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β-springene

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Identification
Molecular formula
C15H24
CAS number
20289-37-0
IUPAC name
7,11-dimethyl-3-methylene-dodeca-1,6,10-triene
State
State

At room temperature, β-springene is an oily liquid.

Melting point (Celsius)
-76.00
Melting point (Kelvin)
197.15
Boiling point (Celsius)
246.00
Boiling point (Kelvin)
519.15
General information
Molecular weight
204.36g/mol
Molar mass
204.3570g/mol
Density
0.8752g/cm3
Appearence

β-Springene is a colorless to pale yellow oil.

Comment on solubility

Solubility of 7,11-dimethyl-3-methylene-dodeca-1,6,10-triene

7,11-dimethyl-3-methylene-dodeca-1,6,10-triene, a hydrocarbon compound, presents intriguing characteristics regarding its solubility. Being a non-polar compound, it primarily exhibits limited solubility in polar solvents, such as water. Here's a breakdown of its solubility properties:

  • Nonpolar Nature: Due to its long hydrocarbon chain and lack of functional groups, it is generally soluble in nonpolar solvents, like hexane or benzene.
  • Water Solubility: This compound is expected to have a very low solubility in water (< 0.1 g/L), reflecting the general trend that hydrocarbons do not dissolve well in polar solvents.
  • Temperature Effects: The solubility may be affected by temperature; typically, nonpolar substances tend to have increased solubility at higher temperatures in nonpolar solvents.

In summary, while 7,11-dimethyl-3-methylene-dodeca-1,6,10-triene is insoluble in water, it finds compatibility in organic solvents where its nonpolar characteristics are favored. This solubility behavior is crucial for its application in various chemical contexts.

Interesting facts

Interesting Facts about 7,11-Dimethyl-3-methylene-dodeca-1,6,10-triene

7,11-Dimethyl-3-methylene-dodeca-1,6,10-triene, often referred to in more simplified terms as a type of terpene, is a fascinating compound that draws attention due to its unique structure and properties. This compound is part of a larger class of organic compounds known for their fragrance and flavoring potential, commonly found in various plants and essential oils.

Biological Significance

This compound plays a significant role in the natural world:

  • Plant Defense: Many terpenes, including this one, function as mechanisms for defense against herbivores and pathogens.
  • Aromatherapy and Medicine: Terpenes are often utilized in aromatherapy for their potential therapeutic properties, including stress relief and anti-inflammatory effects.
  • Aromatic Profile: They contribute to the aroma and flavor of various fruits and flowers, enhancing the sensory experience.

Synthesis and Applications

The synthesis of terpenes involves intricate enzymatic reactions, mainly through the mevalonate pathway or the methylerythritol phosphate pathway. Some key aspects include:

  • The compound can be synthesized from simpler precursors, showcasing intriguing pathways of organic synthesis.
  • These compounds are sought after in the fragrance industry, being key ingredients in perfumes and cosmetic products.
  • They are also investigated for their potential in biopesticides, offering an eco-friendly alternative in agricultural applications.

In Conclusion

The study of 7,11-Dimethyl-3-methylene-dodeca-1,6,10-triene not only expands our understanding of organic chemistry but also emphasizes the profound connection between chemistry and the natural world. As scientists continue to explore this compound, it may unlock new applications and deeper insights into the myriad of functions terpenes serve.

Synonyms
7,11-dimethyl-3-methylidenedodeca-1,6,10-triene
7,11-Dimethyl-3-methylene-1,6,10-dodecatriene
DTXSID30860230
DB-044662
NS00006241
Q27119784