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

Anagliptin Related Compounds

Stable Isotopes

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Anagliptin-D6 Stable Isotopes CS-EO-02420 739366-20-2 (unlabeled) Enquire
Anagliptin-d7 Stable Isotopes CS-O-11889 739366-20-2(Unlabeled) In Stock


API Standards

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Anagliptin API Standards CS-O-13604 739366-20-2 In Stock


Impurities

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Anagliptin impurity F Impurities CS-AQ-00226 Not Available Enquire
Anagliptin impurity G Impurities CS-AQ-00227 1263061-14-8 Enquire