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1,2-Epoxy-3-propoxypropane

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Identification
Molecular formula
C6H12O2
CAS number
16088-62-3
IUPAC name
2-(propoxymethyl)oxirane
State
State

At room temperature, 1,2-Epoxy-3-propoxypropane is a liquid.

Melting point (Celsius)
-63.00
Melting point (Kelvin)
210.15
Boiling point (Celsius)
158.00
Boiling point (Kelvin)
431.15
General information
Molecular weight
116.16g/mol
Molar mass
116.1580g/mol
Density
0.8980g/cm3
Appearence

1,2-Epoxy-3-propoxypropane is a clear, colorless liquid. It is often characterized by its viscous consistency.

Comment on solubility

Solubility of 2-(propoxymethyl)oxirane

2-(propoxymethyl)oxirane, also known as propylene glycol diglycidyl ether, presents interesting characteristics in terms of solubility.

This compound is primarily soluble in:

  • Polar solvents: Such as water and alcohols, due to the presence of polar functional groups.
  • Organic solvents: Including acetone and ether, which can dissolve organic compounds effectively.

However, 2-(propoxymethyl)oxirane exhibits limited solubility in:

  • Non-polar solvents: Such as hexane, where its polar characteristics hinder successful dissolution.

As a general observation, the solubility of a compound like 2-(propoxymethyl)oxirane can be summarized by the phrase:

"Like dissolves like."

This highlights how polar functional groups tend to interact favorably with other polar solvents, enhancing its solubility there.

Overall, the solubility of 2-(propoxymethyl)oxirane is influenced by its molecular structure and the nature of the solvent used. Understanding this characteristic is crucial for its applications in various chemical processes.

Interesting facts

Interesting Facts About 2-(Propoxymethyl)oxirane

2-(Propoxymethyl)oxirane, often referred to as a form of oxirane, is an intriguing compound that plays a significant role in various chemical processes and applications. Here are some captivating aspects to consider:

  • Structure and Reactivity: The oxirane group, characterized by its three-membered cyclic ether structure, makes 2-(propoxymethyl)oxirane highly reactive. This structural uniqueness allows it to participate in a range of chemical reactions, including nucleophilic ring-opening reactions, which is vital in organic synthesis.
  • Uses in Industry: Due to its reactive nature, this compound is employed in manufacturing a variety of products, particularly in the production of resins, adhesives, and coatings. It serves as a precursor for creating more complex chemical entities, often enhancing the performance of industrial materials.
  • Environmental Considerations: Like many organics, understanding the environmental impact of 2-(propoxymethyl)oxirane is crucial. Efforts are ongoing to evaluate its degradation pathways and potential effects on ecosystems. It highlights the importance of sustainability in chemical production.
  • Interesting Fact: The presence of the propoxymethyl group offers versatility. It allows for tailored reactivity, enabling chemists to design reactions specific to desired products, making it a valuable tool in synthetic organic chemistry.
  • Safety and Handling: When working with 2-(propoxymethyl)oxirane, appropriate safety measures are essential. As a reactive compound, it requires careful handling and storage to prevent inadvertent polymerization or reaction with moisture in the environment.

Overall, 2-(propoxymethyl)oxirane represents a fascinating intersection of chemical innovation and practical application, serving as a testament to the continual evolution of chemical substances in our daily lives and industrial practices.

Synonyms
Propyl glycidyl ether
3126-95-2
Propane, 1,2-epoxy-3-propoxy-
(Propoxy methyl)oxirane
EINECS 221-509-6
NSC 83412
BRN 0103029
5-17-03-00011 (Beilstein Handbook Reference)
cwnoevurtvlunv-uhfffaoysa-n
2-(Propoxymethyl)oxirane
Glycidyl propyl ether
Oxirane, (propoxymethyl)-
(Propoxymethyl)oxirane
n-propyl glycidyl ether
Ether, 2,3-epoxypropyl propyl
1,2-EPOXY-3-PROPOXYPROPANE
2-(Propoxymethyl)oxirane #
NCIOpen2_001013
Propane,2-epoxy-3-propoxy-
SCHEMBL143771
DTXSID601314886
NSC83412
NSC-83412
AKOS009396397
DB-068428
NS00046049