EP2106211A2 - Pflanzenschutzgranulate zur applikation auf die blattoberfläche - Google Patents
Pflanzenschutzgranulate zur applikation auf die blattoberflächeInfo
- Publication number
- EP2106211A2 EP2106211A2 EP07846579A EP07846579A EP2106211A2 EP 2106211 A2 EP2106211 A2 EP 2106211A2 EP 07846579 A EP07846579 A EP 07846579A EP 07846579 A EP07846579 A EP 07846579A EP 2106211 A2 EP2106211 A2 EP 2106211A2
- Authority
- EP
- European Patent Office
- Prior art keywords
- granules
- methyl
- oil
- ethyl
- granules according
- 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.)
- Withdrawn
Links
- 239000008187 granular material Substances 0.000 title claims abstract description 110
- 239000000203 mixture Substances 0.000 claims description 22
- 238000000034 method Methods 0.000 claims description 21
- 239000013543 active substance Substances 0.000 claims description 16
- 230000008569 process Effects 0.000 claims description 14
- 230000035515 penetration Effects 0.000 claims description 11
- 239000003205 fragrance Substances 0.000 claims description 10
- 238000010297 mechanical methods and process Methods 0.000 claims description 10
- 239000012868 active agrochemical ingredient Substances 0.000 claims description 9
- 238000009472 formulation Methods 0.000 claims description 9
- 229920002472 Starch Polymers 0.000 claims description 8
- 239000008107 starch Substances 0.000 claims description 8
- 235000019698 starch Nutrition 0.000 claims description 8
- 239000003795 chemical substances by application Substances 0.000 claims description 5
- 229940079593 drug Drugs 0.000 claims description 5
- 239000003814 drug Substances 0.000 claims description 5
- 239000003755 preservative agent Substances 0.000 claims description 5
- 235000013339 cereals Nutrition 0.000 claims description 3
- 239000004606 Fillers/Extenders Substances 0.000 claims description 2
- 239000000470 constituent Substances 0.000 claims description 2
- 239000000975 dye Substances 0.000 claims description 2
- 239000000945 filler Substances 0.000 claims description 2
- 239000000314 lubricant Substances 0.000 claims description 2
- 239000011814 protection agent Substances 0.000 claims description 2
- 238000004519 manufacturing process Methods 0.000 abstract description 3
- 230000000149 penetrating effect Effects 0.000 abstract 1
- -1 Cyazofamide Chemical compound 0.000 description 61
- 239000003112 inhibitor Substances 0.000 description 21
- 239000003921 oil Substances 0.000 description 19
- 235000019198 oils Nutrition 0.000 description 19
- 150000002148 esters Chemical class 0.000 description 15
- 239000000654 additive Substances 0.000 description 10
- 239000003905 agrochemical Substances 0.000 description 9
- 239000004480 active ingredient Substances 0.000 description 8
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 8
- 239000011734 sodium Substances 0.000 description 7
- 229910052708 sodium Inorganic materials 0.000 description 7
- 241000196324 Embryophyta Species 0.000 description 6
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 6
- 239000000126 substance Substances 0.000 description 6
- 239000007921 spray Substances 0.000 description 5
- GLZPCOQZEFWAFX-UHFFFAOYSA-N Geraniol Chemical compound CC(C)=CCCC(C)=CCO GLZPCOQZEFWAFX-UHFFFAOYSA-N 0.000 description 4
- 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 4
- 239000002253 acid Substances 0.000 description 4
- 239000000853 adhesive Substances 0.000 description 4
- 230000001070 adhesive effect Effects 0.000 description 4
- QUKGYYKBILRGFE-UHFFFAOYSA-N benzyl acetate Chemical compound CC(=O)OCC1=CC=CC=C1 QUKGYYKBILRGFE-UHFFFAOYSA-N 0.000 description 4
- ULDHMXUKGWMISQ-UHFFFAOYSA-N carvone Chemical compound CC(=C)C1CC=C(C)C(=O)C1 ULDHMXUKGWMISQ-UHFFFAOYSA-N 0.000 description 4
- 238000001816 cooling Methods 0.000 description 4
- 235000014113 dietary fatty acids Nutrition 0.000 description 4
- 229930195729 fatty acid Natural products 0.000 description 4
- 239000000194 fatty acid Substances 0.000 description 4
- VAMXMNNIEUEQDV-UHFFFAOYSA-N methyl anthranilate Chemical compound COC(=O)C1=CC=CC=C1N VAMXMNNIEUEQDV-UHFFFAOYSA-N 0.000 description 4
- ZRSNZINYAWTAHE-UHFFFAOYSA-N p-methoxybenzaldehyde Chemical compound COC1=CC=C(C=O)C=C1 ZRSNZINYAWTAHE-UHFFFAOYSA-N 0.000 description 4
- 239000000575 pesticide Substances 0.000 description 4
- 238000002360 preparation method Methods 0.000 description 4
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 3
- 235000021307 Triticum Nutrition 0.000 description 3
- 244000098338 Triticum aestivum Species 0.000 description 3
- 150000007513 acids Chemical class 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 238000001035 drying Methods 0.000 description 3
- MTZQAGJQAFMTAQ-UHFFFAOYSA-N ethyl benzoate Chemical compound CCOC(=O)C1=CC=CC=C1 MTZQAGJQAFMTAQ-UHFFFAOYSA-N 0.000 description 3
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 3
- 239000003925 fat Substances 0.000 description 3
- NYPJDWWKZLNGGM-UHFFFAOYSA-N fenvalerate Aalpha Natural products C=1C=C(Cl)C=CC=1C(C(C)C)C(=O)OC(C#N)C(C=1)=CC=CC=1OC1=CC=CC=C1 NYPJDWWKZLNGGM-UHFFFAOYSA-N 0.000 description 3
- FOUWCSDKDDHKQP-UHFFFAOYSA-N flumioxazin Chemical compound FC1=CC=2OCC(=O)N(CC#C)C=2C=C1N(C1=O)C(=O)C2=C1CCCC2 FOUWCSDKDDHKQP-UHFFFAOYSA-N 0.000 description 3
- JLYXXMFPNIAWKQ-UHFFFAOYSA-N gamma-hexachlorocyclohexane Natural products ClC1C(Cl)C(Cl)C(Cl)C(Cl)C1Cl JLYXXMFPNIAWKQ-UHFFFAOYSA-N 0.000 description 3
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 3
- KXKVLQRXCPHEJC-UHFFFAOYSA-N methyl acetate Chemical compound COC(C)=O KXKVLQRXCPHEJC-UHFFFAOYSA-N 0.000 description 3
- 230000035806 respiratory chain Effects 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- 238000005204 segregation Methods 0.000 description 3
- 238000003860 storage Methods 0.000 description 3
- OORLZFUTLGXMEF-UHFFFAOYSA-N sulfentrazone Chemical compound O=C1N(C(F)F)C(C)=NN1C1=CC(NS(C)(=O)=O)=C(Cl)C=C1Cl OORLZFUTLGXMEF-UHFFFAOYSA-N 0.000 description 3
- KMPQYAYAQWNLME-UHFFFAOYSA-N undecanal Chemical compound CCCCCCCCCCC=O KMPQYAYAQWNLME-UHFFFAOYSA-N 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- ZCVAOQKBXKSDMS-PVAVHDDUSA-N (+)-trans-(S)-allethrin Chemical compound CC1(C)[C@H](C=C(C)C)[C@H]1C(=O)O[C@@H]1C(C)=C(CC=C)C(=O)C1 ZCVAOQKBXKSDMS-PVAVHDDUSA-N 0.000 description 2
- OOCCDEMITAIZTP-QPJJXVBHSA-N (E)-cinnamyl alcohol Chemical compound OC\C=C\C1=CC=CC=C1 OOCCDEMITAIZTP-QPJJXVBHSA-N 0.000 description 2
- JLIDRDJNLAWIKT-UHFFFAOYSA-N 1,2-dimethyl-3h-benzo[e]indole Chemical compound C1=CC=CC2=C(C(=C(C)N3)C)C3=CC=C21 JLIDRDJNLAWIKT-UHFFFAOYSA-N 0.000 description 2
- DELJNDWGTWHHFA-UHFFFAOYSA-N 1-azaniumylpropyl(hydroxy)phosphinate Chemical compound CCC(N)P(O)(O)=O DELJNDWGTWHHFA-UHFFFAOYSA-N 0.000 description 2
- HMKKIXGYKWDQSV-SDNWHVSQSA-N 2-Pentyl-3-phenyl-2-propenal Chemical compound CCCCC\C(C=O)=C/C1=CC=CC=C1 HMKKIXGYKWDQSV-SDNWHVSQSA-N 0.000 description 2
- QGLVWTFUWVTDEQ-UHFFFAOYSA-N 2-chloro-3-methoxyphenol Chemical compound COC1=CC=CC(O)=C1Cl QGLVWTFUWVTDEQ-UHFFFAOYSA-N 0.000 description 2
- 229940044120 2-n-octyl-4-isothiazolin-3-one Drugs 0.000 description 2
- AVGVFDSUDIUXEU-UHFFFAOYSA-N 2-octyl-1,2-thiazolidin-3-one Chemical compound CCCCCCCCN1SCCC1=O AVGVFDSUDIUXEU-UHFFFAOYSA-N 0.000 description 2
- WRMNZCZEMHIOCP-UHFFFAOYSA-N 2-phenylethanol Chemical compound OCCC1=CC=CC=C1 WRMNZCZEMHIOCP-UHFFFAOYSA-N 0.000 description 2
- GNKZMNRKLCTJAY-UHFFFAOYSA-N 4'-Methylacetophenone Chemical compound CC(=O)C1=CC=C(C)C=C1 GNKZMNRKLCTJAY-UHFFFAOYSA-N 0.000 description 2
- ZXVONLUNISGICL-UHFFFAOYSA-N 4,6-dinitro-o-cresol Chemical compound CC1=CC([N+]([O-])=O)=CC([N+]([O-])=O)=C1O ZXVONLUNISGICL-UHFFFAOYSA-N 0.000 description 2
- PVSGXWMWNRGTKE-UHFFFAOYSA-N 5-methyl-2-[4-methyl-5-oxo-4-(propan-2-yl)-4,5-dihydro-1H-imidazol-2-yl]pyridine-3-carboxylic acid Chemical compound N1C(=O)C(C(C)C)(C)N=C1C1=NC=C(C)C=C1C(O)=O PVSGXWMWNRGTKE-UHFFFAOYSA-N 0.000 description 2
- DVOODWOZJVJKQR-UHFFFAOYSA-N 5-tert-butyl-3-(2,4-dichloro-5-prop-2-ynoxyphenyl)-1,3,4-oxadiazol-2-one Chemical group O=C1OC(C(C)(C)C)=NN1C1=CC(OCC#C)=C(Cl)C=C1Cl DVOODWOZJVJKQR-UHFFFAOYSA-N 0.000 description 2
- VSVKOUBCDZYAQY-UHFFFAOYSA-N 7-chloro-1,2-benzothiazole Chemical compound ClC1=CC=CC2=C1SN=C2 VSVKOUBCDZYAQY-UHFFFAOYSA-N 0.000 description 2
- KWOLFJPFCHCOCG-UHFFFAOYSA-N Acetophenone Chemical compound CC(=O)C1=CC=CC=C1 KWOLFJPFCHCOCG-UHFFFAOYSA-N 0.000 description 2
- 102000012440 Acetylcholinesterase Human genes 0.000 description 2
- 108010022752 Acetylcholinesterase Proteins 0.000 description 2
- MDBGGTQNNUOQRC-UHFFFAOYSA-N Allidochlor Chemical compound ClCC(=O)N(CC=C)CC=C MDBGGTQNNUOQRC-UHFFFAOYSA-N 0.000 description 2
- 239000005885 Buprofezin Substances 0.000 description 2
- ZTQSAGDEMFDKMZ-UHFFFAOYSA-N Butyraldehyde Chemical compound CCCC=O ZTQSAGDEMFDKMZ-UHFFFAOYSA-N 0.000 description 2
- 239000005973 Carvone Substances 0.000 description 2
- 239000005494 Chlorotoluron Substances 0.000 description 2
- 108010009685 Cholinergic Receptors Proteins 0.000 description 2
- MDNWOSOZYLHTCG-UHFFFAOYSA-N Dichlorophen Chemical compound OC1=CC=C(Cl)C=C1CC1=CC(Cl)=CC=C1O MDNWOSOZYLHTCG-UHFFFAOYSA-N 0.000 description 2
- LBGPXIPGGRQBJW-UHFFFAOYSA-N Difenzoquat Chemical compound C[N+]=1N(C)C(C=2C=CC=CC=2)=CC=1C1=CC=CC=C1 LBGPXIPGGRQBJW-UHFFFAOYSA-N 0.000 description 2
- FHUODBDRWMIBQP-UHFFFAOYSA-N Ethyl p-anisate Chemical compound CCOC(=O)C1=CC=C(OC)C=C1 FHUODBDRWMIBQP-UHFFFAOYSA-N 0.000 description 2
- FDNBWBAHQKZDSN-UHFFFAOYSA-N F5231 Chemical compound C1=C(Cl)C(NS(=O)(=O)CC)=CC(N2C(N(CCCF)N=N2)=O)=C1F FDNBWBAHQKZDSN-UHFFFAOYSA-N 0.000 description 2
- AOQMRUTZEYVDIL-UHFFFAOYSA-N Flupoxam Chemical compound C=1C=C(Cl)C(COCC(F)(F)C(F)(F)F)=CC=1N1N=C(C(=O)N)N=C1C1=CC=CC=C1 AOQMRUTZEYVDIL-UHFFFAOYSA-N 0.000 description 2
- AMIMRNSIRUDHCM-UHFFFAOYSA-N Isopropylaldehyde Chemical compound CC(C)C=O AMIMRNSIRUDHCM-UHFFFAOYSA-N 0.000 description 2
- CRZQGDNQQAALAY-UHFFFAOYSA-N Methyl benzeneacetate Chemical compound COC(=O)CC1=CC=CC=C1 CRZQGDNQQAALAY-UHFFFAOYSA-N 0.000 description 2
- LGDSHSYDSCRFAB-UHFFFAOYSA-N Methyl isothiocyanate Chemical compound CN=C=S LGDSHSYDSCRFAB-UHFFFAOYSA-N 0.000 description 2
- ZYEMGPIYFIJGTP-UHFFFAOYSA-N O-methyleugenol Chemical compound COC1=CC=C(CC=C)C=C1OC ZYEMGPIYFIJGTP-UHFFFAOYSA-N 0.000 description 2
- LTUNNEGNEKBSEH-UHFFFAOYSA-N Prosulfuron Chemical compound COC1=NC(C)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2)CCC(F)(F)F)=N1 LTUNNEGNEKBSEH-UHFFFAOYSA-N 0.000 description 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
- 239000005616 Rimsulfuron Substances 0.000 description 2
- 244000028419 Styrax benzoin Species 0.000 description 2
- 235000000126 Styrax benzoin Nutrition 0.000 description 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 2
- PNRAZZZISDRWMV-UHFFFAOYSA-N Terbucarb Chemical compound CNC(=O)OC1=C(C(C)(C)C)C=C(C)C=C1C(C)(C)C PNRAZZZISDRWMV-UHFFFAOYSA-N 0.000 description 2
- YIJZJEYQBAAWRJ-UHFFFAOYSA-N Thiazopyr Chemical compound N1=C(C(F)F)C(C(=O)OC)=C(CC(C)C)C(C=2SCCN=2)=C1C(F)(F)F YIJZJEYQBAAWRJ-UHFFFAOYSA-N 0.000 description 2
- FSAVDKDHPDSCTO-WQLSENKSSA-N [(z)-2-chloro-1-(2,4-dichlorophenyl)ethenyl] diethyl phosphate Chemical compound CCOP(=O)(OCC)O\C(=C/Cl)C1=CC=C(Cl)C=C1Cl FSAVDKDHPDSCTO-WQLSENKSSA-N 0.000 description 2
- 102000034337 acetylcholine receptors Human genes 0.000 description 2
- 229940022698 acetylcholinesterase Drugs 0.000 description 2
- 239000000556 agonist Substances 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- 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 description 2
- RDOXTESZEPMUJZ-UHFFFAOYSA-N anisole Chemical compound COC1=CC=CC=C1 RDOXTESZEPMUJZ-UHFFFAOYSA-N 0.000 description 2
- MAHPNPYYQAIOJN-UHFFFAOYSA-N azimsulfuron Chemical compound COC1=CC(OC)=NC(NC(=O)NS(=O)(=O)C=2N(N=CC=2C2=NN(C)N=N2)C)=N1 MAHPNPYYQAIOJN-UHFFFAOYSA-N 0.000 description 2
- HUMNYLRZRPPJDN-UHFFFAOYSA-N benzaldehyde Chemical compound O=CC1=CC=CC=C1 HUMNYLRZRPPJDN-UHFFFAOYSA-N 0.000 description 2
- DULCUDSUACXJJC-UHFFFAOYSA-N benzeneacetic acid ethyl ester Natural products CCOC(=O)CC1=CC=CC=C1 DULCUDSUACXJJC-UHFFFAOYSA-N 0.000 description 2
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 2
- ISAOCJYIOMOJEB-UHFFFAOYSA-N benzoin Chemical compound C=1C=CC=CC=1C(O)C(=O)C1=CC=CC=C1 ISAOCJYIOMOJEB-UHFFFAOYSA-N 0.000 description 2
- 229940007550 benzyl acetate Drugs 0.000 description 2
- GINJFDRNADDBIN-FXQIFTODSA-N bilanafos Chemical compound OC(=O)[C@H](C)NC(=O)[C@H](C)NC(=O)[C@@H](N)CCP(C)(O)=O GINJFDRNADDBIN-FXQIFTODSA-N 0.000 description 2
- 229960001901 bioallethrin Drugs 0.000 description 2
- 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 2
- LLEMOWNGBBNAJR-UHFFFAOYSA-N biphenyl-2-ol Chemical compound OC1=CC=CC=C1C1=CC=CC=C1 LLEMOWNGBBNAJR-UHFFFAOYSA-N 0.000 description 2
- FUHMZYWBSHTEDZ-UHFFFAOYSA-M bispyribac-sodium Chemical compound [Na+].COC1=CC(OC)=NC(OC=2C(=C(OC=3N=C(OC)C=C(OC)N=3)C=CC=2)C([O-])=O)=N1 FUHMZYWBSHTEDZ-UHFFFAOYSA-M 0.000 description 2
- PRLVTUNWOQKEAI-VKAVYKQESA-N buprofezin Chemical compound O=C1N(C(C)C)\C(=N\C(C)(C)C)SCN1C1=CC=CC=C1 PRLVTUNWOQKEAI-VKAVYKQESA-N 0.000 description 2
- XUPYJHCZDLZNFP-UHFFFAOYSA-N butyl butanoate Chemical compound CCCCOC(=O)CCC XUPYJHCZDLZNFP-UHFFFAOYSA-N 0.000 description 2
- KXRPCFINVWWFHQ-UHFFFAOYSA-N cadusafos Chemical compound CCC(C)SP(=O)(OCC)SC(C)CC KXRPCFINVWWFHQ-UHFFFAOYSA-N 0.000 description 2
- GYSSRZJIHXQEHQ-UHFFFAOYSA-N carboxin Chemical compound S1CCOC(C)=C1C(=O)NC1=CC=CC=C1 GYSSRZJIHXQEHQ-UHFFFAOYSA-N 0.000 description 2
- HQKQRXZEXPXXIG-VJOHVRBBSA-N chembl2333940 Chemical compound C1[C@]23[C@H](C)CC[C@H]3C(C)(C)[C@H]1[C@@](OC(C)=O)(C)CC2 HQKQRXZEXPXXIG-VJOHVRBBSA-N 0.000 description 2
- PSOVNZZNOMJUBI-UHFFFAOYSA-N chlorantraniliprole Chemical compound CNC(=O)C1=CC(Cl)=CC(C)=C1NC(=O)C1=CC(Br)=NN1C1=NC=CC=C1Cl PSOVNZZNOMJUBI-UHFFFAOYSA-N 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
- LFHISGNCFUNFFM-UHFFFAOYSA-N chloropicrin Chemical compound [O-][N+](=O)C(Cl)(Cl)Cl LFHISGNCFUNFFM-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
- NEHNMFOYXAPHSD-UHFFFAOYSA-N citronellal Chemical compound O=CCC(C)CCC=C(C)C NEHNMFOYXAPHSD-UHFFFAOYSA-N 0.000 description 2
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- JOZKFWLRHCDGJA-UHFFFAOYSA-N citronellol acetate Chemical compound CC(=O)OCCC(C)CCC=C(C)C JOZKFWLRHCDGJA-UHFFFAOYSA-N 0.000 description 2
- KIEDNEWSYUYDSN-UHFFFAOYSA-N clomazone Chemical compound O=C1C(C)(C)CON1CC1=CC=CC=C1Cl KIEDNEWSYUYDSN-UHFFFAOYSA-N 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 230000003750 conditioning effect Effects 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- 229910000365 copper sulfate Inorganic materials 0.000 description 2
- ARUVKPQLZAKDPS-UHFFFAOYSA-L copper(II) sulfate Chemical compound [Cu+2].[O-][S+2]([O-])([O-])[O-] ARUVKPQLZAKDPS-UHFFFAOYSA-L 0.000 description 2
- WTWBUQJHJGUZCY-UHFFFAOYSA-N cuminaldehyde Chemical compound CC(C)C1=CC=C(C=O)C=C1 WTWBUQJHJGUZCY-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
- KAATUXNTWXVJKI-UHFFFAOYSA-N cypermethrin Chemical compound CC1(C)C(C=C(Cl)Cl)C1C(=O)OC(C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 KAATUXNTWXVJKI-UHFFFAOYSA-N 0.000 description 2
- KSMVZQYAVGTKIV-UHFFFAOYSA-N decanal Chemical compound CCCCCCCCCC=O KSMVZQYAVGTKIV-UHFFFAOYSA-N 0.000 description 2
- 229960003887 dichlorophen Drugs 0.000 description 2
- OEBRKCOSUFCWJD-UHFFFAOYSA-N dichlorvos Chemical compound COP(=O)(OC)OC=C(Cl)Cl OEBRKCOSUFCWJD-UHFFFAOYSA-N 0.000 description 2
- 150000005690 diesters Chemical class 0.000 description 2
- 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 2
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical compound C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 2
- USIUVYZYUHIAEV-UHFFFAOYSA-N diphenyl ether Chemical compound C=1C=CC=CC=1OC1=CC=CC=C1 USIUVYZYUHIAEV-UHFFFAOYSA-N 0.000 description 2
- DMBHHRLKUKUOEG-UHFFFAOYSA-N diphenylamine Chemical compound C=1C=CC=CC=1NC1=CC=CC=C1 DMBHHRLKUKUOEG-UHFFFAOYSA-N 0.000 description 2
- LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 description 2
- 239000000428 dust Substances 0.000 description 2
- CXEGAUYXQAKHKJ-NSBHKLITSA-N emamectin B1a Chemical compound C1=C[C@H](C)[C@@H]([C@@H](C)CC)O[C@]11O[C@H](C\C=C(C)\[C@@H](O[C@@H]2O[C@@H](C)[C@H](O[C@@H]3O[C@@H](C)[C@H](NC)[C@@H](OC)C3)[C@@H](OC)C2)[C@@H](C)\C=C\C=C/2[C@]3([C@H](C(=O)O4)C=C(C)[C@@H](O)[C@H]3OC\2)O)C[C@H]4C1 CXEGAUYXQAKHKJ-NSBHKLITSA-N 0.000 description 2
- 239000003623 enhancer Substances 0.000 description 2
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- 150000003871 sulfonates Chemical class 0.000 description 1
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- DQFPEYARZIQXRM-LTGZKZEYSA-N tralkoxydim Chemical compound C1C(=O)C(C(/CC)=N/OCC)=C(O)CC1C1=C(C)C=C(C)C=C1C DQFPEYARZIQXRM-LTGZKZEYSA-N 0.000 description 1
- YWSCPYYRJXKUDB-KAKFPZCNSA-N tralomethrin Chemical compound CC1(C)[C@@H](C(Br)C(Br)(Br)Br)[C@H]1C(=O)O[C@H](C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 YWSCPYYRJXKUDB-KAKFPZCNSA-N 0.000 description 1
- BJIOGJUNALELMI-UHFFFAOYSA-N trans-isoeugenol Natural products COC1=CC(C=CC)=CC=C1O BJIOGJUNALELMI-UHFFFAOYSA-N 0.000 description 1
- DDVNRFNDOPPVQJ-HQJQHLMTSA-N transfluthrin Chemical compound CC1(C)[C@H](C=C(Cl)Cl)[C@H]1C(=O)OCC1=C(F)C(F)=CC(F)=C1F DDVNRFNDOPPVQJ-HQJQHLMTSA-N 0.000 description 1
- 230000014616 translation Effects 0.000 description 1
- 150000003626 triacylglycerols Chemical class 0.000 description 1
- JWXZLCFGVKMEEK-UHFFFAOYSA-N triarathene Chemical compound C1=CC(Cl)=CC=C1C1=CC(C=2C=CC=CC=2)=C(C=2C=CC=CC=2)S1 JWXZLCFGVKMEEK-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
- AMFGTOFWMRQMEM-UHFFFAOYSA-N triazophos Chemical compound N1=C(OP(=S)(OCC)OCC)N=CN1C1=CC=CC=C1 AMFGTOFWMRQMEM-UHFFFAOYSA-N 0.000 description 1
- IQGKIPDJXCAMSM-UHFFFAOYSA-N triazoxide Chemical compound N=1C2=CC=C(Cl)C=C2[N+]([O-])=NC=1N1C=CN=C1 IQGKIPDJXCAMSM-UHFFFAOYSA-N 0.000 description 1
- BQZXUHDXIARLEO-UHFFFAOYSA-N tribenuron Chemical compound COC1=NC(C)=NC(N(C)C(=O)NS(=O)(=O)C=2C(=CC=CC=2)C(O)=O)=N1 BQZXUHDXIARLEO-UHFFFAOYSA-N 0.000 description 1
- REEQLXCGVXDJSQ-UHFFFAOYSA-N trichlopyr Chemical compound OC(=O)COC1=NC(Cl)=C(Cl)C=C1Cl REEQLXCGVXDJSQ-UHFFFAOYSA-N 0.000 description 1
- NFACJZMKEDPNKN-UHFFFAOYSA-N trichlorfon Chemical compound COP(=O)(OC)C(O)C(Cl)(Cl)Cl NFACJZMKEDPNKN-UHFFFAOYSA-N 0.000 description 1
- DQJCHOQLCLEDLL-UHFFFAOYSA-N tricyclazole Chemical compound CC1=CC=CC2=C1N1C=NN=C1S2 DQJCHOQLCLEDLL-UHFFFAOYSA-N 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
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- 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 1
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- IMEVJVISCHQJRM-UHFFFAOYSA-N triflusulfuron-methyl Chemical compound COC(=O)C1=CC=CC(C)=C1S(=O)(=O)NC(=O)NC1=NC(OCC(F)(F)F)=NC(N(C)C)=N1 IMEVJVISCHQJRM-UHFFFAOYSA-N 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
- 125000000026 trimethylsilyl group Chemical group [H]C([H])([H])[Si]([*])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- KVEQCVKVIFQSGC-UHFFFAOYSA-N tritosulfuron Chemical compound FC(F)(F)C1=NC(OC)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2)C(F)(F)F)=N1 KVEQCVKVIFQSGC-UHFFFAOYSA-N 0.000 description 1
- KYWIYKKSMDLRDC-UHFFFAOYSA-N undecan-2-one Chemical compound CCCCCCCCCC(C)=O KYWIYKKSMDLRDC-UHFFFAOYSA-N 0.000 description 1
- 238000011144 upstream manufacturing Methods 0.000 description 1
- 229940070710 valerate Drugs 0.000 description 1
- NQPDZGIKBAWPEJ-UHFFFAOYSA-N valeric acid Chemical compound CCCCC(O)=O NQPDZGIKBAWPEJ-UHFFFAOYSA-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
- DBXFMOWZRXXBRN-LWKPJOBUSA-N valifenalate Chemical compound CC(C)OC(=O)N[C@@H](C(C)C)C(=O)NC(CC(=O)OC)C1=CC=C(Cl)C=C1 DBXFMOWZRXXBRN-LWKPJOBUSA-N 0.000 description 1
- LESVOLZBIFDZGS-UHFFFAOYSA-N vamidothion Chemical compound CNC(=O)C(C)SCCSP(=O)(OC)OC LESVOLZBIFDZGS-UHFFFAOYSA-N 0.000 description 1
- MWOOGOJBHIARFG-UHFFFAOYSA-N vanillin Chemical compound COC1=CC(C=O)=CC=C1O MWOOGOJBHIARFG-UHFFFAOYSA-N 0.000 description 1
- FGQOOHJZONJGDT-UHFFFAOYSA-N vanillin Natural products COC1=CC(O)=CC(C=O)=C1 FGQOOHJZONJGDT-UHFFFAOYSA-N 0.000 description 1
- 235000012141 vanillin Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 239000010679 vetiver oil Substances 0.000 description 1
- BCEHBSKCWLPMDN-MGPLVRAMSA-N voriconazole Chemical compound C1([C@H](C)[C@](O)(CN2N=CN=C2)C=2C(=CC(F)=CC=2)F)=NC=NC=C1F BCEHBSKCWLPMDN-MGPLVRAMSA-N 0.000 description 1
- 229960004740 voriconazole Drugs 0.000 description 1
- ZFNVDHOSLNRHNN-UHFFFAOYSA-N xi-3-(4-Isopropylphenyl)-2-methylpropanal Chemical compound O=CC(C)CC1=CC=C(C(C)C)C=C1 ZFNVDHOSLNRHNN-UHFFFAOYSA-N 0.000 description 1
- WCJYTPVNMWIZCG-UHFFFAOYSA-N xylylcarb Chemical compound CNC(=O)OC1=CC=C(C)C(C)=C1 WCJYTPVNMWIZCG-UHFFFAOYSA-N 0.000 description 1
- AMHNZOICSMBGDH-UHFFFAOYSA-L zineb Chemical compound [Zn+2].[S-]C(=S)NCCNC([S-])=S AMHNZOICSMBGDH-UHFFFAOYSA-L 0.000 description 1
- DUBNHZYBDBBJHD-UHFFFAOYSA-L ziram Chemical compound [Zn+2].CN(C)C([S-])=S.CN(C)C([S-])=S DUBNHZYBDBBJHD-UHFFFAOYSA-L 0.000 description 1
- FJBGIXKIXPUXBY-UHFFFAOYSA-N {2-[3-(4-chlorophenyl)propyl]-2,4,4-trimethyl-1,3-oxazolidin-3-yl}(imidazol-1-yl)methanone Chemical compound C1=CN=CN1C(=O)N1C(C)(C)COC1(C)CCCC1=CC=C(Cl)C=C1 FJBGIXKIXPUXBY-UHFFFAOYSA-N 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
-
- 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
- A01N25/24—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 ingredients to enhance the sticking of the active ingredients
-
- 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
- A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
- A01N43/74—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms five-membered rings with one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,3
- A01N43/76—1,3-Oxazoles; Hydrogenated 1,3-oxazoles
Definitions
- the present invention relates to granules for application to the leaf surface, and to a process for its preparation. Another object of the present invention is the use of this granules for sheet penetration or bait formulation.
- Plant protection products are usually applied as spray mixtures, i. the drug formulation is sprayed as a liquid system or as a spray on the leaf surfaces of plants.
- the handling of spray mixtures is complex, requires special equipment and is not pleasant for the user.
- the pesticides should preferably be applied in the form of granules in order to simultaneously achieve better public acceptance for the use of pesticides.
- Agrochemical granules also have the advantage that they can be easily perceived after the discharge of the granules, so that it can be seen whether a field has been treated or not. Moreover, the use of granules comprising agrochemical agents is simpler than the use of appropriate aqueous or emulsion containing solutions.
- the object of the present invention was accordingly to provide pesticides in the form of granules which can be applied directly to the leaf surface of plants, where they preferably adhere and preferably deliver there the active ingredient to the plant.
- This object is achieved by a granulate containing at least one agrochemical active ingredient and digested starch.
- the starch used in the granules according to the invention is preferably obtained from comminuted cereals (eg wheat, barley, maize, rye).
- the starch forms in the granules mainly the matrix for the at least one agrochemical active ingredient to be used and prevents drug mixtures.
- the granules are designed so that it has a mass structure characterized by the particle sizes X] 0 and X 90 , where Xi 0 is generally greater than or equal to 100 ⁇ m, preferably greater than or equal to 200 ⁇ m preferably greater than or equal to 300 ⁇ m, in particular greater than or equal to 350 ⁇ m, more preferably greater than or equal to 400 ⁇ m.
- the size value x ] 0 specified for the granulate according to the invention indicates the size value which is undershot by at most 10% by mass of the particles.
- the mass structure of the granules has a size of x 9 o of generally less than 5 mm, preferably less than or equal to 2 mm, particularly preferably less than or equal to 1.75 mm, in particular less than or equal to 1.2 mm, on, wherein the value X 90 indicates the size value which is exceeded by at most 10% of the mass of the granules.
- the granule density of the granules according to the invention is generally less than 1.5 kg / dm 3 , preferably less than 1.4 kg / dm 3 , more preferably less than 1.3 kg / dm 3 , in particular less than 1.0 kg / dm 3 .
- agrochemical active substance used in the granules according to the invention is in principle subject to no restriction and all known agrochemical active substances can be used in the granules within the scope of the present invention. Examples for this are:
- Azoxystrobin Cyazofamide, Dimoxystrobin, Enestrobin, Famoxadone, Fenamidon, Fluoxastrobin, Kresoximmethyl, Metominostrobin, Orysastrobin, Pyraclostrobin, Picoxystrobin, Trifloxystrobin
- Carbamates for example alanycarb, aldicarb, aldoxycarb, allyxycarb, aminocarb, bendiocarb, benfuracarb, bufencarb, butacarb, butocarboxime, butoxycarboxime, carbaryl, carbofuran, carbosulfan, cloethocarb, dimetilane, ethiofencarb, fenobucarb, fenothiocarb, formetanate, furathiocarb, isoprocarb, metamethyl sodium, methiocarb, methomyl, metolcarb, oxamyl, pirimicarb, promecarb, propoxur, thiodicarb, thiofanox, trimethacarb, XMC, xylylcarb, triazamates
- Organophosphates for example acephates, azamethiphos, azinphos (-methyl, -ethyl), bromophos-ethyl, bromfenvinfos (-methyl), butathiofos, cadusafos, carbophenothione, chloroethoxyfos, chlorfenvinphos, chloroformes, chlorpyrifos (-methyl / -ethyl), coumaphos, Cyanofenphos, cyanophos, chlorfenvinphos, demeton-S-methyl, demeton-S-methylsulphon, dialifos, diazinon, dichlofenthione, dichlorvos / DDVP, dicrotophos, dimethoates, dimethylvinphos, dioxabenzofos, disulphoton, EPN, ethion, ethoprophos, etrimfos, famphur, fenamiphos, Fe
- Pyrethroids for example, acrinathrin, allethrin (d-cis-trans, d-trans), beta-cyfluthrin, bifenthrin, bioallethrin, bioallethrin S-cyclopentyl isomer, bioethanomethrin, biopermethrin, bioresmethrin, Chlovaporthrin, cis-cypermethrin, cis-resmethrin, cis-permethrin, clocythrin, cycloprothrin, cyfluthrin, cyhalothrin, cypermethrin (alpha-, beta-, theta-, zeta-), cyphenothrin, deltamethrin, empenthrin (IR-isomer), esfenvalerate, Etofenprox, fenfluthrin, fenpropathrin,
- Oxadiazines for example Indoxacarb
- Chloronicotinyls for example acetamipride, clothianidin, dinotefuran, imidacloprid, nitenpyram, nithiazines, thiacloprid, thiamethoxam
- Acetylcholine receptor modulators are Acetylcholine receptor modulators
- Organochlorines for example, camphechlor, chlordane, endosulfan, gamma-HCH, HCH, heptachlor, lindane, methoxychlor
- Fiproles for example, acetoprole, ethiprole, fipronil, pyrafluprole, pyriprole, vaniliprole
- Chloride channel activators Mectins for example Abamectin, Emamectin, Emamectin benzoate, Ivermectin, Lepimectin, Milbemycin
- Juvenile hormone mimetics for example, diofenolan, epofenonans, fenoxycarb, hydroprene, kinoprenes, methoprenes, pyrigiphenes, triprene
- Diacylhydrazines for example chromafenozide, Halofenozide, Methoxyfenozide, Tebufenozide
- Benzoylureas for example bistrifluron, chlorofluazuron, diflubenzuron, fluazuron, flucycloxuron, fenphenoxuron, hexaflumuron, lufenuron, novaluron, noviflumuron, penfluron, teflubenzuron, triflumuron
- Organotin compounds for example azocyclotin, cyhexatin, fenbutatin oxides
- Dinitrophenols for example binapacyrl, dinobutone, dinocap, DNOC, meptyldinocap
- METI's for example Fenazaquin, Fenpyroximate, Pyrimidifen, Pyridaben, Tebufenpyrad, Tolfenpyrad hydramethylnon
- spirodiclofen for example spirodiclofen, spiromesifen,
- rynaxypyr (3-bromo-N- ⁇ 4-chloro-2-methyl-6 - [(methylamino) carbonyl] phenyl ⁇ -1- (3-chloropyridin-2-yl) -1H-pyrazole-5-carboxamide)
- Fumigants for example aluminum phosphides, methyl bromides, sulfuryl fluorides
- Food inhibitors for example Cryolite, Flonicamid, Pymetrozine
- Mite growth inhibitors for example clofentezine, etoxazole, hexythiazox
- Gossyplure Hydramethylnone, Japonilure, Metoxadiazone, Petroleum, Piperonyl butoxide, Potassium oleate, Pyralidyl, Sulfluramide, Tetradifon, Tetrasul, Triarathene, Verbutin.
- Esters e.g. fluazifop-butyl and fluazifop-p-butyl; flucarbazone (sodium), fluchloralin; flumetsulam; flumeturon; flumiclorac (pentyl), flumioxazine (S-482); flumipropyn; fluometuron, fluorochloridone, fluorodifen; fluoroglycofen (-ethyl); flupoxam (KNW-739); flupropacil (UBIC
- flupyrsulfuron (-methyl or -sodium), flurenol (-butyl), fluridone; flurochloridone; fluroxypyr (-meptyl); flu ⁇ rimidol, flurtamone; fluthiacet (methyl), fluthiamide, fomesafen; foramsulfuron, fosamine; furyloxyfen; glufosinate (-ammonium); glyphosate (- isopropylammonium); halo safen; halosulfuron (-methyl) and its esters (e.g., methyl ester, NC-
- DPX-66037 trimeturon; tritosulfuron, tsitodef; vernolate; WL 1 10547, ie 5-phenoxy- 1- [3- (trifluoromethyl) phenyl] -1H-tetrazole; UBH-509; D-489; LS 82-556; KPP-300; NC-324; NC-330; KH-218; DPX-N8189; SC-0774; Dowco-535; DK-8910; V-53482; PP-600; MBH-001; KIH-9201; ET-751; KIH-6127, K1H-485, KIH-2023 and SYN-523.
- the agrochemically active compounds are designated either with their "common name" according to the International Organization for Standardization (ISO) or with their chemical name, possibly together with a customary code number.
- the concentration of the agrochemically active substance in the granules according to the invention is generally at least 0.001% by mass, preferably at least 0.005% by mass, more preferably at least 0.01% by mass, in particular at least 0.05% by mass, based on the granules according to the invention.
- the maximum concentration of agrochemical active ingredients in the inventive is generally at least 0.001% by mass, preferably at least 0.005% by mass, more preferably at least 0.01% by mass, in particular at least 0.05% by mass, based on the granules according to the invention.
- Granules generally at most 10% by mass, preferably at most 9% by mass, more preferably at most 8% by mass, in particular at most 7% by mass, in each case based on the granules.
- the active ingredient concentration can be controlled by an active ingredient or by a
- the granules according to the invention can basically take any form and are not subject to any restrictions in this respect. Thus, both irregular shapes and regular shape of the granules of the invention are conceivable.
- the granules can be present both as broken granules and as cut granules.
- regular shapes for example, a lens shape, a cylinder shape, a spherical shape, or a disc shape are exemplified.
- the granules may have further additives.
- additives are adhesive additives, penetration enhancers, fillers (extenders), lubricants, for example, fats or oils, dyes, fragrances, release agents and preservatives.
- adhesive additives are to be present in the granules according to the invention, these are preferably selected from the group consisting of polyvinyl alcohols, polyvinyl acetates, carboxymethyl celluloses, natural and synthetic powdery, granular or latex-form polymers, polyvinylpyrrolidines, vinylpyrrolidone-styrene copolymers, vinylpyrrolidone-vinyl acetate copolymers, Polyethylene glycol or inorganic adhesives
- the adhesive additives are present in the mixture in concentrations of generally 0 to 15% by weight, preferably 0 to 10% by weight.
- Penetrant conveyors suitable according to the invention are defined by the fact that they promote the absorption of active substance from the dry or hydrated spray coating into the cuticle. If penetration promoters are used in the granules according to the invention, these may be selected, for example, from alkanol alkoxylates of the formula (I)
- R is straight-chain or branched alkyl having 4 to 20 carbon atoms
- R ' is H, methyl, ethyl, n-propyl, i-propyl, n-butyl, i-butyl, t-butyl, n-pentyl or n-hexyl,
- AO stands for an ethylene oxide radical, a propylene oxide radical, a butylene oxide radical or for mixtures of ethylene oxide and propylene oxide radicals or for mixtures of ethylene oxide and butylene oxide radicals and
- n stands for numbers from 2 to 30.
- alkanol alkoxylates are generally defined by the above formulas. These substances are mixtures of substances of the specified type with different chain lengths. For the indices, therefore, average values are calculated, which can also differ from whole numbers.
- fatty alcohol ethoxylates of the general formula (I-1) are particularly suitable.
- n stands for average values between 8.0 and 13.0, preferably 9.0 and 12.0, particularly preferably 10.5, and
- o for average values between 6.0 and 17.0, preferably 7.0 and 9.0, particularly preferably 8.4.
- Suitable penetration promoters are further customary surface-active substances used in formulations of agrochemical active substances. May be mentioned by way of example ethoxylated nonylphenols, tributylphenol polyglycol ethers, reaction products of alkylphenols with ethylene oxide and / or propylene oxide, alkoxylated alkylamines, alkoxylated mono-, di- or triglycerides, polyethylene oxide-sorbitan fatty acid esters, fatty acid polyglycol ether esters, diesters and diethers of polyalkylene oxides, fatty acid ester ethoxylates and alkylethoxylates and alkylarylethoxylates which are phosphated and optionally be neutralized with bases.
- anionic surfactants are all substances of this type which can usually be used in agrochemical compositions. Preference is given to alkali metal, ammonium and alkaline earth metal salts of alkylsulfonic acids or alkylarylsulfonic acids, and also alkyl (poly) ethylene glycol ether sulfates or sulfonates.
- Non-surface-active penetration promoters include fatty acid esters, mono- and diesters of dicarboxylic acids and phosphate esters.
- fragrances natural and synthetic fragrances can be used.
- fragrances may be selected, for example, from the group consisting of musk, civet, amber, castereum and similar fragrances: ajowa oil, almond oil, ambrette seed absol., Angelica root oil, anisole, basil oil, bay oil, benzoin resinoid, bergamot essence, birch oil, rosewood oil, pfriemengraut absol.
- Cajeput oil cananga oil, gapiscum oil, caraway oil, cardamon oil, carrot seed oil, cassia oil, cedarwood oil, celery seed oil, cinnamon bark oil, citronella oil, clary sage oil, clove oil, cognac oil, coriander oil, cube oil, camphor oil, dill oil, tarragon oil.
- Eucalyptus oil sweet fennel oil, calbanum resinoid, garlic oil, geranium oil, ginger oil, grapefruit oil, hop oil, hyacinth absolute, jasmine absol.
- Juniper berry oil labdanum resinoid, lavender oil, bay leaf oil, lemon oil, lemonsgrass oil, lovage oil, mace oil, tangerine oil, Nfisoma absol., Myrrh absol.
- Pinene, limonene and similar hydrocarbons 3,3,5-trimethylcyclohexanol, linalool, geraniol, nerol, citronellol, menthol, borneol, bomeylmethoxycyclohexanol, benzyl alcohol, anisalcohol, cinnamyl alcohol, ⁇ -phenylethyl alcohol, cis-3-hexanol, te ⁇ ineol and similar alcohols; Anetholes, musk xylene, isoeugenol, methyleugenol and like phenols; Amylcinnamaldehyde, anisaldehyde, n-butyraldehyde, cuminaldehyde, cyclamenaldehyde, decylaldehyde, isobutyraldehyde, hexylaldehyde, heptylaldehyde, n
- fragrances may be used alone, or at least two of them may be used in admixture with each other.
- the formulation according to the invention may optionally additionally contain the additives customary in the fragrance industry, such as patchouli oil or similar volatility-inhibiting agents, such as eugenol or similar viscosity-regulating agents.
- the products of the invention may also contain deodorants, e.g. Lauryl methacrylate, geranyl crotonate, acetophenone myristate, p-methylacetophenone-benzaldehyde, benzyl acetate, benzyl propionate, amyl cinnamaldehyde, anisaldehyde, diphenyloxide, methyl benzoate, ethyl benzoate, methyl phenylacetate, ethyl phenylacetate, neoline, safrol, etc.
- deodorants e.g. Lauryl methacrylate, geranyl crotonate, acetophenone myristate, p-methylacetophenone-benzaldehyde, benzyl acetate, benzyl propionate, amyl cinnamaldehyde, anisaldehyde, diphenyloxide, methyl benzoate
- the granules according to the invention may have a certain residual moisture. It is preferred that the residual moisture of the granules is adjusted so that it does not come to a swelling of the starch during storage of the granules. In addition, it is preferred that the residual moisture of the granules is adjusted so that the resulting granules according to the invention are storage-stable against microbial attacks, i. it e.g. does not come to a mold of the granules.
- these properties are achieved in the granules according to the invention without the use of preservatives, it being expressly pointed out that the use of a preservative in the granules according to the invention is also included in the present invention.
- the residual moisture content of the granulate according to the invention is less than 25%, preferably less than 20%, particularly preferably less than 14%.
- the storage stability of the granules, in particular at a residual moisture content of less than 14%, is achieved without the use of preservatives in the granules according to the invention.
- the granulate according to the invention is essentially such that the active ingredients and additives in the granules are largely homogeneously distributed and, in contrast to untreated pulverulent mixtures, do not separate significantly during their transport, storage and application.
- the granules according to the invention has bulk densities of generally from 50 to 1000 g / dm 3, preferably 90 to 800 g / dm 3, particularly preferably 400 to 700 g / dm 3 at.
- the present invention furthermore relates to a process for the production of a granulate which comprises at least one agrochemical active ingredient and digested starch and is largely free of dust and segregation.
- the process according to the invention is characterized in that the granules are produced by hydrothermal-mechanical processes (e.g., expanding, extruding, flocculating) with or without final structuring.
- the temperature during these processes 90 to 130 0 C.
- a short time is understood to mean a maximum period of one minute or less.
- hydrothermal-mechanical processes can be carried out in any suitable device known per se to a person skilled in the art.
- these processes can be carried out in a screw extruder or in an expander.
- the granules premix in this process become so intense after the addition of water and / or steam, if appropriate in an upstream conditioning device in the screw extruder
- an upstream conditioning device in the screw extruder
- shear and thermal stress that the strength of the cereal is digested and gelatiniert and structuring of the granules takes place.
- a subsequent drying and cooling process determines the residual moisture and curing of the granules.
- the hydrothermal-mechanical processes of the process according to the invention are carried out in an expander.
- the procedure in the production of the granules according to the invention can preferably take place as follows:
- a premix of the agrochemically active substance and a correspondingly required amount of a starchy substance is produced. If appropriate, this premix can be mixed with other auxiliaries which have been mentioned in the preparation of the granules according to the invention.
- this mixture is then subsequently mixed with saturated steam and / or water and then fed to the hydrothermal-mechanical processes in an expander.
- the hydrothermal-mechanical processes are carried out without the agrochemical active substance (s) and additives or only with proportions of these substances, i. Only the matrix-forming formulation constituents of the granules according to the invention are exposed to the hydrothermal-mechanical processes.
- the agrochemical active ingredients and additives are sprayed in this embodiment of the method according to the invention on the granules produced by the hydrothermal-mechanical processes in liquid form at ambient pressure or applied under vacuum. This procedure is always preferred if the agrochemical active substance (s) and / or the additives are not to be exposed to the hydrothermal-mechanical stress.
- the resulting granules subjected to flash evaporation can be fed either after drying and / or cooling processes or directly to comminution.
- the comminution of the granules thus obtained can take place, for example, in one or more stages.
- the granule size can also be adjusted by means of a mill, in particular a roll mill or a sieve, for example a pass sieve.
- the return of the undersize and / or oversize is provided.
- Granules obtainable by this process are preferably the granules described in more detail above.
- Another object of the present invention is a granulate, which is obtainable by a method as described above.
- the present invention relates to the use of the granules according to the invention as crop protection agents, in particular for leaf penetration and bait formulation.
- the granules according to the invention are preferably applied to the leaf surfaces at a residual moisture content.
- the application of the granules according to the invention can be carried out, for example, when the individual plants are still covered with morning dew.
- the granules of the present invention substantially adhere to the moisturized sheet surface.
- the penetrant may first permeabilize the cuticle of the leaf for the drug to allow the drug to penetrate into the leaf.
- the residence time of the granules on the sheet must be sufficiently large to ensure a complete release of the active ingredient from the granules into the plant.
- the granules of the invention are preferably formed so that the granules dissolve after a certain time and leave no residue on the leaves.
- the granules of the invention In order for the granules of the invention to accomplish this task, they must not be too heavy and too large to adhere to the leaves.
- the granules according to the invention are preferably dust-free for reasons of handling, segregation and carryover avoidance and acceptance by the user.
- the application of the granules can be done with otherwise usually used for the spreading of granules on the ground spreaders, since the granules of the invention has a good flowability as a bulk material. Furthermore, it is preferred if the agrochemical active ingredient in the granules has a homogeneous distribution, so that reliable activity is possible even with a low active ingredient concentration and thus small amounts of active ingredient.
- the following granules are prepared with the following formulations (all figures in% by weight) by means of an expander, each of these formulations being produced at two different operating conditions of the expander.
- the active substance is fenoxaprop-P-ethyl and the penetration aid used is Genapol® X 60.
- a premix of micronized drug, the penetration aid and a certain amount of wheat vapor is prepared.
- This premix is mixed in the main mixer with most of the wheat vapor and the rest of the recipe ingredients.
- water and / or saturated steam is added to this mixture.
- the hydrothermal-mechanical treatment is then carried out in an expander.
- the expandat is structured and cooled in a primary crusher.
- the granule size is adjusted by means of a roller mill and sieving.
- the biological effectiveness of the granules against the relevant weed "Crabgrass" is at least 72 to 95%.
Landscapes
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- Agronomy & Crop Science (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Toxicology (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Fertilizers (AREA)
Abstract
Description
Claims
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE102006055477A DE102006055477A1 (de) | 2006-11-24 | 2006-11-24 | Pflanzenschutzgranulate zur Applikation auf die Blattoberfläche |
| PCT/EP2007/009825 WO2008061655A2 (de) | 2006-11-24 | 2007-11-14 | Pflanzenschutzgranulate zur applikation auf die blattoberfläche |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| EP2106211A2 true EP2106211A2 (de) | 2009-10-07 |
Family
ID=38895970
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EP07846579A Withdrawn EP2106211A2 (de) | 2006-11-24 | 2007-11-14 | Pflanzenschutzgranulate zur applikation auf die blattoberfläche |
Country Status (9)
| Country | Link |
|---|---|
| US (1) | US8323697B2 (de) |
| EP (1) | EP2106211A2 (de) |
| JP (1) | JP2010510261A (de) |
| AU (1) | AU2007323417A1 (de) |
| BR (1) | BRPI0718954A2 (de) |
| CA (1) | CA2670240A1 (de) |
| DE (1) | DE102006055477A1 (de) |
| WO (1) | WO2008061655A2 (de) |
| ZA (1) | ZA200903437B (de) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA2729618C (en) * | 2008-07-03 | 2016-05-31 | Ishihara Sangyo Kaisha, Ltd. | Fungicidal composition and method for controlling plant diseases |
| DE102008037631A1 (de) | 2008-08-14 | 2010-02-18 | Bayer Cropscience Ag | Herbizid-Kombination mit Dimethoxytriazinyl-substituierten Difluormethansulfonylaniliden |
| KR20110097840A (ko) * | 2008-11-17 | 2011-08-31 | 바스프 에스이 | 전분 함유 과립 제제 |
| WO2012102703A1 (en) * | 2011-01-25 | 2012-08-02 | The Anderson, Inc . | Dispersible adhesive granules |
| CN113854311B (zh) * | 2021-10-13 | 2022-08-02 | 万华化学集团股份有限公司 | 一种增效除草组合物及其制剂与应用 |
| US12593840B2 (en) | 2022-01-24 | 2026-04-07 | Optimally Balanced Corp. | Pesticidal or repellant composition and method of use |
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| IL31939A0 (en) * | 1968-04-03 | 1969-06-25 | Diamond Shamrock Corp | Granular pesticidal compositions |
| US3843783A (en) * | 1971-11-08 | 1974-10-22 | Velsicol Chemical Corp | Rodenticidal compositions and processes employing gelatinized amylaceous materials |
| CA1040451A (en) * | 1976-04-12 | 1978-10-17 | Cyril T. Jones | Production of a coal-base soil beneficiating pellet containing active slow-release granules in a starch and hydrocarbon solid |
| CS192763B1 (en) * | 1977-04-08 | 1979-09-17 | Miroslav Cap | Method of machanic and hydrotechnical treatment of the grain products |
| JPS57109702A (en) * | 1980-12-26 | 1982-07-08 | Kumiai Chem Ind Co Ltd | Powdered agricultural chemical emulsion |
| JPS6036402A (ja) * | 1983-08-09 | 1985-02-25 | Nichiden Kagaku Kk | 農薬組成物 |
| CA1265044A (en) | 1984-03-14 | 1990-01-30 | Stan J. Flashinski | Gelatinized starch matrix insect bait |
| JPS62120301A (ja) * | 1985-11-19 | 1987-06-01 | Hokko Chem Ind Co Ltd | 改良された農薬粉剤 |
| DE3542440A1 (de) * | 1985-11-30 | 1987-06-04 | Hoechst Ag | Neue wasserdispergierbare granulate |
| US4859377A (en) * | 1987-07-10 | 1989-08-22 | The United States Of America, As Represented By The Secretary Of Agriculture | Starch encapsulation of entomopathogens |
| DE3739088A1 (de) * | 1987-11-18 | 1989-06-01 | Zucker Friedrich J | Verfahren zur herstellung von stabilisierten duengemitteln |
| US4985082A (en) | 1987-11-20 | 1991-01-15 | Lafayette Applied Chemistry, Inc. | Microporous granular starch matrix compositions |
| JPH0714841B2 (ja) * | 1987-12-15 | 1995-02-22 | 第一工業製薬株式会社 | 農薬水和剤用分散剤組成物 |
| US4963179A (en) * | 1988-09-14 | 1990-10-16 | Givaudan Corporation | Preservatives containing β-bromo-β-nitrostyrene for use in aqueous systems |
| IL94588A0 (en) * | 1989-06-22 | 1991-04-15 | Warner Lambert Co | Polymer base blend compositions containing destructurized starch |
| YU129090A (sh) | 1989-07-11 | 1992-12-21 | Warner-Lambert Company | Preparati polimernih smeša koji sadrže destrukturisani skrob |
| DE4127757A1 (de) * | 1991-02-06 | 1992-08-13 | Hoechst Ag | Neue pflanzenschutzmittel-formulierungen |
| AU1589492A (en) * | 1991-03-01 | 1992-10-06 | Warner-Lambert Company | Starch-based controlled release compositions |
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2006
- 2006-11-24 DE DE102006055477A patent/DE102006055477A1/de not_active Withdrawn
-
2007
- 2007-11-14 BR BRPI0718954-0A patent/BRPI0718954A2/pt not_active IP Right Cessation
- 2007-11-14 EP EP07846579A patent/EP2106211A2/de not_active Withdrawn
- 2007-11-14 US US12/515,486 patent/US8323697B2/en active Active
- 2007-11-14 AU AU2007323417A patent/AU2007323417A1/en not_active Abandoned
- 2007-11-14 WO PCT/EP2007/009825 patent/WO2008061655A2/de not_active Ceased
- 2007-11-14 JP JP2009537513A patent/JP2010510261A/ja active Pending
- 2007-11-14 CA CA002670240A patent/CA2670240A1/en not_active Abandoned
-
2009
- 2009-05-19 ZA ZA200903437A patent/ZA200903437B/xx unknown
Non-Patent Citations (1)
| Title |
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| See references of WO2008061655A2 * |
Also Published As
| Publication number | Publication date |
|---|---|
| WO2008061655A3 (de) | 2009-04-23 |
| CA2670240A1 (en) | 2008-05-29 |
| ZA200903437B (en) | 2010-07-28 |
| WO2008061655A2 (de) | 2008-05-29 |
| BRPI0718954A2 (pt) | 2013-12-17 |
| US8323697B2 (en) | 2012-12-04 |
| JP2010510261A (ja) | 2010-04-02 |
| AU2007323417A1 (en) | 2008-05-29 |
| US20090274767A1 (en) | 2009-11-05 |
| DE102006055477A1 (de) | 2008-05-29 |
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