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Merck
CN

230340

L-(-)-乳酸甲酯

greener alternative

98%, optical purity ee: 97% (GLC)

别名:

(S)-(-)-乳酸甲酯

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关于此项目

线性分子式:
CH3CH(OH)CO2CH3
化学文摘社编号:
分子量:
104.10
UNSPSC Code:
12352108
NACRES:
NA.22
PubChem Substance ID:
EC Number:
248-704-9
Beilstein/REAXYS Number:
1720587
MDL number:
Assay:
98%
Form:
liquid
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InChI key

LPEKGGXMPWTOCB-VKHMYHEASA-N

InChI

1S/C4H8O3/c1-3(5)4(6)7-2/h3,5H,1-2H3/t3-/m0/s1

SMILES string

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

assay

98%

form

liquid

optical activity

[α]18/D −8.1°, neat

optical purity

ee: 97% (GLC)

greener alternative product characteristics

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refractive index

n20/D 1.413 (lit.)

bp

144-145 °C (lit.)

density

1.09 g/mL at 25 °C (lit.)

functional group

ester, hydroxyl

greener alternative category

Quality Level

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General description

(-)-L-乳酸甲酯可用作合成包公藤甲素(一种抗青光眼化合物)的手性助剂。
我们致力于为您带来更环保的替代产品,以符合一项或多项绿色化学12项原则。本化合物性质温和,具有生物降解性和水溶性。可作为制备醋酸纤维素(CA)膜的多功能试剂。也可用作多种化合物、聚合物和衍生物生产的中间体。本品已增强为“更安全的溶剂和助剂”。点击此处了解更多信息。

pictograms

FlameExclamation mark

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Flam. Liq. 3 - STOT SE 3

target_organs

Respiratory system

存储类别

3 - Flammable liquids

wgk

WGK 1

flash_point_f

120.2 °F - closed cup

flash_point_c

49 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

法规信息

危险化学品
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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Methyl (S)-lactate as a chiral auxiliary in the asymmetric synthesis of Bao Gong Teng A.
Pham VC and Charlton JL.
The Journal of Organic Chemistry, 60(24), 8051-8055 (1995)
Chirality-induced switch in hydrogen-bond topology: tetrameric methyl lactate clusters in the gas phase.
Thomas B Adler et al.
Angewandte Chemie (International ed. in English), 45(21), 3440-3445 (2006-05-04)
Nicole Borho et al.
Physical chemistry chemical physics : PCCP, 9(11), 1324-1328 (2007-03-10)
High resolution spectrum of methyl lactate, a chiral alpha-hydroxyester, has been investigated using a molecular jet Fourier transform microwave spectrometer. High level ab initio calculations were employed to study the conformational isomerism of methyl lactate. The observed rotational spectrum confirms
Nicole Borho et al.
Organic & biomolecular chemistry, 1(23), 4351-4358 (2003-12-20)
Chiral recognition and subsequent selective self-organisation into hydrogen-bonded n-mers is observed in supersonic methyl lactate expansions. The nu(OH) and nu(C=O)-vibrations are investigated by ragout-jet FTIR-spectroscopy and lead to the assignment of homo- and heterochiral clusters of at least three different
Jun-Ho Choi et al.
The Journal of chemical physics, 132(7), 074506-074506 (2010-02-23)
Determining absolute configuration of chiral molecule can be achieved by using vibrational optical activity (VOA) measurement methods, such as vibrational circular dichroism and Raman optical activity (ROA). Recently, vibrationally resonant sum frequency generation and difference frequency generation utilizing circularly polarized

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