Cosmetic Composition Comprising A Carboxy-Functional Elastomer

US2016199286A1 · US · A1

Patent metadata
FieldValue
Publication numberUS-2016199286-A1
Application numberUS-201414912183-A
CountryUS
Kind codeA1
Filing dateOct 29, 2014
Priority dateOct 31, 2013
Publication dateJul 14, 2016
Grant date

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  1. Title

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  2. Abstract

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  3. Assignees and inventors

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  4. Key dates

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  5. First independent claim

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Abstract

Official abstract text for this publication.

A cosmetic composition is provided that includes an elastomer and at least one cosmetic component optionally in a cosmetically acceptable medium. The elastomer is according to the general formula: A-B-A or B-A-B, wherein each A independently comprises a polysiloxane moiety having at least two siloxy (Si—O) groups and wherein each B independently comprises a moiety, or a precursor thereof, having at least two carboxyl groups and wherein B is bonded to a silicon atom in A.

First claim

Opening claim text (preview).

1 . A cosmetic composition comprising: (a) an elastomer according to the general formula: A-B-A or B-A-B, wherein each A independently comprises a polysiloxane moiety having at least two siloxy (Si—O) groups; wherein each B independently comprises a moiety, or a precursor thereof, having at least two carboxyl groups; and wherein B is bonded to a silicon atom in A; and (b) at least one cosmetic component; (c) optionally in a cosmetically acceptable medium. 2 . A cosmetic composition comprising: (a) an elastomer having at least two siloxy (Si—O) groups and at least two carboxyl groups, the elastomer comprising the reaction product of a reaction of: a first component having at least one reactive group; a second component having at least one reactive group; and a third component having at least two reactive groups reactive with the reactive groups of the first and second component for linking the first component to the second component; (b) at least one cosmetic component; and (c) optionally in a cosmetically acceptable medium. 3 . The cosmetic composition according to claim 2 , wherein the at least one reactive component of the first component and the second component are independently selected from a hydroxyl group or an amine group and wherein the at least two reactive groups of the third component are anhydride groups. 4 . The cosmetic composition according to claim 3 wherein the first and second component are selected from siloxanes having at least one hydroxyl group or organic alcohols having at least one hydroxyl group and the third component a siloxane having at least two terminal anhydride groups, or the first and second component are selected from siloxanes having at least one amine group or organic amines having at least one amine group and the third component a siloxane having at least two pendant anhydride groups. 5 . (canceled) 6 . The cosmetic composition according to claim 2 , wherein the at least one reactive component of the first component and the second component are anhydride groups and wherein the at least two reactive groups of the third component are hydroxyl groups or amine groups. 7 . The cosmetic composition according to claim 6 wherein the first and second component are siloxanes and the anhydride groups are pendant. 8 . The cosmetic composition according to claim 6 wherein the third component is selected from i) an organic polyol having at least two hydroxyl groups; ii) a third siloxane having at least two hydroxyl groups; iii) an organic polyamine having at least two amine groups; or iv) a third siloxane having at least two amine groups. 9 . The cosmetic composition according to claim 1 or claim 2 wherein the elastomer is according to the general formula: wherein each of R 1 , R 4 , R 5 , R 11 , R 14 , and R 15 is independently a substituted or unsubstituted hydrocarbyl group, each of w and ww is an independently an integer from zero (0) to 1,000, each of x and xx is an independently an integer from 1 to 100, each of y and yy is an independently an integer from 0 to 1,000, and X is of the following general formula: wherein each Y is a divalent group and wherein each of R 3 and R 13 is independently a divalent group; or according to the general formula: wherein each of R 1 , R 4 , R 5 , R 11 , R 14 , and R 15 is independently a substituted or unsubstituted hydrocarbyl group, each of w and ww is an independently an integer from zero (0) to 1,000, each of x and xx is an independently an integer from 1 to 100, each of y and vv is an independently an integer from 0 to 1,000, and X 2 is of the following general formula: wherein each Y 2 is an divalent group and wherein each R is independently a hydrogen atom (H) or R 1 and wherein each of R 3 and R 13 is independently a divalent group; or according to the general formula: wherein each of R 8 , R 10 , R 11 , R 18 , R 20 , and R 21 is independently a substituted or unsubstituted hydrocarbyl group, each of a and aa is an independently selected integer from zero (0) to 1,000, each of b and bb is an independently selected integer from 1 to 1000, each of c and cc is an independently selected integer from 0 to 1,000, and X 3 is of the following general formula: wherein each Y 3 is of the following formula: —SiR 5 2 —O—[SiR 1 R 4 —O—] w [SiR 1 R 2 —O—] x [SiR 1 R 4 —O—] y SiR 5 2 —; wherein each of R 1 , R 2 , R 4 , and R 5 is independently a substituted or unsubstituted hydrocarbyl group; each of Z, R 3 , and R 13 is independently a divalent group; each d is independently 0 or 1; w is an integer selected from 0 to 1,000: x is an integer selected from 0 to 100, and y is an integer selected from 0 to 1,000; or according to the general formula: wherein each of R 8 , R 10 , R 11 , R 18 , R 20 , and R 21 is independently a substituted or unsubstituted hydrocarbyl group, each of a and aa is an independently selected integer from zero (0) to 1,000, each of b and bb is an independently selected integer from 1 to 1000, each of c and cc is an independently selected integer from 0 to 1,000, and X 4 is of the following general formula: wherein each Y 4 is of the following formula: —SiR 5 2 —O—[SiR 1 R 4 —O—] w [SiR 1 R 2 —O—] x [SiR 1 R 4 —O—] y SiR 5 2 —; wherein each of R 1 , R 2 , R 4 , and R 5 is independently a substituted or unsubstituted hydrocarbyl group; each of Z, R 3 , and R 13 is independently a divalent group; each R is independently a hydrogen atom (H) or R 1 ; each d is independently 0 or 1; w is an integer selected from 0 to 1,000; x is an integer selected from 0 to 100, and y is an integer selected from 0 to 1,000. 10 .- 12 . (canceled) 13 . The cosmetic composition according to claim 1 wherein the elastomer is according to the general formula: wherein each Y 5 is of the following formula: —SiR 5 2 —O—[SiR 1 R 4 —O—] w [SiR 1 R 2 —O—] x [SiR 1 R 4 —O—] y SiR 5 2 —; wherein each of Z 1 and Z 2 is independently attributable to an organic alcohol having at least one hydroxyl group, each of R 3 and R 13 is independently a divalent group, each of R 1 , R 2 , R 4 , and R 5 is independently a substituted or unsubstituted hydrocarbyl group, w is an integer selected from zero (0) to 1,000, x is an integer selected from 0 to 100, and y is an integer selected from 0 to 1,000; or according to the general formula:

Assignees

Inventors

Classifications

  • for lips · CPC title

  • containing inorganic ingredients · CPC title

  • Mucopolysaccharides, e.g. hyaluronic acid; Derivatives thereof · CPC title

  • Preparations for cleaning the hair · CPC title

  • At least two compounds being classified in the same subclass of A61K8/18 · CPC title

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What does patent US2016199286A1 cover?
A cosmetic composition is provided that includes an elastomer and at least one cosmetic component optionally in a cosmetically acceptable medium. The elastomer is according to the general formula: A-B-A or B-A-B, wherein each A independently comprises a polysiloxane moiety having at least two siloxy (Si—O) groups and wherein each B independently comprises a moiety, or a precursor thereof, havin…
Who is the assignee on this patent?
Dow Corning
What technology area does this patent fall under?
Primary CPC classification A61K8/894. Mapped technology areas include Human Necessities.
When was this patent published?
Publication date Thu Jul 14 2016 00:00:00 GMT+0000 (Coordinated Universal Time) (A1). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).