| Weight | 90.122 g/mol |
|---|---|
| Formula | C4H10O2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 2 |
1,2-BUTANEDIOL (584-03-2)
Score:
#1162 in Physics
,
#3313 in Chemistry
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- Present state and perspective of downstream processing of biologically produced 1,3-propanediol and 2,3-butanediol (Applied Microbiology and Biotechnology, 2008)
- Fermentation of glycerol to 1,3-propanediol and 2,3-butanediol by Klebsiella pneumoniae. (Applied Microbiology and Biotechnology, 1998)
- Mutagenicity of butadiene and its epoxide metabolites: I. Mutagenic potential of 1,2-epoxybutene, 1,2,3,4-diepoxybutane and 3,4-epoxy-1,2-butanediol in cultured human lymphoblasts (Carcinogenesis, 1994)
- Synthesis of Enantiomerically Pure -(Menthyloxy)butenolides and (R)- and (S)-2-Methyl-1,4-butanediol (Journal of Organic Chemistry, 1989)
- Production of 1,3-propanediol, 2,3-butanediol and ethanol by a newly isolated Klebsiella oxytoca strain growing on biodiesel-derived glycerol based media (Process Biochemistry, 2012)
- Screening of bacterial strains capable of converting biodiesel-derived raw glycerol into 1,3-propanediol, 2,3-butanediol and ethanol (Engineering in Life Sciences, 2012)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCCC(CO)O
-
InChIKeyBMRWNKZVCUKKSR-UHFFFAOYSA-N
- Pubchem - 1,2-BUTANEDIOL
- Wikipedia - 1,2-butanediol
1,2-Butanediol is a vic-diol (glycol) first described by Charles-Adolphe Wurtz in 1859. It is produced industrially as a byproduct of the production of 1,4-butanediol from butadiene, and is also a byproduct of the catalytic hydrocracking of starches and sugars such as sorbitol to ethylene glycol and propylene glycol. It is used to produce polyester resins and plasticizers, and is a potential feedstock for the industrial production of -ketobutyric acid, a precursor to many amino acids.
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1,2-BUTANEDIOL
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