SE450638B - Guaniderade aminofosfonsyraforeningar, forfarande for framstellning av dessa och anvendning av foreningarna som biocider - Google Patents
Guaniderade aminofosfonsyraforeningar, forfarande for framstellning av dessa och anvendning av foreningarna som biociderInfo
- Publication number
- SE450638B SE450638B SE8303499A SE8303499A SE450638B SE 450638 B SE450638 B SE 450638B SE 8303499 A SE8303499 A SE 8303499A SE 8303499 A SE8303499 A SE 8303499A SE 450638 B SE450638 B SE 450638B
- Authority
- SE
- Sweden
- Prior art keywords
- acid
- guanidated
- compounds
- water
- mmol
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 title claims description 47
- 238000000034 method Methods 0.000 title claims description 8
- 239000003139 biocide Substances 0.000 title claims description 3
- 239000000126 substance Substances 0.000 title description 15
- PTMHPRAIXMAOOB-UHFFFAOYSA-N phosphoramidic acid Chemical compound NP(O)(O)=O PTMHPRAIXMAOOB-UHFFFAOYSA-N 0.000 title description 5
- 239000002253 acid Substances 0.000 claims description 30
- 238000002360 preparation method Methods 0.000 claims description 21
- 150000003839 salts Chemical class 0.000 claims description 14
- 239000003153 chemical reaction reagent Substances 0.000 claims description 12
- 238000006243 chemical reaction Methods 0.000 claims description 11
- 229910052739 hydrogen Inorganic materials 0.000 claims description 10
- 239000001257 hydrogen Substances 0.000 claims description 10
- 150000001412 amines Chemical class 0.000 claims description 8
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 6
- XZMCDFZZKTWFGF-UHFFFAOYSA-N Cyanamide Chemical compound NC#N XZMCDFZZKTWFGF-UHFFFAOYSA-N 0.000 claims description 5
- 229910052783 alkali metal Inorganic materials 0.000 claims description 5
- 150000001340 alkali metals Chemical class 0.000 claims description 5
- 125000004103 aminoalkyl group Chemical group 0.000 claims description 4
- UEZVMMHDMIWARA-UHFFFAOYSA-M phosphonate Chemical compound [O-]P(=O)=O UEZVMMHDMIWARA-UHFFFAOYSA-M 0.000 claims description 4
- 239000007864 aqueous solution Substances 0.000 claims description 2
- 229910052736 halogen Inorganic materials 0.000 claims description 2
- 150000004985 diamines Chemical group 0.000 claims 1
- 125000005843 halogen group Chemical group 0.000 claims 1
- RMAHPRNLQIRHIJ-UHFFFAOYSA-N methyl carbamimidate Chemical compound COC(N)=N RMAHPRNLQIRHIJ-UHFFFAOYSA-N 0.000 claims 1
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 42
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 39
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 20
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 20
- 239000000243 solution Substances 0.000 description 16
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 14
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 12
- 230000008018 melting Effects 0.000 description 12
- 238000002844 melting Methods 0.000 description 12
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 9
- -1 isothiouronium compound Chemical class 0.000 description 9
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 8
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 8
- 238000001953 recrystallisation Methods 0.000 description 8
- 125000002947 alkylene group Chemical group 0.000 description 7
- 239000007787 solid Substances 0.000 description 7
- KRYWEAYKLGCRRH-UHFFFAOYSA-N [amino(methylsulfanyl)methylidene]azanium;chloride Chemical compound Cl.CSC(N)=N KRYWEAYKLGCRRH-UHFFFAOYSA-N 0.000 description 6
- MOFCYHDQWIZKMY-UHFFFAOYSA-N chloromethylphosphonic acid Chemical compound OP(O)(=O)CCl MOFCYHDQWIZKMY-UHFFFAOYSA-N 0.000 description 6
- 239000000706 filtrate Substances 0.000 description 6
- ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical compound OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 description 5
- 239000000417 fungicide Substances 0.000 description 5
- 239000000543 intermediate Substances 0.000 description 5
- WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical compound [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 description 4
- 125000004432 carbon atom Chemical group C* 0.000 description 4
- 238000001035 drying Methods 0.000 description 4
- 150000002431 hydrogen Chemical group 0.000 description 4
- 150000007524 organic acids Chemical class 0.000 description 4
- 235000005985 organic acids Nutrition 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- 239000011780 sodium chloride Substances 0.000 description 4
- LPKCJFLRJWWIDI-UHFFFAOYSA-N (diaminomethylideneamino)phosphonic acid Chemical compound NC(N)=NP(O)(O)=O LPKCJFLRJWWIDI-UHFFFAOYSA-N 0.000 description 3
- 229920001817 Agar Polymers 0.000 description 3
- 239000008272 agar Substances 0.000 description 3
- 239000013078 crystal Substances 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 229920000768 polyamine Polymers 0.000 description 3
- 239000002244 precipitate Substances 0.000 description 3
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 3
- 125000000467 secondary amino group Chemical group [H]N([*:1])[*:2] 0.000 description 3
- 239000007858 starting material Substances 0.000 description 3
- 150000003672 ureas Chemical class 0.000 description 3
- PWGJDPKCLMLPJW-UHFFFAOYSA-N 1,8-diaminooctane Chemical compound NCCCCCCCCN PWGJDPKCLMLPJW-UHFFFAOYSA-N 0.000 description 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 2
- 241000233866 Fungi Species 0.000 description 2
- 241000736122 Parastagonospora nodorum Species 0.000 description 2
- 241000228453 Pyrenophora Species 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- 125000003368 amide group Chemical group 0.000 description 2
- 125000003277 amino group Chemical group 0.000 description 2
- 230000003115 biocidal effect Effects 0.000 description 2
- 239000007795 chemical reaction product Substances 0.000 description 2
- 239000000460 chlorine Substances 0.000 description 2
- 229910052801 chlorine Inorganic materials 0.000 description 2
- KCIDZIIHRGYJAE-YGFYJFDDSA-L dipotassium;[(2r,3r,4s,5r,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] phosphate Chemical class [K+].[K+].OC[C@H]1O[C@H](OP([O-])([O-])=O)[C@H](O)[C@@H](O)[C@H]1O KCIDZIIHRGYJAE-YGFYJFDDSA-L 0.000 description 2
- 235000021186 dishes Nutrition 0.000 description 2
- 238000010265 fast atom bombardment Methods 0.000 description 2
- 230000000855 fungicidal effect Effects 0.000 description 2
- 238000003898 horticulture Methods 0.000 description 2
- 239000002917 insecticide Substances 0.000 description 2
- 150000004682 monohydrates Chemical class 0.000 description 2
- 239000001103 potassium chloride Substances 0.000 description 2
- 235000011164 potassium chloride Nutrition 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- NDPOKRAFNXXKFB-UHFFFAOYSA-N (10-aminodecylamino)methylphosphonic acid;hydrate Chemical compound O.NCCCCCCCCCCNCP(O)(O)=O NDPOKRAFNXXKFB-UHFFFAOYSA-N 0.000 description 1
- BDHLENCBZHPMAH-UHFFFAOYSA-N (6-aminohexylamino)methylphosphonic acid;hydrate Chemical compound O.NCCCCCCNCP(O)(O)=O BDHLENCBZHPMAH-UHFFFAOYSA-N 0.000 description 1
- MGRVRXRGTBOSHW-UHFFFAOYSA-N (aminomethyl)phosphonic acid Chemical compound NCP(O)(O)=O MGRVRXRGTBOSHW-UHFFFAOYSA-N 0.000 description 1
- MCFBUIIRFZBRCU-UHFFFAOYSA-N 4-[1-[5-[6-(trifluoromethyl)-1h-benzimidazol-2-yl]pyridin-2-yl]piperidin-4-yl]oxycyclohexane-1-carboxylic acid Chemical compound C1CC(C(=O)O)CCC1OC1CCN(C=2N=CC(=CC=2)C=2NC3=CC(=CC=C3N=2)C(F)(F)F)CC1 MCFBUIIRFZBRCU-UHFFFAOYSA-N 0.000 description 1
- 241001465180 Botrytis Species 0.000 description 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- 241000122692 Fusarium avenaceum Species 0.000 description 1
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 1
- 241001330975 Magnaporthe oryzae Species 0.000 description 1
- 241000813090 Rhizoctonia solani Species 0.000 description 1
- 235000002595 Solanum tuberosum Nutrition 0.000 description 1
- 244000061456 Solanum tuberosum Species 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
- OYRCQPLOFVAQGC-UHFFFAOYSA-N [10-(diaminomethylideneamino)decylamino]methylphosphonic acid Chemical compound NC(N)=NCCCCCCCCCCNCP(O)(O)=O OYRCQPLOFVAQGC-UHFFFAOYSA-N 0.000 description 1
- 150000001242 acetic acid derivatives Chemical class 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 230000000844 anti-bacterial effect Effects 0.000 description 1
- 239000004599 antimicrobial Substances 0.000 description 1
- 239000003899 bactericide agent Substances 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
- 229910052794 bromium Inorganic materials 0.000 description 1
- QVYARBLCAHCSFJ-UHFFFAOYSA-N butane-1,1-diamine Chemical compound CCCC(N)N QVYARBLCAHCSFJ-UHFFFAOYSA-N 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 239000002738 chelating agent Substances 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 239000008121 dextrose Substances 0.000 description 1
- 125000004177 diethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 201000010099 disease Diseases 0.000 description 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- OQGSHLFKXYVLRR-UHFFFAOYSA-N dodecane-1,2-diamine Chemical compound CCCCCCCCCCC(N)CN OQGSHLFKXYVLRR-UHFFFAOYSA-N 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 244000000004 fungal plant pathogen Species 0.000 description 1
- 150000002367 halogens Chemical group 0.000 description 1
- 239000004009 herbicide Substances 0.000 description 1
- NAQMVNRVTILPCV-UHFFFAOYSA-N hexane-1,6-diamine Chemical compound NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 description 1
- 238000011534 incubation Methods 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 238000004949 mass spectrometry Methods 0.000 description 1
- 238000001819 mass spectrum Methods 0.000 description 1
- 235000010755 mineral Nutrition 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 230000017066 negative regulation of growth Effects 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 230000003472 neutralizing effect Effects 0.000 description 1
- SXJVFQLYZSNZBT-UHFFFAOYSA-N nonane-1,9-diamine Chemical compound NCCCCCCCCCN SXJVFQLYZSNZBT-UHFFFAOYSA-N 0.000 description 1
- 229940049964 oleate Drugs 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- 239000012071 phase Substances 0.000 description 1
- 150000003009 phosphonic acids Chemical class 0.000 description 1
- 235000012015 potatoes Nutrition 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 239000007790 solid phase Substances 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/28—Phosphorus compounds with one or more P—C bonds
- C07F9/38—Phosphonic acids [RP(=O)(OH)2]; Thiophosphonic acids ; [RP(=X1)(X2H)2(X1, X2 are each independently O, S or Se)]
- C07F9/3804—Phosphonic acids [RP(=O)(OH)2]; Thiophosphonic acids ; [RP(=X1)(X2H)2(X1, X2 are each independently O, S or Se)] not used, see subgroups
- C07F9/3808—Acyclic saturated acids which can have further substituents on alkyl
-
- 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
- A01N57/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds
- A01N57/18—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-carbon bonds
- A01N57/20—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-carbon bonds containing acyclic or cycloaliphatic radicals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/28—Phosphorus compounds with one or more P—C bonds
- C07F9/38—Phosphonic acids [RP(=O)(OH)2]; Thiophosphonic acids ; [RP(=X1)(X2H)2(X1, X2 are each independently O, S or Se)]
- C07F9/40—Esters thereof
- C07F9/4003—Esters thereof the acid moiety containing a substituent or a structure which is considered as characteristic
- C07F9/4006—Esters of acyclic acids which can have further substituents on alkyl
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Biochemistry (AREA)
- Molecular Biology (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (AREA)
- Plant Pathology (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Priority Applications (11)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| SE8303499A SE450638B (sv) | 1983-06-17 | 1983-06-17 | Guaniderade aminofosfonsyraforeningar, forfarande for framstellning av dessa och anvendning av foreningarna som biocider |
| AT84902546T ATE29502T1 (de) | 1983-06-17 | 1984-06-15 | Guanidierte aminophosphonsaeure-verbindungen. |
| JP59502533A JPS60501606A (ja) | 1983-06-17 | 1984-06-15 | グアニジン化アミノホスホン酸化合物、それらの製造法及び殺生物剤 |
| ES533465A ES533465A0 (es) | 1983-06-17 | 1984-06-15 | Un procedimiento para preparar derivados de acidos n-(aminoalquil)-aminoalcanfosfonicos guanidados |
| AU30688/84A AU3068884A (en) | 1983-06-17 | 1984-06-15 | Guanidated aminophosphonic acid compounds |
| EP84902546A EP0144420B1 (en) | 1983-06-17 | 1984-06-15 | Guanidated aminophosphonic acid compounds |
| IT48407/84A IT1177801B (it) | 1983-06-17 | 1984-06-15 | Derivati di acidi amminofosfonici guamidati dotati di attivita' biocida e loro procedimento di preparazione |
| PCT/SE1984/000224 WO1985000038A1 (en) | 1983-06-17 | 1984-06-15 | Guanidated aminophosphonic acid compounds |
| US06/705,342 US4600429A (en) | 1983-06-17 | 1984-06-15 | Guanidated aminophosphonic acid compounds |
| DE8484902546T DE3465999D1 (en) | 1983-06-17 | 1984-06-15 | Guanidated aminophosphonic acid compounds |
| FI850555A FI75576C (fi) | 1983-06-17 | 1985-02-11 | Guaniderade aminofosfonsyrafoereningar, deras framstaellning och anvaendning samt i foerfarandet anvaendbara mellanprodukter. |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| SE8303499A SE450638B (sv) | 1983-06-17 | 1983-06-17 | Guaniderade aminofosfonsyraforeningar, forfarande for framstellning av dessa och anvendning av foreningarna som biocider |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| SE8303499D0 SE8303499D0 (sv) | 1983-06-17 |
| SE8303499L SE8303499L (sv) | 1984-12-18 |
| SE450638B true SE450638B (sv) | 1987-07-13 |
Family
ID=20351669
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SE8303499A SE450638B (sv) | 1983-06-17 | 1983-06-17 | Guaniderade aminofosfonsyraforeningar, forfarande for framstellning av dessa och anvendning av foreningarna som biocider |
Country Status (10)
| Country | Link |
|---|---|
| US (1) | US4600429A (fi) |
| EP (1) | EP0144420B1 (fi) |
| JP (1) | JPS60501606A (fi) |
| AU (1) | AU3068884A (fi) |
| DE (1) | DE3465999D1 (fi) |
| ES (1) | ES533465A0 (fi) |
| FI (1) | FI75576C (fi) |
| IT (1) | IT1177801B (fi) |
| SE (1) | SE450638B (fi) |
| WO (1) | WO1985000038A1 (fi) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7491725B2 (en) | 2004-02-06 | 2009-02-17 | Bristol-Myers Squibb Company | Process for preparing 2-aminothiazole-5-aromatic carboxamides as kinase inhibitors |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2599807A (en) * | 1950-06-01 | 1952-06-10 | Frederick C Bersworth | Alkylene polyamine methylene phosphonic acids |
| US3322863A (en) * | 1963-09-09 | 1967-05-30 | Dow Chemical Co | Aminoalkyl phosphonates and preparation thereof |
| US3470112A (en) * | 1966-03-29 | 1969-09-30 | Monsanto Co | Polymeric compositions |
| GB1230121A (fi) * | 1967-01-27 | 1971-04-28 | ||
| FR2092794B1 (fi) * | 1970-06-19 | 1974-03-22 | Ugine Kuhlmann | |
| CH584232A5 (fi) * | 1973-07-26 | 1977-01-31 | Ciba Geigy Ag | |
| GB1489244A (en) * | 1973-09-01 | 1977-10-19 | Dynamit Nobel Ag | Organophosphonic acid esters and their partial and complete hydrolysates |
-
1983
- 1983-06-17 SE SE8303499A patent/SE450638B/sv not_active IP Right Cessation
-
1984
- 1984-06-15 US US06/705,342 patent/US4600429A/en not_active Expired - Fee Related
- 1984-06-15 EP EP84902546A patent/EP0144420B1/en not_active Expired
- 1984-06-15 DE DE8484902546T patent/DE3465999D1/de not_active Expired
- 1984-06-15 ES ES533465A patent/ES533465A0/es active Granted
- 1984-06-15 JP JP59502533A patent/JPS60501606A/ja active Granted
- 1984-06-15 IT IT48407/84A patent/IT1177801B/it active
- 1984-06-15 WO PCT/SE1984/000224 patent/WO1985000038A1/en active IP Right Grant
- 1984-06-15 AU AU30688/84A patent/AU3068884A/en not_active Abandoned
-
1985
- 1985-02-11 FI FI850555A patent/FI75576C/fi not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| JPH0442398B2 (fi) | 1992-07-13 |
| EP0144420B1 (en) | 1987-09-09 |
| AU3068884A (en) | 1985-01-11 |
| SE8303499L (sv) | 1984-12-18 |
| FI75576C (fi) | 1988-07-11 |
| WO1985000038A1 (en) | 1985-01-03 |
| US4600429A (en) | 1986-07-15 |
| JPS60501606A (ja) | 1985-09-26 |
| IT1177801B (it) | 1987-08-26 |
| FI75576B (fi) | 1988-03-31 |
| ES8505694A1 (es) | 1985-06-01 |
| FI850555A0 (fi) | 1985-02-11 |
| ES533465A0 (es) | 1985-06-01 |
| EP0144420A1 (en) | 1985-06-19 |
| SE8303499D0 (sv) | 1983-06-17 |
| DE3465999D1 (en) | 1987-10-15 |
| FI850555L (fi) | 1985-02-11 |
| IT8448407A0 (it) | 1984-06-15 |
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