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Triethylene glycol

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Identification
Molecular formula
C6H14O4
CAS number
112-27-6
IUPAC name
2-[2-[2-[2-[2-[2-[2-[2-(2-hydroxyethoxy)ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethanol
State
State

At room temperature, triethylene glycol is a liquid. It remains stable under normal storage conditions and is used primarily as a solvent due to its hygroscopic nature.

Melting point (Celsius)
-7.00
Melting point (Kelvin)
266.15
Boiling point (Celsius)
285.00
Boiling point (Kelvin)
558.15
General information
Molecular weight
150.17g/mol
Molar mass
150.1740g/mol
Density
1.1270g/cm3
Appearence

Triethylene glycol is a colorless, odorless, and viscous liquid. It has a slightly sweet taste and is hygroscopic, meaning it can absorb moisture from the air. It is typically clear and is miscible with water and other polar solvents.

Comment on solubility

Solubility of 2-[2-[2-[2-[2-[2-[2-(2-hydroxyethoxy)ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethanol

The solubility of 2-[2-[2-[2-[2-[2-[2-(2-hydroxyethoxy)ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethanol (C6H14O4) is quite significant due to its chemical structure, which contains multiple hydroxy and ether groups. Here are some important points regarding its solubility:

  • Polarity: The presence of hydroxyl (-OH) groups contributes to the overall polarity of the molecule, enhancing its ability to interact with water.
  • Hydrogen Bonding: The compound can form hydrogen bonds with water molecules, facilitating its solubility in polar solvents.
  • Temperature Effect: Like many organic compounds, solubility may increase with temperature, allowing for greater interactions between solute and solvent.
  • Concentration Dependency: At higher concentrations, the solubility might reach a saturation point, beyond which no more solute can dissolve.
  • Applications: This solubility profile may make the compound useful in various formulations, particularly in pharmaceuticals and cosmetic products, where good solubility in water is often desired.

In conclusion, the solubility of 2-[2-[2-[2-[2-[2-[2-(2-hydroxyethoxy)ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethanol showcases how molecular structure intricately influences its capacity to dissolve, underscoring the importance of functional groups in determining the behavior of chemical substances in different environments.

Interesting facts

Interesting Facts about 2-[2-[2-[2-[2-[2-[2-(2-hydroxyethoxy)ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethanol

This compound, known for its complex structure, belongs to a class of chemicals often referred to as polyethoxy alcohols. Here are some fascinating aspects of this intriguing molecule:

  • Multi-layered Structure: The name of the compound hints at its remarkable branching pattern, which features multiple ethylene glycol units. This contributes to its potential versatility in various applications.
  • Surfactant Properties: Due to its amphiphilic nature, 2-[2-[2-[2-[2-[2-[2-(2-hydroxyethoxy)ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethanol can function effectively as a surfactant. This means it can lower surface tension in liquids, making it beneficial in formulations for detergents and emulsifiers.
  • Biocompatibility: The presence of hydroxyl groups in its structure suggests that this compound may exhibit biocompatibility. This property is crucial for its use in biomedical applications, such as drug delivery systems.
  • Stability in Various Conditions: The polyether linkages present in this compound contribute to its thermal and chemical stability. This makes it a suitable candidate for use in harsh chemical environments.
  • Potential for Green Chemistry: As interest in sustainable materials grows, compounds like this one are being explored for their possible roles in developing eco-friendly solvents and additives.

In summary, 2-[2-[2-[2-[2-[2-[2-(2-hydroxyethoxy)ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethanol is an exemplary compound that embodies the complexity and utility of polyethoxy alcohols. Its unique properties open the door to diverse applications across both industrial and research fields. As we further explore its capabilities, the possibilities remain tantalizing!

Synonyms
NONAETHYLENE GLYCOL
3386-18-3
3,6,9,12,15,18,21,24-Octaoxahexacosane-1,26-diol
HO-PEG9-OH
2-[2-[2-[2-[2-[2-[2-[2-(2-hydroxyethoxy)ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethanol
EINECS 222-206-1
C18H38O10
BRN 1804294
CHEBI:39784
AI3-01837
MFCD00698692
DTXSID10187492
4-01-00-02409 (Beilstein Handbook Reference)
1icj
2-(2-(2-(2-(2-(2-(2-(2-(2-hydroxyethoxy)ethoxy)ethoxy)ethoxy)ethoxy)ethoxy)ethoxy)ethoxy)ethanol
PEG9
Epitope ID:159256
PEG-9
SCHEMBL269586
DTXCID20109983
BCP29446
AKOS015839828
FH72968
AS-67676
BP-22017
SY045924
DB-048504
HY-116899
CS-0066779
N0698
NS00010525
S10648
EN300-7403031
Q27120377
HO-PEG9-OH;3,6,9,12,15,18,21,24-Octaoxahexacosane-1,26-diol