CN105284853A - Corn field herbicide - Google Patents

Corn field herbicide Download PDF

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Publication number
CN105284853A
CN105284853A CN201510746490.4A CN201510746490A CN105284853A CN 105284853 A CN105284853 A CN 105284853A CN 201510746490 A CN201510746490 A CN 201510746490A CN 105284853 A CN105284853 A CN 105284853A
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CN
China
Prior art keywords
corn field
sulphur
ketone
grand
herbicide
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Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
CN201510746490.4A
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Chinese (zh)
Inventor
王礼文
刘鹏
冷忠国
陈佛祥
朱刚
张志伟
吴泽伟
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Guangdong Zhongxun Agri Science Corp
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Guangdong Zhongxun Agri Science Corp
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Application filed by Guangdong Zhongxun Agri Science Corp filed Critical Guangdong Zhongxun Agri Science Corp
Priority to CN201510746490.4A priority Critical patent/CN105284853A/en
Publication of CN105284853A publication Critical patent/CN105284853A/en
Priority to CN201610701058.8A priority patent/CN106359428A/en
Pending legal-status Critical Current

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    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N47/00Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
    • A01N47/08Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
    • A01N47/28Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N<
    • A01N47/36Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N< containing the group >N—CO—N< directly attached to at least one heterocyclic ring; Thio analogues thereof
    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N41/00Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a sulfur atom bound to a hetero atom
    • A01N41/02Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a sulfur atom bound to a hetero atom containing a sulfur-to-oxygen double bond
    • A01N41/10Sulfones; Sulfoxides
    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/34Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
    • A01N43/40Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom six-membered rings

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  • Life Sciences & Earth Sciences (AREA)
  • Agronomy & Crop Science (AREA)
  • Pest Control & Pesticides (AREA)
  • Plant Pathology (AREA)
  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Dentistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Wood Science & Technology (AREA)
  • Zoology (AREA)
  • Environmental Sciences (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)

Abstract

The invention discloses corn field herbicide. The corn field herbicide includes effective components of tembotrione, thiencarbazone-methyl and aminopyralid (or ester compound of the aminopyralid). The corn field herbicide is prepared from, by weight, 1%-30% of the tembotrione, 1%-30% of the thiencarbazone-methyl, 1%-40% of the aminopyralid (or the ester compound of the aminopyralid) and the balance herbicide auxiliaries. The corn field herbicide has the advantages that after the tembotrione, the thiencarbazone-methyl and the aminopyralid (or the ester compound of the aminopyralid) are compounded, the weeding effect is improved, and the weeding spectrum is widened; poison and residues are low, the drug use amount, drug use frequency and the using cost are lowered obviously, the effect of the composition is obviously higher than the effects of all single components, and the corn field herbicide is good novel composition pesticide for preventing and killing annual weeds in a corn field.

Description

Corn field herbicide
Technical field
The present invention relates to a kind of corn field herbicide, be, chlorine Fampridine acid (or its ester type compound) grand with ring sulphur ketone, thiophene ketone sulphur for active ingredient, for preventing and kill off corn field annual weed.
Background technology
Ring sulphur ketone (tembotrione), it is a kind of three ketones selective herbicide, effectively can prevent and treat main broadleaved herb and some grassy weeds, as piemarker, three-coloured amaranth, lamb's-quarters, knotweed, barnyard grass, lady's-grass etc. have good control efficiency, can be used for cauline leaf process after Seal treatment and bud before bud.
Thiophene ketone sulphur grand (thiencarbazone-methyl) is sulfonyl-amino-carbnyl triazolinone class weed killer herbicide, is inhibitor of acetolactate synthetase.Thiophene ketone sulphur is grand is effectively can prevent and kill off corn field grassy weed as lady's-grass, eleusine indica, barnyard grass, green foxtail etc. and most of broad leaved weed, registration is used for corn (land for growing field crops, sweet corn, popcorn), wheat and be used for preventing and kill off annual weed on the lawn of residence area and ornamental plants, all can use in early days before bud and after bud, after bud, using dosage is far below using dosage before bud.
Chlorine Fampridine acid (aminopyralid), is picolinic acid class new herbicides, is mainly used in preventing and kill off annual and perennial broad leaved weed, is widely used in mountain region, grassland, the preventing and kill off of planting site and uncultivated area weeds.The different monooctyl ester of fluroxypyr (Fluroxypyr-meptyl) for pyridine fluoroacetic acid class weed killer herbicide be hormone herbicide, can be conducted by the blade of plant and root absorption, make plant deformity, distortion is dead, mainly prevents and kill off annual broadleaf weed, invalid to grassy weed.The different monooctyl ester of fluroxypyr prevents and kill off broad leaved weed as broad leaved weeds such as clearvers, chickweed, field bindweed, kitchen garden, water peanut, acalypha copperleafs with being applicable to gramineous crop field and fruit-bearing forest tea.
The present inventor is grand to ring sulphur ketone, thiophene ketone sulphur, the acid of chlorine Fampridine or the different monooctyl ester mixture of fluroxypyr conduct in-depth research, find ring sulphur ketone, thiophene ketone sulphur is grand, chlorine Fampridine sour or the different monooctyl ester mixture of fluroxypyr has Synergistic to respond, especially to Conyza canadensis (Conyzacanadensis), feather cockscomb, (Celosiaargentea), pivot stores (Polygonumaviculare) has obvious Synergistic to respond, and expands herbicide spectrum.Ring sulphur ketone, thiophene ketone sulphur are grand, chlorine Fampridine acid (or its ester type compound) composite without relevant report.
Summary of the invention
The object of the invention is to solve in prior art to farmland weed develop immunity to drugs problem and actual control efficiency poor, provide a kind of efficient, low toxicity, quick-acting are good and the lasting period is long, are conducive to the weed killer herbicide of the farmland weed comprehensive regulation.
Another object of the present invention is used for preventing and kill off corn field annual weed etc. by this weed killer herbicide.
Technical scheme: a kind of corn field herbicide, active ingredient is that ring sulphur ketone, thiophene ketone sulphur are grand, chlorine Fampridine acid (or its ester type compound); Ring sulphur ketone percentage by weight is in the composition 1% ~ 30%, the grand percentage by weight in the composition of thiophene ketone sulphur is 1% ~ 30%, chlorine Fampridine acid (or its ester type compound) percentage by weight is in the composition 1% ~ 40%, and all the other are insecticides adjuvant.
Described weed killer herbicide can add suitable insecticides adjuvant, according to well known to a person skilled in the art method, is processed into the application forms of the applicable agricultural uses such as oil-suspending agent, suspending agent, wetting powder or water dispersible granules.
The auxiliary agent used in weed killer herbicide of the present invention comprises solvent, emulsifier, wetting agent, stabilizing agent, dispersant, thickener, pH adjusting agent, defoamer, antifreezing agent, deionized water, filler etc., be all various auxiliary agents conventional in Pesticide formulation, concrete composition and consumption are determined by simple test according to recipe requirements.
The production technology of the various application forms of weed killer herbicide provided by the invention all belongs to existing known technology, does not repeat them here.
Weed killer herbicide provided by the invention, usually adopts and is watered the use of cauline leaf spray method, also can adopt other operation techniques agriculturally applied as required.
Weed killer herbicide provided by the invention, should use when applying before the corn field annual weed 5 leaf phase.
Weed killer herbicide provided by the invention has following beneficial effect:
1, weed killer herbicide provided by the invention, in certain ratio range, show obvious synergistic effect, control efficiency is significantly improved than single dose, reduce the using dosage of agricultural chemicals, decrease times for spraying, reduce drug cost, decrease the adverse effect of agricultural chemicals to ecotope.
2, weed killer herbicide provided by the invention, the combination of two kinds of effective ingredients, expands herbicidal spectrum, and a drug can solve various weed problem, compensate for defect when single dose uses and limitation.
3, weed killer herbicide provided by the invention, effective ingredient mechanism of action is different, can overcome the shortcoming that long-term single use easily produces resistance, extends the service life of medicament, to the comprehensive regulation important in inhibiting of Weed Resistance.
4, weed killer herbicide provided by the invention, drug effect plays rapidly, and the lasting period is long, and use cost is low, easy to use, time saving and energy saving, and it applies huge economic benefit and social benefit.
Embodiment
In order to make object of the present invention, technical scheme and advantage more short and sweet, the following specific embodiment of the present invention is described, but the present invention is only limitted to absolutely not these examples.The following stated is only the good embodiment of the present invention, only for describing the present invention, can not be interpreted as the restriction to scope of the present invention.It should be pointed out that all any amendments done within the spirit and principles in the present invention, equivalent replacement and improvement etc., all should be included within protection scope of the present invention.
Evaluate weed killer herbicide associated form (NY/T1155.7-2006) according to Colby method, its formula is as follows:
E 0 = A &times; B &times; C &times; ... N 100 ( n - 1 )
In formula:
A be ring sulphur ketone alone with certain dosage time fresh weight inhibition to target weeds;
B be thiophene ketone sulphur grand alone with certain dosage time fresh weight inhibition to target weeds;
C is the fresh weight inhibition to target weeds when chlorine Fampridine is sour or the different monooctyl ester of fluroxypyr is alone with certain dosage;
N is the weed killer herbicide kind number of mixture;
E 0for ring sulphur ketone, thiophene ketone sulphur are grand, the acid of chlorine Fampridine or fluroxypyr different monooctyl ester three kinds of pharmacy mix time theoretical value to target weeds fresh weight inhibition;
E is ring sulphur ketone, thiophene ketone sulphur is grand, the acid of chlorine Fampridine or fluroxypyr different monooctyl ester three kinds of pharmacy mix time be the measured value of contrast to target weeds fresh weight inhibition.
Evaluation criterion: work as E 0during ﹣ E > 10%, be expressed as synergistic function; As ﹣ 10%≤E 0during ﹣ E≤10%, show as collaborative summation action; Work as E 0during ﹣ E < ﹣ 10%, show as joint action of antagonism.
Embodiment one: ring sulphur ketone, thiophene ketone sulphur are grand, chlorine Fampridine acid and composite to Conyza canadensis (Conyzacanadensis), feather cockscomb (Celosiaargentea), pivot store (Polygonumaviculare) Toxicity Determination test.
Table 1, ring sulphur ketone, thiophene ketone sulphur are grand, chlorine Fampridine acid and composite to Conyza canadensis (Conyzacanadensis), Toxicity Determination result
Evaluate weed killer herbicide associated form according to Colby method, table 1 data show, and ring sulphur ketone, thiophene ketone sulphur are grand, chlorine Fampridine acid triple combination is remarkable to Conyza canadensis (Conyzacanadensis) synergistic effect, E 0-E value is all greater than 20%.
Table 2, ring sulphur ketone, thiophene ketone sulphur are grand, chlorine Fampridine sour and the composite Toxicity Determination result to feather cockscomb (Celosiaargentea)
Evaluate weed killer herbicide associated form according to Colby method, table 2 data show, ring sulphur ketone, thiophene ketone sulphur are grand, chlorine Fampridine acid triple combination to feather cockscomb (Celosiaargentea), E 0-E value is all greater than 20%.
Table 3, Dui pivot stores the Toxicity Determination result of (Polygonumaviculare)
Evaluate weed killer herbicide associated form according to Colby method, table 3 data show, and it is remarkable that ring sulphur ketone, thiophene ketone sulphur are grand, chlorine Fampridine acid triple combination Dui pivot stores (Polygonumaviculare) synergistic effect, E 0-E value is all greater than 20%.
Embodiment two: ring sulphur ketone, thiophene ketone sulphur are grand, the different monooctyl ester of fluroxypyr and composite to Conyza canadensis (Conyzacanadensis), feather cockscomb (Celosiaargentea), pivot store (Polygonumaviculare) Toxicity Determination test.
Table 4, Toxicity Determination result to Conyza canadensis (Conyzacanadensis)
Evaluate weed killer herbicide associated form according to Colby method, table 4 data show, and ring sulphur ketone, thiophene ketone sulphur are grand, the different monooctyl ester triple combination of fluroxypyr is remarkable to Conyza canadensis (Conyzacanadensis) synergistic effect, E 0-E value is all greater than 20%.
Table 5, Toxicity Determination result to feather cockscomb (Celosiaargentea)
Evaluate weed killer herbicide associated form according to Colby method, table 5 data show, ring sulphur ketone, thiophene ketone sulphur are grand, the different monooctyl ester triple combination of fluroxypyr to feather cockscomb (Celosiaargentea), E 0-E value is all greater than 20%.
Table 6, ring sulphur ketone, thiophene ketone sulphur are grand, the different monooctyl ester of fluroxypyr and composite Dui pivot thereof store the Toxicity Determination result of (Polygonumaviculare)
Evaluate weed killer herbicide associated form according to Colby method, table 6 data show, and it is remarkable that ring sulphur ketone, thiophene ketone sulphur are grand, fluroxypyr different monooctyl ester triple combination Dui pivot stores (Polygonumaviculare) synergistic effect, E 0-E value is all greater than 20%.
Embodiment three: ring sulphur ketone thiophene ketone sulphur grand chlorine Fampridine sour water dispersible granule.
Above-mentioned material is added in cone-type mixer together and mixes; pulverize by airslide disintegrating mill; material after pulverizing mixes through cone-type mixer again; mixed fineness of materials 98% is by 600 mesh standard sieves; add in kneader and be kneaded into plasticity material; finally this material is put into Squeezinggranulator extruder grain, after drying, screening, after granulation, namely obtain the ring sulphur ketone thiophene ketone sulphur grand chlorine Fampridine sour water dispersible granule of corresponding percentage by weight.
Embodiment four: ring sulphur ketone thiophene ketone sulphur grand chlorine Fampridine acid wetting powder.
Above-mentioned material is added in cone-type mixer together and mixes, pulverize by airslide disintegrating mill, material after pulverizing mixes through cone-type mixer again, mixed fineness of materials 98%, by 600 mesh standard sieves, obtains the ring sulphur ketone thiophene ketone sulphur grand chlorine Fampridine acid wetting powder of corresponding percentage by weight.
Embodiment five: ring sulphur ketone thiophene ketone sulphur grand chlorine Fampridine acid suspending agent.
Pulverized in advance in proportion by above-mentioned formula, then add in sand mill and grind, after high shear mixing, allotment obtains the ring sulphur ketone thiophene ketone sulphur grand chlorine Fampridine acid suspending agent of corresponding percentage by weight.
Embodiment six: ring sulphur ketone thiophene ketone sulphur grand chlorine Fampridine acid oil-suspending agent.
Above-mentioned material (except organobentonite) is joined in reactor mixer together, stir 2 hours, open pan feeding valve at the bottom of still, material is injected stage sand grinding machine to grind, fineness of materials 98% after grinding is by discharging after 1-5um, material puts into high-shear emulsifying still again together with the organobentonite dissolved in advance, namely can be made into the ring sulphur ketone thiophene ketone sulphur grand chlorine Fampridine acid oil-suspending agent of the good corresponding percentage by weight of flowing to property after emulsification.
Embodiment seven: the different monooctyl ester water dispersible granules of the grand fluroxypyr of ring sulphur ketone thiophene ketone sulphur.
Above-mentioned material is added in cone-type mixer together and mixes; pulverize by airslide disintegrating mill; material after pulverizing mixes through cone-type mixer again; mixed fineness of materials 98% is by 600 mesh standard sieves; add in kneader and be kneaded into plasticity material; finally this material is put into Squeezinggranulator extruder grain, after drying, screening, after granulation, namely obtain the different monooctyl ester water dispersible granules of the grand fluroxypyr of ring sulphur ketone thiophene ketone sulphur of corresponding percentage by weight.
Embodiment eight: the different monooctyl ester wetting powder of the grand fluroxypyr of ring sulphur ketone thiophene ketone sulphur.
Above-mentioned material is added in cone-type mixer together and mixes, pulverize by airslide disintegrating mill, material after pulverizing mixes through cone-type mixer again, mixed fineness of materials 98%, by 600 mesh standard sieves, obtains the different monooctyl ester wetting powder of the grand fluroxypyr of ring sulphur ketone thiophene ketone sulphur of corresponding percentage by weight.
Embodiment nine: the different monooctyl ester suspending agent of the grand fluroxypyr of ring sulphur ketone thiophene ketone sulphur.
Pulverized in advance in proportion by above-mentioned formula, then add in sand mill and grind, after high shear mixing, allotment obtains the different monooctyl ester suspending agent of the grand fluroxypyr of ring sulphur ketone thiophene ketone sulphur of corresponding percentage by weight.
Embodiment ten: the different monooctyl ester oil-suspending agent of the grand fluroxypyr of ring sulphur ketone thiophene ketone sulphur.
Above-mentioned material (except organobentonite) is joined in reactor mixer together, stir 2 hours, open pan feeding valve at the bottom of still, material is injected stage sand grinding machine to grind, fineness of materials 98% after grinding is by discharging after 1-5um, material puts into high-shear emulsifying still again together with the organobentonite dissolved in advance, namely can be made into the different monooctyl ester oil-suspending agent of the grand fluroxypyr of ring sulphur ketone thiophene ketone sulphur of the good corresponding percentage by weight of flowing to property after emulsification.
Embodiment 11: prevent and kill off corn field annual weed field control effectiveness test.
Table 7, prevent and kill off corn field annual weed field control effectiveness test result
In sum, instant component is reasonable, there is Synergistic response, expand herbicide spectrum, for corn field, especially with Conyza canadensis (Conyzacanadensis), feather cockscomb, (Celosiaargentea), pivot stores the corn field that (Polygonumaviculare) is advantage weeds and provides excellent weed control solution simultaneously.

Claims (3)

1. a corn field herbicide, is characterized in that: active ingredient is ring sulphur ketone, thiophene ketone sulphur is grand, chlorine Fampridine sour or its ester type compound; The percentage by weight of ring sulphur ketone in weed killer herbicide is 1% ~ 30%, and the grand percentage by weight in weed killer herbicide of thiophene ketone sulphur is 1% ~ 30%, chlorine Fampridine sour or the percentage by weight of its ester type compound in weed killer herbicide is 1% ~ 40%, and all the other are insecticides adjuvant.
2. corn field herbicide according to claim 1, is characterized in that: its formulation is the one in oil-suspending agent, suspending agent, wetting powder or water dispersible granules.
3. corn field herbicide according to claim 1 is preventing and kill off the application in corn field annual weed.
CN201510746490.4A 2015-11-04 2015-11-04 Corn field herbicide Pending CN105284853A (en)

Priority Applications (2)

Application Number Priority Date Filing Date Title
CN201510746490.4A CN105284853A (en) 2015-11-04 2015-11-04 Corn field herbicide
CN201610701058.8A CN106359428A (en) 2015-11-04 2016-08-22 Cornfield herbicide

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Application Number Priority Date Filing Date Title
CN201510746490.4A CN105284853A (en) 2015-11-04 2015-11-04 Corn field herbicide

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CN105284853A true CN105284853A (en) 2016-02-03

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CN201610701058.8A Pending CN106359428A (en) 2015-11-04 2016-08-22 Cornfield herbicide

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2023228176A1 (en) * 2022-05-23 2023-11-30 Adama Agan Ltd. Herbicidal composition comprising thiencarbazone and fluroxypyr

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Application publication date: 20160203