JP2003113046A - Composition for hair - Google Patents
Composition for hairInfo
- Publication number
- JP2003113046A JP2003113046A JP2001337080A JP2001337080A JP2003113046A JP 2003113046 A JP2003113046 A JP 2003113046A JP 2001337080 A JP2001337080 A JP 2001337080A JP 2001337080 A JP2001337080 A JP 2001337080A JP 2003113046 A JP2003113046 A JP 2003113046A
- Authority
- JP
- Japan
- Prior art keywords
- hair
- component
- acid
- composition
- dihydroxypropyl
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
Landscapes
- Cosmetics (AREA)
Abstract
Description
【0001】[0001]
【産業上の利用分野】本発明は、毛髪用組成物に関し、
さらに詳しくは毛髪のコンディショニング効果に優れ、
低刺激で毛髪および頭皮に対して温和で、かつ生分解性
が良好な毛髪用組成物に関する。FIELD OF THE INVENTION The present invention relates to a hair composition,
More specifically, it has excellent hair conditioning effects,
The present invention relates to a hair composition that is mild to hair and mild to the scalp and has good biodegradability.
【0002】[0002]
【従来の技術】従来、毛髪の汚れを除去する目的で、ア
ニオン界面活性剤を主成分とするシャンプーで洗髪する
が、シャンプーで洗髪すると毛髪の汚れのみならず、毛
髪表面を保護している油分も同時に除去されてしまい、
毛髪の柔軟性が失われ、艶のないくし通りの悪い髪とな
り、毛髪の損傷、枝毛、切れ毛が発生し易くなる。そこ
で毛髪にコンディショニング効果(柔軟性、しっとり
感、サラサラ感、滑り性)を付与する目的で、カチオン
界面活性剤である第4級アンモニウム塩を主成分とする
毛髪用組成物で処理するが、第4級アンモニウム塩を主
成分とする毛髪用組成物を用いた場合、毛髪に対する柔
軟性は優れているものの、しっとり感、サラサラ感、滑
り性に関して十分な効果が得られない場合がある。そこ
で、コンディショニング効果に優れ、乾燥後も良好な感
触を付与するアミドカチオン化合物等を含有する組成物
が提案されている。(特開平4−66520、特開平4
−134022、特開平11−286415)また第4
級アンモニウム塩は毛髪及び頭皮に対する刺激、および
生分解性が時として問題となる場合がある。2. Description of the Related Art Conventionally, for the purpose of removing stains on hair, the hair is washed with a shampoo containing an anionic surfactant as a main component. However, washing the hair with a shampoo not only stains the hair, but also protects the hair surface from oil. Are also removed at the same time,
The softness of the hair is lost, the hair becomes dull and dull, and hair damage, split ends, and broken hair are likely to occur. Therefore, for the purpose of imparting a conditioning effect (softness, moisturizing feel, dry feel, and slipperiness) to the hair, it is treated with a composition for hair containing a quaternary ammonium salt which is a cationic surfactant as a main component. When the composition for hair containing a quaternary ammonium salt as a main component is used, although the softness to hair is excellent, it may not be possible to obtain sufficient effects on moisturizing feeling, dry feeling, and slipperiness. Therefore, a composition containing an amide cation compound or the like, which has an excellent conditioning effect and gives a good feel even after drying, has been proposed. (JP-A-4-66520, JP-A-4-66520
-134022, JP-A-11-286415) and the fourth
Secondary ammonium salts can cause problems with irritation to the hair and scalp, and biodegradability.
【0003】[0003]
【本発明が解決しようとする課題】従って、本発明は、
毛髪用組成物に関し、毛髪のコンディショニング効果に
優れ、低刺激で毛髪および頭皮に対して温和で、かつ生
分解性が良好なコンディショニング剤を使用する毛髪用
組成物を開発することにある。Therefore, the present invention is
Regarding a hair composition, it is an object of the present invention to develop a hair composition which is excellent in hair conditioning effect, is mild, mild to hair and scalp, and has good biodegradability.
【0004】[0004]
【課題を解決するための手段】本発明者らは上記課題を
解決すべく鋭意検討を重ねた結果、(A)下記一般式
(1)
R1CONH(CH2)nN+(R2)2CH2CH(OH)CH2OH・X−
(1)
(式中、R1は直鎖又は分岐した炭素数7〜23の飽和
もしくは不飽和脂肪酸残基、R2は炭素数1〜3のアル
キル基、nは1〜5の整数、Xはハロゲン原子を表
す。)で表されるアミドカチオン型界面活性剤と、
(B)下記一般式(2)
R3CONH(CH2)nN(R4)2 (2)
(式中、R3は直鎖又は分岐した炭素数7〜23の飽和
もしくは不飽和脂肪酸残基、R4は炭素数1〜3のアル
キル基、nは1〜5の整数を表す。)で表されるアミド
アミン化合物と、(C)アミドアミン化合物の中和剤
と、(D)高級アルコールとを配合することにより、上
記要件を満たす毛髪用組成物が得られることを見い出
し、本発明を完成させた。As a result of intensive studies to solve the above problems, the present inventors have (A) the following general formula (1) R 1 CONH (CH 2 ) n N + (R 2 ) 2 CH 2 CH (OH) CH 2 OH · X - (1) ( in the formula, R 1 is a linear or branched, saturated or unsaturated fatty acid residue having a carbon number of 7 to 23, R 2 is 1 to 3 carbon atoms An alkyl group, n is an integer of 1 to 5, and X represents a halogen atom.),
(B) the following general formula (2) R 3 CONH (CH 2) n N (R 4) 2 (2) ( wherein, R 3 is a linear or branched, saturated or unsaturated fatty acid residue having a carbon number of 7-23 Group, R 4 is an alkyl group having 1 to 3 carbon atoms, and n is an integer of 1 to 5), a neutralizing agent for the (C) amidoamine compound, and (D) a higher alcohol. It was found that a hair composition satisfying the above-mentioned requirements can be obtained by blending the above composition, and the present invention has been completed.
【0005】すなわち、本発明によれば毛髪用組成物全
量中に、(A)成分を0.1〜10重量%、(B)成分
を0.1〜5重量%、(C)成分を(B)成分1当量に
対して0.5〜2当量、(D)成分を1〜10重量%と
を配合してなる毛髪用組成物を提供するものである。That is, according to the present invention, in the total amount of the composition for hair, the component (A) is 0.1 to 10% by weight, the component (B) is 0.1 to 5% by weight, and the component (C) is ( A hair composition comprising 0.5 to 2 equivalents of component (B) and 1 to 10% by weight of component (D) is provided.
【0006】[0006]
【発明実施の形態】以下に、本発明の毛髪用組成物につ
いて詳述する。本発明に使用される(A)成分としての
アミドカチオン型界面活性剤としては、高級脂肪酸或い
は高級脂肪酸アルキルエステル、もしくはグリセリドと
ジメチルアミノプロピルアミン等のアミンを公知の脱水
反応、エステル交換反応により得られるアミドアミン化
合物に、水または低級アルコール中あるいは水/低級ア
ルコール混合溶媒中で、エピクロロヒドリンまたは3−
クロロ−1,2−プロパンジオール等を原料として合成
されるものでよく、具体的には、ラウリン酸アミドプロ
ピル−N,N−ジメチル−N−(2,3−ジヒドロキシ
プロピル)アンモニウムクロライド、ミリスチン酸アミ
ドプロピル−N,N−ジメチル−N−(2,3−ジヒド
ロキシプロピル)アンモニウムクロライド、パルミチン
酸アミドプロピル−N,N−ジメチル−N−(2,3−
ジヒドロキシプロピル)アンモニウムクロライド、ステ
アリン酸アミドプロピル−N,N−ジメチル−N−
(2,3−ジヒドロキシプロピル)アンモニウムクロラ
イド、ベヘン酸アミドプロピル−N,N−ジメチル−N
−(2,3−ジヒドロキシプロピル)アンモニウムクロ
ライド、オレイン酸アミドプロピル−N,N−ジメチル
−N−(2,3−ジヒドロキシプロピル)アンモニウム
クロライド、ヤシ脂肪酸アミドプロピル−N,N−ジメ
チル−N−(2,3−ジヒドロキシプロピル)アンモニ
ウムクロライド、パーム脂肪酸アミドプロピル−N,N
−ジメチル−N−(2,3−ジヒドロキシプロピル)ア
ンモニウムクロライド、牛脂脂肪酸アミドプロピル−
N,N−ジメチル−N−(2,3−ジヒドロキシプロピ
ル)アンモニウムクロライド、イソステアリン酸アミド
プロピル−N,N−ジメチル−N−(2,3−ジヒドロ
キシプロピル)アンモニウムクロライド、ラウリン酸ア
ミドエチル−N,N−ジエチル−N−(2,3−ジヒド
ロキシプロピル)アンモニウムクロライド、ミリスチン
酸アミドエチル−N,N−ジエチル−N−(2,3−ジ
ヒドロキシプロピル)アンモニウムクロライド、パルミ
チン酸アミドエチル−N,N−ジエチル−N−(2,3
−ジヒドロキシプロピル)アンモニウムクロライド、ス
テアリン酸アミドエチル−N,N−ジエチル−N−
(2,3−ジヒドロキシプロピル)アンモニウムクロラ
イド、ベヘン酸アミドエチル−N,N−ジエチル−N−
(2,3−ジヒドロキシプロピル)アンモニウムクロラ
イド、オレイン酸アミドエチル−N,N−ジエチル−N
−(2,3−ジヒドロキシプロピル)アンモニウムクロ
ライド、ヤシ脂肪酸アミドエチル−N,N−ジエチル−
N−(2,3−ジヒドロキシプロピル)アンモニウムク
ロライド、パーム脂肪酸アミドエチル−N,N−ジエチ
ル−N−(2,3−ジヒドロキシプロピル)アンモニウ
ムクロライド、牛脂脂肪酸アミドエチル−N,N−ジエ
チル−N−(2,3−ジヒドロキシプロピル)アンモニ
ウムクロライド、イソステアリン酸アミドエチル−N,
N−ジエチル−N−(2,3−ジヒドロキシプロピル)
アンモニウムクロライド、ラウリン酸アミドプロピル−
N,N−ジエチル−N−(2,3−ジヒドロキシプロピ
ル)アンモニウムクロライド、ミリスチン酸アミドプロ
ピル−N,N−ジエチル−N−(2,3−ジヒドロキシ
プロピル)アンモニウムクロライド、パルミチン酸アミ
ドプロピル−N,N−ジエチル−N−(2,3−ジヒド
ロキシプロピル)アンモニウムクロライド、ステアリン
酸アミドプロピル−N,N−ジエチル−N−(2,3−
ジヒドロキシプロピル)アンモニウムクロライド、ベヘ
ン酸アミドプロピル−N,N−ジエチル−N−(2,3
−ジヒドロキシプロピル)アンモニウムクロライド、オ
レイン酸アミドプロピル−N,N−ジエチル−N−
(2,3−ジヒドロキシプロピル)アンモニウムクロラ
イド、ヤシ脂肪酸アミドプロピル−N,N−ジエチル−
N−(2,3−ジヒドロキシプロピル)アンモニウムク
ロライド、パーム脂肪酸アミドプロピル−N,N−ジエ
チル−N−(2,3−ジヒドロキシプロピル)アンモニ
ウムクロライド、牛脂脂肪酸アミドプロピル−N,N−
ジエチル−N−(2,3−ジヒドロキシプロピル)アン
モニウムクロライド、イソステアリン酸アミドプロピル
−N,N−ジエチル−N−(2,3−ジヒドロキシプロ
ピル)アンモニウムクロライド等が挙げられる。これら
の中でもステアリン酸アミドプロピル−N,N−ジメチ
ル−N−(2,3−ジヒドロキシプロピル)アンモニウ
ムクロライド、ベヘン酸アミドプロピル−N,N−ジメ
チル−N−(2,3−ジヒドロキシプロピル)アンモニ
ウムクロライドが特に好適に用いられる。本発明では、
これらのアミドカチオン型界面活性剤の中から1種又は
2種以上を任意に用いることができる。BEST MODE FOR CARRYING OUT THE INVENTION The hair composition of the present invention is described in detail below. As the amide cation type surfactant as the component (A) used in the present invention, higher fatty acid or higher fatty acid alkyl ester, or glyceride and amine such as dimethylaminopropylamine are obtained by known dehydration reaction or transesterification reaction. The resulting amidoamine compound is added to epichlorohydrin or 3-, in water or a lower alcohol or a water / lower alcohol mixed solvent.
It may be synthesized using chloro-1,2-propanediol or the like as a raw material, and specifically, lauric acid amidopropyl-N, N-dimethyl-N- (2,3-dihydroxypropyl) ammonium chloride, myristic acid Amidopropyl-N, N-dimethyl-N- (2,3-dihydroxypropyl) ammonium chloride, amidopropyl palmitate-N, N-dimethyl-N- (2,3-
Dihydroxypropyl) ammonium chloride, stearamide propyl-N, N-dimethyl-N-
(2,3-Dihydroxypropyl) ammonium chloride, behenic acid amide propyl-N, N-dimethyl-N
-(2,3-Dihydroxypropyl) ammonium chloride, oleic acid amidopropyl-N, N-dimethyl-N- (2,3-dihydroxypropyl) ammonium chloride, coconut fatty acid amidopropyl-N, N-dimethyl-N- ( 2,3-dihydroxypropyl) ammonium chloride, palm fatty acid amidopropyl-N, N
-Dimethyl-N- (2,3-dihydroxypropyl) ammonium chloride, tallow fatty acid amide propyl-
N, N-dimethyl-N- (2,3-dihydroxypropyl) ammonium chloride, isostearic acid amidopropyl-N, N-dimethyl-N- (2,3-dihydroxypropyl) ammonium chloride, lauric acid amidoethyl-N, N -Diethyl-N- (2,3-dihydroxypropyl) ammonium chloride, myristic acid amidoethyl-N, N-diethyl-N- (2,3-dihydroxypropyl) ammonium chloride, palmitic acid amidoethyl-N, N-diethyl-N -(2,3
-Dihydroxypropyl) ammonium chloride, stearic acid amidoethyl-N, N-diethyl-N-
(2,3-Dihydroxypropyl) ammonium chloride, behenic acid amidoethyl-N, N-diethyl-N-
(2,3-Dihydroxypropyl) ammonium chloride, oleic acid amidoethyl-N, N-diethyl-N
-(2,3-Dihydroxypropyl) ammonium chloride, coconut fatty acid amide ethyl-N, N-diethyl-
N- (2,3-dihydroxypropyl) ammonium chloride, palm fatty acid amide ethyl-N, N-diethyl-N- (2,3-dihydroxypropyl) ammonium chloride, tallow fatty acid amide ethyl-N, N-diethyl-N- (2 , 3-Dihydroxypropyl) ammonium chloride, isostearamide amidoethyl-N,
N-diethyl-N- (2,3-dihydroxypropyl)
Ammonium chloride, lauric acid amidopropyl-
N, N-diethyl-N- (2,3-dihydroxypropyl) ammonium chloride, myristic acid amidopropyl-N, N-diethyl-N- (2,3-dihydroxypropyl) ammonium chloride, palmitic acid amidopropyl-N, N-diethyl-N- (2,3-dihydroxypropyl) ammonium chloride, stearic acid amidopropyl-N, N-diethyl-N- (2,3-
Dihydroxypropyl) ammonium chloride, behenamideamidopropyl-N, N-diethyl-N- (2,3
-Dihydroxypropyl) ammonium chloride, oleic acid amidopropyl-N, N-diethyl-N-
(2,3-Dihydroxypropyl) ammonium chloride, coconut fatty acid amidopropyl-N, N-diethyl-
N- (2,3-dihydroxypropyl) ammonium chloride, palm fatty acid amide propyl-N, N-diethyl-N- (2,3-dihydroxypropyl) ammonium chloride, tallow fatty acid amide propyl-N, N-
Examples thereof include diethyl-N- (2,3-dihydroxypropyl) ammonium chloride and isostearamide propyl-N, N-diethyl-N- (2,3-dihydroxypropyl) ammonium chloride. Among these, stearic acid amidopropyl-N, N-dimethyl-N- (2,3-dihydroxypropyl) ammonium chloride and behenic acid amidopropyl-N, N-dimethyl-N- (2,3-dihydroxypropyl) ammonium chloride Are particularly preferably used. In the present invention,
Among these amide cation type surfactants, one kind or two or more kinds can be optionally used.
【0007】(A)成分の毛髪用組成物中の配合量は、
0.1〜10重量%、好ましくは0.5〜8重量%、よ
り好ましくは1〜5重量%が好ましい。0.1重量%未
満では毛髪に十分なコンディショニング効果が得られ
ず、10重量%を越えても効果が向上せず好ましくな
い。The amount of component (A) in the hair composition is
0.1 to 10% by weight, preferably 0.5 to 8% by weight, more preferably 1 to 5% by weight is preferable. If it is less than 0.1% by weight, a sufficient conditioning effect for hair cannot be obtained, and if it exceeds 10% by weight, the effect is not improved, which is not preferable.
【0008】本発明に使用される(B)成分としてのア
ミドアミン化合物としては、上記アミドカチオン型界面
活性剤の中間体として得られる、アミドアミン化合物と
同様のものでよく、具体的には、ラウリン酸ジメチルア
ミノプロピルアミド、ミリスチン酸ジメチルアミノプロ
ピルアミド、パルミチン酸ジメチルアミノプロピルアミ
ド、ステアリン酸ジメチルアミノプロピルアミド、ベヘ
ン酸ジメチルアミノプロピルアミド、オレイン酸ジメチ
ルアミノプロピルアミド、ヤシ脂肪酸ジメチルアミノプ
ロピルアミド、パーム脂肪酸ジメチルアミノプロピルア
ミド、牛脂脂肪酸ジメチルアミノプロピルアミド、イソ
ステアリン酸ジメチルアミノプロピルアミド、ラウリン
酸ジエチルアミノエチルアミド、ミリスチン酸ジエチル
アミノエチルアミド、パルミチン酸ジエチルアミノエチ
ルアミド、ステアリン酸ジエチルアミノエチルアミド、
ベヘン酸ジエチルアミノエチルアミド、オレイン酸ジエ
チルアミノエチルアミド、ヤシ脂肪酸ジエチルアミノエ
チルアミド、パーム脂肪酸ジエチルアミノエチルアミ
ド、牛脂脂肪酸ジエチルアミノエチルアミド、イソステ
アリン酸ジエチルアミノエチルアミド、ラウリン酸ジエ
チルアミノプロピルアミド、ミリスチン酸ジエチルアミ
ノプロピルアミド、パルミチン酸ジエチルアミノプロピ
ルアミド、ステアリン酸ジエチルアミノプロピルアミ
ド、ベヘン酸ジエチルアミノプロピルアミド、オレイン
酸ジエチルアミノプロピルアミド、ヤシ脂肪酸ジエチル
アミノプロピルアミド、パーム脂肪酸ジエチルアミノプ
ロピルアミド、牛脂脂肪酸ジエチルアミノプロピルアミ
ド、イソステアリン酸ジエチルアミノプロピルアミド等
のアミドアミン化合物が挙げられる。これらの中でもス
テアリン酸ジメチルアミノプロピルアミド、ステアリン
酸ジエチルアミノエチルアミドが特に好適に用いられ
る。本発明では、これらのアミドアミン化合物の中から
1種又は2種以上を任意に用いることができる。The amidoamine compound as the component (B) used in the present invention may be the same as the amidoamine compound obtained as an intermediate of the above amide cation type surfactant, and specifically, lauric acid. Dimethylaminopropylamide, myristic acid dimethylaminopropylamide, palmitic acid dimethylaminopropylamide, stearic acid dimethylaminopropylamide, behenic acid dimethylaminopropylamide, oleic acid dimethylaminopropylamide, coconut fatty acid dimethylaminopropylamide, palm fatty acid dimethyl Aminopropylamide, tallow fatty acid dimethylaminopropylamide, isostearic acid dimethylaminopropylamide, lauric acid diethylaminoethylamide, myristic acid diethylaminoethylamid , Palmitic acid diethylaminoethylamide, diethylaminoethyl stearamide,
Behenic acid diethylaminoethylamide, oleic acid diethylaminoethylamide, coconut fatty acid diethylaminoethylamide, palm fatty acid diethylaminoethylamide, tallow fatty acid diethylaminoethylamide, isostearic acid diethylaminoethylamide, lauric acid diethylaminopropylamide, myristic acid diethylaminopropylamide, palmitic acid Amidoamine compounds such as diethylaminopropylamide, stearic acid diethylaminopropylamide, behenic acid diethylaminopropylamide, oleic acid diethylaminopropylamide, coconut fatty acid diethylaminopropylamide, palm fatty acid diethylaminopropylamide, tallow fatty acid diethylaminopropylamide, isostearic acid diethylaminopropylamide And the like. Among these, stearic acid dimethylaminopropylamide and stearic acid diethylaminoethylamide are particularly preferably used. In the present invention, one kind or two or more kinds can be arbitrarily used from these amidoamine compounds.
【0009】(B)成分の毛髪用組成物中の配合量は、
0.1〜5重量%、特に1〜3重量%が好ましい。0.
1重量%未満では毛髪に十分なコンディショニング効果
が得られず、5重量%を越えても効果が向上せず好まし
くない。The blending amount of the component (B) in the hair composition is
0.1 to 5% by weight, particularly 1 to 3% by weight is preferable. 0.
If it is less than 1% by weight, a sufficient conditioning effect for hair cannot be obtained, and if it exceeds 5% by weight, the effect is not improved, which is not preferable.
【0010】(C)成分のアミドアミン化合物の中和剤
としては、有機酸、無機酸、酸性アミノ酸等が挙げら
れ、具体的には、乳酸、グリコール酸、クエン酸、コハ
ク酸、リンゴ酸、塩酸、硫酸、リン酸、グルタミン酸、
アスパラギン酸等が挙げられ、これらの中でも乳酸、ク
エン酸が特に好適に用いられる。本発明では、これらの
中和剤の中から1種又は2種以上を任意に用いることが
できる。Examples of the neutralizing agent for the amidoamine compound as the component (C) include organic acids, inorganic acids, acidic amino acids, and the like. Specifically, lactic acid, glycolic acid, citric acid, succinic acid, malic acid, hydrochloric acid. , Sulfuric acid, phosphoric acid, glutamic acid,
Examples thereof include aspartic acid, and among these, lactic acid and citric acid are particularly preferably used. In the present invention, one or two or more of these neutralizing agents can be optionally used.
【0011】(C)成分の毛髪用組成物中の配合量は、
(B)成分のアミドアミン化合物1当量に対して0.5
〜2当量、特に0.6〜1.4当量が好ましい。本発明
の毛髪用組成物のpH値は3〜6が好ましく、0.5当
量未満、もしくは2当量を越える場合には上記pHが得
られない場合がある。The blending amount of the component (C) in the hair composition is
0.5 for 1 equivalent of the amidoamine compound of the component (B)
~ 2 equivalents, particularly 0.6-1.4 equivalents are preferred. The pH value of the hair composition of the present invention is preferably 3 to 6, and if the pH value is less than 0.5 equivalent or exceeds 2 equivalents, the above pH may not be obtained.
【0012】(D)成分の高級アルコールとしては、具
体的には、ミリスチルアルコール、セチルアルコール、
ステアリルアルコール、セトステアリルアルコール、ベ
ヘニルアルコール、バチルアルコール、イソステアリル
アルコール等が挙げられ、これらの中でもセトステアリ
ルアルコール、ベヘニルアルコールが特に好適に用いら
れる。本発明では、これらの高級アルコールの中から1
種又は2種以上を任意に用いることができる。Specific examples of the higher alcohol as the component (D) include myristyl alcohol, cetyl alcohol,
Examples thereof include stearyl alcohol, cetostearyl alcohol, behenyl alcohol, batyl alcohol, isostearyl alcohol, and of these, cetostearyl alcohol and behenyl alcohol are particularly preferably used. In the present invention, one of these higher alcohols is used.
One kind or two or more kinds can be optionally used.
【0013】(D)成分の毛髪用組成物中の配合量は、
1〜10重量%、特に3〜8重量%が好ましい。1重量
%未満では、期待される効果が不十分となり、また10
重量%を越えて配合しても使用後の感触が悪くなり好ま
しくない。The blending amount of the component (D) in the hair composition is
1 to 10% by weight, particularly 3 to 8% by weight is preferable. If the amount is less than 1% by weight, the expected effect becomes insufficient, and 10
Even if it is blended in excess of weight%, the feel after use becomes unfavorable.
【0014】本発明は、以上の各成分を特定の配合組成
で混合することによって製造される。その配合組成は、
開発担当者が通常行っている配合試験によって決定する
ことができる。The present invention is produced by mixing the above components in a specific composition. Its composition is
It can be determined by the compounding test which the person in charge of development usually performs.
【0015】本発明の毛髪用組成物には、さらに化粧
料、医薬品などに通常使用される界面活性剤、薬効剤、
抗炎症剤、殺菌剤、防腐剤、紫外線吸収剤、酸化防止
剤、有機および無機粉体、粘度調整剤、色素などを必要
に応じて配合することができる。また、発明の効果を損
なわない範囲で固形油分、半固形油分を加えることがで
きる。具体的には、化粧料などで通常使用されるもので
よく、使用目的や要求機能などにより適宜選択され、例
えば、流動パラフィン、ワセリン、スクワラン等の炭化
水素類、イソプロピルパルミテート、オクタン酸セチ
ル、オレイン酸オレイル等のエステル油、ポリオキシエ
チレンステアリルエーテル、トリオクタン酸グリセリ
ル、ポリグリセリン脂肪酸エステル、ポリオキシエチレ
ン脂肪酸エステル、ポリオキシエチレンソルビタン脂肪
酸エステル等の非イオン界面活性剤、ツバキ油、オリー
ブ油、アボガド油、ホホバ油等の動植物油脂類、メチル
ポリシロキサン、メチルフェニルポリシロキサン、環状
シリコーン等のシリコーン類、カチオン化セルロース、
カチオン化グアガム、ジアリルジメチルアンモニウム系
高分子等の陽イオン変性水溶性高分子類、カチオン化セ
ルロース、カチオン化グアガム、ジアリルジメチルアン
モニウム系高分子等の陽イオン変性水溶性高分子類、エ
チレングリコール、ジエチレングリコール、グリセリン
等の保湿剤、香料などが挙げられる。The hair composition of the present invention further comprises a surfactant, a medicinal agent, which are commonly used in cosmetics, pharmaceuticals, etc.
Anti-inflammatory agents, bactericides, preservatives, ultraviolet absorbers, antioxidants, organic and inorganic powders, viscosity modifiers, pigments and the like can be added as necessary. Further, solid oil and semi-solid oil can be added within a range that does not impair the effects of the invention. Specifically, it may be one usually used in cosmetics and the like, and is appropriately selected depending on the purpose of use and required function, for example, liquid paraffin, vaseline, hydrocarbons such as squalane, isopropyl palmitate, cetyl octanoate, Nonionic surfactants such as oleyl oleate and other ester oils, polyoxyethylene stearyl ether, glyceryl trioctanoate, polyglycerin fatty acid esters, polyoxyethylene fatty acid esters, polyoxyethylene sorbitan fatty acid esters, camellia oil, olive oil, avocado oil , Animal and vegetable oils and fats such as jojoba oil, methylpolysiloxane, methylphenylpolysiloxane, silicones such as cyclic silicone, cationized cellulose,
Cationized guar gum, cation-modified water-soluble polymers such as diallyldimethylammonium polymers, cationized cellulose, cationized guar gum, cation-modified water-soluble polymers such as diallyldimethylammonium polymers, ethylene glycol, diethylene glycol , Moisturizing agents such as glycerin, and fragrances.
【0016】[0016]
【実施例】次に、本発明を実施例により更に詳細に説明
するが、本発明は実施例に限定されるものではない。な
お、タンパク質変性率試験によるアミドカチオン型界面
活性剤、アミドアミン化合物の中和塩と4級アンモニウ
ム塩の比較を表1に示した。また、実施例1〜15及び
比較例1〜10を常法により調製し、効果の測定を実施
し、結果を表2〜表6に示した。含有量は重量%であ
る。EXAMPLES Next, the present invention will be described in more detail by way of examples, but the present invention is not limited to the examples. Table 1 shows a comparison between the amide cation type surfactant, the neutralized salt of the amidoamine compound and the quaternary ammonium salt in the protein denaturation rate test. In addition, Examples 1 to 15 and Comparative Examples 1 to 10 were prepared by a conventional method, the effects were measured, and the results are shown in Tables 2 to 6. The content is% by weight.
【0017】本実施例中で用いた試験方法は下記の通り
である。
(タンパク質変性率試験法)水系高速液体クロマトグラ
フィーを用いて卵白アルブミンpH7緩衝溶液に試料濃
度1%になるように試料を加え、添加24時間後の卵白
アルブミン変性率を220nmの吸収ピークを用いて測
定した。アミドアミン化合物の中和は当量中和とした。
変性率(%)=(Ho−Hs)/Ho×100
Ho:卵白アルブミンの220nm吸収ピークの高さ
Hs:卵白アルブミン緩衝溶液に試料を加えた時の22
0nm吸収ピークの高さ
評価の基準を次のように設定した。
◎・・・卵白アルブミン変性率 30%未満
○・・・卵白アルブミン変性率 30%以上60%未満
△・・・卵白アルブミン変性率 60%以上80%未満
×・・・卵白アルブミン変性率 80%以上The test methods used in this example are as follows. (Protein denaturation rate test method) A sample was added to an ovalbumin pH7 buffer solution at a sample concentration of 1% using aqueous high performance liquid chromatography, and the ovalbumin denaturation rate 24 hours after addition was measured using an absorption peak at 220 nm. It was measured. Neutralization of the amidoamine compound was equivalent to neutralization. Denaturation rate (%) = (Ho-Hs) / Ho × 100 Ho: height of 220 nm absorption peak of ovalbumin Hs: 22 when sample is added to ovalbumin buffer solution
The standard for evaluating the height of the 0 nm absorption peak was set as follows. ◎ ・ ・ ・ Ovalbumin denaturation rate less than 30% ○ ・ ・ ・ Ovalbumin denaturation rate 30% or more but less than 60% △ ・ ・ ・ Ovalbumin denaturation rate 60% or more and less than 80% × ・ ・ ・ Ovalbumin denaturation rate 80% or more
【0018】(柔軟性、しっとり感、サラサラ感、滑り
性)と(総合評価)
調整した組成物を女性20名の専門パネラーにて、髪の
柔軟性、髪のしっとり感、髪のサラサラ感、髪の滑り性
を官能的に比較し、下記基準で評価した。
◎:良いと答えた人が18人以上の場合
○:良いと答えた人が14〜17人の場合
△:良いと答えた人が8〜13人の場合
×:良いと答えた人が7人以下の場合
また総合評価については、官能評価の結果をポイント制
(◎:3ポイント、○:2ポイント、△:1ポイント、
×:0ポイント)にしてその合計より、下記基準で評価
した。
◎:12ポイント以上
○:8〜11ポイント
△:4〜7ポイント
×:3ポイント以下(Flexibility, moisturizing feeling, dry feeling, slipperiness) and (comprehensive evaluation) The prepared composition was prepared by 20 female professional panelists for flexibility of hair, moisturizing feeling of hair, smooth feeling of hair, The slipperiness of the hair was sensory compared and evaluated according to the following criteria. ◎: When the number of people who answered good was 18 or more ○: When the number of people who answered good was 14 to 17 △: When the number of people who answered good was 8 to 13 ×: The number of people who answered good In the case of less than or equal to the number of people or for comprehensive evaluation, the results of the sensory evaluation are point system (◎: 3 points, ○: 2 points, △: 1 point
X: 0 points), and the total was evaluated according to the following criteria. ◎: 12 points or more ○: 8 to 11 points △: 4 to 7 points ×: 3 points or less
【0019】[0019]
【表1】 [Table 1]
【0020】[0020]
【表2】 [Table 2]
【0021】[0021]
【表3】 [Table 3]
【0022】[0022]
【表4】 [Table 4]
【0023】[0023]
【表5】 [Table 5]
【0024】[0024]
【表6】 [Table 6]
【0025】実施例1〜15及び比較例1〜10より明
らかなように、本発明の毛髪用組成物は、髪の柔軟性、
髪のしっとり感、髪のサラサラ感、髪の滑り性及び総合
評価で、いずれも優れた性能を示した。As is clear from Examples 1 to 15 and Comparative Examples 1 to 10, the hair composition of the present invention has
The moist feeling of hair, the feeling of smoothness of hair, the slipperiness of hair, and the comprehensive evaluation all showed excellent performance.
【0026】[0026]
【発明の効果】上記記載のごとく、本発明は毛髪に第4
級アンモニウム塩同等の柔軟性と、第4級アンモニウム
塩では不十分であった、滑り性、サラサラ感を付与する
ことに優れ、また低刺激で生分解性の良好な毛髪用組成
物を提供することは明らかである。As described above, the present invention can be applied to the hair
A composition for hair, which has flexibility equivalent to that of a quaternary ammonium salt, is excellent in imparting a slipperiness and a feeling of smoothness which are insufficient with a quaternary ammonium salt, and has low irritation and good biodegradability is provided. That is clear.
Claims (2)
もしくは不飽和脂肪酸残基、R2は炭素数1〜3のアル
キル基、nは1〜5の整数、Xはハロゲン原子を表
す。)で表されるアミドカチオン型界面活性剤と、
(B)下記一般式(2) R3CONH(CH2)nN(R4)2 (2) (式中、R3は直鎖又は分岐した炭素数7〜23の飽和
もしくは不飽和脂肪酸残基、R4は炭素数1〜3のアル
キル基、nは1〜5の整数を表す。)で表されるアミド
アミン化合物と、(C)アミドアミン化合物の中和剤
と、(D)高級アルコールを含有する毛髪用組成物。1. (A) The following general formula (1) R 1 CONH (CH 2 ) n N + (R 2 ) 2 CH 2 CH (OH) CH 2 OH.X − (1) (wherein R 1 Is a linear or branched saturated or unsaturated fatty acid residue having 7 to 23 carbon atoms, R 2 is an alkyl group having 1 to 3 carbon atoms, n is an integer of 1 to 5, and X is a halogen atom. An amide cation type surfactant,
(B) the following general formula (2) R 3 CONH (CH 2) n N (R 4) 2 (2) ( wherein, R 3 is a linear or branched, saturated or unsaturated fatty acid residue having a carbon number of 7-23 Group, R 4 is an alkyl group having 1 to 3 carbon atoms, and n is an integer of 1 to 5), a neutralizing agent for the (C) amidoamine compound, and (D) a higher alcohol. A composition for hair containing.
1〜10重量%、(B)成分を0.1〜5重量%、
(C)成分を(B)成分1当量に対して0.5〜2当
量、(D)成分を1〜10重量%とを配合してなる請求
項1の毛髪用組成物。2. The component (A) is added to the total amount of the composition for hair in an amount of 0.
1 to 10% by weight, the component (B) is 0.1 to 5% by weight,
The hair composition according to claim 1, wherein the component (C) is blended in an amount of 0.5 to 2 equivalents with respect to 1 equivalent of the component (B), and the component (D) is included in an amount of 1 to 10% by weight.
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Cited By (2)
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WO2006109877A1 (en) * | 2005-04-11 | 2006-10-19 | Kao Corporation | Hair cosmetic |
WO2019049722A1 (en) * | 2017-09-07 | 2019-03-14 | 株式会社Adeka | Hair cosmetic composition containing aqueous gelling agent, and method for producing aqueous gelling agent and hair cosmetic composition |
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JPH0466520A (en) * | 1990-07-02 | 1992-03-02 | Kanebo Ltd | Hair rinsing agent composition |
US5288484A (en) * | 1992-05-15 | 1994-02-22 | Anne Tashjian | Cationic cellulose derivative containing fatty quaternum groups in a pre-shampoo conditioning composition |
JPH10273426A (en) * | 1997-01-30 | 1998-10-13 | Sanyo Chem Ind Ltd | Agent for treating hair |
JPH11286415A (en) * | 1998-02-10 | 1999-10-19 | Johnson & Johnson Consumer Co Inc | Hair conditioning composition |
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Cited By (6)
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WO2006109877A1 (en) * | 2005-04-11 | 2006-10-19 | Kao Corporation | Hair cosmetic |
JP2006290796A (en) * | 2005-04-11 | 2006-10-26 | Kao Corp | Hair cosmetic |
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WO2019049722A1 (en) * | 2017-09-07 | 2019-03-14 | 株式会社Adeka | Hair cosmetic composition containing aqueous gelling agent, and method for producing aqueous gelling agent and hair cosmetic composition |
JPWO2019049722A1 (en) * | 2017-09-07 | 2020-08-20 | 株式会社Adeka | Hair cosmetic composition containing water-based gelling agent, and method for producing the water-based gelling agent and hair cosmetic composition |
JP7179004B2 (en) | 2017-09-07 | 2022-11-28 | 株式会社Adeka | HAIR COSMETIC COMPOSITION CONTAINING AQUEOUS GELLING AGENT, AND METHOD FOR MANUFACTURING SAME AQUEOUS GELLING AGENT AND HAIR COSMETIC COMPOSITION |
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