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ChemicalBook--->CAS DataBase List--->10347-54-3

10347-54-3

10347-54-3 Structure

10347-54-3 Structure
IdentificationBack Directory
[Name]

1,4-bis(isocyanatomethyl)cyclohexane
[CAS]

10347-54-3
[Synonyms]

1,4-bis(isocyanatomethyl)cyclohexane
CYCLOHEXANE,1,4-BIS(ISOCYANATOMETHYL)-
1,4-Cyclohexanebis(methylene isocyanate)
[(1,4-Cyclohexanediyl)bismethylene]diisocyanate
[(Cyclohexane-1,4-diyl)bismethylene]bisisocyanate
[EINECS(EC#)]

233-757-2
[Molecular Formula]

C10H14N2O2
[MOL File]

10347-54-3.mol
[Molecular Weight]

194.23
Chemical PropertiesBack Directory
[Boiling point ]

294℃
[density ]

1.14
[Fp ]

119℃
Safety DataBack Directory
[Symbol(GHS) ]


GHS06
[Signal word ]

Danger
[Hazard statements ]

H330-H302
[Precautionary statements ]

P264-P270-P301+P312-P330-P501-P260-P271-P284-P304+P340-P310-P320-P403+P233-P405-P501
Hazard InformationBack Directory
[Reactivity Profile]

Isocyanates and thioisocyanates, such as 1,4-bis(isocyanatomethyl)cyclohexane , 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)].
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