| Chemical Properties | Back Directory | [Melting point ]
89.5-90° | [Boiling point ]
567.4±60.0 °C(Predicted) | [density ]
1.42±0.1 g/cm3(Predicted) | [vapor pressure ]
8.5 x l0-8 Pa (25 °C) | [Fp ]
4℃ | [storage temp. ]
0-6°C | [pka]
1.81±0.10(Predicted) | [Water Solubility ]
1.7 mg l-1 (20 °C) |
| Safety Data | Back Directory | [Hazard Codes ]
F,Xn | [Risk Statements ]
11-20/21/22-36 | [Safety Statements ]
16-36/37 | [RIDADR ]
UN 1648 3 / PGII | [WGK Germany ]
2 | [RTECS ]
XZ4803030 | [Toxicity]
LD50 in male, female rats, male, female mice (mg/kg): 2800, 3000, >5000, >5000 orally; in male, female rats (mg/kg): >2000, >2000 dermally; in honey bees (mg/bee): >125 orally; LC50 (48 hr) in carp: 1.02 ppm; LC50 (6 hr) in water fleas: >102 ppm (Ogawa) |
| Hazard Information | Back Directory | [Uses]
Fungicide. | [Uses]
Imibenconazole is used to control scab, powdery mildew, Alternaria
leaf spot, sooty blotch, fly speck and rust on apples, scab and rust on
pears, scab and powdery mildew on fruits, and anthracnose and other
diseases on roses and chrysanthemums. | [Definition]
ChEBI: A member of the class of imidothioates that is the S-4-chlorobenzyl thioester of N-(2,4-dichlorophenyl)-2-(1H-1,2,4-triazol-1-yl)ethanimidothioic acid. Used to control a range of fungal diseases affect
ng fruit, vegetables, turf and ornamentals. It has a low mammalian toxicity and shows a moderate level of toxicity to fish, daphnia and earthworms but is relatively non-toxic to honey bees, birds and algae. | [Metabolic pathway]
There is little published information available on the metabolism of imibenconazole.
Based on the available data (PM) the reaction in Scheme 1 is
proposed. | [Degradation]
Imibenconazole is stable in weak alkali but it is unstable in acidic and in
strongly alkaline conditions (PM). |
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