CN1120701C - Hair conditioning compositions comprising water-insoluble high molecular weight oily compound - Google Patents
Hair conditioning compositions comprising water-insoluble high molecular weight oily compound Download PDFInfo
- Publication number
- CN1120701C CN1120701C CN 96180564 CN96180564A CN1120701C CN 1120701 C CN1120701 C CN 1120701C CN 96180564 CN96180564 CN 96180564 CN 96180564 A CN96180564 A CN 96180564A CN 1120701 C CN1120701 C CN 1120701C
- Authority
- CN
- China
- Prior art keywords
- alkyl
- acylamino
- acid
- hair
- ethyl
- 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.)
- Expired - Fee Related
Links
Landscapes
- Cosmetics (AREA)
Abstract
The present invention discloses a hair regulation composition whose formula (I) is shown in the specification. The hair regulation composition comprises a water insoluble oily composition with high molecular weight and carriers. The water insoluble oily composition with high molecular weight has the molecular weight of at least 800 and the specific weight of at least about 0.9, is in liquid state at 25 DEG C, and is specified by formula (I) in which A<1>, a<2>, a<3> and A<4> can independently be alkyl, alkenyl, aryl, alkaryl, hydroxyalkyl alkoxyl group, alkoxyalkyl, acyl group or alkyl acyloxy whose carbon atom number ranges from 1 to 30, or is specified by the formula of-(CH2)n-O-OCR, wherein R refers to an alkyl or an alkenyl which has branched chains or straight chains, and has 1 to 30 carbon atoms, and n refers to an integer ranging from 1 to 30.
Description
Technical field
The present invention relates to a kind of Wo 2008069000 that comprises water-insoluble high molecular weight oily compound.
People's hair is because normal contact with external environment and owing to the scalp sebum secreted makes hair dirty.Hair is dirty just a kind of unclean or oily sensation, and appearance loses aesthetic feeling.Therefore hair needs often to clean.
Hair washing is to clean hair by removing dirt and too much sebum.But hair washing can make hair be in a kind of humidity, tangle, normally a kind of state that is difficult for combing.In case hair has been done, often be in a kind of drying, coarse, the matt or state that curls again, this is because natural oil, other natural conditioning and the moist composition of hair removed in hair washing.Static content also increased when hair was dry, disturbed combing, caused " hair dances in the air ", perhaps produced undesirable " terminal bifurcated " phenomenon, particularly for long hair.
People have developed several different methods and have alleviated the problem that occurs after the above-mentioned hair washing.These methods comprise from the hair conditioner of the back coating of having one's hair wash such as retained type (leave-on) product and rinsing type (rinse-off) product to attempting to clean hair conditioning shampoo with conditioning hair simultaneously by single product.Although shampoo simple and convenient of conditioner liked including by some consumers, but most of consumer still prefers traditional conditioner composition, these conditioner compositions are to use in the step of separating with the hair washing process, normally use after hair washing.The product form of conditioner can be retained type product or rinsing type product, can be the form of emulsion, emulsifiable paste, gel, spraying and mousse.The consumer of liking traditional conditioner composition is because conditioner can show higher conditioning characteristic, or because the consumption that can be easily changes conditioner according to the situation or the position of hair.And the conditioner of smooth and flexibility and good wet comb is liked providing to hair by consumer.
The usual method of giving the hair conditioning benefit is to use hair conditioner, as cationic surfactant and polymer, silicone conditioning agent, hydrocarbon and other organic oil and solid fat compounds of group such as aliphatic alcohol.Known cationic surfactant and polymer and oil and aliphatic compounds can increase the gloss of hair, give that it is moistening, softness and anlistatig effect, and still, they also make hair be clamminess or be greasy or the waxiness sense arranged.
Known have a high-molecular weight material, can provide the good conditioning characteristic as siloxane polymer, as smooth feeling and easy cardability.Do not think bound by theoryly, it is believed that because the low surface tension of siloxane polymer, siloxane polymer provides suitable conditioning effect to hair.But a large amount of silicone compounds causes exsiccant sensation or curling state.
The open S55-124711 of Japan Patent discloses a kind of hair composition that contains branched ester and water, described branched ester such as monostearate-pentaerythritol ester, tolyl silicone compounds, polyoxyethylene fatty acid ester.The open H5-124921 of Japan Patent discloses a kind of cosmetic composition that contains amphipathic compound, and described amphipathic compound has at least one long-chain branched alkyl or alkenyl and layered liquid crystal structure.The non-ionic amphiphilic chemical compound comprises the methyl branch fatty acid ester of tetramethylolmethane.
Therefore, need provide a kind of Wo 2008069000, it has improved conditioning effect such as slickness, flexibility and the wet easy cardability of sending out.
Among the present invention, developed a kind of Wo 2008069000 that comprises water-insoluble high molecular weight oily compound, it is in a liquid state and molecular weight is at least 800.The conditioning effect of this Wo 2008069000 improves, and improves as wettability, flexibility, free-flow, and viscosity reduces, and static is controlled, and can use with known conditioner.
The present invention relates to a kind of Wo 2008069000, comprising:
(a) oily compound of water-insoluble high molecular weight, its molecular weight is at least 800, and proportion is in a liquid state at 25 ℃ at least about 0.9, has following general formula (I):
A wherein
1, A
2, A
3And A
4Be C independently
1-C
30Alkyl, alkenyl, aryl, alkaryl, hydroxyalkyl, alkoxyl, alkoxyalkyl, acyl group, acyl alkyl and alkyl acyloxy, perhaps formula-(CH
2)
n-O-OCR, wherein R is C
1-C
30Side chain or the alkyl or the alkenyl of straight chain, n is the integer of 1-30;
(b) carrier.
This based composition satisfies the needs of Wo 2008069000, and it has improved conditioning effect, improves as wettability, flexibility, free-flow, and viscosity reduces, and static is controlled, and can use with known conditioner.
Detailed Description Of The Invention
Unless stated otherwise, all percents of the present invention all calculate with the weight of compositions, and all ratios all are weight ratios.Unless stated otherwise, all percent, ratio and relevant with the present invention become component all based on the actual amount of this composition, do not comprise that solvent, filler or other can be used as the raw material that is purchased the product blending constituent.
The present invention includes, be grouped into or mainly become to be grouped into by the composition of the following stated and any preferred or selectivity of the present invention by the one-tenth of the following stated.
All publications of the present invention, patent application and patent are all by document incorporated by reference.
Water-insoluble high molecular weight oily compound
Wo 2008069000 of the present invention comprises a kind of water-insoluble high molecular weight oily compound and carrier.Water-insoluble high molecular weight oily compound of the present invention is that those provide excellent conditioning performance such as slickness and easy cardability to hair.Be not wishing to be bound by theory, it is believed that water-insoluble oily chemical compound of the present invention can be deposited on the hair and conditioning hair.It is believed that this water-insoluble oily chemical compound covers hair surface, the result reduces the hair friction, provides slickness to hair.This insoluble high molecular weight oily compound is chemically stable under normal use and condition of storage.
Term used herein " insoluble oily chemical compound " means chemical compound at room temperature can not be fully soluble in water.When chemical compound with the concentration more than 1.0%, when more preferably mixing with water with the concentration more than 0.5%, chemical compound is separated into biphase from water to form unsettled colloid in water temporary transient the dispersion then in a short time.
The molecular weight of the water-insoluble oily chemical compound that the present invention is used,,, is in a liquid state under 25 ℃ as long as the proportion of chemical compound is 0.9 at least more preferably at least about 1200 preferably at least about 1000 at least about 800.
The used water-insoluble oily chemical compound of the present invention comprises those chemical compounds of following formula (I):
A wherein
1, A
2, A
3And A
4Be C independently
1-C
30Alkyl, alkenyl, aryl, alkaryl, hydroxyalkyl, alkoxyl, alkoxyalkyl, acyl group, acyl alkyl and alkyl acyloxy, perhaps formula-(CH
2)
n-O-OCR, wherein R is C
1-C
30Side chain or the alkyl or the alkenyl of straight chain, n is the integer of 1-30, preferably equals 1;
Preferably, the oily compound of water-insoluble high molecular weight of the present invention is an ester, wherein A
1, A
2, A
3And A
4Be ester group, perhaps A
1, A
2, A
3And A
4In three be ester group, another is an alkyl.More preferably, the oily compound of water-insoluble high molecular weight of the present invention is C
12-C
22Fatty acid and the ester of tetramethylolmethane, C
12-C
22Fatty acid and the ester of trimethylol-alkanes, and composition thereof.
The oily compound of preferred water-insoluble high molecular weight is those A
1, A
2, A
3And A
4Have identical substituent group, and these substituent groups are chemical compounds of ester group.
The oily compound of the preferred water-insoluble high molecular weight of the present invention is four isostearic acid pentaerythritol esters, three isostearic acid trimethylolpropane base esters, four pentaerythritol oleates, three oleic acid trihydroxymethylpropanyl esters and composition thereof.
Suitable ester compounds comprises, as four isostearic acid pentaerythritol esters and three oleic acid trihydroxymethylpropanyl esters (they can have been bought with trade name KAKPTI and KAKTTI from Kokyo Alcohol), and four pentaerythritol oleates and three oleic acid trihydroxymethylpropanyl esters (they can have been bought with trade name PTO and ENUJERUBU TP3SO respectively from Shinnihon Rika).
The consumption of the oily compound of water-insoluble high molecular weight is about 0.1-20.0% of composition weight, preferably about 0.1-10.0%, more preferably from about 0.2-5.0%.
Carrier
Wo 2008069000 of the present invention contains a kind of carrier.According to selecting the consumption and the kind of carrier with the desirable characteristics of the compatibility of other component and product.
The used carrier of the present invention comprises water, lower alkyl alcohol, polyhydric alcohol and composition thereof.The used lower alkyl alcohol of the present invention is C
1-C
6Alkyl monocarbon alcohol, preferably C
2-C
3Alkylol.Preferred lower alkyl alcohol is ethanol, isopropyl alcohol and composition thereof.Polyhydric alcohol used herein comprises, as propylene glycol, hexylene glycol, glycerol and propylene glycol, and composition thereof.
Non-volatile water-insoluble low-molecular-weight oily compound
Hair care composition of the present invention can further contain non-volatile water-insoluble low-molecular-weight oily compound.Non-volatile water-insoluble low-molecular-weight oily compound of the present invention is those chemical compounds that conditioning performance of excellence is provided to hair.Do not think bound by theoryly, it is believed that non-volatile water-insoluble low-molecular-weight oily compound can easily be penetrated in the hair, the result be flexibility to hair is provided and increase head and a compliance.
Term used herein " fixedness " means water-insoluble low-molecular-weight oily compound and shows very low or do not have tangible vapour pressure in environmental condition (as 1 atmospheric pressure, 25 ℃).
The molecular weight of the non-volatile water-insoluble low-molecular-weight oily compound that the present invention is used is at least about 800, preferably less than about 500, is more preferably less than approximately 300, as long as the proportion of chemical compound is at least about being 0.8, and is in a liquid state at 25 ℃.
Preferably, the used non-volatile water-insoluble low-molecular-weight oily compound of the present invention is selected from fatty acid, derivative of fatty acid of the hydrocarbon of 10-40 carbon atom, the aliphatic alcohol of about 10-30 carbon atom, about 10-30 carbon atom and composition thereof.
Useful hydrocarbon comprises straight chain, ring-type and branched-chain hydrocarbons, and it can be saturated or unsaturated.Suitable hydrocarbon with 10-40 carbon atom comprises, as isoparaffin and mineral oil.These hydrocarbon can be from having bought with trade name Isopar as Exxon Co., and bought with trade name Benol from Witco Corp..
The used aliphatic alcohol of the present invention comprises those about 10-30 carbon atoms, preferably 12-22 carbon atom, the alcohol of 16-22 carbon atom more preferably from about.These aliphatic alcohol can straight chain or the alcohol of straight chain, can be saturated or unsaturated alcohol, preferred unsaturated alcohol.Suitable aliphatic alcohol comprises, as oleyl alcohol, isooctadecanol, tridecyl alcohol, decyl tetradecanol and octyldodecanol.These alcohol can be from having bought as Shinnihon Rika.
The used fatty acid of the present invention comprises that those contain 10-30 the carbon atom of having an appointment, preferably about 12-22 carbon atom, the acid of more preferably about 16-22 carbon atom.These fatty acids can be straight or brancheds, can be saturated or unsaturated.Suitable fatty acids comprises, as oleic acid, linoleic acid, isostearic acid, linolenic acid and ethyl linolenic acid.
Derivative of fatty acid that the present invention limited and fatty alcohol derivative comprise ester as aliphatic alcohol, alkoxy fatty alcohols, the Arrcostab of aliphatic alcohol, Arrcostab of alkoxy fatty alcohols and composition thereof.The limiting examples of derivative of fatty acid and fatty alcohol derivative comprises, as methyl linoleate, Ethyl linoleate, linoleic acid isopropyl ester, Ceraphyl 140A, acid isopropyl, ethyl oleate, oleic acid octyl group dodecyl ester, oleic acid oleic alcohol ester, decyl oleate, butyl oleate, methyl oleate, stearic acid octyl group dodecyl ester, isostearic acid octyl group dodecyl ester, different palmitic acid octyl group dodecane ester, different octyl pelargonate, octyl pelargonate, the own ester of isostearic acid, isostearic acid isopropyl ester, different isodecyl pelargonate and Oleth-2 (oil base polyoxyethylene ether).
Extremely preferred non-volatile water-insoluble low-molecular-weight oily compound is selected from isostearic acid octyl group dodecane ester, methyl myristate, oleyl alcohol, has the hydrocarbon of about 14-40 carbon atom, and composition thereof.
The limiting examples of above-claimed cpd is at International Cosmetic IngredientDictionary (international cosmetic composition dictionary), the 5th edition, 1993 and CTFA CosmeticIngredient Handbook (CTFA cosmetic composition handbook), second edition, 1992 find, it is introduced the present invention as a reference in full.
The content of non-volatile low molecular weight oily compound is about the 0.1-10.0% of composition weight, preferably about 0.2-5.0%, more preferably from about 0.2-2.0%.
The insoluble fatty compound of solid water
Hair care composition of the present invention can further contain the insoluble fatty compound of solid water.Without being limited by theory, it is believed that the insoluble fatty compound of solid water of the present invention can cover hair surface, and make hair smooth, and make hair be easy to combing by reducing coefficient of friction.
Term used herein " solid water is insoluble " fatty compound means that chemical compound can not be fully soluble in water under the room temperature.When chemical compound be higher than 1.0% concentration, preferably when being higher than 0.5% concentration and mixing with water, chemical compound remains on initial state, and does not dissolve.Term " solid " means chemical compound and has crushing resistance, is not easy to change shape, is different from glue, cream, the liquid state under 25 ℃ or gaseous state.
The used insoluble fatty compound of solid water of the present invention comprise those be selected from the hydrocarbon that has about 20 carbon atoms at least, at least about the saturated fatty alcohol of 14 carbon atoms, fatty acid, derivative of fatty acid, fatty alcohol derivative, steroid and composition thereof at least about 10 carbon atoms.Because its different characteristic, the insoluble fatty compound of solid water (as hydrocarbon, saturated fatty alcohol, fatty acid, derivative of fatty acid or fatty alcohol derivative) are different from the chemical compound that " non-volatile water-insoluble low-molecular-weight oily compound " part is exemplified.
It should be understood that in these chemical compounds some has the character of non-ionic surface active agent, can classify as non-ionic surface active agent.But given classification do not want being limited to this concrete chemical compound, but so does so that classify and name.
The used saturated fatty alcohol of the present invention has about 14 carbon atoms at least, preferably at least about 14-22 carbon atom.These saturated aliphatic alcohol can be the alcohol of straight or branched.Suitable saturated fatty alcohol comprises, as spermol, stearyl alcohol and tadenan.These aliphatic alcohol can be from ShinnihonRika for example with trade name Konol series, or bought with trade name NAA series from Nippon Oil.
The used fatty acid of the present invention has about 10 carbon atoms at least.These fatty acids can be the acid of straight or branched, can be saturated or undersaturated.The present invention also comprises binary acid, ternary acid and other polyprotic acid that satisfies carbon atom required for the present invention.Suitable fatty acids comprises, as stearic acid, behenic acid, Palmic acid, arachidonic acid and decanedioic acid.These fatty acids can be from having bought with trade name Noe-Fat as Akzo, from having bought with trade name Hystrene as Witco Corp., or bought with trade name derma from Vevy.
Derivative of fatty acid that the present invention limited and fatty alcohol derivative comprise the ester of fatty acid, as the aliphatic alcohol ester of acid and the alcohol ester of the ethoxylation of acid.The limiting examples of derivative of fatty acid and fatty alcohol derivative comprises, as glyceryl monostearate, geoceric acid stearyl alcohol ester, ethyl stearte, stearic acid cetyl, cetin and myristyl myristate.
Suitable steroid comprises, as cholesterol, has bought with trade name Nikkol AguasomeLA from Nikko.
The extremely preferred insoluble aliphatic compounds of solid water are the saturated fatty alcohols with about 14-22 carbon atom.
The limiting examples of above-claimed cpd is at International Cosmetic IngredientDictionary (international cosmetic composition dictionary), the 5th edition, 1993 and CTFA CosmeticIngredient Handbook (CTFA cosmetic composition handbook), second edition, 1992, it is introduced the present invention as a reference in full.
The content of the insoluble fat of solid water family compound is the 0.1-20% of compositions approximately, preferably about 1-15%, more preferably from about 4-10%.
Additional conditioner
In addition, the present invention can comprise known other conditioner in the industry.Suitable conditioner comprises cationic surfactant, cationic polymer, silicone compounds and its mixture.The content of these conditioners in care composition of the present invention is about 0.01% to about 20%.
Cationic surfactant
Hair conditioner of the present invention can contain one or more cationic surfactants in addition as conditioner.
The used cationic surfactant of the present invention is well known to a person skilled in the art.
Be used for cationic surfactant of the present invention for having those cationic surfactants of following general formula (I):
Wherein, R
1, R
2, R
3And R
4In at least one aryl, alkoxyl, polyoxyalkylene, alkyl amido, hydroxyalkyl, aryl or alkaryl that is independently selected from aliphatic group or has about at the most 22 carbon atoms with 8-30 carbon atom, R
1, R
2, R
3And R
4In remaining is independently selected from aliphatic group with about 22 carbon atoms of 1-or aryl, alkoxyl, polyoxyalkylene, alkyl amido, hydroxyalkyl, aryl or the alkaryl with about at the most 22 carbon atoms; X is for becoming salt anionic, as halogen ion (as chloride ion, bromide ion), acetate, citrate, lactate, glycolic acid ester group, phosphate radical, nitrate anion, sulfonate radical, sulfate radical, alkyl sulfate and alkyl azochlorosulfonate.Aliphatic group de-carbon and hydrogen atom also can comprise ehter bond and other group such as amino outward.The long-chain aliphatic group group of 12 carbon atoms or more a plurality of carbon atoms according to appointment can be saturated group or unsaturated group.Preferred R
1, R
2, R
3And R
4Be independently selected from C
1-C
22Alkyl.The non-limiting example that is used for cationic surfactant of the present invention comprises the material with following CTFA name: quaternium-8, quaternium-24, quaternium-26, quaternium-27, quaternium-30, quaternium-33, quaternium-43, quaternium-52, quaternium-53, quaternium-56, quaternium-60, quaternium-62, quaternium-70, quaternium-72, quaternium-75, quaternium-77, quaternium-78, quaternium-80, quaternium-81, quaternium-82, quaternium-83, quaternium-84 and its mixture.
Also preferred cationic surfactants is the cationic surfactant of hydrophilic replacement, and wherein, one of substituent group comprises one or more aromatics, ether, ester, acylamino-or amino part at least, and its substituent group or key as basic chain exists, wherein, and R
1-R
4In the group at least one comprises one or more hydrophilic segments, and this hydrophilic segment is selected from alkoxyl (preferred C
1-C
3Alkoxyl), polyoxyalkylene (preferred C
1-C
3Polyoxyalkylene), alkyl amido, hydroxyalkyl, Arrcostab and its mixture.The cationic conditioning surfactant of preferred hydrophilic replacement comprises about 10 the nonionic hydrophilic segments within above-mentioned scope of 2-.The cationic surfactant of preferred hydrophilic replacement comprises the surfactant of following formula (II)-Shi (VII):
Wherein, n is 8-28, and x+y is that 2-is about 40, Z
1Be short-chain alkyl, preferred C
1-C
3Alkyl, more preferably methyl, or (CH
2CH
2O)
zH, wherein, x+y+z is at most 60, and X is for becoming salt anionic as defined above:
Wherein, m is 1-5, R
5, R
6And R
7In one or more be C independently
1-C
30Alkyl; All the other are CH
2CH
2OH, R
8And R
9And R
10In one or both be C independently
1-C
30Alkyl, all the other are CH
2CH
2OH, X is for becoming salt anionic as defined above;
Wherein, Z
2Be alkyl, preferred C
1-C
3Alkyl, more preferably methyl; Z
3Be the short chain hydroxyalkyl, preferred methylol or ethoxy; P and q are the integer of 2-4 (comprising 2,4) independently, preferred 2-3, more preferably 2; R
11And R
12Independently for replacing or unsubstituted alkyl preferred C
12-C
20Alkyl or alkenyl, X are aforesaid one-tenth salt anionic;
Wherein, R
13Be alkyl, preferred C
1-C
3Alkyl, more preferably methyl; Z
4And Z
5Be short-chain hydrocarbon group independently, preferred C
2-C
4Alkyl or alkenyl, more preferably ethyl; A is that 2-is about 40, and preferably about 7-is about 30, and X is aforesaid one-tenth salt anionic;
Wherein, R
14And R
15Be C independently
1-C
3Alkyl, preferable methyl; Z
6Be C
12-C
22Alkyl, alkyl carboxyl or alkyl amido; A is a protein, preferred collagen protein, keratin, lactoprotein, fibroin, soybean protein, wheat protein or its hydrolysed form; X is aforesaid one-tenth salt anionic;
Wherein, b is 2 or 3, R
16And R
17Be C independently
1-C
3Alkyl, preferable methyl; X is aforesaid one-tenth salt anionic.The non-limiting example that is used for the cationic surfactant of hydrophilic replacement of the present invention comprises the material with following CTFA name: quaternium-16, quaternium-61, quaternium-71, quaternium-79 hydrolytic collagen, quaternium-79 hydrolysis of keratin, quaternium-79 lactoalbumin hydrolysate, quaternium-79 hydrolyzed silk protein, quaternium-79 hydrolyzed soybean protein, quaternium-79 hydrolyzed wheat protein.Particularly preferred chemical compound comprises the following material that is purchased: VARIQUATK1215 and 638 (available from Witco Chemical); MACKPRO KLP, MACKPRO WLW, MACKPRO MLP, MACKPRO NSP, MACKPRO NLW, MACKPRO WWP, MACKPRO NLP, MACKPRO SLP (available from Mclntyre); ETHOQUAD 18/25, ETHOQUAD O/12PG, ETHOQUAD C/25, ETHOQUADS/25 and ETHODUOQUAD (available from Akzo); DEHYQUAT SP (available from Henkel) and ATLAS G265 (available from ICI Americas).
The primary, the salt of the second month in a season and uncle's fatty amine is also suitable to cationic surfactant.The alkyl group of this amine preferably has about 22 carbon atoms of about 12-, and it can be and replaces or substituted radical not.Particularly suitable be the fat tertiary amine that acylamino-replaces.Be used for this amine of the present invention and comprise the amino propyl-dimethyl amine of stearoyl, the amino propyl group diethylamide of stearoyl, the amino ethyl diethylamide of stearoyl, the amino ethyl dimethyl amine of stearoyl, palmityl aminopropyl dimethyl amine, palmityl aminopropyl diethylamide, palmityl amino-ethyl diethylamide, palmityl amino-ethyl dimethyl amine, docosyl acylamino-propyl-dimethyl amine, docosyl acylamino-propyl group diethylamide, docosyl acylamino-ethyl diethylamide, docosyl acylamino-ethyl dimethyl amine, eicosyl acylamino-propyl-dimethyl amine, eicosyl acylamino-propyl group diethylamide, eicosyl acylamino-ethyl diethylamide, eicosyl acylamino-ethyl dimethyl amine, diethylamino ethyl stearmide.Useful dimethyl stearylamine, dimethyl Semen sojae atricolor amine (soyamine), Semen sojae atricolor amine, Semen Myristicae amine, tridecyl amine, ethyl stearic amine, N-tallow propane diamine, ethoxylation (having 5 mole ethylene oxides) stearylamine, dihydroxy ethyl stearic amine and eicosyl docosyl amine in addition.These amine also can be used in combination with acid, described acid such as L-glutamic acid, lactic acid, hydrochloric acid, malic acid, succinic acid, acetic acid, fumaric acid, tartaric acid, citric acid, L-glutamic acid hydrochloride and composition thereof, more preferably L-glutamic acid, lactic acid and citric acid.Cationic amine surfactant of the present invention is disclosed in USP 4,275,055 (being issued to Nachtigal etc. on June 23rd, 1981) described those, the document is incorporated herein by reference.
Be used for cationic surfactant of the present invention and also can comprise a plurality of quaternary ammonium parts or amino part, or its mixture.
Being used for cationic surfactant of the present invention can be used as emulsifying agent and is used for this compositions.
Cationic polymer
Wo 2008069000 of the present invention can further comprise one or more cationic polymers as conditioner.Term " polymer " used in the present invention " comprise raw material through a kind of monomer polymerization or two kinds (they being copolymer) or multiple monomer polymerization.
Preferably, cationic polymer is a water-soluble cationic polymer." water solublity " cationic polymer refers to such polymer: it fully is dissolved in the water with 0.1% concentration in 25 ℃ of water (distilled water or quite thing) and forms naked eyes and see limpid basically solution.Preferably, this polymer fully dissolves the limpid substantially solution of formation with 0.5% concentration, more preferably is to form limpid substantially solution with 1.0% concentration.
Cationic polymer of the present invention weight average molecular weight generally be at least about 5000, normally at least about 10000, less than about 1,000 ten thousand.Preferably, molecular weight from about 100000 to about 200 ten thousand.Cationic polymer has for example part of quaternary ammonium or cation amino part and composition thereof of cation nitrogen moiety usually.
Cationic charge density is preferably at least about 0.1meq/g, more preferably at least about 1.5meq/g, more preferably at least about 1.1meq/g, further preferably at least about 1.2meq/g.The cationic charge density of this cationic polymer is determined according to the Kjeldahl method.Those skilled in the art know that the charge density of amido polymer can change according to the isoelectric point, IP of pH value and amino group.Charge density should be in the above range under the pH that expection is used.
For cationic polymer, can use anionic counter-ion, as long as can satisfy the water solublity standard.Suitable counter ion counterionsl gegenions comprise halogen (for example, Cl, Br, I or F, preferred Cl, Br or I), sulfate radical and methyl ester sulfate radical.Can also use other ion, because above-mentioned ion right and wrong are exclusive.
The cation nitrogen moiety exists as the substituent group on total monomeric unit part partly of cationic hair conditioning polymer usually.Therefore, cationic polymer comprises that monomeric unit and other the present invention that quaternary ammonium or cationic amine replace are called the unitary copolymer of the unitary non-cationic of spacer monomers, ter-polymers etc.These polymer are known in the present technique field, and their kind is referring to CTFA cosmetic composition handbook, and the 3rd edition (by Estrin, Crosley and Haynes edit, The CosmeticToiletry and Fragrance Association, Inc., Washington, D.C., 1982).
Suitable cationic polymers for example comprises vinyl monomer and the water solublity basic monomer in interval such as acrylamide, MAAm, alkyl and dialkyl group acrylamide, alkyl and dialkyl group MAAm, alkyl acrylate, methacrylate Arrcostab, vinyl caprolactone and the vinylpyrrolidone copolymers with cationic amine or quaternary ammonium functional group.The monomer that alkyl and dialkyl group replace preferably has C
1-C
7Alkyl group more preferably is C
1-C
3Alkyl group.Other suitable interval base monomer comprises vinyl esters, vinyl alcohol (being produced by the polyvinyl acetate hydrolysis), maleic anhydride, propylene glycol and ethylene glycol.
According to the concrete kind and the pH value of compositions, cationic amine can be primary, the second month in a season or tertiary amine.Generally, the preferred second month in a season and tertiary amine are especially weighed amine.
The vinyl monomer that amine replaces can amine the form polymerization, optionally be converted into ammonium salt by quaterisation then.Amine also can carry out similarly quaternized after forming polymer.For example, by with the reaction of the salt of sub-RX, tertiary amine functional group can be by quaternized, wherein R is a short-chain alkyl, preferred C
1-C
7Alkyl, more preferably C
1-C
3Alkyl, X are the aniones that forms water soluble salt with this quaternised ammonium salt.
Suitable cation amino and quaternary ammonium monomer for example comprise the vinyl compound that replaces with following compounds: propenoic acid dialkyl aminoalkyl ester, the methacrylate dialkyl aminoalkyl ester, acrylic acid alkyl monosubstituted amino Arrcostab, methacrylate alkyl monosubstituted amino Arrcostab, trialkyl isobutene. acyl-oxygen base alkylammonium salt, trialkyl acryloxyalkyl ammonium salt, the diallyl quaternary ammonium salt, and have the ring-type cation and contain azo-cycle such as pyridiniujm, the vinyl quaternary ammonium monomer of imidazole salts and quaternized ketopyrrolidine, for example alkyl vinyl imidazole salts, alkylvinylpyridines salt, alkyl vinyl ketopyrrolidine salt.These monomeric moieties are low alkyl group, for example C preferably
1-C
3Alkyl, more preferably C
1And C
2Alkyl.Be used for the vinyl monomer that suitable amine of the present invention replaces and comprise propenoic acid dialkyl aminoalkyl ester, methacrylate dialkyl aminoalkyl ester, dialkyl aminoalkyl acrylamide and dialkyl aminoalkyl MAAm, wherein alkyl is preferably C
1-C
7Alkyl more preferably is C
1-C
3Alkyl.
Cationic polymer of the present invention comprises the mixture by the monomer of amine and/or quaternary ammonium-substituted and/or the compatible deutero-monomeric unit of spacer monomers.
Suitable cationic hair conditioning polymer comprises, for example: the copolymer of l-vinyl-2-pyrrolidone and 1-vinyl-3-methylimidazole salt (for example villaumite) is (in the industry by Cosmetic, Toiletry, and Fragrance Association, " CTFA " is called Polyquaternium-16), for example by the (Parsippany of BASFWyandotte company, NJ, the product (for example, LUVIQUAT FC370) of the commodity that USA) are purchased LUVIQUAT by name; The copolymer (being called Polyquaternium-11 by CTFA in the industry) of l-vinyl-2-pyrrolidone and methacrylate dimethyl aminoethyl ester, for example by the (Wayne of Gaf company, NJ, those products of the commodity that USA) are purchased GAFQUAT by name are (for example, GAFQUAT755N); The polymer of cation diallyl quaternary ammonium, for example comprise, the copolymer of the homopolymer of dimethyl diallyl ammonium chloride and acrylamide and dimethyl diallyl ammonium chloride, (CTFA) is called as Polyquaternium 6 and Polyquaternium 7 respectively in industry; With the salt of the mineral acid of the aminoalkyl ester of the homopolymer of unsaturated carboxylic acid and copolymer, referring to USP4009256 (being incorporated herein by reference) with 3 to 5 carbon atoms.
Other operable cationic polymer comprises polysaccharide polymer, for example cationic cellulose derivative and cationic starch derivative.
Be applicable to that cationic polysaccharide polymer raw material of the present invention comprises the material of following formula:
Wherein A is an anhydroglucose residue group, for example starch or cellulose anhydroglucose residue; R is alkylidene oxyalkylene, polyoxy alkylidene or hydroxy alkylidene or its mixed group; R
1, R
2And R
3Be alkyl, aryl, alkaryl, aralkyl, alkoxyalkyl or alkoxy aromatic yl group independently, each group contains about 18 carbon atoms of as many as, and the sum of the carbon atom of each cationic moiety (is R
1, R
2And R
3In the sum of carbon atom) preferably be about 20 or still less, X is foregoing anionic counter-ion.
Cationic cellulose can (Edison, NJ be USA) with JR from Amerchol company
And LR
The equal proportion polymer obtain, they are as the epoxide reactive salt that hydroxyethyl-cellulose and trimethyl ammonium replace, (CTFA) is called Polyquaternium 10 in industry.Another kind of cationic cellulose comprises the polymer quaternary ammonium salt of the epoxide reactive hydroxyethyl-cellulose that replaces with the lauryl dimethyl ammonium, and (CTFA) is called as Polyquaternium 24 in industry.These raw materials can (Edison, NJ be USA) with trade name Polymer LM-200 from Amerchol company
Obtain.
Other operable cationic polymer comprises the cationic guar gum derivant, for example hydroxypropyl-trimethyl ammonium chloride guar gum (can be purchased with its Jaguar R series of products from Celanese company).Other material comprises the cellulose of the cellulose ether that contains quaternary nitrogen (for example, being documented among the USP 3962418 as cited literature 2) and etherificate and the copolymer of starch (for example, being documented among the USP3958581 as cited literature 2).
Silicone compounds
Other used conditioner of the present invention comprises silicone compounds.Wo 2008069000 of the present invention can comprise solvable or soluble or the solvable or insoluble silicone conditioning agent of fixedness of volatility." soluble " means silicone conditioning agent can be miscible to form a mutually in-phase part with the carrier of compositions." insoluble " means that siloxanes formation separates with carrier, mutually discontinuous, as is the form of the suspension of silicone emulsion or droplets of siloxane.
The used dispersive siloxanes of fixedness of the present invention is preferably about 1 25 ℃ of viscosity that have, 000-2, and 000,000 centistoke, more preferably about 10,000-1,800,000 centistokes most preferably are 100,000-1,500,000 centistokes.Viscosity can be measured by glass capillary tube viscometer, and as Dow CorningCorporate Test Method CTM004, on July 20th, 1970 is described, and it is introduced the present invention as a reference in full.Suitable siloxanes fluids comprises poly-alkylsiloxane, poly-aryl siloxanes, poly-alkaryl siloxanes, polyether siloxane copolymer and composition thereof.Also can use other to have the fixedness silicone compounds of hair conditioning performance.
The dispersive silicone compounds of fixedness of the present invention also comprises poly-alkyl or the poly-aryl siloxanes with following formula (I):
Wherein R is an alkyl or aryl, and x is about 7 to about 8000 integer.The group of " A " expression sealing siloxane chain end.The alkyl or aryl (A) that replaces in the alkyl or aryl (R) or the siloxane chain end of siloxanes chain substitution can be an any structure, as long as the siloxanes of gained at room temperature keeps fluid, can disperse, non-stimulated, avirulence, harmless when being used for hair, can be compatible with other composition in the compositions, under the use of routine and condition of storage is chemically stable, and can be deposited on the hair and to hair has opsonic action.The proper A group comprises hydroxyl, methyl, methoxyl group, ethyoxyl, propoxyl group and aryloxy group.Two R groups on silicon atom can be identical or different groups.Preferred two R groups are represented identical group.The suitable R group comprises methyl, ethyl, propyl group, phenyl, aminomethyl phenyl and phenyl methyl.Preferred siloxane polymer is polydimethylsiloxane, poly-di-ethyl siloxane, PSI.Particularly preferably be known polydimethylsiloxane as dimethicone.Operable poly-alkylsiloxane comprises as polydimethylsiloxane.These siloxanes can from as General Electric Company with its ViscasilR and SF 96 series, and bought with Dow Corning 200 series from DowCorning.
Also can use polyoxyethylene alkyl aryl radical siloxane fluid, comprise as PSI.These siloxanes can from as General Electric Company with its SF 1075 serial aminomethyl phenyl fluids, or bought with 556 Cosmetic Grade Fluid from Dow Corning.
For improving the gloss of hair, the present invention especially preferably uses the siloxanes of Gao Fanghua, for example have refraction index be about 1.46 or bigger, especially be about 1.52 or the poly-ethylsiloxane of bigger high benzeneization.When using the silicone compounds of these high refractive indexes, they should mix to reduce surface tension and to improve its film forming ability as surfactant or silicone resin with spreading agent (spreading agent) as described below.
Operable non-volatile dispersive silicone compounds comprises the polydimethylsiloxane as the poly(propylene oxide) modification, although can use the mixture of oxirane or oxirane and expoxy propane.The content of oxirane and poly(propylene oxide) should be enough low so that can not disturb the dispersibility of siloxanes.These materials also are known as dimethicone copolyol.
Other nonvolatile dispersive silicone compounds comprises the amino material that replaces.The silicone compounds that suitable alkylamino replaces comprises the chemical compound of following structure (II):
Wherein R is CH
3Or OH, x and y are the integers that depends on the desired molecule amount, mean molecule quantity is approximately 5000-10000.This polymer is also referred to as amination polydimethylsiloxane (amodimethicone).
The siloxanes that suitable amino replaces comprises those chemical compounds with formula (III) expression
(R
1)
aG
3-a-Si-(OSiG
2)
n-(OSiG
b(R
1)
2-b)
m-O-SiG
3-a(R
1)
a(III) wherein G is selected from hydrogen, phenyl, OH, C
1-C
8Alkyl, preferable methyl; A represents 0 or 1 to 3 integer, preferably equals 0; B represents 0 or 1, preferably equals 1; N+m's and be 1 to 2000 numeral, preferred 50 to 150, n represents 0 to 1999 numeral, and is preferred 49 to 149, m represents an integer of 1 to 2000, preferred 1 to 10; R
1Be formula C
qH
2qThe unit price residue of L, wherein q is 2 to 8 integer, L is selected from following group:
-N(R
2)CH
2-CH
2-N(R
2)
2
-N(R
2)
2
-N(R
2)
3A
-
-N (R
2) CH
2-CH
2-NR
2H
2A
-R wherein
2Be selected from hydrogen, phenyl, benzyl, saturated hydrocarbon residue, preferably contain the alkyl residue of 1 to 20 carbon atom, A
-The expression halide ion.
The particularly preferred amino siloxanes that replaces corresponding to formula (III) is the polymer that is known as " trimethyl silyl amination polydimethylsiloxane (trimethylsilylamodimethicone) " of formula (IV):
N and m select according to the definite molecular weight of required compound in this structural formula.The siloxanes that other amino that can use replaces is represented with formula V:
R wherein
3Expression has the univalence hydrocarbyl of 1 to 18 carbon atom, preferred alkyl or alkenyl such as methyl; R
4Expression alkyl, preferably C
1-C
18Alkylidene or C
1-C
18, C more preferably
1-C
8Alkylidene oxygen residue; Q
-Be halide ion, preferred chlorine; R represents 2 to 20 average statistics value, preferred 2 to 8; S represents 20 to 200 average statistics value, preferred 20 to 50.The preferred polymer of this class can have been bought with trade name " UCAR SILICONE ALE 56 " from UnionCarbide.
The reference material that discloses suitable nonvolatile dispersive silicone compounds comprises USP2,826,551 (Geen); USP3,963,500 (authorizing Drakoff on July 22nd, 1976); USP4,364,837 (Pader); British patent 849,433 (Woolston); These full patent texts are drawn be reference.Introduce in full the present invention as a reference also have by Patrarch Systems Inc., " the Silicon Compounds " of 1984 classification.This list of references provides widely (although not being exhaustive) suitable silicone compounds series.
The another kind of nonvolatile dispersive siloxanes that is particularly useful is a siloxane glue material.Term used herein " siloxane glue material " refers to 25 ℃ of following viscosity more than or equal to 1,000, the polysiloxane material of 000 centistoke.Will be appreciated that siloxane glue material described in the invention can overlap with the disclosed silicone compounds in front.Do not want this overlapping as any restriction in these materials.Siloxane glue material is described by Petrach, other comprise USP 4,152,416 (authorizing people such as Spitzer on May 1st, 1979) and Noll, Walter, Chemistry and Technology of Silicones, New York:Academic Press 1968.General ElectricSilicone Rubber Product Data Sheets SE30, SE33, SE54 and the SE76 in addition of siloxane glue material are described.The list of references of all these descriptions drawn in full be reference.It is about 200,000 that the weight average molecular weight of " siloxane glue material " usually surpasses, about usually 200,000-1,000,000.Instantiation comprises polydimethylsiloxane, poly-(dimethyl siloxane ethylene methacrylic radical siloxane) copolymer, poly-(dimethyl siloxane diphenyl siloxane ethylene methacrylic radical siloxane) copolymer and composition thereof.
Also can adopt silicone resin, it is highly cross-linked polymer siloxane system.In the silicone resin production process, make trifunctional with and four senses close silane and mix in simple function or two senses or simple function and two functional silanes and introduce crosslinked.Just as known in the art, can change according to the specific silane unit that mixes in the silicone resin for forming the required degree of cross linking of silicone resin.Usually, think and have abundant trifunctional and four-functional group siloxanyl monomers unit that (thereby crosslinked fully) is so that their dryings can become the silicone material of rigidity or hard film is silicone resin.The ratio of oxygen atom and silicon atom shows the crosslinked level in concrete silicone material.It will be silicone resin of the present invention usually that the ratio of oxygen atom and silicon atom is at least about 1.1 silicone material.The preferred oxygen atom was at least about 1.2: 1.0 with the ratio of silicon atom.The silane that is used to produce silicone resin comprises monomethyl, dimethyl, trimethyl, a phenyl, diphenyl, aminomethyl phenyl, a vinyl and methyl ethylene chlorosilane, and tetrachloro silicane, and the most normal employing is methyl substituted silane.Preferred resin is provided with GE SS4230 and SS4267 by General Electric.Usually evaporable or nonvolatile siloxanes fluids provides commercially available silicone resin with low viscosity with dissolved form.Should supply the present invention used silicone resin with this dissolved form, and it is added in the compositions of the present invention, this be conspicuous for those of ordinary skills.Although be not subjected to the restriction of any theory, it is believed that silicone resin can increase other silicone compounds on hair deposition and can improve the gloss of hair because of its high refractive index.
Other useful silicone resin is the silicone resin powder, and as by CTFA nomenclature called after polymethylsilsequioxane, it can be from Toshiba Silicones with Tospearl
TMBought.
The background material of relevant silicone compounds, the production method that comprises content that siloxanes fluids, siloxane glue and silicone resin are discussed and silicone compounds can be referring to " polymer science and engineering encyclopedia (Encyclopedia of Polymer Science and Engineering) ", the 15th volume, second edition, the 204-308 page or leaf, John Wiley ﹠amp; Sons.Inc., 1989 ", the document is incorporated herein by reference.
Silicone material and silicone resin can be easily according to well known to a person skilled in the art i.e. " MDTQ " nomenclature identification of shorthand nomenclature system.In this system, siloxanes is that the various monomeric units according to the existence of forming siloxanes are described.In brief, symbol M is represented simple function unit (CH
3)
3SiO
0.5D represents two functional unit (CH
3)
2SiO; T represents trifunctional units (CH
3) SiO
1.5Q represents four functional unit SiO
2Unit symbol apostrophe such as M ', D ', T ', the substituent group of Q ' representative except that methyl, all need concrete definition at every turn.Typical replaceable substituent group is vinyl, phenyl, amino, hydroxyl etc.In the MDTQ system, various unitary mol ratios, perhaps the subscript with symbol indicates every kind of unitary total number (or its meansigma methods) in the siloxanes, perhaps with concrete indicated ratio and binding molecule amount, finishes the description to silicone material.In silicone resin, T, Q, T ' and/or Q ' compare with D, D ', M and/or M ' has relative high mole, then shows the crosslinking degree height.But as preceding discussion, crosslinked aggregate level also can be represented by the ratio of oxygen and silicon.
The preferred MQ of silicone resin of the present invention, MT, MTQ, MDT and MDTQ resin.Thereby preferred siloxanes substituent group is a methyl.Preferred especially MQ resin, wherein M: Q ratio is about 0.5: 1.0-1.5: 1.0, and the mean molecule quantity of resin is about 1000-10000.
Additional surfactant
Wo 2008069000 of the present invention can also comprise additional surfactant.These additional surfactant comprise amphoteric surfactant, zwitterionic surfactant, non-ionic surface active agent, anion surfactant and their mixture that does not influence care composition of the present invention.
Additional surfactants is particularly useful to the spraying or the compositions of mousse form, and wherein additional surfactants be used for suspending conditioner and other is insoluble to the component of carrier.Generally, the amount of additional surfactants is about 0.1% to about 15%, preferred about 0.3% to about 10% of a composition weight.According to amount and the kind of selecting additional surfactants with the compatibility and the desirable product feature of other component.
Amphoteric surfactant and zwitterionic surfactant
Compositions of the present invention can comprise amphoteric surfactant and/or zwitterionic surfactant.
Be used for amphoteric surfactant of the present invention and comprise aliphatic secondary amine and tertiary amines derived thing, wherein aliphatic group can be the straight or branched group, and, one of aliphatic series substituent group comprises about 18 carbon atoms of about 8-, and another comprises a kind of anionic water solubilizing group such as carboxyl, sulfonate radical, sulfate radical, phosphate radical or phosphonate radical.
Be used for zwitterionic surfactant of the present invention and comprise aliphatic quaternary ammonium, Phosphonium and sulfonium compound, wherein aliphatic group is the straight or branched group, and, one of aliphatic series substituent group comprises about 8-18 carbon atom, and another comprises a kind of anionic group such as carboxyl, sulfonate radical, sulfate radical, phosphate radical or phosphonate radical.The general formula of these chemical compounds is as follows:
Wherein, R
2Comprise alkyl, alkenyl or hydroxy alkyl, about 10 ethylene oxides part of 0-and about 1 the glyceryl part of 0-with about 8-18 carbon atom; Y is selected from nitrogen, p and s atom; R
3For comprising the alkyl or the monohydroxyalkyl group of about 3 carbon atoms of 1-; When Y was sulphur atom, X was 1, and when Y was nitrogen or phosphorus atoms, X was 2; R
4Be the alkylidene or the hydroxy alkylidene of about 4 carbon atoms of 1-, Z is the group that is selected from carboxylate radical, sulfonate radical, sulfate radical, phosphonate radical and phosphate radical.
The example of amphoteric surfactant and zwitterionic surfactant also comprises sulfobetaines (sultaines) and acylamino-sulfobetaines.The example that comprises the sulfobetaines of acylamino-sulfobetaines comprises: coco dimethyl propyl group sulfobetaines, stearoyl dimethyl propyl sulfobetaines, lauryl be two-(2-ethoxy) propyl group sulfobetaines etc.; And the acylamino-sulfobetaines, as cocoyl acylamino-dimethyl propyl sulfobetaines, stearyl acylamino-dimethyl propyl sulfobetaines, lauryl acylamino-two-(2-ethoxy) propyl group sulfobetaines etc.Preferably acylamino-hydroxyl sulfo betaine such as C
12-C
18Alkyl acylamino-propyl hydroxy sulfobetaines, particularly C
12-C
14Alkyl acylamino-propyl hydroxy sulfobetaines is as lauryl acylamino-propyl hydroxy sulfobetaines and cocos nucifera oil acylamino-propyl hydroxy sulfobetaines.Other sulfobetaines is at USP 3,950, states in 417, and the document is incorporated herein by reference.
Other suitable amphoteric surfactant is formula R-NH (CH
2)
nThe amino-alkane hydrochlorate of COOM, formula R-N[(CH
2)
mCOOM]
2Iminodiacetic alkanoate and its mixture; Wherein, n and m are the number of 1-4, and R is C
8-C
22Alkyl or alkenyl, M are hydrogen, alkali metal, alkaline-earth metal, ammonium or alkanol ammonium.
The example of suitable amino-alkane hydrochlorate comprises: positive alkyl aminopropionate and positive alkyl imino-diacetic propionate, its instantiation comprises N-lauryl-Beta-alanine or its salt and N-lauryl-β-imino-diacetic propanoic acid or its salt and its mixture.
Other suitable amphoteric surfactant comprises those that are expressed from the next:
Wherein, R
1Be C
8-C
22Alkyl or alkenyl, preferred C
12-C
16R
2And R
3Be independently selected from hydrogen ,-CH
2CO
2M ,-CH
2CH
2OH ,-CH
2CH
2OCH
2CH
2COOM or-(CH
2CH
2O)
mH, wherein, m is the integer of 1-about 25, R
4Be hydrogen, CH
2CH
2OH or CH
2CH
2OCH
2CH
2COOM, Z are CO
2M or CH
2CO
2M, n are 2 or 3, and be preferred 2, and M is hydrogen or cation, as alkali metal (as lithium, sodium, potassium), alkaline-earth metal (beryllium, magnesium, calcium, strontium, barium) or ammonium.The surfactant of this type also is categorized as the imidazoline type amphoteric surfactant sometimes, still, will be appreciated that, they are also nonessentially directly or indirectly obtained by the imidazoline intermediate.This type of suitable material can be purchased by trade name MIRANOL, is interpreted as comprising the compound mixture of this type of material, for R
2Material during for hydrogen, according to its pH value, they can protonated and non-protonization form existence.Plan is contained in all this variations and kind in the following formula.
The example of the surfactant of following formula is unary carboxylation and dicarboxylate.Its instantiation comprises cocos nucifera oil both sexes carboxyl propionate, cocos nucifera oil both sexes carboxyl propanoic acid, cocos nucifera oil both sexes carboxyl glycinate (also being referred to as cocos nucifera oil both sexes diacetin) and cocos nucifera oil both sexes acetate.
The amphoteric surfactant that is purchased comprises those that sell with following trade name: MIRANOLC2M CONC.N.P, and MIRANOL C2M CONC.O.P., MIRANOL C2M SF, MIRANOL CM SPECIAL (Miranol, Inc.); ALKATERIC 2CIB (AlkarilChemicals); AMPHOTERGE W-2 (Lonza, Inc.); MONATERIC CDX-38, MONATERIC CSH-32 (Mona industries); REWOTERIC AM-2C (RewoChemical Group); SCHERCOTERIC MS-2 (Scher Chemicals).
The beet alkali surface activator that is applicable to care composition of the present invention is that zwitterionic surfactant is those that are expressed from the next:
Wherein, R
1Be selected from COOM and CH (OH) CH
2SO
3M, R
2Be low alkyl group or hydroxyalkyl; R
3Be low alkyl group or hydroxyalkyl; R
4Be selected from hydrogen and low alkyl group; R
5Be senior alkyl or alkenyl; Y is a low alkyl group, preferable methyl; M is the integer of 2-7, preferred 2-3; N is integer 1 or 0; M is hydrogen or foregoing cation, as alkali metal, alkaline-earth metal or ammonium.Term " low alkyl group " or " hydroxyalkyl " are meant the radical of saturated aliphatic alkyl and the substituted hydrocarbon radical of the straight or branched with about 1-3 carbon atom, for example, and methyl, ethyl, propyl group, isopropyl, hydroxypropyl, ethoxy etc.Term " senior alkyl or alkenyl " is meant the aliphatic hydrocarbyl of the straight or branched with about 8-20 carbon atom saturated (i.e. " senior alkyl ") and unsaturated (i.e. " senior alkenyl "), for example, and lauryl, cetyl, stearyl, oil base etc.Be appreciated that term " senior alkyl or alkenyl " comprises the radical mixture that can comprise one or more intermediate chain such as ether or polyether chain or non-sense substituent such as hydroxyl or halogen, wherein, described free radical has kept hydrophobic property.
The example that is used for the surfactant betanin (n is) of following formula of the present invention at 0 o'clock comprises alkyl betaine, as coco dimethyl carboxymethyl betaine, lauryl dimethyl carboxymethyl betaine, lauryl dimethyl-α-carboxyethyl betanin, cetyl dimethyl carboxymethyl betaine, lauryl two-(2-ethoxy) carboxymethyl betaine, stearyl be two-(2-hydroxypropyl) carboxymethyl betaine, oil base dimethyl γ-carboxylic CAB, lauryl-two-(2-hydroxypropyl)-α-carboxyethyl betanin etc.Sulfobetaines be represented as coco dimethyl sulfopropyl betaine, stearoyl dimethyl sulfopropyl betaine, lauryl two-(2-ethoxy)-sulfopropyl betaine etc.
Be used for the amido betaines of care composition of the present invention and the instantiation of acylamino-sulfobetaines and comprise the acylamino-carboxybetaine, as cocos nucifera oil acylamino-dimethyl carboxymethyl betaine, lauryl acylamino-dimethyl carboxymethyl betaine, cetyl acylamino-dimethyl carboxymethyl betaine, lauryl acylamino-two-(2-ethoxy) carboxymethyl betaine, cocos nucifera oil acylamino--two-(2-ethoxy)-carboxymethyl betaine etc.The representative of acylamino-sulfobetaines is cocos nucifera oil acylamino-dimethyl sulfopropyl betaine, stearyl acylamino-dimethyl sulfopropyl betaine, lauroyl amino-two-(2-ethoxy)-sulfopropyl betaine etc.
Non-ionic surface active agent
Wo 2008069000 of the present invention can comprise a kind of non-ionic surface active agent.Non-ionic surface active agent is selected from by hydrophilic oxyalkylene compounds and can is the condensation product of the hydrophobic organic compound of aliphatic or alkyl aromatic.
The unrestricted example of non-ionic surface active agent preferred for the present invention is:
(1) polyethylene oxide condensation compound of alkyl phenol, comprise about 6-20 carbon atom and be the alkyl phenol of straight or branched configuration and the condensation product of oxirane as alkyl group, the consumption of described oxirane is about 60 moles of ethylene oxide of about 10-/mole alkyl phenol;
(2) oxirane carries out the material that condensation obtains with the product that is formed by expoxy propane and reacting ethylenediamine;
(3) have about 18 carbon atoms of about 8-and be the aliphatic alcohol of straight or branched configuration and the condensation product of oxirane, as the cocoanut oil alcohol ethylene oxide condensate that every mole of coco alcohol has about 30 moles of ethylene oxide of about 10-, cocoanut oil alcohol partly has about 14 carbon atoms of about 10-;
(4) formula [R
1R
2R
3N → O] the long chain tertiary amine oxide, wherein, R
1Comprise alkyl, alkenyl or monohydroxy alkyl, and have about 10 the ethylene oxide parts of 0-, about 1 the glyceryl part of 0-, R with about 18 carbon atoms of about 8-
2And R
3Comprise about 3 carbon atoms of about 1-and about 1 hydroxyl of 0-, as methyl, ethyl, propyl group, ethoxy or hydroxypropyl;
(5) the long chain tertiary phosphine oxide of formula [RR ' R " P → O]; wherein; R comprises and has the alkyl that chain is about about 18 carbon atoms of 8-; alkenyl or monohydroxy alkyl; and have about 10 the ethylene oxide parts of 0-; about 1 the glyceryl part of 0-, R ' and R " are alkyl or the monohydroxy alkyl that contains about 3 carbon atoms of the 1-that has an appointment;
(6) long-chain dialkyl sulphoxide, it comprises a short-chain alkyl or a hydroxy alkyl (normally methyl) with about 3 carbon atoms of 1-, also comprise a long-chain hydrophobic chain, comprise the alkyl, alkenyl, hydroxy alkyl or the ketone group alkyl that contain about 20 carbon atoms of the 8-that has an appointment, about 10 the ethylene oxide parts of 0-, about 1 the glyceryl part of 0-;
(7) alkyl polysaccharide (APS) surfactant (as alkyl polyglucoside), the example be at US 4,565, states in 647, and the document is incorporated herein by reference; The document discloses the APS surfactant, and it has the hydrophobic group of about 30 carbon atoms of about 6-and as the polysaccharide group (as poly glucoside) of hydrophilic group; Randomly, exist the polyalkylene oxide group that hydrophobicity is connected with hydrophilic parts; And that alkyl group (being hydrophobic parts) can be is saturated or undersaturated, side chain or (for example replacing with hydroxyl or ring) non-side chain, that do not replace or replace; Preferred material is an alkyl polyglucoside, and it is commercially available from Henkel, ICI Americas, and Seppic; With
(8) suc as formula RO (CH
2CH
2)
nThose polyoxyethylene alkyl ethers of H and suc as formula R (O) OCH
2CH (OH) CH
2(OCH
2CH
2)
nThose Polyethylene Glycol (PEG) fatty acid glyceride of OH, wherein, n is that 1-is about 200, and preferably about 20-is about 100, and R is the alkyl with about 22 carbon atoms of about 8-.
Other optional ingredient
Multiple additional composition can be formulated in the compositions of the present invention.These supplementary elements comprise: other conditioner such as hydrolytic collagen, hydrolysis of keratin, protein, plant extract and nutrient; Hair keeps polymer; Other surfactant such as anion surfactant; Additional thickening agent and suspending agent such as xanthan gum, guar gum, hydroxyethyl-cellulose, methylcellulose, starch and starch derivatives; The methanol amide such as the coconut monoethanol amide of viscosity modifier such as long-chain fatty acid; Pearlescent additive such as diglycol stearate; Antiseptic such as benzylalcohol, methyl parahydroxybenzoate, propyl p-hydroxybenzoate and imidazolidinyl urea; Solvent such as polyvinyl alcohol, ethanol, volatility and nonvolatile low-molecular-weight siloxane fluid; PH regulator agent such as citric acid, sodium citrate, succinic acid, phosphoric acid, sodium hydroxide, sodium carbonate; Salt, generally for example potassium acetate and sodium chloride; Coloring agent such as FD﹠amp; C or D﹠amp; The C dyestuff; Hair oxidation (bleaching) agent is as hydrogen peroxide, perborate and persulfate; Hair Reducing agent such as thioglycolate salt; Spice; Sequestering agent such as disodiumedetate; Polymeric plasticizer such as glycerol, dibutyl adipate, butyl stearate and propylene glycol; Ultraviolet and infrared ray screening agent and absorbent such as ethylhexyl salicylate and propellant such as fluorohydrocarbon, dimethyl ether, CO
2, nitrogen and LPG gas.Usually these selectivity compositions use amount separately is about 0.01% to about 10.0%, preferred about 0.05% to about 5.0% of a composition weight.
Using method
Use Wo 2008069000 of the present invention so that conditioning effect such as wettability, flexibility, free mobility to be provided with conventional method, viscosity reduces, and static is controlled.This using method depends on the type of the compositions of use, but the product with effective dose is coated on the hair usually, it can be rinsed (as under the situation of using hair conditioner) from hair then, or make it be retained in (as under the situation of hair jelly, surfactant, hair spray, mousse and hair cream) on the hair." effective dose " means the consumption that is enough to provide conditioning effect.Usually, about 1-50 gram Wo 2008069000 is coated on hair and/or the scalp.If compositions is inhomogeneous, as be separated into biphasely, need before use compositions to be mixed.Compositions all over being applied on the hair, is rubbed or massage hair or scalp usually.Preferably, before the hair drying, compositions is coated on the moistening or moist hair.After being coated to this based composition on the hair, that hair is dry and according to the hobby shaping hair of user.Perhaps, compositions is coated on the hair, then combing hair and according to the hobby shaping hair of user.
Embodiment
The following examples are further set forth and the interior technical scheme of the explanation scope of the invention.These embodiment only are in order to set forth purpose of the present invention, are not limitation of the present invention, because multiple variation can be arranged not breaking away under spirit of the present invention and the category.The title of each composition is with chemical name or the definition of CTFA title, perhaps with following title definition.
Unless stipulate that in addition hair conditioning composition of the present invention is represented with the percetage by weight of whole compositions.
Composition shown in below can preparing with conventional method known in the art.Suitable method and composition is as follows:
Example I-VI
For example I-V.I, 70 ℃ of of stirrings of under, the mixture of stearyl trimethyl ammonium chloride, L-glutamic acid and MATMAC is joined in the distilled water.Then, 60 ℃ of under agitation add octadecanol and spermol.After being cooled to below, other composition that removes denatured ethyl alcohol and spice being added in the above-mentioned solution, 50 ℃ of of mixture of and stir.At that cool off gained down, add denatured ethyl alcohol and spice.The compositions of gained provides slickness and soft feeling to hair. embodiment sequence number I II III IV V VI four isostearic acid pentaerythritol esters 0.5-0.25-0.25-three isostearic acids trihydroxymethylpropanyl ester-0.5-0.25-0.5 nutmeg methyl esters 0.5-0.4---oleyl alcohol---the amino propyl-dimethyl amine 2.0 2.0 3.0 2.0-2.0L-of 0.4-mineral oil---0.3-isostearic acid octyl group dodecane ester-0.3-0.25-0.3 octadecanol 4.0 2.8 2.0 2.8 4.0-cetanol 6.0 4.2 3.0 4.2 3.0 7.0 solid paraffins-1.0-1.0--stearoyl glutamic acid 0.64 0.64 1.0 0.64-0.64MATMAC* 1----0.25-mixture of siloxanes
* 25.0 1.0-1.0 2.0 4.0 antiseptic, 0.2 0.3 0.2 0.25 0.1 0.5 spice, 0.2 0.25 0.1 0.2 0.4 0.2 denatured ethyl alcohols----10.0-water adds to 100%
* 1MATMAC: have C
20-C
22The monoalkyl trimethyl ammonium chloride of alkyl
* 2 mixture of siloxanes: the D5 Cyclomethicone of 85%/15% (weight ratio) and the mixture of polydimethylsiloxane sizing material (weight average molecular weight is about 400,000-600,000).
For example VII A-X; Under agitation, all components is joined in the denatured ethyl alcohol.The compositions of gained is packed in the packing that flusher is housed to make the conditioning spray.The compositions of gained provides slickness and soft feeling to hair. embodiment VII VIII IX X four isostearic acid pentaerythritol ester 1.50--0.5 three isostearic acid trihydroxymethylpropanyl ester-1.0 1.5-nutmeg methyl esters 1.50 1.0--oleyl alcohol---0.5 mineral oil--1.5-cetanol-1.0--MATMAC* 1-0.2-0.2 antiseptic 0.1 0.1 0.1 0.1 spice 0.1 0.1 0.1 0.1 denatured ethyl alcohols add to 100%
* 1MATMAC: have C
20-C
22The monoalkyl trimethyl ammonium chloride of alkyl.
Claims (5)
1. Wo 2008069000 comprises:
(a) oily compound of water-insoluble high molecular weight, its molecular weight is at least 800, proportion at least 0.9, be in a liquid state at 25 ℃, and it is selected from four isostearic acid pentaerythritol esters, three isostearic acid trihydroxymethylpropanyl esters, four pentaerythritol oleates, three oleic acid trihydroxymethylpropanyl esters and composition thereof;
(b) fat tertiary amine of acylamino-replacement, it is selected from: the amino propyl-dimethyl amine of stearoyl, the amino propyl group diethylamide of stearoyl, the amino ethyl diethylamide of stearoyl, the amino ethyl dimethyl amine of stearoyl, palmityl aminopropyl dimethyl amine, palmityl aminopropyl diethylamide, palmityl amino-ethyl diethylamide, palmityl amino-ethyl dimethyl amine, docosyl acylamino-propyl-dimethyl amine, docosyl acylamino-propyl group diethylamide, docosyl acylamino-ethyl diethylamide, docosyl acylamino-ethyl dimethyl amine, eicosyl acylamino-propyl-dimethyl amine, eicosyl acylamino-propyl group diethylamide, eicosyl acylamino-ethyl diethylamide, eicosyl acylamino-ethyl dimethyl amine, diethylamino ethyl stearmide;
(c) L-glutamic acid; With
(d) carrier.
2. Wo 2008069000 according to claim 1, also comprise a kind of additional conditioner, be selected from the low-molecular-weight oily compound of nonvolatile water-insoluble, the insoluble aliphatic compound of solid water, cationic surfactant, cationic polymer, polysiloxane compound and its mixture.
3. Wo 2008069000 according to claim 2, wherein nonvolatile water-insoluble low-molecular-weight oily compound are selected from isostearic acid octyl group dodecyl ester, isostearic acid methyl ester, oleyl alcohol, have the hydrocarbon of 10-40 carbon atom, and composition thereof.
4. Wo 2008069000 according to claim 2, wherein the insoluble aliphatic compound of solid water is selected from the hydrocarbon that has 20 carbon atoms at least, saturated fatty alcohol, fatty acid, derivative of fatty acid, fatty alcohol derivative, steroid and composition thereof.
5. Wo 2008069000 according to claim 4, wherein the insoluble aliphatic compound of solid water is selected from and has C
14-C
22Saturated fatty alcohol.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN 96180564 CN1120701C (en) | 1996-12-06 | 1996-12-06 | Hair conditioning compositions comprising water-insoluble high molecular weight oily compound |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN 96180564 CN1120701C (en) | 1996-12-06 | 1996-12-06 | Hair conditioning compositions comprising water-insoluble high molecular weight oily compound |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN1241933A CN1241933A (en) | 2000-01-19 |
| CN1120701C true CN1120701C (en) | 2003-09-10 |
Family
ID=5127995
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN 96180564 Expired - Fee Related CN1120701C (en) | 1996-12-06 | 1996-12-06 | Hair conditioning compositions comprising water-insoluble high molecular weight oily compound |
Country Status (1)
| Country | Link |
|---|---|
| CN (1) | CN1120701C (en) |
-
1996
- 1996-12-06 CN CN 96180564 patent/CN1120701C/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| CN1241933A (en) | 2000-01-19 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CN1120703C (en) | Conditioning shampoo compositions containing select hair conditioning agents | |
| CN1181812C (en) | Mousse-forming shampoo compsns. | |
| CN1245948C (en) | Stabilized hair care products | |
| CN1104881C (en) | Conditioning shampoo compositions containing select hair conditioning osters | |
| CN1142769C (en) | Personal cleansing compositions | |
| CN1044087C (en) | Shampoo composition with silicone, cationic polymer, and oily liquid conditioning agents | |
| CN1197543C (en) | Conditioning shampoo compositions | |
| JP2000513379A (en) | Conditioning shampoo composition | |
| CN1256623A (en) | Hair treatment compositions | |
| CN1925837A (en) | Mild, viscous cleansing composition with versatile compatibility and enhanced conditioning | |
| CN1239880A (en) | Styling shampoo compositions with improved styling polymer deposition | |
| CN1372455A (en) | Hair conditioning composition comprising hydrophobically modified cellulose ether | |
| CN101040825A (en) | Hair cleansing composition | |
| JP2000513387A (en) | Conditioning shampoo composition | |
| CN1278718A (en) | Conditioning shampoo composition comprising pentaerythritol ester oil | |
| CN1306412A (en) | Hair conditioning compsn. comprising poly & Alpha,-olefin oil | |
| CN100335031C (en) | Hair conditioning compositions | |
| CN1418082A (en) | Hair care composition containing polyalkyleneglycol (n) dlkylamine | |
| CN1372456A (en) | Hair conditioning composition comprising cationic silicone emulsion | |
| CN1391461A (en) | Hair conditioning composition comprising hydrophobically modified cationic cellulose | |
| CN1182827C (en) | Hiar treatment compositions | |
| CN1279600A (en) | Conditioning shampoo composition comprising pantaerythritol ester oil | |
| CN1120701C (en) | Hair conditioning compositions comprising water-insoluble high molecular weight oily compound | |
| CN1286612A (en) | Conditioning shampoo compositions | |
| CN1870973A (en) | Antidandruff shampoo composition |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| C06 | Publication | ||
| PB01 | Publication | ||
| C10 | Entry into substantive examination | ||
| SE01 | Entry into force of request for substantive examination | ||
| C10 | Entry into substantive examination | ||
| SE01 | Entry into force of request for substantive examination | ||
| C14 | Grant of patent or utility model | ||
| GR01 | Patent grant | ||
| C19 | Lapse of patent right due to non-payment of the annual fee | ||
| CF01 | Termination of patent right due to non-payment of annual fee |