Abstract: The invention relates to a solid redispersible emulsion, which is comprised of an oil-in-water emulsion consisting of a laundry care constituent, which is encapsulated in an enclosure. This enclosure is stabilized by polyvalent metal ions and, initially, is water-insoluble and is rendered soluble by adding metal ions. The enclosure material is preferably a biodegradable material and, in particular, a polysaccharide, such as alginates, pectins or carageenans. These solid and redispersible emulsions are used, in particular, in laundry care products.

Abstract: The invention relates to a solid redispersible emulsion, which is comprised of an oil-in-water emulsion consisting of a laundry care constituent, which is encapsulated in an enclosure. This enclosure is stabilized by polyvalent metal ions and, initially, is water-insoluble and is rendered soluble by adding metal ions. The enclosure material is preferably a biodegradable material and, in particular, a polysaccharide, such as alginates, pectins or carageenans. These solid and redispersible emulsions are used, in particular, in laundry care products.

Abstract: The invention relates to a method for chemically modifying polysaccharides with the aid of a mechanical device and of at least one modifying reagent. The method is characterized in that the polysaccharide constituent is subjected at least once to a treatment by a roll mill during which at least two adjacent and counter-rotating rolls rotate at different speeds, and the polysaccharide constituent is mixed with the modifying reagent before and/or during the mechanical treatment. During this method, typically pectins, carob seed grain, guar meal and alginates are used as the polysaccharide constituent, and epoxides, amines or carboxylic acid derivatives are used as modifying reagents. The mechanical treatment can be repeated one to three times in a multiple roll mill, preferred rotating speeds of the adjacent rolls typically differing by 200%.

Abstract: PEG-free, cold-preparable, prolonged-stability, low-viscosity, fine oil-in-water emulsions, their preparation from preferably clear oil phases or via preferably clear to transparent microemulsion-like concentrates, the corresponding oil phases or microemulsion-like concentrates and the use of the inventive emulsions for producing cosmetic, dermatological, pharmaceutical or industrial formulations, especially for the production of impregnating emulsions for wet wipes or for sprayable care emulsions are provided.

Abstract: The invention relates to polysaccharide derivatives consisting of a biopolysaccharide skeleton and organic groups with a molecular weight <5 000 that are connected to said skeleton via ether bridges. The organic groups have the general formula (Ia) or (Ib). Preferably, ?- or ?-(1,4)- and/or ? or ?-(1,3)-glucan units are used as the biopolysaccharide component, such as e.g. xy-loglucans, glucomannans such as guar gum or locust bean gum, xanthan gum, carrageenans, alginates and pectins. The invention also relates to a method for producing said polysaccharide derivatives, according to which the biopolysaccharide component is reacted with an N-alkyl maleamic acid or a salt thereof in the presence of a base catalyst, whereby the maleamide component can also be cyclised prior to or following the reaction with the biopolysaccharide component.

Abstract: Disclosed is a method for producing flavor-active terpenes from terpene hydrocarbons. According to said method, a lyophilized mycel which is first rehydrated and is then mixed with the substrate is used preferably in a submerged culture in the framework of selective biotransformation with the aid of microorganisms. The inventive method, which can be carried out especially in an enantioselective, stereoselective, and/or regioselective manner, makes it possible to obtain terpenoid alcohols, epoxides, alde-hydes, ketones, polyalcohols, carbonyls, and carbonyl alcohols with the aid of fusarium, pleutorus, penicillium, and chaetomium species, the obtained substances being isolated particularly from cellular components. Said method should be carried out above all in a stirred tank, surface reactor, or fixed bed reactor while preferably taking place in a two-phase system with reduced carbon source moieties.

Abstract: The claimed method for preparing conjugated polyunsaturated fatty acid esters consisting of an alcohol radical R1 having from 1 to 5 carbon atoms and a fatty acid radical R2 having from 10 to 24 carbon atoms, together with alkoxides having from 1 to 5 carbon atoms, comprises carrying out the reaction solvent-free using a phase-transfer catalyst. In this method, the contents of the fatty acid ester should be from 85 to 99.9% by weight, those of the alkoxide component from 0.05 to 10% by weight, and those of the phase-transfer catalyst from 0.05 to 5.0% by weight, in each case based on the total reaction mixture. Esters of linoleic acid and linolenic acid are preferred as starting material, just as sodium or potassium methoxide or sodium or potassium ethoxide are preferred as alkoxide. Suitable phase-transfer catalysts are, for example, polyethylene glycols, polyethylene glycol monomethyl ethers or polyethylene glycol dimethyl ethers, crown ethers and quaternary ammonium or phosphonium salts.