Chemistry:TTFB (chemical)

From HandWiki
TTFB
TTFB structure.svg
Identifiers
3D model (JSmol)
ChEBI
ChEMBL
ChemSpider
KEGG
Properties
C8HCl4F3N2
Molar mass 323.91 g·mol−1
Hazards
Lethal dose or concentration (LD, LC):
23 mg/kg (mice, intraperitoneal)[1]
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references

TTFB (4,5,6,7-Tetrachloro-2-trifluoromethylbenzimidazole) is a halogenated benzimidazole derivative that acts as an uncoupling agent.[2]

See also

References

  1. Ilivicky, J; Casida, JE (June 1969). "Uncoupling action of 2,4-dinitrophenols, 2-trifluoromethylbenzimidazoles and certain other pesticide chemicals upon mitochondria from different sources and its relation to toxicity.". Biochemical Pharmacology 18 (6): 1389–401. doi:10.1016/0006-2952(69)90252-4. PMID 5799112. 
  2. Beechey, RB (January 1966). "The uncoupling of respiratory-chain phosphorylation by 4,5,6,7-tetrachloro-2-trifluoromethylbenzimidazole.". The Biochemical Journal 98 (1): 284–9. doi:10.1042/bj0980284. PMID 4223043.