Reaction equation
[CH3:1][CH:2]([NH:4][C:5]([N:7]1[C:12](=[O:13])[N:11]([C:14]2[CH:15]=[C:16]([Cl:21])[CH:17]=[C:18]([Cl:20])[CH:19]=2)[C:9](=[O:10])[CH2:8]1)=[O:6])[CH3:3].C(S([O-])(=O)=[O:35])CCCCCCCCCCC.[Na+].S([O-])([O-])(=O)=O.[NH4+].[NH4+].C(=O)([O-])[O-].[Ca+2]>>[CH3:3][CH:2]([NH:4][C:5]([N:7]1[C:12](=[O:13])[N:11]([C:14]2[CH:19]=[C:18]([Cl:20])[CH:17]=[C:16]([Cl:21])[CH:15]=2)[C:9](=[O:10])[CH2:8]1)=[O:6])[CH3:1].[OH2:35]Participants
5
Procedure
60% benziothiazolinone, 2% iprodione, 2% sodium dodecyl sulfonate, 2% sodium alkyl naphthalene sulfonate, 3% ammonium sulfate, complemented to 100% with light calcium carbonate.
Sources & evidence
- ORD record
- ord-50f33e312f1241cfa3dabeafce811182
- Source dataset
- uspto-grants-2016_03
- Patent number
- US09282744B2
Linked notes
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