| |||
Names | |||
---|---|---|---|
Preferred IUPAC name
2-Sulfanylidene-1,3-diazinane-4,6-dione | |||
Other names
2-Thioxodihydropyrimidine-4,6(1H,5H)-dione
2-Thiobarbituric acid | |||
Identifiers | |||
3D model (JSmol)
|
|||
ChEMBL | |||
ChemSpider | |||
ECHA InfoCard | 100.007.260 | ||
EC Number |
| ||
PubChem CID
|
|||
UNII | |||
CompTox Dashboard (EPA)
|
|||
| |||
| |||
Properties | |||
C4H4N2O2S | |||
Molar mass | 144.15 g/mol | ||
Melting point | 245 °C (473 °F; 518 K) | ||
-72.9·10−6 cm3/mol | |||
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
|
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]
It is also used in Kodak Fogging Developer FD-70, part of the Kodak Direct Positive Film Developing Outfit for making black and white slides (positives).[2]
References
- ^ Thiobarbituric acid reactive substances (TBARS) Assay Archived 2006-09-14 at the Wayback Machine, AMDCC Protocols, Animal Models of Diabetic Complications Consortium
- ^ "Kodak Direct Positive Film 5246" (PDF). 125px.com. Kodak. Retrieved 6 November 2019.