CA2979539C - Maleated natural oil derivatives as agrochemical inert ingredients - Google Patents
Maleated natural oil derivatives as agrochemical inert ingredients Download PDFInfo
- Publication number
- CA2979539C CA2979539C CA2979539A CA2979539A CA2979539C CA 2979539 C CA2979539 C CA 2979539C CA 2979539 A CA2979539 A CA 2979539A CA 2979539 A CA2979539 A CA 2979539A CA 2979539 C CA2979539 C CA 2979539C
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- Prior art keywords
- oil
- maleated
- adjuvant composition
- weight
- pesticide
- Prior art date
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- 239000003905 agrochemical Substances 0.000 title claims abstract description 49
- 229940060367 inert ingredients Drugs 0.000 title description 7
- 239000000203 mixture Substances 0.000 claims abstract description 222
- 239000002671 adjuvant Substances 0.000 claims abstract description 90
- 238000009472 formulation Methods 0.000 claims abstract description 70
- 241000607479 Yersinia pestis Species 0.000 claims abstract description 15
- 235000019198 oils Nutrition 0.000 claims description 103
- 239000003921 oil Substances 0.000 claims description 101
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 67
- 239000000194 fatty acid Substances 0.000 claims description 67
- 229930195729 fatty acid Natural products 0.000 claims description 67
- 239000000575 pesticide Substances 0.000 claims description 67
- 150000004665 fatty acids Chemical class 0.000 claims description 48
- 150000001875 compounds Chemical class 0.000 claims description 33
- 239000012141 concentrate Substances 0.000 claims description 28
- 239000007921 spray Substances 0.000 claims description 23
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 22
- 235000015112 vegetable and seed oil Nutrition 0.000 claims description 18
- 239000004009 herbicide Substances 0.000 claims description 17
- 238000000034 method Methods 0.000 claims description 17
- 238000006243 chemical reaction Methods 0.000 claims description 13
- 150000008064 anhydrides Chemical class 0.000 claims description 12
- 239000002904 solvent Substances 0.000 claims description 12
- 235000012424 soybean oil Nutrition 0.000 claims description 11
- 239000003549 soybean oil Substances 0.000 claims description 11
- 229920000570 polyether Polymers 0.000 claims description 10
- 239000008158 vegetable oil Substances 0.000 claims description 10
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- 125000005907 alkyl ester group Chemical group 0.000 claims description 6
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- 230000000855 fungicidal effect Effects 0.000 claims description 3
- 239000003750 molluscacide Substances 0.000 claims description 3
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- 239000003090 pesticide formulation Substances 0.000 claims description 2
- 239000000758 substrate Substances 0.000 abstract description 16
- -1 ammonia compound Chemical class 0.000 description 58
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- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 19
- XDDAORKBJWWYJS-UHFFFAOYSA-N glyphosate Chemical compound OC(=O)CNCP(O)(O)=O XDDAORKBJWWYJS-UHFFFAOYSA-N 0.000 description 16
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- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 11
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- 229910000000 metal hydroxide Inorganic materials 0.000 description 11
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- CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 description 10
- 229930006000 Sucrose Natural products 0.000 description 10
- UYMKPFRHYYNDTL-UHFFFAOYSA-N ethenamine Chemical compound NC=C UYMKPFRHYYNDTL-UHFFFAOYSA-N 0.000 description 10
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- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 9
- 125000000217 alkyl group Chemical group 0.000 description 9
- 239000000047 product Substances 0.000 description 9
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- 239000001257 hydrogen Substances 0.000 description 8
- 229910052739 hydrogen Inorganic materials 0.000 description 8
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- 241000196324 Embryophyta Species 0.000 description 7
- 239000002253 acid Substances 0.000 description 7
- 229910021529 ammonia Inorganic materials 0.000 description 7
- 230000000694 effects Effects 0.000 description 7
- 238000002156 mixing Methods 0.000 description 7
- 150000003839 salts Chemical class 0.000 description 7
- YIWUKEYIRIRTPP-UHFFFAOYSA-N 2-ethylhexanol Substances CCCCC(CC)CO YIWUKEYIRIRTPP-UHFFFAOYSA-N 0.000 description 6
- UIKUBYKUYUSRSM-UHFFFAOYSA-N 3-morpholinopropylamine Chemical compound NCCCN1CCOCC1 UIKUBYKUYUSRSM-UHFFFAOYSA-N 0.000 description 6
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Natural products OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 6
- 150000001298 alcohols Chemical class 0.000 description 6
- 239000003795 chemical substances by application Substances 0.000 description 6
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 6
- 239000003925 fat Substances 0.000 description 6
- 235000019197 fats Nutrition 0.000 description 6
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 6
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 6
- 235000008390 olive oil Nutrition 0.000 description 6
- 239000004006 olive oil Substances 0.000 description 6
- 229920001223 polyethylene glycol Polymers 0.000 description 6
- GNHDVXLWBQYPJE-UHFFFAOYSA-N saflufenacil Chemical compound C1=C(Cl)C(C(=O)NS(=O)(=O)N(C)C(C)C)=CC(N2C(N(C)C(=CC2=O)C(F)(F)F)=O)=C1F GNHDVXLWBQYPJE-UHFFFAOYSA-N 0.000 description 6
- 150000005846 sugar alcohols Chemical class 0.000 description 6
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical class OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 5
- 125000004432 carbon atom Chemical group C* 0.000 description 5
- 239000000969 carrier Substances 0.000 description 5
- 239000003086 colorant Substances 0.000 description 5
- 239000003337 fertilizer Substances 0.000 description 5
- 239000004615 ingredient Substances 0.000 description 5
- 150000002772 monosaccharides Chemical class 0.000 description 5
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 5
- 229920000642 polymer Polymers 0.000 description 5
- 235000021122 unsaturated fatty acids Nutrition 0.000 description 5
- 150000004670 unsaturated fatty acids Chemical class 0.000 description 5
- VILCJCGEZXAXTO-UHFFFAOYSA-N 2,2,2-tetramine Chemical compound NCCNCCNCCN VILCJCGEZXAXTO-UHFFFAOYSA-N 0.000 description 4
- POAOYUHQDCAZBD-UHFFFAOYSA-N 2-butoxyethanol Chemical compound CCCCOCCO POAOYUHQDCAZBD-UHFFFAOYSA-N 0.000 description 4
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 4
- 239000005504 Dicamba Substances 0.000 description 4
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 4
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 4
- 244000068988 Glycine max Species 0.000 description 4
- 241001465754 Metazoa Species 0.000 description 4
- GLUUGHFHXGJENI-UHFFFAOYSA-N Piperazine Chemical compound C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 description 4
- 239000002202 Polyethylene glycol Substances 0.000 description 4
- 229920002125 Sokalan® Polymers 0.000 description 4
- 235000005687 corn oil Nutrition 0.000 description 4
- 239000002285 corn oil Substances 0.000 description 4
- IWEDIXLBFLAXBO-UHFFFAOYSA-N dicamba Chemical compound COC1=C(Cl)C=CC(Cl)=C1C(O)=O IWEDIXLBFLAXBO-UHFFFAOYSA-N 0.000 description 4
- 238000002474 experimental method Methods 0.000 description 4
- 230000000670 limiting effect Effects 0.000 description 4
- 235000012054 meals Nutrition 0.000 description 4
- 239000000600 sorbitol Substances 0.000 description 4
- 239000003760 tallow Substances 0.000 description 4
- FAGUFWYHJQFNRV-UHFFFAOYSA-N tetraethylenepentamine Chemical compound NCCNCCNCCNCCN FAGUFWYHJQFNRV-UHFFFAOYSA-N 0.000 description 4
- IMNIMPAHZVJRPE-UHFFFAOYSA-N triethylenediamine Chemical compound C1CN2CCN1CC2 IMNIMPAHZVJRPE-UHFFFAOYSA-N 0.000 description 4
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 3
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 3
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 3
- 240000006162 Chenopodium quinoa Species 0.000 description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 3
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 3
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- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 3
- 235000010469 Glycine max Nutrition 0.000 description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-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
- 239000005642 Oleic acid Substances 0.000 description 3
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 3
- 235000019483 Peanut oil Nutrition 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
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- TVXBFESIOXBWNM-UHFFFAOYSA-N Xylitol Natural products OCCC(O)C(O)C(O)CCO TVXBFESIOXBWNM-UHFFFAOYSA-N 0.000 description 3
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- 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
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- 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
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- 229940021056 vitamin d3 Drugs 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
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- 239000008096 xylene Substances 0.000 description 1
- 150000003738 xylenes Chemical class 0.000 description 1
- 125000000969 xylosyl group Chemical group C1([C@H](O)[C@@H](O)[C@H](O)CO1)* 0.000 description 1
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- 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
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- 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 (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201562137886P | 2015-03-25 | 2015-03-25 | |
| US62/137,886 | 2015-03-25 | ||
| PCT/US2016/022840 WO2016153913A1 (en) | 2015-03-25 | 2016-03-17 | Maleated natural oil derivatives as agrochemical inert ingredients |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CA2979539A1 CA2979539A1 (en) | 2016-09-29 |
| CA2979539C true CA2979539C (en) | 2023-02-14 |
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|---|---|---|---|
| CA2979539A Active CA2979539C (en) | 2015-03-25 | 2016-03-17 | Maleated natural oil derivatives as agrochemical inert ingredients |
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) |
Families Citing this family (17)
| Publication number | Priority date | Publication date | Assignee | Title |
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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
-
2024
- 2024-11-01 US US18/935,034 patent/US20250057153A1/en active Pending
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 |
| 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 |
| ES2825323T3 (es) | 2021-05-17 |
| US20180070584A1 (en) | 2018-03-15 |
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