PL94007B1 - - Google Patents
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- PL94007B1 PL94007B1 PL1974172460A PL17246074A PL94007B1 PL 94007 B1 PL94007 B1 PL 94007B1 PL 1974172460 A PL1974172460 A PL 1974172460A PL 17246074 A PL17246074 A PL 17246074A PL 94007 B1 PL94007 B1 PL 94007B1
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- Poland
- Prior art keywords
- spp
- viii
- residue
- plants
- active substance
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- 125000004186 cyclopropylmethyl group Chemical group [H]C([H])(*)C1([H])C([H])([H])C1([H])[H] 0.000 description 1
- MNNHAPBLZZVQHP-UHFFFAOYSA-N diammonium hydrogen phosphate Chemical compound [NH4+].[NH4+].OP([O-])([O-])=O MNNHAPBLZZVQHP-UHFFFAOYSA-N 0.000 description 1
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- 239000012895 dilution Substances 0.000 description 1
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- 229950004394 ditiocarb Drugs 0.000 description 1
- 239000010459 dolomite Substances 0.000 description 1
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- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 description 1
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- BXWNKGSJHAJOGX-UHFFFAOYSA-N hexadecan-1-ol Chemical class CCCCCCCCCCCCCCCCO BXWNKGSJHAJOGX-UHFFFAOYSA-N 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
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 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 1
- 239000003350 kerosene Substances 0.000 description 1
- 239000004571 lime Substances 0.000 description 1
- 239000006028 limestone Substances 0.000 description 1
- 239000000395 magnesium oxide Substances 0.000 description 1
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 1
- 235000012245 magnesium oxide Nutrition 0.000 description 1
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 1
- 235000019341 magnesium sulphate Nutrition 0.000 description 1
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 235000010755 mineral Nutrition 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- SLFVYFOEHHLHDW-UHFFFAOYSA-N n-(trifluoromethyl)aniline Chemical compound FC(F)(F)NC1=CC=CC=C1 SLFVYFOEHHLHDW-UHFFFAOYSA-N 0.000 description 1
- KTGXLLOZXLZOIA-UHFFFAOYSA-N n-cyclopropyl-2,6-dinitro-n-propyl-4-(trifluoromethyl)aniline Chemical compound [O-][N+](=O)C=1C=C(C(F)(F)F)C=C([N+]([O-])=O)C=1N(CCC)C1CC1 KTGXLLOZXLZOIA-UHFFFAOYSA-N 0.000 description 1
- MONYWWWQBHZMIZ-UHFFFAOYSA-N n-ethyl-2,6-dinitro-n-(oxolan-2-ylmethyl)-4-(trifluoromethyl)aniline Chemical compound [O-][N+](=O)C=1C=C(C(F)(F)F)C=C([N+]([O-])=O)C=1N(CC)CC1CCCO1 MONYWWWQBHZMIZ-UHFFFAOYSA-N 0.000 description 1
- PSZYNBSKGUBXEH-UHFFFAOYSA-N naphthalene-1-sulfonic acid Chemical class C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-N 0.000 description 1
- SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical compound CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000002798 polar solvent Substances 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 235000019814 powdered cellulose Nutrition 0.000 description 1
- 229920003124 powdered cellulose Polymers 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- 150000003254 radicals Chemical class 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- 125000005624 silicic acid group Chemical class 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 238000009331 sowing Methods 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-L sulfite Chemical compound [O-]S([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-L 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 230000002195 synergetic effect Effects 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 239000002641 tar oil Substances 0.000 description 1
- LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical group C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 description 1
- CXWXQJXEFPUFDZ-UHFFFAOYSA-N tetralin Chemical compound C1=CC=C2CCCCC2=C1 CXWXQJXEFPUFDZ-UHFFFAOYSA-N 0.000 description 1
- 229960000278 theophylline Drugs 0.000 description 1
- ZFXYFBGIUFBOJW-UHFFFAOYSA-N theophylline Chemical compound O=C1N(C)C(=O)N(C)C2=C1NC=N2 ZFXYFBGIUFBOJW-UHFFFAOYSA-N 0.000 description 1
- 229940047183 tribulus Drugs 0.000 description 1
- ZSDSQXJSNMTJDA-UHFFFAOYSA-N trifluralin Chemical compound CCCN(CCC)C1=C([N+]([O-])=O)C=C(C(F)(F)F)C=C1[N+]([O-])=O ZSDSQXJSNMTJDA-UHFFFAOYSA-N 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
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Classifications
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03H—HOLOGRAPHIC PROCESSES OR APPARATUS
- G03H1/00—Holographic processes or apparatus using light, infrared or ultraviolet waves for obtaining holograms or for obtaining an image from them; Details peculiar thereto
- G03H1/04—Processes or apparatus for producing holograms
Landscapes
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
Opis patentowy opublikowano: 30.10.1978 94007 MKP A01n9/02 Int. Cl2. A01N9/02 Twórcawyna lazku: Uprawniony z patentu: BASF Aktiengesellschaft, Ludwigshafen (Republika Federalna Niemiec) Srodek chwastobójczy Niniejszy wynalazek dotyczy srodków chwastobójczych, w szczególnosci selektywnych srodków chwastobójczych nadajacych sie do zwalczania niepozadanych roslin.Znane jest stosowanie jako srodków chwastobójczych podstawionych dwunitroanilin i tiolokarbaminianów, z opisu patentowego Stanów Zjednoczonych Ameryki nr 3185780. Ich dzialanie jednak nie zawsze jest zadowalajace.Stwierdzono, ze dobre dzialanie chwastobójcze wykazuja srodki chwastobójcze zawierajace mieszanine zlozona ze zwiazku o wzorze 1, w którym X oznacza nizszy rodnik alkilowy, chlorowcoalkilowy, alkilosulfonylowy, metoksylowy, aminosulfonylowy; Y oznacza wodór lub grupe aminowa; F^ oznacza reszte tetrahydrofurfurylowa, cyklopropylowa albo cyklopropylometylowa, wzglednie nizszy rodnik alkilowy, alkeny- lowy lub alkinylowy, ewentualnie podstawione chlorowcem albo grupa alkoksylowa; R oznacza reszte alkoksyal- kilowa, propionometyloamidowa lub nizszy rodnik alkilowy, alkenylowy albo alkjnylowy, ewentualnie podsta¬ wione chlorowcem i zwiazku o wzorze 2, w którym R oznacza rodnik alkilowy, alkenylowy albo alkinylowy, dwu- lub trójcykloalkilowy wzglednie reszte cykloalkilowa, ewentualnie podstawiona rodnikiem alkilowym; Ri oznacza wodór lub reszte alifatyczna do 4 atomów C; R2 reszte alkilowa, alkenylowa, alkinylowa, ewentualnie podstawione chlorowcem lub grupa alkoksylowa, reszte benzylowa, ewentualnie podstawiona chlorowcem.Mieszaniny moga zawierac jeden lub wiecej zwiazków o wzorze 1 i/lub jeden lub wiecej zwiazków o wzorze 2. Proporcje w mieszaninie mozna dobierac dowolnie; korzystnie sa mieszaniny 0,1-10 czesci wagowych zwiazków o wzorze 1 i 0,1—10 czesci wagowych zwiazków o wzorze 2. Stosowane ilosci substancji czynnej wynosza 0,1-15 kg na hektar, korzystnie 0,1-5 kg na hektar.Srodki wedlug wynalazku dzialaja selektywnie w stosunku do Beta spp., Alium cepa, Pisum sativum, Gladiolus spp., Soja hispida, Goscypium hirstutum, Phascolus vulgarisr Arachis hypogaca i innych.Srodki wedlug wynalazku stosuje sie np. w postaci nadajacych sie do bezposredniego rozpylania roztworów, proszków, zawiesin lub dyspersji, emulsji, dyspersji olejowych, past, srodków pylistych, srodków do rozsiewania, granulatów, droga spryskiwania, zamglawiania, rozpylania, rozsiewania lub polewania. Postaci2 94 007 uzytkowe uzaleznione sa calkowicie od celu stosowania; kazdorazowo powinny one zapewniac mozliwie dokladny rozdzial substancji czynnych.Dla przygotowania roztworów, emulsji, past i dyspersji olejowych dla bezposredniego rozpylania, wchodza w rachube frakcje olejów mineralnych o sredniej do wysokiej temperaturze wrzenia jak nafta lub olej napedowy, ponadto oleje smolowe itd. jak równiez oleje roslinne i zwierzece, alifatyczne, cykliczne i aromatyczne weglowodory np. benzen, toluen, ksylen, olej parafinowy, tetrahydronaftalen, alkilowane naftaleny, lub ich pochodne np. metanol, etanol, propanol, butanol, chloroform, czterochlorek wegla, cykloheksanol,cykloheksa- non, chlorobenzen, izoforon itd., silnie polarne rozpuszczalniki np. dwumetyloforrnamid, dwumetylosulfotlenek, N-metylopiroJidon, woda itd.Wodne formy uzytkowe mozna przygotowywac z koncentratów emulsyjnych, past lub zwilzalnych proszków, dyspersji olejowych przez dodanie wody. Dla sporzadzania emulsji, past lub dyspersji olejowych mozna przy pomocy srodków zwilzajacych, adhezyjnych, dyspergujacych lub emulgujacych homogenizowac te substancje w wodzie jako takie albo rozpuszczone woleju lub rozpuszczalniku. Mozna równiez sporzadzac z substancji czynnej, srodka zwilzajacego, adhezyjnego, dyspergujacego lub emulgujacego oraz ewentualnie rozpuszczalnika albo oleju koncentraty nadajace sie do rozcienczania woda.Jako srodki powierzchniowo czynne mozna wymienic: ligninosulfoniany metali alkalicznych, metali ziem alkalicznych i amonu, kwasy naftalenosulfonowe, fenolosulfonowe,alkiloarylosulfoniany, alkilosiarczany, alkilo- sulfoniany, dwubutybnaftalenosulfoniany metali alkalicznych i metali ziem alkalicznych, siarczan eteru laurylo- wego, siarczany alkoholi tluszczowych, sole kwasów tluszczowych i metali alkalicznych oraz metali ziem alkalicznych, sole siarczanowanych heksadekanoli, heptadekanoli, oktadekanoli, sole siarczanowanego eteru glikolu i alkoholu tluszczowego, produkty kondensacji sulfonowanego naftalenu i pochodnych naftalenu z for¬ maldehydem, produkty kondensacji naftalenj wzglednie kwasów naftalenosulfonowych z fenolem i formaldehy¬ dem, eter polioksyetylenooktylofenolowy, etoksylowany izooktylofenol, oktylofenol, nonylofenol, eter alkilofe- nolopoliglikolowy, eter trójbutylofenylopoliglikolowy, alkiloarylopolieteroalkohole, alkohol izotridecylowy, addukty alkoholu tluszczowego i tlenku etylenu, etoksylowany olej rycynowy, eter polioksyetyienoalkilowy, etoksylowany polioksypropylen, acetal alkoholu laurylowego i eteru poliglikolowego, estry sorbitu, lignine, lugi posulfitowe i metyloceluloze.Proszki, srodki do rozsiewania i srodki pyliste mozna sporzadzac przez mieszanie lub wspólny przemial substancji czynnych ze stalym nosnikiem.Granulaty, np. granulaty otoczkowe, impregnatowe i homogeniczne, mozna wytwarzac przez wiazanie substancji czynnych na stalych nosnikach. Stalymi nosnikami sa np. materialy mineralne jak silikazel, kwasy krzemowe, zele krzemionkowe, krzemiany, talk, kaolin, attaclay, wapien, wapno, kreda, bolus, less, glina, dolomit, ziemia okrzemkowa, siarczan wapnia i magnezu, tlenek magnezu, zmielone tworzywa sztuczne, nawozy jak np. siarczan amonu, fosforan amonu, azotan amonu, moczniki oraz produkty roslinne jak maki zbozowe, maczka z kory drzewnej, maczka drzewna i ze skorup orzecha, sproszkowana celuloza i inne stale nosniki.Zestawy zawieraja pomiedzy 0,1 i 95% wagowych substancji czynnej, korzystnie pomiedzy 0,5 i 90% wagowych.Do mieszanin lub poszczególnych substancji czynnych mozna dodawac rózne typy olejów, srodki chwastobójcze, grzybobójcze, nicieniobójcze, owadobójcze, bakteriobójcze, mikroelementy, nawozy, srodki przeciw pienieniu (np. silikony), regulatory wzrostu, odtrutki lub inne zwiazki o dzialaniu chwastobójczym, wdanym przypadku równiez dopiero bezposrednio przed uzyciem mieszania w zbiorniku.Wymienione na koncu zwiazki dzialajace chwastobójczo mozna stosowac równiez przed poszczególnymi substancjami czynnymi wedlug wynalazku lub mieszaninami albo po nich. Dodawarne tych srodków do srodków chwastobójczych wedlug wynalazku moze nastepowac w proporcji wagowej 1 : 10—10 :1. To samo dotyczy olejów, srodków grzybobójczych, nicieniobójczych, owadobójczych, bakteriobójczych, odtrutek i regulatorów wzrostu.Srodki wedlug wynalazku mozna stosowac jednorazowo lub wielokrotnie m.in. przed sadzeniem, po sadzeniu, sposobem przedsiewnym, przedwschodowym, powschodowym albo podczas wschodzenia roslin uprawnych lub roslin niepozadanych. Ilosci uzytkowe srodków wedlug wynalazku sa zmienne. Stosowana dawka zalezy glównie od rodzaju zadanego efektu. Wskaznik zuzycia wynosi na ogól od 0,1—15 i wiecej kg substancji czynnej na hektar, korzystnie od 0,2—6 kg na hektar.Nowe srodki wykazuja silne dzialanie chwastobójcze i z tego wzgledu mozna je stosowac do niszczenia chwastów wzglednie do zwalczania niepozadanej wegetacji. Dzialanie totalne czy tez selektywne nowych srodków zalezy glównie od ilosci substancji czynnej na jednostke powierzchni. Przez chwasty wzglednie niepozadana wegetacje nalezy rozumiec wszystkie rosliny jedno- i dwuliscienne, które rosna w miejscach w których sa niepozadane.Tak wiec przy pomocy srodków wedlug wynalazku mozna zwalczac na przyklad: trawy, jak: Cynodon94 007 3 spp., Digitaria spp., Echinochloa spp., Setaria spp., Panicum spp., Alopecurus spp., Lolium spp., Sorghum spp., Agropyron spp., Phalaris spp., Apera spp., Dactylis spp., Avena spp., Bromus spp., Uniola spp., Poa spp., Leptochloa spp., Brachiaria spp., Eleusine spp., Cenchrus spp., Eragrostis spp., i inne; Cyperaceae, jak: Carex spp., Cyperus spp., Eleocharis spp., Scirpus spp., i inne; dwuliscienne chwasty jak: Malvaceae, np. Abutilon theoprasti, Sida spp., i inne, Hibiscus spp., Malva spp., Composiae, jak: Ambrosia spp., Lactuca spp., Senecio spp., Sonchus spp., Xanthium spp., Iva spp., Galinsoga spp., Taraxacum spp., Chrysanthemum spp., Cirsium spp., Centaurea spp., Tussilago spp., Lapsana communis, Tagetes spp., Erigeron spp., Anthemis spp., Matricaria spp., Artemisia spp., Bidens spp., i inne; Convolvulaceae, jak: Convolvulus spp., Ipoea spp., i inne, Cuscuta spp., Jaquemontia tamnifolia; Cruciferae, jak: Barbarea vulgaris, Brassica spp., Capsella spp., Sisymbrium spp., Thlaspi spp., Sinapio arvensis, Arabidopsis thaliana, Descurainia spp., Drabe spp., Coronopus didymus, Lepidium spp., Raphanus spp., i inne; Geraniaceae, jak: Erodium spp.. Geranium spp., i inne; Portulacaceae, jak: Portulaca spp., i inne; Primulaceae, jak: Anagallis arvensis, Lysi machia spp., i inne; Rubiaceae, jak: Richardia spp., Galium spp., Diodia spp., i inne; Scrophularia- ceae, jak: Linaria spp., Veronica spp.. Digitalis spp., i inne; Solanaceae, jak: Physalisspp., Solanum spp., Nicandra spp., Datura spp., i inne; Urticaceae, jak: Urtica spp., Violaceae, jak: Viola spp., i inne; Zygophyllaceae, jak: Tribulus terrestis i inne; Euphorbiaceae, jak: Mercurialis annua, Euphorbia spp., Umbelliferae, jak: Daucus carota, Aethusa cynapium, Ammi majus i inne; Commelinaeae, jak: Commel i na spp., i inne; Labiatae, jak: Lamium spp., Galeopsis spp., i inne; Laguminosae, jak: Medicago spp., Trifolium spp., Vicia spp., Sesbania exaltata, Cassia spp., Lathyrus spp., i inne; Plantaginaceae, jak: Plantago spp., i inne; Polygonaceae, jak: Polygonum spp., Fagopyrum spp.; Rumex spp., i inne; Aizoaceae, jak: MoHugo verticillata i inne; Amaranthus spp., i inne; Boraginaceae, jak: Amsinckia spp., Myostis spp., Anchusa spp., Lithospermum spp., i inne; Caryophyllaceae, jak: Stellaria spp., Spergula spp., Saponaria spp.. Seleranthus ar.nuus, Silene spp., Cerastium spp., Agrostemma githago, i inne; Chenopodiaceae, jak: Chenopodium spp., Kochia spp., Salsola Kali, Atriplex spp:, Monolepsis nuttalliana i inne; Lythraceae, jak: Cuphea spp., i inne; Oxalidaceae, jak: Oxalis spp., Ranunculaceae, jak: Ranunczlus spp., Adonis spp., Delphinium spp., i inne; Papveraceae, jak: Papaver spp., Fumaria officinalis, i inne; Onagraceae, jak: Jussiae spp., i inne; Rosaceae, jak: Alchemillia spp., Potentilla spp., i inne; Potamogetonaceae, jak: Potamogeton spp., i inne; Najdaceae, jak: Majas spp., i inne; Marsileaceae, jak: Marsilea quadrifolia i inne.Na roslinach wymienionych w przykladach wypróbowywano w szklarni i na polu nastepujace zwiazki uzyte w mieszaninach: N-etylo-N-butylo-2,6-dwunitro-4-trójfluorometyloanilina, N,N-dwu-(n-propylo)-2,6-dwunitro-4-trójfluorometyloanilina, N-propylo-N-j3-chloróetylo-2,6-dwunitro-4*trójfluorometyloanilina, N-allilo-N^3-chloroetylo-2,6-dwunitro-4-trójfluorometyloanilina, N-etylo-N^-chloroetylo-2,6-dwunitro-4-trójfluorometyloanilina, N-etylo-N-^^bromoetylo-2,6-dwunitro-4-trójfluorometyloanilina, N-propylo-N-j3-bromoetylo-2,6-dwunitro-4-trójfluorometyloanilina, N-^-metoksyetylo-N-j3-chloroetylo-2,6-dwunitro-4-trójfluorometyloanilina, N-izopropylo-N-propargilo-2,6-dwunitro-4-trójfluorometyloanilina, N-propylo-N-allilo-2,6-dwunitro-4-trójfluorometyloanilina, N-propylo-N-propargilo-2,6-dwunitro-4-trójfluorometyloanilina, N,N-bis-(j8-chloroetylo)-2,6-dwunitro-4-trójfluorometyloanilina, N,N-bis-(j3-metoksyetylo)-2,6-dwunitro-4-trójfluorometyloanilina, N-propylo-N-cyklopropylo-2,6-dwunitro-4-trójfluorometyloanilina, N-propylo-N-tetrahydrofurfurylo-2,6-dwunitro-4-trójfluorometyloanilina, N-etylo-N-tetrahydrofurfurylo-2,6-dwunitro-4-trójfluorometyloanilina, N-propylo-N-cyklopropyloametylo-2,6-dwunitro-4-trójfluorometyloanilina, N-propylo-N-allilo-2,6-dwunitro-4-metylosulfonyloanilina, N,N-bis-(n-propylo)-2,6-dwunitro-4-metylosulfonyloanilina, N,N-bis-(n-propylo)-2,6-dwunitro-4-aminosulfonyloanilina, N,N-bis-(n-propylo)-2,6-dwunitro-4-rnetyloanilina, N,N-bis-(llTz.-butylo)-2,6-dwunitro-4-lll.rz.butyloanilina, N,N-bis-(n-propylo)-2,6-dwunitro-4-izopropyloanilina, N,N-dwuetylo-2,6-dwunitro-3-amino-4-fluorometyloanilina, N-metylo-N-(3-chloroetylo-2r6-dwunitro-4-metyloanilina, N,N-bis-(n-propylo)-2,6-dwunitro-4-metoksyanilina,4 94 007 N,N-bis-(/J-chloroetylo)-2,6-dwunitro-4-metyloanilina, N,N-dwuizopropylotiolokarbaminian 2,3-dwuchloroallilu, 2-(2,6-dwumtro-4-toluidyno)-N-propionometylamid, N,N-dwuizopropylotiolokarbaminian 2,3,3-trójchloroallilu, N-etylo-N-butylotiolokarbaminian n-propylu, N,N-dwu-(n-propylo)-tiolokarbaminian etylu, N,N-dwu-(n-propylo)-tiolokarbaminian n-propylu, N,N-dwu-(n-propylo)-tiolokarbaminian-l I l-rz.butylu, N,N-dwuizobutylotiolokarbaminian etylu, N,N-dwu-(n-butylo)-tiolokarbaminian etylu, NfN-dwuetylotiolokarbaminian butylu, N,N-dwuetylodwutiokarbaminian 2-chloroallilu, N-etylo-N-cykloheksylotiolokarbaminian etylu, N-dwucyklo-(2,2,1)-heptylo-N-etylotiolokarbaminian etylu, N-1 lub 2-dwucyklo-(3/3,0)-oktylo-N-etylotiolokarbaminian etylu, N,N-dwuetylotiolokarbaminian p-chlorobenzylu, N-dwucyklo-(2,2,1 )-heptylo-N-etylodwutiokarbaminian etylu, N-1 lub 2-dwucyklo-(3,3,0)-N-etylotiolokarbaminian izopropylu, N-propargilo-N-cykloheksylotiolokarbaminian etylu, N-etylo-N-o-metylocykloheksylotiolokarbaminian etylu.Uzyte ilosci substancji czynnej wynosily 0,1—15 kg/ha. Podczas tych prób okazalo sie, ze wymienione zwiazki sa odpowiednio skuteczne biologicznie, jak i mieszaniny przytoczone w przykladach I—II.Przyklad I. Rolna powierzchnie uzytkowa obsiano róznymi nasionami. Bezposrednio potem potrak¬ towano tak przygotowana glebe nastepujacymi odrebnymi substancjami czynnymi i ich mieszaninami w postaci pasty: I N,N-dwu-(n-propylo)-2,6-dwunitro-4-trójfluorometyloanilina 11 N-n-propylo-N-0-chloroetylo-2,6-dwunitro-4-trójfluorometyloanilina IV N,N-dwu-(n-propylo)-2,6-dwunitro-4-aminosulfonyloanilina V N,N-dwuizopropylotiolokarbaminian 2,3-dwuchloroallilu VI N,N-dwuizopropylotiolokarbaminian 2,2,3-trójchloroallilu VIII N-etylo-N-cykloheksylotiolokarbaminian etylu wilosciach po 0,25, 0,5, 0,75 M kg/ha substancji aktywnej l+VIM, ll+VIII, IV+VIM, ll+V, ll+VI, IV+V i IV+VI wdanym przypadku w ilosciach 0,75+0,25, 0,25+0,25 i 0,25+0,75 kg/ha substancji aktywnej.Po 3—4 tygodniach stwierdzono, ze mieszaniny wykazywaly lepsze dzialanie chwastobójcze niz substancje czynne I, II, IV, V, VI i VIII, przy jednakowej tolerancji przez rosliny uprawne.Wyniki prób podano w tablicy I, w której w nawiasach podano dzialanie pojedynczych substancji czynnych, stosowanych w analogicznej ilosci. Z porównania sumy dzialania substancji i pojedynczych z efektem wywolanym przez mieszanke wedlug wynalazku wynika wyraznie efekt synergetyczny srodka wedlug wynalaz¬ ku.Przyklad II. Rózne rosliny po osiagnieciu wysokosci od 2—12 cm traktowano w szklarni dyspersjami olejowymi nastepujacych poszczególnych substancji czynnych i ich mieszaninami: I N,N-dwu-(n-propylo)-2,6-dwunitro-4-trójfluorometyloanilina II N-n-propylo-N-^-chloroetylo-2,6-dwunitro-4-trójfluorometyloanilina IV N,N-dwu-(n-propylo)-2,6-dwunitro-4-aminosulfonyloanilina V N,N-dwuizopropylotiolarbaminian 2,3-dwuchloroallilu VI N,N-dwuizopropylotiolokarbaminian 2,3,3-trójchloroallilu VIII N-etylo-N-cykloheksylotiolokarbaminian etylu wilosciach po 0,25, 0,5, 0,75 i1 kg/ha substancji aktywnej l+VIII, ll+VIII, IV+VIII, ll+V, IV+V, l+VII, ll + VII i IV+VII w ilosciach po 0,25+0,75, 0,25+0,25, 0,75+0,25 kg/ha substancji aktywnej.Po 2—3 tygodniach stwierdzono, ze mieszaniny wykazywaly lepsze dzialanie chwastobójcze niz posz¬ czególne substancje czynne, przy jednakowej tolerancji przez rosliny uprawne.Wyniki prób podano w tablicy II.94 007 5 PL
Claims (1)
1. Zastrzezenie patentowe Srodek chwastobójczy, znamienny tym, ze zawiera mieszanine zwiazku o wzorze 1, w którym X oznacza nizszy rodnik alkilowy, chlorowcoalkilowy, alkilosulfonylowy, metoksylowy, aminosulfonylowy, X oznacza wodór lub grupe aminowa, Rx oznacza reszte tetrahydrofurfurylowa, cyklopropylowa lub cyklopro- pylometylowa albo nizszy rodnik alkilowy, alkenylowy wzglednie alkinylowy, ewentualnie podstawione chlorowcem lub grupa a Ikoksy Iowa, R oznacza reszte alkoksyalkilowa albo propionometyloamidowa lub nizszy rodnik alkilowy, alkenylowy wzglednie alkinylowy, ewentualnie podstawione chlorowcem i zwiazku o wzorze 2, w którym R oznacza rodnik alkilowy, alkenylowy, alkinylowy, dwu- lub trójcykloalkilowy albo reszte cykloalki- lowa, ewentualnie podstawiona rodnikiem alkilowym, Rt oznacza wodór lub reszte alifatyczna do 4 atomów C, R2 —oznacza reszte alkilowa, alkenylowa, alkinylowa, ewentualnie podstawione chlorowcem albo grupa alkoksylowa, reszte benzylowa, ewentualnie podstawiona chlorowcem.Tablica I Substancja czynna kg/ha Rosliny uzytkowe Beta vulgaris Rosliny niepozadane Alopecurus myosuroides Avena fatua Digitaria sanguinalis Echinochloa crus—galli Setaria faberii Stellaria media 0,25 0 23 18 25 32 37 5 0,5 0 41 34 45 50 46 7 I 0,75 0 50 45 56 58 55 10 1 0 63 51 70 70 65 16 0,25 0 20 15 30 30 35 5 0,5 0 40 30 57 45 60 6 II 0,75 0 52 43 70 58 74 11 1 0 60 50 85 75 90 13 0,25 0 20 14 28 34 33 5 IV 0,5 0 36 30 55 50 58 8 0,75 0 45 37 68 65 70 10 1 0 58 48 84 76 87 15 0,25 0 11 10 0 0 2 6 V 0,5 0 26 20 3 6 5 7 0,75 0 45 35 5 10 8 10 1 0 58 50 9 16 10 13 0,25 0 15 15 3 5 4 3 VI 0,5 0 30 25 5 10 7 7 0,75 0 46 45 7 16 10 10 1 0 60 60 10 20 15 15 0,25 0 10 5 15 15 12 5 VI 0,5 0 15 10 32 25 27 12 II 0,75 0 40 15 40 39 35 17 1 0 68 27 50 48 45 20 Tablica I (c.d.) Substancja czynna j kg/ha Rosliny uzytkowe Beta vu!garis Rosliny niepozadane Alopecurus myosuroides Avena fatua Digitaria sanguinalis Echinochloa crus—gali Setaria faberii Stellaria media 0,75+0,25 0 (50+10) 90 (45+5) 85 (56+15) 98 (57 + 15) 96 (F5 + 12) 95 (10 + 5) 46 l+VIII 0,25+0,25 0 60 64 70 75 78 40 0,25+0,75 0 (23+40) 92 (18+15) 66 (25+40) 92 (32+39) 98 (37+35) 98 (5+17) 50 0,75+0,25 0 (52+10) 96 (43+5) 75 (70+15) 100 (58+15) 100 (74+12) 100 (11+5) 45 ll+VIII 0,25+0,25 0 64 50 70 72 75 40 0,25+0,75 0 (20+40) 93 (15+15) 62 (30+40) 98 (30+39) 96 (35+25) 99 (3+17) 52 0,75+0,25 0 (45+10) 80 (37+5) 70 (68+15) 100 -(65+15) 100 (70+12) 100 (10+5) 44 IV+VIII 0,25+0,25 0 60 62 75 73 78 40 0,25+0,75 0 (20+40) 88 (14 + 15) 65 (28+40) 95 (34 + 39) 100 (33+35) 94 (5 + 17) 53 co -u o oTablica I (c.d.) Substancja czynna kg ha I + V II + V IV + V IV + VI Rosliny uzytkowe Beta vulgaris Rosliny niepozadane Alopecurus myosuroides Avena fatua Digitaria sanguinalis Echinochloa crus—galli Setaria faberii Stelaria media 0 (52+11) 93 (43+10) 84 (70+0) 98 (58+0) 92 (74+2) 97 (11+6) 50 0 63 50 60 61 65 40 0 90 80 68 68 75 43 0 (52+15) 98 (43+15) 92 (70+3) 98 (58+5) 90 (74+4) 100 (11+3) 40 0 62 65 66 65 72 40 0 95 85 70 81 80 44 0 (45+11) 96 (37+10) 80 (68+0) 100 (65+0) 100 (70+2) 100 (10+6) 50 0 60 49 55 60 69 41 0 90 84 65 75 74 49 0 (45+15) 92 (37+15) 80 (68+3) 98 (65+5) 98 (70+4) 100 (10+3) 43 0 60 65 64 70 60 40 0 90 84 66 74 65 45 co c o Tablica II Substancja czynna kg/ha Rosliny uzytkowe Beta vulgaris Rosliny niepozadane Alopecurus myosuroides Echinochloa crus—galli Avena fatua Stellaria media 0,25 0 15 10 5 0,5 0 25 15 12 I 0,75 0 30 19 22 1 0 38 25 30 0,25 0 13 15 6 0,5 0 24 20 10 II 0,75 0 35 30 17 1 0 42 37 25 0,25 0 10 11 5 I 0,5 0 18 16 9 V 0,75 0 23 20 15 1 0 30 30 21 0,25 0 10 5 10 1 0,5 0 20 10 15 3 V 0,75 0 25 18 24 5 1 0 35 25 35 7 0,25 0 7 5 10 2 VI 0,5 0 13 15 18 3 0,75 0 20 20 25 5 1 0 30 25 35 8 0,25 0 5 7 4 0 VIII 0,5 0 7 12 5 5 0,75 0 10 15 12 7 1 0 18 20 20 10Tablica II (c.d.) oo Substancja czynna kg/ha Rosliny uzytkowe Beta vulgaris Rosliny niepozadane Alopecurus myosuroides Avena fatua Echinochloa crus—gal ii Stel lar ia media 0,25+ + 0,75 0 50 48 54 42 l + VIII 0,25+ +0,25 0 47 44 45 30 0,75+ +0,25 0 (30+5) 62 (25+4) 58 (14+7) 52 (22+0) 50 0,25+ +0,75 0 53 45 62 45 ll+VIII 0,25+ +0,25 0 46 40 51 29 0,75+ +0,25 0 (35+5) 70 (20+4) 52 (30+7) 64 (17+0) 48 0,25 + +0,75 0 48 45 55 38 IV+VIII 0,25+ +0,25 0 46 35 54 36 0,75+ +0,25 0 (23+5) 56 (11+4) 42 (20+7) 56 (15+0) 42 0,25+ +0,75 0 66 57 60 40 ll+V 0,25+ +0,25 0 46 43 50 35 0,75+ +0,25 0 (35+10) 70 (20+10) 56 (30+5) 63 (17+1) 46 0,25+ +0,75 0 60 57 62 43 IV+VI 0,25+ +0,25 0 45 42 45 35 0,75 + +0,25 0 (23 + 7) 58 (11+10) 50 (20 +5) 53 (15+2) 45 co O o 0 = bez uszkodzen 100 = calkowite zniszczenie94 007 ,N02 R Y NO R 2 WZÓR 1 R 1 X N-C-S-R R o WZdR2 PL
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE19732334563 DE2334563A1 (de) | 1973-07-07 | 1973-07-07 | Herbizid |
Publications (1)
Publication Number | Publication Date |
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PL94007B1 true PL94007B1 (pl) | 1977-07-30 |
Family
ID=5886189
Family Applications (1)
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PL1974172460A PL94007B1 (pl) | 1973-07-07 | 1974-07-05 |
Country Status (24)
Country | Link |
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JP (1) | JPS5036636A (pl) |
AR (1) | AR217032A1 (pl) |
BE (1) | BE817305A (pl) |
BG (2) | BG22056A3 (pl) |
BR (1) | BR7405534D0 (pl) |
CH (1) | CH585005A5 (pl) |
CS (1) | CS189658B2 (pl) |
DD (1) | DD111778A5 (pl) |
DE (1) | DE2334563A1 (pl) |
DK (1) | DK137742C (pl) |
ES (1) | ES428035A1 (pl) |
FR (1) | FR2235645B1 (pl) |
GB (1) | GB1471772A (pl) |
HU (1) | HU169820B (pl) |
IL (1) | IL45060A (pl) |
IT (1) | IT1049296B (pl) |
LU (1) | LU70472A1 (pl) |
NL (1) | NL7409071A (pl) |
NO (1) | NO742394L (pl) |
PL (1) | PL94007B1 (pl) |
RO (1) | RO69333A (pl) |
SE (1) | SE7408882L (pl) |
SU (1) | SU579844A3 (pl) |
ZA (1) | ZA744217B (pl) |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
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JPS5520919A (en) * | 1978-07-31 | 1980-02-14 | Nihon Radiator Co | Parts connecting method to aluminium pipe |
DE2909158A1 (de) * | 1979-03-08 | 1980-09-11 | Basf Ag | Herbizide mischungen |
PT82293B (en) * | 1985-04-08 | 1988-01-11 | Stauffer Chemical Co | Process for the preparation of synergetic herbicide compositions containing a tiolcarbamate and a by product with benzene |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
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US3449111A (en) * | 1966-12-08 | 1969-06-10 | Lilly Co Eli | Method of eliminating weeds |
US3518076A (en) * | 1967-05-17 | 1970-06-30 | Lilly Co Eli | Method of fliminating weed species with herbicidal combination |
-
1973
- 1973-07-07 DE DE19732334563 patent/DE2334563A1/de not_active Withdrawn
-
1974
- 1974-06-17 AR AR254225A patent/AR217032A1/es active
- 1974-06-17 BG BG26996A patent/BG22056A3/xx unknown
- 1974-06-17 BG BG028827A patent/BG25636A3/xx unknown
- 1974-06-18 IL IL45060A patent/IL45060A/en unknown
- 1974-06-25 JP JP49071970A patent/JPS5036636A/ja active Pending
- 1974-06-28 RO RO7479338A patent/RO69333A/ro unknown
- 1974-07-01 ZA ZA00744217A patent/ZA744217B/xx unknown
- 1974-07-01 NO NO742394A patent/NO742394L/no unknown
- 1974-07-04 NL NL7409071A patent/NL7409071A/xx not_active Application Discontinuation
- 1974-07-04 BR BR5534/74A patent/BR7405534D0/pt unknown
- 1974-07-04 FR FR7423307A patent/FR2235645B1/fr not_active Expired
- 1974-07-05 CH CH926774A patent/CH585005A5/xx not_active IP Right Cessation
- 1974-07-05 HU HUBA3109A patent/HU169820B/hu unknown
- 1974-07-05 PL PL1974172460A patent/PL94007B1/pl unknown
- 1974-07-05 CS CS744807A patent/CS189658B2/cs unknown
- 1974-07-05 DD DD179738A patent/DD111778A5/xx unknown
- 1974-07-05 LU LU70472A patent/LU70472A1/xx unknown
- 1974-07-05 SU SU7402042434A patent/SU579844A3/ru active
- 1974-07-05 BE BE146264A patent/BE817305A/xx unknown
- 1974-07-05 GB GB2987074A patent/GB1471772A/en not_active Expired
- 1974-07-05 DK DK361174A patent/DK137742C/da not_active IP Right Cessation
- 1974-07-05 IT IT51942/74A patent/IT1049296B/it active
- 1974-07-05 SE SE7408882A patent/SE7408882L/xx unknown
- 1974-07-06 ES ES428035A patent/ES428035A1/es not_active Expired
Also Published As
Publication number | Publication date |
---|---|
DD111778A5 (pl) | 1975-03-12 |
DK137742B (da) | 1978-05-01 |
IL45060A0 (en) | 1974-09-10 |
ZA744217B (en) | 1975-08-27 |
SU579844A3 (ru) | 1977-11-05 |
DE2334563A1 (de) | 1975-01-30 |
DK361174A (pl) | 1975-02-24 |
FR2235645B1 (pl) | 1978-07-07 |
DK137742C (da) | 1978-10-09 |
SE7408882L (pl) | 1975-01-08 |
GB1471772A (en) | 1977-04-27 |
BG22056A3 (pl) | 1976-11-25 |
BR7405534D0 (pt) | 1975-05-06 |
FR2235645A1 (pl) | 1975-01-31 |
NL7409071A (nl) | 1975-01-09 |
AU7028774A (en) | 1976-01-08 |
NO742394L (pl) | 1975-02-03 |
HU169820B (pl) | 1977-02-28 |
BE817305A (fr) | 1975-01-06 |
AR217032A1 (es) | 1980-02-29 |
CS189658B2 (en) | 1979-04-30 |
LU70472A1 (pl) | 1974-11-28 |
RO69333A (ro) | 1980-06-15 |
ES428035A1 (es) | 1977-02-01 |
JPS5036636A (pl) | 1975-04-05 |
CH585005A5 (pl) | 1977-02-28 |
IL45060A (en) | 1977-10-31 |
IT1049296B (it) | 1981-01-20 |
BG25636A3 (bg) | 1978-11-10 |
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RECP | Rectifications of patent specification |