2-Amino-2-methyl-N-(3-methylphenethyl)propanamide hydrochloride CAS 1568930-33-5

Purity 97%+In StockPharmaceutical Standards
CAS No.1568930-33-5
Molecular FormulaC13H20N2O
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-Amino-2-methyl-N-(3-methylphenethyl)propanamide hydrochloride CAS 1568930-33-5 chemical structure

Description

The molecular framework of 2-Amino-2-methyl-N-(3-methylphenethyl)propanamide hydrochloride (C13H20N2OHCl) 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. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

2-Amino-2-methyl-N-(3-methylphenethyl)propanamide hydrochloride (CAS 1568930-33-5) is a high-purity analytical reference standard with the molecular formula C13H20N2OHCl and a molecular weight of 256.77 g/mol.

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 2-Amino-2-methyl-N-(3-methylphenethyl)propanamide hydrochloride 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 FormulaC13H20N2O HCl
Molecular Weight256.77 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in DMSO, DMF, methanol
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.)1993
Halogen ContentCl-containing
Nitrogen Atoms2

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