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Dienogest
Venkatasai is a leading provider of pharmaceutical reference standards, specializing in the supply of high-purity Dienogest 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 Dienogest-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.
Dienogest
Dienogest EP Impurity A
Dienogest EP Impurity B
Dienogest EP Impurity C
Dienogest EP Impurity D
Dienogest EP Impurity G
Dienogest EP Impurity H
Dienogest EP Impurity I
Dienogest EP Impurity J
Dienogest EP Impurity L
Dienogest EP Impurity M
Dienogest EP Impurity E
Dienogest EP Impurity F
Dienogest EP Impurity K
6-beta-Hydroxy Dienogest
3,3-Dimethoxyestra-5(10),9(11)-dien-17-one
Estra-5(10),9(11)-diene-3,17-dione
Estra-5(10),9(11)-diene-3,17-dione Cyclic 3,17-Bis(1,2-ethanediyl acetal)
17-epi-Dienogest
Seco-Dienogest
Dienogest Impurity 1
Dienogest Impurity 4
Dienogest Impurity 5
