2-(tert-Butoxy)-3-isopropoxyphenol CAS 1243405-04-0

Purity 97%+In StockPharmaceutical Standards
CAS No.1243405-04-0
Molecular FormulaC13H20O3
Molecular Weight224.30 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-(tert-Butoxy)-3-isopropoxyphenol CAS 1243405-04-0 chemical structure

Description

Compared with other compounds in its class, the molecular weight of 224.30 g/mol gives 2-(tert-Butoxy)-3-isopropoxyphenol distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

CATO supplies 2-(tert-Butoxy)-3-isopropoxyphenol (CAS 1243405-04-0), a certified reference material (molecular formula C13H20O3, MW 224.30 g/mol) for analytical method development and quality control.

Owing to a carboxylic acid group, a hydroxyl group, an ether linkage, an aromatic ring system, 2-(tert-Butoxy)-3-isopropoxyphenol is typically off-white to pale yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 224.30 g/mol — guide the selection of appropriate sample preparation and analytical techniques. 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.

CATO manufactures 2-(tert-Butoxy)-3-isopropoxyphenol 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 FormulaC13H20O3
Molecular Weight224.30 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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