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Thiacloprid

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Identification
Molecular formula
C10H9ClN4S
CAS number
111988-49-9
IUPAC name
[3-hydroxy-1-methyl-3,3-bis(3-thienyl)propyl]-methyl-dipropyl-ammonium
State
State

At room temperature, thiacloprid is typically in a solid state.

Melting point (Celsius)
136.00
Melting point (Kelvin)
409.00
Boiling point (Celsius)
380.00
Boiling point (Kelvin)
653.00
General information
Molecular weight
252.77g/mol
Molar mass
252.7700g/mol
Density
1.6300g/cm3
Appearence

Thiacloprid appears as a crystalline solid. It is usually colorless or white to beige in appearance.

Comment on solubility

Solubility of [3-hydroxy-1-methyl-3,3-bis(3-thienyl)propyl]-methyl-dipropyl-ammonium

This compound, with its complex structure, exhibits unique solubility characteristics. Generally, the solubility of such organic ammonium compounds can be influenced by several factors, including:

  • Polarity: The presence of hydroxyl groups typically enhances solubility in polar solvents such as water.
  • Hydrophobic interactions: The thienyl groups contribute hydrophobic interactions which can reduce solubility in aqueous environments.
  • Temperature: Increased temperature often leads to higher solubility for most organic compounds.
  • pH Levels: The ionization of ammonium groups can be pH-dependent, affecting solubility in various solutions.

In summary, the solubility of [3-hydroxy-1-methyl-3,3-bis(3-thienyl)propyl]-methyl-dipropyl-ammonium can be viewed as a balance between its hydrophilic and hydrophobic characteristics. As such, it may be more soluble in alcoholic solutions rather than pure water, depending on the specific environmental conditions. As always, empirical solubility testing is recommended to obtain precise information, as theoretical predictions may not account for all molecular interactions.

Interesting facts

Interesting Facts About [3-hydroxy-1-methyl-3,3-bis(3-thienyl)propyl]-methyl-dipropyl-ammonium

This compound is a fascinating example of organic ammonium derivatives, which are widely studied for their unique chemical properties and potential applications. Notably, the presence of thienyl groups in its structure gives it distinctive characteristics that could be exploited in various fields of research.

Key Features:

  • Molecular Diversity: The compound contains both hydroxyl and ammonium functional groups, which can impart unique solubility and reactivity profiles.
  • Potential Applications: Due to its ammonium nature, this compound may exhibit properties that are beneficial in pharmaceuticals, especially as:
    • Quaternary ammonium compounds are known for their antimicrobial properties.
    • Drug delivery systems, owing to their ability to interact with biological membranes.
  • Thienyl Influence: The thienyl moieties could enhance electronic properties, making this compound a subject of interest in organic electronics and as a possible candidate for semiconducting materials.

As reported in various scientific studies, compounds with a similar structure have shown efficacy in various biological applications, highlighting the importance of structure-activity relationships in drug design. Researchers suggest that the incorporation of thienyl rings can improve the pharmacological profile of related compounds.

In conclusion, [3-hydroxy-1-methyl-3,3-bis(3-thienyl)propyl]-methyl-dipropyl-ammonium not only exemplifies the intriguing complexity of chemical synthesis but also opens doors to innovative applications across multiple scientific domains. Its unique combination of functional groups sets it apart in the study of organic compounds.