BR9917869B1

BR9917869B1 - processo e aplicação de fipronil para o combate de organismos daninhos em plantas de algodão alteradas geneticamente.

processo e aplicação de fipronil para o combate de organismos daninhos em plantas de algodão alteradas geneticamente. Download PDF

Info

Publication number: BR9917869B1
Authority: BR; Brazil
Prior art keywords: group; radicals; alkyl; process according; original document
Prior art date: 1998-06-05

Application number

BRPI9917869-9A

Other languages

English (en)

Portuguese (pt)

Inventor

Manfred Kern

Priority date

1998-06-05

Filing date

1999-06-01

Publication date

2012-09-18

1999-06-01 Application filed filed Critical

2012-09-18 Publication of BR9917869B1 publication Critical patent/BR9917869B1/pt

Links

241000196324 Embryophyta Species 0.000 title claims description 39
238000000034 method Methods 0.000 title claims description 31
230000008569 process Effects 0.000 title claims description 25
240000002024 Gossypium herbaceum Species 0.000 title claims description 20
235000004341 Gossypium herbaceum Nutrition 0.000 title claims description 20
ZOCSXAVNDGMNBV-UHFFFAOYSA-N 5-amino-1-[2,6-dichloro-4-(trifluoromethyl)phenyl]-4-[(trifluoromethyl)sulfinyl]-1H-pyrazole-3-carbonitrile Chemical compound NC1=C(S(=O)C(F)(F)F)C(C#N)=NN1C1=C(Cl)C=C(C(F)(F)F)C=C1Cl ZOCSXAVNDGMNBV-UHFFFAOYSA-N 0.000 title claims description 15
239000005899 Fipronil Substances 0.000 title claims description 10
229940013764 fipronil Drugs 0.000 title claims description 10
239000000203 mixture Substances 0.000 claims description 31
150000001875 compounds Chemical class 0.000 claims description 20
238000009472 formulation Methods 0.000 claims description 20
108090000623 proteins and genes Proteins 0.000 claims description 20
239000002917 insecticide Substances 0.000 claims description 17
241000193388 Bacillus thuringiensis Species 0.000 claims description 15
229940097012 bacillus thuringiensis Drugs 0.000 claims description 15
230000000749 insecticidal effect Effects 0.000 claims description 15
102000004169 proteins and genes Human genes 0.000 claims description 10
241000238631 Hexapoda Species 0.000 claims description 8
239000000463 material Substances 0.000 claims description 6
241000255777 Lepidoptera Species 0.000 claims description 5
IAJOBQBIJHVGMQ-UHFFFAOYSA-N 2-amino-4-[hydroxy(methyl)phosphoryl]butanoic acid Chemical compound CP(O)(=O)CCC(N)C(O)=O IAJOBQBIJHVGMQ-UHFFFAOYSA-N 0.000 claims description 4
239000005561 Glufosinate Substances 0.000 claims description 4
239000005562 Glyphosate Substances 0.000 claims description 4
241000258937 Hemiptera Species 0.000 claims description 4
229940097068 glyphosate Drugs 0.000 claims description 4
XDDAORKBJWWYJS-UHFFFAOYSA-N glyphosate Chemical compound OC(=O)CNCP(O)(O)=O XDDAORKBJWWYJS-UHFFFAOYSA-N 0.000 claims description 4
241000254173 Coleoptera Species 0.000 claims description 3
230000000855 fungicidal effect Effects 0.000 claims description 3
230000002363 herbicidal effect Effects 0.000 claims description 2
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239000013543 active substance Substances 0.000 description 26
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230000014509 gene expression Effects 0.000 description 14
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IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 12
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OWZREIFADZCYQD-UHFFFAOYSA-N [cyano-(3-phenoxyphenyl)methyl] 3-(2,2-dibromoethenyl)-2,2-dimethylcyclopropane-1-carboxylate Chemical compound CC1(C)C(C=C(Br)Br)C1C(=O)OC(C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 OWZREIFADZCYQD-UHFFFAOYSA-N 0.000 description 10
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229910052739 hydrogen Inorganic materials 0.000 description 9
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238000002360 preparation method Methods 0.000 description 8
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QXAITBQSYVNQDR-ZIOPAAQOSA-N amitraz Chemical compound C=1C=C(C)C=C(C)C=1/N=C/N(C)\C=N\C1=CC=C(C)C=C1C QXAITBQSYVNQDR-ZIOPAAQOSA-N 0.000 description 5
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125000005843 halogen group Chemical group 0.000 description 5
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239000000243 solution Substances 0.000 description 5
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125000000008 (C1-C10) alkyl group Chemical group 0.000 description 4
125000000171 (C1-C6) haloalkyl group Chemical group 0.000 description 4
125000006528 (C2-C6) alkyl group Chemical group 0.000 description 4
125000006564 (C4-C8) cycloalkyl group Chemical group 0.000 description 4
241000218475 Agrotis segetum Species 0.000 description 4
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 4
FIPWRIJSWJWJAI-UHFFFAOYSA-N Butyl carbitol 6-propylpiperonyl ether Chemical compound C1=C(CCC)C(COCCOCCOCCCC)=CC2=C1OCO2 FIPWRIJSWJWJAI-UHFFFAOYSA-N 0.000 description 4
125000003830 C1- C4 alkylcarbonylamino group Chemical group 0.000 description 4
XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical group [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 4
241000256248 Spodoptera Species 0.000 description 4
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 4
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125000004429 atom Chemical group 0.000 description 4
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 4
229910052794 bromium Inorganic materials 0.000 description 4
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238000001179 sorption measurement Methods 0.000 description 1
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238000001694 spray drying Methods 0.000 description 1
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HYVWIQDYBVKITD-UHFFFAOYSA-N tolylfluanid Chemical compound CN(C)S(=O)(=O)N(SC(F)(Cl)Cl)C1=CC=C(C)C=C1 HYVWIQDYBVKITD-UHFFFAOYSA-N 0.000 description 1
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125000004665 trialkylsilyl group Chemical group 0.000 description 1
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IQGKIPDJXCAMSM-UHFFFAOYSA-N triazoxide Chemical compound N=1C2=CC=C(Cl)C=C2[N+]([O-])=NC=1N1C=CN=C1 IQGKIPDJXCAMSM-UHFFFAOYSA-N 0.000 description 1
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DQJCHOQLCLEDLL-UHFFFAOYSA-N tricyclazole Chemical compound CC1=CC=CC2=C1N1C=NN=C1S2 DQJCHOQLCLEDLL-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
RROQIUMZODEXOR-UHFFFAOYSA-N triforine Chemical compound O=CNC(C(Cl)(Cl)Cl)N1CCN(C(NC=O)C(Cl)(Cl)Cl)CC1 RROQIUMZODEXOR-UHFFFAOYSA-N 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
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239000013598 vector Substances 0.000 description 1
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239000000080 wetting agent Substances 0.000 description 1
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