SK7082001A3 - Compact storage and shipping system for glyphosate herbicide - Google Patents

Compact storage and shipping system for glyphosate herbicide Download PDF

Info

Publication number: SK7082001A3
Authority: SK; Slovakia
Prior art keywords: glyphosate; salt; solution; storage; concentration
Prior art date: 1998-11-23

Application number

SK708-2001A

Other languages

English (en)

Slovak (sk)

Inventor

Daniel R Wright

Original Assignee

Monsanto Co

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.)

1998-11-23

Filing date

1999-11-19

Publication date

2002-05-09

Family has litigation

First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=22328088&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=SK7082001(A3) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.

1999-11-19 Application filed by Monsanto Co filed Critical Monsanto Co

2002-05-09 Publication of SK7082001A3 publication Critical patent/SK7082001A3/sk

Links

XDDAORKBJWWYJS-UHFFFAOYSA-N glyphosate Chemical compound OC(=O)CNCP(O)(O)=O XDDAORKBJWWYJS-UHFFFAOYSA-N 0.000 title claims abstract description 298
239000005562 Glyphosate Substances 0.000 title claims abstract description 245
229940097068 glyphosate Drugs 0.000 title claims abstract description 245
238000003860 storage Methods 0.000 title claims abstract description 93
230000002363 herbicidal effect Effects 0.000 title claims abstract description 52
239000004009 herbicide Substances 0.000 title claims abstract description 48
239000000203 mixture Substances 0.000 claims abstract description 135
150000003839 salts Chemical class 0.000 claims abstract description 127
239000002253 acid Substances 0.000 claims abstract description 39
239000011591 potassium Substances 0.000 claims abstract description 22
229910052700 potassium Inorganic materials 0.000 claims abstract description 22
ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 claims abstract description 18
239000004094 surface-active agent Substances 0.000 claims description 147
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 32
238000000034 method Methods 0.000 claims description 12
238000011049 filling Methods 0.000 claims description 9
238000011068 loading method Methods 0.000 claims description 9
239000000654 additive Substances 0.000 claims description 8
150000001768 cations Chemical class 0.000 claims description 5
239000012736 aqueous medium Substances 0.000 claims description 4
238000002425 crystallisation Methods 0.000 claims description 4
230000008025 crystallization Effects 0.000 claims description 4
239000006185 dispersion Substances 0.000 claims description 4
238000005191 phase separation Methods 0.000 claims description 4
150000003109 potassium Chemical class 0.000 claims description 4
239000000243 solution Substances 0.000 abstract description 54
239000012266 salt solution Substances 0.000 abstract description 43
239000007864 aqueous solution Substances 0.000 abstract description 30
JJWLVOIRVHMVIS-UHFFFAOYSA-N isopropylamine Chemical class CC(C)N JJWLVOIRVHMVIS-UHFFFAOYSA-N 0.000 abstract description 5
230000005484 gravity Effects 0.000 abstract 1
JJWLVOIRVHMVIS-UHFFFAOYSA-O isopropylaminium Chemical compound CC(C)[NH3+] JJWLVOIRVHMVIS-UHFFFAOYSA-O 0.000 description 68
-1 glyphosate TMS salt Chemical class 0.000 description 52
230000008901 benefit Effects 0.000 description 29
229920003171 Poly (ethylene oxide) Polymers 0.000 description 20
ZEKANFGSDXODPD-UHFFFAOYSA-N glyphosate-isopropylammonium Chemical compound CC(C)N.OC(=O)CNCP(O)(O)=O ZEKANFGSDXODPD-UHFFFAOYSA-N 0.000 description 20
239000000047 product Substances 0.000 description 17
229910052739 hydrogen Inorganic materials 0.000 description 14
239000001257 hydrogen Substances 0.000 description 14
125000000129 anionic group Chemical group 0.000 description 12
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 11
239000013078 crystal Substances 0.000 description 11
239000004215 Carbon black (E152) Substances 0.000 description 10
229930195733 hydrocarbon Natural products 0.000 description 10
239000007788 liquid Substances 0.000 description 10
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 10
125000006353 oxyethylene group Chemical group 0.000 description 10
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 9
235000008504 concentrate Nutrition 0.000 description 9
239000012141 concentrate Substances 0.000 description 9
230000002209 hydrophobic effect Effects 0.000 description 9
239000000575 pesticide Substances 0.000 description 9
125000004432 carbon atom Chemical group C* 0.000 description 8
238000002360 preparation method Methods 0.000 description 8
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 8
239000004480 active ingredient Substances 0.000 description 7
239000013543 active substance Substances 0.000 description 7
125000001931 aliphatic group Chemical group 0.000 description 7
125000000217 alkyl group Chemical group 0.000 description 7
125000003277 amino group Chemical group 0.000 description 7
239000004615 ingredient Substances 0.000 description 7
238000005086 pumping Methods 0.000 description 7
229920006395 saturated elastomer Polymers 0.000 description 7
VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 6
241000196324 Embryophyta Species 0.000 description 6
206010015946 Eye irritation Diseases 0.000 description 6
231100000013 eye irritation Toxicity 0.000 description 6
NRZWQKGABZFFKE-UHFFFAOYSA-N trimethylsulfonium Chemical class C[S+](C)C NRZWQKGABZFFKE-UHFFFAOYSA-N 0.000 description 6
QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 5
150000003973 alkyl amines Chemical class 0.000 description 5
150000001450 anions Chemical class 0.000 description 5
HUBANNPOLNYSAD-UHFFFAOYSA-N clopyralid Chemical compound OC(=O)C1=NC(Cl)=CC=C1Cl HUBANNPOLNYSAD-UHFFFAOYSA-N 0.000 description 5
230000000052 comparative effect Effects 0.000 description 5
238000004519 manufacturing process Methods 0.000 description 5
XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 description 5
LIOPHZNMBKHGAV-UHFFFAOYSA-M potassium;2-(phosphonomethylamino)acetate Chemical class [K+].OC(=O)CNCP(O)([O-])=O LIOPHZNMBKHGAV-UHFFFAOYSA-M 0.000 description 5
239000000126 substance Substances 0.000 description 5
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 description 4
HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 4
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 description 4
QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 4
239000003905 agrochemical Substances 0.000 description 4
150000001412 amines Chemical class 0.000 description 4
239000008346 aqueous phase Substances 0.000 description 4
230000015572 biosynthetic process Effects 0.000 description 4
150000001875 compounds Chemical class 0.000 description 4
IWEDIXLBFLAXBO-UHFFFAOYSA-N dicamba Chemical compound COC1=C(Cl)C=CC(Cl)=C1C(O)=O IWEDIXLBFLAXBO-UHFFFAOYSA-N 0.000 description 4
229920001903 high density polyethylene Polymers 0.000 description 4
239000004700 high-density polyethylene Substances 0.000 description 4
150000002431 hydrogen Chemical class 0.000 description 4
230000006872 improvement Effects 0.000 description 4
NQQVFXUMIDALNH-UHFFFAOYSA-N picloram Chemical compound NC1=C(Cl)C(Cl)=NC(C(O)=O)=C1Cl NQQVFXUMIDALNH-UHFFFAOYSA-N 0.000 description 4
150000003568 thioethers Chemical class 0.000 description 4
239000002794 2,4-DB Substances 0.000 description 3
YIVXMZJTEQBPQO-UHFFFAOYSA-N 2,4-DB Chemical compound OC(=O)CCCOC1=CC=C(Cl)C=C1Cl YIVXMZJTEQBPQO-UHFFFAOYSA-N 0.000 description 3
239000005504 Dicamba Substances 0.000 description 3
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
WHKUVVPPKQRRBV-UHFFFAOYSA-N Trasan Chemical compound CC1=CC(Cl)=CC=C1OCC(O)=O WHKUVVPPKQRRBV-UHFFFAOYSA-N 0.000 description 3
238000013459 approach Methods 0.000 description 3
238000013461 design Methods 0.000 description 3
238000009826 distribution Methods 0.000 description 3
150000002148 esters Chemical class 0.000 description 3
150000002338 glycosides Chemical class 0.000 description 3
239000000463 material Substances 0.000 description 3
125000004430 oxygen atom Chemical group O* 0.000 description 3
238000004806 packaging method and process Methods 0.000 description 3
150000007970 thio esters Chemical class 0.000 description 3
239000005631 2,4-Dichlorophenoxyacetic acid Substances 0.000 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 description 2
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 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 description 2
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 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 description 2
LLWADFLAOKUBDR-UHFFFAOYSA-N 2-methyl-4-chlorophenoxybutyric acid Chemical compound CC1=CC(Cl)=CC=C1OCCCC(O)=O LLWADFLAOKUBDR-UHFFFAOYSA-N 0.000 description 2
239000005500 Clopyralid Substances 0.000 description 2
239000005561 Glufosinate Substances 0.000 description 2
239000005566 Imazamox Substances 0.000 description 2
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 description 2
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
239000005574 MCPA Substances 0.000 description 2
239000005575 MCPB Substances 0.000 description 2
101150039283 MCPB gene Proteins 0.000 description 2
239000005595 Picloram Substances 0.000 description 2
239000005627 Triclopyr Substances 0.000 description 2
238000012271 agricultural production Methods 0.000 description 2
150000001408 amides Chemical class 0.000 description 2
150000003863 ammonium salts Chemical class 0.000 description 2
BFNBIHQBYMNNAN-UHFFFAOYSA-N ammonium sulfate Chemical compound N.N.OS(O)(=O)=O BFNBIHQBYMNNAN-UHFFFAOYSA-N 0.000 description 2
229910052921 ammonium sulfate Inorganic materials 0.000 description 2
235000011130 ammonium sulphate Nutrition 0.000 description 2
229910052799 carbon Inorganic materials 0.000 description 2
239000003795 chemical substances by application Substances 0.000 description 2
QZXCCPZJCKEPSA-UHFFFAOYSA-N chlorfenac Chemical compound OC(=O)CC1=C(Cl)C=CC(Cl)=C1Cl QZXCCPZJCKEPSA-UHFFFAOYSA-N 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
238000010586 diagram Methods 0.000 description 2
230000007613 environmental effect Effects 0.000 description 2
239000011521 glass Substances 0.000 description 2
150000008131 glucosides Chemical group 0.000 description 2
150000002334 glycols Chemical class 0.000 description 2
WXUNXXKSYBUHMK-UHFFFAOYSA-N methyl 4-methyl-2-(4-methyl-5-oxo-4-propan-2-yl-1h-imidazol-2-yl)benzoate;methyl 5-methyl-2-(4-methyl-5-oxo-4-propan-2-yl-1h-imidazol-2-yl)benzoate Chemical compound COC(=O)C1=CC=C(C)C=C1C1=NC(C)(C(C)C)C(=O)N1.COC(=O)C1=CC(C)=CC=C1C1=NC(C)(C(C)C)C(=O)N1 WXUNXXKSYBUHMK-UHFFFAOYSA-N 0.000 description 2
FBUKVWPVBMHYJY-UHFFFAOYSA-N nonanoic acid Chemical compound CCCCCCCCC(O)=O FBUKVWPVBMHYJY-UHFFFAOYSA-N 0.000 description 2
230000034958 pharyngeal pumping Effects 0.000 description 2
239000012071 phase Substances 0.000 description 2
229920001451 polypropylene glycol Polymers 0.000 description 2
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230000009467 reduction Effects 0.000 description 2
238000005507 spraying Methods 0.000 description 2
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150000003462 sulfoxides Chemical class 0.000 description 2
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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
XZIDTOHMJBOSOX-UHFFFAOYSA-N 2,3,6-TBA Chemical compound OC(=O)C1=C(Cl)C=CC(Cl)=C1Cl XZIDTOHMJBOSOX-UHFFFAOYSA-N 0.000 description 1
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BCOVXKWQTYUMNW-UHFFFAOYSA-N 2-(2,4-dichlorophenoxy)butanoic acid Chemical compound CCC(C(O)=O)OC1=CC=C(Cl)C=C1Cl BCOVXKWQTYUMNW-UHFFFAOYSA-N 0.000 description 1
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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 description 1
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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 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
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
CAAMSDWKXXPUJR-UHFFFAOYSA-N 3,5-dihydro-4H-imidazol-4-one Chemical compound O=C1CNC=N1 CAAMSDWKXXPUJR-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
NYRMIJKDBAQCHC-UHFFFAOYSA-N 5-(methylamino)-2-phenyl-4-[3-(trifluoromethyl)phenyl]furan-3(2H)-one Chemical compound O1C(NC)=C(C=2C=C(C=CC=2)C(F)(F)F)C(=O)C1C1=CC=CC=C1 NYRMIJKDBAQCHC-UHFFFAOYSA-N 0.000 description 1
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 description 1
DVOODWOZJVJKQR-UHFFFAOYSA-N 5-tert-butyl-3-(2,4-dichloro-5-prop-2-ynoxyphenyl)-1,3,4-oxadiazol-2-one Chemical group O=C1OC(C(C)(C)C)=NN1C1=CC(OCC#C)=C(Cl)C=C1Cl DVOODWOZJVJKQR-UHFFFAOYSA-N 0.000 description 1
VTNQPKFIQCLBDU-UHFFFAOYSA-N Acetochlor Chemical compound CCOCN(C(=O)CCl)C1=C(C)C=CC=C1CC VTNQPKFIQCLBDU-UHFFFAOYSA-N 0.000 description 1
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NXQDBZGWYSEGFL-UHFFFAOYSA-N Anilofos Chemical compound COP(=S)(OC)SCC(=O)N(C(C)C)C1=CC=C(Cl)C=C1 NXQDBZGWYSEGFL-UHFFFAOYSA-N 0.000 description 1
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239000005471 Benfluralin Substances 0.000 description 1
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239000005476 Bentazone Substances 0.000 description 1
239000005488 Bispyribac Substances 0.000 description 1
239000004135 Bone phosphate Substances 0.000 description 1
CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 1
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239000005489 Bromoxynil Substances 0.000 description 1
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239000005490 Carbetamide Substances 0.000 description 1
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NLYNUTMZTCLNOO-UHFFFAOYSA-N Chlorbromuron Chemical compound CON(C)C(=O)NC1=CC=C(Br)C(Cl)=C1 NLYNUTMZTCLNOO-UHFFFAOYSA-N 0.000 description 1
239000005493 Chloridazon (aka pyrazone) Substances 0.000 description 1
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
239000005494 Chlorotoluron Substances 0.000 description 1
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VHCNQEUWZYOAEV-UHFFFAOYSA-N metamitron Chemical compound O=C1N(N)C(C)=NN=C1C1=CC=CC=C1 VHCNQEUWZYOAEV-UHFFFAOYSA-N 0.000 description 1
STEPQTYSZVCJPV-UHFFFAOYSA-N metazachlor Chemical compound CC1=CC=CC(C)=C1N(C(=O)CCl)CN1N=CC=C1 STEPQTYSZVCJPV-UHFFFAOYSA-N 0.000 description 1
MFSWTRQUCLNFOM-UHFFFAOYSA-N methyl 2-(4-{[3-chloro-5-(trifluoromethyl)pyridin-2-yl]oxy}phenoxy)propanoate Chemical group C1=CC(OC(C)C(=O)OC)=CC=C1OC1=NC=C(C(F)(F)F)C=C1Cl MFSWTRQUCLNFOM-UHFFFAOYSA-N 0.000 description 1
RBNIGDFIUWJJEV-UHFFFAOYSA-N methyl 2-(n-benzoyl-3-chloro-4-fluoroanilino)propanoate Chemical group C=1C=C(F)C(Cl)=CC=1N(C(C)C(=O)OC)C(=O)C1=CC=CC=C1 RBNIGDFIUWJJEV-UHFFFAOYSA-N 0.000 description 1
BACHBFVBHLGWSL-UHFFFAOYSA-N methyl 2-[4-(2,4-dichlorophenoxy)phenoxy]propanoate Chemical group C1=CC(OC(C)C(=O)OC)=CC=C1OC1=CC=C(Cl)C=C1Cl BACHBFVBHLGWSL-UHFFFAOYSA-N 0.000 description 1
NDNKHWUXXOFHTD-UHFFFAOYSA-N metizoline Chemical compound CC=1SC2=CC=CC=C2C=1CC1=NCCN1 NDNKHWUXXOFHTD-UHFFFAOYSA-N 0.000 description 1
229960002939 metizoline Drugs 0.000 description 1
DSRNRYQBBJQVCW-UHFFFAOYSA-N metoxuron Chemical compound COC1=CC=C(NC(=O)N(C)C)C=C1Cl DSRNRYQBBJQVCW-UHFFFAOYSA-N 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
239000004530 micro-emulsion Substances 0.000 description 1
239000003595 mist Substances 0.000 description 1
238000012986 modification Methods 0.000 description 1
230000004048 modification Effects 0.000 description 1
DEDOPGXGGQYYMW-UHFFFAOYSA-N molinate Chemical compound CCSC(=O)N1CCCCCC1 DEDOPGXGGQYYMW-UHFFFAOYSA-N 0.000 description 1
238000012544 monitoring process Methods 0.000 description 1
YWFWDNVOPHGWMX-UHFFFAOYSA-N n,n-dimethyldodecan-1-amine Chemical compound CCCCCCCCCCCCN(C)C YWFWDNVOPHGWMX-UHFFFAOYSA-N 0.000 description 1
SKSVCKGZZUFGGC-UHFFFAOYSA-N n-methylmethanamine;propanoic acid Chemical compound C[NH2+]C.CCC([O-])=O SKSVCKGZZUFGGC-UHFFFAOYSA-N 0.000 description 1
NNKSAZWMTWKXLD-UHFFFAOYSA-N n-methyloctadecan-1-amine;hydrochloride Chemical compound [Cl-].CCCCCCCCCCCCCCCCCC[NH2+]C NNKSAZWMTWKXLD-UHFFFAOYSA-N 0.000 description 1
239000003921 oil Substances 0.000 description 1
JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
IOXAXYHXMLCCJJ-UHFFFAOYSA-N oxetan-3-yl 2-[(4,6-dimethylpyrimidin-2-yl)carbamoylsulfamoyl]benzoate Chemical compound CC1=CC(C)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2)C(=O)OC2COC2)=N1 IOXAXYHXMLCCJJ-UHFFFAOYSA-N 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
230000000361 pesticidal effect Effects 0.000 description 1
IDOWTHOLJBTAFI-UHFFFAOYSA-N phenmedipham Chemical compound COC(=O)NC1=CC=CC(OC(=O)NC=2C=C(C)C=CC=2)=C1 IDOWTHOLJBTAFI-UHFFFAOYSA-N 0.000 description 1
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 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
239000004033 plastic Substances 0.000 description 1
229920003023 plastic Polymers 0.000 description 1
229920000570 polyether Polymers 0.000 description 1
229920001223 polyethylene glycol Polymers 0.000 description 1
159000000001 potassium salts Chemical class 0.000 description 1
239000000843 powder 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
ISEUFVQQFVOBCY-UHFFFAOYSA-N prometon Chemical compound COC1=NC(NC(C)C)=NC(NC(C)C)=N1 ISEUFVQQFVOBCY-UHFFFAOYSA-N 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
MFOUDYKPLGXPGO-UHFFFAOYSA-N propachlor Chemical compound ClCC(=O)N(C(C)C)C1=CC=CC=C1 MFOUDYKPLGXPGO-UHFFFAOYSA-N 0.000 description 1
ASRAWSBMDXVNLX-UHFFFAOYSA-N pyrazolynate Chemical compound C=1C=C(Cl)C=C(Cl)C=1C(=O)C=1C(C)=NN(C)C=1OS(=O)(=O)C1=CC=C(C)C=C1 ASRAWSBMDXVNLX-UHFFFAOYSA-N 0.000 description 1
VTRWMTJQBQJKQH-UHFFFAOYSA-N pyributicarb Chemical compound COC1=CC=CC(N(C)C(=S)OC=2C=C(C=CC=2)C(C)(C)C)=N1 VTRWMTJQBQJKQH-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
150000003242 quaternary ammonium salts Chemical class 0.000 description 1
FFSSWMQPCJRCRV-UHFFFAOYSA-N quinclorac Chemical compound ClC1=CN=C2C(C(=O)O)=C(Cl)C=CC2=C1 FFSSWMQPCJRCRV-UHFFFAOYSA-N 0.000 description 1
ALZOLUNSQWINIR-UHFFFAOYSA-N quinmerac Chemical compound OC(=O)C1=C(Cl)C=CC2=CC(C)=CN=C21 ALZOLUNSQWINIR-UHFFFAOYSA-N 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
239000011541 reaction mixture Substances 0.000 description 1
238000004064 recycling Methods 0.000 description 1
239000012088 reference solution Substances 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
231100000323 severe irritant Toxicity 0.000 description 1
ODCWYMIRDDJXKW-UHFFFAOYSA-N simazine Chemical compound CCNC1=NC(Cl)=NC(NCC)=N1 ODCWYMIRDDJXKW-UHFFFAOYSA-N 0.000 description 1
MGLWZSOBALDPEK-UHFFFAOYSA-N simetryn Chemical compound CCNC1=NC(NCC)=NC(SC)=N1 MGLWZSOBALDPEK-UHFFFAOYSA-N 0.000 description 1
159000000000 sodium salts Chemical class 0.000 description 1
239000002689 soil Substances 0.000 description 1
239000002904 solvent Substances 0.000 description 1
239000007921 spray Substances 0.000 description 1
239000007858 starting material Substances 0.000 description 1
239000010959 steel Substances 0.000 description 1
238000003756 stirring Methods 0.000 description 1
238000006467 substitution reaction 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
239000000725 suspension Substances 0.000 description 1
229940095064 tartrate Drugs 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
238000012360 testing method Methods 0.000 description 1
239000002562 thickening agent Substances 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
DQFPEYARZIQXRM-LTGZKZEYSA-N tralkoxydim Chemical compound C1C(=O)C(C(/CC)=N/OCC)=C(O)CC1C1=C(C)C=C(C)C=C1C DQFPEYARZIQXRM-LTGZKZEYSA-N 0.000 description 1
238000012546 transfer Methods 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
BQZXUHDXIARLEO-UHFFFAOYSA-N tribenuron Chemical compound COC1=NC(C)=NC(N(C)C(=O)NS(=O)(=O)C=2C(=CC=CC=2)C(O)=O)=N1 BQZXUHDXIARLEO-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
230000000007 visual effect Effects 0.000 description 1
239000002699 waste material Substances 0.000 description 1
239000002023 wood 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
- 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
- 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
- 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

Landscapes

Life Sciences & Earth Sciences (AREA)
Health & Medical Sciences (AREA)
General Health & Medical Sciences (AREA)
Dentistry (AREA)
Plant Pathology (AREA)
Engineering & Computer Science (AREA)
Pest Control & Pesticides (AREA)
Agronomy & Crop Science (AREA)
Wood Science & Technology (AREA)
Zoology (AREA)
Environmental Sciences (AREA)
Toxicology (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)

SK708-2001A 1998-11-23 1999-11-19 Compact storage and shipping system for glyphosate herbicide SK7082001A3 (en)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
US10951498P	1998-11-23	1998-11-23
PCT/US1999/027479 WO2000030451A1 (fr)	1998-11-23	1999-11-19	Systeme compact de stockage et d'expedition pour herbicide glyphosate

Publications (1)

Publication Number	Publication Date
SK7082001A3 true SK7082001A3 (en)	2002-05-09

Family

ID=22328088

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
SK708-2001A SK7082001A3 (en)	1998-11-23	1999-11-19	Compact storage and shipping system for glyphosate herbicide

Country Status (25)

Country	Link
US (1)	US6544930B2 (fr)
EP (1)	EP1133232A1 (fr)
JP (2)	JP2002530304A (fr)
KR (1)	KR20010104305A (fr)
CN (1)	CN1277474C (fr)
AR (1)	AR018210A1 (fr)
AU (1)	AU775874B2 (fr)
BR (1)	BR9915966A (fr)
CA (1)	CA2351437C (fr)
CO (1)	CO5210916A1 (fr)
CZ (1)	CZ305415B6 (fr)
DK (1)	DK1438896T3 (fr)
EA (1)	EA200100574A1 (fr)
ES (1)	ES2552540T3 (fr)
GT (1)	GT199900200A (fr)
HU (1)	HU230853B1 (fr)
IL (1)	IL143273A0 (fr)
MY (1)	MY128777A (fr)
NO (1)	NO20012503L (fr)
NZ (1)	NZ511853A (fr)
PL (1)	PL231571B1 (fr)
SK (1)	SK7082001A3 (fr)
TR (2)	TR200200611T2 (fr)
UA (1)	UA75571C2 (fr)
WO (1)	WO2000030451A1 (fr)

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GB9819693D0 (en)	1998-09-10	1998-11-04	Zeneca Ltd	Glyphosate formulation
BR9915966A (pt) *	1998-11-23	2001-10-16	Monsanto Co	Armazenamento compacto e sistema de remessa para herbicida glifos+ato
ATE242601T1 (de) *	1998-12-23	2003-06-15	Huntsman Int Llc	Herbizide zusammensetzungen und tensidkonzentrate
MY158895A (en) *	2000-05-19	2016-11-30	Monsanto Technology Llc	Potassium glyphosate formulations
EP1333721B1 (fr) *	2000-10-17	2006-04-26	Victorian Chemical International Pty. Ltd.	Composition herbicide
AUPR682201A0 (en) *	2001-08-03	2001-08-30	Nufarm Limited	Glyphosate composition
AU2002358264A1 (en)	2001-12-21	2003-07-30	Dow Agrosciences Llc	High-strength low-viscosity agricultural formulations
WO2004093546A1 (fr) *	2003-04-22	2004-11-04	Monsanto Technology Llc	Compositions herbicides contenant du glyphosate et un analogue de pyridine
PL1722634T3 (pl)	2004-03-10	2011-12-30	Monsanto Technology Llc	Kompozycje herbicydowe zawierające N-fosfonometyloglicynę i herbicyd auksynowy
US8410022B2 (en)	2004-08-19	2013-04-02	Monsanto Technology Llc	Glyphosate salt herbicidal composition
WO2007109791A2 (fr) *	2006-03-23	2007-09-27	Akzo Nobel N.V.	Alkyle ether amines/alkylamines alcoxyles avec repartition en crete
BRPI0515898A (pt) *	2004-09-23	2008-08-12	Monsanto Technology Llc	processos para preparar alquil eter aminas/alquilaminas alcoxiladas com distribuição máxima, suas composições, tensoativos e formulações herbicidas estáveis
WO2006041702A2 (fr) *	2004-10-04	2006-04-20	Huntsman Petrochemical Corporation	Preparations de glyphosate de concentration elevee
US7419437B2 (en) *	2005-01-26	2008-09-02	Playstar, Inc.	Swing and swing packaging arrangement
CA2608206C (fr)	2005-05-24	2015-11-24	Monsanto Technology Llc	Amelioration de la compatibilite d'un herbicide
USD550325S1 (en)	2005-08-25	2007-09-04	Redball, Llc	Bulk container and support
US20070045355A1 (en) *	2005-08-25	2007-03-01	Claussen Steven W	Bulk container with collapsible support
US20100009937A1 (en) *	2006-09-22	2010-01-14	Huntsman Petrochemical Corporation	Pesticide formulation with streaming birefringence
US8133848B2 (en)	2007-09-04	2012-03-13	Nufarm Americas Inc.	Glyphosate composition and method of controlling weeds
AU2007216730B1 (en) *	2007-09-11	2009-01-15	Nufarm Americas Inc.	Glyphosate composition and method of controlling weeds
RU2479205C2 (ru) *	2007-12-13	2013-04-20	Донагис Индастриз Лимитед	Гербицидный состав триэтаноламиновой соли глифосата и способы подавления роста растений с его использованием
WO2009075591A1 (fr) *	2007-12-13	2009-06-18	Donaghys Industries Limited	Formulations herbicides pour des combinaisons de sels de diméthylamine et de potassium de glyphosate
AU2009296340B2 (en)	2008-09-29	2015-02-12	Monsanto Technology Llc	Glyphosate formulations containing amidoalkylamine surfactants
AU2009329535B2 (en) *	2008-12-19	2015-08-13	Basf Se	Aqueous flowable concentrate compositions of a microencapsulated dinitroaniline herbicide
US20120142532A1 (en)	2009-08-10	2012-06-07	Monsanto Technology Llc	Low volatility auxin herbicide formulations
AU2010317610B2 (en)	2009-11-16	2015-05-14	Imtrade Australia Pty Ltd	High load glyphosate formulations
CA2703354C (fr) *	2010-05-07	2012-10-02	Dennis Bulani	Manutention en vrac de produits chimiques pour l'agriculture et conteneur pour produits chimiques
BR112013007819B1 (pt)	2010-10-01	2018-05-08	Nufarm Australia Ltd	método de preparação de uma mistura aquosa de sais de glifosato para melhorar a manipulação da mistura
AU2012328638B2 (en)	2011-10-26	2016-11-17	Monsanto Technology Llc	Salts of carboxylic acid herbicides
UY34845A (es)	2012-06-04	2014-01-31	Monsanto Technology Llc	?composiciones herbicidas concentradas acuosas que contienen sales de glifosato y sales de dicamba
CA3123572A1 (fr)	2013-02-27	2014-09-04	Monsanto Technology Llc	Composition de glyphosate pour melanges en cuve de dicamba avec une volatilite amelioree
USD765816S1 (en)	2015-05-27	2016-09-06	Claussen Technology, Llc	Transfer system platform
EP3454658B1 (fr)	2016-05-11	2024-11-27	Monsanto Technology LLC	Formulations de glyphosate contenant des tensioactifs d'amidoalkylamine
US11109591B2 (en)	2017-04-24	2021-09-07	Taminco Bvba	Single phase liquids of alkanolamine salts of dicamba
BR102018004761B1 (pt)	2018-03-09	2023-03-07	Ouro Fino Química S.A.	Composição herbicia de glifosato de alta carga, formulação pronta para uso obtida a partir da composição e método para controlar várias espécies de plantas daninhas em culturas agrícolas

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US3799758A (en) *	1971-08-09	1974-03-26	Monsanto Co	N-phosphonomethyl-glycine phytotoxicant compositions
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GB9002495D0 (en)	1990-02-05	1990-04-04	Monsanto Europe Sa	Glyphosate compositions
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GB9819693D0 (en) *	1998-09-10	1998-11-04	Zeneca Ltd	Glyphosate formulation
BR9915966A (pt) *	1998-11-23	2001-10-16	Monsanto Co	Armazenamento compacto e sistema de remessa para herbicida glifos+ato

1999
- 1999-11-19 BR BR9915966-0A patent/BR9915966A/pt not_active Application Discontinuation
- 1999-11-19 EA EA200100574A patent/EA200100574A1/ru unknown
- 1999-11-19 CA CA2351437A patent/CA2351437C/fr not_active Expired - Lifetime
- 1999-11-19 KR KR1020017006480A patent/KR20010104305A/ko not_active Withdrawn
- 1999-11-19 PL PL348678A patent/PL231571B1/pl unknown
- 1999-11-19 ES ES04008937.7T patent/ES2552540T3/es not_active Expired - Lifetime
- 1999-11-19 AU AU18241/00A patent/AU775874B2/en not_active Expired
- 1999-11-19 JP JP2000583349A patent/JP2002530304A/ja active Pending
- 1999-11-19 UA UA2001064394A patent/UA75571C2/uk unknown
- 1999-11-19 NZ NZ511853A patent/NZ511853A/en not_active IP Right Cessation
- 1999-11-19 IL IL14327399A patent/IL143273A0/xx unknown
- 1999-11-19 HU HU0104585A patent/HU230853B1/hu unknown
- 1999-11-19 SK SK708-2001A patent/SK7082001A3/sk unknown
- 1999-11-19 CZ CZ2001-1791A patent/CZ305415B6/cs not_active IP Right Cessation
- 1999-11-19 EP EP99961722A patent/EP1133232A1/fr not_active Withdrawn
- 1999-11-19 TR TR2002/00611T patent/TR200200611T2/xx unknown
- 1999-11-19 WO PCT/US1999/027479 patent/WO2000030451A1/fr not_active Ceased
- 1999-11-19 DK DK04008937.7T patent/DK1438896T3/en active
- 1999-11-19 TR TR2001/01523T patent/TR200101523T2/xx unknown
- 1999-11-19 CN CNB998152730A patent/CN1277474C/zh not_active Expired - Lifetime
- 1999-11-22 AR ARP990105947A patent/AR018210A1/es active IP Right Grant
- 1999-11-22 MY MYPI99005090A patent/MY128777A/en unknown
- 1999-11-23 CO CO99073755A patent/CO5210916A1/es not_active Application Discontinuation
- 1999-11-25 GT GT199900200A patent/GT199900200A/es unknown
2001
- 2001-05-22 NO NO20012503A patent/NO20012503L/no not_active Application Discontinuation
- 2001-11-16 US US09/992,728 patent/US6544930B2/en not_active Expired - Lifetime
2012
- 2012-01-05 JP JP2012000800A patent/JP2012062334A/ja active Pending

Also Published As

Publication number	Publication date
NO20012503D0 (no)	2001-05-22
EP1133232A1 (fr)	2001-09-19
IL143273A0 (en)	2002-04-21
CA2351437C (fr)	2011-05-24
CN1277474C (zh)	2006-10-04
BR9915966A (pt)	2001-10-16
JP2002530304A (ja)	2002-09-17
TR200200611T2 (tr)	2002-06-21
WO2000030451A1 (fr)	2000-06-02
CN1332606A (zh)	2002-01-23
NZ511853A (en)	2003-12-19
HUP0104585A2 (en)	2002-05-29
AR018210A1 (es)	2001-10-31
CA2351437A1 (fr)	2000-06-02
US20020065199A1 (en)	2002-05-30
CZ305415B6 (cs)	2015-09-09
ES2552540T3 (es)	2015-11-30
MY128777A (en)	2007-02-28
AU1824100A (en)	2000-06-13
EA200100574A1 (ru)	2001-12-24
PL231571B1 (pl)	2019-03-29
PL348678A1 (en)	2002-06-03
UA75571C2 (uk)	2006-05-15
US6544930B2 (en)	2003-04-08
NO20012503L (no)	2001-07-11
JP2012062334A (ja)	2012-03-29
CO5210916A1 (es)	2002-10-30
DK1438896T3 (en)	2015-11-16
KR20010104305A (ko)	2001-11-24
AU775874B2 (en)	2004-08-19
TR200101523T2 (tr)	2001-10-22
HU230853B1 (en)	2018-09-28
GT199900200A (es)	2001-05-18
CZ20011791A3 (cs)	2001-11-14

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