NO831448L - Biocide midler inneholdende 1,2,4-triazol-1-yl-propionnitriler og fremgangsmaate ved fremstilling av disse - Google Patents
Biocide midler inneholdende 1,2,4-triazol-1-yl-propionnitriler og fremgangsmaate ved fremstilling av disseInfo
- Publication number
- NO831448L NO831448L NO831448A NO831448A NO831448L NO 831448 L NO831448 L NO 831448L NO 831448 A NO831448 A NO 831448A NO 831448 A NO831448 A NO 831448A NO 831448 L NO831448 L NO 831448L
- Authority
- NO
- Norway
- Prior art keywords
- propionitrile
- triazol
- hydronitrate
- propoxy
- phenyl
- Prior art date
Links
- -1 1,2,4-TRIAZOL-1-YL Chemical class 0.000 title claims description 93
- 239000003139 biocide Substances 0.000 title claims description 7
- 238000000034 method Methods 0.000 title claims description 6
- 238000002360 preparation method Methods 0.000 title description 8
- 150000001875 compounds Chemical class 0.000 claims description 43
- 239000000203 mixture Substances 0.000 claims description 23
- 230000000855 fungicidal effect Effects 0.000 claims description 17
- 239000002253 acid Substances 0.000 claims description 14
- 229910052736 halogen Inorganic materials 0.000 claims description 9
- 150000002367 halogens Chemical class 0.000 claims description 9
- 150000003839 salts Chemical class 0.000 claims description 9
- 125000001424 substituent group Chemical group 0.000 claims description 9
- 230000012010 growth Effects 0.000 claims description 7
- 239000000126 substance Substances 0.000 claims description 7
- HBLLMANMHSRYFX-UHFFFAOYSA-N 2-phenyl-2-propan-2-yloxy-3-(1,2,4-triazol-1-yl)propanenitrile Chemical compound C(C)(C)OC(C#N)(CN1N=CN=C1)C1=CC=CC=C1 HBLLMANMHSRYFX-UHFFFAOYSA-N 0.000 claims description 6
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 6
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 6
- NSPMIYGKQJPBQR-UHFFFAOYSA-N 4H-1,2,4-triazole Chemical compound C=1N=CNN=1 NSPMIYGKQJPBQR-UHFFFAOYSA-N 0.000 claims description 5
- 230000000844 anti-bacterial effect Effects 0.000 claims description 5
- 239000002904 solvent Substances 0.000 claims description 5
- AOJUGRIDXARWEW-UHFFFAOYSA-N 2-(2-chlorophenyl)-2-propoxy-3-(1,2,4-triazol-1-yl)propanenitrile Chemical compound ClC1=C(C=CC=C1)C(C#N)(CN1N=CN=C1)OCCC AOJUGRIDXARWEW-UHFFFAOYSA-N 0.000 claims description 4
- LZRCWKRIQVLGEV-UHFFFAOYSA-N 2-(4-chlorophenyl)-2-propoxy-3-(1,2,4-triazol-1-yl)propanenitrile Chemical compound ClC1=CC=C(C=C1)C(C#N)(CN1N=CN=C1)OCCC LZRCWKRIQVLGEV-UHFFFAOYSA-N 0.000 claims description 4
- AQLKAGXNFCOIEF-UHFFFAOYSA-N 2-butoxy-2-(2-chlorophenyl)-3-(1,2,4-triazol-1-yl)propanenitrile Chemical compound C(CCC)OC(C#N)(CN1N=CN=C1)C1=C(C=CC=C1)Cl AQLKAGXNFCOIEF-UHFFFAOYSA-N 0.000 claims description 4
- JLBNQPAVHAWILX-UHFFFAOYSA-N 2-butoxy-2-(2-methylphenyl)-3-(1,2,4-triazol-1-yl)propanenitrile Chemical compound CCCCOC(CN1C=NC=N1)(C#N)C1=C(C)C=CC=C1 JLBNQPAVHAWILX-UHFFFAOYSA-N 0.000 claims description 4
- RZKBBEVEXGMUQX-UHFFFAOYSA-N 2-butoxy-2-(4-chlorophenyl)-3-(1,2,4-triazol-1-yl)propanenitrile Chemical compound C(CCC)OC(C#N)(CN1N=CN=C1)C1=CC=C(C=C1)Cl RZKBBEVEXGMUQX-UHFFFAOYSA-N 0.000 claims description 4
- LMCMKKXPCROFKJ-UHFFFAOYSA-N 2-hexoxy-2-(2-methylphenyl)-3-(1,2,4-triazol-1-yl)propanenitrile Chemical compound C(CCCCC)OC(C#N)(CN1N=CN=C1)C1=C(C=CC=C1)C LMCMKKXPCROFKJ-UHFFFAOYSA-N 0.000 claims description 4
- 239000002585 base Substances 0.000 claims description 4
- NCEXELLTUMJYSI-UHFFFAOYSA-N 2-(1,2,4-triazol-1-yl)propanenitrile Chemical compound N#CC(C)N1C=NC=N1 NCEXELLTUMJYSI-UHFFFAOYSA-N 0.000 claims description 3
- YNLWGIJKQKXRCD-UHFFFAOYSA-N 2-butoxy-2-phenyl-3-(1,2,4-triazol-1-yl)propanenitrile Chemical compound C(CCC)OC(C#N)(CN1N=CN=C1)C1=CC=CC=C1 YNLWGIJKQKXRCD-UHFFFAOYSA-N 0.000 claims description 3
- KRGJHSJZUYFGAP-UHFFFAOYSA-N 2-ethoxy-2-phenyl-3-(1,2,4-triazol-1-yl)propanenitrile Chemical compound C(C)OC(C#N)(CN1N=CN=C1)C1=CC=CC=C1 KRGJHSJZUYFGAP-UHFFFAOYSA-N 0.000 claims description 3
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- 239000003513 alkali Substances 0.000 claims description 2
- 125000005279 aryl sulfonyloxy group Chemical group 0.000 claims description 2
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 2
- SNNRPYZTSWAVLD-UHFFFAOYSA-N 2-(2,4-dichlorophenyl)-2-propoxy-3-(1,2,4-triazol-1-yl)propanenitrile Chemical compound ClC1=C(C=CC(=C1)Cl)C(C#N)(CN1N=CN=C1)OCCC SNNRPYZTSWAVLD-UHFFFAOYSA-N 0.000 claims 2
- ZRZRAQYLXKKOCP-UHFFFAOYSA-N 2-(2-fluorophenyl)-2-hexoxy-3-(1,2,4-triazol-1-yl)propanenitrile Chemical compound FC1=C(C=CC=C1)C(C#N)(CN1N=CN=C1)OCCCCCC ZRZRAQYLXKKOCP-UHFFFAOYSA-N 0.000 claims 2
- QHKGLCOFVOKTQS-UHFFFAOYSA-N 2-(2-fluorophenyl)-2-propoxy-3-(1,2,4-triazol-1-yl)propanenitrile Chemical compound CCCOC(CN1C=NC=N1)(C#N)C1=C(F)C=CC=C1 QHKGLCOFVOKTQS-UHFFFAOYSA-N 0.000 claims 2
- XSNFTKDPLIHAIV-UHFFFAOYSA-N 2-(2-methylphenyl)-2-(1,2,4-triazol-1-ylmethyl)heptanenitrile Chemical compound CC1=C(C=CC=C1)C(C#N)(CN1N=CN=C1)CCCCC XSNFTKDPLIHAIV-UHFFFAOYSA-N 0.000 claims 2
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- LBMMNLDTYQWLJM-UHFFFAOYSA-N 2-(3,4-dichlorophenyl)-2-propoxy-3-(1,2,4-triazol-1-yl)propanenitrile Chemical compound ClC=1C=C(C=CC1Cl)C(C#N)(CN1N=CN=C1)OCCC LBMMNLDTYQWLJM-UHFFFAOYSA-N 0.000 claims 2
- RNBSSDSLEYLVTQ-UHFFFAOYSA-N 2-(4-methylphenyl)-2-propoxy-3-(1,2,4-triazol-1-yl)propanenitrile Chemical compound CC1=CC=C(C=C1)C(C#N)(CN1N=CN=C1)OCCC RNBSSDSLEYLVTQ-UHFFFAOYSA-N 0.000 claims 2
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- LKKZMGAWQIKAGY-UHFFFAOYSA-N 2-butoxy-2-(2-fluorophenyl)-3-(1,2,4-triazol-1-yl)propanenitrile Chemical compound CCCCOC(CN1C=NC=N1)(C#N)C1=C(F)C=CC=C1 LKKZMGAWQIKAGY-UHFFFAOYSA-N 0.000 claims 2
- BOGPMBSDWXXTSN-UHFFFAOYSA-N 2-hexoxy-2-(4-methylphenyl)-3-(1,2,4-triazol-1-yl)propanenitrile Chemical compound C(CCCCC)OC(C#N)(CN1N=CN=C1)C1=CC=C(C=C1)C BOGPMBSDWXXTSN-UHFFFAOYSA-N 0.000 claims 2
- FWAJBKIQMYTGOU-UHFFFAOYSA-N 2-phenyl-2-propoxy-3-(1,2,4-triazol-1-yl)propanenitrile Chemical compound C1(=CC=CC=C1)C(C#N)(CN1N=CN=C1)OCCC FWAJBKIQMYTGOU-UHFFFAOYSA-N 0.000 claims 2
- CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical compound [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 claims 2
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims 1
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 claims 1
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- IGPMTXLKSGUTHK-UHFFFAOYSA-N 2-(3-chlorophenyl)-2-hexoxy-3-(1,2,4-triazol-1-yl)propanenitrile Chemical compound ClC=1C=C(C=CC1)C(C#N)(CN1N=CN=C1)OCCCCCC IGPMTXLKSGUTHK-UHFFFAOYSA-N 0.000 claims 1
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- 125000000913 palmityl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 229910052625 palygorskite Inorganic materials 0.000 description 1
- FJKROLUGYXJWQN-UHFFFAOYSA-N papa-hydroxy-benzoic acid Natural products OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 1
- 229920002866 paraformaldehyde Polymers 0.000 description 1
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 1
- 125000003884 phenylalkyl group Chemical group 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000003495 polar organic solvent Substances 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 235000009566 rice Nutrition 0.000 description 1
- 230000005070 ripening Effects 0.000 description 1
- 229960004889 salicylic acid Drugs 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 230000007226 seed germination Effects 0.000 description 1
- 239000000741 silica gel Substances 0.000 description 1
- 229910002027 silica gel Inorganic materials 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 239000012312 sodium hydride Substances 0.000 description 1
- 229910000104 sodium hydride Inorganic materials 0.000 description 1
- 238000007711 solidification Methods 0.000 description 1
- 230000008023 solidification Effects 0.000 description 1
- 238000009331 sowing Methods 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 238000010186 staining Methods 0.000 description 1
- 230000001954 sterilising effect Effects 0.000 description 1
- 238000004659 sterilization and disinfection Methods 0.000 description 1
- 150000003458 sulfonic acid derivatives Chemical class 0.000 description 1
- 230000009897 systematic effect Effects 0.000 description 1
- 230000009885 systemic effect Effects 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- ILWRPSCZWQJDMK-UHFFFAOYSA-N triethylazanium;chloride Chemical compound Cl.CCN(CC)CC ILWRPSCZWQJDMK-UHFFFAOYSA-N 0.000 description 1
- 244000045561 useful plants Species 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 230000009105 vegetative growth Effects 0.000 description 1
- 230000017260 vegetative to reproductive phase transition of meristem Effects 0.000 description 1
- 230000003442 weekly effect Effects 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/12—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
-
- 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
- A01N43/647—Triazoles; Hydrogenated triazoles
- A01N43/653—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C255/00—Carboxylic acid nitriles
-
- 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
- C07D233/56—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 only hydrogen atoms or radicals containing only hydrogen and carbon atoms, attached to ring carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
- C07D249/02—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
- C07D249/08—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
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)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE3216301A DE3216301A1 (de) | 1982-04-26 | 1982-04-26 | 1,2,4-triazol-1-yl-propionitrile, verfahren zur herstellung dieser verbindungen sowie diese enthaltende biozide mittel |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| NO831448L true NO831448L (no) | 1983-10-27 |
Family
ID=6162445
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO831448A NO831448L (no) | 1982-04-26 | 1983-04-25 | Biocide midler inneholdende 1,2,4-triazol-1-yl-propionnitriler og fremgangsmaate ved fremstilling av disse |
Country Status (35)
| Country | Link |
|---|---|
| JP (1) | JPS58189172A (xx) |
| KR (1) | KR840004413A (xx) |
| AT (1) | AT382293B (xx) |
| AU (1) | AU568295B2 (xx) |
| BE (1) | BE896558A (xx) |
| BR (1) | BR8302107A (xx) |
| CA (1) | CA1195992A (xx) |
| CH (1) | CH653024A5 (xx) |
| CS (1) | CS244127B2 (xx) |
| DD (1) | DD212641A5 (xx) |
| DE (1) | DE3216301A1 (xx) |
| DK (1) | DK84283A (xx) |
| EG (1) | EG16141A (xx) |
| ES (1) | ES8401050A1 (xx) |
| FI (1) | FI830994L (xx) |
| FR (1) | FR2525596B1 (xx) |
| GB (1) | GB2119374B (xx) |
| GR (1) | GR78840B (xx) |
| HU (1) | HU189649B (xx) |
| IL (1) | IL68425A (xx) |
| IT (1) | IT1164185B (xx) |
| LU (1) | LU84771A1 (xx) |
| MA (1) | MA19779A1 (xx) |
| NL (1) | NL8300748A (xx) |
| NO (1) | NO831448L (xx) |
| PH (1) | PH21063A (xx) |
| PL (1) | PL135247B1 (xx) |
| PT (1) | PT76582B (xx) |
| RO (1) | RO86358B1 (xx) |
| SE (1) | SE8302118L (xx) |
| SU (1) | SU1264830A3 (xx) |
| TR (1) | TR21783A (xx) |
| YU (1) | YU55383A (xx) |
| ZA (1) | ZA832941B (xx) |
| ZW (1) | ZW9483A1 (xx) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1058694A (zh) * | 1985-10-25 | 1992-02-19 | 吴羽化学工业株式会社 | 含1，2，4-三唑-3-甲酰胺的除草组合物及用该组合物控制杂草的方法 |
| US5087635A (en) * | 1986-07-02 | 1992-02-11 | Rohm And Haas Company | Alpha-aryl-alpha-phenylethyl-1H-1,2,4-triazole-1-propanenitriles |
| CA1321588C (en) * | 1986-07-02 | 1993-08-24 | Katherine Eleanor Flynn | Alpha-aryl-alpha-phenylethyl-1h-1,2,4-triazole-1- propanenitriles |
| JPH0778045B2 (ja) * | 1987-03-19 | 1995-08-23 | 呉羽化学工業株式会社 | １，５−ジフエニル−１ｈ−１，２，４−トリアゾ−ル−３−カルボン酸アミド誘導体及び該誘導体を含有する除草剤 |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| SE7600674L (sv) * | 1975-02-05 | 1976-08-06 | Rohm & Haas | Fungicider |
| US4167576A (en) * | 1977-10-06 | 1979-09-11 | Rohm And Haas Company | Cyanoaralkylheterocyclic compounds |
| AU3620178A (en) * | 1978-05-17 | 1979-11-22 | Rohm & Haas | 1,2,4-triazole fungicides |
| DE2846127A1 (de) * | 1978-10-23 | 1980-04-30 | Basf Ag | 1,2,4-triazol-1-yl-verbindungen, ihre hersttellung und verwendung als fungizide |
| GB2104065B (en) * | 1981-06-04 | 1985-11-06 | Ciba Geigy Ag | Heterocyclyl-substituted mandelic acid compounds and mandelonitriles and their use for combating microorganisms |
| EP0099165A1 (en) * | 1982-03-23 | 1984-01-25 | Imperial Chemical Industries Plc | Triazole and imidazole compounds, process for their preparation and their use as fungicides and plant growth regulators, and intermediates for their synthesis |
-
1982
- 1982-04-26 DE DE3216301A patent/DE3216301A1/de not_active Withdrawn
-
1983
- 1983-02-24 DK DK84283A patent/DK84283A/da not_active Application Discontinuation
- 1983-02-28 NL NL8300748A patent/NL8300748A/nl not_active Application Discontinuation
- 1983-03-08 YU YU00553/83A patent/YU55383A/xx unknown
- 1983-03-22 ES ES520847A patent/ES8401050A1/es not_active Expired
- 1983-03-23 FI FI830994A patent/FI830994L/fi not_active Application Discontinuation
- 1983-04-14 SU SU833575411A patent/SU1264830A3/ru active
- 1983-04-14 CS CS832691A patent/CS244127B2/cs unknown
- 1983-04-15 SE SE8302118A patent/SE8302118L/xx unknown
- 1983-04-17 IL IL68425A patent/IL68425A/xx unknown
- 1983-04-18 IT IT20653/83A patent/IT1164185B/it active
- 1983-04-20 JP JP58068475A patent/JPS58189172A/ja active Granted
- 1983-04-21 AT AT0145783A patent/AT382293B/de not_active IP Right Cessation
- 1983-04-21 PT PT76582A patent/PT76582B/pt unknown
- 1983-04-22 RO RO110752A patent/RO86358B1/ro unknown
- 1983-04-22 PL PL1983241602A patent/PL135247B1/pl unknown
- 1983-04-24 EG EG254/83A patent/EG16141A/xx active
- 1983-04-25 TR TR21783A patent/TR21783A/xx unknown
- 1983-04-25 HU HU831419A patent/HU189649B/hu unknown
- 1983-04-25 MA MA19999A patent/MA19779A1/fr unknown
- 1983-04-25 KR KR1019830001739A patent/KR840004413A/ko not_active Application Discontinuation
- 1983-04-25 CH CH2206/83A patent/CH653024A5/de not_active IP Right Cessation
- 1983-04-25 GB GB08311220A patent/GB2119374B/en not_active Expired
- 1983-04-25 BR BR8302107A patent/BR8302107A/pt unknown
- 1983-04-25 LU LU84771A patent/LU84771A1/de unknown
- 1983-04-25 NO NO831448A patent/NO831448L/no unknown
- 1983-04-25 CA CA000426644A patent/CA1195992A/en not_active Expired
- 1983-04-25 FR FR8306728A patent/FR2525596B1/fr not_active Expired
- 1983-04-25 BE BE0/210622A patent/BE896558A/fr not_active IP Right Cessation
- 1983-04-25 GR GR71183A patent/GR78840B/el unknown
- 1983-04-25 DD DD83250186A patent/DD212641A5/de unknown
- 1983-04-26 PH PH28818A patent/PH21063A/en unknown
- 1983-04-26 ZW ZW94/83A patent/ZW9483A1/xx unknown
- 1983-04-26 AU AU13919/83A patent/AU568295B2/en not_active Ceased
- 1983-04-26 ZA ZA832941A patent/ZA832941B/xx unknown
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