Palmitoylethanolamide

Product Overview

Palmitoylethanolamide, commonly abbreviated as PEA, is a naturally occurring fatty acid amide that belongs to the class of nuclear factor agonists. Our premium grade material is synthesized under strict Good Manufacturing Practices to ensure consistency and safety for downstream formulation. This compound is widely recognized in the scientific community for its role as an endogenous lipid mediator, contributing to cellular homeostasis and comfort support within various biological systems. As a versatile ingredient, it bridges the gap between cosmetic science and nutraceutical innovation, providing formulators with a robust solution for high-performance products.

Chemical Properties And Structure

Chemically identified as N-(2-hydroxyethyl)hexadecanamide, this molecule features a stable amide bond linked to a palmitic acid chain. The structural integrity of our supply ensures high melting point characteristics suitable for diverse processing conditions. With a molecular formula of C18H37NO2 and a molecular weight of approximately 299.49 g/mol, the substance exhibits low volatility and excellent thermal stability. These physical attributes make it an ideal candidate for incorporation into solid dosage forms, topical creams, and personal care emulsions without compromising the final product profile.

Industrial Applications

The utility of Palmitoylethanolamide extends across multiple sectors, primarily focusing on health and personal care. In the nutraceutical industry, it is utilized as a key active ingredient designed to support the body's natural response to everyday stress and discomfort. In cosmetic formulations, it functions as a nonionic surface active agent that enhances the texture and distribution of shampoos, soaps, and lotions. Its ability to integrate seamlessly into lipid phases allows for improved skin feel and product stability. Manufacturers seeking a reliable source for functional ingredients will find this material meets rigorous performance benchmarks for both efficacy and safety.

Quality Assurance And Specifications

We maintain a comprehensive quality control protocol to guarantee that every batch meets international standards. Each lot undergoes extensive testing using High-Performance Liquid Chromatography (HPLC) to verify purity levels exceeding 98 percent. Additional analyses include loss on drying, residue on ignition, and heavy metal screening to ensure consumer safety. Our facility adheres to strict storage guidelines, keeping the material in a cool, ventilated environment to preserve potency. Customers receive a full Certificate of Analysis with every shipment, providing transparency and traceability from synthesis to delivery.

Key Advantages

• High purity assay suitable for sensitive formulations
• Excellent thermal stability for diverse manufacturing processes
• Verified low heavy metal content for safety compliance
• Consistent particle size for uniform dispersion
• Supported by comprehensive technical documentation

Technical Specifications