Gliclazide EP Impurity F

For pharmaceutical manufacturers striving for uncompromising purity, Manasa Life Sciences offers a high-specification Gliclazide EP Impurity F (CAS: 1076198-18-9), the definitive analytical standard for detecting and quantifying process-related impurities. Chemically identified as N-[[(Hexahydrocyclopenta[c]pyrrol-2(1H)-yl)amino]carbonyl]-2-methylbenzenesulfonamide, this material maintains a molecular formula of C₁₅H₂₁N₃O₃S and a molecular weight of 323.41 g/mol. This critical reference material is indispensable for laboratories performing impurity profiling in alignment with EP and USP regulatory standards. As a trusted manufacturer and supplier, we utilize advanced instrumentationincluding HPLC, LC-MS, NMR, and IRto validate the identity and purity of this complex compound. Our commitment to GMP and GDP excellence ensures that every sample is handled with the precision required for high-stakes analytical testing, supporting developers in meeting USFDA and other international regulatory filings. By integrating our Gliclazide EP Impurity F into your quality management systems, you gain access to a reliable, well-characterized reference material supported by a full COA and MSDS, providing the technical documentation necessary to identify and control potential degradation or process byproducts.