CN1131670C - 杀真菌活性化合物组合物 - Google Patents
杀真菌活性化合物组合物 Download PDFInfo
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- CN1131670C CN1131670C CN00127076A CN00127076A CN1131670C CN 1131670 C CN1131670 C CN 1131670C CN 00127076 A CN00127076 A CN 00127076A CN 00127076 A CN00127076 A CN 00127076A CN 1131670 C CN1131670 C CN 1131670C
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Classifications
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- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION 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
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/18—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing the group —CO—N<, e.g. carboxylic acid amides or imides; Thio analogues thereof
- A01N37/22—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing the group —CO—N<, e.g. carboxylic acid amides or imides; Thio analogues thereof the nitrogen atom being directly attached to an aromatic ring system, e.g. anilides
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION 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
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/18—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing the group —CO—N<, e.g. carboxylic acid amides or imides; Thio analogues thereof
- A01N37/22—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing the group —CO—N<, e.g. carboxylic acid amides or imides; Thio analogues thereof the nitrogen atom being directly attached to an aromatic ring system, e.g. anilides
- A01N37/24—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing the group —CO—N<, e.g. carboxylic acid amides or imides; Thio analogues thereof the nitrogen atom being directly attached to an aromatic ring system, e.g. anilides containing at least one oxygen or sulfur atom being directly attached to the same aromatic ring system
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Wood Science & Technology (AREA)
- General Health & Medical Sciences (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Zoology (AREA)
- Dentistry (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (AREA)
- Engineering & Computer Science (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Pyridine Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Indole Compounds (AREA)
- Heterocyclic Compounds Containing Sulfur Atoms (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
本发明叙述了式(I)化合物与已知的杀真菌活性化合物组成的新的活性化合物组合物,以及它们在防治植物致病真菌方面的用途。
Description
本申请是1994年4月28日提交的、题为“杀真菌活性化合物组合物”的94104652.4号发明专利申请的分案申请。
技术领域
背景技术
已知式(I)化合物具有杀真菌的作用(参见EP-A 339,418)。该物质的活性是高的,但是在某些情况下,在其低的施药剂量下,有些方面还有待于改进。
还已知许多氮杂茂环衍生物、芳香族羧酸衍生物、吗啉类化合物和其它杂环类化合物可以用于防治真菌(参见K.H.Büchel:“Pflanzenschutz und Schdlingsbekampfung”[植物保护和农业病虫害防治],p87,136,140,141和146~153,Georg Thieme Verlag,Stuttgart 1977)。
但是,在低的施药剂量下,有关物质的作用未必总是令人满意的。
发明内容
现已发现,式I化合物与下述化合物组成的新的活性化合物组合物具有非常好的杀真菌作用:
(E)二硫化四甲基秋兰姆(福美双)(式VI),和/或
(G)敌菌灵(式VII),和/或
(H)王铜和/或
(N)霜脲氰(式XII),和/或
(O)苯并咪唑-2-氨基甲酸甲基酯(多菌灵)(式XIII),和/或
(Q)甲霜灵(式XV)和/或
(T)1-(4-氯苯基)-4,4-二甲基-3-(1,2,4-三唑-1-基-乙基)-戊-3-醇(戊醇唑)(式XVIII),和/或
(V)选自以下一组的氮杂茂环衍生物:
a)恶醚唑
b)戊菌唑
c)氟硅唑(flusilazole)
d)己唑醇(hexaconazole)
e)腈菌唑(myclobutanil)
f)扑菌唑(prochloraz)和/或
(W)代森联和/或
(X)密霉胺和/或
(Y)乙霉威(diethofencarb)和/或
(Z)嘧菌胺和/或
(α)苯基吡咯和/或
(β)异菌脲和/或
(γ)乙烯菌核利和/或
(δ)速克灵和/或
(ε)苯来特和/或
(ω)甲基托布津和/或
(π)硫磺和/或
(η)下式化合物
式(I)活性化合物是已知的(EP-A-339,418)。存在于本发明组合物中的其它成分也是已知的。
除了式(I)活性化合物之外,本发明的活性化合物组合物含有至少一种选自化合物(A)至(π)的活性化合物,而且本发明的活性化合物组合物还可以含有其它的杀真菌活性混用成分
如果活性化合物以一定重量比例存在于本发明活性化合物组合物中,则显示出特别明显的增效作用。但是,活性化合物在活性化合物组合物中的重量比例可以在较宽的范围内变化。一般来讲,下面的比例是按1份重量的式(I)活性化合物来确定的:0.5~50份(按重量计),优选0.5~10份(按重量计) 活性化合物甲基代森锌(D)0.5~50份(按重量计),优选0.5~10份(按重量计) 活性化合物代森锰(F)0.5~50份(按重量计),优选0.5~10份(按重量计) 活性化合物福美双(E)0.5~50份(按重量计),优选0.5~10份(按重量计) 活性化合物代森联(W)0.5~50份(按重量计),优选0.5~20份(按重量计) 活性化合物抑菌灵(A)0.5~50份(按重量计),优选0.5~20份(按重量计) 活性化合物对甲抑菌灵(B)0.5~50份(按重量计),优选0.5~20份(按重量计) 活性化合物灭菌丹(M)0.5~50份(按重量计),优选0.5~20份(按重量计) 活性化合物克菌丹(I)1~50份(按重量计),优选1~20份(按重量计) 活性化合物王铜(H)1~50份(按重量计),优选1~20份(按重量计) 活性化合物流磺(π)0.5~50份(按重量计),优选0.5~10份(按重量计) 活性化合物敌菌灵(G)0.5~50份(按重量计),优选0.5~10份(按重量计) 活性化合物百菌清(C)0.5~50份(按重量计),优选0.5~10份(按重量计) 活性化合物二噻农(L)0.1~10份(按重量计),优选0.5~5份(按重量计) 活性化合物氟啶胺(S)0.1~10份(按重量计),优选0.5~5份(按重量计) 活性化合物密霉胺 (X)0.1~10份(按重量计),优选0.5~5份(按重量计) 活性化合物乙霉威(Y)0.1~10份(按重量计),优选0.5~5份(按重量计) 活性化合物嘧菌胺 (Z)0.1~10份(按重量计),优选0.5~5份(按重量计) 活性化合物苯基吡咯(Saphire)(α)0.1~20份(按重量计),优选0.5~10份(按重量计) 活性化合物异菌脲(β)0.1~20份(按重量计),优选0.5~10份(按重量计) 活性化合物乙烯菌核利(γ)0.1~20份(按重量计),优选0.5~10份(按重量计) 活性化合物速克灵(δ)0.1~10份(按重量计),优选0.25~5份(按重量计) 活性化合物苯来特(ε)0.1~10份(按重量计),优选0.25~5份(按重量计) 活性化合物多菌灵(O)0.1~10份(按重量计),优选0.25~5份(按重量计) 活性化合物甲基托布津(ω)0.1~10份(按重量计),优选0.25~5份(按重量计) 活性化合物霜脲氰(N)0.1~10份(按重量计),优选0.25~5份(按重量计) 活性化合物甲霜灵(Q)0.1~10份(按重量计), 优选0.25~5份(按重量计) 活性化合物恶霜灵(R)0.1~10份(按重量计), 优选0.2~5份(按重量计) 活性化合物烯酰吗啉 (K)0.1~20份(按重量计), 优选0.2~10份(按重量计) 活性化合物乙膦铝(P)0.01~10份(按重量计),优选0.025~5份(按重量计) 活性化合物戊醇唑 (T)0.01~10份(按重量计),优选0.025~5份(按重量计) 活性化合物三唑酮(U XIXc)0.01~10份(按重量计),优选0.025~5份(按重量计) 活性化合物三唑醇(U XIXa)0.01~10份(按重量计),优选0.025~5份(按重量计) 活性化合物双苯三唑醇(U XIXb)0.01~10份(按重量计),优选0.025~5份(按重量计) 活性化合物恶醚唑 (Va)0.01~10份(按重量计),优选0.025~5份(按重量计) 活性化合物戊菌唑 (Vb)0.01~10份(按重量计),优选0.025~5份(按重量计) 活性化合物氟硅唑(Vc)0.01~10份(按重量计),优选0.025~5份(按重量计) 活性化合物己唑醇(Vd)0.01~10份(按重量计),优选0.025~5份(按重量计) 活性化合物腈菌唑(Ve)0.01~10份(按重量计),优选0.025~5份(按重量计) 活性化合物扑菌唑(Vf)0.01~10份(按重量计),优选0.025~5份(按重量计) 活性化合物式(ηa)0.01~10份(按重量计),优选0.025~5份(按重量计) 活性化合物式(ηb)
本发明的活性化合物组合物具有非常好的杀真菌的作用,并且尤其可用于防治植物致病真菌,例如根肿粘菌、卵菌、壶菌、接合菌、子囊菌、担子菌、半知菌等。
本发明的活性化合物组合物尤其适用于防治禾谷类病害,例如白粉菌、旋孢腔菌、核腔菌和小球腔菌,以及适用于抗真菌对蔬菜、葡萄和水果的侵害,例如抗苹果黑星菌、抗豆葡萄孢和抗番茄疫霉。
在防治植物病害必需的浓度下,活性化合物组合物良好的植物耐受性使处理植物的地上部分、处理植物、种子和土壤成为可能。
可以将本发明的活性化合物组合物制备成常用的剂型,例如溶液剂、乳剂、悬浮剂、粉剂、泡沫剂、糊剂、粒剂、气雾剂、在聚合物质中的微囊剂、种子包衣组合物以及超低容量喷雾剂。
所述制剂可按已知的方法进行制备,例如将活性化合物或活性化合物组合物与增容剂,即液体溶剂、在压力下的液化气体,和/或固体载体;可任选应用表面活性剂,即乳化剂和/或分散剂和/或生泡剂;一起混合。在应用水作为增容剂的情况下,也可以应用有机溶剂作为辅助溶剂。作为液体溶剂,适用的主要有:芳香族化合物,如二甲苯、甲苯或烷基萘;氯代芳香族化合物或氯代脂肪族烃,如氯苯、二氯乙烯或二氯甲烷;脂肪族烃,如环己烷或烷属烃(如矿物油馏分);醇类,如丁醇或甘醇;及其醚、酯和酮,如丙酮、甲基乙基酮、甲基异丁基酮或环己酮;强极性溶剂,如二甲基甲酰胺和二甲基亚砜及水。液化的气体增容剂或载体是指在大气压力和环境温度下为气态的液体,例如气溶胶推进剂如卤代烃以及丁烷、丙烷、氮和二氧化碳。作为固体载体适用的有:例如粉碎的天然矿物如高岭土、粘土、滑石、白垩、石英、绿坡缕石、蒙脱土或硅藻土;粉碎的人工矿物如高分散性二氧化硅、氧化铝和硅酸盐。适用于粒剂的固体载体有;例如粉碎和分级的天然矿物如方解石、大理石、浮石、海泡石和白云石,以及合成的无机颗粒和有机的粗磨谷粉,和有机物质的颗粒如锯末、椰子壳、玉米穗轴和烟草茎。适于作为乳化剂和/或生泡剂 用的有:例如非离子型和阴离子型乳化剂,如聚氧乙烯脂肪酸酯、聚氧乙烯脂肪醇醚例如烷基芳基聚乙二醇醚、烷基磺酸酯、烷基硫酸酯、芳基磺酸酯和白蛋白水解产物,作为分散剂适用的有:例如木素-亚硫酸盐废液和甲基纤维素。
在粉剂、粒剂或胶乳形式的制剂中,可以应用的粘合剂有如羧甲基纤维素以及天然的和人工合成的聚合物,如阿拉伯树胶、聚乙烯醇和聚乙酸乙烯酯,以及天然的磷酯:如脑磷脂和卵磷酯,和合成的磷酯。其他的添加剂可以是矿物油和植物油。
可以应用着色剂如无机颜料,例如氧化铁、二氧化钛和普鲁士蓝;有机染料,例如茜素染料、偶氮染料和金属酞菁染料;还可以应用微量营养物例如铁盐、锰盐、硼盐、铜盐、钴盐、钼盐和锌盐。
所述制剂通常含有0.1~95%,优选0.5~90%(按重量计)的活性化合物。
本发明的活性化合物组合物可以与其它已知活性化合物,如杀真菌剂、杀虫剂、杀螨剂和除草剂一起以混合物的形式存在于上述制剂中,也可与肥料或植物生长调节剂一起以混合物的形式存在于上述制剂中。
可以应用活性化合物组合物本身,或者应用其制剂,或应用其备用形式,如现成的溶液剂、乳油、乳剂、悬浮剂、可湿性粉剂、可溶性粉剂和粒剂。
本发明活性化合物组合物可以按常规的方法施用,例如浇洒、喷雾、喷撒、散布、喷粉、涂刷、作为粉剂用于干燥的种子处理,作为溶液用于种子处理,作为水可溶的粉剂用于种子处理,作为水可分散的粉剂用于浆液处理或者拌种。
在处理植物各部分中,应用形式中活性化合物浓度可以在相当大的范围内变化。一般来讲,活性化合物的浓度可以为1~0.0001%,优选为0.5~0.001%(按重量计)。
在处理种子时,通常需要的活性化合物的用量为每公斤种子用0.001~50克,优选为0.01~10克。
对于土壤处理,在作用场所需要的活性化合物的浓度为0.00001~0.1%,优选为0.0001~0.02%(按重量计)。
本发明活性化合物组合物良好的杀真菌作用可以由下述实施例表明。虽然单个活性化合物的杀真菌作用是差的,但是其组合物显示出超过简单加合的作用。
如果活性化合物组合物的杀真菌作用大于单个施用的活性化合物作用的总和,那么该杀真菌剂组合物具有增效作用。
两个活性化合物组成的给定组合物的预期作用可以计算如下(参见Colby,S.R.,“Calculating Synergistic and AntagonisticResponses of Herbicide Combination”,Weeds 15,p20-22,1967);如果X表示与未处理的对照相比以浓度m(ppm)应用活性化合物A的效果水平(degree of efficacy)(以%表示),
Y表示与未处理的对照相比以浓度n(ppm)应用活性化合物B的效果水平(以%表示),
E表示与未处理的对照相比以浓度m和n(ppm)应用活性化合物A和B的预期效果水平(以%表示),那么 如果实际的杀真菌作用大于计算的结果,那么所述组合物的作用是超加合性的,即有增效作用。在该情况下,实际观察的效果水平必定大于从上式计算的效果水平的预期值(E)。
具体实施方式
实施例1
葡萄孢菌试验(大豆)/保护作用
为了得到活性化合物的合适制备物,将市购的活性化合物制剂(单一的活性化合物或活性化合物的组合物)用水稀释至各种情况下所需的浓度。
为了试验保护效果,幼苗用活性化合物的制备物喷洒直至湿透。喷洒后使表面处理层干燥,将覆盖有灰色葡萄孢菌的两小片琼脂置于各叶片上。将接种的植物置于20℃暗的湿润小室内。
接种3天后,评价叶片上侵染的斑点大小。
为了说明本试验中应用的活性化合物之间的增效作用,用Colby所述方法(见上面)评价结果。活性化合物、活性化合物浓度和试验结果见下表。
表1
葡萄孢菌试验(大豆)/保护作用活性化合物 活性化合物浓度 与未处理的对照相比
表1
葡萄孢菌试验(大豆)/保护作用活性化合物 活性化合物浓度 与未处理的对照相比
表1
葡萄孢菌试验(大豆)/保护作用活性化合物 活性化合物浓度 与未处理的对照相比
表1
葡萄孢菌试验(大豆)/保护作用活性化合物 活性化合物浓度 与未处理的对照相比
表1
葡萄孢菌试验(大豆)/保护作用活性化合物 活性化合物浓度 与未处理的对照相比
表1
葡萄孢菌试验(大豆)/保护作用活性化合物 活性化合物浓度 与未处理的对照相比
表1
葡萄孢菌试验(大豆)/保护作用活性化合物 活性化合物浓度 与未处理的对照相比
表1
葡萄孢菌试验(大豆)/保护作用活性化合物 活性化合物浓度 与未处理的对照相比
小球腔菌(Leptosphaeria nodorum)试验(小麦)/保护作用溶剂:100份(按重量计)二甲基甲酰胺乳化剂:0.25份(按重量计)烷基芳基聚乙二醇醚
为了得到活性化合物的合适制备物,将1份(按重量计)活性化合物与所述量的溶剂和乳化剂混合,并将液溶液用水稀释至所需的浓度。
为了试验保护效果,将幼苗用活性化合物的制备物喷洒直至湿润。喷洒后使表面处理层干燥,再用小球腔菌的孢子悬浮液喷洒幼苗。将幼苗置于20℃和100%相对大气湿度的保温小室内保持48小时。
将幼苗置于15℃的温度和约80%相对大气湿度的温室中。
接种10天后进行效果评价。
本试验表明,本发明下述化合物制备物实施例的效果明显优于先有技术。
表2
小球腔菌试验(小麦)/保护作用活性化合物 喷雾液中的活性化合物 与未处理的对照相
浓度(ppm) 比的效果(%)Febuconazole 25 75Tebuconazole+(I) 12,5 100(1∶1) + 12,5实施例3
白粉病菌试验(大麦)/保护作用溶剂:10份(按重量计)N-甲基吡咯烷酮乳化剂:0.6份(按重量计)烷基芳基聚乙二醇醚
为了得到活性化合物的合适制备物,将1份(按重量计)活性化合物与所述量的溶剂和乳化剂混合,将浓溶液用水稀释至所需的浓度。
为了试验保护效果,将幼苗用活性化合物的制备物喷洒直至湿润。喷洒后使表面处理层干燥,再用麦类白粉病菌f.SP.hordei孢子涂敷幼苗。
将幼苗置于约20℃的温度和约80%相对大气湿度的温室中,以便促进粉状霉菌色斑的发展。
接种7天后进行效果评价。
本试验表明,本发明下述化合物制备物实施例的效果明显优于先有技术。
表3:白粉病菌试验(大麦)/保护作用
本发明混合物:
25 100
(I)+(ηb) + 25
(1,0∶1)
(I)+(ηa) 25 58
(1,0∶1) + 25实施例4
白粉病菌试验(小麦)/保护作用溶剂:10份(按重量计)N-甲基吡咯烷酮乳化剂:0.6份(按重量计)烷基芳基聚乙二醇醚
为了得到活性化合物的合适制备物,将1份(按重量计)活性化合物与所述量的溶剂和乳化剂混合,将浓溶液用水稀释至所需的浓度。
为了试验保护效果,将幼苗用麦类白粉病菌f.sp.hordei孢子涂敷。接种后48小时,用活性化合物的制备物喷洒幼苗直至湿润。
将幼苗置于约20℃的温度和约80%相对大气湿度的温室中,以便促进粉状霉菌色斑的发展。
接种7天后进行效果评价。
本试验表明,本发明下述化合物制备物实施例的效果明显优于先有技术。
表4:白粉病菌试验(小麦)/保护作用
本发明混合物:
12,5 100
(I)+(ηb) + 12,5
(1,0∶1)
(I)+(ηa) 100 94
(1,0∶1) + 100实施例5
白粉病菌试验(小麦)/治疗作用溶剂:10份(按重量计)N-甲基吡咯烷酮乳化剂:0.6份(按重量计)烷基芳基聚乙二醇醚
为了得到活性化合物的合适制备物,将1份(按重量计)活性化合物与所述量的溶剂和乳化剂混合,将浓溶液用水稀释至所需的浓度。
为了试验治疗效果,将幼苗用麦类白粉病菌f.sp.hordei孢子涂敷。接种后48小时,用活性化合物的制备物喷洒幼苗直至湿润。
将幼苗置于约20℃的温度和约80%相对大气湿度的温室中,以便促进粉状霉菌色斑的发展。
接种7天后进行效果评价。
本试验表明,本发明下述化合物制备物实施例的效果明显优于先有技术。
表5
本发明混合物:
100 96
(I)+(ηa) + 100
(1,0∶1)
实施例6
小球腔菌试验(小麦)/治疗作用溶剂:10份(按重量计)二甲基甲酰胺乳化剂:0.6份(按重量计)烷基芳基聚乙二醇醚
为了得到活性化合物的合适制备物,将1份(按重量计)活性化合物与所述量的溶剂和乳化剂混合,将浓溶液用水稀释至所需的浓度。
为了试验治疗效果,将幼苗用活性化合物的制备物喷洒至湿润。喷洒后使表面处理层干燥,再用小球腔菌孢子悬浮液喷洒幼苗。将幼苗置于20℃和100%相对大气湿度的保温小室内保持48小时。
将幼苗置于15℃温度和约80%相对大气湿度的温室中。
接种10天后进行效果评价。
本试验表明,本发明下述化合物制备物实施例的效果明显优于先有技术。
表6
小球腔菌试验(小麦)/治疗作用
本发明混合物:
200 81
(I)+(ηb) + 200
(1,0∶1)
实施例7
条纹病试验(大麦)/保护作用溶剂:10份(按重量计)N-甲基吡咯烷酮乳化剂:0.6份(按重量计)烷基芳基聚乙二醇醚
为了得到活性化合物的合适制备物,将1份(按重量计)活性化合物与所述量的溶剂和乳化剂混合,将浓溶液用水稀释至所需的浓度。
为了试验保护效果,将幼苗用活性化合物的制备物喷洒直至湿润。喷洒后使表面处理层干燥,再用大麦条纹病的分生孢子悬浮液喷洒幼苗。然后将幼苗置于20℃和100%相对大气湿度的保温小室内保持48小时。
将幼苗置于约20℃的温度和约80%相对大气湿度的温室中。
接种7天后进行效果评价。
本试验表明,本发明下述化合物制备物实施例的效果明显优于先有技术。
表7
条纹病试验(大麦)/保护作用
本发明混合物:
12,5 75
(I)+(ηb) + 12,5
(1,0∶1)
Claims (5)
2.按照权利要求1所述的组合物,其特征在于:在活性化合物组合物中,式(I)活性化合物
-与活性化合物(δ)组的重量比为1∶0.5~1∶10,
-与活性化合物(β)组的重量比为1∶0.5~1∶10,
-与活性化合物(γ)组的重量比为1∶0.5~1∶10。
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EP2499911A1 (en) * | 2011-03-11 | 2012-09-19 | Bayer Cropscience AG | Active compound combinations comprising fenhexamid |
CN103300004B (zh) * | 2012-03-16 | 2016-02-17 | 陕西韦尔奇作物保护有限公司 | 一种含有环酰菌胺与甲氧基丙烯酸酯类的杀菌组合物 |
CN103300041B (zh) * | 2012-03-17 | 2016-04-06 | 陕西韦尔奇作物保护有限公司 | 一种含环酰菌胺的增效杀菌组合物 |
CN105685032A (zh) * | 2012-03-17 | 2016-06-22 | 陕西韦尔奇作物保护有限公司 | 一种含环酰菌胺的增效杀菌组合物 |
CN103300027A (zh) * | 2012-03-17 | 2013-09-18 | 陕西韦尔奇作物保护有限公司 | 一种含环酰菌胺的杀菌组合物 |
CN103314964A (zh) * | 2012-03-20 | 2013-09-25 | 陕西韦尔奇作物保护有限公司 | 一种含环酰菌胺与三唑类的农药组合物 |
CN103314982B (zh) * | 2012-03-20 | 2016-06-08 | 陕西韦尔奇作物保护有限公司 | 一种含环酰菌胺的农药组合物 |
CN103314967B (zh) * | 2012-03-21 | 2016-02-17 | 陕西韦尔奇作物保护有限公司 | 一种含有环酰菌胺的杀菌组合物 |
CN103314989B (zh) * | 2012-03-23 | 2016-08-03 | 陕西韦尔奇作物保护有限公司 | 一种含环酰菌胺与三唑类化合物的杀菌组合物 |
CN103355298B (zh) * | 2012-03-29 | 2016-04-06 | 陕西韦尔奇作物保护有限公司 | 一种含环酰菌胺与抗生素类的杀菌组合物 |
CN103828811A (zh) * | 2013-11-28 | 2014-06-04 | 广东中迅农科股份有限公司 | 一种含有环酰菌胺和氟啶胺的农药组合物 |
CN106561698A (zh) * | 2015-09-02 | 2017-04-19 | 陕西上格之路生物科学有限公司 | 一种含环酰菌胺的杀菌组合物 |
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KR102095352B1 (ko) * | 2018-09-05 | 2020-03-31 | 주식회사 드림테크 | 경추 교정장치 |
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EP0092158A3 (en) * | 1982-04-21 | 1985-11-27 | Mitsubishi Kasei Corporation | Thiazolidine compound and fungicidal composition containing it |
DE3431856A1 (de) * | 1984-08-30 | 1986-03-06 | Bayer Ag, 5090 Leverkusen | Fungizide mittel auf acylanilin-derivat-basis |
US4705800A (en) * | 1985-06-21 | 1987-11-10 | Ciba-Geigy Corporation | Difluorbenzodioxyl cyanopyrrole microbicidal compositions |
DE3814505A1 (de) * | 1988-04-29 | 1989-11-09 | Bayer Ag | Substituierte cycloalkyl- bzw. heterocyclyl-carbonsaeureanilide |
DE4012712A1 (de) * | 1989-09-02 | 1991-05-02 | Bayer Ag | Derivate carbocyclischer anilide |
EP0416315B1 (de) * | 1989-09-02 | 1994-11-30 | SABO-Maschinenfabrik GmbH | Häcksler zum Zerkleinern von Gartenabfällen mit einem Schneidwerk |
GB9320744D0 (en) * | 1992-11-04 | 1993-12-01 | Zeneca Ltd | Oxa and thiadiazole derivatives |
DE4313867A1 (de) * | 1993-04-28 | 1994-11-03 | Bayer Ag | Fungizide Wirkstoffkombinationen |
DE4437048A1 (de) * | 1994-10-17 | 1996-04-18 | Bayer Ag | Fungizide Wirkstoffkombinationen |
-
1993
- 1993-04-28 DE DE4313867A patent/DE4313867A1/de not_active Withdrawn
-
1994
- 1994-04-07 TR TR00334/94A patent/TR27417A/xx unknown
- 1994-04-12 TW TW083103201A patent/TW272111B/zh not_active IP Right Cessation
- 1994-04-15 ES ES94105879T patent/ES2099501T3/es not_active Expired - Lifetime
- 1994-04-15 EP EP94105879A patent/EP0626135B1/de not_active Expired - Lifetime
- 1994-04-15 DE DE59402194T patent/DE59402194D1/de not_active Expired - Lifetime
- 1994-04-22 JP JP10615694A patent/JP3491845B2/ja not_active Expired - Fee Related
- 1994-04-25 KR KR1019940008724A patent/KR100327775B1/ko not_active IP Right Cessation
- 1994-04-26 ZA ZA942887A patent/ZA942887B/xx unknown
- 1994-04-28 CN CN94104652A patent/CN1074902C/zh not_active Expired - Fee Related
- 1994-04-28 CN CNB001270753A patent/CN1157115C/zh not_active Expired - Fee Related
-
1995
- 1995-06-05 US US08/462,408 patent/US5532262A/en not_active Expired - Lifetime
-
1996
- 1996-04-08 US US08/629,245 patent/US5672619A/en not_active Expired - Lifetime
-
1997
- 1997-05-01 US US08/846,872 patent/US5922762A/en not_active Expired - Lifetime
-
1999
- 1999-02-12 US US09/249,690 patent/US6071940A/en not_active Expired - Fee Related
-
2000
- 2000-04-03 US US09/541,950 patent/US6235744B1/en not_active Expired - Fee Related
- 2000-09-14 CN CN00127076A patent/CN1131670C/zh not_active Expired - Fee Related
- 2000-12-14 US US09/736,917 patent/US6365195B2/en not_active Expired - Fee Related
-
2001
- 2001-08-03 HK HK01105410A patent/HK1034645A1/xx not_active IP Right Cessation
- 2001-08-03 HK HK01105416A patent/HK1034646A1/xx not_active IP Right Cessation
- 2001-12-13 US US10/022,136 patent/US6776994B2/en not_active Expired - Fee Related
-
2004
- 2004-06-03 US US10/860,868 patent/US7776906B2/en not_active Expired - Fee Related
-
2008
- 2008-05-09 US US12/118,212 patent/US20090074887A1/en not_active Abandoned
-
2010
- 2010-07-08 US US12/832,460 patent/US20110003011A1/en not_active Abandoned
Also Published As
Publication number | Publication date |
---|---|
DE59402194D1 (de) | 1997-04-30 |
HK1034646A1 (en) | 2001-11-02 |
CN1074902C (zh) | 2001-11-21 |
EP0626135B1 (de) | 1997-03-26 |
US6235744B1 (en) | 2001-05-22 |
EP0626135A2 (de) | 1994-11-30 |
US5672619A (en) | 1997-09-30 |
US20040220271A1 (en) | 2004-11-04 |
US20110003011A1 (en) | 2011-01-06 |
DE4313867A1 (de) | 1994-11-03 |
JP3491845B2 (ja) | 2004-01-26 |
US5532262A (en) | 1996-07-02 |
US6776994B2 (en) | 2004-08-17 |
ES2099501T3 (es) | 1997-05-16 |
US20010044443A1 (en) | 2001-11-22 |
EP0626135A3 (de) | 1995-02-01 |
CN1293896A (zh) | 2001-05-09 |
US6365195B2 (en) | 2002-04-02 |
CN1094221A (zh) | 1994-11-02 |
HK1034645A1 (en) | 2001-11-02 |
CN1293893A (zh) | 2001-05-09 |
JPH06329505A (ja) | 1994-11-29 |
KR100327775B1 (ko) | 2004-12-17 |
US5922762A (en) | 1999-07-13 |
ZA942887B (en) | 1995-01-04 |
US20020111385A1 (en) | 2002-08-15 |
TR27417A (tr) | 1995-04-14 |
KR940023360A (ko) | 1994-11-17 |
US6071940A (en) | 2000-06-06 |
TW272111B (zh) | 1996-03-11 |
US7776906B2 (en) | 2010-08-17 |
CN1157115C (zh) | 2004-07-14 |
US20090074887A1 (en) | 2009-03-19 |
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