| Identification | More | [Name]
THIOPHANAT-ETHYL | [CAS]
23564-06-9 | [Synonyms]
1,2-BIS(3-ETHOXYCARBONYL-2-THIOUREIDO) BENZENE
CERCOBIN
DIETHYL 4,4'-O-PHENYLENEBIS(3-THIO-ALLOPHANATE)
DIETHYL 4,4'-O-PHENYLENEBIS(3-THIOALLOPHANATEL)
LABOTEST-BB LT00134857
THIOPHANATE
THIOPHANATE-ETHYL
THIOPHANAT-ETHYL
TOPSIN E
(1,2-phenylenebis(iminocarbonothioyl))bis-carbamicacidiethylester
1,2-di-(3-Ethoxycarbonyl-2-thioureido)benzene
1,2-Phenylenebis(iminocarbonothioyl)biscar-bamicacid
3336-f
3336turffungicide
4,4’-o-phenylenebis(3-thio-allophanicacidiethylester
bas3220
Carbamicacid,[1,2-phenylenebis-(iminocarbonothioyl)]bis-,diethylester
cercobinwp50%
cerobin
chipcospotkleen | [EINECS(EC#)]
245-741-2 | [Molecular Formula]
C14H18N4O4S2 | [MDL Number]
MFCD00128010 | [Molecular Weight]
370.45 | [MOL File]
23564-06-9.mol |
| Hazard Information | Back Directory | [General Description]
Colorless crystals. Non corrosive. | [Reactivity Profile]
THIOPHANATE ETHYL(23564-06-9) 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. | [Air & Water Reactions]
Hydrolyzed by alkaline media. | [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. | [Production Methods]
Commercial production of thiophanate is described mainly through industrial routes for thiophanate methyl, the principal commercial form. Manufacture begins with o phenylenediamine and sodium thiocyanate, which undergo a thiocyanation–condensation reaction to form the benzimidazole dithiocarbamate core. The process typically uses solvents such as ethyl acetate to dissolve reactants efficiently and shorten reaction time. After condensation, the mixture is neutralised, wastewater is treated or recycled, and the crude product is isolated by filtration or centrifugation | [Mechanism of action]
Inhibition of mitosis and cell division (Beta-tubulin assembly in mitosis) | [Pesticide Type]
Fungicide |
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