α-ADN

α-ADN - Names and Identifiers

Name	9,10-Di(1-naphthyl)anthracene
Synonyms	α-ADN 9,10-Di-(1-naphthyl) 9,10-Di(-α-naphthyl)anthracen 9,10-Di(1-naphthyl)anthracene 9,10-DI-(1-NAPHTHYL)ANTHRACENE Anthracene, 9,10-di-1-naphthyl- 9,10-Di(naphthalen-1-yl)anthracen 9,10-DI-NAPHTHALEN-1-YL-ANTHRACENE 9,10-di(naphthalen-1-yl)anthracene anthracene, 9,10-di-1-naphthalenyl- Anthracene, 9,10-di-1-naphthalenyl- 9,10-Di(1-naphthyl)anthracene (purified by sublimation) 9,10-Di(1-naphthayl)anthracene (purified by sublimation)
CAS	26979-27-1
EINECS	1312995-182-4
InChI	InChI=1/C34H22/c1-3-15-25-23(11-1)13-9-21-27(25)33-29-17-5-7-19-31(29)34(32-20-8-6-18-30(32)33)28-22-10-14-24-12-2-4-16-26(24)28/h1-22H
InChIKey	GWNJZSGBZMLRBW-UHFFFAOYSA-N

α-ADN - Physico-chemical Properties

Molecular Formula	C34H22
Molar Mass	430.54
Density	1?+-.0.06 g/cm3(Predicted)
Melting Point	360°C(lit.)
Boling Point	577.5±45.0 °C(Predicted)
Flash Point	304.1°C
Vapor Presure	9.82E-13mmHg at 25°C
Maximum wavelength(λmax)	417nm(EtOH)(lit.)
Storage Condition	Sealed in dry,Room Temperature
Refractive Index	1.76
MDL	MFCD04222155

α-ADN - Risk and Safety

HS Code

29029090

α-ADN - Introduction

9,10-di (1-naphthyl)anthracene (9,10-di (1-naphthyl)anthracene) is an organic compound with the chemical formula C34H22. Its appearance is white to light yellow powdery crystals with aromatic taste. The following is a description of the properties, uses, preparation and safety information of the compound:

Nature:
1. Melting Point: 248-252 ° C
2. Boiling Point: no public data
3. Soluble in non-polar solvents, such as chloroform, dichloromethane and benzene, but almost insoluble in water
4. Can emit blue and green light under ultraviolet light
5. Good thermal stability

Uses: 9,10-di (1-napthyl) anthracene is an organic light-emitting material. Due to its unique photoelectric properties, it can be used in organic light-emitting diodes (OLED), organic solar cells and fluorescent probes.

Preparation method: 9,10-di (1-naphthyl)anthracene can be synthesized by naphthyl alkylation reaction. The specific preparation method is as follows: 1-naphthyl halogenated hydrocarbon (such as 1-bromonaphthalene) is reacted with 1-naphthyl sodium azide to generate 1,1 '-bis (1-naphthyl)-2,2'-biphenyl compounds. This was then subjected to a condensation reaction under acidic conditions to give the target product 9,10-di (1-napthyl) anthracene.

Safety information: 9,10-di (1-napthyl) anthracene has low toxicity and harmfulness, but the following matters still need to be paid attention:
1. Avoid contact with skin, eyes and respiratory tract, and wear personal protective equipment when using.
2. May be harmful to the water environment, do not discharge it into the water source.
3. If the compound is accidentally inhaled or ingested, seek medical attention immediately.
4. In storage and handling, please follow the safety procedures.

Last Update：2024-04-10 22:29:15