Interesting facts
Interesting Facts about (2-phenoxyethylamino)ammonium chloride
(2-phenoxyethylamino)ammonium chloride is a fascinating compound that straddles the line between organic and inorganic chemistry. As a quaternary ammonium salt, it has gained attention in various fields of research, particularly in medicinal chemistry and agriculture. Here are some key points about this intriguing compound:
- Biological Significance: This compound has implications in drug design, particularly for its potential as a pharmaceutical agent. The structural features of phenoxyethylamine often contribute to biological activity.
- Surface-active Properties: As an ammonium salt, it exhibits surfactant characteristics, making it useful in formulations where emulsification is crucial, such as in cosmetic or pharmaceutical products.
- Research Applications: Studies have explored its role in enhancing drug delivery systems. Its ability to interact with cellular membranes makes it a candidate for improving the bioavailability of certain drugs.
- Stability and Reactivity: The stability of (2-phenoxyethylamino)ammonium chloride under various conditions can vary, which is vital for chemists to consider when utilizing this compound in different environments.
- Ion Interaction: Being a salt, it plays a role in ionic interactions that can affect solubility and reactivity in biological systems.
In summary, (2-phenoxyethylamino)ammonium chloride is not just a simple compound; it is a multifaceted entity with numerous applications and implications in scientific research. As one scientist aptly put it, "The study of such compounds paves the way for understanding complex biological systems and developing innovative therapeutic strategies."
Synonyms
HYDRAZINE, (2-PHENOXYETHYL)-, HYDROCHLORIDE
(2-phenoxyethylamino)azanium;chloride
Solubility of (2-phenoxyethylamino)ammonium chloride
(2-phenoxyethylamino)ammonium chloride, with the chemical formula (C8H11ClN2O), exhibits interesting solubility characteristics. This compound is generally soluble in polar solvents, such as water, due to its ability to form hydrogen bonds. Here are some key points regarding its solubility:
Considering its structure, the phenoxy moiety introduces a degree of hydrophobicity, which may limit solubility to some extent. However, its primary ionic nature dominates in polar circumstances, driving its dissolution in aqueous environments, a crucial characteristic for its applications.
Therefore, in practical terms, (2-phenoxyethylamino)ammonium chloride is a soluble compound with potential for various chemical uses, particularly in aqueous systems where its solubility can be fully utilized.