Disperse Orange 3
- Molecular formula
- C17H19N5O2
- CAS Number
- 730-40-5
- IUPAC Name
- N,N-diethyl-4-(4-nitrophenyl)azo-aniline
- Molecular Weight
- 298.34g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.4095g/cm3
- Appearance
- can vary slightly based on particle size and purity, but it generally maintains a consistent orange hue.
- Synonyms
- N, N-Diethyl-4-((4-nitrophenyl)azo)aniline
Identification
Interesting Facts about N,N-diethyl-4-(4-nitrophenyl)azo-aniline
N,N-diethyl-4-(4-nitrophenyl)azo-aniline is a fascinating chemical compound, primarily known for its use in the dye industry. This compound belongs to the class of azo dyes, which are characterized by their vibrant colors and stability, making them essential in various applications.
Here are some intriguing aspects of N,N-diethyl-4-(4-nitrophenyl)azo-aniline:
- Azo Linkage: The azo group (-N=N-) in this compound is what gives it its distinctive color properties. Azo dyes are typically known for their bright hues due to strong light absorption in the visible spectrum.
- Diverse Applications: This compound is utilized in textiles, leather, and paper dyeing, as well as in some food applications. Its stability makes it a favorite for coloring agents.
- Environmental Considerations: Like many azo dyes, there has been significant research into the safety and environmental impacts of N,N-diethyl-4-(4-nitrophenyl)azo-aniline. Some azo dyes can degrade to form potentially harmful aromatic amines, prompting ongoing assessments and regulations.
- Structure and Properties: The presence of diethyl groups contributes to the solubility and stability of the dye, enhancing its color properties compared to other azo compounds.
- Implications in Scientific Research: Beyond its application in dyes, this compound is studied for its potential uses in organic electronics and nanotechnology due to its electronic properties.
According to a recent study, "The integration of azo compounds in layered materials showcases their diverse functionalities beyond traditional dye applications." This highlights the evolving role of compounds like N,N-diethyl-4-(4-nitrophenyl)azo-aniline in modern science.
Overall, N,N-diethyl-4-(4-nitrophenyl)azo-aniline exemplifies the intersection of chemistry, technology, and environmental studies, reinforcing the ongoing dialogue about the benefits and risks associated with chemical compounds in our daily lives.