Informação sobre produto
- 1,3,4-Thiadiazolidine-2,5-dithione, 3-phenyl-, potassium salt
- 1,3,4-Thiadiazolidine-2,5-dithione, 3-phenyl-, potassium salt (1:1)
- 2-Mercapto-4-phenyl-1,3,4-thiadiazoline-5-thione potassium salt
- 3-Phenyl-5-mercapto-1,3,4-thiadiazole-2-thione
- 5-Mercapto-3-phenyl-1,3,4-thiadiazole-2-thione potassium salt
- 5-Mercapto-3-phenyl-1,3,4-thiadiazoline-2-thione potassium salt
- 5-Mercapto-3-phenyl-Δ<sup>4</sup>-1,3,4-thiadiazoline-2-thione potassium salt
- Ai3-62186
- Bismuthone
- Potassium 2-mercapto-4-phenyl-1,3,4-thiadiazoline-5-thione
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- Potassium 4-Phenyl-5-Thioxo-4,5-Dihydro-1,3,4-Thiadiazole-2-Thiolate
- Potassium 5-mercapto-3-phenyl-1,3,4-thiadiazole-2-thione
- Δ<sup>2</sup>-1,3,4-Thiadiazoline-5-thione, 2-mercapto-4-phenyl-, potassium deriv.
- Δ<sup>2</sup>-1,3,4-Thiadiazoline-5-thione, 2-mercapto-4-phenyl-, potassium salt
- Δ2-1,3,4-Thiadiazoline-5-thione, 2-mercapto-4-phenyl-, potassium salt
- 5-Mercapto-3-phenyl-Δ4-1,3,4-thiadiazoline-2-thione potassium salt
- Δ2-1,3,4-Thiadiazoline-5-thione, 2-mercapto-4-phenyl-, potassium deriv.
Bismuthiol II is a reagent that is used in the reaction mechanism of particle. It reacts with hydrochloric acid to form silver chloride, which can be detected by fluorescence probe. Bismuthiol II is also used as a plasma mass spectrometry (PMS) reagent, where it reacts with tellurium to form copper tellurate and bismuth tellurate. Bismuthiol II has been shown to have anti-cancer effects on cancer tissue during the extractant process. The extractant process utilizes a multi-walled carbon nanotube (MWCNT) to extract copper complexes from the tissue. This extraction process has been shown to enhance the analytical chemistry of bismuthiol II.
Propriedades químicas
Consulta técnica sobre: 3D-GAA33651 Bismuthiol II
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