CN1026548C - 植物保护组合物 - Google Patents
植物保护组合物 Download PDFInfo
- Publication number
- CN1026548C CN1026548C CN88106116A CN88106116A CN1026548C CN 1026548 C CN1026548 C CN 1026548C CN 88106116 A CN88106116 A CN 88106116A CN 88106116 A CN88106116 A CN 88106116A CN 1026548 C CN1026548 C CN 1026548C
- Authority
- CN
- China
- Prior art keywords
- composition
- water
- weight
- plant
- compound
- 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.)
- Expired - Fee Related
Links
- 239000000203 mixture Substances 0.000 title claims description 83
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 claims abstract description 66
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 62
- 239000002904 solvent Substances 0.000 claims abstract description 34
- 239000000725 suspension Substances 0.000 claims abstract description 31
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 claims abstract description 20
- 239000002245 particle Substances 0.000 claims abstract description 19
- XPFVYQJUAUNWIW-UHFFFAOYSA-N furfuryl alcohol Chemical compound OCC1=CC=CO1 XPFVYQJUAUNWIW-UHFFFAOYSA-N 0.000 claims abstract description 17
- 239000000654 additive Substances 0.000 claims abstract description 15
- 239000004094 surface-active agent Substances 0.000 claims abstract description 14
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 claims abstract description 12
- 230000000996 additive effect Effects 0.000 claims abstract description 12
- 239000003337 fertilizer Substances 0.000 claims abstract description 12
- 229920002521 macromolecule Polymers 0.000 claims abstract 4
- 239000000243 solution Substances 0.000 claims description 47
- 238000002360 preparation method Methods 0.000 claims description 37
- DUEPRVBVGDRKAG-UHFFFAOYSA-N carbofuran Chemical compound CNC(=O)OC1=CC=CC2=C1OC(C)(C)C2 DUEPRVBVGDRKAG-UHFFFAOYSA-N 0.000 claims description 34
- HYBBIBNJHNGZAN-UHFFFAOYSA-N furfural Chemical compound O=CC1=CC=CO1 HYBBIBNJHNGZAN-UHFFFAOYSA-N 0.000 claims description 34
- 150000001875 compounds Chemical class 0.000 claims description 18
- 239000007788 liquid Substances 0.000 claims description 16
- 230000002633 protecting effect Effects 0.000 claims description 14
- -1 Isopropyl 3-chlorphenyl carbamate Chemical compound 0.000 claims description 9
- 229910019142 PO4 Inorganic materials 0.000 claims description 8
- 239000010452 phosphate Substances 0.000 claims description 8
- DLFVBJFMPXGRIB-UHFFFAOYSA-N Acetamide Chemical compound CC(N)=O DLFVBJFMPXGRIB-UHFFFAOYSA-N 0.000 claims description 6
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims description 6
- 239000004202 carbamide Substances 0.000 claims description 6
- ZHNUHDYFZUAESO-UHFFFAOYSA-N Formamide Chemical compound NC=O ZHNUHDYFZUAESO-UHFFFAOYSA-N 0.000 claims description 4
- 150000001450 anions Chemical class 0.000 claims description 4
- SCWKRWCUMCMVPW-UHFFFAOYSA-N phenyl n-methylcarbamate Chemical compound CNC(=O)OC1=CC=CC=C1 SCWKRWCUMCMVPW-UHFFFAOYSA-N 0.000 claims description 4
- 150000003013 phosphoric acid derivatives Chemical class 0.000 claims description 4
- CVXBEEMKQHEXEN-UHFFFAOYSA-N carbaryl Chemical compound C1=CC=C2C(OC(=O)NC)=CC=CC2=C1 CVXBEEMKQHEXEN-UHFFFAOYSA-N 0.000 claims description 3
- LHTOXQCYXYXXEZ-UHFFFAOYSA-N (3-pentan-2-ylphenyl) n-methylcarbamate Chemical compound CCCC(C)C1=CC=CC(OC(=O)NC)=C1 LHTOXQCYXYXXEZ-UHFFFAOYSA-N 0.000 claims description 2
- LUBJCRLGQSPQNN-UHFFFAOYSA-N 1-Phenylurea Chemical compound NC(=O)NC1=CC=CC=C1 LUBJCRLGQSPQNN-UHFFFAOYSA-N 0.000 claims description 2
- UENGBOCGGKLVJJ-UHFFFAOYSA-N 2-chloro-1-(2,4-difluorophenyl)ethanone Chemical compound FC1=CC=C(C(=O)CCl)C(F)=C1 UENGBOCGGKLVJJ-UHFFFAOYSA-N 0.000 claims description 2
- MHIXOQXRXDCMMA-UHFFFAOYSA-N 2-methoxyiminopropanediamide Chemical compound CON=C(C(N)=O)C(N)=O MHIXOQXRXDCMMA-UHFFFAOYSA-N 0.000 claims description 2
- LIGJCMDIPLLARI-UHFFFAOYSA-N CCN(CC)C1(C=C(C=C(C1N)[N+](=O)[O-])C(F)(F)F)[N+](=O)[O-] Chemical compound CCN(CC)C1(C=C(C=C(C1N)[N+](=O)[O-])C(F)(F)F)[N+](=O)[O-] LIGJCMDIPLLARI-UHFFFAOYSA-N 0.000 claims description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 2
- UMKANAFDOQQUKE-UHFFFAOYSA-N Nitralin Chemical compound CCCN(CCC)C1=C([N+]([O-])=O)C=C(S(C)(=O)=O)C=C1[N+]([O-])=O UMKANAFDOQQUKE-UHFFFAOYSA-N 0.000 claims description 2
- LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical compound OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 claims description 2
- 239000007864 aqueous solution Substances 0.000 claims description 2
- 239000007900 aqueous suspension Substances 0.000 claims description 2
- GTCAXTIRRLKXRU-UHFFFAOYSA-N carbamic acid methyl ester Natural products COC(N)=O GTCAXTIRRLKXRU-UHFFFAOYSA-N 0.000 claims description 2
- 229960005286 carbaryl Drugs 0.000 claims description 2
- 125000002603 chloroethyl group Chemical group [H]C([*])([H])C([H])([H])Cl 0.000 claims description 2
- 125000004122 cyclic group Chemical group 0.000 claims description 2
- 125000000623 heterocyclic group Chemical group 0.000 claims description 2
- QBSJMKIUCUGGNG-UHFFFAOYSA-N isoprocarb Chemical compound CNC(=O)OC1=CC=CC=C1C(C)C QBSJMKIUCUGGNG-UHFFFAOYSA-N 0.000 claims description 2
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 2
- KXDHJXZQYSOELW-UHFFFAOYSA-M Carbamate Chemical compound NC([O-])=O KXDHJXZQYSOELW-UHFFFAOYSA-M 0.000 claims 2
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 claims 2
- MHKBMNACOMRIAW-UHFFFAOYSA-N 2,3-dinitrophenol Chemical compound OC1=CC=CC([N+]([O-])=O)=C1[N+]([O-])=O MHKBMNACOMRIAW-UHFFFAOYSA-N 0.000 claims 1
- 150000002391 heterocyclic compounds Chemical class 0.000 claims 1
- 125000000129 anionic group Chemical group 0.000 abstract 2
- 239000004615 ingredient Substances 0.000 abstract 2
- 230000001502 supplementing effect Effects 0.000 abstract 1
- 239000002689 soil Substances 0.000 description 25
- 238000004659 sterilization and disinfection Methods 0.000 description 18
- 241000196324 Embryophyta Species 0.000 description 16
- 239000013078 crystal Substances 0.000 description 14
- 239000002002 slurry Substances 0.000 description 13
- 238000005507 spraying Methods 0.000 description 10
- 238000007046 ethoxylation reaction Methods 0.000 description 9
- 230000000694 effects Effects 0.000 description 8
- 235000013339 cereals Nutrition 0.000 description 7
- 235000014113 dietary fatty acids Nutrition 0.000 description 7
- 239000000194 fatty acid Substances 0.000 description 7
- 229930195729 fatty acid Natural products 0.000 description 7
- 150000004665 fatty acids Chemical class 0.000 description 7
- 238000000034 method Methods 0.000 description 6
- 239000012071 phase Substances 0.000 description 6
- 238000003756 stirring Methods 0.000 description 6
- 150000008055 alkyl aryl sulfonates Chemical group 0.000 description 5
- 229920000642 polymer Polymers 0.000 description 5
- 239000000126 substance Substances 0.000 description 5
- 241000607479 Yersinia pestis Species 0.000 description 4
- 240000008042 Zea mays Species 0.000 description 4
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 4
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 4
- 235000005822 corn Nutrition 0.000 description 4
- 239000000839 emulsion Substances 0.000 description 4
- 239000004009 herbicide Substances 0.000 description 4
- 241000238631 Hexapoda Species 0.000 description 3
- 239000005867 Iprodione Substances 0.000 description 3
- 239000005581 Metobromuron Substances 0.000 description 3
- WLFDQEVORAMCIM-UHFFFAOYSA-N Metobromuron Chemical compound CON(C)C(=O)NC1=CC=C(Br)C=C1 WLFDQEVORAMCIM-UHFFFAOYSA-N 0.000 description 3
- 241000269799 Perca fluviatilis Species 0.000 description 3
- 231100000674 Phytotoxicity Toxicity 0.000 description 3
- 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 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 239000004476 plant protection product Substances 0.000 description 3
- 238000011160 research Methods 0.000 description 3
- 239000007790 solid phase Substances 0.000 description 3
- 239000011877 solvent mixture Substances 0.000 description 3
- 238000009331 sowing Methods 0.000 description 3
- ZSDSQXJSNMTJDA-UHFFFAOYSA-N trifluralin Chemical compound CCCN(CCC)C1=C([N+]([O-])=O)C=C(C(F)(F)F)C=C1[N+]([O-])=O ZSDSQXJSNMTJDA-UHFFFAOYSA-N 0.000 description 3
- 241001136249 Agriotes lineatus Species 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- 241000209140 Triticum Species 0.000 description 2
- 235000021307 Triticum Nutrition 0.000 description 2
- 230000000857 drug effect Effects 0.000 description 2
- 239000004495 emulsifiable concentrate Substances 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 239000002360 explosive Substances 0.000 description 2
- 239000012530 fluid Substances 0.000 description 2
- 230000002363 herbicidal effect Effects 0.000 description 2
- 230000002045 lasting effect Effects 0.000 description 2
- 239000012457 nonaqueous media Substances 0.000 description 2
- 239000003921 oil Substances 0.000 description 2
- YZHUMGUJCQRKBT-UHFFFAOYSA-M sodium chlorate Chemical compound [Na+].[O-]Cl(=O)=O YZHUMGUJCQRKBT-UHFFFAOYSA-M 0.000 description 2
- 239000000375 suspending agent Substances 0.000 description 2
- 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 description 1
- XUNYDVLIZWUPAW-UHFFFAOYSA-N (4-chlorophenyl) n-(4-methylphenyl)sulfonylcarbamate Chemical compound C1=CC(C)=CC=C1S(=O)(=O)NC(=O)OC1=CC=C(Cl)C=C1 XUNYDVLIZWUPAW-UHFFFAOYSA-N 0.000 description 1
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 1
- POAOYUHQDCAZBD-UHFFFAOYSA-N 2-butoxyethanol Chemical compound CCCCOCCO POAOYUHQDCAZBD-UHFFFAOYSA-N 0.000 description 1
- DUIOKRXOKLLURE-UHFFFAOYSA-N 2-octylphenol Chemical compound CCCCCCCCC1=CC=CC=C1O DUIOKRXOKLLURE-UHFFFAOYSA-N 0.000 description 1
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 1
- XJFIKRXIJXAJGH-UHFFFAOYSA-N 5-chloro-1,3-dihydroimidazo[4,5-b]pyridin-2-one Chemical group ClC1=CC=C2NC(=O)NC2=N1 XJFIKRXIJXAJGH-UHFFFAOYSA-N 0.000 description 1
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 1
- 241000059559 Agriotes sordidus Species 0.000 description 1
- NYQDCVLCJXRDSK-UHFFFAOYSA-N Bromofos Chemical compound COP(=S)(OC)OC1=CC(Cl)=C(Br)C=C1Cl NYQDCVLCJXRDSK-UHFFFAOYSA-N 0.000 description 1
- 239000005647 Chlorpropham Substances 0.000 description 1
- 239000005945 Chlorpyrifos-methyl Substances 0.000 description 1
- 206010010071 Coma Diseases 0.000 description 1
- 239000005756 Cymoxanil Substances 0.000 description 1
- 241001414890 Delia Species 0.000 description 1
- MUMQYXACQUZOFP-UHFFFAOYSA-N Dialifor Chemical compound C1=CC=C2C(=O)N(C(CCl)SP(=S)(OCC)OCC)C(=O)C2=C1 MUMQYXACQUZOFP-UHFFFAOYSA-N 0.000 description 1
- URDNHJIVMYZFRT-UHFFFAOYSA-N Diclobutrazol Chemical compound C1=NC=NN1C(C(O)C(C)(C)C)CC1=CC=C(Cl)C=C1Cl URDNHJIVMYZFRT-UHFFFAOYSA-N 0.000 description 1
- 239000005893 Diflubenzuron Substances 0.000 description 1
- IIPZYDQGBIWLBU-UHFFFAOYSA-N Dinoterb Chemical compound CC(C)(C)C1=CC([N+]([O-])=O)=CC([N+]([O-])=O)=C1O IIPZYDQGBIWLBU-UHFFFAOYSA-N 0.000 description 1
- DNXHEGUUPJUMQT-CBZIJGRNSA-N Estrone Chemical compound OC1=CC=C2[C@H]3CC[C@](C)(C(CC4)=O)[C@@H]4[C@@H]3CCC2=C1 DNXHEGUUPJUMQT-CBZIJGRNSA-N 0.000 description 1
- 241000087799 Koma Species 0.000 description 1
- RRVIAQKBTUQODI-UHFFFAOYSA-N Methabenzthiazuron Chemical compound C1=CC=C2SC(N(C)C(=O)NC)=NC2=C1 RRVIAQKBTUQODI-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
- 239000005642 Oleic acid Substances 0.000 description 1
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- DTAPQAJKAFRNJB-UHFFFAOYSA-N Promecarb Chemical compound CNC(=O)OC1=CC(C)=CC(C(C)C)=C1 DTAPQAJKAFRNJB-UHFFFAOYSA-N 0.000 description 1
- 208000032825 Ring chromosome 2 syndrome Diseases 0.000 description 1
- GNVMUORYQLCPJZ-UHFFFAOYSA-M Thiocarbamate Chemical compound NC([S-])=O GNVMUORYQLCPJZ-UHFFFAOYSA-M 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 150000003869 acetamides Chemical class 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 239000003945 anionic surfactant Substances 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 230000000975 bioactive effect Effects 0.000 description 1
- 230000004071 biological effect Effects 0.000 description 1
- 159000000007 calcium salts Chemical class 0.000 description 1
- 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 1
- 150000004657 carbamic acid derivatives Chemical class 0.000 description 1
- 239000004568 cement Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- CWJSHJJYOPWUGX-UHFFFAOYSA-N chlorpropham Chemical compound CC(C)OC(=O)NC1=CC=CC(Cl)=C1 CWJSHJJYOPWUGX-UHFFFAOYSA-N 0.000 description 1
- 239000000084 colloidal system Substances 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 229940019503 diflubenzuron Drugs 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- YRIUSKIDOIARQF-UHFFFAOYSA-N dodecyl benzenesulfonate Chemical compound CCCCCCCCCCCCOS(=O)(=O)C1=CC=CC=C1 YRIUSKIDOIARQF-UHFFFAOYSA-N 0.000 description 1
- 229940071161 dodecylbenzenesulfonate Drugs 0.000 description 1
- 238000004945 emulsification Methods 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 230000001804 emulsifying effect Effects 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 238000005189 flocculation Methods 0.000 description 1
- 230000016615 flocculation Effects 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 125000004836 hexamethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[*:1] 0.000 description 1
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
- CTAPFRYPJLPFDF-UHFFFAOYSA-N isoxazole Chemical compound C=1C=NOC=1 CTAPFRYPJLPFDF-UHFFFAOYSA-N 0.000 description 1
- 239000007791 liquid phase Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 150000002828 nitro derivatives Chemical class 0.000 description 1
- SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical compound CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- 150000007978 oxazole derivatives Chemical class 0.000 description 1
- 150000004885 piperazines Chemical class 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920000151 polyglycol Polymers 0.000 description 1
- 239000010695 polyglycol Substances 0.000 description 1
- 229920002689 polyvinyl acetate Polymers 0.000 description 1
- 239000011118 polyvinyl acetate Substances 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 1
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 238000000518 rheometry Methods 0.000 description 1
- 239000013049 sediment Substances 0.000 description 1
- 238000004062 sedimentation Methods 0.000 description 1
- 238000007873 sieving Methods 0.000 description 1
- 150000003457 sulfones Chemical class 0.000 description 1
- 229940066771 systemic antihistamines piperazine derivative Drugs 0.000 description 1
- 238000012422 test repetition Methods 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- RYYWUUFWQRZTIU-UHFFFAOYSA-K thiophosphate Chemical compound [O-]P([O-])([O-])=S RYYWUUFWQRZTIU-UHFFFAOYSA-K 0.000 description 1
- 150000003852 triazoles Chemical class 0.000 description 1
- 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 description 1
- 150000003672 ureas Chemical class 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
- A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
- A01N25/02—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests containing liquids as carriers, diluents or solvents
-
- 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
- A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
- A01N25/02—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests containing liquids as carriers, diluents or solvents
- A01N25/04—Dispersions, emulsions, suspoemulsions, suspension concentrates or gels
Landscapes
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Health & Medical Sciences (AREA)
- Toxicology (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Agronomy & Crop Science (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Dispersion Chemistry (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| HU873245A HU207197B (en) | 1987-07-16 | 1987-07-16 | Plant protecting solution and aquous suspension containing water insoluble active component |
| HU3245/87 | 1987-07-16 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN1036124A CN1036124A (zh) | 1989-10-11 |
| CN1026548C true CN1026548C (zh) | 1994-11-16 |
Family
ID=10963292
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN88106116A Expired - Fee Related CN1026548C (zh) | 1987-07-16 | 1988-07-15 | 植物保护组合物 |
Country Status (16)
| Country | Link |
|---|---|
| US (1) | US4943307A (enExample) |
| EP (1) | EP0300691B1 (enExample) |
| JP (1) | JPS6490106A (enExample) |
| KR (1) | KR960009483B1 (enExample) |
| CN (1) | CN1026548C (enExample) |
| AR (1) | AR247065A1 (enExample) |
| AT (1) | ATE72923T1 (enExample) |
| BR (1) | BR8803563A (enExample) |
| DD (1) | DD286097A5 (enExample) |
| DE (1) | DE3868751D1 (enExample) |
| ES (1) | ES2037835T3 (enExample) |
| GR (1) | GR3004781T3 (enExample) |
| HU (1) | HU207197B (enExample) |
| PL (1) | PL161573B1 (enExample) |
| RU (1) | RU1836011C (enExample) |
| WO (1) | WO1989000380A1 (enExample) |
Families Citing this family (24)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5141940A (en) * | 1989-05-26 | 1992-08-25 | Shell Internationale Research Maatshappij B.V. | Fungicidal liquid formulations |
| CA2075920A1 (en) * | 1990-12-18 | 1992-06-19 | Jeffrey L. Jensen | Precipitated flowable concentrate formulations, their preparation and their agricultural uses |
| US5707551A (en) * | 1994-12-22 | 1998-01-13 | Rhone-Poulenc Inc. | Nonaqueous suspension concentrates of highly water-soluble solids |
| US5906962A (en) * | 1994-12-22 | 1999-05-25 | Rhodia Inc. | Non-aqueous suspension concentrates of highly water-soluble solids |
| ZA964248B (en) * | 1995-06-23 | 1997-11-27 | Du Pont | Uniform mixtures of pesticidal granules. |
| JPH10143977A (ja) | 1996-09-10 | 1998-05-29 | Sony Corp | ディスク装置およびそれを用いたビデオカメラ装置 |
| EP1087658B1 (en) * | 1998-06-17 | 2004-01-21 | UNIROYAL CHEMICAL COMPANY, Inc. | Biologically-active microdispersion composition |
| DE19834598A1 (de) * | 1998-07-31 | 2000-02-03 | Hoechst Schering Agrevo Gmbh | Wäßriges Suspensionskonzentrat, enthaltend Thidiazuron und Ethephon |
| US6720352B1 (en) * | 1999-05-10 | 2004-04-13 | Illovo Sugar Ltd | Compositions and process for nematode control |
| GB0126144D0 (en) * | 2001-10-31 | 2002-01-02 | Syngenta Ltd | Pesticidal formulations |
| US6743752B2 (en) | 2003-03-28 | 2004-06-01 | Northern Quinoa Corporation | Method of protecting plants from bacterial diseases |
| US20050261129A1 (en) * | 2003-09-22 | 2005-11-24 | Dutcheshen Joseph M | Method of protecting plants from bacterial and fungal diseases |
| IL160858A (en) * | 2004-03-14 | 2015-09-24 | Adama Makhteshim Ltd | Nano-pesticide pesticide preparation and process for preparation |
| GB0503119D0 (en) * | 2005-02-15 | 2005-03-23 | Ici Plc | Agrochemical formulations |
| CN102365962A (zh) * | 2010-10-28 | 2012-03-07 | 河北省农林科学院昌黎果树研究所 | 一种嫁接促愈剂，其制备方法和应用 |
| US10173935B2 (en) | 2011-12-12 | 2019-01-08 | Rhodia Operations | Solvent systems of N-alkyl thiophosphoric triamides and methods of use in agricultural applications |
| AU2013325242B2 (en) | 2012-10-01 | 2018-08-02 | Gary David Mcknight | Improved liquid formulations of urease inhibitors for fertilizers |
| JP6409000B2 (ja) | 2012-12-20 | 2018-10-17 | ローディア オペレーションズ | 液体ジシアンジアミドおよび／またはアルキルチオリン酸トリアミド組成物ならびに農業用途でのそれらの使用 |
| PE20160854A1 (es) | 2013-11-26 | 2016-09-09 | Andrew Michael Semple | Inhibidores de nitrificacion disenados para fertilizantes a base de estiercol y urea |
| WO2015161195A1 (en) | 2014-04-17 | 2015-10-22 | Mcknight Gary David | Compositions and methods comprising ntrification inhibitors containing a mixture of protic and aprotic solvent systems |
| CN119431081A (zh) | 2014-10-21 | 2025-02-14 | 法国特种经营公司 | 用于双氰胺和/或烷基硫代磷酰三胺的改进的溶剂体系以及在农业应用中的用途 |
| US10435333B2 (en) | 2015-08-17 | 2019-10-08 | Rhodia Operations | High temperature amine-stabilized DCD and/or alkyl thiophosphoric triamide solvent systems and use in agricultural applications |
| US11866383B1 (en) | 2018-04-04 | 2024-01-09 | Synsus Private Label Partners, Llc | Nitrification inhibiting compositions and their use in agricultural applications |
| US11124462B1 (en) | 2018-08-27 | 2021-09-21 | Hocking International Laboratories, LLC | Compositions and their use in agricultural applications |
Family Cites Families (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3474170A (en) * | 1964-01-23 | 1969-10-21 | Fmc Corp | Pesticidal carbamates of dihydrobenzofuranols |
| GB1311792A (en) * | 1970-02-16 | 1973-03-28 | Ici Ltd | Pesticidal compositions |
| GB1453696A (en) * | 1972-10-13 | 1976-10-27 | Rentokil Ltd | Method for the production of solid particles |
| NL178647C (nl) * | 1974-03-08 | 1986-05-01 | Duphar Int Res | Werkwijze ter bereiding van een de plantengroei bevorderende vloeibare samenstelling. |
| SU641950A1 (ru) * | 1977-08-08 | 1979-01-15 | Предприятие П/Я Г-4684 | Эмульгирующий концентрат 2,6динитро-4-трифторметил- -ди-н-пропиланилина - нитран - к |
| IT1110255B (it) * | 1979-02-05 | 1985-12-23 | Montedison Spa | Soluzioni a base di n-feniluree n'-alcossi,n'-alchil sostituite erbiciede stabili a temperature da +54 c a -10 c |
| IT1163687B (it) * | 1979-07-27 | 1987-04-08 | Montedison Spa | Soluzioni e formulazioni di carbammati antiparassitari stabili nel tempo e che resistono a basse ed alte temperature |
| HU181665B (en) * | 1979-11-28 | 1983-10-28 | Chinoin Gyogyszer Es Vegyeszet | Plant protective composition containing carbofurane with increased growth promoting and insecticide effect |
| US4464193A (en) * | 1980-02-19 | 1984-08-07 | Basf Wyandotte Corporation | Anionic biocide emulsions in aqueous solutions of strongly ionizable salts |
| CH630227A5 (de) * | 1980-03-11 | 1982-06-15 | Ci Co Me | Verfahren zur herstellung von desinfektionsformulierungen mit spezifischem wirkungsmechanismus. |
| EP0253374A1 (en) * | 1982-07-07 | 1988-01-20 | Agan Chemical Manufacturers Ltd. | A method for combatting blackgrass in cereal crops and compositions therefor |
| HU191184B (en) * | 1982-07-09 | 1987-01-28 | Chinoin Gyogyszer Es Vegyeszeti Termekek Gyara Rt,Hu | Stabilized herbicide suspension |
| GB8308749D0 (en) * | 1983-03-30 | 1983-05-11 | Dow Chemical Co | Emulsifiable concentrate formulations of pesticides |
| US4664093A (en) * | 1985-01-17 | 1987-05-12 | John Nunemaker | Arrow rest assembly for an archery bow |
-
1987
- 1987-07-16 HU HU873245A patent/HU207197B/hu not_active IP Right Cessation
-
1988
- 1988-07-15 BR BR8803563A patent/BR8803563A/pt not_active Application Discontinuation
- 1988-07-15 KR KR1019890700352A patent/KR960009483B1/ko not_active Expired - Lifetime
- 1988-07-15 CN CN88106116A patent/CN1026548C/zh not_active Expired - Fee Related
- 1988-07-15 JP JP63176859A patent/JPS6490106A/ja active Pending
- 1988-07-15 AR AR88311421A patent/AR247065A1/es active
- 1988-07-15 EP EP88306477A patent/EP0300691B1/en not_active Expired - Lifetime
- 1988-07-15 ES ES198888306477T patent/ES2037835T3/es not_active Expired - Lifetime
- 1988-07-15 DE DE8888306477T patent/DE3868751D1/de not_active Expired - Lifetime
- 1988-07-15 PL PL88273756A patent/PL161573B1/pl unknown
- 1988-07-15 US US07/220,018 patent/US4943307A/en not_active Expired - Fee Related
- 1988-07-15 AT AT88306477T patent/ATE72923T1/de not_active IP Right Cessation
- 1988-07-15 DD DD88317988A patent/DD286097A5/de not_active IP Right Cessation
- 1988-07-15 WO PCT/HU1988/000050 patent/WO1989000380A1/en not_active Ceased
- 1988-07-15 RU SU884356193A patent/RU1836011C/ru active
-
1992
- 1992-06-02 GR GR920401132T patent/GR3004781T3/el unknown
Also Published As
| Publication number | Publication date |
|---|---|
| HUT47367A (en) | 1989-03-28 |
| EP0300691B1 (en) | 1992-03-04 |
| PL273756A1 (en) | 1989-04-03 |
| WO1989000380A1 (en) | 1989-01-26 |
| CN1036124A (zh) | 1989-10-11 |
| HU207197B (en) | 1993-03-29 |
| ES2037835T3 (es) | 1993-07-01 |
| ATE72923T1 (de) | 1992-03-15 |
| JPS6490106A (en) | 1989-04-06 |
| RU1836011C (ru) | 1993-08-23 |
| DE3868751D1 (de) | 1992-04-09 |
| US4943307A (en) | 1990-07-24 |
| PL161573B1 (pl) | 1993-07-30 |
| DD286097A5 (de) | 1991-01-17 |
| EP0300691A3 (en) | 1989-02-08 |
| AR247065A1 (es) | 1994-11-30 |
| BR8803563A (pt) | 1989-02-08 |
| EP0300691A2 (en) | 1989-01-25 |
| GR3004781T3 (enExample) | 1993-04-28 |
| KR960009483B1 (ko) | 1996-07-20 |
| KR890701010A (ko) | 1989-12-19 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CN1026548C (zh) | 植物保护组合物 | |
| CN1119076C (zh) | 异噁草松的低挥发性制剂 | |
| CN1073797C (zh) | 含有二苯基醚的除草组合物及其用于除草的方法 | |
| CN1130126C (zh) | 稻田除草剂四唑啉酮类化合物 | |
| CN1034573C (zh) | 用作水稻田除莠剂的四唑啉酮 | |
| EP2770827B1 (fr) | Composition, procédé d'obtention de la composition et formulation phytosanitaire la comprenant | |
| CN1185716A (zh) | 防治哺乳动物、特别是狗和猫蚤的杀虫组合物 | |
| EP2076119B1 (fr) | Composition solvante comprenant au moins deux solvants, et formulation phytosanitaire comprenant ladite composition solvante ainsi qu' un compose actif | |
| CN1422115A (zh) | 农用制剂 | |
| CN1079637C (zh) | 植物生长调节剂组合物 | |
| CN1408221A (zh) | 基于水分散性淀粉的物理形态改进的农用试剂 | |
| CN1078043C (zh) | 杀菌剂与杀虫剂的复配物,含该复配物的组合物及其用途 | |
| JP5142608B2 (ja) | 水田用除草剤および水田の除草方法 | |
| CN1201658C (zh) | 除草制剂 | |
| CN1131509A (zh) | 磺酰氨基苯基尿嘧啶水田除草剂 | |
| CN1484491A (zh) | 基于异噁唑啉羧酸酯安全剂的除草剂－安全剂组合物 | |
| CN1252059A (zh) | 杀虫剂1－芳基－3－亚氨基吡唑 | |
| CN1250079C (zh) | 杀真菌组合物 | |
| CN1250080C (zh) | 基于霜霉威和吡啶基甲基苯甲酰胺衍生物的杀真菌组合物 | |
| CN1968604A (zh) | 除草组合物 | |
| CN1116798C (zh) | 硫线磷的微囊制剂 | |
| FR2984079A1 (fr) | Une nouvelle suspo-emulsion aqueuse | |
| CN1393134A (zh) | 含氰菌胺杀菌剂、杀虫剂组合物 | |
| CN1226135A (zh) | 用于对动物生活环境进行抗寄生虫处理的方法和组合物 | |
| CN1048850A (zh) | 新的吡唑啉及其作为解毒剂的应用 |
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 | ||
| C19 | Lapse of patent right due to non-payment of the annual fee | ||
| CF01 | Termination of patent right due to non-payment of annual fee |