2,2,4,6-Tetramethyl-1,2,3,4-tetrahydroquinoline CAS 16489-89-7

Purity 97%+In StockPharmaceutical Standards
CAS No.16489-89-7
Molecular FormulaC13H19N
Molecular Weight189.30 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2,2,4,6-Tetramethyl-1,2,3,4-tetrahydroquinoline CAS 16489-89-7 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 2,2,4,6-Tetramethyl-1,2,3,4-tetrahydroquinoline (CAS 16489-89-7), a certified reference material (molecular formula C13H19N, MW 189.30 g/mol) for analytical method development and quality control.

The molecular framework of 2,2,4,6-Tetramethyl-1,2,3,4-tetrahydroquinoline (C13H19N) is characterized by a nitrogen-containing heterocyclic scaffold, a nitrile group. 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 high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

CATO manufactures 2,2,4,6-Tetramethyl-1,2,3,4-tetrahydroquinoline 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 FormulaC13H19N
Molecular Weight189.30 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate
StabilityLight-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)5.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1961
Nitrogen Atoms1

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