mercaptobenzothiazole
- Classification:Rubber accelerator
- Shape:Granules
- Purity:0.99
- Appearance:gray white or light yellow
- Application:Surfactants, Textile Auxiliary Agents
- Keywords:Rubber Chemical Accelerator
- Packing:20kg kraft bags,500kgs/pallet
- Storage:Cool Dry Place
2-mercaptobenzothiazole is an organosulfur compound with the formula c 6 h 4 (nh)sc=s. a white solid, it is used in the sulfur vulcanization of rubber. [1]
karrar mbt tank army recognition,in november 2020, the iranian army has received the latest version of the local-made karrar mbt (main battle tank). the tank had completed all the final trial tests and is now ready to be delivered. karrar mbt variants: no variants at this time
sonocatalytic degradation of 2-mercaptobenzothiazole (mbt) powder
§ study of the sonocatalytic activity of the green maghnite-h sonocatalyst was tested by the degradation of 2-mercaptobenzothiazole (mbt) under ultrasonic irradiation was performed in an ultrasonic bath (frequency of 40 khz, and an ultrasonic power of 120 w) for 120 min at room temperature.
zetax zmbt rubber accelerator chemicals,primary accelerator for natural and synthetic rubbers. nonstaining and non-discoloring. zetax (zmbt) accelerator is used in the same dosages as captax (mbt) accelerator.
2-mercaptobenzothiazole nist chemistry webbook
2-mercaptobenzothiazole. formula: c7h5ns2. molecular weight: 167.251. iupac standard inchi: inchi=1s/c7h5ns2/c9-7-8-5-3-1-2-4-6 (5)10-7/h1-4h, (h,8,9) copy sheet of paper on top of another sheet. iupac standard inchikey: yxiwhuqxzsmyre-uhfffaoysa-n. copy sheet of paper on top of another sheet. cas registry number: 149-30-4.
zmbt (mz) -80ge high speed vulcanization accelerator easily,home chemicals chemical auxiliary catalyst rubber auxiliary agent zmbt (mz) -80ge high speed vulcanization accelerator easily dispersed and yields non-staining and non-discoloring products
2-mercaptobenzothiazole (mbt) chemical supplier for sale
product uses. corrosion inhibitor, latex.
zdec masterbatch (dithiocarbamate accelerator harwick,mixland zdec masterbatch is a fast curing accelerator for nr, sbr, nbr, ir, iir, biir, epdm. it exceeds zdmc in accelerating effects and shows a slight tendency to premature vulcanization. it is also used as a secondary accelerator for all sulfur curable elastomers.
rubber accelerator 2-mercaptobenzothiazole (mbt)
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?
2-mercaptobenzothiazole nist chemistry webbook,molecular weight: 167.251. iupac standard inchi: inchi=1s/c7h5ns2/c9-7-8-5-3-1-2-4-6 (5)10-7/h1-4h, (h,8,9) iupac standard inchikey: yxiwhuqxzsmyre-uhfffaoysa-n. cas registry number: 149-30-4. chemical structure: this structure is also available as a 2d mol file or as a computed 3d sd file. the 3d structure may be viewed using java or javascript.
2-mercaptobenzothiazole nist chemistry webbook,formula: c7h5ns2. molecular weight: 167.251. iupac standard inchi_inchi=1s/c7h5ns2/c9-7-8-5-3-1-2-4-6 (5)10-7/h1-4h, (h,8,9) copy. iupac standard inchikey:yxiwhuqxzsmyre-uhfffaoysa-n copy. cas registry number: 149-30-4.
- 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.
- Who is exposed to MBT?
- In the studies evaluated by the IARC Monographs Working Group, exposure to high amounts of MBT in humans occurred in workers in the chemical industry, but workers in the rubber or tyre-manufacturing industries may also be exposed to MBT.
- Is MBT carcinogenic to humans?
- The Working Group of Volume 115 of the IARC Monographs classified MBT as probably carcinogenic to humans (Group 2A) based on limited evidence of carcinogenicity in humans that it causes bladder cancer, and sufficient evidence of carcinogenicity in experimental animals. What evidence is this classification based on?