2-Amino-1-(4-methylphenyl)-ethanone HCl CAS 5467-70-9

Purity 97%+In StockPharmaceutical Standards
CAS No.5467-70-9
Molecular FormulaC9H11NO
Molecular Weight149.19 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-Amino-1-(4-methylphenyl)-ethanone HCl CAS 5467-70-9 chemical structure

Description

The occurrence of 2-Amino-1-(4-methylphenyl)-ethanone HCl is closely related to a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage in its molecular formula, which determines its behaviour during synthesis, purification, or degradation.

CATO supplies 2-Amino-1-(4-methylphenyl)-ethanone HCl (CAS 5467-70-9), a certified reference material (molecular formula C9H11NO, MW 149.19 g/mol) for analytical method development and quality control.

Based on its molecular formula C9H11NO, 2-Amino-1-(4-methylphenyl)-ethanone HCl contains a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 149.19 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. 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 FormulaC9H11NO
Molecular Weight149.19 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in methanol, acetonitrile, DMSO, water (slightly soluble)
StabilityLight-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)5.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1958
Nitrogen Atoms1

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