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Ammelide

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Identification
Molecular formula
C4H8N6
CAS number
645-92-1
IUPAC name
N2,N4,6-trimethyl-1,3,5-triazine-2,4-diamine
State
State
At room temperature, ammelide is in a solid state, typically being found as a colorless crystal or a white powder.
Melting point (Celsius)
178.00
Melting point (Kelvin)
451.00
Boiling point (Celsius)
417.00
Boiling point (Kelvin)
690.00
General information
Molecular weight
142.14g/mol
Molar mass
142.1160g/mol
Density
1.7300g/cm3
Appearence

Ammelide appears as a colorless crystalline solid. It is commonly found as a white powder. The compound is known for its crystalline nature which gives it a distinct appearance.

Comment on solubility

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

The solubility of N2,N4,6-trimethyl-1,3,5-triazine-2,4-diamine can be understood through a few key considerations:

  • Polar vs. Nonpolar: This compound possesses significant polar character due to the presence of amino (-NH2) groups which can interact with polar solvents.
  • Solvent Interactions: It tends to be more soluble in polar solvents like water compared to nonpolar solvents due to hydrogen bonding capabilities.
  • Temperature Effects: Solubility can vary with temperature; typically, heating the solvent can enhance the dissolution rate of many organic compounds.
  • pH Influence: The pH of the solution can affect the ionization of the amino groups, thereby impacting solubility.

In summary, it is important to note that:

  1. N2,N4,6-trimethyl-1,3,5-triazine-2,4-diamine is more soluble in polar solvents.
  2. Its solubility is influenced by temperature and pH.

This complexity illustrates the need to consider multiple factors when evaluating the solubility of chemical compounds like N2,N4,6-trimethyl-1,3,5-triazine-2,4-diamine, making solubility a fascinating aspect of chemical science.

Interesting facts

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

N2,N4,6-trimethyl-1,3,5-triazine-2,4-diamine is a fascinating compound that plays a significant role in the field of chemistry, particularly in the context of agricultural chemistry and biochemistry. Here are some interesting facts about this unique compound:

  • History: This compound belongs to the triazine family, which has historical significance as herbicides and other agrochemicals. Its derivatives have been widely researched since the mid-20th century due to their effectiveness and versatility.
  • Chemical Structure: The triazine ring structure in this compound contributes to its stability and reactivity. The presence of methyl groups enhances its lipophilicity, influencing how it interacts with biological systems.
  • Biological Activity: Research has shown that compounds similar to this triazine can exhibit antimicrobial properties. These characteristics make them potential candidates in the development of new pharmaceuticals or agricultural solutions.
  • Research Potential: Scientists are actively exploring the use of triazine derivatives in various applications, including as dyes or in the synthesis of novel materials. The intriguing properties of this compound open up pathways for innovation in chemical manufacturing.
  • Environmental Considerations: Like many agricultural chemicals, triazines have raised environmental concerns, particularly regarding their persistence in soil and potential effects on non-target species. Understanding and mitigating these impacts continues to be a pertinent area of study.

In summary, N2,N4,6-trimethyl-1,3,5-triazine-2,4-diamine serves as a prime example of how chemical compounds can be integral to both practical applications and academic exploration. Its unique attributes and research implications make it a compound worthy of further investigation.

Synonyms
1973-06-4
N~2~,N~4~,6-Trimethyl-1,3,5-triazine-2,4-diamine
NSC4415
SCHEMBL10060205
DTXSID00274567
NSC-4415
s-Triazine, 2-methyl-4,6-bis(methylamino)-
N2,N4,6-trimethyl-1,3,5-triazine-2,4-diamine