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Phenylpropionamide

Updated: 2026-08-03

Overview

Phenylpropionamide is an organic compound derived from phenylpropionic acid, primarily used as an intermediate in pharmaceutical synthesis. Its molecular structure combines a benzene ring with an amide group, making it versatile for further chemical modifications. The compound is valued in B2B markets for its role in producing active pharmaceutical ingredients (APIs) and specialty chemicals. Industrial production typically involves amidation reactions of phenylpropionic acid derivatives under controlled conditions. Manufacturers often supply it in bulk quantities with varying purity grades (e.g., 98%-99.5%), tailored to end-use requirements.

Physical and Chemical Properties

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Phenylpropionamide exhibits stable physical properties under standard conditions. Its crystalline form ensures ease of handling in industrial settings, while its solubility profile allows flexibility in solvent selection for reactions. The melting point range (130-135°C) indicates suitability for processes requiring moderate heat resistance. Chemically, the amide group lends reactivity for condensation or hydrolysis reactions, whereas the phenyl ring contributes to lipophilicity—a critical factor in drug design. Analytical methods like HPLC and NMR are commonly employed for quality verification due to the compound's pharmaceutical relevance.

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Main Applications

The primary use of phenylpropionamide lies in synthesizing analgesics, anticonvulsants, and other CNS-targeting drugs. It serves as a building block for compounds such as felbamate, an antiepileptic medication. Additionally, agrochemical manufacturers utilize it to create crop protection agents with enhanced stability. In research, this amide is a precursor for fluorescent probes and polymer modifiers. Its compatibility with peptide coupling reagents expands utility in bioconjugation applications, meeting demand from biotech and material science sectors.

Safety and Storage

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While phenylpropionamide is not classified as highly hazardous, proper safety measures are essential. Dust formation during handling may irritate respiratory tracts, necessitating NIOSH-approved masks and ventilation. Skin contact should be minimized using nitrile gloves and lab coats. Storage recommendations include airtight containers in temperature-controlled environments (15-25°C) to prevent moisture absorption or degradation. Incompatible with strong oxidizers, it requires segregation from acids and bases in chemical warehouses. SDS documentation must be accessible per OSHA regulations.

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B2B Procurement Guide

Buyers should prioritize suppliers with documented cGMP compliance for pharmaceutical-grade material. Key evaluation criteria include batch-to-batch consistency (verified via COA), residual solvent levels, and heavy metal content. Spot purchases typically range from $50-$200/kg depending on volume and purity. Logistics considerations: Opt for manufacturers offering hazmat-certified shipping for international orders. Sample testing through third-party labs is advisable before large-scale procurement. Long-term contracts often include MOQ discounts and stability data support.

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