(4-Methoxyphenyl)(phenyl)iodonium trifluoromethanesulfonate CAS 115298-63-0

Purity 97%+In StockPharmaceutical Standards
CAS No.115298-63-0
Molecular FormulaC13H12IO
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(4-Methoxyphenyl)(phenyl)iodonium trifluoromethanesulfonate CAS 115298-63-0 chemical structure

Description

CATO manufactures (4-Methoxyphenyl)(phenyl)iodonium 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.

CATO supplies (4-Methoxyphenyl)(phenyl)iodonium trifluoromethanesulfonate (CAS 115298-63-0), a certified reference material (molecular formula C13H12IOCF3O3S, MW 460.20 g/mol) for analytical method development and quality control.

Based on its molecular formula C13H12IOCF3O3S, (4-Methoxyphenyl)(phenyl)iodonium trifluoromethanesulfonate contains a sulfone group, a carboxylic acid group, a hydroxyl group, an ether linkage, fluorine/iodine substitution, a polycyclic aromatic system; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 460.20 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. 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.

Physical & Chemical Properties

Molecular FormulaC13H12IO CF3O3S
Molecular Weight460.20 g/mol
Purity97%+
StorageStore in a cool place (≤25°C), 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; Hygroscopic; reseal immediately after opening; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)7.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1989
Halogen ContentF/I-containing
Sulfur Atoms1

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