Succinylcholine chloride
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- Molecular formula
- C14H30Cl2N2O4
- CAS Number
- 71-27-2
- IUPAC Name
- diethyl-[2-(2-hydroxy-2,2-diphenyl-acetyl)oxyethyl]-methyl-ammonium;bromide
- Molecular Weight
- 290.74g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.3673g/cm3
- Synonyms
- methylbenactyzium bromide
Identification
Interesting facts
Interesting Facts about Diethyl-[2-(2-hydroxy-2,2-diphenyl-acetyl)oxyethyl]-methyl-ammonium Bromide
Diethyl-[2-(2-hydroxy-2,2-diphenyl-acetyl)oxyethyl]-methyl-ammonium bromide is a fascinating compound, often studied for its unique properties and applications in various fields. Here are some noteworthy aspects of this chemical:
- Quaternary Ammonium Compound: This compound belongs to a class of quaternary ammonium compounds, which are known for their effectiveness as surfactants and disinfectants. These features make them essential in both pharmaceuticals and industrial applications.
- Biological Relevance: The presence of a hydroxy group (–OH) in its structure suggests potential interactions with biological macromolecules, opening doors for research in drug delivery systems and therapeutic applications.
- Structure-Activity Relationship (SAR): The complex structure of this compound allows for the exploration of its pharmacokinetics. The diphenylacetyl moiety could enhance lipophilicity, influencing how the compound interacts within biological environments.
- Research Potential: Due to its intricate molecular design, this compound serves as a valuable subject for studies in organic synthesis and medicinal chemistry. Its ability to incorporate different functional groups can lead to novel derivatives with varied properties.
- Applications in Industry: Beyond pharmaceuticals, the structural characteristics of this compound may allow its use in emulsifiers, stabilizers, and as an ingredient in personal care products, leveraging its surfactant properties.
As a compound with myriad applications, Diethyl-[2-(2-hydroxy-2,2-diphenyl-acetyl)oxyethyl]-methyl-ammonium bromide exemplifies the importance of chemical diversity in advancing both scientific research and technological innovation. It challenges chemists to unlock its full potential, making it a compelling subject for ongoing study.