Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1654593Generated: October 26, 2026

2,5-Dimethyl-2,5-di-(tert-butylperoxy)hexane → tert-Butyl peroxybenzoate

https://huagongshe.com/reaction/1654593

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,5-Dimethyl-2,5-di-(tert-butylperoxy)hexaneHCID 6545—
ReactantDicumyl peroxideHCID 6641—
ReactantBenzoyl PeroxideHCID 7187—
Reactant2,5-Dimethyl-2,5-DI-(benzoylperoxy)hexaneHCID 75796—
Reactant1,1-Bis(tert-butylperoxy)cyclohexaneHCID 76359—
Reactant1,1-Bis(tert-butylperoxy)-3,3,5-trimethylcyclohexaneHCID 93038—
Reactantt-Butylperoxy benzoateHCID 21744378—
Reactant2-Tert-butylperoxy-3,3,5-trimethylhexanoateHCID 21753036—
Reactantt-Butylperoxy(2-ethylhexanoate)HCID 22065482—
Reactantt-Butylperoxyisopropyl carbonateHCID 86748635—
Producttert-Butyl peroxybenzoateHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05408013
Source datasetuspto-grants-1995_04
ORD IDord-b21e0bf705aa4fbc98b3111d4a5a1a59
Source noteuspto-grants-1995_04