Phenyl 6-methyl-2-(p-tolyl)quinoline-4-carboxylate CAS 355419-81-7

Purity 97%+In StockPharmaceutical Standards
CAS No.355419-81-7
Molecular FormulaC24H19NO2
Molecular Weight353.41 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Phenyl 6-methyl-2-(p-tolyl)quinoline-4-carboxylate CAS 355419-81-7 chemical structure

Description

Under current pharmacopoeial and regulatory frameworks, quality-control requirements for this class of reference material explicitly involve the control of targets including Phenyl 6-methyl-2-(p-tolyl)quinoline-4-carboxylate.

Phenyl 6-methyl-2-(p-tolyl)quinoline-4-carboxylate (CAS 355419-81-7), molecular formula C24H19NO2 and molecular weight 353.41 g/mol, is a CATO reference standard with documented purity and traceability.

Based on its molecular formula C24H19NO2, Phenyl 6-methyl-2-(p-tolyl)quinoline-4-carboxylate contains a steroid core, an amide group, a hydroxyl group, an ether linkage; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 353.41 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. 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), Phenyl 6-methyl-2-(p-tolyl)quinoline-4-carboxylate 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 FormulaC24H19NO2
Molecular Weight353.41 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)16.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2025
Nitrogen Atoms1

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