BE458857A - - Google Patents
Info
- Publication number
- BE458857A BE458857A BE458857DA BE458857A BE 458857 A BE458857 A BE 458857A BE 458857D A BE458857D A BE 458857DA BE 458857 A BE458857 A BE 458857A
- Authority
- BE
- Belgium
- Prior art keywords
- ether
- oxide
- parts
- phenyl
- chloro
- Prior art date
Links
- 125000005843 halogen group Chemical group 0.000 claims description 4
- 125000000217 alkyl group Chemical group 0.000 claims description 3
- 241000607479 Yersinia pestis Species 0.000 claims 1
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 6
- 241000238631 Hexapoda Species 0.000 description 5
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 5
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 4
- 125000003118 aryl group Chemical group 0.000 description 3
- 230000000749 insecticidal effect Effects 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- 125000000590 4-methylphenyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])([H])[H] 0.000 description 2
- 230000009471 action Effects 0.000 description 2
- 239000000853 adhesive Substances 0.000 description 2
- MHDVGSVTJDSBDK-UHFFFAOYSA-N dibenzyl ether Chemical class C=1C=CC=CC=1COCC1=CC=CC=C1 MHDVGSVTJDSBDK-UHFFFAOYSA-N 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- 229910052736 halogen Inorganic materials 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 description 2
- 244000045947 parasite Species 0.000 description 2
- -1 phenyl-butyl Chemical group 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 239000000454 talc Substances 0.000 description 2
- 229910052623 talc Inorganic materials 0.000 description 2
- QWUWMCYKGHVNAV-UHFFFAOYSA-N 1,2-dihydrostilbene Chemical group C=1C=CC=CC=1CCC1=CC=CC=C1 QWUWMCYKGHVNAV-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- OWYWGLHRNBIFJP-UHFFFAOYSA-N Ipazine Chemical compound CCN(CC)C1=NC(Cl)=NC(NC(C)C)=N1 OWYWGLHRNBIFJP-UHFFFAOYSA-N 0.000 description 1
- 230000002141 anti-parasite Effects 0.000 description 1
- 239000003096 antiparasitic agent Substances 0.000 description 1
- 125000003710 aryl alkyl group Chemical group 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
- 239000004359 castor oil Substances 0.000 description 1
- 235000019438 castor oil Nutrition 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 125000004188 dichlorophenyl group Chemical group 0.000 description 1
- 238000007865 diluting Methods 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 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 1
- 150000002367 halogens Chemical class 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 125000004430 oxygen atom Chemical group O* 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 125000004344 phenylpropyl group Chemical group 0.000 description 1
- 229940100486 rice starch Drugs 0.000 description 1
- 230000009476 short term action Effects 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
Landscapes
- Agricultural Chemicals And Associated Chemicals (AREA)
Publications (1)
| Publication Number | Publication Date |
|---|---|
| BE458857A true BE458857A (enExample) |
Family
ID=112064
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| BE458857D BE458857A (enExample) |
Country Status (1)
| Country | Link |
|---|---|
| BE (1) | BE458857A (enExample) |
-
0
- BE BE458857D patent/BE458857A/fr unknown
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| EP0070219B1 (fr) | Compositions herbicides à base de dérivés d'amino-4 chloro-6 alkylthio-5 pyrimidine et de dérivés de la dinitro-2,6 aniline et procédé de traitement des cultures à l'aide desdites compositions | |
| LU87728A1 (fr) | Compositions liquides concentrees a base de n-phosphonomethylglycine | |
| US4341548A (en) | N-(2-Cyclohexylphenyl)-N',N'-diethyl-ethylene diamine, algicidal compositions containing same, and method of use | |
| JPS6245860B2 (enExample) | ||
| CA1179802A (fr) | Composition biocide a base de sulfonium et de composes organiques de l'etain | |
| BE458857A (enExample) | ||
| FR2484199A1 (fr) | Composition mollusquicide a base de o-(benzothienyl-3 glyoxylonitriloximino) phosphate de o,o-dialkyle et procede de lutte contre les mollusques | |
| EP0569264B1 (fr) | Composition phytosanitaire hydrosoluble incorporant un dérivé de semisulfosuccinate | |
| BE458858A (enExample) | ||
| CA1201603A (fr) | Compositions herbicides a base de melanges contenant un derive d'acides phenoxybenzoiques | |
| FR2591593A1 (fr) | Composes heterocycliques oxygenes ou soufres de 5 a 7 chainons et substitues en position 2, compositions nematicides et insecticides les contenant et procede pour leur preparation | |
| WO1997004654A1 (fr) | Associations insecticides d'un oxime carbamate avec un insecticide a groupe pyrazole, pyrrole ou phenylimidazole | |
| LU85259A1 (fr) | Ester de l'hydroxyde de tricyclohexyletain acaricide | |
| FR2589327A1 (fr) | Melanges herbicides de derives d'acides pyridinoxyalcanoiques et de derives d'acides phenoxybenzoiques et leur utilisation pour le traitement des cultures | |
| BE538462A (enExample) | ||
| BE535600A (enExample) | ||
| CH319143A (fr) | Utilisation pour la lutte contre les acariens d'un sulfoxyde de phényle et de benzyle | |
| BE462879A (enExample) | ||
| BE460996A (enExample) | ||
| CH318716A (fr) | Utilisation pour la lutte contre les acariens d'un sulfure substitué de phényle et de benzyle | |
| BE432528A (enExample) | ||
| EP0080917B1 (fr) | Compositions herbicides à base de dérivés d'amino-4 chloro-6 alkylthio-5 pyrimidine et de pyridate, et procédé de traitement des cultures à l'aide desdites compositions | |
| EP0316245A1 (fr) | Dérivés nicotiniques fongicides | |
| LU81677A1 (fr) | Nouveaux derives de l'oxadiazoline-1,3,4 one-5,leur preparation et les compositions insecticides les contenant | |
| FR2648317A1 (fr) | Compositions liquides concentrees a base de n-phosphonomethylglycine |