GB908888A - Hair preparations - Google Patents
Hair preparationsInfo
- Publication number
- GB908888A GB908888A GB22986/60A GB2298660A GB908888A GB 908888 A GB908888 A GB 908888A GB 22986/60 A GB22986/60 A GB 22986/60A GB 2298660 A GB2298660 A GB 2298660A GB 908888 A GB908888 A GB 908888A
- Authority
- GB
- United Kingdom
- Prior art keywords
- acyl
- soluble
- alkylol
- alkyl
- acid
- 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
Links
- 239000003676 hair preparation Substances 0.000 title abstract 4
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 abstract 6
- 125000002252 acyl group Chemical group 0.000 abstract 6
- 239000003638 chemical reducing agent Substances 0.000 abstract 6
- 125000000217 alkyl group Chemical group 0.000 abstract 5
- -1 invert sugar Chemical compound 0.000 abstract 5
- 150000003839 salts Chemical class 0.000 abstract 5
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 abstract 4
- 125000004432 carbon atom Chemical group C* 0.000 abstract 4
- UMGDCJDMYOKAJW-UHFFFAOYSA-N thiourea Chemical compound NC(N)=S UMGDCJDMYOKAJW-UHFFFAOYSA-N 0.000 abstract 4
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 abstract 3
- 230000001476 alcoholic effect Effects 0.000 abstract 3
- 150000001298 alcohols Chemical class 0.000 abstract 3
- 235000014113 dietary fatty acids Nutrition 0.000 abstract 3
- 229930195729 fatty acid Natural products 0.000 abstract 3
- 239000000194 fatty acid Substances 0.000 abstract 3
- 239000002453 shampoo Substances 0.000 abstract 3
- 239000000344 soap Substances 0.000 abstract 3
- 150000003467 sulfuric acid derivatives Chemical class 0.000 abstract 3
- OWEGMIWEEQEYGQ-UHFFFAOYSA-N 100676-05-9 Natural products OC1C(O)C(O)C(CO)OC1OCC1C(O)C(O)C(O)C(OC2C(OC(O)C(O)C2O)CO)O1 OWEGMIWEEQEYGQ-UHFFFAOYSA-N 0.000 abstract 2
- GUBGYTABKSRVRQ-XLOQQCSPSA-N Alpha-Lactose Chemical compound O[C@@H]1[C@@H](O)[C@@H](O)[C@@H](CO)O[C@H]1O[C@@H]1[C@@H](CO)O[C@H](O)[C@H](O)[C@H]1O GUBGYTABKSRVRQ-XLOQQCSPSA-N 0.000 abstract 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract 2
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical class C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 abstract 2
- 229930091371 Fructose Natural products 0.000 abstract 2
- RFSUNEUAIZKAJO-ARQDHWQXSA-N Fructose Chemical compound OC[C@H]1O[C@](O)(CO)[C@@H](O)[C@@H]1O RFSUNEUAIZKAJO-ARQDHWQXSA-N 0.000 abstract 2
- 239000005715 Fructose Substances 0.000 abstract 2
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 abstract 2
- 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 abstract 2
- GUBGYTABKSRVRQ-QKKXKWKRSA-N Lactose Natural products OC[C@H]1O[C@@H](O[C@H]2[C@H](O)[C@@H](O)C(O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@H]1O GUBGYTABKSRVRQ-QKKXKWKRSA-N 0.000 abstract 2
- 239000004166 Lanolin Substances 0.000 abstract 2
- GUBGYTABKSRVRQ-PICCSMPSSA-N Maltose Natural products O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@@H]1O[C@@H]1[C@@H](CO)OC(O)[C@H](O)[C@H]1O GUBGYTABKSRVRQ-PICCSMPSSA-N 0.000 abstract 2
- 229920001800 Shellac Polymers 0.000 abstract 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 abstract 2
- XOCUXOWLYLLJLV-UHFFFAOYSA-N [O].[S] Chemical class [O].[S] XOCUXOWLYLLJLV-UHFFFAOYSA-N 0.000 abstract 2
- 239000002253 acid Substances 0.000 abstract 2
- 238000007792 addition Methods 0.000 abstract 2
- WQZGKKKJIJFFOK-PHYPRBDBSA-N alpha-D-galactose Chemical compound OC[C@H]1O[C@H](O)[C@H](O)[C@@H](O)[C@H]1O WQZGKKKJIJFFOK-PHYPRBDBSA-N 0.000 abstract 2
- 230000000844 anti-bacterial effect Effects 0.000 abstract 2
- 239000003899 bactericide agent Substances 0.000 abstract 2
- WQZGKKKJIJFFOK-VFUOTHLCSA-N beta-D-glucose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 abstract 2
- GUBGYTABKSRVRQ-QUYVBRFLSA-N beta-maltose Chemical compound OC[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O)[C@H](O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1O GUBGYTABKSRVRQ-QUYVBRFLSA-N 0.000 abstract 2
- OHJMTUPIZMNBFR-UHFFFAOYSA-N biuret Chemical compound NC(=O)NC(N)=O OHJMTUPIZMNBFR-UHFFFAOYSA-N 0.000 abstract 2
- 239000000872 buffer Substances 0.000 abstract 2
- 239000004202 carbamide Substances 0.000 abstract 2
- 239000004359 castor oil Substances 0.000 abstract 2
- 235000019438 castor oil Nutrition 0.000 abstract 2
- 150000001470 diamides Chemical class 0.000 abstract 2
- GRWZHXKQBITJKP-UHFFFAOYSA-N dithionous acid Chemical class OS(=O)S(O)=O GRWZHXKQBITJKP-UHFFFAOYSA-N 0.000 abstract 2
- 150000004665 fatty acids Chemical class 0.000 abstract 2
- 229930182830 galactose Natural products 0.000 abstract 2
- 239000008103 glucose Substances 0.000 abstract 2
- 239000005556 hormone Substances 0.000 abstract 2
- 229940088597 hormone Drugs 0.000 abstract 2
- 239000001257 hydrogen Substances 0.000 abstract 2
- 229910052739 hydrogen Inorganic materials 0.000 abstract 2
- 125000004435 hydrogen atom Chemical class [H]* 0.000 abstract 2
- 229960004903 invert sugar Drugs 0.000 abstract 2
- 239000008101 lactose Substances 0.000 abstract 2
- 235000019388 lanolin Nutrition 0.000 abstract 2
- 229940039717 lanolin Drugs 0.000 abstract 2
- 239000007788 liquid Substances 0.000 abstract 2
- 239000002480 mineral oil Substances 0.000 abstract 2
- 235000010446 mineral oil Nutrition 0.000 abstract 2
- 239000000203 mixture Substances 0.000 abstract 2
- 229910052760 oxygen Inorganic materials 0.000 abstract 2
- 239000000419 plant extract Substances 0.000 abstract 2
- 159000000001 potassium salts Chemical class 0.000 abstract 2
- 229920006395 saturated elastomer Polymers 0.000 abstract 2
- 239000004208 shellac Substances 0.000 abstract 2
- ZLGIYFNHBLSMPS-ATJNOEHPSA-N shellac Chemical compound OCCCCCC(O)C(O)CCCCCCCC(O)=O.C1C23[C@H](C(O)=O)CCC2[C@](C)(CO)[C@@H]1C(C(O)=O)=C[C@@H]3O ZLGIYFNHBLSMPS-ATJNOEHPSA-N 0.000 abstract 2
- 235000013874 shellac Nutrition 0.000 abstract 2
- 229940113147 shellac Drugs 0.000 abstract 2
- 229910052708 sodium Inorganic materials 0.000 abstract 2
- 239000011734 sodium Substances 0.000 abstract 2
- 239000007787 solid Substances 0.000 abstract 2
- 235000000346 sugar Nutrition 0.000 abstract 2
- 150000008163 sugars Chemical class 0.000 abstract 2
- 229910052717 sulfur Inorganic materials 0.000 abstract 2
- KRURGYOKPVLRHQ-UHFFFAOYSA-N trithionic acid Chemical compound OS(=O)(=O)SS(O)(=O)=O KRURGYOKPVLRHQ-UHFFFAOYSA-N 0.000 abstract 2
- 239000011782 vitamin Substances 0.000 abstract 2
- 229940088594 vitamin Drugs 0.000 abstract 2
- 229930003231 vitamin Natural products 0.000 abstract 2
- 235000013343 vitamin Nutrition 0.000 abstract 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 abstract 1
- 241000416162 Astragalus gummifer Species 0.000 abstract 1
- 229910019142 PO4 Inorganic materials 0.000 abstract 1
- 229920001615 Tragacanth Polymers 0.000 abstract 1
- 150000001242 acetic acid derivatives Chemical class 0.000 abstract 1
- 229910052783 alkali metal Inorganic materials 0.000 abstract 1
- 150000001340 alkali metals Chemical class 0.000 abstract 1
- 229920000180 alkyd Polymers 0.000 abstract 1
- JIRRNZWTWJGJCT-UHFFFAOYSA-N carbamothioylthiourea Chemical compound NC(=S)NC(N)=S JIRRNZWTWJGJCT-UHFFFAOYSA-N 0.000 abstract 1
- YCLDXRHGQVDVJR-UHFFFAOYSA-N carbamothioylurea Chemical compound NC(=O)NC(N)=S YCLDXRHGQVDVJR-UHFFFAOYSA-N 0.000 abstract 1
- 239000003599 detergent Substances 0.000 abstract 1
- 150000002170 ethers Chemical class 0.000 abstract 1
- 150000002190 fatty acyls Chemical group 0.000 abstract 1
- 150000002194 fatty esters Chemical class 0.000 abstract 1
- 235000011187 glycerol Nutrition 0.000 abstract 1
- 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 abstract 1
- 230000003370 grooming effect Effects 0.000 abstract 1
- 239000004615 ingredient Substances 0.000 abstract 1
- 239000004922 lacquer Substances 0.000 abstract 1
- 239000003921 oil Substances 0.000 abstract 1
- 235000021317 phosphate Nutrition 0.000 abstract 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 abstract 1
- 229920001521 polyalkylene glycol ether Polymers 0.000 abstract 1
- 229920000151 polyglycol Polymers 0.000 abstract 1
- 239000010695 polyglycol Substances 0.000 abstract 1
- 229920001451 polypropylene glycol Polymers 0.000 abstract 1
- 239000000843 powder Substances 0.000 abstract 1
- 150000005846 sugar alcohols Polymers 0.000 abstract 1
- 125000001273 sulfonato group Chemical group [O-]S(*)(=O)=O 0.000 abstract 1
- 239000000271 synthetic detergent Substances 0.000 abstract 1
- 230000001256 tonic effect Effects 0.000 abstract 1
- 239000012855 volatile organic compound Substances 0.000 abstract 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
- A61K8/30—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
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/40—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
- A61K8/42—Amides
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q5/00—Preparations for care of the hair
-
- 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
- A61Q5/02—Preparations for cleaning the hair
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Birds (AREA)
- Epidemiology (AREA)
- Cosmetics (AREA)
Abstract
A hair shampoo comprises 0,05 to 20% of a water-soluble skin-compatible reducing agent and 0,05 to 10% of a diamide having the formula:- <FORM:0908888/III/1> or <FORM:0908888/III/2> wherein X1 and X2 may be the same or different and represent O or S, and R1, R2, R3, R4 and R5 may be the same or different and represent hydrogen, alkyl, alkylol or acyl groups. The ratio of reducing agent to diamide is from 1:5 to 5:1. Specified reducing agents are water-soluble salts of sulphur oxygen acids having two or three sulphur atoms, e.g. salts of dithionous acid, thiosulphuric acid and trithionic acid particularly the sodium and potassium salts, and reducing sugars such as glucose, fructose, invert sugar, maltose, lactose and galactose. The diamides include urea, thiourea, buiret, thiobuiret, dithiobuiret and their water-soluble or alcohol soluble mono- and poly-alkyl alkylol and acyl derivatives. The alkyl, alkylol and acyl groups may be saturated or unsaturated, straight or branched chain and should not contain more than four carbon atoms. In the case of buiret derivatives it is preferred that the chain length of the groups should not exceed two carbon atoms. The shampoo may be liquid, e.g. an aqueous or alcoholic solution, paste or solid and contains conventional soaps or synthetic detergents, for example, alkyd sulphates and phosphates, fatty acyl mono-glyceride sulphates, fatty esters of hydroxyalkane sulphonates, alkanolamide sulphates, N-fatty acyl taurides, alkylaryl sulphonates, sulphated ethylene oxide condensates with fatty acids and alcohols and with alkylaryl radicals, and sulphonated oils, all of which may be present as the alkali metal, ammonium, or lower alkanolamine salts; ethylene oxide condensates with fatty acids and alcohols, alkylaryl radicals, polypropylene glycols or alkanolamides, or fatty acyl lysalbinates; N-acyl pyridinium halides or tetraalkylammonium halides, or the acetates or sulphates thereof; N-alkyl-b -aminopropionic acid. The detergent preferably comprises 5-40% of a liquid or paste composition and 15 to 98% of a solid or powder composition. The shampoo may also include castor or mineral oil, polyhydric alcohol, polyalkylene glycol ethers, fatty acid esters of alcohols or polyglycol ethers, gum tragacanth and shellac. The pH is preferably 4 to 10 but in soap containing hair preparations it is above 8. Optional additions are vitamins, hormones, lanolin, bactericides, plant extracts and buffers. Specification 907,188 is referred to.ALSO:A hair preparation comprises 0.05 to 20% of a water-soluble skin-compatible reducing agent and 0.05 to 10% of a diamide having the formula <FORM:0908888/VI/1> wherein X1 and X2 may be the same or different and represent O or S, and R1, R2, R3, R4 and R5 may be the same or different and represent hydrogen, alkyl, alkylol or acyl groups. The ratio of reducing agent to diamide is from 1 : 5 to 5 : 1. Specified reducing agents are water-soluble salts of sulphur oxygen acids having two or three sulphur atoms, e.g. salts of dithionous acid, thiosulphuric acid and trithionic acid particularly the sodium and potassium salts, and reducing sugars such as glucose, fructose, invert sugar, maltose, lactose and galactose. The diamides include urea, thiourea, biuret, thiobiuret, dithiobiuret and their water-soluble or alcohol soluble mono- and polyalkyl alkylol and acyl derivatives. The alkyl, alkylol and acyl groups may be saturated or unsaturated, straight or branched chain and should not contain more than four carbon atoms. In the case of biuret derivatives it is preferred that the chain length of the groups should not exceed two carbon atoms. The hair tonic or dressing may take the form of an aqueous, alcoholic or aqueous alcoholic solution. An optional ingredient is a non-volatile organic compound which facilitates hair grooming, e.g. castor oil, mineral oil, glycerol, gums and lacquers such as shellac. The pH is preferably 4 to 10 but in soap containing hair preparations it is above 8. Optional additions are vitamins, hormones, lanolin, bactericides, plant extracts and buffers. Specification 907,188 is referred to.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DEP23120A DE1134477B (en) | 1959-07-09 | 1959-07-09 | Hair care products |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB908888A true GB908888A (en) | 1962-10-24 |
Family
ID=7369057
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB22986/60A Expired GB908888A (en) | 1959-07-09 | 1960-06-30 | Hair preparations |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US3149042A (en) |
| BE (1) | BE592793A (en) |
| CH (1) | CH443567A (en) |
| DE (1) | DE1134477B (en) |
| GB (1) | GB908888A (en) |
| NL (2) | NL140725B (en) |
| SE (1) | SE301023B (en) |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2159400A1 (en) * | 1971-11-11 | 1973-06-22 | Indal Oy | |
| US4043829A (en) | 1971-08-26 | 1977-08-23 | Sun Oil Company Of Pennsylvania | Stabilized wax emulsions |
| GB2136445A (en) * | 1983-03-16 | 1984-09-19 | Colgate Palmolive Co | Non-antimicrobial deodorant cleansing composition |
| DE3514087A1 (en) * | 1985-04-18 | 1986-10-23 | Laszlo Dr Med Szekely | Hair treatment composition and process for the cosmetic treatment of hair and hair matrix |
| WO2004024106A2 (en) * | 2002-09-05 | 2004-03-25 | Chanh-Dinh Nguyen-Petersen | Use of a cosmetic care product containing urea and cosmetic care product containing urea |
Families Citing this family (23)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CH427149A (en) * | 1963-01-24 | 1966-12-31 | Joos Bernhard | Nail and hair treatment preparations |
| FR1569578A (en) * | 1967-07-27 | 1969-06-06 | ||
| US3757804A (en) * | 1968-07-18 | 1973-09-11 | Fr Sa | Product for treating hair |
| GB1314616A (en) * | 1970-08-27 | 1973-04-26 | Beecham Group Ltd | Shampoos |
| US3773056A (en) * | 1971-03-05 | 1973-11-20 | Oreal | Compositions and methods of improving the quality of human hair with stable methylol compounds |
| US3960782A (en) * | 1974-09-27 | 1976-06-01 | The Procter & Gamble Company | Shampoo compositions which impart high luster and manageability to hair |
| GB1501019A (en) * | 1975-04-03 | 1978-02-15 | Borchorst B | Shampoo |
| US4137302A (en) * | 1976-04-02 | 1979-01-30 | Lever Brothers Company | Cosmetic composition |
| JPS54140553A (en) * | 1978-04-24 | 1979-10-31 | Senju Pharma Co | Contact lens washing liquid |
| DE2824025B2 (en) * | 1978-06-01 | 1981-04-16 | Henkel KGaA, 4000 Düsseldorf | Use of glucose to improve the structure and the wet combability of hair |
| US4272413A (en) * | 1979-11-26 | 1981-06-09 | Colgate-Palmolive Company | Dialkylurea textile softening and antistatic agents |
| US4268406A (en) * | 1980-02-19 | 1981-05-19 | The Procter & Gamble Company | Liquid detergent composition |
| US4364837A (en) * | 1981-09-08 | 1982-12-21 | Lever Brothers Company | Shampoo compositions comprising saccharides |
| NZ203201A (en) * | 1982-02-12 | 1985-01-31 | Smith & Nephew Ass | Sulphur dioxide-releasing composition containing hydroquinone |
| AU1672383A (en) * | 1982-07-30 | 1984-02-02 | Helene Curtis Industries Inc. | Aqueous urea containing hair waving composition |
| US4822604A (en) * | 1985-05-20 | 1989-04-18 | S. C. Johnson & Son, Inc. | Local treatment of dandruff, seborrheic dermatitis, and psoriasis |
| US5019376A (en) * | 1989-03-13 | 1991-05-28 | S. C. Johnson & Son, Inc. | Sparkling pearlescent personal care compositions |
| FR2750334B1 (en) * | 1996-07-01 | 1998-09-04 | Oreal | USE OF AMINO-ALCOHOLS DERIVATIVES WITH UREA FUNCTION IN AND FOR THE PREPARATION OF COSMETIC OR DERMATOLOGICAL COMPOSITIONS |
| EP1300136A3 (en) * | 2001-10-04 | 2003-05-14 | Henkel Kommanditgesellschaft auf Aktien | Method for modification of hair coloration based on dithionite salts |
| JP2003327516A (en) * | 2002-05-10 | 2003-11-19 | Kao Corp | Curly hair straightening agent composition |
| JP4869577B2 (en) * | 2004-09-30 | 2012-02-08 | アクゾノーベル株式会社 | Hair cosmetics |
| WO2006056692A1 (en) * | 2004-11-26 | 2006-06-01 | L'oreal | Cosmetic composition comprising at least one fixing polymer and at least one hydroxyalkyl urea |
| FR2878436B1 (en) * | 2004-11-26 | 2007-03-30 | Oreal | COSMETIC COMPOSITION COMPRISING AT LEAST ONE FIXING POLYMER AND AT LEAST ONE HYDROXYALKYL UREA |
Family Cites Families (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE5922C (en) * | G. M. WEIDENHAMMER in Aglasterhausen | Devices for making whip handles and similar objects | ||
| US2293551A (en) * | 1938-07-14 | 1942-08-18 | Eric C Kunz | Esters of aliphatic acids with isopropyl alcohol |
| US2342150A (en) * | 1940-10-24 | 1944-02-22 | Johnson Marsh Corp | Wetting composition |
| US2551627A (en) * | 1941-01-02 | 1951-05-08 | Norsk Sulfo Aktieselskap | Stabilized polythionates as medicinal cosmetics |
| BE452783A (en) * | 1941-01-02 | |||
| DE930581C (en) * | 1949-12-09 | 1955-07-21 | Hanns Dr Schuberth | Hair care products |
| US2600624A (en) * | 1950-03-15 | 1952-06-17 | Alice Parker | Hair-waving composition |
| BE504346A (en) * | 1950-06-30 | |||
| GB698767A (en) * | 1950-07-06 | 1953-10-21 | Bayer Ag | Readily soluble dry preparations of swelling substances |
| US2773835A (en) * | 1951-11-16 | 1956-12-11 | Colgate Palmolive Co | Liquid shampoo composition |
| US2771394A (en) * | 1953-07-10 | 1956-11-20 | Colgate Palmolive Co | Hair grooming preparation |
| DE950678C (en) * | 1953-12-06 | 1956-10-11 | Basf Ag | Hair care products |
-
0
- BE BE592793D patent/BE592793A/xx unknown
- NL NL253568D patent/NL253568A/xx unknown
-
1959
- 1959-07-09 DE DEP23120A patent/DE1134477B/en active Pending
-
1960
- 1960-06-16 CH CH685260A patent/CH443567A/en unknown
- 1960-06-24 US US38459A patent/US3149042A/en not_active Expired - Lifetime
- 1960-06-30 GB GB22986/60A patent/GB908888A/en not_active Expired
- 1960-07-06 SE SE6621/60A patent/SE301023B/xx unknown
- 1960-07-08 NL NL60253568A patent/NL140725B/en not_active IP Right Cessation
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4043829A (en) | 1971-08-26 | 1977-08-23 | Sun Oil Company Of Pennsylvania | Stabilized wax emulsions |
| FR2159400A1 (en) * | 1971-11-11 | 1973-06-22 | Indal Oy | |
| GB2136445A (en) * | 1983-03-16 | 1984-09-19 | Colgate Palmolive Co | Non-antimicrobial deodorant cleansing composition |
| FR2542755A1 (en) * | 1983-03-16 | 1984-09-21 | Colgate Palmolive Co | NON-ANTIMICROBIAL DEODORANT CLEANING COMPOSITION AND METHOD USING THE SAME |
| DE3514087A1 (en) * | 1985-04-18 | 1986-10-23 | Laszlo Dr Med Szekely | Hair treatment composition and process for the cosmetic treatment of hair and hair matrix |
| WO2004024106A2 (en) * | 2002-09-05 | 2004-03-25 | Chanh-Dinh Nguyen-Petersen | Use of a cosmetic care product containing urea and cosmetic care product containing urea |
| WO2004024106A3 (en) * | 2002-09-05 | 2004-05-21 | Chanh-Dinh Nguyen-Petersen | Use of a cosmetic care product containing urea and cosmetic care product containing urea |
Also Published As
| Publication number | Publication date |
|---|---|
| BE592793A (en) | |
| US3149042A (en) | 1964-09-15 |
| NL253568A (en) | |
| CH443567A (en) | 1967-09-15 |
| NL140725B (en) | 1974-01-15 |
| SE301023B (en) | 1968-05-20 |
| DE1134477B (en) | 1962-08-09 |
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