Clioquinol EP Impurity C

Review on analytical studies of some pharmaceutical compounds containing heterocyclic rings: brinzolamide, timolol maleate, flumethasone pivalate, and clioquinol
Asmaa A. Mandour, Nada Nabil, Hala E. Zaazaa & Mohamed Abdelkawy
Future Journal of Pharmaceutical Sciences volume 6, Article number: 52 (2020)
 
Determining the Antifungal Agent Clioquinol by HPLC, the Not So Pure Preparation: A Laboratory-Based Case Study for an Instrumental Analytical Chemistry Course
Peter M. Schaber* and Geoffrey Hobika
J. Chem. Educ. 2018, 95, 3, 445–450
 
Spectrophotometric Determination of Clioquinol and Diodoquin in Pharmaceutical Preparations Using Uranyl Acetate as a Chromogenic Agent
U. Saha, A. K. Sen and T. K. Das
Analyst, november 1988, VOL. 113

Clioquinol EP Impurity C is chemically 5,7-Diiodoquinolin-8-ol. It is also known as Clioquinol BP Impurity C ; Iodoquinol (USP). Clioquinol EP Impurity C is supplied with detailed characterization data compliant with regulatory guideline. Clioquinol EP Impurity C can be used for the analytical method development, method validation (AMV), Quality Controlled (QC) application for Abbreviated New Drug Application (ANDA) or during commercial production of Clioquinol.

The product can be used as reference standards and further traceability against pharmacopeial standards (USP or EP) can be provided based on feasibility. SynZeal products are for analytical purpose only and not for human use.