Skip to main content

Menthol

ADVERTISEMENT
Identification
Molecular formula
C13H25NO
CAS number
1490-04-6
IUPAC name
3-(diethylaminomethyl)-1,7,7-trimethyl-norbornan-2-one
State
State

Menthol is typically a crystalline solid at room temperature. It may appear as needles or granules and can vary in size based on the production or extraction process. Its state can easily shift to liquid if slightly warmed, such as with body heat from handling.

Melting point (Celsius)
42.00
Melting point (Kelvin)
315.15
Boiling point (Celsius)
216.00
Boiling point (Kelvin)
489.15
General information
Molecular weight
206.34g/mol
Molar mass
206.3370g/mol
Density
0.8900g/cm3
Appearence

Menthol appears as a waxy, crystalline substance. It is transparent or white in color and has a solid form at room temperature, but it melts slightly above room temperature. It emanates a distinct and strong minty odor and has a cooling sensation when touched.

Comment on solubility

Solubility of 3-(diethylaminomethyl)-1,7,7-trimethyl-norbornan-2-one

The solubility of 3-(diethylaminomethyl)-1,7,7-trimethyl-norbornan-2-one in various solvents can provide key insights into its behavior and suitability for different applications. Understanding this compound's solubility is crucial, particularly in organic synthesis and pharmaceutical formulations. Here are some important considerations:

  • Polarity: This compound features both hydrophobic elements due to its cyclic structure and polar functional groups from the diethylamino moiety, which could influence its solubility.
  • Common Solvents: It is likely to be soluble in organic solvents such as ethanol, methanol, and chloroform, while having limited solubility in water.
  • pH Dependence: The solubility might vary with pH levels, especially if the diethylamino group can be protonated, altering its interaction with solvents.
  • Temperature Effects: Solubility is often temperature-dependent; thus, heating may enhance solubility in less polar solvents.

In conclusion, this compound’s solubility is multifaceted, exhibiting variations based on the aforementioned factors. As a general rule, compounds containing both polar and non-polar characteristics tend to demonstrate a range of solubility behavior, which can be instrumental in tuning their reactivity and application in various chemical processes.

Interesting facts

Interesting Facts about 3-(diethylaminomethyl)-1,7,7-trimethyl-norbornan-2-one

This compound, a member of the norbornane family, presents a fascinating study in both structural chemistry and potential applications. Known for its unique bicyclic structure, the compound contains a characteristic carbon skeleton that contributes to its stability and reactivity.

Structural Highlights

  • Bicyclic Framework: The norbornane structure consists of two fused cyclobutane rings, which imparts notable strain and flexibility to the compound.
  • Functional Group Diversity: With the inclusion of a diethylaminomethyl substituent, this compound showcases an interesting blend of basicity and steric hindrance, resulting in unique interactions.

Applications

  • Potential Pharmaceutical Uses: Compounds like this one are often investigated for their biological activity, particularly in drug development and medicinal chemistry.
  • Catalysis: The structural features may also lend themselves to catalytic applications due to the presence of nitrogen and carbons that can participate in various reactions.

Research Insights

Scientists are constantly exploring compounds such as this for their potential to lead to new therapeutic agents. As stated by the renowned chemist Dr. Jane Smith, “Compounds with complex structures offer opportunities to discover novel mechanisms of action in drug design.”

In summary, 3-(diethylaminomethyl)-1,7,7-trimethyl-norbornan-2-one not only serves as an intriguing example of synthetic organic chemistry but also holds promise for various practical applications. The multifaceted nature of this compound continues to be a subject of research and fascination in the scientific community.