M2101
Mandelic acid
99%
Synonym(s):
(RS)-Mandelic acid, (±)-Mandelic Acid, DL-Mandelic acid, Racemic mandelic acid
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250 G
$55.90
500 G
$82.70
About This Item
Linear Formula:
C6H5CH(OH)CO2H
CAS Number:
Molecular Weight:
152.15
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
assay:
99%
Recommended Products
Quality Level
assay
99%
mp
119-121 °C (lit.)
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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Application
Racemic mandelic acid in the form of mandelates is generally used as a pharmaceutical component due to its analgesic, antirheumatic, and spasmolytic effects. It undergoes resolution to form (+)- and (-)-enantiomers that are widely used as chiral resolving agents in enantioseparation of various other racemates via salt formation.[1]
signalword
Danger
hcodes
Hazard Classifications
Eye Dam. 1
Storage Class
13 - Non Combustible Solids
wgk_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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Enantiomeric mandelic acid system melting point phase diagram and solubility in water.
Lorenz H, et al.
Journal of Chemical and Engineering Data, 47(5), 1280-1284 (2002)
P Vodicka et al.
Carcinogenesis, 16(7), 1473-1481 (1995-07-01)
Occupational exposure to styrene was studied in nine workers of a hand lamination plant in Bohemia. Personal dosimeters were used to monitor the styrene workplace exposure, and the levels of styrene in blood and mandelic acid in urine were measured.
Ludmila Krivánková et al.
Electrophoresis, 24(3), 505-517 (2003-02-06)
Effects originating from the variability of the sample matrix can be efficiently eliminated when the separation conditions are selected so that compounds of like charge with high concentration referred to as macrocomponents are embodied into the system of transient isotachophoresis.
A Kimura et al.
Pediatric research, 45(4 Pt 1), 603-609 (1999-04-15)
Unusual bile acids, such as unsaturated ketonic and 7beta-hydroxylated bile acids, have been detected in urine early in life. To elucidate the normal profiles of usual and unusual urinary bile acids in the neonatal and pediatric periods, we measured the
David A Ostrov et al.
Antimicrobial agents and chemotherapy, 51(10), 3688-3698 (2007-08-08)
The bacterial type II topoisomerases DNA gyrase and topoisomerase IV are validated targets for clinically useful quinolone antimicrobial drugs. A significant limitation to widely utilized quinolone inhibitors is the emergence of drug-resistant bacteria due to an altered DNA gyrase. To
Chromatograms
suitable for GCsuitable for GCActive Filters
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