Interesting facts
Interesting Facts about 4-(m-tolylazo)aniline
4-(m-tolylazo)aniline, also known as a coupling agent in dye manufacturing, garners interest for its applications in various fields of chemistry and industrial processes. Here are some captivating insights about this compound:
- Dye Chemistry: This compound plays a crucial role as an intermediate in the production of azo dyes. Azo dyes are notable for their vibrant colors and are widely used in textiles and other materials.
- Coupling Reaction: It participates in coupling reactions, combining with diazonium salts to form colorimetric products. This property is essential in analytical chemistry, particularly in colorimetric assays.
- Biological Activity: Some studies suggest potential biological activities of this compound, which may open avenues for research in pharmacology and biochemistry.
- Electron Donor: As an aromatic amine, 4-(m-tolylazo)aniline functions effectively as an electron donor in various chemical reactions. This aptitude is vital for developing electronic materials.
- Research Interest: Ongoing research is exploring its environmental effects, especially related to its degradation products, as the presence of azo compounds in nature can often lead to ecological concerns.
As the world of chemistry evolves, compounds like 4-(m-tolylazo)aniline continue to excite both students and professionals alike. In the words of chemist Robert H. Grubbs, "The best way to predict the future is to invent it." This sentiment captures the essence of how such compounds could influence future innovations in materials science and beyond.
Synonyms
722-23-6
4-[2-(3-Methylphenyl)diazenyl]benzenamine
4-(2-(3-Methylphenyl)diazenyl)benzenamine
3'-Methyl-4-aminoazobenzene
BRN 0642988
4-((3-Methylphenyl)azo)benzenamine
ANILINE, p-(3-METHYLPHENYLAZO)-
NoName_3886
4-amino-3'-methylazobenzene
CHEMBL84050
SCHEMBL9114273
azobenzene, 4-amino-3'-methyl-
DTXSID50903254
KCOITMFSLVDOGO-UHFFFAOYSA-N
DTXSID001269996
Solubility of 4-(m-tolylazo)aniline
4-(m-tolylazo)aniline, a compound with the chemical formula C13H12N4, exhibits interesting solubility characteristics that are influenced by its structure. This compound is generally recognized for its moderate to low solubility in water, which can be attributed to several factors:
In general, 4-(m-tolylazo)aniline is expected to have better solubility in organic solvents such as ethanol or acetone, rather than in aqueous solutions. This is due to the hydrophobic interactions dominating in non-polar environments.
In summary, the solubility of 4-(m-tolylazo)aniline is a dynamic property influenced by its functional groups, molecular interactions, and environmental conditions. Understanding these aspects is crucial for applications in chemical synthesis and analytical procedures.