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Orlistat
Venkatasai is a leading provider of pharmaceutical reference standards, specializing in the supply of high-purity Orlistat 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 Orlistat -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.
Orlistat
Orlistat USP Related Compound A
Orlistat USP Related Compound B
Orlistat USP Related Compound C
Orlistat USP Related Compound D
Orlistat USP Related Compound E
Orlistat Formyl Impurity
(R,S,S,S)-Orlistat
Orlistat Open Ring Epimer
N-Formyl-L-leucine Orlistat
Orlistat Dihydropyranone Impurity
Orlistat Delactone
(S,S,R,R)-Orlistat
Orlistat Tetradecyl Ester
Orlistat Open Ring Amide
Orlistat Impurity 1
Orlistat Impurity 2
Orlistat Impurity 3
Orlistat Impurity 4
Orlistat Impurity 5
Orlistat Impurity 6
Orlistat Impurity 7
Methyl Orlistat
N-Nitroso Orlistat
