Interesting facts
Interesting Facts about 3-Aminonaphthalene-1,5-disulfonic Acid
3-Aminonaphthalene-1,5-disulfonic acid, commonly referred to in the scientific community as a key sulfonic acid derivative, offers a fascinating perspective on the versatility and utility of aromatic compounds. As a member of the naphthalene family, this compound presents a range of interesting properties and applications:
- Versatile Applications: This compound is primarily utilized in the dye manufacturing industry, serving as an important coupling agent for azo dyes. Its ability to aid in the formation of colored compounds highlights the significance of sulfonic acids in color chemistry.
- Structural Insight: The presence of both amino and sulfonic functional groups makes this compound unique. The amino group enhances its reactivity, while the sulfonic groups increase its solubility in water, making it a valuable intermediate in organic synthesis.
- Biological Significance: Compounds like 3-aminonaphthalene-1,5-disulfonic acid can also help in various biological studies. Its ability to act as a fluorescent probe allows for applications in biochemical research and diagnostic procedures.
- Environmental Awareness: The synthesis and use of this compound raise important discussions about environmental chemistry, particularly the management of waste substances derived from industrial production processes.
- Advanced Research: Ongoing studies focus on exploring the potential pharmaceutical properties of this compound. Its structural features might give rise to new derivatives with enhanced biological activity.
In conclusion, 3-aminonaphthalene-1,5-disulfonic acid showcases the interconnectedness of chemical structure and properties, demonstrating how even simple modifications can lead to significant changes in application and functionality. As scientists continue to explore the depths of chemical compounds, this compound stands out as an exemplary subject for further investigation and innovation.
Synonyms
131-27-1
3-aminonaphthalene-1,5-disulfonic acid
2-Amino-4,8-naphthalenedisulfonic acid
C acid
1,5-Naphthalenedisulfonic acid, 3-amino-
3-Aminonaphthalene-1,5-disulphonic acid
Acid IV
2-Naphthylamine-4,8-disulfonic acid
3-Amino-1,5-naphthalenedisulfonic acid
Kyselina C [Czech]
Kyselina C
4,8-Disulfo-2-naphthalamine
7-Amino-1,5-naphthalenedisulfonic acid
beta-Naphthylaminedisulfonic acid
NSC 7558
EINECS 205-020-5
X5M28DHP3K
4,8-Disulfo-2-naphthylamine
Kyselina 2-naftylamin-4,8-disulfonova
beta-Naphthylamine-4,8-disulfonic acid
BRN 3104699
NSC-7558
Kyselina 2-naftylamin-4,8-disulfonova [Czech]
.beta.-Naphthylamine-4,8-disulfonic acid
DTXSID5059616
3-aminonaphthalene-1,5-disulfonicacid
UNII-X5M28DHP3K
SCHEMBL147723
Aminonaphthalene disulfonic acid
DTXCID6034007
NSC7558
WLN: L66J BSWQ DZ GSWQ
.beta.-Naphthylaminedisulfonic acid
MFCD00035722
STL426739
AKOS015900218
FA40997
2-aminonaphthalene-4,8-disulphonic acid
3-aminonaph-thalene-1,5-disulfonic acid
3-aminonaphthalene-1,5-di-sulfonic acid
AC-11137
NS00002529
205-020-5
Solubility Characteristics of 3-Aminonaphthalene-1,5-disulfonic Acid
3-Aminonaphthalene-1,5-disulfonic acid, with the chemical formula C10H9O6S2N, exhibits distinctive solubility properties that are important for its applications in various fields.
This compound is known to be highly soluble in water, enabling it to readily dissociate into its constituent ions. The solubility can be explained by the presence of sulfonic acid groups, which are strong acids and significantly enhance the compound's ability to interact with water molecules. Here are some key points regarding its solubility:
Furthermore, 3-aminonaphthalene-1,5-disulfonic acid is known to be less soluble in organic solvents, which is typical for compounds with strong polar functional groups. As a result, it is essential to consider the solvent environment when utilizing this compound in research and industrial processes.
In summary, the solubility of 3-aminonaphthalene-1,5-disulfonic acid in water plays a crucial role in its functionality and effectiveness in numerous applications. Its high solubility enhances its utility in various chemical processes.