JP5328435B2 - Oxidative hair dye - Google Patents
Oxidative hair dye Download PDFInfo
- Publication number
- JP5328435B2 JP5328435B2 JP2009073046A JP2009073046A JP5328435B2 JP 5328435 B2 JP5328435 B2 JP 5328435B2 JP 2009073046 A JP2009073046 A JP 2009073046A JP 2009073046 A JP2009073046 A JP 2009073046A JP 5328435 B2 JP5328435 B2 JP 5328435B2
- Authority
- JP
- Japan
- Prior art keywords
- agent
- hair
- capsule
- hair dye
- oxidative hair
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Fee Related
Links
- 230000001590 oxidative effect Effects 0.000 title claims description 37
- 239000000118 hair dye Substances 0.000 title claims description 29
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 217
- 239000002775 capsule Substances 0.000 claims abstract description 39
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 claims abstract description 35
- 239000003513 alkali Substances 0.000 claims abstract description 18
- 239000007787 solid Substances 0.000 claims abstract description 7
- -1 metasilicate Chemical compound 0.000 claims description 49
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 17
- 239000007901 soft capsule Substances 0.000 claims description 12
- 239000007788 liquid Substances 0.000 claims description 9
- 229910019142 PO4 Inorganic materials 0.000 claims description 7
- 239000012528 membrane Substances 0.000 claims description 7
- 108010010803 Gelatin Proteins 0.000 claims description 6
- 239000008273 gelatin Substances 0.000 claims description 6
- 229920000159 gelatin Polymers 0.000 claims description 6
- 235000019322 gelatine Nutrition 0.000 claims description 6
- 235000011852 gelatine desserts Nutrition 0.000 claims description 6
- 229920001817 Agar Polymers 0.000 claims description 4
- 239000008272 agar Substances 0.000 claims description 4
- 229930195733 hydrocarbon Natural products 0.000 claims description 4
- 150000002430 hydrocarbons Chemical class 0.000 claims description 4
- BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical compound OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 claims description 3
- 239000004215 Carbon black (E152) Substances 0.000 claims description 3
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 claims description 3
- 235000011180 diphosphates Nutrition 0.000 claims description 3
- 239000010452 phosphate Substances 0.000 claims description 3
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 claims description 3
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- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 claims description 2
- KRKNYBCHXYNGOX-UHFFFAOYSA-K Citrate Chemical compound [O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O KRKNYBCHXYNGOX-UHFFFAOYSA-K 0.000 claims description 2
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 claims description 2
- 239000001177 diphosphate Substances 0.000 claims description 2
- XPPKVPWEQAFLFU-UHFFFAOYSA-J diphosphate(4-) Chemical compound [O-]P([O-])(=O)OP([O-])([O-])=O XPPKVPWEQAFLFU-UHFFFAOYSA-J 0.000 claims description 2
- 239000012530 fluid Substances 0.000 claims description 2
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- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 claims 1
- 239000000975 dye Substances 0.000 abstract description 35
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- 239000003051 hair bleaching agent Substances 0.000 description 18
- 238000011156 evaluation Methods 0.000 description 16
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- 230000000694 effects Effects 0.000 description 12
- 230000003647 oxidation Effects 0.000 description 12
- 238000007254 oxidation reaction Methods 0.000 description 12
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 11
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- KWIUHFFTVRNATP-UHFFFAOYSA-N glycine betaine Chemical compound C[N+](C)(C)CC([O-])=O KWIUHFFTVRNATP-UHFFFAOYSA-N 0.000 description 10
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- 238000007796 conventional method Methods 0.000 description 6
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- 235000021317 phosphate Nutrition 0.000 description 6
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 6
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- 239000002552 dosage form Substances 0.000 description 4
- 239000000499 gel Substances 0.000 description 4
- 229960002449 glycine Drugs 0.000 description 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 4
- 229920001296 polysiloxane Polymers 0.000 description 4
- 239000000843 powder Substances 0.000 description 4
- 239000008213 purified water Substances 0.000 description 4
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- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 3
- 206010040880 Skin irritation Diseases 0.000 description 3
- 229920002472 Starch Polymers 0.000 description 3
- 235000010419 agar Nutrition 0.000 description 3
- 150000001298 alcohols Chemical class 0.000 description 3
- 238000004042 decolorization Methods 0.000 description 3
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- 229940057995 liquid paraffin Drugs 0.000 description 3
- ZLNQQNXFFQJAID-UHFFFAOYSA-L magnesium carbonate Chemical compound [Mg+2].[O-]C([O-])=O ZLNQQNXFFQJAID-UHFFFAOYSA-L 0.000 description 3
- 239000001095 magnesium carbonate Substances 0.000 description 3
- 229910000021 magnesium carbonate Inorganic materials 0.000 description 3
- JXTPJDDICSTXJX-UHFFFAOYSA-N n-Triacontane Natural products CCCCCCCCCCCCCCCCCCCCCCCCCCCCCC JXTPJDDICSTXJX-UHFFFAOYSA-N 0.000 description 3
- 239000007800 oxidant agent Substances 0.000 description 3
- JRKICGRDRMAZLK-UHFFFAOYSA-L peroxydisulfate Chemical compound [O-]S(=O)(=O)OOS([O-])(=O)=O JRKICGRDRMAZLK-UHFFFAOYSA-L 0.000 description 3
- 239000000049 pigment Substances 0.000 description 3
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- YYGNTYWPHWGJRM-UHFFFAOYSA-N (6E,10E,14E,18E)-2,6,10,15,19,23-hexamethyltetracosa-2,6,10,14,18,22-hexaene Chemical compound CC(C)=CCCC(C)=CCCC(C)=CCCC=C(C)CCC=C(C)CCC=C(C)C YYGNTYWPHWGJRM-UHFFFAOYSA-N 0.000 description 2
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- KJCVRFUGPWSIIH-UHFFFAOYSA-N 1-naphthol Chemical compound C1=CC=C2C(O)=CC=CC2=C1 KJCVRFUGPWSIIH-UHFFFAOYSA-N 0.000 description 2
- WNWHHMBRJJOGFJ-UHFFFAOYSA-N 16-methylheptadecan-1-ol Chemical compound CC(C)CCCCCCCCCCCCCCCO WNWHHMBRJJOGFJ-UHFFFAOYSA-N 0.000 description 2
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- RNNHLXAEVKCLDG-UHFFFAOYSA-N 2,2,4,4,6,6,8,8-octamethyl-1,3,5,7,9,2,4,6,8,10-pentaoxapentasilecane Chemical compound C[Si]1(C)O[SiH2]O[Si](C)(C)O[Si](C)(C)O[Si](C)(C)O1 RNNHLXAEVKCLDG-UHFFFAOYSA-N 0.000 description 2
- JNAYPSWVMNJOPQ-UHFFFAOYSA-N 2,3-bis(16-methylheptadecanoyloxy)propyl 16-methylheptadecanoate Chemical compound CC(C)CCCCCCCCCCCCCCC(=O)OCC(OC(=O)CCCCCCCCCCCCCCC(C)C)COC(=O)CCCCCCCCCCCCCCC(C)C JNAYPSWVMNJOPQ-UHFFFAOYSA-N 0.000 description 2
- GECRRQVLQHRVNH-MRCUWXFGSA-N 2-octyldodecyl (z)-octadec-9-enoate Chemical compound CCCCCCCCCCC(CCCCCCCC)COC(=O)CCCCCCC\C=C/CCCCCCCC GECRRQVLQHRVNH-MRCUWXFGSA-N 0.000 description 2
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 2
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- ATRRKUHOCOJYRX-UHFFFAOYSA-N Ammonium bicarbonate Chemical compound [NH4+].OC([O-])=O ATRRKUHOCOJYRX-UHFFFAOYSA-N 0.000 description 2
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- XMSXQFUHVRWGNA-UHFFFAOYSA-N Decamethylcyclopentasiloxane Chemical compound C[Si]1(C)O[Si](C)(C)O[Si](C)(C)O[Si](C)(C)O[Si](C)(C)O1 XMSXQFUHVRWGNA-UHFFFAOYSA-N 0.000 description 2
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- VBIIFPGSPJYLRR-UHFFFAOYSA-M Stearyltrimethylammonium chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCCCC[N+](C)(C)C VBIIFPGSPJYLRR-UHFFFAOYSA-M 0.000 description 2
- BHEOSNUKNHRBNM-UHFFFAOYSA-N Tetramethylsqualene Natural products CC(=C)C(C)CCC(=C)C(C)CCC(C)=CCCC=C(C)CCC(C)C(=C)CCC(C)C(C)=C BHEOSNUKNHRBNM-UHFFFAOYSA-N 0.000 description 2
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- 235000019818 tetrasodium diphosphate Nutrition 0.000 description 1
- 239000001577 tetrasodium phosphonato phosphate Substances 0.000 description 1
- VLPFTAMPNXLGLX-UHFFFAOYSA-N trioctanoin Chemical compound CCCCCCCC(=O)OCC(OC(=O)CCCCCCC)COC(=O)CCCCCCC VLPFTAMPNXLGLX-UHFFFAOYSA-N 0.000 description 1
- 235000015870 tripotassium citrate Nutrition 0.000 description 1
- 229910000404 tripotassium phosphate Inorganic materials 0.000 description 1
- 235000019798 tripotassium phosphate Nutrition 0.000 description 1
- RYFMWSXOAZQYPI-UHFFFAOYSA-K trisodium phosphate Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])([O-])=O RYFMWSXOAZQYPI-UHFFFAOYSA-K 0.000 description 1
- 229910000406 trisodium phosphate Inorganic materials 0.000 description 1
- 235000019801 trisodium phosphate Nutrition 0.000 description 1
- XPFJYKARVSSRHE-UHFFFAOYSA-K trisodium;2-hydroxypropane-1,2,3-tricarboxylate;2-hydroxypropane-1,2,3-tricarboxylic acid Chemical class [Na+].[Na+].[Na+].OC(=O)CC(O)(C(O)=O)CC(O)=O.[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O XPFJYKARVSSRHE-UHFFFAOYSA-K 0.000 description 1
- 229960004418 trolamine Drugs 0.000 description 1
- 238000001771 vacuum deposition Methods 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- UHVMMEOXYDMDKI-JKYCWFKZSA-L zinc;1-(5-cyanopyridin-2-yl)-3-[(1s,2s)-2-(6-fluoro-2-hydroxy-3-propanoylphenyl)cyclopropyl]urea;diacetate Chemical compound [Zn+2].CC([O-])=O.CC([O-])=O.CCC(=O)C1=CC=C(F)C([C@H]2[C@H](C2)NC(=O)NC=2N=CC(=CC=2)C#N)=C1O UHVMMEOXYDMDKI-JKYCWFKZSA-L 0.000 description 1
Landscapes
- Cosmetics (AREA)
Abstract
Description
本発明は、毛髪処理剤に関する。詳しくは、カプセル化された第1剤と、過酸化水素を含有する第2剤とからなる、毛髪脱色剤や酸化染毛剤などに用いる毛髪処理剤に関する。尚、本発明における室温とは、1〜30℃の雰囲気下の温度範囲をいう。 The present invention relates to a hair treatment agent. Specifically, the present invention relates to a hair treatment agent used for a hair bleaching agent, an oxidative hair dye, or the like, comprising a first encapsulated agent and a second agent containing hydrogen peroxide. In addition, the room temperature in this invention means the temperature range under 1-30 degreeC atmosphere.
一般に、毛髪脱色剤や酸化染毛剤などの毛髪処理剤は、アルカリ剤を含有する第1剤と、過酸化水素を含有する第2剤とからなる二剤式のものが主流である。ニ剤式の毛髪脱色剤は、使用時に第1剤と第2剤とを混合し、毛髪中のメラニン色素を酸化分解することにより毛髪を脱色する。また、第1剤に更に酸化染料を配合した酸化染毛剤は、メラニン色素を酸化分解すると共に、酸化染料を毛髪内で酸化重合して毛髪を所望の色に染色する。 In general, hair treatment agents such as hair bleaching agents and oxidative hair dyes are mainly of a two-component type comprising a first agent containing an alkaline agent and a second agent containing hydrogen peroxide. The two-component hair bleaching agent mixes the first agent and the second agent at the time of use, and decolorizes the hair by oxidizing and decomposing melanin pigment in the hair. Moreover, the oxidative hair dye which mix | blended the oxidative dye with the 1st agent oxidizes and decomposes | disassembles a melanin pigment, and oxidatively polymerizes an oxidative dye in hair and dye | stains hair to a desired color.
したがって、より毛髪を脱色したい場合、或いは明るい色に染毛したい場合には、メラニン色素を十分に分解するために過酸化水素の配合量を増大させることが必要となる。 Therefore, when it is desired to decolorize the hair or to dye the hair to a lighter color, it is necessary to increase the amount of hydrogen peroxide in order to sufficiently decompose the melanin pigment.
しかし、第2剤に配合する過酸化水素の量は、日本においては、薬事法により上限6質量%に規制されている。また、欧州諸国においても、EU化粧品指令 AnnexIIIにより上限12質量%に規制されている。したがって、過酸化水素の配合量を規制量以上に配合できないという問題がある。 However, the amount of hydrogen peroxide to be blended in the second agent is restricted to an upper limit of 6 mass% by the Pharmaceutical Affairs Law in Japan. Also in European countries, the upper limit is 12 mass% by the EU cosmetics directive Annex III. Therefore, there exists a problem that the compounding quantity of hydrogen peroxide cannot be mix | blended more than regulation amount.
このような問題を解決し、毛髪をより脱色するために、過硫酸塩などの促進剤を第1剤に配合、或いは、第3剤として用いる毛髪脱色剤が知られている(例えば、特許文献1〜3を参照)。 In order to solve such problems and to further decolorize hair, a hair decoloring agent is known which contains an accelerator such as persulfate in the first agent or is used as the third agent (for example, Patent Documents). 1-3).
しかし、このような強い酸化力を有する過硫酸塩などを酸化染毛剤に用いると、酸化染料が毛髪内に浸透する前に酸化されたり、酸化された染料の重合体が分解したりして、毛髪を十分に染毛することができないという問題がある。また、このような第1剤や第3剤は、通常、粉末状の剤型で用いられることから、第2剤との混合時に、粉体が舞い散るという問題もある。 However, if such a persulfate having a strong oxidizing power is used as an oxidative hair dye, the oxidative dye may be oxidized before penetrating into the hair, or the polymer of the oxidized dye may be decomposed. There is a problem that the hair cannot be dyed sufficiently. Moreover, since such a 1st agent and a 3rd agent are normally used with a powdery dosage form, there also exists a problem that powder will disperse at the time of mixing with a 2nd agent.
本発明は、前記従来技術に鑑みなされたものであって、第1剤と第2剤の混合時に、第1剤が舞い散ることがなく、容易に混合することができ、しかも、過酸化水素の規制された量であっても、より毛髪を脱色できる毛髪処理剤を提供することを課題とする。また、酸化染毛剤の態様で用いた場合には、酸化染料の保存安定性に優れ、しかも、過酸化水素の規制された量であっても、毛髪を明るい色調にも染毛できる毛髪処理剤を提供することを課題とする。 The present invention has been made in view of the above-described prior art, and when the first agent and the second agent are mixed, the first agent is not scattered and can be easily mixed. It is an object of the present invention to provide a hair treatment agent that can decolorize hair even if the amount is regulated. In addition, when used in the form of an oxidative hair dye, a hair treatment that is excellent in the storage stability of oxidative dyes and that can dye hair in a light color tone even with a regulated amount of hydrogen peroxide. It is an object to provide an agent.
すなわち、本発明は、
〔1〕 アルカリ剤を内包したカプセルからなる第1剤と、過酸化水素を含有する第2剤とからなる毛髪処理剤、
〔2〕 更に、油性成分をカプセルに内包してなる前記〔1〕に記載の毛髪処理剤、
〔3〕 油性成分が、室温で液状の油性成分である前記〔2〕に記載の毛髪処理剤、
〔4〕 室温で液状の油性成分が、炭化水素油及び/又はシリコーン油である前記〔3〕に記載の毛髪処理剤、
〔5〕 アルカリ剤が、固体のアルカリ剤である前記〔1〕〜〔4〕のいずれかに記載の毛髪処理剤、
〔6〕 固体のアルカリ剤が、炭酸塩、炭酸水素塩、酒石酸塩、クエン酸塩、リン酸塩、二リン酸塩、ケイ酸塩、メタケイ酸塩、酢酸塩からなる群から選ばれる1種以上である前記〔5〕に記載の毛髪処理剤、
〔7〕 カプセルの壁膜体が、ゼラチン及び/又は寒天である前記〔1〕〜〔6〕のいずれかに記載の毛髪処理剤、
〔8〕 カプセルに内包される成分に、実質的に水を含有しないことを特徴とする前記〔〔1〕〜〔7〕のいずれかに記載の毛髪処理剤、
〔9〕 カプセルが、ソフトカプセルであることを特徴とする前記〔1〕〜〔8〕のいずれかに記載の毛髪処理剤、並びに
〔10〕 第2剤が、流動性を有する第2剤であることを特徴とする前記〔1〕〜〔9〕のいずれかに記載の毛髪処理剤
に関する。
That is, the present invention
[1] A hair treatment agent comprising a first agent comprising a capsule containing an alkali agent and a second agent comprising hydrogen peroxide,
[2] The hair treatment agent according to [1], further comprising an oil component encapsulated in a capsule,
[3] The hair treatment agent according to [2], wherein the oily component is a liquid oily component at room temperature,
[4] The hair treatment agent according to [3], wherein the oily component that is liquid at room temperature is a hydrocarbon oil and / or a silicone oil,
[5] The hair treatment agent according to any one of [1] to [4], wherein the alkaline agent is a solid alkaline agent,
[6] The solid alkaline agent is one selected from the group consisting of carbonates, bicarbonates, tartrate, citrate, phosphate, diphosphate, silicate, metasilicate, and acetate. The hair treatment agent according to [5] above,
[7] The hair treatment agent according to any one of [1] to [6], wherein the capsule wall membrane is gelatin and / or agar,
[8] The hair treatment agent according to any one of the above [[1] to [7], wherein the component contained in the capsule does not substantially contain water,
[9] The hair treatment agent according to any one of [1] to [8], wherein the capsule is a soft capsule, and [10] the second agent is a second agent having fluidity. The hair treatment agent according to any one of the above [1] to [9].
本発明の毛髪処理剤は、第1剤と第2剤の混合時に、第1剤が舞い散ることがなく、容易に混合することができ、しかも、過酸化水素の規制された量であっても、より毛髪を脱色できるという効果を奏する。また、本発明の毛髪処理剤を酸化染毛剤の態様で用いると、酸化染料の保存安定性に優れ、しかも、過酸化水素の規制された量であっても、毛髪を明るい色調にも染毛できるという効果を奏する。 The hair treatment agent of the present invention can be easily mixed without mixing the first agent when the first agent and the second agent are mixed, and has a regulated amount of hydrogen peroxide. Also has the effect of being able to decolorize the hair more. Further, when the hair treatment agent of the present invention is used in the form of an oxidative hair dye, the oxidative dye is excellent in storage stability, and even if the amount of hydrogen peroxide is regulated, the hair is dyed in a light color tone. It has the effect of being able to hair.
本発明の毛髪処理剤は、アルカリ剤を内包したカプセルからなる第1剤と、過酸化水素を含有する第2剤とから構成される。まず、本発明の第1剤について説明する。 The hair treatment agent of this invention is comprised from the 1st agent which consists of a capsule which included the alkaline agent, and the 2nd agent containing hydrogen peroxide. First, the 1st agent of this invention is demonstrated.
本発明に用いるアルカリ剤は、本発明の効果を発揮すれば特に限定されず、無機アルカリ剤及び有機アルカリ剤を用いることができる。無機アルカリ剤としては、例えば、炭酸ナトリウム、炭酸カリウム、炭酸アンモニウム等の炭酸塩;炭酸水素ナトリウム、炭酸水素カリウム、炭酸水素アンモニウム等の炭酸水素塩;酒石酸カリウムナトリウムなどの酒石酸塩;クエン酸三ナトリウム、クエン酸三カリウムなどのクエン酸塩;リン酸三ナトリウム、リン酸三カリウムなどのリン酸塩;ピロリン酸ナトリウムなどのピロリン酸塩;ケイ酸ナトリウムなどのケイ酸塩;メタケイ酸ナトリウムなどのメタケイ酸塩;酢酸ナトリウム、酢酸カリウム、酢酸カルシウムなどの酢酸塩等を例示することができる。また、有機アルカリ剤としては、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、イソプロパノールアミン、2−アミノ−2−メチル−1−プロパノール、2−アミノ−2−メチル−1,3−プロパンジオール等を例示することができる。なかでも、pH上昇効果の観点から、炭酸塩、炭酸水素塩、リン酸塩、ケイ酸塩等の固体のアルカリ剤を用いるのが好ましく、第2剤中での分散性の観点から、粉末状にして用いるのがより好ましい。尚、これらのアルカリ剤は、1種を単独で用いても良く、2種以上を適宜混合して用いても良い。 The alkali agent used for this invention will not be specifically limited if the effect of this invention is exhibited, An inorganic alkali agent and an organic alkali agent can be used. Examples of the inorganic alkaline agent include carbonates such as sodium carbonate, potassium carbonate and ammonium carbonate; hydrogen carbonates such as sodium hydrogen carbonate, potassium hydrogen carbonate and ammonium hydrogen carbonate; tartrate salts such as potassium sodium tartrate; trisodium citrate Citrates such as tripotassium citrate; phosphates such as trisodium phosphate and tripotassium phosphate; pyrophosphates such as sodium pyrophosphate; silicates such as sodium silicate; metasilicates such as sodium metasilicate Acid salts; acetates such as sodium acetate, potassium acetate and calcium acetate can be exemplified. Examples of the organic alkali agent include monoethanolamine, diethanolamine, triethanolamine, isopropanolamine, 2-amino-2-methyl-1-propanol, 2-amino-2-methyl-1,3-propanediol, etc. can do. Among these, it is preferable to use a solid alkali agent such as carbonate, hydrogen carbonate, phosphate, silicate, etc. from the viewpoint of the effect of raising the pH, and from the viewpoint of dispersibility in the second agent, it is powdery. More preferably, it is used. In addition, these alkali agents may be used individually by 1 type, and may mix and use 2 or more types suitably.
アルカリ剤の毛髪処理剤中の含有量は、本発明の効果を発揮すれば特に限定されないが、毛髪の脱色力の観点から、第2剤と混合した際に1質量%以上となる量を用いることが好ましく、より好ましくは、3質量%以上となる量である。また、安全性や皮膚刺激の観点から、第2剤と混合した際に20質量%以下となる量を用いることが好ましく、より好ましくは、15質量%以下となる量である。これらのことから、アルカリ剤の毛髪処理剤中での含有量は、好ましくは1〜20質量%であり、より好ましくは3〜15質量%である。 The content of the alkaline agent in the hair treatment agent is not particularly limited as long as the effect of the present invention is exhibited, but from the viewpoint of the depigmenting power of the hair, an amount that is 1% by mass or more when mixed with the second agent is used. The amount is preferably 3% by mass or more. In addition, from the viewpoint of safety and skin irritation, it is preferable to use an amount that is 20% by mass or less, more preferably 15% by mass or less when mixed with the second agent. From these things, content in the hair treatment agent of an alkaline agent becomes like this. Preferably it is 1-20 mass%, More preferably, it is 3-15 mass%.
本発明の毛髪処理剤は、毛髪脱色剤として用いる場合は、上記の如く、アルカリ剤が必須の成分として第1剤を構成するが、酸化染毛剤として用いる場合は、第1剤のカプセル中に、更に酸化染料が配合される。 When the hair treatment agent of the present invention is used as a hair bleaching agent, as described above, the alkaline agent constitutes the first agent as an essential component, but when used as an oxidative hair dye, in the capsule of the first agent. Further, an oxidation dye is blended.
本発明における酸化染料とは、自身の酸化重合により発色する染料前駆体、および染料前駆体との反応により種々の色相とするカップラーの双方を意味する。本発明に用いることのできる酸化染料前駆体としては、例えば、フェニレンジアミン類、アミノフェノール類、ジアミノピリジン類、及びそれらの塩酸塩、硫酸塩等の塩類等が挙げられる。具体的には、p−フェニレンジアミン、トルエン−2,5−ジアミン、トルエン−3,4−ジアミン、2,5−ジアミノアニソール、N−フェニル−p−フェニレンジアミン、N−メチル−p−フェニレンジアミン、N,N−ジメチル−p−フェニレンジアミン、6−メトキシ−3−メチル−p−フェニレンジアミン、N,N−ジエチル−2−メチル−p−フェニレンジアミン、N−エチル−N−(ヒドロキシエチル)−p−フェニレンジアミン、N−(2−ヒドロキシプロピル)−p−フェニレンジアミン、2−クロル−6−メチル−p−フェニレンジアミン、2−クロロ−p−フェニレンジアミン、N,N−ビス−(2−ヒドロキシエチル)−p−フェニレンジアミン、2,6−ジクロル−p−フェニレンジアミン、2−クロル−6−ブロム−p−フェニレンジアミン等のフェニレンジアミン類;パラアミノフェノール、オルトアミノフェノール、パラメチルアミノフェノール、2,4−ジアミノフェノール、5−アミノサリチル酸、2−メチル−4−アミノフェノール、3−メチル−4−アミノフェノール、2,6−ジメチル−4−アミノフェノール、3,5−ジメチル−4−アミノフェノール、2,3−ジメチル−4−アミノフェノール、2,5−ジメチル−4−アミノフェノール、2−クロロ−4−アミノフェノール、3−クロロ−4−アミノフェノール等のアミノフェノール類;2,5−ジアミノピリジン等のジアミノピリジン類等及びそれらの塩類等を例示することができる。 The oxidative dye in the present invention means both a dye precursor that develops color by its own oxidative polymerization and a coupler that has various hues by reaction with the dye precursor. Examples of the oxidative dye precursor that can be used in the present invention include phenylenediamines, aminophenols, diaminopyridines, and salts thereof such as hydrochlorides and sulfates. Specifically, p-phenylenediamine, toluene-2,5-diamine, toluene-3,4-diamine, 2,5-diaminoanisole, N-phenyl-p-phenylenediamine, N-methyl-p-phenylenediamine N, N-dimethyl-p-phenylenediamine, 6-methoxy-3-methyl-p-phenylenediamine, N, N-diethyl-2-methyl-p-phenylenediamine, N-ethyl-N- (hydroxyethyl) -P-phenylenediamine, N- (2-hydroxypropyl) -p-phenylenediamine, 2-chloro-6-methyl-p-phenylenediamine, 2-chloro-p-phenylenediamine, N, N-bis- (2 -Hydroxyethyl) -p-phenylenediamine, 2,6-dichloro-p-phenylenediamine, 2-chloro-6-butyl Phenylenediamines such as mu-p-phenylenediamine; paraaminophenol, orthoaminophenol, paramethylaminophenol, 2,4-diaminophenol, 5-aminosalicylic acid, 2-methyl-4-aminophenol, 3-methyl-4 -Aminophenol, 2,6-dimethyl-4-aminophenol, 3,5-dimethyl-4-aminophenol, 2,3-dimethyl-4-aminophenol, 2,5-dimethyl-4-aminophenol, 2- Examples thereof include aminophenols such as chloro-4-aminophenol and 3-chloro-4-aminophenol; diaminopyridines such as 2,5-diaminopyridine, and salts thereof.
カップラーとしては、例えば、レゾルシン、m−アミノフェノール、m−フェニレンジアミン、2,4−ジアミノフェノキシエタノール、5−アミノ−o−クレゾール、2−メチル−5−ヒドロキシエチルアミノフェノール、2,6−ジアミノピリジン、カテコール、ピロガロール、α−ナフトール、没食子酸、タンニン酸等及びそれらの塩類等を例示することができる。 Examples of the coupler include resorcin, m-aminophenol, m-phenylenediamine, 2,4-diaminophenoxyethanol, 5-amino-o-cresol, 2-methyl-5-hydroxyethylaminophenol, and 2,6-diaminopyridine. , Catechol, pyrogallol, α-naphthol, gallic acid, tannic acid and the like and salts thereof.
本発明では、これら酸化染料のうち、固体粉末状のアルカリ剤と伴に用いる場合、混合性の観点から、固体の酸化染料を用いるのが好ましく、第2剤中での分散性の観点から粉末状にして用いるのがより好ましい。 In the present invention, among these oxidation dyes, when used together with a solid powdery alkaline agent, it is preferable to use a solid oxidation dye from the viewpoint of mixing properties, and from the viewpoint of dispersibility in the second agent, More preferably, it is used in the form.
酸化染料の毛髪処理剤中の含有量は、本発明の効果を発揮すれば特に限定されないが、毛髪への染色性の観点から、第2剤と混合した際に0.1質量%以上となる量を用いることが好ましく、0.2質量%以上となる量がより好ましい。また、皮膚刺激の観点から、第2剤と混合した際に2質量%以下となる量を用いることが好ましく、1.5質量%以下となる量がより好ましい。これらのことから、酸化染料の毛髪処理剤中での含有量は、好ましくは0.1〜2質量%であり、より好ましくは0.2〜1.5質量%である。 The content of the oxidative dye in the hair treatment agent is not particularly limited as long as the effect of the present invention is exhibited. However, from the viewpoint of dyeability to hair, the content becomes 0.1% by mass or more when mixed with the second agent. The amount is preferably used, and more preferably 0.2% by mass or more. From the viewpoint of skin irritation, it is preferable to use an amount that is 2% by mass or less when mixed with the second agent, and an amount that is 1.5% by mass or less is more preferable. From these things, content in the hair treatment agent of an oxidation dye becomes like this. Preferably it is 0.1-2 mass%, More preferably, it is 0.2-1.5 mass%.
本発明の第1剤のカプセル中には、更に油性成分を内包させることができ、この油性成分に、前記アルカリ剤或いは、アルカリ剤と酸化染料を分散させるのが好ましい。これにより、第2剤との混合時に、アルカリ剤或いは、アルカリ剤と酸化染料の分散性がより良好となるという利点がある。 In the capsule of the first agent of the present invention, an oily component can be further encapsulated, and it is preferable to disperse the alkali agent or the alkali agent and an oxidation dye in the oily component. Thereby, there exists an advantage that the dispersibility of an alkali agent or an alkali agent and an oxidation dye becomes more favorable at the time of mixing with a 2nd agent.
用い得る油性成分は、アルカリ剤の分散媒として用いることができれば特に限定されないが、例えば、オリーブ油、ツバキ油、マカデミアナッツ油、アボカド油等の油脂;カルナバロウ、キャンデリラロウ、ホホバ油、ミツロウ、ラノリン等のロウ類;流動パラフィン、パラフィン、ワセリン、セレシン、マイクロクリスタリンワックス、スクワレン、スクワラン等の炭化水素;メチルポリシロキサン、メチルフェニルポリシロキサン、メチルシクロポリシロキサン、オクタメチルシクロテトラシロキサン、オクタメチルシクロペンタシロキサン、デカメチルシクロペンタシロキサン、メチルハイドロジェンポリシロキサン、アミノエチルアミノプロピルメチルシロキサン・ジメチルシロキサン共重合体、高重合メチルポリシロキサン、ポリオキシエチレン・メチルポリシロキサン共重合体等のシリコーン類;ミリスチン酸イソプロピル、ミリスチン酸2−オクチルドデシル、2−エチルヘキサン酸セチル、パルミチン酸2−エチルヘキシル、ジ−2−エチルヘキサン酸ネオペンチルグリコール、トリ−2−エチルヘキサン酸グリセロール、オレイン酸2−オクチルドデシル、トリイソステアリン酸グリセロール、トリ−2−エチルヘキサン酸グリセロール、オレイン酸2−オクチルドデシル、リンゴ酸ジイソステアリル、トリイソステアリン酸グリセロール、2−エチルヘキサン酸ジグリセリド等の脂肪酸エステル;トリカプリル酸グリセリル、トリ2−エチルヘキサン酸グリセリル、トリウンデシル酸グリセリル、トリステアリン酸グリセリル等の脂肪酸トリグリセリドエステル;セチルアルコール、ステアリルアルコール、イソステアリルアルコール、2−オクチルドデカノール、オレイルアルコール等の高級アルコール類;ラウリン酸、ミリスチン酸、パルミチン酸、ステアリン酸、イソステアリン酸、オレイン酸等の高級脂肪酸などが挙げられる。 The oily component that can be used is not particularly limited as long as it can be used as a dispersion medium for an alkaline agent. For example, oils and fats such as olive oil, camellia oil, macadamia nut oil, and avocado oil; Waxes such as liquid paraffin, paraffin, petrolatum, ceresin, microcrystalline wax, squalene, squalane, etc .; methylpolysiloxane, methylphenylpolysiloxane, methylcyclopolysiloxane, octamethylcyclotetrasiloxane, octamethylcyclopentasiloxane , Decamethylcyclopentasiloxane, methylhydrogenpolysiloxane, aminoethylaminopropylmethylsiloxane / dimethylsiloxane copolymer, highly polymerized methylpolysiloxane, poly Silicones such as xylene / methylpolysiloxane copolymer; isopropyl myristate, 2-octyldodecyl myristate, cetyl 2-ethylhexanoate, 2-ethylhexyl palmitate, dipentyl glycol di-2-ethylhexanoate, tri- Glycerol 2-ethylhexanoate, 2-octyldodecyl oleate, glycerol triisostearate, glycerol tri-2-ethylhexanoate, 2-octyldodecyl oleate, diisostearyl malate, glycerol triisostearate, 2-ethylhexane Fatty acid esters such as acid diglycerides; fatty acid triglyceride esters such as glyceryl tricaprylate, glyceryl tri-2-ethylhexanoate, glyceryl triundecylate, and glyceryl tristearate Higher alcohols such as cetyl alcohol, stearyl alcohol, isostearyl alcohol, 2-octyldodecanol and oleyl alcohol; higher fatty acids such as lauric acid, myristic acid, palmitic acid, stearic acid, isostearic acid and oleic acid .
なかでも、アルカリ剤の分散性の観点から、室温で液状の油性成分を用いるのが好ましく、安定性の観点から流動パラフィン、スクワレン、スクワラン等の炭化水素油;メチルポリシロキサン、メチルフェニルポリシロキサン、メチルシクロポリシロキサン、オクタメチルシクロテトラシロキサン、オクタメチルシクロペンタシロキサン、デカメチルシクロペンタシロキサン、メチルハイドロジェンポリシロキサン等のシリコーン油などを用いるのがより好ましい。尚、これらの油性成分は、1種を単独で用いても良く、2種以上を適宜混合して用いても良い。 Among these, from the viewpoint of dispersibility of the alkaline agent, it is preferable to use an oily component that is liquid at room temperature. From the viewpoint of stability, hydrocarbon oils such as liquid paraffin, squalene, and squalane; methylpolysiloxane, methylphenylpolysiloxane, It is more preferable to use silicone oils such as methylcyclopolysiloxane, octamethylcyclotetrasiloxane, octamethylcyclopentasiloxane, decamethylcyclopentasiloxane, methylhydrogenpolysiloxane, and the like. In addition, these oily components may be used individually by 1 type, and may mix and use 2 or more types suitably.
本発明の毛髪処理剤を毛髪脱色剤として用いる場合、第1剤のカプセル中の油性成分の含有量は、本発明の効果を発揮すれば特に限定されないが、アルカリ剤の分散性の観点から、アルカリ剤の0.5質量倍以上が好ましく、0.8質量倍以上がより好ましい。また、毛髪への残留性及び洗浄性の観点から、アルカリ剤の10質量倍以下が好ましく、5質量倍以下がより好ましい。これらのことから、カプセル中における油性成分の含有量は、好ましくはアルカリ剤の0.5〜10質量倍であり、より好ましくは0.8〜5質量倍である。 When the hair treatment agent of the present invention is used as a hair bleaching agent, the content of the oil component in the capsule of the first agent is not particularly limited as long as the effect of the present invention is exhibited, but from the viewpoint of dispersibility of the alkaline agent, 0.5 mass times or more of the alkali agent is preferable, and 0.8 mass times or more is more preferable. Moreover, 10 mass times or less of an alkaline agent is preferable from a viewpoint of the persistence to hair and a washability, and 5 mass times or less are more preferable. From these things, content of the oil-based component in a capsule becomes like this. Preferably it is 0.5-10 mass times of an alkaline agent, More preferably, it is 0.8-5 mass times.
本発明の毛髪処理剤を酸化染毛剤として用いる場合、第1剤のカプセル中の油性成分の含有量は、本発明の効果を発揮すれば特に限定されないが、アルカリ剤及び酸化染料の分散性の観点から、アルカリ剤と酸化染料の合計量の0.5質量倍以上が好ましく、0.8質量倍以上がより好ましい。また、毛髪への残留性及び洗浄性の観点から、アルカリ剤と酸化染料の合計量の10質量倍以下が好ましく、5質量倍以下がより好ましい。これらのことから、カプセル中における油性成分の含有量は、好ましくはアルカリ剤と酸化染料の合計量の0.5〜10質量倍であり、より好ましくは0.8〜5質量倍である。 When the hair treatment agent of the present invention is used as an oxidative hair dye, the content of the oil component in the capsule of the first agent is not particularly limited as long as the effect of the present invention is exhibited, but the dispersibility of the alkali agent and the oxidative dye In view of the above, 0.5 mass times or more of the total amount of the alkali agent and the oxidation dye is preferable, and 0.8 mass times or more is more preferable. Further, from the viewpoints of persistence to hair and detergency, it is preferably 10 times by mass or less and more preferably 5 times by mass or less of the total amount of the alkaline agent and the oxidation dye. From these things, content of the oil-based component in a capsule becomes like this. Preferably it is 0.5-10 mass times of the total amount of an alkaline agent and an oxidation dye, More preferably, it is 0.8-5 mass times.
本発明に係る第1剤には、本発明の目的の効果を損なわない範囲であれば、上記した成分のほか、ソルビタン脂肪酸エステル、グリセリン脂肪酸エステル、及びこれらのアルキレンオキシド付加物、ポリグリセリン脂肪酸エステル、ポリオキシアルキレンアルキルエーテル、ポリオキシアルキレン脂肪酸エステル、ポリオキシエチレン硬化ヒマシ油、ポリオキシエチレンラノリン、ポリオキシエチレン還元ラノリン等のノニオン性界面活性剤;高級脂肪酸石鹸、アルキル硫酸エステル塩、アルキルリン酸塩、ポリオキシエチレンアルキルエーテル硫酸塩、アルキルエーテルリン酸エステル、アルキルエーテルカルボン酸塩、アシルメチルタウリン塩、アルキルスルホコハク酸及びその塩等のアニオン性界面活性剤;アルキルグリシン塩、カルボキシメチルグリシン塩、N−アシルアミノエチル−N−2−ヒドロキシエチルグリシン塩等のグリシン型両性界面活性剤、アルキルアミノプロピオン酸塩、アルキルイミノジプロピオン酸塩等のアミノプロピオン酸型両性界面活性剤、アルキルジメチルアミノ酢酸ベタイン、脂肪酸アミドプロピルジメチルアミノ酢酸ベタイン等のアミノ酢酸ベタイン型両性界面活性剤、アルキルヒドロキシスルホベタイン等のスルホベタイン型両性界面活性剤等の両性界面活性剤;塩化ラウリ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、塩化ジステアリルジメチルアンモニウムなどのアルキルアミン塩;ミリスチン酸ジメチルアミノエチルアミド、ステアリン酸ジエチルアミノプロピルアミドなどの脂肪酸アミドアミン等のカチオン性界面活性剤;アスコルビ酸、エリソルビン酸等の酸化防止剤、増粘剤、キレート剤、色素、分散剤等を適宜配合することができる。 In the first agent according to the present invention, as long as the effects of the object of the present invention are not impaired, sorbitan fatty acid ester, glycerin fatty acid ester, and alkylene oxide adducts thereof, polyglycerin fatty acid ester, in addition to the above-described components Nonionic surfactants such as polyoxyalkylene alkyl ether, polyoxyalkylene fatty acid ester, polyoxyethylene hydrogenated castor oil, polyoxyethylene lanolin, polyoxyethylene reduced lanolin; higher fatty acid soap, alkyl sulfate ester salt, alkyl phosphoric acid Anionic surfactants such as salts, polyoxyethylene alkyl ether sulfates, alkyl ether phosphates, alkyl ether carboxylates, acylmethyl taurates, alkylsulfosuccinic acids and salts thereof; alkyl glycine salts, cals Glycine-type amphoteric surfactants such as xymethylglycine salt and N-acylaminoethyl-N-2-hydroxyethylglycine salt, and aminopropionic acid-type amphoteric surfactants such as alkylaminopropionate and alkyliminodipropionate Amphoteric surfactants such as aminoacetic acid betaine-type amphoteric surfactants such as alkyldimethylaminoacetic acid betaine and fatty acid amidopropyldimethylaminoacetic acid betaine; and sulfobetaine-type amphoteric surfactants such as alkylhydroxysulfobetaine; lauryltrimethylammonium chloride; Alkylamine salts such as stearyltrimethylammonium chloride and distearyldimethylammonium chloride; cuts of fatty acid amidoamines such as myristic acid dimethylaminoethylamide and stearic acid diethylaminopropylamide Emissions surfactant; ascorbic acid, antioxidants such as erythorbic acid, thickeners, chelating agents, dyes, can be appropriately blended dispersant.
かくして、前記第1剤の内容物を内包するカプセルとしては、後述する第2剤に投入できれば特に限定されないが、ソフトカプセルやハードカプセルなどのミニカプセルや、マイクロカプセル、ナノカプセル等を挙げることができる。 Thus, the capsule containing the contents of the first agent is not particularly limited as long as it can be introduced into the second agent described later, and examples thereof include mini capsules such as soft capsules and hard capsules, microcapsules, and nanocapsules.
カプセルの製法は、特に限定されず、既知の方法でカプセル化することができる。例えば、マイクロカプセル化やナノカプセル化するのであれば、界面重縮合法、コアセルベーション法、界面沈殿法、真空蒸着皮膜法、スプレードライ法等を挙げることができる。ソフトカプセル化するのであれば、打ち抜き法や滴下法等を挙げることができ、ハードカプセル化するのであれば、浸漬法等を上げることができる。 The manufacturing method of a capsule is not specifically limited, It can encapsulate by a known method. For example, in the case of microencapsulation or nanoencapsulation, an interfacial polycondensation method, a coacervation method, an interfacial precipitation method, a vacuum deposition film method, a spray drying method, and the like can be given. In the case of soft encapsulation, a punching method, a dropping method, or the like can be given, and in the case of hard encapsulation, an immersion method or the like can be raised.
尚、粉末状の成分或いは粉末を分散させた液状成分を容易にカプセル化できることから、ミニカプセル化するのが好ましく、水性媒体中での崩壊性の観点から、ソフトカプセル化するのがより好ましい。また、ソフトカプセル化する場合、球状のカプセルのみならず、三角型、ひし型、魚型、ボトル型等の種々の形状のカプセルが得られることから、打ち抜き法により製造するのが好ましい。種々の形状のカプセルとすることで、使用者に毛髪処理剤の使用時の楽しさを提供することができるという利点がある。 In addition, since the powdery component or the liquid component in which the powder is dispersed can be easily encapsulated, mini-encapsulation is preferable, and from the viewpoint of disintegration in an aqueous medium, soft encapsulation is more preferable. When soft capsules are produced, not only spherical capsules but also capsules of various shapes such as triangles, diamonds, fishes, bottles and the like are obtained. By making capsules of various shapes, there is an advantage that it is possible to provide the user with fun when using the hair treatment agent.
また、ソフトカプセル化した場合、カプセルの第2剤中での分散性並びに崩壊性の観点から、直径が0.1mm〜30mm程度のカプセルとするのが好ましく、直径が0.5mm〜25mm程度のとするのがより好ましい。 In addition, in the case of soft encapsulation, from the viewpoint of dispersibility and disintegration of the capsule in the second agent, the capsule preferably has a diameter of about 0.1 mm to 30 mm, and the diameter is about 0.5 mm to 25 mm. More preferably.
壁膜体の膜厚は、カプセルの強度並びに第2剤中での崩壊性の観点から、50μm〜500μm程度とするのが好ましい。 The film thickness of the wall membrane is preferably about 50 to 500 μm from the viewpoint of capsule strength and disintegration in the second agent.
前記第1剤の内容物を内包物質としてソフトカプセル化する場合、カプセルの壁膜体はカプセル化できれば特に限定されないが、ゼラチン、カンテン、カラギーナン、デンプン等を例示することができる。なかでも、第2剤の水性媒体中で容易に崩壊させる観点から、ゼラチン、寒天等を用いるのが好ましい。 When the contents of the first agent are softly encapsulated as an inclusion substance, the capsule wall membrane is not particularly limited as long as it can be encapsulated, and examples thereof include gelatin, agar, carrageenan, and starch. Of these, gelatin, agar and the like are preferably used from the viewpoint of easy disintegration in the aqueous medium of the second agent.
尚、カプセルの壁膜体の材質が、水性媒体中でのみ容易に崩壊する材質が好ましいことから、第1剤中のカプセルに内包させる成分に、実質的に水を含有しないことが好ましい。本発明における「実質的に水を含有しない」とは、「別途、水を含有させることはしない」という意味であり、各配合成分に含まれる微量の水の配合までを除外するものではない。 In addition, since the material of the capsule wall membrane is preferably a material that easily disintegrates only in an aqueous medium, it is preferable that the component contained in the capsule in the first agent does not substantially contain water. In the present invention, “substantially does not contain water” means “not to contain water separately” and does not exclude the addition of a trace amount of water contained in each compounding component.
次に、本発明の第2剤について説明する。本発明に係る第2剤には、必須成分として過酸化水素を含有する。 Next, the second agent of the present invention will be described. The second agent according to the present invention contains hydrogen peroxide as an essential component.
第2剤中の過酸化水素の含有量は、本発明の効果を発揮すれば特に限定されないが、脱色性の観点から、0.01質量%以上が好ましく、0.1質量%以上がより好ましい。また、皮膚刺激や毛髪の損傷を防止する観点から、12質量%以下が好ましく、6質量%以下がより好ましい。これらのことから、第2剤中の酸化剤の含有量は、0.01〜12質量%とすることが好ましく、より好ましくは0.1〜6質量%とするとよい。 The content of hydrogen peroxide in the second agent is not particularly limited as long as the effect of the present invention is exhibited, but from the viewpoint of decolorization, 0.01% by mass or more is preferable, and 0.1% by mass or more is more preferable. . Moreover, from a viewpoint of preventing skin irritation and hair damage, 12 mass% or less is preferable and 6 mass% or less is more preferable. From these things, it is preferable that content of the oxidizing agent in a 2nd agent shall be 0.01-12 mass%, More preferably, it is good to set it as 0.1-6 mass%.
本発明の第2剤は、第1剤のカプセルを容易に崩壊させる観点から、水を含有して水性媒体を分散媒とすることが好ましい。用いる水は、通常、精製水であり、イオン交換水、水道水等であっても良い。 The second agent of the present invention preferably contains water and an aqueous medium as a dispersion medium from the viewpoint of easily disintegrating the capsule of the first agent. The water used is usually purified water, and may be ion exchange water, tap water, or the like.
第2剤中の水の含有量は、本発明の効果を発揮すれば特に限定されないが、第1剤のカプセルの崩壊を容易にする観点から、50質量%以上が好ましく、80質量%以上がより好ましい。また、第2剤に過酸化水素のみを配合することを考慮すると、99.99質量%以下が好ましく、99.9質量%以下がより好ましい。これらのことから、第2剤中の水の含有量は、好ましくは50〜99.99質量%であり、より好ましくは80〜99.9質量%である。 The content of water in the second agent is not particularly limited as long as the effects of the present invention are exhibited, but from the viewpoint of facilitating the disintegration of the capsule of the first agent, 50% by mass or more is preferable, and 80% by mass or more is preferable. More preferred. In consideration of blending only hydrogen peroxide with the second agent, it is preferably 99.99% by mass or less, and more preferably 99.9% by mass or less. From these things, content of the water in a 2nd agent becomes like this. Preferably it is 50-99.99 mass%, More preferably, it is 80-99.9 mass%.
本発明の第2剤には、酸化剤の安定剤を含有させることができる。例えば、フェナセチン、ヒドロキシエタンジホスホン酸等を例示することができる。 The second agent of the present invention may contain an oxidizing agent stabilizer. For example, phenacetin, hydroxyethane diphosphonic acid and the like can be exemplified.
また、本発明に係る第2剤には、本発明の目的の効果を損なわない範囲であれば、上記した成分のほか、エタノール、イソプロパノール等の低級アルコール;ラウリルアルコール、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等の高級アルコール;ラウリン酸、ミリスチン酸、ステアリン酸、オレイン酸等の高級脂肪酸;流動パラフィン、流動イソパラフィン、スクワラン等の炭化水素;ミリスチン酸ミリスチル、ミリスチン酸イソステアリル、ステアリン酸ステアリル等のエステル;アボガド油、オリーブ油、サフラワー油、硬化油等の動植物油;ポリエチレングリコール、グリセリン、ポリグリセリン、1,3−ブチレングリコール、1,2−ペンタンジオール、1,2−オクタンジオール等の多価アルコール;ソルビタン脂肪酸エステル、グリセリン脂肪酸エステル、及びこれらのアルキレンオキシド付加物、ポリグリセリン脂肪酸エステル、ポリオキシアルキレンアルキルエーテル、ポリオキシアルキレン脂肪酸エステル、ポリオキシエチレン硬化ヒマシ油、ポリオキシエチレンラノリン等のノニオン性界面活性剤;高級脂肪酸石鹸、アルキル硫酸エステル塩、アルキルリン酸塩、ポリオキシエチレンアルキルエーテル硫酸塩、アルキルエーテルリン酸エステル、アルキルエーテルカルボン酸塩、アシルメチルタウリン塩、アルキルスルホコハク酸及びその塩等のアニオン性界面活性剤;アルキルグリシン塩、カルボキシメチルグリシン塩、N−アシルアミノエチル−N−2−ヒドロキシエチルグリシン塩等のグリシン型両性界面活性剤、アルキルアミノプロピオン酸塩、アルキルイミノジプロピオン酸塩等のアミノプロピオン酸型両性界面活性剤、アルキルジメチルアミノ酢酸ベタイン、脂肪酸アミドプロピルジメチルアミノ酢酸ベタイン等のアミノ酢酸ベタイン型両性界面活性剤、アルキルヒドロキシスルホベタイン等のスルホベタイン型両性界面活性剤等の両性界面活性剤;塩化ラウリ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、塩化ジステアリルジメチルアンモニウムなどのアルキルアミン塩;ミリスチン酸ジメチルアミノエチルアミド、ステアリン酸ジエチルアミノプロピルアミドなどの脂肪酸アミドアミン等のカチオン性界面活性剤;増粘剤、着色剤、香料等を目的に応じて適宜含有させることができる。 In addition, the second agent according to the present invention includes, in addition to the above components, lower alcohols such as ethanol and isopropanol; lauryl alcohol, myristyl alcohol, cetyl alcohol, stearyl, as long as the effects of the present invention are not impaired. Higher alcohols such as alcohol; higher fatty acids such as lauric acid, myristic acid, stearic acid and oleic acid; hydrocarbons such as liquid paraffin, liquid isoparaffin and squalane; esters such as myristyl myristate, isostearyl myristate and stearyl stearate; Animal and vegetable oils such as avocado oil, olive oil, safflower oil, hydrogenated oil; polyhydric alcohols such as polyethylene glycol, glycerin, polyglycerin, 1,3-butylene glycol, 1,2-pentanediol, 1,2-octanediol; Seo Nonionic surfactants such as bitane fatty acid esters, glycerin fatty acid esters and their alkylene oxide adducts, polyglycerin fatty acid esters, polyoxyalkylene alkyl ethers, polyoxyalkylene fatty acid esters, polyoxyethylene hydrogenated castor oil, polyoxyethylene lanolin Agents: Anions such as higher fatty acid soaps, alkyl sulfates, alkyl phosphates, polyoxyethylene alkyl ether sulfates, alkyl ether phosphates, alkyl ether carboxylates, acylmethyl taurates, alkyl sulfosuccinic acids and their salts Glycine type amphoteric surfactants such as alkyl glycine salts, carboxymethyl glycine salts, N-acylaminoethyl-N-2-hydroxyethyl glycine salts, alkyl amines Aminopropionic acid type amphoteric surfactants such as nopropionate and alkyliminodipropionate, aminoacetic acid betaine type amphoteric surfactants such as alkyldimethylaminoacetic acid betaine and fatty acid amidopropyldimethylaminoacetic acid betaine, alkylhydroxysulfobetaine Amphoteric surfactants such as sulfobetaine-type amphoteric surfactants such as; alkylamine salts such as lauryltrimethylammonium chloride, stearyltrimethylammonium chloride, distearyldimethylammonium chloride; dimethylaminoethylamide myristate, diethylaminopropylamide stearate, etc. Cationic surfactants such as fatty acid amidoamines; thickeners, colorants, fragrances and the like can be appropriately contained depending on the purpose.
本発明に係る第2剤の剤型としては、液状、ジェル状、クリーム状等の種々の剤型で用いることができ、第1剤のカプセル剤を容易に分散させる観点から、液状、ジェル状等の流動性を有する剤型であることが好ましい。 As the dosage form of the second agent according to the present invention, it can be used in various dosage forms such as liquid, gel, cream, etc. From the viewpoint of easily dispersing the capsule of the first agent, the liquid, gel It is preferable that the dosage form has fluidity such as the above.
本発明の毛髪処理剤を用いる場合、使用時に第1剤と第2剤とを混合して用いれば良いが、好ましくは、流動性を有する第2剤が充填されたアプリケータ容器に、カプセル化された第1剤を投入し、容器を密封して上下等に強く振とうする。これにより、第1剤のカプセルが第2剤中の分散媒により崩壊し、第1剤と第2剤とを容易に混合することができる。尚、第1剤にミニカプセルを用いる場合、アルカリ剤や酸化染毛剤が前記所定量配合されれば良く、第1剤に用いるミニカプセルの個数は、1個であっても良く2個以上としても良い。 When using the hair treatment agent of the present invention, the first agent and the second agent may be mixed and used at the time of use, but preferably encapsulated in an applicator container filled with a fluid second agent. The prepared first agent is added, the container is sealed, and shaken strongly up and down. Thereby, the capsule of the 1st agent can be disintegrated by the dispersion medium in the 2nd agent, and the 1st agent and the 2nd agent can be mixed easily. In addition, when using a minicapsule for the first agent, the alkali agent and the oxidative hair dye need only be mixed in the predetermined amount, and the number of minicapsules used for the first agent may be one or more than two. It is also good.
以下、本発明を実施例に基づいて更に詳細に説明するが、本発明はかかる実施例のみに限定されるものではない。尚、配合量は特記しない限り、質量%である。 EXAMPLES Hereinafter, although this invention is demonstrated further in detail based on an Example, this invention is not limited only to this Example. The blending amount is mass% unless otherwise specified.
(製造例1:毛髪脱色剤「第1剤A」)
ゼラチン85質量%、デンプン10質量%、グリセリン5質量%を加熱溶解し均一化した後、約0.3mmのゲル状シートに成型し、ソフトカプセルの壁膜体とした。一方、下記組成の粉末及び油剤を撹拌均一化した懸濁液を常法により調製しカプセル内容物とした。これらを用い、打ち抜き法により直径約2.5cm(一粒8g)の球状のソフトカプセルを調製した。得られたソフトカプセルを、毛髪脱色剤の「第1剤A」とした。尚、このカプセルの内容物の重さは、7.7gである。
(Production Example 1: Hair bleaching agent “first agent A”)
Gelatin 85% by mass, starch 10% by mass and glycerin 5% by mass were dissolved by heating and homogenized, and then molded into a gel sheet of about 0.3 mm to obtain a soft capsule wall membrane. On the other hand, a suspension obtained by stirring and homogenizing powders and oils having the following composition was prepared by a conventional method to obtain capsule contents. Using these, spherical soft capsules having a diameter of about 2.5 cm (8 g per tablet) were prepared by a punching method. The obtained soft capsule was designated as “first agent A” as a hair bleaching agent. The weight of the capsule contents is 7.7 g.
(1)ケイ酸ナトリウム 20.0
(2)炭酸マグネシウム 15.0
(3)炭酸ナトリウム 5.0
(4)塩化ナトリウム 3.0
(5)ポリオキシエチレン(50)ラノリン 5.0
(6)メチルポリシロキサン(20cs) 残 部
合 計 100.0
(1) Sodium silicate 20.0
(2) Magnesium carbonate 15.0
(3) Sodium carbonate 5.0
(4) Sodium chloride 3.0
(5) Polyoxyethylene (50) lanolin 5.0
(6) Methyl polysiloxane (20cs) balance
Total 100.0
(製造例2:毛髪脱色剤「第1剤B」)
一般的なブースター(促進剤)を含有した粉末状の毛髪脱色剤第1剤(下記組成)を、常法により調製した。得られた第1剤を、毛髪脱色剤「第1剤B」とした。
(Production Example 2: Hair bleaching agent “first agent B”)
The powdery hair bleaching agent 1st agent (following composition) containing the general booster (accelerator) was prepared by the conventional method. The obtained 1st agent was made into the hair decoloring agent "1st agent B".
(1)ケイ酸ナトリウム 3.0
(2)炭酸マグネシウム 10.0
(3)過硫酸アンモニウム 30.0
(4)過硫酸カリウム 30.0
(5)メタケイ酸ナトリウム 15.0
(6)塩化ナトリウム 10.0
(7)タルク 2.0
合 計 100.0
(1) Sodium silicate 3.0
(2) Magnesium carbonate 10.0
(3) Ammonium persulfate 30.0
(4) Potassium persulfate 30.0
(5) Sodium metasilicate 15.0
(6) Sodium chloride 10.0
(7) Talc 2.0
Total 100.0
(製造例3:毛髪脱色剤「第1剤C」)
一般的な二剤式毛髪脱色剤のクリーム状の第1剤(下記組成)を、常法により調製した。得られた第1剤を、毛髪脱色剤「第1剤C」とした。
(Production Example 3: Hair bleaching agent “first agent C”)
The creamy 1st agent (following composition) of a general two-component hair bleach was prepared by the conventional method. The obtained 1st agent was made into the hair decoloring agent "1st agent C".
(1)28%アンモニア水 10.0
(2)リン酸ジセチル 1.0
(3)ポリオキシエチレン(40)セチルエーテル 1.0
(4)ポリオキシエチレン(20)セチルエーテル 1.0
(5)メチルポリシロキサン 0.5
(6)セチルアルコール 5.0
(7)ポリエチレングリコール20000 1.0
(8)精製水 残 部
合 計 100.0
(1) 28% ammonia water 10.0
(2) Dicetyl phosphate 1.0
(3) Polyoxyethylene (40) cetyl ether 1.0
(4) Polyoxyethylene (20) cetyl ether 1.0
(5) Methyl polysiloxane 0.5
(6) Cetyl alcohol 5.0
(7) Polyethylene glycol 20000 1.0
(8) Balance of purified water
Total 100.0
(製造例4:酸化染毛剤「第1剤D」)
ゼラチン85質量%、デンプン10質量%、グリセリン5質量%を加熱溶解し均一化した後、約0.3mmのゲル状シートに成型し、ソフトカプセルの壁膜体とした。一方、下記組成の粉末及び油剤を撹拌均一化した懸濁液を常法により調製しカプセル内容物とした。これらを用い、打ち抜き法により直径約2.5cm(一粒8g)の球状のソフトカプセルを調製した。得られたソフトカプセルを、酸化染毛剤の「第1剤D」とした。尚、このカプセルの内容物の重さは、7.7gである。
(Production Example 4: Oxidative hair dye “first agent D”)
Gelatin 85% by mass, starch 10% by mass and glycerin 5% by mass were dissolved by heating and homogenized, and then molded into a gel sheet of about 0.3 mm to obtain a soft capsule wall membrane. On the other hand, a suspension obtained by stirring and homogenizing powders and oils having the following composition was prepared by a conventional method to obtain capsule contents. Using these, spherical soft capsules having a diameter of about 2.5 cm (8 g per tablet) were prepared by a punching method. The obtained soft capsule was designated as “first agent D” of the oxidative hair dye. The weight of the capsule contents is 7.7 g.
(1)ケイ酸ナトリウム 20.0
(2)炭酸マグネシウム 15.0
(3)炭酸ナトリウム 5.0
(4)硫酸トルエン2,5−ジアミン 1.0
(5)パラアミノフェノール 1.0
(6)5−アミノオルトクレゾール 2.0
(7)ポリオキシエチレン(50)ラノリン 5.0
(8)メチルポリシロキサン(20cs) 残 部
合 計 100.0
(1) Sodium silicate 20.0
(2) Magnesium carbonate 15.0
(3) Sodium carbonate 5.0
(4) Toluene sulfate 2,5-diamine 1.0
(5) Paraaminophenol 1.0
(6) 5-aminoorthocresol 2.0
(7) Polyoxyethylene (50) lanolin 5.0
(8) Methyl polysiloxane (20cs) balance
Total 100.0
(製造例5:酸化染毛剤「第1剤E」)
一般的な二剤式酸化染毛剤のクリーム状の第1剤(下記組成)を、常法により調製した。得られた第1剤を、酸化染毛剤「第1剤E」とした。
(Production Example 5: Oxidative hair dye “first agent E”)
A general two-component oxidative hair dye cream-like first agent (the following composition) was prepared by a conventional method. The obtained first agent was designated as an oxidation hair dye “first agent E”.
(1)28%アンモニア水 10.0
(2)リン酸ジセチル 1.0
(3)ポリオキシエチレン(40)セチルエーテル 1.0
(4)ポリオキシエチレン(20)セチルエーテル 1.0
(5)メチルポリシロキサン 0.5
(6)セチルアルコール 5.0
(7)硫酸トルエン2,5−ジアミン 0.3
(8)パラアミノフェノール 0.3
(9)5−アミノオルトクレゾール 0.6
(10)精製水 残 部
合 計 100.0
(1) 28% ammonia water 10.0
(2) Dicetyl phosphate 1.0
(3) Polyoxyethylene (40) cetyl ether 1.0
(4) Polyoxyethylene (20) cetyl ether 1.0
(5) Methyl polysiloxane 0.5
(6) Cetyl alcohol 5.0
(7) Toluene sulfate 2,5-diamine 0.3
(8) Paraaminophenol 0.3
(9) 5-Aminoorthocresol 0.6
(10) Purified water balance
Total 100.0
(製造例6:毛髪処理剤第2剤A)
一般的な二剤式毛髪脱色剤又は二剤式酸化染毛剤に用いられる液状の第2剤(下記組成)を、常法により調製した。得られた毛髪処理剤の第2剤を、毛髪処理剤「第2剤A」とした。
(Production Example 6: Hair Treatment Agent Second Agent A)
The liquid 2nd agent (following composition) used for a general two-component hair bleaching agent or two-component oxidative hair dye was prepared by the conventional method. The second agent of the obtained hair treatment agent was designated as a hair treatment agent “second agent A”.
(1)過酸化水素水(35%) 16.7
(2)ヒドロキシエタンジホスホン酸 0.1
(3)精製水 残 部
合 計 100.0
(1) Hydrogen peroxide solution (35%) 16.7
(2) Hydroxyethanediphosphonic acid 0.1
(3) Balance of purified water
Total 100.0
〔実験例1:毛髪脱色剤試料の調製〕
毛髪脱色剤の態様で、以下の検討を実施した。すなわち、アプリケータ容器に充填された毛髪処理剤「第2剤A」70gに、毛髪脱色剤「第1剤A」のソフトカプセル1個(8g)を投入し、容器を密封して上下に30回上下に振とうした。この毛髪処理剤を、「実施例1」とした。
アプリケータ容器に充填された毛髪処理剤「第2剤A」4質量部に対し、毛髪脱色剤「第1剤B」1質量部を投入し、容器を密封して上下に30回上下に振とうした。この毛髪処理剤を、「比較例1」とした。
また、アプリケータ容器に充填された毛髪処理剤「第2剤A」2質量部に対し、毛髪脱色剤「第1剤C」1質量部を投入し、容器を密封して上下に30回上下に振とうした。この毛髪処理剤を、「比較標準品1」とした。
[Experimental Example 1: Preparation of hair bleaching agent sample]
The following examination was carried out in the form of a hair bleaching agent. That is, one soft capsule (8 g) of the hair bleaching agent “first agent A” is put into 70 g of the hair treatment agent “second agent A” filled in the applicator container, and the container is sealed 30 times up and down. Shake up and down. This hair treatment agent was designated “Example 1”.
1 part by weight of the hair bleaching agent “First Agent B” is added to 4 parts by weight of the hair treatment agent “Second Agent A” filled in the applicator container, and the container is sealed and shaken up and down 30 times. That ’s it. This hair treatment agent was designated “Comparative Example 1”.
In addition, 1 part by weight of the hair bleaching agent “First Agent C” is added to 2 parts by weight of the hair treatment agent “Second Agent A” filled in the applicator container, and the container is sealed up and down 30 times. Shake to. This hair treatment agent was designated as “Comparative Standard 1”.
(試験例1:使用性の評価)
上記第1剤の投入時に、第1剤の舞い散る程度を、比較標準品1と比較し下記評価基準に基づいて評価した。また、振とう時の混合の容易性について、下記評価基準に基づいて評価した。それぞれの結果を表1に記す。
(Test Example 1: Evaluation of usability)
When the first agent was introduced, the degree to which the first agent was scattered was compared with the comparative standard product 1 and evaluated based on the following evaluation criteria. Moreover, the ease of mixing at the time of shaking was evaluated based on the following evaluation criteria. The results are shown in Table 1.
<舞い散りの評価基準>
○:比較標準品1と同様に第1剤の舞い散りが全くない。
△:比較標準品1に比べ第1剤の舞い散りが僅かにある。
×:比較標準品1に比べ第1剤の舞い散りがある。
<Evaluation criteria for dance>
○: As in Comparative Standard Product 1, there is no scattering of the first agent.
(Triangle | delta): Compared with the comparison standard product 1, there is slight scattering of the 1st agent.
X: Compared with the comparative standard product 1, there is scattering of the first agent.
<混合性の評価基準>
○:比較標準品1と同様に均一に混合される。
△:比較標準品1に比べ僅かに均一に混合されない。
×:比較標準品1に比べ均一に混合されない。
<Mixability evaluation criteria>
◯: Same as the comparative standard product 1, mixed uniformly.
(Triangle | delta): Compared with the comparison standard goods 1, it is not mixed slightly uniformly.
X: Not uniformly mixed as compared with Comparative Standard Product 1.
(試験例2:脱色性の評価)
試験例1で混合して得た各毛髪処理剤2gを、重さ1g、長さ10cmの黒色人毛毛束に均一に塗布し、30℃の雰囲気下で30分間放置した。その後、水で洗浄し、ドライヤーを用いて毛束を乾燥して脱色毛束を得た。得られた各脱色毛束の脱色の程度を、比較標準品1と隣接比較して下記評価基準に基づいて評価した。結果を表1に記す。
(Test Example 2: Decolorization evaluation)
2 g of each hair treatment agent obtained by mixing in Test Example 1 was uniformly applied to a black human hair bundle having a weight of 1 g and a length of 10 cm, and was left in an atmosphere at 30 ° C. for 30 minutes. Then, it washed with water and dried the hair | bristle bundle using the drier, and obtained the decoloring hair | bristle bundle. The degree of decolorization of each of the obtained decolorized hair bundles was adjacently compared with the comparative standard product 1 and evaluated based on the following evaluation criteria. The results are shown in Table 1.
<評価基準>
○:比較標準品1より毛髪が明らかに脱色されている。
△:比較標準品1より僅かに毛髪が脱色されている。
×:比較標準品1と同等に毛髪が脱色されている。
<Evaluation criteria>
○: The hair is clearly decolorized from the comparative standard product 1.
(Triangle | delta): The hair is decolored slightly from the comparison reference product 1.
X: The hair is decolored as in the case of the comparative standard product 1.
表1の結果から、本発明の毛髪処理剤を毛髪脱色剤の態様で用いると、第1剤の投入時に第1剤が舞い散ることがなく、第1剤と第2剤を容易に混合できることが分かる。また、一般的な二剤式の毛髪脱色剤(比較標準品1)より脱色力に優れ、過硫酸塩などの強い酸化剤(促進剤)を用いなくとも、促進剤を用いた場合と同等以上の毛髪脱色力を発揮することが分かる。 From the results in Table 1, when the hair treatment agent of the present invention is used in the form of a hair bleaching agent, the first agent does not splash when the first agent is added, and the first agent and the second agent can be easily mixed. I understand. In addition, it is superior to general two-component hair bleaching agent (Comparative Standard Product 1) and has the same level of decolorizing power as or more than when a promoter is used without using a strong oxidizing agent (accelerator) such as persulfate. It can be seen that the hair decoloring power is exhibited.
〔実験例2:酸化染毛剤試料の調製〕
酸化染毛剤の態様で、以下の検討を実施した。すなわち、アプリケータ容器に充填された毛髪処理剤「第2剤A」70gに、酸化染毛剤「第1剤D」のソフトカプセル1個(8g)を投入し、容器を密封して上下に30回上下に振とうした。この毛髪処理剤を、「実施例2」とした。
また、アプリケータ容器に充填された毛髪処理剤「第2剤A」2質量部に対し、酸化染毛剤「第1剤E」1質量部を投入し、容器を密封して上下に30回上下に振とうした。この毛髪処理剤を、「比較標準品2」とした。
[Experimental Example 2: Preparation of oxidation hair dye sample]
The following examination was implemented in the aspect of oxidation hair dye. That is, one soft capsule (8 g) of the oxidative hair dye “first agent D” is put into 70 g of the hair treatment agent “second agent A” filled in the applicator container, and the container is sealed 30 up and down. Shake up and down times. This hair treatment agent was designated “Example 2”.
Also, for 2 parts by mass of the hair treatment agent “Second Agent A” filled in the applicator container, 1 part by mass of the hair dye “First Agent E” is charged, the container is sealed, and 30 times up and down. Shake up and down. This hair treatment agent was designated as “Comparative Standard Product 2”.
(試験例3:染料安定性)
「第1剤D」或いは「第1剤E」を、ポリプロピレン製のキャップおよびポリエチレン製の中栓のついたガラス瓶に密封し、温度40℃,湿度60%の恒温恒湿槽にて30日間保存後、染料の発色の程度を目視で観察し、下記評価基準に基づいて評価した。「第1剤D」の結果を表2に記す。尚、「第1剤E」は染料の発色が認められ、染料安定性評価は下記評価基準の「×」であった。
(Test Example 3: Dye stability)
“First Agent D” or “First Agent E” is sealed in a glass bottle with a polypropylene cap and a polyethylene stopper and stored in a constant temperature and humidity chamber at a temperature of 40 ° C. and a humidity of 60% for 30 days. Thereafter, the degree of coloring of the dye was visually observed and evaluated based on the following evaluation criteria. The results of “First Agent D” are shown in Table 2. In addition, the color development of the dye was recognized for the “first agent E”, and the dye stability evaluation was “x” of the following evaluation criteria.
<評価基準>
○:染料の発色が認められない。
△:染料の発色がわずかに認められる。
×:染料の発色が認められる。
<Evaluation criteria>
○: Color development of the dye is not recognized.
Δ: Dye coloring is slightly observed.
X: Color development of the dye is observed.
(試験例4:使用性の評価)
実験例2の第1剤と第2剤の振とう時の混合容易性について、試験例1と同様に比較標準品2と比較して評価した。結果を表2に記す。
(Test Example 4: Evaluation of usability)
The ease of mixing during shaking of the first agent and the second agent in Experimental Example 2 was evaluated in comparison with Comparative Standard Product 2 as in Test Example 1. The results are shown in Table 2.
(試験例5:染色明度の評価)
試験例4で混合して得た各毛髪処理剤2gを、重さ1g、長さ10cmの黒色人毛毛束に均一に塗布し、30℃の雰囲気下で30分間放置した。その後、水で洗浄し、ドライヤーを用いて毛束を乾燥して、赤色に染色した染色毛束を得た。得られた各染色毛束の染色の色調(明度)の程度を、比較標準品2と隣接比較して下記評価基準に基づいて評価した。結果を表2に記す。
(Test Example 5: Evaluation of dyeing lightness)
2 g of each hair treatment agent obtained by mixing in Test Example 4 was uniformly applied to a black human hair bundle having a weight of 1 g and a length of 10 cm, and was left in an atmosphere at 30 ° C. for 30 minutes. Thereafter, the hair bundle was washed with water and dried with a dryer to obtain a dyed hair bundle dyed red. The degree of color tone (lightness) of each of the obtained hair bundles was compared with that of Comparative Standard Product 2 and evaluated based on the following evaluation criteria. The results are shown in Table 2.
<評価基準>
○:比較標準品2より毛髪の明度が明らかに高い。
△:比較標準品2より僅かに毛髪の明度が高い。
×:比較標準品2と同等の毛髪の明度である。
<Evaluation criteria>
○: The lightness of the hair is clearly higher than that of Comparative Standard Product 2.
Δ: Brightness of hair is slightly higher than that of Comparative Standard Product 2.
X: The lightness of the hair is the same as that of the comparative standard product 2.
表2の結果から、本発明の毛髪処理剤を酸化染毛剤の態様で用いると、第1剤は染料安定性に優れることが分かる。また、本発明の毛髪処理剤は、第1剤と第2剤を容易に混合できることが分かる。更には、一般的な二剤式の毛髪処理剤(比較標準品2)に比べ、格段に明るい色調に染色できることが分かる。 From the results in Table 2, it can be seen that when the hair treatment agent of the present invention is used in the form of an oxidative hair dye, the first agent is excellent in dye stability. Moreover, it turns out that the hair treatment agent of this invention can mix a 1st agent and a 2nd agent easily. Furthermore, it can be seen that it can be dyed in a much brighter color tone than a general two-component hair treatment agent (Comparative Standard Product 2).
Claims (8)
前記アルカリ剤が、炭酸塩、炭酸水素塩、酒石酸塩、クエン酸塩、リン酸塩、二リン酸塩、ケイ酸塩、メタケイ酸塩、酢酸塩からなる群から選ばれる1種以上である固体のアルカリ剤である酸化染毛剤。 Ri Do from a first agent consisting of capsules containing an alkali agent, a second agent containing hydrogen peroxide,
A solid in which the alkaline agent is at least one selected from the group consisting of carbonate, bicarbonate, tartrate, citrate, phosphate, diphosphate, silicate, metasilicate, and acetate. Oxidative hair dye which is an alkaline agent .
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| JPH01193216A (en) * | 1988-01-29 | 1989-08-03 | Fuji Kapuseru Kk | Soft capsule and globular article |
| DE19755420A1 (en) * | 1997-12-13 | 1999-06-17 | Schwarzkopf Gmbh Hans | Agents for treating keratin fibers |
| DE19852611C1 (en) * | 1998-11-14 | 2000-09-07 | Wella Ag | Use of dehydroascorbic acid in fixatives and agents and methods for permanent hair shaping |
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| US20250161176A1 (en) * | 2021-09-30 | 2025-05-22 | Kao Corporation | Solid composition for dyeing keratin |
| EP4410268A4 (en) * | 2021-09-30 | 2025-09-17 | Kao Corp | SOLID COMPOSITION FOR COLORING KERATIN |
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