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Alloxanic acid

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Identification
Molecular formula
C3H4N2O4
CAS number
303-36-6
IUPAC name
2-oxo-2-ureido-acetic acid
State
State

The compound is a solid at room temperature, appearing as a white crystalline powder.

Melting point (Celsius)
148.00
Melting point (Kelvin)
421.15
Boiling point (Celsius)
255.00
Boiling point (Kelvin)
528.15
General information
Molecular weight
146.10g/mol
Molar mass
146.0980g/mol
Density
2.1300g/cm3
Appearence

Alloxanic acid typically appears as a white crystalline solid. It is not commonly encountered outside of specific scientific applications.

Comment on solubility

Solubility of 2-oxo-2-ureido-acetic acid (C3H4N2O4)

2-oxo-2-ureido-acetic acid, also known as a derivative of uracil, exhibits notable solubility characteristics in various solvents. Understanding its solubility is crucial for applications in biochemical research and synthesis.

Solubility Characteristics:

  • Polar Solvents: This compound is highly soluble in water due to its polar functional groups, enhancing its interactions with water molecules.
  • Non-Polar Solvents: In non-polar solvents such as hexane, 2-oxo-2-ureido-acetic acid demonstrates very limited solubility, which can be attributed to its polar nature.
  • pH Effects: The solubility can also be influenced by the pH of the solution. Under acidic conditions, the compound may exist in protonated forms, potentially affecting its overall solubility.
  • Temperature Dependency: As with many organic compounds, an increase in temperature generally enhances solubility, allowing more of the compound to dissolve in a given solvent.

To summarize, 2-oxo-2-ureido-acetic acid is primarily soluble in water and other polar solvents while exhibiting minimal solubility in non-polar environments. This solubility behavior is pivotal for its utilization in various chemical and biological applications, making it a valuable compound in the field of chemistry.

Interesting facts

Interesting Facts About 2-Oxo-2-ureido-acetic Acid

2-Oxo-2-ureido-acetic acid, also known as an important intermediate in the synthesis of various bioactive compounds, displays a fascinating array of properties and applications. Here are some key points to consider:

  • Biochemical Relevance: This compound is pivotal in metabolic pathways, particularly in the synthesis of amino acids and as a precursor to other significant nitrogen-containing compounds.
  • Potential Therapeutic Uses: Researchers are exploring its potential in pharmaceuticals, especially for developing drugs targeting metabolic disorders.
  • Amino Acid Derivative: As a derivative of amino acids, it opens doors to the understanding of protein synthesis and the role of nitrogen in biological systems.
  • Research Applications: It is often utilized in biochemical assays and research to study enzymatic reactions involving amino acid metabolism.
  • Synthetic Utility: Chemists find this compound valuable for creating diverse chemical entities by modifying its functional groups, leading to novel compounds with desirable properties.

Understanding 2-oxo-2-ureido-acetic acid not only enriches our knowledge of organic chemistry but also highlights the intricacies of metabolic processes in living organisms. As the scientific community continues to explore its applications, this compound serves as a reminder of the profound connections between chemistry and life.

Synonyms
Oxaluric acid
585-05-7
3-Oxaluric acid
oxalureate
Monooxalylurea
2-(carbamoylamino)-2-oxoacetic acid
ureido(oxo)acetic acid
Acetic acid, [(aminocarbonyl)amino]oxo-
Acetic acid, ((aminocarbonyl)amino)oxo-
Carbamoyloxamic acid
Carbamoyloxalamidsaeure
onooxalylurea
Oxalursaure
2-oxo-2-ureidoacetic acid
carbamoylamino(oxo)acetic acid
SCHEMBL899896
(carbamoylamino)(oxo)acetic acid
CHEBI:16582
DTXSID00207214
UWBHMRBRLOJJAA-UHFFFAOYSA-N
AKOS006273229
[(Aminocarbonyl)amino](oxo)acetic acid #
C00802
Q27101984
UGC