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About This Item
Linear Formula:
CH3CONH2
CAS Number:
Molecular Weight:
59.07
UNSPSC Code:
12352111
NACRES:
NA.77
PubChem Substance ID:
EC Number:
200-473-5
Beilstein/REAXYS Number:
1071207
MDL number:
InChI key
DLFVBJFMPXGRIB-UHFFFAOYSA-N
InChI
1S/C2H5NO/c1-2(3)4/h1H3,(H2,3,4)
SMILES string
CC(N)=O
biological source
synthetic
vapor pressure
1 mmHg ( 65 °C)
assay
~99% (GC)
form
powder or crystals
bp
221 °C (lit.)
mp
78-80 °C (lit.)
solubility
water: 0.2 g/L, clear, colorless
Quality Level
Gene Information
rat ... Ggt1(116568)
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General description
Acetamide based derivatives are potential anti-microbial, antifungal agents, used as disinfectants. Cigarette smoking triggers acetamide release. It is a minor by-product of paracetamol degradation. Acetamide is carcinogenic in rats.
Application
Acetamide has been used:
- for the induction of recombinant protein in M. smegmatis
- as a component of acetamide medium for fungal selection
- in quenching experiment in mice tissue samples
signalword
Warning
hcodes
Hazard Classifications
Carc. 2
Storage Class
11 - Combustible Solids
wgk
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type P3 (EN 143) respirator cartridges
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Cell Stem Cell, 23(4), 530-543 (2018)
The RD1 proteins of Mycobacterium tuberculosis: expression in Mycobacterium smegmatis and biochemical characterization
Daugelat S, et al.
Microbes and Infection, 5(12), 1082-1095 (2003)
Gas chromatographic?mass spectrometric analysis of acrylamide and acetamide in cigarette mainstream smoke after on-column injection
Diekmann J, et al.
Journal of Chromatographic Science, 46(7), 659-663 (2008)
Maureen Hamilton et al.
Microbial cell factories, 19(1), 22-22 (2020-02-07)
Yarrowia lipolytica is an oleaginous yeast that can be genetically engineered to produce lipid and non-lipid biochemicals from a variety of feedstocks. Metabolic engineering of this organism usually requires genetic markers in order to select for modified cells. The potential
Synthesis of biologically active 2-chloro-N-alkyl/aryl acetamide derivatives
Katke SA, et al.
International Journal of Pharma Sciences and Research, 2, 148-156 (2011)
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