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Merck

73478

Nitromethane

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

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100 ML

$231.00

$231.00


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About This Item

Empirical Formula (Hill Notation):
CH3NO2
CAS Number:
Molecular Weight:
61.04
UNSPSC Code:
12352102
NACRES:
NA.21
PubChem Substance ID:
EC Number:
200-876-6
Beilstein/REAXYS Number:
1698205
MDL number:
Assay:
≥98.5% (GC)
Technique(s):
GC/GC: suitable
Bp:
101.2 °C (lit.)
Vapor pressure:
2.7 mmHg

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Product Name

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

InChI key

LYGJENNIWJXYER-UHFFFAOYSA-N

InChI

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

SMILES string

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

vapor density

2.1 (vs air)

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

technique(s)

GC/GC: suitable

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.)

Quality Level

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1 of 4

This Item
2307311081708.20894
assay

≥98.5% (GC)

assay

≥99.0%

assay

96%

assay

≥98% (GC)

grade

absolute, puriss.

grade

-

grade

-

grade

-

Quality Level

100

Quality Level

200

Quality Level

-

Quality Level

200

form

liquid

form

liquid

form

liquid

form

liquid

expl. lim.

7.3 %, 33 °F

expl. lim.

7.3 %, 33 °F

expl. lim.

7.3 %, 33 °F

expl. lim.

7.3-63.0 % (v/v)

bp

101.2 °C (lit.)

bp

101.2 °C (lit.)

bp

101.2 °C (lit.)

bp

101.2 °C/1013 hPa

Application

Nitromethane may be employed in the preparation of cobalt cage complexes.[1]

General description

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

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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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)
Loay Awad
Experimental and therapeutic medicine, 19(3), 1835-1843 (2020-02-28)
Chemotherapy and radiation are unable to eliminate all cancer cells, particularly apoptosis-resistant cancer cells, despite their ability to kill cancer cluster cells. Thus, it is important to identify methods that eliminate all cancer cells in order to prevent relapse. Salinomycin
Benedek Vakulya et al.
Organic letters, 7(10), 1967-1969 (2005-05-07)
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.
Naomi Rom et al.
The journal of physical chemistry. A, 115(36), 10181-10202 (2011-08-05)
The decomposition mechanism of hot liquid nitromethane at various compressions was studied using reactive force field (ReaxFF) molecular dynamics simulations. A competition between two different initial thermal decomposition schemes is observed, depending on compression. At low densities, unimolecular C-N bond

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