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S-(6-acetylsulfanylhexyl) ethanethioate

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Identification
Molecular formula
C10H20O2S2
CAS number
51741-52-3
IUPAC name
S-(6-acetylsulfanylhexyl) ethanethioate
State
State

In its pure form, the compound exists as a liquid at room temperature. This is due to its lower melting point, which is well below standard room temperature. The compound is typically dispensed in a sealed container to prevent contamination and evaporation.

Melting point (Celsius)
-46.00
Melting point (Kelvin)
227.15
Boiling point (Celsius)
315.20
Boiling point (Kelvin)
588.35
General information
Molecular weight
220.38g/mol
Molar mass
220.3800g/mol
Density
0.9267g/cm3
Appearence

The compound is typically in a liquid state at room temperature and has a clear to pale-yellow color. It has a characteristic odor associated with thioesters.

Comment on solubility

Solubility of S-(6-acetylsulfanylhexyl) ethanethioate

The solubility of S-(6-acetylsulfanylhexyl) ethanethioate can be influenced by various factors including its chemical structure and the solvent used. This compound, characterized by its unique sulfanyl and thioate groups, exhibits distinct solubility properties.

General Solubility Characteristics:

  • Polar Solvents: S-(6-acetylsulfanylhexyl) ethanethioate is likely to have increased solubility in polar solvents such as water due to the presence of functional groups that can engage in hydrogen bonding.
  • Non-Polar Solvents: Conversely, it may show higher solubility in non-polar solvents like hexane, due to hydrophobic interactions arising from its long carbon chain.
  • Temperature Effects: Temperature variations can also influence solubility; typically, an increase in temperature results in greater solubility for many compounds.

As a general guideline, the solubility of organic thioether compounds, like S-(6-acetylsulfanylhexyl) ethanethioate, can vary significantly based on the specific environment:

  1. Identify whether the surrounding medium is polar or non-polar.
  2. Assess the potential for intermolecular interactions, such as dipole-dipole or Van der Waals forces.
  3. Consider the presence of functional groups that can alter solubility dynamics.

In conclusion, the solubility of S-(6-acetylsulfanylhexyl) ethanethioate is a multifaceted property dependent on various chemical interactions and should be evaluated under specific conditions for accurate assessment.

Interesting facts

Interesting Facts about S-(6-acetylsulfanylhexyl) ethanethioate

S-(6-acetylsulfanylhexyl) ethanethioate is a fascinating compound that showcases the intricate world of organic chemistry. This compound, with its unique structure, opens the door to various applications and interests in scientific research.

Key Features:

  • Structural Complexity: The presence of a thioate group alongside a hexyl chain introduces a level of structural diversity that is often explored in the synthesis of new materials.
  • Potential Applications: Compounds like this may be useful in developing flavors or fragrances, as they can interact with olfactory receptors in unique ways.
  • Biochemical Significance: The thioate moiety could suggest potential interactions with biological systems, possibly involved in enzymatic reactions or as signaling molecules.
  • Research Opportunities: The synthesis and study of this compound can provide insights into creating derivatives with enhanced properties for various industrial uses.

In the world of synthetic chemistry, compounds like S-(6-acetylsulfanylhexyl) ethanethioate highlight the potential of harnessing chemical interactions for practical outcomes. As stated by a renowned chemist, “Each compound is a storyteller, revealing secrets of nature through its unique structure and reactivity.”
This compound is no exception and invites chemists to explore its depth.

Further Exploration:

  • Investigating its reactivity with other chemical species.
  • Studying its environmental impact and sustainability.
  • Exploring analogs and their potential in pharmaceutical applications.

With every chemical compound providing a new lens to view the intricacies of both synthetic and biological chemistry, S-(6-acetylsulfanylhexyl) ethanethioate stands out as a promising subject for future studies.

Synonyms
1,6-Hexanedithiol diacetate
SD 4965
1,6-Hexanedithiol, S,S'-diacetate
2678-29-7
BRN 1776159
ACETIC ACID, THIO-, S,S'-HEXAMETHYLENE ESTER
Ethanethioic acid, S,S'-1,6-hexanediyl ester
DTXSID90181291
4-02-00-00553 (Beilstein Handbook Reference)
DTXCID00103782
Ethanethioic acid, S,S'-1,6-hexanediyl ester (9CI)