JP2008533070A5 - - Google Patents
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- Publication number
- JP2008533070A5 JP2008533070A5 JP2008501201A JP2008501201A JP2008533070A5 JP 2008533070 A5 JP2008533070 A5 JP 2008533070A5 JP 2008501201 A JP2008501201 A JP 2008501201A JP 2008501201 A JP2008501201 A JP 2008501201A JP 2008533070 A5 JP2008533070 A5 JP 2008533070A5
- Authority
- JP
- Japan
- Prior art keywords
- propylheptyl
- acid
- acid ester
- ester
- diester
- 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.)
- Granted
Links
- 239000000203 mixture Substances 0.000 claims description 52
- 150000002148 esters Chemical class 0.000 claims description 40
- YLQLIQIAXYRMDL-UHFFFAOYSA-N propylheptyl alcohol Chemical compound CCCCCC(CO)CCC YLQLIQIAXYRMDL-UHFFFAOYSA-N 0.000 claims description 18
- -1 2-propylheptyl-n-undecenoic acid ester Chemical class 0.000 claims description 14
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims description 13
- 229920006395 saturated elastomer Polymers 0.000 claims description 13
- BZAVPCPYQNOAKD-UHFFFAOYSA-N 2-(2-propylheptyl)decanoic acid Chemical compound CCCCCCCCC(C(O)=O)CC(CCC)CCCCC BZAVPCPYQNOAKD-UHFFFAOYSA-N 0.000 claims description 10
- YUIXJOTYLXMLCO-UHFFFAOYSA-N 2-(2-propylheptyl)dodecanoic acid Chemical compound C(CC)C(CC(C(=O)O)CCCCCCCCCC)CCCCC YUIXJOTYLXMLCO-UHFFFAOYSA-N 0.000 claims description 10
- MQDHEAVTLZSSFJ-UHFFFAOYSA-N 2-butyl-4-propylnonanoic acid Chemical compound CCCCCC(CCC)CC(C(O)=O)CCCC MQDHEAVTLZSSFJ-UHFFFAOYSA-N 0.000 claims description 10
- YHRCTDSVDHUXLM-UHFFFAOYSA-N 2-heptyl-4-propylnonanoic acid Chemical compound C(CC)C(CC(C(=O)O)CCCCCCC)CCCCC YHRCTDSVDHUXLM-UHFFFAOYSA-N 0.000 claims description 10
- WGTXQQXNSZKTJZ-UHFFFAOYSA-N 2-hexyl-4-propylnonanoic acid Chemical compound CCCCCCC(C(O)=O)CC(CCC)CCCCC WGTXQQXNSZKTJZ-UHFFFAOYSA-N 0.000 claims description 10
- FPHQIBVXUWIFSQ-UHFFFAOYSA-N C(CC)C(CC(C(=O)O)CC)CCCCC Chemical compound C(CC)C(CC(C(=O)O)CC)CCCCC FPHQIBVXUWIFSQ-UHFFFAOYSA-N 0.000 claims description 10
- NXDLHPXSRPQFBC-UHFFFAOYSA-N C(CC)C(CC(C(=O)O)CCC)CCCCC Chemical compound C(CC)C(CC(C(=O)O)CCC)CCCCC NXDLHPXSRPQFBC-UHFFFAOYSA-N 0.000 claims description 10
- AEFRJEYOHNJTQW-UHFFFAOYSA-N C(CC)C(CC(C(=O)O)CCCCC)CCCCC Chemical compound C(CC)C(CC(C(=O)O)CCCCC)CCCCC AEFRJEYOHNJTQW-UHFFFAOYSA-N 0.000 claims description 10
- OKSVPBAIEURUNK-UHFFFAOYSA-N 2-(2-propylheptyl)undecanoic acid Chemical compound C(CC)C(CC(C(=O)O)CCCCCCCCC)CCCCC OKSVPBAIEURUNK-UHFFFAOYSA-N 0.000 claims description 8
- 239000002253 acid Substances 0.000 claims description 7
- 239000002537 cosmetic Substances 0.000 claims description 6
- 239000003995 emulsifying agent Substances 0.000 claims description 4
- 229920000642 polymer Polymers 0.000 claims description 4
- 239000004094 surface-active agent Substances 0.000 claims description 4
- 239000003814 drug Substances 0.000 claims description 3
- 238000004519 manufacturing process Methods 0.000 claims description 3
- 239000003054 catalyst Substances 0.000 claims description 2
- 150000004702 methyl esters Chemical class 0.000 claims description 2
- 239000008194 pharmaceutical composition Substances 0.000 claims description 2
- 238000005809 transesterification reaction Methods 0.000 claims description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 2
- 150000001735 carboxylic acids Chemical class 0.000 claims 6
- 150000005690 diesters Chemical class 0.000 claims 3
- 229920000305 Nylon 6,10 Polymers 0.000 claims 2
- 229960000250 adipic acid Drugs 0.000 claims 2
- 229960005137 succinic acid Drugs 0.000 claims 2
- UKQUXDRVODMRIU-UHFFFAOYSA-N 2-propylheptyl 2-methylprop-2-enoate Chemical compound CCCCCC(CCC)COC(=O)C(C)=C UKQUXDRVODMRIU-UHFFFAOYSA-N 0.000 claims 1
- 229960002255 azelaic acid Drugs 0.000 claims 1
- 150000001991 dicarboxylic acids Chemical class 0.000 claims 1
- TVIDDXQYHWJXFK-UHFFFAOYSA-N n-Dodecanedioic acid Natural products OC(=O)CCCCCCCCCCC(O)=O TVIDDXQYHWJXFK-UHFFFAOYSA-N 0.000 claims 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 12
- KUTCZKWCZNAIJY-UHFFFAOYSA-N 2,2-dipropyloctanoic acid Chemical class CCCCCCC(CCC)(CCC)C(O)=O KUTCZKWCZNAIJY-UHFFFAOYSA-N 0.000 description 2
- SGHGTXZNRUKTRY-UHFFFAOYSA-N 2-(3-methyl-2-propylhexyl)decanoic acid Chemical compound CC(C(CC(C(=O)O)CCCCCCCC)CCC)CCC SGHGTXZNRUKTRY-UHFFFAOYSA-N 0.000 description 2
- NUKHBNPSGNZGRS-UHFFFAOYSA-N 2-(3-methyl-2-propylhexyl)dodecanoic acid Chemical compound CC(C(CC(C(=O)O)CCCCCCCCCC)CCC)CCC NUKHBNPSGNZGRS-UHFFFAOYSA-N 0.000 description 2
- LXOLWYDVPYQSIW-UHFFFAOYSA-N 2-(3-methyl-2-propylhexyl)nonanoic acid Chemical compound CC(C(CC(C(=O)O)CCCCCCC)CCC)CCC LXOLWYDVPYQSIW-UHFFFAOYSA-N 0.000 description 2
- BMZDGKNAVMLKGX-UHFFFAOYSA-N 2-(3-methyl-2-propylhexyl)undecanoic acid Chemical compound CC(C(CC(C(=O)O)CCCCCCCCC)CCC)CCC BMZDGKNAVMLKGX-UHFFFAOYSA-N 0.000 description 2
- JRHAAXBDKJDOLD-UHFFFAOYSA-N 2-(4-methyl-2-propylhexyl)decanoic acid Chemical compound CCCCCCCCC(C(O)=O)CC(CCC)CC(C)CC JRHAAXBDKJDOLD-UHFFFAOYSA-N 0.000 description 2
- AABSAALSNBGYBA-UHFFFAOYSA-N 2-(4-methyl-2-propylhexyl)dodecanoic acid Chemical compound CC(CC(CC(C(=O)O)CCCCCCCCCC)CCC)CC AABSAALSNBGYBA-UHFFFAOYSA-N 0.000 description 2
- MSMXMOHNSGJXMO-UHFFFAOYSA-N 2-(4-methyl-2-propylhexyl)nonanoic acid Chemical compound CC(CC(CC(C(=O)O)CCCCCCC)CCC)CC MSMXMOHNSGJXMO-UHFFFAOYSA-N 0.000 description 2
- JWVMODNSXOGNKX-UHFFFAOYSA-N 2-(4-methyl-2-propylhexyl)undecanoic acid Chemical compound CC(CC(CC(C(=O)O)CCCCCCCCC)CCC)CC JWVMODNSXOGNKX-UHFFFAOYSA-N 0.000 description 2
- RMSFNDLOCVZCDG-UHFFFAOYSA-N 2-butyl-5-methyl-4-propyloctanoic acid Chemical compound CC(C(CC(C(=O)O)CCCC)CCC)CCC RMSFNDLOCVZCDG-UHFFFAOYSA-N 0.000 description 2
- JZULUENMHCSUCC-UHFFFAOYSA-N 2-butyl-6-methyl-4-propyloctanoic acid Chemical compound CCCCC(C(O)=O)CC(CCC)CC(C)CC JZULUENMHCSUCC-UHFFFAOYSA-N 0.000 description 2
- SLSQUQLCCSEBQI-UHFFFAOYSA-N 2-ethyl-2-propyloctanoic acid Chemical class CCCCCCC(CC)(C(O)=O)CCC SLSQUQLCCSEBQI-UHFFFAOYSA-N 0.000 description 2
- WTHOQPDOXNGXGD-UHFFFAOYSA-N 2-ethyl-5-methyl-4-propyloctanoic acid Chemical compound CC(C(CC(C(=O)O)CC)CCC)CCC WTHOQPDOXNGXGD-UHFFFAOYSA-N 0.000 description 2
- VNSSWNSKIUDPRC-UHFFFAOYSA-N 2-ethyl-6-methyl-4-propyloctanoic acid Chemical compound CC(CC(CC(C(=O)O)CC)CCC)CC VNSSWNSKIUDPRC-UHFFFAOYSA-N 0.000 description 2
- IFBITJWLPGKPFA-UHFFFAOYSA-N 2-hexyl-2-propyldecanoic acid Chemical compound C(CC)C(C(O)=O)(CCCCCCCC)CCCCCC IFBITJWLPGKPFA-UHFFFAOYSA-N 0.000 description 2
- CACZSAHCLNHKDQ-UHFFFAOYSA-N 2-hexyl-2-propyldodecanoic acid Chemical compound C(CC)C(C(=O)O)(CCCCCCCCCC)CCCCCC CACZSAHCLNHKDQ-UHFFFAOYSA-N 0.000 description 2
- XEDHSHJVRLWASH-UHFFFAOYSA-N 2-hexyl-2-propylnonanoic acid Chemical class CCCCCCCC(CCC)(C(O)=O)CCCCCC XEDHSHJVRLWASH-UHFFFAOYSA-N 0.000 description 2
- LYBUSXFGLHZFPG-UHFFFAOYSA-N 2-hexyl-2-propyloctanoic acid Chemical class C(CC)C(C(=O)O)(CCCCCC)CCCCCC LYBUSXFGLHZFPG-UHFFFAOYSA-N 0.000 description 2
- VLUQNDDLNRMULH-UHFFFAOYSA-N 2-hexyl-5-methyl-4-propyloctanoic acid Chemical compound CC(C(CC(C(=O)O)CCCCCC)CCC)CCC VLUQNDDLNRMULH-UHFFFAOYSA-N 0.000 description 2
- WLAXTDFOELESRS-UHFFFAOYSA-N 2-hexyl-6-methyl-4-propyloctanoic acid Chemical compound CCCCCCC(C(O)=O)CC(CCC)CC(C)CC WLAXTDFOELESRS-UHFFFAOYSA-N 0.000 description 2
- JJUKNQOEMDFRTD-UHFFFAOYSA-N 2-pentyl-2-propyloctanoic acid Chemical class C(CCCCC)C(C(=O)O)(CCCCC)CCC JJUKNQOEMDFRTD-UHFFFAOYSA-N 0.000 description 2
- AJVGRRDXNHVISC-UHFFFAOYSA-N 5-methyl-2,4-dipropyloctanoic acid Chemical compound CC(C(CC(C(=O)O)CCC)CCC)CCC AJVGRRDXNHVISC-UHFFFAOYSA-N 0.000 description 2
- ZXYTVBBONYYLIE-UHFFFAOYSA-N 5-methyl-2-pentyl-4-propyloctanoic acid Chemical compound CC(C(CC(C(=O)O)CCCCC)CCC)CCC ZXYTVBBONYYLIE-UHFFFAOYSA-N 0.000 description 2
- MJDHNOZZQKCNKK-UHFFFAOYSA-N 6-methyl-2,4-dipropyloctanoic acid Chemical compound CC(CC(CC(C(=O)O)CCC)CCC)CC MJDHNOZZQKCNKK-UHFFFAOYSA-N 0.000 description 2
- JLOSMUURGISDLF-UHFFFAOYSA-N 6-methyl-2-pentyl-4-propyloctanoic acid Chemical compound CC(CC(CC(C(=O)O)CCCCC)CCC)CC JLOSMUURGISDLF-UHFFFAOYSA-N 0.000 description 2
- FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Chemical compound CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 description 2
- LXVPEMSKXJBXGR-UHFFFAOYSA-N CCCCCCC(CCC)(CCCC)C(O)=O Chemical class CCCCCCC(CCC)(CCCC)C(O)=O LXVPEMSKXJBXGR-UHFFFAOYSA-N 0.000 description 2
- YLKNSPKZDMZYSE-UHFFFAOYSA-N CCCCCCCCCC(CCC)(CCCCCC)C(O)=O Chemical class CCCCCCCCCC(CCC)(CCCCCC)C(O)=O YLKNSPKZDMZYSE-UHFFFAOYSA-N 0.000 description 2
- GWYFCOCPABKNJV-UHFFFAOYSA-N beta-methyl-butyric acid Natural products CC(C)CC(O)=O GWYFCOCPABKNJV-UHFFFAOYSA-N 0.000 description 2
- GHVNFZFCNZKVNT-UHFFFAOYSA-N decanoic acid Chemical compound CCCCCCCCCC(O)=O GHVNFZFCNZKVNT-UHFFFAOYSA-N 0.000 description 2
- MHPUGCYGQWGLJL-UHFFFAOYSA-N dimethyl pentanoic acid Natural products CC(C)CCCC(O)=O MHPUGCYGQWGLJL-UHFFFAOYSA-N 0.000 description 2
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 2
- MNWFXJYAOYHMED-UHFFFAOYSA-N heptanoic acid Chemical compound CCCCCCC(O)=O MNWFXJYAOYHMED-UHFFFAOYSA-N 0.000 description 2
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- YRHYCMZPEVDGFQ-UHFFFAOYSA-N n-decanoic acid methyl ester Natural products CCCCCCCCCC(=O)OC YRHYCMZPEVDGFQ-UHFFFAOYSA-N 0.000 description 2
- HNBDRPTVWVGKBR-UHFFFAOYSA-N n-pentanoic acid methyl ester Natural products CCCCC(=O)OC HNBDRPTVWVGKBR-UHFFFAOYSA-N 0.000 description 2
- FBUKVWPVBMHYJY-UHFFFAOYSA-N nonanoic acid Chemical compound CCCCCCCCC(O)=O FBUKVWPVBMHYJY-UHFFFAOYSA-N 0.000 description 2
- WWZKQHOCKIZLMA-UHFFFAOYSA-N octanoic acid Chemical compound CCCCCCCC(O)=O WWZKQHOCKIZLMA-UHFFFAOYSA-N 0.000 description 2
- ZDPHROOEEOARMN-UHFFFAOYSA-N undecanoic acid Chemical compound CCCCCCCCCCC(O)=O ZDPHROOEEOARMN-UHFFFAOYSA-N 0.000 description 2
- NQPDZGIKBAWPEJ-UHFFFAOYSA-N valeric acid Chemical compound CCCCC(O)=O NQPDZGIKBAWPEJ-UHFFFAOYSA-N 0.000 description 2
- SDNSCHDITWSFQA-UHFFFAOYSA-N 2-hexyl-3-propylundec-2-enoic acid Chemical class CCCCCCCCC(=C(CCCCCC)C(=O)O)CCC SDNSCHDITWSFQA-UHFFFAOYSA-N 0.000 description 1
- IGBBVTAVILYDIO-UHFFFAOYSA-N 2-undecenoic acid Chemical compound CCCCCCCCC=CC(O)=O IGBBVTAVILYDIO-UHFFFAOYSA-N 0.000 description 1
- UUIQMZJEGPQKFD-UHFFFAOYSA-N Methyl butyrate Chemical compound CCCC(=O)OC UUIQMZJEGPQKFD-UHFFFAOYSA-N 0.000 description 1
- XNCNNDVCAUWAIT-UHFFFAOYSA-N Methyl heptanoate Chemical compound CCCCCCC(=O)OC XNCNNDVCAUWAIT-UHFFFAOYSA-N 0.000 description 1
- 239000004480 active ingredient Substances 0.000 description 1
- 230000001166 anti-perspirative effect Effects 0.000 description 1
- 239000003213 antiperspirant Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 230000001815 facial effect Effects 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 239000000077 insect repellent Substances 0.000 description 1
- NUKZAGXMHTUAFE-UHFFFAOYSA-N methyl hexanoate Chemical compound CCCCCC(=O)OC NUKZAGXMHTUAFE-UHFFFAOYSA-N 0.000 description 1
- UQDUPQYQJKYHQI-UHFFFAOYSA-N methyl laurate Chemical compound CCCCCCCCCCCC(=O)OC UQDUPQYQJKYHQI-UHFFFAOYSA-N 0.000 description 1
- IJXHLVMUNBOGRR-UHFFFAOYSA-N methyl nonanoate Chemical compound CCCCCCCCC(=O)OC IJXHLVMUNBOGRR-UHFFFAOYSA-N 0.000 description 1
- JGHZJRVDZXSNKQ-UHFFFAOYSA-N methyl octanoate Chemical compound CCCCCCCC(=O)OC JGHZJRVDZXSNKQ-UHFFFAOYSA-N 0.000 description 1
- FDNCPIRKQFHDBX-UHFFFAOYSA-N methyl undec-2-enoate Chemical compound CCCCCCCCC=CC(=O)OC FDNCPIRKQFHDBX-UHFFFAOYSA-N 0.000 description 1
- XPQPWPZFBULGKT-UHFFFAOYSA-N methyl undecanoate Chemical compound CCCCCCCCCCC(=O)OC XPQPWPZFBULGKT-UHFFFAOYSA-N 0.000 description 1
- 239000004745 nonwoven fabric Substances 0.000 description 1
- 239000011505 plaster Substances 0.000 description 1
- 230000009759 skin aging Effects 0.000 description 1
- 230000000475 sunscreen effect Effects 0.000 description 1
- 239000000516 sunscreening agent Substances 0.000 description 1
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE102005012300.7 | 2005-03-17 | ||
| DE200510012300 DE102005012300A1 (de) | 2005-03-17 | 2005-03-17 | Kosmetische Zusammensetzungen enthaltend Ester auf Basis von 2-Propylheptanol |
| EP05012510 | 2005-06-10 | ||
| EP05012510.3 | 2005-06-10 | ||
| PCT/EP2006/002148 WO2006097235A1 (de) | 2005-03-17 | 2006-03-09 | Kosmetische zusammensetzungen enthaltend ester auf basis von 2- propylheptanol |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2008533070A JP2008533070A (ja) | 2008-08-21 |
| JP2008533070A5 true JP2008533070A5 (enExample) | 2009-04-23 |
| JP5275020B2 JP5275020B2 (ja) | 2013-08-28 |
Family
ID=36282562
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2008501201A Active JP5275020B2 (ja) | 2005-03-17 | 2006-03-09 | ２−プロピルヘプタノールに基づくエステルを含有する化粧品組成物 |
Country Status (7)
| Country | Link |
|---|---|
| US (3) | US8642652B2 (enExample) |
| EP (1) | EP1858480B3 (enExample) |
| JP (1) | JP5275020B2 (enExample) |
| KR (1) | KR101330963B1 (enExample) |
| CN (1) | CN101141944B (enExample) |
| ES (1) | ES2424750T7 (enExample) |
| WO (1) | WO2006097235A1 (enExample) |
Families Citing this family (35)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP1905419A1 (de) * | 2006-09-20 | 2008-04-02 | Cognis IP Management GmbH | Kosmetische Zubereitung und Ölkörper Mischungen |
| JP5529538B2 (ja) * | 2006-09-29 | 2014-06-25 | ユニオン カーバイド ケミカルズ アンド プラスティックス テクノロジー エルエルシー | パーソナルケア製品用の４級化セルロースエーテル |
| DE102007017536B4 (de) | 2007-04-11 | 2025-06-26 | Cognis Ip Management Gmbh | Octanoat-haltige Emulsion |
| DE102007017439A1 (de) | 2007-04-11 | 2008-10-16 | Beiersdorf Ag | Octanoat-haltige Zubereitung mit Phenylen-1,4-bis-(2-benz-imi-dazyl)-3,3'-5,5'-tetrasulfonsäuresalzen |
| DE102007017435A1 (de) | 2007-04-11 | 2008-10-16 | Beiersdorf Ag | Octanoat-haltige Zubereitung mit Salicylaten |
| DE102007017434A1 (de) | 2007-04-11 | 2008-10-16 | Beiersdorf Ag | Emulsion mit Octanoat |
| DE102007017436A1 (de) | 2007-04-11 | 2008-10-16 | Beiersdorf Ag | Octanoat-haltige Zubereitung mit Triazinen |
| DE102007017440A1 (de) | 2007-04-11 | 2008-10-16 | Beiersdorf Ag | Octanoat-haltige Zubereitung mit 2-(4'-Diethylamino-2'-hydoxybenzoyl)-benzoesäurehexylester |
| DE102007017437A1 (de) | 2007-04-11 | 2008-10-16 | Beiersdorf Ag | Octanoat-haltige Pigmentzubereitung |
| DE102007017438A1 (de) | 2007-04-11 | 2008-10-16 | Beiersdorf Ag | Octanoat-haltige Zubereitung mit Dimethicondiethylbenzalmalonat |
| EP1985279A1 (de) * | 2007-04-26 | 2008-10-29 | Cognis IP Management GmbH | Kosmetische Zusammensetzungen enthaltend Ester auf Basis von 2-Propylheptanol |
| 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 |
| DE102008052521A1 (de) | 2008-10-21 | 2009-05-28 | Cognis Ip Management Gmbh | Kosmetische und/oder pharmazeutische Zubereitungen |
| DE102009031280A1 (de) | 2009-06-30 | 2011-01-05 | Cognis Ip Management Gmbh | Neue Ester und ihre Verwendung |
| ES2744150T3 (es) * | 2009-06-30 | 2020-02-21 | Cognis Ip Man Gmbh | Mezclas de ésteres y composiciones que comprenden tales mezclas de ésteres |
| EP2448907A2 (de) * | 2009-06-30 | 2012-05-09 | Cognis IP Management GmbH | Neue ester und ihre verwendung |
| EP2269566A1 (en) * | 2009-06-30 | 2011-01-05 | Cognis IP Management GmbH | Ester mixtures and compositions comprising such ester mixtures |
| EP2269567A1 (en) * | 2009-06-30 | 2011-01-05 | Cognis IP Management GmbH | Ester mixtures and compositions comprising such ester mixtures |
| CN102665648B (zh) * | 2009-12-22 | 2015-05-20 | 雅芳产品公司 | 稳定化的油包甘油型乳液 |
| DE102010010985B4 (de) * | 2010-03-10 | 2017-09-07 | Emery Oleochemicals Gmbh | Zusammensetzungen enthaltend Fettsäure-2-Propylheptylester und die Verwendung von Fettsäure-2-Propylheptylestern in Herstellungsverfahren und als Viskositätsmodifizierer |
| EP2426101A1 (de) * | 2010-08-05 | 2012-03-07 | Cognis IP Management GmbH | Kosmetische Zubereitungen |
| GB201021937D0 (en) | 2010-12-24 | 2011-02-02 | Reckitt & Colman Overseas | Skin sanitizer compositions comprising alcohol based emulsion |
| WO2012175942A2 (en) | 2011-06-20 | 2012-12-27 | Reckitt & Colman (Overseas) Limited | Foaming topical antimicrobial cleaning compositions |
| US20140341828A1 (en) * | 2011-08-31 | 2014-11-20 | Natura Cosméticos S.A | Cosmetic Composition Intended for Making Up the Skin, and Article Comprising Said Composition |
| GB201122220D0 (en) * | 2011-12-23 | 2012-02-01 | Croda Int Plc | Novel emoillients |
| CN111704543A (zh) * | 2014-11-14 | 2020-09-25 | 燿石治疗公司 | 用于制备α,ω-二羧酸封端的二烷醚的方法和中间体 |
| KR101781589B1 (ko) * | 2015-10-01 | 2017-09-25 | (주)삼경코스텍 | 식물성 오일의 효소 반응 조성물을 함유하는 화장료 조성물 |
| JP6630606B2 (ja) * | 2016-03-23 | 2020-01-15 | クローダジャパン株式会社 | 化粧品組成物 |
| KR101983569B1 (ko) * | 2017-10-26 | 2019-05-29 | 리봄화장품 주식회사 | 동백씨오일 아미노프로판디올 아마이드/에스터를 함유한 피부 보습용 화장료 조성물 |
| EP3901130B1 (en) * | 2018-12-20 | 2023-07-12 | New Japan Chemical Co., Ltd. | Lubricating base oil for fluid dynamic bearing |
| US11660260B2 (en) * | 2020-02-29 | 2023-05-30 | L'oreal | Compositions and methods for treating keratinous substrates |
| WO2022175141A1 (en) * | 2021-02-17 | 2022-08-25 | Evonik Operations Gmbh | Aqueous compositions comprising 6-undecanol-esters |
| DE102021133605A1 (de) | 2021-12-17 | 2023-06-22 | Basf Se | Verfahren zur Herstellung von Estern auf Basis von 2-Propylheptanol |
| EP4410771A1 (en) | 2023-02-03 | 2024-08-07 | Basf Se | Organotin free catalysts for transesterification with mono- and polyfunctional alcohols |
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|---|---|---|---|---|
| DE1138756B (de) * | 1957-11-27 | 1962-10-31 | Eastman Kodak Co | Verfahren zur Herstellung von als Weichmacher dienenden Estern des 2-Propylheptanolsmit gesaettigten aliphatischen oder aromatischen Dicarbonsaeuren |
| JPS5524149A (en) * | 1978-08-09 | 1980-02-21 | New Japan Chem Co Ltd | Cosmetic |
| JPS576790A (en) * | 1980-06-13 | 1982-01-13 | Canon Inc | Recording liquid and recording method |
| JPS6124540A (ja) * | 1984-07-14 | 1986-02-03 | Daisan Kasei Kk | イソミリスチルアルコ−ルのカルボン酸誘導体 |
| JPH07157615A (ja) * | 1993-12-10 | 1995-06-20 | Mitsubishi Chem Corp | 可塑剤組成物 |
| JPH07278056A (ja) * | 1994-04-12 | 1995-10-24 | Mitsubishi Chem Corp | 有機酸エステルの製造方法 |
| DE4420516C2 (de) | 1994-06-13 | 1998-10-22 | Henkel Kgaa | Polyglycerinpolyhydroxystearate |
| US5488121A (en) * | 1994-10-31 | 1996-01-30 | Siltech Inc. | Di-guerbet esters |
| US5639791A (en) * | 1994-10-31 | 1997-06-17 | Siltech Inc | Di-guerbet esters in personal care applications |
| JP3526330B2 (ja) * | 1994-11-15 | 2004-05-10 | 花王株式会社 | 皮膚化粧料 |
| US5849276A (en) | 1996-12-20 | 1998-12-15 | Procter & Gamble | Antiperspirant gel-solid stick compositions containing select nucleating agents |
| DE19742275A1 (de) * | 1997-09-25 | 1999-04-01 | Beiersdorf Ag | Estern verzweigtkettiger Carbonsäuren und verzweigtkettiger Alkohole als antibakterielle, antimycotische, antiparasitäre oder antivirale Wirkstoffe |
| FR2776509B1 (fr) * | 1998-03-31 | 2001-08-10 | Oreal | Composition topique contenant un ester d'acide ou d'alcool gras ramifie en c24 a c28 |
| DE19926671A1 (de) * | 1999-06-11 | 2000-12-14 | Wella Ag | Wasserfreie gelförmige Zusammensetzung |
| DE19939566C1 (de) | 1999-08-20 | 2001-04-05 | Cognis Deutschland Gmbh | Verzweigte, weitgehend ungesättigte Esteröle, Verfahren zu ihrer Herstellung und ihre Verwendung zur Herstellung von kosmetischen und/oder pharmazeutischen Zubereitungen |
| DE10050788A1 (de) | 2000-10-13 | 2002-04-18 | Basf Ag | Zusammensetzung zur Herstellung schwerbenetzbarer Oberflächen |
| 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 |
| DE10305562A1 (de) | 2003-02-10 | 2004-08-26 | Sasol Germany Gmbh | Estermischungen auf Basis verzweigter Alkohole und/oder verzweigter Säuren und deren Verwendung als Polymeradditiv |
-
2006
- 2006-03-09 US US11/886,623 patent/US8642652B2/en active Active
- 2006-03-09 EP EP06723302.3A patent/EP1858480B3/de active Active
- 2006-03-09 JP JP2008501201A patent/JP5275020B2/ja active Active
- 2006-03-09 KR KR1020077021194A patent/KR101330963B1/ko active Active
- 2006-03-09 WO PCT/EP2006/002148 patent/WO2006097235A1/de not_active Ceased
- 2006-03-09 CN CN2006800085713A patent/CN101141944B/zh active Active
- 2006-03-09 ES ES06723302T patent/ES2424750T7/es active Active
-
2014
- 2014-01-07 US US14/149,244 patent/US9314414B2/en active Active
- 2014-01-07 US US14/149,233 patent/US9314413B2/en active Active
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