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

trans-2,3-Dibromo-2-butene-1,4-diol Structure
CAS No.
3234-02-4
Chemical Name:
trans-2,3-Dibromo-2-butene-1,4-diol
Synonyms
DBD;Peton22;Penton22;mitolactol;dibromoducitol;2,3-dibromo-2-butene-4-diol;2,3-Dibromo-2-buten-1,4-diol;4-diol,2,3-dibromo-2-Butene-1;2,3-DIBROMO-2-BUTENE-1,4-DIOL;2,3-DIBROMO-1,4-BUT-2-ENEDIOL
CBNumber:
CB8777564
Molecular Formula:
C4H6Br2O2
Molecular Weight:
245.9
MOL File:
3234-02-4.mol
MSDS File:
SDS
Modify Date:
2024/7/25 20:04:51

trans-2,3-Dibromo-2-butene-1,4-diol 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)
pka 11.91±0.10(Predicted)
form Solid:crystalline
Water Solubility 1-5 g/100 mL at 21 ºC
Stability Stable. Incompatible with strong oxidizing agents.
LogP 0.31 at 25℃ and pH7
Surface tension 67.79mN/m at 1g/L and 20℃
CAS DataBase Reference 3234-02-4(CAS DataBase Reference)
EPA Substance Registry System 2,3-Dibromo-2-butene-1,4-diol (3234-02-4)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS07
Signal word  Warning
Hazard statements  H317
Precautionary statements  P280
Hazard Codes  Xi
Risk Statements  36/37/38
Safety Statements  26-37/39
WGK Germany  3
RTECS  EM6910000
Hazard Note  Irritant
HS Code  29055998
NFPA 704
0
1 0

trans-2,3-Dibromo-2-butene-1,4-diol Chemical Properties,Uses,Production

Chemical Properties

white crystalline powder

General Description

Crystals or white powder.

Air & Water Reactions

Water soluble.

Reactivity Profile

A 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 Hazard

Flash 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 materials

Preparation Products

Global( 190)Suppliers
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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 2,3-DIBROMO-2-BUTYLENE-1,4-DIOL 2,3-DIBROMO-1,4-BUT-2-ENEDIOL dibromoducitol mitolactol 2 3-DIBROMO-2-BUTENE-1 4-DIOL 98%(GC) 2,3-Dibromo-2-buten-1,4-diol 2,3-Dibromobut-2-ene-1,4-diol trans-2,3-Dibromo-2-butene-1,4-diol,97% Penton22 Peton22 trans-2,3-DibroMo-2-butene-1,4-diol, 97% 100GR trans-2,3-Dibromo-2-butene-1,4-diol 97% (E)-2,3-Dibromo-2-butene-1,4-diol trans-2,3-Dibromo-2-butene-1,4-diol USP/EP/BP rans-2,3-Dibromo-2-butene-1,4-diol 3234-02-4 3234-2-4 487-27-0 3234/2/4 HOCH2CBrCBrCH2OH Alcohols Monomers Polymer Science