Cefpirome Impurity 37 CAS CATO-C4X-120737

Purity >90%In StockPharmacopoeial Impurity Standards
CAS No.CATO-C4X-120737
Molecular FormulaC30H34N8O11S2
Molecular Weight746.77 g/mol
CategoryPharmacopoeial Impurity Standards / EP Impurities
AvailabilityIn Stock

Chemical Structure

Cefpirome Impurity 37 CAS CATO-C4X-120737 chemical structure

Description

CATO manufactures Cefpirome Impurity 37 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.

Cefpirome Impurity 37 (CAS CATO-C4X-120737) is a certified pharmaceutical impurity reference standard with the molecular formula C30H34N8O11S2 and a molecular weight of 746.77 g/mol.

The molecular framework of Cefpirome Impurity 37 (C30H34N8O11S2) is characterized by a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage. 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. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

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 FormulaC30H34N8O11S2
Molecular Weight746.77 g/mol
Purity>90%
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
Degree of Unsaturation (DBE)18.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
Nitrogen Atoms8
Sulfur Atoms2

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