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N-(4-methylphenyl)diphenylamine CAS:4316-53-4

N-(4-methylphenyl)diphenylamine features a diphenylamine core with a methylphenyl group. Its molecular structure presents potential applications in various fields.

 


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Application and Effect:

N-(4-methylphenyl)diphenylamine exhibits diverse applications owing to its unique chemical structure and properties. One significant use is in the field of organic electronics. It serves as a crucial building block for the synthesis of organic semiconductors utilized in electronic devices such as organic light-emitting diodes (OLEDs), organic photovoltaics (OPVs), and organic field-effect transistors (OFETs). Its conjugated structure facilitates efficient charge transport, making it suitable for incorporation into electronic components, thereby enabling the development of high-performance devices. Furthermore, N-(4-methylphenyl)diphenylamine derivatives are employed in the field of dye-sensitized solar cells (DSSCs). These derivatives function as sensitizers that absorb light and generate electron-hole pairs, initiating the photovoltaic process. By tuning the chemical structure of these derivatives, researchers aim to enhance the light-harvesting efficiency and stability of DSSCs, thereby advancing the development of efficient and cost-effective solar energy conversion technologies. Moreover, N-(4-methylphenyl)diphenylamine and its derivatives find applications in the field of materials science, particularly in the synthesis of functional materials. These compounds serve as precursors for the fabrication of polymers, nanoparticles, and other advanced materials with tailored properties. Their versatile chemical structure allows for the introduction of various functional groups, enabling the engineering of materials with specific optical, electronic, or mechanical characteristics for applications in areas such as coatings, sensors, and optoelectronic devices. Additionally, N-(4-methylphenyl)diphenylamine derivatives have shown promise in the field of chemical sensors and molecular recognition. Functionalized derivatives of this compound can be designed to selectively interact with specific analytes or biomolecules, offering opportunities for the development of sensors for environmental monitoring, medical diagnostics, and food safety. Their ability to undergo diverse chemical reactions enables the fabrication of sensor platforms with high sensitivity and selectivity, contributing to advancements in sensing technology. In summary, the distinctive properties of N-(4-methylphenyl)diphenylamine make it a versatile compound with diverse applications in fields such as organic electronics, photovoltaics, materials science, and chemical sensing. Continued research and development efforts are likely to uncover additional uses and further enhance the utility of this compound and its derivatives in various scientific and technological endeavors.

Product Sample:

L-Arginine1
L-Arginine2

Product Packing:

L-Arginin3

Additional Information:

Composition C19H17N
Assay 99%
Appearance white powder
CAS No.  4316-53-4
Packing Small and bulk
Shelf Life 2 years
Storage Store in cool and dry area
Certification ISO.

 


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