Are acids considered to be protophobic
Translation of "N-methylpyrrolidone" in German
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The concentrate of claim 5 wherein the first component is N-methylpyrrolidone.
A dye solution according to claim 1, which comprises caprolactam or N-methylpyrrolidone.
Dye solutions according to claim 1, characterized in that they are caprolactam or N-methylpyrrolidone contain.
The process of one or more of claims 1 to 4, wherein the amide is a cyclic carboxamide or sulfonamide, preferably N-methylpyrrolidone.
Method according to one or more of claims 1 to 4, characterized in that the acid amide is a cyclic carboxylic or sulfonic acid amide, preferably N-methyl-pyrrolidone, is.
Conventional liquid activator systems for casting polyamides by anionic polymerization (AP) of caprolactam contain isocyanates mixed with pyrrolidones such as N-methylpyrrolidone (NMP) or N-ethylpyrrolidone (NEP).
Conventional liquid activator systems for the production of cast polyamide by anionic polymerization of caprolactam contain isocyanates, which like pyrrolidones N-methyl pyrrolidone (NMP) or N-ethyl-pyrrolidone (NEP) are mixed.
A microemulsion cleaning composition according to claim 4, wherein the pyrrolidone compound is N-methylpyrrolidone.
A microemulsion detergent according to claim 4, wherein the pyrrolidone compound N-methylpyrrolidone is.
A process according to claim 6 wherein the N-alkyl cyclic amide is N-methylpyrrolidone or N-methylpiperidone.
The method of claim 6 in which the N-alkyl cyclic amide N-methylpyrrolidone or is N-methylpiperidone.
An ink according to Claim 4 wherein the heterocyclic ketone is N-methylpyrrolidone.
The ink of claim 4, wherein the heterocyclic ketone is selected from N-methylpyrrolidone consists.
The pair of materials are NPM (N-methylpyrrolidone) as solvent and TFE (trifluoroethanol) as coolant.
A pair of substances containing NPM (N-methylpyrrolidone) as a solvent and also a refrigerant made of TFE (trifluoroethanol), is used for sorption heating or cooling processes.
A solution as claimed in claim 7, containing phenothiazine and N-methylpyrrolidone.
A method according to claim 1 or 2, wherein said aprotic protophobic polar solvents include acetonitrile, sulfolane, 3-sulfolane and N-methylpyrrolidone.
Process according to claim 1 or 2, wherein the aprotic, protophobic, polar solvents are acetonitrile, sulfolane, 3-sulfolane and N-methylpyrrolidone include.
The compositions according to claim 2, wherein the liquid carrier is selected from water, N-methylpyrrolidone, vegetable oils, glycols.
Compositions according to claim 2, wherein the liquid carrier is selected from water, N-methylpyrrolidone, Vegetable oils and glycols.
The process according to anyone of claims 18-20 wherein said aprotic solvent used in step (a) to dissolve the biocompatible polysaccharide polymer is selected from dimethylsulfoxide and N-methylpyrrolidone.
A method according to any one of claims 18 to 20, wherein said aprotic solvent used in step (a) to dissolve the biocompatible polysaccharide polymer is selected from dimethyl sulfoxide and N-methylpyrrolidone.
A composition as claimed in any preceding Claim, characterized in that the solvent is selected from lower alcohols, N-methylpyrrolidone and water.
A mixture as claimed in any preceding claim, characterized in that the solvent is composed of lower alcohols, N-methylpyrrolidone and water is selected.
The casting solution of claim 31 wherein the solvent is N-methylpyrrolidone, formamide, dimethylformamide, dimethylsulfoxide, dimethylacetylacetamide, or 4-butyrolactone.
The casting solution of claim 31, wherein the solvent N-methylpyrrolidone, Formamide, dimethylformamide, dimethyl sulfoxide, dimethylacetylacetamide or 4-butyrolactone.
The control solution of Claim 4 wherein the mediator is a ferricyanide and the solvent is ethylene glycol, N-methylpyrrolidone or n-propanol.
Comparison solution according to claim 4, wherein the mediator is a ferricyanide and the solvent is ethylene glycol, N-methylpyrrolidone or n-propanol.
Process according to Claim 5, characterized in that, in the separation of benzene, the selective solvent employed is N-methylpyrrolidone.
Process according to Claim 5, characterized in that, in the separation of benzene, with N-methylpyrrolidone is operated as a selective solvent.
The coating of claims 1 wherein the organic solvent is selected from dimethylformamide, N-methylpyrrolidone, ethyl acetate, xylene and mixtures thereof.
Coating according to claim 1, wherein the organic solvent is selected from dimethylformamide, N-methylpyrrolidone, Ethyl acetate, xylene, and mixtures thereof.
The process according to claim 4, characterized in that the above-mentioned neutralizing agent is selected from N-methylpyrrole, N-methylpyrrolidone, N-methylpyrrolidine, N-methylpiperidine, N-methylmorpholine and N-hydroxyethylmorpholine.
Process according to claim 4, characterized in that the aforementioned neutralizing agent consists of N-methylpyrrole, N-methylpyrrolidone, N-methylpyrrolidine, N-methylpiperidine, N-methylmorpholine and N-hydroxyethylmorpholine is selected.
A process for manufacturing a polysulfone membrane as defined in any one of Claims 7 to 11, wherein said common solvent is N-methylpyrrolidone.
A method for producing a polysulfone membrane according to any one of claims 7 to 11, wherein the common solvent N-methylpyrrolidone is.
Agents for the treatment of worm diseases, which contain praziquantel in concentrations of 0.1-20 per cent by weight as well as N-methylpyrrolidone.
Agent for the dermal treatment of worm diseases containing praziquantel in concentrations of 0.1-20 percent by weight N-methylpyrrolidone contain.
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