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Key Documents

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N27314

Sigma-Aldrich

3-Nitrotoluene

99%

Sinónimos:

1-Methyl-3-nitrobenzene

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About This Item

Fórmula lineal:
CH3C6H4NO2
Número de CAS:
99-08-1
Peso molecular:
137.14
Beilstein/REAXYS Number:
1906910
EC Number:
202-728-6
MDL number:
MFCD00007265
UNSPSC Code:
12352100
PubChem Substance ID:
24897588
NACRES:
NA.22

vapor density

4.73 (vs air)

vapor pressure

1 mmHg ( 50.2 °C)

assay

99%

form

liquid

refractive index

n20/D 1.541 (lit.)

bp

230-231 °C (lit.)

mp

14-16 °C (lit.)

density

1.157 g/mL at 25 °C (lit.)

SMILES string

Cc1cccc(c1)[N+]([O-])=O

InChI

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

InChI key

QZYHIOPPLUPUJF-UHFFFAOYSA-N

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signalword

Warning

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Chronic 2 - STOT RE 2

Storage Class

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

wgk_germany

WGK 3

flash_point_f

208.4 °F

flash_point_c

98 °C

ppe

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

Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

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Nitrobenzene ACS reagent, ≥99.0%

Sigma-Aldrich

252379

Nitrobenzene

Methyl 3-nitrobenzoate 99%

Sigma-Aldrich

155977

Methyl 3-nitrobenzoate

Valeric acid ≥99%

Sigma-Aldrich

240370

Valeric acid

Tolueno anhydrous, 99.8%

Sigma-Aldrich

244511

Tolueno

Ácido nítrico ACS reagent, 70%

Sigma-Aldrich

438073

Ácido nítrico

J Struijs et al.
The Science of the total environment, 57, 161-170 (1986-12-01)
The biodegradation of 2-, 3- and 4-nitrotoluene was investigated in a simple laboratory test. All three isomers are shown to be biodegradable in a die-away test after adaptation of the inoculum, though different results were obtained with different types of
J B Robertson et al.
Applied and environmental microbiology, 58(8), 2643-2648 (1992-08-01)
Pseudomonas putida F1 and Pseudomonas sp. strain JS150 initiate toluene degradation by incorporating molecular oxygen into the aromatic nucleus to form cis-1,2-dihydroxy-3-methylcyclohexa-3,5-diene. When toluene-grown cells were incubated with 2- and 3-nitrotoluene, the major products identified were 2- and 3-nitrobenzyl alcohol
D J Doolittle et al.
Cancer research, 43(6), 2836-2842 (1983-06-01)
The nitrotoluenes failed to induce unscheduled DNA synthesis in in vitro cultures of rat hepatocytes. Because intestinal bacteria are known to be involved in the metabolic activation of other nitroaromatic compounds, the genotoxicity of the nitrotoluenes was evaluated using an
B E Haigler et al.
Applied and environmental microbiology, 60(9), 3466-3469 (1994-09-01)
A strain of Pseudomonas sp. was isolated from nitrobenzene-contaminated soil and groundwater on 2-nitrotoluene as the sole source of carbon, energy, and nitrogen. Bacterial cells growing on 2-nitrotoluene released nitrite into the growth medium. The isolate also grew on 3-methylcatechol
L E Hallas et al.
Applied and environmental microbiology, 45(4), 1234-1241 (1983-04-01)
The transformation of mono- and dinitroaromatic compounds was measured in sewage effluent maintained under aerobic or anaerobic conditions. Most of the nitrobenzene, 3- and 4-nitrobenzoic acids, and 3- and 4-nitrotoluenes and much of the 1,2- and 1,3-dinitrobenzenes disappeared both in
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