US3149338A - Hair preparations containing a diamide and process of use thereof - Google Patents
Hair preparations containing a diamide and process of use thereof Download PDFInfo
- Publication number
- US3149338A US3149338A US36754A US3675460A US3149338A US 3149338 A US3149338 A US 3149338A US 36754 A US36754 A US 36754A US 3675460 A US3675460 A US 3675460A US 3149338 A US3149338 A US 3149338A
- Authority
- US
- United States
- Prior art keywords
- hair
- alkyl
- diamide
- group
- aqueous
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 title description 10
- 239000003676 hair preparation Substances 0.000 title description 7
- 238000000034 method Methods 0.000 title description 2
- 239000000203 mixture Substances 0.000 claims description 41
- -1 DIAMIDE COMPOUND Chemical class 0.000 claims description 22
- 239000003795 chemical substances by application Substances 0.000 claims description 18
- 210000004761 scalp Anatomy 0.000 claims description 10
- 239000002537 cosmetic Substances 0.000 claims description 9
- 239000002453 shampoo Substances 0.000 description 25
- 125000000217 alkyl group Chemical group 0.000 description 20
- 239000003599 detergent Substances 0.000 description 19
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 19
- 235000014113 dietary fatty acids Nutrition 0.000 description 15
- 239000000194 fatty acid Substances 0.000 description 15
- 229930195729 fatty acid Natural products 0.000 description 15
- 239000001257 hydrogen Substances 0.000 description 15
- 229910052739 hydrogen Inorganic materials 0.000 description 15
- 125000004432 carbon atom Chemical group C* 0.000 description 14
- 230000003370 grooming effect Effects 0.000 description 14
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 13
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 12
- 239000007788 liquid Substances 0.000 description 12
- 238000003756 stirring Methods 0.000 description 10
- 235000019441 ethanol Nutrition 0.000 description 9
- 150000004665 fatty acids Chemical class 0.000 description 9
- 125000002252 acyl group Chemical group 0.000 description 8
- 239000003240 coconut oil Substances 0.000 description 8
- 235000019864 coconut oil Nutrition 0.000 description 8
- 239000006071 cream Substances 0.000 description 8
- 239000002304 perfume Substances 0.000 description 8
- 239000012071 phase Substances 0.000 description 8
- 239000003755 preservative agent Substances 0.000 description 8
- 230000002335 preservative effect Effects 0.000 description 8
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 7
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 7
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 7
- 239000001301 oxygen Substances 0.000 description 7
- 229910052760 oxygen Inorganic materials 0.000 description 7
- 229910052717 sulfur Chemical group 0.000 description 7
- 239000011593 sulfur Chemical group 0.000 description 7
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 6
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
- OHJMTUPIZMNBFR-UHFFFAOYSA-N biuret Chemical compound NC(=O)NC(N)=O OHJMTUPIZMNBFR-UHFFFAOYSA-N 0.000 description 6
- 239000003638 chemical reducing agent Substances 0.000 description 6
- 150000001875 compounds Chemical class 0.000 description 6
- 150000003839 salts Chemical class 0.000 description 6
- 239000000243 solution Substances 0.000 description 6
- 239000002480 mineral oil Substances 0.000 description 5
- 239000000843 powder Substances 0.000 description 5
- 239000000344 soap Substances 0.000 description 5
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 4
- 230000001476 alcoholic effect Effects 0.000 description 4
- 125000003118 aryl group Chemical group 0.000 description 4
- 150000001470 diamides Chemical class 0.000 description 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 4
- 239000006210 lotion Substances 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 235000010446 mineral oil Nutrition 0.000 description 4
- 239000007787 solid Substances 0.000 description 4
- 235000015961 tonic Nutrition 0.000 description 4
- 230000001256 tonic effect Effects 0.000 description 4
- 229960000716 tonics Drugs 0.000 description 4
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 3
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 3
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- 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 3
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 3
- 239000005642 Oleic acid Substances 0.000 description 3
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 3
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 3
- YCLDXRHGQVDVJR-UHFFFAOYSA-N carbamothioylurea Chemical compound NC(=O)NC(N)=S YCLDXRHGQVDVJR-UHFFFAOYSA-N 0.000 description 3
- 239000000839 emulsion Substances 0.000 description 3
- 235000011187 glycerol Nutrition 0.000 description 3
- SUMDYPCJJOFFON-UHFFFAOYSA-N isethionic acid Chemical compound OCCS(O)(=O)=O SUMDYPCJJOFFON-UHFFFAOYSA-N 0.000 description 3
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 3
- 239000003921 oil Substances 0.000 description 3
- 239000011591 potassium Substances 0.000 description 3
- 229910052700 potassium Inorganic materials 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- 239000011734 sodium Substances 0.000 description 3
- 229910052708 sodium Inorganic materials 0.000 description 3
- 150000005846 sugar alcohols Polymers 0.000 description 3
- LDVVTQMJQSCDMK-UHFFFAOYSA-N 1,3-dihydroxypropan-2-yl formate Chemical compound OCC(CO)OC=O LDVVTQMJQSCDMK-UHFFFAOYSA-N 0.000 description 2
- UOLKUOBCZVAOEZ-UHFFFAOYSA-N 1,3-dimethyl-1-(methylcarbamoyl)urea Chemical compound CNC(=O)N(C)C(=O)NC UOLKUOBCZVAOEZ-UHFFFAOYSA-N 0.000 description 2
- YIOAZBCJHAZGHU-UHFFFAOYSA-N 1-(hydroxymethyl)-3-(hydroxymethylcarbamoyl)urea Chemical compound OCNC(=O)NC(=O)NCO YIOAZBCJHAZGHU-UHFFFAOYSA-N 0.000 description 2
- BEVVHEBDWYSLRT-UHFFFAOYSA-N 1-methyl-3-(methylcarbamoyl)urea Chemical compound CNC(=O)NC(=O)NC BEVVHEBDWYSLRT-UHFFFAOYSA-N 0.000 description 2
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 2
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 2
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 2
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 2
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
- DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 2
- 125000000129 anionic group Chemical group 0.000 description 2
- MWPLVEDNUUSJAV-UHFFFAOYSA-N anthracene Chemical compound C1=CC=CC2=CC3=CC=CC=C3C=C21 MWPLVEDNUUSJAV-UHFFFAOYSA-N 0.000 description 2
- 239000003125 aqueous solvent Substances 0.000 description 2
- 235000013871 bee wax Nutrition 0.000 description 2
- 229940092738 beeswax Drugs 0.000 description 2
- 239000012166 beeswax Substances 0.000 description 2
- UCMIRNVEIXFBKS-UHFFFAOYSA-N beta-alanine Chemical compound NCCC(O)=O UCMIRNVEIXFBKS-UHFFFAOYSA-N 0.000 description 2
- 239000004359 castor oil Substances 0.000 description 2
- 235000019438 castor oil Nutrition 0.000 description 2
- HVYWMOMLDIMFJA-DPAQBDIFSA-N cholesterol Chemical compound C1C=C2C[C@@H](O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@H]([C@H](C)CCCC(C)C)[C@@]1(C)CC2 HVYWMOMLDIMFJA-DPAQBDIFSA-N 0.000 description 2
- 238000004040 coloring Methods 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 2
- 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 2
- BXWNKGSJHAJOGX-UHFFFAOYSA-N hexadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCO BXWNKGSJHAJOGX-UHFFFAOYSA-N 0.000 description 2
- 230000002209 hydrophobic effect Effects 0.000 description 2
- HQKMJHAJHXVSDF-UHFFFAOYSA-L magnesium stearate Chemical compound [Mg+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O HQKMJHAJHXVSDF-UHFFFAOYSA-L 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 2
- YNPNZTXNASCQKK-UHFFFAOYSA-N phenanthrene Chemical compound C1=CC=C2C3=CC=CC=C3C=CC2=C1 YNPNZTXNASCQKK-UHFFFAOYSA-N 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 235000019333 sodium laurylsulphate Nutrition 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 125000001424 substituent group Chemical group 0.000 description 2
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 2
- 239000000271 synthetic detergent Substances 0.000 description 2
- XOAAWQZATWQOTB-UHFFFAOYSA-N taurine Chemical compound NCCS(O)(=O)=O XOAAWQZATWQOTB-UHFFFAOYSA-N 0.000 description 2
- 239000008096 xylene Substances 0.000 description 2
- ALSTYHKOOCGGFT-KTKRTIGZSA-N (9Z)-octadecen-1-ol Chemical compound CCCCCCCC\C=C/CCCCCCCCO ALSTYHKOOCGGFT-KTKRTIGZSA-N 0.000 description 1
- DLQKEOSHQYAJHO-UHFFFAOYSA-M 1-pyridin-1-ium-1-yldodecan-1-one;bromide Chemical compound [Br-].CCCCCCCCCCCC(=O)[N+]1=CC=CC=C1 DLQKEOSHQYAJHO-UHFFFAOYSA-M 0.000 description 1
- WGIMXKDCVCTHGW-UHFFFAOYSA-N 2-(2-hydroxyethoxy)ethyl dodecanoate Chemical compound CCCCCCCCCCCC(=O)OCCOCCO WGIMXKDCVCTHGW-UHFFFAOYSA-N 0.000 description 1
- QTWJRLJHJPIABL-UHFFFAOYSA-N 2-methylphenol;3-methylphenol;4-methylphenol Chemical compound CC1=CC=C(O)C=C1.CC1=CC=CC(O)=C1.CC1=CC=CC=C1O QTWJRLJHJPIABL-UHFFFAOYSA-N 0.000 description 1
- CVZYWFZBNHBFDS-UHFFFAOYSA-N 3-(dodecylamino)propanoate;tris(2-hydroxyethyl)azanium Chemical compound OCCN(CCO)CCO.CCCCCCCCCCCCNCCC(O)=O CVZYWFZBNHBFDS-UHFFFAOYSA-N 0.000 description 1
- YPFUJZAAZJXMIP-UHFFFAOYSA-N 3-sulfopropanediol Chemical compound OCC(O)CS(O)(=O)=O YPFUJZAAZJXMIP-UHFFFAOYSA-N 0.000 description 1
- HIQIXEFWDLTDED-UHFFFAOYSA-N 4-hydroxy-1-piperidin-4-ylpyrrolidin-2-one Chemical compound O=C1CC(O)CN1C1CCNCC1 HIQIXEFWDLTDED-UHFFFAOYSA-N 0.000 description 1
- 241000272189 Accipiter gentilis Species 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- 241000416162 Astragalus gummifer Species 0.000 description 1
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 1
- ZXCSKAQTVNVFFQ-UHFFFAOYSA-N CN(C(=O)N(C(=O)NC)C)C(C)=O Chemical compound CN(C(=O)N(C(=O)NC)C)C(C)=O ZXCSKAQTVNVFFQ-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 1
- 239000004166 Lanolin Substances 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- FSUDRRYQPAXOKG-UHFFFAOYSA-N N-methyl-N-(methylcarbamoylcarbamoyl)acetamide Chemical compound CN(C(=O)NC(=O)NC)C(C)=O FSUDRRYQPAXOKG-UHFFFAOYSA-N 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 235000019482 Palm oil Nutrition 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 1
- 229920001800 Shellac Polymers 0.000 description 1
- BCKXLBQYZLBQEK-KVVVOXFISA-M Sodium oleate Chemical compound [Na+].CCCCCCCC\C=C/CCCCCCCC([O-])=O BCKXLBQYZLBQEK-KVVVOXFISA-M 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical class OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 1
- 229920001615 Tragacanth Polymers 0.000 description 1
- XOCUXOWLYLLJLV-UHFFFAOYSA-N [O].[S] Chemical group [O].[S] XOCUXOWLYLLJLV-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000011149 active material Substances 0.000 description 1
- 239000002671 adjuvant Substances 0.000 description 1
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
- 150000001447 alkali salts Chemical class 0.000 description 1
- 230000029936 alkylation Effects 0.000 description 1
- 238000005804 alkylation reaction Methods 0.000 description 1
- 125000002947 alkylene group Chemical group 0.000 description 1
- 150000003863 ammonium salts Chemical class 0.000 description 1
- 230000000844 anti-bacterial effect Effects 0.000 description 1
- 239000008346 aqueous phase Substances 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- 239000003899 bactericide agent Substances 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 229910021538 borax Inorganic materials 0.000 description 1
- 239000000872 buffer Substances 0.000 description 1
- 239000000920 calcium hydroxide Substances 0.000 description 1
- 235000011116 calcium hydroxide Nutrition 0.000 description 1
- JIRRNZWTWJGJCT-UHFFFAOYSA-N carbamothioylthiourea Chemical compound NC(=S)NC(N)=S JIRRNZWTWJGJCT-UHFFFAOYSA-N 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 125000002091 cationic group Chemical class 0.000 description 1
- 229960000541 cetyl alcohol Drugs 0.000 description 1
- 229940080284 cetyl sulfate Drugs 0.000 description 1
- YMKDRGPMQRFJGP-UHFFFAOYSA-M cetylpyridinium chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCC[N+]1=CC=CC=C1 YMKDRGPMQRFJGP-UHFFFAOYSA-M 0.000 description 1
- 229960001927 cetylpyridinium chloride Drugs 0.000 description 1
- WOWHHFRSBJGXCM-UHFFFAOYSA-M cetyltrimethylammonium chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCC[N+](C)(C)C WOWHHFRSBJGXCM-UHFFFAOYSA-M 0.000 description 1
- 235000012000 cholesterol Nutrition 0.000 description 1
- 229940107161 cholesterol Drugs 0.000 description 1
- 238000005352 clarification Methods 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 229930003836 cresol Natural products 0.000 description 1
- 125000002704 decyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- ILRSCQWREDREME-UHFFFAOYSA-N dodecanamide Chemical compound CCCCCCCCCCCC(N)=O ILRSCQWREDREME-UHFFFAOYSA-N 0.000 description 1
- MOTZDAYCYVMXPC-UHFFFAOYSA-N dodecyl hydrogen sulfate Chemical compound CCCCCCCCCCCCOS(O)(=O)=O MOTZDAYCYVMXPC-UHFFFAOYSA-N 0.000 description 1
- 229940043264 dodecyl sulfate Drugs 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 238000004043 dyeing Methods 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 239000003925 fat Substances 0.000 description 1
- 235000019197 fats Nutrition 0.000 description 1
- 150000002191 fatty alcohols Chemical class 0.000 description 1
- 238000005194 fractionation Methods 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- 239000000118 hair dye Substances 0.000 description 1
- LPTIRUACFKQDHZ-UHFFFAOYSA-N hexadecyl sulfate;hydron Chemical compound CCCCCCCCCCCCCCCCOS(O)(=O)=O LPTIRUACFKQDHZ-UHFFFAOYSA-N 0.000 description 1
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 239000005556 hormone Substances 0.000 description 1
- 229940088597 hormone Drugs 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- AYSSEJBVZOIEGY-UHFFFAOYSA-N hydroxymethylcarbamothioylurea Chemical compound OCNC(=S)NC(=O)N AYSSEJBVZOIEGY-UHFFFAOYSA-N 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 229940045996 isethionic acid Drugs 0.000 description 1
- 229940074928 isopropyl myristate Drugs 0.000 description 1
- 239000004922 lacquer Substances 0.000 description 1
- 235000019388 lanolin Nutrition 0.000 description 1
- 229940039717 lanolin Drugs 0.000 description 1
- 239000007791 liquid phase Substances 0.000 description 1
- 229910003002 lithium salt Inorganic materials 0.000 description 1
- 159000000002 lithium salts Chemical class 0.000 description 1
- 239000002932 luster Substances 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 235000019359 magnesium stearate Nutrition 0.000 description 1
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 1
- 235000019341 magnesium sulphate Nutrition 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 235000010755 mineral Nutrition 0.000 description 1
- 150000005673 monoalkenes Chemical class 0.000 description 1
- TUTVFTIULDRFDP-UHFFFAOYSA-N n-(carbamoylcarbamothioyl)acetamide Chemical compound CC(=O)NC(=S)NC(N)=O TUTVFTIULDRFDP-UHFFFAOYSA-N 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical class [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- 125000001400 nonyl 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])[H] 0.000 description 1
- 239000007764 o/w emulsion Substances 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
- 125000002347 octyl 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])[H] 0.000 description 1
- 235000019198 oils Nutrition 0.000 description 1
- 229940055577 oleyl alcohol Drugs 0.000 description 1
- XMLQWXUVTXCDDL-UHFFFAOYSA-N oleyl alcohol Natural products CCCCCCC=CCCCCCCCCCCO XMLQWXUVTXCDDL-UHFFFAOYSA-N 0.000 description 1
- 239000002540 palm oil Substances 0.000 description 1
- 239000006072 paste Substances 0.000 description 1
- 230000000737 periodic effect Effects 0.000 description 1
- 150000008379 phenol ethers Chemical class 0.000 description 1
- 235000021317 phosphate Nutrition 0.000 description 1
- 239000000419 plant extract Substances 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 238000012552 review Methods 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 230000028327 secretion Effects 0.000 description 1
- 239000004208 shellac Substances 0.000 description 1
- 229940113147 shellac Drugs 0.000 description 1
- 235000013874 shellac Nutrition 0.000 description 1
- 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 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- BTURAGWYSMTVOW-UHFFFAOYSA-M sodium dodecanoate Chemical compound [Na+].CCCCCCCCCCCC([O-])=O BTURAGWYSMTVOW-UHFFFAOYSA-M 0.000 description 1
- 229940082004 sodium laurate Drugs 0.000 description 1
- 229940045870 sodium palmitate Drugs 0.000 description 1
- 239000004328 sodium tetraborate Substances 0.000 description 1
- 235000010339 sodium tetraborate Nutrition 0.000 description 1
- HLWRUJAIJJEZDL-UHFFFAOYSA-M sodium;2-[2-[bis(carboxymethyl)amino]ethyl-(carboxymethyl)amino]acetate Chemical compound [Na+].OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC([O-])=O HLWRUJAIJJEZDL-UHFFFAOYSA-M 0.000 description 1
- GGXKEBACDBNFAF-UHFFFAOYSA-M sodium;hexadecanoate Chemical compound [Na+].CCCCCCCCCCCCCCCC([O-])=O GGXKEBACDBNFAF-UHFFFAOYSA-M 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 239000007790 solid phase Substances 0.000 description 1
- 239000012265 solid product Substances 0.000 description 1
- 239000002195 soluble material Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- SFVFIFLLYFPGHH-UHFFFAOYSA-M stearalkonium chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCCCC[N+](C)(C)CC1=CC=CC=C1 SFVFIFLLYFPGHH-UHFFFAOYSA-M 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
- 150000003460 sulfonic acids Chemical class 0.000 description 1
- 239000003760 tallow Substances 0.000 description 1
- 229960003080 taurine Drugs 0.000 description 1
- 235000013343 vitamin Nutrition 0.000 description 1
- 239000011782 vitamin Substances 0.000 description 1
- 229940088594 vitamin Drugs 0.000 description 1
- 229930003231 vitamin Natural products 0.000 description 1
- 239000007762 w/o emulsion Substances 0.000 description 1
- 230000003442 weekly effect Effects 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
- A61Q5/02—Preparations for cleaning 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
- A61K8/40—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
- A61K8/42—Amides
Definitions
- the present invention relates to a cosmetic composition suitable for daily use in the care of the hair. More particularly it relates to hair cleansing and grooming compositions such as hair lotions, tonics, shampoos and the like which may be used in the daily toilet.
- a cosmetic composition suitable for daily use in the care of the hair and scalp comprises a substantially non-volatile organic toilet agent for the daily care of the hair and a diamide compound having the formula wherein X is selected from the group consisting of oxygen sulfur, R R R and R are selected from the group consisting of hydrogen alkyl, alkylol and acyl, and R is selected from the group consisting of hydrogen and alkyl, said R R R R and R containing up to two carbon atoms each, and from 40 to 99.45% of a volatile aqueous solvent medium, said composition having a pH of from 4 to and being free of reducing agents.
- Suitable such compounds include biuret, thiobiuret, dithiobiuret, and their waterand alcohol-soluble monoand polyalkyl, -alkylol and -acyl derivatives wherein the alkyl, alkylol and acyl groups have in general not more than 2 carbon atoms, e.g.
- l-rnethyl-biuret S-methylbiuret, l-ethyl-biuret, 1,5-dimethyl-biuret, 1,3,5-trimethylbiuret, l-hydroxymethyl-biuret, 1,5-dihydroxymethyl-biuret, I-acetyl-biuret, 1-forrnyl5-acetyl-biuret, 1,5-dimethyl-l-acetyl-biuret, 1,3,5-trimethyl-l-acetyl-biuret, 3-ethyll-acetyl-biuret, l-methyl-thiobiuret, l-ethyl-thiobiuret, 1 acetyl-thiobiuret, 1 hydroxymethyl-thiobiuret, and l-methyl-dithiobiuret.
- the cosmetic compositions of the present invention may be prepared in a wide variety of physical forms. They may be liquids, pastes or solids and may consist of one or more phases. They may, for example, constitute a single aqueous or aqueous-alcoholic phase, or may comprise an aqueous and a separate oily phase as in two layer systems or emulsions of the water-in-oil or oil-inwater types.
- compositions and their constituents are skin-compatible, being suitable for periodic use at short, i.e. daily or at the most weekly, intervals, as distinguished from decorative or treating compositions such as hair dye ing or waving compositions which can be used only at much greater intervals.
- the present cosmetic compositions may be prepared in the form of daily hair grooming products such as hair 10- tions, hair dressings, hair tonics and the like, or they may be prepared in the form of hair cleansing products such as shampoos, the non-volatile organic toilet agent for daily care of the hair being present in each instance in an amount from 0.5 to 98% by Weight of the composition.
- the nonvolatile organic toilet agent for the daily care of the hair stituent containing 8 to 26 carbon atoms.
- Such hair groonnng agents include, e.g., castor oil, mineral o1l, lower alkoxypolyoxy lower alkylene glycols such as butoxypolyoxypropylene glycol, higher molecular weight copolymers of random mixtures of ethylene oxide and propylene oxide, esters of fatty acids such as isopropylmyristate or the coconut oil fatty acid ester of polyethylene glycol having an average molecular Weight of about 400, polyhydric alcohols such as glycerol and propylene glycol, gums such as gum tragacanth, lacquers such as shellac, and the like.
- castor oil mineral o1l
- lower alkoxypolyoxy lower alkylene glycols such as butoxypolyoxypropylene glycol
- higher molecular weight copolymers of random mixtures of ethylene oxide and propylene oxide esters of fatty acids such as isopropylmyristate or the coconut oil fatty acid ester of polyethylene glycol
- substantially non-volatile organic hair grooming agents which have a molecular weight greater than about and preferably greater than about 200 and which contain an alcoholic hydroxyl group such as the aforementioned glycols, polyhydric alcohols, polymerized alkylene oxides, and castor oil.
- the foregoing organic hair grooming materials desirably are employed in the instant hair grooming preparations in an amount from 0.5 to 50% and higher depending on the nature of the respective compound and its compatibility in the desired system.
- the non-volatile organic toilet agent for the daily care of the hair is a cleansing agent such as a water-soluble organic detergent.
- a cleansing agent such as a water-soluble organic detergent.
- this detergent is an anionic sulfate or sulfonate, i.e. a sulfated or sulfonated compound having a hydrophobic substituent containing 8 to 26 carbon atoms, desirably from 12 to 18 carbon atoms, per molecule.
- Detergents of this preferred type which may be suitably employed include the sulfuric acid esters of polyhydric alcohols incompletely esterified with higher fatty acids, e.g., coconut oil monoglyceride monosulfate and fallow diglyceride monosulfate; the long chain'pure or mixed'allryl sulfates such as lauryl sulfate, cetyl sulfate, and higher fatty alcohol sulfates derived from coconut oil; the hydroxy sulfonated higher fatty acid esters such as, e.g., higher fatty acid esters of 2,3-dihydroxypropane sulfonic acid; the lugher fatty acid esters of low molecular weight alkyiolsulfonic acids, e.g., oleic acid ester of isethionic acid; the sulfated higher fatty acid alkylolamides such as, e.g., CthSIiOIZLrldC s
- anionic synthetic detergents which may be employed in shampoos are the sulfonic acid salts of alkylated aromatic hydrocarbon compounds having an alkyl sub
- the aromatic portion of the molecule may be monoor polynuclear, e.g., benzene, toluene, Xylene, naphthalene, phenanthrene, anthracene, etc., and may contain other substituents such as hydroxyl groups or short chain alkyl groups such as, e.g., in phenol, cresol, phenol ethers, toluene, Xylene, etc.
- the long chain alkyl substituent of the alkylated aromatic molecule preferably is saturated and may be straight chain or branched.
- Representative long chain alkyl groups include the dodecyl, hexyl, octyl, nonyl, and decyl groups as well as mixed alkyls derived from fatty materials, cracked parafiins or polymers of lower mono olefins, etc.
- the alkylated aromatic detergents employed will be a mixture of compounds having alkyl substituents of varying chain length since the chain length is dependent upon the sharpness of the fractionation of the aliphatic hydrocarbon used for the alkylation.
- the average chain length of the alkyl substituents shouldbe in general from 9 to 15 carbon atoms and preferably between 12 and 14 carbon atoms.
- detergents are employed in shampoos prepared in accordance with the present invention in the form of their water-soluble salts.
- detergents may be used in the form of their alkali salts, e.g.,
- salts of nitrogen containing bases e.g., as salts of low molecular alkylolamines such as mono-, diand triethanolamine, and as mixtures of various of these salts.
- anionic detergents which may also be employed include water-soluble alkyl phosphates, sulfated ethylene oxide condensates of hydrophobic materials such as higher fatty acids, fatty alcohols, alkyl aromatic hydrocarbons and the like, sulfonated oils, soaps such as sodium, potassium and triethanolamine soaps of higher fatty acids containing from 12 to 18 carbon atoms as well as mixtures of soaps being especially useful such as sodium laurate, sodium palmitate, sodium oleate and the potassium and/or triethanolamine soaps of coconut oil, palm oil, and tallow fatty acids.
- water-soluble alkyl phosphates sulfated ethylene oxide condensates of hydrophobic materials such as higher fatty acids, fatty alcohols, alkyl aromatic hydrocarbons and the like, sulfonated oils, soaps such as sodium, potassium and triethanolamine soaps of higher fatty acids containing from 12 to 18 carbon atoms as well as mixtures of soaps being especially useful such as sodium laur
- lauroyl pyridinium bromide, cetyl trimethyl ammonium chloride or cetyl pyridinium chloride may also be used alone or'in combination with other compatible detergents.
- Suitable salts of cationic detergents are the chloride, bromide, acetate and sulfate.
- Suitable detergents are furthermore the amphoteric detergents such as salts of the N-alkyl compounds of betaamino propionic acid wherein the alkyl group is derived from a fatty acid fatty acids.
- Shampoos in accordance with the present invention may be prepared in any convenient physical form and may consist of one or more phases.
- a shampoo such as the mixture of coconut oil 'may be a solid product such as a bar or a powder, or a clear, homogeneous single phase liquid such as an aqueous or aqueous-alcoholic composition, or it may contain two or more liquid or mixed liquid and solid phases, as in ably comprise 'at least and prferably from to 40% "of the instant shampoos when they are prepared in a liquid or paste formQand from 15 to 98% when the shampoo is prepared in the form of a solid'composition;
- an'aqueous cosmetic composition may comprise from 0.05 to 10% of diamide, from 0.5 to 50% of the non-volatile organic toilet agent, and as the balance,
- a volatile aqueous solvent medium such as water or mixtures of water and a lower monohydric alcohol such as ethanol or isopropyl alcohol.
- a clear, homogeneous single phase aqueous shampoo preferably 0.5 to 2% of one of the instant diamide compounds, 5 to 20% water soluble detergent, and 7894.5% water and other components are used, Whereas in a shampoo containing aqueous alcohol wherein said diamide compounds and detergents are each more soluble, more than 2% of the diamide may be used in combination with 5 to 40% of the detergent, the balance being aqueous alcohol and other components.
- solid, powder or cream shampoos amounts of 0.05 up to 10% of diamide are possible in combination with 15 to 98% of the detergent and'a balance of water and/ or other components.
- the instant hair preparations may also contain as adjuvant materials various substances such as vitamins, hormones, cholesterol, lanolin, bactericides, plant extracts, buffers, and the like in compatible proportions, although the preparations should be free of substantial quantities of water insoluble sohd substanceswhich may be deposited on and clog the pores of the scalp.
- the present compositions have a pH of 4 to 10 as they appear to be most effective in this range.
- the hair preparations of the invention exhibit unusua ly excellent hair grooming properties. They render the hair soft and manageable, impart a high gloss and luster, and are particularly effective in controlling or preventing the formation of dry flaky scales of sloughed-oif skin.
- aqueous compositions prepared in accordance with the present invention is favorably infiuenced by the presence of a water soluble material which reduces the surfaceand/or interfacialatension of water (e.g. alcohol in alcoholic hair tonics, soaps or synthetic detergents in shampoos, emulsifiers in hair dressings).
- a water soluble material which reduces the surfaceand/or interfacialatension of water
- the presence of these surface active materials is believed to reduce the interfacial tension between the aqueous phase containing the instant water soluble diamides and the hair v and scalp so that soil and oily secretions are more easily temperature or elevated temperature in the amount of water, alcohol or aqueous alcohol required for the respective hair preparation.
- the toilet agent for the daily care of the hair may be added in the usual way, i.e.
- liquid shampoos or hair rinses the hair grooming agent may be added to the liquid containing the diamide of the invention, and in the case of hair creams of the oil-in-water or water-in-oil type, the
- liquid containing the diamide may be heated to 50-70 C. and emulsified with the molten fats, mineral oils orlike hair grooming agents, the emulsion, if necessary, being homogenized thereafter.
- Cream shampoos formulated in accordance with the present invention may be prepared by mixing an aqueous detergent paste with an appropriate diamide compound and any other desired components with stirring at an elevated temperature (4060 C.).
- Powder shampoos may be made by homogeneously mixing the desired components in a mixer.
- the hair lotions of Examples 2 and 3 are prepared in a Way analogous to Example 1.
- EXAMPLE 4 Hair Cream [Oil-imwzxter emulsion] 14 parts of diglycol laurate, 34 parts of mineral oil and 0.2 part of a preservative (e.g. methyl-p-hydroxy benzoic acid ester) are heated to 80 C. This mix is slowly and thoroughly stirred into a solution of 1 part of thiobiuret in 50.5 parts of water. After cooling to 35 C., 0.3 part of perfume is added. Finally the cream is homogenized on a roller mill.
- a preservative e.g. methyl-p-hydroxy benzoic acid ester
- Part I is heated to 6065 C. and slowly added with vigorous stirring to part 11 previously heated to 60-65 C.
- the cream is cooled with stirring to 35 C. at which temperature part III is added.
- Part I is heated to 7075 C. Then part H previously heated to 60 C. is slowly added with thorough stirring, and finally part III is introduced. The cream is stirred at 70 C. for 10 minutes and then slowly cooled with stirring to 55 C. At this temperature, part IV is added. Then the cream is cooled to 35 C. and homogenized at 30 C.
- Part I is heated to C. while stirring. After a homogeneous mix is obtained, part II previously heated to 35 C. is added with cautious stirring and finally part III is introducedf EXAh/IPLE 8 Powder Shampoo Parts Sodium lauryl isethionate 60.0 Sodium bicarbonate 34.5 l-methyl-biuret 5 .0 Perfume 0.5
- the solid components are homogeneously mixed in a mixer and the perfume is added by spraying it on the powder while moving the mass in the mixer.
- EXAMPLE 9 Liquid Shampoo 97.4 parts of an aqueous alcoholic solution containing 20 parts of ammonium coconut oil monoglyceride monosulfate and 20 parts of ethyl alcohol are heated to -35 C. 2 parts of 1,3,5-trimethylbiuret, 0.2 part of preservative, 0.05 part of dyestuff and 0.35 part of perfume are stirred successively into this solution.
- EXAMPLE 10 Liquid Shampoo Parts N-lauryl-beta-amino-propionic acid triethanolamine salt, 40% 50.0
- Cream Shampoo 91.8 parts of an aqueous sodium lauryl sulfate paste containing about 45- parts of sodium lauryl sulfate are heated to 5060 C. To this mix a melt from 2 parts of polyethylene glycol-400-distearate, 1.5 parts of magnesium stearate and 1 part of oleyl alcohol and then 0.2 par-t of a preservative and 3 parts of thiobiuret. are added with stirring. After cooling to 40 C. 0.5 part of perfume is introduced.
- aqueous solution is prepared at room temperature. After standingrfor 24 hours the solution is filtered.
- X is selected from the group consisting of oxygen and sulfur
- R R R and R are selected from the group consisting of hydrogen, alkyl, alkylol and acyl
- R is selected from the group consisting of hydrogen and alkyl, said R R R R and R containing up to two carbon atoms each, and from to 99.45% of a volatile aqueousj solvent medium, said composition having a pH of from 4 to 10 and being freeof reducing agents.
- a shampoo composition comprising from about 5 to 98% of a water soluble organic detergent, and .05 to 10% of a diamide compound having the formula wherein X is selected from the group consisting of oxygen 7 and sulfur, R R R and R are selected from the group 7 consisting of hydrogen, alkyl, alkylol and acyl, and R is selected from the group consisting of hydrogen and alkyl, said R R R R and R containing up to two carbon atoms each, and water as the balance, said composition having a pH of 4 to '10 and being free of reducing agents.
- a hair grooming composition suitable for daily use in the care of the hair'and scalp which comprises about 0.5 to by weight of a substantially non-volatile organic hair grooming agent containing an, alcoholic hydroxyl group and having a molecular weight greater than about '75, 0.05 to 10% of a dianiide compound having the'formula J said R R R R and R containing up to two carbon atoms each, and 40 to 99.45% of a volatile aqueous sol- .ventmedium, said comp ositionihaving a pH oft-4 to 10 and being free of reducing agents. 5
- a process for the treatment of the hair and scalp which comprises the daily application thereto of a substantially non-volatile toilet agent for the daily care of the hair and about 0.05 to 10% by weight of a diamide CO1 pound having the formula wherein X is selected from the group consisting of oxygen and sulfur, R R R and R are selected from the group consisting of hydrogen, alkyl, alkylol and aryl, and R is selected from the group consisting of hydrogen and alkyl, said R R R R and R containing up to two carbon atoms each, the said toilet agent and diamide compound being applied to the hair and scalp at a pH of 4 .to 10.
- a cosmetic composition suitable for daily use in the care of the hair and scalp which comprises a substantially non-volatile toilet agent for the daily care of the hair and from about 0.25 to 2.0% by weight of a diamide compound having the formula wherein X is selected from the group consisting of oxygen and sulfur, R R R and R are selected from the group consisting of hydrogen, alkyl, alkylol and acyl, and R is selected from the group consisting ofhydrogen and alkyl, said R R R R and R containing up to two carbon atoms each, said composition having a pH of 4 to 10 when disposed in an aqueous liquid and being free of reducing agents.
- a cosmetic composition suitable. for daily use in the care of the hair and scalp which comprises a substantially non-volatile toilet agent for the daily care of the hair and from about 0.25 to 1.0% by weight of a diamide com pound having the formula wherein X is selected from the group consisting of oxygen and sulfur, R R R and R are selected from the group consisting of hydrogen, alkyl, alkylol and acyl, and R is selected from the group consisting and hydrogen and 'alkyl, V
- X is selected from the group consisting of oxygen and sulfur
- R R R and R are selected from the group consisting of hydrogen, alkyl, alkylol and acyl
- R is selected from the group consisting of hydrogen and alkyl, said R R ,”R R and R containing up, to two carbon atoms each, said composition having a pH of 4 to 10 when disposed in an aqueous liquid and being free of reducing agents.
- A' hair groom ng composition suitable for daily use in the careof the hair and scalp which comprises about;
- X is selected from the group consisting of oxygen 75 320 N th 1 d Jul 15 1954 and sulfur
- R R R and R are selected from the group 6 er an s n y consisting of hydrogen, alkyl, alkylol and acyl
- R is 10
- OTHER REFERENCES selected from the group consisting of hydrogen 311d y Kurzer: Chemical Reviews, vol. 56, pages 95 to 197, said R R R R and R containing up to two carbon February-June 1956. atoms each, and 40 to 99.45% of a volatile aqueous sol- Harry: Modern Cosmeticology, vol. 1, Fourth edition,
- vent medium said composition having a pH of 4 to 10. published by Leonard Hill Ltd., 1955, pages 432 to 434.
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Description
- Patented Sept. 15, 1964 3,149,338 HAIR iREPARATEflNS QGNTAHQTNG A DEAD/HER AND PRG-CESS 43F USE TE EREQF Loin Habicht, Aumuhle, near Hamburg, and Arno Kluge,
Bad Sorlen, Taunus, Germany, assignors to Qolgate- Palmolive Company, New York, N.Y., a corporation of Delaware No Drawing. Filed lune 17, 1960, Ser. No. 36,754 (Ilaims priority, application Germany, duly 7, 1959, P 23,1tl2 11 Claims. (Cl. l6787) The present invention relates to a cosmetic composition suitable for daily use in the care of the hair. More particularly it relates to hair cleansing and grooming compositions such as hair lotions, tonics, shampoos and the like which may be used in the daily toilet.
in accordance with the present invention a cosmetic composition suitable for daily use in the care of the hair and scalp comprises a substantially non-volatile organic toilet agent for the daily care of the hair and a diamide compound having the formula wherein X is selected from the group consisting of oxygen sulfur, R R R and R are selected from the group consisting of hydrogen alkyl, alkylol and acyl, and R is selected from the group consisting of hydrogen and alkyl, said R R R R and R containing up to two carbon atoms each, and from 40 to 99.45% of a volatile aqueous solvent medium, said composition having a pH of from 4 to and being free of reducing agents. Suitable such compounds include biuret, thiobiuret, dithiobiuret, and their waterand alcohol-soluble monoand polyalkyl, -alkylol and -acyl derivatives wherein the alkyl, alkylol and acyl groups have in general not more than 2 carbon atoms, e.g. l-rnethyl-biuret, S-methylbiuret, l-ethyl-biuret, 1,5-dimethyl-biuret, 1,3,5-trimethylbiuret, l-hydroxymethyl-biuret, 1,5-dihydroxymethyl-biuret, I-acetyl-biuret, 1-forrnyl5-acetyl-biuret, 1,5-dimethyl-l-acetyl-biuret, 1,3,5-trimethyl-l-acetyl-biuret, 3-ethyll-acetyl-biuret, l-methyl-thiobiuret, l-ethyl-thiobiuret, 1 acetyl-thiobiuret, 1 hydroxymethyl-thiobiuret, and l-methyl-dithiobiuret.
The cosmetic compositions of the present invention may be prepared in a wide variety of physical forms. They may be liquids, pastes or solids and may consist of one or more phases. They may, for example, constitute a single aqueous or aqueous-alcoholic phase, or may comprise an aqueous and a separate oily phase as in two layer systems or emulsions of the water-in-oil or oil-inwater types.
The instant compositions and their constituents are skin-compatible, being suitable for periodic use at short, i.e. daily or at the most weekly, intervals, as distinguished from decorative or treating compositions such as hair dye ing or waving compositions which can be used only at much greater intervals. Thus it is contemplated that the present cosmetic compositions may be prepared in the form of daily hair grooming products such as hair 10- tions, hair dressings, hair tonics and the like, or they may be prepared in the form of hair cleansing products such as shampoos, the non-volatile organic toilet agent for daily care of the hair being present in each instance in an amount from 0.5 to 98% by Weight of the composition.
In the case of hair grooming compositions, the nonvolatile organic toilet agent for the daily care of the hair stituent containing 8 to 26 carbon atoms.
is an agent which facilitates grooming of the hair and helps to keep the hair in place. Such hair groonnng agents include, e.g., castor oil, mineral o1l, lower alkoxypolyoxy lower alkylene glycols such as butoxypolyoxypropylene glycol, higher molecular weight copolymers of random mixtures of ethylene oxide and propylene oxide, esters of fatty acids such as isopropylmyristate or the coconut oil fatty acid ester of polyethylene glycol having an average molecular Weight of about 400, polyhydric alcohols such as glycerol and propylene glycol, gums such as gum tragacanth, lacquers such as shellac, and the like. It is preferred to employ those substantially non-volatile organic hair grooming agents which have a molecular weight greater than about and preferably greater than about 200 and which contain an alcoholic hydroxyl group such as the aforementioned glycols, polyhydric alcohols, polymerized alkylene oxides, and castor oil. The foregoing organic hair grooming materials desirably are employed in the instant hair grooming preparations in an amount from 0.5 to 50% and higher depending on the nature of the respective compound and its compatibility in the desired system.
In the case of hair cleansing compositions or shampoos, the non-volatile organic toilet agent for the daily care of the hair is a cleansing agent such as a water-soluble organic detergent. Preferably this detergent is an anionic sulfate or sulfonate, i.e. a sulfated or sulfonated compound having a hydrophobic substituent containing 8 to 26 carbon atoms, desirably from 12 to 18 carbon atoms, per molecule.
Detergents of this preferred type which may be suitably employed include the sulfuric acid esters of polyhydric alcohols incompletely esterified with higher fatty acids, e.g., coconut oil monoglyceride monosulfate and fallow diglyceride monosulfate; the long chain'pure or mixed'allryl sulfates such as lauryl sulfate, cetyl sulfate, and higher fatty alcohol sulfates derived from coconut oil; the hydroxy sulfonated higher fatty acid esters such as, e.g., higher fatty acid esters of 2,3-dihydroxypropane sulfonic acid; the lugher fatty acid esters of low molecular weight alkyiolsulfonic acids, e.g., oleic acid ester of isethionic acid; the sulfated higher fatty acid alkylolamides such as, e.g., CthSIiOIZLrldC sulfates; the higher fatty acid amides of amino alkyl sulfonic acids, e.g., the lauric amide of taurine, and the like.
Other anionic synthetic detergents which may be employed in shampoos are the sulfonic acid salts of alkylated aromatic hydrocarbon compounds having an alkyl sub The aromatic portion of the molecule may be monoor polynuclear, e.g., benzene, toluene, Xylene, naphthalene, phenanthrene, anthracene, etc., and may contain other substituents such as hydroxyl groups or short chain alkyl groups such as, e.g., in phenol, cresol, phenol ethers, toluene, Xylene, etc. The long chain alkyl substituent of the alkylated aromatic molecule preferably is saturated and may be straight chain or branched. Representative long chain alkyl groups include the dodecyl, hexyl, octyl, nonyl, and decyl groups as well as mixed alkyls derived from fatty materials, cracked parafiins or polymers of lower mono olefins, etc. In general, the alkylated aromatic detergents employed will be a mixture of compounds having alkyl substituents of varying chain length since the chain length is dependent upon the sharpness of the fractionation of the aliphatic hydrocarbon used for the alkylation. The average chain length of the alkyl substituents shouldbe in general from 9 to 15 carbon atoms and preferably between 12 and 14 carbon atoms.
These various anionic detergents are employed in shampoos prepared in accordance with the present invention in the form of their water-soluble salts. Thus, detergents may be used in the form of their alkali salts, e.g.,
as sodium, potassium or lithium salts, or as ammonium salts, as well as in the form of salts of nitrogen containing bases, e.g., as salts of low molecular alkylolamines such as mono-, diand triethanolamine, and as mixtures of various of these salts.
Other anionic detergents which may also be employed include water-soluble alkyl phosphates, sulfated ethylene oxide condensates of hydrophobic materials such as higher fatty acids, fatty alcohols, alkyl aromatic hydrocarbons and the like, sulfonated oils, soaps such as sodium, potassium and triethanolamine soaps of higher fatty acids containing from 12 to 18 carbon atoms as well as mixtures of soaps being especially useful such as sodium laurate, sodium palmitate, sodium oleate and the potassium and/or triethanolamine soaps of coconut oil, palm oil, and tallow fatty acids.
lauroyl pyridinium bromide, cetyl trimethyl ammonium chloride or cetyl pyridinium chloride may also be used alone or'in combination with other compatible detergents. Suitable salts of cationic detergents are the chloride, bromide, acetate and sulfate. V
Suitable detergents are furthermore the amphoteric detergents such as salts of the N-alkyl compounds of betaamino propionic acid wherein the alkyl group is derived from a fatty acid fatty acids.
Shampoos in accordance with the present invention may be prepared in any convenient physical form and may consist of one or more phases. Thus such a shampoo such as the mixture of coconut oil 'may be a solid product such as a bar or a powder, or a clear, homogeneous single phase liquid such as an aqueous or aqueous-alcoholic composition, or it may contain two or more liquid or mixed liquid and solid phases, as in ably comprise 'at least and prferably from to 40% "of the instant shampoos when they are prepared in a liquid or paste formQand from 15 to 98% when the shampoo is prepared in the form of a solid'composition;
The diamide compounds of the present invention constitute a minor proportion, on the order of 0.05 to 10% of the instant hair preparations, the most suitable amount depending on the characteristics desired; Thus, in a clear, homogeneous, single phase,.aqueous type of hair preparation preferably an amount on the order of 0.25 to 'the case of cream-shampoos, lotion-shampoos, pasteshampoos, and the like. The foregoing detergents desir- 1.0% of the composition in employed. In a single phase 1 For example, an'aqueous cosmetic composition may comprise from 0.05 to 10% of diamide, from 0.5 to 50% of the non-volatile organic toilet agent, and as the balance,
e. g.14099.45%, a volatile aqueous solvent medium such as water or mixtures of water and a lower monohydric alcohol such as ethanol or isopropyl alcohol. In the reparation of a clear, homogeneous single phase aqueous shampoo, preferably 0.5 to 2% of one of the instant diamide compounds, 5 to 20% water soluble detergent, and 7894.5% water and other components are used, Whereas in a shampoo containing aqueous alcohol wherein said diamide compounds and detergents are each more soluble, more than 2% of the diamide may be used in combination with 5 to 40% of the detergent, the balance being aqueous alcohol and other components. In solid, powder or cream shampoos amounts of 0.05 up to 10% of diamide are possible in combination with 15 to 98% of the detergent and'a balance of water and/ or other components.
The instant hair preparations may also contain as adjuvant materials various substances such as vitamins, hormones, cholesterol, lanolin, bactericides, plant extracts, buffers, and the like in compatible proportions, although the preparations should be free of substantial quantities of water insoluble sohd substanceswhich may be deposited on and clog the pores of the scalp. Desirably the present compositions have a pH of 4 to 10 as they appear to be most effective in this range.
The hair preparations of the invention exhibit unusua ly excellent hair grooming properties. They render the hair soft and manageable, impart a high gloss and luster, and are particularly effective in controlling or preventing the formation of dry flaky scales of sloughed-oif skin.
The efiiciency of aqueous compositions prepared in accordance with the present invention is favorably infiuenced by the presence of a water soluble material which reduces the surfaceand/or interfacialatension of water (e.g. alcohol in alcoholic hair tonics, soaps or synthetic detergents in shampoos, emulsifiers in hair dressings). The presence of these surface active materials is believed to reduce the interfacial tension between the aqueous phase containing the instant water soluble diamides and the hair v and scalp so that soil and oily secretions are more easily temperature or elevated temperature in the amount of water, alcohol or aqueous alcohol required for the respective hair preparation. Thereafter, the toilet agent for the daily care of the hair may be added in the usual way, i.e.
in the case of hair tonics, liquid shampoos or hair rinses the hair grooming agent may be added to the liquid containing the diamide of the invention, and in the case of hair creams of the oil-in-water or water-in-oil type, the
liquid containing the diamide may be heated to 50-70 C. and emulsified with the molten fats, mineral oils orlike hair grooming agents, the emulsion, if necessary, being homogenized thereafter.
Cream shampoos formulated in accordance with the present invention may be prepared by mixing an aqueous detergent paste with an appropriate diamide compound and any other desired components with stirring at an elevated temperature (4060 C.)..
Powder shampoos may be made by homogeneously mixing the desired components in a mixer.
. Specific hair preparations according to the invention are illustrated by the following examples. All parts indicated 'areby weight unless otherwise specified.
EXAMPLE 1 v V Hair Lotion To 56 parts of ethyl alcohol 96% and 6 pmts of glycerine 98%- ina suitable mixer 2 parts of biuret are added with stirring. After complete dissolutionof the biuret,
0.19 partof perfume and 0.01 part of dyestuif are introduced as coloring for the lotion, and after short stirring 35.8 parts of deionized waterare added. For clarification 0.1 part of magnesium carbonateis stirred into the solution and filtered oif again.
Water 45 .6
The hair lotions of Examples 2 and 3 are prepared in a Way analogous to Example 1.
EXAMPLE 4 Hair Cream [Oil-imwzxter emulsion] 14 parts of diglycol laurate, 34 parts of mineral oil and 0.2 part of a preservative (e.g. methyl-p-hydroxy benzoic acid ester) are heated to 80 C. This mix is slowly and thoroughly stirred into a solution of 1 part of thiobiuret in 50.5 parts of water. After cooling to 35 C., 0.3 part of perfume is added. Finally the cream is homogenized on a roller mill.
EXAMPLE 5 Hair Cream [Oil-in-water emulsion] Part I Parts Mineral oil 33.0
Beeswax 3.0 Stearic acid 0.5 Cetyl alcohol 1.3 Preservative 0.2
Part II Borax 0.25
Triethanolarnine 1.85 1,5-dihydroxymethyl-biuret 5.00 Water 54.60
Part III Perfume 0.30
Part I is heated to 6065 C. and slowly added with vigorous stirring to part 11 previously heated to 60-65 C. The cream is cooled with stirring to 35 C. at which temperature part III is added.
EXAMPLE 6 Hair Cream [Water-in-oil emulsion] Part I Parts Bees wax n 1.5 Oleic acid 1.0 Mineral oil 40.6 Preservative 0.2
Part II Milk of lime 0.14% 50.0 l-formyl-S-acetyl-biuret 1 .0
Part III Magnesium sulfate solution 10% 5.0
Part IV Perfume 0.7
6 Part I is heated to 7075 C. Then part H previously heated to 60 C. is slowly added with thorough stirring, and finally part III is introduced. The cream is stirred at 70 C. for 10 minutes and then slowly cooled with stirring to 55 C. At this temperature, part IV is added. Then the cream is cooled to 35 C. and homogenized at 30 C.
EXAMPLE 7 Liquid Shampoo Part I Parts Oleic acid 5.0 Coconut oil fatty acid 4.0 Triethanolamine 5.5 Propylene glycol 5.0 Preservative 0.2
Part II Ethylene diamine tetraacetic acid sodium salt 0.5 Biuret 1.5
Water 78.0
Part III Perfume 0.3
Part I is heated to C. while stirring. After a homogeneous mix is obtained, part II previously heated to 35 C. is added with cautious stirring and finally part III is introducedf EXAh/IPLE 8 Powder Shampoo Parts Sodium lauryl isethionate 60.0 Sodium bicarbonate 34.5 l-methyl-biuret 5 .0 Perfume 0.5
The solid components are homogeneously mixed in a mixer and the perfume is added by spraying it on the powder while moving the mass in the mixer.
EXAMPLE 9 Liquid Shampoo 97.4 parts of an aqueous alcoholic solution containing 20 parts of ammonium coconut oil monoglyceride monosulfate and 20 parts of ethyl alcohol are heated to -35 C. 2 parts of 1,3,5-trimethylbiuret, 0.2 part of preservative, 0.05 part of dyestuff and 0.35 part of perfume are stirred successively into this solution.
EXAMPLE 10' Liquid Shampoo Parts N-lauryl-beta-amino-propionic acid triethanolamine salt, 40% 50.0
Coconut oil fatty acid diethanolamide 2.0 1,5-dimethylbiuret 3.0 Perfume, preservative, coloring 0.6 Water 44.4
This composition is prepared in a similar way as described in Example 9.
EXAMPLE 11 Cream Shampoo 91.8 parts of an aqueous sodium lauryl sulfate paste containing about 45- parts of sodium lauryl sulfate are heated to 5060 C. To this mix a melt from 2 parts of polyethylene glycol-400-distearate, 1.5 parts of magnesium stearate and 1 part of oleyl alcohol and then 0.2 par-t of a preservative and 3 parts of thiobiuret. are added with stirring. After cooling to 40 C. 0.5 part of perfume is introduced.
EXAMPLE 12 Hair Rinse 7 Parts Stearyl dimethyl benzyl ammonium chloride 4.0 Polyglycol-400-distearate 3 .0
l-hydroxymethyl-biuret 2.0 Perfume, preservative 0.5
Water 90.5
From all components an aqueous solution is prepared at room temperature. After standingrfor 24 hours the solution is filtered.
Although the present invention has been described with reference to particular embodiments and examples, it
wherein X is selected from the group consisting of oxygen and sulfur, R R R and R are selected from the group consisting of hydrogen, alkyl, alkylol and acyl, and R is selected from the group consisting of hydrogen and alkyl, said R R R R and R containing up to two carbon atoms each, and from to 99.45% of a volatile aqueousj solvent medium, said composition having a pH of from 4 to 10 and being freeof reducing agents.
2. A cosmetic composition as set forth in claim 1 wherein said diamide is biuret.
3. A shampoo composition comprising from about 5 to 98% of a water soluble organic detergent, and .05 to 10% of a diamide compound having the formula wherein X is selected from the group consisting of oxygen 7 and sulfur, R R R and R are selected from the group 7 consisting of hydrogen, alkyl, alkylol and acyl, and R is selected from the group consisting of hydrogen and alkyl, said R R R R and R containing up to two carbon atoms each, and water as the balance, said composition having a pH of 4 to '10 and being free of reducing agents.
4. A shampoo composition as set forth in claim 3 wherein said diamide is biuret.
5. A hair grooming composition suitable for daily use in the care of the hair'and scalp which comprises about 0.5 to by weight of a substantially non-volatile organic hair grooming agent containing an, alcoholic hydroxyl group and having a molecular weight greater than about '75, 0.05 to 10% of a dianiide compound having the'formula J said R R R R and R containing up to two carbon atoms each, and 40 to 99.45% of a volatile aqueous sol- .ventmedium, said comp ositionihaving a pH oft-4 to 10 and being free of reducing agents. 5
6. A hair grooming preparation as set forth in claim 5 wherein said hair grooming agent is glycerine. V
7. A process for the treatment of the hair and scalp which comprises the daily application thereto of a substantially non-volatile toilet agent for the daily care of the hair and about 0.05 to 10% by weight of a diamide CO1 pound having the formula wherein X is selected from the group consisting of oxygen and sulfur, R R R and R are selected from the group consisting of hydrogen, alkyl, alkylol and aryl, and R is selected from the group consisting of hydrogen and alkyl, said R R R R and R containing up to two carbon atoms each, the said toilet agent and diamide compound being applied to the hair and scalp at a pH of 4 .to 10.
8. A cosmetic composition suitable for daily use in the care of the hair and scalp which comprises a substantially non-volatile toilet agent for the daily care of the hair and from about 0.25 to 2.0% by weight of a diamide compound having the formula wherein X is selected from the group consisting of oxygen and sulfur, R R R and R are selected from the group consisting of hydrogen, alkyl, alkylol and acyl, and R is selected from the group consisting ofhydrogen and alkyl, said R R R R and R containing up to two carbon atoms each, said composition having a pH of 4 to 10 when disposed in an aqueous liquid and being free of reducing agents. i
9. A cosmetic composition suitable. for daily use in the care of the hair and scalp which comprises a substantially non-volatile toilet agent for the daily care of the hair and from about 0.25 to 1.0% by weight of a diamide com pound having the formula wherein X is selected from the group consisting of oxygen and sulfur, R R R and R are selected from the group consisting of hydrogen, alkyl, alkylol and acyl, and R is selected from the group consisting and hydrogen and 'alkyl, V
wherein X is selected from the group consisting of oxygen and sulfur, R R R and R are selected from the group consisting of hydrogen, alkyl, alkylol and acyl, and R is selected from the group consisting of hydrogen and alkyl, said R R ,"R R and R containing up, to two carbon atoms each, said composition having a pH of 4 to 10 when disposed in an aqueous liquid and being free of reducing agents. V
11. A' hair groom ng composition suitable for daily use in the careof the hair and scalp which comprises about;
9 10 0.5 to 50% by weight of mineral oil, 0.05 to 10% of 2. References Cited in the file of this patent dialm'de compound having the formula UNITED STATES PATENTS R1\ /R4 2,371,112 Sperry Mar. 6, 1945 2,371,113 Sperry Mar. 6, 1945 OX E 0X 5 2,813,783 Gleim Nov. 19, 1957 FOREIGN PATENTS wherein X is selected from the group consisting of oxygen 75 320 N th 1 d Jul 15 1954 and sulfur, R R R and R are selected from the group 6 er an s n y consisting of hydrogen, alkyl, alkylol and acyl, and R is 10 OTHER REFERENCES selected from the group consisting of hydrogen 311d y Kurzer: Chemical Reviews, vol. 56, pages 95 to 197, said R R R R and R containing up to two carbon February-June 1956. atoms each, and 40 to 99.45% of a volatile aqueous sol- Harry: Modern Cosmeticology, vol. 1, Fourth edition,
vent medium, said composition having a pH of 4 to 10. published by Leonard Hill Ltd., 1955, pages 432 to 434.
Claims (1)
1. AN AQUEOUS COSMETIC COMPOSITION SUITALBE FOR DAILY USE IN THE CARE OF THE HAIR AND SCALP WHICH COMPRISES ABOUT 0.5 TO 50% BY WEIGHT OF A SUBSTANTIALLY NON-VOLATILE ORGANIC TOILET AGENT FOR THE CARE OF THE HAIR, ABOUT 0.05 TO 10% OF A DIAMIDE COMPOUND HAVING THE FORMULA
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE3149338X | 1959-07-07 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US3149338A true US3149338A (en) | 1964-09-15 |
Family
ID=8087855
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US36754A Expired - Lifetime US3149338A (en) | 1959-07-07 | 1960-06-17 | Hair preparations containing a diamide and process of use thereof |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US3149338A (en) |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3725525A (en) * | 1970-07-01 | 1973-04-03 | B Joos | Hair and nail hardening process |
| US3950366A (en) * | 1973-05-10 | 1976-04-13 | Hercules Incorporated | Metal salts of 1,1,5,5-tetrasubstituted dithiobiurets |
| US3988438A (en) * | 1975-01-10 | 1976-10-26 | American Cyanamid Company | Hair conditioning shampoo |
| US4011318A (en) * | 1973-05-10 | 1977-03-08 | Hercules Incorporated | Metal salts of 1,1,5,5-tetrasubstituted dithiobiurets as population control agents |
| US4293713A (en) * | 1979-03-31 | 1981-10-06 | Taiho Pharmaceutical Company Limited | Novel 1,1,3,5-substituted biuret compound and a pharmaceutical composition containing the same |
Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NL75320C (en) * | ||||
| US2371112A (en) * | 1945-03-06 | Dithiobiuret xnd method of | ||
| US2371113A (en) * | 1945-03-06 | Method of preparing monothiobibret | ||
| US2813783A (en) * | 1953-05-18 | 1957-11-19 | Universal Oil Prod Co | Stabilization of organic compounds |
-
1960
- 1960-06-17 US US36754A patent/US3149338A/en not_active Expired - Lifetime
Patent Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NL75320C (en) * | ||||
| US2371112A (en) * | 1945-03-06 | Dithiobiuret xnd method of | ||
| US2371113A (en) * | 1945-03-06 | Method of preparing monothiobibret | ||
| US2813783A (en) * | 1953-05-18 | 1957-11-19 | Universal Oil Prod Co | Stabilization of organic compounds |
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3725525A (en) * | 1970-07-01 | 1973-04-03 | B Joos | Hair and nail hardening process |
| US3950366A (en) * | 1973-05-10 | 1976-04-13 | Hercules Incorporated | Metal salts of 1,1,5,5-tetrasubstituted dithiobiurets |
| US4011318A (en) * | 1973-05-10 | 1977-03-08 | Hercules Incorporated | Metal salts of 1,1,5,5-tetrasubstituted dithiobiurets as population control agents |
| USRE29681E (en) * | 1973-05-10 | 1978-06-27 | Hercules Incorporated | Metal salts of 1,1,5,5-tetrasubstituted dithiobiurets |
| US3988438A (en) * | 1975-01-10 | 1976-10-26 | American Cyanamid Company | Hair conditioning shampoo |
| US4293713A (en) * | 1979-03-31 | 1981-10-06 | Taiho Pharmaceutical Company Limited | Novel 1,1,3,5-substituted biuret compound and a pharmaceutical composition containing the same |
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