CA2219601C - Method for producing conjugated linoleic acid - Google Patents
Method for producing conjugated linoleic acid Download PDFInfo
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- CA2219601C CA2219601C CA002219601A CA2219601A CA2219601C CA 2219601 C CA2219601 C CA 2219601C CA 002219601 A CA002219601 A CA 002219601A CA 2219601 A CA2219601 A CA 2219601A CA 2219601 C CA2219601 C CA 2219601C
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- Prior art keywords
- oil
- linoleic acid
- alkali
- fat
- propylene glycol
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- Expired - Lifetime
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Classifications
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- 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
Abstract
There is provided a method for producing conjugated linoleic acid, comprising subjecting a fat or oil containing linoleic acid to alkali isomerization reaction in an alkali-propylene glycol solution.
Description
METHOD FOR PRODUCING CONJUGATED LINOLEIC ACID
BACKGROUND OF THE INVENTION
Field of the Invention This invention relates to a method for producing conjugated linoleic acid. More particularly, this inven-tion relates to a method for efficiently transforming the linoleic acid contained in a fat or oil into conjugated linoleic acid by carrying out the alkali isomerization of the linoleic acid in a specific solvent.
Background Art As a method for producing conjugated fatty acids, the so-called "alkali isomerization" method is known, in which an organic solvent, typically ethylene glycol, is employed (J. Am. Oil Chem. Soc., 36, 631 (1959); The 34th Annual Meeting on Oil Chemists' Society, p. 171 (1995); and "Standard Methods for the Analysis of~ Fats, Oils and Related Materials", 2.4.16-17). It is reported in the J.
Am. Oil Chem. Soc., 36, 631 (1959) that, when methyl linolenate was heated in a potassium hydroxide-ethylene glycol solution at 200~C for 7 hours, about 80% conversion (conjugation) was attained. However, the reported method also involves cyclization and other side reactions.
According to the 34th Annual Meeting on Oil Chemist's Society, p. 171 (1995), tests were carried out in accor-dance with the method described in the "Standard Methods for the Analysis of Fats, Oils and Related Materials", 2.4.16-17, and the following are reported: when methyl linolate was allowed to react in a potassium hydroxide-ethylene glycol solution at 180~C for 2 hours, the rate of the conjugated diene formed reached approxi-mately 80% or more, and the amount of potassium hydroxide used in this reaction was six times the number of moles of 1,4-butadiene structure; and, when a safflower oil was subjected to isomerization reaction at 30~C for 1.5 hours by using, as solvents, dimethyl sulfoxide and dimethyl-formamide, and, as an alkali, sodium methoxide (in an amount of two times the number of moles of 1,4-butadiene structure), the rate of the conjugated diene formed reached approximately 73%.
Among the three types of solvents reported in the above reference, ethylene glycol is most preferred from the viewpoint of alkali solubility (in the case of the other two solvents, the type of alkalis which can be used is limited, and, the solvents must be used in a large amount).
As discussed above, in the conventional alkali isomeri-zation methods for producing conjugated fatty acids, ethylene glycol, dimethyl sulfoxide or dimethylformamide is used as a solvent. However, these three compounds all have some toxicity. The conventional methods thus have the drawback that the resulting conjugated products cannot be used for foods.
It is therefore an object of the present invention to provide a method for producing conjugated linoleic acid, which can more efficiently transform linoleic acid into conjugated linoleic acid and which makes it possible to use the conjugated product in the field of foods.
SUMMARY OF THE INVENTION
It has now been found by the present inventors that the above object can be attained by using propylene glycol as a solvent in the production of conjugated linoleic acid by the alkali isomerization method.
Thus, the method for producing conjugated linoleic acid according to the present invention comprises subjecting a fat or oil containing linoleic acid to alkali isomerization reaction in an alkali-propylene glycol solution.
The method of the present invention, which utilizes propylene glycol as a solvent, can produce conjugated linoleic acid in a higher yield as compared with the conventional method which uses ethylene glycol, the most preferred solvent conventionally known. In addition, the method of the present invention has the further advantage that the resulting fat or oil containing the conjugated linoleic acid is less colored. Moreover, since propylene glycol is not toxic, the product according to the present invention can be used for foods.
BRIEF DESCRIPTION OF THE DRAWING
Fig. 1 is a graph showing the rate of conversion of linoleic acid into conjugated linoleic acid with respect to the products obtained in Examples and Comparative Examples.
DETAILED DESCRIPTION OF THE INVENTION
According to the method of the present invention, a fat or oil containing linoleic acid is subjected to alkali isomerization reaction carried out in an alkali-propylene glycol solution, whereby the linoleic acid contained in the fat or oil is converted or transformed into conjugated linoleic acid. As the fat or oil containing linoleic acid, any fat or oil such as safflower oil, sunflower oil, corn oil, soybean oil, cottonseed oil, linseed oil or wheat germ oil can be used as long as it contains linoleic acid. Of these, safflower oil and sunflower oil, both having high linoleic acid contents, are preferred.
Examples of the alkali usable in the present invention include potassium hydroxide, sodium methoxide, sodium hydroxide and t-butyl alkoxide. Of these, potassium hydroxide and sodium methoxide are preferred. The alkali may be used generally in an amount of from 1 to 8 times, preferably from 3 to 6 times the number of moles of the linoleic acid contained in the fat or oil.
In the method of the present invention, the amount of propylene glycol, which is used as a solvent, is generally from 1 to 10 times, preferably from 1.5 to 5 times the weight of the fat or oil containing linoleic acid.
The isomerization reaction for transforming the linoleic acid contained in the fat or oil into conjugated linoleic acid is carried out in a solution of the above-described alkali in propylene glycol under a stream of nitrogen. The reaction temperature is generally from 110 to 180~C, preferably from 130 to 170~C. The reaction time is generally from 1 to 5 hours, preferably from 2 to 3 hours. As shown in Examples which will be described later, conjugated linoleic acid can be produced at a high conversion of 80% or more, when the reaction is carried out under the above-described preferable reaction temperature condition.
According to the method of the present invention using, as a solvent, propylene glycol which is not harmful for the human body, the resulting product can be applied not only to conventional uses such as additives for rubbers and insulating materials for IC, but also to foods such as muscle-enhancing agents and nutrition-replenishing foods, for which the products obtained by the conventional alkali isomerization methods cannot be used.
EXAMPLES
The following examples illustrate the present invention but are not intended to limit it.
Example 1 50 g of potassium hydroxide was dissolved in 150 g of propylene glycol. Nitrogen gas was blown into the solution for 20 minutes, and the temperature of the solution was raised to 110~C. Thereafter, 100 g of a safflower oil was added to the solution, and allowed to react at 110~C for 2.5 hours under a stream of nitrogen (the fatty acid composition of the safflower oil used is shown in Table 1).
After the reaction was completed, the reaction mixture was cooled to room temperature, and made neutral by the addition of hydrochloric acid. The mixture was stirred for 15 minutes. Subsequently, the pH of the reaction mixture was adjusted to 3, to which distilled water was added. The resulting mixture was stirred for 5 minutes, and then subjected to extraction with hexane three times. The hexane solution was washed with a 5~ NaCl solution and with distilled water, followed by dewatering and filtration.
Thereafter, the hexane was distilled off to obtain a product containing conjugated linoleic acid. The conjugat-ed linoleic acid content of the product obtained was measured by gas chromatography, thereby determining the rate of conversion of linoleic acid into conjugated linoleic acid. The conversion determined was 26.5~.
Further, the degree of the coloring of the product was measured by the Gardner method (ASTM D1544). As a result, the product was found to have a Gardner color standard number of 3.
Table 1-Fatty Acid Composition of Safflower Oil (~) Fatty AcidBefore ReactionAfter Reaction Palmitic acid 7.0 7.0 Stearic acid 2.6 2.6 Oleic acid 14.4 14.4 Linoleic acid 76.0 55.9 Conjugated linoleic 0 20.1 acid Examples 2 to 7 The procedure of Example 1 was repeated except that the reaction temperature was changed to 120~C (Example 2), 130~C (Example 3), 140~C (Example 4), 150~C (Example 5), 160~C (Example 6) and 170~C (Example 7), thereby obtaining products containing conjugated linoleic acid.
For the products thus obtained, the rate of conversion of linoleic acid into conjugated linoleic acid and the Gardner color standard number were measured. The results are shown in Tables 2 and 3.
Comparative Examples 1 to 7 The procedures of Examples 1 to 7 were respectively repeated except that the solvent was changed from propylene glycol to ethylene glycol, thereby obtaining products containing conjugated linoleic acid. The results of the above measurements are shown in Tables 2 and 3.
Table 2-Rate of Conversion (%) Reaction Temp.(~C) Propylene Glycol Ethylene Glycol 110 26.5(Ex. 1)1.6(Comp.Ex.1) 120 58.4(Ex. 2)14.1(Comp.Ex.2) 130 78.2(Ex. 3)35.7(Comp.Ex.3) 140 85.7(Ex. 4)52.8(Comp.Ex.4) 150 90.0(Ex. 5)63.9(Comp.Ex.5) 160 97.2(Ex. 6)91.5(Comp.Ex.6) 170 99.1(Ex. 7)99.0(Comp.Ex.7) Table 3-Gardner Color Standard Number Reaction Temp.(~C) Propylene Glycol Ethylene Glycol 110 3(Ex. 1)9(Comp. Ex. 1) 120 3(Ex. 2)9(Comp. Ex. 2) 130 3(Ex. 3)9(Comp. Ex. 3) 140 3(Ex. 4)8(Comp. Ex. 4) 150 3(Ex. 5)8(Comp. Ex. 5) 160 2(Ex. 6)6(Comp. Ex. 6) 170 2(Ex. 7)5(Comp. Ex. 7) The relationship between the reaction temperatures and the rates of conversion of linoleic acid into conjugated linoleic acid tabulated in Table 2 is graphically shown in Fig. 1. As is apparent from Fig. 1, the method of the present invention, which uses propylene glycol as a solvent, attains considerably higher rates of conversion of linoleic acid into conjugated linoleic acid, as compared with the conventional method using ethylene glycol as a solvent. The difference in the rate of conversion between the two methods is marked when the reaction temperature is 150~C or lower. Further, as may be appreciated from Table 3, the products containing conjugated linoleic acid obtained by the method of the present invention are much less colored, compared to the products obtained by the conventional process (Gardner color standard number 2:
light yellow - Gardner color standard number 9: brown).
BACKGROUND OF THE INVENTION
Field of the Invention This invention relates to a method for producing conjugated linoleic acid. More particularly, this inven-tion relates to a method for efficiently transforming the linoleic acid contained in a fat or oil into conjugated linoleic acid by carrying out the alkali isomerization of the linoleic acid in a specific solvent.
Background Art As a method for producing conjugated fatty acids, the so-called "alkali isomerization" method is known, in which an organic solvent, typically ethylene glycol, is employed (J. Am. Oil Chem. Soc., 36, 631 (1959); The 34th Annual Meeting on Oil Chemists' Society, p. 171 (1995); and "Standard Methods for the Analysis of~ Fats, Oils and Related Materials", 2.4.16-17). It is reported in the J.
Am. Oil Chem. Soc., 36, 631 (1959) that, when methyl linolenate was heated in a potassium hydroxide-ethylene glycol solution at 200~C for 7 hours, about 80% conversion (conjugation) was attained. However, the reported method also involves cyclization and other side reactions.
According to the 34th Annual Meeting on Oil Chemist's Society, p. 171 (1995), tests were carried out in accor-dance with the method described in the "Standard Methods for the Analysis of Fats, Oils and Related Materials", 2.4.16-17, and the following are reported: when methyl linolate was allowed to react in a potassium hydroxide-ethylene glycol solution at 180~C for 2 hours, the rate of the conjugated diene formed reached approxi-mately 80% or more, and the amount of potassium hydroxide used in this reaction was six times the number of moles of 1,4-butadiene structure; and, when a safflower oil was subjected to isomerization reaction at 30~C for 1.5 hours by using, as solvents, dimethyl sulfoxide and dimethyl-formamide, and, as an alkali, sodium methoxide (in an amount of two times the number of moles of 1,4-butadiene structure), the rate of the conjugated diene formed reached approximately 73%.
Among the three types of solvents reported in the above reference, ethylene glycol is most preferred from the viewpoint of alkali solubility (in the case of the other two solvents, the type of alkalis which can be used is limited, and, the solvents must be used in a large amount).
As discussed above, in the conventional alkali isomeri-zation methods for producing conjugated fatty acids, ethylene glycol, dimethyl sulfoxide or dimethylformamide is used as a solvent. However, these three compounds all have some toxicity. The conventional methods thus have the drawback that the resulting conjugated products cannot be used for foods.
It is therefore an object of the present invention to provide a method for producing conjugated linoleic acid, which can more efficiently transform linoleic acid into conjugated linoleic acid and which makes it possible to use the conjugated product in the field of foods.
SUMMARY OF THE INVENTION
It has now been found by the present inventors that the above object can be attained by using propylene glycol as a solvent in the production of conjugated linoleic acid by the alkali isomerization method.
Thus, the method for producing conjugated linoleic acid according to the present invention comprises subjecting a fat or oil containing linoleic acid to alkali isomerization reaction in an alkali-propylene glycol solution.
The method of the present invention, which utilizes propylene glycol as a solvent, can produce conjugated linoleic acid in a higher yield as compared with the conventional method which uses ethylene glycol, the most preferred solvent conventionally known. In addition, the method of the present invention has the further advantage that the resulting fat or oil containing the conjugated linoleic acid is less colored. Moreover, since propylene glycol is not toxic, the product according to the present invention can be used for foods.
BRIEF DESCRIPTION OF THE DRAWING
Fig. 1 is a graph showing the rate of conversion of linoleic acid into conjugated linoleic acid with respect to the products obtained in Examples and Comparative Examples.
DETAILED DESCRIPTION OF THE INVENTION
According to the method of the present invention, a fat or oil containing linoleic acid is subjected to alkali isomerization reaction carried out in an alkali-propylene glycol solution, whereby the linoleic acid contained in the fat or oil is converted or transformed into conjugated linoleic acid. As the fat or oil containing linoleic acid, any fat or oil such as safflower oil, sunflower oil, corn oil, soybean oil, cottonseed oil, linseed oil or wheat germ oil can be used as long as it contains linoleic acid. Of these, safflower oil and sunflower oil, both having high linoleic acid contents, are preferred.
Examples of the alkali usable in the present invention include potassium hydroxide, sodium methoxide, sodium hydroxide and t-butyl alkoxide. Of these, potassium hydroxide and sodium methoxide are preferred. The alkali may be used generally in an amount of from 1 to 8 times, preferably from 3 to 6 times the number of moles of the linoleic acid contained in the fat or oil.
In the method of the present invention, the amount of propylene glycol, which is used as a solvent, is generally from 1 to 10 times, preferably from 1.5 to 5 times the weight of the fat or oil containing linoleic acid.
The isomerization reaction for transforming the linoleic acid contained in the fat or oil into conjugated linoleic acid is carried out in a solution of the above-described alkali in propylene glycol under a stream of nitrogen. The reaction temperature is generally from 110 to 180~C, preferably from 130 to 170~C. The reaction time is generally from 1 to 5 hours, preferably from 2 to 3 hours. As shown in Examples which will be described later, conjugated linoleic acid can be produced at a high conversion of 80% or more, when the reaction is carried out under the above-described preferable reaction temperature condition.
According to the method of the present invention using, as a solvent, propylene glycol which is not harmful for the human body, the resulting product can be applied not only to conventional uses such as additives for rubbers and insulating materials for IC, but also to foods such as muscle-enhancing agents and nutrition-replenishing foods, for which the products obtained by the conventional alkali isomerization methods cannot be used.
EXAMPLES
The following examples illustrate the present invention but are not intended to limit it.
Example 1 50 g of potassium hydroxide was dissolved in 150 g of propylene glycol. Nitrogen gas was blown into the solution for 20 minutes, and the temperature of the solution was raised to 110~C. Thereafter, 100 g of a safflower oil was added to the solution, and allowed to react at 110~C for 2.5 hours under a stream of nitrogen (the fatty acid composition of the safflower oil used is shown in Table 1).
After the reaction was completed, the reaction mixture was cooled to room temperature, and made neutral by the addition of hydrochloric acid. The mixture was stirred for 15 minutes. Subsequently, the pH of the reaction mixture was adjusted to 3, to which distilled water was added. The resulting mixture was stirred for 5 minutes, and then subjected to extraction with hexane three times. The hexane solution was washed with a 5~ NaCl solution and with distilled water, followed by dewatering and filtration.
Thereafter, the hexane was distilled off to obtain a product containing conjugated linoleic acid. The conjugat-ed linoleic acid content of the product obtained was measured by gas chromatography, thereby determining the rate of conversion of linoleic acid into conjugated linoleic acid. The conversion determined was 26.5~.
Further, the degree of the coloring of the product was measured by the Gardner method (ASTM D1544). As a result, the product was found to have a Gardner color standard number of 3.
Table 1-Fatty Acid Composition of Safflower Oil (~) Fatty AcidBefore ReactionAfter Reaction Palmitic acid 7.0 7.0 Stearic acid 2.6 2.6 Oleic acid 14.4 14.4 Linoleic acid 76.0 55.9 Conjugated linoleic 0 20.1 acid Examples 2 to 7 The procedure of Example 1 was repeated except that the reaction temperature was changed to 120~C (Example 2), 130~C (Example 3), 140~C (Example 4), 150~C (Example 5), 160~C (Example 6) and 170~C (Example 7), thereby obtaining products containing conjugated linoleic acid.
For the products thus obtained, the rate of conversion of linoleic acid into conjugated linoleic acid and the Gardner color standard number were measured. The results are shown in Tables 2 and 3.
Comparative Examples 1 to 7 The procedures of Examples 1 to 7 were respectively repeated except that the solvent was changed from propylene glycol to ethylene glycol, thereby obtaining products containing conjugated linoleic acid. The results of the above measurements are shown in Tables 2 and 3.
Table 2-Rate of Conversion (%) Reaction Temp.(~C) Propylene Glycol Ethylene Glycol 110 26.5(Ex. 1)1.6(Comp.Ex.1) 120 58.4(Ex. 2)14.1(Comp.Ex.2) 130 78.2(Ex. 3)35.7(Comp.Ex.3) 140 85.7(Ex. 4)52.8(Comp.Ex.4) 150 90.0(Ex. 5)63.9(Comp.Ex.5) 160 97.2(Ex. 6)91.5(Comp.Ex.6) 170 99.1(Ex. 7)99.0(Comp.Ex.7) Table 3-Gardner Color Standard Number Reaction Temp.(~C) Propylene Glycol Ethylene Glycol 110 3(Ex. 1)9(Comp. Ex. 1) 120 3(Ex. 2)9(Comp. Ex. 2) 130 3(Ex. 3)9(Comp. Ex. 3) 140 3(Ex. 4)8(Comp. Ex. 4) 150 3(Ex. 5)8(Comp. Ex. 5) 160 2(Ex. 6)6(Comp. Ex. 6) 170 2(Ex. 7)5(Comp. Ex. 7) The relationship between the reaction temperatures and the rates of conversion of linoleic acid into conjugated linoleic acid tabulated in Table 2 is graphically shown in Fig. 1. As is apparent from Fig. 1, the method of the present invention, which uses propylene glycol as a solvent, attains considerably higher rates of conversion of linoleic acid into conjugated linoleic acid, as compared with the conventional method using ethylene glycol as a solvent. The difference in the rate of conversion between the two methods is marked when the reaction temperature is 150~C or lower. Further, as may be appreciated from Table 3, the products containing conjugated linoleic acid obtained by the method of the present invention are much less colored, compared to the products obtained by the conventional process (Gardner color standard number 2:
light yellow - Gardner color standard number 9: brown).
Claims (5)
1. A method for producing conjugated linoleic acid, comprising subjecting a fat or oil containing linoleic acid to alkali isomerization reaction in an alkali-propylene glycol solution.
2. The method according to claim 1, wherein the fat or oil containing linoleic acid is selected from the group consisting of safflower oil, sunflower oil, corn oil, soybean oil, cottonseed oil, linseed oil and wheat germ oil.
3. The method according to claim 1 or 2, wherein the alkali is potassium hydroxide or sodium methoxide.
4. The method according to any of claims 1 to 3, wherein the reaction is carried out at a temperature of 130 to 170ÀC.
5. A method which comprises:
subjecting a fat or oil selected from the group consisting of safflower oil, sunflower oil, corn oil, soybean oil, cottonseed oil, linseed oil and wheat germ oil to alkali isomerization reaction in an alkali-propylene glycol solution using potassium hydroxide or sodium hydroxide in an amount of 1 to 8 moles per mole of linoleic acid contained in the fat or oil and propylene glycol in an amount of 1 to 10 times the weight of the fat or oil at a temperature of 110 to 180ÀC for 1 to 5 hours;
and neutralizing the alkali contained in the so-subjected fat or oil by adding hydrochloric acid.
subjecting a fat or oil selected from the group consisting of safflower oil, sunflower oil, corn oil, soybean oil, cottonseed oil, linseed oil and wheat germ oil to alkali isomerization reaction in an alkali-propylene glycol solution using potassium hydroxide or sodium hydroxide in an amount of 1 to 8 moles per mole of linoleic acid contained in the fat or oil and propylene glycol in an amount of 1 to 10 times the weight of the fat or oil at a temperature of 110 to 180ÀC for 1 to 5 hours;
and neutralizing the alkali contained in the so-subjected fat or oil by adding hydrochloric acid.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP8288094A JP3017108B2 (en) | 1996-10-30 | 1996-10-30 | Method for producing conjugated linoleic acid |
| JP288094/1996 | 1996-10-30 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CA2219601A1 CA2219601A1 (en) | 1998-04-30 |
| CA2219601C true CA2219601C (en) | 2002-03-19 |
Family
ID=17725721
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA002219601A Expired - Lifetime CA2219601C (en) | 1996-10-30 | 1997-10-29 | Method for producing conjugated linoleic acid |
Country Status (11)
| Country | Link |
|---|---|
| US (1) | US5986116A (en) |
| EP (1) | EP0839897B1 (en) |
| JP (1) | JP3017108B2 (en) |
| KR (1) | KR100289205B1 (en) |
| AU (1) | AU722105B2 (en) |
| CA (1) | CA2219601C (en) |
| DE (1) | DE69704014T2 (en) |
| ID (1) | ID19188A (en) |
| MY (1) | MY116996A (en) |
| NO (1) | NO312201B1 (en) |
| TW (1) | TW393463B (en) |
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| AU705157B2 (en) | 1995-11-14 | 1999-05-13 | Loders Croklaan B.V. | Process for the preparation of materials with a high content of long chain polyunsaturated fatty acids |
| CA2246085C (en) | 1997-09-12 | 2004-04-27 | Krish Bhaggan | Production of materials rich in conjugated isomers of long chain polyunsaturated fatty acid residues |
| US7078051B1 (en) | 1998-08-11 | 2006-07-18 | Natural Asa | Conjugated linoleic acid alkyl esters in feedstuffs and food |
| ES2279586T3 (en) | 1998-03-17 | 2007-08-16 | Natural Asa | CONJUGATED LINOLEIC ACID COMPOSITIONS. |
| US7776353B1 (en) | 1998-03-17 | 2010-08-17 | Aker Biomarine Asa | Conjugated linoleic acid compositions |
| JP2003073269A (en) * | 1998-03-17 | 2003-03-12 | Conlinco Inc | Conjugated linoleic acid composition |
| 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 |
| US6214372B1 (en) | 1998-05-04 | 2001-04-10 | Con Lin Co., Inc. | Method of using isomer enriched conjugated linoleic acid compositions |
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| US6696584B2 (en) | 1998-05-04 | 2004-02-24 | Natural Asa | Isomer enriched conjugated linoleic acid compositions |
| ATE366521T1 (en) | 1998-05-04 | 2007-08-15 | Natural Asa | METHOD FOR USE OF CONJUGATED LINOLIC ACID COMPOSITIONS ENRICHED WITH ISOMERS |
| ITMI991894A1 (en) * | 1999-09-09 | 2001-03-09 | Carlo Ghisalberti | CONJUGATED LINOLEIC ACID AND TRIGLYCERIDE NEW METHODS OF SYNTHESIS AND USE |
| 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 |
| AU5144901A (en) | 2000-04-06 | 2001-10-23 | Conlinco Inc | Conjugated linoleic acid compositions |
| US20030149288A1 (en) * | 2000-04-18 | 2003-08-07 | Natural Asa | Conjugated linoleic acid powder |
| EP1274320A2 (en) | 2000-04-18 | 2003-01-15 | Natural AS | 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 |
| ATE271406T1 (en) | 2000-09-21 | 2004-08-15 | Nutrition 21 Inc | CHROME-CONTAINING COMPOSITION FOR TREATING DIABETES, IMPROVING INSULIN SENSITIVITY AND REDUCING HYPERGLYCEMIA, HYPERCHOLESTEROLEMIA AND BODY FAT PERCENTAGE |
| DE10102050A1 (en) | 2001-01-17 | 2002-07-18 | Basf Ag | Food, nutritional supplement, feed or medicament preparations containing conjugated cis/trans-octatrienoic acid, useful e.g. for reducing food intake, improving food utilization or treating cancer or diabetes |
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| AU2002257714B2 (en) | 2001-03-29 | 2007-06-28 | Basf Aktiengesellschaft | Conjugated unsaturated glyceride mixtures and a method for producing the same |
| CN1254836C (en) * | 2001-05-21 | 2006-05-03 | 松下电器产业株式会社 | Fusible thermique |
| 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 |
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| DE10349455A1 (en) * | 2003-10-23 | 2005-05-25 | Bioghurt Biogarde Gmbh & Co. Kg | Process for the preparation of conjugated, polyunsaturated fatty acid esters |
| 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 (en) * | 2006-01-13 | 2008-02-20 | 国家海洋局第一海洋研究所 | High-content 9,11 conjugated linoleic acid composition and preparation method thereof |
| DK2498617T3 (en) * | 2009-11-10 | 2014-09-15 | Cognis Ip Man Gmbh | COMPOSITION CONTAINING A LIPID SUITABLE FOR HUMAN INTAKE |
| CN102229527B (en) | 2009-12-14 | 2016-05-04 | 脂质营养品有限公司 | Process |
| CN104725216A (en) * | 2015-02-12 | 2015-06-24 | 湖北华龙生物制药有限公司 | Method for purifying and separating high-purity alpha-linolenic acid and linoleic acid from Chinese tallow kernel oil |
Family Cites Families (7)
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|---|---|---|---|---|
| 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 |
| DK0779033T3 (en) * | 1995-11-14 | 2001-11-12 | Unilever Nv | Edible grease lubricants |
| DE19546028C2 (en) * | 1995-12-09 | 2000-04-27 | Fresenius Ag | Balancing disposable for balancing liquids for a medical treatment device and a medical treatment device with a system insert for receiving such a balancing disposable |
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1996
- 1996-10-30 JP JP8288094A patent/JP3017108B2/en not_active Expired - Lifetime
-
1997
- 1997-10-23 AU AU42784/97A patent/AU722105B2/en not_active Expired
- 1997-10-23 EP EP97118467A patent/EP0839897B1/en not_active Revoked
- 1997-10-23 NO NO19974882A patent/NO312201B1/en not_active IP Right Cessation
- 1997-10-23 DE DE69704014T patent/DE69704014T2/en 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/en not_active IP Right Cessation
- 1997-10-29 KR KR1019970055819A patent/KR100289205B1/en not_active IP Right Cessation
- 1997-10-29 CA CA002219601A patent/CA2219601C/en not_active Expired - Lifetime
- 1997-10-30 ID IDP973555A patent/ID19188A/en unknown
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| AU722105B2 (en) | 2000-07-20 |
| JPH10130199A (en) | 1998-05-19 |
| EP0839897B1 (en) | 2001-01-31 |
| MY116996A (en) | 2004-04-30 |
| JP3017108B2 (en) | 2000-03-06 |
| EP0839897A1 (en) | 1998-05-06 |
| KR19980033256A (en) | 1998-07-25 |
| TW393463B (en) | 2000-06-11 |
| ID19188A (en) | 1998-06-28 |
| US5986116A (en) | 1999-11-16 |
| DE69704014T2 (en) | 2001-06-21 |
| NO974882D0 (en) | 1997-10-23 |
| NO312201B1 (en) | 2002-04-08 |
| KR100289205B1 (en) | 2001-05-02 |
| CA2219601A1 (en) | 1998-04-30 |
| NO974882L (en) | 1998-05-04 |
| AU4278497A (en) | 1998-05-07 |
| DE69704014D1 (en) | 2001-03-08 |
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