OA12463A - Composition containing paraquat and/or diquat an alginate and an emetic and/or purgative. - Google Patents

Composition containing paraquat and/or diquat an alginate and an emetic and/or purgative. Download PDF

Info

Publication number: OA12463A
Authority: OA; OAPI
Prior art keywords: composition according; alginate; composition; daims; sait
Prior art date: 2001-03-27

Application number

OA1200300250A

Other languages

English (en)

Inventor

Emma Jane Ashford

Jonathan Roy Heylings

Richa Shaunak

Original Assignee

Syngenta Ltd

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.)

2001-03-27

Filing date

2002-03-13

Publication date

2006-05-24

2002-03-13 Application filed by Syngenta Ltd filed Critical Syngenta Ltd

2006-05-24 Publication of OA12463A publication Critical patent/OA12463A/en

Links

239000000203 mixture Substances 0.000 title claims abstract description 184
229920000615 alginic acid Polymers 0.000 title claims abstract description 48
235000010443 alginic acid Nutrition 0.000 title claims abstract description 48
239000002895 emetic Substances 0.000 title claims abstract description 43
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 title claims abstract description 39
229940072056 alginate Drugs 0.000 title claims abstract description 39
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 title claims abstract description 33
230000001543 purgative effect Effects 0.000 title claims abstract description 20
239000005630 Diquat Substances 0.000 title claims abstract description 18
239000008141 laxative Substances 0.000 title claims abstract description 18
SYJFEGQWDCRVNX-UHFFFAOYSA-N diquat Chemical compound C1=CC=[N+]2CC[N+]3=CC=CC=C3C2=C1 SYJFEGQWDCRVNX-UHFFFAOYSA-N 0.000 title claims abstract description 17
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 27
239000003349 gelling agent Substances 0.000 claims abstract description 21
230000000694 effects Effects 0.000 claims abstract description 16
210000004051 gastric juice Anatomy 0.000 claims abstract description 13
230000001960 triggered effect Effects 0.000 claims abstract description 13
239000002253 acid Substances 0.000 claims abstract description 9
238000004519 manufacturing process Methods 0.000 claims abstract description 3
FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 claims description 26
230000002363 herbicidal effect Effects 0.000 claims description 22
QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 claims description 20
-1 alkyl ethoxy carboxylates Chemical class 0.000 claims description 19
229910021653 sulphate ion Inorganic materials 0.000 claims description 19
239000000243 solution Substances 0.000 claims description 11
239000007787 solid Substances 0.000 claims description 9
150000003973 alkyl amines Chemical class 0.000 claims description 8
150000004996 alkyl benzenes Chemical class 0.000 claims description 7
238000000034 method Methods 0.000 claims description 7
239000011734 sodium Substances 0.000 claims description 7
229910052708 sodium Inorganic materials 0.000 claims description 7
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 5
239000002736 nonionic surfactant Substances 0.000 claims description 5
QXNVGIXVLWOKEQ-UHFFFAOYSA-N Disodium Chemical compound [Na][Na] QXNVGIXVLWOKEQ-UHFFFAOYSA-N 0.000 claims description 4
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 4
239000007864 aqueous solution Substances 0.000 claims description 4
125000002091 cationic group Chemical group 0.000 claims description 4
229920000642 polymer Polymers 0.000 claims description 4
239000004372 Polyvinyl alcohol Substances 0.000 claims description 3
150000001298 alcohols Chemical class 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
229920002451 polyvinyl alcohol Polymers 0.000 claims description 3
235000019422 polyvinyl alcohol Nutrition 0.000 claims description 3
229920005682 EO-PO block copolymer Polymers 0.000 claims description 2
239000002202 Polyethylene glycol Substances 0.000 claims description 2
150000001412 amines Chemical class 0.000 claims description 2
229940077388 benzenesulfonate Drugs 0.000 claims description 2
150000004985 diamines Chemical class 0.000 claims description 2
125000001400 nonyl 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])C([H])([H])[H] 0.000 claims description 2
150000003014 phosphoric acid esters Chemical class 0.000 claims description 2
229920001223 polyethylene glycol Polymers 0.000 claims description 2
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 2
SGPGESCZOCHFCL-UHFFFAOYSA-N Tilisolol hydrochloride Chemical compound [Cl-].C1=CC=C2C(=O)N(C)C=C(OCC(O)C[NH2+]C(C)(C)C)C2=C1 SGPGESCZOCHFCL-UHFFFAOYSA-N 0.000 claims 3
241000196324 Embryophyta Species 0.000 claims 2
URXNVXOMQQCBHS-UHFFFAOYSA-N naphthalene;sodium Chemical compound [Na].C1=CC=CC2=CC=CC=C21 URXNVXOMQQCBHS-UHFFFAOYSA-N 0.000 claims 1
150000003839 salts Chemical class 0.000 abstract description 5
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 1
239000000391 magnesium silicate Substances 0.000 abstract 1
229940099273 magnesium trisilicate Drugs 0.000 abstract 1
229910000386 magnesium trisilicate Inorganic materials 0.000 abstract 1
235000019793 magnesium trisilicate Nutrition 0.000 abstract 1
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 39
INFDPOAKFNIJBF-UHFFFAOYSA-N paraquat Chemical compound C1=C[N+](C)=CC=C1C1=CC=[N+](C)C=C1 INFDPOAKFNIJBF-UHFFFAOYSA-N 0.000 description 16
239000003795 chemical substances by application Substances 0.000 description 14
238000009472 formulation Methods 0.000 description 14
239000004094 surface-active agent Substances 0.000 description 10
239000004009 herbicide Substances 0.000 description 9
239000000443 aerosol Substances 0.000 description 8
239000011575 calcium Substances 0.000 description 8
OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 7
238000010521 absorption reaction Methods 0.000 description 7
229910052791 calcium Inorganic materials 0.000 description 7
239000000375 suspending agent Substances 0.000 description 7
206010047700 Vomiting Diseases 0.000 description 6
125000000129 anionic group Chemical group 0.000 description 6
150000001450 anions Chemical class 0.000 description 6
150000001768 cations Chemical class 0.000 description 6
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 5
230000008673 vomiting Effects 0.000 description 5
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 4
JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 4
229910052799 carbon Inorganic materials 0.000 description 4
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
239000002671 adjuvant Substances 0.000 description 3
239000002518 antifoaming agent Substances 0.000 description 3
YRIUSKIDOIARQF-UHFFFAOYSA-N dodecyl benzenesulfonate Chemical compound CCCCCCCCCCCCOS(=O)(=O)C1=CC=CC=C1 YRIUSKIDOIARQF-UHFFFAOYSA-N 0.000 description 3
229940071161 dodecylbenzenesulfonate Drugs 0.000 description 3
239000000975 dye Substances 0.000 description 3
239000007788 liquid Substances 0.000 description 3
229920001983 poloxamer Polymers 0.000 description 3
210000000813 small intestine Anatomy 0.000 description 3
241000894007 species Species 0.000 description 3
210000002784 stomach Anatomy 0.000 description 3
230000008719 thickening Effects 0.000 description 3
239000002562 thickening agent Substances 0.000 description 3
PWTDXSJCVGCUJD-UHFFFAOYSA-N 4-(8-methylnonoxy)-4-oxo-3-sulfobutanoic acid Chemical compound CC(C)CCCCCCCOC(=O)C(S(O)(=O)=O)CC(O)=O PWTDXSJCVGCUJD-UHFFFAOYSA-N 0.000 description 2
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
239000005562 Glyphosate Substances 0.000 description 2
241000283973 Oryctolagus cuniculus Species 0.000 description 2
ULUAUXLGCMPNKK-UHFFFAOYSA-N Sulfobutanedioic acid Chemical class OC(=O)CC(C(O)=O)S(O)(=O)=O ULUAUXLGCMPNKK-UHFFFAOYSA-N 0.000 description 2
230000002411 adverse Effects 0.000 description 2
230000015572 biosynthetic process Effects 0.000 description 2
JEDYYFXHPAIBGR-UHFFFAOYSA-N butafenacil Chemical compound O=C1N(C)C(C(F)(F)F)=CC(=O)N1C1=CC=C(Cl)C(C(=O)OC(C)(C)C(=O)OCC=C)=C1 JEDYYFXHPAIBGR-UHFFFAOYSA-N 0.000 description 2
150000001875 compounds Chemical class 0.000 description 2
239000012141 concentrate Substances 0.000 description 2
MZZBPDKVEFVLFF-UHFFFAOYSA-N cyanazine Chemical compound CCNC1=NC(Cl)=NC(NC(C)(C)C#N)=N1 MZZBPDKVEFVLFF-UHFFFAOYSA-N 0.000 description 2
239000003205 fragrance Substances 0.000 description 2
230000002496 gastric effect Effects 0.000 description 2
230000030136 gastric emptying Effects 0.000 description 2
210000003736 gastrointestinal content Anatomy 0.000 description 2
210000001035 gastrointestinal tract Anatomy 0.000 description 2
238000002156 mixing Methods 0.000 description 2
230000007935 neutral effect Effects 0.000 description 2
230000003204 osmotic effect Effects 0.000 description 2
UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 2
239000007921 spray Substances 0.000 description 2
239000000725 suspension Substances 0.000 description 2
VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 2
NQPDZGIKBAWPEJ-UHFFFAOYSA-N valeric acid Chemical compound CCCCC(O)=O NQPDZGIKBAWPEJ-UHFFFAOYSA-N 0.000 description 2
QIVUCLWGARAQIO-OLIXTKCUSA-N (3s)-n-[(3s,5s,6r)-6-methyl-2-oxo-1-(2,2,2-trifluoroethyl)-5-(2,3,6-trifluorophenyl)piperidin-3-yl]-2-oxospiro[1h-pyrrolo[2,3-b]pyridine-3,6'-5,7-dihydrocyclopenta[b]pyridine]-3'-carboxamide Chemical compound C1([C@H]2[C@H](N(C(=O)[C@@H](NC(=O)C=3C=C4C[C@]5(CC4=NC=3)C3=CC=CN=C3NC5=O)C2)CC(F)(F)F)C)=C(F)C=CC(F)=C1F QIVUCLWGARAQIO-OLIXTKCUSA-N 0.000 description 1
LNGRZPZKVUBWQV-UHFFFAOYSA-N (4-chloro-2-methylsulfonylphenyl)-(5-cyclopropyl-1,2-oxazol-4-yl)methanone Chemical compound CS(=O)(=O)C1=CC(Cl)=CC=C1C(=O)C1=C(C2CC2)ON=C1 LNGRZPZKVUBWQV-UHFFFAOYSA-N 0.000 description 1
WVQBLGZPHOPPFO-LBPRGKRZSA-N (S)-metolachlor Chemical compound CCC1=CC=CC(C)=C1N([C@@H](C)COC)C(=O)CCl WVQBLGZPHOPPFO-LBPRGKRZSA-N 0.000 description 1
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
WTFAGPBUAGFMQX-UHFFFAOYSA-N 1-[2-[2-(2-aminopropoxy)propoxy]propoxy]propan-2-amine Chemical compound CC(N)COCC(C)OCC(C)OCC(C)N WTFAGPBUAGFMQX-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
239000005631 2,4-Dichlorophenoxyacetic acid Substances 0.000 description 1
WJZBEAFISWYEOJ-UHFFFAOYSA-N 2-(2-aminoethoxy)ethyl hydrogen sulfate;2-[bis(2-hydroxyethyl)amino]ethanol Chemical compound OCCN(CCO)CCO.NCCOCCOS(O)(=O)=O WJZBEAFISWYEOJ-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
CLQMBPJKHLGMQK-UHFFFAOYSA-N 2-(4-isopropyl-4-methyl-5-oxo-4,5-dihydro-1H-imidazol-2-yl)nicotinic acid Chemical compound N1C(=O)C(C(C)C)(C)N=C1C1=NC=CC=C1C(O)=O CLQMBPJKHLGMQK-UHFFFAOYSA-N 0.000 description 1
IRJQWZWMQCVOLA-ZBKNUEDVSA-N 2-[(z)-n-[(3,5-difluorophenyl)carbamoylamino]-c-methylcarbonimidoyl]pyridine-3-carboxylic acid Chemical compound N=1C=CC=C(C(O)=O)C=1C(/C)=N\NC(=O)NC1=CC(F)=CC(F)=C1 IRJQWZWMQCVOLA-ZBKNUEDVSA-N 0.000 description 1
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
IAJOBQBIJHVGMQ-UHFFFAOYSA-N 2-amino-4-[hydroxy(methyl)phosphoryl]butanoic acid Chemical compound CP(O)(=O)CCC(N)C(O)=O IAJOBQBIJHVGMQ-UHFFFAOYSA-N 0.000 description 1
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 description 1
LLWADFLAOKUBDR-UHFFFAOYSA-N 2-methyl-4-chlorophenoxybutyric acid Chemical compound CC1=CC(Cl)=CC=C1OCCCC(O)=O LLWADFLAOKUBDR-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
XMTQQYYKAHVGBJ-UHFFFAOYSA-N 3-(3,4-DICHLOROPHENYL)-1,1-DIMETHYLUREA Chemical compound CN(C)C(=O)NC1=CC=C(Cl)C(Cl)=C1 XMTQQYYKAHVGBJ-UHFFFAOYSA-N 0.000 description 1
MBFHUWCOCCICOK-UHFFFAOYSA-N 4-iodo-2-[(4-methoxy-6-methyl-1,3,5-triazin-2-yl)carbamoylsulfamoyl]benzoic acid Chemical compound COC1=NC(C)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=C(I)C=2)C(O)=O)=N1 MBFHUWCOCCICOK-UHFFFAOYSA-N 0.000 description 1
FZLSDZZNPXXBBB-KDURUIRLSA-N 5-chloro-N-[3-cyclopropyl-5-[[(3R,5S)-3,5-dimethylpiperazin-1-yl]methyl]phenyl]-4-(6-methyl-1H-indol-3-yl)pyrimidin-2-amine Chemical compound C[C@H]1CN(Cc2cc(Nc3ncc(Cl)c(n3)-c3c[nH]c4cc(C)ccc34)cc(c2)C2CC2)C[C@@H](C)N1 FZLSDZZNPXXBBB-KDURUIRLSA-N 0.000 description 1
ZUSHSDOEVHPTCU-UHFFFAOYSA-N 6-chloro-3-phenyl-1h-pyridazin-4-one Chemical compound N1C(Cl)=CC(=O)C(C=2C=CC=CC=2)=N1 ZUSHSDOEVHPTCU-UHFFFAOYSA-N 0.000 description 1
GJCOSYZMQJWQCA-UHFFFAOYSA-N 9H-xanthene Chemical compound C1=CC=C2CC3=CC=CC=C3OC2=C1 GJCOSYZMQJWQCA-UHFFFAOYSA-N 0.000 description 1
QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
239000002890 Aclonifen Substances 0.000 description 1
KLSJWNVTNUYHDU-UHFFFAOYSA-N Amitrole Chemical compound NC1=NC=NN1 KLSJWNVTNUYHDU-UHFFFAOYSA-N 0.000 description 1
PFJJMJDEVDLPNE-UHFFFAOYSA-N Benoxacor Chemical compound C1=CC=C2N(C(=O)C(Cl)Cl)C(C)COC2=C1 PFJJMJDEVDLPNE-UHFFFAOYSA-N 0.000 description 1
241001474374 Blennius Species 0.000 description 1
101000742062 Bos taurus Protein phosphatase 1G Proteins 0.000 description 1
CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 1
239000005489 Bromoxynil Substances 0.000 description 1
BMTAFVWTTFSTOG-UHFFFAOYSA-N Butylate Chemical compound CCSC(=O)N(CC(C)C)CC(C)C BMTAFVWTTFSTOG-UHFFFAOYSA-N 0.000 description 1
FERIUCNNQQJTOY-UHFFFAOYSA-M Butyrate Chemical compound CCCC([O-])=O FERIUCNNQQJTOY-UHFFFAOYSA-M 0.000 description 1
FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Natural products CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 description 1
239000005492 Carfentrazone-ethyl Substances 0.000 description 1
VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
KRKNYBCHXYNGOX-UHFFFAOYSA-K Citrate Chemical compound [O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O KRKNYBCHXYNGOX-UHFFFAOYSA-K 0.000 description 1
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239000005500 Clopyralid Substances 0.000 description 1
229940126062 Compound A Drugs 0.000 description 1
AEMOLEFTQBMNLQ-VANFPWTGSA-N D-mannopyranuronic acid Chemical compound OC1O[C@H](C(O)=O)[C@@H](O)[C@H](O)[C@@H]1O AEMOLEFTQBMNLQ-VANFPWTGSA-N 0.000 description 1
239000005504 Dicamba Substances 0.000 description 1
YRMLFORXOOIJDR-UHFFFAOYSA-N Dichlormid Chemical compound ClC(Cl)C(=O)N(CC=C)CC=C YRMLFORXOOIJDR-UHFFFAOYSA-N 0.000 description 1
QNXAVFXEJCPCJO-UHFFFAOYSA-N Diclosulam Chemical compound N=1N2C(OCC)=NC(F)=CC2=NC=1S(=O)(=O)NC1=C(Cl)C=CC=C1Cl QNXAVFXEJCPCJO-UHFFFAOYSA-N 0.000 description 1
239000005510 Diuron Substances 0.000 description 1
NRFQZTCQAYEXEE-UHFFFAOYSA-N Fenclorim Chemical compound ClC1=CC(Cl)=NC(C=2C=CC=CC=2)=N1 NRFQZTCQAYEXEE-UHFFFAOYSA-N 0.000 description 1
239000005529 Florasulam Substances 0.000 description 1
QZXATCCPQKOEIH-UHFFFAOYSA-N Florasulam Chemical compound N=1N2C(OC)=NC=C(F)C2=NC=1S(=O)(=O)NC1=C(F)C=CC=C1F QZXATCCPQKOEIH-UHFFFAOYSA-N 0.000 description 1
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IRECWLYBCAZIJM-UHFFFAOYSA-N Flumiclorac pentyl Chemical group C1=C(Cl)C(OCC(=O)OCCCCC)=CC(N2C(C3=C(CCCC3)C2=O)=O)=C1F IRECWLYBCAZIJM-UHFFFAOYSA-N 0.000 description 1
239000005558 Fluroxypyr Substances 0.000 description 1
UKSLKNUCVPZQCQ-UHFFFAOYSA-N Fluxofenim Chemical compound C=1C=C(Cl)C=CC=1C(C(F)(F)F)=NOCC1OCCO1 UKSLKNUCVPZQCQ-UHFFFAOYSA-N 0.000 description 1
239000005560 Foramsulfuron Substances 0.000 description 1
IAJILQKETJEXLJ-UHFFFAOYSA-N Galacturonsaeure Natural products O=CC(O)C(O)C(O)C(O)C(O)=O IAJILQKETJEXLJ-UHFFFAOYSA-N 0.000 description 1
239000005561 Glufosinate Substances 0.000 description 1
239000005564 Halosulfuron methyl Substances 0.000 description 1
FMGZEUWROYGLAY-UHFFFAOYSA-N Halosulfuron-methyl Chemical group ClC1=NN(C)C(S(=O)(=O)NC(=O)NC=2N=C(OC)C=C(OC)N=2)=C1C(=O)OC FMGZEUWROYGLAY-UHFFFAOYSA-N 0.000 description 1
NLDMNSXOCDLTTB-UHFFFAOYSA-N Heterophylliin A Natural products O1C2COC(=O)C3=CC(O)=C(O)C(O)=C3C3=C(O)C(O)=C(O)C=C3C(=O)OC2C(OC(=O)C=2C=C(O)C(O)=C(O)C=2)C(O)C1OC(=O)C1=CC(O)=C(O)C(O)=C1 NLDMNSXOCDLTTB-UHFFFAOYSA-N 0.000 description 1
239000005566 Imazamox Substances 0.000 description 1
239000005981 Imazaquin Substances 0.000 description 1
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239000005571 Isoxaflutole Substances 0.000 description 1
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239000005575 MCPB Substances 0.000 description 1
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239000005578 Mesotrione Substances 0.000 description 1
239000005582 Metosulam Substances 0.000 description 1
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239000005583 Metribuzin Substances 0.000 description 1
229910002651 NO3 Inorganic materials 0.000 description 1
239000005586 Nicosulfuron Substances 0.000 description 1
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206010058667 Oral toxicity Diseases 0.000 description 1
229910019142 PO4 Inorganic materials 0.000 description 1
239000005591 Pendimethalin Substances 0.000 description 1
GPGLBXMQFQQXDV-UHFFFAOYSA-N Primisulfuron Chemical compound OC(=O)C1=CC=CC=C1S(=O)(=O)NC(=O)NC1=NC(OC(F)F)=CC(OC(F)F)=N1 GPGLBXMQFQQXDV-UHFFFAOYSA-N 0.000 description 1
XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 description 1
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239000005604 Prosulfuron Substances 0.000 description 1
LTUNNEGNEKBSEH-UHFFFAOYSA-N Prosulfuron Chemical compound COC1=NC(C)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2)CCC(F)(F)F)=N1 LTUNNEGNEKBSEH-UHFFFAOYSA-N 0.000 description 1
239000005606 Pyridate Substances 0.000 description 1
JTZCTMAVMHRNTR-UHFFFAOYSA-N Pyridate Chemical compound CCCCCCCCSC(=O)OC1=CC(Cl)=NN=C1C1=CC=CC=C1 JTZCTMAVMHRNTR-UHFFFAOYSA-N 0.000 description 1
239000005616 Rimsulfuron Substances 0.000 description 1
239000005617 S-Metolachlor Substances 0.000 description 1
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 1
DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 description 1
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DDBMQDADIHOWIC-UHFFFAOYSA-N aclonifen Chemical compound C1=C([N+]([O-])=O)C(N)=C(Cl)C(OC=2C=CC=CC=2)=C1 DDBMQDADIHOWIC-UHFFFAOYSA-N 0.000 description 1
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XCSGPAVHZFQHGE-UHFFFAOYSA-N alachlor Chemical compound CCC1=CC=CC(CC)=C1N(COC)C(=O)CCl XCSGPAVHZFQHGE-UHFFFAOYSA-N 0.000 description 1
125000000217 alkyl group Chemical group 0.000 description 1
RQVYBGPQFYCBGX-UHFFFAOYSA-N ametryn Chemical compound CCNC1=NC(NC(C)C)=NC(SC)=N1 RQVYBGPQFYCBGX-UHFFFAOYSA-N 0.000 description 1
ORFPWVRKFLOQHK-UHFFFAOYSA-N amicarbazone Chemical compound CC(C)C1=NN(C(=O)NC(C)(C)C)C(=O)N1N ORFPWVRKFLOQHK-UHFFFAOYSA-N 0.000 description 1
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229920006318 anionic polymer Polymers 0.000 description 1
239000013011 aqueous formulation Substances 0.000 description 1
239000008346 aqueous phase Substances 0.000 description 1
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XOEMATDHVZOBSG-UHFFFAOYSA-N azafenidin Chemical compound C1=C(OCC#C)C(Cl)=CC(Cl)=C1N1C(=O)N2CCCCC2=N1 XOEMATDHVZOBSG-UHFFFAOYSA-N 0.000 description 1
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SRSXLGNVWSONIS-UHFFFAOYSA-M benzenesulfonate Chemical compound [O-]S(=O)(=O)C1=CC=CC=C1 SRSXLGNVWSONIS-UHFFFAOYSA-M 0.000 description 1
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AEMOLEFTQBMNLQ-UHFFFAOYSA-N beta-D-galactopyranuronic acid Natural products OC1OC(C(O)=O)C(O)C(O)C1O AEMOLEFTQBMNLQ-UHFFFAOYSA-N 0.000 description 1
229920001400 block copolymer Polymers 0.000 description 1
239000008280 blood Substances 0.000 description 1
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MXZACTZQSGYANA-UHFFFAOYSA-N chembl545463 Chemical compound Cl.C1=CC(OC)=CC=C1C(N=C1)=CN2C1=NC(C)=C2O MXZACTZQSGYANA-UHFFFAOYSA-N 0.000 description 1
KIEDNEWSYUYDSN-UHFFFAOYSA-N clomazone Chemical compound O=C1C(C)(C)CON1CC1=CC=CC=C1Cl KIEDNEWSYUYDSN-UHFFFAOYSA-N 0.000 description 1
HUBANNPOLNYSAD-UHFFFAOYSA-N clopyralid Chemical compound OC(=O)C1=NC(Cl)=CC=C1Cl HUBANNPOLNYSAD-UHFFFAOYSA-N 0.000 description 1
YIANBKOBVRMNPR-UHFFFAOYSA-N cloransulam Chemical compound N=1N2C(OCC)=NC(F)=CC2=NC=1S(=O)(=O)NC1=C(Cl)C=CC=C1C(O)=O YIANBKOBVRMNPR-UHFFFAOYSA-N 0.000 description 1
239000000084 colloidal system Substances 0.000 description 1
AEMOLEFTQBMNLQ-YBSDWZGDSA-N d-mannuronic acid Chemical compound O[C@@H]1O[C@@H](C(O)=O)[C@H](O)[C@@H](O)[C@H]1O AEMOLEFTQBMNLQ-YBSDWZGDSA-N 0.000 description 1
IWEDIXLBFLAXBO-UHFFFAOYSA-N dicamba Chemical compound COC1=C(Cl)C=CC(Cl)=C1C(O)=O IWEDIXLBFLAXBO-UHFFFAOYSA-N 0.000 description 1
235000014113 dietary fatty acids Nutrition 0.000 description 1
239000012895 dilution Substances 0.000 description 1
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235000019329 dioctyl sodium sulphosuccinate Nutrition 0.000 description 1
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KHIQYZGEUSTKSB-UHFFFAOYSA-L disodium;4-dodecoxy-4-oxo-3-sulfobutanoate Chemical compound [Na+].[Na+].CCCCCCCCCCCCOC(=O)C(S(O)(=O)=O)CC([O-])=O.CCCCCCCCCCCCOC(=O)C(S(O)(=O)=O)CC([O-])=O KHIQYZGEUSTKSB-UHFFFAOYSA-L 0.000 description 1
239000012153 distilled water Substances 0.000 description 1
GVGUFUZHNYFZLC-UHFFFAOYSA-N dodecyl benzenesulfonate;sodium Chemical compound [Na].CCCCCCCCCCCCOS(=O)(=O)C1=CC=CC=C1 GVGUFUZHNYFZLC-UHFFFAOYSA-N 0.000 description 1
150000002148 esters Chemical class 0.000 description 1
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238000002474 experimental method Methods 0.000 description 1
229930195729 fatty acid Natural products 0.000 description 1
239000000194 fatty acid Substances 0.000 description 1
150000004665 fatty acids Chemical class 0.000 description 1
IANUJLZYFUDJIH-UHFFFAOYSA-N flufenacet Chemical compound C=1C=C(F)C=CC=1N(C(C)C)C(=O)COC1=NN=C(C(F)(F)F)S1 IANUJLZYFUDJIH-UHFFFAOYSA-N 0.000 description 1
FOUWCSDKDDHKQP-UHFFFAOYSA-N flumioxazin Chemical compound FC1=CC=2OCC(=O)N(CC#C)C=2C=C1N(C1=O)C(=O)C2=C1CCCC2 FOUWCSDKDDHKQP-UHFFFAOYSA-N 0.000 description 1
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MEFQWPUMEMWTJP-UHFFFAOYSA-N fluroxypyr Chemical compound NC1=C(Cl)C(F)=NC(OCC(O)=O)=C1Cl MEFQWPUMEMWTJP-UHFFFAOYSA-N 0.000 description 1
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
239000006260 foam Substances 0.000 description 1
235000013305 food Nutrition 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
CSRCNKZJIYKJOT-UHFFFAOYSA-N formaldehyde;naphthalene;sodium Chemical compound [Na].O=C.C1=CC=CC2=CC=CC=C21 CSRCNKZJIYKJOT-UHFFFAOYSA-N 0.000 description 1
VZCYOOQTPOCHFL-OWOJBTEDSA-L fumarate(2-) Chemical compound [O-]C(=O)\C=C\C([O-])=O VZCYOOQTPOCHFL-OWOJBTEDSA-L 0.000 description 1
IAJOBQBIJHVGMQ-BYPYZUCNSA-N glufosinate-P Chemical compound CP(O)(=O)CC[C@H](N)C(O)=O IAJOBQBIJHVGMQ-BYPYZUCNSA-N 0.000 description 1
150000004676 glycans Chemical class 0.000 description 1
229940097068 glyphosate Drugs 0.000 description 1
XDDAORKBJWWYJS-UHFFFAOYSA-M glyphosate(1-) Chemical compound OP(O)(=O)CNCC([O-])=O XDDAORKBJWWYJS-UHFFFAOYSA-M 0.000 description 1
125000005613 guluronic acid group Chemical group 0.000 description 1
230000009931 harmful effect Effects 0.000 description 1
XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 1
ZMZDMBWJUHKJPS-UHFFFAOYSA-N hydrogen thiocyanate Natural products SC#N ZMZDMBWJUHKJPS-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
150000008040 ionic compounds Chemical class 0.000 description 1
OYIKARCXOQLFHF-UHFFFAOYSA-N isoxaflutole Chemical compound CS(=O)(=O)C1=CC(C(F)(F)F)=CC=C1C(=O)C1=C(C2CC2)ON=C1 OYIKARCXOQLFHF-UHFFFAOYSA-N 0.000 description 1
229940088649 isoxaflutole Drugs 0.000 description 1
239000011344 liquid material Substances 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
239000000463 material Substances 0.000 description 1
KPUREKXXPHOJQT-UHFFFAOYSA-N mesotrione Chemical compound [O-][N+](=O)C1=CC(S(=O)(=O)C)=CC=C1C(=O)C1C(=O)CCCC1=O KPUREKXXPHOJQT-UHFFFAOYSA-N 0.000 description 1
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
210000004877 mucosa Anatomy 0.000 description 1
VOVZXURTCKPRDQ-CQSZACIVSA-N n-[4-[chloro(difluoro)methoxy]phenyl]-6-[(3r)-3-hydroxypyrrolidin-1-yl]-5-(1h-pyrazol-5-yl)pyridine-3-carboxamide Chemical compound C1[C@H](O)CCN1C1=NC=C(C(=O)NC=2C=CC(OC(F)(F)Cl)=CC=2)C=C1C1=CC=NN1 VOVZXURTCKPRDQ-CQSZACIVSA-N 0.000 description 1
CHEDHKBPPDKBQF-UPONEAKYSA-N n-[5-[(6s,7ar)-6-fluoro-1,3-dioxo-5,6,7,7a-tetrahydropyrrolo[1,2-c]imidazol-2-yl]-2-chloro-4-fluorophenyl]-1-chloromethanesulfonamide Chemical compound N1([C@@H](C2=O)C[C@@H](C1)F)C(=O)N2C1=CC(NS(=O)(=O)CCl)=C(Cl)C=C1F CHEDHKBPPDKBQF-UPONEAKYSA-N 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
229910021414 novamene Inorganic materials 0.000 description 1
231100000418 oral toxicity Toxicity 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
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
239000010452 phosphate Substances 0.000 description 1
239000000049 pigment Substances 0.000 description 1
229920001282 polysaccharide Polymers 0.000 description 1
239000005017 polysaccharide Substances 0.000 description 1
AAEVYOVXGOFMJO-UHFFFAOYSA-N prometryn Chemical compound CSC1=NC(NC(C)C)=NC(NC(C)C)=N1 AAEVYOVXGOFMJO-UHFFFAOYSA-N 0.000 description 1
FKLQIONHGSFYJY-UHFFFAOYSA-N propan-2-yl 5-[4-bromo-1-methyl-5-(trifluoromethyl)pyrazol-3-yl]-2-chloro-4-fluorobenzoate Chemical compound C1=C(Cl)C(C(=O)OC(C)C)=CC(C=2C(=C(N(C)N=2)C(F)(F)F)Br)=C1F FKLQIONHGSFYJY-UHFFFAOYSA-N 0.000 description 1
108090000623 proteins and genes Proteins 0.000 description 1
102000004169 proteins and genes Human genes 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
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
APSBXTVYXVQYAB-UHFFFAOYSA-M sodium docusate Chemical compound [Na+].CCCCC(CC)COC(=O)CC(S([O-])(=O)=O)C(=O)OCC(CC)CCCC APSBXTVYXVQYAB-UHFFFAOYSA-M 0.000 description 1
229940080264 sodium dodecylbenzenesulfonate Drugs 0.000 description 1
SLBXZQMMERXQAL-UHFFFAOYSA-M sodium;1-dodecoxy-4-hydroxy-1,4-dioxobutane-2-sulfonate Chemical compound [Na+].CCCCCCCCCCCCOC(=O)C(S(O)(=O)=O)CC([O-])=O SLBXZQMMERXQAL-UHFFFAOYSA-M 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
230000002195 synergetic effect Effects 0.000 description 1
230000009885 systemic 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
229920001285 xanthan gum Polymers 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)

OA1200300250A 2001-03-27 2002-03-13 Composition containing paraquat and/or diquat an alginate and an emetic and/or purgative. OA12463A (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
GBGB0107651.2A GB0107651D0 (en)	2001-03-27	2001-03-27	Composition

Publications (1)

Publication Number	Publication Date
OA12463A true OA12463A (en)	2006-05-24

Family

ID=9911668

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
OA1200300250A OA12463A (en)	2001-03-27	2002-03-13	Composition containing paraquat and/or diquat an alginate and an emetic and/or purgative.

Country Status (39)

Country	Link
US (1)	US20040157742A1 (fr)
EP (1)	EP1383384A1 (fr)
JP (1)	JP2004524341A (fr)
KR (1)	KR100552377B1 (fr)
CN (1)	CN1288975C (fr)
AP (1)	AP1790A (fr)
AR (1)	AR033182A1 (fr)
AU (1)	AU2002242833B2 (fr)
BG (1)	BG108194A (fr)
BR (1)	BR0208234A (fr)
CA (1)	CA2440360A1 (fr)
CZ (1)	CZ20032577A3 (fr)
DO (1)	DOP2002000369A (fr)
EA (1)	EA006169B1 (fr)
EC (1)	ECSP034777A (fr)
EE (1)	EE200300461A (fr)
EG (1)	EG23378A (fr)
GB (1)	GB0107651D0 (fr)
GE (1)	GEP20063980B (fr)
HR (1)	HRP20030779A2 (fr)
HU (1)	HUP0401309A2 (fr)
IL (1)	IL158055A0 (fr)
MA (1)	MA26013A1 (fr)
MX (1)	MXPA03008621A (fr)
MY (1)	MY136351A (fr)
NO (1)	NO20034304L (fr)
NZ (1)	NZ528116A (fr)
OA (1)	OA12463A (fr)
PA (1)	PA8542501A1 (fr)
PE (1)	PE20020942A1 (fr)
PL (1)	PL363836A1 (fr)
SK (1)	SK11902003A3 (fr)
TN (1)	TNSN03081A1 (fr)
TW (1)	TWI285531B (fr)
UA (1)	UA76455C2 (fr)
UY (1)	UY27229A1 (fr)
WO (1)	WO2002076212A1 (fr)
YU (1)	YU74603A (fr)
ZA (1)	ZA200307170B (fr)

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GB0301279D0 (en) *	2003-01-20	2003-02-19	Syngenta Ltd	Method of dermal protection
GB0328529D0 (en) *	2003-12-09	2004-01-14	Syngenta Ltd	Agrochemical composition
US20070082819A1 (en) *	2003-12-09	2007-04-12	Perry Richard B	Agrochemical compositions
GB0328528D0 (en) *	2003-12-09	2004-01-14	Syngenta Ltd	Agrochemical composition
WO2006118562A1 (fr) *	2005-04-29	2006-11-09	Inkine Pharmaceutical Company, Inc.	Composition purgative et utilisations
KR100699672B1 (ko) *	2005-10-28	2007-03-23	시논 코포레이션	제초제 조성물
PT2273878T (pt) *	2008-04-08	2017-03-03	Bayer Cropscience Lp	Composição e sistema para a manutenção de relva
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
BR112019028193A2 (pt) *	2017-07-06	2020-07-07	Rhodia Operations	composições pesticidas
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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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
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GB2247622A (en) *	1990-09-05	1992-03-11	Ici Plc	Herbicides
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GB9415290D0 (en) *	1994-07-28	1994-09-21	Zeneca Ltd	Gel formation
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MY129957A (en) *	1996-03-06	2007-05-31	Kao Corp	Aqueous liquid agricultural composition
EP0979091A1 (fr) *	1997-04-30	2000-02-16	Reckitt Benckiser Healthcare (UK) Limited	Compositions d'alginate pouvant etre versees
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2001
- 2001-03-27 GB GBGB0107651.2A patent/GB0107651D0/en not_active Ceased
2002
- 2002-03-13 EE EEP200300461A patent/EE200300461A/xx unknown
- 2002-03-13 CZ CZ20032577A patent/CZ20032577A3/cs unknown
- 2002-03-13 JP JP2002574740A patent/JP2004524341A/ja active Pending
- 2002-03-13 EP EP02708470A patent/EP1383384A1/fr not_active Withdrawn
- 2002-03-13 GE GE5331A patent/GEP20063980B/en unknown
- 2002-03-13 SK SK1190-2003A patent/SK11902003A3/sk not_active Application Discontinuation
- 2002-03-13 CA CA002440360A patent/CA2440360A1/fr not_active Abandoned
- 2002-03-13 AU AU2002242833A patent/AU2002242833B2/en not_active Ceased
- 2002-03-13 HR HR20030779A patent/HRP20030779A2/xx not_active Application Discontinuation
- 2002-03-13 YU YU74603A patent/YU74603A/sh unknown
- 2002-03-13 IL IL15805502A patent/IL158055A0/xx not_active IP Right Cessation
- 2002-03-13 CN CNB028073401A patent/CN1288975C/zh not_active Expired - Fee Related
- 2002-03-13 UA UA2003109606A patent/UA76455C2/uk unknown
- 2002-03-13 AP APAP/P/2003/002869A patent/AP1790A/en active
- 2002-03-13 WO PCT/GB2002/001147 patent/WO2002076212A1/fr not_active Ceased
- 2002-03-13 MX MXPA03008621A patent/MXPA03008621A/es active IP Right Grant
- 2002-03-13 BR BR0208234-9A patent/BR0208234A/pt not_active IP Right Cessation
- 2002-03-13 NZ NZ528116A patent/NZ528116A/en unknown
- 2002-03-13 OA OA1200300250A patent/OA12463A/en unknown
- 2002-03-13 US US10/472,853 patent/US20040157742A1/en not_active Abandoned
- 2002-03-13 HU HUP0401309 patent/HUP0401309A2/hu unknown
- 2002-03-13 EA EA200301060A patent/EA006169B1/ru not_active IP Right Cessation
- 2002-03-13 PL PL02363836A patent/PL363836A1/xx not_active Application Discontinuation
- 2002-03-14 MY MYPI20020942A patent/MY136351A/en unknown
- 2002-03-19 AR ARP020100988A patent/AR033182A1/es not_active Application Discontinuation
- 2002-03-25 DO DO2002000369A patent/DOP2002000369A/es unknown
- 2002-03-25 TW TW091105740A patent/TWI285531B/zh not_active IP Right Cessation
- 2002-03-26 UY UY27229A patent/UY27229A1/es unknown
- 2002-03-26 EG EG20020312A patent/EG23378A/xx active
- 2002-03-26 KR KR1020020016279A patent/KR100552377B1/ko not_active Expired - Fee Related
- 2002-03-27 PA PA20028542501A patent/PA8542501A1/es unknown
- 2002-03-27 PE PE2002000247A patent/PE20020942A1/es not_active Application Discontinuation
2003
- 2003-07-08 TN TNPCT/GB2002/001147A patent/TNSN03081A1/en unknown
- 2003-09-12 ZA ZA200307170A patent/ZA200307170B/en unknown
- 2003-09-24 BG BG108194A patent/BG108194A/bg unknown
- 2003-09-24 EC EC2003004777A patent/ECSP034777A/es unknown
- 2003-09-26 NO NO20034304A patent/NO20034304L/no not_active Application Discontinuation
- 2003-10-10 MA MA27351A patent/MA26013A1/fr unknown

Also Published As

Publication number	Publication date
CN1288975C (zh)	2006-12-13
MXPA03008621A (es)	2005-03-07
UY27229A1 (es)	2002-07-31
MA26013A1 (fr)	2003-12-31
US20040157742A1 (en)	2004-08-12
AP2003002869A0 (en)	2003-09-30
ECSP034777A (es)	2003-10-28
BR0208234A (pt)	2004-03-09
EA006169B1 (ru)	2005-10-27
GB0107651D0 (en)	2001-05-16
DOP2002000369A (es)	2003-01-15
KR100552377B1 (ko)	2006-02-16
HRP20030779A2 (en)	2005-08-31
EE200300461A (et)	2003-12-15
NO20034304D0 (no)	2003-09-26
CZ20032577A3 (cs)	2003-12-17
AU2002242833B2 (en)	2007-07-05
YU74603A (sh)	2006-08-17
NZ528116A (en)	2004-09-24
BG108194A (bg)	2004-09-30
HUP0401309A2 (en)	2004-12-28
PE20020942A1 (es)	2002-12-27
WO2002076212A1 (fr)	2002-10-03
GEP20063980B (en)	2006-12-11
EG23378A (en)	2005-02-28
TWI285531B (en)	2007-08-21
EP1383384A1 (fr)	2004-01-28
PA8542501A1 (es)	2002-10-28
PL363836A1 (en)	2004-11-29
ZA200307170B (en)	2004-07-07
NO20034304L (no)	2003-11-26
KR20020076158A (ko)	2002-10-09
AR033182A1 (es)	2003-12-10
IL158055A0 (en)	2004-03-28
CN1499931A (zh)	2004-05-26
SK11902003A3 (sk)	2004-03-02
EA200301060A1 (ru)	2004-02-26
MY136351A (en)	2008-09-30
AP1790A (en)	2007-10-06
UA76455C2 (en)	2006-08-15
JP2004524341A (ja)	2004-08-12
TNSN03081A1 (en)	2005-04-08
CA2440360A1 (fr)	2002-10-03

Publication	Publication Date	Title
OA12463A (en)	2006-05-24	Composition containing paraquat and/or diquat an alginate and an emetic and/or purgative.
US5017369A (en)	1991-05-21	Film-forming teat sealer for prevention of mastitis and use thereof
AU2002242833A1 (en)	2003-03-27	Composition containing paraquat and/or diquat an alginate and an emetic and/or purgative
CA2415159C (fr)	2011-06-21	Composition antimicrobienne utile dans le traitement de la mastite bovine
JP5065244B2 (ja)	2012-10-31	オレフィン安定剤を有する酸性化された亜塩素酸塩殺菌組成物
CA1297693C (fr)	1992-03-24	Mode de production d'emulsions
JP2008537954A5 (fr)	2009-06-18
FI102939B (fi)	1999-03-31	Herbisidisiä koostumuksia
OA12979A (en)	2006-10-13	Method of dermal protection.
JPS62201803A (ja)	1987-09-05	除草剤組成物
JPS6135964B2 (fr)	1986-08-15
GB1577317A (en)	1980-10-22	Herbicidal compositions
HK1088542A (en)	2006-11-10	Method of dermal protection
CN115581236A (zh)	2023-01-10	二溴海因消毒母液，及其原料组合物、制备方法和应用