Skip to main content

Pyridostigmine bromide

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

At room temperature, pyridostigmine bromide is in a solid state, typically found in the form of a crystalline powder.

Melting point (Celsius)
153.00
Melting point (Kelvin)
426.15
Boiling point (Celsius)
402.00
Boiling point (Kelvin)
675.15
General information
Molecular weight
261.18g/mol
Molar mass
261.1770g/mol
Density
1.4300g/cm3
Appearence

Pyridostigmine bromide typically appears as a white or off-white crystalline powder. It is usually odorless and has a bitter taste.

Comment on solubility

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

The solubility of the compound (1-benzylpyridin-1-ium-3-yl) N,N-dimethylcarbamate bromide can be analyzed through various factors influencing its behavior in different solvents.

Key Factors Influencing Solubility:

  • Polarity: The compound features a quaternary ammonium structure, which typically enhances its solubility in polar solvents such as water due to ionic interactions.
  • Functional Groups: The presence of the carba-mate and bromide groups can contribute to solubility by participating in hydrogen bonding and ionic interactions.
  • Temperature: As with many chemical compounds, solubility may increase with temperature, helping to dissolve the compound in a solvent.

It is noteworthy that this compound is likely to exhibit:

  1. High solubility in polar organic solvents due to its ionic nature.
  2. Variable solubility in non-polar organic solvents, which may limit its use in certain chemical applications.

In summary, the solubility of (1-benzylpyridin-1-ium-3-yl) N,N-dimethylcarbamate bromide is influenced by its ionic structure and the surrounding solvent environment, making it pivotal for its practical application in various chemical reactions.

Interesting facts

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

This intriguing compound combines properties from both pyridine and carbamate structures, leading to a unique set of characteristics and applications. Here are some interesting highlights:

  • Cationic Nature: The presence of the benzylpyridin-1-ium moiety gives this molecule a positive charge, which plays a crucial role in its chemical behavior, particularly in catalytic and receptor activities.
  • Versatile Functionality: As a carbamate derivative, it can act as a versatile intermediary in organic synthesis. Carbamates are known for their ability to function as protecting groups and in the synthesis of pharmaceuticals.
  • Role in Medicinal Chemistry: Due to its unique structure, this compound may exhibit bioactive properties, potentially leading to interesting findings in drug development. Compounds similar to this structure have shown promise in treating various conditions.
  • Solvent Interactions: The bromide counterion may influence solubility and reactivity, which can be crucial in solvent interactions and the solubility of the resultant products in organic reactions.
  • Research Potential: Further studies could explore its applications in materials science, particularly in areas such as photonics, where ionic compounds often serve as active dopants or additives.

As with many compounds, exploring its potential in both academic research and industrial applications may yield surprising results, making this compound a worthy subject for future investigation. As scientists often say, "Chemistry is the study of matter, but really, it’s the study of change!"

Synonyms
BENZPYRINIUM BROMIDE
587-46-2
Benzostigmine
Bromure de benzpyrinium
Bromuro de benzopirinio
Benzpyrinii bromidum
Benzpyrinium bromide [INN]
Benzpyrinii bromidum [INN-Latin]
UNII-X0L78YB79M
Bromure de benzpyrinium [INN-French]
Bromuro de benzopirinio [INN-Spanish]
1-Benzyl-3-dimethylcarbamoyloxypyridinium bromide
X0L78YB79M
Benzpyrinium bromide [INN:NF]
1-Benzyl-3-hydroxypyridinium bromide dimethylcarbamate
Pyridinium, 1-benzyl-3-dimethylcarbamoyloxy-, bromide
Pyridinium, 1-benzyl-3-hydroxy-, bromide, dimethylcarbamate
BENZPYRINIUM BROMIDE [MI]
Pyridinium, 3-((dimethylaminocarbonyl)oxy)-1-(phenylmethyl)-, bromide
Benzpyrinii bromidum (INN-Latin)
Bromure de benzpyrinium (INN-French)
Bromuro de benzopirinio (INN-Spanish)
benzpyrinium (cation)
1-Benzyl-3-((dimethylcarbamoyl)oxy)pyridin-1-ium bromide
(1-benzylpyridin-1-ium-3-yl) N,N-dimethylcarbamate;bromide
1-benzyl-3-[(dimethylcarbamoyl)oxy]pyridin-1-ium bromide
SCHEMBL679368
CHEMBL2106108
DTXSID70974224
AKOS015899428
NS00122706
D84275
Q27293204