CN101087530A - 杀真菌混合物 - Google Patents
杀真菌混合物 Download PDFInfo
- Publication number
- CN101087530A CN101087530A CNA2005800447391A CN200580044739A CN101087530A CN 101087530 A CN101087530 A CN 101087530A CN A2005800447391 A CNA2005800447391 A CN A2005800447391A CN 200580044739 A CN200580044739 A CN 200580044739A CN 101087530 A CN101087530 A CN 101087530A
- Authority
- CN
- China
- Prior art keywords
- compound
- bacterium
- methyl
- azoles
- mixture
- 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.)
- Granted
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 54
- 230000000855 fungicidal effect Effects 0.000 title claims abstract description 12
- 150000001875 compounds Chemical class 0.000 claims abstract description 244
- -1 cyflufenamides Substances 0.000 claims abstract description 74
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims abstract description 29
- 150000003851 azoles Chemical class 0.000 claims abstract description 21
- 238000000034 method Methods 0.000 claims abstract description 10
- 241000233866 Fungi Species 0.000 claims abstract description 6
- XERJKGMBORTKEO-VZUCSPMQSA-N (1e)-2-(ethylcarbamoylamino)-n-methoxy-2-oxoethanimidoyl cyanide Chemical compound CCNC(=O)NC(=O)C(\C#N)=N\OC XERJKGMBORTKEO-VZUCSPMQSA-N 0.000 claims abstract description 5
- 239000005756 Cymoxanil Substances 0.000 claims abstract description 5
- CJHXCRMKMMBYJQ-UHFFFAOYSA-N dimethirimol Chemical compound CCCCC1=C(C)NC(N(C)C)=NC1=O CJHXCRMKMMBYJQ-UHFFFAOYSA-N 0.000 claims abstract description 5
- CIEXPHRYOLIQQD-UHFFFAOYSA-N methyl N-(2,6-dimethylphenyl)-N-2-furoylalaninate Chemical compound CC=1C=CC=C(C)C=1N(C(C)C(=O)OC)C(=O)C1=CC=CO1 CIEXPHRYOLIQQD-UHFFFAOYSA-N 0.000 claims abstract description 5
- 150000004657 carbamic acid derivatives Chemical class 0.000 claims abstract description 4
- 150000004045 organic chlorine compounds Chemical class 0.000 claims abstract description 4
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims abstract description 3
- 239000005864 Sulphur Substances 0.000 claims abstract description 3
- 125000006501 nitrophenyl group Chemical group 0.000 claims abstract description 3
- 150000002903 organophosphorus compounds Chemical class 0.000 claims abstract description 3
- 241000894006 Bacteria Species 0.000 claims description 50
- 150000001412 amines Chemical class 0.000 claims description 20
- 239000011737 fluorine Substances 0.000 claims description 20
- 229910052731 fluorine Inorganic materials 0.000 claims description 20
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 claims description 15
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 13
- 239000000460 chlorine Substances 0.000 claims description 13
- KAESVJOAVNADME-UHFFFAOYSA-N Pyrrole Chemical compound C=1C=CNC=1 KAESVJOAVNADME-UHFFFAOYSA-N 0.000 claims description 12
- 229910052760 oxygen Inorganic materials 0.000 claims description 12
- 229910052801 chlorine Inorganic materials 0.000 claims description 11
- 229940084434 fungoid Drugs 0.000 claims description 11
- 239000001301 oxygen Substances 0.000 claims description 11
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 10
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims description 9
- 239000005784 Fluoxastrobin Substances 0.000 claims description 9
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 9
- UFEODZBUAFNAEU-NLRVBDNBSA-N fluoxastrobin Chemical compound C=1C=CC=C(OC=2C(=C(OC=3C(=CC=CC=3)Cl)N=CN=2)F)C=1C(=N/OC)\C1=NOCCO1 UFEODZBUAFNAEU-NLRVBDNBSA-N 0.000 claims description 9
- 238000002360 preparation method Methods 0.000 claims description 9
- YTPLMLYBLZKORZ-UHFFFAOYSA-N Thiophene Chemical compound C=1C=CSC=1 YTPLMLYBLZKORZ-UHFFFAOYSA-N 0.000 claims description 8
- FPIPGXGPPPQFEQ-OVSJKPMPSA-N all-trans-retinol Chemical compound OC\C=C(/C)\C=C\C=C(/C)\C=C\C1=C(C)CCCC1(C)C FPIPGXGPPPQFEQ-OVSJKPMPSA-N 0.000 claims description 8
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 8
- UZCGKGPEKUCDTF-UHFFFAOYSA-N fluazinam Chemical compound [O-][N+](=O)C1=CC(C(F)(F)F)=C(Cl)C([N+]([O-])=O)=C1NC1=NC=C(C(F)(F)F)C=C1Cl UZCGKGPEKUCDTF-UHFFFAOYSA-N 0.000 claims description 8
- 229910052739 hydrogen Inorganic materials 0.000 claims description 8
- 239000001257 hydrogen Substances 0.000 claims description 8
- 150000002825 nitriles Chemical class 0.000 claims description 8
- JMANVNJQNLATNU-UHFFFAOYSA-N oxalonitrile Chemical compound N#CC#N JMANVNJQNLATNU-UHFFFAOYSA-N 0.000 claims description 8
- UCSJYZPVAKXKNQ-HZYVHMACSA-N streptomycin Chemical compound CN[C@H]1[C@H](O)[C@@H](O)[C@H](CO)O[C@H]1O[C@@H]1[C@](C=O)(O)[C@H](C)O[C@H]1O[C@@H]1[C@@H](NC(N)=N)[C@H](O)[C@@H](NC(N)=N)[C@H](O)[C@H]1O UCSJYZPVAKXKNQ-HZYVHMACSA-N 0.000 claims description 8
- PZBPKYOVPCNPJY-UHFFFAOYSA-N 1-[2-(allyloxy)-2-(2,4-dichlorophenyl)ethyl]imidazole Chemical compound ClC1=CC(Cl)=CC=C1C(OCC=C)CN1C=NC=C1 PZBPKYOVPCNPJY-UHFFFAOYSA-N 0.000 claims description 7
- 239000005780 Fluazinam Substances 0.000 claims description 7
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 7
- UDSJPFPDKCMYBD-UHFFFAOYSA-N Metsulfovax Chemical compound S1C(C)=NC(C)=C1C(=O)NC1=CC=CC=C1 UDSJPFPDKCMYBD-UHFFFAOYSA-N 0.000 claims description 7
- CZPWVGJYEJSRLH-UHFFFAOYSA-N Pyrimidine Chemical compound C1=CN=CN=C1 CZPWVGJYEJSRLH-UHFFFAOYSA-N 0.000 claims description 7
- 239000002253 acid Substances 0.000 claims description 7
- WYEMLYFITZORAB-UHFFFAOYSA-N boscalid Chemical compound C1=CC(Cl)=CC=C1C1=CC=CC=C1NC(=O)C1=CC=CN=C1Cl WYEMLYFITZORAB-UHFFFAOYSA-N 0.000 claims description 7
- HZRSNVGNWUDEFX-UHFFFAOYSA-N pyraclostrobin Chemical compound COC(=O)N(OC)C1=CC=CC=C1COC1=NN(C=2C=CC(Cl)=CC=2)C=C1 HZRSNVGNWUDEFX-UHFFFAOYSA-N 0.000 claims description 7
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 claims description 7
- QNBTYORWCCMPQP-JXAWBTAJSA-N (Z)-dimethomorph Chemical compound C1=C(OC)C(OC)=CC=C1C(\C=1C=CC(Cl)=CC=1)=C/C(=O)N1CCOCC1 QNBTYORWCCMPQP-JXAWBTAJSA-N 0.000 claims description 6
- 125000004207 3-methoxyphenyl group Chemical group [H]C1=C([H])C(*)=C([H])C(OC([H])([H])[H])=C1[H] 0.000 claims description 6
- 239000005740 Boscalid Substances 0.000 claims description 6
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 claims description 6
- YLQBMQCUIZJEEH-UHFFFAOYSA-N Furan Chemical compound C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 claims description 6
- 239000005795 Imazalil Substances 0.000 claims description 6
- 239000005802 Mancozeb Substances 0.000 claims description 6
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 claims description 6
- 239000005869 Pyraclostrobin Substances 0.000 claims description 6
- CHFKUVPQTICASN-UHFFFAOYSA-N [O]CC#C Chemical compound [O]CC#C CHFKUVPQTICASN-UHFFFAOYSA-N 0.000 claims description 6
- 229940118790 boscalid Drugs 0.000 claims description 6
- PYZSVQVRHDXQSL-UHFFFAOYSA-N dithianon Chemical compound S1C(C#N)=C(C#N)SC2=C1C(=O)C1=CC=CC=C1C2=O PYZSVQVRHDXQSL-UHFFFAOYSA-N 0.000 claims description 6
- 229960002125 enilconazole Drugs 0.000 claims description 6
- WDQNIWFZKXZFAY-UHFFFAOYSA-M fentin acetate Chemical compound CC([O-])=O.C1=CC=CC=C1[Sn+](C=1C=CC=CC=1)C1=CC=CC=C1 WDQNIWFZKXZFAY-UHFFFAOYSA-M 0.000 claims description 6
- 150000002466 imines Chemical class 0.000 claims description 6
- ZQEIXNIJLIKNTD-UHFFFAOYSA-N methyl N-(2,6-dimethylphenyl)-N-(methoxyacetyl)alaninate Chemical compound COCC(=O)N(C(C)C(=O)OC)C1=C(C)C=CC=C1C ZQEIXNIJLIKNTD-UHFFFAOYSA-N 0.000 claims description 6
- 230000002195 synergetic effect Effects 0.000 claims description 6
- HYVWIQDYBVKITD-UHFFFAOYSA-N tolylfluanid Chemical compound CN(C)S(=O)(=O)N(SC(F)(Cl)Cl)C1=CC=C(C)C=C1 HYVWIQDYBVKITD-UHFFFAOYSA-N 0.000 claims description 6
- LDVVMCZRFWMZSG-OLQVQODUSA-N (3ar,7as)-2-(trichloromethylsulfanyl)-3a,4,7,7a-tetrahydroisoindole-1,3-dione Chemical compound C1C=CC[C@H]2C(=O)N(SC(Cl)(Cl)Cl)C(=O)[C@H]21 LDVVMCZRFWMZSG-OLQVQODUSA-N 0.000 claims description 5
- JWUCHKBSVLQQCO-UHFFFAOYSA-N 1-(2-fluorophenyl)-1-(4-fluorophenyl)-2-(1H-1,2,4-triazol-1-yl)ethanol Chemical compound C=1C=C(F)C=CC=1C(C=1C(=CC=CC=1)F)(O)CN1C=NC=N1 JWUCHKBSVLQQCO-UHFFFAOYSA-N 0.000 claims description 5
- PXMNMQRDXWABCY-UHFFFAOYSA-N 1-(4-chlorophenyl)-4,4-dimethyl-3-(1H-1,2,4-triazol-1-ylmethyl)pentan-3-ol Chemical compound C1=NC=NN1CC(O)(C(C)(C)C)CCC1=CC=C(Cl)C=C1 PXMNMQRDXWABCY-UHFFFAOYSA-N 0.000 claims description 5
- MGNFYQILYYYUBS-UHFFFAOYSA-N 1-[3-(4-tert-butylphenyl)-2-methylpropyl]piperidine Chemical compound C=1C=C(C(C)(C)C)C=CC=1CC(C)CN1CCCCC1 MGNFYQILYYYUBS-UHFFFAOYSA-N 0.000 claims description 5
- YTOPFCCWCSOHFV-UHFFFAOYSA-N 2,6-dimethyl-4-tridecylmorpholine Chemical compound CCCCCCCCCCCCCN1CC(C)OC(C)C1 YTOPFCCWCSOHFV-UHFFFAOYSA-N 0.000 claims description 5
- UFNOUKDBUJZYDE-UHFFFAOYSA-N 2-(4-chlorophenyl)-3-cyclopropyl-1-(1H-1,2,4-triazol-1-yl)butan-2-ol Chemical compound C1=NC=NN1CC(O)(C=1C=CC(Cl)=CC=1)C(C)C1CC1 UFNOUKDBUJZYDE-UHFFFAOYSA-N 0.000 claims description 5
- ZRDUSMYWDRPZRM-UHFFFAOYSA-N 2-sec-butyl-4,6-dinitrophenyl 3-methylbut-2-enoate Chemical compound CCC(C)C1=CC([N+]([O-])=O)=CC([N+]([O-])=O)=C1OC(=O)C=C(C)C ZRDUSMYWDRPZRM-UHFFFAOYSA-N 0.000 claims description 5
- SOUGWDPPRBKJEX-UHFFFAOYSA-N 3,5-dichloro-N-(1-chloro-3-methyl-2-oxopentan-3-yl)-4-methylbenzamide Chemical compound ClCC(=O)C(C)(CC)NC(=O)C1=CC(Cl)=C(C)C(Cl)=C1 SOUGWDPPRBKJEX-UHFFFAOYSA-N 0.000 claims description 5
- FSCWZHGZWWDELK-UHFFFAOYSA-N 3-(3,5-dichlorophenyl)-5-ethenyl-5-methyl-2,4-oxazolidinedione Chemical compound O=C1C(C)(C=C)OC(=O)N1C1=CC(Cl)=CC(Cl)=C1 FSCWZHGZWWDELK-UHFFFAOYSA-N 0.000 claims description 5
- NNPRCLUGHFXSOU-UHFFFAOYSA-N 4-chloro-n-[cyano(ethoxy)methyl]benzamide Chemical compound CCOC(C#N)NC(=O)C1=CC=C(Cl)C=C1 NNPRCLUGHFXSOU-UHFFFAOYSA-N 0.000 claims description 5
- 239000005745 Captan Substances 0.000 claims description 5
- TWFZGCMQGLPBSX-UHFFFAOYSA-N Carbendazim Natural products C1=CC=C2NC(NC(=O)OC)=NC2=C1 TWFZGCMQGLPBSX-UHFFFAOYSA-N 0.000 claims description 5
- 239000005757 Cyproconazole Substances 0.000 claims description 5
- 239000005761 Dimethomorph Substances 0.000 claims description 5
- HDWLUGYOLUHEMN-UHFFFAOYSA-N Dinobuton Chemical compound CCC(C)C1=CC([N+]([O-])=O)=CC([N+]([O-])=O)=C1OC(=O)OC(C)C HDWLUGYOLUHEMN-UHFFFAOYSA-N 0.000 claims description 5
- 239000005776 Fenhexamid Substances 0.000 claims description 5
- 239000005789 Folpet Substances 0.000 claims description 5
- 239000005805 Mepanipyrim Substances 0.000 claims description 5
- 239000005807 Metalaxyl Substances 0.000 claims description 5
- 239000005823 Propineb Substances 0.000 claims description 5
- 239000005828 Pyrimethanil Substances 0.000 claims description 5
- 239000005839 Tebuconazole Substances 0.000 claims description 5
- RIOXQFHNBCKOKP-UHFFFAOYSA-N benomyl Chemical compound C1=CC=C2N(C(=O)NCCCC)C(NC(=O)OC)=NC2=C1 RIOXQFHNBCKOKP-UHFFFAOYSA-N 0.000 claims description 5
- MITFXPHMIHQXPI-UHFFFAOYSA-N benzoxaprofen Natural products N=1C2=CC(C(C(O)=O)C)=CC=C2OC=1C1=CC=C(Cl)C=C1 MITFXPHMIHQXPI-UHFFFAOYSA-N 0.000 claims description 5
- 229940117949 captan Drugs 0.000 claims description 5
- 239000006013 carbendazim Substances 0.000 claims description 5
- JNPZQRQPIHJYNM-UHFFFAOYSA-N carbendazim Chemical compound C1=C[CH]C2=NC(NC(=O)OC)=NC2=C1 JNPZQRQPIHJYNM-UHFFFAOYSA-N 0.000 claims description 5
- KXDHJXZQYSOELW-UHFFFAOYSA-N carbonic acid monoamide Natural products NC(O)=O KXDHJXZQYSOELW-UHFFFAOYSA-N 0.000 claims description 5
- WURGXGVFSMYFCG-UHFFFAOYSA-N dichlofluanid Chemical compound CN(C)S(=O)(=O)N(SC(F)(Cl)Cl)C1=CC=CC=C1 WURGXGVFSMYFCG-UHFFFAOYSA-N 0.000 claims description 5
- VDLGAVXLJYLFDH-UHFFFAOYSA-N fenhexamid Chemical compound C=1C=C(O)C(Cl)=C(Cl)C=1NC(=O)C1(C)CCCCC1 VDLGAVXLJYLFDH-UHFFFAOYSA-N 0.000 claims description 5
- WHDGWKAJBYRJJL-UHFFFAOYSA-K ferbam Chemical compound [Fe+3].CN(C)C([S-])=S.CN(C)C([S-])=S.CN(C)C([S-])=S WHDGWKAJBYRJJL-UHFFFAOYSA-K 0.000 claims description 5
- HKIOYBQGHSTUDB-UHFFFAOYSA-N folpet Chemical compound C1=CC=C2C(=O)N(SC(Cl)(Cl)Cl)C(=O)C2=C1 HKIOYBQGHSTUDB-UHFFFAOYSA-N 0.000 claims description 5
- UYJUZNLFJAWNEZ-UHFFFAOYSA-N fuberidazole Chemical compound C1=COC(C=2NC3=CC=CC=C3N=2)=C1 UYJUZNLFJAWNEZ-UHFFFAOYSA-N 0.000 claims description 5
- RONFGUROBZGJKP-UHFFFAOYSA-N iminoctadine Chemical compound NC(N)=NCCCCCCCCNCCCCCCCCN=C(N)N RONFGUROBZGJKP-UHFFFAOYSA-N 0.000 claims description 5
- UFHLMYOGRXOCSL-UHFFFAOYSA-N isoprothiolane Chemical compound CC(C)OC(=O)C(C(=O)OC(C)C)=C1SCCS1 UFHLMYOGRXOCSL-UHFFFAOYSA-N 0.000 claims description 5
- 150000002576 ketones Chemical class 0.000 claims description 5
- CIFWZNRJIBNXRE-UHFFFAOYSA-N mepanipyrim Chemical compound CC#CC1=CC(C)=NC(NC=2C=CC=CC=2)=N1 CIFWZNRJIBNXRE-UHFFFAOYSA-N 0.000 claims description 5
- CJPQIRJHIZUAQP-UHFFFAOYSA-N methyl N-(2,6-dimethylphenyl)-N-(phenylacetyl)alaninate Chemical compound CC=1C=CC=C(C)C=1N(C(C)C(=O)OC)C(=O)CC1=CC=CC=C1 CJPQIRJHIZUAQP-UHFFFAOYSA-N 0.000 claims description 5
- AMSPWOYQQAWRRM-UHFFFAOYSA-N metrafenone Chemical compound COC1=CC=C(Br)C(C)=C1C(=O)C1=C(C)C=C(OC)C(OC)=C1OC AMSPWOYQQAWRRM-UHFFFAOYSA-N 0.000 claims description 5
- 229910052757 nitrogen Inorganic materials 0.000 claims description 5
- WBTYBAGIHOISOQ-UHFFFAOYSA-N pent-4-en-1-yl 2-[(2-furylmethyl)(imidazol-1-ylcarbonyl)amino]butanoate Chemical compound C1=CN=CN1C(=O)N(C(CC)C(=O)OCCCC=C)CC1=CC=CO1 WBTYBAGIHOISOQ-UHFFFAOYSA-N 0.000 claims description 5
- WHHIPMZEDGBUCC-UHFFFAOYSA-N probenazole Chemical compound C1=CC=C2C(OCC=C)=NS(=O)(=O)C2=C1 WHHIPMZEDGBUCC-UHFFFAOYSA-N 0.000 claims description 5
- KKMLIVYBGSAJPM-UHFFFAOYSA-L propineb Chemical compound [Zn+2].[S-]C(=S)NC(C)CNC([S-])=S KKMLIVYBGSAJPM-UHFFFAOYSA-L 0.000 claims description 5
- ZLIBICFPKPWGIZ-UHFFFAOYSA-N pyrimethanil Chemical compound CC1=CC(C)=NC(NC=2C=CC=CC=2)=N1 ZLIBICFPKPWGIZ-UHFFFAOYSA-N 0.000 claims description 5
- 150000003839 salts Chemical class 0.000 claims description 5
- 239000002689 soil Substances 0.000 claims description 5
- 239000007787 solid Substances 0.000 claims description 5
- KJAMZCVTJDTESW-UHFFFAOYSA-N tiracizine Chemical compound C1CC2=CC=CC=C2N(C(=O)CN(C)C)C2=CC(NC(=O)OCC)=CC=C21 KJAMZCVTJDTESW-UHFFFAOYSA-N 0.000 claims description 5
- NHOWDZOIZKMVAI-UHFFFAOYSA-N (2-chlorophenyl)(4-chlorophenyl)pyrimidin-5-ylmethanol Chemical compound C=1N=CN=CC=1C(C=1C(=CC=CC=1)Cl)(O)C1=CC=C(Cl)C=C1 NHOWDZOIZKMVAI-UHFFFAOYSA-N 0.000 claims description 4
- SAPGTCDSBGMXCD-UHFFFAOYSA-N (2-chlorophenyl)-(4-fluorophenyl)-pyrimidin-5-ylmethanol Chemical compound C=1N=CN=CC=1C(C=1C(=CC=CC=1)Cl)(O)C1=CC=C(F)C=C1 SAPGTCDSBGMXCD-UHFFFAOYSA-N 0.000 claims description 4
- PPDBOQMNKNNODG-NTEUORMPSA-N (5E)-5-(4-chlorobenzylidene)-2,2-dimethyl-1-(1,2,4-triazol-1-ylmethyl)cyclopentanol Chemical compound C1=NC=NN1CC1(O)C(C)(C)CC\C1=C/C1=CC=C(Cl)C=C1 PPDBOQMNKNNODG-NTEUORMPSA-N 0.000 claims description 4
- BKBSMMUEEAWFRX-NBVRZTHBSA-N (E)-flumorph Chemical compound C1=C(OC)C(OC)=CC=C1C(\C=1C=CC(F)=CC=1)=C\C(=O)N1CCOCC1 BKBSMMUEEAWFRX-NBVRZTHBSA-N 0.000 claims description 4
- CKPCAYZTYMHQEX-NBVRZTHBSA-N (e)-1-(2,4-dichlorophenyl)-n-methoxy-2-pyridin-3-ylethanimine Chemical compound C=1C=C(Cl)C=C(Cl)C=1C(=N/OC)/CC1=CC=CN=C1 CKPCAYZTYMHQEX-NBVRZTHBSA-N 0.000 claims description 4
- VGPIBGGRCVEHQZ-UHFFFAOYSA-N 1-(biphenyl-4-yloxy)-3,3-dimethyl-1-(1,2,4-triazol-1-yl)butan-2-ol Chemical compound C1=NC=NN1C(C(O)C(C)(C)C)OC(C=C1)=CC=C1C1=CC=CC=C1 VGPIBGGRCVEHQZ-UHFFFAOYSA-N 0.000 claims description 4
- WKBPZYKAUNRMKP-UHFFFAOYSA-N 1-[2-(2,4-dichlorophenyl)pentyl]1,2,4-triazole Chemical compound C=1C=C(Cl)C=C(Cl)C=1C(CCC)CN1C=NC=N1 WKBPZYKAUNRMKP-UHFFFAOYSA-N 0.000 claims description 4
- YIKWKLYQRFRGPM-UHFFFAOYSA-N 1-dodecylguanidine acetate Chemical compound CC(O)=O.CCCCCCCCCCCCN=C(N)N YIKWKLYQRFRGPM-UHFFFAOYSA-N 0.000 claims description 4
- RQDJADAKIFFEKQ-UHFFFAOYSA-N 4-(4-chlorophenyl)-2-phenyl-2-(1,2,4-triazol-1-ylmethyl)butanenitrile Chemical compound C1=CC(Cl)=CC=C1CCC(C=1C=CC=CC=1)(C#N)CN1N=CN=C1 RQDJADAKIFFEKQ-UHFFFAOYSA-N 0.000 claims description 4
- PCCSBWNGDMYFCW-UHFFFAOYSA-N 5-methyl-5-(4-phenoxyphenyl)-3-(phenylamino)-1,3-oxazolidine-2,4-dione Chemical compound O=C1C(C)(C=2C=CC(OC=3C=CC=CC=3)=CC=2)OC(=O)N1NC1=CC=CC=C1 PCCSBWNGDMYFCW-UHFFFAOYSA-N 0.000 claims description 4
- 239000005741 Bromuconazole Substances 0.000 claims description 4
- 239000005746 Carboxin Substances 0.000 claims description 4
- 239000005755 Cyflufenamid Substances 0.000 claims description 4
- 239000005644 Dazomet Substances 0.000 claims description 4
- 239000005766 Dodine Substances 0.000 claims description 4
- 239000005772 Famoxadone Substances 0.000 claims description 4
- 239000005774 Fenamidone Substances 0.000 claims description 4
- 239000005777 Fenpropidin Substances 0.000 claims description 4
- 239000005785 Fluquinconazole Substances 0.000 claims description 4
- 239000005786 Flutolanil Substances 0.000 claims description 4
- 239000005787 Flutriafol Substances 0.000 claims description 4
- 239000005790 Fosetyl Substances 0.000 claims description 4
- 239000005797 Iprovalicarb Substances 0.000 claims description 4
- NWUWYYSKZYIQAE-ZBFHGGJFSA-N L-(R)-iprovalicarb Chemical compound CC(C)OC(=O)N[C@@H](C(C)C)C(=O)N[C@H](C)C1=CC=C(C)C=C1 NWUWYYSKZYIQAE-ZBFHGGJFSA-N 0.000 claims description 4
- 239000005804 Mandipropamid Substances 0.000 claims description 4
- 239000005810 Metrafenone Substances 0.000 claims description 4
- 239000005813 Penconazole Substances 0.000 claims description 4
- 239000005814 Pencycuron Substances 0.000 claims description 4
- 239000005820 Prochloraz Substances 0.000 claims description 4
- 239000005822 Propiconazole Substances 0.000 claims description 4
- 239000005831 Quinoxyfen Substances 0.000 claims description 4
- 229930182692 Strobilurin Natural products 0.000 claims description 4
- 239000005842 Thiophanate-methyl Substances 0.000 claims description 4
- 239000005846 Triadimenol Substances 0.000 claims description 4
- 239000005859 Triticonazole Substances 0.000 claims description 4
- 239000005870 Ziram Substances 0.000 claims description 4
- 239000005863 Zoxamide Substances 0.000 claims description 4
- 239000011717 all-trans-retinol Substances 0.000 claims description 4
- 235000019169 all-trans-retinol Nutrition 0.000 claims description 4
- 150000001408 amides Chemical class 0.000 claims description 4
- IMHBYKMAHXWHRP-UHFFFAOYSA-N anilazine Chemical compound ClC1=CC=CC=C1NC1=NC(Cl)=NC(Cl)=N1 IMHBYKMAHXWHRP-UHFFFAOYSA-N 0.000 claims description 4
- HJJVPARKXDDIQD-UHFFFAOYSA-N bromuconazole Chemical compound ClC1=CC(Cl)=CC=C1C1(CN2N=CN=C2)OCC(Br)C1 HJJVPARKXDDIQD-UHFFFAOYSA-N 0.000 claims description 4
- GYSSRZJIHXQEHQ-UHFFFAOYSA-N carboxin Chemical compound S1CCOC(C)=C1C(=O)NC1=CC=CC=C1 GYSSRZJIHXQEHQ-UHFFFAOYSA-N 0.000 claims description 4
- ACMXQHFNODYQAT-UHFFFAOYSA-N cyflufenamid Chemical compound FC1=CC=C(C(F)(F)F)C(C(NOCC2CC2)=NC(=O)CC=2C=CC=CC=2)=C1F ACMXQHFNODYQAT-UHFFFAOYSA-N 0.000 claims description 4
- QAYICIQNSGETAS-UHFFFAOYSA-N dazomet Chemical compound CN1CSC(=S)N(C)C1 QAYICIQNSGETAS-UHFFFAOYSA-N 0.000 claims description 4
- UWQMKVBQKFHLCE-UHFFFAOYSA-N diclomezine Chemical compound C1=C(Cl)C(C)=C(Cl)C=C1C1=NNC(=O)C=C1 UWQMKVBQKFHLCE-UHFFFAOYSA-N 0.000 claims description 4
- AWZOLILCOUMRDG-UHFFFAOYSA-N edifenphos Chemical compound C=1C=CC=CC=1SP(=O)(OCC)SC1=CC=CC=C1 AWZOLILCOUMRDG-UHFFFAOYSA-N 0.000 claims description 4
- VMNULHCTRPXWFJ-UJSVPXBISA-N enoxastrobin Chemical compound CO\C=C(\C(=O)OC)C1=CC=CC=C1CO\N=C(/C)\C=C\C1=CC=C(Cl)C=C1 VMNULHCTRPXWFJ-UJSVPXBISA-N 0.000 claims description 4
- 150000002148 esters Chemical class 0.000 claims description 4
- LMVPQMGRYSRMIW-KRWDZBQOSA-N fenamidone Chemical compound O=C([C@@](C)(N=C1SC)C=2C=CC=CC=2)N1NC1=CC=CC=C1 LMVPQMGRYSRMIW-KRWDZBQOSA-N 0.000 claims description 4
- FKLFBQCQQYDUAM-UHFFFAOYSA-N fenpiclonil Chemical compound ClC1=CC=CC(C=2C(=CNC=2)C#N)=C1Cl FKLFBQCQQYDUAM-UHFFFAOYSA-N 0.000 claims description 4
- GOWLARCWZRESHU-AQTBWJFISA-N ferimzone Chemical compound C=1C=CC=C(C)C=1C(/C)=N\NC1=NC(C)=CC(C)=N1 GOWLARCWZRESHU-AQTBWJFISA-N 0.000 claims description 4
- IJJVMEJXYNJXOJ-UHFFFAOYSA-N fluquinconazole Chemical compound C=1C=C(Cl)C=C(Cl)C=1N1C(=O)C2=CC(F)=CC=C2N=C1N1C=NC=N1 IJJVMEJXYNJXOJ-UHFFFAOYSA-N 0.000 claims description 4
- FQKUGOMFVDPBIZ-UHFFFAOYSA-N flusilazole Chemical compound C=1C=C(F)C=CC=1[Si](C=1C=CC(F)=CC=1)(C)CN1C=NC=N1 FQKUGOMFVDPBIZ-UHFFFAOYSA-N 0.000 claims description 4
- GNVDAZSPJWCIQZ-UHFFFAOYSA-N flusulfamide Chemical compound ClC1=CC([N+](=O)[O-])=CC=C1NS(=O)(=O)C1=CC=C(Cl)C(C(F)(F)F)=C1 GNVDAZSPJWCIQZ-UHFFFAOYSA-N 0.000 claims description 4
- PTCGDEVVHUXTMP-UHFFFAOYSA-N flutolanil Chemical compound CC(C)OC1=CC=CC(NC(=O)C=2C(=CC=CC=2)C(F)(F)F)=C1 PTCGDEVVHUXTMP-UHFFFAOYSA-N 0.000 claims description 4
- VUERQRKTYBIULR-UHFFFAOYSA-N fosetyl Chemical compound CCOP(O)=O VUERQRKTYBIULR-UHFFFAOYSA-N 0.000 claims description 4
- 239000000417 fungicide Substances 0.000 claims description 4
- CKAPSXZOOQJIBF-UHFFFAOYSA-N hexachlorobenzene Chemical compound ClC1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1Cl CKAPSXZOOQJIBF-UHFFFAOYSA-N 0.000 claims description 4
- KGVPNLBXJKTABS-UHFFFAOYSA-N hymexazol Chemical compound CC1=CC(O)=NO1 KGVPNLBXJKTABS-UHFFFAOYSA-N 0.000 claims description 4
- FCOAHACKGGIURQ-UHFFFAOYSA-N iprobenfos Chemical compound CC(C)OP(=O)(OC(C)C)SCC1=CC=CC=C1 FCOAHACKGGIURQ-UHFFFAOYSA-N 0.000 claims description 4
- YKSNLCVSTHTHJA-UHFFFAOYSA-L maneb Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S YKSNLCVSTHTHJA-UHFFFAOYSA-L 0.000 claims description 4
- 229920000940 maneb Polymers 0.000 claims description 4
- ZQEIXNIJLIKNTD-GFCCVEGCSA-N metalaxyl-M Chemical compound COCC(=O)N([C@H](C)C(=O)OC)C1=C(C)C=CC=C1C ZQEIXNIJLIKNTD-GFCCVEGCSA-N 0.000 claims description 4
- JHIPUJPTQJYEQK-ZLHHXESBSA-N orysastrobin Chemical compound CNC(=O)C(=N\OC)\C1=CC=CC=C1CO\N=C(/C)\C(=N\OC)\C(\C)=N\OC JHIPUJPTQJYEQK-ZLHHXESBSA-N 0.000 claims description 4
- 150000002923 oximes Chemical class 0.000 claims description 4
- AMEKQAFGQBKLKX-UHFFFAOYSA-N oxycarboxin Chemical compound O=S1(=O)CCOC(C)=C1C(=O)NC1=CC=CC=C1 AMEKQAFGQBKLKX-UHFFFAOYSA-N 0.000 claims description 4
- OGYFATSSENRIKG-UHFFFAOYSA-N pencycuron Chemical compound C1=CC(Cl)=CC=C1CN(C(=O)NC=1C=CC=CC=1)C1CCCC1 OGYFATSSENRIKG-UHFFFAOYSA-N 0.000 claims description 4
- TVLSRXXIMLFWEO-UHFFFAOYSA-N prochloraz Chemical compound C1=CN=CN1C(=O)N(CCC)CCOC1=C(Cl)C=C(Cl)C=C1Cl TVLSRXXIMLFWEO-UHFFFAOYSA-N 0.000 claims description 4
- STJLVHWMYQXCPB-UHFFFAOYSA-N propiconazole Chemical compound O1C(CCC)COC1(C=1C(=CC(Cl)=CC=1)Cl)CN1N=CN=C1 STJLVHWMYQXCPB-UHFFFAOYSA-N 0.000 claims description 4
- XRJLAOUDSILTFT-UHFFFAOYSA-N pyroquilon Chemical compound O=C1CCC2=CC=CC3=C2N1CC3 XRJLAOUDSILTFT-UHFFFAOYSA-N 0.000 claims description 4
- WRPIRSINYZBGPK-UHFFFAOYSA-N quinoxyfen Chemical compound C1=CC(F)=CC=C1OC1=CC=NC2=CC(Cl)=CC(Cl)=C12 WRPIRSINYZBGPK-UHFFFAOYSA-N 0.000 claims description 4
- 230000001954 sterilising effect Effects 0.000 claims description 4
- 238000004659 sterilization and disinfection Methods 0.000 claims description 4
- 229960005322 streptomycin Drugs 0.000 claims description 4
- 239000004308 thiabendazole Substances 0.000 claims description 4
- WJCNZQLZVWNLKY-UHFFFAOYSA-N thiabendazole Chemical compound S1C=NC(C=2NC3=CC=CC=C3N=2)=C1 WJCNZQLZVWNLKY-UHFFFAOYSA-N 0.000 claims description 4
- 235000010296 thiabendazole Nutrition 0.000 claims description 4
- 229960004546 thiabendazole Drugs 0.000 claims description 4
- WOSNCVAPUOFXEH-UHFFFAOYSA-N thifluzamide Chemical compound S1C(C)=NC(C(F)(F)F)=C1C(=O)NC1=C(Br)C=C(OC(F)(F)F)C=C1Br WOSNCVAPUOFXEH-UHFFFAOYSA-N 0.000 claims description 4
- QGHREAKMXXNCOA-UHFFFAOYSA-N thiophanate-methyl Chemical group COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC QGHREAKMXXNCOA-UHFFFAOYSA-N 0.000 claims description 4
- 229930192474 thiophene Natural products 0.000 claims description 4
- VJQYLJSMBWXGDV-UHFFFAOYSA-N tiadinil Chemical compound N1=NSC(C(=O)NC=2C=C(Cl)C(C)=CC=2)=C1C VJQYLJSMBWXGDV-UHFFFAOYSA-N 0.000 claims description 4
- BAZVSMNPJJMILC-UHFFFAOYSA-N triadimenol Chemical compound C1=NC=NN1C(C(O)C(C)(C)C)OC1=CC=C(Cl)C=C1 BAZVSMNPJJMILC-UHFFFAOYSA-N 0.000 claims description 4
- DQJCHOQLCLEDLL-UHFFFAOYSA-N tricyclazole Chemical compound CC1=CC=CC2=C1N1C=NN=C1S2 DQJCHOQLCLEDLL-UHFFFAOYSA-N 0.000 claims description 4
- RROQIUMZODEXOR-UHFFFAOYSA-N triforine Chemical compound O=CNC(C(Cl)(Cl)Cl)N1CCN(C(NC=O)C(Cl)(Cl)Cl)CC1 RROQIUMZODEXOR-UHFFFAOYSA-N 0.000 claims description 4
- DUBNHZYBDBBJHD-UHFFFAOYSA-L ziram Chemical compound [Zn+2].CN(C)C([S-])=S.CN(C)C([S-])=S DUBNHZYBDBBJHD-UHFFFAOYSA-L 0.000 claims description 4
- RNSKZDUUNLMFJL-UHFFFAOYSA-N 1,2-thiazole-5-carboxamide Chemical compound NC(=O)C1=CC=NS1 RNSKZDUUNLMFJL-UHFFFAOYSA-N 0.000 claims description 3
- NMWKWBPNKPGATC-UHFFFAOYSA-N 4,5,6,7-tetrachloro-2-benzofuran-1(3H)-one Chemical compound ClC1=C(Cl)C(Cl)=C2COC(=O)C2=C1Cl NMWKWBPNKPGATC-UHFFFAOYSA-N 0.000 claims description 3
- YLJLLELGHSWIDU-UHFFFAOYSA-N 4-cyclododecyl-2,6-dimethylmorpholin-4-ium;acetate Chemical compound CC([O-])=O.C1C(C)OC(C)C[NH+]1C1CCCCCCCCCCC1 YLJLLELGHSWIDU-UHFFFAOYSA-N 0.000 claims description 3
- BIHPYCDDPGNWQO-UHFFFAOYSA-N 5-iai Chemical compound C1=C(I)C=C2CC(N)CC2=C1 BIHPYCDDPGNWQO-UHFFFAOYSA-N 0.000 claims description 3
- XNCOSPRUTUOJCJ-UHFFFAOYSA-N Biguanide Chemical compound NC(N)=NC(N)=N XNCOSPRUTUOJCJ-UHFFFAOYSA-N 0.000 claims description 3
- 229940123208 Biguanide Drugs 0.000 claims description 3
- 239000005739 Bordeaux mixture Substances 0.000 claims description 3
- UMIVDQOVSJFWOH-UHFFFAOYSA-N C1(=CC=CC=C1)C1=CC=CC=C1.[F] Chemical group C1(=CC=CC=C1)C1=CC=CC=C1.[F] UMIVDQOVSJFWOH-UHFFFAOYSA-N 0.000 claims description 3
- 239000005808 Metalaxyl-M Substances 0.000 claims description 3
- RJUFJBKOKNCXHH-UHFFFAOYSA-N Methyl propionate Chemical compound CCC(=O)OC RJUFJBKOKNCXHH-UHFFFAOYSA-N 0.000 claims description 3
- 229930182764 Polyoxin Natural products 0.000 claims description 3
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims description 3
- WHDHEVMINMZADQ-UHFFFAOYSA-N [F].N1C=CC=C1 Chemical compound [F].N1C=CC=C1 WHDHEVMINMZADQ-UHFFFAOYSA-N 0.000 claims description 3
- JSOJVSBOEOWZJX-UHFFFAOYSA-N [O].N1=CC=CC2=CC=CC=C21 Chemical compound [O].N1=CC=CC2=CC=CC=C21 JSOJVSBOEOWZJX-UHFFFAOYSA-N 0.000 claims description 3
- 150000001336 alkenes Chemical class 0.000 claims description 3
- 239000004411 aluminium Substances 0.000 claims description 3
- 229910052782 aluminium Inorganic materials 0.000 claims description 3
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 3
- JLHMVTORNNQCRM-UHFFFAOYSA-N ethylphosphine Chemical compound CCP JLHMVTORNNQCRM-UHFFFAOYSA-N 0.000 claims description 3
- JFSPBVWPKOEZCB-UHFFFAOYSA-N fenfuram Chemical compound O1C=CC(C(=O)NC=2C=CC=CC=2)=C1C JFSPBVWPKOEZCB-UHFFFAOYSA-N 0.000 claims description 3
- IQECZGDVZMVJSH-UHFFFAOYSA-N furan 1H-pyrazole Chemical class O1C=CC=C1.N1N=CC=C1 IQECZGDVZMVJSH-UHFFFAOYSA-N 0.000 claims description 3
- 229910052736 halogen Inorganic materials 0.000 claims description 3
- 150000002367 halogens Chemical class 0.000 claims description 3
- 229940017219 methyl propionate Drugs 0.000 claims description 3
- WUHLVXDDBHWHLQ-UHFFFAOYSA-N pentazole Chemical class N=1N=NNN=1 WUHLVXDDBHWHLQ-UHFFFAOYSA-N 0.000 claims description 3
- YEBIHIICWDDQOL-YBHNRIQQSA-N polyoxin Polymers O[C@@H]1[C@H](O)[C@@H](C(C=O)N)O[C@H]1N1C(=O)NC(=O)C(C(O)=O)=C1 YEBIHIICWDDQOL-YBHNRIQQSA-N 0.000 claims description 3
- 235000015096 spirit Nutrition 0.000 claims description 3
- 229910052717 sulfur Inorganic materials 0.000 claims description 3
- 150000004867 thiadiazoles Chemical class 0.000 claims description 3
- FFSJPOPLSWBGQY-UHFFFAOYSA-N triazol-4-one Chemical compound O=C1C=NN=N1 FFSJPOPLSWBGQY-UHFFFAOYSA-N 0.000 claims description 3
- AMHNZOICSMBGDH-UHFFFAOYSA-L zineb Chemical compound [Zn+2].[S-]C(=S)NCCNC([S-])=S AMHNZOICSMBGDH-UHFFFAOYSA-L 0.000 claims description 3
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 claims description 2
- RHVBNSKOADZUJF-UHFFFAOYSA-N 1,2,4-triazole-1-sulfonamide Chemical compound NS(=O)(=O)N1C=NC=N1 RHVBNSKOADZUJF-UHFFFAOYSA-N 0.000 claims description 2
- NSPMIYGKQJPBQR-UHFFFAOYSA-N 4H-1,2,4-triazole Chemical class C=1N=CNN=1 NSPMIYGKQJPBQR-UHFFFAOYSA-N 0.000 claims description 2
- 230000003115 biocidal effect Effects 0.000 claims description 2
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 2
- RXDMAYSSBPYBFW-PKFCDNJMSA-N carpropamide Chemical compound N([C@@H](C)C=1C=CC(Cl)=CC=1)C(=O)[C@@]1(CC)[C@H](C)C1(Cl)Cl RXDMAYSSBPYBFW-PKFCDNJMSA-N 0.000 claims description 2
- AEJIMXVJZFYIHN-UHFFFAOYSA-N copper;dihydrate Chemical compound O.O.[Cu] AEJIMXVJZFYIHN-UHFFFAOYSA-N 0.000 claims description 2
- 150000002357 guanidines Chemical class 0.000 claims description 2
- 150000002391 heterocyclic compounds Chemical class 0.000 claims description 2
- 150000002431 hydrogen Chemical class 0.000 claims description 2
- 150000002902 organometallic compounds Chemical class 0.000 claims description 2
- 239000011593 sulfur Substances 0.000 claims description 2
- ISIJQEHRDSCQIU-UHFFFAOYSA-N tert-butyl 2,7-diazaspiro[4.5]decane-7-carboxylate Chemical compound C1N(C(=O)OC(C)(C)C)CCCC11CNCC1 ISIJQEHRDSCQIU-UHFFFAOYSA-N 0.000 claims description 2
- LITQZINTSYBKIU-UHFFFAOYSA-F tetracopper;hexahydroxide;sulfate Chemical compound [OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[Cu+2].[Cu+2].[Cu+2].[Cu+2].[O-]S([O-])(=O)=O LITQZINTSYBKIU-UHFFFAOYSA-F 0.000 claims description 2
- SBXWFLISHPUINY-UHFFFAOYSA-N triphenyltin Chemical class C1=CC=CC=C1[Sn](C=1C=CC=CC=1)C1=CC=CC=C1 SBXWFLISHPUINY-UHFFFAOYSA-N 0.000 claims description 2
- HTSGKJQDMSTCGS-UHFFFAOYSA-N 1,4-bis(4-chlorophenyl)-2-(4-methylphenyl)sulfonylbutane-1,4-dione Chemical compound C1=CC(C)=CC=C1S(=O)(=O)C(C(=O)C=1C=CC(Cl)=CC=1)CC(=O)C1=CC=C(Cl)C=C1 HTSGKJQDMSTCGS-UHFFFAOYSA-N 0.000 claims 1
- 230000002538 fungal effect Effects 0.000 claims 1
- 239000007788 liquid Substances 0.000 claims 1
- 239000013543 active substance Substances 0.000 abstract description 7
- 239000003795 chemical substances by application Substances 0.000 abstract description 3
- BBXXLROWFHWFQY-UHFFFAOYSA-N ethirimol Chemical compound CCCCC1=C(C)NC(NCC)=NC1=O BBXXLROWFHWFQY-UHFFFAOYSA-N 0.000 abstract description 2
- ZRALSGWEFCBTJO-UHFFFAOYSA-N Guanidine Chemical compound NC(N)=N ZRALSGWEFCBTJO-UHFFFAOYSA-N 0.000 abstract 2
- VSNHCAURESNICA-UHFFFAOYSA-N Hydroxyurea Chemical compound NC(=O)NO VSNHCAURESNICA-UHFFFAOYSA-N 0.000 abstract 1
- CHJJGSNFBQVOTG-UHFFFAOYSA-N N-methyl-guanidine Natural products CNC(N)=N CHJJGSNFBQVOTG-UHFFFAOYSA-N 0.000 abstract 1
- GRTOGORTSDXSFK-XJTZBENFSA-N ajmalicine Chemical compound C1=CC=C2C(CCN3C[C@@H]4[C@H](C)OC=C([C@H]4C[C@H]33)C(=O)OC)=C3NC2=C1 GRTOGORTSDXSFK-XJTZBENFSA-N 0.000 abstract 1
- 239000003242 anti bacterial agent Substances 0.000 abstract 1
- 229940088710 antibiotic agent Drugs 0.000 abstract 1
- 229940058344 antitrematodals organophosphorous compound Drugs 0.000 abstract 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 abstract 1
- SWSQBOPZIKWTGO-UHFFFAOYSA-N dimethylaminoamidine Natural products CN(C)C(N)=N SWSQBOPZIKWTGO-UHFFFAOYSA-N 0.000 abstract 1
- 125000000623 heterocyclic group Chemical group 0.000 abstract 1
- 239000002585 base Substances 0.000 description 41
- 230000000694 effects Effects 0.000 description 26
- 241000196324 Embryophyta Species 0.000 description 23
- DRSHXJFUUPIBHX-UHFFFAOYSA-N COc1ccc(cc1)N1N=CC2C=NC(Nc3cc(OC)c(OC)c(OCCCN4CCN(C)CC4)c3)=NC12 Chemical compound COc1ccc(cc1)N1N=CC2C=NC(Nc3cc(OC)c(OC)c(OCCCN4CCN(C)CC4)c3)=NC12 DRSHXJFUUPIBHX-UHFFFAOYSA-N 0.000 description 20
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 20
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 13
- 239000000839 emulsion Substances 0.000 description 12
- 239000000725 suspension Substances 0.000 description 12
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 10
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 9
- 239000002270 dispersing agent Substances 0.000 description 9
- 239000003995 emulsifying agent Substances 0.000 description 8
- 239000000843 powder Substances 0.000 description 8
- 239000000047 product Substances 0.000 description 8
- 239000000243 solution Substances 0.000 description 8
- 239000000080 wetting agent Substances 0.000 description 8
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 7
- 241000123650 Botrytis cinerea Species 0.000 description 7
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 7
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 7
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 7
- 229910052794 bromium Inorganic materials 0.000 description 7
- 238000010790 dilution Methods 0.000 description 7
- 239000012895 dilution Substances 0.000 description 7
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 7
- 239000011630 iodine Substances 0.000 description 7
- 229910052740 iodine Inorganic materials 0.000 description 7
- 239000002245 particle Substances 0.000 description 7
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 7
- 239000002904 solvent Substances 0.000 description 7
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 7
- DLFVBJFMPXGRIB-UHFFFAOYSA-N Acetamide Chemical compound CC(N)=O DLFVBJFMPXGRIB-UHFFFAOYSA-N 0.000 description 6
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 6
- 240000007594 Oryza sativa Species 0.000 description 6
- 240000006365 Vitis vinifera Species 0.000 description 6
- 235000014787 Vitis vinifera Nutrition 0.000 description 6
- 235000013339 cereals Nutrition 0.000 description 6
- 239000012141 concentrate Substances 0.000 description 6
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 6
- ZHNUHDYFZUAESO-UHFFFAOYSA-N formamide Substances NC=O ZHNUHDYFZUAESO-UHFFFAOYSA-N 0.000 description 6
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 6
- 239000011550 stock solution Substances 0.000 description 6
- 235000007164 Oryza sativa Nutrition 0.000 description 5
- 241000209140 Triticum Species 0.000 description 5
- 235000021307 Triticum Nutrition 0.000 description 5
- 239000006185 dispersion Substances 0.000 description 5
- 238000010410 dusting Methods 0.000 description 5
- 239000006072 paste Substances 0.000 description 5
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 5
- 235000009566 rice Nutrition 0.000 description 5
- 241000221785 Erysiphales Species 0.000 description 4
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N N-phenyl amine Natural products NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 4
- 241000233622 Phytophthora infestans Species 0.000 description 4
- 239000007859 condensation product Substances 0.000 description 4
- 235000014113 dietary fatty acids Nutrition 0.000 description 4
- 239000000194 fatty acid Substances 0.000 description 4
- 229930195729 fatty acid Natural products 0.000 description 4
- 238000000227 grinding Methods 0.000 description 4
- 238000011081 inoculation Methods 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- GTCAXTIRRLKXRU-UHFFFAOYSA-N methyl carbamate Chemical compound COC(N)=O GTCAXTIRRLKXRU-UHFFFAOYSA-N 0.000 description 4
- 239000004533 oil dispersion Substances 0.000 description 4
- 229920000151 polyglycol Polymers 0.000 description 4
- 239000010695 polyglycol Substances 0.000 description 4
- 239000003643 water by type Substances 0.000 description 4
- YABFPHSQTSFWQB-UHFFFAOYSA-N 2-(4-fluorophenyl)-1-(1,2,4-triazol-1-yl)-3-(trimethylsilyl)propan-2-ol Chemical compound C=1C=C(F)C=CC=1C(O)(C[Si](C)(C)C)CN1C=NC=N1 YABFPHSQTSFWQB-UHFFFAOYSA-N 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
- 239000005995 Aluminium silicate Substances 0.000 description 3
- WVDDGKGOMKODPV-UHFFFAOYSA-N Benzyl alcohol Chemical compound OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 description 3
- 206010017533 Fungal infection Diseases 0.000 description 3
- 208000031888 Mycoses Diseases 0.000 description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Natural products NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 3
- 235000012211 aluminium silicate Nutrition 0.000 description 3
- 239000004359 castor oil Substances 0.000 description 3
- 235000019438 castor oil Nutrition 0.000 description 3
- 239000004927 clay Substances 0.000 description 3
- 150000004665 fatty acids Chemical class 0.000 description 3
- 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 3
- 239000004009 herbicide Substances 0.000 description 3
- 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 3
- 150000002790 naphthalenes Chemical class 0.000 description 3
- 239000003921 oil Substances 0.000 description 3
- 239000003960 organic solvent Substances 0.000 description 3
- 238000009331 sowing Methods 0.000 description 3
- 239000007921 spray Substances 0.000 description 3
- HIIRDDUVRXCDBN-SDXDJHTJSA-N (2z)-2-methoxyimino-n-methyl-2-(2-phenoxyphenyl)acetamide Chemical compound CNC(=O)C(=N/OC)\C1=CC=CC=C1OC1=CC=CC=C1 HIIRDDUVRXCDBN-SDXDJHTJSA-N 0.000 description 2
- DNIAPMSPPWPWGF-GSVOUGTGSA-N (R)-(-)-Propylene glycol Chemical compound C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-N 0.000 description 2
- WURBVZBTWMNKQT-UHFFFAOYSA-N 1-(4-chlorophenoxy)-3,3-dimethyl-1-(1,2,4-triazol-1-yl)butan-2-one Chemical compound C1=NC=NN1C(C(=O)C(C)(C)C)OC1=CC=C(Cl)C=C1 WURBVZBTWMNKQT-UHFFFAOYSA-N 0.000 description 2
- HYZJCKYKOHLVJF-UHFFFAOYSA-N 1H-benzimidazole Chemical compound C1=CC=C2NC=NC2=C1 HYZJCKYKOHLVJF-UHFFFAOYSA-N 0.000 description 2
- STMIIPIFODONDC-UHFFFAOYSA-N 2-(2,4-dichlorophenyl)-1-(1H-1,2,4-triazol-1-yl)hexan-2-ol Chemical compound C=1C=C(Cl)C=C(Cl)C=1C(O)(CCCC)CN1C=NC=N1 STMIIPIFODONDC-UHFFFAOYSA-N 0.000 description 2
- HZJKXKUJVSEEFU-UHFFFAOYSA-N 2-(4-chlorophenyl)-2-(1H-1,2,4-triazol-1-ylmethyl)hexanenitrile Chemical compound C=1C=C(Cl)C=CC=1C(CCCC)(C#N)CN1C=NC=N1 HZJKXKUJVSEEFU-UHFFFAOYSA-N 0.000 description 2
- KWLVWJPJKJMCSH-UHFFFAOYSA-N 2-(4-chlorophenyl)-N-{2-[3-methoxy-4-(prop-2-yn-1-yloxy)phenyl]ethyl}-2-(prop-2-yn-1-yloxy)acetamide Chemical compound C1=C(OCC#C)C(OC)=CC(CCNC(=O)C(OCC#C)C=2C=CC(Cl)=CC=2)=C1 KWLVWJPJKJMCSH-UHFFFAOYSA-N 0.000 description 2
- WNZQDUSMALZDQF-UHFFFAOYSA-N 2-benzofuran-1(3H)-one Chemical compound C1=CC=C2C(=O)OCC2=C1 WNZQDUSMALZDQF-UHFFFAOYSA-N 0.000 description 2
- OWDLFBLNMPCXSD-UHFFFAOYSA-N 2-chloro-N-(2,6-dimethylphenyl)-N-(2-oxotetrahydrofuran-3-yl)acetamide Chemical compound CC1=CC=CC(C)=C1N(C(=O)CCl)C1C(=O)OCC1 OWDLFBLNMPCXSD-UHFFFAOYSA-N 0.000 description 2
- XXUNIGZDNWWYED-UHFFFAOYSA-N 2-methylbenzamide Chemical compound CC1=CC=CC=C1C(N)=O XXUNIGZDNWWYED-UHFFFAOYSA-N 0.000 description 2
- ZRNSSRODJSSVEJ-UHFFFAOYSA-N 2-methylpentacosane Chemical compound CCCCCCCCCCCCCCCCCCCCCCCC(C)C ZRNSSRODJSSVEJ-UHFFFAOYSA-N 0.000 description 2
- UHPMCKVQTMMPCG-UHFFFAOYSA-N 5,8-dihydroxy-2-methoxy-6-methyl-7-(2-oxopropyl)naphthalene-1,4-dione Chemical compound CC1=C(CC(C)=O)C(O)=C2C(=O)C(OC)=CC(=O)C2=C1O UHPMCKVQTMMPCG-UHFFFAOYSA-N 0.000 description 2
- NRTLIYOWLVMQBO-UHFFFAOYSA-N 5-chloro-1,3-dimethyl-N-(1,1,3-trimethyl-1,3-dihydro-2-benzofuran-4-yl)pyrazole-4-carboxamide Chemical compound C=12C(C)OC(C)(C)C2=CC=CC=1NC(=O)C=1C(C)=NN(C)C=1Cl NRTLIYOWLVMQBO-UHFFFAOYSA-N 0.000 description 2
- PMZBHPUNQNKBOA-UHFFFAOYSA-N 5-methylbenzene-1,3-dicarboxylic acid Chemical compound CC1=CC(C(O)=O)=CC(C(O)=O)=C1 PMZBHPUNQNKBOA-UHFFFAOYSA-N 0.000 description 2
- 235000001674 Agaricus brunnescens Nutrition 0.000 description 2
- 241000235349 Ascomycota Species 0.000 description 2
- 241000221198 Basidiomycota Species 0.000 description 2
- KXDAEFPNCMNJSK-UHFFFAOYSA-N Benzamide Chemical compound NC(=O)C1=CC=CC=C1 KXDAEFPNCMNJSK-UHFFFAOYSA-N 0.000 description 2
- 235000008534 Capsicum annuum var annuum Nutrition 0.000 description 2
- 240000008384 Capsicum annuum var. annuum Species 0.000 description 2
- 229940126062 Compound A Drugs 0.000 description 2
- 229920000742 Cotton Polymers 0.000 description 2
- XPDWGBQVDMORPB-UHFFFAOYSA-N Fluoroform Chemical compound FC(F)F XPDWGBQVDMORPB-UHFFFAOYSA-N 0.000 description 2
- 241000223218 Fusarium Species 0.000 description 2
- NLDMNSXOCDLTTB-UHFFFAOYSA-N Heterophylliin A Natural products O1C2COC(=O)C3=CC(O)=C(O)C(O)=C3C3=C(O)C(O)=C(O)C=C3C(=O)OC2C(OC(=O)C=2C=C(O)C(O)=C(O)C=2)C(O)C1OC(=O)C1=CC(O)=C(O)C(O)=C1 NLDMNSXOCDLTTB-UHFFFAOYSA-N 0.000 description 2
- 241000238631 Hexapoda Species 0.000 description 2
- 240000005979 Hordeum vulgare Species 0.000 description 2
- 235000007340 Hordeum vulgare Nutrition 0.000 description 2
- 235000007688 Lycopersicon esculentum Nutrition 0.000 description 2
- 241001330975 Magnaporthe oryzae Species 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
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 2
- 240000005561 Musa balbisiana Species 0.000 description 2
- 235000018290 Musa x paradisiaca Nutrition 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical class CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 2
- 241000233654 Oomycetes Species 0.000 description 2
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 2
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 2
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 2
- 241000540505 Puccinia dispersa f. sp. tritici Species 0.000 description 2
- 241001361634 Rhizoctonia Species 0.000 description 2
- 240000000111 Saccharum officinarum Species 0.000 description 2
- 235000007201 Saccharum officinarum Nutrition 0.000 description 2
- 240000003768 Solanum lycopersicum Species 0.000 description 2
- 244000061456 Solanum tuberosum Species 0.000 description 2
- 235000002595 Solanum tuberosum Nutrition 0.000 description 2
- LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical compound OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 description 2
- 235000009754 Vitis X bourquina Nutrition 0.000 description 2
- 235000012333 Vitis X labruscana Nutrition 0.000 description 2
- KXKVLQRXCPHEJC-UHFFFAOYSA-N acetic acid trimethyl ester Natural products COC(C)=O KXKVLQRXCPHEJC-UHFFFAOYSA-N 0.000 description 2
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 description 2
- 239000008186 active pharmaceutical agent Substances 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 230000000996 additive effect Effects 0.000 description 2
- 239000002671 adjuvant Substances 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- 150000008052 alkyl sulfonates Chemical class 0.000 description 2
- 230000008485 antagonism Effects 0.000 description 2
- 230000000843 anti-fungal effect Effects 0.000 description 2
- 229940121375 antifungal agent Drugs 0.000 description 2
- 239000012752 auxiliary agent Substances 0.000 description 2
- VVSLYIKSEBPRSN-PELKAZGASA-N benthiavalicarb Chemical compound C1=C(F)C=C2SC([C@@H](C)NC(=O)[C@@H](NC(O)=O)C(C)C)=NC2=C1 VVSLYIKSEBPRSN-PELKAZGASA-N 0.000 description 2
- IOJUPLGTWVMSFF-UHFFFAOYSA-N benzothiazole Chemical compound C1=CC=C2SC=NC2=C1 IOJUPLGTWVMSFF-UHFFFAOYSA-N 0.000 description 2
- 229940073608 benzyl chloride Drugs 0.000 description 2
- 230000008033 biological extinction Effects 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
- OOCMUZJPDXYRFD-UHFFFAOYSA-L calcium;2-dodecylbenzenesulfonate Chemical compound [Ca+2].CCCCCCCCCCCCC1=CC=CC=C1S([O-])(=O)=O.CCCCCCCCCCCCC1=CC=CC=C1S([O-])(=O)=O OOCMUZJPDXYRFD-UHFFFAOYSA-L 0.000 description 2
- 239000004202 carbamide Substances 0.000 description 2
- 235000013877 carbamide Nutrition 0.000 description 2
- VBJZWFWINSGBLK-UHFFFAOYSA-N carbamodithioic acid;ethene;zinc Chemical compound [Zn].C=C.NC(S)=S VBJZWFWINSGBLK-UHFFFAOYSA-N 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- RXDMAYSSBPYBFW-UHFFFAOYSA-N carpropamid Chemical compound C=1C=C(Cl)C=CC=1C(C)NC(=O)C1(CC)C(C)C1(Cl)Cl RXDMAYSSBPYBFW-UHFFFAOYSA-N 0.000 description 2
- YXKMMRDKEKCERS-UHFFFAOYSA-N cyazofamid Chemical compound CN(C)S(=O)(=O)N1C(C#N)=NC(Cl)=C1C1=CC=C(C)C=C1 YXKMMRDKEKCERS-UHFFFAOYSA-N 0.000 description 2
- MZGNSEAPZQGJRB-UHFFFAOYSA-M dimethyldithiocarbamate Chemical compound CN(C)C([S-])=S MZGNSEAPZQGJRB-UHFFFAOYSA-M 0.000 description 2
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical group C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 235000013399 edible fruits Nutrition 0.000 description 2
- 238000007046 ethoxylation reaction Methods 0.000 description 2
- IGUYEXXAGBDLLX-UHFFFAOYSA-N ethyl 3-(3,5-dichlorophenyl)-5-methyl-2,4-dioxo-1,3-oxazolidine-5-carboxylate Chemical compound O=C1C(C(=O)OCC)(C)OC(=O)N1C1=CC(Cl)=CC(Cl)=C1 IGUYEXXAGBDLLX-UHFFFAOYSA-N 0.000 description 2
- 150000002191 fatty alcohols Chemical class 0.000 description 2
- 239000003337 fertilizer Substances 0.000 description 2
- 125000003784 fluoroethyl group Chemical group [H]C([H])(F)C([H])([H])* 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- 239000000499 gel Substances 0.000 description 2
- LELOWRISYMNNSU-UHFFFAOYSA-N hydrogen cyanide Chemical compound N#C LELOWRISYMNNSU-UHFFFAOYSA-N 0.000 description 2
- 229910052500 inorganic mineral Inorganic materials 0.000 description 2
- QTYCMDBMOLSEAM-UHFFFAOYSA-N ipconazole Chemical compound C1=NC=NN1CC1(O)C(C(C)C)CCC1CC1=CC=C(Cl)C=C1 QTYCMDBMOLSEAM-UHFFFAOYSA-N 0.000 description 2
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 2
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 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
- HYVVJDQGXFXBRZ-UHFFFAOYSA-N metam Chemical compound CNC(S)=S HYVVJDQGXFXBRZ-UHFFFAOYSA-N 0.000 description 2
- 229920000609 methyl cellulose Polymers 0.000 description 2
- 239000001923 methylcellulose Substances 0.000 description 2
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 description 2
- 239000011707 mineral Substances 0.000 description 2
- 235000010755 mineral Nutrition 0.000 description 2
- 239000002480 mineral oil Substances 0.000 description 2
- 235000010446 mineral oil Nutrition 0.000 description 2
- NBVXSUQYWXRMNV-UHFFFAOYSA-N monofluoromethane Natural products FC NBVXSUQYWXRMNV-UHFFFAOYSA-N 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
- 238000010899 nucleation Methods 0.000 description 2
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- 239000012188 paraffin wax Substances 0.000 description 2
- 239000000575 pesticide Substances 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 2
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 2
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 2
- QLNJFJADRCOGBJ-UHFFFAOYSA-N propionamide Chemical compound CCC(N)=O QLNJFJADRCOGBJ-UHFFFAOYSA-N 0.000 description 2
- 229940080818 propionamide Drugs 0.000 description 2
- 239000000741 silica gel Substances 0.000 description 2
- 229910002027 silica gel Inorganic materials 0.000 description 2
- 239000004550 soluble concentrate Substances 0.000 description 2
- 238000005507 spraying Methods 0.000 description 2
- 229940124530 sulfonamide Drugs 0.000 description 2
- 239000004094 surface-active agent Substances 0.000 description 2
- 239000000454 talc Substances 0.000 description 2
- 235000012222 talc Nutrition 0.000 description 2
- 229910052623 talc Inorganic materials 0.000 description 2
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 2
- KUAZQDVKQLNFPE-UHFFFAOYSA-N thiram Chemical compound CN(C)C(=S)SSC(=S)N(C)C KUAZQDVKQLNFPE-UHFFFAOYSA-N 0.000 description 2
- LDHQCZJRKDOVOX-UHFFFAOYSA-N trans-crotonic acid Natural products CC=CC(O)=O LDHQCZJRKDOVOX-UHFFFAOYSA-N 0.000 description 2
- 125000003866 trichloromethyl group Chemical group ClC(Cl)(Cl)* 0.000 description 2
- 235000013311 vegetables Nutrition 0.000 description 2
- 229920002554 vinyl polymer Polymers 0.000 description 2
- 239000002699 waste material Substances 0.000 description 2
- 239000004552 water soluble powder 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
- ZMYFCFLJBGAQRS-IRXDYDNUSA-N (2R,3S)-epoxiconazole Chemical compound C1=CC(F)=CC=C1[C@@]1(CN2N=CN=C2)[C@H](C=2C(=CC=CC=2)Cl)O1 ZMYFCFLJBGAQRS-IRXDYDNUSA-N 0.000 description 1
- RYAUSSKQMZRMAI-ALOPSCKCSA-N (2S,6R)-4-[3-(4-tert-butylphenyl)-2-methylpropyl]-2,6-dimethylmorpholine Chemical compound C=1C=C(C(C)(C)C)C=CC=1CC(C)CN1C[C@H](C)O[C@H](C)C1 RYAUSSKQMZRMAI-ALOPSCKCSA-N 0.000 description 1
- WVHAIMKMNMGHMX-UHFFFAOYSA-N (4-fluorophenyl)-methylsilane Chemical compound FC1=CC=C(C=C1)[SiH2]C WVHAIMKMNMGHMX-UHFFFAOYSA-N 0.000 description 1
- 125000002030 1,2-phenylene group Chemical group [H]C1=C([H])C([*:1])=C([*:2])C([H])=C1[H] 0.000 description 1
- ZPQOPVIELGIULI-UHFFFAOYSA-N 1,3-dichlorobenzene Chemical compound ClC1=CC=CC(Cl)=C1 ZPQOPVIELGIULI-UHFFFAOYSA-N 0.000 description 1
- LQDARGUHUSPFNL-UHFFFAOYSA-N 1-[2-(2,4-dichlorophenyl)-3-(1,1,2,2-tetrafluoroethoxy)propyl]1,2,4-triazole Chemical compound C=1C=C(Cl)C=C(Cl)C=1C(COC(F)(F)C(F)F)CN1C=NC=N1 LQDARGUHUSPFNL-UHFFFAOYSA-N 0.000 description 1
- 125000006083 1-bromoethyl group Chemical group 0.000 description 1
- 125000001478 1-chloroethyl group Chemical group [H]C([H])([H])C([H])(Cl)* 0.000 description 1
- 125000004776 1-fluoroethyl group Chemical group [H]C([H])([H])C([H])(F)* 0.000 description 1
- PFFIDZXUXFLSSR-UHFFFAOYSA-N 1-methyl-N-[2-(4-methylpentan-2-yl)-3-thienyl]-3-(trifluoromethyl)pyrazole-4-carboxamide Chemical compound S1C=CC(NC(=O)C=2C(=NN(C)C=2)C(F)(F)F)=C1C(C)CC(C)C PFFIDZXUXFLSSR-UHFFFAOYSA-N 0.000 description 1
- 125000004206 2,2,2-trifluoroethyl group Chemical group [H]C([H])(*)C(F)(F)F 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
- NJUVWIKMOXUXSS-UHFFFAOYSA-N 2-(4-chlorophenyl)-3-methyl-2-(1,2,4-triazol-1-yl)pentanenitrile Chemical compound C1=NC=NN1C(C#N)(C(C)CC)C1=CC=C(Cl)C=C1 NJUVWIKMOXUXSS-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
- HLSLWZHVCLXIMI-UHFFFAOYSA-N 2-(triazol-1-yl)-1h-quinazolin-4-one Chemical compound N1C2=CC=CC=C2C(=O)N=C1N1C=CN=N1 HLSLWZHVCLXIMI-UHFFFAOYSA-N 0.000 description 1
- MNHVNIJQQRJYDH-UHFFFAOYSA-N 2-[2-(1-chlorocyclopropyl)-3-(2-chlorophenyl)-2-hydroxypropyl]-1,2-dihydro-1,2,4-triazole-3-thione Chemical compound N1=CNC(=S)N1CC(C1(Cl)CC1)(O)CC1=CC=CC=C1Cl MNHVNIJQQRJYDH-UHFFFAOYSA-N 0.000 description 1
- JTXMVXSTHSMVQF-UHFFFAOYSA-N 2-acetyloxyethyl acetate Chemical compound CC(=O)OCCOC(C)=O JTXMVXSTHSMVQF-UHFFFAOYSA-N 0.000 description 1
- 125000004779 2-chloro-2-fluoroethyl group Chemical group [H]C([H])(*)C([H])(F)Cl 0.000 description 1
- ONKIWRZLPZCYDL-UHFFFAOYSA-N 2-chloro-4-(4-fluorophenoxy)quinoline Chemical compound C1=CC(F)=CC=C1OC1=CC(Cl)=NC2=CC=CC=C12 ONKIWRZLPZCYDL-UHFFFAOYSA-N 0.000 description 1
- 125000004777 2-fluoroethyl group Chemical group [H]C([H])(F)C([H])([H])* 0.000 description 1
- 229940044120 2-n-octyl-4-isothiazolin-3-one Drugs 0.000 description 1
- AVGVFDSUDIUXEU-UHFFFAOYSA-N 2-octyl-1,2-thiazolidin-3-one Chemical compound CCCCCCCCN1SCCC1=O AVGVFDSUDIUXEU-UHFFFAOYSA-N 0.000 description 1
- DUIOKRXOKLLURE-UHFFFAOYSA-N 2-octylphenol Chemical compound CCCCCCCCC1=CC=CC=C1O DUIOKRXOKLLURE-UHFFFAOYSA-N 0.000 description 1
- 125000000094 2-phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])* 0.000 description 1
- PFTZLFKMQOYCLG-UHFFFAOYSA-N 3,5-dimethyl-1,3,5-thiadiazinane Chemical compound CN1CSCN(C)C1 PFTZLFKMQOYCLG-UHFFFAOYSA-N 0.000 description 1
- YEJRWHAVMIAJKC-UHFFFAOYSA-N 4-Butyrolactone Chemical compound O=C1CCCO1 YEJRWHAVMIAJKC-UHFFFAOYSA-N 0.000 description 1
- SBUKOHLFHYSZNG-UHFFFAOYSA-N 4-dodecyl-2,6-dimethylmorpholine Chemical compound CCCCCCCCCCCCN1CC(C)OC(C)C1 SBUKOHLFHYSZNG-UHFFFAOYSA-N 0.000 description 1
- PPDBOQMNKNNODG-UHFFFAOYSA-N 5-[(4-chlorophenyl)methylidene]-2,2-dimethyl-1-(1,2,4-triazol-1-ylmethyl)cyclopentan-1-ol Chemical compound C1=NC=NN1CC1(O)C(C)(C)CCC1=CC1=CC=C(Cl)C=C1 PPDBOQMNKNNODG-UHFFFAOYSA-N 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- 239000005964 Acibenzolar-S-methyl Substances 0.000 description 1
- 241000223600 Alternaria Species 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical group N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 1
- 239000004254 Ammonium phosphate Substances 0.000 description 1
- 235000017060 Arachis glabrata Nutrition 0.000 description 1
- 244000105624 Arachis hypogaea Species 0.000 description 1
- 235000010777 Arachis hypogaea Nutrition 0.000 description 1
- 235000018262 Arachis monticola Nutrition 0.000 description 1
- 241000239290 Araneae Species 0.000 description 1
- 235000007319 Avena orientalis Nutrition 0.000 description 1
- 241000209763 Avena sativa Species 0.000 description 1
- 235000007558 Avena sp Nutrition 0.000 description 1
- 239000005730 Azoxystrobin Substances 0.000 description 1
- 239000005734 Benalaxyl Substances 0.000 description 1
- 239000005736 Benthiavalicarb Substances 0.000 description 1
- 241001465178 Bipolaris Species 0.000 description 1
- 241001480061 Blumeria graminis Species 0.000 description 1
- 241001465180 Botrytis Species 0.000 description 1
- 239000005742 Bupirimate Substances 0.000 description 1
- FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Natural products CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 description 1
- XKVXGAYDPAZBCM-UHFFFAOYSA-N CC1=C(C(=O)O)CCC=C1C(=O)O Chemical compound CC1=C(C(=O)O)CCC=C1C(=O)O XKVXGAYDPAZBCM-UHFFFAOYSA-N 0.000 description 1
- 239000005747 Chlorothalonil Substances 0.000 description 1
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 1
- 240000007154 Coffea arabica Species 0.000 description 1
- 240000008067 Cucumis sativus Species 0.000 description 1
- 235000010799 Cucumis sativus var sativus Nutrition 0.000 description 1
- 239000005754 Cyazofamid Substances 0.000 description 1
- 239000005758 Cyprodinil Substances 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
- WQZGKKKJIJFFOK-IVMDWMLBSA-N D-allopyranose Chemical compound OC[C@H]1OC(O)[C@H](O)[C@H](O)[C@@H]1O WQZGKKKJIJFFOK-IVMDWMLBSA-N 0.000 description 1
- 239000005759 Diethofencarb Substances 0.000 description 1
- 239000005760 Difenoconazole Substances 0.000 description 1
- 239000005762 Dimoxystrobin Substances 0.000 description 1
- 239000005764 Dithianon Substances 0.000 description 1
- 239000005765 Dodemorph Substances 0.000 description 1
- 239000005767 Epoxiconazole Substances 0.000 description 1
- 241000510928 Erysiphe necator Species 0.000 description 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
- 239000005769 Etridiazole Substances 0.000 description 1
- 239000005775 Fenbuconazole Substances 0.000 description 1
- 239000005778 Fenpropimorph Substances 0.000 description 1
- 239000005781 Fludioxonil Substances 0.000 description 1
- 235000016623 Fragaria vesca Nutrition 0.000 description 1
- 240000009088 Fragaria x ananassa Species 0.000 description 1
- 235000011363 Fragaria x ananassa Nutrition 0.000 description 1
- 239000005791 Fuberidazole Substances 0.000 description 1
- 244000068988 Glycine max Species 0.000 description 1
- 235000010469 Glycine max Nutrition 0.000 description 1
- 241000896246 Golovinomyces cichoracearum Species 0.000 description 1
- JBOPQACSHPPKEP-UHFFFAOYSA-N Indoxyl acetate Chemical compound C1=CC=C2C(OC(=O)C)=CNC2=C1 JBOPQACSHPPKEP-UHFFFAOYSA-N 0.000 description 1
- 239000005796 Ipconazole Substances 0.000 description 1
- 239000005867 Iprodione Substances 0.000 description 1
- 239000005800 Kresoxim-methyl Substances 0.000 description 1
- 235000019738 Limestone Nutrition 0.000 description 1
- LTGPFZWZZNUIIK-LURJTMIESA-N Lysol Chemical compound NCCCC[C@H](N)CO LTGPFZWZZNUIIK-LURJTMIESA-N 0.000 description 1
- 239000002169 Metam Substances 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- 239000005868 Metconazole Substances 0.000 description 1
- 239000005809 Metiram Substances 0.000 description 1
- 239000005811 Myclobutanil Substances 0.000 description 1
- 241000131448 Mycosphaerella Species 0.000 description 1
- IUOKJNROJISWRO-UHFFFAOYSA-N N-(2-cyano-3-methylbutan-2-yl)-2-(2,4-dichlorophenoxy)propanamide Chemical compound CC(C)C(C)(C#N)NC(=O)C(C)OC1=CC=C(Cl)C=C1Cl IUOKJNROJISWRO-UHFFFAOYSA-N 0.000 description 1
- ZKUVPNREOOUZRF-UHFFFAOYSA-N N-(dimethylsulfamoyl)-N-phenylthiohydroxylamine Chemical compound SN(S(=O)(=O)N(C)C)C1=CC=CC=C1 ZKUVPNREOOUZRF-UHFFFAOYSA-N 0.000 description 1
- XFOXDUJCOHBXRC-UHFFFAOYSA-N N-Ethyl-N-methyl-4-(trifluoromethyl)-2-(3,4-dimethoxyphenyl)benzamide Chemical compound CCN(C)C(=O)C1=CC=C(C(F)(F)F)C=C1C1=CC=C(OC)C(OC)=C1 XFOXDUJCOHBXRC-UHFFFAOYSA-N 0.000 description 1
- AMQJEAYHLZJPGS-UHFFFAOYSA-N N-Pentanol Chemical compound CCCCCO AMQJEAYHLZJPGS-UHFFFAOYSA-N 0.000 description 1
- GXCLVBGFBYZDAG-UHFFFAOYSA-N N-[2-(1H-indol-3-yl)ethyl]-N-methylprop-2-en-1-amine Chemical compound CN(CCC1=CNC2=C1C=CC=C2)CC=C GXCLVBGFBYZDAG-UHFFFAOYSA-N 0.000 description 1
- NQRFDNJEBWAUBL-UHFFFAOYSA-N N-[cyano(2-thienyl)methyl]-4-ethyl-2-(ethylamino)-1,3-thiazole-5-carboxamide Chemical compound S1C(NCC)=NC(CC)=C1C(=O)NC(C#N)C1=CC=CS1 NQRFDNJEBWAUBL-UHFFFAOYSA-N 0.000 description 1
- QMJXKBRERYEDJJ-UHFFFAOYSA-N N1(N=NC=C1)C1C(CCC1)(O)C Chemical compound N1(N=NC=C1)C1C(CCC1)(O)C QMJXKBRERYEDJJ-UHFFFAOYSA-N 0.000 description 1
- 241000244206 Nematoda Species 0.000 description 1
- DFPAKSUCGFBDDF-UHFFFAOYSA-N Nicotinamide Chemical compound NC(=O)C1=CC=CN=C1 DFPAKSUCGFBDDF-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
- 241001668536 Oculimacula yallundae Species 0.000 description 1
- 239000005816 Penthiopyrad Substances 0.000 description 1
- 241000233679 Peronosporaceae Species 0.000 description 1
- 244000046052 Phaseolus vulgaris Species 0.000 description 1
- 235000010627 Phaseolus vulgaris Nutrition 0.000 description 1
- 239000005818 Picoxystrobin Substances 0.000 description 1
- 241001281803 Plasmopara viticola Species 0.000 description 1
- 241000317981 Podosphaera fuliginea Species 0.000 description 1
- 241001337928 Podosphaera leucotricha Species 0.000 description 1
- 239000004721 Polyphenylene oxide Substances 0.000 description 1
- 239000005821 Propamocarb Substances 0.000 description 1
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 description 1
- 239000005824 Proquinazid Substances 0.000 description 1
- 239000005825 Prothioconazole Substances 0.000 description 1
- 241001281802 Pseudoperonospora Species 0.000 description 1
- 241000221300 Puccinia Species 0.000 description 1
- 241001123569 Puccinia recondita Species 0.000 description 1
- 241000221535 Pucciniales Species 0.000 description 1
- 241000228453 Pyrenophora Species 0.000 description 1
- 241000209056 Secale Species 0.000 description 1
- 235000007238 Secale cereale Nutrition 0.000 description 1
- 241001533598 Septoria Species 0.000 description 1
- 241001674391 Sphaerulina musiva Species 0.000 description 1
- 239000005837 Spiroxamine Substances 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- 239000005840 Tetraconazole Substances 0.000 description 1
- 239000005843 Thiram Substances 0.000 description 1
- 235000011941 Tilia x europaea Nutrition 0.000 description 1
- 239000005845 Tolclofos-methyl Substances 0.000 description 1
- 239000005857 Trifloxystrobin Substances 0.000 description 1
- 239000005858 Triflumizole Substances 0.000 description 1
- 241000221566 Ustilago Species 0.000 description 1
- JARYYMUOCXVXNK-UHFFFAOYSA-N Validamycin A Natural products OC1C(O)C(OC2C(C(O)C(O)C(CO)O2)O)C(CO)CC1NC1C=C(CO)C(O)C(O)C1O JARYYMUOCXVXNK-UHFFFAOYSA-N 0.000 description 1
- 241000228452 Venturia inaequalis Species 0.000 description 1
- 241000082085 Verticillium <Phyllachorales> Species 0.000 description 1
- 240000008042 Zea mays Species 0.000 description 1
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 1
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 1
- ZKBNUNIVNISNDB-UHFFFAOYSA-N [Cl].FC Chemical compound [Cl].FC ZKBNUNIVNISNDB-UHFFFAOYSA-N 0.000 description 1
- VLLDIVKWDYJNLM-UHFFFAOYSA-N [Mn].C(N)(S)=S.C=C Chemical compound [Mn].C(N)(S)=S.C=C VLLDIVKWDYJNLM-UHFFFAOYSA-N 0.000 description 1
- CEDZFAONRDZJKJ-UHFFFAOYSA-N [O].ClC1=CC=CC(=C1)Cl Chemical compound [O].ClC1=CC=CC(=C1)Cl CEDZFAONRDZJKJ-UHFFFAOYSA-N 0.000 description 1
- DHKHKXVYLBGOIT-UHFFFAOYSA-N acetaldehyde Diethyl Acetal Natural products CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 description 1
- UELITFHSCLAHKR-UHFFFAOYSA-N acibenzolar-S-methyl Chemical group CSC(=O)C1=CC=CC2=C1SN=N2 UELITFHSCLAHKR-UHFFFAOYSA-N 0.000 description 1
- 239000011149 active material Substances 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001447 alkali salts Chemical class 0.000 description 1
- 125000002877 alkyl aryl group Chemical group 0.000 description 1
- 150000008055 alkyl aryl sulfonates Chemical class 0.000 description 1
- 150000005215 alkyl ethers Chemical class 0.000 description 1
- 125000005037 alkyl phenyl group Chemical group 0.000 description 1
- 150000008051 alkyl sulfates Chemical class 0.000 description 1
- 229910000329 aluminium sulfate Inorganic materials 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
- 150000001450 anions Chemical class 0.000 description 1
- 230000000844 anti-bacterial effect Effects 0.000 description 1
- 239000007900 aqueous suspension Substances 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- WFDXOXNFNRHQEC-GHRIWEEISA-N azoxystrobin Chemical compound CO\C=C(\C(=O)OC)C1=CC=CC=C1OC1=CC(OC=2C(=CC=CC=2)C#N)=NC=N1 WFDXOXNFNRHQEC-GHRIWEEISA-N 0.000 description 1
- 239000003899 bactericide agent Substances 0.000 description 1
- 125000005605 benzo group Chemical group 0.000 description 1
- 235000019445 benzyl alcohol Nutrition 0.000 description 1
- 229960004217 benzyl alcohol Drugs 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
- 239000004305 biphenyl Substances 0.000 description 1
- 235000010290 biphenyl Nutrition 0.000 description 1
- OIPMQULDKWSNGX-UHFFFAOYSA-N bis[[ethoxy(oxo)phosphaniumyl]oxy]alumanyloxy-ethoxy-oxophosphanium Chemical compound [Al+3].CCO[P+]([O-])=O.CCO[P+]([O-])=O.CCO[P+]([O-])=O OIPMQULDKWSNGX-UHFFFAOYSA-N 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 125000005997 bromomethyl group Chemical group 0.000 description 1
- DSKJPMWIHSOYEA-UHFFFAOYSA-N bupirimate Chemical compound CCCCC1=C(C)N=C(NCC)N=C1OS(=O)(=O)N(C)C DSKJPMWIHSOYEA-UHFFFAOYSA-N 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
- 235000011132 calcium sulphate Nutrition 0.000 description 1
- 239000001175 calcium sulphate Substances 0.000 description 1
- JHRWWRDRBPCWTF-OLQVQODUSA-N captafol Chemical compound C1C=CC[C@H]2C(=O)N(SC(Cl)(Cl)C(Cl)Cl)C(=O)[C@H]21 JHRWWRDRBPCWTF-OLQVQODUSA-N 0.000 description 1
- DKVNPHBNOWQYFE-UHFFFAOYSA-N carbamodithioic acid Chemical compound NC(S)=S DKVNPHBNOWQYFE-UHFFFAOYSA-N 0.000 description 1
- TXSULMYZLWFIAT-UHFFFAOYSA-N carbamodithioic acid;ethene Chemical compound C=C.NC(S)=S TXSULMYZLWFIAT-UHFFFAOYSA-N 0.000 description 1
- WCBCMSHWSDPDBE-UHFFFAOYSA-N carbamodithioic acid;zinc Chemical compound [Zn].NC(S)=S WCBCMSHWSDPDBE-UHFFFAOYSA-N 0.000 description 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 125000002603 chloroethyl group Chemical group [H]C([*])([H])C([H])([H])Cl 0.000 description 1
- 125000004218 chloromethyl group Chemical group [H]C([H])(Cl)* 0.000 description 1
- CRQQGFGUEAVUIL-UHFFFAOYSA-N chlorothalonil Chemical compound ClC1=C(Cl)C(C#N)=C(Cl)C(C#N)=C1Cl CRQQGFGUEAVUIL-UHFFFAOYSA-N 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
- 235000016213 coffee Nutrition 0.000 description 1
- 235000013353 coffee beverage Nutrition 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 235000005822 corn Nutrition 0.000 description 1
- 244000038559 crop plants Species 0.000 description 1
- LDHQCZJRKDOVOX-NSCUHMNNSA-N crotonic acid Chemical compound C\C=C\C(O)=O LDHQCZJRKDOVOX-NSCUHMNNSA-N 0.000 description 1
- HPXRVTGHNJAIIH-UHFFFAOYSA-N cyclohexanol Chemical compound OC1CCCCC1 HPXRVTGHNJAIIH-UHFFFAOYSA-N 0.000 description 1
- HAORKNGNJCEJBX-UHFFFAOYSA-N cyprodinil Chemical compound N=1C(C)=CC(C2CC2)=NC=1NC1=CC=CC=C1 HAORKNGNJCEJBX-UHFFFAOYSA-N 0.000 description 1
- 125000002704 decyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 230000018109 developmental process Effects 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
- 150000008056 dicarboxyimides Chemical class 0.000 description 1
- 125000003963 dichloro group Chemical group Cl* 0.000 description 1
- 125000004772 dichloromethyl group Chemical group [H]C(Cl)(Cl)* 0.000 description 1
- YEJGPFZQLRMXOI-PKEIRNPWSA-N diclocymet Chemical compound N#CC(C(C)(C)C)C(=O)N[C@H](C)C1=CC=C(Cl)C=C1Cl YEJGPFZQLRMXOI-PKEIRNPWSA-N 0.000 description 1
- 239000002283 diesel fuel Substances 0.000 description 1
- UZBQIPPOMKBLAS-UHFFFAOYSA-N diethylazanide Chemical compound CC[N-]CC UZBQIPPOMKBLAS-UHFFFAOYSA-N 0.000 description 1
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 1
- BQYJATMQXGBDHF-UHFFFAOYSA-N difenoconazole Chemical compound O1C(C)COC1(C=1C(=CC(OC=2C=CC(Cl)=CC=2)=CC=1)Cl)CN1N=CN=C1 BQYJATMQXGBDHF-UHFFFAOYSA-N 0.000 description 1
- 125000001028 difluoromethyl group Chemical group [H]C(F)(F)* 0.000 description 1
- 229960001760 dimethyl sulfoxide Drugs 0.000 description 1
- WXUZAHCNPWONDH-DYTRJAOYSA-N dimoxystrobin Chemical compound CNC(=O)C(=N\OC)\C1=CC=CC=C1COC1=CC(C)=CC=C1C WXUZAHCNPWONDH-DYTRJAOYSA-N 0.000 description 1
- FBOUIAKEJMZPQG-BLXFFLACSA-N diniconazole-M Chemical compound C1=NC=NN1/C([C@H](O)C(C)(C)C)=C/C1=CC=C(Cl)C=C1Cl FBOUIAKEJMZPQG-BLXFFLACSA-N 0.000 description 1
- 239000013070 direct material Substances 0.000 description 1
- 239000012990 dithiocarbamate Substances 0.000 description 1
- NAGJZTKCGNOGPW-UHFFFAOYSA-N dithiophosphoric acid Chemical compound OP(O)(S)=S NAGJZTKCGNOGPW-UHFFFAOYSA-N 0.000 description 1
- JMXKCYUTURMERF-UHFFFAOYSA-N dodemorph Chemical compound C1C(C)OC(C)CN1C1CCCCCCCCCCC1 JMXKCYUTURMERF-UHFFFAOYSA-N 0.000 description 1
- 239000010459 dolomite Substances 0.000 description 1
- 229910000514 dolomite Inorganic materials 0.000 description 1
- 238000004945 emulsification Methods 0.000 description 1
- 150000002168 ethanoic acid esters Chemical class 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 125000000031 ethylamino group Chemical group [H]C([H])([H])C([H])([H])N([H])[*] 0.000 description 1
- KQTVWCSONPJJPE-UHFFFAOYSA-N etridiazole Chemical compound CCOC1=NC(C(Cl)(Cl)Cl)=NS1 KQTVWCSONPJJPE-UHFFFAOYSA-N 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 235000013312 flour Nutrition 0.000 description 1
- MUJOIMFVNIBMKC-UHFFFAOYSA-N fludioxonil Chemical compound C=12OC(F)(F)OC2=CC=CC=1C1=CNC=C1C#N MUJOIMFVNIBMKC-UHFFFAOYSA-N 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 235000012055 fruits and vegetables Nutrition 0.000 description 1
- 244000000004 fungal plant pathogen Species 0.000 description 1
- 239000003349 gelling agent Substances 0.000 description 1
- 229930182470 glycoside Natural products 0.000 description 1
- 150000002338 glycosides Chemical class 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 125000001188 haloalkyl group Chemical group 0.000 description 1
- 125000005843 halogen group Chemical group 0.000 description 1
- 230000002363 herbicidal effect Effects 0.000 description 1
- 150000007857 hydrazones Chemical class 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- AGKSTYPVMZODRV-UHFFFAOYSA-N imibenconazole Chemical compound C1=CC(Cl)=CC=C1CSC(CN1N=CN=C1)=NC1=CC=C(Cl)C=C1Cl AGKSTYPVMZODRV-UHFFFAOYSA-N 0.000 description 1
- 239000002917 insecticide Substances 0.000 description 1
- ONUFESLQCSAYKA-UHFFFAOYSA-N iprodione Chemical compound O=C1N(C(=O)NC(C)C)CC(=O)N1C1=CC(Cl)=CC(Cl)=C1 ONUFESLQCSAYKA-UHFFFAOYSA-N 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- PVTHJAPFENJVNC-MHRBZPPQSA-N kasugamycin Chemical compound N[C@H]1C[C@H](NC(=N)C(O)=O)[C@@H](C)O[C@@H]1O[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@H](O)[C@@H]1O PVTHJAPFENJVNC-MHRBZPPQSA-N 0.000 description 1
- 239000003350 kerosene Substances 0.000 description 1
- ZOTBXTZVPHCKPN-HTXNQAPBSA-N kresoxim-methyl Chemical compound CO\N=C(\C(=O)OC)C1=CC=CC=C1COC1=CC=CC=C1C ZOTBXTZVPHCKPN-HTXNQAPBSA-N 0.000 description 1
- 239000004571 lime Substances 0.000 description 1
- 239000006028 limestone Substances 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
- BCTQJXQXJVLSIG-UHFFFAOYSA-N mepronil Chemical compound CC(C)OC1=CC=CC(NC(=O)C=2C(=CC=CC=2)C)=C1 BCTQJXQXJVLSIG-UHFFFAOYSA-N 0.000 description 1
- XWPZUHJBOLQNMN-UHFFFAOYSA-N metconazole Chemical compound C1=NC=NN1CC1(O)C(C)(C)CCC1CC1=CC=C(Cl)C=C1 XWPZUHJBOLQNMN-UHFFFAOYSA-N 0.000 description 1
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 1
- OJURWUUOVGOHJZ-UHFFFAOYSA-N methyl 2-[(2-acetyloxyphenyl)methyl-[2-[(2-acetyloxyphenyl)methyl-(2-methoxy-2-oxoethyl)amino]ethyl]amino]acetate Chemical compound C=1C=CC=C(OC(C)=O)C=1CN(CC(=O)OC)CCN(CC(=O)OC)CC1=CC=CC=C1OC(C)=O OJURWUUOVGOHJZ-UHFFFAOYSA-N 0.000 description 1
- 150000004702 methyl esters Chemical class 0.000 description 1
- 229920000257 metiram Polymers 0.000 description 1
- 125000001421 myristyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- YKOMOGKWTRYSHD-UHFFFAOYSA-N n-methoxypentan-3-imine Chemical compound CCC(CC)=NOC YKOMOGKWTRYSHD-UHFFFAOYSA-N 0.000 description 1
- SQDFHQJTAWCFIB-UHFFFAOYSA-N n-methylidenehydroxylamine Chemical compound ON=C SQDFHQJTAWCFIB-UHFFFAOYSA-N 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
- XGXNTJHZPBRBHJ-UHFFFAOYSA-N n-phenylpyrimidin-2-amine Chemical compound N=1C=CC=NC=1NC1=CC=CC=C1 XGXNTJHZPBRBHJ-UHFFFAOYSA-N 0.000 description 1
- 229950002366 nafoxidine Drugs 0.000 description 1
- SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical compound CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 1
- 238000000655 nuclear magnetic resonance spectrum Methods 0.000 description 1
- UWVQIROCRJWDKL-UHFFFAOYSA-N oxadixyl Chemical compound CC=1C=CC=C(C)C=1N(C(=O)COC)N1CCOC1=O UWVQIROCRJWDKL-UHFFFAOYSA-N 0.000 description 1
- AICOOMRHRUFYCM-ZRRPKQBOSA-N oxazine, 1 Chemical compound C([C@@H]1[C@H](C(C[C@]2(C)[C@@H]([C@H](C)N(C)C)[C@H](O)C[C@]21C)=O)CC1=CC2)C[C@H]1[C@@]1(C)[C@H]2N=C(C(C)C)OC1 AICOOMRHRUFYCM-ZRRPKQBOSA-N 0.000 description 1
- 125000000160 oxazolidinyl group Chemical group 0.000 description 1
- 125000000913 palmityl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 230000001717 pathogenic effect Effects 0.000 description 1
- 235000020232 peanut Nutrition 0.000 description 1
- DTGXDHGNUDOWJS-UHFFFAOYSA-N pent-4-enyl butanoate Chemical compound CCCC(=O)OCCCC=C DTGXDHGNUDOWJS-UHFFFAOYSA-N 0.000 description 1
- LKPLKUMXSAEKID-UHFFFAOYSA-N pentachloronitrobenzene Chemical compound [O-][N+](=O)C1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1Cl LKPLKUMXSAEKID-UHFFFAOYSA-N 0.000 description 1
- 125000006340 pentafluoro ethyl group Chemical group FC(F)(F)C(F)(F)* 0.000 description 1
- 229940044654 phenolsulfonic acid Drugs 0.000 description 1
- XKJCHHZQLQNZHY-UHFFFAOYSA-N phthalimide Chemical class C1=CC=C2C(=O)NC(=O)C2=C1 XKJCHHZQLQNZHY-UHFFFAOYSA-N 0.000 description 1
- IBSNKSODLGJUMQ-SDNWHVSQSA-N picoxystrobin Chemical compound CO\C=C(\C(=O)OC)C1=CC=CC=C1COC1=CC=CC(C(F)(F)F)=N1 IBSNKSODLGJUMQ-SDNWHVSQSA-N 0.000 description 1
- 239000002798 polar solvent Substances 0.000 description 1
- 229920001983 poloxamer Polymers 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- QXJKBPAVAHBARF-BETUJISGSA-N procymidone Chemical compound O=C([C@]1(C)C[C@@]1(C1=O)C)N1C1=CC(Cl)=CC(Cl)=C1 QXJKBPAVAHBARF-BETUJISGSA-N 0.000 description 1
- WZZLDXDUQPOXNW-UHFFFAOYSA-N propamocarb Chemical compound CCCOC(=O)NCCCN(C)C WZZLDXDUQPOXNW-UHFFFAOYSA-N 0.000 description 1
- OVPLZYJGTGDFNB-UHFFFAOYSA-N propan-2-yl carbamate Chemical class CC(C)OC(N)=O OVPLZYJGTGDFNB-UHFFFAOYSA-N 0.000 description 1
- WHMZYGMQWIBNOC-UHFFFAOYSA-N propan-2-yl n-(3,4-dimethoxyphenyl)carbamate Chemical compound COC1=CC=C(NC(=O)OC(C)C)C=C1OC WHMZYGMQWIBNOC-UHFFFAOYSA-N 0.000 description 1
- OSFBJERFMQCEQY-UHFFFAOYSA-N propylidene Chemical group [CH]CC OSFBJERFMQCEQY-UHFFFAOYSA-N 0.000 description 1
- FLVBXVXXXMLMOX-UHFFFAOYSA-N proquinazid Chemical compound C1=C(I)C=C2C(=O)N(CCC)C(OCCC)=NC2=C1 FLVBXVXXXMLMOX-UHFFFAOYSA-N 0.000 description 1
- JOOMJVFZQRQWKR-UHFFFAOYSA-N pyrazophos Chemical compound N1=C(C)C(C(=O)OCC)=CN2N=C(OP(=S)(OCC)OCC)C=C21 JOOMJVFZQRQWKR-UHFFFAOYSA-N 0.000 description 1
- 150000003230 pyrimidines Chemical class 0.000 description 1
- 150000004040 pyrrolidinones Chemical class 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 230000004044 response Effects 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 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
- 239000002002 slurry Substances 0.000 description 1
- YZHUMGUJCQRKBT-UHFFFAOYSA-M sodium chlorate Chemical compound [Na+].[O-]Cl(=O)=O YZHUMGUJCQRKBT-UHFFFAOYSA-M 0.000 description 1
- APSBXTVYXVQYAB-UHFFFAOYSA-M sodium docusate Chemical compound [Na+].CCCCC(CC)COC(=O)CC(S([O-])(=O)=O)C(=O)OCC(CC)CCCC APSBXTVYXVQYAB-UHFFFAOYSA-M 0.000 description 1
- 239000011877 solvent mixture Substances 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- PUYXTUJWRLOUCW-UHFFFAOYSA-N spiroxamine Chemical compound O1C(CN(CC)CCC)COC11CCC(C(C)(C)C)CC1 PUYXTUJWRLOUCW-UHFFFAOYSA-N 0.000 description 1
- 230000004763 spore germination Effects 0.000 description 1
- 238000007592 spray painting technique Methods 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 229920002994 synthetic fiber Polymers 0.000 description 1
- 230000009885 systemic effect Effects 0.000 description 1
- CXWXQJXEFPUFDZ-UHFFFAOYSA-N tetralin Chemical compound C1=CC=C2CCCCC2=C1 CXWXQJXEFPUFDZ-UHFFFAOYSA-N 0.000 description 1
- 230000001225 therapeutic effect Effects 0.000 description 1
- YFNCATAIYKQPOO-UHFFFAOYSA-N thiophanate Chemical compound CCOC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OCC YFNCATAIYKQPOO-UHFFFAOYSA-N 0.000 description 1
- 229960002447 thiram Drugs 0.000 description 1
- OBZIQQJJIKNWNO-UHFFFAOYSA-N tolclofos-methyl Chemical compound COP(=S)(OC)OC1=C(Cl)C=C(C)C=C1Cl OBZIQQJJIKNWNO-UHFFFAOYSA-N 0.000 description 1
- 125000003944 tolyl group Chemical group 0.000 description 1
- YWGZBLRRLREJIR-UHFFFAOYSA-N triazole-1-sulfonamide Chemical compound NS(=O)(=O)N1C=CN=N1 YWGZBLRRLREJIR-UHFFFAOYSA-N 0.000 description 1
- 150000003852 triazoles Chemical class 0.000 description 1
- ONCZDRURRATYFI-TVJDWZFNSA-N trifloxystrobin Chemical compound CO\N=C(\C(=O)OC)C1=CC=CC=C1CO\N=C(/C)C1=CC=CC(C(F)(F)F)=C1 ONCZDRURRATYFI-TVJDWZFNSA-N 0.000 description 1
- HSMVPDGQOIQYSR-KGENOOAVSA-N triflumizole Chemical compound C1=CN=CN1C(/COCCC)=N/C1=CC=C(Cl)C=C1C(F)(F)F HSMVPDGQOIQYSR-KGENOOAVSA-N 0.000 description 1
- JARYYMUOCXVXNK-CSLFJTBJSA-N validamycin A Chemical compound N([C@H]1C[C@@H]([C@H]([C@H](O)[C@H]1O)O[C@H]1[C@@H]([C@@H](O)[C@H](O)[C@@H](CO)O1)O)CO)[C@H]1C=C(CO)[C@@H](O)[C@H](O)[C@H]1O JARYYMUOCXVXNK-CSLFJTBJSA-N 0.000 description 1
- 229910052720 vanadium Inorganic materials 0.000 description 1
- 239000011708 vitamin B3 Substances 0.000 description 1
- 235000019160 vitamin B3 Nutrition 0.000 description 1
- 239000004562 water dispersible granule Substances 0.000 description 1
- 239000003021 water soluble solvent Substances 0.000 description 1
- 238000009333 weeding Methods 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
- A01N43/02—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms
- A01N43/24—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with two or more hetero atoms
-
- 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
- A01N47/10—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof
- A01N47/12—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof containing a —O—CO—N< group, or a thio analogue thereof, neither directly attached to a ring nor the nitrogen atom being a member of a heterocyclic ring
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
本发明涉及杀真菌混合物,其以协同增效有效量包含如下化合物作为活性组分:1)式I的氨基甲酸酯肟醚,其中X为N或CH,和2)至少一种选自唑类、嗜球果伞素类、羧酰胺类、杂环化合物、氨基甲酸盐类、胍类、抗菌素类、硝基苯基衍生物、含硫杂环化合物、有机金属化合物、有机磷化合物、有机氯化合物、无机活性化合物、环氟菌胺、清菌脲、甲菌定、乙菌定、呋氨丙灵、苯菌酮和螺茂胺的活性物质II。本发明还涉及一种借助化合物I与活性物质II的混合物防治有害真菌的方法,化合物I与活性物质II在生产所述混合物中的用途以及包含这些混合物的试剂。
Description
本发明涉及杀真菌混合物,其以协同增效有效量包含如下化合物作为活性组分:
1)式I的氨基甲酸酯肟醚:
其中X为N或CH,
和
2)至少一种选自下组的活性化合物II:
A)唑类,例如双苯三唑醇(bitertanol)、糠菌唑(bromuconazole)、环唑醇(cyproconazole)、醚唑(difenoconazole)、烯唑醇(diniconazole)、烯菌灵(enilconazole)、氧唑菌(epoxiconazole)、喹唑菌酮(fluquinconazole)、腈苯唑(fenbuconazole)、氟硅唑(flusilazole)、粉唑醇(flutriafol)、己唑醇(hexaconazole)、酰胺唑(imibenconazole)、环戊唑醇(ipconazole)、环戊唑菌(metconazole)、腈菌唑(myclobutanil)、戊菌唑(penconazole)、丙环唑(propiconazole)、丙硫菌唑(prothioconazole)、硅氟唑(simeconazole)、三唑酮(triadimefon)、唑菌醇(triadimenol)、戊唑醇(tebuconazole)、氟醚唑(tetraconazole)、戊叉唑菌(triticonazole)、丙氯灵(prochloraz)、稻瘟酯(pefurazoate)、烯菌灵(imazalil)、氟菌唑(triflumizole)、氰霜唑(cyazofamid)、苯菌灵(benomyl)、多菌灵(carbendazim)、涕必灵(thiabendazole)、麦穗宁(fuberidazole)、噻唑菌胺(ethaboxam)、氯唑灵(etridiazole)、土菌消(hymexazole),
B)嗜球果伞素类(strobilurins),如腈嘧菌酯(azoxystrobin)、醚菌胺(dimoxystrobin)、烯肟菌酯(enestroburin)、氟嘧菌酯(fluoxastrobin)、亚胺菌(kresoxim-methyl)、叉氨苯酰胺(metominostrobin)、肟醚菌胺(orysastrobin)、啶氧菌酯(picoxystrobin)、唑菌胺酯(pyraclostrobin)、肟菌酯(trifloxystrobin);
C)羧酰胺类,如萎锈灵(carboxin)、苯霜灵(benalaxyl)、啶酰菌胺(boscalid)、环酰菌胺(fenhexamid)、氟酰胺(flutolanil)、呋吡唑灵(furametpyr)、丙氧灭绣胺(mepronil)、甲霜灵(metalaxyl)、精甲霜灵(mefenoxam)、甲呋酰胺(ofurace)、霜灵(oxadixyl)、氧化萎锈灵(oxycarboxin)、吡噻菌胺(penthiopyrad)、溴氟唑菌(thifluzamide)、噻酰菌胺(tiadinil),
3,4-二氯-N-(2-氰基苯基)异噻唑-5-甲酰胺、烯酰吗啉(dimethomorph)、氟吗啉(flumorph),
氟联苯菌(flumetover)、氟吡菌胺(picobenzamid)、苯酰菌胺(zoxamide),氯环丙酰胺(carpropamid)、双氯氰菌胺(diclocymet)、双炔酰菌胺(mandipropamid),
N-(2-{4-[3-(4-氯苯基)丙-2-炔基氧基]-3-甲氧基苯基}乙基)-2-甲磺酰氨基-3-甲基丁酰胺、N-(2-{4-[3-(4-氯苯基)丙-2-炔基氧基]-3-甲氧基苯基}乙基)-2-乙磺酰氨基-3-甲基丁酰胺,
式III的酰胺:
其中各变量和指数如下所定义:
R1和R2相互独立地为氢、卤素、C1-C6烷基或C1-C6卤代烷基、氰基、硝基、甲氧基或三氟甲氧基,条件是R1和R2不同时为氢,和
R3为CF3或CHF2;
D)杂环化合物,如氟啶胺(fluazinam)、啶斑肟(pyrifenox)、磺嘧菌灵(bupirimate)、环丙嘧啶(cyprodinil)、异嘧菌醇(fenarimol)、嘧菌腙(ferimzone)、嘧菌胺(mepanipyrim)、氟苯嘧啶醇(nuarimol)、二甲嘧菌胺(pyrimethanil),
嗪氨灵(triforine),
拌种咯(fenpiclonil)、氟菌(fludioxonil),
4-十二烷基-2,6-二甲基吗啉(aldimorph)、吗菌灵(dodemorph)、丁苯吗啉(fenpropimorph)、克啉菌(tridemorph),
苯锈啶(fenpropidin),
异丙定(iprodione)、杀菌利(procymidone)、烯菌酮(vinclozolin),
唑酮菌(famoxadone)、咪唑菌酮(fenamidone)、异噻菌酮(octhilinone)、噻菌灵(probenazole),
5-氯-7-(4-甲基哌啶-1-基)-6-(2,4,6-三氟苯基)[1,2,4]三唑并[1,5-a]嘧啶,敌菌灵(anilazine)、哒菌清(diclomezine)、咯喹酮(pyroquilon)、丙氧喹啉(proquinazid)、三环唑(tricyclazole),
2-丁氧基-6-碘-3-丙基苯并吡喃-4-酮,
噻二唑素(acibenzolar-S-methyl)、敌菌丹(captafol)、克菌丹(captan)、棉隆(dazomet)、灭菌丹(folpet)、氰菌胺(fenoxanil)、喹氧灵(quinoxyfen),或
N,N-二甲基-3-(3-溴-6-氟-2-甲基吲哚-1-磺酰基)[1,2,4]三唑-1-磺酰胺;E)氨基甲酸盐类,如代森锰锌(mancozeb)、代森锰(maneb)、威百亩(metam)、代森联(metiram)、福美铁(ferbam)、甲基代森锌(propineb)、福美双(thiram)、代森锌(zineb)、福美锌(ziram),
乙霉威(diethofencarb)、异丙菌胺(iprovalicarb)、苯噻菌胺(flubenthiavalicarb)、百维灵(propamocarb),
3-(4-氯苯基)-3-(2-异丙氧基羰基氨基-3-甲基丁酰氨基)丙酸甲酯,
和
F)选自如下的其他杀真菌剂:
胍类:多果定(dodine)、双胍辛醋酸盐(iminoctadine)、双胍盐(guazatine);
抗菌素类:春雷素(kasugamycin)、链霉素(streptomycin)、多氧霉素(polyoxine)、井冈霉素(validamycin A);
硝基苯基衍生物:乐杀螨(binapacryl)、敌螨普(dinocap)、敌螨通(dinobuton),
含硫的杂环基化合物:二噻农(dithianon)、稻瘟灵(isoprothiolane),
有机金属化合物类:三苯锡基盐,如薯瘟锡(fentin acetate),
有机磷化合物:克瘟散(edifenphos)、异稻瘟净(iprobenfos)、藻菌磷(fosetyl)、乙膦铝(fosetyl aluminum)、亚磷酸及其盐、定菌磷(pyrazophos)、甲基立枯磷(tolclofos-methyl);
有机氯化合物:百菌清(chlorothalonil)、抑菌灵(dichlofluanid)、磺菌胺(flusulfamide)、六氯苯(hexachlorobenzene)、四氯苯酞(phthalide)、戊菌隆(pencycuron)、五氯硝基苯(quintozene)、甲基托布津(thiophanate-methyl)、对甲抑菌灵(tolylfluanid),
无机活性化合物:波尔多液(Bordeaux混合物)、醋酸铜、氢氧化铜、王铜、碱式硫酸铜、硫,
其他:环氟菌胺(cyflufenamid)、清菌脲(cymoxanil)、甲菌定(dimethirimol)、乙菌定(ethirimol)、呋氨丙灵(furalaxyl)、苯菌酮(metrafenone)和螺茂胺(spiroxamine)。
此外,本发明涉及一种使用化合物I与活性化合物II的混合物防治有害真菌的方法,化合物I与活性化合物II在制备该类混合物中的用途以及包含这些混合物的组合物。
上面称为组分1的式I肟醚、其制备及其对有害真菌的作用由文献已知(EP-A 1201648)。
上面作为组分2提及的活性化合物II、其制备及其对有害真菌的作用通常是已知的(参见
http://www.hclrss.demon.co.uk/index.html);它们可以市购:
双苯三唑醇,β-([1,1’-联苯]-4-基氧基)-α-(1,1-二甲基乙基)-1H-1,2,4-三唑-1-乙醇(DE 2324020),
糠菌唑,1-[[4-溴-2-(2,4-二氯苯基)四氢-2-呋喃基]甲基]-1H-[1,2,4]-三唑(Proc.1990 Br.Crop.Prot.Conf.-Pests Dis.,第1卷,第459页),
环唑醇,2-(4-氯苯基)-3-环丙基-1-[1,2,4]三唑-1-基丁-2-醇(US 4664696);醚唑,1-{2-[2-氯-4-(4-氯苯氧基)苯基]-4-甲基-[1,3]二氧戊环-2-基甲基}-1H-[1,2,4]三唑(GB-A 2098607);
烯唑醇,(βE)-β-[(2,4-二氯苯基)亚甲基]-α-(1,1-二甲基乙基)-1H-1,2,4-三唑-1-乙醇(Noyaku Kagaku,1983,第8卷,第575页),
烯菌灵(imazalil),1-[2-(2,4-二氯苯基)-2-(2-丙烯氧基)乙基]-1H-咪唑(Fruits,1973,第28卷,第545页),
氧唑菌,(2RS,3SR)-1-[3-(2-氯苯基)-2,3-环氧-2-(4-氟苯基)丙基]-1H-1,2,4-三唑(EP-A 196038);
喹唑菌酮,3-(2,4-二氯苯基)-6-氟-2-[1,2,4]三唑-1-基-3H-喹唑啉-4-酮(Proc.Br.Crop Prot.Conf.-Pests Dis.,5-3,411(1992));
腈苯唑,α-[2-(4-氯苯基)乙基]-α-苯基-1H-1,2,4-三唑-1-丙腈(Proc.1988 Br.Crop Prot.Conf.-Pests Dis.,第1卷,第33页),
氟硅唑,1-{[二(4-氟苯基)甲基硅烷基]甲基}-1H-[1,2,4]三唑(Proc.Br.CropProt.Conf.-Pests Dis.,1,413(1984));
粉唑醇,α-(2-氟苯基)-α-(4-氟苯基)-1H-1,2,4-三唑-1-乙醇(EP 15756),己唑醇,2-(2,4-二氯苯基)-1-[1,2,4]三唑-1-基己-2-醇(CAS RN[79983-71-4]);酰胺唑,N-(2,4-二氯苯基)-1H-1,2,4-三唑-1-乙烷硫代亚胺酸(4-氯苯基)甲基酯(Proc.1988 Br.Crop Prot.Conf.-Pests Dis.,第2卷,第519页),
环戊唑醇,2-[(4-氯苯基)甲基]-5-(1-甲基乙基)-1-(1H-1,2,4-三唑-1-基甲基)环戊醇(EP 267778),
环戊唑菌,5-(4-氯苄基)-2,2-二甲基-1-[1,2,4]三唑-1-基甲基环戊醇(GB 857383);
腈菌唑,2-(4-氯苯基)-2-[1,2,4]三唑-1-基甲基戊腈(CAS RN[88671-89-0]);
戊菌唑,1-[2-(2,4-二氯苯基)戊基]-1H-[1,2,4]三唑(Pesticide Manual,第12版(2000),第712页);
丙环唑,1-[[2-(2,4-二氯苯基)-4-丙基-1,3-二氧戊环-2-基]甲基]-1H-1,2,4-三唑(BE 835579),
丙硫菌唑,2-[2-(1-氯环丙基)-3-(2-氯苯基)-2-羟基丙基]-2,4-二氢[1,2,4]三唑-3-硫酮(WO 96/16048);
硅氟唑,α-(4-氟苯基)-α-[(三甲基甲硅烷基)甲基]-1H-1,2,4-三唑-1-乙醇[CAS RN 149508-90-7],
三唑酮,1-(4-氯苯氧基)-3,3-二甲基-1-(1H-1,2,4-三唑-1-基)-2-丁酮;
唑菌醇,β-(4-氯苯氧基)-α-(1,1-二甲基乙基)-1H-1,2,4-三唑-1-乙醇;
戊唑醇,1-(4-氯苯基)-4,4-二甲基-3-[1,2,4]三唑-1-基甲基戊-3-醇(EP-A 40345);
氟醚唑,1-[2-(2,4-二氯苯基)-3-(1,1,2,2-四氟乙氧基)丙基]-1H-1,2,4-三唑(EP234 242),
戊叉唑菌,(5E)-5-[(4-氯苯基)亚甲基]-2,2-二甲基-1-(1H-1,2,4-三唑-1-基甲基)环戊醇(FR 2641277),
丙氯灵,N-{丙基-[2-(2,4,6-三氯苯氧基)乙基]}咪唑-1-甲酰胺(US 3991071);
稻瘟酯,2-[(2-呋喃基甲基)(1H-咪唑-1-基羰基)氨基]丁酸4-戊烯基酯[CASRN 101903-30-4],
氟菌唑,(4-氯-2-三氟甲基苯基)-(2-丙氧基-1-[1,2,4]三唑-1-基亚乙基)胺(JP-A 79/119462)
氰霜唑,4-氯-2-氰基-N,N-二甲基-5-(4-甲基苯基)-1H-咪唑-1-磺酰胺(CASRN 120116-88-3),
苯菌灵,N-丁基-2-乙酰氨基苯并咪唑-1-甲酰胺(US 3631176);
多菌灵,(1H-苯并咪唑-2-基)氨基甲酸甲酯(US 3657443);
涕必灵,2-(1,3-噻唑-4-基)苯并咪唑(US 3017415),
麦穗宁,2-(2-呋喃基)-1H-苯并咪唑(DE 1209799),
噻唑菌胺,N-(氰基-2-噻吩基甲基)-4-乙基-2-(乙基氨基)-5-噻唑甲酰胺(EP-A 639574),
氯唑灵,
土菌消,5-甲基-1,2-唑-3-醇(JP 518249,JP 532202),
腈嘧菌酯,2-{2-[6-(2-氰基-1-乙烯基戊-1,3-二烯氧基)嘧啶-4-基氧基]苯基}-3-甲氧基丙烯酸甲酯(EP-A 382375),
醚菌胺,(E)-2-(甲氧亚氨基)-N-甲基-2-[α-(2,5-二甲苯氧基)-邻甲苯基]乙酰胺(EP-A 477631);
氟嘧菌酯,(E)-{2-[6-(2-氯苯氧基)-5-氟嘧啶-4-基氧基]苯基}(5,6-二氢-1,4,2-二嗪-3-基)甲酮O-甲基肟(WO 97/27189);
亚胺菌,(E)-甲氧亚氨基[α-(邻甲苯氧基)-邻甲苯基]乙酸甲酯(EP-A 253213);
叉氨苯酰胺,(E)-2-(甲氧亚氨基)-N-甲基-2-(2-苯氧基苯基)乙酰胺(EP-A 398692);
肟醚菌胺,(2E)-2-(甲氧亚氨基)-2-{2-[(3E,5E,6E)-5-(甲氧亚氨基)-4,6-二甲基-2,8-二氧杂-3,7-二氮杂壬-3,6-二烯-1-基]苯基}-N-甲基乙酰胺(WO97/15552);
啶氧菌酯,3-甲氧基-2-[2-(6-三氟甲基吡啶-2-基氧基甲基)苯基]丙烯酸甲酯(EP-A 278595);
唑菌胺酯,N-{2-[1-(4-氯苯基)-1H-吡唑-3-基氧基甲基]苯基}(N-甲氧基)氨基甲酸甲酯(WO-A 96/01256);
肟菌酯,(E)-甲氧亚氨基-{(E)-α-[1-(α,α,α-三氟-间甲苯基)亚乙基氨基氧基]-邻甲基}乙酸甲酯(EP-A 460575);
萎锈灵,5,6-二氢-2-甲基-N-苯基-1,4-氧硫杂芑-3-甲酰胺(US 3249499);
苯霜灵,N-(苯基乙酰基)-N-(2,6-二甲苯基)-DL-丙氨酸甲酯(DE 2903612),
啶酰菌胺,2-氯-N-(4’-氯联苯-2-基)烟酰胺(EP-A 545099);
环酰菌胺,N-(2,3-二氯-4-羟基苯基)-1-甲基环己烷甲酰胺(Proc.Br.CropProt.Conf.-Pests Dis.,1998,第2卷,第327页);
氟酰胺,α,α,α-三氟-3’-异丙氧基-邻甲苯甲酰苯胺(JP 1104514),
呋吡唑灵,5-氯-N-(1,3-二氢-1,1,3-三甲基-4-异苯并呋喃基)-1,3-二甲基-1H-吡唑-4-甲酰胺[CAS RN 123572-88-3],
丙氧灭绣胺,3’-异丙氧基-邻甲苯甲酰苯胺(US 3937840),
甲霜灵,N-(甲氧基乙酰基)-N-(2,6-二甲苯基)-DL-丙氨酸甲酯(GB 1500581);
精甲霜灵,N-(2,6-二甲苯基)-N-(甲氧基乙酰基)-D-丙氨酸甲酯(WO96/01559);
甲呋酰胺,(RS)-α-(2-氯-N-2,6-二甲苯基乙酰胺基)-γ-丁内酯[CAS RN58810-48-3];
霜灵,N-(2,6-二甲基苯基)-2-甲氧基-N-(2-氧代-3-唑烷基)乙酰胺(GB2058059),
氧化萎锈灵,5,6-二氢-2-甲基-1,4-氧硫杂芑-3-甲酰苯胺4,4-二氧化物(US3399214),
吡噻菌胺,N-[2-(1,3-二甲基丁基)-3-噻吩基]-1-甲基-3-(三氟甲基)-1H-吡唑-4-甲酰胺(JP 10130268),
溴氟唑菌,
噻酰菌胺,3’-氯-4,4’-二甲基-1,2,3-噻二唑-5-甲酰苯胺[CAS RN223580-51-6],
烯酰吗啉,3-(4-氯苯基)-3-(3,4-二甲氧基苯基)-1-吗啉-4-基丙烯酮(EP-A 120321);
氟吗啉,3-(4-氟苯基)-3-(3,4-二甲氧基苯基)-1-吗啉-4-基丙烯酮(EP-A 860438);
氟联苯菌,2-(3,4-二甲氧基苯基)-N-乙基-α,α,α-三氟-N-甲基-对甲苯甲酰胺[AGROW No.243,22(1995)],
氟吡菌胺(picobenzamid),2,6-二氯-N-(3-氯-5-三氟甲基吡啶-2-基甲基)苯甲酰胺(WO 99/42447);
苯酰菌胺,(RS)-3,5-二氯-N-(3-氯-1-乙基-1-甲基-2-氧代丙基)-对甲苯甲酰胺[CAS RN 156052-68-5];
氨环丙酰胺,2,2-二氯-N-[1-(4-氯苯基)乙基]-1-乙基-3-甲基环丙烷甲酰胺[CAS RN 104030-54-8],
双氯氰菌胺,2-氰基-N-[(1R)-1-(2,4-二氯苯基)乙基]-3,3-二甲基丁酰胺;
双炔酰菌胺,(RS)-2-(4-氯苯基)-N-[3-甲氧基-4-(丙-2-炔基氧基)苯乙基]-2-(丙-2-炔基氧基)乙酰胺[CAS RN 374726-62-2];
氟啶胺,3-氯-N-[3-氯-2,6-二硝基-4-(三氟甲基)苯基]-5-(三氟甲基)-2-吡啶胺(The Pesticide Manual,publ.The British Crop Protection Council,第10版(1995),第474页);
啶斑肟,1-(2,4-二氯苯基)-2-(3-吡啶基)乙酮O-甲基肟(EP-A 49854),磺嘧菌灵,
环丙嘧啶,(4-环丙基-6-甲基嘧啶-2-基)苯基胺(EP-A 310550);
异嘧菌醇,(4-氯苯基)-(2-氯苯基)嘧啶-5-基甲醇(GB 1218623),
嘧菌腙,(Z)-2’-甲基苯乙酮4,6-二甲基嘧啶-2-基腙;
嘧菌胺,(4-甲基-6-丙-1-炔基嘧啶-2-基)苯基胺(EP-A 224339);
氟苯嘧啶醇,α-(2-氯苯基)-α-(4-氟苯基)-5-嘧啶甲醇(GB 1218623);
二甲嘧菌胺,4,6-二甲基嘧啶-2-基)苯基胺(DD-A 151404);
嗪氨灵,N,N’-{哌嗪-1,4-二基二[(三氯甲基)亚甲基]}二甲酰胺(DE 1901421);
拌种咯,4-(2,3-二氯苯基)-1H-吡咯-3-甲腈(Proc.1988 Br.Crop Prot.Conf.-Pests Dis.,第1卷,第65页);
氟菌,4-(2,2-二氟苯并[1,3]二氧杂环戊烯-4-基)-1H-吡咯-3-甲腈(ThePesticide Manual,publ.The British Crop Protection Council,第10版(1995),第482页);
4-十二烷基-2,6-二甲基吗啉,包含65-75%2,6-二甲基吗啉和25-35%2,5-二甲基吗啉的4-烷基-2,5(或2,6)-二甲基吗啉,其中超过85%为4-十二烷基-2,5(或2,6)-二甲基吗啉且其中“烷基”还可以包括辛基、癸基、十四烷基和十六烷基以及其中顺/反比为1∶1;
吗菌灵,4-环十二烷基-2,6-二甲基吗啉(DE 1198125),
丁苯吗啉,(RS)-顺式4-[3-(4-叔丁基苯基)-2-甲基丙基]-2,6-二甲基吗啉(DE2752096),
克啉菌,2,6-二甲基-4-十三烷基吗啉(DE 1164152),
苯锈啶,(RS)-1-[3-(4-叔丁基苯基)-2-甲基丙基]哌啶(DE 2752096),
异丙定,N-异丙基-3-(3,5-二氯苯基)-2,4-二氧代咪唑烷-1-甲酰胺(GB 1312536);
杀菌利,N-(3,5-二氯苯基)-1,2-二甲基环丙烷-1,2-二甲酰亚胺(US 3903090);
烯菌酮,3-(3,5-二氯苯基)-5-甲基-5-乙烯基唑烷-2,4-二酮(DE-OS2207576);
唑酮菌,(RS)-3-苯胺基-5-甲基-5-(4-苯氧基苯基)-1,3-唑烷-2,4-二酮;
咪唑菌酮,(S)-1-苯胺基-4-甲基-2-甲硫基-4-苯基咪唑啉-5-酮;
异噻菌酮,
噻菌灵,3-烯丙氧基-1,2-苯并噻唑1,1-二氧化物[CAS RN 27605-76-1];
敌菌灵,4,6-二氯-N-(2-氯苯基)-1,3,5-三嗪-2-胺(US 2720480);
哒菌清,6-(3,5-二氯苯基-对甲苯基)哒嗪-3(2H)-酮;
咯喹酮,1,2,5,6-四氢吡咯并[3,2,1-ij]喹啉-4-酮(GB 1394373);
丙氧喹啉,6-碘-2-丙氧基-3-丙基喹唑啉-4(3H)-酮(WO 97/48684);
三环唑,5-甲基-1,2,4-三唑并[3,4-b]苯并噻唑(GB 1419121);
噻二唑素,苯并[1,2,3]噻二唑-7-硫代羰酸甲基酯;
敌菌丹,N-(1,1,2,2-四氯乙硫基)环己-4-烯-1,2-二甲酰亚胺;
克菌丹,2-三氯甲硫基-3a,4,7,7a-四氢异吲哚-1,3-二酮(US 2553770);
棉隆,3,5-二甲基-1,3,5-噻二嗪烷-2-硫酮;
灭菌丹,2-三氯甲硫基异吲哚-1,3-二酮(US 2553770);
氰菌胺,N-(1-氰基-1,2-二甲基丙基)-2-(2,4-二氯苯氧基)丙酰胺(EP-A 262393);
喹氧灵,5,7-二氯-4-(4-氟苯氧基)喹啉(US 5240940);
代森锰锌,亚乙基二(二硫代氨基甲酸)锰锌配合物(US 3379610);
代森锰,亚乙基二(二硫代氨基甲酸)锰(US 2504404);
威百亩,甲基二硫代氨基甲酸(US 2791605);
代森联,亚乙基二(二硫代氨基甲酸)锌氨合物(US 3248400);
甲基代森锌,亚丙基二(二硫代氨基甲酸)锌聚合物(BE 611960);
福美铁,二甲基二硫代氨基甲酸铁(3+)(US 1972961);
福美双,二(二甲基硫代氨基甲酰基)二硫化物(DE 642532);
福美锌,二甲基二硫代氨基甲酸盐[CAS RN 137-30-4];
代森锌,亚乙基二(二硫代氨基甲酸)锌(US 2457674);
乙霉威,3,4-二乙氧基苯胺基甲酸异丙基酯;
异丙菌胺,[(1S)-2-甲基-1-(1-对甲苯基乙基氨基甲酰基)丙基]氨基甲酸异丙基酯(EP-A 472996);
苯噻菌胺(benthiavalicarb),{(S)-1-[(1R)-1-(6-氟苯并噻唑-2-基)乙基氨基甲酰基]-2-甲基丙基}氨基甲酸异丙基酯(JP-A 09/323984);
百维灵,3-(二甲基氨基)丙基氨基甲酸丙基酯(DE 1643040);
多果定,(2,4-二氯苯氧基)乙酸(US 2867562);
双胍盐,包含双胍辛醋酸盐-二(8-胍基辛基)胺的混合物(GB 1114155);
春雷素,1L-1,3,4/2,5,6-1-脱氧-2,3,4,5,6-五羟基环己基-2-氨基-2,3,4,6-四脱氧-4-(α-亚氨基甘氨酰)-α-D-阿拉伯吡喃己糖苷;
链霉素,O-2-脱氧-2-甲基氨基-α-L-吡喃葡糖基-(1→2)-O-5-脱氧-3-C-甲酰基-α-L-呋喃来苏糖基-(1→4)-N1,N3-二脒基-D-链霉胺;
多氧霉素,5-(2-氨基-5-O-氨基甲酰基-2-脱氧-L-木质酰胺基)-1-(5-羧基-1,2,3,4-四氢-2,4-二氧代嘧啶-1-基)-1,5-二脱氧-β-D-呋喃阿洛糖醛酸及其盐;
井冈霉素,
乐杀螨,3-甲基巴豆酸(RS)-2-仲丁基-4,6-二硝基苯基酯;
敌螨普,巴豆酸2,6-二硝基-4-辛基苯基酯和巴豆酸2,4-二硝基-6-辛基苯基酯的混合物,其中“辛基”为1-甲基庚基、1-乙基己基和1-丙基戊基的混合物(US 2526660);
敌螨通,碳酸(RS)-2-仲丁基-4,6-二硝基苯基·异丙基酯;
二噻农,5,10-二氧代-5,10-二氢萘并[2,3-b][1,4]二噻英-2,3-二甲腈(GB857383);
稻瘟灵,吲哚-3-基乙酸[CAS RN 50512-35-1];
薯瘟锡,乙酸三苯基锡;
克瘟散,二硫代磷酸O-乙基S,S-二苯基酯;
异稻瘟净,
藻菌磷、乙膦铝,膦酸乙酯铝盐(FR 2254276);
定菌磷,
甲基立枯磷,硫代磷酸O-2,6-二氯-对甲苯基O,O-二甲基酯(GB 1467561);
百菌清,2,4,5,6-四氯间苯二甲腈(US 3290353);
抑菌灵,N-二氯一氟甲硫基-N’,N’-二甲基-N-苯基磺酰胺(DE 1193498);
磺菌胺,
六氯苯,
四氯苯酞,
戊菌隆,1-(4-氯苄基)-1-环戊基-3-苯基脲(DE 2732257);
五氯硝基苯,五氯硝基苯(DE 682048);
甲基托布津,1,2-亚苯基二(亚氨基硫代羰基)二(氨基甲酸二甲酯)(DE-OS 1930540);
对甲抑菌灵,N-二氯一氟甲硫基-N’,N’-二甲基-N-对甲苯基磺酰胺(DE 1193498);
环氟菌胺,(Z)-N-[α-(环丙基甲氧亚氨基)-2,3-二氟-6-(三氟甲基)苄基]-2-苯基乙酰胺(WO 96/19442);
清菌脲,1-(2-氰基-2-甲氧亚氨基乙酰基)-3-乙基脲(US 3957847);
甲菌定,
乙菌定,
呋氨丙灵,
苯菌酮,3’-溴-2,3,4,6’-四甲氧基-2’,6-二甲基二苯甲酮(US 5 945 567);
螺茂胺,(8-叔丁基-1,4-二氧杂螺[4.5]癸-2-基)二乙基胺(EP-A 281842)。
根据IUPAC命名的化合物、其制备及其杀真菌作用同样是已知的:
5-氯-7-(4-甲基哌啶-1-基)-6-(2,4,6-三氟苯基)-[1,2,4]三唑并[1,5-a]嘧啶(WO98/46608),
3,4-二氯-N-(2-氰基苯基)异噻唑-5-甲酰胺(WO 99/24413),
N-(2-{4-[3-(4-氯苯基)丙-2-炔基氧基]-3-甲氧基苯基}乙基)-2-甲磺酰氨基-3-甲基丁酰胺、N-(2-{4-[3-(4-氯苯基)丙-2-炔基氧基]-3-甲氧基苯基}乙基)-2-乙磺酰氨基-3-甲基丁酰胺(WO 04/049804),
R:甲基(II-A)或乙基(II-B);
式III的酰胺(WO 03/066609),
式IV的2-丁氧基-6-碘-3-丙基苯并吡喃-4-酮(WO 03/14103),
式V的N,N-二甲基-3-(3-溴-6-氟-2-甲基吲哚-1-磺酰基)-[1,2,4]三唑-1-磺酰胺(WO 03/053145),
式VI的3-(4-氯苯基)-3-(2-异丙氧基羰基氨基-3-甲基丁酰氨基)丙酸甲酯(EP-A 1028125):
为了降低已知化合物的施用率并拓宽其活性谱,本发明的目的是提供在活性化合物的施用总量降低下对有害真菌,尤其是对某些适应症具有改进活性的混合物。
我们发现该目的由开头所定义的混合物实现。此外,我们发现与单一化合物相比,同时,即联合或分开施用化合物I和活性化合物II或依次施用化合物I和活性化合物II可以更好地防治有害真菌(协同增效混合物)。化合物I可以用作大量不同活性化合物的协同增效剂。同时,即联合或分开使用化合物I和活性化合物II以超加和方式增加了杀真菌效力。
化合物I和活性化合物II的混合物,或同时,即联合或分开使用的化合物I和活性化合物II对宽范围的植物病原性真菌,尤其是选自子囊菌纲(Ascomycetes)、半知菌纲(Deuteromycetes)、卵菌纲(Oomycetes)和担子菌纲(Basidiomycetes)的真菌具有显著效力。它们中的一些起内吸作用且可以作为叶面和土壤作用杀真菌剂用于作物保护中。
它们对在各种作物植物如香蕉、棉花、蔬菜品种(例如黄瓜、豆类和葫芦科植物)、大麦、禾草、燕麦、咖啡、土豆、玉米、水果品种、稻、黑麦、大豆、西红柿、葡萄藤、小麦、观赏植物、甘蔗以及大量种子中防治大量真菌尤其重要。
它们有利地适于防治下列植物病原性真菌:禾谷类中的禾白粉菌(Blumeria graminis)(白粉病),葫芦科植物上的二孢白粉菌(Erysiphecichoracearum)和单丝壳白粉菌(Sphaerotheca fuliginea),苹果上的苹果白粉病菌(Podosphaera leucotricha),葡萄藤上的葡萄钩丝壳菌(Uncinulanecator),禾谷类上的柄锈菌(Puccinia)属,棉花、稻和草坪上的丝核菌(Rhizoctonia)属,禾谷类和甘蔗上的黑粉菌(Ustilago)属,苹果上的黑星病菌(Venturia inaequalis),禾谷类、稻和草坪中的平脐蠕孢(Bipolaris)属和内脐蠕孢(Drechslera)属,小麦上的壳针孢(Septoria)属,草莓、蔬菜、观赏植物和葡萄藤上的灰葡萄孢(Botrytis cinerea),香蕉、花生和禾谷类上的球腔菌(Mycosphaerella)属,小麦和大麦上的眼斑病菌(Pseudocercosporellaherpotrichoides),稻上的稻瘟病菌(Pyricularia oryzae),土豆和西红柿上的致病疫霉(Phytophthora infestans),葫芦科植物和啤酒花上的假霜霉(Pseudoperonospora)属,葡萄藤上的葡萄生单轴霉(Plasmopara viticola),水果和蔬菜上的链格孢(Alternaria)属,以及镰孢霉(Fusarium)属和轮枝孢(Verticillium)属。
化合物I和活性化合物II的混合物尤其适合防治灰霉菌(Botrytis)属有害真菌。
化合物I和活性化合物II可以同时,即联合或分开施用,或依次施用,在分开施用时施用顺序通常对防治措施的结果没有任何影响。
在对式III所给符号的定义中,使用代表下列取代基的集合性术语:卤素:氟、氯、溴和碘;
烷基:具有1-6个碳原子的饱和直链或支化烃基,例如C1-C4烷基,如甲基、乙基、丙基、1-甲基乙基、丁基、1-甲基丙基、2-甲基丙基、1,1-二甲基乙基;
卤代烷基:具有1-6个碳原子的直链或支化烷基,其中这些基团中的部分或所有氢原子可以被上述卤原子替换:尤其是C1-C2卤代烷基,如氯甲基、溴甲基、二氯甲基、三氯甲基、氟甲基、二氟甲基、三氟甲基、氯氟甲基、二氯一氟甲基、一氯二氟甲基、1-氯乙基、1-溴乙基、1-氟乙基、2-氟乙基、2,2-二氟乙基、2,2,2-三氟乙基、2-氯-2-氟乙基、2-氯-2,2-二氟乙基、2,2-二氯-2-氟乙基、2,2,2-三氯乙基或五氟乙基。
式I表示其中X为N(I-A)或CH(I-B)的化合物。
本发明的一个实施方案涉及化合物I-A与活性化合物II的混合物。
本发明的另一实施方案涉及化合物I-B与活性化合物II的混合物。
考虑到式III的酰胺在本发明混合物中的应用,下列式IIIa-IIIf的化合物是特别合适的:
其中特别优选式IIId化合物。尤其优选的是汇编在下表中的化合物:
表1
化合物1.1-1.22:其中R1为氟且R2和R3的组合在每种情况下为表A的一行的式IIIa化合物
表2
化合物2.1-2.22:其中R1为氯且R2和R3的组合在每种情况下为表A的一行的式IIIa化合物
表3
化合物3.1-3.22:其中R1为溴且R2和R3的组合在每种情况下为表A的一行的式IIIa化合物
表4
化合物4.1-4.22:其中R1为碘且R2和R3的组合在每种情况下为表A的一行的式IIIa化合物
表5
化合物5.1-5.22:其中R1为甲基且R2和R3的组合在每种情况下为表A的一行的式IIIa化合物
表6
化合物6.1-6.22:其中R1为甲氧基且R2和R3的组合在每种情况下为表A的一行的式IIIa化合物
表7
化合物7.1-7.22:其中R1为三氟甲基且R2和R3的组合在每种情况下为表A的一行的式IIIa化合物
表8
化合物8.1-8.22:其中R1为三氟甲氧基且R2和R3的组合在每种情况下为表A的一行的式IIIa化合物
表9
化合物9.1-9.22:其中R1为氰基且R2和R3的组合在每种情况下为表A的一行的式IIIa化合物
表10
化合物10.1-10.22:其中R1为硝基且R2和R3的组合在每种情况下为表A的一行的式IIIa化合物
表11
化合物11.1-11.20:其中R1为氢且R2和R3的组合在每种情况下为表A的第2-21行之一的式IIIa化合物
表12
化合物12.1-12.22:其中R1为氟且R2和R3的组合在每种情况下为表A的一行的式IIIb化合物
表13
化合物13.1-13.22:其中R1为氯且R2和R3的组合在每种情况下为表A的一行的式IIIb化合物
表14
化合物14.1-14.22:其中R1为溴且R2和R3的组合在每种情况下为表A的一行的式IIIb化合物
表15
化合物15.1-15.22:其中R1为碘且R2和R3的组合在每种情况下为表A的一行的式IIIb化合物
表16
化合物16.1-16.22:其中R1为甲基且R2和R3的组合在每种情况下为表A的一行的式IIIb化合物
表17
化合物17.1-17.22:其中R1为甲氧基且R2和R3的组合在每种情况下为表A的一行的式IIIb化合物
表18
化合物18.1-18.22:其中R1为三氟甲基且R2和R3的组合在每种情况下为表A的一行的式IIIb化合物
表19
化合物19.1-19.22:其中R1为三氟甲氧基且R2和R3的组合在每种情况下为表A的一行的式IIIb化合物
表20
化合物20.1-20.22:其中R1为氰基且R2和R3的组合在每种情况下为表A的一行的式IIIb化合物
表21
化合物21.1-21.22:其中R1为硝基且R2和R3的组合在每种情况下为表A的一行的式IIIb化合物
表22
化合物22.1-22.20:其中R1为氢且R2和R3的组合在每种情况下为表A的第2-21行之一的式IIIb化合物
表23
化合物23.1-23.22:其中R1为氟且R2和R3的组合在每种情况下为表A的一行的式IIIc化合物
表24
化合物24.1-24.22:其中R1为氯且R2和R3的组合在每种情况下为表A的一行的式IIIc化合物
表25
化合物25.1-25.22:其中R1为溴且R2和R3的组合在每种情况下为表A的一行的式IIIc化合物
表26
化合物26.1-26.22:其中R1为碘且R2和R3的组合在每种情况下为表A的一行的式IIIc化合物
表27
化合物27.1-27.22:其中R1为甲基且R2和R3的组合在每种情况下为表A的一行的式IIIc化合物
表28
化合物28.1-28.22:其中R1为甲氧基且R2和R3的组合在每种情况下为表A的一行的式IIIc化合物
表29
化合物29.1-29.22:其中R1为三氟甲基且R2和R3的组合在每种情况下为表A的一行的式IIIc化合物
表30
化合物30.1-30.22:其中R1为三氟甲氧基且R2和R3的组合在每种情况下为表A的一行的式IIIc化合物
表31
化合物31.1-31.22:其中R1为氰基且R2和R3的组合在每种情况下为表A的一行的式IIIc化合物
表32
化合物32.1-32.22:其中R1为硝基且R2和R3的组合在每种情况下为表A的一行的式IIIc化合物
表34
化合物34.1-34.22:其中R1为氟且R2和R3的组合在每种情况下为表A的一行的式IIId化合物
表35
化合物35.1-35.22:其中R1为氯且R2和R3的组合在每种情况下为表A的一行的式IIId化合物
表36
化合物36.1-36.22:其中R1为溴且R2和R3的组合在每种情况下为表A的一行的式IIId化合物
表37
化合物37.1-37.22:其中R1为碘且R2和R3的组合在每种情况下为表A的一行的式IIId化合物
表38
化合物38.1-38.22:其中R1为甲基且R2和R3的组合在每种情况下为表A的一行的式IIId化合物
表39
化合物39.1-39.22:其中R1为甲氧基且R2和R3的组合在每种情况下为表A的一行的式IIId化合物
表40
化合物40.1-40.22:其中R1为三氟甲基且R2和R3的组合在每种情况下为表A的一行的式IIId化合物
表41
化合物41.1-41.22:其中R1为三氟甲氧基且R2和R3的组合在每种情况下为表A的一行的式IIId化合物
表42
化合物42.1-42.22:其中R1为氰基且R2和R3的组合在每种情况下为表A的一行的式IIId化合物
表43
化合物43.1-43.22:其中R1为硝基且R2和R3的组合在每种情况下为表A的一行的式IIId化合物
表44
化合物44.1-44.20:其中R1为氢且R2和R3的组合在每种情况下为表A的第2-21行之一的式IIId化合物
表45
化合物45.1-45.22:其中R1为氟且R2和R3的组合在每种情况下为表A的一行的式IIIe化合物
表46
化合物46.1-46.22:其中R1为氯且R2和R3的组合在每种情况下为表A的一行的式IIIe化合物
表47
化合物47.1-47.22:其中R1为溴且R2和R3的组合在每种情况下为表A的一行的式IIIe化合物
表48
化合物48.1-48.22:其中R1为碘且R2和R3的组合在每种情况下为表A的一行的式IIIe化合物
表49
化合物49.1-49.22:其中R1为甲基且R2和R3的组合在每种情况下为表A的一行的式IIIe化合物
表50
化合物50.1-50.22:其中R1为甲氧基且R2和R3的组合在每种情况下为表A的一行的式IIIe化合物
表51
化合物51.1-51.22:其中R1为三氟甲基且R2和R3的组合在每种情况下为表A的一行的式IIIe化合物
表52
化合物52.1-52.22:其中R1为三氟甲RNU氧基且R2和R3的组合在每种情况下为表A的一行的式IIIe化合物
表53
化合物53.1-53.22:其中R1为氰基且R2和R3的组合在每种情况下为表A的一行的式IIIe化合物
表54
化合物54.1-54.22:其中R1为硝基且R2和R3的组合在每种情况下为表A的一行的式IIIe化合物
表56
化合物56.1-56.22:其中R1为氟且R2和R3的组合在每种情况下为表A的一行的式HIf化合物
表57
化合物57.1-57.22:其中R1为氯且R2和R3的组合在每种情况下为表A的一行的式IIIf化合物
表58
化合物58.1-58.22:其中R1为溴且R2和R3的组合在每种情况下为表A的一行的式IIIf化合物
表59
化合物59.1-59.22:其中R1为碘且R2和R3的组合在每种情况下为表A的一行的式IIIf化合物
表60
化合物60.1-60.22:其中R1为甲基且R2和R3的组合在每种情况下为表A的一行的式IIIf化合物
表61
化合物61.1-61.22:其中R1为甲氧基且R2和R3的组合在每种情况下为表A的一行的式IIIf化合物
表62
化合物62.1-62.22:其中R1为三氟甲基且R2和R3的组合在每种情况下为表A的一行的式IIIf化合物
表63
化合物63.1-63.22:其中R1为三氟甲氧基且R2和R3的组合在每种情况下为表A的一行的式IIIf化合物
表64
化合物64.1-64.22:其中R1为氰基且R2和R3的组合在每种情况下为表A的一行的式IIIf化合物
表65
化合物65.1-65.22:其中R1为硝基且R2和R3的组合在每种情况下为表A的一行的式IIIf化合物
表66
化合物66.1-66.20:其中R1为氢且R2和R3的组合在每种情况下为表A的第2-21行之一的式IIIf化合物
表A
序号 | R2 | R3 |
1 | H | CF3 |
2 | F | CF3 |
3 | Cl | CF3 |
4 | Br | CF3 |
5 | I | CF3 |
6 | CH3 | CF3 |
7 | OCH3 | CF3 |
8 | CF3 | CF3 |
9 | OCF3 | CF3 |
10 | CN | CF3 |
11 | NO2 | CF3 |
12 | F | CHF2 |
13 | Cl | CHF2 |
14 | Br | CHF2 |
15 | I | CHF2 |
16 | CH3 | CHF2 |
17 | OCH3 | CHF2 |
18 | CF3 | CHF2 |
19 | OCF3 | CHF2 |
20 | CN | CHF2 |
21 | NO2 | CHF2 |
22 | H | CHF2 |
本发明混合物的优选实施方案涉及式I化合物与选自下组的活性化合物的组合:
二硫代氨基甲酸盐,尤其是代森锰锌、甲基代森锌、福美双,
苯并咪唑类,尤其是苯菌灵、托布津、多菌灵,
二羧酰亚胺类,尤其是异丙定、杀菌利、烯菌酮、乙菌利(chlozolinate),
邻苯二甲酰亚胺类,尤其是克菌丹、百菌清、灭菌丹,
苯胺基嘧啶类,尤其是环丙嘧啶、二甲嘧菌胺、嘧菌胺,
三唑类,尤其是戊唑醇、醚唑、环唑醇、腈菌唑,
羧酰苯胺类,尤其是环酰菌胺、苯霜灵、啶酰菌胺、吡噻菌胺,
式III的酰替苯胺类,式IV的化合物,
有机氯化合物,尤其是抑菌灵、百菌清、对甲抑菌灵(tolyfluanid),
氨基甲酸盐类,尤其是乙霉威,
含氮的杂环基化合物,尤其是氟菌、氟啶胺,
嗜球果伞素类,尤其是亚胺菌、唑菌胺酯、腈嘧菌酯、肟菌酯、烯肟菌酯、啶氧菌酯、氟嘧菌酯,
有机锡化合物,尤其是薯瘟锡,以及尤其是
5-氯-7-(4-甲基哌啶-1-基)-6-(2,4,6-三氟苯基)-[1,2,4]三唑并[1,5-a]嘧啶。
制备混合物时,优选使用纯活性化合物,可以根据需要向其中加入对抗有害真菌或其他害虫如昆虫、蜘蛛或线虫的其他活性化合物或除草或生长调节活性化合物或肥料作为其他活性组分。
通常使用化合物I与一种活性化合物II的混合物。然而,在某些情况下化合物I与两种或合适的话多种活性组分的混合物可能是有利的。
在上述意义上合适的其他活性组分尤其为在开头所提到的活性化合物II,尤其是上述优选的活性化合物。
化合物I和活性化合物II通常以100∶1-1∶100,优选20∶1-1∶20,尤其是10∶1-1∶10的重量比使用。
需要的话,可以将其他活性组分以20∶1-1∶20的比例加入化合物I中。
取决于化合物的类型和所需效果,本发明混合物的施用率为5-2000g/ha,优选50-900g/ha,尤其是50-750g/ha。
相应地,化合物I的施用率通常为1-1000g/ha,优选10-900g/ha,尤其是20-750g/ha。
相应地,活性化合物II的施用率通常为1-2000g/ha,优选10-900g/ha,尤其是40-500g/ha。
在种子处理中,混合物的施用率通常为1-1000g/100kg种子,优选1-750g/100kg种子,尤其是5-500g/100kg种子。
防治有害真菌的方法通过在植物播种之前或之后或在它们出苗之前或之后对种子、植物或土壤喷雾或撒粉而分开或联合施用化合物I和活性化合物II,或施用化合物I和活性化合物II的混合物而进行。
可将本发明的混合物或化合物I和活性化合物II转化成常规配制剂,例如溶液、乳液、悬浮液、粉剂、粉末、糊和颗粒。使用形式取决于特定的意欲目的;在每种情况下,应确保本发明化合物精细且均匀地分布。
配制剂以已知方式制备,例如通过将活性化合物与溶剂和/或载体混合而制备,若需要的话使用乳化剂和分散剂。适于该目的的溶剂/助剂主要为:
-水、芳族溶剂(如Solvesso产品、二甲苯)、石蜡(如矿物油馏分)、醇类(如甲醇、丁醇、戊醇、苄醇)、酮类(如环己酮、γ-丁内酯)、吡咯烷酮(NMP、NOP)、乙酸酯(乙二醇二乙酸酯)、二元醇、脂肪酸二甲基酰胺、脂肪酸及脂肪酸酯。原则上还可以使用溶剂混合物。
-载体如磨碎的天然矿物(如高岭土、粘土、滑石、白垩)和磨碎的合成矿物(如高度分散的硅酸、硅酸盐);乳化剂如非离子和阴离子乳化剂(如聚氧乙烯脂肪醇醚、烷基磺酸盐和芳基磺酸盐)以及分散剂如木素亚硫酸盐废液和甲基纤维素。
适合用作表面活性剂的是木素磺酸、萘磺酸、苯酚磺酸、二丁基萘磺酸的碱金属盐、碱土金属盐和铵盐,烷基芳基磺酸盐,烷基硫酸盐,烷基磺酸盐,脂肪醇硫酸盐,脂肪酸和硫酸化脂肪醇乙二醇醚,此外还有磺化萘与甲醛的缩合物和萘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,乙氧基化异辛基酚、辛基酚、壬基酚,烷基苯基聚乙二醇醚,三丁基苯基聚乙二醇醚,三硬脂基苯基聚乙二醇醚,烷基芳基聚醚醇,醇和脂肪醇/氧化乙烯缩合物,乙氧基化蓖麻油,聚氧乙烯烷基醚,乙氧基化聚氧丙烯,月桂醇聚乙二醇醚缩醛,山梨醇酯,木素亚硫酸盐废液和甲基纤维素。
适于制备可直接喷雾溶液、乳液、糊或油分散体的物质为中至高沸点的矿物油馏分如煤油或柴油,还有煤焦油和植物或动物来源的油,脂族、环状和芳族烃如甲苯、二甲苯、石蜡、四氢化萘、烷基化萘或其衍生物,甲醇,乙醇,丙醇,丁醇,环己醇,环己酮,异佛尔酮,强极性溶剂如二甲亚砜、N-甲基吡咯烷酮和水。
粉末、撒播用材料和可撒粉产品可以通过将活性物质与固体载体混合或一起研磨来制备。
颗粒如涂敷颗粒、浸渍颗粒和均质颗粒可以通过使活性化合物与固体载体粘附而制备。固体载体实例为矿土如硅胶、硅酸盐、滑石、高岭土、活性粘土(attaclay)、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、尿素以及植物来源的产品如谷粉、树皮粉、木粉和坚果壳粉,纤维素粉和其它固体载体。
配制剂通常包含0.01-95重量%,优选0.1-90重量%的活性化合物。活性化合物以90-100%,优选95-100%的纯度(根据NMR谱)使用。
对于种子处理,所述配制剂在稀释2-10倍后在即用制剂中给出0.01-60重量%,优选0.1-40重量%的活性化合物浓度。
下列为本发明的配制剂实例:
1.用水稀释的产品
A水溶性浓缩物(SL、LS)
将10重量份活性化合物溶于90重量份水或水溶性溶剂中。或者,加入湿润剂或其它助剂。活性化合物经水稀释溶解。以此方式得到活性化合物含量为10重量%的配制剂。
B分散性浓缩物(DC)
将20重量份活性化合物溶于70重量份环己酮中并加入10重量份分散剂如聚乙烯基吡咯烷酮。用水稀释得到分散体。活性化合物含量为20重量%。
C可乳化的浓缩物(EC)
将15重量份活性化合物溶于75重量份二甲苯中并加入十二烷基苯磺酸钙和蓖麻油乙氧基化物(在每种情况下为5重量份)。用水稀释得到乳液。该配制剂的活性化合物含量为15重量%。
D乳液(EW、EO、ES)
将25重量份活性化合物溶于35重量份二甲苯中并加入十二烷基苯磺酸钙和蓖麻油乙氧基化物(在每种情况下为5重量份)。借助乳化机(例如Ultraturrax)将该混合物加入30重量份水中并制成均相乳液。用水稀释得到乳液。该配制剂的活性化合物含量为25重量%。
E悬浮液(SC、OD、FS)
在搅拌的球磨机中,将20重量份活性化合物粉碎并加入10重量份分散剂和湿润剂以及70重量份水或有机溶剂,得到细碎活性化合物悬浮液。用水稀释得到稳定的活性化合物悬浮液。该配制剂中的活性化合物含量为20重量%。
F水分散性颗粒和水溶性颗粒(WG、SG)
将50重量份活性化合物细碎研磨并加入50重量份分散剂和湿润剂,借助工业装置(如挤出机、喷雾塔、流化床)将其制成水分散性或水溶性颗粒。用水稀释得到稳定的活性化合物分散体或溶液。该配制剂的活性化合物含量为50重量%。
G水分散性粉末和水溶性粉末(WP、SP、SS、WS)
将75重量份活性化合物在转子-定子磨机中研磨并加入25重量份分散剂、湿润剂和硅胶。用水稀释得到稳定的活性化合物分散体或溶液。该配制剂的活性化合物含量为75重量%。
H凝胶配制剂
在珠磨机中将20重量份活性化合物、10重量份分散剂、1重量份胶凝剂和70重量份水或有机溶剂研磨成细悬浮液。用水稀释得到活性化合物含量为20重量%的稳定悬浮液。
2.不经稀释而施用的产品
I粉剂(DP、DS)
将5重量份活性化合物细碎研磨并与95重量份细碎高岭土充分混合。这得到活性化合物含量为5重量%的可撒粉产品。
J颗粒(GR、FG、GG、MG)
将0.5重量份活性化合物细碎研磨并结合95.5重量份载体。现行方法是挤出、喷雾干燥和流化床方法。得到不经稀释而施用的活性化合物含量为0.5重量%的颗粒。
K ULV溶液(UL)
将10重量份活性化合物溶于90重量份有机溶剂如二甲苯中,得到不经稀释而施用的活性化合物含量为10重量%的产品。
对于种子处理,通常利用水溶性浓缩物(LS)、悬浮液(FS)、粉剂(DS)、水分散性和水溶性粉末(WS、SS)、乳液(ES)、可乳化的浓缩物(EC)和凝胶配制剂(GF)。这些配制剂可以不经稀释或优选稀释后施用于种子上。可以在播种前施用。
优选将FS配制剂用于种子处理。该类配制剂通常包含1-800g/L活性物质、1-200g/L表面活性剂、0-200g/L防冻剂、0-400g/L粘合剂、0-200g/L着色剂和溶剂,优选水。
活性化合物可以直接、以其配制剂形式或由其制备的施用形式(如可直接喷雾溶液、粉末、悬浮液或分散体、乳液、油分散体、糊、可撒粉产品、撒播用材料或颗粒形式),借助喷雾、雾化、撒粉、撒播或浇灌来使用。使用形式完全取决于意欲的目的;它们应在每种情况下确保本发明活性化合物的最佳可能分布。
含水使用形式可通过加入水由乳液浓缩物、糊或可湿性粉末(可喷雾粉末、油分散体)制备。为制备乳液、糊或油分散体,可借助湿润剂、增粘剂、分散剂或乳化剂将该物质直接或溶于油或溶剂中后在水中均化。然而,还可以制备由活性物质、湿润剂、增粘剂、分散剂或乳化剂以及合适的话溶剂或油组成的浓缩物,这些浓缩物适于用水稀释。
即用制剂中的活性化合物浓度可在较宽范围内变化。它们通常为0.0001-10%,优选0.01-1%。
活性化合物也可成功用于超低容量法(ULV),其中可以施用包含超过95重量%活性化合物的配制剂,或甚至施用不含添加剂的活性化合物。
各种类型的油、湿润剂、辅助剂、除草剂、杀真菌剂、其它杀虫剂或杀菌剂都可加入活性化合物中,甚至若合适的话,恰在紧邻施用前加入(桶混合)。这些试剂通常可与本发明组合物以1∶100-100∶1,优选1∶10-10∶1的重量比混合。
在这方面合适的辅助剂尤其是有机改性的聚硅氧烷,例如Break ThruS 240;醇烷氧基化物,例如Atplus 245、Atplus MBA 1303、PlurafacLF 300和Lutensol ON 30;EO/PO嵌段聚合物,例如Pluronic RPE 2035和Genapol B;醇乙氧基化物,例如Lutensol XP 80;以及磺基琥珀酸二辛酯钠,例如Leophen RA。
化合物I和II或混合物或对应的配制剂通过用杀真菌有效量的混合物或在分开施用的情况下化合物I和II处理有害真菌或需要防止它们的植物、种子、土壤、区域、材料或空间而施用。可以在有害真菌侵染之前或之后施用。
化合物和混合物的杀真菌效果可通过下列试验证实:
使用溶剂/乳化剂体积比为99∶1的丙酮和/或DMSO与乳化剂UniperolEL(基于乙氧基化烷基酚的具有乳化和分散作用的润湿剂)的混合物将活性化合物单独或一起制备成包含25mg活性化合物并配成10ml的储备溶液。然后用水将该混合物配成100ml。使用所述溶剂/乳化剂/水混合物将该储备溶液稀释至下述活性物质浓度。
将肉眼测定的侵染叶面积百分数转化成效力,以相对于未处理对照的%表示:
使用Abbot公式按如下计算效力(E):
E=(1-α/β)·100
α对应于处理植物的真菌侵染百分数,和
β对应于未处理(对照)植物的真菌侵染百分数。
效力为0表示处理植物的侵染水平相当于未处理的对照植物;效力为100表示处理植物未受侵染。
活性化合物组合的预期效力使用Colby公式[Colby,S.R.,“计算除草剂组合的协同增效和拮抗响应”,Weeds(杂草),15,20-22,1967]确定并与观察的效力比较。
Colby公式:E=x+y-x·y/100
E使用浓度为a和b的活性化合物A和B的混合物时的预期效力,以相对于未处理对照的%表示,
x使用浓度为a的活性化合物A时的效力,以相对于未处理对照的%表示,
y使用浓度为b的活性化合物B时的效力,以相对于未处理对照的%表示。温室试验
应用实施例1-对柿子椒上的灰葡萄孢的活性
将栽培品种为“Neusiedler Ideal Elite”的柿子椒秧苗在充分发育出2-3片叶后用活性化合物浓度如下所述的含水悬浮液喷雾至滴流点。第二天将已处理植物用在浓度为2%的生物麦芽溶液中含有1.7×106个孢子/ml的灰葡萄孢的孢子悬浮液接种。然后将试验植物置于22-24℃和高大气湿度的黑暗气候调节室中。5天后可肉眼测定叶子上的真菌侵染程度的百分数。
序号 | 活性化合物 | 浓度[ppm] | 比例 | 观察的活性(%) | 根据Colby计算的活性(%) |
1 | -(对照) | - | 0(100%侵染) | ||
2 | I-B | 63 | 20 |
序号 | 活性化合物 | 浓度[ppm] | 比例 | 观察的活性(%) | 根据Colby计算的活性(%) |
16 | 10 | ||||
3 | 二噻农(F11) | 63 | 10 | ||
4 | I-B+F11 | 63+63 | 1∶1 | 60 | 28 |
5 | I-B+F11 | 16+63 | 1∶4 | 50 | 19 |
应用实施例2-对小麦隐匿柄锈菌(Puccinia recondita)引起的小麦叶锈病的治疗活性
将栽培品种为“Kanzler”的盆栽小麦秧苗的叶子用小麦叶锈病菌(小麦隐匿柄锈菌)的孢子悬浮液接种。然后在20-22℃下将盆放置在高大气湿度(90-95%)的室中24小时。在此期间孢子萌发并且芽管穿透到叶组织中。第二天将侵染的植物用活性化合物浓度如下所述的上述活性化合物溶液喷雾至滴流点。在喷雾涂层干燥之后,将试验植物在温度为20-22℃和相对大气湿度为65-70%的温室中栽培7天。然后测定锈病真菌在叶子上的发展程度。
序号 | 活性化合物 | 浓度[ppm] | 比例 | 观察的活性(%) | 根据Colby计算的活性(%) |
6 | -(对照) | - | 0(85%侵染) | ||
7 | I-B | 16 | 6 | ||
8 | 亚胺菌(B5) | 634 | 180 | ||
9 | 啶酰菌胺(C3) | 16 | 0 | ||
10 | 甲霜灵(C8) | 16 | 0 | ||
11 | 烯酰吗啉(C17) | 82 | 00 | ||
12 | I-B+B5 | 16+63 | 1∶4 | 99 | 22 |
13 | I-B+C3 | 16+16 | 1∶1 | 82 | 6 |
14 | I-B+C8 | 16+16 | 1∶1 | 94 | 6 |
15 | I-B+C17 | 16+8 | 2∶1 | 92 | 6 |
16 | I-B+C17 | 16+2 | 8∶1 | 76 | 6 |
微滴定板试验
将活性化合物在DMSO中单独配制成浓度为10000ppm的储备溶液。氟啶胺和氧唑菌以市售配制剂使用并用水稀释得到10000ppm的储备溶液。
将测量的参数与不含活性化合物的对照方案的生长以及不含真菌和活性化合物的空白值比较,以确定病原体在各活性化合物中的相对生长百分数。
应用实施例3-在微滴定板试验中对晚疫病病原体致病疫霉的活性
将储备溶液用移液管移入微滴定板(MTP)中并用基于豌豆浆的含水真菌营养物介质稀释至所述活性化合物浓度。然后加入致病疫霉的含水游动孢子悬浮液。将各板置于温度为18℃的水蒸气饱和室中。在接种后第7天使用吸光光度计于405nm测量MTP。
序号 | 活性化合物 | 浓度[ppm] | 比例 | 观察的活性(%) | 根据Colby计算的活性(%) |
17 | I-B | 12532840.25 | 57352754 | ||
18 | 氧唑菌(A7) | 12532 | 319 | ||
19 | 丙硫菌唑(A19) | 328 | 460 | ||
20 | 亚胺菌(B5) | 1 | 36 | ||
21 | 氟啶胺(D1) | 1 | 0 | ||
22 | I-B+A7 | 125+32 | 4∶1 | 73 | 61 |
23 | I-B+A7 | 32+125 | 1∶4 | 88 | 55 |
24 | I-B+A19 | 32+8 | 4∶1 | 47 | 35 |
25 | I-B+A19 | 8+32 | 1∶4 | 77 | 60 |
26 | I-B+B5 | 4+1 | 4∶1 | 65 | 39 |
27 | I-B+B5 | 0.25+1 | 1∶4 | 53 | 38 |
28 | I-B+D1 | 4+1 | 4∶1 | 92 | 5 |
29 | I-B+D1 | 0.25+1 | 1∶4 | 41 | 5 |
应用实施例4-在微滴定板试验中对灰霉病病原体灰葡萄孢的活性
将储备溶液用移液管移入微滴定板(MTP)中并用基于麦芽的含水真菌营养物介质稀释至所述活性化合物浓度。然后加入灰葡萄孢的含水孢子悬浮液。将各板置于温度为18℃的水蒸气饱和室中。在接种后第7天使用吸光光度计于405nm测量MTP。
序号 | 活性化合物 | 浓度[ppm] | 比例 | 观察的活性(%) | 根据Colby计算的活性(%) |
30 | I-B | 410.25 | 67402 | ||
31 | 氧唑菌(A7) | 1 | 2 | ||
32 | 氰霜唑(A30) | 1 | 00 | ||
33 | 唑菌胺酯(B8) | 0.25 | 20 | ||
34 | 代森锰锌(E1) | 4 | 9 | ||
35 | I-B+A7 | 1+1 | 1∶1 | 67 | 41 |
36 | I-B+A30 | 1+0.25 | 4∶1 | 58 | 40 |
37 | I-B+A30 | 1+4 | 1∶4 | 100 | 40 |
38 | I-B+B8 | 0.25+0.25 | 1∶1 | 55 | 22 |
39 | I-B+E1 | 4+4 | 1∶1 | 97 | 70 |
试验结果表明,由于协同增效作用,本发明混合物与使用Colby公式预测的相比显著更具活性。
Claims (11)
1.一种防治植物病原性有害真菌的杀真菌混合物,该混合物以协同增效有效量包含如下两种活性组分:
1)式I的氨基甲酸酯肟醚:
其中X为N或CH,
和
2)至少一种选自下组的活性化合物II:
A)唑类,例如双苯三唑醇、糠菌唑、环唑醇、醚唑、烯唑醇、烯菌灵、氧唑菌、喹唑菌酮、腈苯唑、氟硅唑、粉唑醇、己唑醇、酰胺唑、环戊唑醇、环戊唑菌、腈菌唑、戊菌唑、丙环唑、丙硫菌唑、硅氟唑、三唑酮、唑菌醇、戊唑醇、氟醚唑、戊叉唑菌、丙氯灵、稻瘟酯、烯菌灵、氟菌唑、氰霜唑、苯菌灵、多菌灵、涕必灵、麦穗宁、噻唑菌胺、氯唑灵、土菌消,
B)嗜球果伞素类,如腈嘧菌酯、醚菌胺、烯肟菌酯、氟嘧菌酯、亚胺菌、叉氨苯酰胺、肟醚菌胺、啶氧菌酯、唑菌胺酯、肟菌酯;
C)羧酰胺类,如萎锈灵、苯霜灵、啶酰菌胺、环酰菌胺、氟酰胺、呋吡唑灵、丙氧灭绣胺、甲霜灵、精甲霜灵、甲呋酰胺、霜灵、氧化萎锈灵、吡噻菌胺、溴氟唑菌、噻酰菌胺,
3,4-二氯-N-(2-氰基苯基)异噻唑-5-甲酰胺、烯酰吗啉、氟吗啉,氟联苯菌、氟吡菌胺、苯酰菌胺,
氯环丙酰胺、双氯氰菌胺、双炔酰菌胺,
N-(2-{4-[3-(4-氯苯基)丙-2-炔基氧基]-3-甲氧基苯基}乙基)-2-甲磺酰氨基-3-甲基丁酰胺、N-(2-{4-[3-(4-氯苯基)丙-2-炔基氧基]-3-甲氧基苯基}乙基)-2-乙磺酰氨基-3-甲基丁酰胺,
式III的酰胺:
其中各变量和指数如下所定义:
R1和R2相互独立地为氢、卤素、C1-C6烷基或C1-C6卤代烷基、氰基、硝基、甲氧基或三氟甲氧基,条件是R1和R2不同时为氢,和R3为CF3或CHF2;
D)杂环化合物,如氟啶胺、啶斑肟、磺嘧菌灵、环丙嘧啶、异嘧菌醇、嘧菌腙、嘧菌胺、氟苯嘧啶醇、二甲嘧菌胺,
嗪氨灵,
拌种咯、氟菌,
4-十二烷基-2,6-二甲基吗啉、吗菌灵、丁苯吗啉、克啉菌,
苯锈啶,
异丙定、杀菌利、烯菌酮,
唑酮菌、咪唑菌酮、异噻菌酮、噻菌灵,
5-氯-7-(4-甲基哌啶-1-基)-6-(2,4,6-三氟苯基)[1,2,4]三唑并[1,5-a]嘧啶,敌菌灵、哒菌清、咯喹酮、丙氧喹啉、三环唑,
2-丁氧基-6-碘-3-丙基苯并吡喃-4-酮,
噻二唑素、敌菌丹、克菌丹、棉隆、灭菌丹、氰菌胺、喹氧灵,或
N,N-二甲基-3-(3-溴-6-氟-2-甲基吲哚-1-磺酰基)[1,2,4]三唑-1-磺酰胺;
E)氨基甲酸盐类,如代森锰锌、代森锰、威百亩、代森联、福美铁、甲基代森锌、福美双、代森锌、福美锌,
乙霉威、异丙菌胺、苯噻菌胺、百维灵,
3-(4-氯苯基)-3-(2-异丙氧基羰基氨基-3-甲基丁酰氨基)丙酸甲酯,
F)选自如下的其他杀真菌剂:
胍类:多果定、双胍辛醋酸盐、双胍盐;
抗菌素类:春雷素、链霉素、多氧霉素、井冈霉素;
硝基苯基衍生物:乐杀螨、敌螨普、敌螨通,
含硫的杂环基化合物:二噻农、稻瘟灵,
有机金属化合物类:三苯锡基盐,如薯瘟锡,
有机磷化合物:克瘟散、异稻瘟净、藻菌磷、乙膦铝、亚磷酸及其盐、定菌磷、甲基立枯磷;
有机氯化合物:百菌清、抑菌灵、磺菌胺、六氯苯、四氯苯酞、戊菌隆、五氯硝基苯、甲基托布津、对甲抑菌灵,
无机活性化合物:波尔多液、醋酸铜、氢氧化铜、王铜、碱式硫酸铜、硫,
其他:环氟菌胺、清菌脲、甲菌定、乙菌定、呋氨丙灵、苯菌酮和螺茂胺。
3.根据权利要求1的杀真菌混合物,包含化合物I-B作为式I的氨基甲酸酯肟醚:
4.根据权利要求1-3中任一项的杀真菌混合物,以100∶1-1∶100的重量比包含式I化合物和式II化合物。
5.一种组合物,包含液体或固体载体和根据权利要求1-4中任一项的混合物。
6.一种防治植物病原性有害真菌的方法,包括用有效量的根据权利要求1的化合物I和化合物II处理真菌、其栖息地或需要防止真菌侵袭的种子、土壤或植物。
7.根据权利要求6的方法,其中同时,即联合或分开施用或依次施用根据权利要求1的化合物I和II。
8.根据权利要求6或7的方法,其中以5-2000g/ha的量施用根据权利要求1的化合物I和II或根据权利要求1-3中任一项的混合物。
9.根据权利要求6或7的方法,其中以1-1000g/100kg种子的量施用根据权利要求1的化合物I和II或根据权利要求1-4中任一项的混合物。
10.种子,以1-1000g/100kg的量包含根据权利要求1-4中任一项的混合物。
11.根据权利要求1的化合物I和II在制备适于防治有害真菌的组合物中的用途。
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE102004063382.7 | 2004-12-23 | ||
DE102004063382 | 2004-12-23 | ||
PCT/EP2005/013816 WO2006069716A1 (de) | 2004-12-23 | 2005-12-21 | Fungizide mischungen |
Publications (2)
Publication Number | Publication Date |
---|---|
CN101087530A true CN101087530A (zh) | 2007-12-12 |
CN101087530B CN101087530B (zh) | 2010-10-13 |
Family
ID=36168395
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN2005800447391A Expired - Fee Related CN101087530B (zh) | 2004-12-23 | 2005-12-21 | 杀真菌混合物 |
Country Status (18)
Country | Link |
---|---|
US (1) | US20080153701A1 (zh) |
EP (1) | EP1830653A1 (zh) |
JP (1) | JP2008525354A (zh) |
KR (1) | KR20070089868A (zh) |
CN (1) | CN101087530B (zh) |
AP (1) | AP2007004080A0 (zh) |
AR (1) | AR052184A1 (zh) |
AU (1) | AU2005321582A1 (zh) |
BR (1) | BRPI0519699A2 (zh) |
CA (1) | CA2590368A1 (zh) |
CR (1) | CR9196A (zh) |
EA (1) | EA011513B1 (zh) |
IL (1) | IL183675A0 (zh) |
MA (1) | MA29158B1 (zh) |
MX (1) | MX2007006799A (zh) |
TW (1) | TW200637494A (zh) |
WO (1) | WO2006069716A1 (zh) |
ZA (1) | ZA200706006B (zh) |
Cited By (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102919254A (zh) * | 2010-12-08 | 2013-02-13 | 陕西美邦农药有限公司 | 一种含十三吗啉的杀菌组合物 |
CN103329916A (zh) * | 2013-07-25 | 2013-10-02 | 联保作物科技有限公司 | 一种杀菌组合物及其制剂 |
CN103561577A (zh) * | 2011-06-01 | 2014-02-05 | 住友化学株式会社 | 害虫防治组合物和用于防治害虫的方法 |
CN104982451A (zh) * | 2015-06-03 | 2015-10-21 | 东莞市瑞德丰生物科技有限公司 | 含有吡菌苯威的杀菌组合物 |
CN104996450A (zh) * | 2015-06-03 | 2015-10-28 | 东莞市瑞德丰生物科技有限公司 | 含有吡菌苯威的杀菌组合物 |
CN105028438A (zh) * | 2015-06-03 | 2015-11-11 | 东莞市瑞德丰生物科技有限公司 | 含有吡菌苯威的杀菌组合物 |
CN105309454A (zh) * | 2015-06-02 | 2016-02-10 | 深圳诺普信农化股份有限公司 | 一种以吡菌苯威为主要成分的杀菌组合物 |
CN105309455A (zh) * | 2015-06-02 | 2016-02-10 | 深圳诺普信农化股份有限公司 | 一种以吡菌苯威为主要成分的杀菌组合物 |
CN106577704A (zh) * | 2016-12-08 | 2017-04-26 | 深圳诺普信农化股份有限公司 | 含有吡菌苯威的杀菌组合物 |
CN106665621A (zh) * | 2016-12-08 | 2017-05-17 | 深圳诺普信农化股份有限公司 | 杀菌组合物 |
CN108157382A (zh) * | 2016-12-08 | 2018-06-15 | 深圳诺普信农化股份有限公司 | 一种吡菌苯威杀菌组合物及其应用 |
CN108174860A (zh) * | 2016-12-08 | 2018-06-19 | 深圳诺普信农化股份有限公司 | 含有吡菌苯威的杀菌组合物 |
CN108184877A (zh) * | 2016-12-08 | 2018-06-22 | 深圳诺普信农化股份有限公司 | 一种吡菌苯威杀菌组合物 |
Families Citing this family (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB0508993D0 (en) | 2005-05-03 | 2005-06-08 | Syngenta Participations Ag | Pesticidal compositions |
BRPI0612726A2 (pt) * | 2005-07-05 | 2016-11-29 | Basf Aktiengesellschaff | misturas fungicidas para combater fungos nocivos fitopatogênicos, agente fungicida, processo para combater fungos nocivos fitopatogênicos, semente, e, uso de compostos |
RS53673B1 (en) * | 2005-08-05 | 2015-04-30 | Basf Se | FUNGICID MIXTURES CONTAINING SUBSTITUTED ANILIDES 1-METHYL-PIRAZOL-4-IL CARBOXYLIC ACIDS |
ATE555657T1 (de) * | 2005-09-29 | 2012-05-15 | Syngenta Participations Ag | Fungizidzusammensetzungen |
CN102511490B (zh) * | 2007-10-09 | 2013-06-19 | 中国中化股份有限公司 | 一种杀真菌组合物 |
US8268755B2 (en) | 2007-12-11 | 2012-09-18 | Nippon Soda Co., Ltd. | Oxime ether derivative and fungicide for agricultural and horticultural use |
DK2649880T3 (en) | 2008-03-24 | 2017-07-31 | Nippon Soda Co | Plant Disease Mediterranean |
JP2012162460A (ja) * | 2009-05-27 | 2012-08-30 | Nippon Soda Co Ltd | 含窒素ヘテロアリール誘導体および農園芸用殺菌剤 |
JP2011042664A (ja) * | 2010-10-08 | 2011-03-03 | Kumiai Chemical Industry Co Ltd | 農園芸用殺菌剤組成物 |
CN103563921B (zh) * | 2012-08-04 | 2015-11-18 | 南京华洲药业有限公司 | 一种含噻呋酰胺和粉唑醇的杀菌组合物及其应用 |
CN103918686B (zh) * | 2014-05-07 | 2016-09-07 | 陕西上格之路生物科学有限公司 | 一种含有甲基硫菌灵的可分散油悬浮剂 |
RU2623264C1 (ru) * | 2016-07-07 | 2017-06-23 | Михаил Михайлович Акулин | Инсектофунгицидная пиротехническая композиция |
JP2023538949A (ja) * | 2020-08-28 | 2023-09-12 | ガシャーブラム・バイオ・インコーポレイテッド | ヘテロ環glp-1アゴニスト |
Family Cites Families (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE4326860C2 (de) * | 1993-08-06 | 2002-06-06 | Schering Ag | Fungizides Mittel mit synergistischer Wirkung |
UA73307C2 (uk) * | 1999-08-05 | 2005-07-15 | Куміаі Кемікал Індастрі Ко., Лтд. | Похідна карбамату і фунгіцид сільськогосподарського/садівницького призначення |
JP4246996B2 (ja) * | 2001-02-02 | 2009-04-02 | クミアイ化学工業株式会社 | イミノオキシメチルピリジン化合物及び農園芸用殺菌剤 |
DE10141617A1 (de) * | 2001-08-24 | 2003-03-06 | Bayer Cropscience Ag | Fungizide Wirkstoffkombinationen |
DE10141618A1 (de) * | 2001-08-24 | 2003-03-06 | Bayer Cropscience Ag | Fungizide Wirkstoffkombinationen |
JP4112915B2 (ja) * | 2002-07-02 | 2008-07-02 | クミアイ化学工業株式会社 | 農園芸用殺菌剤組成物及びカーバメート化合物の殺菌効力増強剤 |
-
2005
- 2005-12-21 EP EP05819380A patent/EP1830653A1/de active Pending
- 2005-12-21 KR KR1020077016620A patent/KR20070089868A/ko not_active Application Discontinuation
- 2005-12-21 WO PCT/EP2005/013816 patent/WO2006069716A1/de active Application Filing
- 2005-12-21 AU AU2005321582A patent/AU2005321582A1/en not_active Abandoned
- 2005-12-21 CN CN2005800447391A patent/CN101087530B/zh not_active Expired - Fee Related
- 2005-12-21 CA CA002590368A patent/CA2590368A1/en not_active Abandoned
- 2005-12-21 US US11/793,795 patent/US20080153701A1/en not_active Abandoned
- 2005-12-21 AP AP2007004080A patent/AP2007004080A0/xx unknown
- 2005-12-21 MX MX2007006799A patent/MX2007006799A/es not_active Application Discontinuation
- 2005-12-21 JP JP2007547348A patent/JP2008525354A/ja not_active Withdrawn
- 2005-12-21 BR BRPI0519699-0A patent/BRPI0519699A2/pt not_active IP Right Cessation
- 2005-12-21 EA EA200701223A patent/EA011513B1/ru not_active IP Right Cessation
- 2005-12-22 AR ARP050105514A patent/AR052184A1/es unknown
- 2005-12-23 TW TW094146383A patent/TW200637494A/zh unknown
-
2007
- 2007-06-05 IL IL183675A patent/IL183675A0/en unknown
- 2007-06-19 CR CR9196A patent/CR9196A/es not_active Application Discontinuation
- 2007-07-20 ZA ZA200706006A patent/ZA200706006B/xx unknown
- 2007-07-20 MA MA30085A patent/MA29158B1/fr unknown
Cited By (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102919254A (zh) * | 2010-12-08 | 2013-02-13 | 陕西美邦农药有限公司 | 一种含十三吗啉的杀菌组合物 |
CN103561577A (zh) * | 2011-06-01 | 2014-02-05 | 住友化学株式会社 | 害虫防治组合物和用于防治害虫的方法 |
CN103561577B (zh) * | 2011-06-01 | 2015-10-14 | 住友化学株式会社 | 害虫防治组合物和用于防治害虫的方法 |
CN103329916A (zh) * | 2013-07-25 | 2013-10-02 | 联保作物科技有限公司 | 一种杀菌组合物及其制剂 |
CN103329916B (zh) * | 2013-07-25 | 2014-06-11 | 联保作物科技有限公司 | 一种杀菌组合物及其制剂 |
CN105309455A (zh) * | 2015-06-02 | 2016-02-10 | 深圳诺普信农化股份有限公司 | 一种以吡菌苯威为主要成分的杀菌组合物 |
CN105309454A (zh) * | 2015-06-02 | 2016-02-10 | 深圳诺普信农化股份有限公司 | 一种以吡菌苯威为主要成分的杀菌组合物 |
CN104996450A (zh) * | 2015-06-03 | 2015-10-28 | 东莞市瑞德丰生物科技有限公司 | 含有吡菌苯威的杀菌组合物 |
CN105028438A (zh) * | 2015-06-03 | 2015-11-11 | 东莞市瑞德丰生物科技有限公司 | 含有吡菌苯威的杀菌组合物 |
CN104982451A (zh) * | 2015-06-03 | 2015-10-21 | 东莞市瑞德丰生物科技有限公司 | 含有吡菌苯威的杀菌组合物 |
CN106577704A (zh) * | 2016-12-08 | 2017-04-26 | 深圳诺普信农化股份有限公司 | 含有吡菌苯威的杀菌组合物 |
CN106665621A (zh) * | 2016-12-08 | 2017-05-17 | 深圳诺普信农化股份有限公司 | 杀菌组合物 |
CN108157382A (zh) * | 2016-12-08 | 2018-06-15 | 深圳诺普信农化股份有限公司 | 一种吡菌苯威杀菌组合物及其应用 |
CN108174860A (zh) * | 2016-12-08 | 2018-06-19 | 深圳诺普信农化股份有限公司 | 含有吡菌苯威的杀菌组合物 |
CN108184877A (zh) * | 2016-12-08 | 2018-06-22 | 深圳诺普信农化股份有限公司 | 一种吡菌苯威杀菌组合物 |
Also Published As
Publication number | Publication date |
---|---|
EP1830653A1 (de) | 2007-09-12 |
EA200701223A1 (ru) | 2007-12-28 |
TW200637494A (en) | 2006-11-01 |
CN101087530B (zh) | 2010-10-13 |
CR9196A (es) | 2007-10-04 |
IL183675A0 (en) | 2007-09-20 |
AR052184A1 (es) | 2007-03-07 |
US20080153701A1 (en) | 2008-06-26 |
MX2007006799A (es) | 2007-07-20 |
ZA200706006B (en) | 2009-08-26 |
JP2008525354A (ja) | 2008-07-17 |
EA011513B1 (ru) | 2009-04-28 |
MA29158B1 (fr) | 2008-01-02 |
AU2005321582A1 (en) | 2006-07-06 |
WO2006069716A1 (de) | 2006-07-06 |
AP2007004080A0 (en) | 2007-08-31 |
KR20070089868A (ko) | 2007-09-03 |
BRPI0519699A2 (pt) | 2009-07-14 |
CA2590368A1 (en) | 2006-07-06 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN101087530B (zh) | 杀真菌混合物 | |
CN101087529B (zh) | 杀真菌混合物 | |
CN105165883B (zh) | 基于唑并嘧啶基胺的杀真菌混合物 | |
CN101257798A (zh) | 包含取代的1-甲基吡唑-4-基甲酰苯胺的杀真菌混合物 | |
CN104604873A (zh) | 包含取代的1-甲基吡唑-4-基甲酰苯胺的杀真菌混合物 | |
CN1937920A (zh) | 三元杀真菌混合物 | |
CN101087525A (zh) | 含有烯肟菌酯和至少一种选自唑类的活性物质的杀真菌混合物 | |
CN100591207C (zh) | 提高噻唑菌胺的有效性的方法 | |
JP2009502747A (ja) | 1−メチル−ピラゾール−4−イルカルボキシアニリド類に基づく殺菌性混合物 | |
CN101267735A (zh) | 包含n-[2-(卤代烷(烯基)氧基)苯基]甲酰胺的杀真菌混合物 | |
US20090233795A1 (en) | Fungicidal Mixtres Based On 3-Monosubstituted N-Bipenyl-Pyrazolecarboxamides | |
EP1898704A1 (de) | Fungizide mischungen auf der basis von 2,5-disubstituierten pyrazolcarbonsäurebiphenylamiden | |
CN101262764A (zh) | 基于1-甲基吡唑-4-基甲酰苯胺的杀真菌混合物 | |
CN101212902A (zh) | 基于3,5-二取代的吡唑甲酸联苯基酰胺的杀真菌混合物 | |
WO2007003564A1 (de) | Fungizide mischungen auf der basis von 3,5-disubstituierten pyrazolcarbonsäurebiphenylamiden | |
EP1813151A1 (de) | Fungizide Mischungen auf der Basis von 1-Methyl-pyrazol-4-yl-carbonsäureaniliden | |
CN101217873A (zh) | 由1-甲基吡唑-4-基甲酰苯胺制成的杀真菌混合物 | |
CN1972594A (zh) | 基于三唑并嘧啶衍生物的杀真菌混合物 | |
CN101212901A (zh) | 基于2,5-二取代的吡唑甲酸联苯基酰胺的杀真菌混合物 | |
CN101212900A (zh) | 基于2,4-二取代的吡唑甲酸联苯基酰胺的杀真菌混合物 | |
CN101247723A (zh) | 基于3-单取代的吡唑甲酸联苯基酰胺的杀真菌混合物 | |
CN101511182A (zh) | 防治真菌害虫的方法 | |
JP2009526745A (ja) | 2,4−二置換n−ビフェニルピラゾールカルボキシアミドに基づく殺菌混合物 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
C06 | Publication | ||
PB01 | Publication | ||
C10 | Entry into substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
C14 | Grant of patent or utility model | ||
GR01 | Patent grant | ||
C17 | Cessation of patent right | ||
CF01 | Termination of patent right due to non-payment of annual fee |
Granted publication date: 20101013 Termination date: 20101221 |