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108170

Sigma-Aldrich

Nitromethane

reagent grade, 96%

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About This Item

Formula empirica (notazione di Hill):
CH3NO2
Numero CAS:
75-52-5
Peso molecolare:
61.04
Beilstein:
1698205
Numero CE:
200-876-6
Numero MDL:
MFCD00007400
Codice UNSPSC:
12352102
ID PubChem:
57646805

Grado

reagent grade

Densità del vapore

2.1 (vs air)

Tensione di vapore

2.7 mmHg

Saggio

96%

Forma fisica

liquid

Temp. autoaccensione

784 °F

Limite di esplosione

7.3 %, 33 °F

Indice di rifrazione

n20/D 1.382 (lit.)

P. eboll.

101.2 °C (lit.)

Punto di fusione

−29 °C (lit.)

Densità

1.127 g/mL at 25 °C (lit.)

Stringa SMILE

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

InChI

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

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Altre note

A -D suffix exists for administrative purposes only.
All -D packages are 100% the same product, same quality, same specification as the package sizes previously sold without a -D.

Avvertenze

Warning

Indicazioni di pericolo

H226,H302 + H332,H351,H361d

Classi di pericolo

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

Codice della classe di stoccaggio

4.1A - Other explosive hazardous materials

Classe di pericolosità dell'acqua (WGK)

WGK 2

Punto d’infiammabilità (°F)

95.0 °F - closed cup

Punto d’infiammabilità (°C)

35 °C - closed cup

Dispositivi di protezione individuale

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

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Certificati d'analisi (COA)

Lot/Batch Number
MKAA2805V
MKBC1544V
BCBG0031V
BCBF6848V
BCBC9416V

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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)
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.
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
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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