695122
Acetamide
sublimed, 99%
Synonym(s):
Amide C2
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About This Item
Linear Formula:
CH3CONH2
CAS Number:
Molecular Weight:
59.07
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
200-473-5
Beilstein/REAXYS Number:
1071207
MDL number:
Assay:
99%
Form:
sublimed
Product Name
Acetamide, sublimed, 99%
InChI
1S/C2H5NO/c1-2(3)4/h1H3,(H2,3,4)
InChI key
DLFVBJFMPXGRIB-UHFFFAOYSA-N
SMILES string
CC(N)=O
vapor pressure
1 mmHg ( 65 °C)
assay
99%
form
sublimed
bp
221 °C (lit.)
mp
78-80 °C (lit.)
functional group
amide
Quality Level
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Related Categories
signalword
Warning
hcodes
Hazard Classifications
Carc. 2
Storage Class
11 - Combustible Solids
wgk
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type P3 (EN 143) respirator cartridges
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E C B Silva et al.
Animal reproduction science, 132(3-4), 155-158 (2012-06-26)
The aim was to assess the in vitro effect of glycerol, ethylene glycol or acetamide on frozen-thawed ram spermatozoa. Aliquots of each sixteen ejaculates from four rams of the Morada Nova breed were diluted in Tris-egg yolk with glycerol (5%)
Asal Fallah-Tafti et al.
European journal of medicinal chemistry, 46(10), 4853-4858 (2011-08-20)
KX2-391 (KX-01/Kinex Pharmaceuticals), N-benzyl-2-(5-(4-(2-morpholinoethoxy)phenyl)pyridin-2-yl)acetamide, is a highly selective Src substrate binding site inhibitor. To understand better the role of pyridine ring and N-benzylsubstitution in KX2-391 and establish the structure-activity relationship, a number of N-benzyl substituted (((2-morpholinoethoxy)phenyl)thiazol-4-yl)acetamide derivatives containing thiazole instead
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
A E Alves et al.
Reproduction in domestic animals = Zuchthygiene, 47(6), 1003-1008 (2012-03-06)
This study was undertaken to compare cryotolerance, in terms of viability and resumption of meiosis after warming and culture (24 and 48 h), of ex situ (isolated) and in situ (enclosed in the ovarian tissue) feline cumulus-oocyte complexes (COCs) vitrified
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