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About This Item
Linear Formula:
CH3CH(OH)CH2CO2CH3
CAS Number:
Molecular Weight:
118.13
UNSPSC Code:
12352108
NACRES:
NA.22
PubChem Substance ID:
EC Number:
223-610-0
Beilstein/REAXYS Number:
6130687
MDL number:
Assay:
99%
InChI key
LDLDJEAVRNAEBW-SCSAIBSYSA-N
InChI
1S/C5H10O3/c1-4(6)3-5(7)8-2/h4,6H,3H2,1-2H3/t4-/m1/s1
SMILES string
COC(=O)C[C@@H](C)O
assay
99%
optical activity
[α]20/D −19.5°, neat
optical purity
ee: 98% (GLC)
refractive index
n20/D 1.421 (lit.)
bp
56-58 °C/11 mmHg (lit.)
density
1.055 g/mL at 20 °C (lit.)
functional group
ester, hydroxyl
storage temp.
2-8°C
Quality Level
Related Categories
Application
Methyl (R)-3-hydroxybutyrate may be used in the preparation of (R)-(-)-3-hydroxybutanoic acid and poly-(R)-(-)-3-hydroxybutyrate.
Optically active starting material
Packaging
Bottomless glass bottle. Contents are inside inserted fused cone.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
wgk
WGK 3
Storage Class
10 - Combustible liquids
flash_point_f
163.4 °F - closed cup
flash_point_c
73 °C - closed cup
ppe
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
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Synthesis of biodegradable polyesters by polycondensation of methyl (R)-3-hydroxybutyrate and methyl (R)-3-hydroxy-valerate.
Kobayashi T, et al.
Makromol. Chem., Rapid Commun., 14(12), 785-790 (1993)
Direct Degradation of the Biopolymer Poly [(R)-3-Hydroxybutyric Acid] to (R)-3-Hydroxybutanoic Acid and its Methyl Ester.
Seebach D, et al.
Organic Syntheses, 39-39 (1992)
Diya Alsafadi et al.
New biotechnology, 34, 47-53 (2016-05-26)
Olive mill wastewater (OMW), a highly polluting waste from the olive oil industry, was utilized as sole carbon source for the production of polyhydroxyalkanoate (PHA) by extremely halophilic Haloferax Mediterranei (H. mediterranei) in a one stage cultivation step. H. mediterranei
Xiao-Hong Chen et al.
PloS one, 9(4), e94543-e94543 (2014-04-18)
A novel carbonyl reductase (AcCR) catalyzing the asymmetric reduction of ketones to enantiopure alcohols with anti-Prelog stereoselectivity was found in Acetobacter sp. CCTCC M209061 and enriched 27.5-fold with an overall yield of 0.4% by purification. The enzyme showed a homotetrameric
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