4-(4-Hexyloxybenzoyl)quinoline CAS 1706436-21-6

Purity 97%+In StockPharmaceutical Standards
CAS No.1706436-21-6
Molecular FormulaC22H23NO2
Molecular Weight333.42 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

4-(4-Hexyloxybenzoyl)quinoline CAS 1706436-21-6 chemical structure

Description

As a certified reference material (CRM), 4-(4-Hexyloxybenzoyl)quinoline 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.

CATO supplies 4-(4-Hexyloxybenzoyl)quinoline (CAS 1706436-21-6), a certified reference material (molecular formula C22H23NO2, MW 333.42 g/mol) for analytical method development and quality control.

The molecular framework of 4-(4-Hexyloxybenzoyl)quinoline (C22H23NO2) is characterized by a steroid core, an amide group, a hydroxyl group, an ether linkage. 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. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

Recommended for analytical method development and validation; each product is supplied with a full Certificate of Analysis (COA) ensuring ISO 17034 metrological traceability.

Physical & Chemical Properties

Molecular FormulaC22H23NO2
Molecular Weight333.42 g/mol
AppearancePale yellow to yellow crystalline powder
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
Degree of Unsaturation (DBE)12.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1994
Nitrogen Atoms1

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