2-amino-2-methyl-1-(2-methylphenyl)propan-1-one hydrochloride CAS 1864052-38-9

Purity 97%+In StockPharmaceutical Standards
CAS No.1864052-38-9
Molecular FormulaC11H15NO
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-amino-2-methyl-1-(2-methylphenyl)propan-1-one hydrochloride CAS 1864052-38-9 chemical structure

Description

CATO supplies 2-amino-2-methyl-1-(2-methylphenyl)propan-1-one hydrochloride (CAS 1864052-38-9), a certified reference material (molecular formula C11H15NOHCl, MW 213.70 g/mol) for analytical method development and quality control.

The molecular framework of 2-amino-2-methyl-1-(2-methylphenyl)propan-1-one hydrochloride (C11H15NOHCl) is characterized by a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, chlorine 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. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

Recommended for analytical method development and validation; each product is supplied with a full Certificate of Analysis (COA) ensuring ISO 17034 metrological traceability.

As a certified reference material (CRM), 2-amino-2-methyl-1-(2-methylphenyl)propan-1-one hydrochloride meets the metrological traceability requirements of ISO/IEC 17025 laboratories. Batch-to-batch consistency is monitored via control charts to guarantee comparable assigned values across lots.

Physical & Chemical Properties

Molecular FormulaC11H15NO HCl
Molecular Weight213.70 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.)1995
Halogen ContentCl-containing
Nitrogen Atoms1

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