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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
State
State

At room temperature, the compound is usually in a solid state. It can form either a powdered or crystalline structure.

Melting point (Celsius)
280.00
Melting point (Kelvin)
553.15
Boiling point (Celsius)
0.00
Boiling point (Kelvin)
0.00
General information
Molecular weight
601.36g/mol
Molar mass
601.3630g/mol
Density
1.5000g/cm3
Appearence

Trisodium 8-[(3,5-dinitrobenzoyl)amino]naphthalene-1,3,5-trisulfonate typically appears as a yellow to orange solid. It is a sodium salt of a sulfonated naphthalene derivative, often found as a crystalline powder.

Comment on solubility

Solubility of Trisodium 8-[(3,5-Dinitrobenzoyl)amino]naphthalene-1,3,5-trisulfonate

Trisodium 8-[(3,5-dinitrobenzoyl)amino]naphthalene-1,3,5-trisulfonate (C17H8N3Na3O12S3) exhibits notable solubility characteristics that are important for its applications in various fields, particularly in biochemistry and analytical chemistry.

Solubility Attributes

  • High Water Solubility: This compound is highly soluble in water due to the presence of multiple sulfonate groups, which enhance ionic interactions with polar solvents.
  • Influence of pH: The solubility may vary with changes in pH; typically, a higher solubility is observed in alkaline conditions.
  • Stability in Solution: When dissolved in water, the compound can form stable anionic species that contribute to its reactivity and function in biochemical assays.

The solubility of this compound is a key factor that not only facilitates its use in laboratory settings but also affects its biological availability. It is often described as having **exemplary solubility**, making it a versatile reagent for numerous applications.

In summary, the solubility dynamics of trisodium 8-[(3,5-dinitrobenzoyl)amino]naphthalene-1,3,5-trisulfonate are influenced by its chemical structure and environmental conditions, highlighting the significance of solubility in its practical usage.

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.