2,2,4,8-tetramethyl-1,2,3,4-tetrahydroquinoline CAS 4497-61-4

Purity 97%+In StockPharmaceutical Standards
CAS No.4497-61-4
Molecular FormulaC13H19N
Molecular Weight189.30 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2,2,4,8-tetramethyl-1,2,3,4-tetrahydroquinoline CAS 4497-61-4 chemical structure

Description

Recommended for analytical method development and validation; each product is supplied with a full Certificate of Analysis (COA) ensuring ISO 17034 metrological traceability.

CATO supplies 2,2,4,8-tetramethyl-1,2,3,4-tetrahydroquinoline (CAS 4497-61-4), a certified reference material (molecular formula C13H19N, MW 189.30 g/mol) for analytical method development and quality control.

The molecular framework of 2,2,4,8-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 presence of an aromatic ring or conjugated system gives the compound characteristic absorption bands in the UV-Vis region, making it well suited to UV or diode-array detection (DAD).

CATO manufactures 2,2,4,8-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.)1958
Nitrogen Atoms1

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