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3-Methylacridin-9-amine

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Identification
Molecular formula
C14H12N2
CAS number
6315-15-3
IUPAC name
3-methylacridin-9-amine
State
State

At room temperature, 3-methylacridin-9-amine is typically found in a solid state, often as a crystalline powder.

Melting point (Celsius)
176.00
Melting point (Kelvin)
449.15
Boiling point (Celsius)
481.00
Boiling point (Kelvin)
754.15
General information
Molecular weight
208.27g/mol
Molar mass
194.2560g/mol
Density
1.2300g/cm3
Appearence

3-Methylacridin-9-amine is a solid compound, typically appearing as off-white or pale yellow crystalline powder. The intensity of color may vary slightly depending on the purity and specific processing methods used.

Comment on solubility

Solubility of 3-methylacridin-9-amine

The solubility of 3-methylacridin-9-amine can be notably influenced by various factors, including temperature, pH, and the solvent used. This compound exhibits moderate solubility in organic solvents and might be less soluble in water. Understanding its solubility characteristics is essential for applications in pharmaceuticals and organic synthesis.


Factors Affecting Solubility:

  • Temperature: Increased temperatures typically enhance the solubility of many organic compounds, including 3-methylacridin-9-amine.
  • Polarity of Solvent: Being largely nonpolar, this compound may dissolve better in nonpolar solvents such as chloroform or benzene compared to polar solvents like water.
  • pH Levels: Changes in pH can influence the ionization of the amine group, affecting solubility dynamics significantly.

As a rule of thumb, one can often remember that "like dissolves like," meaning nonpolar compounds are more readily soluble in nonpolar solvents. Therefore, researchers working with 3-methylacridin-9-amine should choose solvents carefully to optimize interactions and maximize solubility.

Interesting facts

Interesting Facts about 3-Methylacridin-9-amine

3-Methylacridin-9-amine is a fascinating compound that has captured the attention of researchers due to its unique structural properties and potential applications. Here are some intriguing aspects of this compound:

  • Structure and Features: The presence of both acridine and amine functionalities in 3-methylacridin-9-amine makes it a member of the acridine family, which are well-known for their diverse biological activities.
  • Biological Activity: Compounds containing acridine structures are often studied for their potential as therapeutic agents. Some derivatives have exhibited anticancer, antimicrobial, and anti-inflammatory properties.
  • Research Applications: 3-Methylacridin-9-amine is investigated in various fields such as medicinal chemistry and material science. Researchers are particularly interested in how small modifications to its structure can lead to significant changes in its biological effect.
  • Fluorescence Properties: Many acridine derivatives possess interesting fluorescence which can be exploited in biological imaging and sensing applications. This characteristic is particularly valuable in understanding cellular processes.
  • Chemical Synthesis: The synthesis of 3-methylacridin-9-amine can be a great educational exercise in organic chemistry, involving multi-step synthetic pathways that illustrate the principles of functionalization and ring transformation.

As a compound that bridges the worlds of synthesis, biology, and materials science, 3-methylacridin-9-amine continues to be a subject of inquiry for those looking to unlock its full potential. “The beauty of chemistry lies in its ability to transform basic elements into a multitude of applications that can influence our lives.”

Synonyms
ACRIDINE, 9-AMINO-3-METHYL-
BRN 0159422
23045-13-8
5-Amino-2-methylacridine (European)
DTXSID80177608
4-21-00-04256 (Beilstein Handbook Reference)
RefChem:317144
DTXCID00100099
9-amino-3-methylacridine
CHEMBL148238
SCHEMBL11055652