GB2074184A - Compositions for Treating Hair and Other Fibrous Materials - Google Patents

Compositions for Treating Hair and Other Fibrous Materials Download PDF

Info

Publication number
GB2074184A
GB2074184A GB8111208A GB8111208A GB2074184A GB 2074184 A GB2074184 A GB 2074184A GB 8111208 A GB8111208 A GB 8111208A GB 8111208 A GB8111208 A GB 8111208A GB 2074184 A GB2074184 A GB 2074184A
Authority
GB
United Kingdom
Prior art keywords
composition
weight
detergent
hair
compositions
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
GB8111208A
Other versions
GB2074184B (en
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Dow Silicones UK Ltd
Original Assignee
Dow Corning Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Dow Corning Ltd filed Critical Dow Corning Ltd
Priority to GB8111208A priority Critical patent/GB2074184B/en
Publication of GB2074184A publication Critical patent/GB2074184A/en
Application granted granted Critical
Publication of GB2074184B publication Critical patent/GB2074184B/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16Organic compounds
    • C11D3/37Polymers
    • C11D3/3703Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • C11D3/373Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds containing silicones
    • C11D3/3734Cyclic silicones
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/33Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
    • A61K8/34Alcohols
    • A61K8/342Alcohols having more than seven atoms in an unbroken chain
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/33Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
    • A61K8/39Derivatives containing from 2 to 10 oxyalkylene groups
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/58Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing atoms other than carbon, hydrogen, halogen, oxygen, nitrogen, sulfur or phosphorus
    • A61K8/585Organosilicon compounds
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q5/00Preparations for care of the hair
    • A61Q5/02Preparations for cleaning the hair

Abstract

A detergent composition, particularly for use as a hair shampoo, consisting of a detergent substance, for example one based on a fatty alcohol or a fatty alcohol ethoxylate, and from 0.5 to 20 per cent by weight, based on the total composition, of a cyclic methyl siloxane. The presence of the cyclic siloxane results in reduced drying time of the washed fibres.

Description

SPECIFICATION Compositions for Treating Hair and Other Fibrous Materials This invention relates to compositions for use as shampoos for hair and other fibrous materials.
It is known to employ certain silicones as additives to hair treating compositions such as hair conditioning agents. It has also been disclosed in U.S. Patent 2 826 551 that the addition of a liquid linear polysiloxane to a hair shampoo results in the treated hair having a reduced tendency to tangle.
The operative liquid linear silicones are stated therein to be non-volatile under normal use conditions and to have a preferred viscosity of at least 100 cS at 250C. Further disclosure of the addition of silicones to hair shampoos occurs in U.K. Patent Specification No. 849 433 which discloses that polymerised dimethyl and diethyl silanediols having viscosities within the range from 1.0 to 2,500,000 centistokes may be incorporated into detergent compositions. The said specification states that use of the detergent compositions as hair washing preparations decreases the length of time required to dry the hair after shampooing. However, according to tests that we have carried out, the decrease in drying time obtained with the described polymerised diols, e.g. those having viscosities of about 300 cS, is relatively small.There has therefore remained a need for a hair washing preparation having a significantly reduced drying time following the shampooing step.
According to this invention there is provided a detergent composition which is particularly adapted to the washing of hair and other natural and/or synthetic fibrous materials, the said composition comprising one or more detergent substances and from 0.5 to 20% by weight, based on the total weight of the composition, of at least one cyclic siloxane represented by the general formula
in which n has a value of from 3 to 6 inclusive.
The detergent substance employed in the compositions of this invention may be any of those which find application in the shampooing of hair and other fibrous materials. Such detergent substances include the fatty acid soaps, alkyl benzene sulphonates, alkyl sulphates, alkyl ether suiphates, monoglyceride sulphates, alkyl phosphates, methyl taurides and the fatty acid alkanolamides.When the detergent composition is intended for use as a shampoo for the hair of humans or animals the preferred detergent substances are those based on fatty alcohols or fatty alcohol ethoxylates, particularly those derived from lauryl and myristyl alcohol, and their salts, for example sodium lauryl sulphate, sodium lauryl ether sulphate, ammonium lauryl sulphate, triethanolamine lauryl sulphate, monoethanolamine lauryl sulphate, disodium lauryl ethoxy sulphosuccinate and disodium cocomonoethanolamide ethoxy sulphosuccinate. The concentration of the detergent component in the composition can vary widely depending on the type of shampoo product required.For most conventional shampoo applications, however, the detergent is normally present in the end-product in a proportion of from 7.5% to 50% (preferably 1025%) by weight, the remainder being water and other additives such as foam stabilisers, preservatives and perfumes.
The siloxane component of the compositions of this invention comprises one or more cyclic siloxanes which can be represented by the general formula set out hereinabove. Specifically, the cyclic siloxa nes are respectively hexa methylcyclotrisiloxane, octa methylcyclotetrasiloxane, decamethylcyclopentasiloxane and dodecamethylcyclohexasilane. Compared with the linear polydimethylsiloxanes the cyclic siloxanes employed according to this invention are relatively volatile materials having boiling points below about 2500C at 760 mm Hg. The cyclic siloxanes may be employed as the individual compounds or as mixtures of two, three, or all four. The trisiloxane in its pure form is a solid at just below normal room temperature.It is therefore preferred that it be employed as a mixture with a higher cyclic siloxane, for example the tetrasiloxane or pentasiloxane or both.
From 0.5 to 20% by weight of the cyclic siloxane is employed to prepare the compositions of this invention, the preferred proportion being from about 2% to 10% by weight, based on the total weight of the composition. Dispersion of the cyclic siloxane in the shampoo composition can be achieved by any convenient procedure, for example by adding the siloxane per se to the finished shampoo composition with vigorous stirring. More preferably however the siloxane is emulsified prior to incorporation into the composition.
In addict on to the two essential ingredients the compositions of this invention may contain other substances generally present in detergent compositions. For example, the composition may be thickened if desired by the addition of known viscosity increasing agents such as sodium chloride, cetyl alcohol, linoleic diethanolamide and cellulosic thickeners such as hydroxyethyl cellulose. Foam stabilising agents may also be incorporated, examples of such agents being coconut diethanolamide, lauric isopropanolamide, alkyl dimethyl betaine, alkyl dimethyl amine oxide and silicone-glycol copolymers. Additional ingredients which may normaliy be present include preservatives, such as formalin, pearlising agents, stearates and waxes, pH modifiers, colorants and perfumes. Conventional conditioning agents may also be incorporated.However, the cyclic siloxanes themselves are effective hair conditioning agents and it has been found that hair which has been shampooed with the compositions of this invention generally possesses gloss and ease of combing.
The following examples, in which the parts are expressed by weight, illustrate the invention: Example 1 A mixture of cyclic methyl siloxanes consisting of about 70% by weight of decamethylcyclopentasiloxane and about 25% by weight of dodecamethylcyclohexasiloxane, the remainder being the cyclotetra- and cyclotri-siloxanes, was emulsified in its own weight of water employing a non-ionic emulsifying agent.Two parts of the emulsion was then incorporated with vigorous stirring into eight parts of a hair shampoo (sold by Boots under the name Rosemary and believed to contain a fatty alcohol- or fatty alcohol ethoxylate- derived detergent) to give a detergent composition (Composition A) according to this invention Composition A and a control composition (no siloxane) were employed to shampoo switches of human hair, each approximately 30 cm in length and weighing 30 g. Each switch was shampooed by immersion in water at 300C containing 4% by weight of the detergent composition. After immersion for about 10 seconds the switch was removed and rubbed between the hands for about 20 seconds.
This wash procedure was performed three times and the switch finally rinsed free of suds. Excess rinse water was squeezed manually from the switch which was then weighed and dried by gentle heat from a warm air source. Further weighings were performed during the drying period. From graphs of the results the times required for the switches to lose 25, 50, 75 and 90% by weight of their immediate post wash water content were ascertained.
The above described procedure was repeated except that instead of the cyclic siloxanes there was added an equal proportion of a trimethylsiloxy-terminated polydimethylsiloxane having a viscosity of 100 cS at 25%C. The composition was designated Composition B and its control (no siloxane) was designated Control B.
The results obtained for Compositions A and B and the controls were as follows:
Time (min.) Composition Control Composition Control % WaterLost A A B B 0 0 0 0 0 25 5 8 9 12 50 11 14 21 28 75 21 29 45 57 90 38 55 65 71 Example 2 The procedure of Example 1 was repeated except that as the cyclic siloxane there was employed a mixture containing about 84% by weight of octamethylcyclotetrasiloxane and about 1 6% by weight of decamethylcyclopentasiloxane.Hair washed with the shampoo containing the cyclic siloxane dried more quickly than hair washed with the same shampoo to which no siloxane had been added or to which 100 cS polydimethylsiloxane had been added in place of the cyclic siloxane.
Example 3 A pearlised shampoo composition was prepared by mixing: sodium lauryl ether sulphate (28% solution in water) 40 parts pearlising agent (Empicol 0627) 8 parts coconut diethanolamide 3 parts thickening agent qs citric acid to pH 6.5-7.0 water balance to 100 parts To the shampoo composition (9 parts) was added, with stirring, the emulsified mixture (1 part) of cyclic siloxanes employed in Example 1. The resulting composition was then used to shampoo switches of human hair (30 g) each being washed twice for a period of about 20 seconds with a 20% by weight solution of the shampoo in water (450C). The hair was rinsed in warm water after each wash.
Following the second rinse excess water was squeezed out manually, the switches were weighed and then placed in a current of warm air (about 700C) until dry. The loss of weight was monitored periodicaliy during drying and the data employed to determine the time required for the switches to lose 25, 50, 75 and 90% by weight of their immediate post wash water content. The procedure was repeated using a control shampoo (no siloxane) and the times recorded for the siloxane-modified shampoo were expressed as a percentage of the corresponding drying times for the control. At all stages of water loss the use of the siloxane-modified shampoo resulted in a shorter drying time than the control, as follows:
% by weight of % time required water lost versus control 25 71.8 50 73.4 75 80.3 90 80.5

Claims (8)

Claims
1. A liquid detergent composition comprising one or more detergent substances and from 0.5 to 20 per cent by weight, based on the total weight of the composition, of at least one cyclic siloxane represented by the general formula:
in which n has a value of from 3 to 6 inclusive.
2. A composition as claimed in Claim 1 wherein the detergent substance is based on a fatty alcohol or a fatty alcohol ethoxylate.
3. A composition as claimed in any one of the preceding claims wherein the detergent substance is present in an amount of from 10 to 25 per cent by weight based on the total weight of the composition.
4. A composition as claimed in Claim 1 or Claim 2 wherein the cyclic siloxane is present in an amount of from 2 to 10 per cent by weight based on the total weight of the composition.
5. A composition as claimed in any one of the preceding claims wherein the cyclic siloxane has been incorporated in an aqueous emulsion.
6. A composition as claimed in Claim 1 substantially as described with reference to the Examples.
7. A process for shampooing a fibrous material which comprises applying thereto a composition as claimed in any one of the preceding claims.
8. A process as claimed in Claim 7 wherein the fibrous material is human or animal hair.
GB8111208A 1980-04-19 1981-04-09 Compositions for treating hair and other fibrous materials Expired GB2074184B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB8111208A GB2074184B (en) 1980-04-19 1981-04-09 Compositions for treating hair and other fibrous materials

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GB8012933 1980-04-19
GB8111208A GB2074184B (en) 1980-04-19 1981-04-09 Compositions for treating hair and other fibrous materials

Publications (2)

Publication Number Publication Date
GB2074184A true GB2074184A (en) 1981-10-28
GB2074184B GB2074184B (en) 1983-06-02

Family

ID=26275239

Family Applications (1)

Application Number Title Priority Date Filing Date
GB8111208A Expired GB2074184B (en) 1980-04-19 1981-04-09 Compositions for treating hair and other fibrous materials

Country Status (1)

Country Link
GB (1) GB2074184B (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0182583A2 (en) * 1984-11-13 1986-05-28 Dow Corning Corporation Method for cleaning textiles with cyclic siloxanes
FR2629714A1 (en) * 1988-04-07 1989-10-13 Dow Corning Ltd TRANSPARENT SHAMPOO COMPOSITION, PROCESS FOR PRODUCING THE SAME, AND PROCESS FOR USE IN TREATING HAIR
EP0351185A2 (en) * 1988-07-11 1990-01-17 Colgate-Palmolive Company Silicone-based hard surface cleaner
US4911919A (en) * 1986-06-17 1990-03-27 Colgate-Palmolive Company Hair straightening conditioner
US5213793A (en) * 1984-01-13 1993-05-25 The Gillette Company Hair conditioning

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
USRE34584E (en) 1984-11-09 1994-04-12 The Procter & Gamble Company Shampoo compositions
US6322778B1 (en) 1998-02-10 2001-11-27 Johnson & Johnson Consumer Companies, Inc. Hair conditioning compositions comprising a quaternary ammonium compound

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5213793A (en) * 1984-01-13 1993-05-25 The Gillette Company Hair conditioning
EP0182583A2 (en) * 1984-11-13 1986-05-28 Dow Corning Corporation Method for cleaning textiles with cyclic siloxanes
EP0182583A3 (en) * 1984-11-13 1988-04-06 Dow Corning Corporation Method for cleaning textiles with cyclic siloxanes
US4911919A (en) * 1986-06-17 1990-03-27 Colgate-Palmolive Company Hair straightening conditioner
FR2629714A1 (en) * 1988-04-07 1989-10-13 Dow Corning Ltd TRANSPARENT SHAMPOO COMPOSITION, PROCESS FOR PRODUCING THE SAME, AND PROCESS FOR USE IN TREATING HAIR
EP0351185A2 (en) * 1988-07-11 1990-01-17 Colgate-Palmolive Company Silicone-based hard surface cleaner
EP0351185A3 (en) * 1988-07-11 1990-10-24 Colgate-Palmolive Company Silicone-based hard surface cleaner
AU625658B2 (en) * 1988-07-11 1992-07-16 Colgate-Palmolive Company, The Silicone-based hard surface cleaner

Also Published As

Publication number Publication date
GB2074184B (en) 1983-06-02

Similar Documents

Publication Publication Date Title
US4337166A (en) Compositions for treating hair and other fibrous materials
CA1196575A (en) Compositions used to condition hair
US4886660A (en) Shine hair conditioner
FI83474B (en) SHAMPOOKOMPOSITIONER.
US5049377A (en) Hair-care composition and methods of treating hair
CA2031382C (en) Hair treatment composition
US2826551A (en) Nontangling shampoo
US4933176A (en) Clear shampoo compositions
CA1245560A (en) Compositions and process for treating hair
CA1272959A (en) Shampoo compositions
US3816616A (en) Unitary shampoo and cream rinse compositions
US4818523A (en) Hair rinse conditioner
JPS621363B2 (en)
EP0275707A2 (en) Hair care composition containing modified aminoalkyl substituted polydiorganosiloxane
JPS61109707A (en) Conditioning shampoo
CS97491A3 (en) Hair shampoo preparation
US4777037A (en) Hair conditioning compositions containing volatile cyclic silicone and quaternary nitrogen-containing agent
US5554313A (en) Conditioning shampoo containing insoluble, nonvolatile silicone
CA1138341A (en) Waving composition from a reducing agent and cationic polymer
MXPA97003648A (en) Methods and compositions for the conditioning of the skin and the head
JPH04108725A (en) Hair cosmetic
EP0166232A2 (en) Foaming hair cleanser and conditioner
GB2074184A (en) Compositions for Treating Hair and Other Fibrous Materials
RU2248786C2 (en) Application of specific aminosilicones for treating keratin fibers before and after decolorization
JPS6025910A (en) Low ph hair treatment agent and neutral hair treatment composition containing amine oxide

Legal Events

Date Code Title Description
PCNP Patent ceased through non-payment of renewal fee

Effective date: 19930409