industrial grade jordan mbt (m) 2-mercaptobenzothiazole
industrial grade jordan mbt (m) 2-mercaptobenzothiazole
industrial grade jordan mbt (m) 2-mercaptobenzothiazole
industrial grade jordan mbt (m) 2-mercaptobenzothiazole
industrial grade jordan mbt (m) 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 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 2-mercaptobenzothiazole used for?
  • ChEBI: 2-Mercaptobenzothiazole is a 1,3-Benzothiazole substituted at the 2-position with a sulfanyl group. It is used as a vulcanisation accelerator in the crosslinking of rubber. The Journal of Organic Chemistry, 26, p. 3436, 1961 DOI: 10.1021/jo01067a101 Pale yellow to tan crystalline powder with a disagreeable odor. Insoluble in water.
  • 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.
  • How is 2-mercaptobenzothiazole produced?
  • 2-Mercaptobenzothiazole is produced by reacting aniline, carbon disulfide, and sulfur at high temperature and pressure; the product is then purified by dissolution in a base to remove the dissolved organics. Re-precipitation is achieved by the addition of acid (Kirk-Othmer, 1982; NTP, 1988).