n-Benzyl-2-hydroxy-5-iodobenzamide CAS 13156-80-4

Purity 97%+In StockPharmaceutical Standards
CAS No.13156-80-4
Molecular FormulaC14H12INO2
Molecular Weight353.16 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

n-Benzyl-2-hydroxy-5-iodobenzamide CAS 13156-80-4 chemical structure

Description

CATO supplies n-Benzyl-2-hydroxy-5-iodobenzamide (CAS 13156-80-4), a certified reference material (molecular formula C14H12INO2, MW 353.16 g/mol) for analytical method development and quality control.

The molecular framework of n-Benzyl-2-hydroxy-5-iodobenzamide (C14H12INO2) is characterized by a nitrogen-containing heterocyclic scaffold, 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. The high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

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 FormulaC14H12INO2
Molecular Weight353.16 g/mol
AppearancePale yellow to yellow crystalline powder. (slight halide-like odor)
Purity97%+
StorageStore at 2-8°C, 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)9.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1960
Halogen ContentI-containing
Nitrogen Atoms1

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