(-)-1-(2,5-Dimethoxy-4-iodophenyl)-2-aminopropane Hydrochloride CAS 82864-02-6

Purity 97%+In StockPharmaceutical Standards
CAS No.82864-02-6
Molecular FormulaC11H16INO2
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(-)-1-(2,5-Dimethoxy-4-iodophenyl)-2-aminopropane Hydrochloride CAS 82864-02-6 chemical structure

Description

CATO manufactures (-)-1-(2,5-Dimethoxy-4-iodophenyl)-2-aminopropane 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.

(-)-1-(2,5-Dimethoxy-4-iodophenyl)-2-aminopropane Hydrochloride (CAS 82864-02-6) is a high-purity analytical reference standard with the molecular formula C11H16INO2HCl and a molecular weight of 357.61 g/mol.

Based on its molecular formula C11H16INO2HCl, (-)-1-(2,5-Dimethoxy-4-iodophenyl)-2-aminopropane Hydrochloride contains an amide group, a carboxylic acid group, a hydroxyl group, an ether linkage, chlorine/iodine substitution; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 357.61 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

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.

Physical & Chemical Properties

Molecular FormulaC11H16INO2 HCl
Molecular Weight357.61 g/mol
AppearanceWhite to pale yellow crystalline powder. (slight halide-like odor, low volatility)
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)3.0
UV AbsorptionUV-absorbing
CAS Registry Year (est.)1980
Halogen ContentCl/I-containing
Nitrogen Atoms1

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