Skip to main content

Methyl linolenate

ADVERTISEMENT
Identification
Molecular formula
C19H32O2
CAS number
301-00-8
IUPAC name
methyl 7-ethyl-9-(3-ethyl-3-methyl-oxiran-2-yl)-3-methyl-nona-2,6-dienoate
State
State

In normal conditions, methyl linolenate exists as a liquid.

Melting point (Celsius)
-57.00
Melting point (Kelvin)
216.15
Boiling point (Celsius)
216.00
Boiling point (Kelvin)
489.15
General information
Molecular weight
292.46g/mol
Molar mass
292.4780g/mol
Density
0.8852g/cm3
Appearence

Methyl linolenate is a colorless to pale yellow liquid.

Comment on solubility

Solubility of Methyl 7-Ethyl-9-(3-Ethyl-3-Methyl-Oxiran-2-Yl)-3-Methyl-Nona-2,6-Dienoate

The solubility of Methyl 7-Ethyl-9-(3-Ethyl-3-Methyl-Oxiran-2-Yl)-3-Methyl-Nona-2,6-Dienoate can be quite intriguing due to its complex structure. Here are some key points regarding its solubility:

  • Solvent Polarity: This compound is likely to be more soluble in polar solvents due to the presence of functional groups such as ethers and esters.
  • Hydrophobic Regions: The larger hydrophobic alkyl chains may hinder complete solubility in highly polar solvents, suggesting a balance between hydrophilic and hydrophobic interactions.
  • Temperature Effects: As with many organic compounds, increasing temperature may enhance solubility by increasing kinetic energy and solvent interactions.
  • Applications: Understanding the solubility is crucial for applications in pharmaceuticals and agrochemicals, where formulation in suitable solvents can affect efficacy and stability.

Overall, while the exact solubility characteristics may require experimental determination, it is clear that the intricate interactions of the compound with various solvents will play a significant role in its behavior in solution.

Interesting facts

Interesting Facts about Methyl 7-Ethyl-9-(3-Ethyl-3-Methyl-Oxiran-2-Yl)-3-Methyl-Nona-2,6-Dienoate

This compound, known as methyl 7-ethyl-9-(3-ethyl-3-methyl-oxiran-2-yl)-3-methyl-nona-2,6-dienoate, is a fascinating member of the ester family. It is particularly noteworthy due to its unique structure and significant applications in various fields. Here are some interesting facts:

  • Synthetic Versatility: Methyl esters like this compound are valuable in organic synthesis and can be transformed into numerous other functional groups, making them useful intermediates in chemical reactions.
  • Natural Products: Compounds with similar structures are often found in nature, particularly in essential oils and other natural extracts. They contribute to the fragrance and flavor profiles of many plants.
  • Food Industry Applications: Esters are extensively used in the food industry as flavoring agents and aroma compounds, leveraging their pleasant scents and tastes to enhance food products.
  • Agricultural Relevance: Many esters serve as critical ingredients in pesticide formulations or plant growth regulators, underscoring the compound's significance in agriculture.
  • Research Opportunities: This compound can also be a subject of ongoing research, particularly in the fields of materials science and pharmaceuticals as new synthetic pathways are explored.

The complexity of its structure, featuring multiple substituents and functional groups, opens doors to various chemical modifications. As students of chemistry, examining such compounds provides invaluable insight into the interplay of structure and function, emphasizing the importance of esters in both nature and industry.

In the words of the renowned chemist Linus Pauling, "The best way to have a good idea is to have lots of ideas." This sentiment rings true in the study of methyl 7-ethyl-9-(3-ethyl-3-methyl-oxiran-2-yl)-3-methyl-nona-2,6-dienoate, showcasing the limitless possibilities for discovery and innovation.

Synonyms
SCHEMBL7709823
DTXSID30945990
methyl 7-ethyl-9-(3-ethyl-3-methyloxiran-2-yl)-3-methylnona-2,6-dienoate
methyl 10,11-epoxy-7-ethyl-3,11-dimethyltrideca-2,6-dienoate