Dexlansoprazole Impurity 7 CAS 1781244-56-1

Purity 97%+In StockPharmacopoeial Impurity Standards
CAS No.1781244-56-1
Molecular FormulaC23H16F3N5OS
Molecular Weight467.47 g/mol
CategoryPharmacopoeial Impurity Standards / EP Impurities
AvailabilityIn Stock

Chemical Structure

Dexlansoprazole Impurity 7 CAS 1781244-56-1 chemical structure

Description

CATO manufactures Dexlansoprazole Impurity 7 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 Dexlansoprazole Impurity 7 (CAS 1781244-56-1), a pharmacopoeial impurity reference standard (molecular formula C23H16F3N5OS, MW 467.47 g/mol) used for the identification and quantification of trace impurities in APIs.

Dexlansoprazole Impurity 7 (C23H16F3N5OS) contains a steroid core, an amide group, sulfur-containing functionality, a hydroxyl group, an ether linkage, fluorine substitution. Halogen substitution raises its density and boiling point; these physicochemical properties determine the optimal preparation and storage of its standard solutions. 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 FormulaC23H16F3N5OS
Molecular Weight467.47 g/mol
Purity97%+
StorageStore at room temperature, protect from light
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)17.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1994
Halogen ContentF-containing
Nitrogen Atoms5
Sulfur Atoms1

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