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O-butyl benzylsulfanylmethanethioate

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Identification
Molecular formula
C12H16OS2
CAS number
104376-60-7
IUPAC name
O-butyl benzylsulfanylmethanethioate
State
State

At room temperature, o-butyl benzylsulfanylmethanethioate is typically in a liquid state. Its clear to pale-yellow hue and fluid consistency align with many organic thioesters. It is often stored in airtight containers to prevent oxidation and degradation.

Melting point (Celsius)
-10.00
Melting point (Kelvin)
263.15
Boiling point (Celsius)
331.00
Boiling point (Kelvin)
604.15
General information
Molecular weight
272.46g/mol
Molar mass
272.4600g/mol
Density
1.2000g/cm3
Appearence

O-butyl benzylsulfanylmethanethioate typically appears as a clear to pale yellow liquid, which can sometimes exhibit a faint aromatic odor characteristic of thioesters.

Comment on solubility

Solubility of O-butyl benzylsulfanylmethanethioate

O-butyl benzylsulfanylmethanethioate, a compound with intriguing properties, exhibits notable solubility characteristics that are essential for its applications. Understanding its solubility behavior is key for effective usage in various chemical processes. Here are some key points to consider:

  • Solvent Compatibility: This compound is typically soluble in organic solvents, such as ethanol and acetone, while showing limited solubility in polar solvents like water.
  • Influence of Temperature: As with many organic compounds, solubility tends to increase with temperature. Heating the solvent can enhance dissolution rates significantly.
  • Concentration Effects: At higher concentrations, the solubility can lead to saturation, impacting the reactivity and behavior of the compound in solutions.
  • Structural Impact: The bulky butyl and benzyl groups can hinder intermolecular interactions in water, thereby promoting solubility in non-polar or weakly polar environments.

To summarize, the solubility of O-butyl benzylsulfanylmethanethioate is primarily influenced by its molecular structure and the nature of the solvent. It is imperative to choose the appropriate solvent and conditions for effective usage:

"The key to unlocking the potential of O-butyl benzylsulfanylmethanethioate lies in understanding its solubility dynamics!"

In conclusion, while this compound may struggle to dissolve in water, it finds its strengths in compatible organic solvents, making it a fascinating subject of study in the realm of chemical compounds.

Interesting facts

Interesting Facts about O-butyl benzylsulfanylmethanethioate

O-butyl benzylsulfanylmethanethioate is a fascinating compound that captures the attention of chemists and researchers alike. Here are some engaging facts about this unique chemical:

  • Functional Versatility: This compound contains both a benzyl group and a thioate functional group, which makes it an intriguing subject for studying the properties and behaviors of organosulfur compounds.
  • Applications: O-butyl benzylsulfanylmethanethioate is often explored for its potential use in:
    • Pesticides as a potential biochemical agent
    • Pharmaceuticals, showcasing possible therapeutic applications
    • Flavor and fragrance chemistry, owing to the aromatic nature of its structure
  • Synthesis Challenges: The synthesis of this compound can be quite complex, often requiring careful manipulation of reaction conditions to ensure high yields and minimal side products. The manipulation of sulfur chemistry in reactions can be particularly intricate!
  • Safety Considerations: As with many sulfur-containing compounds, appropriate safety measures are essential. Proper handling and storage are critical to avoid adverse reactions, particularly in the presence of oxidizing agents.
  • Research Potential: Scientists are continuously investigating the properties of O-butyl benzylsulfanylmethanethioate, leading to insights into related compounds and their behaviors. The study of its reactivity and potential derivatives could unlock new avenues in material sciences and medicinal chemistry.

As research into O-butyl benzylsulfanylmethanethioate expands, it has the potential to contribute significantly to various fields, driven by its unique sulfur-centric structure and versatile applications. With ongoing advancements, who knows what remarkable discoveries await?

Synonyms
O-n-Butyl-S-benzyl-xanthate
5902-92-1
O-n-Butyl benzylxanthate
Thompson-hayward T-H103-M
Thioanhydride of butyl xanthogenic acid
O-Butyl S-(phenylmethyl)carbonodithioate
TH 103-M
Xanthic acid, butyl-, benzyl ester
ENT 27,190
AI3-27190
Carbonodithioic acid, O-butyl S-(phenylmethyl) ester
CARBONIC ACID, DITHIO-, S-BENZYL O-BUTYL ESTER
DTXSID10207780
DTXCID60130271
Carbonodithioic acid, O-butyl S-(phenylmethyl) ester (9CI)
O-butyl benzylsulfanylmethanethioate
O-Butyl phenylmethylsulfanylmethanethioate