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Linalool

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Identification
Molecular formula
C10H18O
CAS number
78-70-6
IUPAC name
2-methyl-6-methylene-oct-7-en-2-ol
State
State

Linalool is in a liquid state at room temperature. It is known for its intense aroma, which contributes to its common usage in perfumes and cosmetics.

Melting point (Celsius)
-29.00
Melting point (Kelvin)
244.15
Boiling point (Celsius)
198.00
Boiling point (Kelvin)
471.15
General information
Molecular weight
154.25g/mol
Molar mass
154.2530g/mol
Density
0.8608g/cm3
Appearence

Linalool is a colorless liquid that possesses a pleasant floral smell reminiscent of lavender. It is an oily liquid that can sometimes appear slightly viscous.

Comment on solubility

Solubility of 2-methyl-6-methylene-oct-7-en-2-ol

The solubility of 2-methyl-6-methylene-oct-7-en-2-ol can be approached by considering several key factors:

  • Polar vs. Nonpolar: As an organic compound, this molecule exhibits a combination of nonpolar hydrocarbon structure and polar hydroxyl (–OH) group.
  • Solvent Interaction: It is expected to be soluble in organic solvents such as ethanol and acetone, due to its nonpolar characteristics.
  • Solubility in Water: Generally, compounds containing hydroxyl groups can exhibit some level of solubility in water, though this may be limited due to the size and complexity of the hydrocarbon chain.
  • Concentration Effects: The degree of solubility can vary with concentration; higher concentrations may lead to reduced solubility as a result of molecular interactions.

Overall, one might summarize that “The presence of both polar and nonpolar features in 2-methyl-6-methylene-oct-7-en-2-ol suggests moderate solubility in polar solvents, particularly those that can interact favorably with the hydroxyl group, while its long hydrophobic tail may hinder solubility in water.


Interesting facts

Interesting Facts about 2-methyl-6-methylene-oct-7-en-2-ol

2-methyl-6-methylene-oct-7-en-2-ol, a fascinating compound in the realm of organic chemistry, is known for its unique structural features and diverse applications. Here are some intriguing insights about this compound:

  • Structural Complexity: This compound is classified as a terpenoid, featuring multiple double bonds and a hydroxyl group, which endows it with interesting chemical reactivity. Its structure showcases the beauty of organic molecules, where the specific arrangement of atoms leads to distinct properties.
  • Potential Biological Activity: Compounds that contain alcohol and double bonds often exhibit antimicrobial and antifungal properties. Researchers are actively studying 2-methyl-6-methylene-oct-7-en-2-ol for its potential medicinal applications.
  • Flavor and Fragrance Industry: Terpenoids are crucial in the flavor and fragrance industries. This compound may also play a role in the synthesis of more complex fragrances, further enriching the olfactory experience.
  • Chemical Reactions: Due to its double bonds, this compound can participate in various chemical reactions, such as cycloaddition and oxidation, making it a valuable intermediate for synthetic organic chemistry.
  • Research Frontiers: Ongoing studies aim to explore the compound's environmental impact as well as its role in natural biosynthetic pathways, highlighting the importance of understanding even small organic molecules in greater ecological contexts.

In conclusion, the exploration of 2-methyl-6-methylene-oct-7-en-2-ol opens doors to new scientific discoveries, ranging from its structural intricacies to potential applications in various industries. The ability of such compounds to connect nature and synthetic chemistry underscores their significance in modern science.

Synonyms
Myrcenol
2-Methyl-6-methyleneoct-7-en-2-ol
2-methyl-6-methylideneoct-7-en-2-ol
7-OCTEN-2-OL, 2-METHYL-6-METHYLENE-
2-Methyl-6-methylene-7-octen-2-ol
7-hydroxy-7-methyl-3-methylene-1-octene
UNII-X4XS5MYJ20
EINECS 208-843-8
BRN 1744474
MYRCENOL 50
DTXSID5027192
CHEBI:87529
EC 208-843-8
4-01-00-02280 (Beilstein Handbook Reference)
MYRCENOL [INCI]
DTXCID407192
duncvnhorhnonw-uhfffaoysa-n
543-39-5
3-Methylene-7-methyl-1-octen-7-ol
7-methyl-3-methylene-1-octen-7-ol
7-octen-2-ol, 2-methyl-6-methylene
X4XS5MYJ20
SCHEMBL111246
7-octen-2-ol,2-methyl-6-methylene
AKOS006272431
FM138909
DB-284378
NS00007334
Q411500