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2,2-diureidoacetic acid

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Identification
Molecular formula
C3H8N4O3
CAS number
21160-04-9
IUPAC name
2,2-diureidoacetic acid
State
State

2,2-Diureidoacetic acid is a solid at room temperature. It is stable and does not readily sublime or decompose under standard conditions of temperature and pressure.

Melting point (Celsius)
215.00
Melting point (Kelvin)
488.00
Boiling point (Celsius)
250.00
Boiling point (Kelvin)
523.00
General information
Molecular weight
175.12g/mol
Molar mass
175.0980g/mol
Density
1.4600g/cm3
Appearence

2,2-Diureidoacetic acid typically appears as a white crystalline powder. It is relatively soluble in water and has a crystalline structure typical of many organic compounds containing multiple nitrogen moieties.

Comment on solubility

Solubility of 2,2-Diureidoacetic Acid (C3H8N4O3)

2,2-Diureidoacetic acid is known for its intriguing solubility characteristics, which can be summarized in the following points:

  • Polarity: The compound contains multiple polar functional groups, such as amides and carboxylic acids, which enhance its ability to interact with water.
  • Hydrogen Bonding: The presence of both NH and COOH groups allows for extensive hydrogen bonding with water molecules, increasing its solubility.
  • Aqueous Solubility: 2,2-Diureidoacetic acid is generally soluble in polar solvents like water, attributed to its ionic and polar nature.
  • Influence of pH: Solubility may vary with pH levels due to the dissociation of protons from the carboxylic acid group, enhancing its solubility in basic conditions.

In summary, the solubility of 2,2-diureidoacetic acid can be described as quite favorable in polar solvents, allowing for potential applications in various chemical reactions and biological systems. As noted, understanding the solubility behavior is crucial for utilizing this compound effectively in different scenarios.

Interesting facts

Interesting Facts about 2,2-Diureidoacetic Acid

2,2-Diureidoacetic acid is a fascinating compound that highlights the interplay between organic chemistry and biological applications. Here are some noteworthy aspects:

  • Biochemical Significance: This compound is of particular interest in biochemical research due to its structural similarities to amino acids. Such structural features help scientists understand protein synthesis and enzyme functions.
  • Synthesis: The synthesis of 2,2-diureidoacetic acid can be achieved through various methods, including the condensation of urea with glycine derivatives. This process exemplifies key reactions in organic synthesis, aiding in the formation of crucial bioactive compounds.
  • Pharmaceutical Applications: Compounds like this one often serve as precursors or intermediates in the production of pharmaceuticals. Their ability to interact with biological systems makes them valuable in drug discovery and development.
  • Functional Groups: The presence of multiple urea functional groups in its structure allows for significant hydrogen bonding, leading to interesting solubility and reactivity patterns that are explored in various chemical environments.
  • Researching the Unknown: The study of 2,2-diureidoacetic acid opens doors to research in areas like neurobiology, where it can be studied for potential neuroprotective effects due to its relationships with cellular functions.

Overall, 2,2-diureidoacetic acid serves as a bridge linking organic chemistry and pharmaceuticals, exemplifying how even simple organic compounds can have profound implications in science. Its unique structure and properties continue to intrigue researchers, prompting ongoing studies to explore its full potential.

Synonyms
Allantoic acid
99-16-1
Diureidoacetic acid
Acetic acid, bis[(aminocarbonyl)amino]-
2,2-bis(carbamoylamino)acetic acid
Allantoicacid
2,2-diureidoacetic acid
02WGT7SHWJ
Diureidoacetic acid
Bis((aminocarbonyl)amino)acetic acid
Bis[(aminocarbonyl)amino]acetic acid
EINECS 202-735-4
UNII-02WGT7SHWJ
102185-22-8
bis(carbamoylamino)acetic acid
DTXSID3059187
CHEBI:30837
acetic acid, bis((aminocarbonyl)amino)-
Diureido-acetic acid
Oprea1_555230
SCHEMBL483061
DTXCID8049096
CS-D1349
HY-B1514
CCG-51209
MFCD00007949
AKOS015837554
Acetic acid, bis((aminocarbonyl)amino)
Bis[(aminocarbonyl)amino]acetic acid #
FA16219
BS-33442
Acetic acid, 2,2bis((aminocarbonyl)amino)
DB-007241
NS00041382
Acetic acid, 2,2-bis((aminocarbonyl)amino)-
C00499
D86397
Q1067123
SR-01000640521-1