2,2,4-Trimethyl-7-(trifluoromethyl)-1,2-dihydroquinoline CAS 1242835-50-2

Purity 97%+In StockPharmaceutical Standards
CAS No.1242835-50-2
Molecular FormulaC13H14F3N
Molecular Weight241.25 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2,2,4-Trimethyl-7-(trifluoromethyl)-1,2-dihydroquinoline CAS 1242835-50-2 chemical structure

Description

As a certified reference material (CRM), 2,2,4-Trimethyl-7-(trifluoromethyl)-1,2-dihydroquinoline 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.

CATO supplies 2,2,4-Trimethyl-7-(trifluoromethyl)-1,2-dihydroquinoline (CAS 1242835-50-2), a certified reference material (molecular formula C13H14F3N, MW 241.25 g/mol) for analytical method development and quality control.

2,2,4-Trimethyl-7-(trifluoromethyl)-1,2-dihydroquinoline (C13H14F3N) contains a nitrogen-containing heterocyclic scaffold, a nitrile group, fluorine substitution. Halogen substitution raises its density and boiling point, its high carbon-to-hydrogen ratio confers good lipid solubility; these physicochemical properties determine the optimal preparation and storage of its standard solutions. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

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.

Physical & Chemical Properties

Molecular FormulaC13H14F3N
Molecular Weight241.25 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
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)6.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1990
Halogen ContentF-containing
Nitrogen Atoms1

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