SK409191A3 - Composition for plant protection based on suspoemulsion - Google Patents

Composition for plant protection based on suspoemulsion Download PDF

Info

Publication number: SK409191A3
Authority: SK; Slovakia
Prior art keywords: plant protection; organic phase; active; group; derivatives
Prior art date: 1986-09-17

Application number

SK4091-91A

Other languages

English (en)

Slovak (sk)

Inventor

Gerhard Frisch

Konrad Albrecht

Original Assignee

Hoechst Ag

Priority date (The priority date 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 date listed.)

1986-09-17

Filing date

1991-12-27

Publication date

1994-04-06

1991-12-27 Application filed by Hoechst Ag filed Critical Hoechst Ag

1994-04-06 Publication of SK409191A3 publication Critical patent/SK409191A3/sk

Links

239000000203 mixture Substances 0.000 title claims description 22
239000004548 suspo-emulsion Substances 0.000 title claims description 6
239000012074 organic phase Substances 0.000 claims abstract description 22
239000004094 surface-active agent Substances 0.000 claims abstract description 12
239000008346 aqueous phase Substances 0.000 claims abstract description 9
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims abstract description 8
229920000642 polymer Polymers 0.000 claims abstract description 8
GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 claims abstract description 6
239000003795 chemical substances by application Substances 0.000 claims abstract description 6
239000011814 protection agent Substances 0.000 claims abstract description 5
-1 β- (2-chloro-4-trifluoromethylphenoxy) -5-nitrobenzoyloxyethyl ethyl Chemical group 0.000 claims description 15
239000013543 active substance Substances 0.000 claims description 13
239000012071 phase Substances 0.000 claims description 13
150000001875 compounds Chemical class 0.000 claims description 11
239000004480 active ingredient Substances 0.000 claims description 8
150000002148 esters Chemical class 0.000 claims description 8
239000002253 acid Substances 0.000 claims description 5
MZZBPDKVEFVLFF-UHFFFAOYSA-N cyanazine Chemical compound CCNC1=NC(Cl)=NC(NC(C)(C)C#N)=N1 MZZBPDKVEFVLFF-UHFFFAOYSA-N 0.000 claims description 4
DQKWXTIYGWPGOO-UHFFFAOYSA-N (2,6-dibromo-4-cyanophenyl) octanoate Chemical compound CCCCCCCC(=O)OC1=C(Br)C=C(C#N)C=C1Br DQKWXTIYGWPGOO-UHFFFAOYSA-N 0.000 claims description 3
229910019142 PO4 Inorganic materials 0.000 claims description 3
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 3
150000007513 acids Chemical class 0.000 claims description 3
125000000217 alkyl group Chemical group 0.000 claims description 3
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 3
BACHBFVBHLGWSL-UHFFFAOYSA-N methyl 2-[4-(2,4-dichlorophenoxy)phenoxy]propanoate Chemical group C1=CC(OC(C)C(=O)OC)=CC=C1OC1=CC=C(Cl)C=C1Cl BACHBFVBHLGWSL-UHFFFAOYSA-N 0.000 claims description 3
150000002989 phenols Chemical class 0.000 claims description 3
235000021317 phosphate Nutrition 0.000 claims description 3
BACHBFVBHLGWSL-JTQLQIEISA-N rac-diclofop methyl Natural products C1=CC(O[C@@H](C)C(=O)OC)=CC=C1OC1=CC=C(Cl)C=C1Cl BACHBFVBHLGWSL-JTQLQIEISA-N 0.000 claims description 3
229910052717 sulfur Inorganic materials 0.000 claims description 3
239000011593 sulfur Substances 0.000 claims description 3
150000003918 triazines Chemical class 0.000 claims 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 claims description 3
OWZPCEFYPSAJFR-UHFFFAOYSA-N 2-(butan-2-yl)-4,6-dinitrophenol Chemical compound CCC(C)C1=CC([N+]([O-])=O)=CC([N+]([O-])=O)=C1O OWZPCEFYPSAJFR-UHFFFAOYSA-N 0.000 claims description 2
XKJMBINCVNINCA-UHFFFAOYSA-N Alfalone Chemical compound CON(C)C(=O)NC1=CC=C(Cl)C(Cl)=C1 XKJMBINCVNINCA-UHFFFAOYSA-N 0.000 claims description 2
TWFZGCMQGLPBSX-UHFFFAOYSA-N Carbendazim Natural products C1=CC=C2NC(NC(=O)OC)=NC2=C1 TWFZGCMQGLPBSX-UHFFFAOYSA-N 0.000 claims description 2
239000005892 Deltamethrin Substances 0.000 claims description 2
239000005573 Linuron Substances 0.000 claims description 2
239000005591 Pendimethalin Substances 0.000 claims description 2
239000005820 Prochloraz Substances 0.000 claims description 2
XCSGPAVHZFQHGE-UHFFFAOYSA-N alachlor Chemical compound CCC1=CC=CC(CC)=C1N(COC)C(=O)CCl XCSGPAVHZFQHGE-UHFFFAOYSA-N 0.000 claims description 2
125000002490 anilino group Chemical class [H]N(*)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 claims description 2
MXWJVTOOROXGIU-UHFFFAOYSA-N atrazine Chemical compound CCNC1=NC(Cl)=NC(NC(C)C)=N1 MXWJVTOOROXGIU-UHFFFAOYSA-N 0.000 claims description 2
JNPZQRQPIHJYNM-UHFFFAOYSA-N carbendazim Chemical compound C1=C[CH]C2=NC(NC(=O)OC)=NC2=C1 JNPZQRQPIHJYNM-UHFFFAOYSA-N 0.000 claims description 2
239000006013 carbendazim Substances 0.000 claims description 2
125000004432 carbon atom Chemical group C* 0.000 claims description 2
JXCGFZXSOMJFOA-UHFFFAOYSA-N chlorotoluron Chemical compound CN(C)C(=O)NC1=CC=C(C)C(Cl)=C1 JXCGFZXSOMJFOA-UHFFFAOYSA-N 0.000 claims description 2
229960002483 decamethrin Drugs 0.000 claims description 2
OWZREIFADZCYQD-NSHGMRRFSA-N deltamethrin Chemical compound CC1(C)[C@@H](C=C(Br)Br)[C@H]1C(=O)O[C@H](C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 OWZREIFADZCYQD-NSHGMRRFSA-N 0.000 claims description 2
230000000855 fungicidal effect Effects 0.000 claims description 2
125000005842 heteroatom Chemical group 0.000 claims description 2
CHIFOSRWCNZCFN-UHFFFAOYSA-N pendimethalin Chemical compound CCC(CC)NC1=C([N+]([O-])=O)C=C(C)C(C)=C1[N+]([O-])=O CHIFOSRWCNZCFN-UHFFFAOYSA-N 0.000 claims description 2
150000003013 phosphoric acid derivatives Chemical class 0.000 claims description 2
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 2
ODCWYMIRDDJXKW-UHFFFAOYSA-N simazine Chemical compound CCNC1=NC(Cl)=NC(NCC)=N1 ODCWYMIRDDJXKW-UHFFFAOYSA-N 0.000 claims description 2
150000003852 triazoles Chemical class 0.000 claims description 2
239000004476 plant protection product Substances 0.000 claims 4
241000196324 Embryophyta Species 0.000 claims 3
LUBJCRLGQSPQNN-UHFFFAOYSA-N 1-Phenylurea Chemical class NC(=O)NC1=CC=CC=C1 LUBJCRLGQSPQNN-UHFFFAOYSA-N 0.000 claims 2
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Natural products CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 claims 2
AAILEWXSEQLMNI-UHFFFAOYSA-N 1h-pyridazin-6-one Chemical class OC1=CC=CN=N1 AAILEWXSEQLMNI-UHFFFAOYSA-N 0.000 claims 1
TVFWYUWNQVRQRG-UHFFFAOYSA-N 2,3,4-tris(2-phenylethenyl)phenol Chemical class C=1C=CC=CC=1C=CC1=C(C=CC=2C=CC=CC=2)C(O)=CC=C1C=CC1=CC=CC=C1 TVFWYUWNQVRQRG-UHFFFAOYSA-N 0.000 claims 1
ZGYDSBDLZFDVSG-UHFFFAOYSA-N 2,4-dioxoimidazolidine-1-carboxamide Chemical class NC(=O)N1CC(=O)NC1=O ZGYDSBDLZFDVSG-UHFFFAOYSA-N 0.000 claims 1
UBRAQXSCQXIDLI-UHFFFAOYSA-N 2-(4-amino-3,5-dichloro-6-fluoropyridin-2-yl)acetic acid Chemical compound NC1=C(Cl)C(F)=NC(CC(O)=O)=C1Cl UBRAQXSCQXIDLI-UHFFFAOYSA-N 0.000 claims 1
WVQBLGZPHOPPFO-UHFFFAOYSA-N 2-chloro-N-(2-ethyl-6-methylphenyl)-N-(1-methoxypropan-2-yl)acetamide Chemical compound CCC1=CC=CC(C)=C1N(C(C)COC)C(=O)CCl WVQBLGZPHOPPFO-UHFFFAOYSA-N 0.000 claims 1
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 1
240000005979 Hordeum vulgare Species 0.000 claims 1
235000007340 Hordeum vulgare Nutrition 0.000 claims 1
QBEXFUOWUYCXNI-UHFFFAOYSA-N Ioxynil octanoate Chemical compound CCCCCCCC(=O)OC1=C(I)C=C(C#N)C=C1I QBEXFUOWUYCXNI-UHFFFAOYSA-N 0.000 claims 1
239000005867 Iprodione Substances 0.000 claims 1
239000005822 Propiconazole Substances 0.000 claims 1
RDYMFSUJUZBWLH-SVWSLYAFSA-N endosulfan Chemical compound C([C@@H]12)OS(=O)OC[C@@H]1[C@]1(Cl)C(Cl)=C(Cl)[C@@]2(Cl)C1(Cl)Cl RDYMFSUJUZBWLH-SVWSLYAFSA-N 0.000 claims 1
BFWMWWXRWVJXSE-UHFFFAOYSA-M fentin hydroxide Chemical compound C=1C=CC=CC=1[Sn](C=1C=CC=CC=1)(O)C1=CC=CC=C1 BFWMWWXRWVJXSE-UHFFFAOYSA-M 0.000 claims 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 claims 1
PUIYMUZLKQOUOZ-UHFFFAOYSA-N isoproturon Chemical compound CC(C)C1=CC=C(NC(=O)N(C)C)C=C1 PUIYMUZLKQOUOZ-UHFFFAOYSA-N 0.000 claims 1
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 1
230000001755 vocal effect Effects 0.000 claims 1
239000002904 solvent Substances 0.000 description 5
239000000654 additive Substances 0.000 description 4
229910052783 alkali metal Inorganic materials 0.000 description 4
WSFSSNUMVMOOMR-UHFFFAOYSA-N formaldehyde Substances O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 4
238000009472 formulation Methods 0.000 description 4
239000000725 suspension Substances 0.000 description 4
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
239000003153 chemical reaction reagent Substances 0.000 description 3
RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 3
229920001296 polysiloxane Polymers 0.000 description 3
239000000047 product Substances 0.000 description 3
150000003839 salts Chemical class 0.000 description 3
IYIRBMFFGGJLPK-UHFFFAOYSA-N C(CC)(=O)O.O(C1=CC=CC=C1)CC(=O)O Chemical class C(CC)(=O)O.O(C1=CC=CC=C1)CC(=O)O IYIRBMFFGGJLPK-UHFFFAOYSA-N 0.000 description 2
229910052782 aluminium Inorganic materials 0.000 description 2
230000015572 biosynthetic process Effects 0.000 description 2
239000013078 crystal Substances 0.000 description 2
239000006185 dispersion Substances 0.000 description 2
238000004090 dissolution Methods 0.000 description 2
238000000034 method Methods 0.000 description 2
239000003960 organic solvent Substances 0.000 description 2
239000007790 solid phase Substances 0.000 description 2
239000000126 substance Substances 0.000 description 2
XFRVVPUIAFSTFO-UHFFFAOYSA-N 1-Tridecanol Chemical compound CCCCCCCCCCCCCO XFRVVPUIAFSTFO-UHFFFAOYSA-N 0.000 description 1
NMIZONYLXCOHEF-UHFFFAOYSA-N 1h-imidazole-2-carboxamide Chemical class NC(=O)C1=NC=CN1 NMIZONYLXCOHEF-UHFFFAOYSA-N 0.000 description 1
WNTGYJSOUMFZEP-UHFFFAOYSA-N 2-(4-chloro-2-methylphenoxy)propanoic acid Chemical compound OC(=O)C(C)OC1=CC=C(Cl)C=C1C WNTGYJSOUMFZEP-UHFFFAOYSA-N 0.000 description 1
YUVKUEAFAVKILW-UHFFFAOYSA-N 2-(4-{[5-(trifluoromethyl)pyridin-2-yl]oxy}phenoxy)propanoic acid Chemical compound C1=CC(OC(C)C(O)=O)=CC=C1OC1=CC=C(C(F)(F)F)C=N1 YUVKUEAFAVKILW-UHFFFAOYSA-N 0.000 description 1
CSIJFRLUCALOQZ-UHFFFAOYSA-N 2-acetyloxyethyl 5-[2-chloro-4-(trifluoromethyl)phenoxy]-2-nitrobenzoate Chemical compound C1=C([N+]([O-])=O)C(C(=O)OCCOC(=O)C)=CC(OC=2C(=CC(=CC=2)C(F)(F)F)Cl)=C1 CSIJFRLUCALOQZ-UHFFFAOYSA-N 0.000 description 1
CVNOWLNNPYYEOH-UHFFFAOYSA-N 4-cyanophenol Chemical compound OC1=CC=C(C#N)C=C1 CVNOWLNNPYYEOH-UHFFFAOYSA-N 0.000 description 1
ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
MQIUGAXCHLFZKX-UHFFFAOYSA-N Di-n-octyl phthalate Natural products CCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC MQIUGAXCHLFZKX-UHFFFAOYSA-N 0.000 description 1
PQKBPHSEKWERTG-UHFFFAOYSA-N Fenoxaprop ethyl Chemical group C1=CC(OC(C)C(=O)OCC)=CC=C1OC1=NC2=CC=C(Cl)C=C2O1 PQKBPHSEKWERTG-UHFFFAOYSA-N 0.000 description 1
206010026749 Mania Diseases 0.000 description 1
LKJPSUCKSLORMF-UHFFFAOYSA-N Monolinuron Chemical compound CON(C)C(=O)NC1=CC=C(Cl)C=C1 LKJPSUCKSLORMF-UHFFFAOYSA-N 0.000 description 1
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
HDVZSCYWPDXPLN-UHFFFAOYSA-N O1N=C(C=C1)C=1C(=C(C(=O)N)C(=CC1)OC)OC Chemical compound O1N=C(C=C1)C=1C(=C(C(=O)N)C(=CC1)OC)OC HDVZSCYWPDXPLN-UHFFFAOYSA-N 0.000 description 1
ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
229910052910 alkali metal silicate Inorganic materials 0.000 description 1
150000001340 alkali metals Chemical class 0.000 description 1
XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
229910000323 aluminium silicate Inorganic materials 0.000 description 1
150000003863 ammonium salts Chemical class 0.000 description 1
239000007798 antifreeze agent Substances 0.000 description 1
150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
125000003118 aryl group Chemical group 0.000 description 1
WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 1
VEMKTZHHVJILDY-UXHICEINSA-N bioresmethrin Chemical compound CC1(C)[C@H](C=C(C)C)[C@H]1C(=O)OCC1=COC(CC=2C=CC=CC=2)=C1 VEMKTZHHVJILDY-UXHICEINSA-N 0.000 description 1
BJQHLKABXJIVAM-UHFFFAOYSA-N bis(2-ethylhexyl) phthalate Chemical compound CCCCC(CC)COC(=O)C1=CC=CC=C1C(=O)OCC(CC)CCCC BJQHLKABXJIVAM-UHFFFAOYSA-N 0.000 description 1
239000004202 carbamide Substances 0.000 description 1
229910052799 carbon Inorganic materials 0.000 description 1
239000000084 colloidal system Substances 0.000 description 1
230000000052 comparative effect Effects 0.000 description 1
239000012141 concentrate Substances 0.000 description 1
238000009833 condensation Methods 0.000 description 1
230000005494 condensation Effects 0.000 description 1
239000007859 condensation product Substances 0.000 description 1
229910052593 corundum Inorganic materials 0.000 description 1
239000010431 corundum Substances 0.000 description 1
QNLZIZAQLLYXTC-UHFFFAOYSA-N dimethylnaphthalene Natural products C1=CC=CC2=C(C)C(C)=CC=C21 QNLZIZAQLLYXTC-UHFFFAOYSA-N 0.000 description 1
239000002270 dispersing agent Substances 0.000 description 1
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 description 1
108010074629 endosulfine Proteins 0.000 description 1
102000008110 endosulfine Human genes 0.000 description 1
239000012530 fluid Substances 0.000 description 1
230000008014 freezing Effects 0.000 description 1
238000007710 freezing Methods 0.000 description 1
239000012535 impurity Substances 0.000 description 1
229910052740 iodine Inorganic materials 0.000 description 1
239000011630 iodine Substances 0.000 description 1
150000002576 ketones Chemical class 0.000 description 1
FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
229920000847 nonoxynol Polymers 0.000 description 1
229920003986 novolac Polymers 0.000 description 1
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
150000003021 phthalic acid derivatives Chemical class 0.000 description 1
229920000151 polyglycol Polymers 0.000 description 1
239000010695 polyglycol Substances 0.000 description 1
239000003755 preservative agent Substances 0.000 description 1
108090000623 proteins and genes Proteins 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
150000004760 silicates Chemical class 0.000 description 1
159000000000 sodium salts Chemical class 0.000 description 1
239000007787 solid Substances 0.000 description 1
230000000087 stabilizing effect Effects 0.000 description 1
238000003756 stirring Methods 0.000 description 1
239000001384 succinic acid Substances 0.000 description 1
229910021653 sulphate ion Inorganic materials 0.000 description 1
VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical class ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 1
STCOOQWBFONSKY-UHFFFAOYSA-N tributyl phosphate Chemical compound CCCCOP(=O)(OCCCC)OCCCC STCOOQWBFONSKY-UHFFFAOYSA-N 0.000 description 1
229940087291 tridecyl alcohol Drugs 0.000 description 1
NFHRNKANAAGQOH-UHFFFAOYSA-N triphenylstannane Chemical compound C1=CC=CC=C1[SnH](C=1C=CC=CC=1)C1=CC=CC=C1 NFHRNKANAAGQOH-UHFFFAOYSA-N 0.000 description 1
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
238000001238 wet grinding Methods 0.000 description 1
239000000080 wetting agent Substances 0.000 description 1
239000008096 xylene Substances 0.000 description 1

Classifications

- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- 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)
Dentistry (AREA)
Dispersion Chemistry (AREA)
Pest Control & Pesticides (AREA)
Plant Pathology (AREA)
Chemical & Material Sciences (AREA)
Engineering & Computer Science (AREA)
Agronomy & Crop Science (AREA)
Wood Science & Technology (AREA)
Zoology (AREA)
Environmental Sciences (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Compositions Of Macromolecular Compounds (AREA)
Paints Or Removers (AREA)
Breeding Of Plants And Reproduction By Means Of Culturing (AREA)

SK4091-91A 1986-09-17 1991-12-27 Composition for plant protection based on suspoemulsion SK409191A3 (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE19863631558 DE3631558A1 (de)	1986-09-17	1986-09-17	Neue suspoemulsionen von pflanzenschutz-wirkstoffen

Publications (1)

Publication Number	Publication Date
SK409191A3 true SK409191A3 (en)	1994-04-06

Family

ID=6309733

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
SK4091-91A SK409191A3 (en)	1986-09-17	1991-12-27	Composition for plant protection based on suspoemulsion

Country Status (14)

Country	Link
US (1)	US5074905A (fr)
EP (1)	EP0261492B1 (fr)
JP (1)	JP2593886B2 (fr)
AT (1)	ATE131002T1 (fr)
AU (1)	AU599701B2 (fr)
CA (1)	CA1302106C (fr)
CZ (1)	CZ409191A3 (fr)
DE (2)	DE3631558A1 (fr)
DK (1)	DK174857B1 (fr)
ES (1)	ES2082741T3 (fr)
HU (1)	HU204392B (fr)
IL (1)	IL83914A (fr)
SK (1)	SK409191A3 (fr)
ZA (1)	ZA876954B (fr)

Families Citing this family (31)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US5461027A (en) *	1989-01-24	1995-10-24	Griffin Corporation	Microencapsulated pendimethalin and method of making and using same
US5599768A (en) *	1989-09-21	1997-02-04	E. I. Du Pont De Nemours And Company	Stabilization of non-aqueous suspensions
FR2670086A1 (fr) *	1990-12-10	1992-06-12	Rhone Poulenc Chimie	Suspo-emulsions phytosanitaires.
FR2673508B1 (fr) *	1991-03-06	1993-06-25	Rhone Poulenc Chimie	Suspo-emulsions phytosanitaires.
DK0514769T3 (fr) *	1991-05-18	1997-02-10	Hoechst Schering Agrevo Gmbh
ATE161389T1 (de) *	1991-09-14	1998-01-15	Hoechst Schering Agrevo Gmbh	Selektive herbizide mittel in form konzentrierter mikroemulsionen
EP0541056B1 (fr) *	1991-11-08	1996-06-12	Hoechst Schering AgrEvo GmbH	Granulés dispersibles dans l'eau de suspoémulsions
GB9203429D0 (en) *	1992-02-18	1992-04-01	Schering Agrochemicals Ltd	Pesticidal compositions
DE4322211A1 (de) *	1993-07-03	1995-01-12	Basf Ag	Wäßrige, mehrphasige, stabile Fertigformulierung für Pflanzenschutz-Wirkstoffe und Verfahren zu ihrer Herstellung
FR2707181B1 (fr) *	1993-07-07	1995-08-18	Rhone Poulenc Geronazzo Spa	Formulations concentrées fluide de dérivés de tristyrylphénol polyalkoxylé phosphatés utilisables notamment en agrochimie.
ES2117748T3 (es) *	1993-11-16	1998-08-16	Bayer Ag	Empleo de esteres del acido fosforico como inhibidores de cristalizacion.
GB9413980D0 (en) *	1994-07-12	1994-08-31	Rohm & Haas France	Novel agrochemical formulation
US6358909B1 (en)	1996-10-17	2002-03-19	The Clorox Company	Suspoemulsion system for delivery of actives
EP0882498B1 (fr) *	1997-06-02	2004-02-11	Hodogaya Chemical Co Ltd	Procédé de préparation d'émulsions d'huile dans l'eau sans solvent
MY118564A (en)	1998-02-10	2004-12-31	Syngenta Participations Ag	Pesticidal compositions
BR9908696B1 (pt) *	1998-03-09	2011-05-31		composição herbicida e método de controle de ervas daninhas em um campo.
DE19834028A1 (de) *	1998-07-28	2000-02-03	Wolman Gmbh Dr	Verfahren zur Behandlung von Holz gegen den Befall durch holzschädigende Pilze
GB9816697D0 (en) *	1998-07-31	1998-09-30	Agrevo Uk Ltd	Liquid formulations
WO2000035284A1 (fr) *	1998-12-17	2000-06-22	Syngenta Participations Ag .	Concentres pesticides sous forme de suspensions aqueuses
WO2000060941A1 (fr) *	1999-04-09	2000-10-19	Sankyo Company, Limited	Preparations de pesticide solide flottant
DE19963381A1 (de) *	1999-12-28	2001-07-12	Aventis Cropscience Gmbh	Tensid/Lösungsmittel-Systeme
DE10028411A1 (de) *	2000-06-08	2002-02-21	Bayer Ag	Feststoffpräparationen
DE10063960A1 (de) *	2000-12-20	2002-06-27	Aventis Cropscience Gmbh	Herbizide Mittel
DE10258867A1 (de) *	2002-12-17	2004-07-08	Bayer Cropscience Gmbh	Mikroemulsionskonzentrate
GB0405760D0 (en) *	2004-03-15	2004-04-21	Syngenta Participations Ag	Agrochemical formulation
NZ564019A (en) *	2005-06-10	2010-01-29	Bayer Cropscience Ag	Oil-in-water suspoemulsions containing phytoactive hydroxybenzonitriles
ES2692427T3 (es)	2006-09-22	2018-12-03	Huntsman Petrochemical Llc	Inhibición de la maduración de ostwald en formulaciones químicas
BRPI0810022B1 (pt) *	2007-04-25	2018-08-28	Basf Se	composição
CN101848639A (zh) *	2007-07-20	2010-09-29	巴斯夫欧洲公司	含有醇烷氧基化物的组合物以及醇烷氧基化物在农业化学领域作为辅助剂的用途
JP2011518909A (ja) *	2008-04-24	2011-06-30	ビーエーエスエフソシエタス・ヨーロピア	アルコールアルコキシレート、それを含む作用剤、および農薬分野におけるアジュバントとしてのアルコールアルコキシレートの使用
CN102067860B (zh) *	2011-01-13	2013-06-05	四川农业大学	一种多菌灵微乳剂及其制备方法

Family Cites Families (16)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US3373010A (en) *	1964-10-08	1968-03-12	Du Pont	Herbicidal composition and method
NL6816772A (fr) *	1967-11-28	1969-05-30
US4295877A (en) *	1977-06-24	1981-10-20	Philagro	Selective herbicidal method in cotton and soybeans
DE2909158A1 (de) *	1979-03-08	1980-09-11	Basf Ag	Herbizide mischungen
DE2924403A1 (de) *	1979-06-16	1980-12-18	Hoechst Ag	Herbizide mittel
IT1131750B (it) *	1980-06-06	1986-06-25	Montedison Spa	Formulazioni stabili di n-(3,4-diclorofenil)-n'metossi-n'-metilurea (linorun) e 2,6-dinitor-n,n-dipropil-4-trifluoro metilanilina (trifluralin) in emulsione
DE3033335A1 (de) *	1980-09-04	1982-04-22	Lentia GmbH Chem. u. pharm. Erzeugnisse - Industriebedarf, 8000 München	Verfahren zur herstellung einer lagerstabilen, konzentrierten emulsion von herbizid wirkenden phenoxyalkancarbonsaeureestern
US4461641A (en) *	1982-02-25	1984-07-24	Ciba-Geigy Corporation	Herbicidal mixtures
EP0089268B1 (fr) *	1982-03-05	1986-07-02	Stauffer Chemical Company	Composition herbicide liquide à base de thiolcarbamate-triazine
DE3240862A1 (de) *	1982-11-05	1984-05-10	Hoechst Ag, 6230 Frankfurt	Fluessige pestizide mittel in form von suspensionskonzentraten
DE3302648A1 (de) *	1983-01-27	1984-08-02	Hoechst Ag, 6230 Frankfurt	Pflanzenschutzmittel in form von mischdispersionen
EP0142485B1 (fr) *	1983-09-19	1989-03-01	Monsanto Company	Formulation, pouvant s'écouler, sous forme d'émulsion contenant un mélange alachlor/atrazine comme agent actif
EP0143099B1 (fr) *	1983-09-19	1989-02-01	Monsanto Company	Formulation pouvant s'écouler, stable à l'entreposage, sous forme d'émulsion, contenant un mélange alachlor/atrazine comme agent actif
DE3571117D1 (en) *	1984-07-16	1989-07-27	Ciba Geigy Ag	Biocidal composition
DE3508642A1 (de) *	1985-03-12	1986-09-18	Bayer Ag, 5090 Leverkusen	Makroemulsionen
DE3542440A1 (de) *	1985-11-30	1987-06-04	Hoechst Ag	Neue wasserdispergierbare granulate

1986
- 1986-09-17 DE DE19863631558 patent/DE3631558A1/de not_active Withdrawn
1987
- 1987-09-08 ES ES87113082T patent/ES2082741T3/es not_active Expired - Lifetime
- 1987-09-08 DE DE3751627T patent/DE3751627D1/de not_active Expired - Lifetime
- 1987-09-08 AT AT87113082T patent/ATE131002T1/de not_active IP Right Cessation
- 1987-09-08 EP EP87113082A patent/EP0261492B1/fr not_active Expired - Lifetime
- 1987-09-16 IL IL83914A patent/IL83914A/xx not_active IP Right Cessation
- 1987-09-16 AU AU78476/87A patent/AU599701B2/en not_active Expired
- 1987-09-16 ZA ZA876954A patent/ZA876954B/xx unknown
- 1987-09-16 CA CA000546974A patent/CA1302106C/fr not_active Expired - Lifetime
- 1987-09-16 JP JP62229956A patent/JP2593886B2/ja not_active Expired - Lifetime
- 1987-09-16 HU HU874114A patent/HU204392B/hu not_active IP Right Cessation
- 1987-09-16 DK DK198704857A patent/DK174857B1/da not_active IP Right Cessation
1989
- 1989-11-20 US US07/438,978 patent/US5074905A/en not_active Expired - Lifetime
1991
- 1991-12-27 CZ CS914091A patent/CZ409191A3/cs unknown
- 1991-12-27 SK SK4091-91A patent/SK409191A3/sk unknown

Also Published As

Publication number	Publication date
DK485787A (da)	1988-03-18
HUT44894A (en)	1988-05-30
DK174857B1 (da)	2003-12-29
AU7847687A (en)	1988-03-24
DK485787D0 (da)	1987-09-16
US5074905A (en)	1991-12-24
IL83914A0 (en)	1988-02-29
DE3751627D1 (de)	1996-01-18
ATE131002T1 (de)	1995-12-15
EP0261492A3 (en)	1990-12-05
ES2082741T3 (es)	1996-04-01
ZA876954B (en)	1988-03-21
DE3631558A1 (de)	1988-03-31
CZ409191A3 (en)	1993-07-14
HU204392B (en)	1992-01-28
IL83914A (en)	1991-05-12
JPS6383001A (ja)	1988-04-13
EP0261492B1 (fr)	1995-12-06
JP2593886B2 (ja)	1997-03-26
AU599701B2 (en)	1990-07-26
CA1302106C (fr)	1992-06-02
EP0261492A2 (fr)	1988-03-30

Publication	Publication Date	Title
SK409191A3 (en)	1994-04-06	Composition for plant protection based on suspoemulsion
JP3152991B2 (ja)	2001-04-03	液状除草剤組成物
CZ302078B6 (cs)	2010-09-29	Kapalný prípravek úcinných látek
DK175268B1 (da)	2004-08-02	Pesticidpræparat og fremgangsmåde til fremstilling heraf
US4594096A (en)	1986-06-10	Plant protection agents in the form of mixed dispersions
FI90187B (fi)	1993-09-30	Pendimetaliinin väkevöityjä vesisuspensiokoostumuksia
JPS63236532A (ja)	1988-10-03	水中油型エマルシヨン、その製造方法および使用方法
JPS5998002A (ja)	1984-06-06	懸濁液濃縮物の形態の液状農薬組成物
CN103501596B (zh)	2016-10-05	用于提高农业油基悬浮制剂的物理稳定性的组合物和方法
JPS63310801A (ja)	1988-12-19	液体農薬組成物
JP2011505459A (ja)	2011-02-24	ラテックス塗料用の殺生物剤、グラインドおよび分散相を含有するラテックス塗料の製造方法
CN106028812B (zh)	2020-06-12	制备甲霜灵的含水共配制剂的方法
JPS6333303A (ja)	1988-02-13	水性懸濁濃厚組成物
JP2003506464A (ja)	2003-02-18	外部寄生虫殺虫性の水性懸濁製剤
JP3293867B2 (ja)	2002-06-17	グルフオシネートを基礎とした除草剤混合物の液体調合物
JPH0696481B2 (ja)	1994-11-30	微細に分散された液体の植物保護剤およびその製造方法
JPH06505971A (ja)	1994-07-07	殺かび性組成物
JPS62132801A (ja)	1987-06-16	水性乳濁液を基礎とした植物保護剤
CS266343B2 (en)	1989-12-13	Emulsion of /e/-0-2-isopropoxycarbonyl-1-methylvinyl-0-methylethylphosphoramidothionate
JP5232025B2 (ja)	2013-07-10	安定化された水性懸濁製剤
US6143830A (en)	2000-11-07	Emulsifier composition comprising ethylene oxide/propylene oxide block copolymers and amine-containing ethylene oxide/propylene oxide block copolymers
HU204653B (en)	1992-02-28	Method for making combined liquid plant protecting preparative
CA1298546C (fr)	1992-04-07	Compositions aqueuses pesticides, s'ecoulant librement
US20070292465A1 (en)	2007-12-20	Eutectic biocide compositions and formulations
JP2000302601A (ja)	2000-10-31	工業用殺菌剤