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Crisaborole
Venkatasai is a leading provider of pharmaceutical reference standards, specializing in the supply of high-purity Crisaborole 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 Crisaborole-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.
Crisaborole
Crisaborole m-Isomer
Crisaborole o-Isomer
Crisaborole Impurity A
Crisaborole Impurity B
Crisaborole Impurity D
Crisaborole Impurity C
Crisaborole Acid Impurity
Crisaborole Stage-I Impurity
Crisaborole Dimer Impurity
Crisaborole Impurity 1
Crisaborole Impurity 2
Crisaborole Impurity 3
Crisaborole Impurity 4
Crisaborole Impurity 5
Crisaborole Impurity 6
Crisaborole Impurity 7
Crisaborole Impurity 8
