Skip to main content

1,2:3,4-diepoxybutane

ADVERTISEMENT
Identification
Molecular formula
C6H10O2
CAS number
1464-53-5
IUPAC name
2-[3-(oxiran-2-yl)propyl]oxirane
State
State

At room temperature, 1,2:3,4-diepoxybutane is a liquid. It remains in liquid form under standard laboratory conditions.

Melting point (Celsius)
-39.00
Melting point (Kelvin)
234.15
Boiling point (Celsius)
156.00
Boiling point (Kelvin)
429.15
General information
Molecular weight
86.09g/mol
Molar mass
86.0890g/mol
Density
0.8839g/cm3
Appearence

1,2:3,4-Diepoxybutane is a colorless liquid with a faint ether-like odor. It is often used in chemical synthesis and is known for being an epoxy compound, characterized by having two epoxide groups.

Comment on solubility

Solubility of 2-[3-(oxiran-2-yl)propyl]oxirane

The solubility of 2-[3-(oxiran-2-yl)propyl]oxirane, often classified as an epoxide compound, presents intriguing characteristics influenced by its unique structural properties. Here are some critical points regarding its solubility:

  • Polarity: The presence of epoxy groups generally contributes to a polar nature, enhancing its ability to dissolve in polar solvents.
  • Solvent Compatibility: It is likely to be soluble in organic solvents such as ethanol, acetone, and dimethyl sulfoxide (DMSO), while its solubility in water is typically limited.
  • Industrial Applications: Due to its low water solubility, the compound finds use in specific applications where aqueous environments are not predominant, such as in coatings and adhesives.
  • Structure-Activity Relations: The solubility might also vary significantly based on the particular substitutions on the epoxide structure, highlighting the importance of structural modifications.

In summary, while 2-[3-(oxiran-2-yl)propyl]oxirane exhibits selective solubility primarily in organic solvents, its chemical nature and applications are fundamentally shaped by these solubility traits.

Interesting facts

Interesting Facts about 2-[3-(oxiran-2-yl)propyl]oxirane

2-[3-(oxiran-2-yl)propyl]oxirane, commonly known as a type of glycidyl ether, exhibits a fascinating structure that includes an epoxide functional group. This compound stands out for several reasons:

  • Versatile Reactivity: The epoxide group present in 2-[3-(oxiran-2-yl)propyl]oxirane is known for its excellent reactivity. It can undergo ring-opening reactions, making it useful in various organic synthesis applications.
  • Applications in Polymers: This compound is a building block for the production of epoxy resins, which are widely used in coatings, adhesives, and composites due to their durability and chemical resistance.
  • Biological Activity: Compounds like 2-[3-(oxiran-2-yl)propyl]oxirane have shown potential biological activity, raising interest in pharmacological research. Studies explore how similar epoxides may interact with biomolecules.
  • Sustainability Consideration: As the industry moves towards greener chemistry, research into epoxide-based compounds may lead to more sustainable processes for synthesizing polymers and other materials.

The unique characteristics of 2-[3-(oxiran-2-yl)propyl]oxirane make it an intriguing compound for further study. As scientists continue to explore its applications, this compound could pave the way for innovations that enhance both material properties and environmental sustainability.

Synonyms
1,2,6,7-DIEPOXYHEPTANE
4247-19-2
2-[3-(oxiran-2-yl)propyl]oxirane
1,2:6,7-Diepoxyheptane
1,3-DI(OXIRAN-2-YL)PROPANE
HEPTANE, 1,2:6,7-DIEPOXY-
Oxirane, 2,2'-(1,3-propanediyl)bis-
8EYR8YME5M
BRN 0104311
UNII-8EYR8YME5M
4-19-00-00125 (Beilstein Handbook Reference)
SCHEMBL441939
DTXSID50962508
AKOS006277668
2,2'-(TRIMETHYLENE)BISOXIRANE
2,2'-(Propane-1,3-diyl)bis(oxirane)
J36.955A
2,2'-(1,3-PROPANEDIYL)BIS(OXIRANE)
Q27270270