CA1311937C - Herbicidal compositions - Google Patents
Herbicidal compositionsInfo
- Publication number
- CA1311937C CA1311937C CA000560536A CA560536A CA1311937C CA 1311937 C CA1311937 C CA 1311937C CA 000560536 A CA000560536 A CA 000560536A CA 560536 A CA560536 A CA 560536A CA 1311937 C CA1311937 C CA 1311937C
- Authority
- CA
- Canada
- Prior art keywords
- chloroacetyl
- formula
- composition according
- herbicidal composition
- microcapsules
- 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 - Lifetime
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 71
- 230000002363 herbicidal effect Effects 0.000 title claims abstract description 34
- 239000003094 microcapsule Substances 0.000 claims abstract description 71
- YTWKCBYYGUJDQD-UHFFFAOYSA-N 2-chloro-n-(cyclohexen-1-yl)acetamide Chemical compound ClCC(=O)NC1=CCCCC1 YTWKCBYYGUJDQD-UHFFFAOYSA-N 0.000 claims abstract description 38
- 239000002775 capsule Substances 0.000 claims abstract description 30
- VONWPEXRCLHKRJ-UHFFFAOYSA-N 2-chloro-n-phenylacetamide Chemical compound ClCC(=O)NC1=CC=CC=C1 VONWPEXRCLHKRJ-UHFFFAOYSA-N 0.000 claims abstract description 16
- 229920002396 Polyurea Polymers 0.000 claims abstract description 13
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims description 57
- 229920000642 polymer Polymers 0.000 claims description 31
- WVQBLGZPHOPPFO-UHFFFAOYSA-N 2-chloro-N-(2-ethyl-6-methylphenyl)-N-(1-methoxypropan-2-yl)acetamide Chemical compound CCC1=CC=CC(C)=C1N(C(C)COC)C(=O)CCl WVQBLGZPHOPPFO-UHFFFAOYSA-N 0.000 claims description 22
- 239000002904 solvent Substances 0.000 claims description 20
- 229920000768 polyamine Polymers 0.000 claims description 18
- 238000000034 method Methods 0.000 claims description 17
- 239000005056 polyisocyanate Substances 0.000 claims description 14
- 230000008569 process Effects 0.000 claims description 14
- 229920001228 polyisocyanate Polymers 0.000 claims description 13
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims description 10
- 239000008346 aqueous phase Substances 0.000 claims description 10
- 150000001875 compounds Chemical class 0.000 claims description 10
- 238000002360 preparation method Methods 0.000 claims description 10
- XCSGPAVHZFQHGE-UHFFFAOYSA-N alachlor Chemical compound CCC1=CC=CC(CC)=C1N(COC)C(=O)CCl XCSGPAVHZFQHGE-UHFFFAOYSA-N 0.000 claims description 9
- 239000007900 aqueous suspension Substances 0.000 claims description 9
- 239000000463 material Substances 0.000 claims description 9
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 claims description 9
- 229910052739 hydrogen Inorganic materials 0.000 claims description 8
- 239000001257 hydrogen Substances 0.000 claims description 8
- 239000007788 liquid Substances 0.000 claims description 8
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 8
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 claims description 6
- QNVKMXGRFVLMBM-UHFFFAOYSA-N n-chloro-n-phenylacetamide Chemical compound CC(=O)N(Cl)C1=CC=CC=C1 QNVKMXGRFVLMBM-UHFFFAOYSA-N 0.000 claims description 6
- RFFLAFLAYFXFSW-UHFFFAOYSA-N 1,2-dichlorobenzene Chemical compound ClC1=CC=CC=C1Cl RFFLAFLAYFXFSW-UHFFFAOYSA-N 0.000 claims description 5
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 5
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 claims description 4
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 claims description 4
- SCCDDNKJYDZXMM-UHFFFAOYSA-N dimethachlor Chemical compound COCCN(C(=O)CCl)C1=C(C)C=CC=C1C SCCDDNKJYDZXMM-UHFFFAOYSA-N 0.000 claims description 4
- 239000006185 dispersion Substances 0.000 claims description 4
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims description 3
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims description 3
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 claims description 3
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 claims description 3
- 150000002431 hydrogen Chemical class 0.000 claims description 3
- 239000002480 mineral oil Substances 0.000 claims description 3
- 235000010446 mineral oil Nutrition 0.000 claims description 3
- PPQSFEHBFHOQIH-UHFFFAOYSA-N 1-[2-(chloroamino)cyclohexen-1-yl]ethanone Chemical compound ClNC1=C(CCCC1)C(C)=O PPQSFEHBFHOQIH-UHFFFAOYSA-N 0.000 claims description 2
- NGNBDVOYPDDBFK-UHFFFAOYSA-N 2-[2,4-di(pentan-2-yl)phenoxy]acetyl chloride Chemical compound CCCC(C)C1=CC=C(OCC(Cl)=O)C(C(C)CCC)=C1 NGNBDVOYPDDBFK-UHFFFAOYSA-N 0.000 claims description 2
- IWBVPTHEQYNDFB-UHFFFAOYSA-N 2-chloro-n-(1-methoxypropan-2-yl)-n-(2-methylphenyl)acetamide Chemical compound COCC(C)N(C(=O)CCl)C1=CC=CC=C1C IWBVPTHEQYNDFB-UHFFFAOYSA-N 0.000 claims description 2
- NXFSZAARYUBOBT-UHFFFAOYSA-N 2-chloro-n-(2,6-diethylphenyl)-n-(1-methoxypropan-2-yl)acetamide Chemical compound CCC1=CC=CC(CC)=C1N(C(C)COC)C(=O)CCl NXFSZAARYUBOBT-UHFFFAOYSA-N 0.000 claims description 2
- STLBIPCVNZLGSV-UHFFFAOYSA-N 2-chloro-n-(2,6-diethylphenyl)-n-(2-methoxyethyl)acetamide Chemical compound CCC1=CC=CC(CC)=C1N(CCOC)C(=O)CCl STLBIPCVNZLGSV-UHFFFAOYSA-N 0.000 claims description 2
- QRMXVCIROCSOPW-UHFFFAOYSA-N 2-chloro-n-(2,6-dimethylphenyl)-n-(1-methoxybutan-2-yl)acetamide Chemical compound COCC(CC)N(C(=O)CCl)C1=C(C)C=CC=C1C QRMXVCIROCSOPW-UHFFFAOYSA-N 0.000 claims description 2
- KJYQOYQOCGXPLR-UHFFFAOYSA-N 2-chloro-n-(2,6-dimethylphenyl)-n-(1-methoxypropan-2-yl)acetamide Chemical compound COCC(C)N(C(=O)CCl)C1=C(C)C=CC=C1C KJYQOYQOCGXPLR-UHFFFAOYSA-N 0.000 claims description 2
- DWPUVHBGUBPRQS-UHFFFAOYSA-N 2-chloro-n-(2,6-dimethylphenyl)-n-(2-methoxypropyl)acetamide Chemical compound COC(C)CN(C(=O)CCl)C1=C(C)C=CC=C1C DWPUVHBGUBPRQS-UHFFFAOYSA-N 0.000 claims description 2
- ODHYTKMLSKYOOS-UHFFFAOYSA-N 2-chloro-n-(2,6-dimethylphenyl)-n-(2-propan-2-yloxyethyl)acetamide Chemical compound CC(C)OCCN(C(=O)CCl)C1=C(C)C=CC=C1C ODHYTKMLSKYOOS-UHFFFAOYSA-N 0.000 claims description 2
- NIZACMDZBQKMTD-UHFFFAOYSA-N 2-chloro-n-(2,6-dimethylphenyl)-n-(2-propoxyethyl)acetamide Chemical compound CCCOCCN(C(=O)CCl)C1=C(C)C=CC=C1C NIZACMDZBQKMTD-UHFFFAOYSA-N 0.000 claims description 2
- NZKNDSNFQUHUDF-UHFFFAOYSA-N 2-chloro-n-(2,6-dimethylphenyl)-n-(4-ethoxy-2-methylbutan-2-yl)acetamide Chemical compound CCOCCC(C)(C)N(C(=O)CCl)C1=C(C)C=CC=C1C NZKNDSNFQUHUDF-UHFFFAOYSA-N 0.000 claims description 2
- XZSLOQBJJCONRW-UHFFFAOYSA-N 2-chloro-n-(2-ethoxyethyl)-n-(2-ethyl-6-methylphenyl)acetamide Chemical compound CCOCCN(C(=O)CCl)C1=C(C)C=CC=C1CC XZSLOQBJJCONRW-UHFFFAOYSA-N 0.000 claims description 2
- WTDMSARUTWSAFQ-UHFFFAOYSA-N 2-chloro-n-(2-ethoxyethyl)-n-(2-methylphenyl)acetamide Chemical compound CCOCCN(C(=O)CCl)C1=CC=CC=C1C WTDMSARUTWSAFQ-UHFFFAOYSA-N 0.000 claims description 2
- XXBNWSRSCPMELR-UHFFFAOYSA-N 2-chloro-n-(2-ethyl-6-methylphenyl)-n-(2-methoxyethyl)acetamide Chemical compound CCC1=CC=CC(C)=C1N(CCOC)C(=O)CCl XXBNWSRSCPMELR-UHFFFAOYSA-N 0.000 claims description 2
- CSDFLGOLPKXOBC-UHFFFAOYSA-N 2-chloro-n-(2-ethyl-6-methylphenyl)-n-(2-propan-2-yloxyethyl)acetamide Chemical compound CCC1=CC=CC(C)=C1N(CCOC(C)C)C(=O)CCl CSDFLGOLPKXOBC-UHFFFAOYSA-N 0.000 claims description 2
- GMDBXHNSCSJZLE-UHFFFAOYSA-N 2-chloro-n-(2-ethyl-6-methylphenyl)-n-(2-propoxyethyl)acetamide Chemical compound CCCOCCN(C(=O)CCl)C1=C(C)C=CC=C1CC GMDBXHNSCSJZLE-UHFFFAOYSA-N 0.000 claims description 2
- SXAAVRUIADQETA-UHFFFAOYSA-N 2-chloro-n-(2-methoxyethyl)-n-(2-methylphenyl)acetamide Chemical compound COCCN(C(=O)CCl)C1=CC=CC=C1C SXAAVRUIADQETA-UHFFFAOYSA-N 0.000 claims description 2
- AEKGSQRXZIDNMI-UHFFFAOYSA-N 2-chloro-n-(cyclohexen-1-yl)-n-propan-2-ylacetamide Chemical compound ClCC(=O)N(C(C)C)C1=CCCCC1 AEKGSQRXZIDNMI-UHFFFAOYSA-N 0.000 claims description 2
- ZMFVLNREWBABDO-UHFFFAOYSA-N 2-chloro-n-propan-2-yl-n-(3,3,5,5-tetramethylcyclohexen-1-yl)acetamide Chemical compound ClCC(=O)N(C(C)C)C1=CC(C)(C)CC(C)(C)C1 ZMFVLNREWBABDO-UHFFFAOYSA-N 0.000 claims description 2
- VTNQPKFIQCLBDU-UHFFFAOYSA-N Acetochlor Chemical compound CCOCN(C(=O)CCl)C1=C(C)C=CC=C1CC VTNQPKFIQCLBDU-UHFFFAOYSA-N 0.000 claims description 2
- 239000005508 Dimethachlor Substances 0.000 claims description 2
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 claims description 2
- 239000004952 Polyamide Substances 0.000 claims description 2
- YLPGTOIOYRQOHV-UHFFFAOYSA-N Pretilachlor Chemical compound CCCOCCN(C(=O)CCl)C1=C(CC)C=CC=C1CC YLPGTOIOYRQOHV-UHFFFAOYSA-N 0.000 claims description 2
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 claims description 2
- 150000004945 aromatic hydrocarbons Chemical class 0.000 claims description 2
- HKPHPIREJKHECO-UHFFFAOYSA-N butachlor Chemical compound CCCCOCN(C(=O)CCl)C1=C(CC)C=CC=C1CC HKPHPIREJKHECO-UHFFFAOYSA-N 0.000 claims description 2
- 239000006184 cosolvent Substances 0.000 claims description 2
- 150000003997 cyclic ketones Chemical class 0.000 claims description 2
- 229910052736 halogen Inorganic materials 0.000 claims description 2
- 150000002367 halogens Chemical class 0.000 claims description 2
- WMRNUXKJMBLTLO-UHFFFAOYSA-N n-(2-butoxyethyl)-2-chloro-n-(2,6-diethylphenyl)acetamide Chemical compound CCCCOCCN(C(=O)CCl)C1=C(CC)C=CC=C1CC WMRNUXKJMBLTLO-UHFFFAOYSA-N 0.000 claims description 2
- 229920002647 polyamide Polymers 0.000 claims description 2
- 239000008096 xylene Substances 0.000 claims description 2
- WNFVVJKAQZVPBK-UHFFFAOYSA-N 2-chloro-n-(2,6-diethylphenyl)-n-(2-ethoxyethyl)acetamide Chemical compound CCOCCN(C(=O)CCl)C1=C(CC)C=CC=C1CC WNFVVJKAQZVPBK-UHFFFAOYSA-N 0.000 claims 1
- HJMQOYUROLIRKV-UHFFFAOYSA-N 2-chloro-n-(2-chloro-6-methylphenyl)-n-(2-methoxyethyl)acetamide Chemical compound COCCN(C(=O)CCl)C1=C(C)C=CC=C1Cl HJMQOYUROLIRKV-UHFFFAOYSA-N 0.000 claims 1
- 150000008282 halocarbons Chemical class 0.000 claims 1
- 239000003350 kerosene Substances 0.000 claims 1
- 230000008635 plant growth Effects 0.000 claims 1
- 230000000379 polymerizing effect Effects 0.000 claims 1
- LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 claims 1
- 238000003756 stirring Methods 0.000 description 70
- 239000000243 solution Substances 0.000 description 51
- NAQMVNRVTILPCV-UHFFFAOYSA-N hexane-1,6-diamine Chemical compound NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 description 50
- 239000002270 dispersing agent Substances 0.000 description 42
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 38
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 30
- UPMLOUAZCHDJJD-UHFFFAOYSA-N 4,4'-Diphenylmethane Diisocyanate Chemical compound C1=CC(N=C=O)=CC=C1CC1=CC=C(N=C=O)C=C1 UPMLOUAZCHDJJD-UHFFFAOYSA-N 0.000 description 29
- 239000007864 aqueous solution Substances 0.000 description 29
- RVGRUAULSDPKGF-UHFFFAOYSA-N Poloxamer Chemical compound C1CO1.CC1CO1 RVGRUAULSDPKGF-UHFFFAOYSA-N 0.000 description 24
- -1 l~o-propyl Chemical group 0.000 description 18
- 239000000047 product Substances 0.000 description 18
- 239000002253 acid Substances 0.000 description 17
- 125000000129 anionic group Chemical group 0.000 description 17
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 16
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 16
- 150000001412 amines Chemical class 0.000 description 13
- 239000008367 deionised water Substances 0.000 description 13
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 12
- 238000006243 chemical reaction Methods 0.000 description 12
- 238000009472 formulation Methods 0.000 description 12
- 239000002245 particle Substances 0.000 description 12
- 239000011541 reaction mixture Substances 0.000 description 12
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 10
- 239000000725 suspension Substances 0.000 description 10
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 description 9
- 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 9
- 239000002736 nonionic surfactant Substances 0.000 description 9
- 150000003839 salts Chemical class 0.000 description 9
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 8
- 230000015572 biosynthetic process Effects 0.000 description 8
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 8
- 150000002170 ethers Chemical class 0.000 description 8
- 230000007774 longterm Effects 0.000 description 8
- 125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 description 8
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 7
- 230000000977 initiatory effect Effects 0.000 description 7
- 150000003254 radicals Chemical class 0.000 description 7
- WHOZNOZYMBRCBL-OUKQBFOZSA-N (2E)-2-Tetradecenal Chemical compound CCCCCCCCCCC\C=C\C=O WHOZNOZYMBRCBL-OUKQBFOZSA-N 0.000 description 6
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 6
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 6
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 6
- 239000004480 active ingredient Substances 0.000 description 6
- 239000013543 active substance Substances 0.000 description 6
- 229940012017 ethylenediamine Drugs 0.000 description 6
- 229940044654 phenolsulfonic acid Drugs 0.000 description 6
- 239000002202 Polyethylene glycol Substances 0.000 description 5
- 150000003863 ammonium salts Chemical class 0.000 description 5
- 239000002585 base Substances 0.000 description 5
- 235000014113 dietary fatty acids Nutrition 0.000 description 5
- 230000000694 effects Effects 0.000 description 5
- 239000004495 emulsifiable concentrate Substances 0.000 description 5
- 239000000194 fatty acid Substances 0.000 description 5
- 229930195729 fatty acid Natural products 0.000 description 5
- 239000012948 isocyanate Substances 0.000 description 5
- 229920001223 polyethylene glycol Polymers 0.000 description 5
- 229920002451 polyvinyl alcohol Polymers 0.000 description 5
- 230000001681 protective effect Effects 0.000 description 5
- 239000002689 soil Substances 0.000 description 5
- 239000000126 substance Substances 0.000 description 5
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical group 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 4
- 239000005639 Lauric acid Substances 0.000 description 4
- 125000001931 aliphatic group Chemical group 0.000 description 4
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 4
- 150000001342 alkaline earth metals Chemical class 0.000 description 4
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 4
- 239000000084 colloidal system Substances 0.000 description 4
- 125000005442 diisocyanate group Chemical group 0.000 description 4
- IPCSVZSSVZVIGE-UHFFFAOYSA-N hexadecanoic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 4
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 4
- 235000019422 polyvinyl alcohol Nutrition 0.000 description 4
- 229910052708 sodium Inorganic materials 0.000 description 4
- 239000011734 sodium Substances 0.000 description 4
- 239000007787 solid Substances 0.000 description 4
- 238000006277 sulfonation reaction Methods 0.000 description 4
- 229920003169 water-soluble polymer Polymers 0.000 description 4
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 3
- QFMDFTQOJHFVNR-UHFFFAOYSA-N 1-[2,2-dichloro-1-(4-ethylphenyl)ethyl]-4-ethylbenzene Chemical compound C1=CC(CC)=CC=C1C(C(Cl)Cl)C1=CC=C(CC)C=C1 QFMDFTQOJHFVNR-UHFFFAOYSA-N 0.000 description 3
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 3
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical group [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 3
- 239000005642 Oleic acid Substances 0.000 description 3
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 3
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 3
- 239000004372 Polyvinyl alcohol Substances 0.000 description 3
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical group [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 235000021355 Stearic acid Nutrition 0.000 description 3
- 229910052783 alkali metal Inorganic materials 0.000 description 3
- 150000001340 alkali metals Chemical class 0.000 description 3
- 125000003277 amino group Chemical group 0.000 description 3
- 125000003118 aryl group Chemical group 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 150000004985 diamines Chemical class 0.000 description 3
- 150000004665 fatty acids Chemical class 0.000 description 3
- 239000011521 glass Substances 0.000 description 3
- 150000002513 isocyanates Chemical class 0.000 description 3
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 3
- HJOVHMDZYOCNQW-UHFFFAOYSA-N isophorone Chemical compound CC1=CC(=O)CC(C)(C)C1 HJOVHMDZYOCNQW-UHFFFAOYSA-N 0.000 description 3
- 239000011777 magnesium Chemical group 0.000 description 3
- 229910052749 magnesium Inorganic materials 0.000 description 3
- 239000000178 monomer Substances 0.000 description 3
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 3
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 3
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 3
- 229920001983 poloxamer Polymers 0.000 description 3
- 239000011591 potassium Chemical group 0.000 description 3
- 229910052700 potassium Inorganic materials 0.000 description 3
- 229960004063 propylene glycol Drugs 0.000 description 3
- 238000007127 saponification reaction Methods 0.000 description 3
- 239000008117 stearic acid Substances 0.000 description 3
- 150000005846 sugar alcohols Polymers 0.000 description 3
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Classifications
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- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/18—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing the group —CO—N<, e.g. carboxylic acid amides or imides; Thio analogues 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
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/18—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing the group —CO—N<, e.g. carboxylic acid amides or imides; Thio analogues thereof
- A01N37/22—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing the group —CO—N<, e.g. carboxylic acid amides or imides; Thio analogues thereof the nitrogen atom being directly attached to an aromatic ring system, e.g. anilides
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/18—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing the group —CO—N<, e.g. carboxylic acid amides or imides; Thio analogues thereof
- A01N37/26—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing the group —CO—N<, e.g. carboxylic acid amides or imides; Thio analogues thereof containing the group; Thio analogues thereof
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH84987 | 1987-03-06 | ||
| CH849/87-6 | 1987-03-06 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA1311937C true CA1311937C (en) | 1992-12-29 |
Family
ID=4196639
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA000560536A Expired - Lifetime CA1311937C (en) | 1987-03-06 | 1988-03-04 | Herbicidal compositions |
Country Status (14)
| Country | Link |
|---|---|
| US (1) | US5006161A (enExample) |
| EP (1) | EP0281521B1 (enExample) |
| JP (1) | JPS63230606A (enExample) |
| AT (1) | ATE77917T1 (enExample) |
| AU (1) | AU607192B2 (enExample) |
| BR (1) | BR8800962A (enExample) |
| CA (1) | CA1311937C (enExample) |
| DE (1) | DE3872547D1 (enExample) |
| ES (1) | ES2042794T3 (enExample) |
| GR (1) | GR3005136T3 (enExample) |
| HU (1) | HU204395B (enExample) |
| IL (1) | IL85626A (enExample) |
| YU (1) | YU43488A (enExample) |
| ZA (1) | ZA881552B (enExample) |
Families Citing this family (21)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JO1588B1 (en) * | 1988-09-02 | 1989-12-16 | سيبا جيجي ايه جي | Mixture or a mixture of aprons |
| DK0570382T3 (da) * | 1991-02-06 | 1999-09-27 | Zeneca Ag Products Inc | Mikroindkapslet, herbicid sammensætning |
| ATE167980T1 (de) * | 1993-11-15 | 1998-07-15 | Zeneca Ltd | Mikrokapseln, die suspensionen von biologisch aktiven verbindungen enthalten |
| AU734106B2 (en) * | 1994-11-16 | 2001-06-07 | Fmc Corporation | Low volatility formulations of clomazone |
| WO1996014743A1 (en) * | 1994-11-16 | 1996-05-23 | Fmc Corporation | Low volatility formulations of clomazone |
| US5597780A (en) * | 1994-11-16 | 1997-01-28 | Fmc Corporation | Low volatility formulations of microencapsulated clomazone |
| US5993842A (en) * | 1994-12-12 | 1999-11-30 | Zeneca Limited | Microcapsules containing suspensions of biologically active compounds |
| US6992047B2 (en) * | 2001-04-11 | 2006-01-31 | Monsanto Technology Llc | Method of microencapsulating an agricultural active having a high melting point and uses for such materials |
| WO2004054362A1 (en) * | 2002-12-13 | 2004-07-01 | Monsanto Technology Llc | Microcapsules with amine adjusted release rates |
| WO2005122758A1 (en) * | 2004-06-14 | 2005-12-29 | Monsanto Technology Llc | Microcapsules having activated release of core material therein |
| DE602004023622D1 (de) * | 2004-11-26 | 2009-11-26 | Swatch Group Man Serv Ag | Uhr mit verwechselbarer Lunette |
| US20070185003A1 (en) * | 2006-01-18 | 2007-08-09 | Invista North America S.A.R.L. | Non-textile polymer compositions and methods |
| BRPI0706934A2 (pt) * | 2006-01-18 | 2011-04-19 | Invista Technologies S A R L Empr Luxemburguesa | composição de cuidado do tecido, composições , pó de poliuretanouréia, método para a extensão da concretização do perfume em um tecido, método de aumento da retenção do formato da vestimenta, método para aumentar a facilidade das propriedades de cuidado de um tecido, método para proporcionar propriedade anti-manchas a um tecido, métodos para a preparação do pó de poliuretanouréia, método para o tingimento de uma composição em pó e método para prolongar a concretização do perfume em uma composição |
| PL2395843T3 (pl) * | 2009-02-13 | 2018-01-31 | Monsanto Technology Llc | Kapsułkowanie herbicydów do zmniejszenia uszkodzeń upraw |
| PL2605646T3 (pl) | 2010-08-18 | 2017-01-31 | Monsanto Technology Llc | Wczesne zastosowanie kapsułkowych pochodnych acetamidu w celu zmniejszenia uszkodzeń upraw |
| BR102012027933A2 (pt) | 2011-11-01 | 2015-11-17 | Dow Agrosciences Llc | composições pesticidas estáveis |
| RU2628579C2 (ru) | 2012-07-27 | 2017-08-21 | Фмк Корпорейшн | Составы кломазона |
| MX383040B (es) | 2014-01-27 | 2025-03-13 | Monsanto Technology Llc | Concentrados herbicidas acuosos. |
| US9661846B2 (en) * | 2014-09-08 | 2017-05-30 | Upl Limited | Agrochemical compositions |
| MX2019015014A (es) | 2017-06-13 | 2020-02-26 | Monsanto Technology Llc | Herbicidas microencapsulados. |
| UA129154C2 (uk) | 2019-01-30 | 2025-01-29 | Монсанто Текнолоджі Ллс | Мікрокапсульовані ацетамідні гербіциди |
Family Cites Families (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4285720A (en) * | 1972-03-15 | 1981-08-25 | Stauffer Chemical Company | Encapsulation process and capsules produced thereby |
| US4160838A (en) * | 1977-06-02 | 1979-07-10 | Janssen Pharmaceutica N.V. | Antimicrobial and plant-growth-regulating triazole derivatives |
| DE2757017C3 (de) * | 1977-12-21 | 1986-07-31 | Hoechst Ag, 6230 Frankfurt | Verfahren zum Herstellen von druckbeständigen Polyurethan-Polyharnstoff-Kapseln mit strukturierter Innenmasse |
| US4351667A (en) * | 1978-04-18 | 1982-09-28 | Monsanto Company | Herbicidal tertiary 2-haloacetamides |
| JPS558856A (en) * | 1978-07-05 | 1980-01-22 | Mitsubishi Paper Mills Ltd | Covering of finely dispersed liquid droplet with thin film |
| TR20508A (tr) * | 1978-12-29 | 1981-09-03 | Ruhr Stickstoff Ag | Ikameli n-(trimetil-sikloalkenil)n-alkilasetamid'ler ve bunlarin fitatoksik mamullerde kullanilmalari |
| DE3245020A1 (de) * | 1982-12-06 | 1984-06-07 | Celamerck Gmbh & Co Kg, 6507 Ingelheim | Cycloalkenylderivate, ihre herstellung und verwendung |
| US4563212A (en) * | 1983-12-27 | 1986-01-07 | Monsanto Company | High concentration encapsulation by interfacial polycondensation |
| US4640709A (en) * | 1984-06-12 | 1987-02-03 | Monsanto Company | High concentration encapsulation by interfacial polycondensation |
| ATE77916T1 (de) * | 1985-09-13 | 1992-07-15 | Ciba Geigy Ag | Verfahren zur herstellung von mikrokapseln. |
-
1988
- 1988-02-29 EP EP88810125A patent/EP0281521B1/de not_active Expired - Lifetime
- 1988-02-29 ES ES88810125T patent/ES2042794T3/es not_active Expired - Lifetime
- 1988-02-29 DE DE8888810125T patent/DE3872547D1/de not_active Expired - Lifetime
- 1988-02-29 AT AT88810125T patent/ATE77917T1/de not_active IP Right Cessation
- 1988-03-01 US US07/162,534 patent/US5006161A/en not_active Expired - Fee Related
- 1988-03-03 IL IL85626A patent/IL85626A/xx not_active IP Right Cessation
- 1988-03-03 YU YU00434/88A patent/YU43488A/xx unknown
- 1988-03-04 ZA ZA881552A patent/ZA881552B/xx unknown
- 1988-03-04 AU AU12720/88A patent/AU607192B2/en not_active Ceased
- 1988-03-04 HU HU881080A patent/HU204395B/hu not_active IP Right Cessation
- 1988-03-04 BR BR8800962A patent/BR8800962A/pt active Search and Examination
- 1988-03-04 CA CA000560536A patent/CA1311937C/en not_active Expired - Lifetime
- 1988-03-07 JP JP63053427A patent/JPS63230606A/ja active Pending
-
1992
- 1992-07-10 GR GR920401366T patent/GR3005136T3/el unknown
Also Published As
| Publication number | Publication date |
|---|---|
| ES2042794T3 (es) | 1993-12-16 |
| IL85626A (en) | 1992-08-18 |
| HUT48803A (en) | 1989-07-28 |
| YU43488A (en) | 1989-10-31 |
| AU607192B2 (en) | 1991-02-28 |
| BR8800962A (pt) | 1988-10-11 |
| EP0281521A2 (de) | 1988-09-07 |
| ZA881552B (en) | 1990-03-28 |
| EP0281521A3 (en) | 1990-09-19 |
| EP0281521B1 (de) | 1992-07-08 |
| GR3005136T3 (enExample) | 1993-05-24 |
| JPS63230606A (ja) | 1988-09-27 |
| ATE77917T1 (de) | 1992-07-15 |
| HU204395B (en) | 1992-01-28 |
| US5006161A (en) | 1991-04-09 |
| DE3872547D1 (de) | 1992-08-13 |
| AU1272088A (en) | 1988-09-08 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| MKLA | Lapsed |