US3703481A - Aqueous-based cosmetic detergent compositions - Google Patents
Aqueous-based cosmetic detergent compositions Download PDFInfo
- Publication number
- US3703481A US3703481A US109614A US3703481DA US3703481A US 3703481 A US3703481 A US 3703481A US 109614 A US109614 A US 109614A US 3703481D A US3703481D A US 3703481DA US 3703481 A US3703481 A US 3703481A
- Authority
- US
- United States
- Prior art keywords
- fatty acid
- monoester
- fatty
- compositions
- acid
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 239000000203 mixture Substances 0.000 title abstract description 52
- 239000003599 detergent Substances 0.000 title abstract description 27
- 239000002537 cosmetic Substances 0.000 title abstract description 15
- 239000000194 fatty acid Substances 0.000 abstract description 45
- 235000014113 dietary fatty acids Nutrition 0.000 abstract description 42
- 229930195729 fatty acid Natural products 0.000 abstract description 42
- 150000004665 fatty acids Chemical class 0.000 abstract description 37
- -1 ALKALI METAL SALT Chemical class 0.000 abstract description 19
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 abstract description 8
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 abstract description 6
- 229920006395 saturated elastomer Polymers 0.000 abstract description 6
- 229910052783 alkali metal Inorganic materials 0.000 abstract description 4
- 238000009736 wetting Methods 0.000 abstract description 4
- XLYOFNOQVPJJNP-PWCQTSIFSA-N Tritiated water Chemical compound [3H]O[3H] XLYOFNOQVPJJNP-PWCQTSIFSA-N 0.000 abstract 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 23
- 125000004432 carbon atom Chemical group C* 0.000 description 16
- 150000003839 salts Chemical class 0.000 description 16
- 239000004615 ingredient Substances 0.000 description 13
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 13
- 235000011044 succinic acid Nutrition 0.000 description 12
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 11
- 239000002453 shampoo Substances 0.000 description 11
- 239000001384 succinic acid Substances 0.000 description 11
- QZXSMBBFBXPQHI-UHFFFAOYSA-N N-(dodecanoyl)ethanolamine Chemical compound CCCCCCCCCCCC(=O)NCCO QZXSMBBFBXPQHI-UHFFFAOYSA-N 0.000 description 10
- 235000013162 Cocos nucifera Nutrition 0.000 description 9
- 244000060011 Cocos nucifera Species 0.000 description 9
- 125000000217 alkyl group Chemical group 0.000 description 8
- 239000004094 surface-active agent Substances 0.000 description 8
- 159000000000 sodium salts Chemical class 0.000 description 7
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 6
- 125000000129 anionic group Chemical group 0.000 description 6
- 239000000344 soap Substances 0.000 description 6
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical group C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 5
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 5
- 239000002253 acid Substances 0.000 description 5
- 125000001931 aliphatic group Chemical group 0.000 description 5
- 235000019441 ethanol Nutrition 0.000 description 5
- VBICKXHEKHSIBG-UHFFFAOYSA-N 1-monostearoylglycerol Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(O)CO VBICKXHEKHSIBG-UHFFFAOYSA-N 0.000 description 4
- 239000004166 Lanolin Substances 0.000 description 4
- 150000007513 acids Chemical class 0.000 description 4
- 125000002091 cationic group Chemical group 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 239000003974 emollient agent Substances 0.000 description 4
- 150000002148 esters Chemical class 0.000 description 4
- 150000002191 fatty alcohols Chemical class 0.000 description 4
- 235000011187 glycerol Nutrition 0.000 description 4
- 235000019388 lanolin Nutrition 0.000 description 4
- 229940039717 lanolin Drugs 0.000 description 4
- 239000002736 nonionic surfactant Substances 0.000 description 4
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid group Chemical group C(CCCCCCC\C=C/CCCCCCCC)(=O)O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 4
- 210000004761 scalp Anatomy 0.000 description 4
- 229910052708 sodium Inorganic materials 0.000 description 4
- 239000011734 sodium Substances 0.000 description 4
- ZZNDQCACFUJAKJ-UHFFFAOYSA-N 1-phenyltridecan-1-one Chemical compound CCCCCCCCCCCCC(=O)C1=CC=CC=C1 ZZNDQCACFUJAKJ-UHFFFAOYSA-N 0.000 description 3
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical class CCO LFQSCWFLJHTTHZ-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
- 239000003945 anionic surfactant Substances 0.000 description 3
- 239000003093 cationic surfactant Substances 0.000 description 3
- 238000004851 dishwashing Methods 0.000 description 3
- 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 3
- 238000001035 drying Methods 0.000 description 3
- 238000009472 formulation Methods 0.000 description 3
- 230000002209 hydrophobic effect Effects 0.000 description 3
- 239000006210 lotion Substances 0.000 description 3
- 231100000344 non-irritating Toxicity 0.000 description 3
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 3
- 229920000233 poly(alkylene oxides) Polymers 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- HXKKHQJGJAFBHI-UHFFFAOYSA-N 1-aminopropan-2-ol Chemical compound CC(O)CN HXKKHQJGJAFBHI-UHFFFAOYSA-N 0.000 description 2
- RTBFRGCFXZNCOE-UHFFFAOYSA-N 1-methylsulfonylpiperidin-4-one Chemical compound CS(=O)(=O)N1CCC(=O)CC1 RTBFRGCFXZNCOE-UHFFFAOYSA-N 0.000 description 2
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 2
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 2
- 229910019142 PO4 Inorganic materials 0.000 description 2
- KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 description 2
- DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 description 2
- 235000021355 Stearic acid Nutrition 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- 150000004996 alkyl benzenes Chemical class 0.000 description 2
- 150000003863 ammonium salts Chemical class 0.000 description 2
- JFCQEDHGNNZCLN-UHFFFAOYSA-N anhydrous glutaric acid Natural products OC(=O)CCCC(O)=O JFCQEDHGNNZCLN-UHFFFAOYSA-N 0.000 description 2
- 239000007859 condensation product Substances 0.000 description 2
- 230000003750 conditioning effect Effects 0.000 description 2
- 239000006071 cream Substances 0.000 description 2
- 150000001991 dicarboxylic acids Chemical class 0.000 description 2
- LVTYICIALWPMFW-UHFFFAOYSA-N diisopropanolamine Chemical compound CC(O)CNCC(C)O LVTYICIALWPMFW-UHFFFAOYSA-N 0.000 description 2
- 229940043276 diisopropanolamine Drugs 0.000 description 2
- 230000003292 diminished effect Effects 0.000 description 2
- 229940075507 glyceryl monostearate Drugs 0.000 description 2
- 239000008233 hard water Substances 0.000 description 2
- ACGUYXCXAPNIKK-UHFFFAOYSA-N hexachlorophene Chemical compound OC1=C(Cl)C=C(Cl)C(Cl)=C1CC1=C(O)C(Cl)=CC(Cl)=C1Cl ACGUYXCXAPNIKK-UHFFFAOYSA-N 0.000 description 2
- 229960004068 hexachlorophene Drugs 0.000 description 2
- 230000003165 hydrotropic effect Effects 0.000 description 2
- 230000000622 irritating effect Effects 0.000 description 2
- 229940102253 isopropanolamine Drugs 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 239000002932 luster Substances 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 239000001788 mono and diglycerides of fatty acids Substances 0.000 description 2
- 125000001421 myristyl 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])[H] 0.000 description 2
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 2
- 239000002304 perfume Substances 0.000 description 2
- 239000010452 phosphate Substances 0.000 description 2
- 229920000056 polyoxyethylene ether Polymers 0.000 description 2
- 150000003856 quaternary ammonium compounds Chemical class 0.000 description 2
- 239000002437 shaving preparation Substances 0.000 description 2
- 235000019333 sodium laurylsulphate Nutrition 0.000 description 2
- 239000003549 soybean oil Substances 0.000 description 2
- 235000012424 soybean oil Nutrition 0.000 description 2
- 239000008117 stearic acid Substances 0.000 description 2
- 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 2
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 2
- 239000003784 tall oil Substances 0.000 description 2
- XOAAWQZATWQOTB-UHFFFAOYSA-N taurine Chemical compound NCCS(O)(=O)=O XOAAWQZATWQOTB-UHFFFAOYSA-N 0.000 description 2
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 2
- HFVMEOPYDLEHBR-UHFFFAOYSA-N (2-fluorophenyl)-phenylmethanol Chemical compound C=1C=CC=C(F)C=1C(O)C1=CC=CC=C1 HFVMEOPYDLEHBR-UHFFFAOYSA-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
- DNIAPMSPPWPWGF-GSVOUGTGSA-N (R)-(-)-Propylene glycol Chemical class C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-N 0.000 description 1
- QLAJNZSPVITUCQ-UHFFFAOYSA-N 1,3,2-dioxathietane 2,2-dioxide Chemical compound O=S1(=O)OCO1 QLAJNZSPVITUCQ-UHFFFAOYSA-N 0.000 description 1
- LDVVTQMJQSCDMK-UHFFFAOYSA-N 1,3-dihydroxypropan-2-yl formate Chemical compound OCC(CO)OC=O LDVVTQMJQSCDMK-UHFFFAOYSA-N 0.000 description 1
- KQIXMZWXFFHRAQ-UHFFFAOYSA-N 1-(2-hydroxybutylamino)butan-2-ol Chemical compound CCC(O)CNCC(O)CC KQIXMZWXFFHRAQ-UHFFFAOYSA-N 0.000 description 1
- BTMZHHCFEOXAAN-UHFFFAOYSA-N 2-[bis(2-hydroxyethyl)amino]ethanol;2-dodecylbenzenesulfonic acid Chemical compound OCCN(CCO)CCO.CCCCCCCCCCCCC1=CC=CC=C1S(O)(=O)=O BTMZHHCFEOXAAN-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
- BCFOOQRXUXKJCL-UHFFFAOYSA-N 4-amino-4-oxo-2-sulfobutanoic acid Chemical class NC(=O)CC(C(O)=O)S(O)(=O)=O BCFOOQRXUXKJCL-UHFFFAOYSA-N 0.000 description 1
- BLFRQYKZFKYQLO-UHFFFAOYSA-N 4-aminobutan-1-ol Chemical compound NCCCCO BLFRQYKZFKYQLO-UHFFFAOYSA-N 0.000 description 1
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- ROSDSFDQCJNGOL-UHFFFAOYSA-N Dimethylamine Chemical class CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 description 1
- SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 1
- PZDIGVFNSSHZGD-UHFFFAOYSA-N FC(F)(Cl)Cl.FC(F)(Cl)CCl Chemical compound FC(F)(Cl)Cl.FC(F)(Cl)CCl PZDIGVFNSSHZGD-UHFFFAOYSA-N 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
- 239000004435 Oxo alcohol Substances 0.000 description 1
- 235000019482 Palm oil Nutrition 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical group CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 1
- 239000003568 Sodium, potassium and calcium salts of fatty acids Substances 0.000 description 1
- ULUAUXLGCMPNKK-UHFFFAOYSA-N Sulfobutanedioic acid Chemical class OC(=O)CC(C(O)=O)S(O)(=O)=O ULUAUXLGCMPNKK-UHFFFAOYSA-N 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical class OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 1
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical group C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 1
- 125000002252 acyl group Chemical group 0.000 description 1
- 239000001361 adipic acid Substances 0.000 description 1
- 235000011037 adipic acid Nutrition 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 239000000443 aerosol Substances 0.000 description 1
- 125000003158 alcohol group Chemical group 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 125000002877 alkyl aryl group Chemical group 0.000 description 1
- 150000008055 alkyl aryl sulfonates Chemical class 0.000 description 1
- 229940045714 alkyl sulfonate alkylating agent Drugs 0.000 description 1
- 150000008052 alkyl sulfonates Chemical class 0.000 description 1
- 125000002947 alkylene group Chemical group 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 150000001450 anions Chemical class 0.000 description 1
- 239000003242 anti bacterial agent Substances 0.000 description 1
- 229940077388 benzenesulfonate Drugs 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- WOWHHFRSBJGXCM-UHFFFAOYSA-M cetyltrimethylammonium chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCC[N+](C)(C)C WOWHHFRSBJGXCM-UHFFFAOYSA-M 0.000 description 1
- 239000003240 coconut oil Substances 0.000 description 1
- 235000019864 coconut oil Nutrition 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 235000012343 cottonseed oil Nutrition 0.000 description 1
- 239000002385 cottonseed oil Substances 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
- 230000007812 deficiency Effects 0.000 description 1
- 238000005238 degreasing Methods 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 1
- 229940043237 diethanolamine Drugs 0.000 description 1
- UKMSUNONTOPOIO-UHFFFAOYSA-N docosanoic acid Chemical compound CCCCCCCCCCCCCCCCCCCCCC(O)=O UKMSUNONTOPOIO-UHFFFAOYSA-N 0.000 description 1
- LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 description 1
- ILRSCQWREDREME-UHFFFAOYSA-N dodecanamide Chemical compound CCCCCCCCCCCC(N)=O ILRSCQWREDREME-UHFFFAOYSA-N 0.000 description 1
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical class CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 229940031098 ethanolamine Drugs 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 239000003676 hair preparation Substances 0.000 description 1
- 125000004356 hydroxy functional group Chemical group O* 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 125000000896 monocarboxylic acid group Chemical group 0.000 description 1
- 229910000403 monosodium phosphate Inorganic materials 0.000 description 1
- 235000019799 monosodium phosphate Nutrition 0.000 description 1
- WWZKQHOCKIZLMA-UHFFFAOYSA-N octanoic acid Chemical compound CCCCCCCC(O)=O WWZKQHOCKIZLMA-UHFFFAOYSA-N 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 235000019198 oils Nutrition 0.000 description 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
- 235000021313 oleic acid Nutrition 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 125000000962 organic group Chemical group 0.000 description 1
- 125000006353 oxyethylene group Chemical group 0.000 description 1
- 239000002540 palm oil Substances 0.000 description 1
- IPCSVZSSVZVIGE-UHFFFAOYSA-N palmitic acid group Chemical group C(CCCCCCCCCCCCCCC)(=O)O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 1
- 125000000913 palmityl 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])[H] 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 229920000223 polyglycerol Polymers 0.000 description 1
- 229940051841 polyoxyethylene ether Drugs 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 1
- 239000003352 sequestering agent Substances 0.000 description 1
- 239000008257 shaving cream Substances 0.000 description 1
- 239000002884 skin cream Substances 0.000 description 1
- AJPJDKMHJJGVTQ-UHFFFAOYSA-M sodium dihydrogen phosphate Chemical compound [Na+].OP(O)([O-])=O AJPJDKMHJJGVTQ-UHFFFAOYSA-M 0.000 description 1
- 239000001488 sodium phosphate Substances 0.000 description 1
- 235000013875 sodium salts of fatty acid Nutrition 0.000 description 1
- 229940048842 sodium xylenesulfonate Drugs 0.000 description 1
- QUCDWLYKDRVKMI-UHFFFAOYSA-M sodium;3,4-dimethylbenzenesulfonate Chemical compound [Na+].CC1=CC=C(S([O-])(=O)=O)C=C1C QUCDWLYKDRVKMI-UHFFFAOYSA-M 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-L succinate(2-) Chemical compound [O-]C(=O)CCC([O-])=O KDYFGRWQOYBRFD-UHFFFAOYSA-L 0.000 description 1
- 150000003444 succinic acids Chemical class 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- 229940124530 sulfonamide Drugs 0.000 description 1
- 150000003871 sulfonates Chemical class 0.000 description 1
- 230000000153 supplemental effect Effects 0.000 description 1
- 239000003760 tallow Substances 0.000 description 1
- 229960003080 taurine Drugs 0.000 description 1
- 229940105956 tea-dodecylbenzenesulfonate Drugs 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-O triethanolammonium Chemical compound OCC[NH+](CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-O 0.000 description 1
- 229960004418 trolamine Drugs 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 239000004711 α-olefin Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D10/00—Compositions of detergents, not provided for by one single preceding group
- C11D10/04—Compositions of detergents, not provided for by one single preceding group based on mixtures of surface-active non-soap compounds and soap
-
- 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
- A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
- A61K8/37—Esters of carboxylic acids
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q19/00—Preparations for care of the skin
- A61Q19/10—Washing or bathing preparations
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/88—Ampholytes; Electroneutral compounds
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/02—Anionic compounds
- C11D1/12—Sulfonic acids or sulfuric acid esters; Salts thereof
- C11D1/14—Sulfonic acids or sulfuric acid esters; Salts thereof derived from aliphatic hydrocarbons or mono-alcohols
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/02—Anionic compounds
- C11D1/12—Sulfonic acids or sulfuric acid esters; Salts thereof
- C11D1/18—Sulfonic acids or sulfuric acid esters; Salts thereof derived from amino alcohols
- C11D1/20—Fatty acid condensates
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/02—Anionic compounds
- C11D1/12—Sulfonic acids or sulfuric acid esters; Salts thereof
- C11D1/29—Sulfates of polyoxyalkylene ethers
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/38—Cationic compounds
- C11D1/52—Carboxylic amides, alkylolamides or imides or their condensation products with alkylene oxides
- C11D1/523—Carboxylic alkylolamides, or dialkylolamides, or hydroxycarboxylic amides (R1-CO-NR2R3), where R1, R2 or R3 contain one hydroxy group per alkyl group
-
- 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
- Surfactant compositions including cosmetic surfactant compositions such as shampoos, shaving creams, skin cleansing compositions and the like, containing various derivatives of polycarboxylic acids are known to the art and are disclosed, for example, in US. Pats. No. 2,452,- 043, issued Oct. 26, 1948 to Lawrence H. Flett; No. 2,490,459, issued Dec. 6, 1949 to Werner Max Lilienfeld; -No. 2,562,154, issued July 24, 1951 to Emil A. Vitalis; and 2,878,190, issued Mar. 17, 1959 to Vladimir Dvorkovitz et al.
- Compounds therein disclosed include, among others, succinic acids, sulfosuccinic acids, sulfosuccinamic acids, esters, sulfosuccinic esters of fatty alkanolamides and salts thereof and various derivatives thereof, and are reported as useful in surfactant compositions, particularly shampoos.
- the aforesaid have numerous deficiencies preventing their use in a wide variety of aqueous-based surfactant compositions as opposed to the fatty alkanolamide monoester salt additives more particularly described herein.
- aqueous based cosmetic detergent compositions comprising water, a member of the group of synthetic anionic, nonionic and cationic organic detergents and compatible mixtures of same, and from about 1 to 20%, preferably 3 to by weight, of a member of the group of ammonium, C -C alkanolamine and alkali metal salts of the monoester of a C -C saturated, unsubstituted, aliphatic dicarboxylic acid with fatty acid monoand dialkanol-amides wherein the alkanol portion contains up to 8 carbon atoms.
- compositions of the present invention contain, as an essential ingredient, from about 1 to 20%, by weight, of an aforesaid salt of a monoester of a C -C saturated, aliphtic dicarboxylic acid such as succinic, malonic, glutaric or adipic acid with a fatty acid alkanolamide.
- an aforesaid salt of a monoester of a C -C saturated, aliphtic dicarboxylic acid such as succinic, malonic, glutaric or adipic acid with a fatty acid alkanolamide.
- the fatty acid alkanolamides are well known to the art and generally comprise those prepared from saturated and unsaturated aliphatic monocarboxylic acids containing from about 8 to 22 carbon atoms and preferably those containing from about 10 to 18 carbon atoms.
- Exemplary fatty acids are caprylic, capric, lauric, myristic, palmitic, stearic, arachidic, behenic, oleic, linoleic and eleostearic acids and the like, as well as mixed fatty acids such as tall oil fatty acids, hydrogenated tallow fatty acids, coconut oil fatty acids and vegetable fatty acids such as are derived from cottonseed and soybean oil, as well as rosin fatty acids.
- the alkanolamines which may be condensed with the aforesaid fatty acids comprise both monoand dialkanolamines containing up to 8 carbon atoms and are exemplified by monoethanolamine, diethanolamide, isopropanolamine, diisopropanolamine, butanolamine, dibutanolamine, diisobutanolamine and the like.
- fatty acid alkanolamides may be prepared by various well known techniques such as by condensing equimolar quantities of fatty acid with alkanolamine, or by condensing a molar excess of alkanolamine with fatty acid or by reacting a fatty acid ester with alkanolamine, or by oxyalkylating, such as oxyethylating, the amide of the fatty acid.
- Particularly preferred fatty alkanolamides are fatty acid monoalkanolamides, particularly monoethanolamides.
- the monoesters are prepared, for instance, by reacting appropriate substantially stoichiometric quantities of C -C aliphatic saturated dicarboxylic acids with the aforesaid fatty acid alkanolamides in order to prepare fatty acid alkanolamidedicarboxylic acid monoesters having one free COOH available for salt formation.
- the fatty acid alkanolamide is preferably esterified with succinic acid.
- the monoester salts may be the water-soluble ammonium, C -C alkanolamine such as ethanolamine, diethanolamine, triethanolamine, isopropanolamine, diisopropanolamine and the like, or alkali metal salts, of the aforesaid monoesters of the fatty acid alkanolamides with dicarboxylic acids.
- the monoester salt will be the sodium salt.
- the aforesaid salts of fatty acid alkanolamide-dicarboxylic acid monoesters are employable in a wide variety of aqueous-based cosmetic detergent compositions.
- These cosmetic detergent compositions will generally contain, in addition to the aforesaid salt of a fatty acid alkanolamide-dicarboxylic acid monoester present in amounts varying between 1 and 20%, preferably 3 to 10%, by weight, a quantity of water in the range of about 10 to by weight, and the balance will be a member of the group of synthetic organic detergents of the anionic, nonionic or cationic type.
- compositions of the present invention encompass shampoos, hair preparations such as conditioners and rinses, shaving preparations, especially aerosol shave preparation, skin conditioners and cleansing compositions, dishwashing detergent compositions, hand lotions, bubblebath compositions and the like.
- the synthetic organic detergents or surface-active agents which may be employed in the compositions of the present invention may be selected from a wide variety of water-soluble anionic, nonionic or cationic surfactants such as are generally employed in aqueous cosmetic detergent or surfactant compositions which are meant to come into contact with the skin or hair.
- Exemplary anionic materials are the water-soluble, straight and branched chain alkyl aryl sulfonates, particularly the alkyl benzene sulfonates, wherein the alkyl group contains from about 8 to 15 carbon atoms, the lower alkyl aryl or hydrotropic sulfonates such as sodium xylene sulfonate; the olefin sulfonates such as those produced by sulfonating a C to C straight chain alphaolefin; hydroxy C to C alkyl sulfonates; water-soluble alkene disulfonates containing from about 10 to 24 carbon atoms; the normal and secondary higher alkyl detergents, particularly those having about 8 to 15 carbon atoms in the alcohol residue such as lauryl or coconut fatty alcohol sulfate; sulfuric acid esters of polyhydric alcohols partially esterified With higher fatty acids such as coconut oil monoglyceride monosulfate, coconut ethanolamide sul
- Exemplary nonionic detergents which may be employed in the compositions of the present invention are the polyalkylene oxide condensation products with a hydrophobic organic compound.
- the hydrophobic organic group usually contains from about 8 to 30 carbon atoms and is condensed with from about to 50 alkylene oxide groups such as ethylene oxide, propylene oxide, butylene oxide, and the like.
- Specific condensation products include the polyoxyethylene ethers of alkyl phenols wherein the alkyl group contains from about 6 to 12 carbon atoms and containing from about 8 to 18 mols of ethylene oxide per mol of said alkyl phenols; polyalkylene oxide ethers of fatty alcohols such as lauryl, myristyl, cetyl, stearyl and oleyl alcohols, and C to C oxo alcohols, which are condensed with from about 10 to 30 mols of ethylene oxide per mol of said alcohols; polyoxyalkylene esters of organic acids such as the higher fatty acids, rosin acids, tall oil acids and the like, said esters containing from about 12 to 30 mols of ethylene oxide and about 8 to 22 carbon atoms in the acyl group; polyalkylene oxides condensates with higher fatty acid amides, such as the higher fatty acid primary amides, monoand diethanolamides as well as condensates of higher fatty acid s
- nonionic surfactants are the higher fatty acid alkanolamides, such as the monoethanolamides, diethanolamides and isopropanolamides wherein the acyl radical has an average of from about 10 to 18 carbon atoms.
- examples are coconut fatty acid, capric, lauric, oleic and myristic diethanolamides and the correspondnig monoethanolamides and isopropanolamides; the fatty tertiary amine oxides which may be represented by the general formula R R R N O wherein R represents C to C alkyl such as decyl, dodecyl, tetradecyl, octadecyl and the like and R and R represent methyl or ethyl.
- Particularly preferred members of the above group of nonionic surfactants include the fatty acid alkanolamides and the polyoxyalkylene, particularly the ethylene oxide condensates thereof.
- Exemplary cationic surfactants which may be employed in the compositions of the present invention are quaternary ammonium salts having long chain hydrophobic radicals such as C to C alkyl radicals as exemplified by l-methyl-l-higher alkyl amido-ethyl-Z-higher alkyl imidazolinum salts wherein the alkyl groups have 10 to 20 carbon atoms, ethoxylated long chain fatty quaternary ammonium compounds, higher alkyl benzyldimethylammonium salts, higher alkyl isoquinolinium salts, di (higher alkyl) dimethylammonium salts, and the like.
- the anion of the water-soluble quaternary ammonium compound is most usually a chloride or methosulfate, but other ions may be used such as bromide, phosphate, dialkyl phosphate or acetate ions.
- anionic, cationic and nonionic surfactants are generally present in amounts ranging from about 5 to 85%, by weight, depending upon the particular cosmetic formulation prepared. Admixtures of the aforesaid may be employed so long as such admixtures are compatible and do not cause precipitation or otherwise adversely affect the stability of the system.
- Exemplary cosmetic detergent compositions are shampoos containing water, 5-10% fatty amine oxide, 3-5% sodium fatty alcohol sulfate and about 3-5% of said C C dicarboxylic acid-fatty acid alkanolamide monoester salt; dishwashing liquids containing 1520% alkyl benzene sulfonate, 510% sulfated ethoxylated aliphatic alcohol, 310% hydrotropic sulfonate and from 5-10% of said C -C aliphatic dicarboxylic acid-fatty acid alkanolamide monoester salt; shampoo bars containing 60-70% mixed fatty acid soaps and 10-20% of said C -C aliphatic dicarboxylic acid-fatty acid alkanolamide monoester and the like.
- compositions of the present invention such as are generally employed in cosmetic preparations.
- additives such as lanolin, ethoxylated lanolin, glycerol and polyglycerols, lower alcohols such as ethanols, dyes, perfumes, antibacterial agents such as hexachlorophene, preservative agents such as formalin, sequestering agents such as water-soluble phosphate compounds and the like.
- aqueous-based cosmetic detergent compositions of the present invention possess a number of highly significant advantages. They exhibit excellent emolliency when applied to the skin as hand lotions, skin cleansing compositions, shaving creams, or in the form of dishwashing detergents. Emolliency refers to the desirable after-feel imparted to the skin and the conditioning and protective effects on the skin by the retention of natural greases or oils and the prevention and relief of dryness.
- Shampoos formulated in accordance with the present invention impart an observable improved manageability and luster t0 the hair and emolliency to the scalp, and in addition, they have a diminished degreasing effect and are non-irritating to the scalp and skin.
- compositions such as shaving preparations also show excellent wetting and lathering properties and produce a soothing and non-irritating effect upon the skin.
- compositions of the present invention have the capacity to reduce and suppress the irritating tendency of conventional detergents commonly employed in detergent compositions. Even in hard water, wetting and lathering properties are not substantially diminished.
- a shampoo is prepared containing the following ingredients:
- EXAMPLE II (d) Ethanol 10 (e) Ammonium salt of the monoester of lauric monoet-hanolamide and succinic acid 5 (f) Water 54
- the above formulation is found not only to be nonirritating to the skin but produces an emollient effect on the skin after use.
- the identical composition, except for the ammonium lauric monoethanolamide monosuccinate is prepared for purposes of comparison and is found to produce a pronounced drying effect on the hands with little or no emollient effect on the skin perceptible.
- This soap bar forms a lather with water which is quite copious, similar to that of a shampoo lather and has a desirable after-feel on the skin.
- EMMPLE IV A shampoo is prepared by combining the following ingredients:
- EXAMPLE VI A various emollient hand lotion is prepared by combining the following ingredients:
- a composition suitable as a skin-cleansing liquid or bubble-bath composition is prepared employing the following components:
- a shampoo is prepared by combining the following ingredients:
- a hairdressing composition is prepared by combining the following ingredients:
- a shaving cream suitable for use in aerosol-type dispensers is prepared by combining the following ingredients:
- EXAMPLE XI An emollient skin cream is prepared by combining the following ingredients:
- An aqueous-based cosmetic detergent composition which consists essentially of (a) from about 10% to 90%, by weight, of water; (b) from about 1% to 20%, by Weight, of a member of the group consisting of ammonium, C -C alkanolamine and alkali metal salts of monoesters of C -C saturated, unsubstituted, aliphatic dicarboxylic acids with fatty acid monoand di-alkanolamides wherein the alkanol portion contains up to 8 carbon atoms; and (c) from 5% to by weight, of a member of the group consisting of synthetic anionic, nonionic and cationic organic detergents and compatible mixtures of same with the proviso that said (0) ingredient is distinct from said (b) ingredient.
- composition according to claim 1 wherein said aliphatic dicarboxylic acid is succinic acid.
- composition according to claim 1 wherein said fatty acid contains from 10 to 18 carbon atoms.
- composition according to claim 1 wherein said salt is a sodium salt.
- composition according to claim 1 wherein said synthetic organic detergent is a fatty alcohol sulfate.
- composition according to claim 1 wherein said synthetic organic detergent is a member of the group consisting of fatty acid salts, fatty acid soaps and mixtures thereof.
- composition according to claim 1 wherein said synthetic organic detergent is a fatty acid alkanolamide.
- a composition according to claim 6 wherein said monoester salt is the sodium salt of the monoester of succinic acid and coconut monoethanolamide.
- monoester salt is the triethanolamine salt of the monoester of succinic acid and lauric monoethanolamide.
- composition according to claim 6 wherein said 15 424-47 73
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Abstract
IMPROVED AQUEOUS DETERGENT COMPOSITIONS FOR COSMETIC APPLICATIONS COMPRISING WATER, A SYNTHETIC ORGANIC DETERGENT, AND FROM ABOUT 1-20%, BY WEIGHT, OR AN AMMONIUM, ALKANOLAMINE OR ALKALI METAL SALT OF A MONOESTER OF A C3-C6 SATURATED ALIPHATIC DICARBOXYLIC ACID WITH A FATTY ACID ALKANOLAMIDE. THE COMPOSITONS EXHIBIT IMPROVED PROPERTIES WITH REGARD TO EMOLLIENCY, WETTING LATHERING AND THE LIKE.
Description
United States Patent Ofice 3,703,481 Patented Nov. 21, 1972 3,703,481 AQUEOUS-BASED COSMETIC DETERGENT COMPOSITIONS Graham Barker, Fair Lawn, N.J., and Herman W. Campbell, Chicago, Ill., assignors to Witco Chemical Corporation, New York, N.Y. No Drawing. Filed- Jan. 25, 1971, Ser. No. 109,614 Int. Cl. Clld 1/20 US. Cl. 252546 11 Claims ABSTRACT OF THE DISCLOSURE This invention relates to improved detergent and surfactant compositions. More particularly, this invention relates to improved aqueous-based cosmetic detergent compositions having improved characteristics with regard to emolliency, wetting, lathering, hair manageability, counter-irritancy and the like.
Surfactant compositions, including cosmetic surfactant compositions such as shampoos, shaving creams, skin cleansing compositions and the like, containing various derivatives of polycarboxylic acids are known to the art and are disclosed, for example, in US. Pats. No. 2,452,- 043, issued Oct. 26, 1948 to Lawrence H. Flett; No. 2,490,459, issued Dec. 6, 1949 to Werner Max Lilienfeld; -No. 2,562,154, issued July 24, 1951 to Emil A. Vitalis; and 2,878,190, issued Mar. 17, 1959 to Vladimir Dvorkovitz et al. Compounds therein disclosed include, among others, succinic acids, sulfosuccinic acids, sulfosuccinamic acids, esters, sulfosuccinic esters of fatty alkanolamides and salts thereof and various derivatives thereof, and are reported as useful in surfactant compositions, particularly shampoos. However, the aforesaid have numerous deficiencies preventing their use in a wide variety of aqueous-based surfactant compositions as opposed to the fatty alkanolamide monoester salt additives more particularly described herein.
In accordance with the present invention, there have been discovered improved aqueous based cosmetic detergent compositions comprising water, a member of the group of synthetic anionic, nonionic and cationic organic detergents and compatible mixtures of same, and from about 1 to 20%, preferably 3 to by weight, of a member of the group of ammonium, C -C alkanolamine and alkali metal salts of the monoester of a C -C saturated, unsubstituted, aliphatic dicarboxylic acid with fatty acid monoand dialkanol-amides wherein the alkanol portion contains up to 8 carbon atoms.
The compositions of the present invention contain, as an essential ingredient, from about 1 to 20%, by weight, of an aforesaid salt of a monoester of a C -C saturated, aliphtic dicarboxylic acid such as succinic, malonic, glutaric or adipic acid with a fatty acid alkanolamide.
The fatty acid alkanolamides are well known to the art and generally comprise those prepared from saturated and unsaturated aliphatic monocarboxylic acids containing from about 8 to 22 carbon atoms and preferably those containing from about 10 to 18 carbon atoms. Exemplary fatty acids are caprylic, capric, lauric, myristic, palmitic, stearic, arachidic, behenic, oleic, linoleic and eleostearic acids and the like, as well as mixed fatty acids such as tall oil fatty acids, hydrogenated tallow fatty acids, coconut oil fatty acids and vegetable fatty acids such as are derived from cottonseed and soybean oil, as well as rosin fatty acids. The alkanolamines which may be condensed with the aforesaid fatty acids comprise both monoand dialkanolamines containing up to 8 carbon atoms and are exemplified by monoethanolamine, diethanolamide, isopropanolamine, diisopropanolamine, butanolamine, dibutanolamine, diisobutanolamine and the like. These fatty acid alkanolamides may be prepared by various well known techniques such as by condensing equimolar quantities of fatty acid with alkanolamine, or by condensing a molar excess of alkanolamine with fatty acid or by reacting a fatty acid ester with alkanolamine, or by oxyalkylating, such as oxyethylating, the amide of the fatty acid. Particularly preferred fatty alkanolamides are fatty acid monoalkanolamides, particularly monoethanolamides.
The monoesters are prepared, for instance, by reacting appropriate substantially stoichiometric quantities of C -C aliphatic saturated dicarboxylic acids with the aforesaid fatty acid alkanolamides in order to prepare fatty acid alkanolamidedicarboxylic acid monoesters having one free COOH available for salt formation. The fatty acid alkanolamide is preferably esterified with succinic acid. The monoester salts may be the water-soluble ammonium, C -C alkanolamine such as ethanolamine, diethanolamine, triethanolamine, isopropanolamine, diisopropanolamine and the like, or alkali metal salts, of the aforesaid monoesters of the fatty acid alkanolamides with dicarboxylic acids. Preferably the monoester salt will be the sodium salt.
The aforesaid salts of fatty acid alkanolamide-dicarboxylic acid monoesters are employable in a wide variety of aqueous-based cosmetic detergent compositions. These cosmetic detergent compositions will generally contain, in addition to the aforesaid salt of a fatty acid alkanolamide-dicarboxylic acid monoester present in amounts varying between 1 and 20%, preferably 3 to 10%, by weight, a quantity of water in the range of about 10 to by weight, and the balance will be a member of the group of synthetic organic detergents of the anionic, nonionic or cationic type.
The particular synthetic organic detergent, surfactant, soap or mixture thereof chosen for employment in the compositions of the prevent invention will be dependent upon the particular cosmetic preparation sought to be prepared. The compositions of the present invention encompass shampoos, hair preparations such as conditioners and rinses, shaving preparations, especially aerosol shave preparation, skin conditioners and cleansing compositions, dishwashing detergent compositions, hand lotions, bubblebath compositions and the like.
The synthetic organic detergents or surface-active agents which may be employed in the compositions of the present invention may be selected from a wide variety of water-soluble anionic, nonionic or cationic surfactants such as are generally employed in aqueous cosmetic detergent or surfactant compositions which are meant to come into contact with the skin or hair.
Exemplary anionic materials are the water-soluble, straight and branched chain alkyl aryl sulfonates, particularly the alkyl benzene sulfonates, wherein the alkyl group contains from about 8 to 15 carbon atoms, the lower alkyl aryl or hydrotropic sulfonates such as sodium xylene sulfonate; the olefin sulfonates such as those produced by sulfonating a C to C straight chain alphaolefin; hydroxy C to C alkyl sulfonates; water-soluble alkene disulfonates containing from about 10 to 24 carbon atoms; the normal and secondary higher alkyl detergents, particularly those having about 8 to 15 carbon atoms in the alcohol residue such as lauryl or coconut fatty alcohol sulfate; sulfuric acid esters of polyhydric alcohols partially esterified With higher fatty acids such as coconut oil monoglyceride monosulfate, coconut ethanolamide sulfate, lauric acid amide or taurine and the like; the various soaps or salts of fatty acids containing from about 8 to 22, particularly 10 to 18, carbon atoms, such as the sodium, potassium, ammonium and lower alkanolamine, particularly mono-, diand triethanolamine salts of fatty acids such as stearic acid, oleic acid, coconut fatty acid, fatty acids derived from palm oil, soybean oil, tallow and the like. Particularly preferred anionic surfactants include the fatty alcohol and ether alcohol sulfates and the sodium salts of fatty acids containing from about 12 to 18 carbon atoms.
Exemplary nonionic detergents which may be employed in the compositions of the present invention are the polyalkylene oxide condensation products with a hydrophobic organic compound. The hydrophobic organic group usually contains from about 8 to 30 carbon atoms and is condensed with from about to 50 alkylene oxide groups such as ethylene oxide, propylene oxide, butylene oxide, and the like. Specific condensation products include the polyoxyethylene ethers of alkyl phenols wherein the alkyl group contains from about 6 to 12 carbon atoms and containing from about 8 to 18 mols of ethylene oxide per mol of said alkyl phenols; polyalkylene oxide ethers of fatty alcohols such as lauryl, myristyl, cetyl, stearyl and oleyl alcohols, and C to C oxo alcohols, which are condensed with from about 10 to 30 mols of ethylene oxide per mol of said alcohols; polyoxyalkylene esters of organic acids such as the higher fatty acids, rosin acids, tall oil acids and the like, said esters containing from about 12 to 30 mols of ethylene oxide and about 8 to 22 carbon atoms in the acyl group; polyalkylene oxides condensates with higher fatty acid amides, such as the higher fatty acid primary amides, monoand diethanolamides as well as condensates of higher fatty acid sulfonamides.
Further suitable nonionic surfactants are the higher fatty acid alkanolamides, such as the monoethanolamides, diethanolamides and isopropanolamides wherein the acyl radical has an average of from about 10 to 18 carbon atoms. Examples are coconut fatty acid, capric, lauric, oleic and myristic diethanolamides and the correspondnig monoethanolamides and isopropanolamides; the fatty tertiary amine oxides which may be represented by the general formula R R R N O wherein R represents C to C alkyl such as decyl, dodecyl, tetradecyl, octadecyl and the like and R and R represent methyl or ethyl.
Particularly preferred members of the above group of nonionic surfactants include the fatty acid alkanolamides and the polyoxyalkylene, particularly the ethylene oxide condensates thereof.
Exemplary cationic surfactants which may be employed in the compositions of the present invention are quaternary ammonium salts having long chain hydrophobic radicals such as C to C alkyl radicals as exemplified by l-methyl-l-higher alkyl amido-ethyl-Z-higher alkyl imidazolinum salts wherein the alkyl groups have 10 to 20 carbon atoms, ethoxylated long chain fatty quaternary ammonium compounds, higher alkyl benzyldimethylammonium salts, higher alkyl isoquinolinium salts, di (higher alkyl) dimethylammonium salts, and the like. The anion of the water-soluble quaternary ammonium compound is most usually a chloride or methosulfate, but other ions may be used such as bromide, phosphate, dialkyl phosphate or acetate ions.
The aforesaid anionic, cationic and nonionic surfactants are generally present in amounts ranging from about 5 to 85%, by weight, depending upon the particular cosmetic formulation prepared. Admixtures of the aforesaid may be employed so long as such admixtures are compatible and do not cause precipitation or otherwise adversely affect the stability of the system.
Exemplary cosmetic detergent compositions are shampoos containing water, 5-10% fatty amine oxide, 3-5% sodium fatty alcohol sulfate and about 3-5% of said C C dicarboxylic acid-fatty acid alkanolamide monoester salt; dishwashing liquids containing 1520% alkyl benzene sulfonate, 510% sulfated ethoxylated aliphatic alcohol, 310% hydrotropic sulfonate and from 5-10% of said C -C aliphatic dicarboxylic acid-fatty acid alkanolamide monoester salt; shampoo bars containing 60-70% mixed fatty acid soaps and 10-20% of said C -C aliphatic dicarboxylic acid-fatty acid alkanolamide monoester and the like.
Various supplemental materials may be added to the compositions of the present invention such as are generally employed in cosmetic preparations. Exemplary are additives such as lanolin, ethoxylated lanolin, glycerol and polyglycerols, lower alcohols such as ethanols, dyes, perfumes, antibacterial agents such as hexachlorophene, preservative agents such as formalin, sequestering agents such as water-soluble phosphate compounds and the like.
The aqueous-based cosmetic detergent compositions of the present invention possess a number of highly significant advantages. They exhibit excellent emolliency when applied to the skin as hand lotions, skin cleansing compositions, shaving creams, or in the form of dishwashing detergents. Emolliency refers to the desirable after-feel imparted to the skin and the conditioning and protective effects on the skin by the retention of natural greases or oils and the prevention and relief of dryness. Shampoos formulated in accordance with the present invention impart an observable improved manageability and luster t0 the hair and emolliency to the scalp, and in addition, they have a diminished degreasing effect and are non-irritating to the scalp and skin. Moreover, compositions such as shaving preparations also show excellent wetting and lathering properties and produce a soothing and non-irritating effect upon the skin. Generally the compositions of the present invention have the capacity to reduce and suppress the irritating tendency of conventional detergents commonly employed in detergent compositions. Even in hard water, wetting and lathering properties are not substantially diminished.
The invention is further illustrated by the following examples, which are not to be considered as limitative of its scope. Percentages are by weight.
EXAMPLE I A shampoo is prepared containing the following ingredients:
Percent (a) Sodium lauryl sulfate 7 (b) Lauric diethanolamide 3 (c) Triethanolamine salt of the monoester of succinic acid and coconut monoethanolamide 3 (d) Water 87 The above formulation is found to be high lathering even in hard water, and non-drying to the hair and scalp. It is observed that after use, the hair has good manageability and luster, and does not require the use of a hair conditioning rinse.
EXAMPLE II (d) Ethanol 10 (e) Ammonium salt of the monoester of lauric monoet-hanolamide and succinic acid 5 (f) Water 54 The above formulation is found not only to be nonirritating to the skin but produces an emollient effect on the skin after use. The identical composition, except for the ammonium lauric monoethanolamide monosuccinate is prepared for purposes of comparison and is found to produce a pronounced drying effect on the hands with little or no emollient effect on the skin perceptible.
EXAMPLE 'III A soap bar is prepared by combining the following ingredients:
This soap bar forms a lather with water which is quite copious, similar to that of a shampoo lather and has a desirable after-feel on the skin.
EMMPLE IV A shampoo is prepared by combining the following ingredients:
Percent (a) Coconut diethanolamide 5.0 (b) Sodium lauryl sulfate 9.0
(c) Triethanolamine dodecyl benzene sulfonate 8.0
(d) Perfume 0.4 (e) Monosodium phosphate 0.6 (f) Sodium salt of the monoester of malonic acid with oleic isopropanolamide 2.0 (g) Water 75 The product when applied to the hair significantly improves manageability with no drying eifect on the scalp.
EXAM'PLE V Example IV is repeated, except that for ingredient (f) there is employed the ammonium salt of the monoester of glutaric acid with lauric diethanolamide and equivalent results are obtained.
EXAMPLE VI A various emollient hand lotion is prepared by combining the following ingredients:
Percent (a) Lanolin 2.0 (b) Coconut diethanolamide 20.0 Sodium salt of the monoester of succinic acid with coconut butanolamide 5 .0 (d) Hexachlorop-hene 1.0 (e) Water 72 EXAMPLE VII A composition suitable as a skin-cleansing liquid or bubble-bath composition is prepared employing the following components:
A shampoo is prepared by combining the following ingredients:
Percent (a) Triethanolammonium coconut sulfate 8.0
(b) Sodium alkyl (C -C sulfate 7.0
(c) Sodium t-octylphenl sulfonate 6.0 ((1) Potassium salt of the monoester of succinic acid and lauric monoethanolamide 1.0
(e) Water 78 6 EXAMPLE IX A hairdressing composition is prepared by combining the following ingredients:
Percent (a) Polyoxyethylene ether of lauryl alcohol having 23 oxyethylene units 5.0 (b) Lauric diethanolamide 6.0 (c) Lanolin 2.0 (d) Sodium salt of the monoester of succinic acid and coconut monoethanolamide 5.0 (e) Glycerine 10.0 (f) Water 72 EXAMPLE X A shaving cream suitable for use in aerosol-type dispensers is prepared by combining the following ingredients:
Percent (a) Glycerol 10.0 (b) Triethanolamine 4.0 (c) Stearic acid 4.5 (d) Coconut fatty acids 1.5 (e) Glyceryl monostearate 5.0
(f) Triethanolamine salt of coconut monoethanolamide succinic acid monoester 3.0 (g) Water 66.0 (h) Propellent (dichlorodifluoromethane-dichlorodifluoroethane mixture) 6.0
EXAMPLE XI An emollient skin cream is prepared by combining the following ingredients:
Percent (a) Glyceryl monostearate 10.0 (b) Glycerol 15.0 (c) Cetyl trimethyl ammonium chloride 0.2
(d) Sodium salt of the monoester of succinic acid and coconut monoethanolamide (e) Water 69.8
EXAMPLE XII A shampoo is prepared by combining the following ingredients and is observed by the user to impart a greater What is claimed is:
1. An aqueous-based cosmetic detergent composition which consists essentially of (a) from about 10% to 90%, by weight, of water; (b) from about 1% to 20%, by Weight, of a member of the group consisting of ammonium, C -C alkanolamine and alkali metal salts of monoesters of C -C saturated, unsubstituted, aliphatic dicarboxylic acids with fatty acid monoand di-alkanolamides wherein the alkanol portion contains up to 8 carbon atoms; and (c) from 5% to by weight, of a member of the group consisting of synthetic anionic, nonionic and cationic organic detergents and compatible mixtures of same with the proviso that said (0) ingredient is distinct from said (b) ingredient.
2. A composition according to claim 1 wherein said aliphatic dicarboxylic acid is succinic acid.
3. A compostion according to claim 1 wherein said fatty acid alkanolamide is a monoalkanolamide.
4. A composition according to claim 1 wherein said fatty acid contains from 10 to 18 carbon atoms.
5. A composition according to claim 1 wherein said salt is a sodium salt.
6. A composition according to claim 1 wherein said salts of said monoesters are present in an amount of from about 3% to about 10% by weight.
7. A composition according to claim 1 wherein said synthetic organic detergent is a fatty alcohol sulfate.
8. A composition according to claim 1 wherein said synthetic organic detergent is a member of the group consisting of fatty acid salts, fatty acid soaps and mixtures thereof.
9. A composition according to claim 1 wherein said synthetic organic detergent is a fatty acid alkanolamide.
10. A composition according to claim 6 wherein said monoester salt is the sodium salt of the monoester of succinic acid and coconut monoethanolamide.
monoester salt is the triethanolamine salt of the monoester of succinic acid and lauric monoethanolamide.
References Cited UNITED STATES PATENTS 2,173,448 9/1939 Katzman et al. 260404 2,733,212 1/ 1956 Epstein et a] 252-117 2,343,431 3/ 1944 Wells et a1 260-404 X 10 RICHARD D. LOVERING, Primary Examiner U.S. Cl. X.R.
252-90, 117, 134, 356, 527, 548, DIG. 5, DIG. 13;
11. A composition according to claim 6 wherein said 15 424-47 73
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US10961471A | 1971-01-25 | 1971-01-25 |
Publications (1)
Publication Number | Publication Date |
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US3703481A true US3703481A (en) | 1972-11-21 |
Family
ID=22328619
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US109614A Expired - Lifetime US3703481A (en) | 1971-01-25 | 1971-01-25 | Aqueous-based cosmetic detergent compositions |
Country Status (2)
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US (1) | US3703481A (en) |
CA (1) | CA938557A (en) |
Cited By (23)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3996148A (en) * | 1974-07-25 | 1976-12-07 | Pierre Fusey | Basic detergent for liquid lyes |
US4101293A (en) * | 1977-03-30 | 1978-07-18 | Reichhold Chemicals, Inc. | Stabilizing emulsifiers |
FR2432309A1 (en) * | 1978-07-31 | 1980-02-29 | Kao Corp | COMPOSITION FOR RINSING HAIR BASED ON A SUCCINIC ACID DERIVATIVE AND A QUATERNARY AMMONIUM SALT |
US4304573A (en) * | 1980-01-22 | 1981-12-08 | Gulf & Western Industries, Inc. | Process of beneficiating coal and product |
US4306997A (en) * | 1976-01-16 | 1981-12-22 | Lever Brothers Company | Foam bath compositions containing anionic detergent and monoglyceride |
US4358293A (en) * | 1981-01-29 | 1982-11-09 | Gulf & Western Manufacturing Co. | Coal-aqueous mixtures |
US4406664A (en) * | 1980-01-22 | 1983-09-27 | Gulf & Western Industries, Inc. | Process for the enhanced separation of impurities from coal and coal products produced therefrom |
US4430245A (en) | 1981-04-06 | 1984-02-07 | Internationale Octrooi Maatschappij "Octropa" B.V. | Soap composition |
US4462981A (en) * | 1982-12-10 | 1984-07-31 | Creative Products Resource, Associates Ltd. | Cosmetic applicator useful for skin moisturizing and deodorizing |
US4526585A (en) * | 1981-05-28 | 1985-07-02 | The Standard Oil Company | Beneficiated coal, coal mixtures and processes for the production thereof |
US4536372A (en) * | 1980-01-22 | 1985-08-20 | The Standard Oil Company | Apparatus for beneficiating coal |
US4550035A (en) * | 1982-12-10 | 1985-10-29 | Creative Products Resource Associates, Ltd. | Cosmetic applicator useful for skin moisturizing and deodorizing |
US4583990A (en) * | 1981-01-29 | 1986-04-22 | The Standard Oil Company | Method for the beneficiation of low rank coal |
US4673525A (en) * | 1985-05-13 | 1987-06-16 | The Procter & Gamble Company | Ultra mild skin cleansing composition |
EP0259843A2 (en) * | 1986-09-09 | 1988-03-16 | S.C. Johnson & Son, Inc. | Post-foaming gel with an unsaturated or non-linear dialkanolamide or a monoalkanolamide |
US4812253A (en) * | 1985-05-13 | 1989-03-14 | The Procter & Gamble Company | Ultra mild skin cleansing composition |
US4863628A (en) * | 1985-10-08 | 1989-09-05 | Lever Brothers Company | Detergent compositions containing fatty acid soap and monoesters of dicarboxylic acids |
US5002680A (en) * | 1985-03-01 | 1991-03-26 | The Procter & Gamble Company | Mild skin cleansing aerosol mousse with skin feel and moisturization benefits |
US5076953A (en) * | 1985-05-13 | 1991-12-31 | The Procter & Gamble Company | Skin cleansing synbars with low moisture and/or selected polymeric skin mildness aids |
US5730839A (en) * | 1995-07-21 | 1998-03-24 | Kimberly-Clark Worldwide, Inc. | Method of creping tissue webs containing a softener using a closed creping pocket |
US20050233929A1 (en) * | 2003-07-14 | 2005-10-20 | Ici Americas, Inc. | Solvated nonionic surfactants and fatty acids |
WO2008030312A1 (en) * | 2006-09-08 | 2008-03-13 | Millennium Specialty Chemicals, Inc. | Aqueous compositions containing monoester salts |
US20220249347A1 (en) * | 2021-02-10 | 2022-08-11 | TRI-K Industries, Inc. | Composition and Method Containing Pea and Quinoa Natural Peptides And Niacinamide to Enhance Skin Glow, Radiance And Even Skin Tone |
-
1971
- 1971-01-25 US US109614A patent/US3703481A/en not_active Expired - Lifetime
- 1971-11-12 CA CA127454A patent/CA938557A/en not_active Expired
Cited By (30)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3996148A (en) * | 1974-07-25 | 1976-12-07 | Pierre Fusey | Basic detergent for liquid lyes |
US4306997A (en) * | 1976-01-16 | 1981-12-22 | Lever Brothers Company | Foam bath compositions containing anionic detergent and monoglyceride |
US4101293A (en) * | 1977-03-30 | 1978-07-18 | Reichhold Chemicals, Inc. | Stabilizing emulsifiers |
FR2432309A1 (en) * | 1978-07-31 | 1980-02-29 | Kao Corp | COMPOSITION FOR RINSING HAIR BASED ON A SUCCINIC ACID DERIVATIVE AND A QUATERNARY AMMONIUM SALT |
US4406664A (en) * | 1980-01-22 | 1983-09-27 | Gulf & Western Industries, Inc. | Process for the enhanced separation of impurities from coal and coal products produced therefrom |
US4412843A (en) * | 1980-01-22 | 1983-11-01 | Gulf & Western Industries, Inc. | Beneficiated coal, coal mixtures and processes for the production thereof |
US4536372A (en) * | 1980-01-22 | 1985-08-20 | The Standard Oil Company | Apparatus for beneficiating coal |
US4304573A (en) * | 1980-01-22 | 1981-12-08 | Gulf & Western Industries, Inc. | Process of beneficiating coal and product |
US4358293A (en) * | 1981-01-29 | 1982-11-09 | Gulf & Western Manufacturing Co. | Coal-aqueous mixtures |
US4583990A (en) * | 1981-01-29 | 1986-04-22 | The Standard Oil Company | Method for the beneficiation of low rank coal |
US4430245A (en) | 1981-04-06 | 1984-02-07 | Internationale Octrooi Maatschappij "Octropa" B.V. | Soap composition |
US4526585A (en) * | 1981-05-28 | 1985-07-02 | The Standard Oil Company | Beneficiated coal, coal mixtures and processes for the production thereof |
US4462981A (en) * | 1982-12-10 | 1984-07-31 | Creative Products Resource, Associates Ltd. | Cosmetic applicator useful for skin moisturizing and deodorizing |
US4550035A (en) * | 1982-12-10 | 1985-10-29 | Creative Products Resource Associates, Ltd. | Cosmetic applicator useful for skin moisturizing and deodorizing |
US5002680A (en) * | 1985-03-01 | 1991-03-26 | The Procter & Gamble Company | Mild skin cleansing aerosol mousse with skin feel and moisturization benefits |
US4673525A (en) * | 1985-05-13 | 1987-06-16 | The Procter & Gamble Company | Ultra mild skin cleansing composition |
US4812253A (en) * | 1985-05-13 | 1989-03-14 | The Procter & Gamble Company | Ultra mild skin cleansing composition |
US5076953A (en) * | 1985-05-13 | 1991-12-31 | The Procter & Gamble Company | Skin cleansing synbars with low moisture and/or selected polymeric skin mildness aids |
US4863628A (en) * | 1985-10-08 | 1989-09-05 | Lever Brothers Company | Detergent compositions containing fatty acid soap and monoesters of dicarboxylic acids |
EP0259843A3 (en) * | 1986-09-09 | 1988-08-03 | S.C. Johnson & Son, Inc. | Post-foaming gel with an unsaturated or non-linear dialkanolamide or a monoalkanolamide |
EP0259843A2 (en) * | 1986-09-09 | 1988-03-16 | S.C. Johnson & Son, Inc. | Post-foaming gel with an unsaturated or non-linear dialkanolamide or a monoalkanolamide |
US5730839A (en) * | 1995-07-21 | 1998-03-24 | Kimberly-Clark Worldwide, Inc. | Method of creping tissue webs containing a softener using a closed creping pocket |
US20050233929A1 (en) * | 2003-07-14 | 2005-10-20 | Ici Americas, Inc. | Solvated nonionic surfactants and fatty acids |
US7479473B2 (en) * | 2003-07-14 | 2009-01-20 | Croda Uniqema, Inc. | Solvated nonionic surfactants and fatty acids |
US20090105106A1 (en) * | 2003-07-14 | 2009-04-23 | Croda Uniquema, Inc. | Solvated non-ionic surfactants and fatty acids |
US7754674B2 (en) | 2003-07-14 | 2010-07-13 | Croda Americas Llc | Solvated non-ionic surfactants and fatty acids |
WO2008030312A1 (en) * | 2006-09-08 | 2008-03-13 | Millennium Specialty Chemicals, Inc. | Aqueous compositions containing monoester salts |
US20080085933A1 (en) * | 2006-09-08 | 2008-04-10 | Erman Mark B | Aqueous compositions containing monoester salts |
US7652067B2 (en) | 2006-09-08 | 2010-01-26 | Millenium Specialty Chemicals, Inc. | Aqueous compositions containing monoester salts |
US20220249347A1 (en) * | 2021-02-10 | 2022-08-11 | TRI-K Industries, Inc. | Composition and Method Containing Pea and Quinoa Natural Peptides And Niacinamide to Enhance Skin Glow, Radiance And Even Skin Tone |
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