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    • 6. 发明授权
    • Surface-active compositions comprising a mixture of diphenyl ether and o-phenyl pheno
    • 包含二苯基醚和邻苯基苯酚的混合物的表面活性组合物
    • US07041631B2
    • 2006-05-09
    • US10901733
    • 2004-07-29
    • Dietmar OchsFrançois BruggerMarcel Schnyder
    • Dietmar OchsFrançois BruggerMarcel Schnyder
    • C11D3/48
    • C11D3/48C11D3/2068
    • A surface-active composition is described which comprises (a) from 0.01 to 90% by weight of a mixture of a microbicidal active ingredient of (a1) a diphenyl ether compound and (a2) a phenol derivative, (b) from 0 to 50% by weight of one or more hydrotropic agents, (c) from 0 to 80% by weight of one or more synthetic detergents or of a soap or of combinations of the mentioned substances and/or of a salt of a saturated and/or unsaturated C8–C22 fatty acid, (d) from 0 to 50% by weight of an alcohol, (e) from 0 to 50% by weight of typical ingredients for cleaning and disinfectant compositions and optionally (f) tap water or deionised water ad 100%. The compositions are used for the antimicrobial treatment of human skin and hair, of hard surfaces and of textile fibre materials.
    • 描述了一种表面活性组合物,其包含(a)0.01至90重量%的(a 1 SUB)二苯基醚化合物的杀微生物活性成分和(a 2 S 2 苯酚衍生物,(b)0至50重量%的一种或多种水溶助长剂,(c)0至80重量%的一种或多种合成洗涤剂或皂或其组合 所述物质和/或饱和和/或不饱和的C 8 -C 22脂肪酸的盐,(d)0至50重量%的 醇,(e)0至50重量%的用于清洁和消毒组合物的典型成分,以及任选地(f)100%自来水或去离子水。 该组合物用于人类皮肤和毛发,硬表面和纺织纤维材料的抗微生物处理。
    • 7. 发明授权
    • Use of phenylethylamine derivatives for the antimicrobial treatment of surfaces
    • 苯乙胺衍生物用于表面抗微生物处理
    • US06846492B2
    • 2005-01-25
    • US10204520
    • 2001-02-13
    • Wolfgang HaapWerner HölzlDietmar OchsKarin PetzoldMarcel Schnyder
    • Wolfgang HaapWerner HölzlDietmar OchsKarin PetzoldMarcel Schnyder
    • A01N33/10A01N37/38A01N39/00A01N39/02A01N39/04C07C217/60C07C255/54A01N25/00A61K7/075A61K7/50C11D7/00D06L1/00
    • C07C255/54A01N33/10A01N37/38A01N39/00A01N39/02A01N39/04C07C217/60C07C2601/08
    • The use of compounds of formula (1) is described, in which compounds R1, R2 and R3 are each independently of the others hydrogen; C1-C20alkyl; C3-C7cycloalkyl; C2-C20alkenyl; C4-C7cycloalkenyl; C2-C20alkynyl, C4-C7cycloalkynyl; or unsubstituted or C1-C5alkyl-, C3-C7cylcoalkyl-, C1-C5alkoxyl-, C3-C7cycloakoxy-, halo-, oxo-, carboxy-, carboxy-C1-C7alkyl ester-, carboxy-C3-C7cylcloalkyl ester-, cyano-, trifluoromethyl-, pentafluoroethyl-, amino-, N,N-mono- or di-C1-C20alkylamino- or nitro-substituted phenyl-C1-C5alkyl, naphthyl-C1-C5alkyl, phenylcarbonyl-C1-C5alkyl, naphthylcarbonyl-C1-C5alkyl, pyrrolylalkyl, furanylalkyl, thiophenylalkyl, pyrazolylalkyl, imidazolylalkyl, oxazolylalkyl, thiazolylalkyl, isoxazolylalkyl, isothiazolylalkyl, 1,2,3-triazolylalkyl, 1,2,4-triazolylalkyl, 1,2,3-oxadiazolylalkyl, 1,3,4-oxadiazolylalkyl, 1,2,3-thiadiazolylalkyl, 1,3,4-thiadiazolylalkyl, indolylalkyl, pyridylalkyl, pyridazinylalkyl, pyrimidinylalkyl, pyridazinylalkyl, quinolinylalkyl, isoquinolinylalkyl, pyrrolyl, furanyl, thiophenyl, pyrazolyl, imidazolyl, oxazolyl, thiazolyl, isoxazolyl, isothiazolyl, 1,2,3-triazolyl, 1,2,4-triazolyl, 1,2,3-oxadiazolyl, 1,3,4-oxadiazolyl, 1,2,3-thiadiazolyl, 1,3,4-thiadiazolyl, indolyl, pyridyl, pyridazinyl, pyrimidinyl, pyridazinyl, quinolinyl or isoquinolinyl; R4, R5, R6 and R7 are each independently of the others hydrogen; C1-C20alkyl; C3-C7 cycloalky; C2-C20alkenyl; C4-C7 cycloalkenyl; C2-C20alkynyl; or C4-C7 cycloalkynyl; and m and n are each independently of the other 0 or 1, for antimicrobial treatment of surfaces. The compounds exhibit a pronounced activity against pathogenic gram-positive and gram-negative bacteria, and also against yeasts and moulds. They are accordingly suitable for the antimicrobial treatment, especially preservation and disinfection, of surfaces.
    • 描述了式(1)化合物的用途,其中化合物R1,R2和R3各自独立地为氢; C1-C20烷基; C 3 -C 7环烷基; C2-C20烯基; C4-C7环烯基; C 2 -C 20炔基,C 4 -C 7环炔基; 或未取代的或C 1 -C 5烷基 - ,C 3 -C 7烷基烷基 - ,C 1 -C 5烷氧基 - ,C 3 -C 7环烷氧基 - ,卤代 - ,氧代 - ,羧基 - ,羧基-C 1 -C 7烷基酯 - ,羧基-C 3 -C 7环烷基酯 - 氰基 - 三氟甲基 - ,五氟乙基 - ,氨基 - ,N,N-单或二-C 1 -C 20烷基氨基或硝基取代的苯基-C 1 -C 5烷基,萘基-C 1 -C 5烷基,苯基羰基-C 1 -C 5烷基,萘基羰基-C 1 -C 5烷基 ,吡咯基烷基,呋喃基烷基,噻吩基烷基,吡唑基烷基,咪唑基烷基,恶唑基烷基,噻唑基烷基,异恶唑基烷基,异噻唑基烷基,1,2,3-三唑基烷基,1,2,4-三唑基烷基,1,2,3-恶二唑基烷基,1,3,4-恶二唑基烷基 1,2,3-噻二唑基烷基,1,3,4-噻二唑基烷基,吲哚基烷基,吡啶基烷基,哒嗪基烷基,嘧啶基烷基,哒嗪基烷基,喹啉基烷基,异喹啉基烷基,吡咯基,呋喃基,噻吩基,吡唑基,咪唑基,恶唑基,噻唑基,异恶唑基,异噻唑基, ,2,3-三唑基,1,2,4-三唑基,1,2,3-恶二唑基,1,3,4-恶二唑基,1,2,3-噻二唑基,1,3,4-噻二唑基,吲哚基, 吡啶基,哒嗪基,嘧啶基,哒嗪基,喹啉基或异喹啉基; R4,R5,R6和R7各自独立地为氢; C1-C20烷基; C3-C7环烷基; C2-C20烯基; C4-C7环烯基; C2-C20炔基; 或C 4 -C 7环炔基; m和n各自独立地为0或1,用于表面的抗微生物处理。 该化合物显示出对病原性革兰氏阳性的显着活性
    • 10. 发明授权
    • Hydroxyphenylvinylthiazoles
    • 羟基苯基乙烯基噻唑
    • US06624182B1
    • 2003-09-23
    • US09714716
    • 2000-11-16
    • Wolfgang HaapWerner HölzlDietmar OchsKarin PuchtlerMarcel Schnyder
    • Wolfgang HaapWerner HölzlDietmar OchsKarin PuchtlerMarcel Schnyder
    • A61K31425
    • C07D277/22A01N43/78C07D277/24
    • The use of hydroxyphenylvinylthiazoles of formula wherein R1, R2, R3 and R4 are each independently of the others hydrogen; halogen; hydroxy, C1-C16-alkyl, C1-C16alkoxy, phenyl; phenyl-C1-C3alkyl; C6-C10aryloxy, amino, mono-C1-C5alkyl-amino, di-C1-C5alkylamino or -NO2; wherein at least one of the radicals R1, R2, R3 and R4 is hydroxy; R5 is C1-C5alkyl; C1-C5alkoxy; or unsubstituted or halo-, C1-C5alkyl-, C1-C5alkoxy-, hydroxy- or pyrrolidinyl-substituted phenyl; as microbicidal active ingredients is described. The compounds exhibit a pronounced action against pathogenic gram-positive and gram-negative bacteria, and also against yeasts and moulds. Accordingly, they are suitable for the antimicrobial treatment, especially the preservation and disinfection, of surfaces.
    • 使用羟基苯基乙烯基噻唑的化合物R1,R2,R3和R4各自独立地为氢; 卤素; 羟基,C 1 -C 16 - 烷基,C 1 -C 16烷氧基,苯基; 苯基-C 1 -C 3烷基; C 1 -C 10芳氧基,氨基,单-C 1 -C 5烷基 - 氨基,二-C 1 -C 5烷基氨基或-NO 2; 其中基团R 1,R 2,R 3和R 4中的至少一个是羟基; R 5是C 1 -C 5烷基; C1-C5烷氧基; 或未取代或卤代 - ,C 1 -C 5烷基 - ,C 1 -C 5烷氧基 - ,羟基 - 或吡咯烷基 - 取代的苯基; 作为杀微生物活性成分被描述。 该化合物对病原性革兰氏阳性和革兰氏阴性细菌以及酵母和霉菌都表现出明显的作用。 因此,它们适用于抗菌处理,特别是表面的保存和消毒。