DE2531625C2 - - Google Patents
Info
- Publication number
- DE2531625C2 DE2531625C2 DE2531625A DE2531625A DE2531625C2 DE 2531625 C2 DE2531625 C2 DE 2531625C2 DE 2531625 A DE2531625 A DE 2531625A DE 2531625 A DE2531625 A DE 2531625A DE 2531625 C2 DE2531625 C2 DE 2531625C2
- Authority
- DE
- Germany
- Prior art keywords
- hydantoin
- dichlorophenyl
- compositions
- isopropylcarbamoyl
- active ingredient
- 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 - Lifetime
Links
- TWFZGCMQGLPBSX-UHFFFAOYSA-N carbendazim Chemical group C1=CC=C2NC(NC(=O)OC)=NC2=C1 TWFZGCMQGLPBSX-UHFFFAOYSA-N 0.000 claims description 11
- 230000000855 fungicidal effect Effects 0.000 claims description 8
- 239000000417 fungicide Substances 0.000 claims description 6
- RIOXQFHNBCKOKP-UHFFFAOYSA-N benomyl Chemical compound C1=CC=C2N(C(=O)NCCCC)C(NC(=O)OC)=NC2=C1 RIOXQFHNBCKOKP-UHFFFAOYSA-N 0.000 claims description 5
- QGHREAKMXXNCOA-UHFFFAOYSA-N thiophanate-methyl Chemical compound COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC QGHREAKMXXNCOA-UHFFFAOYSA-N 0.000 claims description 5
- 150000001469 hydantoins Chemical class 0.000 claims description 2
- 239000000203 mixture Substances 0.000 description 15
- 230000000694 effects Effects 0.000 description 12
- 235000013339 cereals Nutrition 0.000 description 11
- ONUFESLQCSAYKA-UHFFFAOYSA-N iprodione Chemical compound O=C1N(C(=O)NC(C)C)CC(=O)N1C1=CC(Cl)=CC(Cl)=C1 ONUFESLQCSAYKA-UHFFFAOYSA-N 0.000 description 9
- 239000004480 active ingredient Substances 0.000 description 8
- -1 alkyl radicals Chemical class 0.000 description 8
- 125000004432 carbon atom Chemical group C* 0.000 description 6
- 239000003085 diluting agent Substances 0.000 description 5
- 239000006013 carbendazim Substances 0.000 description 4
- 239000007787 solid Substances 0.000 description 4
- 238000004659 sterilization and disinfection Methods 0.000 description 4
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 3
- 241000228453 Pyrenophora Species 0.000 description 3
- 239000000839 emulsion Substances 0.000 description 3
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 3
- 244000045947 parasite Species 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- 239000005995 Aluminium silicate Substances 0.000 description 2
- 244000075850 Avena orientalis Species 0.000 description 2
- 235000007319 Avena orientalis Nutrition 0.000 description 2
- 241000219112 Cucumis Species 0.000 description 2
- 235000015510 Cucumis melo subsp melo Nutrition 0.000 description 2
- 241000223221 Fusarium oxysporum Species 0.000 description 2
- 240000005979 Hordeum vulgare Species 0.000 description 2
- 235000007340 Hordeum vulgare Nutrition 0.000 description 2
- 241001459558 Monographella nivalis Species 0.000 description 2
- 235000012211 aluminium silicate Nutrition 0.000 description 2
- 230000009286 beneficial effect Effects 0.000 description 2
- MITFXPHMIHQXPI-UHFFFAOYSA-N benzoxaprofen Natural products N=1C2=CC(C(C(O)=O)C)=CC=C2OC=1C1=CC=C(Cl)C=C1 MITFXPHMIHQXPI-UHFFFAOYSA-N 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 239000002270 dispersing agent Substances 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 125000004430 oxygen atom Chemical group O* 0.000 description 2
- 235000010482 polyoxyethylene sorbitan monooleate Nutrition 0.000 description 2
- 229920000053 polysorbate 80 Polymers 0.000 description 2
- MTQKMPGBALVEDL-ZPCKWCKBSA-N (z,12r)-12-hydroxy-2-sulfooctadec-9-enoic acid Chemical compound CCCCCC[C@@H](O)C\C=C/CCCCCCC(C(O)=O)S(O)(=O)=O MTQKMPGBALVEDL-ZPCKWCKBSA-N 0.000 description 1
- 241001120669 Colletotrichum lindemuthianum Species 0.000 description 1
- 240000008067 Cucumis sativus Species 0.000 description 1
- 235000010799 Cucumis sativus var sativus Nutrition 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- 240000009088 Fragaria x ananassa Species 0.000 description 1
- 241000233866 Fungi Species 0.000 description 1
- 241000223194 Fusarium culmorum Species 0.000 description 1
- 239000005867 Iprodione Substances 0.000 description 1
- 239000005909 Kieselgur Substances 0.000 description 1
- 241000896238 Oidium Species 0.000 description 1
- 241000736122 Parastagonospora nodorum Species 0.000 description 1
- 244000046052 Phaseolus vulgaris Species 0.000 description 1
- 235000010627 Phaseolus vulgaris Nutrition 0.000 description 1
- 241000221300 Puccinia Species 0.000 description 1
- 241000520647 Pyrenophora avenae Species 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- FJJCIZWZNKZHII-UHFFFAOYSA-N [4,6-bis(cyanoamino)-1,3,5-triazin-2-yl]cyanamide Chemical compound N#CNC1=NC(NC#N)=NC(NC#N)=N1 FJJCIZWZNKZHII-UHFFFAOYSA-N 0.000 description 1
- CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical group [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 description 1
- 230000002745 absorbent Effects 0.000 description 1
- 239000002250 absorbent Substances 0.000 description 1
- 239000013543 active substance Substances 0.000 description 1
- 239000002671 adjuvant Substances 0.000 description 1
- 125000004429 atom Chemical group 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
- 230000015572 biosynthetic process Effects 0.000 description 1
- 235000013532 brandy Nutrition 0.000 description 1
- 239000001506 calcium phosphate Substances 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 239000003245 coal Substances 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 239000013068 control sample Substances 0.000 description 1
- 239000007799 cork Substances 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- YDEXUEFDPVHGHE-GGMCWBHBSA-L disodium;(2r)-3-(2-hydroxy-3-methoxyphenyl)-2-[2-methoxy-4-(3-sulfonatopropyl)phenoxy]propane-1-sulfonate Chemical compound [Na+].[Na+].COC1=CC=CC(C[C@H](CS([O-])(=O)=O)OC=2C(=CC(CCCS([O-])(=O)=O)=CC=2)OC)=C1O YDEXUEFDPVHGHE-GGMCWBHBSA-L 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 235000013399 edible fruits Nutrition 0.000 description 1
- 239000003792 electrolyte Substances 0.000 description 1
- 239000004495 emulsifiable concentrate Substances 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 238000006266 etherification reaction Methods 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 125000005843 halogen group Chemical group 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 239000000395 magnesium oxide Substances 0.000 description 1
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 1
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 description 1
- 239000004570 mortar (masonry) Substances 0.000 description 1
- 235000015097 nutrients Nutrition 0.000 description 1
- 230000003032 phytopathogenic effect Effects 0.000 description 1
- 239000000244 polyoxyethylene sorbitan monooleate Substances 0.000 description 1
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 1
- 150000003254 radicals Chemical class 0.000 description 1
- 238000007873 sieving Methods 0.000 description 1
- 239000008247 solid mixture Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- QORWJWZARLRLPR-UHFFFAOYSA-H tricalcium bis(phosphate) Chemical compound [Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O QORWJWZARLRLPR-UHFFFAOYSA-H 0.000 description 1
- 229940078499 tricalcium phosphate Drugs 0.000 description 1
- 229910000391 tricalcium phosphate Inorganic materials 0.000 description 1
- 235000019731 tricalcium phosphate Nutrition 0.000 description 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 239000000080 wetting agent Substances 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
- 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<
- A01N47/38—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N< containing the group >N—CO—N< where at least one nitrogen atom is part of a heterocyclic ring; Thio analogues thereof
Landscapes
- 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)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR7424511A FR2278262A1 (fr) | 1974-07-15 | 1974-07-15 | Nouvelles compositions fongicides |
| FR7517425A FR2312954A2 (fr) | 1975-06-04 | 1975-06-04 | Nouvelles compositions fongicides |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| DE2531625A1 DE2531625A1 (de) | 1976-01-29 |
| DE2531625C2 true DE2531625C2 (en, 2012) | 1991-07-18 |
Family
ID=26218435
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE19752531625 Granted DE2531625A1 (de) | 1974-07-15 | 1975-07-15 | Neue fungizide zusammensetzungen |
Country Status (14)
| Country | Link |
|---|---|
| US (1) | US4044145A (en, 2012) |
| JP (1) | JPS609002B2 (en, 2012) |
| AR (1) | AR220092A1 (en, 2012) |
| BR (1) | BR7504414A (en, 2012) |
| CA (1) | CA1046403A (en, 2012) |
| CH (1) | CH597752A5 (en, 2012) |
| DE (1) | DE2531625A1 (en, 2012) |
| ES (1) | ES439421A1 (en, 2012) |
| GB (1) | GB1456488A (en, 2012) |
| HU (1) | HU172874B (en, 2012) |
| IE (1) | IE41185B1 (en, 2012) |
| IT (1) | IT1043998B (en, 2012) |
| NL (1) | NL183118C (en, 2012) |
| OA (1) | OA05041A (en, 2012) |
Families Citing this family (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| RO66706A2 (ro) * | 1977-10-01 | 1982-03-24 | Centrala Industriala De Produse Anorganice,Ro | Compozitie fungicida cu volum ultraredus |
| JPS57128608A (en) * | 1981-01-31 | 1982-08-10 | Nippon Kayaku Co Ltd | Agricultural and horticultural soil germicide |
| IT1150675B (it) * | 1981-03-20 | 1986-12-17 | Rhone Poulenc Agrochimie | Composizione fungicida a base d'iprodione |
| JPS5915951U (ja) * | 1982-07-21 | 1984-01-31 | 相模ゴム工業株式会社 | 採尿袋 |
| US4576950A (en) * | 1983-12-14 | 1986-03-18 | Safer Agro-Chem Ltd. | Alkyl pyridinium synergists for benzimidazole pesticides |
| US4859689A (en) * | 1986-10-31 | 1989-08-22 | Safer, Inc. | Synergistic fungicidal composition comprise a benzimidazole compound, an alkyl pyridinium salt, and a carrier and the use thereof to combat fungi |
| CN103535367A (zh) * | 2013-10-28 | 2014-01-29 | 中国农业大学 | 防治棉花轮纹斑病的异菌脲与福美双混配药剂 |
| CN104886107A (zh) * | 2015-06-03 | 2015-09-09 | 杭州师范大学 | 一种防治杭白菊叶枯病的复配杀菌剂 |
| CN108184876A (zh) * | 2017-12-29 | 2018-06-22 | 广东广康生化科技股份有限公司 | 含灭菌丹和异菌脲的杀菌组合物及应用 |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CH501364A (de) | 1967-04-11 | 1971-01-15 | Du Pont | Verfahren zur Bekämpfung von Pilzerkrankungen bei Pflanzen |
| IL27824A (en) | 1966-05-06 | 1971-04-28 | Du Pont | Substituted 2-aminobenzimidazoles |
| IL30778A (en) | 1967-10-30 | 1972-10-29 | Nippon Soda Co | Bis-thioureido-benzenes,their preparation,and fungicidal compositions containing them |
| DK123717B (da) * | 1968-11-25 | 1972-07-24 | Sumitomo Chemical Co | 3-(3',5'-Dihalogenphenyl)-imidazolidin-2,4-dionderivater med mirobicid virkning. |
| GB1312743A (en) | 1970-07-17 | 1973-04-04 | Rhone Poulenc Sa | Thiazolidine derivatives |
| FR2120222A5 (en) * | 1970-10-06 | 1972-08-18 | Rhone Poulenc Sa | N-acyl-hydantoin derivs - with fungicidal activity |
| FR2148868A6 (en, 2012) | 1970-10-06 | 1973-03-23 | Rhone Poulenc Sa |
-
1975
- 1975-06-30 OA OA55540A patent/OA05041A/xx unknown
- 1975-07-07 NL NLAANVRAGE7508073,A patent/NL183118C/xx not_active IP Right Cessation
- 1975-07-11 BR BR7504414*A patent/BR7504414A/pt unknown
- 1975-07-14 US US05/595,605 patent/US4044145A/en not_active Expired - Lifetime
- 1975-07-14 CA CA231,333A patent/CA1046403A/en not_active Expired
- 1975-07-14 JP JP50085414A patent/JPS609002B2/ja not_active Expired
- 1975-07-14 GB GB2948075A patent/GB1456488A/en not_active Expired
- 1975-07-14 AR AR259562A patent/AR220092A1/es active
- 1975-07-14 CH CH918775A patent/CH597752A5/xx not_active IP Right Cessation
- 1975-07-14 IE IE1556/75A patent/IE41185B1/xx unknown
- 1975-07-14 HU HU75RO00000846A patent/HU172874B/hu unknown
- 1975-07-15 IT IT25438/75A patent/IT1043998B/it active
- 1975-07-15 DE DE19752531625 patent/DE2531625A1/de active Granted
- 1975-07-15 ES ES439421A patent/ES439421A1/es not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| BR7504414A (pt) | 1976-07-06 |
| IT1043998B (it) | 1980-02-29 |
| US4044145A (en) | 1977-08-23 |
| DE2531625A1 (de) | 1976-01-29 |
| AU8302075A (en) | 1977-01-20 |
| ES439421A1 (es) | 1977-11-16 |
| CH597752A5 (en, 2012) | 1978-04-14 |
| JPS609002B2 (ja) | 1985-03-07 |
| OA05041A (fr) | 1980-12-31 |
| HU172874B (hu) | 1978-12-28 |
| GB1456488A (en) | 1976-11-24 |
| NL7508073A (nl) | 1976-01-19 |
| IE41185B1 (en) | 1979-11-07 |
| NL183118C (nl) | 1988-08-01 |
| JPS5135434A (en, 2012) | 1976-03-25 |
| AR220092A1 (es) | 1980-10-15 |
| IE41185L (en) | 1976-01-15 |
| NL183118B (nl) | 1988-03-01 |
| CA1046403A (en) | 1979-01-16 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| 8110 | Request for examination paragraph 44 | ||
| 8128 | New person/name/address of the agent |
Representative=s name: ZUMSTEIN SEN., F., DR. ASSMANN, E., DIPL.-CHEM. DR |
|
| 8172 | Supplementary division/partition in: |
Ref country code: DE Ref document number: 2560669 Format of ref document f/p: P |
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| Q171 | Divided out to: |
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| 8172 | Supplementary division/partition in: |
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| Q171 | Divided out to: |
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|
| 8125 | Change of the main classification |
Ipc: A01N 47/38 |
|
| AH | Division in |
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| D2 | Grant after examination | ||
| 8364 | No opposition during term of opposition |