6,7-Dimethoxy-3,4-dihydroisoquinoline CAS 3382-18-1

Purity 97%+In StockPharmaceutical Standards
CAS No.3382-18-1
Molecular FormulaC11H13NO2
Molecular Weight191.23 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

6,7-Dimethoxy-3,4-dihydroisoquinoline CAS 3382-18-1 chemical structure

Description

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.

CATO supplies 6,7-Dimethoxy-3,4-dihydroisoquinoline (CAS 3382-18-1), a certified reference material (molecular formula C11H13NO2, MW 191.23 g/mol) for analytical method development and quality control.

Based on its molecular formula C11H13NO2, 6,7-Dimethoxy-3,4-dihydroisoquinoline contains an amino-acid-derived structure, an amide group, a hydroxyl group, an ether linkage; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 191.23 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.

CATO manufactures 6,7-Dimethoxy-3,4-dihydroisoquinoline 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 FormulaC11H13NO2
Molecular Weight191.23 g/mol
AppearanceOff-white to pale yellow crystalline powder
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
Degree of Unsaturation (DBE)6.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1957
Nitrogen Atoms1

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