2-((4-Fluorobenzyl)thio)benzoic acid CAS 329063-99-2

Purity 97%+In StockPharmaceutical Standards
CAS No.329063-99-2
Molecular FormulaC14H11FO2S
Molecular Weight262.30 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-((4-Fluorobenzyl)thio)benzoic acid CAS 329063-99-2 chemical structure

Description

Compared with other compounds in its class, the molecular weight of 262.30 g/mol gives 2-((4-Fluorobenzyl)thio)benzoic acid distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

2-((4-Fluorobenzyl)thio)benzoic acid (CAS 329063-99-2), molecular formula C14H11FO2S and molecular weight 262.30 g/mol, is a CATO reference standard with documented purity and traceability.

The molecular framework of 2-((4-Fluorobenzyl)thio)benzoic acid (C14H11FO2S) 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 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.

CATO manufactures 2-((4-Fluorobenzyl)thio)benzoic acid under ISO 17034:2016 accreditation with dual CNAS and ANAB accreditation. Each batch is characterized by orthogonal methods and supplied with a full Certificate of Analysis (COA), ensuring metrological traceability.

Physical & Chemical Properties

Molecular FormulaC14H11FO2S
Molecular Weight262.30 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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