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B19800

Sigma-Aldrich

S-Benzyl-L-cysteine

97%

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About This Item

Linear Formula:
C6H5CH2SCH2CH(NH2)CO2H
CAS Number:
Molecular Weight:
211.28
Beilstein:
1879358
EC Number:
MDL number:
UNSPSC Code:
12352209
eCl@ss:
32160406
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

97%

form

powder

optical activity

[α]20/D +23°, c = 2 in 1 M NaOH

reaction suitability

reaction type: solution phase peptide synthesis

color

white to off-white

mp

214 °C (dec.) (lit.)

application(s)

detection
peptide synthesis

SMILES string

N[C@@H](CSCc1ccccc1)C(O)=O

InChI

1S/C10H13NO2S/c11-9(10(12)13)7-14-6-8-4-2-1-3-5-8/h1-5,9H,6-7,11H2,(H,12,13)/t9-/m0/s1

InChI key

GHBAYRBVXCRIHT-VIFPVBQESA-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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Mercapturic acid formation in cultured opossum kidney cells.
N Golenhofen et al.
Toxicology letters, 53(1-2), 261-261 (1990-09-01)
B E Hall et al.
Xenobiotica; the fate of foreign compounds in biological systems, 16(7), 609-614 (1986-07-01)
Benzylmercapturic acid is a major metabolite of [methylene-14C]benzyl chloride in the marmoset, as in the rat. The excretion of the minor metabolites benzylmercapturic acid sulphoxide and benzylcysteine accounted for a greater proportion of the dose than in the rat. Excretion
A E Pegg et al.
Biochemistry, 32(45), 11998-12006 (1993-11-16)
Human O6-alkylguanine-DNA alkyltransferase was rapidly inactivated by low concentrations of O6-benzylguanine, but the alkyltransferase from the Escherichia coli ogt gene was much less sensitive and alkyltransferases from the E. coli ada gene or from yeast were not affected. O6-Benzyl-2'-deoxyguanosine was
A Heuner et al.
Pflugers Archiv : European journal of physiology, 417(5), 523-527 (1991-01-01)
We investigated the capacity and the localization of N-acetylation of the mercapturic acid precursor S-benzyl-L-cysteine (BC), as well as the tubular reabsorption of this compound in the rat kidney in vivo et situ by renal clearance and continuous microinfusion and

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