IL97498A - Pesticidal compositions comprising water-soluble heat-activated binder - Google Patents

Pesticidal compositions comprising water-soluble heat-activated binder

Info

Publication number: IL97498A
Authority: IL; Israel
Prior art keywords: water; composition; granules; binder; soluble
Prior art date: 1990-03-12

Application number

IL9749891A

Other languages

English (en)

Other versions

IL97498A0 (en

Original Assignee

Du Pont

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.)

1990-03-12

Filing date

1991-03-11

Publication date

1995-07-31

1991-03-11 Application filed by Du Pont filed Critical Du Pont

1992-06-21 Publication of IL97498A0 publication Critical patent/IL97498A0/xx

1995-07-31 Publication of IL97498A publication Critical patent/IL97498A/en

Links

239000000203 mixture Substances 0.000 title claims abstract description 50
239000011230 binding agent Substances 0.000 title claims abstract description 29
230000000361 pesticidal effect Effects 0.000 title claims abstract description 21
239000002245 particle Substances 0.000 claims abstract description 22
239000007787 solid Substances 0.000 claims abstract description 8
239000008187 granular material Substances 0.000 claims description 71
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 33
238000002844 melting Methods 0.000 claims description 20
230000008018 melting Effects 0.000 claims description 20
239000000575 pesticide Substances 0.000 claims description 16
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims description 12
238000004090 dissolution Methods 0.000 claims description 10
JKTAIYGNOFSMCE-UHFFFAOYSA-N 2,3-di(nonyl)phenol Polymers CCCCCCCCCC1=CC=CC(O)=C1CCCCCCCCC JKTAIYGNOFSMCE-UHFFFAOYSA-N 0.000 claims description 9
238000007711 solidification Methods 0.000 claims description 9
230000008023 solidification Effects 0.000 claims description 9
239000000654 additive Substances 0.000 claims description 8
229920001577 copolymer Polymers 0.000 claims description 8
239000000155 melt Substances 0.000 claims description 7
HQQADJVZYDDRJT-UHFFFAOYSA-N ethene;prop-1-ene Chemical group C=C.CC=C HQQADJVZYDDRJT-UHFFFAOYSA-N 0.000 claims 4
230000000996 additive effect Effects 0.000 claims 1
150000001768 cations Chemical class 0.000 claims 1
239000000126 substance Substances 0.000 description 26
238000000034 method Methods 0.000 description 20
238000004062 sedimentation Methods 0.000 description 15
238000005469 granulation Methods 0.000 description 14
230000003179 granulation Effects 0.000 description 14
125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 14
230000008569 process Effects 0.000 description 13
125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 12
229910052708 sodium Inorganic materials 0.000 description 12
DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 11
239000011734 sodium Substances 0.000 description 11
XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 10
QPJVMBTYPHYUOC-UHFFFAOYSA-N methyl benzoate Chemical compound COC(=O)C1=CC=CC=C1 QPJVMBTYPHYUOC-UHFFFAOYSA-N 0.000 description 9
-1 polyoxyethylene Polymers 0.000 description 9
239000005496 Chlorsulfuron Substances 0.000 description 8
VJYIFXVZLXQVHO-UHFFFAOYSA-N chlorsulfuron Chemical compound COC1=NC(C)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2)Cl)=N1 VJYIFXVZLXQVHO-UHFFFAOYSA-N 0.000 description 8
239000000463 material Substances 0.000 description 8
125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 description 8
238000003556 assay Methods 0.000 description 7
239000006185 dispersion Substances 0.000 description 7
238000012360 testing method Methods 0.000 description 7
239000004202 carbamide Substances 0.000 description 6
RPACBEVZENYWOL-XFULWGLBSA-M sodium;(2r)-2-[6-(4-chlorophenoxy)hexyl]oxirane-2-carboxylate Chemical compound [Na+].C=1C=C(Cl)C=CC=1OCCCCCC[C@]1(C(=O)[O-])CO1 RPACBEVZENYWOL-XFULWGLBSA-M 0.000 description 6
238000005507 spraying Methods 0.000 description 6
239000005631 2,4-Dichlorophenoxyacetic acid Substances 0.000 description 5
239000002253 acid Substances 0.000 description 5
230000032683 aging Effects 0.000 description 5
WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 5
238000009472 formulation Methods 0.000 description 5
238000002156 mixing Methods 0.000 description 5
239000002904 solvent Substances 0.000 description 5
KXDAEFPNCMNJSK-UHFFFAOYSA-N Benzamide Chemical compound NC(=O)C1=CC=CC=C1 KXDAEFPNCMNJSK-UHFFFAOYSA-N 0.000 description 4
CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 4
150000003863 ammonium salts Chemical class 0.000 description 4
238000001816 cooling Methods 0.000 description 4
238000000354 decomposition reaction Methods 0.000 description 4
238000000113 differential scanning calorimetry Methods 0.000 description 4
238000010790 dilution Methods 0.000 description 4
239000012895 dilution Substances 0.000 description 4
WSFSSNUMVMOOMR-UHFFFAOYSA-N formaldehyde Substances O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 4
238000010438 heat treatment Methods 0.000 description 4
239000004615 ingredient Substances 0.000 description 4
230000000704 physical effect Effects 0.000 description 4
239000000243 solution Substances 0.000 description 4
239000001692 EU approved anti-caking agent Substances 0.000 description 3
102000004190 Enzymes Human genes 0.000 description 3
108090000790 Enzymes Proteins 0.000 description 3
241001024304 Mino Species 0.000 description 3
UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 3
IGFHQQFPSIBGKE-UHFFFAOYSA-N Nonylphenol Natural products CCCCCCCCCC1=CC=C(O)C=C1 IGFHQQFPSIBGKE-UHFFFAOYSA-N 0.000 description 3
GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 3
TWFZGCMQGLPBSX-UHFFFAOYSA-N carbendazim Chemical compound C1=CC=C2NC(NC(=O)OC)=NC2=C1 TWFZGCMQGLPBSX-UHFFFAOYSA-N 0.000 description 3
238000005056 compaction Methods 0.000 description 3
239000004148 curcumin Substances 0.000 description 3
239000007884 disintegrant Substances 0.000 description 3
239000002270 dispersing agent Substances 0.000 description 3
238000001035 drying Methods 0.000 description 3
239000004009 herbicide Substances 0.000 description 3
239000002917 insecticide Substances 0.000 description 3
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 3
239000007788 liquid Substances 0.000 description 3
238000005259 measurement Methods 0.000 description 3
150000004702 methyl esters Chemical class 0.000 description 3
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 3
SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical compound CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 3
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 3
229920001983 poloxamer Polymers 0.000 description 3
235000017281 sodium acetate Nutrition 0.000 description 3
239000003381 stabilizer Substances 0.000 description 3
229910001220 stainless steel Inorganic materials 0.000 description 3
239000010935 stainless steel Substances 0.000 description 3
238000009736 wetting Methods 0.000 description 3
YIKWKLYQRFRGPM-UHFFFAOYSA-N 1-dodecylguanidine acetate Chemical compound CC(O)=O.CCCCCCCCCCCCN=C(N)N YIKWKLYQRFRGPM-UHFFFAOYSA-N 0.000 description 2
QPUYECUOLPXSFR-UHFFFAOYSA-N 1-methylnaphthalene Chemical compound C1=CC=C2C(C)=CC=CC2=C1 QPUYECUOLPXSFR-UHFFFAOYSA-N 0.000 description 2
YIVXMZJTEQBPQO-UHFFFAOYSA-N 2,4-DB Chemical compound OC(=O)CCCOC1=CC=C(Cl)C=C1Cl YIVXMZJTEQBPQO-UHFFFAOYSA-N 0.000 description 2
YOYAIZYFCNQIRF-UHFFFAOYSA-N 2,6-dichlorobenzonitrile Chemical compound ClC1=CC=CC(Cl)=C1C#N YOYAIZYFCNQIRF-UHFFFAOYSA-N 0.000 description 2
MZHCENGPTKEIGP-UHFFFAOYSA-N 2-(2,4-dichlorophenoxy)propanoic acid Chemical compound OC(=O)C(C)OC1=CC=C(Cl)C=C1Cl MZHCENGPTKEIGP-UHFFFAOYSA-N 0.000 description 2
BDKLKNJTMLIAFE-UHFFFAOYSA-N 2-(3-fluorophenyl)-1,3-oxazole-4-carbaldehyde Chemical compound FC1=CC=CC(C=2OC=C(C=O)N=2)=C1 BDKLKNJTMLIAFE-UHFFFAOYSA-N 0.000 description 2
LLWADFLAOKUBDR-UHFFFAOYSA-N 2-methyl-4-chlorophenoxybutyric acid Chemical compound CC1=CC(Cl)=CC=C1OCCCC(O)=O LLWADFLAOKUBDR-UHFFFAOYSA-N 0.000 description 2
UBPQITZLYDWRFS-UHFFFAOYSA-N 3,4-dihydro-1H-triazine-2,4-diamine Chemical compound NC1NN(N)NC=C1 UBPQITZLYDWRFS-UHFFFAOYSA-N 0.000 description 2
UPMXNNIRAGDFEH-UHFFFAOYSA-N 3,5-dibromo-4-hydroxybenzonitrile Chemical compound OC1=C(Br)C=C(C#N)C=C1Br UPMXNNIRAGDFEH-UHFFFAOYSA-N 0.000 description 2
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 description 2
239000005711 Benzoic acid Substances 0.000 description 2
HSSBORCLYSCBJR-UHFFFAOYSA-N Chloramben Chemical compound NC1=CC(Cl)=CC(C(O)=O)=C1Cl HSSBORCLYSCBJR-UHFFFAOYSA-N 0.000 description 2
VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 2
XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
239000005575 MCPB Substances 0.000 description 2
FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 2
OKIBNKKYNPBDRS-UHFFFAOYSA-N Mefluidide Chemical compound CC(=O)NC1=CC(NS(=O)(=O)C(F)(F)F)=C(C)C=C1C OKIBNKKYNPBDRS-UHFFFAOYSA-N 0.000 description 2
RRVIAQKBTUQODI-UHFFFAOYSA-N Methabenzthiazuron Chemical compound C1=CC=C2SC(N(C)C(=O)NC)=NC2=C1 RRVIAQKBTUQODI-UHFFFAOYSA-N 0.000 description 2
229920000168 Microcrystalline cellulose Polymers 0.000 description 2
229920003171 Poly (ethylene oxide) Polymers 0.000 description 2
JXVIIQLNUPXOII-UHFFFAOYSA-N Siduron Chemical compound CC1CCCCC1NC(=O)NC1=CC=CC=C1 JXVIIQLNUPXOII-UHFFFAOYSA-N 0.000 description 2
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
239000004115 Sodium Silicate Substances 0.000 description 2
229940100389 Sulfonylurea Drugs 0.000 description 2
HBPDKDSFLXWOAE-UHFFFAOYSA-N Tebuthiuron Chemical compound CNC(=O)N(C)C1=NN=C(C(C)(C)C)S1 HBPDKDSFLXWOAE-UHFFFAOYSA-N 0.000 description 2
WHKUVVPPKQRRBV-UHFFFAOYSA-N Trasan Chemical compound CC1=CC(Cl)=CC=C1OCC(O)=O WHKUVVPPKQRRBV-UHFFFAOYSA-N 0.000 description 2
239000000642 acaricide Substances 0.000 description 2
239000011149 active material Substances 0.000 description 2
229910052782 aluminium Inorganic materials 0.000 description 2
XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
239000003899 bactericide agent Substances 0.000 description 2
235000010233 benzoic acid Nutrition 0.000 description 2
229920001400 block copolymer Polymers 0.000 description 2
WYKYKTKDBLFHCY-UHFFFAOYSA-N chloridazon Chemical compound O=C1C(Cl)=C(N)C=NN1C1=CC=CC=C1 WYKYKTKDBLFHCY-UHFFFAOYSA-N 0.000 description 2
CRQQGFGUEAVUIL-UHFFFAOYSA-N chlorothalonil Chemical compound ClC1=C(Cl)C(C#N)=C(Cl)C(C#N)=C1Cl CRQQGFGUEAVUIL-UHFFFAOYSA-N 0.000 description 2
JXCGFZXSOMJFOA-UHFFFAOYSA-N chlorotoluron Chemical compound CN(C)C(=O)NC1=CC=C(C)C(Cl)=C1 JXCGFZXSOMJFOA-UHFFFAOYSA-N 0.000 description 2
IVUXTESCPZUGJC-UHFFFAOYSA-N chloroxuron Chemical compound C1=CC(NC(=O)N(C)C)=CC=C1OC1=CC=C(Cl)C=C1 IVUXTESCPZUGJC-UHFFFAOYSA-N 0.000 description 2
KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Natural products OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 2
MZZBPDKVEFVLFF-UHFFFAOYSA-N cyanazine Chemical compound CCNC1=NC(Cl)=NC(NC(C)(C)C#N)=N1 MZZBPDKVEFVLFF-UHFFFAOYSA-N 0.000 description 2
WCMMILVIRZAPLE-UHFFFAOYSA-M cyhexatin Chemical compound C1CCCCC1[Sn](C1CCCCC1)(O)C1CCCCC1 WCMMILVIRZAPLE-UHFFFAOYSA-M 0.000 description 2
QAYICIQNSGETAS-UHFFFAOYSA-N dazomet Chemical compound CN1CSC(=S)N(C)C1 QAYICIQNSGETAS-UHFFFAOYSA-N 0.000 description 2
IWEDIXLBFLAXBO-UHFFFAOYSA-N dicamba Chemical compound COC1=C(Cl)C=CC(Cl)=C1C(O)=O IWEDIXLBFLAXBO-UHFFFAOYSA-N 0.000 description 2
BIXZHMJUSMUDOQ-UHFFFAOYSA-N dichloran Chemical compound NC1=C(Cl)C=C([N+]([O-])=O)C=C1Cl BIXZHMJUSMUDOQ-UHFFFAOYSA-N 0.000 description 2
125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 2
230000000694 effects Effects 0.000 description 2
238000005516 engineering process Methods 0.000 description 2
125000000031 ethylamino group Chemical group [H]C([H])([H])C([H])([H])N([H])[*] 0.000 description 2
238000001125 extrusion Methods 0.000 description 2
239000003337 fertilizer Substances 0.000 description 2
239000012530 fluid Substances 0.000 description 2
125000004216 fluoromethyl group Chemical group [H]C([H])(F)* 0.000 description 2
239000007789 gas Substances 0.000 description 2
239000011521 glass Substances 0.000 description 2
XDDAORKBJWWYJS-UHFFFAOYSA-N glyphosate Chemical compound OC(=O)CNCP(O)(O)=O XDDAORKBJWWYJS-UHFFFAOYSA-N 0.000 description 2
150000004677 hydrates Chemical class 0.000 description 2
239000011777 magnesium Substances 0.000 description 2
229910052749 magnesium Inorganic materials 0.000 description 2
229910052943 magnesium sulfate Inorganic materials 0.000 description 2
UFEJKYYYVXYMMS-UHFFFAOYSA-N methylcarbamic acid Chemical compound CNC(O)=O UFEJKYYYVXYMMS-UHFFFAOYSA-N 0.000 description 2
239000008108 microcrystalline cellulose Substances 0.000 description 2
235000019813 microcrystalline cellulose Nutrition 0.000 description 2
229940016286 microcrystalline cellulose Drugs 0.000 description 2
UNAHYJYOSSSJHH-UHFFFAOYSA-N oryzalin Chemical compound CCCN(CCC)C1=C([N+]([O-])=O)C=C(S(N)(=O)=O)C=C1[N+]([O-])=O UNAHYJYOSSSJHH-UHFFFAOYSA-N 0.000 description 2
125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 description 2
125000003170 phenylsulfonyl group Chemical group C1(=CC=CC=C1)S(=O)(=O)* 0.000 description 2
239000000843 powder Substances 0.000 description 2
230000002028 premature Effects 0.000 description 2
WJNRPILHGGKWCK-UHFFFAOYSA-N propazine Chemical compound CC(C)NC1=NC(Cl)=NC(NC(C)C)=N1 WJNRPILHGGKWCK-UHFFFAOYSA-N 0.000 description 2
150000003839 salts Chemical class 0.000 description 2
238000010008 shearing Methods 0.000 description 2
229940087562 sodium acetate trihydrate Drugs 0.000 description 2
NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 2
229910052911 sodium silicate Inorganic materials 0.000 description 2
238000003860 storage Methods 0.000 description 2
BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 2
YROXIXLRRCOBKF-UHFFFAOYSA-N sulfonylurea Chemical class OC(=N)N=S(=O)=O YROXIXLRRCOBKF-UHFFFAOYSA-N 0.000 description 2
239000004094 surface-active agent Substances 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
229960002447 thiram Drugs 0.000 description 2
REEQLXCGVXDJSQ-UHFFFAOYSA-N trichlopyr Chemical compound OC(=O)COC1=NC(Cl)=C(Cl)C=C1Cl REEQLXCGVXDJSQ-UHFFFAOYSA-N 0.000 description 2
GPRLSGONYQIRFK-MNYXATJNSA-N triton Chemical compound [3H+] GPRLSGONYQIRFK-MNYXATJNSA-N 0.000 description 2
239000004562 water dispersible granule Substances 0.000 description 2
NWONKYPBYAMBJT-UHFFFAOYSA-L zinc sulfate Chemical class [Zn+2].[O-]S([O-])(=O)=O NWONKYPBYAMBJT-UHFFFAOYSA-L 0.000 description 2
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 description 1
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 description 1
IMLJLCJZQLGHJS-JEKSYDDFSA-N (4s,4ar,5s,5ar,6s,12ar)-4-(dimethylamino)-1,5,6,10,11,12a-hexahydroxy-6-methyl-3,12-dioxo-4,4a,5,5a-tetrahydrotetracene-2-carboxamide;dihydrate Chemical compound O.O.C1=CC=C2[C@](O)(C)[C@H]3[C@H](O)[C@H]4[C@H](N(C)C)C(=O)C(C(N)=O)=C(O)[C@@]4(O)C(=O)C3=C(O)C2=C1O IMLJLCJZQLGHJS-JEKSYDDFSA-N 0.000 description 1
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 description 1
AAILEWXSEQLMNI-UHFFFAOYSA-N 1h-pyridazin-6-one Chemical compound OC1=CC=CN=N1 AAILEWXSEQLMNI-UHFFFAOYSA-N 0.000 description 1
MZCNLDQDWLKDNT-UHFFFAOYSA-N 2,3-dihydro-1,2,3-benzothiadiazin-4-one Chemical compound C1=CC=C2C(=O)NNSC2=C1 MZCNLDQDWLKDNT-UHFFFAOYSA-N 0.000 description 1
OVSKIKFHRZPJSS-UHFFFAOYSA-N 2,4-D Chemical compound OC(=O)COC1=CC=C(Cl)C=C1Cl OVSKIKFHRZPJSS-UHFFFAOYSA-N 0.000 description 1
239000002794 2,4-DB Substances 0.000 description 1
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 1
UWHURBUBIHUHSU-UHFFFAOYSA-N 2-[(4-methoxy-6-methyl-1,3,5-triazin-2-yl)carbamoylsulfamoyl]benzoic acid Chemical compound COC1=NC(C)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2)C(O)=O)=N1 UWHURBUBIHUHSU-UHFFFAOYSA-N 0.000 description 1
CABMTIJINOIHOD-UHFFFAOYSA-N 2-[4-methyl-5-oxo-4-(propan-2-yl)-4,5-dihydro-1H-imidazol-2-yl]quinoline-3-carboxylic acid Chemical compound N1C(=O)C(C(C)C)(C)N=C1C1=NC2=CC=CC=C2C=C1C(O)=O CABMTIJINOIHOD-UHFFFAOYSA-N 0.000 description 1
PJXOQDDYIQZWMD-UHFFFAOYSA-N 2-methyl-1-benzofuran-7-ol Chemical compound C1=CC(O)=C2OC(C)=CC2=C1 PJXOQDDYIQZWMD-UHFFFAOYSA-N 0.000 description 1
MDIQXIJPQWLFSD-UHFFFAOYSA-N 3-(2,2-dibromoethenyl)-2,2-dimethylcyclopropane-1-carboxylic acid Chemical compound CC1(C)C(C=C(Br)Br)C1C(O)=O MDIQXIJPQWLFSD-UHFFFAOYSA-N 0.000 description 1
UUXRXRHXOZHHJV-UHFFFAOYSA-N 4,4-dimethyl-1,2-oxazolidin-3-one Chemical compound CC1(C)CONC1=O UUXRXRHXOZHHJV-UHFFFAOYSA-N 0.000 description 1
CDIJOYCNNFLOAX-UHFFFAOYSA-N 4-(trichloromethylsulfanyl)isoindole-1,3-dione Chemical compound ClC(Cl)(Cl)SC1=CC=CC2=C1C(=O)NC2=O CDIJOYCNNFLOAX-UHFFFAOYSA-N 0.000 description 1
JXHFLQSSXXIMGS-UHFFFAOYSA-N 4-hydroxy-3,5-diiodobenzonitrile Chemical compound OC1=C(I)C=C(C#N)C=C1I.OC1=C(I)C=C(C#N)C=C1I.OC1=C(I)C=C(C#N)C=C1I JXHFLQSSXXIMGS-UHFFFAOYSA-N 0.000 description 1
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VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
229910000385 transition metal sulfate Inorganic materials 0.000 description 1
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 description 1
XOPFESVZMSQIKC-UHFFFAOYSA-N triasulfuron Chemical compound COC1=NC(C)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2)OCCCl)=N1 XOPFESVZMSQIKC-UHFFFAOYSA-N 0.000 description 1
229940055764 triaz Drugs 0.000 description 1
229920002554 vinyl polymer Polymers 0.000 description 1
239000012873 virucide Substances 0.000 description 1
239000003232 water-soluble binding agent Substances 0.000 description 1
239000000080 wetting agent Substances 0.000 description 1
229910052725 zinc Inorganic materials 0.000 description 1
239000011701 zinc Substances 0.000 description 1
229910000368 zinc sulfate Inorganic materials 0.000 description 1
239000011686 zinc sulphate Substances 0.000 description 1
235000009529 zinc sulphate Nutrition 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
- A01N25/12—Powders or granules
- A01N25/14—Powders or granules wettable
- 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
- A01N25/12—Powders or granules

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)
Agricultural Chemicals And Associated Chemicals (AREA)

IL9749891A 1990-03-12 1991-03-11 Pesticidal compositions comprising water-soluble heat-activated binder IL97498A (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US49158490A	1990-03-12	1990-03-12

Publications (2)

Publication Number	Publication Date
IL97498A0 IL97498A0 (en)	1992-06-21
IL97498A true IL97498A (en)	1995-07-31

Family

ID=23952839

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
IL9749891A IL97498A (en)	1990-03-12	1991-03-11	Pesticidal compositions comprising water-soluble heat-activated binder

Country Status (23)

Country	Link
US (1)	US5372989A (es)
EP (1)	EP0519937B1 (es)
JP (1)	JPH05504964A (es)
CN (1)	CN1055461A (es)
AT (1)	ATE116099T1 (es)
AU (1)	AU651335B2 (es)
BR (1)	BR9106147A (es)
CA (1)	CA2083185A1 (es)
CS (1)	CS64091A2 (es)
DE (1)	DE69106349T2 (es)
ES (1)	ES2065680T3 (es)
GE (1)	GEP19970938B (es)
HU (1)	HU210697B (es)
IE (1)	IE73214B1 (es)
IL (1)	IL97498A (es)
LT (1)	LT3306B (es)
LV (1)	LV10358B (es)
NZ (1)	NZ237388A (es)
PL (1)	PL167613B1 (es)
PT (1)	PT97010B (es)
TR (1)	TR27589A (es)
WO (1)	WO1991013546A1 (es)
ZA (1)	ZA911811B (es)

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EP0008083A1 (de) *	1978-08-15	1980-02-20	Ciba-Geigy Ag	Verfahren zur Herstellung von Granulaten schwerschmelzbarer Zusatzstoffe für Kunststoffe, insbesondere von Pigmenten, durch thermische Rollgranulierung und die so erhaltenen Granulate
JPS59156422A (ja) *	1983-02-28	1984-09-05	Mitsui Miike Kakoki Kk	造粒方法
CH658066A5 (de) *	1984-03-15	1986-10-15	Ciba Geigy Ag	Verfahren zur herstellung von granulaten wasserloeslicher farbstoffe.
US4558040A (en) *	1984-12-03	1985-12-10	Shell Oil Company	Miticidal (2-alkyl-3,4-dihydro-2H-1-benzopyran-8-yl)-diazenecarboxylic acid esters
CH663622A5 (en) *	1985-02-15	1987-12-31	Ciba Geigy Ag	Process for preparing dye granules
FR2581323B1 (fr) *	1985-05-06	1987-05-29	Rhone Poulenc Spec Chim	Nouvelle composition tensio-active, son procede d'obtention et ses applications
US4931080A (en) *	1985-05-29	1990-06-05	Chan Jimmy H	Solid, phytoactive compositions, methods of use and methods of preparation
FI86501C (fi) *	1985-05-29	1992-09-10	Stauffer Chemical Co	Fast, i huvudsak icke-hygroskopisk fytoaktiv blandning och dess framstaellningsfoerfarande.
US4767557A (en) *	1985-06-28	1988-08-30	The Procter & Gamble Company	Dry bleach and stable enzyme granular composition
US4707287A (en) *	1985-06-28	1987-11-17	The Procter & Gamble Company	Dry bleach stable enzyme composition
US4686209A (en) *	1986-01-10	1987-08-11	E. I. Du Pont De Nemours And Company	Certain N-(substituted-aminosulfinyl)phosphonamidothioate and dithioate pesticides
US4936901A (en) *	1986-07-09	1990-06-26	Monsanto Company	Formulations of water-dispersible granules and process for preparation thereof
DK170456B1 (da) *	1986-08-18	1995-09-11	Stauffer Chemical Co	Fremgangsmåde til fremstilling af faste, fytoaktive midler
JP2770400B2 (ja) *	1989-04-18	1998-07-02	住友化学工業株式会社	農薬固型製剤

1991
- 1991-02-27 CA CA002083185A patent/CA2083185A1/en not_active Abandoned
- 1991-02-27 HU HU9202911A patent/HU210697B/hu not_active IP Right Cessation
- 1991-02-27 AT AT91904761T patent/ATE116099T1/de not_active IP Right Cessation
- 1991-02-27 PL PL91293187A patent/PL167613B1/pl unknown
- 1991-02-27 DE DE69106349T patent/DE69106349T2/de not_active Expired - Fee Related
- 1991-02-27 EP EP91904761A patent/EP0519937B1/en not_active Expired - Lifetime
- 1991-02-27 JP JP3505578A patent/JPH05504964A/ja active Pending
- 1991-02-27 WO PCT/US1991/001105 patent/WO1991013546A1/en not_active Ceased
- 1991-02-27 AU AU73325/91A patent/AU651335B2/en not_active Ceased
- 1991-02-27 ES ES91904761T patent/ES2065680T3/es not_active Expired - Lifetime
- 1991-02-27 US US07/934,467 patent/US5372989A/en not_active Expired - Fee Related
- 1991-02-27 BR BR919106147A patent/BR9106147A/pt not_active Application Discontinuation
- 1991-03-08 TR TR00240/91A patent/TR27589A/xx unknown
- 1991-03-11 NZ NZ237388A patent/NZ237388A/en unknown
- 1991-03-11 IE IE78991A patent/IE73214B1/en not_active IP Right Cessation
- 1991-03-11 PT PT97010A patent/PT97010B/pt not_active IP Right Cessation
- 1991-03-11 IL IL9749891A patent/IL97498A/en unknown
- 1991-03-12 ZA ZA911811A patent/ZA911811B/xx unknown
- 1991-03-12 CN CN91101964A patent/CN1055461A/zh active Pending
- 1991-03-12 CS CS91640A patent/CS64091A2/cs unknown
1993
- 1993-03-18 LT LTIP428A patent/LT3306B/lt not_active IP Right Cessation
- 1993-05-12 LV LVP-93-326A patent/LV10358B/en unknown
- 1993-07-15 GE GEAP19931025A patent/GEP19970938B/en unknown

Also Published As

Publication number	Publication date
PL167613B1 (pl)	1995-09-30
IL97498A0 (en)	1992-06-21
HU210697B (en)	1995-06-28
WO1991013546A1 (en)	1991-09-19
ES2065680T3 (es)	1995-02-16
IE910789A1 (en)	1991-09-25
BR9106147A (pt)	1993-03-09
DE69106349T2 (de)	1995-06-01
TR27589A (tr)	1995-06-13
ZA911811B (en)	1992-11-25
PT97010B (pt)	1998-07-31
AU651335B2 (en)	1994-07-21
LT3306B (en)	1995-06-26
EP0519937B1 (en)	1994-12-28
GEP19970938B (en)	1997-04-06
LTIP428A (en)	1994-10-25
CA2083185A1 (en)	1991-09-13
LV10358B (en)	1996-02-20
AU7332591A (en)	1991-10-10
PL293187A1 (en)	1992-10-05
LV10358A (lv)	1995-02-20
NZ237388A (en)	1993-04-28
IE73214B1 (en)	1997-05-07
CN1055461A (zh)	1991-10-23
US5372989A (en)	1994-12-13
ATE116099T1 (de)	1995-01-15
PT97010A (pt)	1991-12-31
EP0519937A1 (en)	1992-12-30
DE69106349D1 (de)	1995-02-09
JPH05504964A (ja)	1993-07-29
HUT61646A (en)	1993-03-01
HU9202911D0 (en)	1992-11-30
CS64091A2 (en)	1991-10-15

Legal Events

Date	Code	Title	Description
1997-06-10	KB	Patent renewed

Publication	Publication Date	Title
US5372989A (en)	1994-12-13	Water-dispersible or water-soluble pesticide grandules from heat-activated binders
US5474971A (en)	1995-12-12	Water-dispersible granular agricultural compositions made by heat extrusion
AU2007230693B2 (en)	2013-02-14	Granular formulation
CA1337458C (en)	1995-10-31	Tablet formulations of pesticides
AU633848B2 (en)	1993-02-11	Water-soluble or water-dispersible pesticide granules
JP2004352711A (ja)	2004-12-16	粒状農薬組成物、その製造方法及び使用方法
US5569639A (en)	1996-10-29	Dry flowable agricultural compositions of glyphosate and sulfonylurea herbicides made without drying of the final product
JP5285074B2 (ja)	2013-09-11	顆粒水和剤
PL172504B1 (pl)	1997-10-31	Sposób wytwarzania granulowanego produktu chwastobójczego PL PL PL
JP5176160B2 (ja)	2013-04-03	農薬粒状組成物
NZ233432A (en)	1991-05-28	Pan-granulating process using steam
JP2003313102A (ja)	2003-11-06	農薬粒状水和剤
KR19990039757A (ko)	1999-06-05	경엽 및 토양처리용 후라자설푸론계 제초입제