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Beta Ionone

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

At room temperature, Beta Ionone is a liquid.

Melting point (Celsius)
2.00
Melting point (Kelvin)
275.15
Boiling point (Celsius)
255.00
Boiling point (Kelvin)
528.15
General information
Molecular weight
192.30g/mol
Molar mass
192.2970g/mol
Density
0.9480g/cm3
Appearence

Beta Ionone is an oily yellow liquid with an aromatic violet odor. It is a compound derived from the degradation of carotenoids.

Comment on solubility

Solubility of 1-(2,6,6-trimethylcyclohex-2-en-1-yl)hepta-1,6-dien-3-one

The solubility of 1-(2,6,6-trimethylcyclohex-2-en-1-yl)hepta-1,6-dien-3-one can be influenced by various factors, making it a compound of interest in terms of its chemical behavior. Here are some key points to consider:

  • Polarity: The molecular structure of this compound suggests it has a degree of non-polarity due to the presence of hydrocarbon chains. Consequently, it may show limited solubility in polar solvents such as water.
  • Solvent Compatibility: This compound is more likely to dissolve in apolar solvents like hexane or toluene, due to its hydrophobic characteristics. Therefore, solvent choice is critical.
  • Temperature Effects: As with many organic compounds, increasing the temperature can enhance solubility in a given solvent, leading to increased molecular motion and stronger interactions with the solvent.
  • Structural Influence: The bulky trimethyl group in the compound's structure may hinder the ability to interact effectively with solvents, further influencing solubility.

In summary, the solubility of 1-(2,6,6-trimethylcyclohex-2-en-1-yl)hepta-1,6-dien-3-one is expected to be relatively low in polar solvents and more favorable in non-polar environments. Understanding these characteristics is essential for applications and processes involving this compound.

Interesting facts

Interesting Facts about 1-(2,6,6-trimethylcyclohex-2-en-1-yl)hepta-1,6-dien-3-one

This compound is a fascinating example of a naturally occurring organic molecule that exhibits a unique structure, making it an intriguing subject for both scientists and students alike. Often referred to in the context of terpenes and essential oils, this compound is noted for its potential uses in various fields such as flavoring, fragrance, and even pharmaceuticals.

Chemical Structure and Functionality

The presence of multiple double bonds in its heptadienone structure plays a significant role in its reactivity and potential applications. Here are some key features:

  • Conjugated Systems: The extended system of double bonds can lead to interesting optical properties, making it a subject of study in photochemistry.
  • Cyclic Structure: The trimethylcyclohexene portion introduces strain and unique steric effects, which can influence how the molecule interacts with biological systems.
  • Functional Groups: The ketone group adds to its reactivity, making it a potential intermediate in organic synthesis.

Biological Significance

Compounds like this one are often found in nature as part of complex organic mixtures. They can be significant in the following ways:

  • Flavor and Fragrance: Many compounds related to this structure are key components in essential oils, contributing to their aromatic properties.
  • Plant Defense Mechanisms: Some of these molecules act as natural pesticides or herbicides, protecting plants from pests.
  • Potential Therapeutic Applications: Research suggests that certain derivatives may possess anti-inflammatory or anti-cancer properties.

A Journey Through Synthesis

From a synthetic chemistry standpoint, devising economical and efficient methods to produce these kinds of compounds can be quite rewarding. Various pathways can be explored:

  • Cross-Coupling Reactions: These reactions can provide a route to synthesize complex structures using simpler starting materials.
  • Functional Group Manipulation: Chemists often explore how the introduction or modification of double bonds can significantly alter properties and reactivity.

In summary, 1-(2,6,6-trimethylcyclohex-2-en-1-yl)hepta-1,6-dien-3-one is a remarkable compound that exemplifies the unity of natural chemistry and practical applications. Its unique structure not only provides insights into organic synthesis but also unveils a multitude of potential applications in various industries!

Synonyms
Allyl ionone
1-(2,6,6-trimethylcyclohex-2-enyl)hepta-1,6-dien-3-one
FXCYGAGBPZQRJE-UHFFFAOYSA-N
DB-353833
NS00011942