CZ292552B6 - Použití aminoizothiazolů jako mikrobicidů - Google Patents
Použití aminoizothiazolů jako mikrobicidů Download PDFInfo
- Publication number
- CZ292552B6 CZ292552B6 CZ19992263A CZ226399A CZ292552B6 CZ 292552 B6 CZ292552 B6 CZ 292552B6 CZ 19992263 A CZ19992263 A CZ 19992263A CZ 226399 A CZ226399 A CZ 226399A CZ 292552 B6 CZ292552 B6 CZ 292552B6
- Authority
- CZ
- Czechia
- Prior art keywords
- methyl
- formula
- microorganisms
- aminoisothiazoles
- weight
- Prior art date
Links
- 230000003641 microbiacidal effect Effects 0.000 title claims abstract description 13
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- 229940124561 microbicide Drugs 0.000 title claims abstract description 9
- 244000005700 microbiome Species 0.000 claims abstract description 17
- 239000002253 acid Substances 0.000 claims abstract description 12
- 150000003839 salts Chemical class 0.000 claims abstract description 7
- 238000000034 method Methods 0.000 claims abstract description 5
- 229910052751 metal Inorganic materials 0.000 claims abstract description 4
- 239000002184 metal Substances 0.000 claims abstract description 4
- 125000005843 halogen group Chemical group 0.000 claims abstract description 3
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- 239000000463 material Substances 0.000 claims description 17
- 239000000203 mixture Substances 0.000 claims description 12
- 238000002360 preparation method Methods 0.000 claims description 11
- SQVCWDJYTNCVBH-UHFFFAOYSA-N (5-amino-3-methyl-1,2-thiazol-4-yl) thiocyanate Chemical compound CC1=NSC(N)=C1SC#N SQVCWDJYTNCVBH-UHFFFAOYSA-N 0.000 claims description 7
- 230000006378 damage Effects 0.000 claims description 6
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 5
- 229910052739 hydrogen Inorganic materials 0.000 claims description 2
- 239000001257 hydrogen Substances 0.000 claims description 2
- 238000002156 mixing Methods 0.000 claims description 2
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- 239000012876 carrier material Substances 0.000 claims 1
- 125000000858 thiocyanato group Chemical group *SC#N 0.000 claims 1
- 150000007513 acids Chemical class 0.000 abstract description 8
- 125000000217 alkyl group Chemical group 0.000 abstract description 3
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- YXIWHUQXZSMYRE-UHFFFAOYSA-N 1,3-benzothiazole-2-thiol Chemical compound C1=CC=C2SC(S)=NC2=C1 YXIWHUQXZSMYRE-UHFFFAOYSA-N 0.000 description 2
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- 239000005916 Methomyl Substances 0.000 description 2
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- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 2
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 2
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- ATROHALUCMTWTB-OWBHPGMISA-N phoxim Chemical compound CCOP(=S)(OCC)O\N=C(\C#N)C1=CC=CC=C1 ATROHALUCMTWTB-OWBHPGMISA-N 0.000 description 1
- 229950001664 phoxim Drugs 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- YFGYUFNIOHWBOB-UHFFFAOYSA-N pirimicarb Chemical compound CN(C)C(=O)OC1=NC(N(C)C)=NC(C)=C1C YFGYUFNIOHWBOB-UHFFFAOYSA-N 0.000 description 1
- 239000002798 polar solvent Substances 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 239000002243 precursor Substances 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- WHHIPMZEDGBUCC-UHFFFAOYSA-N probenazole Chemical compound C1=CC=C2C(OCC=C)=NS(=O)(=O)C2=C1 WHHIPMZEDGBUCC-UHFFFAOYSA-N 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- QYMMJNLHFKGANY-UHFFFAOYSA-N profenofos Chemical compound CCCSP(=O)(OCC)OC1=CC=C(Br)C=C1Cl QYMMJNLHFKGANY-UHFFFAOYSA-N 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- PWYIUEFFPNVCMW-UHFFFAOYSA-N propaphos Chemical compound CCCOP(=O)(OCCC)OC1=CC=C(SC)C=C1 PWYIUEFFPNVCMW-UHFFFAOYSA-N 0.000 description 1
- 235000019260 propionic acid Nutrition 0.000 description 1
- RUOJZAUFBMNUDX-UHFFFAOYSA-N propylene carbonate Chemical compound CC1COC(=O)O1 RUOJZAUFBMNUDX-UHFFFAOYSA-N 0.000 description 1
- 229940007042 proteus vulgaris Drugs 0.000 description 1
- QHMTXANCGGJZRX-WUXMJOGZSA-N pymetrozine Chemical compound C1C(C)=NNC(=O)N1\N=C\C1=CC=CN=C1 QHMTXANCGGJZRX-WUXMJOGZSA-N 0.000 description 1
- QHGVXILFMXYDRS-UHFFFAOYSA-N pyraclofos Chemical compound C1=C(OP(=O)(OCC)SCCC)C=NN1C1=CC=C(Cl)C=C1 QHGVXILFMXYDRS-UHFFFAOYSA-N 0.000 description 1
- 229940015367 pyrethrum Drugs 0.000 description 1
- DWFZBUWUXWZWKD-UHFFFAOYSA-N pyridaben Chemical compound C1=CC(C(C)(C)C)=CC=C1CSC1=C(Cl)C(=O)N(C(C)(C)C)N=C1 DWFZBUWUXWZWKD-UHFFFAOYSA-N 0.000 description 1
- ZLIBICFPKPWGIZ-UHFFFAOYSA-N pyrimethanil Chemical compound CC1=CC(C)=NC(NC=2C=CC=CC=2)=N1 ZLIBICFPKPWGIZ-UHFFFAOYSA-N 0.000 description 1
- ITKAIUGKVKDENI-UHFFFAOYSA-N pyrimidifen Chemical compound CC1=C(C)C(CCOCC)=CC=C1OCCNC1=NC=NC(CC)=C1Cl ITKAIUGKVKDENI-UHFFFAOYSA-N 0.000 description 1
- NHDHVHZZCFYRSB-UHFFFAOYSA-N pyriproxyfen Chemical compound C=1C=CC=NC=1OC(C)COC(C=C1)=CC=C1OC1=CC=CC=C1 NHDHVHZZCFYRSB-UHFFFAOYSA-N 0.000 description 1
- JYQUHIFYBATCCY-UHFFFAOYSA-N quinalphos Chemical compound C1=CC=CC2=NC(OP(=S)(OCC)OCC)=CN=C21 JYQUHIFYBATCCY-UHFFFAOYSA-N 0.000 description 1
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
- MCJGNVYPOGVAJF-UHFFFAOYSA-N quinolin-8-ol Chemical compound C1=CN=C2C(O)=CC=CC2=C1 MCJGNVYPOGVAJF-UHFFFAOYSA-N 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 238000005057 refrigeration Methods 0.000 description 1
- HPYNBECUCCGGPA-UHFFFAOYSA-N silafluofen Chemical compound C1=CC(OCC)=CC=C1[Si](C)(C)CCCC1=CC=C(F)C(OC=2C=CC=CC=2)=C1 HPYNBECUCCGGPA-UHFFFAOYSA-N 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 239000010802 sludge Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000011550 stock solution Substances 0.000 description 1
- 229960005322 streptomycin Drugs 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- XIUROWKZWPIAIB-UHFFFAOYSA-N sulfotep Chemical compound CCOP(=S)(OCC)OP(=S)(OCC)OCC XIUROWKZWPIAIB-UHFFFAOYSA-N 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- JXHJNEJVUNHLKO-UHFFFAOYSA-N sulprofos Chemical compound CCCSP(=S)(OCC)OC1=CC=C(SC)C=C1 JXHJNEJVUNHLKO-UHFFFAOYSA-N 0.000 description 1
- 230000002195 synergetic effect Effects 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- QYPNKSZPJQQLRK-UHFFFAOYSA-N tebufenozide Chemical compound C1=CC(CC)=CC=C1C(=O)NN(C(C)(C)C)C(=O)C1=CC(C)=CC(C)=C1 QYPNKSZPJQQLRK-UHFFFAOYSA-N 0.000 description 1
- AWYOMXWDGWUJHS-UHFFFAOYSA-N tebupirimfos Chemical compound CCOP(=S)(OC(C)C)OC1=CN=C(C(C)(C)C)N=C1 AWYOMXWDGWUJHS-UHFFFAOYSA-N 0.000 description 1
- ROZUQUDEWZIBHV-UHFFFAOYSA-N tecloftalam Chemical compound OC(=O)C1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1C(=O)NC1=CC=CC(Cl)=C1Cl ROZUQUDEWZIBHV-UHFFFAOYSA-N 0.000 description 1
- CJDWRQLODFKPEL-UHFFFAOYSA-N teflubenzuron Chemical compound FC1=CC=CC(F)=C1C(=O)NC(=O)NC1=CC(Cl)=C(F)C(Cl)=C1F CJDWRQLODFKPEL-UHFFFAOYSA-N 0.000 description 1
- WWJZWCUNLNYYAU-UHFFFAOYSA-N temephos Chemical compound C1=CC(OP(=S)(OC)OC)=CC=C1SC1=CC=C(OP(=S)(OC)OC)C=C1 WWJZWCUNLNYYAU-UHFFFAOYSA-N 0.000 description 1
- IWVCMVBTMGNXQD-UHFFFAOYSA-N terramycin dehydrate Natural products C1=CC=C2C(O)(C)C3C(O)C4C(N(C)C)C(O)=C(C(N)=O)C(=O)C4(O)C(O)=C3C(=O)C2=C1O IWVCMVBTMGNXQD-UHFFFAOYSA-N 0.000 description 1
- UBCKGWBNUIFUST-YHYXMXQVSA-N tetrachlorvinphos Chemical compound COP(=O)(OC)O\C(=C/Cl)C1=CC(Cl)=C(Cl)C=C1Cl UBCKGWBNUIFUST-YHYXMXQVSA-N 0.000 description 1
- CXWXQJXEFPUFDZ-UHFFFAOYSA-N tetralin Chemical compound C1=CC=C2CCCCC2=C1 CXWXQJXEFPUFDZ-UHFFFAOYSA-N 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
- 150000003567 thiocyanates Chemical class 0.000 description 1
- BAKXBZPQTXCKRR-UHFFFAOYSA-N thiodicarb Chemical compound CSC(C)=NOC(=O)NSNC(=O)ON=C(C)SC BAKXBZPQTXCKRR-UHFFFAOYSA-N 0.000 description 1
- QGHREAKMXXNCOA-UHFFFAOYSA-N thiophanate-methyl Chemical compound COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC QGHREAKMXXNCOA-UHFFFAOYSA-N 0.000 description 1
- NKNFWVNSBIXGLL-UHFFFAOYSA-N triazamate Chemical compound CCOC(=O)CSC1=NC(C(C)(C)C)=NN1C(=O)N(C)C NKNFWVNSBIXGLL-UHFFFAOYSA-N 0.000 description 1
- AMFGTOFWMRQMEM-UHFFFAOYSA-N triazophos Chemical compound N1=C(OP(=S)(OCC)OCC)N=CN1C1=CC=CC=C1 AMFGTOFWMRQMEM-UHFFFAOYSA-N 0.000 description 1
- ZSMRBQSZBQBLKB-UHFFFAOYSA-M tributylstannyl 2-hydroxybenzoate Chemical compound CCCC[Sn](CCCC)(CCCC)OC(=O)C1=CC=CC=C1O ZSMRBQSZBQBLKB-UHFFFAOYSA-M 0.000 description 1
- JUEAPPHORMOWPK-UHFFFAOYSA-M tributylstannyl benzoate Chemical compound CCCC[Sn](CCCC)(CCCC)OC(=O)C1=CC=CC=C1 JUEAPPHORMOWPK-UHFFFAOYSA-M 0.000 description 1
- PIILXFBHQILWPS-UHFFFAOYSA-N tributyltin Chemical compound CCCC[Sn](CCCC)CCCC PIILXFBHQILWPS-UHFFFAOYSA-N 0.000 description 1
- CEYYIKYYFSTQRU-UHFFFAOYSA-M trimethyl(tetradecyl)azanium;chloride Chemical compound [Cl-].CCCCCCCCCCCCCC[N+](C)(C)C CEYYIKYYFSTQRU-UHFFFAOYSA-M 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 239000008096 xylene Substances 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
-
- 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
- A01N43/80—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 one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,2
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)
- Thiazole And Isothizaole Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Použití aminoizothiazolů obecného vzorce I, kde R je atom vodíku nebo alkylová skupina s 1 až 4 atomy uhlíku a X je atom halogenu, NO.sub.2.n., CN nebo SCN, jejich komplexů s kovy a jejich solí s kyselinami jako mikrobicidů pro ochranu technických materiálů před napadením a zničením mikroorganismy. Způsob ochrany technických materiálů před napadením a zničením mikroorganismy a způsob přípravy mikrobicidních prostředků.ŕ
Description
Použití aminoizothiazolů jako mikrobicidů
Oblast techniky
Vynález se týká použití aminoizothiazolů jako mikrobicidů pro ochranu technických materiálů před napadením a zničením mikroorganismy. Dále se vynález týká způsobu ochrany technických materiálů před napadením a zničením mikroorganismy.
Dosavadní stav techniky
Je známo, že izothiazoly (US 3 761 488, US 4 105 431, US 4 252 694, US 4 265 899, US 4 279 762, US 5 430 046 a EP 697 409) a deriváty benzothiofenu (DE44 11 912) a také směsi určitých derivátů azolu samoniovými sloučeninami (EP 533 016), mají mikrobicidní vlastnosti. Příprava některých z těchto sloučenin je velmi komplikovaná a jejich účinnost, zejména při nízkých aplikačních dávkách, není vždy dostatečná.
Byly popsány 5-aminoizothiazoly jako kopulační komponenty u azobarviv (EP 362 708, EP315 898). O 5-aminoizothiazolech (v mnoha případech N-acylovaných) je také známo, že mají herbicidní (EP 640 597, DE 24 34 922, DE 22 49 162, FR 2 132 691, US 4 032 321, US 4 032 322, ZA 7 202 352), baktericidní a protivirovou účinnost (L. Kuczynski aj., Pol., J. Pharmacol. Pharm. (1984), 36 (5), 485 až 491), a jsou použitelné jako meziprodukty pro léčiva a činidla pro ochranu plodin.
Je proto cílem předloženého vynálezu poskytnout sloučeniny, které mohou být použity jako mikrobicidy pro ochranu materiálů a které jsou snadno dostupné a mají dobrou mikrobicidní účinnost.
Podstata vynálezu
Bylo nyní zjištěno, že se 5-aminoizothiazoly obecného vzorce I
R X
kde
R je atom vodíku nebo alkylová skupina s 1 až 4 atomy uhlíku a
X je atom halogenu, NO2, CN nebo SCN, a jejich komplexy s kovy a jejich soli s kyselinami, dají velmi dobře použít jako mikrobicidy při ochraně materiálů. Výhodnými jsou sloučeniny, kde R je alkylová skupina s 1 až 4 atomy uhlíku, zejména methylová skupina. Dále jsou výhodnými sloučeniny, kde X je CN a zejména SCN.
Při obzvláště výhodném provedení se použije 3-methyl-4-thiokyanato-5-aminoizothiazol vzorce Ic
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a jeho komplexy s kovy a jeho soli s kyselinami.
Sloučeniny obecného vzorce I pro použiti podle vynálezu se připravují sledem reakcí známým z EP-A 640 597 převedením izothiazolů obecného vzorce II
pomocí halogenačního činidla na halogenovanou sloučeninu obecného vzorce la, kde Hal je F, Cl, Br nebo I, která se potom v případě potřeby převede na sloučeninu obecného vzorce Ib, kde X' je SCN nebo CN reakcí s thiokyanáty nebo kyanidy. Příprava izothiazolů obecného vzorce II je popsána například v DE 17 70 819. Příprava 3-methyl-5-aminoizothiazolu je popsána v práci A. Adams aj., J. Chem. Soc. 1959, str. 3061.
Aminoizothiazoly obecného vzorce I, jako takové nebo ve formě přípravku, jsou vhodné pro ochranu technických materiálů před napadením a zničením mikroorganismy.
Technickými materiály se míní neživé materiály získané technickými a průmyslovými postupy nebo neživé materiály zamýšlené pro použití v průmyslu. Technickými materiály, které mají být chráněny účinnými sloučeninami obecného vzorce I před změnou nebo zničením mikroby, jsou například disperze, lepidla, klihy, kosmetika, roztoky škrobu, voskové emulze, emulze hlinek, papír, šlichty, apretury, srážecí lázně, textilie, kůže, surové kůže, želatinové přípravky, okenné tmely, těsnicí tmely, dřevo, nátěrové hmoty, plastické hmoty, chladicí a mazací prostředky, vrtací oleje a další materiály, které mohou být napadeny nebo zničeny mikroorganismy. Tyto sloučeniny jsou dále vhodné jak prostředky proti slizu v papírenském průmyslu, chladírenství ave zvlhčovačích ovzduší. Aminoizothiazoly obecného vzorce I se zejména výhodně používají u disperzí, jako jsou polymemí disperze a nátěrové hmot}'.
Mikroorganismy, které způsobují rozklad nebo změnu technických materiálů, jsou například spory, viry, bakterie, plísně, kvasinky, řasy a kalové organismy. Účinné sloučeniny nebo přípravky podle vynálezu s výhodou působí proti plísním, bakteriím a řasám.
Jako příklady mikroorganismů lze uvést následující druhy: Altemaria altemata, Altemaria tenuis, Aspergillus niger, Aureobasidium pullulans, Candida albicans, Chaetomium globosum, Citrobacter freundii, Cladosporium resinae, Coniophora puteana, Desulfovibrio desulfuricans, Escherichia coli, Klebsiella pneumoniae, Lentinus tigrinus, Penicillium expansum, Penicillium funiculosum, Penicillium glaucum, Polysporus versicolor, Próteus mirabilis, Próteus vulgaris, Pseudomonas aeruginosa, Sclerophoma pityophila, Saccaromyces cerevisiae, Staphylococcus aureus, Streptoverticillium rubrireticuli, Trichoderma viride.
V závislosti na jejich fyzikálních a chemických vlastnostech a na požadované aplikaci lze účinné sloučeniny obecného vzorce I převést do formy běžných přípravků, například roztoků, emulzí, prášků, past nebo disperzí.
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Tyto přípravky s účinnou látkou se připravují obvyklým způsobem, například míšením účinných sloučenin s vhodnými plnivy nebo rozpouštědly, přičemž v případě potřeby lze též použít povrchově aktivní činidla, to je emulgátory nebo dispergační činidla. Použije-li se voda, organická rozpouštědla se obecně používají jako pomocná rozpouštědla. Vhodnými rozpouštědly 5 jsou například alkoholy, jako je methanol, ethanol, propanol, butanol a cyklohexanol, nebo glykoly, jako je propylenglykol, 2-fenoxyethanol, fenoxypropanol, nebo alifatické, cyklické a aromatické uhlovodíky, jako je toluen, xylen, mesitylen, parafín, tetrahydronaftalen, alkylované naftaleny nebo jejich deriváty, chlorbenzen, dichlorbenzen nebo silně polární rozpouštědla, jako je Ν,Ν-dimethylformamid, Ν,Ν-dimethylacetamid, dimethylsulfoxid nebo N-methylpyrrolidon.
Vhodnými emulgátory jsou například soli s alkalickými kovy, s kovy alkalických zemin nebo amoniové soli aromatických sulfonových kyselin, například lignosulfonové kyseliny, fenolsulfonové kyseliny, naftalensulfonové kyseliny a dibutylnaftalensulfonové kyseliny, a mastných kyselin, alkylsulfonáty a sulfáty mastných alkoholů a soli sulfatovaných hexadekanolů, hepta15 dekanolů a oktadekanolů, a kondenzační produkty sulfonovaných naftalenů nebo derivátů naftalenu s formaldehydem, kondenzační produkty naftalenů nebo naftalensulfonových kyselin t s fenolem a formaldehydem, ethery polyoxyethylenovaných mastných alkoholů, ethery polyoxyethylenovaného oktylfenolu, ethoxylovaný izooktylfenol, alkylfenylpolyglykolethery, tributylfenylpolyglykolethery, izotridecylalkohol, alkylarylpolyglykolethery, ethoxylovaný ricinový olej, 20 polyoxyethylenalkylethery nebo polyoxypropylen, polyglykoletheracetát larylalkoholu, estery sorbitolu a vhodnými dispergačními činidly jsou například lignosulfítové odpadní louhy a methylcelulóza.
Pro zlepšení homogenity těchto koncentrátů lze přidávat alifatické karboxylové kyseliny. Jako 25 tyto kyseliny lze uvést například kyselinu propionovou, kyselinu hexanovou, kyselinu heptanovou, rozvětvené karboxylové kyseliny, jako je kyselina 2-ethylenhexanová, kyselina izooktanová, neokarboxylové kyseliny, alifatické dikarboxylové kyseliny, jako je kyselina sebaková, cykloalkylkarboxylové kyseliny, jako je kyselina cyklohexanová, arylkarboxylové kyseliny, jako je kyselina benzoová, kyselina 3-hydroxybenzoová nebo kyselina 4-hydroxy30 benzoová.
Nátěrovými hmotami nebo prekurzory pro přípravu nátěrových hmot mohou být disperze plastických hmot, disperze nátěrových hmot pro průmysl nátěrových hmot, roztoky škrobu, suspenze jiných surovin, jako jsou barevné pigmenty nebo barviva nebo suspenze plniv, jako je 35 kaolin, uhličitan vápenatý, kyseliny křemičité, silikagely, silikáty, talek, vápenec, křída, zemitý jíl, spraš, hlinka, dolomit, diatomická hlinka, síran vápenatý a síran hořečnatý, oxid hořečnatý nebo rozemleté plastické hmoty.
Účinnost a spektrum účinnosti účinných sloučenin obecného vzorce I nebo prostředků, 40 meziproduktů nebo přípravků, z nich připravitelných, lze zvýšit přidáním dalších, popřípadě antimikrobiálně účinných sloučenin, baktericidů, fungicidů, herbicidů, insekticidů nebo jiných účinných sloučenin pro rozšíření spektra účinnosti nebo pro získání speciálních účinků. V mnoha případech to vede k synergickému účinku, to je spektrum účinnosti směsi je vyšší než účinnost jednotlivých složek.
Zejména výhodnými dalšími složkami jsou například:
mikrobicidy:
2-(thiokyanatomethylthio)benzothiazol, l-[2-(2,4-dichlorfenyl)-2-(2-propenyloxy)ethyl]-lHimidazol, 2,4,5,6-tetrachlorizoftalodinitril, methylenbisthiokyanát, tributylcínoxid, tributylcínaftenát, tributylcínbenzoát, tributylcínsalicylát, merkaptobenzothiazol, 1,2-benzizothiazolon a jeho soli s alkalickými kovy, sloučeniny N'-hydroxy-N-cyklohexyldiazeniumoxidu s alkalickými kovy, 2-(methoxykarbonylamino)benzimidazol, 2-methyl-3-oxo-5-chlor-thiazolin-3-on, trihydroxymethylnitromethan, glutaraldehyd, chloracetamid, polyhexamethylenbisguanidy, 5-3CZ 292552 B6 chlor-2-methyl-4-izothiazolin-3-on + horečnaté soli, 2-methyl-4-izothiazolin-3-on, oxazolidiny, bizoxazolidiny, 5-dihydro-2,5-dialkoxy-2,5-dialkylfurany, diethyldodecylblenzylamoniumchlorid, dimethyloktadecyldimethylbenzylamoniumchorid, dimethyldidecylamoniumchlorid, dimethyldidodecylamoniumchlorid, trimethyltetradecylamoniumchlorid, benzyldi5 methylalkyl-(Ci2-Ci8)-amoniurnchlorid, dichlorbenzyldimethyldodecylamoniumchlorid, cetylpyridiniumchlorid, cetylpyridiniumbromid, cetyltrimethylamoniumchlorid, laurylpyridiniumchlorid, laurylpyridiniumbisulfát, benzyldodecyldi(p-oxyethyl)amoniumchlorid, dodecylbenzyltrimethylamoniumchorid, n-alkyldimethylbenzylamoniumchlorid (kde alkylový zbytek má 40 % Cn, 50 % C16), lauryldimethylethylamoniumethylsuifát, n-alkyldimethyl(l-nafrylmethy)10 amoniumchlorid (kde alkylový zbytek má 98 % Ci2, 2 % Cu), cetyldimethylbenzylamoniumchlorid, lauryldimethylbenzylamoniumchlorid, baktericidy:
bronopol, dichlorophen, nitrapyrin, dimethyldithiokarbamát, nikelnatý, kasugamycin, octhilinon, furankarboxylová kyselina, oxytetracyklin, probenazol, streptomycin, tecloftalam, síran mědi a další přípravky s mědí, fungicidy:
síra, dithiokarbamáty a jejich deriváty, jako je dimethyldithiokarbamát železitý, dimethyldithiokarbamát zinečnatý, ethylenbisdithiokarmabát zinečnatý, ethylenbisdithiokarbamát manganatý, ethylendiamin-bis-dithiokarbamát manganatý a zinečnatý, tetramethylthiuramdisulfidy, amoniový komplex (Ν,Ν-ethylen-bis-dithiokarbamátu) zinečnatého, (N,N'-propylen-bis-dithiokarba25 mát) zinečnatý, N,N'-polypropylenbis(thiokarbamoyl)disulfíd, nitroderiváty, jako je dinitro-(l-methylheptyl)fenylkrotonát, 2-sek.butyl-4,6-dinitrofenyl-3,3dimethylakrylát, 2-sek.butyl-4,6-dinitrofenylizopropylkarbonát, diizopropyl-5-nitroizoftalát, heterocyklické látky, jako je 2-heptadecyl-2-imidazolinacetát, 2,4-dichlor-6-(o-chloranilino)s-triazin, Ο,Ο-diethylftalimidofosfonothioát, 5-amino-l -[bis(dimethylamino)fosfinyl]-3-fenyl-
1.2.4- triazol, 2,3-dikyan-l,4-dithioanhrachinon, 2-thio-l,3-dithiolo[4,5-b]chinoxalin, methyll-(butyl-karbamoyl)-2-benzimidazolkarbamát, 2-methoxykarbonylaminobenzimidazol, 2(furyl-(2))benzimidazol, 2-(thiazolyl-(4))benz-imidazol, N-( 1,1,2,2-tetrachlorethylthio)tetra- hydroftalimid, N-trichlormethylthiotetrahydroftalimid, N-trichlormethylthioftalimid, diamid N-dichlorfluormethylthio-N',N'-dimethyl-N-fenyl-sírové kyseliny, 5-ethoxy-3-trichlormethyl-1,2,3-thiadiazol, 2-thiokyanatomethylthiobenzthiazol, 1,4-dichlor-2,5-dimethoxybenzen, 4-(2-chlorfenylhydrazono)-3-methyl-5-izoxazolon, pyridin-2-thio-l-oxid, 40 8-hydroxychinolin a jeho soli smědí, 2,3-dihydro-5-karboxanilido-6-methyl-l,4-oxathiin,
2,3-dihydro-5-karboxanilido-6-methyI-l,4-oxathiin-4,4-dioxid, 2-methyl-5,6-dihydro-4Hpyran-3-karboxanilid, 2-methylfuran-3-karboxanilid, 2,5-dimethylfuran-3-karboxanilid,
2.4.5- trimethylfuran-3-karboxanilid, cyklohexyl-2,5-dimethyl-furan-3-karboxamid, N-cyklohexyl-N-methoxy-2,5-dimethylfiiran-3-karboxamid, 2-methylbenzanilid, 2-jodbenzanilid,
N-formyl-N-morfolin-2,2,2-trichlorethylacetal, piperazin-1,4-diylbis-(l-(2,2,2-trichlorethyl)formamid, l-(3,4-dichloranilino)-l-formylamino-2,2,2-trichlorethan, 2,6-dimethyl-N-tridecylmorfolin nebo jeho soli, N-[3-(p-terc-butylfenyl)-2-methylpropyl]-cis-2,6-dimethylmorfolin, N-[3-(p-terc.butylfenyl)-2-methylpropyl]-cis-2,6-dimethylmorfolin, N-[3-(pterc.butylfenyl)-2-methylpropyl]piperidin, l-[2-(2,4-dichlorfenyl)-4-ethyl-l,3-dichlorfenyl)50 4-n-propyl-l ,3-dioxolan-2-yl-ethyl]-l H-l ,2,4-triazol, N-(n-propyl)-N-(2,4,6-trichlorfenoxyethyl)-N'-imidazolylmočovina, l-(4-chlorfenoxy)-3,3-dimethyl-l-(l H-l ,2,4-triazoll-yl)-2-butanon, (2-chlorfenyl)-(4-chlorfenyl)-5-pyrimidinmethanol, 5-butyl-2-dimethylamino-4-hydroxy-6-methylpyrimidin, bis(p-chlorfenyl)-3-pyridinmethanol, 1,2-bis—(3ethoxykarbonyl)-2-thioureido)benzen, l,2-bis(3-methoxykarbonyl-2-thioureido)-benzen,
-4CZ 292552 B6 [2-(4-chlorfenyl)ethyl]-(l,l-dimethylethyl)-lH-l,2,4-triazol-l-ethanol, l-[3-(2-chlorfenyl)l-(4-fluorfenyl)oxiran-2-ylmethyl]-l H-1,2,4-triazol, a různé fungicidy, jako dodecylguanidinacetát, 3-[3-(3,5-dimethyl-2-oxycyklohexyl)-25 hydroxyethyljglutaramid, hexachlorbenzen, methyl-N-(2,6-dimethylfenyl)-N-(2-fuoryl)-DLalaninát, methylester DL-N-(2,6-dimethylfenyl)-N-(2'-methoxyacetyl)alaninu, N-(2,6-dimethylfenyl)-N-chloracetyl-DL-2-aminobutyrolakton, methylester DL-N-{2,6-dimethylfenyl)-N-(fenylacetyl)alaninu, 5-methyl-5-vinyl-3-(3,5-dichlorfenyl)-2,4-dioxo-l,3-oxazolidin-2,4-dion, 3-(3,5-dichlorfenyl)-l-izopropylkarbamoylhydantoin, N-(3,5-dichlorfenyl)10 1,2-dimethylcyklopropan-l ,2-dikarboximid, 2-kyan-[N-(ethylaminokarbonyl)-2methoximinojacetamid, l-[2-(2,4-dichlorfenyl)pentyl]-lH-l,2,4-triazol, 2,4-difluor-a-(lH-
1.2.4- triazolyl-l-methyl)-benzhydrylalkohol,N-(3-chlor-2,6-dinitro-4-trifluormethyl-fenyl)5-trifluormethyl-3-chlor-2-aminopyridin, l-((bis-(4-fluorfenyl)methylsilyl)methyl)-lH-
1.2.4- triazol.
Strobiluriny, jako je methyl-E-methoximino-[-(o-tolyloxy)-o-tolyl]acetát, methyl-E-{2-[6- I (2-kyanfenoxy)pyrimidin-4-yloxy]fenyl}-3-methoxyakrylát, methyl-E-methoximino-[a-(2fenoxyfenyl)]acetamid, methyl-E-methoximino-[a-(2,5-dimethylfenoxy)-o-tolyl]acetamid.
Anilinopyrimidiny, jako je N-(4,6-dimethylpyrimidin-2-yl)anilin, N-[4-methyl-6-(lpropinyl)pyrimidin-2-yl]anilin, N-(4-methyl-6-cyklopropylpyrimidin-2-yl)anilin.
Fenylpyrroly, jako je 4-(2,2-difluor-l ,3-benzodioxol-4-yl)pyrrol-3-karbonitril.
Amidy kyseliny skořicové, jako je 3-(4-chlorfenyl)-3-(3,4-dimethlxyfenyl)akryloylmorfolid.
(2RS, 3SR)-l-[3-(2-chlorfenyl)-2-[4-fluorfenyl]oxiran-2-ylmethyl]-lH-l,2,4-triazol.
Insekticidy:
abamectin, acephat, acrinathrin, alanycarb, aldicarb, alphamethrin, amitraz, avermectin, azadirachtin, azinphos A, azinphos M, azocyclotin, bacillus thuringiensis, bendiocarb, benfuracarb, bensultap, beta-cyluthrin, bifenthrin, BPMC, brofenprox, bromophos A, butencarb, buprofezin, butocarboxin, butylpyriadaben, cadusafor, carbaryl, carbofuran, carbophenothion, 35 carbosulfan, cartap, chloethocarb, chlorethoxyfos, chlorfenvinphos, chlorfluazuron, chlormephos, chlorpyrifos, chlorpyrifos M, cis-resmethrin, clocythrin, chlofentezin, cyanophos, cycloprothrin, cyfluthrin, cyhalothrin, cyhexatin, cypermethrin, cypromazin, deltamethrin, demeton M, demeton S, demeton-S-methyl, diafenthiuron, diazinon, dichlorfenthion, dichlorvos, dicliphos, dicrotophos, diethion, diflubenzuron, dimethoat, dimethylvinphos, dioxathion, disulfoton, 40 edifenphos, emamectin, esfenvalerat, ethiofencarb, ethion, ethofenprox, ethoprophos, etrimphos, fenamiphos, fenazaquin, fenbutatin oxide, fenitrothion, fenobucarb, fenothiocarb, fenoxycarb, fenpropathrin, fenpyrad, fenpyroximat, fenthion, fenvalerat, fipronil, fluazinam, flucycloxuron, fucythrinat, flufenoxuron, flufenprox, fluvalinat, fonophos, formohiton, fosthiazat, fubfenprox, furathiocarb, HCH, heptenophos, hexaflumuron, hexythiazox, imidacloprid, iprobenfos, isazofos, 45 izofenphos, izoprocarb, izoxathion, ivemectin lamda-cyhalothrin, lufenuron, malathion, mecarbam, mervinphos, mesulfenphos, metaldehyd, methacrifos, methamidophos, methidathion, methiocarb, methomyl, metolcarb, milbemectin, monocrotophos, moxidectin, naled, nitenpyram, omethoat, oxamyl, oxydemethon M, oxydeprofos, parathion A, parathion M, permethrin, phenthoat, phorat, phosalon, phosmet, phospphamdon, phoxim, pirimicarb, pirimiphos M, 50 primiphos A, profenofos, promecarb, propaphos, propoxur, prothiofos, prothiophos, prothoat, pymetrozin, pyraclofos, pyradaphenthion, pyresmethrin, pyrethrum, pyridaben, pyrimidifen, pyriproxifen, quinalphos, salithion, sebufos, silafluofen, sulfotep, sulprofos, tebufenozide, bebufenpyrad, tebupirimfos, teflubenzuron, tefluthrin, temephos, terba, terbufos, tetrachlorvinphos, thiafenox, thiodicarb, thiofanox, thiomethon, triazophos, triazuron, trichlorfon, 55 triflumuron, trimethacarb, vamidothion, XMC, xylylcarb, zetamethrin.
-5CZ 292552 B6
Dalšími vhodnými složkami jsou algicidy, moluscicidy a sloučeniny účinné na mořské živočichy, které se usazují například na nátěrech na dnech lodí.
Příklady provedení vynálezu
Příklady těchto přípravků jsou:
Příklad 1
Příklady přípravků v disperzních nátěrových hmotách nebo v disperzích plastických hmot:
a) 1000 dílů hmotnostních polymemí disperze na bázi polyakrylátu se nejprve zavede a smísí za míchání s 0,25 díly hmotnostními 20% hmotnostní suspenze koncentrátu 3-methyl-4-thiokyanato-5-aminoizothiazolu v propylenkarbonátu.
b) K hotové disperzi lze přidat práškovitou účinnou sloučeninu.
c) K zabudování do vodné a rozpouštědlo obsahující disperze plastické hmoty je vhodné přidat roztok 3 % hmotnostních 3-methyl^4-thiokyanato-5-aminoizothiazolu v propylenglykolu, dipropylengylkolu, fenoxyethanolu, fenoxypropanolu nebo polyethylenglykolu.
d) Pastu na bázi vody nebo glykolu obsahující 20 až 50 % hmotnostních 3-methyl-4—ghiokyanato-5-aminoizothiazlolu je vhodné zavést do vodné a rozpouštědlo obsahující disperze plastické hmoty.
e) Roztok 90 dílů hmotnostních 3-methyM-thiokyanato-5-aminoizothiazolu a 10 dílů hmot- nostních N-methylpyrrolidonu je vhodné zavést do vodné a rozpouštědlo obsahující disperze plastické hmoty.
f) Vodná disperze 20 dílů hmotnostních 3-methyl-4-thiokyanato-5-aminoizothiazolu, 25 dílů hmotnostních cyklohexanolu, 65 dílů hmotnostních frakce minerálního oleje vroucí při 210 až
2 80 °C a 10 dílů hmotnostních adičního produktu 40 mol ethylenoxidu na 1 mol ricinového oleje.
Směs této disperze s 100 000 díly hmotnostními vodné disperze nátěrové hmoty obsahuje 0,02 % účinné sloučeniny.
Příklad 2
Směs 14 dílů hmotnostních Cu(OH)2CuCC>3, 33 dílů hmotnostních monoethanolaminu, 22 dílů hmotnostncíh kyseliny benzoové, 11 dílů hmotnostních vody, 4 díly hmotnostní 3-methyl-4thiokyanato-5-aminoizothiazolu, 10 dílů hmotnostních ethoxylovaného nonylfenolu a 6 dílů hmotnostních propyleglykolu je zejména vhodná pro impregnaci dřeva.
Mikrobicidní prostředky nebo koncentráty používané k ochraně technických materiálů obsahující účinnou sloučeninu nebo kombinaci účinných sloučenin v koncentraci od 0,01 do 95, s výhodou 0,1 až 50 % hmotnostních.
Aplikované koncentrace účinných sloučenin, které se mají použít, závisí na druzích a výskytu mikroorganismů, které se mají kontrolovat, a na složení materiálu, který má být chráněn. Aplikované koncentrace jsou obvykle v rozmezí od 0,001 do 5 % hmotnostních, s výhodou od 0,05 do 1 % hmotnostního, vztaženo na materiál, který má být chráněn.
-6CZ 292552 B6
Biologické příklady
Příklad 1
Test na mikrotitrační desce - 1000, 500 a 250.10^* % hmotn. Účinná sloučenina vzorce Ic se rozpustí v acetonu. Do jamek mikrotitračních desek se umístí 100 μΐ kultivační půdy a ze zásobního roztoku se pipetují alikvotní podíly účinné sloučeniny, čímž se získají požadované koncentrace. Konečná koncentrace acetonu je 10 %. Testují se mikroorganismy, a to (bakterie) Citrobacter freundii, Escherichia coli, Próteus mirabilis, Pseudomonas aeruginosa a Staphylococcus aureus, (kvasinky) Candida albicans a Saccharomyces cerevisiae a (plísně) Altemaria altemata, Aspergillus niger a Penicillium funiculosum. Naočkované desky se inkubují při teplotě 23 °C (kvasinky a plísně) nebo 30 °C (bakterie). Růst mikroorganismů se vyhodnocuje po 2 (bakterie), 3 (kvasinky) nebo 5 dnech (plísně): ' testovaný organismus koncentrace účinné látky v .10“* % hmotn. i
000 500* 250
| Citrobacter freundii | 0 | 0 | 5 |
| Escherichia coli | 0 | 0 | H |
| Próteus mirabilis | 0 | 0 | 0 |
| Pseudomonas aeruginosa | 0 | 0 | 0 |
| Staphylococcus aureus | H | H | H |
| Candida albicans | 0 | 0 | H |
| Saccharomyces cerevisiae | 0 | 0 | H |
| Altemaria altemate | 0 | 0 | 0 |
| Aspergillus niger | 0 | 0 | 0 |
| Penicillium funiculosum | 0 | 0 | 0 |
| kontrola | 5 | 5 | 5 |
= žádný růst,
H = inhibice růstu = žádné působení, růst jako kontrola
Příklad 2
Konzervační zátěžový test v disperzi polymeru na bázi polyakrylátu
Hloubkové testy se provádí s disperzí polymeru na bázi polyakrylátu. Účinná sloučenina vzorce Ic se rozpustí v acetonu a přimíchá se k disperzi v koncentracích 500, 250 a 100.10-4 % hmotn. účinné látky. Disperze se potom naočkují („zatíží“) směsí mikroorganismů. Směs obsahuje mikroorganismy uvedené v biologickém příkladu 1. Pokusy se inkubují při teplotě 23 °C a očkují se znova každých 7 dnů. Po 6 cyklech se stanoví obsah mikroorganismu v disperzi.
Bylo zjištěno, že disperzi polymeru lze udržet prostou mikroorganismů za použití aplikované koncentrace 250.10-4 % hmotn. účinné látky.
Claims (8)
- PATENTOVÉ NÁROKY1. Použití aminoizothiazolů obecného vzorce IR X (I), kde10 R je atom vodíku nebo alkylová skupina s 1 až 4 atomy uhlíku aX je atom halogenu, NO2, CN nebo SCN, a jejich komplexů s kovy a jejich solí s kyselinami jako mikrobicidů pro ochranu technických 15 materiálů před napadením a zničením mikroorganismy.
- 2. Použití podle nároku 1, kde R je alkylová skupina s 1 až 4 atomy uhlíku a X je CN a SCN.
- 3. Použití podle nároku 1, kde R je methylová skupina.
- 4. Použití podle nároku 1, kde X v obecném vzorce I je thiokyanatoskupina.
- 5. Použití podle nároku 1, kdy se použije 3-methyl-4-thiokyanato-5-aminoizothiazol vzorce Ic.(Ic)
- 6. Způsob ochrany technických materiálů před napadením a zničením mikroorganismy, vyznačující se tím, že se technické materiály ošetří mikrobicidně účinnými množstvími aminoizothiazolů obecného vzorce I, jak jsou uvedeny v nároku 1.30
- 7. Způsob podle nároku 6, vyznačující se tím, že použitým mikrobicidem je3-methyl-4-thiokyanato-5-aminoizothiazol vzorce Ic, jak je uveden v nároku 3, v mikrobicidně účinných množstvích.
- 8. Způsob přípravy mikrobicidních prostředků, vyznačující se tím, že se smísí35 aminoizothiazol obecného vzorce I s inertním nosičovým materiálem a popřípadě s povrchově účinnými sloučeninami.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19654147A DE19654147A1 (de) | 1996-12-23 | 1996-12-23 | Verwendung von Aminoisothiazolen als Mikrobizide |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CZ226399A3 CZ226399A3 (cs) | 1999-10-13 |
| CZ292552B6 true CZ292552B6 (cs) | 2003-10-15 |
Family
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| Application Number | Title | Priority Date | Filing Date |
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| CZ19992263A CZ292552B6 (cs) | 1996-12-23 | 1997-12-09 | Použití aminoizothiazolů jako mikrobicidů |
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| Country | Link |
|---|---|
| US (1) | US6069161A (cs) |
| EP (1) | EP0946098B1 (cs) |
| JP (1) | JP2001508051A (cs) |
| KR (1) | KR20000062287A (cs) |
| CN (1) | CN1121140C (cs) |
| AT (1) | ATE204129T1 (cs) |
| AU (1) | AU742233B2 (cs) |
| BG (1) | BG63655B1 (cs) |
| BR (1) | BR9713614A (cs) |
| CA (1) | CA2275470A1 (cs) |
| CZ (1) | CZ292552B6 (cs) |
| DE (2) | DE19654147A1 (cs) |
| EA (1) | EA001604B1 (cs) |
| ES (1) | ES2163208T3 (cs) |
| HU (1) | HUP0000483A3 (cs) |
| IL (1) | IL130360A0 (cs) |
| NO (1) | NO313854B1 (cs) |
| NZ (1) | NZ336289A (cs) |
| PL (1) | PL334381A1 (cs) |
| TR (1) | TR199901454T2 (cs) |
| WO (1) | WO1998027816A1 (cs) |
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| BR9812042A (pt) * | 1997-09-08 | 2000-09-26 | Basf Ag | Uso de misturas |
| KR20010062209A (ko) * | 1999-12-10 | 2001-07-07 | 히가시 데쓰로 | 고내식성 막이 내부에 형성된 챔버를 구비하는 처리 장치 |
| US7048788B2 (en) * | 2003-08-05 | 2006-05-23 | Shunichi Yamazaki | Ship bottom paint using coal ash and diatomaceous earth |
| MX2007000095A (es) * | 2004-06-24 | 2007-03-21 | Vertex Pharma | Moduladores de transportadores con casete de union con atp. |
| JP5575179B2 (ja) * | 2011-06-07 | 2014-08-20 | ローム アンド ハース カンパニー | 安定な殺生物剤組成物 |
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| US4396413A (en) * | 1971-05-12 | 1983-08-02 | Rohm And Haas Company | Metal salt complexes of 3-isothiazolones as effective biocidal agents |
| US4032322A (en) * | 1976-06-18 | 1977-06-28 | Loren Kenneth Gibbons | Isothiazolylformamidine derivatives as herbicides |
| DE4328425A1 (de) * | 1993-08-24 | 1995-03-02 | Basf Ag | Acylamino-substituierte Isoxazol- bzw. Isothiazolderivate, Verfahren zu deren Herstellung und ihre Verwendung |
-
1996
- 1996-12-23 DE DE19654147A patent/DE19654147A1/de not_active Withdrawn
-
1997
- 1997-12-09 ES ES97952901T patent/ES2163208T3/es not_active Expired - Lifetime
- 1997-12-09 PL PL97334381A patent/PL334381A1/xx unknown
- 1997-12-09 AT AT97952901T patent/ATE204129T1/de not_active IP Right Cessation
- 1997-12-09 KR KR1019997005684A patent/KR20000062287A/ko not_active Abandoned
- 1997-12-09 AU AU56605/98A patent/AU742233B2/en not_active Ceased
- 1997-12-09 DE DE59704331T patent/DE59704331D1/de not_active Expired - Fee Related
- 1997-12-09 CZ CZ19992263A patent/CZ292552B6/cs not_active IP Right Cessation
- 1997-12-09 NZ NZ336289A patent/NZ336289A/xx unknown
- 1997-12-09 HU HU0000483A patent/HUP0000483A3/hu unknown
- 1997-12-09 CN CN97180949A patent/CN1121140C/zh not_active Expired - Fee Related
- 1997-12-09 IL IL13036097A patent/IL130360A0/xx unknown
- 1997-12-09 US US09/331,067 patent/US6069161A/en not_active Expired - Fee Related
- 1997-12-09 JP JP52830198A patent/JP2001508051A/ja not_active Withdrawn
- 1997-12-09 CA CA002275470A patent/CA2275470A1/en not_active Abandoned
- 1997-12-09 BR BR9713614-0A patent/BR9713614A/pt not_active Application Discontinuation
- 1997-12-09 WO PCT/EP1997/006854 patent/WO1998027816A1/de not_active Ceased
- 1997-12-09 TR TR1999/01454T patent/TR199901454T2/xx unknown
- 1997-12-09 EP EP97952901A patent/EP0946098B1/de not_active Expired - Lifetime
- 1997-12-09 EA EA199900539A patent/EA001604B1/ru not_active IP Right Cessation
-
1999
- 1999-06-22 BG BG103520A patent/BG63655B1/bg unknown
- 1999-06-22 NO NO19993079A patent/NO313854B1/no not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| CN1121140C (zh) | 2003-09-17 |
| IL130360A0 (en) | 2000-06-01 |
| CN1241907A (zh) | 2000-01-19 |
| EP0946098A1 (de) | 1999-10-06 |
| ATE204129T1 (de) | 2001-09-15 |
| BG63655B1 (bg) | 2002-08-30 |
| AU742233B2 (en) | 2001-12-20 |
| JP2001508051A (ja) | 2001-06-19 |
| ES2163208T3 (es) | 2002-01-16 |
| US6069161A (en) | 2000-05-30 |
| DE19654147A1 (de) | 1998-06-25 |
| NO993079D0 (no) | 1999-06-22 |
| EA001604B1 (ru) | 2001-06-25 |
| KR20000062287A (ko) | 2000-10-25 |
| NZ336289A (en) | 2000-03-27 |
| HUP0000483A2 (hu) | 2000-06-28 |
| AU5660598A (en) | 1998-07-17 |
| CZ226399A3 (cs) | 1999-10-13 |
| EA199900539A1 (ru) | 2000-02-28 |
| WO1998027816A1 (de) | 1998-07-02 |
| NO313854B1 (no) | 2002-12-16 |
| CA2275470A1 (en) | 1998-07-02 |
| EP0946098B1 (de) | 2001-08-16 |
| NO993079L (no) | 1999-06-22 |
| HUP0000483A3 (en) | 2001-02-28 |
| TR199901454T2 (xx) | 1999-08-23 |
| BR9713614A (pt) | 2000-04-11 |
| DE59704331D1 (de) | 2001-09-20 |
| PL334381A1 (en) | 2000-02-28 |
| BG103520A (en) | 2000-06-30 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PD00 | Pending as of 2000-06-30 in czech republic | ||
| MM4A | Patent lapsed due to non-payment of fee |
Effective date: 20061209 |