N-Ethyl-1-(3-methoxyphenyl)cyclohexanamine Hydrochloride CAS 1797121-52-8

Purity 97%+In StockPharmaceutical Standards
CAS No.1797121-52-8
Molecular FormulaC15H23NO
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

N-Ethyl-1-(3-methoxyphenyl)cyclohexanamine Hydrochloride CAS 1797121-52-8 chemical structure

Description

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.

CATO supplies N-Ethyl-1-(3-methoxyphenyl)cyclohexanamine Hydrochloride (CAS 1797121-52-8), a certified reference material (molecular formula C15H23NOHCl, MW 269.81 g/mol) for analytical method development and quality control.

Based on its molecular formula C15H23NOHCl, N-Ethyl-1-(3-methoxyphenyl)cyclohexanamine Hydrochloride contains a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, chlorine substitution; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 269.81 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. The presence of an aromatic ring or conjugated system gives the compound characteristic absorption bands in the UV-Vis region, making it well suited to UV or diode-array detection (DAD).

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.

Physical & Chemical Properties

Molecular FormulaC15H23NO HCl
Molecular Weight269.81 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.)1994
Halogen ContentCl-containing
Nitrogen Atoms1

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