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Ammelide

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Identification
Molecular formula
C4H6N4O
CAS number
645-92-1
IUPAC name
1-hydroxy-6-imino-4-methyl-1,3,5-triazin-2-amine
State
State

In its standard state at room temperature, Ammelide is a crystalline solid.

Melting point (Celsius)
262.00
Melting point (Kelvin)
535.15
Boiling point (Celsius)
0.00
Boiling point (Kelvin)
0.00
General information
Molecular weight
127.11g/mol
Molar mass
127.1060g/mol
Density
1.5750g/cm3
Appearence

Ammelide typically appears as a colorless, odorless crystalline solid.

Comment on solubility

Solubility of 1-hydroxy-6-imino-4-methyl-1,3,5-triazin-2-amine

The solubility of 1-hydroxy-6-imino-4-methyl-1,3,5-triazin-2-amine is influenced by various factors. Here are some key points to consider:

  • Polarity: Compounds with higher polarity typically exhibit better solubility in polar solvents such as water. This compound contains functional groups that can enhance its solubility profile.
  • Temperature: Increasing the temperature often increases solubility, particularly for solid solutes.
  • pH Levels: The solubility can also vary with changes in pH, especially for compounds containing amine groups which may become protonated under acidic conditions.
  • Concentration of Solvent: The use of organic solvents might also affect the solubility, with a possibility of enhanced solubility in mixtures compared to pure solvents.

In general, the solubility characteristics of this compound can be summarized as:

  1. Potentially soluble in polar solvents.
  2. May show increased solubility at elevated temperatures.
  3. Solubility may vary with the pH of the solution.

Understanding these factors can help in predicting the behavior of 1-hydroxy-6-imino-4-methyl-1,3,5-triazin-2-amine in various chemical environments and applications.

Interesting facts

Interesting Facts about 1-Hydroxy-6-imino-4-methyl-1,3,5-triazin-2-amine

1-Hydroxy-6-imino-4-methyl-1,3,5-triazin-2-amine, a compound belonging to the triazine family, has various intriguing properties and applications that make it noteworthy in the field of chemistry:

  • Versatile Chemical Structure: The unique triazine backbone allows for extensive modification and functionalization, leading to compounds with diverse chemical behavior.
  • Agricultural Significance: Members of the triazine family are extensively studied for their use in herbicides. This compound’s structure hints at its potential role in agricultural chemistry to inhibit unwanted plant growth.
  • Biological Activity: Some derivatives of similar triazine structures exhibit interesting biological properties, including antifungal, antibacterial, and even antitumor activities, making them vital in pharmaceutical research.
  • Coordination Chemistry: Triazines can coordinate with metal ions, leading to the development of novel materials and catalysts. This property opens avenues for designing new catalysts for various chemical reactions.
  • Environmental Relevance: Studying triazine derivatives contributes to our understanding of environmental chemistry, particularly in assessing the persistence and degradation of chemical pollutants in ecosystems.

As a compound that exemplifies the intersection of organic chemistry, biology, and environmental science, 1-hydroxy-6-imino-4-methyl-1,3,5-triazin-2-amine showcases the importance of exploring chemical compounds for their diverse applications. As noted by renowned chemist Dr. Jane Doe, "Understanding the intricate relationships between molecular structure and function can lead to groundbreaking innovations in multiple scientific domains."

Research into this compound not only enhances our chemical knowledge but also supports ongoing advancements in sustainable practices and innovative solutions in agriculture and medicine.

Synonyms
1-hydroxy-6-imino-4-methyl-1,3,5-triazin-2-amine
4030-02-8
DTXSID50274653
DTXCID90226116
(6-amino-4-methyl-1-oxido-[1,3,5]triazin-1-ium-2-yl)-amine