Phenyl(2,4,6-trimethoxyphenyl)iodonium p-toluenesulfonate CAS 936326-60-2

Purity 97%+In StockPharmaceutical Standards
CAS No.936326-60-2
Molecular FormulaC15H16IO3
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Phenyl(2,4,6-trimethoxyphenyl)iodonium p-toluenesulfonate CAS 936326-60-2 chemical structure

Description

Compared with other compounds in its class, the molecular weight of 542.38 g/mol gives Phenyl(2,4,6-trimethoxyphenyl)iodonium p-toluenesulfonate distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

CATO supplies Phenyl(2,4,6-trimethoxyphenyl)iodonium p-toluenesulfonate (CAS 936326-60-2), a certified reference material (molecular formula C15H16IO3C7H7O3S, MW 542.38 g/mol) for analytical method development and quality control.

The molecular framework of Phenyl(2,4,6-trimethoxyphenyl)iodonium p-toluenesulfonate (C15H16IO3C7H7O3S) is characterized by a flavonoid core, a sulfone group, a hydroxyl group, an ether linkage, iodine substitution. 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. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

Recommended for analytical method development and validation; each product is supplied with a full Certificate of Analysis (COA) ensuring ISO 17034 metrological traceability.

CATO manufactures Phenyl(2,4,6-trimethoxyphenyl)iodonium p-toluenesulfonate 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 FormulaC15H16IO3 C7H7O3S
Molecular Weight542.38 g/mol
Purity97%+
StorageStore at room temperature, protect from light, keep sealed and dry
Solubility (reference)Soluble in methanol, acetonitrile, DMSO, water (slightly soluble)
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)11.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1987
Halogen ContentI-containing
Sulfur Atoms1

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