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Bosutinib
Venkatasai is a leading provider of pharmaceutical reference standards, specializing in the supply of high-purity Bosutinib 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 Bosutinib-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.
Bosutinib
Bosutinib Didesmethyl Impurity
Bosutinib Desmethyl Impurity
N-Desmethyl bosutinib
Bosutinib Dimer Impurity
Bosutinib Impurity I
Bosutinib Impurity II
Bosutinib Des NMP Impurity
3-Allyloxy-4-methoxynitrobenzene
2-Methoxy-5-nitrophenol
2,4-Dichloro-5-methoxyaniline
Bosutinib Oxydechlorinated Impurity
Bosutinib N-oxide Bosutinib
Bosutinib Propoxy Dimer Impurity
2-Methoxy-5-nitrophenol Sodium salt
2-Methoxy-5-nitrophenol Potassium salt
2,4-Dichloro-5-methoxyaniline Hydrochloride
Bosutinib Regio Isomer Impurity
Bosutinib Impurity 1
Bosutinib Impurity 2
Bosutinib Impurity 3
Bosutinib Impurity 4
Bosutinib Impurity 5
Bosutinib Impurity 6
Bosutinib Impurity 7
Bosutinib Impurity 8
Bosutinib Monohydrate
