2-((4-Fluorophenyl)thio)-1-(4-hydroxy-3,5-dimethylphenyl)ethan-1-one CAS 339100-31-1

Purity 97%+In StockPharmaceutical Standards
CAS No.339100-31-1
Molecular FormulaC16H15FO2S
Molecular Weight290.35 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-((4-Fluorophenyl)thio)-1-(4-hydroxy-3,5-dimethylphenyl)ethan-1-one CAS 339100-31-1 chemical structure

Description

CATO supplies 2-((4-Fluorophenyl)thio)-1-(4-hydroxy-3,5-dimethylphenyl)ethan-1-one (CAS 339100-31-1), a certified reference material (molecular formula C16H15FO2S, MW 290.35 g/mol) for analytical method development and quality control.

The molecular framework of 2-((4-Fluorophenyl)thio)-1-(4-hydroxy-3,5-dimethylphenyl)ethan-1-one (C16H15FO2S) is characterized by a sulfone group, a carboxylic acid group, a hydroxyl group, an ether linkage, fluorine substitution, a polycyclic aromatic system. 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 aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

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-((4-Fluorophenyl)thio)-1-(4-hydroxy-3,5-dimethylphenyl)ethan-1-one 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 FormulaC16H15FO2S
Molecular Weight290.35 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, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)9.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2025
Halogen ContentF-containing
Sulfur Atoms1

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