CS266572B2 - Selective herbicide with antidote content - Google Patents
Selective herbicide with antidote content Download PDFInfo
- Publication number
- CS266572B2 CS266572B2 CS857399A CS739985A CS266572B2 CS 266572 B2 CS266572 B2 CS 266572B2 CS 857399 A CS857399 A CS 857399A CS 739985 A CS739985 A CS 739985A CS 266572 B2 CS266572 B2 CS 266572B2
- Authority
- CS
- Czechoslovakia
- Prior art keywords
- antidote
- weeds
- herbicides
- eptc
- acetochlor
- Prior art date
Links
- 230000002363 herbicidal effect Effects 0.000 title claims description 38
- 239000000729 antidote Substances 0.000 title claims description 32
- 239000004009 herbicide Substances 0.000 title description 34
- 239000000203 mixture Substances 0.000 claims description 41
- VONWPEXRCLHKRJ-UHFFFAOYSA-N 2-chloro-n-phenylacetamide Chemical class ClCC(=O)NC1=CC=CC=C1 VONWPEXRCLHKRJ-UHFFFAOYSA-N 0.000 claims description 9
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 claims description 6
- 239000007788 liquid Substances 0.000 claims description 6
- 239000002904 solvent Substances 0.000 claims description 6
- 239000008096 xylene Substances 0.000 claims description 6
- 239000003085 diluting agent Substances 0.000 claims description 4
- 239000002736 nonionic surfactant Substances 0.000 claims description 4
- 239000004094 surface-active agent Substances 0.000 claims description 4
- 239000002563 ionic surfactant Substances 0.000 claims description 3
- 241000196324 Embryophyta Species 0.000 description 46
- OHXLAOJLJWLEIP-UHFFFAOYSA-N 2-(dichloromethyl)-2-methyl-1,3-dioxolane Chemical compound ClC(Cl)C1(C)OCCO1 OHXLAOJLJWLEIP-UHFFFAOYSA-N 0.000 description 28
- 240000008042 Zea mays Species 0.000 description 25
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 25
- GUVLYNGULCJVDO-UHFFFAOYSA-N EPTC Chemical compound CCCN(CCC)C(=O)SCC GUVLYNGULCJVDO-UHFFFAOYSA-N 0.000 description 20
- 239000002689 soil Substances 0.000 description 20
- VTNQPKFIQCLBDU-UHFFFAOYSA-N Acetochlor Chemical compound CCOCN(C(=O)CCl)C1=C(C)C=CC=C1CC VTNQPKFIQCLBDU-UHFFFAOYSA-N 0.000 description 19
- XCSGPAVHZFQHGE-UHFFFAOYSA-N alachlor Chemical compound CCC1=CC=CC(CC)=C1N(COC)C(=O)CCl XCSGPAVHZFQHGE-UHFFFAOYSA-N 0.000 description 19
- BMTAFVWTTFSTOG-UHFFFAOYSA-N Butylate Chemical compound CCSC(=O)N(CC(C)C)CC(C)C BMTAFVWTTFSTOG-UHFFFAOYSA-N 0.000 description 18
- 235000016383 Zea mays subsp huehuetenangensis Nutrition 0.000 description 15
- 235000009973 maize Nutrition 0.000 description 15
- 231100000674 Phytotoxicity Toxicity 0.000 description 14
- 238000012360 testing method Methods 0.000 description 14
- 230000000694 effects Effects 0.000 description 11
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 10
- 229940075522 antidotes Drugs 0.000 description 10
- MXWJVTOOROXGIU-UHFFFAOYSA-N atrazine Chemical compound CCNC1=NC(Cl)=NC(NC(C)C)=N1 MXWJVTOOROXGIU-UHFFFAOYSA-N 0.000 description 10
- 235000005822 corn Nutrition 0.000 description 10
- 239000003795 chemical substances by application Substances 0.000 description 9
- 244000237956 Amaranthus retroflexus Species 0.000 description 8
- 235000013479 Amaranthus retroflexus Nutrition 0.000 description 8
- 238000002474 experimental method Methods 0.000 description 8
- 208000024891 symptom Diseases 0.000 description 8
- 244000038559 crop plants Species 0.000 description 7
- 230000006378 damage Effects 0.000 description 7
- 239000004480 active ingredient Substances 0.000 description 6
- 239000000839 emulsion Substances 0.000 description 6
- 238000000034 method Methods 0.000 description 6
- 238000001556 precipitation Methods 0.000 description 6
- 241000219318 Amaranthus Species 0.000 description 5
- 125000004432 carbon atom Chemical group C* 0.000 description 5
- 150000001875 compounds Chemical class 0.000 description 5
- MFOUDYKPLGXPGO-UHFFFAOYSA-N propachlor Chemical compound ClCC(=O)N(C(C)C)C1=CC=CC=C1 MFOUDYKPLGXPGO-UHFFFAOYSA-N 0.000 description 5
- 239000000126 substance Substances 0.000 description 5
- NLYNUTMZTCLNOO-UHFFFAOYSA-N Chlorbromuron Chemical compound CON(C)C(=O)NC1=CC=C(Br)C(Cl)=C1 NLYNUTMZTCLNOO-UHFFFAOYSA-N 0.000 description 4
- 241000209510 Liliopsida Species 0.000 description 4
- 125000000217 alkyl group Chemical group 0.000 description 4
- 239000004495 emulsifiable concentrate Substances 0.000 description 4
- 238000011156 evaluation Methods 0.000 description 4
- 238000002360 preparation method Methods 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
- 241000219312 Chenopodium Species 0.000 description 3
- 235000009344 Chenopodium album Nutrition 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- 239000013543 active substance Substances 0.000 description 3
- -1 aliphatic alcohols Chemical class 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 239000004927 clay Substances 0.000 description 3
- 239000000084 colloidal system Substances 0.000 description 3
- 241001233957 eudicotyledons Species 0.000 description 3
- ZBJVLWIYKOAYQH-UHFFFAOYSA-N naphthalen-2-yl 2-hydroxybenzoate Chemical compound OC1=CC=CC=C1C(=O)OC1=CC=C(C=CC=C2)C2=C1 ZBJVLWIYKOAYQH-UHFFFAOYSA-N 0.000 description 3
- 238000009331 sowing Methods 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- WNXJIVFYUVYPPR-UHFFFAOYSA-N 1,3-dioxolane Chemical compound C1COCO1 WNXJIVFYUVYPPR-UHFFFAOYSA-N 0.000 description 2
- 235000004135 Amaranthus viridis Nutrition 0.000 description 2
- 240000006122 Chenopodium album Species 0.000 description 2
- 235000005484 Chenopodium berlandieri Nutrition 0.000 description 2
- 235000009332 Chenopodium rubrum Nutrition 0.000 description 2
- FZERHIULMFGESH-UHFFFAOYSA-N N-phenylacetamide Chemical compound CC(=O)NC1=CC=CC=C1 FZERHIULMFGESH-UHFFFAOYSA-N 0.000 description 2
- 244000115721 Pennisetum typhoides Species 0.000 description 2
- 235000007195 Pennisetum typhoides Nutrition 0.000 description 2
- 241000719029 Polla Species 0.000 description 2
- 235000008515 Setaria glauca Nutrition 0.000 description 2
- 240000003461 Setaria viridis Species 0.000 description 2
- 235000002248 Setaria viridis Nutrition 0.000 description 2
- 240000002439 Sorghum halepense Species 0.000 description 2
- 244000062793 Sorghum vulgare Species 0.000 description 2
- IWEDIXLBFLAXBO-UHFFFAOYSA-N dicamba Chemical compound COC1=C(Cl)C=CC(Cl)=C1C(O)=O IWEDIXLBFLAXBO-UHFFFAOYSA-N 0.000 description 2
- 125000004772 dichloromethyl group Chemical group [H]C(Cl)(Cl)* 0.000 description 2
- 239000003995 emulsifying agent Substances 0.000 description 2
- 125000005745 ethoxymethyl group Chemical group [H]C([H])([H])C([H])([H])OC([H])([H])* 0.000 description 2
- XXOYNJXVWVNOOJ-UHFFFAOYSA-N fenuron Chemical compound CN(C)C(=O)NC1=CC=CC=C1 XXOYNJXVWVNOOJ-UHFFFAOYSA-N 0.000 description 2
- 239000003864 humus Substances 0.000 description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 2
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 2
- 125000004184 methoxymethyl group Chemical group [H]C([H])([H])OC([H])([H])* 0.000 description 2
- 230000000885 phytotoxic effect Effects 0.000 description 2
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- 230000009528 severe injury Effects 0.000 description 2
- 239000007921 spray Substances 0.000 description 2
- 238000005507 spraying Methods 0.000 description 2
- 150000003918 triazines Chemical class 0.000 description 2
- FTLBMFBCTKEIRK-UHFFFAOYSA-N 4-chloro-1-N,2-N-diethyl-2H-1,3,5-triazine-1,2-diamine Chemical compound ClC=1N=CN(C(N1)NCC)NCC FTLBMFBCTKEIRK-UHFFFAOYSA-N 0.000 description 1
- 235000006760 Acer pensylvanicum Nutrition 0.000 description 1
- 241000561747 Amaranthus albus Species 0.000 description 1
- 235000015363 Amaranthus cruentus Nutrition 0.000 description 1
- 240000006273 Amaranthus graecizans Species 0.000 description 1
- 244000300297 Amaranthus hybridus Species 0.000 description 1
- 235000008427 Brassica arvensis Nutrition 0.000 description 1
- 244000056139 Brassica cretica Species 0.000 description 1
- 235000003351 Brassica cretica Nutrition 0.000 description 1
- 244000024671 Brassica kaber Species 0.000 description 1
- 235000003343 Brassica rupestris Nutrition 0.000 description 1
- 235000004977 Brassica sinapistrum Nutrition 0.000 description 1
- 208000003643 Callosities Diseases 0.000 description 1
- 244000025254 Cannabis sativa Species 0.000 description 1
- 240000001579 Cirsium arvense Species 0.000 description 1
- 239000005504 Dicamba Substances 0.000 description 1
- 244000058871 Echinochloa crus-galli Species 0.000 description 1
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 1
- 244000060234 Gmelina philippensis Species 0.000 description 1
- 235000005206 Hibiscus Nutrition 0.000 description 1
- 235000007185 Hibiscus lunariifolius Nutrition 0.000 description 1
- 244000284380 Hibiscus rosa sinensis Species 0.000 description 1
- 241001075721 Hibiscus trionum Species 0.000 description 1
- 235000001047 Hibiscus trionum Nutrition 0.000 description 1
- 206010020649 Hyperkeratosis Diseases 0.000 description 1
- 244000237786 Lathyrus tuberosus Species 0.000 description 1
- 235000007252 Lathyrus tuberosus Nutrition 0.000 description 1
- 241000221024 Mercurialis Species 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 241000209117 Panicum Species 0.000 description 1
- 235000011999 Panicum crusgalli Nutrition 0.000 description 1
- 240000008114 Panicum miliaceum Species 0.000 description 1
- 235000007199 Panicum miliaceum Nutrition 0.000 description 1
- 235000006443 Panicum miliaceum subsp. miliaceum Nutrition 0.000 description 1
- 235000009037 Panicum miliaceum subsp. ruderale Nutrition 0.000 description 1
- 241000286209 Phasianidae Species 0.000 description 1
- 241001167724 Reseda lutea Species 0.000 description 1
- 235000011684 Sorghum saccharatum Nutrition 0.000 description 1
- 241000573562 Stachys pubescens Species 0.000 description 1
- 241001148683 Zostera marina Species 0.000 description 1
- 229960001413 acetanilide Drugs 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000003849 aromatic solvent Substances 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
- 235000013877 carbamide Nutrition 0.000 description 1
- 239000013043 chemical agent Substances 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 239000006184 cosolvent Substances 0.000 description 1
- 230000007812 deficiency Effects 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 150000004862 dioxolanes Chemical class 0.000 description 1
- 230000008030 elimination Effects 0.000 description 1
- 238000003379 elimination reaction Methods 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 150000002191 fatty alcohols Chemical class 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 150000002314 glycerols Polymers 0.000 description 1
- 230000009931 harmful effect Effects 0.000 description 1
- 235000019713 millet Nutrition 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 238000009343 monoculture Methods 0.000 description 1
- 235000010460 mustard Nutrition 0.000 description 1
- 239000011368 organic material Substances 0.000 description 1
- 239000005416 organic matter Substances 0.000 description 1
- 235000021317 phosphate Nutrition 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 239000004476 plant protection product Substances 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000011814 protection agent Substances 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 238000013112 stability test Methods 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 230000001052 transient effect Effects 0.000 description 1
- 150000003672 ureas Chemical class 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil 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
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
- A01N47/10—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof
- A01N47/12—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof containing a —O—CO—N< group, or a thio analogue thereof, neither directly attached to a ring nor the nitrogen atom being a member of a heterocyclic 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)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| HU387984A HU194685B (en) | 1984-10-17 | 1984-10-17 | Selective herbicide comprising chloracetanilide and thiolcarbamate derivatives as herbicidal active substance and dioxolane derivative as antidote |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CS739985A2 CS739985A2 (en) | 1989-04-14 |
| CS266572B2 true CS266572B2 (en) | 1990-01-12 |
Family
ID=10965893
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CS857399A CS266572B2 (en) | 1984-10-17 | 1985-10-17 | Selective herbicide with antidote content |
Country Status (10)
| Country | Link |
|---|---|
| EP (1) | EP0198870B1 (en, 2012) |
| CN (1) | CN1008506B (en, 2012) |
| BG (1) | BG48803A3 (en, 2012) |
| BR (1) | BR8506994A (en, 2012) |
| CS (1) | CS266572B2 (en, 2012) |
| DE (1) | DE3578305D1 (en, 2012) |
| ES (1) | ES8700013A1 (en, 2012) |
| GR (1) | GR852508B (en, 2012) |
| HU (1) | HU194685B (en, 2012) |
| WO (1) | WO1986002237A1 (en, 2012) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4664699A (en) * | 1985-02-07 | 1987-05-12 | Stauffer Chemical Company | Method of improving residual herbicidal activity and compositions |
| US5527762A (en) * | 1990-12-12 | 1996-06-18 | Zeneca Limited | Antidoting herbicidal 3-isoxazolidinone compounds |
| US5395816A (en) * | 1990-12-12 | 1995-03-07 | Imperial Chemical Industries Plc | Antidoting herbicidal 3-ixoxazolidinone compounds |
| CN100378208C (zh) * | 2006-03-03 | 2008-04-02 | 中国科学院长春应用化学研究所 | 一种水煤浆 |
| CN100447222C (zh) * | 2006-09-21 | 2008-12-31 | 太原理工大学 | 一种煤沥青水浆及其制备方法 |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NL282741A (en, 2012) * | 1961-08-31 | |||
| US4415353A (en) * | 1971-04-16 | 1983-11-15 | Stauffer Chemical Company | Herbicide compositions |
| GR71993B (en, 2012) * | 1980-11-19 | 1983-08-26 | Stavffer Chemical Company |
-
1984
- 1984-10-17 HU HU387984A patent/HU194685B/hu not_active IP Right Cessation
-
1985
- 1985-10-08 WO PCT/HU1985/000059 patent/WO1986002237A1/en active IP Right Grant
- 1985-10-08 BR BR8506994A patent/BR8506994A/pt unknown
- 1985-10-08 DE DE8585905099T patent/DE3578305D1/de not_active Expired - Fee Related
- 1985-10-08 EP EP85905099A patent/EP0198870B1/en not_active Expired - Lifetime
- 1985-10-16 GR GR852508A patent/GR852508B/el unknown
- 1985-10-16 CN CN 85108224 patent/CN1008506B/zh not_active Expired
- 1985-10-17 CS CS857399A patent/CS266572B2/cs unknown
- 1985-10-17 ES ES547977A patent/ES8700013A1/es not_active Expired
-
1986
- 1986-06-17 BG BG075387A patent/BG48803A3/xx unknown
Also Published As
| Publication number | Publication date |
|---|---|
| GR852508B (en, 2012) | 1986-02-18 |
| BG48803A3 (en) | 1991-05-15 |
| CN85108224A (zh) | 1986-07-30 |
| DE3578305D1 (de) | 1990-07-26 |
| HUT39566A (en) | 1986-10-29 |
| ES8700013A1 (es) | 1986-10-01 |
| ES547977A0 (es) | 1986-10-01 |
| BR8506994A (pt) | 1987-01-06 |
| WO1986002237A1 (en) | 1986-04-24 |
| EP0198870B1 (en) | 1990-06-20 |
| EP0198870A1 (en) | 1986-10-29 |
| HU194685B (en) | 1988-03-28 |
| CN1008506B (zh) | 1990-06-27 |
| CS739985A2 (en) | 1989-04-14 |
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