UA79571C2 - Metod for the protection of seeds from soil pests comprising - Google Patents

Metod for the protection of seeds from soil pests comprising Download PDF

Info

Publication number: UA79571C2
Authority: UA; Ukraine
Prior art keywords: formula; seeds; compound; compounds; alkyl
Prior art date: 2003-12-04

Application number

UAA200607447A

Other languages

English (en)

Ukrainian (uk)

Inventor

Dein Wolfgang Von

Hassan Oloumi-Sadeghi

David G Kuhn

Nigel Armes

Henry Van Cotter

Carol Hicks

Original Assignee

Basf Ag

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.)

2003-12-04

Filing date

2004-02-12

Publication date

2007-06-25

2004-02-12 Application filed by Basf Ag filed Critical Basf Ag

2007-06-25 Publication of UA79571C2 publication Critical patent/UA79571C2/uk

Links

241000607479 Yersinia pestis Species 0.000 title claims abstract description 21
239000002689 soil Substances 0.000 title claims abstract description 15
150000001875 compounds Chemical class 0.000 claims abstract description 70
238000000034 method Methods 0.000 claims abstract description 15
239000000460 chlorine Substances 0.000 claims abstract description 10
229910052801 chlorine Inorganic materials 0.000 claims abstract description 10
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims abstract description 9
125000005843 halogen group Chemical group 0.000 claims abstract description 9
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims abstract description 6
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims abstract description 6
229910052794 bromium Inorganic materials 0.000 claims abstract description 6
238000009331 sowing Methods 0.000 claims abstract description 6
125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims abstract description 5
HBAQYPYDRFILMT-UHFFFAOYSA-N 8-[3-(1-cyclopropylpyrazol-4-yl)-1H-pyrazolo[4,3-d]pyrimidin-5-yl]-3-methyl-3,8-diazabicyclo[3.2.1]octan-2-one Chemical class C1(CC1)N1N=CC(=C1)C1=NNC2=C1N=C(N=C2)N1C2C(N(CC1CC2)C)=O HBAQYPYDRFILMT-UHFFFAOYSA-N 0.000 claims abstract description 4
150000003839 salts Chemical class 0.000 claims abstract description 4
239000001257 hydrogen Substances 0.000 claims abstract description 3
229910052739 hydrogen Inorganic materials 0.000 claims abstract description 3
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 3
230000035784 germination Effects 0.000 claims description 3
238000012876 topography Methods 0.000 claims 1
125000000217 alkyl group Chemical group 0.000 abstract description 7
125000000753 cycloalkyl group Chemical group 0.000 abstract description 3
125000003545 alkoxy group Chemical group 0.000 abstract description 2
125000001309 chloro group Chemical group Cl* 0.000 abstract description 2
125000003342 alkenyl group Chemical group 0.000 abstract 1
125000000304 alkynyl group Chemical group 0.000 abstract 1
125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 1
-1 1-methylpentyl Chemical group 0.000 description 32
239000000203 mixture Substances 0.000 description 23
239000013543 active substance Substances 0.000 description 20
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 20
239000000839 emulsion Substances 0.000 description 11
239000008187 granular material Substances 0.000 description 11
239000000843 powder Substances 0.000 description 11
239000000126 substance Substances 0.000 description 10
239000002270 dispersing agent Substances 0.000 description 9
239000006185 dispersion Substances 0.000 description 9
230000000694 effects Effects 0.000 description 9
239000003921 oil Substances 0.000 description 9
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 8
238000011282 treatment Methods 0.000 description 8
239000000080 wetting agent Substances 0.000 description 8
239000000945 filler Substances 0.000 description 7
241000196324 Embryophyta Species 0.000 description 6
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 6
235000002017 Zea mays subsp mays Nutrition 0.000 description 6
235000005822 corn Nutrition 0.000 description 6
JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 6
239000000243 solution Substances 0.000 description 6
239000002904 solvent Substances 0.000 description 6
238000005507 spraying Methods 0.000 description 6
239000000725 suspension Substances 0.000 description 6
240000008042 Zea mays Species 0.000 description 5
239000000853 adhesive Substances 0.000 description 5
239000003995 emulsifying agent Substances 0.000 description 5
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 5
239000006072 paste Substances 0.000 description 5
239000007787 solid Substances 0.000 description 5
241001136249 Agriotes lineatus Species 0.000 description 4
LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 4
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 4
239000002253 acid Substances 0.000 description 4
230000001070 adhesive effect Effects 0.000 description 4
235000013339 cereals Nutrition 0.000 description 4
125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 description 4
235000014113 dietary fatty acids Nutrition 0.000 description 4
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 4
239000000194 fatty acid Substances 0.000 description 4
229930195729 fatty acid Natural products 0.000 description 4
150000004665 fatty acids Chemical class 0.000 description 4
235000013312 flour Nutrition 0.000 description 4
239000000463 material Substances 0.000 description 4
239000000575 pesticide Substances 0.000 description 4
239000000047 product Substances 0.000 description 4
125000001424 substituent group Chemical group 0.000 description 4
239000008096 xylene Substances 0.000 description 4
125000004169 (C1-C6) alkyl group Chemical group 0.000 description 3
WVDDGKGOMKODPV-UHFFFAOYSA-N Benzyl alcohol Chemical compound OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 description 3
241000254173 Coleoptera Species 0.000 description 3
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
240000007594 Oryza sativa Species 0.000 description 3
235000007164 Oryza sativa Nutrition 0.000 description 3
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
235000012211 aluminium silicate Nutrition 0.000 description 3
JFDZBHWFFUWGJE-UHFFFAOYSA-N benzonitrile Chemical compound N#CC1=CC=CC=C1 JFDZBHWFFUWGJE-UHFFFAOYSA-N 0.000 description 3
239000004359 castor oil Substances 0.000 description 3
235000019438 castor oil Nutrition 0.000 description 3
239000003795 chemical substances by application Substances 0.000 description 3
150000002191 fatty alcohols Chemical class 0.000 description 3
NYPJDWWKZLNGGM-UHFFFAOYSA-N fenvalerate Aalpha Natural products C=1C=C(Cl)C=CC=1C(C(C)C)C(=O)OC(C#N)C(C=1)=CC=CC=1OC1=CC=CC=C1 NYPJDWWKZLNGGM-UHFFFAOYSA-N 0.000 description 3
ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 3
150000007857 hydrazones Chemical class 0.000 description 3
229910052740 iodine Inorganic materials 0.000 description 3
238000002360 preparation method Methods 0.000 description 3
235000009566 rice Nutrition 0.000 description 3
241000894007 species Species 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
239000005995 Aluminium silicate Substances 0.000 description 2
241000238421 Arthropoda Species 0.000 description 2
235000014698 Brassica juncea var multisecta Nutrition 0.000 description 2
235000006008 Brassica napus var napus Nutrition 0.000 description 2
240000000385 Brassica napus var. napus Species 0.000 description 2
235000006618 Brassica rapa subsp oleifera Nutrition 0.000 description 2
235000004977 Brassica sinapistrum Nutrition 0.000 description 2
229920000742 Cotton Polymers 0.000 description 2
IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 2
239000005898 Fenoxycarb Substances 0.000 description 2
VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 2
244000299507 Gossypium hirsutum Species 0.000 description 2
244000020551 Helianthus annuus Species 0.000 description 2
235000003222 Helianthus annuus Nutrition 0.000 description 2
241000238631 Hexapoda Species 0.000 description 2
240000005979 Hordeum vulgare Species 0.000 description 2
235000007340 Hordeum vulgare Nutrition 0.000 description 2
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
239000005907 Indoxacarb Substances 0.000 description 2
CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 2
AFVFQIVMOAPDHO-UHFFFAOYSA-N Methanesulfonic acid Chemical compound CS(O)(=O)=O AFVFQIVMOAPDHO-UHFFFAOYSA-N 0.000 description 2
AMQJEAYHLZJPGS-UHFFFAOYSA-N N-Pentanol Chemical compound CCCCCO AMQJEAYHLZJPGS-UHFFFAOYSA-N 0.000 description 2
UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 2
229920003171 Poly (ethylene oxide) Polymers 0.000 description 2
229920002873 Polyethylenimine Polymers 0.000 description 2
LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical compound OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 description 2
239000004480 active ingredient Substances 0.000 description 2
150000001298 alcohols Chemical class 0.000 description 2
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150000008052 alkyl sulfonates Chemical class 0.000 description 2
150000001411 amidrazones Chemical class 0.000 description 2
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230000015572 biosynthetic process Effects 0.000 description 2
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HJOVHMDZYOCNQW-UHFFFAOYSA-N isophorone Chemical compound CC1=CC(=O)CC(C)(C)C1 HJOVHMDZYOCNQW-UHFFFAOYSA-N 0.000 description 2
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 2
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HOKKPVIRMVDYPB-UVTDQMKNSA-N (Z)-thiacloprid Chemical compound C1=NC(Cl)=CC=C1CN1C(=N/C#N)/SCC1 HOKKPVIRMVDYPB-UVTDQMKNSA-N 0.000 description 1
ATROHALUCMTWTB-WYMLVPIESA-N (z)-n-diethoxyphosphinothioyloxybenzenecarboximidoyl cyanide Chemical compound CCOP(=S)(OCC)O\N=C(/C#N)C1=CC=CC=C1 ATROHALUCMTWTB-WYMLVPIESA-N 0.000 description 1
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NFGXHKASABOEEW-UHFFFAOYSA-N 1-methylethyl 11-methoxy-3,7,11-trimethyl-2,4-dodecadienoate Chemical compound COC(C)(C)CCCC(C)CC=CC(C)=CC(=O)OC(C)C NFGXHKASABOEEW-UHFFFAOYSA-N 0.000 description 1
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229910052731 fluorine Inorganic materials 0.000 description 1
239000011737 fluorine Substances 0.000 description 1
RMFNNCGOSPBBAD-MDWZMJQESA-N formetanate Chemical compound CNC(=O)OC1=CC=CC(\N=C\N(C)C)=C1 RMFNNCGOSPBBAD-MDWZMJQESA-N 0.000 description 1
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239000000417 fungicide Substances 0.000 description 1
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230000002335 preservative effect Effects 0.000 description 1
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QYMMJNLHFKGANY-UHFFFAOYSA-N profenofos Chemical compound CCCSP(=O)(OCC)OC1=CC=C(Br)C=C1Cl QYMMJNLHFKGANY-UHFFFAOYSA-N 0.000 description 1
BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
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DWFZBUWUXWZWKD-UHFFFAOYSA-N pyridaben Chemical compound C1=CC(C(C)(C)C)=CC=C1CSC1=C(Cl)C(=O)N(C(C)(C)C)N=C1 DWFZBUWUXWZWKD-UHFFFAOYSA-N 0.000 description 1
NHDHVHZZCFYRSB-UHFFFAOYSA-N pyriproxyfen Chemical compound C=1C=CC=NC=1OC(C)COC(C=C1)=CC=C1OC1=CC=CC=C1 NHDHVHZZCFYRSB-UHFFFAOYSA-N 0.000 description 1
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125000003548 sec-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
HPYNBECUCCGGPA-UHFFFAOYSA-N silafluofen Chemical compound C1=CC(OCC)=CC=C1[Si](C)(C)CCCC1=CC=C(F)C(OC=2C=CC=CC=2)=C1 HPYNBECUCCGGPA-UHFFFAOYSA-N 0.000 description 1
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DTDSAWVUFPGDMX-UHFFFAOYSA-N spirodiclofen Chemical compound CCC(C)(C)C(=O)OC1=C(C=2C(=CC(Cl)=CC=2)Cl)C(=O)OC11CCCCC1 DTDSAWVUFPGDMX-UHFFFAOYSA-N 0.000 description 1
239000007921 spray Substances 0.000 description 1
238000001694 spray drying Methods 0.000 description 1
239000001384 succinic acid Substances 0.000 description 1
150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
JXHJNEJVUNHLKO-UHFFFAOYSA-N sulprofos Chemical compound CCCSP(=S)(OCC)OC1=CC=C(SC)C=C1 JXHJNEJVUNHLKO-UHFFFAOYSA-N 0.000 description 1
238000003786 synthesis reaction Methods 0.000 description 1
239000005936 tau-Fluvalinate Substances 0.000 description 1
INISTDXBRIBGOC-XMMISQBUSA-N tau-fluvalinate Chemical compound N([C@H](C(C)C)C(=O)OC(C#N)C=1C=C(OC=2C=CC=CC=2)C=CC=1)C1=CC=C(C(F)(F)F)C=C1Cl INISTDXBRIBGOC-XMMISQBUSA-N 0.000 description 1
QYPNKSZPJQQLRK-UHFFFAOYSA-N tebufenozide Chemical compound C1=CC(CC)=CC=C1C(=O)NN(C(C)(C)C)C(=O)C1=CC(C)=CC(C)=C1 QYPNKSZPJQQLRK-UHFFFAOYSA-N 0.000 description 1
ZZYSLNWGKKDOML-UHFFFAOYSA-N tebufenpyrad Chemical compound CCC1=NN(C)C(C(=O)NCC=2C=CC(=CC=2)C(C)(C)C)=C1Cl ZZYSLNWGKKDOML-UHFFFAOYSA-N 0.000 description 1
CJDWRQLODFKPEL-UHFFFAOYSA-N teflubenzuron Chemical compound FC1=CC=CC(F)=C1C(=O)NC(=O)NC1=CC(Cl)=C(F)C(Cl)=C1F CJDWRQLODFKPEL-UHFFFAOYSA-N 0.000 description 1
125000001973 tert-pentyl group Chemical group [H]C([H])([H])C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
CXWXQJXEFPUFDZ-UHFFFAOYSA-N tetralin Chemical compound C1=CC=C2CCCCC2=C1 CXWXQJXEFPUFDZ-UHFFFAOYSA-N 0.000 description 1
NWWZPOKUUAIXIW-FLIBITNWSA-N thiamethoxam Chemical compound [O-][N+](=O)\N=C/1N(C)COCN\1CC1=CN=C(Cl)S1 NWWZPOKUUAIXIW-FLIBITNWSA-N 0.000 description 1
239000002562 thickening agent Substances 0.000 description 1
DNVLJEWNNDHELH-UHFFFAOYSA-N thiocyclam Chemical compound CN(C)C1CSSSC1 DNVLJEWNNDHELH-UHFFFAOYSA-N 0.000 description 1
BAKXBZPQTXCKRR-UHFFFAOYSA-N thiodicarb Chemical compound CSC(C)=NOC(=O)NSNC(=O)ON=C(C)SC BAKXBZPQTXCKRR-UHFFFAOYSA-N 0.000 description 1
231100000331 toxic Toxicity 0.000 description 1
230000002588 toxic effect Effects 0.000 description 1
NKNFWVNSBIXGLL-UHFFFAOYSA-N triazamate Chemical compound CCOC(=O)CSC1=NC(C(C)(C)C)=NN1C(=O)N(C)C NKNFWVNSBIXGLL-UHFFFAOYSA-N 0.000 description 1
AMFGTOFWMRQMEM-UHFFFAOYSA-N triazophos Chemical compound N1=C(OP(=S)(OCC)OCC)N=CN1C1=CC=CC=C1 AMFGTOFWMRQMEM-UHFFFAOYSA-N 0.000 description 1
NFACJZMKEDPNKN-UHFFFAOYSA-N trichlorfon Chemical compound COP(=O)(OC)C(O)C(Cl)(Cl)Cl NFACJZMKEDPNKN-UHFFFAOYSA-N 0.000 description 1
XAIPTRIXGHTTNT-UHFFFAOYSA-N triflumuron Chemical compound C1=CC(OC(F)(F)F)=CC=C1NC(=O)NC(=O)C1=CC=CC=C1Cl XAIPTRIXGHTTNT-UHFFFAOYSA-N 0.000 description 1
238000009827 uniform distribution Methods 0.000 description 1
150000003672 ureas Chemical class 0.000 description 1
NQPDZGIKBAWPEJ-UHFFFAOYSA-N valeric acid Chemical compound CCCCC(O)=O NQPDZGIKBAWPEJ-UHFFFAOYSA-N 0.000 description 1
235000013311 vegetables Nutrition 0.000 description 1
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238000009736 wetting Methods 0.000 description 1
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239000005943 zeta-Cypermethrin 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
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/52—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing groups, e.g. carboxylic acid amidines
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P33/00—Antiparasitic agents

Landscapes

Life Sciences & Earth Sciences (AREA)
Health & Medical Sciences (AREA)
General Health & Medical Sciences (AREA)
Environmental Sciences (AREA)
Zoology (AREA)
Wood Science & Technology (AREA)
Dentistry (AREA)
Engineering & Computer Science (AREA)
Plant Pathology (AREA)
Pest Control & Pesticides (AREA)
Agronomy & Crop Science (AREA)
Veterinary Medicine (AREA)
Chemical & Material Sciences (AREA)
Tropical Medicine & Parasitology (AREA)
Animal Behavior & Ethology (AREA)
Chemical Kinetics & Catalysis (AREA)
Pharmacology & Pharmacy (AREA)
Organic Chemistry (AREA)
Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
Medicinal Chemistry (AREA)
General Chemical & Material Sciences (AREA)
Public Health (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Pretreatment Of Seeds And Plants (AREA)
Plural Heterocyclic Compounds (AREA)
Pyridine Compounds (AREA)
Catching Or Destruction (AREA)
Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)

UAA200607447A 2003-12-04 2004-02-12 Metod for the protection of seeds from soil pests comprising UA79571C2 (en)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
US52660903P	2003-12-04	2003-12-04
PCT/EP2004/013686 WO2005053401A2 (en)	2003-12-04	2004-12-02	N-arylhydrazine derivatives for seed treatment

Publications (1)

Publication Number	Publication Date
UA79571C2 true UA79571C2 (en)	2007-06-25

Family

ID=34652460

Family Applications (2)

Application Number	Title	Priority Date	Filing Date
UAA200607447A UA79571C2 (en)	2003-12-04	2004-02-12	Metod for the protection of seeds from soil pests comprising
UAA200607448A UA81561C2 (en)	2003-12-04	2004-12-02	Use of n-arylhydrazine derivative and method for controlling non-crop pests

Family Applications After (1)

Application Number	Title	Priority Date	Filing Date
UAA200607448A UA81561C2 (en)	2003-12-04	2004-12-02	Use of n-arylhydrazine derivative and method for controlling non-crop pests

Country Status (34)

Country	Link
US (2)	US20070259962A1 (de)
EP (3)	EP1691607B1 (de)
JP (3)	JP2007513117A (de)
KR (3)	KR20060123241A (de)
CN (3)	CN1889833A (de)
AP (1)	AP1959A (de)
AR (2)	AR046745A1 (de)
AT (3)	ATE359707T1 (de)
AU (3)	AU2004294298A1 (de)
BR (3)	BRPI0417247A (de)
CA (3)	CA2546110A1 (de)
CO (2)	CO5680375A2 (de)
CR (1)	CR8451A (de)
DE (3)	DE602004006020T2 (de)
DK (2)	DK1694122T3 (de)
EA (3)	EA200601077A1 (de)
EC (2)	ECSP066609A (de)
ES (2)	ES2290785T3 (de)
IL (3)	IL175544A0 (de)
MA (2)	MA28280A1 (de)
MX (1)	MXPA06005988A (de)
MY (1)	MY137761A (de)
NO (1)	NO20062632L (de)
NZ (1)	NZ547362A (de)
OA (1)	OA13292A (de)
PE (1)	PE20050702A1 (de)
PL (2)	PL1691607T3 (de)
PT (1)	PT1691607E (de)
SI (2)	SI1691607T1 (de)
TW (3)	TW200528022A (de)
UA (2)	UA79571C2 (de)
UY (2)	UY28654A1 (de)
WO (3)	WO2005053402A2 (de)
ZA (3)	ZA200605458B (de)

Families Citing this family (23)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
WO2006128865A1 (en) *	2005-06-03	2006-12-07	Basf Aktiengesellschaft	Method of combating bugs
MX2007015020A (es) *	2005-06-03	2008-01-17	Basf Ag	Composicion para la impregnacion de fibras, telas y mallas que comparte una actividad protectora contra plagas.
WO2007051756A1 (en) *	2005-11-04	2007-05-10	Basf Se	Crystalline modification of n-ethyl-2,2-dichloro-1-methylcyclopropane-carboxamide-2-(2,6-dichloro- alpha,alpha,alpha -trifluoro-p-tolyl)hydrazone
JP5239148B2 (ja) *	2005-12-01	2013-07-17	住友化学株式会社	３−イミノプロペン化合物、それを含有する有害生物防除剤、およびその有害生物防除用途
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2004
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2006
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Also Published As

Publication number	Publication date
EP1691607A2 (de)	2006-08-23
CO5670341A2 (es)	2006-08-31
SI1694122T1 (sl)	2007-12-31
TW200529750A (en)	2005-09-16
BRPI0417060A (pt)	2007-03-27
BRPI0417247A (pt)	2007-03-06
PL1691607T3 (pl)	2007-09-28
ZA200605458B (en)	2007-11-28
JP2007513117A (ja)	2007-05-24
BRPI0417181A (pt)	2007-03-06
US20070259962A1 (en)	2007-11-08
OA13292A (en)	2007-01-31
DE602004008966T2 (de)	2008-01-17
CO5680375A2 (es)	2006-09-29
ES2290785T3 (es)	2008-02-16
UY28655A1 (es)	2005-06-30
IL175544A0 (en)	2006-09-05
WO2005053401A3 (en)	2005-07-28
ZA200605459B (en)	2007-11-28
CR8451A (es)	2006-12-07
ZA200605460B (en)	2007-12-27
CA2547412A1 (en)	2005-06-16
NO20062632L (no)	2006-06-27
TW200528022A (en)	2005-09-01
IL175852A0 (en)	2006-10-05
WO2005053403A2 (en)	2005-06-16
MA28282A1 (fr)	2006-11-01
PL1694122T3 (pl)	2008-01-31
EP1694122A2 (de)	2006-08-30
AU2004294712A1 (en)	2005-06-16
ECSP066609A (es)	2006-10-25
DK1691607T3 (da)	2007-07-30
ES2285550T3 (es)	2007-11-16
AR046745A1 (es)	2005-12-21
AP2006003647A0 (en)	2006-06-30
CA2546110A1 (en)	2005-06-16
EP1694122B1 (de)	2007-09-12
ATE359707T1 (de)	2007-05-15
US20070129442A1 (en)	2007-06-07
CN1889834A (zh)	2007-01-03
AU2004294712B2 (en)	2010-04-22
CN1889832A (zh)	2007-01-03
AR046746A1 (es)	2005-12-21
MY137761A (en)	2009-03-31
UY28654A1 (es)	2005-06-30
DE602004019995D1 (de)	2009-04-23
KR20060115889A (ko)	2006-11-10
CA2547420A1 (en)	2005-06-16
DK1694122T3 (da)	2007-12-03
KR20060123241A (ko)	2006-12-01
DE602004008966D1 (de)	2007-10-25
TW200529836A (en)	2005-09-16
PT1691607E (pt)	2007-05-31
IL175712A0 (en)	2006-09-05
DE602004006020D1 (de)	2007-05-31
EP1841317B1 (de)	2009-03-11
EA200601076A1 (ru)	2006-10-27
DE602004006020T2 (de)	2007-08-23
AU2004294299A1 (en)	2005-06-16
JP2007513116A (ja)	2007-05-24
ATE372674T1 (de)	2007-09-15
KR20060123420A (ko)	2006-12-01
WO2005053402A2 (en)	2005-06-16
MXPA06005988A (es)	2006-08-23
WO2005053403A3 (en)	2005-07-28
JP2007513115A (ja)	2007-05-24
CN100438760C (zh)	2008-12-03
WO2005053402A3 (en)	2005-08-04
ATE424724T1 (de)	2009-03-15
PE20050702A1 (es)	2005-10-24
NZ547362A (en)	2008-12-24
SI1691607T1 (sl)	2007-10-31
EA200601078A1 (ru)	2006-10-27
EP1841317A2 (de)	2007-10-10
ECSP066632A (es)	2006-10-25
WO2005053401A2 (en)	2005-06-16
TWI304724B (en)	2009-01-01
AU2004294298A1 (en)	2005-06-16
AP1959A (en)	2009-02-20
MA28280A1 (fr)	2006-11-01
CN1889833A (zh)	2007-01-03
EA200601077A1 (ru)	2006-10-27
UA81561C2 (en)	2008-01-10
EP1691607B1 (de)	2007-04-18
EA010019B1 (ru)	2008-06-30

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