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Capecitabine
Venkatasai is a leading provider of pharmaceutical reference standards, specializing in the supply of high-purity Capecitabine 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 Capecitabine-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.
Capecitabine
Capecitabine Hydrochloride
Capecitabine EP Impurity A
Capecitabine EP Impurity A Hydrochloride
Capecitabine EP Impurity A Hydrobromide
Capecitabine EP Impurity B
Capecitabine EP Impurity C
Capecitabine EP Impurity C Hydrochloride
Capecitabine EP Impurity D
Capecitabine EP Impurity E
Capecitabine EP Impurity F
Capecitabine EP Impurity G
Capecitabine EP Impurity M
Capecitabine 2-O-BDR Impurity (USP)
Capecitabine 3-O-BDR Impurity (USP)
Capecitabine α-Isomer
Capecitabine α-Isomer Diacetyl Impurity
Tetrahydrouridine
3’-(5’-Deoxy-Alfa-D-ribofuranoyl) Capecitabine
Capecitabine Isomers
Capecitabine Impurity 1
Capecitabine Impurity 2
Capecitabine Impurity 3 (Defluoro Capecitabine)
Capecitabine Impurity 4
Capecitabine Impurity 5
Capecitabine Impurity 6
Capecitabine Impurity 7
Capecitabine Impurity 8
Capecitabine Impurity 9
