NO312135B1 - Fremstilling av materialer rike på konjugerte isomerer av langkjedede flerumettede fettsyrerestere - Google Patents

Fremstilling av materialer rike på konjugerte isomerer av langkjedede flerumettede fettsyrerestere Download PDF

Info

Publication number: NO312135B1
Authority: NO; Norway
Prior art keywords: oil; polyunsaturated fatty; chain polyunsaturated; solvent; fatty acids
Prior art date: 1997-09-12

Application number

NO19984207A

Other languages

English (en)

Norwegian (no)

Other versions

NO984207L (no

NO984207D0 (no

Inventor

Krish Bhaggan

Frederick William Cain

John Bernhard Harris

Victoria Taran

Original Assignee

Loders Croklaan Bv

Priority date (The priority date 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 date listed.)

1997-09-12

Filing date

1998-09-11

Publication date

2002-03-25

1998-09-11 Application filed by Loders Croklaan Bv filed Critical Loders Croklaan Bv

1998-09-11 Publication of NO984207D0 publication Critical patent/NO984207D0/no

1999-03-15 Publication of NO984207L publication Critical patent/NO984207L/no

2002-03-25 Publication of NO312135B1 publication Critical patent/NO312135B1/no

Links

235000020978 long-chain polyunsaturated fatty acids Nutrition 0.000 title claims abstract description 16
239000000463 material Substances 0.000 title claims abstract description 12
125000005313 fatty acid group Chemical group 0.000 title 1
238000000034 method Methods 0.000 claims abstract description 25
239000002904 solvent Substances 0.000 claims abstract description 20
125000004432 carbon atom Chemical group C* 0.000 claims abstract description 7
125000002887 hydroxy group Chemical group [H]O* 0.000 claims abstract description 6
239000003921 oil Substances 0.000 claims description 20
235000019198 oils Nutrition 0.000 claims description 20
DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 claims description 19
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical group [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims description 15
239000000203 mixture Substances 0.000 claims description 13
239000007858 starting material Substances 0.000 claims description 11
235000021588 free fatty acids Nutrition 0.000 claims description 10
238000006243 chemical reaction Methods 0.000 claims description 8
235000013772 propylene glycol Nutrition 0.000 claims description 8
239000000344 soap Substances 0.000 claims description 8
239000002253 acid Substances 0.000 claims description 6
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 6
125000005907 alkyl ester group Chemical group 0.000 claims description 4
YPFDHNVEDLHUCE-UHFFFAOYSA-N propane-1,3-diol Chemical group OCCCO YPFDHNVEDLHUCE-UHFFFAOYSA-N 0.000 claims description 4
150000007513 acids Chemical class 0.000 claims description 3
238000004519 manufacturing process Methods 0.000 claims description 3
235000019484 Rapeseed oil Nutrition 0.000 claims description 2
235000019485 Safflower oil Nutrition 0.000 claims description 2
235000019486 Sunflower oil Nutrition 0.000 claims description 2
230000002378 acidificating effect Effects 0.000 claims description 2
125000003158 alcohol group Chemical group 0.000 claims description 2
239000000944 linseed oil Substances 0.000 claims description 2
235000021388 linseed oil Nutrition 0.000 claims description 2
235000005713 safflower oil Nutrition 0.000 claims description 2
239000003813 safflower oil Substances 0.000 claims description 2
235000012424 soybean oil Nutrition 0.000 claims description 2
239000002600 sunflower oil Substances 0.000 claims description 2
239000003549 soybean oil Substances 0.000 claims 1
235000013305 food Nutrition 0.000 abstract description 5
239000007795 chemical reaction product Substances 0.000 abstract description 4
238000006317 isomerization reaction Methods 0.000 abstract description 3
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract 1
239000000047 product Substances 0.000 description 23
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 12
QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 10
OYHQOLUKZRVURQ-HZJYTTRNSA-N linoleic acid group Chemical class C(CCCCCCC\C=C/C\C=C/CCCCC)(=O)O OYHQOLUKZRVURQ-HZJYTTRNSA-N 0.000 description 8
235000015655 Crocus sativus Nutrition 0.000 description 6
244000124209 Crocus sativus Species 0.000 description 6
PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 6
239000004248 saffron Substances 0.000 description 6
235000013974 saffron Nutrition 0.000 description 6
239000000243 solution Substances 0.000 description 6
235000020778 linoleic acid Nutrition 0.000 description 5
OYHQOLUKZRVURQ-IXWMQOLASA-N linoleic acid Natural products CCCCC\C=C/C\C=C\CCCCCCCC(O)=O OYHQOLUKZRVURQ-IXWMQOLASA-N 0.000 description 5
238000003756 stirring Methods 0.000 description 5
239000011541 reaction mixture Substances 0.000 description 4
208000016444 Benign adult familial myoclonic epilepsy Diseases 0.000 description 3
239000008346 aqueous phase Substances 0.000 description 3
208000016427 familial adult myoclonic epilepsy Diseases 0.000 description 3
235000019387 fatty acid methyl ester Nutrition 0.000 description 3
ZGNITFSDLCMLGI-UHFFFAOYSA-N flubendiamide Chemical compound CC1=CC(C(F)(C(F)(F)F)C(F)(F)F)=CC=C1NC(=O)C1=CC=CC(I)=C1C(=O)NC(C)(C)CS(C)(=O)=O ZGNITFSDLCMLGI-UHFFFAOYSA-N 0.000 description 3
SYSQUGFVNFXIIT-UHFFFAOYSA-N n-[4-(1,3-benzoxazol-2-yl)phenyl]-4-nitrobenzenesulfonamide Chemical class C1=CC([N+](=O)[O-])=CC=C1S(=O)(=O)NC1=CC=C(C=2OC3=CC=CC=C3N=2)C=C1 SYSQUGFVNFXIIT-UHFFFAOYSA-N 0.000 description 3
JBYXPOFIGCOSSB-UQGDGPGGSA-N rumenic acid Chemical compound CCCCCC\C=C/C=C/CCCCCCCC(O)=O JBYXPOFIGCOSSB-UQGDGPGGSA-N 0.000 description 3
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
DTOSIQBPPRVQHS-PDBXOOCHSA-N alpha-linolenic acid Chemical class CC\C=C/C\C=C/C\C=C/CCCCCCCC(O)=O DTOSIQBPPRVQHS-PDBXOOCHSA-N 0.000 description 2
235000020661 alpha-linolenic acid Nutrition 0.000 description 2
229940108924 conjugated linoleic acid Drugs 0.000 description 2
239000012153 distilled water Substances 0.000 description 2
239000008188 pellet Substances 0.000 description 2
239000011734 sodium Substances 0.000 description 2
239000000126 substance 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
229910000619 316 stainless steel Inorganic materials 0.000 description 1
IBWPUTAKVGZXRB-UHFFFAOYSA-N 4-(1,3-benzodioxol-5-yl)butan-2-ylhydrazine Chemical compound NNC(C)CCC1=CC=C2OCOC2=C1 IBWPUTAKVGZXRB-UHFFFAOYSA-N 0.000 description 1
JBYXPOFIGCOSSB-GOJKSUSPSA-N 9-cis,11-trans-octadecadienoic acid Chemical class CCCCCC\C=C\C=C/CCCCCCCC(O)=O JBYXPOFIGCOSSB-GOJKSUSPSA-N 0.000 description 1
239000007864 aqueous solution Substances 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
230000000052 comparative effect Effects 0.000 description 1
238000005485 electric heating Methods 0.000 description 1
230000002255 enzymatic effect Effects 0.000 description 1
235000012041 food component Nutrition 0.000 description 1
239000005417 food ingredient Substances 0.000 description 1
229960004488 linolenic acid Drugs 0.000 description 1
KQQKGWQCNNTQJW-UHFFFAOYSA-N linolenic acid Natural products CC=CCCC=CCC=CCCCCCCCC(O)=O KQQKGWQCNNTQJW-UHFFFAOYSA-N 0.000 description 1
125000005481 linolenic acid group Chemical group 0.000 description 1
150000004668 long chain fatty acids Chemical class 0.000 description 1
229910052757 nitrogen Inorganic materials 0.000 description 1
239000003960 organic solvent Substances 0.000 description 1
235000020777 polyunsaturated fatty acids Nutrition 0.000 description 1
239000008149 soap solution Substances 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
- C12P7/00—Preparation of oxygen-containing organic compounds
- C12P7/64—Fats; Fatty oils; Ester-type waxes; Higher fatty acids, i.e. having at least seven carbon atoms in an unbroken chain bound to a carboxyl group; Oxidised oils or fats
- C12P7/6409—Fatty acids
- C12P7/6427—Polyunsaturated fatty acids [PUFA], i.e. having two or more double bonds in their backbone
- C12P7/6431—Linoleic acids [18:2[n-6]]
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23D—EDIBLE OILS OR FATS, e.g. MARGARINES, SHORTENINGS OR COOKING OILS
- A23D9/00—Other edible oils or fats, e.g. shortenings or cooking oils
- 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
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
- C12P7/00—Preparation of oxygen-containing organic compounds
- C12P7/64—Fats; Fatty oils; Ester-type waxes; Higher fatty acids, i.e. having at least seven carbon atoms in an unbroken chain bound to a carboxyl group; Oxidised oils or fats
- C12P7/6436—Fatty acid esters
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
- C12P7/00—Preparation of oxygen-containing organic compounds
- C12P7/64—Fats; Fatty oils; Ester-type waxes; Higher fatty acids, i.e. having at least seven carbon atoms in an unbroken chain bound to a carboxyl group; Oxidised oils or fats
- C12P7/6436—Fatty acid esters
- C12P7/6445—Glycerides
- C12P7/6472—Glycerides containing polyunsaturated fatty acid [PUFA] residues, i.e. having two or more double bonds in their backbone

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Life Sciences & Earth Sciences (AREA)
Engineering & Computer Science (AREA)
Wood Science & Technology (AREA)
Zoology (AREA)
Oil, Petroleum & Natural Gas (AREA)
General Chemical & Material Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Bioinformatics & Cheminformatics (AREA)
General Engineering & Computer Science (AREA)
Microbiology (AREA)
Genetics & Genomics (AREA)
Health & Medical Sciences (AREA)
Biochemistry (AREA)
General Health & Medical Sciences (AREA)
Biotechnology (AREA)
Food Science & Technology (AREA)
Polymers & Plastics (AREA)
Fats And Perfumes (AREA)
Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Edible Oils And Fats (AREA)

NO19984207A 1997-09-12 1998-09-11 Fremstilling av materialer rike på konjugerte isomerer av langkjedede flerumettede fettsyrerestere NO312135B1 (no)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
EP97307110		1997-09-12

Publications (3)

Publication Number	Publication Date
NO984207D0 NO984207D0 (no)	1998-09-11
NO984207L NO984207L (no)	1999-03-15
NO312135B1 true NO312135B1 (no)	2002-03-25

Family

ID=8229510

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NO19984207A NO312135B1 (no)	1997-09-12	1998-09-11	Fremstilling av materialer rike på konjugerte isomerer av langkjedede flerumettede fettsyrerestere

Country Status (10)

Country	Link
US (2)	US6160140A (de)
EP (1)	EP0902082B1 (de)
AT (1)	ATE245688T1 (de)
AU (1)	AU727994B2 (de)
CA (1)	CA2246085C (de)
DE (1)	DE69816545T2 (de)
DK (1)	DK0902082T3 (de)
ES (1)	ES2206828T3 (de)
NO (1)	NO312135B1 (de)
ZA (1)	ZA987962B (de)

Families Citing this family (31)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
EP1100489B2 (de) †	1997-06-23	2010-08-04	Cornell Research Foundation, Inc.	Methode zur änderung der nährmittelzusammenstellung der milch die durch milchspendende tiere abgesonderd wird
US7078051B1 (en)	1998-08-11	2006-07-18	Natural Asa	Conjugated linoleic acid alkyl esters in feedstuffs and food
US6015833A (en)	1998-03-17	2000-01-18	Conlinco., Inc.	Conjugated linoleic acid compositions
US7776353B1 (en)	1998-03-17	2010-08-17	Aker Biomarine Asa	Conjugated linoleic acid compositions
CA2289648C (en)	1998-03-17	2004-06-01	Conlinco, Inc.	Conjugated linoleic acid compositions
US7101914B2 (en) *	1998-05-04	2006-09-05	Natural Asa	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
JP2000144170A (ja) *	1998-09-01	2000-05-26	Janifu Tekku:Kk	抗肥満及び内臓蓄積脂肪低減化機能を有する物質、及びその用途
CA2404799C (en)	2000-04-06	2007-08-07	Conlinco, Inc.	Conjugated linoleic acid compositions
CA2405819C (en)	2000-04-18	2010-02-09	Duane Fimreite	Conjugated linoleic acid powder
US20030149288A1 (en) *	2000-04-18	2003-08-07	Natural Asa	Conjugated linoleic acid powder
DE10046402B4 (de)	2000-09-18	2006-04-20	Cognis Ip Management Gmbh	Verfahren zur Herstellung von Rohstoffen für die Gewinnung von konjugierter Linolsäure
US6677470B2 (en)	2001-11-20	2004-01-13	Natural Asa	Functional acylglycerides
US6743931B2 (en)	2002-09-24	2004-06-01	Natural Asa	Conjugated linoleic acid compositions
US6897327B2 (en) *	2003-05-08	2005-05-24	Stepan Company	Manufacture of conjugated linoleic salts and acids
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
US20070191619A1 (en) *	2003-12-23	2007-08-16	Stepan Company	Production and purification of esters of conjugated linoleic acids
HU227137B1 (en) *	2003-12-30	2010-08-30	Bunge Noevenyolajipari Zartkoe	Process for producing conjugated linoleic acid
EP1729851A2 (de)	2004-03-10	2006-12-13	Natural ASA	Zusammensetzungen mit reversen isomeren konjugierter linolensäure
CA2513340A1 (en) *	2004-08-25	2006-02-25	F. Hoffmann-La Roche Ag	Reusable substrate for dna microarray production
DE102004043824A1 (de) *	2004-09-10	2006-03-16	Cognis Ip Management Gmbh	Emulsionen mit ungesättigten Fettsäuren und deren Estern
US7910757B2 (en)	2005-02-04	2011-03-22	Lipid Nutrition B.V.	Process for the preparation of fatty acids
WO2007070302A2 (en) *	2005-12-05	2007-06-21	Stepan Company	Process for preparing conjugated linoleic acid and derivatives thereof from ricinoleic acid
WO2007118614A1 (en)	2006-04-13	2007-10-25	Lipid Nutrition B.V.	Process for producing isomer enriched conjugated linoleic acid compositions
US8038853B2 (en) *	2007-06-18	2011-10-18	E.I. Du Pont De Nemours And Company	Photo-induced reduction-oxidation chemistry of carbon nanotubes
EP2055199B1 (de)	2007-10-29	2013-07-31	Stepan Specialty Products, LLC	Verbandzusammensetzung
CN102229527B (zh) *	2009-12-14	2016-05-04	脂质营养品有限公司	工艺方法
EP2366766B8 (de)	2010-03-09	2017-04-19	Stepan Specialty Products, LLC	Verfahren zur Behandlung von Speiseöl, und so erhaltenes Speiseöl
CN102559389A (zh)	2010-12-31	2012-07-11	脂质营养品有限公司	共轭亚油酸的制备方法
CN103748200B (zh) *	2011-08-24	2015-07-01	J-制油株式会社	氧化且部分氢化的油脂

Family Cites Families (9)

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Publication number	Priority date	Publication date	Assignee	Title
US2242230A (en) *		1941-05-20		Process of producing conjugation in
US2343644A (en) *	1941-07-30	1944-03-07	Distillation Products Inc	Procedure for the preparation of substances containing conjugated double bonds
US5208356A (en) *	1989-02-17	1993-05-04	Wisconsin Alumni Research Foundation	Octadecadienoic phospholipic esters, antioxidant and mold inhibiting compositions
US5760082C1 (en) *	1994-08-29	2001-03-06	Wisconsin Alumni Res Found	Dietetic foods containing conjugated linoleic acids
US5814663A (en) *	1994-08-29	1998-09-29	Wisconsin Alumni Research Foundation	Method for maintaining an existing level of body fat
EP0779033B1 (de) *	1995-11-14	2001-09-26	Unilever N.V.	Essbarer Brotaufstrich
JP3017108B2 (ja) *	1996-10-30	2000-03-06	リノール油脂株式会社	共役リノール酸の製造方法
US6015833A (en)	1998-03-17	2000-01-18	Conlinco., Inc.	Conjugated linoleic acid compositions
US6060514A (en)	1998-05-04	2000-05-09	Conlin Co., Inc.	Isomer enriched conjugated linoleic acid compositions

1998
- 1998-08-28 CA CA002246085A patent/CA2246085C/en not_active Expired - Fee Related
- 1998-08-31 DE DE69816545T patent/DE69816545T2/de not_active Expired - Lifetime
- 1998-08-31 AT AT98202886T patent/ATE245688T1/de active
- 1998-08-31 ES ES98202886T patent/ES2206828T3/es not_active Expired - Lifetime
- 1998-08-31 DK DK98202886T patent/DK0902082T3/da active
- 1998-08-31 EP EP98202886A patent/EP0902082B1/de not_active Expired - Lifetime
- 1998-09-01 ZA ZA9807962A patent/ZA987962B/xx unknown
- 1998-09-11 AU AU84160/98A patent/AU727994B2/en not_active Ceased
- 1998-09-11 NO NO19984207A patent/NO312135B1/no not_active IP Right Cessation
- 1998-09-11 US US09/151,776 patent/US6160140A/en not_active Expired - Lifetime
2000
- 2000-07-14 US US09/617,510 patent/US6271404B1/en not_active Expired - Lifetime

Also Published As

Publication number	Publication date
US6160140A (en)	2000-12-12
NO984207L (no)	1999-03-15
DE69816545D1 (de)	2003-08-28
ES2206828T3 (es)	2004-05-16
DK0902082T3 (da)	2003-10-20
DE69816545T2 (de)	2004-06-09
AU8416098A (en)	1999-03-25
ZA987962B (en)	2000-03-01
CA2246085A1 (en)	1999-03-12
EP0902082A1 (de)	1999-03-17
US6271404B1 (en)	2001-08-07
CA2246085C (en)	2004-04-27
NO984207D0 (no)	1998-09-11
ATE245688T1 (de)	2003-08-15
EP0902082B1 (de)	2003-07-23
AU727994B2 (en)	2001-01-04

Legal Events

Date	Code	Title	Description
2018-10-08	MK1K	Patent expired

Publication	Publication Date	Title
NO312135B1 (no)	2002-03-25	Fremstilling av materialer rike på konjugerte isomerer av langkjedede flerumettede fettsyrerestere
US3753968A (en)	1973-08-21	Selective reaction of fatty acids and their separation
AU2021201921B2 (en)	2022-08-04	Polyunsaturated fatty acid triglyceride and preparation and uses thereof
JPH08113549A (ja)	1996-05-07	重合プロセス
EP1844131B1 (de)	2011-05-11	Verfahren zur herstellung von fettsäuren
JP2004041187A (ja)	2004-02-12	長鎖多不飽和脂肪酸の含有量が高い材料の調製方法
EP0069405B1 (de)	1984-10-10	Verfahren zum Trimerisieren ungesättigter Fettsäuren
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