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Merck
CN

347329

(R)-(-)-3-羟基丁酸乙酯

98%

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线性分子式:
CH3CH(OH)CH2CO2C2H5
化学文摘社编号:
分子量:
132.16
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352108
MDL number:
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产品名称

(R)-(-)-3-羟基丁酸乙酯, 98%

InChI

1S/C6H12O3/c1-3-9-6(8)4-5(2)7/h5,7H,3-4H2,1-2H3/t5-/m1/s1

SMILES string

CCOC(=O)C[C@@H](C)O

InChI key

OMSUIQOIVADKIM-RXMQYKEDSA-N

assay

98%

form

liquid

optical activity

[α]20/D −46°, c = 1 in chloroform

optical purity

ee: 99% (GLC)

refractive index

n20/D 1.42 (lit.)

bp

75-76 °C/12 mmHg (lit.)

density

1.017 g/mL at 25 °C (lit.)

functional group

ester
hydroxyl

Quality Level

General description

(R)-3-羟基丁酸乙酯是用于制备在制药行业中所使用的生物活性化合物的一种手性结构单元。它是在聚3-羟基丁酸酯的水解过程中形成的。

存储类别

10 - Combustible liquids

wgk

WGK 3

flash_point_f

147.2 °F - closed cup

flash_point_c

64 °C - closed cup


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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A two-step enzymatic resolution process for large-scale production of (S)-and (R)-ethyl-3-hydroxybutyrate.
Fishman A, et al.
Biotechnology and Bioengineering, 74(3), 256-263 (2001)
Young-Min Han et al.
Molecular cell, 71(6), 1064-1078 (2018-09-11)
β-hydroxybutyrate (β-HB) elevation during fasting or caloric restriction is believed to induce anti-aging effects and alleviate aging-related neurodegeneration. However, whether β-HB alters the senescence pathway in vascular cells remains unknown. Here we report that β-HB promotes vascular cell quiescence, which
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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