4-(tert-Butyl)-2-(cyclohexyloxy)phenol CAS 610278-80-3

Purity 97%+In StockPharmaceutical Standards
CAS No.610278-80-3
Molecular FormulaC16H24O2
Molecular Weight248.36 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

4-(tert-Butyl)-2-(cyclohexyloxy)phenol CAS 610278-80-3 chemical structure

Description

Compared with other compounds in its class, the molecular weight of 248.36 g/mol gives 4-(tert-Butyl)-2-(cyclohexyloxy)phenol distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

4-(tert-Butyl)-2-(cyclohexyloxy)phenol (CAS 610278-80-3) is a high-purity analytical reference standard with the molecular formula C16H24O2 and a molecular weight of 248.36 g/mol.

The molecular framework of 4-(tert-Butyl)-2-(cyclohexyloxy)phenol (C16H24O2) is characterized by a carboxylic acid group, a hydroxyl group, an ether linkage, an aromatic ring system. In reversed-phase chromatography, its retention is governed primarily by its high hydrophobicity (logP), which provides a practical basis for HPLC-UV/DAD or LC-MS method development. 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 4-(tert-Butyl)-2-(cyclohexyloxy)phenol 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 FormulaC16H24O2
Molecular Weight248.36 g/mol
AppearanceOff-white to pale yellow crystalline powder
Purity97%+
StorageStore at room temperature
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityMay oxidize slowly on prolonged air exposure
Degree of Unsaturation (DBE)5.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1985

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