DE19709121A1 - Cockroach preparations - Google Patents
Cockroach preparationsInfo
- Publication number
- DE19709121A1 DE19709121A1 DE19709121A DE19709121A DE19709121A1 DE 19709121 A1 DE19709121 A1 DE 19709121A1 DE 19709121 A DE19709121 A DE 19709121A DE 19709121 A DE19709121 A DE 19709121A DE 19709121 A1 DE19709121 A1 DE 19709121A1
- Authority
- DE
- Germany
- Prior art keywords
- combination
- acid
- cockroaches
- carboxylic acids
- acids
- Prior art date
- Legal status (The legal status 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 status listed.)
- Withdrawn
Links
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- 229940013764 fipronil Drugs 0.000 description 1
- 235000013312 flour Nutrition 0.000 description 1
- 239000003205 fragrance Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- RGNPBRKPHBKNKX-UHFFFAOYSA-N hexaflumuron Chemical compound C1=C(Cl)C(OC(F)(F)C(F)F)=C(Cl)C=C1NC(=O)NC(=O)C1=C(F)C=CC=C1F RGNPBRKPHBKNKX-UHFFFAOYSA-N 0.000 description 1
- 235000012907 honey Nutrition 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 229940056881 imidacloprid Drugs 0.000 description 1
- YWTYJOPNNQFBPC-UHFFFAOYSA-N imidacloprid Chemical compound [O-][N+](=O)\N=C1/NCCN1CC1=CC=C(Cl)N=C1 YWTYJOPNNQFBPC-UHFFFAOYSA-N 0.000 description 1
- 238000005470 impregnation Methods 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 239000001023 inorganic pigment Substances 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 238000011835 investigation Methods 0.000 description 1
- 229930014550 juvenile hormone Natural products 0.000 description 1
- 239000002949 juvenile hormone Substances 0.000 description 1
- 150000003633 juvenile hormone derivatives Chemical class 0.000 description 1
- 229930191400 juvenile hormones Natural products 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 229940067606 lecithin Drugs 0.000 description 1
- 229920005610 lignin Polymers 0.000 description 1
- PWPJGUXAGUPAHP-UHFFFAOYSA-N lufenuron Chemical compound C1=C(Cl)C(OC(F)(F)C(C(F)(F)F)F)=CC(Cl)=C1NC(=O)NC(=O)C1=C(F)C=CC=C1F PWPJGUXAGUPAHP-UHFFFAOYSA-N 0.000 description 1
- 229960000521 lufenuron Drugs 0.000 description 1
- 239000004579 marble Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229930002897 methoprene Natural products 0.000 description 1
- 229950003442 methoprene Drugs 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 235000010981 methylcellulose Nutrition 0.000 description 1
- 239000003094 microcapsule Substances 0.000 description 1
- 235000010755 mineral Nutrition 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 229910052901 montmorillonite Inorganic materials 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 235000019198 oils Nutrition 0.000 description 1
- 239000011368 organic material Substances 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
- 238000010422 painting Methods 0.000 description 1
- 229910052625 palygorskite Inorganic materials 0.000 description 1
- 239000006072 paste Substances 0.000 description 1
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- 150000003014 phosphoric acid esters Chemical class 0.000 description 1
- 239000001007 phthalocyanine dye Substances 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000002798 polar solvent Substances 0.000 description 1
- 229920000151 polyglycol Polymers 0.000 description 1
- 239000010695 polyglycol Substances 0.000 description 1
- 239000002861 polymer material Substances 0.000 description 1
- 239000011118 polyvinyl acetate Substances 0.000 description 1
- 229920002689 polyvinyl acetate Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- KWYUFKZDYYNOTN-UHFFFAOYSA-M potassium hydroxide Substances [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 1
- 238000007639 printing Methods 0.000 description 1
- 239000003531 protein hydrolysate Substances 0.000 description 1
- 239000008262 pumice Substances 0.000 description 1
- 150000003219 pyrazolines Chemical class 0.000 description 1
- HYJYGLGUBUDSLJ-UHFFFAOYSA-N pyrethrin Natural products CCC(=O)OC1CC(=C)C2CC3OC3(C)C2C2OC(=O)C(=C)C12 HYJYGLGUBUDSLJ-UHFFFAOYSA-N 0.000 description 1
- 229940070846 pyrethrins Drugs 0.000 description 1
- 239000002728 pyrethroid Substances 0.000 description 1
- 229940015367 pyrethrum Drugs 0.000 description 1
- 239000010453 quartz Substances 0.000 description 1
- 229940108410 resmethrin Drugs 0.000 description 1
- VEMKTZHHVJILDY-FIWHBWSRSA-N resmethrin Chemical compound CC1(C)[C@H](C=C(C)C)C1C(=O)OCC1=COC(CC=2C=CC=CC=2)=C1 VEMKTZHHVJILDY-FIWHBWSRSA-N 0.000 description 1
- 239000011435 rock Substances 0.000 description 1
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- 229910052624 sepiolite Inorganic materials 0.000 description 1
- 235000019355 sepiolite Nutrition 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- HEMHJVSKTPXQMS-UHFFFAOYSA-M sodium hydroxide Substances [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 1
- 235000013599 spices Nutrition 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000004575 stone Substances 0.000 description 1
- 235000000346 sugar Nutrition 0.000 description 1
- 229940124530 sulfonamide Drugs 0.000 description 1
- 150000003456 sulfonamides Chemical class 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 229920002994 synthetic fiber Polymers 0.000 description 1
- 239000004758 synthetic textile Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- CJDWRQLODFKPEL-UHFFFAOYSA-N teflubenzuron Chemical compound FC1=CC=CC(F)=C1C(=O)NC(=O)NC1=CC(Cl)=C(F)C(Cl)=C1F CJDWRQLODFKPEL-UHFFFAOYSA-N 0.000 description 1
- 150000005622 tetraalkylammonium hydroxides Chemical class 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- 125000005208 trialkylammonium group Chemical group 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 239000004563 wettable powder Substances 0.000 description 1
- 239000008096 xylene Substances 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
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing carboxylic groups or thio analogues thereof, directly attached by the carbon atom to a cycloaliphatic ring; Derivatives thereof
-
- 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
- A01N25/002—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 a foodstuff as carrier or diluent, i.e. baits
- A01N25/006—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 a foodstuff as carrier or diluent, i.e. baits insecticidal
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/02—Saturated carboxylic acids or thio analogues thereof; Derivatives thereof
- A01N37/04—Saturated carboxylic acids or thio analogues thereof; Derivatives thereof polybasic
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/10—Aromatic or araliphatic carboxylic acids, or thio analogues thereof; Derivatives thereof
-
- 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
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
- A01N47/28—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N<
- A01N47/36—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N< containing the group >N—CO—N< directly attached to at least one heterocyclic ring; Thio analogues thereof
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Pest Control & Pesticides (AREA)
- Dentistry (AREA)
- Engineering & Computer Science (AREA)
- Plant Pathology (AREA)
- Agronomy & Crop Science (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Insects & Arthropods (AREA)
- Food Science & Technology (AREA)
- Toxicology (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Abstract
Description
Die vorliegende Erfindung betrifft die Verwendung einer neuen Kombination von Carbonsäuren als Lockstoffe zum Einsatz bei der Bekämpfung von Schaben, sowie entsprechende Mittel und Vorrichtungen, die diese Kombination enthalten.The present invention relates to the use of a new combination of Carboxylic acids as attractants for use in the control of cockroaches, as well corresponding means and devices containing this combination.
Die Bekämpfung von Schaben, insbesondere in Haushalten, Lebensmittel verarbei tenden Betrieben, Großküchen, Krankenhäusern, aber auch in Viehstallungen ist aus hygienischen und ästhetischen Gründen von großer Bedeutung. Die Effizienz von me chanischen, biologischen und/oder chemischen Bekämpfungsverfahren kann dadurch erheblich gesteigert werden, daß die zu bekämpfenden Schaben durch geeignete Lockmittel wie Köder, bestimmte Farbanordnungen, Duftstoffe, Pheromono und ähn liches zu den Bekämpfungsvorrichtungen bzw. zu den insektiziden Mitteln gelockt werden.The control of cockroaches, especially in households, processes food out of business, canteen kitchens, hospitals, but also in cattle stalls hygienic and aesthetic reasons of great importance. The efficiency of me mechanical, biological and / or chemical control methods can thereby be significantly increased that the cockroaches to be controlled by suitable Attractants such as bait, certain color schemes, fragrances, pheromono and the like Liches to the control devices and the insecticidal agents will.
Es ist bereits bekannt, Schabenpheromone als Lockstoffe einzusetzen, wobei deren Wirksamkeit nicht immer zu befriedigenden Ergebnissen führte. Es ist weiterhin be kannt, daß im Kot von Schaben, z. B. von Blattella germanica Carbonsäuren enthalten sind, die sowohl als Anlockkomponente als auch als Haltekomponente Schaben dazu veranlassen können, feste Aggregationen zu bilden (M.E. Fuchs et al. Z.ang.Ent. 99 (1985) 499-503). Diese Publikation, in der 57 Carbonsäuren als Schabenkot-Inhalts stoffe beschrieben werden, enthält keine praktisch verwertbaren Vorschläge zur Scha benbekämpfung. In der europäischen Anmeldung EP 588 203 werden in sehr allge meiner Form Mischungen von mindestens 2 Carbonsäuren oder Carbonsäurederivaten beschrieben, die als Schabenlockstoffe eingesetzt werden können. Eine experimentelle Überprüfung der dort beschriebenen Kombination zeigte jedoch nur unzureichende Ergebnisse. Dies führte auch zu einer frühzeitigen Aufgabe dieser Patentanmeldung.It is already known to use cockroach pheromones as attractants, and their Effectiveness did not always lead to satisfactory results. It is still be knows that in the droppings of cockroaches, e.g. B. of Blattella germanica carboxylic acids are cockroaches, both as an attracting component and as a holding component can cause solid aggregations to form (M.E. Fuchs et al. Z.ang.Ent. 99 (1985) 499-503). This publication contains 57 carboxylic acids as cockroach droppings substances are described, contains no practical proposals for the Scha fighting. In European application EP 588 203, in very general my form mixtures of at least 2 carboxylic acids or carboxylic acid derivatives described, which can be used as cockroach attractants. An experimental one Examination of the combination described there, however, showed only inadequate Results. This also led to the early abandonment of this patent application.
Die vorliegende Erfindung betrifft eine ausgewählte Kombination aus wenigstens drei
verschiedenen Carbonsäuren aus der Gruppe I bis VI und ihre Verwendung als Lock
stoffe und Aggregationspheromone zum Einsatz bei der Bekämpfung von Schaben.
Die erfindungsgemäße Kombination enthält mindestens 3, vorzugsweise mindestens 4
und insbesondere 6 Elemente aus der folgenden Gruppe:
The present invention relates to a selected combination of at least three different carboxylic acids from groups I to VI and their use as attractants and aggregation pheromones for use in combating cockroaches. The combination according to the invention contains at least 3, preferably at least 4 and in particular 6 elements from the following group:
Die vorstehenden 6 Carbonsäuren als solche und auch ihre mögliche Verwendung als Lock- und Aggregationspheromone sind bereits bekannt. Überraschenderweise wurde gefunden, daß die spezielle Kombination von mindestens 3, insbesondere von 6 dieser Säuren, eine überadditive Lockwirkung auf Schaben besitzen. Bei der erfindungs gemäßen Kombination können die Säuren (I) bis (VI) als solche oder in Form ihrer Salze oder Mischungen dieser Salze mit freien Carbonsäuren eingesetzt werden. Vorzugsweise werden die freien Säuren verwendet.The above 6 carboxylic acids as such and also their possible use as Lock and aggregation pheromones are already known. Surprisingly found that the special combination of at least 3, especially 6 of these Acids, which have an additive attracting effect on cockroaches. In the invention According to the combination, the acids (I) to (VI) as such or in the form of their Salts or mixtures of these salts with free carboxylic acids are used. The free acids are preferably used.
Als Basen zur Herstellung der jeweiligen Salze der Säuren (I) bis (VI) können alle in der Wirkstoffchemie üblichen Basen verwendet werden. Vorzugsweise seien genannt: Alkali-, Erdalkali-, Ammonium-, Alkylammonium-, Dialkylammonium-, Trialkyl ammonium- oder Tetraalkylammoniumhydroxide, besonders bevorzugt Natrium-, Kalium-, Calcium- oder Ammoniumhydroxid. Besonders hervorgehoben sei Natrium hydroxid.As bases for the preparation of the respective salts of the acids (I) to (VI) all in bases customary in active substance chemistry are used. The following should preferably be mentioned: Alkali, alkaline earth, ammonium, alkylammonium, dialkylammonium, trialkyl ammonium or tetraalkylammonium hydroxides, particularly preferably sodium, Potassium, calcium or ammonium hydroxide. Sodium should be particularly emphasized hydroxide.
Phenylmilchsäure (IV) kann in Form ihres Racemats und auch in Form ihrer D- bzw. L-Enantiomeren oder auch deren Mischungen eingesetzt werden, vorzugsweise in Form ihres Racemates.Phenyllactic acid (IV) can be in the form of its racemate and also in the form of its D- or L-enantiomers or mixtures thereof are used, preferably in Form of their racemate.
Die quantitative Zusammensetzung der erfindungsgemäßen Kombination aus den Carbonsäuren (I) bis (VI) kann über weite Bereiche variiert werden. Jedes Element sollte mindestens mit jeweils 0,1 Gew.-%, vorzugsweise mit mindestens 1 Gew.-%, bezogen auf das Gesamtgewicht aller eingesetzten Carbonsäuren, eingesetzt werden. Besonders bevorzugt sind Kombinationen, die die Carbonsäuren in etwa vergleich baren Gewichtsmengen enthalten, die jeweils um 20%, vorzugsweise maximal 10%, voneinander abweichen können.The quantitative composition of the combination according to the invention from the Carboxylic acids (I) to (VI) can be varied over a wide range. Every element should be at least 0.1% by weight, preferably at least 1% by weight, based on the total weight of all carboxylic acids used. Combinations which roughly compare the carboxylic acids are particularly preferred containable amounts by weight, each by 20%, preferably a maximum of 10%, can differ from each other.
Von besonderem Interesse sind folgende erfindungsgemäße Kombinationen mit
entsprechenden Mischungsverhältnissen (alle Angaben in Gewichtsprozent, bezogen
auf die Summe der eingesetzten Carbonsäuren):
The following combinations according to the invention with corresponding mixing ratios (all figures in percent by weight, based on the sum of the carboxylic acids used) are of particular interest:
Die Carbonsäuren (I) bis (VI) sind als solche bekannt und durch übliche Synthesever fahren zugänglich. Das gleiche gilt auch für ihre erfindungsgemäß einsetzbaren Salze und für die Enantiomeren der Formel (IV).The carboxylic acids (I) to (VI) are known as such and by conventional synthetic ver drive accessible. The same also applies to the salts which can be used according to the invention and for the enantiomers of formula (IV).
Die ausgewählte Kombination der Carbonsäuren kann vorteilhaft bei der Bekämpfung von Schaben, also Insekten der Ordnung Blattariae, insbesondere der Familie Blattellidae (Art: Blattella germanica) und der Familie Blattidae (Arten: Blatta orien talis und Periplaneta americana), aber auch gegen andere Schabenarten eingesetzt werden. Besonders bevorzugt ist ihre Verwendung gegen Blattella germanica.The selected combination of carboxylic acids can be advantageous in combating of cockroaches, insects of the Blattariae order, especially of the family Blattellidae (species: Blattella germanica) and the family Blattidae (species: Blatta orien talis and Periplaneta americana), but also used against other cockroaches will. Their use against Blattella germanica is particularly preferred.
Die erfindungsgemäßen Mischungen beeinflussen dabei das Verhalten der Schaben derart, daß diese sich verstärkt an solchen Orten aufhalten oder solche Orte auf suchen, die mit den erfindungsgemäßen Mischungen behandelt wurden, bzw. solche Mischungen enthalten. Die erfindungsgemäßen Mischungen weisen somit eine phero monähnliche Wirkung auf. Diese tritt bei allen beweglichen Entwicklungsstadien (Larven, Adulte) der Schaben auf. Die erfindungsgemäßen Mischungen können somit ganz allgemein bei der Schabenbekämpfung, unabhängig von der Art der angewen deten Bekämpfungsmethode eingesetzt werden.The mixtures according to the invention influence the behavior of the cockroaches in such a way that they stay in such places or such places looking for, which have been treated with the mixtures according to the invention, or such Mixtures included. The mixtures according to the invention thus have a phero effect similar to mon. This occurs at all agile stages of development (Larvae, adults) the cockroaches. The mixtures according to the invention can thus in general in cockroach control, regardless of the type of application control method.
Sie können bei mechanischen Bekämpfungsverfahren, beispielsweise und vorzugs weise in Schabenklebfallen oder Klebevorrichtungen oder bei biologischen oder che mischen Bekämpfungsverfahren oder bei einer Kombination solcher Bekämpfungsver fahren eingesetzt werden. Bei mechanischen Vorrichtungen können die erfindungs gemäßen Mischungen ganz oder weitflächig oder an diskreten Stellen, z. B. durch Be streichen, Aufsprühen, Imprägnieren, Aufdrucken, gegebenenfalls zusammen mit weiteren wirksamen Mitteln wie Ködermaterialien oder anderen Lockmitteln, synthe tischen und natürlichen Insektiziden usw., aufgebracht werden. Bei biologischen oder chemischen Bekämpfungsverfahren können die erfindungsgemäßen Mischungen mit insektenpathogen wirkenden Organismen (z. B. Viren oder Mikroorganismen) oder den synthetischen oder natürlichen Insektiziden vermischt oder in ausreichender Nähe zu diesen Organismen oder Stoffen vorliegen. Bei einer Kombination mehrerer Be kämpfungsmethoden gilt entsprechendes. You can prefer mechanical control methods, for example and wise in cockroach adhesive traps or adhesive devices or with biological or che mix control methods or a combination of such control methods driving can be used. In mechanical devices, the fiction appropriate mixtures over the whole or over a large area or at discrete locations, e.g. B. by Be painting, spraying, impregnation, printing, if necessary together with other effective agents such as bait materials or other attractants, synthe tables and natural insecticides, etc., are applied. With biological or The mixtures according to the invention can be used for chemical control processes organisms with an insect-pathogenic effect (e.g. viruses or microorganisms) or the synthetic or natural insecticides mixed or in close proximity to these organisms or substances. When combining several Be The same applies to methods of fighting.
Dem Fachmann ist es anhand einfacher Überlegungen oder einfacher Untersuchungen leicht möglich, die für die jeweiligen Verwendungszwecke günstigen Mischungen sowie Anwendungsarten und Mengen zu ermitteln.It is simple for a person skilled in the art based on simple considerations or simple investigations easily possible, the mixtures that are favorable for the respective purposes as well as determining types of application and quantities.
Vorzugsweise werden die erfindungsgemäßen Mischungen in einen Insektizide ent haltenen Festköder oder in ein Insektizide enthaltendes Ködergel oder in Klebefallen eingearbeitet oder in der Nähe des Ködermaterials (z. B. darüber) angebracht. Die Mi schungen können auch in einer Form vorliegen, in der sie über einen längeren Zeit raum freigesetzt werden (Slow release - Formulierungen). Hierzu können sie z. B. in Polymermaterial, Paraffine, Wachse usw. eingearbeitet werden oder mikroverkapselt vorliegen. Als Fallen können die üblichen Vorrichtungen dienen und als Ködermaterial die üblichen fraßattraktiven Mittel. Vorzugsweise werden die erfindungsgemäßen Mi schungen in Mengen von 0,0001 bis 100 mg, bevorzugt von 0,01 bis 20 mg und ganz besonders bevorzugt 0,1 bis 10 mg je Köder oder Falle, z. B. Klebfalle, eingesetzt.The mixtures according to the invention are preferably ent in an insecticide solid bait or bait gel containing insecticides or in sticky traps incorporated or attached near the bait material (e.g. above). The Wed Creations can also be in a form in which they are used over a long period of time are released (slow release formulations). You can do this e.g. B. in Polymer material, paraffins, waxes etc. can be incorporated or microencapsulated available. The usual devices can serve as traps and as bait material the usual food attractive means. Preferably, the Mi in amounts of from 0.0001 to 100 mg, preferably from 0.01 to 20 mg and whole particularly preferably 0.1 to 10 mg per bait or trap, e.g. B. adhesive trap used.
Die erfindungsgemäßen Mischungen können auch mit den üblichen insektizidhaltigen Spritzmitteln gemischt werden. Hierbei können die üblichen Formulierungen (z. B. Emulsions-, wettable powder-, Öl-, Aerosol-, Brausetabletten- oder Mikrokapsel-For mulierungen) verwendet werden, die mit den üblicherweise gebräuchlichen Appli kationsgeräten ausgebracht werden können. Ebenso ist es möglich, die erfindungsge mäßen Mischungen in Mischung mit geeigneten Insektiziden zu streufähigen Stäuben oder Granulaten zu formulieren. Die Aufwandmengen der erfindungsgemäßen Mi schungen liegen vorzugsweise bei 1 bis 500 mg pro m2 und besonders bevorzugt bei 2 bis 200 mg pro m2. Durch die Anwendung der erfindungsgemäßen Mischungen kann die Wirksamkeit von mechanischen Vorrichtungen (z. B. Köderstationen, Klebefallen) sowie insbesondere auch von insektiziden Mitteln erheblich verbessert werden. Teil der vorliegenden Erfindung sind somit auch mechanische Schabenbekämpfungsvor richtungen und Mittel, die die erfindungsgemäßen Mischungen enthalten. Bevorzugte mechanische Vorrichtungen und Mittel sind die üblichen Schabenfallen, die gegebe nenfalls Köder, weitere Lock- oder Fraßstoffe und/oder insektizide Stoffe enthalten sowie Mittel mit einer klebrigen Oberfläche, an denen die Schaben haften bleiben, die gegebenenfalls neben üblichen Träger- und Hilfsstoffen Lock- oder Fraßstoffe und/oder insektizid wirksame Stoffe eine der erfindungsgemäßen Mischungen auf weisen. Hierbei können die erfindungsgemäßen Mischungen in der klebrigen Ober fläche enthalten sein oder in deren unmittelbaren Nähe angebracht sein. In den mecha nischen Vorrichtungen können auch Kombinationen von Fallen und Mittel mit klebriger Oberfläche eingesetzt werden.The mixtures according to the invention can also be mixed with the customary insecticidal spray compositions. Here, the customary formulations (e.g. emulsion, wettable powder, oil, aerosol, effervescent tablet or microcapsule formulations) can be used, which can be applied with the commonly used application devices. It is also possible to formulate the mixtures according to the invention in a mixture with suitable insecticides to form sprinkable dusts or granules. The application rates of the mixtures according to the invention are preferably 1 to 500 mg per m 2 and particularly preferably 2 to 200 mg per m 2 . By using the mixtures according to the invention, the effectiveness of mechanical devices (for example bait stations, adhesive traps) and in particular also of insecticidal agents can be considerably improved. Part of the present invention are thus also mechanical cockroach devices and agents containing the mixtures according to the invention. Preferred mechanical devices and means are the usual cockroach traps, which may also contain bait, other attractants or bulking agents and / or insecticidal substances, and means with a sticky surface to which the cockroaches adhere, which, in addition to the usual carriers and auxiliaries, attract locks. or feed and / or insecticidal substances have one of the mixtures according to the invention. Here, the mixtures according to the invention can be contained in the sticky surface or attached in the immediate vicinity thereof. Combinations of traps and agents with a sticky surface can also be used in the mechanical devices.
Ebenfalls Teil der vorliegenden Erfindung sind Schabenbekämpfungsmittel, welche gegebenenfalls neben den üblichen Träger- und Hilfsstoffen und/oder sonstigen Zu satzstoffen (wie Ködermittel und Lockstoffe) eine der erfindungsgemäßen Mischun gen und wenigstens einen insektizid wirksamen Stoff enthalten, wobei die erfindungs gemäße Mischung mit den übrigen Bestandteilen vermischt sein kann oder in einer separaten Anordnung vorliegt. Diese Mittel können zusätzlich oder statt der insektizid wirksamen Stoffe auch entomopathogene Viren oder Mikroorganismen, die gegen Schaben wirksam sind, enthalten.Also part of the present invention are cockroach control agents, which optionally in addition to the usual carriers and auxiliaries and / or other additives Substances (such as bait and attractants) one of the mixtures according to the invention gene and contain at least one insecticidal substance, the invention appropriate mixture can be mixed with the other ingredients or in one separate arrangement. These agents can be in addition to or instead of insecticidal effective substances also entomopathogenic viruses or microorganisms that fight against Cockroaches are effective included.
Als Insektizide können alle Stoffe verwendet werden, die gegen Schaben wirksam sind, da es zu keiner unerwünschten Wechselwirkung zwischen den arthropodizid wirkenden Mitteln und den erfindungsgemäßen Mischungen kommt.All substances that are effective against cockroaches can be used as insecticides as there is no undesirable interaction between the arthropodicide acting agents and the mixtures according to the invention.
Folgende Stoffklassen seien z. B. genannt: Phosphorsäureester, Carbamate, natürliche Pyrethrine, synthetische Pyrethroide, Amidinohydrazone, Sulfluramide, Sulfonamide, Nitroamino-, Nitromethylen-, Cyanoamino-, Cyanomethylenverbindungen, Pyrrolido- 2,4-dion-Derivate, Pyrazolinderivate, Azadirachtine, Annonine und/oder Ryanodine, Avermectine, Ivermectine und verwandte Strukturen.The following classes of substances B. called: phosphoric acid esters, carbamates, natural Pyrethrins, synthetic pyrethroids, amidinohydrazones, sulfluramides, sulfonamides, Nitroamino, nitromethylene, cyanoamino, cyanomethylene compounds, pyrrolido- 2,4-dione derivatives, pyrazoline derivatives, azadirachtine, annonine and / or ryanodine, Avermectins, ivermectins and related structures.
Genauso können Chitinsynthesehemmer (z. B. Triflumuron, Diflubenzuron, Lufen uron, Flufenoxuron), aber auch Juvenilhormone und deren mimetika (z. B. Metho prene, Hydroprene, Fenoxycarb, Pyriproxyfen) oder "Hausmittel" (z. B. Borax, Hefe, Backpulver) verwendet werden. Chitin synthesis inhibitors (e.g. triflumuron, diflubenzuron, lufen) can also be used uron, flufenoxuron), but also juvenile hormones and their mimetics (e.g. metho prene, hydroprene, fenoxycarb, pyriproxyfen) or "home remedies" (e.g. borax, yeast, Baking powder) can be used.
Als erfindungsgemäß verwendbare Insektizide seien beispielhaft und bevorzugt fol gende Wirkstoffe genannt: Abamectin, Betacyfluthrin, Bioresmethrin, Borax, Bor säure, Chlorpyrifos, Cyfluthrin, Cypermethrin, Deltamethrin, Diazinon, Diflubenz uron, Fenitrothion, Fenoxycarb, Fipronil, Flufenoxuron, Hexaflumuron, Hydroprene, Hydramethylnon, Imidacloprid, Lufenuron, Propoxur, Pyrethrum, Pyriproxyfen, Res methrin, Sulfluramid, Teflubenzuron und Triflumuron.Examples of insecticides which can be used according to the invention are, and are preferably fol called active ingredients: Abamectin, Betacyfluthrin, Bioresmethrin, Borax, Bor acid, chlorpyrifos, cyfluthrin, cypermethrin, deltamethrin, diazinon, diflubenz uron, fenitrothion, fenoxycarb, fipronil, flufenoxuron, hexaflumuron, hydroprene, Hydramethylnon, imidacloprid, lufenuron, propoxur, pyrethrum, pyriproxyfen, res methrin, sulfluramide, teflubenzuron and triflumuron.
Die erfindungsgemäßen Kombinationen zur Bekämpfung von Schaben können in übli chen Formulierungen eingesetzt werden, die zusätzlich ein oder mehrere Insektizide in Abhängigkeit von deren jeweiligen physikalischen und/oder chemischen Eigenschaften enthalten können. Als übliche Formulierungen seien beispielsweise genannt: Lösun gen, Emulsionen, Suspensionen, Pulver, Schäume, Pasten, Granulate, Aerosole, Wirk stoff-imprägnierte Natur- und synthetische Stoffe sowie Verkapselungen in polymeren Stoffen.The combinations for combating cockroaches according to the invention can in übli Chen formulations are used, which in addition one or more insecticides Dependence on their respective physical and / or chemical properties can contain. Examples of typical formulations are: solution gen, emulsions, suspensions, powders, foams, pastes, granules, aerosols, active fabric-impregnated natural and synthetic fabrics as well as encapsulations in polymers Fabrics.
Diese Formulierungen werden in bekannter Weise hergestellt, z. B. durch Vermischen der Wirkstoffe mit Hilfs- und/oder Streckmitteln, also flüssigen Lösungsmitteln und/oder festen Trägerstoffen, gegebenenfalls unter Verwendung von oberflächenakti ven Mitteln, also Emulgiermitteln und/oder Dispergiermitteln und/oder schaumerzeu genden Mitteln. Im Falle der Verwendung von Wasser als Streckmittel können z. B. auch organische Lösungsmittel als Hilfslösungsmittel verwendet werden. Als flüssige Lösungsmittel kommen im wesentlichen in Frage: Aromaten wie Xylol, Toluol oder Alkylnaphthaline, chlorierte Aromaten der chlorierten aliphatische Kohlenwasserstoffe wie Chlorbenzole, Chlorethylene oder Methylenchlorid, aliphatische Kohlenwasser stoffe wie Cyclohexan oder Paraffine, z. B. Erdölfraktionen, Alkohole wie Butanol oder Glycol sowie deren Ether und Ester, Ketone wie Aceton, Methylethylketon, Methylisobutylketon oder Cyclohexanon, stark polare Lösungsmittel wie Dimethyl formamid, Dimethylsulfoxid, sowie Wasser.These formulations are prepared in a known manner, e.g. B. by mixing of the active ingredients with auxiliaries and / or extenders, that is to say liquid solvents and / or solid carriers, optionally using surface active agents ve agents, ie emulsifiers and / or dispersants and / or foam generators resources. In the case of the use of water as an extender, e.g. B. organic solvents can also be used as auxiliary solvents. As a liquid Solvents are essentially possible: aromatics such as xylene, toluene or Alkylnaphthalenes, chlorinated aromatics of chlorinated aliphatic hydrocarbons such as chlorobenzenes, chlorethylenes or methylene chloride, aliphatic hydrocarbons substances such as cyclohexane or paraffins, e.g. B. petroleum fractions, alcohols such as butanol or glycol and their ethers and esters, ketones such as acetone, methyl ethyl ketone, Methyl isobutyl ketone or cyclohexanone, strongly polar solvents such as dimethyl formamide, dimethyl sulfoxide, and water.
Als feste Trägerstoffe seien genannt: z. B. natürliche Gesteinsmehle wie Kaoline, Tonerden, Talkum, Kreide, Quarz, Attapulgit, Montmorillonit oder Diatomeenerde und synthetische Gesteinsmehle wie hochdisperse Kieselsäure, Aluminiumoxid und Silikate. Als feste Trägerstoffe für Granulate kommen in Frage: z. B. gebrochene und fraktionierte natürliche Gesteine wie Calcit, Marmor, Bims, Sepiolith, Dolomit, sowie synthetische Granulate aus anorganischen und organischen Mehlen sowie Granulate aus organischem Material wie z. B. Sägemehl, Kokosnußschalen, Maiskolben und Tabakstengel.The following may be mentioned as solid carriers: B. natural stone powder such as kaolins, Clay, talc, chalk, quartz, attapulgite, montmorillonite or diatomaceous earth and synthetic stone powder such as finely divided silica, aluminum oxide and Silicates. Possible solid carriers for granules are: B. broken and fractionated natural rocks such as calcite, marble, pumice, sepiolite, dolomite, as well synthetic granules from inorganic and organic flours as well as granules made of organic material such as B. sawdust, coconut shells, corn cobs and Tobacco stem.
Als Emulgier- und/oder schaumerzeugende Mittel kommen in Frage: z. B. nicht iono gene und anionische Emulgatoren wie Polyoxyethylen-Fettsäure-Ester, Polyoxy ethylen-Fettalkoholether, z. B. Alkylarylpolyglycolether, Alkylsulfonate, Alkylsulfate, Arylsulfonate, sowie Eiweißhydrolisate.Suitable emulsifying and / or foam-generating agents are: B. not iono gene and anionic emulsifiers such as polyoxyethylene fatty acid esters, polyoxy ethylene fatty alcohol ether, e.g. B. alkylaryl polyglycol ethers, alkyl sulfonates, alkyl sulfates, Aryl sulfonates and protein hydrolyzates.
Als Dispergiermittel kommen in Frage: z. B. Lignin-Sulfitablaugen und Methyl cellulose.Possible dispersants are: B. lignin sulfite and methyl cellulose.
Es können in den Formulierungen Haftmittel wie z. B. Carboxymethylcellulose, natür liche und synthetische, pulverige, körnige oder latexförmige Polymere verwendet werden wie z. B. Gummiarabicum, Polyvinylalkohol, Polyvinylacetat als auch natür liche Phospholipide wie z. B. Kephaline und Lecithine und synthetische Phospholipide.Adhesives such as e.g. B. carboxymethyl cellulose, natural Liche and synthetic, powdery, granular or latex-shaped polymers used be like B. gum arabic, polyvinyl alcohol, polyvinyl acetate as well as natural Liche phospholipids such. B. cephalins and lecithins and synthetic phospholipids.
Weitere Additive können z. B. mineralische und vegetabile Öle sein.Other additives can e.g. B. mineral and vegetable oils.
Zusätzlich können anorganische Pigmente, z. B. Eisenoxid, Titanoxid, Ferrocyanblau sowie organische Farbstoffe, z. B. Alizarin-, Azo- und Metallphthalocyaninfarbstoffe verwendet werden.In addition, inorganic pigments, e.g. B. iron oxide, titanium oxide, ferrocyan blue as well as organic dyes, e.g. B. alizarin, azo and metal phthalocyanine dyes be used.
Die Formulierungen enthalten vorzugsweise 0,001 bis 95, insbesondere 0,01 bis 80 Gewichtsprozente der erfindungsgemäßen Kombination und besonders bevorzugt zu sätzlich zwischen 0,1 und 30, insbesondere 0,5 und 15 Gewichtsprozente insektizide Stoffe.The formulations preferably contain 0.001 to 95, in particular 0.01 to 80 Percentages by weight of the combination according to the invention and particularly preferably additionally between 0.1 and 30, in particular 0.5 and 15 percent by weight of insecticides Fabrics.
Die biologische Wirksamkeit der erfindungsgemäßen Mischungen zur Bekämpfung von Schaben soll anhand der folgenden Beispiele erläutert werden.The biological effectiveness of the mixtures according to the invention for combating von Schaben will be explained using the following examples.
8-12 Larven von Blattella germanica im L1-Stadium werden 8 Minuten bei -7°C immobilisiert und in ein Glasgefäß von 9 cm Höhe und 7 cm Durchmesser gegeben. In diesem befinden sich zwei 1,5×3 cm große um 90° quergeknickte Filterpapierstrei fen, die mit der offenen Seite zueinander senkrecht aufgestellt sind. Eines der Papiere war zuvor mit 0,5 ml gelöster Testkombination, das andere nur mit Lösungsmittel be handelt worden.8-12 larvae of Blattella germanica in the L1 stage are kept at -7 ° C for 8 minutes immobilized and placed in a glass jar 9 cm high and 7 cm in diameter. In There are two 1.5 × 3 cm large strips of filter paper folded 90 ° across fen, which are set up perpendicular to each other with the open side. One of the papers was previously with 0.5 ml dissolved test combination, the other only with solvent has been acted.
Das Glas wird mit einem Deckel verschlossen und in einen Wärmeschrank (25°C) gestellt. Nach einer Stunde wird ausgezählt, wieviele Larven sich auf dem Test- und auf dem Kontrollpapier befinden.The glass is closed with a lid and placed in a heating cabinet (25 ° C) posed. After an hour it is counted how many larvae are on the test and on the control paper.
Nach jedem Test wird die Aggregationszahl AZ nach folgender Formel berechnet:
After each test, the aggregation number AZ is calculated using the following formula:
AZ = +10: alle Larven auf Probe
AZ = -10: alle Larven auf Kontrolle
AZ = 0: alle Larven gleichmäßig verteiltAZ = +10: all larvae on sample
AZ = -10: all larvae on control
AZ = 0: all larvae evenly distributed
Insgesamt werden 10 Versuchsglieder angelegt. A total of 10 test elements are created.
Tabelle der ErgebnisseTable of results
0,5% Chlorpyrifos in einer Mischung aus tierischen Fetten, Zucker, Getreide, Lecithin, Honig, Gewürzen mit und ohne erfindungsgemäße Kombination gemäß Beispiel A (Gesamtmenge ca. 3 g).0.5% chlorpyrifos in a mixture of animal fats, sugar, cereals, Lecithin, honey, spices with and without the combination according to the invention Example A (total amount approx. 3 g).
Es werden adulte Männchen der Art Blattella germanica verwendet.Adult males of the species Blattella germanica are used.
Ein Kunststoffbehälter, Boden mit aufgerauhter Glasscheibe versehen (49×59 cm, Höhe 19,5 cm) mit einer Elektrobarriere rund um den oberen Bereich der Innenwände zur Verhinderung des Entkommens von Tieren wird gemäß Abb. 1 eingerichtet.A plastic container, the bottom with a roughened glass pane (49 × 59 cm, height 19.5 cm) with an electrical barrier around the upper area of the inner walls to prevent the escape of animals is set up as shown in Fig. 1.
Zu Versuchsbeginn werden 20 Schaben unter Kohlendioxid betäubt und in das Versteck (V) gegeben, in welchem sich die Rohformulierung als Futterquelle (F) be findet. Nach ca. Stunden wird den auf die unbehandelte Formulierung konditionierten Schaben nun Gelegenheit gegeben, das Versteck zu verlassen. Die unbehandelte Formulierung bleibt im Versteck.At the start of the experiment, 20 cockroaches are stunned under carbon dioxide and into the Given hiding place (V), in which the raw formulation as feed source (F) be finds. After about hours, the is conditioned on the untreated formulation Cockroaches are now given the opportunity to leave the hiding place. The untreated The wording remains in hiding.
Am nächsten Tag wird die Insektizid enthaltende Formulierung (K) in den Kunst stoffbehälter plaziert und jeweils nach 1, 2, 3 und 6 Tagen die prozentuale Mortali tätsrate der Tiere (kumulierend) bestimmt. Tote Tiere werden nicht entfernt. Aus jeweils sechs Versuchen wird der Mittelwert der Mortalität berechnet, wobei der höchste und der niedrigste Wert nicht in die Berechnung einbezogen werden.The next day, the formulation containing insecticide (K) is in art Placed the fabric container and the percentage Mortali after 1, 2, 3 and 6 days activity rate of the animals (cumulative) determined. Dead animals are not removed. Out The average mortality is calculated six times, with the the highest and the lowest value are not included in the calculation.
Erfindungsgemäßes Beispiel A wird separat vom Köder angeboten (aufgetragen auf
Pappblättchen dicht oberhalb des Köders angebracht).
Example A according to the invention is offered separately from the bait (applied to cardboard sheets just above the bait).
Claims (6)
Priority Applications (7)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19709121A DE19709121A1 (en) | 1997-03-06 | 1997-03-06 | Cockroach preparations |
| PCT/EP1998/001019 WO1998038860A1 (en) | 1997-03-06 | 1998-02-23 | Agents for controlling cockroaches |
| AU68224/98A AU6822498A (en) | 1997-03-06 | 1998-02-23 | Agents for controlling cockroaches |
| EP98913576A EP0973387A1 (en) | 1997-03-06 | 1998-02-23 | Agents for controlling cockroaches |
| JP53811098A JP2001513789A (en) | 1997-03-06 | 1998-02-23 | Cockroach growth inhibitor |
| ZA981864A ZA981864B (en) | 1997-03-06 | 1998-03-05 | Composition for controlling cockroaches |
| ARP980100986A AR011181A1 (en) | 1997-03-06 | 1998-03-05 | USE OF A COMBINATION OF AT LEAST 3 CARBOXYLIC ACIDS FOR THE FIGHT AGAINST COCKROACHES AND AGENT FOR THE FIGHT AGAINST COCKROACHES CONTAINING SUCH COMBINATION |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19709121A DE19709121A1 (en) | 1997-03-06 | 1997-03-06 | Cockroach preparations |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE19709121A1 true DE19709121A1 (en) | 1998-09-10 |
Family
ID=7822414
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE19709121A Withdrawn DE19709121A1 (en) | 1997-03-06 | 1997-03-06 | Cockroach preparations |
Country Status (7)
| Country | Link |
|---|---|
| EP (1) | EP0973387A1 (en) |
| JP (1) | JP2001513789A (en) |
| AR (1) | AR011181A1 (en) |
| AU (1) | AU6822498A (en) |
| DE (1) | DE19709121A1 (en) |
| WO (1) | WO1998038860A1 (en) |
| ZA (1) | ZA981864B (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP2140764A1 (en) | 2008-07-03 | 2010-01-06 | Wageningen Universiteit | Behaviour modifying compounds for malaria mosquitoes |
| WO2012010509A3 (en) * | 2010-07-20 | 2012-03-29 | Bayer Cropscience Ag | Gel bait for controlling crawling harmful insects |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP5335765B2 (en) * | 2010-12-17 | 2013-11-06 | 信越化学工業株式会社 | Pesticide sustained-release pheromone formulation with carboxylic acid as pheromone substance |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DD300745A7 (en) * | 1989-08-25 | 1992-07-23 | Ve Kom Ind Tierproduktion | PHEROMON-FRASSGIFT-KOEDER and process for its preparation |
| DE4231281A1 (en) * | 1992-09-18 | 1994-03-24 | Bayer Ag | Cockroach control methods and cockroach control means |
-
1997
- 1997-03-06 DE DE19709121A patent/DE19709121A1/en not_active Withdrawn
-
1998
- 1998-02-23 JP JP53811098A patent/JP2001513789A/en active Pending
- 1998-02-23 AU AU68224/98A patent/AU6822498A/en not_active Abandoned
- 1998-02-23 WO PCT/EP1998/001019 patent/WO1998038860A1/en not_active Ceased
- 1998-02-23 EP EP98913576A patent/EP0973387A1/en not_active Ceased
- 1998-03-05 AR ARP980100986A patent/AR011181A1/en unknown
- 1998-03-05 ZA ZA981864A patent/ZA981864B/en unknown
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP2140764A1 (en) | 2008-07-03 | 2010-01-06 | Wageningen Universiteit | Behaviour modifying compounds for malaria mosquitoes |
| WO2012010509A3 (en) * | 2010-07-20 | 2012-03-29 | Bayer Cropscience Ag | Gel bait for controlling crawling harmful insects |
| CN103025156A (en) * | 2010-07-20 | 2013-04-03 | 拜耳知识产权有限责任公司 | Gel bait for controlling crawling harmful insects |
| CN103025156B (en) * | 2010-07-20 | 2015-08-26 | 拜耳知识产权有限责任公司 | For preventing and treating the gel bait of the harmful insect that creeps |
| RU2572758C2 (en) * | 2010-07-20 | 2016-01-20 | Байер Интеллектуэль Проперти Гмбх | Gel bait for control of crawling insect pests |
Also Published As
| Publication number | Publication date |
|---|---|
| AR011181A1 (en) | 2000-08-02 |
| JP2001513789A (en) | 2001-09-04 |
| EP0973387A1 (en) | 2000-01-26 |
| AU6822498A (en) | 1998-09-22 |
| ZA981864B (en) | 1998-09-08 |
| WO1998038860A1 (en) | 1998-09-11 |
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