Pentamethylacridinium iodide
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- Molecular formula
- C22H28N2
- CAS Number
- 29558-62-3
- IUPAC Name
- N3,N3,N6,N6,10-pentamethylacridin-10-ium-3,6-diamine
- Molecular Weight
- 258.38g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.2100g/cm3
- Synonyms
- 21629-01-6
Identification
Interesting facts
Introduction to N3,N3,N6,N6,10-pentamethylacridin-10-ium-3,6-diamine
N3,N3,N6,N6,10-pentamethylacridin-10-ium-3,6-diamine is a fascinating compound that belongs to the class of acridine derivatives, known for their unique properties and applications in various fields, including biochemistry and molecular biology.
Interesting Facts
- Structure and Stability: The presence of multiple methyl groups contributes to the compound's stability and affects its electronic properties. This makes it an interesting subject for studying structure-activity relationships.
- Biological Activity: Acridine derivatives, including this compound, are often researched for their biological activity, particularly as potential anti-cancer agents. Their ability to intercalate with DNA makes them valuable in the development of therapeutic agents.
- Fluorescent Properties: Many acridine compounds exhibit fluorescence, allowing them to be used as effective markers in fluorescence microscopy. Researchers utilize this property to visualize biological samples, enhancing our understanding of cellular processes.
- Applications in Molecular Probes: Due to its distinct chemical properties, N3,N3,N6,N6,10-pentamethylacridin-10-ium-3,6-diamine can be employed as a molecular probe in various experimental setups. This can include studying protein-DNA interactions or tracking cellular changes.
In summary, N3,N3,N6,N6,10-pentamethylacridin-10-ium-3,6-diamine stands out not only for its intriguing structure but also for its contributions to the fields of medicinal chemistry and biochemistry. The ongoing research on compounds like this offers exciting possibilities for developing advanced materials and therapies.