(S)-1-(3-(trifluoromethyl)phenyl)butan-1-amine CAS 1194056-03-5

Purity 97%+In StockPharmaceutical Standards
CAS No.1194056-03-5
Molecular FormulaC11H14F3N
Molecular Weight217.23 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(S)-1-(3-(trifluoromethyl)phenyl)butan-1-amine CAS 1194056-03-5 chemical structure

Description

The occurrence of (S)-1-(3-(trifluoromethyl)phenyl)butan-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 (S)-1-(3-(trifluoromethyl)phenyl)butan-1-amine (CAS 1194056-03-5), a certified reference material (molecular formula C11H14F3N, MW 217.23 g/mol) for analytical method development and quality control.

Structurally, (S)-1-(3-(trifluoromethyl)phenyl)butan-1-amine (C11H14F3N) contains a nitrogen-containing heterocyclic scaffold, a nitrile group, fluorine substitution. The molecule exhibits a degree of unsaturation (DBE) of 4.0, corresponding to approximately 4 ring(s) or double-bond equivalent(s). With a molecular weight of 217.23 g/mol, it falls into the medium-molecular-weight range. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

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 FormulaC11H14F3N
Molecular Weight217.23 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.)1989
Halogen ContentF-containing
Nitrogen Atoms1

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