| |||
Names | |||
---|---|---|---|
Preferred IUPAC name
5,5-Dihydroxypyrimidine-2,4,6(1H,3H,5H)-trione | |||
Other names
5,5-Dihydroxybarbituric acid
| |||
Identifiers | |||
3D model (JSmol)
|
|||
ChEBI | |||
ChEMBL | |||
ChemSpider | |||
ECHA InfoCard | 100.000.057 | ||
EC Number |
| ||
MeSH | Alloxan | ||
PubChem CID
|
|||
UNII |
| ||
CompTox Dashboard (EPA)
|
|||
| |||
| |||
Properties | |||
C4H4N2O5 | |||
Molar mass | 160.07 g/mol | ||
Appearance | pale yellow solid | ||
Density | 1.639 g/cm3 (anhydrous) | ||
Melting point | 254 °C (489 °F; 527 K) (decomposition) | ||
0.29 g/100 mL[2] | |||
Hazards | |||
Safety data sheet (SDS) | MSDS | ||
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
|
Alloxan, sometimes referred to as alloxan hydrate, is an organic compound with the formula OC(N(H)CO)2C(OH)2. It is classified as a derivative of pyrimidine. The anhydrous derivative OC(N(H)CO)2CO is also known, as well as a dimeric derivative. These are some of the earliest known organic compounds. They exhibit a variety of biological activities.
OS
was invoked but never defined (see the help page).