Abstract: Provided are a polymerizable composition for a dental material that can yield cured molded bodies having superior mechanical strength, a molded body obtained by curing the composition, and a dental material including the molded body. A polymerizable composition for a dental material, the polymerizable composition containing: one selected from the group consisting of allyl compound (A) and an oligomer of allyl compound (A); and (meth)acrylate compound (B).

Abstract: A method of producing a monomer composition including a polymerizable group-containing phosphoric acid compound is provided. The method includes a step of allowing a polymerizable group-containing alcohol compound, which is a compound not containing a urethane bond, to react with phosphorus pentoxide in the presence of a urethane compound, thereby obtaining a monomer composition including a polymerizable group-containing phosphoric acid compound.

Abstract: A dental adhesive composition containing: a (meth)acrylate compound (1) having an acidic group; and at least one polymerizable compound (2) selected from the group consisting of a cyclopolymerizable compound (2a) and a polymerizable compound (2b) having a cyclic structure and one polymerizable group.

Abstract: A urethane allyl compound having a urethane bond and an allyloxy group.

Abstract: A method of manufacturing a monomer composition includes a step of mixing a zinc catalyst (A), an iso(thio)cyanate compound (B) having an iso(thio)cyanate group, and an alcohol compound (C) having a hydroxy group, and at least one of the iso(thio)cyanate compound (B) or the alcohol compound (C) has a (meth)acryloyl group.

Abstract: Provided are a monomer which can provide a cured product having both high toughness and rigidity, a monomer composition containing the monomer, the monomer composition used as a dental material monomer composition, a dental material composition containing the monomer composition or the dental material monomer composition, a cured product thereof having excellent mechanical properties, a dental material formed by curing the dental material composition, a method for producing the monomer composition, and a method for producing the dental material. A (meth)acrylate (D) is a reaction product of an amine compound (A) having two or more amino groups, an iso(thio)cyanate compound (B) having two or more iso(thio)cyanato groups, and a hydroxy (meth)acrylate compound (C) having one or more polymerizable groups.

Abstract: A monomer composition, including: an acidic phosphoric acid ester (A); an amine-based catalyst (B); and a (meth)acrylate (E) having at least one of a urethane bond or a —NHC(?S)O— bond.

Abstract: A (meth)acrylate includes a compound (X) having a structure formed by a reaction of an epoxy compound (A) containing an epoxy group and a tertiary carbon atom or a quaternary carbon atom, a (meth)acrylic acid (B), and an iso(thio)cyanate compound (C) having two or more iso(thio)cyanate groups.

Abstract: A (meth)acrylate includes a reaction product of a thiol compound containing two or more thiol groups, and a (meth)acrylate compound containing two or more (meth)acryloyloxy groups.

Abstract: It is an object of the present invention to provide a monomer which can provide a cured product having both high toughness and rigidity. The present invention is a (meth)acrylate (D) which is a reaction product of a thiol compound (A) having two or more mercapto groups; an iso(thio)cyanate compound (B) having two or more iso(thio)cyanato groups; and a hydroxy (meth)acrylate compound (C) having one or more polymerizable groups.

Abstract: A polymerizable composition for an optical material includes an episulfide compound (A); an organic coloring matter (B); an UV absorber (C); and a polymerization catalyst (D), wherein the organic coloring matter (B) has a main absorption peak (P) between 565 nm and 605 nm in a visible light absorption spectrum, an absorption coefficient (ml/g·cm) of a peak apex (Pmax) exhibiting a maximum absorption coefficient of (P) is equal to or greater than 0.5×105, a peak width in an absorbance of ¼ of an absorbance of (Pmax) of (P) is equal to or less than 50 nm, a peak width in an absorbance of ½ of the absorbance of (Pmax) of (P) is equal to or less than 30 nm, and a peak width in an absorbance of ? of the absorbance of (Pmax) of (P) is in a range of equal to or less than 20 nm.

Abstract: Provided are a polymerizable composition for a dental material that can yield cured molded bodies having superior mechanical strength, a molded body obtained by curing the composition, and a dental material including the molded body. A polymerizable composition for a dental material, the polymerizable composition containing: one selected from the group consisting of allyl compound (A) and an oligomer of allyl compound (A); and (meth)acrylate compound (B).

Abstract: Provided are a monomer which can provide a cured product having both high toughness and rigidity, a monomer composition containing the monomer, the monomer composition used as a dental material monomer composition, a dental material composition containing the monomer composition or the dental material monomer composition, a cured product thereof having excellent mechanical properties, a dental material formed by curing the dental material composition, a method for producing the monomer composition, and a method for producing the dental material. A (meth)acrylate (D) is a reaction product of an amine compound (A) having two or more amino groups, an iso(thio)cyanate compound (B) having two or more iso(thio)cyanato groups, and a hydroxy (meth)acrylate compound (C) having one or more polymerizable groups.

Abstract: An optical material of the present invention has a minimum transmittance value in a wavelength range of 445 nm to 470 nm of a transmittance curve measured at a thickness of 2 mm of the optical material.

Abstract: A manufacturing method of an amine compound including obtaining a reaction solution containing an aldehyde compound by reacting a compound represented by Formula (a1) or (a2) with hydrogen and carbon monoxide in the presence of a metal compound of groups 8 to 10 and a phosphorus compound, neutralizing the reaction, purifying an aldehyde compound by distilling the neutralized reaction solution, and reacting the aldehyde compound with ammonia and with hydrogen in the presence of a catalyst to obtain an amine compound, wherein the phosphorus compound is represented by the Formula (R1O)3P, and the base compound is at least one selected from carbonate and hydrogen carbonate of metals of group I and carbonate and hydrogen carbonate of metals of group II, and wherein the neutralizing the reaction solution is performed within a temperature range of 40° C. to 50° C.

Abstract: A manufacturing method of an isocyanate compound including obtaining a reaction solution containing an aldehyde compound by reacting a compound represented by Formula (a1) or (a2) with hydrogen and carbon monoxide in the presence of a metal compound of groups 8 to 10 and a phosphorus compound, neutralizing the reaction solution, purifying an aldehyde compound by distilling the neutralized reaction solution, reacting the aldehyde compound with ammonia and with hydrogen in the presence of a catalyst to obtain an amine compound; and reacting the amine compound with a carbonylating agent to obtain an isocyanate compound, wherein the phosphorus compound is represented by the Formula (R1O)3P, and the base compound is at least one selected from carbonate and hydrogen carbonate of metals of group I and carbonate and hydrogen carbonate of metals of group II, wherein the neutralizing the reaction solution is performed within a temperature range of 40° C. to 50° C.

Abstract: A method of manufacturing a polymerizable composition for an optical material according to the present invention includes a step of mixing an iso(thio)cyanate compound (A1) and an organic coloring matter (B), so as to obtain a mixed solution a, a step of mixing the mixed solution a, an ultraviolet absorbing agent (D), and an iso(thio)cyanate compound (A2) which is identical to or different from the iso(thio)cyanate compound (A1), so as to obtain a mixed solution b, and a step of mixing a mixed solution b and an active hydrogen compound (C).

Abstract: An internal release agent includes at least one phosphodiester represented by the following general formula (1). In the formula, R1 and R2 independently represent a hydrocarbon group having 1 to 30 carbon atoms, which is optionally substituted with at least one hydroxyl group, and R3 represents an alkylene group having 2 to 4 carbon atoms. A plurality of R3's may be the same as or different from each other. M represents a hydrogen atom, an ammonium ion, an alkali metal ion, or a monovalent/divalent alkali earth metal ion, and n is an integer of 1 to 60.

Abstract: A polymerizable composition for an optical material includes an episulfide compound (A); an organic coloring matter (B); an UV absorber (C); and a polymerization catalyst (D), wherein the organic coloring matter (B) has a main absorption peak (P) between 565 nm and 605 nm in a visible light absorption spectrum, an absorption coefficient (ml/g·cm) of a peak apex (Pmax) exhibiting a maximum absorption coefficient of (P) is equal to or greater than 0.5×105, a peak width in an absorbance of ¼ of an absorbance of (Pmax) of (P) is equal to or less than 50 nm, a peak width in an absorbance of ½ of the absorbance of (Pmax) of (P) is equal to or less than 30 nm, and a peak width in an absorbance of ? of the absorbance of (Pmax) of (P) is in a range of equal to or less than 20 nm.

Abstract: Disclosed is a polymerizable composition for an optical material containing polyisocyanate (a) including aliphatic polyisocyanate (a1) and a modified aliphatic polyisocyanate (a2); and polythiol (b) having a di- or higher functional thiol group, in which the modified aliphatic polyisocyanate (a2) is contained in the polyisocyanate (a) in the amount of less than or equal to 60 weight %.