AU596411B2 - Edible fats - Google Patents
Edible fats Download PDFInfo
- Publication number
- AU596411B2 AU596411B2 AU72481/87A AU7248187A AU596411B2 AU 596411 B2 AU596411 B2 AU 596411B2 AU 72481/87 A AU72481/87 A AU 72481/87A AU 7248187 A AU7248187 A AU 7248187A AU 596411 B2 AU596411 B2 AU 596411B2
- Authority
- AU
- Australia
- Prior art keywords
- process according
- rearrangement
- reaction mixture
- catalyst
- fats
- 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.)
- Ceased
Links
- 239000003925 fat Substances 0.000 title claims description 11
- 239000003054 catalyst Substances 0.000 claims description 23
- 238000000034 method Methods 0.000 claims description 20
- 230000008707 rearrangement Effects 0.000 claims description 18
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 16
- 102000004882 Lipase Human genes 0.000 claims description 15
- 108090001060 Lipase Proteins 0.000 claims description 15
- 150000003626 triacylglycerols Chemical class 0.000 claims description 14
- 125000005456 glyceride group Chemical group 0.000 claims description 12
- 239000000203 mixture Substances 0.000 claims description 12
- 239000000047 product Substances 0.000 claims description 12
- 235000019486 Sunflower oil Nutrition 0.000 claims description 10
- 235000019197 fats Nutrition 0.000 claims description 10
- 239000003921 oil Substances 0.000 claims description 10
- 235000019198 oils Nutrition 0.000 claims description 10
- 239000002600 sunflower oil Substances 0.000 claims description 10
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 claims description 9
- 239000002904 solvent Substances 0.000 claims description 9
- 239000006227 byproduct Substances 0.000 claims description 7
- 150000004671 saturated fatty acids Chemical class 0.000 claims description 7
- 150000004665 fatty acids Chemical class 0.000 claims description 6
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 5
- 230000000694 effects Effects 0.000 claims description 5
- 150000002148 esters Chemical class 0.000 claims description 5
- 239000000194 fatty acid Substances 0.000 claims description 5
- 229930195729 fatty acid Natural products 0.000 claims description 5
- 238000002360 preparation method Methods 0.000 claims description 5
- 239000011541 reaction mixture Substances 0.000 claims description 5
- 235000009508 confectionery Nutrition 0.000 claims description 4
- 235000003441 saturated fatty acids Nutrition 0.000 claims description 4
- 235000014593 oils and fats Nutrition 0.000 claims description 3
- 229940049964 oleate Drugs 0.000 claims description 3
- OYHQOLUKZRVURQ-HZJYTTRNSA-N Linoleic acid Chemical compound CCCCC\C=C/C\C=C/CCCCCCCC(O)=O OYHQOLUKZRVURQ-HZJYTTRNSA-N 0.000 claims description 2
- 238000010924 continuous production Methods 0.000 claims description 2
- 238000001640 fractional crystallisation Methods 0.000 claims description 2
- 235000020778 linoleic acid Nutrition 0.000 claims description 2
- OYHQOLUKZRVURQ-IXWMQOLASA-N linoleic acid Natural products CCCCC\C=C/C\C=C\CCCCCCCC(O)=O OYHQOLUKZRVURQ-IXWMQOLASA-N 0.000 claims description 2
- 239000000376 reactant Substances 0.000 description 13
- CKQVRZJOMJRTOY-UHFFFAOYSA-N octadecanoic acid;propane-1,2,3-triol Chemical compound OCC(O)CO.CCCCCCCCCCCCCCCCCC(O)=O CKQVRZJOMJRTOY-UHFFFAOYSA-N 0.000 description 10
- 239000004367 Lipase Substances 0.000 description 9
- 235000019421 lipase Nutrition 0.000 description 9
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 8
- 235000018936 Vitellaria paradoxa Nutrition 0.000 description 8
- PHYFQTYBJUILEZ-IUPFWZBJSA-N triolein Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OCC(OC(=O)CCCCCCC\C=C/CCCCCCCC)COC(=O)CCCCCCC\C=C/CCCCCCCC PHYFQTYBJUILEZ-IUPFWZBJSA-N 0.000 description 7
- DCXXMTOCNZCJGO-UHFFFAOYSA-N tristearoylglycerol Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(OC(=O)CCCCCCCCCCCCCCCCC)COC(=O)CCCCCCCCCCCCCCCCC DCXXMTOCNZCJGO-UHFFFAOYSA-N 0.000 description 7
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 6
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 6
- 229920006395 saturated elastomer Polymers 0.000 description 6
- 239000002253 acid Substances 0.000 description 5
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical class CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 5
- UFTFJSFQGQCHQW-UHFFFAOYSA-N triformin Chemical compound O=COCC(OC=O)COC=O UFTFJSFQGQCHQW-UHFFFAOYSA-N 0.000 description 5
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- 102000004190 Enzymes Human genes 0.000 description 4
- 108090000790 Enzymes Proteins 0.000 description 4
- 235000021355 Stearic acid Nutrition 0.000 description 4
- 238000006243 chemical reaction Methods 0.000 description 4
- 238000009884 interesterification Methods 0.000 description 4
- 238000002844 melting Methods 0.000 description 4
- FLIACVVOZYBSBS-UHFFFAOYSA-N Methyl hexadecanoate Natural products CCCCCCCCCCCCCCCC(=O)OC FLIACVVOZYBSBS-UHFFFAOYSA-N 0.000 description 3
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 3
- 239000007795 chemical reaction product Substances 0.000 description 3
- ZQPPMHVWECSIRJ-MDZDMXLPSA-N elaidic acid Chemical compound CCCCCCCC\C=C\CCCCCCCC(O)=O ZQPPMHVWECSIRJ-MDZDMXLPSA-N 0.000 description 3
- 238000006317 isomerization reaction Methods 0.000 description 3
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 3
- 239000007791 liquid phase Substances 0.000 description 3
- 230000008018 melting Effects 0.000 description 3
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 3
- IPCSVZSSVZVIGE-UHFFFAOYSA-N palmitic acid group Chemical group C(CCCCCCCCCCCCCCC)(=O)O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 3
- 239000008117 stearic acid Substances 0.000 description 3
- 235000015112 vegetable and seed oil Nutrition 0.000 description 3
- 239000008158 vegetable oil Substances 0.000 description 3
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 2
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 2
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 2
- 241000208818 Helianthus Species 0.000 description 2
- 235000003222 Helianthus annuus Nutrition 0.000 description 2
- TUNFSRHWOTWDNC-UHFFFAOYSA-N Myristic acid Natural products CCCCCCCCCCCCCC(O)=O TUNFSRHWOTWDNC-UHFFFAOYSA-N 0.000 description 2
- 239000005642 Oleic acid Substances 0.000 description 2
- 235000021314 Palmitic acid Nutrition 0.000 description 2
- 241000235403 Rhizomucor miehei Species 0.000 description 2
- WQDUMFSSJAZKTM-UHFFFAOYSA-N Sodium methoxide Chemical compound [Na+].[O-]C WQDUMFSSJAZKTM-UHFFFAOYSA-N 0.000 description 2
- 244000299461 Theobroma cacao Species 0.000 description 2
- 235000014121 butter Nutrition 0.000 description 2
- 235000019219 chocolate Nutrition 0.000 description 2
- 235000019841 confectionery fat Nutrition 0.000 description 2
- 235000012343 cottonseed oil Nutrition 0.000 description 2
- XIRNKXNNONJFQO-UHFFFAOYSA-N ethyl hexadecanoate Chemical compound CCCCCCCCCCCCCCCC(=O)OCC XIRNKXNNONJFQO-UHFFFAOYSA-N 0.000 description 2
- 235000013305 food Nutrition 0.000 description 2
- 235000021588 free fatty acids Nutrition 0.000 description 2
- 230000003647 oxidation Effects 0.000 description 2
- 238000007254 oxidation reaction Methods 0.000 description 2
- 239000003208 petroleum Substances 0.000 description 2
- 238000006462 rearrangement reaction Methods 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
- TWJNQYPJQDRXPH-UHFFFAOYSA-N 2-cyanobenzohydrazide Chemical compound NNC(=O)C1=CC=CC=C1C#N TWJNQYPJQDRXPH-UHFFFAOYSA-N 0.000 description 1
- MTJGVAJYTOXFJH-UHFFFAOYSA-N 3-aminonaphthalene-1,5-disulfonic acid Chemical compound C1=CC=C(S(O)(=O)=O)C2=CC(N)=CC(S(O)(=O)=O)=C21 MTJGVAJYTOXFJH-UHFFFAOYSA-N 0.000 description 1
- 241000228212 Aspergillus Species 0.000 description 1
- 241000228245 Aspergillus niger Species 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- 240000005323 Hoya carnosa Species 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 235000021360 Myristic acid Nutrition 0.000 description 1
- 241000729876 Niveus Species 0.000 description 1
- 241000235527 Rhizopus Species 0.000 description 1
- 240000005384 Rhizopus oryzae Species 0.000 description 1
- ZVQOOHYFBIDMTQ-UHFFFAOYSA-N [methyl(oxido){1-[6-(trifluoromethyl)pyridin-3-yl]ethyl}-lambda(6)-sulfanylidene]cyanamide Chemical compound N#CN=S(C)(=O)C(C)C1=CC=C(C(F)(F)F)N=C1 ZVQOOHYFBIDMTQ-UHFFFAOYSA-N 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 125000005907 alkyl ester group Chemical group 0.000 description 1
- 230000002547 anomalous effect Effects 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 150000001805 chlorine compounds Chemical class 0.000 description 1
- 229940110456 cocoa butter Drugs 0.000 description 1
- 235000019868 cocoa butter Nutrition 0.000 description 1
- 239000013065 commercial product Substances 0.000 description 1
- 239000002385 cottonseed oil Substances 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 239000008157 edible vegetable oil Substances 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 229940067592 ethyl palmitate Drugs 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 239000011552 falling film Substances 0.000 description 1
- 150000002190 fatty acyls Chemical group 0.000 description 1
- SLGWESQGEUXWJQ-UHFFFAOYSA-N formaldehyde;phenol Chemical compound O=C.OC1=CC=CC=C1 SLGWESQGEUXWJQ-UHFFFAOYSA-N 0.000 description 1
- 238000005194 fractionation Methods 0.000 description 1
- IPCSVZSSVZVIGE-UHFFFAOYSA-M hexadecanoate Chemical compound CCCCCCCCCCCCCCCC([O-])=O IPCSVZSSVZVIGE-UHFFFAOYSA-M 0.000 description 1
- 235000021083 high saturated fats Nutrition 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 238000005984 hydrogenation reaction Methods 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 238000005342 ion exchange Methods 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 235000013310 margarine Nutrition 0.000 description 1
- 239000003264 margarine Substances 0.000 description 1
- 150000004702 methyl esters Chemical class 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 239000003471 mutagenic agent Substances 0.000 description 1
- 231100000707 mutagenic chemical Toxicity 0.000 description 1
- 230000003505 mutagenic effect Effects 0.000 description 1
- 229940105132 myristate Drugs 0.000 description 1
- WQEPLUUGTLDZJY-UHFFFAOYSA-N n-Pentadecanoic acid Natural products CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-UHFFFAOYSA-N 0.000 description 1
- 239000012454 non-polar solvent Substances 0.000 description 1
- 239000004006 olive oil Substances 0.000 description 1
- 235000008390 olive oil Nutrition 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229920001568 phenolic resin Polymers 0.000 description 1
- 238000003976 plant breeding Methods 0.000 description 1
- 238000007670 refining Methods 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 230000002441 reversible effect Effects 0.000 description 1
- 101150043652 secs-1 gene Proteins 0.000 description 1
- 238000004904 shortening Methods 0.000 description 1
- 239000000741 silica gel Substances 0.000 description 1
- 229910002027 silica gel Inorganic materials 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 235000020238 sunflower seed Nutrition 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 125000005314 unsaturated fatty acid group Chemical group 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 239000012610 weak anion exchange resin Substances 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
- C11C3/04—Fats, oils, or fatty acids by chemical modification of fats, oils, or fatty acids obtained therefrom by esterification of fats or fatty oils
- C11C3/10—Ester interchange
-
- 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
- C11C3/04—Fats, oils, or fatty acids by chemical modification of fats, oils, or fatty acids obtained therefrom by esterification of fats or fatty oils
- C11C3/08—Fats, oils, or fatty acids by chemical modification of fats, oils, or fatty acids obtained therefrom by esterification of fats or fatty oils with fatty acids
Landscapes
- Chemical & Material Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Edible Oils And Fats (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Fats And Perfumes (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB08610979A GB2190394A (en) | 1986-05-06 | 1986-05-06 | Edible fats by rearrangement of sunflower oil |
| GB8610979 | 1986-05-06 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| AU7248187A AU7248187A (en) | 1987-11-12 |
| AU596411B2 true AU596411B2 (en) | 1990-05-03 |
Family
ID=10597386
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AU72481/87A Ceased AU596411B2 (en) | 1986-05-06 | 1987-05-04 | Edible fats |
Country Status (6)
| Country | Link |
|---|---|
| EP (1) | EP0245076A3 (enrdf_load_stackoverflow) |
| JP (1) | JPS6317697A (enrdf_load_stackoverflow) |
| AU (1) | AU596411B2 (enrdf_load_stackoverflow) |
| GB (1) | GB2190394A (enrdf_load_stackoverflow) |
| SE (1) | SE467860B (enrdf_load_stackoverflow) |
| ZA (1) | ZA873239B (enrdf_load_stackoverflow) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU615969B2 (en) * | 1987-10-13 | 1991-10-17 | Lubrizol Corporation, The | Method of producing cis-9-octadecenoic acid compositions |
Families Citing this family (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2504987B2 (ja) * | 1987-04-03 | 1996-06-05 | 不二製油株式会社 | ハ−ドバタ−組成物 |
| GB8925352D0 (en) * | 1989-11-09 | 1989-12-28 | Unilever Plc | Fats |
| EP0519542A1 (en) * | 1991-06-17 | 1992-12-23 | Unilever N.V. | Combined fractionation, refining and interesterification process |
| EP0652289A1 (en) * | 1993-11-05 | 1995-05-10 | Unilever Plc | Random interesterification of triglyceride fats |
| US6229033B1 (en) | 1998-05-11 | 2001-05-08 | E. I. Du Pont De Nemours And Company | Fat products from high stearic soybean oil and a method for the production thereof |
| EP1040761A1 (en) * | 1999-03-19 | 2000-10-04 | Loders Croklaan B.V. | Fat mixtures |
| US6277433B1 (en) | 1999-03-19 | 2001-08-21 | Loders Croklaan B.V. | Fat mixtures |
| US8202712B2 (en) | 2005-09-08 | 2012-06-19 | Loders Croklaan B.V. | Triglyceride process |
| EP1928989B1 (en) * | 2005-09-08 | 2011-11-09 | Loders Croklaan B.V. | Process for producing triglycerides |
| US20130096331A1 (en) * | 2007-12-20 | 2013-04-18 | Dow Agrosciences Llc | Interesterification of low saturate sunflower oil and related methods and compositions |
| DK2251428T3 (da) | 2009-05-11 | 2012-01-30 | Loders Croklaan Bv | Fremgangsmåde til fremstilling af en triglyceridsammensætning |
| KR101314682B1 (ko) * | 2010-04-22 | 2013-10-07 | 씨제이제일제당 (주) | 카카오 버터 유사 하드버터의 제조 방법 |
| CN101878821A (zh) * | 2010-05-05 | 2010-11-10 | 江南大学 | 可可脂改良剂的生物合成 |
| CN102634547A (zh) * | 2012-03-28 | 2012-08-15 | 江南大学 | 一种对称型甘油三酯的制备方法 |
| SG11201501614PA (en) * | 2012-09-07 | 2015-04-29 | Aak Ab | Process for production of cocoa butter equivalent |
| WO2014097218A1 (pt) * | 2012-12-19 | 2014-06-26 | Universidade Federal De Minas Gerais - Ufmg | Óleo de girassol (helianthus annuus) modificado enzimaticamente, processo de obtenção e uso dos seus derivados como antimicrobianos |
| CN119816600A (zh) * | 2022-08-03 | 2025-04-11 | 阿胡斯卡尔斯油脂有限公司 | 用于增加植物油的sos甘油三酯含量的酶促方法 |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU2208477A (en) * | 1976-02-01 | 1978-08-17 | Unilever Ltd. | Enzyne cataysed interestification of fats |
| US4268527A (en) * | 1978-11-21 | 1981-05-19 | Fuji Oil Company, Ltd. | Method for producing cacao butter substitute |
| AU7762381A (en) * | 1981-11-18 | 1983-05-26 | Fuji Oil Company Limited | Method for modification of fats and oils |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5932119B2 (ja) * | 1976-04-08 | 1984-08-06 | 不二製油株式会社 | カカオバタ−代用脂の製造法 |
| JPS5584397A (en) * | 1978-12-20 | 1980-06-25 | Ajinomoto Kk | Fat and oil ester exchange using lipase |
| JPS5615643A (en) * | 1979-07-17 | 1981-02-14 | Fuji Oil Co Ltd | Production of hard butter |
| EP0035883B1 (en) * | 1980-03-08 | 1984-06-06 | Fuji Oil Company, Limited | Method for enzymatic interesterification of lipid and enzyme used therein |
| WO1982003873A1 (en) * | 1981-05-07 | 1982-11-11 | Halling Peter James | Fat processing |
| CA1241227A (en) * | 1981-07-08 | 1988-08-30 | Alasdair R. Macrae | Edible fat process |
| JP2841512B2 (ja) * | 1989-08-07 | 1998-12-24 | 旭硝子株式会社 | 減圧脱泡装置の監視方法及びその装置 |
-
1986
- 1986-05-06 GB GB08610979A patent/GB2190394A/en not_active Withdrawn
-
1987
- 1987-05-04 AU AU72481/87A patent/AU596411B2/en not_active Ceased
- 1987-05-05 EP EP87303996A patent/EP0245076A3/en not_active Withdrawn
- 1987-05-05 SE SE8701847A patent/SE467860B/sv not_active Application Discontinuation
- 1987-05-06 JP JP62110393A patent/JPS6317697A/ja active Granted
- 1987-05-06 ZA ZA873239A patent/ZA873239B/xx unknown
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU2208477A (en) * | 1976-02-01 | 1978-08-17 | Unilever Ltd. | Enzyne cataysed interestification of fats |
| US4268527A (en) * | 1978-11-21 | 1981-05-19 | Fuji Oil Company, Ltd. | Method for producing cacao butter substitute |
| AU7762381A (en) * | 1981-11-18 | 1983-05-26 | Fuji Oil Company Limited | Method for modification of fats and oils |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU615969B2 (en) * | 1987-10-13 | 1991-10-17 | Lubrizol Corporation, The | Method of producing cis-9-octadecenoic acid compositions |
Also Published As
| Publication number | Publication date |
|---|---|
| JPH0430836B2 (enrdf_load_stackoverflow) | 1992-05-22 |
| EP0245076A3 (en) | 1989-10-18 |
| GB8610979D0 (en) | 1986-06-11 |
| JPS6317697A (ja) | 1988-01-25 |
| SE8701847D0 (sv) | 1987-05-05 |
| SE8701847L (sv) | 1987-11-07 |
| AU7248187A (en) | 1987-11-12 |
| EP0245076A2 (en) | 1987-11-11 |
| GB2190394A (en) | 1987-11-18 |
| SE467860B (sv) | 1992-09-28 |
| ZA873239B (en) | 1989-01-25 |
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