JP2001294519A - Hair dye composition - Google Patents
Hair dye compositionInfo
- Publication number
- JP2001294519A JP2001294519A JP2000113305A JP2000113305A JP2001294519A JP 2001294519 A JP2001294519 A JP 2001294519A JP 2000113305 A JP2000113305 A JP 2000113305A JP 2000113305 A JP2000113305 A JP 2000113305A JP 2001294519 A JP2001294519 A JP 2001294519A
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- JP
- Japan
- Prior art keywords
- group
- red
- hair
- dyes
- acid
- 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.)
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- Coloring (AREA)
Abstract
(57)【要約】
【解決手段】 (A)蛍光増白染料及び(B)直接染料
を含有する染毛剤組成物。
【効果】 本発明染毛剤組成物を用いれば、染色後の毛
髪が明るく、かつあざやかになる。(57) Abstract: A hair dye composition containing (A) a fluorescent whitening dye and (B) a direct dye. [Effect] By using the hair dye composition of the present invention, the hair after dyeing becomes bright and vivid.
Description
【0001】[0001]
【発明の属する技術分野】本発明は、明るく、あざやか
な色に染めることのできる染毛剤組成物に関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a hair dye composition capable of dyeing a bright, bright color.
【0002】[0002]
【従来の技術及び発明が解決しようとする課題】一般に
直接染料を用いる染毛剤の場合には、明るくあざやかな
色に染めることができないという欠点があった。更に染
料が色落ちしやすいという欠点もあった。また市販のつ
や出し剤を併用した場合でもつやは出るが、毛髪の色を
明るくあざやかにはできなかった。2. Description of the Related Art Generally, a hair dye using a direct dye has a disadvantage that it cannot be dyed into a bright and vivid color. Further, there is a disadvantage that the dye is easily discolored. Further, when a commercially available polishing agent is used in combination, the hair becomes shiny, but the hair color cannot be made bright and vivid.
【0003】[0003]
【課題を解決するための手段】そこで本発明者は、直接
染料による染毛効果を向上させるべく種々検討した結
果、直接染料に、それ自体は無色である蛍光増白染料を
組み合せれば、全く意外にも明るく、あざやかな色に染
めることができ、同時に色落ちしにくい染毛剤が得られ
ることを見出した。The present inventor has made various studies to improve the hair dyeing effect of the direct dye. As a result, if the direct dye is combined with a colorless fluorescent whitening dye itself, the direct dye is completely eliminated. It has been found that a hair dye which can be dyed in a surprisingly bright and brilliant color and at the same time hardly loses color is obtained.
【0004】すなわち、本発明は(A)蛍光増白染料及
び(B)直接染料を含有する染毛剤組成物を提供するも
のである。That is, the present invention provides a hair dye composition containing (A) a fluorescent whitening dye and (B) a direct dye.
【0005】[0005]
【発明の実施の形態】本発明に用いられる(A)蛍光増
白染料とは、近紫外部(330〜380nm)の光を吸
収し、可視部の短波長領域(400〜450nm)に紫
ないし青色の蛍光を発する白色ないし淡黄色染料であ
り、これ自体では無色に見えるものである。当該蛍光増
白染料の化粧料への応用例としては、毛髪への光沢付与
方法(特開平9−183714号)や髪に光沢を与える
ためのシャンプー(特公昭48−17362号)等があ
るが、染毛剤への応用例、ひいては直接染料との組み合
せによりいかなる作用が出現するかについては全く知ら
れていない。BEST MODE FOR CARRYING OUT THE INVENTION The fluorescent brightening dye (A) used in the present invention absorbs near-ultraviolet (330 to 380 nm) light and emits ultraviolet light in the short wavelength region (400 to 450 nm) of the visible region. It is a white to pale yellow dye that emits blue fluorescence and appears colorless by itself. Examples of the application of the fluorescent whitening dye to cosmetics include a method for imparting gloss to hair (Japanese Patent Application Laid-Open No. 9-183714) and a shampoo for imparting gloss to hair (Japanese Patent Publication No. 48-17362). No application is known for hair dyes, and no effect whatsoever is exhibited by combination with direct dyes.
【0006】(A)蛍光増白染料としては、ジスチルビ
フェニリルやトリアジニルアミノスチルベン系等のスチ
ルベン誘導体、ベンゾオキサゾール誘導体、ナフタルイ
ミド誘導体、ベンズイミダゾール誘導体、ピラゾリン誘
導体、クマリン誘導体等が挙げられる。市販品として
は、チノパールCBS−X、チノパールMSP、ユビテ
ックスBHT、ユビテックスNFW450%、ユビテッ
クス2B(チバスペシャルティケミカルス社製)等のス
チルベン誘導体;チノパールAMS−GX、チノパール
5BM−GX、チノパールUNPA−GX(チバスペシ
ャルティケミカルス社製)等のトリアジニルアミノスチ
ルベン誘導体;ユビテックスWG−01(チバスペシャ
ルティケミカルス社製)等のピラゾリン誘導体;ユビテ
ックスBAC(チバスペシャルティケミカルス社製)等
のカチオン化イミダゾール誘導体;ユビテックスEM
T、ユビテックスEBF250%(チバスペシャルティ
ケミカルス社製)等のオキサゾールやピレン誘導体;チ
ノパールSWN(チバスペシャルティケミカルス社製)
等のクマリン誘導体が挙げられる。(A) Examples of the fluorescent whitening dye include stilbene derivatives such as distilbiphenylyl and triazinylaminostilbene, benzoxazole derivatives, naphthalimide derivatives, benzimidazole derivatives, pyrazoline derivatives, and coumarin derivatives. . Commercially available products include stilbene derivatives such as Tinopearl CBS-X, Tinopearl MSP, Ubitex BHT, Ubitex NFW450%, Ubitex 2B (manufactured by Ciba Specialty Chemicals); Tinopearl AMS-GX, Tinopearl 5BM-GX, Tinopearl UNPA- Triazinylaminostilbene derivatives such as GX (manufactured by Ciba Specialty Chemicals); pyrazoline derivatives such as Ubitex WG-01 (manufactured by Ciba Specialty Chemicals); cationized imidazole derivatives such as Ubitex BAC (manufactured by Ciba Specialty Chemicals) ; Ubitex EM
Oxazole and pyrene derivatives such as T, Ubitex EBF 250% (manufactured by Ciba Specialty Chemicals); Tinopearl SWN (manufactured by Ciba Specialty Chemicals)
And the like.
【0007】これらの(A)蛍光増白染料は、2種以上
を用いるこもでき、染め上がりの明るさ、あざやかさの
点から、本発明染毛剤組成中に合計で0.001〜5重
量%、特に0.005〜4重量%、更に0.01〜4重
量%含有させるのが好ましい。Two or more of these (A) fluorescent whitening dyes can be used, and from the viewpoint of lightness of dyeing and brilliancy, a total of 0.001 to 5% by weight in the hair dye composition of the present invention. In particular, the content is preferably 0.005 to 4% by weight, more preferably 0.01 to 4% by weight.
【0008】本発明染毛剤組成物に用いられる成分
(B)の直接染料としては、ニトロ染料、キノン染料、
アゾ染料、アジン染料、アクリジン染料、オキサジン染
料、トリフェニルメタン染料、キノリン染料、ザンセン
染料、インジゴイド染料、スチルベン染料、チアゾール
染料、更に天然染料等が挙げられる。これらのうち、酸
性染料又は塩基性染料が、非イオン性の染料に比べ、染
色性及び堅牢性の点から好ましい。The direct dye of the component (B) used in the hair dye composition of the present invention includes nitro dyes, quinone dyes,
Examples include azo dyes, azine dyes, acridine dyes, oxazine dyes, triphenylmethane dyes, quinoline dyes, xansen dyes, indigoid dyes, stilbene dyes, thiazole dyes, and natural dyes. Among these, acid dyes or basic dyes are preferable from the viewpoint of dyeability and fastness as compared with nonionic dyes.
【0009】酸性染料としては、例えば赤色2号(C.I.
16185)、赤色3号(C.I.45430)、赤色102号(C.I.
16255)、赤色104号の(1)(C.I.45410)、赤色1
05号の(1)(C.I.45440)、赤色106号(C.I.451
00)、黄色4号(C.I.19140)、黄色5号(C.I.1598
5)、緑色3号(C.I.42053)、青色1号(C.I.4209
0)、青色2号(C.I.73015)、赤色201号(C.I.1585
0)、赤色227号(C.I.17200)、赤色230号の
(1)(C.I.45380)、赤色231号(C.I.45410)、赤
色232号(C.I.45440)、だいだい色205号(C.I.1
5510)、だいだい色207号(C.I.45425)、黄色20
2号の(1)(C.I.45350)、黄色203号(C.I.4700
5)、緑色201号(C.I.61570)、緑色204号(C.I.
59040)、緑色205号(C.I.42095)、青色202号
(C.I.42052)、青色205号(C.I.42090)、かっ色2
01号(C.I.20170)、赤色401号(C.I.45190)、赤
色502号(C.I.16155)、赤色503号(C.I.1615
0)、赤色504号(C.I.14700)、赤色506号(C.I.
15620)、だいだい色402号(C.I.14600)、黄色40
2号(C.I.18950)、黄色403号の(1)(C.I.1031
6)、黄色406号(C.I.13065)、黄色407号(C.I.
18820)、緑色401号(C.I.10020)、緑色402号
(C.I.42085)、紫色401号(C.I.60730)、黒色40
1号(C.I.20470)、アシッドブラック52(C.I.1571
1)、アシッドブルー1(C.I.42045)、アシッドブルー
3(C.I.42051)、アシッドブルー62(C.I.62045)、
アシッドブラウン13(C.I.10410)、アシッドグリー
ン50(C.I.44090)、アシッドオレンジ3(C.I.1038
5)、アシッドオレンジ6(C.I.14270)、アシッドレッ
ド14(C.I.14720)、アシッドレッド35(C.I.1806
5)、アシッドレッド73(C.I.27290)、アシッドレッ
ド184(C.I.15685)、ブリリアントブラック1(C.
I.28440)等が挙げられる。As the acid dye, for example, Red No. 2 (CI
16185), Red No. 3 (CI45430), Red No. 102 (CI
16255), Red No. 104 (1) (CI45410), Red 1
No. 05 (1) (CI45440), Red No. 106 (CI451
00), Yellow No. 4 (CI19140), Yellow No. 5 (CI1598)
5), Green No. 3 (CI42053), Blue No. 1 (CI4209)
0), Blue No. 2 (CI73015), Red No. 201 (CI1585
0), red 227 (CI17200), red 230 (1) (CI45380), red 231 (CI45410), red 232 (CI45440), orange color 205 (CI1)
5510), orange color 207 (CI45425), yellow 20
No. 2 (1) (CI45350), Yellow No. 203 (CI4700
5), Green No. 201 (CI61570), Green No. 204 (CI
59040), Green No. 205 (CI42095), Blue No. 202 (CI42052), Blue No. 205 (CI42090), Brown 2
01 (CI20170), Red 401 (CI45190), Red 502 (CI16155), Red 503 (CI1615)
0), Red No. 504 (CI14700), Red No. 506 (CI
15620), orange color 402 (CI14600), yellow 40
No. 2 (CI18950), Yellow No. 403 (1) (CI1031
6), Yellow No. 406 (CI13065), Yellow No. 407 (CI
18820), green 401 (CI10020), green 402 (CI42085), purple 401 (CI60730), black 40
No. 1 (CI20470), Acid Black 52 (CI1571)
1), Acid Blue 1 (CI42045), Acid Blue 3 (CI42051), Acid Blue 62 (CI62045),
Acid Brown 13 (CI10410), Acid Green 50 (CI44090), Acid Orange 3 (CI1038)
5), Acid Orange 6 (CI14270), Acid Red 14 (CI14720), Acid Red 35 (CI1806)
5), Acid Red 73 (CI27290), Acid Red 184 (CI15685), Brilliant Black 1 (C.
I.28440).
【0010】塩基性染料としては、例えばベーシックブ
ルー7(C.I.42595)、ベーシックブルー26(C.I.440
45)、ベーシックブルー99(C.I.56059)、ベーシッ
クバイオレット10(C.I.45170)、ベーシックバイオ
レット14(C.I.42515)、ベーシックブラウン16
(C.I.12250)、ベーシックブラウン17(C.I.1225
1)、ベーシックレッド2(C.I.50240)、ベーシックレ
ッド22(C.I.11055)、ベーシックレッド76(C.I.1
2245)、ベーシックレッド118(C.I.12251:1)、ベ
ーシックイエロー57(C.I.12719);特公昭58-2204
号、特開平9-118832号等に記載されている、芳香環の側
鎖に4級化窒素原子を含有する塩基性染料;特表平10-5
02946号、特開平10-182379号等に記載されている、次式
で表わされる、非局在化していても良い4級化窒素原子
及び−Z=N−結合(Zは窒素原子又は−CH−基を示
す)を含有する塩基性染料などが挙げられる。As basic dyes, for example, Basic Blue 7 (CI42595) and Basic Blue 26 (CI440)
45), Basic Blue 99 (CI56059), Basic Violet 10 (CI45170), Basic Violet 14 (CI42515), Basic Brown 16
(CI12250), Basic Brown 17 (CI1225
1), Basic Red 2 (CI50240), Basic Red 22 (CI11055), Basic Red 76 (CI1
2245), Basic Red 118 (CI12251: 1), Basic Yellow 57 (CI12719);
And basic dyes containing a quaternized nitrogen atom in the side chain of an aromatic ring, as described in JP-A No. 9-118832 and JP-A-9-18832;
02946, JP-A-10-182379, etc., represented by the following formula, optionally quaternized nitrogen atom and -Z = N- bond (Z is a nitrogen atom or -CH -Indicating a group).
【0011】[0011]
【化5】 Embedded image
【0012】また、酸性染料及び塩基性染料以外の直接
染料としては、例えば2−アミノ−3−ニトロフェノー
ル、2−アミノ−4−ニトロフェノール、2−アミノ−
5−ニトロフェノール、4−アミノ−3−ニトロフェノ
ール、2−アミノ−6−クロロ−4−ニトロフェノー
ル、4−ヒドロキシプロピルアミノ−3−ニトロフェノ
ール、3−ニトロパラヒドロキシエチルアミノフェノー
ル、2−ニトロパラフェニレンジアミン、4−ニトロオ
ルトフェニレンジアミン、4−ニトロメタフェニレンジ
アミン、6−ニトロオルトトルイジン、6−ニトロパラ
トルイジン、ヒドロキシエチル−2−ニトロパラトルイ
ジン、N,N’−ビス(2−ヒドロキシエチル)−2−
ニトロパラフェニレンジアミン、2−クロロ−5−ニト
ロ−N−ヒドロキシエチルパラフェニレンジアミン、2
−ニトロ−5−グリセリルメチルアニリン、3−メチル
アミノ−4−ニトロフェノキシエタノール、N−エチル
−3−ニトロPABA、ピクラミン酸、2−ヒドロキシ
エチルピクラミン酸、4−ニトロフェニルアミノエチル
ウレア、紫色201号(C.I.60725)、ソルベントイエ
ロー44(C.I.56200)、ディスパーズレッド17(C.
I.11210)、ディスパーズバイオレット1(C.I.6110
0)、ディスパーズバイオレット4(C.I.61105)ディス
パーズブルー3(C.I.61505)、ディスパーズブルー7
(C.I.62500)、HCブルーNo.2、HCブルーNo.8、
HCオレンジNo.1、HCオレンジNo.2、HCレッドN
o.1、HCレッドNo.3、HCレッドNo.7 、HCレッ
ドNo.8、HCレッドNo.10、HCレッドNo.11、H
CレッドNo.13、HCレッドNo.16、HCバイオレッ
トNo.2、HCイエローNo.2、HCイエローNo.5、H
CイエローNo.6、HCイエローNo.7、HCイエローN
o.9、HCイエローNo.12等が挙げられる。The direct dyes other than the acid dyes and the basic dyes include, for example, 2-amino-3-nitrophenol, 2-amino-4-nitrophenol, 2-amino-
5-nitrophenol, 4-amino-3-nitrophenol, 2-amino-6-chloro-4-nitrophenol, 4-hydroxypropylamino-3-nitrophenol, 3-nitroparahydroxyethylaminophenol, 2-nitro Paraphenylenediamine, 4-nitroorthophenylenediamine, 4-nitrometaphenylenediamine, 6-nitroorthotoluidine, 6-nitroparatoluidine, hydroxyethyl-2-nitroparatoluidine, N, N'-bis (2-hydroxyethyl ) -2-
Nitroparaphenylenediamine, 2-chloro-5-nitro-N-hydroxyethylparaphenylenediamine, 2
-Nitro-5-glycerylmethylaniline, 3-methylamino-4-nitrophenoxyethanol, N-ethyl-3-nitroPABA, piclamic acid, 2-hydroxyethylpiclamic acid, 4-nitrophenylaminoethylurea, purple No. 201 (CI60725), Solvent Yellow 44 (CI56200), Disperse Red 17 (C.
I.11210), Disperse Violet 1 (CI6110
0), Disperse Violet 4 (CI61105) Disperse Blue 3 (CI61505), Disperse Blue 7
(CI62500), HC Blue No. 2, HC Blue No. 8,
HC Orange No.1, HC Orange No.2, HC Red N
o.1, HC Red No.3, HC Red No.7, HC Red No.8, HC Red No.10, HC Red No.11, H
C Red No. 13, HC Red No. 16, HC Violet No. 2, HC Yellow No. 2, HC Yellow No. 5, H
C Yellow No. 6, HC Yellow No. 7, HC Yellow N
o.9, HC Yellow No.12, and the like.
【0013】成分(B)の直接染料は、2種以上を用い
ることもでき、染毛剤組成物中の含有量は、所望の染毛
力等により異なるが、全組成中に合計で0.001〜5
重量%、特に0.005〜5重量%、更に0.01〜4
重量%含有させるのが好ましい。Two or more direct dyes of component (B) can be used. The content of the direct dye in the hair dye composition varies depending on the desired hair dyeing power and the like. 001-5
% By weight, particularly 0.005 to 5% by weight, further 0.01 to 4% by weight
It is preferable that the content is contained by weight.
【0014】本発明染毛剤組成物には、染毛効果及び明
るさやあざやかさを更に向上させる目的で、浸透促進溶
剤、特に(C)一般式(1)〜(4)で表わされる化合
物から選択される1種以上の化合物を含有させるのが好
ましい。The hair dye composition of the present invention comprises a solvent for promoting penetration, particularly (C) a compound represented by the general formula (1) to (4), for the purpose of further improving the hair dyeing effect and the brightness and brilliancy. It is preferred to include one or more selected compounds.
【0015】[0015]
【化6】 Embedded image
【0016】(式中、R1は水素原子、メチル基又はメ
トキシ基を示し、R2は単結合、メチレン基又エチレン
基を示し、R3は水素原子、メチル基又はエチル基を示
し、aは0〜2の整数を示す)Wherein R 1 represents a hydrogen atom, a methyl group or a methoxy group; R 2 represents a single bond, a methylene group or an ethylene group; R 3 represents a hydrogen atom, a methyl group or an ethyl group; Represents an integer of 0 to 2)
【0017】[0017]
【化7】 Embedded image
【0018】(式中、R4は水素原子、メチル基又はエ
チル基を示し、R5は炭素数1〜4の直鎖又は分岐鎖の
アルキル基を示し、R6は水素原子又は炭素数1〜4の
直鎖又は分岐鎖のアルキル基を示し、bは1〜3の整数
を示す)(Wherein, R 4 represents a hydrogen atom, a methyl group or an ethyl group, R 5 represents a linear or branched alkyl group having 1 to 4 carbon atoms, and R 6 represents a hydrogen atom or 1 carbon atom. Represents a straight-chain or branched-chain alkyl group of 4 to 4, and b represents an integer of 1 to 3.)
【0019】[0019]
【化8】 Embedded image
【0020】(式中、R7は炭素数1〜18の直鎖又は
分岐鎖のアルキル基を示す)(Wherein, R 7 represents a linear or branched alkyl group having 1 to 18 carbon atoms)
【0021】[0021]
【化9】 Embedded image
【0022】(式中、R8は水素原子、メチル基又はエ
チル基を示す)。(Wherein, R 8 represents a hydrogen atom, a methyl group or an ethyl group).
【0023】本発明で用いる成分(C)の化合物のう
ち、一般式(1)で表わされるものとしては、ベンジル
アルコール、2−ベンジルオキシエタノール等が挙げら
れる。一般式(2)中、R5及びR6のアルキル基として
は、メチル基、エチル基等が挙げられる。化合物(2)
としては、2−n−ブトキシエタノール、ジプロピレン
グリコールジエチルエーテル等が挙げられる。一般式
(3)中、R7としては、メチル基、エチル基、n−プ
ロピル基等の炭素数1〜6のアルキル基が好ましく、化
合物(3)としては、N−メチル−2−ピロリドン等が
挙げられる。一般式(4)としては、プロピレンカーボ
ネート等が挙げられる。Among the compounds of the component (C) used in the present invention, those represented by the general formula (1) include benzyl alcohol, 2-benzyloxyethanol and the like. In the general formula (2), examples of the alkyl group of R 5 and R 6 include a methyl group and an ethyl group. Compound (2)
Examples thereof include 2-n-butoxyethanol and dipropylene glycol diethyl ether. In the general formula (3), R 7 is preferably an alkyl group having 1 to 6 carbon atoms such as a methyl group, an ethyl group, and an n-propyl group, and the compound (3) is N-methyl-2-pyrrolidone or the like. Is mentioned. Examples of the general formula (4) include propylene carbonate.
【0024】成分(C)の化合物は2種以上を用いるこ
ともでき、全組成中に合計で0.5〜50重量%、特に
1〜40重量%、更に、5〜30重量%含有させるのが
好ましい。Two or more compounds of the component (C) can be used. The total content of the compounds is 0.5 to 50% by weight, preferably 1 to 40% by weight, and more preferably 5 to 30% by weight. Is preferred.
【0025】本発明染毛剤組成物には、塗布性、操作性
等を向上させる目的で(D)水溶性高分子を含有させる
のが好ましい。当該(D)水溶性高分子としては、グア
ーガム、ローカストビーンガム、カラギーナン、カラヤ
ガム、アラビアガム、トラガロントガム、キサンタンガ
ム等の天然高分子;ヒドロキシエチルセルロース、ヒド
ロキシプロピルセルロース、カルボキシメチルセルロー
ス等のセルロース系高分子;ポリビニルアルコール、ポ
リビニルピロリドン、ポリアクリル酸ナトリウム、カル
ボキシビニルポリマー等の合成高分子;アルキレンオキ
シド変性キサンタンガム等が挙げられる。このうち、ヒ
ドロキシエチルセルロース、キサンタンガム、アルキレ
ンオキシド変性キサンタンガムが特に好ましい。The hair dye composition of the present invention preferably contains (D) a water-soluble polymer for the purpose of improving applicability, operability and the like. Examples of the (D) water-soluble polymer include natural polymers such as guar gum, locust bean gum, carrageenan, karaya gum, arabic gum, tragalont gum, and xanthan gum; cellulose-based polymers such as hydroxyethyl cellulose, hydroxypropyl cellulose, and carboxymethyl cellulose; Synthetic polymers such as alcohol, polyvinylpyrrolidone, sodium polyacrylate, and carboxyvinyl polymer; and alkylene oxide-modified xanthan gum. Among them, hydroxyethyl cellulose, xanthan gum and alkylene oxide-modified xanthan gum are particularly preferred.
【0026】これらの(D)水溶性高分子は2種以上を
用いることもでき、合計で染毛剤組成物の粘度を100
0〜50000mPa・sとする量、特に0.1〜10
重量%、更に0.5〜5重量%含有させるのが好まし
い。Two or more of these (D) water-soluble polymers can be used, and the total viscosity of the hair dye composition is 100%.
0 to 50000 mPa · s, especially 0.1 to 10
% By weight, more preferably 0.5 to 5% by weight.
【0027】本発明の染毛剤組成物のpHは、成分
(B)として主に酸性染料を用いる場合にはpH2〜
6、特にpH2.5〜4が好ましく、成分(B)として
主に塩基性染料を用いる場合には、pH6〜11、特に
pH7〜10が好ましい。pHがこれらの範囲であれ
ば、十分な染色効果が得られるとともに、皮膚への刺激
の問題もなく好ましい。これらのpHの調整は、クエン
酸、グリコール酸、コハク酸、酒石酸、乳酸、フマル
酸、リンゴ酸等の有機酸;リン酸、塩酸、 等の無
機酸、水酸化ナトリウム、水酸化カリウム、アンモニア
等のアルカリを適宜組み合せて行うのが好ましい。The pH of the hair dye composition of the present invention may be pH 2 to 2 when an acid dye is mainly used as the component (B).
6, particularly preferably 2.5 to 4, and when a basic dye is mainly used as the component (B), the pH is preferably 6 to 11, particularly preferably 7 to 10. When the pH is within these ranges, a sufficient dyeing effect can be obtained, and there is no problem of irritation to the skin. Adjustment of these pHs is performed by using organic acids such as citric acid, glycolic acid, succinic acid, tartaric acid, lactic acid, fumaric acid, and malic acid; inorganic acids such as phosphoric acid and hydrochloric acid; sodium hydroxide, potassium hydroxide, and ammonia. It is preferable to carry out the reaction by appropriately combining the alkalis.
【0028】本発明の染毛剤組成物には、前記成分のほ
か、通常の化粧品等に用いられる成分、例えば界面活性
剤、カチオン性重合体、低級アルコール、ポリオール、
油性成分、シリコーン誘導体、防腐剤、紫外線吸収剤、
酸化防止剤、殺菌剤、噴射剤等を、適宜配合でき、通常
の方法に従って製造され、非酸化型の染毛剤組成物とす
ることができる。その形態としては、ジェルタイプ、液
状タイプ、ムースタイプ等が挙げられる。The hair dye composition of the present invention contains, in addition to the above components, components used in ordinary cosmetics and the like, such as surfactants, cationic polymers, lower alcohols, polyols,
Oily components, silicone derivatives, preservatives, UV absorbers,
An antioxidant, a bactericide, a propellant, and the like can be appropriately compounded and produced according to a usual method to obtain a non-oxidative hair dye composition. Examples of the form include a gel type, a liquid type, and a mousse type.
【0029】本発明の染毛剤組成物を使用するには、例
えば櫛やブラシ等に適量を受け取って頭髪に塗布し、塗
布後1〜30分間程度放置してから洗い流せば良い。In order to use the hair dye composition of the present invention, for example, an appropriate amount is received by a comb or a brush and applied to the hair, left for about 1 to 30 minutes after application, and then washed off.
【0030】[0030]
【実施例】実施例1 表1に示す染毛剤組成物を常法により製造した。得られ
た組成物2gをヤギ毛1gに均一に塗布し、25℃の室
内で15分間放置した後、濯ぎ流し、次いで表2の組成
のシャンプーで洗浄し、乾燥した。このヤギ毛について
L値、a値、b値を、色彩色差計(ミノルタ CR−3
00)を用いて測定した。EXAMPLES Example 1 Hair dye compositions shown in Table 1 were produced by a conventional method. 2 g of the obtained composition was uniformly applied to 1 g of goat hair, left in a room at 25 ° C. for 15 minutes, rinsed, then washed with a shampoo having the composition shown in Table 2, and dried. The L value, a value, and b value of this goat hair were measured using a colorimeter (Minolta CR-3).
00).
【0031】また専門パネラー10名による色の評価を
行い、色が明るく鮮やか:5点、色がやや明るく、鮮や
か:3点、色が暗くくすむ:1点とし、評価を行った。
この平均点4点以上を◎、2.5点以上を○、2.4点
以下を△とし、パネラー評価を記入した。得られた結果
を表1に示す。The color was evaluated by 10 professional panelists, and the evaluation was made as 5 points for bright and vivid colors, 3 points for slightly bright and vivid colors, and 3 points for dark colors.
The average score of 4 or more was rated as ◎, the score of 2.5 or more was rated as ○, and the score of 2.4 or less was rated as Δ. Table 1 shows the obtained results.
【0032】[0032]
【表1】 [Table 1]
【0033】[0033]
【表2】 [Table 2]
【0034】表1より、直接染料に蛍光増白染料を併用
すると、直接染料単独の場合に比べて、明るさを示す基
準ΔEが顕著に増大し、飛躍的に色が明るくなっている
ことがわかる。更に、明るさが向上したことに伴い、色
があざやかに見える効果が得られることがわかった。From Table 1, it can be seen that when the fluorescent whitening dye is used in combination with the direct dye, the reference ΔE indicating the brightness is significantly increased as compared with the case where the direct dye is used alone, and the color is dramatically increased. Understand. Further, it was found that the effect of making the color look vivid was obtained with the improvement in brightness.
【0035】このヤギ毛を、更に、表2に示すシャンプ
ー(2.5g)で洗浄を5回行い、乾燥した。このヤギ
毛についてL値、a値、b値を上記と同様に測定した。
その結果、表3に示すように、本発明品1は色落ちしに
くいことがわかった。The goat hair was further washed five times with a shampoo (2.5 g) shown in Table 2 and dried. The L value, a value, and b value of this goat hair were measured in the same manner as described above.
As a result, as shown in Table 3, it was found that the product 1 of the present invention hardly discolored.
【0036】[0036]
【表3】 [Table 3]
【0037】[0037]
【発明の効果】本発明染毛剤組成物を用いれば、染色後
の毛髪が明るく、かつあざやかになる。According to the hair dye composition of the present invention, the hair after dyeing becomes bright and vivid.
───────────────────────────────────────────────────── フロントページの続き Fターム(参考) 4C083 AB032 AC032 AC102 AC171 AC302 AC792 AC841 AC842 AC851 AC852 AD162 AD282 BB21 CC36 DD23 EE06 EE07 EE26 4H057 AA01 BA01 BA02 BA03 BA04 CA37 CB16 CB19 CB27 CC02 DA01 DA21 ──────────────────────────────────────────────────続 き Continued on the front page F term (reference) 4C083 AB032 AC032 AC102 AC171 AC302 AC792 AC841 AC842 AC851 AC852 AD162 AD282 BB21 CC36 DD23 EE06 EE07 EE26 4H057 AA01 BA01 BA02 BA03 BA04 CA37 CB16 CB19 CB27 CC02 DA01 DA21
Claims (3)
を含有する染毛剤組成物。A hair dye composition comprising (A) a fluorescent whitening dye and (B) a direct dye.
染料から選ばれる1種又は2種以上である請求項1記載
の染毛剤組成物。2. The hair dye composition according to claim 1, wherein (B) the direct dye is one or more selected from acid dyes and basic dyes.
される化合物から選択される1種以上の化合物を含有す
るものである請求項1又は2記載の染毛剤組成物。 【化1】 (式中、R1は水素原子、メチル基又はメトキシ基を示
し、R2は単結合、メチレン基又エチレン基を示し、R3
は水素原子、メチル基又はエチル基を示し、aは0〜2
の整数を示す) 【化2】 (式中、R4は水素原子、メチル基又はエチル基を示
し、R5は炭素数1〜4の直鎖又は分岐鎖のアルキル基
を示し、R6は水素原子又は炭素数1〜4の直鎖又は分
岐鎖のアルキル基を示し、bは1〜3の整数を示す) 【化3】 (式中、R7は炭素数1〜18の直鎖又は分岐鎖のアル
キル基を示す) 【化4】 (式中、R8は水素原子、メチル基又はエチル基を示
す)。3. The hair dye composition according to claim 1, further comprising (C) one or more compounds selected from the compounds represented by formulas (1) to (4). Embedded image (Wherein, R 1 represents a hydrogen atom, a methyl group or a methoxy group, R 2 is a single bond, represents a methylene group or ethylene group, R 3
Represents a hydrogen atom, a methyl group or an ethyl group;
The following is an integer: (Wherein, R 4 represents a hydrogen atom, a methyl group or an ethyl group, R 5 represents a linear or branched alkyl group having 1 to 4 carbon atoms, and R 6 represents a hydrogen atom or a 1 to 4 carbon atoms. Represents a linear or branched alkyl group, and b represents an integer of 1 to 3.) (Wherein, R 7 represents a linear or branched alkyl group having 1 to 18 carbon atoms). (Wherein, R 8 represents a hydrogen atom, a methyl group or an ethyl group).
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2000113305A JP4162355B2 (en) | 2000-04-14 | 2000-04-14 | Hair dye composition |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2000113305A JP4162355B2 (en) | 2000-04-14 | 2000-04-14 | Hair dye composition |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2001294519A true JP2001294519A (en) | 2001-10-23 |
| JP4162355B2 JP4162355B2 (en) | 2008-10-08 |
Family
ID=18625294
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| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2000113305A Expired - Fee Related JP4162355B2 (en) | 2000-04-14 | 2000-04-14 | Hair dye composition |
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| Country | Link |
|---|---|
| JP (1) | JP4162355B2 (en) |
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| JP2011046614A (en) * | 2009-08-25 | 2011-03-10 | Hodogaya Chem Co Ltd | Alternate two-step type hair dye comprising basic dye and acidic dye and dyeing method therefor |
| US9289630B2 (en) | 2009-10-29 | 2016-03-22 | The Procter & Gamble Company | Hair conditioning composition comprising cationic surfactant system, direct dye, and nonionic thickener |
| WO2018115157A1 (en) * | 2016-12-22 | 2018-06-28 | L'oreal | Process for dyeing keratin fibres using at least one particular 2-azo(benz)imidazolium dye and at least one fluorescent dye |
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|---|---|
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