Iopamidol Impurity 52 CAS 60166-91-8

Purity 97%+In StockPharmacopoeial Impurity Standards
CAS No.60166-91-8
Molecular FormulaC13H8Cl2I3NO5
Molecular Weight709.83 g/mol
CategoryPharmacopoeial Impurity Standards / EP Impurities
AvailabilityIn Stock

Chemical Structure

Iopamidol Impurity 52 CAS 60166-91-8 chemical structure

Description

CATO manufactures Iopamidol Impurity 52 under ISO 17034:2016 accreditation with dual CNAS and ANAB accreditation. Each batch is characterized by orthogonal methods and supplied with a full Certificate of Analysis (COA), ensuring metrological traceability.

CATO supplies Iopamidol Impurity 52 (CAS 60166-91-8), a pharmacopoeial impurity reference standard (molecular formula C13H8Cl2I3NO5, MW 709.83 g/mol) used for the identification and quantification of trace impurities in APIs.

The molecular framework of Iopamidol Impurity 52 (C13H8Cl2I3NO5) is characterized by a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, chlorine/iodine substitution. In reversed-phase chromatography, its retention is governed primarily by the protonation state of its nitrogen-containing groups, which provides a practical basis for HPLC-UV/DAD or LC-MS method development. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

This reference standard supports related-substances testing and method development in line with ICH Q3A/Q3B guidance on impurity control, and is suitable for system suitability testing and forced-degradation studies.

Physical & Chemical Properties

Molecular FormulaC13H8Cl2I3NO5
Molecular Weight709.83 g/mol
Purity97%+
StorageStore in a cool place (≤25°C), protect from light, keep sealed and dry
Solubility (reference)Soluble in methanol, acetonitrile, DMSO, water (slightly soluble)
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Hygroscopic; reseal immediately after opening; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)8.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1974
Halogen ContentCl/I-containing
Nitrogen Atoms1

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