Thiobarbituric acid
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Names | |||
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Preferred IUPAC name 2-Sulfanylidene-1,3-diazinane-4,6-dione | |||
Other names 2-Thioxodihydropyrimidine-4,6(1H,5H)-dione 2-Thiobarbituric acid | |||
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3D model (JSmol) |
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ChEMBL |
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ChemSpider |
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ECHA InfoCard | 100.007.260 | ||
EC Number |
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CompTox Dashboard (EPA) |
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InChI
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Properties | |||
Chemical formula | C4H4N2O2S | ||
Molar mass | 144.15 g/mol | ||
Melting point | 245 °C (473 °F; 518 K) | ||
Magnetic susceptibility (χ) | -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). N verify (what is YN ?) Infobox references |
Chemical compound
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.
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