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Barbitone sodium

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Identification
Molecular formula
C10H11N2NaO3
CAS number
144-02-5
IUPAC name
sodium;5,5-diethyl-4,6-dioxo-1H-pyrimidin-2-olate
State
State

At room temperature, Barbitone sodium is in a solid state, appearing as a crystalline powder.

Melting point (Celsius)
253.00
Melting point (Kelvin)
526.15
Boiling point (Celsius)
210.00
Boiling point (Kelvin)
483.15
General information
Molecular weight
204.19g/mol
Molar mass
204.1930g/mol
Density
1.3210g/cm3
Appearence

Barbitone sodium typically appears as a white, crystalline powder. It is commonly odorless or nearly odorless.

Comment on solubility

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

The solubility characteristics of sodium 5,5-diethyl-4,6-dioxo-1H-pyrimidin-2-olate can be quite interesting, primarily due to its ionic nature and functional groups. Generally, the solubility of a compound is influenced by several factors:

  • Polarity: This compound contains polar functional groups which can lead to a higher solubility in polar solvents.
  • Hydrogen bonding: The presence of oxygen atoms allows for potential hydrogen bonding with water molecules, enhancing solubility.
  • Ionic nature: Being a sodium salt, it is expected to have a good solubility in water, as sodium ions typically dissociate readily in aqueous solutions.

In terms of practical applications, “the solubility of sodium salts often increases when temperature rises”, making it relevant for various chemical processes. It’s also worthwhile to note that the specific pH of the solution may significantly impact its solubility, as certain ionic compounds can precipitate out of solution in less favorable pH ranges.

To summarize, sodium 5,5-diethyl-4,6-dioxo-1H-pyrimidin-2-olate is likely to be fairly soluble in polar solvents, especially water, due to its ionic and polar characteristics, making it useful in diverse chemical applications.

Interesting facts

Interesting Facts about Sodium 5,5-Diethyl-4,6-dioxo-1H-pyrimidin-2-olate

This intriguing compound, known as sodium 5,5-diethyl-4,6-dioxo-1H-pyrimidin-2-olate, is a member of the pyrimidine family, which is significant due to its widespread occurrence in biological systems. Here are some captivating insights about this compound:

  • Pyrimidine Derivatives: Pyrimidines play a critical role in the structure of nucleic acids (DNA and RNA), contributing to genetic information transfer. This compound contains characteristic dioxo groups, enhancing its chemical diversity.
  • Solubility and Reactivity: Being a sodium salt, this compound is expected to exhibit interesting solubility properties, which can influence its reactivity in biochemical pathways, making it a potential candidate for various synthetic applications.
  • Application in Pharmaceuticals: The presence of the pyrimidine ring and the dioxo functional groups can lead to potential pharmacological properties. Studies have shown that pyrimidine derivatives exhibit various biological activities, including anti-inflammatory and anti-tumor effects.
  • Research and Development: Ongoing research focuses on modifying pyrimidine derivatives to enhance their efficacy and reduce toxicity. Sodium 5,5-diethyl-4,6-dioxo-1H-pyrimidin-2-olate may be explored for novel therapeutic agents in medical chemistry.
  • Historical Context: The study of pyrimidines has a rich history, dating back to their discovery in the late 19th century, and continues to be a vibrant area of research due to their numerous derivatives and applications in various fields.

In summary, sodium 5,5-diethyl-4,6-dioxo-1H-pyrimidin-2-olate embodies the fascinating intersection of chemistry and biology, where its structural attributes can lead to innovative applications and insights into molecular behavior. As scientists continue to unravel the complexities of pyrimidine chemistry, compounds like this one hold promise for future discoveries.