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227870

Sigma-Aldrich

Nitroethane

ReagentPlus®, 99.5%

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About This Item

Formula condensata:
CH3CH2NO2
Numero CAS:
Peso molecolare:
75.07
Beilstein:
1209324
Numero CE:
Numero MDL:
Codice UNSPSC:
12352102
ID PubChem:

Densità del vapore

2.58 (vs air)

Tensione di vapore

15.6 mmHg ( 20 °C)

Nome Commerciale

ReagentPlus®

Saggio

99.5%

Forma fisica

liquid

Temp. autoaccensione

778 °F

Limite di esplosione

3.4 %

Indice di rifrazione

n20/D 1.391 (lit.)

P. eboll.

114-115 °C (lit.)

Punto di fusione

−90 °C (lit.)

Solubilità

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

Densità

1.045 g/mL at 25 °C (lit.)

Stringa SMILE

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

InChI

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

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Note legali

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

Avvertenze

Warning

Indicazioni di pericolo

Classi di pericolo

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

Codice della classe di stoccaggio

3 - Flammable liquids

Classe di pericolosità dell'acqua (WGK)

WGK 2

Punto d’infiammabilità (°F)

87.8 °F - closed cup

Punto d’infiammabilità (°C)

31 °C - closed cup


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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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