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About This Item
Linear Formula:
C6H5CH(OH)CO2H
CAS Number:
Molecular Weight:
152.15
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
202-007-6
MDL number:
Assay:
99%
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
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.
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signalword
Danger
hcodes
Hazard Classifications
Eye Dam. 1
Storage Class
13 - Non Combustible Solids
wgk
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)
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.
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.
Global Trade Item Number
| SKU | GTIN |
|---|---|
| M2101-250G | 04061834041580 |
| M2101-500G | 04061834041597 |
