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227870

Sigma-Aldrich

Nitroethane

ReagentPlus®, 99.5%

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About This Item

Linear Formula:
CH3CH2NO2
CAS Number:
Molecular Weight:
75.07
Beilstein:
1209324
EC Number:
MDL number:
UNSPSC Code:
12352102
PubChem Substance ID:
Assay:
99.5%
bp:
114-115 °C (lit.)
vapor pressure:
15.6 mmHg ( 20 °C)

vapor density

2.58 (vs air)

Quality Level

vapor pressure

15.6 mmHg ( 20 °C)

product line

ReagentPlus®

Assay

99.5%

form

liquid

autoignition temp.

778 °F

expl. lim.

3.4 %

refractive index

n20/D 1.391 (lit.)

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.)

SMILES string

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

InChI

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

InChI key

MCSAJNNLRCFZED-UHFFFAOYSA-N

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Legal Information

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

Signal Word

Warning

Hazard Classifications

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

Storage Class Code

3 - Flammable liquids

WGK

WGK 2

Flash Point(F)

87.8 °F - closed cup

Flash Point(C)

31 °C - closed cup


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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)
Base-promoted diastereoselective addition of nitromethane and nitroethane to N-tert-butylsulfinyl imines: synthesis of N-protected α-amino acids and amino ketones.
Garcia-Mu?oz MJ, et al.
Tetrahedron Asymmetry, 25(4), 362-372 (2014)
Hector Gutierrez-Bañuelos et al.
Anaerobe, 13(1), 21-31 (2007-01-09)
Nitroethane inhibits the growth of certain zoonotic pathogens such as Campylobacter and Salmonella spp., foodborne pathogens estimated to cause millions of human infections each year, and enhances the Salmonella- and Escherichia coli-killing effect of an experimental chlorate product being developed
One-pot, three-component cascade synthesis of new tetrasubstituted pyrroles by coupling reaction of 2-functionally substituted 2-alkenals, amines, and nitroethane.
Keiko NA, et al.
Tetrahedron, 70(46), 8959-8970 (2014)

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