CA1136483A - Edible fat product i - Google Patents

Edible fat product i

Info

Publication number
CA1136483A
CA1136483A CA000354417A CA354417A CA1136483A CA 1136483 A CA1136483 A CA 1136483A CA 000354417 A CA000354417 A CA 000354417A CA 354417 A CA354417 A CA 354417A CA 1136483 A CA1136483 A CA 1136483A
Authority
CA
Canada
Prior art keywords
oil
hardstock
saturated
weight
less
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired
Application number
CA000354417A
Other languages
French (fr)
Inventor
John Ward
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Conagra Brands Inc
Original Assignee
Nabisco Brands Ltd
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.)
Filing date
Publication date
Application filed by Nabisco Brands Ltd filed Critical Nabisco Brands Ltd
Priority to CA000354417A priority Critical patent/CA1136483A/en
Priority to GB8118494A priority patent/GB2078245B/en
Priority to MX819496U priority patent/MX6133E/en
Priority to IT22417/81A priority patent/IT1137091B/en
Priority to BE0/205143A priority patent/BE889291A/en
Priority to SE8103867A priority patent/SE450682B/en
Priority to FI811923A priority patent/FI68754C/en
Priority to SU813305049A priority patent/SU1523041A3/en
Priority to FR8112158A priority patent/FR2484790A1/en
Priority to AU71993/81A priority patent/AU552183B2/en
Priority to NL8102979A priority patent/NL8102979A/en
Priority to DE19813124148 priority patent/DE3124148A1/en
Priority to DK271381A priority patent/DK271381A/en
Priority to JP9411181A priority patent/JPS5725396A/en
Priority to ES503231A priority patent/ES8300249A1/en
Priority to ZA814169A priority patent/ZA814169B/en
Application granted granted Critical
Publication of CA1136483A publication Critical patent/CA1136483A/en
Expired legal-status Critical Current

Links

Classifications

    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23DEDIBLE OILS OR FATS, e.g. MARGARINES, SHORTENINGS, COOKING OILS
    • A23D7/00Edible oil or fat compositions containing an aqueous phase, e.g. margarines
    • A23D7/001Spread compositions
    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23DEDIBLE OILS OR FATS, e.g. MARGARINES, SHORTENINGS, COOKING OILS
    • A23D7/00Edible oil or fat compositions containing an aqueous phase, e.g. margarines
    • A23D7/003Compositions other than spreads
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11CFATTY ACIDS FROM FATS, OILS OR WAXES; CANDLES; FATS, OILS OR FATTY ACIDS BY CHEMICAL MODIFICATION OF FATS, OILS, OR FATTY ACIDS OBTAINED THEREFROM
    • C11C3/00Fats, oils, or fatty acids by chemical modification of fats, oils, or fatty acids obtained therefrom
    • C11C3/04Fats, oils, or fatty acids by chemical modification of fats, oils, or fatty acids obtained therefrom by esterification of fats or fatty oils
    • C11C3/10Ester interchange

Abstract

ABSTRACT OF THE DISCLOSURE

Soft margarines of both the tub and fluid type, as well as blends and spreads, are formed from a unique blend of liquid vegetable oil, such as sunflower oil, with varying proportions from about 5 to about 20 wt.% of a hardstock preferably formed by interesterification of saturated babassu nut oil and saturated palm oil. The blend of vegetable oil and hardstock is high in polyunsaturates and has a low-trans-isomer fatty acid content.

Description

~ L~ A~O~UC~ I

The present invention relates to edible ~at products, particularly to edible fat products suitable for formation into soft margarines.
5Table margarines generally have been produaed by emulsification of blends of liquid unsaturated vegetable oils with hydrogenated hardstock in varying proportions depending on the consistency of product desired. A margarine product is required to have certain flow characteristics while resisting free oil separation and-yet should- be rapidly~melting on the ~ , ~ tongue. The hydrogen~ation required to form a hardstock which - : , .
~can provide such: characteristics also leads to residual unsaturation which i5~in trans-isomeric forms of the mono-and poly-unsaturates. ~Such~;trans-isomeric forms of fatty acids in the diet are currently the center of much scientific controversy and the~ sub~eçt o~ on-going research to determine what role, if any, they play in dietary health.
In accordanae with the- present invention, a specific hardstock has been found which allevia*es this concern, while at the same time is suitable for the ~orm~lation of edible fat products for use in the production of margarines which are substantially free of trans-isomers. ~he invention, in its .
' ~ ' s 11364~3 broad aspects, provides a process for forming a low-trans-isomer-containing fat product, which comprises: preparing a randomly interesterified mixture of saturated babassu nut oil having an iodine value of less than 2.0, and a second saturated edible oil having an iodine value of less than 2.0, the mixture comprising said saturated babassu nut oil and said saturated second oil in the weight proportions of 60:40 to about 40:60, the interesterified mixture resulting in a hardstock having an SFI solids content of at least about 45 at 92F (as determined by the AOCS SFI Method); and blending said hardstock with a liquid vegetable oil in proportions such that the resulting blend contains from about 5% to about 20% by weight of said hardstock.
While it is impractical commercially to prepare a product ha~ing absolutely no determinable trans-isomer content, the present invention contemplates those products where the trans-isomer content is substantially eliminated~ Preferred products are made under suitable controls to assure a tranæ-~ isomer content of: less than 1%. The term low-trans-isomer-: 20 content~ is thue .defined accordingly. The trans-iso~er content is determined by infra-red spectrophotometry according to the official method of the Ameriaan Oil Chemists J ~
A Assoaiation ~AOCS) designated Cd-~-61.
The term "fat" as used herein is intended to inalude all edible, fatty acid triglycerides regardless of orîgin or .whether they are solid or liquid at room temperature. Thus., the term Rfat" includes normally liquid and normally solid vegetable and animal fats and oils. Where the term "oil n is employed herein, it is intended to refer to ~hose fats which are normally liquid in their unmodified state~

1~3ti4~33 The hardstock which is utilized in the present invention is a randomly interesterified mi~ture of saturated babassu nu~
oil and a saturated second oil in proportions by weight of about 75:25 to about 40:60, preferably fro~ about 60:40 to about 40:60. These oils must be saturated, having iodine values of less than 2Ø Suitable saturated fats may be obtained by hydrogenating, either in admixture or separately, or by fractionating a suitable fat. The interesterification is effected at an elevated temperature and under vacuum in the presence of a suitable catalyst to form a product having a solids content of not less than about 45~ at 92F (as determined by the AOCS SFI method) and preferably a Wiley melting point of about 112 to 120F. Preferably, the solids content at 92F will not be less than a~out 50% and the ~iley melting point will be within the range of from 115 to 119F.
Completion of the interesterification reaction usually is determined by a 10F lowering of the melt point of the product as co~pared to the mixture prior to interesterification.
It is also possible to form the hardstock by first interesterifying the specified oils and then hydrogenating to the ~equired degree of~ saturation. The latter procedure, however, is less preferred since completion of the interesterification i9 less susceptible to precise determination than in the case when the interesterification is effected after saturation of materials.
Essential to the present invention is the use as starting material of babassu nut oil, i.e., the oil from the babassu nut At~alea funifera. The use of thiæ material results in a hardstock which enables margarines of varying consistencies 113f~4~33 and yet acceptable properties to be provided while at the same time permits the use of conventional processing, packaging, and equip~ent.
Also essential to the present invention is the use as a starting material of a second edible oil saturated to an iodine value of less than 2.0 which preferably has a melting point of from about 55 to about 60C. This second oil is interesterified with the saturated babassu nut oil, resulting in a hardstock which contains no residual trans-unsaturation.
It is within the scope of the invention to utilize suitable animal and vegetable fats which are saturated to have iodine values of less than 2.0 with pree~able melting points of between about 55 and 60C. These materials will provide a desirable range of physical properties and be free of trans-unsaturation. Among the suitable fats are those of animal and vegetable origin which are capable of providing these prop~rties when saturated, but in their natural state, prior to any hydrogenation, exhibit iodine values of less than about 60, preferably less than about 50.
~20 Biends or fractions of vegetable fats including palm oil, and coconut oil; and animal fats such as tallow, can be employed where th~y meet the above criteria. The preferred vegetable fat according to the invention comprises palm oil, and the preferred ani~al fat comprises tallow.
The requisite low-trans fat of the present invention is not achieved when the second edible oil comprises an unsaturated oil such as rapeseed oil [Canola oil], cottonseed oil, soyabean oil or a highly unæaturated fraction of these or other fats. ~hen such fats are employed and the hydrogenation 113~4~33 is continued to the point necessary to yield the ~elting point range of 55 to 60C, trans-isomer contents detectable in amounts significantly greater than 1% remain. And, where hydrogenation is effected to result in saturation with a correspondingly higher melting point, the interesterification product is incapable of providing an edible fat product having the preferred SFI values.
In the mar~.et place, margarines are generally sold as one of two principal types, namely, print, hard or stick margarine and soft or tub margarine. Hard or stick margarine would have a firmness consistent with a penetration range of 65 to 120 being in units of 0.1 mm using an AS~M grease cone at 45F.
Soft or tub margarine would have a firmness consistent with a penetration range of 130 to 210 being in units of 0.1 mm using an ASTM grease cone at 45F. Lesser amounts of margarine are sold in a form so soft that it is fluid, being at least capable of being squeezed from a flexible container. The present invention is directed to the production of edible fat products suitable for use in the tub and fluid forms. It is also within the contemplation of the invention that the fat products of the invention can be employed in the preparation of calorie-reduced margarine ~diet margarine), industrial shortenings, blends with dairy products and spreads containing less than 80% fat.
The SFI solids values required for an edible fat to be used in formulation of a tub margarine are a minimu~ solids content of 9~ at 50F, a minimum solids content of 5% at 70F
and a maximum solids content of 4~ at 92F. Preferably, the maximum solids content at 50F will be less than 12%, at 70F

.
. .

113~4~3 will be less than 7%, and will be less than 3% at 92F. Most preferably, the maximum solids content at 92F will be about
2%. A margarine formed from an edible fat product of this specification is easily spread at room temperature without substantial oil separation, and yet a good mouth break at about 96F results. Such a product may be formulated, in accordance with this invention, fro~ an edible fat product which is a blend of liquid unsaturated vegetable oils and the hardstock containing about 5 to about 20 wt.% of the hardstock, preferably from 14 to 20 wt.%, most preferably above 15, typically from about I6 to about 19 wt.%.
For squeezable fluid spreads having a minimum hardstock content of 5 wt.%, the SFI solids values should be near the lower ends of the above ranges and are preferably just below them having, for example, a minimum solids content of 2% at 50F, a minimu~ solids content of 1% at 70F, and a maximum solids content of 1% at 92F. Preferably, the ~aximum solids content at 50F wlll be 5% and at 70F will be~3%.
It has previously been suggested in United States Patent No. 3,617,308 to use, in the for~ulation of margarines, a randomly interesterified product of a ~i*ture of fully hardened palm kernel oil and a fully hardened vegetable oil, such as palm oil, rapeseed oil tCanola oil], cottanseed oil, or soyabean oil. The blends of resulting hardstock with liquid vegetable oil contain 8 to 15 wt.%, preferably 8 to 12 wt.~ of the hardstock. One key starting material in that patent is pal~ kernel oil, i.e., the oil fro~ the kernel of the palm fruit Elaeis quineensis, a quite different starting material fro~ that used in this invention, where babassu nut oil is used. This patent is not concerned with the production 11364~33 of a low-trans-isomer-content fat, and in fact of the various hardened vegetable oils which may be used to form the interesterification product, only palm oil is suitable for forming a product having no trans-unsaturation. The soyabean oil, rapeseed oil [Canola oil~ and cottonseed oil when hardened to only 55C, the low end of the slip-point range set forth in the Patent, contain detectable amounts of trans-isomers.
The ability to formulate an edible fat product containing up to 95 wt.% of liquid vegetable oil enables high levels of polyunsaturates to be attained both in tub and fluid formulations in this invention. In qeneral, higher polyunsaturate levels in the margarine may be attained than in conventionally-formulated margarines, and, at the same time, trans-unsaturated isomers are absent from the product.
A wide variety of edible liquid vegetable oils may be used in formulating the edible fat product from the interesterified hardstock, includinq safflower oil, sunflower oil, soyabean oil, corn oil, cottonseed oil, rapeseed oil ~Canola oil], peanut oil, linseed oil, wheat germ oil. The liquid vegetable oils most suitable have a ratio of polyunsaturates to saturates (P/S) of greater than 2:1.
The fat blends provided in accordance with this invention may be emulsified to form margarines in conventional manner, as well as to form blends and spreads. Typically, the edible fat product is emulsified with an aqueous phase at an elevated temperature at which the fat product is liquid and then subjected to rapid chilling. This procedure may be effecte~
using apparatus of conventional kind comprising one or more , 113~4~3 scraped surface tubular heat exchangers, for instance, "votator" apparatus, wherein the emulsion is worked up to form a water-in-oil emulsion of suitable consistency for spreading.
The super-cooled emulsion is filled into suitable containers.
If desired, the initial liquid fat mixture may be subjected to a crystallizing step, either before or after emulsification or, before the final chilling step, and further crystallization may be effected, for example, in resting or working units, such as Votator B-units or whipping units, before filling or forming the plastic emulsion into containers. Additionally, the plastic emulsion may be worked mechanically between the resting or working units and the filling or forming device.
The invention is illustrated further by the following examples:
. . -Example 1 This example illustrate4 the formation of low-trans-isomer-content~hardstock from babassu nut oil and palm oil for use in products according to the invention.
Babassu nut oil was hydrogenated at 300F using a suæpension of 0.2% nickel catalyst (26% Ni) based on the oil to an iodine value of less than 2.0 to form a saturated product of ~elting point 113F (45C). Palm oil was similarly hydrogenated using nickel catalyst to an iodine value of less than 2.0 to form a saturated product of melting point 140F
(60C). The hydrogenated materials were filtered to remove the nickel.
3~83 g The resulting saturated babassu nut oil and saturated palm oil were mixed in the weight proportion of 50:50 and steam stripped to decrease the free fatty acid content below about 0.03 wt.%. Under a high vacuum of 2 to 3 mm Hg, the mixture was heated at 250F in the presence of 0.05% sodium methoxide catalyst under agitation for 15 minutes. A sam~le of product was analysed to confirm that the interesterifi-cation was complete, as determined by 10F lowering of the melt point of the product as compared to the mixture prior to interesterification.
The temperature was then decreased to 180F and 0.4 wt.%
of a 30% aqueous solution of magnesium sulphate in hot water was added to destroy residual catalyst. The temperature was then raised to 210F and 1~ bleaching earth was added to bleach the product. Thereafter, the interesterified material is cooled and filtered.
The hardstock product produced~ was ound to have an SFI
solids value of 54.4% at 92F and a Wiley Melting point of 117.5%. In addition, ~he hardstock product was found to contain no trans-isomeric for~s, as determined by infra-red . .
spe¢trophotometry.

ExamPle 2 ~-This example shows the blending of the hardstock of Example 1 with a liquid vegetable oil and the formation of low-trans-isomer-content tub margarine from the blend.
The hardstock formed according to Example 1 was blended wi~h sunflower oil to form a blend containing 16~ by weight of the hardstock. The resulting blend had an unsaturates to 113641!~3 saturates ratio of 2.2:1 [57% polyunsaturates to 24~ saturates based on the ~otal weight of the fat], and exhibited the following SFI solids values:

9.4% at 50F
56.2% at 70F
2.0% at 92F

The blend was combined with about 20% of its weight of an aqueous phase and processed through conventional "Votator~ A
units and working B unit to form a water-in-oil emulsion which 0 i9 forwarded to conventional packaglng equipment to provide a tub margarine. The resulting margarine spread readily, did not exhibit oil separation during processing or subs~quently at room temperature, and had good mouth break. The margarine had a penetration of 160, being in units of 0.1 mm using an ASTM grease cone at 45F.

ExamPle 3 This example shows the formation of a low-trans-isomer-content hardstock formed in similar manner tD example 1 but in the weight proportion of 55% saturated babassu nut oil 45~
saturated tallow, which blend was su~sequently interesterified. The hardstock product produced was found to have an SFI solids value~ of 4S.7% at 92F and a Wiley melt point of 116F.
~n sunmary o~ this disclosure, the present invention provides an edible low-trans-isomer-content fat product which may be used in both tub and fluid margarine production.
Modifications are possible within the scope of the invention.

Claims (22)

The embodiments of the invention in which an exclusive property or privilege is claimed are defined as follows:
1. A process of forming a low-trans-isomer-containing edible fat product, which comprises:
preparing a randomly interesterified mixture of saturated babassu nut oil having an iodine value of less than 2.0 and a second saturated edible oil having an iodine value of less than 2.0, the mixture comprising said babassu nut oil and said second oil in the weight proportions of about 75:25 to about 40:60, the interesterified mixture resulting in a hardstock having an SFI solids content of at least about 45% at 92°F, and, blending said hardstock with a liquid vegetable oil in proportions such that the resulting blend contains about 5% to about 20% by weight of said hardstock.
2. The process of claim 1 wherein said second saturated edible oil has a melt point of from 55°C to 60°C.
3. The process of claim 1 wherein said hardstock has a Wiley melting point of from about 112° to about 120°F.
4. The process of claim 1 wherein said hardstock and said liquid vegetable oil are blended in such proportions that the resulting blend exhibits SFI solids contents of at least 9% at 50°F, at least 5% at 70°F and a maximum of 3% at 92°F.
5. The process of claim 4 wherein said blend contains about 14 to 20% by weight of said hardstock.
6. The process of claim 5 wherein said blend contains above 15% by weight of said hardstock.
7. The process of claim 6 wherein said blend contains from about 16 to about 19% by weight of said hardstock.
8. The process of claim 4 wherein said resulting blend exhibits SFI content maximum of 12% at 50°F and 7% at 70°F.
9. The process of claim 1 wherein the saturated babassu nut oil is prepared by hydrogenation.
10. The process of claim 1 wherein the saturated babassu nut oil is obtained by fractionation of babassu nut oil.
11. The process of claim 1 wherein said saturated second oil is prepared by hydrogenation.
12. The process of claim 1 wherein said second oil comprises a fat of vegetable or animal origin which prior to any hydrogenation exhibits an iodine value of less than about 60.
13. The process of claim 12 wherein said second oil prior to hydrogenation exhibits an iodine value of less than about 50.
14. The process of claim 13 wherein said second oil comprises a member selected from the group consisting of palm oil, coconut oil, tallow and combinations of these.
15. The process of claim 14 wherein the second oil comprises palm oil or tallow.
16. The process of claim is wherein the second oil consists essentially of palm oil.
17. The process of claim 1 wherein said second oil is obtained by fractionation of that oil.
18. The process of claim 1 wherein said liquid vegetable oil comprises a member selected from the group consisting of safflower oil, sunflower oil, soyabean oil, corn oil, cottonseed oil, rapeseed (Canola) oil, peanut oil, linseed oil, wheat germ oil.
l9. The process of claim 1 wherein the hardstock has an SFI
solids content of at least about 50% at 92°F.
20. The process of claims 4, 5, 6, 14, or 18 including forming said blend into a tub margarine.
21. A low-trans-isomer containing edible fat product comprising a blend of about 5 to about 20% by weight of a hardstock and the balance by weight of liquid vegetable oil, the hardstock having an SFI solids content of at least about 45% at 92°F, said hardstock being a randomly interesterified mixture of saturated babassu nut oil having an iodine value of less than 2.0 and a second saturated edible oil having an iodine value of less than 2.0, the mixture comprising said babassu nut oil and said second oil in the weight proportions of about 75:25 to about 40:60.
22. A low-trans-isomer margarine which comprises a water-in-oil emulsion wherein the oil phase comprises a blend of about 5 to about 20% by weight of a hardstock and the balance by weight of liquid vegetable oil, the hardstock having an SFI
solids content of at least about 45% at 92°F, said hardstock being a randomly interesterified mixture of saturated babassu nut oil having an iodine value of less than 2.0 and a second saturated edible oil having an iodine value of less than 2.0, the mixture comprising said babassu nut oil and said second oil in the weight proportions of about 75:25 to about 40:60.
CA000354417A 1980-06-19 1980-06-19 Edible fat product i Expired CA1136483A (en)

Priority Applications (16)

Application Number Priority Date Filing Date Title
CA000354417A CA1136483A (en) 1980-06-19 1980-06-19 Edible fat product i
GB8118494A GB2078245B (en) 1980-06-19 1981-06-16 Intersterified oils and margarines containing such oils
MX819496U MX6133E (en) 1980-06-19 1981-06-17 PROCEDURE FOR THE ELABORATION OF AN EDIBLE FAT WITH LOW CONTENT OF TRANS-ISOMERS, SUITABLE FOR THE MANUFACTURE OF SOFT MARGARINES
BE0/205143A BE889291A (en) 1980-06-19 1981-06-18 EDIBLE FATTY PRODUCT AND PROCESS FOR PREPARING THE SAME
SE8103867A SE450682B (en) 1980-06-19 1981-06-18 HARD FAT, METHOD OF PRODUCING THEREOF, AND ITS APPLICATION FOR SOME FAT PRODUCTS WITH A TRANSISOMER CONTENT OF LESS THAN 1 PERCENT
FI811923A FI68754C (en) 1980-06-19 1981-06-18 FOERFARANDE FOER FRAMSTAELLNING AV EN NAERINGSFETTPRODUKT INNEHAOLLANDE KNAPPT AV TRANS-ISOMERER
SU813305049A SU1523041A3 (en) 1980-06-19 1981-06-18 Method of producing fat mixture for edible fat manufacture
IT22417/81A IT1137091B (en) 1980-06-19 1981-06-18 PRODUCT CONSTITUTED FROM AN EDIBLE FAT
FR8112158A FR2484790A1 (en) 1980-06-19 1981-06-19 EDIBLE FATTY PRODUCT AND PROCESS FOR PREPARING THE SAME
AU71993/81A AU552183B2 (en) 1980-06-19 1981-06-19 Edible fat hardstock
NL8102979A NL8102979A (en) 1980-06-19 1981-06-19 EDIBLE FAT PRODUCT.
DE19813124148 DE3124148A1 (en) 1980-06-19 1981-06-19 EDIBLE FAT PRODUCT AND METHOD FOR THE PRODUCTION THEREOF
DK271381A DK271381A (en) 1980-06-19 1981-06-19 HARD FAT AND PROCEDURE FOR PREPARING THEREOF
JP9411181A JPS5725396A (en) 1980-06-19 1981-06-19 Edible fat product
ES503231A ES8300249A1 (en) 1980-06-19 1981-06-19 Interesterfied Oils and Margarines Containing Such Oils
ZA814169A ZA814169B (en) 1980-06-19 1981-06-19 Edible fat product 1.

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CA000354417A CA1136483A (en) 1980-06-19 1980-06-19 Edible fat product i

Publications (1)

Publication Number Publication Date
CA1136483A true CA1136483A (en) 1982-11-30

Family

ID=4117220

Family Applications (1)

Application Number Title Priority Date Filing Date
CA000354417A Expired CA1136483A (en) 1980-06-19 1980-06-19 Edible fat product i

Country Status (16)

Country Link
JP (1) JPS5725396A (en)
AU (1) AU552183B2 (en)
BE (1) BE889291A (en)
CA (1) CA1136483A (en)
DE (1) DE3124148A1 (en)
DK (1) DK271381A (en)
ES (1) ES8300249A1 (en)
FI (1) FI68754C (en)
FR (1) FR2484790A1 (en)
GB (1) GB2078245B (en)
IT (1) IT1137091B (en)
MX (1) MX6133E (en)
NL (1) NL8102979A (en)
SE (1) SE450682B (en)
SU (1) SU1523041A3 (en)
ZA (1) ZA814169B (en)

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2178752B (en) * 1985-07-12 1989-10-11 Unilever Plc Substitute milk fat
JPH0643595B2 (en) * 1985-10-03 1994-06-08 不二製油株式会社 Method for producing fat composition
GB8711431D0 (en) * 1987-05-14 1987-06-17 Unilever Plc Edible fats
US5407695A (en) * 1989-09-20 1995-04-18 Nabisco, Inc. Low-palmitic, reduced-trans margarines and shortenings
IE940671A1 (en) * 1993-08-31 1995-03-08 Charleville Res An edible fat blend
CA2156103A1 (en) * 1994-09-09 1996-03-10 Michael David Erickson Fat systems and processes for the production of no trans fatty acid containing stick-type margarines and spreads
JP3743179B2 (en) * 1998-10-28 2006-02-08 株式会社カネカ Oil composition
RU2609374C2 (en) * 2015-06-16 2017-02-01 Общество С Ограниченной Ответственностью "Корпорация "Союз" Functional triglyceride composition for production of food products
RU2612446C2 (en) * 2015-08-18 2017-03-09 Общество с ограниченной ответственностью "ЭФКО Пищевые Ингредиенты" Method for producing hydrogenated fat and milk fat substitute on its base, as well as hydrogenated fat and substitute of milk fat

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1107206A (en) * 1964-12-28 1968-03-27 Nat Biscuit Co Hard butter and chocolate coating composition containing same
FR1537038A (en) * 1966-06-28 1968-08-23 Unilever Nv Fat with a high content of polyunsaturated fatty acids
GB1190553A (en) * 1966-06-28 1970-05-06 Unilever Nv Improvements in Fats
GB1382573A (en) * 1971-01-06 1975-02-05 Unilever Ltd Confectioners butter

Also Published As

Publication number Publication date
ZA814169B (en) 1982-07-28
NL8102979A (en) 1982-01-18
SE450682B (en) 1987-07-20
FI68754C (en) 1985-11-11
ES503231A0 (en) 1982-11-01
FI68754B (en) 1985-07-31
SU1523041A3 (en) 1989-11-15
BE889291A (en) 1981-12-18
IT1137091B (en) 1986-09-03
DK271381A (en) 1982-02-03
FR2484790B1 (en) 1985-03-29
IT8122417A0 (en) 1981-06-18
MX6133E (en) 1984-11-22
DE3124148A1 (en) 1982-03-04
GB2078245A (en) 1982-01-06
SE8103867L (en) 1981-12-20
JPS5725396A (en) 1982-02-10
FI811923L (en) 1981-12-20
AU7199381A (en) 1981-12-24
GB2078245B (en) 1984-11-28
AU552183B2 (en) 1986-05-22
ES8300249A1 (en) 1982-11-01
FR2484790A1 (en) 1981-12-24

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