The patent badge is an abbreviated version of the USPTO patent document. The patent badge does contain a link to the full patent document.
The patent badge is an abbreviated version of the USPTO patent document. The patent badge covers the following: Patent number, Date patent was issued, Date patent was filed, Title of the patent, Applicant, Inventor, Assignee, Attorney firm, Primary examiner, Assistant examiner, CPCs, and Abstract. The patent badge does contain a link to the full patent document (in Adobe Acrobat format, aka pdf). To download or print any patent click here.
Patent No.:
Date of Patent:
Jan. 25, 2005
Filed:
Feb. 13, 2001
Wolfgang Haap, Grenzach-Wyhlen, DE;
Werner Hölzl, Eschentzwiller, FR;
Dietmar Ochs, Schopfheim, DE;
Karin Petzold, Fischingen, DE;
Marcel Schnyder, Birsfelden, CH;
Wolfgang Haap, Grenzach-Wyhlen, DE;
Werner Hölzl, Eschentzwiller, FR;
Dietmar Ochs, Schopfheim, DE;
Karin Petzold, Fischingen, DE;
Marcel Schnyder, Birsfelden, CH;
Ciba Specialty Chemicals Corporation, Tarrytown, NY (US);
Abstract
The use of compounds of formula (1) is described, in which compounds R, Rand Rare each independently of the others hydrogen; C-Calkyl; C-Ccycloalkyl; C-Calkenyl; C-Ccycloalkenyl; C-Calkynyl, C-Ccycloalkynyl; or unsubstituted or C-Calkyl-, C-Ccylcoalkyl-, C-Calkoxyl-, C-Ccycloakoxy-, halo-, oxo-, carboxy-, carboxy-C-Calkyl ester-, carboxy-C-Ccylcloalkyl ester-, cyano-, trifluoromethyl-, pentafluoroethyl-, amino-, N,N-mono- or di-C-Calkylamino- or nitro-substituted phenyl-C-Calkyl, naphthyl-C-Calkyl, phenylcarbonyl-C-Calkyl, naphthylcarbonyl-C-Calkyl, 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; R, R, Rand Rare each independently of the others hydrogen; C-Calkyl; C-Ccycloalky; C-Calkenyl; C-Ccycloalkenyl; C-Calkynyl; or C-Ccycloalkynyl; 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.