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Sodium Dipyrone

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Identification
Molecular formula
C13H12N3NaO3
CAS number
68-89-3
IUPAC name
sodium;5-allyl-4,6-dioxo-5-phenyl-1H-pyrimidin-2-olate
State
State

At room temperature, Sodium Dipyrone is in a solid state, usually found as a crystalline powder.

Melting point (Celsius)
169.00
Melting point (Kelvin)
442.00
Boiling point (Celsius)
760.00
Boiling point (Kelvin)
1 033.00
General information
Molecular weight
333.37g/mol
Molar mass
333.3710g/mol
Density
1.4000g/cm3
Appearence

Sodium Dipyrone typically appears as a white to slightly yellow crystalline powder. It is often found in a hydrated form.

Comment on solubility

Solubility of Sodium 5-Allyl-4,6-dioxo-5-phenyl-1H-pyrimidin-2-olate

Sodium 5-allyl-4,6-dioxo-5-phenyl-1H-pyrimidin-2-olate exhibits unique solubility characteristics influenced by its chemical structure. Understanding its solubility behavior is crucial for applications in various fields such as pharmacology and biochemistry.

Key Points about its Solubility:

  • Water Solubility: The presence of the sodium ion typically enhances solubility in aqueous solutions, making it generally soluble in water.
  • Solvent Dependency: Solubility may vary depending on the solvent used; for instance, polar solvents may induce better solubility compared to non-polar solvents.
  • pH Influence: The solubility is also pH-dependent, which can affect the ionization state of the compound, thus impacting the overall solubility.
  • Temperature Effects: Increasing temperature often promotes solubility, though the specific response can vary based on compound interactions.

In conclusion, the solubility of sodium 5-allyl-4,6-dioxo-5-phenyl-1H-pyrimidin-2-olate is a complex interplay of ionic, pH, and temperature factors creating varied potential for possible applications. As always, it is recommended to perform empirical solubility assessments when working with this compound.

Interesting facts

Interesting Facts about Sodium; 5-Allyl-4,6-Dioxo-5-Phenyl-1H-Pyrimidin-2-Olate

The compound sodium; 5-allyl-4,6-dioxo-5-phenyl-1H-pyrimidin-2-olate is a fascinating entity in the world of organic chemistry, particularly within the realm of pyrimidine derivatives. Here are some captivating aspects of this compound:

  • Structural Significance: This compound showcases a unique ring structure typical of pyrimidines, featuring a dioxo group that contributes to its chemical reactivity. Pyrimidines are essential building blocks in nucleic acids, which makes compounds like this of considerable interest in biochemistry.
  • Versatile Functional Groups: The presence of the allyl group and phenyl ring highlights the compound's chemical versatility and its potential reactivity. These functional groups can participate in various chemical reactions, making this compound a synthetic target for chemists interested in creating more complex molecules.
  • Pharmacological Potential: Pyrimidine derivatives are known to exhibit biological activities, including anti-cancer and anti-viral properties. This specific compound could serve as a lead compound for drug development in medicinal chemistry.
  • Research Relevance: Studying such compounds can lead to advancements in understanding metabolic pathways, making them vital for research in fields like medicinal chemistry and pharmacology.

In the words of a prominent chemist, "The beauty of chemistry lies not only in the synthesis of compounds but also in understanding the molecular magic they can perform!" This compound exemplifies the intricate dance of atoms and molecules, revealing the profound connections between chemistry and life itself.

The exploration of sodium; 5-allyl-4,6-dioxo-5-phenyl-1H-pyrimidin-2-olate is just one of the many pathways chemists can take towards unlocking new possibilities in science and medicine.