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Nerolidol

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Identification
Molecular formula
C15H26O
CAS number
7212-44-4
IUPAC name
diethyl-[2-[2-(1-naphthyl)pent-4-enylammonio]ethyl]ammonium;2-hydroxy-2-oxo-acetate
State
State

At room temperature, nerolidol is in a liquid state. It is often present in essential oils and fragrances due to its stable liquid form under normal conditions.

Melting point (Celsius)
-6.00
Melting point (Kelvin)
267.15
Boiling point (Celsius)
122.00
Boiling point (Kelvin)
395.15
General information
Molecular weight
222.37g/mol
Molar mass
222.3360g/mol
Density
1.0280g/cm3
Appearence

Nerolidol typically appears as a pale yellow liquid. It has a pleasant woody and floral aroma, often described as slightly similar to fresh bark or green wood. This compound is found in a variety of essential oils and contributes to their fragrant nature.

Comment on solubility

Solubility of Diethyl-[2-[2-(1-naphthyl)pent-4-enylammonio]ethyl]ammonium; 2-hydroxy-2-oxo-acetate

The solubility of diethyl-[2-[2-(1-naphthyl)pent-4-enylammonio]ethyl]ammonium; 2-hydroxy-2-oxo-acetate can be quite complex due to its unique structural characteristics. Here are some key points to consider:

  • Polarity: The presence of quaternary ammonium groups suggests that the compound could have a degree of water solubility due to ionic interactions. However, the aromatic naphthalene moiety may contribute hydrophobic characteristics that could limit solubility in polar solvents.
  • Hydrogen Bonding: The presence of the -OH (hydroxyl) group in the 2-hydroxy-2-oxo-acetate component may enhance solubility in protic solvents due to the ability to participate in hydrogen bonding.
  • Solvent Interaction: This compound may exhibit different solubility in various solvents, such as:
    • High solubility in polar protic solvents (e.g., water, alcohols) due to ionic and hydrogen bonding.
    • Reduced solubility in non-polar solvents (e.g., hexane, toluene) due to hydrophobic interactions from the naphthalene group.
  • Concentration Effects: At higher concentrations, the compound may exhibit different solubility behaviors, which can lead to the formation of aggregates or micelles, affecting its overall behavior in solution.

In summary, the solubility of diethyl-[2-[2-(1-naphthyl)pent-4-enylammonio]ethyl]ammonium; 2-hydroxy-2-oxo-acetate is influenced by its complex structure, presenting an intriguing case for solvation studies.

Interesting facts

Interesting Facts about Diethyl-[2-[2-(1-naphthyl)pent-4-enylammonio]ethyl]ammonium; 2-Hydroxy-2-Oxo-Acetate

This intriguing compound is known for its fascinating structure and potential applications in various fields, including medicinal chemistry and materials science. Here are some key points that highlight its significance:

  • Unique Structure: The compound features a complex arrangement that includes a diethylammonium group and a naphthyl moiety, showcasing the intriguing interactions between organic chemistry and pharmaceuticals.
  • Pharmacological Potential: Compounds like this one, with ammonium groups and aromatic rings, are often studied for their biological activity, including their roles as potential drug candidates or bioactive molecules.
  • Research Interest: Researchers are captivated by the compound's potential as a ligand in coordination chemistry, which may lead to innovative developments in catalysis and material engineering.
  • Applications in Drug Design: The presence of a naphthyl group is particularly noteworthy, as it is known to enhance the binding affinity of molecules to biological targets, making it a valuable feature in drug development.
  • Electrophilic Character: The presence of the vinyl group (pent-4-enyl) may render the compound useful in reactions that involve electrophilic additions, making it a noteworthy component in synthetic organic chemistry.

In conclusion, the diethyl-[2-[2-(1-naphthyl)pent-4-enylammonio]ethyl]ammonium; 2-hydroxy-2-oxo-acetate compound exemplifies the intricate tapestry of chemical research, where curiosity drives exploration into the realms of both basic and applied sciences. This compound not only invites further investigation but also serves as a reminder of the beauty and complexity inherent in the study of chemistry.

Synonyms
4-Pentenylamine, N-(2-diethylaminoethyl)-2-(1-naphthyl)-, bioxalate
10337-41-4
N-(2-Diethylaminoethyl)-beta-(2-propenyl)-1-naphthaleneethylamine bioxalate
1-NAPHTHALENEETHYLAMINE, N-(2-DIETHYLAMINOETHYL)-beta-(2-PROPENYL)-, BIOXALATE