| Identification | Back Directory | [Name]
Guazatine acetate salt | [CAS]
115044-19-4 | [Synonyms]
guazatineacetates
Guazatine, acetate
GUAZATINE TRIACETATE
GUAZATINE ACETATE SALT
IMINOCTADINE TRIACETATE
Guazatine acetate (Tech)
guazatinetriacetate(mixtureof
Guazatine acetate @100 μg/mL in MeOH
guazatinetriacetate(mixtureofacetatesofguanidated
guazatinetriacetate(mixtureofacetatesofguanidateddiandtriaminesand | [Molecular Formula]
C24H53N7O6 | [MDL Number]
MFCD01724078 | [MOL File]
115044-19-4.mol | [Molecular Weight]
535.72 |
| Hazard Information | Back Directory | [Uses]
Guazatine is used as a seed treatment for control of Sqtoria
nodorum, Tilletia caries, Fusarium spp. and Helminthosporium spp. in cereals
and maize and it also acts as a bird repellent. It is also used to control
Pyricularia oryzae (rice blast) and Cercuspora spp. in peanuts and soyabeans,
Septoria spp. in wheat and pineapple disease in sugar cane. It is also
used as a post harvest dip for seed potatoes, citrus fruit and pineapples
and as a wood protectant. | [Definition]
ChEBI: Iminoctadine is a member of the class of guanidines that is dioctylamine in which a hydrogen from each of the terminal methyl groups is replaced by a guanidino group. Once used as a fungicidal seed dressing, it is no longer approved for use in the European Union. It has a role as an antifungal agrochemical. It is a member of guanidines, a secondary amino compound and an aliphatic nitrogen antifungal agent. | [Metabolic pathway]
The deamidation of guazatine (GZ) is a primary mode
of GZ-biotransformation in rats but is not significantly
mediated by either hydrolysis or transamidation to
glycine or ornithine. In photolysis, Pm is formed by
photooxidation of the methylene group (probably at the
3 or 5 position). One of the minor photoproducts
identified is considered to be an intermediate of Pm
formation. In apple plants, the same degradation
products are identified on the surface of the leaves as
photodegradation products. |
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