DE3529564A1 - Process for producing a fat-free deep-fried material - Google Patents
Process for producing a fat-free deep-fried materialInfo
- Publication number
- DE3529564A1 DE3529564A1 DE19853529564 DE3529564A DE3529564A1 DE 3529564 A1 DE3529564 A1 DE 3529564A1 DE 19853529564 DE19853529564 DE 19853529564 DE 3529564 A DE3529564 A DE 3529564A DE 3529564 A1 DE3529564 A1 DE 3529564A1
- Authority
- DE
- Germany
- Prior art keywords
- deep
- jojoba oil
- frying
- fat
- fried material
- 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.)
- Withdrawn
Links
Classifications
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
- A23L5/00—Preparation or treatment of foods or foodstuffs, in general; Food or foodstuffs obtained thereby; Materials therefor
- A23L5/10—General methods of cooking foods, e.g. by roasting or frying
- A23L5/11—General methods of cooking foods, e.g. by roasting or frying using oil
Abstract
Description
Die Erfindung betrifft ein Verfahren zur Herstellung eines nach den üblichen Methoden produzierten beliebigen Frittier gutes, das jedoch nicht durch die normalerweise unvermeid liche Fettaufnahme beim Frittieren den Kalorieengehalt des Frittiergutes erhöht. Dadurch ist dieses bekömmlicher und gesünder.The invention relates to a method for producing a Any fryer produced according to the usual methods good, but not usually inevitable fat intake when frying the calorie content of the Food to be fried increased. This makes it more digestible and healthier.
Diese Vorteile sind zu erreichen, indem für das Fritten statt der üblicherweise verwendeten pflanzlichen oder tie rischen Triglyceride ein bei Normaltemperatur flüssiges Wachs verwendet wird. Dieses Wachs, üblicherweise - nicht ganz korrekt - Jojobaöl (simmondsia chinensis - Buxaceae -) genannt, stammt aus der Jojobanuß, eine ca. olivengroße Frucht, die an einem Wüstenstrauch wächst. Durch einfaches Auspressen (50% Öl, 50% Ölkuchen) wird das Öl, welches den ungewöhnlich hohen, so vorteilhaften Kp von 662 Grad Kalvin besitzt, gewonnen.These advantages can be achieved by using a wax that is liquid at normal temperature for the frit instead of the vegetable or tie triglycerides commonly used. This wax, usually - not quite correctly - called jojoba oil (simmondsia chinensis - Buxaceae -) comes from jojoba nut, an olive-sized fruit that grows on a desert shrub. By simply squeezing (50% oil, 50% oil cake) the oil, which has the unusually high, so advantageous Kp of 662 degrees Kalvin, is obtained.
Es ist bekannt, daß durch mehr oder minder langdauerndes Eintauchen in heißes Fett die verschiedenen Frittiergü ter in fast beliebig kleinen (Haushalt) oder industriell auch in größeren Chargen hergestellt werden können. Die se üblicherweise angewendeten Verfahren haben zwei gravie rende Nachteile.It is known that by more or less long-lasting Immerse the various deep-fry products in hot fat ter in almost any small (household) or industrial can also be produced in larger batches. The The methods usually used have two gravies disadvantages.
- A Durch die unvermeidliche Aufnahme des Frittierfettes in das Frittiergut wird dieses in seinem Kalorieen gehalt - besonders bei Kartoffel- und Teigprodukten aller Art - oft signifikant (jedoch meist sehr uner wünschtermaßen) erhöht.A Due to the inevitable absorption of frying fat in the fried food this is in its calories content - especially for potato and dough products of all kinds - often significant (but mostly very little desirably) increased.
- B Durch längeres oder mehrmaliges Benutzen des Frit tierfettes wird dieses (durch Abbau-, Zersetzungs-, Krack- und Reaktionsproduktenbildung mit dem Frittiergut) bald unbrauchbar beziehungsweise bekommt das Frit tiergut einen spezifischen, unangenehmen Geschmack, abgesehen von den physiologischen nachteiligen Fol gen zu lange im Einsatz gewesenen Frittierungsfet tes, das ja beim Verzehr mit dem Frittiergut geges sen wird.B By using the frit for a long time or several times animal fat is this (through degradation, decomposition, Cracking and reaction product formation with the fried food) soon useless or gets the frit animal goods have a specific, unpleasant taste, apart from the physiological adverse fol frying fat that has been in use for too long tes that is eaten with the fried food when eaten will.
Diese gravierenden Nachteile werden durch den Einsatz des oben vorgeschlagenen Jojobaöls als Frittierungsmit tel (bei sonst gleichen Verfahrensbedingungen) voll kommen vermieden.These serious disadvantages are caused by the use of the jojoba oil proposed above as a deep-frying agent tel (otherwise the same process conditions) full come avoided.
Das Jojobaöl ist physiologisch gut verträglich (als Arze neimittel und in der Kosmetik bereits eingesetzt) und wird, da es als Wachs keine Triglyceride enthält, im menschlichen Körper nicht abgebaut. Außerdem lassen sich die unter B aufgeführten Nachteile besonders für die Gesundheit auf Grund des deutlich mehr als 100 Grad höheren K p des Jojobaöls gegenüber den Speisefetten und seiner extrem guten thermischen Stabilität vollkommen vermeiden.Jojoba oil is physiologically well tolerated (as a drug and already used in cosmetics) and, as it contains no triglycerides as wax, is not broken down in the human body. In addition, the disadvantages listed under B, especially for health, can be completely avoided due to the significantly higher K p of jojoba oil compared to edible fats and its extremely good thermal stability.
Claims (3)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE19853529564 DE3529564A1 (en) | 1985-08-17 | 1985-08-17 | Process for producing a fat-free deep-fried material |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE19853529564 DE3529564A1 (en) | 1985-08-17 | 1985-08-17 | Process for producing a fat-free deep-fried material |
Publications (1)
Publication Number | Publication Date |
---|---|
DE3529564A1 true DE3529564A1 (en) | 1987-03-12 |
Family
ID=6278791
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DE19853529564 Withdrawn DE3529564A1 (en) | 1985-08-17 | 1985-08-17 | Process for producing a fat-free deep-fried material |
Country Status (1)
Country | Link |
---|---|
DE (1) | DE3529564A1 (en) |
Cited By (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4927658A (en) * | 1989-02-16 | 1990-05-22 | Nabisco Brands, Inc. | Tris-hydroxymethyl alkane esters as low calorie fat mimetics |
US4927659A (en) * | 1989-02-16 | 1990-05-22 | Nabisco Brands, Inc. | Tris-hydroxymethyl lower alkane esters as fat mimetics |
US4992292A (en) * | 1989-02-16 | 1991-02-12 | Nabisco Brands, Inc. | Tris-hydroxymethyl alkane dicarboxylate extended esters as low calorie fat mimetics |
US5043179A (en) * | 1990-03-29 | 1991-08-27 | Nabisco Brands, Inc. | Triol triester derivatives as low calorie fat mimetics |
US5063075A (en) * | 1990-08-01 | 1991-11-05 | Nabisco Brands, Inc. | Amide ether derivatives as low calorie fat mimetics |
US5068120A (en) * | 1990-08-01 | 1991-11-26 | Nabisco Brands, Inc. | Amine ester derivatives as low calorie fat mimetics |
US5068119A (en) * | 1990-09-28 | 1991-11-26 | Nabisco Brands, Inc. | Acid-hydrolyzable ester derivatives as low calorie fat mimetics |
US5082683A (en) * | 1990-08-01 | 1992-01-21 | Nabisco Brands, Inc. | Amide/amine ester derivatives as low calorie fat mimetics |
US5124166A (en) * | 1987-08-13 | 1992-06-23 | Nabisco, Inc. | Carboxy/carboxylate disubstituted esters as edible fat mimetics |
US5169665A (en) * | 1990-04-17 | 1992-12-08 | Nabisco, Inc. | Tris-hydroxymethyl alkane esters as low calorie fat mimetics |
US5219604A (en) * | 1991-02-13 | 1993-06-15 | Nabisco, Inc. | Use of ester-bridged side chains to suppress caloric availability of fat compounds |
US5286512A (en) * | 1989-06-27 | 1994-02-15 | Nabisco, Inc. | Diol lipid analogues as edible fat replacements |
EP1429794A1 (en) * | 2001-09-07 | 2004-06-23 | International Flora Technologies, Ltd. | Weight reduction and maintenance method for animals |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0067358B1 (en) * | 1981-06-12 | 1984-02-29 | Societe Des Produits Nestle S.A. | Low calorie food composition |
-
1985
- 1985-08-17 DE DE19853529564 patent/DE3529564A1/en not_active Withdrawn
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0067358B1 (en) * | 1981-06-12 | 1984-02-29 | Societe Des Produits Nestle S.A. | Low calorie food composition |
Non-Patent Citations (1)
Title |
---|
HAMM, D.J.: Preparation of ... Jojoba Oil ... as Low Calorie Replacements of Edible Fats and Oils, in J. Food Science, Bd.49, 1984, S.419-28 * |
Cited By (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5124166A (en) * | 1987-08-13 | 1992-06-23 | Nabisco, Inc. | Carboxy/carboxylate disubstituted esters as edible fat mimetics |
US4927659A (en) * | 1989-02-16 | 1990-05-22 | Nabisco Brands, Inc. | Tris-hydroxymethyl lower alkane esters as fat mimetics |
US4992292A (en) * | 1989-02-16 | 1991-02-12 | Nabisco Brands, Inc. | Tris-hydroxymethyl alkane dicarboxylate extended esters as low calorie fat mimetics |
US4927658A (en) * | 1989-02-16 | 1990-05-22 | Nabisco Brands, Inc. | Tris-hydroxymethyl alkane esters as low calorie fat mimetics |
US5286512A (en) * | 1989-06-27 | 1994-02-15 | Nabisco, Inc. | Diol lipid analogues as edible fat replacements |
US5043179A (en) * | 1990-03-29 | 1991-08-27 | Nabisco Brands, Inc. | Triol triester derivatives as low calorie fat mimetics |
US5169665A (en) * | 1990-04-17 | 1992-12-08 | Nabisco, Inc. | Tris-hydroxymethyl alkane esters as low calorie fat mimetics |
US5082683A (en) * | 1990-08-01 | 1992-01-21 | Nabisco Brands, Inc. | Amide/amine ester derivatives as low calorie fat mimetics |
US5068120A (en) * | 1990-08-01 | 1991-11-26 | Nabisco Brands, Inc. | Amine ester derivatives as low calorie fat mimetics |
US5063075A (en) * | 1990-08-01 | 1991-11-05 | Nabisco Brands, Inc. | Amide ether derivatives as low calorie fat mimetics |
US5068119A (en) * | 1990-09-28 | 1991-11-26 | Nabisco Brands, Inc. | Acid-hydrolyzable ester derivatives as low calorie fat mimetics |
US5219604A (en) * | 1991-02-13 | 1993-06-15 | Nabisco, Inc. | Use of ester-bridged side chains to suppress caloric availability of fat compounds |
EP1429794A1 (en) * | 2001-09-07 | 2004-06-23 | International Flora Technologies, Ltd. | Weight reduction and maintenance method for animals |
EP1429794A4 (en) * | 2001-09-08 | 2004-11-10 | Int Flora Technologies Ltd | Weight reduction and maintenance method for animals |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
8110 | Request for examination paragraph 44 | ||
8130 | Withdrawal |