JPS595103A - 場合によつては置換されたチオメチル−シクロアルキルアミノ−ｓ−トリアジンを含有する選択的除草剤 - Google Patents
場合によつては置換されたチオメチル−シクロアルキルアミノ−ｓ−トリアジンを含有する選択的除草剤Info
- Publication number
- JPS595103A JPS595103A JP58102984A JP10298483A JPS595103A JP S595103 A JPS595103 A JP S595103A JP 58102984 A JP58102984 A JP 58102984A JP 10298483 A JP10298483 A JP 10298483A JP S595103 A JPS595103 A JP S595103A
- Authority
- JP
- Japan
- Prior art keywords
- group
- methylthio
- selective herbicide
- triazine
- weeds
- 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
- 239000004009 herbicide Substances 0.000 title claims description 15
- 230000002363 herbicidal effect Effects 0.000 title claims description 12
- 241000196324 Embryophyta Species 0.000 claims description 31
- 239000013543 active substance Substances 0.000 claims description 12
- 239000000203 mixture Substances 0.000 claims description 8
- 125000001424 substituent group Chemical group 0.000 claims description 6
- 239000000126 substance Substances 0.000 claims description 5
- 240000007594 Oryza sativa Species 0.000 claims description 4
- 235000007164 Oryza sativa Nutrition 0.000 claims description 4
- 125000000217 alkyl group Chemical group 0.000 claims description 4
- 235000009566 rice Nutrition 0.000 claims description 4
- 239000002904 solvent Substances 0.000 claims description 4
- 239000003337 fertilizer Substances 0.000 claims description 3
- 239000000853 adhesive Substances 0.000 claims description 2
- 230000001070 adhesive effect Effects 0.000 claims description 2
- 125000004183 alkoxy alkyl group Chemical group 0.000 claims description 2
- 125000003545 alkoxy group Chemical group 0.000 claims description 2
- 239000012752 auxiliary agent Substances 0.000 claims description 2
- 125000004432 carbon atom Chemical group C* 0.000 claims description 2
- 239000003085 diluting agent Substances 0.000 claims description 2
- 239000002270 dispersing agent Substances 0.000 claims description 2
- 239000003995 emulsifying agent Substances 0.000 claims description 2
- 239000000417 fungicide Substances 0.000 claims description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 2
- 229910052500 inorganic mineral Inorganic materials 0.000 claims description 2
- 239000002917 insecticide Substances 0.000 claims description 2
- 239000011707 mineral Substances 0.000 claims description 2
- 244000045561 useful plants Species 0.000 claims description 2
- 239000000080 wetting agent Substances 0.000 claims description 2
- 239000000654 additive Substances 0.000 claims 1
- 230000000996 additive effect Effects 0.000 claims 1
- 239000000969 carrier Substances 0.000 claims 1
- 230000004083 survival effect Effects 0.000 claims 1
- 150000001875 compounds Chemical class 0.000 description 32
- 238000011282 treatment Methods 0.000 description 13
- 230000000694 effects Effects 0.000 description 11
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 10
- 238000000034 method Methods 0.000 description 10
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 9
- 235000013339 cereals Nutrition 0.000 description 8
- 241000209140 Triticum Species 0.000 description 7
- 235000021307 Triticum Nutrition 0.000 description 7
- 241001148683 Zostera marina Species 0.000 description 7
- 230000000052 comparative effect Effects 0.000 description 7
- 240000004731 Acer pseudoplatanus Species 0.000 description 6
- 235000002754 Acer pseudoplatanus Nutrition 0.000 description 6
- 235000006485 Platanus occidentalis Nutrition 0.000 description 6
- 244000075850 Avena orientalis Species 0.000 description 5
- 229920000742 Cotton Polymers 0.000 description 5
- 244000068988 Glycine max Species 0.000 description 5
- 235000010469 Glycine max Nutrition 0.000 description 5
- 244000299507 Gossypium hirsutum Species 0.000 description 5
- 241000209219 Hordeum Species 0.000 description 5
- 238000003756 stirring Methods 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- 240000003173 Drymaria cordata Species 0.000 description 4
- 235000007340 Hordeum vulgare Nutrition 0.000 description 4
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 4
- 241000209504 Poaceae Species 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 4
- MGNCLNQXLYJVJD-UHFFFAOYSA-N cyanuric chloride Chemical compound ClC1=NC(Cl)=NC(Cl)=N1 MGNCLNQXLYJVJD-UHFFFAOYSA-N 0.000 description 4
- 230000035784 germination Effects 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- 239000002689 soil Substances 0.000 description 4
- 235000007319 Avena orientalis Nutrition 0.000 description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- 241000287127 Passeridae Species 0.000 description 3
- 244000062793 Sorghum vulgare Species 0.000 description 3
- 150000001412 amines Chemical class 0.000 description 3
- 239000003814 drug Substances 0.000 description 3
- 229940079593 drug Drugs 0.000 description 3
- 235000019713 millet Nutrition 0.000 description 3
- 238000006386 neutralization reaction Methods 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- 238000006467 substitution reaction Methods 0.000 description 3
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 2
- 235000005781 Avena Nutrition 0.000 description 2
- 240000002791 Brassica napus Species 0.000 description 2
- 235000004977 Brassica sinapistrum Nutrition 0.000 description 2
- BAVYZALUXZFZLV-UHFFFAOYSA-N Methylamine Chemical compound NC BAVYZALUXZFZLV-UHFFFAOYSA-N 0.000 description 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- 150000003973 alkyl amines Chemical class 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 239000005648 plant growth regulator Substances 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- -1 propylthio Chemical class 0.000 description 2
- YZHUMGUJCQRKBT-UHFFFAOYSA-M sodium chlorate Chemical compound [Na+].[O-]Cl(=O)=O YZHUMGUJCQRKBT-UHFFFAOYSA-M 0.000 description 2
- IROINLKCQGIITA-UHFFFAOYSA-N terbutryn Chemical compound CCNC1=NC(NC(C)(C)C)=NC(SC)=N1 IROINLKCQGIITA-UHFFFAOYSA-N 0.000 description 2
- JYEUMXHLPRZUAT-UHFFFAOYSA-N 1,2,3-triazine Chemical group C1=CN=NN=C1 JYEUMXHLPRZUAT-UHFFFAOYSA-N 0.000 description 1
- FBMDQVBGIYSDTI-UHFFFAOYSA-N 2-n,4-n-bis(3-methoxypropyl)-6-methylsulfanyl-1,3,5-triazine-2,4-diamine Chemical compound COCCCNC1=NC(NCCCOC)=NC(SC)=N1 FBMDQVBGIYSDTI-UHFFFAOYSA-N 0.000 description 1
- 241000254032 Acrididae Species 0.000 description 1
- 241000743985 Alopecurus Species 0.000 description 1
- 241000209764 Avena fatua Species 0.000 description 1
- 235000007558 Avena sp Nutrition 0.000 description 1
- 241000219310 Beta vulgaris subsp. vulgaris Species 0.000 description 1
- 244000024671 Brassica kaber Species 0.000 description 1
- 240000000385 Brassica napus var. napus Species 0.000 description 1
- GAWIXWVDTYZWAW-UHFFFAOYSA-N C[CH]O Chemical group C[CH]O GAWIXWVDTYZWAW-UHFFFAOYSA-N 0.000 description 1
- 241001483689 Camilla Species 0.000 description 1
- 244000025254 Cannabis sativa Species 0.000 description 1
- 241000207199 Citrus Species 0.000 description 1
- 240000007154 Coffea arabica Species 0.000 description 1
- 240000008067 Cucumis sativus Species 0.000 description 1
- 235000010799 Cucumis sativus var sativus Nutrition 0.000 description 1
- 235000002848 Cyperus flabelliformis Nutrition 0.000 description 1
- HCRWJJJUKUVORR-UHFFFAOYSA-N Desmetryn Chemical compound CNC1=NC(NC(C)C)=NC(SC)=N1 HCRWJJJUKUVORR-UHFFFAOYSA-N 0.000 description 1
- 240000001879 Digitalis lutea Species 0.000 description 1
- NPWMZOGDXOFZIN-UHFFFAOYSA-N Dipropetryn Chemical compound CCSC1=NC(NC(C)C)=NC(NC(C)C)=N1 NPWMZOGDXOFZIN-UHFFFAOYSA-N 0.000 description 1
- 244000058871 Echinochloa crus-galli Species 0.000 description 1
- 235000001950 Elaeis guineensis Nutrition 0.000 description 1
- 244000127993 Elaeis melanococca Species 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- 240000005702 Galium aparine Species 0.000 description 1
- 241000758791 Juglandaceae Species 0.000 description 1
- 241000520028 Lamium Species 0.000 description 1
- 235000007688 Lycopersicon esculentum Nutrition 0.000 description 1
- 244000042664 Matricaria chamomilla Species 0.000 description 1
- 240000005561 Musa balbisiana Species 0.000 description 1
- 240000004674 Papaver rhoeas Species 0.000 description 1
- 240000001090 Papaver somniferum Species 0.000 description 1
- 235000008753 Papaver somniferum Nutrition 0.000 description 1
- 244000104677 Peltiphyllum peltatum Species 0.000 description 1
- 235000014968 Peltiphyllum peltatum Nutrition 0.000 description 1
- 241000594009 Phoxinus phoxinus Species 0.000 description 1
- 241001130943 Phyllanthus <Aves> Species 0.000 description 1
- 231100000674 Phytotoxicity Toxicity 0.000 description 1
- 125000000066 S-methyl group Chemical group [H]C([H])([H])S* 0.000 description 1
- 240000000111 Saccharum officinarum Species 0.000 description 1
- 240000003768 Solanum lycopersicum Species 0.000 description 1
- 241000251778 Squalus acanthias Species 0.000 description 1
- 235000021536 Sugar beet Nutrition 0.000 description 1
- WFWLQNSHRPWKFK-UHFFFAOYSA-N Tegafur Chemical compound O=C1NC(=O)C(F)=CN1C1OCCC1 WFWLQNSHRPWKFK-UHFFFAOYSA-N 0.000 description 1
- 244000269722 Thea sinensis Species 0.000 description 1
- 244000299461 Theobroma cacao Species 0.000 description 1
- 235000009470 Theobroma cacao Nutrition 0.000 description 1
- 241000219094 Vitaceae Species 0.000 description 1
- 241000209149 Zea Species 0.000 description 1
- 240000008042 Zea mays Species 0.000 description 1
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 1
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 1
- RQVYBGPQFYCBGX-UHFFFAOYSA-N ametryn Chemical compound CCNC1=NC(NC(C)C)=NC(SC)=N1 RQVYBGPQFYCBGX-UHFFFAOYSA-N 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- MXWJVTOOROXGIU-UHFFFAOYSA-N atrazine Chemical compound CCNC1=NC(Cl)=NC(NC(C)C)=N1 MXWJVTOOROXGIU-UHFFFAOYSA-N 0.000 description 1
- 235000021015 bananas Nutrition 0.000 description 1
- 235000021028 berry Nutrition 0.000 description 1
- 125000001309 chloro group Chemical class Cl* 0.000 description 1
- 235000020971 citrus fruits Nutrition 0.000 description 1
- 235000016213 coffee Nutrition 0.000 description 1
- 235000013353 coffee beverage Nutrition 0.000 description 1
- 235000005822 corn Nutrition 0.000 description 1
- 125000000753 cycloalkyl group Chemical group 0.000 description 1
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 1
- 239000002837 defoliant Substances 0.000 description 1
- 239000002274 desiccant Substances 0.000 description 1
- 235000013399 edible fruits Nutrition 0.000 description 1
- 241001233957 eudicotyledons Species 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 235000021021 grapes Nutrition 0.000 description 1
- 235000021384 green leafy vegetables Nutrition 0.000 description 1
- 230000012010 growth Effects 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 125000000250 methylamino group Chemical group [H]N(*)C([H])([H])[H] 0.000 description 1
- QQSUFDHGUDRKPV-UHFFFAOYSA-N n-methylsulfanylcyclopentanamine Chemical class CSNC1CCCC1 QQSUFDHGUDRKPV-UHFFFAOYSA-N 0.000 description 1
- 235000012149 noodles Nutrition 0.000 description 1
- 239000002420 orchard Substances 0.000 description 1
- 239000012074 organic phase Substances 0.000 description 1
- 239000000575 pesticide Substances 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- AAEVYOVXGOFMJO-UHFFFAOYSA-N prometryn Chemical compound CSC1=NC(NC(C)C)=NC(NC(C)C)=N1 AAEVYOVXGOFMJO-UHFFFAOYSA-N 0.000 description 1
- 239000011814 protection agent Substances 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 239000012262 resinous product Substances 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011877 solvent mixture Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 235000013616 tea Nutrition 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 150000003918 triazines Chemical class 0.000 description 1
- RMLPZKRPSQVRAB-UHFFFAOYSA-N tris(3-methylphenyl) phosphate Chemical compound CC1=CC=CC(OP(=O)(OC=2C=C(C)C=CC=2)OC=2C=C(C)C=CC=2)=C1 RMLPZKRPSQVRAB-UHFFFAOYSA-N 0.000 description 1
- 235000020234 walnut Nutrition 0.000 description 1
- 238000009333 weeding Methods 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
- A01N43/64—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with three nitrogen atoms as the only ring hetero atoms
- A01N43/66—1,3,5-Triazines, not hydrogenated and not substituted at the ring nitrogen atoms
- A01N43/68—1,3,5-Triazines, not hydrogenated and not substituted at the ring nitrogen atoms with two or three nitrogen atoms directly attached to ring carbon atoms
- A01N43/70—Diamino—1,3,5—triazines with only one oxygen, sulfur or halogen atom or only one cyano, thiocyano (—SCN), cyanato (—OCN) or azido (—N3) group directly attached to a ring carbon atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D251/00—Heterocyclic compounds containing 1,3,5-triazine rings
- C07D251/02—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings
- C07D251/12—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
- C07D251/26—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with only hetero atoms directly attached to ring carbon atoms
- C07D251/40—Nitrogen atoms
- C07D251/42—One nitrogen atom
- C07D251/44—One nitrogen atom with halogen atoms attached to the two other ring carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D251/00—Heterocyclic compounds containing 1,3,5-triazine rings
- C07D251/02—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings
- C07D251/12—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
- C07D251/26—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with only hetero atoms directly attached to ring carbon atoms
- C07D251/40—Nitrogen atoms
- C07D251/48—Two nitrogen atoms
- C07D251/50—Two nitrogen atoms with a halogen atom attached to the third ring carbon atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D251/00—Heterocyclic compounds containing 1,3,5-triazine rings
- C07D251/02—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings
- C07D251/12—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
- C07D251/26—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with only hetero atoms directly attached to ring carbon atoms
- C07D251/40—Nitrogen atoms
- C07D251/48—Two nitrogen atoms
- C07D251/52—Two nitrogen atoms with an oxygen or sulfur atom attached to the third ring carbon atom
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- 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)
- Plural Heterocyclic Compounds (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19823222147 DE3222147A1 (de) | 1982-06-11 | 1982-06-11 | Verwendung gegebenenfalls substituierter thiomethylcycloalkylamino-s-triazine als selektive mittel gegen unkraeuter und schadgraeser |
| DE32221479 | 1982-06-11 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPS595103A true JPS595103A (ja) | 1984-01-12 |
Family
ID=6165922
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP58102984A Pending JPS595103A (ja) | 1982-06-11 | 1983-06-10 | 場合によつては置換されたチオメチル−シクロアルキルアミノ−ｓ−トリアジンを含有する選択的除草剤 |
Country Status (13)
| Country | Link |
|---|---|
| US (1) | US4615727A (enExample) |
| EP (1) | EP0096189A3 (enExample) |
| JP (1) | JPS595103A (enExample) |
| AU (1) | AU1494883A (enExample) |
| BR (1) | BR8303096A (enExample) |
| DE (1) | DE3222147A1 (enExample) |
| DK (1) | DK267483D0 (enExample) |
| FI (1) | FI832094A0 (enExample) |
| GR (1) | GR79306B (enExample) |
| MA (1) | MA19747A1 (enExample) |
| PL (1) | PL242465A1 (enExample) |
| SU (1) | SU1187701A3 (enExample) |
| ZA (1) | ZA834284B (enExample) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3420488A1 (de) * | 1984-06-01 | 1985-12-05 | Hüls AG, 4370 Marl | Verwendung von alkoxy-cycloalkylamino-s-triazinen zur selektiven behandlung von nutzpflanzen gegen unkraeuter und schadgraeser |
| DE4437137A1 (de) * | 1994-10-18 | 1996-04-25 | Hoechst Schering Agrevo Gmbh | Substituierte Cycloalkylamino- und -alkoxy-Heterocyclen, Verfahren zu ihrer Herstellung und ihre Verwendung als Schädlingsbekämpfungsmittel |
| AU2002216650A1 (en) | 2000-10-31 | 2002-05-15 | Lynn Bonham | Triazine derivatives as lpaat-b inhibitors and uses thereof |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CH492400A (de) * | 1968-03-20 | 1970-06-30 | Agripat Sa | Selektives Herbizid und dessen Verwendung zur Bekämpfung von Unkräutern und Ungräsern |
| GB1362366A (en) * | 1970-09-08 | 1974-08-07 | Degussa | Propion-amidotriazines and agent for regulating plant growth |
| US3714162A (en) * | 1971-03-24 | 1973-01-30 | Monsanto Co | New herbicidal n-(1-cycloalken-1-yl)-amino-s-triazine compounds |
| US3766182A (en) * | 1971-05-26 | 1973-10-16 | Ciba Geigy Corp | S-triazine derivatives |
| US3786053A (en) * | 1971-09-07 | 1974-01-15 | Degussa | Propionamido triazine |
| CH588213A5 (enExample) * | 1974-07-25 | 1977-05-31 | Ciba Geigy Ag | |
| CS197620B1 (en) * | 1977-08-01 | 1980-05-30 | Jan Kralovic | Agent for enhancement of root yield and sugar content of sugar beet |
-
1982
- 1982-06-11 DE DE19823222147 patent/DE3222147A1/de not_active Withdrawn
-
1983
- 1983-03-18 MA MA19965A patent/MA19747A1/fr unknown
- 1983-04-14 EP EP83103610A patent/EP0096189A3/de not_active Ceased
- 1983-05-25 AU AU14948/83A patent/AU1494883A/en not_active Abandoned
- 1983-06-02 US US06/500,381 patent/US4615727A/en not_active Expired - Fee Related
- 1983-06-09 SU SU833600942A patent/SU1187701A3/ru active
- 1983-06-10 BR BR8303096A patent/BR8303096A/pt unknown
- 1983-06-10 JP JP58102984A patent/JPS595103A/ja active Pending
- 1983-06-10 FI FI832094A patent/FI832094A0/fi not_active Application Discontinuation
- 1983-06-10 PL PL24246583A patent/PL242465A1/xx unknown
- 1983-06-10 ZA ZA834284A patent/ZA834284B/xx unknown
- 1983-06-10 DK DK2674/83A patent/DK267483D0/da not_active Application Discontinuation
- 1983-06-22 GR GR71571A patent/GR79306B/el unknown
Also Published As
| Publication number | Publication date |
|---|---|
| MA19747A1 (fr) | 1983-10-01 |
| EP0096189A2 (de) | 1983-12-21 |
| US4615727A (en) | 1986-10-07 |
| DE3222147A1 (de) | 1983-12-15 |
| AU1494883A (en) | 1983-12-15 |
| GR79306B (enExample) | 1984-10-22 |
| BR8303096A (pt) | 1984-01-31 |
| FI832094A0 (fi) | 1983-06-10 |
| ZA834284B (en) | 1984-03-28 |
| SU1187701A3 (ru) | 1985-10-23 |
| DK267483D0 (da) | 1983-06-10 |
| EP0096189A3 (de) | 1984-12-27 |
| PL242465A1 (en) | 1984-07-16 |
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