JP2009531169A5 - - Google Patents
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- JP2009531169A5 JP2009531169A5 JP2009501956A JP2009501956A JP2009531169A5 JP 2009531169 A5 JP2009531169 A5 JP 2009531169A5 JP 2009501956 A JP2009501956 A JP 2009501956A JP 2009501956 A JP2009501956 A JP 2009501956A JP 2009531169 A5 JP2009531169 A5 JP 2009531169A5
- Authority
- JP
- Japan
- Prior art keywords
- microcapsule
- compound
- microcapsules
- microencapsulated
- substance
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
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- 239000012948 isocyanate Substances 0.000 claims description 32
- 239000000203 mixture Substances 0.000 claims description 30
- -1 aliphatic isocyanates Chemical class 0.000 claims description 28
- 238000000034 method Methods 0.000 claims description 7
- UPMLOUAZCHDJJD-UHFFFAOYSA-N 4,4'-Diphenylmethane Diisocyanate Chemical group C1=CC(N=C=O)=CC=C1CC1=CC=C(N=C=O)C=C1 UPMLOUAZCHDJJD-UHFFFAOYSA-N 0.000 claims description 6
- 239000000539 dimer Substances 0.000 claims description 4
- 239000002253 acid Substances 0.000 claims description 3
- 239000003094 microcapsule Substances 0.000 claims 87
- 150000001875 compounds Chemical class 0.000 claims 49
- 239000000126 substance Substances 0.000 claims 24
- 238000009472 formulation Methods 0.000 claims 13
- 239000000463 material Substances 0.000 claims 12
- 239000000178 monomer Substances 0.000 claims 11
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims 9
- 239000004094 surface-active agent Substances 0.000 claims 8
- 239000012071 phase Substances 0.000 claims 7
- 239000004480 active ingredient Substances 0.000 claims 6
- 229910052739 hydrogen Inorganic materials 0.000 claims 6
- 239000001257 hydrogen Substances 0.000 claims 6
- 238000004519 manufacturing process Methods 0.000 claims 6
- 125000001424 substituent group Chemical group 0.000 claims 6
- 229920000642 polymer Polymers 0.000 claims 5
- NLZUEZXRPGMBCV-UHFFFAOYSA-N Butylhydroxytoluene Chemical compound CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 NLZUEZXRPGMBCV-UHFFFAOYSA-N 0.000 claims 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 4
- 229920001400 block copolymer Polymers 0.000 claims 4
- CZBZUDVBLSSABA-UHFFFAOYSA-N butylated hydroxyanisole Chemical compound COC1=CC=C(O)C(C(C)(C)C)=C1.COC1=CC=C(O)C=C1C(C)(C)C CZBZUDVBLSSABA-UHFFFAOYSA-N 0.000 claims 4
- 239000004490 capsule suspension Substances 0.000 claims 4
- 239000003054 catalyst Substances 0.000 claims 4
- 238000006243 chemical reaction Methods 0.000 claims 4
- 239000003921 oil Substances 0.000 claims 4
- 239000007787 solid Substances 0.000 claims 4
- 239000004546 suspension concentrate Substances 0.000 claims 4
- 239000005499 Clomazone Substances 0.000 claims 3
- 239000004372 Polyvinyl alcohol Substances 0.000 claims 3
- 239000003905 agrochemical Substances 0.000 claims 3
- 239000003963 antioxidant agent Substances 0.000 claims 3
- 239000008346 aqueous phase Substances 0.000 claims 3
- 230000009286 beneficial effect Effects 0.000 claims 3
- 239000003795 chemical substances by application Substances 0.000 claims 3
- KIEDNEWSYUYDSN-UHFFFAOYSA-N clomazone Chemical compound O=C1C(C)(C)CON1CC1=CC=CC=C1Cl KIEDNEWSYUYDSN-UHFFFAOYSA-N 0.000 claims 3
- 235000014113 dietary fatty acids Nutrition 0.000 claims 3
- 239000000194 fatty acid Substances 0.000 claims 3
- 229930195729 fatty acid Natural products 0.000 claims 3
- 239000012782 phase change material Substances 0.000 claims 3
- 229920002451 polyvinyl alcohol Polymers 0.000 claims 3
- 239000000243 solution Substances 0.000 claims 3
- ZXQYGBMAQZUVMI-RDDWSQKMSA-N (1S)-cis-(alphaR)-cyhalothrin Chemical compound CC1(C)[C@H](\C=C(/Cl)C(F)(F)F)[C@@H]1C(=O)O[C@@H](C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 ZXQYGBMAQZUVMI-RDDWSQKMSA-N 0.000 claims 2
- PXMNMQRDXWABCY-UHFFFAOYSA-N 1-(4-chlorophenyl)-4,4-dimethyl-3-(1H-1,2,4-triazol-1-ylmethyl)pentan-3-ol Chemical group C1=NC=NN1CC(O)(C(C)(C)C)CCC1=CC=C(Cl)C=C1 PXMNMQRDXWABCY-UHFFFAOYSA-N 0.000 claims 2
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical group CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 claims 2
- ULQISTXYYBZJSJ-UHFFFAOYSA-N 12-hydroxyoctadecanoic acid Chemical compound CCCCCCC(O)CCCCCCCCCCC(O)=O ULQISTXYYBZJSJ-UHFFFAOYSA-N 0.000 claims 2
- 239000005535 Flurochloridone Substances 0.000 claims 2
- 238000012695 Interfacial polymerization Methods 0.000 claims 2
- VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical group CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 claims 2
- 229920001732 Lignosulfonate Polymers 0.000 claims 2
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 claims 2
- 239000005839 Tebuconazole Substances 0.000 claims 2
- 230000006750 UV protection Effects 0.000 claims 2
- XCSGPAVHZFQHGE-UHFFFAOYSA-N alachlor Chemical compound CCC1=CC=CC(CC)=C1N(COC)C(=O)CCl XCSGPAVHZFQHGE-UHFFFAOYSA-N 0.000 claims 2
- IYABWNGZIDDRAK-UHFFFAOYSA-N allene Chemical group C=C=C IYABWNGZIDDRAK-UHFFFAOYSA-N 0.000 claims 2
- 239000002775 capsule Substances 0.000 claims 2
- 239000000084 colloidal system Substances 0.000 claims 2
- 229920001577 copolymer Polymers 0.000 claims 2
- 239000006185 dispersion Substances 0.000 claims 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 2
- 150000004665 fatty acids Chemical class 0.000 claims 2
- OQZCSNDVOWYALR-UHFFFAOYSA-N flurochloridone Chemical group FC(F)(F)C1=CC=CC(N2C(C(Cl)C(CCl)C2)=O)=C1 OQZCSNDVOWYALR-UHFFFAOYSA-N 0.000 claims 2
- 229920000578 graft copolymer Polymers 0.000 claims 2
- 150000002431 hydrogen Chemical class 0.000 claims 2
- 125000004029 hydroxymethyl group Chemical group [H]OC([H])([H])* 0.000 claims 2
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 claims 2
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 2
- 239000005910 lambda-Cyhalothrin Substances 0.000 claims 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 2
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims 2
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 claims 2
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 claims 2
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 claims 2
- 239000011814 protection agent Substances 0.000 claims 2
- 230000001681 protective effect Effects 0.000 claims 2
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 2
- 239000002904 solvent Substances 0.000 claims 2
- 239000000725 suspension Substances 0.000 claims 2
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims 2
- 239000013638 trimer Substances 0.000 claims 2
- KAATUXNTWXVJKI-NSHGMRRFSA-N (1R)-cis-(alphaS)-cypermethrin Chemical group CC1(C)[C@@H](C=C(Cl)Cl)[C@H]1C(=O)O[C@H](C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 KAATUXNTWXVJKI-NSHGMRRFSA-N 0.000 claims 1
- SBNFWQZLDJGRLK-RTWAWAEBSA-N (1R)-trans-phenothrin Chemical compound CC1(C)[C@H](C=C(C)C)[C@H]1C(=O)OCC1=CC=CC(OC=2C=CC=CC=2)=C1 SBNFWQZLDJGRLK-RTWAWAEBSA-N 0.000 claims 1
- ZMYFCFLJBGAQRS-IRXDYDNUSA-N (2R,3S)-epoxiconazole Chemical compound C1=CC(F)=CC=C1[C@@]1(CN2N=CN=C2)[C@H](C=2C(=CC=CC=2)Cl)O1 ZMYFCFLJBGAQRS-IRXDYDNUSA-N 0.000 claims 1
- XMAYWYJOQHXEEK-OZXSUGGESA-N (2R,4S)-ketoconazole Chemical compound C1CN(C(=O)C)CCN1C(C=C1)=CC=C1OC[C@@H]1O[C@@](CN2C=NC=C2)(C=2C(=CC(Cl)=CC=2)Cl)OC1 XMAYWYJOQHXEEK-OZXSUGGESA-N 0.000 claims 1
- AZYRZNIYJDKRHO-UHFFFAOYSA-N 1,3-bis(2-isocyanatopropan-2-yl)benzene Chemical group O=C=NC(C)(C)C1=CC=CC(C(C)(C)N=C=O)=C1 AZYRZNIYJDKRHO-UHFFFAOYSA-N 0.000 claims 1
- 229940114072 12-hydroxystearic acid Drugs 0.000 claims 1
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 claims 1
- 239000005877 Alpha-Cypermethrin Substances 0.000 claims 1
- 239000005944 Chlorpyrifos Substances 0.000 claims 1
- 239000005767 Epoxiconazole Substances 0.000 claims 1
- 239000005558 Fluroxypyr Substances 0.000 claims 1
- 239000005580 Metazachlor Substances 0.000 claims 1
- 239000005591 Pendimethalin Substances 0.000 claims 1
- 239000004698 Polyethylene Substances 0.000 claims 1
- 239000005822 Propiconazole Substances 0.000 claims 1
- 239000004113 Sepiolite Substances 0.000 claims 1
- 235000021355 Stearic acid Nutrition 0.000 claims 1
- 241000607479 Yersinia pestis Species 0.000 claims 1
- 229910021536 Zeolite Inorganic materials 0.000 claims 1
- VXSIXFKKSNGRRO-MXOVTSAMSA-N [(1s)-2-methyl-4-oxo-3-[(2z)-penta-2,4-dienyl]cyclopent-2-en-1-yl] (1r,3r)-2,2-dimethyl-3-(2-methylprop-1-enyl)cyclopropane-1-carboxylate;[(1s)-2-methyl-4-oxo-3-[(2z)-penta-2,4-dienyl]cyclopent-2-en-1-yl] (1r,3r)-3-[(e)-3-methoxy-2-methyl-3-oxoprop-1-enyl Chemical class CC1(C)[C@H](C=C(C)C)[C@H]1C(=O)O[C@@H]1C(C)=C(C\C=C/C=C)C(=O)C1.CC1(C)[C@H](/C=C(\C)C(=O)OC)[C@H]1C(=O)O[C@@H]1C(C)=C(C\C=C/C=C)C(=O)C1 VXSIXFKKSNGRRO-MXOVTSAMSA-N 0.000 claims 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims 1
- 239000013543 active substance Substances 0.000 claims 1
- 150000001298 alcohols Chemical class 0.000 claims 1
- 239000003242 anti bacterial agent Substances 0.000 claims 1
- 239000000729 antidote Substances 0.000 claims 1
- 230000003078 antioxidant effect Effects 0.000 claims 1
- 239000012736 aqueous medium Substances 0.000 claims 1
- 239000007864 aqueous solution Substances 0.000 claims 1
- 239000007900 aqueous suspension Substances 0.000 claims 1
- VEMKTZHHVJILDY-UXHICEINSA-N bioresmethrin Chemical compound CC1(C)[C@H](C=C(C)C)[C@H]1C(=O)OCC1=COC(CC=2C=CC=CC=2)=C1 VEMKTZHHVJILDY-UXHICEINSA-N 0.000 claims 1
- 230000000903 blocking effect Effects 0.000 claims 1
- SBPBAQFWLVIOKP-UHFFFAOYSA-N chlorpyrifos Chemical group CCOP(=S)(OCC)OC1=NC(Cl)=C(Cl)C=C1Cl SBPBAQFWLVIOKP-UHFFFAOYSA-N 0.000 claims 1
- 239000004927 clay Substances 0.000 claims 1
- 238000000576 coating method Methods 0.000 claims 1
- 238000010790 dilution Methods 0.000 claims 1
- 239000012895 dilution Substances 0.000 claims 1
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 claims 1
- 239000002270 dispersing agent Substances 0.000 claims 1
- RDYMFSUJUZBWLH-SVWSLYAFSA-N endosulfan Chemical group C([C@@H]12)OS(=O)OC[C@@H]1[C@]1(Cl)C(Cl)=C(Cl)[C@@]2(Cl)C1(Cl)Cl RDYMFSUJUZBWLH-SVWSLYAFSA-N 0.000 claims 1
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 claims 1
- 239000004744 fabric Substances 0.000 claims 1
- 238000001914 filtration Methods 0.000 claims 1
- 239000013020 final formulation Substances 0.000 claims 1
- MEFQWPUMEMWTJP-UHFFFAOYSA-N fluroxypyr Chemical group NC1=C(Cl)C(F)=NC(OCC(O)=O)=C1Cl MEFQWPUMEMWTJP-UHFFFAOYSA-N 0.000 claims 1
- 230000000855 fungicidal effect Effects 0.000 claims 1
- 239000000417 fungicide Substances 0.000 claims 1
- 150000002334 glycols Chemical class 0.000 claims 1
- VPVSTMAPERLKKM-UHFFFAOYSA-N glycoluril Chemical class N1C(=O)NC2NC(=O)NC21 VPVSTMAPERLKKM-UHFFFAOYSA-N 0.000 claims 1
- 238000000227 grinding Methods 0.000 claims 1
- 238000010438 heat treatment Methods 0.000 claims 1
- 239000000416 hydrocolloid Substances 0.000 claims 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 1
- 238000010348 incorporation Methods 0.000 claims 1
- 229960004125 ketoconazole Drugs 0.000 claims 1
- 238000002844 melting Methods 0.000 claims 1
- 230000008018 melting Effects 0.000 claims 1
- 239000012528 membrane Substances 0.000 claims 1
- 239000013335 mesoporous material Substances 0.000 claims 1
- STEPQTYSZVCJPV-UHFFFAOYSA-N metazachlor Chemical compound CC1=CC=CC(C)=C1N(C(=O)CCl)CN1N=CC=C1 STEPQTYSZVCJPV-UHFFFAOYSA-N 0.000 claims 1
- 238000002156 mixing Methods 0.000 claims 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 claims 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 claims 1
- 229910000489 osmium tetroxide Inorganic materials 0.000 claims 1
- 239000012285 osmium tetroxide Substances 0.000 claims 1
- 229910003445 palladium oxide Inorganic materials 0.000 claims 1
- 239000002245 particle Substances 0.000 claims 1
- CHIFOSRWCNZCFN-UHFFFAOYSA-N pendimethalin Chemical group CCC(CC)NC1=C([N+]([O-])=O)C=C(C)C(C)=C1[N+]([O-])=O CHIFOSRWCNZCFN-UHFFFAOYSA-N 0.000 claims 1
- 230000000361 pesticidal effect Effects 0.000 claims 1
- 239000000575 pesticide Substances 0.000 claims 1
- 239000003090 pesticide formulation Substances 0.000 claims 1
- 229960003536 phenothrin Drugs 0.000 claims 1
- 229910003446 platinum oxide Inorganic materials 0.000 claims 1
- 229920001223 polyethylene glycol Polymers 0.000 claims 1
- 229920000151 polyglycol Polymers 0.000 claims 1
- 239000010695 polyglycol Substances 0.000 claims 1
- 229920001451 polypropylene glycol Polymers 0.000 claims 1
- 229920000036 polyvinylpyrrolidone Polymers 0.000 claims 1
- 239000001267 polyvinylpyrrolidone Substances 0.000 claims 1
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 claims 1
- 239000000843 powder Substances 0.000 claims 1
- 239000002244 precipitate Substances 0.000 claims 1
- 238000002360 preparation method Methods 0.000 claims 1
- STJLVHWMYQXCPB-UHFFFAOYSA-N propiconazole Chemical compound O1C(CCC)COC1(C=1C(=CC(Cl)=CC=1)Cl)CN1N=CN=C1 STJLVHWMYQXCPB-UHFFFAOYSA-N 0.000 claims 1
- 125000002572 propoxy group Chemical group [*]OC([H])([H])C(C([H])([H])[H])([H])[H] 0.000 claims 1
- HYJYGLGUBUDSLJ-UHFFFAOYSA-N pyrethrin Natural products CCC(=O)OC1CC(=C)C2CC3OC3(C)C2C2OC(=O)C(=C)C12 HYJYGLGUBUDSLJ-UHFFFAOYSA-N 0.000 claims 1
- 229940070846 pyrethrins Drugs 0.000 claims 1
- 239000002728 pyrethroid Substances 0.000 claims 1
- 239000003620 semiochemical Substances 0.000 claims 1
- 229910052624 sepiolite Inorganic materials 0.000 claims 1
- 235000019355 sepiolite Nutrition 0.000 claims 1
- 239000008117 stearic acid Substances 0.000 claims 1
- 238000003756 stirring Methods 0.000 claims 1
- 239000004548 suspo-emulsion Substances 0.000 claims 1
- 229920001187 thermosetting polymer Polymers 0.000 claims 1
- 150000003852 triazoles Chemical class 0.000 claims 1
- ZSDSQXJSNMTJDA-UHFFFAOYSA-N trifluralin Chemical group CCCN(CCC)C1=C([N+]([O-])=O)C=C(C(F)(F)F)C=C1[N+]([O-])=O ZSDSQXJSNMTJDA-UHFFFAOYSA-N 0.000 claims 1
- 229920002554 vinyl polymer Polymers 0.000 claims 1
- 239000004034 viscosity adjusting agent Substances 0.000 claims 1
- 239000004563 wettable powder Substances 0.000 claims 1
- 239000000080 wetting agent Substances 0.000 claims 1
- 239000010457 zeolite Substances 0.000 claims 1
- 150000002513 isocyanates Chemical class 0.000 description 5
- 239000005056 polyisocyanate Substances 0.000 description 5
- 229920001228 polyisocyanate Polymers 0.000 description 5
- VZXPHDGHQXLXJC-UHFFFAOYSA-N 1,6-diisocyanato-5,6-dimethylheptane Chemical compound O=C=NC(C)(C)C(C)CCCCN=C=O VZXPHDGHQXLXJC-UHFFFAOYSA-N 0.000 description 4
- 239000005057 Hexamethylene diisocyanate Substances 0.000 description 4
- 125000005442 diisocyanate group Chemical group 0.000 description 4
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical compound C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 4
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 description 4
- NUKZAGXMHTUAFE-UHFFFAOYSA-N methyl hexanoate Chemical compound CCCCCC(=O)OC NUKZAGXMHTUAFE-UHFFFAOYSA-N 0.000 description 4
- 0 *C(C(*)(N1*)N2*)(N(*)C1=O)N(*)C2=O Chemical compound *C(C(*)(N1*)N2*)(N(*)C1=O)N(*)C2=O 0.000 description 2
- GFNDFCFPJQPVQL-UHFFFAOYSA-N 1,12-diisocyanatododecane Chemical compound O=C=NCCCCCCCCCCCCN=C=O GFNDFCFPJQPVQL-UHFFFAOYSA-N 0.000 description 2
- ZTNJGMFHJYGMDR-UHFFFAOYSA-N 1,2-diisocyanatoethane Chemical compound O=C=NCCN=C=O ZTNJGMFHJYGMDR-UHFFFAOYSA-N 0.000 description 2
- OHLKMGYGBHFODF-UHFFFAOYSA-N 1,4-bis(isocyanatomethyl)benzene Chemical compound O=C=NCC1=CC=C(CN=C=O)C=C1 OHLKMGYGBHFODF-UHFFFAOYSA-N 0.000 description 2
- OVBFMUAFNIIQAL-UHFFFAOYSA-N 1,4-diisocyanatobutane Chemical compound O=C=NCCCCN=C=O OVBFMUAFNIIQAL-UHFFFAOYSA-N 0.000 description 2
- ATOUXIOKEJWULN-UHFFFAOYSA-N 1,6-diisocyanato-2,2,4-trimethylhexane Chemical compound O=C=NCCC(C)CC(C)(C)CN=C=O ATOUXIOKEJWULN-UHFFFAOYSA-N 0.000 description 2
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 2
- 125000002723 alicyclic group Chemical group 0.000 description 2
- 125000001931 aliphatic group Chemical group 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- 235000010290 biphenyl Nutrition 0.000 description 2
- 239000004305 biphenyl Substances 0.000 description 2
- AYLRODJJLADBOB-QMMMGPOBSA-N methyl (2s)-2,6-diisocyanatohexanoate Chemical compound COC(=O)[C@@H](N=C=O)CCCCN=C=O AYLRODJJLADBOB-QMMMGPOBSA-N 0.000 description 2
- RTTZISZSHSCFRH-UHFFFAOYSA-N 1,3-bis(isocyanatomethyl)benzene Chemical compound O=C=NCC1=CC=CC(CN=C=O)=C1 RTTZISZSHSCFRH-UHFFFAOYSA-N 0.000 description 1
- ALQLPWJFHRMHIU-UHFFFAOYSA-N 1,4-diisocyanatobenzene Chemical compound O=C=NC1=CC=C(N=C=O)C=C1 ALQLPWJFHRMHIU-UHFFFAOYSA-N 0.000 description 1
- GNDOBZLRZOCGAS-UHFFFAOYSA-N 2-isocyanatoethyl 2,6-diisocyanatohexanoate Chemical compound O=C=NCCCCC(N=C=O)C(=O)OCCN=C=O GNDOBZLRZOCGAS-UHFFFAOYSA-N 0.000 description 1
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 1
- KIWIMEWVSKYONG-UHFFFAOYSA-N OC1CC(CCN=C=O)=C(CCN=C=O)CC1 Chemical compound OC1CC(CCN=C=O)=C(CCN=C=O)CC1 KIWIMEWVSKYONG-UHFFFAOYSA-N 0.000 description 1
- KXBFLNPZHXDQLV-UHFFFAOYSA-N [cyclohexyl(diisocyanato)methyl]cyclohexane Chemical compound C1CCCCC1C(N=C=O)(N=C=O)C1CCCCC1 KXBFLNPZHXDQLV-UHFFFAOYSA-N 0.000 description 1
- VBIAXKVXACZQFW-OWOJBTEDSA-N bis(2-isocyanatoethyl) (e)-but-2-enedioate Chemical compound O=C=NCCOC(=O)\C=C\C(=O)OCCN=C=O VBIAXKVXACZQFW-OWOJBTEDSA-N 0.000 description 1
- CZZYITDELCSZES-UHFFFAOYSA-N diphenylmethane Chemical compound C=1C=CC=CC=1CC1=CC=CC=C1 CZZYITDELCSZES-UHFFFAOYSA-N 0.000 description 1
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 1
- NIMLQBUJDJZYEJ-UHFFFAOYSA-N isophorone diisocyanate Chemical compound CC1(C)CC(N=C=O)CC(C)(CN=C=O)C1 NIMLQBUJDJZYEJ-UHFFFAOYSA-N 0.000 description 1
- DVKJHBMWWAPEIU-UHFFFAOYSA-N toluene 2,4-diisocyanate Chemical class CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 description 1
- RUELTTOHQODFPA-UHFFFAOYSA-N toluene 2,6-diisocyanate Chemical compound CC1=C(N=C=O)C=CC=C1N=C=O RUELTTOHQODFPA-UHFFFAOYSA-N 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP06006748.5 | 2006-03-30 | ||
| EP06006748.5A EP1840145B1 (en) | 2006-03-30 | 2006-03-30 | Acetylene carbamide derivatives-polyurea polymers and microcapsules and formulations thereof for controlled release |
| PCT/EP2007/002810 WO2007112934A1 (en) | 2006-03-30 | 2007-03-29 | Microcapsules with acetylene carbamide-polyurea polymers and formulations thereof for controlled release |
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Families Citing this family (69)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP1844653B1 (en) * | 2006-03-30 | 2017-07-26 | GAT Microencapsulation GmbH | Novel agrochemical formulations containing microcapsules |
| EP2628530A1 (de) * | 2008-03-11 | 2013-08-21 | Basf Se | Mikrokapseln mit Wänden aus Acylharnstoff |
| EP2225940B1 (en) | 2009-03-05 | 2014-03-12 | GAT Microencapsulation GmbH | Oil dispersions of nAChR binding neonicotinoids |
| EP2461689A1 (en) * | 2009-08-07 | 2012-06-13 | GAT Microencapsulation AG | Microcapsules containing macrolide lactones abamectin, milbemectin, avermectins, milbemycins, emamectins, ivermectins and mectins in general |
| AR079413A1 (es) * | 2009-10-07 | 2012-01-25 | Basf Se | Uso de particulas polimericas que comprenden insecticida para mejorar la movilidad en el suelo de insecticidas, formulaciones insecticidas, particulas polimericas que comprenden insecticida, y metodos para controlar plagas |
| CN101707994B (zh) * | 2009-12-09 | 2012-10-17 | 浙江森宇实业有限公司 | 一种针对铁皮石斛虫害的微胶囊靶向性农药制剂 |
| US10342230B2 (en) * | 2010-02-03 | 2019-07-09 | Upl Limited | ZC composition comprising microencapsulated pendimethalin |
| WO2012015467A1 (en) * | 2010-07-30 | 2012-02-02 | Dow Global Technologies Llc | Curable compositions |
| GB2483052B (en) | 2010-08-17 | 2012-12-19 | Rotam Agrochem Int Co Ltd | Herbicidal compositions |
| GB2483050B (en) * | 2010-08-17 | 2012-12-19 | Rotam Agrochem Int Co Ltd | Herbicidal compositions |
| CN103501604A (zh) * | 2010-09-17 | 2014-01-08 | 陶氏益农公司 | 稳定性提高的液体农业制剂 |
| CN102240531B (zh) * | 2011-03-21 | 2013-07-10 | 徐涵 | 一种植物细胞微球及其应用 |
| JP2012240925A (ja) * | 2011-05-16 | 2012-12-10 | Sumitomo Chemical Co Ltd | マイクロカプセル組成物の取得方法及びマイクロカプセル組成物 |
| AU2012365434B2 (en) * | 2011-11-02 | 2015-09-03 | Deepak Shah | Variable release water dispersible granule composition |
| US9095135B2 (en) | 2012-01-12 | 2015-08-04 | Fashion Chemicals, Gmbh & Co. Kg | Microencapsulated volatile insect repellent and/or insecticide agent and methods of making and using the same |
| AU2013293454B2 (en) * | 2012-07-27 | 2017-06-22 | Fmc Corporation | Formulations of clomazone |
| RU2572992C2 (ru) * | 2012-08-28 | 2016-01-20 | Федеральное государственное бюджетное образовательное учреждение высшего образования "Курская государственная сельскохозяйственная академия имени И.И. Иванова" | Способ получения микрокапсул водорастворимых препаратов пестицидов |
| WO2014095889A1 (de) * | 2012-12-17 | 2014-06-26 | Lanxess Deutschland Gmbh | Fungizide silikon-dichtungsmassen |
| WO2014160965A1 (en) * | 2013-03-28 | 2014-10-02 | Rohm And Haas Company | Synergistic combination of a flurochloridone compound and zinc pyrithione for dry film protection |
| KR20150138249A (ko) * | 2013-03-28 | 2015-12-09 | 롬 앤드 하스 캄파니 | 건조막을 보호하기 위한 플루오로클로리돈 화합물과 oit의 상승적 배합물 |
| GB2497901B (en) * | 2013-04-12 | 2016-03-02 | Rotam Agrochem Int Co Ltd | A herbicide composition comprising clomazone encapsulated within cross-linked polyacetylene carbamide-polyurea microcapsules |
| GB2498146B (en) * | 2013-04-15 | 2016-03-16 | Rotam Agrochem Int Co Ltd | A herbicide composition comprising clomazone encapsulated within microcapsules formed by coacervation of amphoteric polymer electrolytes |
| RU2537173C1 (ru) * | 2013-05-24 | 2014-12-27 | Александр Александрович Кролевец | Способ получения микрокапсул гетероциклических соединений триазинового ряда |
| RU2537248C1 (ru) * | 2013-05-24 | 2014-12-27 | Екатерина Евгеньевна Быковская | Способ получения микрокапсул гетероциклических соединений триазинового ряда |
| JP2016527356A (ja) | 2013-07-25 | 2016-09-08 | オーエムジー ユーケイ テクノロジー リミテッド | カプセル化された触媒 |
| US9018327B1 (en) * | 2013-11-08 | 2015-04-28 | Ppg Industries Ohio, Inc. | Catalyst compositions and methods of preparing them |
| CN104738042A (zh) * | 2013-12-26 | 2015-07-01 | 南京华洲药业有限公司 | 含三氟甲吡醚和杀虫环的复合杀虫组合物及其用途 |
| ES2987367T3 (es) | 2014-02-17 | 2024-11-14 | Bayer Cropscience Ag | Derivados de heterociclos bicíclicos condensados sustituidos con 2-(het)arilo como agentes para combatir parásitos |
| GB2509430B (en) | 2014-03-26 | 2016-09-14 | Rotam Agrochem Int Co Ltd | Herbicidal composition, a method for its preparation and the use thereof |
| GB2509429B (en) * | 2014-03-26 | 2016-09-21 | Rotam Agrochem Int Co Ltd | Herbicidal composition, a method for its preparation and the use thereof |
| GB2509428B (en) * | 2014-03-26 | 2016-09-21 | Rotam Agrochem Int Co Ltd | Herbicidal composition, a method for its preparation and the use thereof |
| GB2509427B (en) | 2014-03-26 | 2016-09-21 | Rotam Agrochem Int Co Ltd | Herbicidal composition, a method for its preparation and the use thereof |
| GB2509431B (en) * | 2014-03-26 | 2016-09-14 | Rotam Agrochem Int Co Ltd | Herbicidal composition, a method for its preparation and the use thereof |
| GB2509426B (en) * | 2014-03-26 | 2017-04-26 | Rotam Agrochem Int Co Ltd | Clomazone composition, its preparation and use thereof |
| RU2577598C1 (ru) * | 2015-02-16 | 2016-03-20 | Александр Александрович Кролевец | Способ получения нанокапсул 2,4-дихлорфеноксиуксусной кислоты |
| CN104738081B (zh) * | 2015-02-17 | 2016-06-22 | 中国热带农业科学院热带生物技术研究所 | 一种促进沉香树或白木香树生产沉香的微胶囊及其制备方法和应用 |
| CN104689771B (zh) * | 2015-03-05 | 2017-03-01 | 华南农业大学 | 一种氧化白藜芦醇微胶囊的制备方法及其产品 |
| CN104782623A (zh) * | 2015-03-25 | 2015-07-22 | 塔里木大学 | 一种氟乐灵微囊粒剂及其制备方法 |
| CA2982014A1 (en) * | 2015-04-23 | 2016-10-27 | Basf Se | Agroformulation of microcapsules with sulfonate and codispersant |
| CN107787184B (zh) * | 2015-06-19 | 2021-08-10 | 巴斯夫欧洲公司 | 由四甲基苯二亚甲基二异氰酸酯、脂环族二异氰酸酯和脂族二胺制备的壳的农药微胶囊 |
| ES2800074T3 (es) | 2015-06-19 | 2020-12-23 | Basf Se | Microcápsulas de pendimetalina con una cubierta hecha de diisocianato de tetrametilxilileno y una poliamina con al menos tres grupos amina |
| EP3124556B1 (en) * | 2015-07-31 | 2018-04-18 | Siegwerk Druckfarben AG & Co. KGaA | Water-based inks comprising lignin |
| MX2015010739A (es) * | 2015-08-19 | 2016-01-26 | J Héctor Cabrera Mireles | Sistema de liberacion prolongada para el manejo integrado de plagas agropecuarias, forestales y urbanas. |
| TWI659991B (zh) * | 2015-08-31 | 2019-05-21 | Rohm And Haas Electronic Materials Llc | 與外塗佈光致抗蝕劑一起使用的塗料組合物 |
| EP3205392A1 (en) * | 2016-02-12 | 2017-08-16 | Basf Se | Microcapsules and process for preparation of microcapsules |
| GB2551814B (en) * | 2016-06-30 | 2021-02-24 | Syngenta Participations Ag | Microcapsules encapsulating lambda-cyhalothin |
| EP3511354B1 (en) | 2016-09-06 | 2021-05-05 | FUJIFILM Corporation | Aqueous dispersion, method for producing same, and image forming method |
| MX2019003078A (es) * | 2016-09-16 | 2019-07-08 | Int Flavors & Fragrances Inc | Composiciones de microcapsulas estabilizadas con agentes de control de la viscosidad. |
| US10584074B2 (en) * | 2017-03-17 | 2020-03-10 | Dow Agrosciences Llc | Microencapsulated nitrification inhibitor compositions |
| FR3064192B1 (fr) * | 2017-03-21 | 2019-04-26 | Calyxia | Procede de preparation de capsules comprenant au moins un compose volatile et capsules obtenues |
| FR3064193B1 (fr) * | 2017-03-21 | 2021-04-30 | Calyxia | Procede de preparation de capsules avec des proprietes de retention ameliorees et capsules obtenues |
| CN106942213A (zh) * | 2017-04-12 | 2017-07-14 | 江苏金凤凰农化有限公司 | 一种基于愈创木酚治疗苹果斑点落叶病的组合物及施用方法 |
| CN107258776A (zh) * | 2017-06-29 | 2017-10-20 | 山东大农药业有限公司 | 一种缓释农药颗粒剂及其制备方法 |
| FR3072300B1 (fr) * | 2017-10-16 | 2022-04-22 | Calyxia | Procede de preparation de capsules sensibles au ph ou au rayonnement uv et capsules obtenues |
| CN108575993A (zh) * | 2018-04-19 | 2018-09-28 | 河北威远生物化工有限公司 | 一种草铵膦可分散微囊油悬浮剂及其制备方法 |
| WO2020025566A1 (en) * | 2018-07-31 | 2020-02-06 | Bayer Aktiengesellschaft | Capsule suspensions with agrochemical active ingredients |
| WO2020131866A1 (en) * | 2018-12-18 | 2020-06-25 | International Flavors & Fragrances Inc. | Microcapsule compositions prepared from polysaccharides |
| GB2586771A (en) * | 2018-12-21 | 2021-03-10 | Pangaea Agrochemicals Ltd | Encapsulated pesticide |
| US20220386616A1 (en) | 2019-11-13 | 2022-12-08 | Jesmond Holding Ag | Combination of Encapsulated Phenothrin and Emulsified Prallethrin |
| CN110982031A (zh) * | 2019-11-29 | 2020-04-10 | 合肥科天水性科技有限责任公司 | 一种阳离子水性聚氨酯树脂、其制备方法和在涂料中的用途 |
| EP3845304A1 (en) * | 2019-12-30 | 2021-07-07 | Bayer AG | Capsule suspension concentrates based on polyisocyanates and biodegradable amine based cross-linker |
| CN111514113A (zh) * | 2020-06-11 | 2020-08-11 | 江西农业大学 | 一种母猪口服四烯雌酮微囊的制备方法 |
| CN111718480B (zh) * | 2020-06-30 | 2022-06-10 | 西安近代化学研究所 | 一种端丙烯酰氧基聚醚固化剂 |
| CN112452336B (zh) * | 2020-11-10 | 2024-02-27 | 中国石油化工股份有限公司 | 一种用于丙烯氧化合成丙烯醛的催化剂及其制备方法 |
| BR112023016921A2 (pt) * | 2021-02-23 | 2023-11-28 | Provivi Inc | Feromônios microencapsulados pulverizáveis |
| CN114158804B (zh) * | 2021-11-22 | 2024-05-14 | 鸿瀚防护科技南通有限公司 | 一种可生物降解的功能性环保手套及其制备方法 |
| CN116515074B (zh) * | 2022-04-25 | 2024-04-30 | 江苏奥斯佳材料科技股份有限公司 | 聚氨酯分散体及其制备方法和聚氨酯胶粘剂 |
| CN114794114B (zh) * | 2022-05-31 | 2023-06-09 | 浙江威尔达化工有限公司 | 一种防治水稻病害的农药微囊悬浮剂及其制备方法 |
| CN116688887A (zh) * | 2023-06-28 | 2023-09-05 | 嘉必优生物技术（武汉）股份有限公司 | 一种多不饱和脂肪酸油脂微胶囊及制备方法 |
Family Cites Families (46)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US428720A (en) | 1890-05-27 | Nicke | ||
| US3959464A (en) | 1971-06-03 | 1976-05-25 | Pennwalt Corporation | Microencapsulated methyl and ethyl parathion insecticide in aqueous carrier |
| US3766204A (en) | 1971-06-18 | 1973-10-16 | Allied Chem | Oxyalkylated derivatives of glycolurils |
| US4285720A (en) | 1972-03-15 | 1981-08-25 | Stauffer Chemical Company | Encapsulation process and capsules produced thereby |
| DD108760A1 (enExample) * | 1973-11-02 | 1974-10-05 | ||
| US4056610A (en) * | 1975-04-09 | 1977-11-01 | Minnesota Mining And Manufacturing Company | Microcapsule insecticide composition |
| GB1566297A (en) * | 1975-10-30 | 1980-04-30 | Stauffer Chemical Co | Discrete polyurea microcapsules |
| US4046741A (en) * | 1976-02-17 | 1977-09-06 | Stauffer Chemical Company | Post-treatment of polyurea microcapsules |
| US4118437A (en) | 1976-04-08 | 1978-10-03 | American Cyanamid Company | Cross linkable powder coating compositions |
| DE2633457A1 (de) | 1976-07-24 | 1978-06-08 | Bayer Ag | Verfahren zur herstellung von chemisch nachvernetzten polyurethankunststoffen |
| US4105708A (en) | 1976-09-07 | 1978-08-08 | American Cyanamid Company | Dimethoxymethyl diethoxymethyl glycoluril and coating compositions containing the same as a cross-linking agent |
| US4140516A (en) | 1977-05-31 | 1979-02-20 | Stauffer Chemical Company | Encapsulation process employing phase transfer catalysts |
| DE2738509A1 (de) * | 1977-08-26 | 1979-03-08 | Bayer Ag | Reaktionsdurchschreibepapiere |
| DE2849442A1 (de) | 1978-11-15 | 1980-05-29 | Basf Ag | Verfahren zur herstellung weitgehend reiner pyrazolverbindungen |
| US4280833A (en) | 1979-03-26 | 1981-07-28 | Monsanto Company | Encapsulation by interfacial polycondensation, and aqueous herbicidal composition containing microcapsules produced thereby |
| US4956129A (en) | 1984-03-30 | 1990-09-11 | Ici Americas Inc. | Microencapsulation process |
| US5160529A (en) | 1980-10-30 | 1992-11-03 | Imperial Chemical Industries Plc | Microcapsules and microencapsulation process |
| US4444941A (en) | 1981-05-18 | 1984-04-24 | Scm Corporation | Low temperature cure latexes |
| FR2527061B1 (fr) | 1982-05-19 | 1985-11-15 | Ami | Siege articule |
| US4458036A (en) | 1983-02-28 | 1984-07-03 | Stauffer Chemical Company | Flexible polyurethane foams containing glycoluril reaction products for a flame and ember drip retardance |
| US4534783A (en) * | 1984-01-03 | 1985-08-13 | Monsanto Co. | High concentration encapsulation of water soluble-materials |
| US4643764A (en) | 1984-01-09 | 1987-02-17 | Stauffer Chemical Company | Multiple types of microcapsules and their production |
| JPH0686154B2 (ja) * | 1985-05-08 | 1994-11-02 | 富士写真フイルム株式会社 | 感熱記録材料 |
| DE3635822A1 (de) | 1986-10-22 | 1988-04-28 | Bayer Ag | Mikrokapseln mit waenden aus polyurethan |
| JPH0818937B2 (ja) | 1987-07-06 | 1996-02-28 | 住友化学工業株式会社 | 農園芸用有機燐系殺虫組成物 |
| JPH07106674B2 (ja) * | 1987-09-16 | 1995-11-15 | 富士写真フイルム株式会社 | 感圧記録シート用マイクロカプセル |
| US4837403A (en) * | 1987-12-14 | 1989-06-06 | Basf Aktiengesellschaft | Novel polyalkylpiperidine derivatives having alkylene bridges, use thereof as stabilizers, and intermediates |
| BR9107287A (pt) * | 1991-02-06 | 1994-06-07 | Ici America Inc | Cápsulas capazes de liberaçao controlada de material orgânico encapsulado |
| JPH04265786A (ja) * | 1991-02-20 | 1992-09-21 | Fuji Photo Film Co Ltd | 感圧記録シート用マイクロカプセル |
| US5180835A (en) | 1991-06-25 | 1993-01-19 | American Cyanamid Company | Process for the preparation of monomeric tetramethoxymethylglycoloril |
| JP2630530B2 (ja) * | 1991-11-15 | 1997-07-16 | 株式会社山喜 | オーステナイト系ステンレス線材の処理方法 |
| IL104425A (en) * | 1992-01-22 | 1996-10-31 | Zeneca Ltd | Reducing the content of formaldehyde in tiny capsule preparations |
| JPH05210238A (ja) * | 1992-01-30 | 1993-08-20 | Fuji Photo Film Co Ltd | 感光性マイクロカプセルを含有する感光材料 |
| US5621052A (en) | 1992-12-29 | 1997-04-15 | Cytec Technology Corp. | Aminoplast-anchored ultraviolet light stabilizers |
| DE69529471T2 (de) * | 1994-11-16 | 2003-11-20 | Fmc Corp., Philadelphia | Wenig flüchtige formulierungen von clomazone |
| US5583090A (en) | 1995-06-26 | 1996-12-10 | Monsanto Company | Herbicidal microencapsulated clomazone compositions with reduced vapor transfer |
| AU716712B2 (en) * | 1995-12-29 | 2000-03-02 | Ciba Specialty Chemicals Water Treatments Limited | Particles having a polymeric shell and their production |
| JP3035726B2 (ja) * | 1996-04-26 | 2000-04-24 | 星野化工株式会社 | 含油マイクロカプセル、その製造方法及びマイクロカプセル配合樹脂組成物 |
| US5925595A (en) | 1997-09-05 | 1999-07-20 | Monsanto Company | Microcapsules with readily adjustable release rates |
| US5952595A (en) | 1998-05-12 | 1999-09-14 | Carnell; Richard D. | Chord hand finger conditioner for guitar players |
| US6423425B1 (en) * | 1998-05-26 | 2002-07-23 | Ppg Industries Ohio, Inc. | Article having a chip-resistant electrodeposited coating and a process for forming an electrodeposited coating |
| RU2230606C2 (ru) * | 1998-11-12 | 2004-06-20 | Фмк Корпорейшн | Новый способ получения микрокапсулированных препаратов |
| US6218339B1 (en) | 1999-03-18 | 2001-04-17 | Fmc Corporation | Microencapsulated clomazone in the presence of fat and resin |
| US6485736B1 (en) | 2000-09-07 | 2002-11-26 | Syngenta Ltd. | Variable release microcapsules |
| TWI299101B (en) | 2003-01-30 | 2008-07-21 | Sipix Imaging Inc | High performance capsules for electrophoretic displays |
| US6891012B2 (en) | 2003-05-23 | 2005-05-10 | Bayer Materialscience Llc | Powder coatings produced with crosslinkers capable of curing at low temperatures and coated articles produced therefrom |
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2006
- 2006-03-30 PL PL06006748T patent/PL1840145T3/pl unknown
- 2006-03-30 HU HUE06006748A patent/HUE038015T2/hu unknown
- 2006-03-30 RS RS20180123A patent/RS56792B1/sr unknown
- 2006-03-30 LT LTEP06006748.5T patent/LT1840145T/lt unknown
- 2006-03-30 ES ES06006748.5T patent/ES2659048T3/es active Active
- 2006-03-30 EP EP06006748.5A patent/EP1840145B1/en not_active Revoked
- 2006-03-30 ES ES10011557T patent/ES2864019T3/es active Active
- 2006-03-30 DK DK06006748.5T patent/DK1840145T3/en active
- 2006-03-30 ME MEP-2018-32A patent/ME02956B/me unknown
- 2006-03-30 SI SI200632238T patent/SI1840145T1/en unknown
- 2006-03-30 EP EP10011557.5A patent/EP2487192B1/en not_active Revoked
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2007
- 2007-03-28 US US12/225,890 patent/US8216598B2/en not_active Expired - Fee Related
- 2007-03-29 CN CN2007800203339A patent/CN101460534B/zh not_active Expired - Fee Related
- 2007-03-29 AU AU2007234042A patent/AU2007234042B2/en not_active Ceased
- 2007-03-29 CA CA2647349A patent/CA2647349C/en not_active Expired - Fee Related
- 2007-03-29 JP JP2009501956A patent/JP5523826B2/ja not_active Expired - Fee Related
- 2007-03-29 BR BRPI0710109A patent/BRPI0710109A8/pt not_active Application Discontinuation
- 2007-03-29 UA UAA200812656A patent/UA91750C2/ru unknown
- 2007-03-29 NZ NZ572314A patent/NZ572314A/en not_active IP Right Cessation
- 2007-03-29 MY MYPI20083905A patent/MY165085A/en unknown
- 2007-03-29 CN CN2007800201390A patent/CN101460533B/zh not_active Expired - Fee Related
- 2007-03-29 WO PCT/EP2007/002810 patent/WO2007112934A1/en not_active Ceased
- 2007-03-29 MX MX2008012476A patent/MX2008012476A/es active IP Right Grant
- 2007-03-29 RU RU2008142751/04A patent/RU2443723C2/ru active
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2008
- 2008-09-10 ZA ZA200807779A patent/ZA200807779B/xx unknown
- 2008-09-10 ZA ZA200807778A patent/ZA200807778B/xx unknown
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2012
- 2012-06-05 US US13/489,208 patent/US8828415B2/en not_active Expired - Fee Related
-
2018
- 2018-02-07 HR HRP20180231TT patent/HRP20180231T1/hr unknown
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