N-(4-Aminophenyl)-2-[2-(sec-butyl)phenoxy]-butanamide CAS 1020055-97-3

Purity 97%+In StockPharmaceutical Standards
CAS No.1020055-97-3
Molecular FormulaC20H26N2O2
Molecular Weight326.43 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

N-(4-Aminophenyl)-2-[2-(sec-butyl)phenoxy]-butanamide CAS 1020055-97-3 chemical structure

Description

CATO supplies N-(4-Aminophenyl)-2-[2-(sec-butyl)phenoxy]-butanamide (CAS 1020055-97-3), a certified reference material (molecular formula C20H26N2O2, MW 326.43 g/mol) for analytical method development and quality control.

Owing to a steroid core, an amide group, a hydroxyl group, an ether linkage, N-(4-Aminophenyl)-2-[2-(sec-butyl)phenoxy]-butanamide is typically pale yellow to yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 326.43 g/mol — guide the selection of appropriate sample preparation and analytical techniques. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

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.

As a certified reference material (CRM), N-(4-Aminophenyl)-2-[2-(sec-butyl)phenoxy]-butanamide 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 FormulaC20H26N2O2
Molecular Weight326.43 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 DMSO, DMF, methanol
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Hygroscopic; reseal immediately after opening
Degree of Unsaturation (DBE)9.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1988
Nitrogen Atoms2

Related N Standards

Recommended Standards

Why CATO?