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Thiophanat-ethyl

Thiophanat-ethyl Suppliers list
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Thiophanat-ethyl Basic information
Product Name:Thiophanat-ethyl
Synonyms:1,2-BIS(3-ETHOXYCARBONYL-2-THIOUREIDO) BENZENE;DIETHYL 4,4'-O-PHENYLENEBIS(3-THIO-ALLOPHANATE);DIETHYL 4,4'-O-PHENYLENEBIS(3-THIOALLOPHANATEL);CERCOBIN;LABOTEST-BB LT00134857;TOPSIN E;(1,2-phenylenebis(iminocarbonothioyl))bis-carbamicacidiethylester;1,2-di-(3-Ethoxycarbonyl-2-thioureido)benzene
CAS:23564-06-9
MF:C14H18N4O4S2
MW:370.45
EINECS:245-741-2
Product Categories:Alpha sort;BenzimidazolesPesticides;CarbamatesPesticides&Metabolites;Fungicides;Pesticides;Q-ZAlphabetic;TF - TO
Mol File:23564-06-9.mol
Thiophanat-ethyl Structure
Thiophanat-ethyl Chemical Properties
Melting point 195°C
density 1.3709 (rough estimate)
refractive index 1.6000 (estimate)
storage temp. 0-6°C
pka6.37±0.70(Predicted)
Henry's Law Constant1.9×107 mol/(m3Pa) at 25℃, HSDB (2015)
CAS DataBase Reference23564-06-9(CAS DataBase Reference)
EPA Substance Registry SystemThiophanate-ethyl (23564-06-9)
Safety Information
HS Code 29309090
Hazardous Substances Data23564-06-9(Hazardous Substances Data)
ToxicityLD50 orally in mice and rats: >15 g/kg (Eichler)
MSDS Information
Thiophanat-ethyl Usage And Synthesis
UsesTHIOPHANAT-ETHYL is a broad-spectrum systemic fungicide used to control powdery mildew, wheat scab, rapeseed sclerotinia, tomato leaf mold, and other diseases in various plants.
Production MethodsCommercial 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
DefinitionChEBI: 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 DescriptionColorless crystals. Non corrosive.
Air & Water ReactionsHydrolyzed by alkaline media.
Reactivity ProfileTHIOPHANAT-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.
Mechanism of actionInhibition of mitosis and cell division (Beta-tubulin assembly in mitosis)
Pesticide TypeFungicide
Thiophanat-ethyl Preparation Products And Raw materials
Tag:Thiophanat-ethyl(23564-06-9) Related Product Information
Colistin sulfate Thiourea noxytiolin 2-(3-Methoxycarbonylthioureido)aniline Methylmethoxythiourea Thiophanat-ethyl Benzene Thiophanate-methyl