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Dapoxetine
Venkatasai is a leading provider of pharmaceutical reference standards, specializing in the supply of high-purity Dapoxetine 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 Dapoxetine -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.
Dapoxetine HCl
Dapoxetine Hydroxy Impurity
N-Didesmethyl Dapoxetine Hydrochloride
Dapoxetine N-Oxide
Dapoxetine Impurity A
Dapoxetine HCl [R-Isomer]
![Picture of Dapoxetine HCl [R-Isomer]](https://venkatasailifesciences.com/content/images/thumbs/0035940_dapoxetine-hcl-r-isomer_350.png "Show details for Dapoxetine HCl [R-Isomer]")
Dapoxetine N-Oxide Hydrochloride
rac N-demethyl dapoxetine
N-Desmethyl Dapoxetine Hydrochloride
Dapoxetine Impurity 1
Dapoxetine Impurity 2
Dapoxetine
Dapoxetine impurity 3
Dapoxetine-d6 Hydrochloride
Dapoxetine Impurity B
Racemic Dapoxetine Hydrochloride
Dapoxetine Impurity 4
Dapoxetine Impurity 5
