ES2561160T3 - Preparaciones cosméticas que contienen ésteres a base de 2-butiloctanol - Google Patents
Preparaciones cosméticas que contienen ésteres a base de 2-butiloctanol Download PDFInfo
- Publication number
- ES2561160T3 ES2561160T3 ES07786631.7T ES07786631T ES2561160T3 ES 2561160 T3 ES2561160 T3 ES 2561160T3 ES 07786631 T ES07786631 T ES 07786631T ES 2561160 T3 ES2561160 T3 ES 2561160T3
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- ES
- Spain
- Prior art keywords
- butyloctanol
- butyl
- preparations containing
- cosmetic preparations
- butyloctyl
- 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.)
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- XMVBHZBLHNOQON-UHFFFAOYSA-N 2-butyl-1-octanol Chemical compound CCCCCCC(CO)CCCC XMVBHZBLHNOQON-UHFFFAOYSA-N 0.000 title abstract description 5
- 239000002537 cosmetic Substances 0.000 title abstract description 5
- 150000002148 esters Chemical class 0.000 title description 4
- 238000002360 preparation method Methods 0.000 title description 2
- 239000000825 pharmaceutical preparation Substances 0.000 abstract description 2
- BJMMJWWRCOVZJM-UHFFFAOYSA-N 2-butyloctyl 2-butyldecanoate Chemical compound CCCCCCCCC(CCCC)C(=O)OCC(CCCC)CCCCCC BJMMJWWRCOVZJM-UHFFFAOYSA-N 0.000 abstract 1
- ZPGSXEKHMWBPPO-UHFFFAOYSA-N 2-butyloctyl 2-butyloctanoate Chemical compound CCCCCCC(CCCC)COC(=O)C(CCCC)CCCCCC ZPGSXEKHMWBPPO-UHFFFAOYSA-N 0.000 abstract 1
- HQEKCIFEAWMJHK-UHFFFAOYSA-N 2-butyloctyl 2-hexyldecanoate Chemical compound CCCCCCCCC(CCCCCC)C(=O)OCC(CCCC)CCCCCC HQEKCIFEAWMJHK-UHFFFAOYSA-N 0.000 abstract 1
- RGCASHYLRJJOOW-UHFFFAOYSA-N 2-butyloctyl 2-octyldodecanoate Chemical compound CCCCCCCCCCC(CCCCCCCC)C(=O)OCC(CCCC)CCCCCC RGCASHYLRJJOOW-UHFFFAOYSA-N 0.000 abstract 1
- 125000002015 acyclic group Chemical group 0.000 abstract 1
- 150000001735 carboxylic acids Chemical class 0.000 abstract 1
- 150000001991 dicarboxylic acids Chemical class 0.000 abstract 1
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 12
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 10
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 9
- 238000004140 cleaning Methods 0.000 description 7
- -1 alkylene glycol esters Chemical class 0.000 description 6
- 125000004432 carbon atom Chemical group C* 0.000 description 6
- 235000011187 glycerol Nutrition 0.000 description 6
- 239000000203 mixture Substances 0.000 description 6
- QQPDTPVPANPTSO-UHFFFAOYSA-N 2-butyloctyl butanoate Chemical compound CCCCCCC(CCCC)COC(=O)CCC QQPDTPVPANPTSO-UHFFFAOYSA-N 0.000 description 5
- 239000003921 oil Substances 0.000 description 5
- 229920005862 polyol Polymers 0.000 description 5
- TUGMBKHXNILKOS-UHFFFAOYSA-N 2-butyloctyl hexanoate Chemical compound CCCCCCC(CCCC)COC(=O)CCCCC TUGMBKHXNILKOS-UHFFFAOYSA-N 0.000 description 4
- 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 4
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 4
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 4
- 239000000839 emulsion Substances 0.000 description 4
- 239000004615 ingredient Substances 0.000 description 4
- 150000003077 polyols Chemical class 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 3
- 235000014113 dietary fatty acids Nutrition 0.000 description 3
- 229930195729 fatty acid Natural products 0.000 description 3
- 239000000194 fatty acid Substances 0.000 description 3
- 150000004665 fatty acids Chemical class 0.000 description 3
- 150000002191 fatty alcohols Chemical class 0.000 description 3
- 229930182470 glycoside Natural products 0.000 description 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 3
- IIZPXYDJLKNOIY-JXPKJXOSSA-N 1-palmitoyl-2-arachidonoyl-sn-glycero-3-phosphocholine Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@H](COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCC\C=C/C\C=C/C\C=C/C\C=C/CCCCC IIZPXYDJLKNOIY-JXPKJXOSSA-N 0.000 description 2
- FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Chemical compound CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 description 2
- 239000004166 Lanolin Substances 0.000 description 2
- XUMBMVFBXHLACL-UHFFFAOYSA-N Melanin Chemical compound O=C1C(=O)C(C2=CNC3=C(C(C(=O)C4=C32)=O)C)=C2C4=CNC2=C1C XUMBMVFBXHLACL-UHFFFAOYSA-N 0.000 description 2
- 229920002125 Sokalan® Polymers 0.000 description 2
- 235000021355 Stearic acid Nutrition 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- RXKJFZQQPQGTFL-UHFFFAOYSA-N dihydroxyacetone Chemical compound OCC(=O)CO RXKJFZQQPQGTFL-UHFFFAOYSA-N 0.000 description 2
- UKMSUNONTOPOIO-UHFFFAOYSA-N docosanoic acid Chemical compound CCCCCCCCCCCCCCCCCCCCCC(O)=O UKMSUNONTOPOIO-UHFFFAOYSA-N 0.000 description 2
- 235000013399 edible fruits Nutrition 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- BJRNKVDFDLYUGJ-RMPHRYRLSA-N hydroquinone O-beta-D-glucopyranoside Chemical compound O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@H]1OC1=CC=C(O)C=C1 BJRNKVDFDLYUGJ-RMPHRYRLSA-N 0.000 description 2
- 150000002576 ketones Chemical class 0.000 description 2
- 229940039717 lanolin Drugs 0.000 description 2
- 235000019388 lanolin Nutrition 0.000 description 2
- 235000010445 lecithin Nutrition 0.000 description 2
- 239000000787 lecithin Substances 0.000 description 2
- 229940067606 lecithin Drugs 0.000 description 2
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 2
- 235000019341 magnesium sulphate Nutrition 0.000 description 2
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 2
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 2
- 239000008117 stearic acid Substances 0.000 description 2
- VARQGBHBYZTYLJ-UHFFFAOYSA-N tricosan-12-one Chemical compound CCCCCCCCCCCC(=O)CCCCCCCCCCC VARQGBHBYZTYLJ-UHFFFAOYSA-N 0.000 description 2
- KSEBMYQBYZTDHS-HWKANZROSA-M (E)-Ferulic acid Natural products COC1=CC(\C=C\C([O-])=O)=CC=C1O KSEBMYQBYZTDHS-HWKANZROSA-M 0.000 description 1
- NGCDGPPKVSZGRR-UHFFFAOYSA-J 1,4,6,9-tetraoxa-5-stannaspiro[4.4]nonane-2,3,7,8-tetrone Chemical compound [Sn+4].[O-]C(=O)C([O-])=O.[O-]C(=O)C([O-])=O NGCDGPPKVSZGRR-UHFFFAOYSA-J 0.000 description 1
- HBXWUCXDUUJDRB-UHFFFAOYSA-N 1-octadecoxyoctadecane Chemical compound CCCCCCCCCCCCCCCCCCOCCCCCCCCCCCCCCCCCC HBXWUCXDUUJDRB-UHFFFAOYSA-N 0.000 description 1
- ULQISTXYYBZJSJ-UHFFFAOYSA-N 12-hydroxyoctadecanoic acid Chemical compound CCCCCCC(O)CCCCCCCCCCC(O)=O ULQISTXYYBZJSJ-UHFFFAOYSA-N 0.000 description 1
- KIHBGTRZFAVZRV-UHFFFAOYSA-N 2-Hydroxyoctadecanoic acid Natural products CCCCCCCCCCCCCCCCC(O)C(O)=O KIHBGTRZFAVZRV-UHFFFAOYSA-N 0.000 description 1
- RFVNOJDQRGSOEL-UHFFFAOYSA-N 2-hydroxyethyl octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCCO RFVNOJDQRGSOEL-UHFFFAOYSA-N 0.000 description 1
- QCDWFXQBSFUVSP-UHFFFAOYSA-N 2-phenoxyethanol Chemical compound OCCOC1=CC=CC=C1 QCDWFXQBSFUVSP-UHFFFAOYSA-N 0.000 description 1
- FJKROLUGYXJWQN-UHFFFAOYSA-N 4-hydroxybenzoic acid Chemical compound OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 1
- 235000021357 Behenic acid Nutrition 0.000 description 1
- 241001090476 Castoreum Species 0.000 description 1
- 235000013162 Cocos nucifera Nutrition 0.000 description 1
- 244000060011 Cocos nucifera Species 0.000 description 1
- ZZZCUOFIHGPKAK-UHFFFAOYSA-N D-erythro-ascorbic acid Natural products OCC1OC(=O)C(O)=C1O ZZZCUOFIHGPKAK-UHFFFAOYSA-N 0.000 description 1
- 241000282375 Herpestidae Species 0.000 description 1
- OUYCCCASQSFEME-QMMMGPOBSA-N L-tyrosine Chemical compound OC(=O)[C@@H](N)CC1=CC=C(O)C=C1 OUYCCCASQSFEME-QMMMGPOBSA-N 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- 235000010654 Melissa officinalis Nutrition 0.000 description 1
- 244000062730 Melissa officinalis Species 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- 241000209504 Poaceae Species 0.000 description 1
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 description 1
- 229930003268 Vitamin C Natural products 0.000 description 1
- 125000002252 acyl group Chemical group 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000001299 aldehydes Chemical class 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- 230000003712 anti-aging effect Effects 0.000 description 1
- 230000001166 anti-perspirative effect Effects 0.000 description 1
- 239000003213 antiperspirant Substances 0.000 description 1
- 229960000271 arbutin Drugs 0.000 description 1
- 235000010323 ascorbic acid Nutrition 0.000 description 1
- 239000011668 ascorbic acid Substances 0.000 description 1
- 229960005070 ascorbic acid Drugs 0.000 description 1
- OGBUMNBNEWYMNJ-UHFFFAOYSA-N batilol Chemical class CCCCCCCCCCCCCCCCCCOCC(O)CO OGBUMNBNEWYMNJ-UHFFFAOYSA-N 0.000 description 1
- 229940116226 behenic acid Drugs 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 150000001733 carboxylic acid esters Chemical class 0.000 description 1
- 229940073669 ceteareth 20 Drugs 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 230000035614 depigmentation Effects 0.000 description 1
- 229940120503 dihydroxyacetone Drugs 0.000 description 1
- 229940085632 distearyl ether Drugs 0.000 description 1
- 230000032050 esterification Effects 0.000 description 1
- 238000005886 esterification reaction Methods 0.000 description 1
- BEFDCLMNVWHSGT-UHFFFAOYSA-N ethenylcyclopentane Chemical compound C=CC1CCCC1 BEFDCLMNVWHSGT-UHFFFAOYSA-N 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 description 1
- 239000000284 extract Substances 0.000 description 1
- 230000001815 facial effect Effects 0.000 description 1
- 150000002192 fatty aldehydes Chemical class 0.000 description 1
- 150000002195 fatty ethers Chemical class 0.000 description 1
- KSEBMYQBYZTDHS-HWKANZROSA-N ferulic acid Chemical compound COC1=CC(\C=C\C(O)=O)=CC=C1O KSEBMYQBYZTDHS-HWKANZROSA-N 0.000 description 1
- 229940114124 ferulic acid Drugs 0.000 description 1
- KSEBMYQBYZTDHS-UHFFFAOYSA-N ferulic acid Natural products COC1=CC(C=CC(O)=O)=CC=C1O KSEBMYQBYZTDHS-UHFFFAOYSA-N 0.000 description 1
- 235000001785 ferulic acid Nutrition 0.000 description 1
- 239000004872 foam stabilizing agent Substances 0.000 description 1
- 239000008098 formaldehyde solution Substances 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 125000005456 glyceride group Chemical group 0.000 description 1
- 150000002338 glycosides Chemical class 0.000 description 1
- 235000008216 herbs Nutrition 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 239000003752 hydrotrope Substances 0.000 description 1
- 238000005470 impregnation Methods 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 239000000077 insect repellent Substances 0.000 description 1
- 239000000865 liniment Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
- BJRNKVDFDLYUGJ-UHFFFAOYSA-N p-hydroxyphenyl beta-D-alloside Natural products OC1C(O)C(O)C(CO)OC1OC1=CC=C(O)C=C1 BJRNKVDFDLYUGJ-UHFFFAOYSA-N 0.000 description 1
- UWJJYHHHVWZFEP-UHFFFAOYSA-N pentane-1,1-diol Chemical compound CCCCC(O)O UWJJYHHHVWZFEP-UHFFFAOYSA-N 0.000 description 1
- 229960005323 phenoxyethanol Drugs 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 238000007142 ring opening reaction Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 235000010199 sorbic acid Nutrition 0.000 description 1
- 239000004334 sorbic acid Substances 0.000 description 1
- 229940075582 sorbic acid Drugs 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 230000036561 sun exposure Effects 0.000 description 1
- 230000000475 sunscreen effect Effects 0.000 description 1
- 239000000516 sunscreening agent Substances 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
- QURCVMIEKCOAJU-UHFFFAOYSA-N trans-isoferulic acid Natural products COC1=CC=C(C=CC(O)=O)C=C1O QURCVMIEKCOAJU-UHFFFAOYSA-N 0.000 description 1
- OUYCCCASQSFEME-UHFFFAOYSA-N tyrosine Natural products OC(=O)C(N)CC1=CC=C(O)C=C1 OUYCCCASQSFEME-UHFFFAOYSA-N 0.000 description 1
- 235000019154 vitamin C Nutrition 0.000 description 1
- 239000011718 vitamin C Substances 0.000 description 1
- 239000000341 volatile oil Substances 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
- 239000002023 wood Substances 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
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
- C07C69/02—Esters of acyclic saturated monocarboxylic acids having the carboxyl group bound to an acyclic carbon atom or to hydrogen
- C07C69/22—Esters of acyclic saturated monocarboxylic acids having the carboxyl group bound to an acyclic carbon atom or to hydrogen having three or more carbon atoms in the acid moiety
- C07C69/24—Esters of acyclic saturated monocarboxylic acids having the carboxyl group bound to an acyclic carbon atom or to hydrogen having three or more carbon atoms in the acid moiety esterified with monohydroxylic compounds
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/21—Esters, e.g. nitroglycerine, selenocyanates
- A61K31/215—Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids
- A61K31/22—Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids of acyclic acids, e.g. pravastatin
- A61K31/23—Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids of acyclic acids, e.g. pravastatin of acids having a carboxyl group bound to a chain of seven or more carbon atoms
-
- 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
- A61K8/0208—Tissues; Wipes; Patches
-
- 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
- A61K8/92—Oils, fats or waxes; Derivatives thereof, e.g. hydrogenation products thereof
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
- C07C69/003—Esters of saturated alcohols having the esterified hydroxy group bound to an acyclic carbon atom
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q5/00—Preparations for care of the hair
- A61Q5/12—Preparations containing hair conditioners
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Epidemiology (AREA)
- Birds (AREA)
- Emergency Medicine (AREA)
- Dermatology (AREA)
- Engineering & Computer Science (AREA)
- Biomedical Technology (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Cosmetics (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Medicinal Preparation (AREA)
Abstract
Empleo de ésteres del 2-butil-1-octanol con ácidos carboxílicos C2-C36 acíclicos - o ácidos dicarboxílicos C6-C36 lineales no ramificados en preparaciones cosméticas y/o farmacéuticas con excepción de 2-butiloctil-2- butiloctanoato, 2-butiloctil-2-butildecanoato, 2-butiloctil-2-hexildecanoato, 2-butiloctil-2-octildodecanoato.
Description
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Como autobronceador es adecuada dihidroxiacetona. Como inhibidores de tirosina, que impiden la formación de melanina y encuentran aplicación en agentes de despigmentación, entran en consideración por ejemplo arbutina, ácido ferúlico, ácido cójico, ácido cumárico y ácido ascórbico (vitamina C).
Como agentes conservantes son adecuados por ejemplo fenoxietanol, solución de formaldehído, parabeno, pentanodiol o ácido sórbico así como los complejos de plata conocidos bajo la denominación Surfacine® y las otras clases de sustancias citadas en el anexo 6, partes A y B de la regulación de cosméticos.
Como aceites esenciales se mencionan mezclas de sustancias odoríferas naturales y sintéticas. Las sustancias odoríferas naturales son extractos de flores, tallos y hojas, frutas, cáscaras de frutas, raíces, maderas, hierbas y pastos, agujas y ramas, resinas y bálsamos. Además, entran en consideración materias primas animales, como por ejemplo civeto y castoreum así como compuestos odoríferos sintéticos del tipo de los ésteres, éteres, aldehídos, cetonas, alcoholes e hidrocarburos.
Como ceras de brillo perlino, en particular para el uso en formulaciones surfactantes entran en consideración por ejemplo: alquilenglicolésteres, especialmente etilenglicoldiestearato; alcanolamidas grasas, especialmente dietanolamida de coco; glicéridos parciales, especialmente monoglicéridos de ácido esteárico; ésteres de ácidos carboxílicos polivalentes, dado el caso sustituidos con hidroxilo con alcoholes grasos con 6 a 22 átomos de carbono, especialmente ésteres de cadena larga del ácido tartárico; sólidos, como por ejemplo alcoholes grasos, cetonas grasas, aldehídos grasos, éteres grasos y carbonatos grasos, que en total exhiben al menos 24 átomos de carbono, especialmente laurona y diesteariléter; ácidos grasos como ácido esteárico, ácido hidroxiesteárico o ácido behénico, productos de apertura de anillo de epóxidos de olefina con 12 a 22 átomos de carbono con alcoholes grasos con 12 a 22 átomos de carbono y/o polioles con 2 a 15 átomos de carbono y 2 a 10 grupos hidroxilo así como sus mezclas.
Como agentes sobreengrasantes pueden usarse sustancias como por ejemplo lanolina y lecitina así como derivados de lanolina y lecitina con varios grupos etoxilo o grupo acilo, ésteres de poliol y ácidos grasos, monoglicéridos y alcanolamidas grasas, en donde las últimas sirven simultáneamente como estabilizadores de espuma.
Como estabilizantes pueden emplearse sales metálicas de ácidos grasos, como por ejemplo estearato o bien ricinoleato de magnesio, aluminio y/o zinc.
Para el mejoramiento del comportamiento de fluidez pueden emplearse además hidrotropos, como por ejemplo etanol, isopropilalcohol, o polioles. Los polioles que entran aquí en consideración poseen preferiblemente 2 a 15 átomos de carbono y al menos dos grupos hidroxilo. Los polioles pueden contener aún otros grupos funcionales, en particular grupos amino o bien pueden estar modificados con nitrógeno.
Las preparaciones de acuerdo con la invención, las composiciones de acuerdo con la invención así como los ésteres según la invención son adecuados en particular en preparaciones cosméticas y/o farmacéuticas para la humectación
o impregnación o recubrimiento de paños personales y de higiene, que se usan para la limpieza corporal y/o para cuidado corporal.
Como paños personales y de higiene se mencionan a modo de ejemplo: pañuelos, papeles, limpiones, productos de fieltro, esponjas, aplicadores faciales, esparadrapo y vendajes, que encuentran su uso en el campo de la higiene y el cuidado. Estos pueden ser paños húmedos para la higiene del bebé y el cuidado del bebé, paños para limpieza, paños para limpieza de la cara, paños para el cuidado de la piel, paños para el cuidado con principios activos contra el envejecimiento de la piel, limpiones con formulaciones protectoras contra el sol y repelentes contra insectos así como limpiones para los cosméticos decorativos o para el tratamiento después de la exposición al sol, paños húmedos de baño, limpiones antitranspirantes, pañales, paños de bolsillo, limpiones húmedos, productos de higiene así como limpiones de autobronceado.
Ejemplos
Ejemplo 1: producción de octilbutanoato de 2-butilo por medio de esterificación
Se calentaron 344 g de ácido butírico (3,9 mol) y 852 g de Isofol 12 (butiloctanol) (4,7 mol) junto con 0,6 g de Fascat® 2001 (oxalato de estaño: 0,1 % % en peso referido a la composición total) 5 h a 240 °C en el separador de agua. Después de terminar la separación de agua, se separó por destilación primero el exceso de butiloctanol y a continuación se destiló al vacío el producto en el producto (139°C a 3 mbar). El producto surgió como un aceite delgado incoloro.
Recetas
16
Tabla 1: Emulsiones aceite en agua
- Ingrediente Nombre comercial (INCI)
- 1 2 3 4 5
- Emulgade® PL 68/50 (Cetearil glucósidos, Cetearil alcohol)
- 4,50 4,50 4,50
- Eumulgin® VL75 (Lauril glucósidos, Poligliceril -2 dipolihidroxiestearato, glicerina)
- 4,50 4,50
- Octilbutanoato de 2-butilo
- 14,00 16,00 16,00
- Octilhexanoato de 2-butilo
- 16,00 12,00
- Carbopol® 980
- 0,30 0,30
- Lanette® O
- KOH (al 20%)
- 0,70 0,70
- Glicerina al 99,5%
- 3,00 3,00 3,00 3,00 3,00
- Solución de formol, al 37%
- 0,15 0,15 0,15 0,15 0,15
- Agua dest.
- hasta 100 hasta 100 hasta 100 hasta 100 hasta 100
Tabla 2: Emulsiones aceite en agua
- Ingrediente: Nombre comercial (INCI)
- 6 7 8 9
- Eumulgin® VL75 (Lauril glucósidos, Poligliceril -2 Dipolihidroxiestearato, Glicerina)
- 4,50
- Eumulgin ®B2 (Ceteareth-20)
- 2,00 2,00 2,00
- Octilbutanoato de 2-butilo
- 14,00 16,00
- Octilhexanoato de 2-butilo
- 16,00 16,00
- Carbopol® 980
- 0,30 0,30
- Lanette® O
- 5,00 5,00 5,00
- KOH (al 20%)
- 0,70
- Glicerina al 99,5%
- 3,00 3,00 3,00 3,00
- Solución de formol al 37%
- 0,15 0,15 0,15 0,15
- Agua dest.
- hasta 100 hasta 100 hasta 100 hasta 100
- Valor de pH
- 6,70 7,10 5,70 6,80
17
Tabla 3: Emulsiones agua en aceite
- Ingrediente: Nombre comercial (INCI)
- 10 11 12 13 14 15
- Dehymuls ®LE (PEG-30-Dipolihidroxiestearato)
- 5,00 5,00 5,00
- Dehymuls® PGPH (Poligliceril-2-Dipolihidroxiestearato)
- 4,00 4,00 4,00
- Lameform ®TGI (Poligliceril-3-Diisoestearato)
- 2,00 2,00 2,00
- Octilbutanoato de 2-butilo
- 20,00 18,00 20,00 18,00
- Octilhexanoato de 2-butilo
- 20,00 20,00
- MgSO4*7H2O
- 1,00 1,00 1,00 1,00 1,00 1,00
- Glicerina al 99,5%
- 5,00 5,00 5,00 5,00 5,00 5,00
- Solución de formol al 37%
- 0,15 0,15 0,15 0,15 0,15 0,15
- Agua dest.
- hasta 100 hasta 100 hasta 100 hasta 100 hasta 100 hasta 100
Tabla 4: Emulsiones agua en aceite
- Ingrediente: Nombre comercial (INCI)
- 16 17 18
- Dehymuls ®LE (PEG-30-Dipolihidroxiestearato)
- 4,00 4,00 4,00
- Lameform ®TGI (Poligliceril-3-diisoestearato)
- 2,00 2,00 2,00
- Octilbutanoato de 2-butilo
- 20,00
- Octilhexanoato de 2-butilo
- 20,00 15,00
- MgSO4*7H2O
- 1,00 1,00 1,00
- Glicerina al 99,5%
- 5,00 5,00 5,00
- Solución de formol al 37%
- 0,15 0,15 0,15
- Agua dest.
- hasta 100 hasta 100 hasta 100
18
20
21
Claims (1)
-
imagen1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP06017217 | 2006-08-18 | ||
| EP06017217A EP1889640A1 (de) | 2006-08-18 | 2006-08-18 | Kosmetische Zusammensetzungen enthaltend Ester auf Basis von 2-Butyl-1-octanol |
| PCT/EP2007/007037 WO2008019794A1 (de) | 2006-08-18 | 2007-08-09 | Kosmetische zusammensetzungen enthaltend ester auf basis von 2-butyl-octanol |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| ES2561160T3 true ES2561160T3 (es) | 2016-02-24 |
| ES2561160T5 ES2561160T5 (es) | 2018-09-19 |
Family
ID=37671349
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES07786631.7T Active ES2561160T5 (es) | 2006-08-18 | 2007-08-09 | Preparaciones cosméticas que contienen ésteres a base de 2-butiloctanol |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US20100298432A1 (es) |
| EP (2) | EP1889640A1 (es) |
| JP (1) | JP5563820B2 (es) |
| KR (1) | KR101446815B1 (es) |
| CN (1) | CN101505833B (es) |
| ES (1) | ES2561160T5 (es) |
| WO (1) | WO2008019794A1 (es) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP1889640A1 (de) | 2006-08-18 | 2008-02-20 | Cognis IP Management GmbH | Kosmetische Zusammensetzungen enthaltend Ester auf Basis von 2-Butyl-1-octanol |
| EP1985281A1 (de) * | 2007-04-26 | 2008-10-29 | Cognis IP Management GmbH | Ester von Hexyldecanol mit kurzkettigen Fettsäuren |
| EP1990041A1 (de) * | 2007-05-07 | 2008-11-12 | Cognis IP Management GmbH | Kosmetische Zusammensetzungen enthaltend Ester auf Basis von 2-Propylheptansäure |
| EP3107890A4 (en) * | 2014-02-18 | 2017-07-05 | Elevance Renewable Sciences, Inc. | Branched-chain esters and methods of making and using the same |
| WO2017025647A1 (en) * | 2015-08-13 | 2017-02-16 | Arch Personal Care Products, Lp | Wet wipe concentrate |
| EP3178907A1 (en) * | 2015-12-09 | 2017-06-14 | Basf Se | The use of isostearic acid esters as lubricants |
Family Cites Families (25)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2014310A (en) * | 1934-05-11 | 1935-09-10 | Carbide & Carbon Chem Corp | Esters of 2-butyloctanol |
| DE1594388A1 (de) * | 1964-08-27 | 1970-04-09 | Deutsche Erdoel Ag | Schmier- und Industrieoele |
| JPS576790A (en) * | 1980-06-13 | 1982-01-13 | Canon Inc | Recording liquid and recording method |
| DE4202034A1 (de) * | 1992-01-25 | 1993-07-29 | Rwe Dea Ag | Hydraulikfluessigkeiten |
| DE4341794C1 (de) * | 1993-12-08 | 1995-01-19 | Henkel Kgaa | Kosmetische und/oder pharmazeutische Zubereitungen mit verbessertem Hautgefühl |
| DE4420516C2 (de) * | 1994-06-13 | 1998-10-22 | Henkel Kgaa | Polyglycerinpolyhydroxystearate |
| US5849273A (en) | 1996-11-21 | 1998-12-15 | The C. P. Hall Company | Skin care and sunscreen composition containing dibenzoylmethane derivative, e.g., parsol® 1789, and C12, C16, C18 branched chain hydroxybenzoate and/or C12, C16 branched chain benzoate stabilizers/solubilizers |
| DE19742275A1 (de) * | 1997-09-25 | 1999-04-01 | Beiersdorf Ag | Estern verzweigtkettiger Carbonsäuren und verzweigtkettiger Alkohole als antibakterielle, antimycotische, antiparasitäre oder antivirale Wirkstoffe |
| US6827220B1 (en) * | 1998-08-11 | 2004-12-07 | Versitech, Inc. | Flotation of sulfide mineral species with oils |
| DE69926537T2 (de) * | 1998-10-29 | 2006-06-08 | Penreco, Houston | Gelzusammensetzung |
| AU5764800A (en) | 1999-07-01 | 2001-01-22 | Johnson & Johnson Consumer Companies, Inc. | Cleansing compositions |
| JP2003034795A (ja) * | 2001-07-23 | 2003-02-07 | Sanyo Chem Ind Ltd | 潤滑油用基油 |
| DE10160681A1 (de) | 2001-12-11 | 2003-06-18 | Cognis Deutschland Gmbh | Emollients und kosmetische Zusammensetzungen |
| DE10160682A1 (de) * | 2001-12-11 | 2003-06-18 | Cognis Deutschland Gmbh | Emollients und kosmetische Zusammensetzungen |
| DE10162841A1 (de) | 2001-12-20 | 2003-07-03 | Beiersdorf Ag | Kosmetische und dermatologische Lichtschutzformulierungen mit einem Gehalt an Benzoxazol-Derivaten |
| US6485713B1 (en) * | 2002-03-05 | 2002-11-26 | The C. P. Hall Company | Sunscreen compositions and methods and materials for producing the same |
| DE10239712A1 (de) | 2002-08-29 | 2004-03-11 | Beiersdorf Ag | Kosmetische Zubereitung auf Basis ölhaltiger Mikroemulsionen |
| DE10317781A1 (de) * | 2003-04-16 | 2004-11-04 | Cognis Deutschland Gmbh & Co. Kg | Poly-alpha-Olefin-haltige kosmetische Zusammensetzung |
| EP1491557A1 (en) * | 2003-06-27 | 2004-12-29 | Cerestar Holding B.V. | Resistant starch compositions |
| DE10333710A1 (de) | 2003-07-23 | 2005-02-24 | Beiersdorf Ag | Kosmetische, dermatologische oder pharmazeutische Zubereitungen auf Basis von Gase enthaltenden Lipid/Wachs-Gemischen |
| US20050240040A1 (en) | 2004-04-26 | 2005-10-27 | Kendall J K | Process for producing esters employing hydrolyzable catalysts |
| DE102005025495A1 (de) * | 2005-06-01 | 2006-12-14 | Henkel Kgaa | Ölhaltige desodorierende Aerosolzusammensetzungen mit hautkühlenden Wirkstoffen |
| DE102006001768A1 (de) | 2006-01-12 | 2007-07-19 | Cognis Ip Management Gmbh | Verwendung von Estern mit verzweigten Alkylgruppen als Schmiermittel |
| EP1889640A1 (de) | 2006-08-18 | 2008-02-20 | Cognis IP Management GmbH | Kosmetische Zusammensetzungen enthaltend Ester auf Basis von 2-Butyl-1-octanol |
| EP1905419A1 (de) | 2006-09-20 | 2008-04-02 | Cognis IP Management GmbH | Kosmetische Zubereitung und Ölkörper Mischungen |
-
2006
- 2006-08-18 EP EP06017217A patent/EP1889640A1/de not_active Withdrawn
-
2007
- 2007-08-09 ES ES07786631.7T patent/ES2561160T5/es active Active
- 2007-08-09 WO PCT/EP2007/007037 patent/WO2008019794A1/de not_active Ceased
- 2007-08-09 EP EP07786631.7A patent/EP2051781B2/de active Active
- 2007-08-09 KR KR1020097003273A patent/KR101446815B1/ko active Active
- 2007-08-09 JP JP2009524932A patent/JP5563820B2/ja active Active
- 2007-08-09 CN CN200780030732.3A patent/CN101505833B/zh active Active
- 2007-08-09 US US12/377,907 patent/US20100298432A1/en not_active Abandoned
Also Published As
| Publication number | Publication date |
|---|---|
| WO2008019794A1 (de) | 2008-02-21 |
| EP2051781A1 (de) | 2009-04-29 |
| EP2051781B2 (de) | 2018-05-02 |
| JP2010501018A (ja) | 2010-01-14 |
| CN101505833B (zh) | 2014-05-21 |
| ES2561160T5 (es) | 2018-09-19 |
| JP5563820B2 (ja) | 2014-07-30 |
| CN101505833A (zh) | 2009-08-12 |
| EP2051781B1 (de) | 2015-12-02 |
| KR101446815B1 (ko) | 2014-10-02 |
| EP1889640A1 (de) | 2008-02-20 |
| US20100298432A1 (en) | 2010-11-25 |
| KR20090043521A (ko) | 2009-05-06 |
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