PH26428A - Adjuvants for use with postemergent herbicides - Google Patents

Adjuvants for use with postemergent herbicides Download PDF

Info

Publication number: PH26428A
Authority: PH; Philippines
Prior art keywords: percent; component; adjuvant; group; weight
Prior art date: 1988-08-26

Application number

PH39121A

Other languages

English (en)

Inventor

James Lyle Hazen

Original Assignee

Basf Corp

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1988-08-26

Filing date

1989-08-21

Publication date

1992-07-15

1989-08-21 Application filed by Basf Corp filed Critical Basf Corp

1992-07-15 Publication of PH26428A publication Critical patent/PH26428A/en

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)

PH39121A 1988-08-26 1989-08-21 Adjuvants for use with postemergent herbicides PH26428A (en)

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 (de)
EP (1)	EP0356812B1 (de)
JP (1)	JP2894733B2 (de)
KR (1)	KR0144579B1 (de)
AU (1)	AU625194B2 (de)
BR (1)	BR8904263A (de)
DE (1)	DE68908044T2 (de)
DK (1)	DK420189A (de)
ES (1)	ES2058422T3 (de)
IE (1)	IE63658B1 (de)
PH (1)	PH26428A (de)
ZA (1)	ZA896487B (de)

Families Citing this family (31)

* Cited by examiner, † Cited by third party
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
US5580567A (en) *	1990-07-19	1996-12-03	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
USRE37313E1 (en) *	1990-07-19	2001-08-07	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
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 (de) *	1990-10-17	1996-06-05	Tomen Corporation	Verfahren und zusammensetzung zur erhöhung der aufnahme und des transportes bioaktiver wirkstoffe in pflanzen
DE69110907T3 (de)	1991-01-08	2002-03-28	Monsanto Co. (N.D.Ges.D.Staates Delaware), St. Louis	Herbizide formulierung.
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
AU686552B3 (en) *	1993-05-05	1998-02-05	Victorian Chemicals International Pty Ltd	Herbicide, crop desiccant and defoliant adjuvant
CA2160896C (en) *	1993-05-05	2000-07-11	Victorian Chemical International Pty. Ltd.	Herbicide, crop desiccant and defoliant adjuvants
CZ248496A3 (en) *	1994-02-24	1996-12-11	Ici Plc	Auxiliary compositions, concentrate in which the auxiliary composition is comprised, diluted formulation containing such concentrate and method of treating plants and metals therewith
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
UA72505C2 (uk) *	1999-03-05	2005-03-15	Басф Акцієнгезелльшафт	Гербіцидна суміш, що містить заміщену 3-гетероциклілом похідну бензоїлу і допоміжний агент, спосіб її одержання та спосіб боротьби з небажаною рослинністю
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
CA2482758C (en)	2002-04-24	2011-06-14	Basf Aktiengesellschaft	Use of defined alcohol alkoxylates as adjuvants in the agrotechnical field
US9072294B2 (en)	2006-02-15	2015-07-07	Cognis Ip Management Gmbh	Emulsifier system and pesticidal formulations containing the emulsifier system
US20090176648A1 (en) *	2006-04-07	2009-07-09	Thomas Byrne	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
TWI826442B (zh) *	2018-04-30	2023-12-21	美商世多樂集團公司	含有至少一吉貝素化合物與水楊酸之協同性調配物

Family Cites Families (18)

* Cited by examiner, † Cited by third party
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
DE3573368D1 (en) *	1984-04-27	1989-11-09	Ciba Geigy Ag	Herbicidal compositions
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 EP EP89115134A patent/EP0356812B1/de not_active Expired - Lifetime
- 1989-08-17 DE DE89115134T patent/DE68908044T2/de 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 ZA ZA896487A patent/ZA896487B/xx unknown
- 1989-08-25 DK DK420189A patent/DK420189A/da not_active Application Discontinuation
- 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 Expired - Lifetime

Also Published As

Publication number	Publication date
AU625194B2 (en)	1992-07-02
AU4023689A (en)	1990-03-01
KR900002697A (ko)	1990-03-23
BR8904263A (pt)	1990-04-10
EP0356812A2 (de)	1990-03-07
ES2058422T3 (es)	1994-11-01
IE63658B1 (en)	1995-05-31
US4966728A (en)	1990-10-30
DE68908044T2 (de)	1993-11-18
EP0356812B1 (de)	1993-08-04
ZA896487B (en)	1991-04-24
KR0144579B1 (ko)	1998-07-01
DK420189D0 (da)	1989-08-25
EP0356812A3 (de)	1991-05-15
JP2894733B2 (ja)	1999-05-24
DE68908044D1 (de)	1993-09-09
IE892752L (en)	1990-02-26
DK420189A (da)	1990-02-27
JPH02152901A (ja)	1990-06-12

Publication	Publication Date	Title
US4966728A (en)	1990-10-30	Adjuvants for use with postemergent herbicides
US4834908A (en)	1989-05-30	Antagonism defeating crop oil concentrates
US5084087A (en)	1992-01-28	Ready to dilute adjuvant-containing postemergent herbicide formulations
US5238604A (en)	1993-08-24	Crop oil concentrates
US5102442A (en)	1992-04-07	Antagonism defeating crop oil concentrates
US5703015A (en)	1997-12-30	Pesticidal compositions of polyoxyalkylene alkylamine surfactants having reduced eye irritation
EP1164842B1 (de)	2004-02-18	Flüssige zubereitungen und tensid/lösungsmittel-systeme
RU2332845C2 (ru)	2008-09-10	Системы поверхностно-активное вещество/растворитель
US9596846B2 (en)	2017-03-21	Agricultural pesticide compositions
EP0672346B1 (de)	2002-11-06	Neue Tensidezusammensetzungen, Verfahren zu ihrer Herstellung und diese enhaltende Pestizidezusammensetzungen
CA2138965A1 (en)	1994-11-10	Agricultural formulations
US2696453A (en)	1954-12-07	Emulsifiers and toxicants containing the same
EP2790502B1 (de)	2017-07-19	Aromatische phosphatester als komponente einer agrochemischen formulierung
JP6405840B2 (ja)	2018-10-17	水性懸濁状除草剤組成物
JP2729245B2 (ja)	1998-03-18	高濃度除草製剤
TWI394531B (zh)	2013-05-01	除草組成物
JP2832534B2 (ja)	1998-12-09	高濃度除草製剤
EP0542919A1 (de)	1993-05-26	Streckungsmittelformulierung mit unterstützenden eigenschaften für landwirtschaftliche produkte.
EP2381768A2 (de)	2011-11-02	Agrochemische zusammensetzungen umfassend verzweigte alkoxyalkanoate