2-(tert-Butyl)-3-(cyclohexyloxy)phenol CAS 1243363-97-4

Purity 97%+In StockPharmaceutical Standards
CAS No.1243363-97-4
Molecular FormulaC16H24O2
Molecular Weight248.36 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-(tert-Butyl)-3-(cyclohexyloxy)phenol CAS 1243363-97-4 chemical structure

Description

The occurrence of 2-(tert-Butyl)-3-(cyclohexyloxy)phenol is closely related to a carboxylic acid group, a hydroxyl group, an ether linkage, an aromatic ring system in its molecular formula, which determines its behaviour during synthesis, purification, or degradation.

CATO supplies 2-(tert-Butyl)-3-(cyclohexyloxy)phenol (CAS 1243363-97-4), a certified reference material (molecular formula C16H24O2, MW 248.36 g/mol) for analytical method development and quality control.

Based on its molecular formula C16H24O2, 2-(tert-Butyl)-3-(cyclohexyloxy)phenol contains a carboxylic acid group, a hydroxyl group, an ether linkage, an aromatic ring system; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 248.36 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. The high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

Recommended for analytical method development and validation; each product is supplied with a full Certificate of Analysis (COA) ensuring ISO 17034 metrological traceability.

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 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.)1990

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