China Bactericide Cyazofamid Mancozeb

Chlorothalonil 50% + Dimethomorph 15% WG
Chlorothalonil
Chlorothalonil is a broad spectrum fungicide that is approved for use in the EU and is widely used. It has a low aqueous solubility, is volatile and would not be expected to leach to groundwater. It is slightly mobile. It tends not to be persistent in soil systems but may be persistent in water. It has a low mammalian toxicity but there is some concern regarding its bioaccumulation potential. It is a recognised irritant. Chlorothalonil is moderately toxic to birds, honeybees and earthworms but considered to be more toxic to aquatic organisms.Description:A fungicide used to control a wide range of diseases on a broad range of crops. Also used as a wood preservative.
Example pests controlled:Rust; Fastener & Fitting purple spot; Leaf blight; Anthracnose; Downy mildew; Ring spot; Stalk rot; Botrytis rot; Pod & stem blight
Example applications:Cereals; Vegetables including asparagus, beans, cabbage, cauliflower, broccoli, carrot, onions, celery, curcubits; Corn for seed; Fruit including cranberries, melon;Environment Protection Device Mushrooms; Peanuts; PotatoesChemical structure:IsomerismNoneChemical formulaC8Cl4N2Canonical SMILESC(#N)C1=C(C(=C(C(=C1Cl)Cl)Cl)C#N)ClIsomeric SMILESNo dataInternational Chemical Identifier key (InChIKey)CRQQGFGUEAVUIL-UHFFFAOYSA-NInternational Chemical Identifier (InChI)InChI=1S/C8Cl4N2/c9-5-3(1-13)6(10)8(12)7(11)4(5)2-14
General status:Pesticide typeFungicideSubstance groupChloronitrileMinimum active substance purity985 g/kgKnown relevant impuritiesEU dossier - Hexachlorobenzene 0.04 g/kg; Decachlorobiphenyl 0.03 g/kgSubstance originSyntheticMode of actionNon-systemic, broad-spectrum, foliar action with some protectant properties. Acts by preventing spore germination and zoospore motility. Multi-site activity.CAS RN1897-45-6EC number217-588-1CIPAC number288US EPA chemical code081901PubChem CID15910Molecular mass (g mol-1)265.91PIN (Preferred Identification Name)2,4,5,6-tetrachlorobenzene-1,3-dicarbonitrileIUPAC nametetrachloroisophthalonitrileCAS name2,4,5,6-tetrachloro-1,3-benzenedicarbonitrileOther status information-Relevant Environmental Water Quality StandardsUK Environment Agency non-statutory standard for the protection of aquatic life: freshwater and saltwater annualDemonstrational & Teaching Utensil average 0.1 ug/L, max acceptable conc 1.0 ug/L
Dimethomorph
Description:A fungicide effective against various fungal pathogens in vines and other crops
Example pests controlled:Downy mildew; Anthracnose;, Septoria leaf spot; Late blight; Root rot; Crown rot
Example applications:Curcubits; Grapevines; Head lettuce; Onions; Potatoes; Fruit including blackberries, raspberries, strawberries, grapesChemical structure:IsomerismIsomeric - a mixture of two isomers (E & Z) but only the Z-isomer has fungicidal activityChemical formulaC21H22ClNO4Canonical SMILESCOC1=C(C=C(C=C1)C(=CC(=O)N2CCOCC2)C3=CC=C(C=C3)Cl)OCIsomeric SMILESCOC1=C(C=C(C=C1)/C(=C/C(=O)N2CCOCC2)/C3=CC=C(C=C3)Cl)OCInternational Chemical Identifier key (InChIKey)QNBTYORWCCMPQP-UHFFFAOYSA-NInternMattress Machine ational Chemical Identifier (InChI)InChI=1S/C21H22ClNO4/c1-25-19-8-5-16(13-20(19)26-2)18(15-3-6-17(22)7-4-15)14-21(24)23-9-11-27-12-10-23/h3-8,13-14H,9-12H2,1-2H3/b18-14-
General status:Pesticide typeFungicideSubstance groupMorpholineMinimum active substance purity965 g/kg (E/Z isomer ratio 44/56)Known relevant impuritiesEU dossier - None declaredSubstance originSyntheticMode of actionSystemic with good protective activity. Cellulose synthesis inhibitor.CAS RN110488-70-5EC number404-200-2CIPAC number483US EPA chemical code268800PubChem CID5889665Molecular mass (g mol-1)387.86PIN (Preferred Identification Name)(2EZ)-3-(4-chlorophenyl)-3-(3,4-dimethoxyphenyl)-1-(morpholin-4-yl)prop-2-en-1-oneIUPAC name()-4-[3-(4-chlorophenyl)-3-(3,4-dimethoxyphenyl)acryloyl]morpholineCAS name4-(3-(4-chlorophenyl)Guide Rail -3-(3,4-dimethoxyphenyl)-1-oxo-2-propenyl)morpholine