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Merck
CN

530190

S-Phenyl-L-cysteine

97%

Synonym(s):

3-(Phenylthio)-L-Alanine, 4-Thia-L-homophenylalanine

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About This Item

Linear Formula:
C6H5SCH2CH(NH2)CO2H
CAS Number:
Molecular Weight:
197.25
UNSPSC Code:
12352209
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
2268203
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Quality Level

assay

97%

optical activity

[α]20/D +10°, c = 1.5 in 1 M NaOH

reaction suitability

reaction type: solution phase peptide synthesis

mp

200 °C (dec.) (lit.)

application(s)

peptide synthesis

SMILES string

N[C@@H](CSc1ccccc1)C(O)=O

InChI

1S/C9H11NO2S/c10-8(9(11)12)6-13-7-4-2-1-3-5-7/h1-5,8H,6,10H2,(H,11,12)/t8-/m0/s1

InChI key

XYUBQWNJDIAEES-QMMMGPOBSA-N



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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W E Bechtold et al.
Environmental health perspectives, 104 Suppl 6, 1147-1149 (1996-12-01)
Biological markers of internal dose are useful for improving the extrapolation of health effects from exposures to high levels of toxic air pollutants in animals to low, ambient exposures in humans. Previous results from our laboratory have shown that benzene
W E Bechtold et al.
Carcinogenesis, 13(7), 1217-1220 (1992-07-01)
Results of experiments in our laboratory have shown that benzene is metabolized by animals in part to an intermediate that binds to cysteine groups in hemoglobin to form the adduct S-phenylcysteine (SPC). These results suggested that SPC in hemoglobin may
A A Melikian et al.
Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology, 1(4), 307-313 (1992-05-01)
The present study was aimed at the characterization of the major adducts formed by reaction of the metabolites of [14C]benzene with rat hemoglobin in vivo. Groups of 12-week-old male Fisher rats received i.p. injections of a single dose of 10



Global Trade Item Number

SKUGTIN
530190-5G04061832558479