Skip to main content

Isoborneol

ADVERTISEMENT
Identification
Molecular formula
C10H18O
CAS number
124-76-5
IUPAC name
6-hydroxy-1,7,7-trimethyl-norbornan-2-one
State
State

At room temperature, isoborneol is typically found in a solid state. It may exhibit volatile characteristics, sublimating slightly at room temperature due to its camphoraceous properties.

Melting point (Celsius)
212.00
Melting point (Kelvin)
485.15
Boiling point (Celsius)
214.00
Boiling point (Kelvin)
487.15
General information
Molecular weight
154.25g/mol
Molar mass
154.2510g/mol
Density
1.0110g/cm3
Appearence

Isoborneol is a white, crystalline substance with a camphor-like odor. It often appears as flaky crystals or granules that are waxy to the touch.

Comment on solubility

Solubility of 6-hydroxy-1,7,7-trimethyl-norbornan-2-one

6-hydroxy-1,7,7-trimethyl-norbornan-2-one, with the chemical formula C10H18O, exhibits specific solubility characteristics that are influenced by its molecular structure. Here are some key points regarding its solubility:

  • Polarity: Due to the presence of a hydroxyl group (–OH), this compound can participate in hydrogen bonding, which typically increases solubility in polar solvents.
  • Solvent Compatibility: 6-hydroxy-1,7,7-trimethyl-norbornan-2-one is expected to be more soluble in alcohols and ethers compared to nonpolar solvents like hexane or benzene.
  • Temperature Effects: As with many organic compounds, solubility can increase with temperature, making it important to consider the conditions under which solubility is tested.

In summary, while 6-hydroxy-1,7,7-trimethyl-norbornan-2-one shows increased solubility in polar solvents due to its hydroxyl group, its degree of solubility in various solvents will be subject to the interplay of several factors such as solvent polarity and temperature. The solubility behavior is a crucial aspect for applications in organic synthesis and formulation chemistry.

Interesting facts

Exploring 6-Hydroxy-1,7,7-trimethyl-norbornan-2-one

6-Hydroxy-1,7,7-trimethyl-norbornan-2-one is a fascinating compound with a rich profile, often studied in organic chemistry for its unique structure and properties. This compound belongs to the class of norbornanes, which are notable for their bicyclic structure, offering a range of interesting characteristics:

  • Structural Intricacies: The presence of a hydroxyl group (-OH) and the three methyl groups (-CH3) contribute to its distinctive reactivity and potential for various transformations.
  • Natural Sources: Compounds like this one are often found in nature, particularly in essential oils and plant extracts, hinting at their significance in the biosynthesis pathways of various organisms.
  • Synthetic Applications: Due to its structural framework, 6-hydroxy-1,7,7-trimethyl-norbornan-2-one serves as a valuable intermediate in the synthesis of more complex organic molecules.
  • Therapeutic Potential: Some derivatives of norbornanes have been investigated for their biological activity, including antimicrobial and anti-inflammatory properties, showcasing the compound's promise in medicinal chemistry.

In summary, 6-hydroxy-1,7,7-trimethyl-norbornan-2-one exemplifies the intriguing world of organic compounds that straddle the line between simple molecular frameworks and complex biological utility. As expressed in the words of chemists, "The beauty of chemistry lies in its complexity and the endless possibilities it unveils." Exploring such compounds not only deepens our understanding of chemical interactions but also opens the door to new innovations in pharmaceuticals and material science.

Synonyms
6-hydroxycamphor
12001-40-0
6-Hydroxy-1,7,7-trimethylbicyclo[2.2.1]heptan-2-one
Exo-ketoborneol
6-hydroxycamphors
5-Hydroxy-4,7,7-trimethylbicyclo(2.2.1)heptan-3-one
CHEBI:64814
DTXSID50923179
UNOCSJVDJYDPTN-UHFFFAOYSA-N
Bicyclo(2.2.1)heptan-3-one, 5-hydroxy-4,7,7-trimethyl-
Q27133449
6-Hydroxy-1,7,7-trimethylbicyclo[2.2.1]heptan-2-one #