EA011649B1 - Композиция на основе алкоксилатов спиртов и их применение в качестве адъюванта в области агротехники - Google Patents
Композиция на основе алкоксилатов спиртов и их применение в качестве адъюванта в области агротехники Download PDFInfo
- Publication number
- EA011649B1 EA011649B1 EA200401383A EA200401383A EA011649B1 EA 011649 B1 EA011649 B1 EA 011649B1 EA 200401383 A EA200401383 A EA 200401383A EA 200401383 A EA200401383 A EA 200401383A EA 011649 B1 EA011649 B1 EA 011649B1
- Authority
- EA
- Eurasian Patent Office
- Prior art keywords
- value
- composition according
- takes
- alkoxylates
- composition
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 84
- 239000002671 adjuvant Substances 0.000 title claims abstract description 17
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 title description 11
- -1 2-propylheptyl Chemical group 0.000 claims abstract description 54
- 239000004480 active ingredient Substances 0.000 claims abstract description 26
- YLQLIQIAXYRMDL-UHFFFAOYSA-N propylheptyl alcohol Chemical compound CCCCCC(CO)CCC YLQLIQIAXYRMDL-UHFFFAOYSA-N 0.000 claims abstract description 10
- 239000005476 Bentazone Substances 0.000 claims description 6
- 239000000654 additive Substances 0.000 claims description 6
- ZOMSMJKLGFBRBS-UHFFFAOYSA-N bentazone Chemical group C1=CC=C2NS(=O)(=O)N(C(C)C)C(=O)C2=C1 ZOMSMJKLGFBRBS-UHFFFAOYSA-N 0.000 claims description 6
- CNBGNNVCVSKAQZ-UHFFFAOYSA-N benzidamine Natural products C12=CC=CC=C2C(OCCCN(C)C)=NN1CC1=CC=CC=C1 CNBGNNVCVSKAQZ-UHFFFAOYSA-N 0.000 claims description 6
- 239000005629 Tritosulfuron Substances 0.000 claims description 5
- 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 claims description 5
- ZMYFCFLJBGAQRS-IAGOWNOFSA-N (2S,3R)-epoxiconazole Chemical compound C1=CC(F)=CC=C1[C@]1(CN2N=CN=C2)[C@@H](C=2C(=CC=CC=2)Cl)O1 ZMYFCFLJBGAQRS-IAGOWNOFSA-N 0.000 claims description 2
- QNBTYORWCCMPQP-JXAWBTAJSA-N (Z)-dimethomorph Chemical compound C1=C(OC)C(OC)=CC=C1C(\C=1C=CC(Cl)=CC=1)=C/C(=O)N1CCOCC1 QNBTYORWCCMPQP-JXAWBTAJSA-N 0.000 claims description 2
- 239000005761 Dimethomorph Substances 0.000 claims description 2
- 239000005800 Kresoxim-methyl Substances 0.000 claims description 2
- 239000005868 Metconazole Substances 0.000 claims description 2
- 239000005869 Pyraclostrobin Substances 0.000 claims description 2
- 239000013543 active substance Substances 0.000 claims description 2
- 230000000996 additive effect Effects 0.000 claims description 2
- 238000003898 horticulture Methods 0.000 claims description 2
- ZOTBXTZVPHCKPN-HTXNQAPBSA-N kresoxim-methyl Chemical compound CO\N=C(\C(=O)OC)C1=CC=CC=C1COC1=CC=CC=C1C ZOTBXTZVPHCKPN-HTXNQAPBSA-N 0.000 claims description 2
- XWPZUHJBOLQNMN-UHFFFAOYSA-N metconazole Chemical compound C1=NC=NN1CC1(O)C(C)(C)CCC1CC1=CC=C(Cl)C=C1 XWPZUHJBOLQNMN-UHFFFAOYSA-N 0.000 claims description 2
- 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 claims description 2
- 238000005507 spraying Methods 0.000 claims 1
- 150000001298 alcohols Chemical class 0.000 abstract description 24
- 238000010521 absorption reaction Methods 0.000 abstract description 4
- 239000004435 Oxo alcohol Substances 0.000 abstract description 3
- 239000004094 surface-active agent Substances 0.000 description 28
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 18
- 241000196324 Embryophyta Species 0.000 description 15
- 238000006243 chemical reaction Methods 0.000 description 12
- 239000003921 oil Substances 0.000 description 12
- SYURNNNQIFDVCA-UHFFFAOYSA-N 2-propyloxirane Chemical compound CCCC1CO1 SYURNNNQIFDVCA-UHFFFAOYSA-N 0.000 description 11
- 235000019198 oils Nutrition 0.000 description 11
- 230000000694 effects Effects 0.000 description 9
- 239000000126 substance Substances 0.000 description 9
- 239000003085 diluting agent Substances 0.000 description 8
- 239000002904 solvent Substances 0.000 description 8
- 125000002947 alkylene group Chemical group 0.000 description 7
- 150000002148 esters Chemical class 0.000 description 7
- 150000002430 hydrocarbons Chemical class 0.000 description 7
- 239000002736 nonionic surfactant Substances 0.000 description 7
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 6
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 6
- 239000003054 catalyst Substances 0.000 description 6
- 238000000034 method Methods 0.000 description 6
- 238000012545 processing Methods 0.000 description 6
- 125000000217 alkyl group Chemical group 0.000 description 5
- 239000000010 aprotic solvent Substances 0.000 description 5
- 230000018044 dehydration Effects 0.000 description 5
- 238000006297 dehydration reaction Methods 0.000 description 5
- 235000014113 dietary fatty acids Nutrition 0.000 description 5
- 238000007046 ethoxylation reaction Methods 0.000 description 5
- 239000000194 fatty acid Substances 0.000 description 5
- 229930195729 fatty acid Natural products 0.000 description 5
- 238000003756 stirring Methods 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- XUJLWPFSUCHPQL-UHFFFAOYSA-N 11-methyldodecan-1-ol Chemical compound CC(C)CCCCCCCCCCO XUJLWPFSUCHPQL-UHFFFAOYSA-N 0.000 description 4
- PLLBRTOLHQQAQQ-UHFFFAOYSA-N 8-methylnonan-1-ol Chemical compound CC(C)CCCCCCCO PLLBRTOLHQQAQQ-UHFFFAOYSA-N 0.000 description 4
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 4
- 239000002253 acid Substances 0.000 description 4
- 150000007513 acids Chemical group 0.000 description 4
- 230000003213 activating effect Effects 0.000 description 4
- 125000003158 alcohol group Chemical group 0.000 description 4
- 125000003118 aryl group Chemical group 0.000 description 4
- 239000002585 base Substances 0.000 description 4
- 239000012141 concentrate Substances 0.000 description 4
- 238000000227 grinding Methods 0.000 description 4
- 229930195733 hydrocarbon Natural products 0.000 description 4
- 239000004615 ingredient Substances 0.000 description 4
- 150000003254 radicals Chemical class 0.000 description 4
- 239000007921 spray Substances 0.000 description 4
- 239000000021 stimulant Substances 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 239000003945 anionic surfactant Substances 0.000 description 3
- 239000002518 antifoaming agent Substances 0.000 description 3
- 125000004432 carbon atom Chemical group C* 0.000 description 3
- 239000004359 castor oil Substances 0.000 description 3
- 235000019438 castor oil Nutrition 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 229920001577 copolymer Polymers 0.000 description 3
- 150000004665 fatty acids Chemical class 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
- 150000004820 halides Chemical class 0.000 description 3
- 239000004009 herbicide Substances 0.000 description 3
- 229910052500 inorganic mineral Inorganic materials 0.000 description 3
- 150000002576 ketones Chemical class 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 239000011707 mineral Substances 0.000 description 3
- 235000010755 mineral Nutrition 0.000 description 3
- 239000002480 mineral oil Substances 0.000 description 3
- 239000003607 modifier Substances 0.000 description 3
- 150000002790 naphthalenes Chemical class 0.000 description 3
- 239000006174 pH buffer Substances 0.000 description 3
- 239000000546 pharmaceutical excipient Substances 0.000 description 3
- 229920000642 polymer Polymers 0.000 description 3
- 229940051841 polyoxyethylene ether Drugs 0.000 description 3
- 229920000056 polyoxyethylene ether Polymers 0.000 description 3
- 150000003871 sulfonates Chemical class 0.000 description 3
- 239000000725 suspension Substances 0.000 description 3
- 239000004546 suspension concentrate Substances 0.000 description 3
- 230000002195 synergetic effect Effects 0.000 description 3
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 2
- VBICKXHEKHSIBG-UHFFFAOYSA-N 1-monostearoylglycerol Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(O)CO VBICKXHEKHSIBG-UHFFFAOYSA-N 0.000 description 2
- YIWUKEYIRIRTPP-UHFFFAOYSA-N 2-ethylhexan-1-ol Chemical compound CCCCC(CC)CO YIWUKEYIRIRTPP-UHFFFAOYSA-N 0.000 description 2
- YNQLUTRBYVCPMQ-UHFFFAOYSA-N Ethylbenzene Chemical compound CCC1=CC=CC=C1 YNQLUTRBYVCPMQ-UHFFFAOYSA-N 0.000 description 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
- 241001465754 Metazoa Species 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- URLKBWYHVLBVBO-UHFFFAOYSA-N Para-Xylene Chemical group CC1=CC=C(C)C=C1 URLKBWYHVLBVBO-UHFFFAOYSA-N 0.000 description 2
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
- DKGAVHZHDRPRBM-UHFFFAOYSA-N Tert-Butanol Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 description 2
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 2
- 229910052783 alkali metal Inorganic materials 0.000 description 2
- 150000001340 alkali metals Chemical class 0.000 description 2
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 2
- 150000001342 alkaline earth metals Chemical class 0.000 description 2
- 125000005907 alkyl ester group Chemical group 0.000 description 2
- 150000008051 alkyl sulfates Chemical class 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
- 150000003863 ammonium salts Chemical class 0.000 description 2
- 239000002280 amphoteric surfactant Substances 0.000 description 2
- 125000000129 anionic group Chemical group 0.000 description 2
- IAQRGUVFOMOMEM-UHFFFAOYSA-N butene Natural products CC=CC IAQRGUVFOMOMEM-UHFFFAOYSA-N 0.000 description 2
- 239000004202 carbamide Substances 0.000 description 2
- 125000002091 cationic group Chemical group 0.000 description 2
- 239000003093 cationic surfactant Substances 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 235000005687 corn oil Nutrition 0.000 description 2
- 239000002285 corn oil Substances 0.000 description 2
- RWGFKTVRMDUZSP-UHFFFAOYSA-N cumene Chemical compound CC(C)C1=CC=CC=C1 RWGFKTVRMDUZSP-UHFFFAOYSA-N 0.000 description 2
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
- 230000006378 damage Effects 0.000 description 2
- 239000002270 dispersing agent Substances 0.000 description 2
- 238000009826 distribution Methods 0.000 description 2
- 239000004495 emulsifiable concentrate Substances 0.000 description 2
- 239000003995 emulsifying agent Substances 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- 230000007613 environmental effect Effects 0.000 description 2
- 150000002170 ethers Chemical class 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- 239000000284 extract Substances 0.000 description 2
- 239000003925 fat Substances 0.000 description 2
- 235000019197 fats Nutrition 0.000 description 2
- 239000003337 fertilizer Substances 0.000 description 2
- 150000004795 grignard reagents Chemical class 0.000 description 2
- 230000002363 herbicidal effect Effects 0.000 description 2
- 239000003906 humectant Substances 0.000 description 2
- ZXEKIIBDNHEJCQ-UHFFFAOYSA-N isobutanol Chemical compound CC(C)CO ZXEKIIBDNHEJCQ-UHFFFAOYSA-N 0.000 description 2
- 239000000787 lecithin Chemical class 0.000 description 2
- 235000010445 lecithin Nutrition 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 239000004530 micro-emulsion Substances 0.000 description 2
- 235000010446 mineral oil Nutrition 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- TVMXDCGIABBOFY-UHFFFAOYSA-N n-Octanol Natural products CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 2
- PSZYNBSKGUBXEH-UHFFFAOYSA-N naphthalene-1-sulfonic acid Chemical compound C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-N 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 230000035515 penetration Effects 0.000 description 2
- FDPIMTJIUBPUKL-UHFFFAOYSA-N pentan-3-one Chemical compound CCC(=O)CC FDPIMTJIUBPUKL-UHFFFAOYSA-N 0.000 description 2
- 239000002798 polar solvent Substances 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 239000003586 protic polar solvent Substances 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 2
- YTZKOQUCBOVLHL-UHFFFAOYSA-N tert-butylbenzene Chemical compound CC(C)(C)C1=CC=CC=C1 YTZKOQUCBOVLHL-UHFFFAOYSA-N 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- 238000012546 transfer Methods 0.000 description 2
- 239000001993 wax Substances 0.000 description 2
- 238000009736 wetting Methods 0.000 description 2
- WHOZNOZYMBRCBL-OUKQBFOZSA-N (2E)-2-Tetradecenal Chemical compound CCCCCCCCCCC\C=C\C=O WHOZNOZYMBRCBL-OUKQBFOZSA-N 0.000 description 1
- RYAUSSKQMZRMAI-ALOPSCKCSA-N (2S,6R)-4-[3-(4-tert-butylphenyl)-2-methylpropyl]-2,6-dimethylmorpholine Chemical compound C=1C=C(C(C)(C)C)C=CC=1CC(C)CN1C[C@H](C)O[C@H](C)C1 RYAUSSKQMZRMAI-ALOPSCKCSA-N 0.000 description 1
- ALSTYHKOOCGGFT-KTKRTIGZSA-N (9Z)-octadecen-1-ol Chemical compound CCCCCCCC\C=C/CCCCCCCCO ALSTYHKOOCGGFT-KTKRTIGZSA-N 0.000 description 1
- ZORQXIQZAOLNGE-UHFFFAOYSA-N 1,1-difluorocyclohexane Chemical compound FC1(F)CCCCC1 ZORQXIQZAOLNGE-UHFFFAOYSA-N 0.000 description 1
- IIZPXYDJLKNOIY-JXPKJXOSSA-N 1-palmitoyl-2-arachidonoyl-sn-glycero-3-phosphocholine Chemical class CCCCCCCCCCCCCCCC(=O)OC[C@H](COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCC\C=C/C\C=C/C\C=C/C\C=C/CCCCC IIZPXYDJLKNOIY-JXPKJXOSSA-N 0.000 description 1
- PAWQVTBBRAZDMG-UHFFFAOYSA-N 2-(3-bromo-2-fluorophenyl)acetic acid Chemical compound OC(=O)CC1=CC=CC(Br)=C1F PAWQVTBBRAZDMG-UHFFFAOYSA-N 0.000 description 1
- NFAOATPOYUWEHM-UHFFFAOYSA-N 2-(6-methylheptyl)phenol Chemical class CC(C)CCCCCC1=CC=CC=C1O NFAOATPOYUWEHM-UHFFFAOYSA-N 0.000 description 1
- ZREHYDMEQQDRGS-UHFFFAOYSA-N 2-amino-2-ethyl-3-methylbutanoic acid Chemical compound CCC(N)(C(C)C)C(O)=O ZREHYDMEQQDRGS-UHFFFAOYSA-N 0.000 description 1
- OUCGJMIVSYHBEC-UHFFFAOYSA-N 2-ethylhexyl 2-ethylhexanoate Chemical compound CCCCC(CC)COC(=O)C(CC)CCCC OUCGJMIVSYHBEC-UHFFFAOYSA-N 0.000 description 1
- LWLRMRFJCCMNML-UHFFFAOYSA-N 2-ethylhexyl dodecanoate Chemical compound CCCCCCCCCCCC(=O)OCC(CC)CCCC LWLRMRFJCCMNML-UHFFFAOYSA-N 0.000 description 1
- SFAAOBGYWOUHLU-UHFFFAOYSA-N 2-ethylhexyl hexadecanoate Chemical compound CCCCCCCCCCCCCCCC(=O)OCC(CC)CCCC SFAAOBGYWOUHLU-UHFFFAOYSA-N 0.000 description 1
- DUIOKRXOKLLURE-UHFFFAOYSA-N 2-octylphenol Chemical compound CCCCCCCCC1=CC=CC=C1O DUIOKRXOKLLURE-UHFFFAOYSA-N 0.000 description 1
- FOGYNLXERPKEGN-UHFFFAOYSA-N 3-(2-hydroxy-3-methoxyphenyl)-2-[2-methoxy-4-(3-sulfopropyl)phenoxy]propane-1-sulfonic acid Chemical compound COC1=CC=CC(CC(CS(O)(=O)=O)OC=2C(=CC(CCCS(O)(=O)=O)=CC=2)OC)=C1O FOGYNLXERPKEGN-UHFFFAOYSA-N 0.000 description 1
- HIQIXEFWDLTDED-UHFFFAOYSA-N 4-hydroxy-1-piperidin-4-ylpyrrolidin-2-one Chemical compound O=C1CC(O)CN1C1CCNCC1 HIQIXEFWDLTDED-UHFFFAOYSA-N 0.000 description 1
- AMEMLELAMQEAIA-UHFFFAOYSA-N 6-(tert-butyl)thieno[3,2-d]pyrimidin-4(3H)-one Chemical compound N1C=NC(=O)C2=C1C=C(C(C)(C)C)S2 AMEMLELAMQEAIA-UHFFFAOYSA-N 0.000 description 1
- GPZYYYGYCRFPBU-UHFFFAOYSA-N 6-Hydroxyflavone Chemical compound C=1C(=O)C2=CC(O)=CC=C2OC=1C1=CC=CC=C1 GPZYYYGYCRFPBU-UHFFFAOYSA-N 0.000 description 1
- 235000019489 Almond oil Nutrition 0.000 description 1
- 241000283690 Bos taurus Species 0.000 description 1
- 239000007848 Bronsted acid Substances 0.000 description 1
- 235000017399 Caesalpinia tinctoria Nutrition 0.000 description 1
- 241000217446 Calystegia sepium Species 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- 240000006162 Chenopodium quinoa Species 0.000 description 1
- 244000060011 Cocos nucifera Species 0.000 description 1
- 235000013162 Cocos nucifera Nutrition 0.000 description 1
- XTJFFFGAUHQWII-UHFFFAOYSA-N Dibutyl adipate Chemical compound CCCCOC(=O)CCCCC(=O)OCCCC XTJFFFGAUHQWII-UHFFFAOYSA-N 0.000 description 1
- UDSFAEKRVUSQDD-UHFFFAOYSA-N Dimethyl adipate Chemical compound COC(=O)CCCCC(=O)OC UDSFAEKRVUSQDD-UHFFFAOYSA-N 0.000 description 1
- NEHDRDVHPTWWFG-UHFFFAOYSA-N Dioctyl hexanedioate Chemical compound CCCCCCCCOC(=O)CCCCC(=O)OCCCCCCCC NEHDRDVHPTWWFG-UHFFFAOYSA-N 0.000 description 1
- 229920005682 EO-PO block copolymer Polymers 0.000 description 1
- LVGKNOAMLMIIKO-UHFFFAOYSA-N Elaidinsaeure-aethylester Natural products CCCCCCCCC=CCCCCCCCC(=O)OCC LVGKNOAMLMIIKO-UHFFFAOYSA-N 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- 239000005778 Fenpropimorph Substances 0.000 description 1
- 235000010469 Glycine max Nutrition 0.000 description 1
- 238000003747 Grignard reaction Methods 0.000 description 1
- 244000020551 Helianthus annuus Species 0.000 description 1
- 235000003222 Helianthus annuus Nutrition 0.000 description 1
- NHTMVDHEPJAVLT-UHFFFAOYSA-N Isooctane Chemical compound CC(C)CC(C)(C)C NHTMVDHEPJAVLT-UHFFFAOYSA-N 0.000 description 1
- 239000002841 Lewis acid Substances 0.000 description 1
- 235000004431 Linum usitatissimum Nutrition 0.000 description 1
- 240000006240 Linum usitatissimum Species 0.000 description 1
- IGFHQQFPSIBGKE-UHFFFAOYSA-N Nonylphenol Natural products CCCCCCCCCC1=CC=C(O)C=C1 IGFHQQFPSIBGKE-UHFFFAOYSA-N 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 235000019483 Peanut oil Nutrition 0.000 description 1
- 229920001214 Polysorbate 60 Polymers 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- 108010009736 Protein Hydrolysates Proteins 0.000 description 1
- 235000019484 Rapeseed oil Nutrition 0.000 description 1
- 235000019485 Safflower oil Nutrition 0.000 description 1
- 229920002125 Sokalan® Polymers 0.000 description 1
- ULUAUXLGCMPNKK-UHFFFAOYSA-N Sulfobutanedioic acid Chemical class OC(=O)CC(C(O)=O)S(O)(=O)=O ULUAUXLGCMPNKK-UHFFFAOYSA-N 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 235000019486 Sunflower oil Nutrition 0.000 description 1
- 241000388430 Tara Species 0.000 description 1
- IJCWFDPJFXGQBN-RYNSOKOISA-N [(2R)-2-[(2R,3R,4S)-4-hydroxy-3-octadecanoyloxyoxolan-2-yl]-2-octadecanoyloxyethyl] octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OC[C@@H](OC(=O)CCCCCCCCCCCCCCCCC)[C@H]1OC[C@H](O)[C@H]1OC(=O)CCCCCCCCCCCCCCCCC IJCWFDPJFXGQBN-RYNSOKOISA-N 0.000 description 1
- 239000012190 activator Substances 0.000 description 1
- 150000001299 aldehydes Chemical class 0.000 description 1
- 238000005882 aldol condensation reaction Methods 0.000 description 1
- 150000007933 aliphatic carboxylic acids Chemical class 0.000 description 1
- 150000008044 alkali metal hydroxides Chemical class 0.000 description 1
- 150000001447 alkali salts Chemical class 0.000 description 1
- 229910001860 alkaline earth metal hydroxide Inorganic materials 0.000 description 1
- 125000003342 alkenyl group Chemical group 0.000 description 1
- 150000003973 alkyl amines Chemical class 0.000 description 1
- 150000008055 alkyl aryl sulfonates Chemical class 0.000 description 1
- 229940045714 alkyl sulfonate alkylating agent Drugs 0.000 description 1
- 150000008052 alkyl sulfonates Chemical class 0.000 description 1
- 239000008168 almond oil Substances 0.000 description 1
- 150000001413 amino acids Chemical class 0.000 description 1
- 150000003868 ammonium compounds Chemical class 0.000 description 1
- BFNBIHQBYMNNAN-UHFFFAOYSA-N ammonium sulfate Chemical compound N.N.OS(O)(=O)=O BFNBIHQBYMNNAN-UHFFFAOYSA-N 0.000 description 1
- 229910052921 ammonium sulfate Inorganic materials 0.000 description 1
- 235000011130 ammonium sulphate Nutrition 0.000 description 1
- 239000010775 animal oil Substances 0.000 description 1
- 230000008485 antagonism Effects 0.000 description 1
- 239000007900 aqueous suspension Substances 0.000 description 1
- 150000001491 aromatic compounds Chemical class 0.000 description 1
- 238000010923 batch production Methods 0.000 description 1
- 235000012216 bentonite Nutrition 0.000 description 1
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical class OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 1
- 230000003115 biocidal effect Effects 0.000 description 1
- 230000004071 biological effect Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- SAOKZLXYCUGLFA-UHFFFAOYSA-N bis(2-ethylhexyl) adipate Chemical compound CCCCC(CC)COC(=O)CCCCC(=O)OCC(CC)CCCC SAOKZLXYCUGLFA-UHFFFAOYSA-N 0.000 description 1
- MQKXWEJVDDRQKK-UHFFFAOYSA-N bis(6-methylheptyl) butanedioate Chemical compound CC(C)CCCCCOC(=O)CCC(=O)OCCCCCC(C)C MQKXWEJVDDRQKK-UHFFFAOYSA-N 0.000 description 1
- CJFLBOQMPJCWLR-UHFFFAOYSA-N bis(6-methylheptyl) hexanedioate Chemical compound CC(C)CCCCCOC(=O)CCCCC(=O)OCCCCCC(C)C CJFLBOQMPJCWLR-UHFFFAOYSA-N 0.000 description 1
- HORIEOQXBKUKGQ-UHFFFAOYSA-N bis(7-methyloctyl) cyclohexane-1,2-dicarboxylate Chemical compound CC(C)CCCCCCOC(=O)C1CCCCC1C(=O)OCCCCCCC(C)C HORIEOQXBKUKGQ-UHFFFAOYSA-N 0.000 description 1
- 229920001400 block copolymer Polymers 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 150000007942 carboxylates Chemical class 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 239000006184 cosolvent Substances 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- HPXRVTGHNJAIIH-UHFFFAOYSA-N cyclohexanol Chemical compound OC1CCCCC1 HPXRVTGHNJAIIH-UHFFFAOYSA-N 0.000 description 1
- 239000003599 detergent Substances 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- GDVKFRBCXAPAQJ-UHFFFAOYSA-A dialuminum;hexamagnesium;carbonate;hexadecahydroxide Chemical compound [OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Al+3].[Al+3].[O-]C([O-])=O GDVKFRBCXAPAQJ-UHFFFAOYSA-A 0.000 description 1
- 150000001990 dicarboxylic acid derivatives Chemical class 0.000 description 1
- 239000002283 diesel fuel Substances 0.000 description 1
- 238000007865 diluting Methods 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 238000006471 dimerization reaction Methods 0.000 description 1
- JVSWJIKNEAIKJW-UHFFFAOYSA-N dimethyl-hexane Natural products CCCCCC(C)C JVSWJIKNEAIKJW-UHFFFAOYSA-N 0.000 description 1
- KWABLUYIOFEZOY-UHFFFAOYSA-N dioctyl butanedioate Chemical compound CCCCCCCCOC(=O)CCC(=O)OCCCCCCCC KWABLUYIOFEZOY-UHFFFAOYSA-N 0.000 description 1
- XPPKVPWEQAFLFU-UHFFFAOYSA-N diphosphoric acid Chemical compound OP(O)(=O)OP(O)(O)=O XPPKVPWEQAFLFU-UHFFFAOYSA-N 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- LZJUZSYHFSVIGJ-UHFFFAOYSA-N ditridecyl hexanedioate Chemical compound CCCCCCCCCCCCCOC(=O)CCCCC(=O)OCCCCCCCCCCCCC LZJUZSYHFSVIGJ-UHFFFAOYSA-N 0.000 description 1
- LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 description 1
- YRIUSKIDOIARQF-UHFFFAOYSA-N dodecyl benzenesulfonate Chemical class CCCCCCCCCCCCOS(=O)(=O)C1=CC=CC=C1 YRIUSKIDOIARQF-UHFFFAOYSA-N 0.000 description 1
- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- QYDYPVFESGNLHU-UHFFFAOYSA-N elaidic acid methyl ester Natural products CCCCCCCCC=CCCCCCCCC(=O)OC QYDYPVFESGNLHU-UHFFFAOYSA-N 0.000 description 1
- 239000012167 epicuticular wax Substances 0.000 description 1
- 125000004494 ethyl ester group Chemical group 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- LVGKNOAMLMIIKO-QXMHVHEDSA-N ethyl oleate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OCC LVGKNOAMLMIIKO-QXMHVHEDSA-N 0.000 description 1
- 229940093471 ethyl oleate Drugs 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 150000002191 fatty alcohols Chemical class 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- YQEMORVAKMFKLG-UHFFFAOYSA-N glycerine monostearate Natural products CCCCCCCCCCCCCCCCCC(=O)OC(CO)CO YQEMORVAKMFKLG-UHFFFAOYSA-N 0.000 description 1
- SVUQHVRAGMNPLW-UHFFFAOYSA-N glycerol monostearate Natural products CCCCCCCCCCCCCCCCC(=O)OCC(O)CO SVUQHVRAGMNPLW-UHFFFAOYSA-N 0.000 description 1
- 150000002314 glycerols Chemical class 0.000 description 1
- 125000005842 heteroatom Chemical group 0.000 description 1
- 239000008240 homogeneous mixture Substances 0.000 description 1
- 239000003864 humus Substances 0.000 description 1
- 125000001165 hydrophobic group Chemical group 0.000 description 1
- 229910001701 hydrotalcite Inorganic materials 0.000 description 1
- 229960001545 hydrotalcite Drugs 0.000 description 1
- 150000002462 imidazolines Chemical class 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 238000009776 industrial production Methods 0.000 description 1
- 239000011261 inert gas Substances 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- VQTUBCCKSQIDNK-UHFFFAOYSA-N iso-butene Natural products CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 description 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 229940033357 isopropyl laurate Drugs 0.000 description 1
- 229940074928 isopropyl myristate Drugs 0.000 description 1
- 239000003350 kerosene Substances 0.000 description 1
- 229940071085 lauroyl glutamate Drugs 0.000 description 1
- 239000010985 leather Substances 0.000 description 1
- 229940067606 lecithin Drugs 0.000 description 1
- 150000007517 lewis acids Chemical class 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 229940057995 liquid paraffin Drugs 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- QYDYPVFESGNLHU-KHPPLWFESA-N methyl oleate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OC QYDYPVFESGNLHU-KHPPLWFESA-N 0.000 description 1
- 229940073769 methyl oleate Drugs 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 235000010981 methylcellulose Nutrition 0.000 description 1
- 238000007431 microscopic evaluation Methods 0.000 description 1
- ONHFWHCMZAJCFB-UHFFFAOYSA-N myristamine oxide Chemical compound CCCCCCCCCCCCCC[N+](C)(C)[O-] ONHFWHCMZAJCFB-UHFFFAOYSA-N 0.000 description 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000001280 n-hexyl group Chemical group C(CCCCC)* 0.000 description 1
- 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 239000012454 non-polar solvent Substances 0.000 description 1
- 231100001184 nonphytotoxic Toxicity 0.000 description 1
- SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical compound CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 1
- 235000018343 nutrient deficiency Nutrition 0.000 description 1
- 229940038384 octadecane Drugs 0.000 description 1
- BBZAGOMQOSEWBH-UHFFFAOYSA-N octyl dodecanoate Chemical compound CCCCCCCCCCCC(=O)OCCCCCCCC BBZAGOMQOSEWBH-UHFFFAOYSA-N 0.000 description 1
- 239000012053 oil suspension Substances 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid group Chemical group C(CCCCCCC\C=C/CCCCCCCC)(=O)O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- 229940055577 oleyl alcohol Drugs 0.000 description 1
- XMLQWXUVTXCDDL-UHFFFAOYSA-N oleyl alcohol Natural products CCCCCCC=CCCCCCCCCCCO XMLQWXUVTXCDDL-UHFFFAOYSA-N 0.000 description 1
- 239000004006 olive oil Substances 0.000 description 1
- 235000008390 olive oil Nutrition 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- IPCSVZSSVZVIGE-UHFFFAOYSA-N palmitic acid group Chemical group C(CCCCCCCCCCCCCCC)(=O)O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 1
- 239000010690 paraffinic oil Substances 0.000 description 1
- 239000000312 peanut oil Substances 0.000 description 1
- 229940083254 peripheral vasodilators imidazoline derivative Drugs 0.000 description 1
- 230000002572 peristaltic effect Effects 0.000 description 1
- 239000008194 pharmaceutical composition Substances 0.000 description 1
- 229940044654 phenolsulfonic acid Drugs 0.000 description 1
- 235000021317 phosphate Nutrition 0.000 description 1
- 150000003904 phospholipids Chemical class 0.000 description 1
- PJGSXYOJTGTZAV-UHFFFAOYSA-N pinacolone Chemical compound CC(=O)C(C)(C)C PJGSXYOJTGTZAV-UHFFFAOYSA-N 0.000 description 1
- 230000008635 plant growth Effects 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 230000010152 pollination Effects 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 1
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
- 229940114930 potassium stearate Drugs 0.000 description 1
- ANBFRLKBEIFNQU-UHFFFAOYSA-M potassium;octadecanoate Chemical compound [K+].CCCCCCCCCCCCCCCCCC([O-])=O ANBFRLKBEIFNQU-UHFFFAOYSA-M 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 150000003138 primary alcohols Chemical class 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- 239000003531 protein hydrolysate Substances 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 238000010188 recombinant method Methods 0.000 description 1
- 235000005713 safflower oil Nutrition 0.000 description 1
- 239000003813 safflower oil Substances 0.000 description 1
- 239000012266 salt solution Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 108700004121 sarkosyl Proteins 0.000 description 1
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 238000004062 sedimentation Methods 0.000 description 1
- 239000008159 sesame oil Substances 0.000 description 1
- 235000011803 sesame oil Nutrition 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 239000012748 slip agent Substances 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- KSAVQLQVUXSOCR-UHFFFAOYSA-M sodium lauroyl sarcosinate Chemical compound [Na+].CCCCCCCCCCCC(=O)N(C)CC([O-])=O KSAVQLQVUXSOCR-UHFFFAOYSA-M 0.000 description 1
- 229940045885 sodium lauroyl sarcosinate Drugs 0.000 description 1
- 239000001593 sorbitan monooleate Substances 0.000 description 1
- 235000011069 sorbitan monooleate Nutrition 0.000 description 1
- 229940035049 sorbitan monooleate Drugs 0.000 description 1
- 239000001589 sorbitan tristearate Substances 0.000 description 1
- 235000011078 sorbitan tristearate Nutrition 0.000 description 1
- 229960004129 sorbitan tristearate Drugs 0.000 description 1
- 239000003549 soybean oil Substances 0.000 description 1
- 235000012424 soybean oil Nutrition 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 230000006641 stabilisation Effects 0.000 description 1
- 238000011105 stabilization Methods 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 150000003460 sulfonic acids Chemical class 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000002600 sunflower oil Substances 0.000 description 1
- 238000013268 sustained release Methods 0.000 description 1
- 239000012730 sustained-release form Substances 0.000 description 1
- 239000002641 tar oil Substances 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 125000005329 tetralinyl group Chemical class C1(CCCC2=CC=CC=C12)* 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 150000003568 thioethers Chemical class 0.000 description 1
- 231100000027 toxicology Toxicity 0.000 description 1
- 235000013619 trace mineral Nutrition 0.000 description 1
- 239000011573 trace mineral Substances 0.000 description 1
- 150000003626 triacylglycerols Chemical class 0.000 description 1
- 229940099259 vaseline Drugs 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 235000019871 vegetable fat Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 239000002351 wastewater Substances 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
- A01N25/30—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 characterised by the surfactants
-
- 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
- A01N31/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic oxygen or sulfur compounds
- A01N31/02—Acyclic compounds
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Environmental Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (AREA)
- Zoology (AREA)
- Plant Pathology (AREA)
- Toxicology (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Emulsifying, Dispersing, Foam-Producing Or Wetting Agents (AREA)
- Cultivation Of Plants (AREA)
- Fertilizers (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE10218316 | 2002-04-24 | ||
| PCT/EP2003/004276 WO2003090531A1 (de) | 2002-04-24 | 2003-04-24 | Verwendung bestimmter alkoholalkoxylate als adjuvans für den agrotechnischen bereich |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| EA200401383A1 EA200401383A1 (ru) | 2005-04-28 |
| EA011649B1 true EA011649B1 (ru) | 2009-04-28 |
Family
ID=29264806
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EA200401383A EA011649B1 (ru) | 2002-04-24 | 2003-04-24 | Композиция на основе алкоксилатов спиртов и их применение в качестве адъюванта в области агротехники |
| EA200900076A EA015423B1 (ru) | 2002-04-24 | 2003-04-24 | Применение определенных алкоксилатов спиртов в качестве адъюванта в области агротехники |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EA200900076A EA015423B1 (ru) | 2002-04-24 | 2003-04-24 | Применение определенных алкоксилатов спиртов в качестве адъюванта в области агротехники |
Country Status (24)
| Country | Link |
|---|---|
| US (2) | US8129312B2 (https=) |
| EP (2) | EP1501355B1 (https=) |
| JP (1) | JP4417118B2 (https=) |
| KR (1) | KR100983437B1 (https=) |
| CN (1) | CN100370900C (https=) |
| AT (1) | ATE468016T1 (https=) |
| AU (2) | AU2003232505B2 (https=) |
| BR (2) | BR122013024224B1 (https=) |
| CA (2) | CA2697544C (https=) |
| CY (1) | CY1110732T1 (https=) |
| DE (1) | DE50312724D1 (https=) |
| DK (1) | DK1501355T3 (https=) |
| EA (2) | EA011649B1 (https=) |
| ES (1) | ES2345980T3 (https=) |
| IL (2) | IL164524A (https=) |
| IN (1) | IN2004CH02386A (https=) |
| MX (1) | MXPA04010344A (https=) |
| NZ (1) | NZ536029A (https=) |
| PL (2) | PL211208B1 (https=) |
| PT (1) | PT1501355E (https=) |
| SI (1) | SI1501355T1 (https=) |
| UA (1) | UA82192C2 (https=) |
| WO (1) | WO2003090531A1 (https=) |
| ZA (1) | ZA200409411B (https=) |
Families Citing this family (44)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20090023820A1 (en) * | 2006-02-22 | 2009-01-22 | Basf Se | Surfactant mixture containing short-chain and also long-chain components |
| UA89599C2 (uk) * | 2006-08-04 | 2010-02-10 | Басф Се | Водний концентрат діючої речовини з гербіцидною дією та спосіб боротьби з небажаним ростом рослин |
| JP5266247B2 (ja) * | 2006-12-07 | 2013-08-21 | ビーエーエスエフ ソシエタス・ヨーロピア | 殺菌性トリアゾールおよびアルコキシル化アルコールを含む組成物およびキットならびにそれらの使用 |
| CA2683034A1 (en) * | 2007-04-25 | 2008-11-06 | Michael Stoesser | Alcohol alkoxylates, compositions containing these, and use of the alcohol alkoxylates as adjuvants for the agrochemical field |
| ES2323399B2 (es) * | 2007-06-19 | 2010-02-26 | Gat Microencapsulation Ag | Suspensiones en aceites de sulfonilureas y combinaciones agroquimicas. |
| CN101848639A (zh) * | 2007-07-20 | 2010-09-29 | 巴斯夫欧洲公司 | 含有醇烷氧基化物的组合物以及醇烷氧基化物在农业化学领域作为辅助剂的用途 |
| US20120021914A1 (en) * | 2008-04-24 | 2012-01-26 | Basf Se | Cyclodextrin-containing suspension concentrates, method for producing the same and their use |
| WO2009130281A1 (de) | 2008-04-24 | 2009-10-29 | Basf Se | Alkoholalkoxylate, diese enthaltende mittel und verwendung der alkoholalkoxylate als adjuvans für den agrochemischen bereich |
| EP2147599A1 (en) * | 2008-07-23 | 2010-01-27 | Cognis IP Management GmbH | Agricultural compositions |
| JP5606442B2 (ja) | 2008-09-26 | 2014-10-15 | ビーエーエスエフ ソシエタス・ヨーロピア | 水に乳化可能な液体活性成分濃縮液 |
| DE102008043185A1 (de) * | 2008-10-27 | 2010-04-29 | Evonik Goldschmidt Gmbh | Nicht schäumende organische Tenside als Additive für Tankmischungszubereitungen im Pflanzenschutz |
| FR2949643B1 (fr) * | 2009-09-08 | 2012-09-28 | Fonds De Dev Des Filieres Des Oleagineux Et Proteagineux Fidop | Utilisation d'ethers de glycerol comme activateurs des effets herbicides d'une substance herbicide |
| EP2305030A1 (de) | 2009-09-14 | 2011-04-06 | Bayer CropScience AG | Alkylpolypropylenglycolpolyethylenglycol enthaltende agrochemische Zusammensetzungen |
| KR20130039331A (ko) * | 2010-06-29 | 2013-04-19 | 바이엘 인텔렉쳐 프로퍼티 게엠베하 | 사이클릭 카보닐아미딘을 포함하는 개량된 살충성 조성물 |
| EP2457890A1 (en) | 2010-11-29 | 2012-05-30 | Cognis IP Management GmbH | Biocide compositions comprising alkoxylation products of isoamyl alcohol derivatives |
| CA2827508A1 (en) * | 2011-02-16 | 2013-07-18 | Fashion Chemicals, Gmbh & Co Kg | Alkoxylated non-ionic alkanol adjuvant formulations and methods for making and using the same |
| TWI634840B (zh) * | 2011-03-31 | 2018-09-11 | 先正達合夥公司 | 植物生長調節組成物及使用其之方法 |
| ES2756799T3 (es) | 2011-04-20 | 2020-04-27 | Huntsman Petrochemical Llc | Uso de agentes de reducción de deriva de la pulverización que comprenden tensioactivos de bajo equilibrio hidrófilo-lipófilo |
| EP2811828B1 (en) * | 2012-01-23 | 2021-09-01 | Syngenta Participations AG | Adjuvant compositions |
| ES2824106T3 (es) * | 2012-04-24 | 2021-05-11 | Stepan Co | Alcoxilatos de alcoholes grasos insaturados a partir de la metátesis de aceites naturales |
| SG11201406858WA (en) | 2012-04-24 | 2014-11-27 | Stepan Co | Unsaturated fatty alcohol derivatives from natural oil metathesis |
| US9591854B2 (en) | 2012-06-18 | 2017-03-14 | Basf Se | Agroformulations containing a lactone based alkoxylate |
| BR112015005605A2 (pt) * | 2012-09-13 | 2017-08-08 | Rhodia Operations | musgo de turfa com capacidade de umedecimento, método de preparação, e método de utilização |
| CN104704100B (zh) * | 2012-09-29 | 2018-12-25 | 陶氏环球技术有限责任公司 | 烷氧基化物组合物和其作为农业佐剂的用途 |
| JP6396315B2 (ja) * | 2012-12-14 | 2018-09-26 | ビーエイエスエフ・ソシエタス・エウロパエアＢａｓｆ Ｓｅ | 農薬および２―イソプロピル―５―メチルヘキサン―１―アミンのアルコキシレートを含む組成物 |
| AU2015213032B2 (en) * | 2014-01-30 | 2018-11-01 | Basf Se | Asymmetric formales and acetales as adjuvants for crop protection |
| CN106455555B (zh) | 2014-05-06 | 2021-03-12 | 巴斯夫欧洲公司 | 包含农药和羟烷基聚氧化烯二醇醚的组合物 |
| MX382072B (es) * | 2014-06-06 | 2025-03-12 | Archer Daniels Midland Co | Microemulsiones y sus usos. |
| UA118991C2 (uk) * | 2014-09-16 | 2019-04-10 | Басф Се | Агрохімічний суспензійний концентрат, що включає алкоксильований спирт, розчинений у водній фазі |
| CA2975025A1 (en) | 2015-02-10 | 2016-08-18 | Basf Se | Composition comprising a pesticide and an alkoxylated ester |
| PL3636691T3 (pl) | 2015-10-07 | 2021-09-27 | Elementis Specialties, Inc. | Środek zwilżający i przeciwpieniący |
| US10590010B2 (en) | 2015-11-06 | 2020-03-17 | Solenis Technologies, L.P. | Processes for the separation of water from aqueous systems |
| CA3006787A1 (en) * | 2015-12-09 | 2017-06-15 | Akzo Nobel Chemicals International B.V. | Low foaming high electrolyte compositions |
| AU2018214226B2 (en) | 2017-02-03 | 2023-07-13 | Grains Research And Development Corporation (Grdc) | Methods to enhance soil water infiltration and to reduce soil water repellency using a surfactant composition |
| EP3622028B1 (en) | 2017-05-10 | 2022-09-07 | Basf Se | Polymer with branched structure |
| IL273412B (en) * | 2017-09-20 | 2022-09-01 | Basf Se | Treated medium for plant growth that has increased water retention |
| WO2019185610A1 (en) | 2018-03-26 | 2019-10-03 | Basf Se | Method of reducing soil water repellency |
| WO2019185612A1 (en) | 2018-03-26 | 2019-10-03 | Basf Se | Method of reducing soil water repellency |
| UA128582C2 (uk) * | 2018-07-30 | 2024-08-21 | Байєр Акцієнгезелльшафт | Гербіцидні композиції з поліпшеними властивостями |
| US20220015356A1 (en) * | 2018-12-11 | 2022-01-20 | Dow Global Technologies Llc | Aqueous solutions of poorly soluble pesticides using polyalkyoxylated alcohols |
| EP3996504A1 (en) * | 2019-07-11 | 2022-05-18 | Basf Se | Shear stable composition for spray drift control |
| CA3253001A1 (en) * | 2022-05-11 | 2023-11-16 | Adama Makhteshim Ltd. | PHTALIMIDE FUNGICIDE COMPOSITION |
| EP4338592A1 (en) | 2022-09-15 | 2024-03-20 | Basf Se | Use of compound for improving the efficacy of herbicides |
| WO2024140689A1 (en) * | 2022-12-29 | 2024-07-04 | Momentive Performance Materials Inc. | Adjuvant compositions and method for treating plant using the same |
Citations (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0473003A2 (de) * | 1990-08-24 | 1992-03-04 | Bayer Ag | Feststoff-Formulierungen |
| WO1995018531A1 (en) * | 1994-01-10 | 1995-07-13 | Ciba-Geigy Ag | Wettable powder formulations of herbicides |
| WO1996031121A1 (en) * | 1995-04-06 | 1996-10-10 | Nippon Soda Co., Ltd. | Herbicidal composition |
| WO1997000010A1 (en) * | 1995-06-16 | 1997-01-03 | Monsanto Company | Surfactants providing enhanced efficacy and/or rainfastness to pesticide formulations |
| US5661121A (en) * | 1992-11-19 | 1997-08-26 | Berol Nobel Ab | 2-propyl heptanol alkoxylates and process of cleaning hard surfaces therewith |
| WO1999003345A1 (en) * | 1997-07-15 | 1999-01-28 | Kao Corporation | Effect enhancer for agricultural chemical |
| US6057284A (en) * | 1996-05-30 | 2000-05-02 | Basf Aktiengesellschaft | Iso-tridecanolalkoxylates in block form as low-foam or antifoaming surfactants |
| US6124301A (en) * | 1998-03-17 | 2000-09-26 | American Cyanamid Company | Enhancement of the efficacy of triazolopyrimidines |
| WO2001030147A1 (fr) * | 1999-10-29 | 2001-05-03 | Aventis Cropscience Sa | Nouvelles compositions pesticides et/ou regulatrices de croissance a agent tensio-actif non ionique particulier |
| WO2001077276A1 (de) * | 2000-04-07 | 2001-10-18 | Basf Aktiengesellschaft | Alkoholalkoxylate als schaumarme oder schaumdämpfende tenside |
Family Cites Families (20)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4966728A (en) | 1988-08-26 | 1990-10-30 | Basf Corporation | Adjuvants for use with postemergent herbicides |
| IL91418A (en) | 1988-09-01 | 1997-11-20 | Rhone Poulenc Agrochimie | (hetero) cyclic amide derivatives, process for their preparation and fungicidal compositions containing them |
| US5230892A (en) | 1990-08-24 | 1993-07-27 | Bayer Aktiengesellschaft | Solid formulations |
| FR2685328B1 (fr) | 1991-12-20 | 1995-12-01 | Rhone Poulenc Agrochimie | Derives de 2-imidazoline-5-ones et 2-imidazoline-5-thiones fongicides. |
| FR2706456B1 (fr) | 1993-06-18 | 1996-06-28 | Rhone Poulenc Agrochimie | Dérivés optiquement actifs de 2-imidazoline-5-ones et 2-imidazoline-5-thiones fongicides. |
| FR2694288B1 (fr) | 1992-06-30 | 1994-09-09 | Rhone Poulenc Agrochimie | Phenylbenzamides fongicides et procédés pour les préparer. |
| CA2093377A1 (en) | 1993-04-05 | 1994-10-06 | David Gilbert Chasin | Solid agricultural adjuvants |
| DE4339713A1 (de) | 1993-11-22 | 1995-05-24 | Basf Ag | Verfahren zur Oligomerisierung von Olefinen zu hochlinearen Oligomeren und Katalysatoren dafür |
| DE4416303A1 (de) | 1994-05-09 | 1995-11-16 | Bayer Ag | Schaumarmes Netzmittel und seine Verwendung |
| GB9703054D0 (en) | 1997-02-14 | 1997-04-02 | Ici Plc | Agrochemical surfactant compositions |
| GB9718139D0 (en) * | 1997-08-27 | 1997-10-29 | Zeneca Ltd | Agrochemical Formulation |
| DE19857963A1 (de) * | 1998-12-16 | 2000-06-21 | Bayer Ag | Agrochemische Formulierungen |
| US6235300B1 (en) * | 1999-01-19 | 2001-05-22 | Amway Corporation | Plant protecting adjuvant containing topped or peaked alcohol alkoxylates and conventional alcohol alkoxylates |
| DE10029169A1 (de) | 2000-06-19 | 2002-01-03 | Aventis Cropscience Gmbh | Herbizide Mittel |
| ES2223932T3 (es) | 2000-08-25 | 2005-03-01 | Basf Aktiengesellschaft | Formulacion fungicida. |
| US6479449B1 (en) * | 2002-04-19 | 2002-11-12 | Colgate-Palmolive Company | Cleaning system including a liquid cleaning composition disposed in a water soluble container |
| US20080064756A1 (en) | 2003-08-14 | 2008-03-13 | Basf Aktiengesellschaft | Use of Alcohol-Oxyalkylates in the Form of Adjuvants for Benzamidoxime Fungicidal Derivatives, Appropriate Agents and Kits |
| CA2683034A1 (en) | 2007-04-25 | 2008-11-06 | Michael Stoesser | Alcohol alkoxylates, compositions containing these, and use of the alcohol alkoxylates as adjuvants for the agrochemical field |
| CN101848639A (zh) | 2007-07-20 | 2010-09-29 | 巴斯夫欧洲公司 | 含有醇烷氧基化物的组合物以及醇烷氧基化物在农业化学领域作为辅助剂的用途 |
| WO2009130281A1 (de) | 2008-04-24 | 2009-10-29 | Basf Se | Alkoholalkoxylate, diese enthaltende mittel und verwendung der alkoholalkoxylate als adjuvans für den agrochemischen bereich |
-
2003
- 2003-04-24 JP JP2003587180A patent/JP4417118B2/ja not_active Expired - Lifetime
- 2003-04-24 BR BRBR122013024224-4A patent/BR122013024224B1/pt not_active IP Right Cessation
- 2003-04-24 PL PL373335A patent/PL211208B1/pl unknown
- 2003-04-24 DE DE50312724T patent/DE50312724D1/de not_active Expired - Lifetime
- 2003-04-24 CA CA2697544A patent/CA2697544C/en not_active Expired - Fee Related
- 2003-04-24 BR BRPI0309492-8A patent/BR0309492B1/pt active IP Right Grant
- 2003-04-24 PT PT03747121T patent/PT1501355E/pt unknown
- 2003-04-24 CN CNB038118548A patent/CN100370900C/zh not_active Expired - Lifetime
- 2003-04-24 MX MXPA04010344A patent/MXPA04010344A/es active IP Right Grant
- 2003-04-24 US US10/512,422 patent/US8129312B2/en active Active
- 2003-04-24 PL PL390684A patent/PL211842B1/pl unknown
- 2003-04-24 EP EP03747121A patent/EP1501355B1/de not_active Expired - Lifetime
- 2003-04-24 EA EA200401383A patent/EA011649B1/ru not_active IP Right Cessation
- 2003-04-24 KR KR1020047017042A patent/KR100983437B1/ko not_active Expired - Fee Related
- 2003-04-24 DK DK03747121.6T patent/DK1501355T3/da active
- 2003-04-24 SI SI200331846T patent/SI1501355T1/sl unknown
- 2003-04-24 ES ES03747121T patent/ES2345980T3/es not_active Expired - Lifetime
- 2003-04-24 AU AU2003232505A patent/AU2003232505B2/en not_active Expired
- 2003-04-24 CA CA2482758A patent/CA2482758C/en not_active Expired - Lifetime
- 2003-04-24 AT AT03747121T patent/ATE468016T1/de active
- 2003-04-24 NZ NZ536029A patent/NZ536029A/en not_active IP Right Cessation
- 2003-04-24 WO PCT/EP2003/004276 patent/WO2003090531A1/de not_active Ceased
- 2003-04-24 EP EP09181019.2A patent/EP2181593B2/de not_active Expired - Lifetime
- 2003-04-24 EA EA200900076A patent/EA015423B1/ru not_active IP Right Cessation
- 2003-04-24 UA UA20041109629A patent/UA82192C2/uk unknown
-
2004
- 2004-10-12 IL IL164524A patent/IL164524A/en active IP Right Grant
- 2004-10-20 IN IN2386CH2004 patent/IN2004CH02386A/en unknown
- 2004-11-23 ZA ZA200409411A patent/ZA200409411B/en unknown
-
2009
- 2009-05-26 IL IL198972A patent/IL198972A/en active IP Right Grant
- 2009-11-25 AU AU2009240808A patent/AU2009240808B2/en not_active Ceased
-
2010
- 2010-08-11 CY CY20101100752T patent/CY1110732T1/el unknown
-
2012
- 2012-02-03 US US13/365,958 patent/US8877681B2/en not_active Expired - Fee Related
Patent Citations (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0473003A2 (de) * | 1990-08-24 | 1992-03-04 | Bayer Ag | Feststoff-Formulierungen |
| US5661121A (en) * | 1992-11-19 | 1997-08-26 | Berol Nobel Ab | 2-propyl heptanol alkoxylates and process of cleaning hard surfaces therewith |
| WO1995018531A1 (en) * | 1994-01-10 | 1995-07-13 | Ciba-Geigy Ag | Wettable powder formulations of herbicides |
| WO1996031121A1 (en) * | 1995-04-06 | 1996-10-10 | Nippon Soda Co., Ltd. | Herbicidal composition |
| WO1997000010A1 (en) * | 1995-06-16 | 1997-01-03 | Monsanto Company | Surfactants providing enhanced efficacy and/or rainfastness to pesticide formulations |
| US6057284A (en) * | 1996-05-30 | 2000-05-02 | Basf Aktiengesellschaft | Iso-tridecanolalkoxylates in block form as low-foam or antifoaming surfactants |
| WO1999003345A1 (en) * | 1997-07-15 | 1999-01-28 | Kao Corporation | Effect enhancer for agricultural chemical |
| US6124301A (en) * | 1998-03-17 | 2000-09-26 | American Cyanamid Company | Enhancement of the efficacy of triazolopyrimidines |
| WO2001030147A1 (fr) * | 1999-10-29 | 2001-05-03 | Aventis Cropscience Sa | Nouvelles compositions pesticides et/ou regulatrices de croissance a agent tensio-actif non ionique particulier |
| WO2001077276A1 (de) * | 2000-04-07 | 2001-10-18 | Basf Aktiengesellschaft | Alkoholalkoxylate als schaumarme oder schaumdämpfende tenside |
Also Published As
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| EA011649B1 (ru) | Композиция на основе алкоксилатов спиртов и их применение в качестве адъюванта в области агротехники | |
| US5741502A (en) | Homogeneous, essentially nonaqueous adjuvant compositions with buffering capability | |
| EP2317846B1 (en) | Surfactant blends useful in agriculture | |
| AU2009248053B2 (en) | Pesticidal compositions | |
| RU2704450C2 (ru) | Композиция, содержащая пестицид и гидроксиалкиловый простой эфир полиоксиленгликоля | |
| JP2020128374A (ja) | 作物保護用アジュバントとしてのアルコールアルコキシレートカーボネート | |
| RU2241699C2 (ru) | Способ получения поверхностно-активного вещества, композиция на его основе, пестицидная композиция и способ защиты сельскохозяйственных культур | |
| EP2877563A1 (en) | Alkoxylate compositions and their use as agricultural adjuvants | |
| US6753003B1 (en) | Dithiocarbamate liquid formulations | |
| WO2002021921A1 (de) | Öl-suspensionskonzentrate auf basis eines cyclohexenonoximether-lithiumsalzes und deren verwendung als pflanzenschutzmittel | |
| KR20180095871A (ko) | 덴드리머 및 그의 배합물 | |
| PL210034B1 (pl) | Środek do stosowania w uprawie roślin i jego zastosowanie | |
| US6764979B2 (en) | Aqueous herbicidal agent | |
| JP4256161B2 (ja) | 均質相に基づく組成物、及び硝酸アンモニウムによるその安定化、ならびに、生物調節剤としての該組成物の使用 | |
| CA2333163A1 (en) | Aqueous, agrochemical agents containing active ingredients | |
| JP3597470B2 (ja) | 成長抑制水性組成物 | |
| CN102014629A (zh) | 除草剂混合物 | |
| USRE37313E1 (en) | Homogeneous, essentially nonaqueous adjuvant compositions with buffering capability | |
| JP2002522400A (ja) | アルコキシル化アミンで中和された芳香族スルホン酸界面活性剤を含有する農薬製剤 | |
| EP1942729A1 (de) | Polyalkoxylat-haltige feststoffformulierungen, verfahren zu ihrer herstellung und ihre verwendung | |
| CN104507307A (zh) | 包括醚-酰胺化合物的植物检疫组合物 | |
| RU2713793C2 (ru) | Композиция, содержащая пестицид и алкоксилированный сложный эфир | |
| CN109362753A (zh) | 一种含有甲氨基阿维菌素苯甲酸盐的杀虫组合物 | |
| KR101146500B1 (ko) | 제초제 조성물 | |
| BR112015013713B1 (pt) | composição, método de preparação da composição, alcoxilato e método para o controle dos fungos fitopatogênicos |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| MM4A | Lapse of a eurasian patent due to non-payment of renewal fees within the time limit in the following designated state(s) |
Designated state(s): AM AZ BY KZ KG MD TJ TM |