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Ethyl Violet

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Identification
Molecular formula
C31H42N3O8S
CAS number
2390-59-2
IUPAC name
diethyl-[2-[2-(4-propylphenyl)sulfanyl-3H-benzimidazol-1-ium-1-yl]ethyl]ammonium;2,4,6-trinitrophenolate
State
State

Ethyl Violet is typically found in a solid state at room temperature. Often supplied as a crystalline powder, it is stable under normal conditions and is soluble in water and ethanol, generating a violet-colored solution.

Melting point (Celsius)
146.00
Melting point (Kelvin)
419.15
Boiling point (Celsius)
400.00
Boiling point (Kelvin)
673.00
General information
Molecular weight
678.77g/mol
Molar mass
678.7700g/mol
Density
1.6200g/cm3
Appearence

Ethyl Violet typically appears as a green crystalline powder. It is known for its vibrant violet color when dissolved in an aqueous solution, a characteristic feature utilized in various applications such as biological staining.

Comment on solubility

Solubility of Diethyl-[2-[2-(4-propylphenyl)sulfanyl-3H-benzimidazol-1-ium-1-yl]ethyl]ammonium; 2,4,6-trinitrophenolate

The solubility of this complex compound can be quite intricate, as it combines both organic and ionic components. Generally, the overall solubility may depend on several factors:

  • Structural Characteristics: The presence of sulfonium and ammonium groups suggests that this compound may exhibit ionic behavior, potentially leading to higher solubility in polar solvents.
  • Solvent Interaction: Solubility may be enhanced in polar solvents like water or alcohol due to interactions with the ionic portions of the molecule.
  • Temperature Influence: As with many compounds, increasing the temperature can often increase solubility, particularly for ionic compounds.
  • pH Dependency: The solubility may also be influenced by the pH of the solution, especially given the presence of both amine and anionic components.

Another important consideration is the potential for the compound to form **hydrogen bonds** which could further affect its solubility. Generally, one might summarize its solubility as:

  1. Highly soluble in polar solvents.
  2. Moderate solubility in non-polar solvents due to its hydrophobic organic structure.
  3. Temperature and pH may play significant roles in its solubility profile.

In conclusion, while the compound is expected to show good solubility in polar media, its complete behavior will ultimately depend on the specific conditions of the solution.

Interesting facts

Overview of Diethyl-[2-[2-(4-propylphenyl)sulfanyl-3H-benzimidazol-1-ium-1-yl]ethyl]ammonium; 2,4,6-trinitrophenolate

This fascinating compound, often referred to by the abbreviated name, showcases a blend of intricate structural elements that contribute to its unique properties and potential applications. The combination of a benzimidazolium moiety with a trinitrophenolate anion results in a compound that is not only intriguing from a chemical standpoint but also has significant implications in various fields.

Key Features

  • Multifunctional Structure: The presence of both the benzimidazolium and trinitrophenolate parts allows for a diverse range of interactions and chemical reactivities. This multifunctional design is ideal for exploring various synthetic applications.
  • Biological Relevance: Compounds similar to benzimidazolium salts have been investigated for their potential as antibacterial and antiviral agents. The structural components could lead to promising therapeutic candidates.
  • Unique Electron Dynamics: The trinitrophenolate ion contributes to the electron affinity of the compound, making it interesting for studies related to electron transfer processes and charge transfer complexes.
  • Potential in Material Science: Because of its unique structural features, this compound may be explored for applications in materials science, particularly in the development of novel organic semiconductors.

Research Applications

This compound holds potential in various research areas due to its unique characteristics:

  • Chemical Sensors: Its ability to interact with different ions and molecules can be harnessed for developing sensitive chemical sensors.
  • Pharmaceutical Development: The biological activity associated with similar benzimidazole derivatives makes it a candidate for further medicinal chemistry work.
  • Supramolecular Chemistry: The structural intricacy allows for the study of supramolecular interactions, crucial in creating complex molecular assemblies.

As researchers continue to explore the nuances of this compound, it remains a captivating subject that bridges organic chemistry with applications across biological and material sciences. Indeed, the exploration of diethyl-[2-[2-(4-propylphenyl)sulfanyl-3H-benzimidazol-1-ium-1-yl]ethyl]ammonium; 2,4,6-trinitrophenolate underscores the endless possibilities that chemistry holds in uncovering new materials and therapeutic agents.

Synonyms
1-(2-(Diethylamino)ethyl)-2-((p-propylphenyl)thio)benzimidazole dipicrate
BENZIMIDAZOLE, 1-(2-(DIETHYLAMINO)ETHYL)-2-((p-PROPYLPHENYL)THIO)-, DIPICRATE
4922-03-6