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P35200

Phenylsuccinic acid

Name: Phenylsuccinic acid
Brand: ALDRICH

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

UNSPSC Code:

12352100

NACRES:

NA.22

PubChem Substance ID:

24898421

EC Number:

211-238-1

Beilstein/REAXYS Number:

1875051

MDL number:

MFCD00004256

Assay:

98%

Form:

powder

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Properties

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

Description

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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Effects of phenylsuccinate on potassium-stimulated taurine release in cultured neurons and astrocytes and in rat hippocampus in vivo.

T Bruhn et al.

Journal of neuroscience research, 46(2), 198-203 (1996-10-15)

Swelling-induced release of taurine was investigated in vivo in hippocampus by microdialysis or in vitro in cultured neocortical neurons or astrocytes. Swelling was induced either by increasing the extracellular K+ concentration or by exposing the cells to hyposmotic conditions. It

Electrochemical β-Selective Hydrocarboxylation of Styrene Using CO2 and Water.

Younghye Kim et al.

Advanced science (Weinheim, Baden-Wurttemberg, Germany), 7(3), 1900137-1900137 (2020-02-12)

The carboxylation of hydrocarbons using CO2 as a one-carbon building block is an attractive route for the synthesis of carboxylic acids and their derivatives. Until now, chemical carboxylation catalyzed by organometallic nucleophiles and reductants has been generally adopted particularly for

Neuroprotective effect of phenylsuccinate, an inhibitor of cytosolic glutamate formation from glutamine, under anoxic conditions but not during exposure to exogenous glutamate.

R Huang et al.

Neuroscience letters, 183(1-2), 22-26 (1995-01-02)

Phenylsuccinate is an inhibitor of cytosolic glutamate formation from extracellular glutamine in cultured cerebellar granule cell neurons, a glutamatergic preparation. It prevents anoxic cell death in these cells as indicated by decreased lactate dehydrogenase (LDH) release and by the morphological

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