PH26428A - Adjuvants for use with postemergent herbicides - Google Patents
Adjuvants for use with postemergent herbicides Download PDFInfo
- Publication number
- PH26428A PH26428A PH39121A PH39121A PH26428A PH 26428 A PH26428 A PH 26428A PH 39121 A PH39121 A PH 39121A PH 39121 A PH39121 A PH 39121A PH 26428 A PH26428 A PH 26428A
- Authority
- PH
- Philippines
- Prior art keywords
- percent
- component
- adjuvant
- group
- weight
- Prior art date
Links
- 239000002671 adjuvant Substances 0.000 title claims description 39
- 239000004009 herbicide Substances 0.000 title claims description 37
- 239000004094 surface-active agent Substances 0.000 claims description 34
- 239000000203 mixture Substances 0.000 claims description 30
- 238000005187 foaming Methods 0.000 claims description 25
- -1 polyoxy Polymers 0.000 claims description 25
- 229930195733 hydrocarbon Natural products 0.000 claims description 19
- 150000002430 hydrocarbons Chemical class 0.000 claims description 19
- 150000002148 esters Chemical class 0.000 claims description 18
- 230000002363 herbicidal effect Effects 0.000 claims description 17
- 239000004215 Carbon black (E152) Substances 0.000 claims description 16
- 125000004432 carbon atom Chemical group C* 0.000 claims description 15
- 125000002947 alkylene group Chemical group 0.000 claims description 14
- 239000002904 solvent Substances 0.000 claims description 14
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims description 12
- 229920000570 polyether Polymers 0.000 claims description 9
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 8
- 239000003945 anionic surfactant Substances 0.000 claims description 8
- 150000002170 ethers Chemical class 0.000 claims description 7
- 239000002736 nonionic surfactant Substances 0.000 claims description 6
- 239000004721 Polyphenylene oxide Substances 0.000 claims description 5
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical group CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 claims description 5
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfate Natural products OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims description 5
- 150000007942 carboxylates Chemical class 0.000 claims description 5
- 125000006353 oxyethylene group Chemical group 0.000 claims description 5
- 150000003014 phosphoric acid esters Chemical class 0.000 claims description 5
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 4
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 claims description 4
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 claims description 3
- 125000005702 oxyalkylene group Chemical group 0.000 claims description 2
- 239000000306 component Substances 0.000 claims 18
- 125000000217 alkyl group Chemical group 0.000 claims 7
- 150000004945 aromatic hydrocarbons Chemical class 0.000 claims 3
- 229920001451 polypropylene glycol Polymers 0.000 claims 3
- 229910052799 carbon Inorganic materials 0.000 claims 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical group C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims 1
- 239000005977 Ethylene Substances 0.000 claims 1
- 239000003921 oil Substances 0.000 description 50
- 239000012141 concentrate Substances 0.000 description 46
- 235000008504 concentrate Nutrition 0.000 description 46
- 241000196324 Embryophyta Species 0.000 description 21
- 235000019441 ethanol Nutrition 0.000 description 14
- CSPPKDPQLUUTND-NBVRZTHBSA-N Sethoxydim Chemical compound CCO\N=C(/CCC)C1=C(O)CC(CC(C)SCC)CC1=O CSPPKDPQLUUTND-NBVRZTHBSA-N 0.000 description 9
- 244000025254 Cannabis sativa Species 0.000 description 8
- 125000003118 aryl group Chemical group 0.000 description 7
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 6
- DNIAPMSPPWPWGF-GSVOUGTGSA-N (R)-(-)-Propylene glycol Polymers C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-N 0.000 description 5
- 229910019142 PO4 Inorganic materials 0.000 description 5
- 240000004713 Pisum sativum Species 0.000 description 5
- 235000010582 Pisum sativum Nutrition 0.000 description 5
- 150000001298 alcohols Chemical class 0.000 description 5
- 239000010452 phosphate Substances 0.000 description 5
- 239000005501 Cycloxydim Substances 0.000 description 4
- FLIACVVOZYBSBS-UHFFFAOYSA-N Methyl palmitate Chemical compound CCCCCCCCCCCCCCCC(=O)OC FLIACVVOZYBSBS-UHFFFAOYSA-N 0.000 description 4
- 240000008042 Zea mays Species 0.000 description 4
- 239000002253 acid Substances 0.000 description 4
- GGWHBJGBERXSLL-NBVRZTHBSA-N chembl113137 Chemical compound C1C(=O)C(C(=N/OCC)/CCC)=C(O)CC1C1CSCCC1 GGWHBJGBERXSLL-NBVRZTHBSA-N 0.000 description 4
- USIUVYZYUHIAEV-UHFFFAOYSA-N diphenyl ether Chemical compound C=1C=CC=CC=1OC1=CC=CC=C1 USIUVYZYUHIAEV-UHFFFAOYSA-N 0.000 description 4
- 238000009472 formulation Methods 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- 238000002360 preparation method Methods 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- 244000075850 Avena orientalis Species 0.000 description 3
- 240000005979 Hordeum vulgare Species 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 240000007594 Oryza sativa Species 0.000 description 3
- 235000007164 Oryza sativa Nutrition 0.000 description 3
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 3
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 3
- 125000001931 aliphatic group Chemical group 0.000 description 3
- BFNBIHQBYMNNAN-UHFFFAOYSA-N ammonium sulfate Chemical compound N.N.OS(O)(=O)=O BFNBIHQBYMNNAN-UHFFFAOYSA-N 0.000 description 3
- 229910052921 ammonium sulfate Inorganic materials 0.000 description 3
- 235000011130 ammonium sulphate Nutrition 0.000 description 3
- 239000003849 aromatic solvent Substances 0.000 description 3
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 235000005822 corn Nutrition 0.000 description 3
- 230000035613 defoliation Effects 0.000 description 3
- 239000004615 ingredient Substances 0.000 description 3
- 239000003999 initiator Substances 0.000 description 3
- 229910052500 inorganic mineral Inorganic materials 0.000 description 3
- 239000011707 mineral Substances 0.000 description 3
- 235000009566 rice Nutrition 0.000 description 3
- HIXDQWDOVZUNNA-UHFFFAOYSA-N 2-(3,4-dimethoxyphenyl)-5-hydroxy-7-methoxychromen-4-one Chemical compound C=1C(OC)=CC(O)=C(C(C=2)=O)C=1OC=2C1=CC=C(OC)C(OC)=C1 HIXDQWDOVZUNNA-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 235000007320 Avena fatua Nutrition 0.000 description 2
- 229920000742 Cotton Polymers 0.000 description 2
- 244000052363 Cynodon dactylon Species 0.000 description 2
- 244000058871 Echinochloa crus-galli Species 0.000 description 2
- 244000068988 Glycine max Species 0.000 description 2
- 235000010469 Glycine max Nutrition 0.000 description 2
- 235000007340 Hordeum vulgare Nutrition 0.000 description 2
- 241000207783 Ipomoea Species 0.000 description 2
- 235000021506 Ipomoea Nutrition 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- 235000021314 Palmitic acid Nutrition 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- 229920002257 Plurafac® Polymers 0.000 description 2
- 241000209504 Poaceae Species 0.000 description 2
- 240000002439 Sorghum halepense Species 0.000 description 2
- 241000219793 Trifolium Species 0.000 description 2
- 241000209140 Triticum Species 0.000 description 2
- 235000021307 Triticum Nutrition 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 239000004480 active ingredient Substances 0.000 description 2
- ZOMSMJKLGFBRBS-UHFFFAOYSA-N bentazone Chemical compound C1=CC=C2NS(=O)(=O)N(C(C)C)C(=O)C2=C1 ZOMSMJKLGFBRBS-UHFFFAOYSA-N 0.000 description 2
- FOCAUTSVDIKZOP-UHFFFAOYSA-N chloroacetic acid Chemical compound OC(=O)CCl FOCAUTSVDIKZOP-UHFFFAOYSA-N 0.000 description 2
- 229940106681 chloroacetic acid Drugs 0.000 description 2
- FWFSEYBSWVRWGL-UHFFFAOYSA-N cyclohex-2-enone Chemical compound O=C1CCCC=C1 FWFSEYBSWVRWGL-UHFFFAOYSA-N 0.000 description 2
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
- LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 150000002191 fatty alcohols Chemical class 0.000 description 2
- 239000006260 foam Substances 0.000 description 2
- ZSIAUFGUXNUGDI-UHFFFAOYSA-N hexan-1-ol Chemical compound CCCCCCO ZSIAUFGUXNUGDI-UHFFFAOYSA-N 0.000 description 2
- 150000004702 methyl esters Chemical class 0.000 description 2
- 235000021313 oleic acid Nutrition 0.000 description 2
- 150000002889 oleic acids Chemical class 0.000 description 2
- 150000002943 palmitic acids Chemical class 0.000 description 2
- 239000003208 petroleum Substances 0.000 description 2
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 2
- 241000894007 species Species 0.000 description 2
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 2
- 235000013311 vegetables Nutrition 0.000 description 2
- 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
- YXBDMGSFNUJTBR-NFSGWXFISA-N 2-[(E)-N-[(E)-3-chloroprop-2-enoxy]-C-propylcarbonimidoyl]-5-(2-ethylsulfanylpropyl)-3-hydroxycyclohex-2-en-1-one Chemical compound Cl/C=C/CO\N=C(/CCC)C1=C(O)CC(CC(C)SCC)CC1=O YXBDMGSFNUJTBR-NFSGWXFISA-N 0.000 description 1
- BWDBEAQIHAEVLV-UHFFFAOYSA-N 6-methylheptan-1-ol Chemical compound CC(C)CCCCCO BWDBEAQIHAEVLV-UHFFFAOYSA-N 0.000 description 1
- 241000219144 Abutilon Species 0.000 description 1
- 240000000321 Abutilon grandifolium Species 0.000 description 1
- 239000004254 Ammonium phosphate Substances 0.000 description 1
- 241000209764 Avena fatua Species 0.000 description 1
- 235000007319 Avena orientalis Nutrition 0.000 description 1
- 241000209202 Bromus secalinus Species 0.000 description 1
- 241001148727 Bromus tectorum Species 0.000 description 1
- 240000006122 Chenopodium album Species 0.000 description 1
- 244000298479 Cichorium intybus Species 0.000 description 1
- 235000007542 Cichorium intybus Nutrition 0.000 description 1
- 239000005497 Clethodim Substances 0.000 description 1
- 240000008853 Datura stramonium Species 0.000 description 1
- 244000152970 Digitaria sanguinalis Species 0.000 description 1
- 235000010823 Digitaria sanguinalis Nutrition 0.000 description 1
- 239000005630 Diquat Substances 0.000 description 1
- 241000192043 Echinochloa Species 0.000 description 1
- 241000234643 Festuca arundinacea Species 0.000 description 1
- 241001640034 Heteropterys Species 0.000 description 1
- 101000847066 Homo sapiens Translin-associated protein X Proteins 0.000 description 1
- 240000001549 Ipomoea eriocarpa Species 0.000 description 1
- 241000032989 Ipomoea lacunosa Species 0.000 description 1
- 241000320639 Leptochloa Species 0.000 description 1
- 244000143149 Leptochloa chinensis Species 0.000 description 1
- 235000003403 Limnocharis flava Nutrition 0.000 description 1
- 244000100545 Lolium multiflorum Species 0.000 description 1
- 241001508687 Mustela erminea Species 0.000 description 1
- 235000021360 Myristic acid Nutrition 0.000 description 1
- IGFHQQFPSIBGKE-UHFFFAOYSA-N Nonylphenol Natural products CCCCCCCCCC1=CC=C(O)C=C1 IGFHQQFPSIBGKE-UHFFFAOYSA-N 0.000 description 1
- 239000004435 Oxo alcohol Substances 0.000 description 1
- 241000209048 Poa Species 0.000 description 1
- 244000292693 Poa annua Species 0.000 description 1
- 241000209049 Poa pratensis Species 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
- 241000270295 Serpentes Species 0.000 description 1
- 241001212228 Sesbania drummondii Species 0.000 description 1
- 241001355178 Setaria faberi Species 0.000 description 1
- 244000010062 Setaria pumila Species 0.000 description 1
- 240000003461 Setaria viridis Species 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- HFCYZXMHUIHAQI-UHFFFAOYSA-N Thidiazuron Chemical compound C=1C=CC=CC=1NC(=O)NC1=CN=NS1 HFCYZXMHUIHAQI-UHFFFAOYSA-N 0.000 description 1
- 102100032834 Translin-associated protein X Human genes 0.000 description 1
- 239000007983 Tris buffer Substances 0.000 description 1
- 244000098338 Triticum aestivum Species 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
- 241001141210 Urochloa platyphylla Species 0.000 description 1
- 241001584884 Urochloa texana Species 0.000 description 1
- 235000005373 Uvularia sessilifolia Nutrition 0.000 description 1
- 241001506766 Xanthium Species 0.000 description 1
- 244000067505 Xanthium strumarium Species 0.000 description 1
- 241000209149 Zea Species 0.000 description 1
- 241001148683 Zostera marina Species 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-N acetic acid Substances CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 1
- 230000002152 alkylating effect Effects 0.000 description 1
- 235000020661 alpha-linolenic acid Nutrition 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 229910000148 ammonium phosphate Inorganic materials 0.000 description 1
- 235000019289 ammonium phosphates Nutrition 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 150000001555 benzenes Chemical class 0.000 description 1
- 230000004071 biological effect Effects 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 230000021523 carboxylation Effects 0.000 description 1
- 238000006473 carboxylation reaction Methods 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- SILSDTWXNBZOGF-JWGBMQLESA-N clethodim Chemical compound CCSC(C)CC1CC(O)=C(C(CC)=NOC\C=C\Cl)C(=O)C1 SILSDTWXNBZOGF-JWGBMQLESA-N 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- MNNHAPBLZZVQHP-UHFFFAOYSA-N diammonium hydrogen phosphate Chemical compound [NH4+].[NH4+].OP([O-])([O-])=O MNNHAPBLZZVQHP-UHFFFAOYSA-N 0.000 description 1
- 150000005690 diesters Chemical class 0.000 description 1
- SYJFEGQWDCRVNX-UHFFFAOYSA-N diquat Chemical compound C1=CC=[N+]2CC[N+]3=CC=CC=C3C2=C1 SYJFEGQWDCRVNX-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
- 230000032050 esterification Effects 0.000 description 1
- 238000005886 esterification reaction Methods 0.000 description 1
- 125000004494 ethyl ester group Chemical group 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 239000000417 fungicide Substances 0.000 description 1
- 125000000623 heterocyclic group Chemical group 0.000 description 1
- 239000002917 insecticide Substances 0.000 description 1
- 239000002563 ionic surfactant Substances 0.000 description 1
- 235000020778 linoleic acid Nutrition 0.000 description 1
- OYHQOLUKZRVURQ-HZJYTTRNSA-N linoleic acid group Chemical group C(CCCCCCC\C=C/C\C=C/CCCCC)(=O)O OYHQOLUKZRVURQ-HZJYTTRNSA-N 0.000 description 1
- 125000005481 linolenic acid group Chemical group 0.000 description 1
- 150000004668 long chain fatty acids Chemical class 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 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
- 150000007522 mineralic acids Chemical class 0.000 description 1
- LNOPIUAQISRISI-UHFFFAOYSA-N n'-hydroxy-2-propan-2-ylsulfonylethanimidamide Chemical compound CC(C)S(=O)(=O)CC(N)=NO LNOPIUAQISRISI-UHFFFAOYSA-N 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical compound CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 1
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- FIKAKWIAUPDISJ-UHFFFAOYSA-L paraquat dichloride Chemical compound [Cl-].[Cl-].C1=C[N+](C)=CC=C1C1=CC=[N+](C)C=C1 FIKAKWIAUPDISJ-UHFFFAOYSA-L 0.000 description 1
- 239000000575 pesticide Substances 0.000 description 1
- XHXFXVLFKHQFAL-UHFFFAOYSA-N phosphoryl trichloride Chemical compound ClP(Cl)(Cl)=O XHXFXVLFKHQFAL-UHFFFAOYSA-N 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000005648 plant growth regulator Substances 0.000 description 1
- 229920000137 polyphosphoric acid Polymers 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- DLYUQMMRRRQYAE-UHFFFAOYSA-N tetraphosphorus decaoxide Chemical compound O1P(O2)(=O)OP3(=O)OP1(=O)OP2(=O)O3 DLYUQMMRRRQYAE-UHFFFAOYSA-N 0.000 description 1
- ZFXYFBGIUFBOJW-UHFFFAOYSA-N theophylline Chemical compound O=C1N(C)C(=O)N(C)C2=C1NC=N2 ZFXYFBGIUFBOJW-UHFFFAOYSA-N 0.000 description 1
- 229960000278 theophylline Drugs 0.000 description 1
- JSPLKZUTYZBBKA-UHFFFAOYSA-N trioxidane Chemical compound OOO JSPLKZUTYZBBKA-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
- A01N25/30—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
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S516/00—Colloid systems and wetting agents; subcombinations thereof; processes of
- Y10S516/01—Wetting, emulsifying, dispersing, or stabilizing agents
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S516/00—Colloid systems and wetting agents; subcombinations thereof; processes of
- Y10S516/01—Wetting, emulsifying, dispersing, or stabilizing agents
- Y10S516/03—Organic sulfoxy compound containing
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S516/00—Colloid systems and wetting agents; subcombinations thereof; processes of
- Y10S516/01—Wetting, emulsifying, dispersing, or stabilizing agents
- Y10S516/06—Protein or carboxylic compound containing
Landscapes
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Health & Medical Sciences (AREA)
- Toxicology (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Agronomy & Crop Science (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US07/237,609 US4966728A (en) | 1988-08-26 | 1988-08-26 | Adjuvants for use with postemergent herbicides |
Publications (1)
Publication Number | Publication Date |
---|---|
PH26428A true PH26428A (en) | 1992-07-15 |
Family
ID=22894439
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PH39121A PH26428A (en) | 1988-08-26 | 1989-08-21 | Adjuvants for use with postemergent herbicides |
Country Status (12)
Country | Link |
---|---|
US (1) | US4966728A (ja) |
EP (1) | EP0356812B1 (ja) |
JP (1) | JP2894733B2 (ja) |
KR (1) | KR0144579B1 (ja) |
AU (1) | AU625194B2 (ja) |
BR (1) | BR8904263A (ja) |
DE (1) | DE68908044T2 (ja) |
DK (1) | DK420189A (ja) |
ES (1) | ES2058422T3 (ja) |
IE (1) | IE63658B1 (ja) |
PH (1) | PH26428A (ja) |
ZA (1) | ZA896487B (ja) |
Families Citing this family (30)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5084087A (en) * | 1989-04-26 | 1992-01-28 | Basf Corporation | Ready to dilute adjuvant-containing postemergent herbicide formulations |
US5078781A (en) * | 1989-06-30 | 1992-01-07 | Imperial Chemical Industries Plc | Bipyridilium herbicidal compositions |
USRE37313E1 (en) * | 1990-07-19 | 2001-08-07 | Helena Chemical Company | Homogeneous, essentially nonaqueous adjuvant compositions with buffering capability |
US5580567A (en) * | 1990-07-19 | 1996-12-03 | Helena Chemical Company | Homogeneous, essentially nonaqueous adjuvant compositions with buffering capability |
US5178795A (en) * | 1990-07-19 | 1993-01-12 | Helena Chemical Company | Homogeneous, essentially nonaqueous adjuvant compositions with buffering capability |
US5741502A (en) * | 1990-07-19 | 1998-04-21 | Helena Chemical Co. | Homogeneous, essentially nonaqueous adjuvant compositions with buffering capability |
US5393791A (en) * | 1990-07-19 | 1995-02-28 | Helena Chemical Company | Homogeneous, essentially nonaqueous adjuvant compositions with buffering capability |
DE4029304A1 (de) * | 1990-09-15 | 1992-03-19 | Hoechst Ag | Synergistische herbizide mittel |
EP0553074B1 (en) * | 1990-10-17 | 1996-06-05 | Tomen Corporation | Method and composition for enhancing uptake and transport of bioactive agents in plants |
WO1992011764A1 (en) | 1991-01-08 | 1992-07-23 | Monsanto Company | Improved herbicidal formulation |
NZ241579A (en) * | 1991-03-25 | 1994-04-27 | Becton Dickinson Co | Antimicrobial formulations for treating the skin |
CA2109541A1 (en) * | 1992-12-04 | 1994-06-05 | Thomas J. Ford | Aromatic oil and process for manufacture |
AU751940B2 (en) * | 1993-05-05 | 2002-09-05 | Innovative Chemical Services Pty Ltd | Herbicide, crop desiccant and defoliant adjuvants |
CN1066012C (zh) * | 1993-05-05 | 2001-05-23 | 维多利亚国际化学有限公司 | 除草剂、作物脱水剂及脱叶剂的辅剂 |
AU686552B3 (en) * | 1993-05-05 | 1998-02-05 | Victorian Chemicals International Pty Ltd | Herbicide, crop desiccant and defoliant adjuvant |
AU1713495A (en) * | 1994-02-24 | 1995-09-11 | Imperial Chemical Industries Plc | Adjuvant compositions |
US5612305A (en) * | 1995-01-12 | 1997-03-18 | Huntsman Petrochemical Corporation | Mixed surfactant systems for low foam applications |
US5686384A (en) * | 1995-03-14 | 1997-11-11 | Zeneca Limited | Compatibility agent and method |
US6235300B1 (en) | 1999-01-19 | 2001-05-22 | Amway Corporation | Plant protecting adjuvant containing topped or peaked alcohol alkoxylates and conventional alcohol alkoxylates |
US6514910B1 (en) * | 1999-03-05 | 2003-02-04 | Basf Aktiengesellschaft | Herbicidal mixture containing a 3-heterocyclyl-substituted benzoyl derivative and an adjuvant |
US6566349B1 (en) | 2000-08-28 | 2003-05-20 | Basf Corporation | Safer organophosphorous compositions |
US6890889B1 (en) * | 2000-09-08 | 2005-05-10 | Syngenta Crop Protection, Inc. | Mesotrione formulations |
US6423667B1 (en) | 2001-05-15 | 2002-07-23 | Honeywell International Inc. | Ammonium sulfate suspensions in oils |
DE10156997A1 (de) * | 2001-11-21 | 2003-08-14 | Basf Ag | Verwendung bestimmter Copolymere als Adjuvans und Mittel für den agrotechnischen Bereich |
DE50312724D1 (de) | 2002-04-24 | 2010-07-01 | Basf Se | Verwendung bestimmter alkoholalkoxylate als adjuvans für den agrotechnischen bereich |
US9072294B2 (en) | 2006-02-15 | 2015-07-07 | Cognis Ip Management Gmbh | Emulsifier system and pesticidal formulations containing the emulsifier system |
CA2647798C (en) | 2006-04-07 | 2015-01-27 | Basf Se | Herbicidal mixture, comprising an imidazolinone herbicide and an adjuvant |
GB0907003D0 (en) * | 2009-04-23 | 2009-06-03 | Syngenta Ltd | Formulation |
EP2305030A1 (de) | 2009-09-14 | 2011-04-06 | Bayer CropScience AG | Alkylpolypropylenglycolpolyethylenglycol enthaltende agrochemische Zusammensetzungen |
KR101898920B1 (ko) * | 2010-09-14 | 2018-09-14 | 바스프 에스이 | 피리피로펜 살곤충제 및 애주번트를 함유하는 조성물 |
Family Cites Families (18)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3990884A (en) * | 1969-10-23 | 1976-11-09 | Fisons Limited | Herbicidal Composition Comprising 4-chloro-2-butynyl m-chlorocarbanilate |
US3997322A (en) * | 1970-09-09 | 1976-12-14 | Sun Oil Company Of Pennsylvania | Herbicide carrier oil composition |
US4174960A (en) * | 1977-02-09 | 1979-11-20 | Lilly Industries Limited | Pesticidal formulation |
US4182621A (en) * | 1978-02-01 | 1980-01-08 | Otsuka Kagaku Yakuhin Kabushiki Kaisha | Composition for inhibiting the growth of plants |
CA1120745A (en) * | 1980-03-17 | 1982-03-30 | F. Nelson Keeney | Flowable 2-chloro-n-isopropylacetanilide |
DE3033335A1 (de) * | 1980-09-04 | 1982-04-22 | Lentia GmbH Chem. u. pharm. Erzeugnisse - Industriebedarf, 8000 München | Verfahren zur herstellung einer lagerstabilen, konzentrierten emulsion von herbizid wirkenden phenoxyalkancarbonsaeureestern |
US4557751A (en) * | 1981-03-10 | 1985-12-10 | Minnesota Mining And Manufacturing Company | Compositions containing surfactant and broadleaf foliar herbicide |
PH20618A (en) * | 1982-01-29 | 1987-03-06 | Ici Australia Ltd | Herbicidal 5-(substituted phenyl)-cyclohexan-1,3-dione derivatives |
US4642338A (en) * | 1983-09-01 | 1987-02-10 | The Dow Chemical Company | Fluorophenoxyphenoxypropionates and derivatives thereof |
DE3429437A1 (de) * | 1983-12-08 | 1985-06-20 | Basf Ag, 6700 Ludwigshafen | Cyclohexenonderivate, verfahren zu ihrer herstellung und ihre verwendung zur bekaempfung unerwuenschten pflanzenwuchses |
EP0163598B1 (de) * | 1984-04-27 | 1989-10-04 | Ciba-Geigy Ag | Herbizide Zusammensetzungen |
DE3437238A1 (de) * | 1984-10-11 | 1986-04-17 | Basf Ag, 6700 Ludwigshafen | Neue verbindungen, verfahren zu ihrer herstellung und ihre verwendung zur bekaempfung unerwuenschten pflanzenwuchses |
US4840660A (en) * | 1985-12-30 | 1989-06-20 | Rhone Poulenc Nederlands B.V. | Plant growth regulator dispersions |
DE3614788A1 (de) * | 1986-05-02 | 1987-11-05 | Hoechst Ag | Herbizide emulsionen |
FR2601259B1 (fr) * | 1986-07-11 | 1990-06-22 | Rhone Poulenc Chimie | Nouvelles compositions tensio-actives a base d'esters phosphoriques leur procede de preparation et leur application a la formulation de matieres actives. |
GB8624644D0 (en) * | 1986-10-14 | 1986-11-19 | Ici Plc | Herbicidal compositions |
GB8626246D0 (en) * | 1986-11-03 | 1986-12-03 | Monsanto Europe Sa | Compositions containing glyphosate &c |
US4834908A (en) * | 1987-10-05 | 1989-05-30 | Basf Corporation | Antagonism defeating crop oil concentrates |
-
1988
- 1988-08-26 US US07/237,609 patent/US4966728A/en not_active Expired - Lifetime
-
1989
- 1989-08-17 ES ES89115134T patent/ES2058422T3/es not_active Expired - Lifetime
- 1989-08-17 DE DE89115134T patent/DE68908044T2/de not_active Expired - Lifetime
- 1989-08-17 EP EP89115134A patent/EP0356812B1/en not_active Expired - Lifetime
- 1989-08-21 PH PH39121A patent/PH26428A/en unknown
- 1989-08-23 JP JP1215144A patent/JP2894733B2/ja not_active Expired - Lifetime
- 1989-08-24 BR BR898904263A patent/BR8904263A/pt unknown
- 1989-08-25 DK DK420189A patent/DK420189A/da not_active Application Discontinuation
- 1989-08-25 ZA ZA896487A patent/ZA896487B/xx unknown
- 1989-08-25 AU AU40236/89A patent/AU625194B2/en not_active Expired
- 1989-08-25 IE IE275289A patent/IE63658B1/en not_active IP Right Cessation
- 1989-08-26 KR KR1019890012275A patent/KR0144579B1/ko not_active IP Right Cessation
Also Published As
Publication number | Publication date |
---|---|
AU4023689A (en) | 1990-03-01 |
JP2894733B2 (ja) | 1999-05-24 |
DK420189A (da) | 1990-02-27 |
IE892752L (en) | 1990-02-26 |
DE68908044D1 (de) | 1993-09-09 |
AU625194B2 (en) | 1992-07-02 |
BR8904263A (pt) | 1990-04-10 |
ZA896487B (en) | 1991-04-24 |
EP0356812A2 (en) | 1990-03-07 |
DK420189D0 (da) | 1989-08-25 |
EP0356812A3 (en) | 1991-05-15 |
ES2058422T3 (es) | 1994-11-01 |
US4966728A (en) | 1990-10-30 |
KR0144579B1 (ko) | 1998-07-01 |
EP0356812B1 (en) | 1993-08-04 |
IE63658B1 (en) | 1995-05-31 |
DE68908044T2 (de) | 1993-11-18 |
JPH02152901A (ja) | 1990-06-12 |
KR900002697A (ko) | 1990-03-23 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
PH26428A (en) | Adjuvants for use with postemergent herbicides | |
US4834908A (en) | Antagonism defeating crop oil concentrates | |
US5084087A (en) | Ready to dilute adjuvant-containing postemergent herbicide formulations | |
US5703015A (en) | Pesticidal compositions of polyoxyalkylene alkylamine surfactants having reduced eye irritation | |
US5238604A (en) | Crop oil concentrates | |
US5102442A (en) | Antagonism defeating crop oil concentrates | |
RU2332845C2 (ru) | Системы поверхностно-активное вещество/растворитель | |
KR100232246B1 (ko) | 농업용 제제 | |
CA2047968C (en) | New surfactant compositions, method for their preparation, and pesticidal compositions containing same | |
EP1164842A1 (de) | Flüssige zubereitungen und tensid/lösungsmittel-systeme | |
US9596846B2 (en) | Agricultural pesticide compositions | |
DE60016638T2 (de) | Pestizidformulierungen die als oberflächenaktive Verbindungen Phosphatester und alkoxylierte Lignosulfonate enthalten | |
US2696453A (en) | Emulsifiers and toxicants containing the same | |
DE60023765T2 (de) | Entschäumer enthaltendes Pflanzenschutzmittel-Emulsionskonzentrat | |
USRE24184E (en) | Emulsifiers and toxrcants containing | |
JP2729245B2 (ja) | 高濃度除草製剤 | |
TWI394531B (zh) | 除草組成物 | |
CN101657095A (zh) | 水可悬浮的农业化学组合物 | |
US3185562A (en) | Emulsifiable pesticidal composition | |
EP0542919A1 (en) | EXTENSION FORMULATION WITH SUPPORTING PROPERTIES FOR AGRICULTURAL PRODUCTS. | |
EP2381768A2 (de) | Agrochemische zusammensetzungen umfassend verzweigte alkoxyalkanoate | |
JPH02240001A (ja) | 高濃度除草製剤 |