4-(1,2,3,4-Tetrahydroisoquinolin-2-yl)benzoic acid CAS 1020933-05-4

Purity 97%+In StockPharmaceutical Standards
CAS No.1020933-05-4
Molecular FormulaC16H15NO2
Molecular Weight253.30 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

4-(1,2,3,4-Tetrahydroisoquinolin-2-yl)benzoic acid CAS 1020933-05-4 chemical structure

Description

The occurrence of 4-(1,2,3,4-Tetrahydroisoquinolin-2-yl)benzoic acid is closely related to a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage in its molecular formula, which determines its behaviour during synthesis, purification, or degradation.

CATO supplies 4-(1,2,3,4-Tetrahydroisoquinolin-2-yl)benzoic acid (CAS 1020933-05-4), a certified reference material (molecular formula C16H15NO2, MW 253.30 g/mol) for analytical method development and quality control.

The molecular framework of 4-(1,2,3,4-Tetrahydroisoquinolin-2-yl)benzoic acid (C16H15NO2) is characterized by a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage. 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. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

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

The assigned purity is verified by mass-balance and quantitative NMR (qNMR) approaches, with the expanded uncertainty reported at a 95% confidence level (k=2). Batch homogeneity and stability are independently assessed for every lot.

Physical & Chemical Properties

Molecular FormulaC16H15NO2
Molecular Weight253.30 g/mol
AppearancePale yellow to 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)10.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1988
Nitrogen Atoms1

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