NL8400853A - Nieuwe pesticidepreparaten en hun gebruik. - Google Patents

Nieuwe pesticidepreparaten en hun gebruik. Download PDF

Info

Publication number: NL8400853A
Authority: NL; Netherlands
Prior art keywords: inclusion complex; cyclodextrin; growth regulator; insect growth; hydroprene
Prior art date: 1983-03-30

Application number

NL8400853A

Other languages

English (en)

Dutch (nl)

Original Assignee

Sandoz Ag

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.)

1983-03-30

Filing date

1984-03-16

Publication date

1984-10-16

1984-03-16 Application filed by Sandoz Ag filed Critical Sandoz Ag

1984-10-16 Publication of NL8400853A publication Critical patent/NL8400853A/nl

Links

238000002360 preparation method Methods 0.000 title description 6
239000000575 pesticide Substances 0.000 title description 3
241000238631 Hexapoda Species 0.000 claims description 31
229920000858 Cyclodextrin Polymers 0.000 claims description 26
HFHDHCJBZVLPGP-UHFFFAOYSA-N schardinger α-dextrin Chemical compound O1C(C(C2O)O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC(C(O)C2O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC2C(O)C(O)C1OC2CO HFHDHCJBZVLPGP-UHFFFAOYSA-N 0.000 claims description 19
229930000073 hydroprene Natural products 0.000 claims description 18
FYQGBXGJFWXIPP-UHFFFAOYSA-N hydroprene Chemical compound CCOC(=O)C=C(C)C=CCC(C)CCCC(C)C FYQGBXGJFWXIPP-UHFFFAOYSA-N 0.000 claims description 16
239000003630 growth substance Substances 0.000 claims description 15
239000000203 mixture Substances 0.000 claims description 15
229930002897 methoprene Natural products 0.000 claims description 13
229950003442 methoprene Drugs 0.000 claims description 13
NFGXHKASABOEEW-UHFFFAOYSA-N 1-methylethyl 11-methoxy-3,7,11-trimethyl-2,4-dodecadienoate Chemical compound COC(C)(C)CCCC(C)CC=CC(C)=CC(=O)OC(C)C NFGXHKASABOEEW-UHFFFAOYSA-N 0.000 claims description 12
238000000034 method Methods 0.000 claims description 12
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 10
229930001540 kinoprene Natural products 0.000 claims description 8
241001674044 Blattodea Species 0.000 claims description 4
239000003085 diluting agent Substances 0.000 claims description 4
239000011261 inert gas Substances 0.000 claims description 3
230000000749 insecticidal effect Effects 0.000 claims description 3
239000012141 concentrate Substances 0.000 claims description 2
125000003826 hydroprene group Chemical group 0.000 claims 2
238000009472 formulation Methods 0.000 claims 1
238000001802 infusion Methods 0.000 claims 1
125000001665 kinoprene group Chemical group 0.000 claims 1
238000004519 manufacturing process Methods 0.000 claims 1
125000003403 methoprene group Chemical group 0.000 claims 1
239000000843 powder Substances 0.000 description 9
FZRBKIRIBLNOAM-UHFFFAOYSA-N (E,E)-2-propynyl 3,7,11-trimethyl-2,4-dodecadienoate Chemical compound CC(C)CCCC(C)CC=CC(C)=CC(=O)OCC#C FZRBKIRIBLNOAM-UHFFFAOYSA-N 0.000 description 7
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 6
150000001875 compounds Chemical class 0.000 description 6
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 5
241000257303 Hymenoptera Species 0.000 description 5
239000002917 insecticide Substances 0.000 description 5
241000196324 Embryophyta Species 0.000 description 4
239000002949 juvenile hormone Substances 0.000 description 4
239000007787 solid Substances 0.000 description 4
239000001116 FEMA 4028 Substances 0.000 description 3
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
WHGYBXFWUBPSRW-FOUAGVGXSA-N beta-cyclodextrin Chemical compound OC[C@H]([C@H]([C@@H]([C@H]1O)O)O[C@H]2O[C@@H]([C@@H](O[C@H]3O[C@H](CO)[C@H]([C@@H]([C@H]3O)O)O[C@H]3O[C@H](CO)[C@H]([C@@H]([C@H]3O)O)O[C@H]3O[C@H](CO)[C@H]([C@@H]([C@H]3O)O)O[C@H]3O[C@H](CO)[C@H]([C@@H]([C@H]3O)O)O3)[C@H](O)[C@H]2O)CO)O[C@@H]1O[C@H]1[C@H](O)[C@@H](O)[C@@H]3O[C@@H]1CO WHGYBXFWUBPSRW-FOUAGVGXSA-N 0.000 description 3
235000011175 beta-cyclodextrine Nutrition 0.000 description 3
229960004853 betadex Drugs 0.000 description 3
230000000694 effects Effects 0.000 description 3
229910052757 nitrogen Inorganic materials 0.000 description 3
239000003960 organic solvent Substances 0.000 description 3
ROWKJAVDOGWPAT-UHFFFAOYSA-N Acetoin Chemical compound CC(O)C(C)=O ROWKJAVDOGWPAT-UHFFFAOYSA-N 0.000 description 2
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
239000005995 Aluminium silicate Substances 0.000 description 2
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
102000004190 Enzymes Human genes 0.000 description 2
108090000790 Enzymes Proteins 0.000 description 2
241000258937 Hemiptera Species 0.000 description 2
235000012211 aluminium silicate Nutrition 0.000 description 2
229940097362 cyclodextrins Drugs 0.000 description 2
238000001704 evaporation Methods 0.000 description 2
235000013312 flour Nutrition 0.000 description 2
235000013305 food Nutrition 0.000 description 2
239000002418 insect attractant 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
239000007788 liquid Substances 0.000 description 2
229920001592 potato starch Polymers 0.000 description 2
230000035484 reaction time Effects 0.000 description 2
238000003756 stirring Methods 0.000 description 2
239000000126 substance Substances 0.000 description 2
239000000454 talc Substances 0.000 description 2
229910052623 talc Inorganic materials 0.000 description 2
239000005418 vegetable material Substances 0.000 description 2
239000004563 wettable powder Substances 0.000 description 2
RLLPVAHGXHCWKJ-IEBWSBKVSA-N (3-phenoxyphenyl)methyl (1s,3s)-3-(2,2-dichloroethenyl)-2,2-dimethylcyclopropane-1-carboxylate Chemical compound CC1(C)[C@H](C=C(Cl)Cl)[C@@H]1C(=O)OCC1=CC=CC(OC=2C=CC=CC=2)=C1 RLLPVAHGXHCWKJ-IEBWSBKVSA-N 0.000 description 1
XOGODJOZAUTXDH-UHFFFAOYSA-M (N-methylanilino)methanesulfonate Chemical group CN(CS([O-])(=O)=O)c1ccccc1 XOGODJOZAUTXDH-UHFFFAOYSA-M 0.000 description 1
239000004382 Amylase Substances 0.000 description 1
102000013142 Amylases Human genes 0.000 description 1
108010065511 Amylases Proteins 0.000 description 1
235000017060 Arachis glabrata Nutrition 0.000 description 1
244000105624 Arachis hypogaea Species 0.000 description 1
235000010777 Arachis hypogaea Nutrition 0.000 description 1
235000018262 Arachis monticola Nutrition 0.000 description 1
241000282472 Canis lupus familiaris Species 0.000 description 1
241001121020 Cetonia aurata Species 0.000 description 1
229920002261 Corn starch Polymers 0.000 description 1
229920001353 Dextrin Polymers 0.000 description 1
239000004375 Dextrin Substances 0.000 description 1
241000282324 Felis Species 0.000 description 1
241000282326 Felis catus Species 0.000 description 1
244000017020 Ipomoea batatas Species 0.000 description 1
235000002678 Ipomoea batatas Nutrition 0.000 description 1
239000005909 Kieselgur Substances 0.000 description 1
229920001732 Lignosulfonate Polymers 0.000 description 1
241001465754 Metazoa Species 0.000 description 1
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
229910019142 PO4 Inorganic materials 0.000 description 1
241000178960 Paenibacillus macerans Species 0.000 description 1
ISRUGXGCCGIOQO-UHFFFAOYSA-N Rhoden Chemical compound CNC(=O)OC1=CC=CC=C1OC(C)C ISRUGXGCCGIOQO-UHFFFAOYSA-N 0.000 description 1
DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 description 1
INISTDXBRIBGOC-CGAIIQECSA-N [cyano-(3-phenoxyphenyl)methyl] (2s)-2-[2-chloro-4-(trifluoromethyl)anilino]-3-methylbutanoate Chemical compound N([C@@H](C(C)C)C(=O)OC(C#N)C=1C=C(OC=2C=CC=CC=2)C=CC=1)C1=CC=C(C(F)(F)F)C=C1Cl INISTDXBRIBGOC-CGAIIQECSA-N 0.000 description 1
230000002159 abnormal effect Effects 0.000 description 1
150000001298 alcohols Chemical class 0.000 description 1
235000019418 amylase Nutrition 0.000 description 1
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 description 1
150000004657 carbamic acid derivatives Chemical class 0.000 description 1
CVXBEEMKQHEXEN-UHFFFAOYSA-N carbaryl Chemical compound C1=CC=C2C(OC(=O)NC)=CC=CC2=C1 CVXBEEMKQHEXEN-UHFFFAOYSA-N 0.000 description 1
229960005286 carbaryl Drugs 0.000 description 1
238000001816 cooling Methods 0.000 description 1
239000008120 corn starch Substances 0.000 description 1
230000009193 crawling Effects 0.000 description 1
230000018109 developmental process Effects 0.000 description 1
235000019425 dextrin Nutrition 0.000 description 1
OEBRKCOSUFCWJD-UHFFFAOYSA-N dichlorvos Chemical compound COP(=O)(OC)OC=C(Cl)Cl OEBRKCOSUFCWJD-UHFFFAOYSA-N 0.000 description 1
229950001327 dichlorvos Drugs 0.000 description 1
239000000428 dust Substances 0.000 description 1
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
230000008020 evaporation Effects 0.000 description 1
238000000855 fermentation Methods 0.000 description 1
230000004151 fermentation Effects 0.000 description 1
GFAZHVHNLUBROE-UHFFFAOYSA-N hydroxymethyl propionaldehyde Natural products CCC(=O)CO GFAZHVHNLUBROE-UHFFFAOYSA-N 0.000 description 1
239000004615 ingredient Substances 0.000 description 1
239000000077 insect repellent Substances 0.000 description 1
230000003993 interaction Effects 0.000 description 1
229930014550 juvenile hormone Natural products 0.000 description 1
150000003633 juvenile hormone derivatives Chemical class 0.000 description 1
230000029052 metamorphosis Effects 0.000 description 1
BUYMVQAILCEWRR-UHFFFAOYSA-N naled Chemical compound COP(=O)(OC)OC(Br)C(Cl)(Cl)Br BUYMVQAILCEWRR-UHFFFAOYSA-N 0.000 description 1
239000002245 particle Substances 0.000 description 1
235000020232 peanut Nutrition 0.000 description 1
235000021317 phosphate Nutrition 0.000 description 1
150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
102000004169 proteins and genes Human genes 0.000 description 1
108090000623 proteins and genes Proteins 0.000 description 1
239000005871 repellent Substances 0.000 description 1
230000002940 repellent Effects 0.000 description 1
VEMKTZHHVJILDY-UHFFFAOYSA-N resmethrin Chemical compound CC1(C)C(C=C(C)C)C1C(=O)OCC1=COC(CC=2C=CC=CC=2)=C1 VEMKTZHHVJILDY-UHFFFAOYSA-N 0.000 description 1
239000000377 silicon dioxide Substances 0.000 description 1
235000012239 silicon dioxide Nutrition 0.000 description 1
235000019333 sodium laurylsulphate Nutrition 0.000 description 1
239000002689 soil Substances 0.000 description 1
239000002904 solvent Substances 0.000 description 1
238000005507 spraying Methods 0.000 description 1
239000004094 surface-active agent Substances 0.000 description 1
239000000725 suspension Substances 0.000 description 1
239000008096 xylene Substances 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08B—POLYSACCHARIDES; DERIVATIVES THEREOF
- C08B37/00—Preparation of polysaccharides not provided for in groups C08B1/00 - C08B35/00; Derivatives thereof
- C08B37/0006—Homoglycans, i.e. polysaccharides having a main chain consisting of one single sugar, e.g. colominic acid
- C08B37/0009—Homoglycans, i.e. polysaccharides having a main chain consisting of one single sugar, e.g. colominic acid alpha-D-Glucans, e.g. polydextrose, alternan, glycogen; (alpha-1,4)(alpha-1,6)-D-Glucans; (alpha-1,3)(alpha-1,4)-D-Glucans, e.g. isolichenan or nigeran; (alpha-1,4)-D-Glucans; (alpha-1,3)-D-Glucans, e.g. pseudonigeran; Derivatives thereof
- C08B37/0012—Cyclodextrin [CD], e.g. cycle with 6 units (alpha), with 7 units (beta) and with 8 units (gamma), large-ring cyclodextrin or cycloamylose with 9 units or more; Derivatives thereof
- C08B37/0015—Inclusion compounds, i.e. host-guest compounds, e.g. polyrotaxanes
- 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
- A01N25/08—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 solids as carriers or diluents
- A01N25/10—Macromolecular compounds
- 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
- A01N49/00—Biocides, pest repellants or attractants, or plant growth regulators, containing compounds containing the group, wherein m+n>=1, both X together may also mean —Y— or a direct carbon-to-carbon bond, and the carbon atoms marked with an asterisk are not part of any ring system other than that which may be formed by the atoms X, the carbon atoms in square brackets being part of any acyclic or cyclic structure, or the group, wherein A means a carbon atom or Y, n>=0, and not more than one of these carbon atoms being a member of the same ring system, e.g. juvenile insect hormones or mimics thereof

Landscapes

Life Sciences & Earth Sciences (AREA)
Health & Medical Sciences (AREA)
General Health & Medical Sciences (AREA)
Engineering & Computer Science (AREA)
Chemical & Material Sciences (AREA)
Zoology (AREA)
Agronomy & Crop Science (AREA)
Environmental Sciences (AREA)
Wood Science & Technology (AREA)
Dentistry (AREA)
Plant Pathology (AREA)
Pest Control & Pesticides (AREA)
Polymers & Plastics (AREA)
Organic Chemistry (AREA)
Biochemistry (AREA)
Toxicology (AREA)
Medicinal Chemistry (AREA)
Chemical Kinetics & Catalysis (AREA)
Molecular Biology (AREA)
Materials Engineering (AREA)
Insects & Arthropods (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Polysaccharides And Polysaccharide Derivatives (AREA)

NL8400853A 1983-03-30 1984-03-16 Nieuwe pesticidepreparaten en hun gebruik. NL8400853A (nl)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
US48053483A	1983-03-30	1983-03-30
US48053483		1983-03-30

Publications (1)

Publication Number	Publication Date
NL8400853A true NL8400853A (nl)	1984-10-16

Family

ID=23908333

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NL8400853A NL8400853A (nl)	1983-03-30	1984-03-16	Nieuwe pesticidepreparaten en hun gebruik.

Country Status (16)

Country	Link
JP (1)	JPS59219202A (es)
AT (1)	ATA105684A (es)
AU (1)	AU2617684A (es)
BE (1)	BE899252A (es)
CH (1)	CH660193A5 (es)
DE (1)	DE3410319A1 (es)
DK (1)	DK171984A (es)
ES (1)	ES531056A0 (es)
FR (1)	FR2543403B1 (es)
GB (1)	GB2138293B (es)
HU (1)	HUT37857A (es)
IL (1)	IL71381A (es)
IT (1)	IT1199099B (es)
NL (1)	NL8400853A (es)
TR (1)	TR22227A (es)
ZA (1)	ZA842435B (es)

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
GB2162529B (en) *	1984-06-08	1988-03-02	Nitrokemia Ipartelepek	B-cyclodextrin complex of benzene sulphonyl urea derivatives
JPS61152765A (ja) *	1984-12-27	1986-07-11	Nippon Ekishiyou Kk	シクロデキストリン類で包接された化合物を含有した合成樹脂製品及びその製造方法
FR2596617B1 (fr) *	1986-04-08	1990-10-05	Orstom	Composition a base d'acide gras complexe par des cyclodextrines, son procede de preparation et application phytosanitaire
HUT49447A (en) *	1988-03-17	1989-10-30	Chinoin Gyogyszer Es Vegyeszet	Process for producing stabil acaricide amitrase-composition
ZA903739B (en) *	1989-05-27	1991-03-27	Sumitomo Chemical Co	A poison bait for control of noxious insects
JP2974373B2 (ja) *	1989-05-27	1999-11-10	住友化学工業株式会社	害虫駆除用毒餌剤
US6663876B2 (en)	2002-04-29	2003-12-16	Piedmont Pharmaceuticals, Llc	Methods and compositions for treating ectoparasite infestation
CN1232539C (zh) *	2002-05-10	2005-12-21	刘云清	有机药物与倍他环糊精衍生物的配合物及其制备方法
ES2417380B1 (es) *	2012-01-05	2014-06-03	Universidad Del Pais Vasco - Euskal Herriko Unibertsitatea	Nuevos complejos de inclusión de pesticidas, composiciones que los contienen y su empleo como pesticidas

Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE895769C (de) *	1951-08-26	1953-11-05	Knoll Ag	Verfahren zur Herstellung von Einschlussverbindungen physiologisch wirksamer organischer Verbindungen
US3130121A (en) *	1961-02-10	1964-04-21	Leeco Chemican Company Divisio	Insecticidal powder
DE1542902A1 (de) *	1964-05-21	1970-04-16	Harvest Queen Mill & Elevator	Als Biozid geeignetes,emulgierbares Pulverkonzentrat
US4021461A (en) *	1971-11-22	1977-05-03	Zoecon Corporation	Aliphatic hydrocarbon 2,4-dienoic acids, esters and derivatives thereof
US3904662A (en) *	1972-02-07	1975-09-09	Zoecon Corp	2,4-dienoic acids, esters and derivatives
JPS5017529B2 (es) *	1972-11-20	1975-06-21
JPS5745722B2 (es) *	1973-07-27	1982-09-29
JPS5761261B2 (es) *	1975-01-17	1982-12-23	Dainippon Jochugiku Kk
US4230687A (en) *	1978-05-30	1980-10-28	Griffith Laboratories U.S.A., Inc.	Encapsulation of active agents as microdispersions in homogeneous natural polymeric matrices

1984
- 1984-03-16 HU HU841058A patent/HUT37857A/hu unknown
- 1984-03-16 NL NL8400853A patent/NL8400853A/nl not_active Application Discontinuation
- 1984-03-21 DE DE19843410319 patent/DE3410319A1/de not_active Ceased
- 1984-03-26 TR TR22227A patent/TR22227A/xx unknown
- 1984-03-27 GB GB08407909A patent/GB2138293B/en not_active Expired
- 1984-03-27 BE BE1/10989A patent/BE899252A/fr not_active IP Right Cessation
- 1984-03-27 CH CH1522/84A patent/CH660193A5/de not_active IP Right Cessation
- 1984-03-27 FR FR848404887A patent/FR2543403B1/fr not_active Expired - Lifetime
- 1984-03-28 DK DK171984A patent/DK171984A/da not_active IP Right Cessation
- 1984-03-28 AU AU26176/84A patent/AU2617684A/en not_active Abandoned
- 1984-03-28 IL IL71381A patent/IL71381A/xx not_active IP Right Cessation
- 1984-03-28 ES ES531056A patent/ES531056A0/es active Granted
- 1984-03-29 AT AT0105684A patent/ATA105684A/de not_active IP Right Cessation
- 1984-03-29 JP JP59063121A patent/JPS59219202A/ja active Granted
- 1984-03-29 IT IT47964/84A patent/IT1199099B/it active
- 1984-03-30 ZA ZA842435A patent/ZA842435B/xx unknown

Also Published As

Publication number	Publication date
AU2617684A (en)	1984-10-04
GB2138293A (en)	1984-10-24
DK171984D0 (da)	1984-03-28
JPH0572361B2 (es)	1993-10-12
ES8507574A1 (es)	1985-09-16
IL71381A (en)	1987-09-16
DK171984A (da)	1984-10-01
GB8407909D0 (en)	1984-05-02
HUT37857A (en)	1986-03-28
ATA105684A (de)	1988-10-15
TR22227A (tr)	1986-10-09
FR2543403A1 (fr)	1984-10-05
IT1199099B (it)	1988-12-30
ZA842435B (en)	1985-11-27
CH660193A5 (de)	1987-03-31
JPS59219202A (ja)	1984-12-10
IT8447964A0 (it)	1984-03-29
ES531056A0 (es)	1985-09-16
GB2138293B (en)	1986-07-02
BE899252A (fr)	1984-09-27
IT8447964A1 (it)	1985-09-29
FR2543403B1 (fr)	1990-01-26
DE3410319A1 (de)	1984-12-13

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CN100525614C (zh)	2009-08-12	害虫防治剂载体
NL8400853A (nl)	1984-10-16	Nieuwe pesticidepreparaten en hun gebruik.
JP3580591B2 (ja)	2004-10-27	殺虫組成物
US7445791B2 (en)	2008-11-04	Synergistic insecticidal composition containing Chloronicotynyle and Organosphosphorus compounds
KR100753263B1 (ko)	2007-08-29	유기 화합물
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