| Identification | More | [Name]
Difenzoquat | [CAS]
49866-87-7 | [Synonyms]
1,2-dimethyl-3,5-diphenyl-1h-pyrazolium
1,2-DIMETHYL-3,5-DIPHENYLPYRAZOLIUMION
DIFENZOQUAT
(1,2-dimethyl-3,5-diphenyl)-1h-pyrazoliu
Mataren-Difenzolium(ACC)
1,2-Dimethyl-3,5-diphenylpyrazolium methylsulfate
Methaven
1,2-DIMETHYL-3,5-DIPHENYLPYRAZOLIUM
difenzoquat ion
1,2-Dimethyl-3,5-diphenyl-1H-pyrazol-2-ium
3,5-Diphenyl-1,2-dimethyl-1H-pyrazole-2-ium | [EINECS(EC#)]
256-505-3 | [Molecular Formula]
C17H17N2+ | [MDL Number]
MFCD01941559 | [Molecular Weight]
249.33 | [MOL File]
49866-87-7.mol |
| Hazard Information | Back Directory | [Description]
Difenzoquat is a post-emergence herbicide. Little data is available regarding its environmental fate. It has a low avian toxicity but appears to be more toxic to aquatic species. it is moderately toxic to mammals if ingested and is thought to be an eye irritant. | [Uses]
Difenzoquat bis-Trideuteromethyl Methyl-D3 Perchlorate Salt is the deuterized labeled form of Difenzoquat (D445418), which is a cationic herbicide. | [Definition]
ChEBI: Difenzoquat is a ring assembly and a member of pyrazoles. | [Production Methods]
Difenzoquat is manufactured by one U.S. company
and methods of synthesis are confidential. The product is
available as 2 lb cation per gallon in the United States and
Canada, and internationally at 200–300 g cation per liter and
as solid formulations at 63–65% (w/w) cation. | [Mechanism of action]
Selective, absorbed by foliage. Acts via the rapid destruction of cell membranes. | [Pesticide Type]
Herbicide; Fungicide |
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