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| | THIOPHANAT-ETHYL Basic information |
| | THIOPHANAT-ETHYL Chemical Properties |
| | THIOPHANAT-ETHYL Usage And Synthesis |
| Definition | ChEBI: A member of the class of thioureas that is the diethyl ester of (1,2-phenylenedicarbamothioyl)biscarbamic acid. A fungicide effective against a broad spectrum of diseases in fruit, vegetables, turf and other crops including eyespot, scab, powdery mildew an
grey mould. | | General Description | Colorless crystals. Non corrosive. | | Air & Water Reactions | Hydrolyzed by alkaline media. | | Reactivity Profile | THIOPHANAT-ETHYL is a carbamate ester. Carbamates are chemically similar to, but more reactive than amides. Like amides they form polymers such as polyurethane resins. Carbamates are incompatible with strong acids and bases, and especially incompatible with strong reducing agents such as hydrides. Flammable gaseous hydrogen is produced by the combination of active metals or nitrides with carbamates. Strongly oxidizing acids, peroxides, and hydroperoxides are incompatible with carbamates. This substance is incompatible with copper containing compounds. |
| | THIOPHANAT-ETHYL Preparation Products And Raw materials |
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