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Diosmin
Venkatasai is a leading provider of pharmaceutical reference standards, specializing in the supply of high-purity Diosmin 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 Diosmin-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.
Diosmin
Diosmin EP Impurity A
Diosmin EP Impurity B
Diosmin EP Impurity C
Diosmin EP Impurity D
Diosmin EP Impurity E
Diosmin EP Impurity F
Diosmin EP Impurity G
Didymin
Diosmin-7-O-beta-D-Glucoside
Diosmin Impurity 1
Diosmin Impurity 2
Diosmetin 3-O-b-D-Glucuronide
Diosmetin-7-O-glucuronide
