762 results about "Stearyl alcohol" patented technology

The present invention provides stable aerosol cream mousse composition, preferably hair care composition, that can provide enhanced touch, combability, alignment and volume reduction to the hair, with low or reduced greasy, oily hair feel, while being formulated having a thick, rich, creamy, mousse-type rheology with excellent spreading, perception of spreading, and feel. The aerosol composition is based on the combination of component (A) a cationic surfactant, which is generally a quaternary ammonium compound such as e.g., ditallow dimethyl ammonium chloride; (B) a fatty alcohol, such as cetyl and stearyl alcohol; and (C) carbon dioxide.

Extrusion of a mix containing a pharmaceutically active agent can be achieved using a plasticising excipient in an amount sufficient to act as plasticiser and also act as lubricant, thereby avoiding the need for inclusion of a lubricant. The invention provides multiparticulates with controlled release properties, substantially free of lubricant. The present invention is preferably directed to extruded multiparticulates containing an opioid such as oxycodone, an ammonium methacrylate copolymer such as Eudragit® RSPO, a plasticising excipient such as preferably stearyl alcohol and a water permeability modifier such as preferably Eudragit® RLPO. The obtained multiparticulates show a release rate profile which is pH-independent.

Disclosed is a topical skin care composition that includes water, silymarin, hydrolyzed algin, palmitoyl tripeptide 8, ceramide 2, pomegranate extract comprising pomegranate sterols, glycerin, disodium EDTA, caprylic/capric triglyceride, shea butter, C12-15 alcohols benzoate, dimethicone, glyceryl stearate and PEG 100 stearate, cetyl alcohol, stearyl alcohol, stearic acid, butylene glycol, caprylyl glycol, and (s) a mixture of acrylamide/sodium acryloyldimethyl taurate copolymer, isohexadecane, and polysorbate 80.

The present invention relates to a composition used as a vehicle for percutaneous absorption of Pharmaceutical and Cosmaceutical active agents that comprises Dimethiconol (hydroxyl-terminated polydimethydimethylsiloxane), dimethicone-350 (polydimethylsiloxane-350), cyclomethicone-5 nf (decamethylcyclopentasiloxane), alkymeth siloxane copolyol-lauryl peg/ppg 18/18 methicone (alkymethyl siloxane copolyol), cyclopentasiloxane and dimethicone Crosspolymer (silicone elastomer and decamethylcyclopentasiloxane), stearoxytrimethylsilane and stearyl alcohol (silicone wax), and deionized water. This composition serves several key applications: (1) it is a vehicle for percutaneous absorption of Pharmaceutical and Cosmaceutical active agents; (2) it acts as a method for utilizing other compositions in the treatment of inflammatory conditions of the skin including, but by no means limited to, atopic dermatitis (eczema), allergic contact dermatitis, seborrheic dermatitits, psoriasis, xerosis and atopia; (3) it is a treatment of inflammatory conditions of mucosae; (4) it relates to other compositions and methods for protecting and enhancing the barrier function of the skin.

The invention comprises a formulation for a semi-hard stick-type dentifrice optimally for use in an oral hygiene device which utilizes such semi-hard stick-type dentifrice, most often used when traveling. The dentifrice includes a primary base material such as glycerin. Sodium benzoate is included as a preservative. Sodium coco-sulfate and a mixture of wheat gluten proteins and potassium cocoate provide a foaming material. Cleansers are included and the dentifrice is strengthened by vegetal-based sodium stearate and vegetal-based stearyl alcohol. Whitening materials are included, as is an absorption material and sodium bicarbonate as an abrasive.

The invention relates to new self-emulsifying preparations containing (a) 7 to 20% by weight stearyl oligoglycoside, (b) 7 to 20% by weight cetyl oligoglycoside, (c) 0.1 to 3% by weight myristyl oligoglycoside, (d) 0.5 to 7% by weight lauryl oligoglycoside, (e) 4 to 12% by weight cetyl alcohol, (f) 10 to 20% by weight stearyl alcohol,

• (g) 20 to 30% by weight C_16/18 partial glycerides containing 58 to 62% by weight monoglyceride and
• (h) 20 to 30% by weight C_16/18 partial glycerides containing 30 to 45% by weight monoglyceride, with the proviso that the quantities shown add up to 100% by weight with water.

Disclosed are antiperspirant stick compositions that exhibit substantially less visible residue (whitening) upon application to the skin or after drying and which exhibit improved aesthetics and superior cosmetic properties. The compositions include a non-liquid organic ester emollient with a melting point between about 25° C. and about 60° C. (preferably isostearyl behenate); and an inert polymeric material (preferably a low molecular weight polyethylene; in addition to (a) a volatile (for example, cyclomethicone), (b) a non-volatile liquid emollient; (c) a gelling agent (for example, stearyl alcohol and hydrogenated castor oil); (d) at least one active antiperspirant material (for example, particulate antiperspirant aluminum zirconium tetrachlorohydrex salts); and (e) optionally other antiperspirant stick compatible materials.

The invention discloses an acne removing and antiallergic cream which is prepared by mixing stearyl alcohol polyether-2, stearyl alcohol polyether-20, glycerin stearate, PEG (Polyethylene Glycol)-100 stearate, stearic acid, cetearyl alcohol, aloe oil, polydimethyl siloxane, isopropyl myristate, propyl p-hydroxybenzoate, methyl p-hydroxybenzene, tocopherol, azone, bisabolol, glycerol, xanthan gum, EDTA (Ethylene Diamine Tetraacetic Acid)-2Na, propylene glycol, ethanol, menthol, salicylic acid, a golden cypress extractive, a scutellaria baicalensis extractive, an India chinaberry leaf extractive, a spiraea ulmaria extractive, a bee milk extractive, an aloe leaf extractive, tea tree oil and sodium hydroxide. The acne removing and antiallergic cream disclosed by the invention can be used for removing acnes, promoting the facial blood circulation and skin cell regeneration, improving the skin tolerance and reducing or eliminating the allergic reaction of the skin; the allergic tolerance of the skin is improved, so that the cream is safe and effective; no any spices are added, so that allergens are greatly reduced.

The invention discloses a low-temperature soaping agent for reactive dyes, belonging to the soaping process of the printing and dyeing industry. The low-temperature soaping agent is formed by compounding high-efficiency surfactant and auxiliaries, and comprises the following components in percentage by weight: 5-20wt% of stearyl alcohol polyether, 10-60wt% of anion- nonionic surfactant, 1-10wt% of sodium carboxymethyl cellulose (CMC), 0.1-5wt% of polyvinylpyrrolidone (PVP), 0.1-5wt% of sodium polyacrylate (PAAS), 1-20wt% of triethanolamine (TEA), and the balance being water. The soaping agent is free of phosphor, alkylphenol polyoxyethylene ether and harmful solvent, can be biodegradable, has low foaming performance and self-chelating performance, is used for soaping reactive dyes after dyeing, has a good soaping effect at a soaping temperature of 60 DEG C, and can save energy and reduce consumption.

The invention relates to a bamboo weaving softening agent and a preparation method thereof. The preparation method comprises the following steps: putting glycerol, alcohol ether glucoside, polyethenoxy ether and a surfactant into a stirring tank, stirring for 30 minutes at 80 DEG C, adding glyoxal, formaldehyde and ammonium persulfate, simultaneously adding talcum powder, limestone flour and calcium carbonate, quickly stirring at 130 DEG C for 3 minutes, finally adding stearyl alcohol, stearic acid, ethyl carbamate and paraffin, stirring for 1 hour, and cooling to normal temperature. The softening agent prepared by the method has the advantages of favorable softening effect, no corrosion and better effects, enhances the strength and toughness of the softened part, and is convenient for popularization and use.

The invention discloses a tilmicosin solid dispersible granule as well as a preparation method and an application thereof. The tilmicosin solid dispersible granule consists of tilmicosin and a carrier accessory. The carrier accessory is one of glycerin monostearate, stearyl alcohol, saturated triglyceride, glycerinum simple lipid, paraffin wax, animal wax, vegetable wax or fatty powder or mixture thereof. The preparation method of the tilicosin solid dispersible granule comprises the following steps: weighing respective carrier accessories according to the formula proportion, heating, melting and mixing uniformly; adding the tilmicosin, stirring uniformly, cooling, pelleting through spraying of a fluidized bed, balling, cooling, sieving and collecting to obtain the tilmicosin solid dispersible granule. The tilmicosin solid dispersible granule solves the problem of medicine palatability, by feed mixing administration, the fluidity and dispersibility are good and medication is convenient; after animals take the granule, the medicine releases slowly, so that the safety is high; besides, the biological availability of tilmicosin medicine is enhanced, and the clinical using effect is remarkable.

The invention relates to an enteric-coated tilmicosin slow-release micro-capsule preparation and a preparation method thereof and belongs to the field of tilmicosin preparations. The enteric-coated tilmicosin slow-release micro-capsule preparation provided by the invention comprises an inner core layer and a coating layer, wherein the inner core layer comprises tilmicosin raw powder and an auxiliary material; the auxiliary material comprises one or more than one of stearic acid, glycerin monostearate, stearyl alcohol, saturated triglyceride, monoglyceride and paraffin; and the coating layer is made from one or more than one of cellulose acetate phthalate, hydroxypropyl methyl cellulose phthalate, acrylic resin, polyvinyl acetate phthalate and acetic hydroxypropyl methylcellulose succinate. The preparation method comprises the following steps of: carrying out primary coating on the tilmicosin raw powder and the auxiliary material, carrying out secondary coating by using the materials of the coating layer, and drying to obtain the finished product. According to the invention, the tilmicosin is coated by using high polymer materials and the coated tilmicosin micro-capsule is undissolved in acid environment and slowly dissolved in alkaline environment of enteric canal, so that the purpose of slow release is achieved and the action time of the tilmicosin is prolonged.

The invention discloses a leucoderma covering agent. The leucoderma covering agent is a covering liquid or covering cream, wherein the covering liquid mainly comprises 1,2-propyleneglycol, jojoba oil, a preservative, a surfactant, vitamin E acetate, 1,3-dihydroxyacetone, an edible pigment and deionized water; and the covering cream mainly comprises magnesium aluminum silicate, 1,2-propyleneglycol, methyl parahydroxybenzoats, propyl p-hydroxybenzoate, imidazolidinyl urea, talcpowder, titanium dioxide, iron oxide, jojoba oil, vegetable fat, vitamin E acetate, stearyl alcohol, stearic acid, decapolyglycerol monooleate, diolein, triethanolamine and deionized water. The covering liquid has waterproof, sweatproof and wear-resistant effects, and is durable; the covering cream is quick in coloration and natural in color formation, and is convenient to use; and the covering liquid and the covering cream are combined to provide comprehensive covering for leucoderma patients.

The invention discloses anti-dandruff shampoo with an effect of improving the microbial flora on the scalp skin. The anti-dandruff shampoo is prepared from the following raw materials: water, polydimethylsiloxane, glycol stearate, sodium lauroyl sarcosine, polyquaternium-10, cetostearyl alcohol, ammonium chloride, vaccinium uliginosum berry extract, celery seed extract, silk hydrolysate, zinc pyrithione, piroctone olamine, EDTA disodium, surfactant, preservatie, artemisinin and rosemary water. The invention further discloses a preparation process of the shampoo. The shampoo can be used for improving the microbial environment of the scalp skin and improving the resistance of the scalp skin and can achieve the effect of effectively removing dandruff and preventing dandruff reoccurrence.

The invention discloses an eye shadow and a preparation method thereof. The eye shadow comprises the following components in percentage by weight: 15-28% of a lubricant, 1-5% of an anti-caking agent, 10-18% of a filling agent, 0.1-5% of a coloring agent, 0.7-1.34% of a preservative, 0.1-5% of tin oxide, 0.1-5% of calcium aluminum borosilicate, 6.1-10.2% of a moisturizing agent, 18-25% of emollient, 2-4% of surface active agent, 1-2% of stearyl alcohol, 0.1-0.5% of pentaerythritol tetraester, 1-3% of an elderberry extract, 1-3% of a camellia japonica extract, 1-3% of a lilium candidum flower extract and the balance of water. The eye shade and the preparation method disclosed by the invention have the advantages that the makeup process is smooth, the mildness without stimulation is achieved, the moisturizing and water-supplementing effects are achieved and the skin is repaired, and after use, the skin is moisturized and bright, soft and elastic, so that thin veins and brown stains can be effectively reduced.

The invention aims at providing an anti-drag aqueous fracturing fluid preparation, and provides a single-dosage anti-drag aqueous fracturing fluid preparation in order to overcome defects during preparation of anti-drag aqueous fracturing fluid and construction. The preparation can be compounded with water in any proportions, is good in solubility, meets the requirement on continuous mixing during on-site construction of shale gas, and has an important application value in shale gas exploration. The anti-drag aqueous fracturing fluid preparation comprises the following components by weight percentage: 4-6% of anti-drag agent, 8-12% of clay stabilizing agent, 1-3% of cleanup additive, and the balance of water, wherein the anti-drag agent is a bipolymer of acrylamide and polyethylene glycol oxide ether acrylate; the clay stabilizing agent is polydimethyl propylenediene ammonium chloride; and the cleanup additive comprises the following components by mass percentage: 9-11% of perfluorooctanoyl ethylene amino methyl diethyl ammonium iodide, 20-30% of polyoxyethylene 2,5-dimethyl stearyl alcohol ether, and 20-30% of isopropanol.

Compositions and methods are disclosed for producing pearlized compositions of alcoholic hydrogels at ambient temperatures. More particularly, compositions and methods are disclosed for pearlized alcoholic hydrogel compositions with stearyl alcohol at preparation temperatures below the melting point of stearyl alcohol, which is solid at room temperature. Pearlizing effects are achieved in alcoholic hydrogels at low temperatures by the addition to the alcoholic hydrogel of stearyl alcohol in a siloxane form as stearyl alcohol trialkylsiloxane. By incorporating the siloxane form of stearyl alcohol, which previously could be only handled at anhydrous conditions, into the hydroalcoholic gel, one obtained a stable pearlized alcoholic hydrogel having a lustrous pearlescent appearance. Preparation was accomplished without heating above room temperature, without a pearlescent wax, and without a potentially skin irritating surfactant.

The invention discloses a nursing agent for skin moisturizing and repairing. The nursing agent for skin moisturizing and repairing comprises the following components by mass percentage: 0.05 0.15% ofdisodium EDTA, 0.5-3.0% of nicotinamide, 2.0-5.5% of glycerin, 2.5-5.5% of propylene glycol, 0.05-0.35% of xanthan gum, 0.05-0.5% of sodium hyaluronate, 0.15-0.5% of p-hydroxyl acetophenone, 1.0-5.0%of caprylic/capric triglyceride, 1.0-3.0% of polydimethylsiloxane, 1.0-5.0% of isononyl isononanoate, 0.5-5.0% of jojoba seed oil, 0.5-2.5% of avocado tree fruit oil, 1.75-10.5% of repair essential oil, 0.05-0.5% of fullerenes, 0.35-2% of repairing essence, 0.2-3.5% of cetostearyl alcohol, 1.0-2.5% of cetearyl olivate, 1.0-2.5% of sorbitan olivate, 0.1-1.0% of lecithin, 0.5-5.0% of oligopeptide-1, 0.1-0.5% of D-panthenol, 0.5-2.5% of a Centella asiatica extract, 0.5-2.5% of 1,2-hexanediol, and the balance of deionized water. The product of the invention can quickly improve the moisture retention of the skin, obviously improves the dryness of the skin, increases the moisture content in the skin, and makes the skin appear young. .

The invention discloses an enrofloxacin microcapsule preparation and a preparation method thereof. The enrofloxacin microcapsule preparation is prepared by 5 percent to 90 percent of enrofloxacin raw material and 95 to 10 percent of accessories, and the accessory is one of the followings or a mixture mixed by a plurality of the followings: 12 to 18 carbon fatty acid, calcium stearate monoglycerol ester, stearyl alcohol, saturated triglyceride, glycerol monoester, paraffin, animal wax, vegetable wax and fat powder, etc.. The appearance of the enrofloxacin microcapsule preparation is a white or light yellow spherical granule, the dispersion performance is good, the used accessory is safe, and the enrofloxacin microcapsule preparation has no toxicity or side effects for livestock and poultry and has a gradual release in stomach and intestine, thus maintaining the durability of the efficacy.

The invention provides a bath cream and a preparation method thereof. The bath cream mainly comprises the following components in weight percent: 12-20% of surface active agent, 3-7% of crylic acid (ester)/stearyl alcohol polyether-20 methacrylate copolymer, 0.5-1% of coconut oil amide DEA, 0.05-0.3% of methyl isothiazolinone, 0.3-0.5% of sodium hydroxide, 0.5-1% of dehydrated plant smashed particles and 1-1.5% of sodium chloride. The bath cream of the invention improves the utilization efficiency of plants, and plays a certain action of massage on skins by adding stable suspended dehydrated plant smashed particles, and improves the cleaning efficacy of the bath cream.

The invention discloses an organic reversible thermochromic microcapsule with long service life and large color difference and a preparation method thereof. A wall material of the organic reversible thermochromic microcapsule is prepared from the following raw materials in percentage by weight through polymerization: 30-95% of acrylate and/or methacrylate, 5-70% of a divinyl and/or polyvinyl monomer mixture, and 0-10% of an acrylic acid and/or methacrylic acid mixture, and a core material is composed of a colour former 3,3-di(4-dimethylaminophenyl)-6-dimethylamino phthalide, a color developing agent 4,4'-dihydroxydiphenylsulfone, and a solvent selected from 1-dodecanol, 1-tetradecanol, 1-hexadecanol and 1-octadecanol; and the preparation method is implemented through carrying out prepolymerization on monomers and carrying out suspension polymerization on the obtained product. The obtained organic reversible thermochromic microcapsule has the advantages of long service life and large color difference; the microcapsule does not release formaldehyde, and does not contain bisphenol A, so that the microcapsule is safer to use.

The invention discloses an amino acid anti-aging cream which comprises three components A, B and C in parts by weight, the component A comprises the following materials in parts by weight: 18-25 parts of ozocerite, 4-7 parts of octadecanoic acid, 4-6 parts of stearyl alcohol, 2-5 parts of sp-60, 2-4 parts of Tween-60, 1-3 parts of hydrogenated lanolin, 1-2 parts of beewax and 0.1-0.3 part of propyl p-hydroxybenzoate; the component B comprises the following materials of 50-60 parts of distilled water, 3-8 parts of propylene glycol, 3-5 parts of cysteine, 1-3 parts of gamma-amino-beta-hydracrylic acid and 0.1-0.3 part of methyl parahydroxybenzoats; and the component C comprises the following material of 0.5-1 part of essence.