TRIMETHYL-1,6-HEXAMETHYLENE DIISOCYANATE
TRIMETHYL-1,6-HEXAMETHYLENE DIISOCYANATE Basic information
- Product Name:
- TRIMETHYL-1,6-HEXAMETHYLENE DIISOCYANATE
- Synonyms:
-
- 1,6-diisocyanato-2,4,4-trimethyl-hexan
- 1,6-diisocyanato-2,4,4-trimethyl-Hexane
- 2,4,4-trimethylhexa-1,6-diyl diisocyanate
- 2,4,4-Trimethyl-1,6-diisocyanatohexane
- 2,4,4-trimethylhexamethylenediisocyanate
- TRIMETHYL-1,6-HEXAMETHYLENE DIISOCYANATE
- HEXANE,1,6-DIISOCYANATO-2,4,4-TRIMETHYL-
- 2,4,4- Trimethylcyclohexamethylen-1,6-diisocyanat
- CAS:
- 15646-96-5
- MF:
- C11H18N2O2
- MW:
- 210.27
- EINECS:
- 239-714-4
- Mol File:
- 15646-96-5.mol
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TRIMETHYL-1,6-HEXAMETHYLENE DIISOCYANATE Chemical Properties
- Boiling point:
- 283.8±23.0 °C(Predicted)
- Density
- 0.97±0.1 g/cm3(Predicted)
- EPA Substance Registry System
- 2,4,4-Trimethylhexamethylene diisocyanate (15646-96-5)
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TRIMETHYL-1,6-HEXAMETHYLENE DIISOCYANATE Usage And Synthesis
Reactivity Profile
Isocyanates and thioisocyanates, such as TRIMETHYL-1,6-HEXAMETHYLENE DIISOCYANATE, 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)].