5-(4-(Trifluoromethyl)phenyl)pyrimidin-2-amine CAS 1111104-89-2

Purity 97%+In StockPharmaceutical Standards
CAS No.1111104-89-2
Molecular FormulaC11H8F3N3
Molecular Weight239.20 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

5-(4-(Trifluoromethyl)phenyl)pyrimidin-2-amine CAS 1111104-89-2 chemical structure

Description

As a certified reference material (CRM), 5-(4-(Trifluoromethyl)phenyl)pyrimidin-2-amine 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 5-(4-(Trifluoromethyl)phenyl)pyrimidin-2-amine (CAS 1111104-89-2), a certified reference material (molecular formula C11H8F3N3, MW 239.20 g/mol) for analytical method development and quality control.

The molecular framework of 5-(4-(Trifluoromethyl)phenyl)pyrimidin-2-amine (C11H8F3N3) 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 presence of an aromatic ring or conjugated system gives the compound characteristic absorption bands in the UV-Vis region, making it well suited to UV or diode-array detection (DAD).

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 FormulaC11H8F3N3
Molecular Weight239.20 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)8.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1989
Halogen ContentF-containing
Nitrogen Atoms3

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