CA1049536A - Composes herbicides - Google Patents
Composes herbicidesInfo
- Publication number
- CA1049536A CA1049536A CA184,017A CA184017A CA1049536A CA 1049536 A CA1049536 A CA 1049536A CA 184017 A CA184017 A CA 184017A CA 1049536 A CA1049536 A CA 1049536A
- Authority
- CA
- Canada
- Prior art keywords
- anion
- methyl
- dimethyl
- acid
- salt
- Prior art date
- Legal status (The legal status 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 status listed.)
- Expired
Links
- 230000002363 herbicidal effect Effects 0.000 title claims abstract description 20
- 239000000203 mixture Substances 0.000 title description 23
- 150000003839 salts Chemical class 0.000 claims abstract description 32
- 150000001875 compounds Chemical class 0.000 claims abstract description 15
- LCPDWSOZIOUXRV-UHFFFAOYSA-N phenoxyacetic acid Chemical class OC(=O)COC1=CC=CC=C1 LCPDWSOZIOUXRV-UHFFFAOYSA-N 0.000 claims abstract description 15
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims abstract description 13
- 244000025254 Cannabis sativa Species 0.000 claims abstract description 12
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 10
- 229910052736 halogen Inorganic materials 0.000 claims abstract description 9
- 150000002367 halogens Chemical class 0.000 claims abstract description 8
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 7
- 239000001257 hydrogen Substances 0.000 claims abstract description 7
- WTKZEGDFNFYCGP-UHFFFAOYSA-N Pyrazole Chemical group C=1C=NNC=1 WTKZEGDFNFYCGP-UHFFFAOYSA-N 0.000 claims abstract description 6
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims abstract description 3
- 241000196324 Embryophyta Species 0.000 claims description 26
- 239000004009 herbicide Substances 0.000 claims description 20
- -1 polyhalocarboxylate Chemical compound 0.000 claims description 18
- 150000001450 anions Chemical class 0.000 claims description 16
- 239000002253 acid Substances 0.000 claims description 11
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims description 6
- 125000001309 chloro group Chemical group Cl* 0.000 claims description 5
- IQUPABOKLQSFBK-UHFFFAOYSA-N 2-nitrophenol Chemical compound OC1=CC=CC=C1[N+]([O-])=O IQUPABOKLQSFBK-UHFFFAOYSA-N 0.000 claims description 4
- 239000000460 chlorine Substances 0.000 claims description 4
- NDUPDOJHUQKPAG-UHFFFAOYSA-N Dalapon Chemical compound CC(Cl)(Cl)C(O)=O NDUPDOJHUQKPAG-UHFFFAOYSA-N 0.000 claims description 3
- LBGPXIPGGRQBJW-UHFFFAOYSA-N Difenzoquat Chemical compound C[N+]=1N(C)C(C=2C=CC=CC=2)=CC=1C1=CC=CC=C1 LBGPXIPGGRQBJW-UHFFFAOYSA-N 0.000 claims description 3
- 150000001768 cations Chemical class 0.000 claims description 3
- 125000006371 dihalo methyl group Chemical group 0.000 claims description 3
- 125000004970 halomethyl group Chemical group 0.000 claims description 3
- JRIDOENDCAHBEL-UHFFFAOYSA-M 2-(4-chloro-2-methylphenoxy)acetate;1,2-dimethyl-3,5-diphenylpyrazol-1-ium Chemical compound CC1=CC(Cl)=CC=C1OCC([O-])=O.C[N+]=1N(C)C(C=2C=CC=CC=2)=CC=1C1=CC=CC=C1 JRIDOENDCAHBEL-UHFFFAOYSA-M 0.000 claims description 2
- OWZPCEFYPSAJFR-UHFFFAOYSA-N 2-(butan-2-yl)-4,6-dinitrophenol Chemical compound CCC(C)C1=CC([N+]([O-])=O)=CC([N+]([O-])=O)=C1O OWZPCEFYPSAJFR-UHFFFAOYSA-N 0.000 claims description 2
- 229910052801 chlorine Inorganic materials 0.000 claims description 2
- JVKIVZVZEUXPTI-UHFFFAOYSA-M 2-(2,4-dichlorophenoxy)acetate;1,2-dimethyl-3,5-diphenylpyrazol-1-ium Chemical compound [O-]C(=O)COC1=CC=C(Cl)C=C1Cl.C[N+]=1N(C)C(C=2C=CC=CC=2)=CC=1C1=CC=CC=C1 JVKIVZVZEUXPTI-UHFFFAOYSA-M 0.000 claims 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims 1
- 125000004218 chloromethyl group Chemical group [H]C([H])(Cl)* 0.000 claims 1
- 125000004772 dichloromethyl group Chemical group [H]C(Cl)(Cl)* 0.000 claims 1
- 229940031826 phenolate Drugs 0.000 abstract description 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract 1
- 229910052799 carbon Inorganic materials 0.000 abstract 1
- 150000002431 hydrogen Chemical class 0.000 abstract 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 1
- 150000004707 phenolate Chemical class 0.000 abstract 1
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 30
- 235000007320 Avena fatua Nutrition 0.000 description 24
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 24
- 244000075850 Avena orientalis Species 0.000 description 17
- 235000005373 Uvularia sessilifolia Nutrition 0.000 description 16
- 229910001868 water Inorganic materials 0.000 description 14
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 12
- 239000000243 solution Substances 0.000 description 12
- 241001647031 Avena sterilis Species 0.000 description 10
- 229940022682 acetone Drugs 0.000 description 10
- 235000004535 Avena sterilis Nutrition 0.000 description 9
- 239000004094 surface-active agent Substances 0.000 description 9
- 239000003921 oil Substances 0.000 description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
- 239000005631 2,4-Dichlorophenoxyacetic acid Substances 0.000 description 7
- 238000002360 preparation method Methods 0.000 description 7
- 239000007787 solid Substances 0.000 description 7
- 241000209504 Poaceae Species 0.000 description 6
- 150000002148 esters Chemical class 0.000 description 6
- 238000009472 formulation Methods 0.000 description 6
- 238000000034 method Methods 0.000 description 5
- 235000001602 Digitaria X umfolozi Nutrition 0.000 description 4
- 235000017898 Digitaria ciliaris Nutrition 0.000 description 4
- 235000005476 Digitaria cruciata Nutrition 0.000 description 4
- 235000006830 Digitaria didactyla Nutrition 0.000 description 4
- 235000005804 Digitaria eriantha ssp. eriantha Nutrition 0.000 description 4
- 235000010823 Digitaria sanguinalis Nutrition 0.000 description 4
- 244000058871 Echinochloa crus-galli Species 0.000 description 4
- 244000025670 Eleusine indica Species 0.000 description 4
- 235000014716 Eleusine indica Nutrition 0.000 description 4
- 238000001704 evaporation Methods 0.000 description 4
- 230000003054 hormonal effect Effects 0.000 description 4
- 229920000056 polyoxyethylene ether Polymers 0.000 description 4
- 239000007921 spray Substances 0.000 description 4
- BGCSXGXXLDPSHB-UHFFFAOYSA-M 1,2-dimethyl-3,5-diphenylpyrazol-1-ium;hydroxide Chemical compound [OH-].C[N+]=1N(C)C(C=2C=CC=CC=2)=CC=1C1=CC=CC=C1 BGCSXGXXLDPSHB-UHFFFAOYSA-M 0.000 description 3
- NDUPDOJHUQKPAG-UHFFFAOYSA-M 2,2-Dichloropropanoate Chemical compound CC(Cl)(Cl)C([O-])=O NDUPDOJHUQKPAG-UHFFFAOYSA-M 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- 240000004713 Pisum sativum Species 0.000 description 3
- 235000010582 Pisum sativum Nutrition 0.000 description 3
- 240000003461 Setaria viridis Species 0.000 description 3
- 235000002248 Setaria viridis Nutrition 0.000 description 3
- 235000010086 Setaria viridis var. viridis Nutrition 0.000 description 3
- WHKUVVPPKQRRBV-UHFFFAOYSA-N Trasan Chemical compound CC1=CC(Cl)=CC=C1OCC(O)=O WHKUVVPPKQRRBV-UHFFFAOYSA-N 0.000 description 3
- 238000004458 analytical method Methods 0.000 description 3
- 125000004432 carbon atom Chemical group C* 0.000 description 3
- IWEDIXLBFLAXBO-UHFFFAOYSA-N dicamba Chemical compound COC1=C(Cl)C=CC(Cl)=C1C(O)=O IWEDIXLBFLAXBO-UHFFFAOYSA-N 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 125000005843 halogen group Chemical group 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 230000008018 melting Effects 0.000 description 3
- 238000002844 melting Methods 0.000 description 3
- 239000004563 wettable powder Substances 0.000 description 3
- UFBJCMHMOXMLKC-UHFFFAOYSA-N 2,4-dinitrophenol Chemical compound OC1=CC=C([N+]([O-])=O)C=C1[N+]([O-])=O UFBJCMHMOXMLKC-UHFFFAOYSA-N 0.000 description 2
- 241000219310 Beta vulgaris subsp. vulgaris Species 0.000 description 2
- 239000005504 Dicamba Substances 0.000 description 2
- 244000020551 Helianthus annuus Species 0.000 description 2
- 235000003222 Helianthus annuus Nutrition 0.000 description 2
- 240000005979 Hordeum vulgare Species 0.000 description 2
- 235000007340 Hordeum vulgare Nutrition 0.000 description 2
- 235000004431 Linum usitatissimum Nutrition 0.000 description 2
- 240000006240 Linum usitatissimum Species 0.000 description 2
- 239000005574 MCPA Substances 0.000 description 2
- 229920001213 Polysorbate 20 Polymers 0.000 description 2
- WTKZEGDFNFYCGP-UHFFFAOYSA-O Pyrazolium Chemical compound C1=CN[NH+]=C1 WTKZEGDFNFYCGP-UHFFFAOYSA-O 0.000 description 2
- 235000007238 Secale cereale Nutrition 0.000 description 2
- 244000082988 Secale cereale Species 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 235000021536 Sugar beet Nutrition 0.000 description 2
- 235000021307 Triticum Nutrition 0.000 description 2
- 244000098338 Triticum aestivum Species 0.000 description 2
- 241001148683 Zostera marina Species 0.000 description 2
- 239000004480 active ingredient Substances 0.000 description 2
- 125000003545 alkoxy group Chemical group 0.000 description 2
- MCOQHIWZJUDQIC-UHFFFAOYSA-N barban Chemical compound ClCC#CCOC(=O)NC1=CC=CC(Cl)=C1 MCOQHIWZJUDQIC-UHFFFAOYSA-N 0.000 description 2
- 125000001246 bromo group Chemical group Br* 0.000 description 2
- 239000004495 emulsifiable concentrate Substances 0.000 description 2
- 150000002170 ethers Chemical class 0.000 description 2
- 125000001153 fluoro group Chemical group F* 0.000 description 2
- 238000003359 percent control normalization Methods 0.000 description 2
- 229940051841 polyoxyethylene ether Drugs 0.000 description 2
- 239000000256 polyoxyethylene sorbitan monolaurate Substances 0.000 description 2
- 235000010486 polyoxyethylene sorbitan monolaurate Nutrition 0.000 description 2
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 2
- 239000012085 test solution Substances 0.000 description 2
- XQEMNBNCQVQXMO-UHFFFAOYSA-M 1,2-dimethyl-3,5-diphenylpyrazol-1-ium;methyl sulfate Chemical compound COS([O-])(=O)=O.C[N+]=1N(C)C(C=2C=CC=CC=2)=CC=1C1=CC=CC=C1 XQEMNBNCQVQXMO-UHFFFAOYSA-M 0.000 description 1
- GBNOSMRRYYJCFQ-UHFFFAOYSA-N 1h-pyrazole;hydrate Chemical compound O.C=1C=NNC=1 GBNOSMRRYYJCFQ-UHFFFAOYSA-N 0.000 description 1
- BMTRHSLGCDHDNQ-UHFFFAOYSA-M 2,2-dichloropropanoate;1,2-dimethyl-3,5-diphenylpyrazol-1-ium Chemical compound CC(Cl)(Cl)C([O-])=O.C[N+]=1N(C)C(C=2C=CC=CC=2)=CC=1C1=CC=CC=C1 BMTRHSLGCDHDNQ-UHFFFAOYSA-M 0.000 description 1
- MHKBMNACOMRIAW-UHFFFAOYSA-N 2,3-dinitrophenol Chemical class OC1=CC=CC([N+]([O-])=O)=C1[N+]([O-])=O MHKBMNACOMRIAW-UHFFFAOYSA-N 0.000 description 1
- OVSKIKFHRZPJSS-UHFFFAOYSA-N 2,4-D Chemical compound OC(=O)COC1=CC=C(Cl)C=C1Cl OVSKIKFHRZPJSS-UHFFFAOYSA-N 0.000 description 1
- HXKWSTRRCHTUEC-UHFFFAOYSA-N 2,4-Dichlorophenoxyaceticacid Chemical compound OC(=O)C(Cl)OC1=CC=C(Cl)C=C1 HXKWSTRRCHTUEC-UHFFFAOYSA-N 0.000 description 1
- YVXAXEOSAXSBQY-UHFFFAOYSA-N 2-chloro-2-(2-methylphenoxy)acetic acid Chemical compound CC1=CC=CC=C1OC(Cl)C(O)=O YVXAXEOSAXSBQY-UHFFFAOYSA-N 0.000 description 1
- DYBIGIADVHIODH-UHFFFAOYSA-N 2-nonylphenol;oxirane Chemical compound C1CO1.CCCCCCCCCC1=CC=CC=C1O DYBIGIADVHIODH-UHFFFAOYSA-N 0.000 description 1
- UPMXNNIRAGDFEH-UHFFFAOYSA-N 3,5-dibromo-4-hydroxybenzonitrile Chemical compound OC1=C(Br)C=C(C#N)C=C1Br UPMXNNIRAGDFEH-UHFFFAOYSA-N 0.000 description 1
- 239000005995 Aluminium silicate Substances 0.000 description 1
- 235000005781 Avena Nutrition 0.000 description 1
- 235000011635 Avena sterilis subsp ludoviciana Nutrition 0.000 description 1
- 239000005489 Bromoxynil Substances 0.000 description 1
- 235000005979 Citrus limon Nutrition 0.000 description 1
- 244000131522 Citrus pyriformis Species 0.000 description 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- QNAYBMKLOCPYGJ-REOHCLBHSA-N L-alanine Chemical compound C[C@H](N)C(O)=O QNAYBMKLOCPYGJ-REOHCLBHSA-N 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- 244000061456 Solanum tuberosum Species 0.000 description 1
- 235000002595 Solanum tuberosum Nutrition 0.000 description 1
- 241000244317 Tillandsia usneoides Species 0.000 description 1
- 238000010669 acid-base reaction Methods 0.000 description 1
- 239000002671 adjuvant Substances 0.000 description 1
- 230000009418 agronomic effect Effects 0.000 description 1
- 235000004279 alanine Nutrition 0.000 description 1
- 125000002877 alkyl aryl group Chemical group 0.000 description 1
- 125000004644 alkyl sulfinyl group Chemical group 0.000 description 1
- 125000004390 alkyl sulfonyl group Chemical group 0.000 description 1
- 125000004414 alkyl thio group Chemical group 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 230000003042 antagnostic effect Effects 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 239000003849 aromatic solvent Substances 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 229960000892 attapulgite Drugs 0.000 description 1
- 235000013877 carbamide Nutrition 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 125000003636 chemical group Chemical group 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 125000000753 cycloalkyl group Chemical group 0.000 description 1
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 1
- SPCNPOWOBZQWJK-UHFFFAOYSA-N dimethoxy-(2-propan-2-ylsulfanylethylsulfanyl)-sulfanylidene-$l^{5}-phosphane Chemical compound COP(=S)(OC)SCCSC(C)C SPCNPOWOBZQWJK-UHFFFAOYSA-N 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 125000004494 ethyl ester group Chemical group 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 230000009969 flowable effect Effects 0.000 description 1
- 238000001640 fractional crystallisation Methods 0.000 description 1
- 125000000623 heterocyclic group Chemical group 0.000 description 1
- 125000002346 iodo group Chemical group I* 0.000 description 1
- 238000005342 ion exchange Methods 0.000 description 1
- 238000004255 ion exchange chromatography Methods 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 238000002955 isolation Methods 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- 239000003350 kerosene Substances 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- ZTMKADLOSYKWCA-UHFFFAOYSA-N lenacil Chemical compound O=C1NC=2CCCC=2C(=O)N1C1CCCCC1 ZTMKADLOSYKWCA-UHFFFAOYSA-N 0.000 description 1
- 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 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- 229910052625 palygorskite Inorganic materials 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-M phenolate Chemical compound [O-]C1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-M 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- PWXJULSLLONQHY-UHFFFAOYSA-N phenylcarbamic acid Chemical class OC(=O)NC1=CC=CC=C1 PWXJULSLLONQHY-UHFFFAOYSA-N 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920000151 polyglycol Polymers 0.000 description 1
- 239000010695 polyglycol Substances 0.000 description 1
- 235000012015 potatoes Nutrition 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 229920005552 sodium lignosulfonate Polymers 0.000 description 1
- PDEFQWNXOUGDJR-UHFFFAOYSA-M sodium;2,2-dichloropropanoate Chemical compound [Na+].CC(Cl)(Cl)C([O-])=O PDEFQWNXOUGDJR-UHFFFAOYSA-M 0.000 description 1
- 150000003918 triazines Chemical class 0.000 description 1
- 150000003672 ureas Chemical class 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/12—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
-
- 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
- A01N39/00—Biocides, pest repellants or attractants, or plant growth regulators containing aryloxy- or arylthio-aliphatic or cycloaliphatic compounds, containing the group or, e.g. phenoxyethylamine, phenylthio-acetonitrile, phenoxyacetone
- A01N39/02—Aryloxy-carboxylic acids; Derivatives thereof
- A01N39/04—Aryloxy-acetic acids; Derivatives thereof
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
- A01N43/56—1,2-Diazoles; Hydrogenated 1,2-diazoles
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Dentistry (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Plant Pathology (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CA314,271A CA1080498A (fr) | 1972-11-17 | 1978-10-25 | Herbicides |
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US30768972A | 1972-11-17 | 1972-11-17 | |
| US00307671A US3857692A (en) | 1972-11-17 | 1972-11-17 | 1,2-dimethyl-3,5-diphenylpyrazolium salts and 3,5-dibromo-4-hydroxybenzonitrile herbicidal compositions |
| US307670A US3867403A (en) | 1972-11-17 | 1972-11-17 | 1,2-dialkyl-3,5-diphenylpyrazolium salts |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA1049536A true CA1049536A (fr) | 1979-02-27 |
Family
ID=27405270
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA184,017A Expired CA1049536A (fr) | 1972-11-17 | 1973-10-23 | Composes herbicides |
Country Status (21)
| Country | Link |
|---|---|
| JP (1) | JPS5747643B2 (fr) |
| AR (1) | AR218206A1 (fr) |
| BR (1) | BR7308966D0 (fr) |
| CA (1) | CA1049536A (fr) |
| CH (1) | CH585002A5 (fr) |
| DD (1) | DD111275A5 (fr) |
| DE (1) | DE2355242C2 (fr) |
| DK (1) | DK137665B (fr) |
| FI (1) | FI55926C (fr) |
| FR (1) | FR2206907B1 (fr) |
| GB (1) | GB1454907A (fr) |
| IE (1) | IE38409B1 (fr) |
| IL (1) | IL43559A (fr) |
| IT (1) | IT1047934B (fr) |
| NL (1) | NL183561C (fr) |
| NO (1) | NO141184C (fr) |
| PL (1) | PL93753B1 (fr) |
| SE (1) | SE421103B (fr) |
| SU (1) | SU589884A3 (fr) |
| TR (1) | TR17383A (fr) |
| YU (1) | YU40095B (fr) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0024188A1 (fr) * | 1979-08-14 | 1981-02-25 | Fbc Limited | Herbicides contenant du difenzoquat |
| JPS6227037Y2 (fr) * | 1980-10-28 | 1987-07-10 | ||
| JPH0516338Y2 (fr) * | 1989-03-28 | 1993-04-28 | ||
| PL382404A1 (pl) * | 2007-05-11 | 2008-11-24 | Zakłady Chemiczne ORGANIKA-SARZYNA Spółka Akcyjna | Nowe pary jonowe zawierające anion (4-chloro-2-metylofenoksy)octanowy i sposób ich wytwarzania |
| PL237908B1 (pl) * | 2018-02-01 | 2021-06-14 | Przed Produkcyjno Consultingowe Adob Spolka Z Ograniczona Odpowiedzialnoscia Spolka Komandytowa | Herbicydowa ciecz jonowa z anionem kwasu 4-chloro-2-metylofenoksyoctowego i zawierająca ją mieszanina eutektyczna |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2260485C2 (de) * | 1971-12-17 | 1983-12-29 | American Cyanamid Co., Wayne, N.J. | 1,2-Dialkyl-3,5-diphenylpyrazoliumsalze und diese enthaltende herbizide Mittel |
| US3922161A (en) * | 1972-11-17 | 1975-11-25 | American Cyanamid Co | Novel herbicidal compositions |
-
1973
- 1973-10-23 CA CA184,017A patent/CA1049536A/fr not_active Expired
- 1973-10-23 IE IE1903/73A patent/IE38409B1/xx unknown
- 1973-11-05 DE DE2355242A patent/DE2355242C2/de not_active Expired
- 1973-11-05 IL IL43559A patent/IL43559A/xx unknown
- 1973-11-05 AR AR250836A patent/AR218206A1/es active
- 1973-11-06 TR TR17383A patent/TR17383A/xx unknown
- 1973-11-08 GB GB5196673A patent/GB1454907A/en not_active Expired
- 1973-11-13 YU YU2922/73A patent/YU40095B/xx unknown
- 1973-11-14 BR BR8966/73A patent/BR7308966D0/pt unknown
- 1973-11-14 NL NLAANVRAGE7315588,A patent/NL183561C/xx not_active IP Right Cessation
- 1973-11-15 CH CH1608673A patent/CH585002A5/xx not_active IP Right Cessation
- 1973-11-15 DK DK618173AA patent/DK137665B/da not_active IP Right Cessation
- 1973-11-16 DD DD174700A patent/DD111275A5/xx unknown
- 1973-11-16 FR FR7340995A patent/FR2206907B1/fr not_active Expired
- 1973-11-16 SU SU731972713A patent/SU589884A3/ru active
- 1973-11-16 PL PL1973166588A patent/PL93753B1/pl unknown
- 1973-11-16 NO NO4407/73A patent/NO141184C/no unknown
- 1973-11-16 FI FI3551/73A patent/FI55926C/fi active
- 1973-11-16 IT IT53751/73A patent/IT1047934B/it active
- 1973-11-16 SE SE7315581A patent/SE421103B/sv unknown
- 1973-11-17 JP JP48128815A patent/JPS5747643B2/ja not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| DE2355242A1 (de) | 1974-05-22 |
| IE38409B1 (en) | 1978-03-01 |
| IL43559A (en) | 1978-09-29 |
| NL7315588A (fr) | 1974-05-21 |
| AU6190873A (en) | 1975-05-01 |
| JPS5747643B2 (fr) | 1982-10-12 |
| YU40095B (en) | 1985-08-31 |
| IE38409L (en) | 1974-05-17 |
| NO141184C (no) | 1980-01-30 |
| FI55926B (fi) | 1979-07-31 |
| DE2355242C2 (de) | 1985-08-08 |
| TR17383A (tr) | 1975-03-24 |
| NL183561B (nl) | 1988-07-01 |
| DD111275A5 (fr) | 1975-02-12 |
| CH585002A5 (fr) | 1977-02-28 |
| DK137665C (fr) | 1978-11-20 |
| SU589884A3 (ru) | 1978-01-25 |
| FR2206907A1 (fr) | 1974-06-14 |
| BR7308966D0 (pt) | 1974-08-22 |
| NL183561C (nl) | 1988-12-01 |
| SE421103B (sv) | 1981-11-30 |
| FI55926C (fi) | 1979-11-12 |
| DK137665B (da) | 1978-04-17 |
| FR2206907B1 (fr) | 1977-06-10 |
| PL93753B1 (en) | 1977-06-30 |
| IT1047934B (it) | 1980-10-20 |
| AR218206A1 (es) | 1980-05-30 |
| GB1454907A (en) | 1976-11-10 |
| NO141184B (no) | 1979-10-22 |
| YU292273A (en) | 1982-06-30 |
| JPS504242A (fr) | 1975-01-17 |
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