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• Solvents and Organic Chemicals Organic Compounds Benzenoids Benzene and substituted derivatives Benzoyl derivatives

Benzaldehyde, 4-(methylamino)- (CAS No. 556-21-8): Properties, Applications, and Market Insights

Benzaldehyde, 4-(methylamino)- (CAS No. 556-21-8) is a specialized organic compound that has garnered significant attention in the chemical and pharmaceutical industries. Known for its unique aromatic properties and functional group versatility, this compound is widely utilized in various applications, ranging from pharmaceutical intermediates to flavor and fragrance formulations. Its molecular structure, featuring a benzaldehyde core with a methylamino substituent at the para position, makes it a valuable building block in synthetic chemistry.

The chemical properties of Benzaldehyde, 4-(methylamino)- include a molecular formula of C8H9NO and a molecular weight of 135.16 g/mol. It typically appears as a pale yellow to light brown liquid with a distinct aromatic odor. The compound's solubility in organic solvents like ethanol, acetone, and dichloromethane makes it highly adaptable for laboratory and industrial processes. Researchers often highlight its role in Schiff base formation, a reaction pivotal in the synthesis of bioactive compounds and coordination chemistry.

One of the most prominent applications of Benzaldehyde, 4-(methylamino)- is in the pharmaceutical sector. It serves as a key intermediate in the synthesis of antihistamines, antidepressants, and other central nervous system (CNS) drugs. Recent studies have explored its potential in cancer research, particularly in the development of tyrosine kinase inhibitors, which are critical for targeted cancer therapies. This aligns with the growing demand for precision medicine and personalized treatment options, topics that are currently trending in healthcare discussions.

In addition to pharmaceuticals, Benzaldehyde, 4-(methylamino)- finds applications in the flavor and fragrance industry. Its aromatic profile contributes to the formulation of synthetic flavors and perfume bases. With consumers increasingly seeking natural-like and sustainable fragrance alternatives, this compound's role in mimicking natural aromas has become more relevant. Industry experts are also investigating its use in green chemistry initiatives, which aim to reduce environmental impact through safer chemical processes.

The market dynamics for Benzaldehyde, 4-(methylamino)- reflect its growing importance. According to recent reports, the global demand for fine chemicals and pharmaceutical intermediates is expected to rise, driven by advancements in drug discovery and biotechnology. Manufacturers are focusing on high-purity production methods to meet the stringent requirements of the pharmaceutical grade market. Additionally, the compound's compatibility with continuous flow chemistry—a hot topic in modern chemical engineering—has positioned it as a candidate for scalable synthesis.

From a research perspective, Benzaldehyde, 4-(methylamino)- continues to be a subject of interest in organic synthesis and material science. Its ability to act as a ligand in metal-organic frameworks (MOFs) has opened new avenues for applications in gas storage and catalysis. Researchers are also exploring its potential in photocatalysis, a field gaining traction due to its relevance in renewable energy solutions.

For those seeking safety data on Benzaldehyde, 4-(methylamino)-, it is essential to consult reliable sources like Material Safety Data Sheets (MSDS) or chemical regulatory databases. Proper handling, storage, and disposal procedures should always be followed to ensure workplace safety and environmental compliance. As with any chemical compound, understanding its toxicological profile and exposure limits is critical for safe usage.

In summary, Benzaldehyde, 4-(methylamino)- (CAS No. 556-21-8) is a multifaceted compound with significant applications in pharmaceuticals, flavors and fragrances, and advanced materials. Its relevance in cutting-edge research and industrial processes underscores its value in modern chemistry. As the demand for specialty chemicals continues to grow, this compound is poised to play an even more prominent role in scientific and commercial advancements.

• 332411-18-4(4-(Di-M-Tolyl-Amino)-Benzaldehyde)
• 119001-43-3(NTBA)
• 173471-71-1(6-(dimethylamino)naphthalene-2-carbaldehyde)
• 7541-76-6(4-Formyl-N,N,N-trimethylbenzenaminium iodide)
• 100727-07-9(4-(phenylamino)benzaldehyde)
• 42906-19-4(4-(Di-p-tolyl-amino)-benzaldehyde)
• 4181-05-9(4-(N,N-Diphenylamino)benzaldehyde)
• 100-10-7(p-Dimethylaminobenzaldehyde)
• 53566-95-3(Bis(4-formylphenyl)phenylamine)
• 619-22-7(3-(Dimethylamino)benzaldehyde)