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6-Methylhept-3-en-1-ol

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Identification
Molecular formula
C8H16O
CAS number
16613-51-7
IUPAC name
6-methylhept-3-en-1-ol
State
State

This compound is in a liquid state at room temperature, characterized by its ability to remain fluid without solidifying under normal conditions.

Melting point (Celsius)
-96.00
Melting point (Kelvin)
177.15
Boiling point (Celsius)
186.60
Boiling point (Kelvin)
459.75
General information
Molecular weight
128.21g/mol
Molar mass
128.2120g/mol
Density
0.8320g/cm3
Appearence

6-Methylhept-3-en-1-ol is a colorless to pale yellow liquid with a mild, fatty odor. It is commonly utilized in the fragrance industry for its fresh, citrusy, and green characteristics.

Comment on solubility

Solubility of 6-methylhept-3-en-1-ol

6-methylhept-3-en-1-ol, a branched-chain alcohol, presents interesting solubility characteristics. Generally, the solubility of alcohols is influenced by two major factors:

  • Hydrophilic hydroxyl group (-OH): This functional group tends to form hydrogen bonds with water molecules, enhancing solubility in polar solvents.
  • Hydrophobic carbon chain: The longer the carbon chain, the more hydrophobic the molecule becomes, which can reduce solubility in water.

As a result, the solubility of 6-methylhept-3-en-1-ol can be summarized as follows:

  • The presence of the hydroxyl group allows for some degree of solubility in water.
  • However, the relatively long hydrocarbon chain might lead to limited solubility compared to shorter-chain alcohols.
  • It is generally more soluble in organic solvents like ethanol, acetone, or chloroform.

In practical terms, this means that while 6-methylhept-3-en-1-ol can dissolve in water, it is more efficiently dissolved in organic solvents, making it a versatile compound in various chemical applications.

Interesting facts

Interesting Facts about 6-Methylhept-3-en-1-ol

6-Methylhept-3-en-1-ol is an intriguing compound well-known in the realm of organic chemistry for its unique structure and properties. Here are some fascinating points that highlight its significance:

  • Structure Insight: This compound belongs to the class of alcohols and features an unsaturated carbon-carbon double bond, which contributes to its reactivity and potential usefulness in various chemical reactions.
  • Natural Occurrence: 6-Methylhept-3-en-1-ol can be found in some natural sources, often associated with the aroma and flavor of certain fruits. This makes it of interest in the food and fragrance industries.
  • Synthesis Routes: Chemists can synthesize this compound through several methods, including hydroformylation or olefin metathesis, showcasing its versatility and importance in synthetic organic chemistry.
  • Applications: Beyond its use in fragrances and flavors, it serves as an intermediate in the synthesis of other complex organic compounds, impacting pharmaceutical development and material science.
  • Isomerism: 6-Methylhept-3-en-1-ol exhibits structural isomerism, allowing for the existence of other structural forms with varying physical and chemical properties, which can be crucial in research and application.

In summary, 6-Methylhept-3-en-1-ol stands as a notable compound in organic chemistry, not only for its structural uniqueness but also for its applications and natural occurrences. As a compound with both theoretical significance and practical utility, it continues to pique the interest of chemists and industry professionals alike.