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1,3-Dibutylimidazolidin-2-one

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Identification
Molecular formula
C11H22N2O
CAS number
33328-17-7
IUPAC name
1,3-dibutylimidazolidin-2-one
State
State

At room temperature, 1,3-dibutylimidazolidin-2-one is in a liquid state.

Melting point (Celsius)
-60.00
Melting point (Kelvin)
213.15
Boiling point (Celsius)
253.00
Boiling point (Kelvin)
526.15
General information
Molecular weight
198.31g/mol
Molar mass
198.3230g/mol
Density
1.0085g/cm3
Appearence

1,3-Dibutylimidazolidin-2-one is typically found as a colorless liquid. It may also be slightly yellowish depending on impurities or exposure to air and light.

Comment on solubility

Solubility of 1,3-dibutylimidazolidin-2-one

1,3-dibutylimidazolidin-2-one, a fascinating compound in the realm of organic chemistry, presents intriguing solubility characteristics. Understanding its solubility is essential for applications involving synthesis, formulation, and reactivity. Here's what we know:

  • Polarity: The presence of the imidazolidinone structure contributes to this compound's polar nature, which can enhance solubility in polar solvents.
  • Solvent Compatibility: 1,3-dibutylimidazolidin-2-one is generally soluble in various organic solvents such as:
    • Water
    • Alcohols (e.g., ethanol, methanol)
    • Dimethyl sulfoxide (DMSO)
    • Acetone
  • Hydrophobic Chains: However, the butyl substituents add a hydrophobic character, potentially limiting its solubility in highly polar solvents.
  • Temperature Impact: The solubility may also vary with temperature; increased temperature can generally enhance solubility in solvents.

In summary, 1,3-dibutylimidazolidin-2-one exhibits solubility primarily in polar and moderately polar solvents, yet its hydrophobic butyl groups introduce some complexity. Therefore, it is crucial for researchers and practitioners to consider both its structural characteristics and the choice of solvent for optimal solubility outcomes.

Interesting facts

Interesting Facts About 1,3-Dibutylimidazolidin-2-one

1,3-Dibutylimidazolidin-2-one is a fascinating compound within the imidazolidinone family, and it offers intriguing insights for chemists and students alike:

  • Structure and Stability: This compound features a five-membered ring structure containing two nitrogen atoms. The imidazolidinone structure contributes to its stability, making it an excellent candidate for various applications in pharmaceuticals and materials science.
  • Synthetic Utility: The synthesis of 1,3-dibutylimidazolidin-2-one showcases the versatility of imidazolidinones in organic chemistry. It can act as a building block for other complex molecules, demonstrating its importance in the development of new substances.
  • Biological Relevance: Compounds with imidazolidinone structures are often explored for their potential biological activities. Researchers are particularly interested in their efficacy in drug design, as they may interact with biological targets in beneficial ways.
  • Applications in Catalysis: There is growing interest in using imidazolidinones as catalysts in various chemical reactions. Their unique electronic properties can enhance reaction rates or selectivity in synthetic processes.
  • Research Horizons: As a relatively less-studied compound, 1,3-dibutylimidazolidin-2-one presents numerous opportunities for research. Future studies may unlock new applications or reveal innovative uses in different fields of science.

As emphasized by the quote, "The beauty of chemistry lies in its infinite potential and the mysteries waiting to be unraveled." Students and researchers exploring 1,3-dibutylimidazolidin-2-one may find themselves at the forefront of exciting discoveries that could shape future scientific advancements.

Synonyms
2-IMIDAZOLIDINONE, 1,3-DIBUTYL-
N,N'-Dibutylethyleneurea
4761-09-5
NSC-186243
1,3-dibutylimidazolidin-2-one
1,3-dibutyl-2-imidazolidinone
NSC186243
NSC 186243
BRN 0134228
K96R8SC3PU
2-Imidazolidinone,3-dibutyl-
SCHEMBL4424409
WLN: T5NVNTJ A4 C4
1,3-dibutyl-imidazolidin-2-one
DTXSID80197220
AKOS006278462
5-24-01-00061 (Beilstein Handbook Reference)