hot selling kenya chemical additives mbt 2-mercaptobenzothiazole
hot selling kenya chemical additives mbt 2-mercaptobenzothiazole
hot selling kenya chemical additives mbt 2-mercaptobenzothiazole
hot selling kenya chemical additives mbt 2-mercaptobenzothiazole
hot selling kenya chemical additives mbt 2-mercaptobenzothiazole
  • What is 2 mercaptobenzothiazole?
  • What is 2-Mercaptobenzothiazole? 2-Mercaptobenzothiazole (MBT) is an industrial chemical that is used principally in the manufacture of rubber. What were the results of the IARC Monographs evaluation of MBT?
  • What is 2-Mercaptobenzothiazole (MBT) vulcanization accelerator?
  • 2-Mercaptobenzothiazole (MBT) is one of the most important vulcanization accelerators in the industrial production of rubber, especially car tires. Given its wide use in household articles and industrial rubber products it has a high potential to migrate into the environment. Humans can be exposed by dermal, oral, or inhalative routes.
  • What is the standard state of 2-mercaptobenzothiazole?
  • Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). 2-Mercaptobenzothiazole is an organosulfur compound with the formula C6H4(NH)SC=S. A white solid, it is used in the sulfur vulcanization of rubber.
  • Are mercaptobenzothiazole derivatives cytotoxic?
  • 2-Mercaptobenzothiazole derivatives were also identified, showing interesting cytotoxic effects in cancer cell models. In these molecules, amide and sulfonimide groups were inserted, obtaining compounds targeting different targets, such as PPARα, CA IX, and tubulin.
  • What is mercaptobenzothiazole disulfide?
  • Oxidation gives mercaptobenzothiazole disulfide. This disulfide reacts with amines to give sulfenamide derivatives such 2-morpholinodithiobenzothiazole. These compounds are used in sulphur vulcanization, where they act as accelerators.
  • What happens if 2 mercaptobenzothiazole reacts with Z and E sulfoxides?
  • Reaction of Z and E isomeric sulfoxides with 2-mercaptobenzothiazole led to the splitting of thiazolidine ring in penicillin nucleus and to the formation of (E) and (Z)-alkylidene-4-heteroaryldithioazetidin-2-ones 5–6 and 7–11 (Fig. 4).