S-Phenyl-L-cysteine

Modify Date: 2024-01-04 16:00:03

S-Phenyl-L-cysteine Structure
S-Phenyl-L-cysteine structure
Common Name S-Phenyl-L-cysteine
CAS Number 34317-61-8 Molecular Weight 197.25
Density 1.3±0.1 g/cm3 Boiling Point 361.5±37.0 °C at 760 mmHg
Molecular Formula C9H11NO2S Melting Point 200 °C (dec.)(lit.)
MSDS Chinese USA Flash Point 172.4±26.5 °C

 Use of S-Phenyl-L-cysteine


S-Phenylcysteine is acysteine derivatives.

 Names

Name (2R)-2-amino-3-phenylsulfanylpropanoic acid
Synonym More Synonyms

 S-Phenyl-L-cysteine Biological Activity

Description S-Phenylcysteine is acysteine derivatives.
Related Catalog

 Chemical & Physical Properties

Density 1.3±0.1 g/cm3
Boiling Point 361.5±37.0 °C at 760 mmHg
Melting Point 200 °C (dec.)(lit.)
Molecular Formula C9H11NO2S
Molecular Weight 197.25
Flash Point 172.4±26.5 °C
Exact Mass 197.051056
PSA 88.62000
LogP 1.86
Vapour Pressure 0.0±0.9 mmHg at 25°C
Index of Refraction 1.624

 Safety Information

Personal Protective Equipment Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
Hazard Codes Xi:Irritant;
Risk Phrases R36/37/38
Safety Phrases S37/39-S26
RIDADR NONH for all modes of transport
WGK Germany 3
HS Code 2930909090

 Synthetic Route

 Customs

HS Code 2930909090
Summary 2930909090. other organo-sulphur compounds. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

 Articles8

More Articles
Comparative study on the bioactivation mechanisms and cytotoxicity of Te-phenyl-L-tellurocysteine, Se-phenyl-L-selenocysteine, and S-phenyl-L-cysteine.

Chem. Res. Toxicol. 15(12) , 1610-8, (2002)

Tellurium compounds are effective antioxidants and chemoprotectors, even more active than their selenium and sulfur analogues. In addition to these properties, some selenium compounds, such as selenoc...

Biomarkers of human exposure to benzene.

J. Toxicol. Environ. Health A 40(2-3) , 377-86, (1993)

Three biomarkers for benzene exposure were developed. The first biomarker, muconic acid in urine, results from the ring opening of a benzene metabolite. A gas chromatography/mass spectroscopy (GC/MS) ...

S-phenylcysteine formation in hemoglobin as a biological exposure index to benzene.

Arch. Toxicol. 66(5) , 303-9, (1992)

Benzene is metabolized to intermediates that bind to hemoglobin, forming adducts. These hemoglobin adducts may be usable as biomarkers of exposure. In this paper, we describe the development of a gas ...

 Synonyms

MFCD01318758
(2R)-2-amino-3-phenylthiopropanoic acid
S-phenyl-L-cysteine
L-Cysteine,S-phenyl
(L)-2-amino-3-(phenylthio)propanoic acid
(R)-S-Phenylcystein
Cysteine, S-phenyl-
S-Phenylcysteine
3-(Phenylthio)-L-Alanine,4-Thia-L-homophenylalanine
QVYZ1SR &&L or R Form
4-Thia-L-homophenylalanine
3-Phenylcysteine
L-S-phenylcysteine
(R)-S-phenylcysteine
S-Ph-L-cysteine
(R)-2-Amino-3-(phenylthio)propanoic acid
3-(Phenylthio)-L-Alanine
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