HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,5-Dimethyl-2,5-di-(tert-butylperoxy)hexane → tert-Butyl peroxybenzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,5-Dimethyl-2,5-di-(tert-butylperoxy)hexane | HCID 6545 | — |
| Reactant | Dicumyl peroxide | HCID 6641 | — |
| Reactant | Benzoyl Peroxide | HCID 7187 | — |
| Reactant | 2,5-Dimethyl-2,5-DI-(benzoylperoxy)hexane | HCID 75796 | — |
| Reactant | 1,1-Bis(tert-butylperoxy)cyclohexane | HCID 76359 | — |
| Reactant | 1,1-Bis(tert-butylperoxy)-3,3,5-trimethylcyclohexane | HCID 93038 | — |
| Reactant | t-Butylperoxy benzoate | HCID 21744378 | — |
| Reactant | 2-Tert-butylperoxy-3,3,5-trimethylhexanoate | HCID 21753036 | — |
| Reactant | t-Butylperoxy(2-ethylhexanoate) | HCID 22065482 | — |
| Reactant | t-Butylperoxyisopropyl carbonate | HCID 86748635 | — |
| Product | tert-Butyl peroxybenzoate | HCID 11966 | — |
Reaction Steps
As the polymerization initiator, organic peroxides such as 1,1-bis(t-butylperoxy)-3,3,5-trimethylcyclohexane, 1,1-bis(t-butylperoxy)cyclohexane, t-butylperoxy-3,3,5-trimethylhexanoate, t-butylperoxyisopropyl carbonate, 2,5-dimethyl-2,5-di(benzoylperoxy)hexane, t-butylperoxy benzoate, dicumylperoxide, 2,5-dimethyl-2,5-di(t-butyl peroxy)hexane, t-butylperoxy(2-ethylhexanoate), di-t-butyl hydroperoxide, t-butylperoctoate, benzoylperoxide, etc. are used. In order to obtain a superior surface quality in a usual molding time, t-butyl-peroxybenzoate alone or in an admixture with another compound is preferably used.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05408013 |
| Source dataset | uspto-grants-1995_04 |
| ORD ID | ord-b21e0bf705aa4fbc98b3111d4a5a1a59 |
| Source note | uspto-grants-1995_04 |