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- Molecular formula
- C14H16N3O
- CAS Number
- 12223-33-5
- IUPAC Name
- 4-(4-ethoxyphenyl)azobenzene-1,3-diamine
- Molecular Weight
- 268.32g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.2450g/cm3
- Synonyms
- Ethoxazene
Identification
Interesting facts
Interesting Facts about 4-(4-ethoxyphenyl)azobenzene-1,3-diamine
4-(4-ethoxyphenyl)azobenzene-1,3-diamine is a member of the azo compound family, which is notably recognized for its vivid colors and applications in various fields. Here are some compelling aspects about this fascinating compound:
- Azo Compound Family: As an azo dye, this compound contains the -N=N- functional group. This double bond between nitrogen atoms is crucial as it contributes to the chromophore of the dye, resulting in its intense coloration.
- Applications: It is commonly used in the textile industry for dyeing fabrics, thanks to its ability to produce rich colors. Additionally, its derivatives find uses in the production of inks, plastics, and even in biological studies.
- Biological Activity: Some studies suggest that azo compounds like this can exhibit biological properties, making them of interest in pharmacological research. The interactions within biological systems can shed light on potential therapeutic applications.
- Environmental Concerns: Many azo dyes can decompose into potentially hazardous amines, raising environmental and health concerns. Researchers are actively studying ways to mitigate these effects through greener chemistry practices.
- Synthesis Versatility: The synthesis of this compound can involve various reaction pathways, allowing chemists to explore different methods to achieve the desired structure and properties. This versatility showcases the creativity of synthetic chemists.
In summary, 4-(4-ethoxyphenyl)azobenzene-1,3-diamine is more than just a vibrant dye; it represents a bridge between chemistry and practical applications in daily life, making it a significant subject of study in both academic and industrial settings.