(E)-3-(4-isobutylphenyl)-N-(1-phenylethyl)acrylamide CAS 329778-69-0

Purity 97%+In StockPharmaceutical Standards
CAS No.329778-69-0
Molecular FormulaC21H25NO
Molecular Weight307.43 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(E)-3-(4-isobutylphenyl)-N-(1-phenylethyl)acrylamide CAS 329778-69-0 chemical structure

Description

The occurrence of (E)-3-(4-isobutylphenyl)-N-(1-phenylethyl)acrylamide is closely related to a steroid core, an amide group, a hydroxyl group, an ether linkage in its molecular formula, which determines its behaviour during synthesis, purification, or degradation.

CATO supplies (E)-3-(4-isobutylphenyl)-N-(1-phenylethyl)acrylamide (CAS 329778-69-0), a certified reference material (molecular formula C21H25NO, MW 307.43 g/mol) for analytical method development and quality control.

(E)-3-(4-isobutylphenyl)-N-(1-phenylethyl)acrylamide (C21H25NO) contains a steroid core, an amide group, a hydroxyl group, an ether linkage. Its high carbon-to-hydrogen ratio confers good lipid solubility; these physicochemical properties determine the optimal preparation and storage of its standard solutions. 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.

As a certified reference material (CRM), (E)-3-(4-isobutylphenyl)-N-(1-phenylethyl)acrylamide 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 FormulaC21H25NO
Molecular Weight307.43 g/mol
AppearancePale yellow to yellow crystalline powder
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityLight-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)10.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2025
Nitrogen Atoms1

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