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N3,N3,N6,N6-tetramethyl-9-phenyl-acridine-3,6-diamine

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Identification
Molecular formula
C22H22N4
CAS number
191019-84-2
IUPAC name
N3,N3,N6,N6-tetramethyl-9-phenyl-acridine-3,6-diamine
State
State

At room temperature, it exists in a solid state.

Melting point (Celsius)
202.00
Melting point (Kelvin)
475.15
Boiling point (Celsius)
569.20
Boiling point (Kelvin)
842.40
General information
Molecular weight
340.45g/mol
Molar mass
340.4450g/mol
Density
1.2110g/cm3
Appearence

This compound is typically found in the form of a crystalline solid, often characterized by its orange-yellow color.

Comment on solubility

Solubility of N3,N3,N6,N6-tetramethyl-9-phenyl-acridine-3,6-diamine

N3,N3,N6,N6-tetramethyl-9-phenyl-acridine-3,6-diamine is a complex organic compound whose solubility is influenced by various factors. Despite being a nitrogen-rich compound, the degree to which it dissolves in different solvents can vary significantly. Here are some key points regarding its solubility:

  • Polar Solvents: The presence of multiple amine groups can enhance solubility in polar solvents such as water or methanol, though due to steric hindrance, complete solubility may not be achieved.
  • Non-Polar Solvents: Conversely, its bulky hydrophobic phenyl group may promote better solubility in non-polar solvents like chloroform or toluene, showcasing hydrophobic interactions.
  • pH Impact: The solubility of this compound may also be affected by the pH of the solvent, with higher solubility typically observed in acidic conditions where amine groups can become protonated.
  • Temperature Effects: As is common with many organic compounds, increasing the temperature often increases solubility as it helps to overcome intermolecular forces.

Understanding the solubility behavior of N3,N3,N6,N6-tetramethyl-9-phenyl-acridine-3,6-diamine is crucial for applications in fields such as organic chemistry and material science. As with many similar compounds, “the design of new solvents tailored for optimum solubility can lead to breakthrough applications in synthesis and formulation”.

Interesting facts

Interesting Facts about N3,N3,N6,N6-tetramethyl-9-phenyl-acridine-3,6-diamine

N3,N3,N6,N6-tetramethyl-9-phenyl-acridine-3,6-diamine is a fascinating compound that finds its applications in various fields of chemistry and material science. Here are some compelling aspects to consider:

  • Fluorescent Properties: This compound exhibits unique fluorescent characteristics due to its acridine structure, making it valuable in the field of fluorescent probes and markers.
  • Role in Organic Light Emitting Diodes (OLEDs): With its capacity to efficiently emit light, it plays a role in enhancing the performance of OLEDs, which are crucial for modern display technologies.
  • Stability and Reactivity: Its structural features impart both stability and versatility, allowing chemists to modify the compound for various applications without significantly altering its fundamental properties.
  • Biological Activity: Preliminary studies suggest that derivatives of this compound may have potential biological activity, opening avenues for research in medicinal chemistry.

In the words of a prominent chemist, *“Compounds like N3,N3,N6,N6-tetramethyl-9-phenyl-acridine-3,6-diamine illustrate the beauty and intricacies of molecular design in the pursuit of innovation.”* This encapsulates the spirit of research surrounding such compounds.

The interplay of its chemical properties not only makes it a subject of study but also a stepping stone for advancements in technology and medicine. The ongoing exploration into its capabilities ensures that it remains a significant topic of discussion in scientific discourse.

Synonyms
ACRIDINE, 3,6-BIS(DIMETHYLAMINO)-9-PHENYL-
16292-14-1
BRN 0030164
3,6-Bis(dimethylamino)-9-phenylacridine
0-22-00-00490 (Beilstein Handbook Reference)
DTXSID80167488