TW201109035A - Composition - Google Patents
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- TW201109035A TW201109035A TW99116697A TW99116697A TW201109035A TW 201109035 A TW201109035 A TW 201109035A TW 99116697 A TW99116697 A TW 99116697A TW 99116697 A TW99116697 A TW 99116697A TW 201109035 A TW201109035 A TW 201109035A
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- 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
- A61Q5/12—Preparations containing hair conditioners
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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
- A61K8/31—Hydrocarbons
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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
- A61K8/42—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
- A61K8/46—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
- A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
- A61K8/84—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions otherwise than those involving only carbon-carbon unsaturated bonds
- A61K8/89—Polysiloxanes
- A61K8/891—Polysiloxanes saturated, e.g. dimethicone, phenyl trimethicone, C24-C28 methicone or stearyl dimethicone
- A61K8/892—Polysiloxanes saturated, e.g. dimethicone, phenyl trimethicone, C24-C28 methicone or stearyl dimethicone modified by a hydroxy group, e.g. dimethiconol
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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
- A61K8/92—Oils, fats or waxes; Derivatives thereof, e.g. hydrogenation products thereof
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- 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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- Dermatology (AREA)
- Cosmetics (AREA)
Abstract
Description
201109035 六、發明說明: 【發明所屬之技術領域】 油之叙合物 本發明係關於一種包括甘油三酸酯 【先前技術】 二酸酯油之經改 儘管有先前技術,然而仍需要包括甘油 良濃縮調理洗髮精組合物。 【發明内容】 因此,本發明提供根據申請專利範圍技 _叫永項1之濃縮調 理洗髮精組合物。 根據本發明組合物提供濃縮洗髮精經改良的濕潤調理觸 感。此尤其令人驚舒的是因為局表面活性劑會容易產生沙 沙聲及較為雜亂的感覺。 甘油三酸酯油 合適之甘油三酸S旨油包括脂肪及油(包括天然脂肪及 油),諸如:荷荷芭油、大豆油、葵花籽油、米糠油、鱷 梨樹(avocado)油、杏仁油、撖欖油、芝麻油、藏麻油、椰 子油、椰子樹油、向日葵油、紹油;可可脂;牛油、豬 油’·前述油經氫化作用後所得之硬化油;及合成甘油單、 二及三酸酯(諸如,肉豆蔻酸甘油酯及2_乙基己酸甘油 酯)。 較佳地,甘油三酸酯油係以該組合物重量計為〇 〇5至1〇 重量。/。存在’尤其是0.2至5重量%,特別是〇.5至3重量%。 烴油 合適之烴油具有至少12個碳原子’且包括石壤油、聚稀 148372.doc 201109035 煙油、礦物油、飽和及不飽和十二烷、飽和及不飽和十三 烷、飽和及不飽和十四烷、飽和及不飽和十五烷、飽和及 不飽和十六烷、及其混合物。亦可採用該等化合物之具支 鏈異構體’以及高碳數鏈長度之煙^匚2_6稀基單體之聚合 烴(諸如聚異丁烯)亦是合適的。 亦可採用任何以上該等油之混合物。 較佳地,10至100重量%之烴油具有於3〇t下根據ASTM D-445測得之0.01至60〇 cPs之黏度。 0 較佳地,該煙油係以該組合物重量計為〇 〇5至1 〇重量% 存在,尤其是0.2至5重量%,且特別是0.5至3重量%。 酯油 用於本發明組合物中之其他組分為酯油。該酯油可賦予 洗髮精調理效益。 合適之酯油具有至少1〇個碳原子,且包括帶有衍生自脂 肪酸或醇之烴基鏈的g旨。一般的g旨油為化學式R,C〇〇R, ◎ 其中R'及R獨立地表示烷基或烯基,且R,及R中碳原子總計 為至少10個’較佳至少20個。亦可採用羧酸之二·及三烧 基及烯基酷。 亦可採用任何以上該等油之混合物。 較佳地’酯油係以該組合物重量計為至丨〇重量%存 在,尤其是0.2至5重量%,且特別是〇_5至3重量〇/0。 聚α浠煙油 合適之聚α烯烴油包括該等衍生自丨_伸烷基單體(具有6 至16個碳,較佳為6至12個碳)之油。這些材料之非限制性 148372.doc 201109035 貫例包括1-己烯、1-辛稀、卜癸烯、卜十二烯、卜十四 烯、1-十六烯、分支化異構體(諸如4_甲基小戊烯)及其混 合物。經氫化聚癸烯為另一種合適之材料。 曰較佳之聚α稀烴油包括購_obil公司之具有約5〇〇之數 里平均分子量之商標名為Puresyn 6、具有約3嶋之分子量 之Puresyn 1〇〇及具有約6000之分子量之puresyn 3〇〇之聚癸 稀。 較佳地,聚《烯烴油係以該組合物重量計為〇 〇5至1〇重 量%存在’尤其是0.2至5重量% ’且特別是〇⑴重量%。 調理凝膠相 該調理凝膠網絡包括: (a) 脂肪物質; 其包含具有16至30個 (b) 凝膠網絡陰離子表面活性劑 碳之烷基; (c)陽離子表面活性劑; 其中該調理凝膠網絡整體不帶電荷或為陰離子性。 該陽離子表面活性劑提供脂肪物f/陰離子表面活性劑 凝膠網絡經改良的穩固性而使同樣包括非陽離子清潔相之 組合物產生改良的調理效益。該清潔相中陰離子表面活性 劑及調理凝膠中之陰離子表面活性劑間碳鍵長度之差異會 善該調理凝膠網絡的安定性,並維持其在洗髮精組 合物中的完整性。 較佳地,該凝膠網絡巾之㈣子及陽離子表面活,㈣之 碳鏈長度差包含4個以内之碳數目,較佳為糊碳原子^ 148372.doc 201109035 佳者係兩活性劑含相同數量的碳。 更佳地,彼者係包含碳赫 長度差在4個以内的單一烷基,更 紙 文仏者2個以内,而最佳者θ 相同的長度。此可幫助維持凝膠網絡的安定性。 疋 較佳地,該凝膠網絡陽離子表面活性财的碳係存在於 单-烷基中。更佳地,該凝膠網絡陽離子表面活性 16至30個碳。 ,、有 該調理凝膠網絡係在將組合物剩餘組分併入之前製造。 該油可在包併入至洗髮精之前分散於調理凝膠相^或 後來添加。 ~ GN陽離子表面活性劑 較佳地,該調理凝膠網絡包括具有14至3〇個碳之陽離子 表面活性劑。 較佳地,该凝膠網絡陽離子表面活性劑中的碳係存在於 單一烷基中。更佳地,該凝膠網絡陽離子表面活性劑具有 16至3 0個碳。 Q 較佳地’該陽離子表面活性劑具有化學式 Ν»(Ι12)(Ι13)(Ιΐν 其中 Ri、R2、R3 及 R4係獨立地為于(Ci6 至C3Q)烷基或苄基。 較佳地,R1、R2、R3及R4其中之一、其中之二或其中之 二係獨立地為(C至C3〇)烧基’而其餘R1、R2、R3及R4美 團或該等基團則為烷基或苄基。 烧基可視需要在烧基鍵内可包含一或多個 或-COO-)及/或醚(-0-)鍵。烷基可視情況經—或多個經基 取代。烷基可為直鏈或具支鏈,及環狀(當具有3個或多個 148372.doc 201109035 碳原子之烷基時)。該烷基可為飽和或可包含一或多個碳_ 碳雙鍵(例如油基)。烷基視需要在該烷基鏈上經一或多個 伸乙基氧基進行乙氧基化。 用於根據本發明調理劑組合物之合適的陽離子表面活性 劑包括氯化十六烧基三甲銨、氣化二十二院基三甲錄、氯 化十六烧基吼啶鏽、氯化四甲銨、氯化四乙銨、十八烷基 一甲基苄基氯化銨、氯化椰油基基三甲銨、pEG_2_油基氯 化銨及其對應之氫氧化物。其他合適的陽離子表面活性劑 包括CTFA名稱為四級敍鹽(Quaternium)_5、四級敍鹽!及 四級銨鹽-1 8之彼等物質。任何前述物質之混合物亦合201109035 VI. Description of the invention: [Technical field to which the invention pertains] The present invention relates to a triglyceride containing a triglyceride. [Prior Art] Diester oil has been modified, although it has prior art, it still needs to include glycerin. Concentrated conditioning shampoo composition. SUMMARY OF THE INVENTION Accordingly, the present invention provides a concentrated conditioning shampoo composition according to the scope of the patent application. The compositions according to the present invention provide improved moisturizing conditioning feel for concentrated shampoos. This is especially surprising because local surfactants are prone to rustling and a messy sensation. Triglyceride oils Suitable triglycerides S oils include fats and oils (including natural fats and oils) such as jojoba oil, soybean oil, sunflower oil, rice bran oil, avocado oil, Almond oil, eucalyptus oil, sesame oil, sesame oil, coconut oil, coconut tree oil, sunflower oil, oil; cocoa butter; butter, lard' · hardened oil obtained by hydrogenation of the aforementioned oil; and synthetic glycerin , di- and tri-acid esters (such as glyceryl myristate and 2-ethylhexanoic acid). Preferably, the triglyceride oil is from 5 to 1 weight by weight of the composition. /. There is, in particular, 0.2 to 5% by weight, in particular 〇. 5 to 3% by weight. Suitable hydrocarbon oils for hydrocarbon oils have at least 12 carbon atoms' and include rocky oil, poly 148372.doc 201109035 smoky oil, mineral oil, saturated and unsaturated dodecane, saturated and unsaturated tridecane, saturated and not Saturated tetradecane, saturated and unsaturated pentadecane, saturated and unsaturated hexadecane, and mixtures thereof. It is also suitable to use a branched hydrocarbon isomer of these compounds and a polymeric hydrocarbon such as polyisobutylene having a high carbon number chain length. Mixtures of any of the above may also be employed. Preferably, from 10 to 100% by weight of the hydrocarbon oil has a viscosity of from 0.01 to 60 〇 cPs as measured according to ASTM D-445 at 3 Torr. Preferably, the smoky oil is present in an amount of from 5 to 1% by weight, based on the weight of the composition, especially from 0.2 to 5% by weight, and especially from 0.5 to 3% by weight. Ester Oil The other component used in the compositions of the present invention is an ester oil. The ester oil imparts conditioning benefits to the shampoo. Suitable ester oils have at least one carbon atom and include a hydrocarbyl chain derived from a fatty acid or an alcohol. The general g oil is a chemical formula R, C〇〇R, ◎ wherein R' and R independently represent an alkyl group or an alkenyl group, and the total number of carbon atoms in R and R is at least 10', preferably at least 20. It is also possible to use a carboxylic acid di- and a tri-alkyl group and an alkenyl group. Mixtures of any of the above may also be employed. Preferably, the ester oil is present in an amount of up to 5% by weight, based on the weight of the composition, especially from 0.2 to 5% by weight, and especially from 〇5 to 3 parts by weight/0. Polyalphaphthalene oleum Suitable polyalphaolefin oils include those derived from oxime alkylene monomers having from 6 to 16 carbons, preferably from 6 to 12 carbons. Non-limiting examples of these materials 148372.doc 201109035 Examples include 1-hexene, 1-octyl, decimene, dodecene, tetradecene, 1-hexadecene, branched isomers (such as 4-methylpentene) and mixtures thereof. Hydrogenated polydecene is another suitable material. Preferably, the poly-α-lean hydrocarbon oil comprises a pure molecular weight of about 5 之 in the _obil company under the trade name Puresyn 6, a puresyn 1 具有 having a molecular weight of about 3 〇〇, and a puresyn having a molecular weight of about 6,000. 3 〇〇 癸 。 。 。. Preferably, the poly"olefin oil is present in an amount of from 5 to 1% by weight, based on the weight of the composition, especially '0.2 to 5% by weight' and especially 〇(1)% by weight. Conditioning gel phase The conditioning gel network comprises: (a) a fatty material; comprising an alkyl group having 16 to 30 (b) gel network anionic surfactant carbon; (c) a cationic surfactant; wherein the conditioning The gel network as a whole is uncharged or anionic. The cationic surfactant provides improved stability of the fat f/anionic surfactant gel network to result in improved conditioning benefits for compositions that also include a non-cationic cleansing phase. The difference in carbon bond length between the anionic surfactant in the cleansing phase and the anionic surfactant in the conditioning gel will improve the stability of the gel network and maintain its integrity in the shampoo composition. Preferably, the (4) and cationic surface of the gel network towel are active, and the carbon chain length difference of (4) comprises 4 carbon atoms, preferably a paste carbon atom ^ 148372.doc 201109035 preferably the two active agents contain the same The amount of carbon. More preferably, the other comprises a single alkyl group having a carbon-tooth length difference of 4 or less, and more than 2 paper lengths, and the best θ is the same length. This can help maintain the stability of the gel network. Preferably, the carbon network of the gel network cationic surface active is present in the mono-alkyl group. More preferably, the gel network has a cationic surface activity of from 16 to 30 carbons. The conditioning gel network is made prior to incorporation of the remaining components of the composition. The oil can be dispersed in the conditioning gel phase or added later before the package is incorporated into the shampoo. ~ GN Cationic Surfactant Preferably, the conditioning gel network comprises a cationic surfactant having 14 to 3 carbons. Preferably, the carbon system in the gel network cationic surfactant is present in a single alkyl group. More preferably, the gel network cationic surfactant has from 16 to 30 carbons. Q Preferably, the cationic surfactant has the formula Ν»(Ι12)(Ι13) (Ιΐν where Ri, R2, R3 and R4 are independently (Ci6 to C3Q) alkyl or benzyl. Preferably, One of R1, R2, R3 and R4, two or two of which are independently (C to C3〇)alkyl groups and the remaining R1, R2, R3 and R4 groups or such groups are alkane The base or the benzyl group may optionally contain one or more or -COO-) and/or ether (-0-) bonds in the base bond. The alkyl group may optionally be substituted with one or more via groups. The alkyl group may be straight or branched, and cyclic (when having three or more alkyl groups of 148372.doc 201109035 carbon atoms). The alkyl group can be saturated or can contain one or more carbon-carbon double bonds (eg, an oil base). The alkyl group is optionally ethoxylated on the alkyl chain via one or more extended ethyloxy groups. Suitable cationic surfactants for use in the conditioner compositions according to the present invention include hexadecyltrimethylammonium chloride, gasification of twenty-two yards of trimethyl sulphate, hexadecanoyl decyl rust, and chlorinated tetramethyl chloride. Ammonium, tetraethylammonium chloride, octadecyl-methylbenzylammonium chloride, chlorinated trimethylammonium chloride, pEG_2_oleyl ammonium chloride and its corresponding hydroxide. Other suitable cationic surfactants include those under the CTFA name Quaternium _5, quaternary salt salt, and quaternary ammonium salt -18. a mixture of any of the foregoing substances
適。種特別適用於根據本發明調理劑之陽離子表面活性 劑為例如可購自Hoechst Celanese公司之GENAMiN CTAC 商品之氣化十六烷基三甲銨。另一種特別適用於根據本發 明調理劑之陽離子表面活性劑為例如可購自公司 之GENAMIN KDMP商品之氯化二十二烷基三甲銨。 另一類適用於本發明之陽性離子表面活性劑實例(單獨 使用或併與一或多種其他陽離子調理表面活性劑混合)為 下列⑴及(ii)之組合: (i)對應於以下通式⑴之醯胺基胺: /R2suitable. Cationic surfactants which are particularly suitable for use in the conditioning agent according to the present invention are, for example, gasified cetyltrimethylammonium commercially available from the GENAMi N CTAC product of Hoechst Celanese. Another cationic surfactant which is particularly suitable for use in conditioners according to the present invention is, for example, behenyl chloride, commercially available from the company, GENAMIN KDMP. Another example of a positive ionic surfactant suitable for use in the present invention (alone or in combination with one or more other cationic conditioning surfactants) is a combination of the following (1) and (ii): (i) corresponding to the following general formula (1) Amidoxime: /R2
R^ONHCCHj^N \r3 其中R係為具有1 〇個或更多個碳原子之烴基鏈, R2及R3獨立地選自1至10個碳原子之烴基鏈且 148372.doc 201109035 m為1至約ι〇之整數;及 (ii)酸。 文中所採用之用語烴基鏈意指烷基鏈或烯基鏈。 較佳之酿胺基胺化合物為該等對應於化學式⑴之化合 物’其中:R1為具有約11至約24個碳原子之烴基,R2及R3 各自獨立地為具有1至約4個碳原子之烴基(較佳為烷基), 且m為1至約4之整數。 較佳地’ R2及R3為曱基或乙基。 較佳地,m為2或3,亦即伸乙基或伸丙基。 適用於文中之較佳醢胺基胺包括硬脂醢胺基丙基二甲 胺、硬脂醯胺基丙基二乙胺、硬脂醯胺基乙基二乙胺、硬 脂醯胺基乙基二甲胺、棕橺醯胺基丙基二甲胺、棕櫚醯胺 基丙基二乙胺、棕櫚醯胺基乙基二乙胺、棕櫚醯胺基乙基 二曱胺、山嵛醯胺基丙基二曱胺、山嵛醯胺基丙基二乙 胺、山嵛醯胺基乙基二乙胺、山嵛醯胺基乙基二甲胺、花 生四烯醯胺基丙基二曱胺、花生四烯醯胺基丙基二乙胺、 花生四烯醯胺基乙基二乙胺、花生四烯醯胺基乙基二甲 胺、及其混合物。 適用於本文之尤佳醯胺基胺為硬脂醯胺基丙基二甲胺、 硬脂醯胺基乙基二乙胺、及其混合物。R^ONHCCHj^N \r3 wherein R is a hydrocarbyl chain having 1 or more carbon atoms, and R2 and R3 are independently selected from a hydrocarbyl chain of 1 to 10 carbon atoms and 148372.doc 201109035 m is 1 to An integer of about ι〇; and (ii) an acid. The term hydrocarbyl chain as used herein means an alkyl chain or an alkenyl chain. Preferred amine amino amine compounds are those corresponding to the formula (1) wherein R1 is a hydrocarbon group having from about 11 to about 24 carbon atoms, and R2 and R3 are each independently a hydrocarbon group having from 1 to about 4 carbon atoms. (preferably an alkyl group), and m is an integer from 1 to about 4. Preferably, 'R2 and R3 are anthracenyl or ethyl. Preferably, m is 2 or 3, i.e., an extended or extended propyl group. Preferred guanamine amines suitable for use herein include stearyl propyl dimethyl dimethylamine, stearyl propyl propyl diethylamine, stearyl amide ethyl diethyl amide, stearyl amide Dimethylamine, palmitoylpropyl dimethylamine, palmitosylpropyldiethylamine, palmitosylethyldiethylamine, palmitoylethyldiamine, behenamide Propyldiamine, behenylpropyldiethylamine, behenylethyldiethylamine, behenylethyl dimethylamine, arachidonic acid propylidene Amine, arachidonic acid propyldiethylamine, arachidonic acid ethyl diethylamine, arachidonic acid ethyl dimethylamine, and mixtures thereof. Suitable guanamine amines for use herein are stearyl propyl dimethyl dimethylamine, stearyl amidoethyl diethylamine, and mixtures thereof.
適用於本文商業上購得之醢胺基胺包括:以商標名 LEXAMINE S-13 購自 Inolex(Philadelphia Pennsylvania, USA)及以商標名 AMIDOAMINE MSP 購自 Nikko(Tokyo, Japan)之硬脂醯胺基丙基二曱胺、以商標名AMIDOAMINE 148372.doc 201109035 S購自Nikko之硬脂醯胺基乙基二乙胺、以商標名 INCROMINE BB購自 Croda(North Humberside, England)之 山嵛醯胺基丙基二甲胺、及以商標名SCHERCODINE系列 購自 Scher(Clifton New Jersey,USA)之各種醯胺基胺。 酸(ii)是為可將護髮組合物中之醯胺基胺進行質子化之 任一有機酸或礦物酸。適用於本文之合適的酸包括氳氯 酸、醋酸、酒石酸、富馬酸、乳酸、馬來酸、琥珀酸、及 其混合物。較佳地,該酸選自由醋酸、酒石酸、氫氣酸、 富馬酸、及其混合物組成之群。 該酸的主要作用係將護髮組合物中之酿胺基胺進行質子 化’因此可在该§蒦髮組合物中及位形成三級胺鹽 (tertiary amine salt ; TAS)。該TAS在功效上為一種非永久 性四級銨或假四級銨陽離子表面活性劑。 合適地,所包含的酸係為使所有所存在之醯胺基胺進行 質子化之足夠含量,亦即至少與組合物中所存在之醯胺基 胺量含量係相等莫耳之量。 陽離子表面活性劑之含量範圍以該組合物總重量為基礎 之陽離子表面活性劑總重量計為〇 〇1至1〇重量%,更佳地 為0.02至7.5重量%,最佳地為〇 〇5至5重量0/〇。 GN脂肪物質 本發明組合物之調理凝膠網絡較佳包括脂肪物質。 較佳地,該脂肪物質係選自脂肪酸、脂肪酸醯胺、脂肪 族醇、脂肪酸酯及其混合物。 較佳地,該脂肪物質包括具有14至3〇個碳原子之脂肪 H8372.doc 1Λ 201109035 族,更佳者為16至22個碳原子。合適脂肪族醇之實例包括 十六烷醇、十八炫醇及纟混合&。合適脂月方酸醋之一實例 為甘油單硬脂酸酯。 本發明組合物中脂肪物質的含量以該組合物重量計合適 地為0·01至1 〇重量%,較佳為〇〗至5重量%。 較佳地,脂肪物質及凝膠網絡陰離子表面活性劑間之比Commercially available guanamine amines are commercially available from Inolex (Philadelphia Pennsylvania, USA) under the tradename LEXAMINE S-13 and from the stearylamine base of Nikko (Tokyo, Japan) under the trade name AMIDOAMINE MSP. Propyldiamine, commercially available from Nikko's stearylamine ethyldiethylamine under the trade name AMIDOAMINE 148372.doc 201109035 S, available from Croda (North Humberside, England) under the trade name INCROMINE BB. Propyl dimethylamine, and various guanamine amines available from Scher (Clifton New Jersey, USA) under the trade name SCHERCODINE series. The acid (ii) is any organic or mineral acid which can protonate the guanamine amine in the hair care composition. Suitable acids suitable for use herein include chloric acid, acetic acid, tartaric acid, fumaric acid, lactic acid, maleic acid, succinic acid, and mixtures thereof. Preferably, the acid is selected from the group consisting of acetic acid, tartaric acid, hydrogen acid, fumaric acid, and mixtures thereof. The primary function of the acid is to protonate the amine amine in the hair care composition' thus forming a tertiary amine salt (TAS) in place in the § hair composition. The TAS is functionally a non-permanent quaternary ammonium or pseudo quaternary ammonium cationic surfactant. Suitably, the acid is included in an amount sufficient to protonate all of the guanamine amine present, i.e., at least in an amount equivalent to the amount of guanamine present in the composition. The cationic surfactant is present in an amount ranging from 〇〇1 to 1% by weight, more preferably from 0.02 to 7.5% by weight, most preferably 〇〇5, based on the total weight of the cationic surfactant. Up to 5 weights 0/〇. GN Fatty Material The conditioning gel network of the compositions of the present invention preferably comprises a fatty material. Preferably, the fatty material is selected from the group consisting of fatty acids, fatty acid guanamines, fatty alcohols, fatty acid esters, and mixtures thereof. Preferably, the fatty material comprises a fat having from 14 to 3 carbon atoms, H8372.doc 1Λ201109035, more preferably 16 to 22 carbon atoms. Examples of suitable aliphatic alcohols include cetyl alcohol, octadecyl alcohol, and hydrazine blends & An example of a suitable fatty acid vinegar is glyceryl monostearate. The content of the fatty substance in the composition of the present invention is suitably from 0.01 to 1% by weight, preferably from 〇 to 5% by weight, based on the weight of the composition. Preferably, the ratio between the fatty substance and the gel network anionic surfactant
例為〇·1:1至亂·卜較佳地為m50:I,更佳地為ΐ 5:ι 至1 〇: 1及最佳地為約2:1。 較佳地,該凝膠網絡之陰離子及脂肪物質包含具有4個 以内,較佳2個碳及最佳相同碳數之烷基。更佳地,彼者 包含4個以内、更佳2個以内及相同長度為最佳之單烷基。 此可幫助維持凝膠網絡的穩定性。 GN陰離子表面活性劑 本發明組合物之調理凝膠相較佳包括凝膠網絡陰離子表 面活性劑。 Ο 肖陰離子表面活性劑包含具有16至3G個碳之絲鏈,較 佳地為16至22個碳。 較佳地,該凝膠網絡陰離子表面活性劑中之碳係存在於 單一烧基中。 該凝膠網絡包括陰離子表面活性劑,以達到該凝膠網絡 整體上帶陰離子電荷,或使該凝膠網絡整體上不帶電荷。 δ亥凝膠網絡陰離子表面活性劑係以該組合物重量計為 0.1至5重量%存在,且更佳地為〇5至2〇重量%。 清潔相 148372.doc 201109035 该清潔相包括清潔用表面活性劑。該清潔相陰離子表面 活性劑具有8至14個碳原子,更佳地為Mu個及最佳地 為12個碳原子。更佳地’該等碳係存在於單-院基中。 較佳之陰離子清潔用表面活性劑包括驗金屬燒基硫酸 鹽’更佳地炫基醚硫酸醋。尤佳之陰離子清潔用表面活性 劑包括月桂基驗硫酸納。 省:月潔相包括以該組合物重量計之27至7〇重量。清潔用 表面活性劑,較佳地為35至5〇重量%。 陽離子沈積聚合物 根據本發明組合物包括陽離子沈 在一較佳之實施例中 積聚合物。 口、之陽離子沈積輔助聚合物可為經陽離子取代或從兩 或夕種單體形成之均聚物。聚合物之重量平均(I)分子量 -般介於⑽_及2 _ _道爾頓(dah〇n)之間。該等聚 合物可具有陽離子含象其 3虱基團,諸如四級銨或質子化胺基、 或其混合物。若聚合物的分子量太低,則調理效果差。若 :二則可能在傾倒組合物時,㈣高延展性黏度導致組 &物絲黏性之問題。 a陽離子含乳基團—般係作為陽離子聚合物總單體單元 :::分上之取代基。因此’當該聚合物不為均聚物時, ^可匕含間隔物非陽離子單 早體早几。泫專聚合物描述於第 A化妝品成分指導τρ Δ广 . n. V (CTFA Cosmetic IngredientFor example, 〇·1:1 to chaos·b is preferably m50:I, more preferably ΐ5:ι to 1 〇: 1 and most preferably about 2:1. Preferably, the anionic and fatty materials of the gel network comprise an alkyl group having 4 or less, preferably 2 carbons, and most preferably the same carbon number. More preferably, the other comprises a monoalkyl group of 4 or less, more preferably 2 or less, and the same length. This can help maintain the stability of the gel network. GN Anionic Surfactant The conditioned gel phase of the compositions of the present invention preferably comprises a gel network anionic surfactant. The Ο-anionic surfactant comprises a chain of filaments having from 16 to 3G carbons, preferably from 16 to 22 carbons. Preferably, the carbon network in the gel network anionic surfactant is present in a single alkyl group. The gel network includes an anionic surfactant to achieve an anionic charge throughout the gel network or to render the gel network as a whole uncharged. The alpha gel network anionic surfactant is present in an amount of from 0.1 to 5% by weight, based on the weight of the composition, and more preferably from 5 to 2% by weight. Cleansing phase 148372.doc 201109035 This cleansing phase includes cleaning surfactants. The cleansing phase anionic surfactant has from 8 to 14 carbon atoms, more preferably from 10 and most preferably from 12 carbon atoms. More preferably, the carbon systems are present in a single-hospital base. Preferred anionic cleaning surfactants include metal sulphate sulfates, more preferably thioether sulfate vinegar. A particularly good anionic cleaning surfactant includes sodium lauryl sulfate. Province: Moon phase comprises 27 to 7 weights by weight of the composition. The cleaning surfactant is preferably 35 to 5 % by weight. Cationic Deposition Polymer The composition according to the invention comprises a cation which is polymerized in a preferred embodiment. The cation-deposited auxiliary polymer of the mouth may be a homopolymer which is substituted by a cation or formed from a monomer of the two or the ethic. The weight average (I) molecular weight of the polymer is generally between (10) _ and 2 _ _ Dalton (dah〇n). The polymers may have a cationic containing group such as a quaternary ammonium or protonated amine group, or a mixture thereof. If the molecular weight of the polymer is too low, the conditioning effect is poor. If: two may be in the pouring of the composition, (four) high ductility viscosity leads to the problem of group & a cation-containing milk group is generally used as a cationic monomer unit monomer::: a substituent. Thus, when the polymer is not a homopolymer, it can be a few times earlier than the spacer non-cationic precursor.泫Special polymer is described in Section A Cosmetic Ingredient Guide τρ Δ广. n. V (CTFA Cosmetic Ingredient
Directory)中。選擇陽離 %離子早體早兀的比例, 于,子電荷密度在所要求範圍内(一般為〇·2至3.〇 148372.doc 12 201109035 meq/gm)之聚合物。聚合物之陽離子電荷密度可經由美國 藥典(US Pharmacopoeia)所描述之基耶達測氮法(Kjeldahl method)於氮測定化學測試條件下適當地測確定。 例如’合適之陽離子聚合物包括具有陽離子胺之乙烯基 單體之共聚物或具有水溶性間隔物單體之四級銨官能基, 諸如(甲基)丙烯醯胺、烷基及二烷基(甲基)丙烯醯胺、(甲 基)丙烯酸烧基酯、乙烯基己内酯及乙烯基吡咯啶。經烧 q 基及二院基取代之單體較佳具有C1-C7烷基,更佳為C1-3 院基。其他合適之間隔物包括乙烯基酯、乙烯基醇、馬來 酸酐、丙二醇及乙二醇。 該陽離子胺可為一級、二級或三級胺,取決於組合物的 特定種類及pH。一般’二級及三級胺(特定是三級胺)為較 佳者。 經胺取代之乙烯基單體及胺可經聚合作用呈胺形式,且 然後藉由四級銨化作用轉化成銨。 〇 該陽離子聚合物可包括衍生自經胺及/或四級銨取代之 單體及/或相容性間隔物單體之單體單元的混合物。 合適之陽離子聚合物包括,例如: -含陽離子二烯丙基四級銨之聚合物,其包括例如氯化 二曱基二烯丙基銨均聚物及在工業(CTFA)中分別稱為 聚四級銨鹽6及聚四級銨鹽7之丙烯醯胺及氣化二曱基 二烯丙基銨之共聚物; -不飽和羧酸(具有3至5個碳原子)之胺基烷基酯礦物酸 鹽之均聚物及共聚物(描述於U.S.專利4,009,256中); 148372.doc -13- 201109035 -陽離子聚丙制胺消述於而95/22311中)。 可採用之其他陽離子聚合物包括陽離子多醣聚合物,諸 如陽離子纖維素何生物、陽離子澱粉衍生物、及陽離子瓜 爾勝衍生物。 適用於本發明組合物之陽離子多聽聚合物包括以下化學 式之單體: A-0-[R-N+(R1)(R2)(r3)X-j , 其中:A為葡萄糖殘基,諸如澱粉或纖維f葡萄糖殘基。 R為伸烷基、氧基伸烷基、聚氧基伸烷基、或羥基伸烷 ,、或其組合。Rl、R2及R3獨立地表示院基、芳基、烧基 芳基芳基烷基、烷氧基烷基、或烷氧基芳基,每一基團 包含可咼達約1 8個碳原子。每一陽離子部分之碳原子總數 (亦即R、R及R3中碳原子之總數)較佳為約或更少,及 X為陰離子抗衡離子。 另一類陽離子纖維素包括經與在工業(CTFA)中稱為聚四 級銨鹽24之經月桂基二曱基銨取代之環氧化物反應所得之 羥乙基纖維素之聚合四級銨鹽。該等物質可例如以商標名 聚合物LM-200購自Amerchol公司。 其他合適之陽離子多醣聚合物包括含四級氮纖維素謎 (例如描述於U.S.專利3,962,41 8中)、及醚化纖維素及澱粉 之共聚物(例如描述於U.S.專利3,958,581中)。Directory). The ratio of the cation to the % ionic early aging is selected as the polymer having a subcharge density within the desired range (generally 〇·2 to 3. 〇 148372.doc 12 201109035 meq/gm). The cationic charge density of the polymer can be suitably determined by the Kjeldahl method described by the US Pharmacopoeia under nitrogen test chemical test conditions. For example, 'suitable cationic polymers include copolymers of vinyl monomers having a cationic amine or quaternary ammonium functional groups having a water-soluble spacer monomer such as (meth) acrylamide, alkyl and dialkyl ( Methyl) acrylamide, alkyl (meth) acrylate, vinyl caprolactone and vinyl pyrrolidine. The monomer substituted with a benzyl group and a second group preferably has a C1-C7 alkyl group, more preferably a C1-3 group. Other suitable spacers include vinyl esters, vinyl alcohol, maleic anhydride, propylene glycol, and ethylene glycol. The cationic amine can be a primary, secondary or tertiary amine, depending on the particular species and pH of the composition. Generally, 'secondary and tertiary amines (specifically tertiary amines) are preferred. The amine-substituted vinyl monomer and amine can be polymerized in the form of an amine and then converted to ammonium by quaternization. 〇 The cationic polymer may comprise a mixture of monomer units derived from an amine and/or quaternary ammonium substituted monomer and/or a compatible spacer monomer. Suitable cationic polymers include, for example: - polymers containing cationic diallyl quaternary ammonium, including, for example, dinonyl diallyl ammonium chloride homopolymers and referred to as poly in industrial (CTFA), respectively Copolymer of quaternary ammonium salt 6 and polyquaternary ammonium salt 7 of acrylamide and vaporized dimercaptopropyl ammonium; - aminoalkyl group of unsaturated carboxylic acid (having 3 to 5 carbon atoms) Homopolymers and copolymers of ester mineral acid salts (described in US Patent 4,009,256); 148372.doc -13-201109035 - Cationic polypropylamines are described in 95/22311). Other cationic polymers which may be employed include cationic polysaccharide polymers such as cationic cellulose, biological starch derivatives, and cationic guar derivatives. Cationic poly-audiopolymers suitable for use in the compositions of the present invention include monomers of the formula: A-0-[R-N+(R1)(R2)(r3)Xj wherein: A is a glucose residue such as starch or fiber f glucose residue. R is an alkylene group, an alkyloxyalkylene group, a polyoxyalkylene group, or a hydroxyalkylene group, or a combination thereof. Rl, R2 and R3 independently represent a deutero, aryl, alkylarylalkyl, alkoxyalkyl or alkoxyaryl group, each group containing up to about 18 carbon atoms . The total number of carbon atoms per cationic moiety (i.e., the total number of carbon atoms in R, R and R3) is preferably about or less, and X is an anionic counterion. Another class of cationic celluloses include polymeric quaternary ammonium salts of hydroxyethyl cellulose obtained by reaction with an epoxide substituted with lauryl decyl ammonium in the industrial (CTFA). Such materials are commercially available, for example, from Amerchol under the trade name Polymer LM-200. Other suitable cationic polysaccharide polymers include those containing a quaternary nitrogen cellulose puzzle (e.g., as described in U.S. Patent 3,962,41,8), and a copolymer of etherified cellulose and starch (e.g., as described in U.S. Patent 3,958,581).
可採用一類特別合適之陽離子多醣聚合物為陽離子瓜爾 膠衍生物,諸如瓜爾羥丙基三甲基氣化銨(以該等jaguar 商標系列購自Rhodia)。該等物質之實例為jAGUAR 148372.doc -14- 201109035 C13S、JAGUAR C14、JAGUAR C15及 JAGUAR C17。 可採用任何以上陽離子聚合物之混合物。 陽離子聚合物一般存在於本發明洗髮精之含量範圍以該 、、且σ物總重置為基礎之陽離子聚合物總重量計為〇 〇 1至$ 重里%,較佳為〇·〇5至2重量。/。,更佳為〇 〇7至i 2重量〇/〇。 較L地,本發明護髮組合物為水性,亦即彼者具有水或 水溶液’或係以溶致液晶相(丨丫你叩沁liquid crystalline ◎ Phase)作為彼者主要組分。 合適地,該組合物包括的水以該組合物總重量為基礎之 重量計為10至98重量%,較佳30至95重量0/〇。 根據本發明組合物較佳包括聚矽氧。 尤佳之聚矽氧調理劑為聚矽氧乳液,諸如該等藉由聚矽 氧形成之彼者,諸如聚二有機矽氧烷,具體言之CTFA名 稱為二曱聚矽氧烷(dimethicone)之聚二甲基矽氧烷、CTFA 名稱為二甲聚石夕氧醇(dimethiconol)之具有經基端基之聚二 Ο 曱基矽氧烷、及CTFA名稱為胺基矽油(amodimethic〇ne)之 胺基官能基聚二甲基矽氧烷。 乳液微滴在本發明組合物中一般具有〇 〇丨至2〇微米,更 佳0.2至1 〇微米之Sauter平均滴徑(D3,2)。 用於測定Sauter平均滴徑⑴3,2)之合適的方法係根據雷射 光散射採用儀器(諸如Malvern粒度儀)進行。 用於本發明组合物之合適的聚矽氧乳液可購自聚石夕氧供 應商’諸如Dow Corning及GE Silicones。該等預製聚石夕氧 乳液之用途針對處理容易度及控制聚矽氧粒徑而言是較佳 148372.doc 15 201109035 的。該等預製聚矽氧乳液一般可額外地包括合適之乳化劑 (諸如陰離子或非離子乳化劑、或其混合物),且可藉由諸 如乳液聚合法化學乳化法,或藉由採用高剪切混合器之機 械乳化法製得。一般,具有小於0.15微米之Sauter平均滴 徑(D3,2)之預製聚矽氧乳液稱為微乳液。 合適之預製聚矽氧乳液之實例包括乳液DC2-1766、 DC2-1784、DC-1785、DC-1786、DC-1788及微乳液 DC2-1865 及 DC2-1870,所有皆可購自 Dow Corning。DC7051 為 較佳之聚矽氧。此等皆為二甲聚矽氧醇之乳液/微乳液。 胺基矽油乳液(諸如DC2-8177及DC939)及SME253(購自GE Silicones)亦合適。 其中經已與例如描述於WO 03/094874之聚矽氧乳液微滴 摻合之某特定種類的高分子量表面活性嵌段共聚物之聚矽 氧乳液亦是合適的。在該等物質中,該聚矽氧乳液微滴較 佳係藉由諸如以上描述之彼者之聚二有機矽氧烷形成。一 種較佳形式之表面活性嵌段共聚物係根據以下化學式: H0(CH2CH20)x(CH(CH3)CH20)y(CH2CH20)xH 其中X的平均值為4或更大,及y的平均值為25或更大。 另一種較佳形式之表面活性嵌段共聚物係根據以下化學 式: (HO(CH2CH20)a(CH(CH3)CH20)b)2-N-CH2-CH2-N((OCH2CH(CH3))b (OCH2CH2)aOH)2 其中a的平均值為2或更大,及b的平均值為6或更大。 亦可採用任何以上所述之聚矽氧乳液之混合物。 148372.doc -16 - 201109035 上述聚石夕氧乳液-般存在於本發明組合物之含量範圍以 該組合物總重量為基礎之聚錢總重量計為G._i5重量 %,較佳為0.5至12重量%。 該聚石夕氧較佳係存在〇.5至15重量%,更佳地⑴ %。 之額外成分,以提高效 本發明組合物可視需要包含下述 能及/或消費者可接受度。A particularly suitable class of cationic polysaccharide polymers can be employed as cationic guar gum derivatives, such as guar hydroxypropyltrimethylammonium hydride (available from Rhodia in the series of such jaguar trademarks). Examples of such materials are jAGUAR 148372.doc -14-201109035 C13S, JAGUAR C14, JAGUAR C15 and JAGUAR C17. Mixtures of any of the above cationic polymers may be employed. The cationic polymer is generally present in the range of the shampoo of the present invention in an amount of from 〇〇1 to $% by weight based on the total weight of the cationic polymer based on the total reset of the σ substance, preferably 〇·〇5 to 2 weight. /. More preferably 〇 至 7 to i 2 weight 〇 / 〇. More preferably, the hair care composition of the present invention is aqueous, i.e., the other has water or an aqueous solution' or a liquid crystalline phase (the liquid crystalline phase ◎ Phase) as the main component. Suitably, the composition comprises water in an amount of from 10 to 98% by weight, preferably from 30 to 95% by weight, based on the total weight of the composition. The composition according to the invention preferably comprises polyfluorene oxide. Particularly preferred polyoxymethylene conditioning agents are polyoxynoxy emulsions, such as those formed by polyoxymethylene, such as polydiorganotoxioxane, specifically the CTFA name is dimethicone. Polydimethyl methoxy oxane, CTFA name is dimethiconol, polydidecyl fluorenyl oxyalkylene having a base group, and CTFA name is amodimethic 〇ne The amine functional group polydimethyloxane. The emulsion droplets generally have a Sauter mean droplet diameter (D3, 2) of from 〇 〇丨 to 2 μm, more preferably from 0.2 to 1 μm in the compositions of the present invention. A suitable method for determining the Sauter mean droplet diameter (1) 3, 2) is carried out according to laser light scattering using an instrument such as a Malvern particle size analyzer. Suitable polyoxylized emulsions for use in the compositions of the present invention are available from polyoxo suppliers such as Dow Corning and GE Silicones. The use of such pre-formed polyoxo-emulsions is preferred for ease of handling and control of the particle size of the polyoxyl oxide. 148372.doc 15 201109035. The pre-formed polyoxoemulsions may generally additionally comprise suitable emulsifiers (such as anionic or nonionic emulsifiers, or mixtures thereof), and may be by chemical emulsification methods such as emulsion polymerization, or by employing high shear mixing. Prepared by mechanical emulsification. Typically, a pre-formed polyoxo-emulsion having a Sauter mean droplet diameter (D3, 2) of less than 0.15 microns is referred to as a microemulsion. Examples of suitable pre-formed polyoxyn emulsions include emulsions DC2-1766, DC2-1784, DC-1785, DC-1786, DC-1788 and microemulsions DC2-1865 and DC2-1870, all available from Dow Corning. DC7051 is the preferred polyoxane. These are all emulsions/microemulsions of dimethyl polyoxyl alcohol. Amine based eucalyptus emulsions (such as DC 2-8177 and DC 939) and SME 253 (available from GE Silicones) are also suitable. Polyoxyn emulsions of a particular class of high molecular weight surface-active block copolymers which have been blended with, for example, the polyoxynoxy emulsion droplets described in WO 03/094874 are also suitable. Among such materials, the polyoxyxide emulsion droplets are preferably formed by a polydiorganotoxime such as the one described above. A preferred form of the surface active block copolymer is according to the following chemical formula: H0(CH2CH20)x(CH(CH3)CH20)y(CH2CH20)xH wherein the average value of X is 4 or greater, and the average value of y is 25 or more. Another preferred form of the surface active block copolymer is according to the formula: (HO(CH2CH20)a(CH(CH3)CH20)b)2-N-CH2-CH2-N((OCH2CH(CH3))b ( OCH2CH2)aOH)2 wherein the average value of a is 2 or more, and the average value of b is 6 or more. Mixtures of any of the above-mentioned polyoxo-oxygen emulsions may also be employed. 148372.doc -16 - 201109035 The above poly-stone emulsion is generally present in the composition of the present invention in an amount ranging from G._i5 wt%, preferably 0.5 to the total weight of the total weight of the composition. 12% by weight. The polyoxime is preferably present in an amount of from 5 to 15% by weight, more preferably (1)%. Additional Ingredients to Improve Efficiency The compositions of the present invention may comprise the following energy and/or consumer acceptability as desired.
該組合物可包含共表面活性劑 物理或清潔性質。 以賦予該組合物美觀、 /、表面活性劑一實例為非離子表面活性劑,其所包含的 t量範圍以該組合物總重量為基礎之重量計為0 5至10重 ϊ ’較佳為〇·7至6重量%。 〇 例如,包含^本發明洗髮精組合物中之代表性非離子表 面活性劑包括脂肪族(crcu) 一級或二級直鏈線性或分支 鏈醇或苯酚與環氧烷(通常為環氧乙烷,且一般具有6至3〇 個環氧乙烷基團)之縮合產物。 其他代表性非離子表面活性劑包括單或二燒基鏈院醇酿 胺。實例包括椰油基單或二乙醇醯胺及椰油基單異丙醇醯 胺。一尤佳之非離子表面活性劑為椰油基單乙醇醯胺。 包含於本發明洗髮精組合物中之額外非離子表面活性劑 為烷基聚葡萄糖苷(APG)。一般,該APG為包括烷基之 APG,其中該烷基連接(視需要通過橋基)至—或多個糖基 嵌段。較佳之APG係以下列化學式界定: R〇-(G)n 148372.doc 201109035 其中R為可飽和或 SI基。 可不飽和之具支鏈或直鏈烷基,及G為 R可表示約C5至約r + , 々C2G之平均烷基鏈長度。較佳地,汉表 不約C8至约C丨2之平均抆 尺表 .Q , ^ 7Λ _基鏈長度。最佳地,R的數值介於 約9 5及、.勺1 〇 · 5間。g可選自「^ D ' 葡箱煃#。6早㈣殘基,且較佳為 〜 "選自包括葡萄糖、木糖、乳糖、果糖、甘 路糖及其衍生物之群。較佳地,G為㈣糖。 聚合作用的程度11係為約1至約1〇或更大的數值。較佳 地’ η的數值介於約1 .至力2 最佳地,η的數值介於約i 3 至約1.5。 · 用於本發明合適之院基聚葡萄糖普可商業購得,且包括 例如以下商品名識別之該等材料:自公司之〇_ix NS10 ’自Henkel公司之Plantaren 12〇〇及心偷削綱〇。 包含於本發明組合物中之其他糖衍生非離子表面活性劑 匕括C]G-C18 N-烷基(Ci-C6)聚羥基脂肪酸醯胺(諸如描述於 例^卿92 〇6154及Us 5 194㈣中之kb N-曱基葡糖 醯fe)、及N-烷氧基聚羥基脂肪酸醯胺(諸如c^_Ci8N_(3_t 氧基丙基)葡糖醯胺)。 共表面活性劑之較佳實例為兩性或雙性離子表面活性 劑’其含量範圍占該組合物總重量之0.5至约1〇重量%,較 佳1至6重量%。 兩性或兩雙離子表面活性劑之實例包括烷基胺氧化物、 烧基甜菜鹼、烷基醯胺基丙基甜菜鹼、烷基磺酸甜菜鹼 (續基甜菜鹼)、烷基甘胺酸鹽、烷基羧酸甘胺酸鹽、烷基 148372.doc -18- 201109035 兩性基乙酸鹽、烷基兩性基丙酸鹽、烷基兩性基甘胺酸 鹽、烧基醯胺基丙基經基確基甜菜驗、醢基牛績酸鹽及醢 基麩胺酸鹽,其中該烷基及醯基具有8至19個碳原子。適 用於本發明洗髮精中之一般的兩性及雙性離子表面活性劑 包括月桂基胺氧化物、椰油基二甲基磺丙基甜菜鹼、月桂 基甜菜鹼、椰油基醯胺基丙基甜菜鹼及椰油基兩性基乙酸 納。The composition may comprise a co-surfactant physical or cleaning property. To give the composition an aesthetic appearance, /, an example of a surfactant is a nonionic surfactant, which comprises a t amount ranging from 0 5 to 10 weights based on the total weight of the composition. 〇·7 to 6 wt%. For example, representative nonionic surfactants comprising the shampoo compositions of the present invention include aliphatic (crcu) primary or secondary linear linear or branched alcohols or phenols and alkylene oxides (usually epoxy B) The condensation product of an alkane, and generally having 6 to 3 oxirane groups. Other representative nonionic surfactants include mono or dialkyl chain alcohol amines. Examples include coco mono or diethanolamine and cocomonoisopropanol oxime. A particularly preferred nonionic surfactant is coco monoethanolamine. The additional nonionic surfactant included in the shampoo compositions of the present invention is an alkyl polyglucoside (APG). Typically, the APG is an APG comprising an alkyl group, wherein the alkyl group is attached (via a bridging group as needed) to - or a plurality of glycosyl blocks. A preferred APG is defined by the following chemical formula: R〇-(G)n 148372.doc 201109035 wherein R is a saturable or SI group. A branched or straight chain alkyl group which may be unsaturated, and G of R may represent an average alkyl chain length of from about C5 to about r + , 々C2G. Preferably, the Han watch does not have an average scale of C8 to about C丨2 . Q , ^ 7Λ _ base chain length. Optimally, the value of R is between about 9.5 and . g may be selected from the group consisting of "^ D ' 葡箱煃#. 6 early (four) residues, and preferably ~ " selected from the group consisting of glucose, xylose, lactose, fructose, gamma sugar and derivatives thereof. Ground, G is (iv) sugar. The degree of polymerization 11 is a value of from about 1 to about 1 Torr or more. Preferably, the value of 'η is between about 1. and force 2. optimally, the value of η is between From about i 3 to about 1.5. - Suitable for hospital-based polydextrose for commercial use in the present invention, and includes such materials as identified by the following trade names: from the company _ix NS10 'Plantaren 12 from Henkel Corporation Other sugar-derived nonionic surfactants included in the compositions of the present invention include C]G-C18 N-alkyl (Ci-C6) polyhydroxy fatty acid decyl amines (such as described in Example qing 92 〇 6154 and Us 5 194 (d) kb N-mercaptoglucoside fe), and N-alkoxy polyhydroxy fatty acid decylamine (such as c ^ _Ci8N_ (3_t oxypropyl) glucosamine A preferred example of a co-surfactant is an amphoteric or zwitterionic surfactant' in an amount ranging from 0.5 to about 1% by weight based on the total weight of the composition. 1 to 6% by weight. Examples of the amphoteric or two-ionic surfactant include alkylamine oxides, burnt betaine, alkylguanidinopropyl betaine, and alkylsulfonic acid betaine (renering betaines). , alkyl glycinate, alkyl carboxylic acid glycinate, alkyl 148372.doc -18- 201109035 amphoteric acetate, alkyl amphopropionate, alkyl amphoglycine, alkyl The amidinopropyl group is based on a ketone test, a sulfhydryl citrate salt and a thiol glutamate, wherein the alkyl group and the fluorenyl group have 8 to 19 carbon atoms. It is suitable for use in the shampoo of the present invention. Typical amphoteric and zwitterionic surfactants include laurylamine oxide, cocodimethyl dimethyl sulfobetaine, lauryl betaine, cocoyl propyl propyl betaine and cocoyl amphoteric Acetic acid.
一尤佳之兩性或雙性離子表面活性劑為椰油基醯胺基丙 基甜菜驗。 任何前述兩性或雙性離子表面活性劑之混合物亦是合適 的。較佳之混合物為椰油基醯胺基丙基甜菜鹼與以上所述 之額外兩丨生或雙性離子表面活性冑彳之混合物。—較佳之其 他兩性或雙性離子表面活性劑為椰油基兩性基乙酸鈉。/、 本發明組合物可包含用於提高效能及/或消費者接受度 之其他成分。該等成分包括芳香劑、染料及色素、pH調節 劑、珠光劑或非透明劑、黏度調節劑、及防腐劑或抗微生 物劑每肩等成分係以可有效實現其目的之含量存在。 一般地,所包含之該箄葙步 寺視而要成分的含量個別地以總組合 物重量計可高達至5重量%。 【實施方式】 本發明進-步藉由以下非限制性實例說 只ιη βυ… 穴丁 71用的 所有百分比係為以總重晋斗 、 里里叶之重量百分比,除非另有陳 述。 148372.doc 19- 201109035 實例1 INCI名稱 灰分% (ad%) 實例1 實例2 實例3 實例4 月桂醇醚硫酸鈉 70 34.28 34.28 34.28 34.28 椰油基醯胺基丙基 甜菜驗 30 10.66 - 10.66 • 揶子醯胺MEA 85 - 2.0 - 2.0 乙二醇二硬脂酸酯 35 4.0 4.0 4.0 4.0 二甲聚矽氧烷醇 DC1788 50 12.0 12.0 12.0 12.0 甘胺酸大豆油 100 4.0 4.0 4.0 4.0 香料 100 0.8 0.8 0.8 0.8 瓜爾經丙基三曱基 氯化銨 100 0.4 0.4 0.4 0.4 氯化納 100 - - 1.0 1.0 丙二醇 100 - - - - 二曱聚矽氧烷醇 DC7123 50 - - - - DMDM乙内醯脲及 3-块-2-丙块基胺基 曱酸丁酯 50 0.2 0.2 0.2 0.2 水 補充適量至 100 補充適量至 100 補充適量至 100 補充適量至 100 INCI名稱 灰分% (ad%) 實例5 實例6 實例7 實例8 月桂醇醚硫酸鈉 70 34.28 34.28 34.28 34.28 椰油基醯胺基丙基 甜菜驗 30 10.66 _ 10.66 椰子醯胺MEA 85 - 2.0 - 2.0 乙二醇二硬脂酸酯 35 4.0 4.0 4.0 4.0 二曱聚矽氧烷醇 DC1788 50 12.0 12.0 8.0 8.0 甘胺酸大豆油 100 4.0 4.0 4.0 4.0 香料 100 0.8 0.8 0.8 0.8 瓜爾羥丙基三甲基 氣化銨 100 0.4 0.4 0.4 0.4 氯化鈉 100 - - 1.0 1.0 丙二醇 100 10.0 10.0 - - 二曱聚矽氧烷醇 DC7123 50 - - 4.0 4.0 DMDM乙内醯脲及 3-破-2-丙快基胺基 曱酸丁酯 50 0.2 0.2 0.2 0.2 水 補充適量至 100 補充適量至 100 補充適量至 100 補充適量至 100 148372.doc -20- 201109035 INCI名稱 灰分% (ad%) 實例9 實例10 實例11 實例12 月桂醇醚硫酸納 70 34.28 34.28 34.28 34.28 椰油基酿胺基丙基 甜菜驗 30 10.66 10.66 - 椰子醢胺MEA 85 - 2.0 - 2.0 乙二醇二硬脂酸酯 35 4.0 4.0 4.0 4.0 二甲聚矽氧烷醇 DC 1788 50 12.0 12.0 12.0 12.0 甘胺酸大豆油 100 3.0 3.0 3.0 3.0 香料 100 0.8 0.8 0.8 0.8 瓜爾經丙基三甲基 氯化銨 100 0.4 0.4 0.4 0.4 揶子油 100 2.0 2.0 2.0 2.0 氯化納 100 - - 1.0 1.0 丙二醇 100 - - - - 二曱聚矽氧烷醇 DC7123 50 - - - - DMDM乙内醯脲及 3-碘-2-丙炔基胺基甲酸 丁酯 50 0.2 0.2 0.2 0.2 水 補充適量至 100 補充適量至 100 補充適量至 100 補充適量至 100 實例2 根據本發明所有發明調配物係根據此製程以當有需要時 之油取代進行製造。在另一個鍋桶中,將至少8%之水加 熱至約80°C。利用高速攪拌,在此鍋桶中加入陽離子(二 十二烷基三甲基氯化銨)表面活性劑、脂肪醇、二級陰離 子表面活性劑(蠟鯨硬脂基硫酸鈉)。當得到均勻分散液 時,將該混合物以相同速度攪拌冷卻降至約45°C。然後將 該混合物添加至於配備有雙勾漿盤及刮刀之高速分散混合 器中之濃縮一級表面活性劑(月桂醇醚硫酸鈉)。該等組分 係以高剪切及在真空條件下進行混合。接著,在相同條件 下,混合剩餘組分。在加水之前添加甘油三酸醋油。剩餘 水係在最後加入該調配物中。 148372.doc -21 - 201109035 實例3 製造以下調配物以評估本發明對合適比較組之效益。彼 者可藉由類似的製程製造。 INCI名稱 灰分% (ad%) 比較1 比較2 比較3 (無凝膠) 比較4 (凝膠) 實例1 (凝膠+油) 實例2 (凝膠+油) 月桂醇醚硫酸鈉 70 20.00 20.00 34.28 34.28 34.28 34.28 挪油基酿胺基 丙基甜菜驗 30 5.33 5.33 10.66 10.66 10.66 _ 椰子醯胺 85 - - - - - 2.0 羧酸乙烯製劑 100 0.4 0.4 - - - - 乙二醇二硬脂 酸酯 35 4.0 4.0 4.0 4.0 4.0 4.0 二曱聚矽氧烷醇 /TEA-DOBS 50 6.0 6.0 12.0 12.0 12.0 12.0 蠟鯨硬脂基硫 酸鈉 100 - - 0.6 0.6 0.6 蠟鯨硬脂醇 100 - - - 1 1 1 氣化二十二烷基 三甲銨 77.5 - 0.06 0.06 0.06 礦物油 100 - 3 - - 1.0 1.0 香料 100 0.8 0.8 0.8 0.8 0.8 0.8 瓜爾羥丙基三 甲基氣化銨 100 0.15 0.15 0.3 0.3 0.3 0.3 瓜爾羥丙基三 甲基氣化銨 100 0.05 0.05 0.1 0.1 0.1 0.1 氯化鈉 100 0.5 0.5 - - - - DMDM乙内醯脲 及3-碘-2-丙炔基 胺基甲酸丁酯 50 0.2 0,2 0.2 0.2 0.2 0.2 水 補充 適量至 100 補充 適量至 100 補充 適量至 100 補充 適量至 100 補充 適量至 100 補充 適量至 100 所評估的效益為濕潤塗覆觸感。 效益 比較1 比較2 比較3 (半劑量) 比較4 (半劑量) 實例1 (半劑量) 濕潤塗覆觸感 3.05 3.2 3.5 3.95(對照比較1有 95%明顯差異) 4.55(對照比較I有 99%明顯差異) 實例4 以下為經由類似之製程製得之洗髮精調配物。 148372.doc -22- 201109035 INCI名稱 灰分% (ad%) 實例1 實例2 實例3 實例4 月桂醇醚硫酸鈉 70 34.28 34.28 34.28 34.28 椰油基醯胺基丙基 甜菜驗 30 10.66 10.66 - 椰子醯胺 85 - 2.0 - 2.0 乙二醇二硬脂酸酯 35 4.0 4.0 4.0 4.0 二甲聚矽氧烷醇 /TEA-DOBS 50 12.0 12.0 12.0 12.0 蠟鯨硬脂基硫酸納 100 0.3 0.3 0.3 0.3 蠟鯨硬脂醇 100 0.5 0.5 0.5 0.5 氯化二十二烧基三 甲銨 77,5 0.03 0.03 - - 氯化十六烷基三甲銨 29 - - 0.085 0.085 三羥甲基丙烷三辛酸 酯/三癸酸酯 100 1.0 1.0 1.0 1.0 香料 100 0.8 0.8 0.8 0.8 瓜爾經丙基三曱基氯 化銨 100 0.4 0.4 0.4 0.4 DMDM乙内醯脲及 3-碘-2-丙炔基胺基 甲酸丁酯 50 0.2 0.2 0.2 0.2 水 補充適量至 100 補充適量至 100 補充適量至 100 補充適量至 100 實例5 爲證明本發明組合物之經改良濕潤塗覆觸感,進行以下 列示調配物間之比較。 INCI名稱 灰分% (ad%) 比較1 (無凝膠, 無油) 比較2 (凝膠) 實例1 實例2 實例3 實例4 月桂醇醚硫酸 鈉 70 34.28 34.28 34.28 34.28 34.28 34.28 挪油基酿胺基 丙基甜菜鹼 30 10.66 10.66 10.66 10.66 - 椰子醯胺MEA 85 - - - 2.0 - 2.0 羧酸乙烯製劑 100 - - - - - - 乙二醇二硬脂 酸酯 35 4.0 4.0 4.0 4.0 4.0 4.0 二甲聚矽氧烷 醇/TEA-DOBS 50 12.0 12.0 12.0 12.0 12.0 12.0 蠟鯨硬脂基硫 酸鈉 100 - 0.3 0.3 0.3 0.3 0.3 148372.doc -23- 201109035 蠟鯨硬脂醇 100 - 0.5 0.5 0.5 0.5 0.5 氯化二十二烷 基三甲銨 77.5 - 0.03 0.03 0.03 * 會 氯化十六烧基 三曱銨 29.0 - 0.085 0.085 氫化至14 稀烴聚合物 100 ** 1.0 1.0 1.0 1.0 香料 100 0.8 0.8 0.8 0.8 0.8 0.8 瓜爾經丙基 三甲基氣化銨 100 0.4 0.4 0.4 0.4 0.4 0.4 DMDM乙内醯 脲及3-碘-2-丙 炔基胺基甲酸 丁酯 50 0.2 0.2 0.2 0.2 0.2 0.2 水 補充 適量至 100 補充 適量至 100 補充 適量至 100 補充 適量至 100 補充 適量至 100 補充 適量至 100 效益 比較1 比較2 實例1 濕潤塗覆觸感 0.5 0.79 (99%差異) 0.81 (99.9% 差異) 148372.doc 24-A particularly preferred amphoteric or zwitterionic surfactant is cocoyl amide-based propyl beet. Mixtures of any of the foregoing amphoteric or zwitterionic surfactants are also suitable. A preferred mixture is a mixture of cocoyl guanidinopropyl betaine and the additional two axillary or zwitterionic surfactants described above. Preferably, the other amphoteric or zwitterionic surfactant is sodium cocoamphoacetate. /, The compositions of the present invention may comprise other ingredients for improved efficacy and/or consumer acceptance. Such ingredients include fragrances, dyes and pigments, pH adjusters, pearlizing agents or non-clear agents, viscosity modifiers, and preservatives or anti-microbial agents, each of which is present in an amount effective to achieve its purpose. Generally, the amount of ingredients included in the step is typically up to 5% by weight based on the total composition weight. [Embodiment] The present invention is further described by the following non-limiting examples. All percentages used for 71 71 71 71 71 71 71 71 71 71 71 71 。 。 。 。 。 。 。 。 。 。 。 。 。 。 。 。 。 。 。 。 。 。 。 。 。 。 148372.doc 19-201109035 Example 1 INCI name ash % (ad%) Example 1 Example 2 Example 3 Example 4 Sodium lauryl ether 70 34.28 34.28 34.28 34.28 Cocoyl guanyl propyl beet test 30 10.66 - 10.66 • 揶Eudecylamine MEA 85 - 2.0 - 2.0 Ethylene glycol distearate 35 4.0 4.0 4.0 4.0 Dimercaptohydroxanol DC1788 50 12.0 12.0 12.0 12.0 Glycine Soybean Oil 100 4.0 4.0 4.0 4.0 Perfume 100 0.8 0.8 0.8 0.8 guar by propyl tridecyl ammonium chloride 100 0.4 0.4 0.4 0.4 sodium chloride 100 - - 1.0 1.0 propylene glycol 100 - - - - dimercapto polyoxyl alkanol DC7123 50 - - - - DMDM carbendazim and 3-block-2-propionyl butyl decanoate 50 0.2 0.2 0.2 0.2 Water supplemented to 100 Supplementary amount to 100 Supplementary amount to 100 Supplementary amount to 100 INCI name ash % (ad%) Example 5 Example 6 Example 7 Example 8 Sodium lauryl ether sulfate 70 34.28 34.28 34.28 34.28 Cocoyl decyl propyl beet test 30 10.66 _ 10.66 Cocoamine MEA 85 - 2.0 - 2.0 Ethylene glycol distearate 35 4.0 4.0 4.0 4.0 II曱Polyoxyalkanol DC1788 50 12.0 12.0 8.0 8.0 Amino acid soybean oil 100 4.0 4.0 4.0 4.0 Perfume 100 0.8 0.8 0.8 0.8 guar hydroxypropyltrimethylammonium oxide 100 0.4 0.4 0.4 0.4 Sodium chloride 100 - - 1.0 1.0 Propylene glycol 100 10.0 10.0 - - Diterpene polyoxyl Alkanol DC7123 50 - - 4.0 4.0 DMDM carbendazim and 3-bromo-2-propionyl butyl decanoate 50 0.2 0.2 0.2 0.2 Water supplemented to 100 Supplementary amount to 100 Supplementary amount to 100 Supplementary amount to 100 148372.doc -20- 201109035 INCI name ash % (ad%) Example 9 Example 10 Example 11 Example 12 Sodium lauryl ether sulfate 70 34.28 34.28 34.28 34.28 Cocoyl-based aminopropyl beet test 30 10.66 10.66 - Coconut meal Amine MEA 85 - 2.0 - 2.0 Ethylene glycol distearate 35 4.0 4.0 4.0 4.0 Dimethyl methoxyalkanol DC 1788 50 12.0 12.0 12.0 12.0 Glycine soy oil 100 3.0 3.0 3.0 3.0 Perfume 100 0.8 0.8 0.8 0.8 Guar by propyltrimethylammonium chloride 100 0.4 0.4 0.4 0.4 Hazelnut oil 100 2.0 2.0 2.0 2.0 Chlorinated sodium 100 - - 1.0 1.0 Propylene glycol 100 - - - - Diterpene polyoxyl alkanol DC7123 50 - - - - DMDM carbendazim and 3-iodo-2-propynylamino Acid butyl ester 0.2 50 0.2 0.2 0.2 Water qs to 100 complementary to the added amount of the added amount of 100 to 100 qs to 100 Example 2 supplemented when necessary to replace the oil produced according to this process for all formulations are prepared according to the present invention. In another pot, at least 8% of the water is heated to about 80 °C. A cationic (dodecylamethylenetrimethylammonium chloride) surfactant, a fatty alcohol, and a secondary anionic surfactant (wax whale stearyl sulfate) were added to the pot using high speed stirring. When a homogeneous dispersion was obtained, the mixture was stirred and cooled to about 45 ° C at the same speed. The mixture was then added to a concentrated primary surfactant (sodium lauryl ether sulfate) in a high speed dispersing mixer equipped with a double pulping tray and a doctor blade. The components are mixed under high shear and under vacuum. Next, the remaining components were mixed under the same conditions. Add triacetin oil before adding water. The remaining water system is added to the formulation at the end. 148372.doc -21 - 201109035 Example 3 The following formulations were made to evaluate the benefits of the present invention for a suitable comparison set. The other can be manufactured by a similar process. INCI Name Ash % (ad%) Comparison 1 Comparison 2 Comparison 3 (no gel) Comparison 4 (gel) Example 1 (gel + oil) Example 2 (gel + oil) Sodium lauryl ether 70 20.00 20.00 34.28 34.28 34.28 34.28 Norse-based aminopropyl beet test 30 5.33 5.33 10.66 10.66 10.66 _ coconut decylamine 85 - - - - - 2.0 Carboxylic acid preparation 100 0.4 0.4 - - - - Ethylene glycol distearate 35 4.0 4.0 4.0 4.0 4.0 4.0 Diterpene polyoxyl alkanol/TEA-DOBS 50 6.0 6.0 12.0 12.0 12.0 12.0 Wax whale stearyl sodium 100 - - 0.6 0.6 0.6 Wax whale stearyl alcohol 100 - - - 1 1 1 gas Tetracamenium trimethylammonium 77.5 - 0.06 0.06 0.06 Mineral oil 100 - 3 - - 1.0 1.0 Perfume 100 0.8 0.8 0.8 0.8 0.8 0.8 Guar hydroxypropyl trimethylated ammonium oxide 100 0.15 0.15 0.3 0.3 0.3 0.3 Guar Hydroxypropyltrimethylammonium hydride 100 0.05 0.05 0.1 0.1 0.1 0.1 Sodium chloride 100 0.5 0.5 - - - - DMDM carbendazim and 3-iodo-2-propynyl butyl carbamate 50 0.2 0, 2 0.2 0.2 0.2 0.2 Water to replenish the appropriate amount to 100 Supplementary amount to 100 Supplementary amount to 100 Supplementary amount to 100 Supplement Appropriate amount to 100 Supplements The right amount to 100 evaluated benefits is a wet coating feel. Benefit comparison 1 Comparison 2 Comparison 3 (half dose) Comparison 4 (half dose) Example 1 (half dose) Wet coating feel 3.05 3.2 3.5 3.95 (control comparison 1 has 95% significant difference) 4.55 (control comparison I has 99% Significant differences) Example 4 The following is a shampoo formulation prepared via a similar process. 148372.doc -22- 201109035 INCI name ash % (ad%) Example 1 Example 2 Example 3 Example 4 Sodium lauryl ether 70 34.28 34.28 34.28 34.28 Cocoyl allylamyl propyl beet test 30 10.66 10.66 - Cocoamide 85 - 2.0 - 2.0 Ethylene glycol distearate 35 4.0 4.0 4.0 4.0 Dimethyl phthalol/TEA-DOBS 50 12.0 12.0 12.0 12.0 Wax whale stearyl sulphate 100 0.3 0.3 0.3 0.3 Wax whale hard fat Alcohol 100 0.5 0.5 0.5 0.5 Tetramethylammonium chloride 77,5 0.03 0.03 - - Cetyltrimethylammonium chloride 29 - - 0.085 0.085 Trimethylolpropane tricaprylate / tridecanoate 100 1.0 1.0 1.0 1.0 Perfume 100 0.8 0.8 0.8 0.8 guar propyl tridecyl ammonium chloride 100 0.4 0.4 0.4 0.4 DMDM carbendazim and 3-iodo-2-propynyl butyl carbamate 50 0.2 0.2 0.2 0.2 Water supplemented to 100 Appropriate amount to 100 Supplementary amount to 100 Supplementary amount to 100 Example 5 To demonstrate the improved wet coating feel of the compositions of the present invention, a comparison between the formulations shown below was performed. INCI name ash % (ad%) Comparison 1 (no gel, no oil) Comparison 2 (gel) Example 1 Example 2 Example 3 Example 4 Sodium lauryl ether 70 34.28 34.28 34.28 34.28 34.28 34.28 Propyl betaine 30 10.66 10.66 10.66 10.66 - Cocoamine MEA 85 - - - 2.0 - 2.0 Carboxylic acid preparation 100 - - - - - - Ethylene glycol distearate 35 4.0 4.0 4.0 4.0 4.0 4.0 Dimerization矽 烷 醇 TE TE TE TE TE TE TE TE TE TE TE TE TE TE TE TE TE TE TE TE TE TE TE TE TE TE TE TE TE TE TE TE TE TE TE TE TE TE TE TE TE TE 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 Dodecyltrimethylammonium 77.5 - 0.03 0.03 0.03 * Will be hexadecyltrifluoroammonium chloride 29.0 - 0.085 0.085 Hydrogenated to 14 dilute hydrocarbon polymer 100 ** 1.0 1.0 1.0 1.0 Perfume 100 0.8 0.8 0.8 0.8 0.8 0.8 Melon Propyltrimethylammonium hydride 100 0.4 0.4 0.4 0.4 0.4 0.4 DMDM carbendazim and butyl 3-iodo-2-propynylcarbamate 50 0.2 0.2 0.2 0.2 0.2 0.2 Water supplemented to 100 replenishment Appropriate amount to 100 Supplementary amount to 100 Supplementary amount to 100 supplements Appropriate amount to 100 Supplement Appropriate amount to 100 Benefits Comparison 1 Comparison 2 Example 1 Wet coating feel 0.5 0.79 (99% difference) 0.81 (99.9% difference) 148372.doc 24-
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US8361450B2 (en) * | 2002-06-04 | 2013-01-29 | The Procter & Gamble Company | Shampoo containing a gel network and a non-guar galactomannan polymer derivative |
US9381382B2 (en) * | 2002-06-04 | 2016-07-05 | The Procter & Gamble Company | Composition comprising a particulate zinc material, a pyrithione or a polyvalent metal salt of a pyrithione and a gel network |
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US8361448B2 (en) * | 2002-06-04 | 2013-01-29 | The Procter & Gamble Company | Shampoo containing a gel network |
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