NL8400893A - Organotinverbinding, werkwijze voor het bereiden daarvan, deze verbinding bevattende insecticide- en acaricidepreparaten en methode voor het bestrijden van fytofage insecten en acariden. - Google Patents
Organotinverbinding, werkwijze voor het bereiden daarvan, deze verbinding bevattende insecticide- en acaricidepreparaten en methode voor het bestrijden van fytofage insecten en acariden. Download PDFInfo
- Publication number
- NL8400893A NL8400893A NL8400893A NL8400893A NL8400893A NL 8400893 A NL8400893 A NL 8400893A NL 8400893 A NL8400893 A NL 8400893A NL 8400893 A NL8400893 A NL 8400893A NL 8400893 A NL8400893 A NL 8400893A
- Authority
- NL
- Netherlands
- Prior art keywords
- compound
- derivative
- preparation
- active ingredient
- acarides
- Prior art date
Links
- 238000002360 preparation method Methods 0.000 title claims description 31
- 150000001875 compounds Chemical class 0.000 title claims description 18
- 238000000034 method Methods 0.000 title claims description 13
- 230000000895 acaricidal effect Effects 0.000 title claims description 8
- 241000238631 Hexapoda Species 0.000 title claims description 7
- 239000000642 acaricide Chemical class 0.000 title claims description 5
- 239000002917 insecticide Chemical class 0.000 title claims description 4
- 239000004480 active ingredient Substances 0.000 claims description 26
- 239000004495 emulsifiable concentrate Substances 0.000 claims description 14
- WCMMILVIRZAPLE-UHFFFAOYSA-M cyhexatin Chemical compound C1CCCCC1[Sn](C1CCCCC1)(O)C1CCCCC1 WCMMILVIRZAPLE-UHFFFAOYSA-M 0.000 claims description 12
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 12
- YLTNMVLVPUHWLQ-UHFFFAOYSA-M tricyclohexylstannyl benzoate Chemical group C=1C=CC=CC=1C(=O)O[Sn](C1CCCCC1)(C1CCCCC1)C1CCCCC1 YLTNMVLVPUHWLQ-UHFFFAOYSA-M 0.000 claims description 8
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 claims description 7
- 230000000749 insecticidal effect Effects 0.000 claims description 5
- 239000005711 Benzoic acid Substances 0.000 claims description 3
- 235000010233 benzoic acid Nutrition 0.000 claims description 3
- 238000006243 chemical reaction Methods 0.000 claims description 3
- HXJNZPXGMGELDP-UHFFFAOYSA-J tin(4+);tetrabenzoate Chemical compound [Sn+4].[O-]C(=O)C1=CC=CC=C1.[O-]C(=O)C1=CC=CC=C1.[O-]C(=O)C1=CC=CC=C1.[O-]C(=O)C1=CC=CC=C1 HXJNZPXGMGELDP-UHFFFAOYSA-J 0.000 claims 1
- RNVJQUPAEIQUTC-UHFFFAOYSA-N tricyclohexyltin Chemical class C1CCCCC1[Sn](C1CCCCC1)C1CCCCC1 RNVJQUPAEIQUTC-UHFFFAOYSA-N 0.000 claims 1
- 239000000203 mixture Substances 0.000 description 16
- 239000000843 powder Substances 0.000 description 12
- 241000196324 Embryophyta Species 0.000 description 11
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 11
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 9
- 239000004563 wettable powder Substances 0.000 description 9
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 8
- -1 penetrants Substances 0.000 description 8
- 239000000243 solution Substances 0.000 description 7
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 6
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 6
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
- 239000000839 emulsion Substances 0.000 description 6
- 239000007787 solid Substances 0.000 description 6
- 239000000654 additive Substances 0.000 description 5
- 239000003795 chemical substances by application Substances 0.000 description 5
- 230000000694 effects Effects 0.000 description 5
- 239000007788 liquid Substances 0.000 description 5
- 150000003839 salts Chemical class 0.000 description 5
- 239000000377 silicon dioxide Substances 0.000 description 5
- 239000003381 stabilizer Substances 0.000 description 5
- 239000004094 surface-active agent Substances 0.000 description 5
- 239000005995 Aluminium silicate Substances 0.000 description 4
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 4
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 4
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 4
- 235000011941 Tilia x europaea Nutrition 0.000 description 4
- 239000000853 adhesive Substances 0.000 description 4
- 230000001070 adhesive effect Effects 0.000 description 4
- 235000012211 aluminium silicate Nutrition 0.000 description 4
- 235000019993 champagne Nutrition 0.000 description 4
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 4
- 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 4
- 239000004571 lime Substances 0.000 description 4
- 235000012239 silicon dioxide Nutrition 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- 239000008096 xylene Substances 0.000 description 4
- WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 description 3
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 3
- 230000000996 additive effect Effects 0.000 description 3
- 239000000969 carrier Substances 0.000 description 3
- 238000001035 drying Methods 0.000 description 3
- 238000010410 dusting Methods 0.000 description 3
- 239000003995 emulsifying agent Substances 0.000 description 3
- PSZYNBSKGUBXEH-UHFFFAOYSA-N naphthalene-1-sulfonic acid Chemical class C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-N 0.000 description 3
- 239000002244 precipitate Substances 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- KWOLFJPFCHCOCG-UHFFFAOYSA-N Acetophenone Chemical compound CC(=O)C1=CC=CC=C1 KWOLFJPFCHCOCG-UHFFFAOYSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- 239000004354 Hydroxyethyl cellulose Substances 0.000 description 2
- 229920000663 Hydroxyethyl cellulose Polymers 0.000 description 2
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 2
- 244000046052 Phaseolus vulgaris Species 0.000 description 2
- 239000003905 agrochemical Substances 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- 229910052783 alkali metal Inorganic materials 0.000 description 2
- 239000010692 aromatic oil Substances 0.000 description 2
- 239000003849 aromatic solvent Substances 0.000 description 2
- SRSXLGNVWSONIS-UHFFFAOYSA-N benzenesulfonic acid Chemical class OS(=O)(=O)C1=CC=CC=C1 SRSXLGNVWSONIS-UHFFFAOYSA-N 0.000 description 2
- 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 2
- 239000004359 castor oil Substances 0.000 description 2
- 235000019438 castor oil Nutrition 0.000 description 2
- 239000012141 concentrate Substances 0.000 description 2
- 239000007859 condensation product Substances 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 238000005260 corrosion Methods 0.000 description 2
- 230000007797 corrosion Effects 0.000 description 2
- 238000007865 diluting Methods 0.000 description 2
- 239000002270 dispersing agent Substances 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- 229940071161 dodecylbenzenesulfonate Drugs 0.000 description 2
- 239000000975 dye Substances 0.000 description 2
- 150000002191 fatty alcohols Chemical class 0.000 description 2
- 239000003337 fertilizer Substances 0.000 description 2
- 239000000706 filtrate Substances 0.000 description 2
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 2
- 239000008187 granular material Substances 0.000 description 2
- 235000019447 hydroxyethyl cellulose Nutrition 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- 239000003112 inhibitor Substances 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 2
- 229910052753 mercury Inorganic materials 0.000 description 2
- 239000003595 mist Substances 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- 239000010690 paraffinic oil Substances 0.000 description 2
- 150000002989 phenols Chemical class 0.000 description 2
- KZOJQMWTKJDSQJ-UHFFFAOYSA-M sodium;2,3-dibutylnaphthalene-1-sulfonate Chemical compound [Na+].C1=CC=C2C(S([O-])(=O)=O)=C(CCCC)C(CCCC)=CC2=C1 KZOJQMWTKJDSQJ-UHFFFAOYSA-M 0.000 description 2
- 239000002689 soil Substances 0.000 description 2
- 238000005507 spraying Methods 0.000 description 2
- 239000000725 suspension Substances 0.000 description 2
- 239000000454 talc Substances 0.000 description 2
- 229910052623 talc Inorganic materials 0.000 description 2
- 239000013008 thixotropic agent Substances 0.000 description 2
- 239000000080 wetting agent Substances 0.000 description 2
- ABJSOROVZZKJGI-OCYUSGCXSA-N (1r,2r,4r)-2-(4-bromophenyl)-n-[(4-chlorophenyl)-(2-fluoropyridin-4-yl)methyl]-4-morpholin-4-ylcyclohexane-1-carboxamide Chemical compound C1=NC(F)=CC(C(NC(=O)[C@H]2[C@@H](C[C@@H](CC2)N2CCOCC2)C=2C=CC(Br)=CC=2)C=2C=CC(Cl)=CC=2)=C1 ABJSOROVZZKJGI-OCYUSGCXSA-N 0.000 description 1
- HSINOMROUCMIEA-FGVHQWLLSA-N (2s,4r)-4-[(3r,5s,6r,7r,8s,9s,10s,13r,14s,17r)-6-ethyl-3,7-dihydroxy-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1h-cyclopenta[a]phenanthren-17-yl]-2-methylpentanoic acid Chemical class C([C@@]12C)C[C@@H](O)C[C@H]1[C@@H](CC)[C@@H](O)[C@@H]1[C@@H]2CC[C@]2(C)[C@@H]([C@H](C)C[C@H](C)C(O)=O)CC[C@H]21 HSINOMROUCMIEA-FGVHQWLLSA-N 0.000 description 1
- 238000005160 1H NMR spectroscopy Methods 0.000 description 1
- TVFWYUWNQVRQRG-UHFFFAOYSA-N 2,3,4-tris(2-phenylethenyl)phenol Chemical compound C=1C=CC=CC=1C=CC1=C(C=CC=2C=CC=CC=2)C(O)=CC=C1C=CC1=CC=CC=C1 TVFWYUWNQVRQRG-UHFFFAOYSA-N 0.000 description 1
- FOGYNLXERPKEGN-UHFFFAOYSA-N 3-(2-hydroxy-3-methoxyphenyl)-2-[2-methoxy-4-(3-sulfopropyl)phenoxy]propane-1-sulfonic acid Chemical class COC1=CC=CC(CC(CS(O)(=O)=O)OC=2C(=CC(CCCS(O)(=O)=O)=CC=2)OC)=C1O FOGYNLXERPKEGN-UHFFFAOYSA-N 0.000 description 1
- 235000011293 Brassica napus Nutrition 0.000 description 1
- 240000008100 Brassica rapa Species 0.000 description 1
- 235000000540 Brassica rapa subsp rapa Nutrition 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 239000005946 Cypermethrin Substances 0.000 description 1
- 240000005323 Hoya carnosa 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
- 239000005909 Kieselgur Substances 0.000 description 1
- 235000010654 Melissa officinalis Nutrition 0.000 description 1
- IGFHQQFPSIBGKE-UHFFFAOYSA-N Nonylphenol Natural products CCCCCCCCCC1=CC=C(O)C=C1 IGFHQQFPSIBGKE-UHFFFAOYSA-N 0.000 description 1
- 231100000674 Phytotoxicity Toxicity 0.000 description 1
- 241000500439 Plutella Species 0.000 description 1
- 229920002125 Sokalan® Polymers 0.000 description 1
- 241001454293 Tetranychus urticae Species 0.000 description 1
- 241000607479 Yersinia pestis Species 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000000443 aerosol Substances 0.000 description 1
- 238000005054 agglomeration Methods 0.000 description 1
- 230000002776 aggregation Effects 0.000 description 1
- 150000008055 alkyl aryl sulfonates Chemical class 0.000 description 1
- 125000005907 alkyl ester group Chemical group 0.000 description 1
- DNEHKUCSURWDGO-UHFFFAOYSA-N aluminum sodium Chemical compound [Na].[Al] DNEHKUCSURWDGO-UHFFFAOYSA-N 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 239000002518 antifoaming agent Substances 0.000 description 1
- 239000007900 aqueous suspension Substances 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 238000010533 azeotropic distillation Methods 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229920005551 calcium lignosulfonate Polymers 0.000 description 1
- RYAGRZNBULDMBW-UHFFFAOYSA-L calcium;3-(2-hydroxy-3-methoxyphenyl)-2-[2-methoxy-4-(3-sulfonatopropyl)phenoxy]propane-1-sulfonate Chemical compound [Ca+2].COC1=CC=CC(CC(CS([O-])(=O)=O)OC=2C(=CC(CCCS([O-])(=O)=O)=CC=2)OC)=C1O RYAGRZNBULDMBW-UHFFFAOYSA-L 0.000 description 1
- 150000008280 chlorinated hydrocarbons Chemical class 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 239000000084 colloidal system Substances 0.000 description 1
- 230000000295 complement effect Effects 0.000 description 1
- 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 description 1
- 229960005424 cypermethrin Drugs 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 230000001804 emulsifying effect Effects 0.000 description 1
- 230000032050 esterification Effects 0.000 description 1
- 238000005886 esterification reaction Methods 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 238000007710 freezing Methods 0.000 description 1
- 230000008014 freezing Effects 0.000 description 1
- 230000000855 fungicidal effect Effects 0.000 description 1
- 239000000417 fungicide Substances 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- 239000003906 humectant Substances 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 238000005470 impregnation Methods 0.000 description 1
- 229910017053 inorganic salt Inorganic materials 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 231100000636 lethal dose Toxicity 0.000 description 1
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 1
- 235000019341 magnesium sulphate Nutrition 0.000 description 1
- 239000008268 mayonnaise Substances 0.000 description 1
- 235000010746 mayonnaise Nutrition 0.000 description 1
- SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical compound CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 239000000575 pesticide Substances 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 150000003014 phosphoric acid esters Chemical class 0.000 description 1
- 230000008635 plant growth Effects 0.000 description 1
- 239000005648 plant growth regulator Substances 0.000 description 1
- 239000004584 polyacrylic acid Substances 0.000 description 1
- 239000010695 polyglycol Substances 0.000 description 1
- 229920000151 polyglycol Polymers 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- ARENMZZMCSLORU-UHFFFAOYSA-N propan-2-yl naphthalene-1-sulfonate Chemical compound C1=CC=C2C(S(=O)(=O)OC(C)C)=CC=CC2=C1 ARENMZZMCSLORU-UHFFFAOYSA-N 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000003352 sequestering agent Substances 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- SRAWNDFHGTVUNZ-UHFFFAOYSA-M sodium;3,6-dibutylnaphthalene-1-sulfonate Chemical compound [Na+].[O-]S(=O)(=O)C1=CC(CCCC)=CC2=CC(CCCC)=CC=C21 SRAWNDFHGTVUNZ-UHFFFAOYSA-M 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000004546 suspension concentrate Substances 0.000 description 1
- 238000013268 sustained release Methods 0.000 description 1
- 239000012730 sustained-release form Substances 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 150000003606 tin compounds Chemical class 0.000 description 1
- AMFGTOFWMRQMEM-UHFFFAOYSA-N triazophos Chemical compound N1=C(OP(=S)(OCC)OCC)N=CN1C1=CC=CC=C1 AMFGTOFWMRQMEM-UHFFFAOYSA-N 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 238000009423 ventilation Methods 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 238000009736 wetting Methods 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
-
- 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
- A01N55/00—Biocides, pest repellants or attractants, or plant growth regulators, containing organic compounds containing elements other than carbon, hydrogen, halogen, oxygen, nitrogen and sulfur
- A01N55/02—Biocides, pest repellants or attractants, or plant growth regulators, containing organic compounds containing elements other than carbon, hydrogen, halogen, oxygen, nitrogen and sulfur containing metal atoms
- A01N55/04—Tin
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/22—Tin compounds
- C07F7/2224—Compounds having one or more tin-oxygen linkages
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Organic Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- Pest Control & Pesticides (AREA)
- Zoology (AREA)
- Wood Science & Technology (AREA)
- Environmental Sciences (AREA)
- Plant Pathology (AREA)
- Agronomy & Crop Science (AREA)
- Toxicology (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR8304884 | 1983-03-22 | ||
FR8304884A FR2543142B1 (fr) | 1983-03-22 | 1983-03-22 | Ester de l'hydroxyde de tricyclohexyletain acaricide |
Publications (1)
Publication Number | Publication Date |
---|---|
NL8400893A true NL8400893A (nl) | 1984-10-16 |
Family
ID=9287208
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
NL8400893A NL8400893A (nl) | 1983-03-22 | 1984-03-21 | Organotinverbinding, werkwijze voor het bereiden daarvan, deze verbinding bevattende insecticide- en acaricidepreparaten en methode voor het bestrijden van fytofage insecten en acariden. |
Country Status (24)
Country | Link |
---|---|
US (1) | US4602945A (fr) |
JP (1) | JPS59176296A (fr) |
KR (1) | KR840007808A (fr) |
AU (1) | AU2591984A (fr) |
BE (1) | BE899225A (fr) |
BR (1) | BR8401318A (fr) |
CA (1) | CA1231716A (fr) |
CH (1) | CH660365A5 (fr) |
DE (1) | DE3410064A1 (fr) |
DK (1) | DK136284D0 (fr) |
ES (1) | ES530812A0 (fr) |
FR (1) | FR2543142B1 (fr) |
GB (1) | GB2136811B (fr) |
GR (1) | GR81825B (fr) |
HU (1) | HUT33961A (fr) |
IL (1) | IL71165A0 (fr) |
IT (1) | IT1177597B (fr) |
LU (1) | LU85259A1 (fr) |
NL (1) | NL8400893A (fr) |
NZ (1) | NZ207559A (fr) |
OA (1) | OA07683A (fr) |
PH (1) | PH20025A (fr) |
PT (1) | PT78291B (fr) |
ZA (1) | ZA842064B (fr) |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4832458A (en) * | 1984-08-28 | 1989-05-23 | Talig Corporation | Display for contrast enhancement |
US4732456A (en) * | 1984-08-28 | 1988-03-22 | Taliq Corporation | Scattering display for contrast enhancement including target |
US8110608B2 (en) | 2008-06-05 | 2012-02-07 | Ecolab Usa Inc. | Solid form sodium lauryl sulfate (SLS) pesticide composition |
US8968757B2 (en) | 2010-10-12 | 2015-03-03 | Ecolab Usa Inc. | Highly wettable, water dispersible, granules including two pesticides |
CN103396437B (zh) * | 2013-07-22 | 2015-09-09 | 衡阳师范学院 | 双(三环己基锡)二元羧酸酯及制备方法与应用 |
Family Cites Families (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
NL96805C (fr) * | 1957-11-18 | 1900-01-01 | ||
NL269911A (fr) * | 1960-10-04 | 1900-01-01 | ||
US3129236A (en) * | 1960-12-31 | 1964-04-14 | Monsanto Chemicals | Bis(trihydrocarbyl tin oxy) aromatic compounds |
NL299805A (fr) * | 1962-10-29 | 1900-01-01 | ||
US3264177A (en) * | 1964-02-17 | 1966-08-02 | Dow Chemical Co | Methods for the control of arachnids |
US3542824A (en) * | 1968-07-31 | 1970-11-24 | Dow Chemical Co | Perfluorocarboxylic acid ester of tricyclohexyltin hydroxide |
US3598849A (en) * | 1968-09-20 | 1971-08-10 | Dow Chemical Co | Tricyclohexyltin esters |
US3703588A (en) * | 1969-11-21 | 1972-11-21 | Norio Saito Nara Ken And Uniti | Method for imparting antistatic properties to polymeric materials |
US3861949A (en) * | 1971-04-27 | 1975-01-21 | Kureha Chemical Ind Co Ltd | Article having applied to the surface thereof, an anti-fouling composition comprising a polymer and an organo-tin compound |
US3790611A (en) * | 1972-10-05 | 1974-02-05 | M & T Chemicals Inc | Tris(cyclohexylalkyl)tin or hexakis(cyclohexylalkyl)tin compounds |
DE2419208A1 (de) * | 1974-04-18 | 1975-11-06 | Schering Ag | Mittel mit selektiver, herbizider und algizider wirkung |
FR2335514A1 (fr) * | 1975-12-17 | 1977-07-15 | M & T Chemicals Inc | Procede de preparation d'un derive de triorganoetain |
US4224338A (en) * | 1976-08-17 | 1980-09-23 | The Dow Chemical Company | Simultaneous fungicidal and miticidal protection of plants employing certain tin compounds |
-
1983
- 1983-03-22 FR FR8304884A patent/FR2543142B1/fr not_active Expired
-
1984
- 1984-02-29 DK DK1362/84A patent/DK136284D0/da not_active Application Discontinuation
- 1984-03-06 IL IL71165A patent/IL71165A0/xx unknown
- 1984-03-14 GR GR74100A patent/GR81825B/el unknown
- 1984-03-19 PH PH30411A patent/PH20025A/en unknown
- 1984-03-19 DE DE19843410064 patent/DE3410064A1/de not_active Withdrawn
- 1984-03-19 KR KR1019840001392A patent/KR840007808A/ko not_active Application Discontinuation
- 1984-03-20 GB GB08407153A patent/GB2136811B/en not_active Expired
- 1984-03-20 NZ NZ207559A patent/NZ207559A/en unknown
- 1984-03-20 ZA ZA842064A patent/ZA842064B/xx unknown
- 1984-03-20 IT IT47894/84A patent/IT1177597B/it active
- 1984-03-20 CA CA000449971A patent/CA1231716A/fr not_active Expired
- 1984-03-20 AU AU25919/84A patent/AU2591984A/en not_active Abandoned
- 1984-03-21 HU HU841132A patent/HUT33961A/hu unknown
- 1984-03-21 CH CH1438/84A patent/CH660365A5/fr not_active IP Right Cessation
- 1984-03-21 BR BR8401318A patent/BR8401318A/pt unknown
- 1984-03-21 NL NL8400893A patent/NL8400893A/nl not_active Application Discontinuation
- 1984-03-21 LU LU85259A patent/LU85259A1/fr unknown
- 1984-03-21 PT PT78291A patent/PT78291B/fr unknown
- 1984-03-21 ES ES530812A patent/ES530812A0/es active Granted
- 1984-03-21 JP JP59054120A patent/JPS59176296A/ja active Pending
- 1984-03-22 BE BE0/212613A patent/BE899225A/fr not_active IP Right Cessation
- 1984-03-22 US US06/592,353 patent/US4602945A/en not_active Expired - Fee Related
- 1984-03-22 OA OA58257A patent/OA07683A/fr unknown
Also Published As
Publication number | Publication date |
---|---|
DE3410064A1 (de) | 1984-09-27 |
GR81825B (fr) | 1984-12-12 |
BR8401318A (pt) | 1984-10-30 |
ZA842064B (en) | 1984-10-31 |
ES8506034A1 (es) | 1985-06-16 |
BE899225A (fr) | 1984-09-24 |
DK136284D0 (da) | 1984-02-29 |
GB2136811B (en) | 1986-07-09 |
NZ207559A (en) | 1985-12-13 |
ES530812A0 (es) | 1985-06-16 |
IL71165A0 (en) | 1984-06-29 |
PH20025A (en) | 1986-09-04 |
PT78291B (fr) | 1986-08-08 |
IT8447894A0 (it) | 1984-03-20 |
LU85259A1 (fr) | 1985-10-14 |
GB8407153D0 (en) | 1984-04-26 |
CH660365A5 (fr) | 1987-04-15 |
IT8447894A1 (it) | 1985-09-20 |
IT1177597B (it) | 1987-08-26 |
AU2591984A (en) | 1984-09-27 |
US4602945A (en) | 1986-07-29 |
GB2136811A (en) | 1984-09-26 |
PT78291A (fr) | 1984-04-01 |
OA07683A (fr) | 1985-05-23 |
JPS59176296A (ja) | 1984-10-05 |
HUT33961A (en) | 1985-01-28 |
KR840007808A (ko) | 1984-12-11 |
FR2543142A1 (fr) | 1984-09-28 |
CA1231716A (fr) | 1988-01-19 |
FR2543142B1 (fr) | 1986-01-03 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JP2552811B2 (ja) | 殺虫作用のあるフェニルヒドラジン誘導体 | |
US4128665A (en) | Substituted dinitrotrifluoromethyldiphenylamine and pesticidal compositions containing same | |
US3501578A (en) | Fungicidal composition containing phenyl - mercaptomethane-sulfonamide and method of using the same | |
JPS6245860B2 (fr) | ||
NL8702927A (nl) | Preparaten met fungicide werking en werkwijzen voor het bereiden en toepassen van deze preparaten. | |
NL8400893A (nl) | Organotinverbinding, werkwijze voor het bereiden daarvan, deze verbinding bevattende insecticide- en acaricidepreparaten en methode voor het bestrijden van fytofage insecten en acariden. | |
JPS6241564B2 (fr) | ||
DE4106509A1 (de) | Verwendung von oximetherderivaten zur bioregulation bei pflanzen | |
US5125959A (en) | Method of thinning lateral flowers of apples | |
US3088817A (en) | Method of controlling undesirable plant growth | |
JPS61200968A (ja) | 複素環式化合物、その製造方法およびこれを含有する、殺菌または植物生長調整剤組成物 | |
JPS62205063A (ja) | 新規な2−シアノベンゾイミダゾ−ル誘導体、その製造方法および殺菌剤としてのその使用、並びに他の殺菌剤との組合せ物 | |
US4804405A (en) | Elective herbicide compositions having a prolonged action containing .alpha. | |
CS261895B2 (en) | Agent for plants growth regulation and method of efficient substance production | |
US4385067A (en) | Fungicidal nitrilomethylidyne phenyl-acrylates and method of use | |
US4064262A (en) | S-methyl 3-furfurylidene-2-methyl-dithiocarbazate and its use as a fungicide | |
CA1204298A (fr) | Herbicide synergistique | |
US2935442A (en) | Method of protecting material against fungi comprising applying a heavy metal complex of a 1, 2-naphthoquinone 2-oxime | |
US4055640A (en) | Compositions and methods for controlling the growth of bacteria, fungi and algae using certain derivatives of N-(2,2-dichlorovinyl)salicylamides | |
JPS62207260A (ja) | 殺菌剤 | |
EA005858B1 (ru) | Инсектицидная композиция, обладающая улучшенной стойкостью при хранении | |
CZ121499A3 (cs) | Hydroximové a hydrazonové deriváty, způsob jejich přípravy a fungicidní prostředky, které je obsahují | |
US2899355A (en) | Fungicidal composition therefor | |
EP0230207B1 (fr) | Dérivé de triazine, sa préparation et son utilisation | |
CA1075248A (fr) | S-methyl 3-furfurylidene-2-methyl-dithiocarbazate; emploi comme fongicide |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
A85 | Still pending on 85-01-01 | ||
BV | The patent application has lapsed |