Glyceryl linoleate | Solubility of Things

Identification

Molecular formula

C₃₉H₇₀O₅

CAS number

542-45-0

IUPAC name

(3-hydroxy-2-octadeca-9,12-dienoyloxy-propyl) octadecanoate

State

At room temperature, Glyceryl linoleate is in a liquid state. It is commonly used in skincare products and cosmetics.

Melting point (Celsius)

-45.00

Melting point (Kelvin)

228.15

Boiling point (Celsius)

350.00

Boiling point (Kelvin)

623.15

General information

Molecular weight

620.98g/mol

Molar mass

620.9780g/mol

Density

0.9136g/cm³

Appearence

Glyceryl linoleate appears as a yellowish to colorless liquid at room temperature. It is an oily liquid that may be slightly viscous.

Comment on solubility

Solubility of (3-hydroxy-2-octadeca-9,12-dienoyloxy-propyl) octadecanoate

The solubility of (3-hydroxy-2-octadeca-9,12-dienoyloxy-propyl) octadecanoate, with the chemical formula C₃₉H₇₀O₅, presents interesting characteristics due to its complex structure. This compound, primarily composed of long hydrophobic carbon chains, is expected to have varying solubility based on environmental conditions. Here are some key points:

Hydrophobic Nature: The long hydrocarbon chains contribute to a significant degree of hydrophobicity, which generally results in poor solubility in water.
Solvent Dependency: This compound may be more soluble in organic solvents such as ethanol, chloroform, or dichloromethane, where non-polar interactions can facilitate solvation.
Temperature Effects: Increased temperatures could enhance solubility in organic solvents due to improved molecular motion and interactions.
Applications: Understanding its solubility is crucial for applications in fields like biochemistry and pharmaceuticals, where solvent choice can impact the effectiveness of drug delivery systems.

In summary, (3-hydroxy-2-octadeca-9,12-dienoyloxy-propyl) octadecanoate is likely to exhibit low solubility in aqueous environments while showing promising interactions with organic solvents, making solubility a vital consideration in its practical applications.

Interesting facts

Interesting Facts about (3-hydroxy-2-octadeca-9,12-dienoyloxy-propyl) octadecanoate

(3-hydroxy-2-octadeca-9,12-dienoyloxy-propyl) octadecanoate, a fascinating complex compound, captivates chemists and biochemists alike due to its structural intricacies and potential applications. Here are some compelling aspects of this compound:

Natural Origins: This compound derives from natural fatty acids and exhibits properties related to lipid metabolism in biological systems. Its structural components make it relevant in the study of lipids.
Functional Groups: The presence of hydroxyl and ester functional groups indicates that it could participate in diverse chemical reactions, lending itself to versatility in synthetic organic chemistry.
Potential Therapeutic Roles: With increasing interest in lipids and their roles in health, this compound may possess beneficial properties in pharmaceuticals or nutraceuticals, particularly in relation to cardiovascular health.
Biochemical Studies: It can act as a model compound in studies investigating membrane dynamics and lipid interactions, aiding in the understanding of cell signaling and membrane structure.
Environmental Relevance: As a fatty acid derivative, it can shed light on ecological interactions and biocompatibility of compounds in various biological systems, making it a valuable subject in environmental chemistry.

As we delve deeper into the chemical properties and interactions of this compound, it opens up avenues for research into how similar compounds may be leveraged in addressing modern challenges in health and the environment. The legacy of lipids continues to evolve, making studies involving (3-hydroxy-2-octadeca-9,12-dienoyloxy-propyl) octadecanoate both timely and relevant.