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O-butyl butoxycarbothioylsulfanylmethanethioate

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Identification
Molecular formula
C9H17O3S2
CAS number
108-32-7
IUPAC name
O-butyl butoxycarbothioylsulfanylmethanethioate
State
State

At room temperature, O-butyl butoxycarbothioylsulfanylmethanethioate is in a liquid state.

Melting point (Celsius)
-24.00
Melting point (Kelvin)
249.15
Boiling point (Celsius)
263.00
Boiling point (Kelvin)
536.15
General information
Molecular weight
222.36g/mol
Molar mass
222.3600g/mol
Density
1.0142g/cm3
Appearence

O-butyl butoxycarbothioylsulfanylmethanethioate is typically a colorless to pale yellow liquid. It has a characteristic odor and may appear slightly viscous.

Comment on solubility

Solubility of O-butyl butoxycarbothioylsulfanylmethanethioate

O-butyl butoxycarbothioylsulfanylmethanethioate is a complex compound with unique solubility characteristics. Understanding its solubility is essential for various applications in chemical synthesis and formulation. Below are some key aspects regarding this compound's solubility:

  • Solvent Type: This compound typically demonstrates varying solubility depending on the solvent used. It is generally more soluble in organic solvents such as alcohols, ethers, and aromatic hydrocarbons.
  • Temperature Influence: The solubility tends to increase with greater temperatures, which can aid in dissolution processes. Elevated temperatures can help to achieve a complete solution, enhancing the compound’s usability.
  • Effect of pH: The solubility may also be influenced by the pH of the solution, particularly if the solvent is aqueous. Variations in acidity or basicity can lead to changes in the ionization state of the compound.
  • Viscosity and Concentration: The solubility can be affected by the viscosity of the solution and the concentration of the compound itself; higher concentrations may lead to saturation and precipitation.

In summary, the solubility of O-butyl butoxycarbothioylsulfanylmethanethioate is dependent on various factors including solvent choice, temperature, pH, and concentration. Understanding these parameters is crucial for optimizing its use in chemical applications.

Interesting facts

Interesting Facts about O-butyl butoxycarbothioylsulfanylmethanethioate

O-butyl butoxycarbothioylsulfanylmethanethioate is a fascinating compound that showcases the complexity and diversity of chemical synthesis. Here are several intriguing facts about this remarkable compound:

  • Functional Groups Galore: This compound contains multiple functional groups, including thioates and ether functionalities, which contribute to its chemical reactivity and versatility.
  • Applications in Agriculture: O-butyl butoxycarbothioylsulfanylmethanethioate is a chemical of interest in the field of agrochemicals, potentially serving as a pesticide or herbicide due to its unique structure which can interact with biological systems.
  • Synthetic Pathways: The synthesis of this compound involves several steps, typically starting from readily available precursors and requiring careful optimization of reaction conditions to ensure high yields and purity.
  • Environmental Considerations: As with many synthetic chemicals, understanding the environmental impact of this compound is crucial. Studying its degradation and persistence in various ecosystems helps in assessing its safety and sustainability.
  • Potential Research Avenues: Researchers are continually exploring compounds like O-butyl butoxycarbothioylsulfanylmethanethioate for new applications, including their potential role in medicinal chemistry and materials science.

In the world of chemistry, compounds such as O-butyl butoxycarbothioylsulfanylmethanethioate embody the blend of creativity and science, pushing the boundaries of what we know about molecules and their functionalities. This highlights the importance of innovative thinking in the pursuit of new solutions to existing challenges.

Synonyms
Butylxanthogenic acid thioanhydride
Xanthic acid, butyl-, anhydrosulfide ester
4092-75-5
BRN 1783911
CARBONIC ACID, DITHIO-, ANHYDROSULFIDE, O,O-DIBUTYL ESTER
Formic acid, thiobis(thio-, O,O-dibutyl ester
DTXSID80193924
3-03-00-00349 (Beilstein Handbook Reference)
DTXCID20116415