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Triethylamine Triazine

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Identification
Molecular formula
C9H21N3
CAS number
1946-04-3
IUPAC name
N2,N4,6-triethyl-1,3,5-triazine-2,4-diamine
State
State

At room temperature, Triethylamine Triazine is a liquid. It is volatile and has a low boiling point, making it suitable for use in gas applications.

Melting point (Celsius)
-114.10
Melting point (Kelvin)
159.05
Boiling point (Celsius)
89.50
Boiling point (Kelvin)
362.65
General information
Molecular weight
141.24g/mol
Molar mass
141.2370g/mol
Density
0.9870g/cm3
Appearence

Triethylamine Triazine appears as a colorless liquid with a characteristic fishy odor. The compound is typically clear and can sometimes appear pale yellow due to impurities.

Comment on solubility

Solubility of N2,N4,6-triethyl-1,3,5-triazine-2,4-diamine

The solubility of N2,N4,6-triethyl-1,3,5-triazine-2,4-diamine, a complex organic compound, is influenced by several factors, often leading to interesting behavior in various solvents.

Key Points about Solubility:

  • Polarity: The presence of numerous electronegative nitrogen atoms can enhance polarity, affecting solubility in polar solvents such as water.
  • Hydrophobicity: The triethyl groups introduce hydrophobic characteristics, which may limit solubility in highly polar environments.
  • Solvent Interaction: This compound may dissolve readily in organic solvents like ethanol or acetone, where its structure can interact favorably with solvent molecules.
  • Temperature Impact: As with many chemical compounds, increasing the temperature can enhance solubility due to the increased kinetic energy, facilitating solute-solvent interactions.

In summary, while N2,N4,6-triethyl-1,3,5-triazine-2,4-diamine may exhibit moderate solubility in *polar* solvents, its **hydrophobic** nature due to triethyl groups often makes it more compatible with *nonpolar* or moderately polar organic solvents. Understanding these solubility characteristics is crucial for practical applications and formulations involving this compound.

Interesting facts

Interesting Facts about N2,N4,6-triethyl-1,3,5-triazine-2,4-diamine

N2,N4,6-triethyl-1,3,5-triazine-2,4-diamine is a fascinating compound that belongs to the class of triazines, a group celebrated for their diverse applications in various fields, including agriculture and pharmaceuticals. Here are some compelling aspects of this compound:

  • Structural Characteristics: This compound features a triazine ring—a six-membered ring structure containing three nitrogen atoms. This unique configuration plays a crucial role in the compound's reactivity and stability.
  • Biological Activity: Many triazine derivatives have been identified for their potential biological activities, including herbicidal and fungicidal properties, making them essential in agrochemistry.
  • Versatile Applications: Beyond agriculture, triazine compounds, including derivatives like N2,N4,6-triethyl-1,3,5-triazine-2,4-diamine, are often used in the synthesis of dyes, pharmaceuticals, and even as intermediates in organic synthesis. Their adaptability makes them invaluable in industrial chemistry.
  • Synthetic Pathways: The synthesis of this compound can involve various methodologies, often employing selective reactions that showcase the nuances of organic chemistry.
  • Environmental Impact: As with many chemical compounds used in agriculture, the environmental implications of triazine derivatives are of great interest. Their behavior in ecosystems and potential for bioaccumulation are important areas of study for environmental chemists.

As a chemist, one cannot help but appreciate the intricate balance of efficiency and potential risks associated with compounds like N2,N4,6-triethyl-1,3,5-triazine-2,4-diamine. Understanding its properties and applications not only aids in advancing chemical innovations but also in ensuring environmental safety.

Synonyms
2-N,4-N,6-triethyl-1,3,5-triazine-2,4-diamine
26235-13-2
DTXSID80275037
RefChem:264058
DTXCID00226485
SCHEMBL2623096