4-(4-(Tert-butyl)phenyl)-4-oxo-2-((5-(trifluoromethyl)pyridin-2-yl)thio)butanoic acid CAS 279691-64-4

Purity 97%+In StockPharmaceutical Standards
CAS No.279691-64-4
Molecular FormulaC20H20F3NO3S
Molecular Weight411.44 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

4-(4-(Tert-butyl)phenyl)-4-oxo-2-((5-(trifluoromethyl)pyridin-2-yl)thio)butanoic acid CAS 279691-64-4 chemical structure

Description

CATO supplies 4-(4-(Tert-butyl)phenyl)-4-oxo-2-((5-(trifluoromethyl)pyridin-2-yl)thio)butanoic acid (CAS 279691-64-4), a certified reference material (molecular formula C20H20F3NO3S, MW 411.44 g/mol) for analytical method development and quality control.

The molecular framework of 4-(4-(Tert-butyl)phenyl)-4-oxo-2-((5-(trifluoromethyl)pyridin-2-yl)thio)butanoic acid (C20H20F3NO3S) is characterized by a steroid core, an amide group, a sulfone group, a hydroxyl group, an ether linkage, fluorine 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. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

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 4-(4-(Tert-butyl)phenyl)-4-oxo-2-((5-(trifluoromethyl)pyridin-2-yl)thio)butanoic 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 FormulaC20H20F3NO3S
Molecular Weight411.44 g/mol
Purity97%+
StorageStore at room temperature, protect from light, keep sealed and dry
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)10.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2025
Halogen ContentF-containing
Nitrogen Atoms1
Sulfur Atoms1

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