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Key Documents

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00160

Sigma-Aldrich

Acetamide

≥99.0% (GC)

Sinónimos:

Amide C2

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About This Item

Fórmula lineal:
CH3CONH2
Número de CAS:
60-35-5
Peso molecular:
59.07
Beilstein/REAXYS Number:
1071207
EC Number:
200-473-5
MDL number:
MFCD00008023
UNSPSC Code:
12352111
eCl@ss:
39031237
PubChem Substance ID:
329747009
NACRES:
NA.77

vapor pressure

1 mmHg ( 65 °C)

Quality Level

200

assay

≥99.0% (GC)

form

crystals

bp

221 °C (lit.)

mp

78-80 °C (lit.)
78-82 °C

solubility

H2O: soluble 1 gm in 0.5 ml
alcohol: soluble 1 gm in 2ml
pyridine: soluble 1 gm in 6 ml
chloroform: soluble
glycerol: soluble

SMILES string

CC(N)=O

InChI

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

InChI key

DLFVBJFMPXGRIB-UHFFFAOYSA-N

Gene Information

rat ... Ggt1(116568)

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Application

Acetamide was used as a supplement for growth media and for complementation of tlyA transposon mutants.The product was used as a component for cryoprotectant solution to study the ultrastructural changes in bovine oocytes by using vitrification.

pictograms

Health hazard
GHS08

signalword

Warning

hcodes

H351

Hazard Classifications

Carc. 2

Storage Class

11 - Combustible Solids

wgk_germany

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificados de análisis (COA)

Lot/Batch Number
BCCF9094
BCCF1996
BCCB5834
BCBZ9095
BCBW6652

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E Fuku et al.
Cryobiology, 32(2), 139-156 (1995-04-01)
Oocytes recovered from abattoir-derived ovaries were exposed to a cryoprotectant solution (DAP213: 2 M DMSO, 1 M acetamide, 3 M propanediol, and 10% fetal calf serum in tissue culture medium 199) for less than 20 s and vitrified either at
Courtney E Maus et al.
Antimicrobial agents and chemotherapy, 49(2), 571-577 (2005-01-28)
Capreomycin, an important drug for the treatment of multidrug-resistant tuberculosis, is a macrocyclic peptide antibiotic produced by Saccharothrix mutabolis subspecies capreolus. The basis of resistance to this drug was investigated by isolating and characterizing capreomycin-resistant strains of Mycobacterium smegmatis and
Lingle Wang et al.
Proceedings of the National Academy of Sciences of the United States of America, 109(6), 1937-1942 (2012-02-07)
We apply a free energy perturbation simulation method, free energy perturbation/replica exchange with solute tempering, to two modifications of protein-ligand complexes that lead to significant conformational changes, the first in the protein and the second in the ligand. The approach
Jie Guang et al.
Organic letters, 14(12), 3174-3177 (2012-06-02)
Highly enantioselective aldol reactions of acetylphosphonates and activated carbonyl compounds was realized with cinchona alkaloid derived catalysts, in which the acetylphosphonate was directly used as an enolate precursor for the first time. The aldol product obtained was converted in situ
Cristian Varela et al.
Chemistry & biology, 19(4), 498-506 (2012-04-24)
Mycolic acids are vital components of the cell wall of the tubercle bacillus Mycobacterium tuberculosis and are required for viability and virulence. While mycolic acid biosynthesis is studied extensively, components involved in mycolate transport remain unidentified. We investigated the role
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