3-(tert-Butyl)-2-cyclopropoxy-N-methylaniline CAS 1243406-97-4

Purity 97%+In StockPharmaceutical Standards
CAS No.1243406-97-4
Molecular FormulaC14H21NO
Molecular Weight219.32 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3-(tert-Butyl)-2-cyclopropoxy-N-methylaniline CAS 1243406-97-4 chemical structure

Description

The occurrence of 3-(tert-Butyl)-2-cyclopropoxy-N-methylaniline 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-Butyl)-2-cyclopropoxy-N-methylaniline (CAS 1243406-97-4), a certified reference material (molecular formula C14H21NO, MW 219.32 g/mol) for analytical method development and quality control.

Owing to a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, 3-(tert-Butyl)-2-cyclopropoxy-N-methylaniline is typically off-white to pale yellow low-melting solid. Its solid-state physicochemical attributes — including a molecular weight of 219.32 g/mol — guide the selection of appropriate sample preparation and analytical techniques. 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.

CATO manufactures 3-(tert-Butyl)-2-cyclopropoxy-N-methylaniline 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 FormulaC14H21NO
Molecular Weight219.32 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityLight-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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