CS232728B2 - Herbicide agent - Google Patents
Herbicide agent Download PDFInfo
- Publication number
- CS232728B2 CS232728B2 CS825202A CS520282A CS232728B2 CS 232728 B2 CS232728 B2 CS 232728B2 CS 825202 A CS825202 A CS 825202A CS 520282 A CS520282 A CS 520282A CS 232728 B2 CS232728 B2 CS 232728B2
- Authority
- CS
- Czechoslovakia
- Prior art keywords
- ethyl
- acid
- radical
- weight
- propyl
- Prior art date
Links
- 239000004009 herbicide Substances 0.000 title abstract description 6
- 239000000203 mixture Substances 0.000 claims abstract description 32
- 230000002363 herbicidal effect Effects 0.000 claims abstract description 24
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims abstract description 13
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 claims abstract description 10
- 150000001875 compounds Chemical class 0.000 claims abstract description 7
- -1 hexamethylene radical Chemical class 0.000 claims abstract description 7
- OCBFFGCSTGGPSQ-UHFFFAOYSA-N [CH2]CC Chemical group [CH2]CC OCBFFGCSTGGPSQ-UHFFFAOYSA-N 0.000 claims abstract description 6
- 239000000654 additive Substances 0.000 claims abstract description 6
- 229930195733 hydrocarbon Natural products 0.000 claims abstract description 5
- 150000002430 hydrocarbons Chemical class 0.000 claims abstract description 5
- 239000007788 liquid Substances 0.000 claims abstract description 5
- KTOQRRDVVIDEAA-UHFFFAOYSA-N 2-methylpropane Chemical compound [CH2]C(C)C KTOQRRDVVIDEAA-UHFFFAOYSA-N 0.000 claims abstract description 4
- 239000004215 Carbon black (E152) Substances 0.000 claims abstract description 4
- YUDRVAHLXDBKSR-UHFFFAOYSA-N [CH]1CCCCC1 Chemical compound [CH]1CCCCC1 YUDRVAHLXDBKSR-UHFFFAOYSA-N 0.000 claims abstract description 4
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 claims abstract description 4
- 238000009835 boiling Methods 0.000 claims abstract description 3
- QUPDWYMUPZLYJZ-UHFFFAOYSA-N ethyl Chemical group C[CH2] QUPDWYMUPZLYJZ-UHFFFAOYSA-N 0.000 claims abstract description 3
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims abstract description 3
- BMTAFVWTTFSTOG-UHFFFAOYSA-N Butylate Chemical compound CCSC(=O)N(CC(C)C)CC(C)C BMTAFVWTTFSTOG-UHFFFAOYSA-N 0.000 claims description 13
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 8
- 239000003350 kerosene Substances 0.000 claims description 8
- 239000013543 active substance Substances 0.000 claims description 6
- 239000003208 petroleum Substances 0.000 claims description 6
- 239000002253 acid Substances 0.000 claims description 5
- WBIQQQGBSDOWNP-UHFFFAOYSA-N 2-dodecylbenzenesulfonic acid Chemical compound CCCCCCCCCCCCC1=CC=CC=C1S(O)(=O)=O WBIQQQGBSDOWNP-UHFFFAOYSA-N 0.000 claims description 4
- 229940060296 dodecylbenzenesulfonic acid Drugs 0.000 claims description 4
- 229920000151 polyglycol Polymers 0.000 claims description 4
- 239000010695 polyglycol Substances 0.000 claims description 4
- SGEJQUSYQTVSIU-UHFFFAOYSA-N Pebulate Chemical compound CCCCN(CC)C(=O)SCCC SGEJQUSYQTVSIU-UHFFFAOYSA-N 0.000 claims description 2
- 150000002191 fatty alcohols Chemical class 0.000 claims description 2
- GUVLYNGULCJVDO-UHFFFAOYSA-N EPTC Chemical compound CCCN(CCC)C(=O)SCC GUVLYNGULCJVDO-UHFFFAOYSA-N 0.000 claims 6
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 1
- 241000196324 Embryophyta Species 0.000 abstract description 24
- 230000000996 additive effect Effects 0.000 abstract description 2
- 239000003905 agrochemical Substances 0.000 abstract 1
- 238000009472 formulation Methods 0.000 abstract 1
- 229910002091 carbon monoxide Inorganic materials 0.000 description 13
- 239000000126 substance Substances 0.000 description 12
- 239000004495 emulsifiable concentrate Substances 0.000 description 10
- 239000002689 soil Substances 0.000 description 10
- 238000002474 experimental method Methods 0.000 description 9
- QWWHRELOCZEQNZ-UHFFFAOYSA-N 2,2-dichloro-1-(1-oxa-4-azaspiro[4.5]decan-4-yl)ethanone Chemical compound ClC(Cl)C(=O)N1CCOC11CCCCC1 QWWHRELOCZEQNZ-UHFFFAOYSA-N 0.000 description 7
- OKUGPJPKMAEJOE-UHFFFAOYSA-N S-propyl dipropylcarbamothioate Chemical compound CCCSC(=O)N(CCC)CCC OKUGPJPKMAEJOE-UHFFFAOYSA-N 0.000 description 7
- 239000004480 active ingredient Substances 0.000 description 7
- 238000011282 treatment Methods 0.000 description 7
- 230000000694 effects Effects 0.000 description 6
- 230000002195 synergetic effect Effects 0.000 description 6
- 150000003558 thiocarbamic acid derivatives Chemical class 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- 239000003795 chemical substances by application Substances 0.000 description 5
- 238000011156 evaluation Methods 0.000 description 5
- 238000000034 method Methods 0.000 description 5
- 238000012360 testing method Methods 0.000 description 5
- DFCAFRGABIXSDS-UHFFFAOYSA-N Cycloate Chemical compound CCSC(=O)N(CC)C1CCCCC1 DFCAFRGABIXSDS-UHFFFAOYSA-N 0.000 description 3
- 241000209510 Liliopsida Species 0.000 description 3
- NCPDPTXSMJDCIH-UHFFFAOYSA-N dipropylcarbamothioic s-acid Chemical compound CCCN(C(S)=O)CCC NCPDPTXSMJDCIH-UHFFFAOYSA-N 0.000 description 3
- 239000004094 surface-active agent Substances 0.000 description 3
- 235000006463 Brassica alba Nutrition 0.000 description 2
- 244000140786 Brassica hirta Species 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- 125000001931 aliphatic group Chemical group 0.000 description 2
- 239000000729 antidote Substances 0.000 description 2
- 239000012141 concentrate Substances 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- DEDOPGXGGQYYMW-UHFFFAOYSA-N molinate Chemical compound CCSC(=O)N1CCCCCC1 DEDOPGXGGQYYMW-UHFFFAOYSA-N 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 241000209761 Avena Species 0.000 description 1
- 235000007320 Avena fatua Nutrition 0.000 description 1
- 241000209764 Avena fatua Species 0.000 description 1
- 235000007319 Avena orientalis Nutrition 0.000 description 1
- 235000011371 Brassica hirta Nutrition 0.000 description 1
- 241001110521 Cyperus fuscus Species 0.000 description 1
- 206010011878 Deafness Diseases 0.000 description 1
- 240000006240 Linum usitatissimum Species 0.000 description 1
- 235000004431 Linum usitatissimum Nutrition 0.000 description 1
- IGFHQQFPSIBGKE-UHFFFAOYSA-N Nonylphenol Natural products CCCCCCCCCC1=CC=C(O)C=C1 IGFHQQFPSIBGKE-UHFFFAOYSA-N 0.000 description 1
- JWOLLWQJKQOEOL-UHFFFAOYSA-N OOOOOOOOOOOOO Chemical compound OOOOOOOOOOOOO JWOLLWQJKQOEOL-UHFFFAOYSA-N 0.000 description 1
- 241000972349 Ocoa Species 0.000 description 1
- 231100000674 Phytotoxicity Toxicity 0.000 description 1
- 230000002730 additional effect Effects 0.000 description 1
- 229940075522 antidotes Drugs 0.000 description 1
- 229910052793 cadmium Inorganic materials 0.000 description 1
- GNVMUORYQLCPJZ-UHFFFAOYSA-N carbamothioic s-acid Chemical compound NC(S)=O GNVMUORYQLCPJZ-UHFFFAOYSA-N 0.000 description 1
- 125000004836 hexamethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[*:1] 0.000 description 1
- SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical compound CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 1
- 230000000885 phytotoxic effect Effects 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 229910052703 rhodium Inorganic materials 0.000 description 1
- 230000001502 supplementing effect Effects 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
-
- 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
- A01N47/16—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof the nitrogen atom being part 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)
- Catching Or Destruction (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| HU811975A HU184467B (en) | 1981-07-08 | 1981-07-08 | Herbicide composition containing the mixture of two active agents |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CS520282A2 CS520282A2 (en) | 1984-02-13 |
| CS232728B2 true CS232728B2 (en) | 1985-02-14 |
Family
ID=10957104
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CS825202A CS232728B2 (en) | 1981-07-08 | 1982-07-07 | Herbicide agent |
Country Status (18)
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3585651D1 (de) * | 1984-09-19 | 1992-04-23 | Stauffer Chemical Co | Herbizide zusammensetzungen mit laengerer lebensdauer im boden. |
| USD926637S1 (en) * | 2018-08-23 | 2021-08-03 | Pexco Gmbh | Cycle or motorcycle frame component |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NL213753A (enrdf_load_stackoverflow) * | 1956-01-17 | |||
| US3175897A (en) * | 1962-08-21 | 1965-03-30 | Stauffer Chemical Co | Asymmetric thiolcarbamates as herbicides |
| JPS52128221A (en) * | 1976-04-20 | 1977-10-27 | Mitsubishi Petrochem Co Ltd | Herbicidal accelerators |
| DE2909158A1 (de) * | 1979-03-08 | 1980-09-11 | Basf Ag | Herbizide mischungen |
-
1981
- 1981-07-08 HU HU811975A patent/HU184467B/hu not_active IP Right Cessation
-
1982
- 1982-06-15 AT AT0231782A patent/AT381208B/de not_active IP Right Cessation
- 1982-07-02 BE BE0/208517A patent/BE893739A/fr not_active IP Right Cessation
- 1982-07-05 FR FR8211754A patent/FR2509136B1/fr not_active Expired
- 1982-07-06 PL PL1982237300A patent/PL130154B1/pl unknown
- 1982-07-07 CA CA000406774A patent/CA1182656A/en not_active Expired
- 1982-07-07 NL NL8202720A patent/NL8202720A/nl not_active Application Discontinuation
- 1982-07-07 SU SU823460409A patent/SU1494851A3/ru active
- 1982-07-07 PT PT75200A patent/PT75200B/pt unknown
- 1982-07-07 IT IT22291/82A patent/IT1156106B/it active
- 1982-07-07 DK DK305782A patent/DK305782A/da not_active Application Discontinuation
- 1982-07-07 CH CH4142/82A patent/CH653214A5/de not_active IP Right Cessation
- 1982-07-07 GB GB08219652A patent/GB2101889B/en not_active Expired
- 1982-07-07 CS CS825202A patent/CS232728B2/cs unknown
- 1982-07-07 BG BG057320A patent/BG41474A3/xx unknown
- 1982-07-07 GR GR68678A patent/GR76523B/el unknown
- 1982-07-07 IE IE1642/82A patent/IE53231B1/en unknown
- 1982-07-08 DE DE19823225624 patent/DE3225624A1/de not_active Withdrawn
Also Published As
| Publication number | Publication date |
|---|---|
| BE893739A (fr) | 1982-11-03 |
| PL130154B1 (en) | 1984-07-31 |
| GB2101889B (en) | 1985-05-01 |
| IT8222291A0 (it) | 1982-07-07 |
| IT8222291A1 (it) | 1984-01-07 |
| BG41474A3 (en) | 1987-06-15 |
| IT1156106B (it) | 1987-01-28 |
| GB2101889A (en) | 1983-01-26 |
| PL237300A1 (en) | 1983-02-14 |
| ATA231782A (de) | 1986-02-15 |
| IE53231B1 (en) | 1988-09-14 |
| PT75200B (en) | 1984-06-27 |
| DK305782A (da) | 1983-01-09 |
| PT75200A (en) | 1982-08-01 |
| AT381208B (de) | 1986-09-10 |
| GR76523B (enrdf_load_stackoverflow) | 1984-08-10 |
| CH653214A5 (de) | 1985-12-31 |
| DE3225624A1 (de) | 1983-02-03 |
| SU1494851A3 (ru) | 1989-07-15 |
| CA1182656A (en) | 1985-02-19 |
| FR2509136A1 (fr) | 1983-01-14 |
| FR2509136B1 (fr) | 1986-08-22 |
| IE821642L (en) | 1983-01-08 |
| HU184467B (en) | 1984-08-28 |
| CS520282A2 (en) | 1984-02-13 |
| NL8202720A (nl) | 1983-02-01 |
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