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bis(ethylthio)methanethione

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Identification
Molecular formula
C5H10S3
CAS number
21099-30-5
IUPAC name
bis(ethylsulfanyl)methanethione
State
State

At room temperature, bis(ethylthio)methanethione is in a liquid state.

Melting point (Celsius)
-22.00
Melting point (Kelvin)
251.15
Boiling point (Celsius)
195.00
Boiling point (Kelvin)
468.15
General information
Molecular weight
150.28g/mol
Molar mass
150.2840g/mol
Density
1.0630g/cm3
Appearence

Bis(ethylthio)methanethione appears as a pale yellow liquid. It is a compound known for its characteristic thioether odor, which resembles that of organosulfur compounds. The liquid is typically clear and free-flowing under standard conditions.

Comment on solubility

Solubility of bis(ethylsulfanyl)methanethione

Bis(ethylsulfanyl)methanethione, a compound with the formula C6H14S2, exhibits specific solubility characteristics that are important for its applications and behavior in various environments.

Key Points about Solubility:

  • Due to the presence of the ethylsulfanyl groups, this compound displays notable solubility in organic solvents such as ethanol and acetone.
  • It shows limited solubility in water, primarily because of the hydrophobic nature of the ethyl groups.
  • The solubility profile can be influenced by factors such as temperature and the presence of specific ions that may interact with the molecule.

In environments where polar solvents are predominant, this may lead to a low dissolution rate, making it essential to consider alternative solvents for dissolution. As quoted in many studies, "the solubility of a compound is a key factor influencing its chemical reactivity and biological interactions." Thus, understanding the solubility behavior of bis(ethylsulfanyl)methanethione is essential for effective applications in synthetic and industrial processes.

Interesting facts

Interesting Facts about bis(ethylsulfanyl)methanethione

bis(ethylsulfanyl)methanethione is a fascinating compound that falls into the category of organosulfur compounds. Here are some intriguing aspects to consider:

  • Structure & Tautomerism: This compound exhibits a unique structure that includes two ethylsulfanyl groups attached to a methanethione core. Its structural versatility allows it to participate in various tautomeric forms, which can significantly influence its chemical behavior.
  • Reactivity: Given its sulfur content, bis(ethylsulfanyl)methanethione can be quite reactive, especially in nucleophilic substitution reactions. This property makes it an interesting target for synthetic chemists looking to develop new sulfur-containing compounds.
  • Biological Potential: Research indicates that organosulfur compounds can exhibit antimicrobial properties. Compounds like bis(ethylsulfanyl)methanethione are being explored for their potential in pharmacology, potentially leading to new antibacterial or antifungal agents.
  • Odoriferous Nature: Compounds in this category are often characterized by strong, sometimes unpleasant odors. This aspect makes them useful in the study of olfaction and sensory responses in both humans and animals.
  • Industrial Applications: The compound has potential uses in the development of agrochemicals, particularly as a pesticide. Its reactive nature may lend itself to various formulations aimed at pest control.

In summary, bis(ethylsulfanyl)methanethione is more than just a chemical entity; it plays a significant role in the exploration of organic synthesis, biological applications, and potential industrial uses. As the field of chemistry advances, this compound and others like it may pave the way for innovative solutions in health, agriculture, and materials science.

Synonyms
Diethyl trithiocarbonate
2314-49-0
Carbonotrithioic acid, diethyl ester
CARBONIC ACID, TRITHIO-, DIETHYL ESTER
bis(ethylsulfanyl)methanethione
EINECS 219-012-4
BRN 1745274
SCHEMBL35180
bis(ethylsulfanyl)-methanethione
DTXSID50177711
Trithiocarbonic acid, diethyl ester
AKOS006278479
NS00048016