(R)-2-methyl-1-(3-(trifluoromethoxy)phenyl)propan-1-amine CAS 1213613-65-0

Purity 97%+In StockPharmaceutical Standards
CAS No.1213613-65-0
Molecular FormulaC11H14F3NO
Molecular Weight233.23 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(R)-2-methyl-1-(3-(trifluoromethoxy)phenyl)propan-1-amine CAS 1213613-65-0 chemical structure

Description

(R)-2-methyl-1-(3-(trifluoromethoxy)phenyl)propan-1-amine (CAS 1213613-65-0) is a high-purity analytical reference standard with the molecular formula C11H14F3NO and a molecular weight of 233.23 g/mol.

The molecular framework of (R)-2-methyl-1-(3-(trifluoromethoxy)phenyl)propan-1-amine (C11H14F3NO) is characterized by a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, 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 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.

CATO manufactures (R)-2-methyl-1-(3-(trifluoromethoxy)phenyl)propan-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 FormulaC11H14F3NO
Molecular Weight233.23 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, DMSO
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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