N-(4-Hydroxyphenyl)-3-(4-methoxyphenyl)acrylamide CAS 19186-86-8

Purity 97%+In StockPharmaceutical Standards
CAS No.19186-86-8
Molecular FormulaC16H15NO3
Molecular Weight269.30 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

N-(4-Hydroxyphenyl)-3-(4-methoxyphenyl)acrylamide CAS 19186-86-8 chemical structure

Description

Under current pharmacopoeial and regulatory frameworks, quality-control requirements for this class of reference material explicitly involve the control of targets including N-(4-Hydroxyphenyl)-3-(4-methoxyphenyl)acrylamide.

CATO supplies N-(4-Hydroxyphenyl)-3-(4-methoxyphenyl)acrylamide (CAS 19186-86-8), a certified reference material (molecular formula C16H15NO3, MW 269.30 g/mol) for analytical method development and quality control.

N-(4-Hydroxyphenyl)-3-(4-methoxyphenyl)acrylamide (C16H15NO3) contains a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage. 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.

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 FormulaC16H15NO3
Molecular Weight269.30 g/mol
AppearancePale yellow to yellow crystalline powder
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry
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)10.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1962
Nitrogen Atoms1

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