Thiobarbituric acid
| |||
Names | |||
---|---|---|---|
IUPAC name
2-Thiobarbituric acid | |||
Other names
2-thioxodihydropyrimidine-4,6(1H,5H)-dione | |||
Identifiers | |||
504-17-6 | |||
3D model (Jmol) | Interactive image | ||
ChEMBL | ChEMBL584805 | ||
ChemSpider | 2005830 | ||
ECHA InfoCard | 100.007.260 | ||
EC Number | 207-985-8 | ||
PubChem | 2723628 | ||
| |||
| |||
Properties | |||
C4H4N2O2S | |||
Molar mass | 144.15 g/mol | ||
Melting point | 245 °C (473 °F; 518 K) | ||
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |||
verify (what is ?) | |||
Infobox references | |||
Thiobarbituric acid is an organic compound and a heterocycle. It is used as a reagent in assaying malondialdehyde (the TBARS assay of lipid peroxidation).[1]
References
- ↑ Thiobarbituric acid reactive substances (TBARS) Assay, AMDCC Protocols, Animal Models of Diabetic Complications Consortium
This article is issued from Wikipedia - version of the 3/21/2016. The text is available under the Creative Commons Attribution/Share Alike but additional terms may apply for the media files.