Details:
2,2-Bis(bromomethyl)propane-1,3-diol Basic information |
Product Name: |
2,2-Bis(bromomethyl)propane-1,3-diol |
Synonyms: |
1,3-Dibromo-2,2-dihydroxymethylpropane;1,3-Dibromo-2,2-dimethylolpropane;1,3-Propanediol, 2,2-bis(2-bromomethyl)-;1,3-propanediol,2,2-bis(bromoethyl)-;2,2-Bis(2-bromomethyl)-1,3-propanediol;2,2-bis(bromomethyl)-3-propanediol;2,2-Dibromomethyl-1,3-propanediol;3-Propanediol,2,2-bis(bromomethyl)-1 |
CAS: |
3296-90-0 |
MF: |
C5H10Br2O2 |
MW: |
261.94 |
EINECS: |
221-967-7 |
Product Categories: |
Pharmaceutical Intermediates;Organics;Alcohols;Monomers;Polymer Science;Aliphatics;Mutagenesis Research Chemicals |
Mol File: |
3296-90-0.mol |
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2,2-Bis(bromomethyl)propane-1,3-diol Chemical Properties |
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2,2-Bis(bromomethyl)propane-1,3-diol Usage And Synthesis |
Chemical Properties |
Solid |
Usage |
It is a brominated flame retardant, previously shown to be a multisite carcinogen in experimental animals. , and in rigid polyurethane foam. It shows clear evidence of carcinogenicity and genotoxicity |
General Description |
Off-white powder. |
Air & Water Reactions |
Hygroscopic . Insoluble in water. |
Reactivity Profile |
A brominated alcohol. Flammable and/or toxic gases are generated by the combination of alcohols with alkali metals, nitrides, and strong reducing agents. They react with oxoacids and carboxylic acids to form esters plus water. Oxidizing agents convert them to aldehydes or ketones. Alcohols exhibit both weak acid and weak base behavior. They may initiate the polymerization of isocyanates and epoxides. |
Fire Hazard |
Literature sources indicate that 2,2-Bis(bromomethyl)propane-1,3-diol is nonflammable. |
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2,2-Bis(bromomethyl)propane-1,3-diol Preparation Products And Raw materials |
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