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L-(+)-2,3-Butanediol

derivatization grade (chiral), LiChropur, ≥97.0%

Synonym(s):

(S,S)-2,3-Butanediol

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About This Item

Empirical Formula (Hill Notation):
C4H10O2
CAS Number:
Molecular Weight:
90.12
Beilstein/REAXYS Number:
1718899
MDL number:
UNSPSC Code:
41116105
PubChem Substance ID:
NACRES:
NA.22

grade

derivatization grade (chiral)

Quality Level

assay

≥97.0% (sum of enantiomers, GC)
≥97.0%

optical activity

[α]20/D +13±1°, neat

optical purity

enantiomeric ratio: ≥99:1 (GC)

quality

LiChropur

technique(s)

HPLC: suitable

refractive index

n20/D 1.433

bp

177-179 °C (lit.)

density

0.992 g/mL at 20 °C (lit.)

storage temp.

2-8°C

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

General description

L-(+)-2,3-Butanediol is a stereoisomer of 2,3-Butanediol (2,3-BD). 2,3-BD may be used in the production of antifreeze solvents, extraction solvents, butadiene, polymers, polyurethane and diacetyl and may also be used as a fuel.[1]

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Legal Information

LiChropur is a trademark of Merck KGaA, Darmstadt, Germany

Storage Class

10 - Combustible liquids

wgk_germany

WGK 3

flash_point_f

185.0 °F - closed cup

flash_point_c

85 °C - closed cup

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter


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Nasib Qureshi, David Hodge, Alain Vertes
Biorefineries: Integrated Biochemical Processes for Liquid Biofuels, 112-112 (2014)
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
Gen Lin Zhang et al.
Biotechnology letters, 34(8), 1519-1523 (2012-05-02)
The budC gene encoding the meso-2,3-BDH from Klebsiella pneumoniae XJ-Li was expressed in E. coli BL21 (DE3) pLys. Hypothetical amino acid sequence alignments revealed that the enzyme belongs to the short chain dehydrogenase/reductase family. After purification and refolding, the recombinant
Hyun-Dong Shin et al.
Bioresource technology, 118, 367-373 (2012-06-19)
Escherichia coli has been engineered to produce a variety of biofuel and biorefinery products. However, it can only produce these products from simple sugars, requiring large amounts of enzymes to depolymerize cellulose into monomer sugars. Engineering E. coli to directly
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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