• 1. Eco-friendly acetylcholine-carboxylate bio-ionic liquids for controllable N-methylation and N-formylation using ambient CO2 at low temperatures
  Wenfeng Zhao,Xiaoping Chi,Hu Li,Jian He,Jingxuan Long,Yufei Xu,Song Yang Green Chem. 2019 21 567
• 2. Ruthenium(ii) arene complexes bearing simple dioxime ligands: effective catalysts for the one-pot transfer hydrogenation/N-methylation of nitroarenes with methanol
  Roberta Colaiezzi,Chiara Saviozzi,Nicola di Nicola,Stefano Zacchini,Guido Pampaloni,Marcello Crucianelli,Fabio Marchetti,Andrea Di Giuseppe,Lorenzo Biancalana Catal. Sci. Technol. 2023 13 2160
• 3. Iron porphyrin-catalyzed N-trifluoroethylation of anilines with 2,2,2-trifluoroethylamine hydrochloride in aqueous solution
  Shuang Ren,Guiming Xu,Yongjia Guo,Qiang Liu,Cancheng Guo RSC Adv. 2021 11 20322
• 4. N-Methylation of ortho-substituted aromatic amines with methanol catalyzed by 2-arylbenzo[d]oxazole NHC–Ir(iii) complexes
  Shuang Huang,Xi Hong,He-Zhen Cui,Quan Zhou,Yue-Jian Lin,Xiu-Feng Hou Dalton Trans. 2019 48 5072
• 5. A rapid method for the in-field analysis of amphetamines employing the Agilent Bioanalyzer
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• Solvents and Organic Chemicals Organic Compounds Benzenoids Phenol ethers Aminophenyl ethers

2-Methoxy-N-methylaniline (CAS No. 10541-78-3): Properties, Applications, and Market Insights

2-Methoxy-N-methylaniline (CAS No. 10541-78-3), also known as N-methyl-2-methoxyaniline, is a versatile organic compound widely used in the chemical and pharmaceutical industries. This aromatic amine derivative is characterized by its methoxy and methylamino functional groups, which contribute to its unique chemical properties. The compound is often utilized as an intermediate in the synthesis of dyes, agrochemicals, and pharmaceutical ingredients.

The molecular formula of 2-Methoxy-N-methylaniline is C₈H₁₁NO, with a molecular weight of 137.18 g/mol. Its structure consists of a benzene ring substituted with a methoxy group (–OCH₃) at the ortho position and a methylamino group (–NHCH₃) at the same position. This configuration imparts specific reactivity, making it valuable for various synthetic applications. Researchers and manufacturers often seek high-purity 2-Methoxy-N-methylaniline for specialized reactions.

One of the key applications of 2-Methoxy-N-methylaniline is in the production of dyes and pigments. Its ability to act as a coupling agent in azo dye synthesis makes it indispensable for creating vibrant colors used in textiles, inks, and coatings. Additionally, the compound is employed in the development of pharmaceutical intermediates, where its structural features enable the synthesis of bioactive molecules. Recent trends show growing interest in sustainable synthesis methods for such intermediates, aligning with the global push for greener chemistry.

The market for 2-Methoxy-N-methylaniline is influenced by demand from the pharmaceutical and agrochemical sectors. With the rise of custom synthesis services, many companies now offer tailored solutions for this compound, ensuring high yields and purity. Analytical techniques like HPLC and GC-MS are commonly used to verify the quality of 2-Methoxy-N-methylaniline, addressing concerns about impurities and batch consistency.

From an environmental perspective, the handling and disposal of 2-Methoxy-N-methylaniline require adherence to safety guidelines. While not classified as highly hazardous, proper storage conditions—such as cool, dry environments away from oxidizing agents—are recommended to maintain stability. Regulatory frameworks like REACH and FDA guidelines often apply to its use in end products, particularly in pharmaceuticals.

Innovations in catalytic processes have recently improved the synthesis efficiency of 2-Methoxy-N-methylaniline. For example, researchers are exploring metal-free catalysts to reduce environmental impact. These advancements align with industry demands for cost-effective chemical production and reduced waste generation. Furthermore, the compound’s role in specialty chemicals continues to expand, with new patents highlighting its utility in advanced material science.

For those sourcing 2-Methoxy-N-methylaniline, it is essential to partner with reputable suppliers who provide detailed technical data sheets and certificates of analysis. Keywords such as buy 2-Methoxy-N-methylaniline and 10541-78-3 supplier are frequently searched in procurement databases, reflecting the compound’s commercial relevance. As the chemical industry evolves, 2-Methoxy-N-methylaniline remains a critical building block for innovation.

• 90043-09-7(Benzenamine, 2,4-dimethoxy-N-phenyl-)
• 7093-78-9(Benzenamine, N-(2,4-dimethoxyphenyl)-2,4-dimethoxy-)
• 7287-74-3(Benzenamine, 2-methoxy-N,N-bis(2-methoxyphenyl)-)
• 700-75-4(Benzenamine,2-methoxy-N,N-dimethyl-)
• 63338-69-2(1,4-Benzenediamine, N,N'-bis(methoxyphenyl)-)
• 10224-66-5(2,5-Dimethoxy-N-methylaniline)
• 600121-37-7(Benzenamine, 2,4,6-trimethoxy-N-methyl- (9CI))
• 70329-19-0(Benzenaminium,2-methoxy-N,N,N-trimethyl-, iodide (1:1))
• 5840-11-9(1,4-Benzenediamine,N1-(2-methoxyphenyl)-)
• 72066-78-5(1,4-Benzenediamine,2,5-dimethoxy-N1,N1-dimethyl-)