Embodiment
Following specific embodiments of the invention is elaborated.Should be understood that embodiment described herein only is used for explanation and explains the present invention, is not limited to the present invention.
On the one hand, the invention provides a kind of fosthiazate insecticides, composition contains active component and solvent, and active component contains the fosthiazate as main active, and fosthiazate accounts for the 20-100 weight % of active component total amount.
According to fosthiazate insecticides provided by the invention, although accounting for the 20-100 weight % of active component total amount, fosthiazate can realize the object of the invention, promptly improve control efficiency, under the preferable case, fosthiazate accounts for the 30-90 weight % of active component total amount; Further under the preferable case, fosthiazate accounts for the 50-60 weight % of active component total amount, can further improve the control efficiency of insecticides.
According to fosthiazate insecticides provided by the invention; Active component preferably also contains at least a systemic insecticide except that fosthiazate; The weight ratio of fosthiazate and at least a systemic insecticide except that fosthiazate is preferably 1: 0.12-2.3; More preferably 1: 0.67-1 under above-mentioned preferable case, can further improve the control efficiency of insecticides.
Among the present invention, at least a systemic insecticide except that fosthiazate can be preferably carbosulfan (carbosulfan for the conventional various systemic insecticides that use in this area; 2,3-dihydro-2,2-dimethyl benzofuran-7-base (dibutylamino sulphur)-N-methyl carbamate), Imidacloprid (imidacloprid; 1-(6-chloropyridine-6-pyridylmethyl)-N-Nitroimidazoline-2-base amine), Acetamiprid (acetaniprid, N-(N-cyanic acid-ethyleneimine base)-N-methyl-2-chloropyridine-5-methylamine), thiophene worm piperazine (thiamethoxam, 3-(2-chloro-1; 3-thiazole-5-ylmethyl)-the 5-methyl isophthalic acid, 3,5-oxadiazines-4-base fork (nitro) amine), Nitenpyram (nitenpyram; (E)-N-(6-chloro-3-picolyl)-N-ethyl-N '-methyl-2-nitro ethylene diamine), thiophene worm amine (clothianidin, (E)-1-(2-chloro-1,3-thiazoles-5-ylmethyl)-3-methyl-2-nitroguanidine), MTI-446 (dinotefuran; 1-methyl-2-nitro-3-(tetrahydrochysene-3-furfuryl) guanidine), imidaclothiz (imidaclothiz, 1-(5-chloro-2-thiazolyl methyl) N-Nitroimidazoline-2-base amine), Rynaxypyr (chlorantraniliprole, 3-bromo-N-[4-chloro-2-methyl-6-[(methyl-carbamoyl) benzene]-1-(3-chloropyridine-2-yl)-1-hydrogen-pyridine-5-formamide), Aphox (pirimicarb; 2-dimethylamino-5,6-dimethyl pyrimidine-4-base dimethylcarbamate), chlorophos (trichlorfon, 0; 0-dimethyl-(2,2,2-three-1-hydroxyethyl) phosphate), isazofos (isazofos; O-5-chloro-1-isopropyl-1H-1; 2,4-triazole-3-base-O, O-systox), pirimiphos-methyl (pirimiphos-methyl; O; O-dimethyl-O-(2-diethylin-6-methylpyrimidine-4-yl)-phosphorothionate), omethoate (omethoate, O, O-dimethyl-S-methyl (N-methylamino formyl methyl) thiophosphate), orthene (acephate; O; S-dimethyl acetyl group thio-phosphamide ester), thiophene worm quinoline (thiacloprid, (Z)-3-(6-chloro-3-picoline)-1,3-thiazoles alkane-the inferior cyanamide of 2-), butyl pyrimidine phosphorus (tebupirimfos; O-(2-tert-butyl group pyrimidine-5-yl)-O-ethyl-O-isopropyl phosphorothionate), fluorine worm nitrile (fipronil; (RS)-5-amino-1-(2,6-dichlor-4-trifluoromethyl phenyl)-4-trifluoromethyl sulfinyl pyrazole-3-nitrile), capillary (chlorfenapyr, 4-bromo-2-(4-chlorphenyl)-1-ethoxyl methyl-5-trifluoromethyl pyrpole-3-nitrile), pyrrole aphid ketone (pymetrozine; (E)-4; 5-dihydro-6-methyl-4-(3-pyridine methylene amino)-1,2,4-triazine-3 (2H)-ketone) at least a in.
Inventor of the present invention is surprised to find that; When at least a systemic insecticide except that fosthiazate is at least a in Imidacloprid, Acetamiprid, thiophene worm piperazine, Rynaxypyr and the thiophene worm quinoline; Be at least a composite use in fosthiazate and Imidacloprid, Acetamiprid, thiophene worm piperazine, Rynaxypyr and the thiophene worm quinoline during as the active component of insecticides, the control efficiency of fosthiazate insecticides provided by the invention obviously improves.Therefore, the further preferred at least a systemic insecticide except that fosthiazate of the present invention is at least a in Imidacloprid, Acetamiprid, thiophene worm piperazine, Rynaxypyr and the thiophene worm quinoline.
Fosthiazate insecticides provided by the invention does not have specific (special) requirements for the content of solvent, can adopt the conventional solvent that uses in this area, is that 100 weight portions are benchmark with active component, and under the preferable case, solvent is the 10-100000 weight portion; Further under the preferable case, solvent is the 100-10000 weight portion; Further under the preferable case, solvent is the 500-1000 weight portion.There is not specific (special) requirements for solvent types yet; The conventional solvent that uses in this area can be adopted, for example in methyl alcohol, ethanol, propyl alcohol, isopropyl alcohol, propane diols, glycerine, n-butanol, isobutanol, the tert-butyl alcohol, n-amyl alcohol, isoamyl alcohol, n-hexyl alcohol, n-heptanol, n-octyl alcohol, ethylene glycol, glycol monoethyl ether, glycol dimethyl ether, sorbierite and the aromatic hydrocarbon solvent oil one or more can be.
Because fosthiazate insecticides provided by the invention is a systemic insecticide; Therefore; It will be understood by those skilled in the art that fosthiazate insecticides provided by the invention preferably adopts the mode that is expelled in the recipient plant body to use in order to improve the effective rate of utilization of insecticide.The position of corroding for the injection site that makes recipient plant and by insect can very fast healing, and fosthiazate insecticides provided by the invention preferably also contains Wound-healing agent.In order to give full play to the wound healing function of Wound-healing agent, can also fully guarantee the insecticidal action of active component, be that 100 weight portions are benchmark with active component, Wound-healing agent is preferably the 20-200 weight portion.Kind for Wound-healing agent does not have specific (special) requirements; The conventional various Wound-healing agents that use in this area can be adopted, for example in humus, glucose, acetyl shitosan, methyl, Fluoxastrobin, albendazole, carbendazim, thiophanate-methyl, carboxin, benomyl, tmtd, production increasing agent, indolebutyric acid and the brassin lactones one or more can be.
For stability and the biologically active that improves fosthiazate insecticides provided by the invention, fosthiazate insecticides provided by the invention preferably also contains emulsifier.For the content of emulsifier, be that 100 weight portions are benchmark with active component, emulsifier is preferably the 10-500 weight portion, further is preferably the 30-150 weight portion.There is not specific (special) requirements for emulsifier type; The conventional various emulsifier that use in this area can be adopted, for example in calcium dodecyl benzene sulfonate, succinate sodium sulfonate, styryl phenol polyethenoxy ether phosphate, benzylphenol polyoxyethylene ether phosphate, sorbitan trioleate, anhydrous sorbitol tristearate, polyoxyethylene sorb ether alcohol six stearates, cithrol, polyoxyethylene sorbitol ether beeswax derivative, polyethylene glycol mono stearate, sorbitan sesquioleate, glyceryl monostearate, sorbitan monooleate, sorbitan monostearate, dibenzyl phenol polyethenoxy ether, diethylene glycol fatty acid ester, diethylene glycol monolaurate, sorbitan mono-laurate, Brij30, polyoxyethylene monopalmitate, APES, Brij30, anhydrous sorbitol APEO, polyoxyethylene sorbitan ether monoleate, styryl phenol polyethenoxy ether, AEO, aliphatic amine polyoxyethylene ether and the castor oil polyoxyethylene ether one or more can be.
For absorbability and the conductivity that improves fosthiazate insecticides provided by the invention, and then improve quick-acting, fosthiazate insecticides provided by the invention preferably also contains bleeding agent.For the content of bleeding agent, be that 100 weight portions are benchmark with active component, bleeding agent is preferably the 1-100 weight portion, further is preferably the 10-50 weight portion.Kind for bleeding agent does not have specific (special) requirements; The conventional various bleeding agents that use in this area can be adopted, for example azone, thiophene ketone, AEO, polyoxyalkylene modification polymethyl siloxane, dimethicone one or more in polyol, sulfosuccinate di-isooctyl sodium salt and the castor oil sodium sulfonate altogether can be.
In order to prolong the lasting period of fosthiazate insecticides provided by the invention, fosthiazate insecticides provided by the invention preferably also contains controlled release agent.For the content of controlled release agent, be that 100 weight portions are benchmark with active component, controlled release agent is preferably the 10-100 weight portion.Kind for controlled release agent does not have specific (special) requirements; The conventional various controlled release agent of using in this area can be adopted, for example in n-hexane, cyclohexane, n-dodecane, methyl oleate, ethyl oleate, butyl oleate, ethyl acetate, repefral, diethyl phthalate, dibutyl phthalate, polyethylene glycol and the polyvinyl alcohol one or more can be.
The preparation method of fosthiazate insecticides provided by the invention is simple; As long as above-mentioned various components are mixed in proportion; To the hybrid mode and the not special qualification of order by merging of various compositions, this area various hybrid modes commonly used all can realize the object of the invention.
The method for using of fosthiazate insecticides provided by the invention is simple; Can this fosthiazate insecticides directly be used as insecticide; Also can dilute the back uses as insecticide; Also can unite use, be used for preventing and treating the various pests of forest, gardens, fruit-bearing forest with other insecticide or bactericide.In active component, the dosage that uses is the 0.1-10g/ strain, and concrete dosage can be confirmed according to the kind of recipient plant, size etc.
When fosthiazate insecticides provided by the invention uses as insecticide; Can adopt the conventional variety of way in this area to use, for example can the present composition be sprayed at plant surface, also can be injected in the plant corpus; Because fosthiazate insecticides provided by the invention is a systemic insecticide; Therefore, in order to improve the medicament effective rate of utilization, preferably fosthiazate insecticides provided by the invention is injected in the plant corpus.
When injection is used, be preferable on the trunk and become the oblique punching down of miter angle with the trunk main shaft.Punch position can be more than butt 30cm, below branch; Confirm punching quantity according to the plant corpus size.When said hole when being a plurality of, preferred a plurality of holes evenly distribute around the trunk, and stagger up and down, avoid sustained height that 2 holes are arranged.The punching degree of depth is grasped at 5-12cm according to the plant corpus size.The punching less, hole depth, help the soup fast Absorption, action effect is rapid.After punching finished, the liquor that fosthiazate insecticides provided by the invention is made into was expelled in the plant corpus through the hole.Be typically about 2 hours inject time, fills in the cork filler opening after injection finishes.
On the other hand, the invention provides the application of aforesaid composition in preparation injection liquid insecticides.
More than describe preferred implementation of the present invention in detail; But the present invention is not limited to the detail in the above-mentioned embodiment, in technical conceive scope of the present invention; Can carry out multiple simple variant to technical scheme of the present invention, these simple variant all belong to protection scope of the present invention.
Need to prove in addition; Each concrete technical characterictic described in above-mentioned embodiment under reconcilable situation, can make up through any suitable manner; For fear of unnecessary repetition, the present invention is to the explanation no longer separately of various possible compound modes.
In addition, also can carry out combination in any between the various embodiment of the present invention, as long as it is without prejudice to thought of the present invention, it should be regarded as the disclosed content of the present invention equally.
Embodiment
Following embodiment will be further described the present invention, but therefore not limit the present invention.
In following embodiment and Comparative Examples:
The anhydrous sorbitol APEO is purchased the outstanding chemical industry Co., Ltd in sea, Zibo, model T-60;
Isomery ten pure APEOs are purchased the literary composition sunshine chemical industry Co., Ltd in Nantong, model E-05.
Embodiment 1
This embodiment is used to explain the preparation of fosthiazate insecticides provided by the invention.
Fosthiazate, thiophene worm quinoline, anhydrous sorbitol APEO, thiophene ketone, n-hexane, humus, glycol monoethyl ether and ethanol is even according to following mixed, and obtain forming following fosthiazate insecticides: fosthiazate is 55 weight portions, and thiophene worm quinoline is 45 weight portions; The anhydrous sorbitol APEO is 80 weight portions; Thiophene ketone is 10 weight portions, and n-hexane is 50 weight portions, and humus is 20 weight portions; Glycol monoethyl ether is 280 weight portions, and ethanol is 660 weight portions.
Embodiment 2
This embodiment is used to explain the preparation of fosthiazate insecticides provided by the invention.
Fosthiazate, Acetamiprid, calcium dodecyl benzene sulfonate, isomery ten pure APEOs, butyl oleate, Fluoxastrobin and isopropyl alcohol is even according to following mixed; Obtain forming following fosthiazate insecticides: fosthiazate is 60 weight portions, and Acetamiprid is 40 weight portions, and calcium dodecyl benzene sulfonate is 100 weight portions; Isomery ten pure APEOs are 20 weight portions; Butyl oleate is 80 weight portions, and Fluoxastrobin is 70 weight portions, and isopropyl alcohol is 610 weight portions.
Embodiment 3
This embodiment is used to explain the preparation of fosthiazate insecticides provided by the invention.
Fosthiazate, thiophene worm piperazine, sorbitan trioleate, azone, methyl oleate, carbendazim, glycol dimethyl ether and n-butanol is even according to following mixed, and obtain forming following fosthiazate insecticides: fosthiazate is 55 weight portions, and thiophene worm piperazine is 45 weight portions; Sorbitan trioleate is 100 weight portions; Azone is 10 weight portions, and methyl oleate is 100 weight portions, and carbendazim is 200 weight portions; Glycol dimethyl ether is 210 weight portions, and n-butanol is 290 weight portions.
Embodiment 4
This embodiment is used to explain the preparation of fosthiazate insecticides provided by the invention.
Fosthiazate, Imidacloprid, glyceryl monostearate, castor oil sodium sulfonate, repefral, tmtd and n-hexyl alcohol is even according to following mixed; Obtain forming following fosthiazate insecticides: fosthiazate is 50 weight portions, and Imidacloprid is 50 weight portions, and glyceryl monostearate is 150 weight portions; The castor oil sodium sulfonate is 10 weight portions; Repefral is 100 weight portions, and tmtd is 150 weight portions, and n-hexyl alcohol is 690 weight portions.
Embodiment 5
This embodiment is used to explain the preparation of fosthiazate insecticides provided by the invention.
Fosthiazate, Rynaxypyr, sorbitan monostearate, castor oil sodium sulfonate, cyclohexane, sorbierite and glycerine is even according to following mixed; Obtain forming following fosthiazate insecticides: fosthiazate is 55 weight portions, and Rynaxypyr is 45 weight portions, and sorbitan monostearate is 50 weight portions; The castor oil sodium sulfonate is 30 weight portions; Cyclohexane is 10 weight portions, and sorbierite is 600 weight portions, and glycerine is 300 weight portions.
Embodiment 6
This embodiment is used to explain the preparation of fosthiazate insecticides provided by the invention.
Fosthiazate, thiophene worm piperazine, Rynaxypyr, diethylene glycol monolaurate, sulfosuccinate di-isooctyl sodium salt, n-dodecane, methyl, ethylene glycol and propane diols is even according to following mixed; Obtain forming following fosthiazate insecticides: fosthiazate is 50 weight portions; Thiophene worm piperazine is 40 weight portions, and Rynaxypyr is 10 weight portions, and the diethylene glycol monolaurate is 30 weight portions; Sulfosuccinate di-isooctyl sodium salt is 50 weight portions; N-dodecane is 100 weight portions, and methyl is 100 weight portions, and ethylene glycol is that 670 weight portions and propane diols are 30 weight portions.
Embodiment 7
This embodiment is used to explain the preparation of fosthiazate insecticides provided by the invention.
Method according to embodiment 1 prepares the fosthiazate insecticides, and different is, fosthiazate is 70 weight portions, and thiophene worm quinoline is 30 weight portions, and all the other ingredients weight parts are constant.
Embodiment 8
This embodiment is used to explain the preparation of fosthiazate insecticides provided by the invention.
Method according to embodiment 1 prepares the fosthiazate insecticides, and different is, fosthiazate is 40 weight portions, and thiophene worm quinoline is 60 weight portions, and all the other ingredients weight parts are constant.
Embodiment 9
This embodiment is used to explain the preparation of fosthiazate insecticides provided by the invention.
Method according to embodiment 1 prepares the fosthiazate insecticides, and different is that thiophene worm quinoline is replaced with Nitenpyram.
Embodiment 10
This embodiment is used to explain the preparation of fosthiazate insecticides provided by the invention.
Method according to embodiment 1 prepares the fosthiazate insecticides, and different is, does not contain thiophene worm quinoline, and fosthiazate is 100 weight portions, and all the other ingredients weight parts are constant.
Comparative Examples 1
Method according to embodiment 1 prepares the fosthiazate insecticides, and different is, this fosthiazate insecticides does not contain fosthiazate, and thiophene worm quinoline is 100 weight portions, and all the other ingredients weight parts are constant.
Comparative Examples 2
Method according to embodiment 1 prepares the fosthiazate insecticides, and different is, fosthiazate is 10 weight portions, and thiophene worm quinoline is 90 weight portions, and all the other ingredients weight parts are constant.
Test case
In following each test case, lethality is measured through following method.
Lethality: choose the roughly the same target pest of size; Be positioned over the selected in advance good no worm trees of growth conditions dispersedly; Every strain trees are placed 50 heads and mark insect; The mode of injecting through punching then is to the tree injection insecticides, then respectively in the dead quantity of 24h, 48h and 72h record object insect.A kind of insecticides of every strain tree injection, every kind of insecticides carries out 5 groups of repetitions, and by formula (I) calculated the lethality that each is handled, and unit is percentage (%).
P
1=K/N×100 (Ⅰ)
In the formula (I): P
1-lethality, the dead borer population of K-, N-handles total borer population.
Test case 1
Selecting the diameter of a cross-section of a tree trunk 1.3 meters above the ground for use is that the masson pine of 19-21cm is some, and according to the method injection embodiment 1-10 of said determination lethality and the insecticides of Comparative Examples 1-2,60ml is injected in every strain.Each insecticides is as shown in table 1 to the control efficiency (lethality with Monochamus alternatus Hope, pine caterpillars is represented) of masson pine Monochamus alternatus Hope, pine caterpillars.
Table 1
Test case 2
Selecting the diameter of a cross-section of a tree trunk 1.3 meters above the ground for use is that the apple tree of 19-21cm is some, and according to the method injection embodiment 1-10 of said determination lethality and the insecticides of Comparative Examples 1-2,60ml is injected in every strain.Each insecticides is as shown in table 2 to the control efficiency (lethality with codling moth, thrips is represented) of codling moth, thrips.
Table 2
Test case 3
Selecting the diameter of a cross-section of a tree trunk 1.3 meters above the ground for use is that the Chinese white poplar of 19-21cm is some, and according to the method injection embodiment 1-10 of said determination lethality and the insecticides of Comparative Examples 1-2,60ml is injected in every strain.Each insecticides is as shown in table 3 to the control efficiency (lethality with Monochamus alternatus Hope, scale insect is represented) of Monochamus alternatus Hope, scale insect.
Table 3
Test case 4
Selecting the diameter of a cross-section of a tree trunk 1.3 meters above the ground for use is that the ginkgo of 19-21cm is some, and according to the method injection embodiment 1-10 of said determination lethality and the insecticides of Comparative Examples 1-2,60ml is injected in every strain.Each insecticides is as shown in table 4 to the control efficiency (lethality with scale insect, African mole cricket is represented) of scale insect, African mole cricket.
Table 4
The result who shows the embodiment 1-10 among the 1-4 is compared with the result of Comparative Examples 1, can find out and contain fosthiazate in the insecticides, can improve the control efficiency of insecticides greatly; The result who shows the embodiment 1-10 among the 1-4 is compared with the result of Comparative Examples 2, can find out that fosthiazate accounts for the 20-100 weight % of active component total amount, can improve the control efficiency of insecticides greatly.
The result of embodiment 1 among the table 1-4 is compared with the result of embodiment 8 with embodiment 7 respectively, can find out that fosthiazate accounts for the 50-60 weight % of active component total amount, can improve the control efficiency of insecticides better; The result who shows the embodiment 1 among the 1-4 is compared with the result of embodiment 9; Can find out that at least a systemic insecticide except that fosthiazate is at least a in Imidacloprid, Acetamiprid, thiophene worm piperazine, Rynaxypyr and the thiophene worm quinoline, can improve the control efficiency of insecticides better; The result who shows the embodiment 1 among the 1-4 is compared with the result of embodiment 10; Can find out that fosthiazate is composite as active component with at least a systemic insecticide except that fosthiazate; Than using fosthiazate separately, more help improving the control efficiency of insecticides as active component.
Fosthiazate insecticides provided by the invention, interior suction conductivity is strong, and target is strong; Effect rapidly; To longicorn, pine wood nematode, scale insect, armored scale, root-knot nematode etc. live in inside the trunk or underground pest controling effect good, when injection was used, the lethality of insect can reach more than 90%; Not dilute with water, therefore preparation and easy to use in preparation and the use; When injection was used, the medicament effective rate of utilization was high.Adopt optimal way of the present invention, fosthiazate and the composite use of other systemic insecticides have synergistic effect, have not only improved insecticidal activity, and have enlarged the desinsection scope; Delayed drug-fast development; Reduced the consumption of every kind of systemic insecticide, reduced influence environment, safer to people and animals.Fosthiazate insecticides provided by the invention can be widely used in agriculture and forestry desinsection fields such as forest, gardens, fruit tree.