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Selexipag
Venkatasai is a leading provider of pharmaceutical reference standards, specializing in the supply of high-purity Selexipag reference materials. Our portfolio includes both pharmacopeial and non-pharmacopeial impurities, metabolites, stable isotope-labeled compounds, and nitrosamine derivatives (N-NO products). These reference standards play a crucial role in pharmaceutical R&D, aiding in formulation development, ANDA/DMF submissions, quality control, method validation, stability studies, and impurity profiling—including the identification and assessment of potentially genotoxic impurities.
Each Selexipag-related product is rigorously characterized and delivered with a detailed Certificate of Analysis (COA) and comprehensive analytical data to ensure regulatory compliance. Upon request, we also offer EP/USP traceable standards. To maintain the highest quality standards, all materials are subject to periodic re-testing and continuous quality monitoring.
Selexipag
Selexipag Acid
Selexipag Impurity A
Selexipag Impurity B
Selexipag Impurity C
Selexipag Impurity D
Selexipag Methyl Ester Impurity
Selexipag acyl β-D-Glucuronide
Selexipag Impurity 1
Selexipag Impurity 2
Selexipag Impurity 4
Selexipag Impurity 5
Selexipag Impurity 6
Selexipag Impurity 9
Selexipag Glycine Adduct 13C2,15N
Selexipag Glycine Adduct
