HUT71707A - Method for lightening of cleanout spray tank - Google Patents

Method for lightening of cleanout spray tank Download PDF

Info

Publication number: HUT71707A
Authority: HU; Hungary
Prior art keywords: methyl; amino; carbonyl; alkyl; sulfonylurea
Prior art date: 1992-02-19

Application number

HU9402407A

Other languages

English (en)

Hungarian (hu)

Other versions

HU9402407D0 (en

Inventor

Luann Marshall Pugh

William Robert Cahill

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.)

1992-02-19

Filing date

1993-02-12

Publication date

1996-01-29

1993-02-12 Application filed by Du Pont filed Critical Du Pont

1994-11-28 Publication of HU9402407D0 publication Critical patent/HU9402407D0/hu

1996-01-29 Publication of HUT71707A publication Critical patent/HUT71707A/hu

Links

239000007921 spray Substances 0.000 title claims description 34
238000000034 method Methods 0.000 title claims description 23
YROXIXLRRCOBKF-UHFFFAOYSA-N sulfonylurea Chemical class OC(=N)N=S(=O)=O YROXIXLRRCOBKF-UHFFFAOYSA-N 0.000 claims description 58
229940100389 Sulfonylurea Drugs 0.000 claims description 52
125000000217 alkyl group Chemical group 0.000 claims description 31
239000000203 mixture Substances 0.000 claims description 30
229910052739 hydrogen Inorganic materials 0.000 claims description 27
239000001257 hydrogen Substances 0.000 claims description 24
125000003545 alkoxy group Chemical group 0.000 claims description 21
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 21
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 18
125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 15
125000001309 chloro group Chemical group Cl* 0.000 claims description 14
AHTPATJNIAFOLR-UHFFFAOYSA-N thifensulfuron-methyl Chemical group S1C=CC(S(=O)(=O)NC(=O)NC=2N=C(OC)N=C(C)N=2)=C1C(=O)OC AHTPATJNIAFOLR-UHFFFAOYSA-N 0.000 claims description 13
-1 1- C 4 -C 4 alkoxy Chemical group 0.000 claims description 12
239000005623 Thifensulfuron-methyl Substances 0.000 claims description 12
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 claims description 12
150000003839 salts Chemical class 0.000 claims description 12
125000001246 bromo group Chemical group Br* 0.000 claims description 11
125000001153 fluoro group Chemical group F* 0.000 claims description 11
238000009472 formulation Methods 0.000 claims description 11
125000004765 (C1-C4) haloalkyl group Chemical group 0.000 claims description 8
125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims description 8
125000000262 haloalkenyl group Chemical group 0.000 claims description 8
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 8
DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical group 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 claims description 7
229910052801 chlorine Inorganic materials 0.000 claims description 7
229910052731 fluorine Inorganic materials 0.000 claims description 7
239000011734 sodium Substances 0.000 claims description 7
229910052708 sodium Inorganic materials 0.000 claims description 7
125000004767 (C1-C4) haloalkoxy group Chemical group 0.000 claims description 6
125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 claims description 6
ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical group [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 claims description 6
239000000460 chlorine Substances 0.000 claims description 6
239000011737 fluorine Substances 0.000 claims description 6
239000011591 potassium Chemical group 0.000 claims description 6
229910052700 potassium Inorganic materials 0.000 claims description 6
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 5
PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims description 5
125000005083 alkoxyalkoxy group Chemical group 0.000 claims description 5
229910052794 bromium Inorganic materials 0.000 claims description 5
229910052736 halogen Inorganic materials 0.000 claims description 5
150000002367 halogens Chemical group 0.000 claims description 5
RSMUVYRMZCOLBH-UHFFFAOYSA-N metsulfuron methyl Chemical compound COC(=O)C1=CC=CC=C1S(=O)(=O)NC(=O)NC1=NC(C)=NC(OC)=N1 RSMUVYRMZCOLBH-UHFFFAOYSA-N 0.000 claims description 5
239000000575 pesticide Substances 0.000 claims description 5
YMXOXAPKZDWXLY-QWRGUYRKSA-N tribenuron methyl Chemical group COC(=O)[C@H]1CCCC[C@@H]1S(=O)(=O)NC(=O)N(C)C1=NC(C)=NC(OC)=N1 YMXOXAPKZDWXLY-QWRGUYRKSA-N 0.000 claims description 5
125000006559 (C1-C3) alkylamino group Chemical group 0.000 claims description 4
125000001494 2-propynyl group Chemical group [H]C#CC([H])([H])* 0.000 claims description 4
OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical group [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 claims description 4
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 4
125000004183 alkoxy alkyl group Chemical group 0.000 claims description 4
125000003282 alkyl amino group Chemical group 0.000 claims description 4
125000004414 alkyl thio group Chemical group 0.000 claims description 4
239000011575 calcium Chemical group 0.000 claims description 4
229910052791 calcium Inorganic materials 0.000 claims description 4
125000004432 carbon atom Chemical group C* 0.000 claims description 4
NSWAMPCUPHPTTC-UHFFFAOYSA-N chlorimuron-ethyl Chemical compound CCOC(=O)C1=CC=CC=C1S(=O)(=O)NC(=O)NC1=NC(Cl)=CC(OC)=N1 NSWAMPCUPHPTTC-UHFFFAOYSA-N 0.000 claims description 4
238000011109 contamination Methods 0.000 claims description 4
125000004093 cyano group Chemical group *C#N 0.000 claims description 4
125000004995 haloalkylthio group Chemical group 0.000 claims description 4
RTCOGUMHFFWOJV-UHFFFAOYSA-N nicosulfuron Chemical compound COC1=CC(OC)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CN=2)C(=O)N(C)C)=N1 RTCOGUMHFFWOJV-UHFFFAOYSA-N 0.000 claims description 4
MEFOUWRMVYJCQC-UHFFFAOYSA-N rimsulfuron Chemical compound CCS(=O)(=O)C1=CC=CN=C1S(=O)(=O)NC(=O)NC1=NC(OC)=CC(OC)=N1 MEFOUWRMVYJCQC-UHFFFAOYSA-N 0.000 claims description 4
ZDXMLEQEMNLCQG-UHFFFAOYSA-N sulfometuron methyl Chemical compound COC(=O)C1=CC=CC=C1S(=O)(=O)NC(=O)NC1=NC(C)=CC(C)=N1 ZDXMLEQEMNLCQG-UHFFFAOYSA-N 0.000 claims description 4
125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 claims description 4
QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical group [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims description 3
125000005210 alkyl ammonium group Chemical group 0.000 claims description 3
125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 3
125000006273 (C1-C3) alkyl group Chemical group 0.000 claims description 2
125000006583 (C1-C3) haloalkyl group Chemical group 0.000 claims description 2
125000006650 (C2-C4) alkynyl group Chemical group 0.000 claims description 2
125000004793 2,2,2-trifluoroethoxy group Chemical group FC(CO*)(F)F 0.000 claims description 2
125000006012 2-chloroethoxy group Chemical group 0.000 claims description 2
KHBQMWCZKVMBLN-UHFFFAOYSA-N Benzenesulfonamide Chemical compound NS(=O)(=O)C1=CC=CC=C1 KHBQMWCZKVMBLN-UHFFFAOYSA-N 0.000 claims description 2
239000005586 Nicosulfuron Substances 0.000 claims description 2
BGNQYGRXEXDAIQ-UHFFFAOYSA-N Pyrazosulfuron-ethyl Chemical compound C1=NN(C)C(S(=O)(=O)NC(=O)NC=2N=C(OC)C=C(OC)N=2)=C1C(=O)OCC BGNQYGRXEXDAIQ-UHFFFAOYSA-N 0.000 claims description 2
239000005616 Rimsulfuron Substances 0.000 claims description 2
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 2
125000003302 alkenyloxy group Chemical group 0.000 claims description 2
125000005133 alkynyloxy group Chemical group 0.000 claims description 2
125000004397 aminosulfonyl group Chemical group NS(=O)(=O)* 0.000 claims description 2
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 2
125000000852 azido group Chemical group *N=[N+]=[N-] 0.000 claims 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 claims description 2
XMQFTWRPUQYINF-UHFFFAOYSA-N bensulfuron-methyl Chemical compound COC(=O)C1=CC=CC=C1CS(=O)(=O)NC(=O)NC1=NC(OC)=CC(OC)=N1 XMQFTWRPUQYINF-UHFFFAOYSA-N 0.000 claims description 2
229910052799 carbon Inorganic materials 0.000 claims description 2
150000001768 cations Chemical class 0.000 claims description 2
125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims description 2
ZINJLDJMHCUBIP-UHFFFAOYSA-N ethametsulfuron-methyl Chemical compound CCOC1=NC(NC)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2)C(=O)OC)=N1 ZINJLDJMHCUBIP-UHFFFAOYSA-N 0.000 claims description 2
125000004438 haloalkoxy group Chemical group 0.000 claims description 2
125000001188 haloalkyl group Chemical group 0.000 claims description 2
125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 2
DTVOKYWXACGVGO-UHFFFAOYSA-N methyl 2-[(4,6-dimethoxypyrimidin-2-yl)carbamoylsulfamoyl]-6-(trifluoromethyl)pyridine-3-carboxylate Chemical compound COC(=O)C1=CC=C(C(F)(F)F)N=C1S(=O)(=O)NC(=O)NC1=NC(OC)=CC(OC)=N1 DTVOKYWXACGVGO-UHFFFAOYSA-N 0.000 claims description 2
UUEVFMOUBSLVJW-UHFFFAOYSA-N oxo-[[1-[2-[2-[2-[4-(oxoazaniumylmethylidene)pyridin-1-yl]ethoxy]ethoxy]ethyl]pyridin-4-ylidene]methyl]azanium;dibromide Chemical group [Br-].[Br-].C1=CC(=C[NH+]=O)C=CN1CCOCCOCCN1C=CC(=C[NH+]=O)C=C1 UUEVFMOUBSLVJW-UHFFFAOYSA-N 0.000 claims description 2
229910052760 oxygen Inorganic materials 0.000 claims description 2
239000001301 oxygen Substances 0.000 claims description 2
125000004076 pyridyl group Chemical group 0.000 claims description 2
SNOOUWRIMMFWNE-UHFFFAOYSA-M sodium;6-[(3,4,5-trimethoxybenzoyl)amino]hexanoate Chemical compound [Na+].COC1=CC(C(=O)NCCCCCC([O-])=O)=CC(OC)=C1OC SNOOUWRIMMFWNE-UHFFFAOYSA-M 0.000 claims description 2
125000005346 substituted cycloalkyl group Chemical group 0.000 claims description 2
229910052717 sulfur Chemical group 0.000 claims description 2
239000011593 sulfur Chemical group 0.000 claims description 2
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims 4
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims 4
125000006645 (C3-C4) cycloalkyl group Chemical group 0.000 claims 1
XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims 1
WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 claims 1
230000015572 biosynthetic process Effects 0.000 claims 1
239000004202 carbamide Substances 0.000 claims 1
125000005843 halogen group Chemical group 0.000 claims 1
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 27
239000005822 Propiconazole Substances 0.000 description 22
STJLVHWMYQXCPB-UHFFFAOYSA-N propiconazole Chemical compound O1C(CCC)COC1(C=1C(=CC(Cl)=CC=1)Cl)CN1N=CN=C1 STJLVHWMYQXCPB-UHFFFAOYSA-N 0.000 description 22
QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 14
239000000243 solution Substances 0.000 description 14
239000005631 2,4-Dichlorophenoxyacetic acid Substances 0.000 description 13
238000004140 cleaning Methods 0.000 description 13
239000005574 MCPA Substances 0.000 description 10
WHKUVVPPKQRRBV-UHFFFAOYSA-N Trasan Chemical compound CC1=CC(Cl)=CC=C1OCC(O)=O WHKUVVPPKQRRBV-UHFFFAOYSA-N 0.000 description 10
VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 7
241000196324 Embryophyta Species 0.000 description 7
229910021529 ammonia Inorganic materials 0.000 description 7
239000000908 ammonium hydroxide Substances 0.000 description 7
150000001875 compounds Chemical class 0.000 description 7
239000000725 suspension Substances 0.000 description 7
239000002253 acid Substances 0.000 description 6
239000003085 diluting agent Substances 0.000 description 6
239000008187 granular material Substances 0.000 description 6
239000004094 surface-active agent Substances 0.000 description 6
238000012360 testing method Methods 0.000 description 6
239000002245 particle Substances 0.000 description 5
239000008188 pellet Substances 0.000 description 5
239000000843 powder Substances 0.000 description 5
238000005507 spraying Methods 0.000 description 5
JWUCHKBSVLQQCO-UHFFFAOYSA-N 1-(2-fluorophenyl)-1-(4-fluorophenyl)-2-(1H-1,2,4-triazol-1-yl)ethanol Chemical compound C=1C=C(F)C=CC=1C(C=1C(=CC=CC=1)F)(O)CN1C=NC=N1 JWUCHKBSVLQQCO-UHFFFAOYSA-N 0.000 description 4
241000335053 Beta vulgaris Species 0.000 description 4
239000005787 Flutriafol Substances 0.000 description 4
238000004166 bioassay Methods 0.000 description 4
239000007788 liquid Substances 0.000 description 4
XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 description 4
235000016068 Berberis vulgaris Nutrition 0.000 description 3
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
239000004480 active ingredient Substances 0.000 description 3
239000012141 concentrate Substances 0.000 description 3
239000012530 fluid Substances 0.000 description 3
239000013505 freshwater Substances 0.000 description 3
238000002156 mixing Methods 0.000 description 3
239000013049 sediment Substances 0.000 description 3
239000002904 solvent Substances 0.000 description 3
239000000126 substance Substances 0.000 description 3
239000004562 water dispersible granule Substances 0.000 description 3
241000219310 Beta vulgaris subsp. vulgaris Species 0.000 description 2
FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 2
239000005584 Metsulfuron-methyl Substances 0.000 description 2
235000021536 Sugar beet Nutrition 0.000 description 2
238000005054 agglomeration Methods 0.000 description 2
230000002776 aggregation Effects 0.000 description 2
150000003863 ammonium salts Chemical class 0.000 description 2
238000004458 analytical method Methods 0.000 description 2
230000008901 benefit Effects 0.000 description 2
239000000969 carrier Substances 0.000 description 2
239000003795 chemical substances by application Substances 0.000 description 2
239000003599 detergent Substances 0.000 description 2
239000004495 emulsifiable concentrate Substances 0.000 description 2
239000000839 emulsion Substances 0.000 description 2
230000007613 environmental effect Effects 0.000 description 2
238000011049 filling Methods 0.000 description 2
239000000499 gel Substances 0.000 description 2
239000002917 insecticide Substances 0.000 description 2
239000011777 magnesium Substances 0.000 description 2
229910052749 magnesium Inorganic materials 0.000 description 2
239000000463 material Substances 0.000 description 2
PSZYNBSKGUBXEH-UHFFFAOYSA-M naphthalene-1-sulfonate Chemical compound C1=CC=C2C(S(=O)(=O)[O-])=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-M 0.000 description 2
238000002360 preparation method Methods 0.000 description 2
239000003826 tablet Substances 0.000 description 2
229910002012 Aerosil® Inorganic materials 0.000 description 1
239000002028 Biomass Substances 0.000 description 1
KZBUYRJDOAKODT-UHFFFAOYSA-N Chlorine Chemical group ClCl KZBUYRJDOAKODT-UHFFFAOYSA-N 0.000 description 1
239000005496 Chlorsulfuron Substances 0.000 description 1
YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 1
BIVQBWSIGJFXLF-UHFFFAOYSA-N PPM-18 Chemical compound C=1C(=O)C2=CC=CC=C2C(=O)C=1NC(=O)C1=CC=CC=C1 BIVQBWSIGJFXLF-UHFFFAOYSA-N 0.000 description 1
PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 1
239000005708 Sodium hypochlorite Substances 0.000 description 1
101100054666 Streptomyces halstedii sch3 gene Proteins 0.000 description 1
WSNSMPZJJIYZCV-UHFFFAOYSA-N [Na]C Chemical class [Na]C WSNSMPZJJIYZCV-UHFFFAOYSA-N 0.000 description 1
230000002378 acidificating effect Effects 0.000 description 1
239000000654 additive Substances 0.000 description 1
229910052783 alkali metal Inorganic materials 0.000 description 1
239000002518 antifoaming agent Substances 0.000 description 1
239000004599 antimicrobial Substances 0.000 description 1
238000003556 assay Methods 0.000 description 1
229960000892 attapulgite Drugs 0.000 description 1
239000000440 bentonite Substances 0.000 description 1
229910000278 bentonite Inorganic materials 0.000 description 1
SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 1
239000000872 buffer Substances 0.000 description 1
239000007853 buffer solution Substances 0.000 description 1
RYAGRZNBULDMBW-UHFFFAOYSA-L calcium;3-(2-hydroxy-3-methoxyphenyl)-2-[2-methoxy-4-(3-sulfonatopropyl)phenoxy]propane-1-sulfonate Chemical compound [Ca+2].COC1=CC=CC(CC(CS([O-])(=O)=O)OC=2C(=CC(CCCS([O-])(=O)=O)=CC=2)OC)=C1O RYAGRZNBULDMBW-UHFFFAOYSA-L 0.000 description 1
239000003518 caustics Substances 0.000 description 1
238000003889 chemical engineering Methods 0.000 description 1
230000000052 comparative effect Effects 0.000 description 1
125000000753 cycloalkyl group Chemical group 0.000 description 1
230000034994 death Effects 0.000 description 1
230000008021 deposition Effects 0.000 description 1
GUJOJGAPFQRJSV-UHFFFAOYSA-N dialuminum;dioxosilane;oxygen(2-);hydrate Chemical compound O.[O-2].[O-2].[O-2].[Al+3].[Al+3].O=[Si]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O GUJOJGAPFQRJSV-UHFFFAOYSA-N 0.000 description 1
JYIMWRSJCRRYNK-UHFFFAOYSA-N dialuminum;disodium;oxygen(2-);silicon(4+);hydrate Chemical compound O.[O-2].[O-2].[O-2].[O-2].[O-2].[O-2].[Na+].[Na+].[Al+3].[Al+3].[Si+4] JYIMWRSJCRRYNK-UHFFFAOYSA-N 0.000 description 1
YDEXUEFDPVHGHE-GGMCWBHBSA-L disodium;(2r)-3-(2-hydroxy-3-methoxyphenyl)-2-[2-methoxy-4-(3-sulfonatopropyl)phenoxy]propane-1-sulfonate Chemical compound [Na+].[Na+].COC1=CC=CC(C[C@H](CS([O-])(=O)=O)OC=2C(=CC(CCCS([O-])(=O)=O)=CC=2)OC)=C1O YDEXUEFDPVHGHE-GGMCWBHBSA-L 0.000 description 1
238000004090 dissolution Methods 0.000 description 1
239000000428 dust Substances 0.000 description 1
239000003995 emulsifying agent Substances 0.000 description 1
238000011156 evaluation Methods 0.000 description 1
238000005243 fluidization Methods 0.000 description 1
238000011010 flushing procedure Methods 0.000 description 1
239000000417 fungicide Substances 0.000 description 1
238000000227 grinding Methods 0.000 description 1
239000004009 herbicide Substances 0.000 description 1
208000006278 hypochromic anemia Diseases 0.000 description 1
238000002347 injection Methods 0.000 description 1
239000007924 injection Substances 0.000 description 1
239000000543 intermediate Substances 0.000 description 1
239000007937 lozenge Substances 0.000 description 1
229910052901 montmorillonite Inorganic materials 0.000 description 1
230000017074 necrotic cell death Effects 0.000 description 1
239000003960 organic solvent Substances 0.000 description 1
229910052625 palygorskite Inorganic materials 0.000 description 1
235000020030 perry Nutrition 0.000 description 1
239000003090 pesticide formulation Substances 0.000 description 1
239000000546 pharmaceutical excipient Substances 0.000 description 1
230000000704 physical effect Effects 0.000 description 1
159000000001 potassium salts Chemical class 0.000 description 1
238000000746 purification Methods 0.000 description 1
239000011833 salt mixture Substances 0.000 description 1
239000000377 silicon dioxide Substances 0.000 description 1
SUKJFIGYRHOWBL-UHFFFAOYSA-N sodium hypochlorite Chemical compound [Na+].Cl[O-] SUKJFIGYRHOWBL-UHFFFAOYSA-N 0.000 description 1
239000002689 soil Substances 0.000 description 1
239000007787 solid Substances 0.000 description 1
239000008247 solid mixture Substances 0.000 description 1
238000003756 stirring Methods 0.000 description 1
208000024891 symptom Diseases 0.000 description 1
150000003672 ureas Chemical class 0.000 description 1
238000001238 wet grinding Methods 0.000 description 1
239000004563 wettable powder Substances 0.000 description 1
239000002023 wood Substances 0.000 description 1

Classifications

- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
- A01N47/28—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N<
- A01N47/36—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N< containing the group >N—CO—N< directly attached to at least one heterocyclic ring; Thio analogues thereof

Landscapes

Life Sciences & Earth Sciences (AREA)
Agronomy & Crop Science (AREA)
Pest Control & Pesticides (AREA)
Plant Pathology (AREA)
Health & Medical Sciences (AREA)
Engineering & Computer Science (AREA)
Dentistry (AREA)
General Health & Medical Sciences (AREA)
Wood Science & Technology (AREA)
Zoology (AREA)
Environmental Sciences (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Application Of Or Painting With Fluid Materials (AREA)

HU9402407A 1992-02-19 1993-02-12 Method for lightening of cleanout spray tank HUT71707A (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US83859092A	1992-02-19	1992-02-19

Publications (2)

Publication Number	Publication Date
HU9402407D0 HU9402407D0 (en)	1994-11-28
HUT71707A true HUT71707A (en)	1996-01-29

Family

ID=25277514

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
HU9402407A HUT71707A (en)	1992-02-19	1993-02-12	Method for lightening of cleanout spray tank

Country Status (11)

Country	Link
EP (1)	EP0626807A1 (lt)
JP (1)	JPH07503973A (lt)
CN (1)	CN1077838A (lt)
AU (1)	AU3618793A (lt)
BR (1)	BR9305997A (lt)
CA (1)	CA2130118A1 (lt)
HU (1)	HUT71707A (lt)
LT (1)	LT3009B (lt)
RU (1)	RU94040706A (lt)
WO (1)	WO1993016596A1 (lt)
ZA (1)	ZA931139B (lt)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
AR041211A1 (es) *	2002-09-12	2005-05-11	Du Pont	Procedimiento para preparar composiciones de sulfonamida extruidas en pasta
GB2503416B (en) *	2012-04-20	2017-07-19	Rotam Agrochem Int Co Ltd	Method for spray tank cleanout
PL3851214T3 (pl) *	2012-05-01	2024-10-28	Monsanto Technology Llc	Sposób czyszczenia naczynia rolniczego z pozostałości pestycydu

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US2891855A (en)	1954-08-16	1959-06-23	Geigy Ag J R	Compositions and methods for influencing the growth of plants
US3060084A (en)	1961-06-09	1962-10-23	Du Pont	Improved homogeneous, readily dispersed, pesticidal concentrate
US3309192A (en)	1964-12-02	1967-03-14	Du Pont	Method of controlling seedling weed grasses
US4172714A (en)	1976-12-20	1979-10-30	E. I. Du Pont De Nemours And Company	Dry compactible, swellable herbicidal compositions and pellets produced therefrom
DE3246493A1 (de)	1982-12-16	1984-06-20	Bayer Ag, 5090 Leverkusen	Verfahren zur herstellung von wasserdispergierbaren granulaten
EP0124295B1 (en) *	1983-04-04	1991-04-03	E.I. Du Pont De Nemours And Company	Stabilized aqueous formulations of sulfonylureas
US4599412A (en) *	1983-11-23	1986-07-08	E. I. Du Pont De Nemours And Company	Process for preparation of sulfonylurea solution formulations
WO1989001477A1 (en) *	1987-08-19	1989-02-23	E.I. Du Pont De Nemours And Company	Process for preparing sulfonylurea salts

1993
- 1993-02-12 AU AU36187/93A patent/AU3618793A/en not_active Abandoned
- 1993-02-12 EP EP93905045A patent/EP0626807A1/en not_active Withdrawn
- 1993-02-12 JP JP5514907A patent/JPH07503973A/ja active Pending
- 1993-02-12 HU HU9402407A patent/HUT71707A/hu unknown
- 1993-02-12 WO PCT/US1993/001295 patent/WO1993016596A1/en not_active Ceased
- 1993-02-12 BR BR9305997A patent/BR9305997A/pt not_active Application Discontinuation
- 1993-02-12 RU RU94040706/04A patent/RU94040706A/ru unknown
- 1993-02-12 CA CA002130118A patent/CA2130118A1/en not_active Abandoned
- 1993-02-18 ZA ZA931139A patent/ZA931139B/xx unknown
- 1993-02-19 CN CN93101773A patent/CN1077838A/zh active Pending
- 1993-02-19 LT LTIP345A patent/LT3009B/lt not_active IP Right Cessation

Also Published As

Publication number	Publication date
CA2130118A1 (en)	1993-09-02
HU9402407D0 (en)	1994-11-28
AU3618793A (en)	1993-09-13
LT3009B (lt)	1994-08-25
CN1077838A (zh)	1993-11-03
RU94040706A (ru)	1996-07-10
BR9305997A (pt)	1997-10-21
WO1993016596A1 (en)	1993-09-02
JPH07503973A (ja)	1995-04-27
LTIP345A (lt)	1994-04-25
EP0626807A1 (en)	1994-12-07
ZA931139B (en)	1994-08-18

Legal Events

Date	Code	Title	Description
1997-06-30	DFC4	Cancellation of temporary prot. due to refusal

Publication	Publication Date	Title
EP0044809B1 (de)	1983-08-31	N-(2-substituierte Phenylsulfonyl)-N'-triazinylharnstoffe
EP0116518B1 (de)	1987-10-28	N-Phenylsulfonyl-N'-pyrimidinyl- und -triazinylharnstoffe
EP0496701B1 (de)	1996-03-06	Sulfonylharnstoffe als Herbizide
EP0807381B1 (de)	2000-03-15	Synergistische herbizide Mittel
IE60440B1 (en)	1994-07-13	Herbicidal pyridine sulfonamides
EP0204513A2 (en)	1986-12-10	Herbicidal sulfonamides
US5106872A (en)	1992-04-21	Pesticidal compositions with enhanced activity
BG51434A3 (bg)	1993-05-14	Хербицидно средство и метод за борба с нежелана растителност
HUT71707A (en)	1996-01-29	Method for lightening of cleanout spray tank
EP0122231B1 (de)	1990-01-17	Herbizides Mittel
AU2008243445B2 (en)	2013-10-03	Defoliant
KR970001777B1 (ko)	1997-02-15	제초제
WO1988004655A2 (en)	1988-06-30	Herbicidal pyridine sulfonamides
CA2867752C (en)	2021-03-16	Method for spray tank cleanout
WO1988004294A2 (en)	1988-06-16	Herbicidal aryloxybenzeneacetic acid derivatives
EP0206995A1 (de)	1986-12-30	N-Heterocyclosulfonyl-N'-pyrimidinyl-, N'-triazolyl- und N'-triazinyl-harnstoffe
EP0471646A2 (de)	1992-02-19	Sulfonylharnstoffe als Herbizide
EP0402316A1 (de)	1990-12-12	Sulfonylharnstoffe
US4604130A (en)	1986-08-05	Herbicidal N-[pyrimidine aminocarbonyl]isothiazole sulfonamides
EP0168264A2 (en)	1986-01-15	Herbicidal sulfonamides
EP0273860A1 (de)	1988-07-06	N-Heterocyclosulfonyl-N'-pyrimidinyl-, N-'-triazolyl- und N'-triazinylharnstoffe
US4917719A (en)	1990-04-17	Herbicidal isothiazole derivatives
EP0206772A2 (en)	1986-12-30	Herbicidal aryloxybenzeneacetic acid derivatives
EP0251998A2 (de)	1988-01-07	Neue Phenylsulfonylharnstoffe
JPS59205306A (ja)	1984-11-20	除草剤組成物およびその使用方法