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Bis [2-(2-iodoacetyl)oxyethyl] methyl ammonium iodide

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Identification
Molecular formula
C10H21INO4
CAS number
37441-29-5
IUPAC name
bis[2-(2-iodoacetyl)oxyethyl]-methyl-ammonium;iodide
State
State

It exists as a solid at room temperature.

Melting point (Celsius)
230.00
Melting point (Kelvin)
503.15
Boiling point (Celsius)
380.00
Boiling point (Kelvin)
653.15
General information
Molecular weight
588.96g/mol
Molar mass
588.9600g/mol
Density
2.6800g/cm3
Appearence

Bis [2-(2-iodoacetyl)oxyethyl] methyl ammonium iodide typically appears as a white to off-white crystalline powder.

Comment on solubility

Solubility of bis[2-(2-iodoacetyl)oxyethyl]-methyl-ammonium;iodide

The solubility of bis[2-(2-iodoacetyl)oxyethyl]-methyl-ammonium;iodide can be influenced by various factors, including its ionic nature and the presence of functional groups. As a quaternary ammonium compound, it generally displays a good degree of solubility in polar solvents due to its ionic characteristics.

Key Points Influencing Solubility:

  • Polarity: The polar nature of the iodide ion enhances the compound's solubility in polar solvents like water.
  • Chain Length: The ethoxy groups may also contribute to the solubility profile, as shorter alkyl chains tend to be more soluble.
  • Concentration: As with many ionic compounds, increased concentration can lead to better solubility up to a certain point before saturation occurs.
  • Temperature: Higher temperatures generally improve solubility for many compounds; thus, heating might help dissolve this compound more effectively.

In summary, bis[2-(2-iodoacetyl)oxyethyl]-methyl-ammonium;iodide is expected to have notable solubility in polar solvents, making it a versatile compound for various applications in solution-based processes. As emphasized, understanding the effects of polarity, chain length, concentration, and temperature is crucial for predicting its behavior in different environments.

Interesting facts

Interesting Facts about bis[2-(2-iodoacetyl)oxyethyl]-methyl-ammonium;iodide

bis[2-(2-iodoacetyl)oxyethyl]-methyl-ammonium;iodide, often referred to in scientific literature through its abbreviation, represents a fascinating compound that combines multiple functional groups. Here are some intriguing aspects:

  • Unique Structure: The presence of both iodoacetyl and methylammonium groups endows this compound with a unique ability to participate in various chemical reactions, making it a valuable precursor in synthetic organic chemistry.
  • Biomedical Relevance: Compounds similar to this one often possess antibacterial and antifungal properties, primarily due to their ability to disrupt microbial membrane integrity, making them of interest in pharmacological research.
  • Versatile Uses: The potential applications of this compound extend to areas such as drug delivery systems and the development of advanced materials. The versatility of its functional groups allows it to be tailored for specific interactions in biochemical settings.
  • Synthetic Pathways: The synthesis of this compound often involves multi-step processes that could include reactions like nucleophilic substitution, making it a prime candidate for study in advanced organic chemistry courses.
  • Ion Exchange Properties: As an iodide salt, this compound can potentially act as a source of iodide ions in various chemical reactions, which may be crucial in certain organic synthesis pathways.

This compound serves as a striking example of how complex organic structures can lead to diverse functionalities, reflecting the rich interplay between chemical composition and behavior. Its study not only enhances our understanding of synthetic methodologies but also opens doors for innovations in materials science and medicine.

Synonyms
S 41
NSC 30030
ACETIC ACID, IODO-, DIESTER with METHYLDIETHANOLAMINE, HYDROIODIDE
N,N-Bis(2-(iodoacetoxy)ethyl)-N-methylamine hydriodide
N,N-Bis(2-(iodoacetoxy)ethyl)-N-methylamine hydroiodide
Acetic acid, iodo-, (methylimino)diethylene ester, hydriodide
Acetic acid, iodo-, diester with methyldiethanolamine, hydriodide