(4-Isobutylphenyl)(p-tolyl)iodonium hexafluorophosphate(V) CAS 344562-80-7

Purity 97%+In StockPharmaceutical Standards
CAS No.344562-80-7
Molecular FormulaC17H20I
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(4-Isobutylphenyl)(p-tolyl)iodonium hexafluorophosphate(V) CAS 344562-80-7 chemical structure

Description

Based on its molecular formula C17H20IF6P, (4-Isobutylphenyl)(p-tolyl)iodonium hexafluorophosphate(V) contains organophosphorus functionality, fluorine/iodine substitution, an aromatic ring system; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 496.21 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. The high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

CATO supplies (4-Isobutylphenyl)(p-tolyl)iodonium hexafluorophosphate(V) (CAS 344562-80-7), a certified reference material (molecular formula C17H20IF6P, MW 496.21 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 (4-Isobutylphenyl)(p-tolyl)iodonium hexafluorophosphate(V) 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 FormulaC17H20I F6P
Molecular Weight496.21 g/mol
AppearanceOff-white to pale yellow crystalline powder. (slight halide-like odor, low volatility)
Purity97%+
StorageStore at room temperature
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate
StabilityMay oxidize slowly on prolonged air exposure
Degree of Unsaturation (DBE)4.5
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2025
Halogen ContentF/I-containing

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