Abstract: The invention concerns macromonomers of a molecular weight of at least M≧500 g/mol containing siloxane groups. The macromonomers are usable as polymerizable monomers in a dental/medical composite comprising further at least a polymerizable monomer, an organic or inorganic acid or an acidic monomer, a stabilizer, an initiator, pigments and an organic or inorganic filler. The dental/medical composite is usable as a dental restorative material for filling and restoring teeth, making inlays and onlays, for artificial teeth, for sealing and surface modification materials, usable as temporary crown and bridge material. Furthermore, the macromonomers are usable for filler surface modification, as precursors for siloxane condensation products or as precursor for preparation of nanoparticles containing active polymerizable moieties.

Abstract: The invention concerns a dental composition comprising bisacrylamides that are polymerizable by free-radical polymerization and by Michael-addition polymerization with amines. The application of polymerization and addition polymerization with amines opens the possibility to completely reacted materials that have no oxygen inhibited layers. The claimed bisacrylamides have an improved hydrolytic stability.

Abstract: A process for the preparation of a polymerizable dental composition comprising the steps of

Abstract: Dental compositions comprising at least a polymerizable monomer and/or at least a polyaminoester that are prepared by reaction of bis- or polyacrylic esters and amines, pigments, organic and/or inorganic fillers, initiators and stabilizers.

Abstract: A composition from 0° C. to 40° C. and from 0 percent to 100 percent humidity, comprising from 0.2 to 5 percent by weight of at least a peroxide which decomposes by at most fifty percent by weight of the peroxide within 10 hours at a temperature of at least 75° C., from 0.2 to 3 percent by weight of a metal containing material, from 0.1 to 3 percent by weight of a protected reducing agent. The protected reducing agent is adapted to form an active reducing agent, from 0 to 1 percent by weight of an amine. The composition is formed from peroxide stored at from 0° C. to 40° C. and from 0 percent to 100 percent humidity for at least 24 hours.

Abstract: A low shrinking polymerizable dental material, includes a mixture of a polymerizable di- or poly(meth)acrylate, an alkoxylated bisphenol dimethacrylate, a polymerizable monomer, a polymerization initiator and/or sensitizer, a stabilizer and a filler in a content of 70 to 85 per cent. The volumetric shrinkage during polymerization is less than 2.0 Vol.-%.

Abstract: The synthesis of self-adhesive polymerizabe monomers and their application as a water containing and a water free self-adhesive dental/medical composite is described. The dental/medical composite comprises a self-adhesive polymerizabe monomer, a polymerizable monomer, an acid-reactive and/or reactive and/or non-reactive filler, a diluent, a polymerization initiator and a stabilizer. As polymerization initiators are used the commonly known thermal initiators, redox initiators and/or photo initiators. The new adhesive dental composite develops adhesion to dentine of about 4 MPa. Fillers of high X-ray absorbance provide radio-opacity values grater than that of the same thickness of aluminium.

Abstract: Dental composition having an improved light and thermal stability, including a mixture of at least a polymerizable resin, at least a polymerizable monomer, at least a polymerization initiator and/or a sensitizer and stabilizer, and at least an organic and/or inorganic filler and pigments in a content of 0 to 90 percent and at least one of the stable radicals.

Abstract: A composition including nanoparticles each having an acidic polymerizable siloxane moiety. For example, a hydrolysis stable, self-etching, self-priming dental adhesive composition including 90 to 10 percent by weight of an aqueous phase, and 10 to 90 percent by weight of acidic polymerizable nanoparticles. The acidic polymerizable nanoparticles are obtainable by hydrolysis of a mixture containing one or more hydrolyzable organosilicon compounds wherein (i) at least a portion of the hydrolyzable organosilicon compounds contains one or more polymerizable groups and (ii) at least a portion of the hydrolyzable organosilicon compounds contain one or more acidic moieties.

Abstract: The invention concerns a dental composition comprising bisacrylamides that are polymerizable by free-radical polymerization and by Michael-addition polymerization with amines. The application of polymerization and addition polymerization with amines opens the possibility to completely reacted materials that have no oxygen inhibited layers. The claimed bisacrylamides have an improved hydrolytic stability.

Abstract: The invention describes a low shrinking polymerizable dental material, comprising a mixture of a polymerizable resin, a polymerizable monomer, a polymerization initiator and/or sensibilizer and a filler in a content of about 20 to about 85 percent. The volumetric shrinkage during polymerization is less than about 1.5 Vol.-% due to its rheopex behavior.

Abstract: Dental compositions comprising at least a polymerizable monomer and/or at least a polyaminoester that are prepared by reaction of bis- or polyacrylic esters and amines, pigments, organic and/or inorganic fillers, initiators and stabilizers.

Abstract: The invention concerns a dental composition comprising bisacrylamides that are polymerizable by free-radical polymerization and by Michael-addition polymerization with amines. The application of polymerization and addition polymerization with amines opens the possibility to completely reacted materials that have no oxygen inhibited layers. The claimed bisacrylamides have an improved hydrolytic stability.

Abstract: A dental adhesive composition for bonding dental restoratives to dentin and enamel provides a one-part self-etching, self-priming dental adhesive composition having hydrolysis stable polymerizable acidic adhesive monomers.

Abstract: The invention concerns macromonomers of a molecular weight of at least M≧500 g/mol containing siloxane groups. The macromonomers are usable as polymerizable monomers in a dental/medical composite comprising further at least a polymerizable monomer, an organic or inorganic acid or an acidic monomer, a stabilizer, an initiator, pigments and an organic or inorganic filler. The dental/medical composite is usable as a dental restorative material for filling and restoring teeth, making inlays and onlays, for artificial teeth, for sealing and surface modification materials, usable as temporary crown and bridge material. Furthermore, the macromonomers are usable for filler surface modification, as precursors for siloxane condensation products or as precursor for preparation of nanoparticles containing active polymerizable moieties.

Abstract: A method of venting during sealing the cartridge. The cartridge body has an external wall, a generally cylindrical internal chamber wall having an internal chamber wall diameter and enclosing a cartridge chamber, and at least one channel wall forming a channel (or groove) in the chamber wall. The piston has a generally cylindrical plug wall positioned adjacent to the generally cylindrical internal chamber wall. The cylindrical plug wall has a diameter substantially equal to the diameter of the cylindrical internal chamber wall. Dental material is conveyed into the cartridge chamber. The piston is pressed into the cartridge chamber while venting gas from the cartridge chamber through the channel prior to forming a hermetic seal around the dental material in the cartridge chamber.

Abstract: A composition from 0° C. to 40° C. and from 0 percent to 100 percent humidity, comprising from 0.2 to 5 percent by weight of at least a peroxide which decomposes by at most fifty percent by weight of the peroxide within 10 hours at a temperature of at least 75° C., from 0.2 to 3 percent by weight of a metal containing material, from 0.1 to 3 percent by weight of a protected reducing agent. The protected reducing agent is adapted to form an active reducing agent, from 0 to 1 percent by weight of an amine. The composition is formed from peroxide stored at from 0° C. to 40° C. and from 0 percent to 100 percent humidity for at least 24 hours.

Abstract: A dental composition including a mono- and/or a poly-cyanoacrylate, a polymerizable monomer, a stabilizer, an initiator, and optionally, pigments and a filling material.

Abstract: An esterified macromonomer within the scope of the general formula: 1

Abstract: A self-curing dental adhesive has at least one polymerizable resin; at least one polymerizable monomer; at least one polymerizable monomer with an acidic moiety selected from the group 1