US2100090A - Cosmetic products - Google Patents
Cosmetic products Download PDFInfo
- Publication number
- US2100090A US2100090A US41024A US4102435A US2100090A US 2100090 A US2100090 A US 2100090A US 41024 A US41024 A US 41024A US 4102435 A US4102435 A US 4102435A US 2100090 A US2100090 A US 2100090A
- Authority
- US
- United States
- Prior art keywords
- decomposition products
- molecular weight
- high molecular
- fatty acid
- higher fatty
- 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
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- 239000002537 cosmetic Substances 0.000 title description 13
- 239000000047 product Substances 0.000 description 49
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 44
- 238000000354 decomposition reaction Methods 0.000 description 36
- 150000004665 fatty acids Chemical group 0.000 description 28
- 239000002253 acid Substances 0.000 description 26
- 229910052757 nitrogen Inorganic materials 0.000 description 22
- 239000000344 soap Substances 0.000 description 21
- 238000007792 addition Methods 0.000 description 11
- 150000001447 alkali salts Chemical class 0.000 description 10
- 239000003795 chemical substances by application Substances 0.000 description 9
- 238000005406 washing Methods 0.000 description 9
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 6
- 239000007788 liquid Substances 0.000 description 6
- 239000002674 ointment Substances 0.000 description 5
- 239000000243 solution Substances 0.000 description 5
- 239000000606 toothpaste Substances 0.000 description 5
- 239000006071 cream Substances 0.000 description 4
- 235000014113 dietary fatty acids Nutrition 0.000 description 4
- 229930195729 fatty acid Natural products 0.000 description 4
- 239000000194 fatty acid Substances 0.000 description 4
- 238000002360 preparation method Methods 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- 239000003513 alkali Substances 0.000 description 3
- 239000007859 condensation product Substances 0.000 description 3
- 239000003814 drug Substances 0.000 description 3
- 239000000839 emulsion Substances 0.000 description 3
- 239000003921 oil Substances 0.000 description 3
- 235000019198 oils Nutrition 0.000 description 3
- 229940034610 toothpaste Drugs 0.000 description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- 235000010469 Glycine max Nutrition 0.000 description 2
- 244000068988 Glycine max Species 0.000 description 2
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 2
- 230000001804 emulsifying effect Effects 0.000 description 2
- IPCSVZSSVZVIGE-UHFFFAOYSA-N hexadecanoic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 239000008257 shaving cream Substances 0.000 description 2
- OYHQOLUKZRVURQ-NTGFUMLPSA-N (9Z,12Z)-9,10,12,13-tetratritiooctadeca-9,12-dienoic acid Chemical compound C(CCCCCCC\C(=C(/C\C(=C(/CCCCC)\[3H])\[3H])\[3H])\[3H])(=O)O OYHQOLUKZRVURQ-NTGFUMLPSA-N 0.000 description 1
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 1
- MLQBTMWHIOYKKC-KTKRTIGZSA-N (z)-octadec-9-enoyl chloride Chemical compound CCCCCCCC\C=C/CCCCCCCC(Cl)=O MLQBTMWHIOYKKC-KTKRTIGZSA-N 0.000 description 1
- NGNBDVOYPDDBFK-UHFFFAOYSA-N 2-[2,4-di(pentan-2-yl)phenoxy]acetyl chloride Chemical compound CCCC(C)C1=CC=C(OCC(Cl)=O)C(C(C)CCC)=C1 NGNBDVOYPDDBFK-UHFFFAOYSA-N 0.000 description 1
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 1
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 1
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- 239000005639 Lauric acid Substances 0.000 description 1
- 239000005642 Oleic acid Substances 0.000 description 1
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 1
- 235000021314 Palmitic acid Nutrition 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- 239000005864 Sulphur Substances 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
- 235000011941 Tilia x europaea Nutrition 0.000 description 1
- 239000012670 alkaline solution Substances 0.000 description 1
- DTOSIQBPPRVQHS-PDBXOOCHSA-N alpha-linolenic acid Chemical compound CC\C=C/C\C=C/C\C=C/CCCCCCCC(O)=O DTOSIQBPPRVQHS-PDBXOOCHSA-N 0.000 description 1
- 235000020661 alpha-linolenic acid Nutrition 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 150000003863 ammonium salts Chemical class 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 239000004359 castor oil Substances 0.000 description 1
- 235000019438 castor oil Nutrition 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- BNIILDVGGAEEIG-UHFFFAOYSA-L disodium hydrogen phosphate Chemical compound [Na+].[Na+].OP([O-])([O-])=O BNIILDVGGAEEIG-UHFFFAOYSA-L 0.000 description 1
- 229910000397 disodium phosphate Inorganic materials 0.000 description 1
- 235000019800 disodium phosphate Nutrition 0.000 description 1
- 238000004945 emulsification Methods 0.000 description 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 description 1
- 150000004820 halides Chemical class 0.000 description 1
- 239000008233 hard water Substances 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- 239000011630 iodine Substances 0.000 description 1
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
- 239000004571 lime Substances 0.000 description 1
- 229960004488 linolenic acid Drugs 0.000 description 1
- KQQKGWQCNNTQJW-UHFFFAOYSA-N linolenic acid Natural products CC=CCCC=CCC=CCCCCCCCC(O)=O KQQKGWQCNNTQJW-UHFFFAOYSA-N 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000001525 mentha piperita l. herb oil Substances 0.000 description 1
- WQEPLUUGTLDZJY-UHFFFAOYSA-N n-Pentadecanoic acid Natural products CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-UHFFFAOYSA-N 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- 235000021313 oleic acid Nutrition 0.000 description 1
- 125000001117 oleyl 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])=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])[H] 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 235000019477 peppermint oil Nutrition 0.000 description 1
- WBHHMMIMDMUBKC-XLNAKTSKSA-N ricinelaidic acid Chemical compound CCCCCC[C@@H](O)C\C=C\CCCCCCCC(O)=O WBHHMMIMDMUBKC-XLNAKTSKSA-N 0.000 description 1
- 229960003656 ricinoleic acid Drugs 0.000 description 1
- FEUQNCSVHBHROZ-UHFFFAOYSA-N ricinoleic acid Natural products CCCCCCC(O[Si](C)(C)C)CC=CCCCCCCCC(=O)OC FEUQNCSVHBHROZ-UHFFFAOYSA-N 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 150000004671 saturated fatty acids Chemical class 0.000 description 1
- 239000001488 sodium phosphate Substances 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 235000012424 soybean oil Nutrition 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 125000004079 stearyl 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])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 239000003784 tall oil Substances 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
- 150000004670 unsaturated fatty acids Chemical group 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
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/64—Proteins; Peptides; Derivatives or degradation products thereof
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q11/00—Preparations for care of the teeth, of the oral cavity or of dentures; Dentifrices, e.g. toothpastes; Mouth rinses
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q9/00—Preparations for removing hair or for aiding hair removal
- A61Q9/02—Shaving preparations
-
- 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
- Y10S516/00—Colloid systems and wetting agents; subcombinations thereof; processes of
- Y10S516/01—Wetting, emulsifying, dispersing, or stabilizing agents
- Y10S516/06—Protein or carboxylic compound containing
Definitions
- the invention relates to cosmetic products, such as toilet soap, liquid soaps, hair-washing agents, shaving soaps, shaving creams, salves, creams, toothpastes, and similar products.
- cosmetic products according to the invention contain'albumen decomposition products of high molecular weight acylated at the nitrogen with higher fatty acid residues.
- suitable substituents of the albumen decomposition products of high molecular weight are the residues of the following acids: lauric acid, palmitic acid, stearic acid, oleic acid, ricinoleic acid, soyabean acid, linoleic acid, linolenic acid, the acids of talloil.
- albumen decomposition products of high molecular weight there come into consideration chiefly those of the type of lysalbinic acid and protalbinic acid.
- the new cosmetic products have numerous advantageous properties on account of the content of albumen decomposition products of high molecular weight substituted at thenitrogen by higher fatty acid residues.
- the soaps according to the invention can be used also without difficulty in hard water, because the albumen decomposition products of high molecular Weight acylated at the nitrogen with higher fatty acid residues are not only themselves lime-stable, but also permit a better emulsification of lime soap.
- the emulsifying property of albumen decomposition products of high molecular weight substituted at the nitrogen by higher fatty acid residues is especially very strongly marked. Precisely on account of this property, these compounds are suitable as additions to salves, creams, and toothpastes, if desired with other salve bases which are known per se.
- the new products are suitable as additions to soaps of all kinds, for example also as an addition to shaving soap. Since the albumen decomposition products of high molecular weight acylated at the nitrogen with higher fatty acid residues are somewhat hygroscopic, the lather of soaps that contain this addition is less inclined to dry up than the lather of In Germany September 20,
- acylated albumen decomposition products have also proved Very satisfactory as an addition to liquid soaps.
- the liquid soaps are sometimes somewhat thickened; if it is desired to counteract this, sulphonated oils may also be added to the liquid soap.
- the said albumen decomposition products are also suitable as hair Washing agents or as additions to hair washing agents. If it is desired to avoid the presence of soap there may be obtained a Well-lathering and soapand alkali-free hair washing agent.
- the acylated products can be used directly. If on the contrary it is desired to have a clear solution, there are advantageously used the water-soluble alkali or ammonium salts of the acylated products.
- the production of the albumen decomposition products of high molecular weight substituted at the nitrogen by higher fatty acid residues is effected in a known wayby causing the halides of higher fatty acids to react in alkaline solution with albumen decomposition products.
- a viscous oil which is'an approximately per cent solution of the alkali salts of the albumen decomposition products of high molecular weight substituted at the nitrogen by higher fatty acid residues.
- Quite neutral-reacting products can be obtained by correct measuring of the amount of alkali or by supplementary addition of acid or bufier salts.
- Example 2 To 100 parts of an ordinary liquid hair soap there are added 8 parts of a 30 per cent solution of the condensation product of soya fatty acid chloride and lysalbinic acid and two parts of a sulphonated castor oil.
- the liquid soap provided with this addition is quite lime-stable.
- Example 3 l grammes of colloidal sulphur are mixed with 40 grammes of e 40 per cent emulsion of stearyl lysalbinic acid in water. There is obtained in this Way a very stable and efiicacious sulphur salve.
- Example 4 30 grammes of acetic acid alumina solution DAB VI are mixed with '70 grammes of a 50 per cent emulsion of oleyl lysalbinic acid in water.
- the acetic acid alumina salve thus obtained is practically indefinitely stable.
- Example 5 1000 grammes of a per cent solution of the sodium salt of the condensation product of soyaoil acid chloride and albumen decomposition products of the type of lysalbinic acid and protalbinic acid are mixed with 100 grammes of 30 per cent hydrogen peroxide, grammes of tartaric acid, 1!) grammes of crystalline disodium phosphate, grammes of water, 5 grammes of sweetening material, 50 grammes of peppermint oil, and 100 grammes of alcohol. There is obtained in this way a tooth paste that is gelatinous, stable. and very efllcacious in consequence of its oxygen content.
- Example 6 280 grammes of the condensation product of oleic acid chloride and albumen decomposition products, which is neutralized with ammonia and standardized to 40 per cent dry content, 140
- a cosmetic Washing agent consisting of alkali salts of albumen decomposition products of high molecular weight substituted at the nitrogen by higher fatty acid residues.
- a preparation for application to the skin containing medicaments and albumen decomposition products of high molecular weight substituted at the nitrogen by higher fatty acid residues.
- a preparation for application to the skin containing medicaments and alkali salts of albumen decomposition products of high molecular weight substituted at the nitrogen by higher fatty acid residues.
- a preparation for application to the skin containing medicaments and albumen decomposition products of high molecular Weight substituted at the nitrogen by higher fatty acid residues, said albumen decomposition products being selected from the group consisting of lysalbinic acid and protalbinie acid.
- a tooth paste containing albumen decomposition products of high molecular weight substituted at the nitrogen by higher fatty acid residues.
- a tooth paste containing albumen decomposition products of high molecular weight substituted at the nitrogen by higher fatty acid residues said albumen decomposition products being selected from the group consisting of lysalbinie acid and protalbinic acid.
Description
ratented NOV. Z5, 1957 UNITED STATES wearers noom PATENT OFFICE.
COSMETIC PRODUCTS No Drawing. Application September 18, 1935, Se-
rial No. 41,024. 1934 Claims.
The invention relates to cosmetic products, such as toilet soap, liquid soaps, hair-washing agents, shaving soaps, shaving creams, salves, creams, toothpastes, and similar products.
cosmetic products according to the invention contain'albumen decomposition products of high molecular weight acylated at the nitrogen with higher fatty acid residues.
As higher fatty acid residues there come into consideration those that contain eight or more carbon atoms, preferably however the saturated or unsaturated fatty acid residues with 12-18 carbon atoms such as are contained in the natural fatty acids. Accordingly for example suitable substituents of the albumen decomposition products of high molecular weight are the residues of the following acids: lauric acid, palmitic acid, stearic acid, oleic acid, ricinoleic acid, soyabean acid, linoleic acid, linolenic acid, the acids of talloil.
As albumen decomposition products of high molecular weight there come into consideration chiefly those of the type of lysalbinic acid and protalbinic acid.
The new cosmetic products have numerous advantageous properties on account of the content of albumen decomposition products of high molecular weight substituted at thenitrogen by higher fatty acid residues. Thus for example the soaps according to the invention can be used also without difficulty in hard water, because the albumen decomposition products of high molecular Weight acylated at the nitrogen with higher fatty acid residues are not only themselves lime-stable, but also permit a better emulsification of lime soap. The emulsifying property of albumen decomposition products of high molecular weight substituted at the nitrogen by higher fatty acid residues is especially very strongly marked. Precisely on account of this property, these compounds are suitable as additions to salves, creams, and toothpastes, if desired with other salve bases which are known per se.
t is further of importance that the lathering power of the soap is not reduced by the albumen decomposition products of high molecular weight acylated at the nitrogen with higher fatty acid residues. Therefore the new products are suitable as additions to soaps of all kinds, for example also as an addition to shaving soap. Since the albumen decomposition products of high molecular weight acylated at the nitrogen with higher fatty acid residues are somewhat hygroscopic, the lather of soaps that contain this addition is less inclined to dry up than the lather of In Germany September 20,
\ ordinary shaving soap. When the shaving soap containing the addition according to the invention is made with a sufficiently large addition of water, there is obtained a stable and non-decomposing shaving cream in consequence of the great emulsifying capacity of the albumen decomposition products of high molecular weight acylated at the nitrogen with higher fatty acid residues.
The said acylated albumen decomposition products have also proved Very satisfactory as an addition to liquid soaps. By means of this addition the liquid soaps are sometimes somewhat thickened; if it is desired to counteract this, sulphonated oils may also be added to the liquid soap.
The said albumen decomposition products are also suitable as hair Washing agents or as additions to hair washing agents. If it is desired to avoid the presence of soap there may be obtained a Well-lathering and soapand alkali-free hair washing agent. For the making of emulsions, such as are used for example for selves and creams, the acylated products can be used directly. If on the contrary it is desired to have a clear solution, there are advantageously used the water-soluble alkali or ammonium salts of the acylated products.
The production of the albumen decomposition products of high molecular weight substituted at the nitrogen by higher fatty acid residues is effected in a known wayby causing the halides of higher fatty acids to react in alkaline solution with albumen decomposition products. By carrying out this reaction in a suitable concentration there is obtained a viscous oil which is'an approximately per cent solution of the alkali salts of the albumen decomposition products of high molecular weight substituted at the nitrogen by higher fatty acid residues. Quite neutral-reacting products can be obtained by correct measuring of the amount of alkali or by supplementary addition of acid or bufier salts.
The following examples may serve to illustrate the invention:-
Examplel 30 grammes of fatty acid with an'average acid number of 222 and an average iodine number of lathering shaving cream the lather of which has no tendency to dry up.
Example 2 To 100 parts of an ordinary liquid hair soap there are added 8 parts of a 30 per cent solution of the condensation product of soya fatty acid chloride and lysalbinic acid and two parts of a sulphonated castor oil. The liquid soap provided with this addition is quite lime-stable.
Example 3 l grammes of colloidal sulphur are mixed with 40 grammes of e 40 per cent emulsion of stearyl lysalbinic acid in water. There is obtained in this Way a very stable and efiicacious sulphur salve.
Example 4 30 grammes of acetic acid alumina solution DAB VI are mixed with '70 grammes of a 50 per cent emulsion of oleyl lysalbinic acid in water. The acetic acid alumina salve thus obtained is practically indefinitely stable.
Example 5 1000 grammes of a per cent solution of the sodium salt of the condensation product of soyaoil acid chloride and albumen decomposition products of the type of lysalbinic acid and protalbinic acid are mixed with 100 grammes of 30 per cent hydrogen peroxide, grammes of tartaric acid, 1!) grammes of crystalline disodium phosphate, grammes of water, 5 grammes of sweetening material, 50 grammes of peppermint oil, and 100 grammes of alcohol. There is obtained in this way a tooth paste that is gelatinous, stable. and very efllcacious in consequence of its oxygen content.
Example 6 280 grammes of the condensation product of oleic acid chloride and albumen decomposition products, which is neutralized with ammonia and standardized to 40 per cent dry content, 140
grammes of prepared chalk, 125 grammes of residues.
2. A cosmetic product containing the alkali salts of albumen decomposition products of high molecular weight substituted at the nitrogen by higher fatty acid residues.
3, A cosmetic product containing albumen decomposition products of high molecular weight substituted at the nitrogen by higher fatty acid residues, said albumen decomposition products being selected from the group consisting of lysalbinic acid and protalbinic acid.
4. A cosmetic product containing the alkali salts of albumen decomposition products of high molecular weight substituted at the nitrogen by higher fatty acid residues, said albumen decomposition products being selected from the group consisting of lysalbinic acid and protalbinic acid.
5. A cosmetic Washing agent consisting of alkali salts of albumen decomposition products of high molecular weight substituted at the nitrogen by higher fatty acid residues.
6. A cosmetic washing agent containing soap and alkali salts of albumen decomposition products of high molecular weight substituted at the nitrogen by higher fatty acid residues.
7. A cosmetic washing agent containing soap, alkali salts of albumen decomposition products of high molecular weight substituted at the nitrogen by higher fatty acid residues, and sulphonatedoils.
8. A cosmetic washing agent containing soap and alkalisalts of albumen decomposition products of high molecular weight substituted at the nitrogen by higher fatty acid residues, said albu men decomposition products being selected from the group consisting of lysalbinic acid and protalbinic acid.
9. A cosmetic washing agent containing soap, alkali salts of albumen decomposition products of high molecular weight substituted at the nitrogen by higher fatty acid residues, said albumen decomposition products being selected from the group consisting of lysalbinic acid and protalbinic acid, and sulphonated oils.
10. A preparation for application to the skin containing medicaments and albumen decomposition products of high molecular weight substituted at the nitrogen by higher fatty acid residues.
11. A preparation for application to the skin containing medicaments and alkali salts of albumen decomposition products of high molecular weight substituted at the nitrogen by higher fatty acid residues.
12. A preparation for application to the skin containing medicaments and albumen decomposition products of high molecular Weight substituted at the nitrogen by higher fatty acid residues, said albumen decomposition products being selected from the group consisting of lysalbinic acid and protalbinie acid.
13. A preparation for application to the skin containingmedicaments and alkali. salts of albumen decompcsition products of high molecular weight substituted at the nitrogen by higher fatty acid residues, said albumen decomposition products being selected from the group consisting of lysalbinic acid and protalbinic acid.
14. A tooth paste containing albumen decomposition products of high molecular weight substituted at the nitrogen by higher fatty acid residues.
15. A tooth paste containing albumen decomposition products of high molecular weight substituted at the nitrogen by higher fatty acid residues, said albumen decomposition products being selected from the group consisting of lysalbinie acid and protalbinic acid.
FRITZ SOMMER. MAX NASSAU.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE462977X | 1934-09-20 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2100090A true US2100090A (en) | 1937-11-23 |
Family
ID=6540048
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US41024A Expired - Lifetime US2100090A (en) | 1934-09-20 | 1935-09-18 | Cosmetic products |
Country Status (3)
| Country | Link |
|---|---|
| US (1) | US2100090A (en) |
| FR (1) | FR795052A (en) |
| GB (1) | GB462977A (en) |
Cited By (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE860095C (en) * | 1948-10-02 | 1952-12-18 | Mack Chem Pharm | Skin-friendly, foaming shaving agents |
| US2763269A (en) * | 1952-02-01 | 1956-09-18 | Rayette Inc | Foaming hair coloring compositions comprising basic dyes, and method of use |
| US3004897A (en) * | 1955-02-09 | 1961-10-17 | Shore Joseph | Dental preparation |
| US3954725A (en) * | 1972-03-13 | 1976-05-04 | Wilson Pharmaceutical & Chemical Corporation | Alcohol soluble acylated protein hydrolyzate reaction products |
| US4128543A (en) * | 1977-01-24 | 1978-12-05 | Inolex Corporation | Process for preparing alcohol soluble condensates of abietic acid and a protein hydrolysate |
| US4229429A (en) * | 1978-09-20 | 1980-10-21 | Inolex Corporation | Process for preparing alcohol soluble condensates of abietic acid and a protein hydrolsate |
| US4661340A (en) * | 1983-06-06 | 1987-04-28 | Interkemia Vegyipari Gazdasagi Tarsasag | Quail egg based stabilized foam compositions for cosmetic purposes |
| US5071960A (en) * | 1989-09-07 | 1991-12-10 | Hoechst Aktiengesellschaft | High molecular weight protein/fatty acid condensation products which are very well tolerated by the skin and mucosa |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NL104948C (en) * | 1952-02-15 | |||
| US2772203A (en) * | 1952-04-03 | 1956-11-27 | Colgate Palmolive Co | Stable dental creams containing higher aliphatic acyl amide of aminocarboxxylic acid compound |
| US2772204A (en) * | 1954-09-13 | 1956-11-27 | Colgate Palmolive Co | Dental preparations containing higher aliphatic acyl sarcoside compounds |
| US4485091A (en) * | 1980-07-15 | 1984-11-27 | Quinoderm Limited | Dermatological compositions |
| IT1297111B1 (en) * | 1997-12-10 | 1999-08-03 | Keminova Italiana S R L | PROCEDURE TO OBTAIN LIPOPROTEINS, LIPOAMINO ACIDS, LIPID ESTERS AND GLUCOLIPIDS, STARTING FROM OLIVE OIL AND / OR ITS |
-
1935
- 1935-09-12 GB GB25379/35A patent/GB462977A/en not_active Expired
- 1935-09-16 FR FR795052D patent/FR795052A/en not_active Expired
- 1935-09-18 US US41024A patent/US2100090A/en not_active Expired - Lifetime
Cited By (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE860095C (en) * | 1948-10-02 | 1952-12-18 | Mack Chem Pharm | Skin-friendly, foaming shaving agents |
| US2763269A (en) * | 1952-02-01 | 1956-09-18 | Rayette Inc | Foaming hair coloring compositions comprising basic dyes, and method of use |
| US3004897A (en) * | 1955-02-09 | 1961-10-17 | Shore Joseph | Dental preparation |
| US3954725A (en) * | 1972-03-13 | 1976-05-04 | Wilson Pharmaceutical & Chemical Corporation | Alcohol soluble acylated protein hydrolyzate reaction products |
| US4128543A (en) * | 1977-01-24 | 1978-12-05 | Inolex Corporation | Process for preparing alcohol soluble condensates of abietic acid and a protein hydrolysate |
| US4229429A (en) * | 1978-09-20 | 1980-10-21 | Inolex Corporation | Process for preparing alcohol soluble condensates of abietic acid and a protein hydrolsate |
| US4661340A (en) * | 1983-06-06 | 1987-04-28 | Interkemia Vegyipari Gazdasagi Tarsasag | Quail egg based stabilized foam compositions for cosmetic purposes |
| US5071960A (en) * | 1989-09-07 | 1991-12-10 | Hoechst Aktiengesellschaft | High molecular weight protein/fatty acid condensation products which are very well tolerated by the skin and mucosa |
Also Published As
| Publication number | Publication date |
|---|---|
| GB462977A (en) | 1937-03-12 |
| FR795052A (en) | 1936-03-03 |
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