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Isophorone

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Identification
Molecular formula
C9H14O
CAS number
78-59-1
IUPAC name
3-isopropyl-5-methyl-tetrahydrofuran-2-one
State
State

Isophorone is a liquid at room temperature.

Melting point (Celsius)
-8.10
Melting point (Kelvin)
265.05
Boiling point (Celsius)
215.20
Boiling point (Kelvin)
488.35
General information
Molecular weight
138.21g/mol
Molar mass
138.2070g/mol
Density
1.0008g/cm3
Appearence

Isophorone is a colorless to yellowish liquid with a characteristic peppermint-like odor. It is often used industrially and can appear slightly oily.

Comment on solubility

Solubility of 3-isopropyl-5-methyl-tetrahydrofuran-2-one

The solubility of 3-isopropyl-5-methyl-tetrahydrofuran-2-one (often referred to by its chemical structure) can be influenced by several factors and may exhibit interesting characteristics:

  • Polarity: The presence of a tetrahydrofuran ring structure suggests that the compound has moderate polarity. This can affect its ability to dissolve in various solvents.
  • Solvent Compatibility: It is likely to be soluble in polar organic solvents such as:
    • Acetone
    • Dimethyl sulfoxide (DMSO)
    • Ethanol
  • Water Solubility: Due to its structural features, 3-isopropyl-5-methyl-tetrahydrofuran-2-one is not expected to be significantly soluble in water, as the hydrophobic isopropyl and methyl groups reduce overall solubility.
  • Temperature Dependency: Like many organic compounds, solubility may increase with temperature, thereby making warm organic solvents more effective for dissolving this compound.

In summary, while the solubility of 3-isopropyl-5-methyl-tetrahydrofuran-2-one is influenced by its moderate polarity and structural attributes, it is best dissolved in polar organic solvents rather than in water. Understanding these solubility traits is vital for the effective use and manipulation of this compound in various applications.

Interesting facts

Interesting Facts about 3-isopropyl-5-methyl-tetrahydrofuran-2-one

3-isopropyl-5-methyl-tetrahydrofuran-2-one is a fascinating compound that belongs to the family of tetrahydrofuran derivatives. Here are some intriguing aspects of this compound:

  • Unique Structure: The presence of both isopropyl and methyl groups in its structure gives this compound distinctive properties and reactivity.
  • Applications: Compounds like 3-isopropyl-5-methyl-tetrahydrofuran-2-one are often explored for their potential applications in the development of fragrances, flavors, and in various chemical syntheses.
  • Synthesis Pathways: The synthesis of this compound may involve reactions that showcase the fascinating aspects of organic chemistry, such as nucleophilic substitutions and ring-opening reactions.
  • Natural Occurrence: Interestingly, some tetrahydrofuran derivatives can be found in nature, serving functional roles in various biochemical pathways.
  • Research Interest: Its unique molecular configuration makes it a subject of interest in organic synthesis research, where scientists explore its reactivity and interactions with other substances.

In conclusion, 3-isopropyl-5-methyl-tetrahydrofuran-2-one stands as a prime example of how structural diversity in organic compounds can lead to a wide range of fascinating properties and potential applications. Understanding such compounds enhances our knowledge of organic chemistry and opens doors to innovative uses in various industries.

Synonyms
3-Isopropyl-5-methyldihydro-2(3H)-furanone
19639-01-1
BRN 0111280
2(3H)-FURANONE, DIHYDRO-3-ISOPROPYL-5-METHYL-
5-17-09-00074 (Beilstein Handbook Reference)
SCHEMBL14360218
DTXSID60941405
5-Methyl-3-(propan-2-yl)oxolan-2-one