IES85011Y1 - Food products - Google Patents
Food productsInfo
- Publication number
- IES85011Y1 IES85011Y1 IE2007/0761A IE20070761A IES85011Y1 IE S85011 Y1 IES85011 Y1 IE S85011Y1 IE 2007/0761 A IE2007/0761 A IE 2007/0761A IE 20070761 A IE20070761 A IE 20070761A IE S85011 Y1 IES85011 Y1 IE S85011Y1
- Authority
- IE
- Ireland
- Prior art keywords
- weight
- food product
- mono
- diglycerides
- fatty acids
- Prior art date
Links
- 235000013305 food Nutrition 0.000 title claims abstract description 38
- 239000012071 phase Substances 0.000 claims description 23
- 239000007787 solid Substances 0.000 claims description 11
- 238000002425 crystallisation Methods 0.000 claims description 9
- 230000005712 crystallization Effects 0.000 claims description 9
- 239000000203 mixture Substances 0.000 claims description 8
- 239000001788 mono and diglycerides of fatty acids Substances 0.000 claims description 8
- 235000010935 mono and diglycerides of fatty acids Nutrition 0.000 claims description 8
- -1 organic acid ester Chemical class 0.000 claims description 8
- 239000001791 acetic acid esters of mono and diglycerides of fatty acids Substances 0.000 claims description 7
- 239000008346 aqueous phase Substances 0.000 claims description 7
- 150000004670 unsaturated fatty acids Chemical group 0.000 claims description 7
- 239000003795 chemical substances by application Substances 0.000 claims description 6
- 239000001792 lactic acid esters of mono and diglycerides of fatty acids Substances 0.000 claims description 4
- 239000001937 mono and diacetyl tartraric acid esters of mono and diglycerides of fatty acids Substances 0.000 claims description 4
- 239000002273 mixed acetic and tartraric acid esters of mono and diglycerides of fatty acids Substances 0.000 claims description 3
- 239000001793 Citric acid esters of mono and diglycerides of fatty acids Substances 0.000 claims description 2
- 235000010937 acetic acid esters of mono- and di- glycerides of fatty acids Nutrition 0.000 claims description 2
- 235000010938 lactic acid esters of mono- and di- glycerides of fatty acids Nutrition 0.000 claims description 2
- 235000010961 mono- and di- acetyl tartraric acid esters of mono- and di- glycerides of fatty acids Nutrition 0.000 claims description 2
- 150000002168 ethanoic acid esters Chemical class 0.000 claims 1
- 235000015067 sauces Nutrition 0.000 abstract description 3
- 239000003925 fat Substances 0.000 description 40
- 235000019197 fats Nutrition 0.000 description 40
- 235000019482 Palm oil Nutrition 0.000 description 16
- 239000002540 palm oil Substances 0.000 description 16
- 230000000052 comparative effect Effects 0.000 description 11
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 9
- 239000003921 oil Substances 0.000 description 9
- 235000019198 oils Nutrition 0.000 description 9
- 235000013310 margarine Nutrition 0.000 description 8
- 239000004615 ingredient Substances 0.000 description 7
- 239000003264 margarine Substances 0.000 description 7
- FAPWRFPIFSIZLT-UHFFFAOYSA-M sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 6
- 239000003549 soybean oil Substances 0.000 description 6
- 235000012424 soybean oil Nutrition 0.000 description 6
- 240000001889 Brahea edulis Species 0.000 description 5
- 239000000796 flavoring agent Substances 0.000 description 4
- 239000000523 sample Substances 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- BVDRUCCQKHGCRX-UHFFFAOYSA-N 2,3-dihydroxypropyl formate Chemical compound OCC(O)COC=O BVDRUCCQKHGCRX-UHFFFAOYSA-N 0.000 description 3
- 229940069338 Potassium Sorbate Drugs 0.000 description 3
- CHHHXKFHOYLYRE-STWYSWDKSA-M Potassium sorbate Chemical compound [K+].C\C=C\C=C\C([O-])=O CHHHXKFHOYLYRE-STWYSWDKSA-M 0.000 description 3
- 235000014113 dietary fatty acids Nutrition 0.000 description 3
- 239000000194 fatty acid Substances 0.000 description 3
- 150000004665 fatty acids Chemical class 0.000 description 3
- 235000019634 flavors Nutrition 0.000 description 3
- 238000005259 measurement Methods 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 239000004302 potassium sorbate Substances 0.000 description 3
- 235000010241 potassium sorbate Nutrition 0.000 description 3
- 239000011780 sodium chloride Substances 0.000 description 3
- POULHZVOKOAJMA-UHFFFAOYSA-N Lauric acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 2
- OYHQOLUKZRVURQ-IXWMQOLASA-N Linoleic acid Natural products CCCCC\C=C/C\C=C\CCCCCCCC(O)=O OYHQOLUKZRVURQ-IXWMQOLASA-N 0.000 description 2
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N Oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 2
- IPCSVZSSVZVIGE-UHFFFAOYSA-N Palmitic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 2
- QIQXTHQIDYTFRH-UHFFFAOYSA-N Stearic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 125000004432 carbon atoms Chemical group C* 0.000 description 2
- 150000001746 carotenes Chemical class 0.000 description 2
- 235000005473 carotenes Nutrition 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000003995 emulsifying agent Substances 0.000 description 2
- 238000009884 interesterification Methods 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 235000014593 oils and fats Nutrition 0.000 description 2
- 239000003346 palm kernel oil Substances 0.000 description 2
- 235000019865 palm kernel oil Nutrition 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 235000019871 vegetable fat Nutrition 0.000 description 2
- 241000251468 Actinopterygii Species 0.000 description 1
- 208000004981 Coronary Disease Diseases 0.000 description 1
- 239000004150 EU approved colour Substances 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- 239000005639 Lauric acid Substances 0.000 description 1
- 229940067606 Lecithin Drugs 0.000 description 1
- 239000005642 Oleic acid Substances 0.000 description 1
- 235000021314 Palmitic acid Nutrition 0.000 description 1
- 235000019484 Rapeseed oil Nutrition 0.000 description 1
- 235000019485 Safflower oil Nutrition 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- 235000019486 Sunflower oil Nutrition 0.000 description 1
- 210000004243 Sweat Anatomy 0.000 description 1
- 238000006640 acetylation reaction Methods 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 239000010775 animal oil Substances 0.000 description 1
- 239000006172 buffering agent Substances 0.000 description 1
- 239000000828 canola oil Substances 0.000 description 1
- 235000019519 canola oil Nutrition 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 239000003240 coconut oil Substances 0.000 description 1
- 235000019864 coconut oil Nutrition 0.000 description 1
- 201000008739 coronary artery disease Diseases 0.000 description 1
- 235000012343 cottonseed oil Nutrition 0.000 description 1
- 239000002385 cottonseed oil Substances 0.000 description 1
- 230000001419 dependent Effects 0.000 description 1
- 230000003292 diminished Effects 0.000 description 1
- 239000008157 edible vegetable oil Substances 0.000 description 1
- 235000013355 food flavoring agent Nutrition 0.000 description 1
- 238000005194 fractionation Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 238000005984 hydrogenation reaction Methods 0.000 description 1
- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- 239000011630 iodine Substances 0.000 description 1
- 239000000787 lecithin Substances 0.000 description 1
- 235000010445 lecithin Nutrition 0.000 description 1
- 235000020778 linoleic acid Nutrition 0.000 description 1
- 235000010966 mixed acetic and tartraric acid esters of mono- and di- glycerides of fatty acids Nutrition 0.000 description 1
- 235000021313 oleic acid Nutrition 0.000 description 1
- 229940006093 opthalmologic coloring agents Diagnostic Drugs 0.000 description 1
- 238000004806 packaging method and process Methods 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 230000002335 preservative Effects 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 102000004169 proteins and genes Human genes 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 235000021067 refined food Nutrition 0.000 description 1
- 239000003813 safflower oil Substances 0.000 description 1
- 235000005713 safflower oil Nutrition 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 238000004904 shortening Methods 0.000 description 1
- 238000003892 spreading Methods 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000002600 sunflower oil Substances 0.000 description 1
- 239000003760 tallow Substances 0.000 description 1
- 235000010692 trans-unsaturated fatty acids Nutrition 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23D—EDIBLE OILS OR FATS, e.g. MARGARINES, SHORTENINGS, COOKING OILS
- A23D7/00—Edible oil or fat compositions containing an aqueous phase, e.g. margarines
- A23D7/01—Other fatty acid esters, e.g. phosphatides
- A23D7/011—Compositions other than spreads
Abstract
ABSTRACT This invention relates to food products, such as fillings, pastes, sauces, shortenings, toppings and spreads.
Description
This invention relates to food products, such as fillings, pastes, sauces,
shortenings, toppings and spreads.
Fat spreads have traditionally been produced using partially hydrogenated
vegetable fats and oils, to achieve a spread having good organoleptic properties.
However, such spreads generally include a substantial amount of trans unsaturated
fatty acid residues. The consumption of trans unsaturated fatty acid residues, also
known as “trans fats", is considered to have negative health implications such as
increasing the risk of coronary heart disease. This has led consumers to seek
spreads containing reduced quantities of “trans fats”, or which are substantially
free of “trans fats”, i.e. so-called “trans free” products.
“Trans free” food products can be produced by using non-hydrogenated fats and
oils. The production of “trans free” food products where a certain level of solid fat
is required e.g. margarine, can be approached in a number of ways. For example, a
fully hydrogenated oil can be blended with a liquid oil. Alternatively, this mixture
can be given a further subsequent treatment e. g. interesterification. This will have
the effect of improving the crystallisation characteristics compared to the starting
blend. However, the crystallisation behaviour is still not optimal in most cases.
Other fat phases having low or zero “trans fats” can be formulated by the use of
naturally hard, or naturally solid fat containing fat and oil sources e. g. palm oil and
palm oil fractions.
However, the disadvantage of these fat phases is that they are considered to have
poor crystallisation behaviour, resulting in the food product having one or more of
the following organoleptic aspects: a poor texture, a poor mouthfeel, brittleness, a
matt appearance, roughness, sandiness and graininess. “Sandiness" results in an
undesirable sandy, dry mouthfeel, whereas “graininess” refers to the presence of
larger, visible grains or crystals present in the spread. For this reason, oils which
are non-hydrogenated and non-interesterified in their natural form, e.g. palm oil,
have been found to be generally unsuitable for use as a fat phase in fat spreads.
It is therefore an object of the present invention to overcome or substantially
alleviate the aforementioned problems.
According to the invention there is provided a food product comprising:
(a) from about 10% to 90% by weight of a fat phase comprising:
(i) from about 95% to 99.9% by weight of the fat phase of a fat base
having a solids profile characterised by a N5-value of from about 3 to
75, and a N40-value of from about 0 tol5; and
(ii) from about 0.1% to 5% by weight of the fat phase of a crystallisation
modifying agent comprising at least one organic acid ester of mono-
and diglycerides of fatty acids; and
(b) from about 10% to 90% by weight of an aqueous phase;
wherein the food product comprises no more than 3% by weight of trans
unsaturated fatty acid residues based on the weight of the food product.
As used herein, the term “solids profile”, also referred to as a N-line, is intended to
define the melting characteristics of a fat or a fat-like substance, in this case, the
melting characteristics of the fat base of the fat phase. The N—1ine is the graph of
N-values versus the temperature T. The N-value is measured by NMR and is a
direct measure of the level of solid fat content at temperature T. For example, a
N5-value is a direct measure of the level of solid fat content measured by NMR at
°C. An appropriate procedure is described in Fette, Seifen, Anstrichmittel 80(5),
180-186 (1978). The solids profiles referred to herein relate to the overall fat base,
and accordingly, when the fat base comprises more than one component, the solids
profile of the fat base refers to the combined components and not to single
components in the fat base. To some extent N-values of fats and fatty substances
are dependent on the temperature history in the preparation of the samples for the
N-value measurement. For the purposes of the present invention, a suitable
preparatory temperature history comprises heating the sample to 80°C, followed
by 5 minutes at 60°C and 60 minutes at 0°C, whereafter the sample is held for 30
minutes at the temperature of the N-value measurement, subsequent to which said
measurement is immediately carried out.
The invention also provides the use of an organic acid ester of mono- and
diglycerides of fatty acids for improving the organoleptic properties of a food
product according to the invention.
Improving the organoleptic properties of a food product according to the invention
includes, for example, improving the texture by reducing the sandiness and/or
graininess and/or brittleness, and improving the appearance by increasing the shine
and/or smoothness.
In the food product of the invention, the fat phase is preferably present in an
amount of from about 20% to 80%, more preferably from about 30% to 70%, most
preferably from about 35% to 65%, especially approximately 60% by weight of
the food product.
The fat base in the food product of the invention preferably has a solids profile
characterised by a N5-value of from about 5 to 70, and a N40-value of from about 0
tol3, more preferably a N5-value of from about 7 to 65, and a N4o—value of from
about0 to 11.
The fat base used in the present invention may comprise one or more of the
following: marine oils and fats, animal oils and fats, and edible vegetable oils and
fats, optionally modified by fractionation and/or hydrogenation and/or
interesterification. Sources may include palm oil, rapeseed oil, soybean oil, palm
kernel oil, sunflower oil, coconut oil, cottonseed oil, canola oil and safflower oil,
tallow, lard, fish and mixtures thereof. Soybean oil and palm oil are preferred,
especially palm oil which is non-hydrogenated and non-interesterified.
Palm oil is a natural fat, which is not hydrogenated nor interesterified in its natural
form, and is trans fatty acid free. This confers on it a clean label as far as
ingredients listing on consumer packages is concerned. This is of great interest to
the general public, who are increasingly looking for more wholesome and less
processed foods. Traditionally, the use of palm oil in its natural form in margarines
and fat spreads has been very limited due to the difficulty in crystallising it in a
form which is appealing to the consumer. An appealing appearance is
characterised by a uniform appearance or smoothness when spread, shininess and
gloss, and a general ease of use especially when the margarine or spread is used
directly from the refrigerator.
Traditionally, partially hydrogenated fats (e.g. palm oil M.P. 44) have been used,
which have a high content of trans fatty acids, and therefore margarine spreads
using such hydrogenated palm oil are undesirable. Alternatively, fully
hydrogenated fats e. g. palm oil and palm kernel oil were interesterified to produce
hardstocks for margarine production. Both of these have the disadvantage that they
are perceived as being too processed in the eyes of the consumer. It has now
unexpectedly been found that margarine can be made from non-hydrogenated and
non-interesterified oil, e.g. palm oil, in its natural form.
The crystallisation modifying agent is preferably present in the fat phase in an
amount of from about 0.2% to 4%, more preferably from about 0.3% to 3%, most
preferably approximately 1.5% by weight of the fat phase.
The crystallisation modifying agent used in the invention comprises at least one
organic acid ester of mono- and diglycerides of fatty acids which is preferably
selected from: (i) acetic acid esters of mono- and diglycerides of fatty acids, also
known as ACETEM (E 472a); (ii) lactic acid esters of mono- and diglycerides of
fatty acids, also known as LACTEM (E 472b); (iii) citric acid esters of mono- and
diglycerides of fatty acids, also known as CITREM (E 4720); and (iv) mono- and
diacetyl tartaric acid esters of mono- and diglycerides of fatty acids, also known as
DATEM (E 472e); (V) mixed acetic and tartaric acid esters of mono- and
diglycerides of fatty acids, also known as MATEM (E 472f), and mixtures thereof.
Acetic acid esters of mono- and diglycerides of fatty acids are preferred, more
preferably those having an acetylation degree in the range of 0.3 to 0.7, especially
0.5. Particularly preferred are acetic acid esters of mono- and diglycerides of fatty
acids sold under the trade name Myvacet LG K available from Kerry Bio-Science,
Netherlands.
The organic acid ester used in the present invention preferably has an iodine value
of less than 55, more preferably less then 35, most preferably less than 20,
especially less than 3. The fatty acids for use in the invention may be saturated or
unsaturated, and are preferably saturated.
The fatty acids for use in the invention preferably comprise from 12 to 24 carbon
atoms, preferably from 12 to 18 carbon atoms, and are preferably selected from
lauric acid, palmitic acid, stearic acid, oleic acid and linoleic acid, and mixtures
thereof.
The aqueous phase in the food product of the invention is preferably present in an
amount of from about 20% to 80%, more preferably from about 30% to 70%, most
preferably from about 35% to 65%, especially approximately 40% by weight of
the food product.
The food product of the invention comprises no more than 3% by weight of trans
unsaturated fatty acid residues, preferably no more than 2.5% by weight of trans
unsaturated fatty acid residues based on the weight of the food product.
The food product of the invention may include one or more conventional additives
such as emulsifiers, preservatives, stabilisers, colouring agents, flavouring agents,
proteins and buffering agents. The additives may be added in varying amounts, as
will be known by persons skilled in the art, typically from about 0.01% to about
% of the fat phase and from about 0.01% to about 10% of the aqueous phase.
The food product of the invention preferably comprises no more than one grain per
cmz, more preferably no grains per cmz, wherein grains refers to grains or large
crystals clearly visible in the prepared food product.
The food product of the invention may be a filling, a paste, a sauce, a shortening, a
topping or a spread.
The invention is illustrated in the following Examples.
Examples 1 and 2
Food products according to the invention, which are spreads were prepared from
the ingredients listed in Table 1:
Table 1
Ingredients Ingredients
(Exampleg) Exam le 2
Fat Phase Fat Phase
soybean oil 30% palm oil 40%
Hardstock 30% -
Lecithin 0.1% -
Myvacet LG K 1.0% Myvacet LG K 1.0%
1% natural 0.1% 1% natural 0.1%
carotene dispersion carotene dispersion
Aqueous phase Aqueous Phase
NaCl 1.0% NaCl 1.0%
Potassium sorbate 0.03% Potassium Sorbate 0.02%
citric acid, 1 aq. 0.03% Citric acid, laq 0.02%
Water up to 100% Water up to 100%
The hardstock was a blend of liquid soybean oil and fully hardened soybean oil, which had been
chemically interesterificd.
Myvacet LG K is the trade name for acetic acid esters of mono- and diglycerides of fatty acids (E
) available from Kerry Bio-Science, Netherlands.
The food products were prepared as follows. The ingredients of the fat phase were
mixed and heated until molten. The NaCl, potassium sorbate and citric acid were
dissolved/dispersed in the water. The aqueous phase was subsequently slowly
added to the fat phase whilst being stirred, at a temperature of approximately
45°C. The composition was then processed in a pilot plant scraped surface heat
exchanger (SSHE, outlet temperature 116°C, RPM 800,), with a pin working unit
attached. The processing conditions were as follows: product throughput 6.4kg/hr
for Example 1 (pump setting 6), and 3.4 and 5.0 kg/hr for Example 2 (pump
settings 4 and 6 respectively), and the pin worker had an outlet temperature of 20-
24°C and operated at an RPM of 200. The food products were then packed and
stored in a refrigerator at 5°C. The amount of trans unsaturated fatty acid residues
present in the food product was 2.07% for Example 1, and 0.16% for Example 2
based on the weight of the food product.
Example 3
Comparative spread A was prepared from the ingredients in Table l for Example 1
and according to the procedure of Example 1 except that the 1.0% of Myvacet LG
K was replaced by 0.25% distilled monoglyceride made from palm oil (trade name
Myverol 18-04 K, available from Kerry Bio-Science, Netherlands). In spread A,
the remaining 0.75% was made up of 0.375% soybean oil and 0.375% hardstock.
The amount of 0.25% of Myverol 18-04 K used in spread A is a typical amount of
emulsifier used in margarine and spreads. Using substantially more than 0.25%,
especially more than 0.5% of Myverol 18-04 K, would have a significant negative
effect on the spread. For example, a spread produced using more than 0.5% of
Myverol 18-04 K would have an undesirable, waxy mouthfeel, and the flavour of
the spread would be diminished due to the slow release of flavours by the spread.
In contrast, using 1.0% of Myvacet LG K, as in the spread according to the
invention (Example 1), surprisingly produces a spread having a desirable
mouthfeel and good flavour.
A thin layer of the spread according to the invention (Example 1) and spread A
was spread on a sheet of paper with a knife. The number of grains in each spread
was counted and their size evaluated. The results are shown in Table 2.
Table 2
No. of Size of grains
grains/cmz of (mm)
spread
Example I 0 0
Comparative 2 — 8 0.3 — 3.0
Spread A
O The appearance of each spread was evaluated by a trained panel of eight judges,
and the results are shown in Table 3.
S
Panel list Example 1 Comparative Spread A
1 1 3
2 1 4
3 1 4
4 1 3
2 3
6 1 4
7 l 3
8 2 4
Total Score 10 30
= very smooth, no imperfections or unevenness or interruptions
= very small imperfections or unevenness or interruptions
: moderate imperfections or unevenness or interruptions
= large imperfections or unevenness or interruptions
= imperfections or unevenness or interruptions which make the spread unusable,
and/or with oil and/or water separation
Texture analysis was performed on each spread using a Texture Analyser
TA.XTplus from Stable Micro Systems. The texture of each spread was measured
at 5°C. The speed of penetration of the probe into each spread was 1 mm per
second. The probe was allowed to move down 15 mm into each spread. The
Figure illustrates that spread A had a brittle and hard texture, whereas the spread
according to the invention (Example 1) had a smooth and soft texture, thus having
the desired properties for a spread.
The comparative spread A had a matt, coarse appearance and included visible
grains, whereas the spread according to the invention exhibited a smooth
spreading texture without any grains, and was shiny in appearance. The spread
according to the invention (Example 1) also exhibited a smooth and stable
consistency on packing, and immediately after packing did not shrink from the
sides of the packaging, nor sweat or exude oil on the surface during storage at 5°C.
Example 4
Comparative spreads B and C were prepared from the ingredients in Table 1 for
Example 2 and according to the procedure of Example 2, except:
(1) without using the 1.0% of Myvacet LG K (comparative spread B); or
(2) replacing the 1.0% of Myvacet LG K by 1.0% distilled monoglyceride
(trade name Myverol 18-04 K, available from Kerry Bio-Science,
Netherlands) (comparative spread C).
The product throughput was 3.4 and 5.0 kg/hr for both comparative spreads B and
C (using pump settings 4 and 6 respectively).
The solid fat content of the fat used in Example 2 and in comparative spreads B
and C was 34% at 5°C and 0% at 40°C.
The spread made without Myvacet LG K (comparative spread B) and the spread
made with the distilled monoglyceride, Myverol 18-04K (comparative spread C)
were both lacking smoothness and shine, when spread directly from the
refrigerator (5°C). They also had a somewhat uneven, crumbly and broken
appearance. The spread according to the invention made with Myvacet LG K
(Example 2) was however smooth, had a good plastic texture, and was shiny on
the surface. It is clear that Myvacet LG K provides particular advantages to
spreads made from oils which are non-hydrogenated and non-interesterified in
their natural form, for example palm oil, since it has surprisingly been found that a
margarine of superior appearance can be made even with non-hydrogenated non-
interesterified palm oil.
Claims (5)
1. A food product comprising: (a) from about 10% to 90% by weight of a fat phase comprising: (i) from about 95% to 99.9% by weight of the fat phase of a fat base having a solids profile characterised by a N5-value of from about 3 to 75, and a N40-value of from about 0 to15; and (ii) from about 0.1% to 5% by weight of the fat phase of a crystallisation modifying agent comprising at least one organic acid ester of mono- and diglycerides of fatty acids; and (b) from about 10% to 90% by weight of an aqueous phase; wherein the food product comprises no more than 3% by weight of trans unsaturated fatty acid residues based on the weight of the food product.
2. A food product as claimed in claim 1, wherein the fat phase is present in an amount of from about 20% to 80% by weight of the food product, preferably from about 30% to 70% by weight of the food product, more preferably from about 5% to 65% by weight of the food product, especially approximately 60% by weight of the food product.
3. A food product as claimed in claim 1 or claim 2, wherein the crystallisation modifying agent is present in the fat phase in an amount of from about 0.2% to 4% by weight of the fat phase, preferably from about 0.3% to 3% by weight of the fat phase, most preferably approximately 1.5% by weight of the fat phase.
4. A food product as claimed in any preceding claim, wherein the at least one organic acid ester of mono- and diglycerides of fatty acids of the crystallisation modifying agent is selected from: (i) acetic acid esters of mono- and diglycerides of fatty acids, also known as ACETEM (E 472a); (ii) lactic acid esters of mono- and diglycerides of fatty acids, also known as LACTEM (E 472b); (iii) citric acid esters of mono- and diglycerides of fatty acids, also known as CITREM (E 472C); and (iv) mono- and diacetyl tartaric acid esters of mono- and diglycerides of fatty acids, also known as DATEM (E 472e); (V) mixed acetic and tartaric acid esters of mono- and diglycerides of fatty acids, also known as MATEM (E 4720, and mixtures thereof; and wherein, preferably, the at least one organic acid ester of mono- and diglycerides of fatty acids is an acetic acid ester of mono- and diglycerides of fatty acids.
5. Use of an organic acid ester of mono- and diglycerides of fatty acids for improving the organoleptic properties of a food product as claimed in any one of claims 1 to 4.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
IEIRELAND20/10/2006S2006/0771 |
Publications (1)
Publication Number | Publication Date |
---|---|
IES85011Y1 true IES85011Y1 (en) | 2008-10-15 |
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