P35200
Phenylsuccinic acid
98%
Synonym(s):
(±)-Phenylsuccinic acid
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About This Item
Linear Formula:
HO2CCH2CH(C6H5)CO2H
CAS Number:
Molecular Weight:
194.18
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
211-238-1
Beilstein/REAXYS Number:
1875051
MDL number:
Assay:
98%
Form:
powder
InChI
1S/C10H10O4/c11-9(12)6-8(10(13)14)7-4-2-1-3-5-7/h1-5,8H,6H2,(H,11,12)(H,13,14)
InChI key
LVFFZQQWIZURIO-UHFFFAOYSA-N
SMILES string
OC(=O)CC(C(O)=O)c1ccccc1
assay
98%
form
powder
Quality Level
Related Categories
Storage Class
11 - 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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G N Kumar et al.
Current eye research, 12(6), 501-506 (1993-06-01)
Soft drug analogs of methscopolamine (4 a-c) were tested for mydriatic activity in rabbits' eyes. After unilateral administration of equieffective doses, the AUC24hrs and the mydriatic recovery times were found to be significantly lower with the soft drugs compared to
Toru Matsui et al.
Chemosphere, 76(9), 1278-1282 (2009-07-08)
Racemic phenylsuccinate was stereospecifically degraded by the actinomycetes PS9 and PS17 isolated from soil obtained from Okinawa Island, Japan. Strain PS9, identified as a Citricoccus sp., preferentially degraded the R-form, while strain PS17, identified as a Microbacterium sp., preferentially degraded
G Palaiologos et al.
Journal of neurochemistry, 51(1), 317-320 (1988-07-01)
Based on the selective inhibition of glutamate release in cerebellar granule cells in primary cultures by the aspartate aminotransferase inhibitor, aminooxyacetic acid, and by the ketodicarboxylate carrier inhibitor, phenylsuccinate, a novel model for synthesis of transmitter glutamate is suggested: Glutamate
Shengqiang Tong et al.
Journal of chromatography. A, 1218(33), 5602-5608 (2011-07-15)
High speed counter-current chromatography (HSCCC) was successfully applied to resolution of phenylsuccinic acid (PSA) with hydroxypropyl-β-cyclodextrin (HP-β-CD) as chiral selector (CS). The two-phase solvent system composed of n-hexane-methyl tert-butyl ether-0.1 mol L⁻¹ phosphate buffer solution with pH=2.51 (0.5:1.5:2, v/v/v) was
T Strzelecki et al.
The Journal of biological chemistry, 261(26), 12197-12201 (1986-09-15)
Oxalate, a metabolic end product, forms calcium oxalate deposits in the tissues under a variety of pathological conditions. In order to determine whether oxalate is able to penetrate the mitochondrial matrix, the uptake of oxalate by rat liver and kidney
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