| Identification | Back Directory | [Name]
PROCYAZINE | [CAS]
32889-48-8 | [Synonyms]
Cycle
CYCLE(R)
CGA-18762
PROCYAZINE
procyanazine
Cycle (herbicide)
Procyazine Solution in Methanol, 100μg/mL
2-(4-Chloro-6-(cyclopropylamino)-s-triazin-2-yl)amino-2-methylpropionitrile
2-(4-chloro-6-(cyclopropylamino)-s-triazin-2-ylamino)-2-methyl-propionitril
2-((4-chloro-6-(cyclopropylamino)-1,3,5-triazin-2-yl)amino)-2-methylpropanen
Propionitrile, 2-[[4-chloro-6-(cyclopropylamino)-s-triazin-2-yl]amino]-2-methyl-
2-[[-4-CHLORO-6-(CYCLOPROPYLAMINO)-1,3,5-TRIAZIN-2-YL]-AMINO]-2-METHYLPROPANENITRILE
Propanenitrile, 2-[[4-chloro-6-(cyclopropylamino)-1,3,5-triazin-2-yl]amino]-2-methyl- | [Molecular Formula]
C10H13ClN6 | [MDL Number]
MFCD00155445 | [MOL File]
32889-48-8.mol | [Molecular Weight]
252.7 |
| Hazard Information | Back Directory | [Chemical Properties]
Crystalline solid; melts at 170 °C (338 °F);aqueous solubility data not available; dissolves in organic solvents. | [Production Methods]
The commercial synthesis of procyazine involves the cyclisation of cyanuric chloride with cyclopropylamine, followed by substitution with a branched alkyl nitrile such as 2-amino-2-methylpropanenitrile. This yields the active compound. | [Health Hazard]
Oral toxicity in rates was found to be moderate; possibly toxic by other routes of exposures; contains a nitrile functional group andis structurally related to cyanazine; moderately toxic by skin absorption; teratogeniceffect in experimental animals.
LD50 oral (rat): 290 mg/kg. | [Mechanism of action]
Selective, systemic action with residual and foliar activity. Inhibits photosynthesis (photosystem II). | [Pesticide Type]
Herbicide |
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