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Icaridin

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Identification
Molecular formula
C12H23NO2
CAS number
119515-38-7
IUPAC name
2-piperidin-1-ium-1-ylethyl N-(2,5-dichlorophenyl)carbamate;chloride
State
State

At room temperature, Icaridin is typically in a liquid state.

Melting point (Celsius)
-40.00
Melting point (Kelvin)
233.15
Boiling point (Celsius)
296.00
Boiling point (Kelvin)
569.15
General information
Molecular weight
229.31g/mol
Molar mass
229.2040g/mol
Density
0.9907g/cm3
Appearence

Icaridin appears as a clear, colorless to light yellow liquid at room temperature.

Comment on solubility

Solubility of 2-piperidin-1-ium-1-ylethyl N-(2,5-dichlorophenyl)carbamate;chloride

The solubility of the compound 2-piperidin-1-ium-1-ylethyl N-(2,5-dichlorophenyl)carbamate;chloride can be largely influenced by its ionic nature and molecular structure. As a salt, this compound is expected to exhibit good solubility in polar solvents, primarily due to the interactions between its ionic parts and the solvent molecules. Several factors can significantly affect its solubility:

  • Polarity: The presence of charged groups within the molecule generally enhances solubility in water and other polar solvents.
  • Hydrogen Bonding: The ability of the compound to form hydrogen bonds with solvents can increase its solubility further.
  • Molecular Size: Larger molecular sizes may lead to decreased solubility due to steric hindrance.
  • Temperature: Increasing temperature can often improve solubility by providing energy that helps break intermolecular interactions.

It’s important to note that while this compound may dissolve well in water, it may exhibit different solubility characteristics in organic solvents. Hence, conducting solubility tests in various solvents could offer deeper insights. Overall, the solubility profile of this compound is a vital characteristic that impacts its applications and efficacy in various chemical processes.

Interesting facts

Interesting Facts about 2-Piperidin-1-ium-1-ylethyl N-(2,5-dichlorophenyl)carbamate;chloride

This compound is a fascinating example of a quaternary ammonium salt that showcases the intricate relationship between structure and function in chemistry. Here are some key points that highlight its importance:

  • Biological Relevance: The presence of the piperidinium ion in this compound indicates potential biological activity, particularly in the field of pharmacology. Compounds with piperidine moieties are often studied for their effects on neurotransmitter systems.
  • Insecticide Properties: The dichlorophenyl group is known to enhance the potency of compounds as insecticides. This specific structure can help target pests effectively, providing a means to manage agricultural challenges.
  • Carbamate Connection: Carbamates are widely recognized for their use in pesticides and pharmaceuticals. The incorporation of a carbamate group suggests this compound could exhibit both protective and therapeutic properties.
  • Synthetic Pathways: The synthesis of such compounds often involves sophisticated organic chemistry techniques. Understanding these mechanisms can equip chemists with valuable insights into designing new molecules with desirable properties.
  • Environmental Impact: The study of quaternary ammonium compounds is crucial in evaluating their environmental footprint. Research on their degradation and potential ecological effects helps support sustainable practices in chemical manufacturing.

As we delve deeper into the world of chemical compounds, 2-piperidin-1-ium-1-ylethyl N-(2,5-dichlorophenyl)carbamate;chloride exemplifies how structural design influences both function and application. Its diverse implications across biological and environmental realms make it a remarkable topic of study.


Synonyms
2-Piperidinoethyl 2,5-dichlorocarbanilate hydrochloride
20228-92-6
K 482
2,5-Dichlorocarbanilic acid 2-piperidinoethyl ester hydrochloride
CARBANILIC ACID, 2,5-DICHLORO-, 2-PIPERIDINOETHYL ESTER, HYDROCHLORIDE