The Chemistry and Quality of Pharmaceutical Grade Iloprost
NINGBO INNO PHARMCHEM CO.,LTD. specializes in the synthesis and supply of high-quality pharmaceutical chemicals, with Iloprost being a prime example. The precision involved in producing pharmaceutical-grade Iloprost is paramount, given its critical role in treating severe medical conditions. This article explores the chemistry behind Iloprost and the stringent quality controls that govern its production.
Iloprost, with the CAS number 78919-13-8, is a complex organic molecule belonging to the prostacyclin analogue class. Its chemical formula, C22H32O4, and a molecular weight of approximately 360.49 g/mol, describe a molecule carefully engineered to mimic the biological actions of prostacyclin. As a synthetic prostacyclin analogue, its structure is optimized for therapeutic efficacy and stability, distinguishing it from natural compounds.
The production of pharmaceutical-grade Iloprost involves multi-step synthesis, demanding advanced chemical expertise and state-of-the-art facilities. Achieving a high purity level, often specified as greater than 98% or even 99%, is non-negotiable. This purity is typically verified through rigorous analytical techniques such as High-Performance Liquid Chromatography (HPLC) and Gas Chromatography (GC). NINGBO INNO PHARMCHEM CO.,LTD. ensures that its Iloprost GMP USP grade material meets these exacting standards.
Quality assurance extends beyond purity to include aspects like appearance, solubility, and the absence of harmful impurities. Iloprost is generally described as a white or off-white solid powder, and its solubility characteristics in various solvents are well-defined. These physical and chemical properties are critical for its formulation into stable and effective drug products. The role of NINGBO INNO PHARMCHEM CO.,LTD. as a reliable Iloprost manufacturer ensures that these parameters are consistently met.
For pharmaceutical developers and researchers, sourcing pharmaceutical raw material Iloprost from certified suppliers is a fundamental requirement. It guarantees that the active ingredient will perform as expected in clinical trials and ultimately in patient treatments. The availability of such materials at competitive Iloprost price points from trusted Iloprost suppliers facilitates the entire drug development pipeline.
In conclusion, the meticulous synthesis and stringent quality control applied to Iloprost highlight its importance as a pharmaceutical chemical. NINGBO INNO PHARMCHEM CO.,LTD. is committed to upholding these high standards, providing the global healthcare industry with the essential building blocks for advanced medical therapies and contributing to better patient outcomes worldwide.
Perspectives & Insights
Data Seeker X
“Quality assurance extends beyond purity to include aspects like appearance, solubility, and the absence of harmful impurities.”
Chem Reader AI
“Iloprost is generally described as a white or off-white solid powder, and its solubility characteristics in various solvents are well-defined.”
Agile Vision 2025
“These physical and chemical properties are critical for its formulation into stable and effective drug products.”