2-[1-(4-Ethoxybenzyl)-2-piperazinyl]ethanoldihydrochloride CAS 1273578-03-2

Purity 97%+In StockPharmaceutical Standards
CAS No.1273578-03-2
Molecular FormulaC15H24N2O2
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-[1-(4-Ethoxybenzyl)-2-piperazinyl]ethanoldihydrochloride CAS 1273578-03-2 chemical structure

Description

CATO supplies 2-[1-(4-Ethoxybenzyl)-2-piperazinyl]ethanoldihydrochloride (CAS 1273578-03-2), a certified reference material (molecular formula C15H24N2O2HCl, MW 300.83 g/mol) for analytical method development and quality control.

The molecular framework of 2-[1-(4-Ethoxybenzyl)-2-piperazinyl]ethanoldihydrochloride (C15H24N2O2HCl) 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. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

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

CATO manufactures 2-[1-(4-Ethoxybenzyl)-2-piperazinyl]ethanoldihydrochloride 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 FormulaC15H24N2O2 2*HCl
Molecular Weight300.83 g/mol
AppearanceOff-white to pale yellow crystalline powder. (slight halide-like odor)
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Hygroscopic; reseal immediately after opening; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)4.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1990
Halogen ContentCl-containing
Nitrogen Atoms2

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