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Dimeformate diiodide

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Identification
Molecular formula
C16H30N2O2I2
CAS number
125938-78-1
IUPAC name
4-methyl-4-[3-(2-methyl-1,3,3a,4,7,7a-hexahydroisoindol-2-ium-2-yl)propyl]morpholin-4-ium;diiodide
State
State

At room temperature, Dimeformate diiodide is a solid. This form makes it stable to handle under normal lab conditions, often used in experiments based on ionic interactions.

Melting point (Celsius)
183.00
Melting point (Kelvin)
456.00
Boiling point (Celsius)
300.00
Boiling point (Kelvin)
573.00
General information
Molecular weight
540.26g/mol
Molar mass
540.2550g/mol
Density
1.6758g/cm3
Appearence

Dimeformate diiodide appears as a crystalline solid with a pale yellow to off-white color. The compound is typically available in its solid form under ambient conditions, and it may appear as a powder or granules.

Comment on solubility

Solubility of 4-methyl-4-[3-(2-methyl-1,3,3a,4,7,7a-hexahydroisoindol-2-ium-2-yl)propyl]morpholin-4-ium;diiodide

The solubility of 4-methyl-4-[3-(2-methyl-1,3,3a,4,7,7a-hexahydroisoindol-2-ium-2-yl)propyl]morpholin-4-ium diiodide can be quite intriguing due to its complex structure. When considering its solubility, several factors come into play:

  • Polar Nature: Being a quaternary ammonium compound, it tends to be more soluble in polar solvents, particularly water.
  • Ionic Interaction: The presence of diiodide ions increases its solubility in polar solvents, facilitating interaction with water molecules.
  • Hydrogen Bonding: The morpholine ring in the compound can participate in hydrogen bonding, enhancing solubility in polar environments.

However, it is crucial to note that the overall solubility can also be affected by:

  • Temperature: Higher temperatures often increase solubility.
  • Concentration: In concentrated solutions, the solubility may decrease due to ion pairing.
  • Presence of Other Solutes: Other ions or solvents can impact the solubility through common ion effect or solvent competition.

In conclusion, while the compound shows promising solubility in polar solvents, specific conditions and interactions should be carefully considered to predict its behavior in various environments.

Interesting facts

Interesting Facts about 4-methyl-4-[3-(2-methyl-1,3,3a,4,7,7a-hexahydroisoindol-2-ium-2-yl)propyl]morpholin-4-ium;diiodide

This compound belongs to an exciting class of chemicals known as ionic liquids. Ionic liquids are salts that are liquid at room temperature and exhibit a variety of unique properties owing to their ionic nature. Here are some intriguing aspects of this compound:

  • Applications in Green Chemistry: Ionic liquids, including this compound, are often referred to as "green solvents" because they have low vapour pressures and can reduce volatile organic compound (VOC) emissions, making them environmentally friendly alternatives in various chemical processes.
  • Stability and Reactivity: The presence of a morpholine structure enhances the stability of the compound while providing potential sites for chemical reactivity. As a result, this compound can be utilized in organic synthesis and catalysis.
  • Biological Activity: Compounds with isoindole and morpholine functionalities can exhibit interesting biological activities, including potential therapeutic effects. The intricate structure suggests that it might interact with biological systems in unique ways, possibly influencing drug design.
  • Complex Formation: This compound's ability to form complexes with various anions opens avenues for its use in applications such as sensing and separation technologies, where specific ionic interactions may be harnessed.

As a scientist or chemistry student, exploring the myriad applications and properties of such complex compounds exemplifies the profound potential found in molecular design. The future of materials science and medicinal chemistry will be increasingly intertwined with compounds that harness such unique structures and properties.

Synonyms
2-Methyl-2-(3-(4-methyl-4-morpholinio)propyl)-3a,4,7,7a-tetrahydroisoindolinium diiodide
6309-71-3
8-(N-Methylmorpholiniumpropyl)-8-methyl-8-azoniumbicyclo-(4.3.0)-nonene-2 diiodide
NSC 41618
Isoindolinium, 3a,4,7,7a-tetrahydro-2-methyl-2-(3-(4-methyl-4-morpholinio)propyl)-, diiodide