2-(4-Methyl-1H-pyrazol-1-yl)-2-phenylethan-1-amine hydrochloride CAS 2490705-35-4

Purity 97%+In StockPharmaceutical Standards
CAS No.2490705-35-4
Molecular FormulaC12H15N3
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-(4-Methyl-1H-pyrazol-1-yl)-2-phenylethan-1-amine hydrochloride CAS 2490705-35-4 chemical structure

Description

The molecular framework of 2-(4-Methyl-1H-pyrazol-1-yl)-2-phenylethan-1-amine hydrochloride (C12H15N3HCl) is characterized by a nitrogen-containing heterocyclic scaffold, a nitrile group, 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. 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).

CATO supplies 2-(4-Methyl-1H-pyrazol-1-yl)-2-phenylethan-1-amine hydrochloride (CAS 2490705-35-4), a certified reference material (molecular formula C12H15N3HCl, MW 237.73 g/mol) for analytical method development and quality control.

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-(4-Methyl-1H-pyrazol-1-yl)-2-phenylethan-1-amine 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 FormulaC12H15N3 HCl
Molecular Weight237.73 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)6.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2000
Halogen ContentCl-containing
Nitrogen Atoms3

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