US3063908A - Process for permanent deformation of hair - Google Patents
Process for permanent deformation of hair Download PDFInfo
- Publication number
- US3063908A US3063908A US769097A US76909758A US3063908A US 3063908 A US3063908 A US 3063908A US 769097 A US769097 A US 769097A US 76909758 A US76909758 A US 76909758A US 3063908 A US3063908 A US 3063908A
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- Prior art keywords
- solution
- hair
- acid
- amide
- permanent deformation
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- 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
-
- 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
Definitions
- the object of the present invention is to provide a process utilizing mercaptoalkanoic amides for obtaining plasticization of the keratin of live hair or of similar fibers, which does not possess the aforesaid disadvantages.
- a process for the permanent deformation of live human hair or other keratinous fibers which comprises impregnating the hair or fibers with a freshly prepared aqueous solution, obtained by adding to an aqueous alkaline stocksolution of a primary or secondary mercaptoalkanoic acid amide an acid or acidic buffer composition, in a quantity sufficient to ensure a pH value of 5 to 7.5 in the resulting solution, constraining the hair or fibers in a desired configuration, and thereafter fixing them in a known manner while in said configuration.
- the aqueous alkaline stock-solution has a pH above 8 and the hair impregnating solution has a pH of about 7.
- the acid or acidic buffer composition may be in the form of an aqueous solution or a powder which will dissolve in the amide solution.
- Another object of the present invention is a hair-waving kit for use in accordance with the above-mentioned process, comprising two separate compositions to be atent O mixed at the time of use, one of which is an aqueous alkaline stock-solution of a primary or secondary mercaptoalkanoic acid amide and the other one is a quantity of an acid or acidic buffer composition which is suflicient to impart the resulting mixture a pH value of 5 to 7.5.
- R is a hydrogen atom or an alkyl group containing not more than- 4 carbon atoms
- R is a hydrogen atom or an alkyl group containing not more than 4 carbon atoms
- R" is a hydrogen atom or an alkyl or hydroxyalkyl group containing not more than 4 carbon atoms.
- the concentration of amide in the amide solution should be in general from 0.5 to 1.5 molar and the desired alkalinity of the solution may be obtained by using weak bases, such as ammonia or organic bases (e.g. mono-, dior triethanolamine).
- weak bases such as ammonia or organic bases (e.g. mono-, dior triethanolamine).
- the acid or acidic buffer composition may contain weak acids such as acetic acid or lactic acid, or salts possessing marked buffering properties and giving acid solutions on hydrolysis such as di-hydrogen phosphates, acid citrates and acid phthalates, of potassium, sodium and ammonium.
- the quantity of acidic compound to be used in the composition is calculated as a function of the pH and of the quantity of base introduced into the first solution, so that, when the two componentshave been mix-ed, the pH of the final solution is 5 to 7.5 preferably 7.
- the two compositions are mixed immediately prior to application of the mixture to the hair.
- the final mixture provides a permanent waving liquid which will act in acidic or neutral medium and which is not harmful to the keratin of .the hair and at the same time contains only very small quantities of hydrogen sulphide.
- Example I 100 cc. of a 9.9% aqueous solution of mercaptoacetamide (SHCH -CO-NH adjusted to a pH of 8.5 with ammonia (about 11 g./l. of NH were neutralized at the time of use with 10 cc. of a citric acid solution (390 g./ 1.). The resultant mixture had a pH of 6.8 to 6.9.
- Human hair was impregnated with this solution, Wound on curlers and left in contact with the solution for 15 to 25 minutes at room temperature, or from 8 to 12 minutes with heating at about C. by means of any suitable device. The hair was then rinsed and treated with an oxidizing solution.
- the wave obtained was of attractive appearance and completely resistant to washing and moisture.
- the hands of the operator and the scalp of the treated person remained unaffected.
- Example II An 8% aqueous solution of mercaptoacetamide was brought to pH 9.0 with ammonia. cc. of this solution were neutralized at the time of use with 8 g. of ammonium (ii-hydrogen orthophosphate. The resultant solution had a pH of 6 .6. to 6.7 and it was applied as described in Example I and with similar results.
- Example III 100 cc. of a 5.5% aqueous solution of N-methyl mercaptoacetamide (SHCH CONHCH containing 3% of ammonium di-hydrogen orthophosphate were brought to pH 8.4 with ammonia. At the time of use, 100 cc. of a lactic acid solution (520 g./l.) were added thereto, giving the resultant solution a pH of 6.2. This solution was used as described in Example I and gave similar results.
- SHCH CONHCH containing 3% of ammonium di-hydrogen orthophosphate were brought to pH 8.4 with ammonia.
- 100 cc. of a lactic acid solution 520 g./l.
- Example I An 11.5% aqueous solution of a-mercaptopropionamide was brought to pH 8.6 with ammonia. At the time of use, 100 cc. of this solution were neutralized with 10 cc. of a solution containing 300 g./l. of citric acid and 550 g./l. of sodium di-hydrogen orthophosphate. The pH of the resultant solution was 6.8 and it was used under the same conditions and gave similar results as described in Example 1.
- Example V 100 cc. of a 9.9% aqueous solution of mercaptoacetamide containing sufiicient ammonia to have a pH of 8.5 (about 11 g./l. of NH were neutralized at the time of use by the addition of about 3.9 g. of citric acid in powder form. The mixture was stirred to efiect complete dissolution of citric acid. The resultant solution had a pH of 6.8 to 6.9. This solution was applied as described in Example I and gave similar results.
- a process for the permanent deformation of live human hair which comprises:
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- Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
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Description
waving compositions.
United States 3,063,908 PROCESS FOR PERMANENT DEFORMATION OF HAIR Gregoire Kalopissis, Paris, France, assignor to LOreal, Paris, France No D rawing. Filed Oct. 23, 1958, Ser. No. 769,097 Claims priority, application France May 29, 1958 4 Claims. (Cl. 167--87.1)
from a theoretical standpoint serious drawbacks are encountered, as a result of which the mercaptoa mides cannot readily be commercialized in the form of hair When the aforementioned amides are employed in alkaline 'media for-hair waving, e.g. from pH 8 to 9.5, the prepared solutions, which areof the order of 0.5 to 1.5 molar, appear to be substantially stable and do not liberate any hydrogen sulphide. On the other hand, within such a pH range, it is usually impossible for the operator to perform more than three permanent waving operations with bare hands without suffering serious injury to the hands. As a rule, these alkaline amide solutions also produce itching and irritation of the scalp of the treated persons, and lesions may be produced which in some cases may be fairly serious.
When the same amides are employed in the same concentration in solutions of lower pH values ranging, for example, from 5 to 7.5, the resulting solutions are unstable and very rapidly liberate considerable quantities of hydrogen sulphide, which render them unusuable. Moreover, by reason of the nauseous odour and the toxicity of hydrogen sulphide, in most countries the use of hair waving compositions containing this compound is prohibited, or the concentration in which it may be present in them is limited by law. However, in this lower pH range, the injurious action of the aforesaid solutions on the hands of the operator is greatly reduced and they do not produce any itching or irritation of the scalp of treated persons.
The object of the present invention is to provide a process utilizing mercaptoalkanoic amides for obtaining plasticization of the keratin of live hair or of similar fibers, which does not possess the aforesaid disadvantages.
According to the present invention there is provided a process for the permanent deformation of live human hair or other keratinous fibers which comprises impregnating the hair or fibers with a freshly prepared aqueous solution, obtained by adding to an aqueous alkaline stocksolution of a primary or secondary mercaptoalkanoic acid amide an acid or acidic buffer composition, in a quantity sufficient to ensure a pH value of 5 to 7.5 in the resulting solution, constraining the hair or fibers in a desired configuration, and thereafter fixing them in a known manner while in said configuration. Preferably the aqueous alkaline stock-solution has a pH above 8 and the hair impregnating solution has a pH of about 7. The acid or acidic buffer composition may be in the form of an aqueous solution or a powder which will dissolve in the amide solution.
Another object of the present invention is a hair-waving kit for use in accordance with the above-mentioned process, comprising two separate compositions to be atent O mixed at the time of use, one of which is an aqueous alkaline stock-solution of a primary or secondary mercaptoalkanoic acid amide and the other one is a quantity of an acid or acidic buffer composition which is suflicient to impart the resulting mixture a pH value of 5 to 7.5.
The amides which may be used according to the invention conform to the general formula:
wherein R is a hydrogen atom or an alkyl group containing not more than- 4 carbon atoms, R is a hydrogen atom or an alkyl group containing not more than 4 carbon atoms and R" is a hydrogen atom or an alkyl or hydroxyalkyl group containing not more than 4 carbon atoms.
, i The concentration of amide in the amide solution should be in general from 0.5 to 1.5 molar and the desired alkalinity of the solution may be obtained by using weak bases, such as ammonia or organic bases (e.g. mono-, dior triethanolamine).
The acid or acidic buffer composition may contain weak acids such as acetic acid or lactic acid, or salts possessing marked buffering properties and giving acid solutions on hydrolysis such as di-hydrogen phosphates, acid citrates and acid phthalates, of potassium, sodium and ammonium. The quantity of acidic compound to be used in the composition is calculated as a function of the pH and of the quantity of base introduced into the first solution, so that, when the two componentshave been mix-ed, the pH of the final solution is 5 to 7.5 preferably 7.
The two compositions are mixed immediately prior to application of the mixture to the hair. The final mixture provides a permanent waving liquid which will act in acidic or neutral medium and which is not harmful to the keratin of .the hair and at the same time contains only very small quantities of hydrogen sulphide.
It is of course within the ambit of the present invention to incorporate into the final solution additional agents intended for the treatment and grooming of the hair, which agents may be added to one or both of the components of the final solution before mixing them.
The following examples will serve to illustrate the invention. All percentages are by weight.
Example I 100 cc. of a 9.9% aqueous solution of mercaptoacetamide (SHCH -CO-NH adjusted to a pH of 8.5 with ammonia (about 11 g./l. of NH were neutralized at the time of use with 10 cc. of a citric acid solution (390 g./ 1.). The resultant mixture had a pH of 6.8 to 6.9.
Human hair was impregnated with this solution, Wound on curlers and left in contact with the solution for 15 to 25 minutes at room temperature, or from 8 to 12 minutes with heating at about C. by means of any suitable device. The hair was then rinsed and treated with an oxidizing solution.
The wave obtained was of attractive appearance and completely resistant to washing and moisture. The hands of the operator and the scalp of the treated person remained unaffected.
Example II An 8% aqueous solution of mercaptoacetamide was brought to pH 9.0 with ammonia. cc. of this solution were neutralized at the time of use with 8 g. of ammonium (ii-hydrogen orthophosphate. The resultant solution had a pH of 6 .6. to 6.7 and it was applied as described in Example I and with similar results.
Example III 100 cc. of a 5.5% aqueous solution of N-methyl mercaptoacetamide (SHCH CONHCH containing 3% of ammonium di-hydrogen orthophosphate were brought to pH 8.4 with ammonia. At the time of use, 100 cc. of a lactic acid solution (520 g./l.) were added thereto, giving the resultant solution a pH of 6.2. This solution was used as described in Example I and gave similar results.
Example I An 11.5% aqueous solution of a-mercaptopropionamide was brought to pH 8.6 with ammonia. At the time of use, 100 cc. of this solution were neutralized with 10 cc. of a solution containing 300 g./l. of citric acid and 550 g./l. of sodium di-hydrogen orthophosphate. The pH of the resultant solution was 6.8 and it was used under the same conditions and gave similar results as described in Example 1.
Example V 100 cc. of a 9.9% aqueous solution of mercaptoacetamide containing sufiicient ammonia to have a pH of 8.5 (about 11 g./l. of NH were neutralized at the time of use by the addition of about 3.9 g. of citric acid in powder form. The mixture was stirred to efiect complete dissolution of citric acid. The resultant solution had a pH of 6.8 to 6.9. This solution was applied as described in Example I and gave similar results.
What I claim is:
1. A process for the permanent deformation of live human hair, which comprises:
(a) preparing a stock solution having a pH of between 8 and 9.5, for storage purposes, of an aqueous solution of an amide of mercapto alkanoic acid of the general formula in which R is selected from the group consisting of hydrogen atoms and those alkyl groups having at most 3 carbon atoms, R is selected from the group consisting of a hydrogen atom and those alkyl groups having at most 3 carbon atoms, and R" is selected from the group consisting of a hydrogen atom, alkyl and hydroxyl alkyl groups having at most 3 carbon atoms,
(b) the step of adding a substance having an acid reaction selected from the group consisting of organic acid, their acid salts and acid salts of inorganic acids in a quantity suflicient to bring the pH of the mixture to a value of between 5 and 7.5 at the time of application to the hair,
(a) constraining the hair in a desired configuration,
(d) applying said solution having a pH of between 5 and 7.5 to the hair,
(e) fixing the hair in said configuration by means of oxidation.
2. A process as claimed in claim 1, in which the amide of the mercapto alkanoic acid is mercaptoacetamide.
3. A process as claimed in claim 1, in which the amide is N-rnethyl-mercaptoacetamide.
4. A process as claimed in claim 1, in which the amide of the mercapto alkanoic acid is alpha-mercaptopropionamide.
Re er n es Cit in. the fil of t is pa UNITED STATES PATENTS OTHER REFERENCES Valko: LS. Cos. Chemists, 3:2, August 1952, pages 108-117.
Claims (1)
1. A PROCESS FOR THE PERMANENT DEFORMATION OF LIVE HUMAN HAIR, WHICH COMPRISES: (A) PREPARING A STOCK SOLUTION HAVING A PH OF BETWEEN 8 AND 9.5, FOR STORAGE PURPOSES, OF AN AQUEOUS SOLUTION OF AN AMIDE OF MERCAPTO ALKANOIC ACID OF THE GENERAL FORMULA
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR3063908X | 1958-05-29 |
Publications (1)
Publication Number | Publication Date |
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US3063908A true US3063908A (en) | 1962-11-13 |
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ID=9691500
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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US769097A Expired - Lifetime US3063908A (en) | 1958-05-29 | 1958-10-23 | Process for permanent deformation of hair |
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Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3213129A (en) * | 1960-12-15 | 1965-10-19 | Therachemie Chem Therapeut | Composition consisting of a mercapto compound and an organic phosphorus acid derivative as a color stabilizer |
US3395216A (en) * | 1964-11-09 | 1968-07-30 | Clairol Inc | Process for uniformly waving damaged hair |
US3674038A (en) * | 1968-02-20 | 1972-07-04 | Oreal | Treatment of human hair with zinc and cadmium dithiolate derivatives |
US4361157A (en) * | 1979-03-05 | 1982-11-30 | James Odie R | Method of curling negroid hair without rollers |
US5775342A (en) * | 1996-05-10 | 1998-07-07 | Dep Corporation | Hair waving method using acidic reducing solution containing alcohol amine sulfite |
Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2464280A (en) * | 1945-03-07 | 1949-03-15 | Raymond Lab Inc | Cream hair treating preparations |
US2631965A (en) * | 1950-05-24 | 1953-03-17 | Ernst O Schnell | Permanent waving of hair |
US2688972A (en) * | 1951-11-20 | 1954-09-14 | Gillette Co | Process for permanently waving human hair |
US2714119A (en) * | 1953-08-07 | 1955-07-26 | Sterling Drug Inc | Process for preparing amides of alphamercapto lower fatty acids |
US2717228A (en) * | 1951-04-23 | 1955-09-06 | Gillette Co | Hair waving composition |
US2889833A (en) * | 1951-12-03 | 1959-06-09 | Sales Affiliates Inc | Glyceryl monomercaptan composition and method of cold waving |
-
1958
- 1958-10-23 US US769097A patent/US3063908A/en not_active Expired - Lifetime
Patent Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2464280A (en) * | 1945-03-07 | 1949-03-15 | Raymond Lab Inc | Cream hair treating preparations |
US2631965A (en) * | 1950-05-24 | 1953-03-17 | Ernst O Schnell | Permanent waving of hair |
US2717228A (en) * | 1951-04-23 | 1955-09-06 | Gillette Co | Hair waving composition |
US2688972A (en) * | 1951-11-20 | 1954-09-14 | Gillette Co | Process for permanently waving human hair |
US2889833A (en) * | 1951-12-03 | 1959-06-09 | Sales Affiliates Inc | Glyceryl monomercaptan composition and method of cold waving |
US2714119A (en) * | 1953-08-07 | 1955-07-26 | Sterling Drug Inc | Process for preparing amides of alphamercapto lower fatty acids |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3213129A (en) * | 1960-12-15 | 1965-10-19 | Therachemie Chem Therapeut | Composition consisting of a mercapto compound and an organic phosphorus acid derivative as a color stabilizer |
US3395216A (en) * | 1964-11-09 | 1968-07-30 | Clairol Inc | Process for uniformly waving damaged hair |
US3674038A (en) * | 1968-02-20 | 1972-07-04 | Oreal | Treatment of human hair with zinc and cadmium dithiolate derivatives |
US4361157A (en) * | 1979-03-05 | 1982-11-30 | James Odie R | Method of curling negroid hair without rollers |
US5775342A (en) * | 1996-05-10 | 1998-07-07 | Dep Corporation | Hair waving method using acidic reducing solution containing alcohol amine sulfite |
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