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Methyl oleate

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Identification
Molecular formula
C19H36O2
CAS number
112-62-9
IUPAC name
methyl octadec-10-enoate
State
State

Liquid at room temperature.

Melting point (Celsius)
-20.00
Melting point (Kelvin)
253.15
Boiling point (Celsius)
216.00
Boiling point (Kelvin)
489.15
General information
Molecular weight
296.50g/mol
Molar mass
296.4970g/mol
Density
0.8737g/cm3
Appearence

Methyl oleate is a clear to pale yellow liquid.

Comment on solubility

Solubility of Methyl Octadec-10-enoate

Methyl octadec-10-enoate, with the chemical formula C19H36O2, is an interesting compound in terms of its solubility characteristics. This compound belongs to the class of esters, which often exhibit unique solubility properties.

Key points regarding its solubility include:

  • Solvent Effects: Methyl octadec-10-enoate is likely to be more soluble in organic solvents such as ethanol, acetone, and chloroform compared to water.
  • Hydrophobic Nature: Being a long-chain carbon compound, it displays a predominantly hydrophobic character that leads to its low solubility in polar solvents.
  • Temperature Dependency: Solubility can change with temperature; typically, increased temperature may enhance solubility in organic solvents, but effect on aqueous solubility remains minimal.
  • Applications: Its solubility properties make it a useful component in various applications, including perfumery and food flavoring, where it can effectively dissolve in oil-based carriers.

In summary, while methyl octadec-10-enoate displays limited solubility in water due to its hydrophobic alkyl chain, it shows promising solubility in non-polar organic solvents, making it versatile for various applications.

Interesting facts

Exploring Methyl Octadec-10-enoate

Methyl octadec-10-enoate, commonly referred to as a fatty acid methyl ester, is a fascinating compound with a variety of applications and interesting characteristics. Here are some key aspects to appreciate:

  • Source and Production: This compound is typically derived from natural fats and oils, particularly from sources like vegetable oils. Its production is often achieved through the process of transesterification, where lipids react with methanol.
  • Biological Importance: Methyl octadec-10-enoate plays a significant role in the study of lipids and membrane dynamics. Its structure, featuring a long carbon chain and a double bond, makes it an excellent model for investigating the behavior of fatty acids in biological systems.
  • Applications in Industry: This compound is not just a subject of academic interest; it is also utilized in various industries. It is commonly found in the formulation of biodiesel, which serves as a renewable energy source that helps reduce greenhouse gas emissions. Moreover, its ester properties lend themselves well to the creation of surfactants and emulsifiers used in cosmetics and food production.
  • Taste and Smell: Like many fatty esters, methyl octadec-10-enoate contributes to sensory characteristics in food products. Its presence can influence flavor and aroma profiles, making it a subject of interest in food chemistry.

Chemical Behavior

One of the captivating features of methyl octadec-10-enoate is its chemical reactivity. The double bond in its fatty acid chain introduces a degree of unsaturation, making it more reactive than saturated fatty acids. This property is particularly valuable in organic synthesis, where it serves as a precursor for various chemical transformations.

Conclusion

In summary, methyl octadec-10-enoate is a prime example of how a single compound can be linked to a multitude of scientific and practical applications. From its role in ecology and health to its industrial uses, understanding this compound opens doors to various fields of research and technology.

Synonyms
METHYL 10-OCTADECENOATE
13481-95-3
SCHEMBL3046827
10-Octadecenoic acid methyl ester
DTXSID501313659