4-Iodo-4',4''-dimethoxytriphenylamine CAS 201802-15-5

Purity 97%+In StockPharmaceutical Standards
CAS No.201802-15-5
Molecular FormulaC20H18INO2
Molecular Weight431.27 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

4-Iodo-4',4''-dimethoxytriphenylamine CAS 201802-15-5 chemical structure

Description

CATO supplies 4-Iodo-4',4''-dimethoxytriphenylamine (CAS 201802-15-5), a certified reference material (molecular formula C20H18INO2, MW 431.27 g/mol) for analytical method development and quality control.

Structurally, 4-Iodo-4',4''-dimethoxytriphenylamine (C20H18INO2) contains a steroid core, an amide group, a hydroxyl group, an ether linkage, iodine substitution. The molecule exhibits a degree of unsaturation (DBE) of 12.0, corresponding to approximately 12 ring(s) or double-bond equivalent(s). With a molecular weight of 431.27 g/mol, it falls into the moderately-high-molecular-weight range. 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.

As a certified reference material (CRM), 4-Iodo-4',4''-dimethoxytriphenylamine 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.

Physical & Chemical Properties

Molecular FormulaC20H18INO2
Molecular Weight431.27 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; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)12.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2014
Halogen ContentI-containing
Nitrogen Atoms1

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