• 1. Embedding cyclic nitrone in mesoporous silica particles for EPR spin trapping of superoxide and other radicals?
  Eric Besson,Stéphane Gastaldi,Emily Bloch,Selma Aslan,Hakim Karoui,Olivier Ouari,Micael Hardy Analyst, 2019,144, 4194-4203
• 2. Excitable dynamics in the bromate–sulfite–ferrocyanide reaction
  J. Zagora,M. Vosla?,L. Schreiberová,I. Schreiber Phys. Chem. Chem. Phys., 2002,4, 1284-1291
• 3. Excimer emission and magnetoluminescence of radical-based zinc(ii) complexes doped in host crystals?
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• 4. Distinct roles of SNARE-mimicking lipopeptides during initial steps of membrane fusion?
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• Solvents and Organic Chemicals Organic Compounds Benzenoids Naphthalenes Naphthalene sulfonic acids and derivatives Naphthalene sulfonates

Introduction to Sodium 3-amino-5-hydroxy-7-sulfonaphthalene-2-sulfonate (CAS No. 61702-42-9)

Sodium 3-amino-5-hydroxy-7-sulfonaphthalene-2-sulfonate (CAS No. 61702-42-9) is a specialized chemical compound that has garnered significant attention in the field of pharmaceuticals and biotechnology due to its unique structural properties and potential applications. This compound, characterized by its sulfonate and amino functional groups, exhibits remarkable solubility in water and organic solvents, making it a versatile candidate for various biochemical processes.

The molecular structure of Sodium 3-amino-5-hydroxy-7-sulfonaphthalene-2-sulfonate consists of a naphthalene core substituted with amino, hydroxyl, and sulfonate groups. This arrangement imparts a high degree of reactivity, enabling the compound to participate in diverse chemical reactions such as condensation, oxidation, and polymerization. These properties make it particularly useful in the synthesis of complex molecules and in the development of novel drug formulations.

In recent years, there has been a surge in research focusing on the applications of sulfonated aromatic compounds in medicinal chemistry. The presence of multiple sulfonate groups in Sodium 3-amino-5-hydroxy-7-sulfonaphthalene-2-sulfonate enhances its ability to interact with biological targets, making it an attractive candidate for drug development. Specifically, studies have shown that this compound exhibits promising anti-inflammatory and antioxidant properties, which are critical in the treatment of chronic diseases such as arthritis and oxidative stress-related conditions.

The pharmaceutical industry has been exploring the potential of Sodium 3-amino-5-hydroxy-7-sulfonaphthalene-2-sulfonate as a precursor in the synthesis of active pharmaceutical ingredients (APIs). Its ability to form stable complexes with other molecules makes it an excellent candidate for drug delivery systems. Researchers have been investigating its use in creating targeted drug delivery mechanisms that can enhance the efficacy and reduce the side effects of existing medications.

Moreover, the compound's role in material science cannot be overlooked. The sulfonate groups contribute to its ability to act as a surfactant and chelating agent, which are essential properties in various industrial applications. For instance, it has been used in the formulation of detergents, textiles, and paper manufacturing due to its ability to improve water solubility and dispersion of other compounds.

The latest advancements in green chemistry have also highlighted the importance of sustainable chemical synthesis. Sodium 3-amino-5-hydroxy-7-sulfonaphthalene-2-sulfonate fits well into this paradigm as it can be synthesized using environmentally friendly methods that minimize waste and energy consumption. This aligns with global efforts to develop eco-friendly alternatives for traditional chemical processes.

In conclusion, Sodium 3-amino-5-hydroxy-7-sulfonaphthalene-2-sulfonate (CAS No. 61702-42-9) is a multifaceted compound with significant potential across multiple industries. Its unique structural features and reactivity make it invaluable in pharmaceutical research, drug development, material science, and sustainable chemistry. As research continues to uncover new applications for this compound, its importance is only set to grow.

• 5460-09-3(H Acid)
• 6535-70-2(2-Amino-5-hydroxynaphthalene-1,7-disulfonic acid)
• 343321-59-5(8-Amino-1-naphthol-3,6-disulfonic acid monosodium salt)
• 31232-21-0(2,7-Naphthalenedisulfonicacid, 3-amino-4,5-dihydroxy-)
• 16781-08-1(2-Naphthalenesulfonicacid, 6-amino-4-hydroxy-, sodium salt (1:1))
• 312693-54-2(4-AMINO-5-HYDROXY-2 7-NAPHTHALENEDISULF&)
• 3963-80-2(2,7-Naphthalenedisulfonicacid, 4-amino-5-hydroxy-, sodium salt (1:2))
• 489-78-1(8-Amino-4-hydroxynaphthalene-2-sulfonic acid)
• 35439-70-4(1,7-Naphthalenedisulfonicacid, 2-amino-5-hydroxy-, sodium salt (1:2))
• 17265-34-8(2,7-Naphthalenedisulfonicacid, 4-amino-5-hydroxy-, sodium salt (1:?))