6,6,12,12-Tetramethyl-6,12-dihydroindeno[1,2-b]fluorene CAS 872705-63-0

Purity 97%+In StockPharmaceutical Standards
CAS No.872705-63-0
Molecular FormulaC24H22
Molecular Weight310.43 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

6,6,12,12-Tetramethyl-6,12-dihydroindeno[1,2-b]fluorene CAS 872705-63-0 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 6,6,12,12-Tetramethyl-6,12-dihydroindeno[1,2-b]fluorene.

CATO supplies 6,6,12,12-Tetramethyl-6,12-dihydroindeno[1,2-b]fluorene (CAS 872705-63-0), a certified reference material (molecular formula C24H22, MW 310.43 g/mol) for analytical method development and quality control.

The molecular framework of 6,6,12,12-Tetramethyl-6,12-dihydroindeno[1,2-b]fluorene (C24H22) is characterized by a polycyclic aromatic system. 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).

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.

CATO manufactures 6,6,12,12-Tetramethyl-6,12-dihydroindeno[1,2-b]fluorene 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 FormulaC24H22
Molecular Weight310.43 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
StabilityLight-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)14.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1987

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