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P35200

Sigma-Aldrich

Phenylsuccinic acid

98%

Sinonimo/i:

(±)-Phenylsuccinic acid

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About This Item

Formula condensata:
HO2CCH2CH(C6H5)CO2H
Numero CAS:
635-51-8
Peso molecolare:
194.18
Beilstein:
1875051
Numero CE:
211-238-1
Numero MDL:
MFCD00004256
Codice UNSPSC:
12352100
ID PubChem:
24898421
NACRES:
NA.22

Saggio

98%

Forma fisica

powder

Punto di fusione

166-168 °C (lit.)

Stringa SMILE

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)
LVFFZQQWIZURIO-UHFFFAOYSA-N

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Categorie correlate

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

Eyeshields, Gloves, type N95 (US)

Certificati d'analisi (COA)

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2-Propanolo anhydrous, 99.5%

Sigma-Aldrich

278475

2-Propanolo

G N Kumar et al.
Current eye research, 12(6), 501-506 (1993-06-01)
Soft drug analogs of methscopolamine (4 a-c) were tested for mydriatic activity in rabbits' eyes. After unilateral administration of equieffective doses, the AUC24hrs and the mydriatic recovery times were found to be significantly lower with the soft drugs compared to
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
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
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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