Sevoflurane stands out for its minimal metabolism in the body. This characteristic reduces the risk of producing harmful metabolites, contributing to the overall safety profile of the anesthetic. The ability to undergo minimal biotransformation enhances the predictability of its effects.
After synthesis, the crude API needs to be purified to eliminate impurities and obtain the desired purity level, often 98% or higher. Common purification techniques include recrystallization, distillation, chromatography, and membrane filtration. Each technique has its advantages and is selected based on the specific characteristics of the API. The purification process is critical as impurities can significantly impact the safety and efficacy of the final pharmaceutical product.
pharma api production process