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2-Ethyl-1,3,5-triazine

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Identification
Molecular formula
C5H9N3
CAS number
1449-83-4
IUPAC name
2-ethyl-1,3,5-triazine
State
State

At room temperature, 2-ethyl-1,3,5-triazine is in a liquid state.

Melting point (Celsius)
-34.00
Melting point (Kelvin)
239.15
Boiling point (Celsius)
177.00
Boiling point (Kelvin)
450.15
General information
Molecular weight
97.14g/mol
Molar mass
97.1290g/mol
Density
1.0435g/cm3
Appearence

2-Ethyl-1,3,5-triazine is typically a colorless to pale yellow liquid. It possesses a distinct odor that is typical of nitrogen-containing heterocycles.

Comment on solubility

Solubility of 2-ethyl-1,3,5-triazine

When discussing the solubility of 2-ethyl-1,3,5-triazine, it's important to consider several key factors: the compound's structure, its interactions with solvents, and the conditions under which solubility is measured. This organic compound can exhibit varying degrees of solubility depending on the solvent used.

Factors Influencing Solubility

  • Polarity: The presence of ethyl groups contributes to a certain level of hydrophobicity, potentially limiting solubility in polar solvents like water.
  • Solvent Type: Solubility can significantly increase in non-polar or weakly polar organic solvents due to favorable interactions.
  • Temperature: Increased temperature often enhances solubility, allowing for higher concentrations of the compound to be dissolved.

In practice, 2-ethyl-1,3,5-triazine demonstrates limited aqueous solubility, which could affect its utility in various applications, requiring careful selection of solvents for effective use. The overall solubility behavior can be summarized as:

  1. Low solubility in water.
  2. Better solubility in organic solvents like ethanol, acetone, and chloroform.
  3. Temperature-dependent solubility characteristics.

In conclusion, understanding the solubility of 2-ethyl-1,3,5-triazine plays a crucial role in its application in chemical processes and formulations.

Interesting facts

Interesting Facts About 2-Ethyl-1,3,5-Triazine

2-Ethyl-1,3,5-triazine is a fascinating compound that has garnered attention in various scientific fields. Here are some intriguing aspects of this unique molecule:

  • Structural Characteristics: This compound belongs to the triazine family, which is characterized by a six-membered aromatic ring containing three nitrogen atoms. The substituent ethyl group introduces interesting properties and reactivity.
  • Applications: 2-Ethyl-1,3,5-triazine has found applications in several areas, including:
    • Agricultural chemistry as a potential herbicide.
    • Partner in research on nitrogen-containing heterocycles.
  • Synthesis Pathways: The synthesis of triazines often involves cyclization reactions. Researchers have developed various methods to synthesize 2-ethyl-1,3,5-triazine, highlighting the compound's versatility.
  • Reactivity: The presence of nitrogen atoms in the ring opens up potential reactions that can be harnessed to create more complex molecules useful in pharmaceuticals and agrochemicals.
  • Environmental Considerations: As with many chemical compounds, understanding the ecological impact of 2-ethyl-1,3,5-triazine and its potential breakdown products is essential for its safe application and handling.

Overall, the study of 2-ethyl-1,3,5-triazine offers a glimpse into the broader world of heterocyclic compounds and their significant roles in both synthetic and applied chemistry. Scientists continue to explore its properties and potential, making it a compound worth watching in future research endeavors.

Synonyms
SCHEMBL2605832