ES2205571T3 - Alcoholes grasos insaturados de palma. - Google Patents
Alcoholes grasos insaturados de palma.Info
- Publication number
- ES2205571T3 ES2205571T3 ES98955557T ES98955557T ES2205571T3 ES 2205571 T3 ES2205571 T3 ES 2205571T3 ES 98955557 T ES98955557 T ES 98955557T ES 98955557 T ES98955557 T ES 98955557T ES 2205571 T3 ES2205571 T3 ES 2205571T3
- Authority
- ES
- Spain
- Prior art keywords
- unsaturated
- fatty alcohols
- saturated
- alcohols
- palm
- 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.)
- Expired - Lifetime
Links
- 235000015096 spirit Nutrition 0.000 title 1
- 235000021081 unsaturated fats Nutrition 0.000 title 1
- 150000002191 fatty alcohols Chemical class 0.000 claims abstract description 27
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 claims abstract description 20
- 229910052740 iodine Inorganic materials 0.000 claims abstract description 20
- 239000011630 iodine Substances 0.000 claims abstract description 20
- 238000000034 method Methods 0.000 claims abstract description 10
- 229920006395 saturated elastomer Polymers 0.000 claims abstract description 9
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 8
- 235000014113 dietary fatty acids Nutrition 0.000 claims abstract description 8
- 229930195729 fatty acid Natural products 0.000 claims abstract description 8
- 239000000194 fatty acid Substances 0.000 claims abstract description 8
- 239000003292 glue Substances 0.000 claims abstract description 8
- 150000004702 methyl esters Chemical class 0.000 claims abstract description 8
- 150000004665 fatty acids Chemical class 0.000 claims abstract description 7
- 150000001298 alcohols Chemical class 0.000 claims abstract description 6
- 239000000203 mixture Substances 0.000 claims abstract description 6
- 238000012423 maintenance Methods 0.000 claims abstract description 4
- 229910052799 carbon Inorganic materials 0.000 claims description 5
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 4
- 125000004429 atom Chemical group 0.000 claims description 4
- 239000003925 fat Substances 0.000 claims description 4
- 125000000217 alkyl group Chemical group 0.000 claims description 2
- 125000004417 unsaturated alkyl group Chemical group 0.000 abstract 1
- 239000000047 product Substances 0.000 description 27
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- 238000005984 hydrogenation reaction Methods 0.000 description 6
- 230000006399 behavior Effects 0.000 description 5
- 238000004519 manufacturing process Methods 0.000 description 5
- 239000002994 raw material Substances 0.000 description 5
- 150000002148 esters Chemical class 0.000 description 4
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 3
- 235000019482 Palm oil Nutrition 0.000 description 3
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 3
- 239000003054 catalyst Substances 0.000 description 3
- 229910052804 chromium Inorganic materials 0.000 description 3
- 239000011651 chromium Substances 0.000 description 3
- 235000019197 fats Nutrition 0.000 description 3
- 235000019387 fatty acid methyl ester Nutrition 0.000 description 3
- 239000000945 filler Substances 0.000 description 3
- 230000003647 oxidation Effects 0.000 description 3
- 238000007254 oxidation reaction Methods 0.000 description 3
- 239000002540 palm oil Substances 0.000 description 3
- 235000013311 vegetables Nutrition 0.000 description 3
- 239000011701 zinc Substances 0.000 description 3
- 229910052725 zinc Inorganic materials 0.000 description 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
- 239000004165 Methyl ester of fatty acids Substances 0.000 description 2
- FLIACVVOZYBSBS-UHFFFAOYSA-N Methyl palmitate Chemical compound CCCCCCCCCCCCCCCC(=O)OC FLIACVVOZYBSBS-UHFFFAOYSA-N 0.000 description 2
- 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 2
- 150000001875 compounds Chemical class 0.000 description 2
- 239000002537 cosmetic Substances 0.000 description 2
- 238000004821 distillation Methods 0.000 description 2
- IPCSVZSSVZVIGE-UHFFFAOYSA-N hexadecanoic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- 239000003921 oil Substances 0.000 description 2
- 235000019198 oils Nutrition 0.000 description 2
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- 235000021314 Palmitic acid Nutrition 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 235000012000 cholesterol Nutrition 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 230000008878 coupling Effects 0.000 description 1
- 238000010168 coupling process Methods 0.000 description 1
- 238000005859 coupling reaction Methods 0.000 description 1
- 238000010494 dissociation reaction Methods 0.000 description 1
- 230000005593 dissociations Effects 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 238000005194 fractionation Methods 0.000 description 1
- 238000004817 gas chromatography Methods 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 238000009434 installation Methods 0.000 description 1
- 239000000543 intermediate Substances 0.000 description 1
- 239000013067 intermediate product Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- -1 methyl fatty acids Chemical class 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- WQEPLUUGTLDZJY-UHFFFAOYSA-N n-Pentadecanoic acid Natural products CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-UHFFFAOYSA-N 0.000 description 1
- 238000012856 packing Methods 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 238000003303 reheating Methods 0.000 description 1
- 238000005201 scrubbing Methods 0.000 description 1
- 238000010517 secondary reaction Methods 0.000 description 1
- 238000007711 solidification Methods 0.000 description 1
- 230000008023 solidification Effects 0.000 description 1
- 150000003431 steroids Chemical class 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 239000003760 tallow Substances 0.000 description 1
- 150000003626 triacylglycerols Chemical class 0.000 description 1
- 150000004670 unsaturated fatty acids Chemical class 0.000 description 1
- 235000021122 unsaturated fatty acids Nutrition 0.000 description 1
- 238000011144 upstream manufacturing Methods 0.000 description 1
- 235000019871 vegetable fat Nutrition 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 238000007704 wet chemistry method Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C29/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
- C07C29/132—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of an oxygen containing functional group
- C07C29/136—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of an oxygen containing functional group of >C=O containing groups, e.g. —COOH
- C07C29/147—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of an oxygen containing functional group of >C=O containing groups, e.g. —COOH of carboxylic acids or derivatives thereof
- C07C29/149—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of an oxygen containing functional group of >C=O containing groups, e.g. —COOH of carboxylic acids or derivatives thereof with hydrogen or hydrogen-containing gases
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Fats And Perfumes (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19750800A DE19750800C2 (de) | 1997-11-17 | 1997-11-17 | Verfahren zur Herstellung ungesättigter Palmfettalkohole |
| DE19750800 | 1997-11-17 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES2205571T3 true ES2205571T3 (es) | 2004-05-01 |
Family
ID=7848922
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES98955557T Expired - Lifetime ES2205571T3 (es) | 1997-11-17 | 1998-11-09 | Alcoholes grasos insaturados de palma. |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US7169959B2 (enExample) |
| EP (1) | EP1032552B1 (enExample) |
| JP (1) | JP2001523654A (enExample) |
| DE (2) | DE19750800C2 (enExample) |
| ES (1) | ES2205571T3 (enExample) |
| WO (1) | WO1999025673A1 (enExample) |
Families Citing this family (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE19810440C1 (de) * | 1998-03-11 | 1999-09-23 | Dhw Deutsche Hydrierwerke Gmbh | Verfahren zur Herstellung von ungesättigten Fettalkoholen aus Lauricölen |
| DE19912683C2 (de) * | 1999-03-20 | 2001-07-12 | Cognis Deutschland Gmbh | Verfahren zur Herstellung von Palmfettalkoholen |
| FR2833006A1 (fr) * | 2001-11-30 | 2003-06-06 | Cognis France Sa | Procede de preparation d'ester methylique d'acide oleique industriel |
| JP3680948B2 (ja) * | 2002-04-19 | 2005-08-10 | 新日本理化株式会社 | 液状植物性不飽和アルコール及びその製造方法 |
| CN103013587A (zh) * | 2003-05-14 | 2013-04-03 | 马来西亚棕油局 | 生产棕榈生物柴油的方法 |
| US7524339B2 (en) * | 2003-12-02 | 2009-04-28 | Lumetique, Inc. | Lamp oil composition and lighter fluid composition |
| DE102007027372A1 (de) * | 2007-06-11 | 2008-12-18 | Cognis Oleochemicals Gmbh | Verfahren zur Hydrierung von Glycerin |
| DE102007027371A1 (de) * | 2007-06-11 | 2008-12-18 | Cognis Oleochemicals Gmbh | Verfahren zur Herstellung einer Verbindung aufweisend mindestens eine Ester-Gruppe |
| MY174521A (en) | 2012-04-24 | 2020-04-23 | Stepan Co | Unsaturated fatty alcohol derivatives from natural oil metathesis |
| MY169208A (en) | 2012-04-24 | 2019-03-18 | Stepan Co | Unsaturated fatty alcohol alkoxylates from natural oil metathesis |
| WO2013163071A1 (en) | 2012-04-24 | 2013-10-31 | Elevance Renewable Sciences, Inc. | Unsaturated fatty alcohol compositions and derivatives from natural oil metathesis |
| PL2967033T3 (pl) | 2013-03-13 | 2020-01-31 | Stepan Company | Środki powierzchniowo czynne na bazie jednonienasyconych pochodnych alkoholi tłuszczowych |
| US9266918B2 (en) | 2013-03-14 | 2016-02-23 | Elevance Renewable Sciences, Inc. | Alkenyl glycosides and their preparation |
| CN108697072A (zh) | 2015-11-18 | 2018-10-23 | 普罗维维股份有限公司 | 用于产生昆虫信息素及相关化合物的微生物 |
| WO2017214133A2 (en) * | 2016-06-06 | 2017-12-14 | Provivi, Inc. | Semi-biosynthetic production of fatty alcohols and fatty aldehydes |
| WO2018213554A1 (en) | 2017-05-17 | 2018-11-22 | Provivi, Inc. | Microorganisms for the production of insect pheromones and related compounds |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE4335781C2 (de) * | 1993-10-20 | 1998-02-19 | Henkel Kgaa | Fettalkohole auf pflanzlicher Basis und Verfahren zu Ihrer Herstellung |
| DE4425180C2 (de) * | 1994-07-16 | 1997-05-07 | Henkel Kgaa | Verfahren zur Herstellung ungesättigter Fettalkohole oder deren veresterte, alkoxylierte und/oder sulfatierte Derivate mit verbessertem Kälteverhalten |
-
1997
- 1997-11-17 DE DE19750800A patent/DE19750800C2/de not_active Expired - Fee Related
-
1998
- 1998-11-09 DE DE59809229T patent/DE59809229D1/de not_active Expired - Lifetime
- 1998-11-09 EP EP98955557A patent/EP1032552B1/de not_active Expired - Lifetime
- 1998-11-09 ES ES98955557T patent/ES2205571T3/es not_active Expired - Lifetime
- 1998-11-09 WO PCT/EP1998/007148 patent/WO1999025673A1/de not_active Ceased
- 1998-11-09 JP JP2000521060A patent/JP2001523654A/ja active Pending
-
2001
- 2001-06-12 US US09/880,695 patent/US7169959B2/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| DE19750800A1 (de) | 1999-05-27 |
| JP2001523654A (ja) | 2001-11-27 |
| EP1032552A1 (de) | 2000-09-06 |
| US20020037932A1 (en) | 2002-03-28 |
| DE19750800C2 (de) | 2001-04-26 |
| DE59809229D1 (de) | 2003-09-11 |
| US7169959B2 (en) | 2007-01-30 |
| EP1032552B1 (de) | 2003-08-06 |
| WO1999025673A1 (de) | 1999-05-27 |
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