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1,2,4-Trithiolane

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Identification
Molecular formula
C2H4S3
CAS number
545-46-0
IUPAC name
1,2,4-trithiolane
State
State

1,2,4-Trithiolane is a liquid at room temperature.

Melting point (Celsius)
-15.00
Melting point (Kelvin)
258.15
Boiling point (Celsius)
137.00
Boiling point (Kelvin)
410.15
General information
Molecular weight
124.23g/mol
Molar mass
124.2320g/mol
Density
1.3400g/cm3
Appearence

1,2,4-Trithiolane is a cyclic organic compound and is often found as a colorless liquid. It may also appear as a pale yellow liquid depending on its purity and storage conditions. The compound has a distinct sulfur odor due to the presence of sulfide groups in its ring structure.

Comment on solubility

Solubility of 1,2,4-trithiolane

1,2,4-trithiolane, a sulfur-containing cyclic compound, exhibits unique solubility characteristics that can be interesting to explore. Its solubility can be influenced by several factors:

  • Polarity: 1,2,4-trithiolane possesses polar functional groups due to the presence of sulfur atoms, which can affect its interaction with solvents.
  • Solvent Type: This compound shows better solubility in polar solvents such as water and ethanol, while it may be less soluble in nonpolar solvents like hexane.
  • Temperature: The temperature of the solvent can also impact solubility; typically, higher temperatures increase solubility due to enhanced molecular movement.
  • Concentration: At higher concentrations, 1,2,4-trithiolane might reach a saturation point beyond which it does not dissolve further, forming a heterogeneous mixture.

Overall, the solubility of 1,2,4-trithiolane can be summarized as follows:

  1. Good solubility in polar solvents.
  2. Increased solubility with higher temperatures.
  3. Limited solubility in nonpolar solvents.

“Understanding the solubility of 1,2,4-trithiolane is essential for its application in various chemical processes.”

Interesting facts

Interesting Facts about 1,2,4-Trithiolane

1,2,4-Trithiolane is a fascinating compound that belongs to the class of cyclic thioethers, specifically a member of the thiane family. Its unique structure and properties make it a subject of interest in various fields of chemistry.

Unique Features

  • Structure: The presence of three sulfur atoms within its ring structure greatly influences its chemical behavior and reactivity.
  • Reactivity: 1,2,4-Trithiolane exhibits remarkable reactivity due to the strained ring system, allowing for intriguing reaction pathways.
  • Applications: This compound has garnered attention for use in organic synthesis, catalysis, and as a potential building block in materials science.

Interesting Quotes

Many chemists have noted its versatility, with one stating, "The ability of 1,2,4-trithiolane to participate in diverse chemical reactions opens doors to numerous synthetic applications."

Exploratory Uses

It is also worth mentioning that its derivatives can be utilized in:

  • Pharmaceutical research, showcasing potential in drug synthesis.
  • Environmental studies, where sulfur-containing compounds can influence ecological processes.
  • Materials science for the development of novel polymers and other advanced materials.

The study of 1,2,4-trithiolane not only provides insight into the properties of sulfur-rich compounds but also emphasizes the importance of heterocycles in organic chemistry. Its intriguing characteristics make it a compound worth investigating for both budding chemists and seasoned researchers alike!

Synonyms
1,2,4-TRITHIOLANE
289-16-7
UNII-OF568IX8QZ
1,2,4-Trithiacyclopentane
OF568IX8QZ
DTXSID70183091
SCHEMBL1039752
DTXCID80105582
CHEBI:192387
NS00124667
Q27285625