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Edrophonium Iodide

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Identification
Molecular formula
C5H16NO2.
I2.
C2H4NO3
CAS number
1890-54-8
IUPAC name
bis(2-hydroxyethyl)ammonium;2-(3,5-diiodo-4-oxo-1-pyridyl)acetate
State
State

At room temperature, Edrophonium Iodide is typically a solid crystalline substance. It is quite stable under normal storage conditions and is soluble in water.

Melting point (Celsius)
208.00
Melting point (Kelvin)
481.00
Boiling point (Celsius)
250.00
Boiling point (Kelvin)
523.00
General information
Molecular weight
615.96g/mol
Molar mass
615.9610g/mol
Density
2.1000g/cm3
Appearence

Edrophonium Iodide appears as a white to off-white crystalline powder. It is odorless and hygroscopic in nature. The exact color may vary slightly depending on purity and storage conditions.

Comment on solubility

Solubility of bis(2-hydroxyethyl)ammonium;2-(3,5-diiodo-4-oxo-1-pyridyl)acetate

The compound bis(2-hydroxyethyl)ammonium;2-(3,5-diiodo-4-oxo-1-pyridyl)acetate exhibits interesting solubility characteristics primarily attributed to its chemical structure.

  • Polarity: The presence of the ammonium group and two hydroxyethyl moieties enhances the compound's polarity, promoting solubility in polar solvents.
  • Solvent Compatibility: This compound is likely to be soluble in:
    • Water - due to hydrogen bonding capabilities
    • Alcohols - such as ethanol or methanol, which can stabilize the interacting groups
  • Influence of Iodine: The presence of diiodo groups, however, may affect solubility, making it less soluble in non-polar solvents.

In summary, while the solubility profile of this compound suggests a favorable interaction with polar solvents, the degree of solubility can vary based on concentration and temperature. As a general guideline, the compound is expected to be more soluble in aqueous solutions compared to organic solvents.

Interesting facts

Interesting Facts About Bis(2-hydroxyethyl)ammonium; 2-(3,5-diiodo-4-oxo-1-pyridyl)acetate

This fascinating compound, known as bis(2-hydroxyethyl)ammonium; 2-(3,5-diiodo-4-oxo-1-pyridyl)acetate, presents unique properties that make it notable in the field of chemistry. Here are some engaging aspects of this compound:

  • Versatile Applications: This compound has potential applications in pharmaceutical formulations and as a selective agent in biological studies due to its ability to interact with biological systems.
  • Structural Complexity: The incorporation of a pyridine ring, specifically a 3,5-diiodo-4-oxo group, indicates its role in various reactions, showcasing adaptability in synthetic pathways.
  • Hydroxyl Groups: The presence of two hydroxyethyl groups contributes to the compound's hydrophilicity, enabling it to function efficiently in aqueous environments.
  • Bioactivity Potential: Compounds of this nature often exhibit significant biological activity, including antimicrobial and anticancer properties, making them of great interest in medicinal chemistry.

As we delve into the nuances of this compound, it's important to understand its function in both synthetic and applied contexts. The combination of ammonium and pyridyl components typically enhances solubility and stability, which are crucial for various experimental applications.

In the words of renowned chemist Marie Curie, "Nothing in life is to be feared; it is only to be understood." Therefore, understanding the mechanisms and interactions of compounds like bis(2-hydroxyethyl)ammonium; 2-(3,5-diiodo-4-oxo-1-pyridyl)acetate is essential for advancing our knowledge and applications in modern chemistry.

Synonyms
Diodonum
Cardiotrastum
Neomethiodal
Diatrast
Iopyracil
Nosydrast
Nosylan
Oparenol
Pelviran
Pyelosil
Pylumbrin
Pyraceton
Umbradil
Uriodone
Vasiodone
Xumbradil
Savac
Neo-skiodan
Neo-tenebryl
Per-Abrodil
Per-Radiographol
Perjodol H
Ioduron B
Iodopyracet [NF]
Iodopiraceti [DCIT]
Diodonum [INN-Latin]
Diodona [INN-Spanish]
Iodopiraceti
EINECS 206-089-4
RP 3203
Diethanolamine 3,5-diiodo-4-pyridone-N-acetate
UNII-ZTK4026YJ5
Methylglucamine 3,5-diiodo-4-pyridone N-acetate
3,5-Diiodo-4-pyridone-N-acetic acid, diethanolamine salt
Bis(hydroxyethyl)ammonium 3,5-diiodo-4-pyridone-N-acetate
Diaethanolamin. 3,5-dijodpyridon-(4)-essigsaeure [German]
3,5-Diiodo-4-oxo-1(4H)pyridineacetic acid 2,2'-iminodiethanol salt
Ethanol, 2,2'-iminodi-, 3,5-diiodo-4-oxo-1(4H)-pyridineacetate (salt)
Diaethanolamin. 3,5-dijodpyridon-(4)-essigsaeure