UA78063C2 - Herbicidal composition and method to control weeds - Google Patents
Herbicidal composition and method to control weeds Download PDFInfo
- Publication number
- UA78063C2 UA78063C2 UAA200500284A UA2005000284A UA78063C2 UA 78063 C2 UA78063 C2 UA 78063C2 UA A200500284 A UAA200500284 A UA A200500284A UA 2005000284 A UA2005000284 A UA 2005000284A UA 78063 C2 UA78063 C2 UA 78063C2
- Authority
- UA
- Ukraine
- Prior art keywords
- alkyl
- carbon atoms
- group
- herbicidal composition
- formula
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 67
- 230000002363 herbicidal effect Effects 0.000 title claims abstract description 34
- 241000196324 Embryophyta Species 0.000 title claims description 22
- 238000000034 method Methods 0.000 title claims description 5
- 239000004009 herbicide Substances 0.000 claims abstract description 20
- UEZVMMHDMIWARA-UHFFFAOYSA-M phosphonate Chemical compound [O-]P(=O)=O UEZVMMHDMIWARA-UHFFFAOYSA-M 0.000 claims abstract description 19
- ACVYVLVWPXVTIT-UHFFFAOYSA-M phosphinate Chemical compound [O-][PH2]=O ACVYVLVWPXVTIT-UHFFFAOYSA-M 0.000 claims abstract description 16
- 229910019142 PO4 Inorganic materials 0.000 claims abstract description 15
- -1 2-(substituted benzoyl)-1.3- cyclohexanedione Chemical class 0.000 claims abstract description 14
- 239000010452 phosphate Substances 0.000 claims abstract description 14
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 claims abstract description 14
- 239000007921 spray Substances 0.000 claims abstract description 12
- 239000002671 adjuvant Substances 0.000 claims abstract description 5
- 125000000217 alkyl group Chemical group 0.000 claims description 67
- 125000004432 carbon atom Chemical group C* 0.000 claims description 39
- 150000001875 compounds Chemical class 0.000 claims description 24
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 14
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 11
- 125000005843 halogen group Chemical group 0.000 claims description 10
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 10
- 125000003342 alkenyl group Chemical group 0.000 claims description 8
- 125000001188 haloalkyl group Chemical group 0.000 claims description 8
- 239000000126 substance Substances 0.000 claims description 7
- 239000001257 hydrogen Substances 0.000 claims description 6
- 229910052739 hydrogen Inorganic materials 0.000 claims description 6
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 claims description 5
- 229910052736 halogen Inorganic materials 0.000 claims description 5
- 150000002367 halogens Chemical class 0.000 claims description 5
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 4
- 125000003545 alkoxy group Chemical group 0.000 claims description 4
- 125000003806 alkyl carbonyl amino group Chemical group 0.000 claims description 4
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Chemical group BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 4
- 229910052794 bromium Inorganic materials 0.000 claims description 4
- 239000000460 chlorine Substances 0.000 claims description 4
- 229910052801 chlorine Inorganic materials 0.000 claims description 4
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 4
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 4
- 125000001424 substituent group Chemical group 0.000 claims description 3
- JHNVAGCOUOBGJS-UHFFFAOYSA-N 2-(2-chloro-3-ethoxy-4-ethylsulfonylbenzoyl)-5-methylcyclohexane-1,3-dione Chemical compound C1=C(S(=O)(=O)CC)C(OCC)=C(Cl)C(C(=O)C2C(CC(C)CC2=O)=O)=C1 JHNVAGCOUOBGJS-UHFFFAOYSA-N 0.000 claims description 2
- OIRQAQLOHBJUIA-UHFFFAOYSA-N 2-(2-chloro-3-ethoxy-4-methylsulfonylbenzoyl)-5-methylcyclohexane-1,3-dione Chemical compound C1=C(S(C)(=O)=O)C(OCC)=C(Cl)C(C(=O)C2C(CC(C)CC2=O)=O)=C1 OIRQAQLOHBJUIA-UHFFFAOYSA-N 0.000 claims description 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 2
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims description 2
- 125000004949 alkyl amino carbonyl amino group Chemical group 0.000 claims description 2
- 125000005195 alkyl amino carbonyloxy group Chemical group 0.000 claims description 2
- 125000003282 alkyl amino group Chemical group 0.000 claims description 2
- 125000004448 alkyl carbonyl group Chemical group 0.000 claims description 2
- 125000005196 alkyl carbonyloxy group Chemical group 0.000 claims description 2
- 125000000304 alkynyl group Chemical group 0.000 claims description 2
- 125000004429 atom Chemical group 0.000 claims description 2
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 2
- 125000001309 chloro group Chemical group Cl* 0.000 claims description 2
- 125000004966 cyanoalkyl group Chemical group 0.000 claims description 2
- 125000004663 dialkyl amino group Chemical group 0.000 claims description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 2
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims description 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 2
- IWLCLWRHQGUHCH-UHFFFAOYSA-N 4,4-dimethyl-2-(4-methylsulfonyl-2-nitrobenzoyl)cyclohexane-1,3-dione Chemical compound O=C1C(C)(C)CCC(=O)C1C(=O)C1=CC=C(S(C)(=O)=O)C=C1[N+]([O-])=O IWLCLWRHQGUHCH-UHFFFAOYSA-N 0.000 claims 1
- 125000005194 alkoxycarbonyloxy group Chemical group 0.000 claims 1
- 238000012876 topography Methods 0.000 claims 1
- 239000000654 additive Substances 0.000 abstract 1
- 230000000996 additive effect Effects 0.000 abstract 1
- 239000002253 acid Substances 0.000 description 11
- 235000021317 phosphate Nutrition 0.000 description 11
- 239000012141 concentrate Substances 0.000 description 10
- 239000007788 liquid Substances 0.000 description 10
- 239000004480 active ingredient Substances 0.000 description 9
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 9
- 239000000546 pharmaceutical excipient Substances 0.000 description 8
- GOCVCBDBQYEFQD-UHFFFAOYSA-N 3-[[2-ethylhexoxy(2-ethylhexyl)phosphoryl]oxymethyl]heptane Chemical compound CCCCC(CC)COP(=O)(CC(CC)CCCC)OCC(CC)CCCC GOCVCBDBQYEFQD-UHFFFAOYSA-N 0.000 description 6
- 239000000843 powder Substances 0.000 description 6
- 230000000694 effects Effects 0.000 description 5
- 239000007787 solid Substances 0.000 description 5
- 230000006378 damage Effects 0.000 description 4
- 239000002270 dispersing agent Substances 0.000 description 4
- 239000003995 emulsifying agent Substances 0.000 description 4
- 239000003921 oil Substances 0.000 description 4
- 235000019198 oils Nutrition 0.000 description 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
- 240000008042 Zea mays Species 0.000 description 3
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 3
- 239000000969 carrier Substances 0.000 description 3
- 239000004927 clay Substances 0.000 description 3
- 239000004615 ingredient Substances 0.000 description 3
- 239000003960 organic solvent Substances 0.000 description 3
- 239000002245 particle Substances 0.000 description 3
- 239000004094 surface-active agent Substances 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- 101100149549 Arabidopsis thaliana SKOR gene Proteins 0.000 description 2
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 2
- ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical class OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 description 2
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 235000005822 corn Nutrition 0.000 description 2
- 238000007865 diluting Methods 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- 239000004495 emulsifiable concentrate Substances 0.000 description 2
- 239000008187 granular material Substances 0.000 description 2
- 229910003480 inorganic solid Inorganic materials 0.000 description 2
- HJOVHMDZYOCNQW-UHFFFAOYSA-N isophorone Chemical compound CC1=CC(=O)CC(C)(C)C1 HJOVHMDZYOCNQW-UHFFFAOYSA-N 0.000 description 2
- KPUREKXXPHOJQT-UHFFFAOYSA-N mesotrione Chemical compound [O-][N+](=O)C1=CC(S(=O)(=O)C)=CC=C1C(=O)C1C(=O)CCCC1=O KPUREKXXPHOJQT-UHFFFAOYSA-N 0.000 description 2
- 239000002689 soil Substances 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 239000000725 suspension Substances 0.000 description 2
- 239000004546 suspension concentrate Substances 0.000 description 2
- STCOOQWBFONSKY-UHFFFAOYSA-N tributyl phosphate Chemical compound CCCCOP(=O)(OCCCC)OCCCC STCOOQWBFONSKY-UHFFFAOYSA-N 0.000 description 2
- 235000015112 vegetable and seed oil Nutrition 0.000 description 2
- 238000009736 wetting Methods 0.000 description 2
- 239000000080 wetting agent Substances 0.000 description 2
- 239000008096 xylene Substances 0.000 description 2
- JPGXOMADPRULAC-UHFFFAOYSA-N 1-[butoxy(butyl)phosphoryl]oxybutane Chemical compound CCCCOP(=O)(CCCC)OCCCC JPGXOMADPRULAC-UHFFFAOYSA-N 0.000 description 1
- PAWQVTBBRAZDMG-UHFFFAOYSA-N 2-(3-bromo-2-fluorophenyl)acetic acid Chemical compound OC(=O)CC1=CC=CC(Br)=C1F PAWQVTBBRAZDMG-UHFFFAOYSA-N 0.000 description 1
- 239000005995 Aluminium silicate Substances 0.000 description 1
- 239000005503 Desmedipham Substances 0.000 description 1
- 229920001353 Dextrin Polymers 0.000 description 1
- 239000004375 Dextrin Substances 0.000 description 1
- 239000005572 Lenacil Substances 0.000 description 1
- 239000005579 Metamitron Substances 0.000 description 1
- 239000005662 Paraffin oil Substances 0.000 description 1
- 239000005594 Phenmedipham Substances 0.000 description 1
- GTVWRXDRKAHEAD-UHFFFAOYSA-N Tris(2-ethylhexyl) phosphate Chemical compound CCCCC(CC)COP(=O)(OCC(CC)CCCC)OCC(CC)CCCC GTVWRXDRKAHEAD-UHFFFAOYSA-N 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
- 235000016383 Zea mays subsp huehuetenangensis Nutrition 0.000 description 1
- MAPXZHNGBCCSFO-UHFFFAOYSA-N [4-(2,6-dioxocyclohexanecarbonyl)-3-nitrophenyl] methanesulfonate Chemical compound [O-][N+](=O)C1=CC(OS(=O)(=O)C)=CC=C1C(=O)C1C(=O)CCCC1=O MAPXZHNGBCCSFO-UHFFFAOYSA-N 0.000 description 1
- 239000012190 activator Substances 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 239000000443 aerosol Substances 0.000 description 1
- 150000008055 alkyl aryl sulfonates Chemical class 0.000 description 1
- 230000029936 alkylation Effects 0.000 description 1
- 238000005804 alkylation reaction Methods 0.000 description 1
- JZQOJFLIJNRDHK-CMDGGOBGSA-N alpha-irone Chemical compound CC1CC=C(C)C(\C=C\C(C)=O)C1(C)C JZQOJFLIJNRDHK-CMDGGOBGSA-N 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- BFNBIHQBYMNNAN-UHFFFAOYSA-N ammonium sulfate Chemical compound N.N.OS(O)(=O)=O BFNBIHQBYMNNAN-UHFFFAOYSA-N 0.000 description 1
- 229910052921 ammonium sulfate Inorganic materials 0.000 description 1
- 235000011130 ammonium sulphate Nutrition 0.000 description 1
- 229960000892 attapulgite Drugs 0.000 description 1
- 239000010427 ball clay Substances 0.000 description 1
- 239000000440 bentonite Substances 0.000 description 1
- 229910000278 bentonite Inorganic materials 0.000 description 1
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 1
- 230000003115 biocidal effect Effects 0.000 description 1
- 239000003139 biocide Substances 0.000 description 1
- 230000004791 biological behavior Effects 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 239000013043 chemical agent Substances 0.000 description 1
- WYKYKTKDBLFHCY-UHFFFAOYSA-N chloridazon Chemical compound O=C1C(Cl)=C(N)C=NN1C1=CC=CC=C1 WYKYKTKDBLFHCY-UHFFFAOYSA-N 0.000 description 1
- WZJZMXBKUWKXTQ-UHFFFAOYSA-N desmedipham Chemical compound CCOC(=O)NC1=CC=CC(OC(=O)NC=2C=CC=CC=2)=C1 WZJZMXBKUWKXTQ-UHFFFAOYSA-N 0.000 description 1
- 235000019425 dextrin Nutrition 0.000 description 1
- GUJOJGAPFQRJSV-UHFFFAOYSA-N dialuminum;dioxosilane;oxygen(2-);hydrate Chemical compound O.[O-2].[O-2].[O-2].[Al+3].[Al+3].O=[Si]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O GUJOJGAPFQRJSV-UHFFFAOYSA-N 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 230000001804 emulsifying effect Effects 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 125000004185 ester group Chemical group 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 239000003337 fertilizer Substances 0.000 description 1
- 235000013312 flour Nutrition 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 230000014509 gene expression Effects 0.000 description 1
- 239000003292 glue Substances 0.000 description 1
- 230000005764 inhibitory process Effects 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- 239000011147 inorganic material Substances 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- 239000003350 kerosene Substances 0.000 description 1
- ZTMKADLOSYKWCA-UHFFFAOYSA-N lenacil Chemical compound O=C1NC=2CCCC=2C(=O)N1C1CCCCC1 ZTMKADLOSYKWCA-UHFFFAOYSA-N 0.000 description 1
- 235000009973 maize Nutrition 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- VHCNQEUWZYOAEV-UHFFFAOYSA-N metamitron Chemical compound O=C1N(N)C(C)=NN=C1C1=CC=CC=C1 VHCNQEUWZYOAEV-UHFFFAOYSA-N 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 150000002790 naphthalenes Chemical class 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- 239000011368 organic material Substances 0.000 description 1
- 125000001820 oxy group Chemical group [*:1]O[*:2] 0.000 description 1
- 229910052625 palygorskite Inorganic materials 0.000 description 1
- 239000010451 perlite Substances 0.000 description 1
- 235000019362 perlite Nutrition 0.000 description 1
- 239000003208 petroleum Substances 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
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 230000001629 suppression Effects 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 239000010455 vermiculite Substances 0.000 description 1
- 229910052902 vermiculite Inorganic materials 0.000 description 1
- 235000019354 vermiculite Nutrition 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
- A01N41/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a sulfur atom bound to a hetero atom
- A01N41/02—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a sulfur atom bound to a hetero atom containing a sulfur-to-oxygen double bond
- A01N41/10—Sulfones; Sulfoxides
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GBGB0213638.0A GB0213638D0 (en) | 2002-06-13 | 2002-06-13 | Composition |
| PCT/GB2003/002428 WO2003105589A1 (en) | 2002-06-13 | 2003-06-04 | Composition comprising a cyclohexanedione herbicide and an adjuvant |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| UA78063C2 true UA78063C2 (en) | 2007-02-15 |
Family
ID=9938540
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| UAA200500284A UA78063C2 (en) | 2002-06-13 | 2003-04-06 | Herbicidal composition and method to control weeds |
Country Status (14)
| Country | Link |
|---|---|
| US (2) | US20050202975A1 (pt) |
| EP (1) | EP1515608A1 (pt) |
| JP (1) | JP2005529174A (pt) |
| CN (1) | CN1658756A (pt) |
| AU (1) | AU2003232935A1 (pt) |
| BR (1) | BR0311717A (pt) |
| CA (1) | CA2484544A1 (pt) |
| GB (1) | GB0213638D0 (pt) |
| MX (1) | MXPA04012284A (pt) |
| PL (1) | PL372765A1 (pt) |
| RS (1) | RS103304A (pt) |
| UA (1) | UA78063C2 (pt) |
| WO (1) | WO2003105589A1 (pt) |
| ZA (1) | ZA200408510B (pt) |
Families Citing this family (43)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8114426B2 (en) * | 2005-07-19 | 2012-02-14 | Oms Investments, Inc. | Granular turf safe mesotrione compositions |
| CN101600882A (zh) * | 2006-01-20 | 2009-12-09 | 西南风力公司 | 风力涡轮机的失速控制器以及触发条件的控制装置 |
| GB0621440D0 (en) * | 2006-10-27 | 2006-12-06 | Syngenta Crop Protection Ag | Herbicidal compositions |
| JP5390801B2 (ja) | 2007-07-13 | 2014-01-15 | 石原産業株式会社 | 除草性組成物 |
| GB0715576D0 (en) * | 2007-08-09 | 2007-09-19 | Syngenta Ltd | Novel herbicides |
| US20090062911A1 (en) * | 2007-08-27 | 2009-03-05 | Amo Groningen Bv | Multizonal lens with extended depth of focus |
| US8974526B2 (en) | 2007-08-27 | 2015-03-10 | Amo Groningen B.V. | Multizonal lens with extended depth of focus |
| US8740978B2 (en) * | 2007-08-27 | 2014-06-03 | Amo Regional Holdings | Intraocular lens having extended depth of focus |
| US9216080B2 (en) | 2007-08-27 | 2015-12-22 | Amo Groningen B.V. | Toric lens with decreased sensitivity to cylinder power and rotation and method of using the same |
| US8747466B2 (en) * | 2007-08-27 | 2014-06-10 | Amo Groningen, B.V. | Intraocular lens having extended depth of focus |
| US8288320B2 (en) | 2007-10-04 | 2012-10-16 | Oms Investments, Inc. | Methods for preparing granular weed control products having improved distribution of agriculturally active ingredients coated thereon |
| CA2715537C (en) | 2008-02-15 | 2016-09-06 | Amo Regional Holdings | System, ophthalmic lens, and method for extending depth of focus |
| US8439498B2 (en) | 2008-02-21 | 2013-05-14 | Abbott Medical Optics Inc. | Toric intraocular lens with modified power characteristics |
| US8231219B2 (en) * | 2008-04-24 | 2012-07-31 | Amo Groningen B.V. | Diffractive lens exhibiting enhanced optical performance |
| US7871162B2 (en) * | 2008-04-24 | 2011-01-18 | Amo Groningen B.V. | Diffractive multifocal lens having radially varying light distribution |
| US8862447B2 (en) | 2010-04-30 | 2014-10-14 | Amo Groningen B.V. | Apparatus, system and method for predictive modeling to design, evaluate and optimize ophthalmic lenses |
| US9335563B2 (en) | 2012-08-31 | 2016-05-10 | Amo Groningen B.V. | Multi-ring lens, systems and methods for extended depth of focus |
| GB0819205D0 (en) * | 2008-10-20 | 2008-11-26 | Syngenta Ltd | Novel herbicides |
| EP2193712A1 (de) * | 2008-12-05 | 2010-06-09 | Bayer CropScience AG | Dispersionen enthaltend Inhibitoren der Hydroxyphenylpyruvat-Dioxygenase |
| EP2512370B1 (en) | 2009-12-18 | 2020-10-21 | AMO Groningen B.V. | Limited echelette lens |
| US9817246B2 (en) | 2010-12-01 | 2017-11-14 | Amo Groningen B.V. | Multifocal lens having an optical add power progression, and a system and method of providing same |
| US9931200B2 (en) | 2010-12-17 | 2018-04-03 | Amo Groningen B.V. | Ophthalmic devices, systems, and methods for optimizing peripheral vision |
| US8894204B2 (en) | 2010-12-17 | 2014-11-25 | Abbott Medical Optics Inc. | Ophthalmic lens, systems and methods having at least one rotationally asymmetric diffractive structure |
| EP2928413B1 (en) | 2012-12-04 | 2019-08-14 | AMO Groningen B.V. | Lenses systems and methods for providing binocular customized treatments to correct presbyopia |
| AU2014228357B2 (en) | 2013-03-11 | 2018-08-23 | Johnson & Johnson Surgical Vision, Inc. | Intraocular lens that matches an image surface to a retinal shape, and method of designing same |
| CA2942198C (en) | 2014-03-10 | 2023-08-01 | Amo Groningen B.V. | Enhanced toric lens that improves overall vision where there is a local loss of retinal function |
| CA2946356C (en) | 2014-04-21 | 2022-09-20 | Amo Groningen B.V. | Ophthalmic devices, system and methods that improve peripheral vision |
| EP3413841A1 (en) | 2016-02-09 | 2018-12-19 | AMO Groningen B.V. | Progressive power intraocular lens, and methods of use and manufacture |
| WO2017153843A1 (en) | 2016-03-11 | 2017-09-14 | Amo Groningen B.V. | Intraocular lenses that improve peripheral vision |
| EP3433667B1 (en) | 2016-03-23 | 2022-09-28 | Johnson & Johnson Surgical Vision, Inc. | Ophthalmic apparatus with corrective meridians having extended tolerance band with freeform refractive surfaces |
| CA3018545A1 (en) | 2016-03-23 | 2017-09-28 | Johnson & Johnson Surgical Vision, Inc. | Power calculator for an ophthalmic apparatus with corrective meridians having extended tolerance or operation band |
| WO2017182878A1 (en) | 2016-04-19 | 2017-10-26 | Amo Groningen B.V. | Ophthalmic devices, system and methods that improve peripheral vision |
| WO2018078439A2 (en) | 2016-10-25 | 2018-05-03 | Amo Groningen B.V. | Realistic eye models to design and evaluate intraocular lenses for a large field of view |
| AU2018235011A1 (en) | 2017-03-17 | 2019-10-24 | Amo Groningen B.V. | Diffractive intraocular lenses for extended range of vision |
| US10739227B2 (en) | 2017-03-23 | 2020-08-11 | Johnson & Johnson Surgical Vision, Inc. | Methods and systems for measuring image quality |
| US11523897B2 (en) | 2017-06-23 | 2022-12-13 | Amo Groningen B.V. | Intraocular lenses for presbyopia treatment |
| US11262598B2 (en) | 2017-06-28 | 2022-03-01 | Amo Groningen, B.V. | Diffractive lenses and related intraocular lenses for presbyopia treatment |
| EP3639084A1 (en) | 2017-06-28 | 2020-04-22 | Amo Groningen B.V. | Extended range and related intraocular lenses for presbyopia treatment |
| US11327210B2 (en) | 2017-06-30 | 2022-05-10 | Amo Groningen B.V. | Non-repeating echelettes and related intraocular lenses for presbyopia treatment |
| CA3082053A1 (en) | 2017-11-30 | 2019-06-06 | Amo Groningen B.V. | Intraocular lenses that improve post-surgical spectacle independent and methods of manufacturing thereof |
| TW202126173A (zh) * | 2019-10-03 | 2021-07-16 | 美商富曼西公司 | 二醯胺殺蟲劑組合物 |
| AU2020416055A1 (en) | 2019-12-30 | 2022-08-25 | Amo Groningen B.V. | Lenses having diffractive profiles with irregular width for vision treatment |
| US11886046B2 (en) | 2019-12-30 | 2024-01-30 | Amo Groningen B.V. | Multi-region refractive lenses for vision treatment |
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| Publication number | Priority date | Publication date | Assignee | Title |
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| US2927014A (en) * | 1957-02-14 | 1960-03-01 | Virginia Carolina Chem Corp | Method for killing plants |
| US5006158A (en) * | 1984-12-20 | 1991-04-09 | Ici Americas Inc. | Certain 2-(2-substituted benzoyl)-1,3-cyclohexanediones |
| US4462972A (en) * | 1982-07-19 | 1984-07-31 | Cf Industries, Inc. | Method for producing fertilizer-grade phosphoric acid |
| US4776882A (en) * | 1982-12-27 | 1988-10-11 | Rhone Poulenc Nederlands B.V. | Concentrated basal spray |
| US4938796A (en) * | 1987-07-06 | 1990-07-03 | Ici Americas Inc. | Herbicidal compositions of acylated 1,3-dicarbonyl herbicides and antidotes therefor |
| US5089046A (en) * | 1988-04-04 | 1992-02-18 | Sandoz Ltd. | Aryl and heteroaryl diones |
| US5428001A (en) * | 1988-11-10 | 1995-06-27 | Regents Of The University Of Minnesota | Method for combating weeds among maize plants |
| GB9118565D0 (en) * | 1991-08-30 | 1991-10-16 | Schering Ag | Herbicidal compositions |
| DE4319263A1 (de) * | 1992-07-03 | 1994-01-05 | Schoenherr Joerg | Pflanzenbehandlungsmittel |
| DE4305542C1 (de) * | 1993-02-20 | 1994-07-21 | Schering Ag | Herbizide Mittel mit synergistischer Wirkung |
| US5877112A (en) * | 1997-08-27 | 1999-03-02 | Helena Chemical Company | Agricultural formulation |
| WO2001043550A2 (en) * | 1999-12-17 | 2001-06-21 | Aventis Cropscience S.A. | Method of controlling weeds |
| IL153006A0 (en) * | 2000-06-13 | 2003-06-24 | Syngenta Ltd | Method for improving the selectivity of 1,3-cyclohexanedione herbicide |
| IL154478A0 (en) * | 2000-09-08 | 2003-09-17 | Syngenta Participations Ag | Mesotrione formulations |
| US6890889B1 (en) * | 2000-09-08 | 2005-05-10 | Syngenta Crop Protection, Inc. | Mesotrione formulations |
| GB0022835D0 (en) * | 2000-09-18 | 2000-11-01 | Aventis Cropscience Sa | New herbicidal composition |
| US8114426B2 (en) * | 2005-07-19 | 2012-02-14 | Oms Investments, Inc. | Granular turf safe mesotrione compositions |
-
2002
- 2002-06-13 GB GBGB0213638.0A patent/GB0213638D0/en not_active Ceased
-
2003
- 2003-04-06 UA UAA200500284A patent/UA78063C2/uk unknown
- 2003-06-04 AU AU2003232935A patent/AU2003232935A1/en not_active Abandoned
- 2003-06-04 CA CA002484544A patent/CA2484544A1/en not_active Abandoned
- 2003-06-04 EP EP03727734A patent/EP1515608A1/en not_active Withdrawn
- 2003-06-04 RS YUP-1033/04A patent/RS103304A/sr unknown
- 2003-06-04 MX MXPA04012284A patent/MXPA04012284A/es not_active Application Discontinuation
- 2003-06-04 WO PCT/GB2003/002428 patent/WO2003105589A1/en active Application Filing
- 2003-06-04 JP JP2004512508A patent/JP2005529174A/ja active Pending
- 2003-06-04 US US10/517,873 patent/US20050202975A1/en not_active Abandoned
- 2003-06-04 BR BR0311717-0A patent/BR0311717A/pt not_active IP Right Cessation
- 2003-06-04 PL PL03372765A patent/PL372765A1/xx not_active Application Discontinuation
- 2003-06-04 CN CN03813521.3A patent/CN1658756A/zh active Pending
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2004
- 2004-10-20 ZA ZA200408510A patent/ZA200408510B/xx unknown
- 2004-12-01 US US11/000,700 patent/US20050096226A1/en not_active Abandoned
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| Publication number | Publication date |
|---|---|
| WO2003105589A1 (en) | 2003-12-24 |
| MXPA04012284A (es) | 2005-02-25 |
| PL372765A1 (en) | 2005-08-08 |
| RS103304A (en) | 2007-02-05 |
| EP1515608A1 (en) | 2005-03-23 |
| CA2484544A1 (en) | 2003-12-24 |
| CN1658756A (zh) | 2005-08-24 |
| US20050096226A1 (en) | 2005-05-05 |
| JP2005529174A (ja) | 2005-09-29 |
| AU2003232935A1 (en) | 2003-12-31 |
| BR0311717A (pt) | 2005-03-01 |
| ZA200408510B (en) | 2005-10-13 |
| US20050202975A1 (en) | 2005-09-15 |
| GB0213638D0 (en) | 2002-07-24 |
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