UA76455C2 - Process of gelatinization, a water herbicidal composition (variants), a process of preparation the composition and a method to control undesired vegetation - Google Patents
Process of gelatinization, a water herbicidal composition (variants), a process of preparation the composition and a method to control undesired vegetation Download PDFInfo
- Publication number
- UA76455C2 UA76455C2 UA2003109606A UA2003109606A UA76455C2 UA 76455 C2 UA76455 C2 UA 76455C2 UA 2003109606 A UA2003109606 A UA 2003109606A UA 2003109606 A UA2003109606 A UA 2003109606A UA 76455 C2 UA76455 C2 UA 76455C2
- Authority
- UA
- Ukraine
- Prior art keywords
- composition according
- aqueous composition
- composition
- alginate
- salt
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 222
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 title claims abstract description 22
- 230000002363 herbicidal effect Effects 0.000 title claims description 28
- 238000000034 method Methods 0.000 title claims description 12
- 238000002360 preparation method Methods 0.000 title description 4
- 230000008569 process Effects 0.000 title description 3
- 235000010443 alginic acid Nutrition 0.000 claims abstract description 54
- 229920000615 alginic acid Polymers 0.000 claims abstract description 54
- FHVDTGUDJYJELY-UHFFFAOYSA-N 6-{[2-carboxy-4,5-dihydroxy-6-(phosphanyloxy)oxan-3-yl]oxy}-4,5-dihydroxy-3-phosphanyloxane-2-carboxylic acid Chemical compound O1C(C(O)=O)C(P)C(O)C(O)C1OC1C(C(O)=O)OC(OP)C(O)C1O FHVDTGUDJYJELY-UHFFFAOYSA-N 0.000 claims abstract description 42
- 229940072056 alginate Drugs 0.000 claims abstract description 42
- 239000002895 emetic Substances 0.000 claims abstract description 36
- 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 claims abstract description 24
- SYJFEGQWDCRVNX-UHFFFAOYSA-N diquat Chemical compound C1=CC=[N+]2CC[N+]3=CC=CC=C3C2=C1 SYJFEGQWDCRVNX-UHFFFAOYSA-N 0.000 claims abstract description 20
- 239000008141 laxative Substances 0.000 claims abstract description 19
- 230000000694 effects Effects 0.000 claims abstract description 16
- 210000004051 gastric juice Anatomy 0.000 claims abstract description 11
- 150000003839 salts Chemical class 0.000 claims abstract description 9
- 239000003349 gelling agent Substances 0.000 claims abstract description 8
- 239000003795 chemical substances by application Substances 0.000 claims description 23
- 230000002475 laxative effect Effects 0.000 claims description 18
- 239000000243 solution Substances 0.000 claims description 17
- 239000004094 surface-active agent Substances 0.000 claims description 14
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 claims description 12
- 230000015572 biosynthetic process Effects 0.000 claims description 12
- 239000007787 solid Substances 0.000 claims description 10
- 230000002378 acidificating effect Effects 0.000 claims description 9
- 150000003973 alkyl amines Chemical class 0.000 claims description 9
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 claims description 8
- 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 claims description 8
- 125000000129 anionic group Chemical group 0.000 claims description 8
- 239000011575 calcium Substances 0.000 claims description 8
- 229910052791 calcium Inorganic materials 0.000 claims description 8
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- 239000003945 anionic surfactant Substances 0.000 claims description 6
- 239000003093 cationic surfactant Substances 0.000 claims description 6
- 150000002500 ions Chemical class 0.000 claims description 6
- 229910052943 magnesium sulfate Inorganic materials 0.000 claims description 6
- 235000019341 magnesium sulphate Nutrition 0.000 claims description 6
- 239000002736 nonionic surfactant Substances 0.000 claims description 6
- 229920002451 polyvinyl alcohol Polymers 0.000 claims description 6
- QXNVGIXVLWOKEQ-UHFFFAOYSA-N Disodium Chemical compound [Na][Na] QXNVGIXVLWOKEQ-UHFFFAOYSA-N 0.000 claims description 5
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 claims description 5
- 125000002091 cationic group Chemical group 0.000 claims description 5
- 229920000642 polymer Polymers 0.000 claims description 5
- 229920005682 EO-PO block copolymer Polymers 0.000 claims description 4
- 150000001298 alcohols Chemical class 0.000 claims description 4
- 238000002156 mixing Methods 0.000 claims description 4
- 239000002202 Polyethylene glycol Substances 0.000 claims description 3
- CZPWVGJYEJSRLH-UHFFFAOYSA-N Pyrimidine Chemical compound C1=CN=CN=C1 CZPWVGJYEJSRLH-UHFFFAOYSA-N 0.000 claims description 3
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- 239000007864 aqueous solution Substances 0.000 claims description 3
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- 235000014113 dietary fatty acids Nutrition 0.000 claims description 3
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- 229930195729 fatty acid Natural products 0.000 claims description 3
- 150000004665 fatty acids Chemical class 0.000 claims description 3
- CSRCNKZJIYKJOT-UHFFFAOYSA-N formaldehyde;naphthalene;sodium Chemical compound [Na].O=C.C1=CC=CC2=CC=CC=C21 CSRCNKZJIYKJOT-UHFFFAOYSA-N 0.000 claims description 3
- 229920000847 nonoxynol Polymers 0.000 claims description 3
- 239000001814 pectin Substances 0.000 claims description 3
- 229920001277 pectin Polymers 0.000 claims description 3
- 235000010987 pectin Nutrition 0.000 claims description 3
- 229920001223 polyethylene glycol Polymers 0.000 claims description 3
- IZWPGJFSBABFGL-GMFCBQQYSA-M sodium;2-[methyl-[(z)-octadec-9-enoyl]amino]ethanesulfonate Chemical compound [Na+].CCCCCCCC\C=C/CCCCCCCC(=O)N(C)CCS([O-])(=O)=O IZWPGJFSBABFGL-GMFCBQQYSA-M 0.000 claims description 3
- 239000000126 substance Substances 0.000 claims description 3
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 claims description 2
- 239000011777 magnesium Substances 0.000 claims description 2
- 229910052749 magnesium Inorganic materials 0.000 claims description 2
- 150000001735 carboxylic acids Chemical class 0.000 claims 2
- 150000002148 esters Chemical class 0.000 claims 2
- 150000003014 phosphoric acid esters Chemical class 0.000 claims 2
- 239000013543 active substance Substances 0.000 claims 1
- 235000010410 calcium alginate Nutrition 0.000 claims 1
- 239000000648 calcium alginate Substances 0.000 claims 1
- 229960002681 calcium alginate Drugs 0.000 claims 1
- OKHHGHGGPDJQHR-YMOPUZKJSA-L calcium;(2s,3s,4s,5s,6r)-6-[(2r,3s,4r,5s,6r)-2-carboxy-6-[(2r,3s,4r,5s,6r)-2-carboxylato-4,5,6-trihydroxyoxan-3-yl]oxy-4,5-dihydroxyoxan-3-yl]oxy-3,4,5-trihydroxyoxane-2-carboxylate Chemical compound [Ca+2].O[C@@H]1[C@H](O)[C@H](O)O[C@@H](C([O-])=O)[C@H]1O[C@H]1[C@@H](O)[C@@H](O)[C@H](O[C@H]2[C@H]([C@@H](O)[C@H](O)[C@H](O2)C([O-])=O)O)[C@H](C(O)=O)O1 OKHHGHGGPDJQHR-YMOPUZKJSA-L 0.000 claims 1
- GXGAKHNRMVGRPK-UHFFFAOYSA-N dimagnesium;dioxido-bis[[oxido(oxo)silyl]oxy]silane Chemical compound [Mg+2].[Mg+2].[O-][Si](=O)O[Si]([O-])([O-])O[Si]([O-])=O GXGAKHNRMVGRPK-UHFFFAOYSA-N 0.000 abstract description 12
- 239000000391 magnesium silicate Substances 0.000 abstract description 12
- 229940099273 magnesium trisilicate Drugs 0.000 abstract description 12
- 229910000386 magnesium trisilicate Inorganic materials 0.000 abstract description 12
- 235000019793 magnesium trisilicate Nutrition 0.000 abstract description 12
- 239000005630 Diquat Substances 0.000 abstract description 8
- 239000002253 acid Substances 0.000 abstract description 2
- 238000004519 manufacturing process Methods 0.000 abstract description 2
- 230000001960 triggered effect Effects 0.000 abstract 2
- 230000001543 purgative effect Effects 0.000 abstract 1
- -1 phosphate ester Chemical class 0.000 description 17
- 239000004009 herbicide Substances 0.000 description 14
- ROFVEXUMMXZLPA-UHFFFAOYSA-N Bipyridyl Chemical group N1=CC=CC=C1C1=CC=CC=N1 ROFVEXUMMXZLPA-UHFFFAOYSA-N 0.000 description 13
- 239000002131 composite material Substances 0.000 description 10
- 150000001450 anions Chemical class 0.000 description 8
- 238000010521 absorption reaction Methods 0.000 description 7
- 239000000375 suspending agent Substances 0.000 description 7
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 6
- 150000001768 cations Chemical class 0.000 description 6
- 150000001875 compounds Chemical class 0.000 description 6
- 230000001681 protective effect Effects 0.000 description 6
- 210000002784 stomach Anatomy 0.000 description 6
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- 238000003860 storage Methods 0.000 description 5
- 230000001965 increasing effect Effects 0.000 description 4
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- 230000008673 vomiting Effects 0.000 description 4
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
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- 230000007935 neutral effect Effects 0.000 description 3
- INFDPOAKFNIJBF-UHFFFAOYSA-N paraquat Chemical group C1=C[N+](C)=CC=C1C1=CC=[N+](C)C=C1 INFDPOAKFNIJBF-UHFFFAOYSA-N 0.000 description 3
- 210000000813 small intestine Anatomy 0.000 description 3
- 241000894007 species Species 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
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- 241000283973 Oryctolagus cuniculus Species 0.000 description 2
- 229910019142 PO4 Inorganic materials 0.000 description 2
- UPWPBIUUSLIWAI-UHFFFAOYSA-N [4-(4-aminophenyl)sulfonylphenyl]urea Chemical compound C1=CC(NC(=O)N)=CC=C1S(=O)(=O)C1=CC=C(N)C=C1 UPWPBIUUSLIWAI-UHFFFAOYSA-N 0.000 description 2
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- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 2
- XEJNEDVTJPXRSM-UHFFFAOYSA-N 1-(2,4-dichlorophenyl)-5-methyl-4,5-dihydro-1H-pyrazole-3,5-dicarboxylic acid Chemical compound OC(=O)C1(C)CC(C(O)=O)=NN1C1=CC=C(Cl)C=C1Cl XEJNEDVTJPXRSM-UHFFFAOYSA-N 0.000 description 1
- BXKKQFGRMSOANI-UHFFFAOYSA-N 1-methoxy-3-[4-[(2-methoxy-2,4,4-trimethyl-3h-chromen-7-yl)oxy]phenyl]-1-methylurea Chemical compound C1=CC(NC(=O)N(C)OC)=CC=C1OC1=CC=C2C(C)(C)CC(C)(OC)OC2=C1 BXKKQFGRMSOANI-UHFFFAOYSA-N 0.000 description 1
- MCNOFYBITGAAGM-UHFFFAOYSA-N 2,2-dichloro-1-[5-(furan-2-yl)-2,2-dimethyl-1,3-oxazolidin-3-yl]ethanone Chemical compound C1N(C(=O)C(Cl)Cl)C(C)(C)OC1C1=CC=CO1 MCNOFYBITGAAGM-UHFFFAOYSA-N 0.000 description 1
- NUPJIGQFXCQJBK-UHFFFAOYSA-N 2-(4-isopropyl-4-methyl-5-oxo-4,5-dihydro-1H-imidazol-2-yl)-5-(methoxymethyl)nicotinic acid Chemical compound OC(=O)C1=CC(COC)=CN=C1C1=NC(C)(C(C)C)C(=O)N1 NUPJIGQFXCQJBK-UHFFFAOYSA-N 0.000 description 1
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- CABMTIJINOIHOD-UHFFFAOYSA-N 2-[4-methyl-5-oxo-4-(propan-2-yl)-4,5-dihydro-1H-imidazol-2-yl]quinoline-3-carboxylic acid Chemical compound N1C(=O)C(C(C)C)(C)N=C1C1=NC2=CC=CC=C2C=C1C(O)=O CABMTIJINOIHOD-UHFFFAOYSA-N 0.000 description 1
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- ULUAUXLGCMPNKK-UHFFFAOYSA-N Sulfobutanedioic acid Chemical class OC(=O)CC(C(O)=O)S(O)(=O)=O ULUAUXLGCMPNKK-UHFFFAOYSA-N 0.000 description 1
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- ZCNQYNHDVRPZIH-UHFFFAOYSA-N fluthiacet-methyl Chemical group C1=C(Cl)C(SCC(=O)OC)=CC(N=C2N3CCCCN3C(=O)S2)=C1F ZCNQYNHDVRPZIH-UHFFFAOYSA-N 0.000 description 1
- 230000037406 food intake Effects 0.000 description 1
- PXDNXJSDGQBLKS-UHFFFAOYSA-N foramsulfuron Chemical compound COC1=CC(OC)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=C(NC=O)C=2)C(=O)N(C)C)=N1 PXDNXJSDGQBLKS-UHFFFAOYSA-N 0.000 description 1
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- VZCYOOQTPOCHFL-OWOJBTEDSA-L fumarate(2-) Chemical compound [O-]C(=O)\C=C\C([O-])=O VZCYOOQTPOCHFL-OWOJBTEDSA-L 0.000 description 1
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- NPUOZEMYDHAAMG-UHFFFAOYSA-N hexamagnesium;trisilicate Chemical group [Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-] NPUOZEMYDHAAMG-UHFFFAOYSA-N 0.000 description 1
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 1
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- KEBHLNDPKPIPLI-UHFFFAOYSA-N hydron;2-(3h-inden-4-yloxymethyl)morpholine;chloride Chemical compound Cl.C=1C=CC=2C=CCC=2C=1OCC1CNCCO1 KEBHLNDPKPIPLI-UHFFFAOYSA-N 0.000 description 1
- RUCAXVJJQQJZGU-UHFFFAOYSA-M hydron;2-(phosphonatomethylamino)acetate;trimethylsulfanium Chemical compound C[S+](C)C.OP(O)(=O)CNCC([O-])=O RUCAXVJJQQJZGU-UHFFFAOYSA-M 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 230000000968 intestinal effect Effects 0.000 description 1
- 239000011344 liquid material Substances 0.000 description 1
- OQXSVLMHUIVNRJ-UHFFFAOYSA-L magnesium;2-dodecylbenzenesulfonate Chemical compound [Mg+2].CCCCCCCCCCCCC1=CC=CC=C1S([O-])(=O)=O.CCCCCCCCCCCCC1=CC=CC=C1S([O-])(=O)=O OQXSVLMHUIVNRJ-UHFFFAOYSA-L 0.000 description 1
- 229940049920 malate Drugs 0.000 description 1
- BJEPYKJPYRNKOW-UHFFFAOYSA-L malate(2-) Chemical compound [O-]C(=O)C(O)CC([O-])=O BJEPYKJPYRNKOW-UHFFFAOYSA-L 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
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- JZMJDSHXVKJFKW-UHFFFAOYSA-M methyl sulfate(1-) Chemical compound COS([O-])(=O)=O JZMJDSHXVKJFKW-UHFFFAOYSA-M 0.000 description 1
- FOXFZRUHNHCZPX-UHFFFAOYSA-N metribuzin Chemical compound CSC1=NN=C(C(C)(C)C)C(=O)N1N FOXFZRUHNHCZPX-UHFFFAOYSA-N 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 210000004400 mucous membrane Anatomy 0.000 description 1
- RTCOGUMHFFWOJV-UHFFFAOYSA-N nicosulfuron Chemical compound COC1=CC(OC)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CN=2)C(=O)N(C)C)=N1 RTCOGUMHFFWOJV-UHFFFAOYSA-N 0.000 description 1
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- 239000001301 oxygen Substances 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- CHIFOSRWCNZCFN-UHFFFAOYSA-N pendimethalin Chemical compound CCC(CC)NC1=C([N+]([O-])=O)C=C(C)C(C)=C1[N+]([O-])=O CHIFOSRWCNZCFN-UHFFFAOYSA-N 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 239000012071 phase Substances 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 150000003222 pyridines Chemical class 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 230000011514 reflex Effects 0.000 description 1
- MEFOUWRMVYJCQC-UHFFFAOYSA-N rimsulfuron Chemical compound CCS(=O)(=O)C1=CC=CN=C1S(=O)(=O)NC(=O)NC1=NC(OC)=CC(OC)=N1 MEFOUWRMVYJCQC-UHFFFAOYSA-N 0.000 description 1
- 238000004062 sedimentation Methods 0.000 description 1
- 238000005204 segregation Methods 0.000 description 1
- 230000035939 shock Effects 0.000 description 1
- ODCWYMIRDDJXKW-UHFFFAOYSA-N simazine Chemical compound CCNC1=NC(Cl)=NC(NCC)=N1 ODCWYMIRDDJXKW-UHFFFAOYSA-N 0.000 description 1
- WXMKPNITSTVMEF-UHFFFAOYSA-M sodium benzoate Chemical compound [Na+].[O-]C(=O)C1=CC=CC=C1 WXMKPNITSTVMEF-UHFFFAOYSA-M 0.000 description 1
- 239000004299 sodium benzoate Substances 0.000 description 1
- 235000010234 sodium benzoate Nutrition 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-L succinate(2-) Chemical compound [O-]C(=O)CCC([O-])=O KDYFGRWQOYBRFD-UHFFFAOYSA-L 0.000 description 1
- PQTBTIFWAXVEPB-UHFFFAOYSA-N sulcotrione Chemical compound ClC1=CC(S(=O)(=O)C)=CC=C1C(=O)C1C(=O)CCCC1=O PQTBTIFWAXVEPB-UHFFFAOYSA-N 0.000 description 1
- OORLZFUTLGXMEF-UHFFFAOYSA-N sulfentrazone Chemical compound O=C1N(C(F)F)C(C)=NN1C1=CC(NS(C)(=O)=O)=C(Cl)C=C1Cl OORLZFUTLGXMEF-UHFFFAOYSA-N 0.000 description 1
- 210000004243 sweat Anatomy 0.000 description 1
- 230000002195 synergetic effect Effects 0.000 description 1
- 229940095064 tartrate Drugs 0.000 description 1
- IROINLKCQGIITA-UHFFFAOYSA-N terbutryn Chemical compound CCNC1=NC(NC(C)(C)C)=NC(SC)=N1 IROINLKCQGIITA-UHFFFAOYSA-N 0.000 description 1
- FZXISNSWEXTPMF-UHFFFAOYSA-N terbutylazine Chemical compound CCNC1=NC(Cl)=NC(NC(C)(C)C)=N1 FZXISNSWEXTPMF-UHFFFAOYSA-N 0.000 description 1
- LOQQVLXUKHKNIA-UHFFFAOYSA-N thifensulfuron Chemical compound COC1=NC(C)=NC(NC(=O)NS(=O)(=O)C2=C(SC=C2)C(O)=O)=N1 LOQQVLXUKHKNIA-UHFFFAOYSA-N 0.000 description 1
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 1
- KVEQCVKVIFQSGC-UHFFFAOYSA-N tritosulfuron Chemical compound FC(F)(F)C1=NC(OC)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2)C(F)(F)F)=N1 KVEQCVKVIFQSGC-UHFFFAOYSA-N 0.000 description 1
- 229940005605 valeric acid Drugs 0.000 description 1
- 239000011345 viscous material Substances 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 230000003313 weakening effect Effects 0.000 description 1
- 239000000230 xanthan gum Substances 0.000 description 1
- 235000010493 xanthan gum Nutrition 0.000 description 1
- 229920001285 xanthan gum Polymers 0.000 description 1
- 229940082509 xanthan gum Drugs 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
- A01N25/02—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 containing liquids as carriers, diluents or solvents
- A01N25/04—Dispersions, emulsions, suspoemulsions, suspension concentrates or gels
-
- 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
- A01N43/34—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
- A01N43/40—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom six-membered rings
-
- 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
- A01N43/90—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having two or more relevant hetero rings, condensed among themselves or with a common carbocyclic ring system
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Environmental Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (AREA)
- Zoology (AREA)
- Plant Pathology (AREA)
- Chemical & Material Sciences (AREA)
- Dispersion Chemistry (AREA)
- Toxicology (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicinal Preparation (AREA)
- Jellies, Jams, And Syrups (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GBGB0107651.2A GB0107651D0 (en) | 2001-03-27 | 2001-03-27 | Composition |
| PCT/GB2002/001147 WO2002076212A1 (en) | 2001-03-27 | 2002-03-13 | Composition containing paraquat and/or diquat an alginate and an emetic and/or purgative |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| UA76455C2 true UA76455C2 (en) | 2006-08-15 |
Family
ID=9911668
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| UA2003109606A UA76455C2 (en) | 2001-03-27 | 2002-03-13 | Process of gelatinization, a water herbicidal composition (variants), a process of preparation the composition and a method to control undesired vegetation |
Country Status (39)
| Country | Link |
|---|---|
| US (1) | US20040157742A1 (es) |
| EP (1) | EP1383384A1 (es) |
| JP (1) | JP2004524341A (es) |
| KR (1) | KR100552377B1 (es) |
| CN (1) | CN1288975C (es) |
| AP (1) | AP1790A (es) |
| AR (1) | AR033182A1 (es) |
| AU (1) | AU2002242833B2 (es) |
| BG (1) | BG108194A (es) |
| BR (1) | BR0208234A (es) |
| CA (1) | CA2440360A1 (es) |
| CZ (1) | CZ20032577A3 (es) |
| DO (1) | DOP2002000369A (es) |
| EA (1) | EA006169B1 (es) |
| EC (1) | ECSP034777A (es) |
| EE (1) | EE200300461A (es) |
| EG (1) | EG23378A (es) |
| GB (1) | GB0107651D0 (es) |
| GE (1) | GEP20063980B (es) |
| HR (1) | HRP20030779A2 (es) |
| HU (1) | HUP0401309A2 (es) |
| IL (1) | IL158055A0 (es) |
| MA (1) | MA26013A1 (es) |
| MX (1) | MXPA03008621A (es) |
| MY (1) | MY136351A (es) |
| NO (1) | NO20034304L (es) |
| NZ (1) | NZ528116A (es) |
| OA (1) | OA12463A (es) |
| PA (1) | PA8542501A1 (es) |
| PE (1) | PE20020942A1 (es) |
| PL (1) | PL363836A1 (es) |
| SK (1) | SK11902003A3 (es) |
| TN (1) | TNSN03081A1 (es) |
| TW (1) | TWI285531B (es) |
| UA (1) | UA76455C2 (es) |
| UY (1) | UY27229A1 (es) |
| WO (1) | WO2002076212A1 (es) |
| YU (1) | YU74603A (es) |
| ZA (1) | ZA200307170B (es) |
Families Citing this family (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB0301279D0 (en) * | 2003-01-20 | 2003-02-19 | Syngenta Ltd | Method of dermal protection |
| GB0328530D0 (en) * | 2003-12-09 | 2004-01-14 | Syngenta Ltd | Agrochemical composition |
| GB0328529D0 (en) * | 2003-12-09 | 2004-01-14 | Syngenta Ltd | Agrochemical composition |
| GB0328528D0 (en) * | 2003-12-09 | 2004-01-14 | Syngenta Ltd | Agrochemical composition |
| WO2006118562A1 (en) * | 2005-04-29 | 2006-11-09 | Inkine Pharmaceutical Company, Inc. | Purgative composition and uses thereof |
| KR100699672B1 (ko) * | 2005-10-28 | 2007-03-23 | 시논 코포레이션 | 제초제 조성물 |
| SG189757A1 (en) * | 2008-04-08 | 2013-05-31 | Bayer Cropscience Lp | Composition and system for turf maintenance |
| CN102388863B (zh) * | 2011-09-21 | 2014-02-12 | 南京红太阳股份有限公司 | 一种含敌草快二溴盐的水溶性膏剂 |
| CN104365658B (zh) * | 2014-11-06 | 2016-08-17 | 浙江天一农化有限公司 | 一种复配增效除草剂及其制备工艺 |
| US20200128831A1 (en) * | 2017-07-06 | 2020-04-30 | Rhodia Operations | Pesticide Compositions |
| CN113940351A (zh) * | 2020-07-17 | 2022-01-18 | 汕头市深泰新材料科技发展有限公司 | 一种包含阴离子多糖的百草枯组合物及其应用 |
| CN113940352A (zh) * | 2020-07-17 | 2022-01-18 | 汕头市深泰新材料科技发展有限公司 | 一种包含海藻酸盐或其衍生物的减毒百草枯组合物及其应用 |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2263067A (en) * | 1937-12-13 | 1941-11-18 | Borg Warner | Heat transfer |
| US2247622A (en) * | 1939-09-11 | 1941-07-01 | Roy S Thompson | Painting apparatus |
| US4046552A (en) * | 1976-04-15 | 1977-09-06 | Imperial Chemical Industries Limited | Herbicidal compositions of bipyridylium quaternary salts and emetic amounts of s-triazolo pyrimidine derivatives |
| US4400391A (en) * | 1980-01-09 | 1983-08-23 | The United States Of America As Represented By The Secretary Of Agriculture | Controlled release of bioactive materials using alginate gel beads |
| CN1010654B (zh) * | 1984-08-10 | 1990-12-05 | 麦克公司 | 联吡啶季盐固态除草剂组合物的制备方法 |
| US4764206A (en) * | 1985-10-10 | 1988-08-16 | S D S Bioteck K.K. | Contradeglutitious solid herbicidal composition |
| FR2588723B1 (fr) * | 1985-11-12 | 1990-04-13 | Sds Biotech Kk | Composition herbicide solide anti-deglutition contenant du paraquat et un agent epaississant |
| ZA879051B (en) * | 1986-12-03 | 1988-07-27 | Harvest Chemicals Proprietary | A composition for application to a soil or plant locus |
| GB9015134D0 (en) * | 1990-07-10 | 1990-08-29 | Ici Plc | Herbicidal compositions |
| GB2247622A (en) * | 1990-09-05 | 1992-03-11 | Ici Plc | Herbicides |
| GB9200265D0 (en) * | 1992-01-08 | 1992-02-26 | Ici Plc | Herbicidal composition |
| WO1995031903A1 (fr) * | 1994-05-20 | 1995-11-30 | Kao Corporation | Composition herbicide |
| GB9415290D0 (en) * | 1994-07-28 | 1994-09-21 | Zeneca Ltd | Gel formation |
| AU1385197A (en) * | 1996-01-30 | 1997-08-22 | Zeneca Limited | Packaged agrochemical composition |
| MY129957A (en) * | 1996-03-06 | 2007-05-31 | Kao Corp | Aqueous liquid agricultural composition |
| PL195031B1 (pl) * | 1997-04-30 | 2007-08-31 | Reckitt Benckiser Healthcare | Ciekła wodna kompozycja nadająca się do nalewaniazawierająca alginian i wodorowęglan metalu alkalicznego |
| US7008904B2 (en) * | 2000-09-13 | 2006-03-07 | Monsanto Technology, Llc | Herbicidal compositions containing glyphosate and bipyridilium |
-
2001
- 2001-03-27 GB GBGB0107651.2A patent/GB0107651D0/en not_active Ceased
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2002
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- 2002-03-13 EA EA200301060A patent/EA006169B1/ru not_active IP Right Cessation
- 2002-03-13 US US10/472,853 patent/US20040157742A1/en not_active Abandoned
- 2002-03-13 PL PL02363836A patent/PL363836A1/xx not_active Application Discontinuation
- 2002-03-13 AU AU2002242833A patent/AU2002242833B2/en not_active Ceased
- 2002-03-13 YU YU74603A patent/YU74603A/sh unknown
- 2002-03-13 MX MXPA03008621A patent/MXPA03008621A/es active IP Right Grant
- 2002-03-13 EP EP02708470A patent/EP1383384A1/en not_active Withdrawn
- 2002-03-13 AP APAP/P/2003/002869A patent/AP1790A/en active
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- 2002-03-13 CN CNB028073401A patent/CN1288975C/zh not_active Expired - Fee Related
- 2002-03-13 WO PCT/GB2002/001147 patent/WO2002076212A1/en active IP Right Grant
- 2002-03-13 UA UA2003109606A patent/UA76455C2/uk unknown
- 2002-03-13 BR BR0208234-9A patent/BR0208234A/pt not_active IP Right Cessation
- 2002-03-13 SK SK1190-2003A patent/SK11902003A3/sk not_active Application Discontinuation
- 2002-03-13 JP JP2002574740A patent/JP2004524341A/ja active Pending
- 2002-03-13 HU HUP0401309 patent/HUP0401309A2/hu unknown
- 2002-03-14 MY MYPI20020942A patent/MY136351A/en unknown
- 2002-03-19 AR ARP020100988A patent/AR033182A1/es not_active Application Discontinuation
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- 2002-03-25 TW TW091105740A patent/TWI285531B/zh not_active IP Right Cessation
- 2002-03-26 UY UY27229A patent/UY27229A1/es unknown
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- 2002-03-26 KR KR1020020016279A patent/KR100552377B1/ko not_active IP Right Cessation
- 2002-03-27 PE PE2002000247A patent/PE20020942A1/es not_active Application Discontinuation
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2003
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