CN1203840C - Cleaning compositions - Google Patents
Cleaning compositions Download PDFInfo
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- CN1203840C CN1203840C CNB008042462A CN00804246A CN1203840C CN 1203840 C CN1203840 C CN 1203840C CN B008042462 A CNB008042462 A CN B008042462A CN 00804246 A CN00804246 A CN 00804246A CN 1203840 C CN1203840 C CN 1203840C
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q19/00—Preparations for care of the skin
- A61Q19/10—Washing or bathing preparations
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
- A61K8/81—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
- A61K8/34—Alcohols
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
- A61K8/34—Alcohols
- A61K8/347—Phenols
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/40—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
- A61K8/42—Amides
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/40—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
- A61K8/44—Aminocarboxylic acids or derivatives thereof, e.g. aminocarboxylic acids containing sulfur; Salts; Esters or N-acylated derivatives thereof
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/40—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
- A61K8/44—Aminocarboxylic acids or derivatives thereof, e.g. aminocarboxylic acids containing sulfur; Salts; Esters or N-acylated derivatives thereof
- A61K8/442—Aminocarboxylic acids or derivatives thereof, e.g. aminocarboxylic acids containing sulfur; Salts; Esters or N-acylated derivatives thereof substituted by amido group(s)
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/46—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing sulfur
- A61K8/463—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing sulfur containing sulfuric acid derivatives, e.g. sodium lauryl sulfate
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/46—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing sulfur
- A61K8/466—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing sulfur containing sulfonic acid derivatives; Salts
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
- A61K8/81—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
- A61K8/8105—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
- A61K8/8111—Homopolymers or copolymers of aliphatic olefines, e.g. polyethylene, polyisobutene; Compositions of derivatives of such polymers
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q13/00—Formulations or additives for perfume preparations
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q17/00—Barrier preparations; Preparations brought into direct contact with the skin for affording protection against external influences, e.g. sunlight, X-rays or other harmful rays, corrosive materials, bacteria or insect stings
- A61Q17/005—Antimicrobial preparations
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q17/00—Barrier preparations; Preparations brought into direct contact with the skin for affording protection against external influences, e.g. sunlight, X-rays or other harmful rays, corrosive materials, bacteria or insect stings
- A61Q17/02—Barrier preparations; Preparations brought into direct contact with the skin for affording protection against external influences, e.g. sunlight, X-rays or other harmful rays, corrosive materials, bacteria or insect stings containing insect repellants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q17/00—Barrier preparations; Preparations brought into direct contact with the skin for affording protection against external influences, e.g. sunlight, X-rays or other harmful rays, corrosive materials, bacteria or insect stings
- A61Q17/04—Topical preparations for affording protection against sunlight or other radiation; Topical sun tanning preparations
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q5/00—Preparations for care of the hair
- A61Q5/02—Preparations for cleaning the hair
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- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Epidemiology (AREA)
- Birds (AREA)
- Dermatology (AREA)
- Emergency Medicine (AREA)
- Pest Control & Pesticides (AREA)
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- Cosmetics (AREA)
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Abstract
A rinse-off liquid personal cleansing composition comprising (a) water; (b) from about 1% to about 60% by weight of a water-soluble surfactant, (c) a water-insoluble oil selected from highly branched polyalphaolefins having formula (1): wherein R<1> is H or C1-C20 alkyl, R<4> is C1-C20 alkyl, R<2> is H or C1-C20, and R<3> is C3-C20 preferably from C5-C20, n is an integer from 0 to 3 and m is an integer of from 1 to about 1000 and having a number average molecular weight of from about 1000 to about 25,000; and (d) a hydrophobic skin active component selected from antimicrobial agents, sunscreens, vitamins, perfume oils insect repellants, anti-fungal agents, and mixtures thereof, wherein the hydrophobic skin active component has a ClogP value of greater than 3. The personal cleansing compositions of the invention provide improved deposition of hydrophobic skin actives, excellent rinse feel and skin mildness.
Description
Technical field
The present invention relates to Cleasing compositions.The invention particularly relates to gentle personal cleaning compositions, said composition demonstrates for example deposition of the improvement of antimicrobial, sunscreen and vitamin of skin care actives.In addition, compositions of the present invention also demonstrates cleaning sense and the advantages of good skin tactility and the foaminess of improvement, they are suitable for cleaning simultaneously and conditioning skin and/or hair, for example can foam bathing goods, shower product, skin cleaner, hands, face and forms such as clean body agent, shampoo use.
Background of invention
Gentle cosmetic composition must satisfy the multiple standards that comprises cleaning power, foaminess and mildness/low irritant/advantages of good skin, hair and eye mucosa sensation.Skin is by covering and protecting several confluent monolayer cells of lower-hierarchy to constitute.Keratin and collagen fiber albumen form its structural framework.The outermost layer of these layers is called as horny layer.Equally, hair also has the protective garments around hair fiber, is called as cuticula (horny layer).Anion surfactant can penetrate cutin tunic and cuticula, and destroys the integrity of film by degreasing, makes it lose barrier action and water retaining function.
This interference effect for skin and hair protecting film can cause coarse skin sense and eye to stimulate, and finally impels surfactant to cause immunoreation and produces stimulation.
Ideal cosmetic cleaning agent is cleaning skin or hair leniently, and should not make hair and skin defat and/or dry, does not stimulate the eye mucosa or can not make skin tight after daily use simultaneously.Great majority foaming soap, shower and bathing product, shampoo and block cleaning product can not satisfy these requirements.
Known some synthetic surfactant is gentle.But when preparation shampoo and personal cleanser, a major defect of the synthetic surfactant system that some is gentle is to have the cleaning sense of not liking for some client that can be described as " smooth " or " not having puckery sense ".On the other hand, some surfactant for example use of potassium laurate can produce the cleaning sense of " puckery sense ", but damages clinical skin mildness.The both of these case explanation must be carried out balance between cleaning sense and mildness when selecting suitable surfactant.
Therefore, still need to have the personal cleaning compositions that " puckery sense " cleans sense, said composition is removed has good product attribute, for example foams, cleans, stablizes, outside thickening, rheological characteristic and the skin usability, also has the advantages of good skin mildness.
Also wish to make the skin care activity composition offer skin from personal cleaning compositions.This class skin care activity composition comprises, for example sunscreen, antimicrobial and vitamin.Past attempts attempts providing skin care actives from personal cleaning compositions.Yet, based on these active substance capacities be deposited on the skin could the generation effect viewpoint, these trials always can not succeedd.
WO 97/16168 discloses a kind of personal cleaning compositions; contain (a) surfactant; (b) hydrophobic active composition; be selected from: skin conditioning agent, skin care and antibacterial; (c) composition of hydrocarbonaceous and (d) cationic polymer are selected (c) and amount (d) so that component (b) is higher than (c) and (d) independent adduction to the effect of skin.
Unexpectedly find now, by some water-insoluble oil, for example some poly ﹠ Alpha ,-olefin oil and some hydrophobicity skin care activity composition and gentleness, water soluble surfactant active's system combines, and can be provided at the personal cleaning compositions of the deposition with improvement of sending out the cleaning sense puckery and also having the hydrophobicity skin care actives good gentle characteristic the time.
Summary of the invention
The invention provides a kind of liquid personal cleansing composition of washing off, contain:
(a) water;
(b) water soluble surfactant active of about 1%-about 60% (weight);
(c) water-insoluble oil is selected from the highly branched poly alpha olefin of following formula
R wherein
1Be H or C
1-C
20Alkyl, R
4Be C
1-C
20Alkyl, R
2Be H or C
1-C
20Alkyl, R
3Be C
3-C
20Alkyl, preferred C
5-C
20Alkyl, n are the integer of 0-3 and the integer that m is 1-1000, and the about 1000-of number-average molecular weight about 25000; With
(d) hydrophobicity skin care activity composition is selected from antimicrobial, sunscreen, vitamin, aromatic oil, anthelmintic, antifungal and their mixture, and wherein the ClogP value of hydrophobicity skin care activity composition is greater than 3.
Compositions of the present invention has been improved the deposition of skin care activity composition in to the skin abnormality gentleness, have the cleaning sense of " sending out puckery ".
Except as otherwise noted, all concentration of the present invention and ratio are all in the weight of Cleasing compositions.Except as otherwise noted, the chain length of surfactant is also based on weight average chain length.
Detailed Description Of The Invention
The liquid cleansing composition of this paper contains water, surfactant, hydrophobicity skin care activity composition and some water-insoluble oil, will further describe them below.
The term that this paper adopts " cleans sense " and is meant with after the Cleasing compositions cleaning sensation of skin the flush away foam process from skin.The type of the cleaning sense that compositions of the present invention produces can be described with following term: for example " puckery sense " clean sense, " soap sample " and clean sense and " not smooth " or " sticking " and (non-slimy) clean sense.This " puckery sense ", " soap sample ", " not smooth " or " sticking " are cleaned to feel increasing by the friction between hands and the skin in the foam process on the cleaning skin and discover.
The term " water-insoluble " (oil) that this paper adopts is meant under the room temperature, under the situation that does not add other adjuvant for example as herein described and/or composition, is insoluble to the material of distilled water basically.
The term " hydrophobicity " (skin care activity composition) that this paper adopts is meant with its water solublity to be compared, easier to be liposoluble, promptly non-water-soluble material.Preferably dissolubility is very low and be (with ionic relative) material of nonionic basically in water.
Water-insoluble oil
Be used for the highly branched poly alpha olefin that water-insoluble oil of the present invention is selected from (a) following formula
R wherein
1Be H or C
1-C
20Alkyl, R
4Be C
1-C
20Alkyl, R
2Be H or C
1-C
20Alkyl, R
3Be C
3-C
20Alkyl, preferred C
5-C
20Alkyl, n are the integer of 0-3 and the integer that m is 1-1000, have about 1000-25000, preferably about 2500-6000, the more preferably from about number-average molecular weight of 2500-4000.Under 40 ℃, adopt ASTM D-445 viscosity measurement, be used for poly alpha olefin of the present invention (a) and preferably have about 300cst to about 50,000cst, preferably about 1000cst is extremely about 12,000cst, more preferably from about the 1000cst viscosity of about 4000cst extremely.(a) oil of type also can have degree of unsaturation, but preferably saturated.
Above-mentioned suitable poly alpha olefin (a) can be by having about 4-20 carbon atom, preferably about 6-12 carbon atom, and the 1-chain alkene monomer of especially about 8-12 carbon atom obtains.Be used for the preferably hydrogenant poly alpha olefin polymer of poly alpha olefin of the present invention.
The monomeric limiting examples of 1-alkene that is used to prepare poly alpha olefin polymer of the present invention comprises the 1-hexene, the 1-octene, and 1-decene, the 1-dodecylene, tetradecene, their branched chain isomer, 4-methyl-1-pentene for example, and composition thereof.What be suitable for preparing polyolefin liquid also has the 1-hexene to cetene and composition thereof, and more preferably the 1-octene is to 1-dodecylene or its mixture.
The example of this class oil comprises poly decene oil, for example by Mobil Chemical Company (P.O.Box 3140, Edison, New Jersey 08818 is USA) with Puresyn 40 and those commercially available products of Puresyn 100 trade names.
The viewpoint of improving based on the cleaning sense of compositions, particularly preferably be highly branched (a) type poly alpha olefin material, its number-average molecular weight is about 100cst about 2000cst (ASTM D-445 is in 45 ℃ of mensuration) extremely for about 2500-4000 and viscosity, for example by Mobil with the commercially available product of trade name Puresyn 100.
The mixture of above-mentioned oil also is applicable to the present invention.
In preferred embodiments, the number average bead diameter that is used for water-insoluble oil of the present invention is at about 1 micron-500 microns, preferably about 5-200 micron, 5-50 micron more preferably from about, especially preferably about 5-20 micron.
Compositions of the present invention preferably contains the 0.1%-20% that has an appointment, 0.5%-10% more preferably from about, the water-insoluble oil of especially preferably about 1%-5% (weight).
Hydrophobicity skin care activity composition
Compositions of the present invention contains and accounts for the preferably about 0.01%-10% of composition weight, more preferably from about 0.01%-5%, especially preferably the hydrophobicity skin care activity composition of about 0.1%-3%.
Be applicable to that hydrophobicity skin care actives of the present invention comprises antimicrobial, sunscreen, vitamin, aromatic oil, anthelmintic, antifungal and their mixture.
According to its octanol/water partition coefficient (P or K
Ow) can select to be applicable to hydrophobicity skin care actives of the present invention.K
OwProvide chemical substance oil loving estimated value.K
OwBe in the balance binary system of capryl alcohol-water, material is at concentration and its ratio in the concentration of aqueous phase of n-octyl alcohol in mutually.At the bottom of its logarithm to be 10 logarithm, promptly the logP form provides the partition coefficient of hydrophobicity skin care actives of the present invention easily.
" logP " can measure (MlogP) by experiment or can calculate (ClogP).For example, the ClogP value can adopt Biobyte (Claremont, CA, " ClogP forWindows " software USA) or employing Advanced Chemistry Development Inc. (Toronto, Ontario, Canada) ACD/LogP Calculator program is calculated.The Biobyte program also comprises the logP value of some available mensuration.Those of ordinary skills are clear, are difficult to the logP value that obtains to calculate for some chemical substance, in this case, and available measurement logP value.On the contrary,, be difficult to obtain to measure the logP value for some chemical substance, in this case, available calculating logP value.Measure the logP value and it has been generally acknowledged that to have comparability with calculating logP value.
Be applicable to that hydrophobicity skin care actives of the present invention is selected from the ClogP value greater than 3, is preferably greater than 5 hydrophobicity skin care actives.The ClogP value of hydrophobicity skin care actives preferably is not more than 20.
The example that can be used for suitable antibacterial of the present invention includes but not limited to diphenylcarbamide (dicarbanilide) (for example neko is also referred to as trichlorocarbanilide), Triclosan, hexachlorophene and 3,4,5-tribromsalan.The preferred antibacterial of the present invention is a neko.
The example that is used for suitable sunscreen of the present invention includes but not limited to octyl dimethyl p-aminobenzoic acid, 3,3,5-trimethylcyclohexyl salicylate (homosalate), 2-hydroxyl-4-methoxyl group-benzophenone (benzophenone-3), butyl methoxydibenzoylmethise, octyl methoxycinnamate, 4-methoxyl group-2,2 '-dihydroxy benzophenone (dioxybenzone), dihydroxy dimethoxy benzophenone (benzophenone-6), S-guaiazulene, 2-cyano group-3,3-diphenylacrylate ester-2-ethyl hexyl ester (octocrylene) and their mixture.The preferred sunscreen of the present invention is an octyl methoxycinnamate.
The example that is used for suitable vitamin of the present invention includes but not limited to vitamin A and ester, vitamin E and ester thereof, vitamin D and vitamin K and their mixture.
The example that is applicable to anthelmintic of the present invention includes but not limited to dibutyl phthalate.
The example that is used for suitable aromatic oil of the present invention includes but not limited to that ambrettolide is (available from International Flavors ﹠amp; Fragrances (IFF), Liebegerweg72-98,1221 JT Hilversum, The Netherlands), Ambrinol T is (available from Takasago International Corp. (USA), 11 Volvo Drive, Rockleigh, NJ 07647-0932, USA), benzyl salicylate, geraniol acetate, damascenone is (available from Firmenich SA, 1, Route des Jeunes, CH-1211 Geneva 8, Switzerland, Habanolide (Firmenich), ionoionone γ Methyle (available from Givaudan-Roure, 19-23 voie des Bans, BP98,95101 Argenteuil Cedex France), ionoionone β (available from Givaudan-Roure), Norlimbanol (Firmenich), Sanjinol (IFF), Undelactone gamma (available from Givaudan-Roure), vetacetyl (available from Bonpard, HGH Fragrance Resources, Borstelmannsweg 169, D-20537 Hamburg, Germany), vertofix coeur (IFF) and their mixture.
The example that is used for suitable antifungal of the present invention includes but not limited to butoben, hexachlorophene, CF3,9-undecylenic acid and ester thereof and their mixture.
Being used for particularly preferred hydrophobicity skin care actives of the present invention is antimicrobial, vitamin and derivant thereof and sunscreen, especially antimicrobial, particularly neko.
Surfactant system
As another basic feature, compositions of the present invention contains water soluble surfactant active's surfactant system.Define as the present invention, the water soluble surfactant active is meant molecular weight less than about 20,000 surfactant, and wherein described surfactant can form transparent isotropic aqueous solution with 0.2%w/w concentration when water-soluble under indoor conditions.Be applicable to that the surfactant that is included in the present composition has the lipophile chain of chain length for about 6-22 carbon atom usually, can be selected from anionic property, nonionic, amphion and amphoteric surfactant and their mixture.The total content of surfactant is preferably about 2%-40%, 3%-25% (weight) more preferably from about, especially about 5%-20% (weight).Described compositions preferably contains the mixture of anion surfactant and amphion and/or amphoteric surfactant.Anion surfactant: the weight ratio of amphion and/or amphoteric surfactant is about 1: 10-10: 1, preferred about 1: 5-5: 1, more preferably from about 1: 3-3: 1.The compositions that in the scope of the invention other is fit to comprises the mixture of anion surfactant, amphion and/or amphoteric surfactant and one or more non-ionic surface active agents.
Compositions of the present invention can contain the 0.1%-25% that has an appointment, 1%-20% more preferably from about, the water soluble anionic surfactant of especially about 5%-15% (weight).
Be applicable to that the water soluble anionic surfactant in the present composition comprises alkyl sulfate; the alkyl sulfate of ethoxylation; alkyl ethoxy carboxylate; alkyl glycerol ether sulfonate; the ethyoxyl ether sulfonate; methyl-acyl taurine salt; fat acidyl glycine salt; the N-acyl glutamate; acyl-hydroxyethyl sulfonate; alkyl sulfo succinate; the alkyl ethoxy sulfosuccinate; α-alpha-sulfonated fatty acid; their salt and/or their ester; alkyl phosphate, the alkyl phosphate of ethoxylation, acyl sarcosinates and fatty acid/protein condensation substance; soap class (lauric acid for example; the ammonium salt of myristic acid and Palmic acid; magnesium salt; potassium salt; triethanolamine salt and sodium salt); acylaspartic acid salt, alkoxyl coconut oleoyl amine carboxylate, (ethoxylation) alkanolamide sulfosuccinate; the alkyl citric acid sulfosuccinate of ethoxylation; the acyl group ethylene diamine triacetate, acyl group ethoxy isethionate, amide alkoxy sulfate; linear alkylbenzene sulfonate (LAS); paraffin sulfonate, alpha-alkene sulfonate, alkyl alkoxy sulfate and their mixture.The alkyl of these surfactants and/or acyl group chain length are C
6-C
22, preferred C
12-C
18, more preferably C
12-C
14
Other water soluble anionic surfactant that is applicable to the present composition is 1 mole of high fatty alcohol and the salt of the sulfuric ester of the product of the oxirane of about 1-12 mole, and preferably counter ion counterionsl gegenions are sodium, ammonium and magnesium.Particularly preferably be and contain about 2-6, the alkyl ethoxy sulfate of the oxirane of preferred 2-4 mole, lauryl ether-2 sodium sulfate for example, lauryl ether-3 sodium sulfate, lauryl ether-3 ammonium sulfate and lauryl ether-3.6 sodium sulfate magnesium.In preferred embodiments, anion surfactant contains at least about 50%, especially at least about the alkyl sulfate of the ethoxylation of 75% (weight).
Except the alkyl sulfate of the ethoxylation of the wide region that obtains by the catalytic ethoxylation technology of conventional sodium and sulphation technology subsequently, the alkyl sulfate of the ethoxylation that is obtained by the ethoxylate (NRE) of close limit also is the water soluble anionic surfactant that is applicable to the present composition.The alkyl sulfate that is applicable to the ethoxylation of close limit of the present invention is selected from and on average contains about 1-6, the sulphation alkyl ethoxylate of preferably about 2-4, especially 3 moles of ethylene oxide, for example NRE lauryl ether-3 sodium sulfate.Be applicable to that NRE material of the present invention has following desired oxirane (EOn) and distributes: the EOn of 15%-about 30% (weight), the EO of about 10%-20% (weight)
N+1EO with about 10%-20% (weight)
N-1Highly preferred NRE material contains have 7 moles or more than the alkyl sulfate of the ethoxylation of 7 moles oxirane with less than the alkyl sulfate of the non-ethoxylatedization of about 13% (weight) less than about 9% (weight).Suitable lauryl ether 3 sulfate NRE materials can be available from Hoechst, its commodity GENAPOL ZRO Narrow Range by name and GENAPOL Narrow Range.
Compositions of the present invention can comprise the alkyl ethoxy carboxylate surfactant as water soluble anionic surfactant, and its content is about 0.5%-15%, preferably about 1%-10%, 1%-6% more preferably from about, especially about 1%-4% (weight).In compositions of the present invention, alkyl ethoxy carboxylate surfactant is extremely important for advantages of good skin mildness and good cleaning performance and ideal foaminess are provided.
Be applicable to that alkyl ethoxy carboxylate of the present invention has the structure of general formula (I):
R
3O(CH
2CH
2O)kCH
2COO-M+
R wherein
3Be C
10-C
16Alkyl or alkenyl, preferred C
11-C
15, more preferably C
12-C
14Alkyl or C
12-C
13Alkyl, k is 2-about 7, preferred about 3-6,3.5-5.5 more preferably from about, especially about 4-5, most preferably from about the ethoxylation meansigma methods of 4-4.5, and M is a water-soluble cationic, preferred as alkali, alkaline-earth metal, ammonium, low-level chain triacontanol ammonium and, two and triethanol ammonium, more preferably sodium, potassium and ammonium, most preferably sodium, ammonium and with the mixture of magnesium and calcium ion.
Be applicable to that particularly preferred water soluble anionic surfactant of the present invention is the alkyl ethoxy carboxylate surfactant with selected alkyl chain length and/or ethoxylate distribution.Therefore, the alkyl ethoxy carboxylate surfactant that is applicable to the present composition can have R
3And/or the different distribution of the meansigma methods of k.
As average R
3Be C
11, C
12, C
13Or C
14The time, the meansigma methods of k is generally about 3-6.Be applicable to that preferred water soluble anion alkyl ethoxy carboxylate surfactant of the present invention is C
12-C
14(average EO 3-6) ethoxy carboxylate and C
12-C
13(average EO 3-6) ethoxy carboxylate.Suitable material comprises can be available from Shell Inc. (Houston, Texas, the salt of NEODOX 23-4 (RTM) USA) and EMPICOL (RTM) CBCS (Albright ﹠amp; Wilson).Be used for highly preferred alkyl ethoxy carboxylate surfactant of the present invention, work as R
3Be C
12-C
14Or C
12-C
13During alkyl, the meansigma methods of k is about 3-6,3.5-5.5 more preferably from about, especially about 4-5, most preferably from about 4-4.5.
In preferred embodiments, described compositions is substantially free of the soap class, and promptly they contain less than about 5%, preferably less than about 1%, and the soap class of preferred 0% (weight).
Compositions of the present invention also can contain the 0.1%-20% that has an appointment, more preferably 0.1%-10%, the water soluble nonionic surfactant of especially about 1%-8% (weight).This class surfactant comprises sucrose polyfatty acid esters surfactant, C
10-C
18The polyhydroxy fatty acid amide surfactants of APG and general formula (III).
In N-alkyl, N-alkoxyl or the N-aryloxy polyhydroxy fatty acid amide surfactants of preferred formula (III), R
8Be C
5-C
31Alkyl, preferred C
6-C
19Alkyl comprises straight chain and branched alkyl and alkenyl or their mixture; R
9Normally hydrogen, C
1-C
8Alkyl or hydroxyalkyl, preferable methyl, perhaps R
9Be formula-R
1-O-R
2Group, R wherein
1Be C
2-C
8Alkyl, comprise straight chain and side chain and cyclic (comprising aryl) alkyl, and C preferably
2-C
4Alkylidene; R
2Be C
1-C
8Alkyl straight chain and side chain and cyclic comprises aryl and hydroxyl alkyl (oxyhydrocarbyl), and C preferably
1-C
4Alkyl, especially methyl or phenyl.Z
2Be polyhydroxy alkyl part (or its oxyalkylated (preferred ethoxylation or propenoxylated) derivant), have at least 2 (under the situation of glyceraldehyde) or at least 3 hydroxyls (under the situation of other reducing sugar) that directly link to each other with chain with linear hydrocarbyl chain.Z
2Preferably come from the reducing sugar in the reductive amination process, Z
2It most preferably is glycidyl (glycityl) part.Suitable reducing sugar comprises glucose, fructose, maltose, lactose, galactose, mannose and xylose, and glyceraldehyde.The corn syrup that high glucose is arranged that can be used as raw material, the corn syrup of high fructose and the corn syrup of high malt sugar and the various sugar of listing above.These corn syrup can obtain Z
2Sugared mixture of ingredients.Should be clear, do not get rid of the meaning of other suitable raw material at this.Z
2Be preferably selected from CH
2(CHOH)
n-CH
2OH, CH (CH
2OH)-(CHOH)
N-1-CH
2OH, CH
2(CHOH)
2(CHOR ') CHOH) CH
2OH, wherein n is the 1-5 integer of (comprising 1 and 5), and R ' is H or cyclic monosaccharide or polysaccharide and alkoxy derivative thereof.As mentioned above, in the most preferred glycidyl, n is 4, especially CH
2-(CHOH)
4-CH
2OH.
Most preferred polyhydroxy fatty acid amide has formula R
8(CO) N (CH
3) CH
2(CHOH)
4CH
2The structure of OH, wherein R
8Be C
6-C
19Straight chained alkyl or alkenyl.In the following formula chemical compound, R
8-CO-N＜can be, for example coconut oleoyl amine, stearmide, oleamide, lauramide, myristamide, decyl amide, caprylamide, palmitamide, Adeps Bovis seu Bubali amide etc.
The exemplary ionic surfactant pack that is applicable to the present composition is drawn together primary amine, for example coco amine (with Adagen 160D (TM) trade name available from Witco) and alkanolamide, for example coconut oleoyl amine MEA is (with Empilan CME (TM) trade name available from Albright ﹠amp; Wilson), the PEG-3 coconut oleoyl amine, coconut oleoyl amine DEA is (with Empilan CDE (TM) available from Albright ﹠amp; Wilson), lauramide MIPA, lauramide MEA is (with Empilan LME (TM) available from Albright ﹠amp; Wilson), lauramide DEA and their mixture.
Be applicable to that amphoteric surfactant of the present invention comprises the ammonium derivative of (a) formula [V]:
R wherein
1Be C
5-C
22Alkyl or alkenyl, R
2Be CH
2CH
2OH or CH
2CO
2M, M are H, alkali metal, alkaline-earth metal, ammonium or alkanol ammonium, and R
3Be CH
2CH
2OH or H;
(b) the amino-alkane hydrochlorate of formula [VI]
R
1NH(CH
2)
nCO
2M
The iminodiacetic alkanoate of formula [VII]
R
1N[(CH
2)
mCO
2M]
2
And the imino group multichain alkyl salt of formula (VIII)
N wherein, m, p and q are the numbers of 1-4, and R
1Be independently selected from group defined above with M; With
(c) their mixture.
(a) the suitable amphoteric surfactant of class comprises the chemical compound of formula V, wherein R
1Be C
8H
17(especially iso-octyl), C
9H
19And C
11H
23Alkyl.(a) the suitable amphoteric surfactant of class have commercially available, commodity Miranol by name and Empigen.
In the CTFA name, be applicable to that material of the present invention comprises cocos nucifera oil both sexes carboxyl propionate, cocos nucifera oil both sexes carboxyl propanoic acid, cocos nucifera oil both sexes acetate, cocos nucifera oil both sexes diacetin (perhaps being called cocos nucifera oil both sexes carboxyl glycinate), lauryl both sexes (lauroampho) sodium acetate (perhaps being called lauryl both sexes carboxyl Glycine sodium).Concrete commodity comprise that trade name is the product (many propylamine of carboxymethyl Adeps Bovis seu Bubali sodium) of Ampholak 7TX, Empigen CDL60 and CDR 60 (Albright﹠amp; Wilson), Miranol H2M Conc.Miranol C2M Conc.N.P., MiranolC2M Conc.O.P., Miranol C2M SF, Miranol CM Special, MiranolUltra L32 and C32 (Rhone-Poulenc); Alkateric 2CIB (AlkarilChemicals); Amphoterge W-2 (Lonza, Inc.); Monateric CDX-38, Monateric CSH-32 (Mona Industries); Rewoteric AM-2C (RewoChemical Group); With Schercotic MS-2 (Scher Chemicals).
Should know have multiple such commercially available amphoteric surfactant all be with for example hydroxide counter ion counterionsl gegenions or with anion sulfate or sulfosalt surfactant, especially sulphation C
8-C
18Alcohol, C
8-C
18The alcohol of ethoxylation or C
8-C
18The electric neutrality complex form preparation of acylglycerol esters and sale.Viewpoint based on mildness and product stability preferably is substantially free of the compositions of (non-ethoxylatedization) sulfated alcohols surfactant.Note also the concentration of amphoteric surfactant and the not form complexed that weight ratio is based on surfactant, any anion surfactant counter ion counterionsl gegenions should be thought the part of whole anion surfactant composition.
(b) that the suitable examples of amphoteric surfactants of class comprises N-alkyl polytrimethylene is poly--, carboxymethyl amine (its commodity Ampholak X07 by name and Ampholak 7CX, sell by Berol Nobel) and the salt of salt, especially triethanolamine salt and N-lauryl-Beta-alanine and N-lauryl-imino group-dipropionic acid.Deriphat that the commodity of this class raw material Henkel by name sells and the Mirataine that sells by Rhone-Poulenc.
Compositions of the present invention also can contain the 0.1%-20% that has an appointment, 0.1%-10% more preferably from about, the zwitterionic surfactant of especially about 1%-8% (weight).
Be applicable to that the water solublity beet alkali surface activator in the present composition comprises formula R
5R
6R
7N ' (CH
2)
nCO
2The amido betaine of the alkyl betaine of M and formula (IX):
R wherein
5Be C
5-C
22Alkyl or alkenyl, R
6And R
7Be C independently
1-C
3Alkyl, M are H, alkali metal, alkaline-earth metal, ammonium or alkanol ammonium, and each number of 1-4 naturally of n, m.Preferred betanin comprises cocamidopropyl propyl-dimethyl carboxymethyl betaine (being sold with Tego betanin trade name by THGoldschmidt) and lauroyl amido propyl-dimethyl carboxymethyl betaine (sold with Empigen BR trade name by Albright and Wilson, sold with Tegobetaine L10S trade name by TH Goldschmidt).
The water solublity sulfobetaines surfactant that is applicable to the present composition comprises the alkylamidoalkyl sulfobetaines of following formula;
R wherein
1Be C
7-C
22Alkyl or alkenyl, R
2And R
3Be C independently
1-C
3Alkyl, M are H, alkali metal, alkaline-earth metal, ammonium or alkanol ammonium, and m and n are the numbers of 1-4.Being applicable to of the present invention is cocamidopropyl propyl hydroxy sulfobetaines, and it is sold with Mirataine CBS trade name by Rhone-Poulenc.
The water-soluble amine oxides surfactant that is applicable to the present composition comprises alkyl amine oxide R
5R
6R
7The amide groups amine oxide of NO and following formula
R wherein
5Be C
11-C
22Alkyl or alkenyl, R
6And R
7Be C independently
1-C
3Alkyl, M are H, alkali metal, alkaline-earth metal, ammonium or alkanol ammonium, and m is the number of 1-4.Preferred amine oxide comprises cocamidopropyl propylamine oxide, lauryl dimethylamine oxide and myristyl dimethylamine oxide.
Suspending agent
The present composition preferably also comprises one or more suspending agents.Be used for suitable suspending agent of the present invention and comprise the acyl derivative of some long-chains or the mixture of this class material.The glycol ester that comprises the fatty acid of about 16-22 carbon atom.Preferred ethylene glycol stearate comprises monostearate and distearate, but especially preferably contains the distearate less than about 7% monostearate.Spendable other suspending agent is to have about 16-22 carbon atom, the alkanolamide of the fatty acid of preferably about 16-18 carbon atom.Preferred alkanolamide is stearic acid monoethanolamide, Stearic acid diethanolamine salt, stearic acid one isopropanol amide and stearic acid monoethanolamide stearate.
Other suitable suspending agent is alkyl (C
16-C
22) dimethyl oxidation amine, for example stearyl dimethyl amine oxide and trihydroxy stearin, the latter is sold with Thixcin (RTM) trade name by Rheox.The Thixcin (RTM) that to be used for preferred suspending agent of the present invention be Rheox.
The content of suspending agent is preferably about 0.1%-5%, more preferably from about 0.1%-3%.Suspending agent can make product have pearlescent gloss in order to help the suspension of water-insoluble oil.Also can use the mixture of suspending agent in the compositions of the present invention.
Optional member
The polymerizing cationically conditioner
Compositions of the present invention can randomly contain the polymerizing cationically conditioner.In compositions of the present invention, the polymerizing cationically conditioner is extremely important, and it is in order to provide ideal dermal sensation.In addition, the polymerizing cationically conditioner combines with water-insoluble oil, might promote the deposition of hydrophobicity skin care actives.If present, the content of polymeric skin conditioning agent is preferably about 0.01%-5%, 0.01%-3% more preferably, especially about 0.01%-2% (weight).
Suitable polymer blend is high molecular weight material (for example the weight average molecular weight by light scattering determining is generally about 2,000-5,000,000, preferred about 5,000-3,000,000, more preferably from about 1 00,000-1,000,000).
The representative types of polymer comprises cationic guar gum, cationic polysaccharide, by acrylic acid and/or deutero-cationic homopolymer of methacrylic acid and copolymer, the cationic cellulose resin, quaternised hydroxyethyl ether cellulose, dimethyl diallyl ammonium chloride and acrylamide and/or acrylic acid cation copolymer, the cationic homopolymer of dimethyl diallyl ammonium chloride, the copolymer of dimethylaminoethyl methacrylate and acrylamide, the copolymer of acrylic acid/dimethyl diallyl ammonium chloride/acrylamide, the quaternized vinyl pyrrolidone acrylate or the methacrylate copolymer of amino alcohol, the quaternized copolymer of vinyl pyrrolidone and dimethyl aminoethyl Methacrylamide, vinyl pyrrolidone/vinyl imidazole methochloride copolymer and polyalkylene and ethyoxyl polyalkyleneimine; Quaternized silicone, the terpolymer of acrylic acid, methacryl amido oxypropyl trimethyl ammonium chloride and acrylic acid methyl ester.; And their mixture.
For example, be applicable to that cationic polymer of the present invention comprises cationic guar gum, as Hydroxyproyl Trimethyl ammonium guar gum (substitution value (d.s.) is 0.11-0.22) (commodity are called JaguarC-14-S (RTM), Jaguar C-17 (RTM) and Jaguar C-16 (RTM)), it also contains hydroxypropyl substituent group (substitution value is 0.8-1.1) except that containing the above-mentioned cation group of pointing out; (commodity are called Ucare PolymerJR-30M, JR-400, LR400, Catanal (RTM) and Celquat) with quaternised hydroxyethyl ether cellulose.Other suitable cationic polymer is the homopolymer (trade name Merquat 100) of dimethyl diallyl ammonium chloride, the copolymer of dimethyl amino ethyl methacrylate and acrylamide, the copolymer of dimethyl diallyl ammonium chloride and acrylamide (trade name Merquat 550 and Merquat S), acrylic acid/dimethyl diallyl ammonium chloride/acrylamide copolymer (trade name Merquat 3330), acrylic acid, the terpolymer of methacryl amido oxypropyl trimethyl ammonium chloride and acrylic acid methyl ester. (trade name Merquat 2001), the quaternized vinyl pyrrolidone acrylate of amino alcohol or methacrylate copolymer (trade name Gafquat), for example polyquaternary ammonium salt 11,23 and 28 (the quaternized copolymer-Gafquat 755N of vinyl pyrrolidone and dimethylaminoethyl methacrylate and the quaternized copolymer of vinyl pyrrolidone and dimethyl aminoethyl Methacrylamide-HS-100), vinyl pyrrolidone/vinyl imidazole methochloride copolymer (trade name Luviquat FC370) polyquaternary ammonium salt 2 and polyalkyleneimine, for example polyethylene imine based and ethoxylation polyethylene imine based.Be applicable to that other polymer of the present invention is with the commercially available cationic polymer of Aqualon N-Hance trade name.
Compositions of the present invention also can contain the 0.1%-20% that has an appointment, preferably about 1%-15%, the more preferably from about oily deutero-non-ionic surface active agent of 2%-10% (weight) or the mixture of oily deutero-non-ionic surface active agent.In compositions of the present invention, oily deutero-non-ionic surface active agent when using and the dermal sensation beneficial effect after using play an important role.Be used for suitable oily deutero-ionic surfactant pack of the present invention draw together water solublity, by the emollient that animals and plants obtain, the triglyceride that for example has polyglycol chain to insert; The monoglyceride of ethoxylation and diester, the butter derivant of many ethoxylations lanoline and ethoxylation.Be used for the preferred oily deutero-non-ionic surface active agent of a class of the present invention and have the structure of general formula (XII):
Wherein n is about 5-200, preferably about 20-100, and 30-85 more preferably from about, and wherein R comprises average about 5-20 carbon atom, the aliphatic group of preferably about 7-18 carbon atom.
The oils and fats of the ethoxylation that this class is suitable comprises glyceryl cocoate, caproin, caprylin, tallow acid glyceride, tripalmitin, tristerin, glyceryl laurate ester, olein, castor oil acid glyceride, and by triglyceride derived fatty acid glyceride, for example Petiolus Trachycarpi oil, almond oil and Semen Maydis oil, the polyethyleneglycol derivative of preferred tallow acid glyceride and glyceryl cocoate.
Such suitable oily deutero-non-ionic surface active agent is can be available from the Croda Inc. (U.S., the commodity of Crovol series New York), Crovol EP40 (PEG 20 Radix Oenotherae erythrosepalae glyceride) for example, Crovol EP 70 (PEG 60 Radix Oenotherae erythrosepalae glyceride), Crovol A-40 (PEG20 Semen Armeniacae Amarum glyceride), Crovol A-70 (PEG 60 Semen Armeniacae Amarum glyceride), Crovol M-40 (PEG 20 corn glyceride), Crovol M-70 (PEG 60 corn glyceride), CrovolPK-40 (PEG 12 palm kernel glyceride) and Crovol PK-70 (PEG 45 palm kernel glyceride) and can be available from the Solan series of products of Westbrook Lanolin, Solan E for example, the lanoline of E50 and the many ethoxylations of X and Aqualose L-20 (PEG 24 lanolin alcohols) and Aqualose W15 (PEG 15 lanolin alcohols).The suitable surfactant of such other is can be available from Sherex Chemical Co. (Dublin, Ohio, Varonic LI series of surfactants USA) and can be available from the Rewoderm series of surfactants of Rewo.These comprise, for example, Varonic LI 48 (Polyethylene Glycol (n=80) tallow acid glyceride, perhaps be called PEG 80 tallow acid glyceride), Varonic LI 2 (PEG 28 tallow acid glyceride), Varonic LI 420 (PEG 200 tallow acid glyceride), with Varonic Ll 63 and 67 (PEG30 and PEG 80 glyceryl cocoate), Rewoderm LI5-20 (PEG-200 cetylate), Rewoderm LIS-80 (PEG-200 cetylate and PEG-7 glyceryl cocoate) and Rewoderm LIS-75 (PEG-200 cetylate and PEG-7 glyceryl cocoate) and their mixture.The PEG derivant that other the oily deutero-emollient that is suitable for is Semen Maydis oil, American Avocado Tree oil and babassu oil, and Softigen 767 (PEG (6) caprylic/capric glyceride).
Be applicable to non-ionic surface active agent and the derivant thereof that also has by the mixed plant adipose-derived of from Shea Tree (Butyrospermum KarkiiKotschy), extracting of the present invention.The plant fat of these the known Shea of being called Butter in non-ly be widely used in various fields, for example soapmaking and as blocking frost, it is sold by Sederma (78610 Le Perray EnYvelines, France).Particularly suitable is the ethoxylated derivative of Shea Butter, it is can be available from Karlshamn Chemical Co. (Columbos, Ohio, USA) Lipex series chemical products, for example Lipex 102 E-75 and Lipex 102 E-3 (one and two glyceride of the ethoxylation of Sheabutter) and can be available from the Croda Inc. (U.S., New York) Crovol series chemical products, for example Crovol SB-70 (one, two glyceride of the ethoxylation of Shea butter).Equally, the ethoxylated derivative of Fructus Mangifera Indicae, cocoa and East India Sapotaceae vegetable butter also can be used in the compositions of the present invention.Though these are classified as ethoxylated non-ionic surface active agent, should know the vegetable oil or the fat that also can have a certain proportion of non-ethoxylatedization.
Other suitable oily deutero-ionic surfactant pack is drawn together the ethoxylated derivative of following oil: almond oil, Oleum Arachidis hypogaeae semen, Testa oryzae oil, Semen Tritici aestivi germ oil, Semen Lini oil, simmondsia oil, Apricot kernel oil, Oleum Juglandis, palm kernel oil, pistachio nut oil, Oleum sesami, rapeseed oil, cade oil, Semen Maydis oil, Semen Persicae oil, seed of Papaver somniferum L. powder, Oleum Pini, Oleum Ricini, soybean oil, American Avocado Tree oil, safflower oil, Oleum Cocois, hazelnut oil, olive oil, Oleum Vitis viniferae and sunflower seed oil.
Based on best mildness and dermal sensation, the deutero-non-ionic surface active agent of highly preferred oil is Lipex 102-3 (RTM) (the PEG-3 ethoxylated derivative of Shea Butter) and Softigen 767 (RTM) (PEG-6 caprylic/capric glyceride).
Compositions of the present invention also can contain the lipophilic emulsifier as other skin care actives.Suitable lipophile skin care actives comprises the anion emulsifier of food grade, and described emulsifying agent comprises and the monoglyceride blended diacid of succinylated monoglycerides, citric acid monostearate, diacetyl tartaric acid glyceryl monostearate and composition thereof for example.
Except above-mentioned water-insoluble poly ﹠ Alpha ,-olefin oil, other water-insoluble oil also can be used in the compositions of the present invention.Other water-insoluble oil that is used for personal cleaning compositions of the present invention is the branched alkyl of following formula or (b) class oil of alkenyl material:
R wherein
1Be H or C
1-C
4Alkyl, R
4Be C
1-C
4Alkyl, R
2Be H or C
1-C
4Alkyl or C
2-C
4Alkenyl, and R
3Be H or C
1-C
4Alkyl or C
2-C
4Alkenyl, n are the integers of 0-3, and m is the integer of 1-1000, have about 600-1000, preferably about 750-1000, the number-average molecular weight of especially about 800-1000.Under 40 ℃, adopt ASTM D-445 viscosity measurement, branched alkyl or alkenyl class oil preferably have about 500cst to about 50,000cst, preferably about 1000cst is extremely about 10, the viscosity of 000cst.
Suitable alkyl or the alkenyl material that is used for (b) of the present invention class is the polymer of butylene, isoprene, terpenes, styrene or isobutene., the polymer of preferred butylene or isobutene..
(b) example of class alkyl or alkene base oil comprises polybutene oil, for example can be available from the product of the commodity of Amoco Indopol 40 by name and Indopol 100; Polyisobutylene oil for example can be available from the product of the commodity of Presperse Inc. Permethyl 104A by name with available from the Parapol 950 of ExxonChemicals Co..
Being used for other suitable material of the present invention has the hydrophobic modified silicone of following formula:
Wherein R is C
1-C
4Alkyl or phenyl, R ' are C
1-C
20Alkyl or phenyl, z are 5-21, and x is the number that meansigma methods is about 20-400, and y is that meansigma methods is about the number of 0-10 and x+y in the 30-400 scope.The x value of preferred material is 40-200, preferred 60-100, the y value is 0-5, preferred 0 and x and y value sum be 60-100.Alkylidene chain z can be a straight or branched.In addition, the branch branching structure that the silicone skeleton can have a low degree with form resin (as, MDQ or MDT resin).
The example of this class oil comprises can be available from the commodity of GE Silicones SF1632 (C by name
16-C
18The alkyl methyl silicone) hydrophobic modified silicone, and octyl group and decyl methyl silicone.
In preferred embodiments, the number average particle diameter of other water-insoluble oil is about 1 micron-500 microns, preferably about 5-200 micron, 5-50 micron more preferably from about, especially about 5-20 micron.
Another kind is applicable to that the water-insoluble skin/hair-care composition of composition, foam of the present invention is the polyol carboxylate of liquid.
Being preferred for polyol ester of the present invention is polyol carboxylate non-plugging liquid or liquable.These polyol esters are derived with one or more carboxylic acid groups or part by polyhydroxy group or part.In other words, these esters comprise part and the one or more part by carboxylic acid derivatives by polyol derivative.These carboxylates also can be by carboxylic acid derivatives.These carboxylates can also be described as the liquid polyol fatty acid ester, because term carboxylic acid and fatty acid often exchange use in the art.
Be used for preferred liquid polyol polyester of the present invention and comprise some polyhydric alcohol, especially sugar or the sugar alcohol of using at least four fatty acid-based esterifications.Therefore, but the polyhydric alcohol raw material must have the hydroxyl of at least four esterifications.The example of preferred polyhydric alcohols is a sugar, comprises monosaccharide and disaccharide and sugar alcohol.The example that contains the monosaccharide of four hydroxyls is xylose and arabinose, and is xylitol (having five hydroxyls) by the deutero-sugar alcohol of xylose.The monosaccharide erythrose is not suitable for the present invention, because it only contains three hydroxyls, but by the deutero-sugar alcohol of erythrose, promptly erythritol contains four hydroxyls, thereby can use.The suitable monosaccharide that contains five hydroxyls is galactose, fructose and sorbose.Hydrolyzate and glucose and the deutero-sugar alcohol that contains six hydroxyls of sorbose by sucrose also suit as Sorbitol.Spendable disaccharide examples of polyhydric alcohols comprises maltose, lactose and sucrose, and they all have 8 hydroxyls.
The preferred polyol that is used to prepare the polyester that the present invention uses is selected from erythritol, xylitol, Sorbitol, dextrose plus saccharose.Especially preferably sucrose.
At least four hydroxyls with polyhydric alcohol raw material of at least four hydroxyls are contained the fatty acid esterification of about 8-22 carbon atom.That the example of this class fatty acid comprises is sad, capric acid, lauric acid, myristic acid, myristoleic acid, Palmic acid, palmitoleic acid, stearic acid, oleic acid, castor oil acid, linoleic acid, linolenic acid, eleostearic acid, arachidic acid, arachidonic acid, behenic acid, erucic acid.Fatty acid can derive from natural or synthetic fatty acid; They can be saturated or unsaturated, comprise position and geometric isomer.Yet, being preferred for liquid polyester of the present invention for providing, the fatty acid at least about 50% weight that enters in the polyester molecule should be undersaturated.Particularly preferably be oleic acid and linoleic acid and their mixture.
Be used for polyol fatty acid polyesters of the present invention and should comprise at least four fatty acid ester groups.All hydroxyls of polyhydric alcohol needn't be all by fatty acid esterification, but polyester preferably contains two nonesterified hydroxyls at the most.Most preferably all basically hydroxyls of polyhydric alcohol are all by fatty acid esterification, and promptly polyol moiety is complete esterification basically.The fatty acid of esterification in the polyhydric alcohol molecule can identical or form of mixtures, but as mentioned above, must exist a considerable amount of unsaturated acids ester groups to provide mobile.
In order to set forth above-mentioned viewpoint, the sucrose tri-fatty acid ester is not suitable for the present invention, because it does not contain four required fatty acid ester groups.Sucrose four fatty acid esters suit, but are not preferred, because it has more than two nonesterified hydroxyls.Sucrose six fatty acid esters are preferred, are no more than two nonesterified hydroxyl because it has.It is highly preferred that wherein all hydroxyls comprise the fatty acid ester of sucrose eight replacements of liquid all by fatty acid-esterified chemical compound.
Following is to be applicable to the limiting examples that contains the concrete polyol fatty acid polyesters of at least four fatty acid ester groups of the present invention: glucose four oleates, glucose four soya fatty acids (undersaturated) ester, mannose four mixing soya beans fatty acid oil esters, galactose four oleates, arabinose four linoleates, xylose four linoleates, galactose five oleates, sorbitol four oleates, sorbitol six unsaturated soya fatty acid esters, xylitol five oleates, sucrose four oleates, sucrose five oleates, sucrose six oleates, sucrose seven oleates, sucrose eight oleates and their mixture.
As implied above, highly preferred polyol fatty acid ester is that wherein fatty acid contains those of about 14-18 carbon atom.
The complete fusing point that is used for preferred liquid polyol polyester of the present invention is lower than about 30 ℃, preferably is lower than about 27.5 ℃, more preferably less than about 25 ℃.The complete fusing point of this paper is measured by differential scanning calorimetry (DSC).
Be applicable to that polyol fatty acid polyesters of the present invention can pass through the known prepared in various methods of those of ordinary skills.These methods comprise: adopt various catalyst, with the polyol ester exchange process of fatty acid methyl ester, ethyl ester or glyceride; Method with fat acyl chloride acidylate polyhydric alcohol; Method with fatty acid anhydride acidylate polyhydric alcohol; With with the method for fatty acid acidylate polyhydric alcohol etc.Referring to United States Patent (USP) 2,831,854; The United States Patent (USP) 4,005,196 of Jandacek (mandate on January 25th, 1977).
The present composition can also comprise that auxiliary nonionic or anionic property polymerization thickening component, especially molecular weight are greater than about 20,000 water-soluble polymer." water-soluble polymer " be meant under 25 ℃, can form the material of substantial transparent solution and the viscosity that this material can increase water during 1% concentration in water.Example as the ideal water-soluble polymer of the additional thickening component of the present composition is hydroxyethyl-cellulose, hydroxypropyl cellulose, hydroxypropyl methylcellulose, Polyethylene Glycol, polyacrylamide, polyacrylic acid, polyvinyl alcohol (example comprises the PVA 217 of Japanese KuraryChemical Co.), polyvinylpyrrolidone K-120, glucosan (for example can be available from D﹠amp; The pure product 2P of the Dextran of O Chemiicals), carboxymethyl cellulose, plant exudate (as arabic gum, ghatti gum and Tragacanth), seaweed extract (as sodium alginate, propylene glycol alginate and carrageenin sodium).Preferred substance as additional thickener of the present invention is a natural polysaccharide.The example of this class material is guar gum, locust bean gum and xanthan gum.Be applicable to that other preferred substance of the present invention is that molecular weight is about 700,000 hydroxyethyl-cellulose.
Hydrotropic agent
One of compositions of the present invention optionally feature be to contain hydrotropic agent.Be applicable to that hydrotropic agent of the present invention is well known in the art, comprise sodium xylene sulfonate, ammonium xylene sulfonate, cumene sodium sulfonate, short-chain alkyl sulfate and composition thereof.Hydrotropic content can be about 0.01%-5% in the present composition, preferably about 0.1%-4%, more preferably from about 0.5%-3% (weight).That the hydrotropic agent of this paper definition is meant is undiluted when being added to, in water soluble surfactant active's system the time, the material of scalable system viscosity and rheological characteristic.
Except that above-mentioned water-insoluble oil, compositions of the present invention also can comprise about at the most 10%, the insoluble spice of preferably about at the most 3% (weight) or soothing oil (cosmetic oil) or wax or their mixture, wherein described oil or wax are insoluble in product substrate under 25 ℃.
Be used for suitable insoluble soothing oil of the present invention and wax and can be selected from the water-insoluble silicone, comprise silicone, the rigidity of nonvolatile poly-alkyl and poly-aryl siloxanes glue and fluid, volatile cyclic polydimethylsiloxane, polyalkoxylated silicone, amino and quaternary ammonium modification crosslinked with strengthen silicone and their mixture, C
8-C
30The C of fatty acid
1-C
24Ester (as isopropyl myristate, myristic acid Semen Myristicae alcohol ester and castor oil acid cetyl), benzoic C
8-C
30Ester, Cera Flava, saturated and undersaturated aliphatic alcohol (as docosanol), hydrocarbon is (as mineral oil, vaseline, squalane and Squalene), the Isosorbide Dinitrate of fatty acid (referring to the US-A-3988255 of Seiden, on October 26th, 1976 issued), lanoline and class oil lanolin derivative, the triglyceride of animal and plant (almond oil for example, Oleum Arachidis hypogaeae semen, Semen Tritici aestivi germ oil, Testa oryzae oil, Semen Lini oil, simmondsia oil, Apricot kernel oil, Oleum Juglandis, palm-kernel oil, pistachio nut oil, Oleum sesami, rapeseed oil, cade oil, Semen Maydis oil, Semen Persicae oil, seed of Papaver somniferum L. powder, Oleum Pini, Oleum Ricini, soybean oil, American Avocado Tree oil, safflower oil, Oleum Cocois, hazelnut oil, olive oil, Oleum Vitis viniferae and sunflower seed oil) and the C of dimerization and trimer acid
1-C
24Ester, for example dimeric dibasic acid diisopropyl ester, two iso stearyl malates, dimeric dibasic acid two iso stearyl esters and trimer acid three different stearyl esters.
The viscosity of final composition (Brookfield DV II, with Cone CP41 or CP52,25 ℃, pure) is preferably at least about 500cps, and more preferably from about 1,000-50,000cps, especially about 1,000-30,000cps, more preferably from about 1,000-15,000cps.
Cleasing compositions of the present invention can randomly comprise other hair or the skin moisturizer that is dissolved in the Cleasing compositions substrate.The preferred content of this class wetting agent is about 0.5%-20% (weight).In preferred embodiments, wetting agent is selected from natural primary amino acid chemical compound and non-occlusive polyhydric alcohol of water solublity (nonpolyol nonocclusive) and their mixture that is present in the keratodermatitis.
Some examples of preferred non-occlusive wetting agent are squalanes, pyrrolidone sodium carboxylate, D-panthenol, lactic acid, the L-proline, guanidine, ketopyrrolidine, aminosal and the deutero-protein of other collagen, Aloe vulgaris glue, acetamide MEA and lactamide MEA and their mixture.
Compositions of the present invention also can comprise opacifier or pearling agent.The content of this class material can be about 0.01%-5%, preferably about 0.1%-1.3% (weight).
Opacifier/the pearling agent that is applicable to the present composition comprises: titanium dioxide, TiO
2EUPERLAN 810 (RTM); TEGO-PEARL (RTM); Long-chain (C
16-C
22) acyl derivative, for example having the glycol or the macrogol ester of the fatty acid of about 16-22 carbon atom, it has 7 inferior ethoxyl unit at the most; Has about 16-22 carbon atom, the alkanolamide of the fatty acid of preferably about 16-18 carbon atom, for example stearic acid monoethanolamide, Stearic acid diethanolamine salt, stearic acid one isopropanol amide and stearic acid monoethanolamide and alkyl (C
16-C
22) dimethylamine oxide stearyl dimethylamine oxide for example.
In preferred compositions, opacifier/pearling agent exists with crystal form.In highly preferred compositions, opacifier/pearling agent is that particle diameter is about 0.05 micron-0.45 micron, preferred about 0.17 micron-0.3 micron graininess polystyrene dispersions considers that from best rheology and shear thinning performance are provided this class dispersion is preferred.It is highly preferred that styrene-acrylate copolymer and the OPACFIER 680 (RTM) that sells by Morton International.
Various other optional, materials can be added in the Cleasing compositions with about 0.1%-2% (weight) content separately.This class material comprises protein and polypeptide and their derivant; Water solublity or water lyotropy antiseptic, DMDM Hydantoin for example, Germall 115, the methyl ester of hydroxy benzoic acid, ethyl ester, propyl ester and butyl ester, EDTA, Euxyl (RTM) K400, natural antiseptic agent is benzylalcohol, potassium sorbate and bisabolol for example; Sodium benzoate and 2-phenyl phenol; Other humidizer, for example hyaluronic acid, chitin and starch-grafted sodium polyacrylate are as can be available from CelaneseSuperabsorbent Materials (Portsmith, VA, USA) and be recorded in US-A-4, Sanwet (RTM) IM-1000, IM-1500 and the IM-2500 in 076,663; Solvent; Low temperature phase modifier for example ammonium ion source (as NH
4Cl); Viscosity-control additive such as magnesium sulfate and other electrolyte; Coloring agent; TiO
2And TiO
2The Muscovitum of-coating; Spice and spice solubilizing agent; And zeolite such as Valfour BV400 and derivant and Ca
2+/ Mg
2+Chelating agen such as multi-carboxylate (or salt), amino multi-carboxylate (or salt), polyphosphonate (or salt), aminopolyphosphonic acid ester (or salt), EDTA etc., water softener such as sodium citrate and insoluble granule be zinc stearate and pyrogenic silica for example.The content of water preferably accounts for about 20%-99.89% of present composition weight, and preferably about 40%-90% is more preferably at least about 75%.
The pH of compositions is preferably about 3-10,5-9 more preferably from about, especially about 5-8, most preferably from about 5-7.
Compositions of the present invention can be used in various skins and the hair-care application, for example bath gels, body lotion, shampoo etc.
Compositions of the present invention can with hands use or preferably with implement for personal cleaning for example foams (puff) use.The suitable implement for personal cleaning that is used for the present composition comprises following patent literature those disclosed, these documents are incorporated by reference at this paper: the US-A-5 of Campagnoli, 144,744 (JIUYUE was authorized on the 8th in 1992), the US-A-3 of Barnhouse, 343,196, the WO95/26671 of P﹠G, the WO95/00116 of P﹠G and the WO95/26670 of P﹠G.
Compositions of the present invention is illustrated by following non-limiting examples.
Example I-III is a bath lotion composition.EXAMPLE IV and V are shampoo composites.
| I/％ | II/％ | III/％ | IV/％ | V/％ | |
| Lauryl ether-3 ammonium sulfate (Empicol EAC/TP) 1 | 8.4 | 8.4 | 10.5 | 15 | 15 |
| Ammonium lauryl sulfate (Empicol AL30) 1 | - | - | - | 5 | 5 |
| Lauryl both sexes sodium acetate (Empigen CDL60P) 1 | 3.6 | 3.6 | 4.5 | - | 2 |
| Sodium lauroyl sarcosine (Hamposyl L30) 2 | 0.5 | 0.5 | 3 | - | - |
| Cocamidopropyl MEA (Empilan CME) 1 | - | - | - | 1.0 | 1.0 |
| Spermol | - | - | - | 0.4 | 0.4 |
| Stearyl alcohol | - | - | - | 0.2 | 0.2 |
| Glycol distearate | - | - | - | 2.0 | 2.0 |
| Thixcin R 3 | 1.5 | 1.5 | 0.3 | - | - |
| Poly alpha olefin (Puresyn 100) 4 | 6.0 | 0 | 3.0 | 4.0 | 0 |
| Poly alpha olefin (Puresyn 40) 4 | 0 | 5 | 0 | 0 | 2 |
| Spice | 0.5 | 0.5 | 1.0 | 1.0 | 1.0 |
| EDTA | 0.11 | 0.11 | 0.11 | 0.11 | 0.11 |
| Sodium benzoate | 0.25 | 0.25 | 0.25 | 0.25 | 0.25 |
| DMDM Hydantoin | 0.138 | 0.138 | 0.138 | 0.138 | 0.138 |
| NaCl | 0.5 | 0.5 | 1.3 | 0.5 | 0.5 |
| Neko | 0.15 | 0.0 | 0.0 | 0.15 | 0.15 |
| Octyl methoxycinnamate | 0.0 | 2.1 | 0.0 | 0.0 | 0.0 |
| Vitamin e acetate | 0.0 | 0.0 | 0.2 | 0.0 | 0.0 |
| Citric acid | 0.9 | 0.9 | 0.9 | 0.4 | 0.4 |
| Water | Add to 100 | ||||
Example VI is a body lotion.
| VI(％) | |
| Lauryl ether-3 ammonium sulfate (Empicol EAC/TP) 1 | 9 |
| Ammonium xylene sulfonate (AXS) 1 | 0-1.66 |
| The alkylsurfuric acid ammonium | 5 |
| Zinc stearate | 1.0 |
| Sodium dihydrogen phosphate | 0-0.6 |
| Sodium hydrogen phosphate | 0-0.6 |
| Spermol | 0.4 |
| Stearyl alcohol | 0.2 |
| Macrogol 600 | 1.4 |
| Polybutene | 0.1-1.2 |
| Spice | 0.6 |
| The EDTA disodium | 0.1 |
| Coconut monoethanol amide (CMEA) 1 | 1.0 |
| Glycol distearate (EGDS) | 2.0 |
| NaCl | 0-2 |
| Kathon CG | 0.02 |
| Neko | 0.15 |
| Triclosan | 0.25 |
| Water | Add to 100 |
1. supplier: Albright ﹠amp; Wilson UK Limited, P.O.Box 15, Whitehaven, Cumbria, CA28 9QQ
2. supplier: Hampshire Chemicals, Corp., 55 Hayden Ave., Lexington, MA 02173, USA
3. supplier: Rheox, Inc., Wyckoffs Mill Road, P.O.Box 700, Hightstown, NJ 08520, USA
4. supplier: Mobil Chemical Company, P.O.Box 3140, Edison, New Jersey, 08818-3140, USA
Manufacture method
Compositions can prepare by the pre-composition that at first prepares part surface activating agent, suspending agent and thickening agent.This pre-composition contains surfactant and all the lauryl both sexes acetates that account for compositions gross weight 50-70%.By under gentle agitation, surfactant (except that sarcosinate), part water, powder antiseptic and pH regulator agent are mixed with pre-composition.Then this mixture heated is arrived about 90 ℃, stir adding suspending agent down during this period.
Make this mixture after high temperature keeps several minutes, use heat exchanger to control its cooldown rate, thereby suspending agent is crystallized out.
In this pre-composition, add remaining water, add remaining surfactant, antiseptic, spice, sodium chloride and hydrophobicity skin care activity component then.For some hydrophobicity skin care activity component, need high shear mixing.At last, add water-insoluble oil.This part technology at room temperature adopts gentle stirring to carry out, to obtain the preferred drop that mean diameter is the 5-20 micron.
This product has good rheological properties in storage, distribution and use, the good deposition of skin care activity composition is provided, and have good cleaning sensation and mildness and favorable effects, comprise skin condition, skin moisture-keeping, good stable, cleaning and foaminess.
Claims (15)
1. the liquid personal cleansing composition that can wash off, contain:
(a) water;
(b) water soluble surfactant active of 1 weight %-60 weight %;
(c) water-insoluble oil is selected from the following highly branched poly alpha olefin of general formula,
R wherein
1Be H or C
1-C
20Alkyl, R
4Be C
1-C
20Alkyl, R
2Be H or C
1-C
20Alkyl, R
3Be C
3-C
20Alkyl, n are the integer of 0-3 and the integer that m is 1-1000, have the number-average molecular weight of 1000-25000, and described personal cleaning compositions is under 40 ℃, and when measuring viscosity with ASTM D-445 method, the water-insoluble oil viscosity is 300-50,000 centistoke; With
(d) hydrophobicity skin care activity composition is selected from antimicrobial, sunscreen, vitamin, aromatic oil, anthelmintic, antifungal and their mixture, and wherein the ClogP value of hydrophobicity skin care activity composition is greater than 3,
Described compositions does not contain the soap class.
2. the personal cleaning compositions of claim 1, wherein the ClogP value of hydrophobicity skin care activity composition is greater than 5.
3. claim 1 or 2 personal cleaning compositions, wherein hydrophobicity skin care activity composition is an antimicrobial.
4. the personal cleaning compositions of claim 3, wherein antimicrobial is selected from diphenylcarbamide, hexachlorophene, 3,4,5-tribromsalan and their mixture.
5. claim 1 or 2 personal cleaning compositions, wherein antimicrobial is a neko.
6. claim 1 or 2 personal cleaning compositions contain the hydrophobicity skin care activity composition of 0.1%-5% weight.
7. claim 1 or 2 personal cleaning compositions, wherein the number-average molecular weight of water-insoluble oil is 2500-6000.
8. claim 1 or 2 personal cleaning compositions contain the water-insoluble oil of 0.1%-10% weight.
9. claim 1 or 2 personal cleaning compositions, wherein the water soluble surfactant active is selected from anion surfactant, nonionic, amphion and amphoteric surfactant and their mixture.
10. the personal cleaning compositions of claim 9, wherein water soluble anionic surfactant is selected from alkyl sulfate; the alkyl sulfate of ethoxylation; alkyl glyceryl ether sulfonate; the alkyl ethoxy glycerol ether sulfonate; acyl methyl taurine salt; fat acidyl glycine salt; alkyl ethoxy carboxylate; the N-acyl glutamate; acyl isethinate; alkyl sulfo succinate; the alkyl ethoxy sulfosuccinate; α-alpha-sulfonated fatty acid; α-alpha-sulfonated fatty hydrochlorate; α-sulfonated fatty acid ester; alkyl phosphate; the alkyl phosphate of ethoxylation; acyl sarcosinates and fatty acid/protein condensation substance; acylaspartic acid salt; alkoxyl amido-carboxylic acid salt; the alkanolamide sulfosuccinate of ethoxylation; the alkyl citric acid sulfosuccinate of ethoxylation; the acyl group ethylene diamine triacetate; acyl group ethoxy isethionate; amide groups alcoxyl base sulfate; linear alkylbenzene sulfonate (LAS); paraffin sulfonate; alkyl alkoxy sulfate and their mixture.
11. the personal cleaning compositions of claim 9, wherein water soluble anionic surfactant is the alkyl sulfate of ethoxylation.
12. the personal cleaning compositions of claim 10, wherein the soluble amphoteric surfactant is selected from the ammonium derivative of formula [V]:
R wherein
1Be C
5-C
22Alkyl or alkenyl, R
2Be CH
2CH
2OH or CH
2CO
2M, M are H, alkali metal, alkaline-earth metal, ammonium or alkanol ammonium, and R
3Be CH
2CH
2OH or H.
13. the personal cleaning compositions of claim 10, wherein zwitterionic surfactant is selected from formula R
5R
6R
7N
+(CH
2)
nCO
2The amido betaine of the alkyl betaine of M and formula (IX):
R wherein
5Be C
5-C
22Alkyl or alkenyl, R
6And R
7Be C independently
1-C
3Alkyl, M are H, alkali metal, alkaline-earth metal, ammonium or alkanol ammonium, and each integer of 1-4 naturally of n, m.
14. the compositions of claim 1 or 2, the cationic polymerization skin conditioning agent that also contains 0.01%-5% weight, they are selected from cationic guar gum, cationic polysaccharide, by acrylic acid and/or deutero-cationic homopolymer of methacrylic acid and copolymer, the cationic cellulose resin, quaternised hydroxyethyl ether cellulose, dimethyl diallyl ammonium chloride and acrylamide and/or acrylic acid cation copolymer, the cationic homopolymer of dimethyl diallyl ammonium chloride, the copolymer of dimethylaminoethyl methacrylate and acrylamide, the copolymer of acrylic acid/dimethyl diallyl ammonium chloride/acrylamide, the quaternized vinyl pyrrolidone acrylate or the methacrylate copolymer of amino alcohol, the quaternized copolymer of vinyl pyrrolidone and dimethyl aminoethyl Methacrylamide, vinyl pyrrolidone/vinyl imidazole methochloride copolymer and polyalkylene and ethyoxyl polyalkyleneimine, quaternized silicone, acrylic acid, the terpolymer of methacryl amido oxypropyl trimethyl ammonium chloride and acrylic acid methyl ester., and their mixture.
15. the personal cleaning compositions of claim 1 or 2, wherein the number average bead diameter of water-insoluble oil is 1 micron-500 microns.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| USPCT/US99/01515 | 1999-01-25 | ||
| WOPCT/US99/01515 | 1999-01-25 | ||
| PCT/US1999/001515 WO2000042984A1 (en) | 1999-01-25 | 1999-01-25 | Cleansing compositions |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN1341012A CN1341012A (en) | 2002-03-20 |
| CN1203840C true CN1203840C (en) | 2005-06-01 |
Family
ID=22272044
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CNB008042462A Expired - Fee Related CN1203840C (en) | 1999-01-25 | 2000-01-20 | Cleaning compositions |
Country Status (8)
| Country | Link |
|---|---|
| EP (1) | EP1156779A1 (en) |
| JP (1) | JP2003521466A (en) |
| KR (1) | KR100501784B1 (en) |
| CN (1) | CN1203840C (en) |
| AU (2) | AU2469099A (en) |
| CA (1) | CA2359481A1 (en) |
| CZ (1) | CZ20012650A3 (en) |
| WO (2) | WO2000042984A1 (en) |
Families Citing this family (26)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20030092586A1 (en) * | 2001-09-06 | 2003-05-15 | Colgate-Palmolive Company | Composition |
| AU2003213604A1 (en) * | 2002-03-19 | 2003-10-08 | The Procter And Gamble Company | Liquid personal cleansing compositions containing acyl sarcosinates |
| GT200500050A (en) * | 2004-03-16 | 2005-10-24 | PESTICIDE COMPOSITIONS FOR SEED TREATMENT | |
| AU2005247397A1 (en) * | 2004-05-18 | 2005-12-08 | Cockerell Dermatology Development, Ltd. | Syndet bars having ultraviolet radiation protection |
| KR100591793B1 (en) | 2005-02-16 | 2006-06-26 | 씨제이라이온 주식회사 | Powdered cleanser composition for scrub effect |
| JP2007077029A (en) * | 2005-09-12 | 2007-03-29 | Kao Corp | Aqueous hair washing agent |
| KR100792040B1 (en) * | 2006-11-01 | 2008-01-04 | 하인숙 | Cleansing soap |
| JP5285230B2 (en) * | 2007-04-11 | 2013-09-11 | 花王株式会社 | Disinfectant cleaning composition |
| KR100845393B1 (en) * | 2007-05-03 | 2008-07-09 | 애경산업(주) | A conditioning shampoo composition |
| US8623343B2 (en) | 2007-07-17 | 2014-01-07 | Basf Se | Highly cationic copolymers based on quaternized nitrogen-containing monomers |
| KR101687033B1 (en) * | 2008-06-19 | 2016-12-15 | 디에스엠 아이피 어셋츠 비.브이. | Shampoo preparations |
| JP2011524883A (en) * | 2008-06-19 | 2011-09-08 | ディーエスエム アイピー アセッツ ビー．ブイ． | Shampoo formulation |
| EP2916814B1 (en) | 2012-11-06 | 2020-02-12 | Colabs International Corporation | Composition containing a cellulose derived capsule with a sunscreen |
| US11491088B2 (en) | 2012-11-06 | 2022-11-08 | CoLabs International Corporation | Compositions containing a capsule with a moisturizing agent |
| US10322301B2 (en) | 2012-11-06 | 2019-06-18 | CoLabs International Corporation | Compositions containing a cellulose derived capsule with a sunscreen active agent |
| US11724134B2 (en) | 2012-11-06 | 2023-08-15 | CoLabs International Corporation | Compositions containing a cellulose derived capsule with a sunscreen active agent |
| US11707421B2 (en) | 2012-11-06 | 2023-07-25 | Colabs Int'l Corp. | Compositions containing a flexible derived capsule with an active agent |
| US11690793B2 (en) | 2012-11-06 | 2023-07-04 | Colabs Int'l Corp. | Composition containing a cellulose derived capsule with a sunscreen |
| US9861565B2 (en) | 2012-12-04 | 2018-01-09 | Colgate-Palmolive Company | Cleansing composition |
| JP6270622B2 (en) * | 2014-05-20 | 2018-01-31 | 日華化学株式会社 | Antibacterial and antifungal agent for textile and method for producing antibacterial and antifungal fiber product |
| JP6490000B2 (en) * | 2015-11-27 | 2019-03-27 | 花王株式会社 | Skin cleanser composition |
| PL3775134T3 (en) * | 2018-04-04 | 2022-10-31 | Dow Global Technologies, Llc | Aqueous cleaning formulation |
| AU2019291885A1 (en) | 2018-06-27 | 2021-02-04 | CoLabs International Corporation | Compositions comprising silicon dioxide-based particles including one or more agents |
| US20220117859A1 (en) * | 2018-11-30 | 2022-04-21 | 3M Innovative Properties Company | Topical antimicrobial microemulsions with fluorescent materials |
| CN110923718B (en) * | 2019-12-12 | 2022-05-06 | 广东红日星实业有限公司 | Water-soluble fine polishing solution and preparation method thereof |
| CN115251049B (en) * | 2022-07-29 | 2024-07-23 | 浙江工业大学 | Pesticide solubilizing carrier and preparation method and application thereof |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2705891B1 (en) * | 1993-06-01 | 1995-08-18 | Oreal | Cosmetic compositions containing at least one anionic surfactant of the alkylgalactoside uronate type and at least one synthetic hydrocarbon oil and their uses for the treatment of keratin materials. |
| WO1996018383A1 (en) * | 1994-12-15 | 1996-06-20 | Albemarle Corporation | Stable water-in-synthetic hydrocarbon fluid emulsions |
| US6008173A (en) * | 1995-11-03 | 1999-12-28 | Colgate-Palmolive Co. | Bar composition comprising petrolatum |
| JP2000515563A (en) * | 1998-06-04 | 2000-11-21 | ザ、プロクター、エンド、ギャンブル、カンパニー | Hair conditioning composition containing poly-α-olefin oil |
-
1999
- 1999-01-25 AU AU24690/99A patent/AU2469099A/en not_active Abandoned
- 1999-01-25 WO PCT/US1999/001515 patent/WO2000042984A1/en active Application Filing
-
2000
- 2000-01-20 WO PCT/US2000/001390 patent/WO2000042985A1/en active IP Right Grant
- 2000-01-20 AU AU28539/00A patent/AU771123B2/en not_active Ceased
- 2000-01-20 CZ CZ20012650A patent/CZ20012650A3/en unknown
- 2000-01-20 CN CNB008042462A patent/CN1203840C/en not_active Expired - Fee Related
- 2000-01-20 JP JP2000594442A patent/JP2003521466A/en active Pending
- 2000-01-20 EP EP00906965A patent/EP1156779A1/en not_active Withdrawn
- 2000-01-20 KR KR10-2001-7009350A patent/KR100501784B1/en not_active IP Right Cessation
- 2000-01-20 CA CA002359481A patent/CA2359481A1/en not_active Abandoned
Also Published As
| Publication number | Publication date |
|---|---|
| CN1341012A (en) | 2002-03-20 |
| AU2469099A (en) | 2000-08-07 |
| KR20010102994A (en) | 2001-11-17 |
| JP2003521466A (en) | 2003-07-15 |
| WO2000042984A1 (en) | 2000-07-27 |
| AU2853900A (en) | 2000-08-07 |
| KR100501784B1 (en) | 2005-07-18 |
| WO2000042985A1 (en) | 2000-07-27 |
| CZ20012650A3 (en) | 2002-01-16 |
| AU771123B2 (en) | 2004-03-11 |
| EP1156779A1 (en) | 2001-11-28 |
| CA2359481A1 (en) | 2000-07-27 |
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