M2101
Mandelic acid
99%
Synonym(s):
(RS)-Mandelic acid, (±)-Mandelic Acid, DL-Mandelic acid, Racemic mandelic acid
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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)
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
G L Corona et al.
European archives of psychiatry and neurological sciences, 239(2), 79-86 (1989-01-01)
Memory performance, central monoaminergic function and sympathetic nerve activity were studied in patients with dementia of the Alzheimer type (DAT) or with multi-infarct dementia before and after 4 weeks with single or combined drug therapy (choline-piracetam). Analysis of the levels
Global Trade Item Number
| SKU | GTIN |
|---|---|
| M2101-250G | 04061834041580 |
| M2101-500G | 04061834041597 |