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Pyridostigmine bromide

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Identification
Molecular formula
C15H20BrN2O2
CAS number
101-26-8
IUPAC name
(1-benzylpyridin-1-ium-3-yl) N,N-dimethylcarbamate
State
State

At room temperature, pyridostigmine bromide exists as a solid.

Melting point (Celsius)
153.50
Melting point (Kelvin)
426.70
Boiling point (Celsius)
77.60
Boiling point (Kelvin)
350.80
General information
Molecular weight
261.21g/mol
Molar mass
261.2110g/mol
Density
1.4000g/cm3
Appearence

Pyridostigmine bromide appears as a white crystalline powder. It is generally odorless.

Comment on solubility

Solubility of (1-benzylpyridin-1-ium-3-yl) N,N-dimethylcarbamate

The solubility of (1-benzylpyridin-1-ium-3-yl) N,N-dimethylcarbamate can be quite fascinating due to its unique structure. This compound, characterized by the presence of a pyridinium moiety, may exhibit varying solubility in different solvents.

  • Polar solvents: Compounds with pyridinium structures typically show good solubility in polar solvents such as water and methanol, primarily due to ionic interactions and hydrogen bonding.
  • Non-polar solvents: Conversely, in less polar environments, such as hexane or toluene, the solubility may significantly decrease. This is due to the inability of the ionic or polar character of the compound to interact favorably with the non-polar solvents.
  • Temperature effects: The solubility could also vary with temperature; generally, an increase in temperature can lead to increased solubility in most solvents.

As with many chemical compounds, the solubility of (1-benzylpyridin-1-ium-3-yl) N,N-dimethylcarbamate is influenced by both structural characteristics and the nature of the solvent. Understanding these factors is crucial for applications in fields ranging from pharmacology to materials science.

Interesting facts

Interesting Facts about (1-benzylpyridin-1-ium-3-yl) N,N-dimethylcarbamate

(1-benzylpyridin-1-ium-3-yl) N,N-dimethylcarbamate is a fascinating compound that exhibits intriguing properties and potential applications in various fields. Here are some compelling aspects worth noting:

  • Quaternary Ammonium Salt: This compound belongs to the class of quaternary ammonium salts, which play essential roles in biochemistry and pharmaceuticals.
  • Bioactivity: Compounds with a pyridinium structure are often associated with significant biological activities, potentially serving as agents against microbial infections or as therapeutic agents.
  • Modular Synthesis: The synthesis of this compound can be approached through modular strategies, allowing chemists to create a variety of analogs with tailored properties for specific applications.
  • Charge Properties: As a quaternary ammonium compound, it carries a positive charge, influencing its interaction with biological membranes and enhancing its ability to penetrate cellular barriers.
  • Stability & Reactivity: The N,N-dimethyl carbamate moiety provides stability while also making the compound reactive, which can be advantageous in drug formulations.

This compound is not only remarkable for its functionalities but also for its potential to inspire further research and innovation in fields such as medicinal chemistry, agriculture, and materials science. As we continue to explore these kinds of compounds, we may unlock new pathways for creating effective drugs and sustaining our environment.

In the words of Sir Isaac Newton, “What we know is a drop, what we don’t know is an ocean.” Through the study of compounds like (1-benzylpyridin-1-ium-3-yl) N,N-dimethylcarbamate, we are continually expanding that ocean of knowledge.

Synonyms
Benzpyrinium
Benzpyrinium ion
Benzpyrinium cation
UNII-P00DM5T7ZS
P00DM5T7ZS
1-Benzyl-3-hydroxypyridinium dimethylcarbamate
701897-98-5
DTXSID80220461
PYRIDINIUM, 3-(((DIMETHYLAMINO)CARBONYL)OXY)-1-(PHENYLMETHYL)-
DTXCID80142952
SCHEMBL2111654
CHEMBL2110802
Q27285944