ES2825323T3 - Derivados de aceites naturales maleados como adyuvantes agroquímicos - Google Patents
Derivados de aceites naturales maleados como adyuvantes agroquímicos Download PDFInfo
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- ES2825323T3 ES2825323T3 ES16769367T ES16769367T ES2825323T3 ES 2825323 T3 ES2825323 T3 ES 2825323T3 ES 16769367 T ES16769367 T ES 16769367T ES 16769367 T ES16769367 T ES 16769367T ES 2825323 T3 ES2825323 T3 ES 2825323T3
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- Prior art keywords
- oil
- adjuvant composition
- weight
- pesticide
- maleate
- Prior art date
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- CLKZWXHKFXZIMA-UHFFFAOYSA-N pyrinuron Chemical compound C1=CC([N+](=O)[O-])=CC=C1NC(=O)NCC1=CC=CN=C1 CLKZWXHKFXZIMA-UHFFFAOYSA-N 0.000 description 1
- 150000003856 quaternary ammonium compounds Chemical class 0.000 description 1
- ABOOPXYCKNFDNJ-SNVBAGLBSA-N quizalofop-P Chemical compound C1=CC(O[C@H](C)C(O)=O)=CC=C1OC1=CN=C(C=C(Cl)C=C2)C2=N1 ABOOPXYCKNFDNJ-SNVBAGLBSA-N 0.000 description 1
- BACHBFVBHLGWSL-JTQLQIEISA-N rac-diclofop methyl Natural products C1=CC(O[C@@H](C)C(=O)OC)=CC=C1OC1=CC=C(Cl)C=C1Cl BACHBFVBHLGWSL-JTQLQIEISA-N 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 230000033458 reproduction Effects 0.000 description 1
- MEFOUWRMVYJCQC-UHFFFAOYSA-N rimsulfuron Chemical compound CCS(=O)(=O)C1=CC=CN=C1S(=O)(=O)NC(=O)NC1=NC(OC)=CC(OC)=N1 MEFOUWRMVYJCQC-UHFFFAOYSA-N 0.000 description 1
- 239000010666 rose oil Substances 0.000 description 1
- 235000005713 safflower oil Nutrition 0.000 description 1
- 230000001932 seasonal effect Effects 0.000 description 1
- 235000011803 sesame oil Nutrition 0.000 description 1
- 239000008159 sesame oil Substances 0.000 description 1
- 238000004904 shortening Methods 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 235000020374 simple syrup Nutrition 0.000 description 1
- PTLRDCMBXHILCL-UHFFFAOYSA-M sodium arsenite Chemical compound [Na+].[O-][As]=O PTLRDCMBXHILCL-UHFFFAOYSA-M 0.000 description 1
- JGFYQVQAXANWJU-UHFFFAOYSA-M sodium fluoroacetate Chemical compound [Na+].[O-]C(=O)CF JGFYQVQAXANWJU-UHFFFAOYSA-M 0.000 description 1
- 239000004328 sodium tetraborate Substances 0.000 description 1
- 235000010339 sodium tetraborate Nutrition 0.000 description 1
- NMWCVZCSJHJYFW-UHFFFAOYSA-M sodium;3,5-dichloro-2-hydroxybenzenesulfonate Chemical compound [Na+].OC1=C(Cl)C=C(Cl)C=C1S([O-])(=O)=O NMWCVZCSJHJYFW-UHFFFAOYSA-M 0.000 description 1
- 238000003892 spreading Methods 0.000 description 1
- 230000007480 spreading Effects 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 238000010561 standard procedure Methods 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 239000000021 stimulant Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 150000003445 sucroses Chemical class 0.000 description 1
- PQTBTIFWAXVEPB-UHFFFAOYSA-N sulcotrione Chemical compound ClC1=CC(S(=O)(=O)C)=CC=C1C(=O)C1C(=O)CCCC1=O PQTBTIFWAXVEPB-UHFFFAOYSA-N 0.000 description 1
- 125000001273 sulfonato group Chemical group [O-]S(*)(=O)=O 0.000 description 1
- 239000002600 sunflower oil Substances 0.000 description 1
- 235000020238 sunflower seed Nutrition 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 235000012222 talc Nutrition 0.000 description 1
- RJKCKKDSSSRYCB-UHFFFAOYSA-N tebutam Chemical compound CC(C)(C)C(=O)N(C(C)C)CC1=CC=CC=C1 RJKCKKDSSSRYCB-UHFFFAOYSA-N 0.000 description 1
- CJDWRQLODFKPEL-UHFFFAOYSA-N teflubenzuron Chemical compound FC1=CC=CC(F)=C1C(=O)NC(=O)NC1=CC(Cl)=C(F)C(Cl)=C1F CJDWRQLODFKPEL-UHFFFAOYSA-N 0.000 description 1
- IROINLKCQGIITA-UHFFFAOYSA-N terbutryn Chemical compound CCNC1=NC(NC(C)(C)C)=NC(SC)=N1 IROINLKCQGIITA-UHFFFAOYSA-N 0.000 description 1
- FZXISNSWEXTPMF-UHFFFAOYSA-N terbutylazine Chemical compound CCNC1=NC(Cl)=NC(NC(C)(C)C)=N1 FZXISNSWEXTPMF-UHFFFAOYSA-N 0.000 description 1
- CXWXQJXEFPUFDZ-UHFFFAOYSA-N tetralin Chemical compound C1=CC=C2CCCCC2=C1 CXWXQJXEFPUFDZ-UHFFFAOYSA-N 0.000 description 1
- 229910052716 thallium Inorganic materials 0.000 description 1
- BKVIYDNLLOSFOA-UHFFFAOYSA-N thallium Chemical compound [Tl] BKVIYDNLLOSFOA-UHFFFAOYSA-N 0.000 description 1
- 239000004308 thiabendazole Substances 0.000 description 1
- WJCNZQLZVWNLKY-UHFFFAOYSA-N thiabendazole Chemical compound S1C=NC(C=2NC3=CC=CC=C3N=2)=C1 WJCNZQLZVWNLKY-UHFFFAOYSA-N 0.000 description 1
- 235000010296 thiabendazole Nutrition 0.000 description 1
- 229960004546 thiabendazole Drugs 0.000 description 1
- 229960002447 thiram Drugs 0.000 description 1
- KUAZQDVKQLNFPE-UHFFFAOYSA-N thiram Chemical compound CN(C)C(=S)SSC(=S)N(C)C KUAZQDVKQLNFPE-UHFFFAOYSA-N 0.000 description 1
- 239000010496 thistle oil Substances 0.000 description 1
- 239000011135 tin Substances 0.000 description 1
- 229910052718 tin Inorganic materials 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- 229930003799 tocopherol Natural products 0.000 description 1
- 235000010384 tocopherol Nutrition 0.000 description 1
- 229960001295 tocopherol Drugs 0.000 description 1
- 239000011732 tocopherol Substances 0.000 description 1
- OBZIQQJJIKNWNO-UHFFFAOYSA-N tolclofos-methyl Chemical group COP(=S)(OC)OC1=C(Cl)C=C(C)C=C1Cl OBZIQQJJIKNWNO-UHFFFAOYSA-N 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- DQFPEYARZIQXRM-LTGZKZEYSA-N tralkoxydim Chemical compound C1C(=O)C(C(/CC)=N/OCC)=C(O)CC1C1=C(C)C=C(C)C=C1C DQFPEYARZIQXRM-LTGZKZEYSA-N 0.000 description 1
- MAZWDMBCPDUFDJ-UHFFFAOYSA-N trans-Traumatinsaeure Natural products OC(=O)CCCCCCCCC=CC(O)=O MAZWDMBCPDUFDJ-UHFFFAOYSA-N 0.000 description 1
- GTZCVFVGUGFEME-UHFFFAOYSA-N trans-aconitic acid Natural products OC(=O)CC(C(O)=O)=CC(O)=O GTZCVFVGUGFEME-UHFFFAOYSA-N 0.000 description 1
- MAZWDMBCPDUFDJ-VQHVLOKHSA-N traumatic acid Chemical compound OC(=O)CCCCCCCC\C=C\C(O)=O MAZWDMBCPDUFDJ-VQHVLOKHSA-N 0.000 description 1
- XOPFESVZMSQIKC-UHFFFAOYSA-N triasulfuron Chemical compound COC1=NC(C)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2)OCCCl)=N1 XOPFESVZMSQIKC-UHFFFAOYSA-N 0.000 description 1
- 150000003852 triazoles Chemical class 0.000 description 1
- ONCZDRURRATYFI-TVJDWZFNSA-N trifloxystrobin Chemical compound CO\N=C(\C(=O)OC)C1=CC=CC=C1CO\N=C(/C)C1=CC=CC(C(F)(F)F)=C1 ONCZDRURRATYFI-TVJDWZFNSA-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
- PHYFQTYBJUILEZ-IUPFWZBJSA-N triolein Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OCC(OC(=O)CCCCCCC\C=C/CCCCCCCC)COC(=O)CCCCCCC\C=C/CCCCCCCC PHYFQTYBJUILEZ-IUPFWZBJSA-N 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 235000001892 vitamin D2 Nutrition 0.000 description 1
- 239000011653 vitamin D2 Substances 0.000 description 1
- MECHNRXZTMCUDQ-RKHKHRCZSA-N vitamin D2 Chemical compound C1(/[C@@H]2CC[C@@H]([C@]2(CCC1)C)[C@H](C)/C=C/[C@H](C)C(C)C)=C\C=C1\C[C@@H](O)CCC1=C MECHNRXZTMCUDQ-RKHKHRCZSA-N 0.000 description 1
- 235000005282 vitamin D3 Nutrition 0.000 description 1
- 239000011647 vitamin D3 Substances 0.000 description 1
- QYSXJUFSXHHAJI-YRZJJWOYSA-N vitamin D3 Chemical compound C1(/[C@@H]2CC[C@@H]([C@]2(CCC1)C)[C@H](C)CCCC(C)C)=C\C=C1\C[C@@H](O)CCC1=C QYSXJUFSXHHAJI-YRZJJWOYSA-N 0.000 description 1
- 235000019165 vitamin E Nutrition 0.000 description 1
- 239000011709 vitamin E Substances 0.000 description 1
- 229940046009 vitamin E Drugs 0.000 description 1
- 229940021056 vitamin d3 Drugs 0.000 description 1
- 235000020234 walnut Nutrition 0.000 description 1
- 239000008170 walnut oil Substances 0.000 description 1
- 229960005080 warfarin Drugs 0.000 description 1
- PJVWKTKQMONHTI-UHFFFAOYSA-N warfarin Chemical compound OC=1C2=CC=CC=C2OC(=O)C=1C(CC(=O)C)C1=CC=CC=C1 PJVWKTKQMONHTI-UHFFFAOYSA-N 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
- 125000000969 xylosyl group Chemical group C1([C@H](O)[C@@H](O)[C@H](O)CO1)* 0.000 description 1
- 229940048462 zinc phosphide Drugs 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
- 239000004711 α-olefin Substances 0.000 description 1
- GVJHHUAWPYXKBD-IEOSBIPESA-N α-tocopherol Chemical compound OC1=C(C)C(C)=C2O[C@@](CCC[C@H](C)CCC[C@H](C)CCCC(C)C)(C)CCC2=C1C GVJHHUAWPYXKBD-IEOSBIPESA-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
-
- 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
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/36—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a singly bound oxygen or sulfur atom attached to the same carbon skeleton, this oxygen or sulfur atom not being a member of a carboxylic group or of a thio analogue, or of a derivative thereof, e.g. hydroxy-carboxylic acids
- A01N37/38—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a singly bound oxygen or sulfur atom attached to the same carbon skeleton, this oxygen or sulfur atom not being a member of a carboxylic group or of a thio analogue, or of a derivative thereof, e.g. hydroxy-carboxylic acids having at least one oxygen or sulfur atom attached to an aromatic ring system
- A01N37/40—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a singly bound oxygen or sulfur atom attached to the same carbon skeleton, this oxygen or sulfur atom not being a member of a carboxylic group or of a thio analogue, or of a derivative thereof, e.g. hydroxy-carboxylic acids having at least one oxygen or sulfur atom attached to an aromatic ring system having at least one carboxylic group or a thio analogue, or a derivative thereof, and one oxygen or sulfur atom attached to the same aromatic ring system
-
- 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
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
- A01N43/54—1,3-Diazines; Hydrogenated 1,3-diazines
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N57/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds
- A01N57/18—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-carbon bonds
- A01N57/20—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-carbon bonds containing acyclic or cycloaliphatic radicals
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N65/00—Biocides, pest repellants or attractants, or plant growth regulators containing material from algae, lichens, bryophyta, multi-cellular fungi or plants, or extracts thereof
- A01N65/08—Magnoliopsida [dicotyledons]
- A01N65/20—Fabaceae or Leguminosae [Pea or Legume family], e.g. pea, lentil, soybean, clover, acacia, honey locust, derris or millettia
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Zoology (AREA)
- Dentistry (AREA)
- Agronomy & Crop Science (AREA)
- Environmental Sciences (AREA)
- Wood Science & Technology (AREA)
- Plant Pathology (AREA)
- Pest Control & Pesticides (AREA)
- Natural Medicines & Medicinal Plants (AREA)
- Mycology (AREA)
- Microbiology (AREA)
- Biotechnology (AREA)
- Toxicology (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201562137886P | 2015-03-25 | 2015-03-25 | |
| PCT/US2016/022840 WO2016153913A1 (en) | 2015-03-25 | 2016-03-17 | Maleated natural oil derivatives as agrochemical inert ingredients |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES2825323T3 true ES2825323T3 (es) | 2021-05-17 |
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| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES16769367T Active ES2825323T3 (es) | 2015-03-25 | 2016-03-17 | Derivados de aceites naturales maleados como adyuvantes agroquímicos |
Country Status (10)
| Country | Link |
|---|---|
| US (2) | US20180070584A1 (enExample) |
| EP (1) | EP3285585B1 (enExample) |
| JP (1) | JP7039293B2 (enExample) |
| CN (1) | CN107404872B (enExample) |
| AU (1) | AU2016235791A1 (enExample) |
| BR (1) | BR112017020250B1 (enExample) |
| CA (1) | CA2979539C (enExample) |
| ES (1) | ES2825323T3 (enExample) |
| MX (1) | MX390655B (enExample) |
| WO (1) | WO2016153913A1 (enExample) |
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| US11208612B2 (en) * | 2017-12-08 | 2021-12-28 | The Lubrizol Corporation | Maleated soybean oil derivatives as additives in metalworking fluids |
| CN109090108B (zh) * | 2018-09-13 | 2021-03-02 | 江苏擎宇化工科技有限公司 | 一种乳化植物油乳化剂组合物及其制备方法 |
| IT201800010481A1 (it) | 2018-11-23 | 2020-05-23 | Lamberti Spa | Dispersioni in olio di ditiocarbammati |
| WO2020172001A1 (en) * | 2019-02-21 | 2020-08-27 | Huntsman Petrochemical Llc | Multifunctional additive compounds |
| CN110692632B (zh) * | 2019-09-04 | 2022-02-08 | 深圳诺普信农化股份有限公司 | 一种用于磺酰脲类除草剂的稳定剂及其制备方法和应用 |
| IT202000004816A1 (it) * | 2020-03-06 | 2021-09-06 | Alpha Biopesticides Ltd | Composizione pesticida per la cura e la protezione delle coltivazioni |
| US20220167613A1 (en) * | 2020-12-01 | 2022-06-02 | Stratacor, Inc. | Choline chloride adjuvant for fatty acid based biopesticide |
| US11760952B2 (en) * | 2021-01-12 | 2023-09-19 | Ingevity South Carolina, Llc | Lubricant thickener systems from modified tall oil fatty acids, lubricating compositions, and associated methods |
| CN118302488A (zh) * | 2021-09-20 | 2024-07-05 | 埃斯普投资有限公司 | 疏水改性的和亲水改性的马来化天然油及其组合物 |
| AU2022383779A1 (en) * | 2021-11-02 | 2024-05-02 | Isp Investments Llc | Hydrophobic and hydrophilic modified maleated natural oils, salts, compositions, and methods of use |
| EP4532608A1 (en) * | 2022-05-31 | 2025-04-09 | ISP Investments LLC | Hydrophobic and hydrophilic modified maleated natural oils and compositions thereof |
| AR130822A1 (es) * | 2022-10-20 | 2025-01-22 | Dva Agro Gmbh | Composición de microemulsión de saflufenacil, su proceso de preparación y uso |
| CN121174941A (zh) * | 2023-03-22 | 2025-12-19 | 埃斯普投资有限公司 | 疏水改性的和亲水改性的马来化天然油及其农业组合物 |
| WO2024229189A2 (en) * | 2023-05-02 | 2024-11-07 | Isp Investments Llc | Hydrophobic and hydrophilic modified maleated natural oils, salts and its agricultural compositions and methods of use |
| AR133425A1 (es) * | 2023-07-31 | 2025-09-24 | Championx Llc | Composiciones y métodos de uso de amidas grasas maleadas de polieteraminas para inhibir la corrosión |
| WO2025059059A1 (en) * | 2023-09-11 | 2025-03-20 | Isp Investments Llc | Slurry compositions comprising modified natural oil salts, processes for preparing, and applications thereof |
| WO2025059043A1 (en) * | 2023-09-11 | 2025-03-20 | Isp Investments Llc | A modified maleated natural oil containing a lactam moiety, salts, compositions, and use thereof |
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| US2033131A (en) * | 1931-07-07 | 1936-03-10 | Ellis Foster Co | Reaction product and process of making same |
| US2033132A (en) * | 1931-08-07 | 1936-03-10 | Ellis Foster Co | Diene type reaction product and method of making same |
| US2188882A (en) | 1934-12-24 | 1940-01-30 | Edwin T Clocker | Condensation product and method |
| US2188887A (en) | 1938-09-26 | 1940-01-30 | Edwin T Clocker | Oily dispersion material |
| US3412053A (en) * | 1964-07-06 | 1968-11-19 | Huber Corp J M | Printing inks and varnishes |
| US3600186A (en) | 1968-04-23 | 1971-08-17 | Procter & Gamble | Low calorie fat-containing food compositions |
| US3654370A (en) | 1970-08-28 | 1972-04-04 | Jefferson Chem Co Inc | Process for preparing polyoxyalkylene polyamines |
| US3832402A (en) | 1970-12-08 | 1974-08-27 | Jefferson Chem Co Inc | Tertiary polyoxyalkylenepolyamines |
| US4990476A (en) | 1979-10-15 | 1991-02-05 | Union Oil Company Of California | Hydrocarbon conversion catalyst for use in selectively making middle distillates |
| US4992590A (en) | 1989-10-02 | 1991-02-12 | Texaco Chemical Company | Polyamines by amination of polyamino initiated polyoxyalkylene glycols |
| US5521144A (en) | 1992-09-18 | 1996-05-28 | Central Soya Company, Inc. | Herbicide composition |
| GB9412722D0 (en) | 1994-06-24 | 1994-08-17 | Zeneca Ltd | Herbicidal composition |
| US5495033A (en) | 1994-08-29 | 1996-02-27 | Cenex/Land O'lakes Agronomy Company | Methylated herbicidal adjuvant |
| US5658855A (en) | 1996-09-26 | 1997-08-19 | North Dakota State University | Adjuvants for herbicidal compositions |
| US5942542A (en) | 1996-09-29 | 1999-08-24 | Victorian Chemical International Pty Ltd. | Insecticide adjuvants |
| US5928563A (en) | 1997-06-20 | 1999-07-27 | Henkel Corporation | Agricultural adjuvant |
| US6239298B1 (en) * | 1998-05-26 | 2001-05-29 | International Lubricants Inc. | Fuel lubricity additives |
| US6642178B2 (en) | 2001-11-14 | 2003-11-04 | North Dakota State University | Adjuvant blend for enhancing efficacy of pesticides |
| US6689720B2 (en) | 2001-11-14 | 2004-02-10 | Ndsu-Research Foundation | High-pH oil based adjuvant blend for enhancing efficacy of pesticides |
| DE60215558T2 (de) | 2002-04-17 | 2007-08-02 | Agribiotec S.R.L. | Benutzung von pflanzlichem öl als adjuvantien für fungizide, bakterizide, insektizide oder herbizide substanzen |
| US8138120B2 (en) | 2003-03-11 | 2012-03-20 | Cognis Ip Management Gmbh | Microemulsions as adjuvants for agricultural chemicals |
| JP5078126B2 (ja) | 2004-01-09 | 2012-11-21 | ザ ルブリゾル コーポレイション | 金属加工における自己乳化潤滑油としてのマレイン酸化植物油および誘導体 |
| CA2704147C (en) * | 2007-07-03 | 2015-08-11 | Georgia-Pacific Chemicals Llc | Chemical modification of maleated fatty acids |
| EP2181594A1 (en) | 2008-10-28 | 2010-05-05 | Cognis IP Management GmbH | Agricultural compositions |
| AR075294A1 (es) * | 2008-10-31 | 2011-03-23 | Dow Agrosciences Llc | Control de la dispersion de la pulverizacion de pesticidas con esteres auto emulsificables |
| US20130210630A1 (en) | 2010-07-02 | 2013-08-15 | Isp Investments Inc. | Self-emulsifying oil |
| US9809538B2 (en) * | 2010-07-26 | 2017-11-07 | Isp Investments Llc | Renewable modified natural compounds |
| CA2869303C (en) * | 2012-02-25 | 2020-03-24 | Ethox Chemicals, Llc | Natural oil based gels, applications and methods of preparation |
| RU2663171C2 (ru) * | 2012-09-19 | 2018-08-01 | Акцо Нобель Коатингс Интернэшнл Б.В. | Водные композиции для покрытия, включающие в себя продукт реакции малеинового ангидрида с ненасыщенным соединением и амином |
| JP6595978B2 (ja) * | 2013-03-15 | 2019-10-23 | エトクス ケミカルズ リミテッド ライアビリティ カンパニー | バイオベース分散剤 |
| WO2014200671A2 (en) * | 2013-06-12 | 2014-12-18 | Meadwestvaco Corporation | Clay inhibitors for drilling, fracturing, and other procedures |
-
2016
- 2016-03-17 US US15/559,227 patent/US20180070584A1/en not_active Abandoned
- 2016-03-17 MX MX2017012207A patent/MX390655B/es unknown
- 2016-03-17 WO PCT/US2016/022840 patent/WO2016153913A1/en not_active Ceased
- 2016-03-17 EP EP16769367.0A patent/EP3285585B1/en active Active
- 2016-03-17 JP JP2017549412A patent/JP7039293B2/ja active Active
- 2016-03-17 ES ES16769367T patent/ES2825323T3/es active Active
- 2016-03-17 AU AU2016235791A patent/AU2016235791A1/en not_active Abandoned
- 2016-03-17 CN CN201680017951.7A patent/CN107404872B/zh active Active
- 2016-03-17 BR BR112017020250-6A patent/BR112017020250B1/pt active IP Right Grant
- 2016-03-17 CA CA2979539A patent/CA2979539C/en active Active
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2024
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Also Published As
| Publication number | Publication date |
|---|---|
| AU2016235791A1 (en) | 2017-09-21 |
| MX2017012207A (es) | 2018-01-23 |
| MX390655B (es) | 2025-03-21 |
| JP2018513131A (ja) | 2018-05-24 |
| CA2979539A1 (en) | 2016-09-29 |
| JP7039293B2 (ja) | 2022-03-22 |
| EP3285585A1 (en) | 2018-02-28 |
| CA2979539C (en) | 2023-02-14 |
| EP3285585B1 (en) | 2020-08-19 |
| CN107404872B (zh) | 2020-11-10 |
| WO2016153913A1 (en) | 2016-09-29 |
| BR112017020250A2 (pt) | 2018-06-12 |
| BR112017020250B1 (pt) | 2021-11-23 |
| US20250057153A1 (en) | 2025-02-20 |
| EP3285585A4 (en) | 2018-09-19 |
| CN107404872A (zh) | 2017-11-28 |
| US20180070584A1 (en) | 2018-03-15 |
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