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73478

Sigma-Aldrich

Nitromethane

puriss., absolute, over molecular sieve, ≥98.5% (GC)

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About This Item

Empirical Formula (Hill Notation):
CH3NO2
CAS Number:
Molecular Weight:
61.04
Beilstein/REAXYS Number:
1698205
EC Number:
MDL number:
UNSPSC Code:
12352102
PubChem Substance ID:
NACRES:
NA.21
assay:
≥98.5% (GC)
bp:
101.2 °C (lit.)
vapor pressure:
2.7 mmHg

vapor density

2.1 (vs air)

Quality Level

vapor pressure

2.7 mmHg

grade

absolute
puriss.

assay

≥98.5% (GC)

form

liquid

autoignition temp.

784 °F

quality

over molecular sieve

expl. lim.

7.3 %, 33 °F

impurities

≤0.01% water
water

refractive index

n20/D 1.382 (lit.)
n20/D 1.382

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.)

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.[1] It undergoes Michael addition reaction with chalcones in the presence of cinchona alkaloid-derived chiral bifunctional thiourea organocatalyst.[2] Its conversion to N2 in the presence of Co-ZSM5 (Zeolite Socony Mobil-5) has been studied.[3]

Application

Nitromethane may be employed in the preparation of cobalt cage complexes.[4]

signalword

Warning

Hazard Classifications

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

Storage Class

4.1A - Other explosive hazardous materials

wgk_germany

WGK 2

flash_point_f

95.0 °F - closed cup

flash_point_c

35 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter


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Customers Also Viewed

Metal ion encapsulation: cobalt cages derived from polyamines, formaldehyde, and nitromethane.
Geue RJ, et al.
Journal of the American Chemical Society, 106(19), 5478-5488 (1984)
The catalytic chemistry of nitromethane over Co-ZSM5 and other catalysts in connection with the methane-NOxSCR reaction.
Cowan AD, et al.
J. Catal., 176(2), 329-343 (1998)
F Ferreira da Silva et al.
The Journal of chemical physics, 135(17), 174504-174504 (2011-11-11)
Results of a detailed study on electron interactions with nitromethane (CH(3)NO(2)) embedded in helium nanodroplets are reported. Anionic and cationic products formed are analysed by mass spectrometry. When the doped helium droplets are irradiated with low-energy electrons of about 2
Construction of an all-carbon quaternary stereocenter by the peptide-catalyzed asymmetric Michael addition of nitromethane to β-disubstituted α,β-unsaturated aldehydes.
Kengo Akagawa et al.
Angewandte Chemie (International ed. in English), 51(51), 12786-12789 (2012-11-13)
Ryan R Walvoord et al.
Organic letters, 14(16), 4086-4089 (2012-07-31)
An efficient cross-coupling reaction of aryl halides and nitromethane was developed with the use of parallel microscale experimentation. The arylnitromethane products are precursors for numerous useful synthetic products. An efficient method for their direct conversion to the corresponding oximes and

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