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Icaridin

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Identification
Molecular formula
C12H23ClN2O2
CAS number
119515-38-7
IUPAC name
2-piperidin-1-ium-1-ylethyl N-(5-chloro-2-methyl-phenyl)carbamate;chloride
State
State

At room temperature, Icaridin is in a liquid state. It remains stable and fluid under normal conditions.

Melting point (Celsius)
-5.00
Melting point (Kelvin)
268.15
Boiling point (Celsius)
296.00
Boiling point (Kelvin)
569.15
General information
Molecular weight
229.73g/mol
Molar mass
229.7330g/mol
Density
1.0460g/cm3
Appearence

Icaridin is a colorless, odorless liquid. It is typically clear and does not have a distinct color, making it visually similar to water.

Comment on solubility

Solubility of 2-piperidin-1-ium-1-ylethyl N-(5-chloro-2-methyl-phenyl)carbamate;chloride

The solubility of 2-piperidin-1-ium-1-ylethyl N-(5-chloro-2-methyl-phenyl)carbamate;chloride can be intriguing due to its unique molecular structure. The ionic nature of the compound suggests that it might display varying degrees of solubility in different solvents. Key points regarding its solubility include:

  • Water Solubility: Given that the compound contains a quaternary ammonium component, it is likely to exhibit good solubility in polar solvents such as water.
  • Organic Solvent Solubility: The presence of a chlorinated aromatic segment may enhance solubility in organic solvents like ethanol and acetone.
  • Temperature Dependence: Solubility can be influenced by temperature, generally increasing with higher temperatures.
  • pH Sensitivity: As an ionic compound, its solubility may also vary depending on the pH of the solution.

It is often noted that "the solubility of a compound can significantly impact its bioavailability and overall functionality." Thus, understanding the solubility of this particular compound can be crucial for applications in medicinal chemistry and related fields.


In summary, the solubility characteristics of 2-piperidin-1-ium-1-ylethyl N-(5-chloro-2-methyl-phenyl)carbamate;chloride suggest a favorable interaction with polar solvents while also permitting some degree of solubility in organic media, although further empirical studies would provide more definitive insights.

Interesting facts

Interesting Facts about 2-Piperidin-1-ium-1-ylethyl N-(5-chloro-2-methyl-phenyl)carbamate; chloride

This compound is a fascinating example of how intricate chemical structures can lead to a variety of applications, especially in the field of pharmaceuticals. Here are some interesting points to consider:

  • Pharmacological Potential: The presence of the piperidine group is often associated with compounds that exhibit remarkable biological activity. Many pharmaceutical drugs are derived from or inspired by piperidine structures due to their ability to interact effectively with biological targets.
  • Chlorine Influence: The 5-chloro substituent on the aromatic ring can significantly enhance the compound's lipophilicity, potentially improving its ability to cross biological membranes.
  • Biological Applications: Carbamates, such as the one featured in this compound, are known to play a role in the development of insecticides and herbicides, emphasizing the compound's relevance beyond medicinal chemistry.
  • Design Considerations: In drug design, the balance between hydrophilicity and lipophilicity is crucial. This compound’s structure suggests a careful design to ensure optimal solubility and bioavailability.
  • Mechanistic Insights: Compounds with carbamate moieties are often involved in enzyme inhibition studies, providing insights into metabolic pathways and the mechanisms of drug action.

As a chemistry student or scientist delving into this compound, it's important to appreciate how each functional group contributes to the overall properties and potential uses. It's not just about the structure but also about what that structure can achieve in real-world applications.


Synonyms
5-Chloro-2-methylcarbanilic acid 2-piperidinoethyl ester hydrochloride
20224-20-8
K 444
CARBANILIC ACID, 5-CHLORO-2-METHYL-, 2-PIPERIDINOETHYL ESTER, HYDROCHLORIDE