Interesting facts
N-ethyladamantan-1-amine Hydrochloride
N-ethyladamantan-1-amine hydrochloride, often referred to in academic and research circles for its unique structure and potential applications, presents several compelling characteristics worth exploring:
- Structure and Stability: The compound is derived from adamantane, a polycyclic hydrocarbon, which contributes to its unique three-dimensional structure. This stability is pivotal in its interactions with biological systems.
- Biological Relevance: N-ethyladamantan-1-amine hydrochloride has garnered attention in medicinal chemistry, particularly for its possible neuroprotective benefits. Research suggests that it may influence neurotransmitter systems, making it a candidate for further studies in cognitive enhancement and neuroprotection.
- Analytical Methods: Due to its structural complexity, various analytical techniques such as NMR spectroscopy and mass spectrometry are utilized to study its properties and behavior. These methods aid in the precise characterization needed for pharmaceutical applications.
- Research Applications: The compound is often investigated for its potential in treating neurological disorders. Studies are ongoing to elucidate its mechanisms of action, as well as its efficacy and safety profiles.
- Inspirational Engineering: The design of adamantane-derived compounds illustrates the importance of molecular architecture in drug design—where modifying functional groups can lead to significant changes in activity and selectivity.
- Quote to Consider: As chemist and philosopher Isaac Asimov once said, “The saddest aspect of life right now is that science gathers knowledge faster than society gathers wisdom.” This underscores the importance of rigorous research into compounds like N-ethyladamantan-1-amine hydrochloride as we advance in medicinal science.
In summary, N-ethyladamantan-1-amine hydrochloride stands as a testament to the intricate nature of chemical compounds and their potential impacts. Its exploration not only furthers our understanding of pharmaceutical chemistry but also emphasizes the ongoing dialogue between structure and function in biological systems.
Synonyms
3717-42-8
1-(N-Ethylamine)adamantanamine hydrochloride
NSC 527916
1-ADAMANTANAMINE, N-ETHYL-, HYDROCHLORIDE
DTXSID00190652
DTXCID40113143
N-ethyladamantan-1-amine hydrochloride
1-(1-Aminoethyltricyclo-(3,3,1,1)[3,7]-decane)hydrochloride
N-ethyladamantan-1-amine;hydrochloride
MFCD01674015
SCHEMBL4433215
adamantayl ethylamine hydrochloride
N-ethyladamantan-1-aminehydrochloride
NSC527916
AKOS015894571
NSC-527916
DS-012506
CS-0307667
EN300-04474
G57915
F3052-0022
Z361993930
Tricyclo[3.3.1.13,7]decan-1-amine,n-ethyl-, hydrochloride (1:1)
Solubility of N-ethyladamantan-1-amine Hydrochloride
N-ethyladamantan-1-amine hydrochloride is a compound that displays intriguing solubility characteristics. Understanding its solubility profile is essential for various applications, whether in pharmaceutical or industrial contexts.
Key Solubility Insights:
It is noteworthy to mention that the solubility can vary significantly depending on the pH of the solution; thus, when dissolved in acidic conditions, N-ethyladamantan-1-amine hydrochloride remains highly soluble. However, in neutral or basic environments, its solubility might decrease due to the formation of less soluble free amine forms.
In Conclusion:
The solubility behavior of N-ethyladamantan-1-amine hydrochloride can be summarized as highly soluble in water and influenced by the temperature and pH of the solvent. Understanding these factors is crucial for optimizing its use in various applications.