JPH0667820B2 - Hair modifier composition - Google Patents
Hair modifier compositionInfo
- Publication number
- JPH0667820B2 JPH0667820B2 JP61206589A JP20658986A JPH0667820B2 JP H0667820 B2 JPH0667820 B2 JP H0667820B2 JP 61206589 A JP61206589 A JP 61206589A JP 20658986 A JP20658986 A JP 20658986A JP H0667820 B2 JPH0667820 B2 JP H0667820B2
- Authority
- JP
- Japan
- Prior art keywords
- hair
- composition
- group
- aldehyde
- modifier composition
- 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
- 239000000203 mixture Substances 0.000 title claims description 35
- 239000003607 modifier Substances 0.000 title description 11
- MWOOGOJBHIARFG-UHFFFAOYSA-N vanillin Chemical compound COC1=CC(C=O)=CC=C1O MWOOGOJBHIARFG-UHFFFAOYSA-N 0.000 claims description 8
- FGQOOHJZONJGDT-UHFFFAOYSA-N vanillin Natural products COC1=CC(O)=CC(C=O)=C1 FGQOOHJZONJGDT-UHFFFAOYSA-N 0.000 claims description 8
- 235000012141 vanillin Nutrition 0.000 claims description 8
- KJPRLNWUNMBNBZ-QPJJXVBHSA-N (E)-cinnamaldehyde Chemical compound O=C\C=C\C1=CC=CC=C1 KJPRLNWUNMBNBZ-QPJJXVBHSA-N 0.000 claims description 7
- -1 alkyl aldehydes Chemical class 0.000 claims description 7
- 229940117916 cinnamic aldehyde Drugs 0.000 claims description 5
- KJPRLNWUNMBNBZ-UHFFFAOYSA-N cinnamic aldehyde Natural products O=CC=CC1=CC=CC=C1 KJPRLNWUNMBNBZ-UHFFFAOYSA-N 0.000 claims description 5
- 150000001875 compounds Chemical class 0.000 claims description 4
- 239000004480 active ingredient Substances 0.000 claims description 3
- 125000004432 carbon atom Chemical group C* 0.000 claims description 2
- 229940117960 vanillin Drugs 0.000 claims description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 15
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 13
- 239000000243 solution Substances 0.000 description 10
- 238000011282 treatment Methods 0.000 description 10
- 125000003172 aldehyde group Chemical group 0.000 description 9
- 230000000694 effects Effects 0.000 description 9
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 8
- 150000001299 aldehydes Chemical class 0.000 description 8
- 239000003795 chemical substances by application Substances 0.000 description 8
- 125000003396 thiol group Chemical group [H]S* 0.000 description 8
- 230000003648 hair appearance Effects 0.000 description 7
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 6
- 235000019441 ethanol Nutrition 0.000 description 6
- 230000009257 reactivity Effects 0.000 description 6
- 239000004359 castor oil Substances 0.000 description 5
- 235000019438 castor oil Nutrition 0.000 description 5
- 238000006243 chemical reaction Methods 0.000 description 5
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 5
- 238000005406 washing Methods 0.000 description 5
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 4
- 239000007864 aqueous solution Substances 0.000 description 4
- 239000003205 fragrance Substances 0.000 description 4
- 235000011187 glycerol Nutrition 0.000 description 4
- 238000003756 stirring Methods 0.000 description 4
- VBICKXHEKHSIBG-UHFFFAOYSA-N 1-monostearoylglycerol Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(O)CO VBICKXHEKHSIBG-UHFFFAOYSA-N 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- XUJNEKJLAYXESH-REOHCLBHSA-N L-Cysteine Chemical compound SC[C@H](N)C(O)=O XUJNEKJLAYXESH-REOHCLBHSA-N 0.000 description 3
- QNAYBMKLOCPYGJ-REOHCLBHSA-N L-alanine Chemical compound C[C@H](N)C(O)=O QNAYBMKLOCPYGJ-REOHCLBHSA-N 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- 235000004279 alanine Nutrition 0.000 description 3
- 125000000217 alkyl group Chemical group 0.000 description 3
- ZZTCCAPMZLDHFM-UHFFFAOYSA-N ammonium thioglycolate Chemical compound [NH4+].[O-]C(=O)CS ZZTCCAPMZLDHFM-UHFFFAOYSA-N 0.000 description 3
- 229940075861 ammonium thioglycolate Drugs 0.000 description 3
- 229960000541 cetyl alcohol Drugs 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- 230000003750 conditioning effect Effects 0.000 description 3
- 235000018417 cysteine Nutrition 0.000 description 3
- XUJNEKJLAYXESH-UHFFFAOYSA-N cysteine Natural products SCC(N)C(O)=O XUJNEKJLAYXESH-UHFFFAOYSA-N 0.000 description 3
- 238000004043 dyeing Methods 0.000 description 3
- BXWNKGSJHAJOGX-UHFFFAOYSA-N hexadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCO BXWNKGSJHAJOGX-UHFFFAOYSA-N 0.000 description 3
- 239000004615 ingredient Substances 0.000 description 3
- 239000002932 luster Substances 0.000 description 3
- 239000002304 perfume Substances 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- ALSTYHKOOCGGFT-KTKRTIGZSA-N (9Z)-octadecen-1-ol Chemical compound CCCCCCCC\C=C/CCCCCCCCO ALSTYHKOOCGGFT-KTKRTIGZSA-N 0.000 description 2
- RBTBFTRPCNLSDE-UHFFFAOYSA-N 3,7-bis(dimethylamino)phenothiazin-5-ium Chemical compound C1=CC(N(C)C)=CC2=[S+]C3=CC(N(C)C)=CC=C3N=C21 RBTBFTRPCNLSDE-UHFFFAOYSA-N 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- 102000011782 Keratins Human genes 0.000 description 2
- 108010076876 Keratins Proteins 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- 239000002202 Polyethylene glycol Substances 0.000 description 2
- 229920002125 Sokalan® Polymers 0.000 description 2
- 230000009471 action Effects 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- 230000008859 change Effects 0.000 description 2
- 238000013329 compounding Methods 0.000 description 2
- LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 239000000796 flavoring agent Substances 0.000 description 2
- 235000019634 flavors Nutrition 0.000 description 2
- 229940057995 liquid paraffin Drugs 0.000 description 2
- 229960000907 methylthioninium chloride Drugs 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 230000000051 modifying effect Effects 0.000 description 2
- 230000003020 moisturizing effect Effects 0.000 description 2
- 229940055577 oleyl alcohol Drugs 0.000 description 2
- XMLQWXUVTXCDDL-UHFFFAOYSA-N oleyl alcohol Natural products CCCCCCC=CCCCCCCCCCCO XMLQWXUVTXCDDL-UHFFFAOYSA-N 0.000 description 2
- 229920001223 polyethylene glycol Polymers 0.000 description 2
- 239000003531 protein hydrolysate Substances 0.000 description 2
- 235000018102 proteins Nutrition 0.000 description 2
- 108090000623 proteins and genes Proteins 0.000 description 2
- 102000004169 proteins and genes Human genes 0.000 description 2
- 238000010008 shearing Methods 0.000 description 2
- 238000002791 soaking Methods 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- CWERGRDVMFNCDR-UHFFFAOYSA-M thioglycolate(1-) Chemical compound [O-]C(=O)CS CWERGRDVMFNCDR-UHFFFAOYSA-M 0.000 description 2
- CWERGRDVMFNCDR-UHFFFAOYSA-N thioglycolic acid Chemical compound OC(=O)CS CWERGRDVMFNCDR-UHFFFAOYSA-N 0.000 description 2
- HMKKIXGYKWDQSV-SDNWHVSQSA-N 2-Pentyl-3-phenyl-2-propenal Chemical compound CCCCC\C(C=O)=C/C1=CC=CC=C1 HMKKIXGYKWDQSV-SDNWHVSQSA-N 0.000 description 1
- RFVNOJDQRGSOEL-UHFFFAOYSA-N 2-hydroxyethyl octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCCO RFVNOJDQRGSOEL-UHFFFAOYSA-N 0.000 description 1
- RRVKOWFYEYMAMH-UHFFFAOYSA-N CCO.O=CC=CC1=CC=CC=C1 Chemical compound CCO.O=CC=CC1=CC=CC=C1 RRVKOWFYEYMAMH-UHFFFAOYSA-N 0.000 description 1
- 239000004909 Moisturizer Substances 0.000 description 1
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 1
- DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- 101710172711 Structural protein Proteins 0.000 description 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
- GORMSINSWZJIKL-UHFFFAOYSA-N [3-(2-ethylhexanoyloxy)-2,2-dimethylpropyl] 2-ethylhexanoate Chemical compound CCCCC(CC)C(=O)OCC(C)(C)COC(=O)C(CC)CCCC GORMSINSWZJIKL-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- GUUHFMWKWLOQMM-NTCAYCPXSA-N alpha-hexylcinnamaldehyde Chemical compound CCCCCC\C(C=O)=C/C1=CC=CC=C1 GUUHFMWKWLOQMM-NTCAYCPXSA-N 0.000 description 1
- GUUHFMWKWLOQMM-UHFFFAOYSA-N alpha-n-hexylcinnamic aldehyde Natural products CCCCCCC(C=O)=CC1=CC=CC=C1 GUUHFMWKWLOQMM-UHFFFAOYSA-N 0.000 description 1
- 235000001014 amino acid Nutrition 0.000 description 1
- 150000001413 amino acids Chemical class 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 235000013871 bee wax Nutrition 0.000 description 1
- 239000012166 beeswax Substances 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 239000003638 chemical reducing agent Substances 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- PXBRQCKWGAHEHS-UHFFFAOYSA-N dichlorodifluoromethane Chemical compound FC(F)(Cl)Cl PXBRQCKWGAHEHS-UHFFFAOYSA-N 0.000 description 1
- 235000019404 dichlorodifluoromethane Nutrition 0.000 description 1
- 239000002552 dosage form Substances 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 229940075507 glyceryl monostearate Drugs 0.000 description 1
- 230000003699 hair surface Effects 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000006210 lotion Substances 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 230000001333 moisturizer Effects 0.000 description 1
- 239000001788 mono and diglycerides of fatty acids Substances 0.000 description 1
- FEMOMIGRRWSMCU-UHFFFAOYSA-N ninhydrin Chemical compound C1=CC=C2C(=O)C(O)(O)C(=O)C2=C1 FEMOMIGRRWSMCU-UHFFFAOYSA-N 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 1
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 230000002335 preservative effect Effects 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 235000019333 sodium laurylsulphate Nutrition 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 238000004809 thin layer chromatography Methods 0.000 description 1
- 150000003555 thioacetals Chemical class 0.000 description 1
- 229940071127 thioglycolate Drugs 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
- A61K8/35—Ketones, e.g. benzophenone
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q5/00—Preparations for care of the hair
- A61Q5/12—Preparations containing hair conditioners
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q5/00—Preparations for care of the hair
- A61Q5/06—Preparations for styling the hair, e.g. by temporary shaping or colouring
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Emergency Medicine (AREA)
- Birds (AREA)
- Epidemiology (AREA)
- Dermatology (AREA)
- Cosmetics (AREA)
Description
【発明の詳細な説明】 発明の分野 本発明は毛髪改質剤組成物に関し、さらに詳しくは、毛
髪の化学構造を変化させることにより一度の処理で毛質
が長期間に亘り改善される毛髪改質剤組成物に関する。Description: FIELD OF THE INVENTION The present invention relates to a hair modifier composition, and more particularly, to a hair modifier in which a single treatment improves the hair quality over a long period of time by changing the chemical structure of the hair. The present invention relates to a substance composition.
発明の背景 従来から、毛髪に柔軟性、艶、こし等を付与するため
に、保湿剤、コンディショニング剤等を配合した種々の
毛髪処理剤が使用されている。しかし、これらの毛髪処
理剤は保湿剤、コンディショニング剤等の毛髪表面への
吸着により効果が発現されるものであり、洗髪等により
その効果が容易に消失してしまう一時的処理に過ぎな
い。したがって、特に整髪に多くの時間と労力を要して
いる剛質毛や軟質毛の人々にとっては、洗髪等の度に煩
わしい処理を繰り返さねばならず、このような毛髪処理
剤は到底満足の出来るものではない。そこで一度の処理
で毛質が長期間に亘り改善され、容易に整髪可能となる
ような毛髪改質剤組成物の開発が要望されている。BACKGROUND OF THE INVENTION Various hair treating agents containing a moisturizing agent, a conditioning agent and the like have been used in the past in order to impart flexibility, luster, strain and the like to hair. However, these hair treatment agents exhibit their effects by adsorbing moisturizing agents, conditioning agents and the like to the hair surface, and are only temporary treatments where the effects are easily lost by washing the hair. Therefore, especially for people with bristly hair or soft hair, which requires a lot of time and labor for hair styling, a troublesome treatment must be repeated every time hair is washed, and such a hair treatment agent is completely satisfactory. Not a thing. Therefore, there is a demand for the development of a hair modifier composition that improves hair quality for a long period of time by a single treatment and that allows easy hair styling.
本発明者らは、かかる現状に鑑み毛質改善について鋭意
検討した結果、分子構造中に特定の基を有する特定の化
合物を有効成分として配合した組成物によれば、一度の
毛髪処理で毛質が長期間に亘り改善され、柔軟性、艶、
こし等を有する整髪し易い毛髪となることを見出し、本
発明を完成するに至った。As a result of intensive studies on hair quality improvement in view of the present situation, the present inventors have found that a composition containing a specific compound having a specific group in its molecular structure as an active ingredient can provide hair quality with a single hair treatment. Is improved over a long period of time, and has flexibility, luster,
The present invention has been completed by discovering that hair having a brush and the like can be easily adjusted.
発明の開示 本発明は、分子構造中にアルデヒド基とともに直鎖アル
キル基または芳香族基を有する化合物を有効成分として
含有することを特徴とする毛髪改質組成物を提供する。DISCLOSURE OF THE INVENTION The present invention provides a hair-modifying composition comprising a compound having a linear alkyl group or an aromatic group in the molecular structure together with an aldehyde group as an active ingredient.
本発明の毛質改質剤組成物によれば、一度の処理で毛質
が長期間に亘り改善され、柔軟性、艶、こし等を有する
整髪し易い毛髪とすることができる。これは毛髪タンパ
ク中のチオール基と本発明組成物の配合成分中のアルデ
ヒド基との化学反応に起因するものと推定される。According to the hair quality modifier composition of the present invention, the hair quality is improved for a long period of time by a single treatment, and it is possible to obtain hair that has softness, luster, firmness, etc. and is easy to prepare. It is presumed that this is due to a chemical reaction between the thiol group in the hair protein and the aldehyde group in the formulation component of the composition of the present invention.
本発明に用いられる分子構造中にアルデヒド基とともに
直鎖アルキル基または芳香族基を有する化合物として
は、バニリン、シンナムアルデヒド、シンナムアルデヒ
ド誘導体またはアルキルアルデヒド等、好ましくは、バ
ニリン、シンナムアルデヒド、ヘキシルシンナムアルデ
ヒド、アミルシンナムアルデヒドまたは直鎖アルキルア
ルデヒド(アルキルの炭素数8〜22)が挙げられる。配
合量は、組成物全量に対して0.5〜20重量%、好ましく
は1.0〜10重量%とするのが望ましい。配合量が0.5重量
%より少ないと所期の効果が得られず、一方、20重量%
より多いとアルデヒド類特有の臭いのため実用的ではな
い。The compound having a linear alkyl group or an aromatic group together with an aldehyde group in the molecular structure used in the present invention includes vanillin, cinnamaldehyde, cinnamaldehyde derivatives or alkylaldehyde, and preferably vanillin, cinnamaldehyde, hexylcinnamaldehyde. , Amylcinnamaldehyde or linear alkyl aldehyde (alkyl has 8 to 22 carbon atoms). The blending amount is 0.5 to 20% by weight, preferably 1.0 to 10% by weight based on the total amount of the composition. If the amount is less than 0.5% by weight, the desired effect cannot be obtained, while on the other hand, 20% by weight
If the amount is larger, the odor peculiar to aldehydes is not practical.
本発明の毛髪改質剤組成物は、各成分を適宜混合、溶解
し、常法に従って、ローション、乳液、フォーム等の剤
形とすることができ、さらに、所望により、本発明の効
果を損なわない範囲で、可溶化剤、乳化剤、香料、着色
剤、防腐剤、コンディショニング剤、保湿剤等を配合し
てもよい。The hair modifier composition of the present invention can be prepared by appropriately mixing and dissolving the respective components to prepare a dosage form such as lotion, emulsion or foam according to a conventional method, and further, if desired, impairing the effects of the present invention. You may mix | blend a solubilizer, an emulsifier, a fragrance | flavor, a coloring agent, a preservative, a conditioning agent, a moisturizer etc. in the range which does not exist.
本発明の毛髪改質剤組成物の使用方法としては、例え
ば、洗髪後の毛髪に塗布した後、一定時間放置し洗い流
すか、またはチオグリコール酸等の還元で処理した後の
毛髪に塗布し、一定時間放置した後洗い流すこと等が挙
げられる。なお、放置の間に若干加熱してもよい。As a method of using the hair modifier composition of the present invention, for example, after applying to hair after washing, it is left standing for a certain period of time to wash away, or applied to hair after being treated with reduction of thioglycolic acid or the like, For example, it may be washed after leaving it for a certain period of time. In addition, you may heat slightly while leaving.
実験 つぎに毛髪の構造タンパク質であるケラチンの構成アミ
ノ酸であるアラニン、システインおよびその誘導体とア
ルデヒド基の反応性ならびに毛髪内に存在するチオール
基とアルデヒド基の反応性について試験した結果を示
す。Experiment Next, the results of tests on the reactivity of aldehyde groups with alanine, cysteine and its derivatives, which are the constituent amino acids of keratin, which is a structural protein of hair, and the reactivity of thiol groups and aldehyde groups present in hair are shown.
(1)アラニン、システインおよびその誘導体とアルデ
ヒド基の反応性 アラニン、システインまたはその誘導体1ミリモルをエ
タノールまたは水2.5mlに溶解した。これにバニリン1
ミリモルをエタノール2.5mlに溶解した溶液を撹拌下、
室温にて加えた。20分後、展開溶媒としてn−ブタノー
ル/酢酸/水(4:1:1)を用い、薄層クロマトグラフィ
ーに付した後ニンヒドリンで発色させ、反応前後のスポ
ットのRf値を比較し、以下の基準により反応性を調べ
た。(1) Reactivity of alanine, cysteine and its derivative with aldehyde group 1 mmol of alanine, cysteine or its derivative was dissolved in 2.5 ml of ethanol or water. Vanillin 1
While stirring a solution of millimoles dissolved in 2.5 ml of ethanol,
Added at room temperature. After 20 minutes, using n-butanol / acetic acid / water (4: 1: 1) as a developing solvent, the mixture was subjected to thin-layer chromatography and then developed with ninhydrin, and the Rf values of the spots before and after the reaction were compared. Reactivity was checked by standard.
反応性有:反応後、新たなRf値のスポットが出現した。Reactive: A spot with a new Rf value appeared after the reaction.
反応性無:反応前後でスポットのRf値に変化がなかっ
た。No reactivity: The Rf value of the spot did not change before and after the reaction.
結果を第1表に示す。The results are shown in Table 1.
表1から明らかなように、アルデヒド基はチオール基と
反応し、アミノ基、カルボキシル基またはメチル基とは
反応しない。毛髪中のケラチンタンパクにおいても同様
の反応が生じているものと考えられる。 As is clear from Table 1, the aldehyde group reacts with the thiol group and does not react with the amino group, the carboxyl group or the methyl group. It is considered that the same reaction occurs in the keratin protein in hair.
(2)毛髪内に存在するチオール基とアルデヒド基の反
応性 6.7%チオグリコール酸アンモニウム水溶液50ml(pH8.
6)に毛髪2g(日本人女子の頭髪)を10分間浸漬し、つ
いで、水、5%クエン酸溶液、水で洗浄した後バニリン
またはシンナムアルデヒドのエタノール溶液50mlに10分
間浸漬した。水洗後タオルドライし、0.14%メチレンブ
ルー溶液に5分間浸漬した後、再び水洗した。得られた
染色毛を2mμの厚さに切断して断面を光学顕微鏡で観察
し、染色度合を調べた。比較として処理する前の毛髪お
よび6.7%チオグリコール酸アンモニウム水溶液に10分
間浸漬した後の毛髪についても染色度合を調べた。結果
を第2表に示す。(2) Reactivity of thiol groups and aldehyde groups present in hair 6.7% ammonium thioglycolate aqueous solution 50 ml (pH 8.
2 g of hair (hair of a Japanese girl) was soaked in 6) for 10 minutes, then washed with water, 5% citric acid solution, and water, and then soaked in 50 ml of vanillin or cinnamaldehyde ethanol solution for 10 minutes. After washing with water, it was towel-dried, immersed in a 0.14% methylene blue solution for 5 minutes, and then washed again with water. The obtained dyed hair was cut to a thickness of 2 mμ and the cross section was observed with an optical microscope to examine the degree of dyeing. As a comparison, the degree of dyeing was also examined for the hair before treatment and the hair after soaking in the 6.7% ammonium thioglycolate aqueous solution for 10 minutes. The results are shown in Table 2.
毛髪構成タンパク中には多数のジスルフイド結合が存在
し、チオグリコール酸塩などの還元剤で毛髪を処理する
ことにより該結合が開裂してチオール基が生成する。か
かるチオール基は還元性基であり、メチレンブルー存在
下に毛髪を染色する(処理番号2参照)。ところが、第
2表から明らかなようにチオグリコール酸塩で処理した
毛髪をさらにアルデヒド類で処理すると染色度合が減少
し、遊離のチオール基の存在が減少したことがわかる。
このことは実験(1)の結果と共にチオール基がアルデ
ヒド基と反応していることを示しており、式: で示されるチオアセタールを形成するものと推定され
る。かかる化学変化に起因するため、本発明の組成物に
より生じる毛質の変化は長期間接続する。 Many disulphide bonds are present in the hair-constituting protein, and when the hair is treated with a reducing agent such as thioglycolate, the bonds are cleaved to generate a thiol group. Such a thiol group is a reducing group and dyes hair in the presence of methylene blue (see treatment number 2). However, as is clear from Table 2, when hair treated with thioglycollate is further treated with aldehydes, the degree of dyeing is reduced and the presence of free thiol groups is reduced.
This indicates that the thiol group is reacting with the aldehyde group together with the result of the experiment (1). It is presumed that the thioacetal represented by is formed. Due to such chemical changes, the changes in hair quality caused by the composition of the present invention are connected for a long period of time.
実施例 つぎに実施例を挙げて本発明をさらに詳しく説明する。EXAMPLES Next, the present invention will be described in more detail with reference to Examples.
実施例1〜17 成分 重量% アルデヒド誘導体(第3表に記載) 第3表に記載 ポリオキシエチレン硬化ヒマシ油 0.3 グリセリン 1.5 95%エチルアルコール 60.0 香料 適量 イオン交換水 100に調整 香料をポリオキシエチレン硬化ヒマシ油に溶解し、第3
表に記載したアルデヒド誘導体および95%エチルアルコ
ールの溶液中に加え、充分撹拌する。ついで、グリセリ
ンおよびイオン交換水を加え、さらに撹拌して毛髪改質
剤組成物を製造する。Examples 1 to 17 Ingredients% by weight Aldehyde derivative (described in Table 3) Described in Table 3 Polyoxyethylene hydrogenated castor oil 0.3 Glycerin 1.5 95% Ethyl alcohol 60.0 Fragrance Suitable amount Ion-exchanged water 100 Adjusted perfume to polyoxyethylene Third, dissolved in castor oil
Add to the solution of the aldehyde derivative shown in the table and 95% ethyl alcohol and stir well. Then, glycerin and ion-exchanged water are added, and the mixture is further stirred to produce a hair modifier composition.
このようにして得られた組成物を用いて処理した毛髪の
評価を行なった。The hair treated with the composition thus obtained was evaluated.
すなわち、20gの毛髪スワッチ(同一日本人女子の頭
髪)を6.7%チオグリコール酸アンモニウム溶液(アン
モニアでpH8.6に調整)200mlに15分間浸漬した。ついで
水洗し、タオルドライし、前記の組成物の溶液200mlに1
5分間浸漬した後、(1)充分に濯ぎ乾燥するか、また
は(2)10%ラウリル硫酸ナトリウム溶液で5回洗浄
し、充分に濯ぎ乾燥した。That is, 20 g of hair swatch (hair of the same Japanese girl) was immersed in 200 ml of a 6.7% ammonium thioglycolate solution (adjusted to pH 8.6 with ammonia) for 15 minutes. Then rinse with water, dry with a towel, and add 1 to 200 ml of the above composition.
After soaking for 5 minutes, (1) it was thoroughly rinsed and dried, or (2) it was washed 5 times with a 10% sodium lauryl sulfate solution and thoroughly rinsed and dried.
ついで、アルデヒド誘導体を配合しない以外前記と同じ
処方で調製した溶液を用いて前記と同様の処理を行なっ
た毛髪スワッチを対照として毛質軟化、毛質硬化、弾力
性、しなやかさおよび滑沢性の程度について以下の基準
に従い専門パネラーに4段階で評価させた。Then, using a solution prepared in the same manner as described above except that an aldehyde derivative was not added, a hair swatch treated in the same manner as described above was used as a control for softening hair, hardening hair, elasticity, suppleness and lubricity. The degree was evaluated according to the following criteria by professional panelists in four levels.
◎:対照と比較して明らかに有意な差異が認められる。⊚: Clearly significant difference is recognized as compared with the control.
○:対照と比較て有意な差異が認められる。◯: A significant difference is recognized as compared with the control.
△:対照と比較して少し有意な差異が認められる。Δ: A little significant difference is recognized as compared with the control.
×:対照と比較して有意な差異が認められない。X: No significant difference is recognized compared to the control.
さらに実用性および総合評価について意以下の基準に従
って評価した。Furthermore, practicality and overall evaluation were evaluated according to the following criteria.
実用性 ◎:洗髪後も効果に変化がなく、充分実用性があると考
えられる。Practicality ⊚: The effect does not change even after washing the hair, and is considered to be sufficiently practical.
○:選択後若干効果が消失するが、実用性があると考え
られる。◯: The effect disappears slightly after selection, but it is considered to be practical.
×:洗髪後効果が消失するか、その他、臭い等不都合な
性質を有し実用性がない。X: The effect disappears after washing hair, or it has other inconvenient properties such as odor and is not practical.
総合評価 ◎:すぐれた毛髪改質効果があり、実用性がある。Comprehensive evaluation ⊚: It has an excellent hair modifying effect and is practical.
○:毛髪改質効果があり、実用性がある。◯: It has a hair-modifying effect and is practical.
×:毛髪改質効果が期待できないか、その他臭い等実用
上不都合な性質を有する。X: A hair-modifying effect cannot be expected, or it has other practically inconvenient properties such as odor.
表3から明らかなようにアルデヒド類を組成物全量に対
して0.5〜20重量%配合した場合実用性のある毛髪改質
剤組成物が得られる。また、配合するアルデヒドの種類
によって毛質が軟化するものと硬化するものがあり、例
えば、バニリンまたはアルキルアルデヒド類配合組成物
は毛質軟化作用を示し、一方、シンナムアルデヒド類配
合組成物は毛質硬化作用を示すことがわかる。 As is clear from Table 3, when the aldehydes are blended in an amount of 0.5 to 20% by weight based on the total amount of the composition, a practical hair modifier composition can be obtained. Further, depending on the type of aldehyde to be blended, there are those that soften the hair and those that harden.For example, a vanillin or alkyl aldehyde compounding composition exhibits a hair softening action, while a cinnamaldehyde compounding composition It can be seen that it exhibits a curing action.
実施例18 成分 重量% バニリン 3.00 自己乳化型モノステアリン酸グリセリン 3.00 セタノール 1.00 オレイルアルコール 2.00 流動パラフィン 8.00 カルボキシビニルポリマー 0.25 香料 適量 水酸化カリウム(1%水溶液) 12.5 イオン交換水 100に調整 自己乳化型モノステアリン酸グリセリン、セタノール、
オレイルアルコール、流動パラフィンの混合物を80℃に
溶解し、これにカルボキシビニルポリマーおよびイオン
交換水の混合物を80℃に加温して加え、2000回転/分の
高速回転強剪断を5分行なった。その後、冷却し、40℃
で香料、38℃でバニリン(20%水溶液に調整)を加え、
充分撹拌して乳液状毛髪改質剤組成物を得た。Example 18 Ingredients% by weight vanillin 3.00 self-emulsifying glyceryl monostearate 3.00 cetanol 1.00 oleyl alcohol 2.00 liquid paraffin 8.00 carboxyvinyl polymer 0.25 perfume proper amount potassium hydroxide (1% aqueous solution) 12.5 self-emulsifying monostearin Glycerin acid, cetanol,
A mixture of oleyl alcohol and liquid paraffin was dissolved at 80 ° C., a mixture of carboxyvinyl polymer and ion-exchanged water was heated to 80 ° C., and the mixture was subjected to 2000 rpm / min high speed strong shearing for 5 minutes. Then, cool down to 40 ℃
Add flavor and vanillin (adjusted to 20% aqueous solution) at 38 ℃,
After sufficiently stirring, a milky liquid hair modifier composition was obtained.
実施例19 成分 重量% ドテシルアルデヒド 3.00 ポリオキシエチレン硬化ヒマシ油 0.30 プロピレングリコール 5.00 蛋白質加水分解物 0.05 95%エチルアルコール 50.00 香料 適量 イオン交換水 100に調整 香料をポリオキシエチレン硬化ヒマシ油に溶解し、つい
でイオン交換水を加え、撹拌しながらプロピレングリコ
ール、蛋白質加水分解物およびドデシルアルコールの95
%エタノール溶液を順次加えてローション状毛髪改質剤
組成物を得た。Example 19 Ingredients wt% Dotesyl aldehyde 3.00 Polyoxyethylene hydrogenated castor oil 0.30 Propylene glycol 5.00 Protein hydrolyzate 0.05 95% Ethyl alcohol 50.00 Fragrance Suitable amount Ion-exchanged water 100 Dissolved perfume in polyoxyethylene hydrogenated castor oil, Next, ion-exchanged water was added, and propylene glycol, protein hydrolyzate and dodecyl alcohol 95% were added with stirring.
% Ethanol solution was sequentially added to obtain a lotion-shaped hair modifier composition.
実施例20 ステアリン酸、セタノール、モノステアリン酸ポリエチ
レングリコール(23E.O.)、ジ‐2-エチルヘキサン酸ネ
オペンチルグリコール、ミツロウ、モノピログルタミン
酸モノイソステアリン酸硬化ヒマシ油の混合液を80℃で
溶解し、これにポリビニルピロリドン、グリセリン、ポ
リエチレングリコール(300E.O.)、アシルグルタミン
ソーダ、トリエタノールアミン、イオン交換水の溶液を
80℃で加え、2000回転/分の高速回転強剪断を5分行な
った。その後冷却して40℃で香料とシンナムアルデヒド
を加え、充分撹拌した。得られた乳液およびフロン12ガ
スを適量容器に充填してムース状毛髪改質組成物を得
た。Example 20 Stearic acid, cetanol, polyethylene glycol monostearate (23E.O.), neopentyl glycol di-2-ethylhexanoate, beeswax, monoisoglutearate monoisostearate A mixture of hydrogenated castor oil is dissolved at 80 ° C. A solution of polyvinylpyrrolidone, glycerin, polyethylene glycol (300E.O.), acylglutamine soda, triethanolamine, and ion-exchanged water.
The mixture was added at 80 ° C., and 2000 rpm / minute high-speed rotation strong shearing was performed for 5 minutes. After cooling, the fragrance and cinnamaldehyde were added at 40 ° C., and the mixture was thoroughly stirred. An appropriate amount of the obtained emulsion and Freon 12 gas was filled in a container to obtain a mousse-shaped hair modifying composition.
Claims (1)
デヒド、シンナムアルデヒド誘導体、炭素数8〜22のア
ルキルアルデヒドおよびこれらの2種以上の混合物から
なる群から選ばれる化合物0.5〜20重量%を含有するこ
とを特徴とする毛髪を硬毛化または軟毛化するための毛
髪改善剤組成物。1. An active ingredient containing 0.5 to 20% by weight of a compound selected from the group consisting of vanillin, cinnamaldehyde, cinnamaldehyde derivatives, alkyl aldehydes having 8 to 22 carbon atoms, and mixtures of two or more thereof. A hair improving composition for hardening or softening hair.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP61206589A JPH0667820B2 (en) | 1986-09-01 | 1986-09-01 | Hair modifier composition |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP61206589A JPH0667820B2 (en) | 1986-09-01 | 1986-09-01 | Hair modifier composition |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS6360916A JPS6360916A (en) | 1988-03-17 |
JPH0667820B2 true JPH0667820B2 (en) | 1994-08-31 |
Family
ID=16525905
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP61206589A Expired - Fee Related JPH0667820B2 (en) | 1986-09-01 | 1986-09-01 | Hair modifier composition |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0667820B2 (en) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE19757508A1 (en) * | 1997-12-23 | 1999-06-24 | Henkel Kgaa | Compositions for enhancing hair shine |
-
1986
- 1986-09-01 JP JP61206589A patent/JPH0667820B2/en not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
---|---|
JPS6360916A (en) | 1988-03-17 |
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