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2,5-Dimethylhexa-1,3,5-triene

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Identification
Molecular formula
C8H12
CAS number
1119-16-0
IUPAC name
2,5-dimethylhexa-1,3,5-triene
State
State

At room temperature, 2,5-dimethylhexa-1,3,5-triene exists as a liquid. It is characterized by its volatility and relatively low boiling point compared to heavier hydrocarbons. It remains at its liquid state under standard laboratory conditions.

Melting point (Celsius)
-87.00
Melting point (Kelvin)
186.15
Boiling point (Celsius)
106.00
Boiling point (Kelvin)
379.15
General information
Molecular weight
94.15g/mol
Molar mass
94.1540g/mol
Density
0.8046g/cm3
Appearence

2,5-Dimethylhexa-1,3,5-triene is a colorless liquid with a hydrocarbon-like odor. It is generally clear and flows easily, typical of light organic compounds. The compound lacks color, making it visually similar to many other aliphatic hydrocarbons.

Comment on solubility

Solubility of 2,5-Dimethylhexa-1,3,5-triene

2,5-Dimethylhexa-1,3,5-triene, a hydrocarbon compound, demonstrates some interesting characteristics concerning its solubility:

  • The compound is largely non-polar, which generally results in low solubility in polar solvents like water.
  • However, it is highly soluble in non-polar solvents, such as hexane and benzene, due to similar molecular interactions.
  • Because of its structure as a conjugated diene, it exhibits some stability and reactivity, particularly in organic solutions.

It is important to note that the solubility can be influenced by factors such as temperature and the presence of other solutes. As a rule of thumb, **“like dissolves like”** applies to 2,5-dimethylhexa-1,3,5-triene, predisposing it to solubility in non-polar environments while remaining insoluble in polar solvents.


This distinction in solubility is crucial for applications involving the compound in chemical reactions and synthesis, particularly in organic chemistry contexts.

Interesting facts

Interesting Facts About 2,5-Dimethylhexa-1,3,5-triene

2,5-Dimethylhexa-1,3,5-triene is a unique organic compound that captivates the attention of chemists and enthusiasts alike due to its structural intricacies and potential applications. Here are some fascinating aspects of this compound:

  • Structure and Stability: Its structure features a long carbon chain with three double bonds, contributing to its classification as a polyunsaturated hydrocarbon. The presence of multiple double bonds provides it with a degree of reactivity that is essential in organic synthesis.
  • Natural Occurrence: Compounds similar to 2,5-dimethylhexa-1,3,5-triene can be found in various natural sources, particularly in essential oils of certain plants, where they contribute to fragrance and biological activity.
  • Pioneering Research: The study of compounds like this one has led to significant advancements in the field of organic chemistry, especially in the understanding of conjugated systems and their unique electronic properties.
  • Applications: The compound is of interest in the production of polymeric materials and as a precursor in the synthesis of more complex organic compounds, making it valuable in industrial processes.
  • Isomeric Variants: Its multiple isomeric forms provide a rich ground for comparison and study, significantly influencing physical and chemical properties. This diversity highlights the importance of structural configuration in chemical behavior.

As one delves deeper into the world of 2,5-dimethylhexa-1,3,5-triene, it becomes apparent that its study is not merely academic but can have far-reaching implications in various fields, including materials science, pharmacology, and environmental chemistry. In the words of a renowned chemist, “Every compound tells a story; it’s up to us to listen and understand.”

Synonyms
2,5-dimethylhexa-1,3,5-triene
Isopropenyl Isopren
DTXSID90871105
2,5-dimethyl-hexa-1,3,5-triene