Skip to Content
Merck
CN
All Photos(1)

Documents

115843

Sigma-Aldrich

2-Methyl-3-nitroaniline

97%

Sign Into View Organizational & Contract Pricing
All Photos(1)
Synonym(s):
2-Amino-6-nitrotoluene, 3-Nitro-o-toluidine
Linear Formula:
CH3C6H3(NO2)NH2
CAS Number:
603-83-8
Molecular Weight:
152.15
Beilstein:
388393
EC Number:
210-059-6
MDL number:
MFCD00007731
UNSPSC Code:
12352100
PubChem Substance ID:
24847243
NACRES:
NA.22

Quality Level

100

Assay

97%

form

solid

bp

305 °C (lit.)

mp

88-90 °C (lit.)

SMILES string

Cc1c(N)cccc1[N+]([O-])=O

InChI

1S/C7H8N2O2/c1-5-6(8)3-2-4-7(5)9(10)11/h2-4H,8H2,1H3

InChI key

HFCFJYRLBAANKN-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Related Categories

General description

2-Amino-6-nitrotoluene (2-Methyl-3-nitroaniline) exhibits a stripping voltammetric behaviour that has been studied using a C(18) modified, carbon paste electrode.

Application

2-Amino-6-nitrotoluene (2-Methyl-3-nitroaniline) has been used as a standard while evaluating the potential for degradation of nitroaromatic compounds by indigenous microorganisms.

Signal Word

Danger

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Aquatic Acute 1 - Aquatic Chronic 2 - STOT RE 2

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

P M Bradley et al.
Applied and environmental microbiology, 60(6), 2170-2175 (1994-06-01)
Microorganisms indigenous to surface soils and aquifer materials collected at a munitions-contaminated site transformed 2,4,6-trinitrotoluene (TNT), 2,4-dinitrotoluene (2,4-DNT), and 2,6-dinitrotoluene (2,6-DNT) to amino-nitro intermediates within 20 to 70 days. Carbon mineralization studies with both unlabeled (TNT, 2,4-DNT, and 2,6-DNT) and
C Faller et al.
Analytical and bioanalytical chemistry, 356(3-4), 279-283 (1996-09-01)
The stripping voltammetric behaviour of Ioxynil and 2-methyl-3-nitroaniline has been studied by means of a C(18) modified carbon paste electrode. The analytes are preconcentrated under open-circuit conditions (Ioxynil at pH 3.9; 2-methyl-3-nitroaniline at pH 10). For the determination of Ioxynil
[Different frequency of induction of liver tumors in reciprocal murine hybrids].
V I Kaledin et al.
Doklady Akademii nauk, 348(1), 129-131 (1996-05-01)
G L Kedderis et al.
Biochemical and biophysical research communications, 113(2), 433-438 (1983-06-15)
Inhibition studies were used to investigate the identity of the microsomal enzyme(s) responsible for the NADPH-dependent N-hydroxylation of 2-amino-6-nitrotoluene. The N-hydroxylation reaction was inhibited by several cytochrome P-450 inhibitors as well as by methimazole, a substrate for flavin-containing monooxygenase. Heat
Zhenggong Wang et al.
ChemSusChem, 11(16), 2744-2751 (2018-05-29)
Polyimide-based materials provide attractive chemistries for the development of gas-separation membranes. Modification of inter- and intra-chain interactions is a route to improve the separation performance. In this work, copolyimides with Tröger's base (TB) monomers are designed and synthesized. In particular

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service