DD144712A5 - Herbizide zusammensetzung und herbizides verfahren - Google Patents
Herbizide zusammensetzung und herbizides verfahren Download PDFInfo
- Publication number
- DD144712A5 DD144712A5 DD79214211A DD21421179A DD144712A5 DD 144712 A5 DD144712 A5 DD 144712A5 DD 79214211 A DD79214211 A DD 79214211A DD 21421179 A DD21421179 A DD 21421179A DD 144712 A5 DD144712 A5 DD 144712A5
- Authority
- DD
- German Democratic Republic
- Prior art keywords
- trifluoroacetyl
- glycinate
- phenylthio
- phenoxy
- ethyl
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 40
- 230000002363 herbicidal effect Effects 0.000 title claims abstract description 28
- 238000000034 method Methods 0.000 title claims description 9
- -1 methoxy (N-piperidinoamino) phosphonomethyl Chemical group 0.000 claims abstract description 53
- DHMQDGOQFOQNFH-UHFFFAOYSA-M Aminoacetate Chemical compound NCC([O-])=O DHMQDGOQFOQNFH-UHFFFAOYSA-M 0.000 claims abstract description 22
- CICQESUWPFXOCH-UHFFFAOYSA-N [[(2-ethoxy-2-oxoethyl)-(2,2,2-trifluoroacetyl)amino]-phenylsulfanylmethyl]-(propan-2-ylamino)oxyphosphinic acid Chemical compound CCOC(=O)CN(C(=O)C(F)(F)F)C(P(O)(=O)ONC(C)C)SC1=CC=CC=C1 CICQESUWPFXOCH-UHFFFAOYSA-N 0.000 claims abstract 2
- 150000001875 compounds Chemical class 0.000 claims description 23
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 17
- 125000000217 alkyl group Chemical group 0.000 claims description 13
- 125000004414 alkyl thio group Chemical group 0.000 claims description 11
- 125000003545 alkoxy group Chemical group 0.000 claims description 6
- 125000003282 alkyl amino group Chemical group 0.000 claims description 6
- 125000004663 dialkyl amino group Chemical group 0.000 claims description 6
- 239000000654 additive Substances 0.000 claims description 5
- 125000004432 carbon atom Chemical group C* 0.000 claims description 5
- 125000004573 morpholin-4-yl group Chemical group N1(CCOCC1)* 0.000 claims description 5
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims description 5
- 230000000996 additive effect Effects 0.000 claims description 4
- 125000003356 phenylsulfanyl group Chemical group [*]SC1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 claims description 4
- 125000006319 alkynyl amino group Chemical group 0.000 claims description 3
- 125000006323 alkenyl amino group Chemical group 0.000 claims 1
- 239000001963 growth medium Substances 0.000 claims 1
- 150000002780 morpholines Chemical class 0.000 claims 1
- 239000004009 herbicide Substances 0.000 abstract description 8
- 229910052698 phosphorus Inorganic materials 0.000 abstract description 3
- QOUJAFROMRVABV-UHFFFAOYSA-N [[(2-ethoxy-2-oxoethyl)-(2,2,2-trifluoroacetyl)amino]-phenoxymethyl]-(piperidin-1-ylamino)oxyphosphinic acid Chemical compound C1CCCCN1NOP(O)(=O)C(N(CC(=O)OCC)C(=O)C(F)(F)F)OC1=CC=CC=C1 QOUJAFROMRVABV-UHFFFAOYSA-N 0.000 abstract description 2
- 125000004437 phosphorous atom Chemical group 0.000 abstract description 2
- ZHOZZXOWVJVOHF-UHFFFAOYSA-N [[(2-ethoxy-2-oxoethyl)-(2,2,2-trifluoroacetyl)amino]-phenoxymethyl]-phenylsulfanyloxyphosphinic acid Chemical compound C=1C=CC=CC=1SOP(O)(=O)C(N(CC(=O)OCC)C(=O)C(F)(F)F)OC1=CC=CC=C1 ZHOZZXOWVJVOHF-UHFFFAOYSA-N 0.000 abstract 1
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- 239000004480 active ingredient Substances 0.000 description 6
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- JMGZBMRVDHKMKB-UHFFFAOYSA-L disodium;2-sulfobutanedioate Chemical compound [Na+].[Na+].OS(=O)(=O)C(C([O-])=O)CC([O-])=O JMGZBMRVDHKMKB-UHFFFAOYSA-L 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 125000004185 ester group Chemical group 0.000 description 1
- OAYLNYINCPYISS-UHFFFAOYSA-N ethyl acetate;hexane Chemical compound CCCCCC.CCOC(C)=O OAYLNYINCPYISS-UHFFFAOYSA-N 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 150000002191 fatty alcohols Chemical class 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 125000005843 halogen group Chemical group 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 239000011487 hemp Substances 0.000 description 1
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 239000003906 humectant Substances 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 229920005610 lignin Polymers 0.000 description 1
- 238000004949 mass spectrometry Methods 0.000 description 1
- 239000002609 medium Substances 0.000 description 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 235000019713 millet Nutrition 0.000 description 1
- 238000003541 multi-stage reaction Methods 0.000 description 1
- DIAIBWNEUYXDNL-UHFFFAOYSA-N n,n-dihexylhexan-1-amine Chemical compound CCCCCCN(CCCCCC)CCCCCC DIAIBWNEUYXDNL-UHFFFAOYSA-N 0.000 description 1
- 239000006199 nebulizer Substances 0.000 description 1
- SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical compound CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 1
- 230000000269 nucleophilic effect Effects 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 239000008188 pellet Substances 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 125000002743 phosphorus functional group Chemical group 0.000 description 1
- 230000008635 plant growth Effects 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 150000003254 radicals Chemical class 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 235000009566 rice Nutrition 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000000377 silicon dioxide Substances 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
- 239000008247 solid mixture Substances 0.000 description 1
- 239000011550 stock solution Substances 0.000 description 1
- 230000036561 sun exposure Effects 0.000 description 1
- 239000000375 suspending agent Substances 0.000 description 1
- 239000003784 tall oil Substances 0.000 description 1
- IMFACGCPASFAPR-UHFFFAOYSA-N tributylamine Chemical compound CCCCN(CCCC)CCCC IMFACGCPASFAPR-UHFFFAOYSA-N 0.000 description 1
- 150000005691 triesters Chemical class 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
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
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/6527—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having nitrogen and oxygen atoms as the only ring hetero atoms
- C07F9/6533—Six-membered rings
-
- 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
-
- 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
- A01N57/26—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-nitrogen bonds
-
- 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
-
- 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)]
- C07F9/44—Amides thereof
- C07F9/4403—Amides thereof the acid moiety containing a substituent or a structure which is considered as characteristic
- C07F9/4407—Amides of acyclic saturated acids which can have further substituents on alkyl
-
- 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
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/553—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having one nitrogen atom as the only ring hetero atom
- C07F9/576—Six-membered rings
- C07F9/59—Hydrogenated pyridine rings
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Organic Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Health & Medical Sciences (AREA)
- Biochemistry (AREA)
- Molecular Biology (AREA)
- Dentistry (AREA)
- Engineering & Computer Science (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Plant Pathology (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US05/922,930 US4180394A (en) | 1978-07-10 | 1978-07-10 | Derivatives of N-trifluoroacetyl-N-phosphonomethylglycinates and the herbicidal use thereof |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DD144712A5 true DD144712A5 (de) | 1980-11-05 |
Family
ID=25447814
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DD79214211A DD144712A5 (de) | 1978-07-10 | 1979-07-09 | Herbizide zusammensetzung und herbizides verfahren |
Country Status (19)
| Country | Link |
|---|---|
| US (1) | US4180394A (es) |
| EP (1) | EP0007211B1 (es) |
| JP (1) | JPS5513293A (es) |
| AR (1) | AR230749A1 (es) |
| AU (1) | AU520850B2 (es) |
| BG (1) | BG30625A3 (es) |
| BR (1) | BR7904352A (es) |
| CA (1) | CA1121819A (es) |
| CS (1) | CS209928B2 (es) |
| DD (1) | DD144712A5 (es) |
| DE (1) | DE2966181D1 (es) |
| DK (1) | DK147915C (es) |
| HU (1) | HU185006B (es) |
| IL (1) | IL57749A (es) |
| MX (1) | MX5594E (es) |
| PH (1) | PH15633A (es) |
| PL (1) | PL116631B1 (es) |
| RO (2) | RO89361A (es) |
| ZA (1) | ZA793413B (es) |
Families Citing this family (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4353731A (en) * | 1978-07-10 | 1982-10-12 | Monsanto Company | Amide and hydrazide derivatives of N-trifluoroacetyl-N-phosphonomethylglycine |
| US4421549A (en) * | 1979-12-26 | 1983-12-20 | Monsanto Company | Amido and hydrazido derivatives of N-trifluoroacetyl-N-phosphinothioylmethylglycine esters |
| DE3264720D1 (en) * | 1981-03-11 | 1985-08-22 | Monsanto Co | N-formyl-n-phosphonomethylglycine and esters thereof as herbicides |
| US4444580A (en) * | 1982-11-01 | 1984-04-24 | Monsanto Company | N-Substituted N-(phosphonomethyl)aminoethanal derivatives as herbicides |
| US4569802A (en) * | 1983-06-27 | 1986-02-11 | Stauffer Chemical Company | Method for preparation of N-phosphonomethylglycine |
| US4545804A (en) * | 1983-11-21 | 1985-10-08 | Monsanto Company | N(Aminophosphinylmethyl) glycine derivatives |
| US5580841A (en) * | 1985-05-29 | 1996-12-03 | Zeneca Limited | Solid, phytoactive compositions and method for their preparation |
| US5468718A (en) * | 1985-10-21 | 1995-11-21 | Ici Americas Inc. | Liquid, phytoactive compositions and method for their preparation |
| US8470741B2 (en) * | 2003-05-07 | 2013-06-25 | Croda Americas Llc | Homogeneous liquid saccharide and oil systems |
Family Cites Families (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3799758A (en) * | 1971-08-09 | 1974-03-26 | Monsanto Co | N-phosphonomethyl-glycine phytotoxicant compositions |
| PH16509A (en) * | 1971-03-10 | 1983-11-08 | Monsanto Co | N-phosphonomethylglycine phytotoxicant composition |
| US3853530A (en) * | 1971-03-10 | 1974-12-10 | Monsanto Co | Regulating plants with n-phosphonomethylglycine and derivatives thereof |
| RO67869A (ro) * | 1972-12-11 | 1981-06-22 | Mensanto Co,Us | Procedeu pentru prepararea unor derivati ai n-fosfonometil-gliciu n-oxizilor |
| US3835000A (en) * | 1972-12-21 | 1974-09-10 | Monsanto Co | Electrolytic process for producing n-phosphonomethyl glycine |
| US3933946A (en) * | 1974-11-19 | 1976-01-20 | Monsanto Company | N-hydroxy-N-phosphonomethylglycinates |
| US4047926A (en) * | 1975-05-23 | 1977-09-13 | Monsanto Company | Treatment of sugarcane with N-(perfluoroacyl)-N-phosphonomethyl glycine |
| US3970695A (en) * | 1975-05-23 | 1976-07-20 | Monsanto Company | N-(perfluoroacyl)-N-phosphonomethyl glycine compounds, method of preparing same |
| MX3898E (es) | 1975-12-29 | 1981-09-10 | Monsanto Co | Procedimiento mejorado para la preparacion de triesteres de n-fosfonometilglicina |
| US4053505A (en) * | 1976-01-05 | 1977-10-11 | Monsanto Company | Preparation of n-phosphonomethyl glycine |
-
1978
- 1978-07-10 US US05/922,930 patent/US4180394A/en not_active Expired - Lifetime
-
1979
- 1979-07-06 DE DE7979301308T patent/DE2966181D1/de not_active Expired
- 1979-07-06 EP EP79301308A patent/EP0007211B1/en not_active Expired
- 1979-07-06 AR AR277213A patent/AR230749A1/es active
- 1979-07-09 CS CS794815A patent/CS209928B2/cs unknown
- 1979-07-09 BR BR7904352A patent/BR7904352A/pt unknown
- 1979-07-09 RO RO79115573A patent/RO89361A/ro unknown
- 1979-07-09 HU HU79MO1053A patent/HU185006B/hu unknown
- 1979-07-09 BG BG044254A patent/BG30625A3/xx unknown
- 1979-07-09 AU AU48775/79A patent/AU520850B2/en not_active Ceased
- 1979-07-09 DD DD79214211A patent/DD144712A5/de unknown
- 1979-07-09 RO RO98095A patent/RO78765B/ro unknown
- 1979-07-09 PH PH22752A patent/PH15633A/en unknown
- 1979-07-09 MX MX798168U patent/MX5594E/es unknown
- 1979-07-09 JP JP8737979A patent/JPS5513293A/ja active Pending
- 1979-07-09 IL IL57749A patent/IL57749A/xx unknown
- 1979-07-09 PL PL1979216975A patent/PL116631B1/pl unknown
- 1979-07-09 ZA ZA793413A patent/ZA793413B/xx unknown
- 1979-07-09 CA CA000331415A patent/CA1121819A/en not_active Expired
- 1979-07-09 DK DK287779A patent/DK147915C/da not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| RO78765A (ro) | 1984-10-30 |
| RO89361A (ro) | 1986-05-30 |
| DE2966181D1 (en) | 1983-10-27 |
| IL57749A (en) | 1983-12-30 |
| CA1121819A (en) | 1982-04-13 |
| AR230749A1 (es) | 1984-06-29 |
| BR7904352A (pt) | 1980-04-08 |
| PH15633A (en) | 1983-03-11 |
| JPS5513293A (en) | 1980-01-30 |
| ZA793413B (en) | 1980-07-30 |
| EP0007211A1 (en) | 1980-01-23 |
| DK147915C (da) | 1985-06-17 |
| CS209928B2 (en) | 1981-12-31 |
| AU4877579A (en) | 1980-02-07 |
| PL116631B1 (en) | 1981-06-30 |
| RO78765B (ro) | 1984-11-30 |
| PL216975A1 (es) | 1980-05-05 |
| EP0007211B1 (en) | 1983-09-21 |
| HU185006B (en) | 1984-11-28 |
| BG30625A3 (en) | 1981-07-15 |
| IL57749A0 (en) | 1979-11-30 |
| AU520850B2 (en) | 1982-03-04 |
| DK147915B (da) | 1985-01-07 |
| DK287779A (da) | 1980-01-11 |
| MX5594E (es) | 1983-11-03 |
| US4180394A (en) | 1979-12-25 |
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