IP Library Granted Patent US 9,855,207
Granted Patent B2
US 9,855,207 · App. 13/979,411 · Granted Jan 2, 2018

UV-photo-protecting cosmetic composition

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Quick Facts
Patent No.
US 9,855,207
App. No.
13/979,411
Granted
Jan 2, 2018
Kind
B2
Abstract

The present invention relates to an UV-photo-protecting cosmetic composition, including: (a) at least one aqueous phase, (b) at least one fatty phase, (c) at least one micronized organic UV-screening agent, the mean particle size of said micronized particles ranging from 0.01 to 2 μm, and (d) at least one organomodified silicone which does not include poly(oxyalkylene) moieties.

Claims (75)

1. An UV-photo-protecting cosmetic composition, comprising:

(a) at least one aqueous phase,

(b) at least one fatty phase,

(c) at least one micronized organic UV-screening agent, the mean particle size of said micronized particles ranging from 0.01 to 2 μm, and

(d) at least one organomodified silicone which does not comprise poly(oxyalkylene) moieties, wherein

said at least one organomodified silicone has the following structural formula (I):

[M a D b T c Q d ] e   (I)

wherein

M=R 3 SiO 1/2 ,

D=R 2 SiO 2/2 ,

T=RSiO 3/2 ,

Q=SiO 4/2 ,

with

a=1-10

b=0-1000

c=0-1

d=0-1

e=1-10

wherein R=C 1 to C 22 -alkyl, fluoro-substituted C 1 to C 22 -alkyl, C 2 to C 22 -alkylene, or C 6 to C 20 aryl, which is bound to Si via a carbon atom,

with the requirement that at least one group R is replaced by at least one group R 11 and at least one group R 12 , wherein

R 11 =—Z-(E) y , wherein

E is

E 21 =—NR 4 R 5 ,

wherein R 4 and R 5 identical or different, selected from the group consisting of: hydrogen and straight chained, cyclic or branched, saturated or unsaturated C1 to C9 hydrocarbon radicals, optionally containing one or more groups selected from —O—, —NH—, —NR 3 , wherein R 3 =straight chained, cyclic or branched, saturated or unsaturated hydrocarbon radical with up to 6 carbon atoms, and —C(═O)—, and wherein the straight chained, cyclic or branched, saturated or unsaturated C1 to C9 hydrocarbon radicals are optionally substituted by one or more OH— and/or —NH 2 groups, and

E optionally comprises

E 11 =—O—C(═O)—R 21 ,

wherein R 21 = straight chained, cyclic or branched, saturated or unsaturated C1 to C6 hydrocarbon radicals, optionally containing one or more groups selected from —O—, —NH—, —NR 3 —, —C(═O)—, and wherein the straight chained, cyclic or branched, saturated or unsaturated C1 to C6 hydrocarbon radicals are substituted by one or more OH-groups, wherein R 3 = straight chained, cyclic or branched, saturated or unsaturated hydrocarbon radical with up to 6 carbon atoms, and

R 12 =—Z-(E) y , wherein

E =E 12 =—O—C(═O)—R 22 , wherein

R 22 = straight chained, cyclic or branched, saturated or unsaturated C7 to C22 hydrocarbon radical, optionally containing one or more groups selected from —O—, —NH—, —NR 3 —, wherein R 3 is as defined above, and —C(═O)—, and wherein straight chained, cyclic or branched, saturated or unsaturated C7 to C22 hydrocarbon radical is also optionally substituted by one or more OH-groups,

Z =a bivalent or trivalent straight-chained, cyclic or branched, saturated or unsaturated C2 to C20 hydrocarbon residue,

wherein Z optionally further comprises one or more groups selected from

*—O—**, *—NH—** and

wherein * and ** and *** denote bonds to different carbons in the C2 to C20 hydrocarbon residue,

and wherein Z is substituted by one or more —OH groups, or

wherein Z is a bivalent or trivalent straight-chained, cyclic or branched, saturated or unsaturated C2 to C20 hydrocarbon residue, and

y=1 or 2.

2. The UV-photo-protecting cosmetic composition of claim 1 , wherein the group Z comprises at least one residue selected from the group consisting of:

—(CH 2 ) z —wherein z is 1 to 10,

wherein x =1 -4.

3. The UV-photo-protecting cosmetic composition of claim 1 , wherein the group Z is a residue selected from the group of the formulas:

wherein * denotes the bond to the silicon atom and ** denotes the bond to the residue E.

4. The UV-photo-protecting cosmetic composition of claim 1 , wherein the at least one organomodified silicone (d) comprises structural elements selected from the following formulas:

wherein f=0-600,

wherein g=0-700,

wherein h=0-10,

wherein i=0-10,

wherein j=0-30,

wherein k=0-30,

wherein 1=0-10, and wherein f+g+h+i+j+k+l=12 to 1000.

5. The UV-photo-protecting cosmetic composition of claim 1 , wherein the residues R 11 are selected from the group consisting of:

and wherein the residues R 12 are selected from the group consisting of:

6. The UV-photo-protecting cosmetic composition of claim 1 , wherein the least one organomodified silicone free of poly(oxyalkylene) moieties is present in an amount of from 0.1% to 20% by weight.

7. The UV-photo-protecting cosmetic composition of claim 1 , wherein the micronized organic UV-screening agent is selected from the group consisting of an oxanilide, a triazine, a triazole, a vinylamide, a cinnamide, and combinations thereof.

8. The UV-photo-protecting cosmetic composition of claim 1 , wherein the micronized organic UV-screening agent is a triazine-based UV-screening agent.

9. The UV-photo-protecting cosmetic composition of claim 1 , wherein the fatty phase comprises synthetic or natural oils or fats.

10. The UV-photo-protecting cosmetic composition of claim 1 , wherein:

the at least one fatty phase (b) is present in an amount of 3-40% by weight,

the at least one micronized organic UV-screening agent (c) is present in an amount of 0.1 to 15% by weight, wherein the mean particle size of said micronized particles is from 0.01 to 2μm,

the at least one organomodified silicone (d) which does not comprise poly(oxyalkylene) moieties is present in an amount of 0.1 to 5% by weight, and

the composition further comprises 0 to 50% by weight of at least one auxiliary substance, and

sufficient water to bring the total formulation up to 100% by weight.

11. The UV-photo-protecting cosmetic composition of claim 1 , formulated as at least one of a cream, a milk, a gel, a lotion, an ointment, a gel cream, a suspension, a dispersion, a powder, a shampoo, a solid stick, a foam and a spray.

12. The UV-photo-protecting cosmetic composition of claim 2 , formulated as at least one of a cream, a milk, a gel, a lotion, an ointment, a gel cream, a suspension, a dispersion, a powder, a shampoo, a solid stick, a foam and a spray.

13. The UV-photo-protecting cosmetic composition of claim 3 , formulated as at least one of a cream, a milk, a gel, a lotion, an ointment, a gel cream, a suspension, a dispersion, a powder, a shampoo, a solid stick, a foam and a spray.

14. The UV-photo-protecting cosmetic composition of claim 4 , formulated as at least one of a cream, a milk, a gel, a lotion, an ointment, a gel cream, a suspension, a dispersion, a powder, a shampoo, a solid stick, a foam and a spray.

15. The UV-photo-protecting cosmetic composition of claim 5 , formulated as at least one of a cream, a milk, a gel, a lotion, an ointment, a gel cream, a suspension, a dispersion, a powder, a shampoo, a solid stick, a foam and a spray.

16. The UV-photo-protecting cosmetic composition of claim 5 , wherein

the residues R 11 are hydrophilic and have a logP (25° C.) of <0.5 and

the residues R 12 are lipophilic and have a logP (25° C.) of ≧0.5,

the logP values determined on the basis of the corresponding compounds H—R 11 and H—R 12 .

17. The UV-photo-protecting cosmetic composition of claim 1 , wherein the residues R 11 comprise:

and optionally comprise

E 11 =—O—C(═O)—R 21

wherein R 21 =straight chained, cyclic or branched, saturated or unsaturated C1 to C6 hydrocarbon radical, optionally containing one or more groups selected from —O—, —NH—, —NR 3 —, —C(═O)—, and substituted by one or more OH-Groups, wherein R 3 =straight chained, cyclic or branched, saturated or unsaturated hydrocarbon radical with up to 6 carbon atoms.

Assignments (5)
RELEASE OF SECURITY INTEREST Recorded Nov 11, 2020
From: JPMORGAN CHASE BANK, N.A., AS COLLATERAL AGENT
To: MOMENTIVE PERFORMANCE MATERIALS INC.
Reel/Frame 054336/0023 →
TERMINATION AND RELEASE OF SECURITY INTEREST IN PATENT RIGHTS Recorded Nov 20, 2014
From: JPMORGAN CHASE BANK, N.A.
To: MOMENTIVE PERFORMANCE MATERIALS INC.
Reel/Frame 034410/0607 →
SECURITY INTEREST Recorded Apr 22, 2014
From: MOMENTIVE PERFORMANCE MATERIALS INC.
To: JPMORGAN CHASE BANK, N.A., AS COLLATERAL AGENT
Reel/Frame 032736/0552 →
SECURITY INTEREST Recorded Apr 22, 2014
From: MOMENTIVE PERFORMANCE MATERIALS INC.
To: JPMORGAN CHASE BANK, N.A., AS COLLATERAL AGENT
Reel/Frame 032754/0774 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 28, 2013
From: MAASS, SEBASTIAN; WAGNER, ROLAND; SOCKEL, KARL-HEINZ; DAVIS, MARK; SCHNERING, ALBERT; STREICHER, KATHARINA
To: MOMENTIVE PERFORMANCE MATERIALS GMBH
Reel/Frame 031100/0213 →