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United States Patent (19) 11 Patent Number: 6,159,466 Yang Et Al
USOO6159466A United States Patent (19) 11 Patent Number: 6,159,466 Yang et al. (45) Date of Patent: *Dec. 12, 2000 54 AQUEOUS COMPOSITION COMPRISING 4,348,483 9/1982 Skogerson ............................... 435/235 SACCHAROMYCES BOULARDII SEQUELA 4,923,855 5/1990 Jensen et al. ........................... 514/188 AND CHROMIUM GLYCINATE 5,614,553 3/1997 Ashmead et al. ....................... 514/505 DNICOTINATE OTHER PUBLICATIONS 75 Inventors: Ping Yang, Fullerton; Houn Simon Hsia, Foothill Ranch, both of Calif. Vinson et al., Nutrition Reports International, Oct. 1984, vol. 73 Assignee: Viva America Marketing, Inc., Costa 30, No. 4, pp. 911–918. Mesa, Calif. Saner et al., The American Journal of Clinical Nutrition. Oct. 1983, vol. 38, pp. 574–578. * Notice: This patent issued on a continued pros ecution application filed under 37 CFR Uusitupa et al., British Journal of Nutrition, Jul. 1992, vol. 1.53(d), and is subject to the twenty year 68, No. 1, pp. 209–216. patent term provisions of 35 U.S.C. 154(a)(2). Barnett et al. In: "Yeasts. Characterization and Identifica tion'. Cambridge University Press. Second Edition. 1990, 21 Appl. No.: 09/015,758 pp. 595-597. 22 Filed: Jan. 29, 1998 Primary Examiner Sandra E. Saucier Related U.S. Application Data ASSistant Examiner Vera Afremova Attorney, Agent, or Firm-Lyon & Lyon LLP 62 Division of application No. 08/719,572, Sep. 25, 1996. 57 ABSTRACT 51 Int. Cl." ............................. A01N 63/04; C12N 1/18; C12N 1/20; A23L 1/28 The present invention includes a novel yeast Strain of the 52 U.S. Cl. ..................................... 424/93.51; 435/255.2; genus Saccharomyces boulardii sequela PY31 ATCC 74366 435/900; 426/62 that is able to process certain metallic compounds into 58 Field of Search .......................... -
A Guide to Export Controls
Foreign Affairs, Trade and Affaires étrangères, Commerce et Development Canada Développment Canada A Guide To CANADA’S EXPORT CONTROLS December 2012 Introduction The issuance of export permits is administered by the Export Controls Division (TIE) of Foreign Affairs, Trade and Development Canada (DFATD). TIE provides assistance to exporters in determining if export permits are required. It also publishes brochures and Notices to Exporters that are freely available on request and on our website www.exportcontrols.gc.ca. How to contact us: Export Controls Division (TIE) Foreign Affairs, Trade and Development Canada 111 Sussex Drive Ottawa, Ontario K1A 0G2 Telephone: (613) 996-2387 Facsimile: (613) 996-9933 Email: [email protected] For information on how to apply for an export permit and additional information on export controls please refer to our website. To enquire on the status of an export permit application: Recognized EXCOL users can check the status of an export permit application on-line. Non-recognized users can call (613) 996-2387 or email [email protected] and quote your export permit application identification (ref ID) number. Export Controls Division website: www.exportcontrols.gc.ca This Guide, at time of publication, encompasses the list of items enumerated on the Export Control List (ECL) that are controlled for export in accordance with Canadian foreign policy, including Canada’s participation in multilateral export control regimes and bilateral agreements. Unless otherwise specified, the export controls contained in this Guide apply to all destinations except the United States. Canada’s Export Control List can be found at the Department of Justice website at http://canada.justice.gc.ca/. -
Inventory Size (Ml Or G) 103220 Dimethyl Sulfate 77-78-1 500 Ml
Inventory Bottle Size Number Name CAS# (mL or g) Room # Location 103220 Dimethyl sulfate 77-78-1 500 ml 3222 A-1 Benzonitrile 100-47-0 100ml 3222 A-1 Tin(IV)chloride 1.0 M in DCM 7676-78-8 100ml 3222 A-1 103713 Acetic Anhydride 108-24-7 500ml 3222 A2 103714 Sulfuric acid, fuming 9014-95-7 500g 3222 A2 103723 Phosphorus tribromide 7789-60-8 100g 3222 A2 103724 Trifluoroacetic acid 76-05-1 100g 3222 A2 101342 Succinyl chloride 543-20-4 3222 A2 100069 Chloroacetyl chloride 79-04-9 100ml 3222 A2 10002 Chloroacetyl chloride 79-04-9 100ml 3222 A2 101134 Acetyl chloride 75-36-5 500g 3222 A2 103721 Ethyl chlorooxoacetate 4755-77-5 100g 3222 A2 100423 Titanium(IV) chloride solution 7550-45-0 100ml 3222 A2 103877 Acetic Anhydride 108-24-7 1L 3222 A3 103874 Polyphosphoric acid 8017-16-1 1kg 3222 A3 103695 Chlorosulfonic acid 7790-94-5 100g 3222 A3 103694 Chlorosulfonic acid 7790-94-5 100g 3222 A3 103880 Methanesulfonic acid 75-75-2 500ml 3222 A3 103883 Oxalyl chloride 79-37-8 100ml 3222 A3 103889 Thiodiglycolic acid 123-93-3 500g 3222 A3 103888 Tetrafluoroboric acid 50% 16872-11-0 1L 3222 A3 103886 Tetrafluoroboric acid 50% 16872-11-0 1L 3222 A3 102969 sulfuric acid 7664-93-9 500 mL 2428 A7 102970 hydrochloric acid (37%) 7647-01-0 500 mL 2428 A7 102971 hydrochloric acid (37%) 7647-01-0 500 mL 2428 A7 102973 formic acid (88%) 64-18-6 500 mL 2428 A7 102974 hydrofloric acid (49%) 7664-39-3 500 mL 2428 A7 103320 Ammonium Hydroxide conc. -
Study of the Modifications of Manganese Dioxide
U. S. Department of Commerce Research Paper RP1941 National Bureau of Standards Volume 41, December 1948 Part of the Journal of Research of the National Bureau of Standards Study of the Modifications of Mangan,ese Dioxide By Howard F. McMurdie and Esther Golovato P ast work on the modificat ions of manganese dioxide of in terest in dry-cell manufacture is revie wed. New X -ray data, at both room and elevaLcd temperatures, combined 'with differen tial hea ting curves lead to the concl usion that five type of manga nese dioxide exi t : (1) well-crystallized p yrolusite ; (2) gamma m a nganese diox ide, a poorly crystalli zed pyrol u site; (3) ramsdellite ; (4) cryp tomelane, a form co ntaining esse ntial p otassium or sodiulll.; a nd (5) delta m anganese dioxide, belie ved to be a poorly crystallize d cryptomela ne. The high-temperature X-r ay diffraction data indicated the phase cha nges t hat cause the heating curve effects. A new crystal fo rm of manganosic oxide (Mn30 4), stable above 1,1700 C, w ~ s fo und t o be cubic of spinel structure. Fincness dcten n inaLion by both thc nitrogen a dsorp t ion and Lhe X-ray line broadening me thods were made on selected samples. I. Introduction this equipment a fla t specinlen is used, and no During the years 1940- 46 there wa increased special teclmiq Ll es were employed to prcven t pre researeh on dry cells. This was stimulated by fcn 'cd orientation. It is r ealized that in a few increased demand for the cell as well a new u es cascs this may have res ulted in r elative intcnsitics for them , combined with certain hor Lages of raw that differ from those in other r eporLs. -
Durham E-Theses
Durham E-Theses Halogenated diazines and triazines Wood, D. E. How to cite: Wood, D. E. (1978) Halogenated diazines and triazines, Durham theses, Durham University. Available at Durham E-Theses Online: http://etheses.dur.ac.uk/8324/ Use policy The full-text may be used and/or reproduced, and given to third parties in any format or medium, without prior permission or charge, for personal research or study, educational, or not-for-prot purposes provided that: • a full bibliographic reference is made to the original source • a link is made to the metadata record in Durham E-Theses • the full-text is not changed in any way The full-text must not be sold in any format or medium without the formal permission of the copyright holders. Please consult the full Durham E-Theses policy for further details. Academic Support Oce, Durham University, University Oce, Old Elvet, Durham DH1 3HP e-mail: [email protected] Tel: +44 0191 334 6107 http://etheses.dur.ac.uk UNIVERSITY OF Du'RKAM A THESIS entitled HALOGENATED DIAZINES AND TRIAZINES Submitted by D E. WOOD (Grey), B Sc (London) The copyright of this thesis rests with the author No quotation from it should be published without his prior written consent and information derived from it should be acknowledged A candidate for the degree of Doctor of Philosophy 19 78 sr i i > j J To my MoLhcr and FaLhcr WLLII Lh.inks for .ill LhaL Lhey have done ACKNOWLEDGEMLNTS I would like LO express my thanks Lo Professor R D Chambers i under whose guidance this research was undertaken, for considerable encouragement, advice and discussion Thanks are due to Dr R S Matthews for his expert advice with n in r. -
Physical Properties and Data of Optical Materials
Physical Properties and Data of Optical Materials Moriaki Wakaki Keiei Kudo Takehisa Shibuya Laß) CRC Press ^^ J Taylor &. Francis Group '*-*"' Boca Raton London New York CRC Press is an imprint of the Taylor & Francis Group, an informa business • Table of Contents A AI (Aluminum) 1 AlSb (Aluminium Antimonide) 10 ADP (Ammonium Dihydrogen Phosphate) 16 Sb (Antimony) 21 Arsenic Selenium Glass 26 As (33%) + S (30%) + Br (37%) (Arsenic-Sulfur-Bromine Glass) 28 As2Se3 (Arsenic Tri-Selenide) 30 As2S3 (Arsenic Tri-Sulfide Glass) 33 6 Ba (Barium) 39 BaF2 (Barium Fluoride) 42 BaTi03 (Barium Titanate) 47 Be (Beryllium) 50 BeO (Beryllium Oxide) 54 Bi(Bismuth) 56 B(Boron) 61 C Cd(Cadmium) 65 CdSe (Cadmium Selenide) 70 CdS (Cadmium Sulfide) 75 CdTe (Cadmium Telluride) 82 CaC03 (Calcite) 89 CaF2 (Calcium Fluoride) 96 CaW04 (Calcium Tungstate) 105 CsBr (Cesium Bromide) 108 Csl (Cesium Iodide) 113 Cr(Chromium) 118 Cu(Copper) 122 CuCl (Cuprous Chloride) 128 D Diamond 135 G Ga (Gallium) 139 GaSb (Gallium Antimonide) 142 GaAs (Gallium Arsenide) 149 GaP (Gallium Phosphide) 158 Ge (Germanium) 165 Ge + Se + Te (Germanium-Selenium-Tellurium Glass) 180 Glass 182 Au (Gold) 191 * I In (Indium) 199 InSb (Indium Antimonide) 202 InAs (Indium Arsenide) 212 InP (Indium Phosphide) 218 Ir (Iridium) 224 Fe(Iron) 228 L LaF3 (Lanthanum Fluoride) 233 PbF2 (Lead Fluoride) 236 PbSe (Lead Selenide) 237 PbS (Lead Sulfide) 243 PbTe (Lead Telluride) 251 LiF (Lithium Fluoride) 257 Lucite 266 M Mg (Magnesium) 269 MgF2 (Magnesium Fluoride) 275 Mg2Ge (Magnesium Germanide) 282 MgO (Magnesium -
Multivalent Metals and Polyatomic Ions 1
Name Date Comprehension Section 4.2 Use with textbook pages 189–193. Multivalent metals and polyatomic ions 1. Define the following terms: (a) ionic compound (b) multivalent metal (c) polyatomic ion 2. Write the formulae and names of the compounds with the following combination of ions. The first row is completed to help guide you. Positive ion Negative ion Formula Compound name (a) Pb2+ O2– PbO lead(II) oxide (b) Sb4+ S2– (c) TlCl (d) tin(II) fluoride (e) Mo2S3 (f) Rh4+ Br– (g) copper(I) telluride (h) NbI5 (i) Pd2+ Cl– 3. Write the chemical formula for each of the following compounds. (a) manganese(II) chloride (f) vanadium(V) oxide (b) chromium(III) sulphide (g) rhenium(VII) arsenide (c) titanium(IV) oxide (h) platinum(IV) nitride (d) uranium(VI) fluoride (i) nickel(II) cyanide (e) nickel(II) sulphide (j) bismuth(V) phosphide 68 MHR • Section 4.2 Names and Formulas of Compounds © 2008 McGraw-Hill Ryerson Limited 0056_080_BCSci10_U2CH04_098461.in6856_080_BCSci10_U2CH04_098461.in68 6688 PDF Pass 77/11/08/11/08 55:25:38:25:38 PPMM Name Date Comprehension Section 4.2 4. Write the formulae for the compounds formed from the following ions. Then name the compounds. Ions Formula Compound name + – (a) K NO3 KNO3 potassium nitrate 2+ 2– (b) Ca CO3 + – (c) Li HSO4 2+ 2– (d) Mg SO3 2+ – (e) Sr CH3COO + 2– (f) NH4 Cr2O7 + – (g) Na MnO4 + – (h) Ag ClO3 (i) Cs+ OH– 2+ 2– (j) Ba CrO4 5. Write the chemical formula for each of the following compounds. (a) barium bisulphate (f) calcium phosphate (b) sodium chlorate (g) aluminum sulphate (c) potassium chromate (h) cadmium carbonate (d) calcium cyanide (i) silver nitrite (e) potassium hydroxide (j) ammonium hydrogen carbonate © 2008 McGraw-Hill Ryerson Limited Section 4.2 Names and Formulas of Compounds • MHR 69 0056_080_BCSci10_U2CH04_098461.in6956_080_BCSci10_U2CH04_098461.in69 6699 PDF Pass77/11/08/11/08 55:25:39:25:39 PPMM Name Date Comprehension Section 4.2 Use with textbook pages 186–196. -
United States Patent (19) 11) 4,080,491 Kobayashi Et Al
United States Patent (19) 11) 4,080,491 Kobayashi et al. 45) Mar. 21, 1978 54) PROCESS OF PRODUCING RING-OPENING 56 References Cited POLYMERIZATION PRODUCTS U.S. PATENT DOCUMENTS (75) Inventors: Yukio Kobayashi; Takashi Ueshima; 3,798,175 3/1974 Streck .................................. 526/136 Shoichi Kobayashi, all of Yokohama, 3,856,758 - 12/1974 Ueshima ............................... 526/169 Japan 3,859,265 1/1975 Hepworth ............................ 526/281 3,959,234 5/1976 Kurosawa ............................ 526/281 Assignee: Showa Denko K.K., Tokyo, Japan (73) Primary Examiner-Paul R. Michl 21 Appl. No.: 714,833 Attorney, Agent, or Firm-Fitzpatrick, Cella, Harper & 22) Filed: Aug. 16, 1976 Scinto Foreign Application Priority Data 57 ABSTRACT (30) A process of producing a ring-opening polymerization Aug. 27, 1975 Japan ................................ 50-103060 product of a norbornene derivative containing at least Mar. 26, 1976 Japan .................................. 51-32464 one polar group or aromatic group, a norbornadiene Mar. 26, 1976 Japan .................................. 51-32465 derivative containing at least one of said groups or a Apr. 5, 1976 Japan .................................. 51-37274 cycloolefin using a catalyst system prepared from an Apr. 27, 1976 Japan .................................. 51-47268 organometallic compound and the reaction product of May 25, 1976 Japan .................................. 51-59642 tungsten oxide or molybdenum oxide and a phosphorus 51 Int. C.’................................................ C08F 4/78 pentahalide or phosphorus oxytrihalide or these com (52) U.S. C. ..... o e s p s 8 v 8 526/137; 526/113; pounds and other third components. The catalyst sys 526/127; 526/136; 526/169; 526/281; 526/308 temi possesses a high polymerization activity. (58) Field of Search .................... -
Crown Chemical Resistance Chart
Crown Polymers, Corp. 11111 Kiley Drive Huntley, IL. 60142 USA www.crownpolymers.com 847-659-0300 phone 847-659-0310 facisimile 888-732-1270 toll free Chemical Resistance Chart Crown Polymers Floor and Secondary Containment Systems Products: CrownShield covers the following five (4) formulas: CrownShield 50, Product No. 320 CrownCote, Product No. 401 CrownShield 40-2, Product No. 323 CrownShield 28, Product No. 322 CrownPro AcidShield, Product No. 350 CrownCote AcidShield, Product No. 430 CrownPro SolventShield, Product No. 351 CrownCote SolventShield, Product No. 440 This chart shows chemical resistance of Crown Polymers foundational floor and secondary containment product line that would be exposed to chemical spill or immersion conditions. The chart was designed to provide general product information. For specific applications, contact your local Crown Polymers Floor and Secondary Containment Representative or call direct to the factory. ; Resistant to chemical immersion up to 7 days followed by wash down with water 6 Spillage environments that will be cleaned up within 72 hours after initial exposure. 9 Not Recommended Chemical CrownShield SolventShield AcidShield Chemical CrownShield SolventShield AcidShield 1, 4-Dichloro-2-butene 9 6 6 Aluminum Bromate ; ; ; 1, 4-Dioxane 9 6 6 Aluminum Bromide ; ; ; 1-1-1 Trichloroethane 9 ; ; Aluminum Chloride ; ; ; 2, 4-Pentanedione 6 ; 6 Aluminum Fluoride (25%) ; ; ; 3, 4-Dichloro-1-butene 6 6 6 Aluminum Hydroxide ; ; ; 4-Picoline (0-50%) 9 6 6 Aluminum Iodine ; ; ; Acetic Acid (0-15%) 9 6 6 -
1 Abietic Acid R Abrasive Silica for Polishing DR Acenaphthene M (LC
1 abietic acid R abrasive silica for polishing DR acenaphthene M (LC) acenaphthene quinone R acenaphthylene R acetal (see 1,1-diethoxyethane) acetaldehyde M (FC) acetaldehyde-d (CH3CDO) R acetaldehyde dimethyl acetal CH acetaldoxime R acetamide M (LC) acetamidinium chloride R acetamidoacrylic acid 2- NB acetamidobenzaldehyde p- R acetamidobenzenesulfonyl chloride 4- R acetamidodeoxythioglucopyranose triacetate 2- -2- -1- -β-D- 3,4,6- AB acetamidomethylthiazole 2- -4- PB acetanilide M (LC) acetazolamide R acetdimethylamide see dimethylacetamide, N,N- acethydrazide R acetic acid M (solv) acetic anhydride M (FC) acetmethylamide see methylacetamide, N- acetoacetamide R acetoacetanilide R acetoacetic acid, lithium salt R acetobromoglucose -α-D- NB acetohydroxamic acid R acetoin R acetol (hydroxyacetone) R acetonaphthalide (α)R acetone M (solv) acetone ,A.R. M (solv) acetone-d6 RM acetone cyanohydrin R acetonedicarboxylic acid ,dimethyl ester R acetonedicarboxylic acid -1,3- R acetone dimethyl acetal see dimethoxypropane 2,2- acetonitrile M (solv) acetonitrile-d3 RM acetonylacetone see hexanedione 2,5- acetonylbenzylhydroxycoumarin (3-(α- -4- R acetophenone M (LC) acetophenone oxime R acetophenone trimethylsilyl enol ether see phenyltrimethylsilyl... acetoxyacetone (oxopropyl acetate 2-) R acetoxybenzoic acid 4- DS acetoxynaphthoic acid 6- -2- R 2 acetylacetaldehyde dimethylacetal R acetylacetone (pentanedione -2,4-) M (C) acetylbenzonitrile p- R acetylbiphenyl 4- see phenylacetophenone, p- acetyl bromide M (FC) acetylbromothiophene 2- -5- -
Download Author Version (PDF)
Journal of Materials Chemistry A Accepted Manuscript This is an Accepted Manuscript, which has been through the Royal Society of Chemistry peer review process and has been accepted for publication. Accepted Manuscripts are published online shortly after acceptance, before technical editing, formatting and proof reading. Using this free service, authors can make their results available to the community, in citable form, before we publish the edited article. We will replace this Accepted Manuscript with the edited and formatted Advance Article as soon as it is available. You can find more information about Accepted Manuscripts in the Information for Authors. Please note that technical editing may introduce minor changes to the text and/or graphics, which may alter content. The journal’s standard Terms & Conditions and the Ethical guidelines still apply. In no event shall the Royal Society of Chemistry be held responsible for any errors or omissions in this Accepted Manuscript or any consequences arising from the use of any information it contains. www.rsc.org/materialsA Page 1 of 9 Journal of Materials Chemistry A ARTICLE JMCA Safer Salts for CdTe Nanocrystal Solution Processed Solar Cells: The Dual Roles of Ligand Exchange and Grain Growth Received 00th January 20xx, a b c d e Accepted 00th January 20xx Troy K. Townsend, † William B. Heuer, Edward E. Foos, Eric Kowalski, Woojun Yoon and Joseph G. Tischler e DOI: 10.1039/x0xx00000x Inorganic CdSe/CdTe nanocrystals for solid-state photovoltaic devices are typically sintered into a bulk-like material after www.rsc.org/ annealing in the presence of solid cadmium chloride. -
Safety Data Sheet Material Name: HFCL4 SDS ID: 00227583P
Safety Data Sheet Material Name: HFCL4 SDS ID: 00227583P Section 1 - PRODUCT AND COMPANY IDENTIFICATION Material Name HFCL4 Synonyms HAFNIUM TETRACHLORIDE; HAFNIUM (IV) CHLORIDE; (T-4) HAFNIUM CHLORIDE (HfCl4); HAFNIUM CHLORIDE; Cl4Hf Chemical Family metal, halides Product Use semiconductor manufacture Restrictions on Use None known Details of the supplier of the safety data sheet Entegris, Inc. 129 Concord Road Building 2 Billerica, MA 01821 USA Telephone Number: +1-952-556-4181 Telephone Number: +1-800-394-4083 (toll free within North America) Emergency Telephone Number: CHEMTREC - U.S. - 1-800-424-9300 CHEMTREC - Intl. - 1-703-527-3887 E-mail: [email protected] Section 2 - HAZARDS IDENTIFICATION Classification in accordance with paragraph (d) of 29 CFR 1910.1200. Combustible Dust Skin Corrosion/Irritation - Category 1B Serious Eye Damage/Eye Irritation - Category 1 Specific target organ toxicity - Single exposure - Category 3 ( respiratory system ) GHS Label Elements Symbol(s) Signal Word Danger Hazard Statement(s) ____________________________________________________________ Page 1 of 9 Issue date: 2021-05-11 Revision 6.0 Print date: 2021-05-12 Safety Data Sheet Material Name: HFCL4 SDS ID: 00227583P May form combustible dust concentrations in air. Causes severe skin burns and eye damage. May cause respiratory irritation. Precautionary Statement(s) Prevention Do not breathe dust. Wear protective gloves/protective clothing/eye protection/face protection. Wash thoroughly after handling. Use only outdoors or in a well-ventilated area. Response Immediately call a POISON CENTER or doctor/physician. IF INHALED: Remove person to fresh air and keep comfortable for breathing. Specific treatment may be needed, see first aid section of Safety Data Sheet.