≥95%(GC) for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Room temperature Ships Normal Check lot-specific COA for exact specifications.
SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
Cited in 2 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
N-Methyl-o-toluidine can be synthesized by reacting o-toluidine and benzotriazole.
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
| Pubchem Sid | 488184232 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/488184232 |
| Sonrisas canónicas | CC1=CC=CC=C1NC |
| IUPAC Name | N,2-dimethylaniline |
| InChIKey | GUAWMXYQZKVRCW-UHFFFAOYSA-N |
| INCHI | 1S/C8H11N/c1-7-5-3-4-6-8(7)9-2/h3-6,9H,1-2H3 |
| Isómeros SMILES | CC1=CC=CC=C1NC |
| WGK Alemania | 3 |
| Peso molecular | 121.18 |
| Beilstein | 12(3)1842 |
| Reaxy-Rn | 742175 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=742175&ln= |
Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS →Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA →Full quality attributes and acceptance criteria for this grade.
View spec sheet →Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Benzenoids |
| Clase | Benzene and substituted derivatives |
| Subclass | Toluenes |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Aminotoluenes |
| Alternative Parents | Phenylalkylamines Aniline and substituted anilines Secondary alkylarylamines Organopnictogen compounds Hydrocarbon derivatives |
| Molecular Framework | Aromatic homomonocyclic compounds |
| Substituents | Aminotoluene - Phenylalkylamine - Aniline or substituted anilines - Secondary aliphatic/aromatic amine - Secondary amine - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Organonitrogen compound - Amine - Aromatic homomonocyclic compound |
| Descripción | This compound belongs to the class of organic compounds known as aminotoluenes. These are organic aromatic compounds containing a benzene that carries a single methyl group and one amino group. |
| External Descriptors | Not available |
| Solubilidad | Solubility in water: Practically insoluble |
|---|---|
| Sensibilidad | Light Sensitive,Air Sensitive |
| Índice de refracción | 1.56 |
| Punto de inflamación (°F) | 174.2 °F |
| Punto de inflamación (°C) | 79°C |
| Punto de ebullición (°C) | 177-204 °C |
| Peso molecular | 121.180 g/mol |
| XLogP3 | 2.200 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 1 |
| Rotatable Bond Count | 1 |
| Exact Mass | 121.089 Da |
| Monoisotopic Mass | 121.089 Da |
| Topological Polar Surface Area | 12.000 Ų |
| Heavy Atom Count | 9 |
| Formal Charge | 0 |
| Complexity | 80.600 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 0 |
| Covalently-Bonded Unit Count | 1 |
| 1. Wenfeng Zhao, Xiaoping Chi, Hu Li, Jian He, Jingxuan Long, Yufei Xu, Song Yang. (2018) Eco-friendly acetylcholine-carboxylate bio-ionic liquids for controllable N-methylation and N-formylation using ambient CO2 at low temperatures. GREEN CHEMISTRY, 21 (3): (567-577). [PMID:] [10.1039/C8GC03549K] |
| 2. Yingzhuang Chen, Keyi Wang, Huihui Yang, Yixuan Liu, Shouzhuo Yao, Bo Chen, Lihua Nie, Guangming Xu. (2012) Synthesis of sulfo/vinyl biphasic silica hybrid monolithic capillary column and its application to on-column preconcentration for capillary electrochromatography. JOURNAL OF CHROMATOGRAPHY A, [PMID:22410157] [10.1016/j.chroma.2012.01.024] |
I1810020