WO2007028517A2 - VERWENDUNG VON CNI-OD-FORMULIERUNGEN ZUR BEKÄMPFUNG DER WEIßEN FLIEGE - Google Patents
VERWENDUNG VON CNI-OD-FORMULIERUNGEN ZUR BEKÄMPFUNG DER WEIßEN FLIEGE Download PDFInfo
- Publication number
- WO2007028517A2 WO2007028517A2 PCT/EP2006/008387 EP2006008387W WO2007028517A2 WO 2007028517 A2 WO2007028517 A2 WO 2007028517A2 EP 2006008387 W EP2006008387 W EP 2006008387W WO 2007028517 A2 WO2007028517 A2 WO 2007028517A2
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- WO
- WIPO (PCT)
- Prior art keywords
- oil
- insecticide
- methyl
- formula
- suspension
- Prior art date
Links
- HAZMBVVQRZBZDS-LCYFTJDESA-N Clc1ccc(CN(CCS2)/C2=N/Cl)cn1 Chemical compound Clc1ccc(CN(CCS2)/C2=N/Cl)cn1 HAZMBVVQRZBZDS-LCYFTJDESA-N 0.000 description 1
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
- A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
- A01N25/02—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests containing liquids as carriers, diluents or solvents
- A01N25/04—Dispersions, emulsions, suspoemulsions, suspension concentrates or gels
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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
- A01N51/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds having the sequences of atoms O—N—S, X—O—S, N—N—S, O—N—N or O-halogen, regardless of the number of bonds each atom has and with no atom of these sequences forming part of a heterocyclic ring
Definitions
- pesticides used are, inter alia, those containing insecticides from the neonicotinyl series (e.g., imidacloprid or acetamiprid).
- a corresponding agent is marketed, for example, under the name Confidor® SL 200 by Bayer CropScience (Monheim, Germany).
- the invention therefore relates to the use of suspension concentrates based on oil, containing at least one insecticide from the series of neonicotinyls, for controlling eggs and nymphal stages of the white fly by spray application.
- Formulations suitable for use in the invention contain
- At least one neonicotinyl insecticide at least one neonicotinyl insecticide
- At least one penetration promoter at least one vegetable oil,
- additives from the groups of emulsifiers, antifoaming agents, preservatives, antioxidants, dyes and / or inert fillers.
- Suitable penetration promoters in the present context are all those substances which are usually used to improve the penetration of agrochemical active substances into plants.
- Penetration promoters are in this context defined by the fact that they can penetrate from the aqueous spray mixture and / or from the spray coating into the cuticle of the plant and thereby increase the material mobility (mobility) of active ingredients in the cuticle.
- the method described in the literature can be used to determine this property.
- Suitable formulations are prepared by
- At least one neonicotinyl insecticide at least one neonicotinyl insecticide
- additives from the groups of emulsifiers, antifoams, preservatives, antioxidants, dyes and / or inert fillers
- Insecticides from the series of neonicotinyls can be defined by the following formula (II)
- Het is a heterocycle selected from the following group of heterocycles: 2-chloropyrid-5-yl, 2-methylpyrid-5-yl, 1-oxido-3-pyridino, 2-chloro-1-oxido-5-pyridino, 2 , 3-dichloro-1-oxido-5-pyridino, tetrahydrofuran-3-yl, 5-methyl-tetrahydrofuran-3yl, 2-chlorothiazol-5-yl,
- A is N (R 1 ) (R 2 ) or S (R 2 ),
- R 1 is hydrogen, C r C 6 alkyl, phenyl-C r C 4 alkyl, C 3 -C 6 cycloalkyl, C 2 -C 6 alkenyl or C 2 -C 6 alkynyl, and
- X is N-NO 2 , N-CN or CH-NO 2 ,
- EP-Al-192 606, EP-A2-580 533, EP-A2-376 279, EP-A2-235 725).
- a preferred compound used according to the invention is thiamethoxam.
- Clothianidin has the formula
- Another compound which is preferably used according to the invention is thiacloprid.
- Another compound preferably used according to the invention is dinotefuran.
- Another compound preferably used according to the invention is acetamiprid.
- Acetamiprid has the formula
- Another compound preferably used according to the invention is nitenpyram.
- Nitenpyram has the formula
- Another compound preferably used according to the invention is imidacloprid.
- Imidacloprid has the formula
- a compound particularly preferably used according to the invention is imidacloprid.
- Preferred penetration enhancers are alkanol alkoxylates of the formula
- R is straight-chain or branched alkyl having 4 to 20 carbon atoms
- R ' is H, methyl, ethyl, n-propyl, i-propyl, n-butyl, i-butyl, t-butyl, n-pentyl or n-hexyl,
- AO stands for an ethylene oxide radical, a propylene oxide radical, a butylene oxide radical or mixtures of ethylene oxide and propylene oxide radicals or butylene oxide radicals and
- m stands for numbers from 2 to 30.
- a particularly preferred group of penetration promoters are alkanol alkoxylates of the formula
- n stands for numbers from 2 to 20.
- Another particularly preferred group of penetration promoters are alkanol alkoxylates of the formula Ia
- R stands for branched or unbranched C IO -C H alkyl
- n 6 7, 8, 9 or 10
- R ' is hydrogen, methyl, ethyl, n-propyl, i-propyl, n-butyl, i-butyl, t-butyl, n-pentyl or n-hexyl, in particular hydrogen
- Another particularly preferred group of penetration promoters are alkanol alkoxylates of the formula
- EO stands for -CH 2 -CH 2 -O-
- q stands for numbers from 1 to 10.
- Another particularly preferred group of penetration promoters are alkanol alkoxylates of the formula
- EO stands for -CH 2 -CH 2 -O-
- PO is CH-CH-O ;
- s stands for numbers from 1 to 10.
- Another particularly preferred group of penetration promoters are alkanol alkoxylates of the formula
- EO is CH 2 -CH 2 -O-
- alkanol alkoxylates of the formula
- R and R 1 have the meanings given above,
- BO is - CH ⁇ CH ⁇ TCH-0
- EO is CH 2 -CH 2 -O-
- s stands for numbers from 1 to 10.
- Another particularly preferred group of penetration promoters are alkanol alkoxylates of the formula
- u stands for numbers from 6 to 17.
- R is preferably butyl, isobutyl, n-pentyl, i-pentyl, neopentyl, n-hexyl, i-hexyl, n-octyl, i-octyl, 2-ethylhexyl, nonyl, i-nonyl, decyl, n Dodecyl, i-dodecyl, lauryl, myristyl, i-tridecyl, trimethyl-nonyl, palmityl, stearyl or eicosyl.
- alkanol alkoxylate of the formula (Ia) is the compound of the formula
- R is branched C 1 -C 4 -alkyl
- n 6 (where the number 6 represents an average value)
- R ' is hydrogen
- alkanol alkoxylate of the formula (Ic) is 2-ethyl-hexyl alkoxylate of the formula
- EO stands for -CH 2 -CH 2 -O-
- EO is CH 2 -CH 2 -O-
- alkanol alkoxylate of the formula (If) is the compound (If-I), CH 3 - (CH 2 ) 10> 5-CH 2 O - (- CH 2 -CH 2 -O-) 8j 4-R '(If-I)
- alkanol alkoxylates are generally defined by the above formula (I). These substances are mixtures of substances of the specified type with different chain lengths. For the indices, therefore, average values are calculated, which can also differ from whole numbers.
- alkanol alkoxylates of the formulas given are known or can be prepared by known methods (cf., WO 98-35553, WO 00-35278 and EP-A 0 681 865).
- oils are all commonly used in agrochemical means, recoverable from plants oils in question. Examples include sunflower oil, rapeseed oil, olive oil, castor oil, rapeseed oil, corn kernel oil, cottonseed oil and soybean oil.
- the oil-based suspension concentrates which can be used according to the invention contain at least one nonionic surfactant or dispersing assistant and / or at least one anionic surfactant or dispersing assistant.
- Suitable nonionic surfactants or dispersing agents are all substances of this type which can usually be used in agrochemical compositions.
- Suitable anionic surfactants are all substances of this type conventionally usable in agrochemical compositions. Preference is given to alkali metal and alkaline earth metal salts of alkyl sulfonic acids or alkylaryl sulfonic acids.
- a further preferred group of anionic surfactants or dispersants are salts of polystyrenesulfonic acids which are sparingly soluble in vegetable oil, salts of polyvinylsulfonic acids, salts of naphthalenesulfonic acid-formaldehyde condensation products, salts of condensates. sation products of naphthalenesulfonic acid, phenolsulfonic acid and formaldehyde and salts of lignosulfonic acid.
- Suitable additives which may be present in the formulations which can be used according to the invention are emulsifiers, foam-inhibiting agents, preservatives, antioxidants, dyes and inert fillers.
- Preferred emulsifiers are ethoxylated nonylphenols, reaction products of alkylphenols with ethylene oxide and / or propylene oxide, ethoxylated arylalkylphenols, furthermore ethoxylated and propoxylated arylalkylphenols, and sulfated or phosphated arylalkyl ethoxylates or ethoxy-propoxylates, sorbitan derivatives such as polyethylene oxide sorbitan fatty acid esters and sorbitan Fatty acid esters, may be mentioned as examples.
- Suitable foam-inhibiting substances are all substances customarily usable for this purpose in agrochemical compositions.
- Preferred are silicone oils and magnesium stearate.
- Suitable preservatives are all substances customarily usable for this purpose in agrochemical compositions of this type. Examples which may be mentioned are Preventol® (Bayer AG) and Proxel®.
- antioxidants are all commonly used for this purpose in agrochemical agents substances into consideration. Preference is given to butylhydroxytoluene and / or citric acid.
- Suitable dyes are all substances customarily usable for this purpose in agrochemical compositions. Examples include titanium dioxide, carbon black, zinc oxide and blue pigments as well as permanent red FGR.
- Suitable inert fillers are all substances customarily usable for this purpose in agrochemical compositions which do not function as thickeners. Preference is given to inorganic particles, such as carbonates, silicates and oxides, as well as organic substances, such as urea-formaldehyde condensates. Examples include kaolin, rutile, silicon dioxide, so-called highly disperse silica, silica gels, and natural and synthetic silicates, as well as talc.
- the formulations which can be used according to the invention may contain at least one further active ingredient (insecticides, attractants, sterilants, bactericides, acaricides, nematicides, fungicides, growth-regulating substances or herbicides).
- the insecticides include, for example, phosphoric esters, carbamates, carboxylic esters, chlorinated hydrocarbons, phenylureas, substances produced by microorganisms, among others
- Particularly favorable mixing partners are, for example, the following:
- Azoxystrobin Cyazofamide, Dimoxystrobin, Enestrobin, Famoxadone, Fenamidon, Fluoxastrobin, Kresoximmethyl, Metominostrobin, Orysastrobin, Pyraclostrobin, Picoxystrobin
- Inhibitors of cell wall synthesis Benthiavalicarb, Bialaphos, Dimethomorph, Flumo ⁇ h, Iprovalicarb, Polyoxins, Polyoxorim, Validamycin A
- Carbamates for example Alanycarb, Aldicarb, Aldoxycarb, Allyxycarb, Aminocarb, Bendiocarb, Benfuracarb, Bufencarb, Butacarb, Butocarboxim, Butoxycarboxim, Carbaryl, Carbofuran,
- Carbosulfan cloethocarb, dimetilane, ethiofencarb, fenobucarb, fenothiocarb, formantant, furathiocarb, isoprocarb, metam-sodium, methiocarb, methomyl, metolcarb, oxamyl,
- Pirimicarb promecarb, propoxur, thiodicarb, thiofanox, trimethacarb, XMC, xylylcarb,
- Triazamate Organophosphates for example acephates, azamethiphos, azinphos (-methyl, -ethyl), bromophos-ethyl, bromfenvinfos (-methyl), butathiofos, cadusafos, carbophenothione, chloroethoxyfos, chlorfenvinphos, chloroformes, chlorpyrifos (-methyl / -ethyl), coumaphos, Cyanofephos, cyanophos, chlorfenvinphos, demeton-S-methyl, demeton-S-methylsulphone, dialifos, diazinon, dichlofenthione, dichlorvos / DDVP, dicrotophos, dimethoates, dimethyvinphos, dioxabenzofos, disulphoton, EPN, ethion, ethoprophos, Etrimfos, Famphur, Fenamiphos,
- Pyrethroids for example acrinathrin, allethrin (d-cis-trans, d-trans), beta-cyfluthrin, bifenthrin, biotethrin, bioallethrin-S-cyclopentyl isomer, bioethanomethrin, biopermethrin, bioresmethrin, chlovaporthrin, cis-cypermethrin , Cis-resmethrin, cis-permethrin, clocthrin, cycloprothrin, cyfluthrin, cyhalothrin, cypermethrin (alpha-, beta-, theta-, zeta-), cyphenothrin, deltamethrin, empenthrin (IR isomer), esfenvalerate, etofenprox, fenfluthrin , Fenpropathr
- Oxadiazines for example Indoxacarb
- Acetylcholine receptor agonists / antagonists Chloronicotinyls for example acetamipride, clothianidin, dinotefuran, imidacloprid, nitenpyram, nithiazines, thiacloprid, thiamethoxam
- Acetylcholine receptor modulators are Acetylcholine receptor modulators
- Organochlorines for example, camphechlor, chlordane, endosulfan, gamma-HCH, HCH, heptachlor,
- Fiproles for example, acetoprole, ethiprole, fipronil, pyrafluprole, pyriprole, vaniliprole
- Mectins for example avermectin, emamectin, emamectin benzoate, ivermectin, milbemycin
- Juvenile hormone mimetics for example, diofenolan, epofenonans, fenoxycarb, hydroprene, kinoprenes, methoprenes, pyriproxifen, triprene
- Diacylhydrazines for example chromafenozide, Halofenozide, Methoxyfenozide, Tebufenozide
- Benzoylureas for example bistrifluron, chlorofluazuron, diflubenzuron, fluazuron, flucycloxuron, fenphenoxuron, hexaflumuron, lufenuron, novaluron, noviflumuron, penfluron, teflubenzuron, triflumuron
- Organotin compounds for example azocyclotin, cyhexatin, fenbutatin oxides
- Dinitrophenols for example binapacyrl, dinobutone, dinocap, DNOC
- METI's for example fenazaquin, fenpyroximate, pyrimidifen, pyridaben, tebufenpyrad, tolfenpyrad
- tetronic acids for example spirodiclofen, spiromesifen
- spirotetramat for example, spirotetramat (CAS Reg. No .: 203313-25-1) and 3- (2,5-dimethylphenyl) -8-methoxy-2-oxo-1-azaspiro [4.5] dec-3-ene-4 -yl ethyl carbonate (also known as: Carbonic acid, 3- (2,5-dimethylphenyl) -8-methoxy-2-oxo-1-azaspiro [4.5] dec-3-en-4-yl ethyl ester, CAS Reg. - No .: 382608-10-8)
- Fumigants for example aluminum phosphides, methyl bromides, sulfuryl fluorides
- Food inhibitors for example Cryolite, Flonicamid, Pymetrozine Mite growth inhibitors, for example clofentezine, etoxazole, hexythiazox
- the content of the individual components can be varied within a relatively wide range in the oil-based suspension concentrates which can be used according to the invention. That's how the concentrations are
- penetration promoters generally between 5 and 55% by weight, preferably between 15 and 40% by weight
- vegetable oil in general, between 15 and 55% by weight, preferably between 20 and 50% by weight,
- surfactants or dispersing aids generally between 2.5 and 30 wt .-%, preferably between 5.0 and 25 wt .-% and
- At additives generally between 0 and 25 wt .-%, preferably between 0 and 20 wt .-%.
- the oil-based suspension concentrates according to the invention are prepared in such a way that the components are mixed together in the ratios desired in each case.
- the order in which the ingredients are mixed together is arbitrary. Conveniently, one uses the solid components in a finely ground state. However, it is also possible first to subject the suspension formed after mixing the constituents to a coarse and then to a fine grinding so that the mean particle size is less than 20 ⁇ m. Preference is given to suspension concentrates in which the solid particles have an average particle size of between 1 and 10 ⁇ m.
- the temperatures can be varied in carrying out the method according to the invention in a certain range. It generally works at temperatures between 10 0 C and 60 0 C, preferably between 15 ° C and 40 0 C.
- customary mixing and grinding devices which are used for the production of agrochemical formulations are suitable.
- the oil-based suspension concentrates according to the invention are formulations which remain stable even after prolonged storage at elevated temperatures or in the cold, since no crystal growth is observed. They can be converted by dilution with water into homogeneous spray liquids. The application of these spray liquids is carried out according to the invention by spraying.
- the application rate of the oil-based suspension concentrates according to the invention can be varied within a relatively wide range. It depends on the particular agrochemical active ingredients and their content in the formulations.
- agrochemical active substances in particular from the series of neonicotinyls, can be applied in a particularly advantageous manner to plants and / or their habitat.
- plants are understood as meaning all plants and plant populations, such as desired and undesired wild plants or crop plants (including naturally occurring crop plants).
- Crop plants can be plants which can be obtained by conventional breeding and optimization methods or by biotechnological and genetic engineering methods or combinations of these methods, including the transgenic plants and including the plant varieties which can or can not be protected by plant breeders' rights.
- Plant parts are to be understood as meaning all aboveground and subterranean parts and organs of the plants, such as shoot, leaf, flower and root, examples of which include leaves, needles, stems, stems, flowers, fruiting bodies, fruits and seeds, and roots, tubers and rhizomes.
- the plant parts also include crops and vegetative and generative propagation material, such as cuttings, tubers, rhizomes, offshoots and seeds.
- the treatment according to the invention of the plants and plant parts with the formulations according to the invention is carried out directly or by acting on their environment, habitat or storage space according to the usual treatment methods, e.g. by dipping, spraying, vaporizing, atomizing, spreading, spreading and in propagation material, in particular in seeds, further by single or multi-layer wrapping.
- the agrochemical active ingredients contained develop a better biological activity against all stages of the white fly than when applied in the form of the corresponding conventional formulations.
- Cotton plants (Gossypium hirsutum) infested with eggs and larvae of the white fly (Bemisia tabac ⁇ ) are treated by spraying with a composition of the desired composition and concentration.
- the kill is determined in%. 100% means that all animals have been killed; 0% means that no animals were killed.
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- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (AREA)
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Abstract
Description
Claims
Priority Applications (8)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE502006007118T DE502006007118D1 (de) | 2005-09-09 | 2006-08-26 | VERWENDUNG VON CNI-OD-FORMULIERUNGEN ZUR BEKÄMPFUNG DER WEIßEN FLIEGE |
US12/066,034 US20090163554A1 (en) | 2005-09-09 | 2006-08-26 | Use of CNI-OD Formulations for Controlling White Fly |
MX2008003196A MX2008003196A (es) | 2005-09-09 | 2006-08-26 | Uso de formulaciones de cni-od para combatir la mosca blanca. |
EP06791681A EP1926380B1 (de) | 2005-09-09 | 2006-08-26 | VERWENDUNG VON CNI-OD-FORMULIERUNGEN ZUR BEKÄMPFUNG DER WEIßEN FLIEGE |
AT06791681T ATE469552T1 (de) | 2005-09-09 | 2006-08-26 | VERWENDUNG VON CNI-OD-FORMULIERUNGEN ZUR BEKÄMPFUNG DER WEIßEN FLIEGE |
BRPI0615759-9A BRPI0615759A2 (pt) | 2005-09-09 | 2006-08-26 | uso de formulações cni-od para combater a mosca branca |
AU2006289419A AU2006289419A1 (en) | 2005-09-09 | 2006-08-26 | Use of CNI-OD formulations for controlling white fly |
JP2008529502A JP2009507053A (ja) | 2005-09-09 | 2006-08-26 | コナジラミを制御するためのcni−od調剤の使用 |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE102005042880.0 | 2005-09-09 | ||
DE102005042880A DE102005042880A1 (de) | 2005-09-09 | 2005-09-09 | Verwendung von CNI-OD-Formulierungen zur Bekämpfung der Weißen Fliege |
Publications (2)
Publication Number | Publication Date |
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WO2007028517A2 true WO2007028517A2 (de) | 2007-03-15 |
WO2007028517A3 WO2007028517A3 (de) | 2008-04-03 |
Family
ID=37758651
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/EP2006/008387 WO2007028517A2 (de) | 2005-09-09 | 2006-08-26 | VERWENDUNG VON CNI-OD-FORMULIERUNGEN ZUR BEKÄMPFUNG DER WEIßEN FLIEGE |
Country Status (15)
Country | Link |
---|---|
US (1) | US20090163554A1 (de) |
EP (1) | EP1926380B1 (de) |
JP (1) | JP2009507053A (de) |
KR (1) | KR20080042907A (de) |
CN (1) | CN101287373A (de) |
AT (1) | ATE469552T1 (de) |
AU (1) | AU2006289419A1 (de) |
BR (1) | BRPI0615759A2 (de) |
DE (2) | DE102005042880A1 (de) |
ES (1) | ES2345219T3 (de) |
MX (1) | MX2008003196A (de) |
PT (1) | PT1926380E (de) |
TW (1) | TW200803723A (de) |
WO (1) | WO2007028517A2 (de) |
ZA (1) | ZA200802026B (de) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2008113472A2 (en) * | 2007-03-16 | 2008-09-25 | Syngenta Participations Ag | Improvements in or relating to comestibles |
WO2008155108A2 (en) | 2007-06-19 | 2008-12-24 | Gat Microencapsulation, Ag | Oil suspensions of sulphonylureas and agrochemical combinations |
EP2225940A1 (de) | 2009-03-05 | 2010-09-08 | GAT Microencapsulation AG | Öldispersionen von nAChR-bindenden Neonicotinoiden |
FR2965148A1 (fr) * | 2011-04-28 | 2012-03-30 | Rhodia Operations | Dispersion en milieu apolaire contenant des polymeres semi-cristallins a chaines laterales |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2013054194A1 (en) * | 2011-10-13 | 2013-04-18 | Amril Ag | A formulated solvent composition for pesticide |
NZ631396A (en) * | 2014-09-12 | 2016-03-31 | South Star Fertilizers Ltd | Improvements in and relating to fertiliser and like compositions and the manufacture thereof |
CN112450225A (zh) * | 2019-09-06 | 2021-03-09 | 江苏龙灯化学有限公司 | 一种呋虫胺油悬浮剂及其制备方法和用途 |
CN113749089B (zh) * | 2020-06-02 | 2023-11-03 | 江苏龙灯化学有限公司 | 一种具有改善的稳定性的油分散组合物 |
CN111869673A (zh) * | 2020-06-30 | 2020-11-03 | 南通江山农药化工股份有限公司 | 氯噻啉可分散油剂型杀虫剂、制备方法及其用途 |
Citations (1)
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WO2003000053A1 (de) | 2001-06-21 | 2003-01-03 | Bayer Cropscience Ag | Suspensionskonzentrate auf ölbasis |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
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DE19857963A1 (de) * | 1998-12-16 | 2000-06-21 | Bayer Ag | Agrochemische Formulierungen |
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2005
- 2005-09-09 DE DE102005042880A patent/DE102005042880A1/de not_active Withdrawn
-
2006
- 2006-08-26 MX MX2008003196A patent/MX2008003196A/es active IP Right Grant
- 2006-08-26 EP EP06791681A patent/EP1926380B1/de not_active Not-in-force
- 2006-08-26 AU AU2006289419A patent/AU2006289419A1/en not_active Abandoned
- 2006-08-26 JP JP2008529502A patent/JP2009507053A/ja not_active Withdrawn
- 2006-08-26 CN CNA2006800330471A patent/CN101287373A/zh active Pending
- 2006-08-26 BR BRPI0615759-9A patent/BRPI0615759A2/pt not_active IP Right Cessation
- 2006-08-26 PT PT06791681T patent/PT1926380E/pt unknown
- 2006-08-26 ES ES06791681T patent/ES2345219T3/es active Active
- 2006-08-26 AT AT06791681T patent/ATE469552T1/de active
- 2006-08-26 WO PCT/EP2006/008387 patent/WO2007028517A2/de active Application Filing
- 2006-08-26 US US12/066,034 patent/US20090163554A1/en not_active Abandoned
- 2006-08-26 DE DE502006007118T patent/DE502006007118D1/de active Active
- 2006-08-26 KR KR1020087007572A patent/KR20080042907A/ko not_active Application Discontinuation
- 2006-09-08 TW TW095133129A patent/TW200803723A/zh unknown
-
2008
- 2008-03-04 ZA ZA200802026A patent/ZA200802026B/xx unknown
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2003000053A1 (de) | 2001-06-21 | 2003-01-03 | Bayer Cropscience Ag | Suspensionskonzentrate auf ölbasis |
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BYRNE ET AL.: "Whiteflies: their bionomics, pest status and management", INTERCEPT, 1990, pages 227 - 267 |
BYRNE; BELLOWS, ANNUAL REVIEW OF ENTOMOLOGY, vol. 36, 1991, pages 431 - 457 |
HOROWITZ ET AL., BULLETIN OF ENTOMOLOGICAL RESEARCH, vol. 88, 1988, pages 437 - 442 |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2008113472A2 (en) * | 2007-03-16 | 2008-09-25 | Syngenta Participations Ag | Improvements in or relating to comestibles |
WO2008113472A3 (en) * | 2007-03-16 | 2008-12-11 | Syngenta Participations Ag | Improvements in or relating to comestibles |
WO2008155108A2 (en) | 2007-06-19 | 2008-12-24 | Gat Microencapsulation, Ag | Oil suspensions of sulphonylureas and agrochemical combinations |
EP2225940A1 (de) | 2009-03-05 | 2010-09-08 | GAT Microencapsulation AG | Öldispersionen von nAChR-bindenden Neonicotinoiden |
WO2010099965A2 (en) | 2009-03-05 | 2010-09-10 | Gat Microencapsulation Ag | Oil dispersions of nachr binding neonicotinoids |
FR2965148A1 (fr) * | 2011-04-28 | 2012-03-30 | Rhodia Operations | Dispersion en milieu apolaire contenant des polymeres semi-cristallins a chaines laterales |
Also Published As
Publication number | Publication date |
---|---|
CN101287373A (zh) | 2008-10-15 |
ZA200802026B (en) | 2009-10-28 |
ATE469552T1 (de) | 2010-06-15 |
PT1926380E (pt) | 2010-07-29 |
JP2009507053A (ja) | 2009-02-19 |
EP1926380B1 (de) | 2010-06-02 |
EP1926380A2 (de) | 2008-06-04 |
KR20080042907A (ko) | 2008-05-15 |
TW200803723A (en) | 2008-01-16 |
AU2006289419A1 (en) | 2007-03-15 |
WO2007028517A3 (de) | 2008-04-03 |
MX2008003196A (es) | 2008-03-19 |
ES2345219T3 (es) | 2010-09-17 |
DE102005042880A1 (de) | 2007-03-22 |
DE502006007118D1 (de) | 2010-07-15 |
US20090163554A1 (en) | 2009-06-25 |
BRPI0615759A2 (pt) | 2011-05-24 |
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