(2-Hydroxy-5-methylphenyl)triphenylphosphonium iodide CAS 2005487-70-5

Purity 97%+In StockPharmaceutical Standards
CAS No.2005487-70-5
Molecular FormulaC25H22OP
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(2-Hydroxy-5-methylphenyl)triphenylphosphonium iodide CAS 2005487-70-5 chemical structure

Description

CATO supplies (2-Hydroxy-5-methylphenyl)triphenylphosphonium iodide (CAS 2005487-70-5), a certified reference material (molecular formula C25H22OPI, MW 496.32 g/mol) for analytical method development and quality control.

Owing to a steroid core, organophosphorus functionality, a hydroxyl group, an ether linkage, iodine substitution, (2-Hydroxy-5-methylphenyl)triphenylphosphonium iodide is typically pale yellow to yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 496.32 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.

CATO manufactures (2-Hydroxy-5-methylphenyl)triphenylphosphonium iodide 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 FormulaC25H22OP I
Molecular Weight496.32 g/mol
AppearancePale yellow to yellow crystalline powder. (slight halide-like odor)
Purity97%+
StorageStore at room temperature, protect from light
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)14.5
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1996
Halogen ContentI-containing

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