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2,2'-Thiodiethanol

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Identification
Molecular formula
C4H10O2S3
CAS number
123-00-2
IUPAC name
2-(2-hydroxyethyltrisulfanyl)ethanol
State
State

2,2'-Thiodiethanol is typically in a liquid state at room temperature.

Melting point (Celsius)
-9.00
Melting point (Kelvin)
264.15
Boiling point (Celsius)
222.00
Boiling point (Kelvin)
495.15
General information
Molecular weight
154.25g/mol
Molar mass
154.2540g/mol
Density
1.2550g/cm3
Appearence

2,2'-Thiodiethanol appears as a colorless or pale yellow liquid. It is hygroscopic in nature and has a characteristic odor.

Comment on solubility

Solubility of 2-(2-hydroxyethyltrisulfanyl)ethanol

The solubility of 2-(2-hydroxyethyltrisulfanyl)ethanol, a compound featuring a distinctive trisulfanyl group, is influenced by several factors that contribute to its overall behavior in various solvents. Here are the key aspects to consider:

  • Polarity: Due to the presence of multiple -OH (hydroxyl) groups in its structure, this compound is likely to exhibit good solubility in polar solvents such as water and alcohols, enhancing its ability to form hydrogen bonds.
  • Hydrophobic Interactions: The trisulfanyl moiety may introduce some hydrophobic characteristics, which can decrease solubility in predominantly polar solvents, yet may enhance solubility in certain organic solvents.
  • Temperature Dependence: The solubility may vary with temperature, often increasing at elevated temperatures, making it beneficial to explore solubility at different thermal conditions.
  • pH Sensitivity: Changes in pH can significantly affect the ionization state of the compound, further influencing its solubility in aqueous environments.

Overall, the solubility behavior of 2-(2-hydroxyethyltrisulfanyl)ethanol may be characterized as multi-faceted and context-dependent, making it an intriguing subject for further investigative studies.

Interesting facts

Interesting Facts about 2-(2-hydroxyethyltrisulfanyl)ethanol

2-(2-hydroxyethyltrisulfanyl)ethanol is a fascinating compound with unique properties and applications in various fields. Here are some intriguing aspects that highlight its scientific significance:

  • Structural Composition: The compound contains a trisulfanyl group, which is unusual and provides interesting reactivity compared to similar aliphatic alcohols. The presence of three sulfur atoms introduces unique functional characteristics to the molecule.
  • Biochemical Applications: Due to its multifunctional nature, 2-(2-hydroxyethyltrisulfanyl)ethanol is explored for potential applications in the synthesis of biomolecules. It can serve as a building block in organic synthesis or in the development of pharmaceuticals.
  • Thiol Functionality: The compound exhibits thiol behavior due to the sulfur atoms, making it valuable for studying reactions involving nucleophiles and electrophiles. This can lead to the development of new chemical pathways in synthetic chemistry.
  • Medicinal Interest: The compound is gaining attention in medicinal chemistry for its potential antioxidant properties, which can mitigate oxidative stress in biological systems. This suggests potential therapeutic applications in diseases linked to oxidative damage.
  • Research Implications: Scientists are also investigating the interactions of this compound with various biological macromolecules, which can provide insights into cellular mechanisms and signaling pathways influenced by thiol groups.

In summary, 2-(2-hydroxyethyltrisulfanyl)ethanol exemplifies how modifications to conventional structures can produce compounds with innovative properties. As research continues, it's likely that the applications of this compound will expand across multiple disciplines, showcasing the ever-evolving landscape of chemical science.

Synonyms
2,2'-Trithiobisethanol
Bis(2-hydroxyethyl)trisulfide
4428-14-2
Antibiotic BS 1
Bis(2-hydroxyethyl) trisulfide
2-(2-hydroxyethyltrisulfanyl)ethanol
ETHANOL, 2,2'-TRITHIOBIS-
BS 1
ZU2OG5OJW7
NSC-127171
NSC 127171
BRN 1740589
Ethanol,2'-trithiobis-
UNII-ZU2OG5OJW7
Di(2-hydroxyethyl)trisulfide
3-01-00-02128 (Beilstein Handbook Reference)
SCHEMBL2108625
DTXSID10196100
CHEBI:207950
PSTIDNOIODJAFC-UHFFFAOYSA-N
2,2'-TRITHIOBIS(ETHANOL)
2-(2-hydroxyethyltrisulanyl)ethanol
ETHANOL, 2,2'-TRITHIODI-
NSC127171
AKOS006276524
BS 1, FROM BACILLUS STEAROTHERMOPHILUS