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Ruxolitinib
Venkatasai is a leading provider of pharmaceutical reference standards, specializing in the supply of high-purity Ruxolitinib 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 Ruxolitinib-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.
Ruxolitinib
Ruxolitinib Phosphate
Ruxolitinib Diamine Impurity
Ruxolitinib Amide Impurity
Ruxolitinib Lactone Impurity
Ruxolitinib Hydroxy Impurity
Ruxolitinib SEM-Sulfonyl Impurity
Ruxolitinib M18 Metabolite
Ruxolitinib Acrylo pyrimidine Impurity
Ruxolitinib N-Oxide Impurity 1
Ruxolitinib N-Oxide Impurity 2
Ruxolitinib Impurity 1
Ruxolitinib Amide
Ruxolitinib Impurity 3
(S)-Ruxolitinib Phosphate
Ruxolitinib Impurity 5
Ruxolitinib acid amine impurity
Ruxolitinib Impurity 7
Ruxolitinib SEM tartaric acid S-isomer
Ruxolitinib Impurity 8
Ruxolitinib Impurity 9
Ruxolitinib Methyl Hydroxy
(S)-Ruxolitinib
Ruxolitinib Carboxylic acid
Ruxolitinib SEM Chloro pyrimidine
Ruxolitinib acid impurity
RUXOLUTINIB SEM-Cl impurity
Ruxolitinib Hydroxy Pyrimidine Impurity
Ruxolitinib Hemifumarate
