5-(p-isocyanatobenzyl)-o-tolyl isocyanate

5-(p-isocyanatobenzyl)-o-tolyl isocyanate Basic information
Product Name:5-(p-isocyanatobenzyl)-o-tolyl isocyanate
Synonyms:5-(p-isocyanatobenzyl)-o-tolyl isocyanate;BENZENE,2-ISOCYANATO-4-((4-ISOCYANATOPHENYL)METHYL)-1-MET.;2-Isocyanato-4-[(4-isocyanatophenyl)methyl]-1-methylbenzene
CAS:75790-84-0
MF:C16H12N2O2
MW:264.27868
EINECS:278-312-3
Product Categories:
Mol File:75790-84-0.mol
5-(p-isocyanatobenzyl)-o-tolyl isocyanate Structure
5-(p-isocyanatobenzyl)-o-tolyl isocyanate Chemical Properties
EPA Substance Registry System4-Methyldiphenylmethane-3,4-diisocyanate (75790-84-0)
Safety Information
MSDS Information
5-(p-isocyanatobenzyl)-o-tolyl isocyanate Usage And Synthesis
Uses5-?(p-?Isocyanatobenzyl)?-?O-?tolyl Isocyanate is used in the manufacture of polyurethanes.Environmental toxin on US EPA Toxic Release Inventory list (TRI) list.
Reactivity ProfileIsocyanates and thioisocyanates, such as 5-(p-isocyanatobenzyl)-o-tolyl isocyanate, are incompatible with many classes of compounds, reacting exothermically to release toxic gases. Reactions with amines, aldehydes, alcohols, alkali metals, ketones, mercaptans, strong oxidizers, hydrides, phenols, and peroxides can cause vigorous releases of heat. Acids and bases initiate polymerization reactions in these materials. Some isocyanates react with water to form amines and liberate carbon dioxide. Base-catalysed reactions of isocyanates with alcohols should be carried out in inert solvents. Such reactions in the absence of solvents often occur with explosive violence, [Wischmeyer(1969)].
5-(p-isocyanatobenzyl)-o-tolyl isocyanate Preparation Products And Raw materials
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