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Acriflavine hydrochloride

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Identification
Molecular formula
C13H11ClN3
CAS number
8063-24-9
IUPAC name
(6-aminoacridin-3-yl)ammonium;chloride
State
State
Solid at room temperature, usually presented in crystalline powder form.
Melting point (Celsius)
260.00
Melting point (Kelvin)
533.00
Boiling point (Celsius)
760.00
Boiling point (Kelvin)
1 033.00
General information
Molecular weight
301.80g/mol
Molar mass
301.8000g/mol
Density
1.2600g/cm3
Appearence

Acriflavine hydrochloride appears as an orange-red crystalline powder, typically utilized in its hydrochloride form for better solubility in water solutions. It is often used in microbiology and cell biology as a fluorescent dye and antiseptic.

Comment on solubility

Solubility of (6-aminoacridin-3-yl)ammonium Chloride

(6-aminoacridin-3-yl)ammonium chloride, with the chemical formula often represented as C13H13ClN2, is a compound that exhibits noteworthy solubility properties. Here are some key insights into its solubility characteristics:

  • The compound is typically considered to be soluble in polar solvents, such as water and alcohols.
  • Due to its ionic nature, the presence of the ammonium ion aids in its solubility. As a result, it tends to dissociate well in solution.
  • Specific solubility can be impacted by factors such as temperature and pH. For example, increased temperatures often enhance solubility.
  • It's important to note that while it can dissolve in water, the degree of solubility may vary and should be assessed through empirical testing.

In general, compounds with similar structures often display solubility trends that can be predicted based on their functional groups and molecular interactions. Thus, understanding the solubility of (6-aminoacridin-3-yl)ammonium chloride can be essential for various applications in both pharmaceuticals and chemical research.

Interesting facts

Interesting Facts about (6-aminoacridin-3-yl)ammonium chloride

(6-aminoacridin-3-yl)ammonium chloride is a fascinating compound with several important applications in the fields of chemistry and biology. Here are some key points to consider:

  • Fluorescent Properties: This compound exhibits unique fluorescent properties, making it valuable in various applications such as fluorescence microscopy and bioimaging.
  • Antimicrobial Activity: Studies have shown that (6-aminoacridin-3-yl)ammonium chloride possesses significant antimicrobial effects, which sparks interest for potential uses in medical treatments.
  • pH Sensitivity: The compound's properties can change significantly with varying pH levels, thus making it a candidate for pH-sensing applications.
  • Role in Research: In scientific research, this compound is often utilized as a fluorescent probe for studying various biological processes at the molecular level.
  • Potential Drug Development: Given its structural characteristics, (6-aminoacridin-3-yl)ammonium chloride has shown potential for development into pharmaceutical agents targeting specific biological pathways.

With its multifaceted functions, (6-aminoacridin-3-yl)ammonium chloride represents a significant area of interest for chemists and biologists alike. As one researcher aptly put it, "The interplay between its structural properties and biological activity opens up exciting avenues for exploration."

Future research may uncover even more uses or enhance its efficacy in existing applications. Connecting insights across disciplines could lead to breakthroughs in both chemical synthesis methods and biomedical innovations.