General description Visit our Titration Center to learn more. concentration after dilution to 1L: 1/50mol/L (0.1N); amount of substance 1/50mol (3.161 g KMnO4) Packaging glass ampoule
General description Visit our Titration Center to learn more. concentration after dilution to 1L: 1/500mol/L (0.01N); amount of substance 1/500mol (0.3161 g KMnO4) Packaging glass ampoule
Application Suitable for heterogeneous oxidations. Other Notes Versatile oxidant in organic chemistry1; Oxidant for the decomposition by solubilization and fusion2,3
Application Suitable for heterogeneous oxidations. Layered MnO2 with very promising characteristics for battery applications is produced by thermal decomposition of KMnO4.1 Packaging 2.5 kg in poly bottle 25, 500 g in poly bottle
Application Layered MnO2 with very promising characteristics for battery applications is produced by thermal decomposition of KMnO4.1 Suitable for heterogeneous oxidations. Packaging 100, 500 g in poly bottle
Application Suitable for heterogeneous oxidations. Layered MnO2 with very promising characteristics for battery applications is produced by thermal decomposition of KMnO4.1 Packaging 2.5 kg in poly bottle 25, 500 g in poly bottle 2.5kg packaged in clear glass bottles; 25g, 500g packaged in poly bottles.
• In combination with CuSO 4, has been used as a reagent for the heterogeneous oxidative cyclization of the primary position of a primary-secondary diol to the lactone: J. Chem. Soc., Chem. Commun., 634 (1988); Org, Synth. Coll., 9, 462 (1998):
• The oxidizing power of permanganate can be varied according to the pH of the reaction medium, the use of co-reagents, phase-transfer catalysis, etc. For a comprehensive review of permanganate oxidations in organic chemistry, with particular emphasis on novel applications, see: Synthesis, 85, (1987).
• For phase-transfer oxidation, catalyzed by Tetra-n-butylammonium hydrogen sulfate, A14047, of unfunctionalized benzylic methylenes, or benzylic alcohols to carbonyls, see: Synthesis, 915 (1987). Similar transformations have been carried out in the presence of triethylamine: Synthesis, 293 (1989).
• Classical permanganate cleavage of olefins is difficult to control, and normally proceeds to the highest possible oxidation level. Adsorption of the reagent on moist alumina has been found to attenuate its activity and allow good yields of aldehydes to be obtained. This would appear to provide a possible alternative to ozonolysis for this conversion: J. Org. Chem., 58, 2918 (1993). For use in the cis-hydroxylation of olefins, see Dicyclohexano-18-crown-6, A15344.
• In combination with TMS chloride and benzyl triethylammonium chloride, generates a reagent for mild anti dichlorination of alkenes, conversion of epoxides to chlorohydrins, and selective oxidation of sulfides to sulfoxides: Tetrahedron Lett., 38, 2339 (1997).
dust mask type N95 (US), Eyeshields, full-face particle respirator type N100 (US), Gloves, respirator cartridge type N100 (US), type P1 (EN143) respirator filter, type P3 (EN 143) respirator cartridges
Eyeshields, full-face particle respirator type N100 (US), Gloves, respirator cartridge type N100 (US), type P1 (EN143) respirator filter, type P3 (EN 143) respirator cartridges