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

Clioquinol Related Compounds

API

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Clioquinol API CS-T-13125 130-26-7 In Stock


Impurity

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
5-Chloro-8-hydroxyquinoline Impurity CS-O-06307 130-16-5 In Stock
Clioquinol EP Impurity C Impurity CS-T-29541 83-73-8 In Stock


Intermediate

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
5,7-Dichloro-8-hydroxyquinoline Intermediate CS-O-06308 773-76-2 In Stock