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Sodium 4-(2,4,6-triaminopyrimidin-5-yl)azobenzoate

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Identification
Molecular formula
C11H11N6NaO2
CAS number
0
IUPAC name
sodium;4-(2,4,6-triaminopyrimidin-5-yl)azobenzoate
State
State

This compound is typically a solid at room temperature.

Melting point (Celsius)
300.00
Melting point (Kelvin)
573.00
Boiling point (Celsius)
0.00
Boiling point (Kelvin)
0.00
General information
Molecular weight
323.29g/mol
Molar mass
323.2850g/mol
Density
1.4000g/cm3
Appearence

This compound typically appears as a red or orange solid. It is usually crystalline and can be found as a powder or in large crystal forms, depending on its specific preparation method.

Comment on solubility

Solubility of Sodium 4-(2,4,6-triaminopyrimidin-5-yl)azobenzoate

Sodium 4-(2,4,6-triaminopyrimidin-5-yl)azobenzoate is a chemical compound that exhibits specific solubility characteristics. Generally, the solubility of a compound can be influenced by various factors, including:

  • Polarity: The presence of polar functional groups can enhance solubility in polar solvents, such as water.
  • pH: Changes in pH can affect ionization, making the compound more or less soluble.
  • Temperature: Increased temperature often increases the solubility of solids in liquids.
  • Interactions: The ability to form hydrogen bonds with the solvent can also impact solubility.

In the case of sodium 4-(2,4,6-triaminopyrimidin-5-yl)azobenzoate, its sodium salt form suggests that it is likely soluble in water due to:

  1. The ionic nature of the sodium cation, which enhances solvation in aqueous environments.
  2. The hydrophilic properties of the triaminopyrimidine group.

As with many compounds, it's essential to note that while it may exhibit solubility in certain conditions, solubility can be variable and should be tested experimentally for precise values. Overall, its characteristics lend themselves to practical applications in various fields, potentially leveraging its solubility attributes for beneficial uses.

Interesting facts

Interesting Facts about Sodium 4-(2,4,6-triaminopyrimidin-5-yl)azobenzoate

Sodium 4-(2,4,6-triaminopyrimidin-5-yl)azobenzoate is a fascinating compound that lies at the intersection of organic chemistry and biological applications. Here are some interesting insights:

  • Structural Aspects: The compound features a complex structure that incorporates both an azobenzene moiety and a triaminopyrimidine group. This dual functionality can lead to unique interactions in various environments.
  • Potential Applications: Given the structure, sodium 4-(2,4,6-triaminopyrimidin-5-yl)azobenzoate may be explored for several applications, including:
    • Biological Research: Due to its ability to interact with nucleic acids or proteins, it could serve as a tool in biochemical assays.
    • Photodynamic Therapy: This compound's azobenzene component can undergo reversible trans-cis isomerization, making it a candidate for light-activated therapies.
    • Colorimetric Sensors: The unique properties of this compound might also be harnessed in the design of sensors for detecting various analytes.
  • Environmental Considerations: The presence of nitrogen atoms gives this compound significant potential for environmental applications, such as in the development of biodegradable materials.
  • Research Opportunities: The unique properties of sodium 4-(2,4,6-triaminopyrimidin-5-yl)azobenzoate encourage further investigation into its:
    • Chemical reactivity
    • Stability under different conditions
    • Interactions with other biomolecules
  • Historical Context: Compounds like this one represent the growing field of synthetic organic chemistry, which has evolved to allow precise modifications for tailoring properties suited for specific applications.

As researchers continue to explore sodium 4-(2,4,6-triaminopyrimidin-5-yl)azobenzoate, it is evident that its intriguing blend of structure and properties may lead to significant innovations in science and technology.