JP3495446B2 - Hair cosmetics - Google Patents

Hair cosmetics

Info

Publication number
JP3495446B2
JP3495446B2 JP03668295A JP3668295A JP3495446B2 JP 3495446 B2 JP3495446 B2 JP 3495446B2 JP 03668295 A JP03668295 A JP 03668295A JP 3668295 A JP3668295 A JP 3668295A JP 3495446 B2 JP3495446 B2 JP 3495446B2
Authority
JP
Japan
Prior art keywords
hair
modified silicone
cosmetic composition
silicone
extract
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Fee Related
Application number
JP03668295A
Other languages
Japanese (ja)
Other versions
JPH08231348A (en
Inventor
裕子 鈴木
潤 亀谷
康治 森田
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Kao Corp
Original Assignee
Kao Corp
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Filing date
Publication date
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Priority to JP03668295A priority Critical patent/JP3495446B2/en
Publication of JPH08231348A publication Critical patent/JPH08231348A/en
Application granted granted Critical
Publication of JP3495446B2 publication Critical patent/JP3495446B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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  • Compositions Of Macromolecular Compounds (AREA)

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】本発明は、毛髪のパサツキや髪色
の変化等のダメージを防止することができ、感触が良好
で、安定性及び安全性に優れた毛髪化粧料に関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a hair cosmetic composition which can prevent damage to the hair such as dryness and change in hair color, has a good feel, and is excellent in stability and safety.

【0002】[0002]

【従来の技術及び発明が解決しようとする課題】毛髪は
常に環境に晒され、紫外線、空気の乾燥、熱等によりパ
サついたり、赤茶色に変色するなど、ダメージを受けや
すい。このとき、毛髪は活性酸素により表面酸化を受け
ていると考えられ、様々な環境因子の中でも紫外線は活
性酸素の発生要因として重要であることがわかってい
る。
2. Description of the Related Art Hair is always exposed to the environment, and is easily damaged by ultraviolet rays, drying of air, heat, etc., such as dryness and discoloration of reddish brown. At this time, it is considered that the hair is surface-oxidized by active oxygen, and it is known that ultraviolet rays are important as a factor for generating active oxygen among various environmental factors.

【0003】従来、このような毛髪のダメージを防止す
る目的で、高重合ジメチルポリシロキサンと、紫外線防
止剤としてベンゾフェノン類を含有した毛髪化粧料(特
開平4−224508号)、高分子シリコーンと酸化防
止剤を含有した毛髪化粧料(特開平1−211515
号)等が提案されている。しかしながら、これらの毛髪
化粧料は、ダメージ防止効果等の点で充分満足できるも
のではなく、しかも光安定性や安全性の点でも問題があ
った。
Conventionally, for the purpose of preventing such damage to hair, hair cosmetics containing highly polymerized dimethylpolysiloxane and benzophenones as UV inhibitors (JP-A-4-224508), polymeric silicone and oxidation. Hair cosmetics containing an inhibitor (Japanese Patent Application Laid-Open No. 1-211515)
No.) etc. have been proposed. However, these hair cosmetics are not sufficiently satisfactory in terms of damage prevention effect and the like, and also have problems in light stability and safety.

【0004】従って、本発明の目的は、紫外線等による
毛髪のダメージを防止することができ、安定性及び安全
性に優れた毛髪化粧料を提供することにある。
Therefore, an object of the present invention is to provide a hair cosmetic composition which can prevent damage to the hair due to ultraviolet rays and the like and is excellent in stability and safety.

【0005】[0005]

【課題を解決するための手段】かかる実情において、本
発明者らは鋭意研究を行った結果、不揮発性シリコーン
類と特定の植物、その抽出物又は圧搾物を組合わせて用
いれば、活性酸素による毛髪の損傷、色調の変化等のダ
メージを抑えることができ、しかも感触が良好で、安定
性及び安全性に優れた毛髪化粧料が得られることを見出
し、本発明を完成した。
Under such circumstances, as a result of intensive studies, the present inventors have found that when non-volatile silicones are used in combination with a specific plant, its extract or squeezed product, The present invention has been completed by finding that a hair cosmetic composition that can suppress damage to hair, change in color tone, and the like, and that has a good feel, and that is excellent in stability and safety can be obtained.

【0006】すなわち、本発明は、次の成分(A)及び
(B): (A)不揮発性シリコーン類、 (B)ゴマ、ブルーベリー及びハマメリスから選ばれる
植物、その抽出物又は圧搾物を含有し、水溶性キチン誘
導体、ビニルピロリドンとジアルキルアミノアルキルメ
タクリレートの共重合体、ピロリドンカルボン酸、乳
酸、プロリン及び酸性アミノ酸を含まない、シャンプ
ー、リンス及びヘアコンディショナーから選ばれる毛髪
化粧料を提供するものである。
Namely, the present invention comprises the following components (A) and (B): (A) non-volatile silicones, contain (B) sesame, plants selected from blueberry and hamamelis, its extract or squeezed product , Water-soluble chitin
Conductor, vinylpyrrolidone and dialkylaminoalkylmeth
Tacrylate copolymer, pyrrolidone carboxylic acid, milk
Provided is a hair cosmetic selected from shampoos, rinses and hair conditioners that does not contain acid, proline and acidic amino acids .

【0007】本発明で用いられる成分(A)の不揮発性
シリコーン類としては、不揮発性のものであれば特に制
限されず、例えばジメチルポリシロキサン、メチルフェ
ニルポリシロキサン、ポリエーテル変性シリコーン、ア
ミノ変性シリコーン、アルキル変性シリコーン、アルコ
キシ変性シリコーン等が挙げられる。
The non-volatile silicone as the component (A) used in the present invention is not particularly limited as long as it is non-volatile, and examples thereof include dimethylpolysiloxane, methylphenylpolysiloxane, polyether-modified silicone and amino-modified silicone. , Alkyl-modified silicone, alkoxy-modified silicone and the like.

【0008】これらのうち、ジメチルポリシロキサン、
メチルフェニルポリシロキサンとしては、25℃におけ
る粘度が1000cs以上、特に10万cs以上のものが、
毛髪に付着した後、容易に脱落し難いので好ましい。こ
のような高粘度のシリコーン類を使用する場合には、低
粘度(500cs以下)のジメチコーンや揮発性環状シリ
コーン、揮発性イソパラフィン等で希釈して低粘度化し
て用いてもよい。
Of these, dimethylpolysiloxane,
Methylphenyl polysiloxanes with a viscosity at 25 ° C of 1000 cs or more, especially 100,000 cs or more,
It is preferable because it does not easily come off after it adheres to the hair. When using such high viscosity silicones, they may be diluted with low viscosity (500 cs or less) dimethicone, volatile cyclic silicone, volatile isoparaffin or the like to reduce the viscosity.

【0009】また、ポリエーテル変性シリコーンとして
は、例えば次の一般式(1)〜(4)で表わされるもの
が挙げられる。
Examples of the polyether modified silicone include those represented by the following general formulas (1) to (4).

【0010】[0010]

【化1】 [Chemical 1]

【0011】(式中、R1 は炭素数1〜4のアルキル基
を示し、aは0〜35の数、bは1〜45の数、cは0
〜1000の数を示す)
(In the formula, R 1 represents an alkyl group having 1 to 4 carbon atoms, a is a number from 0 to 35, b is a number from 1 to 45, and c is 0.
~ 1000 numbers)

【0012】[0012]

【化2】 [Chemical 2]

【0013】〔式中、R2 は水素原子、炭素数1〜12
のアルキル基又は基−OCi2i(iは1〜6の数を示
す)を示し、dは2〜500(好ましくは20〜80)
の数、eは1〜50(好ましくは1〜30)の数、fは
0〜50(好ましくは1〜30)の数、gは0〜50
(好ましくは0〜35)の数、hは1〜6(好ましくは
2〜3)の数を示す〕
[In the formula, R 2 is a hydrogen atom and has 1 to 12 carbon atoms.
Indicates an alkyl group or a group -OC i H 2i (i is a number of 1 to 6), d is 2-500 (preferably 20-80)
, E is 1 to 50 (preferably 1 to 30), f is 0 to 50 (preferably 1 to 30), and g is 0 to 50.
(Preferably 0 to 35) and h represents a number of 1 to 6 (preferably 2 to 3)]

【0014】[0014]

【化3】 [Chemical 3]

【0015】〔式中、R3 はメチル基又は基−(C
2l−(OC24m−(OC36n−OHを示し、
jは1〜500(好ましくは10〜200)の数、kは
0〜100(好ましくは0〜10)の数、lは0〜6
(好ましくは2〜3)の数、mは1〜100(好ましく
は0〜10)の数、nは0〜100(好ましくは0〜2
0)の数を示す〕
[In the formula, R 3 is a methyl group or a group-(C
H 2) l - (OC 2 H 4) m - (OC 3 H 6) shows the n -OH,
j is a number of 1 to 500 (preferably 10 to 200), k is a number of 0 to 100 (preferably 0 to 10), and l is 0 to 6
(Preferably 2-3), m is 1-100 (preferably 0-10), and n is 0-100 (preferably 0-2).
0) number]

【0016】[0016]

【化4】 [Chemical 4]

【0017】〔式中、oは1〜300(好ましくは1〜
50)の数、pは0〜6(好ましくは2〜3)の数、q
は1〜50(好ましくは2〜20)の数、rは0〜50
(好ましくは0〜20)の数、sは2〜500(好まし
くは2〜50)の数を示す〕
[Wherein o is 1 to 300 (preferably 1 to 300)
50), p is a number from 0 to 6 (preferably 2 to 3), q
Is a number of 1 to 50 (preferably 2 to 20), and r is 0 to 50.
(Preferably 0 to 20) and s represents a number of 2 to 500 (preferably 2 to 50)]

【0018】アミノ変性シリコーンとしては、例えば次
の一般式(5)〜(6)で表わされるものが挙げられ
る。
Examples of the amino-modified silicone include those represented by the following general formulas (5) to (6).

【0019】[0019]

【化5】 [Chemical 5]

【0020】(式中、R4 はメチル基又はヒドロキシル
基を示し、R5 はメチル基又は水素原子を示し、R6
アルキルアミノ基又はアルケニルアミノ基を示し、R7
はヒドロキシル基、ヒドロキシアルキル基、オキシアル
キレン基又はポリオキシアルキレン基を示し、t、u及
びvはそれぞれ分子量に依存する整数を示す) これらのアミノ変性シリコーンのうち、特に次の一般式
(7)で表わされるものが好ましい。
(Wherein R 4 represents a methyl group or a hydroxyl group, R 5 represents a methyl group or a hydrogen atom, R 6 represents an alkylamino group or an alkenylamino group, and R 7
Represents a hydroxyl group, a hydroxyalkyl group, an oxyalkylene group or a polyoxyalkylene group, and t, u and v each represent an integer depending on the molecular weight.) Of these amino-modified silicones, the following general formula (7) Those represented by are preferred.

【0021】[0021]

【化6】 [Chemical 6]

【0022】(式中、R6 、u及びvは前記と同じ意味
を示す) このようなアミノ変性シリコーンの代表的なものは、次
の式(8)で表わされ、重合体の平均分子量が約3,0
00〜100,000のものであり、これはアモジメチ
コーン(Amodimethikone)の名称でCTFA辞典(米国
Cosmetic Ingredient Dictionary)第3版中に記載され
ている。
(In the formula, R 6 , u and v have the same meanings as described above.) A typical example of such an amino-modified silicone is represented by the following formula (8), and the average molecular weight of the polymer is Is about 3,0
00 to 100,000, which is the CTFA dictionary under the name of Amodimethikone (US
Cosmetic Ingredient Dictionary) 3rd edition.

【0023】[0023]

【化7】 [Chemical 7]

【0024】(式中、w及びxは分子量3,000〜1
00,000に依存する整数を示す)
(In the formula, w and x are molecular weights of 3,000 to 1)
Indicates an integer that depends on 0,000)

【0025】また、アルキル変性シリコーンとしては、
例えば次の一般式(9)〜(10)で表わされるものが
挙げられる。
As the alkyl-modified silicone,
For example, those represented by the following general formulas (9) to (10) can be mentioned.

【0026】[0026]

【化8】 [Chemical 8]

【0027】〔式中、R10は炭素数10〜20のアルキ
ル基を示し、a1 及びb1 はそれぞれ1〜1000(好
ましくは1〜200)の数を示す〕
[In the formula, R 10 represents an alkyl group having 10 to 20 carbon atoms, and a 1 and b 1 each represent a number of 1 to 1000 (preferably 1 to 200)]

【0028】更に、アルコキシ変性シリコーンとして
は、例えば次の一般式(11)で表わされるものが挙げ
られる。
Further, examples of the alkoxy-modified silicone include those represented by the following general formula (11).

【0029】[0029]

【化9】 [Chemical 9]

【0030】〔式中、R11は炭素数1〜28(好ましく
は12〜22)のアルキル基を示し、R12はメチル基又
はフェニル基を示し、c1 は0〜6の数、d1 は1〜
3,000の数、e1 及びf1 はe1 +f1 =1〜50
0となる数を示す〕 これらのアルコキシ変性シリコーンのうち、特に次の一
般式(12)で表わされるものが好ましい。
[In the formula, R 11 represents an alkyl group having 1 to 28 carbon atoms (preferably 12 to 22), R 12 represents a methyl group or a phenyl group, c 1 represents a number of 0 to 6, d 1 Is 1
The number of 3,000, e 1 and f 1 are e 1 + f 1 = 1 to 50
Among these alkoxy-modified silicones, those represented by the following general formula (12) are particularly preferable.

【0031】[0031]

【化10】 [Chemical 10]

【0032】(式中、R11は前記と同じ意味を示し、g
1 は1〜100の数、h1 は1〜50の数を示す)
(In the formula, R 11 has the same meaning as described above, and g
1 is a number from 1 to 100, h 1 is a number from 1 to 50)

【0033】成分(A)の不揮発性シリコーン類として
は、特にジメチルポリシロキサン、アミノ変性シリコー
ンが好ましい。
As the non-volatile silicones as the component (A), dimethylpolysiloxane and amino-modified silicone are particularly preferable.

【0034】不揮発性シリコーン類は、1種又は2種以
上を組合わせて用いることができ、その配合量は特に制
限されないが、全組成中に0.5〜50重量%(以下、
単に%で示す)配合するのが好ましく、特に1〜30
%、更に2〜10%配合すると、シリコーン類の毛髪で
の皮膜形成性に優れ、活性酸素ケア効果、パサツキ防止
効果等の性能をより発揮することができ、好ましい。
The non-volatile silicones may be used alone or in combination of two or more, and the compounding amount thereof is not particularly limited, but 0.5 to 50% by weight (hereinafter,
(Only shown in%) is preferable, especially 1 to 30
%, And further 2 to 10% is preferable because it is excellent in the film forming property of silicones on the hair and can exhibit the active oxygen care effect and the dryness prevention effect more effectively.

【0035】本発明で用いられる成分(B)は、ゴマ、
ブルーベリー及びハマメリスから選ばれる植物、その抽
出物又は圧搾物である。これらの植物は、その葉、根、
茎、花等をそのまま、又は細かくきざんだり、乾燥させ
て粉末状にしたり、すりつぶしたりして使用することが
できる。また、これらの植物の抽出物を得る方法として
は、例えばこれらの植物の葉、根、茎、花等を、水又は
親水性有機溶媒で抽出して抽出液を得る方法、更にこの
抽出液を乾燥させ、粉末を得る方法等が挙げられる。親
水性有機溶媒としては、例えばメタノール、エタノー
ル、1,3−ブチレングリコール、プロピレングリコー
ル等が挙げられる。これらの溶媒は単独でも、2種以上
組合わせて使用してもよく、水とこれらの溶媒を混合し
て使用してもよい。更に、ゴマはヘキサン等の有機溶媒
で抽出するか、又は圧搾することにより、ゴマ油を得る
ことができる。
The component (B) used in the present invention is sesame,
A plant selected from blueberries and hamamelis, an extract thereof or a pressed product. These plants have their leaves, roots,
The stems, flowers and the like can be used as they are, or can be finely chopped, dried to give a powder, or ground. Further, as a method of obtaining an extract of these plants, for example, leaves, roots, stems, flowers and the like of these plants are extracted with water or a hydrophilic organic solvent to obtain an extract, and this extract is further extracted. Examples thereof include a method of obtaining a powder by drying. Examples of the hydrophilic organic solvent include methanol, ethanol, 1,3-butylene glycol, propylene glycol and the like. These solvents may be used alone or in combination of two or more kinds, and water and these solvents may be mixed and used. Further, sesame oil can be obtained by extracting sesame with an organic solvent such as hexane or pressing.

【0036】このようにして得られる成分(B)のう
ち、ゴマ圧搾物、ハマメリスの抽出物が好ましい。
Among the components (B) thus obtained, sesame squeezed products and hamamelis extracts are preferred.

【0037】これらの成分(B)は、1種又は2種以上
を組合わせて用いることができる。成分(B)として植
物を用いる場合、全組成中に乾燥固形分として0.01
〜20%、特に0.1〜10%、更に0.1〜5%配合
するのが製品中安定に配合できるので好ましく、植物抽
出物を用いる場合、全組成中に乾燥固形分として0.1
〜20%、特に0.2〜10%、更に0.25〜5%配
合するのが好ましく、植物の圧搾物を用いる場合、全組
成中に乾燥固形分として0.1〜20%、特に0.1〜
10%、更に0.1〜5%配合するのが好ましい。これ
らの範囲内であると、より優れたダメージ防止効果が得
られ、しかも安定であるので好ましい。
These components (B) can be used alone or in combination of two or more. When a plant is used as the component (B), the dry solid content is 0.01% in the whole composition.
-20%, especially 0.1-10%, more preferably 0.1-5% is preferable because it can be stably mixed in the product, and when a plant extract is used, it is 0.1 as a dry solid content in the entire composition.
˜20%, especially 0.2 to 10%, more preferably 0.25 to 5% is blended, and when a pressed product of a plant is used, it is 0.1 to 20%, especially 0 as a dry solid content in the whole composition. 1 ~
It is preferable to add 10%, more preferably 0.1 to 5%. It is preferable for it to be within these ranges since a more excellent damage preventing effect is obtained and the stability is stable.

【0038】[0038]

【0039】[0039]

【0040】[0040]

【0041】[0041]

【0042】[0042]

【0043】また、本発明の毛髪化粧料には、更に紫外
線吸収剤を配合すると、紫外線防止効果が増し、活性酸
素防御能が向上し、ヘアケア効果及び安定性がより向上
するので好ましい。かかる紫外線吸収剤としては、通常
の化粧料等に用いられるものであれば特に制限されず、
例えばオクチルメトキシシンナメート、ベンゾフェノ
ン、ベンゾフェノン誘導体、パラアミノ安息香酸類、ベ
ンゾイルメタン類等が挙げられる。これらの市販品とし
ては、オクチルメトキシシンナメートとしてパーソール
MCX(ジボダン社製);ベンゾフェノン誘導体のう
ち、2−ヒドロキシ−4−メトキシベンゾフェノンとし
てUvinul M−40(BASF社製);ベンゾフ
ェノンスルホン酸としてUvinul MS−40(B
ASF社製);ベンゾフェノンスルホン酸ナトリウムと
してUvinul MS−40のナトリウム塩;パラア
ミノ安息香酸類としては、パラジメチルアミノ安息香酸
としてエスカロール507(Dan Dyk社製)、オ
クチルトリアゾンとしてUvinul T−150(B
ASF社製);ベンゾイルメタン類としては、ブチルメ
トキシジベンゾイルメタンとしてパーソール1789
(ジボダン社製)等を使用することができる。
Further, it is preferable to further add an ultraviolet absorber to the hair cosmetic composition of the present invention, because the effect of preventing ultraviolet rays is increased, the ability to protect active oxygen is improved, and the hair care effect and stability are further improved. The ultraviolet absorber is not particularly limited as long as it is used in ordinary cosmetics and the like,
Examples thereof include octyl methoxycinnamate, benzophenone, benzophenone derivatives, paraaminobenzoic acids, benzoylmethanes and the like. These commercially available products include Persole MCX (manufactured by Givaudan) as octyl methoxycinnamate; Uvinul M-40 (manufactured by BASF) as 2-hydroxy-4-methoxybenzophenone among benzophenone derivatives; Uvinul MS as benzophenone sulfonic acid. -40 (B
ASF); sodium salt of Uvinul MS-40 as sodium benzophenone sulfonate; escarol 507 (manufactured by Dan Dyk) as para-dimethylaminobenzoic acid as paraaminobenzoic acids, and Uvinul T-150 (B) as octyltriazone.
ASF Corporation); as benzoylmethanes, butylmethoxydibenzoylmethane as persol 1789
(Manufactured by Givaudan) can be used.

【0044】これらの紫外線吸収剤は、これらの紫外線
吸収効果を充分に得るために、全組成中に0.1〜20
%、特に0.2〜10%配合するのが好ましい。
These UV absorbers are contained in an amount of 0.1 to 20 in the total composition in order to obtain these UV absorbing effects sufficiently.
%, Particularly 0.2 to 10% is preferable.

【0045】本発明の毛髪化粧料には、前記成分のほ
か、目的に応じて通常の毛髪化粧料に配合される成分、
例えばカチオン界面活性剤、アニオン界面活性剤、非イ
オン界面活性剤等の界面活性剤;直鎖又は分岐鎖のアル
キル基又はアルケニル基を有する高級アルコール類;流
動パラフィン、ワセリン等の炭化水素類;液状ラノリ
ン、ラノリン脂肪酸等のラノリン誘導体;レシチン等の
リン脂質;コレステロール等のステロール及びその誘導
体;コラーゲン分解ペプチド誘導体;パーフルオロポリ
エーテル;高級アルコール高級脂肪酸エステル類、高級
脂肪酸類、アルキル基又はアルケニル基を有する長鎖ア
ミドアミン等の油脂類;ミンクオイル、オリーブ油等の
動植物油脂類;スタイリング性付与ポリマー;アルコー
ル類、プロピレングリコール等の溶剤;抗フケ剤、殺菌
剤、ビタミン類等の薬効剤;パラベン類等の防腐剤;水
溶性高分子等の増粘剤;染料及び顔料等の着色剤、収れ
ん剤、香料、色素、pH調整剤、エアゾール噴射剤等を、
本発明の効果を損なわない範囲で適宜配合することがで
きる。
The hair cosmetic composition of the present invention contains, in addition to the above-mentioned components, components that are added to ordinary hair cosmetic compositions depending on the purpose.
For example, surfactants such as cationic surfactants, anionic surfactants and nonionic surfactants; higher alcohols having a linear or branched alkyl group or alkenyl group; hydrocarbons such as liquid paraffin and vaseline; liquid Lanolin derivatives such as lanolin and lanolin fatty acids; phospholipids such as lecithin; sterols and derivatives thereof such as cholesterol; collagen-degrading peptide derivatives; perfluoropolyether; higher alcohol higher fatty acid esters, higher fatty acids, alkyl groups or alkenyl groups Oils and fats such as long-chain amidoamine; animal and vegetable oils and fats such as mink oil and olive oil; styling property imparting polymers; solvents such as alcohols and propylene glycol; antidandruff agents, bactericides, vitamins and other medicinal agents, parabens and the like Antiseptic; thickening of water-soluble polymer ; Dyes and coloring agents such as pigments, astringents, fragrances, dyes, pH adjusting agents, aerosol propellants and the like,
It can be appropriately blended within a range that does not impair the effects of the present invention.

【0046】本発明の毛髪化粧料は、前記成分を混合
し、通常の方法に従って製造することができ、シャンプ
ー、リンス又はヘアコンディショナーとすることができ
る。
The hair cosmetic composition of the present invention can be produced by mixing the above-mentioned components according to a usual method, and can be used as a shampoo, a rinse or a hair conditioner.

【0047】[0047]

【発明の効果】本発明の毛髪化粧料は、毛髪のパサツ
キ、表面の酸化、色調の変化などのダメージを防止する
ことができ、優れたヘアケア効果を有するものであり、
しかも感触が良好で、安定性及び安全性にも優れてい
る。
EFFECTS OF THE INVENTION The hair cosmetic composition of the present invention is capable of preventing damage such as dryness of the hair, surface oxidation, and change in color tone, and has an excellent hair care effect.
Moreover, it has a good feel and is excellent in stability and safety.

【0048】[0048]

【実施例】次に、実施例を挙げて本発明を更に説明する
が、本発明はこれら実施例に限定されるものではない。
なお、実施例において用いた植物抽出物等の配合量は、
乾燥固形分としての値で示した。
EXAMPLES Next, the present invention will be further described with reference to examples, but the present invention is not limited to these examples.
The amount of the plant extract or the like used in the examples is
The value is shown as a dry solid content.

【0049】[0049]

【0050】[0050]

【0051】[0051]

【0052】[0052]

【0053】[0053]

【0054】 実施例1(シャンプー組成物) (成分) (%) (1)ポリオキシエチレンラウリルエーテル硫酸Na(2EO) 12 (2)ラウリル酸ジエタノールアミド 3 (3)ジメチルポリシロキサン〔2000万cs/100cs(1/10)〕 3 (4)ブルーベリー抽出物(常盤植物化学研究所製) 0.2 (5)2−ヒドロキシ−4−メトキシベンゾフェノン (Uvinul M-40:BASF社製) 0.1 (6)エチレングリコールジステアレート 2 (7)食塩 2 (8)香料 適量 (9)色素(黄色4号) 微量 (10)防腐剤、pH調整剤 適量 (11)精製水 バランス[0054] Example 1 (shampoo composition) (Component) (%)   (1) Polyoxyethylene lauryl ether sulfate Na (2EO) 12   (2) Lauric acid diethanolamide 3   (3) Dimethylpolysiloxane [20 million cs / 100cs (1/10)] 3   (4) Blueberry extract (manufactured by Tokiwa Plant Chemistry Research Institute) 0.2   (5) 2-hydroxy-4-methoxybenzophenone         (Uvinul M-40: BASF) 0.1   (6) Ethylene glycol distearate 2   (7) Salt 2   (8) Perfume proper amount   (9) Dye (Yellow No. 4) Trace amount (10) Preservative, pH adjuster Appropriate amount (11) Purified water balance

【0055】(製法)上記成分(1)〜(11)を75
℃で均一に混合した後、冷却し、パール状のシャンプー
組成物を得た。
(Production method) 75 parts of the above components (1) to (11)
After uniformly mixing at 0 ° C, the mixture was cooled to obtain a pearly shampoo composition.

【0056】 実施例2(コンディショナー組成物) (成分) (%) (1)セトステアリルトリメチルアンモニウムクロライド 2 (2)セタノール 2 (3)ポリエーテル変性シリコーン (シリコーンKF6002:信越化学社製) 3 (4)ハマメリス抽出物 (ハマメリスリキッド:一丸ファルコス社製) 0.2 (5)オクチルトリアゾン (Uvinul T-150:BASF社製) 0.2 (6)ブチルヒドロキシトルエン 0.1 (7)ヒドロキシエチルセルロース 適量 (8)防腐剤、pH調整剤 適量 (9)香料 適量 (10)色素(緑色3号) 微量 (11)精製水 バランス[0056] Example 2 (conditioner composition) (Component) (%)   (1) cetostearyl trimethyl ammonium chloride 2   (2) Cetanol 2   (3) Polyether-modified silicone         (Silicone KF6002: manufactured by Shin-Etsu Chemical Co., Ltd.) 3   (4) Hamamelis extract         (Hamameris liquid: manufactured by Ichimaru Falcos) 0.2   (5) Octyl triazone         (Uvinul T-150: manufactured by BASF) 0.2   (6) Butylhydroxytoluene 0.1   (7) Hydroxyethyl cellulose Suitable amount   (8) Preservative, pH adjuster Appropriate amount   (9) Suitable amount of fragrance (10) Dye (Green No. 3) Trace amount (11) Purified water balance

【0057】(製法)上記成分(1)〜(11)を80
℃で均一に混合した後、冷却し、クリーム状のヘアコン
ディショナー組成物を得た。
(Production method) 80 parts of the above components (1) to (11)
After uniformly mixing at 0 ° C., the mixture was cooled to obtain a creamy hair conditioner composition.

【0058】[0058]

【0059】[0059]

【0060】[0060]

【0061】[0061]

【0062】[0062]

【0063】[0063]

【0064】実施例3(ヘアリンス剤) 以下に示す組成のヘアリンス剤を常法により製造した。Example 3 (hair rinse agent) A hair rinse agent having the composition shown below was produced by a conventional method.

【0065】[0065]

【表7】 (成分) (%) (1)セチルトリメチルアンモニウムクロリド 2.0 (2)セチルアルコール 2.5 (3)プロピレングリコール 3.0 (4)精製ゴマ油(太白ゴマ油:竹本油脂社製) 0.3 (5)ジメチルポリシロキサン〔2000万cs/100cs(1/10)〕 0.5 (6)ワセリン 0.5 (7)水 バランス 100.0[Table 7] (Components) (%) (1) Cetyltrimethylammonium chloride 2.0 (2) Cetyl alcohol 2.5 (3) Propylene glycol 3.0 (4) Purified sesame oil (thick white sesame oil: manufactured by Takemoto Yushi Co., Ltd.) 0.3 (5) Dimethyl polysiloxane [20 million cs / 100cs (1/10)] 0.5 (6) Vaseline 0.5 (7) Water balance 100.0

【0066】[0066]

【0067】[0067]

【0068】実施例1〜3で得られたシャンプー、リン
ス又はヘアコンディショナーは、いずれも紫外線による
毛髪のダメージを抑えることができ、しかも感触が良好
で、安定性及び安全性に優れたものであった。
The shampoos, rinses and hair conditioners obtained in Examples 1 to 3 are all capable of suppressing damage to the hair due to ultraviolet rays, have a good feel, and are excellent in stability and safety. It was

───────────────────────────────────────────────────── フロントページの続き (56)参考文献 特開 平5−97631(JP,A) 特開 平4−308525(JP,A) 特開 平5−170629(JP,A) 特開 平6−321742(JP,A) 特開 平5−331021(JP,A) 特開 昭57−192310(JP,A) 特開 平7−187965(JP,A) 特開 平7−196456(JP,A) 特開 平6−263620(JP,A) (58)調査した分野(Int.Cl.7,DB名) A61K 7/06 - 7/155 ─────────────────────────────────────────────────── ─── Continuation of the front page (56) Reference JP 5-97631 (JP, A) JP 4-308525 (JP, A) JP 5-170629 (JP, A) JP 6- 321742 (JP, A) JP 5-331021 (JP, A) JP 57-192310 (JP, A) JP 7-187965 (JP, A) JP 7-196456 (JP, A) JP-A-6-263620 (JP, A) (58) Fields investigated (Int.Cl. 7 , DB name) A61K 7 /06-7/155

Claims (3)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】 次の成分(A)及び(B): (A)不揮発性シリコーン類、 (B)ゴマ、ブルーベリー及びハマメリスから選ばれる
植物、その抽出物又は圧搾物を含有し、水溶性キチン誘
導体、ビニルピロリドンとジアルキルアミノアルキルメ
タクリレートの共重合体、ピロリドンカルボン酸、乳
酸、プロリン及び酸性アミノ酸を含まない、シャンプ
ー、リンス及びヘアコンディショナーから選ばれる毛髪
化粧料。
1. A water-soluble chitin containing the following components (A) and (B): (A) a non-volatile silicone, (B) a plant selected from sesame, blueberries and hamamelis, an extract or a pressed product thereof. Invitation
Conductor, vinylpyrrolidone and dialkylaminoalkylmeth
Tacrylate copolymer, pyrrolidone carboxylic acid, milk
Hair cosmetics selected from shampoos, rinses and hair conditioners that do not contain acid, proline and acidic amino acids .
【請求項2】 成分(A)の不揮発性シリコーン類が、
ジメチルポリシロキサン、メチルフェニルポリシロキサ
ン、ポリエーテル変性シリコーン、アミノ変性シリコー
ン、アルキル変性シリコーン及びアルコキシ変性シリコ
ーンから選ばれるものである請求項1記載の毛髪化粧
料。
2. The non-volatile silicones of component (A) are
The hair cosmetic composition according to claim 1, which is selected from dimethylpolysiloxane, methylphenylpolysiloxane, polyether-modified silicone, amino-modified silicone, alkyl-modified silicone and alkoxy-modified silicone.
【請求項3】 更に、オクチルメトキシシンナメート、
ベンゾフェノン、ベンゾフェノン誘導体、パラアミノ安
息香酸及びベンゾイルメタン類から選ばれる紫外線吸収
剤を含有する請求項1又は2記載の毛髪化粧料。
3. Further, octyl methoxycinnamate,
The hair cosmetic composition according to claim 1 or 2, which contains an ultraviolet absorber selected from benzophenone, benzophenone derivatives, para-aminobenzoic acid and benzoylmethanes.
JP03668295A 1995-02-24 1995-02-24 Hair cosmetics Expired - Fee Related JP3495446B2 (en)

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JP2000239144A (en) * 1999-02-22 2000-09-05 Kose Corp Langerhans cell decrease inhibitor and preparation which contain the inhibitor and is useful for external use for skin
FR2802425B1 (en) * 1999-12-21 2003-09-26 Oreal USE OF AN EXTRACT OF AT LEAST ONE PLANT FROM THE ERICACEAE FAMILY AS AN ANTI-GLYCATION AGENT
GB0014426D0 (en) * 2000-06-13 2000-08-09 Unilever Plc Hair oils
KR100360718B1 (en) * 2000-09-21 2002-11-13 주식회사 네추라 바이오 캠 Powder form Artificial-hair using natural dyes and the manufacturing method thereof
JP5344779B2 (en) * 2000-12-06 2013-11-20 花王株式会社 Hair cosmetics
KR100569788B1 (en) * 2005-07-13 2006-04-10 광덕물산주식회사 Composition for hairdye comprising mulberry, mulberry leaves or mori radicis cortex
WO2007007936A1 (en) * 2005-07-13 2007-01-18 Kwangduk Industry Co., Ltd. Composition for hairdye comprising mulberry, mulberry leaves or mori radicis cortex
JP2007161656A (en) * 2005-12-15 2007-06-28 Arimino Kagaku Kk Hair cosmetic
DE102006043767A1 (en) * 2006-09-13 2008-03-27 Henkel Kgaa Extract of Apium graveleons to stimulate hair growth
CN104546587A (en) * 2014-11-12 2015-04-29 哈尔滨灵草舒生物科技有限公司 Dandruff removing, hair growth promoting and hair blacking shampoo powder and production method thereof

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JPS57192310A (en) * 1981-05-20 1982-11-26 Kao Corp Hair dyeing agent composition
JPH05170629A (en) * 1991-02-28 1993-07-09 Lion Corp Hair dye composition
JPH0597631A (en) * 1991-03-15 1993-04-20 Sunstar Inc Hair tonic agent composition
JP2779555B2 (en) * 1991-04-05 1998-07-23 花王株式会社 Hair cosmetics
JP3082801B2 (en) * 1992-05-27 2000-08-28 ポーラ化成工業株式会社 Odor prevention method and cosmetics
JP3127658B2 (en) * 1993-03-12 2001-01-29 サンスター株式会社 Hair cosmetics
JPH06321742A (en) * 1993-05-11 1994-11-22 Kasei Kagaku Kogyo Kk Hair dressing agent composition
JPH07187965A (en) * 1993-12-28 1995-07-25 Kao Corp Hair cosmetic
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