|
|
| | 1,4-bis(isocyanatomethyl)cyclohexane Basic information |
| Product Name: | 1,4-bis(isocyanatomethyl)cyclohexane | | Synonyms: | 1,4-bis(isocyanatomethyl)cyclohexane;CYCLOHEXANE,1,4-BIS(ISOCYANATOMETHYL)-;[(1,4-Cyclohexanediyl)bismethylene]diisocyanate;[(Cyclohexane-1,4-diyl)bismethylene]bisisocyanate;1,4-Cyclohexanebis(methylene isocyanate) | | CAS: | 10347-54-3 | | MF: | C10H14N2O2 | | MW: | 194.23 | | EINECS: | 233-757-2 | | Product Categories: | | | Mol File: | 10347-54-3.mol |  |
| | 1,4-bis(isocyanatomethyl)cyclohexane Chemical Properties |
| | 1,4-bis(isocyanatomethyl)cyclohexane Usage And Synthesis |
| Uses | 1,4-Bis(isocyanatomethyl)cyclohexane is a reagent used in the manufacture of poly/thiourethane- optical-based materials.Environmental toxin on US EPA Toxic Release Inventory list (TRI) list. | | 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)]. |
| | 1,4-bis(isocyanatomethyl)cyclohexane Preparation Products And Raw materials |
|