JPS6272607A - Hair rinse agent composition - Google Patents

Hair rinse agent composition

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Publication number
JPS6272607A
JPS6272607A JP21196985A JP21196985A JPS6272607A JP S6272607 A JPS6272607 A JP S6272607A JP 21196985 A JP21196985 A JP 21196985A JP 21196985 A JP21196985 A JP 21196985A JP S6272607 A JPS6272607 A JP S6272607A
Authority
JP
Japan
Prior art keywords
hair
formula
quaternary ammonium
fatty acid
carbon atoms
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
Application number
JP21196985A
Other languages
Japanese (ja)
Other versions
JPH0236566B2 (en
Inventor
Yoshiaki Abe
吉明 阿部
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 JP21196985A priority Critical patent/JPS6272607A/en
Publication of JPS6272607A publication Critical patent/JPS6272607A/en
Publication of JPH0236566B2 publication Critical patent/JPH0236566B2/ja
Granted legal-status Critical Current

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Abstract

PURPOSE:A hair rinse agent composition showing improved rinsing effect even in a dried state and imparting beautiful luster to the hair, using a specific branched fatty acid cholesteryl ester as a rinse base and comprising a quaternary ammonium salt as the main component. CONSTITUTION:A hair rinse composition containing 0.1-10wt% quaternary ammonium salt, preferably a quaternary ammonium salt (e.g., stearyltrimethylammonium chloride, etc.,) shown by the formula I (R1-R4 are alkyl or hydroxyalkyl; X is halogen or alkyl sulfate) and 0.1-10wt% branched fatty acid cholesteryl ester [e.g., 5,7,7-trimethyl-2-(1,3,3-trimethylbutyl)-octanoic acid, etc.,] shown by the formula II (R has 11-23 total carbon atoms and saturated aliphatic hydrocarbon containing alkyl group between a carboxyl bond position and the center of main chain).

Description

【発明の詳細な説明】 〔産業上の利用分野〕 本発明は新規なヘアリンス剤組成物、更に詳細には、特
定の分岐脂肪酸コレステリルエステルを含有するヘアリ
ンス剤組成物に関する。
DETAILED DESCRIPTION OF THE INVENTION [Industrial Field of Application] The present invention relates to a novel hair rinse composition, and more particularly to a hair rinse composition containing a specific branched fatty acid cholesteryl ester.

〔従来の技術及びその問題点〕[Conventional technology and its problems]

従来、ヘアリンス剤は毛髪に柔軟性、平滑性、帯電防止
性を付与し、かつ、毛髪のくし通シ性を良くして毛髪を
取り扱い易くする目的で使用され、普通第4級アンモニ
ウム塩をその主成分として配合している。しかし、これ
だけでは上記の諸効果に不十分な点が多いため、ヘアリ
ンス剤にはその性能を補うべく高級アルコール、グリセ
ライド、流動パラフィン、シリコン等の油脂類を配合す
るのが一般的である。
Conventionally, hair rinses have been used to impart flexibility, smoothness, and antistatic properties to hair, as well as to improve hair combability and make hair easier to handle. Contains it as the main ingredient. However, this alone is insufficient in many respects to achieve the above-mentioned effects, so it is common to add oils and fats such as higher alcohols, glycerides, liquid paraffin, and silicones to hair rinses to supplement their performance.

しかしながら、これら公知の成分の組合せでは、リンス
効果、すなわち毛髪に対する柔軟性、平滑性、帯電防止
性の付与効果が未だ完全でなく、特に乾燥状態における
リンス効果の低下という大きな問題があった。
However, with the combination of these known ingredients, the rinsing effect, that is, the effect of imparting flexibility, smoothness, and antistatic properties to hair, is still not perfect, and there is a major problem in that the rinsing effect is reduced, especially in dry conditions.

〔問題点を解決するための手段〕[Means for solving problems]

斯かる実状において、本発明者は上記問題点を解決すべ
く鋭意検討の結果、特定の分岐脂肪酸コレステリルエス
テルをリンス基剤として使用すれば乾燥状態でも優れた
リンス効果が発揮され、更に埼くべきことに毛髪に美し
い光沢を付与することができることを見出し、本発明を
完成した。
Under such circumstances, the present inventor has made extensive studies to solve the above problems, and has found that if a specific branched fatty acid cholesteryl ester is used as a rinse base, an excellent rinse effect can be exerted even in a dry state, and that it should be even stronger. In particular, they discovered that it is possible to impart beautiful luster to hair, and completed the present invention.

すなわち本発明は、次の二成分(A)及び(B)、(A
)第4級アンモニウム塩 0.1〜10重量%の)次の
式(I) c式中Rは合計11〜23個の炭素原子を有し、カルボ
キシル結合位から主鎖の中央までに、少くとも1つのア
ルキル置換基を有する飽和脂肪族炭化水素基である) で表わされる分岐脂肪酸コレステリルエステル0.1〜
10M量チ を含有するヘアリンス剤組成物を提供するものである。
That is, the present invention provides the following two components (A) and (B), (A
) quaternary ammonium salt 0.1 to 10% by weight) of the following formula (I) c, in which R has a total of 11 to 23 carbon atoms, and from the carboxyl bond position to the center of the main chain, there are a few Both are saturated aliphatic hydrocarbon groups having one alkyl substituent) Branched fatty acid cholesteryl ester represented by 0.1 to
A hair rinse composition containing a 10M amount of ti is provided.

本発明の(A)成分である第4級アンモニウム塩として
は、次の一般式(If) (式中、at −R4の1又は2個は炭素数8〜22の
直鎖もしくは分岐鎖の長鎖アルキル又は長鎖ヒドロキシ
アルキル基を残余は炭素数1〜3のアルキルもしくはヒ
ドロキシ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もしくは2のアルキル硫酸基を示す
) で−表わされる第4級アンモニウム塩の1種又は2種以
上の混合物が好ましく、これら(A)成分の代表的なも
のとしては、ステアリルトリメチルアンモニウムクロラ
イド、ジステアリルジメチルアンモニウムクロライド、
ステアリルトリメチルアンモニウムメトサルフェート、
N−ステアリル−N。
The quaternary ammonium salt which is the component (A) of the present invention has the following general formula (If) (wherein 1 or 2 of at -R4 is the length of a straight chain or branched chain having 8 to 22 carbon atoms). chain alkyl or long-chain hydroxyalkyl group, the remainder is an alkyl group having 1 to 3 carbon atoms, a hydroxyalkyl group, or a benzyl group, and X is a halogen atom or an alkyl sulfate group having 1 or 2 carbon atoms) One type or a mixture of two or more quaternary ammonium salts is preferred, and typical examples of these component (A) include stearyltrimethylammonium chloride, distearyldimethylammonium chloride,
stearyltrimethylammonium methosulfate,
N-stearyl-N.

N、N−トリ(ポリオキシエチレン)アンモニウムクロ
ライド(合計3モル付加)、セテルトリエテルアンモニ
ウムフ゛ロマイド、ステアリルベンジルジメチルアンモ
ニウムクロライド等が挙げられる。
Examples include N,N-tri(polyoxyethylene)ammonium chloride (addition of 3 moles in total), cetertrietherammonium chloride, stearylbenzyldimethylammonium chloride, and the like.

囚成分のヘアリンス剤組成物への配合量は、前記の如く
0.1〜10重量%(以下単に俤と略記する)、好まし
くは0.5〜3%である。
As mentioned above, the amount of the active ingredient added to the hair rinse composition is 0.1 to 10% by weight (hereinafter simply abbreviated as 迤), preferably 0.5 to 3%.

また、本発明の(B)成分である式(I)で表わされる
分岐脂肪酸コレステリルエステルは、分岐脂肪酸又はそ
の誘導体とコレステロールから通常のエヌテルを製造す
る方法Vこよって製造されるC%公昭59−23320
号公報)。分岐脂肪酸とコレステロールをそのまま反応
させてエステル化することもできるし、またいずれか−
力をより反応性の高い誘導体に導き、次いでエステル化
することもできる。
In addition, the branched fatty acid cholesteryl ester represented by formula (I), which is the component (B) of the present invention, is produced by the C% Kosho 59- 23320
Publication No.). Branched fatty acids and cholesterol can be directly reacted to form an ester, or either
It is also possible to direct the force to more reactive derivatives and then esterify them.

分岐脂肪酸コレステリルエステルの製造原料である分岐
脂肪酸(RCOOI()は炭素数12〜24(Rとして
の炭素数11〜23)のものが使用できるが、炭素数1
4〜20(Rとしての炭素数13〜19)のものが好ま
しく、特に炭素数18のものが最も好ましいものとして
挙げられる。分岐脂肪酸は、カルボキシル基結合位から
主鎖の中央までに少なくとも1つのアルキル置換基を有
する飽和分岐脂肪酸でらることが必要である。このよう
な飽和分岐脂肪酸は、石油化学工業原料又は油脂化学工
業原料よシ答易に得られる。
Branched fatty acids (RCOOI()), which is a raw material for producing branched fatty acid cholesteryl ester, can have 12 to 24 carbon atoms (R has 11 to 23 carbon atoms);
Those having 4 to 20 carbon atoms (R having 13 to 19 carbon atoms) are preferred, and those having 18 carbon atoms are most preferred. The branched fatty acid must be a saturated branched fatty acid having at least one alkyl substituent from the carboxyl group bonding position to the center of the main chain. Such saturated branched fatty acids can be easily obtained from petrochemical raw materials or oleochemical raw materials.

石油化学工業原料より得られるこのような分岐脂肪酸の
例としては、α位に側鎖を有する分岐脂肪酸があり、次
式(III)で表わされる。
An example of such a branched fatty acid obtained from petrochemical raw materials is a branched fatty acid having a side chain at the α position, and is represented by the following formula (III).

(式中RS及びR6はそれぞれ直鎖又は分岐鎖の飽和脂
肪族炭化水素基であり、R8及びR6の炭素原子数の和
は、12〜18である。) 上記の式(1)で表わされる0位に側鎖を有する分岐脂
肪酸は、例えば炭素数7〜10の直鎖又は分岐鎖のアル
デヒドのアルドール縮合によりα−分岐不飽和アルデヒ
ドとし、次いでこれを水素添加、酸化させて分岐飽和脂
肪酸とする方法によって製造することができる。
(In the formula, RS and R6 are each a linear or branched saturated aliphatic hydrocarbon group, and the sum of the number of carbon atoms of R8 and R6 is 12 to 18.) Represented by the above formula (1) A branched fatty acid having a side chain at the 0-position is, for example, converted into an α-branched unsaturated aldehyde by aldol condensation of a linear or branched aldehyde having 7 to 10 carbon atoms, and then hydrogenated and oxidized to form a branched saturated fatty acid. It can be manufactured by a method.

0位に側鎖を有する飽和分岐脂肪酸の好ましい具体例と
しては、5,7.7−トリメチル−2−(1,3,3−
トリメチルブチル)−オクタン酸、2−へブチルウンデ
カン酸、2−へキシルデカン酸等が例示される。
A preferred specific example of the saturated branched fatty acid having a side chain at position 0 is 5,7.7-trimethyl-2-(1,3,3-
Examples include trimethylbutyl)-octanoic acid, 2-hebutylundecanoic acid, and 2-hexyldecanoic acid.

油脂化学工業原料より得られる飽和分岐脂肪酸の例とし
ては、次の式(IV)で表わされるメチル分岐鎖を有す
る脂肪酸がおる。
An example of a saturated branched fatty acid obtained from oleochemical raw materials is a fatty acid having a methyl branched chain represented by the following formula (IV).

CHs (CHz )m−CH−(CHz )n−CO
OH(IV)CH3 1式中mとnの和は14であり、m = n = 7を
中心とする分布を有する) このようなメチル分岐鎖脂肪酸は、例えばルイン酸のダ
イマー製造時の副産物として得られ〔例えば、ジャーナ
ル・オブ・アメリカン・オイル・ケミスツ・ンサイエテ
イー(J、 Amer、 Off Chem。
CHs (CHz)m-CH-(CHz)n-CO
OH(IV)CH3 In formula 1, the sum of m and n is 14, and the distribution is centered around m = n = 7) Such methyl branched chain fatty acids are produced, for example, as a by-product during the production of luic acid dimers. [For example, Journal of American Oil Chemistry (J, Amer, Off Chem.

SOC,)51,522(1974))、本明細書中で
は、メチル分岐インステアリン酸と称する。メチル分岐
インステアリン酸は、例えばそのインプロピルエステル
として市販されている(米国エメリー社など)。
SOC, ) 51, 522 (1974)), herein referred to as methyl-branched instearic acid. Methyl-branched instearic acid is commercially available, for example as its inpropyl ester (eg Emery, USA).

また、コレステロールは種々の方法で製造したもののほ
か、天然物質から抽出または抽出精製により得られたも
の、例えば乾燥した牛の脳、を髄等から得たものも使用
できる。
In addition to cholesterol produced by various methods, it is also possible to use cholesterol extracted from natural substances or obtained by extraction and purification, such as the pulp of dried cow brain.

これらの分岐脂肪酸コレステリルエステルの内でもメチ
ル分岐インステアリン酸コレステリルエステルが最も好
ましい。
Among these branched fatty acid cholesteryl esters, methyl branched instearic acid cholesteryl ester is most preferred.

分岐脂肪酸コレステリルエステル(1)は、本発明のヘ
アリンス剤組成物中に0.1〜10. O%、特に好ま
しくは0.2〜2チとなるように配合される。
The branched fatty acid cholesteryl ester (1) is contained in the hair rinse composition of the present invention in an amount of 0.1 to 10. 0%, particularly preferably 0.2 to 2%.

0.1%より少ないと本発明効果が十分奏されず、10
.0%を越えると系がゲル化するため好ましくない。
If it is less than 0.1%, the effects of the present invention will not be sufficiently exhibited;
.. If it exceeds 0%, the system will gel, which is not preferable.

本発明組成物は、前記囚及びω)成分を、水、エタノー
ル、クリセリン、エチレングリコール、フロピレンゲリ
コール、1.3−プロパンジオール、インプロパツール
、ポリエチレングリコール等の適当な溶剤に溶解ないし
は分散させることにより調製される。
In the composition of the present invention, the above-mentioned components and ω) are dissolved or dispersed in a suitable solvent such as water, ethanol, chrycerin, ethylene glycol, propylene gellicol, 1,3-propanediol, inpropatol, polyethylene glycol, etc. It is prepared by

本発明組成物には、更にその目的及び必要に応じて通常
ヘアリンス剤組成物に用いられる公知成分を配合するこ
とができ、その中でも(A)成分以外のカチオン性界面
活性剤、乳化補助剤としてのアニオン性界面活性剤、非
イオン性界面活性剤及び両性界面活性剤から選ばれる界
面活性剤を配合するのが好ましい。これらの界面活性剤
はへブーリンス等組成中にo、oi〜10%、好ましく
は0.5〜5%配合するのがよい結果を与える。
The composition of the present invention may further contain known ingredients commonly used in hair rinse compositions, depending on the purpose and necessity, including cationic surfactants other than component (A) and emulsification aids. It is preferable to blend a surfactant selected from anionic surfactants, nonionic surfactants, and amphoteric surfactants. Good results can be obtained by blending these surfactants in the composition of Hebo Rinse etc. in an amount of O, Oi to 10%, preferably 0.5 to 5%.

更に、本発明組成物には、任意成分として流動パラフィ
ン、ワセリン、固型パラフィン等の炭化水素;液状ラノ
リン、ラノリン脂肪酸等のラノリン誘導体;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、グリコ
ール変性ポリシロキサン等のシリコン誘導体;ポリオキ
シプロピレン−ポリオキシエチレン共重合体並びにその
エーテル化物、エステル、高級アルコール等の油剤、殺
菌剤、紫外線吸収剤、香料、色素等が挙げられる1、〔
発明の効果〕 本発明のヘアリンス剤組成物は、従来品と異なって、麦
が乾燥状態のときでも良好なリンス効果を発揮すること
ができる。
Furthermore, the composition of the present invention may optionally contain hydrocarbons such as liquid paraffin, vaseline, and solid paraffin; lanolin derivatives such as liquid lanolin and lanolin fatty acids; dimethylpolysiloxane, methylphenylpolysiloxane, and glycol-modified polysiloxane. Silicon derivatives; examples include polyoxypropylene-polyoxyethylene copolymers and their ethers, esters, oils such as higher alcohols, disinfectants, ultraviolet absorbers, fragrances, pigments, etc. 1.
Effects of the Invention The hair rinse agent composition of the present invention, unlike conventional products, can exhibit a good rinsing effect even when the wheat is in a dry state.

〔実施例〕〔Example〕

次に実施例を挙げて説明する。 Next, an example will be given and explained.

実施例1 第1表に示すヘアリンス剤組成物を常法に従って調製し
、その性能を下記方法により評価した。
Example 1 The hair rinse composition shown in Table 1 was prepared according to a conventional method, and its performance was evaluated by the following method.

(+)<L通り力 302の入毛を40℃の水で湿らせ、202の水を含ま
せる。次いで、ヘアリンス剤組成物12を均一に塗布、
すすぎ操作を2回繰返し、しぼった状態でストレインゲ
ージに設置し、クシでとき、その時にかかる力を測定す
る(湿時)。
(+)<L Hair with a passing force of 302 is moistened with water at 40° C. to contain water of 202. Next, uniformly apply the hair rinse composition 12,
Repeat the rinsing operation twice, place it on a strain gauge in the squeezed state, comb it with a comb, and measure the force applied at that time (when wet).

更に、ドライヤーで乾燥し、20℃、65チRHの恒温
恒湿室に一夜放置後、ストレインゲージに設置し、クシ
でとき、その時にかかる力を測定する(乾燥時)。
Further, it was dried with a hair dryer, left overnight in a constant temperature and humidity room at 20° C. and 65° RH, placed on a strain gauge, and then combed with a comb to measure the force applied at that time (during drying).

(11)  ヘアフライ 上記(1)の「クシ通し」の乾燥時の測定の際に静電気
によるヘアフライ現象が発生するか否かを観察する。
(11) Hair frying It is observed whether or not a hair frying phenomenon occurs due to static electricity during the drying measurement of "combing through" in (1) above.

評価基準: ○ ヘアフライが起こる × ヘアフライが起こらない (i)  光沢賦与効果 日本人女性の黒色毛109を夫々のヘアリンス剤組成物
で処理(A0”C130分)シ、乾燥後の光沢を無処理
毛(対照)と比較し、以下の基準で光沢賦与効果を評価
した。
Evaluation criteria: ○ Hair fly occurs × Hair fly does not occur (i) Shine-imparting effect Japanese women's black hair 109 was treated with each hair rinse composition (A0''C130 minutes), and the shine after drying was compared to untreated hair. (Control), and the gloss imparting effect was evaluated using the following criteria.

×:対照と差を認めない △:わずかな光沢賦与効果を誌める ○:明らかな光沢賦与効果を認める ◎:顕著な光沢賦与効果を認める 以下余白×: No difference from control △: Slight gloss imparting effect ○: Obvious gloss imparting effect recognized ◎: Remarkable gloss imparting effect recognized Margin below

Claims (1)

【特許請求の範囲】 1、次の二成分(A)及び(B)、 (A)第4級アンモニウム塩0.1〜10重量%(B)
次の式( I ) ▲数式、化学式、表等があります▼( I ) (式中Rは合計11〜23個の炭素原子を有し、カルボ
キシル結合位から主鎖の中央までに、少くとも1つのア
ルキル置換基を有する飽和脂肪族炭化水素基である) で表わされる分岐脂肪酸コレステリルエステル0.1〜
10重量% を含有するヘアリンス剤組成物。 2、(A)成分が次の一般式(II) ▲数式、化学式、表等があります▼(II) (式中、R_1〜R_4の1又は2個は炭素数8〜22
の直鎖もしくは分岐鎖の長鎖アルキル又は長鎖ヒドロキ
シアルキル基を、残余は炭素数1〜3のアルキルもしく
はヒドロキシ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もしくは2のアルキル硫酸基を
示す) で表わされる第4級アンモニウム塩の1種又は2種以上
の混合物である特許請求の範囲第1項記載のヘアリンス
剤組成物。
[Claims] 1. The following two components (A) and (B): (A) 0.1 to 10% by weight of quaternary ammonium salt (B)
The following formula (I) ▲Mathematical formulas, chemical formulas, tables, etc.▼(I) (In the formula, R has a total of 11 to 23 carbon atoms, and at least 1 A branched fatty acid cholesteryl ester represented by (a saturated aliphatic hydrocarbon group having two alkyl substituents) 0.1 to
A hair rinse composition containing 10% by weight. 2. (A) component is the following general formula (II) ▲ There are mathematical formulas, chemical formulas, tables, etc. ▼ (II) (In the formula, 1 or 2 of R_1 to R_4 has a carbon number of 8 to 22
The remainder is an alkyl or hydroxyalkyl group having 1 to 3 carbon atoms or a benzyl group, and X is a halogen atom or an alkyl sulfate having 1 or 2 carbon atoms. The hair rinse composition according to claim 1, which is one or a mixture of two or more quaternary ammonium salts represented by the following formula.
JP21196985A 1985-09-25 1985-09-25 Hair rinse agent composition Granted JPS6272607A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP21196985A JPS6272607A (en) 1985-09-25 1985-09-25 Hair rinse agent composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP21196985A JPS6272607A (en) 1985-09-25 1985-09-25 Hair rinse agent composition

Publications (2)

Publication Number Publication Date
JPS6272607A true JPS6272607A (en) 1987-04-03
JPH0236566B2 JPH0236566B2 (en) 1990-08-17

Family

ID=16614706

Family Applications (1)

Application Number Title Priority Date Filing Date
JP21196985A Granted JPS6272607A (en) 1985-09-25 1985-09-25 Hair rinse agent composition

Country Status (1)

Country Link
JP (1) JPS6272607A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5466442A (en) * 1991-07-19 1995-11-14 Kao Corporation Cholesteryl silicone derivative and cosmetic composition comprising the same
DE102009043466A1 (en) * 2009-09-30 2011-03-31 Beiersdorf Ag Active agent combination, useful e.g. to prepare hair cosmetic preparation and for care or repair of damaged hairs, comprises oryzanol and cholesteryl compounds with liquid crystalline properties under normal conditions

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0319789U (en) * 1989-07-07 1991-02-26
JPH0675976U (en) * 1993-04-09 1994-10-25 株式会社ニチワ Bicycle parking equipment

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS56167611A (en) * 1980-05-29 1981-12-23 Nisshin Oil Mills Ltd:The Cosmetic and external use preparation

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS56167611A (en) * 1980-05-29 1981-12-23 Nisshin Oil Mills Ltd:The Cosmetic and external use preparation

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5466442A (en) * 1991-07-19 1995-11-14 Kao Corporation Cholesteryl silicone derivative and cosmetic composition comprising the same
DE102009043466A1 (en) * 2009-09-30 2011-03-31 Beiersdorf Ag Active agent combination, useful e.g. to prepare hair cosmetic preparation and for care or repair of damaged hairs, comprises oryzanol and cholesteryl compounds with liquid crystalline properties under normal conditions

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