1-(7-([9,9'-Bianthracen]-10-yl)-9,9-dihexyl-9H-fluoren-2-yl)pyrene CAS 1705571-71-6

Purity 97%+In StockPharmaceutical Standards
CAS No.1705571-71-6
Molecular FormulaC69H58
Molecular Weight887.20 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

1-(7-([9,9'-Bianthracen]-10-yl)-9,9-dihexyl-9H-fluoren-2-yl)pyrene CAS 1705571-71-6 chemical structure

Description

Compared with other compounds in its class, the molecular weight of 887.20 g/mol gives 1-(7-([9,9'-Bianthracen]-10-yl)-9,9-dihexyl-9H-fluoren-2-yl)pyrene distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

CATO supplies 1-(7-([9,9'-Bianthracen]-10-yl)-9,9-dihexyl-9H-fluoren-2-yl)pyrene (CAS 1705571-71-6), a certified reference material (molecular formula C69H58, MW 887.20 g/mol) for analytical method development and quality control.

The molecular framework of 1-(7-([9,9'-Bianthracen]-10-yl)-9,9-dihexyl-9H-fluoren-2-yl)pyrene (C69H58) 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 high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

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 1-(7-([9,9'-Bianthracen]-10-yl)-9,9-dihexyl-9H-fluoren-2-yl)pyrene 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 FormulaC69H58
Molecular Weight887.20 g/mol
Purity97%+
StorageStore at room temperature, protect from light
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate
StabilityLight-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)41.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1994

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