2,6-Bis(6-(tert-butyl)naphthalen-2-yl)anthracene CAS 1086103-33-4

Purity 97%+In StockPharmaceutical Standards
CAS No.1086103-33-4
Molecular FormulaC42H38
Molecular Weight542.75 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2,6-Bis(6-(tert-butyl)naphthalen-2-yl)anthracene CAS 1086103-33-4 chemical structure

Description

The occurrence of 2,6-Bis(6-(tert-butyl)naphthalen-2-yl)anthracene is closely related to a polycyclic aromatic system in its molecular formula, which determines its behaviour during synthesis, purification, or degradation.

CATO supplies 2,6-Bis(6-(tert-butyl)naphthalen-2-yl)anthracene (CAS 1086103-33-4), a certified reference material (molecular formula C42H38, MW 542.75 g/mol) for analytical method development and quality control.

Owing to a polycyclic aromatic system, 2,6-Bis(6-(tert-butyl)naphthalen-2-yl)anthracene is typically pale yellow to yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 542.75 g/mol — guide the selection of appropriate sample preparation and analytical techniques. 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 2,6-Bis(6-(tert-butyl)naphthalen-2-yl)anthracene 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 FormulaC42H38
Molecular Weight542.75 g/mol
AppearancePale yellow to yellow crystalline powder
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)24.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1989

Recommended Standards

Why CATO?