(S)-(+)-mandelic acid
benzeneacetic acid, a-hydroxy-, (S)-
Identification
| Name | (S)-(+)-mandelic acid |
| CAS Number | 17199-29-0 |
| EINECS | 241-240-8 |
| FDA UNII | L0UMW58G3T |
| Molecular Formula | C8 H8 O3 |
| Molecular Weight | 152.14936000 |
| MDL Number | MFCD00004495 |
| Nikkaji Number | J74.069A |
| Beilstein | 2208678 |
| XlogP3 | 0.60 (est) |
Regulatory
Physical Properties
| Assay | 95.00 to 100.00 |
| Food Chemicals Codex Listed | No |
| Melting Point | 134.00 °C. @ 760.00 mm Hg |
| Boiling Point | 321.83 °C. @ 760.00 mm Hg (est) |
| Flash Point | 325.00 °F. TCC ( 162.60 °C. ) (est) |
| logP (o/w) | 0.550 (est) |
| Soluble in | water, 2.20E+05 mg/L @ 25 °C (exp) |
No sensory data available
Safety Information
| Preferred SDS | View |
| Oral/Parenteral Toxicity | Not determined |
| Dermal Toxicity | Not determined |
| Inhalation Toxicity | Not determined |
GHS Classification
['GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)', 'GHS Label elements, including precautionary statements']
Safety in Use
| Category | pharmaceuticals / chemical synthisis |
| Recommendation for (S)-(+)-mandelic acid usage levels up to | not for fragrance use. |
| Recommendation for (S)-(+)-mandelic acid flavor usage levels up to | not for flavor use. |
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Potential Uses
Natural Occurrence
Synonyms
benzeneacetic acid, a-hydroxy-, (aS)-
benzeneacetic acid, a-hydroxy-, (S)-
(2S)-2-
hydroxy-2-phenylacetic acid
(S)-(+)-2-
hydroxy-2-phenylacetic acid
(S)-2-
hydroxy-2-phenylacetic acid
(S)-
hydroxy-phenyl-acetic acid
(2S)-
hydroxy(phenyl)acetic acid
(2S)-
hydroxy(phenyl)ethanoic acid
(S)-a-
hydroxybenzeneacetic acid
(S)-(+)-a-
hydroxyphenylacetic acid
(S)-a-
hydroxyphenylacetic acid
(+)-
mandelic acid
(+)-(S)-
mandelic acid
(S)-
mandelic acid
L-
mandelic acid
L-(+)-
mandelic acid
S-
mandelic acid
S-(+)-
mandelic acid
S(+)-
mandelic acid
(S)-(+)-
mandelicacid
PubMed:
Alditols and monosaccharides from sorghum vinegar can attenuate platelet aggregation by inhibiting cyclooxygenase-1 and thromboxane-A2 synthase.
PubMed:
Improvement of Alcaligenes faecalis nitrilase by gene site saturation mutagenesis and its application in stereospecific biosynthesis of (R)-(-)-mandelic acid.
PubMed:
Derivation of safe health-based exposure limits for potential consumer exposure to styrene migrating into food from food containers.
PubMed:
Oxidative decarboxylation of mandelic acid derivative by recombinant Escherichia coli: a novel method of ethyl vanillin synthesis.
PubMed:
Gene cloning, expression, and characterization of a nitrilase from Alcaligenes faecalis ZJUTB10.
PubMed:
Determination of mandelic acid enantiomers in urine by derivatization in supercritical carbon dioxide prior to their determination by gas chromatography.
PubMed:
Hydrolysis of nitriles using an immobilized nitrilase: applications to the synthesis of methionine hydroxy analogue derivatives.
PubMed:
Construction of an electro-enzymatic bioreactor for the production of (R)-mandelate from benzoylformate.
PubMed:
Clinical efficacy of a chlorous acid preoperative skin antiseptic.
PubMed:
Broiler skin color as affected by organic acids: influence of concentration and method of application.