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Methidathion

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Identification
Molecular formula
C6H11NNaOS5
CAS number
950-37-8
IUPAC name
sodium;N-(2-phenylethyl)-1-sulfanyl-methanimidothioate
State
State

At room temperature, Methidathion is typically in a solid state. It is handled under controlled conditions due to its volatility and potential for vapor emission at elevated temperatures.

Melting point (Celsius)
39.00
Melting point (Kelvin)
312.15
Boiling point (Celsius)
300.00
Boiling point (Kelvin)
573.15
General information
Molecular weight
302.39g/mol
Molar mass
302.3890g/mol
Density
1.2551g/cm3
Appearence

Methidathion typically appears as colorless or yellowish crystals. It is often found in the form of a solid substance that may have a slick or waxy appearance. Given its chemical nature, it is handled carefully due to its use as an insecticide.

Comment on solubility

Solubility of Sodium N-(2-phenylethyl)-1-sulfanyl-methanimidothioate

The solubility of sodium N-(2-phenylethyl)-1-sulfanyl-methanimidothioate is influenced by several key factors. Understanding its solubility properties can help in various applications, especially in pharmaceuticals and agricultural chemistry.

Key Factors Influencing Solubility:

  • Polarity: As a sodium salt, the compound has ionic characteristics, which often enhances its solubility in polar solvents, including water.
  • Temperature: Like most compounds, increased temperature can lead to increased solubility due to enhanced molecular motion.
  • pH Levels: The solubility could be affected by the pH of the solution, where changes in pH can impact the ionic state of the compound, therefore altering its solubility.
  • Interactions: Potential interactions with other ions or molecules in solution can either aid or hinder solubility.

In general, **sodium salts** are typically more soluble than their corresponding organic acids due to the stabilization of ions in aqueous solution. However, the presence of the phenyl group and sulfanyl moieties in this compound may impart unique challenges in solubility. As a result, a careful examination through solubility testing is recommended to determine its practical applications in various environments.

In summary, understanding the solubility of sodium N-(2-phenylethyl)-1-sulfanyl-methanimidothioate necessitates considering its ionic nature, the influence of environmental conditions, and its structural components.

Interesting facts

Interesting Facts about Sodium N-(2-phenylethyl)-1-sulfanyl-methanimidothioate

Sodium N-(2-phenylethyl)-1-sulfanyl-methanimidothioate is a fascinating compound that showcases a blend of organic chemistry with medicinal applications. Here are some intriguing insights about this compound:

  • Unique Structure: This compound contains a phenyl group, adding aromatic characteristics that may influence its reactivity and interactions with biological systems.
  • Potential Applications: It has been studied for its potential use in pharmaceuticals, particularly in drug formulation and development, due to its thiol moiety which can participate in various biochemical reactions.
  • Biochemical Interactions: The presence of sulfanyl and thioate groups in its structure suggests that this compound might play a role in redox reactions, which are crucial in cellular processes.
  • Research Focus: Ongoing research into compounds like this one can lead to advancements in therapeutics, particularly in areas related to neuropharmacology and anti-inflammatory treatments.
  • Synthesis Importance: The synthesis of this compound might employ various strategies including nucleophilic substitutions, and exploring these methods can expand the toolkit of synthetic chemists.

Overall, the exploration of sodium N-(2-phenylethyl)-1-sulfanyl-methanimidothioate not only enriches our understanding of its chemical properties but also broadens the horizon for future research in medicinal chemistry.