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438804

Sigma-Aldrich

2-Nitrotoluene

≥99%

Synonyme(s) :

1-Methyl-2-nitrobenzene

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About This Item

Formule linéaire :
CH3C6H4NO2
Numéro CAS:
88-72-2
Poids moléculaire :
137.14
Numéro Beilstein :
1907580
Numéro CE :
201-853-3
Numéro MDL:
MFCD00007157
Code UNSPSC :
12352100
ID de substance PubChem :
24867471
Nomenclature NACRES :
NA.22

Pureté

≥99%

Forme

liquid

Indice de réfraction

n20/D 1.546 (lit.)

Point d'ébullition

225 °C (lit.)

Pf

−4-−3 °C (lit.)

Densité

1.163 g/mL at 25 °C (lit.)

Chaîne SMILES 

Cc1ccccc1[N+]([O-])=O

InChI

1S/C7H7NO2/c1-6-4-2-3-5-7(6)8(9)10/h2-5H,1H3

Clé InChI

PLAZTCDQAHEYBI-UHFFFAOYSA-N

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Description générale

2-Nitrotoluene is a nitroaromatic compound. Multi-functional magnetic resins having high surface area and ion exchange efficiency (GMA30-1 and GMA30-2) were developed and were tested for the desorption of 2-nitrotolene. Its dioxygenation by nitrobenzene dioxygenase has been studied to evaluate the isotope fractionation. It has been reported as nitroaromatic explosive. Terbium-based magnetic metal-organic framework (MOF) nanospheres have been fabricated, which can detect the trace quantities of 2-nitrotoluene.

Application

2-Nitrotoluene may be employed as nitrogen supplement in the culture medium of Pseudomonas sp. strain ClS1. It may be employed as carbon and energy supplement in the culture medium of Pseudomonas sp. strain JS42.

Pictogrammes

Health hazardExclamation markEnvironment
GHS08,GHS07,GHS09

Mention d'avertissement

Danger

Mentions de danger

H302,H340,H350,H361f,H411

Classification des risques

Acute Tox. 4 Oral - Aquatic Chronic 2 - Carc. 1B - Muta. 1B - Repr. 2

Code de la classe de stockage

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

203.0 °F - closed cup

Point d'éclair (°C)

95 °C - closed cup

Équipement de protection individuelle

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

Certificats d'analyse (COA)

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Sigma-Aldrich

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E Duque et al.
Journal of bacteriology, 175(8), 2278-2283 (1993-04-01)
A bacterium, Pseudomonas sp. strain C1S1, able to grow on 2,4,6-trinitrotoluene (TNT), 2,4- and 2,6-dinitrotoluene, and 2-nitrotoluene as N sources, was isolated. The bacterium grew at 30 degrees C with fructose as a C source and accumulated nitrite. Through batch
Jing-Jing Qian et al.
Dalton transactions (Cambridge, England : 2003), 43(10), 3978-3983 (2014-01-24)
In this work, we present novel kinds of Fe3O4@Tb-BTC magnetic metal-organic framework (MOF) nanospheres which possess both magnetic characteristics and fluorescent properties using a layer by layer assembly technique. The structure and morphology of the as-prepared Fe3O4@Tb-BTC were systematically characterized
Wei Wang et al.
Journal of hazardous materials, 294, 158-167 (2015-04-14)
Two novel multi-functional magnetic resins named GMA30-1 and GMA30-2 were fabricated and investigated for the removal of 4-nitrotoluene-2-sulfonic acid (NTS) and 2-nitrotoluene (o-MNT). Strong base resin (GMA30-1) and weak base resin (GMA30-2) possess large surface area of 718m(2)/g and 559m(2)/g
Sarah G Pati et al.
Environmental science & technology, 48(18), 10750-10759 (2014-08-08)
Oxygenation of aromatic rings is a frequent initial step in the biodegradation of persistent contaminants, and the accompanying isotope fractionation is increasingly used to assess the extent of transformation in the environment. Here, we systematically investigated the dioxygenation of two
D An et al.
Journal of bacteriology, 176(24), 7462-7467 (1994-12-01)
Pseudomonas sp. strain JS42 utilizes 2-nitrotoluene (2NT) as the sole source of carbon and energy for growth. Intact cells catalyze the oxidation of 2NT to 3-methylcatechol and nitrite in a reaction that requires molecular oxygen. Cell extracts oxidized 2NT to
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