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• Solvents and Organic Chemicals Organic Compounds Organoheterocyclic compounds Pyridines and derivatives Methylpyridines
• Pharmaceutical and Biochemical Products Medicinal Building Blocks Heterocyclic Building Blocks
• Solvents and Organic Chemicals Organic Compounds Heterocyclic Compounds
• Pharmaceutical and Biochemical Products Pharmaceutical Intermediates

Comprehensive Overview of 5-Ethyl-2-methylpyridine (CAS No. 104-90-5): Properties, Applications, and Industry Insights

5-Ethyl-2-methylpyridine (CAS No. 104-90-5), a versatile organic compound, belongs to the pyridine derivative family. Its molecular structure, featuring an ethyl group at the 5-position and a methyl group at the 2-position of the pyridine ring, grants it unique chemical properties. This compound is widely studied for its applications in pharmaceuticals, agrochemicals, and specialty chemicals. With the increasing demand for heterocyclic compounds in research and industrial processes, 5-Ethyl-2-methylpyridine has garnered significant attention.

One of the most frequently searched questions about 5-Ethyl-2-methylpyridine is its synthesis method. The compound is typically synthesized via condensation reactions or catalytic processes involving pyridine derivatives. Researchers often explore its solubility in organic solvents like ethanol, acetone, and dichloromethane, which is critical for its application in formulations. Additionally, its boiling point (approximately 180–185°C) and molecular weight (121.18 g/mol) are key physicochemical parameters for industrial use.

In the pharmaceutical sector, 5-Ethyl-2-methylpyridine serves as a building block for active pharmaceutical ingredients (APIs). Its structural motif is found in compounds with potential anti-inflammatory and antimicrobial properties. Recent trends in green chemistry have also spurred interest in optimizing its synthesis to reduce environmental impact, aligning with global sustainability goals.

The agrochemical industry leverages 5-Ethyl-2-methylpyridine in the development of crop protection agents. Its role as an intermediate in pesticide synthesis highlights its importance in enhancing agricultural productivity. With the rise of precision farming, demand for high-purity pyridine derivatives has surged, making this compound a focal point for manufacturers.

From a commercial perspective, 5-Ethyl-2-methylpyridine is traded as a fine chemical, with suppliers emphasizing high-purity grades (≥98%) for research and industrial applications. Analytical techniques like GC-MS and HPLC are commonly employed to verify its purity. The compound’s stability under standard storage conditions (room temperature, inert atmosphere) further enhances its usability.

Emerging applications of 5-Ethyl-2-methylpyridine include its use in electronic materials and catalysis. For instance, it acts as a ligand in transition metal complexes, which are pivotal in homogeneous catalysis. This aligns with the growing interest in energy-efficient chemical processes, a hot topic in modern chemistry.

Safety and handling of 5-Ethyl-2-methylpyridine are also frequently discussed. While it is not classified as hazardous under standard regulations, proper laboratory practices—such as using gloves and ventilation—are recommended. This aligns with broader industry shifts toward occupational safety and regulatory compliance.

In summary, 5-Ethyl-2-methylpyridine (CAS No. 104-90-5) is a multifaceted compound with expanding applications across diverse sectors. Its synthesis, properties, and industrial relevance make it a subject of ongoing research and commercial interest. As industries evolve toward sustainable and efficient solutions, this pyridine derivative is poised to play an increasingly vital role.

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• 27987-10-6(Pyridine, ethylmethyl-)
• 54119-29-8(Pyridine, 2,5-diethyl-)
• 702-16-9(Pyridine,5-butyl-2-methyl-)
• 62626-82-8(Pyridine, 2-methyl-5-(1-methylpropyl)-, (S)-)
• 73014-65-0(Pyridine, 5-ethyl-2,3-dimethyl-)
• 1006873-58-0(5-Ethyl-2-methylpyridine borane)
• 100189-17-1(2-(6-methylpyridin-3-yl)ethan-1-ol)
• 589-93-5(2,5-Lutidine)
• 710-40-7(Pyridine,5-hexyl-2-methyl-)