CA2926878C - Composition comprising a pesticide and amide - Google Patents
Composition comprising a pesticide and amide Download PDFInfo
- Publication number
- CA2926878C CA2926878C CA2926878A CA2926878A CA2926878C CA 2926878 C CA2926878 C CA 2926878C CA 2926878 A CA2926878 A CA 2926878A CA 2926878 A CA2926878 A CA 2926878A CA 2926878 C CA2926878 C CA 2926878C
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- plants
- weight
- pesticide
- composition
- alkyl
- Prior art date
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- 239000000203 mixture Substances 0.000 title claims abstract description 82
- 239000000575 pesticide Substances 0.000 title claims abstract description 73
- 150000001408 amides Chemical class 0.000 title description 9
- -1 carboxylicacid amide Chemical class 0.000 claims abstract description 49
- 239000002904 solvent Substances 0.000 claims abstract description 30
- 238000000034 method Methods 0.000 claims abstract description 19
- 241000607479 Yersinia pestis Species 0.000 claims abstract description 12
- 230000008635 plant growth Effects 0.000 claims abstract description 10
- 244000038559 crop plants Species 0.000 claims abstract description 8
- 241000238631 Hexapoda Species 0.000 claims abstract description 7
- 241000233866 Fungi Species 0.000 claims abstract description 6
- 230000001276 controlling effect Effects 0.000 claims abstract description 6
- 230000001105 regulatory effect Effects 0.000 claims abstract description 6
- 239000002689 soil Substances 0.000 claims abstract description 6
- 201000002266 mite infestation Diseases 0.000 claims abstract description 5
- 230000003032 phytopathogenic effect Effects 0.000 claims abstract description 5
- 239000013543 active substance Substances 0.000 claims description 41
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 26
- 239000000417 fungicide Substances 0.000 claims description 18
- XAROAZKXMDRYAF-UHFFFAOYSA-N n,n-dibutylpropanamide Chemical compound CCCCN(C(=O)CC)CCCC XAROAZKXMDRYAF-UHFFFAOYSA-N 0.000 claims description 16
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 15
- 239000004009 herbicide Substances 0.000 claims description 14
- 238000002156 mixing Methods 0.000 claims description 14
- 150000007980 azole derivatives Chemical class 0.000 claims description 10
- 239000002917 insecticide Substances 0.000 claims description 10
- 125000001309 chloro group Chemical group Cl* 0.000 claims description 9
- KXDHJXZQYSOELW-UHFFFAOYSA-M Carbamate Chemical compound NC([O-])=O KXDHJXZQYSOELW-UHFFFAOYSA-M 0.000 claims description 6
- 239000005493 Chloridazon (aka pyrazone) Substances 0.000 claims description 6
- WYKYKTKDBLFHCY-UHFFFAOYSA-N chloridazon Chemical compound O=C1C(Cl)=C(N)C=NN1C1=CC=CC=C1 WYKYKTKDBLFHCY-UHFFFAOYSA-N 0.000 claims description 6
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 6
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 6
- ODNZLRLWXRXPOH-UHFFFAOYSA-N 5-amino-4-bromo-2-phenylpyridazin-3-one Chemical compound O=C1C(Br)=C(N)C=NN1C1=CC=CC=C1 ODNZLRLWXRXPOH-UHFFFAOYSA-N 0.000 claims description 5
- 125000001255 4-fluorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1F 0.000 claims description 4
- GNVMUORYQLCPJZ-UHFFFAOYSA-M Thiocarbamate Chemical compound NC([S-])=O GNVMUORYQLCPJZ-UHFFFAOYSA-M 0.000 claims description 4
- 238000004519 manufacturing process Methods 0.000 claims description 4
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 4
- 125000004201 2,4-dichlorophenyl group Chemical group [H]C1=C([H])C(*)=C(Cl)C([H])=C1Cl 0.000 claims description 3
- 125000006282 2-chlorobenzyl group Chemical group [H]C1=C([H])C(Cl)=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 3
- 125000004198 2-fluorophenyl group Chemical group [H]C1=C([H])C(F)=C(*)C([H])=C1[H] 0.000 claims description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 3
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 3
- 229910052739 hydrogen Inorganic materials 0.000 claims description 3
- 239000001257 hydrogen Substances 0.000 claims description 3
- 125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 claims description 3
- 150000001732 carboxylic acid derivatives Chemical class 0.000 abstract description 51
- 231100000674 Phytotoxicity Toxicity 0.000 abstract description 30
- 241000196324 Embryophyta Species 0.000 description 62
- 239000003053 toxin Substances 0.000 description 23
- 231100000765 toxin Toxicity 0.000 description 23
- 108700012359 toxins Proteins 0.000 description 23
- 108090000623 proteins and genes Proteins 0.000 description 18
- 125000000217 alkyl group Chemical group 0.000 description 15
- 102000004169 proteins and genes Human genes 0.000 description 15
- 239000003112 inhibitor Substances 0.000 description 14
- 235000018102 proteins Nutrition 0.000 description 12
- 240000008042 Zea mays Species 0.000 description 11
- 235000016383 Zea mays subsp huehuetenangensis Nutrition 0.000 description 11
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 11
- 235000009973 maize Nutrition 0.000 description 11
- 238000009472 formulation Methods 0.000 description 10
- 239000003921 oil Substances 0.000 description 10
- 239000000047 product Substances 0.000 description 10
- 239000002671 adjuvant Substances 0.000 description 8
- 238000010790 dilution Methods 0.000 description 8
- 239000012895 dilution Substances 0.000 description 8
- 229920000742 Cotton Polymers 0.000 description 7
- 244000299507 Gossypium hirsutum Species 0.000 description 7
- JUJWROOIHBZHMG-UHFFFAOYSA-N pyridine Substances C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 7
- 239000007921 spray Substances 0.000 description 7
- 230000015572 biosynthetic process Effects 0.000 description 6
- 239000002270 dispersing agent Substances 0.000 description 6
- 150000003839 salts Chemical class 0.000 description 6
- 240000002791 Brassica napus Species 0.000 description 5
- 235000006008 Brassica napus var napus Nutrition 0.000 description 5
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 5
- 239000005562 Glyphosate Substances 0.000 description 5
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 5
- 239000003905 agrochemical Substances 0.000 description 5
- 239000000969 carrier Substances 0.000 description 5
- 230000006378 damage Effects 0.000 description 5
- 235000014113 dietary fatty acids Nutrition 0.000 description 5
- 239000000839 emulsion Substances 0.000 description 5
- 239000000194 fatty acid Substances 0.000 description 5
- 229930195729 fatty acid Natural products 0.000 description 5
- 125000003187 heptyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 5
- 239000000243 solution Substances 0.000 description 5
- 239000000725 suspension Substances 0.000 description 5
- 239000002562 thickening agent Substances 0.000 description 5
- PXMNMQRDXWABCY-UHFFFAOYSA-N 1-(4-chlorophenyl)-4,4-dimethyl-3-(1H-1,2,4-triazol-1-ylmethyl)pentan-3-ol Chemical compound C1=NC=NN1CC(O)(C(C)(C)C)CCC1=CC=C(Cl)C=C1 PXMNMQRDXWABCY-UHFFFAOYSA-N 0.000 description 4
- IAJOBQBIJHVGMQ-UHFFFAOYSA-N 2-amino-4-[hydroxy(methyl)phosphoryl]butanoic acid Chemical compound CP(O)(=O)CCC(N)C(O)=O IAJOBQBIJHVGMQ-UHFFFAOYSA-N 0.000 description 4
- 235000009854 Cucurbita moschata Nutrition 0.000 description 4
- 239000005561 Glufosinate Substances 0.000 description 4
- 235000010469 Glycine max Nutrition 0.000 description 4
- 244000068988 Glycine max Species 0.000 description 4
- 240000005979 Hordeum vulgare Species 0.000 description 4
- 235000007340 Hordeum vulgare Nutrition 0.000 description 4
- 239000005869 Pyraclostrobin Substances 0.000 description 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
- 235000002595 Solanum tuberosum Nutrition 0.000 description 4
- 244000061456 Solanum tuberosum Species 0.000 description 4
- 239000005839 Tebuconazole Substances 0.000 description 4
- 230000000844 anti-bacterial effect Effects 0.000 description 4
- 239000003899 bactericide agent Substances 0.000 description 4
- 239000013078 crystal Substances 0.000 description 4
- JQVDAXLFBXTEQA-UHFFFAOYSA-N dibutylamine Chemical compound CCCCNCCCC JQVDAXLFBXTEQA-UHFFFAOYSA-N 0.000 description 4
- 235000013399 edible fruits Nutrition 0.000 description 4
- 239000004495 emulsifiable concentrate Substances 0.000 description 4
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 4
- 238000011156 evaluation Methods 0.000 description 4
- 150000004665 fatty acids Chemical class 0.000 description 4
- 229940097068 glyphosate Drugs 0.000 description 4
- XDDAORKBJWWYJS-UHFFFAOYSA-N glyphosate Chemical compound OC(=O)CNCP(O)(O)=O XDDAORKBJWWYJS-UHFFFAOYSA-N 0.000 description 4
- 239000008187 granular material Substances 0.000 description 4
- 230000000749 insecticidal effect Effects 0.000 description 4
- 235000012054 meals Nutrition 0.000 description 4
- YKOQQFDCCBKROY-UHFFFAOYSA-N n,n-diethylpropanamide Chemical compound CCN(CC)C(=O)CC YKOQQFDCCBKROY-UHFFFAOYSA-N 0.000 description 4
- 239000003960 organic solvent Substances 0.000 description 4
- 230000000885 phytotoxic effect Effects 0.000 description 4
- XIPFMBOWZXULIA-UHFFFAOYSA-N pivalamide Chemical compound CC(C)(C)C(N)=O XIPFMBOWZXULIA-UHFFFAOYSA-N 0.000 description 4
- 230000008654 plant damage Effects 0.000 description 4
- 238000002360 preparation method Methods 0.000 description 4
- HZRSNVGNWUDEFX-UHFFFAOYSA-N pyraclostrobin Chemical compound COC(=O)N(OC)C1=CC=CC=C1COC1=NN(C=2C=CC(Cl)=CC=2)C=C1 HZRSNVGNWUDEFX-UHFFFAOYSA-N 0.000 description 4
- 238000010188 recombinant method Methods 0.000 description 4
- 239000007787 solid Substances 0.000 description 4
- 235000013311 vegetables Nutrition 0.000 description 4
- HIXDQWDOVZUNNA-UHFFFAOYSA-N 2-(3,4-dimethoxyphenyl)-5-hydroxy-7-methoxychromen-4-one Chemical compound C=1C(OC)=CC(O)=C(C(C=2)=O)C=1OC=2C1=CC=C(OC)C(OC)=C1 HIXDQWDOVZUNNA-UHFFFAOYSA-N 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 3
- 108010000700 Acetolactate synthase Proteins 0.000 description 3
- WVDDGKGOMKODPV-UHFFFAOYSA-N Benzyl alcohol Chemical compound OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 description 3
- 235000016068 Berberis vulgaris Nutrition 0.000 description 3
- 241000335053 Beta vulgaris Species 0.000 description 3
- 239000005788 Fluxapyroxad Substances 0.000 description 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- NWBJYWHLCVSVIJ-UHFFFAOYSA-N N-benzyladenine Chemical compound N=1C=NC=2NC=NC=2C=1NCC1=CC=CC=C1 NWBJYWHLCVSVIJ-UHFFFAOYSA-N 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- 108090000829 Ribosome Inactivating Proteins Proteins 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 description 3
- 150000001298 alcohols Chemical class 0.000 description 3
- 230000001580 bacterial effect Effects 0.000 description 3
- 239000003139 biocide Substances 0.000 description 3
- 235000013877 carbamide Nutrition 0.000 description 3
- 239000004359 castor oil Substances 0.000 description 3
- 235000019438 castor oil Nutrition 0.000 description 3
- 235000013339 cereals Nutrition 0.000 description 3
- 239000006185 dispersion Substances 0.000 description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 3
- NYPJDWWKZLNGGM-UHFFFAOYSA-N fenvalerate Aalpha Natural products C=1C=C(Cl)C=CC=1C(C(C)C)C(=O)OC(C#N)C(C=1)=CC=CC=1OC1=CC=CC=C1 NYPJDWWKZLNGGM-UHFFFAOYSA-N 0.000 description 3
- SXSGXWCSHSVPGB-UHFFFAOYSA-N fluxapyroxad Chemical compound FC(F)C1=NN(C)C=C1C(=O)NC1=CC=CC=C1C1=CC(F)=C(F)C(F)=C1 SXSGXWCSHSVPGB-UHFFFAOYSA-N 0.000 description 3
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 3
- 239000003630 growth substance Substances 0.000 description 3
- RONFGUROBZGJKP-UHFFFAOYSA-N iminoctadine Chemical compound NC(N)=NCCCCCCCCNCCCCCCCCN=C(N)N RONFGUROBZGJKP-UHFFFAOYSA-N 0.000 description 3
- IRACWGPKDYUZEC-UHFFFAOYSA-N n,n-dibutyloctanamide Chemical compound CCCCCCCC(=O)N(CCCC)CCCC IRACWGPKDYUZEC-UHFFFAOYSA-N 0.000 description 3
- 229920000151 polyglycol Polymers 0.000 description 3
- 239000010695 polyglycol Substances 0.000 description 3
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 3
- JLIDBLDQVAYHNE-YKALOCIXSA-N (+)-Abscisic acid Chemical compound OC(=O)/C=C(/C)\C=C\[C@@]1(O)C(C)=CC(=O)CC1(C)C JLIDBLDQVAYHNE-YKALOCIXSA-N 0.000 description 2
- YNWVFADWVLCOPU-MDWZMJQESA-N (1E)-1-(4-chlorophenyl)-4,4-dimethyl-2-(1H-1,2,4-triazol-1-yl)pent-1-en-3-ol Chemical compound C1=NC=NN1/C(C(O)C(C)(C)C)=C/C1=CC=C(Cl)C=C1 YNWVFADWVLCOPU-MDWZMJQESA-N 0.000 description 2
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- PZBPKYOVPCNPJY-UHFFFAOYSA-N 1-[2-(allyloxy)-2-(2,4-dichlorophenyl)ethyl]imidazole Chemical compound ClC1=CC(Cl)=CC=C1C(OCC=C)CN1C=NC=C1 PZBPKYOVPCNPJY-UHFFFAOYSA-N 0.000 description 2
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- FBOUIAKEJMZPQG-BLXFFLACSA-N diniconazole-M Chemical compound C1=NC=NN1/C([C@H](O)C(C)(C)C)=C/C1=CC=C(Cl)C=C1Cl FBOUIAKEJMZPQG-BLXFFLACSA-N 0.000 description 2
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- RROQIUMZODEXOR-UHFFFAOYSA-N triforine Chemical compound O=CNC(C(Cl)(Cl)Cl)N1CCN(C(NC=O)C(Cl)(Cl)Cl)CC1 RROQIUMZODEXOR-UHFFFAOYSA-N 0.000 description 1
- RVKCCVTVZORVGD-UHFFFAOYSA-N trinexapac-ethyl Chemical group O=C1CC(C(=O)OCC)CC(=O)C1=C(O)C1CC1 RVKCCVTVZORVGD-UHFFFAOYSA-N 0.000 description 1
- KVEQCVKVIFQSGC-UHFFFAOYSA-N tritosulfuron Chemical compound FC(F)(F)C1=NC(OC)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2)C(F)(F)F)=N1 KVEQCVKVIFQSGC-UHFFFAOYSA-N 0.000 description 1
- 239000002753 trypsin inhibitor Substances 0.000 description 1
- 150000003672 ureas Chemical class 0.000 description 1
- 238000005292 vacuum distillation Methods 0.000 description 1
- JARYYMUOCXVXNK-CSLFJTBJSA-N validamycin A Chemical compound N([C@H]1C[C@@H]([C@H]([C@H](O)[C@H]1O)O[C@H]1[C@@H]([C@@H](O)[C@H](O)[C@@H](CO)O1)O)CO)[C@H]1C=C(CO)[C@@H](O)[C@H](O)[C@H]1O JARYYMUOCXVXNK-CSLFJTBJSA-N 0.000 description 1
- DBXFMOWZRXXBRN-LWKPJOBUSA-N valifenalate Chemical compound CC(C)OC(=O)N[C@@H](C(C)C)C(=O)NC(CC(=O)OC)C1=CC=C(Cl)C=C1 DBXFMOWZRXXBRN-LWKPJOBUSA-N 0.000 description 1
- 238000011514 vinification Methods 0.000 description 1
- 230000003612 virological effect Effects 0.000 description 1
- 239000003021 water soluble solvent Substances 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 241000228158 x Triticosecale Species 0.000 description 1
- 239000000230 xanthan gum Substances 0.000 description 1
- 229920001285 xanthan gum Polymers 0.000 description 1
- 235000010493 xanthan gum Nutrition 0.000 description 1
- 229940082509 xanthan gum Drugs 0.000 description 1
- 239000005943 zeta-Cypermethrin Substances 0.000 description 1
- DUBNHZYBDBBJHD-UHFFFAOYSA-L ziram Chemical compound [Zn+2].CN(C)C([S-])=S.CN(C)C([S-])=S DUBNHZYBDBBJHD-UHFFFAOYSA-L 0.000 description 1
- FJBGIXKIXPUXBY-UHFFFAOYSA-N {2-[3-(4-chlorophenyl)propyl]-2,4,4-trimethyl-1,3-oxazolidin-3-yl}(imidazol-1-yl)methanone Chemical compound C1=CN=CN1C(=O)N1C(C)(C)COC1(C)CCCC1=CC=C(Cl)C=C1 FJBGIXKIXPUXBY-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- 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
- A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
- A01N25/02—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests containing liquids as carriers, diluents or solvents
Landscapes
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Health & Medical Sciences (AREA)
- Toxicology (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Agronomy & Crop Science (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP13191608 | 2013-11-05 | ||
| EP13191608.2 | 2013-11-05 | ||
| PCT/EP2014/073368 WO2015067524A1 (en) | 2013-11-05 | 2014-10-30 | Composition comprising a pesticide and amide |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CA2926878A1 CA2926878A1 (en) | 2015-05-14 |
| CA2926878C true CA2926878C (en) | 2022-09-27 |
Family
ID=49517399
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA2926878A Active CA2926878C (en) | 2013-11-05 | 2014-10-30 | Composition comprising a pesticide and amide |
Country Status (9)
| Country | Link |
|---|---|
| US (1) | US20170295779A9 (enExample) |
| EP (1) | EP3065544A1 (enExample) |
| JP (1) | JP6462706B2 (enExample) |
| CN (1) | CN105682459A (enExample) |
| BR (1) | BR112016009977B1 (enExample) |
| CA (1) | CA2926878C (enExample) |
| IL (1) | IL245041A0 (enExample) |
| RU (1) | RU2665099C2 (enExample) |
| WO (1) | WO2015067524A1 (enExample) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN111246737B (zh) * | 2017-11-03 | 2023-07-25 | 陶氏环球技术有限责任公司 | 用于农业应用的溶剂和农药调配物 |
| WO2025012401A1 (en) * | 2023-07-13 | 2025-01-16 | Specialty Operations France | Bio-based beta-ether propionamide compounds as solvents |
| CN117441721B (zh) * | 2023-12-21 | 2024-10-08 | 山东科赛基农生物工程有限公司 | 一种包含调环酸钙和甲哌鎓的悬浮剂以及应用 |
Family Cites Families (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3027959A1 (de) * | 1980-07-24 | 1982-03-04 | Basf Ag, 6700 Ludwigshafen | Fluessige herbizidmischung |
| US4902676A (en) * | 1986-09-29 | 1990-02-20 | Nelson Research & Development Co. | Compositions comprising N,N-dialkylalkanamides |
| DE4341986A1 (de) * | 1993-12-09 | 1995-06-14 | Bayer Ag | Verwendung von Carbonsäure-amiden als Kristallisationsinhibitoren |
| DE10343390A1 (de) * | 2003-09-19 | 2005-04-14 | Bayer Cropscience Gmbh | Tensid/Lösungsmittelgemische |
| DE102004020840A1 (de) * | 2004-04-27 | 2005-11-24 | Bayer Cropscience Ag | Verwendung von Alkylcarbonsäureamiden als Penetrationsförderer |
| AU2005293899A1 (en) * | 2004-10-12 | 2006-04-20 | Bayer Cropscience Ag | Surfactant/solvent mixtures |
| EP2031966B1 (en) * | 2006-05-26 | 2018-08-22 | Huntsman Petrochemical LLC | Low odor, low volatility solvent for agricultural chemicals |
| CN101069501A (zh) * | 2007-05-28 | 2007-11-14 | 江苏龙灯化学有限公司 | 双取代长链烷基酰胺类作为结晶抑制剂在唑类农药液剂中的应用 |
| KR20100134075A (ko) * | 2008-04-30 | 2010-12-22 | 베일런트 유.에스.에이. 코포레이션 | 신규한 피리프록시펜 조성물 |
| EP2147599A1 (en) * | 2008-07-23 | 2010-01-27 | Cognis IP Management GmbH | Agricultural compositions |
| BRPI0900019A2 (pt) * | 2009-01-12 | 2010-10-19 | Rotam Agrochem Int Co Ltd | suspoemulsões com base aquosa, processo de preparação e uso desta e método de tratamento de pragas indesejadas em um local |
| US20130003774A1 (en) * | 2011-06-29 | 2013-01-03 | Robert Neil Campbell | CO2 laser |
| US9173398B2 (en) * | 2011-07-05 | 2015-11-03 | Cognis Ip Management Gmbh | Biocide compositions |
| CA2844643C (en) * | 2011-08-11 | 2019-09-24 | Bayer Intellectual Property Gmbh | Use and agrochemical composition of carboxylic acid dibutylamides |
-
2014
- 2014-10-30 US US15/031,656 patent/US20170295779A9/en not_active Abandoned
- 2014-10-30 RU RU2016121720A patent/RU2665099C2/ru not_active IP Right Cessation
- 2014-10-30 BR BR112016009977A patent/BR112016009977B1/pt active IP Right Grant
- 2014-10-30 WO PCT/EP2014/073368 patent/WO2015067524A1/en not_active Ceased
- 2014-10-30 EP EP14790645.7A patent/EP3065544A1/en not_active Withdrawn
- 2014-10-30 CN CN201480060395.2A patent/CN105682459A/zh active Pending
- 2014-10-30 CA CA2926878A patent/CA2926878C/en active Active
- 2014-10-30 JP JP2016551000A patent/JP6462706B2/ja not_active Expired - Fee Related
-
2016
- 2016-04-11 IL IL245041A patent/IL245041A0/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| CN105682459A (zh) | 2016-06-15 |
| EP3065544A1 (en) | 2016-09-14 |
| JP2016535092A (ja) | 2016-11-10 |
| JP6462706B2 (ja) | 2019-01-30 |
| US20160255830A1 (en) | 2016-09-08 |
| CA2926878A1 (en) | 2015-05-14 |
| WO2015067524A1 (en) | 2015-05-14 |
| IL245041A0 (en) | 2016-05-31 |
| RU2665099C2 (ru) | 2018-08-28 |
| BR112016009977B1 (pt) | 2020-05-05 |
| RU2016121720A (ru) | 2017-12-11 |
| US20170295779A9 (en) | 2017-10-19 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| EEER | Examination request |
Effective date: 20191028 |
|
| EEER | Examination request |
Effective date: 20191028 |