EP3038714A1 - Hautpflegeöl - Google Patents
HautpflegeölInfo
- Publication number
- EP3038714A1 EP3038714A1 EP14758078.1A EP14758078A EP3038714A1 EP 3038714 A1 EP3038714 A1 EP 3038714A1 EP 14758078 A EP14758078 A EP 14758078A EP 3038714 A1 EP3038714 A1 EP 3038714A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- range
- oils
- liquid
- spreading value
- liquid oil
- 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.)
- Ceased
Links
- 239000003921 oil Substances 0.000 claims abstract description 238
- 239000007788 liquid Substances 0.000 claims abstract description 166
- 239000002537 cosmetic Substances 0.000 claims abstract description 88
- 239000000203 mixture Substances 0.000 claims description 98
- 238000003892 spreading Methods 0.000 claims description 94
- 125000000217 alkyl group Chemical group 0.000 claims description 92
- 150000001875 compounds Chemical class 0.000 claims description 70
- 125000004432 carbon atom Chemical group C* 0.000 claims description 57
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 claims description 24
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 24
- 229930195729 fatty acid Natural products 0.000 claims description 24
- 239000000194 fatty acid Substances 0.000 claims description 24
- 150000002148 esters Chemical class 0.000 claims description 21
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 20
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 15
- -1 C20 fatty acid Chemical class 0.000 claims description 10
- CMBYOWLFQAFZCP-UHFFFAOYSA-N Hexyl dodecanoate Chemical compound CCCCCCCCCCCC(=O)OCCCCCC CMBYOWLFQAFZCP-UHFFFAOYSA-N 0.000 claims description 6
- 229940100463 hexyl laurate Drugs 0.000 claims description 6
- 125000001183 hydrocarbyl group Chemical group 0.000 claims description 5
- 239000003795 chemical substances by application Substances 0.000 abstract description 5
- 238000001035 drying Methods 0.000 abstract description 4
- 230000035807 sensation Effects 0.000 abstract 1
- 235000019198 oils Nutrition 0.000 description 213
- 150000002430 hydrocarbons Chemical group 0.000 description 35
- 150000004665 fatty acids Chemical class 0.000 description 15
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 15
- ZSIAUFGUXNUGDI-UHFFFAOYSA-N hexan-1-ol Chemical compound CCCCCCO ZSIAUFGUXNUGDI-UHFFFAOYSA-N 0.000 description 8
- 239000004480 active ingredient Substances 0.000 description 7
- 239000000047 product Substances 0.000 description 7
- 239000000126 substance Substances 0.000 description 7
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 6
- JXPHIHWXMBYJAU-UHFFFAOYSA-N 7-methoxy-2,2-dimethyl-3,4-dihydrochromen-6-ol Chemical compound O1C(C)(C)CCC2=C1C=C(OC)C(O)=C2 JXPHIHWXMBYJAU-UHFFFAOYSA-N 0.000 description 5
- 239000000839 emulsion Substances 0.000 description 5
- 239000012528 membrane Substances 0.000 description 5
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 4
- AMQJEAYHLZJPGS-UHFFFAOYSA-N N-Pentanol Chemical compound CCCCCO AMQJEAYHLZJPGS-UHFFFAOYSA-N 0.000 description 4
- DKGAVHZHDRPRBM-UHFFFAOYSA-N Tert-Butanol Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 description 4
- BTANRVKWQNVYAZ-UHFFFAOYSA-N butan-2-ol Chemical compound CCC(C)O BTANRVKWQNVYAZ-UHFFFAOYSA-N 0.000 description 4
- 235000021466 carotenoid Nutrition 0.000 description 4
- 150000001747 carotenoids Chemical class 0.000 description 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 4
- OENHQHLEOONYIE-UKMVMLAPSA-N all-trans beta-carotene Natural products CC=1CCCC(C)(C)C=1/C=C/C(/C)=C/C=C/C(/C)=C/C=C/C=C(C)C=CC=C(C)C=CC1=C(C)CCCC1(C)C OENHQHLEOONYIE-UKMVMLAPSA-N 0.000 description 3
- 235000010323 ascorbic acid Nutrition 0.000 description 3
- 229960005070 ascorbic acid Drugs 0.000 description 3
- 239000011668 ascorbic acid Substances 0.000 description 3
- 235000013734 beta-carotene Nutrition 0.000 description 3
- 239000011648 beta-carotene Substances 0.000 description 3
- TUPZEYHYWIEDIH-WAIFQNFQSA-N beta-carotene Natural products CC(=C/C=C/C=C(C)/C=C/C=C(C)/C=C/C1=C(C)CCCC1(C)C)C=CC=C(/C)C=CC2=CCCCC2(C)C TUPZEYHYWIEDIH-WAIFQNFQSA-N 0.000 description 3
- 229960002747 betacarotene Drugs 0.000 description 3
- 150000001746 carotenes Chemical class 0.000 description 3
- 235000005473 carotenes Nutrition 0.000 description 3
- 239000013065 commercial product Substances 0.000 description 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 3
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 3
- 239000000758 substrate Substances 0.000 description 3
- PVJXQWMBHUOOCK-UHFFFAOYSA-N tetradecyl decanoate Chemical compound CCCCCCCCCCCCCCOC(=O)CCCCCCCCC PVJXQWMBHUOOCK-UHFFFAOYSA-N 0.000 description 3
- 238000012876 topography Methods 0.000 description 3
- OENHQHLEOONYIE-JLTXGRSLSA-N β-Carotene Chemical compound CC=1CCCC(C)(C)C=1\C=C\C(\C)=C\C=C\C(\C)=C\C=C\C=C(/C)\C=C\C=C(/C)\C=C\C1=C(C)CCCC1(C)C OENHQHLEOONYIE-JLTXGRSLSA-N 0.000 description 3
- 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 description 2
- SFAAOBGYWOUHLU-UHFFFAOYSA-N 2-ethylhexyl hexadecanoate Chemical compound CCCCCCCCCCCCCCCC(=O)OCC(CC)CCCC SFAAOBGYWOUHLU-UHFFFAOYSA-N 0.000 description 2
- QAQJMLQRFWZOBN-LAUBAEHRSA-N L-ascorbyl-6-palmitate Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@H](O)[C@H]1OC(=O)C(O)=C1O QAQJMLQRFWZOBN-LAUBAEHRSA-N 0.000 description 2
- 239000011786 L-ascorbyl-6-palmitate Substances 0.000 description 2
- UPYKUZBSLRQECL-UKMVMLAPSA-N Lycopene Natural products CC(=C/C=C/C=C(C)/C=C/C=C(C)/C=C/C1C(=C)CCCC1(C)C)C=CC=C(/C)C=CC2C(=C)CCCC2(C)C UPYKUZBSLRQECL-UKMVMLAPSA-N 0.000 description 2
- 235000010385 ascorbyl palmitate Nutrition 0.000 description 2
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid group Chemical group C(C1=CC=CC=C1)(=O)O WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 2
- 239000003581 cosmetic carrier Substances 0.000 description 2
- PKPOVTYZGGYDIJ-UHFFFAOYSA-N dioctyl carbonate Chemical compound CCCCCCCCOC(=O)OCCCCCCCC PKPOVTYZGGYDIJ-UHFFFAOYSA-N 0.000 description 2
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 2
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 2
- 229940089456 isopropyl stearate Drugs 0.000 description 2
- 150000002632 lipids Chemical class 0.000 description 2
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 2
- ZPWFUIUNWDIYCJ-UHFFFAOYSA-N propan-2-yl octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OC(C)C ZPWFUIUNWDIYCJ-UHFFFAOYSA-N 0.000 description 2
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 125000001424 substituent group Chemical group 0.000 description 2
- GYSCBCSGKXNZRH-UHFFFAOYSA-N 1-benzothiophene-2-carboxamide Chemical compound C1=CC=C2SC(C(=O)N)=CC2=C1 GYSCBCSGKXNZRH-UHFFFAOYSA-N 0.000 description 1
- OPJWPPVYCOPDCM-UHFFFAOYSA-N 2-ethylhexyl octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(CC)CCCC OPJWPPVYCOPDCM-UHFFFAOYSA-N 0.000 description 1
- GRXOKLJPWSYWIA-UHFFFAOYSA-N 2-ethylhexyl tetradecanoate Chemical compound CCCCCCCCCCCCCC(=O)OCC(CC)CCCC GRXOKLJPWSYWIA-UHFFFAOYSA-N 0.000 description 1
- JMOLZNNXZPAGBH-UHFFFAOYSA-M 2-hexyldecanoate Chemical compound CCCCCCCCC(C([O-])=O)CCCCCC JMOLZNNXZPAGBH-UHFFFAOYSA-M 0.000 description 1
- LEACJMVNYZDSKR-UHFFFAOYSA-N 2-octyldodecan-1-ol Chemical compound CCCCCCCCCCC(CO)CCCCCCCC LEACJMVNYZDSKR-UHFFFAOYSA-N 0.000 description 1
- HIQIXEFWDLTDED-UHFFFAOYSA-N 4-hydroxy-1-piperidin-4-ylpyrrolidin-2-one Chemical compound O=C1CC(O)CN1C1CCNCC1 HIQIXEFWDLTDED-UHFFFAOYSA-N 0.000 description 1
- 235000019489 Almond oil Nutrition 0.000 description 1
- 239000005711 Benzoic acid Substances 0.000 description 1
- 125000006539 C12 alkyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- GHVNFZFCNZKVNT-UHFFFAOYSA-N Decanoic acid Natural products CCCCCCCCCC(O)=O GHVNFZFCNZKVNT-UHFFFAOYSA-N 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- 238000007869 Guerbet synthesis reaction Methods 0.000 description 1
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical group CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 1
- JEVVKJMRZMXFBT-XWDZUXABSA-N Lycophyll Natural products OC/C(=C/CC/C(=C\C=C\C(=C/C=C/C(=C\C=C\C=C(/C=C/C=C(\C=C\C=C(/CC/C=C(/CO)\C)\C)/C)\C)/C)\C)/C)/C JEVVKJMRZMXFBT-XWDZUXABSA-N 0.000 description 1
- 235000018330 Macadamia integrifolia Nutrition 0.000 description 1
- 240000000912 Macadamia tetraphylla Species 0.000 description 1
- 235000003800 Macadamia tetraphylla Nutrition 0.000 description 1
- 240000003935 Sclerocarya birrea Species 0.000 description 1
- 235000001836 Sclerocarya caffra Nutrition 0.000 description 1
- OEWBEINAQKIQLZ-CMRBMDBWSA-N [(2s)-2-[(2r)-3,4-bis(2-hexyldecanoyloxy)-5-oxo-2h-furan-2-yl]-2-(2-hexyldecanoyloxy)ethyl] 2-hexyldecanoate Chemical compound CCCCCCCCC(CCCCCC)C(=O)OC[C@H](OC(=O)C(CCCCCC)CCCCCCCC)[C@H]1OC(=O)C(OC(=O)C(CCCCCC)CCCCCCCC)=C1OC(=O)C(CCCCCC)CCCCCCCC OEWBEINAQKIQLZ-CMRBMDBWSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 239000008168 almond oil Substances 0.000 description 1
- 239000010476 amaranth oil Substances 0.000 description 1
- BTFJIXJJCSYFAL-UHFFFAOYSA-N arachidyl alcohol Natural products CCCCCCCCCCCCCCCCCCCCO BTFJIXJJCSYFAL-UHFFFAOYSA-N 0.000 description 1
- 239000010478 argan oil Substances 0.000 description 1
- 239000000823 artificial membrane Substances 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 235000010233 benzoic acid Nutrition 0.000 description 1
- 150000001559 benzoic acids Chemical class 0.000 description 1
- PXTQQOLKZBLYDY-UHFFFAOYSA-N bis(2-ethylhexyl) carbonate Chemical class CCCCC(CC)COC(=O)OCC(CC)CCCC PXTQQOLKZBLYDY-UHFFFAOYSA-N 0.000 description 1
- 150000008371 chromenes Chemical class 0.000 description 1
- 230000003750 conditioning effect Effects 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- 125000002704 decyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 229940117973 dimethylmethoxy chromanol Drugs 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 230000002500 effect on skin Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 230000001815 facial effect Effects 0.000 description 1
- 239000003925 fat Substances 0.000 description 1
- 210000000245 forearm Anatomy 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 230000036571 hydration Effects 0.000 description 1
- 238000006703 hydration reaction Methods 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- XUGNVMKQXJXZCD-UHFFFAOYSA-N isopropyl palmitate Chemical compound CCCCCCCCCCCCCCCC(=O)OC(C)C XUGNVMKQXJXZCD-UHFFFAOYSA-N 0.000 description 1
- 230000002045 lasting effect Effects 0.000 description 1
- 230000000670 limiting effect Effects 0.000 description 1
- 235000012680 lutein Nutrition 0.000 description 1
- 239000001656 lutein Substances 0.000 description 1
- 229960005375 lutein Drugs 0.000 description 1
- KBPHJBAIARWVSC-RGZFRNHPSA-N lutein Chemical compound C([C@H](O)CC=1C)C(C)(C)C=1\C=C\C(\C)=C\C=C\C(\C)=C\C=C\C=C(/C)\C=C\C=C(/C)\C=C\[C@H]1C(C)=C[C@H](O)CC1(C)C KBPHJBAIARWVSC-RGZFRNHPSA-N 0.000 description 1
- ORAKUVXRZWMARG-WZLJTJAWSA-N lutein Natural products CC(=C/C=C/C=C(C)/C=C/C=C(C)/C=C/C1=C(C)CCCC1(C)C)C=CC=C(/C)C=CC2C(=CC(O)CC2(C)C)C ORAKUVXRZWMARG-WZLJTJAWSA-N 0.000 description 1
- 235000012661 lycopene Nutrition 0.000 description 1
- 239000001751 lycopene Substances 0.000 description 1
- OAIJSZIZWZSQBC-GYZMGTAESA-N lycopene Chemical compound CC(C)=CCC\C(C)=C\C=C\C(\C)=C\C=C\C(\C)=C\C=C\C=C(/C)\C=C\C=C(/C)\C=C\C=C(/C)CCC=C(C)C OAIJSZIZWZSQBC-GYZMGTAESA-N 0.000 description 1
- 229960004999 lycopene Drugs 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 230000004060 metabolic process Effects 0.000 description 1
- 239000010466 nut oil Substances 0.000 description 1
- BARWIPMJPCRCTP-CLFAGFIQSA-N oleyl oleate Chemical compound CCCCCCCC\C=C/CCCCCCCCOC(=O)CCCCCCC\C=C/CCCCCCCC BARWIPMJPCRCTP-CLFAGFIQSA-N 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 239000002304 perfume Substances 0.000 description 1
- 230000003389 potentiating effect Effects 0.000 description 1
- 102000004169 proteins and genes Human genes 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 230000009759 skin aging Effects 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 230000009897 systematic effect Effects 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- ZCIHMQAPACOQHT-ZGMPDRQDSA-N trans-isorenieratene Natural products CC(=C/C=C/C=C(C)/C=C/C=C(C)/C=C/c1c(C)ccc(C)c1C)C=CC=C(/C)C=Cc2c(C)ccc(C)c2C ZCIHMQAPACOQHT-ZGMPDRQDSA-N 0.000 description 1
- KBPHJBAIARWVSC-XQIHNALSSA-N trans-lutein Natural products CC(=C/C=C/C=C(C)/C=C/C=C(C)/C=C/C1=C(C)CC(O)CC1(C)C)C=CC=C(/C)C=CC2C(=CC(O)CC2(C)C)C KBPHJBAIARWVSC-XQIHNALSSA-N 0.000 description 1
- NCYCYZXNIZJOKI-UHFFFAOYSA-N vitamin A aldehyde Natural products O=CC=C(C)C=CC=C(C)C=CC1=C(C)CCCC1(C)C NCYCYZXNIZJOKI-UHFFFAOYSA-N 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
- FJHBOVDFOQMZRV-XQIHNALSSA-N xanthophyll Natural products CC(=C/C=C/C=C(C)/C=C/C=C(C)/C=C/C1=C(C)CC(O)CC1(C)C)C=CC=C(/C)C=CC2C=C(C)C(O)CC2(C)C FJHBOVDFOQMZRV-XQIHNALSSA-N 0.000 description 1
- 150000003735 xanthophylls Chemical class 0.000 description 1
- 235000008210 xanthophylls Nutrition 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/33—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
- A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
- A61K8/34—Alcohols
- A61K8/342—Alcohols having more than seven atoms in an unbroken chain
-
- 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
- A61K8/375—Esters of carboxylic acids the alcohol moiety containing more than one hydroxy group
-
- 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
- A61K8/92—Oils, fats or waxes; Derivatives thereof, e.g. hydrogenation products thereof
- A61K8/922—Oils, fats or waxes; Derivatives thereof, e.g. hydrogenation products thereof of vegetable origin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q19/00—Preparations for care of the skin
-
- 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
- A61K2800/40—Chemical, physico-chemical or functional or structural properties of particular ingredients
- A61K2800/59—Mixtures
- A61K2800/592—Mixtures of compounds complementing their respective functions
- A61K2800/5922—At least two compounds being classified in the same subclass of A61K8/18
Definitions
- the present invention relates to dermal cosmetics, in particular to compositions based predominantly on liquid oil.
- these skincare compositions comprise active ingredients which, for example, influence the metabolism of the skin and thus change their aesthetic appearance, for example, provide the skin with fats or oils or, for example, protect it from sunlight or free radicals.
- Emulsions have proven to be effective as potent cosmetic carriers because they can mediate both lipophilic and hydrophilic active ingredients.
- Corresponding emulsions are usually oil-in-water emulsions or water-in-oil emulsions.
- skin care products which comprise a cosmetic base based on oils but are not present as an emulsion may be suitable in particular.
- Such care oils should make the skin smooth and supple, nourish it intensively and protect it from drying out.
- the elasticity of the skin and the firmness of the skin should also be optimized.
- oil-based cosmetics spread well over the substrate, such as the skin, the skin slowly absorbs the oil. This results in a lasting presence of an oil film on the skin.
- the oil film adversely affects the feel of the skin.
- the skin feels oily to sticky.
- the skin treated with the care oil comes into contact with clothing and the clothing absorbs the oil film in whole or in part. In this way, on the one hand clothes are soiled and on the other hand reduces the effectiveness of the cosmetic on the skin.
- the cosmetic should be quickly absorbed by the skin and provide optimal care, especially on at least one of the aforementioned care parameters.
- a first subject of the invention are therefore cosmetic compositions containing - in each case based on the total weight of the composition - liquid oils in a total amount of 80 to 99.5 wt .-%, being as liquid oils
- normal conditions are a temperature of 20 ° C. and a pressure of 1013.25 mbar. Melting point data likewise relate to a pressure of 1013.25 mbar.
- composition of the invention necessarily contains one or more liquid oils in said total amount.
- a liquid oil according to the invention is to be understood as meaning a liquid substance which is miscible under normal conditions in bidistilled water to less than 1% by weight.
- free water used in the context of embodiments of the invention is understood in the sense that the content of water of crystallization, water of hydration or similar molecularly bound water which may be contained in the constituents used, in particular in the particulate-dispersed solids, in the sense the present application is not free water.
- the liquid oils containing in the cosmetic composition according to the invention have special Spreitagonist.
- Spreading is the ability of a liquid substance to spread upon contact with a surface on that surface.
- the spread value serves as a measure of the spreading behavior of a liquid substance on a surface.
- the spread value is determined as the area measured in mm 2 , which has a nearly point-like applied to a horizontal surface liquid after 10 minutes dwell time on this surface.
- skin or a substance mimicking the surface topography of the skin was used as the surface.
- the Spreitwert at 25 ° C ambient temperature and 60% relative humidity
- Vitro-Skin ® the company IMS Inc (Portland, USA)
- the Vitro-Skin ® membrane contains protein and lipid components and displays topography, pH, critical surface tension and ionic strength, all modeled on human skin.
- Vitro-Skin ® has a constant N-19 topography.
- the constant wetting properties of each Vitro-Skin ® membrane are modeled on the skin of the human back. After a residence time of 10 minutes, the spreading area on the membrane was measured. There were six measurements per liquid oil.
- the arithmetic mean of these six determinations constitutes the spreading value according to the invention (25 ° C.).
- the spread value on the human skin (forearm) was measured mutatis mutandis, but with the following deviations:
- the relative spread value was determined against decanoic acid tetetradecyl ester as an external standard.
- a true impression was taken after 10 minutes of the spread lipid with a transparent paper and the area determined.
- the spread value determined for each of the six test persons was calculated according to the following formula:
- the arithmetic mean of the six determinations forms the spreading value according to the invention (25 ° C.).
- the average spread value of the external standard decanoic acid tetradecyl ester used in the calculation was previously determined on 20 test persons and the arithmetic mean of the measured area was calculated.
- the cosmetic composition as a liquid oil with a water coverage (25 ° C) in a range of 100 mm 2/10 min to less than 800 mm 2/10 min, at least one liquid compound of the general formula (I contains)
- R is a C2 to O0 hydrocarbon group (preferably alkyl), in particular octyl, and R 2 is a C4 to C12 hydrocarbon group (preferably alkyl).
- R is preferably a C2 to O0-alkyl group, in particular octyl, and R 2 is a C4 to C12-alkyl group.
- the cosmetic composition as a liquid oil having a spreading value (25 ° C) in a range of 100 mm 2/10 min to less than 800 mm 2/10 min, at least one liquid compound of the general formula (II contains)
- R 3 is a C 10 to C 16 hydrocarbon group, in particular C 12 to C 15 hydrocarbon group.
- R 3 is preferably a C 10 to C 16 -alkyl group, in particular C 12 to C 15 -alkyl group.
- Preferred liquid oils of the formula (II) are selected from the benzoic acid esters of linear or branched C 16 -alkanols. Particularly preferred are benzoic C12-C15-alkyl esters, z. B. available as a commercial product Finsolv ® TN, benzoic acid isostearyl, z. B. available as a commercial product Finsolv ® SB.
- the cosmetic composition in a particularly preferred embodiment includes the cosmetic composition as a liquid oil having a spreading value (25 ° C) in a range of 100 mm 2/10 min to less than 800 mm 2/10 min, at least one liquid compound of the general formula ( I) (vide supra) together with at least one compound of general formula (II) (vide supra).
- the preferred embodiments of the compounds of the formulas (I) and (II) are also preferred.
- At least one natural oil such as almond oil, amaranth oil, marula, macadamia nut oil, argan oil
- a liquid oil having a spreading value (25 ° C) in a range of 100 mm 2/10 min to less than 800 mm 2/10 minutes is according to the invention.
- Liquid oils having a spreading value (25 ° C) of less than 100 mm 2/10 minutes should not be possible or used in the inventive cosmetic products in very small quantities. It is therefore preferred to use such liquid oils in amounts of 0 to 0.25% by weight, in particular 0 to 0.05% by weight.
- the cosmetic composition as a liquid oil having a spreading value (25 ° C) in a range of 800 mm 2/10 min, containing up below 1050 mm 2/10 minutes at least one compound of formula (III)
- R 4 is an alkyl group having 2 to 4 carbon atoms, in particular ethyl
- R 5 is an alkyl group having 4 to 6 carbon atoms
- R 6 is an alkyl group having 7 to 17 carbon atoms.
- liquid oils according to formula (III) from at least one compound in which R 4 is an ethyl group, R 5 is an n-butyl group and R 6 is an alkyl group having 7 to 15 carbon atoms (especially one Alkyl group with 1 1 to 15 carbon atoms.
- Preferred compounds of formula (III) are selected from 2-ethylhexyl palmitate, 2-ethylhexyl stearate, 2-ethylhexyl myristate or mixtures thereof. Very particular preference is given to 2-ethylhexyl palmitate.
- the cosmetic composition as a liquid oil having a spreading value (25 ° C) in a range of 800 mm 2/10 min to below 1050 mm 2/10 min, at least one ester of isopropanol with a Ci6 to 020 fatty acid contains.
- Preferred compounds of the esters of isopropanol with a C 16 to C 20 fatty acid are selected from isopropyl stearate, isopropyl palmitate, isopropyl myristate and mixtures thereof. Very particular preference is isopropyl stearate.
- the cosmetic composition in a particularly preferred embodiment includes the cosmetic composition as a liquid oil having a spreading value (25 ° C) in a range of 800 mm 2/10 min to below 1050 mm 2/10 min, at least one liquid compound of the general formula ( III) (vide supra) together with at least one ester of isopropanol with a Ci6 to C2o fatty acid (vide supra).
- the preferred embodiments of the compounds of formula (III) and the ester of isopropanol with a C 16 to C 20 fatty acid (vide supra) are also preferred.
- the cosmetic composition as a liquid oil having a spreading value (25 ° C) in a range of 1050 mm 2/10 minutes to 1800 mm 2/10 minutes at least one compound of formula (IV)
- R 7 and R 8 independently represent a linear or branched alkyl group having 6 to 10 carbon atoms, in particular a linear or branched alkyl group having 8 carbon atoms.
- Preferred compounds according to formula (IV) are selected from dicaprylyl carbonate (dioctyl carbonate), di (2-ethylhexyl) carbonates or mixtures thereof.
- dicaprylyl available for example with the trade name Cetiol CC ® from BASF SE.
- the cosmetic composition as a liquid oil having a spreading value (25 ° C) in a range of 1050 mm 2/10 minutes to 1800 mm 2/10 min
- at least one ester of a (C4 to C6) -Alkanol with a C16 to C2o fatty acid contains.
- Preferred (C4 to C6) alkanols are n-butanol, n-hexanol, tert-butanol, sec-butanol or n-pentanol. Particularly preferred is n-hexanol.
- a particularly preferred ester is hexyl laurate.
- the inventive cosmetic composition as a liquid oil having a spreading value (25 ° C) in a range of 1050 mm 2/10 minutes to 1800 mm 2/10 min, at least one liquid compound of the general formula ( IV) (vide supra) together with at least one ester of a (C4 to C6) -alkanol with a C16 to C20 fatty acid.
- Preferred (C4 to C6) alkanols are n-butanol, n-hexanol, tert-butanol, sec-butanol or n-pentanol. Particularly preferred is n-hexanol.
- a particularly preferred ester is hexyl laurate.
- the cosmetic agent according to the invention contains, based on the total weight of the composition, liquid oil in a total amount of from 85 to 99% by weight, in particular from 90 to 98% by weight.
- liquid oil with a water coverage (25 ° C) in a range of 800 mm 2/10 min to below 1050 mm 2/10 min, in a total amount of 35 to 50 Wt .-% included is preferably together with the preferred total amount of liquid oil having a spreading value (25 ° C) in a range of 100 mm 2/10 min to less than 800 mm 2/10 min (vide supra) combined.
- liquid oil with a water coverage by weight (25 ° C) in a range of 1050 mm 2/10 minutes to 1800 mm 2/10 minutes in a total amount of 12 to 22 .-% contain.
- This preferred total amount is preferably together with the preferred total amount of liquid oil having a spreading value (25 ° C) in a range of 100 mm 2/10 min to less than 800 mm 2/10 min (vide supra) combined.
- compositions according to the invention are each based on the total weight of the cosmetic agent
- liquid oil having a spreading value (25 ° C) in a range of 100 mm 2/10 min to less than 800 mm 2/10 min, in a total amount from 32 to 42 wt .-%,
- liquid oil having a spreading value (25 ° C) in a range of 800 mm 2/10 min to below 1050 mm 2/10 min, in a total amount of 35 to 50 wt .-%.
- liquid oil having a spreading value (25 ° C) in a range of 1050 mm 2/10 minutes to 1800 mm 2/10 min, in a total amount of 12 to 22 wt .-%, of.
- the total amount of the oils mentioned under (b) to the sum of the respective total amounts of the oils mentioned under (a) and (c) in the range of 1.5 to 1 to 1 to 2, particularly preferred between 1 .2 to 1 and 1 to 1.8, most preferably between 1 to 1.2 to 1 to 1.7.
- This preferred embodiment can in turn preferably be combined with one or more of the aforementioned preferred total amounts of the said liquid oils.
- the cosmetic compositions of the invention are preferably low in water to anhydrous, in particular they are anhydrous. It has proven advantageous if the cosmetic compositions according to the invention comprise free water in an amount of from 0 to 0.1% by weight, particularly preferably from 0 to 0.05, very particularly preferably from 0 to 0.01% by weight, most preferably from 0 to 0.001% by weight, based in each case on the total weight of the cosmetic composition.
- Cosmetic agents preferred according to the invention are transparent.
- a cosmetic product is considered to be transparent if, through a sample of the cosmetic product with a layer thickness d of 3 cm, a letter "A" (10 point size in Times New Roman font) 10 cm away from the sample is visible to the naked eye with the naked eye. is recognized.
- Particularly preferred embodiments Examples of the invention are characterized by the embodiments (A) to (P):
- R is a C2 to O0 hydrocarbon group (preferably alkyl), in particular octyl, and R 2 is a C4 to C12 hydrocarbon group (preferably alkyl),
- R preferably alkyl
- a C4 preferably alkyl stands for a C2 to Oo-hydrocarbon group
- R 3 is a C 10 to C 16 hydrocarbon group, in particular C 12 to C 15 hydrocarbon group,
- R is a C2 to O0 hydrocarbon group (preferably alkyl), in particular octyl, and R 2 is a C4 to C12 hydrocarbon group (preferably alkyl), and
- R 3 is a C10 to Ci6 hydrocarbyl group, especially C12 to C15 hydrocarbon group, is,
- R 4 is an alkyl group having 2 to 4 carbon atoms, in particular ethyl
- R 5 is an alkyl group having 4 to 6 carbon atoms
- R 6 is an alkyl group having 7 to 17 carbon atoms
- R is a C2 to O0 hydrocarbon group (preferably alkyl), in particular octyl, and R 2 is a C4 to C12 hydrocarbon group (preferably alkyl), and
- R 3 is a C 10 to C 16 hydrocarbon group, in particular C 12 to C 15 hydrocarbon group,
- R 4 is an alkyl group having 2 to 4 carbon atoms, in particular ethyl
- R 5 is an alkyl group having 4 to 6 carbon atoms
- R 6 is an alkyl group having 7 to 17 carbon atoms
- At least one further of these oils is selected from at least one ester of isopropanol with a C 16 to C 20 fatty acid,
- R is a C2 to O0 hydrocarbon group (preferably alkyl), in particular octyl, and R 2 is a C4 to C12 hydrocarbon group (preferably alkyl), and
- R 3 is a C 10 to C 16 hydrocarbon group, in particular C 12 to C 15 hydrocarbon group, , (b) at least two liquid oils having a spreading value (25 ° C) in a range of 800 mm 2/10 min to below 1050 mm 2/10 minutes wherein at least one of these oils selected from at least one compound of formula (III)
- R 4 is an alkyl group having 2 to 4 carbon atoms, in particular ethyl
- R 5 is an alkyl group having 4 to 6 carbon atoms
- R 6 is an alkyl group having 7 to 17 carbon atoms
- At least one further of these oils is selected from at least one ester of isopropanol with a C 16 to C 20 fatty acid,
- R 7 and R 8 independently of one another represent a linear or branched alkyl group having 6 to 10 carbon atoms, in particular a linear or branched alkyl group having 8 carbon atoms,
- R is a C2 to O0 hydrocarbon group (preferably alkyl), in particular octyl, and R 2 is a C4 to C12 hydrocarbon group (preferably alkyl), and
- R 3 is a C 10 to C 16 hydrocarbon group, in particular C 12 to C 15 hydrocarbon group,
- R is a C2 to Oo hydrocarbon group (preferably alkyl), in particular octyl, and R 2 is a C4 to C12 hydrocarbon group (preferably alkyl), (b) at least one liquid oil having a Spreitwert (25 ° C) in one range of 800 mm 2/10 min to below 1050 mm 2/10 minutes, (c) at least one liquid oil having a spreading value (25 ° C) in a range of 1050 mm 2/10 minutes to 1800 mm 2/10 minutes selected from at least one compound of formula (IV)
- R 7 and R 8 independently of one another represent a linear or branched alkyl group having 6 to 10 carbon atoms, in particular a linear or branched alkyl group having 8 carbon atoms,
- R preferably alkyl
- a C4 preferably alkyl stands for a C2 to oo-hydrocarbon group
- R 3 is a C 10 to C 16 hydrocarbon group, in particular C 12 to C 15 hydrocarbon group,
- R 4 is an alkyl group having 2 to 4 carbon atoms, in particular ethyl
- R 5 is an alkyl group having 4 to 6 carbon atoms
- R 6 is an alkyl group having 7 to 17 carbon atoms
- At least one further of these oils is selected from at least one ester of isopropanol with a C 16 to C 20 fatty acid,
- At least one further of these oils is selected from at least one ester of a (04 to C6) alkanol with a Ci6 to 020 fatty acid, in particular hexyl laurate, with the proviso that the weight ratio of the total amount mentioned under (a) Oils to the sum of the respective total amounts of the oils mentioned under (b) and (c) in the range from 1 to 3 to 1 to 1, preferably from 1 to 2.5 to 1 to 1.2, particularly preferably from 1 to 2 to 1 to 1.3, most preferably from 1 to 1.9 to 1 to 1 .4.
- composition containing in each case based on the total weight of the composition, liquid oils in a total amount of 80 to 99.5 wt .-%, (in particular from 85 to 99 wt .-%, in particular from 90 to 98 wt. %), characterized in that as liquid oils at least
- R is a C 2 to C 10 hydrocarbon group (preferably alkyl), in particular octyl, and R 2 is a C 4 to C 12 hydrocarbon group (preferably alkyl),
- R is a C2 to O0 hydrocarbon group (preferably alkyl), in particular octyl, and R 2 is a C4 to C12 hydrocarbon group (preferably alkyl), and
- R 3 is a C 10 to C 16 hydrocarbon group, in particular C 12 to C 15 hydrocarbon group,
- (c) min at least one liquid oil having a spreading value (25 ° C) in a range of 1050 mm 2/10 minutes to 1800 mm 2/10 with the proviso that the weight ratio of the total amount of the oils mentioned under (a) to the sum of the respective total amounts of the oils mentioned under (b) and (c) in the range of 1 to 3 to 1 to 1, preferably from 1 from 2.5 to 1 to 1.2, more preferably from 1 to 2 to 1 to 1 .3, most preferably from 1 to 1.9 to 1 to 1.4.
- R is a C2 to O0 hydrocarbon group (preferably alkyl), in particular octyl, and R 2 is a C4 to C12 hydrocarbon group (preferably alkyl), and
- R 3 is a C 10 to C 16 hydrocarbon group, in particular C 12 to C 15 hydrocarbon group,
- R 4 is an alkyl group having 2 to 4 carbon atoms, in particular ethyl
- R 5 is an alkyl group having 4 to 6 carbon atoms
- R 6 is an alkyl group having 7 to 17 carbon atoms
- (c) min at least one liquid oil having a spreading value (25 ° C) in a range of 1050 mm 2/10 minutes to 1800 mm 2/10 with the proviso that the weight ratio of the total amount of the oils mentioned under (a) to the sum of the respective total amounts of the oils mentioned under (b) and (c) in the range of 1 to 3 to 1 to 1, preferably from 1 from 2.5 to 1 to 1.2, more preferably from 1 to 2 to 1 to 1 .3, most preferably from 1 to 1.9 to 1 to 1.4.
- R is a C2 to O0 hydrocarbon group (preferably alkyl), in particular octyl, and R 2 is a C4 to C12 hydrocarbon group (preferably alkyl), and
- R 3 is a C10 to Ci6 hydrocarbyl group, especially C12 to C15 hydrocarbon group, is,
- liquid oil having a spreading value (25 ° C) in a range of 800 mm 2/10 min to below 1050 mm 2/10 minutes, wherein it is a mixture of a or more compounds of the formula (III)
- R 4 is an alkyl group having 2 to 4 carbon atoms, in particular ethyl
- R 5 is an alkyl group having 4 to 6 carbon atoms
- R 6 is an alkyl group having 7 to 17 carbon atoms
- R preferably alkyl
- a C4 preferably alkyl stands for a C2 to Oo-hydrocarbon group
- R 3 is a C 10 to C 16 hydrocarbon group, in particular C 12 to C 15 hydrocarbon group,
- liquid oil having a spreading value (25 ° C) in a range of 800 mm 2/10 min to below 1050 mm 2/10 minutes, wherein it is a mixture of a or more compounds of the formula (III)
- R 4 is an alkyl group having 2 to 4 carbon atoms, in particular ethyl
- R 5 is an alkyl group having 4 to 6 carbon atoms
- R 6 is an alkyl group having 7 to 17 carbon atoms, and selected from at least one ester of isopropanol with a C16 to C20 fatty acid,
- R 7 and R 8 independently of one another represent a linear or branched alkyl group having 6 to 10 carbon atoms, in particular a linear or branched alkyl group having 8 carbon atoms,
- R preferably alkyl
- a C4 preferably alkyl stands for a C2 to oo-hydrocarbon group
- R 3 is a C 10 to C 16 hydrocarbon group, in particular C 12 to C 15 hydrocarbon group,
- R 4 is an alkyl group having 2 to 4 carbon atoms, in particular ethyl
- R 5 is an alkyl group having 4 to 6 carbon atoms
- R 6 is an alkyl group having 7 to 17 carbon atoms
- R 7 and R 8 independently of one another represent a linear or branched alkyl group having 6 to 10 carbon atoms, in particular a linear or branched alkyl group having 8 carbon atoms,
- R preferably alkyl
- a C4 preferably alkyl stands for a C2 to oo-hydrocarbon group
- R 3 is a C 10 to C 16 hydrocarbon group, in particular C 12 to C 15 hydrocarbon group,
- R 7 and R 8 independently of one another represent a linear or branched alkyl group having 6 to 10 carbon atoms, in particular a linear or branched alkyl group having 8 carbon atoms,
- R is a C2 to O0 hydrocarbon group (preferably alkyl), especially octyl
- R 2 is a C4 to C12 hydrocarbon group (preferably alkyl)
- R 7 and R 8 independently of one another represent a linear or branched alkyl group having 6 to 10 carbon atoms, in particular a linear or branched alkyl group having 8 carbon atoms,
- Cosmetic agents preferred according to the invention additionally comprise at least one fatty acid ester of at least one linear or branched C 6 to C 18 fatty acid with ascorbic acid. It is again particularly preferred if the fatty acid ester of at least one linear or branched C 6 to C 18 fatty acid with ascorbic acid is selected from one or more compounds of ascorbyl tetraisopalmitate (also: ascorbyl tetrakis (2-hexyldecanoate)), ascorbyl palmitate (INCI name: ascorbyl palmitate ).
- Cosmetic agents preferred according to the invention additionally contain at least one carotenoid.
- Carotenoids which are suitable according to the invention include the carotenes (pure hydrocarbons) and the xanthophylls (oxygen-containing carotenes) whose backbone consists of eight isoprene units.
- Carotenoids which are particularly suitable according to the invention are selected from lutein, o carotene, ⁇ -carotene and lycopene. Very particular preference is given to ⁇ -carotene.
- Agents preferred according to the invention additionally contain at least one 6,7-disubstituted 2,2-dialkylchroman or chroma of the general formula (Cl) or (CM)
- R and R 2 independently of one another are an OH group, a methoxy group or a CFsCh O group and R 3 and R 4 independently of one another a (C 1 to C 4 ) -alkyl group represent.
- R and R 2 according to formulas (Cl) and (CM) are independently selected from an OH group, a methoxy group and a CFsChbO group.
- R and R 2 according to formulas (Cl) and (CM) are independently selected from an OH group and a methoxy group.
- R represents an OH group and R 2 represents a methoxy group.
- R 3 and R 4 according to formulas (Cl) and (CM) independently of one another represent a (C 1 to C 4) -alkyl group.
- (C 1 to C 4) -alkyl group is a methyl, ethyl, n-propyl , Isopropyl, n-butyl, isobutyl or 2-methylpropyl, sec-butyl or 1-methylpropyl or a tert-butyl group to understand.
- R 3 and R 4 according to formulas (Cl) and (CM) are independently selected from a methyl, ethyl, n-propyl, isopropyl and an n-butyl group.
- R 3 and R 4 according to formulas (Cl) and (CM) independently of one another represent a methyl or ethyl group. It is extremely preferred that R 3 and R 4 are identical.
- Particularly preferred according to the invention are the 6,7-disubstituted 2,2-dialkylchromans.
- An extremely highly preferred active ingredient according to the invention is 2,2-dimethyl-6-hydroxy-7-methoxychroman with the systematic name 3,4-dihydro-7-methoxy-2,2-dimethyl-2H-1-benzopyran-6 ol and the INCI name dimethylmethoxy chromanol.
- the substance is sold under the trade name Lipochroman-6 by Lipotec S.A. available.
- the 6,7-disubstituted 2,2-dialkylchromans or chromenes of the general formulas (Cl) or (CM) are preferably used according to the invention in amounts of 0.001-0.2% by weight, preferably 0.005-0.1% by weight. , in each case based on the total weight of the agent used.
- a second subject of the invention is the use of a cosmetic agent of the first subject of the invention as a skin cosmetic.
- the cosmetic agents according to the invention of the first subject of the invention as a skin cosmetic for the care and / or protection of the skin from drying out.
- a third subject of the invention is a method in which a cosmetic agent of the first subject of the invention is applied to the skin and left on it, in particular for at least one hour.
- Cosmetic composition containing in each case based on the total weight of the composition, liquid oils in a total amount of 80 to 99.5 wt .-%, (in particular from 85 to 99 wt .-%, in particular from 90 to 98 wt .-%) , characterized in that as liquid oils
- a cosmetic composition according to item 1 characterized in that it min as a liquid oil having a spreading value (25 ° C) in a range of 100 mm 2/10 to less than 800 mm 2/10 min, at least one liquid compound of the general formula ( I),
- R is a C2 to Oo hydrocarbon group, in particular octyl
- R 2 is a C4 to Ci2 hydrocarbon group.
- Cosmetic composition according to any of the preceding points characterized in that as a liquid oil having a spreading value (25 ° C) in a range of 100 mm 2/10 min to less than 800 mm 2/10 min, at least one liquid compound of the general formula ( II) contains,
- R 3 is a C 10 to C 16 hydrocarbon group, in particular C 12 to C 15 hydrocarbon group.
- R 4 is an alkyl group having 2 to 4 carbon atoms, in particular ethyl
- R 5 is an alkyl group having 4 to 6 carbon atoms
- R 6 is an alkyl group having 7 to 17 carbon atoms.
- Cosmetic composition according to any of the preceding points characterized in that as a liquid oil having a spreading value (25 ° C) in a range of 800 mm 2/10 min to below 1050 mm 2/10 min, at least one ester of isopropanol with a C16 to C2o fatty acid contains cosmetic composition according to any one of the preceding points, characterized in that as a liquid oil having a spreading value (25 ° C) in a range of 1050 mm 2/10 minutes to 1800 mm 2/10 minutes at least one compound of the formula (IV)
- R 7 and R 8 independently represent a linear or branched alkyl group having 6 to 10 carbon atoms, in particular a linear or branched alkyl group having 8 carbon atoms.
- Cosmetic composition according to any of the preceding points characterized in that as a liquid oil having a spreading value (25 ° C) in a range of 1050 mm 2/10 minutes to 1800 mm 2/10 min, at least one ester of a (C4-C6 ) -Alkanol with a C16 to C20 fatty acid, in particular hexyl laurate contains.
- Cosmetic composition according to any of the preceding points characterized in that liquid oil having a spreading value (25 ° C) min in a range of 100 mm 2/10 to less than 800 mm 2/10 min, in a total amount from 32 to 42 parts by weight % is included.
- Cosmetic composition according to any of the preceding points characterized in that liquid oil having a spreading value (25 ° C) min in a range of 800 mm 2/10 to below 1050 mm 2/10 min, in a total amount of 35 to 50 parts by weight % is included.
- Cosmetic composition according to any of the preceding points characterized in that liquid oil having a spreading value (25 ° C) min in a range of 1050 mm 2 / 10-1800 mm 2/10 min, in a total amount of 12 to 22 wt .-% is included.
- Cosmetic composition according to one of the preceding points characterized in that the total amount of the oils mentioned under (b) to the sum of the respective total amounts of the oils mentioned under (a) and (c) in the range of 1.5 to 1 to 1 to 2, preferably between 1.2 to 1 and 1 to 1.8, more preferably between 1 to 1.2 to 1 to 1 .7.
- Cosmetic composition according to one of the preceding points characterized in that it additionally contains at least one fatty acid ester of at least one linear or branched C 6 to C 18 fatty acid with ascorbic acid. Cosmetic composition according to one of the preceding points, characterized in that it additionally contains a carotenoid, in particular ⁇ -carotene. Cosmetic composition according to one of the preceding points, characterized in that it is transparent. Cosmetic composition according to item 14, characterized in that it additionally contains 2,2-dimethyl-6-hydroxy-7-methoxy-chroman. Cosmetic composition according to one of the preceding points, characterized in that it contains 0 to 0.1% by weight of free water.
- Use of a cosmetic agent according to any one of items 1 to 16 as a skin cosmetic. Use according to item 17, characterized in that the skin cosmetic protects the skin from drying out. Method in which a cosmetic agent of points 1 to 16 is applied to the skin and left on it, in particular for at least one hour.
- the Spreitagonist were determined according to the method of the patent specification at 25 ° C. 2.0 consumer test
- formulation E1 from Table 1 a dermatological use test was carried out on 50 test persons.
- the subjects used recipe E1 for a period of 4 weeks in the morning and evening to care for the facial skin. At the end the subjects were interviewed.
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- Birds (AREA)
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Abstract
Description
Claims
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE201310217316 DE102013217316A1 (de) | 2013-08-30 | 2013-08-30 | Hautpflegeöl |
| PCT/DE2014/200336 WO2015028009A1 (de) | 2013-08-30 | 2014-07-21 | Hautpflegeöl |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| EP3038714A1 true EP3038714A1 (de) | 2016-07-06 |
Family
ID=51453546
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EP14758078.1A Ceased EP3038714A1 (de) | 2013-08-30 | 2014-07-21 | Hautpflegeöl |
Country Status (4)
| Country | Link |
|---|---|
| US (1) | US9730873B2 (de) |
| EP (1) | EP3038714A1 (de) |
| DE (1) | DE102013217316A1 (de) |
| WO (1) | WO2015028009A1 (de) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE102015205477A1 (de) | 2015-03-26 | 2016-09-29 | Henkel Ag & Co. Kgaa | "Kosmetische Zubereitungen mit geringer Textilanhaftung" |
| DE102017220988A1 (de) | 2017-11-23 | 2019-05-23 | Henkel Ag & Co. Kgaa | Kosmetische Zusammensetzungen mit reduziertem öligen oder fettigen Hautgefühl |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE19713793A1 (de) * | 1997-04-03 | 1998-10-08 | Henkel Kgaa | Öl-in-Wasser-Emulsionen zur Wiederherstellung der Lamellarität der Lipidstruktur geschädigter Haut |
| DE10062610A1 (de) | 2000-12-15 | 2002-06-27 | Merz & Co Gmbh & Co | Vesikelbildende Hautöle aus öllöslichen Komponenten und W/O-Emulgatoren nit einem HLB-Wert von 2-6 und vesikelbildenden Lipiden sowie wahlweise einem oder mehreren üblichen Zusatzstoffen, Verfahren zu deren Herstellung und ihre Verwendung |
| DE10202312A1 (de) | 2002-01-23 | 2003-07-31 | Beiersdorf Ag | Kosmetische und dermatologische Pflegeöle mit einem Gehalt an Wachsen |
| DE10361568A1 (de) * | 2003-12-23 | 2005-07-28 | Beiersdorf Ag | Kosmetische Zubereitung mit sehr guten sensorischen Eigenschaften |
| DE102005003708B4 (de) * | 2005-01-20 | 2017-11-09 | Beiersdorf Ag | Verwendung von Hautpflegeöl mit Kakaobutter |
| FR2886840B1 (fr) * | 2005-06-10 | 2007-07-20 | Oreal | Composition cosmetique anhydre contenant un polyrotaxane reticule et une huile |
| DE102006035042A1 (de) * | 2006-07-28 | 2008-01-31 | Beiersdorf Ag | Kosmetische Zubereitung |
| DE102012002951A1 (de) | 2012-02-16 | 2013-08-22 | Beiersdorf Ag | Stabile Wasser in Öl Emulsionen mit spreitfähigen Ölen |
-
2013
- 2013-08-30 DE DE201310217316 patent/DE102013217316A1/de not_active Withdrawn
-
2014
- 2014-07-21 EP EP14758078.1A patent/EP3038714A1/de not_active Ceased
- 2014-07-21 WO PCT/DE2014/200336 patent/WO2015028009A1/de not_active Ceased
-
2016
- 2016-02-17 US US15/045,361 patent/US9730873B2/en active Active
Non-Patent Citations (2)
| Title |
|---|
| None * |
| See also references of WO2015028009A1 * |
Also Published As
| Publication number | Publication date |
|---|---|
| US20160158127A1 (en) | 2016-06-09 |
| US9730873B2 (en) | 2017-08-15 |
| WO2015028009A1 (de) | 2015-03-05 |
| DE102013217316A1 (de) | 2015-03-05 |
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