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Sigma-Aldrich

Nitroethane

ReagentPlus®, 99.5%

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About This Item

Fórmula linear:
CH3CH2NO2
Número CAS:
79-24-3
Peso molecular:
75.07
Beilstein:
1209324
Número CE:
201-188-9
Número MDL:
MFCD00007404
Código UNSPSC:
12352102
ID de substância PubChem:
329752345

densidade de vapor

2.58 (vs air)

pressão de vapor

15.6 mmHg ( 20 °C)

linha de produto

ReagentPlus®

Ensaio

99.5%

forma

liquid

temperatura de autoignição

778 °F

Lim. expl.

3.4 %

índice de refração

n20/D 1.391 (lit.)

pb

114-115 °C (lit.)

pf

−90 °C (lit.)

solubilidade

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

densidade

1.045 g/mL at 25 °C (lit.)

cadeia de caracteres SMILES

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

InChI

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

chave InChI

MCSAJNNLRCFZED-UHFFFAOYSA-N

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Informações legais

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

Palavra indicadora

Warning

Classificações de perigo

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

Código de classe de armazenamento

3 - Flammable liquids

Classe de risco de água (WGK)

WGK 2

Ponto de fulgor (°F)

87.8 °F - closed cup

Ponto de fulgor (°C)

31 °C - closed cup

Certificados de análise (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
Dan T Major et al.
Journal of the American Chemical Society, 127(47), 16374-16375 (2005-11-25)
We have carried out a mixed molecular dynamics and centroid path integral simulation using a combined quantum mechanical and molecular mechanical (QM/MM) potential to study the anomalous Brønsted relationship between rates and equilibria for deprotonation of nitroalkanes in water, which
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
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
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