CS227687B2 - Insecticide and acaricide - Google Patents

Insecticide and acaricide Download PDF

Info

Publication number: CS227687B2
Authority: CS; Czechoslovakia
Prior art keywords: compound; formula; active; group; compounds
Prior art date: 1981-05-02

Application number

CS823127A

Other languages

Czech (cs)

English (en)

Inventor

Werner Dr Knauf

Gerhard Dr Salbeck

Anna Dr Waltersdorfer

Original Assignee

Hoechst 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.)

1981-05-02

Filing date

1982-04-30

Publication date

1984-05-14

1982-04-30 Application filed by Hoechst Ag filed Critical Hoechst Ag

1984-05-14 Publication of CS227687B2 publication Critical patent/CS227687B2/cs

Links

230000000895 acaricidal effect Effects 0.000 title claims description 4
239000002917 insecticide Substances 0.000 title description 2
239000000642 acaricide Substances 0.000 title 1
150000001875 compounds Chemical class 0.000 claims abstract description 55
229910052739 hydrogen Inorganic materials 0.000 claims abstract description 5
239000001257 hydrogen Substances 0.000 claims abstract description 5
125000004093 cyano group Chemical group *C#N 0.000 claims abstract description 3
239000000203 mixture Substances 0.000 claims description 31
239000004480 active ingredient Substances 0.000 claims description 18
-1 dichlorovinyl Chemical group 0.000 claims description 17
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 5
125000000217 alkyl group Chemical group 0.000 claims description 3
230000000749 insecticidal effect Effects 0.000 claims description 3
125000001309 chloro group Chemical group Cl* 0.000 claims description 2
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 2
230000003287 optical effect Effects 0.000 claims description 2
LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 claims description 2
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 2
241000238631 Hexapoda Species 0.000 abstract description 7
241000238876 Acari Species 0.000 abstract description 4
238000000034 method Methods 0.000 abstract description 4
125000006273 (C1-C3) alkyl group Chemical group 0.000 abstract description 3
239000003795 chemical substances by application Substances 0.000 abstract description 3
230000000361 pesticidal effect Effects 0.000 abstract description 2
229910052736 halogen Inorganic materials 0.000 abstract 3
150000002367 halogens Chemical class 0.000 abstract 3
JCXJVPUVTGWSNB-UHFFFAOYSA-N Nitrogen dioxide Chemical compound O=[N]=O JCXJVPUVTGWSNB-UHFFFAOYSA-N 0.000 abstract 1
HSFWRNGVRCDJHI-UHFFFAOYSA-N alpha-acetylene Natural products C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 0.000 abstract 1
125000003710 aryl alkyl group Chemical group 0.000 abstract 1
125000001769 aryl amino group Chemical group 0.000 abstract 1
125000004104 aryloxy group Chemical group 0.000 abstract 1
125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 abstract 1
125000002534 ethynyl group Chemical group [H]C#C* 0.000 abstract 1
150000002431 hydrogen Chemical class 0.000 abstract 1
125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 abstract 1
229910052760 oxygen Inorganic materials 0.000 abstract 1
229910052717 sulfur Inorganic materials 0.000 abstract 1
239000013543 active substance Substances 0.000 description 15
239000000243 solution Substances 0.000 description 13
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 8
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 8
238000002360 preparation method Methods 0.000 description 8
239000000843 powder Substances 0.000 description 7
238000010790 dilution Methods 0.000 description 6
239000012895 dilution Substances 0.000 description 6
230000000694 effects Effects 0.000 description 6
239000000725 suspension Substances 0.000 description 6
241000607479 Yersinia pestis Species 0.000 description 5
239000002253 acid Substances 0.000 description 5
239000007921 spray Substances 0.000 description 5
241000239290 Araneae Species 0.000 description 4
238000009472 formulation Methods 0.000 description 4
239000007787 solid Substances 0.000 description 4
239000000126 substance Substances 0.000 description 4
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 3
GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 3
239000000853 adhesive Substances 0.000 description 3
230000001070 adhesive effect Effects 0.000 description 3
159000000007 calcium salts Chemical class 0.000 description 3
239000000969 carrier Substances 0.000 description 3
239000012141 concentrate Substances 0.000 description 3
239000004495 emulsifiable concentrate Substances 0.000 description 3
239000003337 fertilizer Substances 0.000 description 3
239000008187 granular material Substances 0.000 description 3
239000007788 liquid Substances 0.000 description 3
238000002156 mixing Methods 0.000 description 3
239000000047 product Substances 0.000 description 3
239000000377 silicon dioxide Substances 0.000 description 3
230000002195 synergetic effect Effects 0.000 description 3
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
241000254175 Anthonomus grandis Species 0.000 description 2
241001124076 Aphididae Species 0.000 description 2
241000238659 Blatta Species 0.000 description 2
241001674044 Blattodea Species 0.000 description 2
241000254173 Coleoptera Species 0.000 description 2
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
241000257159 Musca domestica Species 0.000 description 2
LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
244000046052 Phaseolus vulgaris Species 0.000 description 2
241001454295 Tetranychidae Species 0.000 description 2
244000038559 crop plants Species 0.000 description 2
HGCIXCUEYOPUTN-UHFFFAOYSA-N cyclohexene Chemical compound C1CCC=CC1 HGCIXCUEYOPUTN-UHFFFAOYSA-N 0.000 description 2
235000014113 dietary fatty acids Nutrition 0.000 description 2
239000006185 dispersion Substances 0.000 description 2
238000004090 dissolution Methods 0.000 description 2
239000003995 emulsifying agent Substances 0.000 description 2
LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
239000000194 fatty acid Substances 0.000 description 2
229930195729 fatty acid Natural products 0.000 description 2
239000000945 filler Substances 0.000 description 2
229930195733 hydrocarbon Natural products 0.000 description 2
150000002430 hydrocarbons Chemical class 0.000 description 2
125000004435 hydrogen atom Chemical group [H]* 0.000 description 2
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 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
230000001418 larval effect Effects 0.000 description 2
125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 description 2
150000003839 salts Chemical class 0.000 description 2
239000002904 solvent Substances 0.000 description 2
241000894007 species Species 0.000 description 2
230000001988 toxicity Effects 0.000 description 2
231100000419 toxicity Toxicity 0.000 description 2
XJRIDJAGAYGJCK-UHFFFAOYSA-N (1-acetyl-5-bromoindol-3-yl) acetate Chemical compound C1=C(Br)C=C2C(OC(=O)C)=CN(C(C)=O)C2=C1 XJRIDJAGAYGJCK-UHFFFAOYSA-N 0.000 description 1
WBIQQQGBSDOWNP-UHFFFAOYSA-N 2-dodecylbenzenesulfonic acid Chemical class CCCCCCCCCCCCC1=CC=CC=C1S(O)(=O)=O WBIQQQGBSDOWNP-UHFFFAOYSA-N 0.000 description 1
241001136265 Agriotes Species 0.000 description 1
239000005995 Aluminium silicate Substances 0.000 description 1
241000952611 Aphis craccivora Species 0.000 description 1
244000075850 Avena orientalis Species 0.000 description 1
235000007319 Avena orientalis Nutrition 0.000 description 1
241000238662 Blatta orientalis Species 0.000 description 1
241000238657 Blattella germanica Species 0.000 description 1
241000256593 Brachycaudus schwartzi Species 0.000 description 1
OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
241001249699 Capitata Species 0.000 description 1
239000004215 Carbon black (E152) Substances 0.000 description 1
FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 1
FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 1
241000462639 Epilachna varivestis Species 0.000 description 1
VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
244000068988 Glycine max Species 0.000 description 1
235000010469 Glycine max Nutrition 0.000 description 1
DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
239000005909 Kieselgur Substances 0.000 description 1
241000258915 Leptinotarsa Species 0.000 description 1
241000258916 Leptinotarsa decemlineata Species 0.000 description 1
QENGPZGAWFQWCZ-UHFFFAOYSA-N Methylthiophene Natural products CC=1C=CSC=1 QENGPZGAWFQWCZ-UHFFFAOYSA-N 0.000 description 1
241000721623 Myzus Species 0.000 description 1
XPXQNLGCXHTHNN-MDTVQASCSA-N N[C@@H](CCCCN)C(=O)O.N[C@@H](CCCCN)C(=O)O.[Na] Chemical compound N[C@@H](CCCCN)C(=O)O.N[C@@H](CCCCN)C(=O)O.[Na] XPXQNLGCXHTHNN-MDTVQASCSA-N 0.000 description 1
GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Polymers O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 1
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
241000488581 Panonychus citri Species 0.000 description 1
241000488583 Panonychus ulmi Species 0.000 description 1
240000001090 Papaver somniferum Species 0.000 description 1
235000008753 Papaver somniferum Nutrition 0.000 description 1
241000562493 Pegomya Species 0.000 description 1
241000275067 Phyllotreta Species 0.000 description 1
229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
235000005805 Prunus cerasus Nutrition 0.000 description 1
241000254105 Tenebrio Species 0.000 description 1
241001454294 Tetranychus Species 0.000 description 1
241001454293 Tetranychus urticae Species 0.000 description 1
240000006677 Vicia faba Species 0.000 description 1
235000010749 Vicia faba Nutrition 0.000 description 1
USNWAMPROKAEIT-UHFFFAOYSA-N [Na].C(C=C)(=O)O Chemical compound [Na].C(C=C)(=O)O USNWAMPROKAEIT-UHFFFAOYSA-N 0.000 description 1
230000002745 absorbent Effects 0.000 description 1
239000002250 absorbent Substances 0.000 description 1
150000001241 acetals Chemical class 0.000 description 1
150000007513 acids Chemical class 0.000 description 1
230000000274 adsorptive effect Effects 0.000 description 1
150000001298 alcohols Chemical class 0.000 description 1
235000012211 aluminium silicate Nutrition 0.000 description 1
230000008485 antagonism Effects 0.000 description 1
239000007900 aqueous suspension Substances 0.000 description 1
239000012752 auxiliary agent Substances 0.000 description 1
239000000440 bentonite Substances 0.000 description 1
229910000278 bentonite Inorganic materials 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
UHOVQNZJYSORNB-UHFFFAOYSA-N benzene Substances C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 1
239000011230 binding agent Substances 0.000 description 1
230000003115 biocidal effect Effects 0.000 description 1
238000009835 boiling Methods 0.000 description 1
239000011575 calcium Substances 0.000 description 1
229910052791 calcium Inorganic materials 0.000 description 1
239000000460 chlorine Substances 0.000 description 1
229910052801 chlorine Inorganic materials 0.000 description 1
230000002301 combined effect Effects 0.000 description 1
239000007859 condensation product Substances 0.000 description 1
238000013270 controlled release Methods 0.000 description 1
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 description 1
239000003085 diluting agent Substances 0.000 description 1
238000003113 dilution method Methods 0.000 description 1
239000002270 dispersing agent Substances 0.000 description 1
238000001035 drying Methods 0.000 description 1
239000000839 emulsion Substances 0.000 description 1
238000001704 evaporation Methods 0.000 description 1
230000008020 evaporation Effects 0.000 description 1
239000002360 explosive Substances 0.000 description 1
150000002191 fatty alcohols Chemical class 0.000 description 1
239000000417 fungicide Substances 0.000 description 1
238000000227 grinding Methods 0.000 description 1
239000004009 herbicide Substances 0.000 description 1
239000004615 ingredient Substances 0.000 description 1
230000001050 lubricating effect Effects 0.000 description 1
238000004519 manufacturing process Methods 0.000 description 1
239000000463 material Substances 0.000 description 1
238000002844 melting Methods 0.000 description 1
230000008018 melting Effects 0.000 description 1
MYWUZJCMWCOHBA-VIFPVBQESA-N methamphetamine Chemical compound CN[C@@H](C)CC1=CC=CC=C1 MYWUZJCMWCOHBA-VIFPVBQESA-N 0.000 description 1
239000002480 mineral oil Substances 0.000 description 1
239000004570 mortar (masonry) Substances 0.000 description 1
210000003097 mucus Anatomy 0.000 description 1
239000003960 organic solvent Substances 0.000 description 1
239000003090 pesticide formulation Substances 0.000 description 1
229920000570 polyether Polymers 0.000 description 1
239000010453 quartz Substances 0.000 description 1
239000002002 slurry Substances 0.000 description 1
239000011734 sodium Substances 0.000 description 1
229910052708 sodium Inorganic materials 0.000 description 1
159000000000 sodium salts Chemical class 0.000 description 1
239000002689 soil Substances 0.000 description 1
239000000600 sorbitol Substances 0.000 description 1
238000005507 spraying Methods 0.000 description 1
239000000454 talc Substances 0.000 description 1
229910052623 talc Inorganic materials 0.000 description 1
229920002554 vinyl polymer Polymers 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
- A01N57/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds
- A01N57/18—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-carbon bonds
- A01N57/22—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-carbon bonds containing aromatic 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)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

CS823127A 1981-05-02 1982-04-30 Insecticide and acaricide CS227687B2 (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE19813117435 DE3117435A1 (de)	1981-05-02	1981-05-02	Schaedlingsbekaempfungsmittel

Publications (1)

Publication Number	Publication Date
CS227687B2 true CS227687B2 (en)	1984-05-14

Family

ID=6131325

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CS823127A CS227687B2 (en)	1981-05-02	1982-04-30	Insecticide and acaricide

Country Status (16)

Country	Link
EP (1)	EP0064670A1 (fr)
JP (1)	JPS57209205A (fr)
AU (1)	AU8317382A (fr)
BR (1)	BR8202522A (fr)
CS (1)	CS227687B2 (fr)
DD (1)	DD202380A5 (fr)
DE (1)	DE3117435A1 (fr)
DK (1)	DK195282A (fr)
ES (1)	ES8405245A1 (fr)
GR (1)	GR75427B (fr)
IL (1)	IL65655A0 (fr)
MA (1)	MA19457A1 (fr)
OA (1)	OA07088A (fr)
PL (1)	PL236240A1 (fr)
ZA (1)	ZA822979B (fr)
ZW (1)	ZW8882A1 (fr)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
RU2087477C1 (ru) *	1995-06-30	1997-08-20	Институт элементоорганических соединений РАН	0,0-диалкил-s-[(n-алкокси(арокси)карбонил-n-алкоксикарбонилалкил)аминометил]ди(моно)тиофосфаты, проявляющие синергистическое действие к периметру в отношении комнатных мух и синатропных тараканов

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE2617736C2 (de) *	1976-04-23	1982-12-09	Hoechst Ag, 6000 Frankfurt	Schädlingsbekämpfungsmittel

1981
- 1981-05-02 DE DE19813117435 patent/DE3117435A1/de not_active Withdrawn
1982
- 1982-04-21 MA MA19662A patent/MA19457A1/fr unknown
- 1982-04-26 ES ES511710A patent/ES8405245A1/es not_active Expired
- 1982-04-28 EP EP82103619A patent/EP0064670A1/fr not_active Withdrawn
- 1982-04-28 DD DD82239382A patent/DD202380A5/de unknown
- 1982-04-30 OA OA57674A patent/OA07088A/fr unknown
- 1982-04-30 ZA ZA822979A patent/ZA822979B/xx unknown
- 1982-04-30 JP JP57071625A patent/JPS57209205A/ja active Pending
- 1982-04-30 GR GR68036A patent/GR75427B/el unknown
- 1982-04-30 PL PL23624082A patent/PL236240A1/xx unknown
- 1982-04-30 BR BR8202522A patent/BR8202522A/pt unknown
- 1982-04-30 AU AU83173/82A patent/AU8317382A/en not_active Abandoned
- 1982-04-30 DK DK195282A patent/DK195282A/da not_active Application Discontinuation
- 1982-04-30 ZW ZW88/82A patent/ZW8882A1/xx unknown
- 1982-04-30 IL IL65655A patent/IL65655A0/xx unknown
- 1982-04-30 CS CS823127A patent/CS227687B2/cs unknown

Also Published As

Publication number	Publication date
ZA822979B (en)	1983-03-30
GR75427B (fr)	1984-07-17
BR8202522A (pt)	1983-04-19
PL236240A1 (fr)	1982-12-06
MA19457A1 (fr)	1982-12-31
ES511710A0 (es)	1983-10-01
DE3117435A1 (de)	1982-11-18
DD202380A5 (de)	1983-09-14
OA07088A (fr)	1984-01-31
ES8405245A1 (es)	1983-10-01
EP0064670A1 (fr)	1982-11-17
IL65655A0 (en)	1982-07-30
DK195282A (da)	1982-11-03
JPS57209205A (en)	1982-12-22
ZW8882A1 (en)	1982-11-24
AU8317382A (en)	1982-11-11

Publication	Publication Date	Title
PL94954B1 (fr)	1977-09-30
JP3086924B2 (ja)	2000-09-11	殺虫組成物
CS227693B2 (en)	1984-05-14	Insecticide and method of its preparation
JP3495056B2 (ja)	2004-02-09	殺虫組成物
PL105939B1 (pl)	1979-11-30	Srodek owadobojczy i roztoczobojczy
PL95242B1 (fr)	1977-09-30
CS227687B2 (en)	1984-05-14	Insecticide and acaricide
KR0179660B1 (ko)	1999-04-01	살충 및 살진균제
US4889867A (en)	1989-12-26	Photoactivated miticidal and insecticidal ethynyl-thiazoles
JPH02229157A (ja)	1990-09-11	テトラヒドロフタルイミド誘導体および除草剤
PL136866B1 (en)	1986-03-31	Pecticide and process for manufacturing aryl esters of n-oxalyl-n-methylcarbamic acid
EP0065216A1 (fr)	1982-11-24	S-(triazol-1.2.4-yl-5-méthyl-) (di)-thiophosph(on)ates et procédé pour les préparer
JPH01153671A (ja)	1989-06-15	新規チオイミデート及びアミジン殺虫剤
KR20010031088A (ko)	2001-04-16	4-아릴-4-치환피라졸리딘-3,5-디온 유도체
JP2871113B2 (ja)	1999-03-17	除草用組成物
US4103007A (en)	1978-07-25	Pesticidal synergistic mixture of a dioxathiepin and a formamidine
KR0174374B1 (ko)	1999-02-18	벤조페논옥심에스테르 구조를 갖는 제초성 피리미딘화합물 및 그의 제조방법
KR840001148B1 (ko)	1984-08-11	티아졸일리덴-옥소-프로피오니트릴의 제조방법
KR100330692B1 (ko)	2005-01-10	농업용 살충 및 살진균 조성물
DE3203656A1 (de)	1983-08-11	Neue 1,2,3-thiadiazolymethyl-(di)thiophosphate, -phosphonate und phosphoramidate, verfahren zu ihrer herstellung, diese enthaltende mittel und deren verwendung als pestizide sowie neue thiadiazole als zwischenstufen und verfahren zu deren herstellung
JPS63156705A (ja)	1988-06-29	農業用殺虫殺菌剤組成物
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