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3,6,9-trithiaundecane-1,11-diol

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Identification
Molecular formula
C12H26O2S2
CAS number
54697-61-5
IUPAC name
2-[10-(2-hydroxyethylsulfanyl)decylsulfanyl]ethanol
State
State

At room temperature, it is typically in a liquid state.

Melting point (Celsius)
10.50
Melting point (Kelvin)
283.65
Boiling point (Celsius)
388.85
Boiling point (Kelvin)
661.85
General information
Molecular weight
266.47g/mol
Molar mass
0.0000g/mol
Density
1.0800g/cm3
Appearence

3,6,9-Trithiaundecane-1,11-diol is a colorless liquid that may appear slightly viscous. It has a characteristic odor associated with sulfur-containing compounds.

Comment on solubility

Solubility of 2-[10-(2-hydroxyethylsulfanyl)decylsulfanyl]ethanol

The solubility of 2-[10-(2-hydroxyethylsulfanyl)decylsulfanyl]ethanol can be characterized by several factors that influence its behavior in various solvents:

  • Polarity: This compound possesses both polar and non-polar characteristics. The hydroxyethyl and ethanol portions introduce hydrophilic nature, while the long decyl chain contributes a hydrophobic aspect.
  • Solvent Interaction: It is likely to be soluble in polar solvents such as water and alcohols due to its hydroxyl group, while exhibiting limited solubility in non-polar solvents.
  • Hydrogen Bonding: The presence of the hydroxyl (-OH) group facilitates hydrogen bonding, enhancing solubility in suitable polar environments.
  • Temperature Effects: Like many compounds, solubility can increase with temperature; thus, heating the solvent may improve the dissolution process.

In summary, the solubility of **2-[10-(2-hydroxyethylsulfanyl)decylsulfanyl]ethanol** is heavily influenced by its molecular structure, specifically its ability to form hydrogen bonds and interact with polar solvents. Understanding these solubility characteristics is vital for applications in various chemical processes and formulations.

Interesting facts

Interesting Facts about 2-[10-(2-hydroxyethylsulfanyl)decylsulfanyl]ethanol

2-[10-(2-hydroxyethylsulfanyl)decylsulfanyl]ethanol, a compound with striking structural complexity, is a part of a fascinating category of molecules known as thiols and thioethers. These compounds play a crucial role in various biological and chemical processes.

Key Characteristics

  • Biological Significance: Many sulfanyl-containing compounds are known to exhibit antimicrobial properties. This characteristic makes them a point of interest for researchers looking to develop new antiseptic agents.
  • Versatile Applications: 2-[10-(2-hydroxyethylsulfanyl)decylsulfanyl]ethanol can be utilized in surfactants and emulsifiers due to its amphiphilic nature, which allows it to interact with both hydrophilic and hydrophobic phases.
  • Environmental Impact: Sulfur compounds have been studied for their potential role in pollution treatment processes, as they can be used to remove heavy metals and other contaminants from wastewater.

Chemical Insights

The unique structure of this compound makes it particularly intriguing. With a hydroxyethyl group along with multiple sulfur atoms, the compound exemplifies the innovation in organic synthesis. As chemists build more complex molecules like this, they open doors to discovering new functionalities and reactions.

In the realm of chemical research, 2-[10-(2-hydroxyethylsulfanyl)decylsulfanyl]ethanol reminds us of the elegance and diversity of organic chemistry. It also emphasizes the role of sulfur in creating sophisticated molecular architectures that are not only fascinating but also bear significant practical applications.

Quote to Ponder

"In every molecule, there lies a narrative waiting to be discovered." This statement resonates especially well with compounds like 2-[10-(2-hydroxyethylsulfanyl)decylsulfanyl]ethanol, where every atom contributes to the potential stories of discovery in chemistry.

Synonyms
TIADENOL
Thiadenol
Fonlipol
Eulip
Fonilap
Tiaden
finlipol
tiaterol
LL 1558
Tiadenolum
1,10-Bis(hydroxyethylthio)decane
Tiadenol [INN:DCF]
1,10-Bis(2-hydroxyethylthio)decane
2,2'-(Decamethylenedithio)diethanol
Tiadenolum [INN-Latin]
Ethanol, 2,2'-(decamethylenedithio)di-
EINECS 230-165-6
NSC 66316
NSC-66316
Tiadenol (INN)
BRN 1705474
AI3-18196
UNII-22251270CX
2,2'-(1,10-Decanediylbis(thio))bisethanol
TIADENOL [INN]
TIADENOL [MI]
2,2'-(1,10-Decanediylbis(thio))bis-ethanol
Bis(hydroxy-ethyl-thio) 1-10 decane [French]
TIADENOL [MART.]
2,2'-(decamethylenedithio)-diethanol
Bis(hydroxy-ethyl-thio) 1-10 decane
Ethanol, 2,2'-(1,10-decanediylbis(thio))bis-
TIADENOL [WHO-DD]
LL-1558
22251270CX
DTXSID50219903
3-01-00-02232 (Beilstein Handbook Reference)
tiadenolo
3,14-DITHIA-1,16-HEXADECANEDIOL
Tiadenolum (INN-Latin)
TIADENOL (MART.)
1,10-BIS(.BETA.-HYDROXYETHYLTHIO)DECANE
BS 530
bis(hydroxy-2-ethylthio)-1,10-decane
2-((10-((2-hydroxyethyl)sulfanyl)decyl)sulfanyl)ethan-1-ol
2-({10-[(2-hydroxyethyl)sulfanyl]decyl}sulfanyl)ethan-1-ol
C10AX03
DTXCID60142394
bis(2-hydroxyethylthio)-1,10-decane
1,10-BIS(BETA-HYDROXYETHYLTHIO)DECANE
Ethanol, 2,2'-(1,10-decanediylbis(thio))bis-(9CI)
delipid
6964-20-1
Tiadenol [DCF:INN]
2-[10-(2-hydroxyethylsulfanyl)decylsulfanyl]ethanol
2,2'-(decane-1,10-diylbis(sulfanediyl))bis(ethan-1-ol)
NCIOpen2_002999
SCHEMBL153097
CHEMBL1697775
CHEBI:135235
WRCITXQNXAIKLR-UHFFFAOYSA-N
NSC66316
Ethanol,2'-(decamethylenedithio)di-
AKOS040754206
DB13348
NS00036906
Ethanol,2'-[1,10-decanediylbis(thio)]bis-
D07191
Q7800043