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Oleyl Oleate

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Identification
Molecular formula
C27H52O3
CAS number
3687-45-4
IUPAC name
[2-[(2R,3S,4R)-3,4-dihydroxytetrahydrofuran-2-yl]-2-hydroxy-ethyl] octadecanoate
State
State

At room temperature, oleyl oleate is in a liquid state. It is commonly used in cosmetics and skincare formulations due to its emollient properties.

Melting point (Celsius)
-20.00
Melting point (Kelvin)
253.15
Boiling point (Celsius)
353.00
Boiling point (Kelvin)
626.15
General information
Molecular weight
480.79g/mol
Molar mass
480.7940g/mol
Density
0.8610g/cm3
Appearence

Oleyl oleate is typically a colorless to pale yellow liquid at room temperature. It is viscous and oily in texture.

Comment on solubility

Solubility of [2-[(2R,3S,4R)-3,4-dihydroxytetrahydrofuran-2-yl]-2-hydroxy-ethyl] octadecanoate

The solubility characteristics of [2-[(2R,3S,4R)-3,4-dihydroxytetrahydrofuran-2-yl]-2-hydroxy-ethyl] octadecanoate can be quite intricate due to its complex molecular structure. This compound is likely to exhibit different solubility in various solvents based on the following factors:

  • Polarity: Given the presence of hydroxyl groups (-OH) in its structure, this compound is expected to be more soluble in polar solvents such as water compared to non-polar solvents.
  • Alkyl Chain Length: The long octadecanoate (fatty acid) tail contributes to hydrophobic interactions, which might limit solubility in highly polar environments.
  • Intermolecular Forces: Hydrogen bonding interactions from the hydroxyl groups may enhance solubility in appropriate polar solvents.
  • Temperature Influence: An increase in temperature may improve solubility in some solvents, often aiding in the dissolution process.

Overall, while it is anticipated that [2-[(2R,3S,4R)-3,4-dihydroxytetrahydrofuran-2-yl]-2-hydroxy-ethyl] octadecanoate demonstrates reasonable solubility in polar solvents, the exact calculations of solubility must be determined through empirical testing, considering factors that impact solute-solvent interactions.

Interesting facts

Interesting Facts about 2-[(2R,3S,4R)-3,4-dihydroxytetrahydrofuran-2-yl]-2-hydroxy-ethyl octadecanoate

This fascinating compound belongs to the category of fatty acid esters and is notable for its unique structural features that contribute to its functionality and applications. Here are some intriguing points to consider:

  • Structure and Chirality: The compound contains a tetrahydrofuran ring with multiple hydroxyl groups, adding polarity and solubility characteristics. The stereochemistry is also significant; the specific arrangement of the hydroxyl groups is crucial for biological activity.
  • Biological Relevance: Due to its ester nature, the compound may have potential applications in biochemistry, particularly in drug delivery systems or as a biocompatible material.
  • Source: The octadecanoate portion indicates that this molecule is derived from stearic acid, a common fatty acid. This suggests that the compound may impart certain nutritional or physiological benefits associated with fatty acids.
  • Sustainable Chemistry: Compounds like this one can be synthesized from renewable resources, making them environmentally friendly options for various industrial applications.
  • Applications in Food and Cosmetics: Its properties may make it useful as an emollient in cosmetics or as a potential additive in food products, enhancing texture and moisture retention.

The synthesis of such compounds requires careful attention to chirality and purity, as even slight variations can lead to significant changes in bioactivity or chemical stability. As researchers continue to explore its potential, the full scope of this compound's applications remains an exciting area of study.

Synonyms
Glycomul S
SCHEMBL285527
NS00006891