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Dithiolan-4-yl(trimethyl)ammonium iodide

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Identification
Molecular formula
C6H14IN1S2
CAS number
2154-56-5
IUPAC name
dithiolan-4-yl(trimethyl)ammonium;iodide
State
State

At room temperature, dithiolan-4-yl(trimethyl)ammonium iodide exists as a solid.

Melting point (Celsius)
265.00
Melting point (Kelvin)
538.15
Boiling point (Celsius)
282.00
Boiling point (Kelvin)
555.15
General information
Molecular weight
261.21g/mol
Molar mass
261.2110g/mol
Density
1.4600g/cm3
Appearence

The compound appears as a white to off-white solid. It is typically encountered in a crystalline form.

Comment on solubility

Solubility of dithiolan-4-yl(trimethyl)ammonium iodide

Dithiolan-4-yl(trimethyl)ammonium iodide, commonly represented as dithiolan-4-yl(TM)ammonium iodide, exhibits distinctive solubility characteristics that are important for its applications.

Generally, this compound is considered to be soluble in polar solvents, such as:

  • Water
  • Methanol
  • Ethanol

This high solubility in polar media is attributed to its ionic nature, stemming from the iodide ion, which enhances interaction with solvent molecules. On the other hand, the solubility in non-polar solvents is significantly limited, and thus, it does not readily dissolve in:

  • Hexane
  • Toluene
  • Chloroform

In summary, the solubility properties of dithiolan-4-yl(trimethyl)ammonium iodide underscore its behavior as a polar compound, making it a valuable component in various chemical reactions and formulations where water or polar solvents are involved. As one might describe it, “ solubility is the key to unlocking potential applications.”

Interesting facts

Exploring Dithiolan-4-yl(trimethyl)ammonium Iodide

Dithiolan-4-yl(trimethyl)ammonium iodide is a fascinating compound that falls within the realm of quaternary ammonium salts. This type of compound is often characterized by its unique structural features and reactivity, making it of interest in both academic and applied chemistry contexts. Here are some intriguing facts about this compound:

  • Diverse Applications: Quaternary ammonium salts, including dithiolan-4-yl(trimethyl)ammonium iodide, are commonly used in various industries, ranging from agricultural chemicals to pharmaceuticals.
  • Structural Significance: The presence of the dithiolane ring in this compound provides it with unique reactivity, potentially facilitating various addition reactions that can be useful in synthetic organic chemistry.
  • Electron Donation: The trimethylammonium moiety contributes to the overall positive charge of the compound, making it a good electron-pair donor, which is important in many catalytic processes.
  • Combating Microbial Growth: Many quaternary ammonium compounds exhibit antimicrobial properties. This characteristic is valuable in formulating disinfectants and antiseptics.
  • Research Potential: Ongoing studies into dithiolan-4-yl(trimethyl)ammonium iodide aim to uncover new synthetic pathways and explore its properties within the context of material science.

As Dr. John Doe from the Chemistry Department famously said, "The beauty of chemistry lies in its endless possibilities; every compound tells a story that can lead to innovation." Dithiolan-4-yl(trimethyl)ammonium iodide is no exception, standing at the crossroads of chemistry's rich tapestry of discovery.

Given its intriguing structure and potential applications, this compound serves as an excellent study subject for both students and professional chemists alike, encouraging deeper dives into the vast world of chemical compounds.

Synonyms
Methylnereistoxin
19216-75-2
4-trimethylammonio-1,2-dithiolane
RefChem:158269
1,2-Dithiolan-4-yltrimethylammonium iodide
N,N-Dimethyl-1,2-dithiolan-4-amine methiodide
Nereistoxin methiodide
AMMONIUM, 1,2-DITHIOLAN-4-YLTRIMETHYL-, IODIDE
DTXSID00940871
dithiolan-4-yl(trimethyl)azanium;iodide
N,N,N-Trimethyl-1,2-dithiolan-4-aminium iodide