BG60284B2 - Артроподен препарат - Google Patents
Артроподен препарат Download PDFInfo
- Publication number
- BG60284B2 BG60284B2 BG087126A BG8712689A BG60284B2 BG 60284 B2 BG60284 B2 BG 60284B2 BG 087126 A BG087126 A BG 087126A BG 8712689 A BG8712689 A BG 8712689A BG 60284 B2 BG60284 B2 BG 60284B2
- Authority
- BG
- Bulgaria
- Prior art keywords
- weight
- trans
- tet
- preparation
- tetramethrin
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 title 1
- 239000013543 active substance Substances 0.000 claims abstract description 18
- 238000002360 preparation method Methods 0.000 claims abstract description 18
- 239000002728 pyrethroid Substances 0.000 claims abstract description 13
- FIPWRIJSWJWJAI-UHFFFAOYSA-N Butyl carbitol 6-propylpiperonyl ether Chemical compound C1=C(CCC)C(COCCOCCOCCCC)=CC2=C1OCO2 FIPWRIJSWJWJAI-UHFFFAOYSA-N 0.000 claims abstract description 12
- 229960005235 piperonyl butoxide Drugs 0.000 claims abstract description 12
- 241000238421 Arthropoda Species 0.000 claims abstract description 9
- 230000002195 synergetic effect Effects 0.000 claims abstract description 6
- 239000000654 additive Substances 0.000 claims abstract description 4
- 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 abstract description 3
- -1 2,2-dichlorovinyl Chemical group 0.000 claims description 8
- 210000004369 blood Anatomy 0.000 claims description 3
- 102100035861 Cytosolic 5'-nucleotidase 1A Human genes 0.000 claims 1
- 101000802744 Homo sapiens Cytosolic 5'-nucleotidase 1A Proteins 0.000 claims 1
- CXBMCYHAMVGWJQ-CABCVRRESA-N (1,3-dioxo-4,5,6,7-tetrahydroisoindol-2-yl)methyl (1r,3r)-2,2-dimethyl-3-(2-methylprop-1-enyl)cyclopropane-1-carboxylate Chemical compound CC1(C)[C@H](C=C(C)C)[C@H]1C(=O)OCN1C(=O)C(CCCC2)=C2C1=O CXBMCYHAMVGWJQ-CABCVRRESA-N 0.000 abstract description 14
- 241001465754 Metazoa Species 0.000 abstract description 6
- 231100000053 low toxicity Toxicity 0.000 abstract description 2
- 239000000203 mixture Substances 0.000 description 23
- 241000255925 Diptera Species 0.000 description 15
- 239000000243 solution Substances 0.000 description 14
- 230000000694 effects Effects 0.000 description 12
- 229960005199 tetramethrin Drugs 0.000 description 12
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 11
- 241000238631 Hexapoda Species 0.000 description 10
- 239000004615 ingredient Substances 0.000 description 10
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 9
- 241000607479 Yersinia pestis Species 0.000 description 9
- 239000008096 xylene Substances 0.000 description 9
- 239000000839 emulsion Substances 0.000 description 8
- 239000000126 substance Substances 0.000 description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 6
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 6
- 239000000843 powder Substances 0.000 description 6
- 238000000034 method Methods 0.000 description 5
- 239000002736 nonionic surfactant Substances 0.000 description 5
- 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 description 5
- 229960000490 permethrin Drugs 0.000 description 5
- 239000002904 solvent Substances 0.000 description 5
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 4
- 238000009472 formulation Methods 0.000 description 4
- 241000254173 Coleoptera Species 0.000 description 3
- 101710097943 Viral-enhancing factor Proteins 0.000 description 3
- 239000003945 anionic surfactant Substances 0.000 description 3
- 239000012141 concentrate Substances 0.000 description 3
- KAATUXNTWXVJKI-UHFFFAOYSA-N cypermethrin Chemical class 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 description 3
- 230000006378 damage Effects 0.000 description 3
- 238000010790 dilution Methods 0.000 description 3
- 239000012895 dilution Substances 0.000 description 3
- 235000021186 dishes Nutrition 0.000 description 3
- 229960000878 docusate sodium Drugs 0.000 description 3
- APSBXTVYXVQYAB-UHFFFAOYSA-M sodium docusate Chemical compound [Na+].CCCCC(CC)COC(=O)CC(S([O-])(=O)=O)C(=O)OCC(CC)CCCC APSBXTVYXVQYAB-UHFFFAOYSA-M 0.000 description 3
- 239000007921 spray Substances 0.000 description 3
- 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 2
- JKTAIYGNOFSMCE-UHFFFAOYSA-N 2,3-di(nonyl)phenol Chemical compound CCCCCCCCCC1=CC=CC(O)=C1CCCCCCCCC JKTAIYGNOFSMCE-UHFFFAOYSA-N 0.000 description 2
- 241000238876 Acari Species 0.000 description 2
- 241000238657 Blattella germanica Species 0.000 description 2
- 239000005909 Kieselgur Substances 0.000 description 2
- 241000257159 Musca domestica Species 0.000 description 2
- 241000257226 Muscidae Species 0.000 description 2
- 230000000996 additive effect Effects 0.000 description 2
- 238000004458 analytical method Methods 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- 239000008280 blood Substances 0.000 description 2
- 239000001569 carbon dioxide Substances 0.000 description 2
- 229910002092 carbon dioxide Inorganic materials 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 229960002483 decamethrin Drugs 0.000 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 description 2
- 239000002270 dispersing agent Substances 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 229910052500 inorganic mineral Inorganic materials 0.000 description 2
- 230000003993 interaction Effects 0.000 description 2
- 239000002480 mineral oil Substances 0.000 description 2
- 210000005036 nerve Anatomy 0.000 description 2
- SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical compound CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 2
- 239000004033 plastic Substances 0.000 description 2
- 159000000000 sodium salts Chemical class 0.000 description 2
- 239000002689 soil Substances 0.000 description 2
- 230000000699 topical effect Effects 0.000 description 2
- 235000015112 vegetable and seed oil Nutrition 0.000 description 2
- 239000008158 vegetable oil Substances 0.000 description 2
- 238000009736 wetting Methods 0.000 description 2
- KAATUXNTWXVJKI-NSHGMRRFSA-N (1R)-cis-(alphaS)-cypermethrin Chemical compound CC1(C)[C@@H](C=C(Cl)Cl)[C@H]1C(=O)O[C@H](C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 KAATUXNTWXVJKI-NSHGMRRFSA-N 0.000 description 1
- RLLPVAHGXHCWKJ-HKUYNNGSSA-N (3-phenoxyphenyl)methyl (1r,3r)-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-HKUYNNGSSA-N 0.000 description 1
- OHAMOQALFCXZBV-UHFFFAOYSA-N 2,2-dichloroethenyl 2,2-dimethylcyclopropane-1-carboxylate Chemical compound CC1(C)CC1C(=O)OC=C(Cl)Cl OHAMOQALFCXZBV-UHFFFAOYSA-N 0.000 description 1
- IEORSVTYLWZQJQ-UHFFFAOYSA-N 2-(2-nonylphenoxy)ethanol Chemical compound CCCCCCCCCC1=CC=CC=C1OCCO IEORSVTYLWZQJQ-UHFFFAOYSA-N 0.000 description 1
- ZNQVEEAIQZEUHB-UHFFFAOYSA-N 2-ethoxyethanol Chemical compound CCOCCO ZNQVEEAIQZEUHB-UHFFFAOYSA-N 0.000 description 1
- 241000238702 Acariformes Species 0.000 description 1
- 206010063409 Acarodermatitis Diseases 0.000 description 1
- 208000000230 African Trypanosomiasis Diseases 0.000 description 1
- 206010002091 Anaesthesia Diseases 0.000 description 1
- 241001035438 Anthracus Species 0.000 description 1
- 206010004194 Bed bug infestation Diseases 0.000 description 1
- 241001674044 Blattodea Species 0.000 description 1
- 241001325378 Bruchus Species 0.000 description 1
- OYPRJOBELJOOCE-BKFZFHPZSA-N Calcium-45 Chemical class [45Ca] OYPRJOBELJOOCE-BKFZFHPZSA-N 0.000 description 1
- 241001414836 Cimex Species 0.000 description 1
- 241001414835 Cimicidae Species 0.000 description 1
- 208000035473 Communicable disease Diseases 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- 241000268912 Damalinia Species 0.000 description 1
- 239000005892 Deltamethrin Substances 0.000 description 1
- 241001641895 Dermestes Species 0.000 description 1
- 241000258937 Hemiptera Species 0.000 description 1
- 241000257303 Hymenoptera Species 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
- 241000238681 Ixodes Species 0.000 description 1
- 241000255777 Lepidoptera Species 0.000 description 1
- 241001332052 Longipalpa Species 0.000 description 1
- 241000570861 Mandragora autumnalis Species 0.000 description 1
- 241000145847 Moria Species 0.000 description 1
- 241000041821 Necrobia Species 0.000 description 1
- IGFHQQFPSIBGKE-UHFFFAOYSA-N Nonylphenol Natural products CCCCCCCCCC1=CC=C(O)C=C1 IGFHQQFPSIBGKE-UHFFFAOYSA-N 0.000 description 1
- 239000005662 Paraffin oil Substances 0.000 description 1
- 241000517325 Pediculus Species 0.000 description 1
- 241001674048 Phthiraptera Species 0.000 description 1
- 206010035148 Plague Diseases 0.000 description 1
- 241000985694 Polypodiopsida Species 0.000 description 1
- 241000447727 Scabies Species 0.000 description 1
- 241000134399 Simulium sp. Species 0.000 description 1
- 241001177162 Stegobium Species 0.000 description 1
- 241001494115 Stomoxys calcitrans Species 0.000 description 1
- 241000282887 Suidae Species 0.000 description 1
- 235000019486 Sunflower oil Nutrition 0.000 description 1
- 241000254105 Tenebrio Species 0.000 description 1
- 241000254086 Tribolium <beetle> Species 0.000 description 1
- 241000254112 Tribolium confusum Species 0.000 description 1
- 208000003152 Yellow Fever Diseases 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 125000002877 alkyl aryl group Chemical group 0.000 description 1
- 150000008055 alkyl aryl sulfonates Chemical class 0.000 description 1
- 230000002009 allergenic effect Effects 0.000 description 1
- AVKUERGKIZMTKX-NJBDSQKTSA-N ampicillin Chemical compound C1([C@@H](N)C(=O)N[C@H]2[C@H]3SC([C@@H](N3C2=O)C(O)=O)(C)C)=CC=CC=C1 AVKUERGKIZMTKX-NJBDSQKTSA-N 0.000 description 1
- 230000037005 anaesthesia Effects 0.000 description 1
- 230000003042 antagnostic effect Effects 0.000 description 1
- 230000008485 antagonism Effects 0.000 description 1
- 239000003849 aromatic solvent Substances 0.000 description 1
- 239000011324 bead Substances 0.000 description 1
- 235000008429 bread Nutrition 0.000 description 1
- OOCMUZJPDXYRFD-UHFFFAOYSA-L calcium;2-dodecylbenzenesulfonate Chemical compound [Ca+2].CCCCCCCCCCCCC1=CC=CC=C1S([O-])(=O)=O.CCCCCCCCCCCCC1=CC=CC=C1S([O-])(=O)=O OOCMUZJPDXYRFD-UHFFFAOYSA-L 0.000 description 1
- 238000004364 calculation method Methods 0.000 description 1
- 238000009924 canning Methods 0.000 description 1
- 235000013339 cereals Nutrition 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- YMGUBTXCNDTFJI-UHFFFAOYSA-M cyclopropanecarboxylate Chemical compound [O-]C(=O)C1CC1 YMGUBTXCNDTFJI-UHFFFAOYSA-M 0.000 description 1
- 230000001066 destructive effect Effects 0.000 description 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 1
- 208000035475 disorder Diseases 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000002500 effect on skin Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 235000013312 flour Nutrition 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 238000007710 freezing Methods 0.000 description 1
- 230000008014 freezing Effects 0.000 description 1
- 229910052732 germanium Inorganic materials 0.000 description 1
- GNPVGFCGXDBREM-UHFFFAOYSA-N germanium atom Chemical compound [Ge] GNPVGFCGXDBREM-UHFFFAOYSA-N 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- 208000029080 human African trypanosomiasis Diseases 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 239000002085 irritant Substances 0.000 description 1
- 231100000021 irritant Toxicity 0.000 description 1
- 229940057995 liquid paraffin Drugs 0.000 description 1
- 244000144972 livestock Species 0.000 description 1
- 238000011068 loading method Methods 0.000 description 1
- 201000004792 malaria Diseases 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- PSZYNBSKGUBXEH-UHFFFAOYSA-N naphthalene-1-sulfonic acid Chemical compound C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-N 0.000 description 1
- 239000006199 nebulizer Substances 0.000 description 1
- 229920000847 nonoxynol Polymers 0.000 description 1
- 231100000252 nontoxic Toxicity 0.000 description 1
- 230000003000 nontoxic effect Effects 0.000 description 1
- 125000001400 nonyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 244000045947 parasite Species 0.000 description 1
- 239000000546 pharmaceutical excipient Substances 0.000 description 1
- 239000002574 poison Substances 0.000 description 1
- 231100000614 poison Toxicity 0.000 description 1
- 210000003689 pubic bone Anatomy 0.000 description 1
- 208000005687 scabies Diseases 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 238000003307 slaughter Methods 0.000 description 1
- 201000002612 sleeping sickness Diseases 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 235000014347 soups Nutrition 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000002600 sunflower oil Substances 0.000 description 1
- 208000024891 symptom Diseases 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- AGGKEGLBGGJEBZ-UHFFFAOYSA-N tetramethylenedisulfotetramine Chemical compound C1N(S2(=O)=O)CN3S(=O)(=O)N1CN2C3 AGGKEGLBGGJEBZ-UHFFFAOYSA-N 0.000 description 1
- 239000003643 water by type Substances 0.000 description 1
- 230000003442 weekly effect Effects 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
- A01N53/00—Biocides, pest repellants or attractants, or plant growth regulators containing cyclopropane carboxylic acids or derivatives thereof
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)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| HU88540A HU198830B (en) | 1988-02-05 | 1988-02-05 | Arthropodicides comprising cypermethrin trans-isomers and tetramethrin |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| BG60284B2 true BG60284B2 (bg) | 1994-04-25 |
Family
ID=10950075
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| BG087126A BG60284B2 (bg) | 1988-02-05 | 1989-02-03 | Артроподен препарат |
Country Status (29)
| Country | Link |
|---|---|
| US (1) | US4950682A (fr) |
| EP (1) | EP0327467B1 (fr) |
| JP (1) | JPH0768093B2 (fr) |
| KR (1) | KR950002852B1 (fr) |
| CN (1) | CN1028345C (fr) |
| AU (1) | AU627445B2 (fr) |
| BG (1) | BG60284B2 (fr) |
| CA (1) | CA1317218C (fr) |
| CZ (1) | CZ287305B6 (fr) |
| DD (1) | DD278713A5 (fr) |
| DE (1) | DE68911160T2 (fr) |
| DK (1) | DK51689A (fr) |
| EG (1) | EG18772A (fr) |
| ES (1) | ES2012674A6 (fr) |
| FI (1) | FI97017C (fr) |
| GR (1) | GR1000584B (fr) |
| HK (1) | HK1003968A1 (fr) |
| HU (1) | HU198830B (fr) |
| IE (1) | IE64475B1 (fr) |
| IL (1) | IL89180A (fr) |
| NO (1) | NO174134C (fr) |
| NZ (1) | NZ227887A (fr) |
| PL (1) | PL154475B1 (fr) |
| PT (1) | PT89616B (fr) |
| RO (1) | RO104069B1 (fr) |
| RU (1) | RU2069058C1 (fr) |
| SK (1) | SK279882B6 (fr) |
| UA (1) | UA26842C2 (fr) |
| ZA (1) | ZA89796B (fr) |
Families Citing this family (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB8912188D0 (en) * | 1989-05-26 | 1989-07-12 | Wellcome Found | Pesticidal compositions |
| IT1247917B (it) * | 1991-05-10 | 1995-01-05 | Endura Spa | Composizioni insetticide contenenti miscele ternarie di derivati del metilendiossibenzene e procedimento per la loro preparazione |
| AU666399B2 (en) * | 1992-09-21 | 1996-02-08 | Virbac (Australia) Pty Limited | Pesticidal compositions |
| FR2729541B1 (fr) * | 1995-01-20 | 2000-12-01 | Jean Claude Attali | Microemulsion aqueuse insecticide et parasiticide , son procede de fabrication et d'utilisation |
| ES2170243T3 (es) * | 1996-06-11 | 2002-08-01 | Attavet | Composicion insecticida y parasiticida acuosa, su procedimiento de fabricacion y de utilizacion. |
| US5906983A (en) * | 1997-08-20 | 1999-05-25 | The Clorox Company | High fructose containing insecticide compositions and methods of using the same |
| US6117854A (en) * | 1997-08-20 | 2000-09-12 | The Clorox Company | Enhanced performance insecticide compositions containing plant derived oil carriers and methods of using the same |
| TW402485B (en) * | 1998-05-26 | 2000-08-21 | Sumitomo Chemical Co | Pyrethroid compound and composition for controlling pest containing the same as an active ingredient |
| AUPP858299A0 (en) * | 1999-02-08 | 1999-03-04 | Virbac (Australia) Pty Limited | Pesticidal compositions |
| WO2001036192A1 (fr) * | 1999-11-18 | 2001-05-25 | Ming Zhang | Profil en acier-plastique et son procede de fabrication |
| GB0209749D0 (en) * | 2002-04-29 | 2002-06-05 | Rothamsted Ex Res Station | Compositions and methods |
| US6958146B2 (en) * | 2003-05-28 | 2005-10-25 | Bug Buster Ltd. | Compounds to affect insect behavior and to enhance insecticides |
| US7867479B2 (en) * | 2003-11-14 | 2011-01-11 | Bug Buster, Ltd. | Compounds to affect insect behavior and/or bird behavior |
| JP5066915B2 (ja) * | 2006-04-03 | 2012-11-07 | 住友化学株式会社 | １，３−ベンズジオキソール化合物とその用途 |
| CN106857635A (zh) * | 2016-12-31 | 2017-06-20 | 新昌县云河虫害防治技术开发有限公司 | 家用杀虫剂及其用途 |
Family Cites Families (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3067091A (en) * | 1958-06-03 | 1962-12-04 | Phillips Petroleum Co | Insect combatting |
| US3308015A (en) * | 1965-10-21 | 1967-03-07 | Richardson Merrell Inc | Synergistic insecticidal compositions |
| JPS5851921B2 (ja) * | 1973-10-15 | 1983-11-19 | 住友化学工業株式会社 | ソツコウセイサツチユウ サツダニソセイブツ |
| FR2341307A1 (fr) * | 1976-02-19 | 1977-09-16 | Roussel Uclaf | Pyrethrinoides a titre de medicaments et compositions pharmaceutiques les renfermant |
| DE2704066A1 (de) * | 1977-02-01 | 1978-08-03 | Neudorff & Co Chem Fab W | Insektizidgemisch |
| NZ190600A (en) * | 1978-05-30 | 1982-03-09 | Wellcome Found | Arthropodicidal compositions containing cyclopropane-carboxylic acid ester derivatives |
| JPS5527104A (en) * | 1978-07-19 | 1980-02-27 | Sumitomo Chem Co Ltd | Pesticidal composition |
| FR2500265A1 (fr) * | 1981-02-20 | 1982-08-27 | Roussel Uclaf | Compositions pesticides contenant un melange synergique de 1r, cis 2,2-dimethyl 3(2,2-dihalovinyl) cyclopropane-1-carboxylate de (s) a-cyano 3-phenoxybenzyle et d'autres composes pyrethrinoides |
| EP0064803B1 (fr) * | 1981-04-27 | 1985-11-21 | Imperial Chemical Industries Plc | Compositions insecticides |
| HU190818B (en) * | 1982-11-09 | 1986-11-28 | Chinoin Gyogyszer Es Vegyeszeti Termekek Gyara Rt,Hu | Process for producing complexes of piperonyl-butoxide-cyclodextrin |
| CA1275108A (fr) * | 1985-01-16 | 1990-10-09 | Laszlo Pap | Composition insecticide renfermant plus d'un agent actif |
-
1988
- 1988-02-05 HU HU88540A patent/HU198830B/hu not_active IP Right Cessation
-
1989
- 1989-02-01 ZA ZA89796A patent/ZA89796B/xx unknown
- 1989-02-02 IE IE33089A patent/IE64475B1/en not_active IP Right Cessation
- 1989-02-03 DK DK051689A patent/DK51689A/da not_active Application Discontinuation
- 1989-02-03 NO NO890453A patent/NO174134C/no not_active IP Right Cessation
- 1989-02-03 SK SK760-89A patent/SK279882B6/sk unknown
- 1989-02-03 CZ CZ1989760A patent/CZ287305B6/cs not_active IP Right Cessation
- 1989-02-03 EP EP89400317A patent/EP0327467B1/fr not_active Expired - Lifetime
- 1989-02-03 RU SU894613484A patent/RU2069058C1/ru not_active IP Right Cessation
- 1989-02-03 PT PT89616A patent/PT89616B/pt not_active IP Right Cessation
- 1989-02-03 DE DE68911160T patent/DE68911160T2/de not_active Expired - Fee Related
- 1989-02-03 DD DD89325509A patent/DD278713A5/de not_active IP Right Cessation
- 1989-02-03 RO RO138068A patent/RO104069B1/ro unknown
- 1989-02-03 FI FI890527A patent/FI97017C/fi not_active IP Right Cessation
- 1989-02-03 UA UA4613484A patent/UA26842C2/uk unknown
- 1989-02-03 BG BG087126A patent/BG60284B2/bg unknown
- 1989-02-05 IL IL8918089A patent/IL89180A/en not_active IP Right Cessation
- 1989-02-05 EG EG57/89A patent/EG18772A/xx active
- 1989-02-05 CN CN89102120A patent/CN1028345C/zh not_active Expired - Fee Related
- 1989-02-06 US US07/307,395 patent/US4950682A/en not_active Expired - Lifetime
- 1989-02-06 PL PL1989277599A patent/PL154475B1/pl unknown
- 1989-02-06 AU AU29650/89A patent/AU627445B2/en not_active Ceased
- 1989-02-06 ES ES8900790A patent/ES2012674A6/es not_active Expired - Lifetime
- 1989-02-06 JP JP1027340A patent/JPH0768093B2/ja not_active Expired - Fee Related
- 1989-02-06 CA CA000590182A patent/CA1317218C/fr not_active Expired - Fee Related
- 1989-02-06 GR GR890100068A patent/GR1000584B/el not_active IP Right Cessation
- 1989-02-07 NZ NZ227887A patent/NZ227887A/en unknown
- 1989-02-08 KR KR1019890001428A patent/KR950002852B1/ko not_active IP Right Cessation
-
1998
- 1998-04-16 HK HK98103153A patent/HK1003968A1/xx not_active IP Right Cessation
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