JP5944100B2 - 炭化水素混合物およびその使用 - Google Patents
炭化水素混合物およびその使用 Download PDFInfo
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- JP5944100B2 JP5944100B2 JP2010512573A JP2010512573A JP5944100B2 JP 5944100 B2 JP5944100 B2 JP 5944100B2 JP 2010512573 A JP2010512573 A JP 2010512573A JP 2010512573 A JP2010512573 A JP 2010512573A JP 5944100 B2 JP5944100 B2 JP 5944100B2
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- 229960003500 triclosan Drugs 0.000 description 1
- UYERRXOXXRNFHC-UHFFFAOYSA-N tridodecyl 2-hydroxypropane-1,2,3-tricarboxylate Chemical compound CCCCCCCCCCCCOC(=O)CC(O)(C(=O)OCCCCCCCCCCCC)CC(=O)OCCCCCCCCCCCC UYERRXOXXRNFHC-UHFFFAOYSA-N 0.000 description 1
- 239000001069 triethyl citrate Substances 0.000 description 1
- VMYFZRTXGLUXMZ-UHFFFAOYSA-N triethyl citrate Natural products CCOC(=O)C(O)(C(=O)OCC)C(=O)OCC VMYFZRTXGLUXMZ-UHFFFAOYSA-N 0.000 description 1
- 235000013769 triethyl citrate Nutrition 0.000 description 1
- FAGMGMRSURYROS-UHFFFAOYSA-M trihexadecyl(methyl)azanium;chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCC[N+](C)(CCCCCCCCCCCCCCCC)CCCCCCCCCCCCCCCC FAGMGMRSURYROS-UHFFFAOYSA-M 0.000 description 1
- 229940118576 triisostearyl citrate Drugs 0.000 description 1
- HTJNEBVCZXHBNJ-XCTPRCOBSA-H trimagnesium;(2r)-2-[(1s)-1,2-dihydroxyethyl]-3,4-dihydroxy-2h-furan-5-one;diphosphate Chemical compound [Mg+2].[Mg+2].[Mg+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O.OC[C@H](O)[C@H]1OC(=O)C(O)=C1O HTJNEBVCZXHBNJ-XCTPRCOBSA-H 0.000 description 1
- UZNHKBFIBYXPDV-UHFFFAOYSA-N trimethyl-[3-(2-methylprop-2-enoylamino)propyl]azanium;chloride Chemical compound [Cl-].CC(=C)C(=O)NCCC[N+](C)(C)C UZNHKBFIBYXPDV-UHFFFAOYSA-N 0.000 description 1
- OEIXGLMQZVLOQX-UHFFFAOYSA-N trimethyl-[3-(prop-2-enoylamino)propyl]azanium;chloride Chemical compound [Cl-].C[N+](C)(C)CCCNC(=O)C=C OEIXGLMQZVLOQX-UHFFFAOYSA-N 0.000 description 1
- LINXHFKHZLOLEI-UHFFFAOYSA-N trimethyl-[phenyl-bis(trimethylsilyloxy)silyl]oxysilane Chemical compound C[Si](C)(C)O[Si](O[Si](C)(C)C)(O[Si](C)(C)C)C1=CC=CC=C1 LINXHFKHZLOLEI-UHFFFAOYSA-N 0.000 description 1
- UKBHVNMEMHTWQO-UHFFFAOYSA-N trioctadecyl 2-hydroxypropane-1,2,3-tricarboxylate Chemical compound CCCCCCCCCCCCCCCCCCOC(=O)CC(O)(C(=O)OCCCCCCCCCCCCCCCCCC)CC(=O)OCCCCCCCCCCCCCCCCCC UKBHVNMEMHTWQO-UHFFFAOYSA-N 0.000 description 1
- 150000004072 triols Chemical class 0.000 description 1
- FQAZRHVERGEKOS-UHFFFAOYSA-N tripropan-2-yl 2-hydroxypropane-1,2,3-tricarboxylate Chemical compound CC(C)OC(=O)CC(O)(C(=O)OC(C)C)CC(=O)OC(C)C FQAZRHVERGEKOS-UHFFFAOYSA-N 0.000 description 1
- ODHUFJLMXDXVRC-UHFFFAOYSA-N tripropyl 2-hydroxypropane-1,2,3-tricarboxylate Chemical compound CCCOC(=O)CC(O)(C(=O)OCCC)CC(=O)OCCC ODHUFJLMXDXVRC-UHFFFAOYSA-N 0.000 description 1
- ICWQKCGSIHTZNI-UHFFFAOYSA-N tris(16-methylheptadecyl) 2-hydroxypropane-1,2,3-tricarboxylate Chemical compound CC(C)CCCCCCCCCCCCCCCOC(=O)CC(O)(C(=O)OCCCCCCCCCCCCCCCC(C)C)CC(=O)OCCCCCCCCCCCCCCCC(C)C ICWQKCGSIHTZNI-UHFFFAOYSA-N 0.000 description 1
- ZQTYRTSKQFQYPQ-UHFFFAOYSA-N trisiloxane Chemical compound [SiH3]O[SiH2]O[SiH3] ZQTYRTSKQFQYPQ-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
- 229940040064 ubiquinol Drugs 0.000 description 1
- QNTNKSLOFHEFPK-UPTCCGCDSA-N ubiquinol-10 Chemical compound COC1=C(O)C(C)=C(C\C=C(/C)CC\C=C(/C)CC\C=C(/C)CC\C=C(/C)CC\C=C(/C)CC\C=C(/C)CC\C=C(/C)CC\C=C(/C)CC\C=C(/C)CCC=C(C)C)C(O)=C1OC QNTNKSLOFHEFPK-UPTCCGCDSA-N 0.000 description 1
- 229940035936 ubiquinone Drugs 0.000 description 1
- 235000013799 ultramarine blue Nutrition 0.000 description 1
- 229940116269 uric acid Drugs 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 230000000007 visual effect Effects 0.000 description 1
- 229940088594 vitamin Drugs 0.000 description 1
- 229930003231 vitamin Natural products 0.000 description 1
- 235000013343 vitamin Nutrition 0.000 description 1
- 239000011782 vitamin Substances 0.000 description 1
- 235000019155 vitamin A Nutrition 0.000 description 1
- 239000011719 vitamin A Substances 0.000 description 1
- 229940045997 vitamin a Drugs 0.000 description 1
- 150000003722 vitamin derivatives Chemical class 0.000 description 1
- 239000000341 volatile oil Substances 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 235000019386 wax ester Nutrition 0.000 description 1
- 239000012463 white pigment Substances 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 229920001285 xanthan gum Polymers 0.000 description 1
- 239000000230 xanthan gum Substances 0.000 description 1
- 235000010493 xanthan gum Nutrition 0.000 description 1
- 229940082509 xanthan gum Drugs 0.000 description 1
- 150000003751 zinc Chemical class 0.000 description 1
- 229940071566 zinc glycinate Drugs 0.000 description 1
- XOOUIPVCVHRTMJ-UHFFFAOYSA-L zinc stearate Chemical compound [Zn+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O XOOUIPVCVHRTMJ-UHFFFAOYSA-L 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
- 229910001928 zirconium oxide Inorganic materials 0.000 description 1
- 239000004711 α-olefin Substances 0.000 description 1
- 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 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
- A61K8/31—Hydrocarbons
-
- 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
- A61K31/01—Hydrocarbons
-
- 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
- A61K8/06—Emulsions
- A61K8/062—Oil-in-water emulsions
-
- 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
- A61K8/06—Emulsions
- A61K8/064—Water-in-oil emulsions, e.g. Water-in-silicone emulsions
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q1/00—Make-up preparations; Body powders; Preparations for removing make-up
- A61Q1/02—Preparations containing skin colorants, e.g. pigments
- A61Q1/04—Preparations containing skin colorants, e.g. pigments for lips
-
- 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
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q17/00—Barrier preparations; Preparations brought into direct contact with the skin for affording protection against external influences, e.g. sunlight, X-rays or other harmful rays, corrosive materials, bacteria or insect stings
- A61Q17/04—Topical preparations for affording protection against sunlight or other radiation; Topical sun tanning preparations
-
- 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
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q19/00—Preparations for care of the skin
- A61Q19/04—Preparations for care of the skin for chemically tanning the skin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q19/00—Preparations for care of the skin
- A61Q19/10—Washing or bathing preparations
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q5/00—Preparations for care of the hair
- A61Q5/06—Preparations for styling the hair, e.g. by temporary shaping or colouring
-
- 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
- A61K2800/10—General cosmetic use
-
- 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
- A61K2800/591—Mixtures of compounds not provided for by any of the codes A61K2800/592 - A61K2800/596
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/0012—Galenical forms characterised by the site of application
- A61K9/0014—Skin, i.e. galenical aspects of topical compositions
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Dermatology (AREA)
- Epidemiology (AREA)
- Chemical & Material Sciences (AREA)
- Birds (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Dispersion Chemistry (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Cosmetics (AREA)
- Medicinal Preparation (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Emulsifying, Dispersing, Foam-Producing Or Wetting Agents (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
用語「炭素数」は、炭化水素中に存在する全ての炭素原子を包含する。したがって、例えば、ウンデカンに対しては11、トリデカンに対しては13である。
nは、好ましくは、奇数、特に7、9、11、13、15、17、19、21および/または23である。
パラメーター「炭化水素の総量」には、炭素数に関係なく、該混合物に存在する全ての炭化水素が含まれる。
14N + 1n → 14C + 1p
炭素がこのサイクルから取り除かれる(すなわち、化石になる)場合、分解する14C同位体は、新しいものには取り替わらないため、14Cと12Cとの間の比率は変化する。
本発明の炭化水素混合物は、少なくとも2つの異なる炭化水素を含有する。本発明は、少なくとも1つの炭化水素が14C同位体を含有する;好ましくは2つの異なる炭化水素が14C同位体を含有する炭化水素混合物に関する。本発明の好ましい実施態様において、炭化水素混合物中に存在する全ての炭化水素は、14C同位体を含有する。
本発明の好ましい実施態様は、炭素数が1を超えて異なる少なくとも2つの異なる炭化水素を含有し、かつ直鎖状C11および直鎖状C13炭化水素を含有する、14C同位体含有炭化水素混合物に関する。直鎖状C11炭化水素は、好ましくはn−ウンデカンである。直鎖状C13炭化水素は、好ましくはn−トリデカンである。本発明の好ましい実施態様において、本発明の炭化水素混合物は、直鎖状C11および直鎖状C13炭化水素、および、C12、C15、C16、C17、C18、C19、C20、C21およびC23炭化水素からなる群から選択される、好ましくはC15、C17、C19、C21およびC23炭化水素からなる群から選択される少なくとも1つのさらなる直鎖状炭化水素を含有する。直鎖状飽和炭化水素が好ましい。好適な直鎖状C15炭化水素は、n−ペンタデカンである;好適な直鎖状C17炭化水素は、n−ヘプタデカンである;好適な直鎖状C19炭化水素は、n−ノナデカンである。
(a)50〜90重量%の直鎖状C−11炭化水素、好ましくはn−ウンデカン
(b)10〜50重量%の直鎖状C−13炭化水素、好ましくはn−トリデカン
を含有する、14C同位体含有炭化水素混合物に関する。
(a)55〜80重量%、特に60〜75重量%、特に65〜70重量%の直鎖状C11炭化水素、好ましくはn−ウンデカン
(b)20〜45重量%、特に24〜40重量%、特に24〜30重量%の直鎖状C13炭化水素、好ましくはn−トリデカン
を含有する、14C同位体含有炭化水素混合物が特に好ましい。
本発明の好ましい実施態様は、炭素数が1を超えて異なる少なくとも2つの異なる炭化水素を含有し、かつ直鎖状C11および直鎖状C15炭化水素を含有する、14C同位体含有炭化水素混合物に関する。直鎖状C11炭化水素は、好ましくはn−ウンデカンである。直鎖状C15炭化水素は、好ましくはn−ペンタデカンである。本発明の好ましい実施態様において、本発明の炭化水素混合物は、直鎖状C11および直鎖状C15炭化水素、および、C12、C13、C14、C16、C17、C18、C19、C20、C21およびC23炭化水素からなる群から選択される、好ましくはC13、C17、C19、C21およびC23炭化水素からなる群から選択される少なくとも1つのさらなる直鎖状炭化水素を含有する。直鎖状飽和炭化水素が好ましい。好適な直鎖状C13炭化水素は、n−トリデカンである;好適な直鎖状C17炭化水素は、n−ヘプタデカンである;好適な直鎖状C19炭化水素は、n−ノナデカンである。
(a)50〜90重量%の直鎖状C−11炭化水素、好ましくはn−ウンデカン
(b)10〜50重量%の直鎖状C−15炭化水素、好ましくはn−ペンタデカン
を含有する、14C同位体含有炭化水素混合物に関する。
(a)55〜80重量%、特に60〜75重量%、特に65〜70重量%の直鎖状C11炭化水素、好ましくはn−ウンデカン
(b)20〜45重量%、特に24〜40重量%、特に24〜30重量%の直鎖状C15炭化水素、好ましくはn−ペンタデカン
を含有する、14C同位体含有炭化水素混合物が特に好ましい。
本発明の好ましい実施態様は、炭素数が1を超えて異なる少なくとも2つの異なる炭化水素を含有し、かつ直鎖状C13および直鎖状C15炭化水素を含有する、14C同位体含有炭化水素混合物に関する。直鎖状C13炭化水素は、好ましくはn−トリデカンである。直鎖状C15炭化水素は、好ましくはn−ペンタデカンである。本発明の好ましい実施態様において、本発明の炭化水素混合物は、直鎖状C13および直鎖状C15炭化水素、および、C11、C12、C14、C16、C17、C18、C19、C20、C21およびC23炭化水素からなる群から選択される、好ましくはC11、C17、C19、C21およびC23炭化水素からなる群から選択される少なくとも1つのさらなる直鎖状炭化水素を含有する。直鎖状飽和炭化水素が好ましい。好適な直鎖状C11炭化水素は、n−ウンデカンである;好適な直鎖状C17炭化水素は、n−ヘプタデカンである;好適な直鎖状C19炭化水素は、n−ノナデカンである。
(a)50〜90重量%の直鎖状C−13炭化水素、好ましくはn−トリデカン
(b)10〜50重量%の直鎖状C−15炭化水素、好ましくはn−ペンタデカン
を含有する、14C同位体含有炭化水素混合物に関する。
(a)55〜80重量%、特に60〜75重量%、特に65〜70重量%の直鎖状C13炭化水素、好ましくはn−トリデカン
(b)20〜45重量%、特に24〜40重量%、特に24〜30重量%の直鎖状C15炭化水素、好ましくはn−ペンタデカン
を含有する、14C同位体含有炭化水素混合物が特に好ましい。
本発明の好ましい実施態様において、直鎖状C15炭化水素に対する直鎖状C13炭化水素の重量比は、1.5〜3.5である。
本発明の好ましい実施態様は、炭素数が1を超えて異なる少なくとも2つの異なる炭化水素を含有し、かつ直鎖状C15および直鎖状C17炭化水素を含有する、14C同位体含有炭化水素混合物に関する。直鎖状C15炭化水素は、好ましくはn−ペンタデカンである。直鎖状C17炭化水素は、好ましくはn−ヘプタデカンである。本発明の好ましい実施態様において、本発明の炭化水素混合物は、直鎖状C15および直鎖状C17炭化水素、および、C11、C12、C13、C14、C16、C18、C19、C20、C21およびC23炭化水素からなる群から選択される、好ましくはC11、C13、C19、C21およびC23炭化水素からなる群から選択される少なくとも1つのさらなる直鎖状炭化水素を含有する。直鎖状飽和炭化水素が好ましい。好適な直鎖状C11炭化水素は、n−ウンデカンである;好適な直鎖状C13炭化水素は、n−トリデカンである;好適な直鎖状C19炭化水素は、n−ノナデカンである。
(a)50〜90重量%の直鎖状C15炭化水素、好ましくはn−ペンタデカン
(b)10〜50重量%の直鎖状C17炭化水素、好ましくはn−ヘプタデカン
を含有する、14C同位体含有炭化水素混合物に関する。
(a)55〜80重量%、特に60〜75重量%、特に65〜70重量%の直鎖状C15炭化水素、好ましくはn−ペンタデカン
(b)20〜45重量%、特に24〜40重量%、特に24〜30重量%の直鎖状C17炭化水素、好ましくはn−ヘプタデカン
を含有する、14C同位体含有炭化水素混合物が特に好ましい。
本発明の好ましい実施態様において、直鎖状C17炭化水素に対する直鎖状C15炭化水素の重量比は、1.5〜3.5である。
本発明の好ましい実施態様は、炭素数が1を超えて異なる少なくとも2つの異なる炭化水素を含有し、かつ直鎖状C17および直鎖状C19炭化水素を含有する、14C同位体含有炭化水素混合物に関する。直鎖状C17炭化水素は、好ましくはn−ヘプタデカンである。直鎖状C19炭化水素は、好ましくはn−ノナデカンである。本発明の好ましい実施態様において、本発明の炭化水素混合物は、直鎖状C17および直鎖状C19炭化水素、および、C11、C12、C13、C14、C15、C16、C18、C20、C21およびC23炭化水素からなる群から選択される、好ましくはC11、C13、C15、C21およびC23炭化水素からなる群から選択される少なくとも1つのさらなる直鎖状炭化水素を含有する。直鎖状飽和炭化水素が好ましい。好適な直鎖状C11炭化水素は、n−ウンデカンである;好適な直鎖状C13炭化水素は、n−トリデカンである;好適な直鎖状C15炭化水素は、n−ペンタデカンである。特に好ましいさらなる直鎖状炭化水素は、n−ヘネイコサン(C21直鎖状、飽和)である。
(a)50〜90重量%の直鎖状C17炭化水素、好ましくはn−ヘプタデカン
(b)10〜50重量%の直鎖状C19炭化水素、好ましくはn−ノナデカン
を含有する、14C同位体含有炭化水素混合物に関する。
(a)55〜80重量%、特に60〜75重量%、特に65〜70重量%の直鎖状C17炭化水素、好ましくはn−ヘプタデカン
(b)20〜45重量%、特に24〜40重量%、特に24〜30重量%の直鎖状C19炭化水素、好ましくはn−ノナデカン
を含有する、14C同位体含有炭化水素混合物が特に好ましい。
本発明の好ましい実施態様において、直鎖状C19炭化水素に対する直鎖状C17炭化水素の重量比は、1.5〜3.5である。
本発明の好ましい実施態様は、炭素数が1を超えて異なる少なくとも2つの異なる炭化水素を含有し、かつ直鎖状C19および直鎖状C21炭化水素を含有する、14C同位体含有炭化水素混合物に関する。直鎖状C19炭化水素は、好ましくはn−ノナデカンである。直鎖状C21炭化水素は、好ましくはn−ヘネイコサンである。本発明の好ましい実施態様において、本発明の炭化水素混合物は、直鎖状C19および直鎖状C21炭化水素、および、C11、C12、C13、C14、C15、C16、C17、C18、C20およびC23炭化水素からなる群から選択される、好ましくはC11、C13、C15、C17およびC23炭化水素からなる群から選択される少なくとも1つのさらなる直鎖状炭化水素を含有する。直鎖状飽和炭化水素が好ましい。好適な直鎖状C11炭化水素は、n−ウンデカンである;好適な直鎖状C13炭化水素は、n−トリデカンである;好適な直鎖状C17炭化水素は、n−ヘプタデカンである。
(a)50〜90重量%の直鎖状C19炭化水素、好ましくはn−ノナデカン
(b)10〜50重量%の直鎖状C21炭化水素、好ましくはn−ヘネイコサン
を含有する、14C同位体含有炭化水素混合物に関する。
(a)55〜80重量%、特に60〜75重量%、特に65〜70重量%の直鎖状C19炭化水素、好ましくはn−ノナデカン
(b)20〜45重量%、特に24〜40重量%、特に24〜30重量%の直鎖状C21炭化水素、好ましくはn−ヘネイコサン
を含有する、14C同位体含有炭化水素混合物が特に好ましい。
本発明の好ましい実施態様において、直鎖状C21炭化水素に対する直鎖状C19炭化水素の重量比は、1.5〜3.5である。
本発明の炭化水素混合物は、特に皮膚および/または毛髪ケア用の化粧品製剤における使用に適している。
本発明の炭化水素混合物は、特に日焼け防止用の化粧品製剤における使用に適している。
本発明の炭化水素混合物は、例えば、植物性脂肪アルコールの還元的脱メチル化により得ることができる。本発明の炭化水素混合物を製造するための特に適当な方法は、国際出願PCT/EP2006/011647(Cognis)に記載される、植物由来の脂肪アルコールからの還元的脱ヒドロキシメチル化の方法である。この方法において、例えば、所望の炭素鎖長の脂肪アルコールに対して上記方法中の個々の工程を施し、その結果得られる炭化水素を混合し、本発明の炭化水素混合物得ることができる。しかしながら、対応する脂肪アルコールを含有する混合物を直接還元的脱ヒドロキシメチル化することが好ましく、その結果直接的に得られる反応生成物は本発明の炭化水素混合物である。その後、これは、さらなる精製なしに、直接的に化粧品および/または医薬品製剤に使用することができる。
さらに、本発明は、0.1〜80重量%、好ましくは5〜50重量%、特に10〜30重量%の14C含有炭化水素混合物を含む化粧品および/または医薬品製剤に関する。重量%は、化粧品および/または医薬品製剤の総重量に基づく。
−直鎖状C11および直鎖状C13炭化水素、
−直鎖状C11および直鎖状C15炭化水素、
−直鎖状C13および直鎖状C15炭化水素、
−直鎖状C15および直鎖状C17炭化水素、
−直鎖状C17および直鎖状C19炭化水素および/または
−直鎖状C19および直鎖状C21炭化水素
からなる群から選択される炭化水素混合物を、0.1〜80重量%、好ましくは5〜50重量%、特に10〜30重量%含有する。
−炭素数nの炭化水素を50〜90重量%含有し、
−炭素数n+2の炭化水素を10〜50重量%含有する[nは7〜23の整数、好ましくは11〜21である]、
14C同位体含有炭化水素混合物を0.1〜80重量%含む化粧品および/または医薬品製剤が、特に好ましく挙げられる。
−炭素数nの炭化水素を55〜80重量%、特に60〜75重量%、特に65〜70重量%含有し、
−炭素数n+2の炭化水素を20〜45重量%、特に24〜40重量%、特に24〜30重量%含有する[nは7〜23の整数、好ましくは11〜21である]、
14C同位体含有炭化水素混合物を0.1〜80重量%含む化粧品および/または医薬品製剤が、特に好ましく挙げられる。
制汗剤は、アルミニウム、ジルコニウムまたは亜鉛の塩である。そのような適当なアンチハイドロティック(antihydrotic)活性成分は、例えばアルミニウムクロリド、アルミニウムクロロヒドレート、アルミニウムジクロロヒドレート、アルミニウムセスキクロロヒドレート、およびそれらと例えば1 ,2−プロピレングリコールとの錯体、アルミニウムヒドロキシアラントイネート、アルミニウムクロリドタートレート、アルミニウムジルコニウムトリクロロヒドレート、アルミニウムジルコニウムテトラクロロヒドレート、アルミニウムジルコニウムペンタクロロヒドレート、およびそれらと例えばグリシンのようなアミノ酸との錯体である。アルミニウムクロロヒドレート、アルミニウムジルコニウムテトラクロロヒドレート、アルミニウムジルコニウムペンタクロロヒドレートおよびそれらの錯体が好ましく挙げられる。
脇の下での発汗において、細菌は細胞外酵素(エステラーゼ、好ましくはプロテアーゼおよび/またはリパーゼ)を形成する。それらは汗に存在するエステルを開裂し、その結果臭気物質を放出する。適当なエステラーゼ阻害剤は、好ましくはクエン酸トリアルキル、例えばクエン酸トリメチル、クエン酸トリプロピル、クエン酸トリイソプロピル、クエン酸トリブチル、および特にクエン酸トリエチル(独国デュッセルドルフ、Cognis GmbH、Hydagen(登録商標)CAT)である。該物質は、酵素活性を阻害し、それにより臭気形成を減少させる。他のエステラーゼ阻害剤は、ステロールスルフェートまたはホスフェート、例えばラノステロール、コレステロール、カンペステロール、スチグマステロールおよびシトステロールスルフェートまたはホスフェート、ジカルボン酸およびそのエステル、例えばグルタル酸、グルタル酸モノエチルエステル、グルタル酸ジエチルエステル、アジピン酸、アジピン酸モノエチルエステル、アジピン酸ジエチルエステル、マロン酸およびマロン酸ジエチルエステル、ヒドロキシカルボン酸およびそのエステル、例えばクエン酸、リンゴ酸、酒石酸または酒石酸ジエチルエステル、および亜鉛グリシネートである。
適当な殺菌または静菌活性成分の典型例は、特にキトサンおよびフェノキシエタノールである。5−クロロ−2−(2,4−ジクロロフェノキシ)フェノールも特に効果的であることが見出されており、これはスイス、バーゼルのCiba-GeigyよりIrgasan(登録商標)の商標の下販売されている。適当な殺菌剤は、原則として、グラム陽性菌に対して作用する全ての物質、例えば、4−ヒドロキシ安息香酸およびその塩ならびにそのエステル、N−(4−クロロフェニル)−N’−(3,4−ジクロロフェニル)尿素、2,4,4’−トリクロロ−2’−ヒドロキシジフェニルエーテル(トリクロサン)、4−クロロ−3,5−ジメチルフェノール、2,2’−メチレンビス(6−ブロモ−4−クロロフェノール)、3−メチル−4−(1−メチルエチル)フェノール、2−ベンジル−4−クロロフェノール、3−(4−クロロフェニル)−1,2−プロパンジオール、3−ヨード−2−プロピニルブチルカルバメート、クロロヘキシジン、3,4,4’−トリクロロカーバニリド(TTC)、抗細菌香料、チモール、タイム油、オイゲノール、チョウジ油、メントール、ミント油、ファルネソール、フェノキシエタノール、グリセリルモノカプレート、グリセリルモノカプリレート、グリセリルモノラウレート(GML)、ジグリセリルモノカプレート(DMC)、N−アルキルサリチルアミド、例えば、n−オクチルサリチルアミドまたはn−デシルサリチルアミドである。
使用し得る汗吸着物質は、変成デンプン、例えばDry Flo Plus(National Starch)、ケイ酸塩、タルクおよび汗の吸着に適当であると思われる他の同様の多形物質である。本発明の製剤は、化粧品および/または医薬品製剤の総重量に基づいて、0.1〜30重量%、好ましくは1〜20重量%、特に2〜8重量%の量の汗吸着物質を含有し得る。
・EP0693471B1に記載されるような3−ベンジリデンカンファーまたは3−ベンジリデンノルカンファー(Mexoryl SDS 20)およびその誘導体、例えば、3−(4−メチルベンジリデン)カンファー;
・3−(4’−トリメチルアンモニウム)ベンジリデンボルナン−2−オンメチルスルフェート(Mexoryl SO);
・3,3’−(1,4−フェニレンジメチン)ビス(7,7−ジメチル−2−オキソビシクロ[2.2.1]ヘプタン−1−メタンスルホン酸)およびその塩(Mexoryl SX);
・3−(4’−スルホ)ベンジリデンボルナン−2−オンおよびその塩(Mexoryl SL);
・N−{(2および4)−[2−オキソボルン−3−イリデン)−メチル}ベンジル]アクリルアミド(Mexoryl SW)のポリマー;
・2−(2H−ベンゾトリアゾール−2−イル)−4−メチル−6−(2−メチル−3−(1,3,3,3−テトラメチル−1−(トリメチルシリルオキシ)−ジシロキサニル)プロピル)フェノール(Mexoryl SL);
・4−アミノ安息香酸誘導体、好ましくは2−エチルヘキシル4−(ジメチルアミノ)ベンゾエート、2−オクチル4−(ジメチルアミノ)ベンゾエートおよびアミル4−(ジメチル−アミノ)ベンゾエート;
・桂皮酸のエステル、好ましくは2−エチルヘキシル4−メトキシシンナメート、プロピル4−メトキシシンナメート、イソアミル4−メトキシシンナメート、2−エチルヘキシル2−シアノ−3,3−フェニルシンナメート(オクトクリレン);
・サリチル酸エステル、好ましくは2−エチルヘキシルサリチレート、4−イソプロピルベンジルサリチレート、ホモ−メンチルサリチレート;
・ベンゾフェノン誘導体、好ましくは2−ヒドロキシ−4−メトキシベンゾフェノン、2−ヒドロキシ−4−メトキシ−4’−メチルベンゾフェノン、2,2’−ジヒドロキシ−4−メトキシベンゾフェノン;
・ベンザルマロン酸のエステル、好ましくはジ−2−エチルヘキシル4−メトキシベンズマロネート;
・EP0818450A1に記載されるようなトリアジン誘導体、例えば、2,4,6−トリアニリノ(p−カルボ−2’−エチル−1’−ヘキシルオキシ)−1,3,5−トリアジンおよび2,4,6−トリス[p−(2−エチルヘキシルオキシ−カルボニル)アニリノ]−1,3,5−トリアジン(Uvinul T 150)、またはビス(2−エチルヘキシル)4,4’−[(6−[4−((1,1−ジメチルエチル)アミノカルボニル)−フェニルアミノ]−1,3,5−トリアジン−2,4−ジイル)ジイミノ]−ベンゾエート(Uvasorb(登録商標)HEB);
・2,2−(メチレンビス(6−(2H−ベンゾトリアゾール−2−イル)−4−(1,1,3,3−テトラメチルブチル)フェノール)(Tinosorb M);
・2,4−ビス[4−(2−エチルヘキシルオキシ)−2−ヒドロキシフェニル]−6−(4−メトキシフェニル)−1,3,5−トリアジン(Tinosorb S);
・プロパン−1,3−ジオン、例えば、1−(4−tert−ブチルフェニル)−3−(4’−メトキシフェニル)プロパン−1,3−ジオン;
・EP0694521B1に記載されるようなケトトリシクロ(5.2.1.0)デカン誘導体;
・ジメチコジエチルベンザルマロネート(Parsol SLX)。
・2−フェニルベンズイミダゾール−5−スルホン酸およびそのアルカリ金属塩、アルカリ土類金属塩、アンモニウム塩 アルキルアンモニウム塩、アルカノールアンモニウム塩およびグルカンモニウム塩;
・2,2−((1,4−フェニレン)ビス(1H−ベンズイミダゾール−4,6−ジスルホン酸、モノナトリウム塩)(Neo Heliopan AP);
・ベンゾフェノンのスルホン酸誘導体、好ましくは、2−ヒドロキシ−4−メトキシベンゾフェノン−5−スルホン酸およびその塩;
・3−ベンジリデンカンファーのスルホン酸誘導体例えば4−(2−オキソ−3−ボルニリデンメチル)−ベンゼンスルホン酸および2−メチル−5−(2−オキソ−3−ボルニリデン)−スルホン酸ならびにその塩。
NeoHeliopan(登録商標)MBC(INCI:4−メチルベンジリデンカンファー、Symrise製);NeoHeliopan(登録商標)BB(INCI:ベンゾフェノン−3、Symrise製);Parsol(登録商標)1789(INCI:ブチルメトキシジベンゾイルメタン、Hoffmann-La Roche (Givaudan)製);Tinosorb(登録商標)S(INCI:ビス−エチルヘキシルオキシフェノールメトキシフェニルトリアジン);Tinosorb(登録商標)M(INCI:メチレンビス−ベンゾトリアゾリルテトラメチルブチルフェノール、Ciba Specialty Chemicals Corporation製);Uvasorb(登録商標)HEB(INCI:ジエチルヘキシルブタミドトリアゾン、3V Inc.製);Uvinul(登録商標)T150(INCI:エチルヘキシルトリアゾン、BASF AG製);Uvinul(登録商標)A plus(INCI:ジエチルアミノヒドロキシベンゾイルヘキシルベンゾエート、BASF AG製);Mexoryl(登録商標)SO:3−(4’−トリメチルアンモニウム)ベンジリデンボルナン−2−オンメチルスルフェート、INCI:カンファーベンザルコニウムメトスルフェート;Mexoryl(登録商標)SX:3,3’−(1,4−フェニレンジメチン)ビス(7,7−ジメチル−2−オキソビシクロ[2.2.1]ヘプタン−1−メタンスルホン酸)、CTFA:INCIテレフタルイリデンジカンファースルホン酸;Mexoryl(登録商標)SL:3−(4’−スルホ)ベンジリデンボルナン−2−オン、INCIベンジリデンカンファースルホン酸;Mexoryl(登録商標)SW:N−{(2および4)−[2−オキソボルン−3−イリデン)メチル}ベンジル]アクリルアミドのポリマー、INCIポリアクリルアミドメチルベンジリデンカンファー;Mexoryl(登録商標)SL:2−(2H−ベンゾトリアゾール−2−イル)−4−メチル−6−(2−メチル−3−(1,3,3,3−テトラメチル−1−(トリメチルシリルオキシ)ジシロキサニル)プロピル)フェノール;INCI:ドロメトリゾールトリシロキサン;Parsol(登録商標)SLX:ジメチコジエチルベンズマロネート、INCIポリシリコン−15。
本発明の組成物は、一般的に、化粧品および/または医薬品製剤の総重量に基づいて、1〜10重量%、特に2〜5重量%の濃度のセルフタンニング剤を含有する。
したがって、本発明は、0.1〜80重量%の14C同位体含有炭化水素混合物と、少なくとも1つの顔料および/または染料を含有する化粧品および/または医薬品製剤を提供する。
該顔料は、個々にまたは混合物のいずれで存在していてもよい。
染料は、合成由来または天然由来のいずれであってもよい。適当な染料のリストをEP1371359A2の第8頁、第25〜27行、第9頁および第10頁ならびに第11頁、第1〜54行において見出すことができ、これをここで明らかに参照する。
本発明の薬剤は、一般的には、化粧品および/または医薬品製剤の総重量に基づいて、0.01〜5重量%、好ましくは0.1〜1.0重量%の染料を含有する。本発明の製剤は、一般的には、化粧品および/または医薬品製剤の総重量に基づいて、0.01〜30重量%の範囲の、特に0.1〜15重量%の範囲の、好ましくは1〜10重量%の範囲の総量の染料および顔料を含有する。
本発明の1つの実施態様において、本発明の製剤は、少なくとも1つの乳化剤を含有する。
したがって、本発明は、0.1〜80重量%の14C同位体含有炭化水素混合物と、少なくとも1つの乳化剤を含有する化粧品および/または医薬品製剤を提供する。
HLB値は、乳化剤の親水性基および親油性基の大きさや強さの平衡のようなものをいう。
本発明の1つの実施態様において、本発明の製剤は1つより多くの乳化剤を含有する。他の成分により、当業者は従来の乳化系(例えば、乳化剤および共乳化剤)を使用する。
非イオン性乳化剤の群には、例えば以下のものが含まれる:
(1)8〜40個の炭素原子を含有する直鎖状脂肪アルコール、12〜40個の炭素原子を含有する脂肪酸およびアルキル基中に8〜15個の炭素原子を含有するアルキルフェノールへの、2〜50モルのエチレンオキシドおよび/または1〜20モルのプロピレンオキシドの付加生成物;
(2)グリセロールへの1〜50モルのエチレンオキシド付加生成物のC12−18脂肪酸モノエステルおよびジエステル;
(3)6〜22個の炭素原子を含有する飽和および不飽和脂肪酸のソルビタンモノエステルおよびジエステル、ならびにそのエチレンオキシド付加生成物;
(4)アルキル基中に8〜22個の炭素原子を含有するアルキルモノおよびオリゴグリコシドおよびそのエトキシル化類似体;
(5)ヒマシ油および/または水添ヒマシ油への7〜60モルのエチレンオキシドの付加生成物;
(6)ポリオールエステル、および、特にポリグリセリルエステル、例えばポリオールポリ−12−ヒドロキシステアレート、ポリグリセリルポリリシノレエート、ポリグリセリルジイソステアレートまたはポリグリセリルダイメレートなど。これらのクラスの幾つかの化合物の混合物も同様に適当である;
(7)ヒマシ油および/または水添ヒマシ油への2〜15モルのエチレンオキシドの付加生成物;
(8)直鎖状、分枝状、不飽和または飽和C6−22脂肪酸、リシノール酸および12−ヒドロキシステアリン酸と、ポリグリセロール、ペンタエリスリトール、ジペンタエリスリトール、糖アルコール(例えばソルビトール)、アルキルグルコシド(例えばメチルグルコシド、ブチルグルコシド、ラウリルグルコシド)およびポリグルコシド(例えばセルロース)に基づく部分エステル、または混合エステル、例えばグリセリルステアレートシトレートおよびグリセリルステアレートラクテート;
(9)ポリシロキサン−ポリアルキル−ポリエーテル共重合体または対応する誘導体;
(10)ペンタエリスリトール、脂肪酸、クエン酸および脂肪アルコールの混合エステルおよび/または6〜22個の炭素原子を含有する脂肪酸、メチルグルコースおよびポリオール、好ましくはグリセロールまたはポリグリセロールの混合エステル。
本発明中、特に有利に使用し得る界面活性物質のさらなる例は、セチルPEG/PPG−10/1ジメチコン(セチルジメチコンコポリオール)であり、それらは、Evonik GoldschmidtからABIL(登録商標)EM 90の商品名のもと市販されている。
本発明中、特に有利に使用し得る界面活性物質のさらなる例は、シクロメチコンジメチコンコポリオールであり、それらは、Evonik GoldschmidtからABIL(登録商標)EM 97およびABIL(登録商標)WE 09の商品名のもと市販されている。
さらに、乳化剤ラウリルPEG/PPG−18/18メチコン(ラウリルメチコンコポリオール)が非常に有利であることが見出されている。それは、Dow Corning(登録商標)5200 Formulation Aidの商品名のもとDow Corning Ltdから市販されている。
さらに有利なシリコーン乳化剤は、Wackerからのオクチルジメチコンエトキシグルコシドである。本発明のシリコーン油中水型エマルションに対して、このタイプのエマルションに使用される全ての既知の乳化剤を使用し得る。本発明に特に好ましいシリコーン中水型乳化剤は、セチルPEG/PPG−10/1ジメチコンおよびラウリルPEG/PPG−18/18メチコン(例えば、ABIL(登録商標)EM 90(Evonik Goldschmidt)、DC5200 Formulation Aid(Dow Corning))およびこの2つの乳化剤の所望の全混合物である。
本発明の1つの実施態様において、本発明の製剤は少なくとも1つの界面活性剤を含有する。
界面活性剤は、一般的に、20より大きなHLB値を有する界面活性物質を意味すると理解される。
本発明の1つの実施態様において、本発明の製剤は少なくとも1つのワックス成分を含有する。
本発明の1つの実施態様において、本発明の製剤は少なくとも1つのポリマーを含有する。
本発明は、0.1〜80重量%の14C同位体含有炭化水素混合物と、少なくとも1つのポリマーを含有する化粧品および/または医薬品製剤を提供する。
本発明の実施態様において、本発明の製剤は少なくとも1つの油体を含有する。一般的に、本発明の製剤は、炭化水素混合物を油体として含有する。したがって、ここで、特定の好ましい実施態様において、本発明の製剤は、「さらなる油体」とも称される本発明の炭化水素混合物以外の油体を含有する。
本発明は、好ましくは、14C同位体を含有し、かつ炭化水素が、炭素数が1を超えて異なる、好ましくは2異なる少なくとも2つの異なる炭化水素を含有する炭化水素混合物0.1〜80重量%と、少なくとも1つの(さらなる)油体を含む化粧品および/または医薬品製剤を提供する。
本発明は、好ましくは、14C同位体を含有し、かつ炭化水素が、炭素数が1を超えて異なる、好ましくは2異なる少なくとも2つの異なる炭化水素を含有する炭化水素混合物0.1〜80重量%と、少なくとも1つの生体活性物質、防虫剤、チロシナーゼ阻害剤、防腐剤、香油、安定剤および/またはヒドロトロープを含む化粧品および/または医薬品製剤を提供する。
本発明の炭化水素混合物を調製するため、はじめに、互いに別々に、トリデカンおよびウンデカンを特定の脂肪アルコールから調製し、その後互いに対して所望の割合で混合した。
はじめに1000gの1−テトラデカノール(4.7モル;CognisからのLorol(登録商標)C14)を、10gのニッケル触媒(EngelhardからのNi-5249P;Ni含有量=63重量%)とともに攪拌圧力容器へ投入し、240℃まで加熱した。続いて、20barの圧力下、12時間にわたり散布チューブを介して水素を加え、同時に、反応ガスを容器の蓋にあるバルブを介して放出した。その後、生成物を冷却し、放出し、濾過した。最終重量845gの反応生成物が得られた。
はじめに1000gの1−ドデカノール(5.4モル;CognisからのLorol(登録商標)C12)を、10gのニッケル触媒(EngelhardからのNi-5249P;Ni含有量=63重量%)とともに攪拌圧力容器へ投入し、240℃まで加熱した。続いて、20barの圧力下、12時間にわたり散布チューブを介して水素を加え、同時に、反応ガスを容器の蓋にあるバルブを介して放出した。その後、生成物を冷却し、放出し、濾過した。最終重量835gの反応生成物が得られた。
実施例1の炭化水素混合物の組成物:76重量%のn−ウンデカン、24重量%のn−トリデカン。
本発明の炭化水素混合物を調製するため、調製される炭化水素混合物に対応するC12およびC14脂肪アルコールを含有する脂肪アルコール混合物を、還元的脱ヒドロキシメチル化した。
調製実施例2により得られる炭化水素混合物は、下記の組成を有する(GC分析)。
本発明の炭化水素混合物を調製するため、調製される炭化水素混合物に対応するC12、C14、C16およびC18脂肪アルコールを含有する脂肪アルコール混合物を、還元的脱ヒドロキシメチル化した:はじめに、1000gのLorol(登録商標)Technisch(Cognis;C12、C14、C16およびC18脂肪アルコールの脂肪アルコール混合物)および10gのニッケル触媒(EngelhardからのNi-5249P;Ni含有量=63重量%)をオートクレーブに投入した。該反応器を閉じ、真空にした。その後、反応混合物を、減圧下で攪拌しながら30分間、約80℃まで加熱した。その後、反応器を水素により約80barの状態にし、続けて250℃まで加熱した。圧力が一定のままで、大部分の脂肪アルコールが所望の炭化水素に変換された時、反応は完了する。窒素による減圧および放出後、生成物を蒸留により精製した。無色の液体として精製された生成物が得られた。
本発明の炭化水素混合物を調製するため、調製される炭化水素混合物に対応するC16およびC18脂肪アルコールを含有する脂肪アルコール混合物を、脱ヒドロキシメチル化した:はじめに、1000gのStenol(登録商標)16 65(Cognis;C16およびC18脂肪アルコールの脂肪アルコール混合物)および10gのニッケル触媒(EngelhardからのNi-5249P;Ni含有量=63重量%)をオートクレーブに投入した。該反応器を閉じ、真空にした。その後、反応混合物を、減圧下で攪拌しながら30分間、約80℃まで加熱した。その後、反応器を水素により約80barの状態にし、続けて250℃まで加熱した。圧力が一定のままで、大部分の脂肪アルコールが所望の炭化水素に変換された時、反応は完了する。窒素による減圧および放出後、生成物を蒸留により精製した。無色の液体として精製された生成物が得られた。
調製実施例4Cにより得られる炭化水素混合物は、以下の組成を有する(GC分析):C15炭化水素 30%、C17炭化水素 70%。
本発明の炭化水素混合物を調製するため、調製される炭化水素混合物に対応するC18、C20およびC22脂肪アルコールを含有する脂肪アルコール混合物を、脱ヒドロキシメチル化した:はじめに、1000gのStenol(登録商標)1822-45(Cognis;C18、C20およびC22脂肪アルコールの脂肪アルコール混合物)および10gのニッケル触媒(EngelhardからのNi-5249P;Ni含有量=63重量%)をオートクレーブに投入した。該反応器を閉じ、真空にした。その後、反応混合物を、減圧下で攪拌しながら30分間、約80℃まで加熱した。その後、反応器を水素により約80barの状態にし、続けて250℃まで加熱した。圧力が一定のままで、大部分の脂肪アルコールが所望の炭化水素に変換された時、反応は完了する。窒素による減圧および放出後、生成物を蒸留により精製した。無色の液体として精製された生成物が得られた。
調製実施例5Cにより得られる炭化水素混合物は、以下の組成を有する(GC分析):C17炭化水素 10%、C19炭化水素 15%、C21炭化水素 75%。
調製実施例2により得られたn−ウンデカンおよびn−トリデカンを、下記の脱臭スティック製剤に使用し、得られた製剤の硬度を試験した(全て重量%で表す)。
下記の処方にしたがって作製されたクリームは、5人の感覚的に熟練した被験者の一団により試験され、感覚的に「軽い」として評価された。
Claims (11)
- 14 C同位体を含有する炭化水素混合物であって、該炭化水素混合物に存在する炭化水素の総量に基づいて、
(a)55〜80重量%の直鎖状C11炭化水素、および
(b)20〜45重量%の直鎖状C13炭化水素または直鎖状C15炭化水素
を含有し、炭化水素の総量に基づいて0〜5重量%の分枝状炭化水素を含有する、化粧品において使用される炭化水素混合物。 - 炭化水素混合物が、炭化水素混合物に存在する炭化水素の総量に基づいて、1重量%以下の分枝状炭化水素を含有する、請求項1に記載の炭化水素混合物。
- (a)直鎖状C11炭化水素および(b)直鎖状C13炭化水素または直鎖状C15炭化水素が、炭化水素混合物に存在する炭化水素の総量に基づいて、少なくとも80重量%を構成する、請求項1または2に記載の炭化水素混合物。
- さらに、直鎖状C17、C19、C21およびC23炭化水素およびそれらの混合物からなる群から選択される少なくとも1つの直鎖状炭化水素を含む、請求項1〜3のいずれかに記載の炭化水素混合物。
- (b)の炭化水素が直鎖状C15炭化水素であり、さらに直鎖状C17炭化水素を含有する、請求項1〜4のいずれかに記載の炭化水素混合物。
- さらに、直鎖状C17および直鎖状C19炭化水素を含有する、請求項1〜5のいずれかに記載の炭化水素混合物。
- さらに少なくとも1つの直鎖状C21炭化水素を含有する、請求項6に記載の炭化水素混合物。
- 化粧品における油体および/または分散剤としての、請求項1〜7のいずれかに記載の炭化水素混合物の使用。
- 0.1〜80重量%の請求項1〜7のいずれかに記載の14C同位体含有炭化水素混合物を含有する化粧品。
- 少なくとも1つの制汗/脱臭活性成分を含有する、請求項9に記載の化粧品。
- 少なくとも1つの乳化剤および/または界面活性剤および/またはワックス成分および/またはポリマーおよび/またはさらなる油体を含有する、請求項9または10に記載の化粧品。
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- 2008-06-12 CN CN200880020883.5A patent/CN101677920B/zh active Active
- 2008-06-12 WO PCT/EP2008/004702 patent/WO2008155060A2/de active Application Filing
- 2008-06-12 EP EP08759204A patent/EP2162114A2/de not_active Ceased
- 2008-06-12 KR KR1020097026545A patent/KR20100031508A/ko active Search and Examination
- 2008-06-12 US US12/665,532 patent/US20110059032A1/en not_active Abandoned
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Also Published As
Publication number | Publication date |
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US8956598B2 (en) | 2015-02-17 |
WO2008155060A2 (de) | 2008-12-24 |
US20170035665A1 (en) | 2017-02-09 |
US20110059032A1 (en) | 2011-03-10 |
JP5988542B2 (ja) | 2016-09-07 |
CN101677920B (zh) | 2015-06-03 |
US20100189673A1 (en) | 2010-07-29 |
CN101677923B (zh) | 2015-07-15 |
ZA200909059B (en) | 2011-05-25 |
JP2010530389A (ja) | 2010-09-09 |
KR20100031509A (ko) | 2010-03-22 |
JP2010531809A (ja) | 2010-09-30 |
WO2008155060A3 (de) | 2009-11-12 |
CN101677920A (zh) | 2010-03-24 |
KR101553415B1 (ko) | 2015-09-15 |
KR20100031508A (ko) | 2010-03-22 |
EP2167023A2 (de) | 2010-03-31 |
CN101677923A (zh) | 2010-03-24 |
US10537505B2 (en) | 2020-01-21 |
EP2162114A2 (de) | 2010-03-17 |
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