3-(tert-Butoxy)-5-(trifluoromethyl)aniline CAS 1369841-47-3

Purity 97%+In StockPharmaceutical Standards
CAS No.1369841-47-3
Molecular FormulaC11H14F3NO
Molecular Weight233.23 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3-(tert-Butoxy)-5-(trifluoromethyl)aniline CAS 1369841-47-3 chemical structure

Description

Compared with other compounds in its class, the molecular weight of 233.23 g/mol gives 3-(tert-Butoxy)-5-(trifluoromethyl)aniline distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

3-(tert-Butoxy)-5-(trifluoromethyl)aniline (CAS 1369841-47-3), molecular formula C11H14F3NO and molecular weight 233.23 g/mol, is a CATO reference standard with documented purity and traceability.

Owing to a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, fluorine substitution, 3-(tert-Butoxy)-5-(trifluoromethyl)aniline is typically off-white to pale yellow low-melting solid. Its solid-state physicochemical attributes — including a molecular weight of 233.23 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.

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 FormulaC11H14F3NO
Molecular Weight233.23 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep tightly closed to prevent evaporation
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)4.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1991
Halogen ContentF-containing
Nitrogen Atoms1

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