NO741906L - - Google Patents
Info
- Publication number
- NO741906L NO741906L NO741906A NO741906A NO741906L NO 741906 L NO741906 L NO 741906L NO 741906 A NO741906 A NO 741906A NO 741906 A NO741906 A NO 741906A NO 741906 L NO741906 L NO 741906L
- Authority
- NO
- Norway
- Prior art keywords
- substituted
- salt
- benzothiadiazinone
- dioxide
- methyl
- Prior art date
Links
- 150000003839 salts Chemical class 0.000 claims description 24
- 239000000203 mixture Substances 0.000 claims description 21
- 150000001875 compounds Chemical class 0.000 claims description 19
- 230000002363 herbicidal effect Effects 0.000 claims description 10
- 229910052739 hydrogen Inorganic materials 0.000 claims description 10
- 239000001257 hydrogen Substances 0.000 claims description 10
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 9
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 8
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 8
- 125000000217 alkyl group Chemical group 0.000 claims description 6
- 229910052736 halogen Inorganic materials 0.000 claims description 6
- 150000002367 halogens Chemical class 0.000 claims description 6
- 239000004009 herbicide Substances 0.000 claims description 5
- 125000003545 alkoxy group Chemical group 0.000 claims description 2
- 150000002431 hydrogen Chemical class 0.000 claims description 2
- CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical compound [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 claims 1
- -1 cycloalkyl radical Chemical class 0.000 description 30
- 239000013543 active substance Substances 0.000 description 21
- 150000002148 esters Chemical class 0.000 description 19
- 241000196324 Embryophyta Species 0.000 description 16
- 150000001408 amides Chemical class 0.000 description 15
- 239000003795 chemical substances by application Substances 0.000 description 11
- 239000003921 oil Substances 0.000 description 10
- 159000000000 sodium salts Chemical class 0.000 description 8
- XBDQKXXYIPTUBI-UHFFFAOYSA-N Propionic acid Substances CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 7
- 239000002253 acid Substances 0.000 description 7
- 150000007513 acids Chemical class 0.000 description 7
- 239000006185 dispersion Substances 0.000 description 7
- 239000000126 substance Substances 0.000 description 7
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 5
- WBCZYGZZXCPBAO-UHFFFAOYSA-M 1,2-dimethyl-3,4-diphenylpyrazol-1-ium methyl sulfate Chemical compound S(=O)(=O)(OC)[O-].C[N+]=1N(C(=C(C1)C1=CC=CC=C1)C1=CC=CC=C1)C WBCZYGZZXCPBAO-UHFFFAOYSA-M 0.000 description 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
- 239000012876 carrier material Substances 0.000 description 4
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 4
- 239000000839 emulsion Substances 0.000 description 4
- 230000012010 growth Effects 0.000 description 4
- 239000000843 powder Substances 0.000 description 4
- 239000007787 solid Substances 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- SLCGUGMPSUYJAY-UHFFFAOYSA-N Benzoylprop-ethyl Chemical compound C=1C=C(Cl)C(Cl)=CC=1N(C(C)C(=O)OCC)C(=O)C1=CC=CC=C1 SLCGUGMPSUYJAY-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 239000003513 alkali Substances 0.000 description 3
- 235000013877 carbamide Nutrition 0.000 description 3
- 239000008187 granular material Substances 0.000 description 3
- 229920000151 polyglycol Polymers 0.000 description 3
- 239000010695 polyglycol Substances 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 2
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 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
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- 239000000853 adhesive Substances 0.000 description 2
- 230000001070 adhesive effect Effects 0.000 description 2
- 150000003863 ammonium salts Chemical class 0.000 description 2
- 230000000844 anti-bacterial effect Effects 0.000 description 2
- 239000000729 antidote Substances 0.000 description 2
- 229940075522 antidotes Drugs 0.000 description 2
- 239000003899 bactericide agent Substances 0.000 description 2
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 2
- 239000004927 clay Substances 0.000 description 2
- 239000012141 concentrate Substances 0.000 description 2
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
- PAFZNILMFXTMIY-UHFFFAOYSA-N cyclohexylamine Chemical compound NC1CCCCC1 PAFZNILMFXTMIY-UHFFFAOYSA-N 0.000 description 2
- 239000002270 dispersing agent Substances 0.000 description 2
- 239000003995 emulsifying agent Substances 0.000 description 2
- 239000000417 fungicide Substances 0.000 description 2
- 239000003630 growth substance Substances 0.000 description 2
- 239000002917 insecticide Substances 0.000 description 2
- HJOVHMDZYOCNQW-UHFFFAOYSA-N isophorone Chemical compound CC1=CC(=O)CC(C)(C)C1 HJOVHMDZYOCNQW-UHFFFAOYSA-N 0.000 description 2
- 229920005610 lignin Polymers 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 230000001069 nematicidal effect Effects 0.000 description 2
- 239000005645 nematicide Substances 0.000 description 2
- YDCVQGAUCOROHB-UHFFFAOYSA-N oxadiazolidine-4,5-dione Chemical class O=C1NNOC1=O YDCVQGAUCOROHB-UHFFFAOYSA-N 0.000 description 2
- 239000006072 paste Substances 0.000 description 2
- SIOXPEMLGUPBBT-UHFFFAOYSA-N picolinic acid Chemical class OC(=O)C1=CC=CC=N1 SIOXPEMLGUPBBT-UHFFFAOYSA-N 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- 239000002689 soil Substances 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 2
- 150000003672 ureas Chemical class 0.000 description 2
- 235000013311 vegetables Nutrition 0.000 description 2
- FNQJDLTXOVEEFB-UHFFFAOYSA-N 1,2,3-benzothiadiazole Chemical class C1=CC=C2SN=NC2=C1 FNQJDLTXOVEEFB-UHFFFAOYSA-N 0.000 description 1
- CSNIZNHTOVFARY-UHFFFAOYSA-N 1,2-benzothiazole Chemical class C1=CC=C2C=NSC2=C1 CSNIZNHTOVFARY-UHFFFAOYSA-N 0.000 description 1
- XQEMNBNCQVQXMO-UHFFFAOYSA-M 1,2-dimethyl-3,5-diphenylpyrazol-1-ium;methyl sulfate Chemical compound COS([O-])(=O)=O.C[N+]=1N(C)C(C=2C=CC=CC=2)=CC=1C1=CC=CC=C1 XQEMNBNCQVQXMO-UHFFFAOYSA-M 0.000 description 1
- GEYOCULIXLDCMW-UHFFFAOYSA-N 1,2-phenylenediamine Chemical compound NC1=CC=CC=C1N GEYOCULIXLDCMW-UHFFFAOYSA-N 0.000 description 1
- MFVFDTCSVFBOTL-UHFFFAOYSA-N 1,3-diazetidine Chemical class C1NCN1 MFVFDTCSVFBOTL-UHFFFAOYSA-N 0.000 description 1
- GUSTUIJJPMXTTI-UHFFFAOYSA-N 1-dodecylazepane Chemical class CCCCCCCCCCCCN1CCCCCC1 GUSTUIJJPMXTTI-UHFFFAOYSA-N 0.000 description 1
- XUJLWPFSUCHPQL-UHFFFAOYSA-N 11-methyldodecan-1-ol Chemical compound CC(C)CCCCCCCCCCO XUJLWPFSUCHPQL-UHFFFAOYSA-N 0.000 description 1
- QTBPKHDDRYSMMU-UHFFFAOYSA-N 1H-pyrazol-1-ium sulfate Chemical class S(=O)(=O)([O-])[O-].[NH2+]1N=CC=C1.[NH2+]1N=CC=C1 QTBPKHDDRYSMMU-UHFFFAOYSA-N 0.000 description 1
- JCRNSBKSAQHNIN-UHFFFAOYSA-N 2,4-dibutylnaphthalene-1-sulfonic acid Chemical class C1=CC=CC2=C(S(O)(=O)=O)C(CCCC)=CC(CCCC)=C21 JCRNSBKSAQHNIN-UHFFFAOYSA-N 0.000 description 1
- FDMDZIBZKGXZPT-UHFFFAOYSA-N 2-(2,4-dichlorophenoxy)acetic acid;2-(2-hydroxyethylamino)ethanol Chemical compound OCCNCCO.OC(=O)COC1=CC=C(Cl)C=C1Cl FDMDZIBZKGXZPT-UHFFFAOYSA-N 0.000 description 1
- WRXSEWUFHVTFEX-UHFFFAOYSA-N 2-(2,4-dichlorophenoxy)propanoate;dimethylazanium Chemical compound CNC.OC(=O)C(C)OC1=CC=C(Cl)C=C1Cl WRXSEWUFHVTFEX-UHFFFAOYSA-N 0.000 description 1
- ZGWNXHRVUJVMCP-UHFFFAOYSA-N 2-(2-chlorophenoxy)propanoic acid Chemical compound OC(=O)C(C)OC1=CC=CC=C1Cl ZGWNXHRVUJVMCP-UHFFFAOYSA-N 0.000 description 1
- PAWQVTBBRAZDMG-UHFFFAOYSA-N 2-(3-bromo-2-fluorophenyl)acetic acid Chemical compound OC(=O)CC1=CC=CC(Br)=C1F PAWQVTBBRAZDMG-UHFFFAOYSA-N 0.000 description 1
- QTDIEDOANJISNP-UHFFFAOYSA-N 2-dodecoxyethyl hydrogen sulfate Chemical class CCCCCCCCCCCCOCCOS(O)(=O)=O QTDIEDOANJISNP-UHFFFAOYSA-N 0.000 description 1
- REEXLQXWNOSJKO-UHFFFAOYSA-N 2h-1$l^{4},2,3-benzothiadiazine 1-oxide Chemical compound C1=CC=C2S(=O)NN=CC2=C1 REEXLQXWNOSJKO-UHFFFAOYSA-N 0.000 description 1
- UOCUSOBVEHOMMB-UHFFFAOYSA-N 2h-1$l^{6},2,3-benzothiadiazine 1,1-dioxide Chemical class C1=CC=C2S(=O)(=O)NN=CC2=C1 UOCUSOBVEHOMMB-UHFFFAOYSA-N 0.000 description 1
- HQQTZCPKNZVLFF-UHFFFAOYSA-N 4h-1,2-benzoxazin-3-one Chemical class C1=CC=C2ONC(=O)CC2=C1 HQQTZCPKNZVLFF-UHFFFAOYSA-N 0.000 description 1
- 241000219496 Alnus Species 0.000 description 1
- 239000005995 Aluminium silicate Substances 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- 239000004254 Ammonium phosphate Substances 0.000 description 1
- 240000002791 Brassica napus Species 0.000 description 1
- 235000011293 Brassica napus Nutrition 0.000 description 1
- WUFYJSIFTHYAGJ-UHFFFAOYSA-N C=1C=NSC=1.O=C1N=CC=CN1 Chemical class C=1C=NSC=1.O=C1N=CC=CN1 WUFYJSIFTHYAGJ-UHFFFAOYSA-N 0.000 description 1
- 241000207199 Citrus Species 0.000 description 1
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 1
- 235000014493 Crataegus Nutrition 0.000 description 1
- 241001092040 Crataegus Species 0.000 description 1
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 1
- ROSDSFDQCJNGOL-UHFFFAOYSA-N Dimethylamine Chemical compound CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 description 1
- 241000551547 Dione <red algae> Species 0.000 description 1
- QUSNBJAOOMFDIB-UHFFFAOYSA-N Ethylamine Chemical compound CCN QUSNBJAOOMFDIB-UHFFFAOYSA-N 0.000 description 1
- ZLSWBLPERHFHIS-UHFFFAOYSA-N Fenoprop Chemical compound OC(=O)C(C)OC1=CC(Cl)=C(Cl)C=C1Cl ZLSWBLPERHFHIS-UHFFFAOYSA-N 0.000 description 1
- 241000246169 Genista Species 0.000 description 1
- 241000209219 Hordeum Species 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 239000005909 Kieselgur Substances 0.000 description 1
- 241000735235 Ligustrum vulgare Species 0.000 description 1
- 241000209510 Liliopsida Species 0.000 description 1
- 235000019738 Limestone Nutrition 0.000 description 1
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- BAVYZALUXZFZLV-UHFFFAOYSA-N Methylamine Chemical compound NC BAVYZALUXZFZLV-UHFFFAOYSA-N 0.000 description 1
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 1
- 229930192627 Naphthoquinone Natural products 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 240000007594 Oryza sativa Species 0.000 description 1
- 235000007164 Oryza sativa Nutrition 0.000 description 1
- 241000219833 Phaseolus Species 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 241000209504 Poaceae Species 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
- 239000004721 Polyphenylene oxide Substances 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- WTKZEGDFNFYCGP-UHFFFAOYSA-N Pyrazole Chemical class C=1C=NNC=1 WTKZEGDFNFYCGP-UHFFFAOYSA-N 0.000 description 1
- 241000220324 Pyrus Species 0.000 description 1
- 235000011483 Ribes Nutrition 0.000 description 1
- 241000220483 Ribes Species 0.000 description 1
- 244000082988 Secale cereale Species 0.000 description 1
- 235000007238 Secale cereale Nutrition 0.000 description 1
- 244000061456 Solanum tuberosum Species 0.000 description 1
- 235000002595 Solanum tuberosum Nutrition 0.000 description 1
- 241000907897 Tilia Species 0.000 description 1
- 235000011941 Tilia x europaea Nutrition 0.000 description 1
- 235000021307 Triticum Nutrition 0.000 description 1
- 241000209140 Triticum Species 0.000 description 1
- 241001106462 Ulmus Species 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
- 235000009392 Vitis Nutrition 0.000 description 1
- 241000219095 Vitis Species 0.000 description 1
- 240000008042 Zea mays Species 0.000 description 1
- 235000007244 Zea mays Nutrition 0.000 description 1
- DHKHKXVYLBGOIT-UHFFFAOYSA-N acetaldehyde Diethyl Acetal Natural products CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000007933 aliphatic carboxylic acids Chemical class 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 125000002877 alkyl aryl group Chemical group 0.000 description 1
- 150000005215 alkyl ethers Chemical class 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 229910000148 ammonium phosphate Inorganic materials 0.000 description 1
- 235000019289 ammonium phosphates Nutrition 0.000 description 1
- BFNBIHQBYMNNAN-UHFFFAOYSA-N ammonium sulfate Chemical compound N.N.OS(O)(=O)=O BFNBIHQBYMNNAN-UHFFFAOYSA-N 0.000 description 1
- 229910052921 ammonium sulfate Inorganic materials 0.000 description 1
- 239000001166 ammonium sulphate Substances 0.000 description 1
- 235000011130 ammonium sulphate Nutrition 0.000 description 1
- 150000001448 anilines Chemical class 0.000 description 1
- 239000002518 antifoaming agent Substances 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- BUSBFZWLPXDYIC-UHFFFAOYSA-N arsonic acid Chemical class O[AsH](O)=O BUSBFZWLPXDYIC-UHFFFAOYSA-N 0.000 description 1
- 125000003785 benzimidazolyl group Chemical class N1=C(NC2=C1C=CC=C2)* 0.000 description 1
- 150000005130 benzoxazines Chemical class 0.000 description 1
- 230000004071 biological effect Effects 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 159000000007 calcium salts Chemical class 0.000 description 1
- OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Inorganic materials [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 description 1
- 239000001175 calcium sulphate Substances 0.000 description 1
- 235000011132 calcium sulphate Nutrition 0.000 description 1
- 150000004657 carbamic acid derivatives Chemical class 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 239000004359 castor oil Substances 0.000 description 1
- 235000019438 castor oil Nutrition 0.000 description 1
- 235000013339 cereals Nutrition 0.000 description 1
- 235000019987 cider Nutrition 0.000 description 1
- 235000020971 citrus fruits Nutrition 0.000 description 1
- 239000011280 coal tar Substances 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- HPXRVTGHNJAIIH-UHFFFAOYSA-N cyclohexanol Chemical compound OC1CCCCC1 HPXRVTGHNJAIIH-UHFFFAOYSA-N 0.000 description 1
- 150000003946 cyclohexylamines Chemical class 0.000 description 1
- MNNHAPBLZZVQHP-UHFFFAOYSA-N diammonium hydrogen phosphate Chemical compound [NH4+].[NH4+].OP([O-])([O-])=O MNNHAPBLZZVQHP-UHFFFAOYSA-N 0.000 description 1
- 150000001991 dicarboxylic acids Chemical class 0.000 description 1
- 239000002283 diesel fuel Substances 0.000 description 1
- HPNMFZURTQLUMO-UHFFFAOYSA-N diethylamine Chemical compound CCNCC HPNMFZURTQLUMO-UHFFFAOYSA-N 0.000 description 1
- 238000007865 diluting Methods 0.000 description 1
- 150000004656 dimethylamines Chemical class 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 150000002019 disulfides Chemical class 0.000 description 1
- LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 description 1
- 239000010459 dolomite Substances 0.000 description 1
- 229910000514 dolomite Inorganic materials 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 150000002169 ethanolamines Chemical class 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- QQSGDKKFXBGYON-UHFFFAOYSA-N ethoxy-methylperoxy-(6-methyl-2-propan-2-ylpyrimidin-4-yl)oxy-sulfanylidene-$l^{5}-phosphane Chemical class CCOP(=S)(OOC)OC1=CC(C)=NC(C(C)C)=N1 QQSGDKKFXBGYON-UHFFFAOYSA-N 0.000 description 1
- 241001233957 eudicotyledons Species 0.000 description 1
- 239000003337 fertilizer Substances 0.000 description 1
- 235000013312 flour Nutrition 0.000 description 1
- 235000011389 fruit/vegetable juice Nutrition 0.000 description 1
- 239000000499 gel Substances 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
- 238000000227 grinding Methods 0.000 description 1
- 150000001469 hydantoins Chemical class 0.000 description 1
- 229940042795 hydrazides for tuberculosis treatment Drugs 0.000 description 1
- 150000002429 hydrazines Chemical class 0.000 description 1
- 150000002460 imidazoles Chemical class 0.000 description 1
- 238000005470 impregnation Methods 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- 239000003350 kerosene Substances 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 239000004571 lime Substances 0.000 description 1
- 239000006028 limestone Substances 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- 229910003002 lithium salt Inorganic materials 0.000 description 1
- 159000000002 lithium salts Chemical class 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000000395 magnesium oxide Substances 0.000 description 1
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 1
- 235000012245 magnesium oxide Nutrition 0.000 description 1
- 159000000003 magnesium salts Chemical class 0.000 description 1
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 1
- 235000019341 magnesium sulphate Nutrition 0.000 description 1
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 150000003956 methylamines Chemical class 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 235000010981 methylcellulose Nutrition 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 235000010755 mineral Nutrition 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- PSZYNBSKGUBXEH-UHFFFAOYSA-N naphthalene-1-sulfonic acid Chemical class C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-N 0.000 description 1
- 150000002790 naphthalenes Chemical class 0.000 description 1
- 150000002791 naphthoquinones Chemical class 0.000 description 1
- QNMLMAVEXUCXRG-UHFFFAOYSA-N oxadiazinane-4,5-dione Chemical class O=C1CONNC1=O QNMLMAVEXUCXRG-UHFFFAOYSA-N 0.000 description 1
- SDRLFDJOSQLRPB-UHFFFAOYSA-N oxadiazine-4,5-dione Chemical class O=C1CON=NC1=O SDRLFDJOSQLRPB-UHFFFAOYSA-N 0.000 description 1
- 150000004866 oxadiazoles Chemical class 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- REJGOFYVRVIODZ-UHFFFAOYSA-N phosphanium;chloride Chemical class P.Cl REJGOFYVRVIODZ-UHFFFAOYSA-N 0.000 description 1
- AQSJGOWTSHOLKH-UHFFFAOYSA-N phosphite(3-) Chemical class [O-]P([O-])[O-] AQSJGOWTSHOLKH-UHFFFAOYSA-N 0.000 description 1
- 150000003009 phosphonic acids Chemical class 0.000 description 1
- 235000011007 phosphoric acid Nutrition 0.000 description 1
- 150000003016 phosphoric acids Chemical class 0.000 description 1
- 150000003053 piperidines Chemical class 0.000 description 1
- 230000008635 plant growth Effects 0.000 description 1
- 239000002798 polar solvent Substances 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- 150000003217 pyrazoles Chemical class 0.000 description 1
- 150000004892 pyridazines Chemical class 0.000 description 1
- 150000003222 pyridines Chemical class 0.000 description 1
- 150000005299 pyridinones Chemical class 0.000 description 1
- 150000003230 pyrimidines Chemical class 0.000 description 1
- 150000008318 pyrimidones Chemical class 0.000 description 1
- NYCVCXMSZNOGDH-UHFFFAOYSA-N pyrrolidine-1-carboxylic acid Chemical class OC(=O)N1CCCC1 NYCVCXMSZNOGDH-UHFFFAOYSA-N 0.000 description 1
- 150000003235 pyrrolidines Chemical class 0.000 description 1
- 150000004040 pyrrolidinones Chemical class 0.000 description 1
- 125000002294 quinazolinyl group Chemical class N1=C(N=CC2=CC=CC=C12)* 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 210000000614 rib Anatomy 0.000 description 1
- 239000000741 silica gel Substances 0.000 description 1
- 229910002027 silica gel Inorganic materials 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- 125000005624 silicic acid group Chemical class 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- MMKVIBJBAFUGNG-UHFFFAOYSA-M sodium;2-(4-chloro-2-methylphenoxy)butanoate Chemical compound [Na+].CCC(C([O-])=O)OC1=CC=C(Cl)C=C1C MMKVIBJBAFUGNG-UHFFFAOYSA-M 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- 238000009331 sowing Methods 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 238000003892 spreading Methods 0.000 description 1
- 125000003011 styrenyl group Chemical class [H]\C(*)=C(/[H])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-L sulfite Chemical compound [O-]S([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-L 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-N sulfonic acid Chemical compound OS(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-N 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- CXWXQJXEFPUFDZ-UHFFFAOYSA-N tetralin Chemical compound C1=CC=C2CCCCC2=C1 CXWXQJXEFPUFDZ-UHFFFAOYSA-N 0.000 description 1
- OLPRIZQBWZMBAS-UHFFFAOYSA-N thiadiazolidine 1,1-dioxide Chemical class O=S1(=O)CCNN1 OLPRIZQBWZMBAS-UHFFFAOYSA-N 0.000 description 1
- 150000003566 thiocarboxylic acids Chemical class 0.000 description 1
- 150000003582 thiophosphoric acids Chemical class 0.000 description 1
- 150000003585 thioureas Chemical class 0.000 description 1
- 239000011573 trace mineral Substances 0.000 description 1
- 235000013619 trace mineral Nutrition 0.000 description 1
- 150000003918 triazines Chemical class 0.000 description 1
- 150000003852 triazoles Chemical class 0.000 description 1
- GETQZCLCWQTVFV-UHFFFAOYSA-N trimethylamine Chemical compound CN(C)C GETQZCLCWQTVFV-UHFFFAOYSA-N 0.000 description 1
- 244000045561 useful plants Species 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 239000008096 xylene 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
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
- A01N43/56—1,2-Diazoles; Hydrogenated 1,2-diazoles
-
- 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
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
- A01N47/28—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N<
- A01N47/30—Derivatives containing the group >N—CO—N aryl or >N—CS—N—aryl
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Description
"Herbicide midler"
Den foreliggende oppfinnelse angår verdifulle nye herbi-
cider som inneholder en blanding av forskjéllige virksomme stoffer.
Det er kjent at urinstoffer, pyrazoliumsulfater, etyl-N-benzbyl-N- (3',-4-diklorfenyl) -2-aminopropionat, m-klorfényl-karba-minsyre-4-klor-butin-2-yl-l-ester, a-klor-B-(4-klorfenyl)-propionsyremetylester, benzotiadiazinon-dioksyder og fenoksykarboksyl^
syrer har en herbicid virkning. Deres herbicide virkning er imid-
lertid ikke alltid tilstrekkelig.
Det ble funnet at en blanding av
a) en forbindelse med formelen
hvor X be£yr metoksy når betyr metoksy og R betyr hydrogen, og hvor X betyr metyl, metoksy eller halogen, når R betyr en
cykloalkylrest og R^ betyr metyl, hydrogen eller metoksy, \ F~\ og/eller
b) en forbindelse med formelen
hvor R betyr alkyloksy eller en eventuelt med halogen eller
metyl substituert fenylrest, og/eller
c) forbindelsen
og/eller
d) forbindelsen
og/eller
e) forbindelsen
og/eller
f) en forbindelse med formelen
hvor R betyr lavere alkyl, R^ betyr hydrogen eller saltene, for eksempel natrium-, litium-, kalium-, ammonium-, kalsium-, magnesium-, metylamin-, dimetylamin-, trimetylamin-, etyl-amin-, dietylamin-, etSnolamin-, dietanolamin-, anilin-, ^pyridin-, hydrazin-, fenylendiamin-, cykloheksylamin-, dode-cylheksametylenimin-saltet, og/eller
g) en forbindelse med formelen
hvor X betyr halogen eller metyl, R betyr hydrogen eller
alkyl, n har verdier fra 0 til 3, m har verdier fra 0 til 2,
R^ betyr alkyl, hydrogen eller saltene,
har en bedre herbicid virkning enn de virksomme enkeltstoffer!.
Blandingene kan inneholde en eller flere forbindelser med formelen a og forbindelser med formelen b, c, d, e, fogg.
Blandingsforholdet er 0,1-10 deler a til 1 del av de andre virksomme stoffer (vektdeler).
Den mengde som anvendes av midlene ifølge oppfinnelsen, kan variere. Den mengde som anvendes avhenger hovedsakelig av arten av den ønskede virkning. Mengden ligger vanligvis mellom 0,1 og 30 eller mer, fortrinnsvis 0,2-6 kg virksomt stoff pr. hektar. Midlene ifølge oppfinnelsen kan blant annet anvendes ved metoder hvor de påføres før plantingen, etter plantingen, før såingen, før eller etter at kulturplantene eller de uønskede planter er kommet opp av jorden, eller mens de er i ferd med å komme opp av jorden, og midlene kan anvendes en eller flere ganger.
Blandingene er egnet til bekjempelse av uønskede planter i kulturer av nytteplanter, som for eksempel Triticum spp., Hordeum spp., Secale cereale, Zea mays, Beta spp., Oryza sativa, Solanum tuberosum, pisunDsativum, Phaseolus spp., Brassica napus,[Glyine max., Genista spp., crataegus-spp., Alnusspp., Tilia spp., Citrus spp., Ligustrum vulgare, Pyrus spp., Ribes spp., Ulmus spp., Vitis viriifera,
Dessuten kan blandingen anvendes som totalmiddel ved graver, langs elver og bekker, langs jernbaneskinner, på øde flater etc.
Blandingene a+b+c, a+b+d, a+b+e, a+b+g, a+b + f, a + c + d, a + c + e, a + c + f, a + c + g, a + d.+ e,
a + d + f, a + d + g, a + e + f, a+e+g, b+c+d, b+c+e,
b + c + f, b + c + g, b + d + e, b + d + g, c + d + e, c + d + f,
c + d + gy c + f + g, d + e + f, d + e + g, d + f + g, e + f + g,
a + b, a + c, a + d, a + e, \b\+ c, b + d, b + e, b + g, c + d,
c + e, c + g,- d + e, d + f, e + f, e + g foretrekkes.
Midlene anvendes eksempelvis i form av direkte sprøytbare løsninger, pulvere, suspensjoner eller dispersjoner, emulsjoner,
oljedispersjoner, pastaer, støvformige midler, strømidler eller granulater, ved utsprøyting, forstøvning, utstrøing eller uthelling.
Bruksformene retter .seg helt etter anvendelsesformålet % |marT\tar imidlertid alltid sikte på en mest mulig fin fordeling av de virksomme stoffer ifølge oppfinnelsen.
For fremstilling av direkte sprøytbare løsninger, emulsjoner, pastaer og oljedispersjoner kan man bruke mineraloljefraksjoner med midlere til høyt kokepunkt, så som kerosin eller dieselolje, enn-videre kulltjæreoljer etc, samt oljer av vegetabilsk eller animalsk opprinnelse, alifatiske, cykliske og aromatiske hydrokarboner, for eksempel benzen, toluen, xylen, paraffin, tetrahydronaftalin, alky-lerte naftaliner eller derivater derav, for eksempel metanol, etanol,
propanol, butanol, kloroform, karbontetraklorid, cykloheksanol, cykloheksanon, klorbenzen, isoforon etc, sterkt polare løsningsmidler som for eksempel dimetylformamid, dimetylsulfoksyd, N-metylpyrrolidon, vann etc.
Vandige bruksformer kan fremstilles av emulsjonskonsentrater, pastaer eller fuktbare pulvere (sprøytepulvere) eller oljedispersjoner ved tilsetning av vann. Ved fremstilling av emulsjoner, pastaer eller oljedispersjoner kan stoffene som sådanne eller oppløst i olje eller løsningsmiddel (homogeniseres i vann ved hjelp av fukte-, klebe-, dispergerings- eller emulgeringsmidler. Det kan imidlertid også fremstilles konsentrater bestående av vi^rlcsomt stoff, fukte-, klebe-, dispergerings- eller emulgeringsmiddel og eventuelt løsnings-middel eller olje, hvilke konsentrater er egnet til å fortynnes med vann.
Blant overflateaktive stoffer kan nevnes: alkali-, jordal-kali- og ammoniumsalter av ligninsulfonsyre, naftalinsulfonsyrer, fenolsulfonsyrer,.alkylarylsulfonater, alkylsulfater, alkylsulfona-ter, alkali- og jordalkalisalter av dibutylnaftalinsulfonsyre, lau-ryletersulfat, fettalkoholsulfater, fettsufe alkali- og jordalkali-\salter,. salter av sulfaterte heksadekanoler, heptadekanoler, okta-dekanoler, salter av sulfatert fettalkoholglykoleter, kondensasjons- produkter av sulfonert naftalin og naftalinderivater med formaldehyd, kondensasjonspsrodukter av naftalin eller naftalinsulfonsyrer med fenol og formaldehyd, polyoksy^tylen-oktylfenoleter/ etoksylert isooktylfenol, -oktylfenol, -nonylfenofT^alkylfenolpolyglykoleter, tributylfenylpolyglykoleter, alkylarylpolyeteralkoholer, isotri-decylalkohol, fettalkoholetylenoksyd-kondensater, etoksylert rici-nusolje, polyoksyetylenalkyleter, etoksylert polyoksypropylen, laurylalkoliolpolyglykoleteracetal, sorbitolester, lignin, sulfitt-avluter og metylcellulose.
Pulver, strø- og støvformige midler kan fremstilles ved blanding eller sammaling av de Virksomme stoffer med et fast bære-materiale. Granulater, for eksempel omhyllings-, impregnerings-og homogengranulater, kan fremstilles ved binding av de virksomme stoffer på faste bærematerialer, faste bærematerialer er for eksempel mineralmaterialer så som silicagel, kiselsyrer, kiselgeler, silikater, talkum, kaolin, attaclay, kalkstein, kalk, kritt, bolus, løss, leire, dolomitt, diatoméjord, kalsium- og magnesiumsulfat, magnesiumoksyd, malte harpikser, gjødningsstoffer som for eksempel ammoniumsulfat, ammoniumfosfat, ammoniumnitrat, urinstoffer og vegetabilske produkter så som mel av korn, bark, tre og nøtteskall, cellulosepulver og andre faste bærematerialer.
iPrbparatene inneholder.mellom 0,1 og 95 vekt% virksomt stoff,
fortrinnsvis mellom 0,5 og 90 vekt%.
Til blandingene eller de enkelte virksomme stoffer kan man, eventuelt først umiddelbart før anvendelsen (tankblanding), tilsette oljer av forskjellige typer, herbicider, fungicider, nematocider, insekticider, baktericider, sporelementer, gjødningsstoffer, skum-hindrende midler (for eksempel silikoner), vekstregulatorer, motgiftmidler eller andre herbicid virksomme forbindelser, som fo[rVe,k-sempel
substituerte aniliner
substituerte aryloksykarboksylsyrer og deres salter, estere og amider
substituerte etere
substituerte arsonsyrer og deres salter, estere og amider substituerte benzimidazoler
substituerte benzisotiazoler
substituerte benztiadiazinondioksyder
substituerte benzoksaziner
substituerte benzoksazinoner
substituerte benztiadiazoler
substituerte biureter substituerte konoliner
substituerte karbamater
substituerte alifatiske karboksylsyrer og deres salter, estere og
amider
substituerte aromatiske karboksylsyrer og deres salter, estere og
amider
substituerte karbamoylalkyl-tiol- eller ditiofosfater substituerte kinazoliner
substituerte cykloalkylamidokarbontiolsiyrer og deres salter,
estere og amider
substituerte cykloalkylkarbona^mjdo-tiazoler substituerte dikarboksylsyrer og deres salter, estere og amider substituerte dihydrobenzofuranylsulfonater
substituerte disulfider
substituerte dipyridyliumsalter
substituerte ditiokafbamater
substituerte ditiofosforsyrer og deres salter, estere og amider substituerte urinstoffer
substituerte heksahydro-l-H-karbotiater
substituerte hydantoiner
substituerte hydrazider
substituerte hydrazoniumsalter
substituerte isooksazolpyrimidoner
substituerte imidazoler
substituerte isotiazolpyrimi'doner
substituerte ketoner
substituerte naftokinoner
substituerte alifatiske nitriler
substituerte aromatiske nitriler
substituerte oksadiazoler
substituerte oksadiazinoner
substituerte oksadiazolidindioner
substituerte oksadiazindioner
substituerte fenoler og deres salter og estere substituerte fosfonsyrer og deres salter, estere og amider substituerte fosfoniumklorider
substituerte fosfonalkylglyciner
substituerte fosfitter
substituerte fosforsyrer og deres salter, estere og amider substituerte piperidiner
substituerte pyrazoler
substituerte pyrazolalkylkarboksylsyrer og deres salter, estere og amider
substituerte pyrazoliumsalter
substituerte pyrazoliumalkylsulfater
substituerte pyridaziner
substituerte pyridazoner
substituerte pyridinkarboksylsyrer og deres salter, estere og
amider
substituerte pyridiner
substituerte pyridinkarboksylater
substituerte pyridinoner
substituerte pyrimidiner
substituerte pyrimidoner
substituert pyrrolidinkarboksylsyre og dennes salter, estere og
amider
substituerte pyrrolidiner
substituerte pyrrolidoner
substituerte arylsulfonsyrer og deres salter, estere og amider substituerte styrener
substituerte tetrahydro-oksadiazindioner
substituerte tetrahydro-oksadiazoldioner
substituerte tetrahydrometandXSdener
substituerte tetrahydro-diazol-tioner
substituerte tetrahydro-tiadiazin-tioner
substituerte tetrahydro-tiadiazoldioner
substituerte aromatiske tiokarboksylsyreamider substituerte tiokarboksylsyrer og deres safter, estere og!.amider substituerte tiolkarbamater
substituerte tiourinstoffer
substituerte tiofosforsyrer og deres salter, estere og amider substituerte triaziner
substituerte triazoler
substituerte uraciler
substituerte uretidindioner.
De sistnevnte herbicide forbindelser kan etter ønske anvendes før eller etter de virksomme enkeltstoffer eller blandinger
ifølge oppfinnelsen.
Tilblandingen av disse midler til herbicidene ifølge oppfinnelsen kan foretas i vektforholdet 1 : 10 til 10 : 1. Det samme gjelder for olje, fungicider, nematocider, insekticider, baktericider, motgiftmidler og vekstregulatorer.
Midlene viser en sterkt herbicid virkning og kan derfor anvendes som ugrasdrepende midler eller til bekjempelse av uønsket plantevekst. Om midlene virker som totale eller selektive midler, avhenger hovedsakelig av den mengde virksomt stoff som a'nyendes pr. flateenhet.
Med ugras og uønskede planter menes alle enfrøbladede og tofrøbladede planter som vokser på steder hvor de ikke er ønsket.
Midlene ifølge oppfinnelsen kan eksempelvis anvendes til bekjempelse av
Planter av grasfamilien, så som
De følgende forbindelser ble utprøvet i forskjellige inn-byrdes blandinger overfor de ovennevnte planter i drivhus og på friland:N-3-klor-4-metoksyfenyl-N'-metyl-N'-metoksyurinstoff N-3-klor-4-metylfenyl-N-cykloheks-l-enyl-N' , N'-dimetylurinstoff N-3-klor-4-metylfenyl-N-cykloheks-l-enyl-N•-metylurinstoff N-3-klor-4-metoksyfenyl-N-cykloheks-l-enyl-N•-metylurinstoff N-3-klor-4-metoksyfenyl-N-cykloheks-l-enyl-N', N'-dimetyl-
urinstof f
1,2-dimetyl-3,5-difenylpyrazolium-metylsulfat
1,2-dimetyl-3,5-difenylpyrazolium-p-metylfenylsulfonat Etyl-N-benzoyl-N-(3,4-diklorfenyl)-2-aminopropionat a-klor-13- (4-klorfenyl) -propionsyremetylester
N-3-klorfenylkarbaminsyre-4rklor-butin-2-yl-l-ester 3-isopropyl-2,1,3-benzotiadiazinon-(4)-2,2-dioksyd 3-isopropyl-2,1,3-benzotiadiazinon-(4)-2,2-dioksyd-natriumsalt 3-isopropyl-2,1,3-benzotiadiazinon-(4)- 2, 2-dioksyd-dimetylaminsalt
3-isopropyl-2,1,3-benzotiadiazinon-(4)-2,2-dioksyd-dietanolaminsalt
3-isopropyl-2,1,3-benzotiadiazinon-(4)-2,2-dioksyd-metylamin-salt
3-isopropyl-2,1,3-benzotiadiazinon-(4)-2,2-dioksyd-trimetyl-aminsalt
3-isopropyl-2,1,3-benzotiadiazinon-(4)-2,2-dioksyd-etylaminsalt 3-isopropyl-2,1,3-benzotiadiazinon-(4)-2,2-dioksyd-dietylaminsalt
3-isopropyl-2,1,3-benzotiadiazinon-(4)-2,2-dioksyd-etanolamin-salt
3-isoprbpy]/-2 ,1, 3-benzotiadiazinon-(4) - 2, 2-dioksyd-anilinsalt 3-isopropyl-2,1,3-benzotiadiazinon-(4)-2,2-dioksyd-pyridinsalt 3-isopropyl-2,1,3-benzotiadiazinon-(4)-2,2-dioksyd-fenylen-diaminsalt
3-isopropyl-2,1,3-benzotiadiazinon-(4)-2,2-dioksyd-cykloheksyl-aminsalt
3-isopropyl-2,1,3-benzotiadiazinon-(4)-2,2-dioksyd-dodecylheksa-metyleniminsalt
3-isopropyl-2,1,3-benzotiadiazinon-(4)- 2, 2-dioksyd-hydrazinsalt 3-siopropyl-2,1,3-benzotiadiazinon-(4)-2,2-dioksyd-magnesiumsalt 3-isopropyl-2,1,3-benzotiadiazinon-(4)-2,2-dioksyd-kalsiumsalt
3-isopropyl-2,1,3-benzotiadiazinon-(4)-2,2-dioksyd-ammoniumsalt 3-isopropyl-2,1,3-benzotiadiazinon-(4)-2,2-dioksyd-kaliumsalt 3-isopropyl-2,1,3-benzotiadiazinon-(4)-2,2-dioksyd-litiumsalt '3-isobutyl-2 ,1, 3-benzotiadiazinon-(4) -2, 2-dioksyd 3-isobutyl-2,1,3-benzotiadiazinon-(4) -2,2-dioksyd-natriumsalt 3-isobutyl-2,1,3-benzotiadiazinon-(4)-2,2-dioksyd-dimetylaminsalt
3-isobutyl-2,1,3-benzotiadiazinon-(4)-2,2-dioksyd-diétanol-amin;sa\Lt
3-sek.butyl-2,1,3-benzotiadiazinon-(4)-2,2-dioksyd 3-sek.butyl-2,1,3-benzotiadiazinon-(4)-2,2-dioksyd-natriumsalt 3-sek.butyl-2,1,3-benzotiadiazinon-(4)- 2,2-dioksyd-dimetylaminsalt
3-sek.butyl-2,1,3-benzotiadiazinon-(4)-2,2-dioksyd-dietanolaminsalt
3-n-butyl-2,1,3-benzotiadiazinon-(4)-2,2-dioksyd 3-n-butyl-2,1,3-benzotiadiazinon-(4)-2,2-dioksyd-natriumsalt 3-n-butyl-2 ,1, 3-benzotiadiazinon- (4) -2, 2-dioksy^d-dime^tylaminsalt
3-n-butyl-2,1,3-benzotiadiazinon-(4)- 2, 2-dioksyd-dietanolaminsalt
3-n-propyl-2,1,3-benzotiadiazinon-(4)-2,2-dioksyd 3-n-propyl-2,1,3-benzotiadiazinon-(4)- 2, 2-dioksyd-natriumsalt 3-n-propyl-2,1,3-benzotiadiazinon-(4)- 2, 2-dioksyd-dimetylaminsalt
3-n-propyl-2,1,3-benzotiadiazinon-(4)- 2, 2-dioksyd-dietanolaminsalt
3-etyl-2,1,3-benzotiadiazinon-(4)-2, 2-dioksyd
3-etyl-2,1,3-benzotiadiazinon-(4)- 2, 2-dioksyd-natriumsalt 3-etyl-2,1,3-benzotiadiazinon-(4)-2,2-dioksyd-dimetylaminsalt 3-etyl-2,1,3-benzotiadiazinon-(4)-2,2-dioksyd-dietanolaminsalt 3-metyl-2,1,3-benzotiadiazinon-(4)- 2, 2-dioksyd 3-metyl-2,1,3-benzotiadiazinon-(4)-2,2-dioksyd-natriumsalt 3-metyl-2,1,3-benzotiadiazinon-(4)-2,2-dioksyd-dimetylaminsalt 3-metyl-2,1,3-benzotiadiazinon-(4)-2,2-dioksyd-dietanolaminsalt
a-(2-metyl-4-klorfenoksy)-propionsyre-natriumsalt a-(2-metyl-4-klorfenoksy)-propionsyre-dimetylaminsalt a- (2-metyl-4-klorfenoksyr) -propionsyre-dietanolaminsalt -(2-metyl-4-klorfenoksy)-smøsrsyre-dimetylaminsalt a -(2,4-diklorfenoksy)-propionsyre-natriumsalt a-(2,4-diklorfenoksy)-propionsyre-dimetylaminsalt a-(2,4-diklorfenoksy)-propionsyre-dietanolaminsalt a- (2,4-diklorfenoksy)-propionsyre-isooktylester «-(2,4,5-triklorfenoksy)-propionsyre-kaliumsalt a-(2,4,5-triklorfenoksy)-propionsyre-dietylaminsalt a-(2,4y5-triklorfenoksy)-propionsyre-amylester a-(2,4,5-triklorfenoksy)-propionsyre-isooktylester a-(2-klorfenoksy)-propionsyre-dimetylarainsalt a-(4-klorfenoksy)-propionsyre-dimetylaminsalt a-(2-metylfenoksy)-propionsyre-dimetylaminsalt a-(2-metylfenoksy)-propionsyre-natriumsalt a-(2-metylfenoksy)-propionsyre-isooktylester ^-(2,4-diklorfenoksy)-smørsyre-natriumsalt ^- (2,4-diklorfe<n>oksy)-smørsyre-dimetylaminsalt ^- (2,4-diklorfenoksy)-smørsyre-dietanolaminsalt (q/-(2/ 4-diklorfenoksy) -smørsyre-isooktylester ^-(2-klorfenoksy)-smørsyre-dimetylaminsalt 2-klorfenoksyeddiksyre-dimetylaminsalt 4-klorfenoksyeddiksyre-dimetylaminsalt 2,4,5-triklorfenoksyeddiksyre-kaliumsalt 2,4,5-triklorfenoksyeddiksyre-dietylaminsalt 2,4,5-triklorfenoksyeddiksyre-amylester 2,4-diklorfenoksyeddiksyre-natriumsalt 2,4-diklorfenoksyeddiksyre-dimetylaminsalt 2,4-diklorfenoksyeddiksyre-dietanolaminsalt 2,4-diklorfenoksyeddiksyre-isooktylester 2-metyl-4-klorfenoksy-eddiksyre-natriumsalt 2-metyl-4-klorfenoksy-eddiksyre-dimetylaminsalt 2-metyl-4-klorfenoksy-eddiksyre-dietanolaminsalt y~ (2-metyl-4-klorfenoksy)-smørsyre-natriumsalt 2f- (2,4, 5-triklorfenoksy) -smørsyre-dimetylaminsalt.
Blandingene har en tilsvarende biologisk virkning som d lene 1-4 angitte blandinger.
Eksempel 1
På friland ble forskjellige planter ved en veksthøyde på 2-20 cm behandlet med de følgende virksomme enkeltstoffer og deres blandinger i form av dispersjoner:
I l-m-klor-p-metoksyfenyl-3-metyl-3-metoksyurinstoff
II a-(2,4-diklorfenoksy)-propionsyre-dimetylaminsalt
III etyl-N-benzoyl-N-(3,4-diklorfenyl)-2-aminopropionat
IV 1,2-dimetyl-difenyl-pyrazolium-metylsulfat
VI a-klor-S-(4-klorfenyl)-propionsyre-metylester
i hvert tilfelle 0,25 -0,5 - 1 - 1,5 - 2 og 4 kg/ha aktivt stoff.
I+II+III, I+II+IV, I+II+V, I+II+VI i hvert tilfelle 0,5+0,5+1;
0,5+1+0,5?1+0,5+0,5; 0,25+0,25+1,5; 0,25+1,5+0,25;
1,5+0,25+0,25; 1+1+2; 1+2+1; 2+1+1 kg/ha aktivt stoff.
Etter 12-16 dager ble det slått fast at blandingene viste en bedre herbicid virkning ved samme forenlighet med kulturplantene enn enkeltstoffene.
Forsøksresultatet vil fremgå av den følgende tabell.
Eksempel 2
På friland ble forskjellige planter ved en veksthøyde på 2-22 cm behandlet med de følgende virksomme enkeltstoffer og deres blandinger i form av dispersjoner*
I l-m-klor-p-metoksyfenyl-3-metyl-3-metoksyurinstoff
III etyl-N-benzoyl-N-(3,4-diklorfenyl)-2-aminopropionat
IV 1,2-dimetyl-difenyl-pyrazolium-metylsulfat
V N-3-klorfenyl-karbaminsyre-4-klor-butin-2-yl-l-ester
VI a-klor-S-(4-klorfenyl)-propionsyre-metylester
VII 3-isopropyl-2,1,3-benzotiadiazinon-(4)-2,2-dioksyd
i hvertllililfelle 0,25 - 0,5 - 1 - 1,5 - 2 og 4 kg/ha aktivt stoff
I+VII+III, I+VII+IV, I+VII+V, I+VII+VI i hvert tilfelle 0,5+0,5+1;
0,5+1+0,75; 1+0,5+0,5; 0,25+0,25+1,5; 0,25+1,5+0,25;
1,5+0,25+0,25; 1+1+2; 1+2+1; 2+1+1 kg/ha aktivt stoff.
Etter 12-15 dager ble det slått fast at blandingene viste en bedre herbicici virkning ved samme forenlighet med kulturplantene enn enkeltstoffene.
Forsøksresultatet vil fremgå av den følgende tabell.
Eksempel 3
I et drivhus ble forskjellige planter ved en veksthøyde på 2-22 cm behandlet med de følgende virksomme enkeltstoffer og deres blandinger (emulsjon-dispersjon-tankblanding)•
IX lTrklor-4-metylfenyl-N-cykloheks-l-enyl-N' 7?^' -dimetyl-urinstoff
VIII 3-isopropyl-2,1,3-benzotiadiazinon-(4)-2,2-dioksyd-natriumsalt
III Etyl-N-benzoyl-N-(3,4-diklorfenyl)-2-aminopropionat
IV 1,2-dimetyl-difenyl-pyrazol'ium-metylsulfat
V N-3-klorfenyl-karbaminsyre-4-klor-butin-2-yl-l-ester
VI a-klor-8-(4-klorfenyl)-propionsyre-matylester
i hvert tilfelle 0,25 - 0,5 - 1 - 1,5 - 2 og 4 kg/ha
aktivt stoff
IX+VIII+III, IX+VIII+IV, IX+VIII+V, IX+VIII+VI,
i hvert tilfelle 0,5+0,5+1; 0,5+1+0,5; 1+0, 5+0, 5;f~] 0,25+0,25+1,5; 0,25+1,5+0,25; 1,5+0,25+0,25; 1+1+2;
1+2+1; 2+1+1 kg/ha aktivt stoff.
Etter 12-15 dager ble det slått fast at blandingene viste en bedre herbicid virkning ved samme forenlighet med kulturplantene enn enkeltstoffene.
Forsøksresultatet vil fremgå av den følgende tabell.
Eksempel 4
I et drivhus ble forskjellige planter ved en veksthøyde på 2-20 cm behandlet med de følgende virksomme enkeltstoffer og deres blandinger i, form av pasta*
IX 3-klor-4-metylfenyl-N-cykloheks-l-enyl-N',N *-dimetyl-urinstoff
II a-(2,4-diklorfenpksy)-propionsyre-dimetylaminsalt
III Etyl-N-benzoyl-N^(3,4-diklorfenyl)-2-aminopropionat
IV 1,2-dimetyl-difenyl-pyrazolium-metylsulfat
V N-3-klorfenyl-karbaminsyre-4-klor-butin-2-yl-l-ester
VI a-klor-6-(4-klorfenyl)-propionsyre-metylester
i hvert tilfelle 0,25 - o;,5^- 1 - 1,5 - 2 og 4 kg/ha aktivt stoff
IX+II+III, IX+II+IV, IX+II+V, IX+II+VI i hvert tilfelle 0,5+0,5+1; p;
0,5+1+0,5; 1+0,5+0,5; 0,25+0,25+1,5; 0,25+1,5+0,25;
1,5+0,25+0,25; 1+1+2; 1+2+1; 2+1+1 kg/ha aktivt stoff.
Etter 12-16 dager ble det slått fast at blandingene viste en bedre herbicid virkning ved samme forenlighet med kulturplantene enn enkeltstoffene.
Forsøksresultatet vil fremgå av den følgende tabell.
Claims (1)
- H erbicid, karakterisert ved at det inneholder en blanding ava) en forbindelse med formellenhvor x bejtyr metoksy når betyr metoksy og R betyr hydrogen, og X betyr metyl, metoksy eller halogen når R betyr.en cykloalkylrest og R^ betyr metyl, hydrogen eller metoksy, og/ellerb) en forbindelse med formelenhvor R betyr alkyloksy eller en eventuelt med halogen eller metyl substituert fenylrest, og/ellerc) forbindelsenog/eller d) forbindelsen og/eller e) forbindelsenog/ellerf) en forbindelse med formelenhvor R betyr lavere alkyl, R^ betyr hydrogen eller sal- tene, og/ellerg) en forbindelse med formelenhvor X betyr halogen eller metyl, R betyr hydrogen eller alkyl,n har verdier fra 0 til 3, m har verdier fra 0 til 2, R^ betyr alkyl, hydrogen eller saltene.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19732333414 DE2333414A1 (de) | 1973-06-30 | 1973-06-30 | Herbizid |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| NO741906L true NO741906L (no) | 1975-01-27 |
Family
ID=5885621
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO741906A NO741906L (no) | 1973-06-30 | 1974-05-24 |
Country Status (13)
| Country | Link |
|---|---|
| JP (1) | JPS5036635A (no) |
| AU (1) | AU6979674A (no) |
| BE (1) | BE817008A (no) |
| BR (1) | BR7405169D0 (no) |
| DD (1) | DD111779A5 (no) |
| DE (1) | DE2333414A1 (no) |
| DK (1) | DK327174A (no) |
| FR (1) | FR2234862A1 (no) |
| IL (1) | IL44976A0 (no) |
| LU (1) | LU70437A1 (no) |
| NL (1) | NL7408692A (no) |
| NO (1) | NO741906L (no) |
| SE (1) | SE7408582L (no) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1546375A (en) * | 1975-04-30 | 1979-05-23 | Shell Int Research | Wild oat herbicide |
-
1973
- 1973-06-30 DE DE19732333414 patent/DE2333414A1/de active Pending
-
1974
- 1974-05-24 NO NO741906A patent/NO741906L/no unknown
- 1974-06-05 AU AU69796/74A patent/AU6979674A/en not_active Expired
- 1974-06-05 IL IL44976A patent/IL44976A0/xx unknown
- 1974-06-19 JP JP49069264A patent/JPS5036635A/ja active Pending
- 1974-06-19 DK DK327174A patent/DK327174A/da unknown
- 1974-06-25 BR BR5169/74A patent/BR7405169D0/pt unknown
- 1974-06-26 FR FR7422203A patent/FR2234862A1/fr active Pending
- 1974-06-27 NL NL7408692A patent/NL7408692A/xx unknown
- 1974-06-28 LU LU70437A patent/LU70437A1/xx unknown
- 1974-06-28 BE BE146006A patent/BE817008A/xx unknown
- 1974-06-28 SE SE7408582A patent/SE7408582L/xx not_active Application Discontinuation
- 1974-06-28 DD DD179581A patent/DD111779A5/xx unknown
Also Published As
| Publication number | Publication date |
|---|---|
| FR2234862A1 (en) | 1975-01-24 |
| DE2333414A1 (de) | 1975-01-16 |
| BR7405169D0 (pt) | 1975-01-07 |
| IL44976A0 (en) | 1974-09-10 |
| NL7408692A (nl) | 1975-01-02 |
| SE7408582L (no) | 1975-01-02 |
| DK327174A (no) | 1975-02-10 |
| LU70437A1 (no) | 1974-10-17 |
| DD111779A5 (no) | 1975-03-12 |
| AU6979674A (en) | 1975-12-11 |
| BE817008A (fr) | 1974-12-30 |
| JPS5036635A (no) | 1975-04-05 |
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