IL28633A - Insecticidal and fungicidal compositions containing benzylidene-malonic acid derivatives - Google Patents

Insecticidal and fungicidal compositions containing benzylidene-malonic acid derivatives

Info

Publication number: IL28633A
Authority: IL; Israel
Prior art keywords: general formula; compound represented; composition containing; active ingredient; fungicidal
Prior art date: 1966-09-22

Application number

IL28633A

Other languages

English (en)

Original Assignee

Sumitomo Chemical Co

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1966-09-22

Filing date

1967-09-12

Publication date

1972-06-28

1967-09-12 Application filed by Sumitomo Chemical Co filed Critical Sumitomo Chemical Co

1972-06-28 Publication of IL28633A publication Critical patent/IL28633A/en

Links

239000000203 mixture Substances 0.000 title claims description 31
230000000855 fungicidal effect Effects 0.000 title claims description 20
230000000749 insecticidal effect Effects 0.000 title claims description 14
KXTAOXNYQGASTA-UHFFFAOYSA-N 2-benzylidenepropanedioic acid Chemical class OC(=O)C(C(O)=O)=CC1=CC=CC=C1 KXTAOXNYQGASTA-UHFFFAOYSA-N 0.000 title 1
150000001875 compounds Chemical class 0.000 claims description 70
239000004480 active ingredient Substances 0.000 claims description 18
239000002075 main ingredient Substances 0.000 claims description 5
125000000217 alkyl group Chemical group 0.000 claims description 4
125000004093 cyano group Chemical group *C#N 0.000 claims description 4
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 4
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 2
241000209094 Oryza Species 0.000 description 28
239000000428 dust Substances 0.000 description 26
239000000417 fungicide Substances 0.000 description 18
235000007164 Oryza sativa Nutrition 0.000 description 17
235000009566 rice Nutrition 0.000 description 17
239000000126 substance Substances 0.000 description 17
230000000694 effects Effects 0.000 description 11
241000238631 Hexapoda Species 0.000 description 10
239000002917 insecticide Substances 0.000 description 10
230000003449 preventive effect Effects 0.000 description 10
ZNOLGFHPUIJIMJ-UHFFFAOYSA-N fenitrothion Chemical compound COP(=S)(OC)OC1=CC=C([N+]([O-])=O)C(C)=C1 ZNOLGFHPUIJIMJ-UHFFFAOYSA-N 0.000 description 9
239000004563 wettable powder Substances 0.000 description 8
230000000266 injurious effect Effects 0.000 description 7
125000000962 organic group Chemical group 0.000 description 7
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 6
238000002360 preparation method Methods 0.000 description 6
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
239000000454 talc Substances 0.000 description 5
229910052623 talc Inorganic materials 0.000 description 5
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
239000005947 Dimethoate Substances 0.000 description 4
239000004927 clay Substances 0.000 description 4
230000001627 detrimental effect Effects 0.000 description 4
MCWXGJITAZMZEV-UHFFFAOYSA-N dimethoate Chemical compound CNC(=O)CSP(=S)(OC)OC MCWXGJITAZMZEV-UHFFFAOYSA-N 0.000 description 4
238000010410 dusting Methods 0.000 description 4
238000009472 formulation Methods 0.000 description 4
UPHVDBIPEJJINY-UHFFFAOYSA-L iron(2+);methyl-dioxido-oxo-$l^{5}-arsane Chemical compound [Fe+2].C[As]([O-])([O-])=O UPHVDBIPEJJINY-UHFFFAOYSA-L 0.000 description 4
239000007788 liquid Substances 0.000 description 4
238000002156 mixing Methods 0.000 description 4
239000000843 powder Substances 0.000 description 4
230000002265 prevention Effects 0.000 description 4
241000238876 Acari Species 0.000 description 3
241000283690 Bos taurus Species 0.000 description 3
241000196324 Embryophyta Species 0.000 description 3
239000004495 emulsifiable concentrate Substances 0.000 description 3
229940100892 mercury compound Drugs 0.000 description 3
238000009736 wetting Methods 0.000 description 3
MEKOFIRRDATTAG-UHFFFAOYSA-N 2,2,5,8-tetramethyl-3,4-dihydrochromen-6-ol Chemical compound C1CC(C)(C)OC2=C1C(C)=C(O)C=C2C MEKOFIRRDATTAG-UHFFFAOYSA-N 0.000 description 2
DOZRDZLFLOODMB-UHFFFAOYSA-N 3,5-di-tert-Butyl-4-hydroxybenzaldehyde Chemical compound CC(C)(C)C1=CC(C=O)=CC(C(C)(C)C)=C1O DOZRDZLFLOODMB-UHFFFAOYSA-N 0.000 description 2
239000005995 Aluminium silicate Substances 0.000 description 2
241001414720 Cicadellidae Species 0.000 description 2
241000254173 Coleoptera Species 0.000 description 2
241000255925 Diptera Species 0.000 description 2
AIGRXSNSLVJMEA-UHFFFAOYSA-N EPN Chemical compound C=1C=CC=CC=1P(=S)(OCC)OC1=CC=C([N+]([O-])=O)C=C1 AIGRXSNSLVJMEA-UHFFFAOYSA-N 0.000 description 2
241000358422 Nephotettix cincticeps Species 0.000 description 2
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
241001454293 Tetranychus urticae Species 0.000 description 2
239000000654 additive Substances 0.000 description 2
239000003905 agrochemical Substances 0.000 description 2
235000012211 aluminium silicate Nutrition 0.000 description 2
230000003115 biocidal effect Effects 0.000 description 2
239000012141 concentrate Substances 0.000 description 2
239000000470 constituent Substances 0.000 description 2
JXSJBGJIGXNWCI-UHFFFAOYSA-N diethyl 2-[(dimethoxyphosphorothioyl)thio]succinate Chemical compound CCOC(=O)CC(SP(=S)(OC)OC)C(=O)OCC JXSJBGJIGXNWCI-UHFFFAOYSA-N 0.000 description 2
201000010099 disease Diseases 0.000 description 2
208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 2
239000003995 emulsifying agent Substances 0.000 description 2
239000004009 herbicide Substances 0.000 description 2
NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 2
PVTHJAPFENJVNC-MHRBZPPQSA-N kasugamycin Chemical compound N[C@H]1C[C@H](NC(=N)C(O)=O)[C@@H](C)O[C@@H]1O[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@H](O)[C@@H]1O PVTHJAPFENJVNC-MHRBZPPQSA-N 0.000 description 2
238000000034 method Methods 0.000 description 2
GTCAXTIRRLKXRU-UHFFFAOYSA-N methyl carbamate Chemical compound COC(N)=O GTCAXTIRRLKXRU-UHFFFAOYSA-N 0.000 description 2
UCSJYZPVAKXKNQ-HZYVHMACSA-N streptomycin Chemical compound CN[C@H]1[C@H](O)[C@@H](O)[C@H](CO)O[C@H]1O[C@@H]1[C@](C=O)(O)[C@H](C)O[C@H]1O[C@@H]1[C@@H](NC(N)=N)[C@H](O)[C@@H](NC(N)=N)[C@H](O)[C@H]1O UCSJYZPVAKXKNQ-HZYVHMACSA-N 0.000 description 2
230000004083 survival effect Effects 0.000 description 2
RYYWUUFWQRZTIU-UHFFFAOYSA-K thiophosphate Chemical compound [O-]P([O-])([O-])=S RYYWUUFWQRZTIU-UHFFFAOYSA-K 0.000 description 2
231100000419 toxicity Toxicity 0.000 description 2
230000001988 toxicity Effects 0.000 description 2
ZCVAOQKBXKSDMS-AQYZNVCMSA-N (+)-trans-allethrin Chemical compound CC1(C)[C@H](C=C(C)C)[C@H]1C(=O)OC1C(C)=C(CC=C)C(=O)C1 ZCVAOQKBXKSDMS-AQYZNVCMSA-N 0.000 description 1
OHVLMTFVQDZYHP-UHFFFAOYSA-N 1-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)-2-[4-[2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidin-5-yl]piperazin-1-yl]ethanone Chemical group N1N=NC=2CN(CCC=21)C(CN1CCN(CC1)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F)=O OHVLMTFVQDZYHP-UHFFFAOYSA-N 0.000 description 1
KZEVSDGEBAJOTK-UHFFFAOYSA-N 1-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)-2-[5-[2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidin-5-yl]-1,3,4-oxadiazol-2-yl]ethanone Chemical group N1N=NC=2CN(CCC=21)C(CC=1OC(=NN=1)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F)=O KZEVSDGEBAJOTK-UHFFFAOYSA-N 0.000 description 1
FMTFEIJHMMQUJI-NJAFHUGGSA-N 102130-98-3 Natural products CC=CCC1=C(C)[C@H](CC1=O)OC(=O)[C@@H]1[C@@H](C=C(C)C)C1(C)C FMTFEIJHMMQUJI-NJAFHUGGSA-N 0.000 description 1
ORIHZIZPTZTNCU-UHFFFAOYSA-N 2-(hydroxyiminomethyl)phenol Chemical compound ON=CC1=CC=CC=C1O ORIHZIZPTZTNCU-UHFFFAOYSA-N 0.000 description 1
NPHULPIAPWNOOH-UHFFFAOYSA-N 2-[4-[2-(2,3-dihydro-1H-inden-2-ylamino)pyrimidin-5-yl]-3-(2,3-dihydroindol-1-ylmethyl)pyrazol-1-yl]-1-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)ethanone Chemical group C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)C=1C(=NN(C=1)CC(=O)N1CC2=C(CC1)NN=N2)CN1CCC2=CC=CC=C12 NPHULPIAPWNOOH-UHFFFAOYSA-N 0.000 description 1
JQMFQLVAJGZSQS-UHFFFAOYSA-N 2-[4-[2-(2,3-dihydro-1H-inden-2-ylamino)pyrimidin-5-yl]piperazin-1-yl]-N-(2-oxo-3H-1,3-benzoxazol-6-yl)acetamide Chemical group C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)N1CCN(CC1)CC(=O)NC1=CC2=C(NC(O2)=O)C=C1 JQMFQLVAJGZSQS-UHFFFAOYSA-N 0.000 description 1
JVKRKMWZYMKVTQ-UHFFFAOYSA-N 2-[4-[2-(2,3-dihydro-1H-inden-2-ylamino)pyrimidin-5-yl]pyrazol-1-yl]-N-(2-oxo-3H-1,3-benzoxazol-6-yl)acetamide Chemical group C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)C=1C=NN(C=1)CC(=O)NC1=CC2=C(NC(O2)=O)C=C1 JVKRKMWZYMKVTQ-UHFFFAOYSA-N 0.000 description 1
CYJRNFFLTBEQSQ-UHFFFAOYSA-N 8-(3-methyl-1-benzothiophen-5-yl)-N-(4-methylsulfonylpyridin-3-yl)quinoxalin-6-amine Chemical compound CS(=O)(=O)C1=C(C=NC=C1)NC=1C=C2N=CC=NC2=C(C=1)C=1C=CC2=C(C(=CS2)C)C=1 CYJRNFFLTBEQSQ-UHFFFAOYSA-N 0.000 description 1
QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
241000223600 Alternaria Species 0.000 description 1
KXDHJXZQYSOELW-UHFFFAOYSA-M Carbamate Chemical group NC([O-])=O KXDHJXZQYSOELW-UHFFFAOYSA-M 0.000 description 1
241000426497 Chilo suppressalis Species 0.000 description 1
239000005749 Copper compound Substances 0.000 description 1
241000256059 Culex pipiens Species 0.000 description 1
241000256113 Culicidae Species 0.000 description 1
239000004606 Fillers/Extenders Substances 0.000 description 1
241000233866 Fungi Species 0.000 description 1
241000258937 Hemiptera Species 0.000 description 1
239000005909 Kieselgur Substances 0.000 description 1
NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 1
UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 1
241000244206 Nematoda Species 0.000 description 1
244000046052 Phaseolus vulgaris Species 0.000 description 1
231100000674 Phytotoxicity Toxicity 0.000 description 1
229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
VQXSOUPNOZTNAI-UHFFFAOYSA-N Pyrethrin I Natural products CC(=CC1CC1C(=O)OC2CC(=O)C(=C2C)CC=C/C=C)C VQXSOUPNOZTNAI-UHFFFAOYSA-N 0.000 description 1
241001454294 Tetranychus Species 0.000 description 1
239000000642 acaricide Substances 0.000 description 1
239000002253 acid Substances 0.000 description 1
230000000996 additive effect Effects 0.000 description 1
229940024113 allethrin Drugs 0.000 description 1
239000003242 anti bacterial agent Substances 0.000 description 1
229940088710 antibiotic agent Drugs 0.000 description 1
239000000969 carrier Substances 0.000 description 1
JBTGHKUTYAMZEZ-UHFFFAOYSA-N cellocidin Chemical compound NC(=O)C#CC(N)=O JBTGHKUTYAMZEZ-UHFFFAOYSA-N 0.000 description 1
235000013339 cereals Nutrition 0.000 description 1
238000006243 chemical reaction Methods 0.000 description 1
229960005091 chloramphenicol Drugs 0.000 description 1
WIIZWVCIJKGZOK-RKDXNWHRSA-N chloramphenicol Chemical compound ClC(Cl)C(=O)N[C@H](CO)[C@H](O)C1=CC=C([N+]([O-])=O)C=C1 WIIZWVCIJKGZOK-RKDXNWHRSA-N 0.000 description 1
238000009833 condensation Methods 0.000 description 1
230000005494 condensation Effects 0.000 description 1
150000001880 copper compounds Chemical class 0.000 description 1
230000018044 dehydration Effects 0.000 description 1
238000006297 dehydration reaction Methods 0.000 description 1
XFMJUIKWKVJNDY-UHFFFAOYSA-N diethoxyphosphorylsulfanylmethylbenzene Chemical compound CCOP(=O)(OCC)SCC1=CC=CC=C1 XFMJUIKWKVJNDY-UHFFFAOYSA-N 0.000 description 1
HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 1
YDEXUEFDPVHGHE-GGMCWBHBSA-L disodium;(2r)-3-(2-hydroxy-3-methoxyphenyl)-2-[2-methoxy-4-(3-sulfonatopropyl)phenoxy]propane-1-sulfonate Chemical compound [Na+].[Na+].COC1=CC=CC(C[C@H](CS([O-])(=O)=O)OC=2C(=CC(CCCS([O-])(=O)=O)=CC=2)OC)=C1O YDEXUEFDPVHGHE-GGMCWBHBSA-L 0.000 description 1
235000013399 edible fruits Nutrition 0.000 description 1
239000003337 fertilizer Substances 0.000 description 1
244000053095 fungal pathogen Species 0.000 description 1
229940093920 gynecological arsenic compound Drugs 0.000 description 1
238000010348 incorporation Methods 0.000 description 1
239000004615 ingredient Substances 0.000 description 1
XEEYBQQBJWHFJM-UHFFFAOYSA-N iron Substances [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 1
229910052742 iron Inorganic materials 0.000 description 1
238000004898 kneading Methods 0.000 description 1
229910052753 mercury Inorganic materials 0.000 description 1
229940043265 methyl isobutyl ketone Drugs 0.000 description 1
UFEJKYYYVXYMMS-UHFFFAOYSA-N methylcarbamic acid Chemical compound CNC(O)=O UFEJKYYYVXYMMS-UHFFFAOYSA-N 0.000 description 1
239000011812 mixed powder Substances 0.000 description 1
230000001069 nematicidal effect Effects 0.000 description 1
239000005645 nematicide Substances 0.000 description 1
150000002898 organic sulfur compounds Chemical class 0.000 description 1
239000003986 organophosphate insecticide Substances 0.000 description 1
LCCNCVORNKJIRZ-UHFFFAOYSA-N parathion Chemical compound CCOP(=S)(OCC)OC1=CC=C([N+]([O-])=O)C=C1 LCCNCVORNKJIRZ-UHFFFAOYSA-N 0.000 description 1
239000000546 pharmaceutical excipient Substances 0.000 description 1
150000002989 phenols Chemical class 0.000 description 1
229910052698 phosphorus Inorganic materials 0.000 description 1
239000011574 phosphorus Substances 0.000 description 1
-1 polyoxyethylene Polymers 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
VJFUPGQZSXIULQ-XIGJTORUSA-N pyrethrin II Chemical compound CC1(C)[C@H](/C=C(\C)C(=O)OC)[C@H]1C(=O)O[C@@H]1C(C)=C(C\C=C/C=C)C(=O)C1 VJFUPGQZSXIULQ-XIGJTORUSA-N 0.000 description 1
239000007921 spray Substances 0.000 description 1
238000003756 stirring Methods 0.000 description 1
229960005322 streptomycin Drugs 0.000 description 1
230000002195 synergetic effect Effects 0.000 description 1
CXBMCYHAMVGWJQ-UHFFFAOYSA-N tetramethrin Chemical compound CC1(C)C(C=C(C)C)C1C(=O)OCN1C(=O)C(CCCC2)=C2C1=O CXBMCYHAMVGWJQ-UHFFFAOYSA-N 0.000 description 1
231100000331 toxic Toxicity 0.000 description 1
230000002588 toxic effect Effects 0.000 description 1
231100000701 toxic element Toxicity 0.000 description 1
238000009834 vaporization Methods 0.000 description 1
230000008016 vaporization Effects 0.000 description 1
235000013311 vegetables Nutrition 0.000 description 1
JLYXXMFPNIAWKQ-UHFFFAOYSA-N γ Benzene hexachloride Chemical compound ClC1C(Cl)C(Cl)C(Cl)C(Cl)C1Cl JLYXXMFPNIAWKQ-UHFFFAOYSA-N 0.000 description 1

Classifications

- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
- A01N25/02—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests containing liquids as carriers, diluents or solvents
- A01N25/04—Dispersions, emulsions, suspoemulsions, suspension concentrates or gels
- 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
- A01N2300/00—Combinations or mixtures of active ingredients covered by classes A01N27/00 - A01N65/48 with other active or formulation relevant ingredients, e.g. specific carrier materials or surfactants, covered by classes A01N25/00 - A01N65/48

Landscapes

Life Sciences & Earth Sciences (AREA)
General Health & Medical Sciences (AREA)
Health & Medical Sciences (AREA)
Toxicology (AREA)
Agronomy & Crop Science (AREA)
Dispersion Chemistry (AREA)
Pest Control & Pesticides (AREA)
Plant Pathology (AREA)
Chemical & Material Sciences (AREA)
Engineering & Computer Science (AREA)
Dentistry (AREA)
Wood Science & Technology (AREA)
Zoology (AREA)
Environmental Sciences (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

IL28633A 1966-09-22 1967-09-12 Insecticidal and fungicidal compositions containing benzylidene-malonic acid derivatives IL28633A (en)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
JP6277066		1966-09-22
JP7062066		1966-10-25

Publications (1)

Publication Number	Publication Date
IL28633A true IL28633A (en)	1972-06-28

Family

ID=26403823

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
IL28633A IL28633A (en)	1966-09-22	1967-09-12	Insecticidal and fungicidal compositions containing benzylidene-malonic acid derivatives

Country Status (7)

Country	Link
BE (1)	BE704161A (de)
CH (1)	CH490015A (de)
DK (1)	DK115156B (de)
ES (1)	ES345227A1 (de)
GB (1)	GB1185509A (de)
IL (1)	IL28633A (de)
NL (1)	NL138850B (de)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US8414870B2 (en) *	2010-12-06	2013-04-09	Sytheon, Ltd.	Benzylidene substituted 2,4-pentanedione compounds and use thereof as stabilizers

1967
- 1967-09-12 IL IL28633A patent/IL28633A/en unknown
- 1967-09-15 NL NL676712638A patent/NL138850B/xx not_active IP Right Cessation
- 1967-09-20 ES ES345227A patent/ES345227A1/es not_active Expired
- 1967-09-20 GB GB42855/67A patent/GB1185509A/en not_active Expired
- 1967-09-21 BE BE704161D patent/BE704161A/xx unknown
- 1967-09-21 DK DK472467AA patent/DK115156B/da unknown
- 1967-09-22 CH CH1326067A patent/CH490015A/de not_active IP Right Cessation

Also Published As

Publication number	Publication date
BE704161A (de)	1968-02-01
DK115156B (da)	1969-09-08
CH490015A (de)	1970-05-15
GB1185509A (en)	1970-03-25
NL6712638A (de)	1968-03-25
DE1618955B2 (de)	1975-09-11
ES345227A1 (es)	1969-01-16
NL138850B (nl)	1973-05-15
DE1618955A1 (de)	1972-04-13

Publication	Publication Date	Title
US3899586A (en)	1975-08-12	Synergistic chrysanthemate insecticides
PL112140B1 (en)	1980-09-30	Insecticide
KR101290948B1 (ko)	2013-07-29	유해 생물 방제 조성물 및 유해 생물의 방제 방법
US4210642A (en)	1980-07-01	Insecticidal and acaricidal compositions
US2330234A (en)	1943-09-28	Insecticide
JPS6324483B2 (de)	1988-05-20
SU609453A3 (ru)	1978-05-30	Инсектицидно -акарицидна композици на основе сложного эфира циклопропанкарбоновой кислоты
US3105000A (en)	1963-09-24	Organo-tin and organo-sulphur parasiticides
US3535424A (en)	1970-10-20	Insecticidal 1 - (4 - hydroxy - 3,5 - di - tert butylphenyl) - 2-mono or disubstituted ethylenes
IL28633A (en)	1972-06-28	Insecticidal and fungicidal compositions containing benzylidene-malonic acid derivatives
US3995053A (en)	1976-11-30	Acaricidal and insecticidal compositions
US3538226A (en)	1970-11-03	Method of destroying plant fungi
HRP930934A2 (en)	1995-12-31	New method of combatting insect eggs and ovicidal compositions
US2590536A (en)	1952-03-25	Ground parts of ryania plant as insecticides
SU247148A1 (ru)		Инсектофунгицидный состав
JPS6037082B2 (ja)	1985-08-24	混合殺虫組成物
IL32202A (en)	1972-08-30	1-alkoxy-or-aryloxy-1-thiono-3-halogen-or-3-alkyl phospholines,their preparation and use for combatting pests
KR860000335B1 (ko)	1986-04-12	곤충 살충제 조성물
US4216213A (en)	1980-08-05	Acaricidal and insecticidal compositions
US4500521A (en)	1985-02-19	Pesticidal composition containing a synergistic combination of an oxazolo-pyridine thiophosphate derivative and cypermethrin
DE1618955C3 (de)	1976-04-29	Fungizide und insektizide Mittel
KR840001227B1 (ko)	1984-08-23	살충제 조성물
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