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Ammeline

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Identification
Molecular formula
C4H6N6O
CAS number
645-36-3
IUPAC name
N-(4,6-diamino-1,3,5-triazin-2-yl)formamide
State
State

At room temperature, Ammeline is a solid and typically exists as a crystalline powder. It is stable under normal conditions.

Melting point (Celsius)
319.00
Melting point (Kelvin)
592.15
Boiling point (Celsius)
498.00
Boiling point (Kelvin)
771.15
General information
Molecular weight
127.13g/mol
Molar mass
127.1080g/mol
Density
1.5731g/cm3
Appearence

Ammeline appears as a white crystalline solid. It is often encountered as a powder and is known for its stability at room temperature.

Comment on solubility

Solubility of N-(4,6-diamino-1,3,5-triazin-2-yl)formamide

N-(4,6-diamino-1,3,5-triazin-2-yl)formamide, with the chemical formula C4H6N6O, demonstrates notable solubility characteristics largely influenced by its structural components.

Key Aspects of Solubility:

  • Polar Nature: The presence of the formamide functional group contributes to its polar characteristics, enhancing solubility in polar solvents like water.
  • Hydrogen Bonding: This compound can form hydrogen bonds due to the amine and carbonyl groups, which can further increase solubility in water.
  • Solvent Compatibility: N-(4,6-diamino-1,3,5-triazin-2-yl)formamide is likely to have high solubility in organic solvents such as methanol and ethanol, which can dissolve polar substances.

As a result, the solubility of this compound is considerably high in both polar and some moderately polar solvents. This versatility can be particularly beneficial in various applications, especially in fields such as pharmaceuticals and agricultural chemistry, where formamide derivatives are often utilized for their solubility properties.

Interesting facts

Interesting Facts about N-(4,6-diamino-1,3,5-triazin-2-yl)formamide

N-(4,6-diamino-1,3,5-triazin-2-yl)formamide is a fascinating chemical compound belonging to the class of organic compounds known for their diverse applications in various fields. Here are some intriguing aspects of this compound:

  • Structural Composition: This compound features a unique triazine ring in its structure, which is key to its reactivity and stability. The presence of multiple amino groups contributes to its versatility in chemical reactions.
  • Biological Applications: Compounds in the triazine family, like N-(4,6-diamino-1,3,5-triazin-2-yl)formamide, have been researched extensively for their potential in agricultural chemistry. They are investigated for use as herbicides and fungicides due to their ability to inhibit specific biochemical pathways in plants and fungi.
  • Pharmaceutical Potential: The triazine moiety can be found in various medicinal compounds. N-(4,6-diamino-1,3,5-triazin-2-yl)formamide may serve as a scaffold for developing new pharmaceuticals, particularly in the fight against infectious diseases and cancer.
  • Research Interest: The compound has garnered interest within the scientific community for its unique properties. Researchers are exploring its applications in materials science, especially in the development of new polymers and nanomaterials.
  • Environmental Impact: Understanding compounds like this is crucial as they can have significant ecological effects. Studies evaluate their breakdown products and potential environmental persistence, particularly concerning their application as agricultural chemicals.

In summary, N-(4,6-diamino-1,3,5-triazin-2-yl)formamide stands out due to its structural features and potential applications. As research continues, this compound may prove to be invaluable in multiple scientific domains, making it a significant point of interest for both chemists and students alike.

Synonyms
N-(4,6-Diamino-1,3,5-triazin-2-yl)formamide
13236-84-5
Formamide, N-(4,6-diamino-s-triazin-2-yl)-
DTXSID20157505
Formamide, N-(4,6-diamino-1,3,5-triazin-2-yl)-
Melamine formaldehyde resin
DTXCID8079996
603-570-4
HMMM TP155
SCHEMBL19401
BPISYIZLDVUTAP-UHFFFAOYSA-N
NS00024210