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Clomipramine
Venkatasai is a leading provider of pharmaceutical reference standards, specializing in the supply of high-purity Clomipramine 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 Clomipramine-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.
Clomipramine
Clomipramine Hydrochloride
Clomipramine Hydrochloride EP Impurity A
Clomipramine Hydrochloride EP Impurity B
Clomipramine Hydrochloride EP Impurity C
Clomipramine EP Impurity D (HCl)
Clomipramine Hydrochloride EP Impurity E
Clomipramine Hydrochloride EP Impurity F
Clomipramine Hydrochloride EP Impurity G
Clomipramine EP Impurity A (2HCl)
Didesmethyl Clomipramine
8-Hydroxy Desmethyl Clomipramine
8-Hydroxy Clomipramine
Clomipramine N-Oxide
N-Desmethyl Clomipramine HCl
Clomipramine Hydroxy impurity (photho degradation)
N-Nitroso Desmethyl Clomipramine
Clomipramine Impurity 1
Clomipramine Impurity 2
Clomipramine Impurity 3
Clomipramine Impurity 4
Clomipramine Impurity 5
Clomipramine Impurity 6
Clomipramine Impurity 7
Clomipramine Impurity 8
Clomipramine Impurity 9
Clomipramine Impurity 10
Clomipramine Impurity 11
Clomipramine Impurity 12
Clomipramine Impurity 13
Clomipramine Impurity 14
Clomipramine Impurity 15
