CN1316888C - Triflumuron mixed pesticide - Google Patents
Triflumuron mixed pesticide Download PDFInfo
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- CN1316888C CN1316888C CNB2004100169459A CN200410016945A CN1316888C CN 1316888 C CN1316888 C CN 1316888C CN B2004100169459 A CNB2004100169459 A CN B2004100169459A CN 200410016945 A CN200410016945 A CN 200410016945A CN 1316888 C CN1316888 C CN 1316888C
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- triflumuron
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- cypermethrin
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- 239000005942 Triflumuron Substances 0.000 title claims abstract description 40
- XAIPTRIXGHTTNT-UHFFFAOYSA-N triflumuron Chemical compound C1=CC(OC(F)(F)F)=CC=C1NC(=O)NC(=O)C1=CC=CC=C1Cl XAIPTRIXGHTTNT-UHFFFAOYSA-N 0.000 title claims abstract description 40
- 239000000575 pesticide Substances 0.000 title claims abstract description 35
- 229950001327 dichlorvos Drugs 0.000 claims abstract description 29
- OEBRKCOSUFCWJD-UHFFFAOYSA-N dichlorvos Chemical compound COP(=O)(OC)OC=C(Cl)Cl OEBRKCOSUFCWJD-UHFFFAOYSA-N 0.000 claims abstract description 27
- 150000001875 compounds Chemical class 0.000 claims description 15
- 241000238631 Hexapoda Species 0.000 abstract description 30
- 239000005946 Cypermethrin Substances 0.000 abstract description 2
- 241000255777 Lepidoptera Species 0.000 abstract description 2
- 229960005424 cypermethrin Drugs 0.000 abstract description 2
- 239000002131 composite material Substances 0.000 abstract 5
- 230000002349 favourable effect Effects 0.000 abstract 2
- KAATUXNTWXVJKI-UHFFFAOYSA-N cypermethrin Chemical compound CC1(C)C(C=C(Cl)Cl)C1C(=O)OC(C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 KAATUXNTWXVJKI-UHFFFAOYSA-N 0.000 abstract 1
- 230000000266 injurious effect Effects 0.000 abstract 1
- 230000002045 lasting effect Effects 0.000 abstract 1
- 230000002265 prevention Effects 0.000 abstract 1
- KAATUXNTWXVJKI-NSHGMRRFSA-N (1R)-cis-(alphaS)-cypermethrin Chemical compound CC1(C)[C@@H](C=C(Cl)Cl)[C@H]1C(=O)O[C@H](C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 KAATUXNTWXVJKI-NSHGMRRFSA-N 0.000 description 20
- 241000985245 Spodoptera litura Species 0.000 description 19
- 230000000694 effects Effects 0.000 description 11
- 239000003814 drug Substances 0.000 description 9
- 239000000126 substance Substances 0.000 description 7
- 229940079593 drug Drugs 0.000 description 6
- 239000004495 emulsifiable concentrate Substances 0.000 description 6
- 241000607479 Yersinia pestis Species 0.000 description 5
- -1 chlorfluron Chemical compound 0.000 description 5
- 238000009472 formulation Methods 0.000 description 5
- 239000000203 mixture Substances 0.000 description 5
- 239000003795 chemical substances by application Substances 0.000 description 4
- 239000002917 insecticide Substances 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 3
- KXDAEFPNCMNJSK-UHFFFAOYSA-N Benzamide Chemical compound NC(=O)C1=CC=CC=C1 KXDAEFPNCMNJSK-UHFFFAOYSA-N 0.000 description 2
- 241000257303 Hymenoptera Species 0.000 description 2
- 238000007598 dipping method Methods 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 230000005923 long-lasting effect Effects 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- 230000002688 persistence Effects 0.000 description 2
- 230000002195 synergetic effect Effects 0.000 description 2
- 231100000419 toxicity Toxicity 0.000 description 2
- 230000001988 toxicity Effects 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- AMVYOVYGIJXTQB-UHFFFAOYSA-N 3-[4-(4-methoxyphenoxy)phenyl]-1,1-dimethylurea Chemical compound C1=CC(OC)=CC=C1OC1=CC=C(NC(=O)N(C)C)C=C1 AMVYOVYGIJXTQB-UHFFFAOYSA-N 0.000 description 1
- 241000238876 Acari Species 0.000 description 1
- 241000251468 Actinopterygii Species 0.000 description 1
- 241000255789 Bombyx mori Species 0.000 description 1
- 239000005885 Buprofezin Substances 0.000 description 1
- 229920002101 Chitin Polymers 0.000 description 1
- 229940125842 Chitinase inhibitor Drugs 0.000 description 1
- 241000254173 Coleoptera Species 0.000 description 1
- 241000255925 Diptera Species 0.000 description 1
- 150000007945 N-acyl ureas Chemical class 0.000 description 1
- 241000238814 Orthoptera Species 0.000 description 1
- 231100000674 Phytotoxicity Toxicity 0.000 description 1
- 239000005937 Tebufenozide Substances 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
- 239000004480 active ingredient Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 239000012752 auxiliary agent Substances 0.000 description 1
- VEMKTZHHVJILDY-UXHICEINSA-N bioresmethrin Chemical compound CC1(C)[C@H](C=C(C)C)[C@H]1C(=O)OCC1=COC(CC=2C=CC=CC=2)=C1 VEMKTZHHVJILDY-UXHICEINSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- PRLVTUNWOQKEAI-VKAVYKQESA-N buprofezin Chemical compound O=C1N(C(C)C)\C(=N\C(C)(C)C)SCN1C1=CC=CC=C1 PRLVTUNWOQKEAI-VKAVYKQESA-N 0.000 description 1
- 150000004657 carbamic acid derivatives Chemical class 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 230000000856 effect on pests Effects 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- BNKAXGCRDYRABM-UHFFFAOYSA-N ethenyl dihydrogen phosphate Chemical compound OP(O)(=O)OC=C BNKAXGCRDYRABM-UHFFFAOYSA-N 0.000 description 1
- 230000037406 food intake Effects 0.000 description 1
- 235000012631 food intake Nutrition 0.000 description 1
- RGNPBRKPHBKNKX-UHFFFAOYSA-N hexaflumuron Chemical compound C1=C(Cl)C(OC(F)(F)C(F)F)=C(Cl)C=C1NC(=O)NC(=O)C1=C(F)C=CC=C1F RGNPBRKPHBKNKX-UHFFFAOYSA-N 0.000 description 1
- 230000000749 insecticidal effect Effects 0.000 description 1
- 238000004920 integrated pest control Methods 0.000 description 1
- 239000002949 juvenile hormone Substances 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 238000004806 packaging method and process Methods 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 231100000614 poison Toxicity 0.000 description 1
- 230000000607 poisoning effect Effects 0.000 description 1
- 230000007096 poisonous effect Effects 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 239000002728 pyrethroid Substances 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 210000002784 stomach Anatomy 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- QYPNKSZPJQQLRK-UHFFFAOYSA-N tebufenozide Chemical compound C1=CC(CC)=CC=C1C(=O)NN(C(C)(C)C)C(=O)C1=CC(C)=CC(C)=C1 QYPNKSZPJQQLRK-UHFFFAOYSA-N 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
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Abstract
Description
技术领域Technical field
本发明属于复配农药技术领域。The invention belongs to the technical field of compound pesticides.
背景技术 Background technique
昆虫生长调节剂目前已为世界众多国家研制和生产,成为第四代农药品种(如定虫隆、伏虫隆、氟铃脲、虫酰肼、杀铃脲、噻嗪酮等),均属于酰基脲类杀虫剂,对虫、螨具有触杀和胃毒作用。该类农药属几丁质酶抑制剂,抑制几丁质的形成,阻碍害虫正常蜕皮,使其变成畸形而死亡。对害虫活性较高,但作用速度较慢,幼虫接触药后不会很快死亡,但取食量明显减少,逐渐死亡。该农药对多种鳞翅目、直翅目、鞘翅目、膜翅目、双翅目等害虫具有很高的活性,是比较广谱的杀虫剂。对有机磷、氨基甲酸酯、拟除虫菊酯等杀虫剂产生抗药性的害虫有良好的防治效果。对天敌、蜜蜂、鱼等比较安全,对蚕有毒。在当前害虫综合防治中,尤其是无公害农产品的生产中是一类比较理想的杀虫剂。Insect growth regulators have been developed and produced for many countries in the world, and have become the fourth generation of pesticide varieties (such as difenoxuron, chlorfluron, hexaflumuron, tebufenozide, triflufluron, buprofezin, etc.), all of which belong to Acylurea insecticides have contact and stomach poisoning effects on insects and mites. This type of pesticide is a chitinase inhibitor, which inhibits the formation of chitin, hinders the normal molt of pests, and causes them to become deformed and die. It has high activity against pests, but the action speed is slow. The larvae will not die soon after contacting the medicine, but the food intake is obviously reduced and they die gradually. The pesticide has high activity against various Lepidoptera, Orthoptera, Coleoptera, Hymenoptera, Diptera and other pests, and is a relatively broad-spectrum insecticide. It has a good control effect on pests that are resistant to insecticides such as organophosphates, carbamates, and pyrethroids. It is relatively safe to natural enemies, bees, fish, etc., but poisonous to silkworms. It is an ideal insecticide in the current integrated pest control, especially in the production of pollution-free agricultural products.
鉴于这类农药速效性差,目前价位较高,如与目前我国取代高毒农药的一些中、低毒性的有机磷、菊酯类农药复配,将增加速效性、降低农药成本。In view of the poor quick-acting properties of this kind of pesticides, the current price is relatively high. If they are compounded with some medium and low-toxic organophosphorus and pyrethroid pesticides that replace highly toxic pesticides in my country, the quick-acting properties will be increased and the cost of pesticides will be reduced.
发明内容Contents of invention
基于上述问题,本发明目的在于提供一种杀虫谱较宽、成本较低、防治鳞翅目害虫效果好且速效性、持效性较好的杀铃脲复配农药的技术方案。Based on the above problems, the object of the present invention is to provide a technical solution of a compound pesticide of slumuron with a wide insecticidal spectrum, low cost, good effect in controlling lepidopteran pests, and good quick-acting and long-lasting effects.
所述的杀铃脲复配农药,其特征在于:含有杀铃脲0.3-10%,敌敌畏20-70%。The compound pesticide of triflumuron is characterized in that it contains 0.3-10% of triflumuron and 20-70% of dichlorvos.
所述的杀铃脲复配农药,其特征在于:杀铃脲的含量为0.5-5%,敌敌畏的含量为30-50%。The compound pesticide of triflumuron is characterized in that: the content of triflumuron is 0.5-5%, and the content of dichlorvos is 30-50%.
所述的杀铃脲复配农药,其特征在于:杀铃脲的含量为1-2%,敌敌畏的含量为40-50%。The compound pesticide of thiflumuron is characterized in that the content of thiflumuron is 1-2%, and the content of dichlorvos is 40-50%.
所述的杀铃脲复配农药,其特征在于:含有杀铃脲0.3-10%,高效氯氰菊酯0.5-5.0%%。The compound pesticide of triflumuron is characterized in that it contains 0.3-10% of triflumuron and 0.5-5.0% of beta-cypermethrin.
所述的杀铃脲复配农药,其特征在于:杀铃脲的含量为0.5-5%,高效氯氰菊酯的含量为1.5-5.0%。The compound pesticide of triflumuron is characterized in that: the content of flufluzuron is 0.5-5%, and the content of beta-cypermethrin is 1.5-5.0%.
所述的杀铃脲复配农药,其特征在于:杀铃脲的含量为1-2%,高效氯氰菊酯的含量为2.0-4.0%。The compound pesticide of triflumuron is characterized in that: the content of flufluzuron is 1-2%, and the content of beta-cypermethrin is 2.0-4.0%.
杀铃脲的化学名称为2-氯-N[[[4-(三氟甲氯基)苯基]氨基]羰基]苯甲酰胺;1-2(2-氯苯甲酰基)-3-(4三氟甲氧基苯基)脲;为已知物质,可以由吉林通化农药化工股份有限公司购得。The chemical name of slumuron is 2-chloro-N[[[4-(trifluoromethyl chloro)phenyl]amino]carbonyl]benzamide; 1-2(2-chlorobenzoyl)-3-( 4 trifluoromethoxyphenyl) urea; it is a known substance, which can be purchased by Jilin Tonghua Pesticide Chemical Co., Ltd.
敌敌畏的化学名称为0,0,-二甲基-0-(2.2.-二氯)乙烯基磷酸酯;为已知物质,可以由原上海农药厂购得。The chemical name of dichlorvos is 0,0,-dimethyl-0-(2.2.-dichloro)vinyl phosphate; it is a known substance and can be purchased from the former Shanghai Pesticide Factory.
高效氯氰菊酯的化学名称为(IR顺式)S及(IS顺式)R-α氰基-(3-苯氧苄基)-3-(2,2-二氯乙烯基)-2,2-二甲基环丙烷羰酸酯;为已知物质,可以用高效氯氰菊酯乳油,由原杭州农药厂购得。The chemical names of lambda-cypermethrin are (IR cis)S and (IS cis)R-αcyano-(3-phenoxybenzyl)-3-(2,2-dichlorovinyl)-2,2- Dimethylcyclopropane carboxylate; as a known substance, beta-cypermethrin EC can be purchased from the former Hangzhou Pesticide Factory.
所述的杀铃脲复配农药可制作成乳油,可由原药加入有机溶剂和乳化剂制得。具体复配生产工艺和常用助剂均属现有已知技术,在此不再赘述。当然,按已知技术,根据本技术方案也可以制成胶悬剂,即原药、有机溶剂或水,再加一系列助剂,经沙磨机研磨而成。The compound pesticide of slumuron can be made into emulsifiable concentrate, which can be prepared by adding organic solvent and emulsifier to the original drug. The specific compounding production process and commonly used additives belong to the existing known technology, and will not be repeated here. Certainly, according to the known technology, according to the technical proposal, it can also be made into a colloidal suspension, that is, the original drug, an organic solvent or water, plus a series of auxiliary agents, and then ground by a sand mill.
所述的杀铃脲复配农药,共毒系数达104-223,防治鳞翅目害虫效果好,防治率达98.0%,速效性和持效性较好,且使用成本低,仅为同类产品的1/3-1/2左右。The compound pesticide of slumuron has a co-toxicity coefficient of 104-223, is effective in preventing and controlling lepidopteran pests, and has a control rate of 98.0%, good quick-acting and long-lasting effects, and low use cost. About 1/3-1/2 of that.
本专利申请中的配比均为有效成分的纯物质的重量百分含量。The ratios in this patent application are all the weight percentages of the pure substances of active ingredients.
具体实施方式 Detailed ways
以下所述实施例详细说明了本发明。在这些实施例中,除另有说明外,所有百分比均为重量百分比。The examples described below illustrate the invention in detail. In these examples, all percentages are by weight unless otherwise indicated.
配方一:杀铃脲:0.5%,敌敌畏:49.5%。Formula 1: triflumuron: 0.5%, dichlorvos: 49.5%.
配方二:杀铃脲:1.0%,敌敌畏:49.0%。Formula 2: triflumuron: 1.0%, dichlorvos: 49.0%.
配方三:杀铃脲:1.5%,敌敌畏:48.5%。Formula 3: triflumuron: 1.5%, dichlorvos: 48.5%.
配方四:杀铃脲:2.0%,敌敌畏:48.0%。Formula 4: triflumuron: 2.0%, dichlorvos: 48.0%.
配方五:杀铃脲:2.5%,敌敌畏:47.5%。Formula five: triflumuron: 2.5%, dichlorvos: 47.5%.
配方六:杀铃脲:0.5%,高效氯氰菊酯:3.5%。Formula six: triflumuron: 0.5%, beta-cypermethrin: 3.5%.
配方七:杀铃脲:1.0%,高效氯氰菊酯:3.0%。Formula 7: triflumuron: 1.0%, beta-cypermethrin: 3.0%.
配方八:杀铃脲:1.5%,高效氯氰菊酯:2.5%。Recipe 8: triflumuron: 1.5%, beta-cypermethrin: 2.5%.
配方九:杀铃脲:2.0%,高效氯氰菊酯:2.0%。Formula 9: triflumuron: 2.0%, beta-cypermethrin: 2.0%.
配方十:杀铃脲:2.5%,高效氯氰菊酯:1.5%。Formula 10: triflumuron: 2.5%, beta-cypermethrin: 1.5%.
上述配方的复配农药及10%杀铃脲乳油、80%敌敌畏乳油、4.5%高效氯氰菊酯乳油对斜纹夜蛾进行对比试验,其共毒系数和药效试验数据如下:The compound pesticides of the above formula, 10% triflumuron EC, 80% dichlorvos EC, and 4.5% beta-cypermethrin EC were tested against Spodoptera litura, and the co-toxicity coefficient and efficacy test data are as follows:
50%杀铃脲·敌敌畏乳油对斜纹夜蛾共毒系数测定结果表
4%杀铃脲·高效氯氰菊酯乳油对斜纹夜蛾共毒系数测定结果表
10%杀铃脲乳油对斜纹夜蛾的药效试验
80%敌敌畏乳油对斜纹夜蛾的药效试验记录
4.5%高效氯氰菊酯乳油对斜纹夜蛾的药效试验记录
50%杀·敌乳油(配方一)对斜纹夜蛾的药效试验记录
50%杀·敌乳油(配方二)对斜纹夜蛾的药效试验记录
50%杀·敌乳油(配方三)对斜纹夜蛾的药效试验记录
50%杀·敌乳油(配方四)对斜纹夜蛾的药效试验记录
50%杀·敌乳油(配方五)对斜纹夜蛾的药效试验记录
4%杀·高乳油(配方六)对斜纹夜蛾的药效试验记录
4%杀·高乳油(配方七)对斜纹夜蛾的药效试验记录
4%杀·高乳油(配方八)对斜纹夜蛾的药效试验记录
4%杀·高乳油(配方九)对斜纹夜蛾的药效试验记录
4%杀·高乳油(配方十)对斜纹夜蛾的药效试验记录
50%杀铃脲·敌敌畏乳油(配方二)、4%杀铃脲·高效氯氰菊酯乳油(配方六)、10%杀铃脲乳油、80%敌敌畏乳油、4.5%高效氯氰菊酯乳油对斜纹夜蛾的田间药效试验数据如下:50% triflumuron·dichlorvos EC (formula two), 4% triflumezuron·beta-cypermethrin EC (formula six), 10% triflumezuron·dichlorvos EC, 80% dichlorvos EC, 4.5% beta-cypermethrin EC on the field of Spodoptera litura The efficacy test data are as follows:
杀铃脲与敌敌畏、高效氯氰菊酯复配剂防治斜纹夜蛾的效果表
采用饲料浸渍法,对斜纹夜蛾3龄幼虫的测定结果表明杀铃脲与敌敌畏的不同比例配方的共毒系数均大于100,都具有明显的增效作用。其中以50%杀铃脲·敌敌畏乳油(配方二)共毒系数最大,达146,从农药成本和药效角度考虑,50%杀铃脲·敌敌畏乳油(配方二)可作为优化方案选择。Using the feed dipping method, the test results on the 3rd instar larvae of Spodoptera litura showed that the co-toxicity coefficients of the formulations of different ratios of triflulumuron and dichlorvos were all greater than 100, and both had obvious synergistic effects. Among them, 50% trifluzuron·dichlorvos EC (Formulation 2) had the highest co-toxicity coefficient, reaching 146. Considering the cost and efficacy of pesticides, 50% Triflufluron·Dichlorvos EC (Formulation 2) could be selected as an optimal solution.
采用饲料浸渍法,对斜纹夜蛾3龄幼虫的测定结果表明杀铃脲与高效氯氰菊酯不同比例配方的共毒系数均大于100,都具有明显的增效作用。其中以4%杀铃脲·高效氯氰菊酯乳油(配方十)共毒系数最大,达223,,但其杀铃脲含量最高,成本较大;4%杀铃脲·高效氯氰菊酯乳油(配方六)共毒系数为168,但杀铃脲含量较低,持效期较短;从农药成本、药效、持效等多方面考虑4%杀铃脲·高效氯氰菊酯乳油(配方九)可作为优化方案选择。Using the feed dipping method, the test results on the third instar larvae of Spodoptera litura showed that the co-toxicity coefficients of different ratios of triflulumuron and beta-cypermethrin were all greater than 100, and both had obvious synergistic effects. Wherein with 4% triflumuron · beta-cypermethrin emulsifiable concentrate (prescription ten) co-toxicity coefficient is maximum, reaches 223, but its triflufluron content is the highest, and cost is bigger; The toxicity coefficient is 168, but the content of trifluzuron is low, and the persistence period is short; considering the cost of pesticides, drug efficacy, and persistence, 4% flufluzuron·beta-cypermethrin emulsifiable concentrate (formula 9) can be selected as an optimal solution .
从上述数据看出:50%杀铃脲·敌敌畏复配剂1000倍液(即每亩药量50ml),用药后3天防效达97.6%;7天的防效为96.8%;2000倍液(每亩药量25ml),3天防效为83.7%,7天防效为89%。1000倍液的速效与持效性均比两种对照药剂好。Find out from above-mentioned data: 1000 times of liquids of 50% triflumuron·dichlorvos compound agent (being 50ml per mu), the control effect reaches 97.6% in 3 days after medication; The control effect in 7 days is 96.8%; 2000 times of liquid (25ml of dosage per mu), the control effect in 3 days was 83.7%, and the control effect in 7 days was 89%. The quick-acting and sustained-acting properties of the 1000-fold solution were better than those of the two contrasting agents.
4%杀铃脲·高效氯氰菊酯复配剂1000倍液用药后3天防效为98%,7天后防效为97.3%;2000倍液3天后防效为87%,7天后防效为92.4%;均比两种对照药剂的防效好。The control effect of 1000 times liquid of 4% flufluzuron·beta-cypermethrin is 98% after 3 days and 97.3% after 7 days; the control effect of 2000 times liquid is 87% after 3 days and 92.4% after 7 days ; All are better than the control effect of two kinds of control agents.
上述药剂对试验作物未发生药害现象。The above-mentioned pesticides did not cause phytotoxicity to the experimental crops.
从生产成本上计算,50%杀铃脲·敌敌畏复配剂每吨农药成本为21000元,出厂价(包括包装费)为33000元左右。每亩用50ml计,每亩的农药成本费为1.8~2.0元左右。比单用10%杀铃脲乳油每亩50ml(4.0元左右)低一半。Calculated from the production cost, the pesticide cost per ton of 50% triflumuron·dichlorvos compound is 21,000 yuan, and the ex-factory price (including packaging fee) is about 33,000 yuan. Using 50ml per mu, the pesticide cost per mu is about 1.8-2.0 yuan. It is half lower than the 50ml per mu (about 4.0 yuan) of 10% triflumuron emulsifiable concentrate used alone.
4%杀铃脲·高效氯氰菊酯复配剂的成本价和出厂价与上述相近。The cost price and ex-factory price of 4% flufluzuron·beta-cypermethrin compound are similar to the above.
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