Bedaquiline Impurity 63 CAS 2813341-31-8

Purity 97%+In StockPharmacopoeial Impurity Standards
CAS No.2813341-31-8
Molecular FormulaC16H14BrNO2
Molecular Weight332.19 g/mol
CategoryPharmacopoeial Impurity Standards / EP Impurities
AvailabilityIn Stock

Chemical Structure

Bedaquiline Impurity 63 CAS 2813341-31-8 chemical structure

Description

CATO manufactures Bedaquiline Impurity 63 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 Bedaquiline Impurity 63 (CAS 2813341-31-8), a pharmacopoeial impurity reference standard (molecular formula C16H14BrNO2, MW 332.19 g/mol) used for the identification and quantification of trace impurities in APIs.

The molecular framework of Bedaquiline Impurity 63 (C16H14BrNO2) is characterized by a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, bromine substitution. In reversed-phase chromatography, its retention is governed primarily by its high hydrophobicity (logP), 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 FormulaC16H14BrNO2
Molecular Weight332.19 g/mol
AppearancePale yellow to yellow crystalline powder. (slight halide-like odor)
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)10.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2003
Halogen ContentBr-containing
Nitrogen Atoms1

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