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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-(tert-butylperoxy)-3,3,5-trimethylcyclohexane,75%sol.inarom.freemin.spirit;di-tert-butylperoxy-3,3,5-trimethylcyclohexaneperoxide;luperco231g;luperco231xl;1,1-di-(tert-butylperoxy)-3,3,5-trimethylcyclohexane (more than 90%);1,1-di-(tert-butylperoxy)-3,3,5-trimethylcyclohexane (more than 57% but not more than 90%,and diluent type A not less than 10%);1,1-di-(tert-butylperoxy)-3,3,5-trimethylcyclohexane (not more than 32%,and diluent type A not less than 26%,and diluent type B not less than 42%);1,1-di-(tert-butylperoxy)-3,3,5-trimethylcyclohexane (not more than 57%,and diluent type A not less than 43%) | | 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 |
| Melting point | -20 °C | | Boiling point | 403.47°C (rough estimate) | | density | 0.895 | | vapor pressure | 0.009Pa at 20℃ | | refractive index | n20/D 1.441(lit.) | | Fp | 62 °C | | storage temp. | Refrigerator (+4°C) | | solubility | Acetonitrile (Slightly), Chloroform (Sparingly) | | form | Solution | | color | Clear | | Water Solubility | immiscible | | InChI | InChI=1S/C17H34O4/c1-13-10-16(8,9)12-17(11-13,20-18-14(2,3)4)21-19-15(5,6)7/h13H,10-12H2,1-9H3 | | InChIKey | NALFRYPTRXKZPN-UHFFFAOYSA-N | | SMILES | O(C1(CC(C)CC(C)(C)C1)OOC(C)(C)C)OC(C)(C)C | | LogP | 7 at 25℃ | | CAS DataBase Reference | 6731-36-8(CAS DataBase Reference) | | EPA Substance Registry System | Peroxide, 1,1'-(3,3,5-trimethylcyclohexylidene)bis[2-(1,1-dimethylethyl) (6731-36-8) |
| | 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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