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2-Ethylguanidine

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Identification
Molecular formula
C3H10N3
CAS number
5457-81-6
IUPAC name
2-ethylguanidine
State
State
2-Ethylguanidine is typically in a liquid state at room temperature.
Melting point (Celsius)
-41.00
Melting point (Kelvin)
232.15
Boiling point (Celsius)
173.00
Boiling point (Kelvin)
446.15
General information
Molecular weight
101.16g/mol
Molar mass
101.1590g/mol
Density
0.9000g/cm3
Appearence

2-Ethylguanidine typically appears as a clear, colorless liquid.

Comment on solubility

Solubility of 2-ethylguanidine

2-ethylguanidine is an intriguing compound with notable solubility characteristics that merit our attention. This organic base demonstrates solubility in various solvents, primarily due to its polar nature and the presence of functional groups that can interact favorably with solvent molecules.

Key points regarding its solubility include:

  • Water Solubility: 2-ethylguanidine is highly soluble in water. Its ability to form hydrogen bonds with water molecules enhances its dissolution.
  • Alcohol Solubility: It also exhibits good solubility in alcohols, particularly in methanol and ethanol. This property is significant for its application in various chemical reactions and formulations.
  • Organic Solvents: While it is less soluble in non-polar solvents, it can still dissolve to some extent, which may limit its applications in those environments.

Overall, the solubility of 2-ethylguanidine is primarily influenced by factors such as temperature, pH levels, and the presence of other solutes. As quaternary ammonium compounds can also affect solubility dynamics, understanding these interactions can provide insights into its behavior in different chemical contexts. In practical applications, the solubility of this compound plays a critical role in its usability for synthesis and biological interactions.

Interesting facts

Interesting Facts About 2-Ethylguanidine

2-Ethylguanidine is a fascinating organic compound that belongs to the guanidine family, known for its basic properties and biological significance. Here are some intriguing aspects:

  • Biological Relevance: The compound plays a notable role in biochemistry and pharmacology. It is involved in numerous biological processes and is considered a metabolite in various organisms.
  • Structure and Function: With its guanidine structure, 2-ethylguanidine exhibits strong basicity, contributing to its reactivity and interactions with other molecules. This makes it useful in both organic synthesis and as a reactive agent in several chemical reactions.
  • Potential Applications: Due to its unique properties, 2-ethylguanidine has potential applications in the development of pharmaceuticals, such as anti-inflammatory agents and other therapeutic compounds.
  • Research Interest: Scientists are increasingly interested in 2-ethylguanidine due to its intriguing interactions. For example, much research is focused on understanding how this compound can impact metabolic pathways or influence enzymatic activities.
  • Environmental Impact: Like many organic compounds, understanding the environmental fate of 2-ethylguanidine is crucial. Thorough studies help assess the potential health and ecological risks associated with its release into the environment.

Overall, 2-ethylguanidine is a compound that demonstrates the intricate relationship between structure and function in chemistry. Its diverse applications and biological relevance make it an interesting subject for ongoing research and exploration.

Synonyms
N-Ethylguanidine
503-69-5
DTXSID10198306
DTXCID00120797
RefChem:163349
1-ethylguanidine
2-ethylguanidine
Guanidine, ethyl-
EGD
guanidinoethane
4-ethyl guanidine
SCHEMBL181519
SCHEMBL350123
SCHEMBL350124
SCHEMBL677877
SCHEMBL689417
SCHEMBL6439109
SCHEMBL10772109
SCHEMBL10772112
SCHEMBL17022788
AKOS009157080
DB-071182
EN300-317747
Q27459943