Skip to main content

Amyl Nitrite

ADVERTISEMENT
Identification
Molecular formula
C5H11NO2
CAS number
110-46-3
IUPAC name
N-[3-aminopropyl(isopropyl)amino]-N-hydroxy-nitrous amide
State
State

In its pure form at room temperature, amyl nitrite is a liquid that readily evaporates due to its volatility. It is sensitive to light and air, which may cause it to discolor.

Melting point (Celsius)
-108.00
Melting point (Kelvin)
165.15
Boiling point (Celsius)
97.00
Boiling point (Kelvin)
370.15
General information
Molecular weight
101.15g/mol
Molar mass
101.1490g/mol
Density
0.9150g/cm3
Appearence

Amyl nitrite is a clear, yellowish liquid with a distinctive, fruity odor. It is volatile and flammable and is frequently used as a reagent in chemical and pharmaceutical applications.

Comment on solubility

Solubility of N-[3-aminopropyl(isopropyl)amino]-N-hydroxy-nitrous amide (C5H11NO2)

N-[3-aminopropyl(isopropyl)amino]-N-hydroxy-nitrous amide is a compound that exhibits unique solubility characteristics due to its structural features. Understanding its solubility can be crucial for its applications in various fields.

Factors Influencing Solubility

The solubility of this compound can be influenced by several factors, including:

  • Polarity: The presence of amino and hydroxyl functional groups enhances polarity, suggesting potential for dissolving in polar solvents.
  • Hydrogen Bonding: Ability to form hydrogen bonds can increase solubility in water and alcohols.
  • Temperature: Solubility may increase with temperature, as is typically the case for many organic compounds.

General Solubility Trends

Generally, compounds with the following characteristics tend to dissolve better:

  • Higher Molecular Weight: Larger molecules may exhibit lower solubility due to increased intermolecular attractions.
  • Functional Groups: More functional groups capable of hydrogen bonding typically result in increased solubility in polar solvents.

While specific solubility data for N-[3-aminopropyl(isopropyl)amino]-N-hydroxy-nitrous amide is not widely documented, it is reasonable to hypothesize that it demonstrates >em>moderate solubility in aqueous environments, particularly due to its hydrophilic functional groups. The exact solubility would need empirical testing under varied conditions to establish precise values.

In summary, the solubility of N-[3-aminopropyl(isopropyl)amino]-N-hydroxy-nitrous amide is expected to exhibit a combination of characteristics based on its molecular structure, with the potential for significant solubility in polar solvents.

Interesting facts

Interesting Facts about N-[3-aminopropyl(isopropyl)amino]-N-hydroxy-nitrous amide

N-[3-aminopropyl(isopropyl)amino]-N-hydroxy-nitrous amide is a fascinating compound that showcases the complexity and versatility of nitrogen-containing organic molecules. Here are some intriguing aspects of this compound:

  • Amine Chemistry: The presence of multiple amino groups in its structure highlights its role in amine chemistry, which is critical for biological processes and pharmaceuticals.
  • Hydroxyl Group Impact: The compound features a hydroxy group, which significantly enhances its reactivity and solubility in various environments, making it an important consideration in its applications.
  • Potential Applications: Compounds like this one often have potential uses in medicinal chemistry, particularly in drug design for conditions that require modulation of nitric oxide pathways.
  • Synthesis Challenges: The synthesis of nitrogen-rich compounds can pose challenges due to their stability and reactivity, making this compound a notable subject for synthetic chemists.
  • Biological Relevance: Compounds that interact with nitric oxide (NO) are crucial in pharmacology, especially in cardiovascular research and neurobiology.

Overall, N-[3-aminopropyl(isopropyl)amino]-N-hydroxy-nitrous amide exemplifies the rich tapestry of organic chemistry, where even minor modifications to molecular structure can lead to substantial differences in chemical properties and biological activities. Its study not only deepens our understanding of organic compounds but also paves the way for advancements in therapeutic applications.