2-[4-(sec-Butyl)phenoxy]-4-methylaniline CAS 946683-58-5

Purity 97%+In StockPharmaceutical Standards
CAS No.946683-58-5
Molecular FormulaC17H21NO
Molecular Weight255.35 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-[4-(sec-Butyl)phenoxy]-4-methylaniline CAS 946683-58-5 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 2-[4-(sec-Butyl)phenoxy]-4-methylaniline.

CATO supplies 2-[4-(sec-Butyl)phenoxy]-4-methylaniline (CAS 946683-58-5), a certified reference material (molecular formula C17H21NO, MW 255.35 g/mol) for analytical method development and quality control.

Structurally, 2-[4-(sec-Butyl)phenoxy]-4-methylaniline (C17H21NO) contains a steroid core, an amide group, a hydroxyl group, an ether linkage. The molecule exhibits a degree of unsaturation (DBE) of 8.0, corresponding to approximately 8 ring(s) or double-bond equivalent(s). With a molecular weight of 255.35 g/mol, it falls into the medium-molecular-weight range. The high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

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.

CATO manufactures 2-[4-(sec-Butyl)phenoxy]-4-methylaniline 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 FormulaC17H21NO
Molecular Weight255.35 g/mol
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)8.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1987
Nitrogen Atoms1

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