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2,2,4-Trimethyl-1,3-dithiolane

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Identification
Molecular formula
C6H12S2
CAS number
5910-99-4
IUPAC name
2,2,4-trimethyl-1,3-dithiolane
State
State

At room temperature, 2,2,4-Trimethyl-1,3-dithiolane exists as a liquid. It retains its state under standard laboratory conditions without solidifying or boiling away.

Melting point (Celsius)
-19.00
Melting point (Kelvin)
254.15
Boiling point (Celsius)
184.00
Boiling point (Kelvin)
457.15
General information
Molecular weight
148.27g/mol
Molar mass
148.2710g/mol
Density
0.9700g/cm3
Appearence

2,2,4-Trimethyl-1,3-dithiolane is a colorless liquid, which is characterized by its clear and consistent liquid form. Although typically categorized as colorless, impurities may impart a slight coloration.

Comment on solubility

Solubility of 2,2,4-trimethyl-1,3-dithiolane

2,2,4-trimethyl-1,3-dithiolane is a unique compound with intriguing solubility characteristics. This compound is known to be:

  • Soluble in non-polar solvents: Due to the presence of its dithiolane ring and non-polar alkyl groups, it exhibits good solubility in organic solvents like hexane, ether, and benzene.
  • Practically insoluble in water: The non-polar nature of the compound makes it difficult for 2,2,4-trimethyl-1,3-dithiolane to dissolve in polar solvents such as water. As a rule of thumb, "like dissolves like," and this compound's hydrophobic characteristics prevent solubility in aqueous solutions.
  • Moderately soluble in some alcohols: Depending on conditions, it may show limited solubility in some alcohol-based solvents, though this is not its preferred medium.

Understanding the solubility characteristics of 2,2,4-trimethyl-1,3-dithiolane is essential for its applications and handling in both laboratory and industrial settings. It's crucial to choose the appropriate solvent for the effective utilization of this compound.

Interesting facts

Interesting Facts About 2,2,4-Trimethyl-1,3-dithiolane

2,2,4-trimethyl-1,3-dithiolane is a fascinating compound that belongs to the class of dithiolanes. Known for its unique structure and noteworthy characteristics, this compound has garnered attention in various fields of study. Here are several interesting facts:

  • Structure Highlights: This compound features a six-membered ring containing two sulfur atoms, making it a notable member of the dithiolane family. The presence of multiple methyl groups enhances its stability and steric properties.
  • Natural Occurrences: Dithiolanes, including 2,2,4-trimethyl-1,3-dithiolane, can be found in nature, particularly in certain essential oils. They contribute to the aroma and flavor profiles, making them of interest in the culinary and fragrance industries.
  • Applications in Industry: The compound has potential uses as an intermediate in organic synthesis and may play a role in the formulation of rubber and plastics due to its unique chemical properties.
  • Odor Profile: 2,2,4-trimethyl-1,3-dithiolane is known for having a strong and distinctive odor, often compared to that of garlic. This feature may influence its application as a flavoring agent.
  • Reactivity: The unique structure of this compound allows it to participate in a variety of chemical reactions, making it a valuable subject of study for organic chemists looking to explore sulfur-containing compounds.

As research continues, 2,2,4-trimethyl-1,3-dithiolane may reveal even more intriguing properties and potential applications. The blend of its unique structure, natural occurrence, and industrial applications makes this compound a noteworthy example in the study of organic chemistry.

Synonyms
2,2,4-Trimethyl-1,3-dithiolane
BRN 0102834
1,3-DITHIOLANE, 2,2,4-TRIMETHYL-
DTXSID20974158
5-19-01-00087 (Beilstein Handbook Reference)
DTXCID301401593
crvltuagmfkjea-uhfffaoysa-n
5862-53-3
SCHEMBL10414835
DB-260219