V000908
DL-Mandelic acid
99%
Synonym(s):
(±)-α-Hydroxyphenylacetic acid
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About This Item
Linear Formula:
C6H5CH(OH)COOH
CAS Number:
Molecular Weight:
152.15
Beilstein:
510011
EC Number:
MDL number:
PubChem Substance ID:
Assay
99%
SMILES string
OC(C(O)=O)c1ccccc1
InChI
1S/C8H8O3/c9-7(8(10)11)6-4-2-1-3-5-6/h1-5,7,9H,(H,10,11)
InChI key
IWYDHOAUDWTVEP-UHFFFAOYSA-N
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Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Dam. 1
Storage Class Code
13 - Non Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Regulatory Information
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[Mandelic acid in urine].
Hideki Igisu et al.
Nihon rinsho. Japanese journal of clinical medicine, 62 Suppl 12, 482-484 (2005-01-22)
[Mandelic acid in urine].
H Igisu et al.
Nihon rinsho. Japanese journal of clinical medicine, 57 Suppl, 454-456 (1999-09-30)
Huihui Sun et al.
Biotechnology letters, 37(8), 1655-1661 (2015-04-10)
To examine nitrilase-mediated hydrolysis of nitriles to produce optically pure α-hydroxycarboxylic acids. A novel nitrilase, GPnor51, from Luminiphilus syltensis NOR5-1B was discovered by genomic data mining. It could hydrolyze racemic o-chloromandelonitrile to (R)-o-chloromandelic acid with high enantioselectivity (ee 98.2 %).
Hualei Wang et al.
Applied and environmental microbiology, 81(24), 8469-8477 (2015-10-04)
The nitrilase-mediated pathway has significant advantages in the production of optically pure aromatic α-hydroxy carboxylic acids. However, low enantioselectivity and activity are observed on hydrolyzing o-chloromandelonitrile to produce optically pure (R)-o-chloromandelic acid. In the present study, a protein engineering approach
Dima Albals et al.
Electrophoresis, 35(19), 2807-2818 (2014-07-02)
A generic chiral separation strategy for the analysis of acidic compounds in CEC is proposed in completion of an earlier defined strategy for nonacidic compounds. The screening step of this strategy uses a 45 mM ammonium formate (pH 2.9)/ACN (35/65
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