DE2128700C2 - Fungitoxische Mittel - Google Patents
Fungitoxische MittelInfo
- Publication number
- DE2128700C2 DE2128700C2 DE2128700A DE2128700A DE2128700C2 DE 2128700 C2 DE2128700 C2 DE 2128700C2 DE 2128700 A DE2128700 A DE 2128700A DE 2128700 A DE2128700 A DE 2128700A DE 2128700 C2 DE2128700 C2 DE 2128700C2
- Authority
- DE
- Germany
- Prior art keywords
- active ingredient
- plants
- weight
- active ingredients
- infestation
- Prior art date
- Legal status (The legal status 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 status listed.)
- Expired
Links
- 230000002464 fungitoxic effect Effects 0.000 title description 6
- 231100000162 fungitoxic Toxicity 0.000 title description 5
- 241000233866 Fungi Species 0.000 claims description 10
- 125000000217 alkyl group Chemical group 0.000 claims description 6
- 125000004432 carbon atom Chemical group C* 0.000 claims description 6
- 241000894006 Bacteria Species 0.000 claims description 5
- 229910052739 hydrogen Inorganic materials 0.000 claims description 5
- 239000001257 hydrogen Substances 0.000 claims description 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 4
- 150000003839 salts Chemical class 0.000 claims description 4
- 239000000460 chlorine Substances 0.000 claims description 3
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 claims description 2
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 2
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 2
- 229910052794 bromium Inorganic materials 0.000 claims description 2
- 229910052801 chlorine Inorganic materials 0.000 claims description 2
- 229910052740 iodine Inorganic materials 0.000 claims description 2
- 239000011630 iodine Substances 0.000 claims description 2
- 125000001064 morpholinomethyl group Chemical group [H]C([H])(*)N1C([H])([H])C([H])([H])OC([H])([H])C1([H])[H] 0.000 claims description 2
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 1
- 150000002431 hydrogen Chemical class 0.000 claims 1
- 239000004480 active ingredient Substances 0.000 description 90
- 241000196324 Embryophyta Species 0.000 description 36
- 206010061217 Infestation Diseases 0.000 description 23
- 238000012360 testing method Methods 0.000 description 20
- 239000000203 mixture Substances 0.000 description 14
- 239000002904 solvent Substances 0.000 description 13
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 13
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 12
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 12
- 230000012010 growth Effects 0.000 description 12
- 241000221785 Erysiphales Species 0.000 description 11
- 239000007921 spray Substances 0.000 description 11
- 239000003795 chemical substances by application Substances 0.000 description 10
- 239000007788 liquid Substances 0.000 description 10
- 241000209219 Hordeum Species 0.000 description 9
- 241000220225 Malus Species 0.000 description 9
- 201000010099 disease Diseases 0.000 description 9
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 9
- 239000000758 substrate Substances 0.000 description 9
- -1 2-Ethylphenoxymethyl Chemical group 0.000 description 8
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 8
- 235000007340 Hordeum vulgare Nutrition 0.000 description 7
- 230000000694 effects Effects 0.000 description 7
- 239000003995 emulsifying agent Substances 0.000 description 7
- 208000015181 infectious disease Diseases 0.000 description 7
- 238000002360 preparation method Methods 0.000 description 7
- 239000002689 soil Substances 0.000 description 7
- 125000002877 alkyl aryl group Chemical group 0.000 description 6
- 150000001875 compounds Chemical class 0.000 description 6
- 239000012141 concentrate Substances 0.000 description 6
- 229920000151 polyglycol Polymers 0.000 description 6
- 239000010695 polyglycol Substances 0.000 description 6
- 229920001817 Agar Polymers 0.000 description 5
- 235000021186 dishes Nutrition 0.000 description 5
- 238000009472 formulation Methods 0.000 description 5
- 238000011081 inoculation Methods 0.000 description 5
- 230000001681 protective effect Effects 0.000 description 5
- 239000011877 solvent mixture Substances 0.000 description 5
- 240000008067 Cucumis sativus Species 0.000 description 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
- 239000000654 additive Substances 0.000 description 4
- 239000008272 agar Substances 0.000 description 4
- 235000010419 agar Nutrition 0.000 description 4
- 239000001963 growth medium Substances 0.000 description 4
- 239000002609 medium Substances 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- 239000000843 powder Substances 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- NPZDCTUDQYGYQD-UHFFFAOYSA-N 1-tritylimidazole Chemical class C1=NC=CN1C(C=1C=CC=CC=1)(C=1C=CC=CC=1)C1=CC=CC=C1 NPZDCTUDQYGYQD-UHFFFAOYSA-N 0.000 description 3
- 235000001674 Agaricus brunnescens Nutrition 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- 241000221787 Erysiphe Species 0.000 description 3
- 206010017533 Fungal infection Diseases 0.000 description 3
- 241000223221 Fusarium oxysporum Species 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 241001617088 Thanatephorus sasakii Species 0.000 description 3
- 239000013543 active substance Substances 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 239000002270 dispersing agent Substances 0.000 description 3
- 230000002538 fungal effect Effects 0.000 description 3
- 208000024386 fungal infectious disease Diseases 0.000 description 3
- 239000002054 inoculum Substances 0.000 description 3
- 235000015097 nutrients Nutrition 0.000 description 3
- 150000002902 organometallic compounds Chemical class 0.000 description 3
- 238000005554 pickling Methods 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- 239000000725 suspension Substances 0.000 description 3
- 239000000454 talc Substances 0.000 description 3
- 229910052623 talc Inorganic materials 0.000 description 3
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
- 239000004606 Fillers/Extenders Substances 0.000 description 2
- 241000489964 Fusicladium Species 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- 240000001931 Ludwigia octovalvis Species 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- MZRVEZGGRBJDDB-UHFFFAOYSA-N N-Butyllithium Chemical compound [Li]CCCC MZRVEZGGRBJDDB-UHFFFAOYSA-N 0.000 description 2
- GXCLVBGFBYZDAG-UHFFFAOYSA-N N-[2-(1H-indol-3-yl)ethyl]-N-methylprop-2-en-1-amine Chemical compound CN(CCC1=CNC2=C1C=CC=C2)CC=C GXCLVBGFBYZDAG-UHFFFAOYSA-N 0.000 description 2
- 240000007594 Oryza sativa Species 0.000 description 2
- 208000012868 Overgrowth Diseases 0.000 description 2
- 241000896242 Podosphaera Species 0.000 description 2
- 241001337928 Podosphaera leucotricha Species 0.000 description 2
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 2
- 241000228454 Pyrenophora graminea Species 0.000 description 2
- KAESVJOAVNADME-UHFFFAOYSA-N Pyrrole Chemical compound C=1C=CNC=1 KAESVJOAVNADME-UHFFFAOYSA-N 0.000 description 2
- 206010039509 Scab Diseases 0.000 description 2
- RAHZWNYVWXNFOC-UHFFFAOYSA-N Sulphur dioxide Chemical compound O=S=O RAHZWNYVWXNFOC-UHFFFAOYSA-N 0.000 description 2
- 230000000895 acaricidal effect Effects 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 230000000844 anti-bacterial effect Effects 0.000 description 2
- 229940098396 barley grain Drugs 0.000 description 2
- ZCCIPPOKBCJFDN-UHFFFAOYSA-N calcium nitrate Chemical compound [Ca+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O ZCCIPPOKBCJFDN-UHFFFAOYSA-N 0.000 description 2
- 239000007795 chemical reaction product Substances 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 238000010410 dusting Methods 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- 239000000417 fungicide Substances 0.000 description 2
- 230000035784 germination Effects 0.000 description 2
- 239000008187 granular material Substances 0.000 description 2
- 125000004435 hydrogen atom Chemical class [H]* 0.000 description 2
- 239000012442 inert solvent Substances 0.000 description 2
- 230000002401 inhibitory effect Effects 0.000 description 2
- 230000017066 negative regulation of growth Effects 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- 125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 description 2
- 239000006072 paste Substances 0.000 description 2
- 244000052769 pathogen Species 0.000 description 2
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
- 239000002243 precursor Substances 0.000 description 2
- 238000005507 spraying Methods 0.000 description 2
- 208000024891 symptom Diseases 0.000 description 2
- NZZRRHNSHYCKJA-UHFFFAOYSA-N 2-(1h-pyrrol-2-ylsulfinyl)-1h-pyrrole Chemical compound C=1C=CNC=1S(=O)C1=CC=CN1 NZZRRHNSHYCKJA-UHFFFAOYSA-N 0.000 description 1
- UHPMCKVQTMMPCG-UHFFFAOYSA-N 5,8-dihydroxy-2-methoxy-6-methyl-7-(2-oxopropyl)naphthalene-1,4-dione Chemical compound CC1=C(CC(C)=O)C(O)=C2C(=O)C(OC)=CC(=O)C2=C1O UHPMCKVQTMMPCG-UHFFFAOYSA-N 0.000 description 1
- 241000238876 Acari Species 0.000 description 1
- 241000223600 Alternaria Species 0.000 description 1
- 241000235349 Ascomycota Species 0.000 description 1
- 241000221198 Basidiomycota Species 0.000 description 1
- 241001450781 Bipolaris oryzae Species 0.000 description 1
- 241001480061 Blumeria graminis Species 0.000 description 1
- 241000123650 Botrytis cinerea Species 0.000 description 1
- 241001529717 Corticium <basidiomycota> Species 0.000 description 1
- 235000010799 Cucumis sativus var sativus Nutrition 0.000 description 1
- 241000223218 Fusarium Species 0.000 description 1
- 241000223194 Fusarium culmorum Species 0.000 description 1
- 241000879841 Fusarium oxysporum f. cubense Species 0.000 description 1
- 241000427940 Fusarium solani Species 0.000 description 1
- 241000206672 Gelidium Species 0.000 description 1
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 1
- 241000896218 Golovinomyces orontii Species 0.000 description 1
- 241000238631 Hexapoda 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
- 241001465754 Metazoa Species 0.000 description 1
- 241001459558 Monographella nivalis Species 0.000 description 1
- 241001329956 Nothopassalora personata Species 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 235000007164 Oryza sativa Nutrition 0.000 description 1
- 239000001888 Peptone Substances 0.000 description 1
- 108010080698 Peptones Proteins 0.000 description 1
- 241000222831 Phialophora <Chaetothyriales> Species 0.000 description 1
- 241000308483 Phialophora cinerescens Species 0.000 description 1
- 241001149949 Phytophthora cactorum Species 0.000 description 1
- 241001281803 Plasmopara viticola Species 0.000 description 1
- 241000184297 Pseudocercospora musae Species 0.000 description 1
- 235000014443 Pyrus communis Nutrition 0.000 description 1
- 206010037888 Rash pustular Diseases 0.000 description 1
- 241000813090 Rhizoctonia solani Species 0.000 description 1
- 241000221696 Sclerotinia sclerotiorum Species 0.000 description 1
- 244000061456 Solanum tuberosum Species 0.000 description 1
- 235000002595 Solanum tuberosum Nutrition 0.000 description 1
- 241000592344 Spermatophyta Species 0.000 description 1
- 241000865903 Thielaviopsis Species 0.000 description 1
- 241000561282 Thielaviopsis basicola Species 0.000 description 1
- 241000722093 Tilletia caries Species 0.000 description 1
- 241000287436 Turdus merula Species 0.000 description 1
- 241000317942 Venturia <ichneumonid wasp> Species 0.000 description 1
- 241000228452 Venturia inaequalis Species 0.000 description 1
- 241001123669 Verticillium albo-atrum Species 0.000 description 1
- 239000000642 acaricide Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 230000002353 algacidal effect Effects 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 150000008055 alkyl aryl sulfonates Chemical class 0.000 description 1
- 150000001350 alkyl halides Chemical class 0.000 description 1
- 229940045714 alkyl sulfonate alkylating agent Drugs 0.000 description 1
- 150000008052 alkyl sulfonates Chemical class 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 230000001857 anti-mycotic effect Effects 0.000 description 1
- 239000002543 antimycotic Substances 0.000 description 1
- 239000007900 aqueous suspension Substances 0.000 description 1
- 235000019568 aromas Nutrition 0.000 description 1
- 239000003899 bactericide agent Substances 0.000 description 1
- 150000007514 bases Chemical class 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000011203 carbon fibre reinforced carbon Substances 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 239000012876 carrier material Substances 0.000 description 1
- 239000013043 chemical agent Substances 0.000 description 1
- 150000008422 chlorobenzenes Chemical class 0.000 description 1
- 239000008121 dextrose Substances 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 231100000676 disease causative agent Toxicity 0.000 description 1
- BNIILDVGGAEEIG-UHFFFAOYSA-L disodium hydrogen phosphate Chemical compound [Na+].[Na+].OP([O-])([O-])=O BNIILDVGGAEEIG-UHFFFAOYSA-L 0.000 description 1
- 229910000397 disodium phosphate Inorganic materials 0.000 description 1
- 235000019800 disodium phosphate Nutrition 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 235000013399 edible fruits Nutrition 0.000 description 1
- 239000004495 emulsifiable concentrate Substances 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 239000003337 fertilizer Substances 0.000 description 1
- 235000013312 flour Nutrition 0.000 description 1
- 230000000855 fungicidal effect Effects 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 230000009036 growth inhibition Effects 0.000 description 1
- 239000003630 growth substance Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000004009 herbicide Substances 0.000 description 1
- 125000000623 heterocyclic group Chemical group 0.000 description 1
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 1
- 229910000041 hydrogen chloride Inorganic materials 0.000 description 1
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Substances C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 description 1
- 238000011534 incubation Methods 0.000 description 1
- 230000000749 insecticidal effect Effects 0.000 description 1
- 239000002917 insecticide Substances 0.000 description 1
- 238000002955 isolation Methods 0.000 description 1
- 229920005610 lignin Polymers 0.000 description 1
- 238000009630 liquid culture Methods 0.000 description 1
- 231100000053 low toxicity Toxicity 0.000 description 1
- 125000000040 m-tolyl group Chemical group [H]C1=C([H])C(*)=C([H])C(=C1[H])C([H])([H])[H] 0.000 description 1
- CCERQOYLJJULMD-UHFFFAOYSA-M magnesium;carbanide;chloride Chemical compound [CH3-].[Mg+2].[Cl-] CCERQOYLJJULMD-UHFFFAOYSA-M 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 235000010981 methylcellulose Nutrition 0.000 description 1
- 230000003641 microbiacidal effect Effects 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000005645 nematicide Substances 0.000 description 1
- 230000003071 parasitic effect Effects 0.000 description 1
- 230000001717 pathogenic effect Effects 0.000 description 1
- 235000019319 peptone Nutrition 0.000 description 1
- 239000000575 pesticide Substances 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 230000003032 phytopathogenic effect Effects 0.000 description 1
- 230000008635 plant growth Effects 0.000 description 1
- 239000005648 plant growth regulator Substances 0.000 description 1
- 239000002798 polar solvent Substances 0.000 description 1
- 239000000256 polyoxyethylene sorbitan monolaurate Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- 239000001965 potato dextrose agar Substances 0.000 description 1
- 230000001376 precipitating effect Effects 0.000 description 1
- 230000003449 preventive effect Effects 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 208000029561 pustule Diseases 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 235000009566 rice Nutrition 0.000 description 1
- 239000011435 rock Substances 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 230000000391 smoking effect Effects 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 239000001488 sodium phosphate Substances 0.000 description 1
- 238000007711 solidification Methods 0.000 description 1
- 230000008023 solidification Effects 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 239000004575 stone Substances 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-L sulfite Chemical compound [O-]S([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-L 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 230000009885 systemic effect Effects 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 239000002699 waste material 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
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
- A01N43/50—1,3-Diazoles; Hydrogenated 1,3-diazoles
-
- 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
- C07D233/56—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 only hydrogen atoms or radicals containing only hydrogen and carbon atoms, attached to ring carbon atoms
-
- 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
- C07D233/64—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 substituted hydrocarbon radicals attached to ring carbon atoms, e.g. histidine
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
- C07D249/02—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
- C07D249/08—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- 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)
Priority Applications (24)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE2128700A DE2128700C2 (de) | 1971-06-09 | 1971-06-09 | Fungitoxische Mittel |
| US00257365A US3832466A (en) | 1971-06-09 | 1972-05-26 | 3-azolylpropyne fungicidal agents |
| EG216/72*UA EG10528A (en) | 1971-06-09 | 1972-05-29 | Compound of 3-azolyl propynes used as fungicides and bactericides |
| CS3792A CS170188B2 (en, 2012) | 1971-06-09 | 1972-06-01 | |
| IL39617A IL39617A (en) | 1971-06-09 | 1972-06-06 | Fungitoxic and bactericidal compositions containing 3-imidazolylpropynes and their use |
| TR18524A TR18524A (tr) | 1971-06-09 | 1972-06-06 | Fungisoksik maddeler |
| AT489772A AT316209B (de) | 1971-06-09 | 1972-06-07 | Fungizide und bakterizide Mittel |
| BR3666/72A BR7203666D0 (pt) | 1971-06-09 | 1972-06-07 | Composicao fungicida e bactericida |
| IT25369/72A IT961223B (it) | 1971-06-09 | 1972-06-07 | Agenti fungitossici |
| DD163511A DD103135A5 (en, 2012) | 1971-06-09 | 1972-06-07 | |
| CH845372A CH531833A (de) | 1971-06-09 | 1972-06-07 | Verwendung von 3-Azolylpropinen zur Bekämpfung von Fungi und Bakterien |
| ZA723937A ZA723937B (en) | 1971-06-09 | 1972-06-08 | Fungitoxic and bactericidal agents |
| PL1972155893A PL84075B1 (en, 2012) | 1971-06-09 | 1972-06-08 | |
| GB2674672A GB1365634A (en) | 1971-06-09 | 1972-06-08 | Fungitoxic and bactericidal agents |
| JP47056536A JPS5751802B1 (en, 2012) | 1971-06-09 | 1972-06-08 | |
| NLAANVRAGE7207797,A NL176130C (nl) | 1971-06-09 | 1972-06-08 | Werkwijze voor het bereiden van fungicide en bactericide preparaten. |
| DK287472AA DK132054C (da) | 1971-06-09 | 1972-06-08 | Fungicidt og baktericidt middel. |
| CA144,190A CA972287A (en) | 1971-06-09 | 1972-06-08 | Fungitoxic and bactericidal agents |
| ES403651A ES403651A1 (es) | 1971-06-09 | 1972-06-08 | Procedimiento para preparar composiciones fungicidas y bac-tericidas. |
| IE796/72A IE36407B1 (en) | 1971-06-09 | 1972-06-08 | Fungitoxic and bactericidal agents |
| BE784587A BE784587A (fr) | 1971-06-09 | 1972-06-08 | Nouvelles compositions fongitoxiques |
| HUBA2752A HU164708B (en, 2012) | 1971-06-09 | 1972-06-09 | |
| FR7220825A FR2140622B1 (en, 2012) | 1971-06-09 | 1972-06-09 | |
| MY51/75A MY7500051A (en) | 1971-06-09 | 1975-12-30 | Fungitoxic and bacteridical agents |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE2128700A DE2128700C2 (de) | 1971-06-09 | 1971-06-09 | Fungitoxische Mittel |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| DE2128700A1 DE2128700A1 (de) | 1973-01-04 |
| DE2128700C2 true DE2128700C2 (de) | 1985-04-25 |
Family
ID=5810336
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE2128700A Expired DE2128700C2 (de) | 1971-06-09 | 1971-06-09 | Fungitoxische Mittel |
Country Status (24)
| Country | Link |
|---|---|
| US (1) | US3832466A (en, 2012) |
| JP (1) | JPS5751802B1 (en, 2012) |
| AT (1) | AT316209B (en, 2012) |
| BE (1) | BE784587A (en, 2012) |
| BR (1) | BR7203666D0 (en, 2012) |
| CA (1) | CA972287A (en, 2012) |
| CH (1) | CH531833A (en, 2012) |
| CS (1) | CS170188B2 (en, 2012) |
| DD (1) | DD103135A5 (en, 2012) |
| DE (1) | DE2128700C2 (en, 2012) |
| DK (1) | DK132054C (en, 2012) |
| EG (1) | EG10528A (en, 2012) |
| ES (1) | ES403651A1 (en, 2012) |
| FR (1) | FR2140622B1 (en, 2012) |
| GB (1) | GB1365634A (en, 2012) |
| HU (1) | HU164708B (en, 2012) |
| IE (1) | IE36407B1 (en, 2012) |
| IL (1) | IL39617A (en, 2012) |
| IT (1) | IT961223B (en, 2012) |
| MY (1) | MY7500051A (en, 2012) |
| NL (1) | NL176130C (en, 2012) |
| PL (1) | PL84075B1 (en, 2012) |
| TR (1) | TR18524A (en, 2012) |
| ZA (1) | ZA723937B (en, 2012) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2560510C2 (en, 2012) * | 1975-11-26 | 1989-02-16 | Bayer Ag, 5090 Leverkusen, De | |
| DE3307909A1 (de) * | 1983-03-05 | 1984-09-06 | Bayer Ag, 5090 Leverkusen | Fungizides mittel, verfahren zu dessen herstellung, sowie dessen verwendung |
| JPH03149404A (ja) * | 1989-10-31 | 1991-06-26 | Iseki & Co Ltd | 油圧装置 |
| JPH0385773U (en, 2012) * | 1989-12-14 | 1991-08-29 | ||
| JP2001039954A (ja) * | 1999-05-24 | 2001-02-13 | Tomono Agrica Co Ltd | ヘテロ環誘導体 |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1091103B (de) * | 1957-12-18 | 1960-10-20 | Basf Ag | Verfahren zur Herstellung von einen oder zwei stickstoffhaltige Reste und eine Kohlenstoff-Kohlenstoff-Dreifachbindung enthaltenden Verbindungen |
| US2971006A (en) * | 1959-12-11 | 1961-02-07 | Gen Aniline & Film Corp | 1-(-alkyl or -hydroxyalkyl)-1-(2-propynyl)-2-alkylimidazolinium halides |
| US3321366A (en) * | 1965-11-15 | 1967-05-23 | Dow Chemical Co | Fungicidal methods and compositions |
| US3479367A (en) * | 1966-10-03 | 1969-11-18 | Pfizer & Co C | 1-substituted-2-alkyl-5-nitroimidazoles |
| CH509040A (de) * | 1968-10-17 | 1971-06-30 | Ciba Geigy Ag | Schädlingsbekämpfungsmittel |
| BR6915465D0 (pt) * | 1969-03-07 | 1973-01-04 | Bayer Ag | Processo para preparar n-benzimidazois substituidos na posicao alfa por heterociclos penta-membrados com atividade antimicotica |
-
1971
- 1971-06-09 DE DE2128700A patent/DE2128700C2/de not_active Expired
-
1972
- 1972-05-26 US US00257365A patent/US3832466A/en not_active Expired - Lifetime
- 1972-05-29 EG EG216/72*UA patent/EG10528A/xx active
- 1972-06-01 CS CS3792A patent/CS170188B2/cs unknown
- 1972-06-06 TR TR18524A patent/TR18524A/xx unknown
- 1972-06-06 IL IL39617A patent/IL39617A/xx unknown
- 1972-06-07 IT IT25369/72A patent/IT961223B/it active
- 1972-06-07 CH CH845372A patent/CH531833A/de not_active IP Right Cessation
- 1972-06-07 AT AT489772A patent/AT316209B/de not_active IP Right Cessation
- 1972-06-07 DD DD163511A patent/DD103135A5/xx unknown
- 1972-06-07 BR BR3666/72A patent/BR7203666D0/pt unknown
- 1972-06-08 DK DK287472AA patent/DK132054C/da not_active IP Right Cessation
- 1972-06-08 ZA ZA723937A patent/ZA723937B/xx unknown
- 1972-06-08 PL PL1972155893A patent/PL84075B1/pl unknown
- 1972-06-08 NL NLAANVRAGE7207797,A patent/NL176130C/xx not_active IP Right Cessation
- 1972-06-08 GB GB2674672A patent/GB1365634A/en not_active Expired
- 1972-06-08 ES ES403651A patent/ES403651A1/es not_active Expired
- 1972-06-08 CA CA144,190A patent/CA972287A/en not_active Expired
- 1972-06-08 BE BE784587A patent/BE784587A/xx not_active IP Right Cessation
- 1972-06-08 IE IE796/72A patent/IE36407B1/xx unknown
- 1972-06-08 JP JP47056536A patent/JPS5751802B1/ja active Pending
- 1972-06-09 HU HUBA2752A patent/HU164708B/hu unknown
- 1972-06-09 FR FR7220825A patent/FR2140622B1/fr not_active Expired
-
1975
- 1975-12-30 MY MY51/75A patent/MY7500051A/xx unknown
Also Published As
| Publication number | Publication date |
|---|---|
| US3832466A (en) | 1974-08-27 |
| IT961223B (it) | 1973-12-10 |
| DD103135A5 (en, 2012) | 1974-01-12 |
| FR2140622B1 (en, 2012) | 1977-12-30 |
| MY7500051A (en) | 1975-12-31 |
| NL176130B (nl) | 1984-10-01 |
| CA972287A (en) | 1975-08-05 |
| ZA723937B (en) | 1973-03-28 |
| NL7207797A (en, 2012) | 1972-12-12 |
| IL39617A (en) | 1975-02-10 |
| IE36407L (en) | 1972-12-09 |
| GB1365634A (en) | 1974-09-04 |
| TR18524A (tr) | 1977-03-04 |
| HU164708B (en, 2012) | 1974-04-11 |
| EG10528A (en) | 1976-02-29 |
| BR7203666D0 (pt) | 1973-05-31 |
| FR2140622A1 (en, 2012) | 1973-01-19 |
| JPS5751802B1 (en, 2012) | 1982-11-04 |
| DE2128700A1 (de) | 1973-01-04 |
| DK132054B (en, 2012) | 1975-10-20 |
| PL84075B1 (en, 2012) | 1976-02-28 |
| IL39617A0 (en) | 1972-08-30 |
| AT316209B (de) | 1974-06-25 |
| NL176130C (nl) | 1985-03-01 |
| CS170188B2 (en, 2012) | 1976-08-27 |
| ES403651A1 (es) | 1975-05-01 |
| IE36407B1 (en) | 1976-10-27 |
| DK132054C (da) | 1977-06-20 |
| CH531833A (de) | 1972-12-31 |
| BE784587A (fr) | 1972-12-08 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| OD | Request for examination | ||
| D2 | Grant after examination | ||
| 8364 | No opposition during term of opposition | ||
| 8339 | Ceased/non-payment of the annual fee |