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P35200

Sigma-Aldrich

Phenylsuccinic acid

98%

Synonym(s):

(±)-Phenylsuccinic acid

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About This Item

Linear Formula:
HO2CCH2CH(C6H5)CO2H
CAS Number:
635-51-8
Molecular Weight:
194.18
Beilstein:
1875051
EC Number:
211-238-1
MDL number:
MFCD00004256
UNSPSC Code:
12352100
PubChem Substance ID:
24898421
NACRES:
NA.22

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

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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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
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
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
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
G Palaiologos et al.
Neurochemical research, 14(4), 359-366 (1989-04-01)
Evoked release of glutamate and aspartate from cultured cerebellar granule cells was studied after preincubation of the cells in tissue culture medium with glucose (6.5 mM), glutamine (1.0 mM), D[3H] aspartate and in some cases aminooxyacetate (5.0 mM) or phenylsuccinate
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