Abstract: The present disclosure relates to an anticoagulant-coated microporous hollow fiber membrane showing reduced thrombogenicity. The disclosure further relates to a method for producing the membrane and a filtration and/or diffusion device comprising the membrane.

Abstract: The invention relates to a method for producing 3,7-diaza-bicyclo[3.3.1]nonane metal complexes, wherein the ligand, a 3,7-diaza-bicyclo[3.3.1]nonane compound, is reacted with an aqueous metal(II)salt solution in one step. According to the invention, the reaction stage is carried out with water as solvent.

Abstract: The invention relates to a one-pot reaction for the production of 3,7-diaza-bicyclo[3.3.1]nonane compounds, wherein in a first step a dicarboxylic acid ester is reacted with a pyridine aldehyde and a primary amine. The piperidone created in this manner is reacted with formaldehyde and a further primary amine in a second step. It is essential to the invention that both reaction steps are carried out in a one-pot variation in a C1-C4 alcohol as the solvent, and that the reaction water created is removed by means of distillation.

Abstract: The present invention relates to a process for the preparation of 3,7-diazabicyclo[3.3.1]nonane compounds. According to the invention, in a first step, a dicarboxylic acid ester is reacted with a pyridine aldehyde and a primary amine. The piperidone which forms is reacted in a second stage with formaldehyde and a further primary amine. It is essential to the invention that, in the first reaction stage, a C2-C4-alcohol is used as solvent and, in the second reaction stage, a C3-C4-alcohol is used as solvent.

Abstract: The invention relates to a method for producing 3,7-diaza-bicyclo[3.3.1]nonane metal complexes, wherein the ligand, a 3,7-diaza-bicyclo[3.3.1] nonane compound, is reacted with an aqueous metal(II)salt solution in one step. According to the invention, the reaction stage is carried out with water as solvent.

Abstract: The invention relates to a method for producing the compositions cited in the title. According to this method: dipyridyl ketone is reacted with hydroxylamine; the oxime obtained thereby is reduced without intermediate isolation to form 1,1-di-(2-pyridyl)-methylamine, and; this amine is firstly reacted with 1 to 1.5 molar equivalent of picolyl chloride and then with another 1 to 1.5 molar equivalent of picolyl chloride to form the amine of formula (1). This amine is purified via the tetrafluoroborate salt and subsequently alkylated with an alkyl iodide. This method represents an improvement with regard to prior art methods for producing these compounds.

Abstract: The invention relates to a one-pot reaction for the production of 3,7-diaza-bicyclo[3.3.1]nonane compounds, wherein in a first step a dicarboxylic acid ester is reacted with a pyridine aldehyde and a primary amine. The piperidone created in this manner is reacted with formaldehyde and a further primary amine in a second step. It is essential to the invention that both reaction steps are carried out in a one-pot variation in a C1-C4 alcohol as the solvent, and that the reaction water created is removed by means of distillation.

Abstract: The invention relates to a method for the production of bleaching catalyst granules, containing a bleaching catalyst, an acidic polymer, a support material and optionally further adjuncts, characterized in that a fluid bed is formed from the support material in a fluidized bed apparatus, an aqueous solution or dispersion is added to the fluid bed, containing the bleaching catalyst, the acidic polymer, and optionally the further adjuncts which is then granulated and dried. The method is particularly suitable for bleaching catalysts of formula (1), where R, R1, R2, R3 and X have the meanings given in the description.

Abstract: The present invention relates to a process for the preparation of 3,7-diazabicyclo[3.3.1]nonane compounds. According to the invention, in a first step, a dicarboxylic acid ester is reacted with a pyridine aldehyde and a primary amine. The piperidone which forms is reacted in a second stage with formaldehyde and a further primary amine. It is essential to the invention that, in the first reaction stage, a C2-C4-alcohol is used as solvent and, in the second reaction stage, a C3-C4-alcohol is used as solvent.

Abstract: The invention relates to a method for producing the compositions cited in the title. According to this method: dipyridyl ketone is reacted with hydroxylamine; the oxime obtained thereby is reduced without intermediate isolation to form 1,1-di-(2-pyridyl)-methylamine, and; this amine is firstly reacted with 1 to 1.5 molar equivalent of picolyl chloride and then with another 1 to 1.5 molar equivalent of picolyl chloride to form the amine of formula (1). This amine is purified via the tetrafluoroborate salt and subsequently alkylated with an alkyl iodide. This method represents an improvement with regard to prior art methods for producing these compounds.

Abstract: The invention relates to construction materials, in particular concrete, which contain polyester fibers. The polyester fibers are treated with an oligoester to improve their incorporation into the construction materials.

Abstract: The invention relates to detergents and cleaning agents that contain both a dye fixative and a soil-release polymer. According to the invention, the dye fixatives used are (a) reaction products of polyamines and cyanamides and organic and/or inorganic acids, or cyanamides and aldehydes and ammonium salts, or cyanamides and aldehydes and amines, or amines and epichlorohydrin, (b) the group containing polyamines and polyamine derivatives, (c) the group containing polyimines and polyimine derivatives, (d) the group of cationic polyelectrolytes, (e) the group containing polymers that comprise imidazoline units or (f) the group containing bis(chloromethyl)biphenyl polyquat.

Abstract: The following dye-transfer-inhibiting dye fixatives are used in laundry detergents which comprise nonionic surfactants: Reaction products of a) amines with epichlorohydrin or b) cyanamide with amines and aldehydes.

Abstract: The following dye-transfer-inhibiting dye fixatives are used in laundry detergents: Reaction products of a) polyamines with cyanamides and amidosulfuric acid or b) cyanamides with aldehydes and ammonium salts or c) amines with epichlorohydrin.

Abstract: The following dye-transfer-inhibiting dye fixatives are used in laundry detergents:

Abstract: The following dye-transfer-inhibiting dye fixatives are used in laundry detergents which comprise nonionic surfactants:

Abstract: The invention relates to oligoesters obtained by polycondensation ofa) from 40 to 52 mol %, preferably from 45 to 50 mol %, of one or more dicarboxylic acids or esters thereof,b) from 10 to 40 mol %, preferably from 20 to 35 mol %, of ethylene glycol and/or propylene glycol,c) from 3 to 20 mol %, preferably from 10 to 15 mol %, of polyethylene glycol,d) from 0.5 to 10 mol %, preferably from 1 to 7.5 mol %, of a water-soluble addition product of from 5 to 80 mol of an alkylene oxide with 1 mol of C.sub.1 -C.sub.24 -alcohols, C.sub.6 -C.sub.18 -alkylphenols or C.sub.8 -C.sub.24 -alkylamines ande) from 0.4 to 10 mol %, preferably from 0.5 to 8 mol %, of one or more polyols having from 3 to 6 hydroxyl groups.These oligoesters are used as soil release polymers in detergents.

Abstract: The present Application relates to a process for the preparation of N-lauroyl-L-glutamic acid di-n-butylamide by reaction of N-lauroyl-L-glutamic acid dimethyl ester with n-butylamine in the presence of a hydrocarbon or hydrocarbon mixture as an auxiliary solvent.

Abstract: The present invention relates to a process for the preparation of dimethyl N-lauroyl-L-glutamate by reaction of N-lauroyl-L-glutamic acid with methanol in the presence of trimethyl orthoformate.

Abstract: Method for avoiding network defects due to unwanted secondary reactions during the polymerization in water-swellable hydrophilic polymers which contain polymers prepared by free radical (co)polymerization of one or more hydrophilic monomers of the formula I ##STR1## wherein R.sup.1 is hydrogen, methyl or ethyl,R.sup.2 is the group --COOR.sup.4, the sulphonyl group, the phosphonyl group, the phosphonyl group-esterified by (C.sub.1 -C.sub.4)-alkanol or a group of the formula ##STR2## R.sup.3 is hydrogen, methyl, ethyl or the carboxyl group, R.sup.4 is hydrogen, amino or hydroxy-(C.sub.1 -C.sub.4)-alkyl andR.sup.5 is the sulphonyl group, the phosphonyl group or the carboxyl group, or grafting (co)polymerization of one or more hydrophilic monomers of the formula I onto a grafting base, using a free radical initiator which forms three or more free radical sites per molecule.