UA72760C2 - Method to treat plant foliage - Google Patents
Method to treat plant foliage Download PDFInfo
- Publication number
- UA72760C2 UA72760C2 UA2001117999A UA2001117999A UA72760C2 UA 72760 C2 UA72760 C2 UA 72760C2 UA 2001117999 A UA2001117999 A UA 2001117999A UA 2001117999 A UA2001117999 A UA 2001117999A UA 72760 C2 UA72760 C2 UA 72760C2
- Authority
- UA
- Ukraine
- Prior art keywords
- glyphosate
- composition
- compositions
- amine
- polyoxyethylene
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims abstract description 94
- 239000000203 mixture Substances 0.000 claims abstract description 510
- 239000004094 surface-active agent Substances 0.000 claims abstract description 268
- 239000005562 Glyphosate Substances 0.000 claims abstract description 240
- XDDAORKBJWWYJS-UHFFFAOYSA-N glyphosate Chemical compound OC(=O)CNCP(O)(O)=O XDDAORKBJWWYJS-UHFFFAOYSA-N 0.000 claims abstract description 240
- 229940097068 glyphosate Drugs 0.000 claims abstract description 240
- 239000000126 substance Substances 0.000 claims abstract description 154
- 238000011282 treatment Methods 0.000 claims abstract description 145
- 150000001412 amines Chemical class 0.000 claims abstract description 114
- 230000002363 herbicidal effect Effects 0.000 claims abstract description 112
- 125000000129 anionic group Chemical group 0.000 claims abstract description 91
- 150000005215 alkyl ethers Chemical class 0.000 claims abstract description 74
- 239000004009 herbicide Substances 0.000 claims abstract description 72
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 48
- 239000001257 hydrogen Substances 0.000 claims abstract description 34
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 34
- 239000002253 acid Substances 0.000 claims abstract description 23
- 150000002431 hydrogen Chemical group 0.000 claims abstract description 19
- 230000004071 biological effect Effects 0.000 claims abstract description 15
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 15
- 125000001183 hydrocarbyl group Chemical group 0.000 claims abstract description 14
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims abstract description 14
- 229920006395 saturated elastomer Polymers 0.000 claims abstract description 11
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims abstract description 10
- 125000001931 aliphatic group Chemical group 0.000 claims abstract description 6
- 230000002262 irrigation Effects 0.000 claims abstract description 5
- 238000003973 irrigation Methods 0.000 claims abstract description 5
- 241000196324 Embryophyta Species 0.000 claims description 149
- -1 polyoxyethylene chains Polymers 0.000 claims description 102
- 239000012141 concentrate Substances 0.000 claims description 90
- 125000006353 oxyethylene group Chemical group 0.000 claims description 62
- 229920003171 Poly (ethylene oxide) Polymers 0.000 claims description 57
- 239000013543 active substance Substances 0.000 claims description 52
- 125000005907 alkyl ester group Chemical group 0.000 claims description 40
- 150000003839 salts Chemical class 0.000 claims description 34
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 31
- JJWLVOIRVHMVIS-UHFFFAOYSA-O isopropylaminium Chemical compound CC(C)[NH3+] JJWLVOIRVHMVIS-UHFFFAOYSA-O 0.000 claims description 30
- 125000000217 alkyl group Chemical group 0.000 claims description 27
- 239000007788 liquid Substances 0.000 claims description 21
- 125000002091 cationic group Chemical group 0.000 claims description 12
- 125000003277 amino group Chemical group 0.000 claims description 10
- 150000001450 anions Chemical class 0.000 claims description 10
- 239000008247 solid mixture Substances 0.000 claims description 10
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims description 9
- 238000007865 diluting Methods 0.000 claims description 9
- 230000002209 hydrophobic effect Effects 0.000 claims description 9
- 150000003973 alkyl amines Chemical class 0.000 claims description 8
- 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 claims description 7
- 239000005561 Glufosinate Substances 0.000 claims description 7
- ROSDSFDQCJNGOL-UHFFFAOYSA-N Dimethylamine Chemical compound CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 claims description 6
- 239000005645 nematicide Substances 0.000 claims description 6
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 5
- 239000005648 plant growth regulator Substances 0.000 claims description 5
- PVSGXWMWNRGTKE-UHFFFAOYSA-N 5-methyl-2-[4-methyl-5-oxo-4-(propan-2-yl)-4,5-dihydro-1H-imidazol-2-yl]pyridine-3-carboxylic acid Chemical compound N1C(=O)C(C(C)C)(C)N=C1C1=NC=C(C)C=C1C(O)=O PVSGXWMWNRGTKE-UHFFFAOYSA-N 0.000 claims description 4
- 230000007423 decrease Effects 0.000 claims description 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 4
- FBUKVWPVBMHYJY-UHFFFAOYSA-N nonanoic acid Chemical compound CCCCCCCCC(O)=O FBUKVWPVBMHYJY-UHFFFAOYSA-N 0.000 claims description 4
- 238000001556 precipitation Methods 0.000 claims description 4
- 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 claims description 3
- 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 3
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 claims description 3
- 125000003342 alkenyl group Chemical group 0.000 claims description 3
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 3
- 229910052700 potassium Inorganic materials 0.000 claims description 3
- 239000011591 potassium Substances 0.000 claims description 3
- 229910052708 sodium Inorganic materials 0.000 claims description 3
- 239000011734 sodium Substances 0.000 claims description 3
- MZHCENGPTKEIGP-UHFFFAOYSA-N 2-(2,4-dichlorophenoxy)propanoic acid Chemical compound OC(=O)C(C)OC1=CC=C(Cl)C=C1Cl MZHCENGPTKEIGP-UHFFFAOYSA-N 0.000 claims description 2
- 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 claims description 2
- OOLBCHYXZDXLDS-UHFFFAOYSA-N 2-[4-(2,4-dichlorophenoxy)phenoxy]propanoic acid Chemical compound C1=CC(OC(C)C(O)=O)=CC=C1OC1=CC=C(Cl)C=C1Cl OOLBCHYXZDXLDS-UHFFFAOYSA-N 0.000 claims description 2
- 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 claims description 2
- YHKBGVDUSSWOAB-UHFFFAOYSA-N 2-chloro-3-{2-chloro-5-[4-(difluoromethyl)-3-methyl-5-oxo-4,5-dihydro-1H-1,2,4-triazol-1-yl]-4-fluorophenyl}propanoic acid Chemical compound O=C1N(C(F)F)C(C)=NN1C1=CC(CC(Cl)C(O)=O)=C(Cl)C=C1F YHKBGVDUSSWOAB-UHFFFAOYSA-N 0.000 claims description 2
- ABOOPXYCKNFDNJ-UHFFFAOYSA-N 2-{4-[(6-chloroquinoxalin-2-yl)oxy]phenoxy}propanoic acid Chemical compound C1=CC(OC(C)C(O)=O)=CC=C1OC1=CN=C(C=C(Cl)C=C2)C2=N1 ABOOPXYCKNFDNJ-UHFFFAOYSA-N 0.000 claims description 2
- UPMXNNIRAGDFEH-UHFFFAOYSA-N 3,5-dibromo-4-hydroxybenzonitrile Chemical compound OC1=C(Br)C=C(C#N)C=C1Br UPMXNNIRAGDFEH-UHFFFAOYSA-N 0.000 claims description 2
- CTSLUCNDVMMDHG-UHFFFAOYSA-N 5-bromo-3-(butan-2-yl)-6-methylpyrimidine-2,4(1H,3H)-dione Chemical compound CCC(C)N1C(=O)NC(C)=C(Br)C1=O CTSLUCNDVMMDHG-UHFFFAOYSA-N 0.000 claims description 2
- 239000005476 Bentazone Substances 0.000 claims description 2
- 239000005489 Bromoxynil Substances 0.000 claims description 2
- HSSBORCLYSCBJR-UHFFFAOYSA-N Chloramben Chemical compound NC1=CC(Cl)=CC(C(O)=O)=C1Cl HSSBORCLYSCBJR-UHFFFAOYSA-N 0.000 claims description 2
- 239000005500 Clopyralid Substances 0.000 claims description 2
- 239000005504 Dicamba Substances 0.000 claims description 2
- 239000005506 Diclofop Substances 0.000 claims description 2
- 239000005566 Imazamox Substances 0.000 claims description 2
- 239000005981 Imazaquin Substances 0.000 claims description 2
- 239000005595 Picloram Substances 0.000 claims description 2
- 239000005627 Triclopyr Substances 0.000 claims description 2
- NUFNQYOELLVIPL-UHFFFAOYSA-N acifluorfen Chemical group C1=C([N+]([O-])=O)C(C(=O)O)=CC(OC=2C(=CC(=CC=2)C(F)(F)F)Cl)=C1 NUFNQYOELLVIPL-UHFFFAOYSA-N 0.000 claims description 2
- 125000002723 alicyclic group Chemical group 0.000 claims description 2
- 125000003118 aryl group Chemical group 0.000 claims description 2
- VGPYEHKOIGNJKV-UHFFFAOYSA-N asulam Chemical compound COC(=O)NS(=O)(=O)C1=CC=C(N)C=C1 VGPYEHKOIGNJKV-UHFFFAOYSA-N 0.000 claims description 2
- ZOMSMJKLGFBRBS-UHFFFAOYSA-N bentazone Chemical compound C1=CC=C2NS(=O)(=O)N(C(C)C)C(=O)C2=C1 ZOMSMJKLGFBRBS-UHFFFAOYSA-N 0.000 claims description 2
- CNBGNNVCVSKAQZ-UHFFFAOYSA-N benzidamine Natural products C12=CC=CC=C2C(OCCCN(C)C)=NN1CC1=CC=CC=C1 CNBGNNVCVSKAQZ-UHFFFAOYSA-N 0.000 claims description 2
- GINJFDRNADDBIN-FXQIFTODSA-N bilanafos Chemical compound OC(=O)[C@H](C)NC(=O)[C@H](C)NC(=O)[C@@H](N)CCP(C)(O)=O GINJFDRNADDBIN-FXQIFTODSA-N 0.000 claims description 2
- HUBANNPOLNYSAD-UHFFFAOYSA-N clopyralid Chemical compound OC(=O)C1=NC(Cl)=CC=C1Cl HUBANNPOLNYSAD-UHFFFAOYSA-N 0.000 claims description 2
- IWEDIXLBFLAXBO-UHFFFAOYSA-N dicamba Chemical compound COC1=C(Cl)C=CC(Cl)=C1C(O)=O IWEDIXLBFLAXBO-UHFFFAOYSA-N 0.000 claims description 2
- BGZZWXTVIYUUEY-UHFFFAOYSA-N fomesafen Chemical compound C1=C([N+]([O-])=O)C(C(=O)NS(=O)(=O)C)=CC(OC=2C(=CC(=CC=2)C(F)(F)F)Cl)=C1 BGZZWXTVIYUUEY-UHFFFAOYSA-N 0.000 claims description 2
- 125000000743 hydrocarbylene group Chemical group 0.000 claims description 2
- NDNKHWUXXOFHTD-UHFFFAOYSA-N metizoline Chemical compound CC=1SC2=CC=CC=C2C=1CC1=NCCN1 NDNKHWUXXOFHTD-UHFFFAOYSA-N 0.000 claims description 2
- 229960002939 metizoline Drugs 0.000 claims description 2
- LNOPIUAQISRISI-UHFFFAOYSA-N n'-hydroxy-2-propan-2-ylsulfonylethanimidamide Chemical compound CC(C)S(=O)(=O)CC(N)=NO LNOPIUAQISRISI-UHFFFAOYSA-N 0.000 claims description 2
- NQQVFXUMIDALNH-UHFFFAOYSA-N picloram Chemical compound NC1=C(Cl)C(Cl)=NC(C(O)=O)=C1Cl NQQVFXUMIDALNH-UHFFFAOYSA-N 0.000 claims description 2
- 229920001451 polypropylene glycol Polymers 0.000 claims description 2
- FFSSWMQPCJRCRV-UHFFFAOYSA-N quinclorac Chemical compound ClC1=CN=C2C(C(=O)O)=C(Cl)C=CC2=C1 FFSSWMQPCJRCRV-UHFFFAOYSA-N 0.000 claims description 2
- REEQLXCGVXDJSQ-UHFFFAOYSA-N trichlopyr Chemical compound OC(=O)COC1=NC(Cl)=C(Cl)C=C1Cl REEQLXCGVXDJSQ-UHFFFAOYSA-N 0.000 claims description 2
- QYPPRTNMGCREIM-UHFFFAOYSA-N methylarsonic acid Chemical compound C[As](O)(O)=O QYPPRTNMGCREIM-UHFFFAOYSA-N 0.000 claims 2
- WNTGYJSOUMFZEP-UHFFFAOYSA-N 2-(4-chloro-2-methylphenoxy)propanoic acid Chemical compound OC(=O)C(C)OC1=CC=C(Cl)C=C1C WNTGYJSOUMFZEP-UHFFFAOYSA-N 0.000 claims 1
- GOCUAJYOYBLQRH-UHFFFAOYSA-N 2-(4-{[3-chloro-5-(trifluoromethyl)pyridin-2-yl]oxy}phenoxy)propanoic acid Chemical compound C1=CC(OC(C)C(O)=O)=CC=C1OC1=NC=C(C(F)(F)F)C=C1Cl GOCUAJYOYBLQRH-UHFFFAOYSA-N 0.000 claims 1
- YUVKUEAFAVKILW-UHFFFAOYSA-N 2-(4-{[5-(trifluoromethyl)pyridin-2-yl]oxy}phenoxy)propanoic acid Chemical compound C1=CC(OC(C)C(O)=O)=CC=C1OC1=CC=C(C(F)(F)F)C=N1 YUVKUEAFAVKILW-UHFFFAOYSA-N 0.000 claims 1
- GQQIAHNFBAFBCS-UHFFFAOYSA-N 2-[2-chloro-5-(1,3-dioxo-4,5,6,7-tetrahydroisoindol-2-yl)-4-fluorophenoxy]acetic acid Chemical compound C1=C(Cl)C(OCC(=O)O)=CC(N2C(C3=C(CCCC3)C2=O)=O)=C1F GQQIAHNFBAFBCS-UHFFFAOYSA-N 0.000 claims 1
- MPPOHAUSNPTFAJ-UHFFFAOYSA-N 2-[4-[(6-chloro-1,3-benzoxazol-2-yl)oxy]phenoxy]propanoic acid Chemical compound C1=CC(OC(C)C(O)=O)=CC=C1OC1=NC2=CC=C(Cl)C=C2O1 MPPOHAUSNPTFAJ-UHFFFAOYSA-N 0.000 claims 1
- YQVMVCCFZCMYQB-UHFFFAOYSA-N Flamprop Chemical compound C=1C=C(F)C(Cl)=CC=1N(C(C)C(O)=O)C(=O)C1=CC=CC=C1 YQVMVCCFZCMYQB-UHFFFAOYSA-N 0.000 claims 1
- DHAHEVIQIYRFRG-UHFFFAOYSA-N Fluoroglycofen Chemical compound C1=C([N+]([O-])=O)C(C(=O)OCC(=O)O)=CC(OC=2C(=CC(=CC=2)C(F)(F)F)Cl)=C1 DHAHEVIQIYRFRG-UHFFFAOYSA-N 0.000 claims 1
- 101001013832 Homo sapiens Mitochondrial peptide methionine sulfoxide reductase Proteins 0.000 claims 1
- XVOKUMIPKHGGTN-UHFFFAOYSA-N Imazethapyr Chemical compound OC(=O)C1=CC(CC)=CN=C1C1=NC(C)(C(C)C)C(=O)N1 XVOKUMIPKHGGTN-UHFFFAOYSA-N 0.000 claims 1
- 102100031767 Mitochondrial peptide methionine sulfoxide reductase Human genes 0.000 claims 1
- OTSAMNSACVKIOJ-UHFFFAOYSA-N azane;carbamoyl(ethoxy)phosphinic acid Chemical compound [NH4+].CCOP([O-])(=O)C(N)=O OTSAMNSACVKIOJ-UHFFFAOYSA-N 0.000 claims 1
- QZXCCPZJCKEPSA-UHFFFAOYSA-N chlorfenac Chemical compound OC(=O)CC1=C(Cl)C=CC(Cl)=C1Cl QZXCCPZJCKEPSA-UHFFFAOYSA-N 0.000 claims 1
- NRXQIUSYPAHGNM-UHFFFAOYSA-N ioxynil Chemical compound OC1=C(I)C=C(C#N)C=C1I NRXQIUSYPAHGNM-UHFFFAOYSA-N 0.000 claims 1
- 150000003242 quaternary ammonium salts Chemical class 0.000 claims 1
- 238000012876 topography Methods 0.000 claims 1
- 230000004913 activation Effects 0.000 abstract description 3
- 239000002671 adjuvant Substances 0.000 abstract description 3
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract description 2
- 125000000204 (C2-C4) acyl group Chemical group 0.000 abstract 1
- 235000008504 concentrate Nutrition 0.000 description 86
- 241000894007 species Species 0.000 description 33
- 230000000052 comparative effect Effects 0.000 description 32
- 239000004615 ingredient Substances 0.000 description 28
- 238000010561 standard procedure Methods 0.000 description 26
- 239000005590 Oxyfluorfen Substances 0.000 description 25
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 25
- 239000000945 filler Substances 0.000 description 25
- OQMBBFQZGJFLBU-UHFFFAOYSA-N Oxyfluorfen Chemical compound C1=C([N+]([O-])=O)C(OCC)=CC(OC=2C(=CC(=CC=2)C(F)(F)F)Cl)=C1 OQMBBFQZGJFLBU-UHFFFAOYSA-N 0.000 description 24
- IIZPXYDJLKNOIY-JXPKJXOSSA-N 1-palmitoyl-2-arachidonoyl-sn-glycero-3-phosphocholine Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@H](COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCC\C=C/C\C=C/C\C=C/C\C=C/CCCCC IIZPXYDJLKNOIY-JXPKJXOSSA-N 0.000 description 22
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- QMMJWQMCMRUYTG-UHFFFAOYSA-N 1,2,4,5-tetrachloro-3-(trifluoromethyl)benzene Chemical compound FC(F)(F)C1=C(Cl)C(Cl)=CC(Cl)=C1Cl QMMJWQMCMRUYTG-UHFFFAOYSA-N 0.000 description 14
- 244000058871 Echinochloa crus-galli Species 0.000 description 14
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- PDYXIVPKOMYDOK-UHFFFAOYSA-N Glyphosate-monoammonium Chemical compound [NH4+].OC(=O)CNCP(O)([O-])=O PDYXIVPKOMYDOK-UHFFFAOYSA-N 0.000 description 9
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- 125000001117 oleyl 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])=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 description 5
- 125000000913 palmityl 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])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 5
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- 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
- 230000035790 physiological processes and functions Effects 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920000151 polyglycol Polymers 0.000 description 1
- 239000010695 polyglycol Substances 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 230000008092 positive effect Effects 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 230000035755 proliferation Effects 0.000 description 1
- ISEUFVQQFVOBCY-UHFFFAOYSA-N prometon Chemical compound COC1=NC(NC(C)C)=NC(NC(C)C)=N1 ISEUFVQQFVOBCY-UHFFFAOYSA-N 0.000 description 1
- MFOUDYKPLGXPGO-UHFFFAOYSA-N propachlor Chemical compound ClCC(=O)N(C(C)C)C1=CC=CC=C1 MFOUDYKPLGXPGO-UHFFFAOYSA-N 0.000 description 1
- LFULEKSKNZEWOE-UHFFFAOYSA-N propanil Chemical compound CCC(=O)NC1=CC=C(Cl)C(Cl)=C1 LFULEKSKNZEWOE-UHFFFAOYSA-N 0.000 description 1
- WJNRPILHGGKWCK-UHFFFAOYSA-N propazine Chemical compound CC(C)NC1=NC(Cl)=NC(NC(C)C)=N1 WJNRPILHGGKWCK-UHFFFAOYSA-N 0.000 description 1
- VXPLXMJHHKHSOA-UHFFFAOYSA-N propham Chemical compound CC(C)OC(=O)NC1=CC=CC=C1 VXPLXMJHHKHSOA-UHFFFAOYSA-N 0.000 description 1
- NQLVQOSNDJXLKG-UHFFFAOYSA-N prosulfocarb Chemical compound CCCN(CCC)C(=O)SCC1=CC=CC=C1 NQLVQOSNDJXLKG-UHFFFAOYSA-N 0.000 description 1
- USSIUIGPBLPCDF-KEBDBYFISA-N pyriminobac-methyl Chemical group CO\N=C(/C)C1=CC=CC(OC=2N=C(OC)C=C(OC)N=2)=C1C(=O)OC USSIUIGPBLPCDF-KEBDBYFISA-N 0.000 description 1
- 125000001453 quaternary ammonium group Chemical group 0.000 description 1
- BACHBFVBHLGWSL-JTQLQIEISA-N rac-diclofop methyl Natural products C1=CC(O[C@@H](C)C(=O)OC)=CC=C1OC1=CC=C(Cl)C=C1Cl BACHBFVBHLGWSL-JTQLQIEISA-N 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 230000010076 replication Effects 0.000 description 1
- 230000033458 reproduction Effects 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 235000009566 rice Nutrition 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
- 150000004671 saturated fatty acids Chemical class 0.000 description 1
- 150000003333 secondary alcohols Chemical class 0.000 description 1
- SBEQWOXEGHQIMW-UHFFFAOYSA-N silicon Chemical compound [Si].[Si] SBEQWOXEGHQIMW-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
- 159000000000 sodium salts Chemical class 0.000 description 1
- 238000009331 sowing Methods 0.000 description 1
- 239000003549 soybean oil Substances 0.000 description 1
- 235000012424 soybean oil Nutrition 0.000 description 1
- 238000004611 spectroscopical analysis Methods 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 230000000087 stabilizing effect Effects 0.000 description 1
- 229940010735 steareth-12 Drugs 0.000 description 1
- 229940080728 steareth-30 Drugs 0.000 description 1
- 230000004936 stimulating effect Effects 0.000 description 1
- ADNPLDHMAVUMIW-CUZNLEPHSA-N substance P Chemical compound C([C@@H](C(=O)NCC(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCSC)C(N)=O)NC(=O)[C@H](CC=1C=CC=CC=1)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H]1N(CCC1)C(=O)[C@H](CCCCN)NC(=O)[C@H]1N(CCC1)C(=O)[C@@H](N)CCCN=C(N)N)C1=CC=CC=C1 ADNPLDHMAVUMIW-CUZNLEPHSA-N 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
- FZMKKCQHDROFNI-UHFFFAOYSA-N sulfometuron Chemical compound CC1=CC(C)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2)C(O)=O)=N1 FZMKKCQHDROFNI-UHFFFAOYSA-N 0.000 description 1
- RWSOTUBLDIXVET-UHFFFAOYSA-O sulfonium Chemical compound [SH3+] RWSOTUBLDIXVET-UHFFFAOYSA-O 0.000 description 1
- 239000000375 suspending agent Substances 0.000 description 1
- 230000008961 swelling Effects 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
- 235000012976 tarts Nutrition 0.000 description 1
- RJKCKKDSSSRYCB-UHFFFAOYSA-N tebutam Chemical compound CC(C)(C)C(=O)N(C(C)C)CC1=CC=CC=C1 RJKCKKDSSSRYCB-UHFFFAOYSA-N 0.000 description 1
- BCQMBFHBDZVHKU-UHFFFAOYSA-N terbumeton Chemical compound CCNC1=NC(NC(C)(C)C)=NC(OC)=N1 BCQMBFHBDZVHKU-UHFFFAOYSA-N 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
- 150000003512 tertiary amines Chemical class 0.000 description 1
- 230000001225 therapeutic effect Effects 0.000 description 1
- 239000002562 thickening agent Substances 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
- SRVJKTDHMYAMHA-WUXMJOGZSA-N thioacetazone Chemical compound CC(=O)NC1=CC=C(\C=N\NC(N)=S)C=C1 SRVJKTDHMYAMHA-WUXMJOGZSA-N 0.000 description 1
- 229960003231 thioacetazone Drugs 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- 230000005945 translocation Effects 0.000 description 1
- XOPFESVZMSQIKC-UHFFFAOYSA-N triasulfuron Chemical compound COC1=NC(C)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2)OCCCl)=N1 XOPFESVZMSQIKC-UHFFFAOYSA-N 0.000 description 1
- ZSDSQXJSNMTJDA-UHFFFAOYSA-N trifluralin Chemical compound CCCN(CCC)C1=C([N+]([O-])=O)C=C(C(F)(F)F)C=C1[N+]([O-])=O ZSDSQXJSNMTJDA-UHFFFAOYSA-N 0.000 description 1
- AKTQJCBOGPBERP-UHFFFAOYSA-N triflusulfuron Chemical compound FC(F)(F)COC1=NC(N(C)C)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2C)C(O)=O)=N1 AKTQJCBOGPBERP-UHFFFAOYSA-N 0.000 description 1
- UFTFJSFQGQCHQW-UHFFFAOYSA-N triformin Chemical compound O=COCC(OC=O)COC=O UFTFJSFQGQCHQW-UHFFFAOYSA-N 0.000 description 1
- 150000004670 unsaturated fatty acids Chemical class 0.000 description 1
- 235000021122 unsaturated fatty acids Nutrition 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 230000000007 visual effect Effects 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
- A01N25/30—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests characterised by the surfactants
-
- 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
- A01N57/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds
- A01N57/18—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-carbon bonds
- A01N57/20—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-carbon bonds containing acyclic or cycloaliphatic radicals
Landscapes
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- Agronomy & Crop Science (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Toxicology (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US13075699P | 1999-04-23 | 1999-04-23 | |
PCT/US2000/008907 WO2000064258A1 (en) | 1999-04-23 | 2000-04-03 | Method of enhancing biological effectiveness of plant treatment compositions |
Publications (1)
Publication Number | Publication Date |
---|---|
UA72760C2 true UA72760C2 (en) | 2005-04-15 |
Family
ID=22446174
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
UA2001117999A UA72760C2 (en) | 1999-04-23 | 2000-03-04 | Method to treat plant foliage |
UA2001118000A UA72761C2 (en) | 1999-04-23 | 2000-03-04 | Compositions and method of eliminating plant growth or controlling thereof |
Family Applications After (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
UA2001118000A UA72761C2 (en) | 1999-04-23 | 2000-03-04 | Compositions and method of eliminating plant growth or controlling thereof |
Country Status (26)
Country | Link |
---|---|
EP (2) | EP1173059B1 (pt) |
JP (2) | JP5030332B2 (pt) |
KR (2) | KR20020008844A (pt) |
CN (2) | CN1356869A (pt) |
AR (3) | AR023559A1 (pt) |
AT (2) | ATE276657T1 (pt) |
AU (3) | AU4192100A (pt) |
BR (2) | BR0010657B1 (pt) |
CA (2) | CA2369636C (pt) |
CO (1) | CO5241274A1 (pt) |
CZ (2) | CZ20013764A3 (pt) |
DE (2) | DE60014105T2 (pt) |
DK (1) | DK1173059T3 (pt) |
EA (2) | EA200101120A1 (pt) |
ES (2) | ES2251998T3 (pt) |
GT (1) | GT200000047A (pt) |
HU (2) | HUP0201138A3 (pt) |
MX (2) | MXPA01010763A (pt) |
MY (2) | MY130215A (pt) |
NZ (2) | NZ514816A (pt) |
PH (2) | PH12000000991B1 (pt) |
PL (2) | PL201290B1 (pt) |
SK (2) | SK15002001A3 (pt) |
UA (2) | UA72760C2 (pt) |
WO (3) | WO2000064256A1 (pt) |
ZA (2) | ZA200108684B (pt) |
Families Citing this family (34)
Publication number | Priority date | Publication date | Assignee | Title |
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CN1192707C (zh) | 1999-10-26 | 2005-03-16 | 陶氏益农有限责任公司 | 除草剂的浓悬浮剂 |
MY158895A (en) * | 2000-05-19 | 2016-11-30 | Monsanto Technology Llc | Potassium glyphosate formulations |
DE10063960A1 (de) * | 2000-12-20 | 2002-06-27 | Aventis Cropscience Gmbh | Herbizide Mittel |
MXPA03010265A (es) * | 2001-05-08 | 2004-03-10 | Monsanto Europe Sa | Composiciones de glifosato y su uso. |
WO2003051117A1 (fr) * | 2001-12-19 | 2003-06-26 | Nihon Nohyaku Co., Ltd. | Composition herbicide et procede d'utilisation |
AU2003268696A1 (en) * | 2002-09-30 | 2004-04-19 | Bayer Cropscience | Herbicidal mixed liquid formulation |
US20050026781A1 (en) | 2003-04-22 | 2005-02-03 | Monsanto Technology Llc | Herbicidal compositions containing glyphosate and a pyridine analog |
PT1651048T (pt) * | 2003-08-04 | 2016-09-26 | Dow Agrosciences Llc | Formulações herbicidas de glifosato com elevada concentração, de baixa viscosidade |
US20050101488A1 (en) * | 2003-10-21 | 2005-05-12 | Sumitomo Chemical Company, Limited | Herbicidal composition |
EP1722634B2 (en) | 2004-03-10 | 2020-09-02 | Monsanto Technology LLC | Herbicidal compositions containing n-phosphonomethyl glycine and an auxin herbicide |
CA2472806A1 (en) | 2004-05-18 | 2005-11-18 | Petro-Canada | Compositions and methods for treating turf insect pests and diseases such as fungal infestations |
JP2006056784A (ja) * | 2004-08-17 | 2006-03-02 | Sankyo Agro Kk | 安定化された水性除草剤組成物 |
AU2005286666B2 (en) | 2004-09-23 | 2011-05-19 | Akzo Nobel N.V. | Alkoxylated alkylamines / alkyl ether amines with peaked distribution |
MY148811A (en) * | 2004-09-27 | 2013-05-31 | Kao Corp | Herbicide composition, herbicide-enhancer and enhancing method |
JP2006117650A (ja) * | 2004-09-27 | 2006-05-11 | Kao Corp | 除草剤組成物 |
TWI451842B (zh) | 2005-07-04 | 2014-09-11 | Sumitomo Chemical Co | 殺蟲劑組成物 |
SG170758A1 (en) * | 2006-03-23 | 2011-05-30 | Akzo Nobel Nv | Alkoxylated alkylamines or alkyl ether amines with peaked distribution |
US9357768B2 (en) | 2006-10-05 | 2016-06-07 | Suncor Energy Inc. | Herbicidal composition with increased herbicidal efficacy |
WO2008069826A1 (en) | 2006-12-06 | 2008-06-12 | Akzo Nobel N.V. | Compatibility agents for herbicidal formulations comprising 2,4-(dichlorophenoxy) acetic acid salts |
CA2672151A1 (en) | 2006-12-06 | 2008-06-12 | Akzo Nobel N.V. | Alkylamidopropyl dialkylamine surfactants as adjuvants |
AU2008270253B2 (en) * | 2007-07-05 | 2013-09-19 | Akzo Nobel Chemicals International B.V. | Alkoxylated asymmetric alkylamine surfactants as adjuvants |
KR20110025225A (ko) | 2008-06-26 | 2011-03-09 | 선코 에너지 인코포레이티드 | 안료를 가진 개선된 터프그래스 살균 제제 |
BRPI0912933B1 (pt) * | 2008-08-19 | 2016-11-08 | Akzo Nobel Nv | formulação de glifosato espessada, e, método de espessamento de uma formulação de glifosato |
EP2266394A1 (en) | 2009-06-17 | 2010-12-29 | Cognis IP Management GmbH | Non-aqueous agricultural compositions |
NZ609203A (en) | 2010-09-09 | 2014-10-31 | Suncor Energy Inc | Synergistic paraffinic oil and boscalid fungicides |
ES2735285T3 (es) | 2011-06-03 | 2019-12-17 | Suncor Energy Inc | Emulsiones de aceite parafínico en agua para controlar la infección de plantas de cultivo por patógenos fúngicos |
BR112014010034B1 (pt) | 2011-10-26 | 2019-04-24 | Monsanto Technology Llc | Sais herbicidas de auxina, mistura de aplicação herbicida compreendendo os mesmos para uso na eliminação e controle do crescimento de plantas indesejadas,bem como métodos de controle de plantas indesejadas e de plantas suscetíveis ao herbicida de auxina |
UA116536C2 (uk) * | 2012-03-23 | 2018-04-10 | ДАУ АГРОСАЙЄНСІЗ ЕлЕлСі | Водні концентрати гербіцидів, що містять складні алкілові ефіри жирних кислот, аміди жирних кислот або складні ефіри тригліцеридів і жирних кислот, і способи їх застосування |
KR101367258B1 (ko) * | 2012-04-17 | 2014-02-27 | 인바이오 주식회사 | 속효성과 지효성을 동시에 갖는 제초제 |
AR091268A1 (es) | 2012-06-04 | 2015-01-21 | Monsanto Technology Llc | Composiciones herbicidas concentradas acuosas que contienen sales de glifosato y sales de dicamba |
TR201815726T4 (tr) | 2013-02-27 | 2018-11-21 | Monsanto Technology Llc | Geliştirilmiş bir uçuculuğa sahip glifosat ve dikamba tank karışımlar. |
WO2020008940A1 (ja) * | 2018-07-05 | 2020-01-09 | 花王株式会社 | 除草剤組成物 |
JP7321761B2 (ja) * | 2018-07-05 | 2023-08-07 | 花王株式会社 | 除草剤組成物 |
CN112998002A (zh) * | 2021-03-06 | 2021-06-22 | 通辽市农业科学研究院 | 一种荞麦田的除草方法 |
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AU3148384A (en) * | 1983-10-28 | 1985-05-02 | Chevron Research Company | Glyphosate type herbicide plus oxyfluorfen |
US5206021A (en) | 1988-05-09 | 1993-04-27 | Rhone-Poulenc Ag Company | Stabilized oil-in-water emulsions or suspoemulsions containing pesticidal substances in both oil and water phases |
KR920002217B1 (ko) | 1988-06-14 | 1992-03-20 | 몬산토 캄파니 | 개선된 제초제와 그 이용 |
EP0448538B1 (en) | 1990-03-15 | 1997-01-02 | Monsanto Company | Improved glyphosate formulations |
GB2267825B (en) * | 1992-05-26 | 1995-08-30 | Dowelanco | Herbicidal aqueous-based microemulsion compositions |
ZA936170B (en) | 1992-08-24 | 1994-06-01 | Monsanto Co | Herbicidal compositions |
EP0617894B1 (en) * | 1993-04-02 | 1998-12-16 | Monsanto Europe S.A./N.V. | Liquid concentrated herbicidal glyphosate compositions |
GB9412722D0 (en) * | 1994-06-24 | 1994-08-17 | Zeneca Ltd | Herbicidal composition |
JP3799669B2 (ja) * | 1996-07-29 | 2006-07-19 | 日産化学工業株式会社 | 除草剤組成物 |
US5821195A (en) * | 1996-08-16 | 1998-10-13 | Monsanto Company | Sequential application method for enhancing glyphosate herbicidal effectiveness with reduced antagonism |
CA2269725C (en) * | 1996-10-25 | 2010-01-05 | Monsanto Company | Composition and method for treating plants with exogenous chemicals |
-
2000
- 2000-03-04 UA UA2001117999A patent/UA72760C2/uk unknown
- 2000-03-04 UA UA2001118000A patent/UA72761C2/uk unknown
- 2000-04-03 AU AU41921/00A patent/AU4192100A/en not_active Abandoned
- 2000-04-03 HU HU0201138A patent/HUP0201138A3/hu unknown
- 2000-04-03 AU AU46418/00A patent/AU776887B2/en not_active Expired
- 2000-04-03 EA EA200101120A patent/EA200101120A1/ru unknown
- 2000-04-03 JP JP2000613261A patent/JP5030332B2/ja not_active Expired - Lifetime
- 2000-04-03 CZ CZ20013764A patent/CZ20013764A3/cs unknown
- 2000-04-03 PL PL351838A patent/PL201290B1/pl unknown
- 2000-04-03 SK SK1500-2001A patent/SK15002001A3/sk unknown
- 2000-04-03 AT AT00925888T patent/ATE276657T1/de not_active IP Right Cessation
- 2000-04-03 DK DK00928138T patent/DK1173059T3/da active
- 2000-04-03 EP EP00928138A patent/EP1173059B1/en not_active Expired - Lifetime
- 2000-04-03 EP EP00925888A patent/EP1202623B1/en not_active Expired - Lifetime
- 2000-04-03 SK SK1502-2001A patent/SK15022001A3/sk unknown
- 2000-04-03 BR BRPI0010657-7A patent/BR0010657B1/pt active IP Right Grant
- 2000-04-03 CN CN00809186A patent/CN1356869A/zh active Pending
- 2000-04-03 ES ES00928138T patent/ES2251998T3/es not_active Expired - Lifetime
- 2000-04-03 AU AU44510/00A patent/AU776036B2/en not_active Expired
- 2000-04-03 CA CA002369636A patent/CA2369636C/en not_active Expired - Lifetime
- 2000-04-03 WO PCT/US2000/008763 patent/WO2000064256A1/en not_active Application Discontinuation
- 2000-04-03 EA EA200101123A patent/EA200101123A1/ru unknown
- 2000-04-03 BR BR0010656-9A patent/BR0010656A/pt not_active Application Discontinuation
- 2000-04-03 NZ NZ514816A patent/NZ514816A/en not_active IP Right Cessation
- 2000-04-03 CA CA002369738A patent/CA2369738C/en not_active Expired - Lifetime
- 2000-04-03 WO PCT/US2000/008843 patent/WO2000064257A1/en active Application Filing
- 2000-04-03 AT AT00928138T patent/ATE308880T1/de not_active IP Right Cessation
- 2000-04-03 CN CN00809194A patent/CN1356870A/zh active Pending
- 2000-04-03 ES ES00925888T patent/ES2228507T3/es not_active Expired - Lifetime
- 2000-04-03 NZ NZ514817A patent/NZ514817A/en not_active IP Right Cessation
- 2000-04-03 CZ CZ20013765A patent/CZ20013765A3/cs unknown
- 2000-04-03 JP JP2000613259A patent/JP2002542266A/ja active Pending
- 2000-04-03 PL PL351840A patent/PL199160B1/pl unknown
- 2000-04-03 WO PCT/US2000/008907 patent/WO2000064258A1/en active IP Right Grant
- 2000-04-03 DE DE60014105T patent/DE60014105T2/de not_active Expired - Lifetime
- 2000-04-03 HU HU0201106A patent/HUP0201106A3/hu unknown
- 2000-04-03 KR KR1020017013525A patent/KR20020008844A/ko not_active Application Discontinuation
- 2000-04-03 DE DE60023872T patent/DE60023872T2/de not_active Expired - Lifetime
- 2000-04-03 KR KR1020017013524A patent/KR20020008393A/ko not_active Application Discontinuation
- 2000-04-18 GT GT200000047A patent/GT200000047A/es unknown
- 2000-04-19 AR ARP000101859A patent/AR023559A1/es unknown
- 2000-04-19 PH PH12000000991A patent/PH12000000991B1/en unknown
- 2000-04-19 AR ARP000101857A patent/AR023557A1/es active IP Right Grant
- 2000-04-19 PH PH12000000990A patent/PH12000000990B1/en unknown
- 2000-04-19 AR ARP000101858A patent/AR023558A1/es active IP Right Grant
- 2000-04-19 CO CO00029094A patent/CO5241274A1/es not_active Application Discontinuation
- 2000-04-21 MY MYPI20001701A patent/MY130215A/en unknown
- 2000-04-21 MY MYPI20001703A patent/MY126950A/en unknown
-
2001
- 2001-10-22 ZA ZA200108684A patent/ZA200108684B/xx unknown
- 2001-10-22 ZA ZA200108687A patent/ZA200108687B/xx unknown
- 2001-10-23 MX MXPA01010763 patent/MXPA01010763A/es active IP Right Grant
- 2001-10-23 MX MXPA01010762 patent/MXPA01010762A/es active IP Right Grant
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