DE2535332A1 - Fungizide mittel - Google Patents
Fungizide mittelInfo
- Publication number
- DE2535332A1 DE2535332A1 DE19752535332 DE2535332A DE2535332A1 DE 2535332 A1 DE2535332 A1 DE 2535332A1 DE 19752535332 DE19752535332 DE 19752535332 DE 2535332 A DE2535332 A DE 2535332A DE 2535332 A1 DE2535332 A1 DE 2535332A1
- Authority
- DE
- Germany
- Prior art keywords
- carbon atoms
- seed
- gibberellic acid
- combination
- gibberellins
- 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.)
- Pending
Links
- IXORZMNAPKEEDV-OBDJNFEBSA-N gibberellin A3 Chemical class C([C@@]1(O)C(=C)C[C@@]2(C1)[C@H]1C(O)=O)C[C@H]2[C@]2(C=C[C@@H]3O)[C@H]1[C@]3(C)C(=O)O2 IXORZMNAPKEEDV-OBDJNFEBSA-N 0.000 claims description 39
- 229930191978 Gibberellin Natural products 0.000 claims description 16
- 239000003448 gibberellin Substances 0.000 claims description 16
- 239000000203 mixture Substances 0.000 claims description 15
- 125000004432 carbon atom Chemical group C* 0.000 claims description 10
- 150000003839 salts Chemical class 0.000 claims description 8
- NSPMIYGKQJPBQR-UHFFFAOYSA-N 4H-1,2,4-triazole Chemical class C=1N=CNN=1 NSPMIYGKQJPBQR-UHFFFAOYSA-N 0.000 claims description 7
- 241000233866 Fungi Species 0.000 claims description 7
- 230000000855 fungicidal effect Effects 0.000 claims description 7
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 7
- 125000000217 alkyl group Chemical group 0.000 claims description 6
- 239000000417 fungicide Substances 0.000 claims description 6
- 238000002360 preparation method Methods 0.000 claims description 5
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims description 4
- 239000004606 Fillers/Extenders Substances 0.000 claims description 4
- 239000003513 alkali Substances 0.000 claims description 4
- 229910052736 halogen Inorganic materials 0.000 claims description 3
- 150000002367 halogens Chemical class 0.000 claims description 3
- 229910052739 hydrogen Inorganic materials 0.000 claims description 3
- 239000001257 hydrogen Substances 0.000 claims description 3
- 150000007522 mineralic acids Chemical class 0.000 claims description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 2
- 125000003545 alkoxy group Chemical group 0.000 claims description 2
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 2
- 125000000896 monocarboxylic acid group Chemical group 0.000 claims description 2
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 2
- 125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 claims description 2
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 2
- 238000000034 method Methods 0.000 claims 2
- 239000004094 surface-active agent Substances 0.000 claims 1
- IXORZMNAPKEEDV-UHFFFAOYSA-N gibberellic acid GA3 Natural products OC(=O)C1C2(C3)CC(=C)C3(O)CCC2C2(C=CC3O)C1C3(C)C(=O)O2 IXORZMNAPKEEDV-UHFFFAOYSA-N 0.000 description 35
- 239000005980 Gibberellic acid Substances 0.000 description 29
- 239000004480 active ingredient Substances 0.000 description 26
- 238000007792 addition Methods 0.000 description 19
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 19
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 15
- 238000005554 pickling Methods 0.000 description 15
- 238000011282 treatment Methods 0.000 description 14
- 239000003795 chemical substances by application Substances 0.000 description 13
- -1 ethylene bis-nitrourethanes Chemical class 0.000 description 12
- 239000002689 soil Substances 0.000 description 12
- 239000006004 Quartz sand Substances 0.000 description 11
- 241000196324 Embryophyta Species 0.000 description 10
- FGIUAXJPYTZDNR-UHFFFAOYSA-N potassium nitrate Chemical compound [K+].[O-][N+]([O-])=O FGIUAXJPYTZDNR-UHFFFAOYSA-N 0.000 description 10
- 239000000654 additive Substances 0.000 description 9
- 239000000843 powder Substances 0.000 description 8
- 238000011156 evaluation Methods 0.000 description 7
- 230000012010 growth Effects 0.000 description 7
- 239000007788 liquid Substances 0.000 description 7
- 239000002253 acid Substances 0.000 description 6
- 230000005764 inhibitory process Effects 0.000 description 6
- 239000000758 substrate Substances 0.000 description 6
- 241000221785 Erysiphales Species 0.000 description 5
- 206010061217 Infestation Diseases 0.000 description 5
- 241000209140 Triticum Species 0.000 description 5
- 235000021307 Triticum Nutrition 0.000 description 5
- 238000009472 formulation Methods 0.000 description 5
- 229910000402 monopotassium phosphate Inorganic materials 0.000 description 5
- 235000019796 monopotassium phosphate Nutrition 0.000 description 5
- PJNZPQUBCPKICU-UHFFFAOYSA-N phosphoric acid;potassium Chemical compound [K].OP(O)(O)=O PJNZPQUBCPKICU-UHFFFAOYSA-N 0.000 description 5
- 239000004323 potassium nitrate Substances 0.000 description 5
- 235000010333 potassium nitrate Nutrition 0.000 description 5
- 238000009331 sowing Methods 0.000 description 5
- ZNQVEEAIQZEUHB-UHFFFAOYSA-N 2-ethoxyethanol Chemical compound CCOCCO ZNQVEEAIQZEUHB-UHFFFAOYSA-N 0.000 description 4
- 241000209219 Hordeum Species 0.000 description 4
- RSPISYXLHRIGJD-UHFFFAOYSA-N OOOO Chemical compound OOOO RSPISYXLHRIGJD-UHFFFAOYSA-N 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 238000002474 experimental method Methods 0.000 description 4
- 230000002401 inhibitory effect Effects 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
- 241000894006 Bacteria Species 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- 235000007340 Hordeum vulgare Nutrition 0.000 description 3
- PVNIIMVLHYAWGP-UHFFFAOYSA-N Niacin Chemical compound OC(=O)C1=CC=CN=C1 PVNIIMVLHYAWGP-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 238000009825 accumulation Methods 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
- 239000003995 emulsifying agent Substances 0.000 description 3
- 239000003630 growth substance Substances 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- 229940042055 systemic antimycotics triazole derivative Drugs 0.000 description 3
- 239000000454 talc Substances 0.000 description 3
- 229910052623 talc Inorganic materials 0.000 description 3
- 241001480061 Blumeria graminis Species 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
- 240000002024 Gossypium herbaceum Species 0.000 description 2
- 235000004341 Gossypium herbaceum Nutrition 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 2
- WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical compound [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 description 2
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 235000013339 cereals Nutrition 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
- 230000006735 deficit Effects 0.000 description 2
- 239000002270 dispersing agent Substances 0.000 description 2
- 239000000834 fixative Substances 0.000 description 2
- 235000013312 flour Nutrition 0.000 description 2
- 230000002464 fungitoxic effect Effects 0.000 description 2
- 230000009036 growth inhibition Effects 0.000 description 2
- 208000015181 infectious disease Diseases 0.000 description 2
- 239000003921 oil Substances 0.000 description 2
- 239000006072 paste Substances 0.000 description 2
- 230000008635 plant growth Effects 0.000 description 2
- 239000004576 sand Substances 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 239000011877 solvent mixture Substances 0.000 description 2
- 238000005507 spraying Methods 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 239000000725 suspension Substances 0.000 description 2
- 230000009885 systemic effect Effects 0.000 description 2
- JNDNSKMAFGPBFU-BEAPCOKYSA-N (1s,2r,5r,8s)-8-(hydroxymethyl)-5,6-dimethyl-2-propan-2-ylbicyclo[3.2.1]oct-6-ene-7-carbaldehyde Chemical compound CC(C)[C@H]1CC[C@@]2(C)C(C)=C(C=O)[C@@H]1[C@@H]2CO JNDNSKMAFGPBFU-BEAPCOKYSA-N 0.000 description 1
- VRNXAQRALVPTGJ-CIUDSAMLSA-N (2s,3s,4s)-4-methyl-5-oxo-2-pentyloxolane-3-carboxylic acid Chemical compound CCCCC[C@@H]1OC(=O)[C@@H](C)[C@@H]1C(O)=O VRNXAQRALVPTGJ-CIUDSAMLSA-N 0.000 description 1
- KFBNKQBAHPSQHK-UHFFFAOYSA-N 1-(2,4-dichlorophenoxy)-3,3-dimethyl-1-(1,2,4-triazol-1-yl)butan-2-one Chemical compound C1=NC=NN1C(C(=O)C(C)(C)C)OC1=CC=C(Cl)C=C1Cl KFBNKQBAHPSQHK-UHFFFAOYSA-N 0.000 description 1
- WURBVZBTWMNKQT-UHFFFAOYSA-N 1-(4-chlorophenoxy)-3,3-dimethyl-1-(1,2,4-triazol-1-yl)butan-2-one Chemical compound C1=NC=NN1C(C(=O)C(C)(C)C)OC1=CC=C(Cl)C=C1 WURBVZBTWMNKQT-UHFFFAOYSA-N 0.000 description 1
- DRPSWDKWLOPHPG-UHFFFAOYSA-N 1-(triazol-1-yl)butan-2-one Chemical compound CCC(=O)CN1C=CN=N1 DRPSWDKWLOPHPG-UHFFFAOYSA-N 0.000 description 1
- OBJSERXHTZNJCR-UHFFFAOYSA-N 2-methoxyethylmercury(1+);trihydroxy(oxido)silane Chemical compound COCC[Hg+].O[Si](O)(O)[O-] OBJSERXHTZNJCR-UHFFFAOYSA-N 0.000 description 1
- 241000235349 Ascomycota Species 0.000 description 1
- 241000221198 Basidiomycota Species 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 241000760356 Chytridiomycetes Species 0.000 description 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
- 241000221787 Erysiphe Species 0.000 description 1
- AHRZQDHJIUYION-UHFFFAOYSA-N Helminthosporol Natural products CC(C)C1CCC2C=C(C=O)C1C2CO AHRZQDHJIUYION-UHFFFAOYSA-N 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
- IXORZMNAPKEEDV-SNTJWBGVSA-N LSM-6641 Chemical compound C([C@@]1(O)C(=C)C[C@@]2(C1)[C@H]1C(O)=O)C[C@H]2[C@]2(C=C[C@@H]3O)[C@H]1[C@@]3(C)C(=O)O2 IXORZMNAPKEEDV-SNTJWBGVSA-N 0.000 description 1
- 240000001931 Ludwigia octovalvis Species 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 1
- UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 241000233654 Oomycetes Species 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- VRNXAQRALVPTGJ-UHFFFAOYSA-N Phaseolinic acid Natural products CCCCCC1OC(=O)C(C)C1C(O)=O VRNXAQRALVPTGJ-UHFFFAOYSA-N 0.000 description 1
- 241001503460 Plasmodiophorida Species 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 206010037888 Rash pustular Diseases 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical class ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- 241000607479 Yersinia pestis Species 0.000 description 1
- 230000000895 acaricidal effect Effects 0.000 description 1
- 239000000642 acaricide Substances 0.000 description 1
- 239000013543 active substance Substances 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 125000002877 alkyl aryl group Chemical group 0.000 description 1
- 150000008055 alkyl aryl sulfonates Chemical class 0.000 description 1
- 150000008051 alkyl sulfates 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
- 239000007900 aqueous suspension Substances 0.000 description 1
- 229960000892 attapulgite Drugs 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 1
- 150000001805 chlorine compounds Chemical class 0.000 description 1
- 150000008422 chlorobenzenes Chemical class 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 230000000295 complement effect Effects 0.000 description 1
- 230000003111 delayed effect Effects 0.000 description 1
- GUJOJGAPFQRJSV-UHFFFAOYSA-N dialuminum;dioxosilane;oxygen(2-);hydrate Chemical compound O.[O-2].[O-2].[O-2].[Al+3].[Al+3].O=[Si]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O GUJOJGAPFQRJSV-UHFFFAOYSA-N 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 201000010099 disease Diseases 0.000 description 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 1
- 238000010410 dusting Methods 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 230000003631 expected effect Effects 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 239000003337 fertilizer Substances 0.000 description 1
- 239000000446 fuel Substances 0.000 description 1
- 230000002538 fungal effect Effects 0.000 description 1
- 231100000162 fungitoxic Toxicity 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 230000035784 germination Effects 0.000 description 1
- JLJLRLWOEMWYQK-OBDJNFEBSA-N gibberellin A1 Chemical compound C([C@@]1(O)C(=C)C[C@@]2(C1)[C@H]1C(O)=O)C[C@H]2[C@@]2(OC3=O)[C@H]1[C@@]3(C)[C@@H](O)CC2 JLJLRLWOEMWYQK-OBDJNFEBSA-N 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 239000003966 growth inhibitor Substances 0.000 description 1
- 150000008282 halocarbons Chemical class 0.000 description 1
- 150000002431 hydrogen Chemical class 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 239000002917 insecticide Substances 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 229920005610 lignin Polymers 0.000 description 1
- 231100000053 low toxicity Toxicity 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 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
- 239000011707 mineral Substances 0.000 description 1
- 230000003020 moisturizing effect Effects 0.000 description 1
- 229910052901 montmorillonite Inorganic materials 0.000 description 1
- 150000002823 nitrates Chemical class 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
- 229910052625 palygorskite Inorganic materials 0.000 description 1
- 230000003071 parasitic effect Effects 0.000 description 1
- 244000052769 pathogen Species 0.000 description 1
- 239000000575 pesticide Substances 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 235000021317 phosphate Nutrition 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 230000035479 physiological effects, processes and functions Effects 0.000 description 1
- 230000003032 phytopathogenic effect Effects 0.000 description 1
- 230000000885 phytotoxic effect Effects 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 239000002798 polar solvent Substances 0.000 description 1
- 229920000151 polyglycol Polymers 0.000 description 1
- 239000010695 polyglycol Substances 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000003380 propellant Substances 0.000 description 1
- 208000029561 pustule Diseases 0.000 description 1
- 239000010453 quartz Substances 0.000 description 1
- 230000008439 repair process Effects 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
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 238000003892 spreading Methods 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-L sulfite Chemical compound [O-]S([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-L 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 230000002195 synergetic effect Effects 0.000 description 1
- 150000003852 triazoles Chemical class 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
- 230000003313 weakening effect Effects 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
- A01N43/64—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with three nitrogen atoms as the only ring hetero atoms
- A01N43/647—Triazoles; Hydrogenated triazoles
- A01N43/653—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
-
- 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
- A01N43/90—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having two or more relevant hetero rings, condensed among themselves or with a common carbocyclic ring system
-
- 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
- A01N45/00—Biocides, pest repellants or attractants, or plant growth regulators, containing compounds having three or more carbocyclic rings condensed among themselves, at least one ring not being a six-membered ring
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Priority Applications (14)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19752535332 DE2535332A1 (de) | 1975-08-07 | 1975-08-07 | Fungizide mittel |
| NO762585A NO762585L (US07582779-20090901-C00044.png) | 1975-08-07 | 1976-07-23 | |
| AU16553/76A AU1655376A (en) | 1975-08-07 | 1976-08-04 | Fungicidal agents |
| FI762251A FI762251A (US07582779-20090901-C00044.png) | 1975-08-07 | 1976-08-05 | |
| JP51092836A JPS5221330A (en) | 1975-08-07 | 1976-08-05 | Germicide |
| BE169579A BE844909A (fr) | 1975-08-07 | 1976-08-05 | Nouvelles compositions fongicides contenant des derives 1,2,4-triazoliques et des gibberellines |
| GB32669/76A GB1491856A (en) | 1975-08-07 | 1976-08-05 | Fungicidal agents |
| NL7608715A NL7608715A (nl) | 1975-08-07 | 1976-08-05 | Fungicide preparaten, werkwijze ter vervaar- diging hiervan en werkwijze ter bestrijding van fungi. |
| DD194225A DD126843A5 (US07582779-20090901-C00044.png) | 1975-08-07 | 1976-08-05 | |
| CS765126A CS189022B2 (en) | 1975-08-07 | 1976-08-05 | Fundicide,means |
| SE7608798A SE7608798L (sv) | 1975-08-07 | 1976-08-05 | Fungicit medel |
| DK355876A DK355876A (da) | 1975-08-07 | 1976-08-06 | Fungicidt middel dets fremstilling og anvendelse |
| TR18802A TR18802A (tr) | 1975-08-07 | 1976-08-06 | Fungisid terkipler |
| FR7624224A FR2320052A1 (fr) | 1975-08-07 | 1976-08-06 | Nouvelles compositions fongicides contenant des derives 1,2,4-triazoliques et des gibberellines |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19752535332 DE2535332A1 (de) | 1975-08-07 | 1975-08-07 | Fungizide mittel |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE2535332A1 true DE2535332A1 (de) | 1977-02-17 |
Family
ID=5953483
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE19752535332 Pending DE2535332A1 (de) | 1975-08-07 | 1975-08-07 | Fungizide mittel |
Country Status (14)
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0010298A1 (de) * | 1978-10-23 | 1980-04-30 | BASF Aktiengesellschaft | 1,2,4-Triazol-1-yl-Verbindungen, ihre Herstellung, Fungizide, Verfahren zur Herstellung von Fungiziden und Verfahren zur Bekämpfung von Fungi |
| EP0045016A1 (de) * | 1980-07-29 | 1982-02-03 | Bayer Ag | Substituierte Triazolylalkyl-pyridyl-ether, Verfahren zu ihrer Herstellung sowie ihre Verwendung als Fungizide |
| WO2002069715A2 (de) * | 2001-03-06 | 2002-09-12 | Bayer Cropscience Ag | Beizmittel |
| WO2007065843A2 (de) * | 2005-12-09 | 2007-06-14 | Basf Se | Verwendung von gibberellin als safener für azole zur bekämpfung von schadpilzen |
| WO2008155416A2 (en) * | 2007-06-20 | 2008-12-24 | Basf Se | Gibberellins as safeners for fungicides with phytotoxic activity |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| ZA774497B (en) | 1976-07-29 | 1978-06-28 | Ici Ltd | Processes and compositions for combating fungi |
| US4436547A (en) * | 1978-03-28 | 1984-03-13 | Staart Enterprises Ltd. | Plant technique |
| BR8008872A (pt) * | 1979-10-13 | 1981-08-25 | M Sampson | Processo para obter melhorados rendimentos de plantas |
| KR20080066997A (ko) * | 2005-11-10 | 2008-07-17 | 바스프 에스이 | 유해 진균 방제용 트리티코나졸을 위한 완화제로서의피라클로스트로빈의 용도 |
-
1975
- 1975-08-07 DE DE19752535332 patent/DE2535332A1/de active Pending
-
1976
- 1976-07-23 NO NO762585A patent/NO762585L/no unknown
- 1976-08-04 AU AU16553/76A patent/AU1655376A/en not_active Expired
- 1976-08-05 GB GB32669/76A patent/GB1491856A/en not_active Expired
- 1976-08-05 BE BE169579A patent/BE844909A/xx unknown
- 1976-08-05 NL NL7608715A patent/NL7608715A/xx not_active Application Discontinuation
- 1976-08-05 DD DD194225A patent/DD126843A5/xx unknown
- 1976-08-05 SE SE7608798A patent/SE7608798L/xx unknown
- 1976-08-05 CS CS765126A patent/CS189022B2/cs unknown
- 1976-08-05 JP JP51092836A patent/JPS5221330A/ja active Pending
- 1976-08-05 FI FI762251A patent/FI762251A/fi not_active Application Discontinuation
- 1976-08-06 FR FR7624224A patent/FR2320052A1/fr active Granted
- 1976-08-06 TR TR18802A patent/TR18802A/xx unknown
- 1976-08-06 DK DK355876A patent/DK355876A/da unknown
Cited By (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0010298A1 (de) * | 1978-10-23 | 1980-04-30 | BASF Aktiengesellschaft | 1,2,4-Triazol-1-yl-Verbindungen, ihre Herstellung, Fungizide, Verfahren zur Herstellung von Fungiziden und Verfahren zur Bekämpfung von Fungi |
| EP0045016A1 (de) * | 1980-07-29 | 1982-02-03 | Bayer Ag | Substituierte Triazolylalkyl-pyridyl-ether, Verfahren zu ihrer Herstellung sowie ihre Verwendung als Fungizide |
| US4427672A (en) | 1980-07-29 | 1984-01-24 | Bayer Aktiengesellschaft | Combating fungi with substituted triazolylalkyl pyridyl ethers |
| WO2002069715A2 (de) * | 2001-03-06 | 2002-09-12 | Bayer Cropscience Ag | Beizmittel |
| WO2002069715A3 (de) * | 2001-03-06 | 2003-03-20 | Bayer Ag | Beizmittel |
| WO2007065843A2 (de) * | 2005-12-09 | 2007-06-14 | Basf Se | Verwendung von gibberellin als safener für azole zur bekämpfung von schadpilzen |
| WO2007065843A3 (de) * | 2005-12-09 | 2007-11-15 | Basf Ag | Verwendung von gibberellin als safener für azole zur bekämpfung von schadpilzen |
| WO2008155416A2 (en) * | 2007-06-20 | 2008-12-24 | Basf Se | Gibberellins as safeners for fungicides with phytotoxic activity |
| WO2008155416A3 (en) * | 2007-06-20 | 2009-06-18 | Basf Se | Gibberellins as safeners for fungicides with phytotoxic activity |
Also Published As
| Publication number | Publication date |
|---|---|
| NO762585L (US07582779-20090901-C00044.png) | 1977-02-08 |
| NL7608715A (nl) | 1977-02-09 |
| GB1491856A (en) | 1977-11-16 |
| AU1655376A (en) | 1978-02-09 |
| FI762251A (US07582779-20090901-C00044.png) | 1977-02-08 |
| BE844909A (fr) | 1977-02-07 |
| FR2320052A1 (fr) | 1977-03-04 |
| TR18802A (tr) | 1977-11-01 |
| FR2320052B3 (US07582779-20090901-C00044.png) | 1979-05-04 |
| DK355876A (da) | 1977-02-08 |
| CS189022B2 (en) | 1979-03-30 |
| JPS5221330A (en) | 1977-02-17 |
| SE7608798L (sv) | 1977-02-08 |
| DD126843A5 (US07582779-20090901-C00044.png) | 1977-08-17 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| EP1651040B1 (de) | Fungizide ternäre wirkstoffkombinationen | |
| DE2560510C2 (US07582779-20090901-C00044.png) | ||
| CH658654A5 (de) | Azolderivate, verfahren zu ihrer herstellung und mittel die diese verbindungen enthalten. | |
| EP0088256B2 (de) | Fungizide Mittel | |
| DE2325156A1 (de) | Fungizide und mikrobizide mittel | |
| DE4139637A1 (de) | Fungizide wirkstoffkombinationen | |
| EP1677600B1 (de) | Fungizide wirkstoffkombinationen enthaltend spiroxamine, prothioconazole und tebuconazole | |
| DE2535332A1 (de) | Fungizide mittel | |
| EP0190561B1 (de) | Mittel zur Regulierung des Pflanzenwachstums | |
| DE3605551A1 (de) | Fungizide mittel | |
| DE3234624A1 (de) | Fungizide mittel | |
| DE3721852A1 (de) | Fungizide saatgutbehandlungsmittel | |
| EP0437744B1 (de) | Fungizide Wirkstoffkombinationen | |
| EP1235484B1 (de) | Fungizide wirkstoffkombinationen | |
| DE19633502A1 (de) | Verwendung von Lipo-Chitooligosacchariden zur Verbesserung der Wirksamkeit von Fungiziden | |
| EP0833561B1 (de) | Fungizide wirkstoffkombinationen | |
| EP0513567B1 (de) | Fungizide Wirkstoffkombinationen | |
| EP1339287B1 (de) | Fungizide wirkstoffkombinationen | |
| DE3736651C2 (de) | Fungizide Wirkstoffkombinationen | |
| DE19649459C2 (de) | Fungizide Wirkstoffkombinationen | |
| EP0106105B1 (de) | Fungizide Mittel | |
| DE10059609A1 (de) | Fungizide Wirkstoffkombinationen | |
| DE2453210C3 (de) | Bekämpfung von Pilzen der Gattung Hehmnthosporium mit Dimethyipyrazolylbenzimidazol | |
| DE3715705A1 (de) | Fungizide wirkstoffkombinationen | |
| DE2922481A1 (de) | Elektroparasitizide mittel enthaltend substituierte phenoxybenzyloxycarbonylderivate, (ihio)phosphorsaeureester, verfahren zu ihrer herstellung und ihre verwendung als ektoparasitizide |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| OHN | Withdrawal |