11H-Indeno[1,2-b]quinoline CAS 243-51-6

Purity 97%+In StockPharmaceutical Standards
CAS No.243-51-6
Molecular FormulaC16H11N
Molecular Weight217.27 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

11H-Indeno[1,2-b]quinoline CAS 243-51-6 chemical structure

Description

Under current pharmacopoeial and regulatory frameworks, quality-control requirements for this class of reference material explicitly involve the control of targets including 11H-Indeno[1,2-b]quinoline.

CATO supplies 11H-Indeno[1,2-b]quinoline (CAS 243-51-6), a certified reference material (molecular formula C16H11N, MW 217.27 g/mol) for analytical method development and quality control.

The molecular framework of 11H-Indeno[1,2-b]quinoline (C16H11N) 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 aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

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 11H-Indeno[1,2-b]quinoline 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 FormulaC16H11N
Molecular Weight217.27 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)12.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1957
Nitrogen Atoms1

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