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• Solvents and Organic Chemicals Organic Compounds Organic nitrogen compounds Organonitrogen compounds Amines Primary amines

Comprehensive Overview of 1-Cyclopropylpropan-1-amine (CAS No. 219736-10-4): Properties, Applications, and Industry Insights

1-Cyclopropylpropan-1-amine (CAS No. 219736-10-4) is a specialized organic compound featuring a unique cyclopropyl ring attached to a propylamine backbone. This structural configuration endows it with distinct chemical properties, making it valuable in pharmaceutical research, agrochemical development, and material science. The compound's cyclopropyl group enhances its steric and electronic characteristics, which are critical for modulating biological activity or material performance. Researchers and industries increasingly focus on such amine derivatives due to their versatility in synthesizing bioactive molecules and functional materials.

In recent years, the demand for cyclopropyl-containing compounds like 1-cyclopropylpropan-1-amine has surged, driven by trends in drug discovery and sustainable chemistry. A 2023 study highlighted cyclopropylamines as key intermediates in designing kinase inhibitors and antiviral agents, aligning with global interest in targeted therapies. Additionally, the compound's potential in green chemistry applications—such as catalysts for CO₂ capture—has sparked discussions in academic forums and patent filings. Its low environmental persistence compared to bulkier amines further positions it as a candidate for eco-friendly industrial processes.

Synthetic routes to CAS No. 219736-10-4 often involve reductive amination of cyclopropyl ketones or ring-opening strategies, with yields optimized via modern techniques like flow chemistry. Analytical methods such as GC-MS and NMR spectroscopy confirm its high purity (>98%), a critical parameter for regulatory compliance in pharmaceuticals. Notably, the compound's boiling point (estimated 150–160°C) and logP value (~1.2) make it suitable for formulations requiring moderate hydrophobicity, a feature frequently queried in chemical databases.

From an SEO perspective, users frequently search for "1-cyclopropylpropan-1-amine suppliers," "CAS 219736-10-4 safety data," or "cyclopropylamine derivatives in drug design," reflecting commercial and research priorities. Addressing these queries, this compound's handling guidelines recommend inert atmosphere storage to prevent oxidation, while its compatibility with common solvents (e.g., ethanol, DCM) is documented in technical literature. Emerging applications in battery electrolytes and polyurethane catalysts further expand its market relevance, as noted in recent investor reports.

In conclusion, 1-cyclopropylpropan-1-amine exemplifies the intersection of structural innovation and practical utility. Its role in advancing precision medicine and sustainable industrial chemistry ensures continued academic and commercial interest. Future research may explore its enantioselective synthesis or hybrid materials, topics gaining traction in peer-reviewed journals and grant proposals.

• 54187-20-1(Bis(2-methylcyclopropyl)methanamine)
• 61888-94-6(Bicyclo[5.1.0]octan-8-amine)
• 1342230-69-6(2-(2-methylpropyl)cyclopropan-1-amine)
• 2248212-74-8((2R)-3-Cyclopropylbutan-2-amine)
• 777010-06-7(Bicyclo[5.1.0]octan-2-amine,(1R,2S,7S)-rel-)
• 195604-39-8((1S)-1-cyclopropylethanamine)
• 13375-29-6(Dicyclopropylmethanamine)
• 6240-96-6((1R)-1-cyclopropylethanamine)
• 388631-23-0(Cyclopropanamine,2-pentyl-, (1R,2R)-rel-)
• 1621-24-5(1-Cyclopropylethanamine)