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00160

Sigma-Aldrich

Acetamide

≥99.0% (GC)

Sinonimo/i:

Amide C2

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About This Item

Formula condensata:
CH3CONH2
Numero CAS:
60-35-5
Peso molecolare:
59.07
Beilstein:
1071207
Numero CE:
200-473-5
Numero MDL:
MFCD00008023
Codice UNSPSC:
12352111
eCl@ss:
39031237
ID PubChem:
329747009
NACRES:
NA.77

Tensione di vapore

1 mmHg ( 65 °C)

Livello qualitativo

200

Saggio

≥99.0% (GC)

Stato

crystals

P. ebollizione

221 °C (lit.)

Punto di fusione

78-80 °C (lit.)
78-82 °C

Solubilità

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

Stringa SMILE

CC(N)=O

InChI

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

Informazioni sul gene

rat ... Ggt1(116568)

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Applicazioni

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.

Pittogrammi

Health hazard
GHS08

Avvertenze

Warning

Indicazioni di pericolo

H351

Classi di pericolo

Carc. 2

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 1

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

dust mask type N95 (US), Eyeshields, Gloves

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Certificati d'analisi (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.
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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
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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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