3-(Trifluoromethyl)phenyl trifluoromethanesulfonate CAS 199188-30-2

Purity 97%+In StockPharmaceutical Standards
CAS No.199188-30-2
Molecular FormulaC8H4F6O3S
Molecular Weight294.17 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3-(Trifluoromethyl)phenyl trifluoromethanesulfonate CAS 199188-30-2 chemical structure

Description

The molecular framework of 3-(Trifluoromethyl)phenyl trifluoromethanesulfonate (C8H4F6O3S) is characterized by a sulfone group, a carboxylic acid group, a hydroxyl group, an ether linkage, fluorine substitution, an aromatic ring system. In reversed-phase chromatography, its retention is governed primarily by the polarity and ionization state of its functional groups, which provides a practical basis for HPLC-UV/DAD or LC-MS method development. The presence of an aromatic ring or conjugated system gives the compound characteristic absorption bands in the UV-Vis region, making it well suited to UV or diode-array detection (DAD).

CATO supplies 3-(Trifluoromethyl)phenyl trifluoromethanesulfonate (CAS 199188-30-2), a certified reference material (molecular formula C8H4F6O3S, MW 294.17 g/mol) for analytical method development and quality control.

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 3-(Trifluoromethyl)phenyl trifluoromethanesulfonate 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 FormulaC8H4F6O3S
Molecular Weight294.17 g/mol
Purity97%+
StorageStore in a cool place (≤25°C), keep sealed and dry, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in methanol, ethanol, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Hygroscopic; reseal immediately after opening; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)4.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2013
Halogen ContentF-containing
Sulfur Atoms1

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