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Amidine

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Identification
Molecular formula
C13H28N6
CAS number
undefined
IUPAC name
2-[4-amino-5-[3-(3-aminopropylamino)propylamino]pentyl]guanidine
State
State
At room temperature, amidines like this typically exist as solid crystals with some hygroscopic properties, absorbing moisture from the air.
Melting point (Celsius)
102.00
Melting point (Kelvin)
375.15
Boiling point (Celsius)
204.00
Boiling point (Kelvin)
477.15
General information
Molecular weight
157.22g/mol
Molar mass
157.2240g/mol
Density
1.0900g/cm3
Appearence

Amidine compounds typically appear as solid substances. Their color and specific form can vary based on the particular amidine derivative, but they often appear as white to off-white crystalline powders.

Comment on solubility

Solubility of 2-[4-amino-5-[3-(3-aminopropylamino)propylamino]pentyl]guanidine

The solubility of the compound 2-[4-amino-5-[3-(3-aminopropylamino)propylamino]pentyl]guanidine, or C13H28N6, can be characterized with several interesting aspects:

  • Water Solubility: This compound is expected to have a good level of solubility in water, primarily due to the presence of multiple amino groups that can engage in hydrogen bonding with water molecules.
  • Solvents: In addition to water, the compound may dissolve well in polar organic solvents, which can stabilize the ionized ammonia groups present in the structure.
  • Ionization: The guanidine functional group in the structure contributes to its basicity, allowing it to become protonated in acidic environments, thus enhancing its solubility.
  • pH Impact: Variations in pH can substantially affect solubility; in neutral to basic pH environments, enhanced solubility due to ionization is expected.

In summary, the solubility characteristics of this compound can be attributed to its polar functional groups and its ability to interact favorably with various solvents, making it a compound of interest in many chemical applications.

Interesting facts

Interesting Facts about 2-[4-amino-5-[3-(3-aminopropylamino)propylamino]pentyl]guanidine

2-[4-amino-5-[3-(3-aminopropylamino)propylamino]pentyl]guanidine, often referred to simply as a complex guanidine derivative, is a fascinating compound in the field of chemistry and biochemistry. Here are some notable aspects:

  • Structure and Functionality: This compound features a unique structural framework that allows it to interact with various biological molecules. Its guanidine group is known for its ability to participate in hydrogen bonding, which is crucial for the compound’s biological activity.
  • Potential Applications: The compound has garnered interest in medical research and development due to its potential role in drug formulation. Researchers are exploring its application in therapeutics for conditions such as inflammation and cancer.
  • Research Insights: Various studies indicate that such guanidine derivatives can exhibit significant biological effects, including antimicrobial and antitumor properties. These properties make them valuable candidates for development as new pharmaceutical agents.
  • Biological Mechanisms: The presence of multiple amino groups within its structure contributes to its biological reactivity, as these groups can interact with receptor sites and enzymes in human physiology.
  • Synthesis Pathways: Chemists employ a range of synthetic methods to create this compound, with various approaches being explored to maximize yield and purity. This aspect of its synthesis showcases the creativity and innovation within organic chemistry.

Ultimately, 2-[4-amino-5-[3-(3-aminopropylamino)propylamino]pentyl]guanidine exemplifies the rich potential of small organic molecules in addressing complex biological challenges. Its intricate design not only reflects the beauty of chemical synthesis but also the importance of interdisciplinary approaches in modern scientific research.