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Quinacrine

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Identification
Molecular formula
C23H30ClN3O2
CAS number
130-95-0
IUPAC name
dimethyl-(8-nitroacridin-1-yl)ammonium;chloride
State
State

At room temperature, Quinacrine is typically in a solid state. Its crystalline form means it is found as a solid powder, often used in various applications where its distinctive yellow color can be seen.

Melting point (Celsius)
210.00
Melting point (Kelvin)
483.15
Boiling point (Celsius)
240.00
Boiling point (Kelvin)
513.15
General information
Molecular weight
399.97g/mol
Molar mass
399.9150g/mol
Density
1.4000g/cm3
Appearence

Quinacrine hydrochloride, also known as Mepacrine, typically appears as a yellow crystalline powder. Its distinct color makes it easily identifiable. The powder is highly soluble in water, giving it a vibrant yellow solution.

Comment on solubility

Solubility of Dimethyl-(8-nitroacridin-1-yl)ammonium; Chloride

Dimethyl-(8-nitroacridin-1-yl)ammonium chloride is an intriguing compound when it comes to its solubility characteristics. Its solubility can be described as follows:

  • Water Solubility: This compound exhibits a notable solubility in polar solvents, particularly water. The presence of the ammonium group enhances its affinity for water, allowing it to dissolve quite readily.
  • Solvent Dependence: While it is soluble in water, the solubility might vary in other solvents. For instance, it could be less soluble in non-polar solvents due to its ionic nature.
  • Concentration Effects: At higher concentrations, the solubility might be reduced due to increased ion pairing and saturation limits.

In practical applications, the solubility of dimethyl-(8-nitroacridin-1-yl)ammonium chloride is a crucial factor that influences its usability in various chemical reactions and biological systems. As one may quote, "Solubility is key; it defines the path of chemical reactions." Understanding its solubility profile is essential for optimizing conditions in synthetic and analytical scenarios.

In summary, the solubility of dimethyl-(8-nitroacridin-1-yl)ammonium chloride largely reflects its ionic structure, making it a versatile compound in various chemical contexts.

Interesting facts

Interesting Facts about Dimethyl-(8-nitroacridin-1-yl)ammonium Chloride

Dimethyl-(8-nitroacridin-1-yl)ammonium chloride is a fascinating compound that merges **organic chemistry** with intricate applications in various scientific fields. Here are some intriguing insights:

  • Dual Functionality: This compound features both ammonium and nitro groups, allowing it to participate in diverse chemical reactions. Its structure enables it to act as both a nucleophile and an electrophile, which is essential in synthetic organic chemistry.
  • Fluorescence Properties: The acridinyl moiety is known for its strong fluorescence. This property makes derivatives of this compound particularly useful in biochemical assays and as tracers in biological systems.
  • Potential Applications: Compounds of this nature have been studied for their potential roles in drug development. Their ability to intercalate into DNA suggests possible uses in targeted therapies for cancer, highlighting their importance in medicinal chemistry.
  • Crystal Engineering: The study of this compound may also contribute to the field of crystal engineering. The interactions between the ammonium groups and chloride anions can lead to unique crystal lattice formations, whose studies may reveal new material properties.
  • Environmental Implications: As researchers strive to understand and mitigate pollution, the synthesis and breakdown of similar compounds can illuminate environmental pathways and their effects on ecosystems.

In summary, dimethyl-(8-nitroacridin-1-yl)ammonium chloride exemplifies the complexity and utility of synthetic organic compounds. Delving into its properties can unlock significant advances in both chemical research and applied sciences.

Synonyms
9-ACRIDINAMINE, N,N-DIMETHYL-1-NITRO-, HYDROCHLORIDE
RefChem:1074929
1-Nitro-9-(dimethylamino)-acridine hydrochloride
28743-45-5
dimethyl-(8-nitroacridin-1-yl)azanium;chloride
C 702