CN1758850A - 包含Picolinafen的除草混合物 - Google Patents
包含Picolinafen的除草混合物 Download PDFInfo
- Publication number
- CN1758850A CN1758850A CNA2004800067646A CN200480006764A CN1758850A CN 1758850 A CN1758850 A CN 1758850A CN A2004800067646 A CNA2004800067646 A CN A2004800067646A CN 200480006764 A CN200480006764 A CN 200480006764A CN 1758850 A CN1758850 A CN 1758850A
- Authority
- CN
- China
- Prior art keywords
- component
- class
- acid
- page
- picolinafen
- Prior art date
- Legal status (The legal status 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 status listed.)
- Pending
Links
- 230000002363 herbicidal effect Effects 0.000 title claims abstract description 66
- 239000000203 mixture Substances 0.000 title claims abstract description 65
- CWKFPEBMTGKLKX-UHFFFAOYSA-N picolinafen Chemical compound C1=CC(F)=CC=C1NC(=O)C1=CC=CC(OC=2C=C(C=CC=2)C(F)(F)F)=N1 CWKFPEBMTGKLKX-UHFFFAOYSA-N 0.000 title claims abstract description 42
- 239000005596 Picolinafen Substances 0.000 title claims abstract description 40
- 239000004009 herbicide Substances 0.000 claims abstract description 59
- 150000003839 salts Chemical class 0.000 claims abstract description 32
- 150000001408 amides Chemical class 0.000 claims abstract description 15
- 150000003936 benzamides Chemical class 0.000 claims abstract description 15
- 229940054066 benzamide antipsychotics Drugs 0.000 claims abstract description 12
- 235000010233 benzoic acid Nutrition 0.000 claims abstract description 11
- 150000001559 benzoic acids Chemical class 0.000 claims abstract description 11
- LOAUVZALPPNFOQ-UHFFFAOYSA-N quinaldic acid Chemical class C1=CC=CC2=NC(C(=O)O)=CC=C21 LOAUVZALPPNFOQ-UHFFFAOYSA-N 0.000 claims abstract description 11
- AAILEWXSEQLMNI-UHFFFAOYSA-N 1h-pyridazin-6-one Chemical class OC1=CC=CN=N1 AAILEWXSEQLMNI-UHFFFAOYSA-N 0.000 claims abstract description 9
- MHKBMNACOMRIAW-UHFFFAOYSA-N 2,3-dinitrophenol Chemical class OC1=CC=CC([N+]([O-])=O)=C1[N+]([O-])=O MHKBMNACOMRIAW-UHFFFAOYSA-N 0.000 claims abstract description 9
- 150000004657 carbamic acid derivatives Chemical class 0.000 claims abstract description 8
- 150000002825 nitriles Chemical class 0.000 claims abstract description 8
- 150000004892 pyridazines Chemical class 0.000 claims abstract description 8
- 150000007659 semicarbazones Chemical class 0.000 claims abstract description 8
- -1 phthalamic acid ester Chemical class 0.000 claims description 63
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims description 54
- 150000001875 compounds Chemical class 0.000 claims description 34
- YTPLMLYBLZKORZ-UHFFFAOYSA-N Thiophene Chemical compound C=1C=CSC=1 YTPLMLYBLZKORZ-UHFFFAOYSA-N 0.000 claims description 26
- YZHUMGUJCQRKBT-UHFFFAOYSA-M sodium chlorate Chemical compound [Na+].[O-]Cl(=O)=O YZHUMGUJCQRKBT-UHFFFAOYSA-M 0.000 claims description 24
- 241000196324 Embryophyta Species 0.000 claims description 23
- 150000002148 esters Chemical class 0.000 claims description 22
- 244000025254 Cannabis sativa Species 0.000 claims description 21
- LPXYXBZAXFTFKH-UHFFFAOYSA-N ClC=1C(=C(C(=NC1)C(=O)O)C(=O)O)Cl Chemical compound ClC=1C(=C(C(=NC1)C(=O)O)C(=O)O)Cl LPXYXBZAXFTFKH-UHFFFAOYSA-N 0.000 claims description 20
- 239000005504 Dicamba Substances 0.000 claims description 20
- IWEDIXLBFLAXBO-UHFFFAOYSA-N dicamba Chemical compound COC1=C(Cl)C=CC(Cl)=C1C(O)=O IWEDIXLBFLAXBO-UHFFFAOYSA-N 0.000 claims description 20
- 238000000034 method Methods 0.000 claims description 19
- ISAKRJDGNUQOIC-UHFFFAOYSA-N Uracil Chemical compound O=C1C=CNC(=O)N1 ISAKRJDGNUQOIC-UHFFFAOYSA-N 0.000 claims description 18
- ZOMSMJKLGFBRBS-UHFFFAOYSA-N bentazone Chemical compound C1=CC=C2NS(=O)(=O)N(C(C)C)C(=O)C2=C1 ZOMSMJKLGFBRBS-UHFFFAOYSA-N 0.000 claims description 18
- 239000005570 Isoxaben Substances 0.000 claims description 16
- PMHURSZHKKJGBM-UHFFFAOYSA-N isoxaben Chemical compound O1N=C(C(C)(CC)CC)C=C1NC(=O)C1=C(OC)C=CC=C1OC PMHURSZHKKJGBM-UHFFFAOYSA-N 0.000 claims description 16
- 150000003233 pyrroles Chemical class 0.000 claims description 16
- 150000007970 thio esters Chemical class 0.000 claims description 16
- FIKAKWIAUPDISJ-UHFFFAOYSA-L paraquat dichloride Chemical compound [Cl-].[Cl-].C1=C[N+](C)=CC=C1C1=CC=[N+](C)C=C1 FIKAKWIAUPDISJ-UHFFFAOYSA-L 0.000 claims description 15
- OWZPCEFYPSAJFR-UHFFFAOYSA-N 2-(butan-2-yl)-4,6-dinitrophenol Chemical compound CCC(C)C1=CC([N+]([O-])=O)=CC([N+]([O-])=O)=C1O OWZPCEFYPSAJFR-UHFFFAOYSA-N 0.000 claims description 14
- 239000005594 Phenmedipham Substances 0.000 claims description 14
- 239000005608 Quinmerac Substances 0.000 claims description 14
- IDOWTHOLJBTAFI-UHFFFAOYSA-N phenmedipham Chemical compound COC(=O)NC1=CC=CC(OC(=O)NC=2C=C(C)C=CC=2)=C1 IDOWTHOLJBTAFI-UHFFFAOYSA-N 0.000 claims description 14
- ALZOLUNSQWINIR-UHFFFAOYSA-N quinmerac Chemical compound OC(=O)C1=C(Cl)C=CC2=CC(C)=CN=C21 ALZOLUNSQWINIR-UHFFFAOYSA-N 0.000 claims description 14
- PSYBGEADHLUXCS-UHFFFAOYSA-N Isocil Chemical compound CC(C)N1C(=O)NC(C)=C(Br)C1=O PSYBGEADHLUXCS-UHFFFAOYSA-N 0.000 claims description 13
- 150000001412 amines Chemical class 0.000 claims description 13
- 229930192474 thiophene Natural products 0.000 claims description 13
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 12
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 11
- ICJSJAJWTWPSBD-UHFFFAOYSA-N cloquintocet Chemical compound C1=CN=C2C(OCC(=O)O)=CC=C(Cl)C2=C1 ICJSJAJWTWPSBD-UHFFFAOYSA-N 0.000 claims description 11
- OBISXEJSEGNNKL-UHFFFAOYSA-N dinitrogen-n-sulfide Chemical class [N-]=[N+]=S OBISXEJSEGNNKL-UHFFFAOYSA-N 0.000 claims description 10
- HSSBORCLYSCBJR-UHFFFAOYSA-N Chloramben Chemical compound NC1=CC(Cl)=CC(C(O)=O)=C1Cl HSSBORCLYSCBJR-UHFFFAOYSA-N 0.000 claims description 9
- 241000234653 Cyperus Species 0.000 claims description 9
- 239000005630 Diquat Substances 0.000 claims description 9
- SYJFEGQWDCRVNX-UHFFFAOYSA-N diquat Chemical compound C1=CC=[N+]2CC[N+]3=CC=CC=C3C2=C1 SYJFEGQWDCRVNX-UHFFFAOYSA-N 0.000 claims description 9
- ITGSCCPVERXFGN-UHFFFAOYSA-N isoxadifen Chemical group C1C(C(=O)O)=NOC1(C=1C=CC=CC=1)C1=CC=CC=C1 ITGSCCPVERXFGN-UHFFFAOYSA-N 0.000 claims description 9
- 229940035893 uracil Drugs 0.000 claims description 9
- 239000005572 Lenacil Substances 0.000 claims description 8
- ZTMKADLOSYKWCA-UHFFFAOYSA-N lenacil Chemical compound O=C1NC=2CCCC=2C(=O)N1C1CCCCC1 ZTMKADLOSYKWCA-UHFFFAOYSA-N 0.000 claims description 8
- 239000007787 solid Substances 0.000 claims description 8
- UXPRZZZNGFVXRR-UHFFFAOYSA-N 2,3-difluoro-1h-pyrrole Chemical compound FC=1C=CNC=1F UXPRZZZNGFVXRR-UHFFFAOYSA-N 0.000 claims description 7
- UDRNNGBAXFCBLJ-UHFFFAOYSA-N 2-chloro-n-(2,3-dimethylphenyl)-n-propan-2-ylacetamide Chemical compound ClCC(=O)N(C(C)C)C1=CC=CC(C)=C1C UDRNNGBAXFCBLJ-UHFFFAOYSA-N 0.000 claims description 7
- CTSLUCNDVMMDHG-UHFFFAOYSA-N 5-bromo-3-(butan-2-yl)-6-methylpyrimidine-2,4(1H,3H)-dione Chemical compound CCC(C)N1C(=O)NC(C)=C(Br)C1=O CTSLUCNDVMMDHG-UHFFFAOYSA-N 0.000 claims description 7
- VTNQPKFIQCLBDU-UHFFFAOYSA-N Acetochlor Chemical compound CCOCN(C(=O)CCl)C1=C(C)C=CC=C1CC VTNQPKFIQCLBDU-UHFFFAOYSA-N 0.000 claims description 7
- MDBGGTQNNUOQRC-UHFFFAOYSA-N Allidochlor Chemical compound ClCC(=O)N(CC=C)CC=C MDBGGTQNNUOQRC-UHFFFAOYSA-N 0.000 claims description 7
- XTFNPKDYCLFGPV-OMCISZLKSA-N Bromofenoxim Chemical compound C1=C(Br)C(O)=C(Br)C=C1\C=N\OC1=CC=C([N+]([O-])=O)C=C1[N+]([O-])=O XTFNPKDYCLFGPV-OMCISZLKSA-N 0.000 claims description 7
- 239000005490 Carbetamide Substances 0.000 claims description 7
- 239000005493 Chloridazon (aka pyrazone) Substances 0.000 claims description 7
- 239000005647 Chlorpropham Substances 0.000 claims description 7
- QAHFOPIILNICLA-UHFFFAOYSA-N Diphenamid Chemical compound C=1C=CC=CC=1C(C(=O)N(C)C)C1=CC=CC=C1 QAHFOPIILNICLA-UHFFFAOYSA-N 0.000 claims description 7
- KXGYBSNVFXBPNO-UHFFFAOYSA-N Monalide Chemical compound CCCC(C)(C)C(=O)NC1=CC=C(Cl)C=C1 KXGYBSNVFXBPNO-UHFFFAOYSA-N 0.000 claims description 7
- NBQCNZYJJMBDKY-UHFFFAOYSA-N Terbacil Chemical compound CC=1NC(=O)N(C(C)(C)C)C(=O)C=1Cl NBQCNZYJJMBDKY-UHFFFAOYSA-N 0.000 claims description 7
- AMRQXHFXNZFDCH-SECBINFHSA-N [(2r)-1-(ethylamino)-1-oxopropan-2-yl] n-phenylcarbamate Chemical compound CCNC(=O)[C@@H](C)OC(=O)NC1=CC=CC=C1 AMRQXHFXNZFDCH-SECBINFHSA-N 0.000 claims description 7
- QLULGSLAHXLKSR-UHFFFAOYSA-N azane;phosphane Chemical compound N.P QLULGSLAHXLKSR-UHFFFAOYSA-N 0.000 claims description 7
- 235000010290 biphenyl Nutrition 0.000 claims description 7
- 125000006267 biphenyl group Chemical group 0.000 claims description 7
- WYKYKTKDBLFHCY-UHFFFAOYSA-N chloridazon Chemical compound O=C1C(Cl)=C(N)C=NN1C1=CC=CC=C1 WYKYKTKDBLFHCY-UHFFFAOYSA-N 0.000 claims description 7
- CWJSHJJYOPWUGX-UHFFFAOYSA-N chlorpropham Chemical compound CC(C)OC(=O)NC1=CC=CC(Cl)=C1 CWJSHJJYOPWUGX-UHFFFAOYSA-N 0.000 claims description 7
- DGPBHERUGBOSFZ-UHFFFAOYSA-N n-but-3-yn-2-yl-2-chloro-n-phenylacetamide Chemical compound C#CC(C)N(C(=O)CCl)C1=CC=CC=C1 DGPBHERUGBOSFZ-UHFFFAOYSA-N 0.000 claims description 7
- VXPLXMJHHKHSOA-UHFFFAOYSA-N propham Chemical compound CC(C)OC(=O)NC1=CC=CC=C1 VXPLXMJHHKHSOA-UHFFFAOYSA-N 0.000 claims description 7
- PHNUZKMIPFFYSO-UHFFFAOYSA-N propyzamide Chemical compound C#CC(C)(C)NC(=O)C1=CC(Cl)=CC(Cl)=C1 PHNUZKMIPFFYSO-UHFFFAOYSA-N 0.000 claims description 7
- RDJTWDKSYLLHRW-UHFFFAOYSA-N Dinoseb acetate Chemical compound CCC(C)C1=CC([N+]([O-])=O)=CC([N+]([O-])=O)=C1OC(C)=O RDJTWDKSYLLHRW-UHFFFAOYSA-N 0.000 claims description 6
- YUBJPYNSGLJZPQ-UHFFFAOYSA-N Dithiopyr Chemical compound CSC(=O)C1=C(C(F)F)N=C(C(F)(F)F)C(C(=O)SC)=C1CC(C)C YUBJPYNSGLJZPQ-UHFFFAOYSA-N 0.000 claims description 6
- 239000005580 Metazachlor Substances 0.000 claims description 6
- XCSGPAVHZFQHGE-UHFFFAOYSA-N alachlor Chemical compound CCC1=CC=CC(CC)=C1N(COC)C(=O)CCl XCSGPAVHZFQHGE-UHFFFAOYSA-N 0.000 claims description 6
- VGPYEHKOIGNJKV-UHFFFAOYSA-N asulam Chemical compound COC(=O)NS(=O)(=O)C1=CC=C(N)C=C1 VGPYEHKOIGNJKV-UHFFFAOYSA-N 0.000 claims description 6
- 239000004305 biphenyl Substances 0.000 claims description 6
- WZDDLAZXUYIVMU-UHFFFAOYSA-N bromobutide Chemical compound CC(C)(C)C(Br)C(=O)NC(C)(C)C1=CC=CC=C1 WZDDLAZXUYIVMU-UHFFFAOYSA-N 0.000 claims description 6
- HKPHPIREJKHECO-UHFFFAOYSA-N butachlor Chemical compound CCCCOCN(C(=O)CCl)C1=C(CC)C=CC=C1CC HKPHPIREJKHECO-UHFFFAOYSA-N 0.000 claims description 6
- STEPQTYSZVCJPV-UHFFFAOYSA-N metazachlor Chemical compound CC1=CC=CC(C)=C1N(C(=O)CCl)CN1N=CC=C1 STEPQTYSZVCJPV-UHFFFAOYSA-N 0.000 claims description 6
- JYNOTRFRRIKTHZ-UHFFFAOYSA-N n-(2-tert-butyl-6-methylphenyl)-2-chloroacetamide Chemical compound CC1=CC=CC(C(C)(C)C)=C1NC(=O)CCl JYNOTRFRRIKTHZ-UHFFFAOYSA-N 0.000 claims description 6
- HZDIJTXDRLNTIS-DAXSKMNVSA-N n-[[(z)-but-2-enoxy]methyl]-2-chloro-n-(2,6-diethylphenyl)acetamide Chemical compound CCC1=CC=CC(CC)=C1N(COC\C=C/C)C(=O)CCl HZDIJTXDRLNTIS-DAXSKMNVSA-N 0.000 claims description 6
- JXTHEWSKYLZVJC-UHFFFAOYSA-N naptalam Chemical compound OC(=O)C1=CC=CC=C1C(=O)NC1=CC=CC2=CC=CC=C12 JXTHEWSKYLZVJC-UHFFFAOYSA-N 0.000 claims description 6
- LLLFASISUZUJEQ-UHFFFAOYSA-N orbencarb Chemical compound CCN(CC)C(=O)SCC1=CC=CC=C1Cl LLLFASISUZUJEQ-UHFFFAOYSA-N 0.000 claims description 6
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 claims description 6
- MFOUDYKPLGXPGO-UHFFFAOYSA-N propachlor Chemical compound ClCC(=O)N(C(C)C)C1=CC=CC=C1 MFOUDYKPLGXPGO-UHFFFAOYSA-N 0.000 claims description 6
- 239000004094 surface-active agent Substances 0.000 claims description 5
- 244000038559 crop plants Species 0.000 claims description 3
- 230000008569 process Effects 0.000 claims description 2
- 239000012530 fluid Substances 0.000 claims 2
- 150000001735 carboxylic acids Chemical class 0.000 claims 1
- FNQJDLTXOVEEFB-UHFFFAOYSA-N 1,2,3-benzothiadiazole Chemical class C1=CC=C2SN=NC2=C1 FNQJDLTXOVEEFB-UHFFFAOYSA-N 0.000 abstract 1
- VONWPEXRCLHKRJ-UHFFFAOYSA-N 2-chloro-n-phenylacetamide Chemical class ClCC(=O)NC1=CC=CC=C1 VONWPEXRCLHKRJ-UHFFFAOYSA-N 0.000 abstract 1
- BSCCSDNZEIHXOK-UHFFFAOYSA-N phenyl carbamate Chemical class NC(=O)OC1=CC=CC=C1 BSCCSDNZEIHXOK-UHFFFAOYSA-N 0.000 abstract 1
- 230000000694 effects Effects 0.000 description 17
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 12
- 239000012948 isocyanate Substances 0.000 description 12
- 239000002253 acid Substances 0.000 description 9
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 9
- HIXDQWDOVZUNNA-UHFFFAOYSA-N 2-(3,4-dimethoxyphenyl)-5-hydroxy-7-methoxychromen-4-one Chemical compound C=1C(OC)=CC(O)=C(C(C=2)=O)C=1OC=2C1=CC=C(OC)C(OC)=C1 HIXDQWDOVZUNNA-UHFFFAOYSA-N 0.000 description 8
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical class CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 7
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Natural products OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 7
- FLKPEMZONWLCSK-UHFFFAOYSA-N diethyl phthalate Chemical class CCOC(=O)C1=CC=CC=C1C(=O)OCC FLKPEMZONWLCSK-UHFFFAOYSA-N 0.000 description 7
- MWKVXOJATACCCH-UHFFFAOYSA-N isoxadifen-ethyl Chemical group C1C(C(=O)OCC)=NOC1(C=1C=CC=CC=1)C1=CC=CC=C1 MWKVXOJATACCCH-UHFFFAOYSA-N 0.000 description 7
- ROSDSFDQCJNGOL-UHFFFAOYSA-N Dimethylamine Chemical compound CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 description 6
- 239000003921 oil Substances 0.000 description 6
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 5
- 239000000843 powder Substances 0.000 description 5
- 230000002195 synergetic effect Effects 0.000 description 5
- 241000335053 Beta vulgaris Species 0.000 description 4
- 240000007154 Coffea arabica Species 0.000 description 4
- 239000013543 active substance Substances 0.000 description 4
- QGZKDVFQNNGYKY-UHFFFAOYSA-O ammonium group Chemical group [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 4
- 239000012141 concentrate Substances 0.000 description 4
- 239000002245 particle Substances 0.000 description 4
- 239000000725 suspension Substances 0.000 description 4
- 238000012360 testing method Methods 0.000 description 4
- 238000009333 weeding Methods 0.000 description 4
- QRNATDQRFAUDKF-UHFFFAOYSA-N 2-carbamothioylsulfanylethyl carbamodithioate Chemical compound NC(=S)SCCSC(N)=S QRNATDQRFAUDKF-UHFFFAOYSA-N 0.000 description 3
- 235000010469 Glycine max Nutrition 0.000 description 3
- 244000068988 Glycine max Species 0.000 description 3
- 244000299507 Gossypium hirsutum Species 0.000 description 3
- 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 3
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- ZRKWMRDKSOPRRS-UHFFFAOYSA-N N-Methyl-N-nitrosourea Chemical class O=NN(C)C(N)=O ZRKWMRDKSOPRRS-UHFFFAOYSA-N 0.000 description 3
- 240000007594 Oryza sativa Species 0.000 description 3
- 244000046052 Phaseolus vulgaris Species 0.000 description 3
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
- 240000008042 Zea mays Species 0.000 description 3
- ZXVOCOLRQJZVBW-UHFFFAOYSA-N azane;ethanol Chemical compound N.CCO ZXVOCOLRQJZVBW-UHFFFAOYSA-N 0.000 description 3
- 125000006226 butoxyethyl group Chemical group 0.000 description 3
- 235000013339 cereals Nutrition 0.000 description 3
- 239000007859 condensation product Substances 0.000 description 3
- 239000000839 emulsion Substances 0.000 description 3
- 125000005448 ethoxyethyl group Chemical group [H]C([H])([H])C([H])([H])OC([H])([H])C([H])([H])* 0.000 description 3
- 150000002191 fatty alcohols Chemical class 0.000 description 3
- JJWLVOIRVHMVIS-UHFFFAOYSA-O isopropylaminium Chemical compound CC(C)[NH3+] JJWLVOIRVHMVIS-UHFFFAOYSA-O 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 229910052749 magnesium Inorganic materials 0.000 description 3
- 239000011777 magnesium Substances 0.000 description 3
- 239000006072 paste Substances 0.000 description 3
- 229920000151 polyglycol Polymers 0.000 description 3
- 239000010695 polyglycol Substances 0.000 description 3
- 229910052700 potassium Inorganic materials 0.000 description 3
- 239000011591 potassium Substances 0.000 description 3
- 229910052708 sodium Inorganic materials 0.000 description 3
- 239000011734 sodium Substances 0.000 description 3
- 238000009331 sowing Methods 0.000 description 3
- 239000007921 spray Substances 0.000 description 3
- 238000005507 spraying Methods 0.000 description 3
- GETQZCLCWQTVFV-UHFFFAOYSA-N trimethylamine Chemical compound CN(C)C GETQZCLCWQTVFV-UHFFFAOYSA-N 0.000 description 3
- NRZWQKGABZFFKE-UHFFFAOYSA-N trimethylsulfonium Chemical compound C[S+](C)C NRZWQKGABZFFKE-UHFFFAOYSA-N 0.000 description 3
- 244000291564 Allium cepa Species 0.000 description 2
- 244000099147 Ananas comosus Species 0.000 description 2
- 235000007119 Ananas comosus Nutrition 0.000 description 2
- 244000105624 Arachis hypogaea Species 0.000 description 2
- 235000010777 Arachis hypogaea Nutrition 0.000 description 2
- 244000003416 Asparagus officinalis Species 0.000 description 2
- 235000005340 Asparagus officinalis Nutrition 0.000 description 2
- 235000016068 Berberis vulgaris Nutrition 0.000 description 2
- 235000021533 Beta vulgaris Nutrition 0.000 description 2
- 235000006008 Brassica napus var napus Nutrition 0.000 description 2
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 2
- 235000003255 Carthamus tinctorius Nutrition 0.000 description 2
- 244000020518 Carthamus tinctorius Species 0.000 description 2
- 244000068645 Carya illinoensis Species 0.000 description 2
- 235000009025 Carya illinoensis Nutrition 0.000 description 2
- 235000005979 Citrus limon Nutrition 0.000 description 2
- 244000131522 Citrus pyriformis Species 0.000 description 2
- 235000005976 Citrus sinensis Nutrition 0.000 description 2
- 240000002319 Citrus sinensis Species 0.000 description 2
- 240000008067 Cucumis sativus Species 0.000 description 2
- 244000052363 Cynodon dactylon Species 0.000 description 2
- 235000001950 Elaeis guineensis Nutrition 0.000 description 2
- QUSNBJAOOMFDIB-UHFFFAOYSA-N Ethylamine Chemical class CCN QUSNBJAOOMFDIB-UHFFFAOYSA-N 0.000 description 2
- 235000014751 Gossypium arboreum Nutrition 0.000 description 2
- 235000009429 Gossypium barbadense Nutrition 0.000 description 2
- 244000020551 Helianthus annuus Species 0.000 description 2
- 235000003222 Helianthus annuus Nutrition 0.000 description 2
- 240000005979 Hordeum vulgare Species 0.000 description 2
- 235000007340 Hordeum vulgare Nutrition 0.000 description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
- 244000017020 Ipomoea batatas Species 0.000 description 2
- 235000002678 Ipomoea batatas Nutrition 0.000 description 2
- 240000007049 Juglans regia Species 0.000 description 2
- 235000009496 Juglans regia Nutrition 0.000 description 2
- 240000004322 Lens culinaris Species 0.000 description 2
- 235000010666 Lens esculenta Nutrition 0.000 description 2
- 235000004431 Linum usitatissimum Nutrition 0.000 description 2
- 240000006240 Linum usitatissimum Species 0.000 description 2
- 235000007688 Lycopersicon esculentum Nutrition 0.000 description 2
- CPLXHLVBOLITMK-UHFFFAOYSA-N Magnesium oxide Chemical compound [Mg]=O CPLXHLVBOLITMK-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
- 241000220225 Malus Species 0.000 description 2
- 235000010624 Medicago sativa Nutrition 0.000 description 2
- 240000004658 Medicago sativa Species 0.000 description 2
- 241000234295 Musa Species 0.000 description 2
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 2
- 241000208134 Nicotiana rustica Species 0.000 description 2
- 235000002637 Nicotiana tabacum Nutrition 0.000 description 2
- 244000061176 Nicotiana tabacum Species 0.000 description 2
- 240000007817 Olea europaea Species 0.000 description 2
- 235000007164 Oryza sativa Nutrition 0.000 description 2
- 235000010627 Phaseolus vulgaris Nutrition 0.000 description 2
- 241000218657 Picea Species 0.000 description 2
- 235000008124 Picea excelsa Nutrition 0.000 description 2
- 240000004713 Pisum sativum Species 0.000 description 2
- 235000010582 Pisum sativum Nutrition 0.000 description 2
- QOSMNYMQXIVWKY-UHFFFAOYSA-N Propyl levulinate Chemical compound CCCOC(=O)CCC(C)=O QOSMNYMQXIVWKY-UHFFFAOYSA-N 0.000 description 2
- 244000007021 Prunus avium Species 0.000 description 2
- 235000010401 Prunus avium Nutrition 0.000 description 2
- 240000001987 Pyrus communis Species 0.000 description 2
- 235000014443 Pyrus communis Nutrition 0.000 description 2
- 240000000528 Ricinus communis Species 0.000 description 2
- 235000004443 Ricinus communis Nutrition 0.000 description 2
- 240000000111 Saccharum officinarum Species 0.000 description 2
- 235000007201 Saccharum officinarum Nutrition 0.000 description 2
- 235000007238 Secale cereale Nutrition 0.000 description 2
- 244000082988 Secale cereale Species 0.000 description 2
- 235000002595 Solanum tuberosum Nutrition 0.000 description 2
- 244000061456 Solanum tuberosum Species 0.000 description 2
- 240000006394 Sorghum bicolor Species 0.000 description 2
- 244000046109 Sorghum vulgare var. nervosum Species 0.000 description 2
- 244000269722 Thea sinensis Species 0.000 description 2
- 244000299461 Theobroma cacao Species 0.000 description 2
- 235000009470 Theobroma cacao Nutrition 0.000 description 2
- 235000015724 Trifolium pratense Nutrition 0.000 description 2
- 244000098338 Triticum aestivum Species 0.000 description 2
- 235000007264 Triticum durum Nutrition 0.000 description 2
- 241000209143 Triticum turgidum subsp. durum Species 0.000 description 2
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 2
- 235000010749 Vicia faba Nutrition 0.000 description 2
- 240000006677 Vicia faba Species 0.000 description 2
- 240000006365 Vitis vinifera Species 0.000 description 2
- 235000014787 Vitis vinifera Nutrition 0.000 description 2
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 2
- 239000003905 agrochemical Substances 0.000 description 2
- 229910052783 alkali metal Inorganic materials 0.000 description 2
- 150000005215 alkyl ethers Chemical class 0.000 description 2
- 150000001450 anions Chemical class 0.000 description 2
- WZEMSIKSCALWJZ-UHFFFAOYSA-N azane;ethanol Chemical compound N.CCO.CCO WZEMSIKSCALWJZ-UHFFFAOYSA-N 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- 159000000007 calcium salts Chemical class 0.000 description 2
- OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Chemical compound [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 description 2
- 235000013877 carbamide Nutrition 0.000 description 2
- 150000001768 cations Chemical class 0.000 description 2
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
- 239000002270 dispersing agent Substances 0.000 description 2
- 235000013399 edible fruits Nutrition 0.000 description 2
- 239000003995 emulsifying agent Substances 0.000 description 2
- 125000004494 ethyl ester group Chemical group 0.000 description 2
- GOQYKNQRPGWPLP-UHFFFAOYSA-N heptadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCCO GOQYKNQRPGWPLP-UHFFFAOYSA-N 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 2
- 150000004702 methyl esters Chemical class 0.000 description 2
- JZMJDSHXVKJFKW-UHFFFAOYSA-M methyl sulfate(1-) Chemical compound COS([O-])(=O)=O JZMJDSHXVKJFKW-UHFFFAOYSA-M 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 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 2
- 150000002790 naphthalenes Chemical class 0.000 description 2
- GLDOVTGHNKAZLK-UHFFFAOYSA-N octadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCO GLDOVTGHNKAZLK-UHFFFAOYSA-N 0.000 description 2
- 239000004533 oil dispersion Substances 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 2
- 239000011814 protection agent Substances 0.000 description 2
- 108090000623 proteins and genes Proteins 0.000 description 2
- 235000013526 red clover Nutrition 0.000 description 2
- DCKVNWZUADLDEH-UHFFFAOYSA-N sec-butyl acetate Chemical compound CCC(C)OC(C)=O DCKVNWZUADLDEH-UHFFFAOYSA-N 0.000 description 2
- 239000002689 soil Substances 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 150000003672 ureas Chemical class 0.000 description 2
- 239000000080 wetting agent Substances 0.000 description 2
- WHOZNOZYMBRCBL-OUKQBFOZSA-N (2E)-2-Tetradecenal Chemical compound CCCCCCCCCCC\C=C\C=O WHOZNOZYMBRCBL-OUKQBFOZSA-N 0.000 description 1
- XFRVVPUIAFSTFO-UHFFFAOYSA-N 1-Tridecanol Chemical compound CCCCCCCCCCCCCO XFRVVPUIAFSTFO-UHFFFAOYSA-N 0.000 description 1
- FKKAGFLIPSSCHT-UHFFFAOYSA-N 1-dodecoxydodecane;sulfuric acid Chemical compound OS(O)(=O)=O.CCCCCCCCCCCCOCCCCCCCCCCCC FKKAGFLIPSSCHT-UHFFFAOYSA-N 0.000 description 1
- QZEDXQFZACVDJE-UHFFFAOYSA-N 2,3-dibutylnaphthalene-1-sulfonic acid Chemical class C1=CC=C2C(S(O)(=O)=O)=C(CCCC)C(CCCC)=CC2=C1 QZEDXQFZACVDJE-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
- NFAOATPOYUWEHM-UHFFFAOYSA-N 2-(6-methylheptyl)phenol Chemical compound CC(C)CCCCCC1=CC=CC=C1O NFAOATPOYUWEHM-UHFFFAOYSA-N 0.000 description 1
- DUIOKRXOKLLURE-UHFFFAOYSA-N 2-octylphenol Chemical compound CCCCCCCCC1=CC=CC=C1O DUIOKRXOKLLURE-UHFFFAOYSA-N 0.000 description 1
- CAAMSDWKXXPUJR-UHFFFAOYSA-N 3,5-dihydro-4H-imidazol-4-one Chemical compound O=C1CNC=N1 CAAMSDWKXXPUJR-UHFFFAOYSA-N 0.000 description 1
- DXPPIEDUBFUSEZ-UHFFFAOYSA-N 6-methylheptyl prop-2-enoate Chemical compound CC(C)CCCCCOC(=O)C=C DXPPIEDUBFUSEZ-UHFFFAOYSA-N 0.000 description 1
- 108010000700 Acetolactate synthase Proteins 0.000 description 1
- 235000005255 Allium cepa Nutrition 0.000 description 1
- 235000002732 Allium cepa var. cepa Nutrition 0.000 description 1
- 239000005995 Aluminium silicate Substances 0.000 description 1
- 239000004254 Ammonium phosphate Substances 0.000 description 1
- 244000144730 Amygdalus persica Species 0.000 description 1
- 235000011446 Amygdalus persica Nutrition 0.000 description 1
- 235000017060 Arachis glabrata Nutrition 0.000 description 1
- 235000018262 Arachis monticola Nutrition 0.000 description 1
- 241000894006 Bacteria Species 0.000 description 1
- ROFVEXUMMXZLPA-UHFFFAOYSA-N Bipyridyl Chemical group N1=CC=CC=C1C1=CC=CC=N1 ROFVEXUMMXZLPA-UHFFFAOYSA-N 0.000 description 1
- 244000060924 Brassica campestris Species 0.000 description 1
- 235000005637 Brassica campestris Nutrition 0.000 description 1
- 244000178924 Brassica napobrassica Species 0.000 description 1
- 235000011297 Brassica napobrassica Nutrition 0.000 description 1
- 240000000385 Brassica napus var. napus Species 0.000 description 1
- 235000001169 Brassica oleracea var oleracea Nutrition 0.000 description 1
- UCAHIIZBPCASHX-UHFFFAOYSA-N CC[N+](CC)(CC)CC1=CC=CC=C1.N Chemical compound CC[N+](CC)(CC)CC1=CC=CC=C1.N UCAHIIZBPCASHX-UHFFFAOYSA-N 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- KXDHJXZQYSOELW-UHFFFAOYSA-N Carbamic acid Chemical class NC(O)=O KXDHJXZQYSOELW-UHFFFAOYSA-N 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- 241001674939 Caulanthus Species 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- 241000370738 Chlorion Species 0.000 description 1
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 1
- 235000009088 Citrus pyriformis Nutrition 0.000 description 1
- 235000007460 Coffea arabica Nutrition 0.000 description 1
- 241000228031 Coffea liberica Species 0.000 description 1
- 244000016593 Coffea robusta Species 0.000 description 1
- 235000002187 Coffea robusta Nutrition 0.000 description 1
- 241000020428 Colea Species 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- 235000009849 Cucumis sativus Nutrition 0.000 description 1
- 235000010799 Cucumis sativus var sativus Nutrition 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
- 244000000626 Daucus carota Species 0.000 description 1
- 235000002767 Daucus carota Nutrition 0.000 description 1
- 240000003133 Elaeis guineensis Species 0.000 description 1
- 244000127993 Elaeis melanococca Species 0.000 description 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
- KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 description 1
- 235000016623 Fragaria vesca Nutrition 0.000 description 1
- 244000307700 Fragaria vesca Species 0.000 description 1
- 239000005562 Glyphosate Substances 0.000 description 1
- 240000001814 Gossypium arboreum Species 0.000 description 1
- 240000000047 Gossypium barbadense Species 0.000 description 1
- 235000004341 Gossypium herbaceum Nutrition 0.000 description 1
- 240000002024 Gossypium herbaceum Species 0.000 description 1
- 235000009432 Gossypium hirsutum Nutrition 0.000 description 1
- 244000043261 Hevea brasiliensis Species 0.000 description 1
- 235000008694 Humulus lupulus Nutrition 0.000 description 1
- 244000025221 Humulus lupulus Species 0.000 description 1
- 241000218069 Kokia 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
- 241000227653 Lycopersicon Species 0.000 description 1
- 240000003183 Manihot esculenta Species 0.000 description 1
- 235000004456 Manihot esculenta Nutrition 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical class CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 1
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 1
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 1
- IGFHQQFPSIBGKE-UHFFFAOYSA-N Nonylphenol Natural products CCCCCCCCCC1=CC=C(O)C=C1 IGFHQQFPSIBGKE-UHFFFAOYSA-N 0.000 description 1
- 235000002725 Olea europaea Nutrition 0.000 description 1
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 235000010617 Phaseolus lunatus Nutrition 0.000 description 1
- 244000100170 Phaseolus lunatus Species 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-L Phosphate ion(2-) Chemical compound OP([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-L 0.000 description 1
- 235000005205 Pinus Nutrition 0.000 description 1
- 241000218602 Pinus <genus> Species 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
- 239000004721 Polyphenylene oxide Substances 0.000 description 1
- 240000005809 Prunus persica Species 0.000 description 1
- 235000006040 Prunus persica var persica Nutrition 0.000 description 1
- 241001506137 Rapa Species 0.000 description 1
- 244000281247 Ribes rubrum Species 0.000 description 1
- 235000016911 Ribes sativum Nutrition 0.000 description 1
- 240000003768 Solanum lycopersicum Species 0.000 description 1
- 235000007230 Sorghum bicolor Nutrition 0.000 description 1
- 229940100389 Sulfonylurea Drugs 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical compound OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 description 1
- 235000006468 Thea sinensis Nutrition 0.000 description 1
- KDWQYMVPYJGPHS-UHFFFAOYSA-N Thenylchlor Chemical compound C1=CSC(CN(C(=O)CCl)C=2C(=CC=CC=2C)C)=C1OC KDWQYMVPYJGPHS-UHFFFAOYSA-N 0.000 description 1
- 235000011941 Tilia x europaea Nutrition 0.000 description 1
- 206010044278 Trace element deficiency Diseases 0.000 description 1
- 240000002913 Trifolium pratense Species 0.000 description 1
- 235000002098 Vicia faba var. major Nutrition 0.000 description 1
- 235000010716 Vigna mungo Nutrition 0.000 description 1
- 235000011453 Vigna umbellata Nutrition 0.000 description 1
- 235000009754 Vitis X bourquina Nutrition 0.000 description 1
- 235000012333 Vitis X labruscana Nutrition 0.000 description 1
- 241000607479 Yersinia pestis Species 0.000 description 1
- 235000007244 Zea mays Nutrition 0.000 description 1
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 1
- 235000016383 Zea mays subsp huehuetenangensis Nutrition 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 150000001447 alkali salts Chemical class 0.000 description 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 1
- 125000002877 alkyl aryl group Chemical group 0.000 description 1
- 125000005037 alkyl phenyl group Chemical group 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
- 150000003863 ammonium salts Chemical class 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
- 235000011130 ammonium sulphate Nutrition 0.000 description 1
- 230000008485 antagonism Effects 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 239000012752 auxiliary agent Substances 0.000 description 1
- KQCYDPMUTLJQHT-UHFFFAOYSA-N azane;methanol Chemical compound N.OC.OC KQCYDPMUTLJQHT-UHFFFAOYSA-N 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 150000001555 benzenes Chemical class 0.000 description 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
- 238000009395 breeding Methods 0.000 description 1
- 230000001488 breeding effect Effects 0.000 description 1
- 229940006460 bromide ion Drugs 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 239000001175 calcium sulphate Substances 0.000 description 1
- 235000011132 calcium sulphate Nutrition 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 239000004359 castor oil Substances 0.000 description 1
- 229960001777 castor oil Drugs 0.000 description 1
- 235000019438 castor oil Nutrition 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 239000011280 coal tar Substances 0.000 description 1
- 239000007931 coated granule Substances 0.000 description 1
- 235000005822 corn Nutrition 0.000 description 1
- 238000012272 crop production Methods 0.000 description 1
- HPXRVTGHNJAIIH-UHFFFAOYSA-N cyclohexanol Chemical compound OC1CCCCC1 HPXRVTGHNJAIIH-UHFFFAOYSA-N 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
- 239000002283 diesel fuel Substances 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-M dihydrogenphosphate Chemical compound OP(O)([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-M 0.000 description 1
- UAOMVDZJSHZZME-UHFFFAOYSA-N diisopropylamine Chemical compound CC(C)NC(C)C UAOMVDZJSHZZME-UHFFFAOYSA-N 0.000 description 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 239000010459 dolomite Substances 0.000 description 1
- 229910000514 dolomite Inorganic materials 0.000 description 1
- 238000010410 dusting Methods 0.000 description 1
- 238000012407 engineering method Methods 0.000 description 1
- 238000007046 ethoxylation reaction Methods 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- QUSNBJAOOMFDIB-UHFFFAOYSA-O ethylaminium Chemical compound CC[NH3+] QUSNBJAOOMFDIB-UHFFFAOYSA-O 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 239000003337 fertilizer Substances 0.000 description 1
- 235000004426 flaxseed Nutrition 0.000 description 1
- 235000013312 flour Nutrition 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 244000000004 fungal plant pathogen Species 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
- XDDAORKBJWWYJS-UHFFFAOYSA-N glyphosate Chemical compound OC(=O)CNCP(O)(O)=O XDDAORKBJWWYJS-UHFFFAOYSA-N 0.000 description 1
- 229940097068 glyphosate Drugs 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 235000002532 grape seed extract Nutrition 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- BXWNKGSJHAJOGX-UHFFFAOYSA-N hexadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCO BXWNKGSJHAJOGX-UHFFFAOYSA-N 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 229910017053 inorganic salt Inorganic materials 0.000 description 1
- XMBWDFGMSWQBCA-UHFFFAOYSA-M iodide Chemical compound [I-] XMBWDFGMSWQBCA-UHFFFAOYSA-M 0.000 description 1
- 229940006461 iodide ion Drugs 0.000 description 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 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
- 229920005610 lignin Polymers 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
- 239000000395 magnesium oxide Substances 0.000 description 1
- 235000012245 magnesium oxide Nutrition 0.000 description 1
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 1
- 235000019341 magnesium sulphate Nutrition 0.000 description 1
- 235000009973 maize Nutrition 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical compound CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 1
- 230000001473 noxious effect Effects 0.000 description 1
- 235000016709 nutrition Nutrition 0.000 description 1
- 230000035764 nutrition Effects 0.000 description 1
- 150000002892 organic cations Chemical group 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 235000020232 peanut Nutrition 0.000 description 1
- 229940044654 phenolsulfonic acid Drugs 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- IBBMAWULFFBRKK-UHFFFAOYSA-N picolinamide Chemical compound NC(=O)C1=CC=CC=N1 IBBMAWULFFBRKK-UHFFFAOYSA-N 0.000 description 1
- 239000001739 pinus spp. Substances 0.000 description 1
- 239000002798 polar solvent Substances 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 238000012805 post-processing Methods 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- LVTJOONKWUXEFR-FZRMHRINSA-N protoneodioscin Natural products O(C[C@@H](CC[C@]1(O)[C@H](C)[C@@H]2[C@]3(C)[C@H]([C@H]4[C@@H]([C@]5(C)C(=CC4)C[C@@H](O[C@@H]4[C@H](O[C@H]6[C@@H](O)[C@@H](O)[C@@H](O)[C@H](C)O6)[C@@H](O)[C@H](O[C@H]6[C@@H](O)[C@@H](O)[C@@H](O)[C@H](C)O6)[C@H](CO)O4)CC5)CC3)C[C@@H]2O1)C)[C@H]1[C@H](O)[C@H](O)[C@H](O)[C@@H](CO)O1 LVTJOONKWUXEFR-FZRMHRINSA-N 0.000 description 1
- FFSSWMQPCJRCRV-UHFFFAOYSA-N quinclorac Chemical compound ClC1=CN=C2C(C(=O)O)=C(Cl)C=CC2=C1 FFSSWMQPCJRCRV-UHFFFAOYSA-N 0.000 description 1
- 230000004044 response Effects 0.000 description 1
- 238000012552 review Methods 0.000 description 1
- 235000009566 rice Nutrition 0.000 description 1
- 239000012266 salt solution Substances 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 239000000741 silica gel Substances 0.000 description 1
- 229910002027 silica gel Inorganic materials 0.000 description 1
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-N sulfonic acid Chemical compound OS(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-N 0.000 description 1
- RWSOTUBLDIXVET-UHFFFAOYSA-O sulfonium Chemical compound [SH3+] RWSOTUBLDIXVET-UHFFFAOYSA-O 0.000 description 1
- 125000005537 sulfoxonium group Chemical group 0.000 description 1
- 239000001117 sulphuric acid Substances 0.000 description 1
- 235000011149 sulphuric acid Nutrition 0.000 description 1
- 238000004381 surface treatment Methods 0.000 description 1
- 229920002994 synthetic fiber Polymers 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 235000012222 talc Nutrition 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- CBXCPBUEXACCNR-UHFFFAOYSA-N tetraethylammonium Chemical compound CC[N+](CC)(CC)CC CBXCPBUEXACCNR-UHFFFAOYSA-N 0.000 description 1
- CXWXQJXEFPUFDZ-UHFFFAOYSA-N tetralin Chemical compound C1=CC=C2CCCCC2=C1 CXWXQJXEFPUFDZ-UHFFFAOYSA-N 0.000 description 1
- QEMXHQIAXOOASZ-UHFFFAOYSA-N tetramethylammonium Chemical compound C[N+](C)(C)C QEMXHQIAXOOASZ-UHFFFAOYSA-N 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 235000018322 upland cotton Nutrition 0.000 description 1
- 235000020234 walnut Nutrition 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
- 239000004562 water dispersible granule Substances 0.000 description 1
- 239000004563 wettable powder Substances 0.000 description 1
- 239000002023 wood 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
- A01N43/34—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
- A01N43/40—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom six-membered rings
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)
Abstract
本发明涉及一种包含如下组分的除草混合物:A)picolinafen(I),或其可农用盐,和B)至少一种选自邻氨甲酰苯甲酸酯类(B1)、缩氨基脲类(B2)、乙酰氯苯胺类(B3)、氨基甲酸酯类(B4)、哒嗪类(B5)、二硝基酚类(B6)、联吡啶类(B7)、苯并噻二唑类(B8)、尿嘧啶类(B9)、哒嗪酮类(B10)、苯基氨基甲酸酯类(B11)、苯甲酸类(B12)、喹啉羧酸类(B13)、腈类(B14)、苯甲酰胺类(B15)和酰胺类(B16)的其他除草剂。
Description
本发明涉及一种除草混合物,包含如下组分:
A)picolinafen(I):
或其可农用盐;
和
B)至少一种选自如下的其他除草剂:邻氨甲酰苯甲酸酯类(B1)、缩氢基脲类(B2)、乙酰氯苯胺类(B3)、氨基甲酸酯类(B4)、哒嗪类(B5)、二硝基酚类(B6)、联吡啶(dipyridylene)类(B7)、苯并噻二唑类(B8)、尿嘧啶类(B9)、哒嗪酮类(B10)、苯基氨基甲酸酯类(B11)、苯甲酸类(B12)、喹啉羧酸类(B13)、腈类(B14)、苯甲酰胺类(B15)和酰胺类(B16);
和若需要的话,
C)选自isoxadifen、吡咯二酸和喹氧乙酸的安全剂。
此外,本发明还涉及包含组分A、B和需要的话组分C的混合物以及至少一种液体和/或固体载体和需要的话,至少一种表面活性剂的除草组合物。
此外,本发明涉及制备这些混合物或组合物的方法以及防治不希望的植物生长的方法。
吡啶酰胺与其他特异性除草剂的混合物由WO 94/07368和WO01/26466已知。对于作物保护组合物,原则上希望增加活性化合物的特异性活性并提高作用的安全性。本发明的目的是增加picolinafen的活性。
我们发现该目的由开头所定义的混合物实现。此外,我们发现了包含这些混合物的除草组合物以及它们的制备方法和防治不希望的植物生长的方法。在最后提到的方法中,组分A、B和需要的话,C是否联合或单独配制和施用且在单独施用的情况下以何种顺序施用并不重要。
本发明的混合物显示出协同增效作用;除草活性组分A)和B)与某些作物植株的相容性通常得以维持。然而,可能希望以观察到安全效果的量使用组分C)。
按照本发明可以与picolinafen(A)和若需要的话组分C)组合使用的除草剂的实例尤其是:
B1:邻氨甲酰苯甲酸酯类,例如:
抑草生;
B2:缩氨基脲类,例如:
二氟吡隆;
B3:乙酰氯苯胺类,例如:
噻吩草胺、S-噻吩草胺、乙草胺、甲草胺、丁草胺、丁烯草胺、安塔、克草胺、吡草胺、异丙甲草胺、S-异丙甲草胺、丙草胺、扑草胺、广草胺、猛杀草、噻醚草胺或二甲苯草胺;
B4:氢基甲酸酯类,例如:
黄草灵、长杀草、氯苯胺灵、坪草丹、拿草特、苯胺灵或丁草威;
B5:哒嗪类,例如:
氟硫草定或噻氟啶草;
B6:二硝基酚类,例如:
杀草全、地乐酚、地乐酯、地乐消酚或二硝甲酚;
B7:联吡啶类,例如:
莎草快、苯敌快、敌草快阳离子或对草快;
B8:苯并噻二唑类,例如:
噻草平;
B9:尿嘧啶类,例如:
除草定、异草定、环草定或特草定;
B10:哒嗪酮类,例如:
杀草敏;
B11:苯基氨基甲酸酯类,例如:
异苯敌草或苯敌草;
B12:苯甲酸类,例如:
草灭平或麦草畏;
B13:喹啉羧酸类,例如:
二氯喹啉酸(quinchlorac)或喹草酸;
B14:腈类,例如:
dichlorbenil或草克乐;
B15:苯甲酰胺类,例如:
异恶草胺;
B16:酰胺类,例如:
草毒死、新燕灵、溴丁酰草胺、草乃敌、乙苯酰草(benzochlomet)、膦铵素或杀草利;
及其可农用盐,或若该化合物为羧酸,则可为其可农用酯、硫代酸酯或酰胺类。
Picolinafen由EP 447 004已知。
组分B)的除草剂由以下文献已知:
-“Herbizide”[除草剂],B.Hock,C.Fedtke,R.R.Schmidt,第1版,Thieme 1995(二氯喹啉酸(第238页),丁草胺(第32页),丙草胺(第32页),氟硫草定(第32页),溴丁酰草胺(第243页),噻草平(第30页),氯苯胺灵(第205页);
-“Agricultural Chemicals”,Book II Herbicides,1993(乙苯酰草(HW-52)(第54页),噻吩草胺(第48页),喹草酸(第233页),吡草胺(第64页),杀草全(第228页),噻氟啶草(第226页));
-“Agricultural Chemicals”,Book II Herbicides,第13版(二氟吡隆(第90页),丁烯草胺(第54页),丁草威(第84页));
-Farm Chemicals Handbook 1994,Meister Publishing Company 1994(异草定(第C.200页));
-“Short Review of Herbicides & PGRs”1991,Hodogaya Chemicals(噻醚草胺(NSK-850)(第52页),草毒死(第48页),新燕灵(第38页),草克乐(第150页),草乃敌(第34页),膦铵素(第232页),异恶草胺(第42页),杀草利(第32页),抑草生(第36页),拿草特(第34页),草灭平(第28页),麦草畏(第26页),黄草灵(第112页),长杀草(第36页),异苯敌草(第104页),坪草丹(第112页),苯敌草(第104页),苯胺灵(第100页),乙草胺(第48页),甲草胺(第46页),安塔(第48页),demethachlor(第50页),异丙甲草胺(第46页),扑草胺(第44页),广草胺(第44页),猛杀草(第48页),二甲苯草胺(第52页),地乐酚(第128页),地乐酯(第128页),地乐消酚(第128页),二硝甲酚(第126页),莎草快(第158页),苯敌快(第160页),敌草快阳离子(第158页),对草快(第158页),杀草敏(第174页),除草定(第180页),环草定(第180页),特草定(第180页),dichlorbenil(第148页),猛杀草(第48页))。
组分C)的安全剂由以下文献已知:
-B.Hock,C.Fedtke,R.R.Schmidt,第1版,Thieme 1995(喹氧乙酸(第266页));
-Agrow 293(11.28.97)(吡咯二酸);
-Agrow 324(03.12.99)(isoxadifen)。
本发明的活性化合物可以纯对映体以及外消旋体或非对映体混合物形式存在和使用。
此外,活性化合物可以其可农用盐形式使用且若化合物为羧酸,则也可以其可农用酯、硫代酸酯和酰胺形式使用。
合适的盐通常为其阳离子或阴离子或酯、硫代酸酯和酰胺对除草作用或安全作用没有不利影响的那些阳离子的盐、那些酸的酸加成盐或酯、硫代酸酯和酰胺。
合适的阳离子尤其是碱金属阳离子如锂、钠或钾,或碱土金属阳离子如镁或钙。还合适的是有机阳离子,如鏻离子,锍离子,优选三(C1-C4烷基)锍,如三甲基锍,氧化锍离子,优选三(C1-C4烷基)氧化锍。同样合适的是铵,其中需要的话1-4个氢原子可以被C1-C4烷基、羟基-C1-C4烷基、C1-C4烷氧基-C1-C4烷基、羟基-C1-C4烷氧基-C1-C4烷基、苯基或苄基代替,优选铵、甲基铵、二甲基铵、三甲基铵、四甲基铵、四乙基铵、异丙基铵、二异丙基铵、四丁基铵、乙醇铵、二乙醇铵、2-(2-羟基乙氧基)乙基铵、苄基三甲基铵或苄基三乙基铵。
有用的酸加成盐的阴离子主要是卤离子如氟离子、氯离子、溴离子、碘离子、硝酸根、硫酸氢根、硫酸根、磷酸二氢根、磷酸氢根、磷酸根、甲基硫酸根、碳酸氢根和碳酸根。
合适的酯例如是直链或支化的C1-C10烷基酯,尤其是甲基、乙基、丙基、异丙基、丁基、异丁基或异辛基酯,或直链或支化的C1-C4烷氧基-C1-C4烷基酯,尤其是甲氧基乙基、乙氧基乙基或丁氧基乙基酯。硫代酸酯的实例是直链或支化的C1-C10烷基硫代酸酯,尤其是乙基硫代酸酯。适合用作酰胺类的尤其是甲基酰胺类或二甲基酰胺类,以及N-酰苯胺,如N-酰苯胺本身或2-氯-N-酰苯胺。
在优选的实施方案中,本发明的除草混合物包含如下组分:
A)picolinafen或其可农用盐;和
B)至少一种选自如下的其他除草剂:
B1:邻氨甲酰苯甲酸酯类,例如:
抑草生;
B2:缩氨基脲类,例如:
二氟吡隆;
B3:乙酰氯苯胺类,例如:
噻吩草胺、S-噻吩草胺、乙草胺、甲草胺、丁草胺、丁烯草胺、安塔、克草胺、吡草胺、异丙甲草胺、S-异丙甲草胺、丙草胺、扑草胺、广草胺、猛杀草、噻醚草胺或二甲苯草胺;
B4:氨基甲酸酯类,例如:
黄草灵、长杀草、氯苯胺灵、坪草丹、拿草特、苯胺灵或丁草威;
B5:哒嗪类,例如:
氟硫草定或噻氟啶草;
B6:二硝基酚类,例如:
杀草全、地乐酚、地乐酯、地乐消酚或二硝甲酚;
B7:联吡啶类,例如:
莎草快、苯敌快、敌草快阳离子或对草快;
B8:苯并噻二唑类,例如:
噻草平;
B9:尿嘧啶类,例如:
除草定、异草定、环草定或特草定;
B10:哒嗪酮类,例如:
杀草敏;
B11:苯基氨基甲酸酯类,例如:
异苯敌草或苯敌草;
B12:苯甲酸类,例如:
草灭平或麦草畏;
B13:喹啉羧酸类,例如:
二氯喹啉酸或喹草酸;
B14:腈类,例如:
dichlorbenil或草克乐;
B15:苯甲酰胺类,例如:
异恶草胺;
B16:酰胺类,例如:
草毒死、新燕灵、溴丁酰草胺、草乃敌、乙苯酰草(benzochlomet)、膦铵素或杀草利;
及其可农用盐,或若该化合物为羧酸,则为其可农用酯、硫代酸酯或酰胺。
在特别优选的实施方案中,本发明的除草混合物包含如下组分:
A)picolinafen或其可农用盐;和
B)至少一种选自如下的其他除草剂:
B7:联吡啶类,例如
莎草快、苯敌快、敌草快阳离子或对草快;
B8:苯并噻二唑类,例如
噻草平;
B9:尿嘧啶类,例如
除草定、异草定、环草定或特草定;
B12:苯甲酸类,例如
草灭平或麦草畏;
B13:喹啉羧酸类,例如
二氯喹啉酸或喹草酸,尤其是二氯喹啉酸;
B15:苯甲酰胺类,例如
异恶草胺;
及其可农用盐,或若该化合物为羧酸,则为其可农用酯、硫代酸酯或酰胺。
在尤其优选的实施方案中,本发明的除草混合物包含如下组分:
A)picolinafen或其可农用盐;和
B)至少一种选自如下的其他除草剂:
B7:联吡啶类,例如
莎草快、苯敌快、敌草快阳离子或对草快;
B8:苯并噻二唑类,例如
噻草平;
B12:苯甲酸类,例如
草灭平或麦草畏;
B15:苯甲酰胺类,例如
异恶草胺;
及其可农用盐,或若该化合物为羧酸,则为其可农用酯、硫代酸酯或酰胺。
额外优选的是包含picolinafen+苯敌快、picolinafen+对草快、picolinafen+噻草平、picolinafen+异草定、picolinafen+麦草畏、picolinafen+二氯喹啉酸、picolinafen+喹草酸或picolinafen+异恶草胺的除草混合物。
在最为优选的实施方案中,该除草混合物包含picolinafen+苯敌快、picolinafen+噻草平、picolinafen+麦草畏或picolinafen+异恶草胺。
若该混合物包含活性化合物对草快或苯敌快,则还优选其中上述活性化合物以氯化物、溴化物或甲基硫酸盐存在的那些混合物。
若该混合物包含活性化合物噻草平、麦草畏或二氯喹啉酸,则还优选其中上述活性化合物以三甲基锍、铵、钠、钾、镁或钙盐存在的那些混合物。
若该混合物包含活性化合物麦草畏或二氯喹啉酸,则还优选其中上述活性化合物被其乙醇铵、二乙醇铵、甲基铵、二甲基铵、三甲基铵、异丙基铵或2-(2-羟基乙氧基)乙基铵盐、其甲基酰胺或二甲基酰胺、其N-酰苯胺或2-氯-N-酰苯胺、其甲酯、乙酯、丙酯、异丙酯、丁酯、异丁酯、异辛酯、甲氧基乙酯、乙氧基乙酯、丁氧基乙酯或其乙基硫代酸酯代替的那些混合物。
在进一步优选的实施方案中,本发明的除草混合物包含如下组分:
A)picolinafen或其可农用盐;和
B)至少一种选自如下的其他除草剂:
B8:苯并噻二唑类,例如
噻草平;
B12:苯甲酸类,例如
草灭平或麦草畏;
B13:喹啉羧酸类,例如
二氯喹啉酸或喹草酸;
B15:苯甲酰胺类,例如
异恶草胺;
及其可农用盐,或若该化合物为羧酸,则为其可农用酯、硫代酸酯或酰胺。
额外优选包含picolinafen+二氯喹啉酸、picolinafen+喹草酸或pincolinofen+异恶草胺的除草混合物。
若该混合物包含活性化合物噻草平、麦草畏、二氯喹啉酸或喹草酸,则还优选其中上述活性化合物以三甲基锍、铵、钠、钾、镁或钙盐存在的那些混合物。
若该混合物包含活性化合物麦草畏、二氯喹啉酸或喹草酸,则还优选其中上述活性化合物被其乙醇铵、二甲醇铵、甲基铵、二甲基铵、三甲基铵、异丙基铵或2-(2-羟基乙氧基)乙基铵盐、不包括其甲基酰胺或二甲基酰胺、其N-酰苯胺或2-氯-N-酰苯胺、以及其甲酯、乙酯、丙酯、异丙酯、丁酯、异丁酯、异辛酯、甲氧基乙酯、乙氧基乙酯、丁氧基乙酯或其乙基硫代酸酯代替的那些混合物。
在另一特别优选的实施方案中,本发明的除草混合物包含如下组分:
A)picolinafen或其可农用盐;和
B)至少一种选自如下的其他除草剂:
B2:缩氨基脲类,例如:
二氟吡隆;
B3:乙酰氯苯胺类,例如:
乙草胺、安塔、克草胺、广草胺、猛杀草、噻醚草胺或二甲苯草胺;
B4:氨基甲酸酯类,例如:
长杀草、氯苯胺灵、拿草特或苯胺灵;
B6:二硝基酚类,例如:
杀草全、地乐酚、地乐酯或二硝甲酚;
B7:联吡啶类,例如:
莎草快、苯敌快、敌草快阳离子或对草快;
B9:尿嘧啶类,例如:
异草定或环草定;
B10:哒嗪酮类,例如:
杀草敏;
B11:苯基氨基甲酸酯类,例如:
异苯敌草或苯敌草;
B13:喹啉羧酸类,例如:
二氯喹啉酸或喹草酸;
B15:苯甲酰胺类,例如:
异恶草胺;
B16:酰胺类,例如:
草毒死、新燕灵、草乃敌、乙苯酰草(benzochlomet)、膦铵素或杀草利;及其可农用盐,或若该化合物为羧酸,则为其可农用酯、硫代酸酯或酰胺。
在特别优选的实施方案中,本发明的除草混合物包含picolinafen+苯敌快或picolinafen+异恶草胺。
在另一特别优选的实施方案中,本发明的除草混合物包含如下组分:
A)picolinafen或其可农用盐;和
B)至少一种选自如下的其他除草剂:
B1:邻氨甲酰苯甲酸酯类,例如:
抑草生;
B2:缩氨基脲类,例如:
二氟吡隆;
B3:乙酰氯苯胺类,例如:
噻吩草胺、S-噻吩草胺、乙草胺、甲草胺、丁草胺、丁烯草胺、安塔、克草胺、吡草胺、异丙甲草胺、S-异丙甲草胺、丙草胺、扑草胺、广草胺、猛杀草、噻醚草胺或二甲苯草胺;
B4:氨基甲酸酯类,例如:
黄草灵、长杀草、氯苯胺灵、坪草丹、拿草特、苯胺灵或丁草威;
B5:哒嗪类,例如:
氟硫草定或噻氟啶草;
B6:二硝基酚类,例如:
杀草全、地乐酚、地乐酯、地乐消酚或二硝甲酚;
B7:联吡啶类,例如:
莎草快、苯敌快、敌草快阳离子或对草快;
B8:苯并噻二唑类,例如:
噻草平;
B9:尿嘧啶类,例如:
除草定、异草定、环草定或特草定;
B10:哒嗪酮类,例如:
杀草敏;
B11:苯基氨基甲酸酯类,例如:
异苯敌草或苯敌草;
B12:苯甲酸类,例如:
草灭平或麦草畏;
B13:喹啉羧酸类,例如:
二氯喹啉酸或喹草酸;
B14:腈类,例如:
dichlorbenil或草克乐;
B15:苯甲酰胺类,例如:
异恶草胺;
B16:酰胺类,例如:
草毒死、新燕灵、溴丁酰草胺、草乃敌、乙苯酰草(benzochlomet)、膦铵素或杀草利;
及其可农用盐,或若该化合物为羧酸,则为其可农用酯、硫代酸酯或酰胺;和
C)选自isoxadifen,优选isoxadifen“酸”或isoxadifen-ethyl,尤其是isoxadifen-ethyl;吡咯二酸,优选游离吡咯二酸或吡咯二酸二乙酯,尤其是吡咯二酸二乙酯;和喹氧乙酸,优选游离喹氧乙酸、喹氧乙酸异庚酯或喹氧乙酸异庚酯×n水合物(n=2-6),尤其是喹氧乙酸异庚酯的安全剂。
在另一特别优选的实施方案中,本发明的除草混合物包含如下组分:
A)picolinafen或其可农用盐,和
B)至少一种选自如下的其他除草剂:
B1:邻氨甲酰苯甲酸酯类,例如
抑草生;
B2:缩氨基脲类,例如
二氟吡隆;
B3:乙酰氯苯胺类,例如
噻吩草胺、S-噻吩草胺、乙草胺、甲草胺、丁草胺、丁烯草胺、安塔、克草胺、吡草胺、异丙甲草胺、S-异丙甲草胺、丙草胺、扑草胺、广草胺、猛杀草、噻醚草胺或二甲苯草胺;
B4:氨基甲酸酯类,例如
黄草灵、长杀草、氯苯胺灵、坪草丹、拿草特、苯胺灵或丁草威;
B5:哒嗪类,例如
氟硫草定或噻氟啶草;
B6:二硝基酚类,例如
杀草全、地乐酚、地乐酯、地乐消酚,或二硝甲酚;
B10:哒嗪酮类,例如
杀草敏;
B11:苯基氨基甲酸酯类,例如
异苯敌草或苯敌草;
B14:腈类,例如
dichlorbenil或草克乐;
B15:苯甲酰胺类,例如
异恶草胺;
B16:酰胺类,例如
草毒死、新燕灵、溴丁酰草胺、草乃敌、乙苯酰草(benzochlomet)、膦铵素或杀草利;
及其可农用盐;和
C)选自isoxadifen,优选isoxadifen“酸”或isoxadifen-ethyl,尤其是isoxadifen-ethyl;吡咯二酸,优选游离吡咯二酸或吡咯二酸二乙酯,尤其是吡咯二酸二乙酯;和喹氧乙酸,优选游离喹氧乙酸、喹氧乙酸异庚酯或喹氧乙酸异庚酯×n水合物(n=2-6),尤其是喹氧乙酸异庚酯的安全剂。
在另一优选的实施方案中,该除草混合物包含如下组分:
A)picolinafen或其可农用盐;和
B)至少一种选自如下的其他除草剂:
B7:联吡啶类,例如
莎草快、苯敌快、敌草快阳离子或对草快;
B8:苯并噻二唑类,例如
噻草平;
B9:尿嘧啶类,例如
除草定、环草定、特草定或异草定;
B12:苯甲酸类,例如
草灭平或麦草畏;
B13:喹啉羧酸类,例如
二氯喹啉酸或喹草酸;
及其可农用盐,或若该化合物为羧酸,则为其可农用酯、硫代酸酯或酰胺;和
C)选自isoxadifen,优选isoxadifen“酸”或isoxadifen-ethyl,尤其是isoxadifen-ethyl;吡咯二酸,优选游离吡咯二酸或吡咯二酸二乙酯,尤其是吡咯二酸二乙酯;和喹氧乙酸,优选游离喹氧乙酸,喹氧乙酸异庚酯或喹氧乙酸异庚酯×n水合物(n=2-6),尤其是喹氧乙酸异庚酯的安全剂。
在特别优选的实施方案中,该除草混合物包含如下组分:
A)picolinafen或其可农用盐;和
B)至少一种选自如下的其他除草剂:苯敌快、对草快、噻草平、异草定、麦草畏和二氯喹啉酸;或其可农用盐,或若该除草剂为羧酸,则为其可农用酯、硫代酸酯或酰胺;和
C)isoxadifen-ethyl。
在另一特别优选的实施方案中,该除草混合物包含如下组分:
A)picolinafen或其可农用盐;和
B)至少一种选自如下的其他除草剂:苯敌快、对草快、噻草平、异草定、麦草畏和二氯喹啉酸;或其可农用盐,或若该除草剂为羧酸,则为其可农用酯、硫代酸酯或酰胺;和
C)吡咯二酸二乙酯。
在另一特别优选的实施方案中,该除草混合物包含如下组分:
A)picolinafen或其可农用盐;和
B)至少一种选自如下的其他除草剂:苯敌快、对草快、噻草平、异草定、麦草畏和二氯喹啉酸;或其可农用盐,或若该除草剂为羧酸,则为其可农用酯、硫代酸酯或酰胺;和
C)喹氧乙酸,优选游离喹氧乙酸、喹氧乙酸异庚酯或喹氧乙酸异庚酯×n水合物(n=2-6),尤其是喹氧乙酸异庚酯。
在另一优选实施方案中,该除草混合物除了picolinafen外仅包含一种选自B)组的其他除草剂。
对应的优选情况类似于上面所说的。
在进一步优选的实施方案中,该除草混合物除了picolinafen外仅包含一种选自B)组的其他除草剂且仅包含一种选自C)组的安全剂。
对应的优选情况类似于上面所说的。
组分A和B以协同增效有效量施用;组分A)与B)的混合比通常为1∶0.1-1∶50,优选1∶0.2-1∶20。
若还使用安全剂C),则组分A)∶B)∶C)的混合比在1∶0.1∶0.1-1∶50∶10,优选1∶0.2∶0.2-1∶20∶4的重量比内。
本发明还涉及包含除草有效量的除草混合物(包含上述组分A)、B)和需要的话C))、至少一种液体和/或固体载体和需要的话,至少一种表面活性剂的除草组合物。
本发明的除草混合物和除草组合物可以在诸如玉米、禾谷类、稻和大豆,尤其是禾谷类的作物中非常良好地防治阔叶杂草和禾本科杂草,而不损害作物植株,尤其在低施用率下也发生该作用。
考虑到施用方法的多样性,本发明的协同增效除草混合物和除草组合物可以额外用于许多其他作物中以消除不希望的植物。合适的作物实例如下:洋葱(Allium cepa)、凤梨(Ananas comosus)、落花生(Arachis hypogaea)、石刁柏(Asparagus officinalis)、甜菜(Beta vulgaris spp.altissima)、甜菜(Beta vulgaris spp.rapa)、欧洲油菜(Brassica napus var.napus)、芜青甘蓝(Brassica napus var.napobrassica)、芜青(Brassica rapa var.silvestris)、大叶茶(Camellia sinensis)、红花(Carthamus tinctorius)、美国山核桃(Caryaillinoinensis)、柠檬(Citrus limon)、甜橙(Citrus sinensis)、小果咖啡(Coffeaarabica)(中果咖啡(Coffea canephora)、大果咖啡(Coffea liberica))、黄瓜(Cucumis sativus)、狗牙根(Cynodon dactylon)、Daucus carota、油棕(Elaeisguineensis)、欧洲草莓(Fragaria vesca)、大豆(Glycine max)、陆地棉(Gossypium hirsutum)(树棉(Gossypium arboreum)、草棉(Gossypiumherbaceum)、Gossypium vitifolium)、向日葵(Helianthus annuus)、Heveabrasiliensis、大麦(Hordeum vulgare)、啤酒花(Humulus lupulus)、甘薯(Ipomoea batatas)、核桃(Juglans regia)、兵豆(Lens culinaris)、亚麻(Linumusitatissimum)、番茄(Lycopersicon lycopersicum)、苹果属(Malus spp.)、Manihot esculenta、紫苜蓿(Medicago sativa)、芭蕉属(Musa spp.)、烟草(Nicotiana tabacum)(黄花烟草(N.rustica))、油橄榄(Olea europaea)、稻(Oryza sativa)、金甲豆(Phaseolus lunatus)、菜豆(Phaseolus vulgaris)、黑挪威云杉(Picea abies)、松属(Pinus spp.)、豌豆(Pisum sativum)、欧洲甜樱桃(Prunus avium)、桃(Prunus persica)、西洋梨(Pyrus communis)、Ribessylvestre、蓖麻(Ricinus communis)、甘蔗(Saccharum officinarum)、黑麦(Secale cereale)、马铃薯(Solanum tuberosum)、两色蜀黍(Sorghumbicolor)(蜀黍(s.vulgare))、可可树(Theobroma cacao)、红车轴草(Trifoliumpratense)、普通小麦(Triticum aestivum)、硬粒小麦(Triticum durum)、蚕豆(Vicia faba)、葡萄(Vitis vinifera)和玉蜀黍(Zea mays)。
此外,本发明的除草混合物和除草组合物还可以用于因包括基因工程方法在内的育种而耐受除草剂作用的作物中。合适的是优选耐受草甘膦或除草的乙酰乳酸合成酶抑制剂如磺酰脲或咪唑啉酮的基因工程改性禾谷类作物。
本发明的混合物或包含它们的除草组合物例如可以通过喷雾、雾化、撒粉、撒播或浇灌以直接可喷水溶液、粉末、悬浮液、高度浓缩的水性、油性或其它悬浮液或分散体、乳液、油分散体、糊、粉剂、撒播用材料或颗粒形式施用。
施用形式取决于意欲的目的;在各种情况下都应确保本发明的活性化合物尽可能最精细地分布。
除草组合物包含组分A)、B)和需要的话,C)以及常用于配制作物保护剂的助剂。
合适的惰性添加剂是中沸点到高沸点的矿物油馏分如煤油和柴油,此外还有煤焦油和植物或动物来源的油,脂族、环状和芳族烃如石蜡、四氢化萘、烷基化萘或其衍生物、烷基化苯或其衍生物,醇类如甲醇、乙醇、丙醇、丁醇和环己醇,酮类如环己酮,强极性溶剂如N-甲基吡咯烷酮或水。
含水使用形式可通过添加水由乳油、悬浮液、糊、可湿性粉末或水分散性颗粒制备。为了制备乳液、糊或油分散体,可使用湿润剂、增粘剂、分散剂或乳化剂将组分A)、B)和需要的话,C)直接或溶于油或溶剂之后在水中均化。或者,也可制备包含活性化合物、湿润剂、增粘剂、分散剂或乳化剂和若合适的话溶剂或油的浓缩物,并且这些浓缩物适于用水稀释。
合适的表面活性剂是芳族磺酸如木素磺酸、苯酚磺酸、萘磺酸和二丁基萘磺酸以及脂肪酸、烷基磺酸、烷基芳基磺酸、烷基硫酸、月桂基醚硫酸和脂肪醇硫酸的碱金属盐、碱土金属盐和铵盐,硫酸化十六烷醇、十七烷醇和十八烷醇以及脂肪醇乙二醇醚的盐,磺化萘及其衍生物与甲醛的缩合物,萘或萘磺酸与苯酚和甲醛的缩合物,聚氧乙烯辛基苯基醚,乙氧基化的异辛基酚、辛基酚或壬基酚,烷基苯基聚乙二醇醚,三丁基苯基聚乙二醇醚,烷基芳基聚醚醇,异十三烷醇,脂肪醇/氧化乙烯缩合物,乙氧基化蓖麻油,聚氧乙烯烷基醚或聚氧丙烯烷基醚,月桂醇聚乙二醇醚乙酸酯,山梨醇酯,木素亚硫酸盐废液或甲基纤维素。
粉末、撒播用材料和粉剂可通过将协同增效除草混合物或单独的活性化合物与固体载体混合或同时研磨而制备。
可通过将活性成分与固体载体粘附而制备颗粒,如包膜颗粒、浸渍颗粒和均相颗粒。固体载体为矿土,例如硅酸、硅胶、硅酸盐、滑石、高岭土、石灰石、石灰、白垩、红玄武土、黄土、粘土、白云石、硅藻土、硫酸钙、硫酸镁、氧化镁、磨碎的合成材料,肥料如硫酸铵、磷酸铵、硝酸铵、尿素,植物来源的产物如谷粉、树皮粉、木粉和坚果壳粉,纤维素粉或其它固体载体。
本发明混合物在即用产品中的浓度可在宽范围内变化。通常而言,配制剂包含约0.001-98重量%,优选0.01-95重量%,尤其是0.5-90重量%活性化合物。
组分A)、B)和需要的话,C)的活性化合物可以联合配制,但也可单独配制,和/或联合或单独施用于植物、其栖息地和/或种子上。优选同时施用活性化合物。然而也可以单独施用它们。
此外,可能有用的是将本发明的除草混合物或除草组合物与其他作物保护剂联合或单独施用,例如与用于防治害虫或植物病原性真菌或细菌的试剂联合或单独施用。此外还有利的是与用于治疗营养和痕量元素缺乏症的无机盐溶液溶混。也可以加入非植物毒性油和油浓缩物。
本发明混合物和除草组合物可以通过出苗前方法或出苗后方法施用。若活性化合物不能被某些作物良好耐受,则可使用其中借助喷雾设备喷雾除草组合物的施用技术,以使它们尽可能不接触敏感性作物的叶子,同时活性化合物达到生长在下面的不希望的植物的叶子或达到裸露的土壤表面(后定向,最后耕作程序)。
在出苗后处理的情况下,本发明的除草组合物主要通过喷雾于叶子而施用于植物上。这里,施用可以通过例如以水作为载体的常规喷雾技术进行,其中喷雾液的量为约100-1000L/ha。组合物还可以通过低容量和超低容量方法施用或以颗粒形式施用。
纯活性化合物混合物(即A)、B)和需要的话,C),没有配制助剂)的所需施用率取决于植物丛的组成以及植物的发育阶段、气候条件和施用技术,通常为0.001-3kg/ha,优选0.01-2.5kg/ha,尤其是0.01-1.0kg/ha活性物质(a.s.)。
picolinafen的施用率通常为0.01-0.5kg/ha活性物质(a.s.)。
组分B)的施用率通常为0.01-2.0kg/ha活性物质(a.s.)。
组分C)的施用率通常为0.01-0.5kg/ha活性物质(a.s.)。
应用实施例
本发明的混合物通过出苗前方法或出苗后方法施用(叶面处理)。
一些试验是温室试验,而另一些试验在小块田(在具有砂壤土(pH6.2-7.0)或砂土(pH 5.0-6.7)的地方)中敞开进行。
有害植物具有不同尺寸且呈不同发育阶段,平均5-20cm,这取决于它们的习性。
组分A)和B)以及需要的话,安全剂C)的除草活性化合物依次或联合以乳液、水溶液或悬浮液形式施用,其中所用载体为水(300-400L/ha),在联合施用的情况下有时以桶混物且有时以现混物施用。在敞开试验情况下,借助可移动喷雾器进行施用。
试验周期长达3-8周;还在随后的时间点观察植物丛。
除草组合物引起的损害与未处理对照相比以0-100%的范围进行评价。0表示没有损害且100表示植物完全损害。
下列实施例说明可以按照本发明使用的除草组合物的效果,但不排除其他应用的可能性。
在这些实施例中,使用S.R.Colby(计算除草组合的协同增效和拮抗响应,Weeds 15,第20页及随后各页(1967))的方法计算若各活性成分化合物仅产生加合作用时可预期的值E。
基于下式进行计算:
E=X+Y-(X·Y/100)
其中
X=以施用率a施用的组分A)的除草作用,以%表示;
Y=以施用率b施用的组分B)的除草作用,以%表示;
E=以施用率a+b施用的组分A)+B)的除草作用,以%表示。
如果观察到的值超过使用Colby公式计算的值E,则存在协同效果。
在合适施用率下通过出苗后方法施用的本发明除草混合物,例如picolinafen+苯敌快、picolinafen+噻草平、picolinafen+麦草畏或picolinafen+异恶草胺,具有比基于单独使用时各组分的观察效果根据Colby预期的除草作用更有效的除草作用。
Claims (11)
1.除草混合物,包含如下组分:
A)picolinafen(I):
或其可农用盐,
和
B)至少一种选自如下的其他除草剂:邻氨甲酰苯甲酸酯类(B1)、缩氨基脲类(B2)、乙酰氯苯胺类(B3)、氨基甲酸酯类(B4)、哒嗪类(B5)、二硝基酚类(B6)、联吡啶类(B7)、苯并噻二唑类(B8)、尿嘧啶类(B9)、哒嗪酮类(B10)、苯基氨基甲酸酯类(B11)、苯甲酸类(B12)、喹啉羧酸类(B13)、腈类(B14)、苯甲酰胺类(B15)和酰胺类(B16)。
2.如权利要求1所要求的除草混合物,包含至少一种选自B1-B16组的除草化合物作为组分B):
B1:邻氨甲酰苯甲酸酯类:
抑草生;
B2:缩氨基脲类:
二氟吡隆;
B3:乙酰氯苯胺类:
噻吩草胺、S-噻吩草胺、乙草胺、甲草胺、丁草胺、丁烯草胺、安塔、克草胺、吡草胺、异丙甲草胺、S-异丙甲草胺、丙草胺、扑草胺、广草胺、猛杀草、噻醚草胺或二甲苯草胺;
B4:氨基甲酸酯类:
黄草灵、长杀草、氯苯胺灵、坪草丹、拿草特、苯胺灵或丁草威;
B5:哒嗪类:
氟硫草定或噻氟啶草;
B6:二硝基酚类:
杀草全、地乐酚、地乐酯、地乐消酚或二硝甲酚;
B7:联吡啶类:
莎草快、苯敌快、敌草快阳离子或对草快;
B8:苯并噻二唑类:
噻草平;
B9:尿嘧啶类:
除草定、异草定、环草定或特草定;
B10:哒嗪酮类:
杀草敏;
B11:苯基氨基甲酸酯类:
异苯敌草或苯敌草;
B12:苯甲酸类:
草灭平或麦草畏;
B13:喹啉羧酸类:
二氯喹啉酸或喹草酸;
B14:腈类:
dichlorbenil或草克乐;
B15:苯甲酰胺类:
异恶草胺;
B16:酰胺类:
草毒死、新燕灵、溴丁酰草胺、草乃敌、乙苯酰草(benzochlomet)、膦铵素或杀草利;
及其可农用盐,或若该化合物为羧酸,则为其可农用酯、硫代酸酯或酰胺。
3.如权利要求1或2所要求的除草混合物,包含作为组分B)的至少一种选自B7、B8、B9、B12、B13和B15组的除草剂。
4.如权利要求1-3中任一项所要求的除草混合物,包含作为组分B)的选自苯敌快、对草快、噻草平、异草定、麦草畏、二氯喹啉酸、喹草酸和异恶草胺的除草剂。
5.如权利要求1-4中任一项所要求的除草混合物,包含作为组分C)的选自isoxadifen、吡咯二酸和喹氧乙酸的安全剂。
6.如权利要求1-4中任一项所要求的除草混合物,其中组分A)和组分B)以1∶0.1-1∶50的重量比存在。
7.如权利要求5所要求的除草混合物,其中组分A)、组分B)和组分C)以1∶0.1∶0.1 to 1∶50∶10的重量比存在。
8.一种除草组合物,包含除草有效量的如权利要求1-7中任一项所要求的混合物、至少一种惰性液体和/或固体载体和需要的话,至少一种表面活性剂。
9.一种制备如权利要求8所要求的除草组合物的方法,包括将组分A)、组分B)和需要的话,组分C),至少一种惰性液体和/或固体载体以及需要的话,表面活性剂混合。
10.一种防治不希望的植物生长的方法,包括在不希望的植物出苗之前、过程中和/或之后施用如权利要求1-7中任一项所要求的除草混合物,其中组分A)、B)和需要的话,C)可以同时,即联合或单独,或依次施用。
11.如权利要求10所要求的防治不希望的植物生长的方法,其中处理作物植株和不希望的植物的叶子。
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US45397503P | 2003-03-13 | 2003-03-13 | |
US60/453,975 | 2003-03-13 |
Publications (1)
Publication Number | Publication Date |
---|---|
CN1758850A true CN1758850A (zh) | 2006-04-12 |
Family
ID=32990849
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CNA2004800067646A Pending CN1758850A (zh) | 2003-03-13 | 2004-03-12 | 包含Picolinafen的除草混合物 |
Country Status (18)
Country | Link |
---|---|
US (1) | US7846872B2 (zh) |
EP (5) | EP2258189A3 (zh) |
JP (1) | JP5291879B2 (zh) |
KR (1) | KR20050114645A (zh) |
CN (1) | CN1758850A (zh) |
AR (1) | AR043615A1 (zh) |
AU (1) | AU2004220342B2 (zh) |
BR (1) | BRPI0408232A (zh) |
CA (1) | CA2518566C (zh) |
CL (2) | CL2004000523A1 (zh) |
DK (2) | DK2258188T3 (zh) |
EA (1) | EA009959B1 (zh) |
ES (2) | ES2387618T3 (zh) |
MX (1) | MXPA05009115A (zh) |
NZ (1) | NZ542199A (zh) |
PL (2) | PL2258188T3 (zh) |
UA (1) | UA83215C2 (zh) |
WO (1) | WO2004081129A2 (zh) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102919229A (zh) * | 2012-11-26 | 2013-02-13 | 联保作物科技有限公司 | 一种除草组合物 |
CN103281899A (zh) * | 2010-10-27 | 2013-09-04 | 陶氏益农公司 | 包含氯氟吡氧乙酸和二氯喹啉酸的协同性除草组合物 |
CN107771810A (zh) * | 2016-08-30 | 2018-03-09 | 南京华洲药业有限公司 | 一种含麦草畏与氟吡草胺的除草组合物及其应用 |
CN112790192A (zh) * | 2021-02-03 | 2021-05-14 | 安徽润农腾辉生物科技有限公司 | 一种包含氟吡酰草胺的三元除草组合物 |
Families Citing this family (20)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GT200500369A (es) * | 2004-12-17 | 2006-11-07 | Composicion herbicida | |
BE1018402A3 (nl) * | 2009-07-16 | 2010-10-05 | Globachem | Synergie tussen quinmerac, clomazone en diflufenican in herbicide samenstellingen voor het bestrijden van onkruid in land- en tuinbouwgewassen. |
US8338334B2 (en) | 2010-10-27 | 2012-12-25 | Dow Agrosciences, Llc | Synergistic herbicidal composition containing fluroxypyr and quinclorac |
CN102919239A (zh) * | 2012-11-20 | 2013-02-13 | 李福元 | 一种大蒜专用除草剂组合物制剂及其应用 |
AR094004A1 (es) * | 2012-12-18 | 2015-07-01 | Bayer Cropscience Ag | Agentes herbicidas que contienen tri-alato |
RU2650555C2 (ru) | 2013-03-08 | 2018-04-16 | ДАУ АГРОСАЙЕНСИЗ ЭлЭлСи | Гербицидные композиции, содержащие изоксабен и аминопиралид |
US20150099637A1 (en) * | 2013-10-06 | 2015-04-09 | Bomi Framroze | New method to improve the performance of herbicide formulations |
UA123991C2 (uk) | 2015-01-22 | 2021-07-07 | Басф Агро Б.В. | Трикомпонентна гербіцидна комбінація, що включає сафлуфенацил |
KR102549057B1 (ko) | 2015-07-10 | 2023-06-29 | 바스프 아그로 비.브이. | 신메틸린 및 아세토클로르 또는 프레틸라클로르를 포함하는 제초제 조성물 |
US11219215B2 (en) | 2015-07-10 | 2022-01-11 | BASF Agro B.V. | Herbicidal composition comprising cinmethylin and specific inhibitors of protoporphyrinogen oxidase |
WO2017009090A1 (en) | 2015-07-10 | 2017-01-19 | BASF Agro B.V. | Herbicidal composition comprising cinmethylin and pyroxasulfone |
EP3319427B1 (en) | 2015-07-10 | 2019-04-17 | BASF Agro B.V. | Herbicidal composition comprising cinmethylin and dimethenamid |
US20180184659A1 (en) | 2015-07-10 | 2018-07-05 | BASF Agro B.V. | Herbicidal composition comprising cinmethylin and specific pigment synthesis inhibitors |
WO2017009137A1 (en) | 2015-07-10 | 2017-01-19 | BASF Agro B.V. | Herbicidal composition comprising cinmethylinandpethoxamid |
SI3319441T1 (sl) * | 2015-07-10 | 2019-10-30 | Basf Agro Bv | Herbicidni sestavek, ki vsebuje cinmetilin in specifične inhibitorje fitoen desaturaze |
BR112018000482B1 (pt) | 2015-07-10 | 2022-11-22 | BASF Agro B.V. | Composição herbicida, uso da composição e método para o controle da vegetação indesejada |
WO2017009144A1 (en) * | 2015-07-10 | 2017-01-19 | BASF Agro B.V. | Herbicidal composition comprising cinmethylin and specific quinolinecarboxylic acids |
US11219212B2 (en) | 2015-07-10 | 2022-01-11 | BASF Agro B.V. | Herbicidal composition comprising cinmethylin and imazamox |
US11497213B2 (en) * | 2018-09-04 | 2022-11-15 | Purdue Research Foundation | Synergistic effect of isoxaben and cellulosin as a herbicide |
US11938121B2 (en) | 2020-04-15 | 2024-03-26 | Purdue Research Foundation | Treatment of infections and biofilm formation using a cellulose synthase inhibitor |
Family Cites Families (20)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3537840A (en) * | 1967-11-07 | 1970-11-03 | Uniroyal Inc | Synergistic herbicidal composition of sodium n-naphthyl phthalamic acid and 4 - (methylsulfonyl)-2,6-dinitro-n,n-dipropylaniline |
DE2217722C2 (de) | 1972-04-13 | 1982-11-04 | Basf Ag, 6700 Ludwigshafen | Herbizid |
US3884672A (en) * | 1972-09-13 | 1975-05-20 | Gulf Research Development Co | Synergistic chemical control of nutsedge with combination of a 1-methyl-4-phenyl-pyridinium salt and a cyclopropylamino-triazine herbicide |
EP0043349B1 (de) * | 1980-06-27 | 1987-08-12 | Ciba-Geigy Ag | Synergistisches Mittel und Verfahren zur selektiven Unkrautbekämpfung, insbesondere in Getreide und Sojabohnenkulturen |
DE3524319A1 (de) * | 1985-07-08 | 1987-01-08 | Basf Ag | Herbizide und wachstumsregulierende mittel auf basis von chinolinderivaten |
DE3536035A1 (de) * | 1985-10-09 | 1987-04-09 | Hoechst Ag | Herbizide mittel |
EP0230596B1 (en) * | 1985-12-30 | 1992-01-02 | Stauffer Chemical Company | Synergistic herbicide combinations and method of application |
GB8630697D0 (en) * | 1986-12-23 | 1987-02-04 | May & Baker Ltd | Compositions of matter |
FR2625410A1 (fr) * | 1988-01-06 | 1989-07-07 | Rhone Poulenc Agrochimie | Association herbicide synergique a base de bifenox et d'isoxaben |
FR2639185B1 (fr) | 1988-11-22 | 1991-01-25 | Rhone Poulenc Agrochimie | Produit herbicide, son utilisation et procede pour la lutte selective contre les mauvaises herbes dans les cultures de riz et de cereales |
US5665673A (en) * | 1988-12-29 | 1997-09-09 | Anderson; Richard J. | Potentiating herbicidal compositions |
GB9005965D0 (en) | 1990-03-16 | 1990-05-09 | Shell Int Research | Herbicidal carboxamide derivatives |
CN1074646C (zh) * | 1992-10-06 | 2001-11-14 | 国际壳牌研究有限公司 | 除草剂混合物 |
ATE245899T1 (de) * | 1996-03-13 | 2003-08-15 | Syngenta Participations Ag | Herbizide kombinationen |
GB9914213D0 (en) | 1999-06-17 | 1999-08-18 | Rhone Poulenc Agrochimie | New herbicidal compositions |
EE05542B1 (et) | 1999-10-14 | 2012-06-15 | Basf Aktiengesellschaft | Snergilised herbitsiidsed meetodid ja kompositsioonid |
HUP0301968A3 (en) * | 1999-11-17 | 2004-06-28 | Bayer Ag | Selective and synergistic herbicide compositions containing 2,6-disubstituted pyridine derivatives, preparation and use thereof |
EA006848B1 (ru) * | 2000-04-04 | 2006-04-28 | Басф Акциенгезельшафт | Синергетические гербицидные смеси |
US6894003B2 (en) * | 2000-06-23 | 2005-05-17 | Basf Aktiengesellschaft | Enhancement of the activity of carotenoid biosynthesis inhibitor herbicides |
AU2002210461B2 (en) * | 2000-08-25 | 2006-12-14 | Basf Aktiengesellschaft | Herbicidal mixtures |
-
2004
- 2004-03-12 EA EA200501358A patent/EA009959B1/ru not_active IP Right Cessation
- 2004-03-12 MX MXPA05009115A patent/MXPA05009115A/es active IP Right Grant
- 2004-03-12 WO PCT/EP2004/002633 patent/WO2004081129A2/de active Application Filing
- 2004-03-12 US US10/548,841 patent/US7846872B2/en not_active Expired - Fee Related
- 2004-03-12 AU AU2004220342A patent/AU2004220342B2/en not_active Ceased
- 2004-03-12 CA CA2518566A patent/CA2518566C/en not_active Expired - Fee Related
- 2004-03-12 DK DK10175396.0T patent/DK2258188T3/da active
- 2004-03-12 EP EP10175397A patent/EP2258189A3/de not_active Withdrawn
- 2004-03-12 KR KR1020057016846A patent/KR20050114645A/ko not_active Application Discontinuation
- 2004-03-12 DK DK04719990.6T patent/DK1605757T3/da active
- 2004-03-12 ES ES04719990T patent/ES2387618T3/es not_active Expired - Lifetime
- 2004-03-12 EP EP10175396.0A patent/EP2258188B1/de not_active Expired - Lifetime
- 2004-03-12 CN CNA2004800067646A patent/CN1758850A/zh active Pending
- 2004-03-12 EP EP10175393A patent/EP2258187A3/de not_active Withdrawn
- 2004-03-12 EP EP04719990A patent/EP1605757B1/de not_active Expired - Lifetime
- 2004-03-12 BR BRPI0408232-0A patent/BRPI0408232A/pt not_active Application Discontinuation
- 2004-03-12 PL PL10175396T patent/PL2258188T3/pl unknown
- 2004-03-12 CL CL200400523A patent/CL2004000523A1/es unknown
- 2004-03-12 JP JP2006504681A patent/JP5291879B2/ja not_active Expired - Fee Related
- 2004-03-12 EP EP10175390A patent/EP2258186A3/de not_active Withdrawn
- 2004-03-12 NZ NZ542199A patent/NZ542199A/en not_active IP Right Cessation
- 2004-03-12 PL PL04719990T patent/PL1605757T3/pl unknown
- 2004-03-12 ES ES10175396.0T patent/ES2455965T3/es not_active Expired - Lifetime
- 2004-03-15 AR ARP040100857A patent/AR043615A1/es unknown
- 2004-12-03 UA UAA200509526A patent/UA83215C2/uk unknown
-
2009
- 2009-11-17 CL CL2009002097A patent/CL2009002097A1/es unknown
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN103281899A (zh) * | 2010-10-27 | 2013-09-04 | 陶氏益农公司 | 包含氯氟吡氧乙酸和二氯喹啉酸的协同性除草组合物 |
CN103281899B (zh) * | 2010-10-27 | 2015-04-08 | 陶氏益农公司 | 包含氯氟吡氧乙酸和二氯喹啉酸的协同性除草组合物 |
CN102919229A (zh) * | 2012-11-26 | 2013-02-13 | 联保作物科技有限公司 | 一种除草组合物 |
CN102919229B (zh) * | 2012-11-26 | 2014-04-16 | 联保作物科技有限公司 | 一种除草组合物 |
CN107771810A (zh) * | 2016-08-30 | 2018-03-09 | 南京华洲药业有限公司 | 一种含麦草畏与氟吡草胺的除草组合物及其应用 |
CN112790192A (zh) * | 2021-02-03 | 2021-05-14 | 安徽润农腾辉生物科技有限公司 | 一种包含氟吡酰草胺的三元除草组合物 |
Also Published As
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN1758850A (zh) | 包含Picolinafen的除草混合物 | |
CN1206912C (zh) | 异丙甲草胺的增效除草组合物 | |
CN1184886C (zh) | 除草组合物 | |
CN1138762C (zh) | 苯基哒嗪酮 | |
CN1596649A (zh) | 一种含有甲基磺草酮的除草组合物 | |
CN1016484B (zh) | 含取代的四唑啉酮的组合物 | |
CN1158280C (zh) | 取代的噻吩-3-基磺酰基氨基(硫代)羰基三唑啉(硫)酮类化合物 | |
JP6467348B2 (ja) | ALS阻害薬系除草剤耐性テンサイ(Betavulgaris)植物における望ましくない植生を防除するためのALS阻害薬系除草剤の使用 | |
CN1049846A (zh) | 具有除草活性的戊二酰亚胺 | |
CN1198506C (zh) | 除草组合物 | |
CN1787743A (zh) | 协同增效作用的除草混合物 | |
CN1134929A (zh) | 杀真菌方法、化合物和含二苯甲酮的组合物 | |
CN1668197A (zh) | 协同增效作用的除草混合物 | |
CN1668199A (zh) | 协同增效作用的除草混合物 | |
CN1606407A (zh) | 基于7-吡唑基苯并噁唑的除草混合物 | |
CN1074646C (zh) | 除草剂混合物 | |
CN1048852A (zh) | 新的取代的α-嘧啶氧(硫)基-和α-三嗪氧(硫)基羧酸衍生物,它们的制备方法,以及它们作为除草剂,杀菌剂和植物生长调节剂的应用 | |
CN1173112A (zh) | 除草混合物 | |
CN1051287A (zh) | 增效除草剂 | |
CN1537110A (zh) | 制备吡啶化合物的方法 | |
CN1761393A (zh) | 包含安全剂的除草混合物 | |
CN1761394A (zh) | 协同作用的除草混合物 | |
CN1160393A (zh) | N-(邻位取代苄氧基)亚胺衍生物及其用作杀真菌剂、杀螨剂或杀虫剂的用途 | |
CN1787742A (zh) | 除草混合物 | |
CN1370153A (zh) | 新的四唑啉酮衍生物 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
C06 | Publication | ||
PB01 | Publication | ||
C10 | Entry into substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
C02 | Deemed withdrawal of patent application after publication (patent law 2001) | ||
WD01 | Invention patent application deemed withdrawn after publication |