3,3,6-Trimethyl-1,2,3,4-tetrahydroisoquinoline hydrochloride CAS 1909327-58-7

Purity 97%+In StockPharmaceutical Standards
CAS No.1909327-58-7
Molecular FormulaC12H17N
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3,3,6-Trimethyl-1,2,3,4-tetrahydroisoquinoline hydrochloride CAS 1909327-58-7 chemical structure

Description

CATO supplies 3,3,6-Trimethyl-1,2,3,4-tetrahydroisoquinoline hydrochloride (CAS 1909327-58-7), a certified reference material (molecular formula C12H17NHCl, MW 211.73 g/mol) for analytical method development and quality control.

Based on its molecular formula C12H17NHCl, 3,3,6-Trimethyl-1,2,3,4-tetrahydroisoquinoline hydrochloride contains a nitrogen-containing heterocyclic scaffold, a nitrile group, chlorine substitution; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 211.73 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

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 manufactures 3,3,6-Trimethyl-1,2,3,4-tetrahydroisoquinoline 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.

Physical & Chemical Properties

Molecular FormulaC12H17N HCl
Molecular Weight211.73 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
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.)1995
Halogen ContentCl-containing
Nitrogen Atoms1

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