01 - Chemical and biological materials for industrial, scientific and agricultural use
35 - Advertising and business services
Goods & Services
(1) Non-petroleum derived chemicals used in industry, chemicals for use in manufacture of polymers, polymeric articles and personal care products, namely, specialty and industrial chemicals, namely, polymer additives for use in plastic polymers (or plasticizers); chemical esters and chemical additives used as ingredients for personal care products, namely sun care, skin care, color cosmetics, hair care and toiletry products; photo stabilizers for sunscreens; phytosterols, phytosterol esters, bisabolol and vegetal ceramides for use in skin care products; oleochemical products, namely, fatty alcohols, fatty acids, and methyl esters for emulsifiers, detackifiers, feel modifiers, solubilizers, substantivity aids, and stabilizers in skin care, sun care, color cosmetics, hair care and toiletry products; esters for use in skin care, sun care, color cosmetics, hair care and toiletry products; sodium stearate for deodorants; synthetic organic chemicals for use in the manufacture of softeners, modifiers, elasticators, and plasticizers of resinous and/or rubbery materials; non-petroleum derived chemicals, namely, plasticizers; chemical intermediaries for use in the manufacture of industrial cleaners, soil sanitizers, swimming pool water cleaning chemicals, automotive interiors, print rolls, wire, cable, film, sheet and bio-plastics; chemicals for use in the manufacture of rubbers, adhesives, caulks, sealants, inks, coatings, lubes, fluids; chemicals for use in manufacture of PVC, ABS, PET, PBT and PVB polymers; polymers for use in the manufacture of rubber belts, hoses, tires, seals, gaskets, conveyor belts and print rolls. (1) Retail, wholesale, and online sales services in the field of specialty and industrial chemicals; distribution of brochures, product catalogs, publications, technical data sheets, and material safety data sheets in the field of specialty and industrial chemicals; advertising services for others in the field of specialty and industrial chemicals, business consulting services relating to the distribution of specialty and industrial chemicals.
The present disclosure relates, according to some embodiments, to a cold process emulsifier composition comprising: at least one acrylic polymer, wherein the at least one acrylic polymer is neutralized after polymerization by at least one basic solution; a hydrophobic continuous phase comprising at least one solvent, wherein the at least one solvent has a polarity index from about 3 millinewtons per meter (mN/m) to about 30 mN/m; a hydrophilic discontinuous phase comprising water; at least one emulsifier, wherein the at least one emulsifier has a hydrophilic-lipophilic balance from about 2 to about 5; and at least one inverting agent, wherein the at least one inverting agent has a hydrophilic-lipophilic balance of at least about 10; wherein the cold process emulsifier composition is configured to form a cold process oil in water emulsion when the cold process emulsifier composition is contacted with a hydrophilic continuous phase comprising at least one aqueous solvent.
The present disclosure relates, according to some embodiments, to photostable photoactive compositions comprising (a) at least one photoactive compound that develops within itself an excited state energy when subjected to UV radiation and (b) a block copolymer comprising a plurality of blocks, wherein the block copolymer is operable to quench the excited state energy.
The present disclosure relates, according to some embodiments, to photostable UV absorbing compositions comprising para-alkoxyl phenyl substituted propenoic acid (APP) derivatives. Furthermore, the present disclosure relates to methods of prolonging the UV absorption capabilities of a composition using photostable UV absorbing compositions comprising APP derivatives.
A61K 8/81 - Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
01 - Chemical and biological materials for industrial, scientific and agricultural use
Goods & Services
Chemicals for industrial purposes; polymer modifiers used in
the manufacture of commercial, industrial and domestic
goods; chemical preparations for use in the manufacture of
personal care products.
01 - Chemical and biological materials for industrial, scientific and agricultural use
Goods & Services
Chemicals for industrial purposes; polymer modifiers used in the manufacture of commercial, industrial and domestic goods; chemical preparations for use in the manufacture of personal care products
10.
COMPOSITIONS, APPARATUS, SYSTEMS, AND METHODS FOR RESOLVING ELECTRONIC EXCITED STATES
The present disclosure relates, according to some embodiments, to molecules, including conjugated fused polycyclic molecules, that may receive excited state energy from other molecules (e.g., light-absorbing molecules) or directly from the irradiation sources. According to some embodiments, the disclosure relates to molecules, including conjugated fused polycyclic molecules, that may resolve (e.g., quench, dissipate) excited state energy, normally by way of releasing it as heat, (e.g., as heat). Conjugated fused polycyclic molecules of various structures are disclosed including Formula (III). The disclosure further relates to methods of use and/or therapy using molecules of Formulas (I), (II), and/or (III).
A method of quenching excited state energy from a photodegradable pigment that has been excited by absorption of light having a wavelength in the wavelength range of 290 - 800 nm, comprising reacting a pigment with a conjugated fused tricyclic compound having electron withdrawing groups of Formula (II) or a salt thereof: formula (II) wherein: A is selected from the group consisting of O, S, C=0, C=S, formula (III) and (IV); B1, B2, D1, and D2 are each independently selected from the group consisting of F, Cl, Br, I, CF3, CCl3, NR33+, NO2,CN, C(=O)R4, C(=O)OR1, SO2R5, aryl, and — C=CHR6; each m independently is 0, 1, 2, 3, or 4; n is 0 or 1; each R1 is independently selected from the group consisting of H, alkyl, alkenyl, alkynyl, cycloalkyl, cycloalkenyl, and aryl; R2 is selected from the group consisting of H, alkyl, cycloalkyl, alkenyl, alkynyl, and aryl; each R3 is independently selected from the group consisting of H and C1-C6 alkyl; each R4 is independently selected from the group consisting of H, alkyl, alkenyl, alkynyl, cycloalkyl, cycloalkenyl, and aryl; each R5 is independently selected from the group consisting of H, O-, OH, NH2, and CI; and, each R6 is independently selected from the group consisting of alkyl, alkenyl, alkynyl, cycloalkyl, cycloalkenyl, and aryl.
A61K 8/49 - Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds
A61K 8/40 - Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
A61K 31/382 - Heterocyclic compounds having sulfur as a ring hetero atom having six-membered rings, e.g. thioxanthenes
A61K 31/35 - Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having six-membered rings with one oxygen as the only ring hetero atom
A61K 31/277 - NitrilesIsonitriles having a ring, e.g. verapamil
A61Q 1/00 - Make-up preparationsBody powdersPreparations for removing make-up
A61Q 17/04 - Topical preparations for affording protection against sunlight or other radiationTopical sun tanning preparations
C07C 255/41 - Carboxylic acid nitriles having cyano groups bound to acyclic carbon atoms having cyano groups bound to acyclic carbon atoms of a carbon skeleton containing at least one six-membered aromatic ring the carbon skeleton being further substituted by carboxyl groups, other than cyano groups
C07C 255/34 - Carboxylic acid nitriles having cyano groups bound to acyclic carbon atoms having cyano groups bound to acyclic carbon atoms of a carbon skeleton containing at least one six-membered aromatic ring with cyano groups linked to the six-membered aromatic ring, or to the condensed ring system containing that ring, by unsaturated carbon chains
A method of reducing photodegradation of a coenzyme Q10 compound when exposed to UV radiation in a composition containing said coenzyme Q10 compound comprising combining with said coenzyme Q10 compound a compound of formula (I) in an amount effective to quench singlet excited state energy from the coenzyme Q10 compound and transfer the singlet excited state energy from the coenzyme Q10 compound to the compound of formula (I), wherein one of R1 and R2 is a straight or branched chain C1-C30alkoxy radical, and the non-alkoxy R1 or R2 is hydrogen; and R3 is a straight or branched chain C1-C30 alkyl radical, thereby photo stabilizing the retinoid compound.
01 - Chemical and biological materials for industrial, scientific and agricultural use
Goods & Services
(1) Synthetic chemicals used in industry as plasticizers or physical modifying agents to soften or otherwise physically modify natural and synthetic polymers.
14.
PHOTOSTABILIZATION OF RESVERATROL WITH ALKOXYCRYLENE COMPOUNDS
The photostabilizing electronic excited state energy - particularly singlet state energy from resveratrol compounds - has been found to be readily transferred to (accepted by) α- cyanodiphenylacrylate compounds having an alkoxy radical in the four (para) position (hereinafter "alkoxycrylenes") on one of the phenyl rings having the formula (I): wherein one of R1 and R2 is a straight or branched chain C1-C30 alkoxy radical, preferably C1-C8, more preferably methoxy, and the non-alkoxy radical R1 or R2 is hydrogen; and R3 is a straight or branched chain C1-C30 alkyl radical, preferably C2-C20. The alkoxycrylene compounds of formula (I) significantly increase the photostability of resveratrol compounds in a composition by at least 3-fold and as much as 10-fold or greater. The ability of the alkoxycrylene compounds to stabilize the resveratrol compound is concentration dependent, with the amount of resveratrol photostabilization increasing with the concentration of the alkoxycrylene compound.
The present disclosure is directed to polymer blends comprising a biopolymer and one or more impact modifiers, wherein at least one impact modifier is an ester of formula I: and to methods for increasing the impact resistance of a biopolymer with one or more impact modifiers, wherein at least one impact modifier is a ester of formula I. The polymer blends disclosed herein provide impact resistance, and are useful, for example, in the production of packaging materials, industrial products, durable goods, and the like.
The present disclosure is directed to polymer blends comprising a biopolymer and a substituted or unsubstituted aliphatic polyester. The aliphatic polyester comprises repeating units derivable from a substituted or unsubstituted aliphatic diacid, repeating units derivable from a substituted or unsubstituted aliphatic diol, and one or two terminator units derivable from a substituted or unsubstituted aliphatic alcohol. The polymer blends disclosed herein provide improved flexibility, and are useful, for example, in the production of packaging materials, industrial products, durable goods, and the like.
The present disclosure is directed to polymer blends comprising a biopolymer and a substituted or unsubstituted aliphatic polyester. The aliphatic polyester comprises repeating units derivable from a substituted or unsubstituted aliphatic diacid, repeating units derivable from a substituted or unsubstituted aliphatic diol, and one or two terminator units derivable from a substituted or unsubstituted aliphatic alcohol. The polymer blends disclosed herein provide improved flexibility, and are useful, for example, in the production of packaging materials, industrial products, durable goods, and the like.
A composition comprising an inorganic particulate material in an amount of about 20 wt% to about 70 wt%, a carrier for the particulate material comprising a compound of formula (I) in an amount of about 1 wt% to about 70 wt%, a particulate material coating material in an amount of about 0 wt% to about 5 wt%, and a dispersing agent for the particulate material in an amount of about 0 wt% to about 5 wt%, based on the total weight of the composition, Formula (I) wherein one of R1 and R2 is a straight or branched chain C1-C30 alkoxy radical, and the non- alkoxy R1 or R2 is hydrogen: and R3 is a straight or branched chain C1-C30 alkyl radical.
A61K 8/40 - Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
A61Q 17/04 - Topical preparations for affording protection against sunlight or other radiationTopical sun tanning preparations
C07C 255/41 - Carboxylic acid nitriles having cyano groups bound to acyclic carbon atoms having cyano groups bound to acyclic carbon atoms of a carbon skeleton containing at least one six-membered aromatic ring the carbon skeleton being further substituted by carboxyl groups, other than cyano groups
24.
PHOTOSTABILIZATION OF RETINOIDS WITH ALKOXYCRYLENE COMPOUNDS
The photostabilizing electronic excited state energy - particularly singlet state energy from retinoid compounds - has been found to be readily transferred to (accepted by) α-cyanodiphenylacrylate compounds having an alkoxy radical in the four (para) position (hereinafter "alkoxycrylenes") on one of the phenyl rings having the formula (I): wherein one of R1 and R2 is a straight or branched chain C1-C30 alkoxy radical, preferably C1-C8, more preferably methoxy, and the non-alkoxy radical R1 or R2 is hydrogen; and R3 is a straight or branched chain C1-C30 alkyl radical, preferably C2-C20. The alkoxycrylene compounds of formula (I) significantly increase the photostability of retinoid compounds in a composition by at least 3 -fold and as much as 10-fold or greater. The ability of the alkoxycrylene compounds to stabilize the retinoid compound is concentration dependent, with the amount of retinoid photostabilization increasing with the concentration of the alkoxycrylene compound.
A method of quenching fluorescence of a naphthalate polyester that is subjected to UV- radiation in an amount sufficient to cause the naphthalate polyester to reach an excited state and fluoresce, comprising adding to the naphthalate polyester a fluorescence quenching amount of a compound of formula (1) wherein R1 is an alkoxy, R2 is an organic linker, k is either zero or one, / is either zero or one, wherein the sum of k+l is one, and m is an integer in a range from zero to about twenty
C07C 255/41 - Carboxylic acid nitriles having cyano groups bound to acyclic carbon atoms having cyano groups bound to acyclic carbon atoms of a carbon skeleton containing at least one six-membered aromatic ring the carbon skeleton being further substituted by carboxyl groups, other than cyano groups
C08G 63/685 - Polyesters containing atoms other than carbon, hydrogen, and oxygen containing nitrogen
A61K 8/40 - Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
Polymers comprising monomers having 2-cyano-3,3-diphenyl-prop-2-enoie acid moieties having the formula are disclosed. Compositions comprising said polymers and methods for increasing the UV- absorbing, water resistance, and photostabilizing properties of compositions comprising such polymers also are disclosed.
01 - Chemical and biological materials for industrial, scientific and agricultural use
02 - Paints, varnishes, lacquers
Goods & Services
Plasticizers for PVC resins and other polymers; chemical
substances and polyurethane plastics for use in
manufacturing; chemical products for use in industry and
manufacturing processes; plastics in the form of powder,
liquids or pastes; chemical preparations containing
polyurethane elastomers; polyurethane elastomers; chemical
products for use in industry; raw materials and chemicals;
all the aforementioned goods for producing and treating
plastics materials. Paints, varnishes, lacquers; preservatives against rusts and
against deterioration of wood; colorants; mordants; raw
natural resins; metals in foil and powder form for painters,
decorators, printers and artists; ceramic paints; coatings.
01 - Chemical and biological materials for industrial, scientific and agricultural use
02 - Paints, varnishes, lacquers
04 - Industrial oils and greases; lubricants; fuels
Goods & Services
Chemicals used in industry, including synthetic resinous materials and solutions thereof; coating materials and compounds; artificial and synthetic resins, artificial and synthetic resinous compounds and compounds principally of synthetic resins; (unprocessed) plastics, including (unprocessed) plastics in the form of powders, pastes, liquids, emulsions, dispersions or granulates for use in industry; chemical additives, including plasticizers and softeners, including plasticizers for synthetic resins and polymers; synthetic resins including embedding resins and synthetic resin mixtures, not intended for oil additives and products made therefrom; artificial and synthetic resins and synthetic resinous compounds, also in the form of powders, liquids, pastes, emulsions, dispersions or granules for industrial use and for use in the manufacture of coatings and as plasticizers for use in the plastics industry; molding compounds, embedding resins and (other) chemical substances, including such goods for use in forming, molding or casting shaped articles; injection molding compounds; viscous, resinous or rubber-like condensation products or solutions thereof used in the production of nitrocellulose lacquers, plastics, plastic coatings and similar products; synthetic resinous polyester-type condensation products and their solutions, suitable for use as plasticizers or modifiers for coverings for surfaces, plastic products, cellulose and polyvinyl resins; all products in class 1. Synthetic resinous materials and their solutions to be mainly used in pigmented form or not, as protective coatings. Industrial oils and greases; epoxidized vegetable oils used on plasticizers for chloride polyvinyl and other synthetic materials.
01 - Chemical and biological materials for industrial, scientific and agricultural use
04 - Industrial oils and greases; lubricants; fuels
16 - Paper, cardboard and goods made from these materials
Goods & Services
Chemicals used in industry; chemicals and chemical preparations used in and for lubricants, lubricating oils and lubricating fluids. Industrial oils and greases; lubricants; lubricating oils and lubricating fluids. Printed materials, namely brochures, product catalogs, publications, technical data sheets and material safety data sheets in the field of chemicals.
A silicone fluid comprising a chromophore-substituted polyorganosiloxane having a formula (2) wherein x is an integer in the range of 60 to 2000, \ is an integer in the range of 5 to 100, a ratio \ y is in a range of about 10 1 to about 20 1, and X is a photostabilizing chromophore
A method of testing a compound for its capability of quenching singlet excited state energy from a photon-excited photoactive compound, thereby photostabilizing said photoactive compound, comprising mixing: (1) a composition comprising a photoactive compound in a solvent and determining the degree of fluorescence of said composition (1) by exposing the composition (1) to UV radiation in an amount sufficient for the photoactive compound to reach an electronic singlet excited state, and (2) a mixture comprising said photoactive compound with a test compound in a solvent, and determining the degree of fluorescence of said mixture (2) by exposing the mixture to UV radiation to the same degree as composition (1), and comparing the degree of fluorescence of composition (1) with mixture (2).
Disclosed herein are compounds of formula (I), compositions having compounds of formula (I) and methods of stabilizing a photodegradable polymer or compound in a composition; wherein R1, R2, and R3 are the same or different and are selected from the group consisting of C1 -C30 alkyl, C3-C8 cycloalkyl, substituted alkyl, substituted cycloalkyl, ester, aryl, heteroaryl, heterocycloalkyl, substituted aryl, substituted heteroaryl, substituted heterocycloalkyl, and amino; R4, R5, R6, and R7 are each independently selected from the group consisting of hydrogen and alkoxy, wherein R4 and R5 cannot both be hydrogen and R6 and R7 cannot both be hydrogen; a, b, c, and d are each independently an integer of 1 to 4; n is an integer of 1 to 100; and s is an integer of 0 to 100.
C07C 255/41 - Carboxylic acid nitriles having cyano groups bound to acyclic carbon atoms having cyano groups bound to acyclic carbon atoms of a carbon skeleton containing at least one six-membered aromatic ring the carbon skeleton being further substituted by carboxyl groups, other than cyano groups
C08G 63/00 - Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
C08L 67/00 - Compositions of polyesters obtained by reactions forming a carboxylic ester link in the main chainCompositions of derivatives of such polymers
The photostabilizing electronic excited state energy - particularly singlet state energy from a UV-absorbing molecule has been found to be readily transferred to (accepted by) α-cyanodiphenylacrylate compounds of formulas (I) and (V) having an alkoxy radical preferably in the four (para) position (hereinafter methoxycrylenes) on one or both of the phenyl rings: (I) wherein at least one of R1 and R2 is a straight or branched chain C1 -C 12 alkoxy radical, preferably C1-C8, more preferably C1-C4, and most preferably methoxy, and any non-alkoxy radical R1 or R2 is hydrogen; and R3 is a straight or branched chain C1 -C24 alkyl radical, preferably C12-C24, more preferably C2O (II); wherein A and B are the same or different and are selected from the group consisting of oxygen, amino and sulfur; R1 and R3 are the same or different and are selected from the group consisting Of C1-C3O alkyl, C2-C30 alkylene, C2-C3O alkyne, C3-C8 cycloalkyl, C1-C3O substituted alkylene, C2-C3O substituted alkyne, aryl, substituted aryl, heteroaryl, heterocycloalkyl, substituted heteroaryl and substituted heterocycloalkyl; R2 is selected from the group consisting Of C1-C3O alkyl, C2-C3O alkylene, C2C30 alkyne, C3-C8 cycloalkyl, C1-C30 substituted alkyl, C3-C8 substituted cycloalkyl, C1-C30 substituted alkylene, C2-C3O substituted alkyne; R4, R5, R6 and R7 are the same or different and are selected from the group consisting of C1-C3O alkoxy straight chin on branched and a, b, c and d are each either 0 or 1, and a, b, c and d add up to 1, 2, 3, or 4.
A61K 8/40 - Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
A61Q 17/04 - Topical preparations for affording protection against sunlight or other radiationTopical sun tanning preparations
C07C 255/41 - Carboxylic acid nitriles having cyano groups bound to acyclic carbon atoms having cyano groups bound to acyclic carbon atoms of a carbon skeleton containing at least one six-membered aromatic ring the carbon skeleton being further substituted by carboxyl groups, other than cyano groups
35.
METHOD OF QUENCHING ELECTRONIC EXCITATION OF CHROMOPHORE-CONTAINING ORGANIC MOLECULES IN PHOTOACTIVE COMPOSITIONS
The photostabilizing electronic excited state energy - particularly singlet state energy from a UV-absorbing molecule has been found to be readily transferred to (accepted by) α-cyanodiphenylacrylate compounds of formulas (I) and (V) having an alkoxy radical preferably in the four (para) position (hereinafter methoxy crylenes) on one or both of the phenyl rings: wherein at least one of R1 and R2 is a straight or branched chain C1-C12 alkoxy radical, preferably C1-C8, more preferably C1 -C4, and most preferably methoxy, and any non-alkoxy radical R1 or R2 is hydrogen; and R3 is a straight or branched chain C1-C24 alkyl radical, preferably C12-C24, more preferably C20; wherein A and B are the same or different and are selected from the group consisting of oxygen, amino and sulfur; R1 and R3 are the same or different and are selected from the group consisting of C1-C3O alkyl, C2-C3O alkylene, C2-C3O alkyne, C3-C8 cycloalkyl, C1-C3O substituted alkylene, C2-C3O substituted alkyne, aryl, substituted aryl, heteroaryl, heterocycloalkyl, substituted heteroaryl and substituted heterocycloalkyl; R2 is selected from the group consisting of C1-C3O alkyl, C2-C3O alkylene, C2C30 alkyne, C3-C8 cycloalkyl, C1-C3O substituted alkyl, C3-C8 substituted cycloalkyl, C1-C3O substituted alkylene, C2-C3O substituted alkyne; R4, R5, R6 and R7 are the same or different and are selected from the group consisting of C1-C3O alkoxy straight chin on branched and a, b, c and d are each either 0 or 1, and a, b, c and d add up to 1, 2, 3, or 4.
A61K 8/40 - Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
A61Q 17/04 - Topical preparations for affording protection against sunlight or other radiationTopical sun tanning preparations
C07C 255/41 - Carboxylic acid nitriles having cyano groups bound to acyclic carbon atoms having cyano groups bound to acyclic carbon atoms of a carbon skeleton containing at least one six-membered aromatic ring the carbon skeleton being further substituted by carboxyl groups, other than cyano groups
01 - Chemical and biological materials for industrial, scientific and agricultural use
16 - Paper, cardboard and goods made from these materials
35 - Advertising and business services
Goods & Services
Chemicals used in industry, science and photography; unprocessed artificial resins, unprocessed plastics; manures; fire extinguishing compositions; tempering and soldering preparations; chemical substances for preserving foodstuffs; tanning substances; adhesives used in industry; magnesium oxide; chemical compounds for industrial use; mineral raw materials. Product specification sheets, instruction manuals, catalogs in the field of chemicals. Retail and wholesale sales and consulting services in the field of chemicals.
01 - Chemical and biological materials for industrial, scientific and agricultural use
16 - Paper, cardboard and goods made from these materials
35 - Advertising and business services
Goods & Services
Speciality and industrial chemicals. Printed materials, namely brochures, product catalogs, publications, technical data sheets and material safety data sheets in the field of speciality and industrial chemicals. Retail, wholesale and online sales services in the field of speciality and industrial chemicals; distribution of brochures, product catalogs, publications, technical data sheets and material safety data sheets in the field of speciality and industrial chemicals; advertising services for others in the field of speciality and industrial chemicals, business consulting services relating to distribution of speciality and industrial chemicals.
01 - Chemical and biological materials for industrial, scientific and agricultural use
16 - Paper, cardboard and goods made from these materials
35 - Advertising and business services
Goods & Services
(1) Non-petroleum derived chemicals used in industry, chemicals for use in manufacture of polymers, polymeric articles and personal care products, namely, specialty and industrial chemicals, namely, polymer additives for use in plastic polymers (or plasticizers); chemical esters and chemical additives used as ingredients for personal care products, namely sun care, skin care, color cosmetics, hair care and toiletry products; photo stabilizers for sunscreens; phytosterols, phytosterol esters, bisabolol and vegetal ceramides for use in skin care products; oleochemical products, namely, fatty alcohols, fatty acids, and methyl esters for emulsifiers, detackifiers, feel modifiers, solubilizers, substantivity aids, and stabilizers in skin care, sun care, color cosmetics, hair care and toiletry products; esters for use in skin care, sun care, color cosmetics, hair care and toiletry products; sodium stearate for deodorants; synthetic organic chemicals for use in the manufacture of softeners, modifiers, elasticators, and plasticizers of resinous and/or rubbery materials; non- petroleum derived chemicals, namely, plasticizers; chemical intermediaries for use in the manufacture of industrial cleaners, soil sanitizers, swimming pool water cleaning chemicals, automotive interiors, print rolls, wire, cable, film, sheet and bio-plastics; chemicals for use in the manufacture of rubbers, adhesives, caulks, sealants, inks, coatings, lubes, fluids; chemicals for use in manufacture of PVC, ABS, PET, PBT and PVB polymers; polymers for use in the manufacture of rubber belts, hoses, tires, seals, gaskets, conveyor belts and print rolls.
(2) Printed materials, namely brochures, product catalogs, publications, technical data sheets and material safety data sheets in the field of specialty and industrial chemicals. (1) Retail, wholesale and online sales services in the field of specialty and industrial chemicals; distribution of brochures, product catalogs, publications, technical data sheets and material safety data sheets in the field of specialty and industrial chemicals; advertising services for others in the field of specialty and industrial chemicals, business consulting services relating to distribution of specialty and industrial chemicals.
01 - Chemical and biological materials for industrial, scientific and agricultural use
Goods & Services
Chemicals for industrial purposes; polymer modifiers used in the manufacture of commercial, industrial and domestic goods; chemical preparations for use in the manufacture of personal care products
01 - Chemical and biological materials for industrial, scientific and agricultural use
Goods & Services
(1) Non-petroleum derived chemicals, namely plasticizers; plasticizers of resinous and/or rubbery materials for use in the manufacture of softeners, modifiers, elasticators.
(2) Chemicals for use in manufacture of polymers, polymeric articles and personal care products, namely, specialty and industrial chemicals, namely, polymer additives for use in plastic polymers (or plasticizers); chemical esters and chemical additives used as ingredients for personal care products, namely sun care, skin care, color cosmetics, hair care and toiletry products; photo stabilizers for sunscreens; phytosterols, phytosterol esters, bisabolol and vegetal ceramides for use in skin care products; oleochemical products, namely, fatty alcohols, fatty acids, and methyl esters for emulsifiers, detackifiers, feel modifiers, solubilizers, substantivity aids, and stabilizers in skin care, sun care, color cosmetics, hair care and toiletry products; esters for use in skin care, sun care, color cosmetics, hair care and toiletry products; sodium stearate for deodorants; synthetic organic chemicals for use in the manufacture of softeners, modifiers, elasticators, chemical intermediaries for use in the manufacture of industrial cleaners, soil sanitizers, swimming pool water cleaning chemicals, automotive interiors, print rolls, wire, cable, film, sheet and bio-plastics; chemicals for use in the manufacture of rubbers, adhesives, caulks, sealants, inks, coatings, lubes, fluids; chemicals for use in manufacture of PVC, ABS, PET, PBT and PVB polymers; polymers for use in the manufacture of rubber belts, hoses, tires, seals, gaskets, conveyor belts and print rolls.
01 - Chemical and biological materials for industrial, scientific and agricultural use
16 - Paper, cardboard and goods made from these materials
35 - Advertising and business services
Goods & Services
Specialty chemicals not included in other classes; industrial chemicals. Printed materials, namely brochures, product catalogs, publications, technical data sheets and material safety data sheets in the field of specialty and industrial chemicals. Retail, wholesale and online sales services in the field of specialty and industrial chemicals; distribution of brochures, product catalogs and promotional publcations; distribution of informational publications including technical data sheets and material safety data sheets in the field of specialty and industrial chemicals; advertising services for others in the field of specialty and industrial chemicals, business consulting services relating to distribution of specialty and industrial chemicals.
01 - Chemical and biological materials for industrial, scientific and agricultural use
Goods & Services
Chemicals for industrial purposes; polymer modifiers used in the manufacture of commercial, industrial and domestic goods; chemical preparations for use in the manufacture of personal care products
01 - Chemical and biological materials for industrial, scientific and agricultural use
Goods & Services
Plasticizers for PVC resins and other polymers; chemical substances included in Class 1, namely plasticizers for PVC resins and other polymers, all for use in manufacturing; chemical products for use in industry and manufacturing processes, namely plasticizers for PVC resins and other polymers; chemical products for use in industry, namely plasticizers for PVC resins and other polymers; raw materials and chemicals, namely plasticizers for PVC resins and other polymers; all the aforementioned goods in Class 1 for producing and treating plastics materials.
01 - Chemical and biological materials for industrial, scientific and agricultural use
Goods & Services
Ultraviolet radiation-absorbing chemical compounds for use in industry in the manufacture of a wide variety of goods, including the manufacture of cosmetics and topically applied personal care products
01 - Chemical and biological materials for industrial, scientific and agricultural use
Goods & Services
synthetic chemicals used in industry as plasticizers or physical modifying agents to soften or otherwise physically modify natural and synthetic polymers
01 - Chemical and biological materials for industrial, scientific and agricultural use
Goods & Services
VISCOUS, RESINOUS, OR RUBBER-LIKE CONDENSATION PRODUCT OR SOLUTION THEREOF USED IN THE PRODUCTION OF NITROCELLULOSE LACQUERS, PLASTICS, AND OTHER TYPES OF COATINGS
