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线性分子式:
HCONH2
化学文摘社编号:
分子量:
45.04
UNSPSC Code:
12352111
NACRES:
NA.21
PubChem Substance ID:
EC Number:
200-842-0
Beilstein/REAXYS Number:
505995
MDL number:
Assay:
≥99.0% (GC)
Technique(s):
hybridization: suitable
Bp:
210 °C (lit.)
Vapor pressure:
0.08 mmHg ( 20 °C)
30 mmHg ( 129 °C)
30 mmHg ( 129 °C)
产品名称
甲酰胺, ReagentPlus®, ≥99.0% (GC)
SMILES string
NC=O
InChI key
ZHNUHDYFZUAESO-UHFFFAOYSA-N
InChI
1S/CH3NO/c2-1-3/h1H,(H2,2,3)
vapor density
1.55 (vs air)
vapor pressure
0.08 mmHg ( 20 °C)
30 mmHg ( 129 °C)
product line
ReagentPlus®
assay
≥99.0% (GC)
form
liquid
autoignition temp.
932 °F
expl. lim.
2.7-19 %
technique(s)
hybridization: suitable
refractive index
n20/D 1.447 (lit.)
pH
4-10 (20 °C, 200 g/L)
bp
210 °C (lit.)
mp
2-3 °C (lit.)
density
1.134 g/mL at 25 °C (lit.)
Quality Level
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Application
甲酰胺可作为溶剂用于:
- 通过二磷酸二氢二钠与三烷基氯硅烷的反应合成四(三烷基硅基)二磷酸。
- 叠氮化物与末端炔之间的 Cu/C 催化环加成反应,以合成三唑。
甲酰胺可使核酸双螺旋不稳定,通常可以 50% 的浓度,用于需要较低杂交温度的杂交实验。
General description
甲酰胺是一种极性溶剂,主要用于树脂和增塑剂。它可以由一氧化碳和氨直接合成。
Legal Information
ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany
signalword
Danger
hcodes
Hazard Classifications
Carc. 2 - Repr. 1B - STOT RE 2 Oral
target_organs
Blood
存储类别
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
wgk
WGK 1
flash_point_f
305.6 °F
flash_point_c
152 °C
The crystal structure of formamide.
Ladell J and Post B.
Acta Crystallographica, 7(8-9), 559-564 (1954)
Microwave spectrum, structure, dipole moment, and quadrupole coupling constants of formamide.
Kurland RJ and Wilson Jr EB.
J. Chem. Phys. , 27(2), 585-590 (1957)
The formamide method for the extraction of polysaccharides from haemolytic streptococci.
Fuller AT.
British Journal of Experimental Pathology, 19(2), 130-130 (1938)
The dynamics of liquid formamide, N-methylformamide, N,N-dimethylformamide, and N,N-dimethylacetamide. A dielectric relaxation study.
Barthel J, et al.
Journal of Molecular Liquids, 98, 51-69 (2002)
Penelope A Bryant et al.
PloS one, 6(5), e19556-e19556 (2011-06-10)
A central issue in the design of microarray-based analysis of global gene expression is that variability resulting from experimental processes may obscure changes resulting from the effect being investigated. This study quantified the variability in gene expression at each level
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