N-(2,4-dimethoxybenzyl)-1,2,3,4-tetrahydronaphthalen-1-amine hydrobromide CAS 1609407-35-3

Purity 97%+In StockPharmaceutical Standards
CAS No.1609407-35-3
Molecular FormulaC19H23NO2
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

N-(2,4-dimethoxybenzyl)-1,2,3,4-tetrahydronaphthalen-1-amine hydrobromide CAS 1609407-35-3 chemical structure

Description

CATO supplies N-(2,4-dimethoxybenzyl)-1,2,3,4-tetrahydronaphthalen-1-amine hydrobromide (CAS 1609407-35-3), a certified reference material (molecular formula C19H23NO2HBr, MW 378.31 g/mol) for analytical method development and quality control.

Owing to a steroid core, an amide group, a hydroxyl group, an ether linkage, bromine substitution, N-(2,4-dimethoxybenzyl)-1,2,3,4-tetrahydronaphthalen-1-amine hydrobromide is typically pale yellow to yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 378.31 g/mol — guide the selection of appropriate sample preparation and analytical techniques. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

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 N-(2,4-dimethoxybenzyl)-1,2,3,4-tetrahydronaphthalen-1-amine hydrobromide 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 FormulaC19H23NO2 HBr
Molecular Weight378.31 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)8.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1993
Halogen ContentBr-containing
Nitrogen Atoms1

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