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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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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
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
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
G K Asimakis et al.
The American journal of physiology, 249(5 Pt 2), H1009-H1016 (1985-11-01)
Adenine nucleotide efflux from isolated rat heart mitochondria was studied. Inorganic phosphate induced efflux of adenine nucleotides from the mitochondria. This efflux was inhibited by carboxyatractyloside and atractyloside. The rate of efflux showed saturation kinetics with respect to extramitochondrial phosphate
D E Wilson et al.
Biochimica et biophysica acta, 893(3), 470-479 (1987-10-07)
Upon the addition of inorganic phosphate, isolated rat-heart mitochondria released endogenous adenine nucleotides. To elucidate the mechanism of this phosphate-induced efflux, we evaluated the relative roles of three inner mitochondrial membrane carriers: the adenine nucleotide translocase, the phosphate/hydroxyl exchanger, and
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