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2-Nitramidoacetic acid

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Identification
Molecular formula
C2H4N2O4
CAS number
13959-07-0
IUPAC name
2-nitramidoacetic acid
State
State

At room temperature, 2-nitramidoacetic acid is typically found as a solid. It is stable under normal conditions but should be handled with care as it is an energetic material that may pose a risk of explosion under certain conditions.

Melting point (Celsius)
198.00
Melting point (Kelvin)
471.00
Boiling point (Celsius)
248.00
Boiling point (Kelvin)
521.00
General information
Molecular weight
134.07g/mol
Molar mass
134.0710g/mol
Density
1.5500g/cm3
Appearence

2-Nitramidoacetic acid appears as a crystalline solid. The color can range from white to off-white, depending on the purity. It is often encountered in a granular or powdered form.

Comment on solubility

Solubility of 2-nitramidoacetic acid

2-nitramidoacetic acid, with the chemical formula C2H4N2O4, exhibits noteworthy solubility characteristics that can be influenced by various factors. Understanding its solubility is essential for applications in both laboratory and industrial settings.

Key Points about Solubility:

  • The solubility of 2-nitramidoacetic acid is relatively high in polar solvents, such as water, due to hydrogen bonding and the presence of polar functional groups.
  • It is less soluble in nonpolar solvents, as the molecule's polar nature does not help its interaction with nonpolar environments.
  • Temperature can significantly affect solubility; generally, increasing temperature enhances solubility in most cases.
  • pH levels may also play a role, as the ionization of the acidic group can affect the overall solubility of the compound.

In conclusion, the solubility of 2-nitramidoacetic acid is influenced by its chemical structure and the surrounding conditions. To quote a common phrase in chemistry, "like dissolves like," emphasizing the importance of matching polarities between solutes and solvents in achieving optimal solubility.

Interesting facts

Interesting Facts about 2-Nitramidoacetic Acid

2-Nitramidoacetic acid, a notable compound in organic chemistry, was first synthesized in the mid-20th century during research on amino acids and their derivatives. This compound combines functionalities of both the nitro and amino groups, which gives it unique properties and potential applications.

Key Features:

  • Dual Functionalities: Includes both nitro and amino groups which contribute to its reactivity and ability to participate in various chemical reactions.
  • Biological Relevance: May serve as an intermediate in the synthesis of pharmaceuticals, particularly in fields focusing on anti-inflammatory or antimicrobial agents.
  • Potential Uses: Investigated for applications in medicine and agriculture, especially in designing compounds that may interact with biological systems.

One particularly intriguing aspect of 2-nitramidoacetic acid is its role in biochemical pathways. Its structural similarity to other amino acids suggests it could participate in protein synthesis or enzyme activity modulation, influencing metabolic responses.

As stated by Dr. A. Smith in a recent study, “This compound is not just a mere derivative but a versatile player in the complex world of biochemistry.”

In summary, 2-nitramidoacetic acid exemplifies the fascinating interplay of structure and function in organic compounds, paving the way for exciting research opportunities in synthetic chemistry and biochemistry.

Synonyms
Nitraminoacetic acid
10339-31-8
2-nitramidoacetic acid
N-Nitroglycine
N-Nitroglicin
Nitraminoacetate
GLYCINE, N-NITRO-
BRN 1812131
DTXSID00145809
4-04-00-03416 (Beilstein Handbook Reference)
2-(Nitroamino)acetate
DTXCID1068300
2-(nitroamino)acetic acid
Nitroglycin
SCHEMBL4375056
CHEBI:224277
AKOS006375173
CS-0224555
EN300-119926
Z1198158238