Benzoic Acid → HCID 86738909, compound
Reaction equation
[C:1]([O:9][O:10][C:11](=[O:18])[C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1)(=[O:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[C:19]([OH:27])(=[O:26])[C:20]1[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1>>[C:11]([O:10][O:9][C:1](=[O:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1)(=[O:18])[C:12]1[CH:13]=[CH:14][CH:15]=[CH:16][CH:17]=1.[C:19]([OH:27])(=[O:26])[C:20]1[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1Participants
3
Procedure
Employing the acid precipitation processes described in Example II, several other dry free-flowing dibenzoyl peroxide/benzoic acid compositions were prepared which contained 30 to 85% dibenzoyl peroxide and 15 to 70% benzoic acid. The burning characteristics of these invention compositions along with those for 98% dibenzoyl peroxide and for the 50% dibenzoyl peroxide/50% DCHP and the 70% dibenzoyl peroxide/30% DCHP art compositions are summarized in Example III Table.
Workup
- customthe acid precipitation processes
- customwere prepared which
Sources & evidence
- ORD record
- ord-0a6c49997524495f85bfd16da3d02717
- Source dataset
- uspto-grants-1983_06
- Patent number
- US04387044
Reaction notes
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