N-(3-Ethoxyphenyl)-2-iodoacetamide CAS 17641-14-4

Purity 97%+In StockPharmaceutical Standards
CAS No.17641-14-4
Molecular FormulaC10H12INO2
Molecular Weight305.11 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

N-(3-Ethoxyphenyl)-2-iodoacetamide CAS 17641-14-4 chemical structure

Description

CATO supplies N-(3-Ethoxyphenyl)-2-iodoacetamide (CAS 17641-14-4), a certified reference material (molecular formula C10H12INO2, MW 305.11 g/mol) for analytical method development and quality control.

N-(3-Ethoxyphenyl)-2-iodoacetamide (C10H12INO2) contains a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, iodine substitution. Halogen substitution raises its density and boiling point, its high carbon-to-hydrogen ratio confers good lipid solubility, the carboxyl group imparts weak acidity; these physicochemical properties determine the optimal preparation and storage of its standard solutions. 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 N-(3-Ethoxyphenyl)-2-iodoacetamide 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 FormulaC10H12INO2
Molecular Weight305.11 g/mol
AppearanceOff-white to pale yellow crystalline powder. (slight halide-like odor, faint amine-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)5.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1962
Halogen ContentI-containing
Nitrogen Atoms1

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