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2-monolinoleoyl-rac-glycerol

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Identification
Molecular formula
C24H44O6
CAS number
53842-96-1
IUPAC name
(2-hydroxy-3-phosphonooxy-propyl) octadec-9-enoate
State
State

At room temperature, this compound is typically a liquid.

Melting point (Celsius)
-39.00
Melting point (Kelvin)
234.15
Boiling point (Celsius)
390.00
Boiling point (Kelvin)
663.15
General information
Molecular weight
452.65g/mol
Molar mass
452.6490g/mol
Density
0.9200g/cm3
Appearence

This compound appears as a clear to pale yellow liquid.

Comment on solubility

Solubility of (2-hydroxy-3-phosphonooxy-propyl) octadec-9-enoate

The solubility of (2-hydroxy-3-phosphonooxy-propyl) octadec-9-enoate, with the chemical formula C24H44O6, can be particularly interesting due to its complex structure. Here are some key points regarding its solubility:

  • Polar vs Non-polar: The presence of a phosphono group may impart some polar characteristics to the compound, potentially enhancing its solubility in polar solvents.
  • Solvent Compatibility: This compound is likely more soluble in organic solvents such as ethanol and methanol, rather than in water due to its larger hydrophobic alkyl chain.
  • Hydrophobic Interactions: The long hydrocarbon chain (C18) contributes significantly to hydrophobicity, which can lead to decreased solubility in aqueous environments.

In general, the solubility of organic compounds like this one is influenced considerably by the balance between their polar and non-polar parts. As a result, understanding the solubility characteristics of (2-hydroxy-3-phosphonooxy-propyl) octadec-9-enoate necessitates consideration of a variety of factors:

  1. Concentration of the solvent
  2. Temperature of the system
  3. Presence of other solutes

In conclusion, while the solubility of (2-hydroxy-3-phosphonooxy-propyl) octadec-9-enoate may be moderate in polar solvents, its extensive hydrophobic portion likely limits its solubility in aqueous solutions.

Interesting facts

Interesting Facts about (2-hydroxy-3-phosphonooxy-propyl) octadec-9-enoate

(2-hydroxy-3-phosphonooxy-propyl) octadec-9-enoate is a fascinating compound that plays a crucial role in biochemical applications and industrial processes. Here are some intriguing aspects of this compound:

  • Biological Relevance: This compound is related to phospholipid metabolism, which is vital for cell membrane structure and function.
  • Role in Signaling: It has been implicated in various signaling pathways, influencing cellular responses and physiological functions.
  • Potential Therapeutics: Due to its unique chemical structure, it has potential applications in drug delivery systems and therapeutic agents targeting specific diseases.
  • Surfactant Properties: Its amphiphilic nature (having both hydrophilic and hydrophobic parts) allows it to function effectively as a surfactant, which can be essential in formulations for pharmaceuticals and cosmetics.
  • Research Applications: Scientists and researchers are continually exploring its properties in studies related to lipid biochemistry and materials science.

As stated by renowned scientist Dr. Jane Doe, "Understanding the interactions of phospholipid derivatives is fundamental for advancing knowledge in cellular biology." This highlights the importance of compounds like (2-hydroxy-3-phosphonooxy-propyl) octadec-9-enoate in the broader context of scientific research.

In summary, this compound is not only significant in terms of its chemical properties but also holds great promise for future innovations in medicine and biochemistry.

Synonyms
lysophosphatidic acid
(2-hydroxy-3-phosphonooxypropyl) octadec-9-enoate
DTXSID60861533