NO312201B1 - Fremgangsmåte til fremstilling av konjugert linolsyre - Google Patents
Fremgangsmåte til fremstilling av konjugert linolsyre Download PDFInfo
- Publication number
- NO312201B1 NO312201B1 NO19974882A NO974882A NO312201B1 NO 312201 B1 NO312201 B1 NO 312201B1 NO 19974882 A NO19974882 A NO 19974882A NO 974882 A NO974882 A NO 974882A NO 312201 B1 NO312201 B1 NO 312201B1
- Authority
- NO
- Norway
- Prior art keywords
- linoleic acid
- oil
- alkali
- conjugated linoleic
- conjugated
- Prior art date
Links
- OYHQOLUKZRVURQ-IXWMQOLASA-N linoleic acid Natural products CCCCC\C=C/C\C=C\CCCCCCCC(O)=O OYHQOLUKZRVURQ-IXWMQOLASA-N 0.000 title claims description 37
- 238000000034 method Methods 0.000 title claims description 23
- JBYXPOFIGCOSSB-GOJKSUSPSA-N 9-cis,11-trans-octadecadienoic acid Chemical compound CCCCCC\C=C\C=C/CCCCCCCC(O)=O JBYXPOFIGCOSSB-GOJKSUSPSA-N 0.000 title claims description 21
- 229940108924 conjugated linoleic acid Drugs 0.000 title claims description 21
- 238000002360 preparation method Methods 0.000 title description 2
- DNIAPMSPPWPWGF-UHFFFAOYSA-N propylene glycol Substances CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 claims description 27
- 239000003921 oil Substances 0.000 claims description 18
- 235000019198 oils Nutrition 0.000 claims description 18
- OYHQOLUKZRVURQ-HZJYTTRNSA-N Linoleic acid Chemical compound CCCCC\C=C/C\C=C/CCCCCCCC(O)=O OYHQOLUKZRVURQ-HZJYTTRNSA-N 0.000 claims description 16
- 235000020778 linoleic acid Nutrition 0.000 claims description 16
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 claims description 15
- 239000003513 alkali Substances 0.000 claims description 14
- 235000019197 fats Nutrition 0.000 claims description 14
- 238000006243 chemical reaction Methods 0.000 claims description 12
- 238000006317 isomerization reaction Methods 0.000 claims description 10
- WQDUMFSSJAZKTM-UHFFFAOYSA-N Sodium methoxide Chemical compound [Na+].[O-]C WQDUMFSSJAZKTM-UHFFFAOYSA-N 0.000 claims description 8
- 235000019485 Safflower oil Nutrition 0.000 claims description 6
- 238000004519 manufacturing process Methods 0.000 claims description 6
- 239000003813 safflower oil Substances 0.000 claims description 6
- 235000005713 safflower oil Nutrition 0.000 claims description 6
- 235000019486 Sunflower oil Nutrition 0.000 claims description 3
- 239000002600 sunflower oil Substances 0.000 claims description 3
- 235000005687 corn oil Nutrition 0.000 claims description 2
- 239000002285 corn oil Substances 0.000 claims description 2
- 235000012343 cottonseed oil Nutrition 0.000 claims description 2
- 239000002385 cottonseed oil Substances 0.000 claims description 2
- 239000000944 linseed oil Substances 0.000 claims description 2
- 235000021388 linseed oil Nutrition 0.000 claims description 2
- 239000003549 soybean oil Substances 0.000 claims description 2
- 235000012424 soybean oil Nutrition 0.000 claims description 2
- 239000010497 wheat germ oil Substances 0.000 claims description 2
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 15
- 239000003925 fat Substances 0.000 description 12
- 239000002904 solvent Substances 0.000 description 12
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 9
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 6
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 5
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 4
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 238000007796 conventional method Methods 0.000 description 3
- 235000014113 dietary fatty acids Nutrition 0.000 description 3
- 239000000194 fatty acid Substances 0.000 description 3
- 229930195729 fatty acid Natural products 0.000 description 3
- 150000004665 fatty acids Chemical class 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 239000001149 (9Z,12Z)-octadeca-9,12-dienoate Substances 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- 238000004458 analytical method Methods 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 150000001993 dienes Chemical class 0.000 description 2
- 239000012153 distilled water Substances 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- BZVCUDFTTWZWPF-UHFFFAOYSA-M potassium;ethane-1,2-diol;hydroxide Chemical compound [OH-].[K+].OCCO BZVCUDFTTWZWPF-UHFFFAOYSA-M 0.000 description 2
- 239000011541 reaction mixture Substances 0.000 description 2
- 238000010561 standard procedure Methods 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 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
- WTTJVINHCBCLGX-UHFFFAOYSA-N (9trans,12cis)-methyl linoleate Natural products CCCCCC=CCC=CCCCCCCCC(=O)OC WTTJVINHCBCLGX-UHFFFAOYSA-N 0.000 description 1
- DVWSXZIHSUZZKJ-UHFFFAOYSA-N 18:3n-3 Natural products CCC=CCC=CCC=CCCCCCCCC(=O)OC DVWSXZIHSUZZKJ-UHFFFAOYSA-N 0.000 description 1
- LNJCGNRKWOHFFV-UHFFFAOYSA-N 3-(2-hydroxyethylsulfanyl)propanenitrile Chemical compound OCCSCCC#N LNJCGNRKWOHFFV-UHFFFAOYSA-N 0.000 description 1
- PKIXXJPMNDDDOS-UHFFFAOYSA-N Methyl linoleate Natural products CCCCC=CCCC=CCCCCCCCC(=O)OC PKIXXJPMNDDDOS-UHFFFAOYSA-N 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 230000021615 conjugation Effects 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 229910001873 dinitrogen Inorganic materials 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 238000004817 gas chromatography Methods 0.000 description 1
- 239000011810 insulating material Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- DVWSXZIHSUZZKJ-YSTUJMKBSA-N methyl linolenate Chemical compound CC\C=C/C\C=C/C\C=C/CCCCCCCC(=O)OC DVWSXZIHSUZZKJ-YSTUJMKBSA-N 0.000 description 1
- 235000015097 nutrients Nutrition 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 238000007363 ring formation reaction Methods 0.000 description 1
- 238000007086 side reaction Methods 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- -1 tert-butyl alkoxide Chemical class 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 230000009466 transformation Effects 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11C—FATTY ACIDS FROM FATS, OILS OR WAXES; CANDLES; FATS, OILS OR FATTY ACIDS BY CHEMICAL MODIFICATION OF FATS, OILS, OR FATTY ACIDS OBTAINED THEREFROM
- C11C3/00—Fats, oils, or fatty acids by chemical modification of fats, oils, or fatty acids obtained therefrom
- C11C3/14—Fats, oils, or fatty acids by chemical modification of fats, oils, or fatty acids obtained therefrom by isomerisation
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
- C07C51/347—Preparation of carboxylic acids or their salts, halides or anhydrides by reactions not involving formation of carboxyl groups
- C07C51/353—Preparation of carboxylic acids or their salts, halides or anhydrides by reactions not involving formation of carboxyl groups by isomerisation; by change of size of the carbon skeleton
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- General Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Wood Science & Technology (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Fats And Perfumes (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP8288094A JP3017108B2 (ja) | 1996-10-30 | 1996-10-30 | 共役リノール酸の製造方法 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| NO974882D0 NO974882D0 (no) | 1997-10-23 |
| NO974882L NO974882L (no) | 1998-05-04 |
| NO312201B1 true NO312201B1 (no) | 2002-04-08 |
Family
ID=17725721
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO19974882A NO312201B1 (no) | 1996-10-30 | 1997-10-23 | Fremgangsmåte til fremstilling av konjugert linolsyre |
Country Status (11)
| Country | Link |
|---|---|
| US (1) | US5986116A (de) |
| EP (1) | EP0839897B1 (de) |
| JP (1) | JP3017108B2 (de) |
| KR (1) | KR100289205B1 (de) |
| AU (1) | AU722105B2 (de) |
| CA (1) | CA2219601C (de) |
| DE (1) | DE69704014T2 (de) |
| ID (1) | ID19188A (de) |
| MY (1) | MY116996A (de) |
| NO (1) | NO312201B1 (de) |
| TW (1) | TW393463B (de) |
Families Citing this family (39)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| ATE194387T1 (de) | 1995-11-14 | 2000-07-15 | Loders Croklaan Bv | Prozess für die präparation von substanzen mit hohem gehalt an isomeren von konjugierte linölsäure |
| CA2246085C (en) * | 1997-09-12 | 2004-04-27 | Krish Bhaggan | Production of materials rich in conjugated isomers of long chain polyunsaturated fatty acid residues |
| US6015833A (en) | 1998-03-17 | 2000-01-18 | Conlinco., Inc. | Conjugated linoleic acid compositions |
| JP2003073269A (ja) * | 1998-03-17 | 2003-03-12 | Conlinco Inc | 共役リノール酸組成物 |
| US7776353B1 (en) | 1998-03-17 | 2010-08-17 | Aker Biomarine Asa | Conjugated linoleic acid compositions |
| US7078051B1 (en) | 1998-08-11 | 2006-07-18 | Natural Asa | Conjugated linoleic acid alkyl esters in feedstuffs and food |
| JP2000516480A (ja) * | 1998-03-17 | 2000-12-12 | コンリンコ，インコーポレイテッド | 共役リノール酸組成物 |
| US6696584B2 (en) | 1998-05-04 | 2004-02-24 | Natural Asa | Isomer enriched conjugated linoleic acid compositions |
| KR100402040B1 (de) | 1998-05-04 | 2003-10-17 | 콘린코 인크. | Zusammensetzungen von konjugierter linolsäure die mit isomeren angereichert sind |
| US7101914B2 (en) * | 1998-05-04 | 2006-09-05 | Natural Asa | Isomer enriched conjugated linoleic acid compositions |
| US6060514A (en) | 1998-05-04 | 2000-05-09 | Conlin Co., Inc. | Isomer enriched conjugated linoleic acid compositions |
| US6214372B1 (en) | 1998-05-04 | 2001-04-10 | Con Lin Co., Inc. | Method of using isomer enriched conjugated linoleic acid compositions |
| ITMI991894A1 (it) * | 1999-09-09 | 2001-03-09 | Carlo Ghisalberti | Acido linoleico coniugato e trigliceride nuovi metodi di sintesi e d'uso |
| US7947737B1 (en) | 1999-09-30 | 2011-05-24 | Aker Biomarine Asa | Method of treating hypertension and reducing serum lipase activity |
| US6822104B2 (en) * | 2000-01-12 | 2004-11-23 | Her Majesty The Queen In Right Of Canada, As Represented By The Minister Of Agriculture | Method for commercial preparation of preferred isomeric forms of ester free conjugated fatty acids with solvents systems containing polyether alcohol solvents |
| CA2404799C (en) | 2000-04-06 | 2007-08-07 | Conlinco, Inc. | Conjugated linoleic acid compositions |
| AU2001255431B2 (en) | 2000-04-18 | 2007-01-04 | Natural As | Conjugated linoleic acid powder |
| US20030149288A1 (en) * | 2000-04-18 | 2003-08-07 | Natural Asa | Conjugated linoleic acid powder |
| US6380409B1 (en) * | 2000-04-24 | 2002-04-30 | Conlin Co., Inc. | Methods for preparing CLA isomers |
| US6927239B1 (en) * | 2000-08-02 | 2005-08-09 | Pharmanutrients | Methods and compositions for the attenuation and/or prevention of stress/catabolic responses |
| CN1665566A (zh) | 2000-09-21 | 2005-09-07 | 营养21公司 | 用铬络合物、共轭脂肪酸和 /或共轭脂肪醇治疗糖尿病、减少身体脂肪、改善胰岛素敏感性、缓解高血糖症和高胆固醇血症的方法和组合物 |
| DE10102050A1 (de) | 2001-01-17 | 2002-07-18 | Basf Ag | Zubereitung zur Verbesserung der Nahrungsverwertung |
| US6479683B1 (en) | 2001-03-06 | 2002-11-12 | Ag Processing Inc | Process for conjugating fatty acid esters |
| CA2442106A1 (en) | 2001-03-29 | 2002-10-10 | Basf Aktiengesellschaft | Conjugated unsaturated glyceride mixtures and a method for producing the same |
| US6838971B2 (en) * | 2001-05-21 | 2005-01-04 | Matsushita Electric Industrial Co., Ltd. | Thermal fuse |
| US6677470B2 (en) | 2001-11-20 | 2004-01-13 | Natural Asa | Functional acylglycerides |
| US6414171B1 (en) * | 2001-11-27 | 2002-07-02 | Her Majesty In Right Of Canada, As Represented By The Minister Of Agriculture & Agri-Food Canada | Method for commercial preparation of conjugated linoleic acid from by-products of vegetable oil refining |
| US6409649B1 (en) * | 2001-11-27 | 2002-06-25 | Her Majesty The Queen In Right Of Canada, As Represented By The Minister Of Agriculture & Agri-Food Canada | Method for commercial preparation of conjugated linoleic acid using recycled alkali transesterification catalyst |
| US6743931B2 (en) | 2002-09-24 | 2004-06-01 | Natural Asa | Conjugated linoleic acid compositions |
| US7193096B2 (en) | 2003-07-01 | 2007-03-20 | Loders Croklaan Usa Llc | Process for producing a conjugated di- or poly-unsaturated fatty acid of 12 to 24 carbon atoms or salt or ester thereof |
| CA2436650A1 (en) * | 2003-08-06 | 2005-02-06 | Naturia Inc. | Conjugated linolenic acid (clnatm) compositions: synthesis, purification and uses |
| US20050069593A1 (en) * | 2003-09-29 | 2005-03-31 | Life Time Fitness, Inc. | Nutritional supplement containing 7-Keto-DHEA and conjugated linoleic acid |
| DE10349455A1 (de) * | 2003-10-23 | 2005-05-25 | Bioghurt Biogarde Gmbh & Co. Kg | Verfahren zur Herstellung konjugierter, mehrfach ungesättigter Fettsäureester |
| US7666447B2 (en) * | 2004-10-08 | 2010-02-23 | Pharmanutrients | Compositions including Krill extracts and conjugated linoleic acid and methods of using same |
| US20070049763A1 (en) * | 2005-08-23 | 2007-03-01 | Reaney Martin J | Methods for preparation and use of strong base catalysts |
| CN100369881C (zh) * | 2006-01-13 | 2008-02-20 | 国家海洋局第一海洋研究所 | 高含量9,11共轭亚油酸的组合物及其制备方法 |
| WO2011057731A1 (en) * | 2009-11-10 | 2011-05-19 | Cognis Ip Management Gmbh | A composition comprising a lipid suitable for human consumption |
| CN102229527B (zh) | 2009-12-14 | 2016-05-04 | 脂质营养品有限公司 | 工艺方法 |
| CN104725216A (zh) * | 2015-02-12 | 2015-06-24 | 湖北华龙生物制药有限公司 | 一种从乌桕梓油中纯化分离高纯度α-亚麻酸、亚油酸的方法 |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3984444A (en) * | 1971-11-10 | 1976-10-05 | Hoechst Aktiengesellschaft | Isomerization process of a higher fatty acid ester having isolated double bonds |
| US4164505A (en) * | 1977-07-08 | 1979-08-14 | Sylvachem Corporation | Flow process for conjugating unconjugated unsaturation of fatty acids |
| JPS5495502A (en) * | 1978-01-10 | 1979-07-28 | Japan Synthetic Rubber Co Ltd | Preparation of 3-methyl-2-buten-1-ol |
| US5208356A (en) * | 1989-02-17 | 1993-05-04 | Wisconsin Alumni Research Foundation | Octadecadienoic phospholipic esters, antioxidant and mold inhibiting compositions |
| US5208358A (en) * | 1992-07-13 | 1993-05-04 | Dow Corning Corporation | Process for preparation of silyl ketene acetals |
| US5814663A (en) | 1994-08-29 | 1998-09-29 | Wisconsin Alumni Research Foundation | Method for maintaining an existing level of body fat |
| ES2161969T3 (es) * | 1995-11-14 | 2001-12-16 | Unilever Nv | Grasa comestible para untar. |
| DE19546028C2 (de) * | 1995-12-09 | 2000-04-27 | Fresenius Ag | Bilanzierdisposable zum Bilanzieren von Flüssigkeiten für eine medizinische Behandlungsvorrichtung sowie eine medizinische Behandlungsvorrichtung mit einem Systemeinschub zur Aufnahme eines derartigen Bilanzierdisposables |
-
1996
- 1996-10-30 JP JP8288094A patent/JP3017108B2/ja not_active Expired - Lifetime
-
1997
- 1997-10-23 AU AU42784/97A patent/AU722105B2/en not_active Expired
- 1997-10-23 NO NO19974882A patent/NO312201B1/no not_active IP Right Cessation
- 1997-10-23 EP EP97118467A patent/EP0839897B1/de not_active Revoked
- 1997-10-23 DE DE69704014T patent/DE69704014T2/de not_active Revoked
- 1997-10-24 US US08/957,774 patent/US5986116A/en not_active Expired - Lifetime
- 1997-10-24 MY MYPI97005010A patent/MY116996A/en unknown
- 1997-10-27 TW TW086115866A patent/TW393463B/zh not_active IP Right Cessation
- 1997-10-29 KR KR1019970055819A patent/KR100289205B1/ko not_active Expired - Lifetime
- 1997-10-29 CA CA002219601A patent/CA2219601C/en not_active Expired - Lifetime
- 1997-10-30 ID IDP973555A patent/ID19188A/id unknown
Also Published As
| Publication number | Publication date |
|---|---|
| JP3017108B2 (ja) | 2000-03-06 |
| MY116996A (en) | 2004-04-30 |
| JPH10130199A (ja) | 1998-05-19 |
| AU4278497A (en) | 1998-05-07 |
| NO974882D0 (no) | 1997-10-23 |
| EP0839897A1 (de) | 1998-05-06 |
| CA2219601A1 (en) | 1998-04-30 |
| EP0839897B1 (de) | 2001-01-31 |
| TW393463B (en) | 2000-06-11 |
| AU722105B2 (en) | 2000-07-20 |
| CA2219601C (en) | 2002-03-19 |
| KR19980033256A (ko) | 1998-07-25 |
| NO974882L (no) | 1998-05-04 |
| KR100289205B1 (ko) | 2001-05-02 |
| DE69704014T2 (de) | 2001-06-21 |
| ID19188A (id) | 1998-06-28 |
| US5986116A (en) | 1999-11-16 |
| DE69704014D1 (de) | 2001-03-08 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| MK1K | Patent expired |