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Merck
CN

227870

Nitroethane

ReagentPlus®, 99.5%

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About This Item

Linear Formula:
CH3CH2NO2
CAS Number:
79-24-3
Molecular Weight:
75.07
EC Number:
201-188-9
UNSPSC Code:
12352102
PubChem Substance ID:
329752345
Beilstein/REAXYS Number:
1209324
MDL number:
MFCD00007404
Assay:
99.5%
Bp:
114-115 °C (lit.)
Vapor pressure:
15.6 mmHg ( 20 °C)

Key Documents

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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

100

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

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Warning

Hazard Classifications

Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Aquatic Chronic 3 - Flam. Liq. 3 - Repr. 2

Storage Class

3 - Flammable liquids

wgk

WGK 2

flash_point_f

87.8 °F - closed cup

flash_point_c

31 °C - closed cup

Regulatory Information

危险化学品
易制爆化学品
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Certificates of Analysis (COA)

Lot/Batch Number
MKBN5177V
MKBL6151V
MKBJ3670V

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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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