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Myrcene

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Identification
Molecular formula
C10H16
CAS number
123-35-3
IUPAC name
2,6-dimethylocta-1,4,6-triene
State
State

Myrcene is a liquid at room temperature.

Melting point (Celsius)
-4.10
Melting point (Kelvin)
268.05
Boiling point (Celsius)
167.00
Boiling point (Kelvin)
440.15
General information
Molecular weight
136.24g/mol
Molar mass
136.2380g/mol
Density
0.7940g/cm3
Appearence

Myrcene is a clear liquid with a yellowish hue. It emits a pleasant, slightly pungent, and resinous aroma.

Comment on solubility

Solubility of 2,6-Dimethylocta-1,4,6-triene

2,6-Dimethylocta-1,4,6-triene, a hydrocarbon compound with the formula C10H16, presents unique characteristics when it comes to solubility. Being an unsaturated alkene, its solubility in various solvents can be influenced by a number of factors:

  • Polarity: The compound is a nonpolar molecule due to the presence of carbon-hydrogen bonds. This leads to a general trend where nonpolar substances are soluble in nonpolar solvents according to the principles of "like dissolves like."
  • Solvent Compatibility: 2,6-Dimethylocta-1,4,6-triene is likely to be soluble in nonpolar solvents such as:
    • Hexane
    • Petrol
    • Chloroform
  • Water Solubility: Its solubility in polar solvents, particularly water, is minimal. As a rule, "the greater the polarity difference between solute and solvent, the lower the likelihood of solubility."

The overall solubility properties of 2,6-dimethylocta-1,4,6-triene make it an interesting target for applications in organic synthesis and materials science, especially where nonpolar environments are involved.

Interesting facts

Interesting Facts about 2,6-Dimethylocta-1,4,6-triene

2,6-Dimethylocta-1,4,6-triene is a fascinating hydrocarbon belonging to the family of trienes, which are compounds that contain multiple double bonds within their structure. Here are some interesting aspects of this compound:

  • Structure and Isomerism: The structure of 2,6-dimethylocta-1,4,6-triene showcases the presence of cis and trans isomerism due to the double bonds. This property can significantly influence its chemical reactivity and physical properties.
  • Natural Occurrences: Compounds related to 2,6-dimethylocta-1,4,6-triene can be found in nature, particularly in essential oils and plant extracts, where they may contribute to the aroma and flavor profiles.
  • Applications in Chemistry: This compound and its derivatives are of interest in synthetic organic chemistry, particularly in the development of new materials and pharmaceuticals due to their unique reactivity patterns.
  • Potential Biological Activity: Preliminary studies suggest that compounds with similar backbones may exhibit interesting biological activities, making them of potential interest in drug discovery. Their structure can affect the interaction with biological targets.
  • Energy Sources: Compounds containing multiple double bonds like 2,6-dimethylocta-1,4,6-triene can also be explored for their potential as biofuels or other renewable energy sources, making them relevant to sustainable chemistry.
  • Color and Light Absorption: The conjugated double bonds within the structure may impart interesting optical properties, which can be studied for potential applications in dye chemistry or photonic materials.

The rich chemistry surrounding 2,6-dimethylocta-1,4,6-triene opens doors to various research opportunities, underscoring the significance of studying such hydrocarbon compounds in both academic and industrial settings.

Synonyms
1,4,6-Octatriene, 2,6-dimethyl-
29949-56-2
DTXSID70275102
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