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Clearsynth is a leading innovator in pharmaceutical reference standards, offering high-quality Reference Standards for Vinorelbine Ditartrate, including both pharmacopeial and non-pharmacopeial impurities, metabolites, stable isotope products, and nitrosamines (N-NO products). Our Vinorelbine Ditartrate 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 Vinorelbine Ditartrate-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.

Vinorelbine Ditartrate Related Compounds

API

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Vinorelbine Ditartrate API CS-O-02571 125317-39-7 In Stock


Impurity

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
3,6-Epoxy vinorelbine Impurity CS-O-56607 95377-57-4 Enquire
Vinorelbine EP Impurity E Impurity CS-EO-03941 23360-92-1 Enquire