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

Clavulanate Potassium Related Compounds

API Standards

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Clavulanate potassium API Standards CS-O-06232 61177-45-5 In Stock


Impurities

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Clavulanic acid EP impurity B Impurities CS-T-06997 96681-85-5 Enquire
Sterile Clavulanate Potassium+Amoxicillin Impurities CS-O-15494 61177-45-5 & 26787-78-0 Enquire