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2-Ethylthioethanethiol

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Identification
Molecular formula
C4H10S2
CAS number
38275-53-9
IUPAC name
2-ethylsulfanylethanethiol
State
State

At room temperature, 2-ethylsulfanylethanethiol is a liquid. It is relatively volatile, and its pungent odor may be noticeable even in small quantities. The liquid's low melting point ensures that it remains in a liquid state under standard laboratory conditions.

Melting point (Celsius)
-50.00
Melting point (Kelvin)
223.15
Boiling point (Celsius)
173.00
Boiling point (Kelvin)
446.15
General information
Molecular weight
122.24g/mol
Molar mass
122.2400g/mol
Density
0.9526g/cm3
Appearence

2-Ethylsulfanylethanethiol is a colorless to pale yellow liquid. It possesses a strong, unpleasant odor, similar to that of other thiol-containing compounds, often described as skunky or rotten. The liquid is clear and can form a thin film on surfaces.

Comment on solubility

Solubility of 2-Ethylsulfanylethanethiol

2-Ethylsulfanylethanethiol, with its unique molecular structure, exhibits intriguing solubility characteristics. This compound is generally soluble in organic solvents while exhibiting limited solubility in water. Understanding its solubility can be broken down into several key points:

  • Polar and Non-polar Solvents: The compound tends to dissolve well in non-polar solvents due to its hydrophobic ethyl group, making it favorable for use in organic reactions.
  • Water Solubility: The limited solubility in water arises from its molecular structure, which contains non-polar regions that repel water molecules.
  • Temperature Effects: Increasing the temperature can enhance solubility in some organic solvents, allowing for higher concentrations in solutions.
  • Functional Group Influence: The presence of the thiol (-SH) group introduces some polar character, enabling limited solubility under specific conditions.

In summary, while 2-ethylsulfanylethanethiol is primarily soluble in organic solvents, its interaction with polar solvents such as water is constrained due to its hydrophobic attributes. This solubility behavior is essential for its applications in various chemical processes where solvent choice is critical.

Interesting facts

Interesting Facts about 2-Ethylsulfanylethanethiol

2-Ethylsulfanylethanethiol, a captivating chemical compound, belongs to the class of thioethers and plays a significant role in various fields. Below are some intriguing aspects of this compound:

  • Structure and Reactivity: This compound features a unique arrangement that includes a sulfur atom connected to both ethyl and ethanethiol groups, which impacts its reactivity and interactions with other chemicals.
  • Odor Properties: Compounds such as 2-ethylsulfanylethanethiol often have characteristic odors. Many sulfur-containing compounds are known for their strong, sometimes unpleasant smells, which can be a crucial aspect in applications such as flavoring in the food industry.
  • Biological Significance: Thioethers are of great interest in the study of biochemistry. They can participate in various biological reactions, and understanding their behavior may lead to insights into metabolic processes.
  • Use in Synthesis: This compound can serve as an important intermediate in organic synthesis, providing a pathway to more complex chemical structures through further reactions.
  • Environmental Impact: Investigations into the safety and environmental impact of sulfur compounds are ongoing. Examining how 2-ethylsulfanylethanethiol interacts with biological systems and the environment can help inform necessary regulations and applications.

In conclusion, 2-ethylsulfanylethanethiol is more than just a chemical formula; it serves as a crucial element in understanding the fascinating world of sulfur compounds, their reactions, and their potential applications in everyday life and industry.

Synonyms
2-Ethylthioethanethiol
26750-44-7
2-(ethylsulfanyl)ethane-1-thiol
Ethanethiol,2-(ethylthio)-
2-ethylsulfanylethanethiol
Ethanethiol, 2-(ethylthio)-
2-(ethylsulfanyl)ethanethiol
2-(ETHYLTHIO)ETHANETHIOL
3-Thia-1-pentanethiol
b-mercaptoethyl ethyl sulfide
SCHEMBL1402296
SCHEMBL1402297
SCHEMBL4482693
SCHEMBL8161659
SCHEMBL12506478
CHEBI:38625
DTXSID70181259
IYQVQZXLTJHEKZ-UHFFFAOYSA-N
AKOS006272807
BS-52527
E85574
EN300-136247
Q27117924
2-Mercaptoethyl ethyl sulfide Silica (PhosphonicS SEM26)