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About This Item
Empirical Formula (Hill Notation):
C3H2N2O3
CAS Number:
Molecular Weight:
114.06
PubChem Substance ID:
eCl@ss:
39161001
UNSPSC Code:
12352100
NACRES:
NA.22
EC Number:
204-434-3
MDL number:
Assay:
99%
Form:
powder
Product Name
Parabanic acid, 99%
InChI key
ZFLIKDUSUDBGCD-UHFFFAOYSA-N
InChI
1S/C3H2N2O3/c6-1-2(7)5-3(8)4-1/h(H2,4,5,6,7,8)
SMILES string
O=C1NC(=O)C(=O)N1
assay
99%
form
powder
mp
249 °C (dec.) (lit.)
Quality Level
Related Categories
Application
Reactant for:
Reactant for synthesis of:
- Enantiospecific assembly of homochiral, hexanuclear palladium complexes
- Mitsunobu reactions
- Quantitative cascade condensation reactions
Reactant for synthesis of:
- Pyridine derivatives
- Nitroesters
- Parabanic acid derivatives
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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H Kaur et al.
Chemico-biological interactions, 73(2-3), 235-247 (1990-01-01)
Uric acid is an end-product of purine metabolism in Man, and has been suggested to act as an antioxidant in vivo. Products of attack upon uric acid by various oxidants were measured by high performance liquid chromatography. Hypochlorous acid rapidly
L Hillered et al.
Neuroreport, 6(13), 1816-1820 (1995-09-11)
The authors used intracerebral microdialysis to harvest allantoin and parabanic acid, potential markers of in vivo oxygen radical activity, from the frontal lobe cortex of three patients in the neurointensive care unit after serious aneurysmal subarachnoid haemorrhage. Clinical events involving
X M He et al.
Acta crystallographica. Section B, Structural science, 44 ( Pt 3), 271-281 (1988-06-01)
The crystal structure of parabanic acid (1H,3H-imidazoletrione, C3H2N2O3, Mr = 114.1) at 123 K [monoclinic, P2(1)/n, Z = 4, a = 10.704 (2), b = 8.187 (2), c = 4.969 (1) A, beta = 92.32 (1)o] has been determined by
Reduction of oxalogenesis in a rapid gas chromatographic procedure for the analysis of oxalate ion in urine.
H A Moye et al.
Clinica chimica acta; international journal of clinical chemistry, 129(3), 385-390 (1983-04-25)
Suitability of reverse-phase columns from different sources for separation of uric acid from its oxidation products.
M Hicks et al.
Analytical biochemistry, 210(2), 428-430 (1993-05-01)
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