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Methylthiohypochlorite

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Identification
Molecular formula
CH3SCl
IUPAC name
chloromethanethioic S-acid
State
State
Methylthiohypochlorite is a liquid at room temperature.
Melting point (Celsius)
-40.00
Melting point (Kelvin)
233.15
Boiling point (Celsius)
30.00
Boiling point (Kelvin)
303.15
General information
Molecular weight
82.56g/mol
Molar mass
82.5560g/mol
Density
1.1475g/cm3
Appearence

Methylthiohypochlorite is typically found as a clear, colorless liquid.

Comment on solubility

Solubility of Chloromethanethioic S-acid

Chloromethanethioic S-acid presents intriguing characteristics regarding its solubility. Understanding its behavior in various solvents is crucial for both theoretical studies and practical applications. Here are some key points about its solubility:

  • Solvent Dependency: The solubility of chloromethanethioic S-acid can vary significantly depending on the solvent used. Common solvents include water and various organic solvents.
  • Aqueous Solubility: Generally, this compound has limited solubility in water due to its modest polarity. This can affect the compound’s use in aqueous environments.
  • Organic Solvents: Chloromethanethioic S-acid tends to exhibit higher solubility in organic solvents like alcohols and ethers, facilitating its applications in organic synthesis.
  • Temperature Effects: The solubility may also change with temperature; increased temperatures often enhance solubility for many chemicals.

It is important to note that solubility plays a critical role in determining the compound’s reactivity, stability, and bioavailability. As a result, understanding the solubility profile of chloromethanethioic S-acid is indispensable for researchers working with this intriguing compound.

Interesting facts

Interesting Facts about Chloromethanethioic S-acid

Chloromethanethioic S-acid, a notable member of the thioic acids family, presents a unique blend of chemical properties and potential applications. This compound is particularly interesting for several reasons:

  • Reactivity: This acid is highly reactive due to the presence of both the chloromethyl and thiol functional groups. This allows for various chemical transformations, making it a useful intermediate in organic synthesis.
  • Biological Importance: Compounds related to thioic acids play significant roles in biological systems as they can be involved in enzymatic processes or as potential drug candidates.
  • Industrial Applications: Chloromethanethioic S-acid is employed in the production of agrochemicals, pharmaceuticals, and dyes, reflecting its utility in various sectors.
  • Toxicity Considerations: As with many sulfur-containing compounds, it is important to handle Chloromethanethioic S-acid with care due to its potential toxicity and reaction hazards.
  • Synthesis: The synthesis of this acid can be achieved through various methods, often involving the introduction of sulfur-containing groups into chloromethyl derivatives.

As a chemistry student or scientist, understanding the intricacies of Chloromethanethioic S-acid can provide insights into both fundamental chemistry and practical applications. Its multifaceted nature allows for intriguing discussions pertaining to organic chemistry and material science.

In summary, Chloromethanethioic S-acid is not just another chemical compound; it embodies a significant aspect of chemical research and application, continually sparking curiosity within the scientific community.

Synonyms
CHLOROTHIOFORMIC ACID
FORMIC ACID, CHLOROTHIO-
Carbonochloridothioic acid
Chlorothiocarbonic acid
16890-85-0
carbonochloridothioic s-acid
DTXSID80937562