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Documentos Principais

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00160

Sigma-Aldrich

Acetamide

≥99.0% (GC)

Sinônimo(s):

Amide C2

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About This Item

Fórmula linear:
CH3CONH2
Número CAS:
60-35-5
Peso molecular:
59.07
Beilstein:
1071207
Número CE:
200-473-5
Número MDL:
MFCD00008023
Código UNSPSC:
12352111
eCl@ss:
39031237
ID de substância PubChem:
329747009
NACRES:
NA.77

pressão de vapor

1 mmHg ( 65 °C)

Nível de qualidade

200

Ensaio

≥99.0% (GC)

Formulário

crystals

p.e.

221 °C (lit.)

pf

78-80 °C (lit.)
78-82 °C

solubilidade

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

cadeia de caracteres SMILES

CC(N)=O

InChI

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

chave InChI

DLFVBJFMPXGRIB-UHFFFAOYSA-N

Informações sobre genes

rat ... Ggt1(116568)

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Aplicação

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.

Pictogramas

Health hazard
GHS08

Palavra indicadora

Warning

Frases de perigo

H351

Classificações de perigo

Carc. 2

Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 1

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable

Equipamento de proteção individual

dust mask type N95 (US), Eyeshields, Gloves

Escolha uma das versões mais recentes:

Certificados de análise (COA)

Lot/Batch Number
BCCF9094
BCCF1996
BCCB5834
BCBZ9095
BCBW6652

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Pesquise por COA

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Succinamide 98%

Sigma-Aldrich

124753

Succinamide

Isovaleraldehyde 97%

Sigma-Aldrich

146455

Isovaleraldehyde

terc-Butanol analytical standard

Supelco

50621

terc-Butanol

Benzamide 99%

Sigma-Aldrich

135828

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Cesium bromide 99.999% trace metals basis

Sigma-Aldrich

203017

Cesium bromide

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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