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Ambrisentan
Venkatasai is a leading provider of pharmaceutical reference standards, specializing in the supply of high-purity Ambrisentan 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 Ambrisentan-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.
Ambrisentan
Ambrisentan (R)-Isomer
Ambrisentan 4-Hydroxymethyl Analog
Ambrisentan 4-Hydroxymethyl Analog Racemate
Ambrisentan Racemate
Ambrisentan Ethyl Ester
Ambrisentan Ethyl Ester Racemate
Ambrisentan Methyl Ester
Ambrisentan Methyl Ester Racemate
Ambrisentan Vinyloxy Impurity
Ambrisentan Hydroxy Acid Impurity (R-Isomer)
Ambrisentan Impurity E
Ambrisentan Hydroxy Acid Impurity (S-isomer)
Ambrisentan Hydroxyester Impurity
Ambrisentan pyrimidine Ester Impurity
Ambrisentan N-Oxide
Ambrisentan Epoxide
Ambrisentan Impurity 1
Ambrisentan Impurity 2
Ambrisentan D3
Rac O-Demethyl Ambrisentan
