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DETA-NONOate

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Identification
Molecular formula
C4H13N5O3
CAS number
146724-94-9
IUPAC name
N-[bis(2-aminoethyl)amino]-N-oxido-nitrous amide
State
State

At room temperature, DETA-NONOate is usually found in a liquid state. It is an organic compound known for its application as a nitric oxide (NO) donor in biological and research studies. Proper handling and storage conditions are crucial to prevent degradation and ensure its effectiveness in various applications.

Melting point (Celsius)
78.50
Melting point (Kelvin)
351.60
Boiling point (Celsius)
251.80
Boiling point (Kelvin)
525.00
General information
Molecular weight
161.17g/mol
Molar mass
161.1690g/mol
Density
1.1600g/cm3
Appearence

DETA-NONOate typically appears as a colorless or pale yellow liquid. It is sensitive to light and moisture, which means it should be stored in a dark and dry environment to maintain its stability and efficacy.

Comment on solubility

Solubility of N-[bis(2-aminoethyl)amino]-N-oxido-nitrous amide

N-[bis(2-aminoethyl)amino]-N-oxido-nitrous amide, with the chemical formula C4H13N5O3, presents an intriguing case in terms of solubility characteristics. This compound, featuring multiple functional groups, is likely to exhibit varying solubility properties depending on the solvent used. Here are some key points regarding its solubility:

  • Polar solvents: Given its amine groups, the compound is expected to be quite soluble in polar solvents such as water and alcohols due to strong hydrogen bonding interactions.
  • Non-polar solvents: In contrast, this compound may show limited solubility in non-polar solvents, which can be attributed to the lack of significant non-polar regions in its molecular structure.
  • pH dependence: The solubility can also be influenced by the pH of the solution. In acidic conditions, protonation of the amine groups may enhance solubility, while basic conditions may lead to different solubility profiles.

In conclusion, the solubility of N-[bis(2-aminoethyl)amino]-N-oxido-nitrous amide is highly context-dependent, showcasing interesting behavior that makes it a compound of interest in solubility studies.

Interesting facts

Interesting Facts about N-[Bis(2-aminoethyl)amino]-N-oxido-nitrous amide

N-[Bis(2-aminoethyl)amino]-N-oxido-nitrous amide, commonly referred to in the scientific community for its unique properties, stands out due to its intricate molecular structure. Here are some captivating insights:

  • Dual Functionality: This compound exhibits both reducing and oxidizing characteristics, making it a versatile agent in various chemical reactions.
  • Biosynthesis Applications: The compound is known for its potential applications in biosynthesis, particularly due to its nitrogen-containing functional groups that can interact with biological systems.
  • Amine Moieties: The presence of two amine groups (2-aminoethyl) enhances its reactivity and compatibility with a variety of substrates, which is crucial for organic synthesis.
  • Pharmaceutical Relevance: Compounds of this class have garnered research interest for their potential therapeutic applications, including roles in drug design as intermediates or active pharmaceutical ingredients.
  • Environmental Impact: Understanding the behavior of such compounds in different environments is critical, as they can influence nitrogen cycles and may serve as indicators of pollution levels.

As the field of chemistry continually evolves, compounds like N-[bis(2-aminoethyl)amino]-N-oxido-nitrous amide not only broaden our understanding of chemical interactions but also pave the way for innovative solutions in various scientific disciplines. As one might say in the lab, “Every compound tells a story, and this one is just beginning!”