1-(1,2,3,4-Tetrahydroquinolin-7-yl)ethan-1-one CAS 147265-75-6

Purity 97%+In StockPharmaceutical Standards
CAS No.147265-75-6
Molecular FormulaC11H13NO
Molecular Weight175.23 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

1-(1,2,3,4-Tetrahydroquinolin-7-yl)ethan-1-one CAS 147265-75-6 chemical structure

Description

Compared with other compounds in its class, the molecular weight of 175.23 g/mol gives 1-(1,2,3,4-Tetrahydroquinolin-7-yl)ethan-1-one distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

1-(1,2,3,4-Tetrahydroquinolin-7-yl)ethan-1-one (CAS 147265-75-6) is a high-purity analytical reference standard with the molecular formula C11H13NO and a molecular weight of 175.23 g/mol.

The molecular framework of 1-(1,2,3,4-Tetrahydroquinolin-7-yl)ethan-1-one (C11H13NO) 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. 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).

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.

As a certified reference material (CRM), 1-(1,2,3,4-Tetrahydroquinolin-7-yl)ethan-1-one meets the metrological traceability requirements of ISO/IEC 17025 laboratories. Batch-to-batch consistency is monitored via control charts to guarantee comparable assigned values across lots.

Physical & Chemical Properties

Molecular FormulaC11H13NO
Molecular Weight175.23 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityLight-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)6.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1999
Nitrogen Atoms1

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