CH485412A - Mittel zur Bekämpfung tierischer und pflanzlicher Schädlinge - Google Patents
Mittel zur Bekämpfung tierischer und pflanzlicher SchädlingeInfo
- Publication number
- CH485412A CH485412A CH25470A CH2547067A CH485412A CH 485412 A CH485412 A CH 485412A CH 25470 A CH25470 A CH 25470A CH 2547067 A CH2547067 A CH 2547067A CH 485412 A CH485412 A CH 485412A
- Authority
- CH
- Switzerland
- Prior art keywords
- imidazole
- parts
- tribromo
- trichloro
- sep
- Prior art date
Links
- 241001465754 Metazoa Species 0.000 title claims description 9
- 241000607479 Yersinia pestis Species 0.000 title claims description 4
- 235000013311 vegetables Nutrition 0.000 title description 9
- 239000004480 active ingredient Substances 0.000 claims description 42
- 241000196324 Embryophyta Species 0.000 claims description 16
- 239000003795 chemical substances by application Substances 0.000 claims description 12
- 230000002363 herbicidal effect Effects 0.000 claims description 10
- 150000002460 imidazoles Chemical class 0.000 claims description 6
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 5
- 241000209140 Triticum Species 0.000 claims description 5
- 239000000969 carrier Substances 0.000 claims description 5
- 229910052717 sulfur Chemical group 0.000 claims description 5
- 239000011593 sulfur Chemical group 0.000 claims description 5
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 4
- 229910052760 oxygen Inorganic materials 0.000 claims description 4
- 239000001301 oxygen Substances 0.000 claims description 4
- 125000005843 halogen group Chemical group 0.000 claims description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 20
- -1 aliphatic hydrocarbon radical Chemical class 0.000 description 20
- 239000000839 emulsion Substances 0.000 description 15
- 239000012141 concentrate Substances 0.000 description 11
- 239000013543 active substance Substances 0.000 description 10
- 239000005995 Aluminium silicate Substances 0.000 description 9
- 241000238631 Hexapoda Species 0.000 description 9
- 235000012211 aluminium silicate Nutrition 0.000 description 9
- 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 9
- 239000000126 substance Substances 0.000 description 9
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 8
- 239000000203 mixture Substances 0.000 description 8
- 239000000843 powder Substances 0.000 description 8
- 239000000725 suspension Substances 0.000 description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
- 230000000895 acaricidal effect Effects 0.000 description 7
- 239000003995 emulsifying agent Substances 0.000 description 7
- 229920001223 polyethylene glycol Polymers 0.000 description 7
- 239000000377 silicon dioxide Substances 0.000 description 7
- 239000000243 solution Substances 0.000 description 7
- 239000002202 Polyethylene glycol Substances 0.000 description 6
- 239000000654 additive Substances 0.000 description 6
- 239000000428 dust Substances 0.000 description 6
- 150000001875 compounds Chemical class 0.000 description 5
- 229940079865 intestinal antiinfectives imidazole derivative Drugs 0.000 description 5
- 238000004519 manufacturing process Methods 0.000 description 5
- 229920000151 polyglycol Polymers 0.000 description 5
- 239000010695 polyglycol Substances 0.000 description 5
- 239000002904 solvent Substances 0.000 description 5
- JJYRORJLOMOBKX-UHFFFAOYSA-N 2,4,5-tribromo-1-(propan-2-yloxymethyl)imidazole Chemical compound C(C)(C)OCN1C(=NC(=C1Br)Br)Br JJYRORJLOMOBKX-UHFFFAOYSA-N 0.000 description 4
- PBBSWIMODGCGBB-UHFFFAOYSA-N 4,5-dibromo-2-chloro-1-(methoxymethyl)imidazole Chemical compound COCN1C(=NC(=C1Br)Br)Cl PBBSWIMODGCGBB-UHFFFAOYSA-N 0.000 description 4
- 241000238876 Acari Species 0.000 description 4
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 4
- 241001454295 Tetranychidae Species 0.000 description 4
- 241001454293 Tetranychus urticae Species 0.000 description 4
- 235000021307 Triticum Nutrition 0.000 description 4
- 239000002253 acid Substances 0.000 description 4
- 235000019993 champagne Nutrition 0.000 description 4
- 230000001276 controlling effect Effects 0.000 description 4
- 239000002270 dispersing agent Substances 0.000 description 4
- 239000008187 granular material Substances 0.000 description 4
- 230000000749 insecticidal effect Effects 0.000 description 4
- 159000000000 sodium salts Chemical class 0.000 description 4
- 239000007787 solid Substances 0.000 description 4
- 239000000758 substrate Substances 0.000 description 4
- 239000000454 talc Substances 0.000 description 4
- 229910052623 talc Inorganic materials 0.000 description 4
- 239000004563 wettable powder Substances 0.000 description 4
- 239000008096 xylene Substances 0.000 description 4
- YNRHCFIOLPTWEW-UHFFFAOYSA-N 2,4,5-trichloro-1-(methoxymethyl)imidazole Chemical compound COCN1C(=NC(=C1Cl)Cl)Cl YNRHCFIOLPTWEW-UHFFFAOYSA-N 0.000 description 3
- GXJHZYXSFORYPX-UHFFFAOYSA-N 2,4,5-trichloro-1-(propoxymethyl)imidazole Chemical compound C(CC)OCN1C(=NC(=C1Cl)Cl)Cl GXJHZYXSFORYPX-UHFFFAOYSA-N 0.000 description 3
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 3
- 241000254173 Coleoptera Species 0.000 description 3
- 241000255925 Diptera Species 0.000 description 3
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 3
- 241000257226 Muscidae Species 0.000 description 3
- 235000011941 Tilia x europaea Nutrition 0.000 description 3
- DNEHKUCSURWDGO-UHFFFAOYSA-N aluminum sodium Chemical compound [Na].[Al] DNEHKUCSURWDGO-UHFFFAOYSA-N 0.000 description 3
- 235000013339 cereals Nutrition 0.000 description 3
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
- 235000013399 edible fruits Nutrition 0.000 description 3
- 150000002191 fatty alcohols Chemical class 0.000 description 3
- 239000004615 ingredient Substances 0.000 description 3
- 239000004571 lime Substances 0.000 description 3
- 229920006395 saturated elastomer Polymers 0.000 description 3
- 239000007921 spray Substances 0.000 description 3
- YFXDMMDCUGCCGY-UHFFFAOYSA-N 2,4,5-tribromo-1-(methoxymethyl)imidazole Chemical compound COCN1C(Br)=NC(Br)=C1Br YFXDMMDCUGCCGY-UHFFFAOYSA-N 0.000 description 2
- MNFDIPKRZDEUMN-UHFFFAOYSA-N 2,4,5-tribromo-1-(propoxymethyl)imidazole Chemical compound C(CC)OCN1C(=NC(=C1Br)Br)Br MNFDIPKRZDEUMN-UHFFFAOYSA-N 0.000 description 2
- JCGGPCDDFXIVQB-UHFFFAOYSA-N 2,4,5-tribromo-1h-imidazole Chemical class BrC1=NC(Br)=C(Br)N1 JCGGPCDDFXIVQB-UHFFFAOYSA-N 0.000 description 2
- XPLCFBYKEIVOPW-UHFFFAOYSA-N 2,4,5-trichloro-1-(propan-2-yloxymethyl)imidazole Chemical compound CC(C)OCN1C(Cl)=NC(Cl)=C1Cl XPLCFBYKEIVOPW-UHFFFAOYSA-N 0.000 description 2
- WBIQQQGBSDOWNP-UHFFFAOYSA-N 2-dodecylbenzenesulfonic acid Chemical compound CCCCCCCCCCCCC1=CC=CC=C1S(O)(=O)=O WBIQQQGBSDOWNP-UHFFFAOYSA-N 0.000 description 2
- VWEQSMMFLDYVHH-UHFFFAOYSA-N 4,5-dibromo-2-chloro-1-(propan-2-ylsulfanylmethyl)imidazole Chemical compound C(C)(C)SCN1C(=NC(=C1Br)Br)Cl VWEQSMMFLDYVHH-UHFFFAOYSA-N 0.000 description 2
- WPGPOYRQEZIAAG-UHFFFAOYSA-N 4,5-dibromo-2-chloro-1-(propoxymethyl)imidazole Chemical compound C(CC)OCN1C(=NC(=C1Br)Br)Cl WPGPOYRQEZIAAG-UHFFFAOYSA-N 0.000 description 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- 241000256111 Aedes <genus> Species 0.000 description 2
- 241000239223 Arachnida Species 0.000 description 2
- 241000239290 Araneae Species 0.000 description 2
- 241000238662 Blatta orientalis Species 0.000 description 2
- AQUUDERUHHAECG-UHFFFAOYSA-N C(C)(C)SCN1C(=NC(=C1Br)Br)Br Chemical compound C(C)(C)SCN1C(=NC(=C1Br)Br)Br AQUUDERUHHAECG-UHFFFAOYSA-N 0.000 description 2
- LOAHFMZLAONMDI-UHFFFAOYSA-N CSCN1C(Cl)=NC(Br)=C1Br Chemical compound CSCN1C(Cl)=NC(Br)=C1Br LOAHFMZLAONMDI-UHFFFAOYSA-N 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- 240000005979 Hordeum vulgare Species 0.000 description 2
- 235000007340 Hordeum vulgare Nutrition 0.000 description 2
- 239000005909 Kieselgur Substances 0.000 description 2
- 241000254022 Locusta migratoria Species 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- 241000205407 Polygonum Species 0.000 description 2
- 239000004372 Polyvinyl alcohol Substances 0.000 description 2
- 125000002877 alkyl aryl group Chemical group 0.000 description 2
- UKXSKSHDVLQNKG-UHFFFAOYSA-N benzilic acid Chemical class C=1C=CC=CC=1C(O)(C(=O)O)C1=CC=CC=C1 UKXSKSHDVLQNKG-UHFFFAOYSA-N 0.000 description 2
- 235000021028 berry Nutrition 0.000 description 2
- 239000011230 binding agent Substances 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 2
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
- SWXVUIWOUIDPGS-UHFFFAOYSA-N diacetone alcohol Chemical compound CC(=O)CC(C)(C)O SWXVUIWOUIDPGS-UHFFFAOYSA-N 0.000 description 2
- 229940060296 dodecylbenzenesulfonic acid Drugs 0.000 description 2
- 235000013601 eggs Nutrition 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 150000002170 ethers Chemical class 0.000 description 2
- 235000013312 flour Nutrition 0.000 description 2
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Substances C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 description 2
- 239000002917 insecticide Substances 0.000 description 2
- 229920005610 lignin Polymers 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- 125000000913 palmityl 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])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 2
- 239000000575 pesticide Substances 0.000 description 2
- 239000003209 petroleum derivative Substances 0.000 description 2
- 230000008635 plant growth Effects 0.000 description 2
- 229920002451 polyvinyl alcohol Polymers 0.000 description 2
- 150000004760 silicates Chemical class 0.000 description 2
- 230000009885 systemic effect Effects 0.000 description 2
- ALSTYHKOOCGGFT-KTKRTIGZSA-N (9Z)-octadecen-1-ol Chemical compound CCCCCCCC\C=C/CCCCCCCCO ALSTYHKOOCGGFT-KTKRTIGZSA-N 0.000 description 1
- DGKXRRIUWDMTNX-UHFFFAOYSA-N 2,4,5-tribromo-1-(2-methylpropoxymethyl)imidazole Chemical compound C(C(C)C)OCN1C(=NC(=C1Br)Br)Br DGKXRRIUWDMTNX-UHFFFAOYSA-N 0.000 description 1
- JERQKRUBRQQLRR-UHFFFAOYSA-N 2,4,5-tribromo-1-(butoxymethyl)imidazole Chemical compound C(CCC)OCN1C(=NC(=C1Br)Br)Br JERQKRUBRQQLRR-UHFFFAOYSA-N 0.000 description 1
- VSMMZLUXWOZHMK-UHFFFAOYSA-N 2,4,5-tribromo-1-(butylsulfanylmethyl)imidazole Chemical compound C(CCC)SCN1C(=NC(=C1Br)Br)Br VSMMZLUXWOZHMK-UHFFFAOYSA-N 0.000 description 1
- DNIQDGBXXYXPGR-UHFFFAOYSA-N 2,4,5-tribromo-1-(methylsulfanylmethyl)imidazole Chemical compound CSCN1C(=NC(=C1Br)Br)Br DNIQDGBXXYXPGR-UHFFFAOYSA-N 0.000 description 1
- VDEPSSNQSCCTJO-UHFFFAOYSA-N 2,4,5-tribromo-1-(propylsulfanylmethyl)imidazole Chemical compound CCCSCN1C(Br)=NC(Br)=C1Br VDEPSSNQSCCTJO-UHFFFAOYSA-N 0.000 description 1
- FCFQBSFFWBHUQI-UHFFFAOYSA-N 2,4,5-trichloro-1-(ethoxymethyl)imidazole Chemical compound CCOCN1C(Cl)=NC(Cl)=C1Cl FCFQBSFFWBHUQI-UHFFFAOYSA-N 0.000 description 1
- OCVXSFKKWXMYPF-UHFFFAOYSA-N 2-chloroimidazole Chemical compound ClC1=NC=CN1 OCVXSFKKWXMYPF-UHFFFAOYSA-N 0.000 description 1
- 125000001731 2-cyanoethyl group Chemical group [H]C([H])(*)C([H])([H])C#N 0.000 description 1
- 241001143309 Acanthoscelides obtectus Species 0.000 description 1
- 241000256118 Aedes aegypti Species 0.000 description 1
- 241000489242 Amphitetranychus viennensis Species 0.000 description 1
- 241001414900 Anopheles stephensi Species 0.000 description 1
- 241001124076 Aphididae Species 0.000 description 1
- 241001425390 Aphis fabae Species 0.000 description 1
- 241000238660 Blattidae Species 0.000 description 1
- 241001674044 Blattodea Species 0.000 description 1
- 241001388466 Bruchus rufimanus Species 0.000 description 1
- 241000488564 Bryobia Species 0.000 description 1
- 241001260012 Bursa Species 0.000 description 1
- FIPWRIJSWJWJAI-UHFFFAOYSA-N Butyl carbitol 6-propylpiperonyl ether Chemical compound C1=C(CCC)C(COCCOCCOCCCC)=CC2=C1OCO2 FIPWRIJSWJWJAI-UHFFFAOYSA-N 0.000 description 1
- YUIZURZERANZQY-UHFFFAOYSA-N C(C)SCN1C(=NC(=C1Cl)Cl)Cl Chemical compound C(C)SCN1C(=NC(=C1Cl)Cl)Cl YUIZURZERANZQY-UHFFFAOYSA-N 0.000 description 1
- PZLXKLHGTFTZGT-UHFFFAOYSA-N C(C=CC)OCN1C(=NC(=C1Br)Br)Br Chemical compound C(C=CC)OCN1C(=NC(=C1Br)Br)Br PZLXKLHGTFTZGT-UHFFFAOYSA-N 0.000 description 1
- RFTGUQFFTZWXJA-UHFFFAOYSA-N C(CCC)OCN1C(=NC(=C1Cl)Cl)Cl Chemical compound C(CCC)OCN1C(=NC(=C1Cl)Cl)Cl RFTGUQFFTZWXJA-UHFFFAOYSA-N 0.000 description 1
- LUGMDFOCHYNFEU-UHFFFAOYSA-N CC(C)(C)SCN1C(Cl)=NC(Br)=C1Br Chemical compound CC(C)(C)SCN1C(Cl)=NC(Br)=C1Br LUGMDFOCHYNFEU-UHFFFAOYSA-N 0.000 description 1
- QOTSWLDDMBLRKT-UHFFFAOYSA-N CC(C)COCN1C(Cl)=NC(Cl)=C1Cl Chemical compound CC(C)COCN1C(Cl)=NC(Cl)=C1Cl QOTSWLDDMBLRKT-UHFFFAOYSA-N 0.000 description 1
- RHMAIRRSFBYANJ-UHFFFAOYSA-N CC(C)SCN1C(Cl)=NC(Cl)=C1Cl Chemical compound CC(C)SCN1C(Cl)=NC(Cl)=C1Cl RHMAIRRSFBYANJ-UHFFFAOYSA-N 0.000 description 1
- MQTNRDPMAUIANG-UHFFFAOYSA-N CCC(C)OCN1C(Cl)=NC(Cl)=C1Cl Chemical compound CCC(C)OCN1C(Cl)=NC(Cl)=C1Cl MQTNRDPMAUIANG-UHFFFAOYSA-N 0.000 description 1
- LWVQURAAMIQTDY-UHFFFAOYSA-N CCC(C)SCN1C(Br)=NC(Br)=C1Br Chemical compound CCC(C)SCN1C(Br)=NC(Br)=C1Br LWVQURAAMIQTDY-UHFFFAOYSA-N 0.000 description 1
- ZAZUYYCOEDCDKA-UHFFFAOYSA-N CCSCN1C(Cl)=NC(Br)=C1Br Chemical compound CCSCN1C(Cl)=NC(Br)=C1Br ZAZUYYCOEDCDKA-UHFFFAOYSA-N 0.000 description 1
- 241000220244 Capsella <angiosperm> Species 0.000 description 1
- 240000006122 Chenopodium album Species 0.000 description 1
- 235000009344 Chenopodium album Nutrition 0.000 description 1
- 241000256057 Culex quinquefasciatus Species 0.000 description 1
- 241000256113 Culicidae Species 0.000 description 1
- 241000254171 Curculionidae Species 0.000 description 1
- 241001641896 Dermestes lardarius Species 0.000 description 1
- 241001513837 Dermestes maculatus Species 0.000 description 1
- 241000131287 Dermestidae Species 0.000 description 1
- 241000630736 Ephestia Species 0.000 description 1
- 241000122098 Ephestia kuehniella Species 0.000 description 1
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 description 1
- 241001232715 Granaria Species 0.000 description 1
- 241000257303 Hymenoptera Species 0.000 description 1
- 241000258916 Leptinotarsa decemlineata Species 0.000 description 1
- 241000209082 Lolium Species 0.000 description 1
- 241001481698 Mesostigmata Species 0.000 description 1
- 241000257159 Musca domestica Species 0.000 description 1
- 241000275031 Nica Species 0.000 description 1
- IGFHQQFPSIBGKE-UHFFFAOYSA-N Nonylphenol Natural products CCCCCCCCCC1=CC=C(O)C=C1 IGFHQQFPSIBGKE-UHFFFAOYSA-N 0.000 description 1
- 241000238814 Orthoptera Species 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 208000002193 Pain Diseases 0.000 description 1
- 235000019483 Peanut oil Nutrition 0.000 description 1
- 244000046052 Phaseolus vulgaris Species 0.000 description 1
- 235000010627 Phaseolus vulgaris Nutrition 0.000 description 1
- ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical compound OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 description 1
- 241001674048 Phthiraptera Species 0.000 description 1
- 241000691880 Planococcus citri Species 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 241001415279 Pseudococcidae Species 0.000 description 1
- 241000255893 Pyralidae Species 0.000 description 1
- 235000002357 Ribes grossularia Nutrition 0.000 description 1
- 244000171263 Ribes grossularia Species 0.000 description 1
- 241001645405 Sarcoptiformes Species 0.000 description 1
- 241000220261 Sinapis Species 0.000 description 1
- 241000254181 Sitophilus Species 0.000 description 1
- 244000061456 Solanum tuberosum Species 0.000 description 1
- 235000002595 Solanum tuberosum Nutrition 0.000 description 1
- 244000062793 Sorghum vulgare Species 0.000 description 1
- 241001494115 Stomoxys calcitrans Species 0.000 description 1
- 241000254109 Tenebrio molitor Species 0.000 description 1
- 241000254107 Tenebrionidae Species 0.000 description 1
- 241001645411 Trombidiformes Species 0.000 description 1
- VXSIXFKKSNGRRO-MXOVTSAMSA-N [(1s)-2-methyl-4-oxo-3-[(2z)-penta-2,4-dienyl]cyclopent-2-en-1-yl] (1r,3r)-2,2-dimethyl-3-(2-methylprop-1-enyl)cyclopropane-1-carboxylate;[(1s)-2-methyl-4-oxo-3-[(2z)-penta-2,4-dienyl]cyclopent-2-en-1-yl] (1r,3r)-3-[(e)-3-methoxy-2-methyl-3-oxoprop-1-enyl Chemical class CC1(C)[C@H](C=C(C)C)[C@H]1C(=O)O[C@@H]1C(C)=C(C\C=C/C=C)C(=O)C1.CC1(C)[C@H](/C=C(\C)C(=O)OC)[C@H]1C(=O)O[C@@H]1C(C)=C(C\C=C/C=C)C(=O)C1 VXSIXFKKSNGRRO-MXOVTSAMSA-N 0.000 description 1
- BUJHNFUAPWGZDP-UHFFFAOYSA-N [P].[Ca].[Ca].[Ca] Chemical compound [P].[Ca].[Ca].[Ca] BUJHNFUAPWGZDP-UHFFFAOYSA-N 0.000 description 1
- 239000000642 acaricide Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 150000001447 alkali salts Chemical class 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 239000010775 animal oil Substances 0.000 description 1
- 230000000844 anti-bacterial effect Effects 0.000 description 1
- 239000007900 aqueous suspension Substances 0.000 description 1
- 125000003118 aryl group Chemical group 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
- OKVYEXCEUZCQEH-UHFFFAOYSA-N benzenesulfonic acid;formaldehyde;naphthalene-1-sulfonic acid Chemical compound O=C.OS(=O)(=O)C1=CC=CC=C1.C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 OKVYEXCEUZCQEH-UHFFFAOYSA-N 0.000 description 1
- 229940087675 benzilic acid Drugs 0.000 description 1
- 230000003115 biocidal effect Effects 0.000 description 1
- 239000008280 blood Substances 0.000 description 1
- 210000004369 blood Anatomy 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 159000000007 calcium salts Chemical class 0.000 description 1
- 244000309466 calf Species 0.000 description 1
- 229940112021 centrally acting muscle relaxants carbamic acid ester Drugs 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 235000020971 citrus fruits Nutrition 0.000 description 1
- 210000000078 claw Anatomy 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 239000007799 cork Substances 0.000 description 1
- 244000038559 crop plants Species 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- ZZTMMVAAULUFCS-UHFFFAOYSA-L disodium;methanedisulfonate Chemical compound [Na+].[Na+].[O-]S(=O)(=O)CS([O-])(=O)=O ZZTMMVAAULUFCS-UHFFFAOYSA-L 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000003337 fertilizer Substances 0.000 description 1
- QJAUKMLCDVOYNX-UHFFFAOYSA-N formaldehyde;2-hydroxybenzenesulfonic acid Chemical compound O=C.OC1=CC=CC=C1S(O)(=O)=O QJAUKMLCDVOYNX-UHFFFAOYSA-N 0.000 description 1
- NVVZQXQBYZPMLJ-UHFFFAOYSA-N formaldehyde;naphthalene-1-sulfonic acid Chemical compound O=C.C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 NVVZQXQBYZPMLJ-UHFFFAOYSA-N 0.000 description 1
- 230000000855 fungicidal effect Effects 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 238000011081 inoculation Methods 0.000 description 1
- 230000001418 larval effect Effects 0.000 description 1
- 235000019713 millet Nutrition 0.000 description 1
- 239000002480 mineral oil Substances 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
- 230000001069 nematicidal effect Effects 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
- 235000019198 oils Nutrition 0.000 description 1
- 229940055577 oleyl alcohol Drugs 0.000 description 1
- XMLQWXUVTXCDDL-UHFFFAOYSA-N oleyl alcohol Natural products CCCCCCC=CCCCCCCCCCCO XMLQWXUVTXCDDL-UHFFFAOYSA-N 0.000 description 1
- 125000001117 oleyl 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])=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
- 239000004006 olive oil Substances 0.000 description 1
- 235000008390 olive oil Nutrition 0.000 description 1
- 239000000312 peanut oil Substances 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 239000000546 pharmaceutical excipient Substances 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 150000003014 phosphoric acid esters Chemical class 0.000 description 1
- 230000000885 phytotoxic effect Effects 0.000 description 1
- 229960005235 piperonyl butoxide Drugs 0.000 description 1
- 235000021018 plums Nutrition 0.000 description 1
- 238000006068 polycondensation reaction Methods 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 238000004382 potting Methods 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 235000021251 pulses Nutrition 0.000 description 1
- HYJYGLGUBUDSLJ-UHFFFAOYSA-N pyrethrin Natural products CCC(=O)OC1CC(=C)C2CC3OC3(C)C2C2OC(=O)C(=C)C12 HYJYGLGUBUDSLJ-UHFFFAOYSA-N 0.000 description 1
- 229940070846 pyrethrins Drugs 0.000 description 1
- 239000002728 pyrethroid Substances 0.000 description 1
- 150000003254 radicals Chemical class 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 230000000284 resting effect Effects 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- RPACBEVZENYWOL-XFULWGLBSA-M sodium;(2r)-2-[6-(4-chlorophenoxy)hexyl]oxirane-2-carboxylate Chemical compound [Na+].C=1C=C(Cl)C=CC=1OCCCCCC[C@]1(C(=O)[O-])CO1 RPACBEVZENYWOL-XFULWGLBSA-M 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
- 239000002689 soil Substances 0.000 description 1
- 238000009331 sowing Methods 0.000 description 1
- 239000004575 stone Substances 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 125000004434 sulfur atom Chemical group 0.000 description 1
- 150000003470 sulfuric acid monoesters Chemical class 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 235000013619 trace mineral Nutrition 0.000 description 1
- 239000011573 trace mineral Substances 0.000 description 1
- JOYRKODLDBILNP-UHFFFAOYSA-N urethane group Chemical group NC(=O)OCC JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 238000010626 work up procedure Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/66—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D233/68—Halogen atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Plural Heterocyclic Compounds (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH25470A CH485412A (de) | 1967-04-26 | 1967-04-26 | Mittel zur Bekämpfung tierischer und pflanzlicher Schädlinge |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH596067A CH485733A (de) | 1967-04-26 | 1967-04-26 | Verfahren zur Herstellung halogensubstituierter Imidazol-Derivate |
| CH25470A CH485412A (de) | 1967-04-26 | 1967-04-26 | Mittel zur Bekämpfung tierischer und pflanzlicher Schädlinge |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CH485412A true CH485412A (de) | 1970-02-15 |
Family
ID=4302145
Family Applications (3)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH25470A CH485412A (de) | 1967-04-26 | 1967-04-26 | Mittel zur Bekämpfung tierischer und pflanzlicher Schädlinge |
| CH596067A CH485733A (de) | 1967-04-26 | 1967-04-26 | Verfahren zur Herstellung halogensubstituierter Imidazol-Derivate |
| CH25370A CH485736A (de) | 1967-04-26 | 1967-04-26 | Verfahren zur Herstellung halogensubstituierter Imidazol-Derivate |
Family Applications After (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH596067A CH485733A (de) | 1967-04-26 | 1967-04-26 | Verfahren zur Herstellung halogensubstituierter Imidazol-Derivate |
| CH25370A CH485736A (de) | 1967-04-26 | 1967-04-26 | Verfahren zur Herstellung halogensubstituierter Imidazol-Derivate |
Country Status (14)
| Country | Link |
|---|---|
| US (5) | US3625953A (esLanguage) |
| AT (4) | AT280280B (esLanguage) |
| BE (3) | BE714239A (esLanguage) |
| BR (1) | BR6898630D0 (esLanguage) |
| CA (1) | CA928306A (esLanguage) |
| CH (3) | CH485412A (esLanguage) |
| DE (2) | DE1770270A1 (esLanguage) |
| DK (2) | DK125565B (esLanguage) |
| ES (6) | ES353179A1 (esLanguage) |
| FR (3) | FR1567372A (esLanguage) |
| GB (3) | GB1197103A (esLanguage) |
| IL (3) | IL29887A (esLanguage) |
| NL (3) | NL139313B (esLanguage) |
| SE (3) | SE352804B (esLanguage) |
Families Citing this family (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CH485412A (de) * | 1967-04-26 | 1970-02-15 | Agripat Sa | Mittel zur Bekämpfung tierischer und pflanzlicher Schädlinge |
| CH510394A (de) * | 1969-07-04 | 1971-07-31 | Ciba Geigy Ag | Akarizides Mittel |
| FR2104652A2 (en) * | 1970-04-29 | 1972-04-21 | Agripat Sa | 1-alkoxymethyl-2, 4, 5-trichloroimidazoles - insecticides and acaricides |
| US3934019A (en) * | 1970-12-18 | 1976-01-20 | Bayer Aktiengesellschaft | Pesticidal 4,5-bis-(trifluoromethylimino)-diazoles |
| US4089672A (en) * | 1972-12-20 | 1978-05-16 | The Upjohn Company | 1-(Substituted-hydrocarbyl)-di- and trihalopyrazoles |
| DE2314985A1 (de) * | 1973-03-26 | 1974-10-17 | Hoechst Ag | 1-(imidazol-1-yl)-isochinoline und verfahren zu ihrer herstellung |
| NZ178996A (en) * | 1974-11-15 | 1978-06-02 | Kornis G | Pyrfazole amides and thioamides;herbicidal compositions |
| AU2241677A (en) * | 1976-03-12 | 1978-08-24 | Bayer Ag | 4,5-dichloroimidazole-2-carboxylic acid derivatives |
| DE2646144A1 (de) * | 1976-10-13 | 1978-04-20 | Bayer Ag | 4,5-dichlor-imidazol-derivate, verfahren zu ihrer herstellung sowie ihre verwendung als pflanzenschutzmittel |
| US4185991A (en) * | 1976-10-13 | 1980-01-29 | Bayer Aktiengesellschaft | 4,5-Dichloro-imidazole derivatives and their use as herbicides |
| US4187100A (en) * | 1976-10-13 | 1980-02-05 | Bayer Aktiengesellschaft | 4,5-Dichloro-imidazole-1-carboxylic acid aryl esters and their use as herbicides |
| DE2646143A1 (de) * | 1976-10-13 | 1978-04-20 | Bayer Ag | 4,5-dichlor-imidazol-1-carbonsaeure- arylester, verfahren zu ihrer herstellung sowie ihre verwendung als pflanzenschutzmittel |
| DE2646142A1 (de) * | 1976-10-13 | 1978-04-20 | Bayer Ag | 1-acyloxymethyl-4,5-dichlor- imidazol-2-carbonsaeure-derivate, verfahren zu ihrer herstellung sowie ihre verwendung als pflanzenschutzmittel |
| EG17668A (en) * | 1984-11-22 | 1990-08-30 | Sumitomo Chemical Co | Process for preparing of a bromodichlorimidazole insecticide |
| JPS6239577A (ja) * | 1985-08-15 | 1987-02-20 | Sumitomo Chem Co Ltd | トリハロイミダゾ−ル誘導体、その製造法およびそれを有効成分とする殺虫剤 |
| DE3828208A1 (de) * | 1988-08-19 | 1990-02-22 | Basf Ag | Substituierte 2-chlorimidazolderivate, verfahren zu ihrer herstellung sowie ihre verwendung als herbizide mittel |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1567084A1 (de) * | 1963-07-01 | 1970-10-15 | Shell Int Research | Mittel zur Bekaempfung unerwuenschten Pflanzenwuchses |
| US3501286A (en) * | 1964-06-29 | 1970-03-17 | Shell Oil Co | Plant growth control |
| DE1294086B (de) * | 1964-08-07 | 1969-04-30 | Shell Int Research | Herbizide Mittel |
| GB1154722A (en) * | 1965-07-08 | 1969-06-11 | Boots Pure Drug Co Ltd | 2,4,5-Tribromoimidazole Derivatives and Compositions thereof |
| US3409606A (en) * | 1965-12-30 | 1968-11-05 | American Cyanamid Co | Halogenated chloroimidazole compounds |
| US3435050A (en) * | 1966-04-08 | 1969-03-25 | Dow Chemical Co | 2,4,5-trichloroimidazole and method of preparation |
| FR1494338A (fr) * | 1966-07-29 | 1967-09-08 | Chimetron Sarl | Sulfénylimidazoles |
| CH485412A (de) * | 1967-04-26 | 1970-02-15 | Agripat Sa | Mittel zur Bekämpfung tierischer und pflanzlicher Schädlinge |
-
1967
- 1967-04-26 CH CH25470A patent/CH485412A/de not_active IP Right Cessation
- 1967-04-26 CH CH596067A patent/CH485733A/de not_active IP Right Cessation
- 1967-04-26 CH CH25370A patent/CH485736A/de not_active IP Right Cessation
-
1968
- 1968-04-24 US US723903A patent/US3625953A/en not_active Expired - Lifetime
- 1968-04-24 US US723904A patent/US3625955A/en not_active Expired - Lifetime
- 1968-04-25 IL IL29887A patent/IL29887A/en unknown
- 1968-04-25 CA CA018359A patent/CA928306A/en not_active Expired
- 1968-04-25 GB GB19571/68A patent/GB1197103A/en not_active Expired
- 1968-04-25 BE BE714239D patent/BE714239A/xx unknown
- 1968-04-25 ES ES353179A patent/ES353179A1/es not_active Expired
- 1968-04-25 ES ES353177A patent/ES353177A1/es not_active Expired
- 1968-04-25 IL IL29888A patent/IL29888A/xx unknown
- 1968-04-25 ES ES353182A patent/ES353182A1/es not_active Expired
- 1968-04-25 GB GB19569/68A patent/GB1197101A/en not_active Expired
- 1968-04-25 DE DE19681770270 patent/DE1770270A1/de active Pending
- 1968-04-25 GB GB19570/68A patent/GB1197102A/en not_active Expired
- 1968-04-25 AT AT404068A patent/AT280280B/de active
- 1968-04-25 BE BE714241D patent/BE714241A/xx unknown
- 1968-04-25 ES ES353178A patent/ES353178A1/es not_active Expired
- 1968-04-25 AT AT492969A patent/AT291667B/de not_active IP Right Cessation
- 1968-04-25 NL NL686805901A patent/NL139313B/xx unknown
- 1968-04-25 IL IL29886A patent/IL29886A/xx unknown
- 1968-04-25 FR FR1567372D patent/FR1567372A/fr not_active Expired
- 1968-04-25 SE SE05586/68A patent/SE352804B/xx unknown
- 1968-04-25 BR BR198630/68A patent/BR6898630D0/pt unknown
- 1968-04-25 SE SE05585/68A patent/SE354072B/xx unknown
- 1968-04-25 AT AT403968A patent/AT280279B/de not_active IP Right Cessation
- 1968-04-25 ES ES353180A patent/ES353180A1/es not_active Expired
- 1968-04-25 BE BE714240D patent/BE714240A/xx unknown
- 1968-04-25 DK DK189168AA patent/DK125565B/da unknown
- 1968-04-25 AT AT404168A patent/AT280692B/de not_active IP Right Cessation
- 1968-04-25 NL NL6805899A patent/NL6805899A/xx unknown
- 1968-04-25 SE SE05584/68A patent/SE354176B/xx unknown
- 1968-04-25 FR FR1567373D patent/FR1567373A/fr not_active Expired
- 1968-04-25 ES ES353181A patent/ES353181A1/es not_active Expired
- 1968-04-25 FR FR1567374D patent/FR1567374A/fr not_active Expired
- 1968-04-25 DK DK189368AA patent/DK125284B/da unknown
- 1968-04-25 NL NL6805900A patent/NL6805900A/xx unknown
- 1968-04-25 DE DE1770269A patent/DE1770269C3/de not_active Expired
-
1970
- 1970-06-08 US US44558A patent/US3674874A/en not_active Expired - Lifetime
-
1971
- 1971-04-05 US US00131447A patent/US3773960A/en not_active Expired - Lifetime
- 1971-06-28 US US00157698A patent/US3759945A/en not_active Expired - Lifetime
Also Published As
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CH485412A (de) | Mittel zur Bekämpfung tierischer und pflanzlicher Schädlinge | |
| EP0003211B1 (de) | Verfahren zur Bekämpfung von Insekten mit Imidazolderivaten | |
| DE2052379C3 (de) | O-(N-Alkoxy-benzimidoyl)-(thiono)phosphor(phosphon)saureester, Verfahren zu ihrer Herstellung sowie ihre Verwendung als Insektizide und Akarizide | |
| DE2447735A1 (de) | Spiro-cyclopropane, verfahren zu ihrer herstellung und ihre verwendung zur schaedlingsbekaempfung | |
| DE1670836A1 (de) | Verfahren zur Herstellung von Phosphon- bzw. Thionophosphonsaeureestern | |
| DE1443933C2 (de) | Thiocyano-phenyl-isothiocyanate und ihre Verwendung als Schädlingsbekämpfungsmittel | |
| DE1568019A1 (de) | Neue Carbaminsaeureester und Verfahren zu deren Herstellung | |
| DE1955749A1 (de) | Amidophenylguanidine,Verfahren zu ihrer Herstellung und ihre fungizide Verwendung | |
| DE1148806B (de) | Schaedlingsbekaempfungsmittel | |
| DE1181200B (de) | Verfahren zur Herstellung des N-Mono-methylamids der O, O-Di-(ª-fluoraethyl)-dithiophosphorylessigsaeure | |
| DE3638631A1 (de) | Pyrazoline, ihre herstellung und ihre verwendung als mittel mit insektizider und akarizider wirkung | |
| DE1161078B (de) | Mittel zur Bekaempfung von Insekten, Spinnen und Milben, deren Eiern und von Pilzen | |
| DE1767314A1 (de) | Insektizides und akarizides Mittel | |
| DE1542798C3 (de) | Pyrazolderivate und deren Verwendung | |
| EP0018578A2 (de) | 1,3-Benzodithiol-2-one, Verfahren zu ihrer Herstellung, diese Verbindungen enthaltende Mittel und ihre Verwendung zur Bekämpfung von Schädlingen sowie ihre Ausgangsprodukte | |
| DE1568019C (de) | Carbaminsäureester und Verfahren zu ihrer Herstellung | |
| DE1937476C (de) | Basisch substituierte 1 Cyano O carbamoyl formoxime, Verfahren zu deren Herstellung und diese Verbindungen ent haltende Schädlingsbekämpfungsmittel | |
| DE2003333A1 (de) | Mittel zur Bekaempfung von Insekten und Spinntieren und deren Entwicklungsstadien | |
| AT265743B (de) | Schädlingsbekämpfungsmittel | |
| AT253861B (de) | Insektizide Mischung | |
| DE1768555C3 (de) | Indanyl-N-methylcarbaminsäureester | |
| DE1642294C (de) | Insektizide, mitizide und fungizide Mittel | |
| DE2236459A1 (de) | Thiadiazolderivate als wirkstoffe in schaedlingsbekaempfungsmitteln | |
| DE3715872A1 (de) | Organische zinnverbindungen, ihre herstellung und ihre verwendung als insektizide und akarizide mittel | |
| DE2016678A1 (de) | Carbo-beta-Fluoräthoxyverbindungen, ihre Herstellung und ihre Verwendung in Schädlingsbekämpfungsmitteln |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PL | Patent ceased |