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Ammeline thiol

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Identification
Molecular formula
C3H5N5S
CAS number
121-09-1
IUPAC name
4,6-diamino-1,3,5-triazine-2-thiol
State
State

At room temperature, Ammeline thiol exists as a solid. It is stable under normal conditions of use, handling, and storage.

Melting point (Celsius)
220.00
Melting point (Kelvin)
493.15
Boiling point (Celsius)
266.00
Boiling point (Kelvin)
539.15
General information
Molecular weight
129.15g/mol
Molar mass
129.1520g/mol
Density
1.6200g/cm3
Appearence

This compound typically appears as a white to very pale yellow crystalline solid. It is a powder and might appear slightly different based on the level of purity and the processing method used.

Comment on solubility

Solubility of 4,6-Diamino-1,3,5-triazine-2-thiol

The solubility of 4,6-diamino-1,3,5-triazine-2-thiol, a compound featuring a unique thiol functional group, can exhibit interesting characteristics. When evaluating its solubility, several factors come into play:

  • Polarity: The presence of amino groups suggests potential for polar interactions, which may enhance solubility in polar solvents like water.
  • Hydrogen Bonding: The amino groups can engage in hydrogen bonding, potentially improving solubility in various polar solvents.
  • pH Dependence: The solubility may change with pH, as the thiol group can be protonated or deprotonated, affecting overall solubility in aqueous solutions.
  • Solvent Compatibility: Testing in different solvents is crucial, as the compound may show varied solubility profiles depending on the solvent's chemical nature.

In general, compounds like 4,6-diamino-1,3,5-triazine-2-thiol that contain both polar and non-polar features tend to have moderate solubility in water and other protic solvents. The statement that "like dissolves like" applies here, indicating that the compound is likely more soluble in polar conditions. However, experimental validation is essential to establish precise solubility values and behavior.

Interesting facts

Interesting Facts about 4,6-Diamino-1,3,5-triazine-2-thiol

4,6-Diamino-1,3,5-triazine-2-thiol, often referred to as a derivative of the triazine family, has piqued the interest of chemists for various reasons. Here are some fascinating points about this compound:

  • Structural Insights: This compound features a unique triazine ring, which consists of three nitrogen atoms and three carbon atoms. Its structure positions the thiol (-SH) group at the 2-position, allowing it to exhibit novel chemical reactivity.
  • Diverse Applications: The thiol functional group in this compound makes it highly reactive. It can participate in a variety of chemical reactions, making it useful in fields such as:
    • Agricultural chemistry for developing herbicides
    • Pharmaceuticals for synthesizing active medicinal compounds
    • Materials science for creating polymers with specific properties
  • Biological Activity: Compounds like this one have shown potential biological activities, particularly in the area of antimicrobial properties. Research continues into how these interactions can be optimized for therapeutic uses.
  • Synthetic Pathways: The synthesis of 4,6-diamino-1,3,5-triazine-2-thiol can occur through various methods, and understanding these pathways is critical for chemists aiming to produce it efficiently. These methods often explore alternative solvents and reaction conditions to minimize environmental impact.
  • Research Potential: Ongoing studies are focused on exploring the compound's *redox properties*, as its thiol group may participate in oxidation-reduction reactions, making it a candidate for use in sensors and catalysts.

In summary, 4,6-diamino-1,3,5-triazine-2-thiol represents a multifaceted compound with a rich tapestry of chemical behavior, diverse applications, and significant potential for further scientific exploration. As more is learned about its properties and reactions, it is likely to continue playing a vital role in advanced chemical research.