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P35200

Phenylsuccinic acid

Name: Phenylsuccinic acid
Brand: ALDRICH

98%

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Synonym(s):

(±)-Phenylsuccinic acid

Linear Formula:

HO₂CCH₂CH(C₆H₅)CO₂H

CAS Number:

635-51-8

Molecular Weight:

194.18

Beilstein:

1875051

EC Number:

211-238-1

MDL number:

MFCD00004256

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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Related Categories

Organic Building Blocks

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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The influence of the molecular system on the performance of heteronuclear decoupling in solid-state NMR.

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

Evidence that aspartate aminotransferase activity and ketodicarboxylate carrier function are essential for biosynthesis of transmitter glutamate.

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

The uptake of oxalate by rat liver and kidney mitochondria.

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

Enantioseparation of phenylsuccinic acid by high speed counter-current chromatography using hydroxypropyl-β-cyclodextrin as chiral selector.

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

Role of aspartate aminotransferase and mitochondrial dicarboxylate transport for release of endogenously and exogenously supplied neurotransmitter in glutamatergic neurons.

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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