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Clearsynth is a leading innovator in pharmaceutical reference standards, offering high-quality Reference Standards for Ruxolitinib Phosphate, including both pharmacopeial and non-pharmacopeial impurities, metabolites, stable isotope products, and nitrosamines (N-NO products). Our Ruxolitinib Phosphate impurity reference standards are invaluable for pharmaceutical research, supporting product development, ANDA and DMF submissions, quality control (QC), method validation, and stability studies. They also aid in identifying unknown impurities and assessing genotoxic potential.
Our Ruxolitinib Phosphate-related products undergo thorough characterization and are supplied with detailed Certificates of Analysis (COA) and analytical data that meet regulatory requirements. All supplied products are re-tested at regular intervals to ensure ongoing quality and compliance.

Ruxolitinib Phosphate Related Compounds

Impurity

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
(S)-Ruxolitinib Phosphate Impurity CS-EO-03841 2703484-89-1 Enquire
Ruxolitinib acid Phosphate salt Impurity CS-O-45234 2102675-40-9(Freebase ) Enquire
Ruxolitinib Phosphate Impurity CS-T-61212 1092939-17-7 In Stock


Secondary Standards

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Ruxolitinib Phosphate Secondary Standards CS-O-45655 1092939-17-7 In Stock