227870
硝基乙烷
ReagentPlus®, 99.5%
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关于此项目
线性分子式:
CH3CH2NO2
化学文摘社编号:
分子量:
75.07
EC Number:
201-188-9
UNSPSC Code:
12352102
PubChem Substance ID:
Beilstein/REAXYS Number:
1209324
MDL number:
Assay:
99.5%
Bp:
114-115 °C (lit.)
Vapor pressure:
15.6 mmHg ( 20 °C)
InChI key
MCSAJNNLRCFZED-UHFFFAOYSA-N
InChI
1S/C2H5NO2/c1-2-3(4)5/h2H2,1H3
SMILES string
CC[N+]([O-])=O
vapor density
2.58 (vs air)
vapor pressure
15.6 mmHg ( 20 °C)
product line
ReagentPlus®
assay
99.5%
form
liquid
autoignition temp.
778 °F
expl. lim.
3.4 %
dilution
(for general lab use)
Quality Level
bp
114-115 °C (lit.)
mp
−90 °C (lit.)
solubility
acetone: soluble(lit.), alcohol: soluble(lit.), water: slightly soluble(lit.)
density
1.045 g/mL at 25 °C (lit.)
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Legal Information
ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany
signalword
Warning
Hazard Classifications
Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Aquatic Chronic 3 - Flam. Liq. 3 - Repr. 2
存储类别
3 - Flammable liquids
wgk
WGK 2
flash_point_f
87.8 °F - closed cup
flash_point_c
31 °C - closed cup
法规信息
危险化学品
易制爆化学品
此项目有
Feng-Wu Liu et al.
Carbohydrate research, 344(18), 2439-2443 (2009-11-03)
Henry reactions of a novel higher sugar derivative, (1R)-(1,4:3,6-dianhydro-D-mannitol-2-yl)-1,4:3,6-dianhydro-D-fructose 5,5'-dinitrate (Alternate nomenclature: (1R)-(isomannid-2-yl)-1,4:3,6-dianhydro-D-fructose 5,5'-dinitrate), with nitromethane and nitroethane were studied. The kinetic and thermodynamic reactions with nitromethane under different conditions were carried out to afford (2S)- and (2R)-beta-nitroalcohols, respectively. But
S T Stokes et al.
The Journal of chemical physics, 129(6), 064308-064308 (2008-08-22)
Valence and dipole-bound negative ions of the nitroethane (NE) molecule and its clusters are studied using photoelectron spectroscopy (PES), Rydberg electron transfer (RET) techniques, and ab initio methods. Valence adiabatic electron affinities (EA(a)s) of NE, C(2)H(5)NO(2), and its clusters, (C(2)H(5)NO(2))(n)
Kevin Francis et al.
Biochemistry, 47(35), 9136-9144 (2008-08-12)
The deprotonation of nitroethane catalyzed by Neurospora crassa 2-nitropropane dioxygenase was investigated by measuring the formation and release of ethylnitronate formed in turnover as a function of pH and through mutagenesis studies. Progress curves for the enzymatic reaction obtained by
Paul F Fitzpatrick et al.
Archives of biochemistry and biophysics, 433(1), 157-165 (2004-12-08)
While several flavoproteins will oxidize nitroalkanes in addition to their physiological substrates, nitroalkane oxidase (NAO) is the only one which does not require the anionic nitroalkane. This, in addition to the induction of NAO by nitroethane seen in Fusarium oxysporum
A K Bozic et al.
Bioresource technology, 100(17), 4017-4025 (2009-04-14)
The effects of several methane-inhibitors on rumen fermentation were compared during three 24h consecutive batch cultures of ruminal microbes in the presence of nonlimiting amounts of hydrogen. After the initial incubation series, methane production was reduced greater than 92% from
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