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Ammelide

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Identification
Molecular formula
C9H8N6
CAS number
645-92-1
IUPAC name
N2,N4-diphenyl-1,3,5-triazine-2,4,6-triamine
State
State

At room temperature, Ammelide is a solid. It remains stable under normal conditions and does not display any significant volatility at ambient temperatures.

Melting point (Celsius)
178.00
Melting point (Kelvin)
451.15
Boiling point (Celsius)
260.00
Boiling point (Kelvin)
533.15
General information
Molecular weight
229.20g/mol
Molar mass
229.2300g/mol
Density
1.5000g/cm3
Appearence

Ammelide appears as a white crystalline solid. It is typically encountered as a powder or small crystals. The compound is known for its purity and consistent white color, which is a key characteristic of its appearance.

Comment on solubility

Solubility of N2,N4-diphenyl-1,3,5-triazine-2,4,6-triamine

The solubility of N2,N4-diphenyl-1,3,5-triazine-2,4,6-triamine in various solvents can be quite intriguing due to its chemical structure and interactions. Generally, the solubility of this compound can be influenced by factors such as temperature, pH, and the type of solvent used:

  • Apolar Solvents: This compound tends to be poorly soluble in apolar solvents due to its polar amine groups which do not favor interactions with non-polar solvents.
  • Polar Aprotic Solvents: Moderate solubility may be observed in solvents like dimethyl sulfoxide (DMSO) and dimethylformamide (DMF), which can stabilize the polar nitrogen sites.
  • Aqueous Solutions: Its solubility in water is generally low; however, the presence of functional groups may allow for some degree of solvation.

In summary, the overall solubility is characterized by a preference for polar environments, with a tendency to be more soluble in polar aprotic solvents compared to apolar ones. Understanding the solubility behavior is crucial for its application in various chemical processes and formulations.

Interesting facts

Interesting Facts about N2,N4-diphenyl-1,3,5-triazine-2,4,6-triamine

N2,N4-diphenyl-1,3,5-triazine-2,4,6-triamine is an intriguing compound that has captured the interest of scientists due to its diverse applications and unique structural properties. Here are some fascinating aspects of this compound:

  • Diverse Applications: This compound finds its uses in several fields including materials science, organic electronics, and photonics. Its ability to form stable complexes with metals makes it useful in catalysis.
  • Structural Features: The presence of triazine rings in its structure contributes to its aromaticity and stability. This structural motif is essential for electronic delocalization, enhancing the compound's chemical reactivity.
  • Research Interests: Ongoing research is investigating its potential as a luminescent material. The study of light-emitting compounds is vital for advancements in display technologies and energy-efficient lighting.
  • Bioactivity: Some derivatives of triazine compounds have shown notable bioactivity, and this compound's analogs are explored for potential therapeutic applications.
  • Environmental Implications: Compounds like N2,N4-diphenyl-1,3,5-triazine-2,4,6-triamine also raise discussions regarding their environmental impact and persistence. Understanding their chemical behavior is essential for safe application and disposal.

In summary, N2,N4-diphenyl-1,3,5-triazine-2,4,6-triamine is not just another compound; it serves as a bridge between chemistry and innovative technology. With its intricate structure and multifaceted properties, it is a prime example of how chemical research continues to unlock new possibilities.

Synonyms
n,n'-diphenylmelamine
Oprea1_223529
CHEMBL205604
SCHEMBL2253957
MB-16