COSMETIC COMPOSITIONS FOR COMBATTING COLOUR LOSS FROM A DYED MATERIAL

20190231664 ยท 2019-08-01

Assignee

Inventors

Cpc classification

International classification

Abstract

A concentrate composition comprising: (a) at least 0.1 wt % of a surfactant compound; and (b) at least 10 wt % one or more ingredients selected from aldehydes, succinimidyl esters, chelating agents and amine salts of carboxylic acids.

Claims

1. A concentrate composition comprising: (a) at least 0.1 wt % of a surfactant compound; and (b) at least 10 wt % of one or more ingredients selected from the group consisting of aldehydes, succinimidyl esters, chelating agents and amine salts of carboxylic acids; wherein component (b) comprises an aldehyde, a chelating agent and an amine salt of a carboxylic.

2. The concentrate composition according to claim 1 wherein component (b) comprises an aldehyde selected from the group consisting of -substituted aldehydes, hydroxy-substituted aldehydes and combinations thereof.

3. The concentrate composition according to claim 1 wherein the aldehyde is 2-hydroxyoctanal.

4. The concentrate composition according to claim 1 wherein component (b) comprises a polycarboxylic acid derived chelating agent.

5. The concentrate composition according to claim 1 wherein the chelating agent is glutamic acid N,N-diacetic acid (GLDA) and/or diethylene triamine pentaacetic acid (DTPA).

6. The concentrate composition according to claim 1 wherein component (b) comprises a salt of a monocarboxylic acid and a secondary or tertiary amine.

7. The concentrate composition according to claim 1 wherein component (b) comprises triethanolamine salt of octanoic acid.

8. The concentrate composition according to claim 1 wherein component (a) is selected from the group consisting of sodium laureth sulfate (SLES), cocamidopropyl betaine (CAPB), and mixtures thereof.

9. The concentrate composition according to claim 1 which comprises cocamidopropyl betaine (CAPB), 2-hydroxyoctanol, glutamic acid N,N-diacetic acid (GLDA) and the triethanolamine salt of octanoic acid.

10. The concentrate composition according to claim 1 wherein components (a) and (b) together comprise at least 20 wt % of the composition.

11. The concentrate composition according to claim 1 wherein component (a), component (b) and water together comprise at least 90 wt % of the composition.

12. The concentrate composition according to claim 1 which is in the form of a stable emulsion.

13. (canceled)

14. The concentrate composition according to claim 1 which comprises 0.5 to 5 wt % of a surfactant compound, from 2 to 10 wt % of an aldehyde, from 5 to 25 wt % of a chelating agent and from 3 to 15 wt % of an amine salt of a carboxylic acid.

15. A formulated composition comprising a concentrate composition according to claim 1 and one or more further components.

16. A method of preparing a formulated composition, the method comprising admixing a concentrate composition as defined in claim 1 with one or more further components.

17. A formulated composition according to claim 15 wherein the formulated composition is a hair care composition.

18. A formulated composition according to claim 15 which provides one or more benefits selected from the group consisting of increased gloss or shine, improved combability, improved strength, increased softness, reduced protein loss, improved thermal durability, increased chemical resistance, increased waviness and increased straightness; wherein the benefit may be temporary, semi-permanent or permanent.

19.-20. (canceled)

21. The method according to claim 16 wherein the formulated composition is a hair care composition.

22. The method according to claim 16 which provides one or more benefits selected from the group consisting of increased gloss or shine, improved combability, improved strength, increased softness, reduced protein loss, improved thermal durability, increased chemical resistance, increased waviness and increased straightness; wherein the benefit may be temporary, semi-permanent or permanent.

Description

EXAMPLE 1

[0346] Compositions were prepared comprising the following components:

TABLE-US-00001 Wt % as active in formulation Formulation 1 2 3 4 5 6 7 8 9 Na.sub.4 16.7 20.0 13.4 16.7 16.7 20.0 16.7 20.0 23.4 GLDA.sup.1 2 hydroxy 5.0 6.0 4.0 5.0 5.0 6.0 5.0 6.0 7.0 octanal Triethanol- 7.5 9.0 6.0 7.5 7.5 9.0 7.5 9.0 10.5 amine salt of octanoic acid CAPB .sup.2 0.0 0.0 1.5 2.3 2.8 3.3 3.3 4.0 4.6 Water QS to 100 wt % .sup.1Added as Dissolvine GL-38 (38 wt % Na.sub.4GLDA) .sup.2 Added as Empigen BS/H50 (35 wt % cocoamidopropyl betaine)

EXAMPLE 2

[0347] Formulations 1 to 9 were stored for 48 hours at 25 C. and visually assessed. A stable system was a clear single phase.

[0348] Formulations 1 and 2 were unstable after 48 hours whereas formulations 3 to 9 were all stable.

EXAMPLE 3

[0349] Formulation 7 was stored for 4 months under ambient conditions (20-25 C., 1 atm). It remained stable after this period.