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Merck

00160

Sigma-Aldrich

乙酰胺

≥99.0% (GC)

别名:

C2 酰胺

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About This Item

线性分子式:
CH3CONH2
CAS号:
分子量:
59.07
Beilstein:
1071207
EC號碼:
MDL號碼:
分類程式碼代碼:
12352111
eCl@ss:
39031237
PubChem物質ID:
NACRES:
NA.77

蒸汽壓力

1 mmHg ( 65 °C)

品質等級

化驗

≥99.0% (GC)

形狀

crystals

bp

221 °C (lit.)

mp

78-80 °C (lit.)
78-82 °C

溶解度

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 字串

CC(N)=O

InChI

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

InChI 密鑰

DLFVBJFMPXGRIB-UHFFFAOYSA-N

基因資訊

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應用

乙酰胺用作生长培养基的补充剂和 tlyA 转座突变体的互补品。将该产品作为冷冻保护剂溶液的成分,从而通过玻璃化研究牛卵母细胞的超微结构变化。

象形圖

Health hazard

訊號詞

Warning

危險聲明

危險分類

Carc. 2

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 1

閃點(°F)

Not applicable

閃點(°C)

Not applicable

個人防護裝備

dust mask type N95 (US), Eyeshields, Gloves


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分析证书(COA)

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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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