(R)-1-(4-Butylphenyl)-2,2,2-trifluoroethan-1-amine CAS 1213699-26-3

Purity 97%+In StockPharmaceutical Standards
CAS No.1213699-26-3
Molecular FormulaC12H16F3N
Molecular Weight231.26 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(R)-1-(4-Butylphenyl)-2,2,2-trifluoroethan-1-amine CAS 1213699-26-3 chemical structure

Description

The occurrence of (R)-1-(4-Butylphenyl)-2,2,2-trifluoroethan-1-amine is closely related to a nitrogen-containing heterocyclic scaffold, a nitrile group, fluorine substitution in its molecular formula, which determines its behaviour during synthesis, purification, or degradation.

CATO supplies (R)-1-(4-Butylphenyl)-2,2,2-trifluoroethan-1-amine (CAS 1213699-26-3), a certified reference material (molecular formula C12H16F3N, MW 231.26 g/mol) for analytical method development and quality control.

Owing to a nitrogen-containing heterocyclic scaffold, a nitrile group, fluorine substitution, (R)-1-(4-Butylphenyl)-2,2,2-trifluoroethan-1-amine is typically off-white to pale yellow low-melting solid. Its solid-state physicochemical attributes — including a molecular weight of 231.26 g/mol — guide the selection of appropriate sample preparation and analytical techniques. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

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.

The assigned purity is verified by mass-balance and quantitative NMR (qNMR) approaches, with the expanded uncertainty reported at a 95% confidence level (k=2). Batch homogeneity and stability are independently assessed for every lot.

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.)1990
Halogen ContentF-containing
Nitrogen Atoms1

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