DE2856260A1 - Herbicide - Google Patents
HerbicideInfo
- Publication number
- DE2856260A1 DE2856260A1 DE19782856260 DE2856260A DE2856260A1 DE 2856260 A1 DE2856260 A1 DE 2856260A1 DE 19782856260 DE19782856260 DE 19782856260 DE 2856260 A DE2856260 A DE 2856260A DE 2856260 A1 DE2856260 A1 DE 2856260A1
- Authority
- DE
- Germany
- Prior art keywords
- acid
- salt
- ampb
- herbicidal composition
- composition according
- 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.)
- Ceased
Links
- 239000004009 herbicide Substances 0.000 title claims description 33
- 230000002363 herbicidal effect Effects 0.000 title claims description 28
- 241000196324 Embryophyta Species 0.000 claims description 69
- 150000001875 compounds Chemical class 0.000 claims description 52
- 239000000203 mixture Substances 0.000 claims description 50
- 150000003839 salts Chemical class 0.000 claims description 39
- 239000002253 acid Substances 0.000 claims description 11
- XDDAORKBJWWYJS-UHFFFAOYSA-N glyphosate Chemical compound OC(=O)CNCP(O)(O)=O XDDAORKBJWWYJS-UHFFFAOYSA-N 0.000 claims description 10
- 239000005631 2,4-Dichlorophenoxyacetic acid Substances 0.000 claims description 8
- OEYIOHPDSNJKLS-UHFFFAOYSA-N choline Chemical compound C[N+](C)(C)CCO OEYIOHPDSNJKLS-UHFFFAOYSA-N 0.000 claims description 7
- 229960001231 choline Drugs 0.000 claims description 7
- ROSDSFDQCJNGOL-UHFFFAOYSA-N Dimethylamine Chemical compound CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 claims description 6
- BGRDGMRNKXEXQD-UHFFFAOYSA-N Maleic hydrazide Chemical compound OC1=CC=C(O)N=N1 BGRDGMRNKXEXQD-UHFFFAOYSA-N 0.000 claims description 6
- 125000005210 alkyl ammonium group Chemical group 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
- XKJMBINCVNINCA-UHFFFAOYSA-N Alfalone Chemical compound CON(C)C(=O)NC1=CC=C(Cl)C(Cl)=C1 XKJMBINCVNINCA-UHFFFAOYSA-N 0.000 claims description 4
- 239000004381 Choline salt Substances 0.000 claims description 4
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical group [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 claims description 4
- 235000019417 choline salt Nutrition 0.000 claims description 4
- JJWLVOIRVHMVIS-UHFFFAOYSA-O isopropylaminium Chemical compound CC(C)[NH3+] JJWLVOIRVHMVIS-UHFFFAOYSA-O 0.000 claims description 4
- 150000003248 quinolines Chemical class 0.000 claims description 4
- 229910052708 sodium Inorganic materials 0.000 claims description 4
- HXKWSTRRCHTUEC-UHFFFAOYSA-N 2,4-Dichlorophenoxyaceticacid Chemical compound OC(=O)C(Cl)OC1=CC=C(Cl)C=C1 HXKWSTRRCHTUEC-UHFFFAOYSA-N 0.000 claims description 3
- KLSJWNVTNUYHDU-UHFFFAOYSA-N Amitrole Chemical compound NC1=NC=NN1 KLSJWNVTNUYHDU-UHFFFAOYSA-N 0.000 claims description 3
- 239000005983 Maleic hydrazide Substances 0.000 claims description 3
- 125000004429 atom Chemical group 0.000 claims description 3
- HQABUPZFAYXKJW-UHFFFAOYSA-N butan-1-amine Chemical compound CCCCN HQABUPZFAYXKJW-UHFFFAOYSA-N 0.000 claims description 3
- QZXCCPZJCKEPSA-UHFFFAOYSA-N chlorfenac Chemical compound OC(=O)CC1=C(Cl)C=CC(Cl)=C1Cl QZXCCPZJCKEPSA-UHFFFAOYSA-N 0.000 claims description 3
- 150000002148 esters Chemical class 0.000 claims description 3
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 3
- 229910052751 metal Inorganic materials 0.000 claims description 3
- 239000002184 metal Substances 0.000 claims description 3
- NPMSHBWDMYIJBG-UHFFFAOYSA-N phosphono n-ethylcarbamate Chemical compound CCNC(=O)OP(O)(O)=O NPMSHBWDMYIJBG-UHFFFAOYSA-N 0.000 claims description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims description 2
- 150000001558 benzoic acid derivatives Chemical class 0.000 claims description 2
- 238000000034 method Methods 0.000 claims description 2
- GSEJCLTVZPLZKY-UHFFFAOYSA-O triethanolammonium Chemical compound OCC[NH+](CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-O 0.000 claims description 2
- 244000052616 bacterial pathogen Species 0.000 claims 1
- 125000004436 sodium atom Chemical group 0.000 claims 1
- 230000002401 inhibitory effect Effects 0.000 description 20
- 230000002147 killing effect Effects 0.000 description 15
- 230000000694 effects Effects 0.000 description 14
- -1 polyoxyethylene octylphenyl ether Polymers 0.000 description 14
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 12
- 159000000000 sodium salts Chemical class 0.000 description 12
- 241000218691 Cupressaceae Species 0.000 description 11
- 229920002114 octoxynol-9 Polymers 0.000 description 11
- 238000009472 formulation Methods 0.000 description 9
- 239000000243 solution Substances 0.000 description 9
- 239000007921 spray Substances 0.000 description 9
- 239000004094 surface-active agent Substances 0.000 description 9
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 9
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 8
- 240000007113 Rumex obtusifolius Species 0.000 description 8
- 235000009422 Rumex obtusifolius Nutrition 0.000 description 8
- 239000005562 Glyphosate Substances 0.000 description 7
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 7
- 229940097068 glyphosate Drugs 0.000 description 7
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 6
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 6
- KEAYESYHFKHZAL-UHFFFAOYSA-N Sodium Chemical class [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 6
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 6
- 241000219053 Rumex Species 0.000 description 5
- 238000002360 preparation method Methods 0.000 description 5
- 230000001629 suppression Effects 0.000 description 5
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 4
- 241001070941 Castanea Species 0.000 description 4
- 235000014036 Castanea Nutrition 0.000 description 4
- 102000004190 Enzymes Human genes 0.000 description 4
- 108090000790 Enzymes Proteins 0.000 description 4
- 241000878006 Miscanthus sinensis Species 0.000 description 4
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 4
- 244000184734 Pyrus japonica Species 0.000 description 4
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 4
- DTQVDTLACAAQTR-UHFFFAOYSA-N Trifluoroacetic acid Chemical compound OC(=O)C(F)(F)F DTQVDTLACAAQTR-UHFFFAOYSA-N 0.000 description 4
- 235000011054 acetic acid Nutrition 0.000 description 4
- VLTRZXGMWDSKGL-UHFFFAOYSA-N perchloric acid Chemical compound OCl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-N 0.000 description 4
- 230000001850 reproductive effect Effects 0.000 description 4
- XZIDTOHMJBOSOX-UHFFFAOYSA-N 2,3,6-TBA Chemical compound OC(=O)C1=C(Cl)C=CC(Cl)=C1Cl XZIDTOHMJBOSOX-UHFFFAOYSA-N 0.000 description 3
- BIPAGODSEBNAJR-UHFFFAOYSA-N 2-(3,4-dichlorophenoxy)propanoic acid Chemical compound OC(=O)C(C)OC1=CC=C(Cl)C(Cl)=C1 BIPAGODSEBNAJR-UHFFFAOYSA-N 0.000 description 3
- LLWADFLAOKUBDR-UHFFFAOYSA-N 2-methyl-4-chlorophenoxybutyric acid Chemical compound CC1=CC(Cl)=CC=C1OCCCC(O)=O LLWADFLAOKUBDR-UHFFFAOYSA-N 0.000 description 3
- 235000017519 Artemisia princeps Nutrition 0.000 description 3
- 244000065027 Artemisia princeps Species 0.000 description 3
- HSSBORCLYSCBJR-UHFFFAOYSA-N Chloramben Chemical compound NC1=CC(Cl)=CC(C(O)=O)=C1Cl HSSBORCLYSCBJR-UHFFFAOYSA-N 0.000 description 3
- 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 3
- 240000007594 Oryza sativa Species 0.000 description 3
- 235000007164 Oryza sativa Nutrition 0.000 description 3
- 241000981595 Zoysia japonica Species 0.000 description 3
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 3
- 150000001413 amino acids Chemical class 0.000 description 3
- 125000004432 carbon atom Chemical group C* 0.000 description 3
- 150000005332 diethylamines Chemical class 0.000 description 3
- 238000011156 evaluation Methods 0.000 description 3
- 230000035784 germination Effects 0.000 description 3
- 229940093915 gynecological organic acid Drugs 0.000 description 3
- 230000005764 inhibitory process Effects 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 244000005700 microbiome Species 0.000 description 3
- 150000007522 mineralic acids Chemical class 0.000 description 3
- 239000002420 orchard Substances 0.000 description 3
- 150000007524 organic acids Chemical class 0.000 description 3
- 235000005985 organic acids Nutrition 0.000 description 3
- 229910052700 potassium Inorganic materials 0.000 description 3
- 239000011591 potassium Substances 0.000 description 3
- 235000019260 propionic acid Nutrition 0.000 description 3
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 3
- 235000009566 rice Nutrition 0.000 description 3
- 239000011734 sodium Substances 0.000 description 3
- 238000009331 sowing Methods 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- 230000005945 translocation Effects 0.000 description 3
- WNTGYJSOUMFZEP-UHFFFAOYSA-N 2-(4-chloro-2-methylphenoxy)propanoic acid Chemical compound OC(=O)C(C)OC1=CC=C(Cl)C=C1C WNTGYJSOUMFZEP-UHFFFAOYSA-N 0.000 description 2
- BMYNFMYTOJXKLE-UHFFFAOYSA-N 3-azaniumyl-2-hydroxypropanoate Chemical compound NCC(O)C(O)=O BMYNFMYTOJXKLE-UHFFFAOYSA-N 0.000 description 2
- 241000922659 Anisocampium niponicum Species 0.000 description 2
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 2
- 240000002779 Cayratia japonica Species 0.000 description 2
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 2
- 240000005109 Cryptomeria japonica Species 0.000 description 2
- 244000075634 Cyperus rotundus Species 0.000 description 2
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 description 2
- ZLSWBLPERHFHIS-UHFFFAOYSA-N Fenoprop Chemical compound OC(=O)C(C)OC1=CC(Cl)=C(Cl)C=C1Cl ZLSWBLPERHFHIS-UHFFFAOYSA-N 0.000 description 2
- 240000007171 Imperata cylindrica Species 0.000 description 2
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 2
- 239000005574 MCPA Substances 0.000 description 2
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 2
- BAVYZALUXZFZLV-UHFFFAOYSA-O Methylammonium ion Chemical compound [NH3+]C BAVYZALUXZFZLV-UHFFFAOYSA-O 0.000 description 2
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 2
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 2
- 244000046146 Pueraria lobata Species 0.000 description 2
- 235000010575 Pueraria lobata Nutrition 0.000 description 2
- 241001480065 Quercus serrata Species 0.000 description 2
- 244000233588 Rhododendron kaempferi Species 0.000 description 2
- 235000001507 Rhododendron kaempferi Nutrition 0.000 description 2
- 235000003966 Rubus morifolius Nutrition 0.000 description 2
- 244000111494 Rubus morifolius Species 0.000 description 2
- 241000544422 Sasa nipponica Species 0.000 description 2
- 235000008423 Solanum carolinense Nutrition 0.000 description 2
- 241000501039 Solanum carolinense Species 0.000 description 2
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 description 2
- WHKUVVPPKQRRBV-UHFFFAOYSA-N Trasan Chemical compound CC1=CC(Cl)=CC=C1OCC(O)=O WHKUVVPPKQRRBV-UHFFFAOYSA-N 0.000 description 2
- 240000001717 Vaccinium macrocarpon Species 0.000 description 2
- 241001464837 Viridiplantae Species 0.000 description 2
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 2
- 235000010323 ascorbic acid Nutrition 0.000 description 2
- 239000011668 ascorbic acid Substances 0.000 description 2
- 229960005070 ascorbic acid Drugs 0.000 description 2
- OTSAMNSACVKIOJ-UHFFFAOYSA-N azane;carbamoyl(ethoxy)phosphinic acid Chemical compound [NH4+].CCOP([O-])(=O)C(N)=O OTSAMNSACVKIOJ-UHFFFAOYSA-N 0.000 description 2
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 2
- 230000004071 biological effect Effects 0.000 description 2
- 239000011575 calcium Substances 0.000 description 2
- 229910052791 calcium Inorganic materials 0.000 description 2
- BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical compound OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 description 2
- FOCAUTSVDIKZOP-UHFFFAOYSA-N chloroacetic acid Chemical compound OC(=O)CCl FOCAUTSVDIKZOP-UHFFFAOYSA-N 0.000 description 2
- 229940106681 chloroacetic acid Drugs 0.000 description 2
- 235000015165 citric acid Nutrition 0.000 description 2
- 229910052802 copper Inorganic materials 0.000 description 2
- 239000010949 copper Substances 0.000 description 2
- IWEDIXLBFLAXBO-UHFFFAOYSA-N dicamba Chemical compound COC1=C(Cl)C=CC(Cl)=C1C(O)=O IWEDIXLBFLAXBO-UHFFFAOYSA-N 0.000 description 2
- HPNMFZURTQLUMO-UHFFFAOYSA-N diethylamine Chemical compound CCNCC HPNMFZURTQLUMO-UHFFFAOYSA-N 0.000 description 2
- 125000004494 ethyl ester group Chemical group 0.000 description 2
- QUSNBJAOOMFDIB-UHFFFAOYSA-O ethylaminium Chemical compound CC[NH3+] QUSNBJAOOMFDIB-UHFFFAOYSA-O 0.000 description 2
- 235000013305 food Nutrition 0.000 description 2
- 229910052744 lithium Inorganic materials 0.000 description 2
- 239000011777 magnesium Substances 0.000 description 2
- 229910052749 magnesium Inorganic materials 0.000 description 2
- 235000010270 methyl p-hydroxybenzoate Nutrition 0.000 description 2
- 239000004292 methyl p-hydroxybenzoate Substances 0.000 description 2
- LXCFILQKKLGQFO-UHFFFAOYSA-N methylparaben Chemical compound COC(=O)C1=CC=C(O)C=C1 LXCFILQKKLGQFO-UHFFFAOYSA-N 0.000 description 2
- 229960002216 methylparaben Drugs 0.000 description 2
- 229910052759 nickel Inorganic materials 0.000 description 2
- 229910017604 nitric acid Inorganic materials 0.000 description 2
- 231100001184 nonphytotoxic Toxicity 0.000 description 2
- 235000006408 oxalic acid Nutrition 0.000 description 2
- 239000000575 pesticide Substances 0.000 description 2
- 230000003032 phytopathogenic effect Effects 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- WGYKZJWCGVVSQN-UHFFFAOYSA-O propan-1-aminium Chemical compound CCC[NH3+] WGYKZJWCGVVSQN-UHFFFAOYSA-O 0.000 description 2
- 238000011160 research Methods 0.000 description 2
- 239000002689 soil Substances 0.000 description 2
- 241000894007 species Species 0.000 description 2
- 239000000758 substrate Substances 0.000 description 2
- 230000002195 synergetic effect Effects 0.000 description 2
- 239000011975 tartaric acid Substances 0.000 description 2
- 235000002906 tartaric acid Nutrition 0.000 description 2
- REEQLXCGVXDJSQ-UHFFFAOYSA-N trichlopyr Chemical compound OC(=O)COC1=NC(Cl)=C(Cl)C=C1Cl REEQLXCGVXDJSQ-UHFFFAOYSA-N 0.000 description 2
- YNJBWRMUSHSURL-UHFFFAOYSA-N trichloroacetic acid Chemical compound OC(=O)C(Cl)(Cl)Cl YNJBWRMUSHSURL-UHFFFAOYSA-N 0.000 description 2
- 239000011701 zinc Substances 0.000 description 2
- 229910052725 zinc Inorganic materials 0.000 description 2
- NIBLDNQQTIFBAI-UHFFFAOYSA-N 2-amino-4-methylphosphanylbutanoic acid Chemical compound CPCCC(N)C(O)=O NIBLDNQQTIFBAI-UHFFFAOYSA-N 0.000 description 1
- KDSNLYIMUZNERS-UHFFFAOYSA-O 2-methylpropanaminium Chemical compound CC(C)C[NH3+] KDSNLYIMUZNERS-UHFFFAOYSA-O 0.000 description 1
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 1
- JDRFUUBRGGDEIZ-UHFFFAOYSA-N 3,6-dichloro-2-methoxybenzoate;dimethylazanium Chemical compound CNC.COC1=C(Cl)C=CC(Cl)=C1C(O)=O JDRFUUBRGGDEIZ-UHFFFAOYSA-N 0.000 description 1
- 241000219240 Acer pictum subsp. mono Species 0.000 description 1
- 235000003840 Amygdalus nana Nutrition 0.000 description 1
- 244000296825 Amygdalus nana Species 0.000 description 1
- 239000005711 Benzoic acid Substances 0.000 description 1
- 101000742062 Bos taurus Protein phosphatase 1G Proteins 0.000 description 1
- 235000003801 Castanea crenata Nutrition 0.000 description 1
- 244000209117 Castanea crenata Species 0.000 description 1
- 241000723436 Chamaecyparis obtusa Species 0.000 description 1
- 241001427681 Clethra barbinervis Species 0.000 description 1
- 241000195493 Cryptophyta Species 0.000 description 1
- QXNVGIXVLWOKEQ-UHFFFAOYSA-N Disodium Chemical compound [Na][Na] QXNVGIXVLWOKEQ-UHFFFAOYSA-N 0.000 description 1
- 241000331215 Hydrangea hirta Species 0.000 description 1
- 239000005909 Kieselgur Substances 0.000 description 1
- 241000534018 Larix kaempferi Species 0.000 description 1
- 241000735234 Ligustrum Species 0.000 description 1
- 239000005573 Linuron Substances 0.000 description 1
- 241000227175 Lyonia Species 0.000 description 1
- 239000005575 MCPB Substances 0.000 description 1
- 101150039283 MCPB gene Proteins 0.000 description 1
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical group [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 description 1
- 241001411071 Neillia incisa Species 0.000 description 1
- 235000000405 Pinus densiflora Nutrition 0.000 description 1
- 240000008670 Pinus densiflora Species 0.000 description 1
- 241000209504 Poaceae Species 0.000 description 1
- 235000011432 Prunus Nutrition 0.000 description 1
- 241000219492 Quercus Species 0.000 description 1
- 241001480055 Quercus mongolica Species 0.000 description 1
- 241001092459 Rubus Species 0.000 description 1
- 244000189123 Rumex japonicus Species 0.000 description 1
- 235000005247 Rumex japonicus Nutrition 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 241000610427 Styrax japonicus Species 0.000 description 1
- 240000003583 Ternstroemia japonica Species 0.000 description 1
- 241000134415 Toxicodendron trichocarpum Species 0.000 description 1
- 235000012545 Vaccinium macrocarpon Nutrition 0.000 description 1
- 235000002118 Vaccinium oxycoccus Nutrition 0.000 description 1
- 241000673664 Viburnum dilatatum Species 0.000 description 1
- 244000131415 Zanthoxylum piperitum Species 0.000 description 1
- 235000008853 Zanthoxylum piperitum Nutrition 0.000 description 1
- 241001520823 Zoysia Species 0.000 description 1
- NFZOPFLWGIQSEA-UHFFFAOYSA-N [NH4+].CCOP([O-])(=O)OC(N)=O Chemical compound [NH4+].CCOP([O-])(=O)OC(N)=O NFZOPFLWGIQSEA-UHFFFAOYSA-N 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000004480 active ingredient Substances 0.000 description 1
- 125000003342 alkenyl group Chemical group 0.000 description 1
- 150000001346 alkyl aryl ethers Chemical class 0.000 description 1
- 239000003945 anionic surfactant Substances 0.000 description 1
- 239000003242 anti bacterial agent Substances 0.000 description 1
- 230000002660 anti-spreading effect Effects 0.000 description 1
- ZXVOCOLRQJZVBW-UHFFFAOYSA-N azane;ethanol Chemical class N.CCO ZXVOCOLRQJZVBW-UHFFFAOYSA-N 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 235000010233 benzoic acid Nutrition 0.000 description 1
- 230000003115 biocidal effect Effects 0.000 description 1
- 230000005540 biological transmission Effects 0.000 description 1
- HQABUPZFAYXKJW-UHFFFAOYSA-O butylazanium Chemical compound CCCC[NH3+] HQABUPZFAYXKJW-UHFFFAOYSA-O 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 235000021019 cranberries Nutrition 0.000 description 1
- 235000004634 cranberry Nutrition 0.000 description 1
- JQVDAXLFBXTEQA-UHFFFAOYSA-O dibutylazanium Chemical compound CCCC[NH2+]CCCC JQVDAXLFBXTEQA-UHFFFAOYSA-O 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- HPNMFZURTQLUMO-UHFFFAOYSA-O diethylammonium Chemical compound CC[NH2+]CC HPNMFZURTQLUMO-UHFFFAOYSA-O 0.000 description 1
- UAOMVDZJSHZZME-UHFFFAOYSA-N diisopropylamine Chemical compound CC(C)NC(C)C UAOMVDZJSHZZME-UHFFFAOYSA-N 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- KCIDZIIHRGYJAE-YGFYJFDDSA-L dipotassium;[(2r,3r,4s,5r,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] phosphate Chemical compound [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
- WEHWNAOGRSTTBQ-UHFFFAOYSA-O dipropylazanium Chemical compound CCC[NH2+]CCC WEHWNAOGRSTTBQ-UHFFFAOYSA-O 0.000 description 1
- 235000021186 dishes Nutrition 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 230000000855 fungicidal effect Effects 0.000 description 1
- 239000000417 fungicide Substances 0.000 description 1
- 102000005396 glutamine synthetase Human genes 0.000 description 1
- 108020002326 glutamine synthetase Proteins 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 238000003306 harvesting Methods 0.000 description 1
- PYGSKMBEVAICCR-UHFFFAOYSA-N hexa-1,5-diene Chemical group C=CCCC=C PYGSKMBEVAICCR-UHFFFAOYSA-N 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 230000000977 initiatory effect Effects 0.000 description 1
- 238000011835 investigation Methods 0.000 description 1
- JJWLVOIRVHMVIS-UHFFFAOYSA-N isopropylamine Chemical class CC(C)N JJWLVOIRVHMVIS-UHFFFAOYSA-N 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
- 230000010534 mechanism of action Effects 0.000 description 1
- JACMPVXHEARCBO-UHFFFAOYSA-N n-pentylpentan-1-amine Chemical compound CCCCCNCCCCC JACMPVXHEARCBO-UHFFFAOYSA-N 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- 210000000056 organ Anatomy 0.000 description 1
- 230000000149 penetrating effect Effects 0.000 description 1
- DPBLXKKOBLCELK-UHFFFAOYSA-O pentylazanium Chemical compound CCCCC[NH3+] DPBLXKKOBLCELK-UHFFFAOYSA-O 0.000 description 1
- 235000014774 prunus Nutrition 0.000 description 1
- UQDJGEHQDNVPGU-UHFFFAOYSA-N serine phosphoethanolamine Chemical compound [NH3+]CCOP([O-])(=O)OCC([NH3+])C([O-])=O UQDJGEHQDNVPGU-UHFFFAOYSA-N 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- DOMXUEMWDBAQBQ-WEVVVXLNSA-N terbinafine Chemical compound C1=CC=C2C(CN(C\C=C\C#CC(C)(C)C)C)=CC=CC2=C1 DOMXUEMWDBAQBQ-WEVVVXLNSA-N 0.000 description 1
- 244000082735 tidal marsh flat sedge Species 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 239000004563 wettable powder Substances 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
- C07F9/30—Phosphinic acids [R2P(=O)(OH)]; Thiophosphinic acids ; [R2P(=X1)(X2H) (X1, X2 are each independently O, S or Se)]
- C07F9/301—Acyclic saturated 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
- A01N57/20—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-carbon bonds containing acyclic or cycloaliphatic 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 (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP15742277A JPS5492627A (en) | 1977-12-28 | 1977-12-28 | Herbicidal composition |
| JP15742177A JPS5492626A (en) | 1977-12-28 | 1977-12-28 | Herbicide |
| JP15893277A JPS5492628A (en) | 1977-12-29 | 1977-12-29 | Herbicide |
| JP3605978A JPS59484B2 (ja) | 1978-03-30 | 1978-03-30 | 除草剤組成物 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE2856260A1 true DE2856260A1 (de) | 1979-07-05 |
Family
ID=27460198
Family Applications (3)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE19782856260 Ceased DE2856260A1 (de) | 1977-12-28 | 1978-12-27 | Herbicide |
| DE2857660A Expired DE2857660C2 (de) | 1977-12-28 | 1978-12-27 | Herbizide Zusammensetzung zur Kontrolle von perrennierenden Unkräutern und Büschen |
| DE2858198A Expired DE2858198C2 (enExample) | 1977-12-28 | 1978-12-27 |
Family Applications After (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE2857660A Expired DE2857660C2 (de) | 1977-12-28 | 1978-12-27 | Herbizide Zusammensetzung zur Kontrolle von perrennierenden Unkräutern und Büschen |
| DE2858198A Expired DE2858198C2 (enExample) | 1977-12-28 | 1978-12-27 |
Country Status (9)
| Country | Link |
|---|---|
| US (3) | US4265654A (enExample) |
| AU (1) | AU524653B2 (enExample) |
| BR (1) | BR7808543A (enExample) |
| CA (1) | CA1131460A (enExample) |
| DE (3) | DE2856260A1 (enExample) |
| FR (1) | FR2413034A1 (enExample) |
| GB (1) | GB2011416B (enExample) |
| IT (1) | IT1160408B (enExample) |
| MY (1) | MY8400159A (enExample) |
Cited By (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0009620A1 (de) * | 1978-09-08 | 1980-04-16 | Hoechst Aktiengesellschaft | Herbizide Mittel sowie deren Verwendung zur Unkrautbekämpfung |
| EP0076470A1 (de) * | 1981-10-01 | 1983-04-13 | Hoechst Aktiengesellschaft | Herbizide Mittel |
| EP0162326A3 (en) * | 1984-05-02 | 1986-04-16 | Hoechst Aktiengesellschaft | Herbicidal agents |
| US4923996A (en) * | 1988-02-19 | 1990-05-08 | Hoechst Aktiengesellschaft | Optically active rhodium complexes of 3,4-bis(diarylphosphino)pyrrolidines and their use for the preparation of phosphinothricin by asymmetric hydrogenation |
| EP0508296A1 (de) * | 1991-04-06 | 1992-10-14 | Hoechst Schering AgrEvo GmbH | Verfahren zur Herstellung phosphorhaltiger L-Aminosäuren, deren Derivate und Zwischenprodukte für dieses Verfahren |
| US5420329A (en) * | 1991-12-13 | 1995-05-30 | Hoechst Aktiengesellschaft | Process for the preparation of L-phosphinothricin and its derivatives |
| US5767309A (en) * | 1994-03-04 | 1998-06-16 | Hoechst Schering Agrevo Gmbh | Processes for preparing L!- or D!-homoalanin-4-yl-(methyl)phosphinic acid and salts thereof by racemate resolution |
| WO1999052367A1 (de) * | 1998-04-08 | 1999-10-21 | Aventis Cropscience Gmbh | Synergistische herbizide mittel auf basis von phosphorhaltigen blattherbiziden, imidazolinonen und wuchsstoffherbiziden |
| WO2000008936A1 (de) | 1998-08-13 | 2000-02-24 | Aventis Cropscience Gmbh | Herbizide mittel für tolerante oder resistente maiskulturen |
| WO2000008937A1 (de) | 1998-08-13 | 2000-02-24 | Aventis Cropscience Gmbh | Herbizide mittel für tolerante oder resistente baumwollkulturen |
| US6723681B2 (en) | 1998-08-13 | 2004-04-20 | Hoechst Schering Agrevo Gmbh | Herbicidal compositions for tolerant or resistant cereal crops |
| US6936444B1 (en) | 1999-04-30 | 2005-08-30 | Aventis Cropscience Gmbh | Process for the preparation of L-phosphinothricine by enzymatic transamination with aspartate |
| US7105470B1 (en) | 1998-08-13 | 2006-09-12 | Hoechst Schering Agrevo Gmbh | Herbicidal compositions for tolerant or resistant soybean crops |
| US8536094B2 (en) | 1998-08-13 | 2013-09-17 | Bayer Intellectual Property Gmbh | Herbicidal compositions for tolerant or resistant rice crops |
Families Citing this family (85)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| 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 |
| EP0010067B1 (en) * | 1978-10-05 | 1983-08-31 | Ciba-Geigy Ag | Process for influencing plant growth |
| DE3035554A1 (de) * | 1980-09-20 | 1982-05-06 | Hoechst Ag, 6000 Frankfurt | Herbizide mittel |
| US4466913A (en) * | 1981-06-30 | 1984-08-21 | Maiji Seika Kaisha Ltd. | Phosphorus-containing compounds and process for producing the same |
| DE3131495A1 (de) * | 1981-08-08 | 1983-03-03 | Hoechst Ag, 6000 Frankfurt | "herbizide mittel" |
| US5059241A (en) * | 1983-07-06 | 1991-10-22 | Union Oil Company Of California | Plant growth regulation |
| US4863506A (en) * | 1983-07-06 | 1989-09-05 | Union Oil Company Of California | Methods for regulating the growth of plants and growth regulant compositions |
| US4466823A (en) * | 1983-11-18 | 1984-08-21 | Shell Oil Company | Control of unwanted sicklepod plants |
| DE3817956A1 (de) * | 1988-05-27 | 1989-12-07 | Hoechst Ag | Verfahren zur herstellung phosphorhaltiger l-aminosaeuren sowie ihrer ester und n-derivate |
| EP0530506B1 (de) * | 1991-08-03 | 1996-05-01 | Hoechst Schering AgrEvo GmbH | Optisch aktive Omega-Halogen-2-amino-alkancarbonsäure-derivate, Verfahren zu ihrer Herstellung und ihre Verwendung zur Herstellung optisch aktiver phosphorhaltiger Alpha-Aminosäuren |
| EP0585210A1 (en) * | 1992-08-24 | 1994-03-02 | Monsanto Company | Herbicidal compositions |
| US6383985B1 (en) | 2000-01-10 | 2002-05-07 | Eco-Care Technologies, Inc. | Herbicidal fatty acid and maleic hydrazide salt compositions |
| CN102027992A (zh) * | 2010-12-21 | 2011-04-27 | 利尔化学股份有限公司 | 非耕地、果园用增效除草组合物 |
| EP3244742A1 (en) * | 2015-01-15 | 2017-11-22 | Basf Se | Herbicidal combination comprising saflufenacil and glufosinate |
| WO2017009061A1 (en) | 2015-07-10 | 2017-01-19 | BASF Agro B.V. | Herbicidal composition comprising cinmethylin and saflufenacil |
| US11219215B2 (en) | 2015-07-10 | 2022-01-11 | BASF Agro B.V. | Herbicidal composition comprising cinmethylin and specific inhibitors of protoporphyrinogen oxidase |
| US11219212B2 (en) | 2015-07-10 | 2022-01-11 | BASF Agro B.V. | Herbicidal composition comprising cinmethylin and imazamox |
| AU2016292678B2 (en) | 2015-07-10 | 2020-12-24 | BASF Agro B.V. | Method for controlling herbicide resistant or tolerant weeds |
| MY189172A (en) | 2015-07-10 | 2022-01-31 | Basf Agro Bv | Herbicidal composition comprising cinmethylin and specific quinolinecarboxylic acids |
| US10980232B2 (en) | 2015-07-10 | 2021-04-20 | BASF Agro B.V. | Herbicidal composition comprising cinmethylin and pyroxasulfone |
| US20180199568A1 (en) | 2015-07-10 | 2018-07-19 | BASF Agro B.V. | Herbicidal composition comprising cinmethylin and pethoxamid |
| KR102549057B1 (ko) | 2015-07-10 | 2023-06-29 | 바스프 아그로 비.브이. | 신메틸린 및 아세토클로르 또는 프레틸라클로르를 포함하는 제초제 조성물 |
| PL3319427T3 (pl) | 2015-07-10 | 2020-05-18 | BASF Agro B.V. | Kompozycja chwastobójcza zawierająca cynmetalinę i dimetenamid |
| PL3319435T3 (pl) | 2015-07-10 | 2020-07-27 | BASF Agro B.V. | Kompozycja chwastobójcza zawierająca cynmetalinę i chlomazon |
| CN105660687A (zh) * | 2016-03-01 | 2016-06-15 | 江苏七洲绿色化工股份有限公司 | 一种精草铵膦与麦草畏的复配组合物 |
| CN105660688A (zh) * | 2016-03-01 | 2016-06-15 | 江苏七洲绿色化工股份有限公司 | 一种精草铵膦可溶性制剂及其制备方法 |
| CN106070311A (zh) * | 2016-06-22 | 2016-11-09 | 南京华洲药业有限公司 | 一种含草铵膦与氟吡甲禾灵的除草组合物及其应用 |
| CN106070312A (zh) * | 2016-06-22 | 2016-11-09 | 南京华洲药业有限公司 | 一种含草铵膦与单嘧磺隆的除草组合物及其应用 |
| CN106070310A (zh) * | 2016-06-22 | 2016-11-09 | 南京华洲药业有限公司 | 一种含草铵膦与氟酮磺隆的除草组合物及其应用 |
| WO2018108797A1 (de) | 2016-12-15 | 2018-06-21 | Bayer Cropscience Aktiengesellschaft | Verfahren zur herstellung von l-glufosinat oder dessen salzen unter verwendung von ephedrin |
| WO2018108794A1 (de) | 2016-12-15 | 2018-06-21 | Bayer Cropscience Aktiengesellschaft | Verfahren zur herstellung von d-glufosinat oder dessen salzen unter verwendung von ephedrin |
| BR112020001585A2 (pt) | 2017-07-27 | 2020-08-11 | Basf Se | usos de uma composição e método para controlar plantas prejudiciais em uma cultura de campo tolerante a glufosinato |
| EP3440937A1 (en) | 2017-08-09 | 2019-02-13 | Basf Se | Herbicidal mixtures comprising l-glufosinate or its salt and a second herbicide |
| TW201929671A (zh) * | 2017-08-09 | 2019-08-01 | 德商巴地斯顏料化工廠 | 包含l-固殺草或其鹽及至少一種光合成抑制劑之除草混合物 |
| WO2019030102A1 (en) | 2017-08-09 | 2019-02-14 | Basf Se | HERBICIDE MIXTURES COMPRISING L-GLUFOSINATE OR A SALT THEREOF AND GLYPHOSATE OR SALTS THEREOF |
| WO2019030101A1 (en) | 2017-08-09 | 2019-02-14 | Basf Se | HERBICIDE MIXTURES COMPRISING L-GLUFOSINATE OR SALT THEREOF AND AT LEAST ONE WHITENING HERBICIDE |
| WO2019030100A1 (en) | 2017-08-09 | 2019-02-14 | Basf Se | HERBICIDE MIXTURES COMPRISING L-GLUFOSINATE OR SALT THEREOF AND AT LEAST ONE MITOSE INHIBITOR |
| CR20230111A (es) * | 2017-08-09 | 2023-03-28 | Basf Se | MEZCLAS HERBICIDAS QUE COMPRENDEN L-GLUFOSINATO O SUS SALES, Y SAFLUFENACIL (Divisional 2020-0062) |
| WO2019030090A1 (en) | 2017-08-09 | 2019-02-14 | Basf Se | HERBICIDE MIXTURES COMPRISING L-GLUFOSINATE AND THEIR USE IN RICE CROPS |
| CA3070177A1 (en) | 2017-08-09 | 2019-02-14 | Basf Se | Herbicidal mixtures comprising l-glufosinate and their use in canola cultures |
| WO2019030103A1 (en) * | 2017-08-09 | 2019-02-14 | Basf Se | HERBICIDE MIXTURES COMPRISING L-GLUFOSINATE OR SALT THEREOF AND AT LEAST ONE AUXINIC HERBICIDE |
| WO2019030097A2 (en) | 2017-08-09 | 2019-02-14 | Basf Se | HERBICIDE MIXTURES COMPRISING L-GLUFOSINATE AND THEIR USE IN SOJA CULTURES |
| WO2019030088A1 (en) | 2017-08-09 | 2019-02-14 | Basf Se | HERBICIDE MIXTURES COMPRISING L-GLUFOSINATE AND THEIR USE IN CEREAL CROPS |
| WO2019030104A1 (en) | 2017-08-09 | 2019-02-14 | Basf Se | HERBICIDE MIXTURES COMPRISING L-GLUFOSINATE OR SALT THEREOF AND AT LEAST ONE VLCFA INHIBITOR |
| MX2020001585A (es) | 2017-08-09 | 2020-09-28 | Basf Se | Mezclas herbicidas que comprenden l-glufosinato y su uso en cultivos de algodon. |
| WO2019030087A1 (en) | 2017-08-09 | 2019-02-14 | Basf Se | HERBICIDE MIXTURES COMPRISING L-GLUFOSINATE OR SALT THEREOF AND AT LEAST ONE INHIBITOR OF LIPID BIOSYNTHESIS |
| WO2019030089A1 (en) | 2017-08-09 | 2019-02-14 | Basf Se | HERBICIDE MIXTURES COMPRISING L-GLUFOSINATE OR SALT THEREOF AND AT LEAST ONE ALS INHIBITOR |
| EP3440939A1 (en) | 2017-08-09 | 2019-02-13 | Basf Se | Herbicidal mixtures comprising l-glufosinate |
| CN108174864A (zh) * | 2017-11-21 | 2018-06-19 | 南京红太阳股份有限公司 | 一种含草铵膦与氯酯磺草胺的除草组合物及其应用 |
| CN108588045B (zh) | 2018-03-09 | 2019-12-10 | 浙江大学 | 谷氨酸脱氢酶突变体及其在制备l-草铵膦中的应用 |
| CN110184246B (zh) | 2019-05-15 | 2020-10-13 | 浙江大学 | 谷氨酸脱氢酶突变体及其应用 |
| MX2022009078A (es) | 2020-01-23 | 2022-08-15 | Basf Se | Formulaciones de ppo que contienen sulfatos de eter. |
| BR112022014879A2 (pt) | 2020-01-31 | 2022-09-20 | Basf Se | Combinação de herbicidas, composição, métodos de produção de combinações de herbicidas, de tratamento ou proteção de plantas produtoras em fileiras e de tratamento ou proteção de plantas especializadas e uso da combinação de herbicidas |
| BR112022014831A2 (pt) | 2020-01-31 | 2022-09-27 | Basf Se | Combinação de herbicidas, composição, métodos para produzir uma combinação de herbicidas, para controlar o crescimento de plantas indesejadas e para tratar ou proteger culturas e uso de uma combinação de herbicidas |
| BR112022014758A2 (pt) | 2020-01-31 | 2022-10-11 | Basf Se | Combinação de herbicidas, composição, métodos para produzir uma combinação de herbicidas, para controlar o crescimento indesejado das plantas e para tratar ou proteger culturas e uso da combinação de herbicidas |
| WO2021151738A1 (en) | 2020-01-31 | 2021-08-05 | Basf Se | Herbicide combinations comprising glufosinate and epyrifenacil |
| WO2021151753A1 (en) | 2020-01-31 | 2021-08-05 | Basf Se | Herbicide combinations comprising glufosinate and selected ppo inhibitors |
| US20230076646A1 (en) | 2020-01-31 | 2023-03-09 | Basf Se | Herbicide combinations comprising glufosinate and sulfentrazone |
| BR112022014824A2 (pt) | 2020-01-31 | 2022-12-13 | Basf Se | Combinação de herbicidas, composição, métodos de produção de combinações herbicidas, de tratamento ou proteção de plantas produtoras em fileiras e de tratamento ou proteção de plantas especializadas e uso da composição herbicida |
| BR112022014950A2 (pt) | 2020-01-31 | 2022-09-20 | Basf Se | Combinação de herbicidas, composição, métodos de produção de combinações de herbicidas, de controle do crescimento vegetal indesejado e de tratamento ou proteção de plantas e uso da combinação de herbicidas |
| US20230091043A1 (en) | 2020-01-31 | 2023-03-23 | Basf Se | Herbicide Combinations Comprising Glufosinate and Carfentrazone-Ethyl |
| US20230054749A1 (en) | 2020-01-31 | 2023-02-23 | Basf Se | Herbicide Combinations Comprising Glufosinate and Flumiclorac-pentyl |
| US20230075365A1 (en) | 2020-01-31 | 2023-03-09 | Basf Se | Herbicide combinations comprising glufosinate and selected ppo inhibitors |
| US20230088774A1 (en) | 2020-01-31 | 2023-03-23 | Basf Se | Herbicide Combinations Comprising Glufosinate and Oxadiazon |
| US20230060640A1 (en) | 2020-01-31 | 2023-03-02 | Basf Se | Herbicide combinations comprising glufosinate and pyraflufen-ethyl |
| BR112022015061A2 (pt) | 2020-01-31 | 2022-09-20 | Basf Se | Combinação de herbicidas, composição, métodos para produzir uma combinação de herbicidas, para controlar o crescimento indesejado das plantas, para tratar ou proteger culturas e uso de uma combinação de herbicidas |
| US12262715B2 (en) | 2020-02-05 | 2025-04-01 | Basf Se | Herbicidal mixtures comprising L-glufosinate or its salt and at least one protoporphyrinogen-IX oxidase inhibitor |
| BR112022026180A2 (pt) * | 2020-06-29 | 2023-01-17 | Monsanto Technology Llc | Misturas de herbicida auxínico e l-glufosinato |
| EP4000400A1 (en) | 2020-11-17 | 2022-05-25 | Basf Se | Herbicide combination comprising glufosinate, saflufenacil and trifludimoxazin |
| US20240023556A1 (en) | 2020-10-12 | 2024-01-25 | Basf Se | Herbicide combination comprising glufosinate, saflufenacil and trifludimoxazin |
| KR20230097101A (ko) | 2020-10-27 | 2023-06-30 | 바스프 에스이 | 살충제 마이크로에멀젼 조성물 |
| CA3207197A1 (en) | 2021-02-05 | 2022-08-11 | Murat Mertoglu | Liquid herbicidal compositions |
| IL307248A (en) | 2021-04-01 | 2023-11-01 | Basf Se | Methods for preparing L-glufosinate |
| CA3219689A1 (en) | 2021-05-21 | 2022-11-24 | Anna SOYK | Computer-implemented method for applying a glutamine synthetase inhibitor on an agricultural field |
| AU2022385443A1 (en) | 2021-11-15 | 2024-05-23 | Basf Se | Method for increasing the efficacy of a herbicide |
| CN119451575A (zh) | 2022-06-29 | 2025-02-14 | 巴斯夫欧洲公司 | 包含l-草铵膦或其盐和第二除草剂的除草混合物 |
| CN119894374A (zh) | 2022-09-14 | 2025-04-25 | 巴斯夫欧洲公司 | 烷基醚硫酸盐用于改善除草剂的功效的用途 |
| EP4338592A1 (en) | 2022-09-15 | 2024-03-20 | Basf Se | Use of compound for improving the efficacy of herbicides |
| AR131675A1 (es) * | 2023-01-24 | 2025-04-23 | Upl Mauritius Ltd | Una combinación herbicida, una composición y método de control de malas hierbas utilizando las mismas |
| WO2024160739A1 (en) * | 2023-01-30 | 2024-08-08 | Upl Mauritius Limited | An herbicidal combination, composition and method of controlling weeds using the same |
| WO2024165545A1 (en) * | 2023-02-07 | 2024-08-15 | Upl Mauritius Limited | An herbicidal combination, composition and method of controlling weeds using the same |
| AU2024216911A1 (en) * | 2023-02-07 | 2025-08-21 | Upl Europe Supply Chain Gmbh | An herbicidal combination, composition and method of controlling weeds using the same |
| AR133862A1 (es) | 2023-09-21 | 2025-11-12 | Specialty Operations France | Emulsión en agua concentrada que comprende glufosinato, inhibidor de vlcfa y tensioactivos específicos |
| AR133857A1 (es) | 2023-09-21 | 2025-11-05 | Specialty Operations France | Composiciones herbicidas que comprenden tensioactivos específicos |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DD116236A1 (enExample) | 1974-11-08 | 1975-11-12 | ||
| DE2717440A1 (de) | 1976-05-17 | 1977-12-01 | Hoechst Ag | Herbizide mittel |
-
1978
- 1978-12-20 GB GB7849385A patent/GB2011416B/en not_active Expired
- 1978-12-20 US US05/971,636 patent/US4265654A/en not_active Expired - Lifetime
- 1978-12-22 AU AU42864/78A patent/AU524653B2/en not_active Expired
- 1978-12-27 DE DE19782856260 patent/DE2856260A1/de not_active Ceased
- 1978-12-27 DE DE2857660A patent/DE2857660C2/de not_active Expired
- 1978-12-27 CA CA318,635A patent/CA1131460A/en not_active Expired
- 1978-12-27 DE DE2858198A patent/DE2858198C2/de not_active Expired
- 1978-12-27 IT IT31342/78A patent/IT1160408B/it active
- 1978-12-27 BR BR7808543A patent/BR7808543A/pt unknown
- 1978-12-28 FR FR7836784A patent/FR2413034A1/fr active Granted
-
1979
- 1979-08-20 US US06/068,185 patent/US4382812A/en not_active Expired - Lifetime
-
1982
- 1982-09-21 US US06/420,929 patent/US4552583A/en not_active Expired - Lifetime
-
1984
- 1984-12-30 MY MY159/84A patent/MY8400159A/xx unknown
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DD116236A1 (enExample) | 1974-11-08 | 1975-11-12 | ||
| DE2717440A1 (de) | 1976-05-17 | 1977-12-01 | Hoechst Ag | Herbizide mittel |
Non-Patent Citations (3)
| Title |
|---|
| japanische Offenlegungsschrift 49-24644 |
| japanische Offenlegungsschrift 49-55835 |
| japanische Patentveröffentlichungen 48-85538 und 49-31890 |
Cited By (31)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0009620A1 (de) * | 1978-09-08 | 1980-04-16 | Hoechst Aktiengesellschaft | Herbizide Mittel sowie deren Verwendung zur Unkrautbekämpfung |
| EP0076470A1 (de) * | 1981-10-01 | 1983-04-13 | Hoechst Aktiengesellschaft | Herbizide Mittel |
| EP0162326A3 (en) * | 1984-05-02 | 1986-04-16 | Hoechst Aktiengesellschaft | Herbicidal agents |
| US4923996A (en) * | 1988-02-19 | 1990-05-08 | Hoechst Aktiengesellschaft | Optically active rhodium complexes of 3,4-bis(diarylphosphino)pyrrolidines and their use for the preparation of phosphinothricin by asymmetric hydrogenation |
| EP0508296A1 (de) * | 1991-04-06 | 1992-10-14 | Hoechst Schering AgrEvo GmbH | Verfahren zur Herstellung phosphorhaltiger L-Aminosäuren, deren Derivate und Zwischenprodukte für dieses Verfahren |
| AU646938B2 (en) * | 1991-04-06 | 1994-03-10 | Hoechst Aktiengesellschaft | Process for the preparation of phosphorus-containing L-amino acids, their derivatives and intermediates for this process |
| US5442088A (en) * | 1991-04-06 | 1995-08-15 | Hoechst Aktiengesellschaft | Process for the preparation of phosphorus-containing L-amino acids, their derivatives and intermediates for this process |
| US5420329A (en) * | 1991-12-13 | 1995-05-30 | Hoechst Aktiengesellschaft | Process for the preparation of L-phosphinothricin and its derivatives |
| US5767309A (en) * | 1994-03-04 | 1998-06-16 | Hoechst Schering Agrevo Gmbh | Processes for preparing L!- or D!-homoalanin-4-yl-(methyl)phosphinic acid and salts thereof by racemate resolution |
| US5869668A (en) * | 1994-03-04 | 1999-02-09 | Hoechst Schering Agrevo Gmbh | Processes for preparing L!- or D!-homoalanin-4-yl-(methyl) phosphinic acid and salts thereof by racemate resolution |
| US6436874B1 (en) | 1998-04-08 | 2002-08-20 | Aventis Cropscience Gmbh | Synergistic herbicidal agents based on leaf herbicides containing phosphorus, imidazolinones and hormone weed killers |
| WO1999052367A1 (de) * | 1998-04-08 | 1999-10-21 | Aventis Cropscience Gmbh | Synergistische herbizide mittel auf basis von phosphorhaltigen blattherbiziden, imidazolinonen und wuchsstoffherbiziden |
| US6723681B2 (en) | 1998-08-13 | 2004-04-20 | Hoechst Schering Agrevo Gmbh | Herbicidal compositions for tolerant or resistant cereal crops |
| EP2319317A1 (de) | 1998-08-13 | 2011-05-11 | Bayer CropScience AG | Herbizide Mittel für tolerante oder resistente Baumwollkulturen |
| WO2000008936A1 (de) | 1998-08-13 | 2000-02-24 | Aventis Cropscience Gmbh | Herbizide mittel für tolerante oder resistente maiskulturen |
| EP1104992B1 (de) * | 1998-08-13 | 2005-03-09 | Bayer CropScience GmbH | Herbizide mittel für tolerante oder resistente getreidekulturen |
| EP2904902A1 (de) | 1998-08-13 | 2015-08-12 | Bayer CropScience AG | Herbizide Mittel für tolerante oder resistente Sojakulturen |
| US7012040B2 (en) | 1998-08-13 | 2006-03-14 | Hoechst Schering Agrevo Gmbh | Herbicidal compositions for tolerant or resistant maize crops |
| US7105470B1 (en) | 1998-08-13 | 2006-09-12 | Hoechst Schering Agrevo Gmbh | Herbicidal compositions for tolerant or resistant soybean crops |
| BG65288B1 (bg) * | 1998-08-13 | 2007-12-28 | Aventis Cropscience Gmbh | Хербицидни средства за толерантни или устойчиви царевични култури |
| EP2319315A1 (de) | 1998-08-13 | 2011-05-11 | Bayer CropScience AG | Herbizide Mittel für tolerante oder resistente Maiskulturen |
| WO2000008937A1 (de) | 1998-08-13 | 2000-02-24 | Aventis Cropscience Gmbh | Herbizide mittel für tolerante oder resistente baumwollkulturen |
| EP2319316A1 (de) * | 1998-08-13 | 2011-05-11 | Bayer CropScience AG | Herbizide Mittel für tolerante oder resistente Maiskulturen |
| EP2327305A1 (de) | 1998-08-13 | 2011-06-01 | Bayer CropScience AG | Herbizide Mittel für tolerante oder resistente Sojakulturen |
| EP2329719A1 (de) | 1998-08-13 | 2011-06-08 | Bayer CropScience AG | Herbizide Mittel für tolerante oder resistente Sojakulturen |
| EP2329718A1 (de) | 1998-08-13 | 2011-06-08 | Bayer CropScience AG | Herbizide Mittel für tolerante oder resistente Sojakulturen |
| US8338332B1 (en) | 1998-08-13 | 2012-12-25 | Bayer Intellectual Property Gmbh | Herbicidal composition for tolerant or resistant cotton crops |
| EP1104243B1 (de) * | 1998-08-13 | 2013-03-20 | Bayer CropScience AG | Herbizide mittel für tolerante oder resistente maiskulturen |
| US8536094B2 (en) | 1998-08-13 | 2013-09-17 | Bayer Intellectual Property Gmbh | Herbicidal compositions for tolerant or resistant rice crops |
| US8614166B2 (en) | 1998-08-13 | 2013-12-24 | Bayer Intellectual Property Gmbh | Herbicidal composition for tolerant or resistant cotton crops |
| US6936444B1 (en) | 1999-04-30 | 2005-08-30 | Aventis Cropscience Gmbh | Process for the preparation of L-phosphinothricine by enzymatic transamination with aspartate |
Also Published As
| Publication number | Publication date |
|---|---|
| US4552583A (en) | 1985-11-12 |
| US4382812A (en) | 1983-05-10 |
| BR7808543A (pt) | 1979-08-28 |
| AU524653B2 (en) | 1982-09-30 |
| DE2857660C2 (de) | 1986-08-28 |
| IT7831342A0 (it) | 1978-12-27 |
| MY8400159A (en) | 1984-12-31 |
| FR2413034B1 (enExample) | 1984-12-14 |
| US4265654A (en) | 1981-05-05 |
| GB2011416B (en) | 1982-10-20 |
| AU4286478A (en) | 1979-07-05 |
| DE2858198C2 (enExample) | 1988-02-25 |
| GB2011416A (en) | 1979-07-11 |
| CA1131460A (en) | 1982-09-14 |
| IT1160408B (it) | 1987-03-11 |
| FR2413034A1 (fr) | 1979-07-27 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE2857660C2 (de) | Herbizide Zusammensetzung zur Kontrolle von perrennierenden Unkräutern und Büschen | |
| DE2857693C2 (de) | Verfahren zur selektiven Bekämpfung bzw. Vernichtung von unerwünschtem Pflanzenwuchs in Nutzpflanzenkulturen | |
| DE2211489A1 (de) | Steuerung des Pflanzenwuchses mit N-Phosphonmethylglycin und dessen Derivate | |
| DE2915085C2 (de) | Neue herbizid wirkende Verbindungen, Verfahren zu deren Herstellung und herbizide Mittel, welche diese enthalten | |
| JPS5839127B2 (ja) | 除草剤組成物 | |
| DD210596A5 (de) | Mittel gegen nematoden und bodeninsekten und verfahren zu deren bekaempfung | |
| EP1298998B1 (de) | Präparat mit fungizider wirkung | |
| DD159523A5 (de) | Herbizide zusammensetzung | |
| DE69914885T2 (de) | Herbizide zusammensetzung | |
| DE4116626A1 (de) | Herbizide mittel | |
| JPS59484B2 (ja) | 除草剤組成物 | |
| WO2000053018A1 (en) | Herbicidal composition | |
| JPS6328041B2 (enExample) | ||
| KR830001940B1 (ko) | 제초제 조성물 | |
| DE898308C (de) | Mittel und Verfahren zur Behandlung von Pflanzen | |
| DE2258528C3 (de) | Bekämpfung von Bodeninsekten mit einem Dithiophosphorsäureester-Derivat | |
| DE2810527A1 (de) | Verfahren zur selektiven wachstumsregelung von hohem wiesenschwingel (festuca arundinacea) | |
| KR840000708B1 (ko) | 2-아미노-4-메틸-포스피노일 낙산콜린의 제조법 | |
| GB2087722A (en) | Herbicidal compositions containing 2 - amino - 4 - [(hydroxy) (methyl) phosphinoyl] butyric acid and derivatives thereof | |
| JPS6149283B2 (enExample) | ||
| AT227022B (de) | Verfahren und Mittel zum Verhindern oder Hemmen der Keimung von Pflanzensamen | |
| JPS61229804A (ja) | 非選択性除草剤 | |
| DE2926176A1 (de) | Verfahren zum oxidativen abbau von toxischen pestizide rueckstaenden | |
| JPS60172905A (ja) | 除草剤組成物 | |
| DE2856878A1 (de) | Verbesserungen im zusammenhang mit insektiziden |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| OAP | Request for examination filed | ||
| OD | Request for examination | ||
| OI | Miscellaneous see part 1 | ||
| OI | Miscellaneous see part 1 | ||
| 8131 | Rejection | ||
| AH | Division in |
Ref country code: DE Ref document number: 2857660 Format of ref document f/p: P |