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Nelarabine
Venkatasai is a leading provider of pharmaceutical reference standards, specializing in the supply of high-purity Nelarabine 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 Nelarabine-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.
Nelarabine
Nelarabine Stage-I Impurity
Nelarabine Alpha Isomer
Nelarabine Regio Isomer
6-O-Methylguanine
Nelarabine Diamine Impurity
Nelarabine Impurity 1
Nelarabine Impurity 2
Nelarabine Impurity 3
Nelarabine Impurity 4
Nelarabine Impurity 5
Nelarabine Impurity 6
Nelarabine Impurity 7
Nelarabine Impurity 8
Nelarabine Impurity 9
Nelarabine Impurity 10
Nelarabine Impurity 11
Nelarabine Impurity 12
Nelarabine Impurity 13
Nelarabine Impurity 14
Nelarabine Impurity 15
Nelarabine Impurity 16
Nelarabine Impurity 17
