EP3274055A1 - Cosmetic preparations with low textile adhesion - Google Patents
Cosmetic preparations with low textile adhesionInfo
- Publication number
- EP3274055A1 EP3274055A1 EP16707465.7A EP16707465A EP3274055A1 EP 3274055 A1 EP3274055 A1 EP 3274055A1 EP 16707465 A EP16707465 A EP 16707465A EP 3274055 A1 EP3274055 A1 EP 3274055A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- acid
- weight
- ethylhexyl
- antiperspirant
- esters
- 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.)
- Withdrawn
Links
- 239000002537 cosmetic Substances 0.000 title claims abstract description 59
- 239000004753 textile Substances 0.000 title claims abstract description 38
- 238000002360 preparation method Methods 0.000 title description 4
- 239000000203 mixture Substances 0.000 claims abstract description 164
- 230000001166 anti-perspirative effect Effects 0.000 claims abstract description 64
- 239000003213 antiperspirant Substances 0.000 claims abstract description 64
- 150000002148 esters Chemical class 0.000 claims abstract description 59
- -1 polydimethylsiloxane Polymers 0.000 claims abstract description 50
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 claims abstract description 36
- 239000004205 dimethyl polysiloxane Substances 0.000 claims abstract description 26
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 14
- 125000004122 cyclic group Chemical group 0.000 claims abstract description 14
- 229920006395 saturated elastomer Polymers 0.000 claims abstract description 13
- ACIAHEMYLLBZOI-ZZXKWVIFSA-N Unsaturated alcohol Chemical compound CC\C(CO)=C/C ACIAHEMYLLBZOI-ZZXKWVIFSA-N 0.000 claims abstract description 6
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims abstract description 6
- 150000003627 tricarboxylic acid derivatives Chemical class 0.000 claims abstract description 6
- 230000002829 reductive effect Effects 0.000 claims abstract description 3
- 235000013870 dimethyl polysiloxane Nutrition 0.000 claims description 34
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 claims description 30
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 claims description 24
- 239000004480 active ingredient Substances 0.000 claims description 15
- OSCJHTSDLYVCQC-UHFFFAOYSA-N 2-ethylhexyl 4-[[4-[4-(tert-butylcarbamoyl)anilino]-6-[4-(2-ethylhexoxycarbonyl)anilino]-1,3,5-triazin-2-yl]amino]benzoate Chemical compound C1=CC(C(=O)OCC(CC)CCCC)=CC=C1NC1=NC(NC=2C=CC(=CC=2)C(=O)NC(C)(C)C)=NC(NC=2C=CC(=CC=2)C(=O)OCC(CC)CCCC)=N1 OSCJHTSDLYVCQC-UHFFFAOYSA-N 0.000 claims description 14
- AZDRQVAHHNSJOQ-UHFFFAOYSA-N alumane Chemical class [AlH3] AZDRQVAHHNSJOQ-UHFFFAOYSA-N 0.000 claims description 14
- SFAAOBGYWOUHLU-UHFFFAOYSA-N 2-ethylhexyl hexadecanoate Chemical compound CCCCCCCCCCCCCCCC(=O)OCC(CC)CCCC SFAAOBGYWOUHLU-UHFFFAOYSA-N 0.000 claims description 13
- HIQIXEFWDLTDED-UHFFFAOYSA-N 4-hydroxy-1-piperidin-4-ylpyrrolidin-2-one Chemical compound O=C1CC(O)CN1C1CCNCC1 HIQIXEFWDLTDED-UHFFFAOYSA-N 0.000 claims description 13
- XMSXQFUHVRWGNA-UHFFFAOYSA-N Decamethylcyclopentasiloxane Chemical compound C[Si]1(C)O[Si](C)(C)O[Si](C)(C)O[Si](C)(C)O[Si](C)(C)O1 XMSXQFUHVRWGNA-UHFFFAOYSA-N 0.000 claims description 13
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims description 13
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 claims description 12
- 239000000443 aerosol Substances 0.000 claims description 12
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 claims description 12
- AEMRFAOFKBGASW-UHFFFAOYSA-N Glycolic acid Chemical compound OCC(O)=O AEMRFAOFKBGASW-UHFFFAOYSA-N 0.000 claims description 10
- 235000015165 citric acid Nutrition 0.000 claims description 10
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 10
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 claims description 8
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 claims description 8
- DOOTYTYQINUNNV-UHFFFAOYSA-N Triethyl citrate Chemical compound CCOC(=O)CC(O)(C(=O)OCC)CC(=O)OCC DOOTYTYQINUNNV-UHFFFAOYSA-N 0.000 claims description 8
- 235000006408 oxalic acid Nutrition 0.000 claims description 8
- 239000011975 tartaric acid Substances 0.000 claims description 8
- 235000002906 tartaric acid Nutrition 0.000 claims description 8
- 239000001069 triethyl citrate Substances 0.000 claims description 8
- VMYFZRTXGLUXMZ-UHFFFAOYSA-N triethyl citrate Natural products CCOC(=O)C(O)(C(=O)OCC)C(=O)OCC VMYFZRTXGLUXMZ-UHFFFAOYSA-N 0.000 claims description 8
- 235000013769 triethyl citrate Nutrition 0.000 claims description 8
- LWLRMRFJCCMNML-UHFFFAOYSA-N 2-ethylhexyl dodecanoate Chemical compound CCCCCCCCCCCC(=O)OCC(CC)CCCC LWLRMRFJCCMNML-UHFFFAOYSA-N 0.000 claims description 6
- OPJWPPVYCOPDCM-UHFFFAOYSA-N 2-ethylhexyl octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(CC)CCCC OPJWPPVYCOPDCM-UHFFFAOYSA-N 0.000 claims description 6
- GRXOKLJPWSYWIA-UHFFFAOYSA-N 2-ethylhexyl tetradecanoate Chemical compound CCCCCCCCCCCCCC(=O)OCC(CC)CCCC GRXOKLJPWSYWIA-UHFFFAOYSA-N 0.000 claims description 6
- KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 claims description 6
- 239000001361 adipic acid Substances 0.000 claims description 6
- 235000011037 adipic acid Nutrition 0.000 claims description 6
- KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 claims description 6
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 6
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 6
- XUGNVMKQXJXZCD-UHFFFAOYSA-N isopropyl palmitate Chemical compound CCCCCCCCCCCCCCCC(=O)OC(C)C XUGNVMKQXJXZCD-UHFFFAOYSA-N 0.000 claims description 6
- 239000004310 lactic acid Substances 0.000 claims description 6
- 235000014655 lactic acid Nutrition 0.000 claims description 6
- QAOJADINKLMTRR-UHFFFAOYSA-N octan-3-yl 16-methylheptadecanoate Chemical compound CCCCCC(CC)OC(=O)CCCCCCCCCCCCCCC(C)C QAOJADINKLMTRR-UHFFFAOYSA-N 0.000 claims description 6
- 230000007480 spreading Effects 0.000 claims description 6
- BJEPYKJPYRNKOW-REOHCLBHSA-N (S)-malic acid Chemical compound OC(=O)[C@@H](O)CC(O)=O BJEPYKJPYRNKOW-REOHCLBHSA-N 0.000 claims description 5
- RTBFRGCFXZNCOE-UHFFFAOYSA-N 1-methylsulfonylpiperidin-4-one Chemical compound CS(=O)(=O)N1CCC(=O)CC1 RTBFRGCFXZNCOE-UHFFFAOYSA-N 0.000 claims description 5
- TWEZFVUFZGJVTF-UHFFFAOYSA-N 11-methyldodecyl nonanoate Chemical compound CCCCCCCCC(=O)OCCCCCCCCCCC(C)C TWEZFVUFZGJVTF-UHFFFAOYSA-N 0.000 claims description 5
- KMUBFTBPGVULKC-UHFFFAOYSA-N 2-hexyldecyl dodecanoate Chemical compound CCCCCCCCCCCC(=O)OCC(CCCCCC)CCCCCCCC KMUBFTBPGVULKC-UHFFFAOYSA-N 0.000 claims description 5
- MWKPHOIHTLQZIY-UHFFFAOYSA-N 2-hexyldecyl octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(CCCCCC)CCCCCCCC MWKPHOIHTLQZIY-UHFFFAOYSA-N 0.000 claims description 5
- RUDXBXPTJPNTSO-UHFFFAOYSA-N 2-octyldodecyl hexadecanoate Chemical compound CCCCCCCCCCCCCCCC(=O)OCC(CCCCCCCC)CCCCCCCCCC RUDXBXPTJPNTSO-UHFFFAOYSA-N 0.000 claims description 5
- UIVPNOBLHXUKDX-UHFFFAOYSA-N 3,5,5-trimethylhexyl 3,5,5-trimethylhexanoate Chemical compound CC(C)(C)CC(C)CCOC(=O)CC(C)CC(C)(C)C UIVPNOBLHXUKDX-UHFFFAOYSA-N 0.000 claims description 5
- SJIDAAGFCNIAJP-UHFFFAOYSA-N 6-methylheptyl octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCCCCCC(C)C SJIDAAGFCNIAJP-UHFFFAOYSA-N 0.000 claims description 5
- XUVVLJKRLAXOKZ-UHFFFAOYSA-N 7-methyloctyl octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCCCCCCC(C)C XUVVLJKRLAXOKZ-UHFFFAOYSA-N 0.000 claims description 5
- BJEPYKJPYRNKOW-UHFFFAOYSA-N alpha-hydroxysuccinic acid Natural products OC(=O)C(O)CC(O)=O BJEPYKJPYRNKOW-UHFFFAOYSA-N 0.000 claims description 5
- JFCQEDHGNNZCLN-UHFFFAOYSA-N anhydrous glutaric acid Natural products OC(=O)CCCC(O)=O JFCQEDHGNNZCLN-UHFFFAOYSA-N 0.000 claims description 5
- 229940071160 cocoate Drugs 0.000 claims description 5
- HTDJPCNNEPUOOQ-UHFFFAOYSA-N hexamethylcyclotrisiloxane Chemical compound C[Si]1(C)O[Si](C)(C)O[Si](C)(C)O1 HTDJPCNNEPUOOQ-UHFFFAOYSA-N 0.000 claims description 5
- 229940090854 hexyldecyl laurate Drugs 0.000 claims description 5
- 229940100554 isononyl isononanoate Drugs 0.000 claims description 5
- 229940089456 isopropyl stearate Drugs 0.000 claims description 5
- 239000001630 malic acid Substances 0.000 claims description 5
- 235000011090 malic acid Nutrition 0.000 claims description 5
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 5
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 5
- HMMGMWAXVFQUOA-UHFFFAOYSA-N octamethylcyclotetrasiloxane Chemical compound C[Si]1(C)O[Si](C)(C)O[Si](C)(C)O[Si](C)(C)O1 HMMGMWAXVFQUOA-UHFFFAOYSA-N 0.000 claims description 5
- ZPWFUIUNWDIYCJ-UHFFFAOYSA-N propan-2-yl octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OC(C)C ZPWFUIUNWDIYCJ-UHFFFAOYSA-N 0.000 claims description 5
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 5
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 5
- 229940008099 dimethicone Drugs 0.000 claims description 4
- 125000004494 ethyl ester group Chemical group 0.000 claims description 4
- IUMSDRXLFWAGNT-UHFFFAOYSA-N Dodecamethylcyclohexasiloxane Chemical compound C[Si]1(C)O[Si](C)(C)O[Si](C)(C)O[Si](C)(C)O[Si](C)(C)O[Si](C)(C)O1 IUMSDRXLFWAGNT-UHFFFAOYSA-N 0.000 claims description 3
- LGEZTMRIZWCDLW-UHFFFAOYSA-N 14-methylpentadecyl octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCCCCCCCCCCCCCC(C)C LGEZTMRIZWCDLW-UHFFFAOYSA-N 0.000 claims description 2
- 229940078545 isocetyl stearate Drugs 0.000 claims description 2
- 240000007817 Olea europaea Species 0.000 claims 1
- 229910052799 carbon Inorganic materials 0.000 claims 1
- 239000003795 chemical substances by application Substances 0.000 abstract description 7
- 239000002253 acid Substances 0.000 abstract description 3
- 239000003921 oil Substances 0.000 description 68
- 235000019198 oils Nutrition 0.000 description 68
- 239000003205 fragrance Substances 0.000 description 14
- 239000002304 perfume Substances 0.000 description 14
- 239000000047 product Substances 0.000 description 11
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 11
- 229910052782 aluminium Inorganic materials 0.000 description 8
- 239000007788 liquid Substances 0.000 description 8
- 230000015572 biosynthetic process Effects 0.000 description 7
- 238000005538 encapsulation Methods 0.000 description 7
- 239000000463 material Substances 0.000 description 7
- 239000013543 active substance Substances 0.000 description 6
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical class [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 6
- 230000001877 deodorizing effect Effects 0.000 description 6
- LVYZJEPLMYTTGH-UHFFFAOYSA-H dialuminum chloride pentahydroxide dihydrate Chemical compound [Cl-].[Al+3].[OH-].[OH-].[Al+3].[OH-].[OH-].[OH-].O.O LVYZJEPLMYTTGH-UHFFFAOYSA-H 0.000 description 6
- 239000000126 substance Substances 0.000 description 6
- 239000006096 absorbing agent Substances 0.000 description 5
- 239000002775 capsule Substances 0.000 description 5
- 150000001875 compounds Chemical class 0.000 description 5
- 230000002401 inhibitory effect Effects 0.000 description 5
- 238000000034 method Methods 0.000 description 5
- 229920000742 Cotton Polymers 0.000 description 4
- VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 239000010696 ester oil Substances 0.000 description 4
- MGSRCZKZVOBKFT-UHFFFAOYSA-N thymol Chemical compound CC(C)C1=CC=C(C)C=C1O MGSRCZKZVOBKFT-UHFFFAOYSA-N 0.000 description 4
- 239000000341 volatile oil Substances 0.000 description 4
- 238000005406 washing Methods 0.000 description 4
- DRTBYQJIHFSKDT-UHFFFAOYSA-N 2-methyl-5-phenylpentan-1-ol Chemical compound OCC(C)CCCC1=CC=CC=C1 DRTBYQJIHFSKDT-UHFFFAOYSA-N 0.000 description 3
- QCDWFXQBSFUVSP-UHFFFAOYSA-N 2-phenoxyethanol Chemical compound OCCOC1=CC=CC=C1 QCDWFXQBSFUVSP-UHFFFAOYSA-N 0.000 description 3
- MSHFRERJPWKJFX-UHFFFAOYSA-N 4-Methoxybenzyl alcohol Chemical compound COC1=CC=C(CO)C=C1 MSHFRERJPWKJFX-UHFFFAOYSA-N 0.000 description 3
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
- 239000004354 Hydroxyethyl cellulose Substances 0.000 description 3
- 229920000663 Hydroxyethyl cellulose Polymers 0.000 description 3
- 229920000881 Modified starch Polymers 0.000 description 3
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 3
- 235000010443 alginic acid Nutrition 0.000 description 3
- 229920000615 alginic acid Polymers 0.000 description 3
- 244000052616 bacterial pathogen Species 0.000 description 3
- 229960001716 benzalkonium Drugs 0.000 description 3
- 239000001768 carboxy methyl cellulose Substances 0.000 description 3
- 235000010948 carboxy methyl cellulose Nutrition 0.000 description 3
- 239000008112 carboxymethyl-cellulose Substances 0.000 description 3
- 229920001525 carrageenan Polymers 0.000 description 3
- 235000010418 carrageenan Nutrition 0.000 description 3
- 239000002734 clay mineral Substances 0.000 description 3
- 239000000470 constituent Substances 0.000 description 3
- 239000003599 detergent Substances 0.000 description 3
- 230000002209 hydrophobic effect Effects 0.000 description 3
- 235000019447 hydroxyethyl cellulose Nutrition 0.000 description 3
- 235000019426 modified starch Nutrition 0.000 description 3
- 229960005323 phenoxyethanol Drugs 0.000 description 3
- 239000000419 plant extract Substances 0.000 description 3
- 229920001223 polyethylene glycol Polymers 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- 239000007921 spray Substances 0.000 description 3
- 210000004243 sweat Anatomy 0.000 description 3
- 239000002562 thickening agent Substances 0.000 description 3
- OOCCDEMITAIZTP-QPJJXVBHSA-N (E)-cinnamyl alcohol Chemical compound OC\C=C\C1=CC=CC=C1 OOCCDEMITAIZTP-QPJJXVBHSA-N 0.000 description 2
- CGMOOAUESLSUKM-UHFFFAOYSA-N 2-benzylheptan-1-ol Chemical compound CCCCCC(CO)CC1=CC=CC=C1 CGMOOAUESLSUKM-UHFFFAOYSA-N 0.000 description 2
- WRMNZCZEMHIOCP-UHFFFAOYSA-N 2-phenylethanol Chemical compound OCCC1=CC=CC=C1 WRMNZCZEMHIOCP-UHFFFAOYSA-N 0.000 description 2
- OALYTRUKMRCXNH-UHFFFAOYSA-N 5-pentyloxolan-2-one Chemical compound CCCCCC1CCC(=O)O1 OALYTRUKMRCXNH-UHFFFAOYSA-N 0.000 description 2
- ZCTQGTTXIYCGGC-UHFFFAOYSA-N Benzyl salicylate Chemical compound OC1=CC=CC=C1C(=O)OCC1=CC=CC=C1 ZCTQGTTXIYCGGC-UHFFFAOYSA-N 0.000 description 2
- UYWQUFXKFGHYNT-UHFFFAOYSA-N Benzylformate Chemical compound O=COCC1=CC=CC=C1 UYWQUFXKFGHYNT-UHFFFAOYSA-N 0.000 description 2
- 108090000790 Enzymes Proteins 0.000 description 2
- 102000004190 Enzymes Human genes 0.000 description 2
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 2
- YLQBMQCUIZJEEH-UHFFFAOYSA-N Furan Chemical compound C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 2
- GLZPCOQZEFWAFX-UHFFFAOYSA-N Geraniol Chemical compound CC(C)=CCCC(C)=CCO GLZPCOQZEFWAFX-UHFFFAOYSA-N 0.000 description 2
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- 229920002774 Maltodextrin Polymers 0.000 description 2
- 239000002202 Polyethylene glycol Substances 0.000 description 2
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
- 229920002472 Starch Polymers 0.000 description 2
- 240000007313 Tilia cordata Species 0.000 description 2
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical class [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- 150000001299 aldehydes Chemical class 0.000 description 2
- 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 2
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- 235000012216 bentonite Nutrition 0.000 description 2
- CYDRXTMLKJDRQH-UHFFFAOYSA-N benzododecinium Chemical compound CCCCCCCCCCCC[N+](C)(C)CC1=CC=CC=C1 CYDRXTMLKJDRQH-UHFFFAOYSA-N 0.000 description 2
- QUKGYYKBILRGFE-UHFFFAOYSA-N benzyl acetate Chemical compound CC(=O)OCC1=CC=CC=C1 QUKGYYKBILRGFE-UHFFFAOYSA-N 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- NEHNMFOYXAPHSD-UHFFFAOYSA-N citronellal Chemical compound O=CCC(C)CCC=C(C)C NEHNMFOYXAPHSD-UHFFFAOYSA-N 0.000 description 2
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- 239000002781 deodorant agent Substances 0.000 description 2
- KNXDJTLIRRQLBE-UHFFFAOYSA-H dialuminum;propane-1,2-diol;chloride;pentahydroxide;hydrate Chemical compound O.[OH-].[OH-].[OH-].[OH-].[OH-].[Al+3].[Al+3].[Cl-].CC(O)CO KNXDJTLIRRQLBE-UHFFFAOYSA-H 0.000 description 2
- FLKPEMZONWLCSK-UHFFFAOYSA-N diethyl phthalate Chemical compound CCOC(=O)C1=CC=CC=C1C(=O)OCC FLKPEMZONWLCSK-UHFFFAOYSA-N 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 239000003995 emulsifying agent Substances 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- 150000002170 ethers Chemical class 0.000 description 2
- LZCLXQDLBQLTDK-UHFFFAOYSA-N ethyl 2-hydroxypropanoate Chemical compound CCOC(=O)C(C)O LZCLXQDLBQLTDK-UHFFFAOYSA-N 0.000 description 2
- RRAFCDWBNXTKKO-UHFFFAOYSA-N eugenol Chemical compound COC1=CC(CC=C)=CC=C1O RRAFCDWBNXTKKO-UHFFFAOYSA-N 0.000 description 2
- 239000000284 extract Substances 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- BXWNKGSJHAJOGX-UHFFFAOYSA-N hexadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCO BXWNKGSJHAJOGX-UHFFFAOYSA-N 0.000 description 2
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- 150000002430 hydrocarbons Chemical class 0.000 description 2
- 239000001866 hydroxypropyl methyl cellulose Substances 0.000 description 2
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- UFVKGYZPFZQRLF-UHFFFAOYSA-N hydroxypropyl methyl cellulose Chemical compound OC1C(O)C(OC)OC(CO)C1OC1C(O)C(O)C(OC2C(C(O)C(OC3C(C(O)C(O)C(CO)O3)O)C(CO)O2)O)C(CO)O1 UFVKGYZPFZQRLF-UHFFFAOYSA-N 0.000 description 2
- BTFJIXJJCSYFAL-UHFFFAOYSA-N icosan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCCCO BTFJIXJJCSYFAL-UHFFFAOYSA-N 0.000 description 2
- 230000003993 interaction Effects 0.000 description 2
- 150000002576 ketones Chemical class 0.000 description 2
- CDOSHBSSFJOMGT-UHFFFAOYSA-N linalool Chemical compound CC(C)=CCCC(C)(O)C=C CDOSHBSSFJOMGT-UHFFFAOYSA-N 0.000 description 2
- UWKAYLJWKGQEPM-LBPRGKRZSA-N linalyl acetate Chemical compound CC(C)=CCC[C@](C)(C=C)OC(C)=O UWKAYLJWKGQEPM-LBPRGKRZSA-N 0.000 description 2
- VAMXMNNIEUEQDV-UHFFFAOYSA-N methyl anthranilate Chemical compound COC(=O)C1=CC=CC=C1N VAMXMNNIEUEQDV-UHFFFAOYSA-N 0.000 description 2
- 229920000609 methyl cellulose Polymers 0.000 description 2
- 239000001923 methylcellulose Substances 0.000 description 2
- 235000010981 methylcellulose Nutrition 0.000 description 2
- 229910052901 montmorillonite Inorganic materials 0.000 description 2
- GLDOVTGHNKAZLK-UHFFFAOYSA-N octadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCO GLDOVTGHNKAZLK-UHFFFAOYSA-N 0.000 description 2
- 230000003287 optical effect Effects 0.000 description 2
- MDHYEMXUFSJLGV-UHFFFAOYSA-N phenethyl acetate Chemical compound CC(=O)OCCC1=CC=CC=C1 MDHYEMXUFSJLGV-UHFFFAOYSA-N 0.000 description 2
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- 229960001859 domiphen bromide Drugs 0.000 description 1
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- 235000019421 lipase Nutrition 0.000 description 1
- 239000006210 lotion Substances 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- 229940102398 methyl anthranilate Drugs 0.000 description 1
- YLGXILFCIXHCMC-JHGZEJCSSA-N methyl cellulose Chemical compound COC1C(OC)C(OC)C(COC)O[C@H]1O[C@H]1C(OC)C(OC)C(OC)OC1COC YLGXILFCIXHCMC-JHGZEJCSSA-N 0.000 description 1
- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 229940078812 myristyl myristate Drugs 0.000 description 1
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 1
- GOQYKNQRPGWPLP-UHFFFAOYSA-N n-heptadecyl alcohol Natural products CCCCCCCCCCCCCCCCCO GOQYKNQRPGWPLP-UHFFFAOYSA-N 0.000 description 1
- OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 1
- 229910000273 nontronite Inorganic materials 0.000 description 1
- 150000002896 organic halogen compounds Chemical class 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- ADGFKRMKSIAMAI-UHFFFAOYSA-L oxygen(2-);zirconium(4+);chloride;hydroxide Chemical compound [OH-].[O-2].[Cl-].[Zr+4] ADGFKRMKSIAMAI-UHFFFAOYSA-L 0.000 description 1
- RUVINXPYWBROJD-UHFFFAOYSA-N para-methoxyphenyl Natural products COC1=CC=C(C=CC)C=C1 RUVINXPYWBROJD-UHFFFAOYSA-N 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 239000001814 pectin Substances 0.000 description 1
- 229920001277 pectin Polymers 0.000 description 1
- 235000010987 pectin Nutrition 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 229940067107 phenylethyl alcohol Drugs 0.000 description 1
- 229910052615 phyllosilicate Inorganic materials 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920002959 polymer blend Polymers 0.000 description 1
- 229920002689 polyvinyl acetate Polymers 0.000 description 1
- 239000011118 polyvinyl acetate Substances 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 229920006316 polyvinylpyrrolidine Polymers 0.000 description 1
- 230000008092 positive effect Effects 0.000 description 1
- GRLPQNLYRHEGIJ-UHFFFAOYSA-J potassium aluminium sulfate Chemical compound [Al+3].[K+].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O GRLPQNLYRHEGIJ-UHFFFAOYSA-J 0.000 description 1
- 235000013406 prebiotics Nutrition 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- 239000003380 propellant Substances 0.000 description 1
- RUOJZAUFBMNUDX-UHFFFAOYSA-N propylene carbonate Chemical compound CC1COC(=O)O1 RUOJZAUFBMNUDX-UHFFFAOYSA-N 0.000 description 1
- 150000003856 quaternary ammonium compounds Chemical class 0.000 description 1
- 229940032044 quaternium-18 Drugs 0.000 description 1
- 230000002441 reversible effect Effects 0.000 description 1
- 235000019719 rose oil Nutrition 0.000 description 1
- 239000010666 rose oil Substances 0.000 description 1
- 239000010670 sage oil Substances 0.000 description 1
- 229910000275 saponite Inorganic materials 0.000 description 1
- 125000005624 silicic acid group Chemical class 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 239000002884 skin cream Substances 0.000 description 1
- 229910021647 smectite Inorganic materials 0.000 description 1
- 229940087596 sodium phenolsulfonate Drugs 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 229940080313 sodium starch Drugs 0.000 description 1
- BLXAGSNYHSQSRC-UHFFFAOYSA-M sodium;2-hydroxybenzenesulfonate Chemical compound [Na+].OC1=CC=CC=C1S([O-])(=O)=O BLXAGSNYHSQSRC-UHFFFAOYSA-M 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 238000001694 spray drying Methods 0.000 description 1
- 108060007951 sulfatase Proteins 0.000 description 1
- 239000000375 suspending agent Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 235000012222 talc Nutrition 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 150000003505 terpenes Chemical class 0.000 description 1
- 229940116411 terpineol Drugs 0.000 description 1
- DZKXJUASMGQEMA-UHFFFAOYSA-N tetradecyl tetradecanoate Chemical compound CCCCCCCCCCCCCCOC(=O)CCCCCCCCCCCCC DZKXJUASMGQEMA-UHFFFAOYSA-N 0.000 description 1
- 239000010678 thyme oil Substances 0.000 description 1
- 229960000790 thymol Drugs 0.000 description 1
- 239000005028 tinplate Substances 0.000 description 1
- CRDAMVZIKSXKFV-UHFFFAOYSA-N trans-Farnesol Natural products CC(C)=CCCC(C)=CCCC(C)=CCO CRDAMVZIKSXKFV-UHFFFAOYSA-N 0.000 description 1
- BJIOGJUNALELMI-UHFFFAOYSA-N trans-isoeugenol Natural products COC1=CC(C=CC)=CC=C1O BJIOGJUNALELMI-UHFFFAOYSA-N 0.000 description 1
- ICUTUKXCWQYESQ-UHFFFAOYSA-N triclocarban Chemical compound C1=CC(Cl)=CC=C1NC(=O)NC1=CC=C(Cl)C(Cl)=C1 ICUTUKXCWQYESQ-UHFFFAOYSA-N 0.000 description 1
- 229960003500 triclosan Drugs 0.000 description 1
- VXYADVIJALMOEQ-UHFFFAOYSA-K tris(lactato)aluminium Chemical compound CC(O)C(=O)O[Al](OC(=O)C(C)O)OC(=O)C(C)O VXYADVIJALMOEQ-UHFFFAOYSA-K 0.000 description 1
- 229940075466 undecylenate Drugs 0.000 description 1
- 235000021122 unsaturated fatty acids Nutrition 0.000 description 1
- 150000004670 unsaturated fatty acids Chemical class 0.000 description 1
- 239000010679 vetiver oil Substances 0.000 description 1
- 229920001285 xanthan gum Polymers 0.000 description 1
- ZFNVDHOSLNRHNN-UHFFFAOYSA-N xi-3-(4-Isopropylphenyl)-2-methylpropanal Chemical compound O=CC(C)CC1=CC=C(C(C)C)C=C1 ZFNVDHOSLNRHNN-UHFFFAOYSA-N 0.000 description 1
- 238000004383 yellowing Methods 0.000 description 1
- 239000010457 zeolite Substances 0.000 description 1
- 235000005074 zinc chloride Nutrition 0.000 description 1
- 239000011592 zinc chloride Substances 0.000 description 1
- 150000003752 zinc compounds Chemical class 0.000 description 1
- 229940071566 zinc glycinate Drugs 0.000 description 1
- 229940050168 zinc lactate Drugs 0.000 description 1
- 235000000193 zinc lactate Nutrition 0.000 description 1
- 239000011576 zinc lactate Substances 0.000 description 1
- 229940118827 zinc phenolsulfonate Drugs 0.000 description 1
- GAWWVVGZMLGEIW-GNNYBVKZSA-L zinc ricinoleate Chemical compound [Zn+2].CCCCCC[C@@H](O)C\C=C/CCCCCCCC([O-])=O.CCCCCC[C@@H](O)C\C=C/CCCCCCCC([O-])=O GAWWVVGZMLGEIW-GNNYBVKZSA-L 0.000 description 1
- 229940100530 zinc ricinoleate Drugs 0.000 description 1
- NWONKYPBYAMBJT-UHFFFAOYSA-L zinc sulfate Chemical compound [Zn+2].[O-]S([O-])(=O)=O NWONKYPBYAMBJT-UHFFFAOYSA-L 0.000 description 1
- 229910000368 zinc sulfate Inorganic materials 0.000 description 1
- 229960001763 zinc sulfate Drugs 0.000 description 1
- UOXSXMSTSYWNMH-UHFFFAOYSA-L zinc;2-aminoacetate Chemical compound [Zn+2].NCC([O-])=O.NCC([O-])=O UOXSXMSTSYWNMH-UHFFFAOYSA-L 0.000 description 1
- BOVNWDGXGNVNQD-UHFFFAOYSA-L zinc;2-hydroxybenzenesulfonate Chemical compound [Zn+2].OC1=CC=CC=C1S([O-])(=O)=O.OC1=CC=CC=C1S([O-])(=O)=O BOVNWDGXGNVNQD-UHFFFAOYSA-L 0.000 description 1
- ZNVKGUVDRSSWHV-UHFFFAOYSA-L zinc;4-hydroxybenzenesulfonate Chemical compound [Zn+2].OC1=CC=C(S([O-])(=O)=O)C=C1.OC1=CC=C(S([O-])(=O)=O)C=C1 ZNVKGUVDRSSWHV-UHFFFAOYSA-L 0.000 description 1
- 229910052726 zirconium Inorganic materials 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
- A61K8/84—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions otherwise than those involving only carbon-carbon unsaturated bonds
- A61K8/89—Polysiloxanes
- A61K8/891—Polysiloxanes saturated, e.g. dimethicone, phenyl trimethicone, C24-C28 methicone or stearyl dimethicone
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/02—Cosmetics or similar toiletry preparations characterised by special physical form
- A61K8/0216—Solid or semisolid forms
- A61K8/0229—Sticks
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/02—Cosmetics or similar toiletry preparations characterised by special physical form
- A61K8/04—Dispersions; Emulsions
- A61K8/046—Aerosols; Foams
-
- 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
- A61K8/19—Cosmetics or similar toiletry preparations characterised by the composition containing inorganic ingredients
- A61K8/20—Halogens; Compounds thereof
-
- 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
- A61K8/19—Cosmetics or similar toiletry preparations characterised by the composition containing inorganic ingredients
- A61K8/26—Aluminium; Compounds thereof
-
- 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
- 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
- A61K8/58—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing atoms other than carbon, hydrogen, halogen, oxygen, nitrogen, sulfur or phosphorus
- A61K8/585—Organosilicon compounds
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q15/00—Anti-perspirants or body deodorants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
- A61K2800/20—Chemical, physico-chemical or functional or structural properties of the composition as a whole
- A61K2800/24—Thermal properties
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
- A61K2800/20—Chemical, physico-chemical or functional or structural properties of the composition as a whole
- A61K2800/30—Characterized by the absence of a particular group of ingredients
- A61K2800/31—Anhydrous
Definitions
- the invention relates to cosmetic compositions for personal care, which contain a special oil mixture, and which are particularly suitable for the preparation as an antiperspirant.
- Washing, cleansing and caring for the human body is an important basic need, and cosmetic manufacturers are always trying to meet the ever-changing and evolving needs of consumers by providing novel and / or improved products.
- Cosmetic care products often comprise a higher proportion of one or more oils and, when in contact with textiles, can lead to the formation of stains on the textiles.
- other content and active ingredients contained in the care products such as, for example, dyes and / or perspiration-inhibiting (aluminum) salts
- the textile stains can be particularly stubborn and difficult to wash out.
- Make-up spots in the area of the collar or neckline and / or white residue in the underarm area of textiles are typical examples of hard-to-wash textile stains.
- White and / or yellow patches in the underarm area of textiles can be caused by the regular application of antiperspirants. These stains are probably caused by the formation of initially insoluble aluminum compounds on and within the textile fiber. The yellowing usually occurs with a time delay and is at least partially caused by oxidation of unsaturated fatty acids present as insoluble aluminum salts.
- other different factors can interact in unexpected ways and, for example, depending on the choice of perfume oil, the detergent and / or depending on the individual amount and composition of sweat promote the formation of pronounced yellow spots on textiles.
- insoluble compounds that can be absorbed by a textile. These insoluble compounds form white, hard residues, which usually show up after several soiling and washing cycles on the textile. These white residues are insoluble in water and can not be removed by a standard washing procedure. They are particularly noticeable on light or dark colored textiles. The clever choice of additives leads to a significantly lower or delay the formation of these insoluble deposits.
- oils with a high refractive index tend to accumulate in particular on cotton and form dark greasy or oily stains, which may adversely affect, among other things, the feel of the textiles in the soiled area.
- the use of predominantly volatile oils, such as cyclopentasiloxanes, in antiperspirants in turn, largely prevented the formation of wet, dark oil spots on the textiles, but did not prevent the formation of white residues caused by (aluminum) salt residues.
- volatile oils often do not have a satisfactory skin care effect and that, especially in high concentrations, they can result in aerosol applications to a dusty, low-focussing spray jet.
- Another aim was to formulate in particular oil-based, well-tolerated antiperspirants so that even after regular use they have less to no dark oil spots and / or white to yellow spots.
- the oil blends are readily incorporated into a variety of cosmetic care compositions and may even serve as the predominant basis for cosmetic compositions. They show an excellent skin care effect and a very good washability from textiles, especially cotton. In addition, when used in antiperspirants, the oil blends have an excellent effect of covering / reducing / preventing white aluminum salt residues.
- a first subject of the invention is therefore a cosmetic composition for personal care, which contains (in each case based on the total weight of the composition) an oil mixture in a total amount of 40 to 99 wt .-%, wherein the oil mixture
- ester which consists of at least one linear or branched, saturated or unsaturated mono-, di- or tricarboxylic acid having 3 to 30 carbon atoms, which may optionally contain one or more hydroxyl groups, and at least one linear or branched, saturated or unsaturated alcohol having 1 to 30 carbon atoms is formed,
- suitable cosmetic compositions for personal care are preferably skin treatment compositions which have a high content of hydrophobic active ingredients (oils), for example skin creams, make-ups, lipsticks, other decorative cosmetics such as eyeshadows, scrubs, skin lotions, deodorants, antiperspirants, hair oils, styling agents and / or pomades.
- hydrophobic active ingredients for example skin creams, make-ups, lipsticks, other decorative cosmetics such as eyeshadows, scrubs, skin lotions, deodorants, antiperspirants, hair oils, styling agents and / or pomades.
- cosmetic compositions which contain the abovementioned oil mixture in a proportion by weight of 40-99% by weight, more preferably 45-99% by weight, particularly preferably 50-99% by weight, very particularly preferably 55-99% by weight. Contain 99 wt .-% and in particular from 60 to 99 wt .-%.
- cosmetic compositions which comprise liquid oils a), b) and c) in the oil mixture.
- a liquid oil according to the invention is to be understood as meaning a liquid substance which is miscible under normal conditions with bidistilled water to less than 1% by weight.
- Normal conditions in the sense of the present application, a temperature of 20 ° C and a pressure of 1013.25 mbar.
- Polydimethylsiloxanes ensures a very good washability from textiles.
- high refractive index is understood to mean esters a) which have a refractive index (nD) of> 1, 420, preferably> 1, 425 and in particular> 1, 430 at 20 ° C.
- Oil mixtures which contain at least one ester from a first group a-1) and at least one ester from a second group of esters a-2) are particularly suitable.
- esters from group a-1) are preferably selected from esters of at least one branched alcohol having 4 to 20, more preferably 5 to 18 and in particular 6 to 16 carbon atoms and at least one linear or branched, saturated or unsaturated carboxylic acid with 8 to 24, preferably with 10 to 22 and particularly preferably with 12 to 20 carbon atoms.
- esters a-1 are 2-ethylhexyl laurate, 2-ethylhexyl myristate, 2-ethylhexyl palmitate, 2-ethylhexyl cocoate, 2-ethylhexyl stearate, 2-ethylhexyl isostearate, hexyldecyl laurate, hexyldecyl stearate, isopropyl myristate, isopropyl palmitate, isopropyl stearate, isooctyl stearate, isononyl isononanoate, isononyl stearate, Isotridecylnonanoat, 2-Octyldodecylpalmitat, Isocetylstearat and mixtures of these esters.
- Very particularly preferred esters a-1) are 2-ethylhexyl laurate, 2-ethylhexyl myristate, 2-ethylhexyl palmitate, 2-ethylhexyl stearate, 2-ethylhexyl isostearate, isopropyl myristate and / or isopropyl palmitate.
- esters a-1 preference is furthermore given to those which are liquid under normal conditions and preferably have a boiling point> 120 ° C., more preferably> 130 ° C. and particularly preferably> 140 ° C.
- 2-ethylhexyl palmitate and isopropyl myristate are especially preferred.
- esters a-2) are all optical forms of esters consisting of at least one C 2 -C 7 mono-, di- or tricarboxylic acid, which may optionally contain one or more hydroxyl groups, and at least one linear or branched, saturated or unsaturated alcohol having 1 to 10, preferably having 1 to 7 and in particular having 1 to 4 carbon atoms can be formed.
- esters a-2) selected from methyl, ethyl, n-propyl, isopropyl, n-butyl, 2-butyl or tert-butyl esters of glycolic acid, lactic acid, malic acid, tartaric acid, citric acid, oxalic acid, malonic acid , Succinic acid, glutaric acid and / or adipic acid.
- Very particularly preferred esters a-2) are methyl, ethyl and isopropyl esters of lactic acid, tartaric acid, oxalic acid, malonic acid, succinic acid, adipic acid and citric acid, for example ethyl lactate, dimethyltartar, diethyl tartrate, dimethoxy oxalate, diethyl oxalate, dimethyl malonate, diethyl malonate, dimethyl succinate, diethyl succinate, Dimethyl adipate, diethyl adipate, diisopropyl adipate, trimethyl citrate and triethyl citrate.
- ethyl lactate dimethyltartar, diethyl tartrate, dimethoxy oxalate, diethyl oxalate, dimethyl malonate, diethyl malonate, dimethyl succinate, diethyl succinate, Dimethyl adipate, diethyl adipate, di
- esters a-2 those esters which are liquid under standard conditions and which preferably have a boiling point> 150 ° C., more preferably> 175 ° C., particularly preferably> 200 ° C. and in particular> 225 ° C., are very particularly preferred ,
- ester a-1 selected from 2-ethylhexyl laurate, 2-ethylhexyl myristate, 2-ethylhexyl palmitate, 2-ethylhexyl cocoate, 2-ethylhexyl stearate, 2-ethylhexyl isostearate, hexyldecyl laurate, hexyldecyl stearate, isopropyl myristate, isopropyl palmitate, isopropyl stearate, isooctyl stearate, isononyl isononanoate, isononyl stearate, Isotridecylnonanoat, 2-Octyldodecylpalmitat, Isocetylstearat and / or mixtures of these esters and
- ester a-2 selected from methyl, ethyl, n-propyl, isopropyl, n-butyl, 2-butyl or the tert-butyl esters of glycolic acid, lactic acid, malic acid, tartaric acid, citric acid, oxalic acid , Malonic acid, succinic acid, glutaric acid and / or adipic acid.
- cosmetic compositions according to the invention are characterized in that the oil mixture contains at least two different esters from group a-1).
- oil blends containing as ester a-1) 2-ethylhexyl palmitate and isopropyl myristate are especially preferred within this embodiment because of their excellent ability to cover white powder residues (such as aluminum salts).
- compositions characterized in that the oil mixture contains as esters a-2) a methyl or ethyl ester of tartaric acid, citric acid and / or oxalic acid, preferably a methyl or ethyl ester of citric acid and in particular triethyl citrate.
- a further particularly preferred embodiment of the invention is characterized in that the cosmetic compositions are used as esters a)
- a proportion of cyclic polydimethylsiloxanes in the cosmetic compositions according to the invention is required in order to lower the tendency of the ester oils a) to form dark oil stains on textiles, in particular on cotton textiles, and to promote the good washability of the compositions.
- Particularly suitable cyclic polydimethylsiloxanes b) are readily volatile and have a vapor pressure of ⁇ 2.5 hPa, more preferably ⁇ 2.0 hPa, particularly preferably ⁇ 1.5 hPa and in particular ⁇ 1.0 hPa at 20 ° C.
- cyclic polydimethylsiloxanes c) are hexamethylcyclotrisiloxane, octamethylcyclotetrasiloxane, decamethylcyclopentasiloxane and / or dodecamethylcyclohexanosiloxane.
- cosmetic compositions according to the invention are characterized in that the oil mixture contains at least one cyclic polydimethylsiloxane b) selected from hexamethylcyclotrisiloxane, octamethylcyclotetrasiloxane, decamethylcyclopentasiloxane and / or dodecamethylcyclohexasiloxane, preferably from decamethylcyclopentasiloxane.
- compositions according to the invention contain, as a constituent of the oil mixture, at least one linear polydimethylsiloxane which has a kinematic viscosity of less than 20 cSt at 25 ° C.
- an addition of low-viscosity linear polydimethylsiloxanes to the oil mixtures gives the oil mixtures and the compositions according to the invention particularly advantageous performance properties. These include, in particular, the rheological properties of the oil mixtures or of the cosmetic compositions according to the invention, such as the spreading behavior.
- addition of linear polydimethylsiloxanes having a kinematic viscosity of less than 20 cSt at 25 ° C promotes to the oil blends both the good washability of oil stains which can be caused by high oil refractive index ester oils and washability white stains on textiles caused by the deposition of aluminum salts from antiperspirants.
- Particularly suitable linear polydimethylsiloxanes c) preferably have a viscosity (determined at 25 ° C. according to Brookfield) in the range from 2 to 10 mPas, particularly preferably from 4 to 8 mPas.
- the kinematic viscosity of particularly preferred linear polydimethylsiloxanes c) at 25 ° C. is preferably less than 20 cSt, more preferably less than 15 cSt and most preferably less than 10 cSt.
- linear polydimethylsiloxanes c) are commercially available, for example under the trade name Xiameter ® PMX 200 Sil Fluid 5 CS by the company Dow Corning.
- compositions characterized in that the oil mixture contains at least one linear polydimethylsiloxane c) which at 25 ° C has a kinematic viscosity of less than 15 cSt, preferably less than 10 cSt.
- the textile adhesion of the cosmetic compositions according to the invention is particularly low if the oil mixture contains the ester oils a) in slight excess to the sum of the silicone oils b) and c).
- silicone oils b) and c) in certain proportions contribute to a poorer adhesion of the ester oils to textiles and significantly increase the leachability of the cosmetic compositions.
- an oil mixture containing the oils a), b) and c) in certain proportions can be incorporated very well into a large number of cosmetic compositions.
- the corresponding cosmetic compositions absorb very well into the skin and care for them.
- dimethicone 5 cSt.
- oil mixtures containing components a), b) and c) significantly improve the leachability of cosmetic compositions based on the oil mixtures.
- the oil mixtures also have particularly good rheological properties and also give the cosmetic compositions into which they can be incorporated, particularly good rheological properties, in particular a very good spreading behavior.
- oil mixtures can be produced with certain refractive indices, which have a very low textile adhesion and a very good washability from textiles.
- sampling is understood to mean the ability of a liquid substance to spread upon contact with a surface, and the spreit value can be used as a measure of the spreading behavior of a liquid substance on a surface as described in DE102013217316) and is usually expressed in mm 2/10 min.
- Oil blends with a Spreit determination of 14.5 cm2 / 5 minutes to less than 16.0 cm2 / 5 minutes (25 ° C) and a refractive index in a range of 1, 420 and 1, 430 are particularly well suited for uses in cosmetic Compositions for personal care, in particular suitable for use in antiperspirant compositions, because they ensure the cover particularly well
- the oil mixture is particularly suitable for use in anhydrous compositions
- compositions characterized in that they are substantially anhydrous.
- essentially anhydrous is understood according to the invention as meaning that the cosmetic compositions contain 0 to at most 3% by weight, preferably 0 to at most 2% by weight, of free water, based on the total composition.
- Water of hydration or similar molecularly bound water which may be present in the constituents used, in particular in optionally contained antiperspirant active ingredients, does not constitute free water for the purposes of the present application.
- compositions according to the invention are particularly suitable as an antiperspirant composition.
- the compositions according to the invention are therefore made up as an antiperspirant composition, preferably as an anhydrous antiperspirant stick or as an anhydrous antiperspirant aerosol.
- Antiperspirants usually contain an antiperspirant component, therefore, in a further preferred embodiment, it is advantageous if the cosmetic compositions according to the invention also contain an antiperspirant active substance, preferably an antiperspirant aluminum salt.
- a second aspect of the invention is an antiperspirant cosmetic composition which comprises at least one ester a) which comprises at least one linear or branched, saturated or unsaturated mono-, di- or tricarboxylic acid having 3 to 30 carbon atoms and optionally containing one or more hydroxyl groups can be formed, and at least one linear or branched, saturated or unsaturated alcohol having 1 to 30 carbon atoms, in an amount by weight of 10 to 50 wt .-% of the total weight of the composition,
- antiperspirant compositions are particularly preferred which are particularly preferred which are particularly preferred which are particularly preferred which are particularly preferred.
- Dodecamethylcyclohexasiloxane preferably from decamethylcyclopentasiloxane, From 1 to 20% by weight, preferably from 5 to 15% by weight, of a polydimethylsiloxane known under the INCI name Dimethicone which has a kinematic viscosity of less than 20 cSt, preferably less than 10 cSt, at 25 ° C., and 10 to 40 wt .-%, preferably 15 to 25 wt .-% of at least one antiperspirant aluminum salt.
- Antiperspirant active substances which are preferred according to the invention are the water-soluble astringent inorganic and organic salts of aluminum, zirconium and zinc or any desired mixtures of these salts.
- Particularly preferred antiperspirant active ingredients are selected from the aluminum chlorohydrates, for example aluminum sesquichlorohydrate, aluminum chlorohydrex-propylene glycol (PG) or polyethylene glycol (PEG), aluminum sesquichlorohydrex PG or -PEG, aluminum PG-dichlorhydrex or aluminum PEG-dichlorhydrex, aluminum hydroxide selected from the Aluminiumzirconium- chlorohydrates, such Aluminiumzirconiumtrichlorhydrat, Aluminiumzirconiumtetrachlorhydrat, Aluminiumzirconiumpentachlorhydrat, Aluminiumzirconiumoctachlorhydrat, the aluminum-zirconium chlorohydrate glycine complexes, such as Aluminiumzirconiumtrichlorhydrexglycin, aluminum zirconiumtetrachlorhydrexglycin,
- Water solubility is understood according to the invention to mean a solubility of at least 5% by weight in water at 20 ° C., that is to say amounts of at least 5 g of the antiperspirant active are soluble in 95 g of water at 20 ° C.
- the antiperspirant Active substances can be used as aqueous solutions.
- antiperspirant compositions according to the invention are characterized in that they contain as antiperspirant active ingredient at least one antiperspirant antiperspirant active ingredient, preferably selected from astringent aluminum salts, in particular aluminum chlorohydrate, aluminum quin chlorohydrate and / or aluminum chloride, in a total amount of 10-40% by weight, preferably from 12.5 to 30% by weight and in particular 15 to 25% by weight, the amounts given being based on the total weight of the antiperspirant composition.
- astringent aluminum salts in particular aluminum chlorohydrate, aluminum quin chlorohydrate and / or aluminum chloride
- the antiperspirant compositions of the second subject of the invention may further comprise at least one deodorizing agent, which may be selected from odor absorbers, deodorizing agents Ion exchangers, germ-inhibiting active substances, prebiotic components and inhibitors of the enzymes responsible for the sweat decomposition or, more preferably, combinations of these active substances.
- at least one deodorizing agent which may be selected from odor absorbers, deodorizing agents Ion exchangers, germ-inhibiting active substances, prebiotic components and inhibitors of the enzymes responsible for the sweat decomposition or, more preferably, combinations of these active substances.
- Silicates can serve as preferred odor absorbers, which also at the same time favorably support the rheological properties of the antiperspirant compositions.
- Particularly preferred silicates include, in particular, phyllosilicates, and among these, in particular, montmorillonite, kaolinite, IIit, beidellite, nontronite, saponite, hectorite, bentonite, smectite and talcum.
- Further particularly preferred odor absorbers are, for example, zeolites, zinc ricinoleate, cyclodextrins, certain metal oxides, such as. As alumina, and chlorophyll.
- Odor absorbers may preferably be present in the antiperspirant compositions in an amount of from 0.1 to 10% by weight, more preferably from 0.5 to 7% by weight and most preferably from 1 to 5% by weight, based in each case on Total weight of the antiperspirant compositions are used.
- Preferred antiperspirant compositions are characterized in that they further contain at least one odor absorber, preferably a silicate.
- Germ-inhibiting or antimicrobial active ingredients are understood as meaning those active ingredients which reduce the number of skin germs participating in the formation of the odor or inhibit their growth.
- These organisms include, but are not limited to, various species of the group of staphylococci (eg, Staphylococcus hominis), the group of corynebacteria (eg, Corynebacterium xerosis, Corynebacterium CDCG2), anaerococci (eg, Anaerococcus octavius), and micrococci.
- the odorant mixtures Protectate HR and Protectate MOD 2 from Symrise can preferably be used as germ-inhibiting or antimicrobial agents.
- the fragrance mixture Protectate HR from Symrise contains 25-50% by weight of phenoxyethanol, 5-10% by weight of 2-methyl-5-phenylpentan-1-ol with the common name Rosaphen, 34-70% by weight of 2-benzylheptane -1-ol with the common name Jasmol, 1 - 5 wt .-% 4-methoxybenzyl alcohol (anis alcohol) and 0.01 - 1 wt .-% 5-methyl-2-isopropylphenol (thymol).
- the fragrance mixture Protectate MOD 2 from Symrise contains 25-45% by weight of phenoxyethanol, 5-10% by weight of 2-methyl-5-phenylpentan-1-ol and 45-70% by weight of 2-benzyl-heptane 1-ol.
- organohalogen compounds and halides, quaternary ammonium compounds, a range of plant extracts and zinc compounds are preferred antimicrobial or antimicrobial agents.
- These include triclosan, chlorhexidine and chlorhexidine gluconate, 3,4,4'-trichlorocarbanilide, bromochlorophene, dichlorophen, chlorothymol, chloroxylenol, hexachlorophene, dichloro-m-xylenol, dequalinium chloride, domiphen bromide, ammonium phenolsulfonate, Benzalkonium halides, benzalkonium cetyl phosphate, benzalkonium saccharinates, benzethonium chloride, cetylpyridinium chloride, laurylpyridinium chloride, laurylisoquinolinium bromide, methylbenzedonium chloride.
- phenol, phenoxyethanol, disodium dihydroxyethylsulfosuccinyl undecylenate, sodium bicarbonate, zinc lactate, sodium phenolsulfonate and zinc phenolsulfonate, ketoglutaric acid, terpene alcohols such.
- Sensiva SC 50 ® Ex Schulke & Mayr
- Carbonklander of mono-, di- and triglycerol z. B. glycerol, diglycerol
- plant extracts lantibiotics preferred deodorant actives Sensiva SC 50 ® (ex Schulke & Mayr), Carbonklareester of mono-, di- and triglycerol (z. B. glycerol, diglycerol), as well as plant extracts lantibiotics.
- deodorizing agents are selected from so-called prebiotically active components, which are understood to mean those components which inhibit only or at least predominantly the odor-producing germs of the skin microflora, but not the desired ones, that is to say the non-odor-forming germs which form a healthy skin microflora belong.
- active ingredients which are disclosed in the published patent applications DE 10333245 and DE 10 2004 01 1 968 as prebiotically effective, including conifer extracts, in particular from the group of Pinaceae, and plant extracts from the group of Sapindaceae, Araliaceae, Lamiaceae and Saxifragaceae, in particular extracts from Picea spp., Paullinia sp. , Panax sp. , Lamium album or Ribes nigrum and mixtures of these substances.
- deodorizing active ingredients are selected from the germ-inhibiting perfume oils and the Deosafe perfume oils, which are available from Symrise, formerly Haarmann and Reimer.
- Deodorizing enzyme inhibitors are those substances which inhibit the enzymes responsible for the sweat decomposition, in particular the arylsulfatase, ⁇ -glucuronidase, aminoacylase, ester-cleaving lipases and lipoxygenase, with zinc glycinate being preferred.
- the one or more of the above-mentioned deodorizing agent (s) may be used in the antiperspirant compositions of the second invention preferably in a total amount of 0.1-10 wt%, more preferably 0.2-7.5 wt% preferably from 0.3 to 5 wt .-% and particularly preferably from 0.5 to 3.0 wt .-%, based on the total weight of the composition, be contained.
- compositions according to the invention are characterized in that they contain at least one encapsulated and / or at least one non-encapsulated perfume.
- the encapsulation of the fragrances may preferably be selected such that it comprises at least one water-soluble encapsulation material.
- the water-soluble encapsulation material opens a certain time after application, and the encapsulated fragrance and optionally other encapsulated active substances, for example skin-cooling active ingredients, are released after the application with a time delay.
- Encapsulated and non-encapsulated fragrances may be identical or different.
- Particularly preferred antiperspirant compositions are characterized in that they contain at least one encapsulated and at least one non-encapsulated perfume, which are different from one another.
- Preferred antiperspirant compositions are characterized in that they contain at least one non-encapsulated perfume in a total amount of 0.1 to 3 wt.%, Preferably 0.2 to 1.5 wt.% And particularly preferably 0.4 to 1 wt. %, in each case based on the total weight of the aerosol composition.
- compositions are characterized in that they contain at least one encapsulated perfume in a total amount of 0.01-2% by weight, preferably 0.1-1.0% by weight and more preferably 0.25-0.5% by weight %, in each case based on the total weight of the aerosol composition.
- fragrances or perfume oils fragrance compounds are particularly preferred, for.
- ethers, aldehydes, ketones, alcohols and hydrocarbons are used.
- the preferred phenolic fragrance compounds include, for. B. carvacrol.
- Preferred fragrance compounds of the ester type are e.g.
- Benzyl acetate methyl anthranilate, ortho-t-butylcyclohexyl acetate, p-tert-butylcyclohexyl acetate, diethyl phthalate, nonanediol-1,3-diacetate, iso-nonylacetate, iso-nonylformate, phenylethylphenylacetate, phenoxyethylisobutyrate, linalylacetate, dimethylbenzylcarbinylacetate, phenylethylacetate, linalylbenzoate, benzylformate .
- the preferred ethers include, for example, benzyl ethyl ether, to the preferred aldehydes z.
- perfume oils may also contain natural fragrance mixtures such as are available from plant or animal sources, e.g. Pine, citrus, jasmine, ylang-ylang, rose, or lily oil.
- essential oils of lower volatility which are mostly used as aroma components, are particularly preferred as perfume oils, for.
- Preferred capsule material are water-soluble polymers such as starch, physically and / or chemically modified starches, cellulose derivatives, such as. As carboxymethylcellulose, methylcellulose, hydroxyethylcellulose or hydroxypropylmethylcellulose, carrageenans, alginates, maltodextrins, dextrins, vegetable gums, pectins, xanthans, polyvinyl acetate and polyvinyl alcohol, polyvinylpyrrolidine, polyamides, polyesters and homopolymers and copolymers of monomers selected from acrylic acid, methacrylic acid, maleic acid , Fumaric acid, itaconic acid and the esters and the salts of these acids, as well as any mixtures of these polymers.
- cellulose derivatives such as.
- Particularly preferred capsule materials are chemically modified starches, in particular aluminum starch octenylsuccinate, eg. The commercial product Dry Flo Plus from National Starch, or sodium starch octenylsuccinate, e.g. The commercial product Tylose H 10 from Clariant, furthermore the carboxymethylcellulose, carboxymethylcellulose, methylcellulose, hydroxyethylcellulose and hydroxypropylmethylcellulose, furthermore carrageenans, alginates and maltodextrins, as well as any mixtures of these polymers.
- aluminum starch octenylsuccinate eg. The commercial product Dry Flo Plus from National Starch
- sodium starch octenylsuccinate e.g. The commercial product Tylose H 10 from Clariant, furthermore the carboxymethylcellulose, carboxymethylcellulose, methylcellulose, hydroxyethylcellulose and hydroxypropylmethylcellulose, furthermore carrageenans, alginates and maltodextrins, as well as any mixture
- Particularly preferred capsule materials are polymer blends which consist of chemically modified starches and / or hydroxyethyl cellulose and a proportion of 0.2-2% by weight of alginates and / or carrageenans.
- the encapsulation can be carried out by known methods. Corresponding methods are for. Disclosed in K. Master, Spray Drying Handbook, 3rd Ed., John Wiley, 1979.
- a water-based mixture comprising about 20-50% by weight of the polymeric encapsulating material, about 0, is prepared. 1 to 2.0% by weight of an emulsifier, about 5 to 20% by weight of the perfume oil to be encapsulated and / or the skin-cooling active ingredient to be encapsulated and about 40 to 60% by weight of water.
- This mixture is homogenized and then spray-dried.
- the active ingredient-loaded capsules are thus obtained as a fine powder having a particle diameter of 1 to 150 ⁇ m, preferably 20 to 80 ⁇ m, particularly preferably 5 to 50 ⁇ m.
- the microencapsulation is carried out by coacervation, wherein the carrier is preferably formed from gelatin.
- the capsule material consisting of water-soluble polymers and a low content of emulsifiers, allows a reversible "re-encapsulation" of the encapsulated perfume oils and skin-cooling agents.
- the re-encapsulation occurs in situ during the drying of the Skin following a perspiration period.
- Fragrance or perfume-free antiperspirant compositions may also be preferred in the present invention.
- compositions of the second subject of the invention are characterized in that at least one suspension or thickening agent, preferably selected from hydrophobic clay minerals and fumed silicic acids, containing.
- Preferred hydrophobized clay minerals are montmorillonites, hectorites and bentonites, in particular disteardimonium hectorites and quaternium-18 hectorites.
- the commercial thickeners provide these hydrophobic clay minerals in the form of a gel in Cyclomethicone and, if desired, an additional Olkomponente such. As propylene carbonate, ready.
- Further preferred thickeners are fumed silicas, eg. For example, the commercial products of the Aerosil ® series from Degussa.
- the antiperspirant compositions of the second aspect of the invention may preferably be formulated as anhydrous stick preparations or as an anhydrous antiperspirant aerosol.
- Anhydrous antiperspirant aerosols may be beneficial for some applications.
- suitable antiperspirant aerosols are preferably packaged in commercial aerosol cans.
- the cans can be tinplate or aluminum.
- the cans may be internally coated in order to minimize the risk of corrosion.
- the aerosol cans are preferably equipped with a suitable spray head. Depending on the spray head, discharge rates, based on fully filled cans, of 0.1 g / s to 2.0 g / s are preferred.
- a third aspect of the invention is the cosmetic use of a cosmetic composition according to the invention as a personal care product, in particular as an antiperspirant composition, with a reduced tendency to stain textiles on textiles and / or with improved washability from textiles.
- the formulations 1 .1, 1.2 and 1.3 are each filled in a weight ratio of 1: 4 with the propellant propane / butane (15/85) in aerosol cans. s the following commercial products were used:
- INCI name Arachidyl Alcohol
- Sasol INCI name PPG-14 butyl ether
- Dow INCI name Myristyl Myristate
- Croda INCI name Hydrogenated Castor Oil
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Abstract
Description
Claims
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE102015205477.2A DE102015205477A1 (en) | 2015-03-26 | 2015-03-26 | "Cosmetic preparations with low textile adhesion" |
| PCT/EP2016/054493 WO2016150671A1 (en) | 2015-03-26 | 2016-03-03 | Cosmetic preparations with low textile adhesion |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| EP3274055A1 true EP3274055A1 (en) | 2018-01-31 |
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Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EP16707465.7A Withdrawn EP3274055A1 (en) | 2015-03-26 | 2016-03-03 | Cosmetic preparations with low textile adhesion |
Country Status (4)
| Country | Link |
|---|---|
| US (1) | US20180042835A1 (en) |
| EP (1) | EP3274055A1 (en) |
| DE (1) | DE102015205477A1 (en) |
| WO (1) | WO2016150671A1 (en) |
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| DE102017220988A1 (en) | 2017-11-23 | 2019-05-23 | Henkel Ag & Co. Kgaa | Cosmetic compositions with reduced oily or greasy feel on the skin |
| DE102017223728A1 (en) * | 2017-12-22 | 2019-06-27 | Beiersdorf Ag | Topical preparation for the improvement of skin moisture |
| FR3101245B1 (en) | 2019-09-30 | 2023-07-28 | Henkel Ag & Co Kgaa | Deodorant emulsion for aerosols for reducing the problem of stains, deodorant comprising this emulsion and use of this deodorant |
Family Cites Families (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4511554A (en) * | 1980-06-02 | 1985-04-16 | Bristol-Myers Company | Non-staining antiperspirant stick composition |
| US5444096A (en) * | 1989-06-02 | 1995-08-22 | Helene Curtis, Inc. | Stable anhydrous topically-active composition and suspending agent therefor |
| CA2014633C (en) * | 1989-06-02 | 2000-07-18 | Andrew D. Mccrea | Stable anhydrous compositions for topical delivery of active materials |
| BR9106483A (en) * | 1990-05-30 | 1993-05-25 | Procter & Gamble | LIQUID ANTIPERSPIRANT COMPOSITES |
| US5635165A (en) * | 1995-09-27 | 1997-06-03 | Helene Curtis, Inc. | Antiperspirant deodorant compositions |
| DE102004011968A1 (en) | 2004-03-10 | 2005-09-29 | Henkel Kgaa | Cosmetic or pharmaceutical composition e.g. useful for promoting the growth of desirable skin microorganisms comprises a plant extract with prebiotic activity on the skin |
| DE10333245C5 (en) | 2003-07-21 | 2015-02-19 | Henkel Ag & Co. Kgaa | Prebiotic plant extracts |
| DE102010063250A1 (en) * | 2010-12-16 | 2012-06-21 | Henkel Ag & Co. Kgaa | Hydrous antiperspirant compositions with improved residue masking |
| DE102011083293A1 (en) * | 2011-09-23 | 2013-03-28 | Henkel Ag & Co. Kgaa | Anhydrous formulations with cooling effect |
| US9084764B2 (en) * | 2012-08-16 | 2015-07-21 | Exert Co. | Epidermal cooling |
| FR3006178B1 (en) * | 2013-05-30 | 2015-06-26 | Oreal | COSMETIC USE AS A DEODORANT ACTIVE OF A SILICY MATERIAL OBTAINED BY HYDROLYSIS AND CONDENSATION OF A TETRAALCOXYSILANE AND A C7-C20-ALKYL TRIALCOXYSILANE |
| DE102013217316A1 (en) | 2013-08-30 | 2015-03-05 | Henkel Ag & Co. Kgaa | Skin Care Oil |
-
2015
- 2015-03-26 DE DE102015205477.2A patent/DE102015205477A1/en not_active Withdrawn
-
2016
- 2016-03-03 US US15/554,435 patent/US20180042835A1/en not_active Abandoned
- 2016-03-03 WO PCT/EP2016/054493 patent/WO2016150671A1/en not_active Ceased
- 2016-03-03 EP EP16707465.7A patent/EP3274055A1/en not_active Withdrawn
Also Published As
| Publication number | Publication date |
|---|---|
| DE102015205477A1 (en) | 2016-09-29 |
| WO2016150671A1 (en) | 2016-09-29 |
| US20180042835A1 (en) | 2018-02-15 |
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