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Triglycidyl ether

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Identification
Molecular formula
C9H14O4
CAS number
59653-12-6
IUPAC name
1,2-bis(oxiran-2-yl)ethane-1,2-diol
State
State

At room temperature, triglycidyl ether is a liquid. Its viscous nature makes it behave more like a very thick syrup.

Melting point (Celsius)
-20.00
Melting point (Kelvin)
253.15
Boiling point (Celsius)
191.00
Boiling point (Kelvin)
464.15
General information
Molecular weight
204.23g/mol
Molar mass
204.2270g/mol
Density
1.4800g/cm3
Appearence

Triglycidyl ether is typically presented as a clear or slightly yellowish liquid. It is known for being viscous, which means it has a thick and sticky consistency that flows slowly.

Comment on solubility

Solubility of 1,2-bis(oxiran-2-yl)ethane-1,2-diol

1,2-bis(oxiran-2-yl)ethane-1,2-diol, also known as a glycidol derivative, exhibits notable solubility characteristics that are influenced by its unique structural features. Here are some key points regarding its solubility:

  • Water Solubility: The presence of hydroxyl (-OH) groups in the compound enhances its ability to dissolve in water, making it relatively soluble in polar solvents.
  • Organic Solvents: It demonstrates good solubility in a variety of organic solvents, such as ethanol and acetone, which can facilitate its use in various chemical applications.
  • Temperature Dependent: Like many other compounds, the solubility of 1,2-bis(oxiran-2-yl)ethane-1,2-diol is positively correlated with temperature; as the temperature increases, solubility typically improves.

The unique geometric and electronic properties imparted by the oxirane and diol moieties contribute to the compound's versatility in solution chemistry. Understanding its solubility behavior is crucial for applications in various chemical syntheses and formulations.

Interesting facts

Interesting Facts about 1,2-bis(oxiran-2-yl)ethane-1,2-diol

1,2-bis(oxiran-2-yl)ethane-1,2-diol, commonly known as a glycidol derivative, is an intriguing compound in the field of organic chemistry. This compound, with its unique structure featuring two epoxide groups, presents a variety of fascinating properties and potential applications:

  • Diverse Applications: Due to the presence of both epoxide and hydroxyl functional groups, this compound can undergo various chemical reactions, making it valuable in the synthesis of polymers, resins, and other chemical intermediates.
  • Reactivity: The epoxide ring is known for its electrophilic nature, which allows it to react easily with nucleophiles. This makes 1,2-bis(oxiran-2-yl)ethane-1,2-diol a versatile building block in organic synthesis.
  • Biochemical Significance: Compounds like this have relevance in the study of biological systems. They may be investigated for their reactivity with biomolecules, which can lead to insights into biochemical pathways and interactions.
  • Environmental Impact: Understanding the behavior of such compounds in environmental contexts is critical. As they can participate in reactions leading to more complex organic pollutants, addressing their reactivity is important in environmental chemistry.

In conclusion, 1,2-bis(oxiran-2-yl)ethane-1,2-diol exemplifies the intricate balance between structure and reactivity in organic compounds. As noted by noted chemist Alexander say, "The beauty of chemistry lies in the details hidden within the molecular dance of atoms." The potential for this compound in both industrial and academic realms makes it a subject worthy of exploration.

Synonyms
1,2-bis(oxiran-2-yl)ethane-1,2-diol
5,6-Diepoxydulcitol
1,2-5,6-Dianhydro-dulcitol
Dianhydrodulcitol;Dianhydrogalactitol
1,6-Diepoxydulcitol
1,6-Dianhydrodulcitol
1,6-Dianhydromannitol
1,6-Dianhydrogalactitol
1,6-Diepoxy-D-mannitol
1,6-Dianhydro-D-mannitol
1,2:5,6-Dianhydrohexitol
1,6-Di-Anhydro-D-mannitol
Galactitol,2:5,6-dianhydro-
SCHEMBL8375579
D-Mannitol,2:5,6-dianhydro-
CHEMBL1987719
DTXSID60941768
AAFJXZWCNVJTMK-UHFFFAOYSA-N
HMS5087B08
Mannitol,2:5,6-dianhydro-, D-
MFCD00866451
NSC133129
AKOS025396866
NCI60_000711
261D203