CS250690B2 - Herbicide and plants' growing regulating agent and method of its efficient substance production - Google Patents

Herbicide and plants' growing regulating agent and method of its efficient substance production Download PDF

Info

Publication number: CS250690B2
Authority: CS; Czechoslovakia
Prior art keywords: complex; formula; cyclodextrin; benzenesulfonylurea; plants
Prior art date: 1984-06-08

Application number

CS854105A

Other languages

Czech (cs)

English (en)

Inventor

Gyoergy Matolcsy

Antal Gimesi

Krisztina Pelejtei

Janisz Sztatisz

Agota Tombor

Tibor Cserhati

Aniko Gerlei

Mariann Kardos

Jozsef Dukai

Dezsoe Seboek

Csaba Soeptei

Lajos Nagy

Ivan Belai

Original Assignee

Nitrokemia Ipartelepek

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.)

1984-06-08

Filing date

1985-06-07

Publication date

1987-05-14

1985-06-07 Application filed by Nitrokemia Ipartelepek filed Critical Nitrokemia Ipartelepek

1987-05-14 Publication of CS250690B2 publication Critical patent/CS250690B2/cs

Links

230000002363 herbicidal effect Effects 0.000 title claims abstract description 11
230000001105 regulatory effect Effects 0.000 title claims abstract description 9
238000000034 method Methods 0.000 title claims description 14
239000003795 chemical substances by application Substances 0.000 title claims description 5
238000004519 manufacturing process Methods 0.000 title abstract description 3
239000004009 herbicide Substances 0.000 title description 8
239000000126 substance Substances 0.000 title 1
239000000203 mixture Substances 0.000 claims abstract description 26
229920000858 Cyclodextrin Polymers 0.000 claims abstract description 19
230000008635 plant growth Effects 0.000 claims abstract description 11
WHGYBXFWUBPSRW-FOUAGVGXSA-N beta-cyclodextrin Chemical compound OC[C@H]([C@H]([C@@H]([C@H]1O)O)O[C@H]2O[C@@H]([C@@H](O[C@H]3O[C@H](CO)[C@H]([C@@H]([C@H]3O)O)O[C@H]3O[C@H](CO)[C@H]([C@@H]([C@H]3O)O)O[C@H]3O[C@H](CO)[C@H]([C@@H]([C@H]3O)O)O[C@H]3O[C@H](CO)[C@H]([C@@H]([C@H]3O)O)O3)[C@H](O)[C@H]2O)CO)O[C@@H]1O[C@H]1[C@H](O)[C@@H](O)[C@@H]3O[C@@H]1CO WHGYBXFWUBPSRW-FOUAGVGXSA-N 0.000 claims abstract description 9
235000011175 beta-cyclodextrine Nutrition 0.000 claims abstract description 9
GHDLZGOOOLEJKI-UHFFFAOYSA-N benzenesulfonylurea Chemical compound NC(=O)NS(=O)(=O)C1=CC=CC=C1 GHDLZGOOOLEJKI-UHFFFAOYSA-N 0.000 claims description 18
150000001875 compounds Chemical class 0.000 claims description 16
239000004480 active ingredient Substances 0.000 claims description 13
-1 4-methoxy-6-methyl-1,3,5-triazin-2-yl Chemical group 0.000 claims description 11
239000001116 FEMA 4028 Substances 0.000 claims description 8
229960004853 betadex Drugs 0.000 claims description 8
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 4
125000000217 alkyl group Chemical group 0.000 claims description 4
125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims description 4
229910052736 halogen Inorganic materials 0.000 claims description 3
150000002367 halogens Chemical group 0.000 claims description 3
229910052757 nitrogen Inorganic materials 0.000 claims description 3
125000003545 alkoxy group Chemical group 0.000 claims description 2
239000001257 hydrogen Substances 0.000 claims description 2
229910052739 hydrogen Inorganic materials 0.000 claims description 2
150000002431 hydrogen Chemical class 0.000 claims description 2
229940124530 sulfonamide Drugs 0.000 claims description 2
KHBQMWCZKVMBLN-UHFFFAOYSA-N Benzenesulfonamide Chemical compound NS(=O)(=O)C1=CC=CC=C1 KHBQMWCZKVMBLN-UHFFFAOYSA-N 0.000 claims 1
BVAPOGMQIPODIW-UHFFFAOYSA-N benzene;sulfonylurea Chemical class C1=CC=CC=C1.NC(=O)N=S(=O)=O BVAPOGMQIPODIW-UHFFFAOYSA-N 0.000 abstract 1
239000001202 beta-cyclodextrine Substances 0.000 abstract 1
241000196324 Embryophyta Species 0.000 description 17
238000000354 decomposition reaction Methods 0.000 description 16
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 16
238000012360 testing method Methods 0.000 description 10
HFHDHCJBZVLPGP-UHFFFAOYSA-N schardinger α-dextrin Chemical compound O1C(C(C2O)O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC(C(O)C2O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC2C(O)C(O)C1OC2CO HFHDHCJBZVLPGP-UHFFFAOYSA-N 0.000 description 7
239000013543 active substance Substances 0.000 description 6
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 6
239000000969 carrier Substances 0.000 description 5
YROXIXLRRCOBKF-UHFFFAOYSA-N sulfonylurea Chemical class OC(=N)N=S(=O)=O YROXIXLRRCOBKF-UHFFFAOYSA-N 0.000 description 5
239000004094 surface-active agent Substances 0.000 description 5
241000209140 Triticum Species 0.000 description 4
235000021307 Triticum Nutrition 0.000 description 4
238000002360 preparation method Methods 0.000 description 4
239000007858 starting material Substances 0.000 description 4
239000000725 suspension Substances 0.000 description 4
239000004563 wettable powder Substances 0.000 description 4
HFFXLYHRNRKAPM-UHFFFAOYSA-N 2,4,5-trichloro-n-(5-methyl-1,2-oxazol-3-yl)benzenesulfonamide Chemical compound O1C(C)=CC(NS(=O)(=O)C=2C(=CC(Cl)=C(Cl)C=2)Cl)=N1 HFFXLYHRNRKAPM-UHFFFAOYSA-N 0.000 description 3
239000005995 Aluminium silicate Substances 0.000 description 3
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
229940100389 Sulfonylurea Drugs 0.000 description 3
240000008042 Zea mays Species 0.000 description 3
235000012211 aluminium silicate Nutrition 0.000 description 3
239000003085 diluting agent Substances 0.000 description 3
230000000694 effects Effects 0.000 description 3
238000011156 evaluation Methods 0.000 description 3
NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 3
VYQNWZOUAUKGHI-UHFFFAOYSA-N monobenzone Chemical compound C1=CC(O)=CC=C1OCC1=CC=CC=C1 VYQNWZOUAUKGHI-UHFFFAOYSA-N 0.000 description 3
239000011541 reaction mixture Substances 0.000 description 3
239000002689 soil Substances 0.000 description 3
239000007787 solid Substances 0.000 description 3
239000000243 solution Substances 0.000 description 3
KMVZDSQHLDGKGV-UHFFFAOYSA-N 2-chlorobenzenesulfonyl chloride Chemical compound ClC1=CC=CC=C1S(Cl)(=O)=O KMVZDSQHLDGKGV-UHFFFAOYSA-N 0.000 description 2
USHHCQFIUMQAKY-UHFFFAOYSA-N 4-methoxy-6-methyl-1h-triazin-2-amine Chemical compound COC1=NN(N)NC(C)=C1 USHHCQFIUMQAKY-UHFFFAOYSA-N 0.000 description 2
235000006463 Brassica alba Nutrition 0.000 description 2
244000140786 Brassica hirta Species 0.000 description 2
235000011371 Brassica hirta Nutrition 0.000 description 2
IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
229920001214 Polysorbate 60 Polymers 0.000 description 2
235000015724 Trifolium pratense Nutrition 0.000 description 2
235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 2
235000002017 Zea mays subsp mays Nutrition 0.000 description 2
239000007864 aqueous solution Substances 0.000 description 2
238000006243 chemical reaction Methods 0.000 description 2
230000009918 complex formation Effects 0.000 description 2
239000012141 concentrate Substances 0.000 description 2
235000005822 corn Nutrition 0.000 description 2
235000014113 dietary fatty acids Nutrition 0.000 description 2
239000000194 fatty acid Substances 0.000 description 2
229930195729 fatty acid Natural products 0.000 description 2
125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
239000007788 liquid Substances 0.000 description 2
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 description 2
230000002688 persistence Effects 0.000 description 2
239000005648 plant growth regulator Substances 0.000 description 2
239000004476 plant protection product Substances 0.000 description 2
235000013526 red clover Nutrition 0.000 description 2
239000002904 solvent Substances 0.000 description 2
238000005507 spraying Methods 0.000 description 2
LSNNMFCWUKXFEE-UHFFFAOYSA-L sulfite Chemical compound [O-]S([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-L 0.000 description 2
238000002076 thermal analysis method Methods 0.000 description 2
239000002699 waste material Substances 0.000 description 2
LLKNJTUXPUNSHY-UHFFFAOYSA-N 1-(2-chlorophenyl)sulfonyl-3-(4,6-dimethylpyrimidin-2-yl)urea Chemical compound CC1=CC(C)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2)Cl)=N1 LLKNJTUXPUNSHY-UHFFFAOYSA-N 0.000 description 1
HMUNWXXNJPVALC-UHFFFAOYSA-N 1-[4-[2-(2,3-dihydro-1H-inden-2-ylamino)pyrimidin-5-yl]piperazin-1-yl]-2-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)ethanone Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)N1CCN(CC1)C(CN1CC2=C(CC1)NN=N2)=O HMUNWXXNJPVALC-UHFFFAOYSA-N 0.000 description 1
VSOOBQALJVLTBH-UHFFFAOYSA-N 2-aminosulfonyl-benzoic acid methyl ester Chemical compound COC(=O)C1=CC=CC=C1S(N)(=O)=O VSOOBQALJVLTBH-UHFFFAOYSA-N 0.000 description 1
235000021533 Beta vulgaris Nutrition 0.000 description 1
241000335053 Beta vulgaris Species 0.000 description 1
241000219310 Beta vulgaris subsp. vulgaris Species 0.000 description 1
ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 1
OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
239000005496 Chlorsulfuron Substances 0.000 description 1
XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
229920001353 Dextrin Polymers 0.000 description 1
239000004375 Dextrin Substances 0.000 description 1
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
241000209219 Hordeum Species 0.000 description 1
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 1
239000005909 Kieselgur Substances 0.000 description 1
241000209510 Liliopsida Species 0.000 description 1
FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
240000001140 Mimosa pudica Species 0.000 description 1
235000016462 Mimosa pudica Nutrition 0.000 description 1
244000088461 Panicum crus-galli Species 0.000 description 1
235000011999 Panicum crusgalli Nutrition 0.000 description 1
OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
240000003461 Setaria viridis Species 0.000 description 1
235000002248 Setaria viridis Nutrition 0.000 description 1
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
240000006394 Sorghum bicolor Species 0.000 description 1
235000011684 Sorghum saccharatum Nutrition 0.000 description 1
235000021536 Sugar beet Nutrition 0.000 description 1
240000002913 Trifolium pratense Species 0.000 description 1
244000098338 Triticum aestivum Species 0.000 description 1
235000007244 Zea mays Nutrition 0.000 description 1
HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
230000001154 acute effect Effects 0.000 description 1
125000001931 aliphatic group Chemical group 0.000 description 1
150000004996 alkyl benzenes Chemical class 0.000 description 1
150000003863 ammonium salts Chemical class 0.000 description 1
150000008064 anhydrides Chemical class 0.000 description 1
239000007900 aqueous suspension Substances 0.000 description 1
125000003118 aryl group Chemical group 0.000 description 1
KHBQMWCZKVMBLN-IDEBNGHGSA-N benzenesulfonamide Chemical group NS(=O)(=O)[13C]1=[13CH][13CH]=[13CH][13CH]=[13CH]1 KHBQMWCZKVMBLN-IDEBNGHGSA-N 0.000 description 1
229910052796 boron Inorganic materials 0.000 description 1
239000011575 calcium Substances 0.000 description 1
229910052791 calcium Inorganic materials 0.000 description 1
229910052799 carbon Inorganic materials 0.000 description 1
150000008280 chlorinated hydrocarbons Chemical class 0.000 description 1
239000000460 chlorine Substances 0.000 description 1
229910052801 chlorine Inorganic materials 0.000 description 1
230000001684 chronic effect Effects 0.000 description 1
239000010941 cobalt Substances 0.000 description 1
229910017052 cobalt Inorganic materials 0.000 description 1
GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
230000000536 complexating effect Effects 0.000 description 1
239000000356 contaminant Substances 0.000 description 1
238000011109 contamination Methods 0.000 description 1
230000001276 controlling effect Effects 0.000 description 1
239000010949 copper Substances 0.000 description 1
WUUZKBJEUBFVMV-UHFFFAOYSA-N copper molybdenum Chemical compound [Cu].[Mo] WUUZKBJEUBFVMV-UHFFFAOYSA-N 0.000 description 1
NGDNCZPCIZNCQS-UHFFFAOYSA-N ctk3j8699 Chemical compound Cl=S NGDNCZPCIZNCQS-UHFFFAOYSA-N 0.000 description 1
125000000753 cycloalkyl group Chemical group 0.000 description 1
HPXRVTGHNJAIIH-UHFFFAOYSA-N cyclohexanol Chemical compound OC1CCCCC1 HPXRVTGHNJAIIH-UHFFFAOYSA-N 0.000 description 1
230000006378 damage Effects 0.000 description 1
238000007865 diluting Methods 0.000 description 1
JMGZBMRVDHKMKB-UHFFFAOYSA-L disodium;2-sulfobutanedioate Chemical class [Na+].[Na+].OS(=O)(=O)C(C([O-])=O)CC([O-])=O JMGZBMRVDHKMKB-UHFFFAOYSA-L 0.000 description 1
239000002270 dispersing agent Substances 0.000 description 1
239000006185 dispersion Substances 0.000 description 1
238000004090 dissolution Methods 0.000 description 1
239000010459 dolomite Substances 0.000 description 1
229910000514 dolomite Inorganic materials 0.000 description 1
239000004495 emulsifiable concentrate Substances 0.000 description 1
239000003995 emulsifying agent Substances 0.000 description 1
230000001804 emulsifying effect Effects 0.000 description 1
239000000839 emulsion Substances 0.000 description 1
238000005516 engineering process Methods 0.000 description 1
VIBDJEWPNNCFQO-UHFFFAOYSA-N ethane-1,1,2-triol Chemical compound OCC(O)O VIBDJEWPNNCFQO-UHFFFAOYSA-N 0.000 description 1
241001233957 eudicotyledons Species 0.000 description 1
238000002474 experimental method Methods 0.000 description 1
150000004665 fatty acids Chemical class 0.000 description 1
150000002191 fatty alcohols Chemical class 0.000 description 1
230000002349 favourable effect Effects 0.000 description 1
239000000945 filler Substances 0.000 description 1
235000013305 food Nutrition 0.000 description 1
238000009472 formulation Methods 0.000 description 1
125000002791 glucosyl group Chemical group C1([C@H](O)[C@@H](O)[C@H](O)[C@H](O1)CO)* 0.000 description 1
239000008187 granular material Substances 0.000 description 1
239000005556 hormone Substances 0.000 description 1
229940088597 hormone Drugs 0.000 description 1
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
239000011261 inert gas Substances 0.000 description 1
239000000543 intermediate Substances 0.000 description 1
238000011835 investigation Methods 0.000 description 1
229910052742 iron Inorganic materials 0.000 description 1
239000011777 magnesium Substances 0.000 description 1
229910052749 magnesium Inorganic materials 0.000 description 1
WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 1
239000000463 material Substances 0.000 description 1
125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
125000001160 methoxycarbonyl group Chemical group [H]C([H])([H])OC(*)=O 0.000 description 1
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
239000002480 mineral oil Substances 0.000 description 1
235000010446 mineral oil Nutrition 0.000 description 1
125000004433 nitrogen atom Chemical group N* 0.000 description 1
229920001542 oligosaccharide Polymers 0.000 description 1
150000002482 oligosaccharides Chemical class 0.000 description 1
230000035515 penetration Effects 0.000 description 1
238000003359 percent control normalization Methods 0.000 description 1
230000002085 persistent effect Effects 0.000 description 1
239000011574 phosphorus Substances 0.000 description 1
229910052698 phosphorus Inorganic materials 0.000 description 1
231100000208 phytotoxic Toxicity 0.000 description 1
230000000885 phytotoxic effect Effects 0.000 description 1
239000002798 polar solvent Substances 0.000 description 1
239000011591 potassium Substances 0.000 description 1
229910052700 potassium Inorganic materials 0.000 description 1
239000000843 powder Substances 0.000 description 1
BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
239000011814 protection agent Substances 0.000 description 1
150000004760 silicates Chemical class 0.000 description 1
239000011734 sodium Substances 0.000 description 1
229910052708 sodium Inorganic materials 0.000 description 1
238000009331 sowing Methods 0.000 description 1
239000007921 spray Substances 0.000 description 1
150000003456 sulfonamides Chemical class 0.000 description 1
239000000454 talc Substances 0.000 description 1
229910052623 talc Inorganic materials 0.000 description 1
231100000419 toxicity Toxicity 0.000 description 1
230000001988 toxicity Effects 0.000 description 1
239000011573 trace mineral Substances 0.000 description 1
235000013619 trace mineral Nutrition 0.000 description 1
239000000080 wetting agent Substances 0.000 description 1
239000002023 wood Substances 0.000 description 1
239000011701 zinc Substances 0.000 description 1
229910052725 zinc Inorganic materials 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08B—POLYSACCHARIDES; DERIVATIVES THEREOF
- C08B37/00—Preparation of polysaccharides not provided for in groups C08B1/00 - C08B35/00; Derivatives thereof
- C08B37/0006—Homoglycans, i.e. polysaccharides having a main chain consisting of one single sugar, e.g. colominic acid
- C08B37/0009—Homoglycans, i.e. polysaccharides having a main chain consisting of one single sugar, e.g. colominic acid alpha-D-Glucans, e.g. polydextrose, alternan, glycogen; (alpha-1,4)(alpha-1,6)-D-Glucans; (alpha-1,3)(alpha-1,4)-D-Glucans, e.g. isolichenan or nigeran; (alpha-1,4)-D-Glucans; (alpha-1,3)-D-Glucans, e.g. pseudonigeran; Derivatives thereof
- C08B37/0012—Cyclodextrin [CD], e.g. cycle with 6 units (alpha), with 7 units (beta) and with 8 units (gamma), large-ring cyclodextrin or cycloamylose with 9 units or more; Derivatives thereof
- C08B37/0015—Inclusion compounds, i.e. host-guest compounds, e.g. polyrotaxanes
- 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

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Life Sciences & Earth Sciences (AREA)
Health & Medical Sciences (AREA)
Chemical & Material Sciences (AREA)
Engineering & Computer Science (AREA)
General Health & Medical Sciences (AREA)
Polymers & Plastics (AREA)
Plant Pathology (AREA)
Materials Engineering (AREA)
Chemical Kinetics & Catalysis (AREA)
Medicinal Chemistry (AREA)
Molecular Biology (AREA)
Organic Chemistry (AREA)
Agronomy & Crop Science (AREA)
Pest Control & Pesticides (AREA)
Biochemistry (AREA)
Dentistry (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)
Polysaccharides And Polysaccharide Derivatives (AREA)
Plural Heterocyclic Compounds (AREA)

CS854105A 1984-06-08 1985-06-07 Herbicide and plants' growing regulating agent and method of its efficient substance production CS250690B2 (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
HU842216A HU193933B (en)	1984-06-08	1984-06-08	Herbicide or plant growth stimulating agent comprising beta-cyclodextrin complex of benzolsulphonylurea derivative and process for preparing the active substances

Publications (1)

Publication Number	Publication Date
CS250690B2 true CS250690B2 (en)	1987-05-14

Family

ID=10958341

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CS854105A CS250690B2 (en)	1984-06-08	1985-06-07	Herbicide and plants' growing regulating agent and method of its efficient substance production

Country Status (25)

Country	Link
US (1)	US4672112A (fr)
JP (1)	JPS6156170A (fr)
AT (1)	AT391587B (fr)
AU (1)	AU573007B2 (fr)
BE (1)	BE902613A (fr)
BR (1)	BR8502710A (fr)
CA (1)	CA1263648A (fr)
CS (1)	CS250690B2 (fr)
DD (1)	DD234357A5 (fr)
DE (1)	DE3520725A1 (fr)
DK (1)	DK257985A (fr)
ES (1)	ES8604009A1 (fr)
FR (1)	FR2568877B1 (fr)
GR (1)	GR851379B (fr)
HU (1)	HU193933B (fr)
IL (1)	IL75391A0 (fr)
IT (1)	IT1206736B (fr)
NL (1)	NL8501638A (fr)
NZ (1)	NZ212337A (fr)
PL (1)	PL253824A1 (fr)
PT (1)	PT80605B (fr)
RO (1)	RO92012B (fr)
SE (1)	SE8502776L (fr)
SU (1)	SU1516002A3 (fr)
ZA (1)	ZA854234B (fr)

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GR1000748B (el) *	1989-08-07	1992-12-30	Basf Ag	Αποφυλλωτικο μεσο για τη βαμβακια.
FR2705963B1 (fr) *	1993-06-03	1995-07-13	Commissariat Energie Atomique	Dérivés sulfonés de cyclomalto-oligosaccharides, leur procédé de préparation et support de substances actives contenant ces dérivés.
US7737309B2 (en)	2004-07-13	2010-06-15	Nippon Soda Co., Ltd.	Clathrate compound, method for controlling concentration of aqueous agricultural chemical active ingredient solution, and agricultural chemical formulation
UA95310C2 (ru) *	2006-10-20	2011-07-25	Айкос Корпорейшен	Композиция, содержащая ингибитор chk1 и циклодекстрин, для лечения рака
EP2654433B1 (fr)	2010-12-21	2017-08-30	Bayer Cropscience LP	Les mutants "papier émeri" de bacillus et des méthodes d'application pour la promotion de la croissance des plantes, de la santé des plants et pour le contrôl des maladies et des parasites
JP5935976B2 (ja) *	2011-01-26	2016-06-15	日産化学工業株式会社	安定化される農薬固型製剤
MX2014002890A (es)	2011-09-12	2015-01-19	Bayer Cropscience Lp	Metodo para mejorar la salud y/o promover el crecimiento de una planta y/o mejorar la maduracion de frutos.
KR102569539B1 (ko) *	2016-11-07	2023-08-24	주식회사 에이치엘클레무브	차량용 물체감지시스템 및 차량용 물체감지방법

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US4169719A (en) *	1976-04-07	1979-10-02	E. I. Du Pont De Nemours And Co.	Herbicidal sulfonamides
CA1082189A (fr) *	1976-04-07	1980-07-22	George Levitt	Sulfamides herbicides
HU184066B (en) *	1979-12-28	1984-06-28	Chinoin Gyogyszer Es Vegyeszet	Plant growth regulating substance and process for preparing such compound
JPS57142962A (en) *	1981-02-28	1982-09-03	Santen Pharmaceut Co Ltd	Cyclodextrin clathrate compound of sulfur-containing compound
HU183430B (en) *	1981-05-12	1984-05-28	Chinoin Gyogyszer Es Vegyeszet	Process for producing cyclodextrine inclusion complexes of n-bracket-1-phenylethyl-bracket closed-3,3-diphenylpropylamine or n-bracket-1-phenylethyl-bracket closed-3,3-diphenylpropylamine-hydrochloride
BR8303322A (pt) *	1982-06-25	1984-02-07	Du Pont	Composto;composicao adequada e processo para controlar o crescimento de vegetacao indesejada
US4543120A (en) *	1982-08-12	1985-09-24	E. I. Du Pont De Nemours And Company	Alkyl sulfonyl sulfonamides
US4780125A (en) *	1982-09-01	1988-10-25	Ciba-Geigy Corporation	N-phenylsulfonyl-N'-triazinylureas
HU190818B (en) *	1982-11-09	1986-11-28	Chinoin Gyogyszer Es Vegyeszeti Termekek Gyara Rt,Hu	Process for producing complexes of piperonyl-butoxide-cyclodextrin

1984
- 1984-06-08 HU HU842216A patent/HU193933B/hu not_active IP Right Cessation
1985
- 1985-05-05 BR BR8502710A patent/BR8502710A/pt unknown
- 1985-06-03 IL IL75391A patent/IL75391A0/xx unknown
- 1985-06-04 ZA ZA854234A patent/ZA854234B/xx unknown
- 1985-06-05 AT AT0169985A patent/AT391587B/de not_active IP Right Cessation
- 1985-06-05 PL PL25382485A patent/PL253824A1/xx unknown
- 1985-06-05 PT PT80605A patent/PT80605B/pt unknown
- 1985-06-05 SE SE8502776A patent/SE8502776L/xx not_active Application Discontinuation
- 1985-06-06 NL NL8501638A patent/NL8501638A/nl not_active Application Discontinuation
- 1985-06-06 US US06/742,218 patent/US4672112A/en not_active Expired - Fee Related
- 1985-06-06 GR GR851379A patent/GR851379B/el unknown
- 1985-06-07 AU AU43421/85A patent/AU573007B2/en not_active Ceased
- 1985-06-07 IT IT8521067A patent/IT1206736B/it active
- 1985-06-07 BE BE0/215151A patent/BE902613A/fr not_active IP Right Cessation
- 1985-06-07 CS CS854105A patent/CS250690B2/cs unknown
- 1985-06-07 NZ NZ212337A patent/NZ212337A/xx unknown
- 1985-06-07 SU SU853912654A patent/SU1516002A3/ru active
- 1985-06-07 ES ES544005A patent/ES8604009A1/es not_active Expired
- 1985-06-07 RO RO119078A patent/RO92012B/ro unknown
- 1985-06-07 DK DK257985A patent/DK257985A/da not_active Application Discontinuation
- 1985-06-07 DD DD85277159A patent/DD234357A5/de unknown
- 1985-06-07 CA CA000483395A patent/CA1263648A/fr not_active Expired
- 1985-06-07 FR FR8508667A patent/FR2568877B1/fr not_active Expired
- 1985-06-08 JP JP60123533A patent/JPS6156170A/ja active Pending
- 1985-06-10 DE DE19853520725 patent/DE3520725A1/de active Granted

Also Published As

Publication number	Publication date
SU1516002A3 (ru)	1989-10-15
BR8502710A (pt)	1986-02-12
DK257985A (da)	1985-12-09
GR851379B (fr)	1985-11-25
CA1263648A (fr)	1989-12-05
PT80605A (en)	1985-07-01
RO92012A (fr)	1987-07-30
ES8604009A1 (es)	1986-01-16
AU4342185A (en)	1985-12-12
IL75391A0 (en)	1985-10-31
US4672112A (en)	1987-06-09
IT8521067A0 (it)	1985-06-07
FR2568877A1 (fr)	1986-02-14
DE3520725C2 (fr)	1988-06-16
JPS6156170A (ja)	1986-03-20
FR2568877B1 (fr)	1988-09-16
ATA169985A (de)	1990-05-15
HU193933B (en)	1987-12-28
PL253824A1 (en)	1986-09-23
SE8502776D0 (sv)	1985-06-05
AU573007B2 (en)	1988-05-26
DK257985D0 (da)	1985-06-07
DD234357A5 (de)	1986-04-02
DE3520725A1 (de)	1985-12-12
ZA854234B (en)	1986-01-29
AT391587B (de)	1990-10-25
PT80605B (en)	1987-01-15
BE902613A (fr)	1985-09-30
NZ212337A (en)	1988-10-28
ES544005A0 (es)	1986-01-16
NL8501638A (nl)	1986-01-02
RO92012B (ro)	1987-07-31
SE8502776L (sv)	1985-12-09
IT1206736B (it)	1989-05-03

Publication	Publication Date	Title
KR940001728B1 (ko)	1994-03-05	트리아진 유도체 및 그것을 유효성분으로 하는 제초제
EP0084020B1 (fr)	1987-09-16	Urées N-arylsulfonyle-N'-pyrimidinyle
RU2017734C1 (ru)	1994-08-15	Производные пиримидина, проявляющие гербицидную активность
EP0072347B1 (fr)	1985-11-13	N-Phénylsulfonyl-N'-pyrimidinyl- et -triazinyl-urées
PL156233B1 (en)	1992-02-28	Agent for fighting against harmflul insects or microorganisms or preventing an injurious attack by them
HU213362B (en)	1997-05-28	Herbicidal copositions containing n-/(1,3,5-triazine-2-yl)-carbamoyl/-benzol-sulfonamide derivatives and method for producing the active agents and for weed control
PL154960B1 (en)	1991-10-31	Agent for combating or preventing attack by insects or microorganisms
CS228935B2 (en)	1984-05-14	Herbicide and method of preparing active component thereof
PL170588B1 (en)	1997-01-31	Agrochemical sgent for fighting against growth of undersirable plants
Parus et al.	2020	Transformation of herbicides into dual function quaternary tropinium salts
EP0103537B1 (fr)	1987-07-08	N-arylsulfonyl-N'-triazolyl urées
US4672112A (en)	1987-06-09	β-Cyclodextrine complex of benzene sulphonyl urea derivatives
US4062896A (en)	1977-12-13	Nitro-diphenyl ethers
EP0068260B1 (fr)	1986-03-05	Phénoxypropionates substitués, procédé de préparation et utilisation comme herbicides
WO1991004964A1 (fr)	1991-04-18	Derives herbicides de sulfonamide
US5276007A (en)	1994-01-04	Herbicidal sulfonylureas
US4562210A (en)	1985-12-31	Bactericides
EP0270378A2 (fr)	1988-06-08	Dérivés d'acide aryloxyphényl acétique herbicides
GB2162529A (en)	1986-02-05	beta -Cyclodextrin complex of benzene sulphonyl urea derivatives
US3595639A (en)	1971-07-27	Triazinylamino substituted herbicides
NL8502820A (nl)	1986-05-16	Selectieve herbicidepreparaten met een verlengde werking, die als werkzaam bestanddeel alfa-chlooraceetamidederivaten bevatten.
US4256483A (en)	1981-03-17	2-Alkoxy pyridazinoquinazolinone derivatives as herbicides
US4211551A (en)	1980-07-08	Herbicide
JPS6327482A (ja)	1988-02-05	除草剤組成物
EP0101404A2 (fr)	1984-02-22	Esters organo-étain d'acides acyl-aminocarboxyliques et leur emploi comme pesticides