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31567

Supelco

2-Nitrotoluene

analytical standard

Synonym(s):

1-Methyl-2-nitrobenzene

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About This Item

Linear Formula:
CH3C6H4NO2
CAS Number:
88-72-2
Molecular Weight:
137.14
Beilstein/REAXYS Number:
1907580
EC Number:
201-853-3
MDL number:
MFCD00007157
UNSPSC Code:
41116107
PubChem Substance ID:
329753820
NACRES:
NA.24

grade

analytical standard

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

refractive index

n20/D 1.546 (lit.)

bp

225 °C (lit.)

mp

−4-−3 °C (lit.)

density

1.163 g/mL at 25 °C (lit.)

application(s)

cleaning products
cosmetics
environmental
food and beverages
personal care

format

neat

SMILES string

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

InChI

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

InChI key

PLAZTCDQAHEYBI-UHFFFAOYSA-N

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Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

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Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.

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Danger

Hazard Classifications

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

Storage Class

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

wgk_germany

WGK 3

flash_point_f

203.0 °F - closed cup

flash_point_c

95 °C - closed cup

ppe

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

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Certificates of Analysis (COA)

Lot/Batch Number
BCBV8248

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Akané E Hartenbach et al.
Environmental science & technology, 42(22), 8352-8359 (2008-12-17)
Compound-specific nitrogen isotope analysis was shown to be a promising tool for the quantitative assessment of abiotic reduction of nitroaromatic contaminants (NACs) under anoxic conditions. To assess the magnitude and variability of 15N fractionation for reactions with dissolved reductants, we
H L Hong et al.
Toxicology and applied pharmacology, 191(3), 227-234 (2003-09-19)
The most prominent neoplastic lesions in mice in the 2-year studies of o-nitrotoluene and riddelliine were hemangiosarcomas. Fifteen o-nitrotoluene-induced hemangiosarcomas of the skeletal muscle, subcutaneous tissue, and mesentery; 12 riddelliine-induced hemangiosarcomas of the liver; and 15 spontaneous subcutaneous hemangiosarcomas were
Sikandar I Mulla et al.
Biodegradation, 22(1), 95-102 (2010-06-29)
A bacterial consortium capable of degrading nitroaromatic compounds was isolated from pesticide-contaminated soil samples by selective enrichment on 2-nitrotoluene as a sole source of carbon and energy. The three different bacterial isolates obtained from bacterial consortium were identified as Bacillus
Ismael Cotte-Rodríguez et al.
The Analyst, 130(5), 679-686 (2005-04-27)
The use of two methods in tandem, single-sided membrane introduction mass spectrometry (SS-MIMS) and fiber introduction mass spectrometry (FIMS), is presented as a technique for field analysis. The combined SS-MIMS-FIMS technique was employed in both a modified commercial mass spectrometer
Sikandar I Mulla et al.
Chemosphere, 90(6), 1920-1924 (2012-11-17)
Nitrotoluenes are the toxic pollutants of the environment because of their large scale use in the production of explosives. Biodegradation of such chemicals by microorganisms may provide an effective method for their detoxification. We have studied the degradation of 2-nitrotoluene
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