(4-Nitrophenyl)(2,4,6-trimethylphenyl)iodonium triflate CAS 1146127-11-8

Purity 97%+In StockPharmaceutical Standards
CAS No.1146127-11-8
Molecular FormulaC15H15INO2
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(4-Nitrophenyl)(2,4,6-trimethylphenyl)iodonium triflate CAS 1146127-11-8 chemical structure

Description

As a certified reference material (CRM), (4-Nitrophenyl)(2,4,6-trimethylphenyl)iodonium triflate meets the metrological traceability requirements of ISO/IEC 17025 laboratories. Batch-to-batch consistency is monitored via control charts to guarantee comparable assigned values across lots.

(4-Nitrophenyl)(2,4,6-trimethylphenyl)iodonium triflate (CAS 1146127-11-8), molecular formula C15H15INO2CF3O3S and molecular weight 517.25 g/mol, is a CATO reference standard with documented purity and traceability.

Owing to a flavonoid core, an amide group, a sulfone group, a hydroxyl group, an ether linkage, fluorine/iodine substitution, (4-Nitrophenyl)(2,4,6-trimethylphenyl)iodonium triflate is typically pale yellow to yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 517.25 g/mol — guide the selection of appropriate sample preparation and analytical techniques. 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).

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

Physical & Chemical Properties

Molecular FormulaC15H15INO2 CF3O3S
Molecular Weight517.25 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)8.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1989
Halogen ContentF/I-containing
Nitrogen Atoms1
Sulfur Atoms1

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Why CATO?