Skip to Content
Merck
All Photos(1)

Documents

B5890

Sigma-Aldrich

S-tert-Butylmercapto-L-cysteine

Synonym(s):

3-(tert-Butyldithio)-L-alanine, S-(tert-Butylthio)-L-cysteine

Sign Into View Organizational & Contract Pricing


About This Item

Empirical Formula (Hill Notation):
C7H15NO2S2
CAS Number:
Molecular Weight:
209.33
Beilstein:
2247500
EC Number:
MDL number:
UNSPSC Code:
12352209
PubChem Substance ID:
NACRES:
NA.26

form

powder

color

white to faint yellow

application(s)

peptide synthesis

SMILES string

CC(C)(C)SSC[C@H](N)C(O)=O

InChI

1S/C7H15NO2S2/c1-7(2,3)12-11-4-5(8)6(9)10/h5H,4,8H2,1-3H3,(H,9,10)/t5-/m0/s1

InChI key

TWMBHZTWEDJDRC-YFKPBYRVSA-N

Looking for similar products? Visit Product Comparison Guide

Application

S-tert-butylmercapto-L-cysteine may be used to introduce synthetically useful S-tert-butylthio groups into peptides.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable


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’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

E Wünsch et al.
International journal of peptide and protein research, 32(5), 368-383 (1988-11-01)
In human IgGl the two heavy chains are crosslinked in the central portion of the molecule by two disulfide bridges forming a double chain bis-cystinyl cyclic peptide in parallel alignment. For our synthetic studies we have chosen the sequence portion

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service