Acridine Orange Base

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Identification

Molecular formula
C23H27Cl3N3O
CAS Number
494-38-2
IUPAC Name
4-[(6-chloro-2-methoxy-acridin-9-yl)ammonio]pentyl-diethyl-ammonium;dichloride
Molecular Weight
394.77g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.1250g/cm3
Synonyms
SCHEMBL15061349
Interesting facts

Interesting Facts about 4-[(6-chloro-2-methoxy-acridin-9-yl)ammonio]pentyl-diethyl-ammonium; dichloride

The compound 4-[(6-chloro-2-methoxy-acridin-9-yl)ammonio]pentyl-diethyl-ammonium; dichloride is a remarkable example of a quaternary ammonium compound, reflecting the complexity and creativity of modern organic chemistry. Here are some intriguing aspects:

  • Versatile Applications: This compound is known for its promising role in pharmaceutical research, particularly in drug development and delivery systems. Its unique structure enables selective targeting of cellular components.
  • Fluorescent Properties: The acridine moiety within the compound exhibits interesting fluorescent properties, making it useful in labeling and imaging applications. This is particularly valuable in biomedical research for studying cellular processes.
  • Ion Exchange: As a quaternary ammonium salt, the dichloride form is capable of ion exchange, which can be utilized in various chemical reactions and processes, including catalysis and as a phase transfer catalyst.
  • Antibacterial Activity: Research has shown that derivatives of acridine possess antibacterial properties, suggesting that this compound might exhibit similar effects, opening avenues for new antimicrobial agents.
  • Structure-Activity Relationship: Investigating the structure-activity relationship (SAR) of such compounds can help chemists understand how modifications to its structure affect biological activity and interactions on a molecular level.

In conclusion, the compound 4-[(6-chloro-2-methoxy-acridin-9-yl)ammonio]pentyl-diethyl-ammonium; dichloride serves as a fascinating platform for research within organic and medicinal chemistry, illustrating the intersection of chemical structure and biological function.

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