Composition combination containing enriched hill shaddock oil
US-2024325485-A1 · Oct 3, 2024 · US
US11540987B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-11540987-B2 |
| Application number | US-201515781321-A |
| Country | US |
| Kind code | B2 |
| Filing date | Dec 16, 2015 |
| Priority date | Dec 16, 2015 |
| Publication date | Jan 3, 2023 |
| Grant date | Jan 3, 2023 |
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Suggested is a composition with stabilized taste and/or odor, comprising (a) at least one acetophenone derivative of formula (I) wherein R 1 stands for hydrogen or methyl, and R 2 stands for hydrogen, hydroxyl or a —OCH 3 group, or a cosmetically pharmaceutically acceptable salt thereof, and (b) at least one mono- or polyunsaturated C 8 -C 22 fatty acid or its monohydric polyhydric C 1 -C 18 alkyl alcohols ester.
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What is claimed is: 1. A method for stabilizing the taste and/or odor of mono- or polyunsaturated C8-C22 fatty acid or its monohydric or polyhydric C 1 -C 18 aliphatic alcohol ester in a composition containing the same, comprising the steps of adding 4-hydroxyacetophenone to said mono- or polyunsaturated C 8 -C 22 fatty acid or its monohydric or polyhydric C 1 -C 18 aliphatic alcohol ester, in an amount effective to prevent oxidation and rancidity of said mono- or polyunsaturated C 8 -C 22 fatty acid or its monohydric or polyhydric C 1 -C 18 aliphatic alcohol ester, forming a composition containing both said 4-hydroxyacetophenone and said mono- or polyunsaturated C 8 -C 22 fatty acid or its monohydric or polyhydric C 1 -C 18 aliphatic alcohol ester, with said 4-hydroxyacetophenone present in an amount from 0.01 to 5 wt. %, based on the total weight of said composition, preventing oxidation and rancidity of said mono- or polyunsaturated C 8 -C 22 fatty acid or its monohydric or polyhydric C 1 -C 18 aliphatic alcohol ester for at least two months after forming said composition, and stabilizing said mono- or polyunsaturated C 8 -C 22 fatty acid or its monohydric or polyhydric C 1 -C 18 aliphatic alcohol ester for at least two months after forming said composition. 2. The method of claim 1 , wherein the mono- or polyunsaturated C 8 -C 22 fatty acid or its monohydric or polyhydric C 1 -C 18 alkyl alcohol ester comprises (b-1) at least one acyl compound of formula (II) wherein R stands for hydrogen atom or an C 1 -C 18 alkyl group, and X represents a mono- or polyunsaturated C 8 -C 22 acyl group, and/or (b-2) at least one acylglycerol compound of formula (III) wherein X′, X″ and X′″ independently of one another represents a hydrogen atom or a saturated or mono- or polyunsaturated C 8 -C 22 acyl group, with the proviso that X′, X″ and X′″ do not simultaneously represent a hydrogen atom and at least one of X′, X″ and X′″ being an unsaturated acyl group. 3. The method of claim 1 , where the added amount of 4-hydroxyacetophenone is from 0.05 to 2 wt. %, based on the total weight of the composition comprising both said 4-hydroxyacetophenone and said mono- or polyunsaturated C 8 -C 22 fatty acid or its monohydric or polyhydric C 1 -C 18 aliphatic alcohol ester. 4. The method of claim 3 , where the added amount of 4-hydroxyacetophenone is from 0.1 to 1 wt. %, based on the total weight of the composition comprising both said 4-hydroxyacetophenone and said mono- or polyunsaturated C 8 -C 22 fatty acid or its monohydric or polyhydric C 1 -C 18 aliphatic alcohol ester. 5. The method of claim 1 , wherein said fatty acid or ester is a blend of oleic, linoleic, palmitic and stearic acids. 6. The method of claim 1 , wherein said fatty acid or ester is a blend of oleic, linoleic, palmitic and palmitoleic acids. 7. The method of claim 1 , wherein said fatty acid or ester is a blend of oleic and linoleic acids. 8. The method of claim 1 , wherein said fatty acid is linoleic acid.
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