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5-methylphenazine-1,3-diamine

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Identification
Molecular formula
C13H13N3
CAS number
10435-20-4
IUPAC name
5-methylphenazin-5-ium-1,3-diamine
State
State

At room temperature, 5-methylphenazine-1,3-diamine is typically in a solid state. This compound is usually in a powdery or crystalline form, with its characteristic color and potential sheen making it identifiable in industrial and laboratory settings.

Melting point (Celsius)
230.00
Melting point (Kelvin)
503.15
Boiling point (Celsius)
370.00
Boiling point (Kelvin)
643.15
General information
Molecular weight
211.27g/mol
Molar mass
211.2710g/mol
Density
1.2000g/cm3
Appearence

5-Methylphenazine-1,3-diamine appears as a crystalline solid. The color of the crystals can vary depending on purity, but it is often found in brown or reddish-brown. Like many phenazine derivatives, it can exhibit a metallic or shimmering luster.

Comment on solubility

Solubility of 5-methylphenazin-5-ium-1,3-diamine

5-methylphenazin-5-ium-1,3-diamine is a fascinating compound with nuanced solubility characteristics that are worth exploring.

Its solubility profile can be evaluated through the following key points:

  • Polar vs. Non-Polar Solvent: The presence of the diamine functional group indicates that this compound may have polar characteristics, making it more soluble in polar solvents such as water or alcohols.
  • Temperature Influence: Like many organic compounds, its solubility may increase with temperature. Thus, heating a solvent could significantly enhance the dissolution of 5-methylphenazin-5-ium-1,3-diamine.
  • pH Sensitivity: As an ionic compound, its solubility might also be affected by the pH of the solution, highlighting the importance of testing in different pH environments.
  • Complex Formation: The compound may have the potential to form complexes with other ions, which can inadvertently enhance or inhibit its solubility.

In summary, exploring the solubility of 5-methylphenazin-5-ium-1,3-diamine reveals a complex interplay of polarity, temperature, pH, and interactions with other species. Understanding these factors is essential for effectively utilizing this compound in various chemical applications.

Interesting facts

Exploring 5-methylphenazin-5-ium-1,3-diamine

5-methylphenazin-5-ium-1,3-diamine is a fascinating compound, categorized under phenazines, which are nitrogen-containing heterocyclic compounds. Here are some compelling facts about this compound:

  • Historical Significance: Phenazines, including 5-methylphenazin-5-ium-1,3-diamine, were first discovered in the late 19th century. They have been extensively studied for their unique electronic properties.
  • Biological Activity: Research indicates that phenazine derivatives can exhibit various biological activities, including antimicrobial and antitumor properties. This opens up possibilities for applications in medicinal chemistry.
  • Role in Biology: Some phenazine compounds play a vital role in microbial metabolism. They are involved in electron transport processes, which are crucial for energy production in certain bacteria.
  • Color Evolution: Compounds like 5-methylphenazin-5-ium-1,3-diamine are known for their vibrant colors, making them valuable for use as dyes and pigments in various industries.
  • Complex Structure: The structure of this compound includes a quaternary nitrogen atom, which contributes to its stability and reactivity, making it a subject of interest in the field of synthetic organic chemistry.

In summary, 5-methylphenazin-5-ium-1,3-diamine is not just a chemical compound; it is a gateway to understanding the intricate connections between chemistry and biology. It highlights the significance of nitrogen-containing compounds in nature and their potential applications in various scientific fields.

Synonyms
DIAMINOMETHYLPHENAZINIUM CL
1,3-diamino-5-methylphenazin-5-ium
SCHEMBL19970683
DTXSID10862530