00160
Acetamide
≥99.0% (GC)
동의어(들):
Amide C2
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크기 선택
제품정보 (DICE 배송 시 비용 별도)
Linear Formula:
CH3CONH2
CAS 번호:
Molecular Weight:
59.07
Beilstein:
1071207
EC Number:
MDL number:
UNSPSC 코드:
12352111
eCl@ss:
39031237
PubChem Substance ID:
NACRES:
NA.77
vapor pressure
1 mmHg ( 65 °C)
Quality Level
분석
≥99.0% (GC)
양식
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
유전자 정보
rat ... Ggt1(116568)
유사한 제품을 찾으십니까? 방문 제품 비교 안내
애플리케이션
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.
신호어
Warning
유해 및 위험 성명서
Hazard Classifications
Carc. 2
Storage Class Code
11 - Combustible Solids
WGK
WGK 1
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
개인 보호 장비
dust mask type N95 (US), Eyeshields, Gloves
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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