US2236970A - Remover for artificial colors from hair - Google Patents
Remover for artificial colors from hair Download PDFInfo
- Publication number
- US2236970A US2236970A US132295A US13229537A US2236970A US 2236970 A US2236970 A US 2236970A US 132295 A US132295 A US 132295A US 13229537 A US13229537 A US 13229537A US 2236970 A US2236970 A US 2236970A
- Authority
- US
- United States
- Prior art keywords
- hair
- sulphonated
- oil
- color
- artificial
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 239000003086 colorant Substances 0.000 title description 4
- 239000000463 material Substances 0.000 description 29
- 239000000975 dye Substances 0.000 description 19
- 239000000203 mixture Substances 0.000 description 16
- 150000007524 organic acids Chemical class 0.000 description 14
- BDHFUVZGWQCTTF-UHFFFAOYSA-N sulfonic acid Chemical group OS(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-N 0.000 description 12
- 230000037308 hair color Effects 0.000 description 11
- 239000003921 oil Substances 0.000 description 11
- 235000019198 oils Nutrition 0.000 description 11
- 239000002904 solvent Substances 0.000 description 10
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 9
- 239000000470 constituent Substances 0.000 description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
- 238000004043 dyeing Methods 0.000 description 7
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 5
- 239000002184 metal Substances 0.000 description 5
- 229910052751 metal Inorganic materials 0.000 description 5
- YGSDEFSMJLZEOE-UHFFFAOYSA-N salicylic acid Chemical compound OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 description 5
- 239000001117 sulphuric acid Substances 0.000 description 5
- 235000011149 sulphuric acid Nutrition 0.000 description 5
- DHMQDGOQFOQNFH-UHFFFAOYSA-N Glycine Chemical class NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 description 4
- 239000002253 acid Substances 0.000 description 4
- 150000007513 acids Chemical class 0.000 description 4
- 239000004359 castor oil Substances 0.000 description 4
- 235000019438 castor oil Nutrition 0.000 description 4
- 150000002191 fatty alcohols Chemical class 0.000 description 4
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 4
- -1 mono- Chemical class 0.000 description 4
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
- 238000001035 drying Methods 0.000 description 3
- 150000002739 metals Chemical class 0.000 description 3
- 230000035515 penetration Effects 0.000 description 3
- 235000013311 vegetables Nutrition 0.000 description 3
- WHBMMWSBFZVSSR-UHFFFAOYSA-N 3-hydroxybutyric acid Chemical compound CC(O)CC(O)=O WHBMMWSBFZVSSR-UHFFFAOYSA-N 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- 239000003513 alkali Substances 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 238000004040 coloring Methods 0.000 description 2
- 235000002864 food coloring agent Nutrition 0.000 description 2
- 235000013905 glycine and its sodium salt Nutrition 0.000 description 2
- 239000000118 hair dye Substances 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 229940097789 heavy mineral oil Drugs 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- 235000005985 organic acids Nutrition 0.000 description 2
- 150000007530 organic bases Chemical class 0.000 description 2
- FJKROLUGYXJWQN-UHFFFAOYSA-N papa-hydroxy-benzoic acid Natural products OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 2
- 229960004889 salicylic acid Drugs 0.000 description 2
- FSYKKLYZXJSNPZ-UHFFFAOYSA-N sarcosine Chemical compound C[NH2+]CC([O-])=O FSYKKLYZXJSNPZ-UHFFFAOYSA-N 0.000 description 2
- 210000004761 scalp Anatomy 0.000 description 2
- 150000005846 sugar alcohols Polymers 0.000 description 2
- 235000015112 vegetable and seed oil Nutrition 0.000 description 2
- 239000008158 vegetable oil Substances 0.000 description 2
- SBASXUCJHJRPEV-UHFFFAOYSA-N 2-(2-methoxyethoxy)ethanol Chemical compound COCCOCCO SBASXUCJHJRPEV-UHFFFAOYSA-N 0.000 description 1
- XNWFRZJHXBZDAG-UHFFFAOYSA-N 2-METHOXYETHANOL Chemical compound COCCO XNWFRZJHXBZDAG-UHFFFAOYSA-N 0.000 description 1
- POAOYUHQDCAZBD-UHFFFAOYSA-N 2-butoxyethanol Chemical compound CCCCOCCO POAOYUHQDCAZBD-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- IAJILQKETJEXLJ-UHFFFAOYSA-N Galacturonsaeure Natural products O=CC(O)C(O)C(O)C(O)C(O)=O IAJILQKETJEXLJ-UHFFFAOYSA-N 0.000 description 1
- 239000004471 Glycine Substances 0.000 description 1
- 235000004347 Perilla Nutrition 0.000 description 1
- 244000124853 Perilla frutescens Species 0.000 description 1
- 241000220324 Pyrus Species 0.000 description 1
- 108010077895 Sarcosine Proteins 0.000 description 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
- IAJILQKETJEXLJ-QTBDOELSSA-N aldehydo-D-glucuronic acid Chemical compound O=C[C@H](O)[C@@H](O)[C@H](O)[C@H](O)C(O)=O IAJILQKETJEXLJ-QTBDOELSSA-N 0.000 description 1
- 150000007933 aliphatic carboxylic acids Chemical class 0.000 description 1
- 239000010775 animal oil Substances 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 230000001680 brushing effect Effects 0.000 description 1
- 150000001720 carbohydrates Chemical class 0.000 description 1
- 235000014633 carbohydrates Nutrition 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 230000001143 conditioned effect Effects 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 235000005687 corn oil Nutrition 0.000 description 1
- 239000002285 corn oil Substances 0.000 description 1
- 235000012343 cottonseed oil Nutrition 0.000 description 1
- 239000002385 cottonseed oil Substances 0.000 description 1
- 230000002939 deleterious effect Effects 0.000 description 1
- 229940028356 diethylene glycol monobutyl ether Drugs 0.000 description 1
- XXJWXESWEXIICW-UHFFFAOYSA-N diethylene glycol monoethyl ether Chemical compound CCOCCOCCO XXJWXESWEXIICW-UHFFFAOYSA-N 0.000 description 1
- 229940075557 diethylene glycol monoethyl ether Drugs 0.000 description 1
- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 229940097043 glucuronic acid Drugs 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- 230000003806 hair structure Effects 0.000 description 1
- 230000000266 injurious effect Effects 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 230000007794 irritation Effects 0.000 description 1
- 239000010699 lard oil Substances 0.000 description 1
- 239000000944 linseed oil Substances 0.000 description 1
- 235000021388 linseed oil Nutrition 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- 125000001421 myristyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 235000019645 odor Nutrition 0.000 description 1
- 239000004006 olive oil Substances 0.000 description 1
- 235000008390 olive oil Nutrition 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- JCGNDDUYTRNOFT-UHFFFAOYSA-N oxolane-2,4-dione Chemical compound O=C1COC(=O)C1 JCGNDDUYTRNOFT-UHFFFAOYSA-N 0.000 description 1
- 125000000913 palmityl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 235000021017 pears Nutrition 0.000 description 1
- 230000000750 progressive effect Effects 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- 238000011268 retreatment Methods 0.000 description 1
- 239000012487 rinsing solution Substances 0.000 description 1
- FSYKKLYZXJSNPZ-UHFFFAOYSA-M sarcosinate Chemical compound CNCC([O-])=O FSYKKLYZXJSNPZ-UHFFFAOYSA-M 0.000 description 1
- 229940043230 sarcosine Drugs 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 229960004418 trolamine Drugs 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/92—Oils, fats or waxes; Derivatives thereof, e.g. hydrogenation products thereof
- A61K8/922—Oils, fats or waxes; Derivatives thereof, e.g. hydrogenation products thereof of vegetable origin
-
- 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
- A61K8/46—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing sulfur
- A61K8/466—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing sulfur containing sulfonic acid derivatives; Salts
-
- 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
- A61Q5/08—Preparations for bleaching the hair
-
- Y—GENERAL 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
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S424/00—Drug, bio-affecting and body treating compositions
- Y10S424/03—Hair bleach
-
- Y—GENERAL 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
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S424/00—Drug, bio-affecting and body treating compositions
- Y10S424/06—Chelate
Definitions
- This invention relates to color removers and more particularly to removers for the artificial colors of the metallic and vegetable dye type used in dyeing hair, and particularly living human hair.
- I may produce a hair dye or hair color remover which is especially suitable for the removal of metallic dyes, metallic hair color restorers and of many vegetable dyes and which is free from the objections inherent in the known artificial color removers for hair.
- the color remover embodying my invention comprises a sulphonated oleaginous material, such as a sulphonated 011 or oily material, containing free sulphonic acid groups, and may be used alone or in aqueous solution; preferably, however, I use it in combination with an organic acid or a solvent which exhibits mutualsolvent capacity for water, the sulphonated oleaginous material and the organic acid or with both.
- the solvent when used, appears to promote penetration and facilitate subsequent removal of the composition and dye; and the organic acid appears to improve penetration and promote the formation of a removable dye complex.
- This artificial color remover is particularly suitable for living human hair and is pears to properly condition the hair to render it immediately susceptible to recoloring or redyeing.
- the sulphonated oleaginous material employed in my novel composition may suitably be a sulphonated vegetable oil, 'anima1 oil, or heavy mineral oil, or a sulphonated higher fatty alcohol, to
- suflicient alkali such as sodium hydroxide or an organic base such as mono-, dior tri-ethanolamine has been added to neutralize substantially all of the free sulphuric acid.
- the amount of alkali which is added to the sulphonic acid derivative may be sufficient to neutralize not only all of the free sulphuric acid but some of the free sulphonic groups as well.
- it is essential that the sulphonated oleaginous material contain some free sulphonic acid groups and preferably all of them. Oleaginous material sulphonated to any desired extent may beused. I have found that oleaginous materials sulphonated to the extent of 6 to 15% to be highly eifective.
- the oleaginous material subjected to sulphonation for use may be of any suitable character; thus it maybe a vegetable oil, such as the nondrying oils, castor oil, olive oil, and the like; the semi-drying oils, cottonseed oil, corn oil and the like; or the drying oils, linseed oil, perilla oil and the like; an animal oil, such as lard oil or commercial hydrogenated oils; or a mineral oil, preferably a heavy mineral oil distillate; or. higher fatty alcohols, such as lauryl, cetyl, myristyl and like fatty alcohols having 6 to 8 or more and preferably 12 or more carbon atoms in the carbon chain.
- a vegetable oil such as the nondrying oils, castor oil, olive oil, and the like
- the semi-drying oils, cottonseed oil, corn oil and the like or the drying oils, linseed oil, perilla oil and the like
- an animal oil such as lard oil or commercial hydrogenated oils
- the organic acids employed in my novel composition are acids which are capable of forming Water solublecompounds or complexes with the highly effective in removing even the artificial variousmetals ordinarily used as mordants in dyeing hair, such as copper and iron.
- aromatic carboxylic acids such as salicyclic acid
- aliphatic carboxylic acids such as tartaric, lactic, citric, beta hydroxy butyric acid
- glycollic and malic monoand di-baslc acidsderived from carbohydrates such as gluconlc and saccharic acids; aldehyde-hydroxy-acids such as glucuronic acid; or amino acetic acids such as glycocoll (glycine) and methyl glycocoll (sarcosine) and like acids may be used.
- the common solvents employed in carrying out the invention are preferably organic solvents which are mutually soluble'in water and in the sulphonated oil or oily material and the organic acid embodied in my invention.
- Suitable solvents which may be used in carrying out the invention are glycerine, ethylene glycol and diethylene glycol; the alcohol ethers such as ethylene glycol mono-methyl ether. ethylene 81ycol mono-ethyl ether, ethylene glycol monobutyl ether, diethylene glycol mono-methyl ether, diethylene glycol mono-ethyl ether, diethylene glycol mono-butyl ether, and the like.
- compositions embodying my invention have been Under some conditions, as when the hair is dyed with a mixture of dyes of the metal and organic base types, the color or dye remover embodying my invention may remove substantially all of the metal dye but may not remove all of the organic dye and thus leave the hair with an undesirable shade. Even under these conditions the color remover leaves the hair in a condition for immediate retreatment with a dye for redyeing the hair to a desired shade or to modify the oil-shade. If desired, I may incorporate with my color remover a dye, suitably one of the wellknown progressive type and thus simultaneously redye the conditioned hair and thereby prevent the formation of ugly off-shades which may result from the removal of only part of a mixed dye.
- the treatment above described is preferably repeated until all of the dye has been removed. Usually only a singletreatment is necessary.
- a composition for removing artificial metallic hair coloring material from hair comprising a sulphonated oleaginous material containing free sulphonic acid groups as the active hair colorremoving constituent and containing no free sulphuric acid.
- a composition for removing artificial metallic hair coloring material from hair comprising sulphonated castor oil containing free sulphonic acid groups as the active hair color-removing constituent.
- the compostion is heated moderately, say to 100 F. to 125 F. or slightly higher, and is applied .in the heated state to the hair containing the artificial color either by the fingers or by brushing until the hair is thoroughly wetted.
- the air saturated with this composition is then warmed or heatedto a tolerable, high temperature in any suitable manner as by a heat lamp, hot towels, steamer or the like. This heating is continued for a suitable period, usually in the order of thirty to sixty minutes depending on the type of coloring material to be removed from the hair, the type and coarseness of the hair and other contributing factors.
- a composition for removing artificial metallic hair coloring material from hair comprising a sulphonated oleaginous material containing free sulphonic acid groups asthe active hair colorremoving constituent and an organic acid capable of forming soluble complexes or compounds with the various metals used in the dyeing art.
- a composition for removing artificial metallic hair coloring material from hair comprising a sulphonated oleaginous material containing free sulphonic acid groups as the active hair color-removing constituent, an organic acid capable of forming soluble complexes or compounds with the various metals used in the dyeing art and a solvent mutually soluble in water and the sulphonated oleaginous material and organic acid of the class consisting of the polyhydric alcohols and derivatives thereof.
- a composition for removing artificial metallic hair coloring material from hair comprising a sulphonated higher fatty alcohol containing free sulphonic acid groups as the active hair colorremoving constituent, an organic acid capable of forming soluble complexes or compounds with the various metals used in the dyeing art and a solvent mutually soluble in water and the sulphonated alcohol and organic acid of the class consisting of the po-lyhydric alcohols and derivatives thereof.
- a composition for removing artificial metallic hair coloring material from hair comprising sulphonated castor oil containing free sulphonic acid groups as the active hair color-removing constituent, ethylene glycol and salicylic acid.
- a composition for removing artificial metallic hair coloring from living human hair comprising a sulphonated oil containing free sulphonic acid groups as the active hair color-removing con-.
- a remover for artificial metallic hair coloring material from living human hair comprising a major portion of sulphonated castor oil cantaming free sulphonic acid groups as the active hair color-removing constituent, a minor portion of ethylene glycol and a small portion of salicylic acid.
- a composition for removing artificial hair coloring material from hair comprising a sulphonated oleaginous material containing free sulphonic acid groups as the active hair colorremoving constituent and containing no free sulphuric acid.
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)
- Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Cosmetics (AREA)
Description
Patented Apr. 1, 1941' 2,286,970 miMovEa FOR ARTIFICIAL COLORS morn Abraham R. Goldfarb, New York, N. Y... assignor to Lawrence Richard Bruce Incorporated, a corporation of Connecticut v No Drawing.
Application March 22, 1937, Serial No. $2,295
Claims. (oil 167-88) This invention relates to color removers and more particularly to removers for the artificial colors of the metallic and vegetable dye type used in dyeing hair, and particularly living human hair.
In the art of dyeing hair, particularly human hair, containing artificial coloring material, it frequently is found desirable to remove the artificial coloring material .in the hair to. restore at least approximately its natural or preliminary color prior to a redyeing operation. Removers ,for some organic dyestuffs are known, butthese have not been available or satisfactory because of various reasons. Some emit odors upon being dissolved in a solvent and are highly objectionable in use, and moreover, have an injurious and deleterious effect on the hair or scalp or both.
Another drawback to the use of some of these known dye removers resides in the fact that they so aifect the hair structure that immediate redyeing of the hair is an impossibility, and a prolonged time interval, usually at least twentyfour hours, must elapse after the application of the hair dye remover before the hair'is in a suitable condition to be dyed again. In instances where the hair has been dyed with metallic dyes, metallic color restorers, and the like and some vegetable dyes, no satisfactory remover for these dyes have heretofore been developed, in so far as I am aware.
In accordance with my invention, I may produce a hair dye or hair color remover which is especially suitable for the removal of metallic dyes, metallic hair color restorers and of many vegetable dyes and which is free from the objections inherent in the known artificial color removers for hair. The color remover embodying my invention comprises a sulphonated oleaginous material, such as a sulphonated 011 or oily material, containing free sulphonic acid groups, and may be used alone or in aqueous solution; preferably, however, I use it in combination with an organic acid or a solvent which exhibits mutualsolvent capacity for water, the sulphonated oleaginous material and the organic acid or with both. The solvent, when used, appears to promote penetration and facilitate subsequent removal of the composition and dye; and the organic acid appears to improve penetration and promote the formation of a removable dye complex. This artificial color remover is particularly suitable for living human hair and is pears to properly condition the hair to render it immediately susceptible to recoloring or redyeing.
The sulphonated oleaginous material employed in my novel composition may suitably be a sulphonated vegetable oil, 'anima1 oil, or heavy mineral oil, or a sulphonated higher fatty alcohol, to
' which, after treatment with sulphuric acid'to effect sulphonation thereof, suflicient alkali such as sodium hydroxide or an organic base such as mono-, dior tri-ethanolamine has been added to neutralize substantially all of the free sulphuric acid. The amount of alkali which is added to the sulphonic acid derivative may be sufficient to neutralize not only all of the free sulphuric acid but some of the free sulphonic groups as well. In any event, it is essential that the sulphonated oleaginous material contain some free sulphonic acid groups and preferably all of them. Oleaginous material sulphonated to any desired extent may beused. I have found that oleaginous materials sulphonated to the extent of 6 to 15% to be highly eifective.
The oleaginous material subjected to sulphonation for use may be of any suitable character; thus it maybe a vegetable oil, such as the nondrying oils, castor oil, olive oil, and the like; the semi-drying oils, cottonseed oil, corn oil and the like; or the drying oils, linseed oil, perilla oil and the like; an animal oil, such as lard oil or commercial hydrogenated oils; or a mineral oil, preferably a heavy mineral oil distillate; or. higher fatty alcohols, such as lauryl, cetyl, myristyl and like fatty alcohols having 6 to 8 or more and preferably 12 or more carbon atoms in the carbon chain.
The organic acids employed in my novel composition are acids which are capable of forming Water solublecompounds or complexes with the highly effective in removing even the artificial variousmetals ordinarily used as mordants in dyeing hair, such as copper and iron. Thus for example, aromatic carboxylic acids suchas salicyclic acid; aliphatic carboxylic acids such as tartaric, lactic, citric, beta hydroxy butyric acid,
glycollic and malic; monoand di-baslc acidsderived from carbohydrates such as gluconlc and saccharic acids; aldehyde-hydroxy-acids such as glucuronic acid; or amino acetic acids such as glycocoll (glycine) and methyl glycocoll (sarcosine) and like acids may be used.
The common solvents employed in carrying out the invention are preferably organic solvents which are mutually soluble'in water and in the sulphonated oil or oily material and the organic acid embodied in my invention. Suitable solvents which may be used in carrying out the invention are glycerine, ethylene glycol and diethylene glycol; the alcohol ethers such as ethylene glycol mono-methyl ether. ethylene 81ycol mono-ethyl ether, ethylene glycol monobutyl ether, diethylene glycol mono-methyl ether, diethylene glycol mono-ethyl ether, diethylene glycol mono-butyl ether, and the like.
The following illustrative examples of compositions embodying my invention have been Under some conditions, as when the hair is dyed with a mixture of dyes of the metal and organic base types, the color or dye remover embodying my invention may remove substantially all of the metal dye but may not remove all of the organic dye and thus leave the hair with an undesirable shade. Even under these conditions the color remover leaves the hair in a condition for immediate retreatment with a dye for redyeing the hair to a desired shade or to modify the oil-shade. If desired, I may incorporate with my color remover a dye, suitably one of the wellknown progressive type and thus simultaneously redye the conditioned hair and thereby prevent the formation of ugly off-shades which may result from the removal of only part of a mixed dye.
It is readily apparent that other oleaginous materials as hereinbefore set forth may replace those employed in the formulas of these specific examples. Furthermore, theproportions of ingredients set forth'in the illustrative examples are not to be regarded as critical since the relative amounts of the ingredients may be varied within rather wide limits; or inert oils or water may be incorporated if desired. The best results have been obtained, however, by using a major part of the sulphonated oil or oily material, a minor part of common solvent and a small part of the organic acid. It is not desirable to use in excess of about of the organic acid since any great excess may cause an irritation of the scalp. Usually, satisfactory results have been oba,aao,o7o
thoroughly with some suitable rinsing solution and the hair is then shampooed in any conventional manner. Ordinary water. either cold or luke warm, will readily rinse the color removing composition and the dissolved color fromthe hair. I have found that hair treated with my novel composition in the manner described is,
either before or after drying, in excellent condition for treating with a dye solution for ,the purpose of coloring the hair to the desired shade.
' In some instances -of undue penetration of the dye into the-hair, the treatment above described is preferably repeated until all of the dye has been removed. Usually only a singletreatment is necessary.
I claim:
1. A composition for removing artificial metallic hair coloring material from hair comprising a sulphonated oleaginous material containing free sulphonic acid groups as the active hair colorremoving constituent and containing no free sulphuric acid.
2. A composition for removing artificial metallic hair coloring material from hair comprising sulphonated castor oil containing free sulphonic acid groups as the active hair color-removing constituent.
tained with organic acids in amounts varying from 1% to 10% and even higher and preferably from 2 to 5%. In some instances I have obtained satisfactory results in the removal of artificial colors by the use of the sulphonated oleaginous material of the character above set forth, either alone or with the described types of solvents in the absence oforganic acids.
In practicing my invention, the compostion is heated moderately, say to 100 F. to 125 F. or slightly higher, and is applied .in the heated state to the hair containing the artificial color either by the fingers or by brushing until the hair is thoroughly wetted. The air saturated with this composition is then warmed or heatedto a tolerable, high temperature in any suitable manner as by a heat lamp, hot towels, steamer or the like. This heating is continued for a suitable period, usually in the order of thirty to sixty minutes depending on the type of coloring material to be removed from the hair, the type and coarseness of the hair and other contributing factors.
After this heating operation, the hair is rinsed 3. A composition for removing artificial metallic hair coloring material from hair comprising a sulphonated oleaginous material containing free sulphonic acid groups asthe active hair colorremoving constituent and an organic acid capable of forming soluble complexes or compounds with the various metals used in the dyeing art.
4. A composition for removing artificial metallic hair coloring material from hair comprising a sulphonated oleaginous material containing free sulphonic acid groups as the active hair color-removing constituent, an organic acid capable of forming soluble complexes or compounds with the various metals used in the dyeing art and a solvent mutually soluble in water and the sulphonated oleaginous material and organic acid of the class consisting of the polyhydric alcohols and derivatives thereof.
5. A composition for removing artificial metallic hair coloring material from hair comprising a sulphonated higher fatty alcohol containing free sulphonic acid groups as the active hair colorremoving constituent, an organic acid capable of forming soluble complexes or compounds with the various metals used in the dyeing art and a solvent mutually soluble in water and the sulphonated alcohol and organic acid of the class consisting of the po-lyhydric alcohols and derivatives thereof.
6. A composition for removing artificial metallic hair coloring material from hair comprising sulphonated castor oil containing free sulphonic acid groups as the active hair color-removing constituent, ethylene glycol and salicylic acid.
7. A composition for removing artificial metallic hair coloring from living human hair comprising a sulphonated oil containing free sulphonic acid groups as the active hair color-removing con-.
used in the dyeing art and a minor portion of a I solvent mutually soluble in water and the sul-. phonated oleaginous material and. organic acid of the class consisting of the polyhydric alcohols and derivatives thereof.
I 9. A remover for artificial metallic hair coloring material from living human hair comprising a major portion of sulphonated castor oil cantaming free sulphonic acid groups as the active hair color-removing constituent, a minor portion of ethylene glycol and a small portion of salicylic acid.
10. A composition for removing artificial hair coloring material from hair comprising a sulphonated oleaginous material containing free sulphonic acid groups as the active hair colorremoving constituent and containing no free sulphuric acid.
ABRAHAM R. GOLDFARB.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US132295A US2236970A (en) | 1937-03-22 | 1937-03-22 | Remover for artificial colors from hair |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US132295A US2236970A (en) | 1937-03-22 | 1937-03-22 | Remover for artificial colors from hair |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2236970A true US2236970A (en) | 1941-04-01 |
Family
ID=22453351
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US132295A Expired - Lifetime US2236970A (en) | 1937-03-22 | 1937-03-22 | Remover for artificial colors from hair |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2236970A (en) |
Cited By (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2546898A (en) * | 1947-11-05 | 1951-03-27 | Mark Walter Vande | Deodorizing method |
| US2643211A (en) * | 1949-11-30 | 1953-06-23 | Rayette Inc | Hair color-rinse concentrate |
| US2739032A (en) * | 1953-03-30 | 1956-03-20 | William K Wilson | Iron-catalyzed decomposition of sodium chlorite |
| US2769748A (en) * | 1951-02-26 | 1956-11-06 | Lever Brothers Ltd | Thickened hair dyeing composition comprising polyhydroxyl compound and alkanolamine |
| US2825646A (en) * | 1954-09-27 | 1958-03-04 | Columbia Cellulose Company Ltd | Reducing the ash content of cellulose |
| US2826478A (en) * | 1955-07-19 | 1958-03-11 | Rohm & Haas | Method of bleaching mechanically-disintegrated wood pulp with hydrosulfite bleach containing an alkali metal citrate |
| US2898179A (en) * | 1955-06-01 | 1959-08-04 | Du Pont | Bleaching |
| US2965539A (en) * | 1957-01-15 | 1960-12-20 | Dow Chemical Co | Stabilization of pentachlorophenol solutions |
| US3035975A (en) * | 1957-06-24 | 1962-05-22 | Voigt Hans | Stable aqueous medicinal solutions |
| US3047460A (en) * | 1953-10-30 | 1962-07-31 | Riedel De Haen Ag | Fungicidal compositions and process for the preparation thereof |
| US3105798A (en) * | 1958-05-29 | 1963-10-01 | Procter & Gamble | Dentifrice composition |
| WO1998023247A1 (en) * | 1996-11-28 | 1998-06-04 | Wella Aktiengesellschaft | Agent for dyeing and decolorizing fibers |
| US6106579A (en) * | 1998-03-12 | 2000-08-22 | Wella Aktiengesellschaft | Compositions and methods for dyeing and safe decolorizing of fibers, especially hair, and multi-part kit for repeatedly changing dyed fiber color |
| US20110256081A1 (en) * | 2008-03-10 | 2011-10-20 | Jamie Anthony Hawkes | Hair Treatment Composition and Methods |
-
1937
- 1937-03-22 US US132295A patent/US2236970A/en not_active Expired - Lifetime
Cited By (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2546898A (en) * | 1947-11-05 | 1951-03-27 | Mark Walter Vande | Deodorizing method |
| US2643211A (en) * | 1949-11-30 | 1953-06-23 | Rayette Inc | Hair color-rinse concentrate |
| US2769748A (en) * | 1951-02-26 | 1956-11-06 | Lever Brothers Ltd | Thickened hair dyeing composition comprising polyhydroxyl compound and alkanolamine |
| US2739032A (en) * | 1953-03-30 | 1956-03-20 | William K Wilson | Iron-catalyzed decomposition of sodium chlorite |
| US3047460A (en) * | 1953-10-30 | 1962-07-31 | Riedel De Haen Ag | Fungicidal compositions and process for the preparation thereof |
| US2825646A (en) * | 1954-09-27 | 1958-03-04 | Columbia Cellulose Company Ltd | Reducing the ash content of cellulose |
| US2898179A (en) * | 1955-06-01 | 1959-08-04 | Du Pont | Bleaching |
| US2826478A (en) * | 1955-07-19 | 1958-03-11 | Rohm & Haas | Method of bleaching mechanically-disintegrated wood pulp with hydrosulfite bleach containing an alkali metal citrate |
| US2965539A (en) * | 1957-01-15 | 1960-12-20 | Dow Chemical Co | Stabilization of pentachlorophenol solutions |
| US3035975A (en) * | 1957-06-24 | 1962-05-22 | Voigt Hans | Stable aqueous medicinal solutions |
| US3105798A (en) * | 1958-05-29 | 1963-10-01 | Procter & Gamble | Dentifrice composition |
| WO1998023247A1 (en) * | 1996-11-28 | 1998-06-04 | Wella Aktiengesellschaft | Agent for dyeing and decolorizing fibers |
| US6106579A (en) * | 1998-03-12 | 2000-08-22 | Wella Aktiengesellschaft | Compositions and methods for dyeing and safe decolorizing of fibers, especially hair, and multi-part kit for repeatedly changing dyed fiber color |
| US20110256081A1 (en) * | 2008-03-10 | 2011-10-20 | Jamie Anthony Hawkes | Hair Treatment Composition and Methods |
| US8268013B2 (en) * | 2008-03-10 | 2012-09-18 | Perachem Limited | Hair treatment composition and methods |
| CN103315920A (en) * | 2008-03-10 | 2013-09-25 | 佩拉化学有限公司 | Hair treatment composition and methods |
| CN103315920B (en) * | 2008-03-10 | 2016-05-04 | 佩拉化学有限公司 | Hair coloring compositions and method |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US2236970A (en) | Remover for artificial colors from hair | |
| EP0022996B1 (en) | Process for the permanent reshaping of the hair | |
| JPS59500129A (en) | Sebum-inhibiting cosmetic agent containing long-chain alkanol and antioxidant | |
| USRE33845E (en) | Novel skin tanning composition | |
| DE3207612C2 (en) | Polyether derivatives and their use as emulsifiers | |
| WO1991011985A1 (en) | Oxidative hair dyeing agent made from a liquid dye carrier substance and composition in emulsion form containing an oxidizing agent, and oxidative hair-dyeing process | |
| EP0286774A1 (en) | Composition and process for permanently waving the hair | |
| DE3920984C2 (en) | ||
| DE2918422C2 (en) | Means for the mechanical removal of body hair | |
| US2655923A (en) | Method of shampooing and setting hair | |
| DE3030119A1 (en) | Hair-dye compsn. cream - contg. silicone oil or wax added to prim. thickener mixt. pref. sec. thickener and dispersant | |
| WO2021131868A1 (en) | Hair-dyeing method | |
| EP0653201B1 (en) | Agent for permanent hair waving and new hair keratine reducing cysteine glycerol esters | |
| US2340776A (en) | Topical epithelial anesthetic | |
| US2042698A (en) | Compositions foe dyeing hair | |
| JPS6084212A (en) | Method of dyeing fur or leather and composition therefor | |
| DE2454840B2 (en) | HAIR DETERGENT | |
| HU194731B (en) | Hair restorer | |
| CH307483A (en) | Hair treatment agents to enable the hair to retain the shape it has once given. | |
| DE958765C (en) | Soap-free preparation for coloring human hair | |
| DE19942350A1 (en) | Permanent hair styling or waving with short alkaline reduction treatment and longer-lasting acid reduction to give improved elasticity and spring | |
| JP2021102582A (en) | Hair dyeing method | |
| JPH10182373A (en) | Hair pretreating agent for dyeing hair and hair dyeing using the same | |
| DE534838C (en) | Prepared for rinsing hair after washing with alkaline substances | |
| DE608149C (en) | Fixatives for fragrances and volatile solvents |