Bromoxynil 125g/L + Diflufenican 40g/L + Ioxynil 75g/L Ec Herbicide Pesticide & Metabolite

China Bromoxynil 125g/L + Diflufenican 40g/L + Ioxynil 75g/L Ec Herbicide Pesticide & Metabolite, Find details about China Weedicide, Chlorimuron-Ethyl from Bromoxynil 125g/L + Diflufenican 40g/L + Ioxynil 75g/L Ec Herbicide Pesticide & Metabolite

Model NO.
EC
Chemical Formula 1
C7h3br2no
CAS 2
83164-33-4
Chemical Formula 2
C19h11f5n2o2
CAS 3
1689-83-4
Ec Number 2
216-881-1
Chemical Formula 3
C7h3I2no
Origin
China
Model NO.
EC
Chemical Formula 1
C7h3br2no
CAS 2
83164-33-4
Chemical Formula 2
C19h11f5n2o2
CAS 3
1689-83-4
Ec Number 2
216-881-1
Chemical Formula 3
C7h3I2no
Origin
China
Bromoxynil 125g/l + Diflufenican 40g/l + Ioxynil 75g/l EC of Herbicide Pesticide & Metabolite


Bromoxynil

A widely used herbicide approved for use in the EU. It has a high aqueous solubility and is not considered to be volatile. The potential for leaching to groundwater is considered low, and it is not expected to be persistent in soil or water systems. It is highly toxic to mammals, is an endocrine distrupter and may cause negative reproduction or development effects. It is moderately toxic to most aquatic and terrestrial biodviersity. The main exceptions are a low toxicity to algae and honeybees by the contact route (not the oral route).

Description: An HBN herbicide used for post-emergence control of annual broad-leaved weeds. it is also a pesticide transformation product
Example pests controlled: Pigweed; Mayweed; Knotweed; Shepherd's purse; Goosefoot; Morning glory; Dwarf marigold; Stinkweed; Cocklebur; Wild radish
Example applications: Cereals including wheat, barley, oats; Lucerne; Corn; Sorghum; Onions; Flax; Mint; Turf; Non-crop land


Chemical structure: 
IsomerismNone
Chemical formulaC7H3Br2NO
Canonical SMILESC1=C(C=C(C(=C1Br)O)Br)C#N
Isomeric SMILESNo data
International Chemical Identifier key (InChIKey)UPMXNNIRAGDFEH-UHFFFAOYSA-N
International Chemical Identifier (InChI)InChI=1S/C7H3Br2NO/c8-5-1-4(3-10)2-6(9)7(5)11/h1-2,11H

General status: 
Pesticide typeHerbicide, Metabolite
Metabolite TypeSoil
Substance groupHydroxybenzonitrile
Minimum active substance purity970 g/kg
Known relevant impuritiesEU dossier - None declared
Substance originSynthetic
Mode of actionSelective, contact action with some systemic activity. Inhibits photosynthesis (photosystem II).
CAS RN1689-84-5
EC number216-882-7
CIPAC number87
US EPA chemical code035301
PubChem CID15531
Molecular mass (g mol-1)276.9
PIN (Preferred Identification Name)3,5-dibromo-4-hydroxybenzonitrile
IUPAC name3,5-dibromo-4-hydroxybenzonitrile
CAS name3,5-dibromo-4-hydroxybenzonitrile
Other status informationMarine Pollutant; PAN listed Highly Hazardous Chemical
Relevant Environmental Water Quality StandardsUK Environment Agency non-statutory standard for the protection of aquatic life: freshwater and saltwater annual average 100 ug/L; max acceptable conc: 1000 ug/L






Diflufenican
Description: A herbicide used to control grasses and broad-leaved weeds often used in mixtures
Example pests controlled: Wild radish; Hedge mustard; Charlock; Prickly lettuce; Chickweed; Loosestrife; Stinging nettles
Example applications: Clover-based pastures; Field peas; Lentils; Lupins; Winter cereals

Chemical structure: 
Isomerism-
Chemical formulaC19H11F5N2O2
Canonical SMILESC1=CC(=CC(=C1)OC2=C(C=CC=N2)C(=O)NC3=C(C=C(C=C3)F)F)C(F)(F)F
Isomeric SMILESNo data
International Chemical Identifier key (InChIKey)WYEHFWKAOXOVJD-UHFFFAOYSA-N
International Chemical Identifier (InChI)InChI=1S/C19H11F5N2O2/c20-12-6-7-16(15(21)10-12)26-17(27)14-5-2-8-25-18(14)28-13-4-1-3-11(9-13)19(22,23)24/h1-10H,(H,26,27)

General status: 
Pesticide typeHerbicide
Substance groupCarboxamide
Minimum active substance purity970 g/kg
Known relevant impuritiesEU dossier - None declared
Substance originSynthetic
Mode of actionSelective contact and residual action. Bleaching: inhibition of carotenoid biosynthesis.
CAS RN83164-33-4
EC number-
CIPAC number462
US EPA chemical code-
PubChem CID91735
Molecular mass (g mol-1)394.29
PIN (Preferred Identification Name)N-(2,4-difluorophenyl)-2-[3-(trifluoromethyl)phenoxy]pyridine-3-carboxamide
IUPAC name2',4'-difluoro-2-(α,α,α-trifluoro-m-tolyloxy)nicotinanilide
CAS nameN-(2,4-difluorophenyl)-2-[3-(trifluoromethyl)phenoxy]-3-pyridinecarboxamide




Ioxynil
Description: A herbicide used for post-emergence control of various weeds. Also pesticide transformation product.
Example pests controlled: Annual broad-leaved weeds
Example applications: Cereals; Onions; Leeks; Garlic; Shallots; Flax; Sugarcane; Forage grasses; Lawns & turf

Chemical structure: 
IsomerismNone
Chemical formulaC7H3I2NO
Canonical SMILESC1=C(C=C(C(=C1I)O)I)C#N
Isomeric SMILESNo data
International Chemical Identifier key (InChIKey)NRXQIUSYPAHGNM-UHFFFAOYSA-N
International Chemical Identifier (InChI)InChI=1S/C7H3I2NO/c8-5-1-4(3-10)2-6(9)7(5)11/h1-2,11H

General status: 
Pesticide typeHerbicide, Metabolite
Metabolite TypeSoil
Substance groupHydroxybenzonitrile
Minimum active substance purity960 g/kg
Known relevant impuritiesEU dossier - None declared
Substance originSynthetic
Mode of actionSelective, systemic with contact action, acts by inhibiting photosynthesis at Photosystem II
CAS RN1689-83-4
EC number216-881-1
CIPAC number86
US EPA chemical code353200
PubChem CID15530
Molecular mass (g mol-1)370.91
PIN (Preferred Identification Name)-
IUPAC name4-hydroxy-3,5-diiodophenyl cyanide
CAS name4-hydroxy-3,5-diiodobenzonitrile
Other status informationMarine Pollutant
Relevant Environmental Water Quality StandardsUK Environment Agency non-statutory standard for the protection of freshwater and saltwater aquatic life: 10 ug/L as annual average; 100 ug/L as max acceptable conc.]