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Quinacrine

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Identification
Molecular formula
C23H30ClN3O
CAS number
83-89-6
IUPAC name
N6,N6,2-trimethylacridine-3,6-diamine
State
State

At room temperature, quinacrine is a solid.

Melting point (Celsius)
250.00
Melting point (Kelvin)
523.15
Boiling point (Celsius)
550.00
Boiling point (Kelvin)
823.15
General information
Molecular weight
401.96g/mol
Molar mass
401.9580g/mol
Density
1.2200g/cm3
Appearence

Quinacrine is typically seen as a yellow crystalline powder.

Comment on solubility

Solubility of N6,N6,2-trimethylacridine-3,6-diamine

The solubility of N6,N6,2-trimethylacridine-3,6-diamine in various solvents exhibits interesting characteristics that can be attributed to its molecular structure and functional groups. Here are some key points to consider:

  • Polarity Influence: The solubility of this compound largely depends on its charge distribution and polar functional groups within the molecule.
  • Solvent Compatibility: It is often more soluble in organic solvents such as ethanol or acetone due to hydrophobic interactions.
  • Water Solubility: Due to its organic nature, it has limited solubility in water, a common characteristic for compounds with similar structures.
  • Temperature Consideration: Solubility may enhance with temperature increases, highlighting the endothermic character of dissolving in non-polar solvents.

To summarize, N6,N6,2-trimethylacridine-3,6-diamine demonstrates nuanced solubility behavior influenced by various factors. As a rule of thumb, "like dissolves like," where organic solvents yield better solubility for this compound compared to polar solvents like water.

Interesting facts

Interesting Facts about N6,N6,2-Trimethylacridine-3,6-Diamine

N6,N6,2-trimethylacridine-3,6-diamine is an intriguing compound with a variety of applications and notable characteristics. Here are some engaging facts that highlight its significance:

  • Structural Complexity: The molecule showcases a unique structural motif due to its acridine core, which consists of a fused bicyclic system. This structure greatly influences its chemical behavior and reactivity.
  • Role in Synthesis: It serves as a useful intermediate in organic synthesis, particularly in the production of pharmaceuticals and agrochemicals. Its derivatives have been investigated for potential therapeutic applications.
  • Fluorescent Properties: The trimethyl groups attached to the acridine backbone contribute to its fluorescent properties, making it a candidate for applications in fluorescence microscopy and imaging techniques.
  • Biological Activity: Research indicates that compounds related to N6,N6,2-trimethylacridine-3,6-diamine may exhibit significant biological activity, such as antibacterial or antiviral effects, which opens avenues for developing new medicinal agents.
  • Research Interest: As a subject of academic investigation, this compound has been the focus of numerous studies exploring its properties and applications in various fields of chemistry.

In conclusion, N6,N6,2-trimethylacridine-3,6-diamine embodies a rich area of research potential and offers a glimpse into the fascinating intersection of structure and function in chemistry. As more studies reveal its properties, this compound may lead to notable advancements in both synthetic and applied chemistry.

Synonyms
Coriphosphine
Neutral Yellow
2-Methyl-3-amino-6-dimethylaminoacridine
BRN 0407236
N6,N6,2-Trimethyl-3,6-acridinediamine hydrochloride
3-Amino-6-(dimethylamino)-2-methylacridine
N(sup 6),N(sup 6),2-Trimethyl-3,6-acridinediamine
3,6-Acridinediamine, N(sup 6),N(sup 6),2-trimethyl-
ACRIDINE, 3-AMINO-6-(DIMETHYLAMINO)-2-METHYL-
N6,N6,2-trimethyl-3,6-acridinediamine.HCl
3,6-Acridinediamine, N(sup 6),N(sup 6),2-trimethyl-(9CI)
5153-57-1
6-N,6-N,2-trimethylacridine-3,6-diamine
N6,N6,2-Trimethylacridine-3,6-diamine
SCHEMBL6258725
DTXSID70965854
AKOS040751247
N6,N6,2-trimethyl-3,6-acridinediamine
2-methyl-3-amino-6-dimethylamino-acridine
DB-130431
N~6~,N~6~,2-Trimethylacridine-3,6-diamine