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

Cangliflozin Related Compounds

Impurities

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Cangliflozin Impurity 2 Impurities CS-T-93363 1951467-28-9 Enquire
Cangliflozin Impurity 5 Impurities CS-EO-00784 Not Available Enquire
Cangliflozin Impurity 6 Impurities CS-EO-00289 2161394-96-1 Enquire
Cangliflozin Impurity 7 Impurities CS-O-34449 Not Available Enquire
Cangliflozin-3-Regio isomer Impurities CS-O-34450 Not Available Enquire