JP6012394B2 - Hair elasticity improver and hair cosmetic - Google Patents

Hair elasticity improver and hair cosmetic Download PDF

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JP6012394B2
JP6012394B2 JP2012234080A JP2012234080A JP6012394B2 JP 6012394 B2 JP6012394 B2 JP 6012394B2 JP 2012234080 A JP2012234080 A JP 2012234080A JP 2012234080 A JP2012234080 A JP 2012234080A JP 6012394 B2 JP6012394 B2 JP 6012394B2
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徳雄 中根
徳雄 中根
卓司 野澤
卓司 野澤
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Toho Chemical Industry Co Ltd
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本発明は、毛髪弾力性向上剤に関し、さらに詳しくは日常での物理的、化学的作用により損傷を受けた毛髪の弾力性を改善するための毛髪弾力性向上剤、並びに毛髪弾力性向上剤を含有し毛髪の弾力性を改善する効果を有し、毛髪に良好な使用性(ハリ・コシ感、滑らかさ、ベタツキ感の無さ)を付与する毛髪化粧料に関する。   The present invention relates to a hair elasticity improver, and more particularly a hair elasticity improver for improving the elasticity of hair damaged by daily physical and chemical action, and a hair elasticity improver. The present invention relates to a hair cosmetic composition that has an effect of improving the elasticity of hair and imparts good usability (harshness, firmness, smoothness, no stickiness) to hair.

近年、ヘアスタイルの多様化に伴って、毛髪はヘアカラー剤、ブリーチ剤、パーマネントウェーブ剤、縮毛矯正剤等で処理される機会が増えている。これらの薬剤等による化学的作用及び日常的なドライヤー熱やブラッシング等のヘアケア行動による物理的作用が毛髪の損傷を促進し、毛髪本来の弾力性、ハリ・コシ感、滑らかさを失わせる要因となっている。そこでこのような損傷毛髪の改善に水分を補給する方法や、油分をコーティングする方法が用いられてきたが一時的な効果に過ぎず、根本的な改善には至らなかった。   In recent years, with the diversification of hairstyles, the opportunity for hair to be treated with hair coloring agents, bleaching agents, permanent wave agents, hair straighteners and the like has increased. The chemical action of these chemicals and the physical action of hair care behavior such as daily dryer heat and brushing promote hair damage and cause the loss of elasticity, elasticity, firmness and smoothness of the hair. It has become. Therefore, a method of supplying water and a method of coating oil have been used to improve such damaged hair, but this was only a temporary effect and did not lead to a fundamental improvement.

そこで、特許文献1には塩基性アミノ酸であるアルギニンを有効成分とし、この有効成分が毛髪の芯まで届くことにより傷んだ毛髪を治し、毛髪本来の美しさと健康を取り戻す毛髪健全化剤が提案され、また特許文献2には酸性アミノ酸と塩基性アミノ酸の2種のアミノ酸を併用することで毛髪内部から作用して毛髪補修とスタイリングを同時に行うことができる毛髪化粧料等が提案されているが、アミノ酸の利用だけでは毛髪の弾力性向上効果は不十分であった。   Therefore, Patent Document 1 proposes a hair-healing agent that uses arginine, which is a basic amino acid, as an active ingredient, cures damaged hair when it reaches the core of the hair, and restores the original beauty and health of the hair. In addition, Patent Document 2 proposes a hair cosmetic or the like that can act from the inside of the hair and simultaneously perform hair repair and styling by using two types of amino acids, acidic amino acid and basic amino acid. The effect of improving the elasticity of the hair was insufficient only by using amino acids.

一方、特許文献3には、副生塩を含まない化粧料等に好適なタウリン誘導体の製造方法が開示されているが、炭素数12以上の長鎖アルキル基を有する界面活性を期待するものであり、毛髪弾力性向上剤とは本質的に異なるものであった。   On the other hand, Patent Document 3 discloses a method for producing a taurine derivative suitable for cosmetics and the like that do not contain by-product salts, but is expected to have a surface activity having a long-chain alkyl group having 12 or more carbon atoms. Yes, it was essentially different from the hair elasticity improver.

特開2001−81013号公報(1−14頁)JP 2001-81013 A (page 1-14) 特開2004−346040号公報(1−14頁)JP 2004-346040 A (page 1-14) 特開平10−218854号公報 (1−5頁)JP-A-10-218854 (page 1-5)

本発明は、毛髪弾力性向上剤に関し、さらに詳しくは日常での物理的、化学的作用により損傷を受けた毛髪の弾力性を改善するための毛髪弾力性向上剤、並びに毛髪弾力性向上剤を含有し毛髪の弾力性を改善する効果を有し、毛髪に良好な使用性(ハリ・コシ感、滑らかさ、ベタツキ感の無さ)を付与する毛髪化粧料を提供することにある。   The present invention relates to a hair elasticity improver, and more particularly a hair elasticity improver for improving the elasticity of hair damaged by daily physical and chemical action, and a hair elasticity improver. It is an object of the present invention to provide a hair cosmetic that contains an effect of improving the elasticity of hair and imparts good usability (harshness, firmness, smoothness, no stickiness) to hair.

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、
下記一般式(1)

Figure 0006012394
(式中、R、Rのいずれか一方/又は両方は、下記一般式(2)で表される基、残りは水素原子を表し、Mは水素原子、アルカリ金属、アルカリ土類金属、アンモニウム及び有機アミン類から選ばれる少なくとも1種を表す。)
Figure 0006012394
(式中、Rは直鎖又は分岐した炭素数1〜8のアルキル基、アルケニル基もしくはヒドロキシアルキル基)
で表されるタウリン誘導体からなる毛髪弾力性向上剤が優れた毛髪弾力性改善効果を有することを見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
The following general formula (1)
Figure 0006012394
(In the formula, either one or both of R 1 and R 2 are groups represented by the following general formula (2), the rest represent a hydrogen atom, M is a hydrogen atom, an alkali metal, an alkaline earth metal, Represents at least one selected from ammonium and organic amines.)
Figure 0006012394
(Wherein R 3 is a linear or branched alkyl group having 1 to 8 carbon atoms, an alkenyl group or a hydroxyalkyl group)
The present inventors have found that a hair elasticity improving agent comprising a taurine derivative represented by the above has an excellent effect of improving hair elasticity.

すなわち、本発明は上記一般式(1)で示されるタウリン誘導体からなる毛髪弾力性向上剤、並びに該毛髪弾力性向上剤を含有してなる毛髪化粧料が毛髪の弾力性を改善する効果を有し、毛髪に良好な使用性(ハリ・コシ感、滑らかさ、ベタツキ感の無さ)を付与することができる。   That is, the present invention has the effect that the hair elasticity improver comprising the taurine derivative represented by the general formula (1) and the hair cosmetic containing the hair elasticity improver improve the elasticity of the hair. In addition, the hair can be given good usability (harshness, firmness, smoothness, no stickiness).

以下に、本発明の毛髪弾力性向上剤、並びに該毛髪弾力性向上剤を含有する毛髪化粧料について詳述する。
本発明の毛髪弾力性向上剤であるタウリン誘導体の製造方法としては特に限定はないが、一般的に下式で示される方法で製造可能である。

Figure 0006012394
(式中、R、Mは前記と同じ。) Below, the hair elasticity improving agent of this invention and the hair cosmetics containing this hair elasticity improving agent are explained in full detail.
Although there is no limitation in particular as a manufacturing method of the taurine derivative which is a hair elasticity improvement agent of this invention, it can manufacture with the method generally shown by the following Formula.
Figure 0006012394
(Wherein R 3 and M are the same as described above.)

上記で表されるタウリン誘導体の具体的製造方法としては、タウリン誘導体の有効成分が10〜90%となるように、水系及び/又は溶媒系或いは水溶媒混合系溶媒中(混合系溶媒の場合は水:溶媒=5:95〜95:5)、タウリン1モルをアルカリで中和してタウリン塩溶液を得て、同温〜95℃で0.8〜2.2モルのグリシジルエーテルを一括或いは滴下するなどの方法で添加し、60〜95℃で反応が終了するまで熟成する。ここでグリシジルエーテルはタウリン1モル対して0.9〜〜2モル、熟成温度70〜90℃、熟成時間1から10時間がより好ましい。   As a specific method for producing the taurine derivative represented above, the active ingredient of the taurine derivative is 10 to 90% in an aqueous system and / or a solvent system or an aqueous solvent mixed system solvent (in the case of a mixed system solvent). Water: solvent = 5: 95 to 95: 5), 1 mol of taurine is neutralized with an alkali to obtain a taurine salt solution, and 0.8 to 2.2 mol of glycidyl ether is collectively or at the same temperature to 95 ° C. It is added by a method such as dropping, and ripened at 60 to 95 ° C. until the reaction is completed. The glycidyl ether is more preferably 0.9 to 2 mol, an aging temperature of 70 to 90 ° C., and an aging time of 1 to 10 hours with respect to 1 mol of taurine.

タウリン誘導体の中和に用いるアルカリとしては、リチウム、カリウム、ナトリウム等のアルカリ金属、カルシウム、マグネシウム等のアルカリ土類金属の他、水酸化リチウム、水酸化カリウム、水酸化ナトリウム等のアルカリ金属水酸化物、水酸化カルシウム、水酸化マグネシウム等のアルカリ土類金属水酸化物が好ましく用いることができる。また、アンモニアやモノエタノールアミン、ジエタノールアミン、トリエタノールアミン等の有機アミン類も好ましく用いることができる。   Examples of the alkali used for neutralizing the taurine derivative include alkali metals such as lithium, potassium and sodium, alkaline earth metals such as calcium and magnesium, and alkali metal hydroxides such as lithium hydroxide, potassium hydroxide and sodium hydroxide. And alkaline earth metal hydroxides such as calcium hydroxide and magnesium hydroxide can be preferably used. In addition, organic amines such as ammonia, monoethanolamine, diethanolamine, and triethanolamine can be preferably used.

タウリン誘導体の製造に用いるグリシジルエーテルとしては、炭素数1〜8、好ましくは炭素数1〜4のアルキル基、アルケニル基、ヒドロキシアルキル基を有するグリシジルエーテル、具体的には、メチルグリシジルエーテル、エチルグリシジルエーテル、n−プロピルグリシジルエーテル、i−プロピルグリシジルエーテル、n−ブチルグリシジルエーテル、i−ブチルグリシジルエーテル、n−ペンチルグリシジルエーテル、2−エチルヘキシル−グリシジルエーテル、ビニルグリシジルエーテル、アリルグリシジルエーテル、2−メチルアリルグリシジルエーテル、ブテニルグリシジルエーテル、オクテニルグリシジルエーテル、2−エチルヘキセニルグリシジルエーテル等が挙げられ、四日市合成(株)製「エポゴーセー」シリーズ、日油(株)製「エピオール」シリーズ等として市販されているが、特にこれらに限定されるものではない。   The glycidyl ether used for the production of the taurine derivative is a glycidyl ether having an alkyl group, alkenyl group or hydroxyalkyl group having 1 to 8 carbon atoms, preferably 1 to 4 carbon atoms, specifically methyl glycidyl ether or ethyl glycidyl. Ether, n-propyl glycidyl ether, i-propyl glycidyl ether, n-butyl glycidyl ether, i-butyl glycidyl ether, n-pentyl glycidyl ether, 2-ethylhexyl-glycidyl ether, vinyl glycidyl ether, allyl glycidyl ether, 2-methyl Allyl glycidyl ether, butenyl glycidyl ether, octenyl glycidyl ether, 2-ethylhexenyl glycidyl ether and the like are listed. “Epogosei” series manufactured by Yokkaichi Synthesis Co., Ltd. , Are commercially available as NOF Co., Ltd. "EPIOL" series, etc., but the present invention is not particularly limited to these.

また、タウリン誘導体は水系のみでの製造も可能であるが、エタノール、2−プロパノール等の低級アルコール類、プロピレングリコール、ジプロピレングリコール,1,3−ブチレングリコール等の多価アルコール類、アセトン等のケトン類などの溶媒或いは水溶媒混合溶媒中での製造も可能であり、これらの中でもエタノール、2−プロパノールが特に好適に用いられる。反応系中のタウリン誘導体の有効成分は30〜60%、水系及び/又は溶媒系或いは水溶媒混合系溶媒中(混合溶媒の場合は水:溶媒=20:80〜90:10)、特に水系での製造がより好ましい。   Taurine derivatives can be produced only in an aqueous system, but lower alcohols such as ethanol and 2-propanol, polyhydric alcohols such as propylene glycol, dipropylene glycol and 1,3-butylene glycol, acetone and the like. Production in a solvent such as ketones or an aqueous solvent mixed solvent is also possible, and among these, ethanol and 2-propanol are particularly preferably used. The active ingredient of the taurine derivative in the reaction system is 30 to 60%, in an aqueous system and / or a solvent system or an aqueous solvent mixed solvent (in the case of a mixed solvent, water: solvent = 20: 80 to 90:10), particularly in an aqueous system. Is more preferable.

得られたタウリン誘導体はそのまま本発明品に用いることもできるが、イオン交換樹脂、シリカゲル等を用いたカラム精製など通常の精製方法により精製し用いることもできる。本発明のタウリン誘導体は他の方法でも製造でき、製造方法としては特に限定はない。   The obtained taurine derivative can be used as it is for the product of the present invention, but can also be purified and used by a conventional purification method such as column purification using an ion exchange resin, silica gel or the like. The taurine derivative of the present invention can be produced by other methods, and the production method is not particularly limited.

本発明の毛髪弾力性向上剤の毛髪化粧料への配合量は、0.01〜20重量%、特には0.05〜10重量%が好ましい。0.01%未満の配合では毛髪弾力性改善効果が不十分であり、20%以上配合しても使用性にべたつきを感じるようになり好ましくない。   The blending amount of the hair elasticity improving agent of the present invention into the hair cosmetic is preferably 0.01 to 20% by weight, particularly preferably 0.05 to 10% by weight. If the blending is less than 0.01%, the effect of improving hair elasticity is insufficient, and even if blending more than 20%, the usability becomes sticky, which is not preferable.

本発明の毛髪弾力性向上剤を含有してなる毛髪化粧料は、毛髪に使用する任意の組成物に適用可能であり、透明液状、ジェル状、クリーム状、乳液上、ムース状等の剤形から適宜選択することができ、シャンプー等の毛髪洗浄剤、ヘアリンス、ヘアコンディショナー、ヘアトリートメント、ヘアパック、ヘアスプレー、スタイリング剤、ヘアカラー剤、ブリーチ剤、パーマネントウェーブ剤、縮毛矯正剤等の毛髪処理剤等が挙げられ、使用形態も毛髪に塗布し全体になじませた後すすぎ流すものや、洗い流さないもの等いずれも好適に用いられる。   The hair cosmetic composition containing the hair elasticity improving agent of the present invention is applicable to any composition used for hair, and is in the form of a transparent liquid, gel, cream, on milk, mousse, etc. Hair such as shampoos, hair rinses, hair conditioners, hair treatments, hair packs, hair sprays, styling agents, hair color agents, bleach agents, permanent wave agents, hair straighteners, etc. A treatment agent and the like can be mentioned, and any of the usage forms such as those which are applied to the hair and applied to the hair and then rinsed and those which are not washed off are suitably used.

本発明の毛髪弾力性向上剤を含有してなる毛髪化粧料には、毛髪弾力性向上剤以外に必要に応じカチオン界面活性剤、油性成分、カチオン性ポリマー等を配合することができる。   In the hair cosmetic composition containing the hair elasticity improver of the present invention, in addition to the hair elasticity improver, a cationic surfactant, an oil component, a cationic polymer and the like can be blended as necessary.

カチオン界面活性剤としては、4級アンモニウム塩及び/又は3級アミンを用いることができ、4級アンモニウム塩として、アルキルトリメチルアンモニウム塩、アルキルアミドアミン、アルキルヒドロキシエーテルアミンなどが挙げられ、具体的に、ラウリルトリモニウムクロリド、ミリスチルトリモニウムクロリド、セチルトリモニウムクロリド、ステアリルトリモニウムクロリド、ベヘントリモニウムクロリド、ラウリルトリモニウムブロミド、ミリスチルトリモニウムブロミド、セチルトリモニウムブロミド、ステアリルトリモニウムブロミド、ベヘニルトリモニウムブロミド、ラウリルPGトリモニウムクロリド、ミリスチルPGトリモニウムクロリド、セチルPGトリモニウムクロリド、ステアリルPGトリモニウムクロリド、ベヘニルPGトリモニウムクロリド、ラウリルPGトリモニウムブロミド、ミリスチルPGトリモニウムブロミド、セチルPGトリモニウムブロミド、ステアリルPGトリモニウムブロミド、ベヘニルPGトリモニウムブロミド、ジセチルジモニウムクロリド、ジステアリルジモニウムクロリド、ジココジモニウムクロリドなど;3級アミンとして、ラウリルジメチルアミン、ミリスチルジメチルアミン、セチルジメチルアミン、ステアリルジメチルアミン、オレイルジメチルアミン、イソステアリルジメチルアミン、アラキルジメチルアミン、ベヘニルジメチルアミン、ラウラミドプロピルジメチルアミン、ミリスタミドプロピルジメチルアミン、パルミタミドプロピルジメチルアミン、ステアラミドプロピルジメチルアミン、オレアミドプロピルジメチルアミン、イソステアラミドプロピルジメチルアミン、アラキナミドプロピルジメチルアミン、ベヘナミドプロピルジメチルアミン、ステアラミドエチルジエチルアミン、アラキナミドエチルジエチルアミン、ベヘナミドエチルジエチルアミン、ラウリルPGジメチルアミン、ミリスチルPGジメチルアミン、セチルPGジメチルアミン、ステアリルPGジメチルアミン、ベヘニルPGジメチルアミン等が挙げられ、これらの中でもステアリルトリモニウムクロリド、ベヘントリモニウムクロリドが特に好適に用いられる。   As the cationic surfactant, a quaternary ammonium salt and / or a tertiary amine can be used, and examples of the quaternary ammonium salt include alkyltrimethylammonium salt, alkylamidoamine, alkylhydroxyetheramine, and the like. Lauryltrimonium chloride, myristyltrimonium chloride, cetyltrimonium chloride, stearyltrimonium chloride, behentrimonium chloride, lauryltrimonium bromide, myristyltrimonium bromide, cetyltrimonium bromide, stearyltrimonium bromide, behenyltrimonium bromide, Lauryl PG trimonium chloride, myristyl PG trimonium chloride, cetyl PG trimonium chloride, stearyl PG trimonium chloride, Henyl PG trimonium chloride, lauryl PG trimonium bromide, myristyl PG trimonium bromide, cetyl PG trimonium bromide, stearyl PG trimonium bromide, behenyl PG trimonium bromide, dicetyl dimonium chloride, distearyl dimonium chloride, dicocodimomo Nitric chloride, etc .; tertiary amines such as lauryl dimethylamine, myristyl dimethylamine, cetyl dimethylamine, stearyl dimethylamine, oleyl dimethylamine, isostearyl dimethylamine, aralkyl dimethylamine, behenyl dimethylamine, lauramidopropyl dimethylamine, myrista Midpropyldimethylamine, palmitamidopropyldimethylamine, stearamidepropyldimethylamine, oleamide Lopyldimethylamine, isostearamidpropyldimethylamine, araquinamidepropyldimethylamine, behenamidopropyldimethylamine, stearamideethyldiethylamine, araquinamidoethyldiethylamine, behenamidoethyldiethylamine, laurylPGdimethylamine, myristyl PG Examples include dimethylamine, cetyl PG dimethylamine, stearyl PG dimethylamine, and behenyl PG dimethylamine. Among these, stearyl trimonium chloride and behentrimonium chloride are particularly preferably used.

また3級アミンは無機酸及び/又は有機酸で中和され塩として用いられるが、無機酸及び/又は有機酸の具体例としては、塩酸、硫酸、リン酸、酢酸、乳酸、グリコール酸、クエン酸、グルタミン酸、リンゴ酸、コハク酸等が挙げられ、これらの中から1種又は2種を任意に用いることができる。   Tertiary amines are neutralized with inorganic acids and / or organic acids and used as salts. Specific examples of inorganic acids and / or organic acids include hydrochloric acid, sulfuric acid, phosphoric acid, acetic acid, lactic acid, glycolic acid, citric acid. An acid, glutamic acid, malic acid, succinic acid, etc. are mentioned, Among these, 1 type or 2 types can be used arbitrarily.

本発明では、これらのカチオン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、毛髪化粧料中の配合量は、0.1〜20重量%が好ましい。   In the present invention, one or more of these cationic surfactants can be arbitrarily used, and the blending amount in the hair cosmetic is preferably 0.1 to 20% by weight.

油性成分としては、室温で液体或いは固体のいずれも含み、高級アルコール、高級脂肪酸、エステル油類、シリコーン、炭化水素類等が挙げられ、これらから好適なものを適宜選択すればよい。   Examples of the oil component include liquids and solids at room temperature, and include higher alcohols, higher fatty acids, ester oils, silicones, hydrocarbons, and the like, and suitable ones may be appropriately selected from these.

油性成分の具体例としては、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などの高級アルコール;ミリスチン酸、パルミチン酸、ステアリン酸、ベヘン酸、オレイン酸、イソステアリン酸、イソパルミチン酸などの高級脂肪酸;ミリスチン酸イソプロピル、パルミチン酸イソプロピル、オクタン酸セチル、オレイン酸オレイル、ミリスチン酸オクチルドデシル、ラウリン酸ヘキシル、乳酸セチル、モノステアリン酸プロピレングリコール、オレイン酸オレイル、2−エチルヘキサン酸ヘキサデシル、イソノナン酸イソノニル、イソノナン酸トリデシル等のエステル油、ヒマシ油、カカオ油、ミンク油、アボガド油、オリーブ油等のグリセリド、ミツロウ、鯨ロウ、ラノリン、カルナウバロウ等のロウ類などのエステル油類;ジメチコン、ジメチコノール、メチルフェニルポリシロキサン、ジフェニルポリシロキサン等の鎖状ポリシロキサン、デカメチルシクロペンタシロキサン、ドデカメチルシクロペンタシロキサン等の環状ポリシロキサン、3次元網目構造を有するシリコーン樹脂、シリコーンゴム、アミノ変性シリコーン、脂肪酸変性ポリシロキサン、アルコール変性シリコーン、脂肪族変性ポリシロキサン、ポリエーテル変性シリコーン、エポキシ変性シリコーン、フッ素変性シリコーン、アルキル変性シリコーンなどのシリコーン;流動パラフィン、スクワラン、スクワレン、パラフィン、イソパラフィン、ワセリンなどの炭化水素が挙げられるが、特に限定されるものではない。   Specific examples of the oil component include higher alcohols such as myristyl alcohol, cetyl alcohol, stearyl alcohol, cetostearyl alcohol, behenyl alcohol, batyl alcohol, and isostearyl alcohol; myristic acid, palmitic acid, stearic acid, behenic acid, oleic acid, isostearic acid Acids, higher fatty acids such as isopalmitic acid; isopropyl myristate, isopropyl palmitate, cetyl octanoate, oleyl oleate, octyldodecyl myristate, hexyl laurate, cetyl lactate, propylene glycol monostearate, oleyl oleate, 2- Ester oil such as hexadecyl ethylhexanoate, isononyl isononanoate, tridecyl isononanoate, castor oil, cacao oil, mink oil, avocado oil, olive oil Ester oils such as glycerides such as buoy oil, waxes such as beeswax, spermaceti, lanolin and carnauba wax; chain polysiloxanes such as dimethicone, dimethiconol, methylphenylpolysiloxane, diphenylpolysiloxane, decamethylcyclopentasiloxane, dodeca Cyclic polysiloxanes such as methylcyclopentasiloxane, silicone resins having a three-dimensional network structure, silicone rubber, amino-modified silicone, fatty acid-modified polysiloxane, alcohol-modified silicone, aliphatic-modified polysiloxane, polyether-modified silicone, epoxy-modified silicone, Silicone such as fluorine-modified silicone and alkyl-modified silicone; and hydrocarbons such as liquid paraffin, squalane, squalene, paraffin, isoparaffin, petrolatum, etc. The present invention is not limited to.

本発明では、これらの油性成分の中から1種又は2種以上を任意に用いることができ、毛髪化粧料中の配合量は、0.01〜20重量%が好ましい。   In this invention, 1 type (s) or 2 or more types can be arbitrarily used from these oil-based components, and the compounding quantity in hair cosmetics has preferable 0.01-20 weight%.

カチオン性ポリマーとしては、カチオン化セルロース、カチオン化グアーガム、カチオン化デンプン、カチオン化デキストラン、カチオン化ガラクトマンナン、ジアリル4級アンモニウム塩のホモポリマー、ジアリル4級アンモニウム塩/アクリルアミド共重合体、4級化ポリビニルピロリドン誘導体、ポリグリコールポリアミン縮合物、ビニルイミダゾリニウムトリクロライド/ビニルピロリドン共重合体、ヒドロキシエチルセルロース/ジメチルジアリルアンモニウムクロライド共重合体、ビニルピロリドン/4級化ジメチルアミノエチルメタクリレート共重合体、ポリビニルピロリドン/アルキルアミノアクリレート/ビニルカプロラクタム共重合体、ビニルピロリドン/メタクリルアミドプロピル塩化トリメチルアンモニウム共重合体、アルキルアクリルアミド/アクリレート/アルキルアミノアルキルアクリルアミド/ポリエチレングリコールメタクリレート共重合体、アジピン酸/ジメチルアミノヒドロキシプロピルジエチレントリアミン共重合体等が挙げられるが、特に限定されるものではない。   Cationic polymers include cationized cellulose, cationized guar gum, cationized starch, cationized dextran, cationized galactomannan, homopolymer of diallyl quaternary ammonium salt, diallyl quaternary ammonium salt / acrylamide copolymer, quaternization. Polyvinyl pyrrolidone derivatives, polyglycol polyamine condensate, vinyl imidazolinium trichloride / vinyl pyrrolidone copolymer, hydroxyethyl cellulose / dimethyl diallylammonium chloride copolymer, vinyl pyrrolidone / quaternized dimethylaminoethyl methacrylate copolymer, polyvinyl pyrrolidone / Alkylaminoacrylate / vinylcaprolactam copolymer, vinylpyrrolidone / methacrylamidopropyl trimethylammonium chloride copolymer , Alkyl acrylamide / acrylate / alkylaminoalkyl acrylamide / polyethylene glycol methacrylate copolymers, although adipic acid / dimethyl amino hydroxypropyl diethylene triamine copolymers, and the like, but is not particularly limited.

本発明では、これらのカチオン性ポリマーの中から1種又は2種以上を任意に用いることができ、毛髪化粧料中の配合量は、0.1〜10重量%が好ましい。   In this invention, 1 type (s) or 2 or more types can be used arbitrarily from these cationic polymers, and the compounding quantity in hair cosmetics has preferable 0.1 to 10 weight%.

本発明の毛髪化粧料には上記成分以外に、通常化粧料等の製造に使用される添加剤、例えば界面活性剤等の乳化剤、粘度調整剤、pH調整剤、キレート剤、分散媒、軟化剤、紛体、油性成分、油状物質、ポリマー、防腐剤、香料、安定剤、着色剤、紫外線吸収剤、酸化防止剤、保湿剤、抗フケ剤、ビタミン剤、殺菌剤、抗炎症剤等の薬効成分、植物エキス類等を適宜配合し、常法に従って製造することができる。またその際のpHはpH2〜10、特にpH3〜8に調整するのが好ましい。   In addition to the components described above, the hair cosmetic of the present invention includes additives usually used in the production of cosmetics, such as emulsifiers such as surfactants, viscosity modifiers, pH adjusters, chelating agents, dispersion media, and softeners. , Powders, oily ingredients, oily substances, polymers, preservatives, fragrances, stabilizers, colorants, UV absorbers, antioxidants, moisturizers, antidandruff agents, vitamins, bactericides, anti-inflammatory agents, etc. In addition, plant extracts and the like can be appropriately blended and produced according to a conventional method. The pH at that time is preferably adjusted to pH 2 to 10, particularly pH 3 to 8.

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、表1に本明細書記載の方法で合成した毛髪弾力性向上剤1〜4を示した。また表2に毛髪弾力性向上剤の毛髪弾力性向上効果の測定(試験方法1)結果を実施例1〜4及び比較例1〜4に示し、表3に常法により調整したアウトバス用毛髪化粧料を実施例5〜13及び比較例5〜9、表4にインバス用毛髪化粧料を実施例14〜19及び比較例10〜15に示した。毛髪弾力性向上剤並びに毛髪化粧料の毛髪弾力性向上効果の測定(試験方法1、2)は毛髪引張り試験機を用いて確認し、毛髪化粧料の摩擦低減効果(試験方法3、毛髪の滑らかの評価)及び摩耗低減効果(試験方法4、ブラッシング等の摩擦による切れ毛防止の評価)の測定はNRF型摩擦係数計を用いて確認し、また官能評価(試験方法5)よりハリ・コシ感、滑らかさ、ベタツキ感の無さを官能的に評価した結果を示した。含有量は重量%である。   EXAMPLES Next, although an Example demonstrates this invention still in detail, this invention is not limited to an Example. Table 1 shows hair elasticity improvers 1 to 4 synthesized by the method described in this specification. Table 2 shows the results of measurement of the hair elasticity improving effect of hair elasticity improver (Test Method 1) in Examples 1 to 4 and Comparative Examples 1 to 4, and Table 3 shows the hair for out baths adjusted by a conventional method. The cosmetics were shown in Examples 5 to 13 and Comparative Examples 5 to 9, and Table 4 shows the hair cosmetics for invasion in Examples 14 to 19 and Comparative Examples 10 to 15. The hair elasticity improving agent and the measurement of the hair elasticity improving effect of the hair cosmetic (test methods 1 and 2) were confirmed using a hair tension tester, and the friction reducing effect of the hair cosmetic (test method 3, smooth hair) ) And wear reduction effect (Test Method 4, evaluation of prevention of hair breakage due to friction such as brushing) was confirmed using an NRF type friction coefficient meter, and the sense of firmness and firmness from sensory evaluation (Test Method 5) The results of sensory evaluation of smoothness and no stickiness were shown. The content is% by weight.

Figure 0006012394
Figure 0006012394

本実施例中で用いた試験方法は下記の通りである。   The test methods used in this example are as follows.

試験方法1(毛髪弾力性向上剤の毛髪弾力性向上効果の測定)
市販の健康黒髪或いはブリーチ毛(共にビューラックス社製)をpH5クエン酸緩衝溶液中に1時間浸漬後、一晩乾燥(20℃、40%RH)させ、毛髪引張り試験機(カトーテック社製KES−G1−SH)で毛髪破断測定(N=10)をした時の健康黒髪の測定値をA、ブリーチ毛の測定値をBとした。また、実施例1〜4、比較例1〜4で示す溶液に市販のブリーチ毛を1時間浸漬後、一晩乾燥(20℃、40%RH)させ、同様に毛髪破断測定(N=10)をした時の測定値をCとして、次式で毛髪弾力性向上度を計算した。
毛髪弾力性向上度(%)=[(C−B)/(A−B)]×100
また毛髪弾力性向上効果の評価基準は下記の通りである。
(評価基準)
◎:毛髪弾力性向上度が50%以上
○:毛髪弾力性向上度が30%以上50%未満
△:毛髪弾力性向上度が10%以上30%未満
×:毛髪弾力性向上度が10%未満
Test Method 1 (Measurement of hair elasticity improving effect of hair elasticity improving agent)
Commercially available healthy black hair or bleached hair (both manufactured by Beaulux) was immersed in a pH 5 citrate buffer solution for 1 hour, dried overnight (20 ° C., 40% RH), and then a hair tension tester (KES manufactured by Kato Tech Co., Ltd.). The measurement value of healthy black hair when the hair breakage measurement (N = 10) was performed with -G1-SH) was A, and the measurement value of bleached hair was B. Moreover, after immersing a commercially available bleach hair in the solutions shown in Examples 1 to 4 and Comparative Examples 1 to 4 for 1 hour, the hair was dried overnight (20 ° C., 40% RH), and the hair breakage measurement was similarly performed (N = 10). The measured value when the hair was taken was defined as C, and the degree of improvement in hair elasticity was calculated according to the following formula.
Increase in hair elasticity (%) = [(CB) / (AB)] × 100
The evaluation criteria for the effect of improving hair elasticity are as follows.
(Evaluation criteria)
◎: Hair elasticity improvement is 50% or more ○: Hair elasticity improvement is 30% or more and less than 50% △: Hair elasticity improvement is 10% or more and less than 30% ×: Hair elasticity improvement is less than 10%

試験方法2(毛髪化粧料の毛髪弾力性向上効果の測定)
上記試験方法1(毛髪弾力性向上剤の毛髪弾力性向上効果の測定)同様に健康黒髪の測定値をA、ブリーチ毛の測定値をBとした。また、実施例5〜13、比較例5〜9で示すアウトバス用毛髪化粧料を市販のブリーチ毛(ビューラックス社製、20cm×20g)にアトマイザーで1g噴霧、一晩乾燥後、或いは実施例14〜19、比較例10〜15で示すインバス用毛髪化粧料を同様のブリーチ毛に1gを塗布し、すすぎ、一晩乾燥後(上記同条件)、毛髪引張り試験機(カトーテック社製KES−G1−SH)で毛髪破断測定(N=10)した時の測定値をDとし次式で毛髪弾力性向上度を計算した。
毛髪弾力性向上度(%)=[(D−B)/(A−B)]×100
また毛髪弾力性向上効果の評価基準は下記の通りである。
◎:毛髪弾力性向上度が50%以上
○:毛髪弾力性向上度が30%以上50%未満
△:毛髪弾力性向上度が10%以上30%未満
×:毛髪弾力性向上度が10%未満
Test Method 2 (Measurement of hair elasticity improvement effect of hair cosmetics)
Similarly to the above test method 1 (measurement of the hair elasticity improving effect of the hair elasticity improving agent), the measurement value of healthy black hair was A, and the measurement value of bleached hair was B. In addition, the hair cosmetics for out bath shown in Examples 5 to 13 and Comparative Examples 5 to 9 are sprayed on a commercially available bleached hair (Bulux Co., Ltd., 20 cm × 20 g) with an atomizer, dried overnight, or Examples 14-19, 1 g of hair cosmetic for invasion shown in Comparative Examples 10-15 was applied to the same bleached hair, rinsed, dried overnight (same conditions as described above), and then a hair tension tester (KES-Tech, manufactured by Kato Tech Co., Ltd.). The measured value when the hair breakage was measured with G1-SH) (N = 10) was defined as D, and the degree of improvement in hair elasticity was calculated according to the following equation.
Increase in hair elasticity (%) = [(D−B) / (A−B)] × 100
The evaluation criteria for the effect of improving hair elasticity are as follows.
◎: Hair elasticity improvement is 50% or more ○: Hair elasticity improvement is 30% or more and less than 50% △: Hair elasticity improvement is 10% or more and less than 30% ×: Hair elasticity improvement is less than 10%

試験方法3(毛髪化粧料の毛髪摩擦低減効果の測定/滑らかさの評価)
上記試験方法2(毛髪用化粧料の毛髪弾力性向上効果の測定)同様に市販のブリーチ毛を実施例、比較例に示すアウトバス用或いはインバス用毛髪化粧料で処理し、NRF型摩擦係数計(レオロジー機器社製)を用いて荷重40g、回転数3rpm、測定時間5分で動摩擦係数測定(N=10)した時の測定値をEとし、未処理の市販ブリーチ毛を測定した時の測定値をFとして、次式で動摩擦係数低減率を計算した。
動摩擦係数低減率=E/F
また毛髪摩擦低減効果(毛髪の滑らかさ)の評価基準は下記の通りである。
◎:動摩擦係数低減率が0.85以下
○:動摩擦係数低減率が0.85以上0.95未満
△:動摩擦係数低減率が0.95以上1.0未満
×:動摩擦係数低減率が1.0以上
Test Method 3 (Measurement of Hair Friction Reduction Effect of Hair Cosmetic / Evaluation of Smoothness)
Test method 2 (Measurement of hair elasticity improvement effect of cosmetics for hair) Similarly, commercially available bleached hairs were treated with the hair cosmetics for out baths or in baths shown in Examples and Comparative Examples, and NRF type friction coefficient meter (Measured when untreated commercial bleached hair was measured with E as the measured value when the dynamic friction coefficient was measured (N = 10) with a load of 40 g, a rotational speed of 3 rpm, and a measurement time of 5 minutes using Rheological Instruments) Assuming that the value is F, the dynamic friction coefficient reduction rate was calculated by the following equation.
Dynamic friction coefficient reduction rate = E / F
The evaluation criteria for the effect of reducing hair friction (smoothness of hair) are as follows.
◎: Dynamic friction coefficient reduction rate is 0.85 or less ○: Dynamic friction coefficient reduction rate is 0.85 or more and less than 0.95 Δ: Dynamic friction coefficient reduction rate is 0.95 or more and less than 1.0 ×: Dynamic friction coefficient reduction rate is 1. 0 or more

試験方法4(毛髪用化粧料の毛髪摩耗低減効果の測定/切れ毛防止の評価)
上記試験方法3(毛髪用化粧料の毛髪摩擦低減効果の測定)同様に処理したブリーチ毛をNRF型摩擦係数計(レオロジー機器社製)を用いて荷重100g、回転数200rpmの負荷条件で破断するまでの時間を測定(N=10)し、毛髪摩耗低減効果(ブラッシング等の摩擦による切れ毛防止)を評価した。評価基準は下記の通りである。
◎:破断時間が600秒以上
○:破断時間が480秒以上600秒未満
△:破断時間が360秒以上480秒未満
×:破断時間が360秒以下
Test Method 4 (Measurement of Hair Wear Reduction Effect of Hair Cosmetic / Evaluation of Cut Hair Prevention)
The bleached hair treated in the same manner as in the above test method 3 (measurement of the effect of reducing hair friction of hair cosmetics) is broken using an NRF friction coefficient meter (manufactured by Rheology Equipment Co., Ltd.) under a load condition of 100 g load and 200 rpm rotation speed. Was measured (N = 10), and the hair wear reduction effect (prevention of hair breakage due to friction such as brushing) was evaluated. The evaluation criteria are as follows.
◎: Break time 600 seconds or more ○: Break time 480 seconds or more and less than 600 seconds Δ: Break time 360 seconds or more and less than 480 seconds X: Break time 360 seconds or less

試験方法5(毛髪化粧料の使用性の評価(ハリ・コシ感、滑らかさ、ベタツキ感の無さ))
上記試験方法3(毛髪用化粧料の毛髪摩擦低減効果の測定)同様に処理したブリーチ毛を10名の専門パネラーにより「ハリ・コシ感、滑らかさ、ベタツキ感の無さ」の評価を官能的に行った。評価基準は下記の通りである。
◎:良いと答えた人が9人以上の場合
○:良いと答えた人が6〜8人の場合
△:良いと答えた人が3〜5人の場合
×:良いと答えた人が2人以下の場合
Test Method 5 (Evaluation of Usability of Hair Cosmetics (No firmness, firmness, smoothness, stickiness))
Test method 3 (Measurement of hair friction reduction effect of cosmetics for hair) 10 expert panelists evaluated the "no firmness, smoothness, and stickiness" evaluation by 10 expert panelists. Went to. The evaluation criteria are as follows.
◎: When there are more than 9 people who answered good ○: When there are 6-8 people who answered good △: When there are 3-5 people who answered good ×: 2 people who answered good For people below

Figure 0006012394
Figure 0006012394

Figure 0006012394
Figure 0006012394

Figure 0006012394
Figure 0006012394

実施例1〜19及び比較例1〜15より明らかなように、本発明のタウリン誘導体、並びにタウリン誘導体を含有する毛髪化粧料は、毛髪弾力性向上効果、摩擦低減効果(毛髪の滑らかの評価)、摩耗低減効果(ブラッシング等の摩擦による切れ毛防止の評価)、使用性(官能評価:ハリ・コシ感、滑らかさ、ベタツキ感の無さ)で優れた性能を示した。   As is clear from Examples 1 to 19 and Comparative Examples 1 to 15, the taurine derivative of the present invention and the hair cosmetic containing the taurine derivative have an effect of improving hair elasticity and an effect of reducing friction (evaluation of smoothness of hair). Excellent performance in wear reduction effect (evaluation of prevention of hair breakage due to friction such as brushing) and usability (sensory evaluation: firmness, firmness, smoothness, no stickiness).

上記記載のごとく、本発明の毛髪弾力性向上剤並びに毛髪弾力性向上剤を含有する毛髪化粧料は、日常での物理的、化学的作用により損傷を受けた毛髪に優れた弾力性向上効果と良好な使用性(ハリ・コシ感、滑らかさ、ベタツキ感の無さ)を与えることは明らかである。
As described above, the hair elasticity improver of the present invention and the hair cosmetic containing the hair elasticity improver are excellent in improving elasticity to hair damaged by daily physical and chemical actions. It is clear that it gives good usability (harshness, firmness, smoothness, no stickiness).

Claims (3)

下記一般式(1)
Figure 0006012394
(式中、R、Rのいずれか一方/又は両方は、下記一般式(2)で表される基、残りは水素原子を表し、Mは水素原子、アルカリ金属、アルカリ土類金属、アンモニウム及び有機アミンから選ばれる少なくとも1種を表す。)
Figure 0006012394
(式中、Rは直鎖又は分岐した炭素数1〜8のアルキル基、アルケニル基もしくはヒドロキシアルキル基)
で表されるタウリン誘導体からなる毛髪弾力性向上剤。
The following general formula (1)
Figure 0006012394
(In the formula, either one or both of R 1 and R 2 are groups represented by the following general formula (2), the rest represent a hydrogen atom, M is a hydrogen atom, an alkali metal, an alkaline earth metal, It represents at least one selected ammonium and organic Amin or al.)
Figure 0006012394
(Wherein R 3 is a linear or branched alkyl group having 1 to 8 carbon atoms, an alkenyl group or a hydroxyalkyl group)
A hair elasticity improving agent comprising a taurine derivative represented by the formula:
請求項1記載の毛髪弾力性向上剤を含有する毛髪化粧料。 A hair cosmetic containing the hair elasticity improving agent according to claim 1. 毛髪の弾力性を回復する効果を目的とする請求項2記載の毛髪化粧料。 The hair cosmetic composition according to claim 2, which has an effect of restoring the elasticity of the hair.
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