JP2011525176A5 - - Google Patents
Download PDFInfo
- Publication number
- JP2011525176A5 JP2011525176A5 JP2011512880A JP2011512880A JP2011525176A5 JP 2011525176 A5 JP2011525176 A5 JP 2011525176A5 JP 2011512880 A JP2011512880 A JP 2011512880A JP 2011512880 A JP2011512880 A JP 2011512880A JP 2011525176 A5 JP2011525176 A5 JP 2011525176A5
- Authority
- JP
- Japan
- Prior art keywords
- residues
- oil
- residue
- linear
- acid
- 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
- -1 iso-octyl residue Chemical group 0.000 description 12
- 239000003921 oil Substances 0.000 description 10
- 235000019198 oils Nutrition 0.000 description 10
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 8
- 150000001735 carboxylic acids Chemical class 0.000 description 8
- 235000014113 dietary fatty acids Nutrition 0.000 description 7
- 229930195729 fatty acid Natural products 0.000 description 7
- 239000000194 fatty acid Substances 0.000 description 7
- WWZKQHOCKIZLMA-UHFFFAOYSA-N octanoic acid Chemical compound CCCCCCCC(O)=O WWZKQHOCKIZLMA-UHFFFAOYSA-N 0.000 description 7
- 150000004665 fatty acids Chemical class 0.000 description 6
- 229930006000 Sucrose Natural products 0.000 description 5
- CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 description 5
- 150000002148 esters Chemical class 0.000 description 5
- 239000005720 sucrose Substances 0.000 description 5
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 4
- HVYWMOMLDIMFJA-DPAQBDIFSA-N cholesterol Chemical compound C1C=C2C[C@@H](O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@H]([C@H](C)CCCC(C)C)[C@@]1(C)CC2 HVYWMOMLDIMFJA-DPAQBDIFSA-N 0.000 description 4
- 239000003549 soybean oil Substances 0.000 description 4
- 235000012424 soybean oil Nutrition 0.000 description 4
- 239000005635 Caprylic acid (CAS 124-07-2) Substances 0.000 description 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 3
- 150000002191 fatty alcohols Chemical class 0.000 description 3
- 229960002446 octanoic acid Drugs 0.000 description 3
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 3
- 150000003626 triacylglycerols Chemical class 0.000 description 3
- VLPFTAMPNXLGLX-UHFFFAOYSA-N trioctanoin Chemical compound CCCCCCCC(=O)OCC(OC(=O)CCCCCCC)COC(=O)CCCCCCC VLPFTAMPNXLGLX-UHFFFAOYSA-N 0.000 description 3
- YIWUKEYIRIRTPP-UHFFFAOYSA-N 2-ethylhexan-1-ol Chemical compound CCCCC(CC)CO YIWUKEYIRIRTPP-UHFFFAOYSA-N 0.000 description 2
- IZHVBANLECCAGF-UHFFFAOYSA-N 2-hydroxy-3-(octadecanoyloxy)propyl octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(O)COC(=O)CCCCCCCCCCCCCCCCC IZHVBANLECCAGF-UHFFFAOYSA-N 0.000 description 2
- BANXPJUEBPWEOT-UHFFFAOYSA-N 2-methyl-Pentadecane Chemical compound CCCCCCCCCCCCCC(C)C BANXPJUEBPWEOT-UHFFFAOYSA-N 0.000 description 2
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- WQZGKKKJIJFFOK-PHYPRBDBSA-N alpha-D-galactose Chemical compound OC[C@H]1O[C@H](O)[C@H](O)[C@@H](O)[C@H]1O WQZGKKKJIJFFOK-PHYPRBDBSA-N 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- 235000012000 cholesterol Nutrition 0.000 description 2
- 150000002009 diols Chemical class 0.000 description 2
- SNRUBQQJIBEYMU-UHFFFAOYSA-N dodecane Chemical compound CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 2
- 229930182830 galactose Natural products 0.000 description 2
- DCAYPVUWAIABOU-UHFFFAOYSA-N hexadecane Chemical compound CCCCCCCCCCCCCCCC DCAYPVUWAIABOU-UHFFFAOYSA-N 0.000 description 2
- 150000002430 hydrocarbons Chemical group 0.000 description 2
- GLDOVTGHNKAZLK-UHFFFAOYSA-N octadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCO GLDOVTGHNKAZLK-UHFFFAOYSA-N 0.000 description 2
- 229940049964 oleate Drugs 0.000 description 2
- SSZBUIDZHHWXNJ-UHFFFAOYSA-N palmityl stearate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCCCCCCCCCCCCCCCC SSZBUIDZHHWXNJ-UHFFFAOYSA-N 0.000 description 2
- 229920000728 polyester Polymers 0.000 description 2
- 239000000600 sorbitol Substances 0.000 description 2
- PRAKJMSDJKAYCZ-UHFFFAOYSA-N squalane Chemical compound CC(C)CCCC(C)CCCC(C)CCCCC(C)CCCC(C)CCCC(C)C PRAKJMSDJKAYCZ-UHFFFAOYSA-N 0.000 description 2
- 239000001993 wax Substances 0.000 description 2
- OYHQOLUKZRVURQ-NTGFUMLPSA-N (9Z,12Z)-9,10,12,13-tetratritiooctadeca-9,12-dienoic acid Chemical compound C(CCCCCCC\C(=C(/C\C(=C(/CCCCC)\[3H])\[3H])\[3H])\[3H])(=O)O OYHQOLUKZRVURQ-NTGFUMLPSA-N 0.000 description 1
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 1
- URSCRKIYUPROKB-PHHCKKAISA-N (Z)-octadec-9-enoic acid (2R,3S,4R,5R)-2,3,4,5,6-pentahydroxyhexanal Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C=O.CCCCCCCC\C=C/CCCCCCCC(O)=O.CCCCCCCC\C=C/CCCCCCCC(O)=O.CCCCCCCC\C=C/CCCCCCCC(O)=O.CCCCCCCC\C=C/CCCCCCCC(O)=O URSCRKIYUPROKB-PHHCKKAISA-N 0.000 description 1
- DMBUODUULYCPAK-UHFFFAOYSA-N 1,3-bis(docosanoyloxy)propan-2-yl docosanoate Chemical compound CCCCCCCCCCCCCCCCCCCCCC(=O)OCC(OC(=O)CCCCCCCCCCCCCCCCCCCCC)COC(=O)CCCCCCCCCCCCCCCCCCCCC DMBUODUULYCPAK-UHFFFAOYSA-N 0.000 description 1
- VBICKXHEKHSIBG-UHFFFAOYSA-N 1-monostearoylglycerol Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(O)CO VBICKXHEKHSIBG-UHFFFAOYSA-N 0.000 description 1
- XDOFQFKRPWOURC-UHFFFAOYSA-N 16-methylheptadecanoic acid Chemical compound CC(C)CCCCCCCCCCCCCCC(O)=O XDOFQFKRPWOURC-UHFFFAOYSA-N 0.000 description 1
- 229940043268 2,2,4,4,6,8,8-heptamethylnonane Drugs 0.000 description 1
- ZFFMLCVRJBZUDZ-UHFFFAOYSA-N 2,3-dimethylbutane Chemical group CC(C)C(C)C ZFFMLCVRJBZUDZ-UHFFFAOYSA-N 0.000 description 1
- FLPJVCMIKUWSDR-UHFFFAOYSA-N 2-(4-formylphenoxy)acetamide Chemical compound NC(=O)COC1=CC=C(C=O)C=C1 FLPJVCMIKUWSDR-UHFFFAOYSA-N 0.000 description 1
- SFAAOBGYWOUHLU-UHFFFAOYSA-N 2-ethylhexyl hexadecanoate Chemical compound CCCCCCCCCCCCCCCC(=O)OCC(CC)CCCC SFAAOBGYWOUHLU-UHFFFAOYSA-N 0.000 description 1
- GTJOHISYCKPIMT-UHFFFAOYSA-N 2-methylundecane Chemical compound CCCCCCCCCC(C)C GTJOHISYCKPIMT-UHFFFAOYSA-N 0.000 description 1
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 1
- HBTAOSGHCXUEKI-UHFFFAOYSA-N 4-chloro-n,n-dimethyl-3-nitrobenzenesulfonamide Chemical compound CN(C)S(=O)(=O)C1=CC=C(Cl)C([N+]([O-])=O)=C1 HBTAOSGHCXUEKI-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
- PBWGCNFJKNQDGV-UHFFFAOYSA-N 6-phenylimidazo[2,1-b][1,3]thiazol-5-amine Chemical compound N1=C2SC=CN2C(N)=C1C1=CC=CC=C1 PBWGCNFJKNQDGV-UHFFFAOYSA-N 0.000 description 1
- KGKQNDQDVZQTAG-UHFFFAOYSA-N 8-methylnonyl 2,2-dimethylpropanoate Chemical compound CC(C)CCCCCCCOC(=O)C(C)(C)C KGKQNDQDVZQTAG-UHFFFAOYSA-N 0.000 description 1
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 1
- 244000144725 Amygdalus communis Species 0.000 description 1
- 235000011437 Amygdalus communis Nutrition 0.000 description 1
- 241000272814 Anser sp. Species 0.000 description 1
- 235000000832 Ayote Nutrition 0.000 description 1
- DLQDPUCZIABCES-VZBBZXSKSA-N CCCCC\C=C/C\C=C/CCCCCCCC(=O)OC[C@@H](OC(=O)CCCCCCC\C=C/C\C=C/CCCCC)[C@H](OC(=O)CCCCCCC\C=C/C\C=C/CCCCC)[C@@H](OC(=O)CCCCCCC\C=C/C\C=C/CCCCC)C=O Chemical compound CCCCC\C=C/C\C=C/CCCCCCCC(=O)OC[C@@H](OC(=O)CCCCCCC\C=C/C\C=C/CCCCC)[C@H](OC(=O)CCCCCCC\C=C/C\C=C/CCCCC)[C@@H](OC(=O)CCCCCCC\C=C/C\C=C/CCCCC)C=O DLQDPUCZIABCES-VZBBZXSKSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- 240000004244 Cucurbita moschata Species 0.000 description 1
- 235000009854 Cucurbita moschata Nutrition 0.000 description 1
- 235000009804 Cucurbita pepo subsp pepo Nutrition 0.000 description 1
- WQZGKKKJIJFFOK-QTVWNMPRSA-N D-mannopyranose Chemical compound OC[C@H]1OC(O)[C@@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-QTVWNMPRSA-N 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- FPVVYTCTZKCSOJ-UHFFFAOYSA-N Ethylene glycol distearate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCCOC(=O)CCCCCCCCCCCCCCCCC FPVVYTCTZKCSOJ-UHFFFAOYSA-N 0.000 description 1
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 1
- SHBUUTHKGIVMJT-UHFFFAOYSA-N Hydroxystearate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OO SHBUUTHKGIVMJT-UHFFFAOYSA-N 0.000 description 1
- SGVYKUFIHHTIFL-UHFFFAOYSA-N Isobutylhexyl Natural products CCCCCCCC(C)C SGVYKUFIHHTIFL-UHFFFAOYSA-N 0.000 description 1
- 239000004166 Lanolin Substances 0.000 description 1
- 235000019493 Macadamia oil Nutrition 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- GWFGDXZQZYMSMJ-UHFFFAOYSA-N Octadecansaeure-heptadecylester Natural products CCCCCCCCCCCCCCCCCOC(=O)CCCCCCCCCCCCCCCCC GWFGDXZQZYMSMJ-UHFFFAOYSA-N 0.000 description 1
- 239000005642 Oleic acid Substances 0.000 description 1
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 1
- 240000007594 Oryza sativa Species 0.000 description 1
- 235000007164 Oryza sativa Nutrition 0.000 description 1
- ORCOYXWXSGOGCU-JRMULXMRSA-N P(=O)(O)(O)O.C(CCCCCCC\C=C/CCCCCCCC)(=O)O.C(CCCCCCC\C=C/CCCCCCCC)(=O)O.C(CCCCCCC\C=C/CCCCCCCC)(=O)O.C(CCCCCCC\C=C/CCCCCCCC)(=O)O.C(CCCCCCC\C=C/CCCCCCCC)(=O)O Chemical compound P(=O)(O)(O)O.C(CCCCCCC\C=C/CCCCCCCC)(=O)O.C(CCCCCCC\C=C/CCCCCCCC)(=O)O.C(CCCCCCC\C=C/CCCCCCCC)(=O)O.C(CCCCCCC\C=C/CCCCCCCC)(=O)O.C(CCCCCCC\C=C/CCCCCCCC)(=O)O ORCOYXWXSGOGCU-JRMULXMRSA-N 0.000 description 1
- 235000019483 Peanut oil Nutrition 0.000 description 1
- 235000019484 Rapeseed oil Nutrition 0.000 description 1
- MTCFGRXMJLQNBG-UHFFFAOYSA-N Serine Natural products OCC(N)C(O)=O MTCFGRXMJLQNBG-UHFFFAOYSA-N 0.000 description 1
- 235000019486 Sunflower oil Nutrition 0.000 description 1
- 235000019498 Walnut oil Nutrition 0.000 description 1
- XPXWDKLKEOUSOD-UHRUCXANSA-N [(2S,4R)-2,3,4,5-tetrakis[[(Z)-octadec-9-enoyl]oxy]pentyl] (Z)-octadec-9-enoate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OC[C@@H](OC(=O)CCCCCCC\C=C/CCCCCCCC)C(OC(=O)CCCCCCC\C=C/CCCCCCCC)[C@H](COC(=O)CCCCCCC\C=C/CCCCCCCC)OC(=O)CCCCCCC\C=C/CCCCCCCC XPXWDKLKEOUSOD-UHRUCXANSA-N 0.000 description 1
- 125000002877 alkyl aryl group Chemical group 0.000 description 1
- 239000008168 almond oil Substances 0.000 description 1
- 239000010477 apricot oil Substances 0.000 description 1
- PYMYPHUHKUWMLA-WDCZJNDASA-N arabinose Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)C=O PYMYPHUHKUWMLA-WDCZJNDASA-N 0.000 description 1
- PYMYPHUHKUWMLA-UHFFFAOYSA-N arabinose Natural products OCC(O)C(O)C(O)C=O PYMYPHUHKUWMLA-UHFFFAOYSA-N 0.000 description 1
- 125000003710 aryl alkyl group Chemical group 0.000 description 1
- 239000008163 avocado oil Substances 0.000 description 1
- 235000021302 avocado oil Nutrition 0.000 description 1
- OGBUMNBNEWYMNJ-UHFFFAOYSA-N batilol Chemical class CCCCCCCCCCCCCCCCCCOCC(O)CO OGBUMNBNEWYMNJ-UHFFFAOYSA-N 0.000 description 1
- 235000013871 bee wax Nutrition 0.000 description 1
- 235000015278 beef Nutrition 0.000 description 1
- 239000012166 beeswax Substances 0.000 description 1
- 229940090958 behenyl behenate Drugs 0.000 description 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
- SRBFZHDQGSBBOR-UHFFFAOYSA-N beta-D-Pyranose-Lyxose Natural products OC1COC(O)C(O)C1O SRBFZHDQGSBBOR-UHFFFAOYSA-N 0.000 description 1
- WQZGKKKJIJFFOK-VFUOTHLCSA-N beta-D-glucose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 description 1
- ROPXFXOUUANXRR-YPKPFQOOSA-N bis(2-ethylhexyl) (z)-but-2-enedioate Chemical compound CCCCC(CC)COC(=O)\C=C/C(=O)OCC(CC)CCCC ROPXFXOUUANXRR-YPKPFQOOSA-N 0.000 description 1
- ZFMQKOWCDKKBIF-UHFFFAOYSA-N bis(3,5-difluorophenyl)phosphane Chemical compound FC1=CC(F)=CC(PC=2C=C(F)C=C(F)C=2)=C1 ZFMQKOWCDKKBIF-UHFFFAOYSA-N 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 239000004359 castor oil Substances 0.000 description 1
- 235000019438 castor oil Nutrition 0.000 description 1
- 229940074979 cetyl palmitate Drugs 0.000 description 1
- 229940048851 cetyl ricinoleate Drugs 0.000 description 1
- 239000003240 coconut oil Substances 0.000 description 1
- 235000019864 coconut oil Nutrition 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 235000005687 corn oil Nutrition 0.000 description 1
- 239000002285 corn oil Substances 0.000 description 1
- 125000000753 cycloalkyl group Chemical group 0.000 description 1
- 125000000582 cycloheptyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 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
- 150000001991 dicarboxylic acids Chemical class 0.000 description 1
- 229940031578 diisopropyl adipate Drugs 0.000 description 1
- 229940031569 diisopropyl sebacate Drugs 0.000 description 1
- 239000000539 dimer Substances 0.000 description 1
- TVWTZAGVNBPXHU-FOCLMDBBSA-N dioctyl (e)-but-2-enedioate Chemical compound CCCCCCCCOC(=O)\C=C\C(=O)OCCCCCCCC TVWTZAGVNBPXHU-FOCLMDBBSA-N 0.000 description 1
- MIMDHDXOBDPUQW-UHFFFAOYSA-N dioctyl decanedioate Chemical compound CCCCCCCCOC(=O)CCCCCCCCC(=O)OCCCCCCCC MIMDHDXOBDPUQW-UHFFFAOYSA-N 0.000 description 1
- XFKBBSZEQRFVSL-UHFFFAOYSA-N dipropan-2-yl decanedioate Chemical compound CC(C)OC(=O)CCCCCCCCC(=O)OC(C)C XFKBBSZEQRFVSL-UHFFFAOYSA-N 0.000 description 1
- 125000003438 dodecyl 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
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 235000019197 fats Nutrition 0.000 description 1
- 239000008103 glucose Substances 0.000 description 1
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 1
- 229940074045 glyceryl distearate Drugs 0.000 description 1
- 229940075529 glyceryl stearate Drugs 0.000 description 1
- 239000008169 grapeseed oil Substances 0.000 description 1
- 125000003187 heptyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- IPCSVZSSVZVIGE-UHFFFAOYSA-M hexadecanoate Chemical compound CCCCCCCCCCCCCCCC([O-])=O IPCSVZSSVZVIGE-UHFFFAOYSA-M 0.000 description 1
- PXDJXZJSCPSGGI-UHFFFAOYSA-N hexadecanoic acid hexadecyl ester Natural products CCCCCCCCCCCCCCCCOC(=O)CCCCCCCCCCCCCCC PXDJXZJSCPSGGI-UHFFFAOYSA-N 0.000 description 1
- XAMHKORMKJIEFW-AYTKPMRMSA-N hexadecyl (z,12r)-12-hydroxyoctadec-9-enoate Chemical compound CCCCCCCCCCCCCCCCOC(=O)CCCCCCC\C=C/C[C@H](O)CCCCCC XAMHKORMKJIEFW-AYTKPMRMSA-N 0.000 description 1
- DWMMZQMXUWUJME-UHFFFAOYSA-N hexadecyl octanoate Chemical compound CCCCCCCCCCCCCCCCOC(=O)CCCCCCC DWMMZQMXUWUJME-UHFFFAOYSA-N 0.000 description 1
- IIRDTKBZINWQAW-UHFFFAOYSA-N hexaethylene glycol Chemical compound OCCOCCOCCOCCOCCOCCO IIRDTKBZINWQAW-UHFFFAOYSA-N 0.000 description 1
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 229920006007 hydrogenated polyisobutylene Polymers 0.000 description 1
- 229940072106 hydroxystearate Drugs 0.000 description 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
- VKPSKYDESGTTFR-UHFFFAOYSA-N isododecane Natural products CC(C)(C)CC(C)CC(C)(C)C VKPSKYDESGTTFR-UHFFFAOYSA-N 0.000 description 1
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
- KUVMKLCGXIYSNH-UHFFFAOYSA-N isopentadecane Natural products CCCCCCCCCCCCC(C)C KUVMKLCGXIYSNH-UHFFFAOYSA-N 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 229940074928 isopropyl myristate Drugs 0.000 description 1
- XUGNVMKQXJXZCD-UHFFFAOYSA-N isopropyl palmitate Chemical compound CCCCCCCCCCCCCCCC(=O)OC(C)C XUGNVMKQXJXZCD-UHFFFAOYSA-N 0.000 description 1
- 229940075495 isopropyl palmitate Drugs 0.000 description 1
- 229940119170 jojoba wax Drugs 0.000 description 1
- 235000019388 lanolin Nutrition 0.000 description 1
- 229940039717 lanolin Drugs 0.000 description 1
- 239000010469 macadamia oil Substances 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 239000004200 microcrystalline wax Substances 0.000 description 1
- 235000019808 microcrystalline wax Nutrition 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 239000001788 mono and diglycerides of fatty acids Substances 0.000 description 1
- 229940078812 myristyl myristate Drugs 0.000 description 1
- 229940078555 myristyl propionate Drugs 0.000 description 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- GOQYKNQRPGWPLP-UHFFFAOYSA-N n-heptadecyl alcohol Natural products CCCCCCCCCCCCCCCCCO GOQYKNQRPGWPLP-UHFFFAOYSA-N 0.000 description 1
- 125000003136 n-heptyl 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])* 0.000 description 1
- 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000001624 naphthyl group Chemical group 0.000 description 1
- 125000001971 neopentyl group Chemical group [H]C([*])([H])C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 125000001400 nonyl 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])C([H])([H])[H] 0.000 description 1
- NKBWPOSQERPBFI-UHFFFAOYSA-N octadecyl octadecanoate Chemical compound CCCCCCCCCCCCCCCCCCOC(=O)CCCCCCCCCCCCCCCCC NKBWPOSQERPBFI-UHFFFAOYSA-N 0.000 description 1
- 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 description 1
- 239000004006 olive oil Substances 0.000 description 1
- 235000008390 olive oil Nutrition 0.000 description 1
- 125000001037 p-tolyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])([H])[H] 0.000 description 1
- 125000000913 palmityl 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])C([H])([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 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 235000019809 paraffin wax Nutrition 0.000 description 1
- 239000000312 peanut oil Substances 0.000 description 1
- 235000019271 petrolatum Nutrition 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- BFZNCPXNOGIELB-UHFFFAOYSA-N propan-2-yl 10-[5,6-dihexyl-2-(8-oxo-8-propan-2-yloxyoctyl)cyclohex-3-en-1-yl]dec-9-enoate Chemical compound CCCCCCC1C=CC(CCCCCCCC(=O)OC(C)C)C(C=CCCCCCCCC(=O)OC(C)C)C1CCCCCC BFZNCPXNOGIELB-UHFFFAOYSA-N 0.000 description 1
- 235000015136 pumpkin Nutrition 0.000 description 1
- 235000009566 rice Nutrition 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 239000008159 sesame oil Substances 0.000 description 1
- 235000011803 sesame oil Nutrition 0.000 description 1
- 239000000779 smoke Substances 0.000 description 1
- 235000000346 sugar Nutrition 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- 239000002600 sunflower oil Substances 0.000 description 1
- 239000003760 tallow Substances 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
- 125000001973 tert-pentyl group Chemical group [H]C([H])([H])C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- YRZGMTHQPGNLEK-UHFFFAOYSA-N tetradecyl propionate Chemical compound CCCCCCCCCCCCCCOC(=O)CC YRZGMTHQPGNLEK-UHFFFAOYSA-N 0.000 description 1
- DZKXJUASMGQEMA-UHFFFAOYSA-N tetradecyl tetradecanoate Chemical compound CCCCCCCCCCCCCCOC(=O)CCCCCCCCCCCCC DZKXJUASMGQEMA-UHFFFAOYSA-N 0.000 description 1
- 239000013638 trimer Substances 0.000 description 1
- 239000008170 walnut oil Substances 0.000 description 1
- 125000005023 xylyl group Chemical group 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP08010779.0 | 2008-06-13 | ||
| EP08010779A EP1972330B1 (en) | 2008-06-13 | 2008-06-13 | Cosmetic or pharmaceutical compositions comprising modified polysiloxanes with at least one carbamate group |
| PCT/EP2009/004090 WO2009149879A1 (en) | 2008-06-13 | 2009-06-06 | Cosmetic or pharmaceutical compositions comprising modified polysiloxanes with at least one carbamate group |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2011525176A JP2011525176A (ja) | 2011-09-15 |
| JP2011525176A5 true JP2011525176A5 (enExample) | 2012-07-26 |
| JP5531012B2 JP5531012B2 (ja) | 2014-06-25 |
Family
ID=39683909
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2011512880A Expired - Fee Related JP5531012B2 (ja) | 2008-06-13 | 2009-06-06 | 少なくとも１個のカルバマート基を有する変性ポリシロキサン類を含む化粧料組成物または医薬組成物 |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US20110104085A1 (enExample) |
| EP (1) | EP1972330B1 (enExample) |
| JP (1) | JP5531012B2 (enExample) |
| CN (1) | CN102065835B (enExample) |
| ES (1) | ES2391913T3 (enExample) |
| WO (1) | WO2009149879A1 (enExample) |
Families Citing this family (44)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| MX2011011619A (es) | 2009-05-01 | 2012-02-28 | Signal Invest And Man Co | Composicion antimicrobiana hidratante. |
| DE102009022444A1 (de) * | 2009-05-23 | 2010-01-07 | Clariant International Limited | Zusammensetzung enthaltend Sorbitanmonocaprylat und antimikrobielle Wirkstoffe |
| DE102009022445A1 (de) | 2009-05-23 | 2009-12-24 | Clariant International Limited | Zusammensetzung enthaltend Sorbitanmonocaprylat und Alkohol |
| WO2011137563A1 (en) * | 2010-05-07 | 2011-11-10 | Unilever Plc | High solvent content emulsions |
| DE102010062156A1 (de) | 2010-10-25 | 2012-04-26 | Evonik Goldschmidt Gmbh | Polysiloxane mit stickstoffhaltigen Gruppen |
| DE102010062676A1 (de) | 2010-12-09 | 2012-06-14 | Evonik Goldschmidt Gmbh | Zubereitungen enthaltend Polysiloxane mit stickstoffhaltigen Gruppen |
| JP5908901B2 (ja) * | 2011-01-28 | 2016-04-26 | モメンティブ パフォーマンス マテリアルズ ゲーエムベーハー | Ｕｖ光防御化粧品組成物 |
| US8580285B2 (en) * | 2011-06-09 | 2013-11-12 | Momentive Performance Materials Inc. | Clarifying agents for organomodified silicones |
| US9730450B2 (en) | 2011-08-04 | 2017-08-15 | Clariant International Ltd. | Use of isosorbide monoesters as antimicrobial active substances |
| WO2013017256A1 (de) | 2011-08-04 | 2013-02-07 | Clariant International Ltd | Verwendung von isosorbiddiestern als verdicker |
| EP2739150B1 (de) | 2011-08-04 | 2016-10-19 | Clariant International Ltd | Zusammensetzung enthaltend isosorbidmonoester und isosorbiddiester |
| JP6037574B2 (ja) | 2011-08-04 | 2016-12-07 | クラリアント・インターナシヨナル・リミテツド | イソソルビドモノエステルおよびｎ−ヒドロキシピリドン類を含有する組成物 |
| ES2639115T3 (es) | 2011-08-04 | 2017-10-25 | Clariant International Ltd. | Uso de monoésteres de isosorbida como espesante |
| EP2739152B1 (de) | 2011-08-04 | 2016-09-28 | Clariant International Ltd. | Zusammensetzungen enthaltend isosorbidmonoester und alkohole, die mindestens eine aromatische gruppe enthalten |
| DE102011110100A1 (de) | 2011-08-12 | 2013-02-14 | Evonik Goldschmidt Gmbh | Verfahren zu Herstellungen von Polysiloxanen mit stickstoffhaltigen Gruppen |
| JP5754849B2 (ja) * | 2011-10-11 | 2015-07-29 | 信越化学工業株式会社 | 粉体処理剤、処理粉体及び油中粉体分散物 |
| WO2013082112A1 (en) | 2011-11-29 | 2013-06-06 | Dow Corning Corporation | Aminofunctional silicone emulsions |
| DE102012201167A1 (de) | 2012-01-27 | 2013-08-01 | Evonik Industries Ag | Mischungszusammensetzung enthaltend aminofunktionelle Siloxane, hydrophobePartikel und hochmolekulare Silicone sowie dessen Verwendung zur Lederbehandlung |
| BR112014021199A2 (pt) * | 2012-03-01 | 2018-05-08 | Basf Se | composição, método para preparação da composição, polímero, método para preparação do polímero, método para controlar fungos e semente |
| US8853189B2 (en) | 2012-05-31 | 2014-10-07 | Prima Innovations, Llc | Antispasmodic 1,2-Diols and 1,2,3-triols |
| DE102012222783A1 (de) | 2012-12-11 | 2014-06-12 | Beiersdorf Ag | Polyolhaltige kosmetische oder dermatologische Zubereitungen mit verbesserter Sensorik |
| US10221283B2 (en) * | 2013-01-18 | 2019-03-05 | Georgetown University | Amino-substituted polysiloxanes combined with polymerizable and unpolymerizable organic acids |
| DE102014200106B4 (de) | 2013-02-13 | 2018-04-26 | Evonik Degussa Gmbh | Härtbare organomodifizierte Siloxane hergestellt durch Kondensation |
| US10542750B2 (en) | 2013-07-15 | 2020-01-28 | The Procter & Gamble Company | Cleansing composition having a preservative system and a wet wipe comprising the cleansing composition |
| JP6270266B2 (ja) * | 2014-02-19 | 2018-01-31 | 住友ゴム工業株式会社 | プレフィルドシリンジ用ガスケットおよびプレフィルドシリンジ |
| US10172783B2 (en) * | 2014-06-04 | 2019-01-08 | L'oreal | High UV protection alcohol-free anhydrous clear system |
| EP3197937B1 (en) * | 2014-09-23 | 2024-04-24 | Momentive Performance Materials GmbH | Silicone compounds and compositions thereof for the treatment of amino acid based substrates |
| US10765613B2 (en) | 2014-09-30 | 2020-09-08 | The Procter & Gamble Company | Stable lotion emulsion composition and wet wipe |
| DE102014225430A1 (de) * | 2014-12-10 | 2016-06-16 | Henkel Ag & Co. Kgaa | Mittel und Verfahren zur temporären Verformung von keratinhaltiger Fasern |
| DE102014225443A1 (de) * | 2014-12-10 | 2016-06-16 | Henkel Ag & Co. Kgaa | Mittel und Verfahren zur temporären Verformung keratinhaltiger Fasern |
| CN104530433A (zh) * | 2014-12-18 | 2015-04-22 | 南雄鼎成化工有限公司 | 抗黄变亲水氨基硅油的制备方法 |
| DE102015222074A1 (de) | 2015-11-10 | 2017-05-11 | Beiersdorf Ag | Wirkstoffkombination zur Hautbefeuchtung in Reinigungszubereitungen |
| MX370963B (es) * | 2016-02-19 | 2020-01-10 | Colgate Palmolive Co | Composiciones para el cuidado personal. |
| DE102016207063A1 (de) * | 2016-04-26 | 2017-10-26 | Wacker Chemie Ag | Zusammensetzungen enthaltend Carbamato-funktionalisierte Organopolysiloxane und kationische Tenside |
| DE102016207060A1 (de) | 2016-04-26 | 2017-10-26 | Wacker Chemie Ag | Wässrige Emulsionen aus Carbamato-funktionalisierten Organopolysiloxanen |
| EP4563684A3 (en) | 2017-09-06 | 2025-08-20 | Evonik Operations GmbH | Microemulsion comprising quaternary ammonium compound, especially for production of fabric softener formulations |
| CN111133089B (zh) | 2017-09-25 | 2021-09-28 | 赢创运营有限公司 | 具有改进的储存稳定性的含聚硅氧烷的浓缩物及其优选在纺织品护理组合物中的用途 |
| CN112368362B (zh) | 2018-07-05 | 2022-05-24 | 赢创运营有限公司 | 用于高粘度洗衣清洁制剂的活性组合物 |
| CN109512684B (zh) * | 2018-12-29 | 2021-09-07 | 浙江大学华南工业技术研究院 | 一种高含量二氧化钛或氧化锌的防晒剂及其制备方法 |
| CN110255568B (zh) * | 2019-06-28 | 2022-06-10 | 广西大学 | 一种内外双层胺基改性SiO2气凝胶的合成方法及其应用 |
| MX2022012065A (es) * | 2020-03-31 | 2022-10-13 | Unilever Ip Holdings B V | Metodo para tratamiento del cuero cabelludo. |
| WO2022020332A1 (en) | 2020-07-21 | 2022-01-27 | Chembeau LLC | Diester cosmetic formulations and uses thereof |
| EP4436540A1 (en) | 2021-11-23 | 2024-10-02 | Dow Global Technologies LLC | Silane hydrolyzate and processes for the preparation and use thereof |
| CN114854024B (zh) * | 2022-05-26 | 2023-03-28 | 东华大学 | 一种改性氨基甲酸酯硅油乳液及其制备方法和制备聚丙烯腈碳纤维的方法 |
Family Cites Families (48)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2947771A (en) * | 1956-10-12 | 1960-08-02 | Union Carbide Corp | Aminoalkylpolysiloxanes and process for their production |
| US3355424A (en) * | 1964-07-29 | 1967-11-28 | Dow Corning | Method for the preparation of aminoalkylsiloxane copolymers |
| US4104296A (en) | 1970-09-28 | 1978-08-01 | Union Carbide Corporation | Organofunctional silicon compounds |
| US3890269A (en) * | 1972-08-11 | 1975-06-17 | Stauffer Chemical Co | Process for preparing aminofunctional polysiloxane polymers |
| LU84463A1 (fr) * | 1982-11-10 | 1984-06-13 | Oreal | Polymeres polysiloxanes polyquaternaires |
| EP0116160B1 (de) * | 1983-01-18 | 1987-12-23 | BBC Brown Boveri AG | Aussengelagerter Abgasturbolader mit ungekühltem Gaskanal |
| US4500438A (en) * | 1983-06-24 | 1985-02-19 | American Hoechst Corporation | Multi-ring fluorinated carbamates with textile soil repellent activity |
| JPS61296184A (ja) * | 1985-06-20 | 1986-12-26 | 信越化学工業株式会社 | 繊維処理剤 |
| DE3705121A1 (de) * | 1987-02-18 | 1988-09-01 | Goldschmidt Ag Th | Polyquaternaere polysiloxan-polymere, deren herstellung und verwendung in kosmetischen zubereitungen |
| DE3719086C1 (de) * | 1987-06-06 | 1988-10-27 | Goldschmidt Ag Th | Diquartaere Polysiloxane,deren Herstellung und Verwendung in kosmetischen Zubereitungen |
| US4988504A (en) * | 1987-08-19 | 1991-01-29 | General Electric Company | Silicone surfactants |
| JPH01221580A (ja) * | 1988-02-27 | 1989-09-05 | Shin Etsu Chem Co Ltd | 繊維処理剤 |
| FR2648821A1 (enExample) * | 1989-06-22 | 1990-12-28 | Rhone Poulenc Chimie | |
| DE4004946A1 (de) * | 1990-02-16 | 1991-08-22 | Wacker Chemie Gmbh | Feinteilige organopolysiloxanemulsionen |
| FR2673838B1 (fr) * | 1991-03-14 | 1995-03-03 | Oreal | Compositions cosmetiques contenant une dispersion de particules solides dont la surface est revetue a l'aide d'un polymere cationique. |
| US5389364A (en) * | 1993-08-06 | 1995-02-14 | Dow Corning Corporation | Conditioning hair with aminosilane reaction products with lactones or carbonates |
| DE4426794C1 (de) * | 1994-07-28 | 1995-07-06 | Goldwell Ag | Mittel zur Haarbehandlung |
| US5672338A (en) | 1996-03-14 | 1997-09-30 | General Electric Company | Cosmetic compositions made with hydroxy carbamate functionalized silicones |
| US5725736A (en) * | 1996-10-25 | 1998-03-10 | Kimberly-Clark Worldwide, Inc. | Tissue containing silicone betaines |
| BR9811710A (pt) | 1997-06-23 | 2000-08-29 | Procter & Gamble | Composições desodorantes em gel tendo nìvel reduzido de irritação na pele |
| BR9812101A (pt) * | 1997-07-17 | 2000-07-18 | Bioshield Technologies Inc | Compostos de organossilano e uso dos mesmos |
| US6132739A (en) | 1998-09-01 | 2000-10-17 | Amway Corporation | Makeup compositions and methods of making same |
| US6130579A (en) * | 1999-03-29 | 2000-10-10 | Rf Micro Devices, Inc. | Feed-forward biasing for RF amplifiers |
| DE19928127C1 (de) * | 1999-06-19 | 2000-05-31 | Clariant Gmbh | Antimikrobielle Siloxanquat-Formulierungen, deren Herstellung und Verwendung |
| US6289274B1 (en) * | 1999-08-13 | 2001-09-11 | United Technologies Corporation | Fuzzy logic based fuel flow selection system |
| US7041767B2 (en) * | 2000-07-27 | 2006-05-09 | Ge Bayer Silicones Gmbh & Co. Kg | Polysiloxane polymers, method for their production and the use thereof |
| EP1258503A1 (de) * | 2001-05-15 | 2002-11-20 | Clariant International Ltd. | Modifizierte Polyorganosiloxane, wässrige Emulsionen davon, ihre Herstellung und Verwendung |
| US6482969B1 (en) * | 2001-10-24 | 2002-11-19 | Dow Corning Corporation | Silicon based quaternary ammonium functional compositions and methods for making them |
| US20030082128A1 (en) * | 2001-10-24 | 2003-05-01 | Clariant International, Ltd. | Homogeneous mixtures of silicone oils and organic oils |
| US7235230B2 (en) * | 2001-10-24 | 2007-06-26 | Clariant Finance (Bvi) Limited | Leave-on compositions for personal care |
| DE10163242A1 (de) * | 2001-12-21 | 2003-07-10 | Clariant Gmbh | Deodorantien und Antiperspirantien |
| BR0308602B1 (pt) * | 2002-03-21 | 2013-12-17 | Composições de tratamento capilar compreendendo polissiloxano, e método de condicionamento capilar | |
| US20040042991A1 (en) * | 2002-06-08 | 2004-03-04 | Clariant Gmbh | Single-phase cosmetic care compositions |
| US20030232030A1 (en) * | 2002-06-12 | 2003-12-18 | L'oreal | Compositions containing at least one oil structured with at least one silicone-polyamide polymer, and at least one gelling agent and methods of using the same |
| US6958155B2 (en) * | 2002-06-12 | 2005-10-25 | L'oreal | Cosmetic compositions comprising at least one polysiloxane based polyamide |
| DE10243992A1 (de) * | 2002-09-21 | 2004-04-01 | Goldschmidt Ag | Polyestergruppen aufweisende amphiphile Organopolysiloxane und deren Verwendung als Emulgatoren oder Dispergierhilfsmittel |
| DE10320631A1 (de) * | 2003-05-08 | 2004-12-09 | Wacker-Chemie Gmbh | Polyalkoxyreste aufweisende Organosiliciumverbindungen |
| DE102004013795A1 (de) * | 2004-03-20 | 2004-10-28 | Clariant Gmbh | Kosmetische oder pharmazeutische Mittel, enthaltend modifizierte Polyorganosiloxane |
| WO2008008077A2 (en) | 2005-07-29 | 2008-01-17 | Ndsu Research Foundation | Functionalized polysiloxane polymers |
| DE102005039511A1 (de) * | 2005-08-20 | 2007-02-22 | Clariant Produkte (Deutschland) Gmbh | Verwendung von quaternären Polysiloxanen in Reinigungs- und Pflegemitteln |
| WO2007024792A1 (en) | 2005-08-25 | 2007-03-01 | Henkel Corporation | Rtv silicone compositions using carbamate functional alpha silane crosslinkers |
| KR100777009B1 (ko) | 2005-12-30 | 2007-11-28 | 주식회사 케이씨씨 | 흡습성 폴리실록산 및 그의 제조 방법 |
| DE502007000339D1 (de) * | 2006-05-04 | 2009-02-12 | Wacker Chemie Ag | Verfahren zur Herstellung von Urethangruppen aufweisenden Organosiliciumverbindungen |
| DE102006020815A1 (de) * | 2006-05-04 | 2007-11-08 | Wacker Chemie Ag | Verfahren zur Herstellung von beta-Ketocarbonyl-funktionellen Organosiliciumverbindungen |
| DE102006020818A1 (de) * | 2006-05-04 | 2007-11-08 | Wacker Chemie Ag | Polare Gruppen aufweisende Organopolysiloxane und Verfahren zu deren Herstellung |
| US20080014166A1 (en) * | 2006-07-14 | 2008-01-17 | Clariant International, Ltd. | Cosmetic or pharmaceutical compositions comprising modified polyorganosiloxanes |
| JP2008285538A (ja) * | 2007-05-16 | 2008-11-27 | Konishi Co Ltd | 硬化性樹脂組成物及びそれを用いた接着剤組成物 |
| JP2011522944A (ja) * | 2008-06-13 | 2011-08-04 | クラリアント・ファイナンス・（ビーブイアイ）・リミテッド | カルバマート官能基を有するポリジオルガノシロキサン、それらの調製、および繊維工業における柔軟剤としてのそれらの使用 |
-
2008
- 2008-06-13 EP EP08010779A patent/EP1972330B1/en not_active Not-in-force
- 2008-06-13 ES ES08010779T patent/ES2391913T3/es active Active
-
2009
- 2009-06-06 JP JP2011512880A patent/JP5531012B2/ja not_active Expired - Fee Related
- 2009-06-06 WO PCT/EP2009/004090 patent/WO2009149879A1/en not_active Ceased
- 2009-06-06 US US12/997,460 patent/US20110104085A1/en not_active Abandoned
- 2009-06-06 CN CN2009801217855A patent/CN102065835B/zh not_active Expired - Fee Related
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP2011525176A5 (enExample) | ||
| Shin et al. | Lipid extraction from Tetraselmis sp. microalgae for biodiesel production using hexane-based solvent mixtures | |
| Feltes et al. | The production, benefits, and applications of monoacylglycerols and diacylglycerols of nutritional interest | |
| CN101932717B (zh) | 用于脂肪酸烷基酯合成的强力多酶制剂 | |
| Xu, Wei Du, Jing Zeng and Dehua Liu | Conversion of soybean oil to biodiesel fuel using lipozyme TL IM in a solvent-free medium | |
| Gryglewicz et al. | Enzymatic synthesis of rapeseed oil-based lubricants | |
| López et al. | Production of biodiesel from vegetable oil and microalgae by fatty acid extraction and enzymatic esterification | |
| JP2007531776A5 (enExample) | ||
| JP2010519311A5 (enExample) | ||
| EP2636313B1 (en) | Glyceride composition obtainable from shea oil | |
| JP2010196060A5 (enExample) | ||
| RU2010113506A (ru) | Способ получения твердого масла | |
| JP2009507480A (ja) | ジオレイルパルミトイルグリセリドの製造方法 | |
| ATE188243T1 (de) | Verfahren zur herstellung von fettsäureäthylestern | |
| DK2956010T3 (en) | FAT COMPOSITION | |
| US6143348A (en) | Low saturated fatty acid oils | |
| Mustafa | Lipase catalyzed reactions: a promising approach for clean synthesis of oleochemicals | |
| Kim et al. | Synthesis of α-linolenic acid-rich triacylglycerol using a newly prepared immobilized lipase | |
| JP6715586B2 (ja) | 高度不飽和脂肪酸の製造方法 | |
| WO2002005849A3 (en) | Transportation of nucleic acid substances | |
| US4956287A (en) | Process for producing oleaginous composition | |
| ES2346686T3 (es) | Obtencion de monogliceridos a partir de trigliceridos por alcoholisis con empleo de lipasa de thermomyces lanuginosus, que es activada por medio de sales alcalinas. | |
| Feltes et al. | Assessment of process parameters on the production of diglycerides rich in omega-3 fatty acids through the enzymatic glycerolysis of fish oil | |
| Ju et al. | Efficient synthesis of stearidonic acid enriched triacylglycerol from ahiflower seed oil via a two-step enzyme reaction | |
| JP6645804B2 (ja) | 構造油脂の製造方法 |