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Azinphos-ethyl

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Identification
Molecular formula
C12H21NO3PS2
CAS number
2642-71-9
IUPAC name
dipropoxyphosphinothioyl N,N-diethylcarbamodithioate;hydrogen sulfide
State
State

At room temperature, Azinphos-ethyl is in the solid state, often found in crystalline form.

Melting point (Celsius)
49.50
Melting point (Kelvin)
322.65
Boiling point (Celsius)
197.00
Boiling point (Kelvin)
470.15
General information
Molecular weight
317.34g/mol
Molar mass
317.3400g/mol
Density
1.2380g/cm3
Appearence

Azinphos methyl is typically a colorless to white crystal that can also appear as a beige powder. Its crystalline nature is notable under ambient conditions.

Comment on solubility

Solubility of Dipropoxyphosphinothioyl N,N-Diethylcarbamodithioate; Hydrogen Sulfide

The solubility behavior of dipropoxyphosphinothioyl N,N-diethylcarbamodithioate and its relation to hydrogen sulfide is quite intriguing due to the following factors:

  • Polarity: The presence of multiple functional groups may influence the overall polarity of the compound, impacting its solubility in different solvents.
  • Hydrogen Bonding: The potential for hydrogen bonding can enhance solubility in polar solvents, making it more soluble in substances like water or alcohols compared to non-polar solvents.
  • Complexation: Interactions between hydrogen sulfide and the functional groups can lead to the formation of complexes, which may modify the solubility characteristics.
  • pH Sensitivity: Variations in pH can affect the ionization of the compound, altering its solubility. Acidic or basic conditions may either enhance or inhibit dissolution.

It is important to note that temperature also plays a crucial role; typically, increased temperatures can increase solubility for many compounds. As researchers continue to investigate these interactions, a comprehensive understanding of solubility will better facilitate the use of this compound in various applications.

Interesting facts

Interesting Facts About Dipropoxyphosphinothioyl N,N-Diethylcarbamodithioate

Dipropoxyphosphinothioyl N,N-diethylcarbamodithioate, often recognized for its intriguing chemistry, is a compound featuring a unique blend of functionalities that position it as a significant compound in the realm of organophosphorus chemistry. Here are some noteworthy aspects:

  • Pioneering Applications: This compound serves as a vital intermediate in the synthesis of various phosphorus-containing molecules, many of which find applications in agriculture as pesticides or herbicides.
  • Phosphorus Chemistry: The presence of phosphorus in its structure is critical, as phosphorus compounds are known for their ability to form stable bonds with both organic and inorganic substances, leading to a variety of functionalities.
  • Thioesters in Biochemistry: The thioyl component of this compound contributes to its role in biochemical processes, specifically in the formation and breakdown of certain biological thioesters, which are pivotal in cellular metabolism.
  • Toxicological Aspects: Understanding the toxicology of this compound, especially in its interaction with biological systems, is crucial. It’s important to conduct rigorous assessments to ensure safety and mitigate risks in its applications.
  • Hydrogen Sulfide Awareness: The compound is linked with hydrogen sulfide, a notorious gas known for its characteristic smell of rotten eggs. Recognizing the implications of hydrogen sulfide is essential in both environmental sciences and chemical safety.

As a chemistry student or researcher, delving into the intricacies of dipropoxyphosphinothioyl N,N-diethylcarbamodithioate can lead to remarkable discoveries and innovations in both synthetic strategies and practical applications. Emphasizing its role in contemporary chemistry encourages a deeper appreciation for the interconnectedness of various chemical disciplines.

Synonyms
Compound 325
Holcomb compound 325
DTXSID30206997
O,O-Diisopropyl S-(diethylthiocarbamyl)thiothionophosphate hydrosulfide
5827-04-3
O,O-Diisopropyl-S-(diethylthiocarbamyl)phosphorodithioate hydrosulfide
DTXCID60129488