CS227043B2 - Herbicide and plant growth regulating composition,and method of preparing active substances thereof - Google Patents
Herbicide and plant growth regulating composition,and method of preparing active substances thereof Download PDFInfo
- Publication number
- CS227043B2 CS227043B2 CS821972A CS197282A CS227043B2 CS 227043 B2 CS227043 B2 CS 227043B2 CS 821972 A CS821972 A CS 821972A CS 197282 A CS197282 A CS 197282A CS 227043 B2 CS227043 B2 CS 227043B2
- Authority
- CS
- Czechoslovakia
- Prior art keywords
- formula
- compounds
- urea
- alkyl
- growth
- Prior art date
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- 239000000203 mixture Substances 0.000 title claims description 23
- 230000002363 herbicidal effect Effects 0.000 title claims description 18
- 238000000034 method Methods 0.000 title claims description 13
- 230000008635 plant growth Effects 0.000 title claims description 8
- 230000001105 regulatory effect Effects 0.000 title claims description 4
- 239000004009 herbicide Substances 0.000 title description 6
- 239000013543 active substance Substances 0.000 title description 4
- 239000000460 chlorine Substances 0.000 claims description 99
- 150000001875 compounds Chemical class 0.000 claims description 59
- 239000004480 active ingredient Substances 0.000 claims description 17
- 238000002360 preparation method Methods 0.000 claims description 12
- 150000003839 salts Chemical class 0.000 claims description 10
- 125000000217 alkyl group Chemical group 0.000 claims description 8
- 238000006243 chemical reaction Methods 0.000 claims description 7
- 229910052736 halogen Inorganic materials 0.000 claims description 7
- 150000002367 halogens Chemical class 0.000 claims description 7
- 229910052739 hydrogen Inorganic materials 0.000 claims description 7
- 239000001257 hydrogen Substances 0.000 claims description 6
- 229910000039 hydrogen halide Inorganic materials 0.000 claims description 6
- 239000012433 hydrogen halide Substances 0.000 claims description 6
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 4
- 230000029936 alkylation Effects 0.000 claims description 4
- 238000005804 alkylation reaction Methods 0.000 claims description 4
- 230000015572 biosynthetic process Effects 0.000 claims description 4
- 238000003776 cleavage reaction Methods 0.000 claims description 4
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- 125000004306 triazinyl group Chemical group 0.000 claims description 4
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 3
- 125000003545 alkoxy group Chemical group 0.000 claims description 3
- 229910052801 chlorine Inorganic materials 0.000 claims description 3
- XTFIVUDBNACUBN-UHFFFAOYSA-N 1,3,5-trinitro-1,3,5-triazinane Chemical compound [O-][N+](=O)N1CN([N+]([O-])=O)CN([N+]([O-])=O)C1 XTFIVUDBNACUBN-UHFFFAOYSA-N 0.000 claims description 2
- 125000006374 C2-C10 alkenyl group Chemical group 0.000 claims description 2
- 150000002431 hydrogen Chemical class 0.000 claims description 2
- 125000001188 haloalkyl group Chemical group 0.000 claims 1
- -1 N- (4-chloro-6-isopropylamino-1,3,5-triazin-2-yl) -N-isopropyl-N '- (4-chlorophenylsulfonyl) urea Chemical compound 0.000 description 41
- 241000196324 Embryophyta Species 0.000 description 40
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- 238000002844 melting Methods 0.000 description 18
- 230000008018 melting Effects 0.000 description 18
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- 101150065749 Churc1 gene Proteins 0.000 description 13
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- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 10
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- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 8
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- HEMHJVSKTPXQMS-UHFFFAOYSA-M sodium hydroxide Inorganic materials [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 5
- 239000002904 solvent Substances 0.000 description 5
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- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
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- 231100000001 growth retardation Toxicity 0.000 description 3
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- 235000002637 Nicotiana tabacum Nutrition 0.000 description 1
- 244000061176 Nicotiana tabacum Species 0.000 description 1
- IGFHQQFPSIBGKE-UHFFFAOYSA-N Nonylphenol Natural products CCCCCCCCCC1=CC=C(O)C=C1 IGFHQQFPSIBGKE-UHFFFAOYSA-N 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 235000010627 Phaseolus vulgaris Nutrition 0.000 description 1
- 244000046052 Phaseolus vulgaris Species 0.000 description 1
- YGYAWVDWMABLBF-UHFFFAOYSA-N Phosgene Chemical compound ClC(Cl)=O YGYAWVDWMABLBF-UHFFFAOYSA-N 0.000 description 1
- 241000209504 Poaceae Species 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
- 229920001214 Polysorbate 60 Polymers 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- 239000006004 Quartz sand Substances 0.000 description 1
- 235000007201 Saccharum officinarum Nutrition 0.000 description 1
- 241000220261 Sinapis Species 0.000 description 1
- KEAYESYHFKHZAL-UHFFFAOYSA-N Sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 1
- 229920002125 Sokalan® Polymers 0.000 description 1
- 229930006000 Sucrose Natural products 0.000 description 1
- CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 description 1
- 235000021536 Sugar beet 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
- 230000000274 adsorptive effect Effects 0.000 description 1
- 230000001476 alcoholic effect Effects 0.000 description 1
- 125000004453 alkoxycarbonyl group Chemical group 0.000 description 1
- 125000002877 alkyl aryl group Chemical group 0.000 description 1
- 125000004414 alkyl thio group Chemical group 0.000 description 1
- 239000002168 alkylating agent Substances 0.000 description 1
- 229940100198 alkylating agent Drugs 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 239000007900 aqueous suspension Substances 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 229960000892 attapulgite Drugs 0.000 description 1
- 150000007514 bases Chemical class 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
- 239000011230 binding agent Substances 0.000 description 1
- 230000004071 biological effect Effects 0.000 description 1
- 230000033228 biological regulation Effects 0.000 description 1
- 230000031709 bromination Effects 0.000 description 1
- 238000005893 bromination reaction Methods 0.000 description 1
- 229910052794 bromium Inorganic materials 0.000 description 1
- RDHPKYGYEGBMSE-UHFFFAOYSA-N bromoethane Chemical compound CCBr RDHPKYGYEGBMSE-UHFFFAOYSA-N 0.000 description 1
- 159000000007 calcium salts Chemical class 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 150000001768 cations Chemical class 0.000 description 1
- 238000005660 chlorination reaction Methods 0.000 description 1
- NEHMKBQYUWJMIP-UHFFFAOYSA-N chloromethane Chemical compound ClC NEHMKBQYUWJMIP-UHFFFAOYSA-N 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- MGNCLNQXLYJVJD-UHFFFAOYSA-N cyanuric chloride Chemical compound ClC1=NC(Cl)=NC(Cl)=N1 MGNCLNQXLYJVJD-UHFFFAOYSA-N 0.000 description 1
- 238000001212 derivatisation Methods 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 229940060296 dodecylbenzenesulfonic acid Drugs 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 239000002024 ethyl acetate extract Substances 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 230000001605 fetal effect Effects 0.000 description 1
- 210000003754 fetus Anatomy 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000000417 fungicide Substances 0.000 description 1
- 230000035784 germination Effects 0.000 description 1
- 238000005469 granulation Methods 0.000 description 1
- 230000003179 granulation Effects 0.000 description 1
- 150000002357 guanidines Chemical class 0.000 description 1
- 229940083094 guanine derivative acting on arteriolar smooth muscle Drugs 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 239000003701 inert diluent Substances 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 150000007529 inorganic bases Chemical class 0.000 description 1
- 239000002917 insecticide Substances 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- INQOMBQAUSQDDS-UHFFFAOYSA-N iodomethane Chemical compound IC INQOMBQAUSQDDS-UHFFFAOYSA-N 0.000 description 1
- 239000012948 isocyanate Substances 0.000 description 1
- 150000002513 isocyanates Chemical class 0.000 description 1
- 150000002540 isothiocyanates Chemical class 0.000 description 1
- 229910052622 kaolinite Inorganic materials 0.000 description 1
- 229920005610 lignin Polymers 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 230000014759 maintenance of location Effects 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
- 239000002480 mineral oil Substances 0.000 description 1
- ZRVCTYCTIIJARH-UHFFFAOYSA-N n-sulfonylcarbamoyl chloride Chemical class ClC(=O)N=S(=O)=O ZRVCTYCTIIJARH-UHFFFAOYSA-N 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 230000020477 pH reduction Effects 0.000 description 1
- 229910052625 palygorskite Inorganic materials 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 230000008654 plant damage Effects 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 239000004584 polyacrylic acid Substances 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 description 1
- 159000000001 potassium salts Chemical class 0.000 description 1
- 230000003389 potentiating effect Effects 0.000 description 1
- OSFBJERFMQCEQY-UHFFFAOYSA-N propylidene Chemical compound [CH]CC OSFBJERFMQCEQY-UHFFFAOYSA-N 0.000 description 1
- 239000008262 pumice Substances 0.000 description 1
- 229910052903 pyrophyllite Inorganic materials 0.000 description 1
- 239000010453 quartz Substances 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 230000000979 retarding effect Effects 0.000 description 1
- 238000007363 ring formation reaction Methods 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000012312 sodium hydride Substances 0.000 description 1
- 229910000104 sodium hydride Inorganic materials 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000004575 stone Substances 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 239000005720 sucrose Substances 0.000 description 1
- 229940124530 sulfonamide Drugs 0.000 description 1
- 239000013589 supplement Substances 0.000 description 1
- 230000001629 suppression Effects 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- ZWZVWGITAAIFPS-UHFFFAOYSA-N thiophosgene Chemical compound ClC(Cl)=S ZWZVWGITAAIFPS-UHFFFAOYSA-N 0.000 description 1
- 150000003672 ureas Chemical class 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C303/00—Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides
- C07C303/36—Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides of amides of sulfonic acids
- C07C303/40—Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides of amides of sulfonic acids by reactions not involving the formation of sulfonamide groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D521/00—Heterocyclic compounds containing unspecified hetero rings
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
- A01N47/28—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N<
- A01N47/36—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N< containing the group >N—CO—N< directly attached to at least one heterocyclic ring; Thio analogues thereof
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- Plant Pathology (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Plural Heterocyclic Compounds (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE3111451A DE3111451A1 (de) | 1981-03-24 | 1981-03-24 | "heterocyclisch substituierte (halogen)alkyl- und alkoxysulfonylharnstoffe, verfahren zu ihrer herstellung und ihre verwendung in der landwirtschaft" |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CS227043B2 true CS227043B2 (en) | 1984-04-16 |
Family
ID=6128104
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CS821972A CS227043B2 (en) | 1981-03-24 | 1982-03-22 | Herbicide and plant growth regulating composition,and method of preparing active substances thereof |
Country Status (17)
| Country | Link |
|---|---|
| US (1) | US4440565A (fr) |
| EP (1) | EP0061661A1 (fr) |
| JP (1) | JPS57169469A (fr) |
| KR (1) | KR830009053A (fr) |
| AU (1) | AU551443B2 (fr) |
| BR (1) | BR8201601A (fr) |
| CA (1) | CA1230337A (fr) |
| CS (1) | CS227043B2 (fr) |
| DD (1) | DD202378A5 (fr) |
| DE (1) | DE3111451A1 (fr) |
| DK (1) | DK131682A (fr) |
| ES (2) | ES8403464A1 (fr) |
| IL (1) | IL65314A (fr) |
| NZ (1) | NZ200087A (fr) |
| PT (1) | PT74625B (fr) |
| ZA (1) | ZA821956B (fr) |
| ZW (1) | ZW5582A1 (fr) |
Families Citing this family (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4474601A (en) * | 1980-07-11 | 1984-10-02 | E. I. Du Pont De Nemours And Company | Herbicidal alkenyl benzenesulfonamide |
| DE3111451A1 (de) * | 1981-03-24 | 1982-10-07 | Hoechst Ag, 6000 Frankfurt | "heterocyclisch substituierte (halogen)alkyl- und alkoxysulfonylharnstoffe, verfahren zu ihrer herstellung und ihre verwendung in der landwirtschaft" |
| DE3131489A1 (de) * | 1981-08-08 | 1983-02-24 | Hoechst Ag, 6000 Frankfurt | Heterocyclisch substituierte sulfonylharnstoffe, verfahren zu ihrer herstellung und ihre verwendung in der landwirtschaft |
| AU571869B2 (en) * | 1983-05-09 | 1988-04-28 | E.I. Du Pont De Nemours And Company | Pyridyl- and pyrimidyl- sulphonamides |
| DE3324802A1 (de) * | 1983-07-09 | 1985-01-17 | Hoechst Ag, 6230 Frankfurt | Neue n-alkoxy- und n- alkylsulfonylaminosulfonylharnstoffe, und neue (pyrimido) triazino-thiadiazinoxide als vorprodukte |
| US4588432A (en) * | 1984-02-27 | 1986-05-13 | E. I. Du Pont De Nemours And Company | Herbicidal selenylsulfonamides |
| DE3811777A1 (de) * | 1988-04-08 | 1989-10-19 | Hoechst Ag | Heterocyclisch substituierte alkyl- und alkenylsulfonylharnstoffe, verfahren zu ihrer herstellung und ihre verwendung als herbizide oder pflanzenwachstumsregulatoren |
| DE3826609A1 (de) * | 1988-08-05 | 1990-02-08 | Hoechst Ag | Heterocyclisch substituierte sulfonylharnstoffe, verfahren zu ihrer herstellung und ihre verwendung als herbizide oder pflanzenwachstumsregulatoren |
| ATE113938T1 (de) * | 1989-07-19 | 1994-11-15 | Hoechst Schering Agrevo Gmbh | Heterocyclisch substituierte sulfonylharnstoffe, verfahren zu ihrer herstellung und ihre verwendung als herbizide oder pflanzenwachstumsregulatoren. |
| DE4021489A1 (de) * | 1990-07-06 | 1992-01-09 | Hoechst Ag | Substituierte sulfonalkylsulfonylharnstoffe, verfahren zu ihrer herstellung und ihre verwendung als herbizide und pflanzenwachstumsregulatoren |
| JP3355237B2 (ja) * | 1993-10-15 | 2002-12-09 | 呉羽化学工業株式会社 | N−(置換アミノ)ピロール誘導体、その製造方法及び除草剤 |
| JPH0827147A (ja) | 1994-07-20 | 1996-01-30 | Kureha Chem Ind Co Ltd | N−(置換アミノ)イミド誘導体、その製造方法及び除草剤 |
| US20060025468A1 (en) * | 2004-07-29 | 2006-02-02 | Whitten Jeffrey P | Chiral pyrrolidine derivatives, and methods for preparing compounds thereof |
| EP3668840A1 (fr) | 2017-08-15 | 2020-06-24 | Inflazome Limited | Nouveaux composés de sulfonamide carboxamide |
| WO2019043610A1 (fr) * | 2017-08-31 | 2019-03-07 | Cadila Healthcare Limited | Nouveaux dérivés de sulfonylurées substitués |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA1082189A (fr) * | 1976-04-07 | 1980-07-22 | George Levitt | Sulfamides herbicides |
| US4191553A (en) * | 1978-03-02 | 1980-03-04 | E. I. Du Pont De Nemours And Company | Herbicidal sulfamates |
| US4238621A (en) * | 1979-04-13 | 1980-12-09 | E. I. Du Pont De Nemours And Company | Intermediates for herbicidal sulfonamides |
| CA1221687A (fr) * | 1980-11-03 | 1987-05-12 | Richard F. Sauers | Sulfonamides herbicides |
| DE3111451A1 (de) * | 1981-03-24 | 1982-10-07 | Hoechst Ag, 6000 Frankfurt | "heterocyclisch substituierte (halogen)alkyl- und alkoxysulfonylharnstoffe, verfahren zu ihrer herstellung und ihre verwendung in der landwirtschaft" |
-
1981
- 1981-03-24 DE DE3111451A patent/DE3111451A1/de not_active Withdrawn
-
1982
- 1982-03-16 ES ES510475A patent/ES8403464A1/es not_active Expired
- 1982-03-18 EP EP82102200A patent/EP0061661A1/fr not_active Withdrawn
- 1982-03-22 NZ NZ200087A patent/NZ200087A/en unknown
- 1982-03-22 KR KR1019820001203A patent/KR830009053A/ko not_active Withdrawn
- 1982-03-22 ZW ZW55/82A patent/ZW5582A1/xx unknown
- 1982-03-22 DD DD82238348A patent/DD202378A5/de unknown
- 1982-03-22 US US06/360,489 patent/US4440565A/en not_active Expired - Fee Related
- 1982-03-22 PT PT74625A patent/PT74625B/pt unknown
- 1982-03-22 IL IL65314A patent/IL65314A/xx unknown
- 1982-03-22 CS CS821972A patent/CS227043B2/cs unknown
- 1982-03-23 BR BR8201601A patent/BR8201601A/pt unknown
- 1982-03-23 CA CA000399187A patent/CA1230337A/fr not_active Expired
- 1982-03-23 AU AU81820/82A patent/AU551443B2/en not_active Ceased
- 1982-03-23 ZA ZA821956A patent/ZA821956B/xx unknown
- 1982-03-23 JP JP57044756A patent/JPS57169469A/ja active Pending
- 1982-03-23 DK DK131682A patent/DK131682A/da not_active IP Right Cessation
-
1983
- 1983-03-15 ES ES520621A patent/ES520621A0/es active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| DD202378A5 (de) | 1983-09-14 |
| JPS57169469A (en) | 1982-10-19 |
| PT74625A (en) | 1982-04-01 |
| BR8201601A (pt) | 1983-02-08 |
| US4440565A (en) | 1984-04-03 |
| ES510475A0 (es) | 1983-06-01 |
| AU8182082A (en) | 1982-09-30 |
| ES8403464A1 (es) | 1983-06-01 |
| ZA821956B (en) | 1983-02-23 |
| ES8402696A1 (es) | 1984-03-16 |
| KR830009053A (ko) | 1983-12-17 |
| IL65314A (en) | 1985-12-31 |
| NZ200087A (en) | 1985-04-30 |
| EP0061661A1 (fr) | 1982-10-06 |
| AU551443B2 (en) | 1986-05-01 |
| DE3111451A1 (de) | 1982-10-07 |
| ZW5582A1 (en) | 1982-10-20 |
| CA1230337A (fr) | 1987-12-15 |
| PT74625B (en) | 1984-01-04 |
| IL65314A0 (en) | 1982-05-31 |
| ES520621A0 (es) | 1984-03-16 |
| DK131682A (da) | 1982-09-25 |
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