All Photos(1)
Synonym(s):
2,N-Dimethylaniline, 2-Methyl-N-methylaniline, N,2-Dimethylaniline, N,2-Dimethylbenzenamine, N,o-Dimethylaniline, N-(2-Methylphenyl)methylamine, N-Methyl-2-methylaniline, N-Methyl-2-methylbenzenamine, N-Methyl-N-(o-tolyl)amine, N-Methyl-o-methylaniline, o,N-Dimethylaniline, Methyl(o-tolyl)amine, NSC 9395
Linear Formula:
CH3C6H4NHCH3
CAS Number:
Molecular Weight:
121.18
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
Assay
≥95%
bp
177-204 °C/740 mmHg (lit.)
density
0.981 g/mL at 25 °C (lit.)
SMILES string
CNc1ccccc1C
InChI
1S/C8H11N/c1-7-5-3-4-6-8(7)9-2/h3-6,9H,1-2H3
InChI key
GUAWMXYQZKVRCW-UHFFFAOYSA-N
General description
N-Methyl-o-toluidine can be synthesized by reacting o-toluidine and benzotriazole.
Application
N-Methyl-o-toluidine may be used in the preparation of 2-substituted N-methylindoles.
Reactant for:
- Palladium-catalyzed coupling reactions
- Palladium-catalyzed amination of bromoindazoles
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Aquatic Chronic 3 - STOT RE 2
WGK
WGK 3
Flash Point(F)
closed cup
Flash Point(C)
closed cup
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.
Jaakko Laakia et al.
Talanta, 132, 889-893 (2014-12-06)
Eight selected isomeric amines were ionized using atmospheric pressure chemical ionization and atmospheric pressure photoionization producing a protonated molecule [M+H](+) for each amine. The mobility of these ions was measured by ion mobility spectrometry. The amine compound class was shown
A Practical Synthetic Method for N-Methyl-o-Toluidine.
Katritzky AR and Akutagawa K.
Organic preparations and procedures international, 21(3), 340-341 (1989)
Carbon dioxide: a reagent for the simultaneous protection of nucleophilic centers and the activation of alternative locations to electrophilic attack. XVI, A novel synthetic method for the side-chain functionalization of N-methyl-o-toluidine and for the preparation of 2-substituted N-methylindoles.
Katritzky AR, et al.
Heterocycles, 30(1), 407-414 (1990)
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