DE2167051C2 - Erdalkalisalze von N-Phosphonomethylglycinen - Google Patents
Erdalkalisalze von N-PhosphonomethylglycinenInfo
- Publication number
- DE2167051C2 DE2167051C2 DE2167051A DE2167051A DE2167051C2 DE 2167051 C2 DE2167051 C2 DE 2167051C2 DE 2167051 A DE2167051 A DE 2167051A DE 2167051 A DE2167051 A DE 2167051A DE 2167051 C2 DE2167051 C2 DE 2167051C2
- Authority
- DE
- Germany
- Prior art keywords
- plants
- salts
- phosphonomethylglycine
- parts
- alkaline earth
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
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- 125000004218 chloromethyl group Chemical group [H]C([H])(Cl)* 0.000 description 1
- MOFCYHDQWIZKMY-UHFFFAOYSA-N chloromethylphosphonic acid Chemical class OP(O)(=O)CCl MOFCYHDQWIZKMY-UHFFFAOYSA-N 0.000 description 1
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- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 description 1
- 125000005131 dialkylammonium group Chemical group 0.000 description 1
- 229940117389 dichlorobenzene Drugs 0.000 description 1
- LXCYSACZTOKNNS-UHFFFAOYSA-N diethoxy(oxo)phosphanium Chemical compound CCO[P+](=O)OCC LXCYSACZTOKNNS-UHFFFAOYSA-N 0.000 description 1
- 150000005332 diethylamines Chemical class 0.000 description 1
- KCIDZIIHRGYJAE-YGFYJFDDSA-L dipotassium;[(2r,3r,4s,5r,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] phosphate Chemical class [K+].[K+].OC[C@H]1O[C@H](OP([O-])([O-])=O)[C@H](O)[C@@H](O)[C@H]1O KCIDZIIHRGYJAE-YGFYJFDDSA-L 0.000 description 1
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- 239000000839 emulsion Substances 0.000 description 1
- 150000002169 ethanolamines Chemical class 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- NTNZTEQNFHNYBC-UHFFFAOYSA-N ethyl 2-aminoacetate Chemical compound CCOC(=O)CN NTNZTEQNFHNYBC-UHFFFAOYSA-N 0.000 description 1
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- 125000004216 fluoromethyl group Chemical group [H]C([H])(F)* 0.000 description 1
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- 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
- 239000001257 hydrogen Substances 0.000 description 1
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- 239000012433 hydrogen halide Substances 0.000 description 1
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- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
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- 150000002576 ketones Chemical class 0.000 description 1
- 239000010871 livestock manure Substances 0.000 description 1
- QWDJLDTYWNBUKE-UHFFFAOYSA-L magnesium bicarbonate Chemical compound [Mg+2].OC([O-])=O.OC([O-])=O QWDJLDTYWNBUKE-UHFFFAOYSA-L 0.000 description 1
- 239000000395 magnesium oxide Substances 0.000 description 1
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 1
- 159000000003 magnesium salts Chemical class 0.000 description 1
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- 235000009973 maize Nutrition 0.000 description 1
- 229910052748 manganese Inorganic materials 0.000 description 1
- 239000011572 manganese Substances 0.000 description 1
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 1
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- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 1
- 229910052753 mercury Inorganic materials 0.000 description 1
- 125000006178 methyl benzyl group Chemical group 0.000 description 1
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- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 230000009526 moderate injury Effects 0.000 description 1
- 150000002780 morpholines Chemical class 0.000 description 1
- WMIPWRSVIZFVQB-UHFFFAOYSA-N n,n-dimethyl-2,2-diphenylacetamide Chemical compound C=1C=CC=CC=1C(C(=O)N(C)C)C1=CC=CC=C1.C=1C=CC=CC=1C(C(=O)N(C)C)C1=CC=CC=C1 WMIPWRSVIZFVQB-UHFFFAOYSA-N 0.000 description 1
- 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000001624 naphthyl group Chemical group 0.000 description 1
- 125000004998 naphthylethyl group Chemical group C1(=CC=CC2=CC=CC=C12)CC* 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- XITQUSLLOSKDTB-UHFFFAOYSA-N nitrofen Chemical compound C1=CC([N+](=O)[O-])=CC=C1OC1=CC=C(Cl)C=C1Cl XITQUSLLOSKDTB-UHFFFAOYSA-N 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 125000004433 nitrogen atom Chemical group N* 0.000 description 1
- 235000014571 nuts Nutrition 0.000 description 1
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000000962 organic group Chemical group 0.000 description 1
- 239000007800 oxidant agent Substances 0.000 description 1
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- 239000002245 particle Substances 0.000 description 1
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- 239000008188 pellet Substances 0.000 description 1
- 239000000575 pesticide Substances 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 125000006187 phenyl benzyl group Chemical group 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 125000000286 phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])* 0.000 description 1
- OJMIONKXNSYLSR-UHFFFAOYSA-N phosphorous acid Chemical compound OP(O)O OJMIONKXNSYLSR-UHFFFAOYSA-N 0.000 description 1
- 230000008832 photodamage Effects 0.000 description 1
- 231100000208 phytotoxic Toxicity 0.000 description 1
- 230000000885 phytotoxic effect Effects 0.000 description 1
- 150000003053 piperidines Chemical class 0.000 description 1
- 235000012015 potatoes Nutrition 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- WJNRPILHGGKWCK-UHFFFAOYSA-N propazine Chemical compound CC(C)NC1=NC(Cl)=NC(NC(C)C)=N1 WJNRPILHGGKWCK-UHFFFAOYSA-N 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 150000003222 pyridines Chemical class 0.000 description 1
- 235000013526 red clover Nutrition 0.000 description 1
- 235000009566 rice Nutrition 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- ODCWYMIRDDJXKW-UHFFFAOYSA-N simazine Chemical compound CCNC1=NC(Cl)=NC(NCC)=N1 ODCWYMIRDDJXKW-UHFFFAOYSA-N 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 239000002426 superphosphate Substances 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 239000000375 suspending agent Substances 0.000 description 1
- 239000003784 tall oil Substances 0.000 description 1
- 150000007970 thio esters Chemical class 0.000 description 1
- 150000003573 thiols Chemical class 0.000 description 1
- 125000003944 tolyl group Chemical group 0.000 description 1
- 125000005208 trialkylammonium group Chemical group 0.000 description 1
- 150000003918 triazines Chemical class 0.000 description 1
- 150000003852 triazoles Chemical class 0.000 description 1
- 150000003672 ureas Chemical class 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)]
- C07F9/3804—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
-
- 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
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Biochemistry (AREA)
- General Health & Medical Sciences (AREA)
- Molecular Biology (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US12305771A | 1971-03-10 | 1971-03-10 | |
US00170385A US3799758A (en) | 1971-08-09 | 1971-08-09 | N-phosphonomethyl-glycine phytotoxicant compositions |
Publications (2)
Publication Number | Publication Date |
---|---|
DE2167051B1 DE2167051B1 (de) | 1979-03-08 |
DE2167051C2 true DE2167051C2 (de) | 1979-10-31 |
Family
ID=26821180
Family Applications (3)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DE2152826A Expired DE2152826C3 (de) | 1971-03-10 | 1971-10-22 | Verwendung von N-Phosphonomethylglycinen und deren Salze als Herbizide |
DE2167051A Expired DE2167051C2 (de) | 1971-03-10 | 1971-10-22 | Erdalkalisalze von N-Phosphonomethylglycinen |
DE2166573A Expired DE2166573C3 (de) | 1971-03-10 | 1971-10-22 | N-Phosphonomethylglycin-Derivate und deren Salze |
Family Applications Before (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DE2152826A Expired DE2152826C3 (de) | 1971-03-10 | 1971-10-22 | Verwendung von N-Phosphonomethylglycinen und deren Salze als Herbizide |
Family Applications After (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DE2166573A Expired DE2166573C3 (de) | 1971-03-10 | 1971-10-22 | N-Phosphonomethylglycin-Derivate und deren Salze |
Country Status (31)
Families Citing this family (25)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB1436843A (en) * | 1972-07-21 | 1976-05-26 | Ici Ltd | Preparation of n-phosphonomethyl-glycine |
DE2717440C2 (de) * | 1976-05-17 | 1984-04-05 | Hoechst Ag, 6230 Frankfurt | Unkrautbekämpfung mit [(3-Amino-3-carboxy)-propyl-1]-methylphosphinsäure-Derivaten |
EG12897A (en) * | 1976-12-13 | 1980-07-31 | Monsanto Co | N,n,methylebebis-co,o-diaryl-n-phosphonomethylglycinonitrilles |
US4140513A (en) * | 1978-01-03 | 1979-02-20 | Monsanto Company | Sodium sesquiglyphosate |
DE2962495D1 (en) * | 1978-04-06 | 1982-05-27 | Monsanto Co | Derivatives of n-trifluoroacetyl n-phosphonomethylglycine dichloride, their preparation and their use as herbicides |
US4175946A (en) * | 1978-07-10 | 1979-11-27 | Monsanto Company | Thio derivatives of N-trifluoroacetyl-N-phosphonomethylglycine |
US4218235A (en) * | 1978-07-10 | 1980-08-19 | Monsanto Company | Ester derivatives of n-trifluoroacetyl-n-phosphonomethylglycine and the herbicidal use thereof |
US4359332A (en) * | 1978-07-10 | 1982-11-16 | Monsanto Company | Amide and hydrazide derivatives of N-trifluoroacetyl-N-phosphonomethylglycine as herbicides |
US4180394A (en) * | 1978-07-10 | 1979-12-25 | Monsanto Company | Derivatives of N-trifluoroacetyl-N-phosphonomethylglycinates and the herbicidal use thereof |
US4414158A (en) * | 1980-04-29 | 1983-11-08 | Ciba-Geigy Corporation | Phosphonomethylglycylhydroxamic acid and novel herbicidally active salts thereof |
ES8603901A1 (es) * | 1983-07-27 | 1986-01-01 | Rhone Poulenc Agrochimie | Procedimiento de preparacion de sulfonamidas con grupo ansinometilfosfonico |
DE3614788A1 (de) * | 1986-05-02 | 1987-11-05 | Hoechst Ag | Herbizide emulsionen |
FR2644036B1 (fr) * | 1989-03-07 | 1992-01-17 | Rhone Poulenc Agrochimie | Combine herbicide constitue d'un emballage polymere hydrosoluble et d'un herbicide contenant de la n-phosphonomethylglycine |
DE19528054A1 (de) * | 1995-07-31 | 1997-02-06 | Bayer Ag | Verfahren zur Herstellung von N-Phosphonomethylglycinestern |
DE19528060A1 (de) * | 1995-07-31 | 1997-02-06 | Bayer Ag | Verfahren zur Herstellung von N-Phosphonomethyl-glycinestern |
IL116695A0 (en) * | 1996-01-07 | 1996-05-14 | Yeda Res & Dev | Seed dressing compositions |
WO1997031534A1 (de) * | 1996-02-28 | 1997-09-04 | Bayer Aktiengesellschaft | Verwendung von n-phosphonomethyl-glycinestern in wässriger lösung als herbizide und neue n-phosphonomethyl-glycinester |
NZ550322A (en) | 2004-03-30 | 2012-02-24 | Monsanto Technology Llc | Methods for controlling plant pathogens using glyphosate |
DE102005026482A1 (de) | 2005-06-09 | 2006-12-14 | Bayer Cropscience Ag | Wirkstoffkombinationen |
WO2006131230A2 (de) | 2005-06-09 | 2006-12-14 | Bayer Cropscience Ag | Wirkstoffkombinationen |
RU2356229C2 (ru) * | 2007-05-10 | 2009-05-27 | Государственное учреждение "Научно-исследовательский технологический институт гербицидов и регуляторов роста растений с опытно-экспериментальным производством Академии наук Республики Башкортостан" | Гербицидное средство и способ его получения |
WO2010135324A1 (en) | 2009-05-18 | 2010-11-25 | Monsanto Technology Llc | Use of glyphosate for disease suppression and yield enhancement in soybean |
UA108623C2 (uk) | 2009-09-30 | 2015-05-25 | Низьколеткі амінні солі аніонних пестицидів | |
EP2460404A1 (en) | 2010-12-01 | 2012-06-06 | Basf Se | Compositions containing identical polyamine salts of mixed anionic pesticides |
US11109591B2 (en) | 2017-04-24 | 2021-09-07 | Taminco Bvba | Single phase liquids of alkanolamine salts of dicamba |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
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US3160632A (en) * | 1961-01-30 | 1964-12-08 | Stauffer Chemical Co | Aminomethylenephosphinic acids, salts thereof, and process for their production |
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1971
- 1971-10-11 PH PH12914A patent/PH16509A/en unknown
- 1971-10-15 SU SU711714528A patent/SU638238A3/ru active
- 1971-10-21 HU HU71MO810A patent/HU174479B/hu unknown
- 1971-10-21 NL NL717114487A patent/NL146171B/xx not_active IP Right Cessation
- 1971-10-21 ES ES396223A patent/ES396223A1/es not_active Expired
- 1971-10-22 IT IT30219/71A patent/IT946007B/it active
- 1971-10-22 NO NO3926/71A patent/NO141090C/no unknown
- 1971-10-22 DE DE2152826A patent/DE2152826C3/de not_active Expired
- 1971-10-22 IE IE1340/71A patent/IE35501B1/xx unknown
- 1971-10-22 OA OA54402A patent/OA03838A/xx unknown
- 1971-10-22 PT PT56642A patent/PT56642A1/pt unknown
- 1971-10-22 CH CH1539171A patent/CH571306A5/xx not_active IP Right Cessation
- 1971-10-22 DE DE2167051A patent/DE2167051C2/de not_active Expired
- 1971-10-22 SE SE7113473A patent/SE400695B/xx unknown
- 1971-10-22 DD DD160070A patent/DD100868A6/xx unknown
- 1971-10-22 ZM ZM150/71A patent/ZM15071A1/xx unknown
- 1971-10-22 CY CY837A patent/CY837A/xx unknown
- 1971-10-22 RO RO7168548A patent/RO72460A/ro unknown
- 1971-10-22 GB GB4926371A patent/GB1366379A/en not_active Expired
- 1971-10-22 DE DE2166573A patent/DE2166573C3/de not_active Expired
- 1971-10-22 TR TR18244A patent/TR18244A/xx unknown
- 1971-10-22 FI FI3000/71A patent/FI57955C/fi active
- 1971-10-22 BR BR7076/71A patent/BR7107076D0/pt unknown
- 1971-10-22 DK DK514071AA patent/DK140433B/da not_active IP Right Cessation
- 1971-10-22 JP JP8384671A patent/JPS566401B1/ja active Pending
- 1971-10-22 BG BG018842A patent/BG18585A3/xx unknown
- 1971-10-22 CA CA125905A patent/CA936865A/en not_active Expired
- 1971-10-22 IL IL47972A patent/IL47972A/en unknown
- 1971-10-22 RO RO7199872A patent/RO77018A/ro unknown
- 1971-10-22 IL IL37993A patent/IL37993A/en unknown
- 1971-10-22 YU YU02686/71A patent/YU36532B/xx unknown
- 1971-10-22 BE BE774349A patent/BE774349A/xx not_active IP Right Cessation
- 1971-10-22 FR FR7138086A patent/FR2129327A5/fr not_active Expired
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1972
- 1972-10-09 SU SU721834717A patent/SU665775A3/ru active
- 1972-10-09 SU SU721834717D patent/SU963446A3/ru active
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1974
- 1974-02-28 SE SE7402719A patent/SE400158B/xx not_active IP Right Cessation
- 1974-02-28 SE SE7402718A patent/SE399267B/xx not_active IP Right Cessation
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1975
- 1975-08-21 IL IL47972A patent/IL47972A0/xx unknown
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1976
- 1976-02-11 KE KE2599*UA patent/KE2599A/xx unknown
- 1976-12-30 MY MY110/76A patent/MY7600110A/xx unknown
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1979
- 1979-10-16 PH PH23177A patent/PH13752A/en unknown
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8381 | Inventor (new situation) |
Free format text: FRANZ, JOHN EDWARD, CRESTWOOD, MO., US |