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β-Ionone

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Identification
Molecular formula
C13H20O
CAS number
14901-07-6
IUPAC name
4-(2,6,6-trimethylcyclohex-2-en-1-yl)but-3-en-2-one
State
State

At room temperature, β-Ionone is a liquid.

Melting point (Celsius)
-50.00
Melting point (Kelvin)
223.15
Boiling point (Celsius)
259.00
Boiling point (Kelvin)
532.15
General information
Molecular weight
192.30g/mol
Molar mass
192.2970g/mol
Density
0.9395g/cm3
Appearence

β-Ionone appears as a pale yellow to yellow liquid. It is known for its intense odor, which is described as woody-floral and slightly fruity.

Comment on solubility

Solubility of 4-(2,6,6-trimethylcyclohex-2-en-1-yl)but-3-en-2-one

The solubility of 4-(2,6,6-trimethylcyclohex-2-en-1-yl)but-3-en-2-one is an intriguing topic, reflecting its unique molecular structure. This compound, being organic in nature, exhibits certain patterns in solubility:

  • Polar vs. Non-Polar Solubility: Due to its hydrophobic cyclohexene structure and the presence of multiple alkyl groups, it is primarily non-polar. As a result, it is expected to have limited solubility in polar solvents like water.
  • Solvent Compatibility: It is more likely to be soluble in non-polar solvents such as hexane and benzene, where it can interact via van der Waals forces.
  • Concentration Effects: Like many organic compounds, increasing the temperature can enhance solubility, allowing for increased molecular motion and interaction with solvents.

Understanding the solubility behavior of this compound is essential for its applications in various fields, particularly in organic synthesis and material sciences. As we delve deeper into the relationships between structure and solubility, keep in mind that “like dissolves like” is a guiding principle in predicting solubility outcomes.

Interesting facts

Interesting Facts about 4-(2,6,6-trimethylcyclohex-2-en-1-yl)but-3-en-2-one

This compound, often referred to in scientific literature as a sophisticated organic molecule, showcases the intricate nature of chemical structure and reactivity. Here are some compelling insights:

  • Structural Complexity: The compound features an interesting combination of a cyclohexene ring and a butenone structure, which contributes to its unique chemistry.
  • Geometric Isomerism: Given its multiple double bonds, this compound has the potential for geometric isomers. The arrangement of substituents around these double bonds can lead to significant differences in chemical behavior.
  • Potential Applications: Compounds with similar structures may find application in the synthesis of natural products, perfumes, and even pharmaceuticals, owing to their diverse biological activities.
  • Reactivity Insights: The presence of an enone functional group signifies that this compound could participate in various nucleophilic addition reactions, making it a versatile intermediate in organic synthesis.
  • Natural Occurrence: Many compounds with similar frameworks are derived from natural sources, indicating that nature often selects these complex structures for their biochemical roles.

In summary, 4-(2,6,6-trimethylcyclohex-2-en-1-yl)but-3-en-2-one opens a window into the fascinating world of organic compounds, combining intricate structure with a wealth of chemical possibilities. Its blend of structural elements not only enhances our understanding of organic chemistry but also highlights the creative potential in molecular design.

Synonyms
.alpha.-Ionone
(3Z)-4-(2,6,6-TRIMETHYLCYCLOHEX-2-EN-1-YL)BUT-3-EN-2-ONE
DTXSID7044477
UZFLPKAIBPNNCA-UHFFFAOYSA-N
(E)-(+-)-4-(2,6,6-trimethyl-2-cyclohexen-1-yl)-3-buten-2-one
NS00079289