Organopolysiloxane gels

Patent metadata

Field	Value
Publication number	US-9657160-B2
Application number	US-201314394748-A
Country	US
Kind code	B2
Filing date	Apr 11, 2013
Priority date	Apr 16, 2012
Publication date	May 23, 2017
Grant date	May 23, 2017

Abstract

Organopolysiloxane gels produced by crosslinking an unsaturated organopolysiloxane resin with a crosslinking agent in the presence of a diluent have excellent sensory properties such as properties desirable in a variety of cosmetics products.

First claim

The invention claimed is:

1. An organopolysiloxane gel produced by a process comprising reacting:
(1) at least one unsaturated MQ resin comprising units of the formulas
SiO 2 (Q units) and
R 3 SiO 1/2 and R 2 R′SiO 1/2 (M units),

wherein
R is an identical or different monovalent, optionally substituted hydrocarbon group having 1 to 18 carbon atoms per group,
R′ is a monovalent hydrocarbon group capable of hydrosilylation by Si—H groups, with the provisos that the at least one unsaturated MQ resin contains at least 2 R′ groups that the molar ratio of M units to Q units is in a range from 0.5 to 4.0, and the at least one unsaturated MQ resin comprises (CH 3 ) 3 SiO 1/2 groups,
with
(2) at least one Si—H functional organopolysioxane of the formula
H c R 3−c SiO(R 2 SiO) a (RHSiO) b SiR 3−c H c   (I),

wherein
c is 0 or 1,
R is an identical or different monovalent, optionally substituted hydrocarbon group having 1 to 18 carbon atoms per group,
a and b are integers,
with the proviso
that the sum a+b is 66 to 248,
that the at least one Si—H functional organopolysiloxane of the formula (I) contains Si-bonded hydrogen in an amount from 0.011 to 0.044 wt. %, and
that the number of Si—H groups per molecule on average is greater than 2,
or a mixture of (2) the at least one Si—H functional organopolysiloxane of the formula (I) with
(2′) Si—H functional organopolysiloxanes of the formula
H c R 3−c SiO(R 2 SiO) a (RHSiO) b SiR 3−c H c   (I′),

wherein
c is 0 or 1,
R is an identical or different monovalent, optionally substituted hydrocarbon group having 1 to 18 carbon atoms per group,
a and b are integers,
with the proviso that the sum a+b is 38 to 248, that the Si—H functional organopolysiloxanes of the formula (I′) contain Si-bonded hydrogen in an amount from 0.045 to 0.35 wt. %, and that if a mixture of (2) and (2′) is used, the weight ratio of (2) to (2′) is greater than 0.2,
in the presence of
(3) a catalyst which promotes addition at Si-bonded hydrogen onto an aliphatic multiple bond,
wherein a mixture of (1) and (2) or a mixture of (1), (2), and (2′) is dispersed in
(4) at least one diluent selected from organopolysiloxanes with 2 to 200 Si atoms and organic diluents.

2. The organopolysiloxane gel of claim 1 , wherein the form of a creamy gel that is stable in storage.

3. The organopolysiloxane gel of claim 2 , wherein the organopolysiloxane gel further comprises at least one selected from the group consisting of active subatances for body care and active substance for health care.

4. The organopolysiloxane gel of claim 1 , wherein the at least one diluents is selected from the group consisting of polydimethylsiloxane having 2 to 50 Si atoms, aliphatic hydrocarbons having 4 to 30 carbon atoms, alicyclic hydrocarbons having 4 to 30 carbon atoms, and esters of carboxylic acids having 2 to 30 carbon atoms.

5. A method of producing the organopolysiloxane gel of claim 1 comprising reacting
(1) the at least one unsaturated MQ resin with
(2) the at least one Si-H functional organopolysiloxane of the formula (I) or
with a mixture of (2) the at least one Si—H functional organopolysiloxane of the formula (I) and (2′) the Si—H functional organopolysiloxane of the formula (I′),
in the presence of (3) a catalyst which promotes addition at Si-bonded hydrogen onto an aliphatic multiple bond, and
dispersing a mixture of (1) and (2) or a mixture of (1), (2), and (2′) in (4) at least one diluent selected from organopolysiloxane having 2 to 200 Si atoms and organic diluents.

6. The method of claim 5 further comprising homogenizing the organopolysiloxane gel after the reaction, and obtaining a creamy organopolysiloxane gel that is stable in storage.

7. The method of claim 6 further comprising diluting the organopolysiloxane gel with active substances for body care, active substances for health care, and/or the at least one diluent selected from organopolysiloxane having 2 to 200 Si atoms and organic diluents to form a diluted organopolysiloxane gel, and optionally homogenizing the diluted organopolysiloxane gel.

8. The method of claim 7 , wherein the at least one diluent is selected from the group consisting of polydimethylsiloxane having 2 to 50 Si atoms, aliphatic hydrocarbons having 4 to 30 carbon atoms, alicyclic hydrocarbons having 4 to 30 carbon atoms, and esters of carboxylic acids having 2 to 30 carbon atoms.

9. A cosmetic composition comprising one or more organopolysiloxane gels of claim 1 .

10. A cosmetic composition comprising one or more organopolysiloxane gels as produced in claim 5 .

11. The organopolysiloxane gel of claim 1 , wherein R′ is a terminal alkenyl group having 2 to 12 carbon atoms.

12. The organopolysiloxane gel of claim 1 , wherein R′ is a vinyl group.

13. The organopolysiloxane gel of claim 1 , wherein the at least one unsaturated MQ resin contains at least 3 R′ groups and the molar ratio of M units to Q units is in a range from 0.5 to 2.0.

14. The organopolysiloxane gel of claim 1 , wherein the sum a+b is from 118 to 168.

15. The organopolysiloxane gel of claim 1 , wherein the at least one Si—H functional organopolysiloxane of the formula (I) contains Si-bonded hydrogen in an amount from 0.022 to 0.032 wt. %.

16. The organopolysiloxane gel of claim 1 , wherein the Si—H functional organopolysiloxanes of the formula (I′) contain Si-bonded hydrogen in an amount from 0.045 to 0.156 wt. %.

17. The organopolysiloxane gel of claim 1 , wherein the weight ratio of (2) to (2′) is greater than 0.3.

18. The method of claim 5 , wherein R′ is a terminal alkenyl having 2 to 12 carbon atoms.

19. The method of claim 5 , wherein R′ is a vinyl group.

Assignees

• Wacker Chemie Ag

Inventors

• Knoer Sebastian
• Roy Aroop Kumar

Classifications

• A61Q1/02 Primary

  Preparations containing skin colorants, e.g. pigments (preparations in powder form A61Q1/12) · CPC title

• C08K5/548 Primary

  containing sulfur {(C08K5/5477 takes precedence)} · CPC title

• C08K5/56

  Organo-metallic compounds, i.e. organic compounds containing a metal-to-carbon bond · CPC title

• C08G77/12

  containing silicon bound to hydrogen · CPC title

• C08K5/5403

  containing no other elements than carbon or hydrogen · CPC title