Candesartan Cilexetil Impurity 36 CAS CATO-C4X-123436

Purity 97%+In StockPharmacopoeial Impurity Standards
CAS No.CATO-C4X-123436
Molecular FormulaC15H13NO
Molecular Weight223.27 g/mol
CategoryPharmacopoeial Impurity Standards / EP Impurities
AvailabilityIn Stock

Chemical Structure

Candesartan Cilexetil Impurity 36 CAS CATO-C4X-123436 chemical structure

Description

CATO manufactures Candesartan Cilexetil Impurity 36 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.

Candesartan Cilexetil Impurity 36 (CAS CATO-C4X-123436) is a certified pharmaceutical impurity reference standard with the molecular formula C15H13NO and a molecular weight of 223.27 g/mol.

Structurally, Candesartan Cilexetil Impurity 36 (C15H13NO) contains a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage. The molecule exhibits a degree of unsaturation (DBE) of 10.0, corresponding to approximately 10 ring(s) or double-bond equivalent(s). With a molecular weight of 223.27 g/mol, it falls into the medium-molecular-weight range. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

Recommended for quantitative analysis by HPLC, GC, LC-MS/MS, or GC-MS as an external calibration standard; it can also be used for spiked-recovery experiments, LOD/LOQ determination, and LC-MS/MS multiple-reaction-monitoring (MRM) calibration.

Physical & Chemical Properties

Molecular FormulaC15H13NO
Molecular Weight223.27 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityLight-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)10.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
Nitrogen Atoms1

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