phone
Email
Online Inquiry
Verification code

Uric acid

Catalog Number
ACM69932-1
CAS
69-93-2
Structure
IUPAC Name
7,9-Dihydro-3H-purine-2,6,8-trione
Synonyms
2,6,8-Trioxopurine
Molecular Weight
168.11
Molecular Formula
C5H4N4O3
Canonical SMILES
C12=C(NC(=O)N1)NC(=O)NC2=O
InChI
InChI=1S/C5H4N4O3/c10-3-1-2(7-4(11)6-1)8-5(12)9-3/h(H4,6,7,8,9,10,11,12)
InChI Key
LEHOTFFKMJEONL-UHFFFAOYSA-N
Boiling Point
297.02 °C
Melting Point
>300 °C(lit.)
Flash Point
475.7 °C
Purity
95%
Density
1.9 g/cm³
Appearance
White to off-white crystalline
Storage
Sealed in dry, 2-8 °C
Active Content
95%
Physical State
Solid
Typical Applications
Use as antioxidant.
Spec Sheet
Case Study

Synthesis of Graphitic Carbon Nitride via the Reaction of Melamine and Urea

Synthesis of Graphitic Carbon Nitride via the Reaction of Melamine and Urea Dante, Roberto C., et al. Materials Chemistry and Physics 130.3 (2011): 1094-1102.

Graphitic carbon nitride was synthesized starting from melamine and uric acid. Uric acid was chosen because it thermally decomposes and condenses with melamine at temperatures between 400-600 °C. The reagents were mixed with alumina and then treated in a furnace under a nitrogen flow. Alumina facilitates the deposition of the graphitic carbon nitride layers on the exposed surfaces. This method can be compared to in situ chemical vapor deposition (CVD). The infrared (IR) spectra and X-ray diffraction (XRD) patterns are consistent with the formation of graphitic carbon nitride based on a heptazine block structure. Transmission electron microscopy (TEM) analysis showed that these carbon nitrides exhibit poor crystallinity and nanoscale texture. The thermal decomposition of graphitic carbon nitride occurs via cyano formation, involving bridging tertiary nitrogen and bonded carbon belonging to the heptazine ring, which leads to ring opening and subsequent network breakdown. This inference was made by correlating IR and X-ray photoelectron spectroscopy (XPS) results. This appears to be a simple and promising route for synthesizing graphitic carbon nitride. Our final material is a composite made of alumina cores covered with carbon nitride layers.

Synthesis of Uric Acid-Based Nano-Organocatalyst

Synthesis of Uric Acid-Based Nano-Organocatalyst Kalhor, Sima, et al. Molecular Catalysis 507 (2021): 111549.

In this study, a novel bio-based acidic nano-organocatalyst was designed, synthesized, and fully characterized through the condensation reaction of uric acid and phosphorous acid. The resulting compound, named Theanine Tetraphosphonic Acid (TTPA), was prepared under reflux in ethanol.
Experimental Procedure
In a 50 mL round-bottom flask, a mixture containing uric acid (1 mmol, 0.17 g), paraformaldehyde (4 mmol, 0.12 g), phosphorous acid (4 mmol, 0.32 g), p-TSA (10 mol%, 0.017 g), and 25 mL of ethanol was refluxed for 18 hours. Following this period, the resulting white precipitate was filtered off and dried under vacuum to yield Theanine Tetraphosphonic Acid (TTPA).

Custom Q&A

What is the molecular weight of uric acid?

The molecular weight of uric acid is 168.11.

What is the molecular formula of uric acid?

The molecular formula of uric acid is C5H4N4O3.

What is the physical state of uric acid?

Uric acid is in a solid physical state.

What are some synonyms for uric acid?

Some synonyms for uric acid include 1H-Purine-2,6,8(3H)-trione and 7,9-dihydro-.

What percentage of uric acid is active?

95% of uric acid is active.

What is the CAS number of uric acid?

The CAS number of uric acid is 69-93-2.

What is the typical application of uric acid?

Uric acid is used as an antioxidant.

How many carbon atoms are present in the molecular formula of uric acid?

There are 5 carbon atoms present in the molecular formula of uric acid.

What role does uric acid play in the body?

Uric acid is a waste product that is excreted through the kidneys and plays a role in antioxidant defense.

How does the molecular weight of uric acid compare to that of other molecules?

The molecular weight of uric acid is relatively small compared to many other molecules, at 168.11.

❈ Please kindly note that our products are for research use only.

PAGE TOP