trans-2,3-Dibromo-2-butene-1,4-diol

trans-2,3-Dibromo-2-butene-1,4-diol Basic information
Product Name:trans-2,3-Dibromo-2-butene-1,4-diol
Synonyms:2,3-dibromo-2-butene-4-diol;4-diol,2,3-dibromo-2-Butene-1;TRANS-2,3-DIBROMO-1,4-DIHYDROXY-2-BUTENE;TRANS-2,3-DIBROMO-2-BUTENE-1,4-DIOL;TRANS-2,3-DIBROMO-2-BUTEN-1,4-DIOL;DBD;DIBROMO(-2,3)-2-BUTENE-1,4-DIOL;2,3-DIBROMO-2-BUTENE-1,4-DIOL
CAS:3234-02-4
MF:C4H6Br2O2
MW:245.9
EINECS:221-779-5
Product Categories:Alcohols;Monomers;Polymer Science
Mol File:3234-02-4.mol
trans-2,3-Dibromo-2-butene-1,4-diol Structure
trans-2,3-Dibromo-2-butene-1,4-diol Chemical Properties
Melting point 112-114 °C(lit.)
Boiling point 318.1±42.0 °C(Predicted)
density 1.9671 (rough estimate)
vapor pressure 0.004-0.081Pa at 25-40℃
refractive index 1.5230 (estimate)
pka11.91±0.10(Predicted)
form Solid:crystalline
Water Solubility 1-5 g/100 mL at 21 ºC
Stability:Stable. Incompatible with strong oxidizing agents.
LogP0.31 at 25℃ and pH7
Surface tension67.79mN/m at 1g/L and 20℃
CAS DataBase Reference3234-02-4(CAS DataBase Reference)
EPA Substance Registry System2,3-Dibromo-2-butene-1,4-diol (3234-02-4)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-37/39
WGK Germany 3
RTECS EM6910000
Hazard Note Irritant
HS Code 29055998
MSDS Information
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trans-2,3-Dibromo-2-butene-1,4-diol English
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trans-2,3-Dibromo-2-butene-1,4-diol Usage And Synthesis
Chemical Propertieswhite crystalline powder
General DescriptionCrystals or white powder.
Air & Water ReactionsWater soluble.
Reactivity ProfileA halogenated alkene and alcohol. The unsaturated aliphatic hydrocarbons are generally much more reactive than the alkanes, which are saturated aliphatic hydrocarbons. Strong oxidizers may react vigorously with them. Reducing agents can react exothermically to release gaseous hydrogen. 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 HazardFlash point data for trans-2,3-Dibromo-2-butene-1,4-diol are not available, however trans-2,3-Dibromo-2-butene-1,4-diol is probably combustible.
trans-2,3-Dibromo-2-butene-1,4-diol Preparation Products And Raw materials
Raw materials2-Butyne-1,4-diol
Preparation Products3,4-DIBROMOFURAN
Bendamustine TRANS-2,3-DIBROMO-2-BUTENE-1,4-DIOL 2-Methylsuccinic acid 2-Butene-1,4-diol 3-BUTENE-1,2-DIOL 3-BUTENE-1,2-DIOL 2,3-DIBROMO-2-BUTENE-1,4-DIOL = TRANS-2,3-DIBROMO-2-BUTENE-1,4-DIOL 3-BUTENE-1,2-DIOL 2-Butene-1,4-diol

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