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Trimethylacetic Formic Anhydride Precipitation from Ethanol and Diethyl Ether, M.P
PDF hosted at the Radboud Repository of the Radboud University Nijmegen The following full text is a publisher's version. For additional information about this publication click this link. http://hdl.handle.net/2066/16408 Please be advised that this information was generated on 2021-09-24 and may be subject to change. 460 Edward J. Vlietsira et al. / Trimethylacetic formic anhydride precipitation from ethanol and diethyl ether, m.p. 240°C (dec.); Acknowledgements [a]5 5 —140° (c 1.0, water). MS: M* 700. We thank Mr. P. Kranenburg for valuable technical as N-(6,14-endo-Etheno-7,8-dihydromorphine-7ai-carbonyl)-L- sistance and Messrs. J. A. de Groot, L. J. M. Helvensteijn -phenylalanyl-L-leucinol (14) and E. F. Lameijer for carrying out preliminary experi The hydrochloride of 12 (1.63 g, 2.4 mmol) was converted into the ments. We are grateful to the Management of Diosynth base and dissolved in 30 ml of anhydrous 2-propanol. To this B. V., Apeldoorn, The Netherlands, for gifts of chemicals. solution, 1.5 g (15 mmol) of anhydrous calcium chloride and We thank the U.S.A. Committee on Problems of Drug 1.14 g (30 mmol) of sodium tetrahydroborate were added. The Dependence and Dr. A. E. Jacobson, Biological Coordi conversion was complete (TLC) after 6 days at 35°C. Water nator, for the results of the pharmacological studies. We (50 ml) was then added and the mixture acidified with 2 N hydro gen chloride to pH 2-3. Extraction with a mixture of chloroform are indebted to Dr. -
Toxicological Basis Data for the Derivation of EU-LCI Values For
TEXTE 223/2020 Toxicological basis data for the derivation of EU- LCI values for neopentyl glycol, diisobutyl succinate, diisobutyl glutarate, 1,2- dimethoxyethane and 1,2-diethoxyethane Final report German Environment Agency TEXTE 223/2020 Ressortforschungsplan of the Federal Ministry for the Enviroment, Nature Conservation and Nuclear Safety Project No. (FKZ) 3719 62 205 0 Report No. FB000359/ENG Toxicological basis data for the derivation of EU-LCI values for neopentyl glycol, diisobutyl succinate, diisobutyl glutarate, 1,2- dimethoxyethane and 1,2-diethoxyethane Final report by Dr. Barbara Werschkun Wissenschaftsbüro, Berlin On behalf of the German Environment Agency Imprint Publisher Umweltbundesamt Wörlitzer Platz 1 06844 Dessau-Roßlau Tel: +49 340-2103-0 Fax: +49 340-2103-2285 [email protected] Internet: www.umweltbundesamt.de /umweltbundesamt.de /umweltbundesamt Report performed by: Wissenschaftsbüro Dr. Barbara Werschkun Monumentenstr. 31a 10829 Berlin Germany Report completed in: May 2020 Edited by: Section II 1.3 Indoor Hygiene, Health-related Environmental Impacts Dr. Ana Maria Scutaru Publication as pdf: http://www.umweltbundesamt.de/publikationen ISSN 1862-4804 Dessau-Roßlau, December 2020 The responsibility for the content of this publication lies with the author(s). TEXTE Toxicological basis data for the derivation of EU-LCI values for neopentyl glycol, diisobutyl succinate, diisobutyl glutarate, 1,2-dimethoxyethane and 1,2-diethoxyethane – Final report Abstract: Toxicological basis data for the derivation of EU-LCI values for neopentyl glycol, diisobutyl succinate, diisobutyl glutarate, 1,2-dimethoxyethane and 1,2-diethoxyethane The objective of this study was the evaluation of toxicological data for five substances as basis for the derivation of EU-LCI values. -
Octyl Alcohol F Oxo Alcohols
Octyl alcohol F Oxo alcohols Trade name: Octyl alcohol F Chemical name: Distillation residue, by-products from the production of 2-ethylhexan-1-ol. CN: 3824 90 97 CAS: 68609-68-7 Properties Use Octyl alcohol F is a liquid whose colour varies from yellow, Octyl alcohol F is used as a flotation agent. through brown-yellow to greenish, with a characteristic odour. Product classification Octyl alcohol F is not classified as a hazardous material according to RID/ADR. Physical and chemical properties Parameter Business unit Value Test methods 2-ethylhexanol, not more than % m/m 30 ZAK’s internal rmethod High-molecular compounds >C8, not less than % m/m 70 ZAK’s internal rmethod oxoplast.pl Manufacturer: Grupa Azoty Zakłady Azotowe Kędzierzyn S.A. Isobutyraldehyde Trade name: Isobutyraldehyde Chemical name: 2-methylpropanal, isobutyraldehyde, isobutanal CN: 2912 19 00 CAS: 78-84-2 Chemical formula: (CH3)2CHCHO Properties Use Isobutyraldehyde is a transparent, colourless liquid with a char- Isobutyraldehyde is used as a raw material for producing acteristic odour. alcohols, acids, amines, and esters. It is used in processes of manufacturing plasticizers, pharmaceutical products, plant Product classification protection agents, synthetic resins, fragrances, solvents and all sorts of additives used in many branches of industry Isobutyraldehyde is classified as a hazardous material (antioxidants, wetting agents, perfume ingredients, improvers). according to RID/ADR. - RID KI. 3, packing group II - ADR KI. 3, packing group II Physical and chemical properties Parameter Business unit Value Test methods Colour, not more than Pt-Co 15 ISO 6271 Acid number, not more than mg KOH/g 2 ZAK’s internal rmethod N-butyraldehyde, not more than % m/m 0,2* ZAK’s internal rmethod Water, not more than % m/m 1,5 ISO 760 Isobutyraldehyde, not less than % m/m 99,5* ZAK’s internal rmethod * the values do not take into account water content in the product oxoplast.pl Manufacturer: Grupa Azoty Zakłady Azotowe Kędzierzyn S.A. -
SODIUM FORMATE, Hydrate
CXSO045 - SODIUM FORMATE, hydrate SODIUM FORMATE, hydrate Safety Data Sheet CXSO045 Date of issue: 04/04/2017 Version: 1.0 SECTION 1: Identification 1.1. Product identifier Product name : SODIUM FORMATE, hydrate Product code : CXSO045 Product form : Substance Physical state : Solid Formula : CHNaO2 Synonyms : FORMIC ACID, ZINC SALT, DIHYDRATE DIFORMATOZINC DIHYDRATE ZINC DIFORMATE DIHYDRATE Chemical family : METAL COMPOUND 1.2. Recommended use of the chemical and restrictions on use Recommended use : Chemical intermediate For research and industrial use only 1.3. Details of the supplier of the safety data sheet GELEST, INC. 11 East Steel Road Morrisville, PA 19067 USA T 215-547-1015 - F 215-547-2484 - (M-F): 8:00 AM - 5:30 PM EST [email protected] - www.gelest.com 1.4. Emergency telephone number Emergency number : CHEMTREC: 1-800-424-9300 (USA); +1 703-527-3887 (International) SECTION 2: Hazard(s) identification 2.1. Classification of the substance or mixture GHS-US classification Not classified 2.2. Label elements GHS-US labeling No labeling applicable 2.3. Hazards not otherwise classified (HNOC) No additional information available 2.4. Unknown acute toxicity (GHS US) No data available SECTION 3: Composition/Information on ingredients 3.1. Substances Substance type : Mono-constituent Name : SODIUM FORMATE, hydrate CAS No : 141-53-7 Name Product identifier % GHS-US classification Sodium formate (CAS No) 141-53-7 95 - 100 Not classified Full text of hazard classes and H-statements : see section 16 3.2. Mixtures Not applicable 4.1. Description of first aid measures First-aid measures general : Remove contaminated clothing and shoes. -
EPA Method 8315A (SW-846): Determination of Carbonyl Compounds by High Performance Liquid Chromatography (HPLC)
METHOD 8315A DETERMINATION OF CARBONYL COMPOUNDS BY HIGH PERFORMANCE LIQUID CHROMATOGRAPHY (HPLC) 1.0 SCOPE AND APPLICATION 1.1 This method provides procedures for the determination of free carbonyl compounds in various matrices by derivatization with 2,4-dinitrophenylhydrazine (DNPH). The method utilizes high performance liquid chromatography (HPLC) with ultraviolet/visible (UV/vis) detection to identify and quantitate the target analytes. This method includes two procedures encompassing all aspects of the analysis (extraction to determination of concentration). Procedure 1 is appropriate for the analysis of aqueous, soil and waste samples and stack samples collected by Method 0011. Procedure 2 is appropriate for the analysis of indoor air samples collected by Method 0100. The list of target analytes differs by procedure. The appropriate procedure for each target analyte is listed in the table below. Compound CAS No. a Proc. 1b Proc. 2 b Acetaldehyde 75-07-0 X X Acetone 67-64-1 X Acrolein 107-02-8 X Benzaldehyde 100-52-7 X Butanal (Butyraldehyde) 123-72-8 X X Crotonaldehyde 123-73-9 X X Cyclohexanone 108-94-1 X Decanal 112-31-2 X 2,5-Dimethylbenzaldehyde 5779-94-2 X Formaldehyde 50-00-0 X X Heptanal 111-71-7 X Hexanal (Hexaldehyde) 66-25-1 X X Isovaleraldehyde 590-86-3 X Nonanal 124-19-6 X Octanal 124-13-0 X Pentanal (Valeraldehyde) 110-62-3 X X Propanal (Propionaldehyde) 123-38-6 X X m-Tolualdehyde 620-23-5 X X o-Tolualdehyde 529-20-4 X p-Tolualdehyde 104-87-0 X a Chemical Abstract Service Registry Number. -
Toxicological Profile for Formaldehyde
TOXICOLOGICAL PROFILE FOR FORMALDEHYDE U.S. DEPARTMENT OF HEALTH AND HUMAN SERVICES Public Health Service Agency for Toxic Substances and Disease Registry July 1999 FORMALDEHYDE ii DISCLAIMER The use of company or product name(s) is for identification only and does not imply endorsement by the Agency for Toxic Substances and Disease Registry. FORMALDEHYDE iii UPDATE STATEMENT Toxicological profiles are revised and republished as necessary, but no less than once every three years. For information regarding the update status of previously released profiles, contact ATSDR at: Agency for Toxic Substances and Disease Registry Division of Toxicology/Toxicology Information Branch 1600 Clifton Road NE, E-29 Atlanta, Georgia 30333 FORMALDEHYDE vii QUICK REFERENCE FOR HEALTH CARE PROVIDERS Toxicological Profiles are a unique compilation of toxicological information on a given hazardous substance. Each profile reflects a comprehensive and extensive evaluation, summary, and interpretation of available toxicologic and epidemiologic information on a substance. Health care providers treating patients potentially exposed to hazardous substances will find the following information helpful for fast answers to often-asked questions. Primary Chapters/Sections of Interest Chapter 1: Public Health Statement: The Public Health Statement can be a useful tool for educating patients about possible exposure to a hazardous substance. It explains a substance’s relevant toxicologic properties in a nontechnical, question-and-answer format, and it includes a review of the general health effects observed following exposure. Chapter 2: Health Effects: Specific health effects of a given hazardous compound are reported by route of exposure, by type of health effect (death, systemic, immunologic, reproductive), and by length of exposure (acute, intermediate, and chronic). -
Review Article Di-2-Ethylhexylphthalate May Be a Natural Product, Rather Than a Pollutant
Hindawi Journal of Chemistry Volume 2018, Article ID 6040814, 7 pages https://doi.org/10.1155/2018/6040814 Review Article Di-2-ethylhexylphthalate May Be a Natural Product, Rather than a Pollutant Aurelio Ortiz and Estibaliz Sansinenea Facultad de Ciencias Qu´ımicas, Beneme´rita Universidad Auto´noma de Puebla, C.P. 72570, Puebla, PUE, Mexico Correspondence should be addressed to Estibaliz Sansinenea; [email protected] Received 28 June 2018; Revised 22 August 2018; Accepted 3 September 2018; Published 26 September 2018 Academic Editor: Qizhen Du Copyright © 2018 Aurelio Ortiz and Estibaliz Sansinenea. )is is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Di-2-ethylhexylphtalate is an ester of phthalic acid that has been used as plasticizer in many materials. Due to the extended use, it has been persistently found in different environments being classified as a pollutant with some risks for human health. However, in the last years, it has been found that this compound is produced by plants or microorganisms like bacteria or fungi. )is finding opened a serious debate about the origin of this compound and questioned if it is a real pollutant or a natural metabolite with some biological activities that could help us in several ways. )is review tries to give some data of the different points of view about this question. 1. Introduction presence of these compounds in the environment, many reactions have been reported to degrade and transform these Phthalate compounds are colorless liquid chemicals that compounds. -
UNITED STATES PATENT OFFICE 2,629,746 PROCESS of PRODUCING PENTAERYTHRTOL Richard F
Patented Feb. 24, 1953 r - 2,629,746 UNITED STATES PATENT OFFICE 2,629,746 PROCESS OF PRODUCING PENTAERYTHRTOL Richard F. B. Cox, Wilmington, Del, assignor to Hercules Powder Company, Wilmington, Del, a corporation of Delaware No Drawing. Application June 12, 1948, Serial No. 32,737 i Caim. (C. 260-635) 2 ihis application is a continuation-in-part of The process to which this invention relates my copending application Serial Number 459,709, may broadly be described as involving condensa filed September 25, 1942, and now abandoned. tion of acetaldehyde with formaldehyde in an This invention relates to an improved process aqueous medium in the presence of an alkaline for the preparation of pentaerythritol. More catalyst to form a reaction mixture comprising particularly, it is concerned with an improved pentaerythritol and the formate of the catalyst process for recovering pentaerythritol from a cation, Converting said reaction mixture to an Crude reaction mixture obtained by the alkaline aqueous Solution comprising pentaerythritol and Condensation of acetaldehyde and formaldehyde. free formic acid by addition of a substance yield Pentaerythritol is prepared commercially by O ing hydrogen ions in an amount at least chemi condensation of acetaldehyde with formaldehyde cally equivalent to the formate present, extract in an aqueous medium in the presence of an ing formic acid from Said solution with a formic alkaline catalyst such as Ca (CH)2, NaOH, etc. acid solvent substantially water-immiscible and in the resulting reaction mixture there is pres nonsolvent for the pentaerythritol, applying heat ent in addition to the pentaerythritol a metal 15 to evaporate said extracted solution at least to Salt of formic acid, the particular salt depend a point at which Crystallization takes place, and ing upon the catalyst enployed. -
Final Scope of the Risk Evaluation for Formaldehyde CASRN 50-00-0
EPA Document# EPA-740-R-20-014 August 2020 United States Office of Chemical Safety and Environmental Protection Agency Pollution Prevention Final Scope of the Risk Evaluation for Formaldehyde CASRN 50-00-0 August 2020 TABLE OF CONTENTS ACKNOWLEDGEMENTS ......................................................................................................................6 ABBREVIATIONS AND ACRONYMS ..................................................................................................7 EXECUTIVE SUMMARY .....................................................................................................................11 1 INTRODUCTION ............................................................................................................................14 2 SCOPE OF THE EVALUATION ...................................................................................................14 2.1 Reasonably Available Information ..............................................................................................14 Search of Gray Literature ...................................................................................................... 15 Search of Literature from Publicly Available Databases (Peer-reviewed Literature) ........... 16 Search of TSCA Submissions ................................................................................................ 24 2.2 Conditions of Use ........................................................................................................................25 Conditions of Use -
Influence of Impurities in a Methanol Solvent on the Epoxidation of Propylene with Hydrogen Peroxide Over Titanium Silicalite‐1
Supplementary Materials Influence of Impurities in a Methanol Solvent on the Epoxidation of Propylene with Hydrogen Peroxide over Titanium Silicalite‐1 Gang Wang, Yue Li, Quanren Zhu, Gang Li, Chao Zhang, and Hongchen Guo* State Key Laboratory of Fine Chemicals and School of Chemical Engineering, Dalian University of Technology, No. 2 Linggong Road, Dalian 116024, PR China; [email protected] (G.W.); [email protected] (Y.L.); [email protected] (Q.Z.); [email protected] (G.L.); [email protected] (C.Z.) * Correspondence: [email protected]; Tel./Fax: +86‐411‐84986120 Received: 23 November 2019; Accepted: 18 December 2019; Published: date Table S1. Influence of fusel alcohol content on the product distribution and turnover numbers in epoxidation of propylene with H2O2a Conten Selectivity, % Impurity TONb t, wt.% 1M2Pc 2M1Pc PGc DGMEc PGMEc AAc PAc ATc noned 0.00 314.5 0.50 0.52 0.17 0.08 0.00 0.23 0.06 0.00 ethanol 1.00 296.8 0.48 0.46 0.17 0.06 0.01 0.22 0.06 0.00 1.50 286.8 0.45 0.45 0.15 0.05 0.02 0.26 0.06 0.01 2.00 282.9 0.38 0.42 0.14 0.04 0.02 0.28 0.07 0.01 2.50 267.9 0.38 0.41 0.14 0.03 0.03 0.29 0.07 0.01 2‐propanol 0.50 296.8 0.45 0.49 0.17 0.06 0.00 0.21 0.07 0.03 0.75 286.8 0.43 0.47 0.15 0.06 0.00 0.22 0.07 0.05 1.00 282.9 0.41 0.47 0.15 0.04 0.00 0.25 0.08 0.07 1.25 267.9 0.37 0.38 0.14 0.03 0.00 0.26 0.09 0.08 1‐propanol 0.50 297.7 0.51 0.55 0.18 0.06 0.00 0.21 0.11 0.00 0.75 289.0 0.45 0.49 0.18 0.05 0.00 0.22 0.11 0.00 1.00 282.5 0.44 0.49 0.17 0.05 0.00 0.24 0.14 0.01 1.25 266.0 0.43 0.48 0.16 0.05 0.00 0.26 0.14 0.01 Note: a Reaction conditions: pre‐adsorbed TS‐1 powder 0.4 g, fresh methanol or simulated methanol solvents containing ethanol, 2‐propanol and 1‐propanol 35.5 mL, H2O2 (50 wt.%) 4.5 mL, NH3∙H2O (0.32 mol/L) 0.2 mL, propylene pressure 0.6 MPa, 50 ℃, 1 h. -
Diglycidyl Ethers
Europaisches Patentamt (19) J European Patent Office Office europeen des brevets (11) EP0 911 326 A1 (12) EUROPEAN PATENT APPLICATION published in accordance with Art. 158(3) EPC (43) Date of publication: (51) Int. CI.6: C07D 303/27, C08G 59/04 28.04.1999 Bulletin 1999/17 (86) International application number: (21) Application number: 98905732.8 PCT/JP98/00861 (22) Date of filing: 03.03.1998 (87) International publication number: WO 98/3931 4 (1 1 .09.1 998 Gazette 1 998/36) (84) Designated Contracting States: • MURAYAMA, Toshikazu AT BE CH DE DK ES Fl FR GB GR IE IT LI LU MC Yokkaichi-shi, Mie 51 2-091 1 (JP) NL PT SE • TSUZAKI, Nobuko Yokkaichi-shi, Mie 51 2-091 1 (JP) (30) Priority: 04.03.1997 J P 48632/97 (74) Representative: (71 ) Applicant: Kyowa Yuka Co., Ltd. Le Guen, Gerard et al Tokyo 1 00-0004 (JP) CABINET LAVOIX 2, place d'Estienne d'Orves (72) Inventors: 75441 Paris Cedex 09 (FR) • MUTO, Kenji Yokkaichi-shi, Mie551 2-091 1 (JP) (54) DIGLYCIDYL ETHERS (57) The present invention relates to a diglycidyl ether represented by the following general formula (I): R' CH?-CH-CH2-0-CH2-CH-CH2-CH-CH2-O— CH2-CH-CH2 \/ v O 0 (I) (wherein, R1 and R2 are the same or different, and represent lower alkyl having 1-6 carbon atoms), a composition including the glycidyl ether and epoxy resin, and epoxy resin cured product obtained by the composition. The glycidyl ether can be used as a reactive diluent for epoxy resins. -
Purification and Properties of the Inducible Coenzyme A-Linked Butyraldehyde Dehydrogenase from Clostridium Acetobutylicum NEIL R
JOURNAL OF BACTERIOLOGY, JUlY 1988, p. 2971-2976 Vol. 170, No. 7 0021-9193/88/072971-06$02.00/0 Copyright © 1988, American Society for Microbiology Purification and Properties of the Inducible Coenzyme A-Linked Butyraldehyde Dehydrogenase from Clostridium acetobutylicum NEIL R. PALOSAARI* AND PALMER ROGERS Department of Microbiology, University of Minnesota, Minneapolis, Minnesota 55455 Received 13 November 1987/Accepted 25 March 1988 The coenzyme A (CoA)-linked butyraldehyde dehydrogenase (BAD) from Clostridium acetobutylicum was characterized and purified to homogeneity. The enzyme was induced over 200-fold, coincident with a shift from an acidogenic to a solventogenic fermentation, during batch culture growth. The increase in enzyme activity was found to require new protein synthesis since induction was blocked by the addition of rifampin and antibody against the purified enzyme showed the appearance of enzyme antigen beginning at the shift of the fermentation and increasing coordinately with the increase in enzyme specific activity. The CoA-linked acetaldehyde dehydrogenase was copurified with BAD during an 89-fold purification, indicating that one enzyme accounts for the synthesis of the two aldehyde intermediates for both butanol and ethanol production. Butanol dehydrogenase activity was clearly separate from the BAD enzyme activity on TEAE cellulose. A molecular weight of 115,000 was determined for the native enzyme, and the enzyme subunit had a molecular weight of 56,000 indicating that the active form is a homodimer. Kinetic constants were determined in both the forward and reverse directions. In the reverse direction both the V,ax and the apparent affinity for butyraldehyde and caproaldehyde were significantly greater than they were for acetaldehyde, while in the forward direction, the Vmax for butyryl-CoA was fivefold that for acetyl-CoA.