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1,4,5,8-Tetrakis(phenylamino)anthraquinone (CAS No. 66181-84-8) is a highly conjugated anthraquinone derivative widely used in advanced organic electronic and functional dye applications. Its multiple phenylamino substituents significantly enhance electron-donating capability and π–π interaction, enabling strong light absorption and charge-transfer properties, which make it a valuable intermediate for high-performance optoelectronic materials and specialty pigments.
Contact us for more information: selina@coreychem.com
| Product Name | 1,4,5,8-tetrakis(phenylamino)anthraquinone |
| Synonyms | 1,4,5,8-tetrakis(phenylamino)anthraquinone;1,4,5,8-Tetraanilino-9,10-anthraquinone;1,4,5,8-Tetrakis(phenylamino)-9,10-anthracenedione;1,4,5,8-Tetraanilino-9,Chemicalbook10-anthracenedione;9,10-Anthracenedione,1,4,5,8-tetrakis(phenylamino)-;Einecs266-223-2;1,4,5,8-tetraanilinoanthracene-9,10-dione;C.I.SolventBlue146:C.I.645080 |
| CAS NO | 66181-84-8 |
| Purity | 98% |
| EINECS No. | 266-223-2 |
| MF | C38H28N4O2 |
| MW | 572.65 |
| Contact | selina@coreychem.com |
1,4,5,8-Tetrakis(phenylamino)anthraquinone (CAS No. 66181-84-8) is a highly conjugated anthraquinone derivative featuring four electron-donating phenylamino groups symmetrically substituted on the quinone core. This donor–acceptor architecture provides strong intramolecular charge-transfer characteristics, broad visible-light absorption, and excellent thermal stability, making it a valuable functional material in advanced optoelectronics, specialty dyes, and molecular electronics research. Its specific applications are as follows:
Electronic Structure Advantage:
The anthraquinone core acts as an electron-accepting unit, while the phenylamino substituents serve as electron donors, forming a typical D–A (donor–acceptor) system.
Applications:
Organic semiconductors for research in OFETs (organic field-effect transistors)
Functional component in OLED charge-transport or emissive layers
Active material in organic photovoltaic (OPV) studies
Effect:
Enhances light absorption, charge mobility, and molecular packing stability in π-conjugated systems.
Structural Function:
The extended π-conjugation and strong electron-donating groups intensify visible-light absorption and tunable coloration.
Applications:
High-performance organic dyes
Functional pigments for specialty coatings and plastics
Research in near-infrared or deep-color chromophores
Effect:
Provides strong coloration, improved photostability, and thermal resistance compared with simple anthraquinone derivatives.
Reactivity:
The amine groups allow further functionalization through acylation, alkylation, or cross-coupling reactions, enabling structural tuning.
Applications:
Construction of conjugated polymers
Design of donor–acceptor macromolecules
Development of molecular switches or photoresponsive systems
Effect:
Improves electronic tunability, structural rigidity, and long-term material stability.
Stability:
Generally exhibits good thermal stability due to its rigid aromatic framework, but protection from strong oxidizing environments is recommended.
Usage Scope:
Primarily utilized in research-scale material science and electronic material development rather than bulk commodity production.
The core value of 1,4,5,8-Tetrakis(phenylamino)anthraquinone lies in its strongly conjugated donor–acceptor structure, which enables efficient charge transfer and broad optical activity. It serves as a versatile building block in advanced organic electronic materials, functional dyes, and molecular engineering research, with significant potential in next-generation optoelectronic systems.
Packaging information: 1KG; 25KG; 100KG
