US3148126A - Compositions suitable for hair curling - Google Patents
Compositions suitable for hair curling Download PDFInfo
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- US3148126A US3148126A US345701A US34570153A US3148126A US 3148126 A US3148126 A US 3148126A US 345701 A US345701 A US 345701A US 34570153 A US34570153 A US 34570153A US 3148126 A US3148126 A US 3148126A
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- hair
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- 210000004209 hair Anatomy 0.000 title description 36
- 239000000203 mixture Substances 0.000 title description 6
- 239000006210 lotion Substances 0.000 claims description 9
- -1 MERCAPTAN CARBOXYLIC ACID Chemical class 0.000 claims description 7
- 239000003513 alkali Substances 0.000 claims description 5
- 239000008365 aqueous carrier Substances 0.000 claims description 3
- 150000001875 compounds Chemical class 0.000 claims description 3
- 239000004615 ingredient Substances 0.000 claims description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 1
- 239000000243 solution Substances 0.000 description 29
- CWERGRDVMFNCDR-UHFFFAOYSA-N thioglycolic acid Chemical compound OC(=O)CS CWERGRDVMFNCDR-UHFFFAOYSA-N 0.000 description 14
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 11
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 9
- 235000011114 ammonium hydroxide Nutrition 0.000 description 9
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 6
- 239000000463 material Substances 0.000 description 5
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- 210000004761 scalp Anatomy 0.000 description 4
- 235000002639 sodium chloride Nutrition 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 239000012670 alkaline solution Substances 0.000 description 3
- 125000004432 carbon atom Chemical group C* 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 229940071127 thioglycolate Drugs 0.000 description 3
- CWERGRDVMFNCDR-UHFFFAOYSA-M thioglycolate(1-) Chemical compound [O-]C(=O)CS CWERGRDVMFNCDR-UHFFFAOYSA-M 0.000 description 3
- HXKKHQJGJAFBHI-UHFFFAOYSA-N 1-aminopropan-2-ol Chemical compound CC(O)CN HXKKHQJGJAFBHI-UHFFFAOYSA-N 0.000 description 2
- PMNLUUOXGOOLSP-UHFFFAOYSA-N 2-mercaptopropanoic acid Chemical compound CC(S)C(O)=O PMNLUUOXGOOLSP-UHFFFAOYSA-N 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- 241000208680 Hamamelis mollis Species 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- AYJRCSIUFZENHW-UHFFFAOYSA-L barium carbonate Chemical compound [Ba+2].[O-]C([O-])=O AYJRCSIUFZENHW-UHFFFAOYSA-L 0.000 description 2
- DKVNPHBNOWQYFE-UHFFFAOYSA-N carbamodithioic acid Chemical compound NC(S)=S DKVNPHBNOWQYFE-UHFFFAOYSA-N 0.000 description 2
- 230000002951 depilatory effect Effects 0.000 description 2
- 239000012990 dithiocarbamate Substances 0.000 description 2
- 238000004043 dyeing Methods 0.000 description 2
- 229940102253 isopropanolamine Drugs 0.000 description 2
- 230000009965 odorless effect Effects 0.000 description 2
- GNBVPFITFYNRCN-UHFFFAOYSA-M sodium thioglycolate Chemical compound [Na+].[O-]C(=O)CS GNBVPFITFYNRCN-UHFFFAOYSA-M 0.000 description 2
- 229940046307 sodium thioglycolate Drugs 0.000 description 2
- 239000001117 sulphuric acid Substances 0.000 description 2
- 235000011149 sulphuric acid Nutrition 0.000 description 2
- 229940118846 witch hazel Drugs 0.000 description 2
- BLFRQYKZFKYQLO-UHFFFAOYSA-N 4-aminobutan-1-ol Chemical compound NCCCCO BLFRQYKZFKYQLO-UHFFFAOYSA-N 0.000 description 1
- USFZMSVCRYTOJT-UHFFFAOYSA-N Ammonium acetate Chemical compound N.CC(O)=O USFZMSVCRYTOJT-UHFFFAOYSA-N 0.000 description 1
- 239000005695 Ammonium acetate Substances 0.000 description 1
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical class S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 1
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 description 1
- CTKINSOISVBQLD-UHFFFAOYSA-N Glycidol Chemical compound OCC1CO1 CTKINSOISVBQLD-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- 206010028813 Nausea Diseases 0.000 description 1
- 235000008331 Pinus X rigitaeda Nutrition 0.000 description 1
- 235000011613 Pinus brutia Nutrition 0.000 description 1
- 241000018646 Pinus brutia Species 0.000 description 1
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 1
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical group CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 description 1
- GNVMUORYQLCPJZ-UHFFFAOYSA-M Thiocarbamate Chemical compound NC([S-])=O GNVMUORYQLCPJZ-UHFFFAOYSA-M 0.000 description 1
- 241001416177 Vicugna pacos Species 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 235000001014 amino acid Nutrition 0.000 description 1
- 150000001413 amino acids Chemical class 0.000 description 1
- YNNGZCVDIREDDK-UHFFFAOYSA-N aminocarbamodithioic acid Chemical compound NNC(S)=S YNNGZCVDIREDDK-UHFFFAOYSA-N 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 229940043376 ammonium acetate Drugs 0.000 description 1
- 235000019257 ammonium acetate Nutrition 0.000 description 1
- 239000000908 ammonium hydroxide Substances 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 230000003796 beauty Effects 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 235000018417 cysteine Nutrition 0.000 description 1
- XUJNEKJLAYXESH-UHFFFAOYSA-N cysteine Natural products SCC(N)C(O)=O XUJNEKJLAYXESH-UHFFFAOYSA-N 0.000 description 1
- 230000006378 damage Effects 0.000 description 1
- 230000002939 deleterious effect Effects 0.000 description 1
- 229910001882 dioxygen Inorganic materials 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- DOGJSOZYUGJVKS-UHFFFAOYSA-N glyceryl monothioglycolate Chemical compound OCC(O)COC(=O)CS DOGJSOZYUGJVKS-UHFFFAOYSA-N 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- 239000011147 inorganic material Substances 0.000 description 1
- 229910052945 inorganic sulfide Inorganic materials 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 150000007530 organic bases Chemical class 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 230000000135 prohibitive effect Effects 0.000 description 1
- 229960004063 propylene glycol Drugs 0.000 description 1
- 235000013772 propylene glycol Nutrition 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- JBJWASZNUJCEKT-UHFFFAOYSA-M sodium;hydroxide;hydrate Chemical compound O.[OH-].[Na+] JBJWASZNUJCEKT-UHFFFAOYSA-M 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
- 125000003396 thiol group Chemical group [H]S* 0.000 description 1
- NBOMNTLFRHMDEZ-UHFFFAOYSA-N thiosalicylic acid Chemical compound OC(=O)C1=CC=CC=C1S NBOMNTLFRHMDEZ-UHFFFAOYSA-N 0.000 description 1
- 229940103494 thiosalicylic acid Drugs 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- 210000002268 wool Anatomy 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q5/00—Preparations for care of the hair
- A61Q5/04—Preparations for permanent waving or straightening the hair
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- 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
Definitions
- compositions suitable for hair curling and is herein disclosed in some detail as embodied in compositions suitable for cold hair waving.
- This application is a division of my application Serial No. 437,628, filed April 4, 1942, now abandoned, which latter is in part a continuation of my prior application Serial No. 383,204, filed March 1'3, 1941, now Patent No. 2,350,178, of May 30, 1944.
- a curling solution which is highly effective in the cold, is harmless, is economical to prepare, is safe in unskilled hands, is so nearly odorless that its odor is easily covered up, leaves no toxic or otherwise objectionable residue, does not injure the hands of an operator or the scalp of a person whose hair is being curled, and does not act as a depilatory.
- the solution is in every way suit able to put into the hands of the average housewife. Modified solutions may be used hot, if weaker, or may be useful when speed is desired.
- a more rapid procedure was to wet the rolled-up hair with the same solution, leave for fifteen minutes or more, depending on the texture and condition of the hair, or, for bleached or dyed hair, ten minutes, and wet with a solution made by mixing 500 cc. of 20 volume hydrogen peroxide with 500 cc. water and 30 grams tartaric acid. This neutralizes the alkalinity of the ammonia-containing solution and incidentally raises the hair to 125 F.
- Evaporation of the water from the chemicals used appears to be an effective agent in this process.
- the oxygen of the air seems to convert the thioglycolate to a dithiodiglycolate which is inert and comparatively odorless.
- This formula was effective on fine hair (which yields slowly to treatment), as well as on bleached, dyed and coarse hair, the time varying from five to thirty minutes, when cold.
- alkali metal salts give a tighter curl on some types of hair.
- Solutions with a pH of 9.02 have proved the most satisfactory compromise solution for all round use, considering fineness of hair, temperature, time and other considerations of beauty parlor practice.
- One such solution was 7 grams thioglycolic acid 100 cc.
- Water Sodium or potassium hydroxide solution to make pH 8, then 26 B. aqua ammonia to make pH 9.9, then dilute to cc.
- isopropanolamine When isopropanolamine was substituted for the monoethanolamine, it yielded a parallel product of about equal utility. That product may be called isopropanolammonium dithiocarbamate. It was possible to use ammonium dithiocarbamate made in the same way, by using an excess of ammonium hydroxide, although its odor made it less useful.
- N-oxyethylthioglycolamide was made by dehydrating a mixture of monoethanolamine and thioglycolic acid. The mixture was heated at about 140 C. at a pressure of 15 to 22 mm. until the proper computed amount of water was removed and collected. The resulting product was ready for immediate use, when in proper solution.
- Propylene oxide substituted for the ethylene oxide yielded the corresponding propyleneglycol product which was about equally useful in hair curling.
- Glycidol when substituted for the ethylene oxide yielded the corresponding glyceryl monothioglycolate, which also proved useful in hair curling.
- Monothioglycerine and thiosalicylic acid were found to be usable in suitable concentrations though inferior to most of the other materials named above.
- the material was hung up and dried. It dried with the crease ironed in at one line, but dried flat elsewhere where treated and the crease was permanent. The untreated area wrinkled. The color was slightly affected,
- the process of giving permanent shape to hair which comprises arranging'the hair in the desired form and treating it with an alkaline solution containing an alkanolamide of an aliphatic mercaptan carboxylic acid of not more than three carbon atoms, the amount of said mercaptan compound by weight being from about 1% to 15%, said solution having a pH of from about 7 to about 9.5, and thereafter. eliminating such solution from the hair in order to set the latter.
- the process of giving permanent shape to hair which comprises arranging the hair in the desired form and treating it with an alkaline solution of N-oxyethylthioglycolamide, the amount of said N-oxyethylthioglycolamide by weight being from about 1% to 15%, said solution having a pH of from about 7 to about 9.5, andthereafter eliminating such solution from the hair in order to set the latter.
- a hair-waving lotion having as its principal ingredient an N-alkanolamide of an aliphatic mercaptan carboxylic acid of not more than three carbon atoms, the amount of said mercaptan compound by weight being from about 1 to 15 said lotion containing free alkali to give a pH of from about 7 to about 9.5 and containing also an aqueous carrier for said compound and said alkali, said lotion being useful to impart a permanent wave to hair in the cold.
- a hair-waving lotion having as its principal ingredient N-oxyethylthioglycolamide, the amount of said N- oxyethylthioglycolamide by weight being from about 1 to 15%, said lotion containing free alkali to give a pH of from about 7 to about 9.5 and containing also an aqueous carrier for said N-oxyethylthioglycolamide and said alkali, said lotion being useful to impart a permanent wave to hair in the cold.
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- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Birds (AREA)
- Epidemiology (AREA)
- Cosmetics (AREA)
Description
United States Patent 3,148,126 COMPOSITIONS SUITABLE FOR HAIR CURLING Harry Martin, Monroe, N.Y., assignor, by mesne assignments, to Permanent Hair Waving Corporation, Norfolk, Va., a corporation of Virginia No Drawing. Original application Apr. 4, 1942, Ser. No. 437,628. Divided and this application Mar. 30, 1953, Ser. No. 345,701
4 Claims. (Cl. 16787.1)
This invention relates to compositions suitable for hair curling, and is herein disclosed in some detail as embodied in compositions suitable for cold hair waving. This application is a division of my application Serial No. 437,628, filed April 4, 1942, now abandoned, which latter is in part a continuation of my prior application Serial No. 383,204, filed March 1'3, 1941, now Patent No. 2,350,178, of May 30, 1944.
It has been found possible in the past, if dangers and unpleasantness were ignored, to elfect the cold waving of hair with inorganic sulfides or hydrosulfides, but some people seem to have been fatally poisoned by solutions of those inorganic materials, and, moreover, the odor of the substances used was highly oflensive and nauseous.
It hast been hitherto proposed to use the hydrochloride of the sulfur-bearing amino acid cysteine, but that is commercially prohibitive and was used at pH of about 11, which irritated the operators hands and the scalp carrying the treated hair.
Other substances have been tried, but had to be so strongly alkaline when used that they stung the hands of the operator or the scalp of the person whose hair was being curled, and for that reason, were practically worthless for most purposes.
According to the present invention, the foregoing and other difficulties are overcome, and a curling solution is provided which is highly effective in the cold, is harmless, is economical to prepare, is safe in unskilled hands, is so nearly odorless that its odor is easily covered up, leaves no toxic or otherwise objectionable residue, does not injure the hands of an operator or the scalp of a person whose hair is being curled, and does not act as a depilatory. Moreover, the solution is in every way suit able to put into the hands of the average housewife. Modified solutions may be used hot, if weaker, or may be useful when speed is desired.
In one form of the invention, ten grams of sodium thioglycolate were dissolved in 100 cc. of water, making a solution of pH 6 to 7, and applied to the hair wound on a rod at room temperature. In the course of an hour to three hours, the still wound hair was washed with warm water, say below 125 F. The hair appeared unharmed and waved permanently to the wound shape.
The same solution, in the hands of a skilled operator, with the further addition of 15 cc. of 26 B aqua ammonia, making a solution of pH 11.6 waved the hair in one and one-half to two hours, and was washed out the same way.
A more rapid procedure was to wet the rolled-up hair with the same solution, leave for fifteen minutes or more, depending on the texture and condition of the hair, or, for bleached or dyed hair, ten minutes, and wet with a solution made by mixing 500 cc. of 20 volume hydrogen peroxide with 500 cc. water and 30 grams tartaric acid. This neutralizes the alkalinity of the ammonia-containing solution and incidentally raises the hair to 125 F.
Evaporation of the water from the chemicals used appears to be an effective agent in this process. The oxygen of the air seems to convert the thioglycolate to a dithiodiglycolate which is inert and comparatively odorless.
It was found that oxygen gas delivered under a helmet covering the scalp was highly effective in arresting action 3,148,126 Patented Sept. 8, 1964 of the thioglycolate and destroying its odor and giving the best interior curl.
One solution deodorized by witch-hazel was well adapted to professional use, as follows:
10 grams thioglycolic acid 7 grams sodium hydroxide 20 cc. 26 B. aqua ammonia 100 cc. water or witch-hazel 2 drops synthetic oil (to give a positive odor) of pine.
This formula was effective on fine hair (which yields slowly to treatment), as well as on bleached, dyed and coarse hair, the time varying from five to thirty minutes, when cold.
For domestic use by unskilled persons modified formulas were the best, using 4% to 10% of a soluble thioglycolate and a pH between 7 and 9.5. Above pH 10, a depilatory action shows itself in partial or incipient destruction of the hair fibre. Occasionally a 3% solution is advisable, and as high as 15% is usable by a skilled operator under some conditions.
It is usually most satisfactory to make the solution alkaline by aqua ammonia, but alkali metal salts give a tighter curl on some types of hair. Many common salts, even sodium chloride, sodium sulphate, and ammonium acetate, when present, exert definitely deleterious effects.
Ofter the best effects are obtained by adding an organic base to replace part of the sodium as:
10 grams thioglycolic acid 3 grams monoethanol amine 1 gram sodium thioglycolate were dissolved in less than 100 cc. water, 26 B. aqua ammonia was added to make pH 8.5 and water added to make 100 cc.
Another material was made with 6.5 grams thioglycolic acid cc. water Monoethanolamine to make pH 7 Aqua ammonia to make pH 9.05 Water to make cc.
Solutions with a pH of 9.02 have proved the most satisfactory compromise solution for all round use, considering fineness of hair, temperature, time and other considerations of beauty parlor practice. One such solution was 7 grams thioglycolic acid 100 cc. Water Sodium or potassium hydroxide solution to make pH 8, then 26 B. aqua ammonia to make pH 9.9, then dilute to cc.
A 1% alkaline solution of the thioglycolic acid curled hair at 212 F.
Other acids and salts containing not more than three carbon atoms in the acid radical were usable. Thus 8.5 grams thiolactic acid 90 cc. water Monoethanolamine added to make pH 8 Then 26 B. aqua ammonia to make pH 8.5 diluted to The resulting dithiocarbamate in suitable solution, curled hair rapidly and safely and was easily washed out, to fix the curl. As little as a 4% solution was found useful especially in the cold. The product may be called a solution of monoethanolarnmonium-N-oxyethyldithiocarbamate. It was stable over a period of some weeks.
When isopropanolamine was substituted for the monoethanolamine, it yielded a parallel product of about equal utility. That product may be called isopropanolammonium dithiocarbamate. It was possible to use ammonium dithiocarbamate made in the same way, by using an excess of ammonium hydroxide, although its odor made it less useful.
Other useful results were obtained by producing amides and treating hair with them in solution, thus avoiding any uncertainty or difiiculty arising from the possible instability of the thiocarbamate.
N-oxyethylthioglycolamide was made by dehydrating a mixture of monoethanolamine and thioglycolic acid. The mixture was heated at about 140 C. at a pressure of 15 to 22 mm. until the proper computed amount of water was removed and collected. The resulting product was ready for immediate use, when in proper solution.
Isopropanolamine substitued for the monoethanolamine under the same conditions, yielded a corresponding product similarly useful. The product was N-oxypropyldithioglyeolamide.
When butanolamine was substituted for-the monoethanolarnine under the same conditions, it yielded a corre- 3 To thioglycolic acid, containing about a fraction .of
1% of sulphuric acid, was added slowly with intermittent cooling, a slight excess of ethylene oxide yielding a viscous liquid, ready to use in hair curling when in suitable solution after removal of the sulphuric acid as by barium carbonate. The product in solution was ethyleneglycolmonothioglycolate.
Propylene oxide substituted for the ethylene oxide yielded the corresponding propyleneglycol product which was about equally useful in hair curling. Glycidol when substituted for the ethylene oxide yielded the corresponding glyceryl monothioglycolate, which also proved useful in hair curling.
Monothioglycerine and thiosalicylic acid were found to be usable in suitable concentrations though inferior to most of the other materials named above.
It was found that many of these materials were effective on the other animal fibres and were useful in treating woolen textiles, for example, to make them crease resistant and make them hold creases, as for instance in mens trousers.
A pink flannel made by Botany Worsted Mills 404/ 1068/ 13444 E. B. was wet with a 4% solution of monoethanolammonium-N-oxyethyldithiocarbamate with aqua ammonia added to make a pH of about 9, and heated with a crease for to seconds to 200 F. on a flat surface with an electric iron, washed with very dilute acetic acid and then with very dilute hydrogen peroxide.
The material was hung up and dried. It dried with the crease ironed in at one line, but dried flat elsewhere where treated and the crease was permanent. The untreated area wrinkled. The color was slightly affected,
but this may be allowedfor in dyeing. The feel of the treated portion was improved to that of a much more expensive flannel;
A purple soft fine womans wear wool with a tendency to crepe wh'n wetted made by the same company 114/ /6649 was similarly treated with the same solution, at a temperature of about 180 F. with a crease. The color was slightly altered, which could be allowed for in the dyeing. The material retained its crease where treated and dried flat where treated, but became crepelike elsewhere.
A blue mans worsted cloth, like a summer alpaca 48/ 1/ 179 made by the same people was similarly treated at F. The crease was permanent and the treated area remained flat.
It will be noted that most of the named compounds contain both a hydroxyl and a mercapto group and contain an organic radical either in the acid or the basic element.
Reference is made to the companion application Serial No. 276,883, filed March 15, 1952, now US. Patent No. 2,876,781 from which application claims have been transferred.
Having thus described my invention and illustrated its use, what I claim as new and desire to secure by Letters Patent is:
1. The process of giving permanent shape to hair which comprises arranging'the hair in the desired form and treating it with an alkaline solution containing an alkanolamide of an aliphatic mercaptan carboxylic acid of not more than three carbon atoms, the amount of said mercaptan compound by weight being from about 1% to 15%, said solution having a pH of from about 7 to about 9.5, and thereafter. eliminating such solution from the hair in order to set the latter.
2. The process of giving permanent shape to hair which comprises arranging the hair in the desired form and treating it with an alkaline solution of N-oxyethylthioglycolamide, the amount of said N-oxyethylthioglycolamide by weight being from about 1% to 15%, said solution having a pH of from about 7 to about 9.5, andthereafter eliminating such solution from the hair in order to set the latter.
3. A hair-waving lotion having as its principal ingredient an N-alkanolamide of an aliphatic mercaptan carboxylic acid of not more than three carbon atoms, the amount of said mercaptan compound by weight being from about 1 to 15 said lotion containing free alkali to give a pH of from about 7 to about 9.5 and containing also an aqueous carrier for said compound and said alkali, said lotion being useful to impart a permanent wave to hair in the cold.
4. A hair-waving lotion having as its principal ingredient N-oxyethylthioglycolamide, the amount of said N- oxyethylthioglycolamide by weight being from about 1 to 15%, said lotion containing free alkali to give a pH of from about 7 to about 9.5 and containing also an aqueous carrier for said N-oxyethylthioglycolamide and said alkali, said lotion being useful to impart a permanent wave to hair in the cold.
References Cited in the file of this patent UNITED STATES PATENTS 2,736,323 McDonough Feb. 28, 1956
Claims (1)
- 3. A HAIR-WAVING LOTION HAVING AS ITS PRINCIPAL INGREDIENT AN N-ALKANOLAMIDE OF AN ALIPHATIC MERCAPTAN CARBOXYLIC ACID OF NOT MORE THAN THREE CARBON ATOMS, THE AMOUNT OF SAID MERCAPTAN COMPOUND BY WEIGHT BEING FROM ABOUT 1 TO 15%, SAID LOTION CONTAINING FREE ALKALI TO GIVE A PH OF FROM ABOUT 7 TO ABOUT 9.5 AND CONTAINING ALSO AN AQUEOUS CARRIER FOR SAID COMPOUND AND SAID ALKALI, SAID LOTION BEING USEFUL TO IMPART A PERMANENT WAVE TO HAIR IN THE COLD.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US345701A US3148126A (en) | 1942-04-04 | 1953-03-30 | Compositions suitable for hair curling |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US43762842A | 1942-04-04 | 1942-04-04 | |
| US345701A US3148126A (en) | 1942-04-04 | 1953-03-30 | Compositions suitable for hair curling |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US3148126A true US3148126A (en) | 1964-09-08 |
Family
ID=26994520
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US345701A Expired - Lifetime US3148126A (en) | 1942-04-04 | 1953-03-30 | Compositions suitable for hair curling |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US3148126A (en) |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4192863A (en) * | 1964-06-12 | 1980-03-11 | Tokuzo Kondo | Completely one-step permanent wave solution and a method for using the same |
| US4832948A (en) * | 1985-09-10 | 1989-05-23 | Tokuzo Kondo | Permanent wave solution |
| US5041286A (en) * | 1988-07-26 | 1991-08-20 | Yasmin Products Pty. Limited | Process for reconfiguring keratin fibre |
| US5091573A (en) * | 1990-08-11 | 1992-02-25 | Rohm And Haas Company | Thiol-terminated hydroxyamides |
| US5247125A (en) * | 1990-08-11 | 1993-09-21 | Rohm And Haas Company | Thiol-terminated hydroxyamides |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2736323A (en) * | 1949-08-13 | 1956-02-28 | Tide Water Patent Dev Company | Permanent waving solutions and method |
-
1953
- 1953-03-30 US US345701A patent/US3148126A/en not_active Expired - Lifetime
Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2736323A (en) * | 1949-08-13 | 1956-02-28 | Tide Water Patent Dev Company | Permanent waving solutions and method |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4192863A (en) * | 1964-06-12 | 1980-03-11 | Tokuzo Kondo | Completely one-step permanent wave solution and a method for using the same |
| US4832948A (en) * | 1985-09-10 | 1989-05-23 | Tokuzo Kondo | Permanent wave solution |
| US5041286A (en) * | 1988-07-26 | 1991-08-20 | Yasmin Products Pty. Limited | Process for reconfiguring keratin fibre |
| US5091573A (en) * | 1990-08-11 | 1992-02-25 | Rohm And Haas Company | Thiol-terminated hydroxyamides |
| US5247125A (en) * | 1990-08-11 | 1993-09-21 | Rohm And Haas Company | Thiol-terminated hydroxyamides |
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