Bimatoprost API, scientifically identified by its CAS number 155206-00-1 and molecular formula C25H37NO4, is a complex organic molecule characterized by its unique prostaglandin-like structure. Its molecular weight of 415.57 g/mol and its typical appearance as a white or off-white crystalline powder are key physical attributes that manufacturers rely on. The solubility profile of Bimatoprost, being practically insoluble in water but soluble in organic solvents like ethanol and methanol, influences its formulation processes.

The manufacturing of high-quality Bimatoprost API involves meticulous processes to ensure purity and consistency. Companies adhere to stringent Good Manufacturing Practices (GMP) to guarantee that each batch meets pharmaceutical and cosmetic grade standards. This includes rigorous in-process controls and final product testing for parameters such as assay (typically 99% by HPLC), related substances, water content, and residual solvents. Compliance with pharmacopoeial standards like USP and BP is essential for its intended therapeutic and cosmetic applications.

The production process often involves multi-step synthesis, purification through chromatography, and controlled crystallization to achieve the desired purity. Packaging and storage are also critical to maintaining the stability of Bimatoprost API. It is typically stored in tightly closed, light-resistant containers at cool temperatures to preserve its efficacy over its shelf life. For manufacturers, partnering with suppliers who can provide comprehensive documentation, including detailed technical specifications, COAs, and MSDS, is fundamental to ensuring the integrity of their final products derived from Bimatoprost API.