3,4-(Dibenzyloxy)phenethylamine hydrochloride CAS 1699-56-5

Purity 97%+In StockPharmaceutical Standards
CAS No.1699-56-5
Molecular FormulaC22H23NO2
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3,4-(Dibenzyloxy)phenethylamine hydrochloride CAS 1699-56-5 chemical structure

Description

CATO supplies 3,4-(Dibenzyloxy)phenethylamine hydrochloride (CAS 1699-56-5), a certified reference material (molecular formula C22H23NO2HCl, MW 369.89 g/mol) for analytical method development and quality control.

Based on its molecular formula C22H23NO2HCl, 3,4-(Dibenzyloxy)phenethylamine hydrochloride contains a steroid core, an amide group, a hydroxyl group, an ether linkage, chlorine substitution; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 369.89 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. The high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

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), 3,4-(Dibenzyloxy)phenethylamine 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 FormulaC22H23NO2 HCl
Molecular Weight369.89 g/mol
AppearancePale yellow to yellow crystalline powder. (slight halide-like odor)
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)11.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1957
Halogen ContentCl-containing
Nitrogen Atoms1

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