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2-butyl-3-ethyl-oxirane

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Identification
Molecular formula
C8H16O
CAS number
13490-02-9
IUPAC name
2-butyl-3-ethyl-oxirane
State
State

At room temperature, 2-butyl-3-ethyl-oxirane is in the liquid state.

Melting point (Celsius)
-80.00
Melting point (Kelvin)
193.15
Boiling point (Celsius)
163.00
Boiling point (Kelvin)
436.15
General information
Molecular weight
128.21g/mol
Molar mass
128.2120g/mol
Density
0.8631g/cm3
Appearence

Appearance: 2-butyl-3-ethyl-oxirane is a colorless liquid with a characteristic ether-like odor.

Comment on solubility

Solubility of 2-butyl-3-ethyl-oxirane

The solubility of 2-butyl-3-ethyl-oxirane, a cyclic ether also known as an epoxide, can be quite interesting to explore. This compound tends to exhibit distinct solubility behaviors based on several factors, including temperature and the presence of other solvents. Here are some key points regarding its solubility:

  • Non-polar Nature: Due to its hydrophobic carbon chain structure, 2-butyl-3-ethyl-oxirane is relatively insoluble in water.
  • Solvophilic Properties: It is, however, soluble in organic solvents such as alcohols, ethers, and hydrocarbons, which can enhance its dissolving capability.
  • Temperature Effects: An increase in temperature often leads to increased solubility in organic solvents, allowing for more effective mixing and reactions.
  • Functional Groups: The presence of functional groups or polar attachments can influence solubility, making it more favorable in some mixtures.

In conclusion, while 2-butyl-3-ethyl-oxirane is not soluble in water, it thrives in various organic environments. As with many chemical compounds, understanding its solubility mechanics helps in predicting its behavior in different chemical processes.

Interesting facts

Interesting Facts about 2-butyl-3-ethyl-oxirane

2-butyl-3-ethyl-oxirane, a member of the epoxide family, is a fascinating compound that plays a crucial role in organic chemistry and industrial applications. Here are some intriguing facts about this compound:

  • Structure and Reactivity: As a three-membered cyclic ether, 2-butyl-3-ethyl-oxirane exhibits unique strain characteristics that render it highly reactive. This reactivity allows it to participate in various nucleophilic reactions, making it an important intermediate in the synthesis of other organic compounds.
  • Applications in Industry: The derivatives of this compound are utilized in the production of plastics, resins, and coatings. They offer enhanced durability and resistance to chemicals, which is essential for creating high-performance materials.
  • Biochemical Significance: Epoxides like 2-butyl-3-ethyl-oxirane can influence biological systems. Their reactivity with nucleophiles can lead to the formation of bioactive compounds, which may impact human health and environmental chemistry.
  • Synthetic Pathways: Chemists have developed various methods for synthesizing 2-butyl-3-ethyl-oxirane, often involving the reaction of alkenes with peracids. These pathways illustrate the compound's significance in synthetic organic chemistry.
  • Environmental Concerns: The reactivity of epoxides raises environmental considerations, as some can be toxic or hazardous. The handling, disposal, and regulatory measures surrounding their use are essential topics in both research and industrial practice.

In conclusion, 2-butyl-3-ethyl-oxirane is not just another chemical compound; it represents the intersection of chemistry, industry, and environmental science. As scientists continue to explore its properties and applications, this compound remains a vital subject of study in the field of organic chemistry.

Synonyms
3,4-Epoxyoctane
2-Butyl-3-ethyloxirane
90482-62-5
DTXSID30920368
RefChem:1062678
DTXCID301349280
291-865-5
EINECS 291-865-5
4,5-Epoxy-n-octane
EINECS 248-448-8
OCTANE, 4,5-EPOXY-
SCHEMBL51695
SCHEMBL1027449
SCHEMBL10800832
SCHEMBL28184199
QKHUXWLXTLMABH-UHFFFAOYSA-N
NS00064737