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9-Methylacridine-3,6-diamine

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Identification
Molecular formula
C14H14N2
CAS number
120-78-5
IUPAC name
9-methylacridine-3,6-diamine
State
State
At room temperature, 9-Methylacridine-3,6-diamine is a solid. It exists in a crystalline form, typically with a yellow coloration, which is common for many aromatic compounds with extended conjugation.
Melting point (Celsius)
123.00
Melting point (Kelvin)
396.15
Boiling point (Celsius)
424.00
Boiling point (Kelvin)
697.15
General information
Molecular weight
222.28g/mol
Molar mass
222.2790g/mol
Density
1.2460g/cm3
Appearence
9-Methylacridine-3,6-diamine typically appears as a yellow crystalline solid. The crystalline nature and color may vary depending on the purity and specific conditions of its preparation.
Comment on solubility

Solubility of 9-methylacridine-3,6-diamine

9-methylacridine-3,6-diamine is a complex organic compound that exhibits unique solubility characteristics. While detailed solubility data can sometimes be sparse, it is generally understood that the solubility of such aromatic amines can vary significantly based on the solvent used and the environmental conditions. Key points to consider include:

  • Solvent Polarity: Aromatic compounds, including 9-methylacridine-3,6-diamine, tend to be more soluble in organic solvents such as ethanol, dimethyl sulfoxide (DMSO), and acetone compared to polar solvents like water.
  • Hydrogen Bonding: The presence of amino groups may facilitate hydrogen bonding with solvents, enhancing solubility in polar organic solvents.
  • Temperature Effects: Increasing temperature usually increases solubility for most compounds due to enhanced molecular movement.
  • pH Dependence: The solubility can also be influenced by the pH of the solution, particularly due to the amino groups that can either accept or donate protons.

It is often observed that compounds similar to 9-methylacridine-3,6-diamine are sparingly soluble in water, with effective solubility increasing in more organic environments.

In summary, solubility is a multifaceted characteristic and can be best evaluated using a combination of factors including solvent choice, temperature, and intrinsic chemical properties of the compound itself. An understanding of these elements provides a clearer view of how 9-methylacridine-3,6-diamine behaves in various environments.

Interesting facts

Interesting Facts About 9-Methylacridine-3,6-Diamine

9-Methylacridine-3,6-diamine, an intriguing compound belonging to the acridine family, has garnered interest in various fields due to its unique chemical properties and potential applications. Here are some notable highlights:

  • Chemical Structure: This compound features a methyl group at the 9-position and amino groups at the 3 and 6 positions of the acridine ring, which contributes to its reactivity and solubility characteristics.
  • Fluorescent Properties: Compounds like 9-methylacridine-3,6-diamine often exhibit interesting fluorescence properties, making them candidates for use in fluorescent dyes and labels in biological imaging.
  • Potential Applications: Its structure suggests potential applications in material science, particularly in the development of organic semiconductors and light-emitting devices.
  • Biological Activity: Some derivatives of acridine compounds have been noted for their antibacterial, antifungal, and even anticancer properties, which could open avenues for pharmaceutical exploration.
  • Synthesis: The syntheses of aromatic amines like 9-methylacridine-3,6-diamine involve multi-step processes that require careful control of reaction conditions to ensure desired outcomes.

In summary, 9-methylacridine-3,6-diamine is a compound with promising attributes that could be leveraged in various scientific fields. As chemists continue to explore its properties, we may discover even more applications that can benefit from this compound’s unique characteristics.

Synonyms
Acridine, 3,6-diamino-9-methyl-
18960-46-8
3,6-Diamino-9-methylacridine
DTXSID80172370