Skip to Content
Merck
All Photos(1)

Key Documents

A0500

Sigma-Aldrich

Acetamide

~99% (GC)

Synonym(s):

Amide C2

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
CH3CONH2
CAS Number:
Molecular Weight:
59.07
Beilstein:
1071207
EC Number:
MDL number:
UNSPSC Code:
12352111
PubChem Substance ID:
NACRES:
NA.77

biological source

synthetic

Quality Level

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

SMILES string

CC(N)=O

InChI

1S/C2H5NO/c1-2(3)4/h1H3,(H2,3,4)

InChI key

DLFVBJFMPXGRIB-UHFFFAOYSA-N

Gene Information

Looking for similar products? Visit Product Comparison Guide

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

Pictograms

Health hazard

Signal Word

Warning

Hazard Statements

Hazard Classifications

Carc. 2

Storage Class Code

11 - Combustible Solids

WGK

WGK 1

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Already Own This Product?

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

Visit the Document Library

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)
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)
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)
Muscle Satellite Cell Cross-Talk with a Vascular Niche Maintains Quiescence via VEGF and Notch Signaling
Verma M, et al.
Cell Stem Cell, 23(4), 530-543 (2018)
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

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