Interesting facts
              Interesting Facts About 7-Aminonaphthalene-1,3-Disulfonic Acid
7-Aminonaphthalene-1,3-disulfonic acid, often abbreviated as 7-ANDSA, is a fascinating compound that plays a significant role in the field of organic chemistry and dye manufacturing. Here are some intriguing facts about this chemical:
- Versatile Dye Intermediate: This compound is primarily used as an intermediate in the synthesis of various azo dyes, which are known for their vibrant colors and wide applications in textiles, food, and cosmetics.
- Biological Applications: Due to its amino groups and sulfonic acid functionality, 7-ANDSA is utilized in research as a reagent for determining the properties of biological substances and probing biological systems.
- Research Utility: This compound has gained attention in analytical chemistry, as it can be used as a fluorescent probe for studying cellular processes and interactions.
- Synthesis Pathways: Chemists can synthesize 7-aminonaphthalene-1,3-disulfonic acid through various pathways, including nitration and subsequent reduction, showcasing the creativity needed in organic synthesis.
- Environmental Considerations: Due to the increasing concern over environmental pollution, researchers are investigating the biodegradability and environmental impact of its derivatives and related compounds.
As highlighted by chemical researchers, “The exploration of sulfated organic compounds continues to unveil their broader implications in technology and health.” 7-ANDSA exemplifies such potential, opening the door to innovative applications in different scientific fields.
In conclusion, 7-amino-naphthalene-1,3-disulfonic acid stands out as a compound with multifaceted uses and implications, bridging the gap between chemistry and practical applications while inspiring further research and discovery.
Synonyms
          86-65-7
          7-Amino-1,3-naphthalenedisulfonic acid
          7-aminonaphthalene-1,3-disulfonic acid
          Amido-G-acid
          Amino-G-Acid
          1,3-Naphthalenedisulfonic acid, 7-amino-
          Amino-G acid
          2-Amino-6,8-disulfonaphthalene
          2-Aminonaphthalene-6,8-disulfonic acid
          NSC 4013
          2-NAPHTHYLAMINE-6,8-DISULFONIC ACID
          EINECS 201-689-2
          UNII-7C482FX29K
          BRN 2669649
          AI3-28530
          NSC-4013
          AMIDO-G-ACID [MI]
          6,8-disulfo-2-naphthylamine
          DTXSID4058944
          7-Amino-1,3-naphthalenedisulfonic acid, tech.
          7C482FX29K
          6,8-DISULFO-2-AMINONAPHTHALENE
          .beta.-Naphthylamine-6,8-disulfonic acid
          beta-Naphthylamine-6,8-disulfonic acid
          7-Aminonaphthalene-1,3-disulphonic acid
          AminoGAcid
          AminoG acid
          Amino G Acid
          NSC4013
          MFCD00003991
          1, 7-amino-
          7-ANDSA
          7Am-Naphth-1,3diSO3H
          2Amino6,8disulfonaphthalene
          CHEMBL59189
          SCHEMBL151762
          DTXCID9048510
          2Naphthylamine6,8disulfonic acid
          betaNaphthylamine6,8disulfonic acid
          2Aminonaphthalene6,8disulfonic acid
          7Amino1,3naphthalenedisulfonic acid
          7Aminonaphthalene1,3disulphonic acid
          BBL034633
          STL426740
          1,3Naphthalenedisulfonic acid, 7amino
          7-aminonaphthalene-1,3-disulfonicacid
          AKOS015904570
          2-amino-6,8-naphthalenedisulfonic acid
          VS-12624
          NS00039144
          monopotassium 7-amino-1,3-naphthalenedisulfonic acid
          Q21099242
          201-689-2
              
Solubility of 7-Aminonaphthalene-1,3-disulfonic Acid
7-Aminonaphthalene-1,3-disulfonic acid, a sulfonic acid derivative, exhibits a fascinating solubility profile that is influenced by its molecular structure. It is typically highly soluble in water due to the presence of **two sulfonic acid groups** (-SO3H) that confer significant hydrophilicity. Here are some key points to consider regarding its solubility:
In conclusion, the solubility of 7-aminonaphthalene-1,3-disulfonic acid underscores the profound effect that functional groups have on the overall behavior of chemical compounds in solution. It is a prime example of how structural elements dictate solubility characteristics.