JP7623945B2 - Release oil for processed meat foods - Google Patents
Release oil for processed meat foods Download PDFInfo
- Publication number
- JP7623945B2 JP7623945B2 JP2021550556A JP2021550556A JP7623945B2 JP 7623945 B2 JP7623945 B2 JP 7623945B2 JP 2021550556 A JP2021550556 A JP 2021550556A JP 2021550556 A JP2021550556 A JP 2021550556A JP 7623945 B2 JP7623945 B2 JP 7623945B2
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- JP
- Japan
- Prior art keywords
- mass
- oil
- enzymatically decomposed
- release oil
- lecithin
- 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.)
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- 235000013305 food Nutrition 0.000 title claims description 46
- 235000020991 processed meat Nutrition 0.000 title claims description 30
- 239000003921 oil Substances 0.000 claims description 53
- IIZPXYDJLKNOIY-JXPKJXOSSA-N 1-palmitoyl-2-arachidonoyl-sn-glycero-3-phosphocholine Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@H](COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCC\C=C/C\C=C/C\C=C/C\C=C/CCCCC IIZPXYDJLKNOIY-JXPKJXOSSA-N 0.000 claims description 46
- 239000000787 lecithin Substances 0.000 claims description 46
- 229940067606 lecithin Drugs 0.000 claims description 46
- 235000010445 lecithin Nutrition 0.000 claims description 46
- 235000013372 meat Nutrition 0.000 claims description 25
- 235000014593 oils and fats Nutrition 0.000 claims description 21
- 150000003904 phospholipids Chemical class 0.000 claims description 19
- 235000015220 hamburgers Nutrition 0.000 claims description 18
- 238000000034 method Methods 0.000 claims description 14
- PORPENFLTBBHSG-MGBGTMOVSA-N 1,2-dihexadecanoyl-sn-glycerol-3-phosphate Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@H](COP(O)(O)=O)OC(=O)CCCCCCCCCCCCCCC PORPENFLTBBHSG-MGBGTMOVSA-N 0.000 claims description 12
- 238000010411 cooking Methods 0.000 claims description 12
- 239000008157 edible vegetable oil Substances 0.000 claims description 11
- 239000003925 fat Substances 0.000 claims description 10
- 238000004519 manufacturing process Methods 0.000 claims description 7
- 239000003795 chemical substances by application Substances 0.000 claims description 6
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- -1 medium-chain fatty acid triglycerides Chemical class 0.000 description 19
- 235000014113 dietary fatty acids Nutrition 0.000 description 16
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- 239000000194 fatty acid Substances 0.000 description 16
- 238000011156 evaluation Methods 0.000 description 11
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- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 6
- JZNWSCPGTDBMEW-UHFFFAOYSA-N Glycerophosphorylethanolamin Natural products NCCOP(O)(=O)OCC(O)CO JZNWSCPGTDBMEW-UHFFFAOYSA-N 0.000 description 6
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 6
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 6
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- 239000005642 Oleic acid Substances 0.000 description 3
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- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 3
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- 241000251468 Actinopterygii Species 0.000 description 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
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- UKMSUNONTOPOIO-UHFFFAOYSA-N docosanoic acid Chemical compound CCCCCCCCCCCCCCCCCCCCCC(O)=O UKMSUNONTOPOIO-UHFFFAOYSA-N 0.000 description 2
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- DNIAPMSPPWPWGF-UHFFFAOYSA-N monopropylene glycol Natural products CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 2
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- WBHHMMIMDMUBKC-XLNAKTSKSA-N ricinelaidic acid Chemical class CCCCCC[C@@H](O)C\C=C\CCCCCCCC(O)=O WBHHMMIMDMUBKC-XLNAKTSKSA-N 0.000 description 2
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- 229930003231 vitamin Natural products 0.000 description 2
- 229940088594 vitamin Drugs 0.000 description 2
- JQWAHKMIYCERGA-UHFFFAOYSA-N (2-nonanoyloxy-3-octadeca-9,12-dienoyloxypropoxy)-[2-(trimethylazaniumyl)ethyl]phosphinate Chemical compound CCCCCCCCC(=O)OC(COP([O-])(=O)CC[N+](C)(C)C)COC(=O)CCCCCCCC=CCC=CCCCCC JQWAHKMIYCERGA-UHFFFAOYSA-N 0.000 description 1
- ASWBNKHCZGQVJV-UHFFFAOYSA-N (3-hexadecanoyloxy-2-hydroxypropyl) 2-(trimethylazaniumyl)ethyl phosphate Chemical compound CCCCCCCCCCCCCCCC(=O)OCC(O)COP([O-])(=O)OCC[N+](C)(C)C ASWBNKHCZGQVJV-UHFFFAOYSA-N 0.000 description 1
- BJEPYKJPYRNKOW-REOHCLBHSA-N (S)-malic acid Chemical compound OC(=O)[C@@H](O)CC(O)=O BJEPYKJPYRNKOW-REOHCLBHSA-N 0.000 description 1
- LDVVTQMJQSCDMK-UHFFFAOYSA-N 1,3-dihydroxypropan-2-yl formate Chemical compound OCC(CO)OC=O LDVVTQMJQSCDMK-UHFFFAOYSA-N 0.000 description 1
- JLPULHDHAOZNQI-ZTIMHPMXSA-N 1-hexadecanoyl-2-(9Z,12Z-octadecadienoyl)-sn-glycero-3-phosphocholine Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@H](COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCCCCCC\C=C/C\C=C/CCCCC JLPULHDHAOZNQI-ZTIMHPMXSA-N 0.000 description 1
- FPIPGXGPPPQFEQ-UHFFFAOYSA-N 13-cis retinol Natural products OCC=C(C)C=CC=C(C)C=CC1=C(C)CCCC1(C)C FPIPGXGPPPQFEQ-UHFFFAOYSA-N 0.000 description 1
- ZIIUUSVHCHPIQD-UHFFFAOYSA-N 2,4,6-trimethyl-N-[3-(trifluoromethyl)phenyl]benzenesulfonamide Chemical compound CC1=CC(C)=CC(C)=C1S(=O)(=O)NC1=CC=CC(C(F)(F)F)=C1 ZIIUUSVHCHPIQD-UHFFFAOYSA-N 0.000 description 1
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- 235000011301 Brassica oleracea var capitata Nutrition 0.000 description 1
- 235000001169 Brassica oleracea var oleracea Nutrition 0.000 description 1
- DPUOLQHDNGRHBS-UHFFFAOYSA-N Brassidinsaeure Natural products CCCCCCCCC=CCCCCCCCCCCCC(O)=O DPUOLQHDNGRHBS-UHFFFAOYSA-N 0.000 description 1
- 240000004160 Capsicum annuum Species 0.000 description 1
- 235000008534 Capsicum annuum var annuum Nutrition 0.000 description 1
- 241000282693 Cercopithecidae Species 0.000 description 1
- 244000000626 Daucus carota Species 0.000 description 1
- 235000002767 Daucus carota Nutrition 0.000 description 1
- 239000004278 EU approved seasoning Substances 0.000 description 1
- 102000004190 Enzymes Human genes 0.000 description 1
- 108090000790 Enzymes Proteins 0.000 description 1
- URXZXNYJPAJJOQ-UHFFFAOYSA-N Erucic acid Natural products CCCCCCC=CCCCCCCCCCCCC(O)=O URXZXNYJPAJJOQ-UHFFFAOYSA-N 0.000 description 1
- QAQJMLQRFWZOBN-LAUBAEHRSA-N L-ascorbyl-6-palmitate Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@H](O)[C@H]1OC(=O)C(O)=C1O QAQJMLQRFWZOBN-LAUBAEHRSA-N 0.000 description 1
- 239000011786 L-ascorbyl-6-palmitate Substances 0.000 description 1
- 235000019687 Lamb Nutrition 0.000 description 1
- 235000019483 Peanut oil Nutrition 0.000 description 1
- 241001494479 Pecora Species 0.000 description 1
- 102000015439 Phospholipases Human genes 0.000 description 1
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- 244000061458 Solanum melongena Species 0.000 description 1
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- 244000299461 Theobroma cacao Species 0.000 description 1
- 235000005764 Theobroma cacao ssp. cacao Nutrition 0.000 description 1
- 235000005767 Theobroma cacao ssp. sphaerocarpum Nutrition 0.000 description 1
- FPIPGXGPPPQFEQ-BOOMUCAASA-N Vitamin A Natural products OC/C=C(/C)\C=C\C=C(\C)/C=C/C1=C(C)CCCC1(C)C FPIPGXGPPPQFEQ-BOOMUCAASA-N 0.000 description 1
- 229930003316 Vitamin D Natural products 0.000 description 1
- QYSXJUFSXHHAJI-XFEUOLMDSA-N Vitamin D3 Natural products C1(/[C@@H]2CC[C@@H]([C@]2(CCC1)C)[C@H](C)CCCC(C)C)=C/C=C1\C[C@@H](O)CCC1=C QYSXJUFSXHHAJI-XFEUOLMDSA-N 0.000 description 1
- 235000018936 Vitellaria paradoxa Nutrition 0.000 description 1
- 241001135917 Vitellaria paradoxa Species 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- FPIPGXGPPPQFEQ-OVSJKPMPSA-N all-trans-retinol Chemical compound OC\C=C(/C)\C=C\C=C(/C)\C=C\C1=C(C)CCCC1(C)C FPIPGXGPPPQFEQ-OVSJKPMPSA-N 0.000 description 1
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- 238000004458 analytical method Methods 0.000 description 1
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- 235000001046 cacaotero Nutrition 0.000 description 1
- OEUVSBXAMBLPES-UHFFFAOYSA-L calcium stearoyl-2-lactylate Chemical compound [Ca+2].CCCCCCCCCCCCCCCCCC(=O)OC(C)C(=O)OC(C)C([O-])=O.CCCCCCCCCCCCCCCCCC(=O)OC(C)C(=O)OC(C)C([O-])=O OEUVSBXAMBLPES-UHFFFAOYSA-L 0.000 description 1
- 210000004027 cell Anatomy 0.000 description 1
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- 235000019864 coconut oil Nutrition 0.000 description 1
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- 150000002009 diols Chemical class 0.000 description 1
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- DPUOLQHDNGRHBS-KTKRTIGZSA-N erucic acid Chemical compound CCCCCCCC\C=C/CCCCCCCCCCCC(O)=O DPUOLQHDNGRHBS-KTKRTIGZSA-N 0.000 description 1
- 150000002148 esters Chemical group 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 235000021323 fish oil Nutrition 0.000 description 1
- 239000000796 flavoring agent Substances 0.000 description 1
- 235000019634 flavors Nutrition 0.000 description 1
- 235000012041 food component Nutrition 0.000 description 1
- 239000005417 food ingredient Substances 0.000 description 1
- 235000011194 food seasoning agent Nutrition 0.000 description 1
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- 239000003349 gelling agent Substances 0.000 description 1
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- 229910052742 iron Inorganic materials 0.000 description 1
- 229940069445 licorice extract Drugs 0.000 description 1
- 239000000944 linseed oil Substances 0.000 description 1
- 235000021388 linseed oil Nutrition 0.000 description 1
- 239000001630 malic acid Substances 0.000 description 1
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- 229910052751 metal Inorganic materials 0.000 description 1
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- 150000007524 organic acids Chemical class 0.000 description 1
- 239000003346 palm kernel oil Substances 0.000 description 1
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- 239000002245 particle Substances 0.000 description 1
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- 239000000312 peanut oil Substances 0.000 description 1
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- 238000012545 processing Methods 0.000 description 1
- 238000011002 quantification Methods 0.000 description 1
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- 229960003656 ricinoleic acid Drugs 0.000 description 1
- FEUQNCSVHBHROZ-UHFFFAOYSA-N ricinoleic acid Natural products CCCCCCC(O[Si](C)(C)C)CC=CCCCCCCCC(=O)OC FEUQNCSVHBHROZ-UHFFFAOYSA-N 0.000 description 1
- 229940092258 rosemary extract Drugs 0.000 description 1
- 235000020748 rosemary extract Nutrition 0.000 description 1
- 239000001233 rosmarinus officinalis l. extract Substances 0.000 description 1
- 235000015067 sauces Nutrition 0.000 description 1
- 229940057910 shea butter Drugs 0.000 description 1
- 239000000779 smoke Substances 0.000 description 1
- 229940083466 soybean lecithin Drugs 0.000 description 1
- 235000013599 spices Nutrition 0.000 description 1
- 239000003760 tallow Substances 0.000 description 1
- 235000013616 tea Nutrition 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 235000010384 tocopherol Nutrition 0.000 description 1
- 229960001295 tocopherol Drugs 0.000 description 1
- 229930003799 tocopherol Natural products 0.000 description 1
- 239000011732 tocopherol Substances 0.000 description 1
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- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- GVJHHUAWPYXKBD-IEOSBIPESA-N α-tocopherol Chemical compound OC1=C(C)C(C)=C2O[C@@](CCC[C@H](C)CCC[C@H](C)CCCC(C)C)(C)CCC2=C1C GVJHHUAWPYXKBD-IEOSBIPESA-N 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 OR COOKING OILS
- A23D9/00—Other edible oils or fats, e.g. shortenings or cooking oils
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES, NOT OTHERWISE PROVIDED FOR; PREPARATION OR TREATMENT THEREOF
- A23L13/00—Meat products; Meat meal; Preparation or treatment thereof
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES, NOT OTHERWISE PROVIDED FOR; PREPARATION OR TREATMENT THEREOF
- A23L13/00—Meat products; Meat meal; Preparation or treatment thereof
- A23L13/10—Meat meal or powder; Granules, agglomerates or flakes
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES, NOT OTHERWISE PROVIDED FOR; PREPARATION OR TREATMENT THEREOF
- A23L35/00—Foods or foodstuffs not provided for in groups A23L5/00 - A23L33/00; Preparation or treatment thereof
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Food Science & Technology (AREA)
- Polymers & Plastics (AREA)
- Health & Medical Sciences (AREA)
- Nutrition Science (AREA)
- Zoology (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Meat, Egg Or Seafood Products (AREA)
- Seeds, Soups, And Other Foods (AREA)
Description
本発明は、食肉加工食品用の離型油、食肉加工食品の焦げ付き抑制方法、食肉加工食品の焦げ付き抑制剤、及び食肉加工食品の製造方法に関する。 The present invention relates to a release oil for processed meat foods, a method for preventing processed meat foods from burning, an agent for preventing processed meat foods from burning, and a method for producing processed meat foods.
従来、食品加工業界において、加熱調理の際、焼成後の食品素材と調理器具、焼型、天板などとの付着を防止する目的で、離型油が使用されている。 Traditionally, in the food processing industry, release oils have been used during cooking to prevent food ingredients from sticking to cooking utensils, baking molds, baking trays, etc. after cooking.
離型油には、食品の離型性を得るために、経済性と効果の点から、レシチンが一般的に使用されてきた。しかし、レシチンを使用した離型油は、加熱による褐変が起こりやすく、調理品の風味や外観を損なうという課題があった。また、調理品によっては離型性が十分ではなかった。Lecithin has been commonly used as a release oil to achieve food release properties, due to its economical and effective properties. However, release oils that use lecithin have the problem that they tend to brown when heated, impairing the flavor and appearance of cooked foods. In addition, the release properties are insufficient for some cooked foods.
特許文献1には、レシチンを0.05重量%以上5重量%以下含有する炒め用油脂組成物が記載されている。しかし、上記特許文献1には食肉加工食品の離型性については開示も示唆もない。 Patent Document 1 describes a stir-frying oil composition containing 0.05% by weight or more and 5% by weight or less of lecithin. However, Patent Document 1 does not disclose or suggest anything about the releasability of processed meat foods.
そこで、本発明においては、食肉加工食品用離型油、食肉加工食品の焦げ付き抑制方法、食肉加工食品の焦げ付き抑制剤、及び食肉加工食品の製造方法を提供することを目的とする。Therefore, the present invention aims to provide a release oil for processed meat foods, a method for preventing processed meat foods from burning, an agent for preventing processed meat foods from burning, and a method for producing processed meat foods.
本発明者等は、鋭意検討の結果、食用油脂に、特定のレシチンを含有させた離型油が、食肉加工食品の加熱調理時の焦げ付きを抑制することを見出し、本発明を完成させた。 After extensive research, the inventors discovered that a release oil made from edible oils and fats containing a specific type of lecithin prevents processed meat foods from burning when cooked, and thus completed the present invention.
すなわち、本発明は、その第1の観点において、食用油脂と、酵素分解レシチンを含有する食肉加工食品用離型油であって、前記酵素分解レシチンをリン脂質として、0.01質量%以上4.5質量%以下含有する、前記離型油を提供するものである。That is, in a first aspect, the present invention provides a release oil for processed meat foods, which contains edible oils and fats and enzymatically decomposed lecithin, and which contains the enzymatically decomposed lecithin in an amount of 0.01% by mass or more and 4.5% by mass or less as phospholipids.
本発明にかかる離型油においては、前記酵素分解レシチン中のリン脂質に対するホスファチジン酸含量が50質量%以上100質量%以下であることが好ましい。In the release oil of the present invention, it is preferable that the phosphatidic acid content relative to the phospholipids in the enzymatically decomposed lecithin is 50% by mass or more and 100% by mass or less.
本発明にかかる離型油においては、前記食肉加工食品が、ひき肉を含む食品であることが好ましい。In the release oil of the present invention, it is preferable that the processed meat food is a food containing minced meat.
本発明にかかる離型油においては、前記ひき肉を含む食品が、ハンバーグ、肉団子、つくね、ミートローフ、及びひき肉炒めから選ばれる1種であることが好ましい。In the release oil of the present invention, it is preferable that the food containing minced meat is one selected from hamburger steak, meatballs, meatballs, meatloaf, and stir-fried minced meat.
また、本発明は、その第2の観点において、前記離型油を、食肉加工食品の加熱調理に使用する、焦げ付き抑制方法を提供するものである。In addition, in its second aspect, the present invention provides a method for preventing burning by using the release oil in the cooking of processed meat foods.
また、本発明は、その第3の観点において、前記離型油を有効成分とする、食肉加工食品の焦げ付き抑制剤を提供するものである。 In addition, in its third aspect, the present invention provides an anti-sticking agent for processed meat foods, which contains the release oil as an active ingredient.
また、本発明は、その第4の観点において、前記離型油を加熱調理に使用する工程を含む、食肉加工食品の製造方法を提供するものである。 In a fourth aspect, the present invention provides a method for producing processed meat foods, which includes a step of using the release oil for cooking.
本発明によれば、食肉加工食品の加熱調理時の焦げ付きを抑制できる離型油を提供することができる。また、その離型油を利用して、食肉加工食品の加熱調理時の焦げ付き抑制方法、ならびに食肉加工食品の焦げ付き抑制剤を提供することができる。さらに、離型油を加熱調理に使用する工程を含む食肉加工食品の製造方法を提供することができる。 According to the present invention, it is possible to provide a release oil that can suppress burning of processed meat foods during cooking. In addition, it is possible to provide a method for suppressing burning of processed meat foods during cooking by using the release oil, as well as an agent for suppressing burning of processed meat foods. Furthermore, it is possible to provide a method for producing processed meat foods that includes a step of using the release oil for cooking.
本発明にかかる離型油は食用油脂を含む。前記食用油脂に用いられる原料油脂としては、特に限定されないが、例えば、菜種油、大豆油、コーン油、ヤシ油、パーム油、パーム核油、サル脂、カカオ脂、シア脂、米油、綿実油、紅花油、ヒマワリ油、オリーブ油、亜麻仁油、落花生油などの植物油脂、牛脂、豚脂、鶏脂、乳脂、魚油などの動物油脂、中鎖脂肪酸トリグリセリドなどの合成油脂が挙げられる。また、前記植物油脂、動物油脂又は合成油脂に対して、硬化、分別、及びエステル交換から選ばれる1種又は2種以上の処理をした加工油脂を原料油脂として使用することができる。前記食用油脂は、これらの油脂から1種又は2種以上を選択して用いることができるが、食用油脂は、大豆油、菜種油、パーム系油脂、コーン油、ヒマワリ油、オリーブ油、綿実油、米油、及び紅花油から選ばれる1種又は2種以上を含むことが好ましく、大豆油、菜種油、及びパーム系油脂から選ばれる1種又は2種以上を含むことがより好ましい。その場合、食用油脂中の大豆油、菜種油、パーム系油脂、コーン油、ヒマワリ油、オリーブ油、綿実油、米油、及び紅花油から選ばれる1種又は2種以上の含有量の合計が、60質量%以上100質量%以下であることが好ましく、75質量%以上100質量%以下であることがより好ましく、90質量%以上100質量%以下であることがさらに好ましく、100質量%であることがさらにより好ましい。ここでいうパーム系油脂とは、パーム油及びパーム油の加工油脂を意味する。The release oil according to the present invention includes edible oils and fats. The raw oils and fats used for the edible oils and fats are not particularly limited, but examples thereof include vegetable oils and fats such as rapeseed oil, soybean oil, corn oil, coconut oil, palm oil, palm kernel oil, monkey fat, cacao butter, shea butter, rice oil, cottonseed oil, safflower oil, sunflower oil, olive oil, linseed oil, and peanut oil, animal oils and fats such as beef tallow, lard, chicken fat, milk fat, and fish oil, and synthetic oils and fats such as medium-chain fatty acid triglycerides. In addition, processed oils and fats obtained by subjecting the vegetable oils and fats, animal oils and fats, or synthetic oils and fats to one or more treatments selected from hardening, fractionation, and ester exchange can be used as the raw oils and fats. The edible oils and fats may be one or more selected from these oils and fats, and the edible oils and fats preferably contain one or more selected from soybean oil, rapeseed oil, palm-based oils and fats, corn oil, sunflower oil, olive oil, cottonseed oil, rice oil, and safflower oil, and more preferably contain one or more selected from soybean oil, rapeseed oil, and palm-based oils and fats. In this case, the total content of one or more selected from soybean oil, rapeseed oil, palm-based oils and fats, corn oil, sunflower oil, olive oil, cottonseed oil, rice oil, and safflower oil in the edible oils and fats is preferably 60% by mass or more and 100% by mass or less, more preferably 75% by mass or more and 100% by mass or less, even more preferably 90% by mass or more and 100% by mass or less, and even more preferably 100% by mass. The palm-based oils and fats referred to here mean palm oil and processed palm oil.
食用油脂は、融点が10℃以下であることが好ましく、0℃以下であることがより好ましい。なお、本明細書で、融点は、上昇融点を意味する。上昇融点は、基準油脂分析試験法2.2.4.2-1996に則って測定することができる。Edible fats and oils preferably have a melting point of 10°C or less, and more preferably 0°C or less. In this specification, melting point means the slip melting point. The slip melting point can be measured in accordance with Standard Fats and Oils Analysis Test Method 2.2.4.2-1996.
本発明において用いられる酵素分解レシチンとは、大豆レシチン等の植物レシチンや卵黄レシチンを、ホスホリパーゼ等の酵素で酵素分解して得られる、ホスファチジン酸及びリゾレシチンを主成分とするものであり、液状、ペースト状、粉末状等のいずれの形態のものであっても用いることができるが、液状の形態のものが好ましい。The enzymatically hydrolyzed lecithin used in the present invention is obtained by enzymatically hydrolyzing vegetable lecithin such as soybean lecithin or egg yolk lecithin with an enzyme such as phospholipase, and is composed mainly of phosphatidic acid and lysolecithin. Any form such as liquid, paste, powder, etc. can be used, but the liquid form is preferred.
また、前記酵素分解レシチンは、ホスファチジン酸を主成分とするものが好ましい。前記酵素分解レシチン中のリン脂質に対するホスファチジン酸含量は、50質量%以上100質量%以下であることが好ましく、70質量%以上100質量%以下であることがより好ましく、90質量%以上100質量%以下であることがさらに好ましく、95質量%以上100質量%以下であることがさらにより好ましく、100質量%であることがことさら好ましい。 The enzymatically decomposed lecithin is preferably one containing phosphatidic acid as a main component. The phosphatidic acid content relative to the phospholipid in the enzymatically decomposed lecithin is preferably 50% by mass or more and 100% by mass or less, more preferably 70% by mass or more and 100% by mass or less, even more preferably 90% by mass or more and 100% by mass or less, even more preferably 95% by mass or more and 100% by mass or less, and especially preferably 100% by mass.
また、前記酵素分解レシチン中のリン脂質に対するホスファチジルエタノールアミン含量は、5質量%以下であることが好ましい。 In addition, it is preferable that the phosphatidylethanolamine content relative to the phospholipids in the enzymatically hydrolyzed lecithin is 5% by mass or less.
本発明にかかる離型油においては、酵素分解レシチンをリン脂質として、0.01質量%以上4.5質量%以下含有し、好ましくは0.05質量%以上3質量%以下含有し、より好ましくは0.1質量%以上2.8質量%以下含有し、さらに好ましくは0.1質量%以上2.5質量%以下含有する。多すぎると発煙等に問題が生じる場合がある。The release oil of the present invention contains 0.01% by mass or more and 4.5% by mass or less of enzymatically decomposed lecithin as phospholipid, preferably 0.05% by mass or more and 3% by mass or less, more preferably 0.1% by mass or more and 2.8% by mass or less, and even more preferably 0.1% by mass or more and 2.5% by mass or less. If the amount is too large, problems such as smoke generation may occur.
本発明にかかる離型油には、食用油脂、酵素分解レシチンの他に、通常、食用の油脂組成物に配合される成分を、発明の効果を損なわない範囲において含有していてもよい。例えば、トコフェロール、アスコルビン酸パルミテート、ローズマリー抽出物、茶抽出物、甘草抽出物等の酸化防止剤;クエン酸やリンゴ酸等の金属キレート剤;ビタミンA、ビタミンD等のビタミン類;シリコーン;香料;乳化剤等である。In addition to edible oils and fats and enzymatically decomposed lecithin, the release oil of the present invention may contain components that are usually blended in edible oil and fat compositions, within the range that does not impair the effects of the invention. For example, antioxidants such as tocopherol, ascorbyl palmitate, rosemary extract, tea extract, and licorice extract; metal chelating agents such as citric acid and malic acid; vitamins such as vitamin A and vitamin D; silicone; fragrances; emulsifiers; etc.
本発明にかかる離型油には、酵素分解レシチン以外の乳化剤を含有していてもよい。前記乳化剤としては、酵素分解レシチン以外のレシチン、ポリグリセリン脂肪酸エステル、ポリグリセリン縮合リシノレイン酸エステル、ショ糖脂肪酸エステル、有機酸モノグリセリド、ソルビタン脂肪酸エステル、プロピレングリコール脂肪酸エステル、ポリオキシエチレンソルビタン脂肪酸エステル、ステアロイル乳酸カルシウム等が挙げられる。前記離型油中の酵素分解レシチンを含む乳化剤含有量に対する酵素分解レシチンの含有量の割合が60質量%以上100質量%以下であることが好ましく、70質量%以上100質量%以上であることがより好ましく、90質量%以上100質量%以下であることがさらに好ましく、100質量%であることがさらにより好ましい。The release oil of the present invention may contain an emulsifier other than enzymatically decomposed lecithin. Examples of the emulsifier include lecithin other than enzymatically decomposed lecithin, polyglycerin fatty acid ester, polyglycerin condensed ricinoleic acid ester, sucrose fatty acid ester, organic acid monoglyceride, sorbitan fatty acid ester, propylene glycol fatty acid ester, polyoxyethylene sorbitan fatty acid ester, calcium stearoyl lactate, etc. The ratio of the content of enzymatically decomposed lecithin to the content of emulsifiers including enzymatically decomposed lecithin in the release oil is preferably 60% by mass or more and 100% by mass or less, more preferably 70% by mass or more and 100% by mass or more, even more preferably 90% by mass or more and 100% by mass or less, and even more preferably 100% by mass.
また、前記乳化剤は、ポリグリセリン脂肪酸エステル、ポリグリセリン縮合リシノレイン酸エステル、ショ糖脂肪酸エステル、有機酸モノグリセリド、及びソルビタン脂肪酸エステルから選ばれる1種又は2種以上が好ましく、ポリグリセリン脂肪酸エステル、ポリグリセリン縮合リシノレイン酸エステル、及びソルビタン脂肪酸エステルから選ばれる1種又は2種以上がより好ましく、ポリグリセリン脂肪酸エステルがさらに好ましい。The emulsifier is preferably one or more selected from polyglycerol fatty acid esters, polyglycerol condensed ricinoleic acid esters, sucrose fatty acid esters, organic acid monoglycerides, and sorbitan fatty acid esters, more preferably one or more selected from polyglycerol fatty acid esters, polyglycerol condensed ricinoleic acid esters, and sorbitan fatty acid esters, and even more preferably polyglycerol fatty acid esters.
前記ポリグリセリン脂肪酸エステルは、グリセリン平均重合度が2以上20以下であることが好ましく、2以上16以下であることがより好ましく、6以上12以下であることがさらに好ましく、8以上12以下であることがさらにより好ましい。また、HLBは1.0以上8.0以下が好ましく、2.0以上7.5以下がより好ましく、3.0以上7.0以下がさらに好ましく、4.1以上6.0以下がさらにより好ましい。また、脂肪酸は、オレイン酸、ベヘン酸、及びエルカ酸から選ばれる1種又は2種以上であることが好ましく、オレイン酸であることがより好ましい。The polyglycerol fatty acid ester preferably has an average degree of polymerization of glycerol of 2 to 20, more preferably 2 to 16, even more preferably 6 to 12, and even more preferably 8 to 12. The HLB is preferably 1.0 to 8.0, more preferably 2.0 to 7.5, even more preferably 3.0 to 7.0, and even more preferably 4.1 to 6.0. The fatty acid is preferably one or more selected from oleic acid, behenic acid, and erucic acid, and more preferably oleic acid.
本発明にかかる離型油が適用される食肉加工食品に、特に制限はない。用いられる食肉原料としては、特に制限されず、牛、豚、羊等の家畜の肉、鶏、鴨、家鴨等の家禽類の肉、魚肉等が挙げられる。There is no particular restriction on the processed meat food to which the release oil of the present invention is applied. The meat raw material used is not particularly limited, and includes meat of livestock such as beef, pork, and sheep, poultry such as chicken, duck, and domestic duck, and fish meat.
前記食肉加工食品は、好ましくはひき肉を含む食品である。ひき肉の原料は、特に制限されず、牛、豚、羊等の家畜の肉、鶏、鴨、家鴨等の家禽類の肉、魚肉等であり、好ましくは、牛、豚、鶏から選ばれる1種又は2種以上であり、より好ましくは牛、豚から選ばれる1種又は2種である。特定のひき肉の原料を使うと焦げ付きやすく、本発明の効果が顕著に得られる。The processed meat food is preferably a food containing minced meat. The raw material for the minced meat is not particularly limited and may be meat of livestock such as beef, pork, or lamb, poultry such as chicken, duck, or duck, or fish meat, and is preferably one or more types selected from beef, pork, or chicken, and more preferably one or two types selected from beef and pork. If a specific raw material for minced meat is used, it is prone to burning, and the effects of the present invention can be obtained more remarkably.
また、前記食肉加工食品は、ハンバーグ、肉団子、つくね、ミートローフ、ひき肉炒めなどのひき肉を含む食品が挙げられ、好ましくはハンバーグ、肉団子、つくねであり、より好ましくはハンバーグである。 In addition, the processed meat foods include foods containing minced meat such as hamburger steaks, meatballs, meatloaf, and stir-fried minced meat, preferably hamburger steaks, meatballs, and meatballs, and more preferably hamburger steaks.
また、前記ひき肉炒めの例としては、麻婆豆腐、ナスとひき肉炒め、ガパオライス、ミートソース等が挙げられる。 Examples of stir-fried minced meat include mapo tofu, stir-fried eggplant and minced meat, gapao rice, and meat sauce.
前記食肉加工食品には、食肉以外の植物タンパク質等の食材、調味料、香辛料、香料、保存料、酸味料、増粘剤、ゲル化剤、酸化防止剤等や、タマネギ、ニンジン、ピーマン、キャベツ等の野菜類が含まれてもよい。The processed meat foods may contain ingredients other than meat, such as plant proteins, seasonings, spices, flavorings, preservatives, acidulants, thickeners, gelling agents, antioxidants, etc., and vegetables such as onions, carrots, bell peppers, and cabbage.
一方、本発明にかかる食肉加工食品の製造方法は、前記離型油を加熱調理時に使用する工程を含む。その場合、フライパンや鉄板等で焼成する工程を含むことが好ましい。On the other hand, the method for producing processed meat foods according to the present invention includes a step of using the release oil during cooking. In that case, it is preferable to include a step of baking in a frying pan or on an iron plate.
以下に、本発明の実施例について説明するが、本発明の範囲はこれに限定されるものではない。 The following describes examples of the present invention, but the scope of the present invention is not limited to these examples.
離型油の原料は下記の通りである。
精製菜種油 (株式会社J-オイルミルズ製、上昇融点0℃以下)
酵素分解レシチン1 (ベネコートBMI-40L、リン脂質含量 41.6質量%、ホスファチジン酸含量41.6質量%、ホスファチジルエタノールアミン含量 0質量%、花王株式会社製)
酵素分解レシチン2 (レシマールEL、リン脂質含量 38.2質量%、ホスファチジン酸含量0.76質量%、ホスファチジルエタノールアミン含量 10.1%、理研ビタミン株式会社製)
クルードレシチン (レシチンCL、リン脂質含量 62質量%、ホスファチジン酸含量 9.9質量%、ホスファチジルエタノールアミン含量 18.3%、株式会社J-オイルミルズ製)
分画レシチン (PC-35、リン脂質含量 52.5質量%、ホスファチジン酸含量 0質量%、ホスファチジルエタノールアミン含量 10.0%、株式会社辻製油製)
脱油レシチン (レシチンPW、リン脂質含量 100質量%、ホスファチジン酸含量 11.7質量%、ホスファチジルエタノールアミン含量 29.5%、株式会社J-オイルミルズ製)
ポリグリセリン脂肪酸エステル(Q-175S、HLB4.5、オレイン酸、平均重合度 10、太陽化学株式会社製)
The raw materials for the release oil are as follows:
Refined rapeseed oil (manufactured by J-Oil Mills, Inc., melting point below 0°C)
Enzymatically decomposed lecithin 1 (Benecoat BMI-40L, phospholipid content 41.6% by mass, phosphatidic acid content 41.6% by mass, phosphatidylethanolamine content 0% by mass, manufactured by Kao Corporation)
Enzymatically decomposed lecithin 2 (Resimal EL, phospholipid content 38.2% by mass, phosphatidic acid content 0.76% by mass, phosphatidylethanolamine content 10.1%, manufactured by Riken Vitamin Co., Ltd.)
Crude lecithin (Lecithin CL, phospholipid content 62% by mass, phosphatidic acid content 9.9% by mass, phosphatidylethanolamine content 18.3% by mass, manufactured by J-Oil Mills Co., Ltd.)
Fractionated lecithin (PC-35, phospholipid content 52.5% by mass, phosphatidic acid content 0% by mass, phosphatidylethanolamine content 10.0%, manufactured by Tsuji Oil Mills)
Deoiled lecithin (Lecithin PW, phospholipid content 100% by mass, phosphatidic acid content 11.7% by mass, phosphatidylethanolamine content 29.5%, manufactured by J-Oil Mills Co., Ltd.)
Polyglycerol fatty acid ester (Q-175S, HLB 4.5, oleic acid, average degree of polymerization 10, manufactured by Taiyo Kagaku Co., Ltd.)
なお、レシチンのリン脂質組成及び含量は、以下の方法により測定した。 The phospholipid composition and content of lecithin were measured using the following method.
各レシチンをクロロホルム:メタノール=2:1で希釈したものを下記条件で分析した。
機器:HPLC (Thermo SCIENTIFIC社製)
検出器:荷電化粒子検出器 Corona Veo
移動相: A n-ヘキサン:2-プロパノール:酢酸:トリエチルアミン
=814.2:170:15:0.8 (体積比)
B 2-プロパノール:水:酢酸:トリエチルアミン
=844.2:140:15:0.8 (体積比)
カラム:LiChrospher 100 Diol(5μm) 内径4.0 x 125mm[merck]
カラム温度:55℃
サンプル温度:20℃
グラジエント(流速=1ml/min) ※リニアグラジエント(表1参照)
Each lecithin was diluted with chloroform:methanol=2:1 and analyzed under the following conditions.
Equipment: HPLC (Thermo SCIENTIFIC)
Detector: Corona Veo charged particle detector
Mobile phase: A n-hexane: 2-propanol: acetic acid: triethylamine
= 814.2: 170: 15: 0.8 (volume ratio)
B 2-propanol:water:acetic acid:triethylamine
= 844.2: 140: 15: 0.8 (volume ratio)
Column: LiChrospher 100 Diol (5 μm) inner diameter 4.0 x 125 mm [Merck]
Column temperature: 55°C
Sample temperature: 20°C
Gradient (flow rate = 1 ml/min) *Linear gradient (see Table 1)
クルードレシチンと酵素分解レシチン1を適宜混合したものを日本食品分析センターにてリン脂質類を定量し、これを真の値として標品に用いた。An appropriate mixture of crude lecithin and enzymatically hydrolyzed lecithin 1 was subjected to quantification of phospholipids at the Japan Food Analysis Center, and this was used as the true value as a standard.
<試験例1>
精製菜種油を60℃に保温し、表2に記載した配合でレシチンを5質量%になるように添加して、充分に溶解した後、25℃になるまで放冷して、離型油を得た。
<Test Example 1>
Refined rapeseed oil was kept at 60° C., and lecithin was added to the mixture shown in Table 2 so that the amount was 5% by mass. After the mixture was sufficiently dissolved, the mixture was allowed to cool to 25° C. to obtain a release oil.
得られた離型油について、下記評価方法1で離型性の評価を行った。また、下記評価方法2で着色の評価を行った。得られた評価結果を表2に示す。The release properties of the obtained release oil were evaluated using the following Evaluation Method 1. In addition, coloration was evaluated using the following Evaluation Method 2. The obtained evaluation results are shown in Table 2.
<評価方法1:離型性評価>
A:ハンバーグの調製方法
市販の牛・豚合いびき肉250g、牛乳120mL、ハンバーグヘルパー(ハウス食品株式会社製)46gの割合でよく混合し、120gずつに分け、成形した。
B:離型性の評価方法
1. 直径22cmのステンレス製フライパンの質量を測定した
2. フライパンに離型油10gを入れ、中心の表面温度が200℃になるまでIHヒーターで加熱した
3. 成形したハンバーグ120gをフライパンに乗せて1分間加熱した
4. ハンバーグを裏返し、さらに1分間加熱した
5. フライパンを上下逆にしてハンバーグをフライパンから取り除いた
6. 上記1から5の工程を3回繰り返した
7. ハンバーグを取り除いた後の、フライパンの質量を測定した
8. 上記7で測定した質量と上記1で測定した質量との差を、焦げ付きの質量とした
<Evaluation method 1: Evaluation of releasability>
A: Method for preparing hamburger steak 250 g of commercially available ground beef and pork, 120 mL of milk, and 46 g of Hamburger Helper (manufactured by House Foods Corporation) were thoroughly mixed, divided into 120 g portions, and molded.
B: Method for evaluating releasability 1. The mass of a stainless steel frying pan with a diameter of 22 cm was measured. 2. 10 g of release oil was placed in the frying pan and heated with an IH heater until the surface temperature at the center reached 200°C. 3. 120 g of formed hamburger steak was placed on the frying pan and heated for 1 minute. 4. The hamburger steak was turned over and heated for another minute. 5. The frying pan was turned upside down and the hamburger steak was removed from the frying pan. 6. The above steps 1 to 5 were repeated three times. 7. The mass of the frying pan after the hamburger steak was removed was measured. 8. The difference between the mass measured in step 7 above and the mass measured in step 1 above was taken as the mass of the burnt part.
<評価方法2:着色評価>
A:加熱方法
離型油を16×125mmのガラス試験管に3g採取し、200℃に加熱したオイルバス中で15分間加熱した。
B:吸光度の測定方法
加熱終了後、冷却して520nmの吸光度を測定した。対照として、精製菜種油を用い、必要に応じて精製菜種油で希釈して測定した。加熱前の520nmの吸光度を測定し、加熱後の測定値との差を算出した。吸光度の測定には紫外可視分光光度計(UV-2450;島津製作所社製、1cmアクリル製セル)を用いた。
<Evaluation Method 2: Coloration Evaluation>
A: Heating method 3 g of release oil was placed in a 16×125 mm glass test tube and heated in an oil bath at 200° C. for 15 minutes.
B: Method for measuring absorbance After heating, the sample was cooled and the absorbance at 520 nm was measured. As a control, refined rapeseed oil was used, and the sample was diluted with refined rapeseed oil as necessary. The absorbance at 520 nm was measured before heating, and the difference from the measured value after heating was calculated. A UV-visible spectrophotometer (UV-2450; Shimadzu Corporation, 1 cm acrylic cell) was used to measure the absorbance.
表2に示すように、酵素分解レシチン1、酵素分解レシチン2を用いると焦げ付きの質量が少なく、離型性が高かった。また、酵素分解レシチン1は油脂の着色が非常に少なかった。As shown in Table 2, the amount of burnt matter was small and the release properties were high when enzyme-decomposed lecithin 1 and enzyme-decomposed lecithin 2 were used. Furthermore, enzyme-decomposed lecithin 1 caused very little discoloration of the oil or fat.
<試験例2>
上記試験例1の配合比を表3に示す配合比にした以外は、試験例1と同じ調製方法で、実施例2-1~2-2の離型油を得た。
<Test Example 2>
The release oils of Examples 2-1 and 2-2 were obtained in the same preparation method as in Test Example 1, except that the blending ratio in Test Example 1 was changed to the blending ratio shown in Table 3.
得られた離型油について、前記評価方法1で離型性の評価を行った。得られた試験結果を表3に示す。The release properties of the obtained release oil were evaluated using the above-mentioned Evaluation Method 1. The test results are shown in Table 3.
表3に示すように、酵素分解レシチンの量が0.7質量%(リン脂質含量 0.29質量%)と少ない配合量でも、比較例1-1~1-3に比べて離型性が高いことがわかる。As shown in Table 3, even when the amount of enzymatically hydrolyzed lecithin was as low as 0.7% by mass (phospholipid content: 0.29% by mass), the release property was higher than in Comparative Examples 1-1 to 1-3.
<試験例3>
精製菜種油を60℃に保温し、表4に記載した配合でレシチンとポリグリセリン脂肪酸エステルを添加して、充分に溶解した後、25℃になるまで放冷して、離型油を得た。
<Test Example 3>
Refined rapeseed oil was kept at 60°C, and lecithin and polyglycerol fatty acid ester were added in the proportions shown in Table 4. After fully dissolving, the mixture was allowed to cool to 25°C to obtain a release oil.
得られた離型油について、評価方法3で離型性の評価を行った。得られた試験結果を表4に示す。The release properties of the obtained release oil were evaluated using Evaluation Method 3. The test results are shown in Table 4.
<評価方法3:ハンバーグの離型性評価>
A:ハンバーグの調製方法
市販の牛・豚合いびき肉250g、牛乳120mL、ハンバーグヘルパー(ハウス食品株式会社製)46gの割合でよく混合し、50gずつに分け、成形した。
B:離型性の評価方法
1.直径22cmのステンレス製フライパンの質量を測定した
2.フライパンに離型油10gを入れ、中心の表面温度が200℃になるまでIHヒーターで加熱した
3.成形したハンバーグ50gを、フライパン表面を満遍なく覆うように広げ、1分間加熱した
4.フライパンを上下逆にしてハンバーグを取り除き、質量を測定した
5.上記4で測定した重量と、1で測定した重量との差を、焦げ付きの質量とした
<Evaluation method 3: Evaluation of releasability of hamburger steak>
A: Method for preparing hamburger steak 250 g of commercially available ground beef and pork, 120 mL of milk, and 46 g of Hamburger Helper (manufactured by House Foods Corporation) were thoroughly mixed, divided into 50 g portions, and molded.
B: Method for evaluating releasability 1. The mass of a stainless steel frying pan with a diameter of 22 cm was measured. 2. 10 g of release oil was placed in the frying pan and heated with an IH heater until the surface temperature at the center reached 200°C. 3. 50 g of the formed hamburger steak was spread evenly over the surface of the frying pan and heated for 1 minute. 4. The frying pan was turned upside down, the hamburger steak was removed, and the mass was measured. 5. The difference between the weight measured in 4 above and the weight measured in 1 was taken as the mass of the burnt part.
表4に示すように、酵素分解レシチンとポリグリセリン脂肪酸エステルを含有する離型油を用いると焦げ付きの質量が少なく、離型効果がみられた。
As shown in Table 4, when a release oil containing enzymatically decomposed lecithin and polyglycerol fatty acid ester was used, the amount of burnt matter was small, and a release effect was observed.
Claims (6)
前記離型油は、前記酵素分解レシチンをリン脂質として0.01質量%以上4.5質量%以下含有する、該離型油であり、
前記食肉加工食品は、ハンバーグ、肉団子、つくね、ミートローフ、及びひき肉炒めからなる群から選ばれるひき肉を含む食品である、焦げ付き抑制方法。 A method for preventing burning of processed meat foods, comprising using a release oil obtained by adding enzymatically decomposed lecithin to edible oils and fats for cooking the foods, the method comprising the steps of:
The release oil contains the enzymatically decomposed lecithin in an amount of 0.01% by mass or more and 4.5% by mass or less as a phospholipid,
The processed meat food is a food containing minced meat selected from the group consisting of hamburger steak, meatball, meatball, meatloaf, and stir-fried minced meat .
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| PCT/JP2020/034718 WO2021065444A1 (en) | 2019-09-30 | 2020-09-14 | Mold release oil for processed meat food |
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| Publication number | Priority date | Publication date | Assignee | Title |
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| JP2012249621A (en) | 2011-06-07 | 2012-12-20 | Riken Vitamin Co Ltd | Mold release oil |
| WO2013031332A1 (en) | 2011-08-29 | 2013-03-07 | 株式会社J-オイルミルズ | Oil composition for sautéing and method for producing same |
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| Publication number | Priority date | Publication date | Assignee | Title |
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| JP2012249621A (en) | 2011-06-07 | 2012-12-20 | Riken Vitamin Co Ltd | Mold release oil |
| WO2013031332A1 (en) | 2011-08-29 | 2013-03-07 | 株式会社J-オイルミルズ | Oil composition for sautéing and method for producing same |
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