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Cabozantinib
Venkatasai is a leading provider of pharmaceutical reference standards, specializing in the supply of high-purity Cabozantinib 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 Cabozantinib-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.
Cabozantinib
4-Fluoroaniline HCl Cabozantinib Impurity
Cabozantinib Quinol Impurity
Cabozantinib N-oxide
Cabozantinib Carboxylic Acid
Cabozantinib Hydroxy Impurity
Cabozantinib Dimer Impurity 1
Cabozantinib Des Fluoro Impurity
Cabozantinib Impurity 1
Cabozantinib Impurity 2
Cabozantinib Impurity 3
Cabozantinib Impurity 4
Cabozantinib Impurity 5
Cabozantinib Impurity 6
Cabozantinib 2-fluoro impurity
Cabozantinib 3-fluoro impurity
Cabozantinib Acid impurity
Cabozantinib Impurity 10
Cabozantinib Impurity 11
Cabozantinib Impurity 12
Cabozantinib Fumarate
Cabozantinib Dimer impurity
Cabozantinib Impurity 13
Cabozantinib Impurity 14
Cabozantinib Impurity 15
