DD259342A5 - Pflanzenwachstumsregulierende mittel - Google Patents

Pflanzenwachstumsregulierende mittel Download PDF

Info

Publication number: DD259342A5
Authority: DD; German Democratic Republic
Prior art keywords: growth; compounds; plant growth; acid; phenyl
Prior art date: 1986-03-12

Application number

DD87300633A

Other languages

German (de)

English (en)

Inventor

Roland Schmierer

Reinhard Handte

Hilmar Mildenberger

Helmut Buerstell

Original Assignee

��@��k��

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1986-03-12

Filing date

1987-03-10

Publication date

1988-08-24

1987-03-10 Application filed by ��@��k�� filed Critical ��@��k��

1988-08-24 Publication of DD259342A5 publication Critical patent/DD259342A5/de

Links

239000003795 chemical substances by application Substances 0.000 claims abstract description 13
150000003839 salts Chemical class 0.000 claims abstract description 9
229910052736 halogen Inorganic materials 0.000 claims abstract description 4
150000002367 halogens Chemical class 0.000 claims abstract description 4
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims abstract description 3
125000006273 (C1-C3) alkyl group Chemical group 0.000 claims abstract 2
150000001875 compounds Chemical class 0.000 claims description 29
230000001105 regulatory effect Effects 0.000 claims description 3
230000008635 plant growth Effects 0.000 claims description 2
239000004606 Fillers/Extenders Substances 0.000 claims 1
239000004094 surface-active agent Substances 0.000 claims 1
239000004480 active ingredient Substances 0.000 abstract description 18
-1 R 2H Chemical group 0.000 abstract description 16
ZVKWLRUJGPDSMY-UHFFFAOYSA-N 1-phenylimidazole-2-carboxamide Chemical class NC(=O)C1=NC=CN1C1=CC=CC=C1 ZVKWLRUJGPDSMY-UHFFFAOYSA-N 0.000 abstract description 2
QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 11
241000196324 Embryophyta Species 0.000 description 11
239000000203 mixture Substances 0.000 description 11
238000009472 formulation Methods 0.000 description 8
239000000126 substance Substances 0.000 description 8
239000002253 acid Substances 0.000 description 7
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 6
230000012010 growth Effects 0.000 description 6
239000013543 active substance Substances 0.000 description 5
229910021529 ammonia Inorganic materials 0.000 description 5
230000000694 effects Effects 0.000 description 5
239000004495 emulsifiable concentrate Substances 0.000 description 5
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-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
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
239000000460 chlorine Substances 0.000 description 4
JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 4
239000003995 emulsifying agent Substances 0.000 description 4
239000008187 granular material Substances 0.000 description 4
230000009036 growth inhibition Effects 0.000 description 4
238000000034 method Methods 0.000 description 4
238000002156 mixing Methods 0.000 description 4
229920000151 polyglycol Polymers 0.000 description 4
239000010695 polyglycol Substances 0.000 description 4
239000000843 powder Substances 0.000 description 4
238000002360 preparation method Methods 0.000 description 4
229910052708 sodium Inorganic materials 0.000 description 4
239000011734 sodium Substances 0.000 description 4
239000007787 solid Substances 0.000 description 4
UDPGUMQDCGORJQ-UHFFFAOYSA-N (2-chloroethyl)phosphonic acid Chemical compound OP(O)(=O)CCCl UDPGUMQDCGORJQ-UHFFFAOYSA-N 0.000 description 3
239000005995 Aluminium silicate Substances 0.000 description 3
VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 3
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 3
241000209094 Oryza Species 0.000 description 3
125000000217 alkyl group Chemical group 0.000 description 3
235000012211 aluminium silicate Nutrition 0.000 description 3
239000006185 dispersion Substances 0.000 description 3
150000002191 fatty alcohols Chemical class 0.000 description 3
238000000227 grinding Methods 0.000 description 3
239000003630 growth substance Substances 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
239000000463 material Substances 0.000 description 3
239000005648 plant growth regulator Substances 0.000 description 3
239000002904 solvent Substances 0.000 description 3
239000005976 Ethephon Substances 0.000 description 2
ZHNUHDYFZUAESO-UHFFFAOYSA-N Formamide Chemical compound NC=O ZHNUHDYFZUAESO-UHFFFAOYSA-N 0.000 description 2
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
AFVFQIVMOAPDHO-UHFFFAOYSA-N Methanesulfonic acid Chemical compound CS(O)(=O)=O AFVFQIVMOAPDHO-UHFFFAOYSA-N 0.000 description 2
LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
235000007164 Oryza sativa Nutrition 0.000 description 2
GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 2
QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
150000007513 acids Chemical class 0.000 description 2
150000003863 ammonium salts Chemical class 0.000 description 2
238000005915 ammonolysis reaction Methods 0.000 description 2
238000009835 boiling Methods 0.000 description 2
239000000969 carrier Substances 0.000 description 2
239000012141 concentrate Substances 0.000 description 2
239000007859 condensation product Substances 0.000 description 2
235000014113 dietary fatty acids Nutrition 0.000 description 2
238000010410 dusting Methods 0.000 description 2
150000002170 ethers Chemical class 0.000 description 2
239000000194 fatty acid Substances 0.000 description 2
229930195729 fatty acid Natural products 0.000 description 2
239000003337 fertilizer Substances 0.000 description 2
239000000945 filler Substances 0.000 description 2
230000005764 inhibitory process Effects 0.000 description 2
239000007788 liquid Substances 0.000 description 2
239000002480 mineral oil Substances 0.000 description 2
150000003254 radicals Chemical class 0.000 description 2
239000011347 resin Substances 0.000 description 2
229920005989 resin Polymers 0.000 description 2
235000009566 rice Nutrition 0.000 description 2
238000005507 spraying Methods 0.000 description 2
KDYFGRWQOYBRFD-UHFFFAOYSA-N succinic acid Chemical compound OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 2
239000000454 talc Substances 0.000 description 2
229910052623 talc Inorganic materials 0.000 description 2
FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 description 2
238000009736 wetting Methods 0.000 description 2
DARPYRSDRJYGIF-PTNGSMBKSA-N (Z)-3-ethoxy-2-naphthalen-2-ylsulfonylprop-2-enenitrile Chemical compound C1=CC=CC2=CC(S(=O)(=O)C(\C#N)=C/OCC)=CC=C21 DARPYRSDRJYGIF-PTNGSMBKSA-N 0.000 description 1
CNGZUJQPNVPPCJ-UHFFFAOYSA-N 1-chloroethylphosphonic acid Chemical compound CC(Cl)P(O)(O)=O CNGZUJQPNVPPCJ-UHFFFAOYSA-N 0.000 description 1
SQAINHDHICKHLX-UHFFFAOYSA-N 1-naphthaldehyde Chemical class C1=CC=C2C(C=O)=CC=CC2=C1 SQAINHDHICKHLX-UHFFFAOYSA-N 0.000 description 1
FZJRVWGEDDPYOM-UHFFFAOYSA-N 1-phenylimidazole-2-carboxylic acid Chemical compound OC(=O)C1=NC=CN1C1=CC=CC=C1 FZJRVWGEDDPYOM-UHFFFAOYSA-N 0.000 description 1
XUJLWPFSUCHPQL-UHFFFAOYSA-N 11-methyldodecan-1-ol Chemical compound CC(C)CCCCCCCCCCO XUJLWPFSUCHPQL-UHFFFAOYSA-N 0.000 description 1
ZBNZAJFNDPPMDT-UHFFFAOYSA-N 1h-imidazole-5-carboxamide Chemical class NC(=O)C1=CNC=N1 ZBNZAJFNDPPMDT-UHFFFAOYSA-N 0.000 description 1
CMJUNAQINNWKAU-KTKRTIGZSA-N 2-[[(z)-2-oxononadec-10-enyl]amino]ethanesulfonic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)CNCCS(O)(=O)=O CMJUNAQINNWKAU-KTKRTIGZSA-N 0.000 description 1
PUAQLLVFLMYYJJ-UHFFFAOYSA-N 2-aminopropiophenone Chemical compound CC(N)C(=O)C1=CC=CC=C1 PUAQLLVFLMYYJJ-UHFFFAOYSA-N 0.000 description 1
METJMKLKGUXIGZ-UHFFFAOYSA-N 2-chloro-1,3-diethylbenzene Chemical compound CCC1=CC=CC(CC)=C1Cl METJMKLKGUXIGZ-UHFFFAOYSA-N 0.000 description 1
SVOAUHHKPGKPQK-UHFFFAOYSA-N 2-chloro-9-hydroxyfluorene-9-carboxylic acid Chemical compound C1=C(Cl)C=C2C(C(=O)O)(O)C3=CC=CC=C3C2=C1 SVOAUHHKPGKPQK-UHFFFAOYSA-N 0.000 description 1
NIOYEINNWHTIIM-UHFFFAOYSA-N 3-(2,6-diethylphenyl)imidazole-4-carboxylic acid Chemical compound CCC1=CC=CC(CC)=C1N1C(C(O)=O)=CN=C1 NIOYEINNWHTIIM-UHFFFAOYSA-N 0.000 description 1
FOGYNLXERPKEGN-UHFFFAOYSA-N 3-(2-hydroxy-3-methoxyphenyl)-2-[2-methoxy-4-(3-sulfopropyl)phenoxy]propane-1-sulfonic acid Chemical compound COC1=CC=CC(CC(CS(O)(=O)=O)OC=2C(=CC(CCCS(O)(=O)=O)=CC=2)OC)=C1O FOGYNLXERPKEGN-UHFFFAOYSA-N 0.000 description 1
QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonium chloride Substances [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 1
VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
229930192334 Auxin Natural products 0.000 description 1
240000002791 Brassica napus Species 0.000 description 1
235000004977 Brassica sinapistrum Nutrition 0.000 description 1
CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 1
BZZRPRJCFHGRPZ-UHFFFAOYSA-N CS(=O)(=O)OC1=C(C=CC=C1CC)CC Chemical compound CS(=O)(=O)OC1=C(C=CC=C1CC)CC BZZRPRJCFHGRPZ-UHFFFAOYSA-N 0.000 description 1
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
239000005974 Chlormequat Substances 0.000 description 1
102000004127 Cytokines Human genes 0.000 description 1
108090000695 Cytokines Proteins 0.000 description 1
240000005979 Hordeum vulgare Species 0.000 description 1
235000007340 Hordeum vulgare Nutrition 0.000 description 1
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
239000005909 Kieselgur Substances 0.000 description 1
BGRDGMRNKXEXQD-UHFFFAOYSA-N Maleic hydrazide Chemical compound OC1=CC=C(O)N=N1 BGRDGMRNKXEXQD-UHFFFAOYSA-N 0.000 description 1
OKIBNKKYNPBDRS-UHFFFAOYSA-N Mefluidide Chemical compound CC(=O)NC1=CC(NS(=O)(=O)C(F)(F)F)=C(C)C=C1C OKIBNKKYNPBDRS-UHFFFAOYSA-N 0.000 description 1
239000005984 Mepiquat Substances 0.000 description 1
229910002651 NO3 Inorganic materials 0.000 description 1
NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 1
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 1
241000209504 Poaceae Species 0.000 description 1
239000004372 Polyvinyl alcohol Substances 0.000 description 1
ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
229910004298 SiO 2 Inorganic materials 0.000 description 1
229920002125 Sokalan® Polymers 0.000 description 1
QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
239000004098 Tetracycline Substances 0.000 description 1
XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
239000000853 adhesive Substances 0.000 description 1
230000001070 adhesive effect Effects 0.000 description 1
230000000274 adsorptive effect Effects 0.000 description 1
125000001931 aliphatic group Chemical group 0.000 description 1
125000003342 alkenyl group Chemical group 0.000 description 1
125000003545 alkoxy group Chemical group 0.000 description 1
125000002877 alkyl aryl group Chemical group 0.000 description 1
235000011114 ammonium hydroxide Nutrition 0.000 description 1
HUTDUHSNJYTCAR-UHFFFAOYSA-N ancymidol Chemical compound C1=CC(OC)=CC=C1C(O)(C=1C=NC=NC=1)C1CC1 HUTDUHSNJYTCAR-UHFFFAOYSA-N 0.000 description 1
150000001450 anions Chemical class 0.000 description 1
239000002363 auxin Substances 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
WVDDGKGOMKODPV-UHFFFAOYSA-N benzyl alcohol Substances OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 description 1
239000011230 binding agent Substances 0.000 description 1
159000000007 calcium salts Chemical class 0.000 description 1
OOCMUZJPDXYRFD-UHFFFAOYSA-L calcium;2-dodecylbenzenesulfonate Chemical compound [Ca+2].CCCCCCCCCCCCC1=CC=CC=C1S([O-])(=O)=O.CCCCCCCCCCCCC1=CC=CC=C1S([O-])(=O)=O OOCMUZJPDXYRFD-UHFFFAOYSA-L 0.000 description 1
239000004202 carbamide Substances 0.000 description 1
150000001768 cations Chemical class 0.000 description 1
229910052801 chlorine Inorganic materials 0.000 description 1
JUZXDNPBRPUIOR-UHFFFAOYSA-N chlormequat Chemical compound C[N+](C)(C)CCCl JUZXDNPBRPUIOR-UHFFFAOYSA-N 0.000 description 1
239000000470 constituent Substances 0.000 description 1
125000004663 dialkyl amino group Chemical group 0.000 description 1
238000007865 diluting Methods 0.000 description 1
239000003085 diluting agent Substances 0.000 description 1
230000001804 emulsifying effect Effects 0.000 description 1
OAYLNYINCPYISS-UHFFFAOYSA-N ethyl acetate;hexane Chemical compound CCCCCC.CCOC(C)=O OAYLNYINCPYISS-UHFFFAOYSA-N 0.000 description 1
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
150000004665 fatty acids Chemical class 0.000 description 1
239000000417 fungicide Substances 0.000 description 1
239000007789 gas Substances 0.000 description 1
150000004676 glycans Chemical class 0.000 description 1
208000037824 growth disorder Diseases 0.000 description 1
239000003966 growth inhibitor Substances 0.000 description 1
238000003306 harvesting Methods 0.000 description 1
238000010438 heat treatment Methods 0.000 description 1
239000004009 herbicide Substances 0.000 description 1
229930195733 hydrocarbon Natural products 0.000 description 1
150000002430 hydrocarbons Chemical class 0.000 description 1
239000001257 hydrogen Substances 0.000 description 1
229910052739 hydrogen Inorganic materials 0.000 description 1
150000004693 imidazolium salts Chemical class 0.000 description 1
239000012442 inert solvent Substances 0.000 description 1
239000004615 ingredient Substances 0.000 description 1
FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
238000004519 manufacturing process Methods 0.000 description 1
238000002844 melting Methods 0.000 description 1
230000008018 melting Effects 0.000 description 1
NNCAWEWCFVZOGF-UHFFFAOYSA-N mepiquat Chemical compound C[N+]1(C)CCCCC1 NNCAWEWCFVZOGF-UHFFFAOYSA-N 0.000 description 1
230000004060 metabolic process Effects 0.000 description 1
229910052751 metal Inorganic materials 0.000 description 1
239000002184 metal Substances 0.000 description 1
229940098779 methanesulfonic acid Drugs 0.000 description 1
235000010446 mineral oil Nutrition 0.000 description 1
229920000847 nonoxynol Polymers 0.000 description 1
SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical class CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 1
239000003960 organic solvent Substances 0.000 description 1
230000000149 penetrating effect Effects 0.000 description 1
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
230000000885 phytotoxic effect Effects 0.000 description 1
239000003375 plant hormone Substances 0.000 description 1
239000004584 polyacrylic acid Substances 0.000 description 1
229920001522 polyglycol ester Polymers 0.000 description 1
229920001451 polypropylene glycol Polymers 0.000 description 1
229920001282 polysaccharide Polymers 0.000 description 1
239000005017 polysaccharide Substances 0.000 description 1
229920002451 polyvinyl alcohol Polymers 0.000 description 1
239000011591 potassium Substances 0.000 description 1
229910052700 potassium Inorganic materials 0.000 description 1
239000002244 precipitate Substances 0.000 description 1
239000010453 quartz Substances 0.000 description 1
230000026267 regulation of growth Effects 0.000 description 1
239000004576 sand Substances 0.000 description 1
229920005552 sodium lignosulfonate Polymers 0.000 description 1
RPACBEVZENYWOL-XFULWGLBSA-M sodium;(2r)-2-[6-(4-chlorophenoxy)hexyl]oxirane-2-carboxylate Chemical compound [Na+].C=1C=C(Cl)C=CC=1OCCCCCC[C@]1(C(=O)[O-])CO1 RPACBEVZENYWOL-XFULWGLBSA-M 0.000 description 1
238000003756 stirring Methods 0.000 description 1
238000003860 storage Methods 0.000 description 1
239000001384 succinic acid Substances 0.000 description 1
229960002180 tetracycline Drugs 0.000 description 1
229930101283 tetracycline Natural products 0.000 description 1
235000019364 tetracycline Nutrition 0.000 description 1
150000003522 tetracyclines Chemical class 0.000 description 1
YNJBWRMUSHSURL-UHFFFAOYSA-N trichloroacetic acid Chemical compound OC(=O)C(Cl)(Cl)Cl YNJBWRMUSHSURL-UHFFFAOYSA-N 0.000 description 1
GPRLSGONYQIRFK-MNYXATJNSA-N triton Chemical compound [3H+] GPRLSGONYQIRFK-MNYXATJNSA-N 0.000 description 1
230000009105 vegetative growth Effects 0.000 description 1
239000004563 wettable powder Substances 0.000 description 1
239000000080 wetting agent Substances 0.000 description 1
239000008096 xylene Substances 0.000 description 1

Classifications

- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
- A01N43/50—1,3-Diazoles; Hydrogenated 1,3-diazoles
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/66—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D233/90—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals

Landscapes

Life Sciences & Earth Sciences (AREA)
Organic Chemistry (AREA)
Chemical & Material Sciences (AREA)
Health & Medical Sciences (AREA)
Environmental Sciences (AREA)
Engineering & Computer Science (AREA)
Dentistry (AREA)
General Health & Medical Sciences (AREA)
Wood Science & Technology (AREA)
Zoology (AREA)
Plant Pathology (AREA)
Pest Control & Pesticides (AREA)
Agronomy & Crop Science (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Nitrogen Condensed Heterocyclic Rings (AREA)
Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

DD87300633A 1986-03-12 1987-03-10 Pflanzenwachstumsregulierende mittel DD259342A5 (de)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE19863608143 DE3608143A1 (de)	1986-03-12	1986-03-12	1-phenylimidazolcarbonsaeureamide, ihre herstellung sowie ihre verwendung als wachstumsregulatoren

Publications (1)

Publication Number	Publication Date
DD259342A5 true DD259342A5 (de)	1988-08-24

Family

ID=6296109

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
DD87300633A DD259342A5 (de)	1986-03-12	1987-03-10	Pflanzenwachstumsregulierende mittel

Country Status (16)

Country	Link
US (1)	US4755213A (fr)
EP (1)	EP0243615B1 (fr)
JP (1)	JPS62212374A (fr)
CN (1)	CN87101796A (fr)
AT (1)	ATE61800T1 (fr)
AU (1)	AU596829B2 (fr)
DD (1)	DD259342A5 (fr)
DE (2)	DE3608143A1 (fr)
DK (1)	DK124987A (fr)
ES (1)	ES2021621B3 (fr)
GR (1)	GR3001708T3 (fr)
HU (1)	HUT43241A (fr)
IL (1)	IL81840A0 (fr)
PH (1)	PH22674A (fr)
PT (1)	PT84467B (fr)
ZA (1)	ZA871757B (fr)

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE3627155A1 (de) *	1986-08-11	1988-02-18	Schering Ag	Imidazol-derivate
DE3902439A1 (de) *	1989-01-27	1990-08-02	Basf Ag	Pflanzenschuetzende mittel auf basis von 1-aryl- bzw. 1-hetarylimidazolcarbonsaeureestern
US5211737A (en) *	1989-01-31	1993-05-18	Basf Aktiengesellschaft	4-arryl-2-haloimidazole-5-carboxylic esters, the preparation and use thereof
US5223525A (en) *	1989-05-05	1993-06-29	Rhone-Poulenc Ag Company	Pesticidal 1-arylimidazoles
CZ284824B6 (cs) *	1989-05-05	1999-03-17	Rhone-Poulenc Agrochimie	1-Arylimidazoly, způsob jejich výroby a meziprodukty v tomto způsobu, prostředky, které je obsahují a jejich použití
CA2032289A1 (fr) *	1989-12-29	1991-06-30	Joseph A. Finkelstein	5-(alkyl)carboxamideimidazoles substitues
PE20141468A1 (es)	2010-12-21	2014-11-05	Bayer Cropscience Lp	Mutantes tipo papel de lija de bacillus y metodos de uso de los mismo para mejorar el crecimiento vegetal, promover la salud de plantas y controlar enfermedades y plagas
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.
CN102321027A (zh) *	2011-10-09	2012-01-18	中国药科大学	一种咪唑-4-甲酸酰胺类衍生物的制备方法

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE3217094A1 (de) *	1982-05-07	1983-11-10	Hoechst Ag, 6230 Frankfurt	1-substituierte imidazol-5-carbonsaeurederivate, ihre herstellung sowie ihre verwendung als biozide
EP0167776B1 (fr) *	1984-06-05	1989-04-05	Hoechst Aktiengesellschaft	Agent régulateur de la croissance des plantes
DE3444918A1 (de) *	1984-12-08	1986-06-12	Hoechst Ag, 6230 Frankfurt	1-phenyl-imidazol-5-carbonsaeure-derivate, ein verfahren zu ihrer herstellung und ihre verwendung als wachstumsregulatoren
DE3514116A1 (de) *	1985-04-19	1986-10-23	Hoechst Ag, 6230 Frankfurt	Neue cyclohexyl- und cyclohexenylimidazolverbindungen, verfahren zu ihrer herstellung und ihre verwendung als pflanzenwachstumsregulatoren

1986
- 1986-03-12 DE DE19863608143 patent/DE3608143A1/de not_active Withdrawn
1987
- 1987-03-03 EP EP87103004A patent/EP0243615B1/fr not_active Expired - Lifetime
- 1987-03-03 ES ES87103004T patent/ES2021621B3/es not_active Expired - Lifetime
- 1987-03-03 AT AT87103004T patent/ATE61800T1/de not_active IP Right Cessation
- 1987-03-03 DE DE8787103004T patent/DE3768697D1/de not_active Expired - Fee Related
- 1987-03-10 CN CN198787101796A patent/CN87101796A/zh active Pending
- 1987-03-10 IL IL81840A patent/IL81840A0/xx unknown
- 1987-03-10 US US07/024,357 patent/US4755213A/en not_active Expired - Fee Related
- 1987-03-10 DD DD87300633A patent/DD259342A5/de unknown
- 1987-03-10 JP JP62053202A patent/JPS62212374A/ja active Pending
- 1987-03-11 AU AU69894/87A patent/AU596829B2/en not_active Ceased
- 1987-03-11 ZA ZA871757A patent/ZA871757B/xx unknown
- 1987-03-11 HU HU871065A patent/HUT43241A/hu unknown
- 1987-03-11 PH PH35013A patent/PH22674A/en unknown
- 1987-03-11 DK DK124987A patent/DK124987A/da not_active Application Discontinuation
- 1987-03-12 PT PT84467A patent/PT84467B/pt unknown
1991
- 1991-04-02 GR GR91400421T patent/GR3001708T3/el unknown

Also Published As

Publication number	Publication date
AU6989487A (en)	1987-09-17
DE3608143A1 (de)	1987-09-17
ES2021621B3 (es)	1991-11-16
HUT43241A (en)	1987-10-28
AU596829B2 (en)	1990-05-17
EP0243615B1 (fr)	1991-03-20
DK124987A (da)	1987-09-13
EP0243615A2 (fr)	1987-11-04
PT84467B (en)	1989-03-31
CN87101796A (zh)	1987-09-23
ATE61800T1 (de)	1991-04-15
GR3001708T3 (en)	1992-11-23
DE3768697D1 (de)	1991-04-25
PT84467A (en)	1987-04-01
DK124987D0 (da)	1987-03-11
IL81840A0 (en)	1987-10-20
JPS62212374A (ja)	1987-09-18
PH22674A (en)	1988-11-14
EP0243615A3 (en)	1988-02-24
ZA871757B (en)	1987-09-01
US4755213A (en)	1988-07-05

Publication	Publication Date	Title
DE68916459T2 (de)	1994-10-13	Triazin-Herbizide.
DE2648008A1 (de)	1978-05-03	Acetanilide
EP0000940B1 (fr)	1980-08-06	Gamma-azolyl-alcools et leur utilisation comme régulateurs de croissance pour plantes
EP0011693A1 (fr)	1980-06-11	N-hétérocycles N-substitués par trifluorométhane-sulfonylaminophényle, leur préparation, compositions les contenant et leur utilisation pour la régulation de la croissance des plantes
DD261951A5 (de)	1988-11-16	Pflanzenwachstumsregulierende mittel
EP0003805A1 (fr)	1979-09-05	Pyridazones et compositions herbicides les contenant
EP0243615B1 (fr)	1991-03-20	Amides de phényl-1-imidazole-acide carbonique, leur procédé de préparation et leur application comme régulateurs de croissance
DE3514116A1 (de)	1986-10-23	Neue cyclohexyl- und cyclohexenylimidazolverbindungen, verfahren zu ihrer herstellung und ihre verwendung als pflanzenwachstumsregulatoren
EP0167776B1 (fr)	1989-04-05	Agent régulateur de la croissance des plantes
CH617833A5 (fr)	1980-06-30
DE2018969A1 (de)	1970-11-05	Selektive Herbizide
EP0075840B1 (fr)	1987-11-11	Phényléthers hétérocycliques, procédé pour leur préparation et herbicides les contenant
DE2738640A1 (de)	1978-03-02	Herbizide triazolyl -und imidazolylverbindungen
EP0001751B1 (fr)	1980-09-17	Dérivés de N-(imidazolylméthyle)-acétanilide, leur application comme herbicides et procédé pour combattre la croissance de plantes indésirables
DD259124A5 (de)	1988-08-17	Pflanzenwachstumsregulierende mittel
DE3444918A1 (de)	1986-06-12	1-phenyl-imidazol-5-carbonsaeure-derivate, ein verfahren zu ihrer herstellung und ihre verwendung als wachstumsregulatoren
DD218828A5 (de)	1985-02-20	Herbizide zusammensetzung
DE3120859A1 (de)	1982-12-23	Dihalogenacetamide, verfahren zu ihrer herstellung und herbizide mittel, die acetanilide als herbizide wirkstoffe und diese dihalogenacetamide als antagonistische mittel enthalten
DE3883423T2 (de)	1994-01-05	Oximino-Äther-Verbindungen.
DD203454A5 (de)	1983-10-26	Herbizides mittel
DD262992A5 (de)	1988-12-21	Nematizide und insektizide zusammensetzung
DE68918200T2 (de)	1995-03-09	2,6-Substituierte 1,2- oder 1,6-Dihydropyridin-Derivate.
EP0013873A1 (fr)	1980-08-06	Anilides de l'acide N-azolyl acétique, procédé pour leur préparation et leur utilisation comme herbicides
DE2832890A1 (de)	1980-02-14	Herbizide mittel
CH638794A5 (de)	1983-10-14	Herbizid wirksame 1,2,4-triazin-5-onderivate.