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360554

Sigma-Aldrich

Nitromethane

ACS reagent, ≥95%

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About This Item

Empirical Formula (Hill Notation):
CH3NO2
CAS Number:
Molecular Weight:
61.04
Beilstein:
1698205
EC Number:
MDL number:
UNSPSC Code:
12352102
PubChem Substance ID:
NACRES:
NA.21

grade

ACS reagent

Quality Level

vapor density

2.1 (vs air)

vapor pressure

2.7 mmHg ( 20 °C)

Assay

≥95%

form

liquid

autoignition temp.

784 °F

expl. lim.

7.3 %, 33 °F

impurities

≤0.05% water

color

APHA: ≤10

refractive index

n20/D 1.382 (lit.)

pH

6.4 (20 °C, 0.01 g/L)

bp

101.2 °C (lit.)

mp

−29 °C (lit.)

density

1.127 g/mL at 25 °C (lit.)

suitability

clear for appearance

SMILES string

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

InChI

1S/CH3NO2/c1-2(3)4/h1H3

InChI key

LYGJENNIWJXYER-UHFFFAOYSA-N

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General description

Nitromethane is an aliphatic nitro compound that is commonly used as a solvent for chemical processing and analysis.

Application

Nitromethane can be used as a solvent in the:
  • FeCl3-catalyzed Friedel-Crafts alkylation of indoles with alcohols.
  • Cobalt-catalyzed dehydration of aldoximes to nitriles.
  • Chemoselective oxidation of alcohols to carbonyl compounds.
  • Gold-catalyzed hydroarylation of aryl-substituted alkynes.

Signal Word

Warning

Hazard Classifications

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

Storage Class Code

4.1A - Other explosive hazardous materials

WGK

WGK 2

Flash Point(F)

95.0 °F - closed cup

Flash Point(C)

35 °C - closed cup


Certificates of Analysis (COA)

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The catalytic chemistry of nitromethane over Co-ZSM5 and other catalysts in connection with the methane-NOxSCR reaction.
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J. Catal., 176(2), 329-343 (1998)
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Cinchona alkaloid-derived chiral bifunctional thiourea organocatalysts were synthesized and applied in the Michael addition between nitromethane and chalcones with high ee and chemical yields.
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In this study, the effects of pH, bromide and nitrite on the formation of halonitromethanes (HNMs) and trihalomethanes (THMs) from eight amino acids (glycine, alanine, serine, cysteine, aspartic acid, glutamic acid, lysine and histidine) and four amino sugars (glucosamine, galactosamine
Huachang Hong et al.
The Science of the total environment, 444, 196-204 (2012-12-29)
The formations of THMs, HAAs, and HNMs from chlorination and chloramination of water from Jinlan Reservoir were investigated in this study. Results showed that monochloramine rather than chlorine generally resulted in lower concentration of DBPs, and the DBPs formation varied

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