6-Methyl-1-phenyl-1,2,3,4-tetrahydroisoquinoline CAS 220327-29-7

Purity 97%+In StockPharmaceutical Standards
CAS No.220327-29-7
Molecular FormulaC16H17N
Molecular Weight223.31 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

6-Methyl-1-phenyl-1,2,3,4-tetrahydroisoquinoline CAS 220327-29-7 chemical structure

Description

CATO supplies 6-Methyl-1-phenyl-1,2,3,4-tetrahydroisoquinoline (CAS 220327-29-7), a certified reference material (molecular formula C16H17N, MW 223.31 g/mol) for analytical method development and quality control.

The molecular framework of 6-Methyl-1-phenyl-1,2,3,4-tetrahydroisoquinoline (C16H17N) 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).

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 6-Methyl-1-phenyl-1,2,3,4-tetrahydroisoquinoline 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 FormulaC16H17N
Molecular Weight223.31 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)9.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2019
Nitrogen Atoms1

Recommended Standards

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