JPH0733630A - Hair treatment composition - Google Patents

Hair treatment composition

Info

Publication number
JPH0733630A
JPH0733630A JP17808293A JP17808293A JPH0733630A JP H0733630 A JPH0733630 A JP H0733630A JP 17808293 A JP17808293 A JP 17808293A JP 17808293 A JP17808293 A JP 17808293A JP H0733630 A JPH0733630 A JP H0733630A
Authority
JP
Japan
Prior art keywords
hair
quaternary ammonium
group
carbon atoms
substituted
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.)
Pending
Application number
JP17808293A
Other languages
Japanese (ja)
Inventor
Masahiko Ogawa
真彦 小川
Michiko Asami
路子 浅見
Toru Yoshihara
徹 吉原
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
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Kao Corp filed Critical Kao Corp
Priority to JP17808293A priority Critical patent/JPH0733630A/en
Priority to DE19944425096 priority patent/DE4425096A1/en
Publication of JPH0733630A publication Critical patent/JPH0733630A/en
Pending legal-status Critical Current

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q5/00Preparations for care of the hair
    • A61Q5/10Preparations for permanently dyeing the hair
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/40Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
    • A61K8/41Amines
    • A61K8/416Quaternary ammonium compounds
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/72Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/84Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions otherwise than those involving only carbon-carbon unsaturated bonds
    • A61K8/89Polysiloxanes
    • A61K8/891Polysiloxanes saturated, e.g. dimethicone, phenyl trimethicone, C24-C28 methicone or stearyl dimethicone
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/72Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/84Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions otherwise than those involving only carbon-carbon unsaturated bonds
    • A61K8/89Polysiloxanes
    • A61K8/891Polysiloxanes saturated, e.g. dimethicone, phenyl trimethicone, C24-C28 methicone or stearyl dimethicone
    • A61K8/893Polysiloxanes saturated, e.g. dimethicone, phenyl trimethicone, C24-C28 methicone or stearyl dimethicone modified by an alkoxy or aryloxy group, e.g. behenoxy dimethicone or stearoxy dimethicone
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q5/00Preparations for care of the hair
    • A61Q5/08Preparations for bleaching the hair
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00Use of organic ingredients
    • C08K5/16Nitrogen-containing compounds
    • C08K5/17Amines; Quaternary ammonium compounds

Landscapes

  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Epidemiology (AREA)
  • Birds (AREA)
  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Cosmetics (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Abstract

(57)【要約】 【構成】 (A)融点が30℃以上のアルコキシ変性シ
リコーン誘導体、並びに25℃における粘度が1,00
0,000cs以上であるジメチルポリシロキサン及びメ
チルフェニルポリシロキサンから選ばれるシリコーン誘
導体、(B)長鎖モノアルキル型第4級アンモニウム
塩、(C)長鎖ジアルキル型第4級アンモニウム塩及び
/又は分岐アルキル型第4級アンモニウム塩、及び
(D)酸化剤を含有する毛髪処理剤。 【効果】 処理時の毛髪の損傷が防止され、毛髪に良好
な感触を付与し、経日での毛髪の色の変化を抑えること
ができる。
(57) [Summary] [Structure] (A) Alkoxy-modified silicone derivative having a melting point of 30 ° C. or higher, and a viscosity of 100 at 25 ° C.
Silicone derivative selected from dimethylpolysiloxane and methylphenylpolysiloxane of 10,000 cs or more, (B) long chain monoalkyl type quaternary ammonium salt, (C) long chain dialkyl type quaternary ammonium salt and / or branched A hair treatment agent containing an alkyl-type quaternary ammonium salt and (D) an oxidizing agent. [Effect] It is possible to prevent the hair from being damaged during the treatment, to give a good feeling to the hair, and to suppress the change in the color of the hair over time.

Description

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

【0001】[0001]

【産業上の利用分野】本発明は毛髪処理剤組成物に関
し、更に詳細には、処理時の毛髪の損傷を防止し、毛髪
に良好な感触を付与することができ、しかも経日による
色の変化を抑えることができる、ヘアブリーチ等の毛髪
処理剤組成物に関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a hair treatment composition, and more specifically, it can prevent damage to the hair during treatment, impart a good feeling to the hair, and give a color change over time. The present invention relates to a hair treatment composition such as a hair bleach that can suppress changes.

【0002】[0002]

【従来の技術及び発明が解決しようとする課題】従来、
毛髪の脱色(ブリーチ)には、過酸化水素等の酸化剤を
含有する組成物を、そのまま頭髪に適用する(1剤式)
か、又はアンモニア等のアルカリを含有する組成物と混
合して頭髪に適用する(2剤式)、いわゆるブリーチ剤
が広く使用されている。これらの毛髪処理剤は、過酸化
水素等の酸化剤を用いているため、処理時の毛髪の損傷
が著しく、従って処理後に髪のしなやかさがなくなり、
くし通りが悪くなり、洗髪等により潤い及び光沢が失わ
れ、経日で毛髪の色合いが変わってゆき、髪色が不自然
な色調になるなどの問題があった。
2. Description of the Related Art Conventionally, the problems to be solved by the invention
For hair bleaching, a composition containing an oxidizing agent such as hydrogen peroxide is applied to the hair as it is (one-agent type).
A so-called bleaching agent, which is applied to hair by mixing with a composition containing an alkali such as ammonia (two-component type), is widely used. Since these hair treatment agents use an oxidizing agent such as hydrogen peroxide, the hair is significantly damaged during the treatment, and therefore the suppleness of the hair after the treatment is eliminated,
There was a problem that the combing became poor, the moisture and gloss were lost due to washing the hair, the color of the hair changed over time, and the hair color became unnatural.

【0003】このため、アルカリ剤中にアンモニウム塩
を添加して、系のpHをさげたもの(特開昭55−855
12号)、特定の陽イオン性重合体を含有させたもの
(特開昭55−4384号)、グルコン酸等を含有させ
たもの(特開昭59−93017号)などが提案されて
いるが、いずれも十分な効果が得られるものではなかっ
た。従って、処理時の毛髪の損傷を防止し、毛髪に良好
な感触を付与でき、経日による毛髪の色の変化の少ない
毛髪処理剤が望まれていた。
Therefore, the pH of the system is lowered by adding an ammonium salt to the alkaline agent (Japanese Patent Laid-Open No. 55-855).
No. 12), those containing a specific cationic polymer (JP-A-55-4384), those containing gluconic acid and the like (JP-A-59-93017), and the like. However, none of them had sufficient effects. Therefore, there has been a demand for a hair treatment agent capable of preventing damage to the hair during treatment, imparting a good feel to the hair, and causing little change in the color of the hair over time.

【0004】[0004]

【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、酸化剤と、特定のシ
リコーン誘導体、特定の長鎖モノアルキル型第4級アン
モニウム塩、及び特定の長鎖ジアルキル型第4級アンモ
ニウム塩及び/又は分岐アルキル型第4級アンモニウム
塩とを組合わせて用いれば、処理時の毛髪の損傷を防止
し、毛髪に良好な感触を付与することができ、しかも経
日による毛髪の色の変化を抑えることができる毛髪処理
剤組成物が得られることを見出し、本発明を完成した。
Under such circumstances, the inventors of the present invention have conducted diligent research and as a result, as a result, an oxidizing agent, a specific silicone derivative, a specific long-chain monoalkyl type quaternary ammonium salt, and a specific By using a long-chain dialkyl type quaternary ammonium salt and / or a branched alkyl type quaternary ammonium salt in combination, damage to the hair during treatment can be prevented and a good feel can be imparted to the hair. Moreover, they have found that a hair treatment composition capable of suppressing the change in color of hair over time can be obtained, and completed the present invention.

【0005】すなわち、本発明は、次の成分(A)〜
(D): (A)分子中に一個又は二個以上のアルコキシ基を有
し、かつ融点が30℃以上の変性シリコーン誘導体、並
びに25℃における粘度が1,000,000cs以上で
あるジメチルポリシロキサン及びメチルフェニルポリシ
ロキサンから選ばれる一種又は二種以上のシリコーン誘
導体 (B)一般式(1)
That is, the present invention provides the following components (A) to
(D): (A) Modified silicone derivative having one or two or more alkoxy groups in the molecule and having a melting point of 30 ° C. or higher, and dimethylpolysiloxane having a viscosity at 25 ° C. of 1,000,000 cs or higher. And one or more silicone derivatives selected from and methylphenylpolysiloxane (B) General formula (1)

【0006】[0006]

【化4】 [Chemical 4]

【0007】(式中、R1 はヒドロキシル基で置換され
ていてもよい炭素数8〜22のアルキル基を示し、
2、R3 及びR4 は同一又は異なって、ヒドロキシル
基で置換されていてもよい炭素数1〜3のアルキル基又
はベンジル基を示し、Xはハロゲン原子又は炭素数1〜
2のアルキル硫酸基を示す)で表わされる長鎖モノアル
キル型第4級アンモニウム塩の一種又は二種以上 (C)一般式(2)
(In the formula, R 1 represents an alkyl group having 8 to 22 carbon atoms which may be substituted with a hydroxyl group,
R 2 , R 3 and R 4 are the same or different and each represents an alkyl group having 1 to 3 carbon atoms which may be substituted with a hydroxyl group or a benzyl group, and X is a halogen atom or 1 to 1 carbon atoms.
2 or more types of the long-chain monoalkyl type quaternary ammonium salt represented by 2) (C) General formula (2)

【0008】[0008]

【化5】 [Chemical 5]

【0009】(式中、R5 及びR6 は同一又は異なっ
て、ヒドロキシル基で置換されていてもよい炭素数8〜
22のアルキル基を示し、R7 及びR8 は同一又は異な
って、ヒドロキシル基で置換されていてもよい炭素数1
〜3のアルキル基を示し、Xは前記と同じ意味を示す)
で表わされる長鎖ジアルキル型第4級アンモニウム塩及
び一般式(3)
(In the formula, R 5 and R 6 are the same or different and have 8 to 8 carbon atoms which may be substituted with a hydroxyl group.
22 represents an alkyl group, wherein R 7 and R 8 are the same or different and have 1 carbon atom which may be substituted with a hydroxyl group.
To 3 alkyl groups, and X has the same meaning as above.)
A long-chain dialkyl-type quaternary ammonium salt represented by the general formula (3)

【0010】[0010]

【化6】 [Chemical 6]

【0011】で表わされる分岐アルキル型第4級アンモ
ニウム塩から選ばれる一種又は二種以上 (D)酸化剤 を含有する毛髪処理剤組成物を提供するものである。
The present invention provides a hair treatment composition containing one or more selected from branched alkyl quaternary ammonium salts represented by (D) an oxidizing agent.

【0012】本発明で用いられる(A)成分のシリコー
ン誘導体のうち、アルコキシ変性シリコーン誘導体は、
融点が30℃以上(常温(25℃)で固体)の1分子中
に一個又は二個以上のアルコキシ基を有するシロキサン
ポリマーであり、その分子形態は直鎖状、分岐鎖状又は
網状のいずれであってもよい。アルコキシ変性シリコー
ン誘導体を形成するオルガノシロキサン中には、アルコ
キシ基以外にメチル基、エチル基、プロピル基などのア
ルキル基;ビニル基、アリル基などのアルケニル基;フ
ェニル基、ナフチル基などのアリール基;シクロヘキシ
ル基などのシクロアルキル基などの官能基が含まれてい
てもよい。メチル基を含むものが一般的に用いられる。
Among the silicone derivatives of the component (A) used in the present invention, the alkoxy-modified silicone derivative is
It is a siloxane polymer having one or two or more alkoxy groups in one molecule having a melting point of 30 ° C. or higher (solid at room temperature (25 ° C.)), and its molecular form may be linear, branched or reticulated. It may be. In the organosiloxane forming the alkoxy-modified silicone derivative, in addition to the alkoxy group, an alkyl group such as a methyl group, an ethyl group and a propyl group; an alkenyl group such as a vinyl group and an allyl group; an aryl group such as a phenyl group and a naphthyl group; Functional groups such as cycloalkyl groups such as cyclohexyl groups may be included. Those containing a methyl group are generally used.

【0013】上記変性シリコーン誘導体に含まれるアル
コキシ基の代表的な例は次の一般式(4)で示される。
A typical example of the alkoxy group contained in the modified silicone derivative is represented by the following general formula (4).

【化7】−(CH2) kO−R14 (4) (式中、R14は炭素数1〜28(好ましくは炭素数12
〜22)のアルキル基を表わし、kは0〜6の整数を表
わす)
Embedded image — (CH 2 ) k O—R 14 (4) (wherein R 14 has 1 to 28 carbon atoms (preferably 12 carbon atoms).
To 22), and k represents an integer of 0 to 6).

【0014】アルコキシ変性シリコーン誘導体の代表的
なものは次の一般式(5)で表わされる。
A typical alkoxy-modified silicone derivative is represented by the following general formula (5).

【0015】[0015]

【化8】 [Chemical 8]

【0016】(式中、R15はメチル基又はフェニル基を
表わし、lは1〜3000の整数を表わし、m及びp
は、m+p=1〜500となる整数を表わし、R14及び
kは前記と同じ意味であるが、これらは、それぞれ同一
又は異なっていてもよい)
(In the formula, R 15 represents a methyl group or a phenyl group, l represents an integer of 1 to 3000, and m and p
Represents an integer such that m + p = 1 to 500, and R 14 and k have the same meanings as described above, but they may be the same or different.

【0017】上記式(5)で表わされるアルコキシ変性
シリコーン誘導体のうち、特に好ましいものとしては次
の一般式(6)で表わされるものが挙げられる。
Among the alkoxy-modified silicone derivatives represented by the above formula (5), particularly preferable ones include those represented by the following general formula (6).

【0018】[0018]

【化9】 [Chemical 9]

【0019】(式中、l′は1〜100の整数を表わ
し、m′は1〜50の整数を表わし、R 14は前記と同じ
意味である)
(In the formula, l'represents an integer of 1 to 100.
M ′ represents an integer of 1 to 50, and R 14Is the same as above
Meaning)

【0020】これらのアルコキシ変性シリコーン誘導体
の融点は30℃以上60℃以下で、特に40℃以上50
℃以下であるのが好ましい。具体例としては、一般式
(6)において、ステアロキシ変性シリコーンとしては
l′=5〜30、m′=2〜15、好ましくはl′=7
〜13、m′=2〜8のもの、セチロキシ変性シリコー
ンとしてはl′=5〜30、m′=2〜15、好ましく
はl′=7〜13、m′=2〜8のもの、ミリスチロキ
シ変性シリコーンとしてはl′=5〜30、m′=2〜
15、好ましくはl′=6〜10、m′=3〜9のもの
が挙げられる。これらの変性シリコーン誘導体は高級ア
ルコール等の油脂類と相溶性がよく、これを配合すると
乳化物の保存安定性が向上する。また固体状であること
から染色した毛髪のべたつきがなく、水分閉塞性に優れ
ている。
The melting point of these alkoxy-modified silicone derivatives is from 30 ° C to 60 ° C, especially from 40 ° C to 50 ° C.
It is preferably at most ° C. As a specific example, in the general formula (6), the stearoxy-modified silicone has l '= 5 to 30, m' = 2 to 15, and preferably l '= 7.
~ 13, m '= 2-8, as cetoxy modified silicone 1' = 5-30, m '= 2-15, preferably 1' = 7-13, m '= 2-8, myristyloxy As modified silicone, l '= 5-30, m' = 2-
15, preferably 1 '= 6 to 10 and m' = 3 to 9. These modified silicone derivatives have good compatibility with fats and oils such as higher alcohols, and when they are blended, the storage stability of the emulsion is improved. In addition, since it is solid, the dyed hair does not have stickiness and has excellent water-occluding properties.

【0021】また、本発明に用いられる(A)成分のも
う一方の成分は25℃における粘度が1,000,00
0cs以上であるジメチルポリシロキサン、メチルフェニ
ルポリシロキサンである。これらのシリコーン誘導体
は、25℃における粘度が1,000,000cs以上で
あることが必要であるが、3,000,000cs以上、
特に5,000,000〜50,000,000csの範
囲が好ましい。粘度が1,000,000cs未満では効
果の持続性が十分でない。なお、ここで用いられる粘度
は、化粧品原料基準第2版試験法、粘度測定法第2法に
より、25℃において、ブルックフィールド回転粘度計
を用いて測定した値である。
The other component of the component (A) used in the present invention has a viscosity at 25 ° C. of 1,000,000.
Dimethyl polysiloxane and methyl phenyl polysiloxane with 0 cs or more. These silicone derivatives are required to have a viscosity at 25 ° C. of 1,000,000 cs or more,
Particularly, the range of 5,000,000 to 50,000,000 cs is preferable. If the viscosity is less than 1,000,000 cs, the effect persistence is not sufficient. The viscosity used here is a value measured by a Brookfield rotational viscometer at 25 ° C. according to the cosmetic raw material standard second edition test method and viscosity measurement method second method.

【0022】これらのシリコーン誘導体は一種又は二種
以上を組合わせて用いることができ、全組成中に0.1
〜25重量%(以下、単に%で示す)、特に0.1〜1
0%、更に0.2〜5%配合するのが、べたつきがなく
好ましい。
These silicone derivatives may be used either individually or in combination of two or more, and may be 0.1
-25% by weight (hereinafter referred to simply as%), especially 0.1-1
It is preferable to add 0%, and further 0.2 to 5%, since there is no stickiness.

【0023】(B)成分の長鎖モノアルキル型第4級ア
ンモニウム塩は前記一般式(1)で表わされるものであ
り、具体例としては、塩化ラウリルトリメチルアンモニ
ウム、臭化ラウリルトリメチルアンモニウム、塩化ミリ
スチルトリメチルアンモニウム、臭化ミリスチルトリメ
チルアンモニウム、塩化セチルトリメチルアンモニウ
ム、臭化セチルトリメチルアンモニウム、塩化ステアリ
ルトリメチルアンモニウム、臭化ステアリルトリメチル
アンモニウム、塩化ベヘニルトリメチルアンモニウム、
臭化ベヘニルトリメチルアンモニウム、セチルトリメチ
ルアンモニウムメタンスルホネート、ステアリルトリメ
チルアンモニウムメタンスルホネート、塩化ミリスチル
ジメチルベンジルアンモニウム、塩化セチルジメチルベ
ンジルアンモニウム、塩化ステアリルジメチルベンジル
アンモニウム、塩化オクチルジヒドロキシエチルメチル
アンモニウム等が挙げられる。
The long-chain monoalkyl type quaternary ammonium salt as the component (B) is represented by the above general formula (1), and specific examples thereof include lauryl trimethyl ammonium chloride, lauryl trimethyl ammonium bromide and myristyl chloride. Trimethylammonium, myristyltrimethylammonium bromide, cetyltrimethylammonium chloride, cetyltrimethylammonium bromide, stearyltrimethylammonium chloride, stearyltrimethylammonium bromide, behenyltrimethylammonium chloride,
Examples thereof include behenyltrimethylammonium bromide, cetyltrimethylammonium methanesulfonate, stearyltrimethylammonium methanesulfonate, myristyldimethylbenzylammonium chloride, cetyldimethylbenzylammonium chloride, stearyldimethylbenzylammonium chloride and octyldihydroxyethylmethylammonium chloride.

【0024】(B)成分は一種又は二種以上を組合わせ
て用いることができ、全組成中に0.05〜10%、特
に0.2〜8%配合すると、洗浄により簡単に脱落しな
いので好ましい。
The component (B) can be used alone or in combination of two or more. If it is added in an amount of 0.05 to 10%, especially 0.2 to 8% in the total composition, it will not easily fall off by washing. preferable.

【0025】(C)成分のうち、長鎖ジアルキル型第4
級アンモニウム塩は前記一般式(2)で表わされるもの
であり、具体例としては、塩化ジステアリルジメチルア
ンモニウム、塩化ジセチルジメチルアンモニウム、塩化
ジココイルジメチルアンモニウム、塩化ジアルキル(C
12〜C15)ジメチルアンモニウム、塩化ジアルキル(C
14〜C18)ジメチルアンモニウム等が挙げられる。
Of the component (C), the long-chain dialkyl type fourth
The primary ammonium salt is represented by the general formula (2), and specific examples thereof include distearyldimethylammonium chloride, dicetyldimethylammonium chloride, dicocoyldimethylammonium chloride and dialkyl (C
12 -C 15) dimethyl ammonium, dialkyl chloride (C
14- C18 ) dimethylammonium etc. are mentioned.

【0026】また、分岐アルキル型第4級アンモニウム
塩は前記一般式(3)で表わされるものであり、具体例
としては、塩化2−デシルテトラデシルトリメチルアン
モニウム、塩化2−ドデシルヘキサデシルトリメチルア
ンモニウム、塩化ジ(2−ヘキシルデシル)ジメチルア
ンモニウム、塩化ジ(2−オクチルドデシル)ジメチル
アンモニウム等が挙げられる。これらの分岐アルキル型
第4級アンモニウム塩は、通常、炭素数8〜36のゲル
ベアルコール
The branched alkyl quaternary ammonium salt is represented by the general formula (3), and specific examples thereof include 2-decyltetradecyltrimethylammonium chloride, 2-dodecylhexadecyltrimethylammonium chloride, Examples thereof include di (2-hexyldecyl) dimethylammonium chloride and di (2-octyldodecyl) dimethylammonium chloride. These branched alkyl quaternary ammonium salts are usually Guerbet alcohols having 8 to 36 carbon atoms.

【0027】[0027]

【化10】 [Chemical 10]

【0028】を原料として合成され、かかるゲルベアル
コールとしては、例えば2−ヘキシルデカノール、2−
オクチルドデカノール、2−デシルテトラデシルアルコ
ール、2−ドデシルヘキサデシルアルコール等が挙げら
れる。
Examples of such Guerbet alcohols synthesized by using as raw materials include 2-hexyldecanol and 2-hexyldecanol.
Octyl dodecanol, 2-decyl tetradecyl alcohol, 2-dodecyl hexadecyl alcohol and the like can be mentioned.

【0029】これらの長鎖ジアルキル型第4級アンモニ
ウム塩、分岐アルキル型第4級アンモニウム塩は一種又
は二種以上を組合わせて用いることができ、全組成中に
0.01〜10%、特に0.1〜5%配合すると、洗浄
により簡単に脱落しないので好ましい。
These long-chain dialkyl-type quaternary ammonium salts and branched alkyl-type quaternary ammonium salts can be used alone or in combination of two or more, and 0.01 to 10% in the total composition, particularly A content of 0.1 to 5% is preferable because it is not easily removed by washing.

【0030】(D)成分の酸化剤としては、例えば過酸
化水素、過硫酸アンモニウム、過硫酸カリウム等の過硫
酸塩、過ホウ酸塩、過炭酸塩、臭素酸塩等が挙げられ、
特に過酸化水素が好ましい。これらの酸化剤は一種又は
二種以上を組合わせて用いることができ、全組成中に
0.5〜10%、特に1〜8%配合すると、頭皮等への
刺激が強くならず好ましい。
Examples of the oxidizing agent as the component (D) include hydrogen peroxide, persulfates such as ammonium persulfate and potassium persulfate, perborates, percarbonates and bromates.
Hydrogen peroxide is particularly preferable. These oxidants can be used alone or in combination of two or more, and if they are added in an amount of 0.5 to 10%, especially 1 to 8% in the total composition, irritation to the scalp and the like is not strong, which is preferable.

【0031】本発明の毛髪処理剤組成物には、前記必須
成分のほか、通常の化粧料に用いられる成分、例えば乳
化剤、可溶化剤、増粘剤、安定化剤、整髪基剤、香料等
を添加することができる。ここで用いられる乳化剤とし
ては、例えば脂肪酸アルカノールアミド、エチレンオキ
サイドと脂肪アルコールとの付加生成物、ポリオキシエ
チレンノニルフェニルエーテル等が挙げられ、増粘剤と
しては、例えばメチルセルロース、ヒドロキシエチルセ
ルロース、天然水溶性高分子(デンプン、カラギーナ
ン、ローカストビーンガム、キサンタンガム、グアーガ
ムなど)等が挙げられる。安定化剤としては、例えば亜
硫酸ナトリウム等の酸化防止剤、キレート剤、紫外線吸
収剤等が挙げられ、整髪基剤としては、例えば高級アル
コール、脂肪酸エステル、非イオン性界面活性剤等の油
剤、各種のカチオンポリマー等が挙げられる。更に本発
明の毛髪処理剤組成物には、(A)成分以外のシリコー
ン誘導体、例えば環状シリコーン、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
ーン等を配合することができ、感触を向上させることが
できる。
In the hair treatment composition of the present invention, in addition to the above-mentioned essential components, components used in ordinary cosmetics such as emulsifiers, solubilizers, thickeners, stabilizers, hair styling bases, fragrances, etc. Can be added. Examples of emulsifiers used here include fatty acid alkanolamides, addition products of ethylene oxide and fatty alcohols, and polyoxyethylene nonylphenyl ether. Examples of thickeners include methyl cellulose, hydroxyethyl cellulose, and natural water-soluble agents. Polymers (starch, carrageenan, locust bean gum, xanthan gum, guar gum, etc.) and the like can be mentioned. Examples of the stabilizer include antioxidants such as sodium sulfite, chelating agents, and ultraviolet absorbers. Examples of the hair styling base include oils such as higher alcohols, fatty acid esters, and nonionic surfactants, and various types. And the cationic polymer. Further, the hair treatment composition of the present invention may contain a silicone derivative other than the component (A), for example, cyclic silicone, polyether-modified silicone, amino-modified silicone, alkyl-modified silicone, etc. to improve the feel. You can

【0032】本発明の毛髪処理剤組成物は、通常の方法
により製造することができ、クリーム、エマルジョン、
乳液、クイックブレーキング・フォーム(QBF)等の
剤型とすることができる。また、1剤式又は2剤式のヘ
アブリーチ剤、酸化染毛剤の第2剤、脱染剤の第2剤等
に適用することができる。
The hair treatment composition of the present invention can be produced by a conventional method, such as creams, emulsions,
Formulations such as emulsion and quick breaking foam (QBF) can be used. Further, it can be applied to a one-component or two-component hair bleaching agent, a second agent of an oxidative hair dye, a second agent of a decolorizing agent, and the like.

【0033】本発明の毛髪処理剤組成物を用いて毛髪を
処理するには、1剤式の場合、例えばシャンプー後に、
本発明の毛髪処理剤を頭髪に適用し、3〜5分放置後に
すすげばよく、また、2剤式の場合、例えば本発明の毛
髪処理剤(第2剤)とアルカリ剤を含有する組成物(第
1剤)を混合し、この混合液を頭髪に適用し、10〜3
0分放置後に洗い流せばよい。なお、本発明の毛髪処理
剤は通常、15〜40℃で適用するのが好ましい。
To treat hair using the hair treatment composition of the present invention, in the case of a one-component type, for example, after shampooing,
It is sufficient to apply the hair treatment agent of the present invention to hair and leave it for 3 to 5 minutes before rinsing. In the case of a two-part type, for example, a composition containing the hair treatment agent (second agent) of the present invention and an alkaline agent. (1st agent) is mixed, and this mixed solution is applied to the hair.
Rinse after leaving for 0 minutes. The hair treatment agent of the present invention is usually preferably applied at 15 to 40 ° C.

【0034】[0034]

【発明の効果】本発明の毛髪処理剤組成物は、処理時の
毛髪の損傷を防止し、毛髪に良好な感触を付与すること
ができ、しかも経日での毛髪の色の変化を抑えることが
できるものである。
EFFECTS OF THE INVENTION The hair treatment composition of the present invention can prevent damage to the hair during treatment, impart a good feel to the hair, and suppress the change in color of the hair over time. Is something that can be done.

【0035】[0035]

【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。
EXAMPLES Next, the present invention will be further described with reference to examples, but the present invention is not limited to these examples.

【0036】実施例1 表3に示す組成のクリーム状ブリーチ剤第1剤、及び表
4に示す組成のブリーチ剤第2剤を製造し、その性能に
ついて評価した。結果を表5に示す。 (製造法) 第1剤:プロピレングリコール中に、塩化ベヘニルトリ
メチルアンモニウム、流動パラフィン及びセトステアリ
ルアルコールを加熱溶解し、70℃で水と溶解した。4
0℃まで放冷した後、強アンモニア水を加え、ブリーチ
剤第1剤を得た。 第2剤:水にフェナセチンを加熱溶解し、別途プロピレ
ングリコール中で加熱溶解した油相を約70℃で混合し
た。40℃まで放冷した後、ジメチルポリシロキサン、
過酸化水素を添加し、リン酸でpHを調整して、ブリーチ
剤第2剤を得た。
Example 1 A cream-type bleaching agent No. 1 having the composition shown in Table 3 and a bleaching agent No. 2 agent having the composition shown in Table 4 were produced and their performances were evaluated. The results are shown in Table 5. (Production method) First agent: Behenyltrimethylammonium chloride, liquid paraffin and cetostearyl alcohol were dissolved by heating in propylene glycol, and dissolved at 70 ° C with water. Four
After cooling to 0 ° C., strong ammonia water was added to obtain a first bleaching agent. Second agent: Phenacetin was dissolved in water by heating, and an oil phase separately heated and dissolved in propylene glycol was mixed at about 70 ° C. After cooling to 40 ° C, dimethylpolysiloxane,
Hydrogen peroxide was added and the pH was adjusted with phosphoric acid to obtain a second bleaching agent.

【0037】(評価方法)第1剤に第2剤を等量加えて
混合した。これを黒髪トレスに塗布し、30℃で30分
間放置した後、すすぎ、シャンプー及びリンスを行い、
乾燥した。その結果、それぞれの黒髪トレスとも、十分
に脱色された。次にこれらについてのブリーチ直後の評
価、洗髪後の評価を以下の基準に従って行った。
(Evaluation Method) An equal amount of the second agent was added to the first agent and mixed. Apply this to black hair tress and leave at 30 ° C for 30 minutes, then rinse, shampoo and rinse,
Dried. As a result, each black hair tress was sufficiently decolorized. Next, the evaluation immediately after bleaching and the evaluation after washing hair were performed according to the following criteria.

【0038】[0038]

【表1】 (1)ブリーチ直後の評価 (毛髪の感触) ○:しなやかでくし通りが良い △:ややしなやかさ、くし通りが劣る ×:しなやかさがなく、くし通りが劣る (毛髪の損傷)ブリーチ前後での毛髪の表面を走査型電
子顕微鏡(3000倍)で観察し、毛小皮の損傷の程度
を下記基準により評価した。 ○:ブリーチ前と同じで、損傷が認められない △:毛小皮にわずかに隆起、亀裂、剥離等の損傷が認め
られる ×:毛小皮にかなりの隆起、亀裂、剥離等の損傷が認め
られる
[Table 1] (1) Evaluation immediately after bleaching (feeling of hair) ◯: Supple and good combability Δ: Slightly supple and poor combability X: No suppleness and poor combability (damage to hair) The surface of the hair before and after bleaching was observed with a scanning electron microscope (3000 times), and the degree of damage to the hair scalp was evaluated according to the following criteria. ◯: Same as before bleaching, no damage is observed Δ: Slight bumps, cracks, peeling or other damage is observed on the hair follicles ×: Significant bumps, cracks, peeling or other damage is found on the hair follicles To be

【0039】(2)洗髪後の評価 上記ブリーチトレスを、市販のシャンプーで洗浄及び乾
燥するプロセスを4回繰り返して行い、当該処理を行わ
ないブリーチトレスと比較して、下記の評価を行った。
(2) Evaluation after washing hair The above bleaching tress was subjected to a process of washing and drying with a commercially available shampoo four times, and the following evaluations were made in comparison with the bleaching tress not treated.

【表2】 (色調) ○:色調の変化が認められない ×:色調がやや赤茶けてきている (毛髪の感触) ○:シャンプー処理を行わなかったブリーチトレスとの
差が認められない △:シャンプー処理を行わなかったブリーチトレスとく
らべ、ややしなやかさ、くし通りが劣る ×:シャンプー処理を行わなかったブリーチトレスとく
らべ、かなりしなやかさ、くし通りが劣る (毛髪の損傷:走査型電子顕微鏡(3000倍)での観
察) ○:シャンプー処理を行わなかったブリーチトレスとの
差が認められない △:シャンプー処理を行わなかったブリーチトレスとく
らべ、毛小皮にわずかに隆起、亀裂、剥離等の損傷が認
められる ×:シャンプー処理を行わなかったブリーチトレスとく
らべ、毛小皮にかなりの隆起、亀裂、剥離等の損傷が認
められる
[Table 2] (Color tone) ○: No change in color tone is observed ×: Color tone is slightly reddish brown (feeling of hair) ○: No difference from bleach tress without shampoo treatment Δ: Shampoo Inferior in suppleness and combability compared to untreated bleach tress. ×: Compared to unbleached bleachtress in which shampoo was not applied, considerably less supple and combability (hair damage: scanning electron microscope (3000 ×) Observation: ○: No difference from bleach tress not treated with shampoo △: Compared with bleach tress not treated with shampoo, slight bulge, crack, peeling, etc. damage to hair scalp X: Compared to bleach tress without shampoo treatment, damage such as considerable bumps, cracks, and peeling was observed on the hair follicles. That

【0040】[0040]

【表3】 [Table 3]

【0041】[0041]

【表4】 [Table 4]

【0042】[0042]

【表5】 [Table 5]

【0043】実施例2 下記組成の1剤式ヘアブリーチ剤を常法により製造し
た。
Example 2 A one-part hair bleaching agent having the following composition was produced by a conventional method.

【表6】 (成分) (%) 塩化ステアリルトリメチルアンモニウム 2.30 塩化ジステアリルジメチルアンモニウム 0.40 塩化ジアルキルジメチルアンモニウム(12〜15) 0.40 セトステアリルアルコール 5.00 グリセリン 3.00 メチルパラベン 0.10 ジメチルポリシロキサン(14,000,000cs) 1.00 ジメチルポリシロキサン(500cs) 3.00 フェナセチン 0.10 過酸化水素(35%) 7.50 リン酸 pH3調整量 水 バランス(Table 6) (Components) (%) Stearyl trimethyl ammonium chloride 2.30 Distearyl dimethyl ammonium chloride 0.40 Dialkyl dimethyl ammonium chloride (12-15) 0.40 Cetostearyl alcohol 5.00 Glycerin 3.00 Methyl paraben 0. 10 Dimethylpolysiloxane (14,000,000cs) 1.00 Dimethylpolysiloxane (500cs) 3.00 Phenacetin 0.10 Hydrogen peroxide (35%) 7.50 Phosphoric acid pH3 adjustment amount Water balance

【0044】黒髪トレスをシャンプーし、タオルドライ
した後、得られたヘアブリーチ剤を10g塗布し、30
℃で5分放置し、その後流水ですすいで乾燥させた。こ
のプロセスを5回繰り返すと、黒髪トレスはやや栗色に
変化した。この状態でのトレスはしなやかでくし通りも
良く、走査型電子顕微鏡での状態観察でも損傷は認めら
れなかった。このトレスを本発明品を用いずに更にシャ
ンプー処理を5回繰り返した。この状態でのトレスもし
なやかさを失ってはいず、色調の変化もなく、走査型電
子顕微鏡での状態観察でも損傷は認められなかった。
After shampooing the black hair tress and towel-drying, 10 g of the obtained hair bleaching agent was applied, and 30
It was left at ℃ for 5 minutes, then rinsed with running water and dried. When this process was repeated 5 times, the black hair tress turned a little maroon. In this state, the tress was supple and combed well, and no damage was observed by observing the state with a scanning electron microscope. This tress was further shampooed 5 times without using the product of the present invention. The tress in this state did not lose its suppleness, there was no change in color tone, and no damage was observed by observing the state with a scanning electron microscope.

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】 次の成分(A)〜(D): (A)分子中に一個又は二個以上のアルコキシ基を有
し、かつ融点が30℃以上の変性シリコーン誘導体、並
びに25℃における粘度が1,000,000cs以上で
あるジメチルポリシロキサン及びメチルフェニルポリシ
ロキサンから選ばれる一種又は二種以上のシリコーン誘
導体 (B)一般式(1) 【化1】 (式中、R1 はヒドロキシル基で置換されていてもよい
炭素数8〜22のアルキル基を示し、R2、R3 及びR
4 は同一又は異なって、ヒドロキシル基で置換されてい
てもよい炭素数1〜3のアルキル基又はベンジル基を示
し、Xはハロゲン原子又は炭素数1〜2のアルキル硫酸
基を示す)で表わされる長鎖モノアルキル型第4級アン
モニウム塩の一種又は二種以上 (C)一般式(2) 【化2】 (式中、R5 及びR6 は同一又は異なって、ヒドロキシ
ル基で置換されていてもよい炭素数8〜22のアルキル
基を示し、R7 及びR8 は同一又は異なって、ヒドロキ
シル基で置換されていてもよい炭素数1〜3のアルキル
基を示し、Xは前記と同じ意味を示す)で表わされる長
鎖ジアルキル型第4級アンモニウム塩及び一般式(3) 【化3】 で表わされる分岐アルキル型第4級アンモニウム塩から
選ばれる一種又は二種以上 (D)酸化剤 を含有する毛髪処理剤組成物。
1. The following components (A) to (D): (A) A modified silicone derivative having one or more alkoxy groups in the molecule and having a melting point of 30 ° C. or higher, and a viscosity at 25 ° C. One or more kinds of silicone derivatives selected from dimethylpolysiloxane and methylphenylpolysiloxane having 1,000,000 or more (B) General formula (1) (In the formula, R 1 represents an alkyl group having 8 to 22 carbon atoms which may be substituted with a hydroxyl group, and R 2 , R 3 and R
4 are the same or different and each represents an alkyl group having 1 to 3 carbon atoms or a benzyl group which may be substituted with a hydroxyl group, and X represents a halogen atom or an alkyl sulfate group having 1 to 2 carbon atoms). One or more long chain monoalkyl type quaternary ammonium salts (C) General formula (2) (In the formula, R 5 and R 6 are the same or different and represent an alkyl group having 8 to 22 carbon atoms which may be substituted with a hydroxyl group, and R 7 and R 8 are the same or different and are substituted with a hydroxyl group. A long-chain dialkyl-type quaternary ammonium salt represented by the formula (3), which represents an alkyl group having 1 to 3 carbon atoms and X has the same meaning as described above, and a compound represented by the general formula (3): A hair treatment composition containing one or more selected from the branched alkyl quaternary ammonium salts represented by (D) an oxidizing agent.
JP17808293A 1993-07-19 1993-07-19 Hair treatment composition Pending JPH0733630A (en)

Priority Applications (2)

Application Number Priority Date Filing Date Title
JP17808293A JPH0733630A (en) 1993-07-19 1993-07-19 Hair treatment composition
DE19944425096 DE4425096A1 (en) 1993-07-19 1994-07-15 Hair treatment compositions

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP17808293A JPH0733630A (en) 1993-07-19 1993-07-19 Hair treatment composition

Publications (1)

Publication Number Publication Date
JPH0733630A true JPH0733630A (en) 1995-02-03

Family

ID=16042316

Family Applications (1)

Application Number Title Priority Date Filing Date
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Country Status (2)

Country Link
JP (1) JPH0733630A (en)
DE (1) DE4425096A1 (en)

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH11193224A (en) * 1997-12-26 1999-07-21 Kao Corp Oxidizing agent composition for dyeing and bleaching hair
JP2003081791A (en) * 2001-09-14 2003-03-19 Hoyu Co Ltd Oxidizer composition, and hair color or hair decolorant
JP2003081790A (en) * 2001-09-13 2003-03-19 Hoyu Co Ltd Decolorant composition and hair color composition
JP2004091356A (en) * 2002-08-30 2004-03-25 Kanebo Ltd Simultaneously spraying type creamy hair dye composition
JP2007008860A (en) * 2005-06-30 2007-01-18 Milbon Co Ltd Hair treatment agent
JP2011093822A (en) * 2009-10-27 2011-05-12 Hoyu Co Ltd Hair cosmetic composition, method for using the same, and hair cosmetic article

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ATE195650T1 (en) * 1994-05-27 2000-09-15 Goldwell Gmbh USE OF POLYORGANOSILOXANES IN BLONDERING PRODUCTS FOR HUMAN HAIR
AUPN499895A0 (en) * 1995-08-23 1995-09-14 Procter & Gamble Company, The Hair treatment composition
TW527191B (en) * 1997-07-09 2003-04-11 Kao Corp Hair treatment composition
US6149899A (en) * 1998-08-07 2000-11-21 Helene Curtis, Inc. Opaque conditioning composition
MXPA01001414A (en) * 1998-08-07 2002-11-29 Unilever Nv Opaque conditioning composition.
GB2470208B (en) 2009-05-14 2014-01-29 Thornton & Ross Ltd A method and composition for the control of ectoparasites

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH11193224A (en) * 1997-12-26 1999-07-21 Kao Corp Oxidizing agent composition for dyeing and bleaching hair
JP2003081790A (en) * 2001-09-13 2003-03-19 Hoyu Co Ltd Decolorant composition and hair color composition
JP2003081791A (en) * 2001-09-14 2003-03-19 Hoyu Co Ltd Oxidizer composition, and hair color or hair decolorant
JP2004091356A (en) * 2002-08-30 2004-03-25 Kanebo Ltd Simultaneously spraying type creamy hair dye composition
JP2007008860A (en) * 2005-06-30 2007-01-18 Milbon Co Ltd Hair treatment agent
JP2011093822A (en) * 2009-10-27 2011-05-12 Hoyu Co Ltd Hair cosmetic composition, method for using the same, and hair cosmetic article

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Publication number Publication date
DE4425096A1 (en) 1995-01-26

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