4-(tert-Butyl)-3-cyclopropoxy-5-(trifluoromethyl)pyridine CAS 1243463-85-5

Purity 97%+In StockPharmaceutical Standards
CAS No.1243463-85-5
Molecular FormulaC13H16F3NO
Molecular Weight259.27 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

4-(tert-Butyl)-3-cyclopropoxy-5-(trifluoromethyl)pyridine CAS 1243463-85-5 chemical structure

Description

The molecular framework of 4-(tert-Butyl)-3-cyclopropoxy-5-(trifluoromethyl)pyridine (C13H16F3NO) is characterized by a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, fluorine substitution. 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 high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

4-(tert-Butyl)-3-cyclopropoxy-5-(trifluoromethyl)pyridine (CAS 1243463-85-5), molecular formula C13H16F3NO and molecular weight 259.27 g/mol, is a CATO reference standard with documented purity and traceability.

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.

As a certified reference material (CRM), 4-(tert-Butyl)-3-cyclopropoxy-5-(trifluoromethyl)pyridine meets the metrological traceability requirements of ISO/IEC 17025 laboratories. Batch-to-batch consistency is monitored via control charts to guarantee comparable assigned values across lots.

Physical & Chemical Properties

Molecular FormulaC13H16F3NO
Molecular Weight259.27 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)5.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1990
Halogen ContentF-containing
Nitrogen Atoms1

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