9,10-Anthracenedione, 1,4,5,8-tetrakis[(4-butylphenyl)amino]- - Names and Identifiers
Name | 9,10-Anthracenedione, 1,4,5,8-tetrakis[(4-butylphenyl)amino]-
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Synonyms | 9,10-Anthracenedione, 1,4,5,8-tetrakis[(4-butylphenyl)amino]- 1,4,5,8-tetrakis(4-butylanilino)anthracene-9,10-dione TBPAAQ
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CAS | 108313-21-9
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EINECS | 445-710-5 |
9,10-Anthracenedione, 1,4,5,8-tetrakis[(4-butylphenyl)amino]- - Physico-chemical Properties
Molecular Formula | C54H60N4O2
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Molar Mass | 797.0798 |
Density | 108313-21-9.gif |
9,10-Anthracenedione, 1,4,5,8-tetrakis[(4-butylphenyl)amino]- - Introduction
The 9,10-anthraquinone, 1,4, 5,8-tetrakis (4-butylphenyl) amino compound is an organic compound with the chemical formula C50H44N4O2. It is a yellow crystalline solid.
The following are the properties of the compound:
1. Appearance: yellow crystal solid
2. Melting Point: about 285-290 ℃
3. Solubility: high solubility in common organic solvents
The compounds are used:
1. Dye: Because of its strong pigment characteristics, it is widely used in the field of dyes, especially for dye-sensitized solar cells.
2. Photosensitizer: as a photosensitizer, it can be used for photosensitive materials, fluorescent dyes and organic optoelectronic devices.
3. Electronic devices: Due to its excellent electrical and optical properties, the compound can also be used in the preparation of organic electronic devices, such as organic field-effect transistors and organic photodiodes.
Regarding the preparation method, the following is a commonly used synthetic route:
1. Add 9,10-anthracene functional compound and excess 4-butylaniline to a reaction vessel.
2. Reaction for a period of time under mild reaction conditions usually requires a longer reaction time and appropriate solvents.
3. After the reaction, the product is obtained by crystallization or other purification methods.
When using and handling 9,10-anthraquinone, 1,4,5,8-Tetra (4-butylphenyl) amino compounds, the following safety information should be noted:
1. Avoid inhalation or contact with skin and eyes. Appropriate personal protective equipment, such as gloves, protective glasses and laboratory coats, should be worn during operation.
2. In the laboratory operation and storage, should maintain a well-ventilated environment.
3. Do not contact the compound with strong oxidants and flammable substances to avoid dangerous reactions.
4. The compound should be stored in a dry, low-temperature, dark environment, away from fire and flammable substances.
Last Update:2024-04-10 22:29:15