Abstract: The thiol-containing composition for an optical material of the present invention includes a compound (A) represented by General Formula (a), and a compound (B) composed of at least one selected from a compound (b2-1) represented by General Formula (b2-1), a compound (b3-1) represented by General Formula (b3-1), a compound (b3-2) represented by General Formula (b3-2), and a compound (b4-2) represented by General Formula (b4-2), in which, in high-performance liquid chromatography measurement, the total peak area ratio of the compound included in the compound (B) is 0.1% to 60.0% with respect to the peak area 100 of the compound (A).

Abstract: The thiol-containing composition for an optical material of the present invention includes a compound (A) represented by General Formula (a), and a compound (B) composed of at least one selected from a compound (b2-1) represented by General Formula (b2-1), a compound (b3-1) represented by General Formula (b3-1), a compound (b3-2) represented by General Formula (b3-2), and a compound (b4-2) represented by General Formula (b4-2), in which, in high-performance liquid chromatography measurement, the total peak area ratio of the compound included in the compound (B) is 0.1% to 60.0% with respect to the peak area 100 of the compound (A).

Abstract: A xylylenediisocyanate composition including xylylenediisocyanate and a compound represented by Chemical Formula (1) below, wherein 0.

Abstract: In a process for producing a (poly) sulfide compound represented by General Formula (2) of the present invention, thiol compounds represented by General Formula (1) are reacted with each other in the presence of a basic compound represented by General Formula (4) or General Formula (5) and sulfur.

Abstract: A process for producing cyanonorbornene of the present invention includes Step 1 of preparing a mixture solution including 0.5% by weight to 28% by weight of methyl bicyclononadiene, with respect to a total amount of 100% by weight of dicyclopentadiene, acrylonitrile, and the methyl bicyclononadiene, in a container, and Step 2 of reacting the bicyclopentadiene with the acrylonitrile in the presence of the methyl bicyclononadiene, in the mixture solution.

Abstract: A process for producing cyanonorbornene of the present invention includes Step 1 of preparing a mixture solution including 0.5% by weight to 28% by weight of methyl bicyclononadiene, with respect to a total amount of 100% by weight of dicyclopentadiene, acrylonitrile, and the methyl bicyclononadiene, in a container, and Step 2 of reacting the bicyclopentadiene with the acrylonitrile in the presence of the methyl bicyclononadiene, in the mixture solution.

Abstract: A process for producing a pentaerythritol mercaptocarboxylic acid ester of the present invention includes: a step of reacting pentaerythritol with a mercaptocarboxylic acid, in which an absorbance of a 5 wt % aqueous solution of the pentaerythritol at a wavelength of 270 nm, which is measured using a quartz cell having an optical path length of 50 mm, is 0.07 or less.

Abstract: A xylylenediisocyanate composition including xylylenediisocyanate and a compound represented by Chemical Formula (1) below, wherein 0.

Abstract: A xylylenediisocyanate composition including xylylenediisocyanate and a compound represented by Chemical Formula (1) below, wherein 0.

Abstract: A xylylenediisocyanate composition including xylylenediisocyanate and a compound represented by Chemical Formula (1) below, wherein 0.

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 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 xylylene diisocyanate composition contains a xylylene diisocyanate and a chloromethylbenzyl isocyanate. The content ratio of the chloromethylbenzyl isocyanate is 0.2 ppm or more and below 600 ppm.

Abstract: In a process for producing a (poly) sulfide compound represented by General Formula (2) of the present invention, thiol compounds represented by General Formula (1) are reacted with each other in the presence of a basic compound represented by General Formula (4) or General Formula (5) and sulfur.

Abstract: Provided is a polymerizable composition for an optical material including (A) isocyanates having two or more isocyanato groups, which include at least an isophorone diisocyanate, (B) at least one predetermined thiol having two or more mercapto groups, (C) an acidic phosphoric acid ester represented by General Formula (1), and (D) a tin compound represented by General Formula (2), in which the acidic phosphoric acid ester (C) is contained in an amount of 0.05 parts by weight to 0.9 parts by weight, with respect to a total of 100 parts by weight of the isocyanates (A) and the thiols (B), and the tin compound (D) is contained in such an amount that the content of tin is 0.05 parts by weight to 0.3 parts by weight, with respect to a total of 100 parts by weight of the isocyanates (A) and the thiols (B).

Abstract: The polymerizable composition for an optical material of the present invention contains (A) at least one kind of isocyanate having two or more isocyanato groups, which contains aromatic isocyanate, (B) at least one kind of alcohol having two or more hydroxyl groups, (C) an acidic phosphoric acid ester represented by the following Formula (1), and (D) a benzotriazole-based compound, in which a ratio of secondary hydroxyl groups to the total molar number of primary and secondary hydroxyl groups contained in the alcohol (B) is equal to or greater than 50%, and the benzotriazole-based compound (D) is contained in an amount of 1 part by weight to 11 parts by weight with respect to a total of 100 parts by weight of the isocyanate (A) and the alcohol (B).

Abstract: A process for producing a pentaerythritol mercaptocarboxylic acid ester of the present invention includes: a step of reacting pentaerythritol with a mercaptocarboxylic acid, in which an absorbance of a 5 wt % aqueous solution of the pentaerythritol at a wavelength of 270 nm, which is measured using a quartz cell having an optical path length of 50 mm, is 0.07 or less.

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 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: The purification method of an aldehyde compound of the present invention includes a step of neutralizing a reaction solution containing an aldehyde compound by adding water and a base compound to the reaction solution, and a step of distilling the neutralized reaction solution, in which the reaction solution is obtained by reacting a compound represented by the following 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, the phosphorus compound is represented by Formula (R1O)3P, and the base compound is at least one kind selected from among carbonate and hydrogen carbonate of metals of group I on the periodic table and carbonate and hydrogen carbonate of metals of group II on the periodic table.