US3145110A - Shortening product - Google Patents
Shortening product Download PDFInfo
- Publication number
- US3145110A US3145110A US182843A US18284362A US3145110A US 3145110 A US3145110 A US 3145110A US 182843 A US182843 A US 182843A US 18284362 A US18284362 A US 18284362A US 3145110 A US3145110 A US 3145110A
- Authority
- US
- United States
- Prior art keywords
- shortening
- oil
- composition
- mix
- propylene glycol
- 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 - Lifetime
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- 238000004904 shortening Methods 0.000 title claims description 62
- 239000000203 mixture Substances 0.000 claims description 85
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 claims description 46
- 238000002156 mixing Methods 0.000 claims description 24
- 239000007787 solid Substances 0.000 claims description 18
- UFTFJSFQGQCHQW-UHFFFAOYSA-N triformin Chemical compound O=COCC(OC=O)COC=O UFTFJSFQGQCHQW-UHFFFAOYSA-N 0.000 claims description 13
- 239000012530 fluid Substances 0.000 claims description 12
- 239000007788 liquid Substances 0.000 claims description 10
- 150000004671 saturated fatty acids Chemical class 0.000 claims description 10
- 238000002360 preparation method Methods 0.000 claims description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 19
- 239000004615 ingredient Substances 0.000 description 19
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 18
- 239000000654 additive Substances 0.000 description 15
- 239000003921 oil Substances 0.000 description 11
- 235000019198 oils Nutrition 0.000 description 11
- 239000004033 plastic Substances 0.000 description 11
- 239000003549 soybean oil Substances 0.000 description 11
- 235000012424 soybean oil Nutrition 0.000 description 11
- 125000004432 carbon atom Chemical group C* 0.000 description 10
- 238000006243 chemical reaction Methods 0.000 description 10
- 235000011187 glycerol Nutrition 0.000 description 9
- 239000008173 hydrogenated soybean oil Substances 0.000 description 9
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 8
- 229910052740 iodine Inorganic materials 0.000 description 8
- 239000011630 iodine Substances 0.000 description 8
- 238000002844 melting Methods 0.000 description 8
- 230000008018 melting Effects 0.000 description 8
- 239000002199 base oil Substances 0.000 description 7
- FKOKUHFZNIUSLW-UHFFFAOYSA-N 2-Hydroxypropyl stearate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(C)O FKOKUHFZNIUSLW-UHFFFAOYSA-N 0.000 description 6
- IZHVBANLECCAGF-UHFFFAOYSA-N 2-hydroxy-3-(octadecanoyloxy)propyl octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(O)COC(=O)CCCCCCCCCCCCCCCCC IZHVBANLECCAGF-UHFFFAOYSA-N 0.000 description 6
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 6
- 239000007795 chemical reaction product Substances 0.000 description 6
- 235000014113 dietary fatty acids Nutrition 0.000 description 6
- 235000019197 fats Nutrition 0.000 description 6
- 239000000194 fatty acid Substances 0.000 description 6
- 229930195729 fatty acid Natural products 0.000 description 6
- 125000005456 glyceride group Chemical group 0.000 description 6
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 6
- 229910052753 mercury Inorganic materials 0.000 description 6
- 239000000047 product Substances 0.000 description 6
- 229940093625 propylene glycol monostearate Drugs 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- 230000008901 benefit Effects 0.000 description 5
- 239000013078 crystal Substances 0.000 description 5
- 235000013601 eggs Nutrition 0.000 description 5
- 150000002148 esters Chemical class 0.000 description 5
- 238000000034 method Methods 0.000 description 5
- 239000002994 raw material Substances 0.000 description 5
- VBICKXHEKHSIBG-UHFFFAOYSA-N 1-monostearoylglycerol Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(O)CO VBICKXHEKHSIBG-UHFFFAOYSA-N 0.000 description 4
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 4
- 235000021355 Stearic acid Nutrition 0.000 description 4
- 150000004665 fatty acids Chemical class 0.000 description 4
- 235000013336 milk Nutrition 0.000 description 4
- 239000008267 milk Substances 0.000 description 4
- 210000004080 milk Anatomy 0.000 description 4
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 4
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 4
- 239000008117 stearic acid Substances 0.000 description 4
- 230000000996 additive effect Effects 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- 235000012343 cottonseed oil Nutrition 0.000 description 3
- 239000002385 cottonseed oil Substances 0.000 description 3
- 239000003995 emulsifying agent Substances 0.000 description 3
- 235000013861 fat-free Nutrition 0.000 description 3
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 3
- -1 lard Substances 0.000 description 3
- 230000035515 penetration Effects 0.000 description 3
- 238000007790 scraping Methods 0.000 description 3
- 150000003626 triacylglycerols Chemical class 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 235000019484 Rapeseed oil Nutrition 0.000 description 2
- 244000299461 Theobroma cacao Species 0.000 description 2
- LUTSRLYCMSCGCS-BWOMAWGNSA-N [(3s,8r,9s,10r,13s)-10,13-dimethyl-17-oxo-1,2,3,4,7,8,9,11,12,16-decahydrocyclopenta[a]phenanthren-3-yl] acetate Chemical compound C([C@@H]12)C[C@]3(C)C(=O)CC=C3[C@@H]1CC=C1[C@]2(C)CC[C@H](OC(=O)C)C1 LUTSRLYCMSCGCS-BWOMAWGNSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 238000013019 agitation Methods 0.000 description 2
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 2
- 235000008429 bread Nutrition 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 239000000796 flavoring agent Substances 0.000 description 2
- 235000019634 flavors Nutrition 0.000 description 2
- 235000013312 flour Nutrition 0.000 description 2
- YQEMORVAKMFKLG-UHFFFAOYSA-N glycerine monostearate Natural products CCCCCCCCCCCCCCCCCC(=O)OC(CO)CO YQEMORVAKMFKLG-UHFFFAOYSA-N 0.000 description 2
- SVUQHVRAGMNPLW-UHFFFAOYSA-N glycerol monostearate Natural products CCCCCCCCCCCCCCCCC(=O)OCC(O)CO SVUQHVRAGMNPLW-UHFFFAOYSA-N 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 238000010348 incorporation Methods 0.000 description 2
- 238000009884 interesterification Methods 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 239000003381 stabilizer Substances 0.000 description 2
- 239000003760 tallow Substances 0.000 description 2
- DCXXMTOCNZCJGO-UHFFFAOYSA-N tristearoylglycerol Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(OC(=O)CCCCCCCCCCCCCCCCC)COC(=O)CCCCCCCCCCCCCCCCC DCXXMTOCNZCJGO-UHFFFAOYSA-N 0.000 description 2
- 235000015112 vegetable and seed oil Nutrition 0.000 description 2
- JNYAEWCLZODPBN-JGWLITMVSA-N (2r,3r,4s)-2-[(1r)-1,2-dihydroxyethyl]oxolane-3,4-diol Chemical compound OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O JNYAEWCLZODPBN-JGWLITMVSA-N 0.000 description 1
- 239000004385 Aspartame-acesulfame salt Substances 0.000 description 1
- 239000004255 Butylated hydroxyanisole Substances 0.000 description 1
- 239000004322 Butylated hydroxytoluene Substances 0.000 description 1
- NLZUEZXRPGMBCV-UHFFFAOYSA-N Butylhydroxytoluene Chemical compound CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 NLZUEZXRPGMBCV-UHFFFAOYSA-N 0.000 description 1
- 241000252203 Clupea harengus Species 0.000 description 1
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 1
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- 235000019482 Palm oil Nutrition 0.000 description 1
- 235000019483 Peanut oil Nutrition 0.000 description 1
- 229920001214 Polysorbate 60 Polymers 0.000 description 1
- 240000004808 Saccharomyces cerevisiae Species 0.000 description 1
- 235000003434 Sesamum indicum Nutrition 0.000 description 1
- 244000000231 Sesamum indicum Species 0.000 description 1
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 1
- 241000529895 Stercorarius Species 0.000 description 1
- CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 description 1
- 229930006000 Sucrose Natural products 0.000 description 1
- 235000009470 Theobroma cacao Nutrition 0.000 description 1
- 238000002441 X-ray diffraction Methods 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 235000019282 butylated hydroxyanisole Nutrition 0.000 description 1
- CZBZUDVBLSSABA-UHFFFAOYSA-N butylated hydroxyanisole Chemical compound COC1=CC=C(O)C(C(C)(C)C)=C1.COC1=CC=C(O)C=C1C(C)(C)C CZBZUDVBLSSABA-UHFFFAOYSA-N 0.000 description 1
- 229940043253 butylated hydroxyanisole Drugs 0.000 description 1
- 235000010354 butylated hydroxytoluene Nutrition 0.000 description 1
- 229940095259 butylated hydroxytoluene Drugs 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 235000019219 chocolate Nutrition 0.000 description 1
- 229960004106 citric acid Drugs 0.000 description 1
- 235000015165 citric acid Nutrition 0.000 description 1
- 239000003240 coconut oil Substances 0.000 description 1
- 235000019864 coconut oil Nutrition 0.000 description 1
- 239000013065 commercial product Substances 0.000 description 1
- 235000009508 confectionery Nutrition 0.000 description 1
- 235000005687 corn oil Nutrition 0.000 description 1
- 239000002285 corn oil Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 235000014103 egg white Nutrition 0.000 description 1
- 210000000969 egg white Anatomy 0.000 description 1
- 238000005485 electric heating Methods 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 238000001640 fractional crystallisation Methods 0.000 description 1
- 235000021588 free fatty acids Nutrition 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 239000004519 grease Substances 0.000 description 1
- 235000019514 herring Nutrition 0.000 description 1
- 238000005984 hydrogenation reaction Methods 0.000 description 1
- 229910052816 inorganic phosphate Inorganic materials 0.000 description 1
- 229910017053 inorganic salt Inorganic materials 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 238000010899 nucleation Methods 0.000 description 1
- 239000004006 olive oil Substances 0.000 description 1
- 235000008390 olive oil Nutrition 0.000 description 1
- 238000012856 packing Methods 0.000 description 1
- 239000003346 palm kernel oil Substances 0.000 description 1
- 235000019865 palm kernel oil Nutrition 0.000 description 1
- 239000002540 palm oil Substances 0.000 description 1
- 239000000312 peanut oil Substances 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 235000003441 saturated fatty acids Nutrition 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- 239000005720 sucrose Substances 0.000 description 1
- 235000020238 sunflower seed Nutrition 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 238000005496 tempering Methods 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 238000010792 warming Methods 0.000 description 1
- 239000010698 whale oil Substances 0.000 description 1
Images
Classifications
-
- A—HUMAN NECESSITIES
- A21—BAKING; EDIBLE DOUGHS
- A21D—TREATMENT OF FLOUR OR DOUGH FOR BAKING, e.g. BY ADDITION OF MATERIALS; BAKING; BAKERY PRODUCTS
- A21D2/00—Treatment of flour or dough by adding materials thereto before or during baking
- A21D2/08—Treatment of flour or dough by adding materials thereto before or during baking by adding organic substances
- A21D2/14—Organic oxygen compounds
- A21D2/16—Fatty acid esters
- A21D2/165—Triglycerides
-
- A—HUMAN NECESSITIES
- A21—BAKING; EDIBLE DOUGHS
- A21D—TREATMENT OF FLOUR OR DOUGH FOR BAKING, e.g. BY ADDITION OF MATERIALS; BAKING; BAKERY PRODUCTS
- A21D2/00—Treatment of flour or dough by adding materials thereto before or during baking
- A21D2/08—Treatment of flour or dough by adding materials thereto before or during baking by adding organic substances
- A21D2/14—Organic oxygen compounds
- A21D2/145—Acids, anhydrides or salts thereof
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23D—EDIBLE OILS OR FATS, e.g. MARGARINES, SHORTENINGS OR COOKING OILS
- A23D9/00—Other edible oils or fats, e.g. shortenings or cooking oils
- A23D9/007—Other edible oils or fats, e.g. shortenings or cooking oils characterised by ingredients other than fatty acid triglycerides
- A23D9/013—Other fatty acid esters, e.g. phosphatides
Definitions
- This invention relates to neW and improved shortening compositions. More particularly, it relates to a fluid shortening composition which is capable of producing more tender cakes, With a variety of recipes, under commercial conditions, than is possible with a conventional plastic shortening, with the additional feature that the cakes can be prepared With a single mixing step.
- a further object of this invention is to provide a fluid shortening product which gives more tender cakes than conventional plastic shortenings.
- a still further object of this invention is to provide a fluid shortening composition which is capable of producing acceptable cakes With only a single mixing step.
- the accompanying drawing shows a highly simplified flow chart of a process for making a preferred form of additive.
- the fluid shortening compositions of this invention comprise a normally liquid triglyceride oil containing as additives from about 0.5% to about 8% of the monoester of propylene glycol and a saturated fatty acid having from 14 to 22 carbon atoms; from about 1% to about normally solid triglyceride fat; and from about 0.5% to about 10% saturated fatty acid having from 14 to 22 carbon atoms. All percentages mentioned herein are by total Weight of the shortening composition.
- the fluid shortening compositions of this invention have several advantages. First, cakes made with these shortening compositions are more tender and moist than cakes made With plastic shortenings. Second, the cakes have essentially equal or slightly greater volume than cakes made With plastic shortenings. Third, the cakes can be prepared With only a single mixing step. Fourth, the shortening compositions can be used with a wide variety of recipes and mixing procedures. Fifth, the shortening maintains satisfactory fluidity characteristics and homogeneity for extended storage periods.
- the normally liquid triglyceride base oil should have satisfactory keeping quality and, preferably, only a minimum amount of solids at the expected temperatures to Which the shortening Will be exposed.
- Suitable base oils for this invention can be derived from animal, Vegetable,
- liquid triglyceride oils such as cottonseed oil, soybean oil, rapeseed oil, sesame seed oil, and sunflower seed oil.
- suitable liquid oil fractions can be obtained from palm oil, lard, and tallow, as for example, by fractional crystallization or directed interesterification, followed by separation of the oil.
- Oils predominating in glycerides of unsaturated acids may require some hydrogenation to main tain flavor, but care should be taken not to greatly increase the amount of glycerides melting about 60 F. When the oil has too many solids melting between 60 F. and 100 F, it may be necessary to separate out these solids.
- Refined cottonseed oil and refined and slightly hydrogenated soybean oil (Iodine Value of about llOilO) have proved very satisfactory for use as glyceride base oils of this invention.
- the percentage limits of the additives of this invention are determined by various considerations. There should be from about 0.5% to about 8% propylene glycol monoester of a saturated fatty acid having from 14 to 22 carbon atoms dissolved in the normally liquid glyceride oil. This additive aids in the incorporation of air during the mixing step.
- propylene glycol monoester of a saturated fatty acid having from 14 to 22 carbon atoms dissolved in the normally liquid glyceride oil. This additive aids in the incorporation of air during the mixing step.
- For single-stage mixing in which all the batter ingredients are added to the mixing container at one time, there should be present in the shortening composition at least about 1.5% propylene glycol monoester. This amount is needed only if all kinds of cakes are to be prepared, since some cake batters can be mixed single-stage with only about 0.5% propylene glycol monoester in the shortening.
- the shortening composition there should be present in the shortening composition from about 1% to about 5% normally solid triglyceride fat which is ordinarily a substantially completely hydrogenated triglyceride oil. It is also desirable, but not H essential, to include in the shortening about 0.05% to about 5% of partial ester of glycerine and substantially saturated fatty acid. These two additives can be either pure esters of fatty acids having from 14 to 22 carbon atoms, or mixtures of fatty acid esters containing such fatty acids. The upper limits are set by the viscosity, stability, and consistency requirements of the product.
- the shortening composition there should also be present in the shortening composition at least /2% saturated free fatty acid having from 14 to 22 carbon atoms.
- This additive not only improves the effectiveness of the propylene glycol monoester and mono or diglyceride emulsifiers in increasing the air incorporation during the mixing step, but also acts as a high temperature batter stabilizer which prevents loss of air during the baking step and shrinkage during and subsequent to baking of the cake.
- this high temperature batter stabilizer and the propylene glycol monoester has been found to be necessary to achieve the single-stage mixing advantages of this invention.
- the total percentage of monoester of propylene glycol, partial ester of glycerine and fatty acid in the shortening composition preferably should not exceed about 14%.
- the solid triglyceride and the partial glycerides should be at least in beta phase, as opposed to alpha and beta-prime phases.
- These types of crystalline structure can be identified by their X-ray diffraction patterns and are described in detail in US. Patents 2,521,242 and 2,521,243, issued September 5, 1950.
- a preferred embodiment of the fluid shortening composition of this invention comprises soybean oil hydrogenated to an Iodine Value of from 100 to 120 and having therein, as additives, from about 3% to about propylene glycol monostearate, from about 1% to about 3% substantially completely hydrogenated soybean oil, from about 3% to about 4% monoand diglycerides of saturated fatty acids having from 14 to 22 carbon atoms, and from about 0.6% to about 2% stearic acid.
- antioxidants including butylated hydroxytoluene, butylated hydroxyanisole, citric acid, and methyl silicone can also be added to the shortening composition if desired.
- the shortening composition can be processed according to the teaching of US. Patent 2,815,286, granted to Andre and- Going December 3, 1957.
- the main steps can include heating the shortening composition to a high enough temperature to melt all the solids, rapidly chilling to form small crystals and then warming to between 90 F. and 100 F. to promote a change of the solid triglyceride fat from alpha and bcta-prime phases to beta-phase either with or Without seeding with beta-phase crystals.
- An alternative method is to warm the rapidly chilled mixture to a temperature above the melting point of the alpha and beta-prime phases but below the melting point of the beta phase crystals and then cooling the mixture using the beta phase crystals already present as seed crystals.
- An added tempering step for the shortenings of this invention of one to two days at 80 F. to 90 F., after packing, is desirable. This processing results in forming a stable suspension of the undissolved additives in the base oil.
- the shortening compositions of this invention in addition to being exceptionally good for baking all kinds of cakes, are also good for pie doughs, bread, flat icings, and sweet yeast breads.
- the bulk of the additives can be prepared in a convenient single process by reacting substantially completely hydrogenated triglycerides and propylene glycol in the presence of an interesterification catalyst at elevated temperatures.
- Suitable equipment for preparing the additives can consist of a reaction vessel equipped with means for heating and cooling, means for agitating the contents of the vessel, means for removing excess glycerine and glycol and a condenser attached to a vapor line coming from the vessel.
- a condensate receiver can be attached to said condenser and raw'material handling tanks and lines; a settling tank; and a means for filtering can be added to the apparatus, if desired.
- Reference numeral 5 represents generally a pressure resistant reaction vessel.
- raw material inlet pipes are represented generally by 7).
- the mixture was then agitated for about Vi hour, and then about 6.2 of 85% H PO was added through inlet 7.
- the mixture was agitated for another /2 hour, and for the last approximately 15 minutes the pressure was reduced to about inch of mercury absolute.
- the mixture was then cooled to about 170 F, and dropped by gravity to a settling tank 25 through the line 23 where the inorganic phosphate salts were allowed to settle out of the stock for about one hour, and the mixture was then filtered through double filter paper in a filter press 27.
- Any triglyceride source can be used other than soybean oil so long as it contains a major portion of saturated fatty acid radicals having from 14 to 22 carbon atoms.
- examples of such sources include tallow, rapeseed oil, cottonseed oil, palm kernel oil, herring oil, peanut oil, corn oil, olive oil, whale oil, and coconut oil which have been hydrogenated.
- Example 1 The product of Example 1 was analyzed and it was found to consist'of the following approximate percentages of components.
- the figures given as total percent of tristearin-propylene glycol distearin, and distearin also include 16.2% free stearic acid.
- the glycerol monostearate is about 90% glycerol l-monostearate and the distearin is about 90% 1,3 distearin.
- Yellow Cake Ingredients Instructions (All mixing is at slow speed) Mix these ingredients for 90 seconds ggg 'gfii, scrape down, mix an additional 90 g e g seconds, and then scrape down again.
- Yellow Pound Cake Ingredients I Instructions 454 gm. flour 318 Shortening additional 90 seconds, and then scrape down.
- Chocolate Fudge Cake Ingredients Instructions Mix these ingredients for 3 to 5 minutes, 482 gm. flour.--.. scraping down at least once. All
- mixing is at slow speed in a three-speed 400 gm. shortening mixer, or at the second slowest speed in a four-speed mixer.
- Pene- Exarnple Cake tration Batter number Shortening Type of cake volume, 0.1 density, cc./lb. mm./5 gm./cc. secs.
- the penetration was generally greater for the cakes made with the shortening composition of this invention. This indicates that these cakes were more tender than the cakes made with conventional plastic shortenings.
- the cakes were of comparable size and it was more convenient to measure the shortening and mix the ingredients with a pourable shortening composition.
- EXAMPLE 16 A mixture of additives was prepared by generally the same reactions as in Example 1, but under somewhat dif-( ferent conditions of temperature and pressure. 92.5 parts of refined and bleached soybean oil hydrogenated to an Iodine Value of about 8 was heated to about 250 F. at an absolute pressure of 25 inches of mercury in a reaction vessel and 46.2 parts of propylene glycol and 1.39 parts of 50% NaOH were added. The temperature was increased to 350 F, the pressure was increased to 15 pounds per square inch in an atmosphere of nitrogen, and the mixture was mechanically agitated while the reaction continned for one hour. The mixture was cooled to about 200 F. and the NaOH was neutralized with 2.16 parts of phosphoric acid while the mixture was agitated for a half hour. The mixture was then heated to 250 F. and a full vacuum was produced in the reaction vessel to remove the free propylene glycol and glycerine. This alas,
- Shortenings which will give results equivalent to the shortenings prepared with the reaction product of Example 1 can be prepared with this reaction product. In general, less of this product is required to give the same level of propylene glycol monostearate than the shortenings made from the reaction product of Example 1.
- Table III contains data relating to white cakes prepared With both regular and single-stage mixing.
- the shortenings contain as a base oil, hydrogenated, refined, bleached, and deodorized soybean oil (Iodine Value of 107) containing 2.3%, by weight of this base oil, of soybean oil hydrogenated to an Iodine Value of 8. 92% of this mixture of hydrogenated soybean oils was processed with 8% of the reaction product of Example 1 to give a shortening, hereinafter referred to as Invention and 92% of the mixture of hydrogenated soybean oils was mixed with 8% of the reaction product of Example 16 to give a shortening, hereinafter referred to as Invention? TABLE III Penetration, 0.1 nun/ sees.
- a stable fluid shortening composition suitable for use in the preparation of recipe cake batters with a single mixing step in large scale commercial baking operations, which Comprises a n rma qui elvesid Q l h in therein from about 0.5% to about 8% by weight of the composition, of mono-ester of propylene glycol and saturated fatty acid containing from 14 to 22 carbon atoms, said shortening composition additionally comprising, by weight of the composition, from about 1% to about 5% normally solid triglyceride fat and from about 0.5% to about 10%of saturated fatty acid having from 14 to 22 carbon atoms, said triglyceride fat being at least in beta phase.
- composition of claim 1 in which the normally liquid glyceride oil is soybean oil with an Iodine Value of from about to about 120, the monoester of propylene glycol is monostearate, the normally solid triglyceride fat is substantially completely hydrogenated soybean oil and the fatty acid is stearic acid.
- a stable fluid shortening composition suitable for use in the preparation of recipe cake batters with a single mixing step in large scale commercial baking operations, which comprises soybean oil hydrogenated to an Iodine Value of from about 100 to about having therein from about 3% to 5%, by weight of the composition of propylene glycol monostearate, said shortening composition additionally comprising, by weight of the composition, from about 1% to about 3% substantially completely hydrogenated soybean oil, from about 3% to about 4% normally solid partial ester of glycerine and substantially saturated fatty acid having from 14 to 22 carbon atoms, and from about 0.6% to about 2% of stearic acid, said substantially completely hydrogenated soybean oil and said partial ester of glycerine being at least 80% in beta phase, said shortening being substantially free from intermediate melting solids.
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- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Food Science & Technology (AREA)
- Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Polymers & Plastics (AREA)
- Bakery Products And Manufacturing Methods Therefor (AREA)
Description
Aug. 18, 1964 c, T. ABBOTT, JR
SHORTENING PRODUCT Filed March 27, 1962 (WM em fa/zde/gsafe 4 726660497 EY/er INVENTOR Cfiarles fieaior'z'k' N" ATTORNEY United States Patent Office 3,l45,ll Patented Aug. 13, 1964 3,145,110 SIl-TQRTENHNG PRQDTJQT Charles Theodoric Abbott, .lzn, tCincinnati, @hio, assignor to The Procter dz Gamble @ompany, (Iincinnati, Ohio, a corporation of fiflhio Filed 27, E962, Ser. No. 182,343 3 Claims. (tCl. 923 123) This invention relates to neW and improved shortening compositions. More particularly, it relates to a fluid shortening composition which is capable of producing more tender cakes, With a variety of recipes, under commercial conditions, than is possible with a conventional plastic shortening, with the additional feature that the cakes can be prepared With a single mixing step.
This application is a continuation-impart of application Serial No. 107,822, filed May 4, 1961, now abandoned.
Conventional commercial baking practice has been to use a plastic shortening for baking cakes. This practice has been necessary since all of the Wide variety of cakes that a commercial bakery prepares cannot be made with conventional liquid shortenings. However, fluid shortenings have a definite advantage in handling and storage, and a fluid product Which would perform satisfactorily would be extremely useful.
Accordingly, it is an object of this invention to provide a liquid shortening composition which can be used in baking a Wide variety of cakes.
A further object of this invention is to provide a fluid shortening product which gives more tender cakes than conventional plastic shortenings.
A still further object of this invention is to provide a fluid shortening composition which is capable of producing acceptable cakes With only a single mixing step. Other objects and advantageous features Will be evident from the following detailed description of the invention.
The accompanying drawing shows a highly simplified flow chart of a process for making a preferred form of additive.
In general, the fluid shortening compositions of this invention comprise a normally liquid triglyceride oil containing as additives from about 0.5% to about 8% of the monoester of propylene glycol and a saturated fatty acid having from 14 to 22 carbon atoms; from about 1% to about normally solid triglyceride fat; and from about 0.5% to about 10% saturated fatty acid having from 14 to 22 carbon atoms. All percentages mentioned herein are by total Weight of the shortening composition.
The fluid shortening compositions of this invention have several advantages. First, cakes made with these shortening compositions are more tender and moist than cakes made With plastic shortenings. Second, the cakes have essentially equal or slightly greater volume than cakes made With plastic shortenings. Third, the cakes can be prepared With only a single mixing step. Fourth, the shortening compositions can be used with a wide variety of recipes and mixing procedures. Fifth, the shortening maintains satisfactory fluidity characteristics and homogeneity for extended storage periods.
The normally liquid triglyceride base oil should have satisfactory keeping quality and, preferably, only a minimum amount of solids at the expected temperatures to Which the shortening Will be exposed. Suitable base oils for this invention can be derived from animal, Vegetable,
or marine sources including naturally-occurring liquid triglyceride oils such as cottonseed oil, soybean oil, rapeseed oil, sesame seed oil, and sunflower seed oil. Also, suitable liquid oil fractions can be obtained from palm oil, lard, and tallow, as for example, by fractional crystallization or directed interesterification, followed by separation of the oil. Oils predominating in glycerides of unsaturated acids may require some hydrogenation to main tain flavor, but care should be taken not to greatly increase the amount of glycerides melting about 60 F. When the oil has too many solids melting between 60 F. and 100 F, it may be necessary to separate out these solids. Refined cottonseed oil and refined and slightly hydrogenated soybean oil (Iodine Value of about llOilO) have proved very satisfactory for use as glyceride base oils of this invention.
The percentage limits of the additives of this invention are determined by various considerations. There should be from about 0.5% to about 8% propylene glycol monoester of a saturated fatty acid having from 14 to 22 carbon atoms dissolved in the normally liquid glyceride oil. This additive aids in the incorporation of air during the mixing step. For single-stage mixing, in which all the batter ingredients are added to the mixing container at one time, there should be present in the shortening composition at least about 1.5% propylene glycol monoester. This amount is needed only if all kinds of cakes are to be prepared, since some cake batters can be mixed single-stage with only about 0.5% propylene glycol monoester in the shortening.
There should be present in the shortening composition from about 1% to about 5% normally solid triglyceride fat which is ordinarily a substantially completely hydrogenated triglyceride oil. It is also desirable, but not H essential, to include in the shortening about 0.05% to about 5% of partial ester of glycerine and substantially saturated fatty acid. These two additives can be either pure esters of fatty acids having from 14 to 22 carbon atoms, or mixtures of fatty acid esters containing such fatty acids. The upper limits are set by the viscosity, stability, and consistency requirements of the product.
There should also be present in the shortening composition at least /2% saturated free fatty acid having from 14 to 22 carbon atoms. This additive not only improves the effectiveness of the propylene glycol monoester and mono or diglyceride emulsifiers in increasing the air incorporation during the mixing step, but also acts as a high temperature batter stabilizer which prevents loss of air during the baking step and shrinkage during and subsequent to baking of the cake. Moreover, the combined presence of this high temperature batter stabilizer and the propylene glycol monoester has been found to be necessary to achieve the single-stage mixing advantages of this invention.
The total percentage of monoester of propylene glycol, partial ester of glycerine and fatty acid in the shortening composition preferably should not exceed about 14%.
The solid triglyceride and the partial glycerides should be at least in beta phase, as opposed to alpha and beta-prime phases. These types of crystalline structure can be identified by their X-ray diffraction patterns and are described in detail in US. Patents 2,521,242 and 2,521,243, issued September 5, 1950.
It is desirable, though unnecessary for the single-stage mixing properties of this invention, to form the shortening composition so that it is substantially free from intermediate melting solids (i.e., melting between 60 F. and 100 F.) which would cause consistency problems as a result of their melting and resolidification due to normal changes in temperature.
A preferred embodiment of the fluid shortening composition of this invention comprises soybean oil hydrogenated to an Iodine Value of from 100 to 120 and having therein, as additives, from about 3% to about propylene glycol monostearate, from about 1% to about 3% substantially completely hydrogenated soybean oil, from about 3% to about 4% monoand diglycerides of saturated fatty acids having from 14 to 22 carbon atoms, and from about 0.6% to about 2% stearic acid.
When the additives of this invention are used in a shortening, the presence of other additives such as the partial fatty acid esters of sucrose, sorbitol, sorbitan, polyoxyethylene sorbitan and the like is not precluded, since conventional benefits may still be derived by their use. It will be recognized, of course, that the presence of other additives may have an effect on the operation of the additives of this invention and, therefore, the desirability of their use will depend upon the results desired.
Various minor ingredients such as antioxidants, including butylated hydroxytoluene, butylated hydroxyanisole, citric acid, and methyl silicone can also be added to the shortening composition if desired.
The shortening composition can be processed according to the teaching of US. Patent 2,815,286, granted to Andre and- Going December 3, 1957. The main steps can include heating the shortening composition to a high enough temperature to melt all the solids, rapidly chilling to form small crystals and then warming to between 90 F. and 100 F. to promote a change of the solid triglyceride fat from alpha and bcta-prime phases to beta-phase either with or Without seeding with beta-phase crystals. An alternative methodis to warm the rapidly chilled mixture to a temperature above the melting point of the alpha and beta-prime phases but below the melting point of the beta phase crystals and then cooling the mixture using the beta phase crystals already present as seed crystals. An added tempering step for the shortenings of this invention of one to two days at 80 F. to 90 F., after packing, is desirable. This processing results in forming a stable suspension of the undissolved additives in the base oil.
The shortening compositions of this invention, in addition to being exceptionally good for baking all kinds of cakes, are also good for pie doughs, bread, flat icings, and sweet yeast breads.
The bulk of the additives can be prepared in a convenient single process by reacting substantially completely hydrogenated triglycerides and propylene glycol in the presence of an interesterification catalyst at elevated temperatures. Suitable equipment for preparing the additives can consist of a reaction vessel equipped with means for heating and cooling, means for agitating the contents of the vessel, means for removing excess glycerine and glycol and a condenser attached to a vapor line coming from the vessel. A condensate receiver can be attached to said condenser and raw'material handling tanks and lines; a settling tank; and a means for filtering can be added to the apparatus, if desired.
It is believed that the invention will be better understood from the following example described in connection with the drawing, FIGURE 1, but is not limited to the specific process set forth therein.
EXAMPLE 1 Reference numeral 5 represents generally a pressure resistant reaction vessel.
Approximately 95.6 parts of completely hydrogenated triglycerides derived from soybean oil, were introduced to the reaction vessel 5 through a raw material inlet pipe (raw material inlet pipes are represented generally by 7).
Any triglyceride source can be used other than soybean oil so long as it contains a major portion of saturated fatty acid radicals having from 14 to 22 carbon atoms. Examples of such sources include tallow, rapeseed oil, cottonseed oil, palm kernel oil, herring oil, peanut oil, corn oil, olive oil, whale oil, and coconut oil which have been hydrogenated.
The product of Example 1 was analyzed and it was found to consist'of the following approximate percentages of components.
Glycerol monostearate 2.7
Propylene glycol monostearate 27.3
Distearin 5.6
Tristearin Propylene glycol distearin Glycerin 0.9
Glycol 0.2
The figures given as total percent of tristearin-propylene glycol distearin, and distearin also include 16.2% free stearic acid. The glycerol monostearate is about 90% glycerol l-monostearate and the distearin is about 90% 1,3 distearin.
About 6% to 12%, preferably 8% (and in no event less than about 2%), of the emulsifier system prepared by the process hereinbefore described and about 2% to 4% completely hydrogenated soybean oil, preferably 2%, are added to a base oil and give a highly improved liquid shortening composition having the capability of being used in single-stage mixing.
The following examples are illustrative of the superior results that can be achieved with the shortening compositions of this invention.
In the following examples, four cakes were used. The recipes for these cakes are as follows:
White Cake scrape down, and then mix [or an additional 90 seconds.
Add approximately of these ingredients and mix for 45 seconds, then scrape down. Mix an additional 45 seconds, add the rest of the ingredients, mix 45 seconds, scrape down and then mix for 45 more seconds.
54 gm. non-fat milk solids-.-.
178 gm. water 341 gm. egg whites Place 400 gm. of the batter in 8-inch pans and bake at 375 F. for 20 minutes.
Yellow Cake Ingredients Instructions (All mixing is at slow speed) Mix these ingredients for 90 seconds ggg 'gfii, scrape down, mix an additional 90 g e g seconds, and then scrape down again.
636 gm. sugar 17 gm. salt Add these ingredients ,mix for 90 seconds, 28 gm. baking powder scrape down and then mix for an addi- 200 gm, water tional 90 seconds.
60 gm. non-fat milk solids..-.
Add approximately of these ingredients, mix 45 seconds, scrape down, mix 45 more seconds, add the rest of the ingredients, mix 45 seconds, scrape down, and then mix for an additional 45 seconds.
217 gm. water 272 gm. whole eggs Place 400 gm. of the batter into an S'inch pan and bake at 375 F. for 23 minutes.
Yellow Pound Cake Ingredients I Instructions 454 gm. flour 318 Shortening additional 90 seconds, and then scrape down.
Add these ingredients, mix 180 seconds at second speed, scrape down, and then mix an additional 180 seconds.
Add approximately of these eggs in 70 seconds while mixing at slow speed, mix for 40 seconds, add the rest of the eggs in 70 seconds while mixing at slow speed, scrape down, and then mix for an additional 120 seconds.
{Mix these ingredients for 90 seconds at 17 gm. sali;.. 200 gm. water 27 gm. nonfat milk solids....
545 gm. sugar 318 gm. whole eggs Place 454- gm. of the batter in a standard loaf pan and bake at 360 F. for 55 minutes.
Chocolate Fudge Cake Ingredients Instructions Mix these ingredients for 3 to 5 minutes, 482 gm. flour.--.. scraping down at least once. All
85 gm. cocoa...
mixing is at slow speed in a three-speed 400 gm. shortening mixer, or at the second slowest speed in a four-speed mixer.
710 gm. sugar 21 gm. salt.... gm. soda 21 gm. baking powder" 22'1 gm. water 50 gm. non-lat milk solids.-..
. Add these ingredients and mix for 3 to 5 minutes, scraping down at least once.
Add approximately of these ingredients, mix until smooth, scrape down, mix until smooth again, add the rest of the ingredients, and mix for an additional 3 to 5 minutes, scraping down to insure a smooth hatter.
510 gm. whole eggs 743 gm. water Flavor to taste Place 400 gm. of the batter in an 8-inch pan and bake at 360 F. for minutes.
second soeed, scrape down, mix an Ii TABLE I Cakes made with a standard plastic shortening derived from vegetable oil, referred to in the following table as plastic, were compared with a refined, bleached, and deodorized soybean oil (hydrogenated to an Iodine Value of 107) containing 8% commercial grade propylene glycol monostearate (50% monoester), 4% substantially completely hydrogenated (i.e., solid) monoand diglyccride or" soybean oil, 1% stcaric acid, and 2% snbstantially completely hydrogenated soybean oil, referred to in the following table as Invention. Penetration values were obtained by placing a standard grease cone on the cake and measuring the number of tenths of a millimeter the cone penetrated the cake in five seconds.
Pene- Exarnple Cake tration, Batter number Shortening Type of cake volume, 0.1 density, cc./lb. mm./5 gm./cc. secs.
Plastic. 1, 250 219 1.02 Invention. l, 195 223 96 Plastic. 1, 515 229 1. 00 Invention. 1, 635 262 93 Plastic.. 1,135 170 Invention- 1, 055 182 .87
As can be seen, the penetration was generally greater for the cakes made with the shortening composition of this invention. This indicates that these cakes were more tender than the cakes made with conventional plastic shortenings. The cakes were of comparable size and it was more convenient to measure the shortening and mix the ingredients with a pourable shortening composition.
TABLE II This table demonstrates the effectiveness of the instant invention in permitting single-stage batter mixing. The shortening was the fluid shortening composition of Table I. The recipes were altered in that all the ingredients were mixed together at once in single-stage mixing.
Pene- Example Cake tration, Batter No. Type of mixing Type of cake volume, 0.1 density ce./lb. mm./5
secs.
8 Regular 243 0. 99 9 Single stage. 230 .90 10 Regular 255 97 Single stage... 276 .87 Regular 191 88 Single stage. 210 77 Regular 272 .93 Single stage. 338 73 As can easily be seen, the shortening composition gives comparable results with single-stage mixing for a wide variety of cakes. This is a distinct advantage in a commercial product where simplicity leads directly to savings in time and cost.
EXAMPLE 16 A mixture of additives was prepared by generally the same reactions as in Example 1, but under somewhat dif-( ferent conditions of temperature and pressure. 92.5 parts of refined and bleached soybean oil hydrogenated to an Iodine Value of about 8 was heated to about 250 F. at an absolute pressure of 25 inches of mercury in a reaction vessel and 46.2 parts of propylene glycol and 1.39 parts of 50% NaOH were added. The temperature was increased to 350 F, the pressure was increased to 15 pounds per square inch in an atmosphere of nitrogen, and the mixture was mechanically agitated while the reaction continned for one hour. The mixture was cooled to about 200 F. and the NaOH was neutralized with 2.16 parts of phosphoric acid while the mixture was agitated for a half hour. The mixture was then heated to 250 F. and a full vacuum was produced in the reaction vessel to remove the free propylene glycol and glycerine. This alas,
removal was continued for one and a half hours. The absolute pressure was then raised to 25 inches of mercury, the mixture was cooled to 200 F, 4.53 parts of 50% NaOH was added, and the mixture was agitated for a half hour. The NaOH was then neutralized with 6.66 parts 85% phosphoric acid, and the mixture was agitated for another half hour. A'full vacuum was produced in the reaction vessel, the mixture was cooled to 100 F., and allowed to drain to a settling tank. After the inorganic salt had settled, they were filtered. This reaction mixture had a higher percentage of propylene glycol monostearate than the reaction product in Example 1.
Shortenings which will give results equivalent to the shortenings prepared with the reaction product of Example 1 can be prepared with this reaction product. In general, less of this product is required to give the same level of propylene glycol monostearate than the shortenings made from the reaction product of Example 1.
Table III contains data relating to white cakes prepared With both regular and single-stage mixing. The shortenings contain as a base oil, hydrogenated, refined, bleached, and deodorized soybean oil (Iodine Value of 107) containing 2.3%, by weight of this base oil, of soybean oil hydrogenated to an Iodine Value of 8. 92% of this mixture of hydrogenated soybean oils was processed with 8% of the reaction product of Example 1 to give a shortening, hereinafter referred to as Invention and 92% of the mixture of hydrogenated soybean oils was mixed with 8% of the reaction product of Example 16 to give a shortening, hereinafter referred to as Invention? TABLE III Penetration, 0.1 nun/ sees.
Example Type of mixing Cc./lb.
number Type of shortening Invention Invention Invention Invention Single stage $3 any way by these examples which are merely illustrative of the results obtainable with this invention.
What is claimed is:
l. A stable fluid shortening composition, suitable for use in the preparation of recipe cake batters with a single mixing step in large scale commercial baking operations, which Comprises a n rma qui elvesid Q l h in therein from about 0.5% to about 8% by weight of the composition, of mono-ester of propylene glycol and saturated fatty acid containing from 14 to 22 carbon atoms, said shortening composition additionally comprising, by weight of the composition, from about 1% to about 5% normally solid triglyceride fat and from about 0.5% to about 10%of saturated fatty acid having from 14 to 22 carbon atoms, said triglyceride fat being at least in beta phase.
2. The composition of claim 1 in which the normally liquid glyceride oil is soybean oil with an Iodine Value of from about to about 120, the monoester of propylene glycol is monostearate, the normally solid triglyceride fat is substantially completely hydrogenated soybean oil and the fatty acid is stearic acid.
3. A stable fluid shortening composition, suitable for use in the preparation of recipe cake batters with a single mixing step in large scale commercial baking operations, which comprises soybean oil hydrogenated to an Iodine Value of from about 100 to about having therein from about 3% to 5%, by weight of the composition of propylene glycol monostearate, said shortening composition additionally comprising, by weight of the composition, from about 1% to about 3% substantially completely hydrogenated soybean oil, from about 3% to about 4% normally solid partial ester of glycerine and substantially saturated fatty acid having from 14 to 22 carbon atoms, and from about 0.6% to about 2% of stearic acid, said substantially completely hydrogenated soybean oil and said partial ester of glycerine being at least 80% in beta phase, said shortening being substantially free from intermediate melting solids.
References Cited in the file of this patent UNITED STATES PATENTS 2,061,121 Votaw et al Nov. 17, 1936 2,508,393 Jaeger May 23, 1950 2,815,286 Andre et al Dec. 3, 1957 I 2,868,652 Brock Jan. 13, 1959 2,909,432 Linteris Oct. 20, 1959 3,011,896 Eber et al. Dec. 5, 1961 3,097,098 Allen et a1 July 9, 1963
Claims (1)
1. A STABLE FLUID SHORTENING COMPOSITION, SUITABLE FOR USE IN THE PREPARATION OF RECIPE CAKE BATTERS WITH A SINGLE MIXING STEP IN LARGE SCALE COMMERCIAL BAKING OPERATIONS, WHICH COMPRISES A NORMALLY LIQUID GLYCERIDE OIL HAVING THEREIN FROM ABOUT 0.5% TO ABOUT 8% BY WEIGHT OF THE COMPOSITION, OF MONO-ESTER OF PROPYLENE GLYCOL AND SATURATED FATTY ACID CONTAINING FROM 14 TO 22 CARBON ATOMS, SAID SHORTENING COMPOSITION ADDITIONALLY COMPRISING, BY WEIGHT OF THE COMPOSITION, FROM ABOUT 1% TO ABOUT 5% NORMALLY SOLID TRIGLYCERIDE FAT AND FROM ABOUT .5% TO ABOUT 10% OF SATURATED FATTY ACID HAVING FROM 14 TO 22 CARBON ATOMS, SAID TRIGLYCERIDE FAT BEING AT LEAST 80% IN BETA PHASE.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US182843A US3145110A (en) | 1962-03-27 | 1962-03-27 | Shortening product |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US182843A US3145110A (en) | 1962-03-27 | 1962-03-27 | Shortening product |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US3145110A true US3145110A (en) | 1964-08-18 |
Family
ID=22670279
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US182843A Expired - Lifetime US3145110A (en) | 1962-03-27 | 1962-03-27 | Shortening product |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US3145110A (en) |
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3402050A (en) * | 1965-06-11 | 1968-09-17 | Procter & Gamble | All purpose-shortening |
| US3458323A (en) * | 1965-06-28 | 1969-07-29 | Procter & Gamble | Culinary composition containing alkyl phosphoryl halides |
| US3528823A (en) * | 1966-08-04 | 1970-09-15 | Lever Brothers Ltd | Fluid shortening |
| US3549383A (en) * | 1967-11-16 | 1970-12-22 | Procter & Gamble | Fluid shortening for cakes and cream icings |
| US4391838A (en) * | 1981-11-13 | 1983-07-05 | Scm Corporation | Process for continuous fluidization of shortening |
| US4419377A (en) * | 1982-03-22 | 1983-12-06 | The Procter & Gamble Company | Cake mix containing a lipophilic emulsifier system |
| US5211981A (en) * | 1991-06-13 | 1993-05-18 | The Procter & Gamble Company | Process for making a uniform liquid, pourable shortening containing high emulsifier levels |
Citations (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2061121A (en) * | 1932-10-03 | 1936-11-17 | Procter & Gamble | Baked goods and process of making same |
| US2508393A (en) * | 1943-11-19 | 1950-05-23 | Edward B Jaeger | Shortening |
| US2815286A (en) * | 1955-10-28 | 1957-12-03 | Procter & Gamble | Liquid shortening |
| US2868652A (en) * | 1954-09-17 | 1959-01-13 | Staley Mfg Co A E | Liquid shortening and method of making same |
| US2909432A (en) * | 1957-02-11 | 1959-10-20 | Lever Brothers Ltd | Fluid shortening |
| US3011896A (en) * | 1960-01-19 | 1961-12-05 | Glidden Co | Fluid shortening and process for making the same |
| US3097098A (en) * | 1960-06-30 | 1963-07-09 | Anderson Clayton & Co | Shortening and agent therefor |
-
1962
- 1962-03-27 US US182843A patent/US3145110A/en not_active Expired - Lifetime
Patent Citations (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2061121A (en) * | 1932-10-03 | 1936-11-17 | Procter & Gamble | Baked goods and process of making same |
| US2508393A (en) * | 1943-11-19 | 1950-05-23 | Edward B Jaeger | Shortening |
| US2868652A (en) * | 1954-09-17 | 1959-01-13 | Staley Mfg Co A E | Liquid shortening and method of making same |
| US2815286A (en) * | 1955-10-28 | 1957-12-03 | Procter & Gamble | Liquid shortening |
| US2909432A (en) * | 1957-02-11 | 1959-10-20 | Lever Brothers Ltd | Fluid shortening |
| US3011896A (en) * | 1960-01-19 | 1961-12-05 | Glidden Co | Fluid shortening and process for making the same |
| US3097098A (en) * | 1960-06-30 | 1963-07-09 | Anderson Clayton & Co | Shortening and agent therefor |
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3402050A (en) * | 1965-06-11 | 1968-09-17 | Procter & Gamble | All purpose-shortening |
| US3458323A (en) * | 1965-06-28 | 1969-07-29 | Procter & Gamble | Culinary composition containing alkyl phosphoryl halides |
| US3528823A (en) * | 1966-08-04 | 1970-09-15 | Lever Brothers Ltd | Fluid shortening |
| US3549383A (en) * | 1967-11-16 | 1970-12-22 | Procter & Gamble | Fluid shortening for cakes and cream icings |
| US4391838A (en) * | 1981-11-13 | 1983-07-05 | Scm Corporation | Process for continuous fluidization of shortening |
| US4419377A (en) * | 1982-03-22 | 1983-12-06 | The Procter & Gamble Company | Cake mix containing a lipophilic emulsifier system |
| US5211981A (en) * | 1991-06-13 | 1993-05-18 | The Procter & Gamble Company | Process for making a uniform liquid, pourable shortening containing high emulsifier levels |
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