Trisodium 8-[(3,5-dinitrobenzoyl)amino]naphthalene-1,3,5-trisulfonate

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Identification

Molecular formula
C17H8N3Na3O12S3
CAS Number
144026-37-3
IUPAC Name
trisodium;8-[(3,5-dinitrobenzoyl)amino]naphthalene-1,3,5-trisulfonate
Molecular Weight
601.36g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.5000g/cm3
Interesting facts

Interesting Facts about Trisodium 8-[(3,5-Dinitrobenzoyl)amino]naphthalene-1,3,5-trisulfonate

Trisodium 8-[(3,5-dinitrobenzoyl)amino]naphthalene-1,3,5-trisulfonate, often referred to simply as a complex organic sulfonate, is a fascinating compound with a variety of applications and properties:

  • Molecular Structure: This compound exemplifies the rich chemistry of naphthalene derivatives, specifically highlighting the integration of sulfonate groups and nitro functional groups, which contributes to its optical properties.
  • Colorimetric Applications: Due to its vibrant coloration, this compound is frequently utilized in colorimetric analyses, where it acts as a reagent to detect various substances in chemical and biological samples.
  • Environmental Relevance: Compounds with sulfonate groups often demonstrate enhanced water solubility, making them significant in the study of biological processes and environmental chemistry.
  • Biochemical Interactions: The presence of amino and nitro groups suggests potential interactions with biological macromolecules, opening avenues for research into drug delivery systems and biochemical sensors.
  • Research Potential: Scientists are exploring its utility in a range of fields, including materials science for creating dyes and pigments, as well as in medicinal chemistry due to its intriguing structure.

As noted by researchers: “The multifunctionality of these naphthalene derivatives extends their application and enhances our understanding of chemical interactions at the molecular level.”

This compound serves as an excellent example of how intricate organic structures can pave the way for advancements across several scientific domains, from analytical chemistry to environmental science.

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