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Mepacrine hydrochloride

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Identification
Molecular formula
C23H30ClN+
CAS number
69-05-6
IUPAC name
methyl-[3-(2-tricyclo[9.4.0.03,8]pentadeca-1(15),3,5,7,9,11,13-heptaenyl)propyl]ammonium;chloride
State
State

At room temperature, mepacrine hydrochloride exists as a solid. It is stable under normal conditions and has applications primarily in the medical and scientific fields.

Melting point (Celsius)
225.00
Melting point (Kelvin)
498.15
Boiling point (Celsius)
312.00
Boiling point (Kelvin)
585.15
General information
Molecular weight
397.96g/mol
Molar mass
397.9600g/mol
Density
1.2070g/cm3
Appearence

Mepacrine hydrochloride is typically a yellow solid that may appear in powder form. Due to its coloration, it stands out and can fluoresce under specific conditions, adding to its visibility in certain applications.

Comment on solubility

Solubility of Methyl-[3-(2-tricyclo[9.4.0.03,8]pentadeca-1(15),3,5,7,9,11,13-heptaenyl)propyl]ammonium;chloride

The solubility of methyl-[3-(2-tricyclo[9.4.0.03,8]pentadeca-1(15),3,5,7,9,11,13-heptaenyl)propyl]ammonium;chloride is an intriguing subject, particularly due to its complex structure. While several factors influence the overall solubility of a compound, the unique characteristics of this ammonium salt provide a fascinating perspective:

  • Polarity: The presence of the ammonium group typically enhances solubility in polar solvents like water. However, the large hydrophobic tricyclic portion may hinder it.
  • Ionization: Being a chloride salt, it dissociates into methyl-[3-(2-tricyclo[9.4.0.03,8]pentadeca-1(15),3,5,7,9,11,13-heptaenyl)propyl]ammonium+ and Cl- ions in solution, which can promote solubility in water.
  • Temperature Dependency: As with many salts, solubility may increase with temperature, allowing more of the compound to dissolve in water at elevated temperatures.

Based on these observations, it can be said that while methyl-[3-(2-tricyclo[9.4.0.03,8]pentadeca-1(15),3,5,7,9,11,13-heptaenyl)propyl]ammonium;chloride may show moderate solubility in polar solvents, the large structural components must be taken into account, potentially resulting in a low overall solubility profile under standard conditions. This compound serves as a good illustration of the delicate balance influencing solubility, where molecular structure and ionization interplay significantly.

Interesting facts

Exploring Methyl-[3-(2-tricyclo[9.4.0.03,8]pentadeca-1(15),3,5,7,9,11,13-heptaenyl)propyl]ammonium Chloride

This fascinating compound, often recognized for its unique structural complexity, has captured the attention of chemists and researchers alike. Here are some compelling facts that showcase its remarkable characteristics:

  • Unique Structure: The compound features a tricyclic structure, which includes a highly intricate arrangement of fused carbon rings. This configuration may contribute to its reactivity and potential applications in various fields.
  • Biological Relevance: Compounds with ammonium groups, such as this one, are often studied for their interactions within biological systems. They can play a vital role in neurochemistry and pharmacology.
  • Potential Applications: Given its unique composition, this compound may exhibit properties valuable in drug design or materials science, potentially providing novel approaches in these areas.
  • Synthetic pathways: The synthesis of tricyclic compounds can offer insights into organic chemistry methodologies, including cyclization reactions and the manipulation of multiple reaction mechanisms.
  • Research Opportunities: The complexity of this molecule offers many avenues for exploration, from studying its physical properties to investigating its interactions with other chemical species.

In summary, methyl-[3-(2-tricyclo[9.4.0.03,8]pentadeca-1(15),3,5,7,9,11,13-heptaenyl)propyl]ammonium chloride is more than just a complex name; it is a gateway to understanding the interplay of structure, function, and potential applications in modern chemistry. As researchers uncover more about this compound, it could lead to significant advancements in both theoretical studies and practical applications.

Synonyms
methyl-[3-(2-tricyclo[9.4.0.03,8]pentadeca-1(15),3,5,7,9,11,13-heptaenyl)propyl]azanium;chloride