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
Beilstein:
1875051
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Quality Level
Assay
98%
form
powder
mp
166-168 °C (lit.)
SMILES string
OC(=O)CC(C(O)=O)c1ccccc1
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
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Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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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
Guillaume Gerbaud et al.
Journal of magnetic resonance (San Diego, Calif. : 1997), 210(1), 75-81 (2011-03-09)
The intensity of the carbon signal in a CPMAS experiment has been measured for two CH and three CH(2) moieties in four test molecules under different phase-modulated proton decoupling conditions and as a function of the spinning rate. The proton
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
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