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Ivermectin

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Identification
Molecular formula
C48H74O14
CAS number
70288-86-7
IUPAC name
quinuclidin-3-yl N-(2-chloro-6-methyl-phenyl)carbamate
State
State

The compound is typically found in a solid state at room temperature. As a crystalloid powder, it maintains its integrity under standard laboratory conditions and does not exhibit volatility or fluidity that is associated with liquids or gases.

Melting point (Celsius)
155.00
Melting point (Kelvin)
428.00
Boiling point (Celsius)
530.00
Boiling point (Kelvin)
803.00
General information
Molecular weight
875.10g/mol
Molar mass
875.1040g/mol
Density
1.2300g/cm3
Appearence

Ivermectin generally appears as a white to off-white crystalloid powder. It is hydrophobic in nature, meaning it does not mix well with water, but it can dissolve in organic solvents such as ethanol and methanol. The compound does not have a significant odour.

Comment on solubility

Solubility of Quinuclidin-3-yl N-(2-chloro-6-methyl-phenyl)carbamate

Quinuclidin-3-yl N-(2-chloro-6-methyl-phenyl)carbamate, a complex organic compound, demonstrates specific solubility characteristics that are influenced by its molecular structure and functional groups. Understanding its solubility can be advantageous in various applications, particularly in pharmaceuticals and chemical processes.

Key Points on Solubility:

  • Water Solubility: This compound tends to have limited solubility in aqueous environments, which may affect its bioavailability and transport in biological systems.
  • Organic Solvents: It is generally more soluble in organic solvents such as ethanol or methanol. This is due to its hydrophobic aromatic rings and carbamate group.
  • Temperature Influence: Solubility can also vary with temperature; an increase in temperature might enhance solubility in organic solvents.
  • pH Sensitivity: The solubility may be pH-dependent, particularly due to the presence of the carbamate functional group, which can ionize in certain conditions.

Overall, it is essential to consider these factors when working with quinuclidin-3-yl N-(2-chloro-6-methyl-phenyl)carbamate in both laboratory and industrial contexts. As with all chemical compounds, a detailed understanding of solubility can aid in maximizing efficacy and minimizing environmental impact.

Interesting facts

Interesting Facts about Quinuclidin-3-yl N-(2-chloro-6-methyl-phenyl)carbamate

Quinuclidin-3-yl N-(2-chloro-6-methyl-phenyl)carbamate is a fascinating compound that occupies a unique place in the realm of medicinal chemistry. This compound is notable for several reasons:

  • Pharmacological Significance: Often explored for its potential therapeutic applications, this compound is part of a class of drugs that may influence neurological pathways, particularly in the treatment of conditions like Alzheimer’s disease.
  • Structural Features: The molecule features a quinuclidine core, which is a bicyclic amine. This structure is essential for its biological activity and provides unique properties compared to other compounds.
  • Synthetic Pathways: The synthesis of quinuclidin-3-yl N-(2-chloro-6-methyl-phenyl)carbamate can involve intricate multi-step processes, showcasing the creativity and strategic thinking involved in organic synthesis.
  • Research Applications: Researchers are continuously investigating the mechanisms of action and potential modifications to enhance its efficacy and reduce side effects, making it a dynamic area of study.

Quinuclidin-3-yl N-(2-chloro-6-methyl-phenyl)carbamate exemplifies the blend of chemistry and pharmacology, highlighting how structural modifications can lead to significant changes in biological activity. As the field of medicinal chemistry advances, compounds like this offer a glimpse into the future of drug development.

In the words of renowned chemist and innovator, "The beauty of chemistry lies in its ability to create diversity from simplicity." This compound certainly embodies that philosophy.