2-(4-Bromophenyl)-6-chloroimidazo[1,2-a]pyridine CAS 96464-10-7

Purity 97%+In StockPharmaceutical Standards
CAS No.96464-10-7
Molecular FormulaC13H8BrClN2
Molecular Weight307.57 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-(4-Bromophenyl)-6-chloroimidazo[1,2-a]pyridine CAS 96464-10-7 chemical structure

Description

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.

2-(4-Bromophenyl)-6-chloroimidazo[1,2-a]pyridine (CAS 96464-10-7) is a high-purity analytical reference standard with the molecular formula C13H8BrClN2 and a molecular weight of 307.57 g/mol.

2-(4-Bromophenyl)-6-chloroimidazo[1,2-a]pyridine (C13H8BrClN2) contains a nitrogen-containing heterocyclic scaffold, a nitrile group, chlorine/bromine substitution. Halogen substitution raises its density and boiling point, its high carbon-to-hydrogen ratio confers good lipid solubility; these physicochemical properties determine the optimal preparation and storage of its standard solutions. 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).

As a certified reference material (CRM), 2-(4-Bromophenyl)-6-chloroimidazo[1,2-a]pyridine meets the metrological traceability requirements of ISO/IEC 17025 laboratories. Batch-to-batch consistency is monitored via control charts to guarantee comparable assigned values across lots.

Physical & Chemical Properties

Molecular FormulaC13H8BrClN2
Molecular Weight307.57 g/mol
AppearancePale yellow to yellow crystalline powder. (slight halide-like odor, low volatility)
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)10.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1984
Halogen ContentCl/Br-containing
Nitrogen Atoms2

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