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Tris(oleyl) borate

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Identification
Molecular formula
C54H101BO3
CAS number
10601-37-1
IUPAC name
tris(octadec-9-enyl) borate
State
State

It is in a liquid state at room temperature.

Melting point (Celsius)
-40.00
Melting point (Kelvin)
233.15
Boiling point (Celsius)
386.00
Boiling point (Kelvin)
659.15
General information
Molecular weight
890.47g/mol
Molar mass
890.4690g/mol
Density
0.8850g/cm3
Appearence

Tris(oleyl) borate typically appears as a clear to pale yellow liquid.

Comment on solubility

Solubility of Tris(octadec-9-enyl) borate

Tris(octadec-9-enyl) borate, a compound characterized by its unique structure, exhibits intriguing solubility properties. Understanding its solubility is essential for applications in various fields, including materials science and organic synthesis.

Here are some key points regarding the solubility of tris(octadec-9-enyl) borate:

  • Solvent Compatibility: This compound is typically soluble in non-polar organic solvents, thanks to the long hydrocarbon chains derived from octadec-9-enyl groups.
  • Hydrophobic Nature: Given its hydrophobic characteristics, tris(octadec-9-enyl) borate is generally insoluble in water. This lack of solubility in aqueous environments limits its use in certain applications.
  • Temperature Effects: Solubility can be influenced by temperature; higher temperatures may increase its solubility in non-polar solvents.

In summary, while tris(octadec-9-enyl) borate demonstrates solubility in non-polar organic solvents, its hydrophobic characteristics limit its solubility in polar solvents, particularly water. Understanding these properties is crucial for researchers looking to utilize this compound effectively.

Interesting facts

Interesting Facts about Tris(octadec-9-enyl) Borate

Tris(octadec-9-enyl) borate is a fascinating compound that showcases the interplay between organic chemistry and materials science. Here are some captivating aspects of this compound:

  • Unique Structure: This compound consists of three octadec-9-enyl groups attached to a boron atom, creating a tri-substituted borate that has interesting chemical properties.
  • Hydrophobic Nature: The long octadec-9-enyl chains contribute to the hydrophobic characteristics of the compound, making it potentially useful in applications requiring water repellency.
  • Role in Polymer Chemistry: Due to its boron component, it can act as a Lewis acid, which is valuable in various polymerization processes. This feature enables the formation of complex polymers and networks.
  • Functionalization Potential: The octadec-9-enyl chains can be easily modified, allowing scientists to tailor the properties of the compound for specific applications, such as in drug delivery or surface modification.
  • Applications in Electronics: Its unique electrical properties make tris(octadec-9-enyl) borate a candidate for use in electronic materials, potentially aiding in the development of advanced semiconductor devices.

The versatility of tris(octadec-9-enyl) borate emphasizes the significance of boron compounds in modern chemistry. As students and researchers continue to explore their properties and applications, these compounds may lead to innovative solutions in various fields.

"The beauty of chemistry lies in its ability to not only transform substances but also create new pathways for technology and science."