JPS58162258A - Making method for liquid spice - Google Patents

Making method for liquid spice

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Publication number
JPS58162258A
JPS58162258A JP57044041A JP4404182A JPS58162258A JP S58162258 A JPS58162258 A JP S58162258A JP 57044041 A JP57044041 A JP 57044041A JP 4404182 A JP4404182 A JP 4404182A JP S58162258 A JPS58162258 A JP S58162258A
Authority
JP
Japan
Prior art keywords
oil
chain fatty
fatty acid
medium
spices
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.)
Granted
Application number
JP57044041A
Other languages
Japanese (ja)
Other versions
JPH0115267B2 (en
Inventor
Kenji Hara
健次 原
Kazutomo Maehashi
前橋 和友
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Kao Corp
Original Assignee
Kao Corp
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Kao Corp filed Critical Kao Corp
Priority to JP57044041A priority Critical patent/JPS58162258A/en
Publication of JPS58162258A publication Critical patent/JPS58162258A/en
Publication of JPH0115267B2 publication Critical patent/JPH0115267B2/ja
Granted legal-status Critical Current

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Abstract

PURPOSE:Naturally occurring spices are dipped in a specific middle-sized chain fat oil to extract their useful ingredients to give a liquid spice, thus giving a liquid spice permitting its use for a long period of time, because of its high storage stability. CONSTITUTION:Naturally occurring spices such as peppers, laurel leaves and others are dipped in a middle-sized chain fat oil selected from middle-sized chain fatty acid trigrycerides and triglycerides obtained by partial ester interchange of middle-sized chain fatty acid triglycerides with another food oil to extract their useful ingredients in the form of a liquid spice. The fat oil may contain ethanol, other food oil or water-dispersible emulsifier.

Description

【発明の詳細な説明】 本発明は保存安定性がよく且つ長期使用に耐える液体ス
パイスの製造法に関する。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for producing a liquid spice that has good storage stability and can withstand long-term use.

香辛料(スパイス)は植物の種子、果実、花、樹皮、葉
、根塊などから得られるもので、刺激性の芳香を持ち、
飲食物に香味を与え、食欲を増進したり消化吸収を助け
るものである。香辛料はその使用形態により天然香辛料
と加工香辛料に大別される。天然香辛料は原料植物を乾
燥、粉砕、殺菌して用いるもので、一般的に使用されて
いるが、その成分の逸散速度が速く保存状態が悪いとす
ぐに香辛料としての役目を果たさなくなる。これらの欠
点を改良してさらに食品加工用としても使用できる形態
としたものが加工香辛料である。
Spices are obtained from the seeds, fruits, flowers, bark, leaves, roots, etc. of plants and have a pungent aroma.
It gives flavor to food and drinks, increases appetite, and aids in digestion and absorption. Spices can be broadly classified into natural spices and processed spices depending on the form in which they are used. Natural spices are commonly used by drying, crushing, and sterilizing raw materials from plants, but their components quickly dissipate and if stored in poor storage conditions, they quickly cease to function as spices. Processed spices are products that have improved these drawbacks and have been made into a form that can be used for food processing.

従来、香辛料の有効成分を安定に保持でき、かつ使用し
易い形態の加工香辛料全得んとする多くの研究がなされ
ており、一般に粉末天然香辛料から水蒸気蒸留、溶剤抽
出して得た天然精油、抽出香辛料を種々の形態に加工し
たもの、例えばこれらを乳化、噴霧、乾燥させたコーテ
ィングスパイス;ブドウ糖、食塩、デキス) IJン等
に吸着させた吸着型スパイス;食品添加用界面活性剤と
食用油で乳化した乳化スパイス;アルコール類、植物油
等に溶解した液体スパイス等の加工香辛料が提供されて
いる。
In the past, much research has been conducted to obtain processed spices that can stably retain their active ingredients and are easy to use.In general, natural essential oils obtained by steam distillation and solvent extraction from powdered natural spices, Extracted spices processed into various forms, such as coated spices made by emulsifying, spraying, and drying these; glucose, salt, dextrose, etc.; Adsorption type spices adsorbed on IJ, etc.; surfactants for food additives and edible oils. Processed spices such as emulsified spices and liquid spices dissolved in alcohols, vegetable oils, etc. are provided.

しかしながら、これらの加工香辛料も長期間安定とは言
えず、またその加工素材とじて食用油、植物油を使用し
た場合、放置すると香辛料により油脂が徐々に重合して
、使用している間に次第に粘度が生じ使用不能となるも
のなどもある。例えば、一般家庭、業務用に使用される
辣油(ラー油)は、トウガラシあるいはトウガラシ有効
成分をゴマ油あるいは米糠油に浸漬あるいは溶解させ友
ものであるが、使用している間に次第に粘りが生じ使用
不能になると共にその香辛成分も次第に失われる。
However, these processed spices cannot be said to be stable for a long period of time, and if edible oil or vegetable oil is used as the processed material, if left unattended, the spices will gradually polymerize the oil and fat, and the viscosity will gradually increase during use. There are some that occur and become unusable. For example, chili oil (chili oil) used for general household and commercial purposes is made by soaking or dissolving chili peppers or the active ingredients of chili peppers in sesame oil or rice bran oil, but it gradually becomes sticky during use and becomes unusable. As it ages, its spicy ingredients are gradually lost.

そこで、本発明者は上記欠点を改善すべく鋭意研究を行
った結果、天然香辛料全特定の脂肪油で抽出すると香辛
成分の損失が少なく、しかもその抽出物は使用中粘度の
増加が起らず長期間安定に使用ないし保存できることを
 3− 見出し、本発明を完成した。
Therefore, the present inventor conducted intensive research to improve the above drawbacks and found that when natural spices are extracted with a specific fatty oil, there is less loss of spice components, and the extract does not increase in viscosity during use. 3- They discovered that it can be used or stored stably for a long period of time, and completed the present invention.

すなわち、本発明は、天然香辛料を、中鎖脂肪酸トリグ
リセライド及び中鎖脂肪酸トリグリセ2イドを他の食用
油で部分的にエステル交換したトリグリセライドよりn
る群から選ばれた中鎖脂肪油に浸漬し、その有効成分を
抽出して液体スパイスを製造する方法である。
That is, the present invention provides natural spices with a medium-chain fatty acid triglyceride and a medium-chain fatty acid triglyceride partially transesterified with other edible oils.
This is a method to produce liquid spices by soaking them in medium-chain fatty oil selected from the group of 100% to 100% and extracting their active ingredients.

本発明で原料として使用される天然香辛料としては、例
えば百味コシヨウ、月桂葉、カルク、ショウズク、桂皮
、トウガラシ、丁子、コエンドロ、マキノ、キヨウオウ
、イノンド、ウィキョウ、ショウガ、西洋ワサビ、トシ
ョウシ、ニクズク、マヨラナ、西洋カフシ、赤トウガラ
シ、コシヨウ、ハツカ、サフラン、 4− セージ、セーヴオリー、タイム、ウコン、ヴアニラ、ア
ニス、オニオン、ニンニク、カルダモン、キャラウェー
、クミン、コリアンダー、ナツメグ、メース、パプリカ
等が挙げられる。
Examples of natural spices used as raw materials in the present invention include cilantro, bay leaf, calc, shizuku, cinnamon, chili pepper, clove, cilantro, makino, chili pepper, dill, fennel, ginger, horseradish, toshoshi, nikuzuku, and marjoram. , Western kafshi, red chili pepper, koshiyo, pepper, saffron, 4- sage, save oli, thyme, turmeric, vinilla, anise, onion, garlic, cardamom, caraway, cumin, coriander, nutmeg, mace, paprika and the like.

これらは材料植物そのものも使用できるが、一般には細
切又は粉末化したものが好ましく、更にこれらから得ら
れる精油あるいは抽出物を使用することもできる。
Although these plants can be used as raw materials, it is generally preferable to use shredded or powdered plants, and essential oils or extracts obtained from these plants can also be used.

本発明において、中鎖脂肪酸トリグリセライドとしては
、通常その構成脂肪酸が炭素数6〜10の飽和脂肪酸を
90%以上含有するものが使用され、一般にはヤシ油等
から得ることができる。
In the present invention, the medium-chain fatty acid triglyceride used is one whose constituent fatty acids contain 90% or more of saturated fatty acids having 6 to 10 carbon atoms, and can generally be obtained from coconut oil or the like.

また、中鎖脂肪酸トリグリセライドを部分的にエステル
交換するために使用される食用油は、炭素数12以上の
長鎖脂肪酸トリグリセライドを主成分とするもので、例
えばパーム油、牛脂、豚油、大豆油、小麦胚芽油、オリ
ーブ油、落花生油、米糠油、ゴマ油、ナタネ油等が挙げ
られる。このエステル交換は2mあるいはそれ以上の油
脂の混合物をアルカリ触謀の下で加熱する周知の方法に
より行なわれる。その際の混合比(重量)の範囲は、そ
のエステル交換油の特性を考慮して、中鎖脂肪酸トリグ
リセライドに対して他の食用油を2倍量まで、好ましく
は1/!倍量まで用いるのが良い。
In addition, the edible oils used to partially transesterify medium-chain fatty acid triglycerides are those whose main components are long-chain fatty acid triglycerides with 12 or more carbon atoms, such as palm oil, beef tallow, pork oil, and soybean oil. , wheat germ oil, olive oil, peanut oil, rice bran oil, sesame oil, rapeseed oil and the like. This transesterification is carried out by the well-known method of heating a mixture of 2m or more fats and oils under alkaline catalysis. In this case, the range of the mixing ratio (weight) should be up to 2 times the amount of other edible oil to medium chain fatty acid triglyceride, preferably 1/! It is best to use up to double the amount.

本発明方法を実施するには、天然香辛料を上記中鎖脂肪
油に浸漬して有効成分を抽出する。浸漬抽出は室温〜1
50℃、特に室温〜100℃の温度で行うのが好ましく
、抽出時間は特に制限されない。また、中鎖脂肪油の量
は天然香辛料に対して等量〜100倍(重量)、特に2
〜50倍が好ましい。
To carry out the method of the present invention, natural spices are soaked in the medium-chain fatty oil described above to extract the active ingredients. Immersion extraction at room temperature ~1
It is preferable to carry out the extraction at a temperature of 50°C, particularly room temperature to 100°C, and the extraction time is not particularly limited. In addition, the amount of medium-chain fatty oil should be equal to or 100 times (by weight) the amount of natural spices, especially 2
~50 times is preferred.

また、天然香辛料の中には加熱処理によって特有の香味
をもたらすものがあり、例えばいりゴマ、ニンニクの焦
げ風味は独特のものであるが、このような場合には、予
め細分化した香辛料と中鎖脂肪酸トリグリセライドとを
加熱するか、あるいは少量の食用油と混合して加熱して
風味を醸成したのち、中鎖脂肪油に浸漬することによっ
て、香味の蒸散を最小限に止めることができるとと本に
、場合によっては食用油の加熱後の風味や香味を助長す
る効果がある。
In addition, some natural spices develop a unique flavor through heat treatment, such as the unique burnt flavor of roasted sesame seeds and garlic. It is believed that evaporation of flavor can be minimized by heating chain fatty acid triglycerides or by heating the mixture with a small amount of edible oil to develop flavor, and then immersing it in medium-chain fatty oil. In some cases, it has the effect of enhancing the flavor and aroma of cooking oil after heating.

 7− 更に、本発明において、上記中鎖脂肪油にエタノールを
添加したものを使用すると、抽出時間及び抽出率が改善
される。また、中鎖脂肪油には他の食用油、例えばオリ
ーブ油、落花生油、米糠油、ゴマ油、ナタネ油、その他
元来独特の香味をもって調理に賞月される食用油を適量
配合することもできる。これは他の食用油の風味を附加
して用いる場合に好都合である。
7- Furthermore, in the present invention, when the above-mentioned medium-chain fatty oil to which ethanol is added is used, the extraction time and extraction rate are improved. In addition, appropriate amounts of other edible oils such as olive oil, peanut oil, rice bran oil, sesame oil, rapeseed oil, and other edible oils that have a unique flavor and are used in cooking can also be blended with the medium-chain fatty oil. This is advantageous when using other edible oils with added flavor.

更Kまた、中鎖脂肪油はその固有の粘度によって水相へ
の分散性は食用油よりはるかに優れているが、これに少
量の水分散性乳化剤を添加すると、その水相への分散性
が更に容易となり、スパイスとしての効果が一層高めら
れる。ここで使用される水分散性乳化剤と 8− しては、それ自身が水に分散可能であり、且つ油脂に可
溶のもので、例えばレシチン、ショ糖脂肪酸エステル、
モノグリセライド及びその有機酸エステル(乳酸、コハ
ク酸、酒石酸等)、ポリグリセリン脂肪酸エステル、ソ
ルビタン脂肪酸エステル、ポリオキシエチレンモノグリ
セリド、ポリオキシエチレンソルビタン脂肪酸エステル
などの可食性乳化剤が挙げられる。水分散性乳化剤の中
鎖脂肪油への添加量は、中鎖脂肪油及び当該乳化剤の種
類によって異なるが、本製品を食品に添加した場合の乳
化剤の呈する風味あるいは分散性を考慮すると、一般に
後者に対し前者を0.05〜5重量%、特に0.1〜3
重量%添加するのが好ましい。
Additionally, due to its inherent viscosity, medium-chain fatty oils have much better dispersibility in the aqueous phase than edible oils, but adding a small amount of water-dispersible emulsifier to them improves their dispersibility in the aqueous phase. It becomes even easier to use, and the effect as a spice is further enhanced. The water-dispersible emulsifier used here is one that is itself dispersible in water and soluble in fats and oils, such as lecithin, sucrose fatty acid ester,
Edible emulsifiers include monoglyceride and its organic acid ester (lactic acid, succinic acid, tartaric acid, etc.), polyglycerin fatty acid ester, sorbitan fatty acid ester, polyoxyethylene monoglyceride, polyoxyethylene sorbitan fatty acid ester, and the like. The amount of water-dispersible emulsifier added to medium-chain fatty oil varies depending on the type of medium-chain fatty oil and the emulsifier, but considering the flavor or dispersibility of the emulsifier when this product is added to food, it is generally the latter. 0.05 to 5% by weight of the former, especially 0.1 to 3% by weight
It is preferable to add % by weight.

次に実施例及び参考例を挙げて、一本発明を更に詳細に
説明する。
Next, the present invention will be explained in more detail by giving examples and reference examples.

実施例1 精製中鎖脂肪酸トリグリセライド(化工7−ド■製:商
品名ココナートRK:脂肪酸組成;カプロン酸 0.5
%、カプリル酸 973%。
Example 1 Purified medium chain fatty acid triglyceride (manufactured by Kako 7-do ■: trade name Coconat RK: fatty acid composition; caproic acid 0.5
%, caprylic acid 973%.

カブリン酸 2.21 ) 950 Fに99.91−
Zタ−メリックを添加し、さらに300fの赤トウガラ
シ粉末を添加する。ゆるやかに攪拌しながら5時間放置
後、濾過し、赤トウガラシ粉末を除去する。さらに減圧
下エタノールを除去し、疎油920ffk得る。この疎
油は室温で30日間開栓のまま放置しても流動性は全く
変化しなかった。
Cabric acid 2.21) 99.91- at 950 F
Add Z turmeric and further add 300f red chili powder. After standing for 5 hours with gentle stirring, filter to remove red chili powder. Further, ethanol is removed under reduced pressure to obtain 920ffk of lipophobicity. Even when this oleophobic product was left open for 30 days at room temperature, the fluidity did not change at all.

比較例1゜ 実施例1の中鎖脂肪酸トリグリセライドをゴマ油に代え
て同様な操作を行ない調製した疎油け、室温lO日間開
栓放置で粘シを生じ使用に耐えられなくなった。
Comparative Example 1 An oleophobic soap prepared in the same manner as in Example 1 except that the medium-chain fatty acid triglyceride was replaced with sesame oil became sticky and unusable after being left open for 10 days at room temperature.

実施例2゜ 実施例1の疎油に309のゴマ油を添加し、香シ、風味
の良い疎油を得る。この疎油も室温で30日間開栓のま
ま放置しても流動性はほとんど変化しなかった。
Example 2 Sesame oil No. 309 was added to the oleophobic substance of Example 1 to obtain an oleophobic substance with good aroma and flavor. Even when this oleophobic bottle was left open for 30 days at room temperature, the fluidity hardly changed.

実施例3゜ 精製中鎖脂肪酸トリグリセライド(実施例1で使用した
ものに同じ)と、ゴマ油を重量比で、10:1の割合で
エステル交換させ得たトリグリセライドを用い、実施例
1と同様の操作を行なう。
Example 3: The same procedure as in Example 1 was carried out using purified medium-chain fatty acid triglyceride (same as that used in Example 1) and triglyceride obtained by transesterifying sesame oil at a weight ratio of 10:1. Do the following.

11− この疎油も室温で30日間開栓のまま放置しても流動性
はほとんど変化しなかった。
11- Even when this oleophobic product was left open for 30 days at room temperature, the fluidity hardly changed.

実施例4゜ 中鎖脂肪酸トリグリセライド(実施例1で使用したもの
に同じ)IKPf:100〜110℃に加熱し、これに
オールスパイス8?、トウガラン10t1コリアンダー
フ2t1クミン201.ジンジャ−1Of1フエネグリ
ーク20t1黒コシヨウ10t1マスタード10へター
メリック401の各粉末混合物を投入攪拌し、水分の蒸
散を終えた後、室温に放置して香味の熟成を待って戸別
し、カレー風味の組成物を得る。
Example 4 Medium chain fatty acid triglyceride (same as that used in Example 1) IKPf: Heated to 100-110°C, and added allspice 8? , chili pepper 10t1 coriander hut 2t1 cumin 201. Ginger 1 of 1 Fenugreek 20 t 1 Black pepper 10 t 1 Mustard 10 Add each powder mixture of turmeric 401 and stir.After evaporation of water, leave it at room temperature to wait for the flavor to ripen, then go door to door to make a curry flavored composition. obtain.

実施例& 中鎖脂肪酸トリグリセライド(実施例1で12− 使用したものに同じ)100Fを約150℃に加熱し、
これに細断したショウガ200fを投入攪拌する。水分
が蒸散しショウガがやや褐色化したところで加熱を中止
し、冷却後、中鎖脂肪酸トリグリセライド400tを追
加攪拌し、ショウガを炉別してショウガ風味組成物を得
る。また最初に鶏肉脂肪100tを加熱してショウガを
投入し、以後同様にして組成物を得る。
Example & Medium chain fatty acid triglyceride (same as that used in Example 1) 100F was heated to about 150℃,
Add 200f of shredded ginger to this and stir. When the water evaporates and the ginger turns slightly brown, heating is stopped, and after cooling, 400 t of medium-chain fatty acid triglyceride is added and stirred, and the ginger is separated in a furnace to obtain a ginger-flavored composition. First, 100 tons of chicken fat is heated, ginger is added, and a composition is obtained in the same manner.

実施例6゜ ラード100ft−炒め鍋で加熱し、玉ネギ、ニンニク
(4対1)のみじん切fi3QOfを投入し、全体が暗
褐色化するまで炒める。冷却後中鎖脂肪酸トリグリセラ
イド(実施例1で使用したものに同じ)400ftl−
加えて攪拌し、放置後、固型物を炉別して組成物を得る
Example 6: Heat lard in a 100ft frying pan, add chopped onions and garlic (4:1 ratio), and stir-fry until the whole lard turns dark brown. After cooling, 400 ftl of medium chain fatty acid triglyceride (same as that used in Example 1)
After addition, the mixture is stirred and left to stand, and then the solid matter is separated in a furnace to obtain a composition.

実施例7゜ 実施例1の疎油にポリオキシエチレン・ソルビタンモノ
オレート(化工アトラス株製:ツイーン80)を3チ添
加すると、醤油あるいは食酢に添加した場合にすみやか
に混ざシ合う自己乳化型の疎油ができる。
Example 7゜When 3 g of polyoxyethylene sorbitan monooleate (manufactured by Kako Atlas Co., Ltd.: Tween 80) is added to the oleophobic compound of Example 1, it becomes a self-emulsifying type that quickly mixes when added to soy sauce or vinegar. oleophobicity is formed.

実施例8゜ 実施例4.の組成物を作る際、冷却後追加する中鎖脂肪
酸トリグリセライドに大豆レシチン10t1ソルビタン
脂肪酸エステル(化工アトラス■製;スパン6G)50
f’i加えて水分散性の組成物を得る。
Example 8゜Example 4. When making the composition, add soybean lecithin 10t1 sorbitan fatty acid ester (manufactured by Kako Atlas ■; Span 6G) 50% to the medium chain fatty acid triglyceride that is added after cooling.
f'i to obtain a water-dispersible composition.

以上 15− 367−that's all 15- 367-

Claims (1)

【特許請求の範囲】 1、 天然香辛料を、中鎖脂肪酸トリグリセライド及び
中鎖脂肪酸トリグリセライドを他の食用油で部分的にエ
ステル交換したトリグリセライドよりなる群から選ばれ
た中鎖脂肪油に浸漬し、その有効成分を抽出することを
特徴とする液体スパイスの製造法。 2、 天然香辛料が、予め中鎖脂肪油又は食用油と加熱
処理されたものである特許請求の範囲第1項記載の製造
法。 & 中鎖脂肪油がエタノール、他の食用油又は水分散性
乳化剤を含むものである%Pff−請求の範囲第1項記
載の製造法。
[Claims] 1. Natural spices are immersed in a medium-chain fatty acid oil selected from the group consisting of medium-chain fatty acid triglycerides and triglycerides obtained by partially transesterifying medium-chain fatty acid triglycerides with other edible oils. A method for producing liquid spices characterized by extracting active ingredients. 2. The manufacturing method according to claim 1, wherein the natural spice is previously heat-treated with medium-chain fatty oil or edible oil. & %Pff, wherein the medium-chain fatty oil contains ethanol, other edible oil, or a water-dispersible emulsifier - The method according to claim 1.
JP57044041A 1982-03-19 1982-03-19 Making method for liquid spice Granted JPS58162258A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP57044041A JPS58162258A (en) 1982-03-19 1982-03-19 Making method for liquid spice

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP57044041A JPS58162258A (en) 1982-03-19 1982-03-19 Making method for liquid spice

Publications (2)

Publication Number Publication Date
JPS58162258A true JPS58162258A (en) 1983-09-26
JPH0115267B2 JPH0115267B2 (en) 1989-03-16

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Country Link
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Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS62262967A (en) * 1986-05-09 1987-11-16 Kao Corp Spice
EP0639336A1 (en) * 1993-08-17 1995-02-22 Societe Des Produits Nestle S.A. Process for extracting antioxydants of vegetable origin as liquids
JPH07308170A (en) * 1994-05-18 1995-11-28 Shinguru Seru Shokuhin Kk Food improved in antimutagenic titer
WO1996032024A1 (en) * 1995-04-13 1996-10-17 Pet Incorporated Method for removal of capsaicinoids from peppers
JP2010029083A (en) * 2008-07-28 2010-02-12 Soda Aromatic Co Ltd Method for producing flavor extract
JP2016174550A (en) * 2015-03-19 2016-10-06 日清オイリオグループ株式会社 Edible oil
JP6490289B1 (en) * 2018-04-27 2019-03-27 日本水産株式会社 How to protect the aroma of aqueous food
JP2020029492A (en) * 2018-08-21 2020-02-27 国立大学法人北海道大学 Method for efficiently extracting lipophilic functional component by edible oil

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS575665A (en) * 1980-05-14 1982-01-12 Cpc International Inc Production of flavor concentrate
JPS642345A (en) * 1987-06-24 1989-01-06 Fujitsu Ltd Semiconductor integrated circuit device

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS575665A (en) * 1980-05-14 1982-01-12 Cpc International Inc Production of flavor concentrate
JPS642345A (en) * 1987-06-24 1989-01-06 Fujitsu Ltd Semiconductor integrated circuit device

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS62262967A (en) * 1986-05-09 1987-11-16 Kao Corp Spice
EP0639336A1 (en) * 1993-08-17 1995-02-22 Societe Des Produits Nestle S.A. Process for extracting antioxydants of vegetable origin as liquids
JPH07308170A (en) * 1994-05-18 1995-11-28 Shinguru Seru Shokuhin Kk Food improved in antimutagenic titer
WO1996032024A1 (en) * 1995-04-13 1996-10-17 Pet Incorporated Method for removal of capsaicinoids from peppers
JP2010029083A (en) * 2008-07-28 2010-02-12 Soda Aromatic Co Ltd Method for producing flavor extract
JP2016174550A (en) * 2015-03-19 2016-10-06 日清オイリオグループ株式会社 Edible oil
JP6490289B1 (en) * 2018-04-27 2019-03-27 日本水産株式会社 How to protect the aroma of aqueous food
JP2019193615A (en) * 2018-04-27 2019-11-07 日本水産株式会社 Method for protecting aroma of aqueous food
JP2020029492A (en) * 2018-08-21 2020-02-27 国立大学法人北海道大学 Method for efficiently extracting lipophilic functional component by edible oil

Also Published As

Publication number Publication date
JPH0115267B2 (en) 1989-03-16

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