Topiroxostat Impurity 49 CAS 14906-59-3

Purity >95%In StockPharmacopoeial Impurity Standards
CAS No.14906-59-3
Molecular FormulaC6H4N2O
Molecular Weight120.11 g/mol
CategoryPharmacopoeial Impurity Standards / EP Impurities
AvailabilityIn Stock

Chemical Structure

Topiroxostat Impurity 49 CAS 14906-59-3 chemical structure

Description

CATO manufactures Topiroxostat Impurity 49 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 Topiroxostat Impurity 49 (CAS 14906-59-3), a pharmacopoeial impurity reference standard (molecular formula C6H4N2O, MW 120.11 g/mol) used for the identification and quantification of trace impurities in APIs.

The molecular framework of Topiroxostat Impurity 49 (C6H4N2O) is characterized by an amide group, a hydroxyl group, an ether linkage, an aromatic ring system. 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 presence of an aromatic ring or conjugated system gives the compound characteristic absorption bands in the UV-Vis region, making it well suited to UV or diode-array detection (DAD).

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 FormulaC6H4N2O
Molecular Weight120.11 g/mol
Purity>95%
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityLight-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)6.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1961
Nitrogen Atoms2

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