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Nipradilol

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Identification
Molecular formula
C17H26N4O3
CAS number
/78324-97-1
IUPAC name
2-nitro-1-nitroso-1-pentyl-guanidine
State
State

At room temperature, Nipradilol is typically in a solid state, existing as a powder.

Melting point (Celsius)
135.00
Melting point (Kelvin)
408.15
Boiling point (Celsius)
253.00
Boiling point (Kelvin)
526.15
General information
Molecular weight
369.41g/mol
Molar mass
369.4120g/mol
Density
1.4600g/cm3
Appearence

Nipradilol typically appears as a crystalline powder. It is often white or off-white in color.

Comment on solubility

Solubility of 2-nitro-1-nitroso-1-pentyl-guanidine

The solubility of 2-nitro-1-nitroso-1-pentyl-guanidine is quite intriguing and can be influenced by various factors. Understanding its solubility is crucial for its applications in different fields.

Key Points to Consider:

  • Polarity: The presence of nitro and nitroso groups may increase the polar nature of this compound, potentially enhancing its solubility in polar solvents such as water and methanol.
  • Solvent Characteristics: Typically, compounds with guanidine groups can exhibit better solubility in solvents that can engage in hydrogen bonding.
  • Temperature Effects: Solubility may also vary with temperature. An increase in temperature generally leads to greater solubility for many chemical compounds.
  • pH Influence: The solubility might change in different pH environments due to protonation forms that guanidine can undergo.

As with many organic compounds, “like dissolves like” is a rule of thumb. Therefore, understanding the molecular structure can give insights into which solvents will effectively dissolve 2-nitro-1-nitroso-1-pentyl-guanidine. Overall, detailed experimentation would be required to ascertain its solubility profile accurately.

Interesting facts

Interesting Facts about 2-Nitro-1-nitroso-1-pentyl-guanidine

2-Nitro-1-nitroso-1-pentyl-guanidine is a fascinating compound that garners attention in both academic and industrial settings. Here are some notable points about this intriguing chemical:

  • Dual functionality: The presence of both nitro and nitroso groups in the structure makes this compound unique and allows researchers to explore its reactivity and potential applications in various fields.
  • Roles in synthesis: Compounds like 2-nitro-1-nitroso-1-pentyl-guanidine often serve as intermediates in the synthesis of more complex nitrogenous organic molecules, showcasing the versatility of guanidine derivatives.
  • Biological implications: There is interest in the biological activity of guanidine derivatives, including their role in pharmacology and potential use as therapeutic agents. The nitro and nitroso groups can play significant roles in interactions with biological targets.
  • Environmental consideration: As with many nitro compounds, there is a focus on the environmental impact and degradation pathways, making studies of this compound relevant for understanding pollution and sustainability.
  • Insight into chemical behavior: The nitroso and nitro functionalities make this compound a subject of study for understanding mechanisms of chemical reactions and stability, providing valuable insights into nitrosation and nitration processes.

In summary, 2-nitro-1-nitroso-1-pentyl-guanidine presents a nexus of synthetic utility, biological interest, and environmental relevance, making it an exciting topic for both seasoned chemists and students alike.

Synonyms
13010-10-1
CID 25593