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Sigma-Aldrich

Nitroethan

ReagentPlus®, 99.5%

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About This Item

Lineare Formel:
CH3CH2NO2
CAS-Nummer:
79-24-3
Molekulargewicht:
75.07
Beilstein:
1209324
EG-Nummer:
201-188-9
MDL-Nummer:
MFCD00007404
UNSPSC-Code:
12352102
PubChem Substanz-ID:
329752345

Dampfdichte

2.58 (vs air)

Dampfdruck

15.6 mmHg ( 20 °C)

Produktlinie

ReagentPlus®

Assay

99.5%

Form

liquid

Selbstzündungstemp.

778 °F

Expl.-Gr.

3.4 %

Brechungsindex

n20/D 1.391 (lit.)

bp

114-115 °C (lit.)

mp (Schmelzpunkt)

−90 °C (lit.)

Löslichkeit

acetone: soluble(lit.)
alcohol: soluble(lit.)
water: slightly soluble(lit.)

Dichte

1.045 g/mL at 25 °C (lit.)

SMILES String

CC[N+]([O-])=O

InChI

1S/C2H5NO2/c1-2-3(4)5/h2H2,1H3

InChIKey

MCSAJNNLRCFZED-UHFFFAOYSA-N

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Rechtliche Hinweise

ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany

Signalwort

Warning

Gefahreneinstufungen

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

Lagerklassenschlüssel

3 - Flammable liquids

WGK

WGK 2

Flammpunkt (°F)

87.8 °F - closed cup

Flammpunkt (°C)

31 °C - closed cup

Analysenzertifikate (COA)

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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
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)
R C Anderson et al.
Bioresource technology, 97(18), 2421-2426 (2005-11-24)
Strategies are sought to reduce economic and environmental costs associated with ruminant methane emissions. The effect of oral nitroethane or 2-nitropropanol administration on ruminal methane-producing activity and volatile fatty acid production was evaluated in mature ewes. Daily administration of 24
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