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Identification
Molecular formula
C48H74O14
CAS number
70288-86-7
IUPAC name
2-piperidin-1-ium-1-ylethyl N-(2,6-dichlorophenyl)carbamate;chloride
State
State

At room temperature, the compound exists as a solid.

Melting point (Celsius)
155.00
Melting point (Kelvin)
428.00
Boiling point (Celsius)
315.50
Boiling point (Kelvin)
588.50
General information
Molecular weight
875.10g/mol
Molar mass
875.1000g/mol
Density
1.3300g/cm3
Appearence
The compound appears as a white to off-white crystalline powder. It is commonly encountered in its pure form, which is colorless and odorless.
Comment on solubility

Solubility of 2-piperidin-1-ium-1-ylethyl N-(2,6-dichlorophenyl)carbamate;chloride

The solubility of 2-piperidin-1-ium-1-ylethyl N-(2,6-dichlorophenyl)carbamate;chloride can be influenced by various factors such as temperature, solvent type, and ionic strength. This compound, being a quaternary ammonium compound, is likely to display the following characteristics:

  • High Solubility in Water: Due to the presence of ionic groups, which interact favorably with polar water molecules, promoting dissolution.
  • Solvent Specificity: While it is soluble in water, the solubility in organic solvents may vary, so it is crucial to consider the solvent used for potential applications.
  • Temperature Effects: Increasing the temperature could enhance solubility, as it typically increases kinetic energy and disrupts molecular interactions.

Moreover, when discussing solubility, one can often refer to the concept of “like dissolves like”. This principle suggests that polar compounds mix well with polar solvents and non-polar compounds mix with non-polar solvents. In the case of this compound, its ionic nature aligns well with aqueous environments. Therefore, for practical applications, one can anticipate a favorable solubility profile in water-based formulations.

In conclusion, while the exact solubility may require empirical evaluation under specific conditions, the structural characteristics of the compound point toward a significant solubility in polar solvents, especially water.

Interesting facts

Interesting Facts about 2-Piperidin-1-ium-1-ylethyl N-(2,6-dichlorophenyl)carbamate; Chloride

This intriguing compound is a member of the carbamate family, which are known for their versatile applications in various fields including agriculture and pharmaceuticals. Here are some captivating insights into this compound:

  • Biological Activity: The structure of this compound hints at its potential biological activity, especially in the field of medicinal chemistry. Carbamates often exhibit interesting pharmacological properties, making them subjects of extensive research for drug development.
  • Chlorine Substitution: The presence of the 2,6-dichlorophenyl group in its structure contributes to the compound's lipophilicity and can enhance its ability to penetrate cell membranes, which is important for its biological function.
  • Applications: Inspired by commercial pesticides, carbamates are often designed for use as insecticides or herbicides, highlighting the compound’s potential utility in agriculture applications.
  • Ionic Nature: Being a chloride salt, this compound's ionic nature may influence its solubility and stability, which are critical factors in both laboratory synthesis and industrial applications.
  • Synthetic Pathways: The synthesis of such complex structures can be challenging and often involves multi-step reactions that require careful planning and execution, making it an interesting target for organic chemists.

With its versatile functionality and intriguing structure, this compound exemplifies the intersection between organic chemistry and practical applications in science. Further studies into its mechanisms of action could illuminate how modifications to its structure can enhance desired properties or reduce adverse effects.

Synonyms
2-Piperidinoethyl 2,6-dichlorocarbanilate hydrochloride
20228-95-9
K 485
2,6-Dichlorocarbanilic acid 2-piperidinoethyl ester hydrochloride
CARBANILIC ACID, 2,6-DICHLORO-, 2-PIPERIDINOETHYL ESTER, HYDROCHLORIDE