Abstract: Substituted guanidine derivatives of the formula I ##STR1## are prepared by reacting calcium cyanamide with a primary or secondary amino carboxylic acid or a primary or secondary amino sulfonic acid or their derivatives of the formula II ##STR2## where the substituents R.sup.1 and R.sup.2 have the meanings explained in the description.

Abstract: A process for preparing guanidine derivatives, in particular creatine, is described and entails an O-alkylisourea salt and a primary or secondary amine being reacted in the presence of crystals of a guanidine derivative.

Abstract: Substituted guanidine derivatives of the formula I ##STR1## are prepared by a) converting urea into an alkylated isourea of the formula II ##STR2## and b) reacting the alkylated isourea with a primary or secondary amine of the formula III ##STR3## where the substituents R.sup.1, R.sup.2 and R.sup.10 have the meanings explained in the description.

Abstract: A process for the preparation of water-soluble, amino-containing condensates and adducts having a greater drainage and retention effect in papermaking, in which from 5 to 95% by weight of the condensates or adducts are separated off as permeate from solutions of water-soluble, amino-containing condensates or adducts by ultrafiltration through membranes and the amino-containing condensates or adducts having improved efficiency are, if required, isolated from the retentate, and the high molecular weight polymer fractions contained in the retentate are used as retention aids, drainage aids and fixing compositions in papermaking, as promoters in the sizing of paper with alkyldiketenes, as flocculants for sewage sludges, as adhesion promoters in the production of laminated films, as additives for hair and skincare compositions and as compositions for immobilizing anionic active ingredients.

Abstract: Substituted guanidine derivatives of the formula I, ##STR1## are prepared by reacting haloformamidinium salts of the formula II, ##STR2## where Hal can be Cl, F, Br and I, with primary or secondary amines of the formula III ##STR3## where the substituents R.sup.1 and R.sup.2 have the meanings explained in the description.

Abstract: Substituted guanidine derivatives of the formula I, ##STR1## are prepared by a) reacting calcium cyanamide with an alcohol of the formula R.sup.10 --OH to give an isourea derivative of the formula II, ##STR2## and b) reacting the substituted isourea with a primary or secondary amine of the formula III, ##STR3## where the substituents R.sup.1 and R.sup.2 and R.sup.10 have the meanings explained in the description.

Abstract: Aqueous alkyldiketene dispersions which contain a C.sub.14 -C.sub.22 -alkyldiketene and from 1 to 10% by weight of a polymeric protective colloid contain, as the protective colloid(a) copolymers of(1) N-vinylpyrrolidone and(2) at least one quaternized N-vinylimidazole or a substituted quaternized N-vinylimidazoleas polymerized units in a molar ratio of from 80:20 to 5:95 and have a K value of at least 20 (according to H. Fikentscher in 0.5 M aqueous sodium chloride solution at a polymer concentration of 0.1% by weight and at 25.degree. C.) or(b) condensates which are obtainable by(1) partial amidation of polyethyleneimines with monocarboxylic acids and, if required(2) condensation of the partially amidated polyethyleneimines with at least bifunctional crosslinking agents which have a halohydrin, glycidyl, aziridine or isocyanate unit or a halogen atom as a functional groupto give crosslinked, amidated polyethyleneimines which have a viscosity of at least 100 mPa.

Abstract: Aqueous latent-crosslinking polyurethane dispersions, comprisingI) a disperse phase (P.I) includingIa) polyurethanes (PUR.Ia) carrying not only groups which render the polyurethane dispersible in water but also groups with a C--C double bond which is activated by a carbonyl attached directly to it, orIb) a mixture ofa polyurethane (PUR.Ib) carrying groups which render the polyurethane dispersible in water but no groups with a C--C double bond which is activated by carbonyl attached directly to it, anda compound (V.I) different from the polyurethanes PUR.Ia and PUR.Ib, which carries groups with a C--C double bond which is activated by a carbonyl attached directly to it, andII) a compound havingon average at least 2 hydrogens present as amino function,a solubility in water of more than 1 g/l (25.degree. C.) anda number-average molecular weight (M.sub.n) of from 200 to 1,000,000 (compound II).

Abstract: A process for the preparation hydroxyoxaalkylmelamines of the general formula I ##STR1## in which R.sup.1 denotes a residue of the general formula II ##STR2## in which the radicals R' can be the same or different and stand for hydrogen or C.sub.1 -C.sub.4 alkyl and n denotes 2 or 3 and the radicals R.sup.2 and R.sup.3 stand for one of the radicals R.sup.1 or hydrogen, by the reaction of melamine with a compound of the general formula III ##STR3## in which R' and n have the meanings stated above, at a temperature of from 120.degree. to 250.degree. C. and in the presence of an acid catalyst, in which the acid catalyst is used in a concentration of from 0.01 to 0.15 mol and preferably from 0.02 to 0.12 mol and more preferably from 0.03 to 0.1 mol, based on 1 mol of melamine.