JPS58162513A - Hair permanent treating agent - Google Patents
Hair permanent treating agentInfo
- Publication number
- JPS58162513A JPS58162513A JP58008612A JP861283A JPS58162513A JP S58162513 A JPS58162513 A JP S58162513A JP 58008612 A JP58008612 A JP 58008612A JP 861283 A JP861283 A JP 861283A JP S58162513 A JPS58162513 A JP S58162513A
- Authority
- JP
- Japan
- Prior art keywords
- hair
- general formula
- weight
- integer
- agent
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 239000003795 chemical substances by application Substances 0.000 claims description 39
- ROSDSFDQCJNGOL-UHFFFAOYSA-N Dimethylamine Chemical compound CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 claims description 12
- KWIUHFFTVRNATP-UHFFFAOYSA-N Betaine Natural products C[N+](C)(C)CC([O-])=O KWIUHFFTVRNATP-UHFFFAOYSA-N 0.000 claims description 11
- 150000001875 compounds Chemical class 0.000 claims description 10
- 229920002125 Sokalan® Polymers 0.000 claims description 7
- 238000000034 method Methods 0.000 claims description 7
- 229960003237 betaine Drugs 0.000 claims description 6
- 239000001913 cellulose Substances 0.000 claims description 6
- 229920002678 cellulose Polymers 0.000 claims description 6
- 150000004665 fatty acids Chemical class 0.000 claims description 6
- 125000004432 carbon atom Chemical group C* 0.000 claims description 5
- 229910052739 hydrogen Inorganic materials 0.000 claims description 5
- 230000009467 reduction Effects 0.000 claims description 5
- 239000002280 amphoteric surfactant Substances 0.000 claims description 4
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 4
- 239000000194 fatty acid Substances 0.000 claims description 4
- 229930195729 fatty acid Natural products 0.000 claims description 4
- 230000003647 oxidation Effects 0.000 claims description 4
- 238000007254 oxidation reaction Methods 0.000 claims description 4
- 239000004584 polyacrylic acid Substances 0.000 claims description 4
- 230000008569 process Effects 0.000 claims description 4
- 229910052708 sodium Inorganic materials 0.000 claims description 4
- 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 claims description 3
- 229920002134 Carboxymethyl cellulose Polymers 0.000 claims description 3
- 239000000783 alginic acid Substances 0.000 claims description 3
- 235000010443 alginic acid Nutrition 0.000 claims description 3
- 229920000615 alginic acid Polymers 0.000 claims description 3
- 229960001126 alginic acid Drugs 0.000 claims description 3
- 150000004781 alginic acids Chemical class 0.000 claims description 3
- 239000001768 carboxy methyl cellulose Substances 0.000 claims description 3
- 235000010948 carboxy methyl cellulose Nutrition 0.000 claims description 3
- 239000008112 carboxymethyl-cellulose Substances 0.000 claims description 3
- 125000002091 cationic group Chemical group 0.000 claims description 3
- 229920003086 cellulose ether Polymers 0.000 claims description 3
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 claims description 2
- 229920002845 Poly(methacrylic acid) Polymers 0.000 claims description 2
- 229910052799 carbon Inorganic materials 0.000 claims description 2
- 125000001183 hydrocarbyl group Chemical group 0.000 claims description 2
- TWNIBLMWSKIRAT-VFUOTHLCSA-N levoglucosan Chemical group O[C@@H]1[C@@H](O)[C@H](O)[C@H]2CO[C@@H]1O2 TWNIBLMWSKIRAT-VFUOTHLCSA-N 0.000 claims description 2
- LGRLWUINFJPLSH-UHFFFAOYSA-N methanide Chemical compound [CH3-] LGRLWUINFJPLSH-UHFFFAOYSA-N 0.000 claims description 2
- 235000003441 saturated fatty acids Nutrition 0.000 claims description 2
- 150000004671 saturated fatty acids Chemical class 0.000 claims description 2
- 229940079593 drug Drugs 0.000 claims 3
- 239000003814 drug Substances 0.000 claims 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 1
- KWIUHFFTVRNATP-UHFFFAOYSA-O N,N,N-trimethylglycinium Chemical compound C[N+](C)(C)CC(O)=O KWIUHFFTVRNATP-UHFFFAOYSA-O 0.000 claims 1
- 239000001257 hydrogen Substances 0.000 claims 1
- 239000000834 fixative Substances 0.000 description 11
- 239000007800 oxidant agent Substances 0.000 description 9
- 239000000243 solution Substances 0.000 description 9
- 238000011282 treatment Methods 0.000 description 9
- 239000002253 acid Substances 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- ATRRKUHOCOJYRX-UHFFFAOYSA-N Ammonium bicarbonate Chemical compound [NH4+].OC([O-])=O ATRRKUHOCOJYRX-UHFFFAOYSA-N 0.000 description 5
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 5
- 239000001099 ammonium carbonate Substances 0.000 description 5
- 235000019864 coconut oil Nutrition 0.000 description 5
- 239000003240 coconut oil Substances 0.000 description 5
- 230000008719 thickening Effects 0.000 description 5
- PMNLUUOXGOOLSP-UHFFFAOYSA-N 2-mercaptopropanoic acid Chemical compound CC(S)C(O)=O PMNLUUOXGOOLSP-UHFFFAOYSA-N 0.000 description 4
- 239000000654 additive Substances 0.000 description 4
- 108010076876 Keratins Proteins 0.000 description 3
- 102000011782 Keratins Human genes 0.000 description 3
- 230000002378 acidificating effect Effects 0.000 description 3
- 235000012501 ammonium carbonate Nutrition 0.000 description 3
- 239000007864 aqueous solution Substances 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- -1 mercapto compounds Chemical class 0.000 description 3
- 239000003921 oil Substances 0.000 description 3
- 235000019198 oils Nutrition 0.000 description 3
- 239000002304 perfume Substances 0.000 description 3
- 239000011734 sodium Substances 0.000 description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- 229910000013 Ammonium bicarbonate Inorganic materials 0.000 description 2
- 235000013162 Cocos nucifera Nutrition 0.000 description 2
- 244000060011 Cocos nucifera Species 0.000 description 2
- PQUCIEFHOVEZAU-UHFFFAOYSA-N Diammonium sulfite Chemical compound [NH4+].[NH4+].[O-]S([O-])=O PQUCIEFHOVEZAU-UHFFFAOYSA-N 0.000 description 2
- BWGNESOTFCXPMA-UHFFFAOYSA-N Dihydrogen disulfide Chemical compound SS BWGNESOTFCXPMA-UHFFFAOYSA-N 0.000 description 2
- 108010010803 Gelatin Proteins 0.000 description 2
- 230000009471 action Effects 0.000 description 2
- 150000001447 alkali salts Chemical class 0.000 description 2
- 235000012538 ammonium bicarbonate Nutrition 0.000 description 2
- ZZTCCAPMZLDHFM-UHFFFAOYSA-N ammonium thioglycolate Chemical compound [NH4+].[O-]C(=O)CS ZZTCCAPMZLDHFM-UHFFFAOYSA-N 0.000 description 2
- 229940075861 ammonium thioglycolate Drugs 0.000 description 2
- SXDBWCPKPHAZSM-UHFFFAOYSA-M bromate Inorganic materials [O-]Br(=O)=O SXDBWCPKPHAZSM-UHFFFAOYSA-M 0.000 description 2
- SXDBWCPKPHAZSM-UHFFFAOYSA-N bromic acid Chemical compound OBr(=O)=O SXDBWCPKPHAZSM-UHFFFAOYSA-N 0.000 description 2
- 239000003638 chemical reducing agent Substances 0.000 description 2
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 2
- 239000012530 fluid Substances 0.000 description 2
- 229920000159 gelatin Polymers 0.000 description 2
- 239000008273 gelatin Substances 0.000 description 2
- 235000019322 gelatine Nutrition 0.000 description 2
- 235000011852 gelatine desserts Nutrition 0.000 description 2
- 230000007935 neutral effect Effects 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 238000003672 processing method Methods 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 230000037380 skin damage Effects 0.000 description 2
- XUXNAKZDHHEHPC-UHFFFAOYSA-M sodium bromate Chemical compound [Na+].[O-]Br(=O)=O XUXNAKZDHHEHPC-UHFFFAOYSA-M 0.000 description 2
- GEHJYWRUCIMESM-UHFFFAOYSA-L sodium sulfite Chemical compound [Na+].[Na+].[O-]S([O-])=O GEHJYWRUCIMESM-UHFFFAOYSA-L 0.000 description 2
- CWERGRDVMFNCDR-UHFFFAOYSA-N thioglycolic acid Chemical compound OC(=O)CS CWERGRDVMFNCDR-UHFFFAOYSA-N 0.000 description 2
- 238000004804 winding Methods 0.000 description 2
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 1
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 1
- TWJNQYPJQDRXPH-UHFFFAOYSA-N 2-cyanobenzohydrazide Chemical compound NNC(=O)C1=CC=CC=C1C#N TWJNQYPJQDRXPH-UHFFFAOYSA-N 0.000 description 1
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 1
- XWNSFEAWWGGSKJ-UHFFFAOYSA-N 4-acetyl-4-methylheptanedinitrile Chemical compound N#CCCC(C)(C(=O)C)CCC#N XWNSFEAWWGGSKJ-UHFFFAOYSA-N 0.000 description 1
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 1
- XUJNEKJLAYXESH-REOHCLBHSA-N L-Cysteine Chemical compound SC[C@H](N)C(O)=O XUJNEKJLAYXESH-REOHCLBHSA-N 0.000 description 1
- 239000005639 Lauric acid Substances 0.000 description 1
- 235000021360 Myristic acid Nutrition 0.000 description 1
- TUNFSRHWOTWDNC-UHFFFAOYSA-N Myristic acid Natural products CCCCCCCCCCCCCC(O)=O TUNFSRHWOTWDNC-UHFFFAOYSA-N 0.000 description 1
- 239000005642 Oleic acid Substances 0.000 description 1
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 1
- 239000004153 Potassium bromate Substances 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical class OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 150000003863 ammonium salts Chemical class 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 229920006318 anionic polymer Polymers 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 229920006317 cationic polymer Polymers 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 230000003750 conditioning effect Effects 0.000 description 1
- XUJNEKJLAYXESH-UHFFFAOYSA-N cysteine Natural products SCC(N)C(O)=O XUJNEKJLAYXESH-UHFFFAOYSA-N 0.000 description 1
- 235000018417 cysteine Nutrition 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- SUPCQIBBMFXVTL-UHFFFAOYSA-N ethyl 2-methylprop-2-enoate Chemical compound CCOC(=O)C(C)=C SUPCQIBBMFXVTL-UHFFFAOYSA-N 0.000 description 1
- UUFFXMPIDQJWET-UHFFFAOYSA-N ethyl 2-methylprop-2-enoate;hydrochloride Chemical compound Cl.CCOC(=O)C(C)=C UUFFXMPIDQJWET-UHFFFAOYSA-N 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
- 230000003472 neutralizing effect Effects 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
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- BOWVQLFMWHZBEF-KTKRTIGZSA-N oleoyl ethanolamide Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)NCCO BOWVQLFMWHZBEF-KTKRTIGZSA-N 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 230000035699 permeability Effects 0.000 description 1
- 229920000193 polymethacrylate Polymers 0.000 description 1
- 229940094037 potassium bromate Drugs 0.000 description 1
- 235000019396 potassium bromate Nutrition 0.000 description 1
- 238000005956 quaternization reaction Methods 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 210000004761 scalp Anatomy 0.000 description 1
- 229960001922 sodium perborate Drugs 0.000 description 1
- 235000010265 sodium sulphite Nutrition 0.000 description 1
- YKLJGMBLPUQQOI-UHFFFAOYSA-M sodium;oxidooxy(oxo)borane Chemical compound [Na+].[O-]OB=O YKLJGMBLPUQQOI-UHFFFAOYSA-M 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-L sulfite Chemical class [O-]S([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-L 0.000 description 1
- 230000008961 swelling Effects 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 150000004670 unsaturated fatty acids Chemical class 0.000 description 1
- 235000021122 unsaturated fatty acids Nutrition 0.000 description 1
- AQLJVWUFPCUVLO-UHFFFAOYSA-N urea hydrogen peroxide Chemical compound OO.NC(N)=O AQLJVWUFPCUVLO-UHFFFAOYSA-N 0.000 description 1
- 239000000341 volatile oil Substances 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 239000000080 wetting agent Substances 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
- A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
- A61K8/81—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
- A61K8/8141—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
- A61K8/8147—Homopolymers or copolymers of acids; Metal or ammonium salts thereof, e.g. crotonic acid, (meth)acrylic acid; Compositions of derivatives of such polymers
-
- 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
- A61K8/40—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
- A61K8/42—Amides
-
- 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
- A61K8/40—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
- A61K8/44—Aminocarboxylic acids or derivatives thereof, e.g. aminocarboxylic acids containing sulfur; Salts; Esters or N-acylated derivatives thereof
- A61K8/442—Aminocarboxylic acids or derivatives thereof, e.g. aminocarboxylic acids containing sulfur; Salts; Esters or N-acylated derivatives thereof substituted by amido group(s)
-
- 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
- A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
- A61K8/73—Polysaccharides
- A61K8/731—Cellulose; Quaternized cellulose derivatives
-
- 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
- A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
- A61K8/81—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
- A61K8/8141—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
- A61K8/8152—Homopolymers or copolymers of esters, e.g. (meth)acrylic acid esters; Compositions of derivatives of such polymers
-
- 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
- A61Q5/04—Preparations for permanent waving or straightening the hair
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
- A61K2800/40—Chemical, physico-chemical or functional or structural properties of particular ingredients
- A61K2800/54—Polymers characterized by specific structures/properties
- A61K2800/542—Polymers characterized by specific structures/properties characterized by the charge
- A61K2800/5422—Polymers characterized by specific structures/properties characterized by the charge nonionic
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
- A61K2800/40—Chemical, physico-chemical or functional or structural properties of particular ingredients
- A61K2800/54—Polymers characterized by specific structures/properties
- A61K2800/542—Polymers characterized by specific structures/properties characterized by the charge
- A61K2800/5424—Polymers characterized by specific structures/properties characterized by the charge anionic
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
- A61K2800/40—Chemical, physico-chemical or functional or structural properties of particular ingredients
- A61K2800/54—Polymers characterized by specific structures/properties
- A61K2800/542—Polymers characterized by specific structures/properties characterized by the charge
- A61K2800/5426—Polymers characterized by specific structures/properties characterized by the charge cationic
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Birds (AREA)
- Epidemiology (AREA)
- Cosmetics (AREA)
Abstract
(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。(57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.
Description
【発明の詳細な説明】
本発明は毛髪のパーマネント加工における還元ないしは
酸化工程用の薬剤に関する。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to agents for reduction or oxidation steps in the permanent processing of hair.
通常の上転のパーマネント加工にお込ては、毛髪はまず
還元性化合物、特にメルカプト化合物、の水性液で、な
かでもアルカリ性系におけるチオグリコレートあるいは
弱酸性ないしは中性系における亜硫酸塩で、処理される
。これによって毛髪ケラチンのジサルファイド架橋が化
学反応によって切断され、毛髪が簡単にパーマネント加
工される様にな、る。In conventional permanent hair treatments, hair is first treated with an aqueous solution of reducing compounds, especially mercapto compounds, especially thioglycolates in alkaline systems or sulfites in weakly acidic or neutral systems. be done. This breaks the disulfide crosslinks in hair keratin through a chemical reaction, allowing the hair to be easily permanentized.
実際に人の髪をパーマネント加工する場合は一般に二つ
の方法がとられる。第一の方法では、まず毛髪を洗浄し
、タオルで水分をぬぐい去った後、いくつかの束に分け
、これらの束をそれぞれパーマネント加工剤液の一部を
用いて湿らせ、カーラーに巻き上げる。巻き上げ終了後
、巻いた状態で毛髪を残りのパーマネント加工剤液で湿
らせる。第二の方法においては、毛髪はまず同様に洗浄
し、タオルで水分をぬぐい去つた後、いくつかの束に分
けるが、次にあらかじめパーマネント加工剤液で湿らせ
ることをしないで、カーラーに巻き上げる。そして巻き
上げ終了後にパーマネント加工剤液の必要量全量を巻き
上げた毛髪に付与する。ところでこれらの場合にパーマ
ネントウェーブ加工には約5ないし13ミリメーターの
直径のカーラーが使用され、ウェーブ除去加工には13
ミリメ一ター以上の直径を有するカーラーが使用される
。There are generally two methods used to permanently process human hair. In the first method, the hair is first washed and dried with a towel, then divided into several strands, each of which is moistened with a portion of the permanent solution and wound into curlers. After winding, moisten the hair with the remaining permanent treatment solution. In the second method, the hair is first similarly washed, dried with a towel, and then divided into several bundles, but then wound into curlers without being pre-moistened with a permanent solution. . After the winding is completed, the entire required amount of permanent finishing agent liquid is applied to the hair. By the way, in these cases, a curler with a diameter of about 5 to 13 mm is used for permanent waving, and a curler with a diameter of about 13 mm is used for wave removal.
Curlers with a diameter of a millimeter or more are used.
パーマネント加工剤の毛髪に対する作用時聞け、パーマ
ネントウェーブ加工の場合もウェーブ除去加工の場合も
同様に、毛髪の性状および所望とする加工の度合に応じ
て選択されるが、一般には30分程度である。加熱する
ことによって、例えば熱放射器やフードドライヤーを用
いることによって、作用時聞を短縮することができる。The action of the permanent processing agent on the hair is selected depending on the properties of the hair and the desired degree of processing, but it is generally about 30 minutes for both permanent wave processing and wave removal processing. . By heating, for example by using a heat radiator or a food dryer, the working time can be shortened.
パーマネント加工剤を所定の時間作用させた後、カーラ
ーに巻いたまま毛髪を十分水洗する。After allowing the permanent finishing agent to act for a predetermined period of time, the hair is thoroughly washed with water while still wrapped in curlers.
第二段階において毛髪を酸化剤、望ましくは臭素酸塩溶
液あるいは過酸化水素溶液、で処理して形状固定を行な
う。これによって先に切断された毛髪ケラチンのジサル
ファイド架橋が新しい形状において再結合される。毛髪
に対する固定剤の作用時間は一般には約10ないし15
分である。In a second step, the hair is treated with an oxidizing agent, preferably a bromate solution or a hydrogen peroxide solution, to achieve shape fixation. This causes the disulfide crosslinks of the hair keratin that were previously cut to be recombined in a new form. The action time of the fixative on the hair is generally about 10 to 15
It's a minute.
次にカーラーをはずした後毛髪を十分水で洗浄する。Next, remove the curlers and wash your hair thoroughly with water.
しかしながら上に述べた毛髪のパーマネント加工法の場
合、パーマネント加工剤液並びに固定剤液による作業に
は多大な難点がある。特に十分注意して作業を行なって
も、加工液が頭皮や理容師の手に付着するのは避は難く
、従って皮膚障害が生じるなどの問題がある。その他パ
ーマネント加工液ないしは固定液が毛髪から流れ落ちて
しまって、加工目的を達成し得ない場合もある。However, in the case of the above-mentioned permanent hair processing method, there are many difficulties in working with a permanent processing agent solution and a fixative solution. Even if the work is carried out with particular care, it is difficult to avoid the processing liquid from adhering to the scalp or hands of the barber, resulting in problems such as skin damage. In other cases, the permanent processing solution or fixative solution may run down from the hair, making it impossible to achieve the processing objective.
そこでパーマネント加工剤および固定剤を増粘し、ゲル
状ないしはクリーム状にしようという試みがなされてい
る。Therefore, attempts have been made to thicken permanent finishing agents and fixatives to make them gel-like or cream-like.
しかし今までのところ種々の理由から、増粘したパーマ
ネント加工剤ないしは固定剤を実際に使用するという段
階には至っていない。特にこれらの調合剤は増粘剤を含
有するため、巻き上げだ毛髪の内部には十分浸透しえな
hうらみがあり、さらに上に述べたパーマネント加工法
の場合かえって操作がむつかしくなる。すなわち今まで
に提供されてしる増粘パーマネント加工剤を使用した場
合毛髪のすべりがよくなるために、これを付与した毛髪
はカーラーに巻きすらい。However, for various reasons, we have not yet reached the stage where thickened permanent finishing agents or fixatives are actually used. In particular, since these preparations contain thickeners, they cannot penetrate into the inside of curly hair sufficiently, and furthermore, in the case of the above-mentioned permanent processing method, the operation is rather difficult. That is, when the thickening permanent finishing agents that have been provided so far are used, the hair becomes smoother, so that the hair coated with this agent can be wound in curlers.
その他に、今までに提供されている増粘パーマネント加
工剤ないしは固定剤のほとんどが、洗浄しても毛髪から
なかなか落ちないという欠点を持っている。In addition, most of the thickening permanent finishing agents or fixatives that have been provided so far have the disadvantage that they are difficult to remove from the hair even after washing.
さらに、たとえば増粘添加物としてゼラチンを含有する
ような、アルカリ性増粘パーマネント加工剤は貯蔵安定
性が劣る。その上ゼラチンの添加によって加工剤の加工
能力は減少する。Furthermore, alkaline thickening permanent finishing agents, such as those containing gelatin as a thickening additive, have poor storage stability. Moreover, the addition of gelatin reduces the processing capacity of the processing agent.
ところがここに、A)(1)カチオン活性セルロースお
よび/あるいはポリトリメチルアンモニウムメチルメタ
クリレート、あるいは(1)ポリアクリル酸、ポリメタ
クリル酸、カルボキシメチルセルロースおよび/あるい
はアルギン酸、を0.工ないし1.5重量%、B)炭素
原子を12ないし18個含有する一個以上の飽和および
/あるいは不飽和脂肪酸のエタノールアミドおよび/あ
るいはイソプロパツールアミド−個以上を0.1ないし
3.0重量%−C)下記一般式(1)あるいは(II)
であられされる両性界面活性剤−個以」二を0.05な
いし0.8重量%、およびD)脂肪酸残基中の炭素原子
数が12ないし18個である脂肪酸ジメチルアンモニウ
ムベタインを0.05ないし1.5重量%、組合せて含
有することを特徴とする還元ないしは酸化工程用のパー
マネント加工液は上に述べた様な欠点を示すことなく、
簡単に増粘パーマネント加工液を提供し得ることが、見
い出された。However, here, A) (1) cationically activated cellulose and/or polytrimethylammonium methyl methacrylate, or (1) polyacrylic acid, polymethacrylic acid, carboxymethylcellulose and/or alginic acid, is added to 0. B) 0.1 to 3.0 ethanolamides and/or isopropanolamides of one or more saturated and/or unsaturated fatty acids containing 12 to 18 carbon atoms; Weight%-C) The following general formula (1) or (II)
D) 0.05 to 0.8% by weight of an amphoteric surfactant comprised of D) 0.05 to 0.8% by weight of dimethylammonium betaine, a fatty acid having 12 to 18 carbon atoms in the fatty acid residue; Permanent processing fluids for reduction or oxidation processes, characterized in that they contain 1.5% to 1.5% by weight in combination, do not exhibit the above-mentioned drawbacks,
It has been found that it is possible to easily provide a thickened permanent processing fluid.
RΦ
1
R3−C−NH−CH2−CH2−N−C)R2−CO
OA (i+)2
〔ここでR1はCH2−CH2−OH,CH2−CH2
−CUOA(A−H+ Na ) * R2はC12−
C00A、 CH2−CH2−C00A、CH2−C
H2−0−CH2−COOA、CH□−Ct12−OC
H2CH2C00A (A−H、Na )、さらにR3
は炭素原子数7ないし18の直鎖炭化水素残基、望まし
くはC7H15,C3H19,C11H23,あるいは
C1□H35をあられす。〕
本発明による加工剤中に含有される、成分Aとしてあら
れされている高分子化合物は、カチオン活性セルロース
およびポリトリメチルアンモニウムエチルメタクリレー
トのように、カチオン性を示すか、あるいはポリアクリ
ル酸、ポリメタクリル酸、カルボキシメチルセルロース
およびアルギン酸のように、アニオン性を示す。RΦ 1 R3-C-NH-CH2-CH2-N-C) R2-CO
OA (i+)2 [Here, R1 is CH2-CH2-OH, CH2-CH2
-CUOA(A-H+ Na) *R2 is C12-
C00A, CH2-CH2-C00A, CH2-C
H2-0-CH2-COOA, CH□-Ct12-OC
H2CH2C00A (A-H, Na), further R3
represents a straight chain hydrocarbon residue having 7 to 18 carbon atoms, preferably C7H15, C3H19, C11H23, or C1□H35. ] The polymer compound contained in the processing agent according to the present invention and shown as component A is cationic, such as cationically activated cellulose and polytrimethylammonium ethyl methacrylate, or polyacrylic acid, polymethacrylate, etc. Acids, like carboxymethylcellulose and alginic acid, exhibit anionic properties.
しかし加工剤はカチオン性高分子化合物だけ、あるbは
アニオン性高分子化合物だけを含有しなければならない
というわけではなく、上に挙げたカチオン性高分子化合
物およびアニオン性高分子化合物はいずれも適宜組合せ
て使用することができる。However, the processing agent does not necessarily have to contain only cationic polymer compounds, or only anionic polymer compounds. Can be used in combination.
カチオン活性セルロースとしてハ、特許下記一般式であ
られされる、米国特許明細書第3472840号に記載
の、カチオン性セルロースエーテルが望ましい。As the cationically activated cellulose, cationic cellulose ethers described in US Pat. No. 3,472,840, which are represented by the following general formula, are desirable.
〔ここでRcellはアンヒドログルコース単位、Yは
50ないし20000の整数、さらにRは個別に丁記一
般式であられされる置換基をあられす。[Here, Rcell is an anhydroglucose unit, Y is an integer from 50 to 20,000, and R is an individual substituent represented by the general formula shown above.
OH3
(ここでmはOないし10の整数、nは0ないし3の整
数、さらにpは1ないし10の整数をあられす。)〕
上記一般式であられされるセルロースエーテルの内、特
に適するものとしてユニオン・カーバイド社製の、ポリ
マーJR400という商品名で知られている製品を挙げ
ることができる。OH3 (where m is an integer of O to 10, n is an integer of 0 to 3, and p is an integer of 1 to 10)] Among the cellulose ethers represented by the above general formula, particularly suitable are Mention may be made of the product manufactured by Union Carbide and known under the trade name Polymer JR400.
一般式(CH2=CH−COOH)nであられされるポ
リアクリル酸のうち、本発明において使用することがで
きるものとして、たとえばB、F、グツドリッチ ケミ
カル社製の、カルボポールという商品名で市販されてb
る製品を挙げることができる。Among the polyacrylic acids having the general formula (CH2=CH-COOH)n, examples of polyacrylic acids that can be used in the present invention include B, F, which is commercially available under the trade name Carbopol manufactured by Gudrich Chemical Co. Teb
The following products can be mentioned.
本発明による加工剤中に含有される脂肪酸エタノールア
ミドないしはイソプロパツールアミドとしては、特にオ
レイン酸エタノールアミド。Fatty acid ethanolamide or isopropanolamide contained in the processing agent according to the invention is in particular oleic acid ethanolamide.
ヤシ油酸ジェタノールアミド、ヤシ油酸七ノエタノール
アミド、ラウリン酸ジイソプロパツールアミド、ミリス
チン酸ジェタノールアミド。Coco acid jetanolamide, coconut oil heptanoethanolamide, lauric acid diisopropanolamide, myristic acid jetanolamide.
ステアリン酸ジェタノールアミド、およびヤシ油酸ポリ
ジェタノールアミドが望ましい。Stearic acid jetanolamide and coconut acid polyjetanolamide are preferred.
両性界面活性剤としては、たとえば下記一般式であられ
される化合物が適当である。As the amphoteric surfactant, for example, a compound represented by the following general formula is suitable.
\
CH2−CH2−OH
その餞これに属する化合物としてミラノール・ケミカル
社製の、ミラノールという商品名で市販されている製品
が望ましい。これらの製品の代表的なものは下記一般式
であられされる化合物である。\CH2-CH2-OH As a compound belonging to this category, a product commercially available under the trade name Milanol manufactured by Milanol Chemical Company is desirable. Representative of these products are compounds represented by the following general formula.
OCH2C00A
ココヤシ−C−NH−CH2−CH2−N−CH2CH
20HCH2C00A
(A=H、Na ) (商品名:ミラ/ −/l/ C
2M )適当な脂肪酸ジメチルアンモニウムベタインと
して、たとえばヤシ油酸ジメチルアンモニウムベタイン
を挙げることができる。OCH2C00A Coconut-C-NH-CH2-CH2-N-CH2CH
20HCH2C00A (A=H, Na) (Product name: Mira/-/l/C
2M) As a suitable fatty acid dimethylammonium betaine, mention may be made, for example, of dimethylammonium betaine coconut oil.
木兄明足よる毛髪の11(1T剤は還元性化合物として
、たとえばシスティン、チオグリコール酸。11 (1T agent) for hair according to Akari Kinoe contains reducing compounds such as cysteine and thioglycolic acid.
チオ乳酸、さらにこれらと無機な−しは有機塩法との塩
、さ、らにまた亜硫酸のアルカリ塩、特に亜硫酸アンモ
ニウム、を含有する。It contains thiolactic acid, salts thereof with inorganic or organic salts, and also alkali salts of sulfite, especially ammonium sulfite.
本発明による加工剤は、毛髪のケラチンを膨潤させる目
的で、たとえばイミダゾリジノン−(2)を含有し得る
。The processing agent according to the invention may contain, for example, imidazolidinone-(2) for the purpose of swelling the keratin of the hair.
本発明によるパーマネント加工剤は弱酸性ないし中性か
らアルカリ性の範囲内にPH調整される。特許、アンモ
ニヤ、モノエタノールアミン。The pH of the permanent finishing agent according to the present invention is adjusted within the range of weakly acidic to neutral to alkaline. Patent, ammonia, monoethanolamine.
炭酸アンモニウムおよび/あるいは炭酸水素アンモニウ
ムによって、5ないし10のPH値を示すように、調整
することが望ましい。It is desirable to adjust the pH value to 5 to 10 using ammonium carbonate and/or ammonium hydrogen carbonate.
ここに記載のパーマネント加工剤中に含有される還元性
化合物の量は、毛髪の加工において一般的に採用されて
いる量である。たとえばチオクリコール酸あるいはチオ
乳酸のアンモニウム塩の場合的2なLn(,12重量%
の濃度で含有される。酸性(例えばPH6,5ないし6
.9)に調整したパーマネント加工剤の場合は特に亜硫
酸ナトリウムするいは亜硫酸アンモニウム塩約3ないし
8重量%の濃度(so2として換算)において使用され
る。The amounts of reducing compounds contained in the permanent treatment agents described herein are those commonly employed in hair treatment. For example, in the case of ammonium salts of thiochlorocholic acid or thiolactic acid, Ln (12% by weight)
Contained at a concentration of Acidic (e.g. pH 6.5 to 6)
.. In the case of permanent finishing agents adjusted to 9), sodium sulfite or ammonium sulfite salts are used in particular at a concentration of about 3 to 8% by weight (calculated as SO2).
本発明による固定剤は酸化剤として特に過酸化水素ある
いは臭素酸のアルカリ塩を含有する。The fixative according to the invention contains as oxidizing agent, in particular hydrogen peroxide or an alkali salt of bromate.
酸化剤は、過剰のパーマネント加工剤を中和する働きと
、この調合剤によって柔軟化した毛髪を再び硬化させる
働きを、持っている。本発明において採用し得る酸化剤
は特定のものではなく、従来この目的に使用されている
酸化剤であれば適宜使用することができる。たとえば市
販の酸化剤の中から臭素酸カリウム、臭素酸ナトリウム
、過ホウ酸ナトリウム、過酸化水素。The oxidizing agent has the function of neutralizing excess permanent treatment agent and rehardening the hair that has been softened by this preparation. The oxidizing agent that can be employed in the present invention is not particularly limited, and any oxidizing agent that has been conventionally used for this purpose can be used as appropriate. For example, potassium bromate, sodium bromate, sodium perborate, and hydrogen peroxide among commercially available oxidizing agents.
および過酸化尿素を挙げることができる。酸化剤の濃度
は硬化条件、たとえば温度および時間、に応じて可変で
ある。通常固定剤中における酸化剤の濃度は約0.5な
いし10.0重量%である。and urea peroxide. The concentration of oxidizing agent is variable depending on the curing conditions, such as temperature and time. Usually the concentration of oxidizing agent in the fixative is about 0.5 to 10.0% by weight.
酸化剤は他の公知の添加剤と併用することができる。The oxidizing agent can be used in combination with other known additives.
本発明による加工剤が、たとえば毛髪コンディショニン
グ剤1毛髪保護剤、染料、香油などの、パーマネント加
工剤ないしは固定剤中に含有されている一般的な添加剤
を含有し得ることはもちろんである。これらの添加剤は
、実質的に加工剤の作用能力を損なわない範囲の量で、
使用される。It goes without saying that the treatment agents according to the invention may contain the usual additives contained in permanent treatment agents or fixatives, such as hair conditioning agents, hair protectants, dyes, perfume oils, and the like. These additives may be added in amounts that do not substantially impair the effectiveness of the processing agent.
used.
本発明による加工剤は水を60ないし95重量%含有し
、目的に応じて約5ないし100 m Pa 、s(ミ
リパスカル・秒)の粘度を有することが望ましい。The processing agent according to the present invention preferably contains 60 to 95% by weight of water and has a viscosity of about 5 to 100 mPa, s (milliPascal-second) depending on the purpose.
本発明による、毛髪のパーマネント加工における還元工
程ないしは酸化工程用の、水性パーマネント加工剤は、
巻き上げた毛髪の内部にも良好に浸透し、毛髪から流れ
落ちることがなく、しかも簡単に洗い流すことができる
。さらに本発明による、パーマネント加工における還元
工程用の加工剤を使用した場合、毛髪がすべり過ぎると
いうことがなくなる。さらにまた増粘成分人ないしDの
存在によって加工剤の加工能力が阻害されると−うこと
ももちろんなり0ところで本発明によるパーマネント加
工剤ないしは固定剤の特長は、成分A−Dを特定の重量
パーセント範囲内で使用して始めて、得られるものであ
る。たとえば成分Aを特定重量パーセント以上の濃度で
使用した場合、巻き上げた毛髪の内部への浸透度が確実
に低下する。成分Bを特定重量パーセント以上の濃度で
使用した場合、皮膚に障害を与える。成分CおよびDは
、′加工剤の粘度をいっそう高める働きを持っており、
その場合に同成分は相乗的に働き、成分Cあるいは成分
D゛単独は十分に効果を発揮し得ない。成分CおよびD
は上記の作用と同時に、湿潤剤としての働きも持ってお
り、これによって加工剤の浸透性が十分保障される。The aqueous permanent finishing agent for the reduction or oxidation process in the permanent finishing of hair according to the present invention comprises:
It penetrates well into the inside of curled hair, does not run off from the hair, and can be easily washed away. Furthermore, when using the treatment agent for the reduction step in permanent treatment according to the invention, the hair does not become too slippery. Furthermore, it goes without saying that the processing ability of the processing agent is inhibited by the presence of the thickening components A to D. However, the feature of the permanent processing agent or fixative according to the present invention is that the components A to D It can only be obtained by using within the percentage range. For example, if component A is used at a concentration above a certain weight percent, the degree of penetration into the inside of curled hair will definitely decrease. When component B is used in concentrations above a certain weight percent, it causes skin damage. Components C and D have the function of further increasing the viscosity of the processing agent,
In this case, the same components act synergistically, and component C or component D alone cannot exert sufficient effects. Components C and D
In addition to the above-mentioned functions, it also functions as a wetting agent, thereby ensuring sufficient permeability of the processing agent.
次に実施例によって本発明の対象をさらに詳しく説明す
る。Next, the object of the present invention will be explained in more detail by way of examples.
実施例1 還元剤含有パーマネント加工剤ポリアクリル
酸(カルボボーA/934°) 10.ogヤシ油
酸ジェタノールアミド 0.4g含
有するココヤシ油酸のアルキル残基
ヤシ油酸ジメチルアンモニウムベタイン ○、
フ9アンモニウムチオグリコレートの5o%水溶液 2
3.7g炭酸アンモニウム
3.0g炭酸水素アンモニウム
5.0g香油
0.2g水
65.6g100.0y
この粘着なパーマネント加工剤液のPH[は8.8であ
る。Example 1 Reducing agent-containing permanent finishing agent polyacrylic acid (Carbobo A/934°) 10. Alkyl residue of coconut oil containing 0.4 g of coconut oil jetanolamide Coco acid dimethylammonium betaine ○,
5o% aqueous solution of ammonium thioglycolate 2
3.7g ammonium carbonate
3.0g ammonium bicarbonate
5.0g perfume oil
0.2g water
65.6g100.0y The pH of this sticky permanent finishing agent solution is 8.8.
実施例2 還元剤含有パーマネント加工剤ポリトリメチ
ルアンモニウムエチルメタクリレートの塩酸塩(80%
四級化) 0.2gオレイン
酸ジェタノールアミド 。、1gアン
モニウムチオグリコレートの50%水溶液 19.5.
9炭酸アンモニウム
4.0g香油 。、IJ
水
75,29100.0.9
この粘着なパーマネント加工剤液のPH値は9.0であ
る。Example 2 Reducing agent-containing permanent finishing agent polytrimethylammonium ethyl methacrylate hydrochloride (80%
Quaternization) 0.2g oleic acid jetanolamide. , 1 g ammonium thioglycolate in 50% aqueous solution 19.5.
9 ammonium carbonate
4.0g fragrant oil. , I.J.
water
75,29100.0.9 The pH value of this sticky permanent finishing agent liquid is 9.0.
実施例3 固定剤 カチオン活性セルロース(ユニオンカーバイド社の 。Example 3 Fixative Cationically activated cellulose (Union Carbide).
ポ1−JR400’ ) 0
,2IIヤシ油酸ポリジエタノールアミド
(ヘンケル社のコンパランPD■) 0
.2.9ミラノール”C2M(一般式と記のとおり)
0.1.litヤシ油酸ジ酸ジメチルアンモニウ
ムベタイン 1.5g臭素酸ナトリウム
8.5g香油
。・IF7水
89.4p100.0.
9
上に述べたパーセント数はすべて重量パーセント数であ
る。Po1-JR400') 0
, 2II Coconut Acid Polydiethanolamide (Henkel Comparan PD■) 0
.. 2.9 Milanol”C2M (as shown in general formula)
0.1. lit dimethylammonium betaine coconut oil diacid 1.5g sodium bromate
8.5g perfume oil
.・IF7 water
89.4p100.0.
9 All percentages mentioned above are weight percentages.
特許出願人 ウエラ アクチェンゲゼルシャフト代
理人 新実健部 外1名Patent applicant Wella Akchengesellschaft agent Kenbu Shinji and 1 other person
Claims (1)
)カチオン活性セルロースおよび/あるいはポリトリメ
チルアンモニウムメチルメタクリレート、あるいは(1
)ポリアクリル酸、ポリメタクリル酸、カルボキシメチ
ルセルロースおよヒ/するいはアルギン酸、を0.1な
いし1.5重量%、B)炭素原子を12ないし18個含
有する一個以上の飽和および/あるいは不飽和脂肪酸の
エタノールアミドおよび/あるいはイソゾロパノールア
ミド−個以上を0.1ないし3.0重量%、C)下肥一
般式(1)あるいは(11)であられされる両性界面活
性剤−個以上を0.05ないし0.8重量%、およびL
))脂肪酸残基中の炭素原子数が12ないし18個であ
る脂肪酸ジメチルアン′モニウムベタインを0.05な
いし1.5重量%5組合せて含有することを特徴とする
還元工程ないしは酸化工程用薬剤。 2 〔ここでR3はCH2−CH2−OHあるいはCH2−
CI−(2−COOA(A−HlNa)、R2はCH2
−C00A 、 CH2−CH2−C00A 、 CH
2−CH2−0−CH2−COOAあるいはCH2CH
2OCH2CH2C00A (A−H、Na )、さら
にR3は炭素原子数7ないし18の直鎖炭化水素残基、
望ましくはC,R05,C9H,9,C,f−1□3
あるいはC1□H35をあられす。〕 (2) カチオン活性セルロースとして下記一般式で
あられされるカチオン性セルロースエーテルを含有する
ことを特徴とする特許請求の範囲の第1項に記載の薬剤
。 〔ここでRcellはアンヒドログルコース単位、Yは
50ないし20000の整数、さらにRは個別に下記一
般式であられされる基をあられす。 −(C2H40)m−(CH2CHO)n−(C2H4
0)、−HOH3 (ここでmは0ないし10の整数、nは○ないし3の整
数、さらにpはOないし1oの整数をあられす。)〕 (3)両性界面活性剤が下記一般式であられされる化合
物であることを特徴とする特許請求の範囲の第1項また
は第2項に記載の薬剤。 OCR’2COOA ココヤシ−〇−NH−CH,,−CH2−N−CH2−
CH2−OHCH2C00A (A=H、Na ) (4)約5な込しloomPa、s(ミリパスカル・秒
)の粘度を有することを特徴とする特許請求の範囲の第
1項〜第3項いずれかに記載の薬剤。[Scope of Claims] (11. Hair permanent finishing agent, A) (1)
) cationically activated cellulose and/or polytrimethylammonium methyl methacrylate, or (1
) 0.1 to 1.5% by weight of polyacrylic acid, polymethacrylic acid, carboxymethyl cellulose and hydrogen/or alginic acid; 0.1 to 3.0% by weight of ethanolamide and/or isozolopanolamide of saturated fatty acids; C) an amphoteric surfactant prepared by general formula (1) or (11); 0.05 to 0.8% by weight of the above, and L
)) An agent for reduction or oxidation processes, characterized in that it contains a combination of 0.05 to 1.5% by weight of fatty acid dimethylammonium betaine in which the number of carbon atoms in the fatty acid residue is 12 to 18. . 2 [Here, R3 is CH2-CH2-OH or CH2-
CI-(2-COOA(A-HlNa), R2 is CH2
-C00A, CH2-CH2-C00A, CH
2-CH2-0-CH2-COOA or CH2CH
2OCH2CH2C00A (A-H, Na), further R3 is a straight chain hydrocarbon residue having 7 to 18 carbon atoms,
Preferably C, R05, C9H, 9, C, f-1□3
Or hail C1□H35. (2) The drug according to claim 1, which contains a cationic cellulose ether represented by the following general formula as cationically activated cellulose. [Here, Rcell is an anhydroglucose unit, Y is an integer of 50 to 20,000, and R is an individual group represented by the following general formula. -(C2H40)m-(CH2CHO)n-(C2H4
0), -HOH3 (where m is an integer from 0 to 10, n is an integer from ○ to 3, and p is an integer from O to 1o.)] (3) The amphoteric surfactant has the following general formula: 3. The drug according to claim 1 or 2, which is a compound that causes hailstones. OCR'2COOA Coconut-〇-NH-CH,,-CH2-N-CH2-
CH2-OHCH2C00A (A=H, Na) (4) Any one of claims 1 to 3, characterized in that it has a viscosity of approximately 5 roomPa,s (millipascal seconds). Drugs listed in.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE19823207738 DE3207738A1 (en) | 1982-03-04 | 1982-03-04 | AGENT FOR PERMANENT DEFORMING OF HAIR |
DE3207738.6 | 1982-03-04 |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS58162513A true JPS58162513A (en) | 1983-09-27 |
JPH022854B2 JPH022854B2 (en) | 1990-01-19 |
Family
ID=6157269
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP58008612A Granted JPS58162513A (en) | 1982-03-04 | 1983-01-20 | Hair permanent treating agent |
Country Status (4)
Country | Link |
---|---|
JP (1) | JPS58162513A (en) |
DE (1) | DE3207738A1 (en) |
GB (1) | GB2116218B (en) |
IT (1) | IT1164628B (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS61286312A (en) * | 1985-06-14 | 1986-12-16 | Daicel Chem Ind Ltd | Waving lotion composition |
JPS6317817A (en) * | 1986-07-10 | 1988-01-25 | Sanyo Chem Ind Ltd | Shampoo composition |
JPH11130637A (en) * | 1997-10-30 | 1999-05-18 | Hoyu Co Ltd | Agent composition for permanent wave |
Families Citing this family (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CA1266829A (en) * | 1985-02-07 | 1990-03-20 | Du Yung Hsiung | Permanent wave neutralizer composition and method |
NL8601762A (en) * | 1986-07-07 | 1988-02-01 | Bouke Jan Lange | METHOD FOR CLEANING AND CONDITIONING AND ANY MEDICINAL TREATMENT OF HAIR AND SCALP, A TWO-PHASE SHAMPOO USABLE FOR THIS PURPOSE AND PACKAGING FOR IT. |
DE3820029A1 (en) * | 1988-06-13 | 1989-12-14 | Goldschmidt Ag Th | DERIVATIVES OF CARBOXYMETHYLCELLULOSE CONTAINING BETAINE GROUPS, THEIR PRODUCTION AND THEIR USE IN COSMETIC PREPARATIONS |
DE69118323T3 (en) * | 1990-11-22 | 2003-04-17 | Yanagita Co | Perm wave lotions and methods of using them |
DE4131992A1 (en) * | 1991-09-26 | 1993-04-01 | Wella Ag | FIXING AGENT AND METHOD FOR PERMANENT HAIR DEFORMING |
DE4406922C2 (en) * | 1994-02-28 | 2002-11-21 | Gabriele Wyeth Ohg Kosmetik Be | Hair treatment process |
DE19622999C1 (en) * | 1996-06-08 | 1997-12-11 | Wella Ag | Process and agent for permanent hair shaping |
FR2773072B1 (en) * | 1997-12-30 | 2001-03-23 | Oreal | MULTI-COMPONENT OXIDIZING AGENT AND PROCESS FOR THE PERMANENT DEFORMATION OF HAIR USING THE SAME |
-
1982
- 1982-03-04 DE DE19823207738 patent/DE3207738A1/en active Granted
-
1983
- 1983-01-20 JP JP58008612A patent/JPS58162513A/en active Granted
- 1983-02-07 GB GB08303271A patent/GB2116218B/en not_active Expired
- 1983-02-24 IT IT8347783A patent/IT1164628B/en active
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS61286312A (en) * | 1985-06-14 | 1986-12-16 | Daicel Chem Ind Ltd | Waving lotion composition |
JPH0380125B2 (en) * | 1985-06-14 | 1991-12-24 | Daicel Chem | |
JPS6317817A (en) * | 1986-07-10 | 1988-01-25 | Sanyo Chem Ind Ltd | Shampoo composition |
JPH0575722B2 (en) * | 1986-07-10 | 1993-10-21 | Sanyo Chemical Ind Ltd | |
JPH11130637A (en) * | 1997-10-30 | 1999-05-18 | Hoyu Co Ltd | Agent composition for permanent wave |
Also Published As
Publication number | Publication date |
---|---|
GB2116218A (en) | 1983-09-21 |
IT1164628B (en) | 1987-04-15 |
JPH022854B2 (en) | 1990-01-19 |
DE3207738A1 (en) | 1983-09-08 |
DE3207738C2 (en) | 1987-08-13 |
GB8303271D0 (en) | 1983-03-09 |
IT8347783A0 (en) | 1983-02-24 |
GB2116218B (en) | 1985-11-06 |
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