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

Gadoteridol Related Compounds

API Standards

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Gadoteridol API Standards CS-T-55155 120066-54-8 Enquire
Gadoteridol Impurity 2 API Standards CS-T-21342 60239-18-1 In Stock


Impurities

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Butrol triammonia salt Impurities CS-O-35818 151852-61-8 (Free base) Enquire
Des(2-Hydroxypropyl) Gadoteridol Impurities CS-T-52183 112188-16-6 Enquire
Desgadolinium Gadoteridol Impurities CS-T-15969 120041-08-9 Enquire
DOTA Caclim Salt Impurities CS-O-57451 60239-18-1(Freebase) Enquire
Gadoteridol Impurity F Impurities CS-O-53359 Not Available Enquire
Gadoteridol Related Compound C Impurities CS-T-38493 220182-19-4 Enquire