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| | 1,1-Di-(tert-butylperoxy)-3,3,5-trimethylcyclohexane Basic information |
| Product Name: | 1,1-Di-(tert-butylperoxy)-3,3,5-trimethylcyclohexane | | Synonyms: | 1,1-di(butylperoxy)-3,3,5-trimethylcyclohexane;1,1-di-(tert-butylperoxy)-3,3,5-trimethylcyclohexane,75%sol.inarom.freemin.spirit;di-tert-butylperoxy-3,3,5-trimethylcyclohexaneperoxide;luperco231g;luperco231xl;luperco231xlp;lupersol231;perhexa3m | | CAS: | 6731-36-8 | | MF: | C17H34O4 | | MW: | 302.46 | | EINECS: | 229-782-3 | | Product Categories: | Organics | | Mol File: | 6731-36-8.mol |  |
| | 1,1-Di-(tert-butylperoxy)-3,3,5-trimethylcyclohexane Chemical Properties |
| | 1,1-Di-(tert-butylperoxy)-3,3,5-trimethylcyclohexane Usage And Synthesis |
| Chemical Properties | clear solution | | Uses | 1,1-Di-tert-butylperoxy-3,5,5-trimethylcyclohexane is a crosslinking agent that may be used in polymerization reactions. | | Reactivity Profile | Peroxides, such as 1,1-DI-(TERT-BUTYLPEROXY)-3,3,5-TRIMETHYL CYCLOHEXANE, are good oxidizing agents. Organic compounds can ignite on contact with concentrated peroxides. Strongly reduced material such as sulfides, nitrides, and hydrides may react explosively with peroxides. There are few chemical classes that do not at least produce heat when mixed with peroxides. Many produce explosions or generate gases (toxic and nontoxic). Generally, dilute solutions of peroxides (<70%) are safe, but the presence of a catalyst (often a transition metal such as cobalt, iron, manganese, nickel, or vanadium) as an impurity may even then cause rapid decomposition, a buildup of heat, and even an explosion. Solutions of peroxides often become explosive when evaporated to dryness or near-dryness. May explode from heat or contamination. | | Flammability and Explosibility | Flammable |
| | 1,1-Di-(tert-butylperoxy)-3,3,5-trimethylcyclohexane Preparation Products And Raw materials |
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