4,4'-Methylenediphenyl Diisocyanate (MDI)
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Kinetics of the Reaction Between Alcohols and Isocyanates Catolyzed by Ferric Acetylacetonate
.. -. - Kinetics of the Reaction Between Alcohols and Isocyanates Catolyzed by Ferric Acetylacetonate Leroy Schieler OTS PRICE XEROX $- % i JET PROPULSION LABORATORY I CALIFORNIA INSTITUTE OF TECHNOLOGY PASADENA,CALIFORNIA July 1, 1961 NATIONAL AERONAUTICS AND SPACE ADMINISTRATION CONTRACTNo. NASw-6 Technical Report No. 32-129 Kinetics of the Reaction Between Alcohols and Isocyanates Catalyzed by Ferric Acetylacetonate Leroy Schieler Robert F. Landel, Chief Solid Propellant Chemistry Section JET PROPULSION LABORATORY CALIFORNIA lNSTlTUTE OF TECHNOLOGY PASADENA, CALIFORNIA July 1, 1961 Copyright @ 1961 Jet Propulsion laboratory California Institute of Technology JPL TECHNICAL REPORT NO. 32-129 CONTENTS Page 1. Introduction................................................ 1 II. Kinetics of Ferric Acetylacetonate Catalyzed Urethane Formation ........................................ 3 A . Experimental Methods ..................................... 3 B. Kinetic Investigations ...................................... 3 111 . Dependence of Rate of Urethane Formation on Nature of Reactants ........................................ 11 A . Substituted Isocyanates..................................... 11 B. Substituted Alcohols ....................................... 12 C . Metal Chelate Catalysts ..................................... 12 IV. Conclusions ................................................ 13 References..................................................... 14 TABLES 1. Ferric Acetylacetonate Catalyzed Reaction of a-Naphthyl Isocyanate with -
Safety Data Sheet Acc
Page 1/10 Safety Data Sheet acc. to OSHA HCS Printing date 03/24/2019 Version Number 2 Reviewed on 03/24/2019 * 1 Identification · Product identifier · Trade name: Acrylamide · Part number: RCC-203 · CAS Number: 79-06-1 · EC number: 201-173-7 · Index number: 616-003-00-0 · Application of the substance / the mixture Reagents and Standards for Analytical Chemical Laboratory Use · Details of the supplier of the safety data sheet · Manufacturer/Supplier: Agilent Technologies, Inc. 5301 Stevens Creek Blvd. Santa Clara, CA 95051 USA · Information department: Telephone: 800-227-9770 e-mail: [email protected] · Emergency telephone number: CHEMTREC®: 1-800-424-9300 2 Hazard(s) identification · Classification of the substance or mixture GHS06 Skull and crossbones Acute Tox. 3 H301 Toxic if swallowed. GHS08 Health hazard Muta. 1B H340 May cause genetic defects. Carc. 1B H350 May cause cancer. Repr. 2 H361 Suspected of damaging fertility or the unborn child. STOT RE 1 H372 Causes damage to organs through prolonged or repeated exposure. GHS07 Acute Tox. 4 H312 Harmful in contact with skin. Acute Tox. 4 H332 Harmful if inhaled. Skin Irrit. 2 H315 Causes skin irritation. Eye Irrit. 2A H319 Causes serious eye irritation. Skin Sens. 1 H317 May cause an allergic skin reaction. · Label elements · GHS label elements The substance is classified and labeled according to the Globally Harmonized System (GHS). (Contd. on page 2) US 48.1.26 Page 2/10 Safety Data Sheet acc. to OSHA HCS Printing date 03/24/2019 Version Number 2 Reviewed on 03/24/2019 Trade name: Acrylamide (Contd. -
Report on Carcinogens, Fourteenth Edition for Table of Contents, See Home Page
Report on Carcinogens, Fourteenth Edition For Table of Contents, see home page: http://ntp.niehs.nih.gov/go/roc Naphthalene comes from studies of workers in a coke plant, which found that con- centrations of naphthalene metabolites in the urine were significantly CAS No. 91-20-3 correlated with concentrations of naphthalene in personal air sam- ples (Bieniek 1994, 1997). The first step in the metabolism of naph- Reasonably anticipated to be a human carcinogen thalene is formation of naphthalene-1,2-oxide (as two stereo isomers, First listed in the Eleventh Report on Carcinogens (2004) 1R,2S-oxide and 1S,2R-oxide) through the action of cytochrome P450 enzymes in the presence of the coenzyme NADPH. These oxides are metabolized further by three pathways: (1) hydration by epoxide hy- drolases into dihydrodiols, (2) conjugation by glutathione transferases, and (3) spontaneous rearrangement into 1-naphthol and 2-naph- Carcinogenicity thol, which are converted to naphthoquinones (Chichester et al. 1994, Shultz et al. 1999). Naphthalene is excreted in the urine as the un- Naphthalene is reasonably anticipated to be a human carcinogen changed parent compound or as metabolites, including 1-naphthol, based on sufficient evidence from studies in experimental animals. 2-naphthol, naphthoquinones, dihydroxynaphthalenes, and conju- gated forms, including glutathione, cysteine, glucuronic acid, and Cancer Studies in Experimental Animals sulfate conjugates (NTP 2002). Exposure of rats to naphthalene by inhalation caused nasal tumors, The mechanism by which naphthalene causes cancer is unknown. which are rare in this species. Two types of nasal tumor were ob- A strong correlation has been observed between the rates of forma- served: olfactory epithelial neuroblastoma of the nose, which is a tion of the stereoisomer (1R,2S)-naphthalene oxide in various tissues highly malignant and extremely rare tumor of the lining of the nose, and the selective toxicity of naphthalene to these tissues, suggesting and respiratory epithelial adenoma, which also is rare (NTP 2000). -
Safe Work Procedures for Isocyanate-Containing Products
Safe Work Procedures for Isocyanate-Containing Products June 2000 IATSE Local 891 1640 Boundary Road Vancouver, BC 99-6798-01 Submitted By DILLON CONSULTING LIMITED 130-10691 Shellbridge Way Richmond, B.C. V6X 2W8 IATSE Local 891 Safe Work Procedures for Isocyanate-Containing Products EXECUTIVE SUMMARY Dillon Consulting Limited (Dillon) was retained by I.A.T.S.E. Local 891 to develop safe work procedures to direct film industry personnel in the safe performance of their duties when working with isocyanate-containing products. This document also contains a guideline for minimizing exposure to other individuals in the studio or set that are not working directly with the product. A brief summary of potential routes of exposure and health hazards are outlined as a guideline on how to control the potential for exposure to isocyanate-containing products by the use of engineering controls, administrative controls and personal protective equipment. However, the best method of minimizing exposure to isocyanate products is substituting with less hazardous products. Dillon Consulting Limited IATSE Local 891 Safe Work Procedures for Isocyanate-Containing Products TABLE OF CONTENTS 1.0 INTRODUCTION .......................................................................................................................................1 2.0 ISOCYANATE-CONTAINING PRODUCTS ..........................................................................................1 3.0 POTENTIAL ROUTES OF EXPOSURE AND HEALTH EFFECTS ...................................................1 -
Safety Data Sheet Acc
Page 1/10 Safety Data Sheet acc. to OSHA HCS Printing date 02/27/2020 Reviewed on 09/11/2018 1 Identification · Product identifier · Trade name: Acrylamide/Bis Solution, 37,5:1 · Article number: 10681 · Application of the substance / the mixture Laboratory chemicals · Details of the supplier of the safety data sheet · Manufacturer/Supplier: SERVA Electrophoresis GmbH Carl-Benz-Str. 7 D-69115 Heidelberg Tel.: +49 6221 13840-0 FAX: +49 6221 13840-10 [email protected] · Information department: Product Safety department Tel.: +49 6221 13840-35 · Emergency telephone number: Medical Emergency Information in case of poisoning: Poison Information Center Mainz - Phone: +49 (0) 6131 19240 (advisory service in German or English language) 2 Hazard(s) identification · Classification of the substance or mixture GHS08 Muta. 1B H340 May cause genetic defects. Carc. 1B H350 May cause cancer. Repr. 2 H361 Suspected of damaging fertility or the unborn child. STOT RE 1 H372 Causes damage to organs through prolonged or repeated exposure. GHS07 Acute Tox. 4 H302 Harmful if swallowed. Skin Irrit. 2 H315 Causes skin irritation. Eye Irrit. 2A H319 Causes serious eye irritation. Skin Sens. 1 H317 May cause an allergic skin reaction. · Label elements · GHS label elements The product is classified and labeled according to the Globally Harmonized System (GHS). · Hazard pictograms GHS07, GHS08 · Signal word Danger · Hazard-determining components of labeling: acrylamide N,N'-methylenediacrylamide · Hazard statements Harmful if swallowed. Causes skin irritation. Causes serious eye irritation. May cause an allergic skin reaction. May cause genetic defects. (Contd. on page 2) US 50.0.4 Page 2/10 Safety Data Sheet acc. -
Catalyst for Low Temperature Cure of Blocked Isocyanates
Europaisches Patentamt (19) European Patent Office Office europeen des brevets (11) EP 0 810 245 A1 (12) EUROPEAN PATENT APPLICATION (43) Date of publication: (51) Intel6: C08G 18/24, C08G 18/80, 03.12.1997 Bulletin 1997/49 C08G 63/85, C08G 77/08 (21) Application number: 97108506.3 (22) Date of filing: 27.05.1997 (84) Designated Contracting States: (72) Inventors: AT BE CH DE DK ES Fl FR GB GR IE IT LI LU MC • Gitlitz, Melvin H. NL PT SE Berwyn, PA 1931 2 (US) • Seshadri, Sri R. (30) Priority: 28.05.1996 US 18438 P Newtown, PA 18940 (US) 03.04.1997 US 826603 (74) Representative: (71) Applicant: Kraus, Walter, Dr. et al ELF ATOCHEM NORTH AMERICA, INC. Patentanwalte Kraus, Weisert & Partner Philadelphia, Pennsylvania 19103-3222 (US) Thomas-Wimmer-Ring 15 80539 Munchen (DE) (54) Catalyst for low temperature cure of blocked isocyanates (57) The present invention comprises a polystan- noxane catalyst, a curable composition containing the catalyst and a method of using the catalyst and curing the composition. The curable composition comprises: (i) a blocked isocyanate; (ii) a functional component containing reactive hydrogen; (iii) a polystannoxane catalyst for promoting the reaction of the blocked isocyanate with the func- tional component. A co-catalyst may also be employed based on Cu, Zn, Ni, Zr, Ce, Fe, Co, V, Sb and Bi and especially oxides, salts or chelates of said metals. The invention also relates to a method for curing a blocked isocyanate at a low reaction temperature which comprises combining the catalyst with the blocked isocyanate and functional component and heating to a temperature less than about 180°C to obtain a cured urethane. -
MINI-REVIEW Methyl Isocyanate and Carcinogenesis: Bridgeable Gaps in Scientific Knowledge
DOI:http://dx.doi.org/10.7314/APJCP.2012.13.6.2429 Methyl Isocyanate and Carcinogenesis: Bridgeable Gaps in Scientific Knowledge MINI-REVIEW Methyl Isocyanate and Carcinogenesis: Bridgeable Gaps in Scientific Knowledge Chinnu Sugavanam Senthilkumar1, 2*, Nand Kishore Sah3, Narayanan Ganesh1 Abstract Methyl isocyanate may have a role in cancer etiology, although the link is unclear. There is evidence in the literature that it can induce cancer in animals but the carcinogenic potency is weak. Pheochromocytoma of adrenal medulla and acinar cell tumors of pancreas have been observed in methyl isocyanate exposed animals. Conversely, emerging data from population-based epidemiological studies are contradictory since there is no evidence of such cancers in methyl isocyanate exposed humans. Recently, we reported a high prevalence of breast and lung cancers in such a population in Bhopal. In vitro findings appearing in the latest scientific literature suggest that genomic instability is caused by methyl isocyanate analogs in lung, colon, kidney, ovary epithelial cells, and that hepatocytes may undergo oncogenic transformation, have obvious implications. The conflicting information prompted us to present this update over the last three decades on methyl isocyanate-induced cancers after an extensive literature search using PubMed. While the pertinent literature remains limited, with a scarcity of strong laboratory analyses and field-epidemiological investigations, our succinct review of animal and human epidemiological data including in vitro evidences, should hopefully provide more insight to researchers, toxicologists, and public health professionals concerned with validation of the carcinogenicity of methyl isocyanate in humans. Keywords: Methyl isocyanate - carcinogenicity - need for validation - review Asian Pacific J Cancer Prev, 13, 2429-2435 Introduction recognized the toxicity of MIC in humans. -
Guidelines for Statistical Analysis of Occupational Exposure Data
GUIDELINES FOR STATISTICAL ANALYSIS OF OCCUPATIONAL EXPOSURE DATA FINAL by IT Environmental Programs, Inc. 11499 Chester Road Cincinnati, Ohio 45246-0100 and ICF Kaiser Incorporated 9300 Lee Highway Fairfax, Virginia 22031-1207 Contract No. 68-D2-0064 Work Assignment No. 006 for OFFICE OF POLLUTION PREVENTION AND TOXICS U.S. ENVIRONMENTAL PROTECTION AGENCY 401 M STREET, S.W. WASHINGTON, D.C. 20460 August 1994 DISCLAIMER This report was developed as an in-house working document and the procedures and methods presented are subject to change. Any policy issues discussed in the document have not been subjected to agency review and do not necessarily reflect official agency policy. Mention of trade names or products does not constitute endorsement or recommendation for use. i CONTENTS FIGURES.......................................................... v TABLES........................................................... vi ACKNOWLEDGMENT................................................vii INTRODUCTION.................................................... 1 A. Types of Occupational Exposure Monitoring Data ...................... 1 B. Types of Occupational Exposure Assessments ........................ 2 C. Variability in Occupational Exposure Data ........................... 3 D. Organization of This Report .................................... 4 STEP 1: IDENTIFY USER NEEDS........................................ 9 STEP 2: COLLECT DATA............................................. 15 A. Obtaining Data From NIOSH ................................... 15 -
Center for Dairy Farm Safety - Glossary of Terms
Center for Dairy Farm Safety - Glossary of Terms ACGIH—American Conference of Governmental Industrial Hygienists. A professional organization devoted to worker health protection. In particular, the organization publishes "Threshold Limit Values for Chemical Substances in the Work Environment" and the "Documentation of TLVs." The TLV booklet is one source which may be used in hazard determination. www.acgih.org. ANSI—American National Standards Institute. ANSI is a coordinating body of various trade, technical, professional, and consumer groups who develop voluntary standards. www.ansi.org Acute—An adverse effect on the human body with symptoms of high severity coming quickly to a crisis. Acute effects are normally the result of short term exposures and short duration. Aerosol—This is a solid or liquid particulate, natural or manmade, which can remain suspended in air. Paint spray and smoke are examples of aerosols. Asphyxiant—A chemical, usually in a gas or vapor state, which displaces oxygen or prevents its use in the body by other chemical means. Assistant Secretary (OSHA)—"...means the Assistant Secretary of Labor for Occupational Safety and Health, U.S. Department of Labor, or designee." Autoignition temperature—This is the lowest temperature at which a substance will ignite and sustain combustion in the absence of an ignition source. Blood Agents—These are chemicals such as carbon monoxide and the cyanides which act on the blood and the hematopoietic system and ultimately result in depriving body tissues of adequate oxygen. Boiling point—The temperature at which a liquid changes its physical state to a gas. Toluene has a boiling point of 231°F. -
Explosive Chemical Management Procedures
NMSU EXPLOSIVE CHEMICAL MANAGEMENT PROCEDURES These procedures are a guide to help prevent explosions and protect health and the environment. If you identify old explosives or old organic peroxide forming chemicals, immediately contact Environmental Health and Safety (EH&S) at 646-3327. 1. INTRODUCTION: All explosive chemicals should be identified and carefully managed. There are two main classes of explosive chemicals: 1.1. STANDARD EXPLOSIVE CHEMICALS: These consist of explosive compounds manufactured for detonation such as dynamite, gunpowder, blasting caps, and fireworks. These compounds are rare on the NMSU campus and relatively stable under normal conditions. If these compounds are not being used for a specific, authorized activity they should be immediately called in for pick up by EH&S at 646-3327. 1.2. POTENTIALLY EXPLOSIVE CHEMICALS (PECs): These consist of lab chemicals not intentionally made for detonation but which may explode and/or cause fires if not properly managed. A number of PECs are common on the NMSU campus and should be handled with extra precaution. The main focus of this SOP is to help identify PECs and describe the precautions that should be taken to manage them from purchase through disposal. 2. ORGANIC PEROXIDE FORMING CHEMICALS: This is the principle group of PECs that lead to problems in university labs. They are carbon-based chemicals capable of forming potentially explosive peroxide “O-O” bonds. Below is a breakdown of the four main subcategories of organic peroxide forming chemicals; common ones are specifically identified in the appendices. 2.1. Chemicals that form explosive levels of peroxides without a concentration step, e.g., evaporation, distillation, etc., are listed in Appendix 1. -
Maleic Anhydride
Maleic Anhydride 108-31-6 Hazard Summary Maleic anhydride is used in the formulation of resins. Exposure to maleic anhydride may occur from accidental releases to the environment or in workplaces where it is produced or used. Acute (short-term) inhalation exposure of humans to maleic anhydride has been observed to cause irritation of the respiratory tract and eye irritation. Chronic (long-term) exposure to maleic anhydride has been observed to cause chronic bronchitis, asthma-like attacks, and upper respiratory tract and eye irritation in workers. In some people, allergies have developed so that lower concentrations can no longer be tolerated. Kidney effects were observed in rats chronically exposed to maleic anhydride via gavage (experimentally placing the chemical in the stomach). EPA has not classified maleic anhydride for carcinogenicity. Please Note: The main sources of information for this fact sheet are EPA's Integrated Risk Information System (IRIS) (6), which contains information on oral chronic toxicity and the RfD, and EPA's Health and Environmental Effects Profile for Maleic Anhydride. (2) Other secondary sources include Hazardous Substances Data Bank (HSDB) (1), a database of summaries of peer-reviewed literature, and the Registry of Toxic Effects of Chemical Substances (RTECS) (3), a database of toxic effects that are not peer reviewed. Uses Maleic anhydride is used primarily in the formation of unsaturated polyester resins for use in boats, autos, trucks, buildings, piping, and electrical goods. Lube oil adhesives synthesized from maleic anhydride are used to prolong oil-change intervals and improve engine efficiency. (2,9) Maleic anhydride is also used to make copolymers, pesticides, and other organic compounds, and in Diels-Alder syntheses. -
Technical Data Sheet
Technical Data Sheet PARALOID™ EDGE XL-195 Crosslinker Cycloaliphatic Dialdehyde Description PARALOID™ EDGE XL-195 Crosslinker is a mixture of 1,3 & 1,4- cyclohexanedicarboxaldehyde. It is specifically designed to crosslink with PARALOID EDGE Resins in coating formulations to produce isocyanate-free1, two component (2K) polyurethane systems. Features and • Ambient Cure Benefits • Fast dry time • Long pot-life • Excellent exterior durability • Isocyanate free1 • Excellent adhesion to metal substrates 1 Manufactured without isocyanate Typical Physical Property Typical Values Properties Appearance Liquid Solids (%) >95 Density (lbs/gal) 8.8 Aldehyde Equivalent Weight (EW) – as supplied 70-80 Potential • Industrial Maintenance Finishes for metal Applications • General Industrial Finishes for metal • Agricultural & Construction Equipment (ACE) • Transportation Coatings (e.g., railcar, shipping containers) • Automotive Refinish Coatings (e.g., primer surfacer, topcoat) • Industrial Wood Finishes for Kitchen Cabinets • Industrial Wood Finishes for Furniture • DIY Finishes for Wood • Pigmented or Clear Wood Topcoats UNRESTRICTED – May be shared with anyone ®TM Trademark of The Dow Chemical Company (“Dow”) or an affiliated company of Dow 884-00839-0815-NAR-EN-CDP Page 1 of 3 PARALOIDTM EDGE XL-195 Crosslinker/ Cycloaliphatic Dialdehyde / Dow Coating Materials Introduction to Chemistry and Benefits of PARALOID™ EDGE Isocyanate Free Polyurethane PARALOID™ EDGE Chemistry Technology The PARALOID EDGE Resins and Crosslinkers provide 2K, solvent borne, novel, isocyanate-free polyurethane coatings at ambient temperatures from the reaction of polycarbamate functional resins and polyaldehyde crosslinker using an acid catalyst (Figure 1). There is a need in many coating applications for faster drying and hardness development than can be achieved with current 2K polyurethane chemistry. Typical approaches to faster dry times using isocyanate chemistry can lead to shorter formulation pot-life.