List of Dual-Use Goods and Technologies and Munitions List
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Federal Register/Vol. 80, No. 116
34572 Federal Register / Vol. 80, No. 116 / Wednesday, June 17, 2015 / Proposed Rules Related Definitions: N/A SUMMARY: As part of the President’s Arms Regulations (ITAR) (22 CFR parts Items: Export Control Reform effort, the 120–130). The items subject to the The list of items controlled is contained in Department of State proposes to amend jurisdiction of the ITAR, i.e., ‘‘defense the ECCN heading. the International Traffic in Arms articles,’’ are identified on the ITAR’s ■ 9. In Supplement No. 1 to Part 774 Regulations (ITAR) to revise Categories U.S. Munitions List (USML) (22 CFR (the Commerce Control List), Category XIV (toxicological agents, including 121.1). With few exceptions, items not 6—Sensors and Lasers,’’ add a new chemical agents, biological agents, and subject to the export control jurisdiction ECCN 6E619 between ECCNs 6E202 and associated equipment) and XVIII of the ITAR are subject to the 6E990 to read as follows: (directed energy weapons) of the U.S. jurisdiction of the Export 6E619 ‘‘Technology’’ ‘‘required’’ for the Munitions List (USML) to describe more Administration Regulations (‘‘EAR,’’ 15 ‘‘development,’’ ‘‘production,’’ precisely the articles warranting control CFR parts 730–774, which includes the operation, installation, maintenance, on the USML. The revisions contained Commerce Control List (CCL) in repair, overhaul or refurbishing of in this rule are part of the Department Supplement No. 1 to Part 774), commodities controlled by 6B619 or of State’s retrospective plan under E.O. administered by the Bureau of Industry ‘‘software’’ controlled by 6D619. 13563 completed on August 17, 2011. and Security (BIS), U.S. -
Aldrich Vapor
Aldrich Vapor Library Listing – 6,611 spectra This library is an ideal tool for investigator using FT-IR to analyze gas phase materials. It contains gas phase spectra collected by Aldrich using a GC-IR interface to ensure chromatographically pure samples. The Aldrich FT-IR Vapor Phase Library contains 6,611 gas phase FT-IR spectra collected by Aldrich Chemical Company using a GC interface. The library includes compound name, molecular formula, CAS (Chemical Abstract Service) registry number, Aldrich catalog number, and page number in the Aldrich Library of FT-IR Spectra, Edition 1, Volume 3, Vapor-Phase. Aldrich Vapor Index Compound Name Index Compound Name 6417 ((1- 3495 (1,2-Dibromoethyl)benzene; Styrene Ethoxycyclopropyl)oxy)trimethylsilane dibromide 2081 (+)-3-(Heptafluorobutyryl)camphor 3494 (1-Bromoethyl)benzene; 1-Phenylethyl 2080 (+)-3-(Trifluoroacetyl)camphor bromide 262 (+)-Camphene; 2,2-Dimethyl-3- 6410 (1-Hydroxyallyl)trimethylsilane methylenebicyclo[2.2.1]heptane 6605 (1-Methyl-2,4-cyclopentadien-1- 2828 (+)-Diisopropyl L-tartrate yl)manganese tricarbonyl 947 (+)-Isomenthol; [1S-(1a,2b,5b)]-2- 6250 (1-Propynyl)benzene; 1-Phenylpropyne Isopropyl-5-methylcyclohexano 2079 (1R)-(+)-3-Bromocamphor, endo- 1230 (+)-Limonene oxide, cis + trans; (+)-1,2- 2077 (1R)-(+)-Camphor; (1R)-(+)-1,7,7- Epoxy-4-isopropenyl-1- Trimethylbicyclo[2.2.1]heptan- 317 (+)-Longifolene; (1S)-8-Methylene- 976 (1R)-(+)-Fenchyl alcohol, endo- 3,3,7-trimethyltricyclo[5.4.0 2074 (1R)-(+)-Nopinone; (1R)-(+)-6,6- 949 (+)-Menthol; [1S-(1a,2b,5a)]-(+)-2- Dimethylbicyclo[3.1.1]heptan-2- -
Critical Evaluation of Proven Chemical Weapon Destruction Technologies
Pure Appl. Chem., Vol. 74, No. 2, pp. 187–316, 2002. © 2002 IUPAC INTERNATIONAL UNION OF PURE AND APPLIED CHEMISTRY ORGANIC AND BIOMOLECULAR CHEMISTRY DIVISION IUPAC COMMITTEE ON CHEMICAL WEAPON DESTRUCTION TECHNOLOGIES* WORKING PARTY ON EVALUATION OF CHEMICAL WEAPON DESTRUCTION TECHNOLOGIES** CRITICAL EVALUATION OF PROVEN CHEMICAL WEAPON DESTRUCTION TECHNOLOGIES (IUPAC Technical Report) Prepared for publication by GRAHAM S. PEARSON1,‡ AND RICHARD S. MAGEE2 1Department of Peace Studies, University of Bradford, Bradford, West Yorkshire BD7 1DP, UK 2Carmagen Engineering, Inc., 4 West Main Street, Rockaway, NJ 07866, USA *Membership of the IUPAC Committee is: Chairman: Joseph F. Burnett; Members: Wataru Ando (Japan), Irina P. Beletskaya (Russia), Hongmei Deng (China), H. Dupont Durst (USA), Daniel Froment (France), Ralph Leslie (Australia), Ronald G. Manley (UK), Blaine C. McKusick (USA), Marian M. Mikolajczyk (Poland), Giorgio Modena (Italy), Walter Mulbry (USA), Graham S. Pearson (UK), Kurt Schaffner (Germany). **Membership of the Working Group was as follows: Chairman: Graham S. Pearson (UK); Members: Richard S. Magee (USA), Herbert de Bisschop (Belgium). The Working Group wishes to acknowledge the contributions made by the following, although the conclusions and contents of the Technical Report remain the responsibility of the Working Group: Joseph F. Bunnett (USA), Charles Baronian (USA), Ron G. Manley (OPCW), Georgio Modena (Italy), G. P. Moss (UK), George W. Parshall (USA), Julian Perry Robinson (UK), and Volker Starrock (Germany). ‡Corresponding author Republication or reproduction of this report or its storage and/or dissemination by electronic means is permitted without the need for formal IUPAC permission on condition that an acknowledgment, with full reference to the source, along with use of the copyright symbol ©, the name IUPAC, and the year of publication, are prominently visible. -
Aldrich Raman
Aldrich Raman Library Listing – 14,033 spectra This library represents the most comprehensive collection of FT-Raman spectral references available. It contains many common chemicals found in the Aldrich Handbook of Fine Chemicals. To create the Aldrich Raman Condensed Phase Library, 14,033 compounds found in the Aldrich Collection of FT-IR Spectra Edition II Library were excited with an Nd:YVO4 laser (1064 nm) using laser powers between 400 - 600 mW, measured at the sample. A Thermo FT-Raman spectrometer (with a Ge detector) was used to collect the Raman spectra. The spectra were saved in Raman Shift format. Aldrich Raman Index Compound Name Index Compound Name 4803 ((1R)-(ENDO,ANTI))-(+)-3- 4246 (+)-3-ISOPROPYL-7A- BROMOCAMPHOR-8- SULFONIC METHYLTETRAHYDRO- ACID, AMMONIUM SALT PYRROLO(2,1-B)OXAZOL-5(6H)- 2207 ((1R)-ENDO)-(+)-3- ONE, BROMOCAMPHOR, 98% 12568 (+)-4-CHOLESTEN-3-ONE, 98% 4804 ((1S)-(ENDO,ANTI))-(-)-3- 3774 (+)-5,6-O-CYCLOHEXYLIDENE-L- BROMOCAMPHOR-8- SULFONIC ASCORBIC ACID, 98% ACID, AMMONIUM SALT 11632 (+)-5-BROMO-2'-DEOXYURIDINE, 2208 ((1S)-ENDO)-(-)-3- 97% BROMOCAMPHOR, 98% 11634 (+)-5-FLUORODEOXYURIDINE, 769 ((1S)-ENDO)-(-)-BORNEOL, 99% 98+% 13454 ((2S,3S)-(+)- 11633 (+)-5-IODO-2'-DEOXYURIDINE, 98% BIS(DIPHENYLPHOSPHINO)- 4228 (+)-6-AMINOPENICILLANIC ACID, BUTANE)(N3-ALLYL)PD(II) CL04, 96% 97 8167 (+)-6-METHOXY-ALPHA-METHYL- 10297 ((3- 2- NAPHTHALENEACETIC ACID, DIMETHYLAMINO)PROPYL)TRIPH 98% ENYL- PHOSPHONIUM BROMIDE, 12586 (+)-ANDROSTA-1,4-DIENE-3,17- 99% DIONE, 98% 13458 ((R)-(+)-2,2'- 963 (+)-ARABINOGALACTAN BIS(DIPHENYLPHOSPHINO)-1,1'- -
War Gases .Pdf
yh&% .*i From the collection of the m Prejinger h v Jjibrary San Francisco, California 2007 THE WAR GASES WAR GASES Their Identification and Decontamination BY MORRIS B. JACOBS, Ph.D. Food, Drug and Insecticide Admin. U. S. Dept. of Agr. 1927 Chemist Department of Health, City of New York, 1928. Formerly, Lt. U. S. Chemical Warfare Service Reserve INTERSCIENCE PUBLISHERS, INC. NEW YORK, N. Y.-1942 Copyright, 1942, by INTERSCIENCE PUBLISHERS, INC. 215 Fourth Avenue, New York, N. Y. Printed in U. S. A. by WAVERLY PRESS, BALTIMORE, MD. PREFACE Relatively little has been written in the United States of America on the subject of passive defense, or as we would put it, civilian defense against poison gas. One of the very first steps in defense of this nature is a system for the detection, the sampling and the identification of the chemical war- fare agents, and the decontamination of areas and materials polluted by them. It is the aim of this book to present these subjects so that the informa- tion given will be useful to the gas identification officer, the war gas chemist, the decontamination officer, and the health officer. While this book was written primarily for the aforementioned officers, Chapters I, II, III, part of IV and VII should prove of value to the air raid warden and, in general, to all persons dealing with the above mentioned phases of gas defense. It is written so that it can be used for the training of gas identifi- cation officers, as a manual by chemists and decontamination officers, and as a source of information on the analytical chemistry of the war gases. -
Christian Gloor Journal Club Group Meeting 16 01 2014 .01.2014
Christian Gloor Journal Club Group Meeting 16.01 . 2014 Definitions • Chemical Weapons (CW): − Toxic chemicals and their precursors, except where intended for purposes not prohibited under the convention, as long as the types and quantities are consistent with such purposes − Munitions and devices, specially designed to cause death or other harm • Purposes not prohibited under the convention − Industrial, agricultural, research, medicinal, pharmaceutical or other peaceful purposes − Protective purposes, namely against chemical weapons OPCW Convention on the prohibition of the development, production, stockpiling and use of chemical weapons and on their destruction, Version 2013 Classes of chemical warfare agents y Harassing agents O Cl Cl CN CN Chloracetophenone (CN) Ortho-chlorobenzylidene malononitrile (CS) OH H N Br O O Benzyl bromide Capsaicin (OC) H Cl N As As Cl Diphenylchloroarsine (DA) Adamsite (DM) Classes of chemical warfare agents y Incapacitating agents y Choking agents y Blood agents hdhydrogen cyanide (AC); AAirsine (SA); cyanogen chlor ide (CK) Classes of chemical warfare agents y Blister agents Cl Cl N S As Cl Cl Cl Cl Cl Cl Tris(2-chloroethyl)amine (HN3) Bis(2-chloroethyl) sulfide (HD) 2-Chlorovinyldichloroarsine (L) S S S Cl Cl O Cl Cl S Bis(2-chloroethylthioethyl) ether (T) 1,2-Bis(2-chloroethylthio) ethane (Q) Symptoms of blister agents Classes of chemical warfare agents y Nerve agents Mode of action of nerve agents Antidotes for nerve agents N O O OH Atropin Cl H N O N H Cl N N O O Obidoxim chloride Antidotes y For blister agents A mixture of bleaching powder with 35% active chlorine, molecular sieve, magnesium oxide and silica. -
Scientific Advisory Board
OPCW Scientific Advisory Board Eleventh Session SAB-11/1 11 – 13 February 2008 13 February 2008 Original: ENGLISH REPORT OF THE ELEVENTH SESSION OF THE SCIENTIFIC ADVISORY BOARD 1. AGENDA ITEM ONE – Opening of the Session The Scientific Advisory Board (SAB) met for its Eleventh Session from 11 to 13 February 2008 at the OPCW headquarters in The Hague, the Netherlands. The Session was opened by the Vice-Chairperson of the SAB, Mahdi Balali-Mood. The meeting was chaired by Philip Coleman of South Africa, and Mahdi Balali-Mood of the Islamic Republic of Iran served as Vice-Chairperson. A list of participants appears as Annex 1 to this report. 2. AGENDA ITEM TWO – Adoption of the agenda 2.1 The SAB adopted the following agenda for its Eleventh Session: 1. Opening of the Session 2. Adoption of the agenda 3. Tour de table to introduce new SAB Members 4. Election of the Chairperson and the Vice-Chairperson of the SAB1 5. Welcome address by the Director-General 6. Overview on developments at the OPCW since the last session of the SAB 7. Establishment of a drafting committee 8. Work of the temporary working groups: (a) Consideration of the report of the second meeting of the sampling-and-analysis temporary working group; 1 In accordance with paragraph 1.1 of the rules of procedure for the SAB and the temporary working groups of scientific experts (EC-XIII/DG.2, dated 20 October 1998) CS-2008-5438(E) distributed 28/02/2008 *CS-2008-5438.E* SAB-11/1 page 2 (b) Status report by the Industry Verification Branch on the implementation of sampling and analysis for Article VI inspections; (c) Presentation by the OPCW Laboratory; (d) Update on education and outreach; and (e) Update on the formation of the temporary working group on advances in science and technology and their potential impact on the implementation of the Convention: (i) composition of the group; and (ii) its terms of reference 9. -
United States Patent (19) 11 4,362,884 Arkles (45) Dec
United States Patent (19) 11 4,362,884 Arkles (45) Dec. 7, 1982 (54) SILACROWN ETHERS, METHOD OF MAKING SAME, AND USE AS OTHER PUBLICATIONS PHASE-TRANSFER CATALYSTS C. J. Pederson, J. Am. Chem. Soc., 89, 7017, (1967). R. Kieble, C. Burkhard, J. Am. Chem. Soc., 69, 2689, (75) Inventor: Barry C. Arkles, Oreland, Pa. (1947). (73) Assignee: Petrarch Systems, Inc., Levittown, Primary Examiner-Paul F. Shaver Pa. Attorney, Agent, or Firm-Seidel, Gonda, Goldhammer & Panitch 21) Appl. No.: 323,629 57 ABSTRACT 22 Filed: Nov. 23, 1981 Organosilicon compounds referred to as silacrown ethers or "silacrowns' are of the general formula: (51) Int. Cl............................. C07F 7/08; C07F 7/18 52) U.S. C. .................................... 556/446; 260/464; 560/236; 570/143; 570/145; 570/191; 570/196; 570/197; 570/261 58 Field of Search ......................................... 556/446 where R1 and R2 are organic radicals or hydrogen and 56 References Cited n is an integer between 4 and 10 inclusive. Silacrown U.S. PATENT DOCUMENTS ethers are prepared by reacting polyethylene glycol 3,078,293 2/1963 Ender .................................. 556/446 with substituted silanes under conditions promoting 3,475,478 10/1969 Simmler ..... 556/446X cyclization over polymerization. Silacrown ethers may 3,505,380 4/1970 Berger ................................. 556/446 be employed as phase-transfer catalysts in solution or 3,539,610 1 1/1970 Berger ............................ 536/446X immobilized on siliceous supports. 3,987,061 10/1976 Pedersen ......................... 556/446X 4,098,808 7/1978 Wolfers et al. ..................... 556/446 12 Claims, No Drawings 4,362,884 1 2 SILACROWNETHERS, METHOD OF MAKING DETAILED DESCRIPTION OF THE SAME, AND USE AS PHASE-TRANSFER INVENTION CATALYSTS Silacrowns exhibit complexation properties remark 5 ably similar to crown ethers. -
Preparation of 2-Phenylcyclohexanone and Substituted 2-Arylcyclohenanones
THE PREPARATION OP 2-PHENYLCYCL0HEXAN0NE AND SUBSTITUTED 2-ARYLCYCL0HENAN0NES i . by J RICHARD GRANT HIS KEY A. B., Kansas State Teachers College, Emporia, 1951 A THESIS submitted in partial fulfillment of the requirements for the degree MASTER OP SCIENCE Department of Chemistry KANSAS STATE COLLEGE OF AGRICULTURE AND APPLIED SCIENCE 1953 ii QJUtt A- ViW3» c.cl table op contents I introduction 1 purpose of the investigation 16 results of the investigation ,16 Isolation and Identification of the Intermediate Chlorohydrins 16 Comparison of the Rearrangement of the Cis- and Trans - Chlorohydrins 28 Preparation of Some New 2-Arylcyclohexanones 31 EXPERIMENTAL , . 43 Isolation and Identification of the Intermediate Chlorohydrins 43 Rearrangement of the Cis and Trans Chlorohydrins to 2-Phenylcyclohenanone 49 Preparation of Some New 2-Arylcyclohexanones 51 ACKNOWLEDGMENT 63 BIBLIOGRAPHY 64 INTRODUCTION In recent years both partial syntheses and total syntheses of natural products have become increasingly important. The total synthesis of these products is very desirable since total synthesis of a compound affords a method by which final, con- clusive proof of its structure may be obtained. In addition, the total synthesis might prove economically feasible. For these reasons many workers have attempted to totally synthesize various natural products and their analogs. One of the outstanding examples of the synthesis of a rel- atively complex natural product was that of the female sex hor- mone, equilinln (II), by Bachmann, Cole, and Wilds (1) in 1959- 1940. The last portion of this synthesis utilized the cyclic ketone, 7-methoxy-l-keto-l ,2,5,4 tetrahydro phenanthrene (I) as a key Intermediate. -
WO 2016/147132 Al 22 September 2016 (22.09.2016) P O P C T
(12) INTERNATIONAL APPLICATION PUBLISHED UNDER THE PATENT COOPERATION TREATY (PCT) (19) World Intellectual Property Organization International Bureau (10) International Publication Number (43) International Publication Date WO 2016/147132 Al 22 September 2016 (22.09.2016) P O P C T (51) International Patent Classification: (81) Designated States (unless otherwise indicated, for every C07C 227/32 (2006.01) C07D 405/04 (2006.01) kind of national protection available): AE, AG, AL, AM, AO, AT, AU, AZ, BA, BB, BG, BH, BN, BR, BW, BY, (21) International Application Number: BZ, CA, CH, CL, CN, CO, CR, CU, CZ, DE, DK, DM, PCT/IB20 16/05 14 1 DO, DZ, EC, EE, EG, ES, FI, GB, GD, GE, GH, GM, GT, (22) International Filing Date: HN, HR, HU, ID, IL, IN, IR, IS, JP, KE, KG, KN, KP, KR, 17 March 2016 (17.03.2016) KZ, LA, LC, LK, LR, LS, LU, LY, MA, MD, ME, MG, MK, MN, MW, MX, MY, MZ, NA, NG, NI, NO, NZ, OM, (25) Filing Language: English PA, PE, PG, PH, PL, PT, QA, RO, RS, RU, RW, SA, SC, (26) Publication Language: English SD, SE, SG, SK, SL, SM, ST, SV, SY, TH, TJ, TM, TN, TR, TT, TZ, UA, UG, US, UZ, VC, VN, ZA, ZM, ZW. (30) Priority Data: 895/MUM/2015 18 March 2015 (18.03.2015) (84) Designated States (unless otherwise indicated, for every kind of regional protection available): ARIPO (BW, GH, (71) Applicant: PIRAMAL ENTERPRISES LIMITED GM, KE, LR, LS, MW, MZ, NA, RW, SD, SL, ST, SZ, [IN/IN]; Piramal Tower, Ganpatrao Kadam Marg, Lower TZ, UG, ZM, ZW), Eurasian (AM, AZ, BY, KG, KZ, RU, Parel, Mumbai 400 013 (IN). -
The Use of Natural Product Substrates for the Synthesis of Libraries of Biologically Active, New Chemical Entities
University of Montana ScholarWorks at University of Montana Graduate Student Theses, Dissertations, & Graduate School Professional Papers 2010 The seU of Natural Product Substrates for the Synthesis of Libraries of Biologically Active, New Chemical Entities Joshua Bryant Phillips The University of Montana Let us know how access to this document benefits ouy . Follow this and additional works at: https://scholarworks.umt.edu/etd Recommended Citation Phillips, Joshua Bryant, "The sU e of Natural Product Substrates for the Synthesis of Libraries of Biologically Active, New Chemical Entities" (2010). Graduate Student Theses, Dissertations, & Professional Papers. 1100. https://scholarworks.umt.edu/etd/1100 This Dissertation is brought to you for free and open access by the Graduate School at ScholarWorks at University of Montana. It has been accepted for inclusion in Graduate Student Theses, Dissertations, & Professional Papers by an authorized administrator of ScholarWorks at University of Montana. For more information, please contact [email protected]. THE USE OF NATURAL PRODUCT SUBSTRATES FOR THE SYNTHESIS OF LIBRARIES OF BIOLOGICALLY ACTIVE, NEW CHEMICAL ENTITIES by Joshua Bryant Phillips B.S. Chemistry, Northern Arizona University, 2002 B.S. Microbiology (health pre-professional), Northern Arizona University, 2002 Presented in partial fulfillment of the requirements for the degree of Doctor of Philosophy Chemistry The University of Montana June 2010 Phillips, Joshua Bryant Ph.D., June 2010 Chemistry THE USE OF NATURAL PRODUCT SUBSTRATES FOR THE SYNTHESIS OF LIBRARIES OF BIOLOGICALLY ACTIVE, NEW CHEMICAL ENTITIES Advisor: Dr. Nigel D. Priestley Chairperson: Dr. Bruce Bowler ABSTRACT Since Alexander Fleming first noted the killing of a bacterial culture by a mold, antibiotics have revolutionized medicine, being able to treat, and often cure life-threatening illnesses and making surgical procedures possible by eliminating the possibility of opportunistic infection. -
ITAR Category
Category XIV—Toxicological Agents, Including Chemical Agents, Biological Agents, and Associated Equipment *(a) Chemical agents, to include: (1) Nerve agents: (i) O-Alkyl (equal to or less than C10, including cycloalkyl) alkyl (Methyl, Ethyl, n-Propyl or Isopropyl)phosphonofluoridates, such as: Sarin (GB): O-Isopropyl methylphosphonofluoridate (CAS 107–44–8) (CWC Schedule 1A); and Soman (GD): O-Pinacolyl methylphosphonofluoridate (CAS 96–64–0) (CWC Schedule 1A); (ii) O-Alkyl (equal to or less than C10, including cycloalkyl) N,N-dialkyl (Methyl, Ethyl, n- Propyl or Isopropyl)phosphoramidocyanidates, such as: Tabun (GA): O-Ethyl N, N- dimethylphosphoramidocyanidate (CAS 77–81–6) (CWC Schedule 1A); (iii) O-Alkyl (H or equal to or less than C10, including cycloalkyl) S–2-dialkyl (Methyl, Ethyl, n- Propyl or Isopropyl)aminoethyl alkyl (Methyl, Ethyl, n-Propyl or Isopropyl)phosphonothiolates and corresponding alkylated and protonated salts, such as: VX: O-Ethyl S-2- diisopropylaminoethyl methyl phosphonothiolate (CAS 50782–69–9) (CWC Schedule 1A); (2) Amiton: O,O-Diethyl S-[2(diethylamino)ethyl] phosphorothiolate and corresponding alkylated or protonated salts (CAS 78–53–5) (CWC Schedule 2A); (3) Vesicant agents: (i) Sulfur mustards, such as: 2-Chloroethylchloromethylsulfide (CAS 2625–76–5) (CWC Schedule 1A); Bis(2-chloroethyl)sulfide (CAS 505–60–2) (CWC Schedule 1A); Bis(2- chloroethylthio)methane (CAS 63839–13–6) (CWC Schedule 1A); 1,2-bis (2- chloroethylthio)ethane (CAS 3563–36–8) (CWC Schedule 1A); 1,3-bis (2-chloroethylthio)-n- propane (CAS