-tert-butoxide, Sulfur dichloride, Sulfuric acid, thio-Diglycol, Thiotrithiazyl perchlorate, Trichloromelamine, 2,4,6-Trichloro-1,3,5-triazine -
TPN Electrolytes (Multiple Electrolyte Additive)
SAFETY DATA SHEET Product Name: TPN Electrolytes (Multiple Electrolyte Additive) 1. CHEMICAL PRODUCT AND COMPANY IDENTIFICATION Manufacturer Name And Hospira, Inc. Address 275 North Field Drive Lake Forest, Illinois 60045 USA Emergency Telephone CHEMTREC: North America: 800-424-9300; International 1-703-527-3887; Australia - 61-290372994; UK - 44-870-8200418 Hospira, Inc., Non-Emergency 224 212-2000 Product Name TPN Electrolytes (Multiple Electrolyte Additive) Synonyms NA 2. HAZARD(S) IDENTIFICATION Emergency Overview TPN Electrolytes (Multiple Electrolyte Additive) is a concentrated solution of intra- and extracellular ions for intravenous infusion after dilution. In clinical use, this product is used to maintain normal cellular metabolism by supplying sodium, calcium, potassium, magnesium, chloride and acetate to the body during total parenteral nutrition (TPN). In the workplace, this material should be considered potentially irritating to the eyes and respiratory tract. Based on clinical use, possible target organs include the nervous system, the cardiovascular system, and muscles. U.S. OSHA GHS Classification Physical Hazards Hazard Class Hazard Category Not Classified Not Classified Health Hazards Hazard Class Hazard Category Eye Damage / Irritation 2B Label Element(s) Pictogram NA Signal Word Warning Hazard Statement(s) Causes eye irritation Precautionary Statement(s) Prevention Do not breathe vapor or spray Wash hands thoroughly after handling Response Get medical attention if you feel unwell. IF IN EYES: Rinse cautiously with -
Tatp) Precursors and Synthetic By-Products
University of Central Florida STARS Electronic Theses and Dissertations, 2004-2019 2009 The Forensic Analysis Of Triacetone Triperoxide (tatp) Precursors And Synthetic By-products Kimberly Painter University of Central Florida Part of the Chemistry Commons, and the Forensic Science and Technology Commons Find similar works at: https://stars.library.ucf.edu/etd University of Central Florida Libraries http://library.ucf.edu This Masters Thesis (Open Access) is brought to you for free and open access by STARS. It has been accepted for inclusion in Electronic Theses and Dissertations, 2004-2019 by an authorized administrator of STARS. For more information, please contact [email protected]. STARS Citation Painter, Kimberly, "The Forensic Analysis Of Triacetone Triperoxide (tatp) Precursors And Synthetic By- products" (2009). Electronic Theses and Dissertations, 2004-2019. 4047. https://stars.library.ucf.edu/etd/4047 THE FORENSIC ANALYSIS OF TRIACETONE TRIPEROXIDE (TATP) PRECURSORS AND SYNTHETIC BY-PRODUCTS by KIMBERLY LYNNE PAINTER B.S. University of South Carolina, 2007 A thesis submitted in partial fulfillment of the requirements for the degree of Master of Science in the Department of Chemistry in the College of Sciences at the University of Central Florida Orlando, Florida Fall Term 2009 © 2009 Kimberly L. Painter ii ABSTRACT Triacetone Triperoxide (TATP) is a primary high explosive that can be synthesized using commercially available starting materials and has grown in use among terrorists over the past several years. Additives present in the precursors were investigated to see if they carry through the TATP synthesis and can be detected in the final product potentially aiding in the identification of the source. -
United States Patent (19) 11 4,029,530 Kenney (45 June 14, 1977
United States Patent (19) 11 4,029,530 Kenney (45 June 14, 1977 3,002,012 9/1961 Backensto ..................... 260/.435. A METHOD OF FORMING LEAD STYPHNATE 54 3,301,882 l/1967 Taylor ........................... 260/435 A AMMUNITION PRIMING MIXTURE 3,320, 104 5/1967 Stadler ................................ 149/24 (75 Inventor: Joseph F. Kenney, Bridgeport, Conn. Primary Examiner-Edward A. Miller 73 Assignee: Remington Arms Company, Inc., Attorney, Agent, or Firm-John H. Lewis, Jr.; Nicholas Bridgeport, Conn. Skovran; William L. Ericson 22 Filed: Feb. 12, 1976 (2) Appl. No.: 657,487 57 ABSTRACT Ammunition rim fire priming mixtures are commonly Related U.S. Application Data prepared by mixing normal lead styphnate, a sensitizer, such as tetracene, an oxygen donor such as lead nitrate, 63 Continuation-in-part of Ser. No. 489,704, July 18, and a frictionator such as ground glass. This invention 1974, abandoned. relates to such a mixture and to center fire priming (52 U.S. C. ................................... 149/28; 149/27; mixtures which consist of lead styphnate, tetracene, 149/24 inorganic fuels and barium nitrate and to a method of (51 Int. Cl.' ......................................... C06B 41/06 forming them and is characterized by the use of lead 58) Field of Search ........................ 149/24, 27, 28; styphnate which is formed in situ by the reaction of a 260/435 A water wet mixture of styphnic acid and a lead com pound such as lead oxide (litharge), lead hydroxide, 56) References Cited basic lead carbonate, or lead carbonate. Important UNITED STATES PATENTS advantages of this invention are reduced cost, im 1,443,328 1/1923 Herz ................................... -
Potentially Explosive Chemicals*
Potentially Explosive Chemicals* Chemical Name CAS # Not 1,1’-Diazoaminonaphthalene Assigned 1,1-Dinitroethane 000600-40-8 1,2,4-Butanetriol trinitrate 006659-60-5 1,2-Diazidoethane 000629-13-0 1,3,5-trimethyl-2,4,6-trinitrobenzene 000602-96-0 1,3-Diazopropane 005239-06-5 Not 1,3-Dinitro-4,5-dinitrosobenzene Assigned Not 1,3-dinitro-5,5-dimethyl hydantoin Assigned Not 1,4-Dinitro-1,1,4,4-tetramethylolbutanetetranitrate Assigned Not 1,7-Octadiene-3,5-Diyne-1,8-Dimethoxy-9-Octadecynoic acid Assigned 1,8 –dihydroxy 2,4,5,7-tetranitroanthraquinone 000517-92-0 Not 1,9-Dinitroxy pentamethylene-2,4,6,8-tetramine Assigned 1-Bromo-3-nitrobenzene 000585-79-5 Not 2,2',4,4',6,6'-Hexanitro-3,3'-dihydroxyazobenzene Assigned 2,2-di-(4,4,-di-tert-butylperoxycyclohexyl)propane 001705-60-8 2,2-Dinitrostilbene 006275-02-1 2,3,4,6- tetranitrophenol 000641-16-7 Not 2,3,4,6-tetranitrophenyl methyl nitramine Assigned Not 2,3,4,6-tetranitrophenyl nitramine Assigned Not 2,3,5,6- tetranitroso nitrobenzene Assigned Not 2,3,5,6- tetranitroso-1,4-dinitrobenzene Assigned 2,4,6-Trinitro-1,3,5-triazo benzene 029306-57-8 Not 2,4,6-trinitro-1,3-diazabenzene Assigned Not 2,4,6-Trinitrophenyl trimethylol methyl nitramine trinitrate Assigned Not 2,4,6-Trinitroso-3-methyl nitraminoanisole Assigned 2,4-Dinitro-1,3,5-trimethyl-benzene 000608-50-4 2,4-Dinitrophenylhydrazine 000119-26-6 2,4-Dinitroresorcinol 000519-44-8 2,5-dimethyl-2,5-diydroperoxy hexane 2-Nitro-2-methylpropanol nitrate 024884-69-3 3,5-Dinitrosalicylic acid 000609-99-4 Not 3-Azido-1,2-propylene glycol dinitrate -
Department of Homeland Security (Dhs) Appendix a Chemicals of Interest (Coi)
DEPARTMENT OF HOMELAND SECURITY (DHS) APPENDIX A CHEMICALS OF INTEREST (COI) Acetaldehyde Bromine trifluoride Acetone Cyanohydrin, stabilized Bromothrifluorethylene Acetyl bromide 1,3-Butadiene Acetyl chloride Butane Acetyl iodide Butene Acetylene 1-Butene Acrolein 2-Butene Acrylonitrile 2-Butene-cis Acrylyl chloride 2-Butene-trans Allyl alcohol Butyltrichlorosilane Allylamine Calcium hydrosulfite Allyltrichlorosilane, stabilized Calcium phosphide Aluminum (powder) Carbon disulfide Aluminum Bromide, anhydrous Carbon oxysulfide Aluminum Chloride, anhydrous Carbonyl fluoride Aluminum phosphide Carbonyl sulfide Ammonia (anhydrous) Chlorine Ammonia (conc 20% or greater) Chlorine dioxide Ammonium nitrate, note #1 Chlorine monoxide Ammonium nitrate, note #2 Chlorine pentafluoride Ammonium perchlorate Chlorine trifluoride Ammonium picrate Chloroacetyl chloride Amyltrichlorosilane 2-Chloroethylchloro-methylsulfide Antimony pentafluoride Chloroform Arsenic trichloride Chloromethyl ether Arsine Chloromethyl methyl ether Barium azide 1-Chloropropylene 1,4-Bis(2-chloroethylthio)-n-butane 2-Chloropropylene Bis(2-chloroethylthio) methane Chlorosarin Bis(2-chloroethylthiomethyl)ether Chlorosoman 1,5-Bis(2-chloroethylthio)-n-pentane Chlorosulfonic acid 1,3-Bis(2-chloroethylthio)-n-propane Chromium oxychloride Boron tribromide Crotonaldehyde Boron trichloride Crotonaldehyde, (E)- Boron trifluoride Cyanogen Boron trifluoride compound with methyl Cyanogen chloride ether (1:1) Cyclohexylamine Bromine Cyclohexyltrichlorosilane Bromine chloride Cyclopropane -
Chemical Names and CAS Numbers Final
Chemical Abstract Chemical Formula Chemical Name Service (CAS) Number C3H8O 1‐propanol C4H7BrO2 2‐bromobutyric acid 80‐58‐0 GeH3COOH 2‐germaacetic acid C4H10 2‐methylpropane 75‐28‐5 C3H8O 2‐propanol 67‐63‐0 C6H10O3 4‐acetylbutyric acid 448671 C4H7BrO2 4‐bromobutyric acid 2623‐87‐2 CH3CHO acetaldehyde CH3CONH2 acetamide C8H9NO2 acetaminophen 103‐90‐2 − C2H3O2 acetate ion − CH3COO acetate ion C2H4O2 acetic acid 64‐19‐7 CH3COOH acetic acid (CH3)2CO acetone CH3COCl acetyl chloride C2H2 acetylene 74‐86‐2 HCCH acetylene C9H8O4 acetylsalicylic acid 50‐78‐2 H2C(CH)CN acrylonitrile C3H7NO2 Ala C3H7NO2 alanine 56‐41‐7 NaAlSi3O3 albite AlSb aluminium antimonide 25152‐52‐7 AlAs aluminium arsenide 22831‐42‐1 AlBO2 aluminium borate 61279‐70‐7 AlBO aluminium boron oxide 12041‐48‐4 AlBr3 aluminium bromide 7727‐15‐3 AlBr3•6H2O aluminium bromide hexahydrate 2149397 AlCl4Cs aluminium caesium tetrachloride 17992‐03‐9 AlCl3 aluminium chloride (anhydrous) 7446‐70‐0 AlCl3•6H2O aluminium chloride hexahydrate 7784‐13‐6 AlClO aluminium chloride oxide 13596‐11‐7 AlB2 aluminium diboride 12041‐50‐8 AlF2 aluminium difluoride 13569‐23‐8 AlF2O aluminium difluoride oxide 38344‐66‐0 AlB12 aluminium dodecaboride 12041‐54‐2 Al2F6 aluminium fluoride 17949‐86‐9 AlF3 aluminium fluoride 7784‐18‐1 Al(CHO2)3 aluminium formate 7360‐53‐4 1 of 75 Chemical Abstract Chemical Formula Chemical Name Service (CAS) Number Al(OH)3 aluminium hydroxide 21645‐51‐2 Al2I6 aluminium iodide 18898‐35‐6 AlI3 aluminium iodide 7784‐23‐8 AlBr aluminium monobromide 22359‐97‐3 AlCl aluminium monochloride -
Commerce in Explosives; 2020 Annual Those on the Annual List
Federal Register / Vol. 85, No. 247 / Wednesday, December 23, 2020 / Notices 83999 inspection at the Office of the Secretary or synonyms in brackets. This list Black powder substitutes. and on EDIS.3 supersedes the List of Explosive *Blasting agents, nitro-carbo-nitrates, This action is taken under the Materials published in the Federal including non-cap sensitive slurry and authority of section 337 of the Tariff Act Register on January 2, 2020 (Docket No. water gel explosives. of 1930, as amended (19 U.S.C. 1337), 2019R–04, 85 FR 128). Blasting caps. and of §§ 201.10 and 210.8(c) of the The 2020 List of Explosive Materials Blasting gelatin. Commission’s Rules of Practice and is a comprehensive list, but is not all- Blasting powder. Procedure (19 CFR 201.10, 210.8(c)). inclusive. The definition of ‘‘explosive BTNEC [bis (trinitroethyl) carbonate]. materials’’ includes ‘‘[e]xplosives, BTNEN [bis (trinitroethyl) nitramine]. By order of the Commission. BTTN [1,2,4 butanetriol trinitrate]. Issued: December 18, 2020. blasting agents, water gels and detonators. Explosive materials, Bulk salutes. William Bishop, include, but are not limited to, all items Butyl tetryl. Supervisory Hearings and Information in the ‘List of Explosive Materials’ Officer. C provided for in § 555.23.’’ 27 CFR Calcium nitrate explosive mixture. [FR Doc. 2020–28458 Filed 12–22–20; 8:45 am] 555.11. Accordingly, the fact that an BILLING CODE 7020–02–P Cellulose hexanitrate explosive explosive material is not on the annual mixture. list does not mean that it is not within Chlorate explosive mixtures. coverage of the law if it otherwise meets DEPARTMENT OF JUSTICE Composition A and variations.