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2-(1H-benzimidazol-3-ium-2-ylsulfanyl)ethyl-diethyl-ammonium dibromide

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Identification
Molecular formula
C15H24Br2N3S
CAS number
2344945-67-8
IUPAC name
2-(1H-benzimidazol-3-ium-2-ylsulfanyl)ethyl-diethyl-ammonium;dibromide
State
State

At room temperature, 2-(1H-benzimidazol-3-ium-2-ylsulfanyl)ethyl-diethyl-ammonium dibromide is in a solid state. This hygroscopic compound should be handled in environments with controlled humidity levels to maintain its stability.

Melting point (Celsius)
205.00
Melting point (Kelvin)
478.15
Boiling point (Celsius)
280.00
Boiling point (Kelvin)
553.15
General information
Molecular weight
406.27g/mol
Molar mass
406.2700g/mol
Density
1.5000g/cm3
Appearence

2-(1H-benzimidazol-3-ium-2-ylsulfanyl)ethyl-diethyl-ammonium dibromide is typically found as a crystalline solid powder. The compound has a white to off-white color and may also appear in a slightly yellowish hue depending on purity and specific formulation. It is hygroscopic, meaning it can absorb moisture from the air, and therefore should be stored in a tightly sealed container and handled with care to avoid clumping due to moisture uptake.

Comment on solubility

Solubility of 2-(1H-benzimidazol-3-ium-2-ylsulfanyl)ethyl-diethyl-ammonium dibromide

The compound 2-(1H-benzimidazol-3-ium-2-ylsulfanyl)ethyl-diethyl-ammonium dibromide is quite interesting in terms of its solubility characteristics. Generally, this compound's solubility can be influenced by a variety of factors, including:

  • Ionization: Being an ammonium salt, it readily dissociates in aqueous solutions, enhancing solubility.
  • Polarity: The presence of both polar (ammonium, bromide) and nonpolar (benzimidazole) components suggests that while it is soluble in water, it can also dissolve in certain organic solvents.
  • Temperature: As is typical for many compounds, solubility may increase with temperature, which is essential to consider when preparing solutions.

In general, salts of quaternary ammonium compounds, like this one, are known for their high solubility in polar solvents, particularly water. As noted in various studies, such compounds often display good solubility when mixed with solutions of slightly acidic or neutral pH due to the balance of ionic interactions.

Moreover, it’s important to recognize that the solubility can also depend on the presence of co-solvents or other ions in the solution. Therefore, when working with 2-(1H-benzimidazol-3-ium-2-ylsulfanyl)ethyl-diethyl-ammonium dibromide, it is recommended to:

  1. Test solubility in both water and organic solvents for practical applications.
  2. Consider using a temperature-controlled environment to determine the maximum solubility.
  3. Use high-purity materials to avoid interference from impurities that might affect solubility.

In conclusion, the solubility of this benzodiazole-based compound appears favorable, particularly in polar solvents, making it a versatile choice for various chemical applications.

Interesting facts

Interesting Facts about 2-(1H-benzimidazol-3-ium-2-ylsulfanyl)ethyl-diethyl-ammonium;dibromide

This compound, with its complex structure, is a fascinating example of how organic and inorganic chemistry can intermingle to create unique properties and functions. Here are some intriguing aspects:

  • Benzimidazole Derivative: The presence of the benzimidazole structure plays a crucial role in the compound's biological activity. Benzimidazoles are known for their diverse pharmacological properties, including antimicrobial and antiparasitic effects.
  • Ammonium Ion: The diethylammonium component indicates that this compound is a quaternary ammonium salt, which is often used for its surfactant properties. These salts are typically known for their ability to act as biocides and antimicrobial agents in various applications.
  • Sulfanyl Group: The inclusion of a sulfanyl (thioether) group adds an interesting dimension. Sulfur-containing compounds are often involved in biochemical processes and can contribute to the overall chemical reactivity and stability of the molecule.
  • Double Bromide Counterion: Being a dibromide suggests enhanced stability of the ionic form, which may influence its solubility and reactivity in various environments. Bromide ions are often less toxic and can improve the compound's compatibility in biological systems.
  • Potential Applications: Due to its structural components, this compound may show promise in pharmaceuticals, particularly in drug development targeting specific pathways in microbial infections or diseases.

As with many compounds in the field of chemistry, the interaction between various functional groups and their resulting properties can lead to innovative applications. This compound exemplifies the beauty of chemical synthesis, where simple elements combine to create substances with profound capabilities.

In the words of chemist Linus Pauling, "Good chemistry is a matter of seeing how the cosmos interacts with its own matter," and this compound certainly reflects that philosophy!

Synonyms
2-(2'-Diethylaminoethylthio)benzimidazoline bromide hydrobromide
18144-28-0
2-((2-(Diethylamino)ethyl)thio)benzimidazole dihydrobromide
BENZIMIDAZOLE, 2-((2-(DIETHYLAMINO)ETHYL)THIO)-, DIHYDROBROMIDE