WO2005004602A1 - 殺虫殺卵組成物 - Google Patents
殺虫殺卵組成物 Download PDFInfo
- Publication number
- WO2005004602A1 WO2005004602A1 PCT/JP2004/009802 JP2004009802W WO2005004602A1 WO 2005004602 A1 WO2005004602 A1 WO 2005004602A1 JP 2004009802 W JP2004009802 W JP 2004009802W WO 2005004602 A1 WO2005004602 A1 WO 2005004602A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- fatty acids
- insecticidal
- carbon atoms
- ovicidal
- fatty acid
- 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.)
- Ceased
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
- 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
-
- 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
- A01N37/06—Unsaturated 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
- A01N65/00—Biocides, pest repellants or attractants, or plant growth regulators containing material from algae, lichens, bryophyta, multi-cellular fungi or plants, or extracts thereof
- A01N65/40—Liliopsida [monocotyledons]
Definitions
- the present invention relates to an insecticidal and ovicidal composition and an insecticidal and ovicidal method.
- Patent Document 1 discloses a sterilizing composition comprising a phospholipid and an edible oil.
- Patent Document 2 discloses a miticide composed of animal and vegetable fats and oils and a surfactant.
- Patent Document 3 discloses an insecticidal fungicidal composition comprising a medium-chain fatty acid tridalicelide having 8 to 10 carbon atoms and a surfactant.
- Patent Literature 4 discloses an insecticidal composition comprising a medium-chain fatty acid dalyceride and a toxin produced by Bacillus styrogensis bacteria. Further, Patent Document 5 discloses an insecticidal acaricide containing diglycerin monoolate.
- these conventional insecticidal compositions are mainly intended for controlling adults and larvae, and do not reduce or inhibit the hatching ability of insect pest eggs. Therefore, even if such an insecticidal composition is sprayed to control adults and larvae, the hatching ability of eggs already laid in crops and soil is maintained, and as a result, these eggs will eventually hatch. Therefore, it was necessary to spray the insecticidal composition again because the larvae and adults became larvae.
- Patent Document 1 JP-A-53-47532
- Patent Document 2 JP-A-56-140911
- Patent document 3 JP-A-11-29411
- Patent Document 4 JP 2001-64103A
- Patent Document 5 JP-A-10-251104
- an object of the present invention is to provide an insecticidal and ovicidal composition having an ovicidal property that is not only pesticidal to agricultural crop pests.
- Another object of the present invention is to provide a method for killing insects and eggs of crop pests.
- the present invention provides the following insecticidal and ovicidal composition and method.
- An insecticidal and ovicidal composition comprising, as an active ingredient, at least one selected from the group consisting of coconut oil and palm kernel oil.
- An insecticidal and ovicidal composition comprising, as an active ingredient, at least one selected from the group consisting of tridalicelide containing a species as a constituent fatty acid.
- Tridaliceride containing saturated fatty acids having 12 carbon atoms and saturated fatty acids having 14 carbon atoms as constituent fatty acids (preferable mixture molar ratio is 14:14), saturated fatty acid having 12 carbon atoms and carbon atom
- Tridaliceride containing the unsaturated fatty acid of number 18 as a constituent fatty acid (preferable mixture molar ratio is 1-4: 14), saturated fatty acid of 12 carbon atoms, saturated fatty acid of 14 carbon atoms, and fatty acid of 18 carbon atoms.
- Tridaliceride containing unsaturated fatty acids as constituent fatty acids (preferable mixture molar ratio is 14:14 to 14:14), containing saturated fatty acids having 10 carbon atoms and unsaturated fatty acids having 18 carbon atoms as constituent fatty acids
- An insecticidal and ovicidal composition comprising, as an active ingredient, at least one selected from the group consisting of tridalicelide (preferable mixture molar ratio is 14:14), glycerin triolate, and glycerin trilaurate.
- 20% by mass or more of the constituent fatty acids are selected from the group consisting of saturated fatty acids having 10 carbon atoms, saturated fatty acids having 12 carbon atoms, saturated fatty acids having 14 carbon atoms, and unsaturated fatty acids having 18 carbon atoms.
- An insecticidal and ovicidal composition containing a fat or oil as an active ingredient.
- An insecticidal and ovicidal composition comprising, as an active ingredient, a fat or oil in which 20% by mass or more of the constituent fatty acids is lauric acid.
- An insecticidal and ovicidal composition comprising, as an active ingredient, a fat or oil in which at least 20% by mass of the constituent fatty acids is myristic acid.
- An insecticidal and ovicidal composition containing, as an active ingredient, a fat or oil in which 20% by mass or more of constituent fatty acids is oleic acid.
- the insecticidal and ovicidal composition according to item 1 is a group consisting of diglycerol oleate, diglycerin laurate, propylene glycol monolate, propylene glycol monorenolate and propylene glycol monorenoate.
- At least one interface selected from the group consisting of polyglycerin polyricinoleate, polyoxyethylene styrylphenyl ether ether, polyoxyethylene fatty acid ester, polyoxyethylene castor oil, and dodecinolebenzenesulfonate 11.
- the insecticidal and ovicidal composition according to any one of items 110 to 110, further comprising an activator.
- An insecticidal and ovicidal method which comprises spraying the insecticidal and ovicidal composition according to any one of (1) to (1) above in a range of 0.2 kg / 10a to 8 kg / 10a.
- the present invention has been completed based on the discovery that fats and oils having a specific fatty acid composition have an excellent insecticidal and ovicidal action on eggs of agricultural pests.
- the active ingredients of the insecticidal and ovicidal composition of the present invention include coconut oil, palm kernel oil, tridaliceride of a saturated fatty acid having 10, 12 or 14 carbon atoms, triglyceride of an unsaturated fatty acid having 18 carbon atoms, and carbon atom.
- Tridaliceride which contains at least two kinds of saturated fatty acids of the number 10, 12, or 14 and unsaturated fatty acids having 18 carbon atoms as constituent fatty acids is exemplified.
- a specific example of a saturated fatty acid having 10 carbon atoms is chlorophyllic acid
- a specific example of a saturated fatty acid having 12 carbon atoms is lauric acid
- a specific example of a saturated fatty acid having 14 carbon atoms is myristic acid.
- Specific examples of the unsaturated fatty acid having 18 carbon atoms include oleic acid.
- a tridaliceride of a saturated fatty acid having 12 carbon atoms glycerin trilaurate is mentioned.
- a tridaliceride of an unsaturated fatty acid having 18 carbon atoms glycerin trioleate is composed of 10 or 12 carbon atoms.
- 14 saturated fatty acids and 18 unsaturated carbon fatty acids examples include saturated fatty acids having 12 carbon atoms and saturated fatty acids having 14 carbon atoms as constituent fatty acids, saturated fatty acids having 12 carbon atoms and saturated fatty acids having 12 carbon atoms and 18 carbon atoms.
- Examples include triglycerides containing unsaturated fatty acids having 18 carbon atoms as constituent fatty acids and mixtures of two or more thereof.
- the content of the active ingredient is preferably 0.01 20 Weight 0/0, more preferably 0.1 5 wt 0/0.
- the insecticidal and ovicidal composition of the present invention may contain only the above-mentioned fats and oils. Or a mixture thereof), propylene glycol monolaurate, propylene glycol monopalmitate and propylene glycol monoolate.
- the content of these auxiliaries is preferably 5 to 70 parts by mass, more preferably 20 to 50 parts by mass, based on 100 parts by mass of the fat and oil of the active ingredient.
- the insecticidal and ovicidal composition of the present invention further comprises at least one selected from the group consisting of polyglycerin polyricinoleate, polyoxyethylene styrene phenyl ether, polyoxyethylene fatty acid ester, polyoxyethylene castor oil and dodecylbenzene sulfonate. It is preferred to contain a type of surfactant.
- the content of these surfactants is preferably 5-70 parts by mass, more preferably 520 parts by mass, per 100 parts by mass of the fat or oil as the active ingredient.
- the insecticidal and ovicidal composition of the present invention preferably contains an oil or fat as an active ingredient and the above-mentioned auxiliary agent, and more preferably contains the above-mentioned surfactant.
- the insecticidal and ovicidal composition of the present invention is preferably applied to crops in the range of 0.2 kg / 10a to 8 kg / 10a, more preferably 0.5 kg / 10a to 3 kg / 10a.
- the amount of oil and fat of the active ingredient is preferably 0. It is preferable to dilute with water or the like so that the concentration becomes about 05 to 5% by mass, more preferably about 0.2 to 0.5% by mass, and spray.
- the time of application depends on the type of pest, but usually it can be applied from the beginning to the end of spawning. Spraying at an earlier time is effective, but the composition of the present invention is effective even if sprayed after confirming oviposition due to its high ovicidal properties.
- the insecticidal and ovicidal composition of the present invention is effective for insecticidal and ovicidal insect pests of all kinds of crops.
- Examples of the target pests include the following.
- Lepidoptera Mulch (Mamestra brassicae), Apod (Leucania separata), Plutella (Plutella macuiipennis)
- Dermatophagoids Citrus mite (Aculus pelekassi), Tomato rust mite (Aculops lycopersici) Dust mites: Cyanodicori (Brevipalpus obovatus)
- Aphids Aphis gossypii, Peach aphid (Myzus persicae), Potato beetle aphid (Aulacorthum solani)
- Hemiptera Whitefly (Trialeurodes vaporariorus), Tobacco whitefly (Bemisia tabaci)
- Pests that exhibit particularly pronounced ovicidal effects are Lepidoptera, Chrysomelidae, Pterodactyls, Dermatophagoides, Acarids, and Aphids.
- a test solution diluted to a predetermined concentration was sprayed on eggplant seedlings damaged by Chianohokoridida2. After that, they were kept in a glass greenhouse and the degree of damage to newly emerging shoots was examined. 4.Effect on whitefly
- a test solution diluted to a predetermined concentration was sprayed on the leaves of the cucumber, which inhabited the 3-4th larvae. Thereafter, the cells were kept in a glass greenhouse, and after 4 days, the survival and death of whitefly larvae were determined under a microscope and counted.
- a reagent solution diluted to a predetermined concentration was sprayed on a petal beetle that inhabits the back side of the true leaves of Cucumber. After that, they were kept in a glass greenhouse, and after 4 days, the viability of P. aphid was determined and counted.
- a reagent solution diluted to a predetermined concentration was sprayed on the wood scale insects living on the citrus leaves. After that, the cells were kept in a glass greenhouse, and after 4 days, the life and death of the larvae of the scale insects were determined under a microscope and counted.
- a ladybug egg laid on a medicine wrapper was used for the experiment.
- the egg mass was cut into 415 pieces, one of which was left untreated, and the other was used for the effect test.
- the egg mass was immersed for about 30 seconds in a reagent solution diluted to a predetermined concentration together with a packaging paper. After water was sufficiently removed from the filter paper, the cells were placed in a petri dish and cultured at 25 ° C, and the number of larvae was counted after 7 days.
- paraffin paper Artemisia eggs laid on paraffin paper were used in the experiments.
- the paraffin paper was cut into about 100 120 eggs and immersed in a reagent solution diluted to a predetermined concentration for about 30 seconds. After removing excess water with a filter paper and drying sufficiently, the cells were cultured in a petri dish. Larvae were counted 10 days later.
- the damage was classified into the following degrees and investigated.
- nl, ⁇ 2, ⁇ 3, ⁇ 4 are the respective numbers, and ⁇ is the total number.
- Control effect (%) Degree of damage in untreated areas ⁇ Degree of damage in treated areas
- Insecticulation rate (%) 100 * number of dead larvae / total number of larvae
- Insecticulation rate (%) 100 * number of dead larvae / total number of larvae
- Hatching rate (%) Number of eggs hatched / Total number of eggs
- Hatching rate (%) loo X Number of taint marks in treated area Z Number of taint marks in untreated area
- Hatching rate (%) loo X Number of eggs hatched Z Total number of eggs
- Larvicidal rate (%) loo X number of larvae in the treated area Z number of larvae in the untreated area
- Solpol CA-42 Polyoxyethylene (40) castor oil
- Solpol 355H (mixture of Solpol T-20, Solpol ⁇ -26, Solpol EX-15 and alkynolebenzene)
- Solpol ⁇ -20 Polyoxyethylene styryl phenyl ether (HLB13.3)
- Solpol ⁇ -26 Polyoxyethylene styryl phenyl ether (HLB 14.4)
- Solpol EX-15 Calcium alkylarylsulfonate
- Riquemanore # 205 polyoxyethylene lauryl ether
- Liquemar L-71-D Diglycerin laurate (single or mixture from monolaurate to hexalaperate)
- Lichemanore 0-71-D Diglycerol oleate (single or mixture from monoolate to hexolate)
- Actor M-1 Tricaprylin (70 mass 0/0) / tri force purine (30 mass 0/0)
- Actor M-2 Tricaprylin
- ⁇ GNOL 14-0 Polyoxyethylene oleyl ester
- Phosphanol ML-200 Laurinoleic acid
- Auxiliary agent A Solpol 355H + Liquemar DO-100 + Soybean oil
- Auxiliary B Riquemar B205 + Riquemar 0-71-D + M- 2
- Auxiliary agent C Solpol 355H + soybean oil + AG-7520
- Auxiliary agent E Riquemar DO-100 + soybean oil
- Auxiliary agent F Riquemar DO-100 + olive oil
- Solpol is a trade name of Toho Chemical Industry Co., Ltd., and Riquemar and Actor are trade names of Riken Vitamin.
- a formulation in which coconut oil and auxiliary agent A (actor M-1 + Solpol 355H + liquemar DO-100 are mixed in a ratio of 1: 1: 1) are mixed in a ratio of 8: 2.
- a formulation in which coconut oil and auxiliaries B (actor M-2 + liquemar B205 + liquemar 0-71-D are mixed in a ratio of 1: 1: 1) are mixed in a ratio of 8: 2.
- palm kernel oil and auxiliary agent C a mixture of soybean oil + Solpol 355H + AG-7520 in a ratio of 1: 1: 1 are mixed in a ratio of 8: 2.
- rapeseed oil and auxiliary agent A a mixture of soybean oil + Solpol 355H + liquemar DO-100 at a ratio of 1: 1: 1) are mixed at a ratio of 8: 2.
- Comparative Example 4 A formulation comprising a mixture of castor oil and D composition (actor M-1 + liquemar B205 + liquemar 0-71-D (manufactured by RIKEN Vitamin) in a ratio of 1: 1: 1) in a ratio of 8: 2.
- Olive oil and auxiliaries C (a mixture of soybean oil + Solpol 355H + AG-7520 in a ratio of 1: 1: 1) in a ratio of 8: 2.
- the drug concentration is 300mg / 100ml.
- the conventional insecticidal composition is intended for controlling adult and larvae of agricultural pests, and does not reduce or inhibit the hatching ability of the insect pests, whereas the insecticidal oocyte-killing composition of the present invention Has the ability to kill eggs and larvae of agricultural crop pests because it has oviposition properties in addition to insecticidal properties, and can reduce or inhibit the hatching ability of eggs already laid in crops and soil. In addition, it is possible to effectively prevent or reduce crop damage caused by pests.
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- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Zoology (AREA)
- Agronomy & Crop Science (AREA)
- Plant Pathology (AREA)
- Dentistry (AREA)
- Wood Science & Technology (AREA)
- Environmental Sciences (AREA)
- Pest Control & Pesticides (AREA)
- Biotechnology (AREA)
- Microbiology (AREA)
- Mycology (AREA)
- Natural Medicines & Medicinal Plants (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Priority Applications (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP04747270A EP1645187A1 (en) | 2003-07-10 | 2004-07-09 | Insecticidal ovicidal composition |
| US11/327,423 US20060165748A1 (en) | 2003-07-10 | 2006-01-09 | Insecticidal and ovicidal composition |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2003194837A JP2005029489A (ja) | 2003-07-10 | 2003-07-10 | 殺虫殺卵組成物 |
| JP2003-194837 | 2003-07-10 |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US11/327,423 Continuation US20060165748A1 (en) | 2003-07-10 | 2006-01-09 | Insecticidal and ovicidal composition |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| WO2005004602A1 true WO2005004602A1 (ja) | 2005-01-20 |
Family
ID=34055702
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/JP2004/009802 Ceased WO2005004602A1 (ja) | 2003-07-10 | 2004-07-09 | 殺虫殺卵組成物 |
Country Status (4)
| Country | Link |
|---|---|
| US (1) | US20060165748A1 (https=) |
| EP (1) | EP1645187A1 (https=) |
| JP (1) | JP2005029489A (https=) |
| WO (1) | WO2005004602A1 (https=) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20150230459A1 (en) * | 2006-04-07 | 2015-08-20 | Riken | Pesticidal/ovicidal composition and pesticidal/ovicidal method |
| JPWO2022158590A1 (https=) * | 2021-01-25 | 2022-07-28 |
Families Citing this family (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP2005825A4 (en) * | 2006-04-07 | 2012-03-28 | Riken | INSECTICIDE OVICIDAL COMPOSITION AND METHODS OF INSECT AND EYE PROTECTION |
| KR100758371B1 (ko) | 2006-08-10 | 2007-09-14 | 한국생명공학연구원 | 살충제 |
| WO2010115002A2 (en) * | 2009-04-03 | 2010-10-07 | Croda, Inc. | Pest control composition |
| EP2543251B1 (en) * | 2010-03-01 | 2015-05-13 | Nippon Kayaku Kabushiki Kaisha | Pest controlling composition |
| MX355432B (es) | 2010-09-14 | 2018-04-18 | Basf Se | Composiciones que contienen un insecticida de piripiropeno y una base. |
| JP6425887B2 (ja) | 2010-09-14 | 2018-11-21 | ビーエーエスエフ ソシエタス・ヨーロピアBasf Se | ピリピロペン殺虫剤及び補助剤を含有する組成物 |
| JP2012246251A (ja) * | 2011-05-27 | 2012-12-13 | Sumitomo Chemical Garden Products Inc | 農園芸用殺虫組成物 |
| JP6034027B2 (ja) * | 2012-02-21 | 2016-11-30 | アース製薬株式会社 | 有害生物防除剤及び有害生物防除方法 |
| EP2825043B1 (en) | 2012-03-12 | 2018-09-05 | Basf Se | Method for producing an aqueous suspension concentrate formulation of a pyripyropene insecticide |
| ES2566911T3 (es) | 2012-03-12 | 2016-04-18 | Basf Se | Formulación de concentrado líquido que contiene un insecticida de piripiropeno I |
| ES2566910T3 (es) | 2012-03-12 | 2016-04-18 | Basf Se | Formulación de concentrado líquido que contiene un insecticida de piripiropeno II |
| BR112014022648B1 (pt) * | 2012-03-13 | 2021-05-25 | Basf Se | formulação de concentrado líquido, preparação aquosa, métodos para proteger plantas, não-terapêutico para controlar pragas invertebradas e para proteção de material de propagação de planta contra pragas invertebradas, e usos de uma formulação |
| ES2698505T3 (es) * | 2012-03-23 | 2019-02-05 | Dow Agrosciences Llc | Concentrados acuosos de herbicidas que contienen ésteres alquílicos de ácidos grasos, amidas de ácidos grasos o ésteres de ácidos grasos triglicéridos y métodos de uso |
| CN107849337B (zh) * | 2015-08-27 | 2021-02-23 | 日本瑞翁株式会社 | 树脂组合物及树脂成型体 |
| IT202000004816A1 (it) * | 2020-03-06 | 2021-09-06 | Alpha Biopesticides Ltd | Composizione pesticida per la cura e la protezione delle coltivazioni |
| US12342828B2 (en) | 2020-09-14 | 2025-07-01 | Insight Pharmaceuticals Corporation | Repellant formulation and method |
| CN113475503B (zh) * | 2021-07-28 | 2022-12-02 | 广东省科学院动物研究所 | 一种农药用三油酸甘油酯乳剂及其应用 |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH10251104A (ja) * | 1997-03-07 | 1998-09-22 | Rikagaku Kenkyusho | 殺虫殺ダニ組成物及び殺虫殺ダニ方法 |
| JPH1129411A (ja) * | 1997-07-10 | 1999-02-02 | Sankei Kagaku Kk | 農園芸用殺虫殺菌剤組成物 |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA2130375C (en) * | 1993-10-01 | 2004-08-17 | Lynn Sue James | Insecticide and insect repellant compositions |
| US5496857A (en) * | 1994-03-17 | 1996-03-05 | Targosz; Eugene F. | Whitefly insecticide |
| US6176842B1 (en) * | 1995-03-08 | 2001-01-23 | Ekos Corporation | Ultrasound assembly for use with light activated drugs |
-
2003
- 2003-07-10 JP JP2003194837A patent/JP2005029489A/ja active Pending
-
2004
- 2004-07-09 WO PCT/JP2004/009802 patent/WO2005004602A1/ja not_active Ceased
- 2004-07-09 EP EP04747270A patent/EP1645187A1/en not_active Withdrawn
-
2006
- 2006-01-09 US US11/327,423 patent/US20060165748A1/en not_active Abandoned
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH10251104A (ja) * | 1997-03-07 | 1998-09-22 | Rikagaku Kenkyusho | 殺虫殺ダニ組成物及び殺虫殺ダニ方法 |
| JPH1129411A (ja) * | 1997-07-10 | 1999-02-02 | Sankei Kagaku Kk | 農園芸用殺虫殺菌剤組成物 |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20150230459A1 (en) * | 2006-04-07 | 2015-08-20 | Riken | Pesticidal/ovicidal composition and pesticidal/ovicidal method |
| US10130094B2 (en) | 2006-04-07 | 2018-11-20 | Riken | Pesticidal/ovicidal composition and pesticidal/ovicidal method |
| JPWO2022158590A1 (https=) * | 2021-01-25 | 2022-07-28 | ||
| WO2022158590A1 (ja) * | 2021-01-25 | 2022-07-28 | 国立研究開発法人理化学研究所 | ハダニ忌避剤 |
| JP7755864B2 (ja) | 2021-01-25 | 2025-10-17 | 国立研究開発法人理化学研究所 | ハダニ忌避剤 |
Also Published As
| Publication number | Publication date |
|---|---|
| JP2005029489A (ja) | 2005-02-03 |
| EP1645187A1 (en) | 2006-04-12 |
| US20060165748A1 (en) | 2006-07-27 |
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