DOCSLIB.ORG

List of Dielectric Constants

Total Page：16

File Type：pdf, Size：1020Kb

Download full-text PDF Read full-text
List of Dielectric Constants List of Dielectric Constants The following list of dielectric constants is based on approximate values for the substance listed in its natural state. These values are for informational purposes only. The list should be used as a guide to help the user find the appropriate instrument type, but are not guaranteed to be descriptive of every customer's process. Information may be changed at any time without notice. Substance DK-Value Substance DK-Value A Caprylic acid 2.5 Acetal 3.8 Carbazole 1.3 Acetaldehyde 15 Carbon black 18.8 Acetamide 59.2 Carbon disulphide 2.6 Acetic acid 6.2 Carbon tetrachloride 2.3 Acetoacetic acid ethyl ester 15 Carbonylcyanid 10.7 Acetone 21.5 Caustic potash 3.3 Acetophenone 18 Cellit 1.6 Acetyl bromide 16.2 Cellulose 1.2 Acetyl chloride 15.9 Cement 2.2 Acetylacetone 23 Cement asbestos 3.2 Acetylene dibromide 7.2 Ceramic compound 17 Acetylene tetrabromide 5.6 Cetyl alcohol (60°C) 3.6 Aconite acid ester 6.3 Chaff 1.5 Activated carbon 12 Chalk 2.1 Adipic Acid 1.8 Chamotte 1.8 Aerosile 1 Charcoal 1.3 Aether 4 Chloorhydrin 31 Allyl alcohol 20.6 Chlor benzene 5.7 Allyl chloride 8.2 Chlor. fluid 2.1 Allyl iodide 6.1 Chloral 6.7 Alum 4.2 Chlorinated lime 2.3 Aluminium bromide 3.4 Chloroacetic acid 33.4 Aluminium foil 10.8 Chloroform (trichlormethane) 4.8 Aluminium hydroxide 2.5 Chocolate powder 2 Aluminium splinters 7.3 Clay 2.3 Aluminium sulfate 2.6 Coal dust 2.5 Ammonia 15 Coal. 15 % moisture 4 Ammonia salt 4.3 Coconut oil (refined) 2.9 Ammonia solution (25%) 31.6 Coffee beans 1.5 Amyl amine 4.5 Coke 3 Aniline 7 Cola essence 17.3 Animal feed grist 2.4 Concentrated feed 3.2 Anisealdehyde 22.3 Copper ore 5.6 Anisole 4.5 Cork powder 1.7 Anthracite/hard coal 3.2 Corn 3.6 Antimony hydride 1.8 Corn grist 2.1 Argon 1.5 Corn starch sirup 18.4 Arsine 2.1 Cotton fibre flour 3.2 Arsole 2.3 Cream (skin) 19 Asbestos 10 Cresol 11 Ascorbic acid (vitamin C) 2.1 Cresol resin 18.3 Azelaic acid diethylester 5 Crystal sugar 2 Azoxybenzene 5.2 Cullet 2 B Cuminaldehyde 10.7 Basalt 2.5 Cyanogen 2.5 Bauxite 2.5 D Beer brew 25 Decalin 2.1 Beets cuttings 7.3 Degalan 3.1 Beets seeds 3.5 Desmodur 10 Bentonite 8.1 Diacetone alcohol 18.2 Benzal chloride 6.9 Diamylether 3 Benzaldehyd 17.6 Diatomaceous earth 1.4 Benzene 2.3 Dibenzofuran (100°C) 3 Benzene. heavy 3.2 Dibenzyl (60°C) 2.5 Benzil (80°C) 10 Diesel Fuel 2.1 Benzine 2 Diethyl carbonate 2.8 Benzyl alcohol 13.5 Diethylamine 3.8 Benzyl chloride 7 Dimethylether (methyl ether) 5 Benzyl amine 4.6 Diofan 32 Bitumen 2.8 Dioxane 2 Black liquor 32 Diphenyl 2.5 Bone fat 2.7 Dry yeast 2 Bonemeal 1.7 E Bore oil emulsion 25 Emulphor 4 Bornylacetat 4.6 Epichlorhydrin 23 Bromine 3.1 Ethanol (ethyl alkohol) 16.2 Butanoic acid 3 Ethayl acetate 6 C Ethyl benzene 2.4 Cacao beans 1.8 Ethyl benzoate 6 Calcium fluoride 2.5 Ethyl mercaptan 6.9 Camphene 2.3 Ethylamine 6.9 Caproic acid 2.6 Ethylene chlorhydrin 25 Substance DK-Value Substance DK-Value Ethylene chloride 10.6 Isoamyl bromide 6 Ethylenediamine 15 Isoamyl chloride 6.1 Etylene oxide 13.9 Isoamyl ether 2.8 F Isoamyl iodide 5.6 Fat coal 3.4 Isobutanoic acid 2.6 Fatty acid 1.7 Isobutyl alcohol 18.1 Fenchone 12.8 Isobutyl amine 4.4 Ferrite pellets 21 Isobutyl benzene 2.3 Ferrosilicon 10 Isobutyl bromide 7.2 Ferrozell 18.3 Isobutyl chloride 6.5 Fertiliser 4.3 Isobutyl cyanide 18 Fiber glass powder 1.1 Isobutyl iodide 6.5 Fish oil 2.6 Isobutyl nitrate 11.7 Flax pellets 1.4 Isobutyl silane 2.5 Flour 2.5 Isocyanate 6.1 Fluorbenzene 6.4 Isoprene 2.1 Fluorine 1.5 Isopropanol 18 Fly ash 3.3 Isoquinoline 10.7 Foam flakes 1.1 Isosafrol 3.3 Formamide 109 K Formic acid 57.9 Ketchup 24 Furan 3 L Furfurol 41.7 Lanolin 4.2 G Lard (80°C) 2.1 Gas 2 Latex 24 Germanium tetrachloride 2.4 Laughing gas 1.5 Glass granulate 4 Lauric acid ethyl ester 3.4 Glucose (50%) 30 Lime 2 Glue 2 Linoleic acid 2.7 Glycerol 13.2 M Glycerol water 37 Malic acid diethylester 10 Glycol 37 Malt 2.7 Glysantin 25 Mandelic acid nitril 18 Grain grist 3 Marble stones small (2-3 mm) 2.5 Grain of mustard seed 3.6 Meat and bone meal 1.9 Grain of soy 2.9 Meat and bone meal 2.2 Granuform 4 Menthol 4 Gravel 2.6 Mercury diethyl 2.1 Green vitriol 32.4 Mesityl oxide 15 Guaiacol 11 Metal powder 6 Guano 2.5 Methanol (methyl alkohol) 33 Gypsum 1.8 Methyl acetate 8 H Methyl cellulose 3 Hazels 2 Methyl iodide 7.1 Heating oil 2.1 Methyl nitrate 23.5 Heavy fuel oil 2.2 Methylene bromide 7 Helium 1.1 Methylene chloride 9 Heptanal 9.1 Methylene chloride 9.1 Heptane 1.9 Metylene iodide 5.3 Heptanoic acid 2.6 Mice feed 2.3 Heptene 2.1 Molasses 31.3 Hexachlorobutadiene 2.6 Mono chlormethane 9.8 Hexane 1.9 Morpholine 7.3 Hexanol 12.5 Mustard 24 Hexene 2.1 N Hibiscus 2.8 Naphtalene 2.5 Honey 24 Naphthenic acid 2.6 Hot glue 2.3 Nitric acid (98%) 19 Hydrazine 58 Nitro phoska 5.4 Hydrochloric acid 5 Nitro varnish 5.2 Hydrogen 1.2 Nitrobenzene 35 Hydrogen cyanide 158 Nitroethane 29 Hydrogen Fluoride 83.6 Nitroglycerin 19.3 Hydrogen iodide 2.9 Nitroglycol 28.3 Hydrogen peroxide 84.2 Nitromethane 39 Hydrogen sulfide 6 Nitrosyl bromide 15.2 I Nitrosyl chloride 19 Ice cream 16.5 O Imidazole. pure 23 Oat 4.9 Iodine 11.1 Octane 2 Iodobenzene 4.6 Octene 2.1 Iron(III)oxide red 1.9 Octyl bromide 5 Isoamyl acetate 4.8 Oil 2 Isoamyl alcohol 15.6 Oleic acid 2.5 Substance DK-Value Substance DK-Value Oxalo ethyl acetate 6 Silicone oil 2.7 Oxygen 1.5 Silicone rubber 2.9 P Skim milk powder 2.3 Palm nut/kernel/seed 2.8 Soap flakes 9.2 Palm seed oil 1.8 Soap pellets 3.5 Palm tree nut 2.2 Soda 3 Palmitic acid 2.3 Sodium chloride 23 Paper scraps 1.2 Sodium methylate 1.5 Paraffin 1.6 Sodium perborate 2.2 Paraldehyde 15.1 Sodium peroxide 2.7 Pasta 1.9 Sodium silicate 16 Peanuts, dried 3.1 Sodium sulfate 2.7 Peanut expeller 2.4 Soft soap 32 Pelargon 2.8 Solvent 18 Penta borane 21 Soy flour 4.5 Penta chlortoluene 4.8 Splints 1.1 Penta ethyl chloride 3.8 Stearic acid 2.3 Pentanal 11.8 Styrene 2.4 Pentane 1.8 Sugar 1.8 Pentanol 14.8 Sulfur trioxide 3.1 Pentene 2 Sulfuric acid 21.9 Perchlorate 3.6 Sulfuric acid (17%) 31 Perlite 1.7 Sulfuric acid (97%) 8.6 PET powder 1.5 Sulphur 3.5 Phenetole 4.2 Sulphur Dioxide 14 Phenol 8 Sunflower seeds 2 Phenol resin 7.4 T Phosgene 4.3 Talcum 1.5 Phosphate 4 Tankage 1.9 Phosphorus salt 4 Tar 4 Phosphorus. liquid 3.9 Tartaric acid 35.9 Pinane 2.1 Tea powder 2 Piperidine 5.8 Terephthalic acid 1.5 Plastic pellets 1.2 Terpinene 2.7 Polyamide pellets 1.7 Terpinolene 2.3 Polyethylene 1.2 Tetrachlorethylene 2.5 Polypropylene 1.6 Thomaskali dust 3.4 Polyrol 2.8 Thujone (0°C) 10.8 Polyvinyl acetals 2.8 Tinder 12 Popcorn 1.1 Titan tetrachloride 2.8 Potash salt 2 Tobacco dust 1.8 Potato starch 1.7 Toluene 2.4 Pril 1.2 Tooth paste 18.3 Printing ink 4.6 Transformer oil 2.1 Propanoic acid 3.2 Trichloroethylene 3.2 Propanol (propyl alcohol) 2.2 Triethylaluminium 2.9 Propionaldehyde 14.4 Triptan 1.9 Propylamine 3 U Propylene chloride 9 Ultrasil 1.4 Propylene. liquid 1.9 Undecan 2 Propylether 3.3 Urea 2.9 PVC powder. pure 1.3 V Pyridine 13.2 Valeric acid 2.7 Pyrroles 8 Vinegar 24 Q Viscose 34.5 Quartz stone meal 2.7 W Quinoline 8.8 Water 80.3 R Water (360°C) 10 Rapeseed 3.3 Water. demineralisiert 29.3 Rapeseed grist 2.1 Water. heavy 78.3 Resin 1.5 Water-in-oil-emulsion 24.2 Rice 3 Wax 1.8 Rock salt (0-25 mm) 4.3 Wheat 4 Rapeseed grist 2.1 Wheat starch 2.5 Resin 1.5 White spirit 2 Rice 3 Wine 25 Rock salt (0-25 mm) 4.3 Wood chips 2.3 Rye 6 Wood swarf 1.5 Rye bran 2.2 X S Xylene 2.3 Saccharose solution 20 Xylitol 40 Salt water 32 Z Sawdust 1.3 Zinc oxide 1.5 Silica sand 2 Zinc powder 4.4 Silicic acid 2.
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]
  • Preparation of a Germole-Containing Π-Conjugated Polymer by the Te–Li
    Zheng et al. NPG Asia Materials (2020) 12:41 https://doi.org/10.1038/s41427-020-0224-9 NPG Asia Materials ARTICLE Open Access Preparation of a germole-containing π-conjugated polymer by the Te–Li exchange reaction of a tellurophene-containing polymer Feng Zheng1,Sia-ErTan1, Yuki Yanamoto1, Naoki Shida 1, Hiroki Nishiyama1, Shinsuke Inagi1 and Ikuyoshi Tomita 1 Abstract The synthesis and optoelectronic functions of a germole-containing π-conjugated polymer prepared by the reaction of a lithiated polymer precursor are described. A regioregular organometallic polymer having 1,4-dilithio-1,3-butadiene and 9,9-dioctylfluorene-2,7-diyl units was generated by the reaction of a tellurophene-containing polymer having a number-average molecular weight (Mn) and molecular weight distribution (Mw/Mn) of 5900 and 1.9, respectively, with n-butyllithium (2.4 equiv) at −78 to −60 °C for 3 h. The prepared lithiated polymer was reacted with dimethylgermanium dichloride (1.5 equiv) at −60 °C to ambient temperature for 12 h in tetrahydrofuran to produce a π-conjugated polymer possessing 1,1-dimethylgermole-2,5-diyl units in 76% yield (Mn = 4400 and Mw/Mn = 1.7). The absorption maximum and onset of the obtained polymer were observed at 465 and 535 nm, respectively, in the UV-vis spectrum, from which the optical band gap of the polymer was estimated to be 2.31 eV. In the photoluminescence spectrum, the obtained polymer exhibits green fluorescence with an emission maximum of 547 nm and a quantum yield of 0.04. The chemical interaction of the dimethylgermole-containing π-conjugated polymer with fluoride was also examined in terms of the changes observed in the UV-vis absorption spectra.
    [Show full text]
  • Process for Producing Fused-Ring Aromatic Compound, and Conjugated Polymer
    (19) TZZ ¥__T (11) EP 2 774 931 A1 (12) EUROPEAN PATENT APPLICATION published in accordance with Art. 153(4) EPC (43) Date of publication: (51) Int Cl.: 10.09.2014 Bulletin 2014/37 C07F 19/00 (2006.01) C07F 7/08 (2006.01) C07F 7/22 (2006.01) C07F 7/30 (2006.01) (2006.01) (2014.01) (21) Application number: 12844675.4 C08G 61/12 H01L 31/04 (22) Date of filing: 02.11.2012 (86) International application number: PCT/JP2012/078517 (87) International publication number: WO 2013/065836 (10.05.2013 Gazette 2013/19) (84) Designated Contracting States: • KAWAI, Jyunya AL AT BE BG CH CY CZ DE DK EE ES FI FR GB Yokohama-shi GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO Kanagawa 227-8502 (JP) PL PT RO RS SE SI SK SM TR •SATO,Wataru Yokohama-shi (30) Priority: 02.11.2011 JP 2011241498 Kanagawa 227-8502 (JP) 29.11.2011 JP 2011260973 • SATAKE, Kenichi Yokohama-shi (71) Applicant: Mitsubishi Chemical Corporation Kanagawa 227-8502 (JP) Chiyoda-ku • FURUYA, Mitsunori Tokyo 100-8251 (JP) Yokohama-shi Kanagawa 227-8502 (JP) (72) Inventors: • FUJITA, Rieko (74) Representative: HOFFMANN EITLE Yokohama-shi Patent- und Rechtsanwälte Kanagawa 227-8502 (JP) Arabellastrasse 4 81925 München (DE) (54) PROCESS FOR PRODUCING FUSED-RING AROMATIC COMPOUND, AND CONJUGATED POLYMER (57) The invention addresses a problem of purifying having n active groups (wherein n is an integer of 1 or a monomer to be a precursor according to a simpler and more and 4 or less), which comprises bringing a compo- milder method so as to obtain a polymer having a higher sition containing the condensed polycyclic aromatic com- molecular weight.
    [Show full text]
  • WO 2015/025175 Al 26 February 2015 (26.02.2015) 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 2015/025175 Al 26 February 2015 (26.02.2015) P O P C T (51) International Patent Classification: (81) Designated States (unless otherwise indicated, for every C09K 5/06 (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/GB2014/052580 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, 22 August 2014 (22.08.2014) KZ, LA, LC, LK, LR, LS, LT, LU, LY, MA, MD, ME, MG, MK, MN, MW, MX, MY, MZ, NA, NG, NI, NO, NZ, (25) Filing Language: English OM, PA, PE, PG, PH, PL, PT, QA, RO, RS, RU, RW, SA, (26) Publication Language: English SC, SD, SE, SG, SK, SL, SM, ST, SV, SY, TH, TJ, TM, TN, TR, TT, TZ, UA, UG, US, UZ, VC, VN, ZA, ZM, (30) Priority Data: ZW. 13 15098.2 23 August 2013 (23.08.2013) GB (84) Designated States (unless otherwise indicated, for every (71) Applicant: SUNAMP LIMITED [GB/GB]; Unit 1, Satel kind of regional protection available): ARIPO (BW, GH, lite Place, Macmerry, Edinburgh EH33 1RY (GB). GM, KE, LR, LS, MW, MZ, NA, RW, SD, SL, ST, SZ, TZ, UG, ZM, ZW), Eurasian (AM, AZ, BY, KG, KZ, RU, (72) Inventors: BISSELL, Andrew John; C/o SunAmp, Unit TJ, TM), European (AL, AT, BE, BG, CH, CY, CZ, DE, 1, Satellite Place, Macmerry, Edinburgh EH33 1RY (GB).
    [Show full text]
  • Alphabetical Index of Substances and Articles
    ALPHABETICAL INDEX OF SUBSTANCES AND ARTICLES - 355 - 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. - 356 - INDEX Name and description Class UN No. Name and description Class UN No. Accumulators, electric, see 4.3 3292 Acid mixture, nitrating acid, see 8 1796 8 2794 8 2795 Acid mixture, spent, nitrating acid, see 8 1826 8 2800 8 3028 Acraldehyde, inhibited, see 6.1 1092 ACETAL 3 1088
    [Show full text]
  • Synthesis and Characterization of Bis[1]Benzothieno[3,2-B:20,30-D]Pyrroles: Quantitative Effects of Benzannulation on Dithieno[3,2-B:20,30-D]Pyrroles
    molecules Article Synthesis and Characterization of Bis[1]benzothieno[3,2-b:20,30-d]pyrroles: Quantitative Effects of Benzannulation on Dithieno[3,2-b:20,30-d]pyrroles Rylan M. W. Wolfe , Evan W. Culver and Seth C. Rasmussen * Department of Chemistry and Biochemistry, North Dakota State University, NDSU Dept. 2735, P.O. Box 6050, Fargo, ND 58108-6050, USA; [email protected] (R.M.W.W.); [email protected] (E.W.C.) * Correspondence: [email protected]; Tel.: +1-701-231-8747 Received: 14 August 2018; Accepted: 3 September 2018; Published: 6 September 2018 Abstract: The synthesis of four N-functionalized bis[1]benzothieno[3,2-b:20,30-d]pyrroles (BBTPs) is reported in order to provide a more detailed characterization of these fused-ring units, as well as increase the scope of known BBTP units available for application to conjugated materials. The optical, electronic, and structural properties of the resulting BBTP units have been compared to the parent N-alkyl- and N-aryl-dithieno[3,2-b:20,30-d]pyrroles (DTPs), as well as their corresponding 2,6-diphenyl derivatives, in order to fully quantify the relative electronic effects resulting from benzannulation of the parent DTP building block. Such comparative analysis reveals that benzannulation results in a red-shifted absorbance, but to a lesser extent than simple phenyl-capping of the DTP. More surprising is that benzannulation results in stabilization of the BBTP HOMO, compared to the destabilization normally observed with extending the conjugation length of the backbone. Keywords: fused-ring thiophenes; heteroacenes; dithieno[3,2-b:20,30-d]pyrroles; benzannulation; structure-function relationships 1.
    [Show full text]
  • 4050 Safety Wash
    4050 Safety Wash MG Chemicals UK Limited Version No: A-2.00 Issue Date: 26/03/2019 Safety data sheet according to REACH Regulation (EC) No 1907/2006, as amended by UK REACH Regulations SI 2019/758 Revision Date: 22/04/2021 L.REACH.GB.EN SECTION 1 Identification of the substance / mixture and of the company / undertaking 1.1. Product Identifier Product name 4050 Synonyms SDS Code: 4050-Liquid; 4050-1L, 4050-4L, 4050-20L | UFI: 58R0-10PR-8006-PNCW Other means of identification Safety Wash for Electronics 1.2. Relevant identified uses of the substance or mixture and uses advised against Relevant identified uses Cleaner for electronics that is safe for plastics Uses advised against Not Applicable 1.3. Details of the supplier of the safety data sheet Registered company name MG Chemicals UK Limited MG Chemicals (Head office) Heame House, 23 Bilston Street, Sedgely Dudley DY3 1JA United Address 9347 - 193 Street Surrey V4N 4E7 British Columbia Canada Kingdom Telephone +(44) 1663 362888 +(1) 800-201-8822 Fax Not Available +(1) 800-708-9888 Website Not Available www.mgchemicals.com Email [email protected] [email protected] 1.4. Emergency telephone number Association / Organisation Verisk 3E (Access code: 335388) Emergency telephone +(44) 20 35147487 numbers Other emergency telephone +(0) 800 680 0425 numbers SECTION 2 Hazards identification 2.1. Classification of the substance or mixture Classification according to regulation (EC) No 1272/2008 H225 - Flammable Liquid Category 2, H319 - Eye Irritation Category 2 [CLP] and amendments [1] Legend: 1. Classified by Chemwatch; 2. Classification drawn from Regulation (EU) No 1272/2008 - Annex VI 2.2.
    [Show full text]
  • Chemical Formula of Binary Ionic Compounds – Sheet 1 the Combining Power Or Valency of Silver Is Always 1
    Chemical Formula of Binary Ionic Compounds – Sheet 1 The combining power or valency of silver is always 1. All other transition metals are 2 unless otherwise indicated. No. Binary compound Formula No. Binary compound Formula 1 potassium fluoride 26 calcium sulfide 2 calcium chloride 27 lithium bromide 3 barium bromide 28 nickel sulfide 4 silver sulfide 29 zinc phosphide 5 aluminium iodide 30 barium iodide 6 potassium iodide 31 caesium chloride 7 lead(IV) oxide 32 copper bromide 8 zinc nitride 33 sodium nitride 9 silver iodide 34 silver chloride 10 barium fluoride 35 sodium hydride 11 lead(II) iodide 36 potassium nitride 12 silver fluoride 37 cobalt chloride 13 sodium sulfide 38 magnesium sulfide 14 sodium bromide 39 potassium chloride 15 calcium oxide 40 calcium bromide 16 zinc fluoride 41 iron(III) oxide 17 strontium phosphide 42 aluminium fluoride 18 barium sulfide 43 magnesium bromide 19 aluminium oxide 44 iron(III) chloride 20 aluminium chloride 45 barium nitride 21 aluminium sulfide 46 sodium fluoride 22 lead(II) oxide 47 lithium fluoride 23 barium chloride 48 lithium iodide 24 copper chloride 49 lithium hydride 25 barium phosphide 50 potassium oxide “Aluminum” and “cesium” are commonly used alternative spellings for "aluminium" and "caesium that are used in the US. May be freely copied for educational use. ©www.chemicalformula.org Chemical Formula of Binary Ionic Compounds – Sheet 2 The combining power or valency of silver is always 1. All other transition metals are 2 unless otherwise indicated. No. Binary compound Formula No.
    [Show full text]
  • Safety Data Sheet
    SAFETY DATA SHEET 1. Identification Product identifier Aluminum Bromide (AlBr3) Other means of identification SDS number 1AN Materion Code 1AN CAS number 7727-15-3 Synonyms ALUMINUM BROMIDE * ALUMINUM TRIBROMIDE Manufacturer/Importer/Supplier/Distributor information Manufacturer Company name Materion Advanced Chemicals Inc. Address 407 N 13th Street 1316 W. St. Paul Avenue Milwaukee, WI 53233 United States Telephone 414.212.0257 E-mail [email protected] Contact person Noreen Atkinson Emergency phone number Chemtrec 800.424.9300 2. Hazard(s) identification Physical hazards Corrosive to metals Category 1 Health hazards Acute toxicity, oral Category 3 Skin corrosion/irritation Category 1 Serious eye damage/eye irritation Category 1 Environmental hazards Not classified. OSHA defined hazards Not classified. Label elements Signal word Danger Hazard statement Toxic if swallowed. May be corrosive to metals. Causes severe skin burns and eye damage. Causes serious eye damage. Precautionary statement Prevention Keep only in original container. Wash thoroughly after handling. Do not eat, drink or smoke when using this product. Wear protective gloves/protective clothing/eye protection/face protection. Response If swallowed: Rinse mouth. Do NOT induce vomiting. If on skin (or hair): Take off immediately all contaminated clothing. Rinse skin with water/shower. If inhaled: Remove person to fresh air and keep comfortable for breathing. If in eyes: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing. Immediately call a POISON CENTER or doctor/physician. Specific treatment (see this label). Absorb spillage to prevent material damage. Storage Store locked up. Store in corrosive resistant container with a resistant inner liner.
    [Show full text]
  • United States Patent (19) 11 Patent Number: 5,936,127 Zhang (45) Date of Patent: Aug
    USOO5936127A United States Patent (19) 11 Patent Number: 5,936,127 Zhang (45) Date of Patent: Aug. 10, 1999 54 ASYMMETRIC SYNTHESIS AND CATALYSIS Jacobsen, E.N., “Asymmetric Catalytic Epoxidation of WITH CHIRAL, HETEROCYCLIC Unfunctionalized Olefins,” Catalytic Asymmetric Synthesis, COMPOUNDS Chapter 4.2, 159-202 (1993). Smith, M.B., “Retrosynthesis, Stereochemistry and Confor 75 Inventor: Xumu Zhang, State College, Pa. mations,” Organic Synthesis, Chapter 1.4.C., 58-63 (1994). Trost, B.M. & Li, C.-J., “Novel Umpolung in C-C Bond 73 Assignee: The Penn State Research Foundation, Formation Catalyzed by Triphenylphosphine,” J. AM. University Park, Pa. Chem. Soc., 116, 31.67-3168 (1994). Zhang, C. & Lu, X., “Phosphine-Catalyzed Cycloaddition 21 Appl. No.: 09/006,178 of 2,3-Butadienoates or 2-Butynoates with Electron-Defi cient Olefins. A Novel 3+2 Annulation Approach to Cyclo 22 Filed: Jan. 13, 1998 pentenes,” J. Org. Chem. 60,2906–2908 (1995). Aggarwal, V.K. et al., “A Novel Catalytic Cycle for the Related U.S. Application Data Synthesis of Epoxides Using Sulfure Ylides,” Chem. Eur: 60 Provisional application No. 60/035,187, Jan. 13, 1997, and Journal, 1024–1030 (1996). provisional application No. 60/046,117, May 9, 1997. Aggarwal, V.K., et al., “Direct Asymmetric Epoxidation of Aldehydes Using Catalytic Amounts of Enantiomerically 51 Int. Cl. ........................... C07F 9/02; CO7D 333/50; Pure Sulfides,” J. Am. Chem. Soc., 118, 7004-7005 (1996). CO7D 209/56; B01J 31/00 Basavaiah, D, et al., “The Baylis-Hillman Reaction: A 52 U.S. Cl. ................................. 568/12; 549/41; 549/43; Novel Carbon-Carbon bond Forming Reaction.” Tetrahe 548/418; 548/427: 548/452; 502/162; 502/168 dron, 52,8001-8062 (1996).
    [Show full text]
  • 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
    [Show full text]
  • Year 9 Chemistry Workbook the Polesworth School Chemical
    Year 9 Chemistry Workbook The Polesworth School Chemical Changes 1 Chemical Changes Mastery Booklet This booklet covers: 1. Formulae of ionic compounds 2. Reactivity of metals 3. Extraction of metals 4. Acids 5. Ionic equations 6. Half equations 7. Electrolysis Part 1: Formulae of ionic compounds Recap questions: 1. Draw an atom of beryllium showing all its electrons 2. Draw an atom of oxygen showing all its electrons 3. In words, explain what occurs in terms of electrons when beryllium reacts with oxygen 4. Draw out the two ions formed in this reaction 5. Repeat the process, but for lithium reacting with oxygen 6. Use the above to explain why the formula for lithium oxide is Li2O but the formula for beryllium oxide is BeO 7. Challenge: Predict the formulae of: a. Lithium fluoride c. Aluminium nitride e. Aluminium oxide b. Lithium nitride d. Aluminium chloride f. Magnesium nitride There are many different ways to predict the formulae of ionic compounds. In terms of working out which charge the ion has: • Group 1: 1+ • Group 2: 2+ • Group 3: 3+ • Group 5: 3- • Group 6: 2- • Group 7: 1- • Transition metals have their charge given by a Roman numeral, e.g. copper (II) is Cu2+ • Some ions can be compounds: Name Formula Example + Ammonium ion NH4 Ammonium chloride, NH4Cl - Hydroxide ion OH Calcium hydroxide. Ca(OH)2 2- Sulphate ion SO4 Sodium sulphate, Na2SO4 2- Carbonate ion CO3 Calcium carbonate, CaCO3 - Nitrate ion NO3 Magnesium nitrate, Mg(NO3)2 Note that you use brackets to multiply the compound ion. Practice – 8.
    [Show full text]