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1,1,2-triphenylguanidine

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Identification
Molecular formula
C19H17N3
CAS number
102-06-7
IUPAC name
1,1,2-triphenylguanidine
State
State

At room temperature, 1,1,2-triphenylguanidine is a solid. It is often encountered in its crystalline form.

Melting point (Celsius)
148.00
Melting point (Kelvin)
421.15
Boiling point (Celsius)
623.00
Boiling point (Kelvin)
896.15
General information
Molecular weight
335.44g/mol
Molar mass
335.4380g/mol
Density
1.2140g/cm3
Appearence

1,1,2-Triphenylguanidine is a white to slightly yellow crystalline solid. It is typically odorless and stable under normal conditions. The compound may form larger crystals under specific conditions, displaying a glossy or translucent appearance.

Comment on solubility

Solubility of 1,1,2-Triphenylguanidine

1,1,2-Triphenylguanidine, a compound featuring an intriguing chemical structure, exhibits notable characteristics regarding its solubility. When exploring its solubility properties, a few key points stand out:

  • Nonpolar Solvent Compatibility: This compound is generally more soluble in nonpolar solvents such as toluene, which is attributed to the presence of multiple phenyl groups that enhance hydrophobic interactions.
  • Limited Solubility in Water: 1,1,2-Triphenylguanidine has a low solubility in water due to its hydrophobic nature. The presence of bulky phenyl groups prevents it from effectively interacting with water molecules.
  • Temperature Dependence: Solubility can be affected by temperature, as many organic compounds tend to increase their solubility in warmer conditions.

To sum up, while 1,1,2-triphenylguanidine may not dissolve readily in polar solvents like water, it finds better solvation in organic solvents, emphasizing the importance of considering solvent choice in chemical processes involving this compound. As a general observation, "solubility reflects the balance of forces in play," making it a crucial factor to evaluate in various applications.

Interesting facts

Interesting Facts about 1,1,2-Triphenylguanidine

1,1,2-Triphenylguanidine is a fascinating compound that showcases not just remarkable chemical properties but also significant applications in various fields. Here are some intriguing aspects of this compound:

  • Versatile Applications: 1,1,2-Triphenylguanidine is widely recognized in the realm of polymer science. It acts as a vulcanization accelerator, enhancing the process of rubber formation and improving the mechanical properties of rubber products.
  • Catalytic Behavior: The compound exhibits interesting catalytic properties, making it useful in various chemical reactions. It can facilitate polymerization and other transformations, which are critical in both industrial and laboratory settings.
  • Toxicity Considerations: Despite its utility, safety is paramount. It is essential to handle 1,1,2-triphenylguanidine with care due to its potential toxicity. Understanding the safety protocols is crucial for anyone working with this compound.
  • Research Significance: The compound serves as a subject of ongoing research, particularly in fields such as medicinal chemistry and material science. Its unique structure allows for modifications that can lead to the development of new materials with tailored properties.

In conclusion, the multifunctionality of 1,1,2-triphenylguanidine makes it a compound of interest not only for chemists but also for industries focused on innovation. As stated by renowned chemists, “Chemical compounds are the bedrock of progress in science, and the exploration of their potentials can lead to groundbreaking advancements.”


Synonyms
GUANIDINE, 1,1,3-TRIPHENYL-
603-53-2
1,1,3-Triphenylguanidine
N,N,N'-Triphenylguanidine
NSC 58954
BRN 2812062
9Y1R00K3F1
NSC-58954
UNII-9Y1R00K3F1
DTXSID40209055
4-12-00-00857 (Beilstein Handbook Reference)
GUANIDINE, N,N,N'-TRIPHENYL-
DTXCID60131546
Triphenyl guanidine
WLN: MUYMR&NR&R
MLS002693205
NSC58954
Guanidine,1,3-triphenyl-
NCIOpen2_002433
SCHEMBL109209
CHEMBL1702256
RYCFRVNAZOREPC-UHFFFAOYSA-N
HMS3094C21
SMR001559166