Cloransulam-Methyl Impurity 10 CAS CATO-C4X-317010

Purity ≥95%In StockPharmacopoeial Impurity Standards
CAS No.CATO-C4X-317010
Molecular FormulaC15H12Cl2FN5O5S
Molecular Weight464.26 g/mol
CategoryPharmacopoeial Impurity Standards / EP Impurities
AvailabilityIn Stock

Chemical Structure

Cloransulam-Methyl Impurity 10 CAS CATO-C4X-317010 chemical structure

Description

CATO manufactures Cloransulam-Methyl Impurity 10 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 Cloransulam-Methyl Impurity 10 (CAS CATO-C4X-317010), a pharmacopoeial impurity reference standard (molecular formula C15H12Cl2FN5O5S, MW 464.26 g/mol) used for the identification and quantification of trace impurities in APIs.

The molecular framework of Cloransulam-Methyl Impurity 10 (C15H12Cl2FN5O5S) is characterized by a flavonoid core, an amide group, a sulfone group, a hydroxyl group, an ether linkage, fluorine/chlorine 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. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

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 FormulaC15H12Cl2FN5O5S
Molecular Weight464.26 g/mol
Purity≥95%
StorageStore in a cool place (≤25°C), protect from light, keep sealed and dry
Solubility (reference)Soluble in DMSO, DMF, methanol
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)11.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
Halogen ContentF/Cl-containing
Nitrogen Atoms5
Sulfur Atoms1

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