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Sulcatone

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Identification
Molecular formula
C9H16O
CAS number
110-93-0
IUPAC name
2,6-dimethylhept-2-en-4-one
State
State

At room temperature, Sulcatone is a liquid. It is volatile and can evaporate readily at ambient conditions.

Melting point (Celsius)
-16.00
Melting point (Kelvin)
257.15
Boiling point (Celsius)
195.30
Boiling point (Kelvin)
468.45
General information
Molecular weight
140.23g/mol
Molar mass
140.2280g/mol
Density
0.8324g/cm3
Appearence

Sulcatone is a colorless to pale yellow liquid. It has a characteristic odor that is often described as fruity, similar to mint or ginger.

Comment on solubility

Solubility of 2,6-Dimethylhept-2-en-4-one

2,6-dimethylhept-2-en-4-one, a compound with a complex structure, exhibits specific solubility behaviors that are interesting to explore. The solubility of organic compounds like this one can often be influenced by several factors, including:

  • Polarity: This compound is relatively non-polar due to its hydrocarbon structure, which generally leads to lower solubility in polar solvents.
  • Hydrophobic Interactions: Non-polar compounds tend to dissolve better in organic solvents, such as hexane or ether, rather than in water, which is a polar solvent.
  • Temperature: As with many organic compounds, solubility may increase with temperature, allowing for more significant interaction in the solvent phase.

In practical terms, this means that 2,6-dimethylhept-2-en-4-one is likely to show:

  • Good solubility in organic solvents.
  • Poor solubility in aqueous environments.

As a rule of thumb, remember the phrase, "like dissolves like": non-polar compounds will typically find better solubility in non-polar solvents. Therefore, understanding the specific solvent interactions is crucial when working with this compound in different chemical applications.

Interesting facts

Interesting Facts about 2,6-Dimethylhept-2-en-4-one

2,6-Dimethylhept-2-en-4-one is a fascinating organic compound that showcases the diversity found within ketones. Here are some intriguing aspects of this compound:

  • Structural Characteristics: This compound features a unique structure that includes a double bond, which classifies it as an unsaturated ketone. The presence of two methyl groups on the sixth and second carbon atoms adds to its complexity.
  • Synthesis: 2,6-Dimethylhept-2-en-4-one can be synthesized through various methods. One common approach involves the aldol condensation, allowing chemists to create this compound with precision. The reaction conditions play a crucial role in determining the yield and purity of the product.
  • Reactivity: As with other ketones, this compound exhibits fascinating reactivity. It can undergo nucleophilic addition reactions, making it valuable in organic synthesis for creating more complex molecules.
  • Applications: Compounds like 2,6-dimethylhept-2-en-4-one can be used in the fragrance and flavor industry due to their appealing aromatic properties, serving as important intermediates in scent production.
  • Biological Significance: The study of such compounds often leads to insights into their biological activity. Some ketones are known to exhibit antimicrobial and anti-inflammatory properties, highlighting their potential in pharmaceutical applications.

In summary, 2,6-dimethylhept-2-en-4-one is not just another ketone; it is a compound that stands at the intersection of organic chemistry and practical application. As a chemistry student or enthusiast, understanding its structure, synthesis, and significance can deepen your appreciation for the complexities and utilities of chemical compounds.

Synonyms
2,6-DIMETHYL-2-HEPTEN-4-ONE
16525-05-6
DTXSID30167872
DTXCID7090363
SCHEMBL2220485
AKOS017742065