Interesting facts
Interesting Facts about N-methyl-4-phenylazo-aniline
N-methyl-4-phenylazo-aniline, commonly known in various scientific circles, is a fascinating compound with multiple applications and properties that intrigue both chemists and industry professionals alike. Here are some notable aspects:
- Dye Applications: This compound is primarily recognized for its role as a dye intermediate. It is often utilized in the production of azo dyes, which are known for their vivid colors and durability, making them popular in the textile and printing industries.
- Structural Characteristics: The presence of both the azo group (–N=N–) and an aniline derivative in its structure lends it unique chemical properties that can be tuned for specific applications, enhancing its versatility.
- Synthesis Insight: The synthesis of N-methyl-4-phenylazo-aniline typically involves methods such as diazotization of an amine followed by coupling reactions. This process is a great way to demonstrate fundamental principles of organic chemistry in a lab setting.
- Potential Health Effects: Like many azo compounds, there are ongoing discussions regarding the safety profile of N-methyl-4-phenylazo-aniline. Some azo dyes are under scrutiny due to potential carcinogenic properties, making safety evaluations crucial in both industrial and academic research contexts.
- Research Applications: Researchers are exploring innovative applications for this compound in fields such as materials science, where it could be used in creating responsive materials or sensors due to its distinct color properties.
In the words of a chemistry professor: "Understanding compounds like N-methyl-4-phenylazo-aniline not only enhances our grasp of chemical interactions but also opens avenues for the development of new materials and dyes that can revolutionize industries."
Overall, N-methyl-4-phenylazo-aniline is an exemplary representative of how chemistry not only shapes our understanding of matter but also impacts various practical applications across different fields.
Synonyms
621-90-9
N-Methyl-4-(2-phenyldiazenyl)benzenamine
4-(Methylamino)azobenzene
p-Monomethylaminoazobenzene
4-Monomethylaminoazobenzene
N-methyl-4-phenyldiazenylaniline
N-Methyl-4-aminoazobenzene
N-Methyl-4-(phenyldiazenyl)aniline
N-Methyl-p-aminoazobenzene
N-Methyl-p-(phenylazo)aniline
Benzenamine, N-methyl-4-(phenylazo)-
ANILINE, N-METHYL-p-(PHENYLAZO)-
MAB
44N974BFDI
p-N-Methylaminoazobenzene
CCRIS 382
N-Methyl-4-(phenylazo)benzenamine
MFCD00059198
4-methylaminoazobenzene
UNII-44N974BFDI
p-(Phenylazo)-N-methylaniline
SCHEMBL5982612
DKOXITJAUZNAPK-FOCLMDBBSA-N
DKOXITJAUZNAPK-UHFFFAOYSA-N
DTXSID201023342
MONOMETHYLAMINOAZOBENZENE, 4-
N-Methyl-4-[phenyldiazenyl]aniline #
N-methyl-N-[4-(phenyldiazenyl)phenyl]amine
M0143
NS00008733
D91285
N-methyl-4-[(E)-2-phenyldiazen-1-yl]aniline
AE-562/43459099
Q27889325
Solubility of N-methyl-4-phenylazo-aniline
N-methyl-4-phenylazo-aniline, with the chemical formula C13H13N3, presents a unique profile regarding its solubility characteristics. Understanding this compound's solubility can help predict its behavior in various chemical environments and applications.
Here are some key points regarding the solubility of N-methyl-4-phenylazo-aniline:
In summary, while N-methyl-4-phenylazo-aniline shows a tendency to dissolve in organic solvents, its solubility in water is typically low. Understanding these nuances is crucial for effectively utilizing this compound in chemical processes.