DE2639711A1 - Verwendung von dinitroanilinderivaten zur unterdrueckung des wachstums von trieben, zweigen und sproesslingen an pflanzen - Google Patents
Verwendung von dinitroanilinderivaten zur unterdrueckung des wachstums von trieben, zweigen und sproesslingen an pflanzenInfo
- Publication number
- DE2639711A1 DE2639711A1 DE19762639711 DE2639711A DE2639711A1 DE 2639711 A1 DE2639711 A1 DE 2639711A1 DE 19762639711 DE19762639711 DE 19762639711 DE 2639711 A DE2639711 A DE 2639711A DE 2639711 A1 DE2639711 A1 DE 2639711A1
- Authority
- DE
- Germany
- Prior art keywords
- plants
- use according
- growth
- shoots
- compounds
- 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.)
- Pending
Links
- 230000012010 growth Effects 0.000 title claims description 34
- LZGUHMNOBNWABZ-UHFFFAOYSA-N n-nitro-n-phenylnitramide Chemical class [O-][N+](=O)N([N+]([O-])=O)C1=CC=CC=C1 LZGUHMNOBNWABZ-UHFFFAOYSA-N 0.000 title description 6
- 150000001875 compounds Chemical class 0.000 claims description 29
- QFUSCYRJMXLNRB-UHFFFAOYSA-N 2,6-dinitroaniline Chemical class NC1=C([N+]([O-])=O)C=CC=C1[N+]([O-])=O QFUSCYRJMXLNRB-UHFFFAOYSA-N 0.000 claims description 11
- 235000013399 edible fruits Nutrition 0.000 claims description 9
- 230000017260 vegetative to reproductive phase transition of meristem Effects 0.000 claims description 6
- 239000004480 active ingredient Substances 0.000 claims description 4
- 231100000208 phytotoxic Toxicity 0.000 claims description 3
- 230000000885 phytotoxic effect Effects 0.000 claims description 3
- 239000002023 wood Substances 0.000 claims description 3
- 238000007598 dipping method Methods 0.000 claims description 2
- 238000003306 harvesting Methods 0.000 claims description 2
- 238000005507 spraying Methods 0.000 claims description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 2
- 241000196324 Embryophyta Species 0.000 description 39
- 239000000243 solution Substances 0.000 description 18
- 239000000080 wetting agent Substances 0.000 description 13
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 9
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 9
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 8
- 239000000203 mixture Substances 0.000 description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
- 239000003795 chemical substances by application Substances 0.000 description 7
- 235000002629 Acer saccharinum Nutrition 0.000 description 6
- 244000046139 Acer saccharum Species 0.000 description 6
- 235000004421 Acer saccharum Nutrition 0.000 description 6
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 6
- 241001149163 Ulmus americana Species 0.000 description 6
- 238000000034 method Methods 0.000 description 6
- 239000000126 substance Substances 0.000 description 6
- 230000001629 suppression Effects 0.000 description 6
- FRFMLDNFLXIDSH-UHFFFAOYSA-N 5-tert-butyl-2-chloro-1,3-dinitrobenzene Chemical compound CC(C)(C)C1=CC([N+]([O-])=O)=C(Cl)C([N+]([O-])=O)=C1 FRFMLDNFLXIDSH-UHFFFAOYSA-N 0.000 description 5
- 241000234282 Allium Species 0.000 description 5
- 235000002732 Allium cepa var. cepa Nutrition 0.000 description 5
- SPNQRCTZKIBOAX-UHFFFAOYSA-N Butralin Chemical compound CCC(C)NC1=C([N+]([O-])=O)C=C(C(C)(C)C)C=C1[N+]([O-])=O SPNQRCTZKIBOAX-UHFFFAOYSA-N 0.000 description 5
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 4
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
- 241001536352 Fraxinus americana Species 0.000 description 4
- 244000061456 Solanum tuberosum Species 0.000 description 4
- 235000002595 Solanum tuberosum Nutrition 0.000 description 4
- 150000001412 amines Chemical class 0.000 description 4
- 238000011156 evaluation Methods 0.000 description 4
- 210000003746 feather Anatomy 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- 238000002360 preparation method Methods 0.000 description 4
- 239000007921 spray Substances 0.000 description 4
- FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- 235000011430 Malus pumila Nutrition 0.000 description 3
- 244000070406 Malus silvestris Species 0.000 description 3
- 235000015103 Malus silvestris Nutrition 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- 239000007864 aqueous solution Substances 0.000 description 3
- 244000052616 bacterial pathogen Species 0.000 description 3
- -1 fatty acid esters Chemical class 0.000 description 3
- NJBDTWSOYUZQPM-UHFFFAOYSA-N 4-tert-butyl-2,6-dinitrophenol Chemical compound CC(C)(C)C1=CC([N+]([O-])=O)=C(O)C([N+]([O-])=O)=C1 NJBDTWSOYUZQPM-UHFFFAOYSA-N 0.000 description 2
- 240000004731 Acer pseudoplatanus Species 0.000 description 2
- 235000002754 Acer pseudoplatanus Nutrition 0.000 description 2
- 244000144730 Amygdalus persica Species 0.000 description 2
- ROSDSFDQCJNGOL-UHFFFAOYSA-N Dimethylamine Chemical compound CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 description 2
- QUSNBJAOOMFDIB-UHFFFAOYSA-N Ethylamine Chemical compound CCN QUSNBJAOOMFDIB-UHFFFAOYSA-N 0.000 description 2
- BAVYZALUXZFZLV-UHFFFAOYSA-N Methylamine Chemical compound NC BAVYZALUXZFZLV-UHFFFAOYSA-N 0.000 description 2
- 235000006040 Prunus persica var persica Nutrition 0.000 description 2
- 229960000583 acetic acid Drugs 0.000 description 2
- 150000001408 amides Chemical class 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 238000011161 development Methods 0.000 description 2
- 230000018109 developmental process Effects 0.000 description 2
- 235000014113 dietary fatty acids Nutrition 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000000194 fatty acid Substances 0.000 description 2
- 229930195729 fatty acid Natural products 0.000 description 2
- 230000002349 favourable effect Effects 0.000 description 2
- 239000012362 glacial acetic acid Substances 0.000 description 2
- 230000005484 gravity Effects 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 230000006911 nucleation Effects 0.000 description 2
- 238000010899 nucleation Methods 0.000 description 2
- 235000014571 nuts Nutrition 0.000 description 2
- 235000012015 potatoes Nutrition 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- CGNBQYFXGQHUQP-UHFFFAOYSA-N 2,3-dinitroaniline Chemical class NC1=CC=CC([N+]([O-])=O)=C1[N+]([O-])=O CGNBQYFXGQHUQP-UHFFFAOYSA-N 0.000 description 1
- ZOAHSRMVOVANIX-UHFFFAOYSA-N 2,6-dinitro-n-pentan-3-ylaniline Chemical compound CCC(CC)NC1=C([N+]([O-])=O)C=CC=C1[N+]([O-])=O ZOAHSRMVOVANIX-UHFFFAOYSA-N 0.000 description 1
- WPQDXNWIGNCODE-UHFFFAOYSA-N 2,6-dinitro-n-propan-2-ylaniline Chemical compound CC(C)NC1=C([N+]([O-])=O)C=CC=C1[N+]([O-])=O WPQDXNWIGNCODE-UHFFFAOYSA-N 0.000 description 1
- KWVPFECTOKLOBL-KTKRTIGZSA-N 2-[(z)-octadec-9-enoxy]ethanol Chemical compound CCCCCCCC\C=C/CCCCCCCCOCCO KWVPFECTOKLOBL-KTKRTIGZSA-N 0.000 description 1
- XPZLLPFKCUQXFB-UHFFFAOYSA-N 4-butyl-2,6-dinitroaniline Chemical compound CCCCC1=CC([N+]([O-])=O)=C(N)C([N+]([O-])=O)=C1 XPZLLPFKCUQXFB-UHFFFAOYSA-N 0.000 description 1
- MOOOPNRPJGZXPE-UHFFFAOYSA-N 4-methyl-2,6-dinitroaniline Chemical compound CC1=CC([N+]([O-])=O)=C(N)C([N+]([O-])=O)=C1 MOOOPNRPJGZXPE-UHFFFAOYSA-N 0.000 description 1
- 125000004920 4-methyl-2-pentyl group Chemical group CC(CC(C)*)C 0.000 description 1
- CUTHFSYWMSPYOS-UHFFFAOYSA-N 4-tert-butyl-2,6-dinitroaniline Chemical class CC(C)(C)C1=CC([N+]([O-])=O)=C(N)C([N+]([O-])=O)=C1 CUTHFSYWMSPYOS-UHFFFAOYSA-N 0.000 description 1
- PSEIWGPKFWRHOR-UHFFFAOYSA-N 4-tert-butyl-n-ethyl-2,6-dinitroaniline Chemical compound CCNC1=C([N+]([O-])=O)C=C(C(C)(C)C)C=C1[N+]([O-])=O PSEIWGPKFWRHOR-UHFFFAOYSA-N 0.000 description 1
- QHPQWRBYOIRBIT-UHFFFAOYSA-N 4-tert-butylphenol Chemical compound CC(C)(C)C1=CC=C(O)C=C1 QHPQWRBYOIRBIT-UHFFFAOYSA-N 0.000 description 1
- QCVGEOXPDFCNHA-UHFFFAOYSA-N 5,5-dimethyl-2,4-dioxo-1,3-oxazolidine-3-carboxamide Chemical compound CC1(C)OC(=O)N(C(N)=O)C1=O QCVGEOXPDFCNHA-UHFFFAOYSA-N 0.000 description 1
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 1
- 241000208140 Acer Species 0.000 description 1
- 235000006667 Aleurites moluccana Nutrition 0.000 description 1
- 235000011446 Amygdalus persica Nutrition 0.000 description 1
- 235000000832 Ayote Nutrition 0.000 description 1
- 241000219310 Beta vulgaris subsp. vulgaris Species 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- 244000068645 Carya illinoensis Species 0.000 description 1
- 235000009025 Carya illinoensis Nutrition 0.000 description 1
- 240000009226 Corylus americana Species 0.000 description 1
- 235000001543 Corylus americana Nutrition 0.000 description 1
- 235000007466 Corylus avellana Nutrition 0.000 description 1
- 241000219122 Cucurbita Species 0.000 description 1
- 235000009854 Cucurbita moschata Nutrition 0.000 description 1
- 235000009804 Cucurbita pepo subsp pepo Nutrition 0.000 description 1
- 102000002322 Egg Proteins Human genes 0.000 description 1
- 108010000912 Egg Proteins Proteins 0.000 description 1
- 240000007049 Juglans regia Species 0.000 description 1
- 235000009496 Juglans regia Nutrition 0.000 description 1
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 240000007930 Oxalis acetosella Species 0.000 description 1
- 235000008098 Oxalis acetosella Nutrition 0.000 description 1
- 240000007377 Petunia x hybrida Species 0.000 description 1
- 235000010627 Phaseolus vulgaris Nutrition 0.000 description 1
- 244000046052 Phaseolus vulgaris Species 0.000 description 1
- 235000006485 Platanus occidentalis Nutrition 0.000 description 1
- 241001290151 Prunus avium subsp. avium Species 0.000 description 1
- 240000005809 Prunus persica Species 0.000 description 1
- 241000219492 Quercus Species 0.000 description 1
- 240000004885 Quercus rubra Species 0.000 description 1
- 235000009135 Quercus rubra Nutrition 0.000 description 1
- KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-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
- 241000736851 Tagetes Species 0.000 description 1
- 235000012308 Tagetes Nutrition 0.000 description 1
- 235000021307 Triticum Nutrition 0.000 description 1
- 244000098338 Triticum aestivum Species 0.000 description 1
- 229920004890 Triton X-100 Polymers 0.000 description 1
- 239000013504 Triton X-100 Substances 0.000 description 1
- 235000014787 Vitis vinifera Nutrition 0.000 description 1
- 240000006365 Vitis vinifera Species 0.000 description 1
- 240000008042 Zea mays Species 0.000 description 1
- 235000016383 Zea mays subsp huehuetenangensis Nutrition 0.000 description 1
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
- 229940045714 alkyl sulfonate alkylating agent Drugs 0.000 description 1
- 150000008052 alkyl sulfonates Chemical class 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 239000002518 antifoaming agent Substances 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 239000012876 carrier material Substances 0.000 description 1
- 235000013339 cereals Nutrition 0.000 description 1
- 235000019693 cherries Nutrition 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 235000008504 concentrate Nutrition 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000005520 cutting process Methods 0.000 description 1
- FMABSXTZZMCAFE-UHFFFAOYSA-N decan-1-ol Chemical compound CCCCCCCCCCO.CCCCCCCCCCO FMABSXTZZMCAFE-UHFFFAOYSA-N 0.000 description 1
- 230000006735 deficit Effects 0.000 description 1
- 230000001934 delay Effects 0.000 description 1
- 229910003460 diamond Inorganic materials 0.000 description 1
- 239000010432 diamond Substances 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 235000014103 egg white Nutrition 0.000 description 1
- 210000000969 egg white Anatomy 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 235000013312 flour Nutrition 0.000 description 1
- 239000000417 fungicide Substances 0.000 description 1
- 150000002314 glycerols Chemical class 0.000 description 1
- 239000012456 homogeneous solution Substances 0.000 description 1
- 238000003898 horticulture Methods 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 239000002917 insecticide Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 235000014666 liquid concentrate Nutrition 0.000 description 1
- 235000009973 maize Nutrition 0.000 description 1
- DJQIRIBTOYBTHL-UHFFFAOYSA-N n,4-diethyl-2,6-dinitroaniline Chemical compound CCNC1=C([N+]([O-])=O)C=C(CC)C=C1[N+]([O-])=O DJQIRIBTOYBTHL-UHFFFAOYSA-N 0.000 description 1
- MDXPRXYGYOMMKQ-UHFFFAOYSA-N n-butan-2-yl-2,6-dinitroaniline Chemical compound CCC(C)NC1=C([N+]([O-])=O)C=CC=C1[N+]([O-])=O MDXPRXYGYOMMKQ-UHFFFAOYSA-N 0.000 description 1
- BTLJAAKRVATXTR-UHFFFAOYSA-N n-heptan-2-yl-4-methyl-2,6-dinitroaniline Chemical compound CCCCCC(C)NC1=C([N+]([O-])=O)C=C(C)C=C1[N+]([O-])=O BTLJAAKRVATXTR-UHFFFAOYSA-N 0.000 description 1
- PJHYNWVLFKBSAM-UHFFFAOYSA-N n-methyl-2,6-dinitro-4-propan-2-ylaniline Chemical compound CNC1=C([N+]([O-])=O)C=C(C(C)C)C=C1[N+]([O-])=O PJHYNWVLFKBSAM-UHFFFAOYSA-N 0.000 description 1
- 229910017604 nitric acid Inorganic materials 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 235000011837 pasties Nutrition 0.000 description 1
- 125000002467 phosphate group Chemical class [H]OP(=O)(O[H])O[*] 0.000 description 1
- 230000008635 plant growth Effects 0.000 description 1
- 235000014483 powder concentrate Nutrition 0.000 description 1
- XOFYZVNMUHMLCC-ZPOLXVRWSA-N prednisone Chemical compound O=C1C=C[C@]2(C)[C@H]3C(=O)C[C@](C)([C@@](CC4)(O)C(=O)CO)[C@@H]4[C@@H]3CCC2=C1 XOFYZVNMUHMLCC-ZPOLXVRWSA-N 0.000 description 1
- 235000015136 pumpkin Nutrition 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- BHRZNVHARXXAHW-UHFFFAOYSA-N sec-butylamine Chemical compound CCC(C)N BHRZNVHARXXAHW-UHFFFAOYSA-N 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 238000010561 standard procedure Methods 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 1
- GPRLSGONYQIRFK-MNYXATJNSA-N triton Chemical compound [3H+] GPRLSGONYQIRFK-MNYXATJNSA-N 0.000 description 1
- 230000004222 uncontrolled growth Effects 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 239000011345 viscous material Substances 0.000 description 1
- 239000004563 wettable powder Substances 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C201/00—Preparation of esters of nitric or nitrous acid or of compounds containing nitro or nitroso groups bound to a carbon skeleton
- C07C201/06—Preparation of nitro compounds
- C07C201/12—Preparation of nitro compounds by reactions not involving the formation of nitro groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C209/00—Preparation of compounds containing amino groups bound to a carbon skeleton
- C07C209/04—Preparation of compounds containing amino groups bound to a carbon skeleton by substitution of functional groups by amino groups
- C07C209/06—Preparation of compounds containing amino groups bound to a carbon skeleton by substitution of functional groups by amino groups by substitution of halogen atoms
- C07C209/10—Preparation of compounds containing amino groups bound to a carbon skeleton by substitution of functional groups by amino groups by substitution of halogen atoms with formation of amino groups bound to carbon atoms of six-membered aromatic rings or from amines having nitrogen atoms bound to carbon atoms of six-membered aromatic rings
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US61048375A | 1975-09-04 | 1975-09-04 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE2639711A1 true DE2639711A1 (de) | 1977-03-17 |
Family
ID=24445187
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE19762639711 Pending DE2639711A1 (de) | 1975-09-04 | 1976-09-03 | Verwendung von dinitroanilinderivaten zur unterdrueckung des wachstums von trieben, zweigen und sproesslingen an pflanzen |
Country Status (5)
| Country | Link |
|---|---|
| BE (1) | BE845818A (enrdf_load_stackoverflow) |
| DE (1) | DE2639711A1 (enrdf_load_stackoverflow) |
| FR (1) | FR2322540A1 (enrdf_load_stackoverflow) |
| NL (1) | NL7609827A (enrdf_load_stackoverflow) |
| ZA (1) | ZA765191B (enrdf_load_stackoverflow) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2671942A1 (fr) * | 1991-01-29 | 1992-07-31 | Produits Ind Cie Fse | Produit anti-bourgeons pour la vigne et d'autres vegetaux ligneux et procede pour sa mise en óoeuvre. |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NL7016382A (enrdf_load_stackoverflow) * | 1969-11-20 | 1971-05-24 | Autoelektronik Ag |
-
1976
- 1976-08-30 ZA ZA765191A patent/ZA765191B/xx unknown
- 1976-09-03 DE DE19762639711 patent/DE2639711A1/de active Pending
- 1976-09-03 BE BE170319A patent/BE845818A/xx unknown
- 1976-09-03 NL NL7609827A patent/NL7609827A/xx not_active Application Discontinuation
- 1976-09-03 FR FR7626688A patent/FR2322540A1/fr active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| BE845818A (fr) | 1976-12-31 |
| ZA765191B (en) | 1977-08-31 |
| FR2322540B1 (enrdf_load_stackoverflow) | 1978-11-03 |
| FR2322540A1 (fr) | 1977-04-01 |
| NL7609827A (nl) | 1977-03-08 |
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