3-Isopropoxy-N-[4-(phenethyloxy)benzyl]aniline CAS 1040684-68-1

Purity 97%+In StockPharmaceutical Standards
CAS No.1040684-68-1
Molecular FormulaC24H27NO2
Molecular Weight361.48 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3-Isopropoxy-N-[4-(phenethyloxy)benzyl]aniline CAS 1040684-68-1 chemical structure

Description

The occurrence of 3-Isopropoxy-N-[4-(phenethyloxy)benzyl]aniline 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 3-Isopropoxy-N-[4-(phenethyloxy)benzyl]aniline (CAS 1040684-68-1), a certified reference material (molecular formula C24H27NO2, MW 361.48 g/mol) for analytical method development and quality control.

3-Isopropoxy-N-[4-(phenethyloxy)benzyl]aniline (C24H27NO2) contains a steroid core, 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 aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

This reference standard is suitable for quantitative analysis on major chromatographic platforms including HPLC, GC, LC-MS/MS, and GC-MS, serving as an external calibration standard or a system suitability test reference material.

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 FormulaC24H27NO2
Molecular Weight361.48 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
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)12.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1988
Nitrogen Atoms1

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