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2-butyl-3-methyloxirane

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Identification
Molecular formula
C8H16O
CAS number
13465-66-2
IUPAC name
2-butyl-3-methyl-oxirane
State
State

At room temperature, 2-butyl-3-methyloxirane is in a liquid state.

Melting point (Celsius)
-80.00
Melting point (Kelvin)
193.15
Boiling point (Celsius)
144.90
Boiling point (Kelvin)
418.05
General information
Molecular weight
128.21g/mol
Molar mass
128.2120g/mol
Density
0.8546g/cm3
Appearence

2-Butyl-3-methyloxirane appears as a clear, colorless liquid.

Comment on solubility

Solubility of 2-butyl-3-methyl-oxirane

2-butyl-3-methyl-oxirane, commonly known as an epoxide, exhibits unique solubility characteristics that are worth noting:

  • Polar Nature: The epoxide ring structure imparts a certain level of polarity to the molecule, affecting its interactions with solvents.
  • Solvent Compatibility: This compound is generally soluble in organic solvents such as ethanol, acetone, and other similar organic materials, enabling its use in various industrial applications.
  • Water Solubility: Although 2-butyl-3-methyl-oxirane is not highly soluble in water due to its hydrophobic alkyl groups, some minor solubility can occur, particularly with increased temperature.
  • Temperature Effects: As is common with many organic compounds, increasing the temperature can enhance its solubility in most solvents, facilitating its incorporation into different formulations.

In summary, while 2-butyl-3-methyl-oxirane demonstrates limited water solubility, its compatibility with various organic solvents makes it versatile in chemical processes. Remember that "like dissolves like"; thus, selecting the appropriate solvent is key to maximizing the solubility of this compound.

Interesting facts

Exploring 2-butyl-3-methyl-oxirane

2-butyl-3-methyl-oxirane, often referred to simply as a cyclic ether or epoxide, is a fascinating compound with several unique properties and applications. This compound, part of the oxirane family, is notable for its three-membered ring structure, which introduces strain and reactivity into its molecular makeup.

Key Characteristics

  • Reactivity: The strained three-membered ring of oxiranes makes them highly reactive due to the angle strain. This property allows them to participate in a variety of chemical reactions, including nucleophilic ring-opening reactions.
  • Applications: 2-butyl-3-methyl-oxirane finds applications in the synthesis of various materials, including resins and polymers, due to its ability to form cross-linked structures.
  • Synthesis: It is often synthesized through the epoxidation of alkenes, showcasing the versatility of oxidation reactions in organic chemistry.
  • Biological Interaction: This compound can interact with biological molecules, making it a subject of interest in medicinal chemistry for its potential role in drug development.

Furthermore, the presence of both butyl and methyl groups in its structure contributes to its unique profile in chemoselectivity and reaction pathways. In synthetic organic chemistry, understanding the properties of such epoxides is critical because:

  • They can serve as intermediates in the synthesis of more complex molecules.
  • Their reactivity can be influenced by substituents, which opens up avenues for designing specific chemical reactions.

As one student of chemistry remarked, "The study of epoxides reveals how small changes in structure can lead to large differences in reactivity and function." Exploring 2-butyl-3-methyl-oxirane not only enhances our understanding of organic compounds but also broadens our perspective on the intricate dance of atoms that defines chemical reactivity.

Synonyms
2-BUTYL-3-METHYLOXIRANE
14925-96-3
DTXSID80933600
DTXCID901362258
(2R,3S)-2alpha-Methyl-3alpha-butyloxirane
cis-2,3-Epoxyheptane
SCHEMBL51211
SCHEMBL7689986
SCHEMBL7693277