FI69848C - Fosfoniumsalt av n-fosfonometylglycin och deras anvaendning so herbicider och reglerare av vaexters tillvaext - Google Patents
Fosfoniumsalt av n-fosfonometylglycin och deras anvaendning so herbicider och reglerare av vaexters tillvaext Download PDFInfo
- Publication number
- FI69848C FI69848C FI822547A FI822547A FI69848C FI 69848 C FI69848 C FI 69848C FI 822547 A FI822547 A FI 822547A FI 822547 A FI822547 A FI 822547A FI 69848 C FI69848 C FI 69848C
- Authority
- FI
- Finland
- Prior art keywords
- phenyl
- alkyl
- benzyl
- phosphonomethylglycine
- independently
- Prior art date
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- NTNZTEQNFHNYBC-UHFFFAOYSA-N ethyl 2-aminoacetate Chemical compound CCOC(=O)CN NTNZTEQNFHNYBC-UHFFFAOYSA-N 0.000 description 1
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- 239000000835 fiber Substances 0.000 description 1
- 239000012065 filter cake Substances 0.000 description 1
- 238000005189 flocculation Methods 0.000 description 1
- 230000016615 flocculation Effects 0.000 description 1
- 230000000855 fungicidal effect Effects 0.000 description 1
- 239000000417 fungicide Substances 0.000 description 1
- 230000002068 genetic effect Effects 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- ZEKANFGSDXODPD-UHFFFAOYSA-N glyphosate-isopropylammonium Chemical compound CC(C)N.OC(=O)CNCP(O)(O)=O ZEKANFGSDXODPD-UHFFFAOYSA-N 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 235000021021 grapes Nutrition 0.000 description 1
- 239000005556 hormone Substances 0.000 description 1
- 229940088597 hormone Drugs 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
- JJWLVOIRVHMVIS-UHFFFAOYSA-N isopropylamine Chemical class CC(C)N JJWLVOIRVHMVIS-UHFFFAOYSA-N 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
- 150000002576 ketones Chemical class 0.000 description 1
- 239000012263 liquid product Substances 0.000 description 1
- XCOBTUNSZUJCDH-UHFFFAOYSA-B lithium magnesium sodium silicate Chemical compound [Li+].[Li+].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[Na+].[Na+].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3.O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3.O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3.O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3.O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3.O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3 XCOBTUNSZUJCDH-UHFFFAOYSA-B 0.000 description 1
- 239000000391 magnesium silicate Substances 0.000 description 1
- 235000012243 magnesium silicates Nutrition 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- STSCGYXBGNNIHH-UHFFFAOYSA-N methyl-tris(4-methylphenyl)phosphanium Chemical class C1=CC(C)=CC=C1[P+](C)(C=1C=CC(C)=CC=1)C1=CC=C(C)C=C1 STSCGYXBGNNIHH-UHFFFAOYSA-N 0.000 description 1
- SUQPXWWSBRNXEE-UHFFFAOYSA-M methyl-tris(4-methylphenyl)phosphanium;iodide Chemical compound [I-].C1=CC(C)=CC=C1[P+](C)(C=1C=CC(C)=CC=1)C1=CC=C(C)C=C1 SUQPXWWSBRNXEE-UHFFFAOYSA-M 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 239000010445 mica Substances 0.000 description 1
- 229910052618 mica group Inorganic materials 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 235000010460 mustard Nutrition 0.000 description 1
- GLENXXAWVZPRJI-UHFFFAOYSA-N n-propyldodecan-1-amine;sodium Chemical compound [Na].CCCCCCCCCCCCNCCC GLENXXAWVZPRJI-UHFFFAOYSA-N 0.000 description 1
- 231100001160 nonlethal Toxicity 0.000 description 1
- 231100001184 nonphytotoxic Toxicity 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 239000003415 peat Substances 0.000 description 1
- 239000008188 pellet Substances 0.000 description 1
- 230000035790 physiological processes and functions Effects 0.000 description 1
- 230000008654 plant damage Effects 0.000 description 1
- 229920000056 polyoxyethylene ether Polymers 0.000 description 1
- 239000000256 polyoxyethylene sorbitan monolaurate Substances 0.000 description 1
- 235000010486 polyoxyethylene sorbitan monolaurate Nutrition 0.000 description 1
- 235000012015 potatoes Nutrition 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 229910052903 pyrophyllite Inorganic materials 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 239000011435 rock Substances 0.000 description 1
- 230000021749 root development Effects 0.000 description 1
- FSYKKLYZXJSNPZ-UHFFFAOYSA-N sarcosine Chemical compound C[NH2+]CC([O-])=O FSYKKLYZXJSNPZ-UHFFFAOYSA-N 0.000 description 1
- 150000005619 secondary aliphatic amines Chemical class 0.000 description 1
- 210000002966 serum Anatomy 0.000 description 1
- 239000004460 silage Substances 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- HKZLPVFGJNLROG-UHFFFAOYSA-M silver monochloride Chemical compound [Cl-].[Ag+] HKZLPVFGJNLROG-UHFFFAOYSA-M 0.000 description 1
- 229910001961 silver nitrate Inorganic materials 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- HWCHICTXVOMIIF-UHFFFAOYSA-M sodium;3-(dodecylamino)propanoate Chemical compound [Na+].CCCCCCCCCCCCNCCC([O-])=O HWCHICTXVOMIIF-UHFFFAOYSA-M 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 238000003892 spreading Methods 0.000 description 1
- 230000007480 spreading Effects 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 235000000346 sugar Nutrition 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
- 150000003871 sulfonates Chemical class 0.000 description 1
- 125000001273 sulfonato group Chemical group [O-]S(*)(=O)=O 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 239000006228 supernatant Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 150000003510 tertiary aliphatic amines Chemical class 0.000 description 1
- 239000012085 test solution Substances 0.000 description 1
- RKHXQBLJXBGEKF-UHFFFAOYSA-M tetrabutylphosphanium;bromide Chemical compound [Br-].CCCC[P+](CCCC)(CCCC)CCCC RKHXQBLJXBGEKF-UHFFFAOYSA-M 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- TVVPMLFGPYQGTG-UHFFFAOYSA-M tetramethylphosphanium;iodide Chemical compound [I-].C[P+](C)(C)C TVVPMLFGPYQGTG-UHFFFAOYSA-M 0.000 description 1
- AEFPPQGZJFTXDR-UHFFFAOYSA-M tetraphenylphosphanium;iodide Chemical compound [I-].C1=CC=CC=C1[P+](C=1C=CC=CC=1)(C=1C=CC=CC=1)C1=CC=CC=C1 AEFPPQGZJFTXDR-UHFFFAOYSA-M 0.000 description 1
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 1
- 230000001052 transient effect Effects 0.000 description 1
- QORWJWZARLRLPR-UHFFFAOYSA-H tricalcium bis(phosphate) Chemical compound [Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O QORWJWZARLRLPR-UHFFFAOYSA-H 0.000 description 1
- ITPUYOMXIFNXBE-UHFFFAOYSA-N tris(4-chlorophenyl)-methylphosphanium Chemical class C=1C=C(Cl)C=CC=1[P+](C=1C=CC(Cl)=CC=1)(C)C1=CC=C(Cl)C=C1 ITPUYOMXIFNXBE-UHFFFAOYSA-N 0.000 description 1
- LEUMZBWALJOLOV-UHFFFAOYSA-N tris(4-methoxyphenyl)-methylphosphanium Chemical class C1=CC(OC)=CC=C1[P+](C)(C=1C=CC(OC)=CC=1)C1=CC=C(OC)C=C1 LEUMZBWALJOLOV-UHFFFAOYSA-N 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 235000013311 vegetables Nutrition 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
- C07F9/54—Quaternary phosphonium compounds
-
- 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
- A01N57/20—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-carbon bonds containing acyclic or cycloaliphatic radicals
-
- 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
- A01N57/34—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-halogen bonds; Phosphonium salts
-
- 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)]
- C07F9/3804—Phosphonic acids [RP(=O)(OH)2]; Thiophosphonic acids ; [RP(=X1)(X2H)2(X1, X2 are each independently O, S or Se)] not used, see subgroups
- C07F9/3808—Acyclic saturated acids which can have further substituents on alkyl
- C07F9/3813—N-Phosphonomethylglycine; Salts or complexes thereof
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 (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US06/295,345 US4341549A (en) | 1981-08-24 | 1981-08-24 | Phosphonium salts of N-phosphonomethylglycine and their use as herbicides and plant growth regulants |
| US29534581 | 1981-08-24 | ||
| US37453982 | 1982-05-05 | ||
| US06/374,539 US4525202A (en) | 1981-08-24 | 1982-05-05 | Phosphonium salts of N-phosphonomethylglycine and their use as herbicides and plant growth regulants |
Publications (4)
| Publication Number | Publication Date |
|---|---|
| FI822547A0 FI822547A0 (fi) | 1982-07-20 |
| FI822547L FI822547L (fi) | 1983-02-25 |
| FI69848B FI69848B (fi) | 1985-12-31 |
| FI69848C true FI69848C (fi) | 1986-05-26 |
Family
ID=26969068
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| FI822547A FI69848C (fi) | 1981-08-24 | 1982-07-20 | Fosfoniumsalt av n-fosfonometylglycin och deras anvaendning so herbicider och reglerare av vaexters tillvaext |
Country Status (13)
| Country | Link |
|---|---|
| US (1) | US4525202A (da) |
| EP (1) | EP0073574B1 (da) |
| CS (1) | CS227697B2 (da) |
| DE (1) | DE3267430D1 (da) |
| DK (1) | DK313582A (da) |
| FI (1) | FI69848C (da) |
| GR (1) | GR77267B (da) |
| IL (1) | IL66226A0 (da) |
| NO (1) | NO822526L (da) |
| NZ (1) | NZ201356A (da) |
| PH (1) | PH18343A (da) |
| PT (1) | PT75241B (da) |
| TR (1) | TR21496A (da) |
Families Citing this family (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GR81556B (da) * | 1983-05-09 | 1984-12-11 | Stauffer Chemical Co | |
| ES8603901A1 (es) * | 1983-07-27 | 1986-01-01 | Rhone Poulenc Agrochimie | Procedimiento de preparacion de sulfonamidas con grupo ansinometilfosfonico |
| DE3442690A1 (de) * | 1984-11-23 | 1986-05-28 | Hoechst Ag, 6230 Frankfurt | Salze von 1-phenyl-imidazol-5-carbonsaeuren, ein verfahren zu ihrer herstellung und ihre verwendung als wachstumsregulatoren |
| EP0453580A1 (en) * | 1990-03-01 | 1991-10-30 | Shell Internationale Researchmaatschappij B.V. | Fungicidal benzyl-tris(aryl)-phosphonium salts |
| US6930075B1 (en) | 1990-11-02 | 2005-08-16 | Monsanto Technology, Llc | Fatty acid-based herbicidal composition |
| IL101539A (en) * | 1991-04-16 | 1998-09-24 | Monsanto Europe Sa | Mono-ammonium salts of the history of N phosphonomethyl glycyl which are not hygroscopes, their preparations and pesticides containing |
| CA2075003C (en) * | 1991-08-02 | 1999-01-19 | James Web Kassebaum | Herbicidal compositions and methods of preparing and using the same |
| US8192633B2 (en) * | 1998-07-06 | 2012-06-05 | Grott Gerald J | Methods of energy storage and transfer |
| US7717173B2 (en) * | 1998-07-06 | 2010-05-18 | Ecycling, LLC | Methods of improving oil or gas production with recycled, increased sodium water |
| AUPR682201A0 (en) | 2001-08-03 | 2001-08-30 | Nufarm Limited | Glyphosate composition |
| US8268749B2 (en) * | 2004-09-17 | 2012-09-18 | Monsanto Technology Llc | Fast symptom glyphosate formulations |
| US20070023359A1 (en) * | 2005-07-29 | 2007-02-01 | Grott Gerald J | Methods of the purification and use of moderately saline water particularly for use in aquaculture, horticulture and, agriculture |
| DE102005059467A1 (de) * | 2005-12-13 | 2007-06-14 | Bayer Cropscience Ag | Insektizide Zusammensetzungen mit verbesserter Wirkung |
| DE102005059466A1 (de) * | 2005-12-13 | 2007-06-14 | Bayer Cropscience Ag | Insektizide Zusammensetzungen mit verbesserter Wirkung |
| US20100051556A1 (en) * | 2008-08-29 | 2010-03-04 | Grott Gerald J | Methods of purifiying water using waste brines to regenerate ion-exchange resins |
| PL2341778T3 (pl) | 2008-11-06 | 2014-06-30 | Sn Biotech Tech Sp Z O O Sp K | Ciekła, homogeniczna kompozycja herbicydowa, sposób zwalczania chwastów, sposób wytwarzania ciekłej, homogenicznej kompozycji herbicydu i zastosowanie ciekłej, homogenicznej kompozycji herbicydowej do zwalczania chwastów |
| US20100147767A1 (en) * | 2008-12-15 | 2010-06-17 | Grott Gerald J | Method for purifying waste saline waters without reagent waste |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3230069A (en) * | 1958-08-27 | 1966-01-18 | Plant Introduction Station | Method of inhibiting plant growth |
| US3364107A (en) * | 1965-08-23 | 1968-01-16 | American Cyanamid Co | Controlling algae, bacteria, and fungi growth with alpha, omega-alkylenebis[triphenyl-phosphonium salt] |
| US3556762A (en) * | 1968-10-21 | 1971-01-19 | Monsanto Co | Increasing carbohydrate deposition in plants with aminophosphonates |
| US3847947A (en) * | 1970-03-11 | 1974-11-12 | Chemagro Corp | Quaternary thenyl phosphonium salts |
| US3799758A (en) * | 1971-08-09 | 1974-03-26 | Monsanto Co | N-phosphonomethyl-glycine phytotoxicant compositions |
| US3977860A (en) * | 1971-08-09 | 1976-08-31 | Monsanto Company | Herbicidal compositions and methods employing esters of N-phosphonomethylglycine |
| US3929450A (en) * | 1974-06-28 | 1975-12-30 | Monsanto Co | Herbicidal compositions and methods |
| DE2860342D1 (en) * | 1977-08-11 | 1981-02-12 | Ciba Geigy Ag | Glycylmethyl-phosphinic acid derivatives, their preparation and their use |
| US4315765A (en) * | 1980-12-04 | 1982-02-16 | Stauffer Chemical Company | Trialkylsulfonium salts of n-phosphonomethylglycine and their use as plant growth regulators and herbicides |
-
1982
- 1982-05-05 US US06/374,539 patent/US4525202A/en not_active Expired - Fee Related
- 1982-07-05 IL IL66226A patent/IL66226A0/xx unknown
- 1982-07-13 DK DK313582A patent/DK313582A/da not_active Application Discontinuation
- 1982-07-13 GR GR68743A patent/GR77267B/el unknown
- 1982-07-14 PT PT75241A patent/PT75241B/pt unknown
- 1982-07-15 CS CS825440A patent/CS227697B2/cs unknown
- 1982-07-16 TR TR21496A patent/TR21496A/xx unknown
- 1982-07-20 FI FI822547A patent/FI69848C/fi not_active IP Right Cessation
- 1982-07-22 NZ NZ201356A patent/NZ201356A/en unknown
- 1982-07-22 NO NO822526A patent/NO822526L/no unknown
- 1982-07-23 PH PH27625A patent/PH18343A/en unknown
- 1982-08-02 EP EP82304068A patent/EP0073574B1/en not_active Expired
- 1982-08-02 DE DE8282304068T patent/DE3267430D1/de not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| EP0073574B1 (en) | 1985-11-13 |
| NZ201356A (en) | 1984-10-19 |
| DE3267430D1 (en) | 1985-12-19 |
| CS227697B2 (en) | 1984-05-14 |
| NO822526L (no) | 1983-02-25 |
| PH18343A (en) | 1985-06-05 |
| PT75241B (en) | 1984-08-02 |
| EP0073574A1 (en) | 1983-03-09 |
| FI822547A0 (fi) | 1982-07-20 |
| PT75241A (en) | 1982-08-01 |
| US4525202A (en) | 1985-06-25 |
| IL66226A0 (en) | 1982-11-30 |
| DK313582A (da) | 1983-02-25 |
| FI69848B (fi) | 1985-12-31 |
| FI822547L (fi) | 1983-02-25 |
| TR21496A (tr) | 1984-07-01 |
| GR77267B (da) | 1984-09-11 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| MM | Patent lapsed |
Owner name: STAUFFER CHEMICAL COMPANY |