3-(tert-Butoxy)-5-cyclopropoxyaniline CAS 1243371-60-9

Purity 97%+In StockPharmaceutical Standards
CAS No.1243371-60-9
Molecular FormulaC13H19NO2
Molecular Weight221.30 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3-(tert-Butoxy)-5-cyclopropoxyaniline CAS 1243371-60-9 chemical structure

Description

The occurrence of 3-(tert-Butoxy)-5-cyclopropoxyaniline is closely related to a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage in its molecular formula, which determines its behaviour during synthesis, purification, or degradation.

CATO supplies 3-(tert-Butoxy)-5-cyclopropoxyaniline (CAS 1243371-60-9), a certified reference material (molecular formula C13H19NO2, MW 221.30 g/mol) for analytical method development and quality control.

3-(tert-Butoxy)-5-cyclopropoxyaniline (C13H19NO2) contains a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage. Its high carbon-to-hydrogen ratio confers good lipid solubility, the carboxyl group imparts weak acidity; these physicochemical properties determine the optimal preparation and storage of its standard solutions. 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 3-(tert-Butoxy)-5-cyclopropoxyaniline 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 FormulaC13H19NO2
Molecular Weight221.30 g/mol
AppearanceOff-white to pale yellow crystalline powder
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)5.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1990
Nitrogen Atoms1

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