[(2E)-3-(2-Methoxyphenyl)prop-2-en-1-yl](propyl)amine hydrochloride CAS 1240590-98-0

Purity 97%+In StockPharmaceutical Standards
CAS No.1240590-98-0
Molecular FormulaC13H19NO
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

[(2E)-3-(2-Methoxyphenyl)prop-2-en-1-yl](propyl)amine hydrochloride CAS 1240590-98-0 chemical structure

Description

As a certified reference material (CRM), [(2E)-3-(2-Methoxyphenyl)prop-2-en-1-yl](propyl)amine 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.

CATO supplies [(2E)-3-(2-Methoxyphenyl)prop-2-en-1-yl](propyl)amine hydrochloride (CAS 1240590-98-0), a certified reference material (molecular formula C13H19NOHCl, MW 241.76 g/mol) for analytical method development and quality control.

The molecular framework of [(2E)-3-(2-Methoxyphenyl)prop-2-en-1-yl](propyl)amine hydrochloride (C13H19NOHCl) 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.

Physical & Chemical Properties

Molecular FormulaC13H19NO HCl
Molecular Weight241.76 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.)1990
Halogen ContentCl-containing
Nitrogen Atoms1

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