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propantel

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Identification
Molecular formula
C16H17N2O5 + I
CAS number
67681-26-1
IUPAC name
[6-isopropyl-3-methyl-2-(methylcarbamoyloxy)phenyl]-trimethyl-ammonium;iodide
State
State

Solid at room temperature

Melting point (Celsius)
182.00
Melting point (Kelvin)
455.00
Boiling point (Celsius)
210.00
Boiling point (Kelvin)
483.00
General information
Molecular weight
449.38g/mol
Molar mass
449.3750g/mol
Density
1.3300g/cm3
Appearence

White crystalline powder

Comment on solubility

Solubility of [6-isopropyl-3-methyl-2-(methylcarbamoyloxy)phenyl]-trimethyl-ammonium;iodide

The solubility of [6-isopropyl-3-methyl-2-(methylcarbamoyloxy)phenyl]-trimethyl-ammonium;iodide can be analyzed from several perspectives.

Factors Influencing Solubility:

  • Polarity: The presence of the trimethyl-ammonium group suggests that the compound is likely to be ionic and polar, which typically enhances solubility in polar solvents such as water.
  • Ion Formation: The iodide ion may increase solubility due to its ability to dissociate and interact favorably with solvent molecules.
  • Hydrophobic Portions: The isopropyl and methyl groups may introduce some hydrophobic character, potentially complicating solubility in very polar solvents.

In general, compounds similar to this structure often exhibit the following solubility properties:

  1. Highly soluble in water due to ionic character and polar functionality.
  2. Variable solubility in organic solvents, often tending to favor polar organic solvents.
  3. Potential challenges in solubility due to larger hydrophobic groups that could limit solubility in pure water.

In summary, while the trimethyl-ammonium;iodide part of the compound suggests a strong potential for solubility in polar media, the overall solubility behavior could be nuanced and require experimental validation for precise applications. Exploring the solubility conditions (like temperature and pH) will provide further insights into utilizing this complex compound effectively.

Interesting facts

Interesting Facts about [6-isopropyl-3-methyl-2-(methylcarbamoyloxy)phenyl]-trimethyl-ammonium;iodide

This intriguing compound displays a unique blend of organic and inorganic chemistry, showcasing the versatility of ammonium salts in various applications. It derives its name from a significant structural motif, combining elements that contribute to its functionality and behavior.

Key Features

  • Ammonium Ion: The presence of the trimethylammonium group is crucial, as it enhances solubility in polar solvents and promotes interactions with biological systems.
  • Functional Groups: The methylcarbamoyloxy substitution introduces bioactive properties, potentially acting as a catalyst in chemical reactions or as an intermediate in synthetic routes.
  • Isopropyl and Methyl Substituents: These groups can influence the compound's sterics and electronics, thereby affecting its reactivity and interaction with other molecules.

Moreover, this compound can be particularly studied for its potential biological implications, such as:

  • Investigations in medicinal chemistry, particularly in the design of drug delivery systems.
  • Research in agrochemicals, where its active components may exhibit herbicidal or fungicidal properties.
  • Utilization in studying ionic liquids, especially considering the iodide anion, which often imparts unique conductivity characteristics.

From a laboratory perspective, this compound serves as a potent reminder of how structural intricacies lead to diverse functionalities. As a chemist reflects on compounds like this, one is reminded of the pivotal quote: "Chemistry is the central science." It truly emphasizes how varied elements can lead to extraordinary compounds with broad applications.


Synonyms
Carbamic acid, methyl-, (5-trimethylammonio)carvacryl ester, iodide
18659-44-4
Ammonium, (6-(N-methylcarbamoyloxy)thymyl)trimethyl-, iodide
Carbamic acid, N-methyl-, 4-dimethylaminocarvacryl ester, methiodide
AMMONIUM, (6-HYDROXYTHYMYL)TRIMETHYL-, IODIDE, METHYLCARBAMATE
trimethyl-[3-methyl-2-(methylcarbamoyloxy)-6-propan-2-ylphenyl]azanium;iodide
SCHEMBL29393246