(S)-1-(3-fluoro-4-(trifluoromethyl)phenyl)-2-methylpropan-1-amine CAS 1212863-81-4

Purity 97%+In StockPharmaceutical Standards
CAS No.1212863-81-4
Molecular FormulaC11H13F4N
Molecular Weight235.22 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(S)-1-(3-fluoro-4-(trifluoromethyl)phenyl)-2-methylpropan-1-amine CAS 1212863-81-4 chemical structure

Description

CATO supplies (S)-1-(3-fluoro-4-(trifluoromethyl)phenyl)-2-methylpropan-1-amine (CAS 1212863-81-4), a certified reference material (molecular formula C11H13F4N, MW 235.22 g/mol) for analytical method development and quality control.

(S)-1-(3-fluoro-4-(trifluoromethyl)phenyl)-2-methylpropan-1-amine (C11H13F4N) 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.

CATO manufactures (S)-1-(3-fluoro-4-(trifluoromethyl)phenyl)-2-methylpropan-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 FormulaC11H13F4N
Molecular Weight235.22 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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