67787
N-(Methyl)mercaptoacetamide
≥97.0% (RT)
Synonym(s):
N-(Methyl)thioglycolamide
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About This Item
Linear Formula:
HSCH2CONHCH3
CAS Number:
Molecular Weight:
105.16
UNSPSC Code:
12352200
NACRES:
NA.25
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
1740652
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InChI
1S/C3H7NOS/c1-4-3(5)2-6/h6H,2H2,1H3,(H,4,5)
SMILES string
CNC(=O)CS
InChI key
NSJNRJYQQPRCLF-UHFFFAOYSA-N
assay
≥97.0% (RT)
refractive index
n20/D 1.523
bp
83-85 °C/0.3 mmHg
density
1.19 g/mL at 20 °C (lit.)
storage temp.
2-8°C
Application
N-(Methyl)mercaptoacetamide is a reducing agent that reacts with methionine sulfoxide moieties. N-(Methyl)mercaptoacetamide may be used as a reference material in assays wherein this molecule is an expected leaving group. N-(Methyl)mercaptoacetamide is used in various zinc complexes to study metalloprotein structure and interactions.
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David T Puerta et al.
Inorganic chemistry, 41(20), 5075-5082 (2002-10-02)
The tetrahedral zinc complex [(Tp(Me,Ph))ZnOH] (Tp(Me,Ph) = hydrotris(5,3-methylphenylpyrazolyl)borate) was combined with acetohydroxamic acid, 3-mercapto-2-butanone, N-(methyl)mercaptoacetamide, beta-mercaptoethanol, 3-mercapto-2-propanol, and 3-mercapto-2-butanol to generate the complexes [(Tp(Me,Ph))Zn(ZBG)] (ZBG = zinc-binding group). These complexes were prepared to determine the mode of binding for three
R.I. Lundblad et al.
Chemical Reagents for Protein Modification, I, 99-99 (1984)
Isolation and biochemical characterization of a novel lantibiotic mutacin from Streptococcus mutans.
J Novák et al.
Journal of bacteriology, 176(14), 4316-4320 (1994-07-01)
Certain members of the indigenous biota of humans produce antimicrobial substances called bacteriocins, which inhibit other bacteria, including members of their own species. One of these substances, mutacin, is made by Streptococcus mutans, a member of the oral biota. Mutacin
Peter Eyer et al.
Biochemical pharmacology, 75(10), 2045-2053 (2008-04-04)
Isodimethoate is a thermal decomposition product that is present in usual pesticide formulations of dimethoate. Owing to its PO structure the compound is a direct anticholinesterase agent whose properties, to the best of our knowledge, are presented here for the
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