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8-[(3,5-dinitrobenzoyl)amino]naphthalene-1,3,5-trisulfonic acid

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Identification
Molecular formula
C17H10N3O12S3
CAS number
121-30-2
IUPAC name
8-[(3,5-dinitrobenzoyl)amino]naphthalene-1,3,5-trisulfonic acid
State
State

This compound is typically solid at room temperature. Its crystalline structure gives it a distinct appearance suited for various applications in industrial and research settings.

Melting point (Celsius)
160.00
Melting point (Kelvin)
433.15
Boiling point (Celsius)
240.00
Boiling point (Kelvin)
513.15
General information
Molecular weight
522.43g/mol
Molar mass
522.4300g/mol
Density
2.0100g/cm3
Appearence

This compound typically appears as a yellow to orange crystalline solid. It may also be observed as a powder with a similar color range. The intensity of its color is due to the presence of nitro groups in the aromatic ring.

Comment on solubility

Solubility of 8-[(3,5-dinitrobenzoyl)amino]naphthalene-1,3,5-trisulfonic acid

8-[(3,5-dinitrobenzoyl)amino]naphthalene-1,3,5-trisulfonic acid (C17H10N3O12S3) exhibits intriguing solubility properties that warrant exploration. Generally, the solubility of this compound can be influenced by several factors:

  • Solvent Polarity: The presence of multiple sulfonic acid groups enhances solubility in polar solvents, particularly water, while reducing solubility in nonpolar solvents.
  • pH of the Solution: Since it contains acidic functional groups, solubility will often increase in alkaline conditions where the acid can deprotonate, providing a more soluble anionic form.
  • Temperature Effects: Like many organic compounds, solubility may increase with temperature, making it important to consider operational temperatures during practical applications.

The presence of the dinitrobenzoyl functional group also affects the solubility dynamics, as it can participate in specific interactions with solvent molecules. As a general rule, compounds with more polar functional groups tend to have improved solubility in polar media. Therefore, understanding the solubility behavior of this compound is crucial when considering its applications in various fields, from pharmaceuticals to analytical chemistry.

In conclusion, the solubility of 8-[(3,5-dinitrobenzoyl)amino]naphthalene-1,3,5-trisulfonic acid is subject to the interplay of its chemical structure and environmental conditions, making it a compound of interest for deeper solubility studies.

Interesting facts

Interesting Facts About 8-[(3,5-Dinitrobenzoyl)amino]naphthalene-1,3,5-trisulfonic Acid

8-[(3,5-Dinitrobenzoyl)amino]naphthalene-1,3,5-trisulfonic acid is a fascinating compound that draws attention for its unique structure and applications. Here are some intriguing aspects of this chemical:

  • Complex Structure: The compound features a naphthalene core, which is notable for its aromatic properties and ability to engage in electrophilic substitutions.
  • Functional Groups: It contains multiple functional groups including sulfonic acid groups, which enhance its water solubility and reactivity.
  • Applications: This compound is often utilized in the fields of organic synthesis and materials science, contributing to the development of dyes and fluorescent markers.
  • Biological Activity: Compounds like this one may exhibit antimicrobial and antiviral properties, making them of interest in pharmaceuticals and biochemistry.
  • Investigative Uses: Its unique functionalization allows researchers to study interactions with biological systems, impacting drug delivery mechanisms or targeting specific biochemical pathways.

As a scientist or student exploring this compound, one might find it exciting to note that its complexity allows for diverse applications. The integration of nitro groups enhances reactivity, while the sulfonic acid moieties provide essential solubility characteristics needed for biological applications. The intricate balance of structure and function exemplifies the beauty of organic chemistry, where a single compound can pave the way for advancements in multiple scientific disciplines.

In summary, 8-[(3,5-Dinitrobenzoyl)amino]naphthalene-1,3,5-trisulfonic acid is more than just a chemical formula; it is a compound rich with potential and a subject of ongoing research. As aptly stated, "Chemistry is the central science," and compounds like this are perfect examples of how chemical innovation leads to breakthroughs across various fields.