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

Azilsartan Medoxomil Related Compounds

Stable Isotopes

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Azilsartan Medoxomil-D5 Stable Isotopes CS-T-100813 Not Available Enquire


API Standards

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Azilsartan Medoxomil API Standards CS-O-00914 863031-21-4 In Stock
Azilsartan Medoxomil Potassium API Standards CS-O-16101 863031-24-7 In Stock


Impurities

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Azilsartan medoxomil diazirin impurity Impurities CS-O-57997 Not Available Enquire
Azilsartan Medoxomil Dimer Impurity Impurities CS-O-40698 Not Available Enquire
Desethyl Azilsartan Medoxomil Impurities CS-T-73932 1417576-00-1 In Stock
N-Ethyl Azilsartan Medoxomil Impurities CS-T-73152 1417576-01-2 Enquire