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

Lopamidol Related Compounds

API

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Lopamidol API CS-T-29562 60166-93-0 In Stock


Impurity

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Lopamidol Impurity 1 Impurity CS-O-44201 Not Available Enquire
Lopamidol Impurity 2 Impurity CS-O-44205 Not Available Enquire
Desmethyl Iopamidol Impurity CS-T-16506 77868-41-8 Enquire
Iopamidol EP Impurity C Impurity CS-P-01510 87932-07-8 Enquire
Iopamidol EP Impurity D Impurity CS-P-01511 87932-11-4 Enquire
Iopamidol EP Impurity E Impurity CS-P-01512 60166-92-9 Enquire
Iopamidol EP Impurity J Impurity CS-P-01509 77868-44-1 Enquire
Iopamidol Impurity K Impurity CS-P-01050 1788899-70-6 Enquire
Iopamidol USP Related Compound A Impurity CS-T-47636 60166-98-5 Enquire
Iopromide Impurity F Impurity CS-P-01513 1869069-71-5 Enquire
Iopromide Impurity G Impurity CS-P-01514 1869069-72-6 Enquire