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| Number | Title | Issue Date |
| 4246285 | Skin conditioning compositions containing guanidine inorganic salts A skin conditioning composition containing a guanidine inorganic salt. The compositions are in the form of lotions, creams, solutions, gels, and solids.... | 01/20/1981 |
| 4226889 | Cosmetic stick composition Solid, stick-type cosmetic compositions consist essentially of from about 1 to about 30 parts by weight of sodium stearate, 100 parts by weight of water and an "active" material intended to be applied to the skin. The composition also preferably contains ... | 10/07/1980 |
| 4224311 | Disubstituted derivatives of glycerol and cosmetic compositions containing the same as an oily excipient therefor A disubstituted derivative of glycerol has the formula ##STR1## wherein one of Z1 and Z2 represents -YR' and the other represents hydroxy, R and R' represent a saturated and branched hydrocarbon residue of a ROH or R'OH alcohol ... | 09/23/1980 |
| 4219450 | Propene trimer and tetramer oximes in perfumes Oximes of propene trimers and propene tetramers are disclosed which are new compositions of matter. These oximes are useful as perfume components in, e.g., colognes and perfumes and as fragrances in detergents and cosmetics.... | 08/26/1980 |
| 4217253 | Mixture of 3-methyl-1-phenyl-pentanol-5 or its isomers and butanoyl cyclohexane derivatives Processes and compositions are described for the use in perfume aroma augmenting, modifying, altering and enhancing compositions and as perfume, cologne and perfumed article aroma imparting materials of mixtures of 3-methyl-1-phenyl-pentanol-5 and one or ... | 08/12/1980 |
| 4211674 | Cyclic acetals and ketals and their use in perfume compositions Novel tricyclic 1,3-dioxanes based on the skeleton of 1,1-dimethyloctalin or 1,1-dimethyldecalin and their use as perfume components is disclosed.... | 07/08/1980 |
| 4209503 | Food composition containing whey colloidal precipitate A food-grade composition comprises a food of food-grade material, whey colloidal precipitate and water. The whey colloidal precipitate may effect the physical properties of clouding, stabilizing, gelling and emulsifying. The whey colloidal precipitate is ... | 06/24/1980 |
| 4206090 | 3-Methyl-1-phenyl-pentanol-5 or its isomer and butanoyl cyclohexane derivatives Processes and compositions are described for the use in perfume aroma augmenting, modifying, altering and enhancing compositions and as perfume, cologne and perfumed article aroma imparting materials of mixtures of 3-methyl-1-phenyl-pentanol-5 and one or ... | 06/03/1980 |
| 4201697 | Perfumery uses of oxyhydrocarbylnorbornane derivatives Processes and compositions are described for the use in perfume aroma augmenting, enhancing, modifying and imparting compositions and as perfume and perfumed article aroma imparting and enhancing materials of oxyhydrocarbylnorbornanes having the structure... | 05/06/1980 |
| 4193989 | Sunscreen gel A water-resistant suntan gel comprising an alcoholic solvent, a sunscreen agent, emollients, a selected acid which enhances the binding ability of the gel film to the skin and a gelling agent for the solvent. The composition prevents sun damage to the ski... | 03/18/1980 |
| 4190561 | Esters of cyclohexene, odoriferous compositions containing said esters and process for the preparation thereof Novel esters of cyclohexene are disclosed having the formula ##STR1## in which R represents hydrogen or a hydrocarbon group containing from 1 to 6 carbon atoms. These novel esters display a wide range of interesting odoriferous properties. A process ... | 02/26/1980 |
| 4181631 | Alpha-hydroxyalkyl-4-tertiary-alkylcyclohexane perfume compositions Novel -hydroxyalkyl-4-t-alkylcyclohexanes possessing a sandalwood note, their utility as olfactory agents, and perfume compositions containing them.... | 01/01/1980 |
| 4177170 | 3,3,7,8-Tetramethyl-2-oxabicyclo-[4,4,0]-decane derivatives and their use in perfume compositions Compounds having the formula: ##STR1## wherein X represents a hydrogen atom or an alkyl group m has a value of 0 or 1, n has a value of 1 or 2 and n+m=2 are novel. They possess unique floral odors and are useful as ingredients of compounded perfumery... | 12/04/1979 |
| 4170577 | 2,3-Dimethyl-5-(2,2,3-trimethyl-3-cyclopenten-1-yl)-2-pentanol perfume compositions 2,3-Dimethyl-5-(2,2,3-trimethyl-3-cyclopenten-1-yl)-2-pentanol possesses a strong body woody, oily, sandalwood note reminiscent of sandalwood oil and is especially valuable in fragrance compositions, perfumed articles and colognes.... | 10/09/1979 |
| 4144199 | Safranic acid ester perfume compositions Safranic acid esters having the general formula ##STR1## wherein the dotted lines represent two conjugated double bonds in the positions 2 endocyclic and 4 (-isomer), 1 and 3 (ଲ-isomer) or 2 exocyclic and 3 (γ-isomer), R1 rep... | 03/13/1979 |
| 4142998 | Uses of alpha methyl styrene dimers in perfumery processes and products A process is described for providing clear extended compositions of essential oils which comprises a composition of an essential oil and an extender material miscible with said essential oil which does not appreciably alter the aroma of the essential oil ... | 03/06/1979 |
| 4137305 | Cyclic amides having a physiological cooling effect Cyclic and acyclic amides, substituted ureas and sulphonamides are disclosed having the property of stimulating the cold receptors of the nervous system of the body to produce a cold sensation and are used for this purpose in a variety of edible and topic... | 01/30/1979 |
| 4137302 | Cosmetic composition A cosmetic composition for the treatment of human skin comprises monoacetyl urea dispersed or dissolved in a vehicle other than water. The composition may form a liquid or a solid.... | 01/30/1979 |
| 4137304 | Cyclic substituted ureas having a physiological cooling effect Cyclic and acyclic amides, substituted ureas and sulphonamides are disclosed having the property of stimulating the cold receptors of the nervous system of the body to produce a cold sensation and are used for this purpose in a variety of edible and topic... | 01/30/1979 |
| 4136164 | Certain substituted amides having a physiological cooling effect Cyclic and acyclic amides, substituted ureas and sulphonamides are disclosed having the property of stimulating the cold receptors of the nervous system of the body to produce a cold sensation and are used for this purpose in a variety of edible and topic... | 01/23/1979 |
| 4132677 | Perfume compositions containing 2-(2-cyanoethylidene)-2-methyl-bicyclo(2.2.1)hept-5-enes Novel 2-(2-cyanoethylidene)-bicyclo[2.2.1]hept-5-enes and hydrogenated derivatives thereof, their utility as olfactory agents, and perfume compositions containing them.... | 01/02/1979 |
| 4132676 | Perfume compositions containing ethyl 3,4-dichloro-5-isothiazolecarboxylate Ethyl 3,4-dichloro-5-isothiazolecarboxylate possesses a minty anise odor which is valuable in perfumery.... | 01/02/1979 |
| 4132675 | CIS-Oct-6-en-1-al perfumes CIS-Oct-6-en-1-al is a novel unsaturated aldehyde which possesses useful perfuming and flavoring properties. Use of said aldehyde as perfume and flavor ingredient.... | 01/02/1979 |
| 4130509 | Perfume compositions containing cis- and trans-trimethylcyclohexylethyl ethers A perfumery composition consisting essentially of from 1% to 50% by weight of cis- and trans-trimethylcyclohexylethyl ethers of the formulae: ##STR1## and the remainder customary constituents of perfumery compositions; and a process for producing tra... | 12/19/1978 |
| 4130508 | Perfume compositions containing cyclohexadiene derivatives Processes and compositions are described for use in foodstuff, chewing gum, toothpaste and medicinal product flavor and aroma; tobacco flavor and aroma; perfume and perfumed article aroma augmenting, enhancing and imparting compositions; and as foodstuff,... | 12/19/1978 |
| 4126702 | Novel derivatives of glycerol Novel bi-substituted derivatives of glycerol of the formula: ##STR1## wherein X and Y, which can be the same or different, are either --O-- or ##STR2## where R1 is a branched alkyl radical having from 5 to 8 carbon atoms, with the num... | 11/21/1978 |
| 4126585 | 2-Methyl-2-ethyl-hexanoate ester perfume compositions 2-Methyl-2-alkyl-alkanoic acid esters of the formula ##STR1## wherein R1 is a saturated or unsaturated, straight- or branched-chain aliphatic hydrocarbon radical having 1 to 5 carbon atoms, and R2 and R3 are independe... | 11/21/1978 |
| 4125549 | Process for the manufacture of cosmetic quality isooctyl neodecanoate Cosmetic quality isooctyl neodecanoate is manufactured by contacting an alcohol mixture containing a major amount of isooctyl alcohol with neodecanoic acid in the presence of an acid catalyst and at a temperature of from about 160° C. to about 230° C. t... | 11/14/1978 |
| 4123393 | Substituted-norbornane perfume compositions Substituted norbornane derivatives are described for use as perfumes, colognes, and in perfumes aroma augmenting, modifying, enhancing and imparting compositions. The substituted norbornane derivatives have the following structure: ##STR1## wher... | 10/31/1978 |
| 4122023 | Synthetic saturated oils, and their production and use Synthetic saturated oils useful as materials for lubricating oils and cosmetics and prepared by hydrogenation of low molecular weight polyisoprene having the 1,4 structure of at least 70% in the main chains and a number average molecular weight of about 2... | 10/24/1978 |
| 4119577 | Substituted-norbornane perfumes compositions Substituted-norbornane derivatives are described for use as perfumes, colognes and in perfume aroma augmenting, modifying, enhancing, and imparting compositions. The substituted norbornane derivatives having the following structure: ##STR1## whe... | 10/10/1978 |
| 4119574 | 4-Hydroxy-2,4,6,6-tetramethyl cyclohex-2-en-1-one perfume compositions Processes and compositions are described for the use in perfume and perfumed article aroma augmenting, enhancing and imparting compositions and as perfume and perfumed article aroma imparting materials of hydroxy cyclohexenone derivatives having the gener... | 10/10/1978 |
| 4115313 | Bile acid emulsions The invention is directed to emulsion compositions of, or including, bile acids, their conjugates, lower alcohol esters or salts of said acids or conjugates; water to effect solution of one or more of said defined bile acids; and at least one of: glycerid... | 09/19/1978 |
| 4098882 | Anti-solar composition Anti-solar cosmetic composition containing as the protective agent against actinic rays a compound of the formula ##STR1## wherein R3 is hydrogen, --COR1 or --CHOHR1 wherein R1 is CH3 and R4... | 07/04/1978 |
| 4078147 | Hydroxy acid esters of higher alcohols Hydroxy diester compounds are obtained by esterification between malic acid or tartaric acid and a saturated, aliphatic alcohol of 16 or more carbon atoms having side chains. These compounds are a colorless, odorless synthetic oil with low cloud point, wh... | 03/07/1978 |
| 4066789 | Blends of lanolin wax and esters of aliphatic polyols and fatty acids Blends of the hard wax fraction obtained from the fractionation of lanolin and an ester derived from an aliphatic polyol or ether polyol and fatty acid are suitable substitutes for U.S.P. anhydrous lanolin and can be substituted therefore in cosmetic form... | 01/03/1978 |
| 4061780 | Cosmetic oil containing isobutylene Polymers of C4 olefins having a viscosity of 15 to 35 centistokes at 100° F show improved performance as cosmetic oils, in comparison with squalane. These polymers are prepared by polymerizing (a) isobutylene by itself, or (b) C4 hydrocarbon olefin conta... | 12/06/1977 |
| 4032588 | Process for preparing 2,6,10,15,19,23-hexamethyltetracosane A non-irritating base component useful for cosmetics and topical preparations consisting of 2,6,10,15,19,23-hexamethyltetracosane having a high stability and being very safe for use on skin are hereby disclosed. Said component is synthesized by (a) prepar... | 06/28/1977 |
| 4014995 | Cosmetics containing finely divided oat flour Improved cosmetic preparations are obtained by inclusion of a particular oat flour.... | 03/29/1977 |
| 4001141 | Cosmetic emulsifiers An emulsifying and peptizing agent having the formula wherein R is a lipophilic hydrocarbon residue of a member selected from the group consisting of alcohols, sterols and their mixtures derived from a member selected from the group consisting of (a) hydrogena... | 01/04/1977 |
