WO1997006688A1 - Zusammensetzung mit insektizider wirkung - Google Patents
Zusammensetzung mit insektizider wirkung Download PDFInfo
- Publication number
- WO1997006688A1 WO1997006688A1 PCT/EP1996/003454 EP9603454W WO9706688A1 WO 1997006688 A1 WO1997006688 A1 WO 1997006688A1 EP 9603454 W EP9603454 W EP 9603454W WO 9706688 A1 WO9706688 A1 WO 9706688A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- compositions according
- spp
- insecticidal
- microencapsulated
- transfluthrin
- Prior art date
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
- A01N53/00—Biocides, pest repellants or attractants, or plant growth regulators containing cyclopropane carboxylic acids or derivatives thereof
Definitions
- the present invention relates to a new composition based solely on transfluthrin with an insecticidal action, characterized in that it has an excellent action against flying insects, a good knockdown effect, high expulsion effect and a long-lasting residual action against creeping insects and arachnids by microencapsulating the active ingredient becomes.
- Combinations of insecticides are usually used to successfully control insects and arachnids indoors. Different classes of insecticides are usually combined with one another (W. Behrenz and K. Naumann, crop protection news Bayer, 35, 309 (1982)).
- the object of the present invention was to refrain from combinations of insecticides and to restrict oneself to one active substance, the above-mentioned conditions being met.
- composition which is now described which is characterized in that it contains only one active ingredient and has an excellent action against flying insects, a good knock-down action with expulsion effect and residual action against creeping insects and against arachnids.
- the pests mentioned above include:
- Thysanura e.g. Lepisma saccharina.
- Orthoptera e.g. Blatta orientalis, Periplaneta americana, Leucophaea maderae, Blattella germanica, Acheta domesticus, Gryllotalpa spp.
- Thysanoptera e.g. Hercinothrips femoralis, Thrips tabaci.
- Trialeurodes vaporariorum Aphis gossypii, Brevicoryne brassicae, Cryptomyzus ribis, Aphis fabae, Aphis pomi, Eriosoma lanigerum, Hyalopterus arundinis, Phylloxera vastatrix, Pemphigus spp., Macrosiphum avenae, Myzus spp., Phoropalisumum , Nephotettix cincticeps, Lecanium corni, Saissetia oleae, Laodelphax striatellus, Nilaparvata lugens, Aonidiella aurantii, Aspidiotus hederae, Pseudococcus spp., Psylla spp ..
- Anthonomus spp. Sitophilus spp., Otiorrhynchus sulcatus, Cosmopolites sordidus, Ceuthorrhynchus assimilis, Hypera postica, Dermestes spp., Trogoderma spp., Anthrenus spp., Attagenus spp., Lyctus spp., Meliginusus seneus. Gibbium psylloides, Tribolium spp., Tenebrio molitor, Agriotes spp., Conoderus spp., Melolontha melolontha, Amphimallon solstitialis, Costelytra zealandica. ⁇ ".,”",", PCT / EP96 / 03454 O 97/06688
- Hymenoptera e.g. Diprion spp., Hoplocampa spp., Lasius spp., Monomorium pharaonis, Vespa spp ..
- Acarina e.g. Acarus siro, Argas spp., Ornithodoros spp., Dermanyssus gallinae, Eriophyes ribis, Phyllocoptruta oleivora, Boophilus spp., Rhipicephalus spp., Amblyomma spp., Hyalomma spp., Ixodes spp., Psoroptes 5 spp., Ch spp., Tarsonemus spp., Bryobia praetiosa,
- Acarina e.g. Acarus siro, Argas spp., Ornithodoros spp., Dermanyssus gallinae, Eriophyes ribis, Phyllocoptruta oleivora, Boophilus spp., Rhipicephalus spp., Amblyomma spp., Hyalomm
- composition according to the invention is preferred against flying insects such as mosquitoes, flies, moths but also against creeping, hidden vermin, such as e.g. Scraping or fleas applied at all stages of development. 0 These are driven out of their hiding places (flushing effect) so that they come into contact with the freshly created active substance coverings and are killed. If the cockroaches or fleas are sprayed directly, they quickly fall on their back (knockdown) and cannot recover (mortality). To achieve such an effect, transfluthrin can be used in many different ways
- EC Emulsion concentrates
- EW water-based emulsion concentrates
- WP wettable powders
- transfluthrin may be due to its
- cockroaches or fleas Long-term action to control crawling insects, preferably cockroaches or fleas are used. Depending on the amount of expenditure, a short lasting effect means a duration of action of a few days ( ⁇ 1 week). When used as a residual active ingredient, the preparation also works against all larval stages and adult animals of cockroaches and fleas.
- polyurea capsules By microencapsulating transfluthrin in e.g., polyurea capsules can be obtained from the active ingredient with a short lasting effect, through the control system of the microcapsule, a metered release of active ingredient. With the help of this system, a product with a long-term effect can be made from a short-term drug.
- the non-microencapsulated portion can be EC, EW or undiluted
- Liquid (AL) must be formulated.
- Knockdown effect a good expulsion effect and a high residual effect against creeping insects.
- the ratio between the encapsulated CS active ingredient and the free EW portion can be varied in different proportions depending on the effectiveness.
- CS EW ratios of 100 parts CS: 0.1 are used
- Part EW to 0.1 part CS 100 parts EW.
- the ratio of 10 parts of CS: 0.1 part of EW to 0.1 part of CS: 10 parts of EW is preferably used.
- a ratio of 1 part CS: 10 parts EW to 10 parts CS: 1 part EW is particularly preferred.
- the active ingredient concentration of the use forms can be from 0.0000001 to 95% by weight of active ingredient, preferably between 0.0001 and 1% by weight.
- the transfluthrin microcapsules are produced using the interfacial polymerization process.
- the microcapsule wall consists e.g. made of a polyurea material.
- the capsule wall is formed from a polyisocyanate and a polyfunctional amine at the interface between the organic phase and the aqueous phase.
- the polyisocyanate can be aromatic or aliphatic. It should be at least bifunctional, but can also contain more isocyanate groups.
- Polyisocyanates for microencapsulation are e.g. Toluene diisocyanate, diphenylmethane diisocyanate, phenylene diisocyanate, hexamethylene diisocyanate and 1,6-hexane diisocyanate.
- Multifunctional amines should also be at least bifunctional, e.g. Ethylene diamine, hexamethylene diamine, phenyl endiamine, diethylene triamine and tetraethylene pentamine.
- the organic phase consists of a transfluthrin solution and a polyisocyanate.
- the aqueous phase consists of water and a protective colloid, e.g. PVA (polyvinyl alcohol), PVP (polyvinyl pyrrolidone) etc.
- An oil in water (O ⁇ V) emulsion is produced from the aqueous and organic phase.
- the protective colloid prevents the polyisocyanate from reacting with the water during the emulsification process.
- the polyfunctional amine is then added and, if necessary, polymerizes with the polyisocyanate to increase the temperature to form the polyurea microcapsule.
- An aqueous transfluthrin microcapsule suspension is obtained.
- other polymers can also be used for the microencapsulation of transfluthrin.
- the capsule wall material, the size of the microcapsules and the thickness of the polyurea wall - and thus the release of transfluthrin from the microcapsules - can be adjusted accordingly using the manufacturing parameters.
- Transfluthrin is dissolved in Solvesso 200 ® and this solution is mixed with diphenyl methane diisocyanate.
- the organic phase is obtained.
- An O / W emulsion is produced from the PVA solution and the organic phase at a temperature of 25 ° C. (The Ultra Turrax T50 ® from Janke & Kunkel, IKA Labortechnik in Staufen, for example, is used for this.)
- the size of the emulsion droplets which corresponds to the size of the microcapsules, can be adjusted with the emulsification rate and the duration of the emulsification, eg emulsifying at 7000 rpm for 2 min.
- the diethylenetriamine solution is then added with stirring. It is warmed slowly (within 1-2 hours) to 60 ° C. These 60 ° C are kept under stirring for about 5 hours.
- the polymerization of diphenylmethane diisocyanate and diethylene triamine to give the polyurea microcapsule is then completed.
- the aqueous Kelzan S ® gel with benzyl hemiform is added with stirring.
- the polysaccharide Kelzan S ® a so-called xanthan gum, is a polymeric thickener from Kelco.
- Benzylhemiformal, a formaldehyde releaser, is a preservative from Bayer AG.
- the test was carried out in plastic trays (pricking boxes, type 23, WuH Fernholz GmbH & Co. KG, Meinerzhagen) with the dimensions 40 cm x 60 cm x 6 cm.
- the filter paper laid out on the floor was fixed with "tesa” ® film 4104.
- Talc-coated side walls prevented the cockroaches from escaping.
- the hiding place was placed in the middle of the bowls, in the front third an inverted water-filled weighing jar as a potions and a piece of rusk as food.
- Base plate 1 and ceiling plate 3 of the hiding place consist of with white DD
- Lacquer coated aluminum, side bars 5 and slider 2 made of Teflon. Countersunk screws 4 and wing nuts hold the construction together, whereby the desired hiding depth is set using the slider.
- the structure and dimensions of the hiding place are [Fig. 1]. The hiding height can be varied by exchanging the slider and the side bars.
- the hiding place was transferred to the plastic shell on a talc-coated glass ring (height 5 cm, diameter
- the number of cockroaches driven out was up to 5 minutes. to Treatment in one minute, up to 30 min. at five-minute intervals and after 60 minutes. and determined 24 hours. After 60 min. a 9.5 cm diameter kinked filter disc was placed in the pricking boxes as protection for the expelled cockroaches. Control treatment with an active substance-free dose was carried out in each test.
- the tests are carried out in a fume cupboard in which the suction is to be regulated so that the spray jet is not impaired.
- One cockroach is placed in a wire gauze box with an inside diameter of
- test vessels prepared in this way are clamped on the spray apparatus at an angle of 45 °.
- the area behind and under the gauze test container is lined with absorbent filter paper, which is replaced after each test.
- the spray can is clamped on the spray apparatus so that the spray jet hits the wire gauze perpendicularly.
- the time that has to be sprayed before the can content to be applied can be determined from the can to be tested.
- the can is weighed before and after each test to determine the exact amount applied.
- the animals are transferred to a clean container, provided with a swab and evaluated for knock down according to time and% mortality after certain times. Table 2
- Spray volume 2.4 - 2.8 g can content / cockroach from temperature: 22 ° C at a distance of 60 cm rel. Humidity: 47%
- Test method for testing spray cans for their residual effects against crawling insects
- the treatment is carried out in an extraction chamber in which the suction can be regulated in such a way that there is no impairment of the spray jet of the cans.
- the chapel is lined with filter paper on the floor and on the walls up to a height of 65 cm.
- the most important materials can be treated, in particular glazed and unglazed tiles, PVC panels, lacquered plywood, etc.
- the amount that is sprayed beyond the edges of the documents, the spray loss, was determined in extensive tests with cardboard borders and was approximately 10%.
- the spray can is weighed in order to determine the amount of can applied.
- the amount of can content to be dispensed must be discarded.
- the underlay is taken out of its inclined position and laid flat to prevent the spray coating from running off, especially with non-absorbent underlays and extremely moist spray cans. After the spray coatings have dried, the documents are transferred to the test room.
- the treated documents are filled with 5 cockroaches each, which are held in talcum-coated glass rings (diameter 9.5 cm, height 5.5 cm).
- the floor is tiled with unglazed tiles.
- the desired amount of spray can content is from the outside
- the test animals remain in the rooms for 60 minutes. Then the percentage of animals lying on their back (KD) is determined. All animals are removed from the cages and transferred to insecticide-free, crystal-clear plastic cups. The cups are closed with perforated lids and provided with 10% cotton swabs soaked in 10% sugar solution. After the test animals have been kept in an insecticide-free atmosphere for 24 hours, the mortality is determined.
- Spray quantity 2.4-2.8 g can content / scraping temperature 21 ° C from a distance of 60 cm rel.
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
Description
Claims
Priority Applications (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP9508895A JPH11511151A (ja) | 1995-08-16 | 1996-08-05 | 殺虫作用を示す組成物 |
AU67423/96A AU6742396A (en) | 1995-08-16 | 1996-08-05 | Composition having an insecticidal effect |
EP96927685A EP0845945A1 (de) | 1995-08-16 | 1996-08-05 | Zusammensetzung mit insektizider wirkung |
BR9609903A BR9609903A (pt) | 1995-08-16 | 1996-08-05 | ComposiçÃo inseticidamente ativa |
MXPA/A/1998/001247A MXPA98001247A (en) | 1995-08-16 | 1998-02-13 | Composition with insectic effect |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE19530076A DE19530076A1 (de) | 1995-08-16 | 1995-08-16 | Zusammensetzung mit insektizider Wirkung |
DE19530076.9 | 1995-08-16 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO1997006688A1 true WO1997006688A1 (de) | 1997-02-27 |
Family
ID=7769592
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/EP1996/003454 WO1997006688A1 (de) | 1995-08-16 | 1996-08-05 | Zusammensetzung mit insektizider wirkung |
Country Status (11)
Country | Link |
---|---|
EP (1) | EP0845945A1 (de) |
JP (1) | JPH11511151A (de) |
CN (1) | CN1198658A (de) |
AR (1) | AR004182A1 (de) |
AU (1) | AU6742396A (de) |
BR (1) | BR9609903A (de) |
DE (1) | DE19530076A1 (de) |
SV (1) | SV1996000069A (de) |
TR (1) | TR199800230T2 (de) |
WO (1) | WO1997006688A1 (de) |
ZA (1) | ZA966916B (de) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2012028583A1 (de) | 2010-09-03 | 2012-03-08 | Bayer Cropscience Ag | Deltamethrin enthaltende formulierungen |
WO2017177211A1 (en) * | 2016-04-08 | 2017-10-12 | Battelle Memorial Institute | Encapsulation compositions |
WO2019229060A1 (de) | 2018-05-29 | 2019-12-05 | Bayer Aktiengesellschaft | Mikrokapsel-formulierungen enthaltend transfluthrin als flüchtiges insektizid mit verbesserter wirkung |
WO2021094598A1 (de) * | 2019-11-13 | 2021-05-20 | Jesmond Holding Ag | Kombination von verkapseltem phenothrin und emulgiertem prallethrin |
Families Citing this family (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH11147805A (ja) * | 1997-11-18 | 1999-06-02 | Sumitomo Chem Co Ltd | ゴキブリ忌避剤 |
US6534079B1 (en) * | 1999-06-04 | 2003-03-18 | S. C. Johnson & Son, Inc. | Passive space insect repellant strip |
JP2003073204A (ja) * | 2001-09-05 | 2003-03-12 | Sumitomo Chem Co Ltd | 家屋室内における飛翔性害虫の駆除方法 |
US6635077B2 (en) | 2001-09-07 | 2003-10-21 | S.C. Johnson Home Storage, Inc. | Structure including a film material |
GB0129976D0 (en) * | 2001-12-14 | 2002-02-06 | Mars Inc | Treatment method |
MX370945B (es) * | 2012-11-23 | 2020-01-10 | Bayer Cropscience Ag | Uso de un compuesto que comprende un resto de polifluorobencilo contra plagas resistentes a insecticidas. |
CN103070166B (zh) * | 2012-12-26 | 2015-03-04 | 南通联农农药制剂研究开发有限公司 | 一种微囊悬浮-水乳剂zw及其制备方法 |
ES2759423T3 (es) * | 2013-06-26 | 2020-05-11 | Sumitomo Chemical Co | Microcápsulas para difusión térmica |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2306634A1 (fr) * | 1975-04-09 | 1976-11-05 | Minnesota Mining & Mfg | Compositions insecticides en microcapsules |
EP0238184A1 (de) * | 1986-02-07 | 1987-09-23 | The Wellcome Foundation Limited | Pestizide Mischungen |
GB2187957A (en) * | 1986-03-17 | 1987-09-23 | Sumitomo Chemical Co | Microencapsulated pyrethroid insecticidal and/or acaricidal composition |
EP0279325A2 (de) * | 1987-02-19 | 1988-08-24 | Bayer Ag | (+)1 R-trans-2,2-Dimethyl-3-(2,2-dichlorvinyl)-cyclo-propancarbonsäure-2,3,5,6-tetrafluorbenzylester |
EP0368285A2 (de) * | 1988-11-11 | 1990-05-16 | Sumitomo Chemical Company, Limited | Pestizide Zusammensetzung |
-
1995
- 1995-08-16 DE DE19530076A patent/DE19530076A1/de not_active Withdrawn
-
1996
- 1996-08-05 CN CN96197421A patent/CN1198658A/zh active Pending
- 1996-08-05 WO PCT/EP1996/003454 patent/WO1997006688A1/de not_active Application Discontinuation
- 1996-08-05 BR BR9609903A patent/BR9609903A/pt not_active Application Discontinuation
- 1996-08-05 JP JP9508895A patent/JPH11511151A/ja active Pending
- 1996-08-05 EP EP96927685A patent/EP0845945A1/de not_active Withdrawn
- 1996-08-05 TR TR1998/00230T patent/TR199800230T2/xx unknown
- 1996-08-05 AU AU67423/96A patent/AU6742396A/en not_active Abandoned
- 1996-08-14 AR ARP960103991A patent/AR004182A1/es unknown
- 1996-08-15 SV SV1996000069A patent/SV1996000069A/es unknown
- 1996-08-15 ZA ZA9606916A patent/ZA966916B/xx unknown
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2306634A1 (fr) * | 1975-04-09 | 1976-11-05 | Minnesota Mining & Mfg | Compositions insecticides en microcapsules |
EP0238184A1 (de) * | 1986-02-07 | 1987-09-23 | The Wellcome Foundation Limited | Pestizide Mischungen |
GB2187957A (en) * | 1986-03-17 | 1987-09-23 | Sumitomo Chemical Co | Microencapsulated pyrethroid insecticidal and/or acaricidal composition |
EP0279325A2 (de) * | 1987-02-19 | 1988-08-24 | Bayer Ag | (+)1 R-trans-2,2-Dimethyl-3-(2,2-dichlorvinyl)-cyclo-propancarbonsäure-2,3,5,6-tetrafluorbenzylester |
EP0368285A2 (de) * | 1988-11-11 | 1990-05-16 | Sumitomo Chemical Company, Limited | Pestizide Zusammensetzung |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2012028583A1 (de) | 2010-09-03 | 2012-03-08 | Bayer Cropscience Ag | Deltamethrin enthaltende formulierungen |
WO2017177211A1 (en) * | 2016-04-08 | 2017-10-12 | Battelle Memorial Institute | Encapsulation compositions |
US10952431B2 (en) | 2016-04-08 | 2021-03-23 | Battelle Memorial Institute | Releasable encapsulation compositions |
US11375714B2 (en) | 2016-04-08 | 2022-07-05 | Battelle Memorial Institute | Encapsulation compositions |
WO2019229060A1 (de) | 2018-05-29 | 2019-12-05 | Bayer Aktiengesellschaft | Mikrokapsel-formulierungen enthaltend transfluthrin als flüchtiges insektizid mit verbesserter wirkung |
WO2021094598A1 (de) * | 2019-11-13 | 2021-05-20 | Jesmond Holding Ag | Kombination von verkapseltem phenothrin und emulgiertem prallethrin |
Also Published As
Publication number | Publication date |
---|---|
MX9801247A (es) | 1998-05-31 |
AR004182A1 (es) | 1998-11-04 |
CN1198658A (zh) | 1998-11-11 |
AU6742396A (en) | 1997-03-12 |
BR9609903A (pt) | 1999-05-25 |
DE19530076A1 (de) | 1997-02-20 |
TR199800230T2 (xx) | 1998-07-21 |
EP0845945A1 (de) | 1998-06-10 |
SV1996000069A (es) | 1997-02-17 |
JPH11511151A (ja) | 1999-09-28 |
ZA966916B (en) | 1997-02-20 |
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