2-Butyl-4-chloroquinoline CAS 144624-27-1

Purity 97%+In StockPharmaceutical Standards
CAS No.144624-27-1
Molecular FormulaC13H14ClN
Molecular Weight219.71 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-Butyl-4-chloroquinoline CAS 144624-27-1 chemical structure

Description

Compared with other compounds in its class, the molecular weight of 219.71 g/mol gives 2-Butyl-4-chloroquinoline distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

CATO supplies 2-Butyl-4-chloroquinoline (CAS 144624-27-1), a certified reference material (molecular formula C13H14ClN, MW 219.71 g/mol) for analytical method development and quality control.

The molecular framework of 2-Butyl-4-chloroquinoline (C13H14ClN) is characterized by a nitrogen-containing heterocyclic scaffold, a nitrile group, chlorine 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 high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

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.

As a certified reference material (CRM), 2-Butyl-4-chloroquinoline 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 FormulaC13H14ClN
Molecular Weight219.71 g/mol
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)7.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1998
Halogen ContentCl-containing
Nitrogen Atoms1

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