CH510384A - Herbizides Gemisch und dessen Anwendung - Google Patents
Herbizides Gemisch und dessen AnwendungInfo
- Publication number
- CH510384A CH510384A CH1161569A CH1161569A CH510384A CH 510384 A CH510384 A CH 510384A CH 1161569 A CH1161569 A CH 1161569A CH 1161569 A CH1161569 A CH 1161569A CH 510384 A CH510384 A CH 510384A
- Authority
- CH
- Switzerland
- Prior art keywords
- sep
- methyl
- ester
- acid
- herbicidal
- Prior art date
Links
- 230000002363 herbicidal effect Effects 0.000 title claims description 35
- 239000000203 mixture Substances 0.000 title claims description 20
- 241000209094 Oryza Species 0.000 claims description 32
- 241000196324 Embryophyta Species 0.000 claims description 24
- 239000004009 herbicide Substances 0.000 claims description 22
- 150000001875 compounds Chemical class 0.000 claims description 21
- 235000007164 Oryza sativa Nutrition 0.000 claims description 18
- 235000009566 rice Nutrition 0.000 claims description 18
- 150000002148 esters Chemical class 0.000 claims description 15
- 239000002253 acid Substances 0.000 claims description 14
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 13
- -1 2,4-dichloro-6-fluorophenyl-4-nitrophenyl ether 4,6-bis (ethylamino) -2-methylthio-1,3,5-triazine Chemical compound 0.000 claims description 12
- 239000004480 active ingredient Substances 0.000 claims description 11
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 9
- XITQUSLLOSKDTB-UHFFFAOYSA-N nitrofen Chemical compound C1=CC([N+](=O)[O-])=CC=C1OC1=CC=C(Cl)C=C1Cl XITQUSLLOSKDTB-UHFFFAOYSA-N 0.000 claims description 5
- RRWGAOYVBOKACL-UHFFFAOYSA-N 1,3,5-trichloro-2-[5-nitro-2-[4-nitro-2-(2,4,6-trichlorophenyl)phenoxy]phenyl]benzene Chemical compound ClC=1C=C(Cl)C=C(Cl)C=1C1=CC([N+](=O)[O-])=CC=C1OC1=CC=C([N+]([O-])=O)C=C1C1=C(Cl)C=C(Cl)C=C1Cl RRWGAOYVBOKACL-UHFFFAOYSA-N 0.000 claims description 4
- 125000000066 S-methyl group Chemical group [H]C([H])([H])S* 0.000 claims description 4
- 239000003795 chemical substances by application Substances 0.000 claims description 3
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 2
- 229910052760 oxygen Inorganic materials 0.000 claims description 2
- 239000001301 oxygen Substances 0.000 claims description 2
- 229910052717 sulfur Inorganic materials 0.000 claims description 2
- 239000011593 sulfur Substances 0.000 claims description 2
- FIDRAVVQGKNYQK-UHFFFAOYSA-N 1,2,3,4-tetrahydrotriazine Chemical compound C1NNNC=C1 FIDRAVVQGKNYQK-UHFFFAOYSA-N 0.000 claims 1
- OELWFMFENYNUQY-UHFFFAOYSA-N 2-(4-chloro-2-methylphenoxy)ethanethioic s-acid Chemical compound CC1=CC(Cl)=CC=C1OCC(S)=O OELWFMFENYNUQY-UHFFFAOYSA-N 0.000 claims 1
- DEKIOXLBNIFKSO-UHFFFAOYSA-N 2-n,4-n-diethyl-6-methylsulfanyl-1,3,5-triazine-2,4-diamine;6-methylsulfanyl-2-n,4-n-di(propan-2-yl)-1,3,5-triazine-2,4-diamine Chemical compound CCNC1=NC(NCC)=NC(SC)=N1.CSC1=NC(NC(C)C)=NC(NC(C)C)=N1 DEKIOXLBNIFKSO-UHFFFAOYSA-N 0.000 claims 1
- 229930045534 Me ester-Cyclohexaneundecanoic acid Natural products 0.000 claims 1
- 230000001419 dependent effect Effects 0.000 claims 1
- 241000759199 Eleocharis acicularis Species 0.000 description 18
- 240000000178 Monochoria vaginalis Species 0.000 description 14
- PQFIWRBUKOZHMI-UHFFFAOYSA-N s-methyl 2-(4-chloro-2-methylphenoxy)ethanethioate Chemical compound CSC(=O)COC1=CC=C(Cl)C=C1C PQFIWRBUKOZHMI-UHFFFAOYSA-N 0.000 description 10
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 10
- 230000000694 effects Effects 0.000 description 9
- 239000012141 concentrate Substances 0.000 description 8
- 238000002474 experimental method Methods 0.000 description 8
- 230000009931 harmful effect Effects 0.000 description 8
- 239000008187 granular material Substances 0.000 description 7
- 238000012360 testing method Methods 0.000 description 7
- 244000088461 Panicum crus-galli Species 0.000 description 6
- 235000011999 Panicum crusgalli Nutrition 0.000 description 6
- 239000000839 emulsion Substances 0.000 description 6
- 239000004615 ingredient Substances 0.000 description 5
- 238000000034 method Methods 0.000 description 5
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
- AZFKQCNGMSSWDS-UHFFFAOYSA-N MCPA-thioethyl Chemical compound CCSC(=O)COC1=CC=C(Cl)C=C1C AZFKQCNGMSSWDS-UHFFFAOYSA-N 0.000 description 4
- 239000000470 constituent Substances 0.000 description 4
- 238000007865 diluting Methods 0.000 description 4
- AAEVYOVXGOFMJO-UHFFFAOYSA-N prometryn Chemical compound CSC1=NC(NC(C)C)=NC(NC(C)C)=N1 AAEVYOVXGOFMJO-UHFFFAOYSA-N 0.000 description 4
- MGLWZSOBALDPEK-UHFFFAOYSA-N simetryn Chemical compound CCNC1=NC(NCC)=NC(SC)=N1 MGLWZSOBALDPEK-UHFFFAOYSA-N 0.000 description 4
- SHLIYHXMYSXWAG-UHFFFAOYSA-N O-methyl 2-(4-chloro-2-methylphenoxy)ethanethioate Chemical compound COC(COC1=C(C=C(C=C1)Cl)C)=S SHLIYHXMYSXWAG-UHFFFAOYSA-N 0.000 description 3
- XCHKGEWYMWKALV-UHFFFAOYSA-N o-ethyl 2-(4-chloro-2-methylphenoxy)ethanethioate Chemical compound CCOC(=S)COC1=CC=C(Cl)C=C1C XCHKGEWYMWKALV-UHFFFAOYSA-N 0.000 description 3
- 239000002689 soil Substances 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- 230000002195 synergetic effect Effects 0.000 description 3
- WTVIMCPPMFOGHF-UHFFFAOYSA-N 2-(4-chloro-2-methylphenoxy)acetonitrile Chemical compound CC1=CC(Cl)=CC=C1OCC#N WTVIMCPPMFOGHF-UHFFFAOYSA-N 0.000 description 2
- 241000817048 Cyperus microiria Species 0.000 description 2
- 241000721671 Ludwigia Species 0.000 description 2
- 244000081171 Ludwigia prostrata Species 0.000 description 2
- LSDPWZHWYPCBBB-UHFFFAOYSA-N Methanethiol Chemical compound SC LSDPWZHWYPCBBB-UHFFFAOYSA-N 0.000 description 2
- 239000000440 bentonite Substances 0.000 description 2
- 229910000278 bentonite Inorganic materials 0.000 description 2
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 2
- 235000013339 cereals Nutrition 0.000 description 2
- 239000013078 crystal Substances 0.000 description 2
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
- GVGUFUZHNYFZLC-UHFFFAOYSA-N dodecyl benzenesulfonate;sodium Chemical compound [Na].CCCCCCCCCCCCOS(=O)(=O)C1=CC=CC=C1 GVGUFUZHNYFZLC-UHFFFAOYSA-N 0.000 description 2
- 238000011835 investigation Methods 0.000 description 2
- 230000002262 irrigation Effects 0.000 description 2
- 238000003973 irrigation Methods 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 229940080264 sodium dodecylbenzenesulfonate Drugs 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- MVHWKYHDYCGNQN-UHFFFAOYSA-N 1,5-dichloro-3-fluoro-2-(4-nitrophenoxy)benzene Chemical compound C1=CC([N+](=O)[O-])=CC=C1OC1=C(F)C=C(Cl)C=C1Cl MVHWKYHDYCGNQN-UHFFFAOYSA-N 0.000 description 1
- OVSKIKFHRZPJSS-DOMIDYPGSA-N 2-(2,4-dichlorophenoxy)acetic acid Chemical compound OC(=O)[14CH2]OC1=CC=C(Cl)C=C1Cl OVSKIKFHRZPJSS-DOMIDYPGSA-N 0.000 description 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
- 241000234653 Cyperus Species 0.000 description 1
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical compound S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- 240000004428 Lindernia procumbens Species 0.000 description 1
- 239000005574 MCPA Substances 0.000 description 1
- 241000169139 Monochoria Species 0.000 description 1
- 235000003990 Monochoria hastata Nutrition 0.000 description 1
- 241000877993 Potamogeton distinctus Species 0.000 description 1
- APTGPWJUOYMUCE-UHFFFAOYSA-N S-Ethyl thioacetate Chemical compound CCSC(C)=O APTGPWJUOYMUCE-UHFFFAOYSA-N 0.000 description 1
- 241001408202 Sagittaria pygmaea Species 0.000 description 1
- WHKUVVPPKQRRBV-UHFFFAOYSA-N Trasan Chemical compound CC1=CC(Cl)=CC=C1OCC(O)=O WHKUVVPPKQRRBV-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 239000000443 aerosol Substances 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 239000002775 capsule Substances 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 239000002361 compost Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 230000001066 destructive effect Effects 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 230000008029 eradication Effects 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 210000003608 fece Anatomy 0.000 description 1
- 230000035784 germination Effects 0.000 description 1
- 230000009036 growth inhibition Effects 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- 229910000037 hydrogen sulfide Inorganic materials 0.000 description 1
- 238000004898 kneading Methods 0.000 description 1
- 239000010410 layer Substances 0.000 description 1
- 239000010871 livestock manure Substances 0.000 description 1
- OSDZHDOKXGSWOD-UHFFFAOYSA-N nitroxyl;hydrochloride Chemical compound Cl.O=N OSDZHDOKXGSWOD-UHFFFAOYSA-N 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 230000003449 preventive effect Effects 0.000 description 1
- 230000002062 proliferating effect Effects 0.000 description 1
- 230000035755 proliferation Effects 0.000 description 1
- 230000001850 reproductive effect Effects 0.000 description 1
- 230000005070 ripening Effects 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- YWFDLYNAGWTSSN-UHFFFAOYSA-N sulfanylideneazanium chloride Chemical compound Cl.N=S YWFDLYNAGWTSSN-UHFFFAOYSA-N 0.000 description 1
- 239000002344 surface layer Substances 0.000 description 1
- 239000012085 test solution Substances 0.000 description 1
- 238000002054 transplantation Methods 0.000 description 1
- 239000004563 wettable powder 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
- A01N39/00—Biocides, pest repellants or attractants, or plant growth regulators containing aryloxy- or arylthio-aliphatic or cycloaliphatic compounds, containing the group or, e.g. phenoxyethylamine, phenylthio-acetonitrile, phenoxyacetone
-
- 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
- A01N39/00—Biocides, pest repellants or attractants, or plant growth regulators containing aryloxy- or arylthio-aliphatic or cycloaliphatic compounds, containing the group or, e.g. phenoxyethylamine, phenylthio-acetonitrile, phenoxyacetone
- A01N39/02—Aryloxy-carboxylic acids; Derivatives thereof
- A01N39/04—Aryloxy-acetic acids; Derivatives thereof
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)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP5359268 | 1968-07-31 | ||
JP5761668 | 1968-08-15 | ||
JP5761768 | 1968-08-15 | ||
JP5507369 | 1969-07-14 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH510384A true CH510384A (de) | 1971-07-31 |
Family
ID=27462926
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH1161569A CH510384A (de) | 1968-07-31 | 1969-07-30 | Herbizides Gemisch und dessen Anwendung |
Country Status (4)
Country | Link |
---|---|
CH (1) | CH510384A (enrdf_load_stackoverflow) |
DE (2) | DE1939010C3 (enrdf_load_stackoverflow) |
GB (1) | GB1263169A (enrdf_load_stackoverflow) |
NL (1) | NL169024C (enrdf_load_stackoverflow) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE3304204A1 (de) * | 1983-02-08 | 1984-08-09 | Bayer Ag, 5090 Leverkusen | Substituierte alkanthiocarbonsaeure-derivate |
-
1969
- 1969-07-24 GB GB3735169A patent/GB1263169A/en not_active Expired
- 1969-07-30 CH CH1161569A patent/CH510384A/de not_active IP Right Cessation
- 1969-07-31 DE DE19691939010 patent/DE1939010C3/de not_active Expired
- 1969-07-31 NL NL6911679A patent/NL169024C/xx not_active IP Right Cessation
- 1969-07-31 DE DE19691966665 patent/DE1966665B2/de active Granted
Also Published As
Publication number | Publication date |
---|---|
DE1966665A1 (de) | 1973-08-23 |
GB1263169A (en) | 1972-02-09 |
DE1939010A1 (de) | 1970-07-16 |
DE1939010B2 (de) | 1973-10-04 |
NL169024C (nl) | 1982-06-01 |
DE1939010C3 (de) | 1974-05-16 |
DE1966665B2 (de) | 1977-02-17 |
NL169024B (nl) | 1982-01-04 |
NL6911679A (enrdf_load_stackoverflow) | 1970-02-03 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
PL | Patent ceased |