Disperse Orange 25
- Molecular formula
- C14H14ClN3
- CAS Number
- 3179-89-3
- IUPAC Name
- 4-(3-chlorophenyl)azo-N,N-dimethyl-aniline
- Molecular Weight
- 268.74g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.1800g/cm3
- Synonyms
- 4-(3-CHLOROPHENYLAZO)-N, N-DIMETHYLANILINE
Identification
Interesting Facts About 4-(3-Chlorophenyl)azo-N,N-dimethyl-aniline
4-(3-Chlorophenyl)azo-N,N-dimethyl-aniline is a fascinating compound primarily known for its role in the dye industry. Here are some intriguing aspects of this compound:
- Azo Dye Significance: As an azo compound, it features the characteristic -N=N- linkage, which is integral in the formation of vibrant dyes. Azo dyes are notorious for their vivid colors and wide utilization in textiles.
- Color Properties: The compound is often recognized for its rich hues, which can range from yellow to red based on environmental factors and interactions with other substances.
- Industrial Application: It is widely employed in coloring fabrics, paper, and even plastics, showcasing its versatility as a synthetic dye.
- Environmental Impact: While azo dyes provide brilliant coloration, some can be harmful; hence, research is ongoing to assess the biodegradability and safety of these compounds in the environment.
- Synthetic Pathways: Synthesizing Azo dyes typically involves coupling diazonium salts with aromatic compounds, a process that underscores key principles in organic chemistry.
Moreover, the compound is a remarkable example of how molecular structure influences properties and reactions in chemical systems. Its studies lead to a deeper understanding of azo compounds in general, paving the way for safer and more sustainable practices in the dye industry.
As researchers continue to explore the capabilities of compounds like 4-(3-Chlorophenyl)azo-N,N-dimethyl-aniline, the fields of organic synthesis and material science keep expanding, providing exciting opportunities for innovation and growth.