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ethacridine lactate

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Identification
Molecular formula
C12H17ClN4O
CAS number
55965-09-4
IUPAC name
[N'-[N'-(4-ethoxyphenyl)carbamimidoyl]carbamimidoyl]ammonium;chloride
State
State

It is generally in a solid state at room temperature.

Melting point (Celsius)
220.00
Melting point (Kelvin)
493.15
Boiling point (Celsius)
276.00
Boiling point (Kelvin)
549.15
General information
Molecular weight
226.68g/mol
Molar mass
226.6800g/mol
Density
1.4900g/cm3
Appearence

The compound typically appears as a yellow crystalline solid.

Comment on solubility

Solubility of N'-[N'-(4-ethoxyphenyl)carbamimidoyl]carbamimidoyl]ammonium;chloride

The solubility of the compound N'-[N'-(4-ethoxyphenyl)carbamimidoyl]carbamimidoyl]ammonium;chloride can be influenced by several factors. Here are some key aspects to consider:

  • Polarity: The presence of both ammonium and chloride ions suggests that this compound may exhibit a degree of ionic character, possibly leading to improved solubility in polar solvents such as water.
  • Temperature Dependence: As with many ionic compounds, solubility can increase with temperature, indicating that higher temperatures might enhance the dissolution process.
  • Functional Groups: The ethoxy group (–O–C2H5) may impart some degree of non-polar character, which could affect solubility in organic solvents.
  • Concentration Effects: At high concentrations, the solubility limit may be reached, leading to the formation of a precipitate.

In summary, while N'-[N'-(4-ethoxyphenyl)carbamimidoyl]carbamimidoyl]ammonium;chloride is likely soluble in polar solvents, the specific conditions such as solvent choice, temperature, and concentration must be considered for optimal solubility results. As a general rule, it's recommended to conduct experimental solubility tests in varying conditions to fully understand the behavior of this compound.

Interesting facts

Exploring N'-[N'-(4-ethoxyphenyl)carbamimidoyl]carbamimidoyl ammonium chloride

N'-[N'-(4-ethoxyphenyl)carbamimidoyl]carbamimidoyl ammonium chloride is a fascinating compound that belongs to a class of chemicals known for their diverse applications in biological and medicinal chemistry. Here are some intriguing facts that highlight its significance:

  • Pharmaceutical Potential: This compound's unique structure may confer specific biological activities, making it a candidate for development as a pharmaceutical agent. Researchers are continually exploring similar compounds for their efficacy against various diseases.
  • Structural Complexity: The presence of the ethoxyphenyl group introduces interesting steric and electronic properties, which can influence the compound's reactivity and interactions with other molecules.
  • Versatile Functional Groups: The carbamimidoyl functionality is notable for its ability to participate in various chemical reactions, including those related to the synthesis of complex organic molecules.
  • Research Applications: Its unique properties make this compound a valuable tool in chemical synthesis and research, especially in the fields of biochemistry and organic synthesis.

This compound exemplifies the continuous effort in chemistry to discover molecules with unique properties and applications. As one researcher eloquently stated, "The most exciting discoveries often lie at the intersection of structure and function." Thus, compounds like N'-[N'-(4-ethoxyphenyl)carbamimidoyl]carbamimidoyl ammonium chloride are crucial to expanding our understanding of molecular chemistry.