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Nitroguanidine

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Identification
Molecular formula
C1H4N4O3
CAS number
55-63-0
IUPAC name
2-[nitro(2,2,2-trinitroethyl)amino]acetic acid
State
State

This compound is generally found in a solid state at room temperature.

Melting point (Celsius)
119.00
Melting point (Kelvin)
392.15
Boiling point (Celsius)
255.00
Boiling point (Kelvin)
528.15
General information
Molecular weight
62.03g/mol
Molar mass
62.0280g/mol
Density
1.6800g/cm3
Appearence

Nitroguanidine typically appears as a white or colorless crystalline solid. The crystals can vary in size, appearing as a fine powder to small granules.

Comment on solubility

Solubility of 2-[nitro(2,2,2-trinitroethyl)amino]acetic acid

2-[nitro(2,2,2-trinitroethyl)amino]acetic acid, known for its complex structure, shows a specific solubility profile that is important for its applications. Here are some key points regarding its solubility:

  • Solvent Compatibility: This compound is generally soluble in polar solvents such as water and dimethyl sulfoxide (DMSO), allowing for various reactions and applications.
  • Temperature Effects: As with many organic compounds, increased temperature can enhance solubility in solvents, making it easier to dissolve.
  • pH Dependency: The solubility may vary with pH levels. Generally, its acidic functional groups can lead to improved solubility in basic conditions due to deprotonation.
  • Cautionary Note: Due to its nitro groups, it may exhibit unique stability issues in certain solvent systems, necessitating careful handling to avoid unwanted reactions.

Understanding the solubility of 2-[nitro(2,2,2-trinitroethyl)amino]acetic acid is vital for researchers and developers, as it directly influences how the compound can be utilized in various chemical applications.

Interesting facts

Interesting Facts about 2-[Nitro(2,2,2-trinitroethyl)amino]acetic Acid

2-[Nitro(2,2,2-trinitroethyl)amino]acetic acid is a fascinating compound with a variety of intriguing properties and applications. This compound, marked by its complex structure, is known for the following points of interest:

  • Unique Structure: The presence of both nitro groups and amino functionalities contributes to its interesting reactivity. Nitro groups often enhance the compound's electron-accepting characteristics.
  • Uses in Research: This compound is particularly significant in explosive chemistry. Its structural components are common in the field of propellant and explosive development.
  • Synergistic Effects: The combination of nitro and amino groups may lead to enhanced biological activity, making it a candidate for studies on various chemical interactions.
  • Environmental Impact: Understanding the degradation pathways of this compound is crucial, as nitro compounds can pose environmental challenges due to their persistence and potential toxicity.

As noted by a prominent chemist, "Exploring the realms of explosive chemistry not only broadens our understanding of chemical reactivity but also aids in the development of safer and greener alternatives." This highlights the importance of compounds like 2-[nitro(2,2,2-trinitroethyl)amino]acetic acid in both scientific research and environmental considerations.

Overall, the exploration of this compound opens numerous avenues for research and application in both academic and industrial settings.

Synonyms
BRN 2225758
GLYCINE, N-NITRO-N-(2,2,2-TRINITROETHYL)-
N-Nitro-N-(2,2,2-trinitroethyl)glycine
19836-29-4
DTXSID90173575
DTXCID5096066
RefChem:346577
N-(2,2,2-trinitroethyl)-N-nitroaminoacetic acid