PL94688B1 - Synergiczny srodek chwastobojczy - Google Patents
Synergiczny srodek chwastobojczy Download PDFInfo
- Publication number
- PL94688B1 PL94688B1 PL1973167222A PL16722273A PL94688B1 PL 94688 B1 PL94688 B1 PL 94688B1 PL 1973167222 A PL1973167222 A PL 1973167222A PL 16722273 A PL16722273 A PL 16722273A PL 94688 B1 PL94688 B1 PL 94688B1
- Authority
- PL
- Poland
- Prior art keywords
- damage
- soybean
- soil
- herbicide
- mabt
- Prior art date
Links
- 230000002195 synergetic effect Effects 0.000 title claims description 7
- 239000004009 herbicide Substances 0.000 claims description 44
- 230000002363 herbicidal effect Effects 0.000 claims description 42
- 239000004480 active ingredient Substances 0.000 claims description 12
- 244000068988 Glycine max Species 0.000 description 47
- 241000196324 Embryophyta Species 0.000 description 46
- 235000010469 Glycine max Nutrition 0.000 description 44
- 230000006378 damage Effects 0.000 description 42
- 239000003795 chemical substances by application Substances 0.000 description 32
- 239000002689 soil Substances 0.000 description 32
- 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 26
- 238000009331 sowing Methods 0.000 description 20
- 238000012360 testing method Methods 0.000 description 19
- 150000001875 compounds Chemical class 0.000 description 17
- 239000000203 mixture Substances 0.000 description 17
- 230000009467 reduction Effects 0.000 description 10
- 238000000034 method Methods 0.000 description 8
- LZGUHMNOBNWABZ-UHFFFAOYSA-N n-nitro-n-phenylnitramide Chemical compound [O-][N+](=O)N([N+]([O-])=O)C1=CC=CC=C1 LZGUHMNOBNWABZ-UHFFFAOYSA-N 0.000 description 8
- 239000013543 active substance Substances 0.000 description 6
- 230000003042 antagnostic effect Effects 0.000 description 6
- 239000004927 clay Substances 0.000 description 6
- 239000013068 control sample Substances 0.000 description 5
- 239000007921 spray Substances 0.000 description 5
- 239000003995 emulsifying agent Substances 0.000 description 4
- 239000003960 organic solvent Substances 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- 230000008653 root damage Effects 0.000 description 4
- 230000000007 visual effect Effects 0.000 description 4
- QMNWYGTWTXOQTP-UHFFFAOYSA-N 1h-triazin-6-one Chemical class O=C1C=CN=NN1 QMNWYGTWTXOQTP-UHFFFAOYSA-N 0.000 description 3
- QFUSCYRJMXLNRB-UHFFFAOYSA-N 2,6-dinitroaniline Chemical class NC1=C([N+]([O-])=O)C=CC=C1[N+]([O-])=O QFUSCYRJMXLNRB-UHFFFAOYSA-N 0.000 description 3
- 206010061217 Infestation Diseases 0.000 description 3
- 241000209504 Poaceae Species 0.000 description 3
- 230000008901 benefit Effects 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 239000004495 emulsifiable concentrate Substances 0.000 description 3
- 238000002474 experimental method Methods 0.000 description 3
- 239000005416 organic matter Substances 0.000 description 3
- 239000002245 particle Substances 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- 238000001228 spectrum Methods 0.000 description 3
- 238000005507 spraying Methods 0.000 description 3
- 239000004094 surface-active agent Substances 0.000 description 3
- ZNQVEEAIQZEUHB-UHFFFAOYSA-N 2-ethoxyethanol Chemical compound CCOCCO ZNQVEEAIQZEUHB-UHFFFAOYSA-N 0.000 description 2
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 2
- 244000062793 Sorghum vulgare Species 0.000 description 2
- 230000009471 action Effects 0.000 description 2
- 239000000969 carrier Substances 0.000 description 2
- 239000012141 concentrate Substances 0.000 description 2
- CRPOUZQWHJYTMS-UHFFFAOYSA-N dialuminum;magnesium;disilicate Chemical compound [Mg+2].[Al+3].[Al+3].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-] CRPOUZQWHJYTMS-UHFFFAOYSA-N 0.000 description 2
- 239000008187 granular material Substances 0.000 description 2
- 239000008188 pellet Substances 0.000 description 2
- 230000008654 plant damage Effects 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 230000009528 severe injury Effects 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 239000008096 xylene Substances 0.000 description 2
- CGNBQYFXGQHUQP-UHFFFAOYSA-N 2,3-dinitroaniline Chemical class NC1=CC=CC([N+]([O-])=O)=C1[N+]([O-])=O CGNBQYFXGQHUQP-UHFFFAOYSA-N 0.000 description 1
- 229940093475 2-ethoxyethanol Drugs 0.000 description 1
- 244000296912 Ageratum conyzoides Species 0.000 description 1
- 235000004405 Ageratum conyzoides Nutrition 0.000 description 1
- 239000005995 Aluminium silicate Substances 0.000 description 1
- 238000012935 Averaging Methods 0.000 description 1
- 244000056139 Brassica cretica Species 0.000 description 1
- 235000003351 Brassica cretica Nutrition 0.000 description 1
- 235000003343 Brassica rupestris Nutrition 0.000 description 1
- 241001609030 Brosme brosme Species 0.000 description 1
- 235000007516 Chrysanthemum Nutrition 0.000 description 1
- 235000008495 Chrysanthemum leucanthemum Nutrition 0.000 description 1
- 244000189548 Chrysanthemum x morifolium Species 0.000 description 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
- 241001456088 Hesperocnide Species 0.000 description 1
- 240000004153 Hibiscus sabdariffa Species 0.000 description 1
- 235000001018 Hibiscus sabdariffa Nutrition 0.000 description 1
- 240000001549 Ipomoea eriocarpa Species 0.000 description 1
- 235000005146 Ipomoea eriocarpa Nutrition 0.000 description 1
- 239000005909 Kieselgur Substances 0.000 description 1
- 235000000391 Lepidium draba Nutrition 0.000 description 1
- 241000985630 Lota lota Species 0.000 description 1
- 240000004658 Medicago sativa Species 0.000 description 1
- 235000017587 Medicago sativa ssp. sativa Nutrition 0.000 description 1
- 235000010621 Medicago sativa subsp falcata Nutrition 0.000 description 1
- 244000046070 Medicago sativa subsp falcata Species 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 108010064851 Plant Proteins Proteins 0.000 description 1
- 235000005291 Rumex acetosa Nutrition 0.000 description 1
- 244000124765 Salsola kali Species 0.000 description 1
- 235000007658 Salsola kali Nutrition 0.000 description 1
- 241000269821 Scombridae Species 0.000 description 1
- 241000232088 Setaria <nematode> Species 0.000 description 1
- 235000008515 Setaria glauca Nutrition 0.000 description 1
- 235000001155 Setaria leucopila Nutrition 0.000 description 1
- 244000010062 Setaria pumila Species 0.000 description 1
- 240000003461 Setaria viridis Species 0.000 description 1
- 235000002248 Setaria viridis Nutrition 0.000 description 1
- 235000010086 Setaria viridis var. viridis Nutrition 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 235000000342 Solanum rostratum Nutrition 0.000 description 1
- 241000193264 Solanum rostratum Species 0.000 description 1
- 235000011684 Sorghum saccharatum Nutrition 0.000 description 1
- 108010073771 Soybean Proteins Proteins 0.000 description 1
- 241000269841 Thunnus albacares Species 0.000 description 1
- 235000009108 Urtica dioica Nutrition 0.000 description 1
- 241001148683 Zostera marina Species 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 150000004996 alkyl benzenes Chemical class 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- -1 aralkyl sulfonate salts Chemical class 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 230000004071 biological effect Effects 0.000 description 1
- QKSKPIVNLNLAAV-UHFFFAOYSA-N bis(2-chloroethyl) sulfide Chemical compound ClCCSCCCl QKSKPIVNLNLAAV-UHFFFAOYSA-N 0.000 description 1
- 239000008280 blood Substances 0.000 description 1
- 210000004369 blood Anatomy 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 235000013339 cereals Nutrition 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 230000000295 complement effect Effects 0.000 description 1
- 239000010779 crude oil Substances 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 230000018109 developmental process 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
- 230000003292 diminished effect Effects 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 230000001804 emulsifying effect Effects 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 238000009313 farming Methods 0.000 description 1
- 230000035784 germination Effects 0.000 description 1
- 238000003306 harvesting Methods 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 239000004615 ingredient Substances 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
- 230000003902 lesion Effects 0.000 description 1
- 229920005610 lignin Polymers 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 235000020640 mackerel Nutrition 0.000 description 1
- 235000019713 millet Nutrition 0.000 description 1
- 230000009526 moderate injury Effects 0.000 description 1
- 229910052901 montmorillonite Inorganic materials 0.000 description 1
- 235000010460 mustard Nutrition 0.000 description 1
- RZSCFTDHFNHMOR-UHFFFAOYSA-N n-(2,4-difluorophenyl)-2-[3-(trifluoromethyl)phenoxy]pyridine-3-carboxamide;1,1-dimethyl-3-(4-propan-2-ylphenyl)urea Chemical compound CC(C)C1=CC=C(NC(=O)N(C)C)C=C1.FC1=CC(F)=CC=C1NC(=O)C1=CC=CN=C1OC1=CC=CC(C(F)(F)F)=C1 RZSCFTDHFNHMOR-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
- 235000015097 nutrients Nutrition 0.000 description 1
- 235000016709 nutrition Nutrition 0.000 description 1
- 230000035764 nutrition Effects 0.000 description 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
- 239000004482 other powder Substances 0.000 description 1
- VSXGXPNADZQTGQ-UHFFFAOYSA-N oxirane;phenol Chemical class C1CO1.OC1=CC=CC=C1 VSXGXPNADZQTGQ-UHFFFAOYSA-N 0.000 description 1
- 239000000575 pesticide Substances 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 231100000208 phytotoxic Toxicity 0.000 description 1
- 230000000885 phytotoxic effect Effects 0.000 description 1
- 235000021118 plant-derived protein Nutrition 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 235000021067 refined food Nutrition 0.000 description 1
- 230000007226 seed germination Effects 0.000 description 1
- 235000003513 sheep sorrel Nutrition 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- 235000019710 soybean protein Nutrition 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 238000005563 spheronization Methods 0.000 description 1
- 125000001273 sulfonato group Chemical group [O-]S(*)(=O)=O 0.000 description 1
- 239000013589 supplement Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 239000012747 synergistic agent Substances 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 239000004563 wettable powder Substances 0.000 description 1
- 150000003738 xylenes Chemical class 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D253/00—Heterocyclic compounds containing six-membered rings having three nitrogen atoms as the only ring hetero atoms, not provided for by group C07D251/00
- C07D253/02—Heterocyclic compounds containing six-membered rings having three nitrogen atoms as the only ring hetero atoms, not provided for by group C07D251/00 not condensed with other rings
- C07D253/06—1,2,4-Triazines
-
- 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
- A01N43/707—1,2,3- or 1,2,4-triazines; Hydrogenated 1,2,3- or 1,2,4-triazines
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)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US31392172A | 1972-12-11 | 1972-12-11 |
Publications (1)
Publication Number | Publication Date |
---|---|
PL94688B1 true PL94688B1 (pl) | 1977-08-31 |
Family
ID=23217762
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PL1973167222A PL94688B1 (pl) | 1972-12-11 | 1973-12-11 | Synergiczny srodek chwastobojczy |
Country Status (27)
Families Citing this family (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4192670A (en) * | 1974-10-15 | 1980-03-11 | Eli Lilly And Company | Acetal derivatives of 4-(substituted amino)-3,5-dinitrobenzaldehydes |
GB1598765A (en) * | 1977-06-27 | 1981-09-23 | Lilly Co Eli | N-alkoxydinitro anilines and their herbicidal compositions |
US4087460A (en) * | 1977-06-27 | 1978-05-02 | Eli Lilly And Company | Substituted N-alkoxy-N-substituted-2,6-dinitroanilines and intermediates for the preparation thereof |
US4150968A (en) * | 1978-02-01 | 1979-04-24 | Mobay Chemical Corporation | Emulsifiable liquid concentrates containing 4-amino-6-t-butyl-3-(methylthio)-1,2,4-triazin-5-one and 2-chloro-N-(2,6-diethylphenyl)-N-methoxymethylacetamide |
US4699646A (en) * | 1981-06-11 | 1987-10-13 | American Cyanamid Co. | Dinitroaniline yield enhancing agents for legumes |
WO2011082954A2 (de) * | 2009-12-17 | 2011-07-14 | Bayer Cropscience Ag | Herbizide mittel enthaltend flufenacet |
WO2017220308A1 (en) | 2016-06-20 | 2017-12-28 | Basf Se | Powders and granules and process for making such powders and granules |
-
1973
- 1973-12-04 ZA ZA00739198A patent/ZA739198B/xx unknown
- 1973-12-06 AU AU63346/73A patent/AU472903B2/en not_active Expired
- 1973-12-07 BE BE1005571A patent/BE808343A/xx unknown
- 1973-12-10 SU SU1978802A patent/SU493949A3/ru active
- 1973-12-10 SE SE7316655A patent/SE393919B/xx unknown
- 1973-12-10 HU HUEI513A patent/HU169865B/hu unknown
- 1973-12-10 BR BR9677/73A patent/BR7309677D0/pt unknown
- 1973-12-10 IL IL43793A patent/IL43793A/en unknown
- 1973-12-10 DE DE2361463A patent/DE2361463A1/de not_active Withdrawn
- 1973-12-10 DK DK668773AA patent/DK133362B/da unknown
- 1973-12-10 GB GB5723173A patent/GB1460304A/en not_active Expired
- 1973-12-11 AT AT1034673A patent/AT328216B/de not_active IP Right Cessation
- 1973-12-11 CH CH1733773A patent/CH585004A5/xx not_active IP Right Cessation
- 1973-12-11 NL NL7316967A patent/NL7316967A/xx not_active Application Discontinuation
- 1973-12-11 RO RO7300076952A patent/RO62673A/ro unknown
- 1973-12-11 JP JP13853873A patent/JPS5647161B2/ja not_active Expired
- 1973-12-11 DD DD175255A patent/DD109497A5/xx unknown
- 1973-12-11 AR AR251448A patent/AR202198A1/es active
- 1973-12-11 PL PL1973167222A patent/PL94688B1/pl unknown
- 1973-12-11 BG BG25213A patent/BG20750A3/xx unknown
- 1973-12-11 CS CS738565A patent/CS189619B2/cs unknown
- 1973-12-11 OA OA55080A patent/OA04578A/xx unknown
- 1973-12-11 IE IE2237/73A patent/IE38628B1/xx unknown
- 1973-12-11 FR FR7344096A patent/FR2209510B1/fr not_active Expired
- 1973-12-12 MW MW69/73*UA patent/MW6973A1/xx unknown
- 1973-12-20 IT IT3549/73A patent/IT1060104B/it active
- 1973-12-28 ZM ZM203/73A patent/ZM20373A1/xx unknown
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