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00160

Sigma-Aldrich

Acetamid

≥99.0% (GC)

Synonym(e):

Amid C2

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About This Item

Lineare Formel:
CH3CONH2
CAS-Nummer:
60-35-5
Molekulargewicht:
59.07
Beilstein:
1071207
EG-Nummer:
200-473-5
MDL-Nummer:
MFCD00008023
UNSPSC-Code:
12352111
eCl@ss:
39031237
PubChem Substanz-ID:
329747009
NACRES:
NA.77

Dampfdruck

1 mmHg ( 65 °C)

Qualitätsniveau

200

Assay

≥99.0% (GC)

Form

crystals

bp

221 °C (lit.)

mp (Schmelzpunkt)

78-80 °C (lit.)
78-82 °C

Löslichkeit

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)

InChIKey

DLFVBJFMPXGRIB-UHFFFAOYSA-N

Angaben zum Gen

rat ... Ggt1(116568)

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Anwendung

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.

Piktogramme

Health hazard
GHS08

Signalwort

Warning

H-Sätze

H351

Gefahreneinstufungen

Carc. 2

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 1

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

dust mask type N95 (US), Eyeshields, Gloves

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Analysenzertifikate (COA)

Lot/Batch Number

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Succinamid 98%

Sigma-Aldrich

124753

Succinamid

Isovaleraldehyd 97%

Sigma-Aldrich

146455

Isovaleraldehyd

tert-Butanol analytical standard

Supelco

50621

tert-Butanol

Cäsiumbromid 99.999% trace metals basis

Sigma-Aldrich

203017

Cäsiumbromid

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
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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
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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
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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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