DE4230955A1 - Verwendung von Thiadiazol-Verbindungen als Antifouling-Wirkstoff - Google Patents
Verwendung von Thiadiazol-Verbindungen als Antifouling-WirkstoffInfo
- Publication number
- DE4230955A1 DE4230955A1 DE4230955A DE4230955A DE4230955A1 DE 4230955 A1 DE4230955 A1 DE 4230955A1 DE 4230955 A DE4230955 A DE 4230955A DE 4230955 A DE4230955 A DE 4230955A DE 4230955 A1 DE4230955 A1 DE 4230955A1
- Authority
- DE
- Germany
- Prior art keywords
- thiadiazole
- weight
- methylsulfonyl
- thiadiazole compounds
- xylene
- 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.)
- Withdrawn
Links
- 150000004867 thiadiazoles Chemical class 0.000 title claims description 7
- 230000003373 anti-fouling effect Effects 0.000 title description 13
- 239000004480 active ingredient Substances 0.000 title description 4
- LKGIJQSLJASXHQ-UHFFFAOYSA-N 5-methylsulfonyl-3-phenyl-1,2,4-thiadiazole Chemical compound S1C(S(=O)(=O)C)=NC(C=2C=CC=CC=2)=N1 LKGIJQSLJASXHQ-UHFFFAOYSA-N 0.000 claims description 7
- 229910052736 halogen Inorganic materials 0.000 claims description 6
- 150000002367 halogens Chemical class 0.000 claims description 6
- 239000011230 binding agent Substances 0.000 claims description 5
- 238000002360 preparation method Methods 0.000 claims description 4
- 229910052739 hydrogen Inorganic materials 0.000 claims description 3
- 239000001257 hydrogen Substances 0.000 claims description 3
- 239000007787 solid Substances 0.000 claims description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 2
- 239000002519 antifouling agent Substances 0.000 claims description 2
- 239000003085 diluting agent Substances 0.000 claims description 2
- 239000006185 dispersion Substances 0.000 claims description 2
- 239000000839 emulsion Substances 0.000 claims description 2
- 239000000243 solution Substances 0.000 claims description 2
- 125000000547 substituted alkyl group Chemical group 0.000 claims description 2
- 230000001804 emulsifying effect Effects 0.000 claims 1
- 239000000463 material Substances 0.000 claims 1
- 238000009736 wetting Methods 0.000 claims 1
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 36
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 21
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 18
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 17
- 239000008096 xylene Substances 0.000 description 17
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 16
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 16
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 15
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 12
- 239000003973 paint Substances 0.000 description 12
- 239000000049 pigment Substances 0.000 description 11
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 10
- 239000004408 titanium dioxide Substances 0.000 description 10
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 9
- WQDUMFSSJAZKTM-UHFFFAOYSA-N Sodium methoxide Chemical compound [Na+].[O-]C WQDUMFSSJAZKTM-UHFFFAOYSA-N 0.000 description 8
- 150000001875 compounds Chemical class 0.000 description 8
- 239000002244 precipitate Substances 0.000 description 8
- -1 carboxy, hydroxy Chemical group 0.000 description 7
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 6
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 5
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 5
- 230000015572 biosynthetic process Effects 0.000 description 5
- QGJOPFRUJISHPQ-NJFSPNSNSA-N carbon disulfide-14c Chemical compound S=[14C]=S QGJOPFRUJISHPQ-NJFSPNSNSA-N 0.000 description 5
- INQOMBQAUSQDDS-UHFFFAOYSA-N iodomethane Chemical compound IC INQOMBQAUSQDDS-UHFFFAOYSA-N 0.000 description 5
- 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 5
- 238000002156 mixing Methods 0.000 description 5
- 229910000027 potassium carbonate Inorganic materials 0.000 description 5
- 238000001556 precipitation Methods 0.000 description 5
- 229910052717 sulfur Inorganic materials 0.000 description 5
- 239000011593 sulfur Substances 0.000 description 5
- 238000003786 synthesis reaction Methods 0.000 description 5
- 208000012868 Overgrowth Diseases 0.000 description 4
- 230000003115 biocidal effect Effects 0.000 description 4
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 4
- 229920001971 elastomer Polymers 0.000 description 4
- 239000003822 epoxy resin Substances 0.000 description 4
- 238000000227 grinding Methods 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 229920000647 polyepoxide Polymers 0.000 description 4
- 229920000915 polyvinyl chloride Polymers 0.000 description 4
- 239000004800 polyvinyl chloride Substances 0.000 description 4
- 229920005989 resin Polymers 0.000 description 4
- 239000011347 resin Substances 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- 239000000454 talc Substances 0.000 description 4
- 229910052623 talc Inorganic materials 0.000 description 4
- DYALFOTWKUYHSX-UHFFFAOYSA-N 3-(4-methylphenyl)-5-methylsulfonyl-1,2,4-thiadiazole Chemical compound C1=CC(C)=CC=C1C1=NSC(S(C)(=O)=O)=N1 DYALFOTWKUYHSX-UHFFFAOYSA-N 0.000 description 3
- QGJOPFRUJISHPQ-UHFFFAOYSA-N Carbon disulfide Chemical compound S=C=S QGJOPFRUJISHPQ-UHFFFAOYSA-N 0.000 description 3
- 239000004593 Epoxy Substances 0.000 description 3
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 3
- NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 3
- UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 3
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- IRERQBUNZFJFGC-UHFFFAOYSA-L azure blue Chemical compound [Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Al+3].[Al+3].[Al+3].[Al+3].[Al+3].[Al+3].[S-]S[S-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-] IRERQBUNZFJFGC-UHFFFAOYSA-L 0.000 description 3
- 239000003139 biocide Substances 0.000 description 3
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 3
- 125000004432 carbon atom Chemical group C* 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 229920000642 polymer Polymers 0.000 description 3
- STCOOQWBFONSKY-UHFFFAOYSA-N tributyl phosphate Chemical compound CCCCOP(=O)(OCCCC)OCCCC STCOOQWBFONSKY-UHFFFAOYSA-N 0.000 description 3
- 235000013799 ultramarine blue Nutrition 0.000 description 3
- 229920002554 vinyl polymer Polymers 0.000 description 3
- 238000010626 work up procedure Methods 0.000 description 3
- 239000011787 zinc oxide Substances 0.000 description 3
- YGTAZGSLCXNBQL-UHFFFAOYSA-N 1,2,4-thiadiazole Chemical compound C=1N=CSN=1 YGTAZGSLCXNBQL-UHFFFAOYSA-N 0.000 description 2
- BTLDOPMPDBCPPJ-UHFFFAOYSA-N 3-(4-chlorophenyl)-5-methylsulfonyl-1,2,4-thiadiazole Chemical compound S1C(S(=O)(=O)C)=NC(C=2C=CC(Cl)=CC=2)=N1 BTLDOPMPDBCPPJ-UHFFFAOYSA-N 0.000 description 2
- LVUOLMAWRDSAHJ-UHFFFAOYSA-N 5-methylsulfonyl-3-(4-nitrophenyl)-1,2,4-thiadiazole Chemical compound S1C(S(=O)(=O)C)=NC(C=2C=CC(=CC=2)[N+]([O-])=O)=N1 LVUOLMAWRDSAHJ-UHFFFAOYSA-N 0.000 description 2
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 2
- 241000195493 Cryptophyta Species 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 2
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 2
- KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 description 2
- 229920006387 Vinylite Polymers 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 2
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 2
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 2
- 229940106691 bisphenol a Drugs 0.000 description 2
- 239000001055 blue pigment Substances 0.000 description 2
- 239000000460 chlorine Substances 0.000 description 2
- 229910052801 chlorine Inorganic materials 0.000 description 2
- 239000003086 colorant Substances 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- BERDEBHAJNAUOM-UHFFFAOYSA-N copper(i) oxide Chemical compound [Cu]O[Cu] BERDEBHAJNAUOM-UHFFFAOYSA-N 0.000 description 2
- BQVVSSAWECGTRN-UHFFFAOYSA-L copper;dithiocyanate Chemical compound [Cu+2].[S-]C#N.[S-]C#N BQVVSSAWECGTRN-UHFFFAOYSA-L 0.000 description 2
- DMBHHRLKUKUOEG-UHFFFAOYSA-N diphenylamine Chemical compound C=1C=CC=CC=1NC1=CC=CC=C1 DMBHHRLKUKUOEG-UHFFFAOYSA-N 0.000 description 2
- 239000002270 dispersing agent Substances 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000012423 maintenance Methods 0.000 description 2
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 2
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 2
- RXAOGVQDNBYURA-UHFFFAOYSA-N (4-chlorobenzenecarboximidoyl)azanium;chloride Chemical compound Cl.NC(=N)C1=CC=C(Cl)C=C1 RXAOGVQDNBYURA-UHFFFAOYSA-N 0.000 description 1
- JLHMJWHSBYZWJJ-UHFFFAOYSA-N 1,2-thiazole 1-oxide Chemical class O=S1C=CC=N1 JLHMJWHSBYZWJJ-UHFFFAOYSA-N 0.000 description 1
- TUBQDCKAWGHZPF-UHFFFAOYSA-N 1,3-benzothiazol-2-ylsulfanylmethyl thiocyanate Chemical compound C1=CC=C2SC(SCSC#N)=NC2=C1 TUBQDCKAWGHZPF-UHFFFAOYSA-N 0.000 description 1
- VILCJCGEZXAXTO-UHFFFAOYSA-N 2,2,2-tetramine Chemical compound NCCNCCNCCN VILCJCGEZXAXTO-UHFFFAOYSA-N 0.000 description 1
- FJWGRXKOBIVTFA-UHFFFAOYSA-N 2,3-dibromobutanedioic acid Chemical class OC(=O)C(Br)C(Br)C(O)=O FJWGRXKOBIVTFA-UHFFFAOYSA-N 0.000 description 1
- CIPUZYQYFMMYAF-UHFFFAOYSA-N 2,4-dichlorobenzenecarboximidamide;hydrochloride Chemical compound [Cl-].NC(=[NH2+])C1=CC=C(Cl)C=C1Cl CIPUZYQYFMMYAF-UHFFFAOYSA-N 0.000 description 1
- YAUCKEPYKXHCFF-UHFFFAOYSA-N 2-carbamothioylsulfanylethyl carbamodithioate;manganese Chemical class [Mn].NC(=S)SCCSC(N)=S YAUCKEPYKXHCFF-UHFFFAOYSA-N 0.000 description 1
- 125000004189 3,4-dichlorophenyl group Chemical group [H]C1=C([H])C(Cl)=C(Cl)C([H])=C1* 0.000 description 1
- LPXGTFJQONCRKV-UHFFFAOYSA-N 3-(4-chlorophenyl)-5-methylsulfanyl-1,2,4-thiadiazole Chemical compound S1C(SC)=NC(C=2C=CC(Cl)=CC=2)=N1 LPXGTFJQONCRKV-UHFFFAOYSA-N 0.000 description 1
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- 229940099451 3-iodo-2-propynylbutylcarbamate Drugs 0.000 description 1
- WYVVKGNFXHOCQV-UHFFFAOYSA-N 3-iodoprop-2-yn-1-yl butylcarbamate Chemical compound CCCCNC(=O)OCC#CI WYVVKGNFXHOCQV-UHFFFAOYSA-N 0.000 description 1
- PAPIULIUHITHDW-UHFFFAOYSA-N 3-phenyl-1,2,4-thiadiazole Chemical compound S1C=NC(C=2C=CC=CC=2)=N1 PAPIULIUHITHDW-UHFFFAOYSA-N 0.000 description 1
- SIXWIUJQBBANGK-UHFFFAOYSA-N 4-(4-fluorophenyl)-1h-pyrazol-5-amine Chemical compound N1N=CC(C=2C=CC(F)=CC=2)=C1N SIXWIUJQBBANGK-UHFFFAOYSA-N 0.000 description 1
- PDOCXVITMZPJEH-UHFFFAOYSA-N 5-methylsulfanyl-3-(4-nitrophenyl)-1,2,4-thiadiazole Chemical compound S1C(SC)=NC(C=2C=CC(=CC=2)[N+]([O-])=O)=N1 PDOCXVITMZPJEH-UHFFFAOYSA-N 0.000 description 1
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- 239000010936 titanium Substances 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- LPUCKLOWOWADAC-UHFFFAOYSA-M tributylstannyl 2-methylprop-2-enoate Chemical compound CCCC[Sn](CCCC)(CCCC)OC(=O)C(C)=C LPUCKLOWOWADAC-UHFFFAOYSA-M 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 229940043810 zinc pyrithione Drugs 0.000 description 1
- PICXIOQBANWBIZ-UHFFFAOYSA-N zinc;1-oxidopyridine-2-thione Chemical compound [Zn+2].[O-]N1C=CC=CC1=S.[O-]N1C=CC=CC1=S PICXIOQBANWBIZ-UHFFFAOYSA-N 0.000 description 1
- DUBNHZYBDBBJHD-UHFFFAOYSA-L ziram Chemical compound [Zn+2].CN(C)C([S-])=S.CN(C)C([S-])=S DUBNHZYBDBBJHD-UHFFFAOYSA-L 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D5/00—Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
- C09D5/16—Antifouling paints; Underwater paints
- C09D5/1606—Antifouling paints; Underwater paints characterised by the anti-fouling agent
- C09D5/1612—Non-macromolecular compounds
- C09D5/1625—Non-macromolecular compounds organic
-
- 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
- A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
- A01N43/82—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms five-membered rings with three ring hetero atoms
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Wood Science & Technology (AREA)
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Plant Pathology (AREA)
- General Health & Medical Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Pest Control & Pesticides (AREA)
- Materials Engineering (AREA)
- Health & Medical Sciences (AREA)
- Dentistry (AREA)
- Organic Chemistry (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Paints Or Removers (AREA)
- Lubricants (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen- Or Sulfur-Containing Heterocyclic Ring Compounds With Rings Of Six Or More Members (AREA)
Priority Applications (13)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE4230955A DE4230955A1 (de) | 1992-09-16 | 1992-09-16 | Verwendung von Thiadiazol-Verbindungen als Antifouling-Wirkstoff |
| DE59303733T DE59303733D1 (de) | 1992-09-16 | 1993-07-10 | Verwendung von Thiadiazol-Verbindungen als Antifouling-Wirkstoff |
| ES93111095T ES2093328T3 (es) | 1992-09-16 | 1993-07-10 | Utilizacion de compuestos de tiadiazol como sustancia activa antiensuciamiento. |
| DK93111095.1T DK0588007T3 (US06252093-20010626-C00008.png) | 1992-09-16 | 1993-07-10 | |
| EP93111095A EP0588007B1 (de) | 1992-09-16 | 1993-07-10 | Verwendung von Thiadiazol-Verbindungen als Antifouling-Wirkstoff |
| JP5228678A JPH06211609A (ja) | 1992-09-16 | 1993-09-14 | 防汚作用物質及び該物質を含有する防汚製剤 |
| CA002106287A CA2106287C (en) | 1992-09-16 | 1993-09-15 | Use of thiadiazole compounds as an antifouling active ingredient |
| NO933286A NO303861B1 (no) | 1992-09-16 | 1993-09-15 | Anvendelse og preparat av tiadiazolforbindelser som grohemmende aktivt materiale i marine miljöer |
| US08/123,185 US5332430A (en) | 1992-09-16 | 1993-09-15 | Use of thiadiazole compounds as an antifouling active ingredient |
| AU47400/93A AU666763B2 (en) | 1992-09-16 | 1993-09-16 | Use of thiadiazole compounds as an antifouling active ingredient |
| FI934064A FI934064A (fi) | 1992-09-16 | 1993-09-16 | Anvaendning av tiadiazolfoereningar som aktivt aemne foer foerebyggande av bottenvaextlighet hos fartyg |
| MX9305705A MX9305705A (es) | 1992-09-16 | 1993-09-17 | Utilizacion de compuestos de tiadiazol como agenteanti-descomposicion. |
| GR960402619T GR3021267T3 (en) | 1992-09-16 | 1996-10-04 | Use of thiadiazoles as antifouling agent. |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE4230955A DE4230955A1 (de) | 1992-09-16 | 1992-09-16 | Verwendung von Thiadiazol-Verbindungen als Antifouling-Wirkstoff |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE4230955A1 true DE4230955A1 (de) | 1994-03-17 |
Family
ID=6468078
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE4230955A Withdrawn DE4230955A1 (de) | 1992-09-16 | 1992-09-16 | Verwendung von Thiadiazol-Verbindungen als Antifouling-Wirkstoff |
| DE59303733T Expired - Lifetime DE59303733D1 (de) | 1992-09-16 | 1993-07-10 | Verwendung von Thiadiazol-Verbindungen als Antifouling-Wirkstoff |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE59303733T Expired - Lifetime DE59303733D1 (de) | 1992-09-16 | 1993-07-10 | Verwendung von Thiadiazol-Verbindungen als Antifouling-Wirkstoff |
Country Status (12)
Families Citing this family (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5472993A (en) * | 1994-12-30 | 1995-12-05 | Korea Chemical Co., Ltd. | Anti-fouling paint |
| NO952270D0 (no) * | 1995-06-08 | 1995-06-08 | Jotun As | Polymerer for grohemmende maling og fremgangsmåte for fremstilling derav |
| EP0841353A1 (de) | 1996-11-07 | 1998-05-13 | Witco GmbH | Verfahren zur Herstellung von polymeren Bindemitteln und deren Verwendung für Antifouling-Anstrichsysteme |
| EP0841380B1 (de) * | 1996-11-07 | 1999-08-25 | Witco GmbH | Verfahren zur Herstellung von polymeren Bindemitteln und deren Verwendung für Antifouling-Anstrichsysteme |
| DE10209934A1 (de) * | 2002-03-07 | 2003-10-02 | Beta Tec Hopfenprodukte Gmbh | Verfahren zur Kontrolle von biologischen Prozessen in Wasser |
| DE60305844T2 (de) * | 2002-11-22 | 2007-05-16 | Rohm And Haas Co. | Wässrige Dispersion von organischen Feststoffen mit niedrigem Schmelzpunkt |
| DE102005011990A1 (de) * | 2005-03-14 | 2006-09-21 | Basf Ag | Foulingresistente Polyurethane, insbesondere für maritime Anwendungen |
| JP5360759B2 (ja) * | 2009-06-08 | 2013-12-04 | 日東化成株式会社 | 防汚塗料組成物、該組成物を用いて形成される防汚塗膜、該塗膜を表面に有する塗装物、および該塗膜を形成する防汚処理方法 |
| EP3039103A4 (en) * | 2013-08-31 | 2017-06-14 | Houghton Technical Corp. | Hydraulic fluid compositions |
| CN107531895A (zh) | 2015-04-15 | 2018-01-02 | 好富顿技术股份有限公司 | 使用聚酰胺多胺和非聚合酰胺胺的组合物和方法 |
Family Cites Families (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA588046A (en) * | 1959-12-01 | S. Karsten Kenneth | Wax compositions containing a mercaptobenzothiazole as a microbicide | |
| US3597426A (en) * | 1968-10-02 | 1971-08-03 | M & T Chemicals Inc | Unsymmetrical disubstituted perthiocyanates |
| GB1356391A (en) * | 1970-09-09 | 1974-06-12 | Fisons Ltd | Pesticides |
| DE2242187A1 (de) * | 1971-08-31 | 1973-03-08 | Ciba Geigy Ag | Heterocyclische verbindungen |
| CH550538A (de) * | 1971-08-31 | 1974-06-28 | Ciba Geigy Ag | Handelsfaehiges mittel zur bekaempfung von schaedlichen mikroorganismen. |
| AR207229A1 (es) * | 1973-08-20 | 1976-09-22 | Rohm & Haas | Composicion de recubrimiento estabilizada con formaldehido y metodo para su preparacion |
| JPS519705A (ja) * | 1974-07-15 | 1976-01-26 | Taiyo Kagaku Kogyo Co Ltd | Mokuzainobokabiho |
| US4209522A (en) * | 1978-06-28 | 1980-06-24 | The Dow Chemical Company | Antimicrobial bis(5-nitro-2-thiazolyl)thioisothiazoles and thiadiazoles |
| US4711915A (en) * | 1986-04-07 | 1987-12-08 | R. T. Vanderbilt Company, Inc. | Surface coating compositions containing substituted 1,3,4-thiadiazoles |
| DE3722320A1 (de) * | 1987-07-07 | 1989-01-19 | Bayer Ag | Mikrobizide mittel |
| JPH02173165A (ja) * | 1988-12-27 | 1990-07-04 | Nippon Soda Co Ltd | 防汚剤 |
| DE4131138A1 (de) * | 1991-09-19 | 1993-03-25 | Bayer Ag | 3-(4-bromphenyl)-5-methylsulfonyl-1,2,4- thiadiazol,ein verfahren zur herstellung, seine verwendung und neue zwischenprodukte |
-
1992
- 1992-09-16 DE DE4230955A patent/DE4230955A1/de not_active Withdrawn
-
1993
- 1993-07-10 ES ES93111095T patent/ES2093328T3/es not_active Expired - Lifetime
- 1993-07-10 DE DE59303733T patent/DE59303733D1/de not_active Expired - Lifetime
- 1993-07-10 EP EP93111095A patent/EP0588007B1/de not_active Expired - Lifetime
- 1993-07-10 DK DK93111095.1T patent/DK0588007T3/da active
- 1993-09-14 JP JP5228678A patent/JPH06211609A/ja active Pending
- 1993-09-15 US US08/123,185 patent/US5332430A/en not_active Expired - Fee Related
- 1993-09-15 CA CA002106287A patent/CA2106287C/en not_active Expired - Fee Related
- 1993-09-15 NO NO933286A patent/NO303861B1/no unknown
- 1993-09-16 AU AU47400/93A patent/AU666763B2/en not_active Ceased
- 1993-09-16 FI FI934064A patent/FI934064A/fi unknown
- 1993-09-17 MX MX9305705A patent/MX9305705A/es not_active IP Right Cessation
-
1996
- 1996-10-04 GR GR960402619T patent/GR3021267T3/el unknown
Also Published As
| Publication number | Publication date |
|---|---|
| JPH06211609A (ja) | 1994-08-02 |
| AU666763B2 (en) | 1996-02-22 |
| GR3021267T3 (en) | 1997-01-31 |
| NO303861B1 (no) | 1998-09-14 |
| EP0588007B1 (de) | 1996-09-11 |
| MX9305705A (es) | 1994-05-31 |
| NO933286L (no) | 1994-03-17 |
| ES2093328T3 (es) | 1996-12-16 |
| US5332430A (en) | 1994-07-26 |
| CA2106287A1 (en) | 1994-03-17 |
| NO933286D0 (no) | 1993-09-15 |
| FI934064A0 (fi) | 1993-09-16 |
| DK0588007T3 (US06252093-20010626-C00008.png) | 1997-02-24 |
| FI934064A (fi) | 1994-03-17 |
| DE59303733D1 (de) | 1996-10-17 |
| AU4740093A (en) | 1994-03-24 |
| EP0588007A1 (de) | 1994-03-23 |
| CA2106287C (en) | 1997-07-01 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| 8130 | Withdrawal |