A61Q3/02

TRANSPARENT BOTTLE WITH UV COATING FOR UV NAIL GEL COMPOSITIONS, SYSTEMS AND METHODS
20220192343 · 2022-06-23 · ·

A UV nail gel and clear bottle system and method for protecting the ultraviolet (UV) nail gel formulation from curing or gelling while providing visibility of the UV nail gel formula. The system includes one or more layer of a transparent UV blocking treatment located on an exterior surface of the clear bottle comprising one or more UV absorber having an intramolecular hydrogen bond and absorption wavelengths ranging from 100 nanometers to 380 nanometers, paired with a UV nail gel formula comprising a lower curing photoinitiator having an absorption wavelength≤330 nm. The one or more layer of the transparent UV blocking treatment and UV nail gel formula with the lower curing photoinitiator protects the UV nail gel formulation from curing or gelling while providing visibility of the UV nail gel formula.

TRANSPARENT BOTTLE WITH UV COATING FOR UV NAIL GEL COMPOSITIONS, SYSTEMS AND METHODS
20220192343 · 2022-06-23 · ·

A UV nail gel and clear bottle system and method for protecting the ultraviolet (UV) nail gel formulation from curing or gelling while providing visibility of the UV nail gel formula. The system includes one or more layer of a transparent UV blocking treatment located on an exterior surface of the clear bottle comprising one or more UV absorber having an intramolecular hydrogen bond and absorption wavelengths ranging from 100 nanometers to 380 nanometers, paired with a UV nail gel formula comprising a lower curing photoinitiator having an absorption wavelength≤330 nm. The one or more layer of the transparent UV blocking treatment and UV nail gel formula with the lower curing photoinitiator protects the UV nail gel formulation from curing or gelling while providing visibility of the UV nail gel formula.

Diester cosmetic formulations and uses thereof
11357714 · 2022-06-14 · ·

The present application relates to compounds, formulations, kits and methods of use in the cosmetics field. A cosmetic formulation comprising a diester compound of Formula (I) or Formula (II), or a combination thereof, and one or more cosmetically acceptable carriers or excipients. The structures of compounds of Formula (I) and Formula (II) are shown below: ##STR00001##

Diester cosmetic formulations and uses thereof
11357714 · 2022-06-14 · ·

The present application relates to compounds, formulations, kits and methods of use in the cosmetics field. A cosmetic formulation comprising a diester compound of Formula (I) or Formula (II), or a combination thereof, and one or more cosmetically acceptable carriers or excipients. The structures of compounds of Formula (I) and Formula (II) are shown below: ##STR00001##

PHOTOCURABLE RESIN COMPOSITION FOR NAIL OR ARTIFICIAL NAIL, CURED PRODUCT, AND METHOD FOR COATING NAIL OR ARTIFICIAL NAIL
20230270659 · 2023-08-31 ·

A photocurable resin composition for a nail or an artificial nail can form a cured product that has excellent transparency and gloss while having hardness required for coating a nail or an artificial nail. The photocurable resin composition for a nail or an artificial nail contains components (A) to (D): component (A): a urethane (meth)acrylate oligomer, component (B): a compound having three or more (meth)acryloyl functional groups (excluding the component (A)), component (C): a compound having a molecular weight of 200 or less and having a hydroxyl group and a methacryloyl group (excluding the components (A) and (B)), and component (D): a photoinitiator.

PHOTOCURABLE RESIN COMPOSITION FOR NAIL OR ARTIFICIAL NAIL, CURED PRODUCT, AND METHOD FOR COATING NAIL OR ARTIFICIAL NAIL
20230270659 · 2023-08-31 ·

A photocurable resin composition for a nail or an artificial nail can form a cured product that has excellent transparency and gloss while having hardness required for coating a nail or an artificial nail. The photocurable resin composition for a nail or an artificial nail contains components (A) to (D): component (A): a urethane (meth)acrylate oligomer, component (B): a compound having three or more (meth)acryloyl functional groups (excluding the component (A)), component (C): a compound having a molecular weight of 200 or less and having a hydroxyl group and a methacryloyl group (excluding the components (A) and (B)), and component (D): a photoinitiator.

COSMETIC OR PERSONAL CARE FORMULATIONS CONTAINING POROUS METAL OXIDE SPHERES

A cosmetic or personal care formulation includes a carrier and porous metal oxide spheres wherein, the porous metal oxide spheres have, e.g., an average diameter of about 0.5 μm to about 100 μm and an average porosity of about 0.10 to about 0.80; the porous metal oxide spheres have one or more population of pores each having an average pore diameter, wherein each population has a different average pore diameter and wherein the average pore diameters are, e.g., from about 50 nm to about 999 nm.

COSMETIC OR PERSONAL CARE FORMULATIONS CONTAINING POROUS METAL OXIDE SPHERES

A cosmetic or personal care formulation includes a carrier and porous metal oxide spheres wherein, the porous metal oxide spheres have, e.g., an average diameter of about 0.5 μm to about 100 μm and an average porosity of about 0.10 to about 0.80; the porous metal oxide spheres have one or more population of pores each having an average pore diameter, wherein each population has a different average pore diameter and wherein the average pore diameters are, e.g., from about 50 nm to about 999 nm.

Crosslinkable coating compositions formulated with dormant carbamate initiator

A crosslinkable coating composition comprising: ingredient A that has at least two protons that can be activated to form a Michael carbanion donor; ingredient B that functions as a Michael acceptor having at least two ethylenically unsaturated functionalities each activated by an electron-withdrawing group; and a dormant carbamate initiator of Formula (1) ##STR00001##
wherein R.sub.1 and R.sub.2 can be independently selected from hydrogen, a linear or branched substituted or unsubstituted alkyl group having 1 to 22 carbon atoms; 1 to 8 carbon atoms; and A.sup.n+ is a cationic species or polymer and n is an integer equal or greater than 1 with the proviso that A.sup.n+ is not an acidic hydrogen; and optionally further comprising ammonium carbamate (H.sub.2NR.sub.1R.sub.2.sup.+−OC═ONR.sub.1R.sub.2). The crosslinkable coating composition can be used for a variety of coating applications including nail coating compositions.

Crosslinkable coating compositions formulated with dormant carbamate initiator

A crosslinkable coating composition comprising: ingredient A that has at least two protons that can be activated to form a Michael carbanion donor; ingredient B that functions as a Michael acceptor having at least two ethylenically unsaturated functionalities each activated by an electron-withdrawing group; and a dormant carbamate initiator of Formula (1) ##STR00001##
wherein R.sub.1 and R.sub.2 can be independently selected from hydrogen, a linear or branched substituted or unsubstituted alkyl group having 1 to 22 carbon atoms; 1 to 8 carbon atoms; and A.sup.n+ is a cationic species or polymer and n is an integer equal or greater than 1 with the proviso that A.sup.n+ is not an acidic hydrogen; and optionally further comprising ammonium carbamate (H.sub.2NR.sub.1R.sub.2.sup.+−OC═ONR.sub.1R.sub.2). The crosslinkable coating composition can be used for a variety of coating applications including nail coating compositions.