JPS61233604A

JPS61233604A - 除草剤組成物

除草剤組成物

Info

Publication number: JPS61233604A
Authority: JP; Japan
Prior art keywords: parts; compound; benzyl; alkyl; lower alkyl
Prior art date: 1985-04-09
Legal status : Granted

Application number

JP60074961A

Other languages

English (en)

Japanese (ja)

Other versions

JPH0477721B2 (enrdf_load_html_response

Inventor

Takashi Igai

猪飼　隆

Current Assignee

Nissan Chemical Corp

Original Assignee

Nissan Chemical Corp

Priority date

1985-04-09

Filing date

1985-04-09

Publication date

1986-10-17

1985-04-09 Application filed by Nissan Chemical Corp filed Critical Nissan Chemical Corp

1985-04-09 Priority to JP60074961A priority Critical patent/JPS61233604A/ja

1986-02-18 Priority to KR1019860001105A priority patent/KR930002954B1/ko

1986-10-17 Publication of JPS61233604A publication Critical patent/JPS61233604A/ja

1992-12-09 Publication of JPH0477721B2 publication Critical patent/JPH0477721B2/ja

Status Granted legal-status Critical Current

Links

239000000203 mixture Substances 0.000 title claims abstract description 20
230000002363 herbicidal effect Effects 0.000 title claims abstract description 17
239000004009 herbicide Substances 0.000 title claims abstract description 14
125000000217 alkyl group Chemical group 0.000 claims abstract description 12
125000003545 alkoxy group Chemical group 0.000 claims abstract description 6
VMFDZAIIYSKZDE-UHFFFAOYSA-N 1h-pyrazol-5-ylsulfonylurea Chemical compound NC(=O)NS(=O)(=O)C=1C=CNN=1 VMFDZAIIYSKZDE-UHFFFAOYSA-N 0.000 claims abstract description 4
239000004480 active ingredient Substances 0.000 claims description 4
239000000126 substance Substances 0.000 claims description 3
KXDHJXZQYSOELW-UHFFFAOYSA-M Carbamate Chemical compound NC([O-])=O KXDHJXZQYSOELW-UHFFFAOYSA-M 0.000 claims description 2
125000005843 halogen group Chemical group 0.000 claims description 2
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 2
229910052757 nitrogen Inorganic materials 0.000 claims description 2
125000004433 nitrogen atom Chemical group N* 0.000 claims description 2
150000001875 compounds Chemical class 0.000 abstract description 40
241000196324 Embryophyta Species 0.000 abstract description 23
230000002195 synergetic effect Effects 0.000 abstract description 8
229910052736 halogen Inorganic materials 0.000 abstract 1
150000002367 halogens Chemical class 0.000 abstract 1
239000008187 granular material Substances 0.000 description 21
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 15
230000000694 effects Effects 0.000 description 12
239000000454 talc Substances 0.000 description 12
229910052623 talc Inorganic materials 0.000 description 12
238000001125 extrusion Methods 0.000 description 10
229940126062 Compound A Drugs 0.000 description 7
NLDMNSXOCDLTTB-UHFFFAOYSA-N Heterophylliin A Natural products O1C2COC(=O)C3=CC(O)=C(O)C(O)=C3C3=C(O)C(O)=C(O)C=C3C(=O)OC2C(OC(=O)C=2C=C(O)C(O)=C(O)C=2)C(O)C1OC(=O)C1=CC(O)=C(O)C(O)=C1 NLDMNSXOCDLTTB-UHFFFAOYSA-N 0.000 description 7
244000025254 Cannabis sativa Species 0.000 description 6
241000209094 Oryza Species 0.000 description 5
238000003756 stirring Methods 0.000 description 5
244000058871 Echinochloa crus-galli Species 0.000 description 4
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239000003795 chemical substances by application Substances 0.000 description 2
238000009472 formulation Methods 0.000 description 2
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238000004898 kneading Methods 0.000 description 2
238000002156 mixing Methods 0.000 description 2
238000010298 pulverizing process Methods 0.000 description 2
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QIVUCLWGARAQIO-OLIXTKCUSA-N (3s)-n-[(3s,5s,6r)-6-methyl-2-oxo-1-(2,2,2-trifluoroethyl)-5-(2,3,6-trifluorophenyl)piperidin-3-yl]-2-oxospiro[1h-pyrrolo[2,3-b]pyridine-3,6'-5,7-dihydrocyclopenta[b]pyridine]-3'-carboxamide Chemical compound C1([C@H]2[C@H](N(C(=O)[C@@H](NC(=O)C=3C=C4C[C@]5(CC4=NC=3)C3=CC=CN=C3NC5=O)C2)CC(F)(F)F)C)=C(F)C=CC(F)=C1F QIVUCLWGARAQIO-OLIXTKCUSA-N 0.000 description 1
241001638133 Bidyanus welchi Species 0.000 description 1
201000004569 Blindness Diseases 0.000 description 1
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244000239348 Echinochloa crus galli var. praticola Species 0.000 description 1
241000254158 Lampyridae Species 0.000 description 1
240000008114 Panicum miliaceum Species 0.000 description 1
235000007199 Panicum miliaceum Nutrition 0.000 description 1
239000004698 Polyethylene Substances 0.000 description 1
241000208422 Rhododendron Species 0.000 description 1
241000681978 Rhododendron japonicum Species 0.000 description 1
244000062793 Sorghum vulgare Species 0.000 description 1
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238000006243 chemical reaction Methods 0.000 description 1
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239000003085 diluting agent Substances 0.000 description 1
239000002552 dosage form Substances 0.000 description 1
230000008030 elimination Effects 0.000 description 1
238000003379 elimination reaction Methods 0.000 description 1
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
238000002474 experimental method Methods 0.000 description 1
239000013505 freshwater Substances 0.000 description 1
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