PL92403B1 - - Google Patents
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- Publication number
- PL92403B1 PL92403B1 PL1974175344A PL17534474A PL92403B1 PL 92403 B1 PL92403 B1 PL 92403B1 PL 1974175344 A PL1974175344 A PL 1974175344A PL 17534474 A PL17534474 A PL 17534474A PL 92403 B1 PL92403 B1 PL 92403B1
- Authority
- PL
- Poland
- Prior art keywords
- phosphonomethylglycine
- combination
- effective amount
- herbicidally effective
- auxiliary additives
- Prior art date
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- 239000000203 mixture Substances 0.000 claims description 9
- 230000002363 herbicidal effect Effects 0.000 claims description 8
- XDDAORKBJWWYJS-UHFFFAOYSA-N glyphosate Chemical compound OC(=O)CNCP(O)(O)=O XDDAORKBJWWYJS-UHFFFAOYSA-N 0.000 claims description 4
- 239000004094 surface-active agent Substances 0.000 claims description 4
- 229910052783 alkali metal Inorganic materials 0.000 claims description 3
- 150000001340 alkali metals Chemical class 0.000 claims description 3
- 229910052784 alkaline earth metal Inorganic materials 0.000 claims description 3
- 150000001342 alkaline earth metals Chemical class 0.000 claims description 3
- 150000001875 compounds Chemical class 0.000 claims description 3
- 150000007530 organic bases Chemical class 0.000 claims description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims description 2
- 229910052739 hydrogen Inorganic materials 0.000 claims description 2
- 239000001257 hydrogen Substances 0.000 claims description 2
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims description 2
- JJWLVOIRVHMVIS-UHFFFAOYSA-N isopropylamine Chemical class CC(C)N JJWLVOIRVHMVIS-UHFFFAOYSA-N 0.000 claims description 2
- 239000000654 additive Substances 0.000 claims 3
- FBYFHODQAUBIOO-UHFFFAOYSA-N 2-(1-carboxyethoxy)propanoic acid Chemical compound OC(=O)C(C)OC(C)C(O)=O FBYFHODQAUBIOO-UHFFFAOYSA-N 0.000 claims 1
- 150000002148 esters Chemical class 0.000 claims 1
- 239000004480 active ingredient Substances 0.000 description 4
- 239000004009 herbicide Substances 0.000 description 4
- -1 N-ethylpropanolamine Chemical compound 0.000 description 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- 239000002585 base Substances 0.000 description 3
- 230000006378 damage Effects 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 2
- KDSNLYIMUZNERS-UHFFFAOYSA-N 2-methylpropanamine Chemical group CC(C)CN KDSNLYIMUZNERS-UHFFFAOYSA-N 0.000 description 2
- VVJKKWFAADXIJK-UHFFFAOYSA-N Allylamine Chemical compound NCC=C VVJKKWFAADXIJK-UHFFFAOYSA-N 0.000 description 2
- ROSDSFDQCJNGOL-UHFFFAOYSA-N Dimethylamine Chemical compound CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 description 2
- QUSNBJAOOMFDIB-UHFFFAOYSA-N Ethylamine Chemical group CCN QUSNBJAOOMFDIB-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
- HQABUPZFAYXKJW-UHFFFAOYSA-N butan-1-amine Chemical group CCCCN HQABUPZFAYXKJW-UHFFFAOYSA-N 0.000 description 2
- 125000004181 carboxyalkyl group Chemical group 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- BMFVGAAISNGQNM-UHFFFAOYSA-N isopentylamine Chemical group CC(C)CCN BMFVGAAISNGQNM-UHFFFAOYSA-N 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- WGYKZJWCGVVSQN-UHFFFAOYSA-N propylamine Chemical group CCCN WGYKZJWCGVVSQN-UHFFFAOYSA-N 0.000 description 2
- 238000005507 spraying Methods 0.000 description 2
- GETQZCLCWQTVFV-UHFFFAOYSA-N trimethylamine Chemical compound CN(C)C GETQZCLCWQTVFV-UHFFFAOYSA-N 0.000 description 2
- HXKKHQJGJAFBHI-UHFFFAOYSA-N 1-aminopropan-2-ol Chemical compound CC(O)CN HXKKHQJGJAFBHI-UHFFFAOYSA-N 0.000 description 1
- LJDSTRZHPWMDPG-UHFFFAOYSA-N 2-(butylamino)ethanol Chemical compound CCCCNCCO LJDSTRZHPWMDPG-UHFFFAOYSA-N 0.000 description 1
- BFSVOASYOCHEOV-UHFFFAOYSA-N 2-diethylaminoethanol Chemical compound CCN(CC)CCO BFSVOASYOCHEOV-UHFFFAOYSA-N 0.000 description 1
- WBIQQQGBSDOWNP-UHFFFAOYSA-N 2-dodecylbenzenesulfonic acid Chemical compound CCCCCCCCCCCCC1=CC=CC=C1S(O)(=O)=O WBIQQQGBSDOWNP-UHFFFAOYSA-N 0.000 description 1
- IIFFFBSAXDNJHX-UHFFFAOYSA-N 2-methyl-n,n-bis(2-methylpropyl)propan-1-amine Chemical compound CC(C)CN(CC(C)C)CC(C)C IIFFFBSAXDNJHX-UHFFFAOYSA-N 0.000 description 1
- SPVVMXMTSODFPU-UHFFFAOYSA-N 3-methyl-n-(3-methylbutyl)butan-1-amine Chemical compound CC(C)CCNCCC(C)C SPVVMXMTSODFPU-UHFFFAOYSA-N 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
- WJYIASZWHGOTOU-UHFFFAOYSA-N Heptylamine Chemical group CCCCCCCN WJYIASZWHGOTOU-UHFFFAOYSA-N 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- WUGQZFFCHPXWKQ-UHFFFAOYSA-N Propanolamine Chemical compound NCCCO WUGQZFFCHPXWKQ-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000013543 active substance Substances 0.000 description 1
- 150000003973 alkyl amines Chemical class 0.000 description 1
- 150000001414 amino alcohols Chemical class 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- 239000012736 aqueous medium Substances 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 239000007900 aqueous suspension Substances 0.000 description 1
- 229910052788 barium Inorganic materials 0.000 description 1
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 1
- 229910052790 beryllium Inorganic materials 0.000 description 1
- ATBAMAFKBVZNFJ-UHFFFAOYSA-N beryllium atom Chemical compound [Be] ATBAMAFKBVZNFJ-UHFFFAOYSA-N 0.000 description 1
- 229910052792 caesium Inorganic materials 0.000 description 1
- TVFDJXOCXUVLDH-UHFFFAOYSA-N caesium atom Chemical compound [Cs] TVFDJXOCXUVLDH-UHFFFAOYSA-N 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 229940125904 compound 1 Drugs 0.000 description 1
- 229940125782 compound 2 Drugs 0.000 description 1
- 229940126214 compound 3 Drugs 0.000 description 1
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 1
- HPNMFZURTQLUMO-UHFFFAOYSA-N diethylamine Chemical compound CCNCC HPNMFZURTQLUMO-UHFFFAOYSA-N 0.000 description 1
- LAWOZCWGWDVVSG-UHFFFAOYSA-N dioctylamine Chemical compound CCCCCCCCNCCCCCCCC LAWOZCWGWDVVSG-UHFFFAOYSA-N 0.000 description 1
- WEHWNAOGRSTTBQ-UHFFFAOYSA-N dipropylamine Chemical compound CCCNCCC WEHWNAOGRSTTBQ-UHFFFAOYSA-N 0.000 description 1
- WGBBUURBHXLGFM-UHFFFAOYSA-N hexan-2-amine Chemical group CCCCC(C)N WGBBUURBHXLGFM-UHFFFAOYSA-N 0.000 description 1
- 229940102253 isopropanolamine Drugs 0.000 description 1
- 150000002596 lactones Chemical class 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 125000000250 methylamino group Chemical group [H]N(*)C([H])([H])[H] 0.000 description 1
- 230000009526 moderate injury Effects 0.000 description 1
- BAVYZALUXZFZLV-UHFFFAOYSA-N mono-methylamine Natural products NC BAVYZALUXZFZLV-UHFFFAOYSA-N 0.000 description 1
- OOHAUGDGCWURIT-UHFFFAOYSA-N n,n-dipentylpentan-1-amine Chemical compound CCCCCN(CCCCC)CCCCC OOHAUGDGCWURIT-UHFFFAOYSA-N 0.000 description 1
- CYQYCASVINMDFD-UHFFFAOYSA-N n,n-ditert-butyl-2-methylpropan-2-amine Chemical compound CC(C)(C)N(C(C)(C)C)C(C)(C)C CYQYCASVINMDFD-UHFFFAOYSA-N 0.000 description 1
- NJWMENBYMFZACG-UHFFFAOYSA-N n-heptylheptan-1-amine Chemical compound CCCCCCCNCCCCCCC NJWMENBYMFZACG-UHFFFAOYSA-N 0.000 description 1
- PXSXRABJBXYMFT-UHFFFAOYSA-N n-hexylhexan-1-amine Chemical compound CCCCCCNCCCCCC PXSXRABJBXYMFT-UHFFFAOYSA-N 0.000 description 1
- JACMPVXHEARCBO-UHFFFAOYSA-N n-pentylpentan-1-amine Chemical compound CCCCCNCCCCC JACMPVXHEARCBO-UHFFFAOYSA-N 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- FJDUDHYHRVPMJZ-UHFFFAOYSA-N nonan-1-amine Chemical group CCCCCCCCCN FJDUDHYHRVPMJZ-UHFFFAOYSA-N 0.000 description 1
- IOQPZZOEVPZRBK-UHFFFAOYSA-N octan-1-amine Chemical group CCCCCCCCN IOQPZZOEVPZRBK-UHFFFAOYSA-N 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- DPBLXKKOBLCELK-UHFFFAOYSA-N pentan-1-amine Chemical group CCCCCN DPBLXKKOBLCELK-UHFFFAOYSA-N 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- AOHJOMMDDJHIJH-UHFFFAOYSA-N propylenediamine Chemical compound CC(N)CN AOHJOMMDDJHIJH-UHFFFAOYSA-N 0.000 description 1
- 229910052701 rubidium Inorganic materials 0.000 description 1
- IGLNJRXAVVLDKE-UHFFFAOYSA-N rubidium atom Chemical compound [Rb] IGLNJRXAVVLDKE-UHFFFAOYSA-N 0.000 description 1
- 230000009528 severe injury Effects 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 239000008247 solid mixture Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 229910052712 strontium Inorganic materials 0.000 description 1
- CIOAGBVUUVVLOB-UHFFFAOYSA-N strontium atom Chemical compound [Sr] CIOAGBVUUVVLOB-UHFFFAOYSA-N 0.000 description 1
- 239000003760 tallow Substances 0.000 description 1
- YBRBMKDOPFTVDT-UHFFFAOYSA-N tert-butylamine Chemical group CC(C)(C)N YBRBMKDOPFTVDT-UHFFFAOYSA-N 0.000 description 1
- IMFACGCPASFAPR-UHFFFAOYSA-N tributylamine Chemical compound CCCCN(CCCC)CCCC IMFACGCPASFAPR-UHFFFAOYSA-N 0.000 description 1
- RKBCYCFRFCNLTO-UHFFFAOYSA-N triisopropylamine Chemical compound CC(C)N(C(C)C)C(C)C RKBCYCFRFCNLTO-UHFFFAOYSA-N 0.000 description 1
- YFTHZRPMJXBUME-UHFFFAOYSA-N tripropylamine Chemical compound CCCN(CCC)CCC YFTHZRPMJXBUME-UHFFFAOYSA-N 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
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)
- Cosmetics (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
Przedmiotem wynalazku jest srodek chwastobój¬ czy, zawierajacy jako substancje czynna nowe estry karboksyalkilowe N-fosfonometyloglicyny, ewentualnie w postaci soli.Nowe estry karboksyalkilowe stanowiace sub¬ stancje czynna srodka wedlug wynalazku maja wzór przedstawiony na rysunku, w którym M, M' i M" oznaczaja niezaleznie od siebie atom wodo¬ ru, atom metalu alkalicznego lub metalu ziem al¬ kalicznych, kation amoniowy albo zasade organicz¬ na.Estry karboksyalkilowe otrzymuje sie w reakcji N-fosfonometyloglicyny w srodowisku wodnym z laktonem, takim jak proplolakton, w obecnosci zasady. Po zobojetnieniu zasady kwasem solnym otrzymuje sie wolny kwas, z którego w reakcji z róznymi zasadami otrzymuje sie rozmaite sole.Okreslenie „metale alkaliczne" dotyczy litu, so¬ du, potasu, cezu i rubidu. Okreslenie „metale ziem alkalicznych" dotyczy berylu, magnezu, wapnia, strontu i baru.Sole z zasadami organicznymi otrzymuje sie w reakcji z aminami o ciezarze czasteczkowym nie przekraczajacym okolo 300. Do takich amin nale¬ za: alkiloaminy, alkilenoaminy i aminoalkohole za¬ wierajace nie wiecej niz dwie grupy aminowe, ta¬ kie jak metyloamina, etyloamina, n-propyloamina, izoprbpyloamina, n-butyloamina, izobutyloamina, Il-rz.-butyloamina, n-amyloamina, izoamyloamina, 2 heksyloamina, heptyloamina, oktyloamina, nonylo- amina^ decyloamina, pentadecyloamina, heksadecy- loamina, heptadecyloamina, oktadecyloamina, ety- lobutyloamina, etyloheptyloamina, undecyloamina, dodecyloamina, tridecyloamina, tetradecyloamina, metyloetyloamina, metyloizopropyloamina, metylo- heksyloamina, metylononyloamina, metylopentade- cyloamina, metylooktadecyloamina, etylooktyloa- mina, heksyloheptyloamina, heksylooktyloamina, dwumetyloamina, dwuetyloamina, dwu-n-propylo- amina, dwu-n-amyloamina, dwuizoamyloamina, dwuheksyloamina, dwuheptyloamina, dwuoktylo- amina, trójmetyloamina, trójetyloamina, trój-n-pro- pyloamina, trójizopropyloamina, trój-n-butyloami¬ na, trój izobutyloamina, trój-II-rz.-butyloamina, trój-n-amyloamina, etanoloamina, n-propanoloami- na, izopropanoloamina, dwuetanoloamina, N, N- -dwuetyloetanoloamina, N-etylopropanoloamina, N-butyloetanoloamina, alliloamina, n-butenylo-2- -amina, n-pentenylo-2-amina, 2, 3-dwumetylobute- nylo-2-amina, dwubutenylo-2-amina, n-heksenylo- -2-amina oraz propylenodwuamina.Srodek chwastobójczy wedlug wynalazku zawie¬ ra substancje czynna w polaczeniu z jednym lub wiecej adjuwentami, do których naleza nosniki, rozcienczalniki, srodki do kondycjonowania i po¬ dobne i moze byc formowany w postaci takie, jak zwilzalne proszki, zawiesiny wodne, preparaty py^ liste, oleje do sporzadzania emulsji i roztwory w rozpuszczalnikach. Z reguly w sklad kompozycji 92 4033 92 403 4 wchodzi takze jeden lub wiecej srodków po¬ wierzchniowo czynnych.Srodki powierzchniowo czynne, stosowane do sporzadzania srodków chwastobójczych, sa znane i opisane w opisach patentowych Stanów Zjedno¬ czonych Ameryki, biuletynach i monografiach.Zawartosc skladnika aktywnego w srodku chwa¬ stobójczym wedlug wynalazku wynosi zwykle 0,5—95 czesci wagowych na 100 czesci zwilzamyeh proszków lub preparatów pylistych. Znajacy zagad¬ nienie moga z latwoscia sporzadzac kompozycje za¬ wierajace inne niz podane ilosci skladnika aktyw¬ nego.Sposób zastosowania srodka chwastobójczego wedlug wynalazku jest dobrze znany. Ciekla, a w szczególnosci stale kompozycje mozna podawac do czesci nadziemnych roslin stosujac zwykle sposoby, np. za pomoca mechanicznych rozpylaczy luib me¬ chanicznych albo recznych opryskiwaczy. Dla uzy¬ skania normalnego efektu chwastobójczego mie¬ szanki chwastobójcze stosuje sie w ilosci 2,5—125 czesci wagowych na hektar, w przeliczeniu na sub¬ stancje czynna.Przyklad. Aktywnosc chwastobójcza po wzror scie roslin, zwiazków stanowiacych substancje czynna srodka wedlug wynalazku, sprawdzono w nastepujacy spoisób. Stosowano srodek w postaci preparatu do opryskiwania 14_ lub 21-dniowych sadzonek róznych roslin! Jako preparat do opryski¬ wania stosowano wodny roztwór skladnika aktyw¬ nego zawierajacy srodek powierzchniowo czynny skladajacy sie z 35 czesci soli butyloamoniowej kwa¬ su dodecylobenzenosulfonowego oraz 65 czesci oleju lojowego skondensowanego z tlenkiem etylenu w stosunku molarnym 11:1. Preparat stosowano do roslin w róznych stadiach rozwoju i w róznych dawkach. Rosliny po opryskaniu hodowano w szklarni i obserwowano skutki dzialania preparatu po okolo 2 lub okolo 4 tygodniach. Wyniki przed¬ stawiono w tablicy1. v W tablicy 1 przyjeto nastepujace oznaczenia skutków dzialania srodka chwastobójczego.Wynik Brak uszkodzen Lekkie uszkodzenie Umiarkowane uszkodzenie Powazne uszkodzenie Calkowite zniszczenie Oznaczenie 0 1 2 3 4 Tablica 1 Zwia¬ zek Dawka kg/ha N cd o cd cd s cd W cd o 3 H cd 'cd 'O cd I cd fi o 3 cd cd s ta M o O N -t» O CO ,Q ¦g S i-i O. 1 2 • 3 4,46 11,2 4,46 11,2 4,46 — — 3 3 1 1 2 3 2 2 1 1 3 3 1 1 2 2 1 1 0 0 2 3 1 1 2 2 2 2 1 1 2 3 2 2 2 2 2 2 3 3 3 3 3 4 2 3 2 2 0 0 — — 2 2 0 0 1 2 0 0 1 2 0 0 2 2 0 0 1 1 1 2 0 0 0 1 0 1 0 0 2 2 1 0 2 3 1 1 0 1 2 3 0 0 2 3 1 1 3 3 2 3 1 2 3 3 2 3 2 4 2 4 2 4 2 4 2 4 Zwiazek 1 — ester 2^karboksyetylowy N-fosfono¬ metyloglicyny Zwiazek 2 — sól dwuizopropyloaminowa estru 2-kariboksyetylowego N-fosfonomety¬ loglicyny Zwiazek 3 — sól dwusodowa estru 2-karboksyety- lowego N-fosfonometylogliicyny PL PL PL
Claims (3)
1. Zastrzezenia patentowe 1. Srodek chwastobójczy, znamienny tym, ze za¬ wiera skuteczna chwastobójczo ilosc zwiazku o wzorze przedstawionym na rysunku, w którym M, M' i M" oznaczaja niezaleznie od siebie atom 55 wodoru, atom metalu alkalicznego lub metalu ziem alkalicznych, kation amoniowy lub zasade organicz¬ na w polaczeniu z dodatkami pomocniczymi oraz dodatkowo srodek powierzchniowo czynny.
2. Srodek wedlug zastrz. 1, znamienny tym, ze zawiera skuteczna chwastobójczo lilosc eteru jl-kar- boksyetylowego N-fosfonometyloglicyny w polacze¬ niu z dodatkami pomocniczymi.
3. Srodek wedlug zastrz. 1, znamienny tym, ze zawiera skuteczna chwastobójczo ilosc soli jedno- izopropyloaminowej estru p-karboksyetylowego N-fosfonometyloglicyny w polaczeniu z dodatkami pomocniczymi.92 403 M' \ O \0 H 0 O P-CH2-N-CH2C-0-(CH2)2-C- 0 / M" PL PL PL
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US417858A US3868407A (en) | 1973-11-21 | 1973-11-21 | Carboxyalkyl esters of n-phosphonomethyl glycine |
Publications (1)
Publication Number | Publication Date |
---|---|
PL92403B1 true PL92403B1 (pl) | 1977-04-30 |
Family
ID=23655654
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PL1974187852A PL93298B1 (pl) | 1973-11-21 | 1974-11-05 | |
PL1974175344A PL92403B1 (pl) | 1973-11-21 | 1974-11-05 |
Family Applications Before (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PL1974187852A PL93298B1 (pl) | 1973-11-21 | 1974-11-05 |
Country Status (31)
Country | Link |
---|---|
US (1) | US3868407A (pl) |
JP (1) | JPS5242854B2 (pl) |
AR (1) | AR219688A1 (pl) |
AT (1) | AT341267B (pl) |
BE (1) | BE821879A (pl) |
BG (1) | BG26183A3 (pl) |
BR (1) | BR7409238A (pl) |
CA (1) | CA1048053A (pl) |
CH (1) | CH593013A5 (pl) |
CS (1) | CS178935B2 (pl) |
DD (2) | DD121596A5 (pl) |
DE (1) | DE2452460C3 (pl) |
DK (1) | DK139360B (pl) |
EG (1) | EG11241A (pl) |
ES (1) | ES431614A1 (pl) |
FI (1) | FI60020C (pl) |
FR (1) | FR2251569B1 (pl) |
GB (1) | GB1440847A (pl) |
HU (1) | HU171312B (pl) |
IL (1) | IL45989A (pl) |
IN (1) | IN140421B (pl) |
IT (1) | IT1049325B (pl) |
NL (1) | NL172065C (pl) |
NO (1) | NO143747C (pl) |
PH (1) | PH10683A (pl) |
PL (2) | PL93298B1 (pl) |
RO (1) | RO72710A (pl) |
SE (1) | SE421625B (pl) |
SU (1) | SU682097A3 (pl) |
YU (1) | YU40107B (pl) |
ZA (1) | ZA747107B (pl) |
Families Citing this family (23)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3988142A (en) * | 1972-02-03 | 1976-10-26 | Monsanto Company | Increasing carbohydrate deposition in plants with N-phosphono-methylglycine and derivatives thereof |
US3948975A (en) * | 1974-08-05 | 1976-04-06 | Monsanto Company | Hydroxyalkyl esters of N-phosphonomethyl glycine |
US4197254A (en) * | 1976-05-03 | 1980-04-08 | Monsanto Company | Derivatives of N-phosphonomethylglycine |
US4159901A (en) * | 1977-05-16 | 1979-07-03 | Monsanto Company | Corrosion inhibited agricultural compositions |
JPS5839127B2 (ja) * | 1978-03-09 | 1983-08-27 | 明治製菓株式会社 | 除草剤組成物 |
US4226610A (en) * | 1978-04-15 | 1980-10-07 | Meiji Selka Kaisha, Ltd. | Herbicidal compounds, preparation thereof and herbicides containing the same |
WO1984003607A1 (en) * | 1983-03-16 | 1984-09-27 | Chevron Res | Glyphosate-type herbicidal compositions |
ES534413A0 (es) * | 1983-07-27 | 1986-01-01 | Rhone Poulenc Agrochimie | Procedimiento de preparacion de sulfonamidas con grupo ansinometilfosfonico |
JPS60185443U (ja) * | 1984-05-21 | 1985-12-09 | 温泉青果農業協同組合 | 収穫用鋏 |
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 |
US5047079A (en) * | 1986-08-18 | 1991-09-10 | Ici Americas Inc. | Method of preparation and use of solid, phytoactive compositions |
FR2635522B1 (fr) * | 1988-08-18 | 1990-11-16 | Rhone Poulenc Agrochimie | N-sulfonomethylglycinate procede de preparation, utilisation dans la preparation d'herbicides de type glyphosate |
US5187292A (en) * | 1988-08-18 | 1993-02-16 | Rhone-Poulenc Agrochimie | N-sulfomethylglycinate, use in the preparation of herbicides of the glyphosate type |
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 |
HU212802B (en) | 1991-07-19 | 1996-11-28 | Monsanto Europe Sa | Phytoactive sack-like composition containing glyphosate-izopropylamine salt |
AU1790697A (en) * | 1996-02-28 | 1997-09-16 | Bayer Aktiengesellschaft | Use of n-phosphonomethylglycine esters in aqueous solution as herbicides, and new n-phosphonomethylglycine esters |
ITTO980048A1 (it) * | 1998-01-20 | 1999-07-20 | Ipici Spa | Composizioni erbicide, procedimenti per la loro preparazione ed impieghi |
US6921834B2 (en) | 2002-05-22 | 2005-07-26 | Dow Agrosciences Llc | Continuous process for preparing N-phosphonomethyl glycine |
AR037559A1 (es) * | 2002-11-19 | 2004-11-17 | Atanor S A | Una formulacion herbicida solida de n-fosfonometilglicina, bajo la forma de polvo, granulos o escamas, soluble o dispersable en agua, y el procedimiento para preparar dicha composicion |
US8470741B2 (en) * | 2003-05-07 | 2013-06-25 | Croda Americas Llc | Homogeneous liquid saccharide and oil systems |
ATE542425T1 (de) * | 2004-09-17 | 2012-02-15 | Monsanto Technology Llc | Glyphosate-formulierungen mit früh auftretenden verbrennungssymptomen |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3799758A (en) * | 1971-08-09 | 1974-03-26 | Monsanto Co | N-phosphonomethyl-glycine phytotoxicant compositions |
-
1973
- 1973-11-21 US US417858A patent/US3868407A/en not_active Expired - Lifetime
-
1974
- 1974-11-04 ES ES431614A patent/ES431614A1/es not_active Expired
- 1974-11-04 NL NLAANVRAGE7414338,A patent/NL172065C/xx not_active IP Right Cessation
- 1974-11-04 SU SU742076318A patent/SU682097A3/ru active
- 1974-11-04 IL IL45989A patent/IL45989A/en unknown
- 1974-11-05 FI FI3227/74A patent/FI60020C/fi active
- 1974-11-05 BG BG7428118A patent/BG26183A3/xx unknown
- 1974-11-05 PL PL1974187852A patent/PL93298B1/pl unknown
- 1974-11-05 CA CA212,996A patent/CA1048053A/en not_active Expired
- 1974-11-05 DD DD189587A patent/DD121596A5/xx unknown
- 1974-11-05 RO RO7480433A patent/RO72710A/ro unknown
- 1974-11-05 JP JP49126653A patent/JPS5242854B2/ja not_active Expired
- 1974-11-05 FR FR7436746A patent/FR2251569B1/fr not_active Expired
- 1974-11-05 IT IT29129/74A patent/IT1049325B/it active
- 1974-11-05 HU HU74MO00000919A patent/HU171312B/hu unknown
- 1974-11-05 IN IN2419/CAL/1974A patent/IN140421B/en unknown
- 1974-11-05 BR BR9238/74A patent/BR7409238A/pt unknown
- 1974-11-05 DK DK575274AA patent/DK139360B/da not_active IP Right Cessation
- 1974-11-05 PL PL1974175344A patent/PL92403B1/pl unknown
- 1974-11-05 DE DE2452460A patent/DE2452460C3/de not_active Expired
- 1974-11-05 YU YU2949/74A patent/YU40107B/xx unknown
- 1974-11-05 DD DD182166A patent/DD115686A5/xx unknown
- 1974-11-05 ZA ZA00747107A patent/ZA747107B/xx unknown
- 1974-11-05 SE SE7413853A patent/SE421625B/xx not_active IP Right Cessation
- 1974-11-05 CH CH1476974A patent/CH593013A5/xx not_active IP Right Cessation
- 1974-11-05 NO NO743973A patent/NO143747C/no unknown
- 1974-11-05 GB GB4783174A patent/GB1440847A/en not_active Expired
- 1974-11-05 AR AR256392A patent/AR219688A1/es active
- 1974-11-05 CS CS7400007541A patent/CS178935B2/cs unknown
- 1974-11-05 BE BE150233A patent/BE821879A/xx not_active IP Right Cessation
- 1974-11-05 AT AT884674A patent/AT341267B/de not_active IP Right Cessation
- 1974-11-08 PH PH16494A patent/PH10683A/en unknown
- 1974-11-20 EG EG515/74A patent/EG11241A/xx active
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