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Ammelide

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Identification
Molecular formula
C4H7N5O
CAS number
645-92-1
IUPAC name
6-methyl-N2,N4-diphenyl-1,3,5-triazine-2,4-diamine
State
State

At room temperature, ammelide is in the solid state, appearing as a white crystalline material.

Melting point (Celsius)
270.00
Melting point (Kelvin)
543.15
Boiling point (Celsius)
715.00
Boiling point (Kelvin)
988.15
General information
Molecular weight
213.22g/mol
Molar mass
213.2200g/mol
Density
1.4900g/cm3
Appearence

A white crystalline powder. It is relatively insoluble in water but can be dissolved in dilute acid or alkaline solutions.

Comment on solubility

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

The solubility of 6-methyl-N2,N4-diphenyl-1,3,5-triazine-2,4-diamine in various solvents is a topic of significant interest in chemical science. Understanding its solubility is crucial for applications in pharmaceuticals, agriculture, and materials science.

Factors Affecting Solubility

Several factors play a key role in determining the solubility of this particular compound:

  • Polarity: The presence of polar and non-polar groups in its structure affects how well the compound dissolves in polar solvents (like water) versus non-polar solvents (such as hexane).
  • Temperature: Increased temperatures generally enhance solubility; however, the specific behavior can vary based on the nature of the solute (in this case, the triazine derivative).
  • pH Levels: As a diamine, changes in pH can significantly affect the ionization of the functional groups, impacting solubility.

Typical Solubility Behavior

In practical terms, it is noted that:

  • This compound may exhibit low solubility in polar solvents due to steric hindrance and the hydrophobic characteristics introduced by the diphenyl and methyl groups.
  • It is often more soluble in organic solvents like acetone, ethanol, or dimethyl sulfoxide (DMSO), which can better accommodate non-polar interactions.

In conclusion, while the solubility of 6-methyl-N2,N4-diphenyl-1,3,5-triazine-2,4-diamine presents challenges, understanding its unique properties aids in its effective utilization across various scientific fields. As the saying goes, "Like dissolves like," emphasizing the importance of matching solvent polarity with the solute's characteristics.

Interesting facts

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

This intriguing compound, commonly known in the field of organic chemistry, is notable for its unique structure and diverse applications. Here are some engaging facts about it:

  • Versatile Applications: Compounds like 6-methyl-N2,N4-diphenyl-1,3,5-triazine-2,4-diamine are primarily explored in the realm of pharmaceuticals. Their ability to act as intermediates in drug development makes them crucial in synthesizing various medicinal compounds.
  • Structural Significance: The presence of the triazine ring, which consists of alternating nitrogen and carbon atoms, lends the compound interesting electronic properties that can be finely tuned. This can enhance reactivity and stability in various chemical environments.
  • Biochemical Interactions: Research has indicated that derivatives of triazine compounds can possess anti-cancer properties by interacting with specific cellular pathways. This enhances their significance in medicinal chemistry, paving the way for novel therapeutic agents.
  • Photostability: Many triazine derivatives are known for their photostable characteristics. This property is essential when considering applications in agrochemicals, where compounds must withstand prolonged exposure to sunlight.

As a powerful example of how structural diversity can lead to functional variation, 6-methyl-N2,N4-diphenyl-1,3,5-triazine-2,4-diamine exemplifies the complexity and beauty found within organic chemistry. As new research unfolds, the potential uses for this compound and its derivatives intrigue both scientists and students alike.

The compound represents a blend of intriguing theoretical concepts with practical applications, showcasing the amazing possibilities that lie within the field of chemistry.

Synonyms
SCHEMBL11936604