DOCSLIB.ORG

Alphabetical Index of Substances and Articles

Total Page：16

File Type：pdf, Size：1020Kb

Download full-text PDF Read full-text
Alphabetical Index of Substances and Articles Copyright © United Nations, 2011. All rights reserved ALPHABETICAL INDEX OF SUBSTANCES AND ARTICLES Copyright © United Nations, 2011. All rights reserved Copyright © United Nations, 2011. All rights reserved NOTES TO THE INDEX 1. This index is an alphabetical list of the substances and articles which are listed in numerical order in the Dangerous Goods List in Chapter 3.2. 2. For the purpose of determining the alphabetical order the following information has been ignored even when it forms part of the proper shipping name: numbers; Greek letters; the abbreviations “sec” and “tert”; and the letters “N” (nitrogen), “n” (normal), “o” (ortho) “m” (meta), “p” (para) and “N.O.S.” (not otherwise specified). 3. The name of a substance or article in block capital letters indicates a proper shipping name. 4. The name of a substance or article in block capital letters followed by the word “see” indicates an alternative proper shipping name or part of a proper shipping name (except for PCBs). 5. An entry in lower case letters followed by the word “see” indicates that the entry is not a proper shipping name; it is a synonym. 6. Where an entry is partly in block capital letters and partly in lower case letters, the latter part is considered not to be part of the proper shipping name. 7. A proper shipping name may be used in the singular or plural, as appropriate, for the purposes of documentation and package marking. - 365 - Copyright © United Nations,INDEX 2011. All rights reserved Name and description Class UN No. Name and description Class UN No. Accumulators, electric, see 4.3 3292 Acid mixture, spent, nitrating acid, see 8 1826 8 2794 8 2795 Acraldehyde, inhibited, see 6.1 1092 8 2800 8 3028 ACRIDINE 6.1 2713 ACETAL 3 1088 ACROLEIN DIMER, STABILIZED 3 2607 ACETALDEHYDE 3 1089 ACROLEIN, STABILIZED 6.1 1092 ACETALDEHYDE AMMONIA 9 1841 ACRYLAMIDE, SOLID 6.1 2074 ACETALDEHYDE OXIME 3 2332 ACRYLAMIDE SOLUTION 6.1 3426 ACETIC ACID, GLACIAL 8 2789 ACRYLIC ACID, STABILIZED 8 2218 ACETIC ACID SOLUTION, more than 8 2790 ACRYLONITRILE, STABILIZED 3 1093 10% but not more than 80% acid, by mass Actinolite, see 9 2590 ACETIC ACID SOLUTION, more than 8 2789 Activated carbon, see 4.2 1362 80% acid, by mass Activated charcoal, see 4.2 1362 ACETIC ANHYDRIDE 8 1715 ADHESIVES containing flammable 3 1133 Acetoin, see 3 2621 liquid ACETONE 3 1090 ADIPONITRILE 6.1 2205 ACETONE CYANOHYDRIN, 6.1 1541 Aeroplane flares, see 1.1G 0420 STABILIZED 1.2G 0421 1.3G 0093 ACETONE OILS 3 1091 1.4G 0403 1.4S 0404 ACETONITRILE 3 1648 AEROSOLS 2 1950 ACETYL BROMIDE 8 1716 AGENT, BLASTING, TYPE B, see 1.5D 0331 ACETYL CHLORIDE 3 1717 AGENT, BLASTING, TYPE E, see 1.5D 0332 ACETYLENE, DISSOLVED 2.1 1001 AIR BAG INFLATORS 1.4G 0503 ACETYLENE, SOLVENT FREE 2.1 3374 9 3268 Acetylene tetrabromide, see 6.1 2504 AIR BAG MODULES 1.4G 0503 9 3268 Acetylene tetrachloride, see 6.1 1702 AIR, COMPRESSED 2.2 1002 ACETYL IODIDE 8 1898 Aircraft evacuation slides, see 9 2990 ACETYL METHYL CARBINOL 3 2621 AIRCRAFT HYDRAULIC POWER 3 3165 Acid butyl phosphate, see 8 1718 UNIT FUEL TANK (containing a mixture of anhydrous hydrazine and Acid mixture, hydrofluoric and 8 1786 methylhydrazine) (M86 fuel) sulphuric, see Aircraft survival kits, see 9 2990 Acid mixture, nitrating acid, see 8 1796 - 366 - Copyright © United Nations, 2011. All rights reserved Name and description Class UN No. Name and description Class UN No. AIR, REFRIGERATED LIQUID 2.2 1003 ALKALINE EARTH METAL 4.3 3402 AMALGAM, SOLID ALCOHOLATES SOLUTION, N.O.S., 3 3274 in alcohol ALKALINE EARTH METAL 4.3 1391 DISPERSION Alcohol, denatured, see 3 1986 1987 ALKALINE EARTH METAL 4.3 3482 DISPERSION, FLAMMABLE Alcohol, industrial, see 3 1986 ALKALOID SALTS, LIQUID, N.O.S. 6.1 3140 1987 ALKALOID SALTS, SOLID, N.O.S. 6.1 1544 ALCOHOLS, N.O.S. 3 1987 ALKALOIDS, LIQUID, N.O.S. 6.1 3140 ALCOHOLS, FLAMMABLE, TOXIC, 3 1986 N.O.S. ALKALOIDS, SOLID, N.O.S. 6.1 1544 ALCOHOLIC BEVERAGES, with 3 3065 Alkyl aluminium halides, see 4.2 3393 more than 70% alcohol by volume 3394 ALCOHOLIC BEVERAGES, with 3 3065 ALKYLPHENOLS, LIQUID, N.O.S. 8 3145 more than 24% but not more than 70% (including C2-C12 homologues) alcohol by volume ALKYLPHENOLS, SOLID, N.O.S. 8 2430 Aldehyde, see 3 1989 (including C2-C12 homologues) ALDEHYDES, N.O.S. 3 1989 ALKYLSULPHONIC ACIDS, LIQUID 8 2584 with more than 5% free sulphuric acid ALDEHYDES, FLAMMABLE, 3 1988 TOXIC, N.O.S. ALKYLSULPHONIC ACIDS, LIQUID 8 2586 with not more than 5% free sulphuric ALDOL 6.1 2839 acid ALKALI METAL ALCOHOLATES, 4.2 3206 ALKYLSULPHONIC ACIDS, SOLID 8 2583 SELF-HEATING, CORROSIVE, with more than 5% free sulphuric acid N.O.S. ALKYLSULPHONIC ACIDS, SOLID 8 2585 ALKALI METAL ALLOY, LIQUID, 4.3 1421 with not more than 5% free sulphuric N.O.S. acid ALKALI METAL AMALGAM, LIQUID 4.3 1389 ALKYLSULPHURIC ACIDS 8 2571 ALKALI METAL AMALGAM, SOLID 4.3 3401 Allene, see 2.1 2200 ALKALI METAL AMIDES 4.3 1390 ALLYL ACETATE 3 2333 ALKALI METAL DISPERSION 4.3 1391 ALLYL ALCOHOL 6.1 1098 ALKALI METAL DISPERSION, 4.3 3482 ALLYLAMINE 6.1 2334 FLAMMABLE ALLYL BROMIDE 3 1099 Alkaline corrosive battery fluid, see 8 2797 ALLYL CHLORIDE 3 1100 ALKALINE EARTH METAL 4.2 3205 ALCOHOLATES, N.O.S. Allyl chlorocarbonate, see 6.1 1722 ALKALINE EARTH METAL ALLOY, 4.3 1393 ALLYL CHLOROFORMATE 6.1 1722 N.O.S. ALKALINE EARTH METAL 4.3 1392 ALLYL ETHYL ETHER 3 2335 AMALGAM, LIQUID - 367 - Copyright © United Nations, 2011. All rights reserved Name and description Class UN No. Name and description Class UN No. ALLYL FORMATE 3 2336 ALUMINIUM SILICON POWDER, 4.3 1398 UNCOATED ALLYL GLYCIDYL ETHER 3 2219 ALUMINIUM SMELTING 4.3 3170 ALLYL IODIDE 3 1723 BY-PRODUCTS ALLYL ISOTHIOCYANATE, 6.1 1545 Amatols, see 1.1D 0082 STABILIZED AMINES, FLAMMABLE, 3 2733 ALLYLTRICHLOROSILANE, 8 1724 CORROSIVE, N.O.S. STABILIZED AMINES, LIQUID, CORROSIVE, 8 2735 Aluminium alkyl halides, liquid, see 4.2 3394 N.O.S. Aluminium alkyl halides, solid, see 4.2 3393 AMINES, LIQUID, CORROSIVE, 8 2734 FLAMMABLE, N.O.S. Aluminium alkyl hydrides, see 4.2 3394 AMINES, SOLID, CORROSIVE, 8 3259 Aluminium alkyls, see 4.2 3394 N.O.S. ALUMINIUM BOROHYDRIDE 4.2 2870 Aminobenzene, see 6.1 1547 ALUMINIUM BOROHYDRIDE IN 4.2 2870 2-Aminobenzotrifluoruride, see 6.1 2942 DEVICES 3-Aminobenzotrifluoruride, see 6.1 2948 ALUMINIUM BROMIDE, 8 1725 ANHYDROUS Aminobutane, see 3 1125 ALUMINIUM BROMIDE SOLUTION 8 2580 2-AMINO-4-CHLOROPHENOL 6.1 2673 ALUMINIUM CARBIDE 4.3 1394 2-AMINO-5-DIETHYL- 6.1 2946 AMINOPENTANE ALUMINIUM CHLORIDE, 8 1726 ANHYDROUS 2-AMINO-4,6-DINITROPHENOL, 4.1 3317 WETTED with not less than 20% ALUMINIUM CHLORIDE 8 2581 water, by mass SOLUTION 2-(2-AMINOETHOXY)ETHANOL 8 3055 Aluminium dross, see 4.3 3170 N-AMINOETHYLPIPERAZINE 8 2815 ALUMINIUM FERROSILICON 4.3 1395 POWDER 1-Amino-2-nitrobenzene, see 6.1 1661 ALUMINIUM HYDRIDE 4.3 2463 1-Amino-3-nitrobenzene, see 6.1 1661 ALUMINIUM NITRATE 5.1 1438 1-Amino-4-nitrobenzene, see 6.1 1661 ALUMINIUM PHOSPHIDE 4.3 1397 AMINOPHENOLS (o-, m-, p-) 6.1 2512 ALUMINIUM PHOSPHIDE 6.1 3048 AMINOPYRIDINES (o-, m-, p-) 6.1 2671 PESTICIDE AMMONIA, ANHYDROUS 2.3 1005 ALUMINIUM POWDER, COATED 4.1 1309 AMMONIA SOLUTION relative 8 2672 ALUMINIUM POWDER, UNCOATED 4.3 1396 density between 0.880 and 0.957 at 15 °C in water, with more than 10% ALUMINIUM REMELTING 4.3 3170 but not more than 35% ammonia BY-PRODUCTS ALUMINIUM RESINATE 4.1 2715 - 368 - Copyright © United Nations, 2011. All rights reserved Name and description Class UN No. Name and description Class UN No. AMMONIA SOLUTION, relative 2.2 2073 AMMONIUM NITRATE GEL, 5.1 3375 density less than 0.880 at 15 °C in intermediate for blasting explosives water, with more than 35% but not more than 50% ammonia AMMONIUM NITRATE, LIQUID 5.1 2426 (hot concentrated solution) AMMONIA SOLUTION, relative 2.3 3318 density less than 0.880 at 15 °C in AMMONIUM NITRATE 5.1 3375 water, with more than 50% ammonia SUSPENSION, intermediate for blasting explosives AMMONIUM ARSENATE 6.1 1546 AMMONIUM NITRATE with more 1.1D 0222 Ammonium bichromate, see 5.1 1439 than 0.2% combustible substances, including any organic substance Ammonium bifluoride solid, see 8 1727 calculated as carbon, to the exclusion of any other added substance Ammonium bifluoride solution, see 8 2817 AMMONIUM NITRATE, with not 5.1 1942 Ammonium bisulphate, see 8 2506 more than 0.2% total combustible material, including any organic Ammonium bisulphite solution, see 8 2693 substance, calculated as carbon to the exclusion of any other added substance AMMONIUM DICHROMATE 5.1 1439 AMMONIUM PERCHLORATE 1.1D 0402 AMMONIUM DINITRO-o- 6.1 1843 5.1 1442 CRESOLATE, SOLID Ammonium permanganate, see 5.1 1482 AMMONIUM DINITRO-o- 6.1 3424 CRESOLATE, SOLUTION AMMONIUM PERSULPHATE 5.1 1444 AMMONIUM FLUORIDE 6.1 2505 AMMONIUM PICRATE dry or wetted 1.1D 0004 with less than 10% water, by mass AMMONIUM FLUOROSILICATE 6.1 2854 AMMONIUM PICRATE, WETTED 4.1 1310 Ammonium hexafluorosilicate, see 6.1 2854 with not less than 10% water, by mass AMMONIUM HYDROGEN- 8 1727 AMMONIUM POLYSULPHIDE 8 2818 DIFLUORIDE, SOLID SOLUTION AMMONIUM HYDROGEN- 8 2817 AMMONIUM POLYVANADATE 6.1 2861 DIFLUORIDE SOLUTION Ammonium silicofluoride, see 6.1 2854 AMMONIUM HYDROGEN 8 2506 SULPHATE AMMONIUM SULPHIDE SOLUTION 8 2683 Ammonium hydrosulphide solution 8 2683 Ammunition, blank, see 1.1C 0326 (treat as ammonium sulphide solution), 1.2C 0413 see 1.3C 0327 1.4C 0338 AMMONIUM METAVANADATE 6.1 2859 1.4S 0014 AMMONIUM NITRATE BASED 5.1 2067 Ammunition, fixed ) see 1.1E 0006 FERTILIZER 9 2071 Ammunition, semi-fixed ) 1.1F 0005 Ammunition, separate loading, ) 1.2E 0321 AMMONIUM NITRATE EMULSION, 5.1 3375 1.2F 0007 intermediate for blasting explosives 1.4E 0412 1.4F 0348 Ammonium nitrate explosive, see 1.1D 0082 1.5D 0331 AMMUNITION, ILLUMINATING 1.2G 0171 with or without burster, expelling 1.3G 0254 charge or propelling charge 1.4G 0297 - 369 - Copyright © United Nations, 2011.
Load more

Recommended publications
  • 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.
    [Show full text]
  • Chloroplatinic Acid Hydrate
    Chloroplatinic acid hydrate sc-239532 Material Safety Data Sheet Hazard Alert Code Key: EXTREME HIGH MODERATE LOW Section 1 - CHEMICAL PRODUCT AND COMPANY IDENTIFICATION PRODUCT NAME Chloroplatinic acid hydrate STATEMENT OF HAZARDOUS NATURE CONSIDERED A HAZARDOUS SUBSTANCE ACCORDING TO OSHA 29 CFR 1910.1200. NFPA FLAMMABILITY0 HEALTH3 HAZARD INSTABILITY0 SUPPLIER Santa Cruz Biotechnology, Inc. 2145 Delaware Avenue Santa Cruz, California 95060 800.457.3801 or 831.457.3800 EMERGENCY: ChemWatch Within the US & Canada: 877-715-9305 Outside the US & Canada: +800 2436 2255 (1-800-CHEMCALL) or call +613 9573 3112 SYNONYMS Cl6-H2-Pt, H2PtCl6, "chloroplatinic (IV) acid", "chloroplatinic acid", "chlorplatinic acid", "dihydrogen hexachloroplatinate", "hydrogen hexachlorplatinate", "platinum chloride", "acid platinic chloride" Section 2 - HAZARDS IDENTIFICATION CHEMWATCH HAZARD RATINGS Min Max Flammability: 0 Toxicity: 3 Body Contact: 3 Min/Nil=0 Low=1 Reactivity: 0 Moderate=2 High=3 Chronic: 2 Extreme=4 CANADIAN WHMIS SYMBOLS 1 of 9 EMERGENCY OVERVIEW RISK Toxic if swallowed. Causes burns. Risk of serious damage to eyes. May cause SENSITISATION by inhalation and skin contact. POTENTIAL HEALTH EFFECTS ACUTE HEALTH EFFECTS SWALLOWED ! Toxic effects may result from the accidental ingestion of the material; animal experiments indicate that ingestion of less than 40 gram may be fatal or may produce serious damage to the health of the individual. ! The material can produce chemical burns within the oral cavity and gastrointestinal tract following ingestion. ! Ingestion of acidic corrosives may produce burns around and in the mouth. the throat and esophagus. EYE ! The material can produce chemical burns to the eye following direct contact. Vapors or mists may be extremely irritating.
    [Show full text]
  • United States Patent (19) 11 Patent Number: 4,820,674 Shiozawa Et Al
    United States Patent (19) 11 Patent Number: 4,820,674 Shiozawa et al. 45) Date of Patent: Apr. 11, 1989 54 PROCESS FOR PREPARING A 58) Field of Search ....................... 502/169, 172, 230; HYDROSLYLATION CATALYST 556/479, 136; 549/206, 211 75 Inventors: Kouji Shiozawa, Saitama; Yoshiharu (56) References Cited Okumura, Tokyo; Chihiro Imai, U.S. PATENT DOCUMENTS Kanagawa; Nobukazu Okamoto, 3,220,972 11/1965 Lamoreaux ......................... 502/169 Saitama, all of Japan 3,624,119 11/1971 Rothe.................................. 502/169 73) Assignee: Toa Nenryo Kogyo Kabushiki Kaisha, 3,814,731 6/1974 Nitzsche .............................. 502/169 Tokyo, Japan Primary Examiner-Patrick P. Garvin Assistant Examiner-Elizabeth Irzinski 21 Appl. No.: 149,092 Attorney, Agent, or Firm-Wenderoth, Lind and Ponack 22 Filed: Jan. 27, 1988 57 ABSTRACT A process for preparing a hydrosilylation catalyst by 30 Foreign Application Priority Data dissolving chloroplatinic acid H2PtCl6 in a cyclic ether or cyclic ester containing at least 3 carbon atoms, and Jan. 29, 1987 JP Japan .................................. 62-18916 maintaining the resulting solution at a temperature of at (51 Int. Cl. .............................................. B01J 31/00 least 3O C. 52 U.S. Cl. .................................... 502/169; 502/172; 502/230 4. Claims, No Drawings 4,820,674 1. 2 the resulting solution at a temperature of at least 30 C., PROCESS FOR PREPARING A preferably from 50° to 120° C. HYDROSILYLATION CATALYST DETAILED DESCRIPTION OF THE BACKGROUND OF THE INVENTION INVENTION This invention relates to a process for preparing a A process for preparing a hydrosilylation catalyst hydrosilylation catalyst which is preferably used in according to the present invention will be fully de synthesizing a silane coupling agent and, more particu scribed hereinafter.
    [Show full text]
  • Method for the Preparation of Cyclopentyl Trichlorosilane
    Europaisches Patentamt (19) European Patent Office Office europeenpeen des brevets EP 0 460 589 B1 (12) EUROPEAN PATENT SPECIFICATION (45) Date of publication and mention (51) Int Cl.e: C07F 7/14 of the grant of the patent: 04.11.1998 Bulletin 1998/45 (21) Application number: 91109082.7 (22) Date of filing: 04.06.1991 (54) Method for the preparation of cyclopentyl Trichlorosilane Verfahren zur Herstellung von Cyclopentyl-trichlorosilan Procede de preparation de cyclopentyl trichlorosilane (84) Designated Contracting States: (74) Representative: DE FR GB IT Luderschmidt, Schiiler & Partner GbR Patentanwalte, (30) Priority: 07.06.1990 JP 149338/90 Postfach 3929 65029 Wiesbaden (DE) (43) Date of publication of application: 11.12.1991 Bulletin 1991/50 (56) References cited: EP-A- 0 278 863 DE-A- 1 941 411 (73) Proprietor: SHIN-ETSU CHEMICAL CO., LTD. GB-A-2 013 207 Chiyoda-ku Tokyo (JP) • CHEMICAL ABSTRACTS vol. 89, no. 17, 23 (72) Inventors: October 1 978, page 61 9, abstract no. 1 46975f , • Shinohara, Toshio Columbus, Ohio, US; R.A. BENKESER: Takasaki-shi, Gunma-ken (JP) "Chloroplatinic acid catalyzed additions of • Iwabuchi, Motoaki silanes to isoprene" Annaka-shi, Gunma-ken (JP) DO O) 00 CO ^- Note: Within nine months from the publication of the mention of the grant of the European patent, any person may give notice the Patent Office of the Notice of shall be filed in o to European opposition to European patent granted. opposition a written reasoned statement. It shall not be deemed to have been filed until the opposition fee has been paid. (Art. a.
    [Show full text]
  • Approved and Prohibited Fireworks Chemicals
    Version 2 - Updated November 5, 2019 Approved and Prohibited Fireworks Chemicals (NOTE: Restriction Column is added to group restrictions together) Chemical Formula Typical Use Restrictions Alloprene (Chlorinated Rubber) Not Required Color Intensifier Ok for use in a break charge and other Aluminum (> 53 microns) Al Fuel compositions including report compositions Aluminum (≤ 53 microns) Al Fuel Report composition only Not to exceed 5% of formulation Ammonium Dichromate (NH ) Cr O Oxygen Donor / Colored Ash 4 2 2 7 Prohibited if mixed with a Chlorate Ammonium Perchlorate NH4ClO4 Oxygen Donor Prohibited if mixed with a Chlorate Anthracene C14H10 Fuel Antimony Sb Fuel Antimony Sulfide: Antimonous Sulfide or Antimony Trisulfide Sb2S3 Fuel Antimony Trioxide Sb2O3 Oxygen Donor Barium Carbonate BaCO3 Color Agent 1) In smoke formulations an equal or greater weight of bicarbonates or carbonates is required; 2) In all other devices the total chemical Barium Chlorate Ba(ClO ) Oxygen Donor / Color Agent 3 2 composition cannot exceed 4 grams of which no more than 15 percent can be chlorate salts; 3) Permitted in firecrackers, party poppers and booby traps. Barium Nitrate Ba(NO3)2 Oxygen Donor / Color Agent Barium Oxalate BaC2O4 Color Agent Barium Phthalate Ba(C8H5O4)2 Whistle / Color Agent Barium Sulfate BaSO4 Oxygen Donor / Color Agent Benzoic Acid Potassium Salt (Potassium Benzoate) KC6H5CO2 or KC7H5O2 Whistle / Fuel Benzoic Acid Sodium Salt (Sodium Benzoate) NaC6H5CO2 or NaC7H5O2 Whistle / Fuel Bismuth Oxide or Bismuth Trioxide Bi2O3 Oxygen Donor
    [Show full text]
  • Material Safety Data Sheet Chloroplatinic Acid Hydrate ACC# 04841 Section 1 - Chemical Product and Company Identification
    Material Safety Data Sheet Chloroplatinic acid hydrate ACC# 04841 Section 1 - Chemical Product and Company Identification MSDS Name: Chloroplatinic acid hydrate Catalog Numbers: AC195370000, AC195370010, AC195370050, AC363590000, AC363590010, AC405010000, AC405010010, AC405010050, P154-1, P154-10 Synonyms: Dihydrogen hexachloroplatinate hydrate; Platinate(2-), hexachloro-, dihydrogen, hydrate; Platinic chloride hydrate; Hydrogen hexachloroplatinate(IV) hydrate. Company Identification: Fisher Scientific 1 Reagent Lane Fair Lawn, NJ 07410 For information, call: 201-796-7100 Emergency Number: 201-796-7100 For CHEMTREC assistance, call: 800-424-9300 For International CHEMTREC assistance, call: 703-527-3887 Section 2 - Composition, Information on Ingredients CAS# Chemical Name Percent EINECS/ELINCS 16941-12-1 Chloroplatinic acid anhydrous 99 241-010-7 18497-13-7 Chloroplatinic acid hexahydrate ref unlisted 26023-84-7 Platinate(2-), hexachloro-, dihydrogen, hydrate ref unlisted Section 3 - Hazards Identification EMERGENCY OVERVIEW Appearance: orange-brown powder and chunks. Danger! Causes eye and skin burns. Causes digestive and respiratory tract burns. May cause severe allergic respiratory reaction. Harmful if swallowed. May cause allergic skin reaction. Target Organs: Lungs, eyes, skin, mucous membranes. Potential Health Effects Eye: Causes eye burns. Skin: May cause skin sensitization, an allergic reaction, which becomes evident upon re-exposure to this material. May cause severe irritation and possible burns. Ingestion: Harmful if swallowed. May cause severe gastrointestinal tract irritation with nausea, vomiting and possible burns. Inhalation: May cause allergic respiratory reaction. May cause severe respiratory tract irritation. May cause asthma and shortness of breath. Chronic: Repeated exposure may cause allergic respiratory reaction (asthma). Exposure may cause platinosis, a morbid condition resulting from exposure to soluble platinum salts, with involvement of the upper respiratory tract and allergic manifestations of the skin.
    [Show full text]
  • 2020 Emergency Response Guidebook
    2020 A guidebook intended for use by first responders A guidebook intended for use by first responders during the initial phase of a transportation incident during the initial phase of a transportation incident involving hazardous materials/dangerous goods involving hazardous materials/dangerous goods EMERGENCY RESPONSE GUIDEBOOK THIS DOCUMENT SHOULD NOT BE USED TO DETERMINE COMPLIANCE WITH THE HAZARDOUS MATERIALS/ DANGEROUS GOODS REGULATIONS OR 2020 TO CREATE WORKER SAFETY DOCUMENTS EMERGENCY RESPONSE FOR SPECIFIC CHEMICALS GUIDEBOOK NOT FOR SALE This document is intended for distribution free of charge to Public Safety Organizations by the US Department of Transportation and Transport Canada. This copy may not be resold by commercial distributors. https://www.phmsa.dot.gov/hazmat https://www.tc.gc.ca/TDG http://www.sct.gob.mx SHIPPING PAPERS (DOCUMENTS) 24-HOUR EMERGENCY RESPONSE TELEPHONE NUMBERS For the purpose of this guidebook, shipping documents and shipping papers are synonymous. CANADA Shipping papers provide vital information regarding the hazardous materials/dangerous goods to 1. CANUTEC initiate protective actions. A consolidated version of the information found on shipping papers may 1-888-CANUTEC (226-8832) or 613-996-6666 * be found as follows: *666 (STAR 666) cellular (in Canada only) • Road – kept in the cab of a motor vehicle • Rail – kept in possession of a crew member UNITED STATES • Aviation – kept in possession of the pilot or aircraft employees • Marine – kept in a holder on the bridge of a vessel 1. CHEMTREC 1-800-424-9300 Information provided: (in the U.S., Canada and the U.S. Virgin Islands) • 4-digit identification number, UN or NA (go to yellow pages) For calls originating elsewhere: 703-527-3887 * • Proper shipping name (go to blue pages) • Hazard class or division number of material 2.
    [Show full text]
  • Electrochemical Preparation of Strontium Perchlorate
    Korean J. Chem. Eng., 26(5), 1246-1251 (2009) DOI: 10.2478/s11814-009-0224-5 RAPID COMMUNICATION Optimization of the process parameters for an electrochemical preparation of strontium perchlorate Subramanyan Vasudevan† Central Electrochemical Research Institute (CSIR), Karaikudi 630006, India (Received 14 January 2009 • accepted 10 March 2009) Abstract−The electrochemical preparation of strontium perchlorate, Sr(ClO4)2, from strontium chlorate employing platinum anode and a rotating stainless steel cathode is described. The effect of electrolyte concentration, current den- sity, pH and temperature of the electrolyte and cathode rotation on current efficiency for the preparation of strontium perchlorate was studied. A maximum current efficiency of 42% was achieved corresponding to an energy consumption of 6.1 kWh. kg−1. Key words: Electorchemical, Oxidation, Strontium Perchlorate, Rotating Cathode INTRODUCTION Therefore, the main objective of this study is to prepare stron- tium perchlorate from strontium chlorate, by electrochemical method, The preparation of alkali metal perchlorates by electrolysis of using platinum and rotating stainless steel as anode and cathode, the corresponding chlorates has been studied by various authors respectively. To optimize the parametric conditions, the various pa- [1]. Schumacher [2] reported other methods for manufacturing of rameters like effect of electrolyte concentration, pH and tempera- perchlorates from different raw materials. The mechanism, kinetic ture, current density and cathode rotation on current efficiency was in- aspects and electrode materials for perchlorate formation were dealt vestigated. Strontium perchlorate is used as secondary injection thrust with within the literature [3-7]. After understanding the mechanism vector control (SITVC) of the first stage satellite launch vehicles. of perchlorate formation, attempts were made to study the different 1.
    [Show full text]
  • Wo 2010/117346 A2
    (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 14 October 2010 (14.10.2010) WO 2010/117346 A2 (51) International Patent Classification: AO, AT, AU, AZ, BA, BB, BG, BH, BR, BW, BY, BZ, A61K 31/593 (2006.01) CA, CH, CL, CN, CO, CR, CU, CZ, DE, DK, DM, DO, DZ, EC, EE, EG, ES, FI, GB, GD, GE, GH, GM, GT, (21) International Application Number: HN, HR, HU, ID, IL, IN, IS, JP, KE, KG, KM, KN, KP, PCT/TR20 10/000081 KR, KZ, LA, LC, LK, LR, LS, LT, LU, LY, MA, MD, (22) International Filing Date: ME, MG, MK, MN, MW, MX, MY, MZ, NA, NG, NI, 9 April 2010 (09.04.2010) NO, NZ, OM, PE, PG, PH, PL, PT, RO, RS, RU, SC, SD, SE, SG, SK, SL, SM, ST, SV, SY, TH, TJ, TM, TN, TR, (25) Filing Language: English TT, TZ, UA, UG, US, UZ, VC, VN, ZA, ZM, ZW. (26) Publication Language: English (84) Designated States (unless otherwise indicated, for every (30) Priority Data: kind of regional protection available): ARIPO (BW, GH, 2009/02817 10 April 2009 (10.04.2009) TR GM, KE, LR, LS, MW, MZ, NA, SD, SL, SZ, TZ, UG, ZM, ZW), Eurasian (AM, AZ, BY, KG, KZ, MD, RU, TJ, (72) Inventor; and TM), European (AT, BE, BG, CH, CY, CZ, DE, DK, EE, (71) Applicant : BILGIC, Mahmut [TR/TR]; Tozkoparan ES, FI, FR, GB, GR, HR, HU, IE, IS, IT, LT, LU, LV, Mah.
    [Show full text]
  • United States Patent Office Patented Oct
    3,698,939 United States Patent Office Patented Oct. 17, 1972 2 It is a still further object of this invention to provide 3,698,939 an electroless method for depositing adherent, dense and METHOD AND COMPOSITION OF continuous layers of platinum directly over metals more PLATINUM PLATING Frank H. Leaman, 1613 N. Harrison St. noble than copper and metal alloys more noble than York, Pa. 17402 copper to a predetermined thickness. No Drawing. Filed July 9, 1970, Ser. No. 53,639 It is a further object of this invention to provide an Int, C. C23c 3/02 electroless method for depositing adherent, dense and con U.S. C. 117-130 11 Claims tinuous layers of platinum directly over various non-con ductive materials which have been plated by electroless O techniques. ABSTRACT OF THE DISCLOSURE It is a further object of this invention to employ hy A method is provided for the electroless platinum drazine or salts and derivatives of hydrazine, such as hy plating onto metals and alloys of metals more noble than drazine sulfate, to reduce chloroplatinate complexed in copper and onto non-conductive materials by the chemi ammoniacal aqueous solutions at a low temperature so as 5 to obtain a dense metallic platinum deposit over sub cal reduction of platinum from an aqueous alkaline solu Strates. tion containing a chloroplatinate complex. Still further objects and advantages of the present in e-maseaux-saman vention will become apparent from the following more This invention relates to a process for electroless detailed description of the invention. plating of platinum on various substrates which heretofore 20 The electroless plating composition used in the present have not successfully been electrolessly platinum plated.
    [Show full text]
  • Synthesis and Characterization of Nitric Oxide-Releasing Silica Materials for Sensing Applications
    SYNTHESIS AND CHARACTERIZATION OF NITRIC OXIDE-RELEASING SILICA MATERIALS FOR SENSING APPLICATIONS by Jae Ho Shin A dissertation submitted to the faculty of the University of North Carolina at Chapel Hill in partial fulfillment of the requirements for the degree of Doctor of Philosophy in the Department of Chemistry (Analytical Chemistry). Chapel Hill 2006 Approved by Professor Mark H. Schoenfisch Professor Royce W. Murray Professor Malcolm D. E. Forbes Professor Jeffrey S. Johnson Professor Wei You ABSTRACT JAE HO SHIN: Synthesis and Characterization of Nitric Oxide-Releasing Silica Materials for Sensing Applications (Under the direction of Professor Mark H. Schoenfisch) Nitric oxide (NO), a free radical endogenously synthesized in the human body, regulates a range of biological processes in the cardiovascular, genitourinary, respiratory, and nervous systems. With the discovery of NO as a potent inhibitor of platelet activation and its identification as an antibacterial agent, the utility of NO has been expanded to developing more biocompatible materials that resist to biofouling. My research has focused on the development of NO-releasing glucose biosensors via xerogel/polyurethane hybrid membranes that release NO in a controlled fashion. This new class of glucose biosensors was characterized by both adequate analytical response to glucose and improved bacterial adhesion resistance at NO fluxes ≥ 5 pmol·cm-2·s-1 for 20 h. To further elucidate the complex and wide ranging roles of NO in physiology, an amperometric xerogel-based NO microsensor was fabricated. Several silicon-based NO sensor membranes were synthesized by doping alkyl/amino-alkoxysilane-based xerogels with Nafion. The performance of xerogel-based NO sensors was then evaluated to identify the optimum xerogel composition that maximized NO permeability and provided sufficient selectivity for NO.
    [Show full text]
  • Platinum-Catalyzed Hydrosilylation in Polymer Chemistry
    polymers Review Platinum-Catalyzed Hydrosilylation in Polymer Chemistry Ruslan Yu. Lukin 1,2,*, Aidar M. Kuchkaev 1,2, Aleksandr V. Sukhov 1,2, Giyjaz E. Bekmukhamedov 1,2 and Dmitry G. Yakhvarov 1,2,* 1 Alexander Butlerov Institute of Chemistry, Kazan Federal University, 420008 Kazan, Russia; [email protected] (A.M.K.); alex.suhoff@rambler.ru (A.V.S.); [email protected] (G.E.B.) 2 Arbuzov Institute of Organic and Physical Chemistry, FRC Kazan Scientific Center of the Russian Academy of Sciences, 420088 Kazan, Russia * Correspondence: [email protected] (R.Y.L.); [email protected] (D.G.Y.); Tel.: +7-843-2337416 (R.Y.L. & D.G.Y.); Fax: +7-843-2732253 (R.Y.L. & D.G.Y.) Received: 20 July 2020; Accepted: 15 September 2020; Published: 23 September 2020 Abstract: This paper addresses a review of platinum-based hydrosilylation catalysts. The main field of application of these catalysts is the curing of silicone polymers. Since the 1960s, this area has developed rapidly in connection with the emergence of new polymer compositions and new areas of application. Here we describe general mechanisms of the catalyst activity and the structural effects of the ligands on activity and stability of the catalysts together with the methods for their synthesis. Keywords: silicone polymers; hydrosilylation; organometallic catalysts; platinum complexes 1. Introduction The hydrosilylation reaction (also referred to as hydrosilation) is widely used in the organosilicon industry. This reaction represents the addition of silicon-hydrogen bonds (Si–H) via an unsaturated carbon–carbon double bond (C=C), carbon–oxygen, and carbon–nitrogen double bonds.
    [Show full text]