Abstract: The present invention relates to a specific hydrocarbon mixture comprising at least 95% by weight of saturated linear C-13 hydrocarbon based on the sum of the hydrocarbons in the hydrocarbon mixture, characterized in that the amount of C11/C12 is 0.05 to 1.5% by weight based on the sum of the hydrocarbons in the hydrocarbon mixture and the amount of C14 to C17 is 0.2 to 3.5 % by weight based on the sum of the hydrocarbons in the hydrocarbon mixture and the use thereof in cosmetic and/or pharmaceutical formulations, and to cosmetic formulations comprising the hydrocarbon mixture.

Abstract: Continuous reductive dehydroxymethylation process for the preparation of alkanes from primary aliphatic alcohols, having 3 to 25 carbon atoms, in the presence of hydrogen and a catalyst in a reactor at a pressure of ?2 bar, characterized in that the dehydroxymethylation takes place in the vapor phase.

Abstract: The invention relates to biobased waxy esters which in particular in the form of wax dispersions bring about cloudiness and/or pearlescence in cosmetic cleansers. The invention further provides the use of the waxes in cosmetic compositions, the production thereof and the cosmetic compositions themselves.

Abstract: The disclosure relates to dialkyl carbonates of branched alcohols and their use in cosmetic and/or pharmaceutical compositions. The disclosure more particularly relates to dialkyl carbonates in which the alkyl groups are both 2-propyl-1-heptyl groups.

Abstract: The invention relates to a hydrocarbon mixture that contains at least two hydrocarbons that are different from each other, the number of carbons thereof differing by more than one, wherein said two hydrocarbons that differ from each other make up at least 60% by weight, preferably at least 70% by weight of the total of the hydrocarbons. The invention also relates to the use of said hydrocarbon mixtures and to cosmetic and/or pharmaceutical preparations containing said hydrocarbon mixtures.

Abstract: Disclosed is the use of the compounds (A) corresponding to formula wherein R1 represents C6-C24alkyl; R2 is hydrogen; or C1-C4alkyl; R3 is a radical of formula (1a) *—(CH2)n1—R4 R4 is a heterocyclic or aromatic radical comprising 4 to 6 carbon atoms which can contain from 1 to 3 nitrogen and/or oxygen atoms; n1 is a number from 0 to 5; or R2 and R3 together with the linking nitrogen atom form a heterocyclic radical comprising 4 to 6 carbon atoms which can contain one or more oxygen or nitrogen atoms; as solubilizing agent for organic UV filters (B) selected from (B1) benzophenone derivatives, (B2) hydroxyphenyl triazine derivatives; and (B3) trianilino-s-triazine derivatives.

Abstract: The present invention relates to a process for the manufacture of hydroxy-substituted aromatic styryl or stilbene compounds.

Abstract: The present invention relates to a composition comprising isosorbide monooleate, a first surfactant selected from the group consisting of an alkyl glycoside having a weight average of the number of C-atoms in the alkyl chain of more than 11, cocoamidopropyl betaine and mixtures thereof, a second surfactant which is an alkyl glycoside having a weight average of the number of C-atoms in the alkyl chain of less than 11 and water. Furthermore it relates to a process for making this composition and to a cosmetic formulation, comprising this composition.

Abstract: The present invention relates to a method for preparing a compound of the formula (I) with a specific definition of the substituent R3 a mixture and also a corresponding application/use.

Abstract: A cosmetic or pharmaceutical composition is provided. The composition contains a mixture of oils prepared by Kolbe electrolysis of branched chain fatty acids and mixtures of branched chain fatty acids with straight chain fatty acids. The fatty acids containing from 3 to 26 carbon atoms. The oils are a mixture of oils with different spreading rates (spreading cascade).

Abstract: A process is provided for the production of linear saturated alkanes from one or more primary alcohols, wherein the carbon chain of the one or more primary alcohols has one carbon atom more than the alkane, including conducting reductive dehydroxymethylation of one or more primary fatty alcohols containing 8 to 24 carbon atoms, at a temperature ranging from 100 to 300° C. and pressures from 1 to 250 bar in the presence of hydrogen and a catalyst, and removing water formed during the reaction.

Abstract: The present invention relates to a method for preparing a compound of the formula (I) with a specific definition of the substituent R3 a mixture and also a corresponding application/use.

Abstract: The present invention relates to novel mono- and diesters of 2,5-di(hydroxymethyl)tetrahydrofuran, processes for their preparation by esterification in the presence of tertiary amines or in the presence of enzymatic esterification catalysts and the use of these mono- and diesters as interface-active compounds, rheology modifiers and emollients. The invention further relates to cosmetic and pharmaceutical compositions, and to detergents, cleaners and dishwashing compositions which comprise these mono- and diesters of 2,5-di(hydroxymethyl)-tetrahydrofuran.

Abstract: The disclosure relates to dialkyl carbonates of branched alcohols and their use in cosmetic and/or pharmaceutical compositions. The disclosure more particularly relates to dialkyl carbonates in which the alkyl groups are both 2-propyl-1-heptyl groups.

Abstract: The present invention relates to the use of a cosmetic composition comprising isosorbide monooleate for depositing isosorbide monooleate on human skin or hair. Furthermore it relates to a process for depositing isosorbide monooleate on human skin or hair, wherein this process comprises contacting human skin or hair with a cosmetic composition comprising isosorbide monooleate and rinsing off the cosmetic composition comprising isosorbide monooleate with water, so that, after rinsing off the cosmetic composition, isosorbide monooleate is left deposited on the human skin or hair.

Abstract: The present invention relates to a composition comprising isosorbide monooleate, a first surfactant selected from the group consisting of an alkyl glycoside having a weight average of the number of C-atoms in the alkyl chain of more than 11, cocoamidopropyl betaine and mixtures thereof, a second surfactant which is an alkyl glycoside having a weight average of the number of C-atoms in the alkyl chain of less than 11 and water. Furthermore it relates to a process for making this composition and to a cosmetic formulation, comprising this composition.

Abstract: The invention relates to a hydrocarbon mixture that contains at least two hydrocarbons that are different from each other, the number of carbons thereof differing by more than one, wherein said two hydrocarbons that differ from each other make up at least 60% by weight, preferably at least 70% by weight of the total of the hydrocarbons. The invention also relates to the use of said hydrocarbon mixtures and to cosmetic and/or pharmaceutical preparations containing said hydrocarbon mixtures.

Abstract: Disclosed is the use of the compounds (A) corresponding to formula wherein R1 represents C6-C24alkyl; R2 is hydrogen; or C1-C4alkyl; R3 is a radical of formula (1a) *—(CH2)n1—R4 R4 is a heterocyclic or aromatic radical comprising 4 to 6 carbon atoms which can contain from 1 to 3 nitrogen and/or oxygen atoms; n1 is a number from 0 to 5; or R2 and R3 together with the linking nitrogen atom form a heterocyclic radical comprising 4 to 6 carbon atoms which can contain one or more oxygen or nitrogen atoms; as solubilizing agent for organic UV filters (B) selected from (B1) benzophenone derivatives, (B2) hydroxyphenyl triazine derivatives; and (B3) trianilino-s-triazine derivatives.

Abstract: The invention relates to esters of 2-propylheptanoic acid and also to the use of esters of 2-propylheptanoic acid in cosmetic and/or pharmaceutical preparations. The compounds are characterized by the particularly lightweight sensation thereof.

Abstract: Mixtures of Guerbet alcohols, their use in cosmetic and/or pharmaceutical preparations, and also cosmetic and/or pharmaceutical preparations comprising mixtures of Guerbet alcohols are described. Of suitability as petroleum jelly substitute are in particular Guerbet alcohol mixtures with a melting range, measured by differential scanning calorimetry (DSC), between ?20° C. and +70° C., where the width of the melting range comprises at least 30 temperature degrees and the maximum of the melting range is 35±10° C. These are obtainable for example by reacting a) 55 to 95% by weight of cetylstearyl alcohol, b) 5 to 45% by weight of fatty alcohols with a chain length of from 8 to 22 carbon atoms and c) optionally an aliphatic diol having at least 3 carbon atoms.