80509-54-2

Basic information

• Product Name: 2,9-Di(cyclododecyl)-anthra2,1,9-def:6,5,10-d'e'f'diisoquinoline-1,3,8,10-tetrone
• Synonyms: 2,9-Di(cyclododecyl)-anthra2,1,9-def:6,5,10-d'e'f'diisoquinoline-1,3,8,10-tetrone
• CAS NO: 80509-54-2
• Molecular Formula: C48H54N2O4
• Molecular Weight: 722.95336
• Product Categories: electronic
• Mol File: 80509-54-2.mol
• Article Data: 2

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2,9-Di(cyclododecyl)-anthra2,1,9-def:6,5,10-d'e'f'diisoquinoline-1,3,8,10-tetrone(CAS DataBase Reference)
• NIST Chemistry Reference: 2,9-Di(cyclododecyl)-anthra2,1,9-def:6,5,10-d'e'f'diisoquinoline-1,3,8,10-tetrone(80509-54-2)
• EPA Substance Registry System: 2,9-Di(cyclododecyl)-anthra2,1,9-def:6,5,10-d'e'f'diisoquinoline-1,3,8,10-tetrone(80509-54-2)

Safety Data

• Hazardous Substances Data: 80509-54-2(Hazardous Substances Data)

Usage

Compound type

Polycyclic aromatic hydrocarbon.

Usage

Commonly used as a charge-transport material in electrophotography and organic light-emitting diodes.

Physical appearance

Yellowish-brown powder.

Melting point

High melting point (specific value not provided in the material).

Solubility

Low solubility in most organic solvents (specific solvents not provided in the material).

Potential application

Studied for its potential as a semiconductor material.

Electron mobility

High electron mobility (specific value not provided in the material).

Thermal stability

Good thermal stability (specific details not provided in the material).

Toxicity

Known to be toxic and carcinogenic, posing health risks to individuals exposed to it.

Safety measures

Proper precautions and safety measures must be taken when handling and using this chemical (specific measures not provided in the material).

Upstream product

• 1502-03-0 Cyclododecylamine 
• 128-69-8 perylene-3,4,9,10-tetracarboxylic acid 3,4:9,10-dianhydride 
• 946-89-4 cyclododecanone oxime 

Relevant articles and documents

Very Soluble and Photostable Perylene Fluorescent Dyes

The synthesis of perylene dyes 2 with two terminal alkyl groups is described.Long-chain alkyl groups do not increase, but diminish solubility.Cycloalkyl substituents give a minimum of solubility with medium sized rings and a maximum with the cyclotetradecyl derivative (2p).Very high solubility in organic solvents is attained by substitution with secondary alkyl residues having two long chains.One of them, the dye with the 1-hexylheptyl substituent (2v), exhibits a solubility of more than 100g/l in most solvents, a fluorescent quantum yield of about 100 percent, and a very high photostability, thus making it suitable for special applications.