Abstract: The invention relates to a method for largely eliminating chlorine compounds from organic isocyanates or isocyanate mixtures by contacting said isocyanates or isocyanate mixtures with a water-containing inert gas flow or an organic material having a cation-exchanging effect. The inventive method allows the isocyanates to be gently freed from chorine-containing compounds and is particularly suitable for temperature-sensitive isocyanates.

Abstract: The invention relates to pharmaceutical compositions for nasal application, comprising selected CGRP antagonists which are described in WO 98/11128, as well as a process for the preparation thereof.

Abstract: The present invention relates to polyurethane cast elastomers which are prepared from higher molecular weight polyhydroxy compounds, durene diisocyanate and low molecular weight chain-lengthening and/or crosslinking agents. These elastomers are particularly useful for the production of moldings exposed to high mechanical stresses.

Abstract: The invention relates to pharmaceutical compositions for nasal application, comprising selected CGRP antagonists which are described in WO 98/11128, as well as a process for the preparation thereof.

Abstract: The present invention relates to polyurethane cast elastomers which are prepared from higher molecular weight polyhydroxy compounds, durene diisocyanate and low molecular weight chain-lengthening and/or crosslinking agents. These elastomers are particularly useful for the production of moldings exposed to high mechanical stresses.

Abstract: Durene diisocyanate is prepared by reacting durene with nitric acid in sulfuric acid, catalytic hydrogenation of the dinitrodurene that is formed, and phosgenation of the resultant durene diamine in a conventional manner. The intermediate products dinitrodurene and durene diamine do not have to be worked up in a complicated manner as solid products, but can be worked up in dissolved form. The intermediate products dinitrodurene and durene diamine do not have to be isolated and purified in a complicated manner. but can be processed directly after preparation. Another advantage of this process is that only a single organic solvent need be used for the overall preparation process. Separation and re-use of spent acid in the conversion of durene with nitric acid also renders the process of the present invention significantly less environmentally harmful than the known processes of the prior art.

Abstract: Isocyanates are prepared by a continuous process by reacting appropriate primary amines with phosgene in the presence of an isocyanate as solvent, the primary amine optionally dissolved in an inert organic solvent being reacted with phosgene, which is dissolved in the isocyanate, at temperatures of 60 to 150.degree. C. and at pressures of 1 to 30 bar (10.sup.5 to 3.10.sup.6 Pa) to obtain the corresponding isocyanate, wherein the molar ratio of phosgene to amine used is 4:1 to 1:1, and the isocyanate used as solvent is solids-free and has a value for hydrolysable chlorine of less than 2%.

Abstract: The present invention relates to mixtures of cycloaliphatic diisocyanates corresponding to formula 1) ##STR1## wherein R represents a saturated, linear, aliphatic hydrocarbon residue having 8 to 15 carbon atoms.The present invention also relates to a process for the preparation of these diisocyanate mixtures and to their use for the production of polyisocyanate addition products.

Abstract: Diisocyanates containing carboxylic acid ester groups corresponding to the formula: ##STR1## in which R and R.sup.1 represent specified groups are produced by phosgenation of the corresponding diamines, optionally present in the form of an ammonium salt. These diisocyanates are useful as starting materials in the production of plastics containing urethane and/or urea groups and as starting materials for the production of intermediate products used for the production of such plastics.