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Methyl Yellow

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Identification
Molecular formula
C14H15N4·2HCl
CAS number
60-11-7
IUPAC name
[N'-[1-[4-[[amino-[[amino(azaniumyl)methylene]amino]methylene]amino]phenyl]ethylideneamino]carbamimidoyl]ammonium;dichloride
State
State
At room temperature, Methyl Yellow is typically found in a solid state as a crystalline powder.
Melting point (Celsius)
240.00
Melting point (Kelvin)
513.00
Boiling point (Celsius)
580.00
Boiling point (Kelvin)
853.00
General information
Molecular weight
305.22g/mol
Molar mass
305.2150g/mol
Density
1.3000g/cm3
Appearence

Methyl Yellow appears as a bright yellow powder. It is typically used as a pH indicator and exhibits a distinct yellow color in its functional form.

Comment on solubility

Solubility of N'-[1-[4-[[amino-[[amino(azaniumyl)methylene]amino]methylene]amino]phenyl]ethylideneamino]carbamimidoyl]ammonium;dichloride

The solubility of N'-[1-[4-[[amino-[[amino(azaniumyl)methylene]amino]methylene]amino]phenyl]ethylideneamino]carbamimidoyl]ammonium;dichloride can be influenced by several factors due to its complex molecular structure. Understanding its solubility properties is crucial for applications in various fields including medicinal chemistry and biochemistry.

Factors Affecting Solubility

  • Ionic Nature: As a dichloride salt, the presence of chloride ions typically increases solubility in polar solvents like water.
  • Functional Groups: The numerous amino groups (-NH2) suggest potential interactions with water molecules, contributing to hydrophilicity.
  • Temperature: Increased temperature generally enhances solubility for many ionic compounds, making it essential to consider when studying this compound.
  • pH Levels: As an ammonium compound, its solubility may vary with pH, affecting protonation states and, subsequently, solubility behavior.

In general, one might expect N'-[1-[4-[[amino-[[amino(azaniumyl)methylene]amino]methylene]amino]phenyl]ethylideneamino]carbamimidoyl]ammonium;dichloride to be soluble in aqueous environments, especially under conditions where ionic interactions can occur efficiently. Therefore, the conditions under which solubility is tested should replicate practical applications to understand its behavior thoroughly.

Interesting facts

Interesting Facts about N'-[1-[4-[[amino-[[amino(azaniumyl)methylene]amino]methylene]amino]phenyl]ethylideneamino]carbamimidoyl]ammonium;dichloride

This complex compound is a fascinating example of modern organic chemistry, demonstrating the intricate designs that can be achieved with amine functionalities. Here are some intriguing aspects of this chemical:

  • Multi-Functional Moieties: The structure features various amino groups that give it unique properties, allowing it to act as a building block in complex organic reactions.
  • Biological Relevance: Compounds that contain amino groups are often integral in biological systems. This compound may exhibit potential applications in medicinal chemistry, as it could mimic biological interactions.
  • Potential Catalytic Properties: Given its nitrogen-rich framework, it might participate in catalytic processes, aiding in the synthesis of other complex molecules.
  • Understanding the Structure: The name of the compound indicates a highly intricate structure, which can present exciting challenges and opportunities for chemists focused on synthesis and characterization.

As a chemist, one might ponder the potential applications of such compounds in designing pharmaceuticals, where key interactions with biological macromolecules are required. Synthetic pathways that incorporate such intricate structures could lead to novel therapeutic agents. Furthermore, analyzing this compound can deepen our understanding of chemical bonding, reactivity, and the stabilization of large organic structures.

In summary, N'-[1-[4-[[amino-[[amino(azaniumyl)methylene]amino]methylene]amino]phenyl]ethylideneamino]carbamimidoyl]ammonium;dichloride serves as an excellent example that underscores the importance of exploring the vast chemical landscape and the potential for discovery in the realm of organic synthesis.