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Glycol Oleate

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Identification
Molecular formula
C4H8O2
CAS number
922-63-4
IUPAC name
2-methoxyethyl 12-acetoxyoctadec-9-enoate
State
State

At room temperature, Glycol Oleate is in a liquid state. Due to its chemical composition, it remains in a fluid form across a range of temperatures, making it suitable as an emulsifier in different conditions.

Melting point (Celsius)
-20.00
Melting point (Kelvin)
253.10
Boiling point (Celsius)
332.50
Boiling point (Kelvin)
605.60
General information
Molecular weight
396.63g/mol
Molar mass
396.6340g/mol
Density
0.9106g/cm3
Appearence

Glycol Oleate typically appears as a pale-yellow to amber colored liquid. It is known for its smooth texture, which makes it useful in cosmetic formulations. This compound can also be slightly viscous in nature.

Comment on solubility

Solubility of 2-methoxyethyl 12-acetoxyoctadec-9-enoate

The solubility of 2-methoxyethyl 12-acetoxyoctadec-9-enoate is influenced by its unique chemical structure, which includes both hydrophilic and hydrophobic components. Understanding its solubility characteristics is important for its practical applications, particularly in formulations.

Key Factors Affecting Solubility:

  • Presence of Polar Groups: The methoxy group (-OCH3) introduces some degree of polarity, enhancing solubility in polar solvents such as water.
  • Hydrophobic Alkyl Chain: The long alkyl chain derived from octadecenoate contributes to significant hydrophobic characteristics, thus making it less soluble in water but more soluble in organic solvents.
  • Temperature Influence: Increased temperature may improve solubility for many organic compounds, potentially enabling greater dispersion in various solvents.

In practical terms, 2-methoxyethyl 12-acetoxyoctadec-9-enoate is expected to be soluble in organic solvents like ethanol, methanol, and acetone but may struggle to dissolve in water due to its predominantly hydrophobic nature. This dual functionality allows it to act as an effective emulsifier in certain formulations, bridging water and oil phases.

In summary, the solubility of this compound is a balance between its polar and nonpolar components, making it versatile for specific applications in the chemical and pharmaceutical industries.

Interesting facts

Interesting Facts about 2-methoxyethyl 12-acetoxyoctadec-9-enoate

2-methoxyethyl 12-acetoxyoctadec-9-enoate is a fascinating compound that plays a significant role in various fields of chemistry and industry. Here are some intriguing insights about this compound:

  • Structural Variety: This compound belongs to the class of esters, showcasing a unique structure characterized by the presence of both an ether and an ester functional group, which contributes to its chemical reactivity and versatility.
  • Biological Applications: Due to its structure, 2-methoxyethyl 12-acetoxyoctadec-9-enoate has potential applications in the field of biomedicine, particularly in drug formulation and delivery systems.
  • Surfactant Properties: Its amphiphilic nature may allow it to function as a surfactant, resulting in valuable properties for emulsifying agents in personal care and cosmetic products.
  • Contribution to Polymer Chemistry: This compound can be utilized in the synthesis of polymers, offering unique properties that can enhance the performance of materials in fields like packaging, coatings, and adhesives.
  • Laboratory Synthesis: The synthesis of 2-methoxyethyl 12-acetoxyoctadec-9-enoate presents an interesting challenge for organic chemists, involving techniques such as esterification and the manipulation of functional groups to achieve the desired end product.

As scientists delve deeper into the characteristics and applications of 2-methoxyethyl 12-acetoxyoctadec-9-enoate, it continues to prove itself as a compound with a lot of potential. Its interesting and complex nature fuels research, offering exciting prospects for future innovations in both chemical and pharmaceutical industries.

Synonyms
Methyl cellosolve acetyl ricinoleate