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Chlorpyrifos 25% + Thiram 25% Ws of Fungicide Pesticide & Repellent Metabolite

China Chlorpyrifos 25% + Thiram 25% Ws of Fungicide Pesticide & Repellent Metabolite, Find details about China Veterinary Substance, Repellent from Chlorpyrifos 25% + Thiram 25% Ws of Fungicide Pesticide & Repellent Metabolite

Model NO.
WS
Chemical Formula 1
C9h11cl3no3PS
CAS 2
137-26-8
Ec No. 2
205-286-2
Chemical Formula 2
C6h12n2s4
Origin
China
Model NO.
WS
Chemical Formula 1
C9h11cl3no3PS
CAS 2
137-26-8
Ec No. 2
205-286-2
Chemical Formula 2
C6h12n2s4
Origin
China
Chlorpyrifos 25% + Thiram 25% WS of Fungicide Pesticide & Repellent Metabolite


Chlorpyrifos
An organophosphate insecticide approved for use in the EU. It has a low aqueous solubility, is quite volatile and is non-mobile. There is a low risk of leaching to groundwater based on its chemical properties. It can be moderately persistent in soil systems but is not usually persistent in water systems. It is highly toxic to mammals, is classified as a reproduction toxicant, an acetyl cholinesterase inhibitor and a neurotoxicant. It is also a skin and eye irritant. It is highly toxic to birds, fish, aquatic inverterbrates and honey bees and moderately toxic to aquatic plants, algae and earthworms

Description: A broad spectrum organophosphorus insecticide and acaricide used to control soil and foliage pests
Example pests controlled: Scale; Wooly aphid; Leaf roller; Caterpillars; Corn earworm; Armyworm; Cutworms; Rootworms; Cockroaches; Flea beetles; Flies; Termites; Fire ants
Example applications: Cereals including barley, wheat; Cotton; Fruit including apples, pears, grapes, pineapples, bananas, strawberries, mango; Tomatoes; Nuts; Vegetables inclding carrots, cabbages, cauliflower, Brussel sprouts

Chemical structure: 
Isomerism-
Chemical formulaC9H11Cl3NO3PS
Canonical SMILESCCOP(=S)(OCC)OC1=NC(=C(C=C1Cl)Cl)Cl
Isomeric SMILESNo data
International Chemical Identifier key (InChIKey)SBPBAQFWLVIOKP-UHFFFAOYSA-N
International Chemical Identifier (InChI)InChI=1S/C9H11Cl3NO3PS/c1-3-14-17(18,15-4-2)16-9-7(11)5-6(10)8(12)13-9/h5H,3-4H2,1-2H3

General status: 
Pesticide typeInsecticide
Substance groupOrganophosphate
Minimum active substance purity970 g/kg
Known relevant impuritiesEU dossier - Sulfotep <3.0 g/kg, Acetone insolubles <5.0 g/kg
Substance originSynthetic
Mode of actionNon-systemic with contact, inhalation and stomach action. Acetylcholinesterase (AChE) inhibitor.
CAS RN2921-88-2
EC number220-864-4
CIPAC number221
US EPA chemical code059101
PubChem CID2730
Molecular mass (g mol-1)350.58
PIN (Preferred Identification Name)O,O-diethyl O-(3,5,6-trichloropyridin-2-yl) phosphorothioate
IUPAC nameO,O-diethyl O-3,5,6-trichloro-2-pyridyl phosphorothioate
CAS nameO,O-diethyl O-(3,5,6-trichloro-2-pyridinyl) phosphorothioate
Other status informationOSPAR soc; WFD priority substance; Marine Pollutant
Relevant Environmental Water Quality StandardsUK Environment Agency non-statutory standard for the protection of aquatic life: Freshwater annual average 0.002 ug/L, max acceptable conc 0.01 ug/L; Saltwater annual average 0.001 ug/L, max acceptable conc 0.01 ug/L




Thiram
Description: A multi-use carbamate fungicide which is also used as a mammal repellent. Also pesticide transformation product.
Example pests controlled: As a fungicide: Seed decay; Seedling blight; Damping-off; Kernal smut; Smuts; Bunts. As a repellent: Rabbits; Deer
Example applications: Cereals including barley, millet, oats, rye, triticale; Beans and peas; Brassicas; Beet crops; Aubergines; Flax; Onions; Soybean; Sunflowers; Tomatoes; Fruit including apples, pear, cherry, strawberry

Chemical structure: 
IsomerismNone
Chemical formulaC6H12N2S4
Canonical SMILESCN(C)C(=S)SSC(=S)N(C)C
Isomeric SMILESNo data
International Chemical Identifier key (InChIKey)KUAZQDVKQLNFPE-UHFFFAOYSA-N
International Chemical Identifier (InChI)InChI=1S/C6H12N2S4/c1-7(2)5(9)11-12-6(10)8(3)4/h1-4H3

General status: 
Pesticide typeFungicide, Repellent, Metabolite
Metabolite TypeSoil, Water, Animal
Substance groupCarbamate
Minimum active substance purity980 g/kg
Known relevant impuritiesEU dossier - None declared
Substance originSynthetic
Mode of actionContact action with protective properties, acts by inhibiting spore germination and mycelial growth. Repellent properties caused by aversion to its taste. Multi-site activity.
CAS RN137-26-8
EC number205-286-2
CIPAC number24
US EPA chemical code079801
PubChem CID5455
Molecular mass (g mol-1)240.43
PIN (Preferred Identification Name)N1,N1,N3,N3-tetramethyl-2-dithioperoxy-1,3-dithiodicarbonic diamide
IUPAC nametetramethylthiuram disulfide
CAS nametetramethylthioperoxydicarbonic diamide
Other status informationChemical subject to PIC regulations (some formulations)

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