An epoxy resin, which is obtained by reacting at least a compound having one or more epoxy groups and a compound having a functional group that reacts with the epoxy groups, satisfies conditions (I) and/or (II): (I) the compound having a functional group that reacts with the epoxy groups includes a trihydric or higher phenol compound and/or a compound including a trifunctional or higher polyisocyanate; (II) the epoxy resin has an average degree of polyfunctionalization (X1) per molecule, as expressed by Formula (1), of 0.30 or more:

Average degree of polyfunctionalization (X1)=number of ends per molecule of epoxy resin−2.  Formula (1):

A resin composition for the secondary coating of an optical fiber is a resin composition containing a non-reactive urethane compound having a number average molecular weight of 10000 or more and 50000 or less, a photopolymerizable compound, and a photopolymerization initiator, the content of the non-reactive urethane compound is 0.05 parts by mass or more and 5 parts by mass or less based on the total amount of the resin composition, and the non-reactive urethane compound is a reaction product of a polyol having a number average molecular weight of 8000 or more and 20000 or less, a diisocyanate, and a compound having active hydrogen.

A nonaqueous coating material composition and a coating produced from the coating material composition are provided. The coating material composition contains at least one polyhydroxyl group-containing component, at least one polyisocyanate group-containing component, at least one catalyst, and at least one urethane additive (PF) which has specific groups. The urethane additive (PF) is prepared by reacting 0.5 to 20 mol % of the isocyanate groups originally present in a polyisocyanate (PI) with a component (Ia) and 10 to 99.5 mol % of the isocyanate groups originally present in the polyisocyanate (PI) with a component (IIa). The component (Ia) contains at least one perfluoroalkyl group of a specific formula and one group reactive toward the isocyanate groups. The component (IIa) contains at least one silane group of a specific formula and one group reactive toward the isocyanate groups.

Provided is an adhesive which, in a metal foil-containing laminated composite film used in a high temperature sterilization treatment, is resistant to the effects of moisture in the air during curing, has good workability when used as a solvent-free adhesive, and exhibits excellent adhesive strength and acid resistance. Provided is a method for producing an adhesive composition, the method including: a step of obtaining an alcohol-added isocyanate (E) by reacting a trifunctional or higher isocyanate compound (C2) and a monofunctional alcohol (D) at an equivalence ratio of isocyanate groups in the trifunctional or higher isocyanate compound (C2):monofunctional alcohol (D)=100 mol %:25 to 65 mol %, and a step of mixing a polyisocyanate (A) containing a trifunctional or higher isocyanate compound (C1) and the alcohol-added isocyanate (E), and an alcohol (B) having an acid value of 0.5 to 30 mgKOH/g, so that the equivalence ratio between isocyanate groups in the polyisocyanate (A) and hydroxyl groups in the alcohol (B) (isocyanate groups/hydroxyl groups) is within a range from 0.7 to 2.5.

Provided is an adhesive which, in a metal foil-containing laminated composite film used in a high temperature sterilization treatment, is resistant to the effects of moisture in the air during curing, has good workability when used as a solvent-free adhesive, and exhibits excellent adhesive strength and acid resistance. Provided is a method for producing an adhesive composition, the method including: a step of obtaining an alcohol-added isocyanate (E) by reacting a trifunctional or higher isocyanate compound (C2) and a monofunctional alcohol (D) at an equivalence ratio of isocyanate groups in the trifunctional or higher isocyanate compound (C2):monofunctional alcohol (D)=100 mol %:25 to 65 mol %, and a step of mixing a polyisocyanate (A) containing a trifunctional or higher isocyanate compound (C1) and the alcohol-added isocyanate (E), and an alcohol (B) having an acid value of 0.5 to 30 mgKOH/g, so that the equivalence ratio between isocyanate groups in the polyisocyanate (A) and hydroxyl groups in the alcohol (B) (isocyanate groups/hydroxyl groups) is within a range from 0.7 to 2.5.

An electrocoat system for electrodeposition is described. The system includes an inorganic bismuth-containing compound or a mixture of inorganic and organic bismuth-containing compounds. The system demonstrates a high degree of crosslinking and produces a cured coating with optimal crosslinking and corrosion resistance.

The present invention provides a blocked isocyanate composition comprising a blocked isocyanate compound in which an isocyanate group of an isocyanate compound is blocked with a fluoroalcohol compound, and at least one amidate compound represented by the following Formula (2):

##STR00001##

wherein B, G, J, R.sup.7. and R.sup.8 are as defined in the specification.

A method for deblocking a blocked isocyanate is described herein. The method includes contacting a blocked isocyanate and a halide ion source under conditions effective to provide a deblocked isocyanate. A method of making a polyurethane is also disclosed. The method of making a polyurethane includes combining a blocked isocyanate, a polyol, and a halide ion source in the presence of solvent and under conditions effective to provide the polyurethane.

A polyester-carbamate polymer and coating compositions containing the polymer are provided. The polyester-carbamate polymer preferably includes a polyester-carbamate backbone and one or more blocked isocyanate groups. A coating composition is provided that preferably includes the polyester-carbamate polymer and a thermoplastic dispersion. In a preferred embodiment, the coating composition is an organosol.

A polymer and a pharmaceutical composition employing the same are disclosed. The polymer includes a first repeating unit, a second repeating unit, and a third repeating unit. In particular, the first repeating unit is ##STR00001##
the second repeating unit is ##STR00002##
wherein R.sup.1 is C.sub.1-6 alkyl group; and the third repeating unit is ##STR00003##
wherein X is ##STR00004##
and Y is a hydrophilic polymeric moiety.