2,2,2-Trifluoro-1-(2,3,4,5-tetramethylphenyl)ethan-1-amine CAS 886371-42-2

Purity 97%+In StockPharmaceutical Standards
CAS No.886371-42-2
Molecular FormulaC12H16F3N
Molecular Weight231.26 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2,2,2-Trifluoro-1-(2,3,4,5-tetramethylphenyl)ethan-1-amine CAS 886371-42-2 chemical structure

Description

Recommended for analytical method development and validation; each product is supplied with a full Certificate of Analysis (COA) ensuring ISO 17034 metrological traceability.

CATO supplies 2,2,2-Trifluoro-1-(2,3,4,5-tetramethylphenyl)ethan-1-amine (CAS 886371-42-2), a certified reference material (molecular formula C12H16F3N, MW 231.26 g/mol) for analytical method development and quality control.

Based on its molecular formula C12H16F3N, 2,2,2-Trifluoro-1-(2,3,4,5-tetramethylphenyl)ethan-1-amine contains a nitrogen-containing heterocyclic scaffold, a nitrile group, fluorine substitution; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 231.26 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

CATO manufactures 2,2,2-Trifluoro-1-(2,3,4,5-tetramethylphenyl)ethan-1-amine under ISO 17034:2016 accreditation with dual CNAS and ANAB accreditation. Each batch is characterized by orthogonal methods and supplied with a full Certificate of Analysis (COA), ensuring metrological traceability.

Physical & Chemical Properties

Molecular FormulaC12H16F3N
Molecular Weight231.26 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)4.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1987
Halogen ContentF-containing
Nitrogen Atoms1

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