WO2018040775A1 - Germicide composition - Google Patents

Germicide composition Download PDF

Info

Publication number
WO2018040775A1
WO2018040775A1 PCT/CN2017/093551 CN2017093551W WO2018040775A1 WO 2018040775 A1 WO2018040775 A1 WO 2018040775A1 CN 2017093551 W CN2017093551 W CN 2017093551W WO 2018040775 A1 WO2018040775 A1 WO 2018040775A1
Authority
WO
WIPO (PCT)
Prior art keywords
cyproconazole
composition according
bactericidal composition
composition
adjuvant
Prior art date
Application number
PCT/CN2017/093551
Other languages
French (fr)
Chinese (zh)
Inventor
仲汉根
季自华
季红进
花伟
Original Assignee
江苏辉丰农化股份有限公司
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by 江苏辉丰农化股份有限公司 filed Critical 江苏辉丰农化股份有限公司
Publication of WO2018040775A1 publication Critical patent/WO2018040775A1/en

Links

Classifications

    • 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
    • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/64—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with three nitrogen atoms as the only ring hetero atoms
    • A01N43/647—Triazoles; Hydrogenated triazoles
    • A01N43/653—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
    • 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
    • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
    • A01N43/80—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms five-membered rings with one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,2

Definitions

  • the invention belongs to the field of agricultural plant protection, in particular to a germicidal composition with improved properties, in particular to a germicidal composition comprising benzisothiazolinones and cyproconazole.
  • Benzoisothiazolinones are a new type of broad-spectrum fungicide mainly used for the prevention and treatment of various bacterial and fungal diseases such as cereal crops, vegetables and fruits.
  • the mechanism of bactericidal action mainly includes destroying the nuclear structure of the pathogen, causing it to lose the heart part and failing to death and interfering with the metabolism of the pathogenic cells, causing its physiological disorder and ultimately leading to death. It can effectively protect plants from pathogens in the early stage of disease occurrence. Increasing the dosage after disease occurrence can obviously control the spread of pathogens, thus achieving the dual functions of protection and eradication.
  • Cyproconazole is a triazole fungicide with preventive, therapeutic and systemic effects. Applicable to wheat, barley, oats, corn, sorghum, beets, apples, pears and other plants, can effectively prevent diseases caused by powdery mildew, rust fungus, Fusarium, nucleocapsid, and genus . Its bactericidal action is characterized by steroid demethylation (ergosterol biosynthesis) inhibitors, which are rapidly absorbed by the plant's viable part and transferred mainly to the top.
  • steroid demethylation ergosterol biosynthesis
  • the object of the present invention is to solve the resistance of the bactericide in practical application and the problem of soil residue, and to screen out the fungicides with different sterilization principles to obtain a new fungicide composition, so as to improve the control effect of the bactericide and delay the resistance.
  • Sexual production reducing the amount of application, reducing the cost of prevention.
  • Another object of the present invention is to provide a process for the preparation of a bactericidal composition comprising two active ingredients A and B and for the control of crop diseases in the agricultural sector.
  • the object of the invention can be achieved by the following measures:
  • a synergistic biocide composition comprising two active components A and B, wherein active component A is a structural compound having formula (I) and active component B is cyproconazole.
  • R is selected from H or a C 1 - C 8 alkyl group.
  • the C 1 -C 8 alkyl group in the present invention means a linear or branched alkyl group having 1 to 8 carbon atoms, and includes a C 1 alkyl group (e.g., methyl group) and a C 2 alkyl group (e.g., ethyl group). , C 3 alkyl (such as n-propyl, isopropyl), C 4 alkyl (such as n-butyl, isobutyl, tert-butyl, sec-butyl), C 5 alkyl (such as n-pentyl, etc.) , C 6 alkyl, C 7 alkyl, C 8 alkyl. It includes, but is not limited to, C 1 -C 6 alkyl, C 1 -C 5 alkyl, C 1 -C 4 alkyl, and the like.
  • R is selected from H or a C 1 -C 4 alkyl group.
  • R is selected from the group consisting of H, -CH 3 or -C 4 H 9 .
  • A is 1,2-benzisothiazolin-3-one (abbreviated as BIT in the specification).
  • R is CH 3
  • A is 2-methyl-1,2-benzisothiazolin-3-one (abbreviated as MBIT in the specification).
  • R is C 4 H 9
  • A is 2-butyl-1,2-benzisothiazolin-3-one
  • the "butyl group” in the formula is preferably n-butyl (instruction Referred to as BBIT).
  • the inventors have found through experiments that the composition of the present invention is effective for controlling bacterial or fungal diseases of crops, and more importantly, the application amount is reduced and the use cost is lowered.
  • the compounds containing component A and component B have different structural types and different mechanisms of action. The combination of the two can expand the bactericidal spectrum, and can delay the generation and development of pathogen resistance to a certain extent, and component A and group There is no cross-resistance between points B.
  • the weight ratio between the two components in the bactericide composition of the present invention is from 10 to 1:1 to 30.
  • the weight ratio between the components of component A and component B can be further optimized to 1:1-20.
  • the weight ratio between the two components of A and B can be arbitrarily adjusted within the range of the following ratios: 10:1, 9:1, 8:1, 7:1, 6:1 5:1, 4:1, 3:1, 2:1, 1:1, 1:2, 1:3, 1:4, 1:5, 1:6, 1:7, 1:8, 1: 9, 1:10, 1:11, 1:12, 1:13, 1:14, 1:15, 1:16, 1:17, 1:18, 1:19, 1:20, 1:21, 1:22, 1:23, 1:24, 1:25, 1:26, 1:27, 1:28, 1:29, 1:30, or within the range of any two of the above ratios Selection is made, and these ratios can be understood as weight ratios, and may also include molar ratios.
  • composition of the present invention can be made into a pesticide-acceptable dosage form from the active ingredient and agrochemical adjuvant or adjuvant. Further, the composition comprises from 2 to 80% by weight of the active component and 98 to 20% by weight of the pesticide adjuvant or auxiliary compound. The approved dosage form.
  • the present invention provides the use of a bactericidal composition comprising component A and component B for controlling crop diseases in the agricultural sector, in particular for controlling fungi or bacteria of certain crops.
  • composition may specifically comprise an agrochemical adjuvant or an auxiliary such as one or more of a carrier, a solvent, a dispersing agent, a wetting agent, an adhesive, a thickener, a binder, a surfactant or a fertilizer.
  • auxiliary such as one or more of a carrier, a solvent, a dispersing agent, a wetting agent, an adhesive, a thickener, a binder, a surfactant or a fertilizer.
  • auxiliary such as one or more of a carrier, a solvent, a dispersing agent, a wetting agent, an adhesive, a thickener, a binder, a surfactant or a fertilizer.
  • auxiliary such as one or more of a carrier, a solvent, a dispersing agent, a wetting agent, an adhesive, a thickener, a binder, a surfactant or a fertilizer.
  • Common auxiliaries can be mixed during the application.
  • auxiliaries or auxiliaries may be solid or liquid, they are usually materials commonly used in the processing of dosage forms, such as natural or regenerated minerals, solvents, dispersants, wetting agents, adhesives, thickeners, binders. .
  • the method of application of the compositions of the invention comprises the use of the compositions of the invention for aerial parts of plants, in particular leaves or foliage. You can choose to soak or apply to the surface of the control object.
  • the frequency of administration and the amount administered will depend on the biological and climatic conditions of the pathogen.
  • the plant growth site such as rice fields, may be wetted with a liquid formulation of the composition, or the composition may be applied to the soil in solid form, such as in the form of granules (soil application), the composition may be passed from the soil to the plant through the roots of the plant. In vivo (systemic action).
  • composition of the present invention can be prepared into various pesticide-acceptable dosage forms including, but not limited to, emulsifiable concentrates, suspending agents, wettable powders, water-dispersible granules, powders, granules, aqueous preparations, aqueous emulsions, microemulsions, poison baits.
  • the dosage form of the invention employs a wettable powder, a suspending agent, a water-dispersible granule, an aqueous emulsion or a microemulsion.
  • the compositions may be applied by spraying, misting, dusting, spreading or pouring, and the like.
  • composition of the present invention can be prepared into various dosage forms by a known method, and the active ingredient and the auxiliary agent, such as a solvent, a solid carrier, and, if necessary, can be uniformly mixed and ground together with the surfactant to prepare a desired preparation. Dosage form.
  • the above solvent may be selected from aromatic hydrocarbons, preferably containing from 8 to 12 carbon atoms, such as a mixture of xylenes or substituted benzenes, phthalates such as dibutyl phthalate or dicaprylic acid, aliphatic hydrocarbons such as rings.
  • aromatic hydrocarbons preferably containing from 8 to 12 carbon atoms, such as a mixture of xylenes or substituted benzenes, phthalates such as dibutyl phthalate or dicaprylic acid, aliphatic hydrocarbons such as rings.
  • Alkenes or paraffins, alcohols and glycols and their ethers and esters such as ethanol, ethylene glycol, ethylene glycol monomethyl
  • ketones such as cyclohexanone
  • highly polar solvents such as N-methyl-2 Pyrrolidone, dimethyl sulfoxide or dimethylformamide
  • vegetable or vegetable oils such as soybean oil.
  • the above solid carriers are typically natural mineral fillers such as talc, kaolin, montmorillonite or activated clay.
  • a highly dispersible silicic acid or a highly dispersible adsorbent polymer carrier such as a particulate adsorbent carrier or a non-adsorbing carrier, and a suitable particulate adsorbent carrier is porous, such as pumice, bentonite or Bentonite; a suitable non-adsorbing carrier such as calcite or sand.
  • a large amount of pre-granulated materials of inorganic or organic nature can be used as a carrier, in particular dolomite.
  • Suitable surfactants are lignosulfonic acid, naphthalenesulfonic acid, phenolsulfonic acid, alkaline earth metal or amine salts, alkylarylsulfonates, alkyl groups Sulfates, alkyl sulfonates, fatty alcohol sulphates, fatty acids and sulfated fatty alcohol glycol ethers, as well as condensates of sulfonated naphthalene and naphthalene derivatives with formaldehyde, naphthalene or naphthalene sulfonic acid with phenol and formaldehyde Condensate, polyoxyethylene octyl phenyl ether, ethoxylated isooctyl phenol, octyl phenol, nonyl phenol, alkyl aryl polyglycol ether, tributyl benzene poly
  • the active ingredient A can be first dissolved in certain specific basic substances to form a benzisothiazolin metal salt.
  • suitable basic substances include: alkali metal carbonates, alkali metal hydrogens Oxide (such as sodium hydroxide, potassium hydroxide), alkali metal alkoxy carbonate, alkali metal alkoxide or magnesium methoxide.
  • the two active ingredients in the compositions of the present invention exhibit synergistic effects, the activity of which is more pronounced than the expected sum of activity using a single compound, and the individual activity of a single compound.
  • the synergistic effect is manifested by allowing for a reduced application rate, a broader fungicidal control profile, quicker effect, longer lasting control effect, better control of plant harmful fungi by only one or a few applications, and broadening of possible application. Intervals. These properties are particularly desirable in the practice of plant fungi control.
  • the fungicide composition of the invention can be applied to the agricultural field for controlling crop diseases, such as tomato early blight, sweet pepper white star disease, pumpkin mosaic virus disease, grape downy mildew, wheat sheath blight, citrus anthracnose, etc.
  • the invention can also control other diseases of crops, including but not limited to wheat diseases (such as wheat scab, wheat powdery mildew, wheat rust, etc.), rice diseases (such as rice sheath blight, rice smut, rice blast, Rice bacterial streaks, etc., corn diseases (such as: corn smut, corn big spot disease, corn small spot disease), cucumber diseases (such as: cucumber downy mildew, cucumber powdery mildew, cucumber anthracnose, cucumber bacterial Angle spot disease, etc., tomato diseases (such as: tomato anthracnose, tomato gray mold, tomato bacterial angular spot disease, etc.), grape diseases (such as: grape gray mold, grape powdery mildew), apple disease (such as apple wheel) Phytophthora, apple anthrac
  • the other characteristics exhibited by the bactericidal composition of the present invention are mainly as follows: 1.
  • the compounding of the composition of the present invention has obvious synergistic effect; 2. Since the chemical composition of the two single agents of the present composition is greatly different, the effect The mechanism is completely different, there is no cross-resistance, and the problem of resistance caused by the separate use of the two single agents can be delayed; 3.
  • the composition of the present invention is safe and safe for crops. It has been proved by experiments that the bactericidal composition of the invention has stable chemical properties, remarkable synergistic effect, and exhibits obvious synergistic effect and complementary effect on the control object.
  • the active ingredient active group A and the active component B, and the auxiliary agent and the filler are uniformly mixed according to the formula, and are pulverized into a wettable powder by a jet stream, and then added with a certain amount of water to be mixed and extruded, granulated, and dried and sieved.
  • a water dispersible granule product A water dispersible granule product.
  • Example 2 52% BIT ⁇ cyproconazole water dispersible granules
  • Example 3 12% MBIT ⁇ cyproconazole water dispersible granules
  • Example 4 52% MBIT ⁇ cyproconazole water-dispersible granules
  • Example 5 12% BBIT ⁇ cyproconazole water dispersible granules
  • Example 6 52% BBIT ⁇ cyproconazole water dispersible granules
  • the active ingredient active group A and the active component B, and the components such as a dispersing agent, a wetting agent, a thickener and water are uniformly mixed according to the formula, and after being sanded and/or sheared at a high speed, a semi-finished product is obtained. After the analysis, the water is mixed and evenly filtered to obtain the finished product.
  • Example 7 11% BIT ⁇ cyproconazole suspending agent
  • Example 8 50% BIT ⁇ cyproconazole suspension
  • Example 9 31.5% BIT ⁇ cyproconazole suspension
  • Example 10 11% MBIT ⁇ cyproconazole suspension
  • Example 11 50% MBIT ⁇ cyproconazole suspension
  • Example 12 31.5% MBIT ⁇ cyproconazole suspension
  • Example 13 11% BBIT ⁇ cyproconazole suspending agent
  • Example 14 50% BBIT ⁇ cyproconazole suspension
  • Example 15 31.5% BBIT ⁇ cyproconazole suspension
  • the active ingredients A and B active ingredients are mixed with various auxiliaries and fillers in proportion, and the ultrafine pulverizer powder is mixed. After being crushed, a wettable powder is obtained.
  • Example 16 55% BIT ⁇ cyproconazole wettable powder (1:10)
  • Example 17 31% BIT ⁇ cyproconazole wettable powder (1:30)
  • Example 18 55% MBIT ⁇ cyproconazole wettable powder
  • MBIT was 5%
  • cyproconazole 50%
  • the remaining components were prepared in the same manner as in Example 16.
  • Example 19 31% MBIT ⁇ cyproconazole wettable powder
  • Example 20 55% BBIT ⁇ cyproconazole wettable powder
  • Example 21 31% BBIT ⁇ cyproconazole wettable powder
  • the control effect is converted into the probability value (y), the liquid height ( ⁇ g/ml) is converted into a logarithmic value (x), the virulence equation is calculated by the least squares method, and the neutral concentration EC50 is suppressed, and the virulence of the drug is calculated according to the method of Sun Yunpei. Exponential Co-toxicity Factor (CTC).
  • CTC Exponential Co-toxicity Factor
  • Measured virulence index (ATI) (standard drug EC50 / test drug EC50) * 100
  • Theoretical virulence index (TTI) A virulence index * Percentage of A in the mixture + B virulence index * Percentage of B in the mixture
  • CTC Co-toxicity coefficient [mixture measured virulence index (ATI) / mixed theory virulence index (TTI)] * 100
  • CTC ⁇ 80 the composition showed antagonism, 80 ⁇ CTC ⁇ 120, the composition showed an additive effect, CTC ⁇ 120, and the composition showed synergistic effect.
  • Test method In the early stage of the disease, the first spray was immediately performed, and after 7 days, the second application was carried out, each treatment of 4 cells, 20 square meters per cell. The incidence of the disease was investigated before the drug and 11 days after the second drug. Each plot was randomly sampled at 5 points, and 5 crops were investigated at each point. The percentage of the lesion area per leaf on the whole plant was counted and graded. Disease index and control effect.
  • Grade 1 less than 5 leaf lesions, less than 1 cm in length;
  • Grade 3 6-10 leaf lesions, some lesions are longer than 1 cm;
  • Grade 5 11-25 leaf lesions, some lesions are connected into pieces, and the lesion area accounts for 10-25% of the leaf area;
  • Grade 7 more than 26 leaf lesions, the lesions are connected into pieces, and the lesion area accounts for 26-50% of the leaf area;
  • Grade 9 The lesions are connected into pieces, and the area of the lesions accounts for more than 50% of the leaf area or the whole leaves are dead.

Landscapes

  • 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

Provided is a germicide composition. The composition contains two active ingredients A and B, the active ingredient A being a compound having a structure of formula (I), the active ingredient B being cyproconazole, and the weight ratio between the two ingredients being 10-1:1-30. Further provided are a preparation method and use of the composition. Experimental results show that the above germicide composition has clear synergistic effects, and more importantly, a reduced application quantity and reduced usage costs. The germicide composition is effective in controlling certain bacterial or fungal diseases of crops. The compounding of germicides with different mechanisms and modes of action achieves favorable effects including expanding bactericidal spectrum, delaying fungal and bacterial resistance, and improving disease control effects.

Description

一种杀菌剂组合物Fungicide composition 技术领域Technical field
本发明属于农业植物保护领域，特别是涉及一种具有改进性能的杀菌组合物，具体地说是涉及一种包含苯并异噻唑啉酮类和环丙唑醇的杀菌组合物。The invention belongs to the field of agricultural plant protection, in particular to a germicidal composition with improved properties, in particular to a germicidal composition comprising benzisothiazolinones and cyproconazole.
背景技术Background technique
苯并异噻唑啉酮类化合物是一种新型、广谱杀菌剂，主要用于防治和治疗禾谷类作物、蔬菜、水果等多种细菌、真菌性病害。其杀菌作用机理，主要包括破坏病菌细胞核结构，使其失去心脏部位而衰竭死亡和干扰病菌细胞的新陈代谢，使其生理紊乱，最终导致死亡两个方面。在病害发生初期使用可有效保护植株不受病原物侵染，病害发生后酌情增加用药量可明显控制病菌的蔓延，从而达到保护和铲除的双重作用。Benzoisothiazolinones are a new type of broad-spectrum fungicide mainly used for the prevention and treatment of various bacterial and fungal diseases such as cereal crops, vegetables and fruits. The mechanism of bactericidal action mainly includes destroying the nuclear structure of the pathogen, causing it to lose the heart part and failing to death and interfering with the metabolism of the pathogenic cells, causing its physiological disorder and ultimately leading to death. It can effectively protect plants from pathogens in the early stage of disease occurrence. Increasing the dosage after disease occurrence can obviously control the spread of pathogens, thus achieving the dual functions of protection and eradication.
环丙唑醇(cyproconazole)属***类杀菌剂，具有预防、治疗、内吸作用。适用于小麦、大麦、燕麦、玉米、高粱、甜菜、苹果、梨等植物，可有效防治白粉菌属、柄锈菌属、喙孢属、核腔菌属和壳针孢属菌等引起的病害。其杀菌作用特点类固醇脱甲基化(麦角甾醇生物合成)抑制剂，能迅速被植物有生长力的部分吸收并主要向顶部转移。Cyproconazole is a triazole fungicide with preventive, therapeutic and systemic effects. Applicable to wheat, barley, oats, corn, sorghum, beets, apples, pears and other plants, can effectively prevent diseases caused by powdery mildew, rust fungus, Fusarium, nucleocapsid, and genus . Its bactericidal action is characterized by steroid demethylation (ergosterol biosynthesis) inhibitors, which are rapidly absorbed by the plant's viable part and transferred mainly to the top.
实际的农药经验已经表明，重复且专一施用一种活性化合物来防治有害真菌在很多情况下将导致真菌菌株的快速选择性，为降低抗性真菌菌株选择性的危险性，目前通常使用不同活性化合物的混合物来防治有害真菌。通过将具有不同作用机理的活性化合物进行组合，可延缓抗性产生，降低施用量，减少防治成本。Practical pesticide experience has shown that repeated and specific application of an active compound to control harmful fungi will in many cases lead to rapid selectivity of fungal strains, and in order to reduce the risk of selectivity of resistant fungal strains, different activities are currently used. A mixture of compounds to control harmful fungi. By combining active compounds having different mechanisms of action, resistance can be delayed, application rates can be reduced, and cost of control can be reduced.
发明内容Summary of the invention
本发明的目的是针对杀菌剂在实际应用中抗性以及土壤残留问题，筛选出不同杀菌原理的杀菌剂进行复配，得到新的一种杀菌剂组合物，以提高杀菌剂防治效果，延缓抗性产生，降低施用量，减少防治成本。The object of the present invention is to solve the resistance of the bactericide in practical application and the problem of soil residue, and to screen out the fungicides with different sterilization principles to obtain a new fungicide composition, so as to improve the control effect of the bactericide and delay the resistance. Sexual production, reducing the amount of application, reducing the cost of prevention.
本发明的另一个目的是提供包含两种有效成分A和B杀菌组合物的制备方法及在农业领域防治农作物病害的应用。Another object of the present invention is to provide a process for the preparation of a bactericidal composition comprising two active ingredients A and B and for the control of crop diseases in the agricultural sector.
本发明的目的可以通过以下措施达到：The object of the invention can be achieved by the following measures:
一种具有增效作用的杀菌剂组合物，该组合物包含A和B两种活性组分，其中活性组分A为具有式(Ⅰ)的结构化合物，活性组分B为环丙唑醇。 A synergistic biocide composition comprising two active components A and B, wherein active component A is a structural compound having formula (I) and active component B is cyproconazole.
Figure PCTCN2017093551-appb-000001
Figure PCTCN2017093551-appb-000001
式(Ⅰ)中，R选自H或C1～C8烷基。In the formula (I), R is selected from H or a C 1 - C 8 alkyl group.
本发明中的C1～C8烷基是指含有1至8个碳原子的直链或支链烷基，它包括C1烷基(如甲基)、C2烷基(如乙基)、C3烷基(如正丙基、异丙基)、C4烷基(如正丁基、异丁基、叔丁基、仲丁基)、C5烷基(如正戊基等)、C6烷基、C7烷基、C8烷基。它包括但不限于C1～C6烷基、C1～C5烷基、C1～C4烷基等。The C 1 -C 8 alkyl group in the present invention means a linear or branched alkyl group having 1 to 8 carbon atoms, and includes a C 1 alkyl group (e.g., methyl group) and a C 2 alkyl group (e.g., ethyl group). , C 3 alkyl (such as n-propyl, isopropyl), C 4 alkyl (such as n-butyl, isobutyl, tert-butyl, sec-butyl), C 5 alkyl (such as n-pentyl, etc.) , C 6 alkyl, C 7 alkyl, C 8 alkyl. It includes, but is not limited to, C 1 -C 6 alkyl, C 1 -C 5 alkyl, C 1 -C 4 alkyl, and the like.
在一种优选方案中，R选自H或C1～C4烷基。In a preferred embodiment, R is selected from H or a C 1 -C 4 alkyl group.
在一种更优选的方案中，R选自H、-CH3或-C4H9。In a more preferred embodiment, R is selected from the group consisting of H, -CH 3 or -C 4 H 9 .
式(Ⅰ)中，当R为H时，A为1,2-苯并异噻唑啉-3-酮(说明书中简称BIT)。In the formula (I), when R is H, A is 1,2-benzisothiazolin-3-one (abbreviated as BIT in the specification).
式(Ⅰ)中，当R为CH3时，A为2-甲基-1,2-苯并异噻唑啉-3-酮(说明书中简称MBIT)。In the formula (I), when R is CH 3 , A is 2-methyl-1,2-benzisothiazolin-3-one (abbreviated as MBIT in the specification).
式(Ⅰ)中，当R为C4H9时，A为2-丁基-1,2-苯并异噻唑啉-3-酮，该式中的“丁基”优选正丁基(说明书中简称BBIT)。In the formula (I), when R is C 4 H 9 , A is 2-butyl-1,2-benzisothiazolin-3-one, and the "butyl group" in the formula is preferably n-butyl (instruction Referred to as BBIT).
发明人通过试验发现，本发明的组合物是用于防治农作物细菌或真菌性病害防治增效明显，更重要的是施用量减少，降低使用成本。含有组分A与组分B的化合物结构类型不同，作用机制各异，两者复配能够扩大杀菌谱，并且可以在一定程度上延缓病原菌抗性的产生和发展速度，且组分A与组分B之间无交互抗性。The inventors have found through experiments that the composition of the present invention is effective for controlling bacterial or fungal diseases of crops, and more importantly, the application amount is reduced and the use cost is lowered. The compounds containing component A and component B have different structural types and different mechanisms of action. The combination of the two can expand the bactericidal spectrum, and can delay the generation and development of pathogen resistance to a certain extent, and component A and group There is no cross-resistance between points B.
本发明杀菌剂组合物中的两组分之间的重量比为10～1:1～30。为使两组分间的药效增效作用更为显著，组分A和组分B的重量两组分之间的重量比可以进一步优化至1：1～20。The weight ratio between the two components in the bactericide composition of the present invention is from 10 to 1:1 to 30. In order to make the synergistic effect between the two components more significant, the weight ratio between the components of component A and component B can be further optimized to 1:1-20.
一种优选的方案中，A和B两组分之间的重量比可以任意地在下述配比的范围内进行调整10:1、9:1、8:1、7:1、6:1、5:1、4:1、3:1、2:1、1:1、1:2、1:3、1:4、1:5、1:6、1:7、1:8、1:9、1:10、1:11、1:12、1:13、1:14、1:15、1:16、1:17、1:18、1:19、1:20、1:21、1:22、1:23、1:24、1:25、1:26、1:27、1:28、1:29、1:30,也可以在以上任意两个配比所组成的范围内进行选择，这些比例可以理解为重量比，也可以包括摩尔比。In a preferred embodiment, the weight ratio between the two components of A and B can be arbitrarily adjusted within the range of the following ratios: 10:1, 9:1, 8:1, 7:1, 6:1 5:1, 4:1, 3:1, 2:1, 1:1, 1:2, 1:3, 1:4, 1:5, 1:6, 1:7, 1:8, 1: 9, 1:10, 1:11, 1:12, 1:13, 1:14, 1:15, 1:16, 1:17, 1:18, 1:19, 1:20, 1:21, 1:22, 1:23, 1:24, 1:25, 1:26, 1:27, 1:28, 1:29, 1:30, or within the range of any two of the above ratios Selection is made, and these ratios can be understood as weight ratios, and may also include molar ratios.
本发明的组合物可以由活性成分和农药助剂或辅料制成农药上允许的剂型。进一步的，该组合物由2～80％重量份的活性组分与98～20％重量份的农药助剂或辅料组成农药 上允许的剂型。The composition of the present invention can be made into a pesticide-acceptable dosage form from the active ingredient and agrochemical adjuvant or adjuvant. Further, the composition comprises from 2 to 80% by weight of the active component and 98 to 20% by weight of the pesticide adjuvant or auxiliary compound. The approved dosage form.
本发明提供了包含组分A和组分B的杀菌组合物在农业领域防治农作物病害方面的用途，特别是在防治某些作物的真菌或细菌方面的用途。The present invention provides the use of a bactericidal composition comprising component A and component B for controlling crop diseases in the agricultural sector, in particular for controlling fungi or bacteria of certain crops.
上述组合物具体可包含农药助剂或辅料，例如载体、溶剂、分散剂、润湿剂、胶粘剂、增稠剂、粘合剂、表面活性剂或肥料等中的一种或几种。在施用的过程中可以混合常用的助剂。The above composition may specifically comprise an agrochemical adjuvant or an auxiliary such as one or more of a carrier, a solvent, a dispersing agent, a wetting agent, an adhesive, a thickener, a binder, a surfactant or a fertilizer. Common auxiliaries can be mixed during the application.
合适的助剂或辅料可以是固体或液体，它们通常是剂型加工过程中常用的物质，例如天然的或再生的矿物质，溶剂、分散剂、润湿剂、胶粘剂、增稠剂、粘合剂。Suitable auxiliaries or auxiliaries may be solid or liquid, they are usually materials commonly used in the processing of dosage forms, such as natural or regenerated minerals, solvents, dispersants, wetting agents, adhesives, thickeners, binders. .
本发明组合物的施用方法包括将本发明的组合物用于植物生长的地上部分，特别是叶部或叶面。可以选择浸种或涂抹于防治对象表面。施用的频率和施用量取决于病原体的生物学和气候生存条件。可以将植物的生长场所，如稻田，用组合物的液体制剂浸湿，或者将组合物以固体形式施用于土壤中，如以颗粒形式(土壤施用)，组合物可以由土壤经植物根部进入植物体内(内吸作用)。The method of application of the compositions of the invention comprises the use of the compositions of the invention for aerial parts of plants, in particular leaves or foliage. You can choose to soak or apply to the surface of the control object. The frequency of administration and the amount administered will depend on the biological and climatic conditions of the pathogen. The plant growth site, such as rice fields, may be wetted with a liquid formulation of the composition, or the composition may be applied to the soil in solid form, such as in the form of granules (soil application), the composition may be passed from the soil to the plant through the roots of the plant. In vivo (systemic action).
本发明的组合物可以制备成农药上可接受的各种剂型，包括但不限于乳油、悬浮剂、可湿性粉剂、水分散粒剂、粉剂、粒剂、水剂、水乳剂、微乳剂、毒饵、母液、母粉等，在一种优选方案中，本发明的剂型采用可湿性粉剂、悬浮剂、水分散粒剂、水乳剂或微乳剂。根据这些组合物的性质以及施用组合物所要达到的目的和环境情况，可以选择将组合物以喷雾、弥雾、喷粉、撒播或泼浇等之类的方法施用。The composition of the present invention can be prepared into various pesticide-acceptable dosage forms including, but not limited to, emulsifiable concentrates, suspending agents, wettable powders, water-dispersible granules, powders, granules, aqueous preparations, aqueous emulsions, microemulsions, poison baits. A mother liquor, a mother powder or the like. In a preferred embodiment, the dosage form of the invention employs a wettable powder, a suspending agent, a water-dispersible granule, an aqueous emulsion or a microemulsion. Depending on the nature of the compositions and the intended purpose and environmental conditions to which the compositions are to be applied, the compositions may be applied by spraying, misting, dusting, spreading or pouring, and the like.
可用已知的方法可以将本发明的组合物制备成各种剂型，可以将有效成分与助剂，如溶剂、固体载体，需要时可以与表面活性剂一起均匀混合、研磨，制备成所需要的剂型。The composition of the present invention can be prepared into various dosage forms by a known method, and the active ingredient and the auxiliary agent, such as a solvent, a solid carrier, and, if necessary, can be uniformly mixed and ground together with the surfactant to prepare a desired preparation. Dosage form.
上述的溶剂可选自芳香烃，优选含8-12个碳原子，如二甲苯混合物或取代的苯，酞酸酯类，如酞酸二丁酯或酞酸二辛酸，脂肪烃类，如环已烷或石蜡，醇和乙二醇和它们的醚和酯，如乙醇，乙二醇，乙二醇单甲基；酮类，如环已酮，强极性的溶剂，如N-甲基-2-吡咯烷酮，二甲基亚砜或二甲基甲酰胺，和植物油或植物油，如大豆油。The above solvent may be selected from aromatic hydrocarbons, preferably containing from 8 to 12 carbon atoms, such as a mixture of xylenes or substituted benzenes, phthalates such as dibutyl phthalate or dicaprylic acid, aliphatic hydrocarbons such as rings. Alkenes or paraffins, alcohols and glycols and their ethers and esters, such as ethanol, ethylene glycol, ethylene glycol monomethyl; ketones, such as cyclohexanone, highly polar solvents such as N-methyl-2 Pyrrolidone, dimethyl sulfoxide or dimethylformamide, and vegetable or vegetable oils such as soybean oil.
上述的固体载体，如用于粉剂和可分散剂的通常是天然矿物填料，例如滑石、高岭土，蒙脱石或活性白土。为了管理组合物的物理性能，也可以加入高分散性硅酸或高分散性吸附聚合物载体，例如粒状吸附载体或非吸附载体，合适的粒状吸附载体是多孔型的，如浮石、皂土或膨润土；合适的非吸附载体如方解石或砂。另外，可以使用大量的无机性质或有机性质的预制成粒状的材料作为载体，特别是白云石。 The above solid carriers, such as those used in powders and dispersibles, are typically natural mineral fillers such as talc, kaolin, montmorillonite or activated clay. In order to manage the physical properties of the composition, it is also possible to add a highly dispersible silicic acid or a highly dispersible adsorbent polymer carrier, such as a particulate adsorbent carrier or a non-adsorbing carrier, and a suitable particulate adsorbent carrier is porous, such as pumice, bentonite or Bentonite; a suitable non-adsorbing carrier such as calcite or sand. In addition, a large amount of pre-granulated materials of inorganic or organic nature can be used as a carrier, in particular dolomite.
根据本发明的组合物中的有效成分的化学性质，合适的表面活性剂为木质素磺酸、萘磺酸、苯酚磺酸、碱土金属盐或胺盐，烷基芳基磺酸盐，烷基硫酸盐，烷基磺酸盐，脂肪醇硫酸盐，脂肪酸和硫酸化脂肪醇乙二醇醚，还有磺化萘和萘衍生物与甲醛的缩合物，萘或萘磺酸与苯酚和甲醛的缩合物，聚氧乙烯辛基苯基醚，乙氧基化异辛基酚，辛基酚，壬基酚，烷基芳基聚乙二醇醚，三丁基苯聚乙二醇醚，三硬脂基苯基聚乙二醇醚，烷基芳基聚醚醇，乙氧基化蓖麻油，聚氧乙烯烷基醚，氧化乙烯缩合物、乙氧基化聚氧丙烯，月桂酸聚乙二醇醚缩醛，山梨醇酯，木质素亚硫酸盐废液和甲基纤维素。Suitable surfactants according to the chemical nature of the active ingredient in the composition of the present invention are lignosulfonic acid, naphthalenesulfonic acid, phenolsulfonic acid, alkaline earth metal or amine salts, alkylarylsulfonates, alkyl groups Sulfates, alkyl sulfonates, fatty alcohol sulphates, fatty acids and sulfated fatty alcohol glycol ethers, as well as condensates of sulfonated naphthalene and naphthalene derivatives with formaldehyde, naphthalene or naphthalene sulfonic acid with phenol and formaldehyde Condensate, polyoxyethylene octyl phenyl ether, ethoxylated isooctyl phenol, octyl phenol, nonyl phenol, alkyl aryl polyglycol ether, tributyl benzene polyglycol ether, three Stearyl phenyl polyglycol ether, alkyl aryl polyether alcohol, ethoxylated castor oil, polyoxyethylene alkyl ether, ethylene oxide condensate, ethoxylated polyoxypropylene, lauric acid poly Glycol ether acetal, sorbitol ester, lignin sulfite waste liquor and methyl cellulose.
在制备液体或固体剂型时，可以先将活性组分A溶于某些特定的碱性物质，形成苯并异噻唑啉金属盐，合适的碱性物质包括：碱金属碳酸盐、碱金属氢氧化物(如氢氧化钠、氢氧化钾)、碱金属烷氧基碳酸盐、碱金属醇盐或甲醇镁。In the preparation of a liquid or solid dosage form, the active ingredient A can be first dissolved in certain specific basic substances to form a benzisothiazolin metal salt. Suitable basic substances include: alkali metal carbonates, alkali metal hydrogens Oxide (such as sodium hydroxide, potassium hydroxide), alkali metal alkoxy carbonate, alkali metal alkoxide or magnesium methoxide.
本发明的组合物中两种有效成分表现为增效效果，该组合物的活性比使用单个化合物的活性预期总和，以及单个化合物的单独活性更为显著。增效效果表现为允许施用量减少、更宽的杀真菌控制谱、见效快、更持久的防治效果、通过仅仅一次或少数几次施用更好的控制植物有害真菌、以及加宽了可能的施用间隔时间。这些特性是植物真菌控制实践过程中特别需要的。The two active ingredients in the compositions of the present invention exhibit synergistic effects, the activity of which is more pronounced than the expected sum of activity using a single compound, and the individual activity of a single compound. The synergistic effect is manifested by allowing for a reduced application rate, a broader fungicidal control profile, quicker effect, longer lasting control effect, better control of plant harmful fungi by only one or a few applications, and broadening of possible application. Intervals. These properties are particularly desirable in the practice of plant fungi control.
本发明的杀菌剂组合物可应用于农业领域防治农作物病害方面，如番茄早疫病、甜椒白星病、南瓜花叶病毒病、葡萄霜霉病、小麦纹枯病、柑橘炭疽病等,同时本发明也可以防治作物其它病害,包括但不限于小麦病害(如：小麦赤霉病、小麦白粉病、小麦锈病等)、水稻病害(如：水稻纹枯病、水稻稻曲病、水稻稻瘟病、水稻细菌性条斑等)、玉米病害(如：玉米黑穗病、玉米大斑病、玉米小斑病)、黄瓜病害(如：黄瓜霜霉病、黄瓜白粉病、黄瓜炭疽病、黄瓜细菌性角斑病等)、番茄病害(如：番茄炭疽病、番茄灰霉病、番茄细菌性角斑病等)、葡萄病害(如：葡萄灰霉病、葡萄白粉病)、苹果病害(如苹果轮纹病、苹果炭疽病等)、柑橘病害(柑橘溃疡病、柑橘疮痂并)、烟草病害(烟草野火病)等。The fungicide composition of the invention can be applied to the agricultural field for controlling crop diseases, such as tomato early blight, sweet pepper white star disease, pumpkin mosaic virus disease, grape downy mildew, wheat sheath blight, citrus anthracnose, etc. The invention can also control other diseases of crops, including but not limited to wheat diseases (such as wheat scab, wheat powdery mildew, wheat rust, etc.), rice diseases (such as rice sheath blight, rice smut, rice blast, Rice bacterial streaks, etc., corn diseases (such as: corn smut, corn big spot disease, corn small spot disease), cucumber diseases (such as: cucumber downy mildew, cucumber powdery mildew, cucumber anthracnose, cucumber bacterial Angle spot disease, etc., tomato diseases (such as: tomato anthracnose, tomato gray mold, tomato bacterial angular spot disease, etc.), grape diseases (such as: grape gray mold, grape powdery mildew), apple disease (such as apple wheel) Phytophthora, apple anthracnose, etc.), citrus diseases (citrus canker, citrus sores), tobacco diseases (tobacco wildfire).
本发明的杀菌组合物的表现出的其它特点主要表现为：1、本发明的组合物混配具有明显的增效作用；2、由于本组合物的两个单剂化学结构差异很大，作用机理完全不同，不存在交互抗性，可延缓两单剂单独使用所产生的抗性问题；3、本发明的组合物对作物安全、防效好。经试验证明，本发明杀菌剂组合物化学性质稳定，增效显著，对防治对象表现出明显的增效以及互补作用。The other characteristics exhibited by the bactericidal composition of the present invention are mainly as follows: 1. The compounding of the composition of the present invention has obvious synergistic effect; 2. Since the chemical composition of the two single agents of the present composition is greatly different, the effect The mechanism is completely different, there is no cross-resistance, and the problem of resistance caused by the separate use of the two single agents can be delayed; 3. The composition of the present invention is safe and safe for crops. It has been proved by experiments that the bactericidal composition of the invention has stable chemical properties, remarkable synergistic effect, and exhibits obvious synergistic effect and complementary effect on the control object.
具体实施方式 detailed description
为了使本发明的目的、技术方案及优点更加清楚明白，以下结合实施例，对本发明进行进一步详细说明。应当理解，此处所描述的具体实施例仅用以解释本发明，并不用于限定本发明，凡在本发明的精神和原则之内所做的任何修改、等同替换和改进等，均应包含在本发明的保护范围之内。In order to make the objects, technical solutions and advantages of the present invention more comprehensible, the present invention will be further described in detail below with reference to the embodiments. It is understood that the specific embodiments described herein are intended to be illustrative of the invention and are not to be construed as limiting the scope of the invention. Within the scope of protection of the present invention.
以下实施例所有配方中百分比均为重量百分比。本发明组合物各种制剂的加工工艺均为现有技术，根据不同情况可以有所变化。The percentages in all formulations in the following examples are percentages by weight. The processing techniques of the various formulations of the compositions of the present invention are all prior art and may vary depending on the circumstances.
一、剂型制备实施例First, the dosage form preparation example
(一)水分散粒剂的加工及实施例(1) Processing and examples of water-dispersible granules
将活性成分活性分组A与活性组分B，与助剂和填料按配方的比例混合均匀，经气流粉碎成可湿性粉剂，再加入一定量的水混合挤压造粒，经干燥筛分后制得水分散粒剂产品。The active ingredient active group A and the active component B, and the auxiliary agent and the filler are uniformly mixed according to the formula, and are pulverized into a wettable powder by a jet stream, and then added with a certain amount of water to be mixed and extruded, granulated, and dried and sieved. A water dispersible granule product.
(1)活性组分A(BIT)与环丙唑醇制备水分散粒剂(1) Preparation of water-dispersible granules by active component A (BIT) and cyproconazole
实施例1：12％BIT·环丙唑醇水分散粒剂Example 1:12% BIT· cyproconazole water dispersible granules
BIT 10％，环丙唑醇2％，硫酸铵3％，脂肪醇硫酸盐4％，苯磺酸钠5％，白炭黑4％，高岭土补足至100％。BIT 10%, cyproconazole 2%, ammonium sulfate 3%, fatty alcohol sulfate 4%, sodium benzenesulfonate 5%, white carbon black 4%, kaolin to 100%.
实施例2：52％BIT·环丙唑醇水分散粒剂Example 2: 52% BIT· cyproconazole water dispersible granules
BIT 2％，环丙唑醇50％，黄原胶8％，膨润土8％，木质素磺酸钾5％，磺酸钠5％,轻质碳酸钙补足至100％。BIT 2%, cyproconazole 50%, xanthan gum 8%, bentonite 8%, potassium lignosulfonate 5%, sodium sulfonate 5%, light calcium carbonate to 100%.
(2)活性组分A(MBIT)与环丙唑醇制备水分散粒剂(2) Preparation of water-dispersible granules by active component A (MBIT) and cyproconazole
实施例3：12％MBIT·环丙唑醇水分散粒剂Example 3: 12% MBIT· cyproconazole water dispersible granules
MBIT 10％，环丙唑醇2％，其余组分按照实施例1的方法制备。MBIT 10%, cyproconazole 2%, and the remaining components were prepared in accordance with the procedure of Example 1.
实施例4：52％MBIT·环丙唑醇水分散粒剂Example 4: 52% MBIT· cyproconazole water-dispersible granules
MBIT 2％，环丙唑醇50％，其余组分按照实施例2的方法制备。MBIT 2%, cyproconazole 50%, and the remaining components were prepared in the same manner as in Example 2.
(3)活性组分A(BBIT)与环丙唑醇制备水分散粒剂(3) Preparation of water-dispersible granules by active ingredient A (BBIT) and cyproconazole
实施例5：12％BBIT·环丙唑醇水分散粒剂Example 5: 12% BBIT· cyproconazole water dispersible granules
BBIT 10％，环丙唑醇2％，其余组分按照实施例1的方法制备。BBIT 10%, cyproconazole 2%, and the remaining components were prepared in the same manner as in Example 1.
实施例6：52％BBIT·环丙唑醇水分散粒剂Example 6: 52% BBIT· cyproconazole water dispersible granules
BBIT 2％，环丙唑醇50％，其余组分按照实施例2的方法制备。BBIT 2%, cyproconazole 50%, and the remaining components were prepared in accordance with the procedure of Example 2.
(二)悬浮剂的加工及实施例 (2) Processing and examples of suspending agents
将活性成分活性分组A与活性组分B，与分散剂、润湿剂、增稠剂和水等各组分按配方的比例混合均匀，经砂磨和/或高速剪切后，得到半成品，分析后补加水混合均匀过滤即得成品。The active ingredient active group A and the active component B, and the components such as a dispersing agent, a wetting agent, a thickener and water are uniformly mixed according to the formula, and after being sanded and/or sheared at a high speed, a semi-finished product is obtained. After the analysis, the water is mixed and evenly filtered to obtain the finished product.
(1)活性组分A(BIT)与环丙唑醇制备悬浮剂(1) Preparation of suspending agent from active ingredient A (BIT) and cyproconazole
实施例7：11％BIT·环丙唑醇悬浮剂Example 7: 11% BIT· cyproconazole suspending agent
BIT 10％，环丙唑醇1％，脂肪醇硫酸盐4％，甲基萘磺酸钠甲醛缩合物6％，丙酮8％，烷基磺酸盐5％,水补足至100％。BIT 10%, cyproconazole 1%, fatty alcohol sulfate 4%, sodium methylnaphthalene sulfonate formaldehyde condensate 6%, acetone 8%, alkyl sulfonate 5%, water to 100%.
实施例8：50％BIT·环丙唑醇悬浮剂Example 8: 50% BIT· cyproconazole suspension
BIT 25％，环丙唑醇25％，方解石5％，乙醇8％，木质素苯磺酸钾10％，桂酸聚乙二醇醚缩醛10％，水补足至100％。BIT 25%, cyproconazole 25%, calcite 5%, ethanol 8%, lignin potassium sulfonate 10%, lauric acid polyethylene glycol ether acetal 10%, water to 100%.
实施例9：31.5％BIT·环丙唑醇悬浮剂Example 9: 31.5% BIT· cyproconazole suspension
BIT 1.5％，环丙唑醇30％，膨润土6％，苯磺酸钠10％，黄原胶6％，甲苯5％，木质素亚硫酸盐废液8％,水补足至100％。BIT 1.5%, cyproconazole 30%, bentonite 6%, sodium benzene sulfonate 10%, xanthan gum 6%, toluene 5%, lignin sulfite waste 8%, water to 100%.
(2)活性组分A(MBIT)与环丙唑醇制备悬浮剂(2) Preparation of suspending agent from active ingredient A (MBIT) and cyproconazole
实施例10：11％MBIT·环丙唑醇悬浮剂Example 10: 11% MBIT· cyproconazole suspension
MBIT 10％，环丙唑醇1％，其余组分按照实施例7的方法制备。MBIT 10%, cyproconazole 1%, and the remaining components were prepared in accordance with the procedure of Example 7.
实施例11：50％MBIT·环丙唑醇悬浮剂Example 11: 50% MBIT· cyproconazole suspension
MBIT 25％，环丙唑醇25％，其余组分按照实施例8的方法制备。MBIT 25%, cyproconazole 25%, and the remaining components were prepared in accordance with the procedure of Example 8.
实施例12：31.5％MBIT·环丙唑醇悬浮剂Example 12: 31.5% MBIT· cyproconazole suspension
MBIT 1.5％，环丙唑醇30％，其余组分按照实施例9的方法制备。MBIT 1.5%, cyproconazole 30%, and the remaining components were prepared in accordance with the procedure of Example 9.
(3)活性组分A(BBIT)与环丙唑醇制备悬浮剂(3) Preparation of suspending agent from active ingredient A (BBIT) and cyproconazole
实施例13：11％BBIT·环丙唑醇悬浮剂Example 13: 11% BBIT· cyproconazole suspending agent
BBIT 10％，环丙唑醇1％，其余组分按照实施例7的方法制备。BBIT 10%, cyproconazole 1%, and the remaining components were prepared in accordance with the procedure of Example 7.
实施例14：50％BBIT·环丙唑醇悬浮剂Example 14: 50% BBIT· cyproconazole suspension
BBIT 25％，环丙唑醇25％，其余组分按照实施例8的方法制备。BBIT 25%, cyproconazole 25%, and the remaining components were prepared in accordance with the procedure of Example 8.
实施例15：31.5％BBIT·环丙唑醇悬浮剂Example 15: 31.5% BBIT· cyproconazole suspension
BBIT 1.5％，环丙唑醇30％，其余组分按照实施例9的方法制备BBIT 1.5%, cyproconazole 30%, the remaining components were prepared according to the method of Example 9.
(三)可湿性粉剂的加工及实施例(3) Processing and examples of wettable powders
将活性成分A与B活性成分与各种助剂及填料等按比例充分混合，经超细粉碎机粉 碎后制得可湿性粉剂。The active ingredients A and B active ingredients are mixed with various auxiliaries and fillers in proportion, and the ultrafine pulverizer powder is mixed. After being crushed, a wettable powder is obtained.
(1)活性组分A(BIT)与环丙唑醇制备可湿性粉剂(1) Preparation of wettable powder by active ingredient A (BIT) and cyproconazole
实施例16:55％BIT·环丙唑醇可湿性粉剂(1:10)Example 16: 55% BIT· cyproconazole wettable powder (1:10)
BIT 5％，环丙唑醇50％，烷基硫酸盐5％，硫酸铵8％，喷闰土8％，高岭土补足至100％。BIT 5%, cyproconazole 50%, alkyl sulfate 5%, ammonium sulfate 8%, spurted earth 8%, kaolin to 100%.
实施例17:31％BIT·环丙唑醇可湿性粉剂(1:30)Example 17: 31% BIT· cyproconazole wettable powder (1:30)
BIT 1％，环丙唑醇30％，烷基磺酸盐8％，乙氧基化聚氧丙烯8％，黄原胶6％，白炭黑补足至100％。BIT 1%, cyproconazole 30%, alkyl sulfonate 8%, ethoxylated polyoxypropylene 8%, xanthan gum 6%, white carbon black complement to 100%.
(2)活性组分A(MBIT)与环丙唑醇制备可湿性粉剂(2) Preparation of wettable powder by active ingredient A (MBIT) and cyproconazole
实施例18：55％MBIT·环丙唑醇可湿性粉剂Example 18: 55% MBIT· cyproconazole wettable powder
MBIT 5％，环丙唑醇50％，其余组分按照实施例16的方法制备。MBIT was 5%, cyproconazole was 50%, and the remaining components were prepared in the same manner as in Example 16.
实施例19：31％MBIT·环丙唑醇可湿性粉剂Example 19: 31% MBIT· cyproconazole wettable powder
MBIT 1％，环丙唑醇30％，其余组分按照实施例17的方法制备。MBIT 1%, cyproconazole 30%, and the remaining components were prepared in accordance with the procedure of Example 17.
(3)活性组分A(BBIT)与环丙唑醇制备可湿性粉剂(3) Preparation of wettable powder by active ingredient A (BBIT) and cyproconazole
实施例20：55％BBIT·环丙唑醇可湿性粉剂Example 20: 55% BBIT· cyproconazole wettable powder
BBIT 5％，环丙唑醇50％，其余组分按照实施例16的方法制备。BBIT 5%, cyproconazole 50%, and the remaining components were prepared in accordance with the procedure of Example 16.
实施例21：31％BBIT·环丙唑醇可湿性粉剂Example 21: 31% BBIT· cyproconazole wettable powder
BBIT 1％，环丙唑醇30％，其余组分按照实施例17的方法制备。BBIT 1%, cyproconazole 30%, and the remaining components were prepared in accordance with the procedure of Example 17.
二、药效验证试验Second, the efficacy test
(一)生物测定实施例(1) Bioassay examples
按照试验分级标准调查整株叶片的发病情况，计算病情指数和防治效果。According to the test grading standards, the incidence of the whole plant leaves was investigated, and the disease index and control effect were calculated.
将防治效果换算成几率值(y)，药液弄高度(μg/ml)转换成对数值(x)，以最小二乘法计算毒力方程和抑制中浓度EC50，依孙云沛法计算药剂的毒力指数级共毒系数(CTC)。The control effect is converted into the probability value (y), the liquid height (μg/ml) is converted into a logarithmic value (x), the virulence equation is calculated by the least squares method, and the neutral concentration EC50 is suppressed, and the virulence of the drug is calculated according to the method of Sun Yunpei. Exponential Co-toxicity Factor (CTC).
实测毒力指数(ATI)＝(标准药剂EC50/供试药剂EC50)*100Measured virulence index (ATI) = (standard drug EC50 / test drug EC50) * 100
理论毒力指数(TTI)＝A药剂毒力指数*混剂中A的百分含量+B药剂毒力指数*混剂中B的百分含量Theoretical virulence index (TTI) = A virulence index * Percentage of A in the mixture + B virulence index * Percentage of B in the mixture
共毒系数(CTC)＝[混剂实测毒力指数(ATI)/混剂理论毒力指数(TTI)]*100Co-toxicity coefficient (CTC) = [mixture measured virulence index (ATI) / mixed theory virulence index (TTI)] * 100
CTC≤80,组合物表现为拮抗作用,80＜CTC＜120，组合物表现为相加作用,CTC≥120，组合物表现为增效作用。 CTC ≤ 80, the composition showed antagonism, 80 < CTC < 120, the composition showed an additive effect, CTC ≥ 120, and the composition showed synergistic effect.
1、BIT与环丙唑醇复配对番茄早疫病毒力测定试验1. BIT and cyproconazole paired with tomato early virulence virus test
表1. BIT与环丙唑醇复配对番茄早疫病毒力测定结果分析Table 1. Analysis of the results of BIT and cyproterol in pairing with tomato early virulence virus
药剂名称Pharmacy name EC50(μg/ml)EC 50 (μg/ml) ATIATI TTITTI 共毒系数(CTC)Co-toxicity coefficient (CTC)
BITBIT 25.5725.57 100.00100.00 \\ \\
环丙唑醇Cyclopropazole 19.6819.68 129.93129.93 \\ \\
BIT：环丙唑醇＝20:1BIT: cyproconazole = 20:1 20.5720.57 124.33124.33 101.43101.43 122.58122.58
BIT：环丙唑醇＝10:1BIT: cyproconazole = 10:1 19.2319.23 132.97132.97 102.72102.72 129.45129.45
BIT：环丙唑醇＝5:1BIT: cyproconazole = 5:1 17.9117.91 142.81142.81 104.99104.99 136.02136.02
BIT：环丙唑醇＝1:1BIT: cyproconazole = 1:1 15.5715.57 164.22164.22 114.97114.97 142.84142.84
BIT：环丙唑醇＝1:10BIT: cyproconazole = 1:10 13.1313.13 194.77194.77 127.21127.21 153.11153.11
BIT：环丙唑醇＝1:20BIT: cyproconazole = 1:20 14.1514.15 180.66180.66 128.50128.50 140.59140.59
BIT：环丙唑醇＝1:25BIT: cyproconazole = 1:25 14.7914.79 172.91172.91 128.78128.78 134.27134.27
BIT：环丙唑醇＝1:30BIT: cyproconazole = 1:30 15.6215.62 163.69163.69 128.96128.96 126.93126.93
BIT：环丙唑醇＝1:40BIT: cyproconazole = 1:40 16.4916.49 155.05155.05 129.20129.20 120.01120.01
结果(表1)表明，BIT与环丙唑醇复配对番茄早疫病的防治效果显著提高，说明二者复配对番茄早疫病防治有显著的增效作用，尤其是BIT：环丙唑醇＝10～1:1～30范围内,增效效果尤为明显。The results (Table 1) showed that the control effect of BIT and cyproterol on tomato early blight was significantly improved, indicating that there was a significant synergistic effect between the two on the prevention and treatment of tomato early blight, especially BIT: cyproconazole = 10 In the range of 1:1 to 30, the synergistic effect is particularly obvious.
2、MBIT与环丙唑醇复配对甜椒白星病毒力测定试验2, MBIT and cyproterol complex paired sweet pepper white star virus test
表2. MBIT与环丙唑醇复配对甜椒白星病毒力测定结果分析Table 2. Analysis of the results of MBIT and cyproterol complex pairing with sweet pepper white star virus
药剂名称Pharmacy name EC50(μg/ml)EC 50 (μg/ml) ATIATI TTITTI 共毒系数(CTC)Co-toxicity coefficient (CTC)
MBITMBIT 19.7319.73 100.00100.00 \\ \\
环丙唑醇Cyclopropazole 21.4821.48 91.8591.85 \\ \\
MBIT：环丙唑醇＝20:1MBIT: cyproconazole = 20:1 16.9416.94 116.48116.48 99.6199.61 116.93116.93
MBIT：环丙唑醇＝10:1MBIT: cyproconazole = 10:1 16.3716.37 120.55120.55 99.2699.26 121.45121.45
MBIT：环丙唑醇＝5:1MBIT: cyproconazole = 5:1 15.5415.54 126.99126.99 98.6498.64 128.74128.74
MBIT：环丙唑醇＝1:1MBIT: cyproconazole = 1:1 15.1715.17 130.09130.09 95.9395.93 135.62135.62
MBIT：环丙唑醇＝1:10MBIT: cyproconazole = 1:10 14.7514.75 133.72133.72 92.5992.59 144.42144.42
MBIT：环丙唑醇＝1:20MBIT: cyproconazole = 1:20 15.9815.98 123.43123.43 92.2492.24 133.82133.82
MBIT：环丙唑醇＝1:25MBIT: cyproconazole = 1:25 16.8116.81 117.37117.37 92.1692.16 127.35127.35
MBIT：环丙唑醇＝1:30MBIT: cyproconazole = 1:30 17.6717.67 111.64111.64 92.1192.11 121.20121.20
MBIT：环丙唑醇＝1:40MBIT: cyproconazole = 1:40 18.3818.38 107.32107.32 92.0592.05 116.59116.59
结果(表2)表明，MBIT：环丙唑醇＝10～1:1～30范围内,MBIT与环丙唑醇复配对甜椒白星病的防治效果显著提高，说明二者复配对甜椒白星病防治有显著的增效作用。而在以上范围之外，两者之间则表现出相加作用。The results (Table 2) showed that MBIT: cyproconazole = 10 ~ 1:1 ~ 30, the effect of MBIT and cyproterol on the control of sweet pepper white star disease was significantly improved, indicating that the two pairs of sweet pepper white stars Disease prevention and control has a significant synergistic effect. Outside of the above range, the two show an additive effect.
3、BBIT与环丙唑醇对南瓜花叶病毒病毒力测定试验3, BBIT and cyproconazole test for pumpkin mosaic virus
表3. BBIT与环丙唑醇复配对南瓜花叶病毒病毒力测定结果分析Table 3. Analysis of the results of the determination of squash mosaic virus by BBIT and cyproterol
药剂名称Pharmacy name EC50(μg/ml)EC 50 (μg/ml) ATIATI TTITTI 共毒系数(CTC)Co-toxicity coefficient (CTC)
BBITBBIT 15.5515.55 100.00100.00 \\ \\
环丙唑醇Cyclopropazole 9.369.36 166.13166.13 \\ \\
BBIT：环丙唑醇＝20:1BBIT: cyproconazole = 20:1 12.0212.02 129.32129.32 103.15103.15 125.37125.37
BBIT：环丙唑醇＝10:1BBIT: cyproconazole = 10:1 11.1111.11 139.98139.98 106.01106.01 132.04132.04
BBIT：环丙唑醇＝5:1BBIT: cyproconazole = 5:1 9.609.60 161.90161.90 111.02111.02 145.83145.83
BBIT：环丙唑醇＝1:1BBIT: cyproconazole = 1:1 7.667.66 202.88202.88 133.07133.07 152.47152.47
BBIT：环丙唑醇＝1:10BBIT: cyproconazole = 1:10 6.006.00 259.28259.28 160.12160.12 161.93161.93
BBIT：环丙唑醇＝1:20BBIT: cyproconazole = 1:20 6.236.23 249.44249.44 162.98162.98 153.05153.05
BBIT：环丙唑醇＝1:25BBIT: cyproconazole = 1:25 6.506.50 239.20239.20 163.59163.59 146.22146.22
BBIT：环丙唑醇＝1:30BBIT: cyproconazole = 1:30 7.077.07 220.07220.07 164.00164.00 134.19134.19
BBIT：环丙唑醇＝1:40BBIT: cyproconazole = 1:40 7.477.47 208.08208.08 164.52164.52 126.48126.48
结果(表3)表明，尤其是BIT:环丙唑醇＝10～1:1～30范围内,BBIT与环丙唑醇复配对南瓜花叶病毒病的防治效果显著提高，说明二者复配对南瓜花叶病毒病防治有显著的增效作用。The results (Table 3) showed that, especially in the range of BIT: cyproconazole = 10 ~ 1:1 ~ 30, the control effect of BBIT and cyproterol on pumpkin mosaic virus disease was significantly improved, indicating that the two were paired. Pumpkin mosaic virus disease prevention and treatment has a significant synergistic effect.
(二)田间药效验证试验(2) Field efficacy test
试验方法：在发病初期，立即进行第一次喷雾，7天后进行第二次施药，每个处理4个小区，每个小区20平米。于药前和第二次药后11天调查统计发病情况，每个小区5点随机取样，每点调查5株作物，调查整株上每叶片的病斑面积占叶片面积的百分率并分级，计算病情指数和防治效果。Test method: In the early stage of the disease, the first spray was immediately performed, and after 7 days, the second application was carried out, each treatment of 4 cells, 20 square meters per cell. The incidence of the disease was investigated before the drug and 11 days after the second drug. Each plot was randomly sampled at 5 points, and 5 crops were investigated at each point. The percentage of the lesion area per leaf on the whole plant was counted and graded. Disease index and control effect.
Figure PCTCN2017093551-appb-000002
Figure PCTCN2017093551-appb-000002
Figure PCTCN2017093551-appb-000003
Figure PCTCN2017093551-appb-000003
预期防效(％)＝X+Y-XY/100(其中，X，Y为单剂防效)Expected control effect (%) = X + Y-XY / 100 (where X, Y is a single dose control)
分级标准：Grading standards:
0级：无病斑；Level 0: no lesions;
1级：叶片病斑少于5个，长度小于1cm；Grade 1: less than 5 leaf lesions, less than 1 cm in length;
3级：叶片病斑6-10个，部分病斑长度大于1cm；Grade 3: 6-10 leaf lesions, some lesions are longer than 1 cm;
5级：叶片病斑11-25个，部分病斑连成片，病斑面积占叶面积的10-25％；Grade 5: 11-25 leaf lesions, some lesions are connected into pieces, and the lesion area accounts for 10-25% of the leaf area;
7级：叶片病斑26个以上，病斑连成片，病斑面积占叶面积的26-50％；Grade 7: more than 26 leaf lesions, the lesions are connected into pieces, and the lesion area accounts for 26-50% of the leaf area;
9级：病斑连成片，病斑面积占叶面积的50％以上或全叶枯死。Grade 9: The lesions are connected into pieces, and the area of the lesions accounts for more than 50% of the leaf area or the whole leaves are dead.
1、BIT与环丙唑醇复配田间药效实验1. BIT and cyproconazole compound field efficacy experiment
表4 BIT与环丙唑醇混配对葡萄霜霉病防治效果Table 4 BIT and cyproconazole mixed with grape downy mildew control effect
Figure PCTCN2017093551-appb-000004
Figure PCTCN2017093551-appb-000004
Figure PCTCN2017093551-appb-000005
Figure PCTCN2017093551-appb-000005
测定结果(表4)表明，BIT与环丙唑醇的复配对葡萄霜霉病防效明显提高，说明二者复配对葡萄霜霉病有显著的增效作用。The results of the determination (Table 4) showed that the combination of BIT and cyproterol significantly improved the control effect of grape downy mildew, indicating that the two had a significant synergistic effect on grape downy mildew.
2、MBIT与环丙唑醇复配田间药效实验2, MBIT and cyproconazole compound field efficacy experiment
表5 MBIT与环丙唑醇混配对小麦纹枯病防治效果Table 5 MBIT and cyproconazole mixed with wheat sheath blight control effect
Figure PCTCN2017093551-appb-000006
Figure PCTCN2017093551-appb-000006
Figure PCTCN2017093551-appb-000007
Figure PCTCN2017093551-appb-000007
Figure PCTCN2017093551-appb-000008
Figure PCTCN2017093551-appb-000008
测定结果(表5)表明，MBIT与环丙唑醇混配对小麦纹枯病的防效明显提高，说明二者复配对小麦纹枯病有显著的增效作用。The results (Table 5) showed that the control effect of MBIT combined with cyproterone on wheat sheath blight was significantly improved, indicating that the two had a significant synergistic effect on wheat sheath blight.
3、BBIT与环丙唑醇复配田间药效实验3, BBIT and cyproconazole compound field efficacy experiment
表6 BBIT与环丙唑醇混配对柑橘炭疽病防治效果Table 6 BBIT and cyproconazole mixed with citrus anthracnose control effect
Figure PCTCN2017093551-appb-000009
Figure PCTCN2017093551-appb-000009
Figure PCTCN2017093551-appb-000010
Figure PCTCN2017093551-appb-000010
测定结果(表6)表明，BBIT与环丙唑醇混配对柑橘炭疽病的防效明显提高，说明二者复配对柑橘炭疽病有显著的增效作用。 The results of the determination (Table 6) showed that the control effect of BBIT combined with cyproterone on citrus anthracnose was significantly improved, indicating that the two had a significant synergistic effect on citrus anthracnose.

Claims (10)

  1. 一种杀菌剂组合物，其特征在于所述的组合物包含A和B两种活性组分，其中活性组分A为具有式(Ⅰ)的结构化合物，活性组分B为环丙唑醇，两组分之间的重量比为10～1:1～30A bactericidal composition, characterized in that the composition comprises two active components A and B, wherein the active component A is a structural compound having the formula (I), and the active component B is cyproconazole. The weight ratio between the two components is 10 to 1:1 to 30
    Figure PCTCN2017093551-appb-100001
    Figure PCTCN2017093551-appb-100001
    式(Ⅰ)中，R选自H或C1～C8烷基。In the formula (I), R is selected from H or a C 1 - C 8 alkyl group.
  2. 根据权利要求1所述的杀菌剂组合物，其特征在于式(Ⅰ)中，R选自H或C1～C4烷基。The bactericidal composition according to claim 1, wherein in the formula (I), R is selected from H or a C 1 - C 4 alkyl group.
  3. 根据权利要求1所述的杀菌剂组合物，其特征在于式(Ⅰ)中，R优先选自H、-CH3或-C4H9，对应的活性组分A分别为1,2-苯并异噻唑啉-3-酮、2-甲基-1,2-苯并异噻唑啉-3-酮或2-丁基-1,2-苯并异噻唑啉-3-酮。The bactericidal composition according to claim 1, wherein in the formula (I), R is preferably selected from H, -CH 3 or -C 4 H 9 , and the corresponding active component A is 1,2-benzene. Isothiazolin-3-one, 2-methyl-1,2-benzisothiazolin-3-one or 2-butyl-1,2-benzisothiazolin-3-one.
  4. 根据权利要求1所述的杀菌剂组合物，其特征在于活性组分A和活性组分B的重量比为5～1:1～25。The bactericidal composition according to claim 1, wherein the weight ratio of the active component A to the active component B is from 5 to 1:1 to 25.
  5. 根据权利要求1～4中任意一项所述的杀菌剂组合物，其特征在于该组合物由活性成分和农药助剂或辅料制成农药上允许的剂型。The bactericidal composition according to any one of claims 1 to 4, wherein the composition is made into a pesticide-acceptable dosage form from an active ingredient and an agrochemical adjuvant or an auxiliary.
  6. 根据权利要求5所述的杀菌剂组合物，其特征在于该组合物由2～80％重量份的活性组分与98～20％重量份的农药助剂或辅料组成农药上允许的剂型。The bactericidal composition according to claim 5, wherein the composition comprises from 2 to 80% by weight of the active ingredient and from 98 to 20% by weight of the pesticide adjuvant or adjuvant to the pesticide-acceptable dosage form.
  7. 根据权利要求5所述的杀菌剂组合物，其特征在于所述的剂型为可湿性粉剂、悬浮剂或水分散粒剂。The bactericidal composition according to claim 5, wherein the dosage form is a wettable powder, a suspension or a water-dispersible granule.
  8. 根据权利要求5或6所述的杀菌剂组合物，其特征在于所述农药助剂或辅料选自载体、溶剂、分散剂、润湿剂、胶粘剂、增稠剂、粘合剂、表面活性剂或肥料中的一种或几种。The bactericidal composition according to claim 5 or 6, wherein the pesticide adjuvant or adjuvant is selected from the group consisting of a carrier, a solvent, a dispersing agent, a wetting agent, an adhesive, a thickener, a binder, and a surfactant. Or one or more of the fertilizers.
  9. 权利要求1～4中任意一项所述的杀菌剂组合物在农业领域防治农作物病害方面的用途。Use of the bactericide composition according to any one of claims 1 to 4 for controlling crop diseases in the agricultural field.
  10. 权利要求1～4中任意一项所述的杀菌剂组合物在农业领域防治番茄早疫病、甜椒白星病、南瓜花叶病毒病、葡萄霜霉病、小麦纹枯病或柑橘炭疽病方面的用途。 The bactericidal composition according to any one of claims 1 to 4 for controlling tomato early blight, sweet pepper white star disease, pumpkin mosaic virus disease, grape downy mildew, wheat sheath blight or citrus anthracnose in the agricultural field use.
PCT/CN2017/093551 2016-08-31 2017-07-19 Germicide composition WO2018040775A1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
CN201610799725.0A CN106234380A (en) 2016-08-31 2016-08-31 A kind of microbicide compositions
CN201610799725.0 2016-08-31

Publications (1)

Publication Number Publication Date
WO2018040775A1 true WO2018040775A1 (en) 2018-03-08

Family

ID=58080854

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/CN2017/093551 WO2018040775A1 (en) 2016-08-31 2017-07-19 Germicide composition

Country Status (2)

Country Link
CN (1) CN106234380A (en)
WO (1) WO2018040775A1 (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN114391547A (en) * 2022-01-19 2022-04-26 安徽省农业科学院植物保护与农产品质量安全研究所 Seed coating formula for preventing and controlling soybean southern blight and verticillium wilt
CN114794129A (en) * 2021-06-21 2022-07-29 广西壮族自治区亚热带作物研究所（广西亚热带农产品加工研究所） Bactericide for anti-anthracnose breeding
CN115868396A (en) * 2022-12-16 2023-03-31 广西南亚热带农业科学研究所 Ecological seedling raising substrate for macadamia nuts

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN106234380A (en) * 2016-08-31 2016-12-21 江苏辉丰农化股份有限公司 A kind of microbicide compositions
CN106922683A (en) * 2017-03-21 2017-07-07 江苏辉丰农化股份有限公司 Composition pesticide containing BIT and Thidiazuron
CN107787989A (en) * 2017-12-10 2018-03-13 广东中迅农科股份有限公司 A kind of bactericidal composition containing benziothiazolinone and Cyproconazole

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1566104A (en) * 1998-06-10 2005-01-19 拜尔公司 Agents for combating plant pests
CN1566113A (en) * 1998-06-17 2005-01-19 拜尔公司 Agents for controlling plant pests
CN106234380A (en) * 2016-08-31 2016-12-21 江苏辉丰农化股份有限公司 A kind of microbicide compositions

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA2707741C (en) * 2007-06-21 2013-04-30 Rohm And Haas Company Microbicidal composition comprising n-methyl-1,2-benzisothiazolin-3-one and at least one of propiconazole and tebuconazole
CN101984809B (en) * 2010-07-22 2012-11-21 福建诺德生物科技有限责任公司 Oil suspension preparation using resin-based vegetable oil as carrier and preparation method thereof
CN101999372B (en) * 2010-12-14 2015-11-25 陕西西大华特科技实业有限公司 Bactericidal composition containing benziothiazolinone and difenoconazole
CN102172240B (en) * 2011-03-01 2015-09-30 陕西西大华特科技实业有限公司 A kind of bactericidal composition containing benziothiazolinone and methoxy acrylic bactericide
CN105685061A (en) * 2016-02-29 2016-06-22 陕西西大华特科技实业有限公司 Application of benziothiazolinone in preventing and treating potato seed-borne diseases and promoting rooting and germination

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1566104A (en) * 1998-06-10 2005-01-19 拜尔公司 Agents for combating plant pests
CN1566113A (en) * 1998-06-17 2005-01-19 拜尔公司 Agents for controlling plant pests
CN106234380A (en) * 2016-08-31 2016-12-21 江苏辉丰农化股份有限公司 A kind of microbicide compositions

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN114794129A (en) * 2021-06-21 2022-07-29 广西壮族自治区亚热带作物研究所（广西亚热带农产品加工研究所） Bactericide for anti-anthracnose breeding
CN114794129B (en) * 2021-06-21 2023-09-26 广西壮族自治区亚热带作物研究所（广西亚热带农产品加工研究所） Pesticide composition for preventing and treating anthracnose of macadimia nut
CN114391547A (en) * 2022-01-19 2022-04-26 安徽省农业科学院植物保护与农产品质量安全研究所 Seed coating formula for preventing and controlling soybean southern blight and verticillium wilt
CN114391547B (en) * 2022-01-19 2024-04-09 安徽省农业科学院植物保护与农产品质量安全研究所 Seed coating formulation for preventing and controlling soybean southern blight and bacterial wilt
CN115868396A (en) * 2022-12-16 2023-03-31 广西南亚热带农业科学研究所 Ecological seedling raising substrate for macadamia nuts
CN115868396B (en) * 2022-12-16 2024-05-24 广西南亚热带农业科学研究所 Ecological seedling raising substrate for macadimia nuts

Also Published As

Publication number Publication date
CN106234380A (en) 2016-12-21

Similar Documents

Publication Publication Date Title
WO2018040775A1 (en) Germicide composition
EP3210472B1 (en) Synergistic fungicide composition
WO2018059606A1 (en) Bactericidal composition containing benzisothiazolinone and mandipropamid
WO2018086633A1 (en) Bactericide composition including benzisothiazolinone and ethylicin
WO2018157649A1 (en) Microbicide composition containing emodin derivative and benzisothiazolinone
WO2017121019A1 (en) Antimicrobial composition
WO2018086634A1 (en) Composition comprising thidiazuron and alternaria tenuissima activator protein
WO2014180020A1 (en) Sterilization composition with synergism
WO2017185559A1 (en) Anti-microbial composition
WO2018126878A1 (en) Fungicide composition containing benzisothiazolinone and tetraconazole
WO2017206825A1 (en) Weeding composition having synergistic effects
WO2018068773A2 (en) Bactericidal composition containing benzisothiazolinone and alternaria tenuissima activator protein
WO2018024067A1 (en) Fungicide composition
WO2015196951A1 (en) Insecticide and acaricide composition having synergism
WO2018001152A1 (en) Bactericide composition
WO2018006462A1 (en) Fungicidal composition
CN106719646A (en) A kind of microbicide compositions comprising anthraquinone analog compound and methoxy acrylic
CN105211075A (en) Bactericidal composition and application thereof
WO2014032362A1 (en) Use of fungicide composition for preventing rice diseases
WO2018036294A1 (en) Pesticide composition
WO2018068772A1 (en) Bactericidal composition containing benzisothiazolinone and ametoctradin
WO2018040788A1 (en) Germicide composition
WO2018028324A1 (en) Weeding composition having synergistic effects
WO2018054396A1 (en) Bactericide composition
WO2018040764A1 (en) Herbicide composition having synergistic effect

Legal Events

Date Code Title Description
DPE2 Request for preliminary examination filed before expiration of 19th month from priority date (pct application filed from 20040101)
121 Ep: the epo has been informed by wipo that ep was designated in this application

Ref document number: 17845078

Country of ref document: EP

Kind code of ref document: A1

NENP Non-entry into the national phase

Ref country code: DE

122 Ep: pct application non-entry in european phase

Ref document number: 17845078

Country of ref document: EP

Kind code of ref document: A1