4-(4-Bromo-3-methylphenyl)-2-chloropyridine CAS 1539429-62-3

Purity 97%+In StockPharmaceutical Standards
CAS No.1539429-62-3
Molecular FormulaC12H9BrClN
Molecular Weight282.56 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

4-(4-Bromo-3-methylphenyl)-2-chloropyridine CAS 1539429-62-3 chemical structure

Description

CATO manufactures 4-(4-Bromo-3-methylphenyl)-2-chloropyridine 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.

4-(4-Bromo-3-methylphenyl)-2-chloropyridine (CAS 1539429-62-3), molecular formula C12H9BrClN and molecular weight 282.56 g/mol, is a CATO reference standard with documented purity and traceability.

The molecular framework of 4-(4-Bromo-3-methylphenyl)-2-chloropyridine (C12H9BrClN) is characterized by a nitrogen-containing heterocyclic scaffold, a nitrile group, chlorine/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. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

This reference standard is suitable for quantitative analysis on major chromatographic platforms including HPLC, GC, LC-MS/MS, and GC-MS, serving as an external calibration standard or a system suitability test reference material.

Physical & Chemical Properties

Molecular FormulaC12H9BrClN
Molecular Weight282.56 g/mol
AppearancePale yellow to yellow crystalline powder. (slight halide-like odor, low volatility)
Purity97%+
StorageStore at 2-8°C, protect from light, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)8.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1992
Halogen ContentCl/Br-containing
Nitrogen Atoms1

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