MXPA99011743A - Gel deodorant compositions having reduced skin irritation - Google Patents
Gel deodorant compositions having reduced skin irritationInfo
- Publication number
- MXPA99011743A MXPA99011743A MXPA/A/1999/011743A MX9911743A MXPA99011743A MX PA99011743 A MXPA99011743 A MX PA99011743A MX 9911743 A MX9911743 A MX 9911743A MX PA99011743 A MXPA99011743 A MX PA99011743A
- Authority
- MX
- Mexico
- Prior art keywords
- weight
- glycol
- composition
- deodorant
- polymeric
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 154
- 239000002781 deodorant agent Substances 0.000 title claims abstract description 86
- 230000036556 skin irritation Effects 0.000 title abstract description 5
- 231100000475 skin irritation Toxicity 0.000 title abstract description 5
- 206010040880 Skin irritation Diseases 0.000 title abstract description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims abstract description 41
- 239000003349 gelling agent Substances 0.000 claims abstract description 36
- 239000003205 fragrance Substances 0.000 claims abstract description 35
- 125000004432 carbon atoms Chemical group C* 0.000 claims abstract description 19
- PEDCQBHIVMGVHV-UHFFFAOYSA-N glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims abstract description 15
- 230000000699 topical Effects 0.000 claims abstract description 14
- XEFQLINVKFYRCS-UHFFFAOYSA-N Triclosan Chemical compound OC1=CC(Cl)=CC=C1OC1=CC=C(Cl)C=C1Cl XEFQLINVKFYRCS-UHFFFAOYSA-N 0.000 claims abstract description 12
- 229960003500 triclosan Drugs 0.000 claims abstract description 12
- ICUTUKXCWQYESQ-UHFFFAOYSA-N Triclocarban Chemical compound C1=CC(Cl)=CC=C1NC(=O)NC1=CC=C(Cl)C(Cl)=C1 ICUTUKXCWQYESQ-UHFFFAOYSA-N 0.000 claims abstract description 11
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims abstract description 11
- 229960001325 triclocarban Drugs 0.000 claims abstract description 10
- 235000011187 glycerol Nutrition 0.000 claims abstract description 9
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 8
- 239000002537 cosmetic Substances 0.000 claims abstract description 6
- 230000001276 controlling effect Effects 0.000 claims abstract description 3
- -1 fatty acid salt Chemical class 0.000 claims description 34
- 210000003491 Skin Anatomy 0.000 claims description 19
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 19
- 239000000194 fatty acid Substances 0.000 claims description 19
- 150000001298 alcohols Chemical class 0.000 claims description 12
- 239000011780 sodium chloride Substances 0.000 claims description 11
- SZXQTJUDPRGNJN-UHFFFAOYSA-N Dipropylene glycol Chemical compound OCCCOCCCO SZXQTJUDPRGNJN-UHFFFAOYSA-N 0.000 claims description 9
- MTHSVFCYNBDYFN-UHFFFAOYSA-N Diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 claims description 8
- 230000001877 deodorizing Effects 0.000 claims description 8
- 229920001223 polyethylene glycol Polymers 0.000 claims description 8
- 229940015975 1,2-hexanediol Drugs 0.000 claims description 4
- QVHMSMOUDQXMRS-UHFFFAOYSA-N 2-[2-[2-(2-hydroxypropoxy)propoxy]propoxy]propan-1-ol Chemical compound CC(O)COC(C)COC(C)COC(C)CO QVHMSMOUDQXMRS-UHFFFAOYSA-N 0.000 claims description 4
- 239000002202 Polyethylene glycol Substances 0.000 claims description 4
- RYYKJJJTJZKILX-UHFFFAOYSA-M Sodium stearate Chemical compound [Na+].CCCCCCCCCCCCCCCCCC([O-])=O RYYKJJJTJZKILX-UHFFFAOYSA-M 0.000 claims description 4
- FHKSXSQHXQEMOK-UHFFFAOYSA-N hexane-1,2-diol Chemical compound CCCCC(O)CO FHKSXSQHXQEMOK-UHFFFAOYSA-N 0.000 claims description 4
- YPFDHNVEDLHUCE-UHFFFAOYSA-N 1,3-Propanediol Chemical compound OCCCO YPFDHNVEDLHUCE-UHFFFAOYSA-N 0.000 claims description 3
- XXJWXESWEXIICW-UHFFFAOYSA-N 2-(2-Ethoxyethoxy)ethanol Chemical compound CCOCCOCCO XXJWXESWEXIICW-UHFFFAOYSA-N 0.000 claims description 3
- SVTBMSDMJJWYQN-UHFFFAOYSA-N 2-Methyl-2,4-pentanediol Chemical compound CC(O)CC(C)(C)O SVTBMSDMJJWYQN-UHFFFAOYSA-N 0.000 claims description 3
- LCZVSXRMYJUNFX-UHFFFAOYSA-N 2-[2-(2-hydroxypropoxy)propoxy]propan-1-ol Chemical compound CC(O)COC(C)COC(C)CO LCZVSXRMYJUNFX-UHFFFAOYSA-N 0.000 claims description 3
- 239000004743 Polypropylene Substances 0.000 claims description 3
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N Triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 claims description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 3
- 229940051250 hexylene glycol Drugs 0.000 claims description 3
- 229920001155 polypropylene Polymers 0.000 claims description 3
- MQOCIYICOGDBSG-UHFFFAOYSA-M potassium;hexadecanoate Chemical compound [K+].CCCCCCCCCCCCCCCC([O-])=O MQOCIYICOGDBSG-UHFFFAOYSA-M 0.000 claims description 3
- UWHCKJMYHZGTIT-UHFFFAOYSA-N tetraethylene glycol Chemical compound OCCOCCOCCOCCO UWHCKJMYHZGTIT-UHFFFAOYSA-N 0.000 claims description 3
- 229940114930 POTASSIUM STEARATE Drugs 0.000 claims description 2
- 229940080350 SODIUM STEARATE Drugs 0.000 claims description 2
- 229940045870 Sodium Palmitate Drugs 0.000 claims description 2
- BTURAGWYSMTVOW-UHFFFAOYSA-M Sodium laurate Chemical compound [Na+].CCCCCCCCCCCC([O-])=O BTURAGWYSMTVOW-UHFFFAOYSA-M 0.000 claims description 2
- 229940082004 Sodium laurate Drugs 0.000 claims description 2
- 229940075557 diethylene glycol monoethyl ether Drugs 0.000 claims description 2
- ANBFRLKBEIFNQU-UHFFFAOYSA-M potassium;octadecanoate Chemical compound [K+].CCCCCCCCCCCCCCCCCC([O-])=O ANBFRLKBEIFNQU-UHFFFAOYSA-M 0.000 claims description 2
- 229940045845 sodium myristate Drugs 0.000 claims description 2
- CVYDEWKUJFCYJO-UHFFFAOYSA-M sodium;docosanoate Chemical compound [Na+].CCCCCCCCCCCCCCCCCCCCCC([O-])=O CVYDEWKUJFCYJO-UHFFFAOYSA-M 0.000 claims description 2
- GGXKEBACDBNFAF-UHFFFAOYSA-M sodium;hexadecanoate Chemical compound [Na+].CCCCCCCCCCCCCCCC([O-])=O GGXKEBACDBNFAF-UHFFFAOYSA-M 0.000 claims description 2
- MRQYKJNZWPCFNB-UHFFFAOYSA-M sodium;icosanoate Chemical compound [Na+].CCCCCCCCCCCCCCCCCCCC([O-])=O MRQYKJNZWPCFNB-UHFFFAOYSA-M 0.000 claims description 2
- JUQGWKYSEXPRGL-UHFFFAOYSA-M sodium;tetradecanoate Chemical compound [Na+].CCCCCCCCCCCCCC([O-])=O JUQGWKYSEXPRGL-UHFFFAOYSA-M 0.000 claims description 2
- PYJBVGYZXWPIKK-UHFFFAOYSA-M potassium;tetradecanoate Chemical compound [K+].CCCCCCCCCCCCCC([O-])=O PYJBVGYZXWPIKK-UHFFFAOYSA-M 0.000 claims 1
- 230000035807 sensation Effects 0.000 claims 1
- 239000000499 gel Substances 0.000 description 52
- 125000000217 alkyl group Chemical group 0.000 description 18
- 125000003545 alkoxy group Chemical group 0.000 description 15
- 239000000463 material Substances 0.000 description 15
- 125000003118 aryl group Chemical group 0.000 description 14
- 239000001257 hydrogen Substances 0.000 description 14
- 229910052739 hydrogen Inorganic materials 0.000 description 14
- 125000003342 alkenyl group Chemical group 0.000 description 11
- 150000002431 hydrogen Chemical class 0.000 description 11
- 235000019645 odor Nutrition 0.000 description 11
- 239000002304 perfume Substances 0.000 description 11
- 239000002904 solvent Substances 0.000 description 11
- 150000004665 fatty acids Chemical class 0.000 description 10
- DNIAPMSPPWPWGF-UHFFFAOYSA-N propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 10
- 150000005215 alkyl ethers Chemical class 0.000 description 9
- 125000004356 hydroxy functional group Chemical group O* 0.000 description 9
- 125000005907 alkyl ester group Chemical group 0.000 description 7
- 239000004615 ingredient Substances 0.000 description 7
- 239000000126 substance Substances 0.000 description 7
- ULQISTXYYBZJSJ-UHFFFAOYSA-N 12-hydroxyoctadecanoic acid Chemical compound CCCCCCC(O)CCCCCCCCCCC(O)=O ULQISTXYYBZJSJ-UHFFFAOYSA-N 0.000 description 6
- 229940114072 12-hydroxystearic acid Drugs 0.000 description 6
- 239000002253 acid Substances 0.000 description 6
- 125000002877 alkyl aryl group Chemical group 0.000 description 6
- 150000001408 amides Chemical class 0.000 description 6
- 125000004122 cyclic group Chemical group 0.000 description 6
- 229910052799 carbon Inorganic materials 0.000 description 5
- 239000007788 liquid Substances 0.000 description 5
- 229910052757 nitrogen Inorganic materials 0.000 description 5
- 150000003839 salts Chemical class 0.000 description 5
- 125000005373 siloxane group Chemical group [SiH2](O*)* 0.000 description 5
- 239000000796 flavoring agent Substances 0.000 description 4
- 235000019634 flavors Nutrition 0.000 description 4
- 238000009472 formulation Methods 0.000 description 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 4
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- UKMSUNONTOPOIO-UHFFFAOYSA-N Behenic acid Chemical compound CCCCCCCCCCCCCCCCCCCCCC(O)=O UKMSUNONTOPOIO-UHFFFAOYSA-N 0.000 description 3
- 125000001843 C4-C10 alkenyl group Chemical group 0.000 description 3
- 229920001451 Polypropylene glycol Polymers 0.000 description 3
- QIQXTHQIDYTFRH-UHFFFAOYSA-N Stearic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 3
- 150000001299 aldehydes Chemical class 0.000 description 3
- 229910052782 aluminium Inorganic materials 0.000 description 3
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminum Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 3
- 239000004599 antimicrobial Substances 0.000 description 3
- WVDDGKGOMKODPV-UHFFFAOYSA-N benzyl alcohol Chemical compound OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 230000000873 masking Effects 0.000 description 3
- 239000003921 oil Substances 0.000 description 3
- 235000019198 oils Nutrition 0.000 description 3
- 159000000001 potassium salts Chemical class 0.000 description 3
- 159000000000 sodium salts Chemical class 0.000 description 3
- WERYXYBDKMZEQL-UHFFFAOYSA-N 1,4-Butanediol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 2
- BACYUWVYYTXETD-UHFFFAOYSA-N 2-[dodecanoyl(methyl)amino]acetic acid Chemical compound CCCCCCCCCCCC(=O)N(C)CC(O)=O BACYUWVYYTXETD-UHFFFAOYSA-N 0.000 description 2
- 235000007173 Abies balsamea Nutrition 0.000 description 2
- POJWUDADGALRAB-PVQJCKRUSA-N Allantoin Natural products NC(=O)N[C@@H]1NC(=O)NC1=O POJWUDADGALRAB-PVQJCKRUSA-N 0.000 description 2
- BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical class OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 description 2
- WWZKQHOCKIZLMA-UHFFFAOYSA-N Caprylic acid Chemical compound CCCCCCCC(O)=O WWZKQHOCKIZLMA-UHFFFAOYSA-N 0.000 description 2
- 235000019499 Citrus oil Nutrition 0.000 description 2
- ZYGHJZDHTFUPRJ-UHFFFAOYSA-N Coumarin Chemical compound C1=CC=C2OC(=O)C=CC2=C1 ZYGHJZDHTFUPRJ-UHFFFAOYSA-N 0.000 description 2
- 244000018716 Impatiens biflora Species 0.000 description 2
- 235000015912 Impatiens biflora Nutrition 0.000 description 2
- KDXKERNSBIXSRK-YFKPBYRVSA-N L-lysine Chemical compound NCCCC[C@H](N)C(O)=O KDXKERNSBIXSRK-YFKPBYRVSA-N 0.000 description 2
- POULHZVOKOAJMA-UHFFFAOYSA-N Lauric acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 2
- WRMNZCZEMHIOCP-UHFFFAOYSA-N Phenethyl alcohol Chemical compound OCCC1=CC=CC=C1 WRMNZCZEMHIOCP-UHFFFAOYSA-N 0.000 description 2
- KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Chemical compound OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 2
- MWOOGOJBHIARFG-UHFFFAOYSA-N Vanillin Chemical compound COC1=CC(C=O)=CC=C1O MWOOGOJBHIARFG-UHFFFAOYSA-N 0.000 description 2
- 239000011358 absorbing material Substances 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 229910052783 alkali metal Inorganic materials 0.000 description 2
- 150000001340 alkali metals Chemical class 0.000 description 2
- 125000002947 alkylene group Chemical group 0.000 description 2
- 230000001166 anti-perspirant Effects 0.000 description 2
- 239000003213 antiperspirant Substances 0.000 description 2
- 235000019437 butane-1,3-diol Nutrition 0.000 description 2
- PUPZLCDOIYMWBV-UHFFFAOYSA-N butylene glycol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 description 2
- 239000010500 citrus oil Substances 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 239000000284 extract Substances 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 229910001385 heavy metal Inorganic materials 0.000 description 2
- 150000001261 hydroxy acids Chemical class 0.000 description 2
- UGAGPNKCDRTDHP-UHFFFAOYSA-N juniperic acid Chemical compound OCCCCCCCCCCCCCCCC(O)=O UGAGPNKCDRTDHP-UHFFFAOYSA-N 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 2
- 229910052700 potassium Inorganic materials 0.000 description 2
- 239000011591 potassium Substances 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 239000001294 propane Substances 0.000 description 2
- FGVVTMRZYROCTH-UHFFFAOYSA-N pyridine-2-thiol N-oxide Chemical class [O-][N+]1=CC=CC=C1S FGVVTMRZYROCTH-UHFFFAOYSA-N 0.000 description 2
- 229960002026 pyrithione Drugs 0.000 description 2
- KEAYESYHFKHZAL-UHFFFAOYSA-N sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 239000000341 volatile oil Substances 0.000 description 2
- 239000000260 (2E,6E)-3,7,11-trimethyldodeca-2,6,10-trien-1-ol Substances 0.000 description 1
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 description 1
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 description 1
- 239000001244 (E)-1-(2,6,6-trimethyl-1-cyclohex-2-enyl)pent-1-en-3-one Substances 0.000 description 1
- 239000001124 (E)-prop-1-ene-1,2,3-tricarboxylic acid Substances 0.000 description 1
- 229940058015 1,3-butylene glycol Drugs 0.000 description 1
- VPKMGDRERYMTJX-CMDGGOBGSA-N 1-(2,6,6-Trimethyl-2-cyclohexen-1-yl)-1-penten-3-one Chemical compound CCC(=O)\C=C\C1C(C)=CCCC1(C)C VPKMGDRERYMTJX-CMDGGOBGSA-N 0.000 description 1
- GDXHBFHOEYVPED-UHFFFAOYSA-N 1-(2-butoxyethoxy)butane Chemical compound CCCCOCCOCCCC GDXHBFHOEYVPED-UHFFFAOYSA-N 0.000 description 1
- DURPTKYDGMDSBL-UHFFFAOYSA-N 1-butoxybutane Chemical class CCCCOCCCC DURPTKYDGMDSBL-UHFFFAOYSA-N 0.000 description 1
- HANWHVWXFQSQGJ-UHFFFAOYSA-N 1-tetradecoxytetradecane Chemical class CCCCCCCCCCCCCCOCCCCCCCCCCCCCC HANWHVWXFQSQGJ-UHFFFAOYSA-N 0.000 description 1
- ASTZGOKPQNQZHQ-UHFFFAOYSA-N 12-hydroxy-N,N-di(propan-2-yl)octadecanamide Chemical compound CCCCCCC(O)CCCCCCCCCCC(=O)N(C(C)C)C(C)C ASTZGOKPQNQZHQ-UHFFFAOYSA-N 0.000 description 1
- ZDHCZVWCTKTBRY-UHFFFAOYSA-N 12-hydroxylauric acid Chemical compound OCCCCCCCCCCCC(O)=O ZDHCZVWCTKTBRY-UHFFFAOYSA-N 0.000 description 1
- DUFKCOQISQKSAV-UHFFFAOYSA-N 2-(2-hydroxypropoxy)propan-1-ol Chemical group CC(O)COC(C)CO DUFKCOQISQKSAV-UHFFFAOYSA-N 0.000 description 1
- NFAVNWJJYQAGNB-UHFFFAOYSA-N 2-Methylundecanal Chemical compound CCCCCCCCCC(C)C=O NFAVNWJJYQAGNB-UHFFFAOYSA-N 0.000 description 1
- HMKKIXGYKWDQSV-SDNWHVSQSA-N 2-Pentyl-3-phenyl-2-propenal Chemical compound CCCCC\C(C=O)=C/C1=CC=CC=C1 HMKKIXGYKWDQSV-SDNWHVSQSA-N 0.000 description 1
- CCRSXTUSQOIQSX-UHFFFAOYSA-N 2-dodecyl-N,N'-dihexylbutanediamide Chemical compound CCCCCCCCCCCCC(C(=O)NCCCCCC)CC(=O)NCCCCCC CCRSXTUSQOIQSX-UHFFFAOYSA-N 0.000 description 1
- UXJMXERXJQAWSP-UHFFFAOYSA-N 2-pentylcyclohexan-1-one Chemical compound CCCCCC1CCCCC1=O UXJMXERXJQAWSP-UHFFFAOYSA-N 0.000 description 1
- ZOZIRNMDEZKZHM-UHFFFAOYSA-N 2-phenylethyl 2-phenylacetate Chemical compound C=1C=CC=CC=1CCOC(=O)CC1=CC=CC=C1 ZOZIRNMDEZKZHM-UHFFFAOYSA-N 0.000 description 1
- KRKNYBCHXYNGOX-UHFFFAOYSA-K 2qpq Chemical class [O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O KRKNYBCHXYNGOX-UHFFFAOYSA-K 0.000 description 1
- PMGCQNGBLMMXEW-UHFFFAOYSA-N 3-methylbutyl 2-hydroxybenzoate Chemical compound CC(C)CCOC(=O)C1=CC=CC=C1O PMGCQNGBLMMXEW-UHFFFAOYSA-N 0.000 description 1
- DCSKAMGZSIRJAQ-UHFFFAOYSA-N 4-(2-methylbutan-2-yl)cyclohexan-1-one Chemical compound CCC(C)(C)C1CCC(=O)CC1 DCSKAMGZSIRJAQ-UHFFFAOYSA-N 0.000 description 1
- 229940091181 Aconitic Acid Drugs 0.000 description 1
- GTZCVFVGUGFEME-UHFFFAOYSA-N Aconitic acid Chemical compound OC(=O)CC(C(O)=O)=CC(O)=O GTZCVFVGUGFEME-UHFFFAOYSA-N 0.000 description 1
- 229960000458 Allantoin Drugs 0.000 description 1
- 244000144927 Aloe barbadensis Species 0.000 description 1
- 235000002961 Aloe barbadensis Nutrition 0.000 description 1
- 239000004857 Balsam Substances 0.000 description 1
- JPYQFYIEOUVJDU-UHFFFAOYSA-N Beclamide Chemical compound ClCCC(=O)NCC1=CC=CC=C1 JPYQFYIEOUVJDU-UHFFFAOYSA-N 0.000 description 1
- 235000021357 Behenic acid Nutrition 0.000 description 1
- 229960001950 Benzethonium Chloride Drugs 0.000 description 1
- UREZNYTWGJKWBI-UHFFFAOYSA-M Benzethonium chloride Chemical compound [Cl-].C1=CC(C(C)(C)CC(C)(C)C)=CC=C1OCCOCC[N+](C)(C)CC1=CC=CC=C1 UREZNYTWGJKWBI-UHFFFAOYSA-M 0.000 description 1
- ISAOCJYIOMOJEB-UHFFFAOYSA-N Benzoin Chemical compound C=1C=CC=CC=1C(O)C(=O)C1=CC=CC=C1 ISAOCJYIOMOJEB-UHFFFAOYSA-N 0.000 description 1
- 229960002130 Benzoin Drugs 0.000 description 1
- ZCTQGTTXIYCGGC-UHFFFAOYSA-N Benzyl salicylate Chemical compound OC1=CC=CC=C1C(=O)OCC1=CC=CC=C1 ZCTQGTTXIYCGGC-UHFFFAOYSA-N 0.000 description 1
- 239000004135 Bone phosphate Substances 0.000 description 1
- 125000004399 C1-C4 alkenyl group Chemical group 0.000 description 1
- DSSYKIVIOFKYAU-UHFFFAOYSA-N Camphor Chemical compound C1CC2(C)C(=O)CC1C2(C)C DSSYKIVIOFKYAU-UHFFFAOYSA-N 0.000 description 1
- 229960000846 Camphor Drugs 0.000 description 1
- 239000005635 Caprylic acid (CAS 124-07-2) Substances 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate dianion Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- 241001090476 Castoreum Species 0.000 description 1
- 241000723346 Cinnamomum camphora Species 0.000 description 1
- 239000011703 D-panthenol Substances 0.000 description 1
- SNPLKNRPJHDVJA-ZETCQYMHSA-N D-panthenol Chemical compound OCC(C)(C)[C@@H](O)C(=O)NCCCO SNPLKNRPJHDVJA-ZETCQYMHSA-N 0.000 description 1
- 235000004866 D-panthenol Nutrition 0.000 description 1
- KSMVZQYAVGTKIV-UHFFFAOYSA-N Decanal Chemical compound CCCCCCCCCC=O KSMVZQYAVGTKIV-UHFFFAOYSA-N 0.000 description 1
- 229960003949 Dexpanthenol Drugs 0.000 description 1
- FLKPEMZONWLCSK-UHFFFAOYSA-N Diethyl phthalate Chemical compound CCOC(=O)C1=CC=CC=C1C(=O)OCC FLKPEMZONWLCSK-UHFFFAOYSA-N 0.000 description 1
- USIUVYZYUHIAEV-UHFFFAOYSA-N Diphenyl ether Chemical compound C=1C=CC=CC=1OC1=CC=CC=C1 USIUVYZYUHIAEV-UHFFFAOYSA-N 0.000 description 1
- HFJRKMMYBMWEAD-UHFFFAOYSA-N Dodecanal Chemical compound CCCCCCCCCCCC=O HFJRKMMYBMWEAD-UHFFFAOYSA-N 0.000 description 1
- 206010064503 Excessive skin Diseases 0.000 description 1
- CRDAMVZIKSXKFV-YFVJMOTDSA-N Farnesol Chemical compound CC(C)=CCC\C(C)=C\CC\C(C)=C\CO CRDAMVZIKSXKFV-YFVJMOTDSA-N 0.000 description 1
- 229940043259 Farnesol Drugs 0.000 description 1
- 241000208152 Geranium Species 0.000 description 1
- 241000282375 Herpestidae Species 0.000 description 1
- 229940060367 Inert Ingredients Drugs 0.000 description 1
- SFEOKXHPFMOVRM-BQYQJAHWSA-N Ionone Chemical compound CC(=O)\C=C\C1C(=C)CCCC1(C)C SFEOKXHPFMOVRM-BQYQJAHWSA-N 0.000 description 1
- LVHBHZANLOWSRM-UHFFFAOYSA-N Itaconic acid Chemical compound OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 1
- 235000019766 L-Lysine Nutrition 0.000 description 1
- 239000004166 Lanolin Substances 0.000 description 1
- 229940039717 Lanolin Drugs 0.000 description 1
- 239000005639 Lauric acid Substances 0.000 description 1
- 239000004472 Lysine Substances 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- 240000009136 Monarda didyma Species 0.000 description 1
- 235000010672 Monarda didyma Nutrition 0.000 description 1
- TUNFSRHWOTWDNC-UHFFFAOYSA-N Myristic acid Chemical compound CCCCCCCCCCCCCC(O)=O TUNFSRHWOTWDNC-UHFFFAOYSA-N 0.000 description 1
- UHUFTBALEZWWIH-UHFFFAOYSA-N Myristyl aldehyde Chemical compound CCCCCCCCCCCCCC=O UHUFTBALEZWWIH-UHFFFAOYSA-N 0.000 description 1
- LUUVYNAGDYDILD-UHFFFAOYSA-N N',N'-dibutylbutanediamide Chemical compound CCCCN(CCCC)C(=O)CCC(N)=O LUUVYNAGDYDILD-UHFFFAOYSA-N 0.000 description 1
- DYUGTPXLDJQBRB-UHFFFAOYSA-N N-myristoylglycine Chemical compound CCCCCCCCCCCCCC(=O)NCC(O)=O DYUGTPXLDJQBRB-UHFFFAOYSA-N 0.000 description 1
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- 235000019482 Palm oil Nutrition 0.000 description 1
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- 239000002250 absorbent Substances 0.000 description 1
- 125000002252 acyl group Chemical group 0.000 description 1
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- 150000001342 alkaline earth metals Chemical class 0.000 description 1
- 235000011399 aloe vera Nutrition 0.000 description 1
- YAKZEVHORUHNLS-UHFFFAOYSA-K aluminum;sodium;2-hydroxypropanoate;chloride;hydroxide;hydrate Chemical compound O.[OH-].[Na+].[Al+3].[Cl-].CC(O)C([O-])=O YAKZEVHORUHNLS-UHFFFAOYSA-K 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- NLXLAEXVIDQMFP-UHFFFAOYSA-N ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 1
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- 239000003242 anti bacterial agent Substances 0.000 description 1
- 230000000845 anti-microbial Effects 0.000 description 1
- 239000003429 antifungal agent Substances 0.000 description 1
- 239000012298 atmosphere Substances 0.000 description 1
- 235000021302 avocado oil Nutrition 0.000 description 1
- 239000008163 avocado oil Substances 0.000 description 1
- 235000013871 bee wax Nutrition 0.000 description 1
- 235000015278 beef Nutrition 0.000 description 1
- 239000012166 beeswax Substances 0.000 description 1
- 229940116226 behenic acid Drugs 0.000 description 1
- IUFDGAYUMGNOBT-UHFFFAOYSA-N benzyl 12-hydroxyoctadecanoate Chemical compound CCCCCCC(O)CCCCCCCCCCC(=O)OCC1=CC=CC=C1 IUFDGAYUMGNOBT-UHFFFAOYSA-N 0.000 description 1
- 235000019445 benzyl alcohol Nutrition 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 229930007890 camphor Natural products 0.000 description 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 1
- 150000001244 carboxylic acid anhydrides Chemical class 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
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- 229920001577 copolymer Polymers 0.000 description 1
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- 229960000956 coumarin Drugs 0.000 description 1
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- 235000013399 edible fruits Nutrition 0.000 description 1
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- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 229930002886 farnesol Natural products 0.000 description 1
- 239000003925 fat Substances 0.000 description 1
- 235000019197 fats Nutrition 0.000 description 1
- 235000021323 fish oil Nutrition 0.000 description 1
- 235000019717 geranium oil Nutrition 0.000 description 1
- 239000010648 geranium oil Substances 0.000 description 1
- CTKINSOISVBQLD-UHFFFAOYSA-N glycidol Chemical compound OCC1CO1 CTKINSOISVBQLD-UHFFFAOYSA-N 0.000 description 1
- 235000019382 gum benzoic Nutrition 0.000 description 1
- DWYTXBVHIIANQN-UHFFFAOYSA-N hexadecylazanide Chemical compound CCCCCCCCCCCCCCCC[NH-] DWYTXBVHIIANQN-UHFFFAOYSA-N 0.000 description 1
- ZWVMLYRJXORSEP-UHFFFAOYSA-N hexane-1,2,6-triol Chemical compound OCCCCC(O)CO ZWVMLYRJXORSEP-UHFFFAOYSA-N 0.000 description 1
- 239000003906 humectant Substances 0.000 description 1
- 125000004435 hydrogen atoms Chemical group [H]* 0.000 description 1
- 229930002839 ionones Natural products 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 235000019388 lanolin Nutrition 0.000 description 1
- 229960003646 lysine Drugs 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- RVWOWEQKPMPWMQ-UHFFFAOYSA-N methyl 12-hydroxyoctadecanoate Chemical compound CCCCCCC(O)CCCCCCCCCCC(=O)OC RVWOWEQKPMPWMQ-UHFFFAOYSA-N 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000006011 modification reaction Methods 0.000 description 1
- MGFYIUFZLHCRTH-UHFFFAOYSA-N nitrilotriacetic acid Chemical compound OC(=O)CN(CC(O)=O)CC(O)=O MGFYIUFZLHCRTH-UHFFFAOYSA-N 0.000 description 1
- 229960002446 octanoic acid Drugs 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid group Chemical group C(CCCCCCC\C=C/CCCCCCCC)(=O)O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- 239000004006 olive oil Substances 0.000 description 1
- 235000008390 olive oil Nutrition 0.000 description 1
- FTXUQEKXCJSWMO-UHFFFAOYSA-N oxecan-2-one Chemical compound O=C1CCCCCCCCO1 FTXUQEKXCJSWMO-UHFFFAOYSA-N 0.000 description 1
- OTGHWLKHGCENJV-UHFFFAOYSA-M oxirane-2-carboxylate Chemical compound [O-]C(=O)C1CO1 OTGHWLKHGCENJV-UHFFFAOYSA-M 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
- 239000000312 peanut oil Substances 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- XRMLOZSMCSUBTL-UHFFFAOYSA-N phenylazanide Chemical compound [NH-]C1=CC=CC=C1 XRMLOZSMCSUBTL-UHFFFAOYSA-N 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 239000001738 pogostemon cablin oil Substances 0.000 description 1
- 239000002798 polar solvent Substances 0.000 description 1
- 125000003367 polycyclic group Chemical group 0.000 description 1
- 229920005606 polypropylene copolymer Polymers 0.000 description 1
- XUWVIABDWDTJRZ-UHFFFAOYSA-N propan-2-ylazanide Chemical compound CC(C)[NH-] XUWVIABDWDTJRZ-UHFFFAOYSA-N 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 230000001105 regulatory Effects 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- YGSDEFSMJLZEOE-UHFFFAOYSA-M salicylate Chemical class OC1=CC=CC=C1C([O-])=O YGSDEFSMJLZEOE-UHFFFAOYSA-M 0.000 description 1
- 229960001860 salicylate Drugs 0.000 description 1
- FSYKKLYZXJSNPZ-UHFFFAOYSA-N sarcosine zwitterion Chemical compound C[NH2+]CC([O-])=O FSYKKLYZXJSNPZ-UHFFFAOYSA-N 0.000 description 1
- 230000035943 smell Effects 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- ADWNFGORSPBALY-UHFFFAOYSA-M sodium;2-[dodecyl(methyl)amino]acetate Chemical compound [Na+].CCCCCCCCCCCCN(C)CC([O-])=O ADWNFGORSPBALY-UHFFFAOYSA-M 0.000 description 1
- 239000003549 soybean oil Substances 0.000 description 1
- 235000012424 soybean oil Nutrition 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 125000003107 substituted aryl group Chemical group 0.000 description 1
- 239000001384 succinic acid Substances 0.000 description 1
- 238000010189 synthetic method Methods 0.000 description 1
- 239000003760 tallow Substances 0.000 description 1
- 239000001069 triethyl citrate Substances 0.000 description 1
- 235000013769 triethyl citrate Nutrition 0.000 description 1
- SZYJELPVAFJOGJ-UHFFFAOYSA-N trimethylamine hydrochloride Chemical compound Cl.CN(C)C SZYJELPVAFJOGJ-UHFFFAOYSA-N 0.000 description 1
- OFHHDSQXFXLTKC-UHFFFAOYSA-N undec-10-enal Chemical compound C=CCCCCCCCCC=O OFHHDSQXFXLTKC-UHFFFAOYSA-N 0.000 description 1
- 229940117960 vanillin Drugs 0.000 description 1
- 235000012141 vanillin Nutrition 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 230000000007 visual effect Effects 0.000 description 1
- 150000003751 zinc Chemical class 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 150000003754 zirconium Chemical class 0.000 description 1
- LUZDYPLAQQGJEA-UHFFFAOYSA-N Β-Naphthol methyl ether Chemical compound C1=CC=CC2=CC(OC)=CC=C21 LUZDYPLAQQGJEA-UHFFFAOYSA-N 0.000 description 1
Abstract
Disclosed are gel deodorant compositions comprising (a) from about 0.001%to about 50%by weight of a deodorant active, fragrance, or combination thereof;(b) from about 0.01%to about 20%by weight of a gellant;(c) from about 5%to about 90%by weight of a polymeric alcohol having at least one free hydroxyl group and also having from about 2 to about 80 alkoxylate radicals wherein in the alkoxylate radical contains from about 2 to about 6 carbon atoms;(d) from about 5%to about 89%by weight of a nonpolymeric alcohol having at least two free hydroxyl groups, and also having from about 4 to about 20 carbon atoms, wherein the weight ratio of the polymeric to nonpolymeric alcohol is from about 18:1 to about 1:5;(e) from zero percent to about 10%by weight of glycerin;and (f) from about 0.01%to about 89%by weight of water. Also disclosed is a method of controlling malodor associated with perspiration by topical application of any deodorant composition containing a select combination of triclosan and triclocarban. All of these compositions remain clear or translucent over extended periods of time, and provide little or no skin irritation in addition to improved cosmetic benefits such as dry feel, ease of application, emolliency, fragrance longevity, and no powdery residue.
Description
DEODORANT COMPOSITIONS IN GEL THAT HAVE ^ REDUCED LEVEL OF SKIN IRRITATION
FIELD OF THE INVENTION The present invention relates to gel deodorizing compositions that provide a reduced degree of skin irritation. In particular, the present invention relates to deodorant gel compositions containing a gelling agent, deodorant active or fragrance, and a select combination of a polymeric alcohol and non-polymeric alcohols.
BACKGROUND OF THE INVENTION __ Topical deodorants have been formulated in a variety of forms and are intended for topical application on human skin to mask or prevent odors associated with human perspiration.These topical deodorants are usually applied topically To the armpit or other area of the skin in the form of soft deodorant gels or sticks.These product forms usually contain a gelling agent, solvent and perfume or an antimicrobial active.
Fatty acid soaps are commonly used as gelling agents in topical deodorant gels, examples of which include sodium or potassium salts of naturally occurring fatty acids. In general, the gelling agent is used in combination with a highly polar alcohol solvent to provide aesthetic properties such as, for example, clarity, ease of application, moderately cold and cool feel in the application, lack of dusty residue, and dry feeling. Monohydric and dihydric alcohols, especially propylene glycol and dipropylene glycol, are often used for this purpose. Many types of gel deodorizing formulations are known, including those comprising fatty acid salts and a solvent such as, for example, water, monohydric alcohols, or dihydric alcohols. A typical example of this formulation are alcohol-containing gels comprising a fatty acid salt or other similar gelling agent, triclosan or other deodorant active and a polar solvent such as, for example, ethanol, propylene glycol, dipropylene glycol or other higher molecular weight polypropylene glycols. . Although these deodorant gels containing alcohol are very popular and are commonly used, many of them are also very strong for the skin and can cause excessive skin irritation after topical application. Therefore, it is an object of the present invention to provide a deodorant gel composition containing alcohol that is mild to the skin and causes minimal or no irritation therein, and furthermore provide a composition containing a select proportion of an alcohol. polymeric and non-polymeric alcohols. A further object of the present invention is to provide a composition having a dry feel and other improved cosmetic benefits such as, for example, ease of application, emolliency, fragrance durability and / or reduced level of visible residue.
BRIEF DESCRIPTION OF THE INVENTION The present invention is directed to gel deodorant compositions comprising from about (a) 0.001% to about 50% by weight of a deodorant active, fragrance, or combination thereof; (b) from about 0.01% to about 20% by weight of a gellant; (c) from about 5% to about 90% by weight of a polymeric alcohol having at least one free hydroxyl group and also having from about 2 to about 80 alkoxylated radicals, each having from about 2 to about 6 carbon atoms; carbon; (d) from about 5% to about 90% by weight of a non-polymeric alcohol having at least two free hydroxyl groups and also having from about 3 to about 20 carbon atoms, wherein the weight ratio of the polymeric alcohol to non-polymeric alcohol is from about 18: 1 to about 1: 5; (e) from zero percent to about 10% by weight of glycerin; and (f) from approximately 0.01% to approximately! 89% by weight ~ of water. It has been found that the deodorant gel compositions of the present invention are gentle to the skin and are associated with minimal or no irritation thereof. These compositions also remain substantially clear or translucent for long periods of time and provide improved cosmetic benefits such as for example dry feel, ease of application, emolliency, deodorant efficacy, fragrance durability and / or no dusty residue.
DETAILED DESCRIPTION OF THE INVENTION The gel deodorant compositions of the present invention comprise as essential ingredients a gelling agent, a polymeric alcohol, a non-polymeric alcohol and a perfume and / or deodorant active. These gel deodorant compositions are intended for topical application in the armpit or other suitable areas of the skin. Preferably, the gel deodorizing compositions are in the form of solid solid or soft bars, but may also be formulated in a variety of non-stick formulations suitable for application to the armpit or other area of the skin. The term "environmental conditions" in the sense in which it is used herein refers to the surrounding conditions under about one (1) atmosphere of pressure, at about 50% relative humidity, and at about 25 ° C. The gel deodorant compositions of the present invention may comprise, consist of, or consist essentially of essential elements and limitations of the invention described herein, as well as also any other additional or optional ingredients, components, or limitations described in I presented. - All percentages, parts and proportions are by weight of the total composition, unless otherwise specified. All weights as they pertain to the ingredients listed are based on the active level and, therefore, do not include solvents or by-products that may be included in commercially available materials unless otherwise specified.
DEODORANT ACTIVE AND FRAGRANCE The gel deodorant composition of the present invention comprises a deodorant active, fragment or combination thereof, including deodorant fragments, at concentrations ranging from about 0.001% to about 50%, preferably about 0.01. % to about 20%, more preferably from about 0.1% to about 10%, by weight of the composition. These active deodorants and perfumes include any deodorant or fragrance known or otherwise safe and effective for topical application to human skin. i Unless otherwise specified, the term "active" in the sense in which it is used herein generally refers to deodorant active or fragrances, while the term "deodorant active" specifically refers to materials topics that can avoid or eliminate bad smells that result in perspiration. The term "fragrance" in the sense in which it is used herein, specifically refers to any topical material that covers or masks odors that result from perspiration, or that otherwise gives the composition the aroma ^ of desired perfume.
a) Active Deodorant. Deodorant actives suitable for use in the gel deodorant composition include any topical material that is known or otherwise effective in preventing or eliminating odors associated with perspiration. These deodorant actives are typically antimicrobial agents (e.g., antibacterial agents, antifungal agents), malodor absorbing material, or combinations thereof. Preferred deodorant actives are antimicrobial agents, non-limiting examples of which include cet-1-t-rimet-ammonium bromide, cet-pyridinium chloride, benzethonium chloride, diisobutyl-2-phenoxy-ethoxy-2-yl-dimethyl chloride. -benzyl-ammonium, sodium N-lauryl sarcosine, sodium N-palmetil sarcosine, lauroyl sarcosine, N-myristoyl glycine, potassium N-lauryl sarcosine, trimethylammonium chloride, sodium-aluminum chlorhydroxy lactate, triethyl citrate, chloride ammonium of t ricet ilmet ilo, diphenyl ether of 2, 4, 4 '-t ricloro-2' -hydroxy (triclosan), 3,4,4'-trichlorocarbanilide (trichlocarbon), diaminoalkyl amides, such as, for example, hexadecyl amide of L-lysine, heavy metal salts of citrate, salicylate, and pyroctose, especially zinc salts, and acids thereof, heavy metal salts of pyrithione, especially pyrithione from jz-inc, zinc phenosulfate , farnesol, and combinations thereof. The preferred deodorizing actives are triclosan, triclocarban, and combinations thereof, wherein the preferred concentration of either triclosan or triclocarban ranges from about 0.01% to about 1.0%, more preferably about 0.1% about 0.5%, still of greater preferably from about 0.1% to about 0.3%, by weight of the composition, and wherein the total concentration of triclosan and trichlocarbon when used together in a composition ranges from about 0.01% to about 2.0%, more preferably about 0.2% to about 1.0%, still more preferably about 0.2% about 0.6%, in comparison to the compi-tion. It has been found that the combination of these two active deodorants provides deodorant efficacy that exceeds the cumulative deodorizing efficacy that one could otherwise predict from that combination. The preferred combination of triclosan and triclocarban is effective to provide improved deodorant performance from the deodorant compositions described herein, or from any known deodorant or topical composition containing this combination that is otherwise suitable for application to human skin Therefore, the invention herein is also directed to a method for controlling the malodour associated with human perspiration by topically applying the riclosan / triclocarban combination described above, or any other suitable composition containing the combination of triclosan / t riclocarbano described in the above, to the armpit or other area of the skin. From most of these deodorant compositions containing this combination, from about 0.1 grams to about 2.0 grams per armpit of the deodorant composition are applied, preferably once or twice "per day, most preferably once a day. Active deodorants include odor-absorbing materials, such as, for example, carbonate and bicarbonate salts, which include alkali metal, ammonium and tetraalkylammonium carbonates and bicarbonates.The sodium and potassium salts of these absorbent materials are preferred. Preferably, the anhydrous deodorant composition is practically free of astringent antiperspirant actives, such as, for example, astringent salts or aluminum or zirconium complexes. In this context, the term "practically free" means that the gel deodorant composition preferably contains less than about 5%, more preferably less than about 2%, still more preferably zero percent by weight of the astringent antiperspirant actives. ~~
b) Fragrance Fragrances suitable for use in the gel deodorant composition include any topical material which is known or otherwise effective in masking the malodor associated with perspiration, or which otherwise provides the composition with the desired perfume flavor . These fragrances include any perfume or chemical perfume compound suitable for topical application to the skin. The concentration of the fragrance in the gel composition must be effective to provide the desired aroma characteristics or to mask the malodor, where the malodour is inherently associated with the composition itself or is associated with the development of malodour from the human perspiration. Also, the fragrance and all the carriers that accompany it should not impart excessive itching to the skin, especially to cracked or irritated skin, at the levels previously described. The fragrance will typically be in the form of water-insoluble perfumes that are solubilized in the gel deodorant composition. The fragrances are made by those skilled in the art in a wide variety of fragrances and concentrations. Typical fragrances are described in Arctander, Perfume and Flavor Chemicals (Aroma Chemicals), Vol. I ~ and 11 (1969); and Arctahder, Perfume and Flavor Materials of Natural Origin (1960). U.S. Patent 4,322,308 and U.S. Patent 4,304,679, both incorporated herein by reference, describe fragrance components that generally include, but are not limited to: volatile phenolic substances (such as, for example, iso-amyl salicylate) , benzyl salicylate, and thymus red oil); essential oils (such as, for example, geranium oil, patchouli oil, and Tde petit flower oil); citrus oils; extracts and resins (such as, for example, Siamese benzoin resinoid and opoponaco resinoid); "synthetic" oils
(such as for example Bergamot 37 and 430, Geranium
76 and T? Omeransol 314); aldehydes and ketones (such as, for example, B-methyl naphthyl ketone, p-t-butyl-A-methyl hydroxycinnamic aldehyde and p-t-amyl cyclohexanone); polycyclic compounds (such as, for example, coumarin and ß-naphthyl methylether); esters (such as, for example, diethyl phthalate, phenylethyl phenylacetate, nonanolide-1: 4). Fragrances also include esters- and essential oils derived from floral materials and fruits, citrus oils, pure aldehydes, resinoids, notes of musk and other animals (for example, natural isolates of civet, castoreum and musk), balsams, etc. and alcohols (such as, for example, dimyrcetol, phenylethyl alcohol and tetrahydromuguol). Examples of these components useful in the fragrances herein include decyl aldehyde, undecyl aldehyde, undecylenic aldehyde, lauric aldehyde, amyl cinnamic aldehyde, methyl ethyl glycidate glycide, nonyl methyl acetaldehyde, myristic aldehyde, nonalactone, nonyl aldehyde, aldehyde octyl, undecalactone, -hexyl cinnamic aldehyde, benza-Tdehyde, vanillin, heliotrobin, camphor, para-hydroxy phenolbutylone, tetrahydronaphthalene of 6-acetyl 1,1,3,4,4,6-hexamethyl, alpha-methyl ionone, ionone. of gamma-methyl, and amyl-cyclohexanone / and mixtures of these components ^. Other suitable fragrances are those which mask or help to mask the odors associated with perspiration (hereinafter referred to as odor masking fragrances) or odors associated with the inherent malodor of some gel deodorant compositions or the materials of the odors. same. Some non-limiting examples of suitable odor-forming odor fragrances ----- are described in U.S. Patent 5,554,588, U.S. Patent 4,278,658, U.S. Patent 5,501,805, and EP Patent Application 684 037 Al, whose descriptions are incorporated herein by reference. Preferred odor masking fragrances are those that have a value
Deodorant of at least about 0.25, most preferably from about 0.25 to about 3.5, still more preferably from about 0.9 to about 3.5, as measured by the Deodorant Value Test, described in the patent application EP 684 037 Al. Fragrance for use herein may also contain solubilizers, diluents or solvents that are well known in the art. These materials are described in Arctander, Perfume and Flavor Chemicals (Aroma Chemicals), Vol. I and II (1969). These materials typically include dipropylene glycol, diethylene glycol, C6-C6 alcohols, and benzyl alcohol. ~~
GELIFICANT The gel deodorant composition of the present invention comprises a suitable gelling agent to provide the desired strength and application characteristics to the composition. The gelling concentrations vary from about 0.01% to about 20%, preferably from about 0.1% to about 10%, more preferably from about 1% to about 8%, still more preferably from about 3% to about 7%, in weight of the gel deodorant composition. Any known gelling agent or gelling system can be used in the gel deodorant composition of the present invention with the proviso that the selected gelling agents can be melted and form a solution or other homogeneous liquid or liquid dispersion with the selected solvent system described in present at a processing temperature of from about 50 ° C to about 150 ° C, preferably from about 50 ° C to about 120 ° C, more preferably from about 60 ° C to about 100 ° C. The selected gellant > it must also provide the gel deodorant composition with the desired gel matrix after the formulation and at the end of processing which then gives the composition the strength or spreading characteristics. Preferred gelling agents for use in the gel deodorant composition of the present invention are salts of fatty acids, wherein the fatty acid portion has from about 12 to about 40 carbon atoms, preferably from about 12 to about 22 carbon atoms. carbon, more preferably from about 16 to about 20 carbon atoms, still of higher preference of about 18. Carbon atoms suitable for use with these gelling agents include metal salts such as alkali metals, for example, of sodium and potassium, and alkaline earth metals, for example magnesium and aluminum, sodium and potassium salts are preferred, more preferably sodium stearate, sodium palmitate, sodium laurate, sodium arachidate, sodium behenate, potassium stearate, potassium palmitate, sodium myristate, potassium palmitate, aluminum monoedate, and combinations thereof. The most preferred is sodium stearate. Non-limiting examples of fatty acids suitable for producing the fatty acid gelling agents include acids, such as, for example, myristic, palmitic, stearic, oleic, behenic, arachidonic, lauric, linoleic, linolenic, margaric and combinations thereof. These fatty acids are preferably derived from sources, such as, for example, coconut oil, beef tallow, lanolin, fish oil, beeswax, palm oil, peanut oil, olive oil, cottonseed oil. , soybean oil, corn oil, rape seed oil, rosin acids, fats and other natural sources, or are derived by synthetic or semi-synthetic methods well known to those skilled in the art of formulation. Other gelling agents suitable for use in the gel deodorant composition include hydroxy acids, fatty acids, fatty acid esters and amides and fatty acid salts, hydroxy fatty acids, spherical materials, lanolinol materials, and others --- amide gelling agents known to be used as gelling agents or which are otherwise described in detail hereinafter. Non-limiting examples of suitable fatty acid gelling agents include fatty acid and hydroxy acids or alpha hydroxy fatty acids, having from about 10 to about 40 carbon atoms, examples of which include 12-hydroxystearic acid, 12-hydroxylauric acid, 16-hydroxyhexadecanoic acid , behenic acid, euricic acid, stearic acid, caprylic acid, lauric acid, isostearic acid, combinations thereof, and comes out of them. Other non-limiting examples of specific gelling agents suitable for use in the gel deodorant composition include those corresponding to the following formula:
wherein Rx is 0R2 or NR2R3; and R2 and R3 are hydrogen, or an alkyl, aryl, or aplakyl radical that is linear branched or cyclic and has from about 1 to about 22 carbon atoms; preferably from about 1 to about 18 carbon atoms. R2 and R3 may be either the same or different; however, preferably, at least one is a hydrogen atom. Preferred among these gelling agents are those selected from the group consisting of 12-hydroxystearic acid, 12-hydroxystearic acid methyl ester, 12-hydroxystearic acid ethyl ester, 12-hydroxystearic acid benzyl ester of 12-hydroxystearic acid, amide 12-Hydroxies teárico acid, isopropyl amide 12-hydroxies teárico, butylamide 12-hydroxystearic acid, benzylamide 12-hydroxies teárico, phenylamide 12-hydroxies teárico acid, t-butilamida 12-hydroxystearic acid, cyclohexylamide 12-hydroxystearic acid, 1-adamant 12-hydroxystearic acid ilamide, 2-adamant 12-hydroxystearic acid ilamide, 12-hydroxystearic acid diisopropylamide, and mixtures thereof. Non-limiting examples of amide gelling agents suitable for use in the gel deodorant composition include disubstituted or branched monoamide gelling agents, timed or branched monosus monosus gelling agents, triamide gelling agents, and combinations thereof. Preferred are the alkyl amides of the di- and / or tri-basic carboxylic acids or anhydrides which are in accordance with the formula:
i, 9 ?? i - C C N
-X AND Z
C -C -] 11 10
where a structure is formed from the bond of C, C "and X and where" a) Ri is zero, hydroxy, hydrogen, aryl, siloxane or C? -C22 alkyl, C? -C22 alkenyl, alkoxy of C? ~ C22, alkyl C? ~ C22, straight chain, branched or cyclic C, -C22 alkyl ethers, substituted or unsubstituted, saturated or unsaturated, or aryl substituted with C? -C22 alkyl, preferably C 4 -C 8 alkyl, C 4 -C 18 alkenyl, C 4 -C 8 alkoxy, C 4 -C 8 alkyl esters, C 4 -C 8 alkyl ethers, or C 4 -C 18 alkyl substituted aryl, higher preferably C 2 -C 8 alkyl, C 12 -C 18 alkenyl, C 2 -C 8 alkoxy, C 2 -C 8 alkylaryl, C 2 -C 8 alkylethers, or substituted aryl with C 2 -C 18 alkyl; b) R 2, R 4, R 5 and Re are independently or together, hydrogen, hydroxy, aryl, siloxane or C 1 -C 22 alkyl, C 1 -C 22 alkenyl, C 1 -C 22 alkoxy, C 1 -C 22 alkylets , C 1 -C 22 alkylethers, straight chain, branched or cyclic substituted or unsubstituted, saturated or unsaturated, or aryl substituted with C 1 -C 22 alkyl, preferably C 4 -C 6 alkyl, C 4 -C 10 alkenyl, alkoxy of C4-C10, C4-C10 alkyls, C4-C10 alkyl ethers, or aryl substituted with C4-C10 alkyl, more preferably C4-C8 alkyl, C4-C8 alkenyl, C4-C8 alkoxy, alkyl esters of C4-C8, C4-C8 alkyl ethers, or aryl substituted with C4-C8 alkyl; c) R3 is null, hydroxy, hydrogen, C1-C4 alkyl, alkenyl of JJ1-C, C1-C4 alkoxy, alkydsters of C3-C4 or straight, branched or cyclic C, -C4 alkyl ethers, substituted or unsubstituted, saturated or unsaturated, preferably a C 1 -C 4 alkoxy, hydroxy or hydrogen, more preferably a hydroxy or hydrogen;
d) R and Rs are independently or jointly, null, hydrogen, hydroxy, aryl, siloxane or C?-C22 alquilo alkyl, C al-C22 al alkenyl, C?-C22 alco alkoxy, C?-C22 alqu alkylesters, C1-C22 straight chain, branched or cyclic, substituted or unsubstituted, saturated or unsaturated, or aryl substituted with C? -C22 alkyl, preferably C4-1C10 alkyl, C4-C10 alkenyl, C4-C10 alkoxy , C4-C10 alkyl esters, C4-C10 alkyl ethers, or aryl substituted with C4-C10 alkyl, of higher preference C4-C8 alkyl, C4-C8 alkenyl, C4-C8 alkoxy, C-alkyl esters C8, alkylethers of 04 ^ 3, ° aryl substituted with C4-C8 alkyl; e) R9 is zero or hydrogen; f) R6 and R11 are independently or jointly, null, hydrogen, hydroxy, aryl, siloxane or C6-C6 alkyl, C6-C6 alkenyl, C6-C6 alkoxy, C6-C6 alkylesters , straight, branched or cyclic C 1 -C 6 alkylethers, substituted or unsubstituted, saturated or unsaturated, or aryl substituted with C 1 -C 6 alkyl, preferably C 1 -C 4 alkyl, C 1 -C 4 alkenyl, alkoxy of C 1 -C 4, C 1 -C 4 alkylesters, C 1 -C 4 alkylethers, aryl substituted with C 1 -C 4 alkyl or hydrogen, more preferably a hydrogen;
~ g) X is zero, nitrogen, aryl or -f-CH2 -) - n where n is an integer from 1 to 6, preferably - .H2-H1 where n is an integer from 1 to 3; h) Y is zero, acyl or carbonyl; i) Z is zero, hydrogen, hydroxy, aryl, siloxane, nitrogen or C 1 -C 22 alkyl. C 1 -C 22 alkenyl, C 1 -C 22 alkoxy, C 1 -C 22 alkylesters, C, -C 22 straight chain, branched or cyclic alkyl ethers, substituted or unsubstituted, saturated or unsaturated, or aryl substituted with C alkyl? -C22, preferably C4-C10 alkyl, C4-C10 alkenyl, C4-C10 alkoxy, C4-C10 alkyl esters, C4-C10 alkyl ethers, or aryl substituted with C4-C10 alkyl, more preferably C4-C10 alkyl; C4-C8, C4-C8 alkenyl, C4-C8 alkoxy, C4-C8 alkylester, C-C8 alkyl ether, or aryl substituted with C4-C8 alkyl; and j) "a" is a double or single bond with the proviso that: (i) when X is zero, Y, Z, R3, R and R8 are zero, C1 is directly connected to C "and Ri is not hydrogen (ii) when X and Z are not null and Y is zero, X is directly linked to Z, (iii) when Z is zero, a hydrogen or a hydroxy, R7 and R8 are zero, and ~ (iv) when " to "be a double bond, R3 and Rg are null, non-limiting examples of specific alkyl amide gelling agents suitable for use in the gel deodorant composition include alkyl amides of citric acid, ticarbicarbal acid, aconitic acid, nitrilotriacetic acid , succinic acid and itaconic acid, such as, for example, 1,2,3-propane tributyl amide, 2-hydroxy-l, 2,3-propane tributyl amide, 1-propene-1,2,3-trioctylamide, N, N ', N "-tri (acetodecylamide) amine, 2-dodecyl-N, N'-dihexylsuccinamide, and 2-dodecyl-N, I dibutyl succinamide.
POLYMERIC ALCOHOLS The deodorant gel composition of the present invention comprises a polymeric alcohol in combination with a non-polymeric alcohol to solubilize the selected gellant for use in the gel deodorant composition. The solvent combination can also be used to -solubilize the active deodorant or fragrance. The concentration of the polymeric alcohol in the gel deodorant composition ranges from about 5% to about 90%, preferably from about 5% to about 80%, more preferably from about 10% to about 75%, still more preferably about 20% to about 60% by weight of the composition. The term "polymeric alcohol", in the sense in which it is used herein, means any alkoxylated alcohol that is liquid under ambient conditions and that has at least one free hydroxyl group, wherein the polymeric alcohol has from about 1 to about 80, preferably from about 3 to about 20, "repeating alkylene oxide radicals, and wherein each of the repeating alkylene oxide radicals has from 2 to 6 carbon atoms." Non-limiting examples of suitable polymeric alcohols for use in the gel deodorizing composition include diethylene glycol, triethylene glycol, dipropylene glycol, tripropylene glycol, copolymers of polypropylene polyethylene glycol, tet rapropylene glycol, tetraethylene glycol, dibutyl glycol, trimethylenglycol, diethylene glycol monoethyl ether, PEG-8, 1,3-butanediol, 1,4-butanediol, glycerol propoxylate and mixtures thereof Polymeric alcohols Preferred include dipropylene glycol, t-ripropylene glycol, tetrapropylene glycol and mixtures thereof. - As used herein, polyethylene glycol polyethylene glycols, polypropylene glycols and copolymers include alkyl ether derivatives of these compounds (for example, ethyl, propyl, mipstyl and butyl ether derivatives) with the proviso that all of these derivatives have at least one free hydroxyl group. Examples of these compounds are myristyl ether derivatives of polypropylene glycol, such as, for example, PPG-3 mips t ilét er.
NON-POLYMERIC ALCOHOL The gel deodorant composition of the present invention comprises a non-polymeric alcohol as a solvent for the selected gelling agent or gelling system and for use in combination with the polymeric alcohol solvent described herein. The concentrations of non-polymeric alcohol vary from about 5% to about 90%, preferably from about 5% to about 80%, most preferably from about 10% to about 75%, even more preferably from about 20% to about 60% by weight of the composition. - The gel deodorant composition comprises a non-polymeric alcohol as defined herein, wherein the weight ratio of the polymeric to non-polymeric alcohol in the composition ranges from about 18: 1 to about 1: 5, most preferably about 7.5: 1 to about 1: 5, still more preferably from about 4: 1 to about 1: 2. - The polymeric alcohols suitable for use herein are those containing at least two free hydroxyl groups, for example, dihydric and polyhydric and having from about 4 to about 20 carbon atoms, preferably from about 4 to about 10 carbon atoms. carbon, non-limiting examples of which _ include propylene glycol, hexylene glycol, 1,2-hexanediol, 1,3-butylene glycol, 1,2,6-trihydroxyhexane, 1,2,3-t-hydroxyhexane and combinations thereof. Most preferred are hexylene glycol, 1,2-hexanediol or combinations thereof, more preferably 1,2-hexanediol.
The gel deodorizing compositions may further comprise other, additional, polar or other solvents, some non-limiting examples thereof being described in U.S. Patent 5,429,816; Cosmetics, Science, and Technology, Vol. 1, 27-104, edited by Balsam and Sagarin (1972); U.S. Patent 4,202,879; and U.S. Patent 4,816,261, the disclosures of which are incorporated herein by reference.Preferably, the gel deodorant compositions of the present invention are virtually free of propylene glycol, dipropylene glycol, or combinations thereof. the term "practically free" means that preferably the compositions contain less than 20%, more preferably less than 10%, still more preferably zero percent by weight of propylene glycol, dipropylene glycol or combinations thereof.
WATER The gel deodorant compositions of the present invention are aqueous systems comprising from about 0.01% to about 89%, preferably from about 5% to about 50%, most preferably from about 10% to about 30% water by weight of the composition.
GLICERJNA ~ The gel deodorant compositions of the present invention preferably further comprise glycerin at concentrations from zero percent to "about 10 ---%, preferably from about 0.5% to about 7%, still more preferably about 1% to about 6% by weight of the composition.
. OPTIONAL INGREDIENTS The gel deodorant compositions of the present invention may further comprise one or more optional components that may modify the physical, chemical, cosmetic or aesthetic characteristics of the compositions or may serve as additional "active" components when deposited on the skin. The compositions may also comprise optional inert ingredients. Many of these optional ingredients are known for use in deodorants or other personal care compositions and can also be used in the gel deodorant compositions herein, provided that these optional materials are compatible with the essential materials described in present, or otherwise do not unduly damage the performance of the product.Non-limiting examples of optional ingredients suitable for use in the gel deodorant composition herein include pH regulating agents.; additional emollients; humectants; appeasing agents; dyes and pigments; medications, conservatives; and soothing agents such as, for example, aloe vera, allantoin, D-panthenol, avocado oil and other vegetable oils, and lichen extract.
MANUFACTURING METHOD The gel deodorant compositions of the present invention can be made by any of the methods known in the art for the formulation of the deodorant gel compositions. As will be apparent to those skilled in the art, the particular method will depend on the selection of the specific types and amounts of the components employed. In general, the compositions of the present invention can be prepared by mixing the polymeric alcohol, non-polymeric alcohol and deodorant active. The gellant is added with stirring and the mixture is heated to a temperature from about 75 ° C to about 100 ° C to allow the gellant to melt and form a virtually clear or translucent liquid. The resulting liquid is cooled before the fragrance is added (if applicable), and then the cooled composition is emptied into an appropriate container or dispenser at about 70 ° C and allowed to solidify inside the container or distributor for cooling or allow it to cool. cool the contained composition at room temperature.
METHOD OF USE The gel deodorant composition of the present invention can be "applied topically to the skin by any known or otherwise effective method to control the bad, odor associated with perspiration." These methods comprise applying to the armpit or other area. of the human skin a safe and effective amount of the gel deodorant composition of the present invention In this context, the term "safe and effective amount" means an amount of the gel deodorant composition applied topically to the skin which is effective to mask, reduce --- or eliminate the bad odor associated with human perspiration as long as it is safe for human use at a reasonable risk / benefit ratio.In this context, a safe and effective amount typically varies from approximately 0.1 grams per armpit at approximately 2.0 grams per armpit The compositions are preferably applied to the armpit or other area of the skin once or twice a day, preferably once a day.
EXAMPLES The following examples illustrate specific embodiments of the gel deodorant compositions of the present invention, including methods of manufacture and use, although not intended to be limiting thereof. Other modifications may be attempted by the skilled artisan without departing from the spirit and scope of this invention. All compositions provide improved application aesthetics and / or low irritation performance. Gel deodorant compositions containing 1,2-hexanediql have improved visual clarity, and compositions containing the riclosan / triclocarban combination provide improved deodorant efficacy. Each of the exemplified compositions are prepared by combining all the components listed, except for the gellant and the fragrance where applicable, and heating with agitation the combination of the ingredients at a temperature above the melting point of the gellant but less than 1 í 0 ° C. The gelling agent is then added while continuing the heating and stirring of the mixture until it results in a clear single phase solution, at which point the mixture is cooled to a temperature of between 69 ° C and 80 ° C. . The fragrance is added with agitation to the cooled mixture. The mixture containing the fragrance is then emptied into an appropriate distributor or other container and allowed to solidify by cooling to room temperature.
The compositions described in Examples I-VI were also formulated with 0.25% triclocarban instead of 0.3% triclosan. Approximately 0.05% by weight of water was also added to the triclocarbano formulations.
Claims (10)
- CLAIMS: 1. A deodorant gel composition characterized in that it comprises: (a) from 0.001% to 50% by weight of a deodorant active, fragrance, or combination thereof; (b) from 0.01% to 20% by weight of a gelling agent; (c) from 5% to 90% "by weight of a polymeric alcohol having at least one free hydroxyl group and also having from 2 to 80 alkoxylated radicals each having 2 to 6 carbon atoms; ~~ (d) 5% to 90% by weight of a non-polymeric alcohol having at least two free hydroxyl groups and from 4 to 20 carbon atoms, wherein the weight ratio of the polymeric to non-polymeric alcohol is from 18: 1 to 1: 5 (e) from 0% to 10% by weight of glycerin, and r- (f) from 0.01% to 89% by weight of water.
- 2. The composition, according to claim 1, characterized in that the gelling agent is a fatty acid salt having 12 to 22 carbon atoms.
- 3. The composition, according to claim 2, characterized in that the fatty acid salt is selected from the group consisting of sodium stearate, sodium palmitate, sodium myristate, sodium laurate, sodium behenate, sodium arachidate. potassium stearate, potassium palmitate, potassium myristate and mixtures thereof.
- 4. The composition, according to claim 3, characterized in that the fatty acid salt comprises sodium stearate.
- 5. The composition, according to any of the preceding claims, characterized in that the - polymeric alcohol is selected from the group consisting of diethylene glycol, triethylene glycol, dipropylene glycol, tripropylene glycol, polypropylene polyethylene glycol copolymers, tetrapropylene glycol, tetraethylene glycol, dibutylene glycol, trimethylene glycol, diethylene glycol monoethyl ether. , PEG-8, glycerol propoxylate and mixtures thereof.
- 6. The composition, according to claim 5, characterized in that the composition comprises a mixture of two or more polymeric alcohols selected from the group consisting of diethylene glycol, triethylene glycol, dipropylene glycol, tripropylene glycol, polypropylene polyethylene glycol copolymers, tetrapropylene glycol, tetraethylene glycol, dibutylene glycol, trimethylene glycol. , monoethylether ------ of diethylene glycol, PEG-8, and glycerol propoxylate.
- 7. The composition, according to any of the preceding claims, characterized in that the deodorant active is selected from the group consisting of triclocarban, triclosan and combinations thereof.
- ~ Q The composition, according to claim 7, characterized in that the composition comprises from 0.01% to 1.0% by weight of triclosan and from 0.01% to 1.0% by weight of triclocarban.
- 9. The composition, in accordance with which it was of the preceding claims, characterized in that the non-polymeric alcohol is selected from the group consisting of hexylene glycol, 1,2-hexanediol and combinations thereof.
- 10. The composition, according to any one of the preceding claims, characterized in that the composition comprises from about 1% to about 7% by weight of glycerin. SUMMARY OF THE INVENTION Gel deodorizing compositions are described comprising (a) from about 0.001% to about 50% by weight of a deodorant active, fragrance, or combination thereof; (b) from about 0.01% to about 20% by weight of a gellant; (c) from about 5% to about 90% by weight of a polymeric alcohol having at least one free hydroxyl group and also having from about 2 to about 80 alkoxylated radicals, wherein the alkoxylated radical contains from about 2 to about 6 carbon atoms; (d) from about 5% to about 90% by weight of a non-polymeric alcohol having at least two free hydroxyl groups and also having from about 4 to about 20 carbon atoms, wherein the weight ratio of the polymeric alcohol to Non-polymeric alcohol is from about 18: 1 to about 1: 5; (e) from zero percent to about 10% by weight of glycerin; and (f) from about 0.01% to about 89% by weight of water. A method for controlling odor associated with perspiration is also described by topical application of any deodorant composition containing a select combination of triclosan and triclocarban. All of these compositions remain clear or translucent for long periods of time and provide minimal or no irritation to the skin in addition to improved cosmetic benefits such as for example dry sensation, ease of application, emolliency, fragrance durability and / or no dusty residue.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US08/880,935 | 1998-05-01 | ||
US09071100 | 1998-05-01 |
Publications (1)
Publication Number | Publication Date |
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MXPA99011743A true MXPA99011743A (en) | 2000-06-01 |
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