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(S)-(+)-mandelic acid
benzeneacetic acid, a-hydroxy-, (S)-

Supplier Sponsors

CAS Number: 17199-29-0Picture of molecule3D/inchi
Other(deleted CASRN):14447-36-0
ECHA EINECS - REACH Pre-Reg:241-240-8
FDA UNII: L0UMW58G3T
Nikkaji Web:J74.069A
Beilstein Number:2208678
MDL:MFCD00004495
XlogP3:0.60 (est)
Molecular Weight:152.14936000
Formula:C8 H8 O3
BioActivity Summary:listing
NMR Predictor:Predict (works with chrome, Edge or firefox)
Category:pharmaceuticals / chemical synthisis
 
US / EU / FDA / JECFA / FEMA / FLAVIS / Scholar / Patent Information:
Google Scholar:Search
Google Books:Search
Google Scholar: with word "volatile"Search
Google Scholar: with word "flavor"Search
Google Scholar: with word "odor"Search
Google Patents:Search
US Patents:Search
EU Patents:Search
Pubchem Patents:Search
PubMed:Search
NCBI:Search
 
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)
 water, 1.763e+005 mg/L @ 25 °C (est)
 
Organoleptic Properties:
Odor and/or flavor descriptions from others (if found).
 
Cosmetic Information:
None found
 
Suppliers:
BOC Sciences
For experimental / research use only.
(S)-Hydroxy-phenyl-acetic acid 98%
Changzhou Longo Chemical
(S)-(+)-Mandelic Acid
Glentham Life Sciences
L-(+)-Mandelic acid
Santa Cruz Biotechnology
For experimental / research use only.
(S)-(+)-Mandelic Acid
Sigma-Aldrich: Aldrich
For experimental / research use only.
(S)-(+)-Mandelic Acid ReagentPlus®, ≥99%
sds
TCI AMERICA
For experimental / research use only.
L-(+)-Mandelic Acid >99.0%(GC)(T)
sds
 
Safety Information:
Preferred SDS: View
 
Hazards identification
 
Classification of the substance or mixture
GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)
None found.
GHS Label elements, including precautionary statements
 
Pictogram
 
Hazard statement(s)
None found.
Precautionary statement(s)
None found.
Oral/Parenteral Toxicity:
Not determined
Dermal Toxicity:
Not determined
Inhalation Toxicity:
Not determined
 
Safety in Use Information:
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.
 
Safety References:
EPI System: View
AIDS Citations:Search
Cancer Citations:Search
Toxicology Citations:Search
EPA Substance Registry Services (TSCA):17199-29-0
EPA ACToR:Toxicology Data
EPA Substance Registry Services (SRS):Registry
Laboratory Chemical Safety Summary :439616
National Institute of Allergy and Infectious Diseases:Data
WGK Germany:3
(2S)-2-hydroxy-2-phenylacetic acid
Chemidplus:0017199290
 
References:
 (2S)-2-hydroxy-2-phenylacetic acid
NIST Chemistry WebBook:Search Inchi
Canada Domestic Sub. List:17199-29-0
Pubchem (cid):439616
Pubchem (sid):135043471
 
Other Information:
(IUPAC):Atomic Weights of the Elements 2011 (pdf)
Videos:The Periodic Table of Videos
tgsc:Atomic Weights use for this web site
(IUPAC):Periodic Table of the Elements
CHEBI:View
CHEMBL:View
UM BBD:Search
KEGG (GenomeNet):C01984
HMDB (The Human Metabolome Database):HMDB00703
Export Tariff Code:2918.19.1200
ChemSpider:View
Wikipedia:View
 
Potential Blenders and core components note
None Found
 
Potential Uses:
None Found
 
Occurrence (nature, food, other):note
 not found in nature
 
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
 

Articles:

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.
 
Notes:
None found
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