Losartan Impurity 55 CAS 212316-86-4

Purity 97%+In StockPharmacopoeial Impurity Standards
CAS No.212316-86-4
Molecular FormulaC44H44Cl2N12O
Molecular WeightN/A
CategoryPharmacopoeial Impurity Standards / EP Impurities
AvailabilityIn Stock

Chemical Structure

Losartan Impurity 55 CAS 212316-86-4 chemical structure

Description

CATO supplies Losartan Impurity 55 (CAS 212316-86-4), a pharmacopoeial impurity reference standard (molecular formula C44H44Cl2N12OK, MW 866.92 g/mol) used for the identification and quantification of trace impurities in APIs.

Losartan Impurity 55 (C44H44Cl2N12OK) contains a salt form, a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, chlorine 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.

CATO manufactures Losartan Impurity 55 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.

Physical & Chemical Properties

Molecular FormulaC44H44Cl2N12O K
Molecular Weight866.92 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)28.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2017
Halogen ContentCl-containing
Nitrogen Atoms12

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