Provided is an eyelash extension adhesive comprising the following components (a) and (b): (a) a monofunctional monomer of formula (I) wherein R.sup.1 represents a hydrogen atom or a methyl group, and R.sup.2 to R.sup.6 each independently represent a hydrogen atom or a C1 to C6 alkyl group, and (b) a photopolymerization initiator. The eyelash extension adhesive is excellent in durability and water resistance, can adhere easily to eyelashes even in a wet state, and is very useful as a photopolymerizable adhesive for eyelash extension attachment not including a cyanoacrylate compound.

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Provided is an eyelash extension adhesive comprising the following components (a) and (b): (a) a monofunctional monomer of formula (I) wherein R.sup.1 represents a hydrogen atom or a methyl group, and R.sup.2 to R.sup.6 each independently represent a hydrogen atom or a C1 to C6 alkyl group, and (b) a photopolymerization initiator. The eyelash extension adhesive is excellent in durability and water resistance, can adhere easily to eyelashes even in a wet state, and is very useful as a photopolymerizable adhesive for eyelash extension attachment not including a cyanoacrylate compound.

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Provided are a photocurable material composition providing a cured product, which achieves both of a heat deflection temperature of 70° C. or more measured by Method A of JIS K 7191-1 and a Charpy impact strength of 6 kJ/m.sup.2 or more measured in conformity with JIS K 7111-1, after UV irradiation, and a cured product thereof. The photocurable material composition includes: 50 parts by weight to 65 parts by weight of a bifunctional urethane (meth)acrylate having (meth)acryloyl groups at both terminals thereof; 15 parts by weight to 25 parts by weight of a compound represented by the formula (4); and 10 parts by weight to 30 parts by weight of at least one of a compound represented by the formula (5) or a compound represented by the formula (6).

Provided are a photocurable material composition providing a cured product, which achieves both of a heat deflection temperature of 70° C. or more measured by Method A of JIS K 7191-1 and a Charpy impact strength of 6 kJ/m.sup.2 or more measured in conformity with JIS K 7111-1, after UV irradiation, and a cured product thereof. The photocurable material composition includes: 50 parts by weight to 65 parts by weight of a bifunctional urethane (meth)acrylate having (meth)acryloyl groups at both terminals thereof; 15 parts by weight to 25 parts by weight of a compound represented by the formula (4); and 10 parts by weight to 30 parts by weight of at least one of a compound represented by the formula (5) or a compound represented by the formula (6).

The present disclosure provides a biodegradable super absorbent polymer including a crosslinked polymer of a monomer including a modified polysaccharide having a maleic acid group (—OCOCH═CHCOOH) and a sulfosuccinic acid group (—OCOCH(SO.sub.3H)CH.sub.2COOH), which exhibits excellent biodegradability without deterioration in physical properties of the super absorbent polymer such as centrifuge retention capacity and absorbency under pressure, and a method for producing the same.

The present disclosure provides a biodegradable super absorbent polymer including a crosslinked polymer of a monomer including a modified polysaccharide having a maleic acid group (—OCOCH═CHCOOH) and a sulfosuccinic acid group (—OCOCH(SO.sub.3H)CH.sub.2COOH), which exhibits excellent biodegradability without deterioration in physical properties of the super absorbent polymer such as centrifuge retention capacity and absorbency under pressure, and a method for producing the same.

An active energy ray curable composition contains an acrylamide compound A1 represented by the following Chemical formula 1 or the following Chemical formula 2; a multi-functional polymerizable compound B1 having an SI value of 3 or less in a skin sensitivity test; a polymerization initiator C1 having no maximum absorption peak in a wavelength range of from 365 to 405 nm; and a hydrogen donor D, ##STR00001##

An active energy ray curable composition contains an acrylamide compound A1 represented by the following Chemical formula 1 or the following Chemical formula 2; a multi-functional polymerizable compound B1 having an SI value of 3 or less in a skin sensitivity test; a polymerization initiator C1 having no maximum absorption peak in a wavelength range of from 365 to 405 nm; and a hydrogen donor D, ##STR00001##

Provided are a photosensitive composition including a coloring material A including a pigment, a pigment derivative B, and a dispersant C, in which the pigment derivative B includes a pigment derivative B1 in which a maximum value of a molar absorption coefficient in a wavelength range of 400 to 700 nm is 3000 L.Math.mol.sup.−1.Math.cm.sup.−1 or less, the dispersant C includes a dispersant C1 having an ethylenically unsaturated bond-containing group, and a total content of the coloring material A and the pigment derivative B in a total solid content of the photosensitive composition is 50% by mass or more; a film formed of the photosensitive composition; an optical filter, a solid-state imaging element; and an image display device.

Provided are a photosensitive composition including a coloring material A including a pigment, a pigment derivative B, and a dispersant C, in which the pigment derivative B includes a pigment derivative B1 in which a maximum value of a molar absorption coefficient in a wavelength range of 400 to 700 nm is 3000 L.Math.mol.sup.−1.Math.cm.sup.−1 or less, the dispersant C includes a dispersant C1 having an ethylenically unsaturated bond-containing group, and a total content of the coloring material A and the pigment derivative B in a total solid content of the photosensitive composition is 50% by mass or more; a film formed of the photosensitive composition; an optical filter, a solid-state imaging element; and an image display device.