ZA200304946B - Paste formulation for seed treatment of plants. - Google Patents
Paste formulation for seed treatment of plants. Download PDFInfo
- Publication number
- ZA200304946B ZA200304946B ZA200304946A ZA200304946A ZA200304946B ZA 200304946 B ZA200304946 B ZA 200304946B ZA 200304946 A ZA200304946 A ZA 200304946A ZA 200304946 A ZA200304946 A ZA 200304946A ZA 200304946 B ZA200304946 B ZA 200304946B
- Authority
- ZA
- South Africa
- Prior art keywords
- composition
- group
- carbon atoms
- methyl
- alkyl
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims description 66
- 238000009472 formulation Methods 0.000 title claims description 35
- 238000011282 treatment Methods 0.000 title claims description 22
- 125000004432 carbon atom Chemical group C* 0.000 claims description 18
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical group C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims description 13
- -1 methylcarbamic acid 2-(2-chloro-1- methoxy ethoxy) phenyl ester Chemical class 0.000 claims description 13
- 125000000217 alkyl group Chemical group 0.000 claims description 12
- 239000002270 dispersing agent Substances 0.000 claims description 10
- 229910052739 hydrogen Inorganic materials 0.000 claims description 10
- 239000000049 pigment Substances 0.000 claims description 9
- 150000002430 hydrocarbons Chemical group 0.000 claims description 8
- 239000001257 hydrogen Substances 0.000 claims description 8
- 125000002947 alkylene group Chemical group 0.000 claims description 7
- 239000000654 additive Substances 0.000 claims description 6
- 239000004615 ingredient Substances 0.000 claims description 6
- 239000004094 surface-active agent Substances 0.000 claims description 6
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 5
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical group CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 claims description 5
- 229920001296 polysiloxane Polymers 0.000 claims description 5
- 239000004215 Carbon black (E152) Substances 0.000 claims description 4
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical group C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 claims description 4
- 230000000996 additive effect Effects 0.000 claims description 4
- 239000003795 chemical substances by application Substances 0.000 claims description 4
- KQTVWCSONPJJPE-UHFFFAOYSA-N etridiazole Chemical compound CCOC1=NC(C(Cl)(Cl)Cl)=NS1 KQTVWCSONPJJPE-UHFFFAOYSA-N 0.000 claims description 4
- 229930195733 hydrocarbon Natural products 0.000 claims description 4
- 239000003921 oil Substances 0.000 claims description 4
- AMEKQAFGQBKLKX-UHFFFAOYSA-N oxycarboxin Chemical compound O=S1(=O)CCOC(C)=C1C(=O)NC1=CC=CC=C1 AMEKQAFGQBKLKX-UHFFFAOYSA-N 0.000 claims description 4
- LKPLKUMXSAEKID-UHFFFAOYSA-N pentachloronitrobenzene Chemical compound [O-][N+](=O)C1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1Cl LKPLKUMXSAEKID-UHFFFAOYSA-N 0.000 claims description 4
- 125000000218 acetic acid group Chemical group C(C)(=O)* 0.000 claims description 3
- DUEPRVBVGDRKAG-UHFFFAOYSA-N carbofuran Chemical compound CNC(=O)OC1=CC=CC2=C1OC(C)(C)C2 DUEPRVBVGDRKAG-UHFFFAOYSA-N 0.000 claims description 3
- 150000002431 hydrogen Chemical class 0.000 claims description 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 3
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 claims description 3
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 claims description 3
- WJCNZQLZVWNLKY-UHFFFAOYSA-N thiabendazole Chemical compound S1C=NC(C=2NC3=CC=CC=C3N=2)=C1 WJCNZQLZVWNLKY-UHFFFAOYSA-N 0.000 claims description 3
- KUAZQDVKQLNFPE-UHFFFAOYSA-N thiram Chemical compound CN(C)C(=S)SSC(=S)N(C)C KUAZQDVKQLNFPE-UHFFFAOYSA-N 0.000 claims description 3
- 229960002447 thiram Drugs 0.000 claims description 3
- 244000063299 Bacillus subtilis Species 0.000 claims description 2
- 235000014469 Bacillus subtilis Nutrition 0.000 claims description 2
- SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 claims description 2
- 241000228143 Penicillium Species 0.000 claims description 2
- 241000589187 Rhizobium sp. Species 0.000 claims description 2
- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 2
- 125000002889 tridecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 2
- 229920005610 lignin Polymers 0.000 claims 4
- 125000001273 sulfonato group Chemical class [O-]S(*)(=O)=O 0.000 claims 4
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 claims 3
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical group C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 claims 3
- 235000019198 oils Nutrition 0.000 claims 3
- 239000013543 active substance Substances 0.000 claims 2
- 235000010290 biphenyl Nutrition 0.000 claims 2
- MCVUKOYZUCWLQQ-UHFFFAOYSA-N tridecylbenzene Chemical compound CCCCCCCCCCCCCC1=CC=CC=C1 MCVUKOYZUCWLQQ-UHFFFAOYSA-N 0.000 claims 2
- ZQEIXNIJLIKNTD-LBPRGKRZSA-N (S)-metalaxyl Chemical compound COCC(=O)N([C@@H](C)C(=O)OC)C1=C(C)C=CC=C1C ZQEIXNIJLIKNTD-LBPRGKRZSA-N 0.000 claims 1
- PXMNMQRDXWABCY-UHFFFAOYSA-N 1-(4-chlorophenyl)-4,4-dimethyl-3-(1H-1,2,4-triazol-1-ylmethyl)pentan-3-ol Chemical compound C1=NC=NN1CC(O)(C(C)(C)C)CCC1=CC=C(Cl)C=C1 PXMNMQRDXWABCY-UHFFFAOYSA-N 0.000 claims 1
- WBIQQQGBSDOWNP-UHFFFAOYSA-N 2-dodecylbenzenesulfonic acid Chemical compound CCCCCCCCCCCCC1=CC=CC=C1S(O)(=O)=O WBIQQQGBSDOWNP-UHFFFAOYSA-N 0.000 claims 1
- BCFOOQRXUXKJCL-UHFFFAOYSA-N 4-amino-4-oxo-2-sulfobutanoic acid Chemical class NC(=O)CC(C(O)=O)S(O)(=O)=O BCFOOQRXUXKJCL-UHFFFAOYSA-N 0.000 claims 1
- 239000005746 Carboxin Substances 0.000 claims 1
- BTANRVKWQNVYAZ-UHFFFAOYSA-N Sec-butyl alcohol Natural products CCC(C)O BTANRVKWQNVYAZ-UHFFFAOYSA-N 0.000 claims 1
- 229920002125 Sokalan® Polymers 0.000 claims 1
- ULUAUXLGCMPNKK-UHFFFAOYSA-N Sulfobutanedioic acid Chemical class OC(=O)CC(C(O)=O)S(O)(=O)=O ULUAUXLGCMPNKK-UHFFFAOYSA-N 0.000 claims 1
- 239000005839 Tebuconazole Substances 0.000 claims 1
- 150000001298 alcohols Chemical class 0.000 claims 1
- 239000004305 biphenyl Substances 0.000 claims 1
- 125000006267 biphenyl group Chemical group 0.000 claims 1
- GYSSRZJIHXQEHQ-UHFFFAOYSA-N carboxin Chemical compound S1CCOC(C)=C1C(=O)NC1=CC=CC=C1 GYSSRZJIHXQEHQ-UHFFFAOYSA-N 0.000 claims 1
- 229940060296 dodecylbenzenesulfonic acid Drugs 0.000 claims 1
- YWTYJOPNNQFBPC-UHFFFAOYSA-N imidacloprid Chemical compound [O-][N+](=O)\N=C1/NCCN1CC1=CC=C(Cl)N=C1 YWTYJOPNNQFBPC-UHFFFAOYSA-N 0.000 claims 1
- 239000002480 mineral oil Substances 0.000 claims 1
- 235000010446 mineral oil Nutrition 0.000 claims 1
- 150000002790 naphthalenes Chemical class 0.000 claims 1
- 239000003208 petroleum Substances 0.000 claims 1
- 239000004584 polyacrylic acid Substances 0.000 claims 1
- 229920000642 polymer Polymers 0.000 claims 1
- 235000015112 vegetable and seed oil Nutrition 0.000 claims 1
- 239000008158 vegetable oil Substances 0.000 claims 1
- JLYXXMFPNIAWKQ-UHFFFAOYSA-N γ Benzene hexachloride Chemical compound ClC1C(Cl)C(Cl)C(Cl)C(Cl)C1Cl JLYXXMFPNIAWKQ-UHFFFAOYSA-N 0.000 claims 1
- 241000196324 Embryophyta Species 0.000 description 11
- 238000000576 coating method Methods 0.000 description 7
- 239000000975 dye Substances 0.000 description 7
- 239000011248 coating agent Substances 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- 239000004480 active ingredient Substances 0.000 description 4
- 239000007787 solid Substances 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- 230000008901 benefit Effects 0.000 description 3
- 238000004040 coloring Methods 0.000 description 3
- 239000004205 dimethyl polysiloxane Substances 0.000 description 3
- 230000035784 germination Effects 0.000 description 3
- 239000000314 lubricant Substances 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 150000003961 organosilicon compounds Chemical class 0.000 description 3
- 230000000361 pesticidal effect Effects 0.000 description 3
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 description 3
- UFNOUKDBUJZYDE-UHFFFAOYSA-N 2-(4-chlorophenyl)-3-cyclopropyl-1-(1H-1,2,4-triazol-1-yl)butan-2-ol Chemical compound C1=NC=NN1CC(O)(C=1C=CC(Cl)=CC=1)C(C)C1CC1 UFNOUKDBUJZYDE-UHFFFAOYSA-N 0.000 description 2
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- 239000003086 colorant Substances 0.000 description 2
- 238000000151 deposition Methods 0.000 description 2
- 239000000428 dust Substances 0.000 description 2
- 210000002257 embryonic structure Anatomy 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 230000000442 meristematic effect Effects 0.000 description 2
- 239000000575 pesticide Substances 0.000 description 2
- BAZVSMNPJJMILC-UHFFFAOYSA-N triadimenol Chemical compound C1=NC=NN1C(C(O)C(C)(C)C)OC1=CC=C(Cl)C=C1 BAZVSMNPJJMILC-UHFFFAOYSA-N 0.000 description 2
- PITWUHDDNUVBPT-UHFFFAOYSA-N Cloethocarb Chemical compound CNC(=O)OC1=CC=CC=C1OC(CCl)OC PITWUHDDNUVBPT-UHFFFAOYSA-N 0.000 description 1
- 239000005757 Cyproconazole Substances 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- 239000005769 Etridiazole Substances 0.000 description 1
- 241000201976 Polycarpon Species 0.000 description 1
- 239000005843 Thiram Substances 0.000 description 1
- 239000005846 Triadimenol Substances 0.000 description 1
- 241000607479 Yersinia pestis Species 0.000 description 1
- 239000002671 adjuvant Substances 0.000 description 1
- 125000002877 alkyl aryl group Chemical group 0.000 description 1
- 230000000843 anti-fungal effect Effects 0.000 description 1
- 229940121375 antifungal agent Drugs 0.000 description 1
- 125000003710 aryl alkyl group Chemical group 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 125000000753 cycloalkyl group Chemical group 0.000 description 1
- 125000002704 decyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 230000008021 deposition Effects 0.000 description 1
- 201000010099 disease Diseases 0.000 description 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 1
- 238000010410 dusting Methods 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 125000003187 heptyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000012669 liquid formulation Substances 0.000 description 1
- 125000001421 myristyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000001400 nonyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 125000000913 palmityl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 125000002958 pentadecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 230000008635 plant growth Effects 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000004447 silicone coating Substances 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000004546 suspension concentrate Substances 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 239000004308 thiabendazole Substances 0.000 description 1
- 229960004546 thiabendazole Drugs 0.000 description 1
- 235000010296 thiabendazole Nutrition 0.000 description 1
- 125000002948 undecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 230000035899 viability Effects 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01C—PLANTING; SOWING; FERTILISING
- A01C1/00—Apparatus, or methods of use thereof, for testing or treating seed, roots, or the like, prior to sowing or planting
- A01C1/06—Coating or dressing seed
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Soil Sciences (AREA)
- Environmental Sciences (AREA)
- Pretreatment Of Seeds And Plants (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US09/769,388 US7081436B2 (en) | 2001-01-26 | 2001-01-26 | Paste formulation for seed treatment of plants |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ZA200304946B true ZA200304946B (en) | 2004-07-28 |
Family
ID=25085292
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ZA200304946A ZA200304946B (en) | 2001-01-26 | 2003-06-25 | Paste formulation for seed treatment of plants. |
Country Status (12)
| Country | Link |
|---|---|
| US (1) | US7081436B2 (es) |
| EP (1) | EP1353543A1 (es) |
| KR (1) | KR20040011457A (es) |
| CN (1) | CN1489436A (es) |
| AU (1) | AU2002241920A1 (es) |
| BR (1) | BR0206660A (es) |
| CA (1) | CA2434225A1 (es) |
| IL (1) | IL156663A0 (es) |
| MX (1) | MXPA03006626A (es) |
| NZ (1) | NZ527049A (es) |
| WO (1) | WO2002058454A1 (es) |
| ZA (1) | ZA200304946B (es) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA2355812A1 (en) * | 2001-08-24 | 2003-02-24 | George Lazarovits | Method for control of bacterial spot |
| GB0312195D0 (en) * | 2003-05-28 | 2003-07-02 | Syngenta Ltd | Formulation |
| GB0508993D0 (en) | 2005-05-03 | 2005-06-08 | Syngenta Participations Ag | Pesticidal compositions |
| US8209902B2 (en) * | 2009-07-02 | 2012-07-03 | Nanotech Industries, Inc. | Biologically active multifunctional nanochips and method of application thereof for production of high-quality seed |
| US8557504B2 (en) * | 2010-06-18 | 2013-10-15 | Eastman Kodak Company | Thermally ablatable lithographic printing plate precursors |
| BR112021022144A2 (pt) | 2019-05-08 | 2021-12-28 | Evonik Operations Gmbh | Siloxanos modificados com poliéter como aglutinantes de pó para semente |
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|---|---|---|---|---|
| GB1141796A (es) | 1900-01-01 | |||
| GB1141798A (en) | 1965-05-26 | 1969-01-29 | Birfield Eng Ltd | Improvements in or relating to universal joints |
| US4182716A (en) | 1978-09-05 | 1980-01-08 | Uniroyal, Ltd. | Method of making 5,6-dihydro-2-methyl-N-phenyl-1,4-oxathiin-3-carboxamide |
| FR2498201A2 (fr) * | 1980-06-11 | 1982-07-23 | Roussel Uclaf | Compositions stables a la lumiere contenant des composes pyrethrinoides et des colorants |
| CA1150284A (en) | 1980-12-02 | 1983-07-19 | Allan K.S. Tsai | Method of making certain 2,3-dihydro-1,4-dithiins |
| UST101902I4 (en) | 1981-03-25 | 1982-06-01 | Pesticidal composition and method for treating seeds prior to planting | |
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| JPS5939808A (ja) | 1982-08-31 | 1984-03-05 | Shin Etsu Chem Co Ltd | 衛生・農業害虫駆除剤 |
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| US5176735A (en) | 1990-06-28 | 1993-01-05 | Uniroyal Chemical Company, Inc. | Method of desiccating plants employing 3-carbonylphenyl uracil derivatives |
| US5061716A (en) | 1990-09-13 | 1991-10-29 | Uniroyal Chemical Company, Inc. | Fungicidal 3,3-bisthioalkyl-2-pyridylacrylic acid compounds |
| US5114464A (en) | 1990-09-27 | 1992-05-19 | Uniroyal Chemical Company, Inc. | 4-quinoxalinyloxyphenoxyalkylinitrile herbicides |
| US5070211A (en) | 1990-10-01 | 1991-12-03 | Uniroyal Chemical Company, Inc. | Dioxo heterocyclic compounds, composition containing same and process for plant growth regulation using same |
| US5071862A (en) | 1990-10-26 | 1991-12-10 | Uniroyal Chemical Company, Inc. | 2-(3-oxypyridinyl)-1,3-dioxolane and dioxane compounds, compositions containing same and process for controlling fungi using same |
| ATE131851T1 (de) | 1991-07-19 | 1996-01-15 | Uniroyal Chem Co Inc | Zusammensetzungen zur verwendung von filmen auf saatgut |
| US5169430A (en) | 1991-08-09 | 1992-12-08 | Uniroyal Chemical Company, Inc. | Benzenesulfonamide derivatives and methods for their production |
| US5134133A (en) | 1991-09-30 | 1992-07-28 | Uniroyal Chemical Company, Inc. | Oxime phosphate pesticidal compounds, compositions and methods |
| US5215747A (en) | 1992-02-07 | 1993-06-01 | Uniroyal Chemical Company, Inc. | Composition and method for protecting plants from phytopathogenic fungi |
| US5558806A (en) * | 1992-07-23 | 1996-09-24 | Osi Specialties, Inc. | Surfactant blend of a polyalkleneoxide polysiloxane and an organic compound having a short chain hydrophobic moiety |
| US5580544A (en) | 1995-03-29 | 1996-12-03 | Uniroyal Chemical Company, Inc. | Paste formulation useful for seed treatment and foliar treatment of plants |
| RU2104626C1 (ru) * | 1996-09-30 | 1998-02-20 | Открытое акционерное общество "Химпром" | Состав для обработки семян |
-
2001
- 2001-01-26 US US09/769,388 patent/US7081436B2/en not_active Expired - Lifetime
-
2002
- 2002-01-22 KR KR20037009771A patent/KR20040011457A/ko not_active Application Discontinuation
- 2002-01-22 IL IL15666302A patent/IL156663A0/xx unknown
- 2002-01-22 CN CNA028041445A patent/CN1489436A/zh active Pending
- 2002-01-22 AU AU2002241920A patent/AU2002241920A1/en not_active Abandoned
- 2002-01-22 BR BR0206660-2A patent/BR0206660A/pt not_active IP Right Cessation
- 2002-01-22 EP EP02707517A patent/EP1353543A1/en not_active Withdrawn
- 2002-01-22 NZ NZ527049A patent/NZ527049A/en unknown
- 2002-01-22 WO PCT/US2002/001437 patent/WO2002058454A1/en not_active Application Discontinuation
- 2002-01-22 MX MXPA03006626A patent/MXPA03006626A/es unknown
- 2002-01-22 CA CA002434225A patent/CA2434225A1/en not_active Abandoned
-
2003
- 2003-06-25 ZA ZA200304946A patent/ZA200304946B/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| CA2434225A1 (en) | 2002-08-01 |
| KR20040011457A (ko) | 2004-02-05 |
| IL156663A0 (en) | 2004-01-04 |
| US20020147111A1 (en) | 2002-10-10 |
| MXPA03006626A (es) | 2003-10-15 |
| US7081436B2 (en) | 2006-07-25 |
| AU2002241920A1 (en) | 2002-08-06 |
| NZ527049A (en) | 2005-02-25 |
| WO2002058454A1 (en) | 2002-08-01 |
| BR0206660A (pt) | 2004-06-22 |
| CN1489436A (zh) | 2004-04-14 |
| EP1353543A1 (en) | 2003-10-22 |
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