Sino Agro-Chemical Industry Ltd.  

Product Name: Imidacloprid 20% + metalaxyl-M 20% + Tebuconazole 2% Ws of Fungicide Pesticide Model NO.: WS Composition: Organic Conductivity: Systemic Fungicide Application Fields: Agricultural Fungicide Application: Fungicide Appearance: Powder CAS 1: 105827-78-9 M.F. 1: C9h10cln5o2 CAS 2: 70630-17-0 M.F. 2: C15h21no4 CAS 3: 107534-96-3 M.F. 3: C16h22cln3o Ec No. 3: 403-640-2 Origin: China Product Description Imidacloprid 20% +metalaxyl-M 20% +Tebuconazole 2% WSImidaclopridImidacloprid is an insecticide approved for use in the EU with certain restrictions for flowering crops. It is highly soluble, non-volatile and persistent in soil. It is moderately mobile. It has alow risk of bioaccumulating. It is highly toxic to birds and honeybees. Moderately toxic to mammals and earthworms. It is non-toxic to fish.Description:A chloronicotine insecticide used to control sucking and soil insects. Also used as aflea treatment for domestic pets.Example pests controlled:Plant hoppers, Aphids, Termites, Colorado bettle, Fleas, White grups, Craneflies; Crickets, AntsExample applications:Lawns and turf; Domestic pets; Rice, Cereals; Maize; Potatoes; Sugar beetChemical structure:IsomerismIsomeric -existing as both the E- and Z- forms however many commerical products are comprised of almost entirely the (E)-isomerChemical formulaC9H10ClN5O2Canonical SMILESC1CN(C(=N1)N[N+](=O)[O-])CC2=CN=C(C=C2)ClIsomeric SMILESNo dataInternational Chemical Identifier key (InChIKey)YWTYJOPNNQFBPC-UHFFFAOYSA-NInternational Chemical Identifier (InChI)InChI=1S/C9H10ClN5O2/c10-8-2-1-7(5-12-8)6-14-4-3-11-9(14)13-15(16)17/h1-2, 5H, 3-4, 6H2, (H, 11, 13)General status:Pesticide typeInsecticide, Veterinary substanceSubstance groupNeonicotinoidMinimum active substance purity970 g/kgKnown relevant impuritiesEU dossier -None declaredSubstance originSyntheticMode of actionSystemic with contact and stomach action. Acetylcholine receptor (nAChR) agonist.CAS RN138261-41-3EC number-CIPAC number582US EPA chemical code129099PubChem CID86418Molecular mass (g mol-1)255.66PIN (Preferred Identification Name)-IUPAC name(E)-1-(6-chloro-3-pyridylmethyl)-N-nitroimidazolidin-2-ylideneamineCAS name(2E)-1-((6-chloro-3-pyridinyl)methyl)-N-nitro-2-imidazolidinimineOther status informationNOTE ban or usage restriction may be in place for use on flowering crops in some Member Statesmetalaxyl-MDescription:A fungicide used to control diseases caused by air- and soil-borne pathogensExample pests controlled:Foliar and tuber blight; Downey mildews;Pseudoperonospora humuli;Phytophthora infestans;Peronospora tabacinaExample applications:Potatoes; Tomatoes; Hops; Lettuce; Vegetables; TobaccoChemical structure:Isomerismmetalaxyl-M is the biologically active enantiomer (R-form) of the isomeric compound metalaxylChemical formulaC15H21NO4Canonical SMILESCC1=C(C(=CC=C1)C)N(C(C)C(=O)OC)C(=O)COCIsomeric SMILESNo dataInternational Chemical Identifier key (InChIKey)ZQEIXNIJLIKNTD-GFCCVEGCSA-NInternational Chemical Identifier (InChI)InChI=1S/C15H21NO4/c1-10-7-6-8-11(2)14(10)16(13(17)9-19-4)12(3)15(18)20-5/h6-8, 12H, 9H2, 1-5H3/t12-/m1/s1General status:Pesticide typeFungicideSubstance groupPhenylamideMinimum active substance purity910 g/kgKnown relevant impuritiesEU dossier -2, 6-dimethyl-phenylamine; 4-methoxy-5-methyl-5H-(1, 2)oxathiole 2, 2-dioxide; 1-methoxy-1-oxopropan-2-yl N-(2, 6-dimethylphenyl)-N-(methoxyacetyl)alaninateSubstance originSyntheticMode of actionSystemic with curative and protective action. Disrupts fungal nucleic acid synthesis -RNA ploymerase 1.CAS RN70630-17-0EC number-CIPAC number580US EPA chemical code-PubChem CID11150163Molecular mass (g mol-1)279.33PIN (Preferred Identification Name)-IUPAC nameMethylN-(methoxyacetyl)-N-(2, 6-xylyl)-D-alaninateCAS nameMethylN-(2, 6-dimethylphenyl)-N-(methoxyacetyl)-D-alaninateTebuconazoleDescription:A fungicide effective against various foliar diseases in cereals and other field cropsExample pests controlled:Smut; Bunt; Stripe rust; Yellow leaf spot; Powdery mildew; Scelerotinia rot; Black spot; Net blotchExample applications:Cereals including wheat, barley, oat, rye; Grapes; Peanuts; Vegetables including onions, peas, pepper; Bananas; SugarcaneChemical structure:IsomerismA chiral molecule. The technical material is an isomeric mixture of the (S-) and (R-) isomers. The R-form is more biologically active than the S-form.Chemical formulaC16H22ClN3OCanonical SMILESCC(C)(C)C(CCC1=CC=C(C=C1)Cl)(CN2C=NC=N2)OIsomeric SMILESNo dataInternational Chemical Identifier key (InChIKey)PXMNMQRDXWABCY-UHFFFAOYSA-NInternational Chemical Identifier (InChI)InChI=1S/C16H22ClN3O/c1-15(2, 3)16(21, 10-20-12-18-11-19-20)9-8-13-4-6-14(17)7-5-13/h4-7, 11-12, 21H, 8-10H2, 1-3H3General status:Pesticide typeFungicide, Plant growth regulatorSubstance groupTriazoleMinimum active substance purity950 g/kgKnown relevant impuritiesEU dossier -None declaredSubstance originSyntheticMode of actionSystemic with protective, curative and eradicant action. Disrupts membrane function. Sterol biosynthesis inhibitor.CAS RN107534-96-3EC number403-640-2CIPAC number494US EPA chemical code128997PubChem CID86102Molecular mass (g mol-1)307.82PIN (Preferred Identification Name)Rac-(3R)-1-(4-chlorophenyl)-4, 4-dimethyl-3-(1H-1, 2, 4-triazol-1-ylmethyl)pentan-3-olIUPAC name(RS)-1-p-chlorophenyl-4, 4-dimethyl-3-(1H-1, 2, 4-triazol-1-ylmethyl)pentan-3-olCAS nameΑ-(2-(4-chlorophenyl)ethyl)-α-(1, 1-dimethylethyl)-1H-1, 2, 4-triazole-1-ethanol