DE2910237C2 - Isothiuroniumphosphite, ihre Herstellung und ihre Zusammensetzung für den Pflanzenschutz - Google Patents
Isothiuroniumphosphite, ihre Herstellung und ihre Zusammensetzung für den PflanzenschutzInfo
- Publication number
- DE2910237C2 DE2910237C2 DE2910237A DE2910237A DE2910237C2 DE 2910237 C2 DE2910237 C2 DE 2910237C2 DE 2910237 A DE2910237 A DE 2910237A DE 2910237 A DE2910237 A DE 2910237A DE 2910237 C2 DE2910237 C2 DE 2910237C2
- Authority
- DE
- Germany
- Prior art keywords
- deep
- alkyl
- formula
- isothiuronium
- phosphites
- 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.)
- Expired
Links
- YTAUXQXYUZTHAT-UHFFFAOYSA-N NC(S)=N.NC(S)=N.NC(S)=N.OP(O)O Chemical class NC(S)=N.NC(S)=N.NC(S)=N.OP(O)O YTAUXQXYUZTHAT-UHFFFAOYSA-N 0.000 title claims description 11
- 239000000203 mixture Substances 0.000 title claims description 11
- 238000000034 method Methods 0.000 claims description 11
- 238000002360 preparation method Methods 0.000 claims description 10
- -1 isothiuronium halide Chemical class 0.000 claims description 9
- 229910052739 hydrogen Inorganic materials 0.000 claims description 8
- 239000001257 hydrogen Substances 0.000 claims description 8
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 7
- OJMIONKXNSYLSR-UHFFFAOYSA-N phosphorous acid Chemical compound OP(O)O OJMIONKXNSYLSR-UHFFFAOYSA-N 0.000 claims description 7
- 239000004480 active ingredient Substances 0.000 claims description 5
- 125000000217 alkyl group Chemical group 0.000 claims description 5
- 125000001424 substituent group Chemical group 0.000 claims description 5
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 4
- 201000010099 disease Diseases 0.000 claims description 3
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims description 3
- 241000894006 Bacteria Species 0.000 claims description 2
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 2
- 239000005977 Ethylene Substances 0.000 claims description 2
- 241000233866 Fungi Species 0.000 claims description 2
- 239000000969 carrier Substances 0.000 claims description 2
- 229910052736 halogen Inorganic materials 0.000 claims description 2
- 150000002367 halogens Chemical group 0.000 claims description 2
- 239000000546 pharmaceutical excipient Substances 0.000 claims description 2
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 claims description 2
- 150000002431 hydrogen Chemical class 0.000 claims 1
- 150000001875 compounds Chemical class 0.000 description 13
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 12
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 12
- UMGDCJDMYOKAJW-UHFFFAOYSA-N thiourea Chemical compound NC(N)=S UMGDCJDMYOKAJW-UHFFFAOYSA-N 0.000 description 10
- 238000006243 chemical reaction Methods 0.000 description 8
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 6
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Natural products NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 5
- 239000002244 precipitate Substances 0.000 description 5
- 239000000047 product Substances 0.000 description 5
- 239000007787 solid Substances 0.000 description 5
- 238000000921 elemental analysis Methods 0.000 description 4
- 230000000855 fungicidal effect Effects 0.000 description 4
- AQSJGOWTSHOLKH-UHFFFAOYSA-N phosphite(3-) Chemical class [O-]P([O-])[O-] AQSJGOWTSHOLKH-UHFFFAOYSA-N 0.000 description 4
- 230000015572 biosynthetic process Effects 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- 230000000704 physical effect Effects 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 238000003786 synthesis reaction Methods 0.000 description 3
- ISIJQEHRDSCQIU-UHFFFAOYSA-N tert-butyl 2,7-diazaspiro[4.5]decane-7-carboxylate Chemical class C1N(C(=O)OC(C)(C)C)CCCC11CNCC1 ISIJQEHRDSCQIU-UHFFFAOYSA-N 0.000 description 3
- FZRJLBJACDITKM-UHFFFAOYSA-N 1,3,2-dioxaphospholane Chemical compound C1COPO1 FZRJLBJACDITKM-UHFFFAOYSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- 238000005481 NMR spectroscopy Methods 0.000 description 2
- WQDUMFSSJAZKTM-UHFFFAOYSA-N Sodium methoxide Chemical compound [Na+].[O-]C WQDUMFSSJAZKTM-UHFFFAOYSA-N 0.000 description 2
- 230000000844 anti-bacterial effect Effects 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- CZHYKKAKFWLGJO-UHFFFAOYSA-N dimethyl phosphite Chemical compound COP([O-])OC CZHYKKAKFWLGJO-UHFFFAOYSA-N 0.000 description 2
- KRZGKJJPEOUIBI-UHFFFAOYSA-N hydron;thiourea;iodide Chemical compound I.NC(S)=N KRZGKJJPEOUIBI-UHFFFAOYSA-N 0.000 description 2
- 150000004694 iodide salts Chemical class 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- SDDKIZNHOCEXTF-UHFFFAOYSA-N methyl carbamimidothioate Chemical compound CSC(N)=N SDDKIZNHOCEXTF-UHFFFAOYSA-N 0.000 description 2
- DGVNWNYQSOYWKZ-UHFFFAOYSA-N methyl dihydrogen phosphite Chemical class COP(O)O DGVNWNYQSOYWKZ-UHFFFAOYSA-N 0.000 description 2
- 231100000208 phytotoxic Toxicity 0.000 description 2
- 230000000885 phytotoxic effect Effects 0.000 description 2
- 239000012429 reaction media Substances 0.000 description 2
- 239000011541 reaction mixture Substances 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- SZUVGFMDDVSKSI-WIFOCOSTSA-N (1s,2s,3s,5r)-1-(carboxymethyl)-3,5-bis[(4-phenoxyphenyl)methyl-propylcarbamoyl]cyclopentane-1,2-dicarboxylic acid Chemical compound O=C([C@@H]1[C@@H]([C@](CC(O)=O)([C@H](C(=O)N(CCC)CC=2C=CC(OC=3C=CC=CC=3)=CC=2)C1)C(O)=O)C(O)=O)N(CCC)CC(C=C1)=CC=C1OC1=CC=CC=C1 SZUVGFMDDVSKSI-WIFOCOSTSA-N 0.000 description 1
- GHYOCDFICYLMRF-UTIIJYGPSA-N (2S,3R)-N-[(2S)-3-(cyclopenten-1-yl)-1-[(2R)-2-methyloxiran-2-yl]-1-oxopropan-2-yl]-3-hydroxy-3-(4-methoxyphenyl)-2-[[(2S)-2-[(2-morpholin-4-ylacetyl)amino]propanoyl]amino]propanamide Chemical compound C1(=CCCC1)C[C@@H](C(=O)[C@@]1(OC1)C)NC([C@H]([C@@H](C1=CC=C(C=C1)OC)O)NC([C@H](C)NC(CN1CCOCC1)=O)=O)=O GHYOCDFICYLMRF-UTIIJYGPSA-N 0.000 description 1
- QFLWZFQWSBQYPS-AWRAUJHKSA-N (3S)-3-[[(2S)-2-[[(2S)-2-[5-[(3aS,6aR)-2-oxo-1,3,3a,4,6,6a-hexahydrothieno[3,4-d]imidazol-4-yl]pentanoylamino]-3-methylbutanoyl]amino]-3-(4-hydroxyphenyl)propanoyl]amino]-4-[1-bis(4-chlorophenoxy)phosphorylbutylamino]-4-oxobutanoic acid Chemical compound CCCC(NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)CCCCC1SC[C@@H]2NC(=O)N[C@H]12)C(C)C)P(=O)(Oc1ccc(Cl)cc1)Oc1ccc(Cl)cc1 QFLWZFQWSBQYPS-AWRAUJHKSA-N 0.000 description 1
- UNILWMWFPHPYOR-KXEYIPSPSA-M 1-[6-[2-[3-[3-[3-[2-[2-[3-[[2-[2-[[(2r)-1-[[2-[[(2r)-1-[3-[2-[2-[3-[[2-(2-amino-2-oxoethoxy)acetyl]amino]propoxy]ethoxy]ethoxy]propylamino]-3-hydroxy-1-oxopropan-2-yl]amino]-2-oxoethyl]amino]-3-[(2r)-2,3-di(hexadecanoyloxy)propyl]sulfanyl-1-oxopropan-2-yl Chemical compound O=C1C(SCCC(=O)NCCCOCCOCCOCCCNC(=O)COCC(=O)N[C@@H](CSC[C@@H](COC(=O)CCCCCCCCCCCCCCC)OC(=O)CCCCCCCCCCCCCCC)C(=O)NCC(=O)N[C@H](CO)C(=O)NCCCOCCOCCOCCCNC(=O)COCC(N)=O)CC(=O)N1CCNC(=O)CCCCCN\1C2=CC=C(S([O-])(=O)=O)C=C2CC/1=C/C=C/C=C/C1=[N+](CC)C2=CC=C(S([O-])(=O)=O)C=C2C1 UNILWMWFPHPYOR-KXEYIPSPSA-M 0.000 description 1
- QIMRRNPSHOEBRE-UHFFFAOYSA-N CCCCCCCCCCCCNC(SCC)=N.CCCCCCCCCCCCNC(SCC)=N.COP(O)O Chemical compound CCCCCCCCCCCCNC(SCC)=N.CCCCCCCCCCCCNC(SCC)=N.COP(O)O QIMRRNPSHOEBRE-UHFFFAOYSA-N 0.000 description 1
- OSBXGLCAOCDMAR-UHFFFAOYSA-N COP(O)O.CSC(N)=N.CSC(N)=N Chemical compound COP(O)O.CSC(N)=N.CSC(N)=N OSBXGLCAOCDMAR-UHFFFAOYSA-N 0.000 description 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
- 238000004566 IR spectroscopy Methods 0.000 description 1
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 1
- GDOIQLNSIAMNMA-UHFFFAOYSA-N [I-].C(C)SC(NCCCCCCCCCCCC)=[NH2+] Chemical compound [I-].C(C)SC(NCCCCCCCCCCCC)=[NH2+] GDOIQLNSIAMNMA-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 150000001351 alkyl iodides Chemical class 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- RBHJBMIOOPYDBQ-UHFFFAOYSA-N carbon dioxide;propan-2-one Chemical compound O=C=O.CC(C)=O RBHJBMIOOPYDBQ-UHFFFAOYSA-N 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 229940125904 compound 1 Drugs 0.000 description 1
- 229940125797 compound 12 Drugs 0.000 description 1
- 229940126543 compound 14 Drugs 0.000 description 1
- LXCYSACZTOKNNS-UHFFFAOYSA-N diethoxy(oxo)phosphanium Chemical compound CCO[P+](=O)OCC LXCYSACZTOKNNS-UHFFFAOYSA-N 0.000 description 1
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 1
- HWSUUGHIDOOOOJ-UHFFFAOYSA-N dioxaphosphinane Chemical compound C1COOPC1 HWSUUGHIDOOOOJ-UHFFFAOYSA-N 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 230000002538 fungal effect Effects 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- INQOMBQAUSQDDS-UHFFFAOYSA-N iodomethane Chemical compound IC INQOMBQAUSQDDS-UHFFFAOYSA-N 0.000 description 1
- NNBBQNFHCVVQHZ-UHFFFAOYSA-N methyl carbamimidothioate;sulfuric acid Chemical compound CSC(N)=N.OS(O)(=O)=O NNBBQNFHCVVQHZ-UHFFFAOYSA-N 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- VXTFGYMINLXJPW-UHFFFAOYSA-N phosphinane Chemical compound C1CCPCC1 VXTFGYMINLXJPW-UHFFFAOYSA-N 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 150000003585 thioureas Chemical class 0.000 description 1
- 238000005292 vacuum distillation 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
- A01N57/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds
- A01N57/10—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-oxygen bonds or phosphorus-to-sulfur bonds
- A01N57/12—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-oxygen bonds or phosphorus-to-sulfur bonds containing acyclic or cycloaliphatic radicals
-
- 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
- A01N59/00—Biocides, pest repellants or attractants, or plant growth regulators containing elements or inorganic compounds
- A01N59/26—Phosphorus; Compounds thereof
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Wood Science & Technology (AREA)
- General Health & Medical Sciences (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Zoology (AREA)
- Dentistry (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (AREA)
- Engineering & Computer Science (AREA)
- Environmental Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Inorganic Chemistry (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Nitrogen- Or Sulfur-Containing Heterocyclic Ring Compounds With Rings Of Six Or More Members (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR7808237A FR2419675A1 (fr) | 1978-03-16 | 1978-03-16 | Compositions fongicides a base de phosphites d'isothiouronium |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| DE2910237A1 DE2910237A1 (de) | 1979-10-04 |
| DE2910237C2 true DE2910237C2 (de) | 1987-04-09 |
Family
ID=9206121
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE2910237A Expired DE2910237C2 (de) | 1978-03-16 | 1979-03-15 | Isothiuroniumphosphite, ihre Herstellung und ihre Zusammensetzung für den Pflanzenschutz |
Country Status (36)
| Country | Link |
|---|---|
| US (1) | US4382928A (pt-PT) |
| JP (2) | JPS54130521A (pt-PT) |
| AR (1) | AR220747A1 (pt-PT) |
| AT (1) | AT374483B (pt-PT) |
| AU (1) | AU530215B2 (pt-PT) |
| BE (1) | BE874907A (pt-PT) |
| BG (1) | BG32264A3 (pt-PT) |
| BR (1) | BR7901620A (pt-PT) |
| CA (1) | CA1118785A (pt-PT) |
| CH (1) | CH640700A5 (pt-PT) |
| CS (1) | CS208492B2 (pt-PT) |
| CU (1) | CU35057A (pt-PT) |
| DD (1) | DD142282A5 (pt-PT) |
| DE (1) | DE2910237C2 (pt-PT) |
| DK (1) | DK106679A (pt-PT) |
| EG (1) | EG14428A (pt-PT) |
| ES (2) | ES478641A1 (pt-PT) |
| FR (1) | FR2419675A1 (pt-PT) |
| GB (1) | GB2016926B (pt-PT) |
| GR (1) | GR68033B (pt-PT) |
| HU (1) | HU182985B (pt-PT) |
| IE (1) | IE48734B1 (pt-PT) |
| IL (1) | IL56884A (pt-PT) |
| IT (1) | IT1162483B (pt-PT) |
| LU (1) | LU81055A1 (pt-PT) |
| NL (1) | NL188831C (pt-PT) |
| NZ (1) | NZ189907A (pt-PT) |
| OA (1) | OA06216A (pt-PT) |
| PH (1) | PH16323A (pt-PT) |
| PL (1) | PL214137A1 (pt-PT) |
| PT (1) | PT69356A (pt-PT) |
| RO (1) | RO79037A (pt-PT) |
| SE (1) | SE446929B (pt-PT) |
| SU (1) | SU952107A3 (pt-PT) |
| TR (1) | TR19935A (pt-PT) |
| ZA (1) | ZA791224B (pt-PT) |
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2457873A1 (fr) * | 1978-03-16 | 1980-12-26 | Rhone Poulenc Agrochimie | Compositions fongicides a base de phosphites d'isothiouronium |
| FR2451164A2 (fr) * | 1978-03-16 | 1980-10-10 | Rhone Poulenc Agrochimie | Compositions fongicides a base de phosphites d'isothiouronium |
| FR2655816B1 (fr) * | 1989-12-14 | 1994-04-29 | Rhone Poulenc Agrochimie | Granules dispersables de produits fongicides. |
| US5133891A (en) * | 1990-04-27 | 1992-07-28 | Rhone Poulenc Ag Co. | Treatment of plants for frost protection |
| JPH0478737U (pt-PT) * | 1990-11-19 | 1992-07-09 | ||
| WO1998013036A1 (en) * | 1996-09-26 | 1998-04-02 | Meditor Pharmaceuticals Ltd. | Pharmaceutical compositions comprising s-alkylisothiouronium derivatives |
| PT1315505E (pt) * | 2000-09-05 | 2008-01-28 | Meditor Pharmaceuticals Ltd | Composições farmacêuticas para a dor de cabeça, enxaqueca, náusea e emese |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2456627C2 (de) | 1973-12-14 | 1984-05-10 | PEPRO - Société pour le Développement et la Vente de Spécialités Chimiques, Lyon | Fungizide Mittel auf der Basis von Phosphonsäureestern |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4119724A (en) * | 1973-11-26 | 1978-10-10 | Pepro | Fungicidal compositions containing phosphorous acid and derivatives thereof |
| FR2254276B1 (pt-PT) * | 1973-12-14 | 1977-03-04 | Philagro Sa | |
| FR2380286A1 (fr) * | 1977-02-14 | 1978-09-08 | Philagro Sa | Nouveaux derives de phosphites d'hydrazinium |
-
1978
- 1978-03-16 FR FR7808237A patent/FR2419675A1/fr active Granted
-
1979
- 1979-03-07 GR GR58536A patent/GR68033B/el unknown
- 1979-03-13 PH PH22281A patent/PH16323A/en unknown
- 1979-03-14 NZ NZ189907A patent/NZ189907A/xx unknown
- 1979-03-15 ZA ZA791224A patent/ZA791224B/xx unknown
- 1979-03-15 AT AT0197179A patent/AT374483B/de not_active IP Right Cessation
- 1979-03-15 GB GB7909200A patent/GB2016926B/en not_active Expired
- 1979-03-15 JP JP3052079A patent/JPS54130521A/ja active Granted
- 1979-03-15 DE DE2910237A patent/DE2910237C2/de not_active Expired
- 1979-03-15 IL IL56884A patent/IL56884A/xx unknown
- 1979-03-15 OA OA56767A patent/OA06216A/xx unknown
- 1979-03-15 PT PT69356A patent/PT69356A/pt unknown
- 1979-03-15 NL NLAANVRAGE7902056,A patent/NL188831C/xx not_active IP Right Cessation
- 1979-03-15 TR TR19935A patent/TR19935A/xx unknown
- 1979-03-15 IT IT48373/79A patent/IT1162483B/it active
- 1979-03-15 AU AU45162/79A patent/AU530215B2/en not_active Ceased
- 1979-03-15 ES ES478641A patent/ES478641A1/es not_active Expired
- 1979-03-15 AR AR275811A patent/AR220747A1/es active
- 1979-03-15 RO RO7996910A patent/RO79037A/ro unknown
- 1979-03-15 CH CH245679A patent/CH640700A5/fr not_active IP Right Cessation
- 1979-03-15 BR BR7901620A patent/BR7901620A/pt unknown
- 1979-03-15 SE SE7902354A patent/SE446929B/sv not_active IP Right Cessation
- 1979-03-15 DK DK106679A patent/DK106679A/da unknown
- 1979-03-15 CA CA000323456A patent/CA1118785A/en not_active Expired
- 1979-03-15 PL PL21413779A patent/PL214137A1/xx unknown
- 1979-03-16 BE BE0/194072A patent/BE874907A/xx not_active IP Right Cessation
- 1979-03-16 LU LU81055A patent/LU81055A1/fr unknown
- 1979-03-16 CS CS791772A patent/CS208492B2/cs unknown
- 1979-03-16 CU CU7935057A patent/CU35057A/es unknown
- 1979-03-16 HU HU79PI669A patent/HU182985B/hu unknown
- 1979-03-16 DD DD79211633A patent/DD142282A5/de unknown
- 1979-03-16 BG BG042905A patent/BG32264A3/xx unknown
- 1979-03-17 EG EG178/79A patent/EG14428A/xx active
- 1979-05-04 ES ES480224A patent/ES480224A1/es not_active Expired
- 1979-08-08 IE IE614/79A patent/IE48734B1/en not_active IP Right Cessation
-
1980
- 1980-03-11 SU SU802891756A patent/SU952107A3/ru active
- 1980-03-18 US US06/131,400 patent/US4382928A/en not_active Expired - Lifetime
-
1987
- 1987-05-12 JP JP62115686A patent/JPS62281886A/ja active Pending
Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2456627C2 (de) | 1973-12-14 | 1984-05-10 | PEPRO - Société pour le Développement et la Vente de Spécialités Chimiques, Lyon | Fungizide Mittel auf der Basis von Phosphonsäureestern |
Non-Patent Citations (1)
| Title |
|---|
| NICHTS-ERMITTELT |
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