Interesting facts
Interesting Facts about N,N-Dimethyl-4-(1-naphthylazo)aniline
N,N-Dimethyl-4-(1-naphthylazo)aniline is a fascinating compound that belongs to the class of azo dyes, which are renowned for their vibrant colors and practical applications. These dyes are synthesized from azo coupling reactions between diazo compounds and activated aromatic systems. Here are some intriguing aspects of this compound:
- Color Properties: Azo compounds like N,N-dimethyl-4-(1-naphthylazo)aniline are characterized by their striking colors, which can range widely depending on the specific structure. This compound is no exception, often presenting vivid hues that make it useful in various dyeing processes.
- Applications: Its unique properties enable this compound to be used in several fields, including:
- Dye Industry: Utilized for coloring textiles and other materials.
- Pharmaceuticals: As a reagent in the development of new drugs.
- Biochemistry: Serving as a marker in certain biological applications.
- Environmental Impact: As with many azo dyes, there are ongoing studies to understand the environmental implications of their use. Some azo compounds may degrade into hazardous substances, prompting the need for responsible management and safer alternatives.
- Synthesis: The preparation of this compound typically involves a diazotization reaction followed by coupling with an aromatic amine. The specifics of the synthesis can inspire deeper discussions on organic reaction mechanisms, making it a popular topic in organic chemistry courses.
As a compound rich in both aesthetic and practical value, N,N-dimethyl-4-(1-naphthylazo)aniline encapsulates the interplay between chemistry and the natural world. Its vibrant color and versatile applications continue to intrigue scientists and students alike, making it a noteworthy subject in the study of organic compounds.
Synonyms
607-59-0
N,N-Dimethyl-4-(2-(1-naphthalenyl)diazenyl)benzenamine
N,N-Dimethyl-4-[2-(1-naphthalenyl)diazenyl]benzenamine
N,N-Dimethyl-4-(1-naphthalenylazo)benzenamine
4-(Dimethylaminobenzeneazo)-1-naphthalene
W4881L86ZF
NSC-4198
CCRIS 983
NSC 4198
ANILINE, N,N-DIMETHYL-p-(1-NAPHTHYLAZO)-
p-Dimethylaminobenzeneazo-1-naphthalene
BRN 0748677
N,N-Dimethyl-p-(1-naphthylazo)-aniline
p-Dimethylaminobenzene-1-azo-1-naphthalene
Benzenamine, N,N-dimethyl-4-(1-naphthalenylazo)-
UNII-W4881L86ZF
NSC4198
RKGIHRYVFSZPKN-UHFFFAOYSA-N
DTXSID401031400
WLN: L66J BNUNR DN1&1
N,n-dimethyl-p-1-naphthylazoaniline
N,N-Dimethyl-p-(1-naphthylazo)aniline
Aniline,N-dimethyl-p-(1-naphthylazo)-
N,N-dimethyl-p-(1-naphthylazo) aniline
p-(Dimethylamino)benzene-azo-1-naphthalene
p-(Dimethylamino)benzene-1-azo-1-naphthalene
Benzenamine,N-dimethyl-4-(1-naphthalenylazo)-
DIMETHYLAMINOBENZENEAZO-1-NAPHTHALENE, 4-
Q27896929
Solubility of N,N-dimethyl-4-(1-naphthylazo)aniline
N,N-dimethyl-4-(1-naphthylazo)aniline, also known by its systematic name, exhibits intriguing solubility characteristics that are essential for its applications in various fields, particularly in dyes and pigments. Understanding its solubility helps in predicting its behavior in different environments.
Some key points to note about the solubility of this compound include:
Researchers often specify that "solubility varies significantly depending on the solvent and temperature," emphasizing the necessity for careful experimentation.
Its solubility profile impacts its use in various applications, making it an essential compound in both academic research and industrial applications.