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].C1(S(OC)(=O)=[O:33])C2C(=CC=CC=2)C=CC=1.[Na].C=O.S([O-])(OCCCCCCCCCCCC)(=O)=O.[Na+]>>[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].[OH2:33]Participants
4
Procedure
2% benziothiazolinone, 73% iprodione, 5% sodium methyl naphthalene sulfonate-formaldehyde condensate, 4% sodium lignosulfonate, 3% sodium dodecyl sulfate, complemented to 100% with diatomite.
Sources & evidence
- ORD record
- ord-7f50cdbcc01f47ef849d7cc3f5e8d17e
- Source dataset
- uspto-grants-2016_03
- Patent number
- US09282744B2
Linked notes
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