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

Doxifluridine Related Compounds

Stable Isotopes

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Doxifluridine-13C5 Stable Isotopes CS-T-103652 3094-09-5(unlabelled) Enquire


API Standards

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Doxifluridine API Standards CS-O-07516 3094-09-5 In Stock


Impurities

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Doxifluridine Related Compound A Impurities CS-O-05553 Not Available Enquire