NO832456L - Insekticid-preparater - Google Patents

Insekticid-preparater

Info

Publication number: NO832456L
Authority: NO; Norway
Prior art keywords: phospholipid; mixture; dissolved; solvent; phosphatidylethanolamine
Prior art date: 1982-07-10

Application number

NO832456A

Other languages

English (en)

Norwegian (no)

Inventor

Miklos Ghyczy

Paul-Robert Imberge

Armin Wendal

Original Assignee

Nattermann A & Cie

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.)

1982-07-10

Filing date

1983-07-05

Publication date

1984-01-11

1983-07-05 Application filed by Nattermann A & Cie filed Critical Nattermann A & Cie

1984-01-11 Publication of NO832456L publication Critical patent/NO832456L/no

Links

150000003904 phospholipids Chemical class 0.000 claims description 28
239000000203 mixture Substances 0.000 claims description 21
238000002360 preparation method Methods 0.000 claims description 20
239000013543 active substance Substances 0.000 claims description 15
239000002904 solvent Substances 0.000 claims description 10
VEMKTZHHVJILDY-UXHICEINSA-N bioresmethrin Chemical compound CC1(C)[C@H](C=C(C)C)[C@H]1C(=O)OCC1=COC(CC=2C=CC=CC=2)=C1 VEMKTZHHVJILDY-UXHICEINSA-N 0.000 claims description 9
WTJKGGKOPKCXLL-RRHRGVEJSA-N phosphatidylcholine Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@H](COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCCCCCCC=CCCCCCCCC WTJKGGKOPKCXLL-RRHRGVEJSA-N 0.000 claims description 9
JZNWSCPGTDBMEW-UHFFFAOYSA-N Glycerophosphorylethanolamin Natural products NCCOP(O)(=O)OCC(O)CO JZNWSCPGTDBMEW-UHFFFAOYSA-N 0.000 claims description 8
238000010438 heat treatment Methods 0.000 claims description 8
150000008104 phosphatidylethanolamines Chemical class 0.000 claims description 8
238000003756 stirring Methods 0.000 claims description 8
-1 phosphatidylcholine hydrogenated phosphatidylcholines Chemical class 0.000 claims description 7
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 7
150000001875 compounds Chemical class 0.000 claims description 6
239000000839 emulsion Substances 0.000 claims description 6
239000002917 insecticide Substances 0.000 claims description 6
239000012141 concentrate Substances 0.000 claims description 5
238000004519 manufacturing process Methods 0.000 claims description 5
238000000034 method Methods 0.000 claims description 5
241000238631 Hexapoda Species 0.000 claims description 4
125000003118 aryl group Chemical group 0.000 claims description 4
LPIQUOYDBNQMRZ-UHFFFAOYSA-N cyclopentene Chemical compound C1CC=CC1 LPIQUOYDBNQMRZ-UHFFFAOYSA-N 0.000 claims description 4
239000000945 filler Substances 0.000 claims description 4
239000011877 solvent mixture Substances 0.000 claims description 4
239000007921 spray Substances 0.000 claims description 4
239000003995 emulsifying agent Substances 0.000 claims description 3
229960000490 permethrin Drugs 0.000 claims description 3
RLLPVAHGXHCWKJ-UHFFFAOYSA-N permethrin Chemical compound CC1(C)C(C=C(Cl)Cl)C1C(=O)OCC1=CC=CC(OC=2C=CC=CC=2)=C1 RLLPVAHGXHCWKJ-UHFFFAOYSA-N 0.000 claims description 3
239000002728 pyrethroid Substances 0.000 claims description 3
239000005946 Cypermethrin Substances 0.000 claims description 2
ATBOMIWRCZXYSZ-XZBBILGWSA-N [1-[2,3-dihydroxypropoxy(hydroxy)phosphoryl]oxy-3-hexadecanoyloxypropan-2-yl] (9e,12e)-octadeca-9,12-dienoate Chemical compound CCCCCCCCCCCCCCCC(=O)OCC(COP(O)(=O)OCC(O)CO)OC(=O)CCCCCCC\C=C\C\C=C\CCCCC ATBOMIWRCZXYSZ-XZBBILGWSA-N 0.000 claims description 2
AWUCVROLDVIAJX-UHFFFAOYSA-N alpha-glycerophosphate Natural products OCC(O)COP(O)(O)=O AWUCVROLDVIAJX-UHFFFAOYSA-N 0.000 claims description 2
239000000969 carrier Substances 0.000 claims description 2
229960005424 cypermethrin Drugs 0.000 claims description 2
KAATUXNTWXVJKI-UHFFFAOYSA-N cypermethrin Chemical compound CC1(C)C(C=C(Cl)Cl)C1C(=O)OC(C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 KAATUXNTWXVJKI-UHFFFAOYSA-N 0.000 claims description 2
229960002483 decamethrin Drugs 0.000 claims description 2
OWZREIFADZCYQD-NSHGMRRFSA-N deltamethrin Chemical compound CC1(C)[C@@H](C=C(Br)Br)[C@H]1C(=O)O[C@H](C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 OWZREIFADZCYQD-NSHGMRRFSA-N 0.000 claims description 2
239000003085 diluting agent Substances 0.000 claims description 2
229910052736 halogen Inorganic materials 0.000 claims description 2
150000002367 halogens Chemical class 0.000 claims description 2
239000008350 hydrogenated phosphatidyl choline Substances 0.000 claims description 2
125000000896 monocarboxylic acid group Chemical group 0.000 claims description 2
RGSFGYAAUTVSQA-UHFFFAOYSA-N pentamethylene Natural products C1CCCC1 RGSFGYAAUTVSQA-UHFFFAOYSA-N 0.000 claims description 2
150000003905 phosphatidylinositols Chemical class 0.000 claims description 2
238000002604 ultrasonography Methods 0.000 claims description 2
239000003960 organic solvent Substances 0.000 claims 3
ASWBNKHCZGQVJV-UHFFFAOYSA-N (3-hexadecanoyloxy-2-hydroxypropyl) 2-(trimethylazaniumyl)ethyl phosphate Chemical compound CCCCCCCCCCCCCCCC(=O)OCC(O)COP([O-])(=O)OCC[N+](C)(C)C ASWBNKHCZGQVJV-UHFFFAOYSA-N 0.000 claims 1
TZCPCKNHXULUIY-RGULYWFUSA-N 1,2-distearoyl-sn-glycero-3-phosphoserine Chemical compound CCCCCCCCCCCCCCCCCC(=O)OC[C@H](COP(O)(=O)OC[C@H](N)C(O)=O)OC(=O)CCCCCCCCCCCCCCCCC TZCPCKNHXULUIY-RGULYWFUSA-N 0.000 claims 1
ZWZWYGMENQVNFU-UHFFFAOYSA-N Glycerophosphorylserin Natural products OC(=O)C(N)COP(O)(=O)OCC(O)CO ZWZWYGMENQVNFU-UHFFFAOYSA-N 0.000 claims 1
229940067605 phosphatidylethanolamines Drugs 0.000 claims 1
PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 12
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 12
HJOVHMDZYOCNQW-UHFFFAOYSA-N isophorone Chemical compound CC1=CC(=O)CC(C)(C)C1 HJOVHMDZYOCNQW-UHFFFAOYSA-N 0.000 description 12
239000008389 polyethoxylated castor oil Substances 0.000 description 7
239000000047 product Substances 0.000 description 7
FIPWRIJSWJWJAI-UHFFFAOYSA-N Butyl carbitol 6-propylpiperonyl ether Chemical compound C1=C(CCC)C(COCCOCCOCCCC)=CC2=C1OCO2 FIPWRIJSWJWJAI-UHFFFAOYSA-N 0.000 description 6
IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 6
229920002685 Polyoxyl 35CastorOil Polymers 0.000 description 6
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
235000011187 glycerol Nutrition 0.000 description 6
QUANRIQJNFHVEU-UHFFFAOYSA-N oxirane;propane-1,2,3-triol Chemical compound C1CO1.OCC(O)CO QUANRIQJNFHVEU-UHFFFAOYSA-N 0.000 description 6
229960005235 piperonyl butoxide Drugs 0.000 description 6
241001465754 Metazoa Species 0.000 description 3
HVVJCLNYMSTOMR-UHFFFAOYSA-N N-(hexanoyl)ethanolamine Chemical compound CCCCCC(=O)NCCO HVVJCLNYMSTOMR-UHFFFAOYSA-N 0.000 description 3
ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
235000014113 dietary fatty acids Nutrition 0.000 description 3
239000000194 fatty acid Substances 0.000 description 3
229930195729 fatty acid Natural products 0.000 description 3
238000005507 spraying Methods 0.000 description 3
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 2
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 2
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
239000003795 chemical substances by application Substances 0.000 description 2
238000004090 dissolution Methods 0.000 description 2
238000009826 distribution Methods 0.000 description 2
230000000694 effects Effects 0.000 description 2
230000005923 long-lasting effect Effects 0.000 description 2
150000008105 phosphatidylcholines Chemical class 0.000 description 2
HYJYGLGUBUDSLJ-UHFFFAOYSA-N pyrethrin Natural products CCC(=O)OC1CC(=C)C2CC3OC3(C)C2C2OC(=O)C(=C)C12 HYJYGLGUBUDSLJ-UHFFFAOYSA-N 0.000 description 2
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 2
235000015112 vegetable and seed oil Nutrition 0.000 description 2
239000008158 vegetable oil Substances 0.000 description 2
239000008096 xylene Substances 0.000 description 2
PEYUIKBAABKQKQ-AFHBHXEDSA-N (+)-sesamin Chemical compound C1=C2OCOC2=CC([C@H]2OC[C@H]3[C@@H]2CO[C@@H]3C2=CC=C3OCOC3=C2)=C1 PEYUIKBAABKQKQ-AFHBHXEDSA-N 0.000 description 1
VSBPRBXTUAKKSY-UHFFFAOYSA-N 5-(5-methyl-1,3-dioxan-4-yl)-1,3-benzodioxole Chemical compound CC1COCOC1C1=CC=C(OCO2)C2=C1 VSBPRBXTUAKKSY-UHFFFAOYSA-N 0.000 description 1
102000009027 Albumins Human genes 0.000 description 1
108010088751 Albumins Proteins 0.000 description 1
239000005995 Aluminium silicate Substances 0.000 description 1
108010076119 Caseins Proteins 0.000 description 1
235000008733 Citrus aurantifolia Nutrition 0.000 description 1
229920000742 Cotton Polymers 0.000 description 1
108010010803 Gelatin Proteins 0.000 description 1
241000208125 Nicotiana Species 0.000 description 1
235000002637 Nicotiana tabacum Nutrition 0.000 description 1
101100269495 Rattus norvegicus Ina gene Proteins 0.000 description 1
WABPPBHOPMUJHV-UHFFFAOYSA-N Sesamex Chemical compound CCOCCOCCOC(C)OC1=CC=C2OCOC2=C1 WABPPBHOPMUJHV-UHFFFAOYSA-N 0.000 description 1
229920002472 Starch Polymers 0.000 description 1
235000011941 Tilia x europaea Nutrition 0.000 description 1
235000012211 aluminium silicate Nutrition 0.000 description 1
230000009286 beneficial effect Effects 0.000 description 1
239000000440 bentonite Substances 0.000 description 1
229910000278 bentonite Inorganic materials 0.000 description 1
235000012216 bentonite Nutrition 0.000 description 1
SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 1
239000012876 carrier material Substances 0.000 description 1
239000005018 casein Substances 0.000 description 1
BECPQYXYKAMYBN-UHFFFAOYSA-N casein, tech. Chemical compound NCCCCC(C(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(CC(C)C)N=C(O)C(CCC(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(C(C)O)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(COP(O)(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(N)CC1=CC=CC=C1 BECPQYXYKAMYBN-UHFFFAOYSA-N 0.000 description 1
235000021240 caseins Nutrition 0.000 description 1
239000007957 coemulsifier Substances 0.000 description 1
239000000084 colloidal system Substances 0.000 description 1
238000004821 distillation Methods 0.000 description 1
244000078703 ectoparasite Species 0.000 description 1
PEYUIKBAABKQKQ-UHFFFAOYSA-N epiasarinin Natural products C1=C2OCOC2=CC(C2OCC3C2COC3C2=CC=C3OCOC3=C2)=C1 PEYUIKBAABKQKQ-UHFFFAOYSA-N 0.000 description 1
150000002168 ethanoic acid esters Chemical class 0.000 description 1
239000012259 ether extract Substances 0.000 description 1
150000004665 fatty acids Chemical class 0.000 description 1
150000002191 fatty alcohols Chemical class 0.000 description 1
235000013312 flour Nutrition 0.000 description 1
238000009472 formulation Methods 0.000 description 1
238000004108 freeze drying Methods 0.000 description 1
229920000159 gelatin Polymers 0.000 description 1
239000008273 gelatin Substances 0.000 description 1
235000019322 gelatine Nutrition 0.000 description 1
235000011852 gelatine desserts Nutrition 0.000 description 1
238000002955 isolation Methods 0.000 description 1
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 1
239000004571 lime Substances 0.000 description 1
239000012263 liquid product Substances 0.000 description 1
231100000053 low toxicity Toxicity 0.000 description 1
229920000609 methyl cellulose Polymers 0.000 description 1
239000001923 methylcellulose Substances 0.000 description 1
239000000546 pharmaceutical excipient Substances 0.000 description 1
125000001095 phosphatidyl group Chemical group 0.000 description 1
230000001681 protective effect Effects 0.000 description 1
229940048383 pyrethrum extract Drugs 0.000 description 1
230000008439 repair process Effects 0.000 description 1
VRMHCMWQHAXTOR-CMOCDZPBSA-N sesamin Natural products C1=C2OCOC2=CC([C@@H]2OC[C@@]3(C)[C@H](C=4C=C5OCOC5=CC=4)OC[C@]32C)=C1 VRMHCMWQHAXTOR-CMOCDZPBSA-N 0.000 description 1
239000000377 silicon dioxide Substances 0.000 description 1
235000012239 silicon dioxide Nutrition 0.000 description 1
229920002545 silicone oil Polymers 0.000 description 1
239000000344 soap Substances 0.000 description 1
239000000243 solution Substances 0.000 description 1
238000001694 spray drying Methods 0.000 description 1
239000003381 stabilizer Substances 0.000 description 1
239000008107 starch Substances 0.000 description 1
235000019698 starch Nutrition 0.000 description 1
239000004575 stone Substances 0.000 description 1
239000000725 suspension Substances 0.000 description 1
230000008961 swelling Effects 0.000 description 1
238000003786 synthesis reaction Methods 0.000 description 1
239000000454 talc Substances 0.000 description 1
229910052623 talc Inorganic materials 0.000 description 1
235000012222 talc Nutrition 0.000 description 1
150000003626 triacylglycerols Chemical class 0.000 description 1
239000000080 wetting agent 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
- A01N57/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds
- A01N57/10—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-oxygen bonds or phosphorus-to-sulfur bonds
- A01N57/12—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-oxygen bonds or phosphorus-to-sulfur bonds containing acyclic or cycloaliphatic radicals

Landscapes

Life Sciences & Earth Sciences (AREA)
Agronomy & Crop Science (AREA)
Pest Control & Pesticides (AREA)
Plant Pathology (AREA)
Health & Medical Sciences (AREA)
Engineering & Computer Science (AREA)
Dentistry (AREA)
General Health & Medical Sciences (AREA)
Wood Science & Technology (AREA)
Zoology (AREA)
Environmental Sciences (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)

NO832456A 1982-07-10 1983-07-05 Insekticid-preparater NO832456L (no)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE19823225943 DE3225943A1 (de)	1982-07-10	1982-07-10	Insektizid-formulierungen

Publications (1)

Publication Number	Publication Date
NO832456L true NO832456L (no)	1984-01-11

Family

ID=6168195

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NO832456A NO832456L (no)	1982-07-10	1983-07-05	Insekticid-preparater

Country Status (15)

Country	Link
EP (1)	EP0099497A1 (fi)
JP (1)	JPS5921606A (fi)
AU (1)	AU1664783A (fi)
BR (1)	BR8303679A (fi)
CS (1)	CS515683A2 (fi)
DD (1)	DD210195A5 (fi)
DE (1)	DE3225943A1 (fi)
DK (1)	DK316383A (fi)
ES (1)	ES523974A0 (fi)
FI (1)	FI832495L (fi)
GR (1)	GR78653B (fi)
NO (1)	NO832456L (fi)
PL (1)	PL242930A3 (fi)
PT (1)	PT77000A (fi)
ZA (1)	ZA834879B (fi)

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US1938864A (en) *	1929-10-21	1933-12-12	Firm Hanseatische Muhlenwerke	Insecticidal emulsion
US2006227A (en) *	1932-10-19	1935-06-25	Grasselli Chemical Co	Contact insecticide
US4241046A (en) *	1978-11-30	1980-12-23	Papahadjopoulos Demetrios P	Method of encapsulating biologically active materials in lipid vesicles
DE3125423A1 (de) *	1981-06-27	1983-01-13	A. Nattermann & Cie GmbH, 5000 Köln	Neue insektizid-zusammensetzung, verfahren zur herstellung und deren verwendung

1982
- 1982-07-10 DE DE19823225943 patent/DE3225943A1/de not_active Withdrawn
1983
- 1983-06-29 GR GR71795A patent/GR78653B/el unknown
- 1983-07-01 EP EP83106402A patent/EP0099497A1/de not_active Withdrawn
- 1983-07-04 ZA ZA834879A patent/ZA834879B/xx unknown
- 1983-07-05 NO NO832456A patent/NO832456L/no unknown
- 1983-07-07 CS CS835156A patent/CS515683A2/cs unknown
- 1983-07-07 AU AU16647/83A patent/AU1664783A/en not_active Abandoned
- 1983-07-07 FI FI832495A patent/FI832495L/fi not_active Application Discontinuation
- 1983-07-08 BR BR8303679A patent/BR8303679A/pt unknown
- 1983-07-08 DK DK316383A patent/DK316383A/da not_active Application Discontinuation
- 1983-07-08 PL PL24293083A patent/PL242930A3/xx unknown
- 1983-07-08 PT PT77000A patent/PT77000A/pt unknown
- 1983-07-08 JP JP58123574A patent/JPS5921606A/ja active Pending
- 1983-07-08 ES ES523974A patent/ES523974A0/es active Granted
- 1983-07-08 DD DD83252905A patent/DD210195A5/de unknown

Also Published As

Publication number	Publication date
CS515683A2 (en)	1985-07-16
GR78653B (fi)	1984-09-27
JPS5921606A (ja)	1984-02-03
BR8303679A (pt)	1984-02-14
DD210195A5 (de)	1984-06-06
DE3225943A1 (de)	1984-01-12
DK316383D0 (da)	1983-07-08
DK316383A (da)	1984-01-11
ZA834879B (en)	1984-03-28
PT77000A (en)	1983-08-01
ES8500006A1 (es)	1984-10-01
FI832495A0 (fi)	1983-07-07
EP0099497A1 (de)	1984-02-01
FI832495L (fi)	1984-01-11
ES523974A0 (es)	1984-10-01
PL242930A3 (en)	1984-07-02
AU1664783A (en)	1985-01-17

Publication	Publication Date	Title
JPH01308206A (ja)	1989-12-12	殺虫、殺ダニ又は殺線虫組成物
EP0215010A1 (en)	1987-03-25	MORE THAN AN INGREDIENT PEST CONTROL COMPOSITION.
CS203967B2 (en)	1981-03-31	Insecticide means
CA1084943A (en)	1980-09-02	Pesticidal m-phenoxybenzyl esters of 2,2- dimethylspiro 2,4 heptane-1-carboxylic acid derivatives
US3472865A (en)	1969-10-14	Substituted benzimidazole compounds
US3414607A (en)	1968-12-03	Novel cyclopropanecarboxylic acid esters
JPH06192279A (ja)	1994-07-12	新規の界面活性剤、これらの製造方法、これらを含有する組成物およびこれらの使用方法
CN104996423A (zh)	2015-10-28	油酸乙酯的用途及油酸乙酯杀螨剂
JPH02225442A (ja)	1990-09-07	３―エテニル―２，２―ジメチルシクロプロパンカルボン酸の新規な弗素化誘導体、その製造方法、害虫駆除剤としてのその使用及びそれを含有する組成物
BRPI0012166B1 (pt)	2015-09-01	Método para combate a pestes selecionadas dentre as ordens isoptera, hymenoptera, orthoptera e psocoptera
NO832456L (no)	1984-01-11	Insekticid-preparater
CA1173744A (en)	1984-09-04	Acaricidal composition, processes for its production and its use
US2350324A (en)	1944-06-06	Parasiticidal composition
JPS5821602B2 (ja)	1983-05-02	殺虫剤組成物
JPS6123161B2 (fi)	1986-06-04
JPH02202806A (ja)	1990-08-10	殺虫、殺ダニ又は殺線虫方法及び殺虫、殺ダニ又は殺線虫剤組成物
JPH05186423A (ja)	1993-07-27	１，３，４，５，６，７−ヘキサヒドロ−１，３−ジオキソ−２ｈ−イソインドール−２−イルメチルアルコールの新規なピレスリノイドエステル、それらの製造法及びそれらのペスチサイドとしての用途
EA000457B1 (ru)	1999-08-26	Пестицидные составы и способ их получения
JPH02164849A (ja)	1990-06-25	殺虫性化合物、その製造方法及びそれを含有する殺虫組成物
US3580716A (en)	1971-05-25	Method for plant growth regulation
JPS60231602A (ja)	1985-11-18	殺菌組成物およびその使用方法
JPH05238906A (ja)	1993-09-17	コナガ防除剤
FR2598408A1 (fr)	1987-11-13	Derives propargyloxybenzenes : leur preparation et compositions fongicides les contenant
US3067091A (en)	1962-12-04	Insect combatting
SU1466635A3 (ru)	1989-03-15	Инсектицидный препарат на основе пиретроидов