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Vilanterol
Venkatasai is a leading provider of pharmaceutical reference standards, specializing in the supply of high-purity Vilanterol 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 Vilanterol-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.
Vilanterol
Vilanterol Trifenatate
Vilanterol Impurity 1
Vilanterol Impurity I
Vilanterol Impurity 3
Vilanterol Impurity 4
Vilanterol Impurity 5
Vilanterol Impurity 6
Vilanterol Impurity 7
Vilanterol Impurity 8
Vilanterol Impurity 9
Vilanterol Impurity 10
Vilanterol Impurity 11
Vilanterol S-Isomer impurity
Vilanterol Impurity 12
Vilanterol Impurity 13
Vilanterol Impurity 14
Vilanterol Impurity 15
Vilanterol Impurity 16
Vilanterol Nitroso Impurity 1
Vilanterol Nitroso Impurity 2
