Methylene Bisphenyl Isocyanate Hazard

Total Page:16

File Type:pdf, Size:1020Kb

Methylene Bisphenyl Isocyanate Hazard Common Name: METHYLENE BISPHENYL ISOCYANATE CAS Number: 101-68-8 DOT Number: UN 2489 RTK Substance number: 1253 DOT Hazard Class: 6.1 (Poison) Date: June 1998 Revision: March 2006 ------------------------------------------------------------------------- ------------------------------------------------------------------------- HAZARD SUMMARY * Methylene Bisphenyl Isocyanate can affect you when * Exposure to hazardous substances should be routinely breathed in. evaluated. This may include collecting personal and area * Methylene Bisphenyl Isocyanate can irritate the skin air samples. You can obtain copies of sampling results causing a rash or burning feeling on contact. from your employer. You have a legal right to this * Breathing Methylene Bisphenyl Isocyanate can irritate information under the OSHA Access to Employee the nose, throat and lungs. Exposure and Medical Records Standard (29 CFR * Methylene Bisphenyl Isocyanate may cause a skin 1910.1020). allergy. If allergy develops, very low future exposure can * If you think you are experiencing any work-related health cause itching and a skin rash. problems, see a doctor trained to recognize occupational diseases. Take this Fact Sheet with you. * Methylene Bisphenyl Isocyanate may cause an asthma- like allergy. Future exposure can cause asthma attacks with shortness of breath, wheezing, cough, and/or chest WORKPLACE EXPOSURE LIMITS tightness. OSHA: The legal airborne permissible exposure limit (PEL) is 0.02 ppm, not to be exceeded at any IDENTIFICATION time. Methylene Bisphenyl Isocyanate is an odorless, white to light-yellow, flake-like solid. It is used to manufacture NIOSH: The recommended airborne exposure limit is Polyurethane foams. 0.005 ppm averaged over a 10-hour workshift and 0.02 ppm, not to be exceeded during any REASON FOR CITATION 10- minute work period. * Methylene Bisphenyl Isocyanate is on the Hazardous ACGIH: The recommended airborne exposure limit is Substance List because it is regulated by OSHA and cited 0.005 ppm averaged over an 8-hour workshift. by ACGIH, DOT, NIOSH, DEP, IARC, IRIS and EPA. * Definitions are provided on page 5. WAYS OF REDUCING EXPOSURE HOW TO DETERMINE IF YOU ARE BEING * Where possible, enclose operations and use local exhaust ventilation at the site of chemical release. If local exhaust EXPOSED ventilation or enclosure is not used, respirators should be The New Jersey Right to Know Act requires most employers worn. to label chemicals in the workplace and requires public * Wear protective work clothing. employers to provide their employees with information and * Wash thoroughly immediately after exposure to training concerning chemical hazards and controls. The Methylene Bisphenyl Isocyanate and at the end of the federal OSHA Hazard Communication Standard (29 CFR workshift. 1910.1200) requires private employers to provide similar * Post hazard and warning information in the work area. In training and information to their employees. addition, as part of an ongoing education and training effort, communicate all information on the health and safety hazards of Methylene Bisphenyl Isocyanate to potentially exposed workers. METHYLENE BISPHENYL ISOCYANATE page 2 of 6 This Fact Sheet is a summary source of information of all If symptoms develop or overexposure is suspected, the potential and most severe health hazards that may result from following are recommended: exposure. Duration of exposure, concentration of the substance and other factors will affect your susceptibility to any of the * Evaluation by a qualified allergist, including careful potential effects described below. exposure history and special testing, may help diagnose -------------------------------------------------------------------------- skin allergy. * Chest x-ray and lung function tests. HEALTH HAZARD INFORMATION Any evaluation should include a careful history of past and Acute Health Effects present symptoms with an exam. Medical tests that look for The following acute (short-term) health effects may occur damage already done are not a substitute for controlling immediately or shortly after exposure to Methylene Bisphenyl exposure. Isocyanate: Request copies of your medical testing. You have a legal right * Methylene Bisphenyl Isocyanate can irritate the skin to this information under the OSHA Access to Employee causing a rash or burning feeling on contact. Exposure and Medical Records Standard (29 CFR 1910.1020). * Breathing Methylene Bisphenyl Isocyanate can irritate the nose, throat and lungs. Mixed Exposures * Because smoking can cause heart disease, as well as lung Chronic Health Effects cancer, emphysema, and other respiratory problems, it may The following chronic (long-term) health effects can occur at worsen respiratory conditions caused by chemical exposure. some time after exposure to Methylene Bisphenyl Isocyanate Even if you have smoked for a long time, stopping now will and can last for months or years: reduce your risk of developing health problems. Cancer Hazard Conditions Made Worse By Exposure * While Methylene Bisphenyl Isocyanate has been tested, it * Persons with asthma may be at increased risk of health is not classifiable as to its potential to cause cancer. effects from exposure to Methylene Bisphenyl Isocyanate. Reproductive Hazard WORKPLACE CONTROLS AND PRACTICES * According to the information presently available to the New Jersey Department of Health and Senior Services, Unless a less toxic chemical can be substituted for a hazardous Methylene Bisphenyl Isocyanate has not been tested for substance, ENGINEERING CONTROLS are the most its ability to affect reproduction. effective way of reducing exposure. The best protection is to enclose operations and/or provide local exhaust ventilation at Other Long-Term Effects the site of chemical release. Isolating operations can also * Methylene Bisphenyl Isocyanate may cause a skin allergy. reduce exposure. Using respirators or protective equipment is If allergy develops, very low future exposure can cause less effective than the controls mentioned above, but is itching and a skin rash. sometimes necessary. * Methylene Bisphenyl Isocyanate may cause an asthma- like allergy. Future exposure can cause asthma attacks with In evaluating the controls present in your workplace, consider: shortness of breath, wheezing, cough, and/or chest (1) how hazardous the substance is, (2) how much of the tightness. substance is released into the workplace and (3) whether * Repeated allergic lung attacks may lead to permanent harmful skin or eye contact could occur. Special controls scarring of the lungs (pulmonary fibrosis), with reduced should be in place for highly toxic chemicals or when lung function. significant skin, eye, or breathing exposures are possible. MEDICAL In addition, the following control is recommended: * Where possible, automatically transfer Methylene Medical Testing Bisphenyl Isocyanate from drums or other storage Before beginning employment and at regular times after that, containers to process containers. the following are recommended: Good WORK PRACTICES can help to reduce hazardous * Lung function tests. These may be normal if the person is exposures. The following work practices are recommended: not having an attack at the time of the test. * Workers whose clothing has been contaminated by Methylene Bisphenyl Isocyanate should change into clean clothing promptly. METHYLENE BISPHENYL ISOCYANATE page 3 of 6 * Do not take contaminated work clothes home. Family Respiratory Protection members could be exposed. IMPROPER USE OF RESPIRATORS IS DANGEROUS. * Contaminated work clothes should be laundered by Such equipment should only be used if the employer has a individuals who have been informed of the hazards of written program that takes into account workplace conditions, exposure to Methylene Bisphenyl Isocyanate. requirements for worker training, respirator fit testing, and * Eye wash fountains should be provided in the immediate medical exams, as described in the OSHA Respiratory work area for emergency use. Protection Standard (29 CFR 1910.134). * If there is the possibility of skin exposure, emergency shower facilities should be provided. * Where the potential exists for exposure over 0.005 ppm, * On skin contact with Methylene Bisphenyl Isocyanate, use a NIOSH approved supplied-air respirator with a full immediately wash or shower to remove the chemical. At facepiece operated in a pressure-demand or other positive- the end of the workshift, wash any areas of the body that pressure mode. For increased protection use in combination may have contacted Methylene Bisphenyl Isocyanate, with an auxiliary self-contained breathing apparatus whether or not known skin contact has occurred. operated in a pressure-demand or other positive-pressure * Do not eat, smoke, or drink where Methylene Bisphenyl mode. Isocyanate is handled, processed, or stored, since the * Exposure to 7.3 ppm is immediately dangerous to life and chemical can be swallowed. Wash hands carefully before health. If the possibility of exposure above 7.3 ppm exists, eating, drinking, applying cosmetics, smoking, or using the use a NIOSH approved self-contained breathing apparatus toilet. with a full facepiece operated in a pressure-demand or other * Use a vacuum or a wet method to reduce dust during clean- positive-pressure mode. up. DO NOT DRY SWEEP. HANDLING AND STORAGE PERSONAL PROTECTIVE EQUIPMENT * Prior to working with Methylene Bisphenyl Isocyanate WORKPLACE CONTROLS ARE BETTER THAN you should be trained on its proper handling
Recommended publications
  • 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
    [Show full text]
  • 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
    [Show full text]
  • 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.
    [Show full text]
  • 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.
    [Show full text]
  • 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.
    [Show full text]
  • 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.
    [Show full text]
  • Isocyanates November 2010 Information Sheet
    Isocyanates November 2010 Information Sheet Isocyanate compounds are found in a diverse range of industries using chemicals such as two pack spray paints, lacquers, adhesives, certain coatings/ linings and in foam production, such as insulation or fillers. Industries also include motor vehicle repair, printing (inks, framing and laminating), boat maintenance or furniture manufacture. The most widely used isocyanates are TDI (toluene di-isocyanate), MDI (methylene diphenyl di-isocyanate) and HDI (hexamethylene di-isocyanate). Routes of Exposure • Skin sensitisation can occur due to the irritant nature of isocyanates in contact with the skin surface, which Isocyanates enter the body primarily through inhalation may result in dermatitis. or skin exposure. For example, polyurethane foam production results from the generation of gas, e.g. carbon dioxide which can promote the release of Occupational Exposure Limits isocyanates as vapour/aerosols. There is an Occupational Exposure Limit Value (OELV) for all Isocyanates of 0.02mg/m 3 (8hr); 0.07mg/m 3 (15 Health Effects minute) except Toluene di-isocyanate which is There are several potential health effects associated with 0.001mg/m 3 (8hr); 0.003mg/m 3 (15 minute). As a result, exposure to isocyanates. Some examples are provided employers must reduce employee’s exposure as far as is below: reasonably practicable and not exceed the OELV. • Inhalation of isocyanates can cause respiratory irritation/sensitisation in people or lead to occupational asthma. Individuals with a history of asthma should not work in areas with the potential for isocyanate exposure. Isocyanates Information Sheet Recommended Control Measures Key Points • Employers should firstly consider elimination of Always assume that exposure is likely to occur and isocyanates or substitution with less hazardous protect according to the level of risk identified from risk alternatives.
    [Show full text]
  • Synthesis and Thermotropic Properties of Polyurethanes Prepared from 2,5-Tolylene Diisocyanate and 2,6-Bis(W-Hydroxyalkoxy )Naphthalenes
    Polymer Journal, Vol. 27, No. 7, pp 664-672 (1995) Synthesis and Thermotropic Properties of Polyurethanes Prepared from 2,5-Tolylene Diisocyanate and 2,6-Bis(w-hydroxyalkoxy )naphthalenes Jong Back LEE, Takashi KATO, and Toshiyuki URYU* Institute of Industrial Science, University of Tokyo, Roppongi, Minato-ku, Tokyo 106, Japan (Received October 12, 1994) ABSTRACT: A series of thermotropic polyurethanes containing no mesogenic unit were synthesized by polyaddition of a para-type diisocyanate such as 2,5-tolylene diisocyanate (2,5-TDI) with 2,6-bis(w-hydroxyalkoxy)naphthalenes (BHNm: HO(CH2 )mOC10H 6 O(CH2 )mOH; m is the carbon number in the hydroxyalkoxy group). Intrinsic viscosities of the polymers were in the range of 0.27---0.48 dL g- 1. The thermal properties of these polymers were studied by differential scan­ ning calorimetry, thermogravimetric analysis, polarizing microscopy, and X-ray diffractometry. Polyurethane 2,5-TDI/BHNm's (m=5, 6, 8, 11) prepared from BHNm and 2,5-TDI having methyl substituent on the phenylene unit exhibited monotropic liquid crystallinity. For example, poly­ urethane 2,5-TDI/BHN8 with [IJ]=0.30 exhibited a mesophase from 139 to lll°C on cooling. However, in the series of polyurethanes prepared by polycondensation of 1,4-phenylene di­ isocyanate (1,4-PDI) with BHNm, no explicit mesomorphic behavior was observed by DSC measurement and polarizing microscopic observation. KEY WORDS Thermotropic Polyurethane / 2,5-Tolylene Diisocyanate / 1,4-Phenylene Diisocyanate / Hydrogen Bonding/ Polyurethanes are a distinct class of mate­ In the previous paper, we reported the syn­ rials with industrial importance.
    [Show full text]
  • Isocyanate Hazard in Spray Finishing Operations Loss Prevention Safety Topics
    LOSS PREVENTION SAFETY TOPICS ISOCYANATE HAZARD IN SPRAY FINISHING OPERATIONS LOSS PREVENTION SAFETY TOPICS Isocyanate Hazard in Spray Finishing Operations The use of urethane paints and coatings in spray finishing operations has increased dramatically over recent years. The materials consist of two parts: a Isocyanates present both acute urethane-based resin, and an isocyanate catalyst. During the spray finishing operation, the resin and isocyanate catalyst are combined to form a durable and chronic occupational weather and moisture-resistant finish. The isocyanates most commonly disease exposures. found in these two-part paints and coating systems are methylene bisphenyl isocyanate (MDI) and toluene diisocyanate (TDI). Isocyanates present both acute and chronic occupational disease exposures. Acute effects include shortness of breath, tightness of chest, nausea, eye irritation, skin irritation, dizziness, and abdominal pains. In cases of massive exposure, loss of consciousness, accumulation of water in the lungs, and asphyxiation can occur. Chronic or longterm effects include damage to the respiratory system and sensitization. Once a person becomes sensitized to isocyanate, subsequent exposure to even minute quantities can trigger asthmatic-like reactions, which make the individual unable to work with, or come in contact with, any products containing isocyanate. Workers’ Compensation claim costs resulting from isocyanate sensitization are usually very high. The primary worker exposure to isocyanate occurs during spray application, when droplets of the urethane paint or coating containing isocyanate become airborne. The paint or coating mixing operation can also add to the worker’s exposure. The current Occupational Safety and Health Administration (OSHA) Permissible Exposure Limit (PEL) for isocyanate is 0.02 parts per million (ppm).
    [Show full text]
  • Isocyanate Component A
    SAFETY DATA SHEET Isocyanate Component A SECTION 1: Identification of the substance/mixture and of the company/undertaking 1.1 Product identifier Trade name : Isocyanate Component A Substance name : Isocyanic acid, polymethylenepolyphenylene ester 1.2 Relevant identified uses of the substance or mixture and uses advised against Use of the : Component of a Polyurethane System. Substance/Mixture Uses advised against : Professional use of aprotic polar solvents for cleaning., Consumer spray applications., Consumer products requiring heating above 40°C. 1.3 Details of the supplier of the safety data sheet Company : 3315 E Division St Address : Arlington, Texas 76017 Telephone : 817-640-4900 E-mail address of person : [email protected] responsible for the SDS 1.4 Emergency telephone number Emergency telephone number : In USA, call Chemtrec at (800) 424-9300. In Canada, call Canutec at (613) 966-6666, 1 / 21 SAFETY DATA SHEET Isocyanate Component A SECTION 2: Hazards identification 2.1 Classification of the substance or mixture Classification (REGULATION (EC) No 1272/2008) Acute toxicity, Category 4 H332: Harmful if inhaled. Skin irritation, Category 2 H315: Causes skin irritation. Eye irritation, Category 2 H319: Causes serious eye irritation. Respiratory sensitisation, Category 1 H334: May cause allergy or asthma symptoms or breathing difficulties if inhaled. Skin sensitisation, Category 1 H317: May cause an allergic skin reaction. Carcinogenicity, Category 2 H351: Suspected of causing cancer. Specific target organ toxicity - single H335: May cause respiratory irritation. exposure, Category 3, Respiratory system Specific target organ toxicity - repeated H373: May cause damage to organs through exposure, Category 2 prolonged or repeated exposure. 2.2 Label elements Labelling (REGULATION (EC) No 1272/2008) Hazard pictograms : Signal word : Danger Hazard statements : H315 Causes skin irritation.
    [Show full text]
  • Environmental Health Criteria 242
    INTERNATIONAL PROGRAMME ON CHEMICAL SAFETY Environmental Health Criteria 242 DERMAL EXPOSURE IOMC INTER-ORGANIZATION PROGRAMME FOR THE SOUND MANAGEMENT OF CHEMICALS A cooperative agreement among FAO, ILO, UNDP, UNEP, UNIDO, UNITAR, WHO, World Bank and OECD This report contains the collective views of an international group of experts and does not necessarily represent the decisions or the stated policy of the World Health Organization The International Programme on Chemical Safety (IPCS) was established in 1980. The overall objec- tives of the IPCS are to establish the scientific basis for assessment of the risk to human health and the environment from exposure to chemicals, through international peer review processes, as a prerequi- site for the promotion of chemical safety, and to provide technical assistance in strengthening national capacities for the sound management of chemicals. This publication was developed in the IOMC context. The contents do not necessarily reflect the views or stated policies of individual IOMC Participating Organizations. The Inter-Organization Programme for the Sound Management of Chemicals (IOMC) was established in 1995 following recommendations made by the 1992 UN Conference on Environment and Development to strengthen cooperation and increase international coordination in the field of chemical safety. The Participating Organizations are: FAO, ILO, UNDP, UNEP, UNIDO, UNITAR, WHO, World Bank and OECD. The purpose of the IOMC is to promote coordination of the policies and activities pursued by the Participating Organizations, jointly or separately, to achieve the sound management of chemicals in relation to human health and the environment. WHO Library Cataloguing-in-Publication Data Dermal exposure. (Environmental health criteria ; 242) 1.Hazardous Substances - poisoning.
    [Show full text]
  • EPA's Hazardous Waste Listing
    Hazardous Waste Listings A User-Friendly Reference Document September 2012 Table of Contents Introduction ..................................................................................................................................... 3 Overview of the Hazardous Waste Identification Process .............................................................. 5 Lists of Hazardous Wastes .............................................................................................................. 5 Summary Chart ............................................................................................................................... 8 General Hazardous Waste Listing Resources ................................................................................. 9 § 261.11 Criteria for listing hazardous waste. .............................................................................. 11 Subpart D-List of Hazardous Wastes ............................................................................................ 12 § 261.31 Hazardous wastes from non-specific sources. ............................................................... 13 Spent solvent wastes (F001 – F005) ......................................................................................... 13 Wastes from electroplating and other metal finishing operations (F006 - F012, and F019) ... 18 Dioxin bearing wastes (F020 - F023, and F026 – F028) .......................................................... 22 Wastes from production of certain chlorinated aliphatic hydrocarbons (F024
    [Show full text]