3-[(4-Iodophenyl)amino]-2-phenyl-1H-inden-1-one CAS 22009-03-6

Purity 97%+In StockPharmaceutical Standards
CAS No.22009-03-6
Molecular FormulaC21H14INO
Molecular Weight423.25 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3-[(4-Iodophenyl)amino]-2-phenyl-1H-inden-1-one CAS 22009-03-6 chemical structure

Description

The occurrence of 3-[(4-Iodophenyl)amino]-2-phenyl-1H-inden-1-one is closely related to a steroid core, an amide group, a hydroxyl group, an ether linkage, iodine substitution in its molecular formula, which determines its behaviour during synthesis, purification, or degradation.

CATO supplies 3-[(4-Iodophenyl)amino]-2-phenyl-1H-inden-1-one (CAS 22009-03-6), a certified reference material (molecular formula C21H14INO, MW 423.25 g/mol) for analytical method development and quality control.

The molecular framework of 3-[(4-Iodophenyl)amino]-2-phenyl-1H-inden-1-one (C21H14INO) is characterized by a steroid core, an amide group, a hydroxyl group, an ether linkage, iodine substitution. In reversed-phase chromatography, its retention is governed primarily by its high hydrophobicity (logP), which provides a practical basis for HPLC-UV/DAD or LC-MS method development. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

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

The assigned purity is verified by mass-balance and quantitative NMR (qNMR) approaches, with the expanded uncertainty reported at a 95% confidence level (k=2). Batch homogeneity and stability are independently assessed for every lot.

Physical & Chemical Properties

Molecular FormulaC21H14INO
Molecular Weight423.25 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)15.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1963
Halogen ContentI-containing
Nitrogen Atoms1

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