3,4-Di-tert-butoxyphenol CAS 1243395-09-6

Purity 97%+In StockPharmaceutical Standards
CAS No.1243395-09-6
Molecular FormulaC14H22O3
Molecular Weight238.32 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3,4-Di-tert-butoxyphenol CAS 1243395-09-6 chemical structure

Description

Compared with other compounds in its class, the molecular weight of 238.32 g/mol gives 3,4-Di-tert-butoxyphenol distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

CATO supplies 3,4-Di-tert-butoxyphenol (CAS 1243395-09-6), a certified reference material (molecular formula C14H22O3, MW 238.32 g/mol) for analytical method development and quality control.

The molecular framework of 3,4-Di-tert-butoxyphenol (C14H22O3) 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.

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 FormulaC14H22O3
Molecular Weight238.32 g/mol
AppearanceOff-white to pale yellow crystalline powder
Purity97%+
StorageStore in a cool place (≤25°C), keep sealed and dry
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Hygroscopic; reseal immediately after opening
Degree of Unsaturation (DBE)4.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1990

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