122648-99-1

Basic information

• Product Name: 9,10-Di(2-naphthyl)anthracene
• Synonyms: 9,10-DI-NAPHTHALEN-2-YL-ANTHRACENE;9,10-DI-(2-NAPHTHYL)ANTHRACENE;9,10-BIS-(2-NAPHTHYL)-ANTHRACENE;ADN;9,10-Di-beta-naphthylanthracene;9,10-Di-(2-naphthyl);ADN, 9,10-Di(2-naphthyl)anthracene;9,10-Di(2-naphthyl)anthracene (AND)
• CAS NO: 122648-99-1
• Molecular Formula: C34H22
• Molecular Weight: 430.54
• EINECS: 1312995-182-4
• Product Categories: electronic;White powder;oled materials;fine chemicals, specialty chemicals, intermediates, electronic chemical, organic synthesis, pharmaceutical intermediates;OLED materrials
• Mol File: 122648-99-1.mol
• Article Data: 6

Chemical Properties

• Melting Point: 382~384°C
• Boiling Point: 595.39 °C at 760 mmHg
• Flash Point: 314.818 °C
• Appearance: Off-white powder
• Density: 1.208 g/cm³
• Vapor Pressure: 0mmHg at 25°C
• Refractive Index: 1.761
• Storage Temp.: Sealed in dry,Room Temperature
• Solubility: slightly sol. in Tetrahydrofuran
• CAS DataBase Reference: 9,10-Di(2-naphthyl)anthracene(CAS DataBase Reference)
• NIST Chemistry Reference: 9,10-Di(2-naphthyl)anthracene(122648-99-1)
• EPA Substance Registry System: 9,10-Di(2-naphthyl)anthracene(122648-99-1)

Safety Data

• Hazard Codes: Xn
• Statements: 36/37/38-22
• Safety Statements: 26-36/37/39
• WGK Germany: 3
• Hazardous Substances Data: 122648-99-1(Hazardous Substances Data)

Usage

Classification

Electron transporting materials, Light emitter layer materials, Phosphorescent host materials; Light-emitting diodes, Organic electronics.

Applications

9,10-Bis(2-naphthyl)anthracene (ADN), which is well known for its high thermal and morphological stability, is widely used as the host material for blue OLEDs. However, with the development of the co-doping technology*, 9,10-Bis(2-naphthyl)anthrace has also shown to be a promising host material for full colour OLEDs due to its wide energy band gap.

Description

9,10-Bis(2-naphthyl)anthracene (ADN), which is well known for its high thermal and morphological stability, is widely used as the host material for blue OLEDs [1, 2].

Uses

9,10-Di(2-naphthyl)anthracene is an organic light emitting diode material.

InChI:InChI=1/C34H22/c1-3-11-25-21-27(19-17-23(25)9-1)33-29-13-5-7-15-31(29)34(32-16-8-6-14-30(32)33)28-20-18-24-10-2-4-12-26(24)22-28/h1-22H

Upstream product

• 523-27-3 9,10-Dibromoanthracene 
• 256652-04-7 4,4,5,5-tetramethyl-2-(naphthalen-2-yl)-1,3,2-dioxaborolane 
• 580-13-2 2-bromonaphthalene 
• 84-65-1 9,10-phenanthrenequinone 
• 873377-70-9 9,10-di-[2]naphthyl-9,10-dihydro-anthracene-9,10-diol 

Relevant articles and documents

ORGANIC ELECTROLUMINESCENCE DEVICE AND DISPLAY DEVICE INCLUDING THE SAME

Provided are an organic electroluminescence device and a display device including the same. The organic electroluminescence device includes a polycyclic compound represented by Formula 1 in a hole blocking layer and at least one of a first light emitting layer and an electron transport layer, wherein each of Y1 to Y5 and Y11 to Y15 is independently CH or N, at least four of Y1 to Y5 are CH, at least four of Y11 to Y15 are CH, and R1, R2, and R3 are as disclosed in the description.

BENZOPHENANTHRENE DERIVATIVE AND ORGANIC ELECTROLUMINESCENT DEVICE EMPLOYING THE SAME

A fused aromatic ring derivative shown by the following formula (1): wherein Ra and Rb are independently a hydrogen atom or a substituent, p is an integer of 1 to 8 and q is an integer of 1 to 11, when p is 2 or more, plural Ra

Arylpyrene compounds

One embodiment of the present invention provides an organic light emitting device comprising an anode, a cathode, and an organic layer disposed between the anode and the cathode, wherein the organic layer comprises an arylpyrene compound. In another embodiment, the present invention also provides organic light emitting devices comprising an anode, a cathode, and an organic layer disposed between the anode and the cathode, wherein the organic layer comprises an arylpyrene compound doped in an anthracene host, preferably ADN. Another embodiment of the present invention provides specific arylpyrene compounds.