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P35200

Sigma-Aldrich

Phenylsuccinic acid

98%

Sinónimos:

(±)-Phenylsuccinic acid

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About This Item

Fórmula lineal:
HO2CCH2CH(C6H5)CO2H
Número de CAS:
635-51-8
Peso molecular:
194.18
Beilstein/REAXYS Number:
1875051
EC Number:
211-238-1
MDL number:
MFCD00004256
UNSPSC Code:
12352100
PubChem Substance ID:
24898421
NACRES:
NA.22

Quality Level

200

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

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

Certificados de análisis (COA)

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Sigma-Aldrich

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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
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
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
A Atlante et al.
Biochemical and biophysical research communications, 132(1), 8-18 (1985-10-15)
Fumarate permeation in isolated rat liver mitochondria was demonstrated by measuring malate and phosphate efflux caused by fumarate added externally to the mitochondrial suspension. The existence of two specific fumarate translocators, fumarate/malate and fumarate/phosphate, is shown here. These carriers are
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