- Novel process for preparing sun-screening agent 2-hydroxy-4-n-octyloxy benzophenone
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The invention discloses a novel process for preparing a sun-screening agent 2-hydroxy-4-n-octyloxy benzophenone. According to the process, 2,4-dihydroxy benzophenone is prepared, and 2,4-dihydroxy benzophenone and 1-chloro-n-octane are used as raw materials, wherein the prepared 2,4-dihydroxy benzophenone is simple in method, has no need of posttreatment and can be directly used as a reaction rawmaterial for subsequent reaction, and the energy consumption is reduced from the source; 1-chloro-n-octane is taken as an alkylation reagent, inorganic base is taken as a catalyst, solvents are addedfor reaction, and the yield of the obtained product 2-hydroxy-4-octyloxybenzophenone is high and can reach 90% or above. According to the method, the raw material cost is reduced, the problem of industrial wastewater at present is solved, in addition, the whole process is mild in condition, few in three wastes, high in yield and good in product quality, the use requirements of the cosmetic industry are met, the technological process is simple to operate and easy to realize, the intermediate reaction process is simple and easy to control, and industrial production can be realized.
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Paragraph 0097-0104
(2021/02/06)
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- Process for synthesizing UV-531 by chloro-n-octane
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The invention discloses a process for synthesizing UV-531 (2-hydroxy-4-n-octyloxy benzophenone) by chloro-n-octane. According to the process, chloro-n-octane and UV-0 (2,4-dihydroxy benzophenone) areused as raw materials, potassium carbonate and sodium carbonate are used as catalysts, and 2-hydroxy-4-n-octyloxy benzophenone is synthesized. According to the process, 2-hydroxy 4-n-octyloxy benzophenone and chloro-n-octane are used as raw materials, cheap alkali is used as a catalyst, non-toxic PEG is used as a phase transfer catalyst, the reaction conditions are mild, the production operation is simple and convenient, the safety is high, the complete yield of the reaction is high, the cost is low, and the process is suitable for industrial production.
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Paragraph 0018-0023
(2021/01/15)
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- Cosmetic compositions
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Suggested is a cosmetic compositions comprising (a) a crosspolymer obtained from copolymerisation of at least two different polyols and at least one dicarboxylic acid and (b) at least one fragrance.
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- A composition for lightening skin and hair
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Suggested is a composition comprising (a) sclareolide and (b1) at least one tyrosinase inhibitor; and/or (b2) at least one sun protection factor; and/or (b3) at least one anti-oxidants; and/or (b4) at least one anti-inflammatory agent; and/or (b5) at least one desquamating agent.
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- Substituted hexahydro-1,4-diazepin-5-ones and compositions stabilized therewith
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The instant invention pertains to white, dyed, dipped, unscented and/or scented candle wax which is effectively stabilized against discoloration and fading by the incorporation therein of a substituted hexahydro-1,4-diazepin-5-ones in combination with a UV absorber and/or an antioxidant. Additionally, some novel substituted hexahydro-1,4-diazepin-5-one compounds are described.
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- SUNSCREEN COMPOSITIONS
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The present invention relates to improved sunscreen compositions, more preferably to improved sunscreen compositions containing at least one sunscreening agent (sunscreen) and a silicone-polyamide copolymer.
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- Method of purifying arylphenones
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Hydroxy and alkyloxy benzophenones, also known as arylphenones, are efficiently and economically purified by contacting them with inorganic phosphorous compounds in the presence of a non-polar solvent. Best results are obtained when the arylphenone is then treated with an activated carbon and/or activated clay.
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- Phosphites and their production and use
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Phosphites represented by the general formula (I): STR1 wherein R1, R2, R4 and R5 independently represent a hydrogen atom, an alkyl group having 1 to 8 carbon atoms, a cycloalkyl group having 5 to 8 carbon atoms, an alkylcycloalkyl group having 6 to 12 carbon atoms, an aralkyl group having 7 to 12 carbon atoms or a phenyl group; R3 and R6 independently represent a hydrogen atom or an alkyl group having 1 to 8 carbon atoms; X1 is a dihydric alcohol residue, wherein HO--X1 --OH defines the corresponding dihydric alcohol from which residue X1, is obtained; and X2 is a direct bond or an alkylene group having 1 to 8 carbon atoms; and the phosphites are useful as stabilizers for organic materials.
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- Piperidine compound, a process for producing the same and a stabilizer using the same
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2-Methyl-3-(2,2,6,6-tetramethyl-4-piperidylamino)-N-(2,2,6,6-tetramethyl-4-piperidyl)-propionamide represented by the following formula, a process for producing the same and a stabilized organic material composition containing the same wherein the piperidine compound imparts excellent properties, such as light stability or thermal stability to the organic materials. STR1
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- Light-stable screening cosmetic composition containing bixin combined with a lipid-soluble UV filter and its use for protecting the human epidermis against ultra-violet radiation
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The invention relates to a light-stable cosmetic composition for protecting the human epidermis against UV radiation, containing at least 0.0025% by weight of bixin combined with at least 1% by weight of one or more lipid-soluble agents screening UV radiation, chosen from 3-benzylidene-dl-camphor, its derivatives and benzophenone derivatives, in a cosmetically acceptable vehicle comprising at least one fatty phase. The bixin takes the form of an oily extract of annatto containing at least 0.1% by weight of bixin.
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- Method of treating inflammation
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A method of treating inflammation and inhibiting prostaglandin synthesis employing 2-hydroxybenzophenone and substituted 2-hydroxybenzophenones.
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- High molecular weight piperidine derivatives as UV stabilizers
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Substituted high molecular weight hindered spiropiperidine compounds and polymer compositions stabilized by these compounds. The spiropiperidine compounds are prepared by reacting hindered 4-piperidinone hydrochloride with an activated benzene, such as resorcinol, in an acid medium.
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- 1-Aza-4-thiacyclohexane-4,4-dioxide derivatives
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New 1-aza-4-thiacyclohexane-4,4-dioxide derivatives are used alone or in combination with other stabilizers for stabilizing organic materials. The new compounds are prepared by reacting substituted diallylsulfides with ammonia, amines or hydrazines.
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