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Sibutramine
Venkatasai is a leading provider of pharmaceutical reference standards, specializing in the supply of high-purity Sibutramine 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 Sibutramine-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.
Sibutramine
N-Desmethyl Sibutramine
N,N-Didesmethyl Sibutramine
N-Formyl N,N-Didesmethyl Sibutramine
Benzyl Sibutramine
Chloro-Sibutramine HCl
Homo Sibutramine
Sibutramine N-Oxide
Sibutramine Carbamic Acid Impurity 1
(N,N-Didemethyl)-1-Hydroxy-Sibutramine
Sibutramine Impurity E
Sibutramine Impurity F
Sibutramine Impurity H
Sibutramine Impurity I
Sibutramine Impurity J
Sibutramine Hydrochloride Related Compound A
Sibutramine Hydrochloride Related Compound B
Sibutramine Hydrochloride Related Compound C
Sibutramine Hydrochloride Related Compound D
Sibutramine Related Compound 1
Sibutramine Impurity 1
Sibutramine Impurity 2
Sibutramine Impurity 3
Sibutramine Hydrochloride Monohydrate
