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Triallyl citrate

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Identification
Molecular formula
C15H20O6
CAS number
77-90-7
IUPAC name
triallyl prop-1-ene-1,2,3-tricarboxylate
State
State

At room temperature, triallyl citrate is in a liquid state.

Melting point (Celsius)
-55.00
Melting point (Kelvin)
218.15
Boiling point (Celsius)
300.00
Boiling point (Kelvin)
573.15
General information
Molecular weight
342.33g/mol
Molar mass
342.3270g/mol
Density
1.1800g/cm3
Appearence

Triallyl citrate is a colorless to pale yellow liquid with a faint odor. It may appear slightly viscous depending on the temperature.

Comment on solubility

Solubility of Triallyl Prop-1-ene-1,2,3-tricarboxylate

Triallyl prop-1-ene-1,2,3-tricarboxylate, known for its unique structure, exhibits interesting solubility characteristics that are important for various applications. Here are some key points about its solubility:

  • Solvent Interaction: This compound shows significant solubility in organic solvents such as ethanol, acetone, and dichloromethane.
  • Water Solubility: Due to its chemical structure, particularly the presence of multiple carboxylate groups, triallyl prop-1-ene-1,2,3-tricarboxylate has very low solubility in water.
  • Temperature Effects: Solubility may increase with temperature, so it is beneficial to conduct experiments at elevated temperatures for greater dissolution, particularly in organic solvents.
  • Dependent Factors: Factors such as pH and ionic strength of the solution can influence its solubility, especially in systems where partial ionization occurs.

Understanding the solubility of triallyl prop-1-ene-1,2,3-tricarboxylate is crucial for its use in polymer chemistry and other applications. As stated, “The solubility behavior of a compound is often a determining factor in its practical use”. Therefore, careful consideration of solvent selection and operational conditions is essential for optimal usage.

Interesting facts

Interesting Facts about Triallyl Prop-1-ene-1,2,3-tricarboxylate

Triallyl prop-1-ene-1,2,3-tricarboxylate is a fascinating compound known for its unique structure and applications in various fields. Here are some intriguing aspects to consider:

  • Versatile Uses: This compound is often utilized in polymer chemistry, specifically in the synthesis of cross-linked polymers. Its three allyl groups enable it to act as a multifunctional monomer that can create robust and resilient networks.
  • Industry Relevance: Due to its ability to form strong covalent bonds, triallyl prop-1-ene-1,2,3-tricarboxylate is employed in coatings, adhesives, and sealants, making it integral to the manufacturing sector.
  • Chemical Reactivity: The presence of the carboxylate groups enhances the compound's reactivity, allowing it to participate in various reactions such as esterification and polymerization. This reactivity makes it a subject of interest for chemists looking to develop new materials.
  • Biocompatibility: Certain derivatives of this compound can be developed for biomedical applications. Its properties can be tailored for use in drug delivery systems and as scaffolding materials in tissue engineering.
  • Environmental Considerations: As a compound used in designing new materials, its sustainability and environmental impact are critical areas of research. Developing eco-friendly alternatives or methods to minimize waste is a priority in modern chemistry.

In conclusion, triallyl prop-1-ene-1,2,3-tricarboxylate stands out due to its multifunctionality and relevance in both industrial and research contexts. Its chemical properties open up a wide range of possibilities for innovative applications, making it a compound worth exploring further in the fascinating world of chemistry.

Synonyms
Triallyl aconitate
13675-27-9
1,2,3-tris(prop-2-en-1-yl) prop-1-ene-1,2,3-tricarboxylate
SCHEMBL27658345