Skip to main content

1,3-dibutylisothiourea

ADVERTISEMENT
Identification
Molecular formula
C9H20N2S
CAS number
102-08-9
IUPAC name
1,3-dibutylisothiourea
State
State

At room temperature, 1,3-dibutylisothiourea is typically in a liquid state.

Melting point (Celsius)
-32.00
Melting point (Kelvin)
241.15
Boiling point (Celsius)
320.00
Boiling point (Kelvin)
593.15
General information
Molecular weight
188.33g/mol
Molar mass
188.3300g/mol
Density
0.9450g/cm3
Appearence

1,3-Dibutylisothiourea appears as a colorless to pale yellow liquid. It may have a faint characteristic odor typically associated with organic thioureas.

Comment on solubility

Solubility of 1,3-Dibutylisothiourea

1,3-Dibutylisothiourea, with its unique molecular structure, showcases notable solubility characteristics that can vary based on several factors. Here are some key points regarding its solubility:

  • Solvent Compatibility: This compound is generally soluble in polar solvents, such as water and alcohols, due to the presence of its isothiourea functional group.
  • Hydrophobic Interactions: The butyl groups contribute to hydrophobic interactions, which can decrease solubility in non-polar solvents.
  • Temperature Effect: Like many organic compounds, the solubility of 1,3-dibutylisothiourea can increase with temperature, making hot solvent systems more effective for dissolution.
  • pH Influence: The solubility may also be affected by the pH of the solution, particularly in acidic or basic conditions, where protonation or deprotonation can enhance solubility.

In summary, while 1,3-dibutylisothiourea exhibits good solubility in specific polar solvents, it is essential to consider the impact of temperature and pH on its solubility. As a result, it is crucial to conduct experiments in various solvents under controlled conditions to fully understand its solubility profile.

Interesting facts

Interesting Facts About 1,3-Dibutylisothiourea

1,3-Dibutylisothiourea is a fascinating compound with various applications and interesting characteristics that make it noteworthy in the field of chemistry.

Key Features

  • Structural Complexity: As a member of the isothiourea family, it features both thiourea and butyl groups, which contribute to its unique chemical properties.
  • Biological Activity: This compound has been studied for its potential antibacterial, antifungal, and herbicidal properties, showcasing its significance in both agricultural and pharmaceutical contexts.
  • Ligand Behavior: 1,3-Dibutylisothiourea can act as a ligand in coordination chemistry, forming complexes with various metal ions and thereby influencing their reactivity and stability.

Applications

Some notable applications include:

  • Research Tool: Often used in biochemical research to study enzyme activity and inhibition.
  • Agricultural Use: Being explored as a potential herbicide, contributing to the development of sustainable farming practices.
  • Coordination Complexes: Its ability to form stable complexes makes it valuable in material science and catalysis.

Safety and Handling

When working with 1,3-dibutylisothiourea, it is crucial to follow proper safety protocols. This includes:

  • Wearing appropriate personal protective equipment (PPE).
  • Utilizing fume hoods when handling this compound to minimize inhalation risks.
  • Proper disposal of chemical waste to prevent environmental contamination.

In conclusion, 1,3-dibutylisothiourea stands out as an intriguing compound that bridges the gap between organic chemistry and practical applications in various fields, underscoring the essential nature of chemical compounds in advancing both scientific knowledge and real-world solutions.