300349
(2S,3S)-(+)-2,3-Butanediol
97%
Synonym(s):
(+)-2,3-Butanediol, (2S,3S)-2,3-Butanediol, (S,S)-2,3-Butanediol, Dextro-2,3-Butanediol, L-(+)-Butane-2,3-diol
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500 MG
€98.50
1 G
€121.00
5 G
€394.00
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500 MG
€98.50
1 G
€121.00
5 G
€394.00
About This Item
Linear Formula:
CH3CH(OH)CH(OH)CH3
CAS Number:
Molecular Weight:
90.12
Beilstein:
1718899
MDL number:
UNSPSC Code:
12352001
PubChem Substance ID:
NACRES:
NA.22
form:
liquid
Assay:
97%
Recommended Products
Quality Level
Assay
97%
form
liquid
optical activity
[α]20/D +13°, neat
optical purity
ee: 99% (GLC)
refractive index
n20/D 1.433 (lit.)
bp
179-182 °C (lit.)
density
0.987 g/mL at 25 °C (lit.)
functional group
hydroxyl
SMILES string
C[C@H](O)[C@H](C)O
InChI
1S/C4H10O2/c1-3(5)4(2)6/h3-6H,1-2H3/t3-,4-/m0/s1
InChI key
OWBTYPJTUOEWEK-IMJSIDKUSA-N
Related Categories
General description
(2S,3S)-2,3-Butanediol ((2S,3S)-2,3-BD) is a chiral compound that can be used as a building block in organic synthesis for the preparation of bioactive molecules.[1]
Storage Class Code
10 - Combustible liquids
WGK
WGK 3
Flash Point(F)
185.0 °F - closed cup
Flash Point(C)
85 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Biocatalytic production of (2S, 3S)-2, 3-butanediol from diacetyl using whole cells of engineered Escherichia coli
Li L, et al.
Bioresource Technology, 115, 111-116 (2012)
Yuansheng Xue et al.
Sheng wu gong cheng xue bao = Chinese journal of biotechnology, 27(12), 1742-1748 (2012-04-18)
The production of 2, 3-butanediol and succinic acid by a moderate halophile under anaerobic condition was investigated. This halophile, termed Salinivibrio YS, was isolated from the solid samples collected from Aydingkol Lake. Based on the single factor experiment, the parameters
Mingshou Lu et al.
Journal of microbiology and biotechnology, 22(5), 659-667 (2012-05-09)
2,3-Butanediol (2,3-BDO) is an organic compound with a wide range of industrial applications. Although Escherichia coli is often used for the production of organic compounds, the wild-type E. coli does not contain two essential genes in the 2,3-BDO biosynthesis pathway
Jinshan Li et al.
Applied microbiology and biotechnology, 97(2), 585-597 (2012-08-07)
Paenibacillus polymyxa can produce the (R,R)-stereoisomer of 2,3-butanediol (2,3-BDL) which is industrially very useful. Two important factors affecting (R,R)-BDL production by P. polymyxa ATCC 12321, medium composition, and addition of acetic acid to the culture were investigated in this study
Xiaolin Shen et al.
Journal of industrial microbiology & biotechnology, 39(11), 1725-1729 (2012-07-27)
This work describes the production of (R,R)-2,3-butanediol in Escherichia coli using glycerol by metabolic engineering approaches. The introduction of a synthetic pathway converting pyruvate to (R,R)-2,3-butanediol into wild-type E. coli strain BW25113 led to the production of (R,R)-2,3-butanediol at a
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