Substance
ID:362938
Names and Identifiers
IUPAC Traditional name
allantoin
Synonyms
Glyoxylic(acid) diureide5-Ureidohydantoin5-脲尿囊素尿囊素Allantoin尿基间二-氮茂烷-2,4-二酮NSC 7606
IUPAC name
(2,5-dioxoimidazolidin-4-yl)urea
Registration numbers
CAS Number
EC Number
Beilstein Number
MDL Number
PubChem SID
Properties
Product Information
Empirical Formula (Hill Notation)
C4H6N4O3
Ignition Residue
≤0.2%
Purity
≥98.0% (N)
Safety Information
GHS Signal Word
Warning
German water hazard class
1
RTECS
YT1600000
MSDS Link
European Hazard Symbols
Harmful (Xn)Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
GHS Hazard statements
H302
Risk Statements
22
GHS Pictograms
Acute toxicity (oral, dermal, inhalation), category 4
Skin irritation, category 2
Eye irritation, category 2
Skin sensitisation, category 1
Specific Target Organ Toxicity – Single exposure, category 3
Safety Statements
22
Physical Property
Melting Point
230 °C (dec.)(lit.)
Molecule Details
Biochem/physiol Actions
Purine metabolite via the uric acid pathway. Uric acid also reacts with free radicals to produce allantoin, thus allantoin may be a useful biomarker for oxidative stress.
Application
Reactant for: Synthesis of Mannich bases for use as antibacterial agents1 Synthesis of sulofenur analogs for use as antitumor agents2
Purine metabolite via the uric acid pathway. Uric acid also reacts with free radicals to produce allantoin, thus allantoin may be a useful biomarker for oxidative stress.
Application
Reactant for: Synthesis of Mannich bases for use as antibacterial agents1 Synthesis of sulofenur analogs for use as antitumor agents2
Molecular Spectra
No Data Available
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References
No Data Available
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