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2,4,6-triisopropyl-1,3,5-triazine

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Identification
Molecular formula
C12H21N3
CAS number
27570-52-9
IUPAC name
2,4,6-triisopropyl-1,3,5-triazine
State
State

At room temperature, 2,4,6-triisopropyl-1,3,5-triazine is a solid. It is generally stable under normal conditions, though it should be stored properly to prevent decomposition or reaction with atmospheric moisture.

Melting point (Celsius)
81.00
Melting point (Kelvin)
354.15
Boiling point (Celsius)
315.00
Boiling point (Kelvin)
588.15
General information
Molecular weight
219.35g/mol
Molar mass
219.3450g/mol
Density
0.9700g/cm3
Appearence

2,4,6-Triisopropyl-1,3,5-triazine is a colorless solid that can appear crystalline. It has no distinct odor and is often used in the study of aromatic systems due to its interesting structural properties. Its luster may vary slightly if impurities are present.

Comment on solubility

Solubility of 2,4,6-triisopropyl-1,3,5-triazine

Understanding the solubility of 2,4,6-triisopropyl-1,3,5-triazine is crucial for its application in various chemical processes. This compound, characterized by its unique molecular structure, exhibits specific solubility behaviors:

  • Solvent Interactions: 2,4,6-triisopropyl-1,3,5-triazine is generally more soluble in organic solvents compared to polar solvents like water. This behavior can be attributed to its nonpolar nature.
  • Temperature Dependency: The solubility tends to increase with rising temperatures, which is typical for many organic compounds. This can facilitate better dissolution during chemical reactions.
  • Concentration Effects: At high concentrations, crystallization may occur, limiting its solubility. Understanding this can be vital for maintaining the desired concentration in solutions.
  • Applications: Due to its solubility properties, it is often utilized in formulations where organic solvents are used, such as in herbicides and other agrochemicals.

In summary, the solubility of 2,4,6-triisopropyl-1,3,5-triazine is influenced by factors such as the type of solvent, temperature, and concentration. Recognizing these parameters is essential for optimizing its use in various chemical applications.

Interesting facts

Interesting Facts About 2,4,6-Triisopropyl-1,3,5-triazine

2,4,6-Triisopropyl-1,3,5-triazine is a fascinating compound that showcases the diversity of nitrogen-containing heterocycles. This compound belongs to the triazine family, which is known for its unique structural characteristics and versatility in various applications. Here are some intriguing facts about this compound:

  • Structural Complexity: The presence of three isopropyl substituents on the triazine ring not only enhances its steric properties but also contributes to its chemical reactivity. Such bulky groups can influence the compound’s interactions with other molecules.
  • Agrochemical Potential: Compounds related to triazines are widely recognized for their use in agricultural chemicals, especially as herbicides. The reactivity and stability of triazines make them suitable candidates for developing effective agrochemicals.
  • Synthesis Importance: The synthesis of 2,4,6-triisopropyl-1,3,5-triazine is of particular interest in the field of organic chemistry. Researchers often explore innovative synthetic pathways to create such compounds. A common method involves utilizing nucleophilic substitution reactions in the presence of appropriate catalysts.
  • Exploration in Materials Science: Due to its unique chemical properties, this triazine derivative may find applications in materials science, potentially leading to new polymers or composite materials with desirable traits like durability and resistance to degradation.
  • Research Buzz: The study of triazine compounds continues to expand within the scientific community, drawing the attention of chemists interested in exploring not only their pharmaceutical potential but also their functions as ligands in coordination chemistry.

In summary, 2,4,6-triisopropyl-1,3,5-triazine is more than just a trivial compound; it represents a rich field of study that bridges organic synthesis, agricultural science, and materials research. Its distinct structure and potential applications invite further exploration and intrigue among chemists.

Synonyms
SCHEMBL11802553
InChI=1/C12H21N3/c1-7(2)10-13-11(8(3)4)15-12(14-10)9(5)6/h7-9H,1-6H