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| | 2-sec-Butyl-4,6-dinitrophenol triethanolamine salt Basic information |
| Product Name: | 2-sec-Butyl-4,6-dinitrophenol triethanolamine salt | | Synonyms: | 2-(1-methyl-n-propyl)-4,6-dinitrophenoltriethanolaminesalt;2-sec-butyl-4,6-dinitrophenol2,2’,2’’-nitrilotriethanolsalt;dinitrobutylphenol2,2’,2’’-nitrilotriethanolsalt;dinoseb,triethanolaminesalt;ol](1:1);o-sec-butyl-4,6-dinitrophenoltriethanolaminesalt;phenol,2-(1-methylpropyl)-4,6-dinitro-,compd.with2,2’,2’’-nitrilotris[ethan;phenol,2-sec-butyl-4,6-dinitro-,2,2’,2’’-nitrilotriethanolsalt | | CAS: | 6420-47-9 | | MF: | C16H27N3O8 | | MW: | 389.4 | | EINECS: | 229-166-4 | | Product Categories: | | | Mol File: | 6420-47-9.mol |  |
| | 2-sec-Butyl-4,6-dinitrophenol triethanolamine salt Chemical Properties |
| | 2-sec-Butyl-4,6-dinitrophenol triethanolamine salt Usage And Synthesis |
| Uses | Herbicide; insecticide; miticide. | | Production Methods | Dinoseb trolamine was produced through the same two-stage logic that underpinned all dinoseb salts: first generate the parent nitrophenol, then neutralise it with the chosen base. Manufacturers began with mixed-acid nitration of 2-tert-butylphenol to obtain technical dinoseb, followed by careful purification to strip out residual acids and minimise the oxidative darkening that nitrophenols undergo if impurities remain. The purified dinoseb was then reacted with triethanolamine, commonly called “trolamine”, in an aqueous or hydroalcoholic medium. | | Mechanism of action | Inhibits respiratory electron transport, and uncouples oxidative phosphorylation - membrane disruption. Selective, non-systemic. Contact action. | | Pesticide Type | Herbicide |
| | 2-sec-Butyl-4,6-dinitrophenol triethanolamine salt Preparation Products And Raw materials |
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