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The isocyanate functional group. In organic chemistry, isocyanate is the functional group with the formula R−N=C=O. Organic compounds that contain an isocyanate group are referred to as isocyanates. An organic compound with two isocyanate groups is known as a diisocyanate.
This is the list of extremely hazardous substances defined in Section 302 of the U.S. Emergency Planning and Community Right-to-Know Act (42 U.S.C. § 11002). The list can be found as an appendix to 40 CFR 355. [1] Updates as of 2006 can be seen on the Federal Register, 71 FR 47121 (August 16, 2006). [2]
Methyl isocyanate (MIC) is an organic compound with the molecular formula CH 3 NCO. Synonyms are isocyanatomethane and methyl carbylamine . Methyl isocyanate is an intermediate chemical in the production of carbamate pesticides and Haffmann Bromamide Degradation (such as carbaryl , carbofuran , methomyl , and aldicarb ).
An isocyanate at the 4-position is approximately four times more reactive than the group at the 2-position due to steric hindrance. [4] In 4,4′-MDI and 2,2′-MDI, the two isocyanate groups are equivalent to each other, but in 2,4′-MDI the two groups display highly differing reactivities. MDI isomers and polymer
The molecule consists of a phenyl ring attached to the isocyanate functional group. It is a colourless liquid that reacts with water. Phenyl isocyanate has a strong odor and tearing vapours, therefore it has to be handled with care. Characteristic of other isocyanates, it reacts with amines to give ureas. [2]
The NA numbers (North American Numbers are assigned by the United States Department of Transportation, supplementing the larger set of UN numbers, for identifying hazardous materials. NA numbers largely duplicate UN numbers, however a selection of additional numbers are provided for materials that are not covered by UN numbers as a hazardous ...
A highly hazardous chemical, also called a harsh chemical, is a substance classified by the American Occupational Safety and Health Administration as material that is both toxic and reactive and whose potential for human injury is high if released. Highly hazardous chemicals may cause cancer, birth defects, induce genetic damage, cause ...
At least 3 companies sell material in this form commercially. It is also used as an activator in process of in situ polymerization of caprolactam i.e. cast nylon process. HDI is also used bisoxazolidine synthesis as the hydroxyl group on the molecule allows for further reaction with hexamethylene diisocyanate. [7] [8]