Federal Register/Vol. 76, No. 202/Wednesday, October 19, 2011
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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. -
Trinitrobenzene
doi: 10.5028/jatm.2011.03010411 Gilson da Silva* National Industrial Property Institute Synthesis of 2,4,6-triamino-1,3,5- Rio de Janeiro – Brazil [email protected] trinitrobenzene Elizabeth da Costa Mattos Abstract: The 2,4,6-triamino-1,3,5-trinitrobenzene (TATB) is perhaps the Institute of Aeronautics and Space most thermostable and insensitive explosive known. Its low sensibility to São José dos Campos – Brazil shock makes it suitable for military and civil applications. TATB application [email protected] is done either alone or in combination with another high energetic material. This study aimed at reporting the review about many processes to produce *author for correspondence TATB and the problems associated with them, as well as suggest techniques like Fourier Transform Infrared Spectroscopy (FT-IR) and Differential Scanning Calorimetry (DSC), which can be useful in the characterization of this energetic compound. Keywords: TATB, Fourier Transform Infrared Spectroscopy, Differential Scanning Calorimetry, Plastic-bonded explosive. LIST OF SYMBOLS impact hazards is important. Other potential applications include the use of TATB as the booster or main charge TATB 2,4,6-triamino-1,3,5-trinitrobenzene explosives for down-hole oil perforation at elevated HE high explosive temperature surroundings (Lee, 1996). PBX plastic-bonded explosive HMX octogen TATB is a high explosive (HE) that can be combined with plastic binder to produce a plastic-bonded explosive RDX hexogen (PBX) composition, which is heat-resistant and highly TCB 1,3,5-trichlorobenzene insensitive. It is insoluble in organic solvents and has a TCTNB 1,3,5-trichloro-2,4,6-trinitrobenzene melting point above 400oC. -
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 -
Pharmaceutical Appendix to the Tariff Schedule 2
Harmonized Tariff Schedule of the United States (2007) (Rev. 2) Annotated for Statistical Reporting Purposes PHARMACEUTICAL APPENDIX TO THE HARMONIZED TARIFF SCHEDULE Harmonized Tariff Schedule of the United States (2007) (Rev. 2) Annotated for Statistical Reporting Purposes PHARMACEUTICAL APPENDIX TO THE TARIFF SCHEDULE 2 Table 1. This table enumerates products described by International Non-proprietary Names (INN) which shall be entered free of duty under general note 13 to the tariff schedule. The Chemical Abstracts Service (CAS) registry numbers also set forth in this table are included to assist in the identification of the products concerned. For purposes of the tariff schedule, any references to a product enumerated in this table includes such product by whatever name known. ABACAVIR 136470-78-5 ACIDUM LIDADRONICUM 63132-38-7 ABAFUNGIN 129639-79-8 ACIDUM SALCAPROZICUM 183990-46-7 ABAMECTIN 65195-55-3 ACIDUM SALCLOBUZICUM 387825-03-8 ABANOQUIL 90402-40-7 ACIFRAN 72420-38-3 ABAPERIDONUM 183849-43-6 ACIPIMOX 51037-30-0 ABARELIX 183552-38-7 ACITAZANOLAST 114607-46-4 ABATACEPTUM 332348-12-6 ACITEMATE 101197-99-3 ABCIXIMAB 143653-53-6 ACITRETIN 55079-83-9 ABECARNIL 111841-85-1 ACIVICIN 42228-92-2 ABETIMUSUM 167362-48-3 ACLANTATE 39633-62-0 ABIRATERONE 154229-19-3 ACLARUBICIN 57576-44-0 ABITESARTAN 137882-98-5 ACLATONIUM NAPADISILATE 55077-30-0 ABLUKAST 96566-25-5 ACODAZOLE 79152-85-5 ABRINEURINUM 178535-93-8 ACOLBIFENUM 182167-02-8 ABUNIDAZOLE 91017-58-2 ACONIAZIDE 13410-86-1 ACADESINE 2627-69-2 ACOTIAMIDUM 185106-16-5 ACAMPROSATE 77337-76-9 -
Redalyc.Synthesis of 2,4,6-Triamino-1,3,5-Trinitrobenzene
Journal of Aerospace Technology and Management ISSN: 1948-9648 [email protected] Instituto de Aeronáutica e Espaço Brasil da Silva, Gilson; da Costa Mattos, Elizabeth Synthesis of 2,4,6-triamino-1,3,5-trinitrobenzene Journal of Aerospace Technology and Management, vol. 3, núm. 1, enero-abril, 2011, pp. 65-72 Instituto de Aeronáutica e Espaço São Paulo, Brasil Available in: http://www.redalyc.org/articulo.oa?id=309426555007 How to cite Complete issue Scientific Information System More information about this article Network of Scientific Journals from Latin America, the Caribbean, Spain and Portugal Journal's homepage in redalyc.org Non-profit academic project, developed under the open access initiative doi: 10.5028/jatm.2011.03010411 Gilson da Silva* National Industrial Property Institute Synthesis of 2,4,6-triamino-1,3,5- Rio de Janeiro – Brazil [email protected] trinitrobenzene Elizabeth da Costa Mattos Abstract: The 2,4,6-triamino-1,3,5-trinitrobenzene (TATB) is perhaps the Institute of Aeronautics and Space most thermostable and insensitive explosive known. Its low sensibility to São José dos Campos – Brazil shock makes it suitable for military and civil applications. TATB application [email protected] is done either alone or in combination with another high energetic material. This study aimed at reporting the review about many processes to produce *author for correspondence TATB and the problems associated with them, as well as suggest techniques like Fourier Transform Infrared Spectroscopy (FT-IR) and Differential Scanning Calorimetry (DSC), which can be useful in the characterization of this energetic compound. Keywords: TATB, Fourier Transform Infrared Spectroscopy, Differential Scanning Calorimetry, Plastic-bonded explosive. -
Prediction of the Crystalline Densities of Aliphatic Nitrates by Quantum Chemistry Methods
Central European Journal of Energetic Materials ISSN 1733-7178; e-ISSN 2353-1843 Copyright © 2019 Sieć Badawcza Łukasiewicz – Institute of Industrial Organic Chemistry, Poland Cent. Eur. J. Energ. Mater. 2019, 16(3): 412-432; DOI 10.22211/cejem/112306 Article is available in PDF-format, in colour, at: http://www.wydawnictwa.ipo.waw.pl/cejem/Vol-16-Number3-2019/CEJEM_00978.pdf Article is available under the Creative Commons Attribution-Noncommercial-NoDerivs 3.0 license CC BY-NC-ND 3.0. Research paper Prediction of the Crystalline Densities of Aliphatic Nitrates by Quantum Chemistry Methods Guixiang Wang,* Yimin Xu, Chuang Xue, Zhiyuan Ding, Yan Liu, Hui Liu, Xuedong Gong** Computation Institute for Molecules and Materials, Department of Chemistry, Nanjing University of Science and Technology, Nanjing 210094, China E-mails: * [email protected]; ** [email protected] Abstract: Crystal density is a basic and important parameter for predicting the detonation performance of explosives, and nitrate esters are a type of compound widely used in the military context. In this study, thirty-one aliphatic nitrates were investigated using the density functional theory method (B3LYP) in combination with six basis sets (3-21G, 6-31G, 6-31G*, 6-31G**, 6-311G* and 6-31+G**) and the semiempirical molecular orbital method (PM3). Based on the geometric optimizations at various theoretical levels, the molecular volumes and densities were calculated. Compared with the available experimental data, the densities calculated by various methods are all overestimated, and the errors of the PM3 and B3LYP/3-21G methods are larger than those of other methods. Considering the results and the computer resources required by the calculations, the B3LYP/6-31G* method is recommended for predicting the crystalline densities of organic nitrates using a fitting equation. -
Compositions Comprising Nebivolol
(19) TZZ ZZ__T (11) EP 2 808 015 A1 (12) EUROPEAN PATENT APPLICATION (43) Date of publication: (51) Int Cl.: 03.12.2014 Bulletin 2014/49 A61K 31/34 (2006.01) A61K 31/502 (2006.01) A61K 31/353 (2006.01) A61P 9/00 (2006.01) (21) Application number: 14002458.9 (22) Date of filing: 16.11.2005 (84) Designated Contracting States: • O’Donnell, John AT BE BG CH CY CZ DE DK EE ES FI FR GB GR Morgantown, WV 26505 (US) HU IE IS IT LI LT LU LV MC NL PL PT RO SE SI • Bottini, Peter Bruce SK TR Morgantown, WV 26505 (US) • Mason, Preston (30) Priority: 31.05.2005 US 141235 Morgantown, WV 26504 (US) 10.11.2005 US 272562 • Shaw, Andrew Preston 15.11.2005 US 273992 Morgantown, WV 26504 (US) (62) Document number(s) of the earlier application(s) in (74) Representative: Samson & Partner accordance with Art. 76 EPC: Widenmayerstraße 5 09015249.7 / 2 174 658 80538 München (DE) 05848185.4 / 1 890 691 Remarks: (71) Applicant: MYLAN LABORATORIES, INC This application was filed on 16-07-2014 as a Morgantown, NV 26504 (US) divisional application to the application mentioned under INID code 62. (72) Inventors: • Davis, Eric Morgantown, WV 26508 (US) (54) Compositions comprising nebivolol (57) The active ingredients of the pharmaceutical composition described consist of nebivolol, one or more ACE inhibitors and one or more ARB. EP 2 808 015 A1 Printed by Jouve, 75001 PARIS (FR) EP 2 808 015 A1 Description [0001] This application is a continuation-in-part of application Ser. -
United States Patent (10) Patent No.: US 7,235,237 B2 L0scalz0 Et Al
USOO7235237B2 (12) United States Patent (10) Patent No.: US 7,235,237 B2 L0ScalZ0 et al. (45) Date of Patent: Jun. 26, 2007 (54) METHODS OF TREATING VASCULAR 5,968,983 A 10/1999 Kaesemeyer DISEASES CHARACTERIZED BY NITRC 5,973,011 A 10/1999 Noack et al. OXIDE INSUFFICIENCY 6,103,769 A 8, 2000 Kelm 6,117,872 A 9, 2000 Maxwell et al. (75) Inventors: Joseph Loscalzo, Dover, MA (US); 6,319,515 B1 1 1/2001 Hidaka et al. Joseph A. Vita, Hingham, MA (US); 6,458,797 B1 10/2002 Adams et al. Michael D. Loberg, Boston, MA (US); 2004, OO63719 A1 4/2004 Adams et al. Manuel Worcel, Boston, MA (US) FOREIGN PATENT DOCUMENTS (73) Assignee: NitroMed, Inc., Lexington, MA (US) EP O327263 A 8, 1989 (*) Notice: Subject to any disclaimer, the term of this EP O 968 713 A1 5, 1998 patent is extended or adjusted under 35 JP O905915.2 3, 1997 U.S.C. 154(b) by 492 days. WO WO95/26725 10, 1995 WO WO 98.21 193 5, 1998 (21) Appl. No.: 10/415,136 WO WO 99.00361 1, 1999 WO WO 99,66921 12/1999 (22) PCT Filed: May 2, 2001 WO WO 99,67231 12/1999 WO WO O1/35961 A 5, 2001 (86). PCT No.: PCT/USO1A14245 OTHER PUBLICATIONS S 371 (c)(1), (2), (4) Date: Apr. 25, 2003 Dupuis, Cardiovascular Drugs and Therapy, 8(3):501-507 (1994). Cohn et al. The New England Journal of Medicine, 325(5):303-310 (87) PCT Pub. -
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. -
Characterization of Explosives & Precursors
Appendix A: Project Reports ALERT Thrust R1: Characterization & Elimination of Illicit Explosives Phase 2 Year 7 Annual Report Project R1-A.1 R1-A.1: Characterization of Explosives & Precursors I. PARTICIPANTS INVOLVED FROM JULY 1, 2019 TO JUNE 30, 2020 Faculty/Staff Name Title Institution Email Jimmie Oxley Co-PI URI [email protected] Jim Smith Co-PI URI [email protected] Gerald Kagan Post-Doc URI [email protected] Graduate, Undergraduate and REU Students Name Degree Pursued Institution Month/Year of Graduation Taylor Busby PhD URI 5/2021 Lindsay McLennan PhD URI 5/2020 Robert Ichiyama PhD URI 5/2023 II. PROJECT DESCRIPTION A. Project Overview This project sought to determine the physical properties, synthesis, and destruction mechanisms of improvised explosives, often called homemade explosives (HMEs). In Year 7, we performed further characterization on erythritol tetranitrate (ETN) and on the nitro-sugars mannitol and sorbitol hexanitrate and HMTD. For ETN, we examined its synthesis and sought stable isotope signatures that might allow attribution to particular groups. For the sugars we are attempting to establish basic properties and observing different polymorphs. The existence of polymorphs was also found with HMTD. B. State of the Art and Technical Approach Stable isotope analysis is a technique capable of determining the subtle differences between the stable isotope ratios of hydrogen (2H/1H), carbon (13C/12C), nitrogen (15N/14N), oxygen (18O/16O), and, with special modifications, sulfur (34S/32S). Stable isotope analyses are important for provenance studies, where minute differences in isotope ratios can determine production location. Stable isotope ratio mass spectrometry (IRMS) has been considered as a forensic science technique for attribution that has been applied to illicit drugs, chemical weapon agents, and recently to explosives. -
Material Safety Data Sheets and Their Relevance to Customs Work
Material Safety Data Sheets and their relevance to Customs work Updated as on 18.09.2015 WCO Programme Global Shield (PGS) – E-book No.05 [Training Material for Departmental Use] E-BOOK On Material Safety Data Sheets Material Safety Data Sheets and their relevance to Customs work Note: 1. In this E-book, attempts have been made to make the officers aware about Material Safety Data Sheets and their utility at the time of handling, examination and storage of various chemicals. This will also help in proper classification of chemicals under Customs Tariff. 2. Though all efforts have been made to make this document error free, it is possible that some errors might have crept into the document. If you notice any errors, the same may be brought to the notice of the NACEN, RTI, Kanpur on the Email address: [email protected]. This may not be a perfect E-book. If you have any suggestion to improve this book, you are requested to forward the same to us. 3. This e-book is one of the several e-books dealing with different aspects of WCO Programme Global Shield (PGS). The Programme Global Shield (PGS) is a long term law enforcement initiative of WCO alongwith its partner organizations, namely, United Nations Office on Drug and Crime (UNODC), International Police Organization (INTERPOL) and member countries. This Programme is aimed at combating the illicit diversion and trafficking of high risk precursor chemicals, which are commonly used by criminal elements/terrorist organizations to make Improvised Explosive Devices (IEDs). 4. It is acknowledged here that in preparing this e-book, the WCO training material as well as material from other sources including that available freely on internet have been used.