CN116139041A - Cationic color-protecting composition and color-protecting hair conditioner containing same - Google Patents

Cationic color-protecting composition and color-protecting hair conditioner containing same Download PDF

Info

Publication number
CN116139041A
CN116139041A CN202310016001.4A CN202310016001A CN116139041A CN 116139041 A CN116139041 A CN 116139041A CN 202310016001 A CN202310016001 A CN 202310016001A CN 116139041 A CN116139041 A CN 116139041A
Authority
CN
China
Prior art keywords
parts
color
psoralen
polyquaternium
protecting
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.)
Pending
Application number
CN202310016001.4A
Other languages
Chinese (zh)
Inventor
邓声量
黄家强
梁柳清
邓声敬
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Guangdong Zhilian Technology Development Co ltd
Original Assignee
Guangdong Zhilian Technology Development Co ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Guangdong Zhilian Technology Development Co ltd filed Critical Guangdong Zhilian Technology Development Co ltd
Priority to CN202310016001.4A priority Critical patent/CN116139041A/en
Publication of CN116139041A publication Critical patent/CN116139041A/en
Pending legal-status Critical Current

Links

Images

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/72Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/81Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
    • A61K8/817Compositions 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 a single or double bond to nitrogen or by a heterocyclic ring containing nitrogen; Compositions or derivatives of such polymers, e.g. vinylimidazol, vinylcaprolactame, allylamines (Polyquaternium 6)
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/46Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing sulfur
    • A61K8/463Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing sulfur containing sulfuric acid derivatives, e.g. sodium lauryl sulfate
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/92Oils, fats or waxes; Derivatives thereof, e.g. hydrogenation products thereof
    • A61K8/922Oils, fats or waxes; Derivatives thereof, e.g. hydrogenation products thereof of vegetable origin
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q5/00Preparations for care of the hair
    • A61Q5/004Preparations used to protect coloured hair
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q5/00Preparations for care of the hair
    • A61Q5/12Preparations containing hair conditioners
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K2800/00Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
    • A61K2800/40Chemical, physico-chemical or functional or structural properties of particular ingredients
    • A61K2800/54Polymers characterized by specific structures/properties
    • A61K2800/542Polymers characterized by specific structures/properties characterized by the charge
    • A61K2800/5424Polymers characterized by specific structures/properties characterized by the charge anionic
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K2800/00Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
    • A61K2800/40Chemical, physico-chemical or functional or structural properties of particular ingredients
    • A61K2800/59Mixtures
    • A61K2800/592Mixtures of compounds complementing their respective functions
    • A61K2800/5922At least two compounds being classified in the same subclass of A61K8/18
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02ATECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
    • Y02A50/00TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
    • Y02A50/30Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change

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)
  • Birds (AREA)
  • Epidemiology (AREA)
  • Chemical & Material Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Dermatology (AREA)
  • Cosmetics (AREA)

Abstract

The invention relates to the field of hair conditioners, in particular to a cationic color protecting composition and a color protecting hair conditioner containing the composition. The cationic color-protecting composition comprises the following components in parts by weight: 0.05-3 parts of polyquaternium-55, 0.05-4 parts of psoralen polyquaternium, 0.05-5 parts of sunflower seed oil amidopropyl dimethylamine lactate, 0.05-5 parts of PEG-2-dicamba seed oil amidoethyl methyl ammonium methyl sulfate and 0.05-6 parts of C18-C30 isoalkanamidopropyl ethyl dimethyl ammonium ethyl sulfate. The cation color-protecting composition-containing color-protecting hair conditioner is optimized and improved in conditioning performance and repairing performance of hair care, a new breakthrough is made in color-protecting efficacy, and the adopted cation color-protecting composition has the effects of protecting color and slowing down fading of dyed hair, and simultaneously has the effects of conditioning hair, repairing hair scales and moistening hair, so that the effect of the product is improved.

Description

Cationic color-protecting composition and color-protecting hair conditioner containing same
Technical Field
The invention relates to the field of hair conditioners, in particular to a cationic color protecting composition and a color protecting hair conditioner containing the composition.
Background
The simple and easy cosmetic means brings colorful life to us and brings some trouble to us at the same time of dyeing hair: why does freshly dyed hair "dulled out" for a long time? This has become a frequent complaint of consumers. How to keep the color after dyeing longer, which hair products have color protection function and how to verify the color protection claim of the products are popular research directions.
The permanent hair dyeing process can be briefly summarized as: the alkaline component in the hair dye opens the hair scale of the hair, the dye small molecular precursor, the dye coupling agent and the oxidant penetrate into the cortex layer of the hair together, oxidation condensation reaction occurs there, the dye small molecular precursor is oxidized and condensed into macromolecules with the dye coupling agent, and the macromolecules stay in the epidermis and the cortex layer of the hair fiber to display target color. Consumers who use permanent hair dyes generally want the hair to be permanently dyed or they want the bright color after dyeing to be maintained for a longer period of time to reduce the frequency of dyeing. In fact, however, neither hair dye permanently retains the color. The unavoidable factors such as hair washing, hair waving, sunlight irradiation and the like can cause the color of the dyed hair to drop and the luster to be reduced, wherein the hair washing and hair care is the first big 'basic murder' for causing the color drop after dyeing. In the hair washing and caring process, the short carbon chain surfactant in the common shampoo and the hair conditioner not only can increase the solubility of the dye in water, so that the dye is gradually transferred into the water from the surface of the hair, but also can open the hair scales, so that a large amount of dye in the hair conditioner is lost. In addition, damage to the hair surface and the resultant porous structure of the hair scale surface also accelerates dye loss. At this time, the decolorization effect of the shampoo and the conditioner is particularly remarkable. Some have been subjected to even two shampooing processes, the color of which has been far from the original post-dyeing color. Sunlight is also one of the causes of hair discoloration after dyeing. Ultraviolet rays in sunlight can damage hair fibers and hair scales, so that the hair scales are tilted, and the pores on the surfaces of the fibers are increased, thereby accelerating the falling of dyes in hair.
Currently, commercially available color-protecting alleged conditioners are less on the market, and most products are imported products, and have differences in applicability to asian hair quality. In addition, the existing commercial color-protecting hair conditioner still has certain defects in the formula structure, the formula cationic emulsifier is similar to the conventional hair conditioner in selection, and the quaternary ammonium salt of C16 or C18 is used, so that the short carbon chain cationic surfactant has strong surface activity, and the solubility of dye molecules in water can be increased, so that the dye permeates into the water from the hair surface layer; meanwhile, the short carbon chain cationic quaternary ammonium salt has no obvious effect on hair restoration, and long-term use of the short carbon chain cationic quaternary ammonium salt can not only play a role in color protection, but also continuously destroy hair scales and deepen the hair frizziness. In addition, one method of preventing post-dye fading in existing commercial color protection conditioners is to slow down the fading by simply adding an ultraviolet absorber. By combining with analysis of dye fading influence factors, the addition of an ultraviolet absorber can only weaken the color drop caused by sunlight irradiation, and cannot effectively slow down the drop of the dyed color integral caused by other factors. According to a permanent dye paste durability test method, the delta E total color difference change is measured, the color protection rate is calculated, and the fact that the existing color protection hair conditioner has the color protection rate of only 10-15% in the color protection performance is found, so that the requirements of consumers can not be met.
Disclosure of Invention
Aiming at the problems in the prior art, the invention aims to provide a safe, efficient and high-color-protection cationic color-protection composition and a color-protection hair conditioner containing the composition.
The aim of the invention is realized by adopting the following technical scheme:
in a first aspect, the present invention provides a cationic color care composition comprising, in parts by weight:
0.05-3 parts of polyquaternium-55, 0.05-4 parts of psoralen polyquaternium, 0.05-5 parts of sunflower seed oil amidopropyl dimethylamine lactate, 0.05-5 parts of PEG-2-dicamba seed oil amidoethyl methyl ammonium methyl sulfate and 0.05-6 parts of C18-C30 isoalkanamidopropyl ethyl dimethyl ammonium ethyl sulfate.
Preferably, the cationic color-protecting composition comprises the following components in parts by weight:
2 parts of polyquaternium-55, 2 parts of psoralen polyquaternium, 0.2 part of sunflower seed oil amidopropyl dimethylamine lactate, 0.6 part of PEG-2 di-white pond flower seed oil amidoethyl methyl ammonium methyl sulfate and 0.5 part of C18-C30 isoalkanamide propyl ethyl dimethyl ammonium ethyl sulfate.
Preferably, the cationic color-protecting composition comprises the following components in parts by weight:
2.5 parts of polyquaternium-55, 2.5 parts of psoralen polyquaternium, 0.6 part of sunflower seed oil amidopropyl dimethylamine lactate, 0.8 part of PEG-2 di-white pond flower seed oil amidoethyl methyl ammonium methyl sulfate and 0.8 part of C18-C30 isoalkanamide propyl ethyl dimethyl ammonium ethyl sulfate.
Preferably, the cationic color-protecting composition comprises the following components in parts by weight:
3 parts of polyquaternium-55, 3 parts of psoralen polyquaternium, 1 part of sunflower seed oil amidopropyl dimethylamine lactate, 1 part of PEG-2-di-white pond flower seed oil amidoethyl methyl ammonium methyl sulfate and 1 part of C18-C30 isoalkanamide propyl ethyl dimethyl ammonium ethyl sulfate.
Preferably, the cationic color-protecting composition comprises the following components in parts by weight:
4 parts of polyquaternium-55, 4 parts of psoralen polyquaternium, 1.2 parts of sunflower seed oil amidopropyl dimethylamine lactate, 1.5 parts of PEG-2 di-white pond flower seed oil amidoethyl methyl ammonium methyl sulfate and 1.5 parts of C18-C30 isoalkanamide propyl ethyl dimethyl ammonium ethyl sulfate.
In a second aspect, the present invention provides a color conditioner comprising a cationic color care composition, comprising, in parts by weight:
0.02-0.2 part of disodium ethylenediamine tetraacetate (EDTA disodium), 0.5-10 parts of glycerin, 0.1-3 parts of hydroxyethyl cellulose, 0.05-0.8 part of citric acid, 0.1-4 parts of behenyl trimethyl ammonium chloride, 0.1-4 parts of behenyl amidopropyl dimethylamine, 1-20 parts of polyquaternium-39, 1-25 parts of cationic color-protecting composition, 1-10 parts of cetostearyl alcohol, 0.1-5 parts of monoglyceride, 0.1-5 parts of coco dimethyl ammonium hydroxypropyl hydrolyzed wheat protein, 0.5-4 parts of aminoethyl aminopropyl polydimethylsiloxane, 0.5-4 parts of amino-terminal polydimethylsiloxane, 0.2-6 parts of polydimethylsiloxane, 0.1-5 parts of cyclopenta dimethicone, 0.1-5 parts of D-panthenol, 0.01-1.5 parts of PEG-14M, 0.2-0.8 parts of preservative, 0.2-1 and 50-100 parts of essence.
Preferably, the preparation method of the psoralen polyquaternium comprises the following steps:
s1, weighing 1, 3-dibromopropane, mixing in acetone, then adding sodium carbonate, and uniformly mixing to form a 1, 3-dibromopropane solution, wherein the mass ratio of the 1, 3-dibromopropane to the sodium carbonate to the acetone is 1:1:5-10; weighing 8-hydroxy psoralen, mixing in acetone to form 8-hydroxy psoralen solution, wherein the mass ratio of 8-hydroxy psoralen to acetone is 0.1-0.3:10;
s2, placing the 1, 3-dibromopropane solution into a water bath kettle at 45-50 ℃, dropwise adding the 8-hydroxy psoralen solution under the protection of inert gas, carrying out heat preservation reaction for 2-4 hours after the dropwise adding, and purifying and drying to obtain the bromopropyl psoralen; wherein the mass ratio of the 8-hydroxy psoralen solution to the 1, 3-dibromopropane solution is 1:2-3;
s3, mixing the bromopropyl psoralen and the ethyl 2- (diethylamino) acrylate into acetone, fully mixing, placing the mixture into a water bath kettle at 45-50 ℃, adding 2, 6-di-tert-butyl-p-cresol (polymerization inhibitor), reacting for 18-36 hours under heat preservation, filtering the product in ice water bath, and then drying in vacuum to obtain psoralen quaternary ammonium salt monomers; wherein the mass ratio of the bromopropyl psoralen to the 2- (diethylamino) ethyl acrylate to the acetone is 1.2-1.6:0.6-0.8:10-20; the mass ratio of the 2, 6-di-tert-butyl-p-cresol to the bromopropyl psoralen is 1.5-3:100;
s4, mixing psoralen quaternary ammonium salt monomers with ethanol, placing in a water bath kettle at 65-75 ℃, adding azodiisobutyronitrile under the protection of inert gas, then carrying out heat preservation reaction for 18-36h, filtering out precipitate obtained by the reaction, washing three times by using saturated sodium carbonate solution and ethanol in sequence, and carrying out vacuum drying to obtain psoralen polyquaternary ammonium salt; wherein the mass ratio of the psoralen quaternary ammonium salt monomer to the azodiisobutyronitrile to the ethanol is 2.4-2.8:0.06-0.1:20-30.
In a third aspect, the present invention provides a method for preparing a color conditioner comprising a cationic color composition, comprising the steps of:
step 1, weighing all the components according to the mass ratio of the components in the formula;
step 2, adding water into an emulsifying pot, adding the EDTA disodium, the citric acid, the glycerol and the hydroxyethyl cellulose weighed in the step 1 into the pot for dissolution and heating;
step 3, adding behentrimethyl ammonium chloride, behenamide propyl dimethylamine, C18-C30 isoalkanamide propyl ethyl dimethyl ammonium ethyl sulfate, cetostearyl alcohol and monoglyceride into an oil phase pot, and heating and melting;
step 4, heating the emulsifying pot to 75 ℃, pumping the oil in the oil phase pot into the emulsifying pot after all the oil phase pot substances are melted, homogenizing and emulsifying for 10 minutes, and keeping stirring;
step 5, adding polydimethylsiloxane, D-panthenol, coco dimethyl ammonium hydroxypropyl hydrolyzed wheat protein, aminoethyl aminopropyl polydimethylsiloxane, amino-terminal polydimethylsiloxane and cyclopenta-dimethicone into an emulsifying pot, homogenizing for 5 minutes, and keeping stirring;
step 6, adding polyquaternium-55 and psoralen polyquaternium, sunflower seed oil amide propyl dimethylamine lactate and PEG-2 di-white pond flower seed oil amide ethyl methyl ammonium methyl sulfate when the temperature is reduced to 60 ℃, and keeping stirring;
and 7, adding the quaternary ammonium salt-39, PEG-14M, preservative and essence when the temperature is reduced to 45 ℃, and stirring for 15-25 min to obtain the color-protecting hair conditioner containing the cationic color-protecting composition.
The beneficial effects of the invention are as follows:
1. the cation color-protecting composition-containing color-protecting hair conditioner is optimized and improved in conditioning performance and repairing performance of hair care, a new breakthrough is made in color-protecting efficacy, and the adopted cation color-protecting composition has the effects of protecting color and slowing down fading of dyed hair, and simultaneously has the effects of conditioning hair, repairing hair scales and moistening hair, so that the effect of the product is improved.
2. In the present invention, the cationic color care composition comprises polyquaternium-55, psoralen polyquaternium, sunflower seed oil amide propyl dimethylamine lactate, PEG-2 di-white pond flower seed oil amide ethyl methyl ammonium methyl sulfate and C18-C30 isoalkanamide propyl ethyl dimethyl ammonium ethyl sulfate. Wherein, psoralen polyquaternary ammonium salt belongs to a self-made polyquaternary ammonium salt, the substance adopts psoralen and 2- (diethylamino) ethyl acrylate to combine to form psoralen quaternary ammonium salt monomer, and then the product is obtained through free radical polymerization. Psoralen, also called corylifolia lactone, is an active ingredient extracted from fructus Psoraleae of Leguminosae, and has effect in increasing melanin. The invention grafts the psoralen polymer quaternary ammonium salt as a unique group on the quaternary ammonium salt, then participates in the polymerization of the quaternary ammonium salt, and the obtained psoralen polymer quaternary ammonium salt combines the advantages of the psoralen and the quaternary ammonium salt, and the subsequent detection shows that the psoralen polymer quaternary ammonium salt has very good promotion performance on the protection of the color and the reduction of the fading.
Drawings
The invention will be further described with reference to the accompanying drawings, in which embodiments do not constitute any limitation of the invention, and other drawings can be obtained by one of ordinary skill in the art without inventive effort from the following drawings.
FIG. 1 is a diagram showing the analysis of the hair salon half-head experiments of the color conditioner of examples 2-4 and comparative examples 1-2 of the present invention;
FIG. 2 is a graph showing the color difference of the cyclic care for permanent dyeing of the color-protecting conditioner of examples 1 to 4 and comparative examples 1 to 2 according to the present invention using an x-rite color difference meter;
FIG. 3 is a graph showing the color retention analysis of permanent dyeing of color hair conditioner of examples 1-4 and comparative examples 1-2 using an x-rite color difference meter;
fig. 4 is a comparative graph of the effect of the color conditioner and the commercial product provided by the present invention (the left side of the graph is a dyed picture, the middle is a picture treated in example 3 of the present invention, and the right side is a picture treated in commercial 2).
Detailed Description
The technical features, objects and advantages of the present invention will be more clearly understood from the following detailed description of the technical aspects of the present invention, but should not be construed as limiting the scope of the invention.
The starting materials, reagents or apparatus used in the following examples are all available from conventional commercial sources or may be obtained by methods known in the art unless otherwise specified.
The invention will be further described with reference to the following examples.
Example 1
A color conditioner comprising a cationic color care composition, comprising, in parts by weight:
0.02 part of disodium ethylenediamine tetraacetate (disodium EDTA), 3 parts of glycerol, 0.5 part of hydroxyethyl cellulose, 0.05 part of citric acid, 2 parts of behenyl trimethyl ammonium chloride, 1 part of behenyl amidopropyl dimethylamine, 1 part of polyquaternium-39, 2 parts of polyquaternium-55, 2 parts of psoralen polyquaternium, 0.2 part of sunflower seed oil amidopropyl dimethylamine lactate, 0.6 part of PEG-2-dicamba seed oil amidoethylmethyl ammonium methyl sulfate, 0.5 part of C18-C30 isoamyl amidopropyl ethyl dimethyl ammonium ethyl sulfate, 4 parts of cetostearyl alcohol, 0.2 part of monoglyceride, 0.2 part of coco dimethyl ammonium hydroxypropyl hydrolyzed wheat protein, 0.5 part of aminoethyl aminopropyl polydimethylsiloxane, 0.8 part of amino terminal polydimethylsiloxane, 1 part of polydimethylsiloxane, 2 parts of cyclopenta dimethicone, 0.2 parts of D-panthenol, 0.05 part of PEG-14M, 0.2 parts of preservative, 0.3 parts of deionized water and 38 parts of deionized water.
The preparation method of the psoralen polyquaternary ammonium salt comprises the following steps:
s1, weighing 1, 3-dibromopropane, mixing in acetone, then adding sodium carbonate, and uniformly mixing to form a 1, 3-dibromopropane solution, wherein the mass ratio of the 1, 3-dibromopropane to the sodium carbonate to the acetone is 1:1:8; weighing 8-hydroxy psoralen, mixing in acetone to form 8-hydroxy psoralen solution, wherein the mass ratio of 8-hydroxy psoralen to acetone is 0.2:10;
s2, placing the 1, 3-dibromopropane solution in a water bath kettle at 50 ℃, dropwise adding the 8-hydroxy psoralen solution under the protection of inert gas, carrying out heat preservation reaction for 3 hours after the dropwise adding, and purifying and drying to obtain the bromopropyl psoralen; wherein the mass ratio of the 8-hydroxy psoralen solution to the 1, 3-dibromopropane solution is 1:2.5;
s3, mixing the bromopropyl psoralen and the ethyl 2- (diethylamino) acrylate into acetone, fully mixing, placing the mixture into a water bath at 45 ℃, adding 2, 6-di-tert-butyl-p-cresol (polymerization inhibitor), reacting for 24 hours in a heat-preserving manner, filtering the product in an ice water bath, and then drying in vacuum to obtain a psoralen quaternary ammonium salt monomer; wherein the mass ratio of the bromopropyl psoralen to the 2- (diethylamino) ethyl acrylate to the acetone is 1.4:0.7:15; the mass ratio of the 2, 6-di-tert-butyl-p-cresol to the bromopropyl psoralen is 2.5:100;
s4, mixing psoralen quaternary ammonium salt monomers with ethanol, placing the mixture in a water bath kettle at 70 ℃, adding azodiisobutyronitrile under the protection of inert gas, then carrying out heat preservation reaction for 24 hours, filtering out precipitate obtained by the reaction, washing the precipitate with saturated sodium carbonate solution and ethanol for three times in sequence, and carrying out vacuum drying to obtain psoralen polyquaternary ammonium salt; wherein the mass ratio of the psoralen quaternary ammonium salt monomer to the azodiisobutyronitrile to the ethanol is 2.6:0.08:25.
The preparation method of the color protecting hair conditioner containing the cationic color protecting composition comprises the following steps:
step 1, weighing all the components according to the mass ratio of the components in the formula;
step 2, adding water into an emulsifying pot, adding the EDTA disodium, the citric acid, the glycerol and the hydroxyethyl cellulose weighed in the step 1 into the pot for dissolution and heating;
step 3, adding behentrimethyl ammonium chloride, behenamide propyl dimethylamine, C18-C30 isoalkanamide propyl ethyl dimethyl ammonium ethyl sulfate, cetostearyl alcohol and monoglyceride into an oil phase pot, and heating and melting;
step 4, heating the emulsifying pot to 75 ℃, pumping the oil in the oil phase pot into the emulsifying pot after all the oil phase pot substances are melted, homogenizing and emulsifying for 10 minutes, and keeping stirring;
step 5, adding polydimethylsiloxane, D-panthenol, coco dimethyl ammonium hydroxypropyl hydrolyzed wheat protein, aminoethyl aminopropyl polydimethylsiloxane, amino-terminal polydimethylsiloxane and cyclopenta-dimethicone into an emulsifying pot, homogenizing for 5 minutes, and keeping stirring;
step 6, adding polyquaternium-55 and psoralen polyquaternium, sunflower seed oil amide propyl dimethylamine lactate and PEG-2 di-white pond flower seed oil amide ethyl methyl ammonium methyl sulfate when the temperature is reduced to 60 ℃, and keeping stirring;
and 7, adding the quaternary ammonium salt-39, PEG-14M, preservative and essence when the temperature is reduced to 45 ℃, and stirring for 15-25 min to obtain the color-protecting hair conditioner containing the cationic color-protecting composition.
Example 2
The difference from example 1 is that the content of the ingredients of the color conditioner containing the cationic color composition is different, and the rest is the same as example 1 except that:
a color conditioner comprising a cationic color care composition, comprising, in parts by weight:
0.02 part of disodium ethylenediamine tetraacetate (disodium EDTA), 3 parts of glycerol, 0.5 part of hydroxyethyl cellulose, 0.05 part of citric acid, 2.5 parts of behenyl trimethyl ammonium chloride, 1.5 parts of behenyl amidopropyl dimethylamine, 2 parts of polyquaternium-39, 2.5 parts of polyquaternium-55, 2.5 parts of psoralen polyquaternium, 0.6 part of sunflower seed oil amidopropyl dimethylamine lactate, 0.8 part of PEG-2-bis-white pond flower seed oil amidoethyl methyl ammonium methyl sulfate, 0.8 part of C18-C30 isoamyl amidopropyl ethyl dimethyl ammonium ethyl sulfate, 5 parts of cetostearyl alcohol, 0.5 part of monoglyceride, 0.5 part of coco dimethyl ammonium hydroxypropyl hydrolyzed wheat protein, 0.8 part of aminoethyl aminopropyl polydimethylsiloxane, 1 part of amino end polydimethylsiloxane, 1 part of polydimethylsiloxane, 2 parts of cyclopentanol, 0.3 parts of D-panthenol, 0.06 part of PEG-14, 2.07 parts of a preservative, 0.3 parts of deionized water and 76 parts of deionized water.
Example 3
The difference from example 1 is that the content of the ingredients of the color conditioner containing the cationic color composition is different, and the rest is the same as example 1 except that:
a color conditioner comprising a cationic color care composition, comprising, in parts by weight:
0.02 part of disodium ethylenediamine tetraacetate (disodium EDTA), 3 parts of glycerol, 0.5 part of hydroxyethyl cellulose, 0.05 part of citric acid, 2.5 parts of behenyl trimethyl ammonium chloride, 2.5 parts of behenyl amidopropyl dimethylamine, 3 parts of polyquaternium-39, 3 parts of polyquaternium-55, 3 parts of psoralen polyquaternium, 1 part of sunflower seed oil amidopropyl dimethylamine lactate, 1 part of PEG-2-bis-platinum seed oil amidoethylmethyl ammonium methyl sulfate, 1 part of C18-C30 isoamyl amidopropyl ethyl dimethyl ammonium ethyl sulfate, 5 parts of cetostearyl alcohol, 0.5 part of monoglyceride, 0.5 part of cocodimethicone hydroxypropyl hydrolyzed wheat protein, 0.8 part of aminoethylaminopropyl polydimethylsiloxane, 1 part of amodimethicone, 1 part of dimethicone, 2 parts of cyclopentamethyl silicone, 0.3 part of D-alcohol, 0.06 part of PEG-14M, 0.2 part of preservative, 0.3 part of essence and 383 parts of deionized water.
Example 4
The difference from example 1 is that the content of the ingredients of the color conditioner containing the cationic color composition is different, and the rest is the same as example 1 except that:
0.02 part of disodium ethylenediamine tetraacetate (disodium EDTA), 3 parts of glycerol, 0.5 part of hydroxyethyl cellulose, 0.05 part of citric acid, 2.8 parts of behenyl trimethyl ammonium chloride, 2.5 parts of behenyl amidopropyl dimethylamine, 3 parts of polyquaternium-39, 4 parts of polyquaternium-55, 4 parts of psoralen polyquaternium, 1.2 parts of sunflower seed oil amidopropyl dimethylamine lactate, 1.5 parts of PEG-2-bis-white pond flower seed oil amidoethyl methyl ammonium methyl sulfate, 1.5 parts of C18-C30 isoamyl amidopropyl ethyl dimethyl ammonium ethyl sulfate, 5 parts of cetostearyl alcohol, 0.5 part of monoglyceride, 0.5 part of coco dimethyl ammonium hydroxypropyl hydrolyzed wheat protein, 0.8 part of aminoethyl aminopropyl polydimethylsiloxane, 1 part of amino end polydimethylsiloxane, 1 part of polydimethylsiloxane, 2 parts of cyclopenta-dimethicone, 0.3 parts of D-alcohol, 0.06 parts of PEG-14M, 0.2 parts of preservative, 70.27 parts of panthenol and deionized water.
Example 5
A color conditioner comprising a cationic color care composition, comprising, in parts by weight:
0.02 part of disodium ethylenediamine tetraacetate (disodium EDTA), 0.5 part of glycerin, 0.1 part of hydroxyethyl cellulose, 0.05 part of citric acid, 0.1 part of behenyl trimethyl ammonium chloride, 0.1 part of behenyl amidopropyl dimethylamine, 1 part of polyquaternium-39, 0.05 part of polyquaternium-55, 0.05 part of psoralen polyquaternium, 0.05 part of sunflower seed oil amidopropyl dimethylamine lactate, 0.05 part of PEG-2-bis-white pond flower seed oil amidoethyl methyl ammonium methyl sulfate, 0.05 part of C18-C30 isoamyl amidopropyl ethyl dimethyl ammonium ethyl sulfate, 1 part of cetostearyl alcohol, 0.1 part of monoglyceride, 0.1 part of coco dimethyl ammonium hydroxypropyl hydrolyzed wheat protein, 0.5 part of aminoethyl aminopropyl polydimethylsiloxane, 0.5 part of amino end polydimethylsiloxane, 0.2 part of polydimethylsiloxane, 0.1 part of cyclopentanol, 0.1 part of D-panthenol, 0.01-14, 0.2 part of PEG and 50 parts of a preservative.
Example 6
A color conditioner comprising a cationic color care composition, comprising, in parts by weight:
0.2 part of disodium ethylenediamine tetraacetate (disodium EDTA), 10 parts of glycerol, 3 parts of hydroxyethyl cellulose, 0.8 part of citric acid, 4 parts of behenyl trimethyl ammonium chloride, 4 parts of behenyl amidopropyl dimethylamine, 20 parts of polyquaternium-39, 3 parts of polyquaternium-55, 4 parts of psoralen polyquaternium, 5 parts of sunflower seed oil amidopropyl dimethylamine lactate, 5 parts of PEG-2-bis-white flower seed oil amidoethylmethyl ammonium methyl sulfate, 6 parts of C18-C30 isoamyl amidopropyl ethyl dimethyl ammonium ethyl sulfate, 10 parts of cetostearyl alcohol, 5 parts of monoglyceride, 5 parts of cocodimethyl ammonium hydroxypropyl hydrolyzed wheat protein, 4 parts of aminoethyl aminopropyl polydimethylsiloxane, 4 parts of amino end polydimethylsiloxane, 6 parts of polydimethylsiloxane, 5 parts of cyclopentanol, 5 parts of D-panthenol, 1.5 parts of PEG-14M, 0.8 part of preservative, 1 part of essence and 100 parts of deionized water.
Example 7
The difference from example 1 is that the preparation method of psoralen polyquaternium is different, and the rest is the same as example 1, except that:
the preparation method of the psoralen polyquaternary ammonium salt comprises the following steps:
s1, weighing 1, 3-dibromopropane, mixing in acetone, then adding sodium carbonate, and uniformly mixing to form a 1, 3-dibromopropane solution, wherein the mass ratio of the 1, 3-dibromopropane to the sodium carbonate to the acetone is 1:1:5; weighing 8-hydroxy psoralen, mixing in acetone to form 8-hydroxy psoralen solution, wherein the mass ratio of 8-hydroxy psoralen to acetone is 0.1:10;
s2, placing the 1, 3-dibromopropane solution in a water bath kettle at 45 ℃, dropwise adding the 8-hydroxy psoralen solution under the protection of inert gas, carrying out heat preservation reaction for 2 hours after the dropwise adding, and purifying and drying to obtain the bromopropyl psoralen; wherein the mass ratio of the 8-hydroxy psoralen solution to the 1, 3-dibromopropane solution is 1:2;
s3, mixing the bromopropyl psoralen and the ethyl 2- (diethylamino) acrylate into acetone, fully mixing, placing the mixture into a water bath at 45 ℃, adding 2, 6-di-tert-butyl-p-cresol (polymerization inhibitor), reacting for 18 hours in a heat-preserving manner, filtering the product in an ice water bath, and then drying in vacuum to obtain a psoralen quaternary ammonium salt monomer; wherein the mass ratio of the bromopropyl psoralen to the 2- (diethylamino) ethyl acrylate to the acetone is 1.2:0.6:10; the mass ratio of the 2, 6-di-tert-butyl-p-cresol to the bromopropyl psoralen is 1.5:100;
s4, mixing psoralen quaternary ammonium salt monomers with ethanol, placing the mixture in a water bath kettle at 65 ℃, adding azodiisobutyronitrile under the protection of inert gas, then carrying out heat preservation reaction for 18 hours, filtering out precipitate obtained by the reaction, washing the precipitate with saturated sodium carbonate solution and ethanol for three times in sequence, and carrying out vacuum drying to obtain psoralen polyquaternary ammonium salt; wherein the mass ratio of the psoralen quaternary ammonium salt monomer to the azodiisobutyronitrile to the ethanol is 2.4:0.06:20.
Example 8
The difference from example 1 is that the preparation method of psoralen polyquaternium is different, and the rest is the same as example 1, except that:
the preparation method of the psoralen polyquaternary ammonium salt comprises the following steps:
s1, weighing 1, 3-dibromopropane, mixing in acetone, then adding sodium carbonate, and uniformly mixing to form a 1, 3-dibromopropane solution, wherein the mass ratio of the 1, 3-dibromopropane to the sodium carbonate to the acetone is 1:1:10; weighing 8-hydroxy psoralen, mixing in acetone to form 8-hydroxy psoralen solution, wherein the mass ratio of 8-hydroxy psoralen to acetone is 0.3:10;
s2, placing the 1, 3-dibromopropane solution in a water bath kettle at 50 ℃, dropwise adding the 8-hydroxy psoralen solution under the protection of inert gas, carrying out heat preservation reaction for 4 hours after the dropwise adding, and purifying and drying to obtain the bromopropyl psoralen; wherein the mass ratio of the 8-hydroxy psoralen solution to the 1, 3-dibromopropane solution is 1:3;
s3, mixing the bromopropyl psoralen and the ethyl 2- (diethylamino) acrylate into acetone, fully mixing, placing the mixture into a water bath kettle at 50 ℃, adding 2, 6-di-tert-butyl-p-cresol (polymerization inhibitor), reacting for 36h under heat preservation, filtering the product in an ice water bath, and then drying in vacuum to obtain psoralen quaternary ammonium salt monomers; wherein the mass ratio of the bromopropyl psoralen to the 2- (diethylamino) ethyl acrylate to the acetone is 1.6:0.8:20; the mass ratio of the 2, 6-di-tert-butyl-p-cresol to the bromopropyl psoralen is 3:100;
s4, mixing psoralen quaternary ammonium salt monomers with ethanol, placing the mixture in a water bath kettle at 75 ℃, adding azodiisobutyronitrile under the protection of inert gas, then carrying out heat preservation reaction for 36 hours, filtering out precipitate obtained by the reaction, washing the precipitate with saturated sodium carbonate solution and ethanol for three times in sequence, and carrying out vacuum drying to obtain psoralen polyquaternary ammonium salt; wherein the mass ratio of the psoralen quaternary ammonium salt monomer to the azodiisobutyronitrile to the ethanol is 2.8:0.1:30.
Comparative example 1
A color conditioner comprising a cationic color care composition differs from example 3 in that no psoralen polyquaternium is added and the remainder is the same as in example 3.
Comparative example 2
A color conditioner comprising a cationic color care composition differs from example 3 in that the psoralen polyquaternium is replaced by polyquaternium-55, and the remainder is the same as in example 3.
Experimental example
The color conditioner ingredients containing cationic color care compositions prepared in examples 1-4 are listed in table 1 below:
TABLE 1 composition of different color conditioner
Figure SMS_1
Figure SMS_2
In order to prove the beneficial effects of the cationic color-protecting composition-containing color-protecting hair conditioner, the following design experiment is carried out on the color-protecting hair conditioner and the commercially available similar color-protecting hair conditioner:
1. conditioning performance (comb, softness, moisturization, etc.) of hair conditioner was evaluated by hair salon half-head test (Halftest)
2. The contact angle (contact angle) of the hair conditioner on the dyed hair surface was measured, the contact angle reflects the hydrophobicity of the hair, which is a hair damage mark, and the corresponding result of the contact angle change is as follows:
+ contact angle = increased contact angle, reduced hydrophobicity, and hair restored
- Δcontact angle = reduced contact angle, enhanced hydrophobicity, damaged hair
3. The combing performance and the tensile strength of the color-protecting hair conditioner and the commercially available similar color-protecting hair conditioner are measured by a universal tester
4. The color difference of the dyed hair after care using the present invention was compared using an x-rite color difference meter for permanent dyeing (Color Fading Experiment of Permanent Hair Dye) test, characterized by the color difference symbol Δe, which is defined as the total color difference of the sample, the greater the Δe number, indicating a greater color difference and a lower degree of color protection. The corresponding results of the color difference calculation formula and the variation are as follows:
ΔE=[△L^2+△a^2+△b^2]^1/2
the larger ΔE, the greater the color difference, indicating a higher degree of hair color fade;
the smaller ΔE, the smaller the color difference, indicating a lower degree of hair color fade;
wherein L, a, b have the meanings: l represents color brightness, a represents color redness-greenness, and b represents color yellowness-blueness.
The color protection rate is calculated through the change of the total color difference delta E, and the calculation formula is as follows:
color retention% = [ (Δe control- Δe experiment)/Δe control ] x100%
The color conditioner and the commercial color conditioner provided in examples 1 to 4 of the present invention were used as comparative examples (comparative example 1 is commercial 1, comparative example 2 is commercial 2), and are specifically as follows:
test results:
1. hair salon half head experiment:
half head test vs. combination referring to fig. 1, from the combination in fig. 1, it can be derived: comparative examples 1 and 2 contained 3 sets of test data, example 2 (labeled 2 in fig. 1), example 3 (labeled 3 in fig. 1), example 4 (labeled 4 in fig. 1), and comparative example 1 (labeled S1 in fig. 1), and comparative example 2 ((labeled S2 in fig. 1), and the data sets were each plotted as average values based on the similarity of the evaluation data, and the results are shown in fig. 1 below.
As can be seen from the curves of the radar chart, the formula of the example of the invention is superior to the commercial products in most indexes, and has remarkable improvement on softness of wet hair, detangling of tips of dry hair, smoothness of dry hair and freshness of dry hair. The hair conditioner provided by the invention has obviously improved hair care effect; and is superior to the commercial hair conditioner of the same type.
2. Contact angle test:
the hair dye containing the red basic dye as the main component is used for dyeing natural black hair into reddish brown, and hair is continuously treated for 5 times by using the hair conditioner, so that the result shows that the contact angle of the hair using the hair conditioner is obviously increased, the hair scales on the surface layer of the hair are obviously repaired, and the hydrophobicity is enhanced; the hair contact angles of the hair conditioner of the comparative example 1 and the hair conditioner of the comparative example 2 are not obviously changed, which indicates that the hair is not repaired and the hydrophobicity is not obviously changed.
TABLE 2 contact angle measurements of different color conditioners
Figure SMS_3
3. Instrument testing
The physical and chemical indicators of example formulations 1, 2, 3, 4 and comparative examples 1, 2, were tested for combing properties, tensile strength (breaking force) using an instrument. The specific test results are shown in Table 3 below.
TABLE 3 Performance detection of different color conditioners
Figure SMS_4
4. Fading experiment
According to fig. 2 and 3, according to the fading experiment test of permanent dyeing, after the color protection hair conditioner similar to the commercial color protection hair conditioner in 4 examples is treated for 10 times of circulation, the color protection rate is improved by 25-50% compared with the control group (without color protection combined raw materials), namely the color protection hair conditioner has a certain effect of protecting the color and slowing down the color loss. From fig. 3, we can also see that after 10 cycles of treatment with the color conditioner containing the cationic color-protecting composition of the present invention, the color-protecting rate of the example formulation is significantly higher than that of the hair conditioner of comparative examples 1 and 2 by 20-25%, indicating that the color-protecting performance of the color conditioner of the present invention is significantly better than that of the commercial products.
Finally, it should be noted that the above embodiments are only for illustrating the technical solution of the present invention, and not for limiting the scope of the present invention, and although the present invention has been described in detail with reference to the preferred embodiments, it should be understood by those skilled in the art that modifications or equivalent substitutions can be made to the technical solution of the present invention without departing from the spirit and scope of the technical solution of the present invention.

Claims (8)

1. A cationic color-protecting composition, characterized by comprising, in parts by weight:
0.05-3 parts of polyquaternium-55, 0.05-4 parts of psoralen polyquaternium, 0.05-5 parts of sunflower seed oil amidopropyl dimethylamine lactate, 0.05-5 parts of PEG-2-dicamba seed oil amidoethyl methyl ammonium methyl sulfate and 0.05-6 parts of C18-C30 isoalkanamidopropyl ethyl dimethyl ammonium ethyl sulfate.
2. The cationic color-protecting composition according to claim 1, wherein the cationic color-protecting composition comprises, in parts by weight:
2 parts of polyquaternium-55, 2 parts of psoralen polyquaternium, 0.2 part of sunflower seed oil amidopropyl dimethylamine lactate, 0.6 part of PEG-2 di-white pond flower seed oil amidoethyl methyl ammonium methyl sulfate and 0.5 part of C18-C30 isoalkanamide propyl ethyl dimethyl ammonium ethyl sulfate.
3. The cationic color-protecting composition according to claim 1, wherein the cationic color-protecting composition comprises, in parts by weight:
2.5 parts of polyquaternium-55, 2.5 parts of psoralen polyquaternium, 0.6 part of sunflower seed oil amidopropyl dimethylamine lactate, 0.8 part of PEG-2 di-white pond flower seed oil amidoethyl methyl ammonium methyl sulfate and 0.8 part of C18-C30 isoalkanamide propyl ethyl dimethyl ammonium ethyl sulfate.
4. The cationic color-protecting composition according to claim 1, wherein the cationic color-protecting composition comprises, in parts by weight:
3 parts of polyquaternium-55, 3 parts of psoralen polyquaternium, 1 part of sunflower seed oil amidopropyl dimethylamine lactate, 1 part of PEG-2-di-white pond flower seed oil amidoethyl methyl ammonium methyl sulfate and 1 part of C18-C30 isoalkanamide propyl ethyl dimethyl ammonium ethyl sulfate.
5. The cationic color-protecting composition according to claim 1, wherein the cationic color-protecting composition comprises, in parts by weight:
4 parts of polyquaternium-55, 4 parts of psoralen polyquaternium, 1.2 parts of sunflower seed oil amidopropyl dimethylamine lactate, 1.5 parts of PEG-2 di-white pond flower seed oil amidoethyl methyl ammonium methyl sulfate and 1.5 parts of C18-C30 isoalkanamide propyl ethyl dimethyl ammonium ethyl sulfate.
6. A color conditioner comprising a cationic color care composition according to any one of claims 1 to 5, comprising, in parts by weight:
0.02-0.2 part of disodium ethylenediamine tetraacetate (EDTA disodium), 0.5-10 parts of glycerin, 0.1-3 parts of hydroxyethyl cellulose, 0.05-0.8 part of citric acid, 0.1-4 parts of behenyl trimethyl ammonium chloride, 0.1-4 parts of behenyl amidopropyl dimethylamine, 1-20 parts of polyquaternium-39, 1-25 parts of cationic color-protecting composition, 1-10 parts of cetostearyl alcohol, 0.1-5 parts of monoglyceride, 0.1-5 parts of coco dimethyl ammonium hydroxypropyl hydrolyzed wheat protein, 0.5-4 parts of aminoethyl aminopropyl polydimethylsiloxane, 0.5-4 parts of amino-terminal polydimethylsiloxane, 0.2-6 parts of polydimethylsiloxane, 0.1-5 parts of cyclopenta dimethicone, 0.1-5 parts of D-panthenol, 0.01-1.5 parts of PEG-14M, 0.2-0.8 parts of preservative, 0.2-1 and 50-100 parts of essence.
7. The color protecting conditioner of claim 6, wherein the method for preparing the psoralen polyquaternium comprises the following steps:
s1, weighing 1, 3-dibromopropane, mixing in acetone, then adding sodium carbonate, and uniformly mixing to form a 1, 3-dibromopropane solution, wherein the mass ratio of the 1, 3-dibromopropane to the sodium carbonate to the acetone is 1:1:5-10; weighing 8-hydroxy psoralen, mixing in acetone to form 8-hydroxy psoralen solution, wherein the mass ratio of 8-hydroxy psoralen to acetone is 0.1-0.3:10;
s2, placing the 1, 3-dibromopropane solution into a water bath kettle at 45-50 ℃, dropwise adding the 8-hydroxy psoralen solution under the protection of inert gas, carrying out heat preservation reaction for 2-4 hours after the dropwise adding, and purifying and drying to obtain the bromopropyl psoralen; wherein the mass ratio of the 8-hydroxy psoralen solution to the 1, 3-dibromopropane solution is 1:2-3;
s3, mixing the bromopropyl psoralen and the ethyl 2- (diethylamino) acrylate into acetone, fully mixing, placing the mixture into a water bath kettle at 45-50 ℃, adding 2, 6-di-tert-butyl-p-cresol (polymerization inhibitor), reacting for 18-36 hours under heat preservation, filtering the product in ice water bath, and then drying in vacuum to obtain psoralen quaternary ammonium salt monomers; wherein the mass ratio of the bromopropyl psoralen to the 2- (diethylamino) ethyl acrylate to the acetone is 1.2-1.6:0.6-0.8:10-20; the mass ratio of the 2, 6-di-tert-butyl-p-cresol to the bromopropyl psoralen is 1.5-3:100;
s4, mixing psoralen quaternary ammonium salt monomers with ethanol, placing in a water bath kettle at 65-75 ℃, adding azodiisobutyronitrile under the protection of inert gas, then carrying out heat preservation reaction for 18-36h, filtering out precipitate obtained by the reaction, washing three times by using saturated sodium carbonate solution and ethanol in sequence, and carrying out vacuum drying to obtain psoralen polyquaternary ammonium salt; wherein the mass ratio of the psoralen quaternary ammonium salt monomer to the azodiisobutyronitrile to the ethanol is 2.4-2.8:0.06-0.1:20-30.
8. A method of preparing a color conditioner comprising a cationic color care composition according to claim 6, comprising the steps of:
step 1, weighing all the components according to the mass ratio of the components in the formula;
step 2, adding water into an emulsifying pot, adding the EDTA disodium, the citric acid, the glycerol and the hydroxyethyl cellulose weighed in the step 1 into the pot for dissolution and heating;
step 3, adding behentrimethyl ammonium chloride, behenamide propyl dimethylamine, C18-C30 isoalkanamide propyl ethyl dimethyl ammonium ethyl sulfate, cetostearyl alcohol and monoglyceride into an oil phase pot, and heating and melting;
step 4, heating the emulsifying pot to 75 ℃, pumping the oil in the oil phase pot into the emulsifying pot after all the oil phase pot substances are melted, homogenizing and emulsifying for 10 minutes, and keeping stirring;
step 5, adding polydimethylsiloxane, D-panthenol, coco dimethyl ammonium hydroxypropyl hydrolyzed wheat protein, aminoethyl aminopropyl polydimethylsiloxane, amino-terminal polydimethylsiloxane and cyclopenta-dimethicone into an emulsifying pot, homogenizing for 5 minutes, and keeping stirring;
step 6, adding polyquaternium-55 and psoralen polyquaternium, sunflower seed oil amide propyl dimethylamine lactate and PEG-2 di-white pond flower seed oil amide ethyl methyl ammonium methyl sulfate when the temperature is reduced to 60 ℃, and keeping stirring;
and 7, adding the quaternary ammonium salt-39, PEG-14M, preservative and essence when the temperature is reduced to 45 ℃, and stirring for 15-25 min to obtain the color-protecting hair conditioner containing the cationic color-protecting composition.
CN202310016001.4A 2023-01-05 2023-01-05 Cationic color-protecting composition and color-protecting hair conditioner containing same Pending CN116139041A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN202310016001.4A CN116139041A (en) 2023-01-05 2023-01-05 Cationic color-protecting composition and color-protecting hair conditioner containing same

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN202310016001.4A CN116139041A (en) 2023-01-05 2023-01-05 Cationic color-protecting composition and color-protecting hair conditioner containing same

Publications (1)

Publication Number Publication Date
CN116139041A true CN116139041A (en) 2023-05-23

Family

ID=86361269

Family Applications (1)

Application Number Title Priority Date Filing Date
CN202310016001.4A Pending CN116139041A (en) 2023-01-05 2023-01-05 Cationic color-protecting composition and color-protecting hair conditioner containing same

Country Status (1)

Country Link
CN (1) CN116139041A (en)

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0192211A (en) * 1987-10-03 1989-04-11 Goou Kagaku Kogyo Kk Cationic/ampholytic polymer having conditioning effect
US5427779A (en) * 1987-12-07 1995-06-27 Nunc A/S Modification of polymer surfaces and molecular immobilization by photoreaction
CN101780019A (en) * 2010-02-09 2010-07-21 广东名臣有限公司 Conditioning shampoo composition with hair brightening effect
CN104188833A (en) * 2009-02-05 2014-12-10 罗地亚管理公司 Aqueous composition suitable as shampoo
CN109745254A (en) * 2017-11-05 2019-05-14 达威控股有限公司 It is a kind of have effects that scalp care without silicone oil shampoo and preparation method thereof

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0192211A (en) * 1987-10-03 1989-04-11 Goou Kagaku Kogyo Kk Cationic/ampholytic polymer having conditioning effect
US5427779A (en) * 1987-12-07 1995-06-27 Nunc A/S Modification of polymer surfaces and molecular immobilization by photoreaction
CN104188833A (en) * 2009-02-05 2014-12-10 罗地亚管理公司 Aqueous composition suitable as shampoo
CN101780019A (en) * 2010-02-09 2010-07-21 广东名臣有限公司 Conditioning shampoo composition with hair brightening effect
CN109745254A (en) * 2017-11-05 2019-05-14 达威控股有限公司 It is a kind of have effects that scalp care without silicone oil shampoo and preparation method thereof

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
胡心宽: "《有机化学》", 中国医药科技出版社, pages: 200 *

Similar Documents

Publication Publication Date Title
TW201713308A (en) Method for processing hair and kit thereof
CN111297720B (en) Natural edible shampoo and preparation method thereof
US20100322888A1 (en) Emulsion Composition for Hair Treating Agents
CN112587424A (en) A hair composition with effects of protecting color and hair, and its preparation method
US4590249A (en) Cationic ampholytic tetrapolymers and cosmetic compositions containing them
CN106102701A (en) Oxide hair dye, the manufacture method of oxidation hair-dye intermixture and oxidation hair-dye method
CN102429835B (en) Keratin hairspray for hair and modeling products for hair
CN109528558B (en) Wet tissue feed liquid for hair with hair strengthening and toughening functions
CN116139041A (en) Cationic color-protecting composition and color-protecting hair conditioner containing same
CN106265347B (en) A kind of Haircare composition and its application based on marine bioactivity object
JP3606490B2 (en) Hairdressing resin composition
CN116135201A (en) Washing and caring product for improving hair drying speed and fluffiness after washing and preparation method thereof
CN109718167A (en) A kind of hand lotion and preparation method thereof with maintenance and moisture-keeping efficacy
JPH0553771B2 (en)
CN113730274A (en) Multifunctional fast black dyeing gel and preparation method thereof
AU2004206759A1 (en) Composition for permanent dyeing of keratinous fibers
CN113520947A (en) Color-fixing hair-care composition and preparation and application thereof
CN112402301A (en) Silicone-oil-free shampoo composition with softening and repairing effects and preparation method and application thereof
CN110025552B (en) Amino acid shampoo capable of increasing tensile strength and elongation of hair and preparation method thereof
CN116687770A (en) A hair care composition containing potassium iodide and its preparation method
CN116115514B (en) Hair-care plant protein composition and preparation method and application thereof
CN114983888B (en) Permanent gel hair dye and application method thereof
CN117481999A (en) Hair care composition for repairing damaged hair and preparation method thereof
CN117357439B (en) Washing and caring composition applied to fixation after dyeing and preparation method thereof
CN113143801B (en) Antioxidant scalp isolation muscle base solution and hair dye and preparation method thereof

Legal Events

Date Code Title Description
PB01 Publication
PB01 Publication
SE01 Entry into force of request for substantive examination
SE01 Entry into force of request for substantive examination