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Jean's Acid Diiodide

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Identification
Molecular formula
C21H30N2O2S+ 2I-
CAS number
null
IUPAC name
[2-(5-dimethylsulfonio-1H-indol-3-yl)-1-methyl-ethyl]-trimethyl-ammonium;diiodide
State
State

At room temperature, it is typically found in a solid state. This compound is generally stable under standard conditions of temperature and pressure.

Melting point (Celsius)
235.00
Melting point (Kelvin)
508.15
Boiling point (Celsius)
355.00
Boiling point (Kelvin)
628.15
General information
Molecular weight
483.26g/mol
Molar mass
483.2560g/mol
Density
1.7860g/cm3
Appearence

The compound typically appears as an off-white to pale yellow crystalline solid. It may exist as fine powder or crystals, depending on the method of crystallization used. The appearance might slightly vary if impurities are present or due to environmental factors like humidity.

Comment on solubility

Solubility of [2-(5-dimethylsulfonio-1H-indol-3-yl)-1-methyl-ethyl]-trimethyl-ammonium;diiodide

The solubility of the compound [2-(5-dimethylsulfonio-1H-indol-3-yl)-1-methyl-ethyl]-trimethyl-ammonium;diiodide is influenced by several key factors:

  • Nature of the compound: As an ammonium salt, the structure contains quaternary nitrogen, which often enhances solubility in polar solvents.
  • Solvent choice: This compound is expected to be soluble in water and other polar solvents due to its ionic character. The presence of iodide ions may further increase solubility due to their ability to stabilize interactions in aqueous solution.
  • Temperature dependence: Like many compounds, the solubility may increase with temperature. Thus, heating the solution could facilitate the dissolution process.

Furthermore, it’s worth noting that while ionic compounds generally exhibit higher solubility in water, the overall solubility may be affected by concentration and mixing conditions. As a general rule, compounds with higher charge density tend to have increased solubility in polar solvents but may form precipitates at higher concentrations due to saturation effects.

In summary, this compound's solubility is characterized by its ionic nature, solvent compatibility, and temperature effects, making it a fascinating subject for further study in chemical interactions.

Interesting facts

Interesting Facts about [2-(5-dimethylsulfonio-1H-indol-3-yl)-1-methyl-ethyl]-trimethyl-ammonium;diiodide

This fascinating compound, often referred to in the field of organic chemistry, showcases the intriguing intersection between structural complexity and biological activity. Its unique architecture is a testament to the diverse range of chemicals synthesized for various applications. Here are some noteworthy points:

  • Quaternary Ammonium Compound: The presence of a quaternary ammonium group in its structure illustrates its potential as a versatile agent in medicinal chemistry, particularly in drug design.
  • Indole Derivative: As an indole derivative, it may exhibit properties related to biological functions, possibly influencing serotonin receptors, thereby opening avenues for research into neuropharmacology.
  • Dimethylsulfonium Group: The dimethylsulfonio moiety adds an intriguing layer of polarity, which can enhance solubility and conductivity in various environments—a critical feature in ionic liquids.
  • Potential Applications: This compound may be utilized in formulations ranging from biocides to pharmaceutical intermediates, thus making it a valuable candidate for innovation in different scientific fields.
  • Stability and Reactivity: Its diiodide form suggests enhanced stability, a trait that may be exploited for prolonged shelf life in industrial applications.
  • Research Implications: Given its structural characteristics, studies could focus on its interaction with biological molecules, leading to breakthroughs in drug delivery systems or antimicrobial agents.

In conclusion, the compound [2-(5-dimethylsulfonio-1H-indol-3-yl)-1-methyl-ethyl]-trimethyl-ammonium;diiodide stands as a remarkable example of how complex chemical structures can impact functionality, signaling a promising future for further research and application in multiple scientific realms.

Synonyms
5564-14-7
5-Methylthio-3-(2-dimethylaminopropyl)indole dimethyiodide monohydrate
Ammonium, (1-(5-dimethylsulfonio-3-indolyl)-2-propyl)trimethyl-, diiodide, hydrate
DTXSID50970981
Dimethyl{3-[2-(trimethylazaniumyl)propyl]-1H-indol-5-yl}sulfanium diiodide