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N-ethylmelamine

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Identification
Molecular formula
C5H11N3
CAS number
100-74-3
IUPAC name
N-ethyl-1,3,5-triazin-2-amine
State
State

At room temperature, N-ethylmelamine is in a solid state. It typically appears as a crystalline white powder.

Melting point (Celsius)
84.00
Melting point (Kelvin)
357.00
Boiling point (Celsius)
218.00
Boiling point (Kelvin)
491.00
General information
Molecular weight
126.17g/mol
Molar mass
126.1670g/mol
Density
1.1400g/cm3
Appearence

N-ethylmelamine appears as a white crystalline solid. It is typically encountered in the form of a powder that is free-flowing and has no distinct odor.

Comment on solubility

Solubility of N-ethyl-1,3,5-triazin-2-amine

N-ethyl-1,3,5-triazin-2-amine is known for its intriguing solubility profile, which can be influenced by several factors. Understanding its solubility is vital for applications in various chemical processes.

Key solubility characteristics:

  • Polarity: The presence of the triazine ring can impart polar characteristics, affecting how it interacts with solvents.
  • Solvent Compatibility: This compound is typically more soluble in polar solvents such as water and alcohols, while exhibiting reduced solubility in non-polar solvents.
  • Temperature Dependence: Solubility may increase with temperature, a common trait seen in many organic compounds.
  • pH Sensitivity: Changes in pH can alter the ionization state of the compound, affecting its solubility in aqueous solutions.

To summarize, N-ethyl-1,3,5-triazin-2-amine shows good solubility in polar solvents and is influenced by factors such as temperature and pH. Understanding these aspects is crucial for optimizing its use in both laboratory and industrial settings.

Interesting facts

Interesting Facts About N-ethyl-1,3,5-triazin-2-amine

N-ethyl-1,3,5-triazin-2-amine, often referred to simply as a triazine compound, is a fascinating substance within the realm of organic chemistry. Here are some notable facts about this compound:

  • Triazine Backbone: This compound features a unique triazine ring, which is a six-membered ring containing three nitrogen atoms. The presence of nitrogen in the ring structure contributes to its distinct chemical properties and reactivity.
  • Versatile Reagent: N-ethyl-1,3,5-triazin-2-amine serves as a versatile reagent in organic synthesis, making it valuable for the development of various chemical products.
  • Applications in Agriculture: Its derivatives may be employed in agricultural applications, especially as herbicides or pesticides, due to their ability to selectively target specific plant processes.
  • Biological Activity: Research has shown that triazine derivatives can exhibit a range of biological activities, including antimicrobial and antifungal properties, making them of interest in medicinal chemistry.
  • Environmental Impact: Understanding the environmental behavior of this compound and its derivatives is crucial, especially considering their potential persistence in ecosystems.

In summary, N-ethyl-1,3,5-triazin-2-amine exemplifies the significant role that triazines play in both industrial applications and academic research. As highlighted by one chemist, "The triazine family reveals a complex interplay of structure and function, showcasing the beauty of organic chemistry."

Synonyms
N-ethyl-1,3,5-triazin-2-amine
4122-05-8
DTXSID20274660
DTXCID60226123
6-ethylamino-s-triazine
SCHEMBL4390297
AKOS006348558