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Understanding the Chemical Properties and Synthesis of CAS 42142-52-9

For chemists and formulators, a deep understanding of chemical intermediates is key to successful product development. 3-Hydroxy-N-methyl-3-phenyl-propylamine (CAS 42142-52-9) stands out as a versatile aromatic amino alcohol with significant utility in various chemical processes. Its molecular formula, C10H15NO, and a molecular weight of approximately 165.23 g/mol, hint at its structural complexity and reactivity.

The reported physical properties indicate it typically presents as an off-white solid, with a melting point around 64°C. Its boiling point is noted at 170°C at 31 mmHg, suggesting reasonable thermal stability for processing. This compound is also recognized for its role as an initiator in radical addition reactions with tetrahalomethanes, a testament to its chemical functionality. For those seeking to purchase this compound, understanding these properties is crucial for appropriate handling and application.

The synthesis of 3-Hydroxy-N-methyl-3-phenyl-propylamine often involves multi-step processes, with established routes typically starting from propiophenone derivatives or epoxy styrene compounds. These synthetic pathways are vital for manufacturers aiming to produce high-purity material. For researchers and buyers, knowing the synthesis methods can also shed light on potential impurities and quality variations. As a leading chemical supplier, we focus on optimized synthesis and purification techniques to deliver a consistently high-grade product.

The compound is also identified as an impurity in Fluoxetine and an intermediate in Fluoxetine Hydrochloride synthesis. This dual role underscores its importance in the pharmaceutical sector. If your research or manufacturing requires this specific chemical intermediate, engaging with a reputable manufacturer is essential. We are a dedicated supplier focused on providing reliable access to CAS 42142-52-9, offering competitive pricing and bulk purchase options to meet your project needs.

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