Skip to main content

Methylergometrine diiodide

ADVERTISEMENT
Identification
Molecular formula
C8H14N2I2
CAS number
6793-80-4
IUPAC name
trimethyl-[[5-(trimethylammonio)-1H-indol-3-yl]methyl]ammonium;diiodide
State
State

At room temperature, methylergometrine diiodide is typically in a solid state. The compound is usually stored in an airtight container to prevent iodine loss or coloration changes.

Melting point (Celsius)
190.00
Melting point (Kelvin)
463.15
Boiling point (Celsius)
200.00
Boiling point (Kelvin)
473.15
General information
Molecular weight
553.50g/mol
Molar mass
553.4900g/mol
Density
2.1000g/cm3
Appearence

Methylergometrine diiodide appears as a yellow to orange crystalline powder. This appearance is typical of many iodine-containing organics, which tend to have distinct coloration due to charge-transfer complexes formed in the solid state.

Comment on solubility

Solubility of Trimethyl-[[5-(trimethylammonio)-1H-indol-3-yl]methyl]ammonium; diiodide

The solubility of the compound trimethyl-[[5-(trimethylammonio)-1H-indol-3-yl]methyl]ammonium; diiodide, often referred to by its more common name, can be quite intriguing due to its unique chemical structure. Here are some key aspects regarding its solubility:

  • Water Solubility: This compound contains quaternary ammonium groups, which typically enhance its solubility in polar solvents such as water. The presence of iodide ions also suggests some degree of solubility due to their ionic nature.
  • Solvent Interaction: Solubility is influenced by the interactions with the solvent. The trimethylammonio group tends to create favorable interactions with water through hydrogen bonding, potentially increasing solubility.
  • Temperature Effects: Like many ionic compounds, its solubility may increase with rising temperature. This phenomenon is particularly important in applications requiring higher concentrations.
  • Concentration Limits: While it may be soluble in water, the *maximum concentration* can vary and is essential to determine in practical experiments to prevent precipitation.

Overall, understanding the solubility of this compound is crucial for its application in various chemical processes. As a general rule, compounds containing both ionic and polar covalent bonds tend to exhibit enhanced solubility in polar solvents, making this compound a *potentially useful* candidate for research and application.

Interesting facts

Interesting Facts about Trimethyl-[[5-(trimethylammonio)-1H-indol-3-yl]methyl]ammonium Diiodide

Trimethyl-[[5-(trimethylammonio)-1H-indol-3-yl]methyl]ammonium diiodide is a fascinating compound with intriguing properties and potential applications. Here are some notable points about this compound:

  • Quaternary Ammonium Compound: This compound features a quaternary ammonium structure, which is characterized by a positively charged nitrogen atom bonded to four organic groups. Such compounds play vital roles in various biological and chemical processes.
  • Indole Derivative: The presence of the indole ring, a core structure in many biologically active compounds, suggests that it may exhibit unique biological activities, including antimicrobial and anticancer properties.
  • Charge Properties: As a diiodide salt, it contains iodide ions that can influence its solubility and interaction with biological membranes. This feature can be crucial for drug delivery systems.
  • Potential Applications: Given its chemical structure, trimethyl-[[5-(trimethylammonio)-1H-indol-3-yl]methyl]ammonium diiodide could have implications in various fields, including pharmaceutical chemistry, biochemistry, and material science.
  • Research Interest: Researchers are often intrigued by quaternary ammonium compounds, as they can act as surfactants, disinfectants, and even ionic liquids, paving the way for innovative studies in chemical synthesis and formulations.

In summary, trimethyl-[[5-(trimethylammonio)-1H-indol-3-yl]methyl]ammonium diiodide not only demonstrates a unique chemical structure but also embodies the potential for exploration in scientific research and practical applications. The combination of its quaternary ammonium nature and indole framework make it a compound worthy of further study!

Synonyms
5-Dimethylaminogramine bis methiodide
AMMONIUM, TRIMETHYL(5-(TRIMETHYLAMMONIO)-3-INDOLYLMETHYL)-, DIIODIDE
6884-79-3
DTXSID90988545
N,N,N-Trimethyl-3-[(trimethylazaniumyl)methyl]-1H-indol-5-aminium diiodide