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Polyethylene glycol diglycidyl ether

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Identification
Molecular formula
C10H18O5
CAS number
16236-53-8
IUPAC name
2-[2-[2-[2-(oxiran-2-ylmethoxy)ethoxy]ethoxy]ethoxymethyl]oxirane
State
State

At room temperature, polyethylene glycol diglycidyl ether is in a liquid state. It is commonly used as a reactive diluent and modifier in the formulation of epoxy resins due to its liquid form.

Melting point (Celsius)
-50.00
Melting point (Kelvin)
223.15
Boiling point (Celsius)
350.00
Boiling point (Kelvin)
623.15
General information
Molecular weight
204.22g/mol
Molar mass
204.2160g/mol
Density
1.1248g/cm3
Appearence

Polyethylene glycol diglycidyl ether appears as a colorless to pale yellow liquid. It is slightly viscous and may have a faint sweet or ether-like odor. The compound is often used in liquid form for industrial applications.

Comment on solubility

Solubility of 2-[2-[2-[2-(oxiran-2-ylmethoxy)ethoxy]ethoxy]ethoxymethyl]oxirane

The solubility of 2-[2-[2-[2-(oxiran-2-ylmethoxy)ethoxy]ethoxy]ethoxymethyl]oxirane is influenced by its unique chemical structure, which includes multiple ether linkages and an epoxide group. Understanding this solubility is critical for applications in various fields, including pharmaceuticals and materials science.

Factors Affecting Solubility

  • Polarity: The presence of ether functionalities generally increases solubility in polar solvents such as water.
  • Hydrogen Bonding: The ability of the compound to engage in hydrogen bonding can enhance its solubility in alcohols and other polar solvents.
  • Chain Length: The length of the ethoxy chains may influence solubility, with longer chains potentially leading to decreased solubility in non-polar solvents.

In general, it can be stated that:

  • Hydrophilic Character: Given its multiple ether groups, this compound is expected to exhibit significant hydrophilic characteristics.
  • Solvent Choice: Solubility may vary drastically depending on the choice of solvent; common solvents like ethanol and acetone may yield higher solubility.

To summarize, while 2-[2-[2-[2-(oxiran-2-ylmethoxy)ethoxy]ethoxy]ethoxymethyl]oxirane shows promise in terms of solubility in polar solvents due to its functional groups, specific solubility testing is essential to determine its behavior in various medium effectively. Understanding this compound's solubility profile will be invaluable for its applications.

Interesting facts

Interesting Facts About 2-[2-[2-[2-(oxiran-2-ylmethoxy)ethoxy]ethoxy]ethoxymethyl]oxirane

This compound, known as a glycidyl ether derivative, offers unique possibilities in the world of polymer science and material chemistry. Here are some noteworthy aspects:

  • Versatile Building Block: The oxirane ring, also called an epoxide, is highly reactive, allowing this compound to serve as an effective building block for various chemical syntheses, particularly in the development of epoxy resins.
  • Applications in Coatings: Due to its strong adhesive properties, this compound finds applications in coatings and adhesives, providing excellent durability and resistance to chemicals and environmental degradation.
  • Incorporation in Biocompatible Materials: Its structure and functional groups allow it to be modified for use in biocompatible materials, which are essential in the biomedical field for applications such as drug delivery systems and tissue engineering.
  • Polymerization Potential: The epoxide groups in this compound can undergo ring-opening reactions, which can be utilized in the synthesis of complex polymers with tailored properties. This is particularly valuable in designing materials with specific thermal and mechanical characteristics.
  • Sustainability Options: As interest in sustainable chemistry grows, exploring the synthesis of this compound from bio-based feedstocks can lead to more environmentally friendly applications, reducing reliance on traditional petrochemical sources.

Understanding compounds like 2-[2-[2-[2-(oxiran-2-ylmethoxy)ethoxy]ethoxy]ethoxymethyl]oxirane is crucial in paving the way for innovations in fields ranging from advanced materials to biomedical applications. As researchers delve deeper into the intricacies of such compounds, their potential impacts on technology and environmentally conscious practices become ever more significant.

Synonyms
Etoglucid
Ethoglucid
1954-28-5
Etoglucide
Ethoglucide
Etoglucido
Etoglucidum
Ayerst 62013
Etoglucid [INN]
ICI-32865
Etoglucide [INN-French]
Etoglucidum [INN-Latin]
Etoglucido [INN-Spanish]
ICI 32865
Etoglucid [INN:BAN]
EINECS 217-784-7
Etoglucid (INN)
NSC 80439
NSC-80439
BRN 4311213
1,2-Bis(2-(2,3-epoxypropoxy)ethoxy)ethane
ETOGLUCID [MI]
Triethylene glycol, bis(2,3-epoxypropyl) ether
Ethane, 1,2-bis(2-(2,3-epoxypropoxy)ethoxy)-
ETOGLUCID [MART.]
ETOGLUCID [WHO-DD]
1,2:15,16-Diepoxy-4,7,10,13-tetraoxahexadecane
4,7,10,13-Tetraoxahexadecane, 1,2:15,16-diepoxy-
2,2'-(2,5,8,11-Tetraoxadodecane-1,12-diyl)bisoxirane
5-17-03-00020 (Beilstein Handbook Reference)
NSC80439
2,2'-(2,5,8,11-Tetraoxa-1,12-dodecane diyl)bisoxirane
Etoglucide (INN-French)
Etoglucidum (INN-Latin)
Etoglucido (INN-Spanish)
ETOGLUCID (MART.)
1,2-Bis[2-(2,3-epoxypropoxy)ethoxy]ethane
1,2-Bis(2-(2, 3-epoxypropoxy)ethoxy)ethane
1,2-Bis[2-(2, 3-epoxypropoxy)ethoxy]ethane
Ethane, 1, 2-bis(2-(2,3-epoxypropoxy)ethoxy)-
Ethane, 1, 2-bis[2-(2,3-epoxypropoxy)ethoxy]-
2-(12-(oxiran-2-yl)-2,5,8,11-tetraoxadodecan-1-yl)oxirane
2-[12-(oxiran-2-yl)-2,5,8,11-tetraoxadodecan-1-yl]oxirane
L01AG01
1,2:15,16-Diepoxy-4,7,10, 13-tetraoxahexadecane
4,7,10,13-Tetraoxahexadecane, 1,2:15,16-diepoxy-(8CI)
217-784-7
Epodyl
Triethylene glycol diglycidyl ether
Diglycidyltriethylene glycol
2-[2-[2-[2-(oxiran-2-ylmethoxy)ethoxy]ethoxy]ethoxymethyl]oxirane
4F9KUA0T4D
CHEBI:82542
Etoglucide; ICI 32865; NSC 80439; TDE
1,12-Di(oxiran-2-yl)-2,5,8,11-tetraoxadodecane
UNII-4F9KUA0T4D
Oxirane, 2,2'-(2,5,8,11-tetraoxadodecane-1,12-diyl)bis-
SCHEMBL8442
1,3-epoxypropoxy)ethoxy]ethane
CHEMBL460287
DTXSID80862800
UMILHIMHKXVDGH-UHFFFAOYSA-N
ICI32865
AKOS015905688
DB13339
Triethylene glycol,3-epoxypropyl) ether
WLN: T3OTJ B1O2O2O2O1- BT3OTJ
NS00046606
Ethane,2-bis[2-(2,3-epoxypropoxy)ethoxy]-
1,16-Diepoxy-4,7,10,13-tetraoxahexadecane
C19537
D07256
2,5,8,11-Tetraoxa-1,12-dodecanediyl)bisoxirane
Q548286
4,10,13-Tetraoxahexadecane, 1,2:15,16-diepoxy-
2,2'-(2,5,8,11-Tetraoxa-1,12-dodecanediyl)bisoxirane
Oxirane,2'-(2,5,8,11-tetraoxadodecane-1,12-diyl)bis-
2-[2-[2-[2-(oxiran-2-yl-methoxy)-ethoxy]-ethoxy]-ethoxy-methyl]-oxirane