P35200
Phenylsuccinic acid
98%
Synonym(s):
(±)-Phenylsuccinic acid
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About This Item
Linear Formula:
HO2CCH2CH(C6H5)CO2H
CAS Number:
Molecular Weight:
194.18
Beilstein:
1875051
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Quality Level
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
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G N Kumar et al.
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Biochemical and biophysical research communications, 202(1), 58-64 (1994-07-15)
Hydroxyproline uptake by rat kidney mitochondria is here first shown by monitoring the reduction of the intramitochondrial pyridine nucleotides which occurs as a result of metabolism of imported hydroxyproline via hydroxyproline oxidase and 3-hydroxy-pyrroline-5-carboxylate dehydrogenase. Widely used criteria for demonstrating
Toru Matsui et al.
Chemosphere, 76(9), 1278-1282 (2009-07-08)
Racemic phenylsuccinate was stereospecifically degraded by the actinomycetes PS9 and PS17 isolated from soil obtained from Okinawa Island, Japan. Strain PS9, identified as a Citricoccus sp., preferentially degraded the R-form, while strain PS17, identified as a Microbacterium sp., preferentially degraded
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
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
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