376906
D-(+)-3-Phenyllactic acid
98%
Synonym(s):
(R)-2-Hydroxy-3-phenylpropionic acid, (R)-3-Phenyllactic acid
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About This Item
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Quality Level
Assay
98%
form
solid
optical activity
[α]20/D +19°, c = 1 in ethanol
mp
122-124 °C (lit.)
functional group
carboxylic acid
hydroxyl
phenyl
SMILES string
O[C@H](Cc1ccccc1)C(O)=O
InChI
1S/C9H10O3/c10-8(9(11)12)6-7-4-2-1-3-5-7/h1-5,8,10H,6H2,(H,11,12)/t8-/m1/s1
InChI key
VOXXWSYKYCBWHO-MRVPVSSYSA-N
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Application
Chiral building block employed in the preparation of statine. Starting material in the preparation of the hypoglycemic agent enlitazone and of 15N-labeled phenylalanine.
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Journal of Heterocyclic Chemistry, 29, 431-431 (1991)
Journal of the Chemical Society. Perkin Transactions 1, 11-11 (1993)
Journal of Heterocyclic Chemistry, 29, 431-431 (1992)
FEMS microbiology letters, 271(2), 310-315 (2007-04-26)
Antifungal compounds from cultures of five type strains of dairy propionibacteria, as well as from the cultivation medium, were studied. Cell-free supernatants and medium were fractionated by C(18) solid phase extraction. The aqueous 95% acetonitrile fractions were analyzed by GC-MS
Se pu = Chinese journal of chromatography, 22(3), 281-283 (2005-02-17)
Various factors affecting the chiral resolution of 3-phenyllactic acid by capillary zone electrophoresis such as the type of cyclodextrin, concentration of the chiral selector, buffer pH, voltage, and temperature were studied and optimized. Using 30 mmol/L hydroxypropyl-beta-cyclodextrin as the chiral
Chromatograms
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