2-(tert-Butyl)-6-(trifluoromethyl)quinoline-4-carbonitrile CAS 1416440-02-2

Purity 97%+In StockPharmaceutical Standards
CAS No.1416440-02-2
Molecular FormulaC15H13F3N2
Molecular Weight278.27 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-(tert-Butyl)-6-(trifluoromethyl)quinoline-4-carbonitrile CAS 1416440-02-2 chemical structure

Description

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.

CATO supplies 2-(tert-Butyl)-6-(trifluoromethyl)quinoline-4-carbonitrile (CAS 1416440-02-2), a certified reference material (molecular formula C15H13F3N2, MW 278.27 g/mol) for analytical method development and quality control.

The molecular framework of 2-(tert-Butyl)-6-(trifluoromethyl)quinoline-4-carbonitrile (C15H13F3N2) is characterized by a nitrogen-containing heterocyclic scaffold, a nitrile group, 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 aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

As a certified reference material (CRM), 2-(tert-Butyl)-6-(trifluoromethyl)quinoline-4-carbonitrile 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 FormulaC15H13F3N2
Molecular Weight278.27 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)9.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1991
Halogen ContentF-containing
Nitrogen Atoms2

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