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Acridine Orange

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Identification
Molecular formula
C13H10N2O
CAS number
494-38-2
IUPAC name
9-amino-10H-acridin-3-one
State
State

Acridine Orange is in a solid state at room temperature.

Melting point (Celsius)
225.00
Melting point (Kelvin)
498.15
Boiling point (Celsius)
556.00
Boiling point (Kelvin)
829.15
General information
Molecular weight
222.27g/mol
Molar mass
222.2670g/mol
Density
0.5000g/cm3
Appearence

Acridine Orange appears as a solid with an orange to reddish appearance. It is commonly seen as a powder and is often used in laboratory settings as a dye. The color intensity may vary depending on the concentration and preparation method.

Comment on solubility

Solubility of 9-amino-10H-acridin-3-one

9-amino-10H-acridin-3-one, a compound with the chemical formula C13H10N2O, exhibits intriguing solubility characteristics that are vital for its applications in various fields, including pharmaceuticals and dyes.

In terms of solubility:

  • Solvent Polarity: Compounds similar to 9-amino-10H-acridin-3-one tend to show better solubility in polar organic solvents such as ethanol and dimethyl sulfoxide (DMSO).
  • pH Influence: The solubility can vary significantly with pH levels, as protonation of the amino group may enhance solubility in acidic conditions, making it more soluble in aqueous solutions.
  • Precipitation Potential: It can precipitate out of solution under certain conditions, emphasizing the need for careful control of solvent and concentration during experiments.

Moreover, temperature also plays a critical role in its solubility behavior; increased temperature generally improves solubility for many organic compounds.

In conclusion, understanding the solubility of 9-amino-10H-acridin-3-one is essential for optimizing its use in chemical processes and applications.

Interesting facts

Insights into 9-amino-10H-acridin-3-one

9-amino-10H-acridin-3-one is a fascinating compound notable for its unique structure and diverse applications in various fields. This compound is part of the acridine family, known for its distinctive aromatic ring system that contributes to its chemical reactivity. Here are some interesting attributes of 9-amino-10H-acridin-3-one:

  • Biological Significance: This compound has attracted attention for its potential as an antitumor agent. Several studies suggest that derivatives of acridine can effectively inhibit cancer cell proliferation.
  • Dye Chemistry: Owing to its vibrant and stable coloration, 9-amino-10H-acridin-3-one is often utilized in dyeing processes. It finds applications in various industries, especially in the manufacture of synthetic dyes.
  • Fluorescent Properties: Its fluorescence can be harnessed in analytical chemistry, providing insights into biomolecular interactions and helping in the development of advanced sensing technologies.
  • Intercalation Ability: This compound has the ability to intercalate into DNA, making it a subject of interest in studies of genetic material and its interactions with small molecules.

One particularly fascinating aspect of 9-amino-10H-acridin-3-one is its role in the synthesis of other chemical entities. The compound can serve as a precursor for various derivatives, which can lead to the development of new pharmaceutical agents with enhanced properties. As chemists explore the boundaries of this compound, they often quote its versatility in the laboratory:

"The beauty of 9-amino-10H-acridin-3-one lies not only in its structure but in its boundless possibilities."

In summary, 9-amino-10H-acridin-3-one is a compound that exemplifies the relationship between structure and function in chemistry. From medicinal chemistry to dye manufacturing, its applications are diverse and continually expanding, making it a noteworthy subject of study for chemists and researchers alike.