1-(tert-Butoxy)-3-cyclopropoxy-5-isopropoxybenzene CAS 1243458-63-0

Purity 97%+In StockPharmaceutical Standards
CAS No.1243458-63-0
Molecular FormulaC16H24O3
Molecular Weight264.36 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

1-(tert-Butoxy)-3-cyclopropoxy-5-isopropoxybenzene CAS 1243458-63-0 chemical structure

Description

Compared with other compounds in its class, the molecular weight of 264.36 g/mol gives 1-(tert-Butoxy)-3-cyclopropoxy-5-isopropoxybenzene distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

CATO supplies 1-(tert-Butoxy)-3-cyclopropoxy-5-isopropoxybenzene (CAS 1243458-63-0), a certified reference material (molecular formula C16H24O3, MW 264.36 g/mol) for analytical method development and quality control.

The molecular framework of 1-(tert-Butoxy)-3-cyclopropoxy-5-isopropoxybenzene (C16H24O3) 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 aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

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 FormulaC16H24O3
Molecular Weight264.36 g/mol
AppearanceOff-white to pale yellow crystalline powder
Purity97%+
StorageStore at room temperature, keep sealed and dry
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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