Skip to main content

Butabarbital

ADVERTISEMENT
Identification
Molecular formula
C10H16N2O3
CAS number
125-40-6
IUPAC name
5-butyl-1,3-dimethyl-hexahydropyrimidine-2,4,6-trione
State
State

At room temperature, butabarbital is in a solid state, typically as a crystalline powder.

Melting point (Celsius)
141.50
Melting point (Kelvin)
414.65
Boiling point (Celsius)
0.00
Boiling point (Kelvin)
0.00
General information
Molecular weight
268.32g/mol
Molar mass
268.3220g/mol
Density
1.1200g/cm3
Appearence

Butabarbital typically appears as a white, crystalline powder. This compound is odorless and has a slightly bitter taste. It is stable under normal conditions of use and storage.

Comment on solubility

Solubility of 5-butyl-1,3-dimethyl-hexahydropyrimidine-2,4,6-trione

The solubility of 5-butyl-1,3-dimethyl-hexahydropyrimidine-2,4,6-trione is an important aspect to consider in various chemical applications. This compound's solubility can be influenced by several factors, which include:

  • Polarity: The presence of functional groups in the structure may lead to a higher polarity, potentially increasing its solubility in polar solvents like water.
  • Temperature: As with many compounds, increasing the temperature generally enhances solubility, allowing for a greater dissolution of the compound in solvents.
  • pH Levels: The ionic nature of a compound can vary with pH, which may significantly impact solubility in aqueous solutions.
  • Complexation: This compound may form soluble complexes with various metals, further influencing its overall solubility in different environments.

To summarize, while the exact solubility of 5-butyl-1,3-dimethyl-hexahydropyrimidine-2,4,6-trione depends on the factors mentioned above, it is clear that understanding its solubility behavior is crucial for efficient application in chemical processes and formulations. As the saying goes, "Like dissolves like," highlighting the importance of matching solvent and solute properties for achieving optimal solubility.

Interesting facts

Interesting Facts about 5-butyl-1,3-dimethyl-hexahydropyrimidine-2,4,6-trione

The compound 5-butyl-1,3-dimethyl-hexahydropyrimidine-2,4,6-trione is a fascinating molecule that belongs to the class of pyrimidines, which are essential in the world of organic chemistry. Here are some intriguing aspects of this compound:

  • Pyrimidine Core: This compound features a hexahydropyrimidine structure, which is a saturated derivative of the pyrimidine ring. Pyrimidines are known for their role in biological systems, most notably as the building blocks of RNA and DNA.
  • Diverse Applications: Compounds related to pyrimidines are often studied for their pharmaceutical benefits. They might exhibit diverse biological activities, including anti-inflammatory, antibacterial, and antitumor properties.
  • Functional Groups: The presence of multiple carbon chains and methyl groups in the structure can contribute to variations in reactivity and interaction with biological systems, making this compound a subject of interest in medicinal chemistry.
  • Synthesis Potential: The synthetic pathways to create such compounds often involve complex reactions but could lead to various derivatives that broaden their potential applications in organic synthesis and material science.
  • Chemical Behavior: The unique arrangement of substituents on the pyrimidine platform influences its chemical properties, allowing scientists to manipulate its reactivity and selectivity in various reactions.

As one delves deeper into the world of organic compounds like 5-butyl-1,3-dimethyl-hexahydropyrimidine-2,4,6-trione, it becomes clear that the diversity and adaptability of chemical structures can lead to groundbreaking discoveries in both chemistry and biology. The study of such compounds showcases the intricate connections between molecular design and functional outcomes in the realm of scientific research.

Synonyms
BARBITURIC ACID, 5-BUTYL-1,3-DIMETHYL-
7391-62-0
5-Butyl-1,3-dimethylbarbituric acid
BRN 0204473
dimethyl butyl barbiturate
4-24-00-01899 (Beilstein Handbook Reference)
SCHEMBL1263039
DTXSID00224502
NS00037573