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

Clodronate Related Compounds

Stable Isotopes

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Clodronate disodium salt 13C Stable Isotopes CS-CX-00247 138349-86-7 Enquire


API Standards

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Clodronic Acid API Standards CS-P-00903 10596-23-3 In Stock


Impurities

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Clodronate EP Impurity D Impurities CS-P-01253 87591-00-2 Enquire
Disodium Clodronate Tetrahydrate Impurities CS-O-04095 88416-50-6 In Stock