CS231189B2 - Herbicide agent and processing method of active matter - Google Patents
Herbicide agent and processing method of active matter Download PDFInfo
- Publication number
- CS231189B2 CS231189B2 CS819747A CS974781A CS231189B2 CS 231189 B2 CS231189 B2 CS 231189B2 CS 819747 A CS819747 A CS 819747A CS 974781 A CS974781 A CS 974781A CS 231189 B2 CS231189 B2 CS 231189B2
- Authority
- CS
- Czechoslovakia
- Prior art keywords
- bis
- methyl
- glycinate
- herbicidal composition
- active ingredient
- Prior art date
Links
- 239000004009 herbicide Substances 0.000 title description 2
- 238000003672 processing method Methods 0.000 title 1
- 239000000203 mixture Substances 0.000 claims abstract description 75
- -1 biphenylyl Chemical group 0.000 claims abstract description 68
- 230000002363 herbicidal effect Effects 0.000 claims abstract description 50
- 238000000034 method Methods 0.000 claims abstract description 35
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims abstract description 22
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims abstract description 11
- 125000001424 substituent group Chemical group 0.000 claims abstract description 9
- 125000001624 naphthyl group Chemical group 0.000 claims abstract description 7
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims abstract description 7
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 claims abstract description 6
- 229910052736 halogen Inorganic materials 0.000 claims abstract description 6
- 150000002367 halogens Chemical class 0.000 claims abstract description 6
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims abstract 6
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims abstract 4
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims description 66
- DHMQDGOQFOQNFH-UHFFFAOYSA-M Aminoacetate Chemical compound NCC([O-])=O DHMQDGOQFOQNFH-UHFFFAOYSA-M 0.000 claims description 33
- 150000001875 compounds Chemical class 0.000 claims description 28
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims description 26
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 25
- 239000004480 active ingredient Substances 0.000 claims description 17
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 17
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 claims description 10
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- 125000000217 alkyl group Chemical group 0.000 claims description 7
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 claims description 7
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- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 claims description 5
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- 239000000010 aprotic solvent Substances 0.000 claims description 5
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- 125000003545 alkoxy group Chemical group 0.000 claims description 2
- TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 claims description 2
- 229940047135 glycate Drugs 0.000 claims 2
- UAEPNZWRGJTJPN-UHFFFAOYSA-N methylcyclohexane Chemical compound CC1CCCCC1 UAEPNZWRGJTJPN-UHFFFAOYSA-N 0.000 claims 2
- 150000001721 carbon Chemical group 0.000 claims 1
- RMDZRTPOYPQNEM-UHFFFAOYSA-N methyl 2-[diphenoxyphosphorylmethyl-(4-methylphenyl)sulfanylamino]acetate Chemical group C=1C=C(C)C=CC=1SN(CC(=O)OC)CP(=O)(OC=1C=CC=CC=1)OC1=CC=CC=C1 RMDZRTPOYPQNEM-UHFFFAOYSA-N 0.000 claims 1
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- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 239000000543 intermediate Substances 0.000 description 1
- 125000006303 iodophenyl group Chemical group 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
- 229910052622 kaolinite Inorganic materials 0.000 description 1
- 239000012669 liquid formulation Substances 0.000 description 1
- 240000004308 marijuana Species 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 235000010981 methylcellulose Nutrition 0.000 description 1
- 235000019713 millet Nutrition 0.000 description 1
- 239000003595 mist Substances 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 239000012452 mother liquor Substances 0.000 description 1
- 125000006501 nitrophenyl group Chemical group 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 229910052625 palygorskite Inorganic materials 0.000 description 1
- 239000008188 pellet Substances 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 230000008654 plant damage Effects 0.000 description 1
- 238000000711 polarimetry Methods 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 239000000244 polyoxyethylene sorbitan monooleate Substances 0.000 description 1
- 235000010482 polyoxyethylene sorbitan monooleate Nutrition 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 229920000053 polysorbate 80 Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 238000011027 product recovery Methods 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 235000009566 rice Nutrition 0.000 description 1
- 239000005060 rubber Substances 0.000 description 1
- 238000005070 sampling Methods 0.000 description 1
- 229920005552 sodium lignosulfonate Polymers 0.000 description 1
- HIEHAIZHJZLEPQ-UHFFFAOYSA-M sodium;naphthalene-1-sulfonate Chemical compound [Na+].C1=CC=C2C(S(=O)(=O)[O-])=CC=CC2=C1 HIEHAIZHJZLEPQ-UHFFFAOYSA-M 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000011550 stock solution Substances 0.000 description 1
- 125000004646 sulfenyl group Chemical group S(*)* 0.000 description 1
- FWMUJAIKEJWSSY-UHFFFAOYSA-N sulfur dichloride Chemical compound ClSCl FWMUJAIKEJWSSY-UHFFFAOYSA-N 0.000 description 1
- 239000000375 suspending agent Substances 0.000 description 1
- LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound 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
- 239000012085 test solution Substances 0.000 description 1
- 238000004809 thin layer chromatography Methods 0.000 description 1
- 150000003568 thioethers Chemical class 0.000 description 1
- 150000003573 thiols Chemical class 0.000 description 1
- 125000003944 tolyl group Chemical group 0.000 description 1
- IMFACGCPASFAPR-UHFFFAOYSA-N tributylamine Chemical compound CCCCN(CCCC)CCCC IMFACGCPASFAPR-UHFFFAOYSA-N 0.000 description 1
- 239000013638 trimer Substances 0.000 description 1
- NGCRXXLKJAAUQQ-UHFFFAOYSA-N undec-5-ene Chemical compound CCCCCC=CCCCC NGCRXXLKJAAUQQ-UHFFFAOYSA-N 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 230000009105 vegetative growth Effects 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/28—Phosphorus compounds with one or more P—C bonds
- C07F9/38—Phosphonic acids [RP(=O)(OH)2]; Thiophosphonic acids ; [RP(=X1)(X2H)2(X1, X2 are each independently O, S or Se)]
- C07F9/40—Esters thereof
- C07F9/4003—Esters thereof the acid moiety containing a substituent or a structure which is considered as characteristic
- C07F9/4006—Esters of acyclic acids which can have further substituents on alkyl
-
- 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
- A01N57/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds
- A01N57/18—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-carbon bonds
- A01N57/22—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-carbon bonds containing aromatic radicals
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Dentistry (AREA)
- Engineering & Computer Science (AREA)
- Plant Pathology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Pest Control & Pesticides (AREA)
- Biochemistry (AREA)
- Molecular Biology (AREA)
- Agronomy & Crop Science (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US06/222,213 US4395374A (en) | 1981-01-02 | 1981-01-02 | Alkyl N-arylsulfenyl-N-diaryloxy-phosphinylmethylglycinates |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CS231189B2 true CS231189B2 (en) | 1984-10-15 |
Family
ID=22831337
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CS819747A CS231189B2 (en) | 1981-01-02 | 1981-12-23 | Herbicide agent and processing method of active matter |
Country Status (27)
| Country | Link |
|---|---|
| US (1) | US4395374A (ro) |
| EP (1) | EP0055925B1 (ro) |
| JP (1) | JPS57130993A (ro) |
| AR (1) | AR229038A1 (ro) |
| AT (1) | ATE11542T1 (ro) |
| AU (1) | AU542431B2 (ro) |
| BG (2) | BG38483A3 (ro) |
| BR (1) | BR8108377A (ro) |
| CA (1) | CA1185251A (ro) |
| CS (1) | CS231189B2 (ro) |
| DD (2) | DD210056A5 (ro) |
| DE (1) | DE3168706D1 (ro) |
| ES (1) | ES508294A0 (ro) |
| GB (1) | GB2090596B (ro) |
| GR (1) | GR77552B (ro) |
| HU (1) | HU186459B (ro) |
| IL (1) | IL64639A (ro) |
| IN (1) | IN156120B (ro) |
| KE (1) | KE3498A (ro) |
| NZ (1) | NZ199385A (ro) |
| PH (1) | PH18166A (ro) |
| PL (1) | PL128205B1 (ro) |
| PT (1) | PT74202B (ro) |
| RO (3) | RO84200B (ro) |
| TR (1) | TR21225A (ro) |
| ZA (1) | ZA818906B (ro) |
| ZW (1) | ZW30781A1 (ro) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| ES8603901A1 (es) * | 1983-07-27 | 1986-01-01 | Rhone Poulenc Agrochimie | Procedimiento de preparacion de sulfonamidas con grupo ansinometilfosfonico |
| EP0141794A1 (en) * | 1983-08-04 | 1985-05-15 | Monsanto Company | Aralower alkyl and substituted aralower alkyl esters of N-phosphonomethylglycines |
| US5468718A (en) * | 1985-10-21 | 1995-11-21 | Ici Americas Inc. | Liquid, phytoactive compositions and method for their preparation |
| US5202111A (en) * | 1991-05-09 | 1993-04-13 | Chesebrough-Pond's Usa Co., Division Of Conopco, Inc. | Phosphorylated polyhydroxy compounds for tartar control |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3910969A (en) * | 1974-06-28 | 1975-10-07 | Monsanto Co | N-phenylsulfonamido-n-phosphonomethyl glycine and certain derivatives thereof |
| US3991095A (en) * | 1975-12-29 | 1976-11-09 | Monsanto Company | N-thiolcarbonyl derivatives of N-phosphonomethylglycine |
| MX3898E (es) * | 1975-12-29 | 1981-09-10 | Monsanto Co | Procedimiento mejorado para la preparacion de triesteres de n-fosfonometilglicina |
| US4067719A (en) * | 1976-12-13 | 1978-01-10 | Monsanto Company | O-Aryl N-phosphonomethylglycinonitriles and the herbicidal use thereof |
| US4084953A (en) * | 1977-03-09 | 1978-04-18 | Monsanto Company | N-hydroxy-N-phosphonomethylglycines and the herbicidal use thereof |
| US4252554A (en) * | 1979-08-08 | 1981-02-24 | Monsanto Company | Herbicidal ester derivatives of N-arylthio-N-phosphonomethylglycinonitrile |
-
1981
- 1981-01-02 US US06/222,213 patent/US4395374A/en not_active Expired - Fee Related
- 1981-12-07 PL PL1981234413A patent/PL128205B1/pl unknown
- 1981-12-23 IN IN445/CAL/81A patent/IN156120B/en unknown
- 1981-12-23 NZ NZ199385A patent/NZ199385A/en unknown
- 1981-12-23 BR BR8108377A patent/BR8108377A/pt unknown
- 1981-12-23 GR GR66898A patent/GR77552B/el unknown
- 1981-12-23 CS CS819747A patent/CS231189B2/cs unknown
- 1981-12-23 CA CA000393113A patent/CA1185251A/en not_active Expired
- 1981-12-23 DE DE8181306120T patent/DE3168706D1/de not_active Expired
- 1981-12-23 RO RO106085A patent/RO84200B/ro unknown
- 1981-12-23 RO RO81114961A patent/RO88789A/ro unknown
- 1981-12-23 PH PH26671A patent/PH18166A/en unknown
- 1981-12-23 ZA ZA818906A patent/ZA818906B/xx unknown
- 1981-12-23 ZW ZW307/81A patent/ZW30781A1/xx unknown
- 1981-12-23 PT PT74202A patent/PT74202B/pt unknown
- 1981-12-23 AR AR287929A patent/AR229038A1/es active
- 1981-12-23 TR TR21225A patent/TR21225A/xx unknown
- 1981-12-23 BG BG8154660A patent/BG38483A3/xx unknown
- 1981-12-23 AU AU78812/81A patent/AU542431B2/en not_active Ceased
- 1981-12-23 DD DD81252200A patent/DD210056A5/de unknown
- 1981-12-23 HU HU813941A patent/HU186459B/hu unknown
- 1981-12-23 BG BG8360646A patent/BG38640A3/xx unknown
- 1981-12-23 DD DD81236167A patent/DD208068A5/de unknown
- 1981-12-23 RO RO81114960A patent/RO88788A/ro unknown
- 1981-12-23 JP JP56207255A patent/JPS57130993A/ja active Pending
- 1981-12-23 AT AT81306120T patent/ATE11542T1/de not_active IP Right Cessation
- 1981-12-23 GB GB8138826A patent/GB2090596B/en not_active Expired
- 1981-12-23 ES ES508294A patent/ES508294A0/es active Granted
- 1981-12-23 EP EP81306120A patent/EP0055925B1/en not_active Expired
- 1981-12-25 IL IL64639A patent/IL64639A/xx unknown
-
1985
- 1985-01-08 KE KE3498A patent/KE3498A/xx unknown
Also Published As
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