JPS608277B2 - vegetable high stability oil - Google Patents

vegetable high stability oil

Info

Publication number
JPS608277B2
JPS608277B2 JP6257381A JP6257381A JPS608277B2 JP S608277 B2 JPS608277 B2 JP S608277B2 JP 6257381 A JP6257381 A JP 6257381A JP 6257381 A JP6257381 A JP 6257381A JP S608277 B2 JPS608277 B2 JP S608277B2
Authority
JP
Japan
Prior art keywords
oil
macadamia nut
stability
acid
added
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
Application number
JP6257381A
Other languages
Japanese (ja)
Other versions
JPS57179297A (en
Inventor
晴雄 吉永
正七郎 川嶋
恒夫 鎌田
節也 藤田
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.)
NIPPON YUSHI KK
SEBUN TETSUKU KK
Original Assignee
NIPPON YUSHI KK
SEBUN TETSUKU KK
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 NIPPON YUSHI KK, SEBUN TETSUKU KK filed Critical NIPPON YUSHI KK
Priority to JP6257381A priority Critical patent/JPS608277B2/en
Publication of JPS57179297A publication Critical patent/JPS57179297A/en
Publication of JPS608277B2 publication Critical patent/JPS608277B2/en
Expired legal-status Critical Current

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  • Fats And Perfumes (AREA)

Description

【発明の詳細な説明】 本発明は構成脂肪酸の7〜45重量%(以下%は重量%
を示す)がへキサデセン酸である植物性高安定性油に関
するものであり、さらに詳しくは、マカダミァナッッ油
、にトコフェロールを添加してなるAOM安定度が10
畑時間以上の液体植物性高安定性油に関するものである
DETAILED DESCRIPTION OF THE INVENTION The present invention uses 7 to 45% by weight of the constituent fatty acids (hereinafter % means % by weight).
This article relates to a highly stable vegetable oil in which hexadenoic acid (indicating 1) is hexadecenoic acid.
It concerns a liquid vegetable highly stable oil that lasts more than field time.

液体植物性は、流動性、均一性、潤滑性、可食性などの
特性を有しおり、食品分野に利用されているばかりでは
なく、化粧品用油脂、薬用油脂、潤滑油、無揮発性溶剤
などの基剤としても重要であり、広く利用されている。
Liquid vegetable oils have properties such as fluidity, uniformity, lubricity, and edibility, and are used not only in the food field, but also in cosmetic oils, medicinal oils, lubricating oils, non-volatile solvents, etc. It is also important as a base and is widely used.

一般に液体油はリノール酸、リノレン酸等の多不飽和脂
肪酸を多く含有するために酸化安定性が悪く、臭い、ベ
トッキ、味の低下など劣イ8現象が起りやすいという欠
点を有しており、前記用途に使用する場合、必ずしも品
質的に満足されるものではなく、むしろ大きな障害とな
っており、酸化安定性の高い潤滑性の良い液体油の開発
が強く望まれてし、た。本発明者らは、マカダミアナツ
ツ油が構成脂肪酸中の多不飽和脂肪酸が少なく、かつ、
凝固点の低いことに着目し、これを高安定性油に利用す
る研究を続けた。
In general, liquid oils contain a large amount of polyunsaturated fatty acids such as linoleic acid and linolenic acid, so they have poor oxidation stability and have the disadvantage of being prone to poor 8 phenomena such as odor, stickiness, and decreased taste. When used in the above-mentioned applications, the quality is not necessarily satisfactory, but rather poses a major obstacle, and there has been a strong desire to develop a liquid oil with high oxidation stability and good lubricity. The present inventors discovered that macadamia nut oil has a low content of polyunsaturated fatty acids in its constituent fatty acids, and
Focusing on the low freezing point, he continued research to utilize this in highly stable oils.

マカダミアナッッ油は、豪州(原産地)、ハワイ(主産
地)、南アフリカケニャなどで産出するマカダミアナツ
ッから圧搾などの処理により得られる液体植物油であり
、その構成脂肪酸を分析例で示すと、ミリスチン酸0.
9%、バルミチン酸8.3%、ヘキサデセン酸23.8
%、ステアリン酸2.8%、オレイン酸57.2%、リ
ノール酸1.8%、アラキジン酸2.2%、ェィコセン
酸2.2%、べへニン酸0.7%であり、ヘキサデセン
酸を特異的に多く含んでいる。
Macadamia nut oil is a liquid vegetable oil obtained through processing such as pressing from macadamia nuts produced in Australia (origin), Hawaii (main production area), and Kenya, South Africa. ..
9%, valmitic acid 8.3%, hexadecenoic acid 23.8%
%, stearic acid 2.8%, oleic acid 57.2%, linoleic acid 1.8%, arachidic acid 2.2%, eicosenoic acid 2.2%, behenic acid 0.7%, and hexadecenoic acid. Contains a uniquely large amount of.

このマカダミアナツツ油は、脂肪酸組成からジェン酸以
上の不飽和酸が少ないので、酸化安定性が非常に良いと
考えられたが、AOM安定度は30〜5q時間であり、
一般のサラダ油等の3〜5倍良いという程度であり、脂
肪酸組成から推定されるAOM安定度(約12畑時間)
よりはるかに低かった。
This macadamia nut oil was thought to have very good oxidation stability because its fatty acid composition contained few unsaturated acids higher than genic acid, but the AOM stability was 30 to 5 q hours.
It is 3 to 5 times better than general salad oil, etc., and the AOM stability estimated from the fatty acid composition (about 12 field hours)
It was much lower than that.

我々は、さらに鋭意研究の結果、マカダミアナツッ油の
トコフェロール含量が異常に少ないことを発見し、マカ
ダミアナッッ油のように構成脂肪酸中にへキサデセン酸
を多く含有する油脂にトコフェロールを適量加えること
により安定性が従来の植物油及び油脂技術では全く考え
られないほど飛躍的に向上するとの知見を得、本発明を
完成させたものである。
As a result of further intensive research, we discovered that the tocopherol content of macadamia nut oil is abnormally low, and by adding an appropriate amount of tocopherol to oils and fats such as macadamia nut oil, which contain a large amount of hexadecenoic acid in their constituent fatty acids, we have stabilized the tocopherol content. The present invention was completed based on the knowledge that the properties of oil and oil can be dramatically improved to an extent unimaginable with conventional vegetable oil and fat technology.

すなわち、本発明は、構成脂肪酸の7〜45重量%がへ
キサデセン酸となるようにマカダミアナッッ油を含有す
る液体油にトコフェロールを0.002〜0.2%含有
させてなるAOM安定度100時間以上の植物性高安定
性油に関するものである。
That is, the present invention provides an AOM stability for 100 hours in which a liquid oil containing macadamia nut oil contains 0.002 to 0.2% tocopherol so that 7 to 45% by weight of the constituent fatty acids are hexadecenoic acid. The present invention relates to the above highly stable vegetable oil.

本発明に使用する油脂としてマカダミアナツツ油または
これを所定量配合した液体油がある。
The oils and fats used in the present invention include macadamia nut oil or liquid oil containing a predetermined amount of macadamia nut oil.

マカダミアナッッ油は、その構成脂肪酸中にへキサデセ
ン酸を20%以上と特異的に多く含有しているが、トコ
フェロールなどの酸化防止剤は0.001%以下と著し
く少なく、他の植物油の100ないし数百分の1しか含
有していない。本発明に使用するマカダミアナッッ油は
、マカダミアナッッから圧搾または溶剤抽出によって得
られるもののどちらでも長いが、圧搾法で得られるマカ
ダミアナッッ油は色調が良好である。
Macadamia nut oil has a uniquely high content of hexadecenoic acid (more than 20%) in its constituent fatty acids, but antioxidants such as tocopherols are extremely low at less than 0.001%, which is 100% or more than other vegetable oils. It contains only a few hundredths of a percent. The macadamia nut oil used in the present invention can be obtained from macadamia nut by pressing or solvent extraction, but macadamia nut oil obtained by the pressing method has a good color tone.

これらのマカダミアナッッ油は、必要に応じ精製をおこ
なうが、吸着剤による軽い脱色処理と常法による脱臭処
理により、ほとんど無色、無味、無臭、凝固点−1〆○
以下の清澄な液体油となる。また、本発明に使用する油
脂としては、マカダミアナツツ油を他の液体油たとえば
大豆油、コーン油、菜種油、落花生油、綿実油、米油、
MCT(中鎖糞肪酸トリグリセリド)などと混合して、
構成脂肪酸中のへキサデセン酸が7%〜45%になるよ
うにしたものも使用できる。その他に、あらかじめ分別
して得たへキサデセン酸のグリセリドを他の液体油に所
定量配合した油脂を使用してもよい。構成脂肪酸中のへ
キサデセン酸の量が7%未満のもので液体性のよい高安
定性油を得ることができない。
These macadamia nut oils are purified as necessary, but are almost colorless, tasteless, odorless, and have a freezing point of -1.
The following clear liquid oil is obtained. In addition, the oils and fats used in the present invention include macadamia nut oil, other liquid oils such as soybean oil, corn oil, rapeseed oil, peanut oil, cottonseed oil, rice oil,
Mixed with MCT (medium chain fatty acid triglyceride) etc.
It is also possible to use one in which the hexadecenoic acid content in the constituent fatty acids is 7% to 45%. In addition, an oil or fat obtained by blending a predetermined amount of hexadecenoic acid glyceride obtained by pre-fractionation with another liquid oil may also be used. If the amount of hexadecenoic acid in the constituent fatty acids is less than 7%, a highly stable oil with good liquid properties cannot be obtained.

トコフェロールの含有量は、油脂中濃度0.002〜0
.2%が好ましい。
The content of tocopherol in fats and oils is 0.002 to 0.
.. 2% is preferred.

この含有量が0.002%未満では安定性の向上効果が
小さく、0.2%を越えてもその効果は増大せず、他の
面で不都合が生じて好ましくない。本発明においては、
上記のトコフェロールを油脂に直接添加するか、あるい
はトコフェロール含量がマカダミアナッッ油の約10ぴ
音である他の植物油、たとえば、大豆油、コーン油、菜
種油、落花生油、線葵油、米油などを油脂に配合して、
トコフェロールを所定量含有させることができる。他の
植物油を配合する場合、マカダミアナッッ油に対してそ
の配合量を多くし過ぎると、構成脂肪酸中のへキサデセ
ン酸の量が前記範囲を外れるおそれがあるので、マカダ
ミアナツツ油の量を30%以上、特に好ましくは50%
以上にすることが望ましい。本発明においてトコフェロ
ールを添加後の油脂の安定性は、無添加油の数倍以上と
著しく向上し、これは構成脂肪酸中にへキサデセン酸を
特異的に多く含有するマカダミアナッッ油特有の現象で
あり、オレィン酸主体の他の液体油では見られないこと
である。
If this content is less than 0.002%, the effect of improving stability will be small, and if it exceeds 0.2%, the effect will not increase and other problems will occur, which is not preferable. In the present invention,
The above-mentioned tocopherols can be added directly to the oil or fat, or other vegetable oils with a tocopherol content about 10 pm higher than macadamia nut oil, such as soybean oil, corn oil, rapeseed oil, peanut oil, hollyhock oil, rice oil, etc. Mixed with oil and fat,
A predetermined amount of tocopherol can be contained. When blending other vegetable oils, if the blending amount is too large compared to macadamia nut oil, the amount of hexadecenoic acid in the constituent fatty acids may be out of the above range, so the amount of macadamia nut oil should be reduced by 30%. or more, particularly preferably 50%
It is desirable to do more than that. In the present invention, the stability of oils and fats after adding tocopherol is significantly improved to several times that of oil without additives, and this is a phenomenon unique to macadamia nut oil, which specifically contains a large amount of hexadecenoic acid in its constituent fatty acids. This is something that cannot be seen with other liquid oils based on oleic acid.

たとえば、トコフェロール無添加のマカダミアナツッ油
(AOM安定度4畑時)にトコフェロールを約0.02
%添加すると、AOM安定度は、約400時間を示し、
超高安定性油となる。本発明の植物性高安定性油は、高
安定性、液体性、無臭性などが特に要求される化粧品用
油脂、薬用油脂、フレーバーなどの溶剤、精密機械およ
び食品用機械の潤滑剤、食品加工用油脂などの種々の用
途に適するものである。
For example, tocopherol-free macadamia nut oil (AOM stability level 4 field) contains about 0.02 tocopherols.
% addition, the AOM stability shows approximately 400 hours;
It becomes an ultra-high stability oil. The highly stable vegetable oil of the present invention can be used as a solvent for cosmetics, medicinal oils, flavorings, etc., which particularly require high stability, liquidity, and odorlessness, lubricants for precision machinery and food processing machines, and food processing machines. It is suitable for various uses such as industrial oils and fats.

次に本発明の実施例および応用例を示す。Next, examples and application examples of the present invention will be shown.

実施例 1 マカダミアナッッ油を圧搾抽出して得た油を24時間静
鷹し、水分とオリをデカンタ−により除去し、さらに炉
過をおこない清澄なマカダミアナッツ油を得た。
Example 1 The oil obtained by compressing and extracting macadamia nut oil was left to stand still for 24 hours, water and sludge were removed using a decanter, and the oil was filtered in an oven to obtain clear macadamia nut oil.

このマカダミアナツッ油の総トコフェロールは0.00
042%であり、構成脂肪酸中のへキサデセン酸は23
.8%であった。これに酸化防止剤としては市販のトコ
フェロール(純度98%)をそれぞれ0.001%、0
.002%、0.005%、0.002%、添加し、未
添加油とともにAOM安定度(A.0.C.S.Ten
tative,Me比odによる)を測定し、計算され
たトコフェロールの含有量と対比した結果を第1表に示
す。トコフェロールを0.002%以上含有させたもの
は、この表から明らかなように安定性が顕著に向上して
いた。第1表実施例 2 実施例1で得られた清澄なマカダミアナッッ油(トコフ
ェロール無添加のもの)に袴製コ−ン油(トコフェロー
ル含有量0.09240%)を1%、2%、3%、10
%配合したものをそれぞれ調製し、マカダミアナッッ油
、精製コーンとともにAOM安定度を測定した結果をト
コフヱロール含有量とともに第2表に示した。
The total tocopherol content of this macadamia nut oil is 0.00.
042%, and hexadecenoic acid in the constituent fatty acids is 23%.
.. It was 8%. In addition, commercially available tocopherol (purity 98%) was added as an antioxidant at 0.001% and 0.00%, respectively.
.. 002%, 0.005%, 0.002%, AOM stability (A.0.C.S.Ten
tative, Me ratio od) was measured and compared with the calculated tocopherol content, the results are shown in Table 1. As is clear from this table, the stability of the products containing 0.002% or more of tocopherol was significantly improved. Table 1 Example 2 1%, 2%, and 3% of Hakama corn oil (tocopherol content 0.09240%) was added to the clear macadamia nut oil (tocopherol-free) obtained in Example 1. , 10
% of each were prepared, and the AOM stability was measured together with macadamia nut oil and refined corn.The results are shown in Table 2 along with the tocopherol content.

この表から明らかなようにコーン油を2〜10%配合し
、トコフェロール含有量を0.002%以上にしたもの
は安定性が顕著に向上していた。第2表 実施例 3 実施例1で得られた清澄なマカダミアナツツ油(酸化防
止剤無添加のもの)にオリーブ油(トコフェロール含有
量0.01100%)を10%、20%、30%、40
%、50%、60%、70%、80%、90%配合した
ものをそれぞれ調製し、マカダミアナッッ油、オリーブ
油とともにAOM安定度を測定した結果をトコフェロー
ル含有量、ヘキサデセン酸含有量とともに第3表に示し
た。
As is clear from this table, stability was significantly improved in products containing 2 to 10% corn oil and having a tocopherol content of 0.002% or more. Table 2 Example 3 Olive oil (tocopherol content 0.01100%) was added to the clear macadamia nut oil (without antioxidants) obtained in Example 1 at 10%, 20%, 30%, 40%.
%, 50%, 60%, 70%, 80%, and 90% were prepared, and the AOM stability was measured along with macadamia nut oil and olive oil. The results are shown in Table 3 along with the tocopherol content and hexadecenoic acid content. It was shown to.

この表から明らかなようにトコフェロール含有量を0.
002%以上にすることによって安定性は向上するが、
マカダミアナッッ油の含有量が30%以下またはへキサ
デセン酸含有量が7%では十分な安定性が得られなかっ
た。第3表 実施例 4 実施例1で得られた清澄なマカダミアナッッ油を(酸化
防止剤無添加のもの)を真空下で105℃に加熱、活性
白土1%を添加、5分間脱色処理し、得られた脱色油を
真空下で190℃に加熱、水蒸気を2時間吹き込み、脱
臭処理し、得られた精製マカダミアナッツ油に市販トコ
フェロール(純度98%)を0.02%添加し、高安定
性油を得た。
As is clear from this table, the tocopherol content was 0.
Stability is improved by making it 0.002% or more, but
Sufficient stability was not obtained when the macadamia nut oil content was 30% or less or the hexadecenoic acid content was 7%. Table 3 Example 4 The clear macadamia nut oil obtained in Example 1 (no antioxidant added) was heated to 105°C under vacuum, 1% of activated clay was added, and decolorized for 5 minutes. The obtained decolorized oil was heated to 190°C under vacuum and steam was blown into it for 2 hours to deodorize it, and 0.02% of commercially available tocopherol (purity 98%) was added to the obtained refined macadamia nut oil, resulting in high stability. I got oil.

この高安定性油のAOM安定度、色調(ロピボンド比色
計、51/4インチセル使用)、耐寒性、臭い、味を市
販の椿油と比較した結果を第4表に示した。この表から
明らかなように本発明の高安定性油は、従来、最も優れ
た高安定性油として広く知られている椿油よりも安定性
、色調、臭い、味の面ではるかに優れていた。第4表 実施例 5 実施例4で得られた精製マカダミァナッッ油(トコフェ
ロールを0.02%添加したもの)30%とMCT(中
鎖脂肪酸トリグリセリド)70%を混合し、AOM安定
度を測定した結果は32独特間であり極めて高い安定性
を示していた。
Table 4 shows the results of comparing the AOM stability, color tone (using a Ropibond colorimeter, 51/4 inch cell), cold resistance, odor, and taste of this highly stable oil with commercially available camellia oil. As is clear from this table, the highly stable oil of the present invention was far superior to camellia oil, which is conventionally known as the best highly stable oil, in terms of stability, color, odor, and taste. . Table 4 Example 5 Results of measuring AOM stability by mixing 30% of the refined macadamia nut oil (added with 0.02% tocopherol) obtained in Example 4 and 70% of MCT (medium chain fatty acid triglyceride) was 32 unique, indicating extremely high stability.

この混合油は、MCTの短所である加水分解性および油
性が改善された、皮ふ感触の良い液体油である。
This mixed oil has improved hydrolyzability and oiliness, which are disadvantages of MCT, and is a liquid oil that feels good on the skin.

次に本発明の植物性高安定性油を化粧品に用いた例を示
す。
Next, an example will be shown in which the highly stable vegetable oil of the present invention is used in cosmetics.

応用例 1 クリーム (重量%) 油性成分 セタノール 5.0ステア
リン酸 2.0ピースワックス
1.0 ワセリン 5.0スクワラン
20.0実施例4で得た植物性高
安定性油・〇‐〇 乳 化 剤 親油性モノステアリン酸グリセリン
2.0
ポリオキシュチレンソルピタンモノラゥリン酸ヱステル
(2肥○) 2.0 香 料 0.5防腐剤
,酸化防止剤 適量アルカリ剤,苛性
カリ 0.05水相プロピレングリコ
ール 5精製水 47.0 精製水にプロピレングリコールを加え、70qoに加熱
して70qoに保った。
Application example 1 Cream (wt%) Oily ingredients Setanol 5.0 Stearic acid 2.0 Piece wax
1.0 Vaseline 5.0 Squalane
20.0 Highly stable vegetable oil obtained in Example 4 Emulsifying agent Lipophilic glyceryl monostearate
2.0
Polyoxybutylene Sorpitan Monolaurate (2 fertilizers) 2.0 Fragrance 0.5 Preservatives, antioxidants Appropriate amount Alkaline agent, caustic potash 0.05 Aqueous phase propylene glycol 5 Purified water 47.0 In purified water Propylene glycol was added and heated to 70 qo and maintained at 70 qo.

水相以外の他の成分を混合し加熱溶解して70qoに加
熱し、この油相部を前述の水相部に加えて予備乳化後、
ホモミキサ−で均一乳化し、熱交換器により30qoま
で冷却して上記配合のクリームを得た。このクリ−ムは
皮膚によくなじみ、長期間保存してもにおし、および使
用感の経時変化はなく良好であった。
Components other than the aqueous phase are mixed and dissolved by heating to 70 qo, and this oil phase is added to the aqueous phase and pre-emulsified, then
The mixture was uniformly emulsified using a homomixer and cooled to 30 qo using a heat exchanger to obtain a cream having the above formulation. This cream blended well with the skin, and even after long-term storage, there was no odor or change in the feeling of use over time, and the cream was good.

応用例 2 乳液 (重量%) 油性成分 流動パラフィン 5.0実施
例5で得た植物性高安定性油5.0ワセリン
3.0セタノール
2.0乳化剤 ソルビタンセスキオレィン酸ェ
ステル
0.8ポリオキシェチレンオレイルエーナル(2庇0)
1.2 香 料 03防腐剤,
酸化防止剤 適量保 温 剤 ポリエ
チレングリコール600 5.0アルコール エタノー
ル 5.0精 製 水
52.5粘 度 質 カルポキシビ
ニルポリマー(1.0%水溶液)
20.0アルカリ剤 トリエタノールアミン
0.1精製水にポリエチレングリコーン600
を加えて加熱混合し、エタノールを加えて7000に保
った。
Application example 2 Emulsion (wt%) Oil component Liquid paraffin 5.0 Highly stable vegetable oil obtained in Example 5 5.0 Vaseline
3.0 cetanol
2.0 Emulsifier Sorbitan sesquioleate
0.8 polyoxyethylene oleyl enal (2 eaves 0)
1.2 Flavor 03 Preservatives,
Antioxidant Appropriate amount Insulating agent Polyethylene glycol 600 5.0 Alcohol Ethanol 5.0 Purified water
52.5 Viscosity Quality Carpoxyvinyl polymer (1.0% aqueous solution)
20.0 Alkaline agent Triethanolamine 0.1 Polyethylene glycone 600 in purified water
was added, heated and mixed, and ethanol was added to maintain the temperature at 7,000.

予め調製してあったカルボキシビニルポリマー水溶液と
アルカリ剤とを除く他の親油性成分を混合加熱して70
こ0とした。この油相部を前述の水相部に加えて予備乳
化後、カルボキシビニルポリマー水溶液を加えて均一に
混和し、アルカリ剤を加えて中和後ホモミキサーで均一
に乳化し、熱交換器により30qoまで冷却して上記配
合の乳液を得た。この乳液の皮膚への親和曲ま極めて良
好で、ベタつきがなく、且つ長期間の保存によってにお
し、および使用感の経時変化はなく良好であった。応用
例 3口紅 (重量%) 二酸化チタン 5.0赤色
204号 0.6だし
、だし、203号 1.0
キヤンデリラロウ 9.0
固形パラフィン 8.0力ルナ
ウバロウ 5.0ラノリ
ン 11‐0ヒマシ油
30.0実施例4で得た植物
性高安定性油 19.8ミリスチン酸ィソプロピ
ル 10.0香 料
適量酸化防止剤
適量二酸化チタン、赤色204号、だし、だい203
号をヒマシ油の一部に加えローラーで処理した(顔料部
)。
A pre-prepared carboxyvinyl polymer aqueous solution and other lipophilic components except the alkaline agent were mixed and heated to 70%
It was set to 0. This oil phase was added to the above-mentioned aqueous phase and pre-emulsified, then a carboxyvinyl polymer aqueous solution was added and mixed uniformly, an alkali agent was added and neutralized, then uniformly emulsified with a homomixer, and 30 qo was added with a heat exchanger. The emulsion was cooled to a temperature of 100.degree. C. to obtain a milky lotion having the above composition. This emulsion had very good affinity to the skin, was not sticky, and had no odor or change in feel over time after long-term storage. Application example 3 Lipstick (wt%) Titanium dioxide 5.0 Red No. 204 0.6 Dashi, Dashi, No. 203 1.0
Kyan Deli La Row 9.0
Solid paraffin 8.0 strength Lunauba wax 5.0 lanolin 11-0 castor oil
30.0 Highly stable vegetable oil obtained in Example 4 19.8 Isopropyl myristate 10.0 Flavor
Appropriate amount of antioxidant
Appropriate amount of titanium dioxide, red No. 204, dashi, Dai 203
The pigment was added to a portion of castor oil and processed with a roller (pigment part).

別に赤色223号を徴量ヒマシ油およびマカダミア油の
一部に溶解した(染料部)。他の成分を混合し加熱融解
した後、顔料部、染料部を加え、ホモミキサ−で均一に
分散後、型に流し込み急冷し、スチック状になったもの
を容器に差し込みフレーミングをおこない口紅を得た。
この口紅は感触、つやが非常に良好で、経時変化も非常
に少なかった。
Separately, Red No. 223 was dissolved in a portion of castor oil and macadamia oil (dye part). After mixing the other ingredients and heating and melting, add the pigment part and dye part, disperse uniformly with a homomixer, pour into a mold, rapidly cool, insert the stick-like material into a container and perform framing to obtain a lipstick. .
This lipstick had a very good feel and gloss, and showed very little change over time.

応用例 4 サンタル化粧料 (重量%) 紫外線吸収剤 1.5流動パ
ラフィン61.0実施例5で得た植物性高安定性油
37.0香 料 適
量酸化防止剤 適量上記の
配合組成のサンタン化粧料は、皮膚に塗布しやすく、経
時変化も非常に少なかった。
Application example 4 Santal cosmetics (wt%) Ultraviolet absorber 1.5 Liquid paraffin 61.0 Highly stable vegetable oil obtained in Example 5
37.0 Fragrance: Appropriate amount Antioxidant: Appropriate amount The suntan cosmetic with the above composition was easy to apply to the skin and showed very little change over time.

応用例 5ヘアオイル (重量%) 流動パラフィン 80.0オリ
ーヴ油 9.0実施例1
で得たマカダミアナッッ油(酸化防止剤無添加)
10.0酸化防止剤
適量香 料
適量上記の配合組成のヘアオイルは、長期間安
定であり使用感も良好であった。
Application example 5 Hair oil (wt%) Liquid paraffin 80.0 Olive oil 9.0 Example 1
macadamia nut oil (no antioxidant added)
10.0 Antioxidant
Appropriate amount of fragrance
Appropriate amount The hair oil with the above formulation was stable for a long period of time and had a good feel when used.

マカダミアナッッ油に酸化防止剤を直接添加しなくても
、組成分全体に添加してあれば有効である。応用例 6 ポマード (重量%) 固形パラフィン 6.0ワセ
リン 52.0
実施例1で得たマカダミアナツツ油(酸化防止剤無添加
) 30.0流動パラフ
ィン 9.0香 料
2.5酸化防止剤
適量染 料
適量上記の配合組成のポマードは、長期間安
定であり使用感も良好であった。
Even if antioxidants are not added directly to macadamia nut oil, it is effective as long as they are added to the entire composition. Application example 6 Pomade (wt%) Solid paraffin 6.0 Vaseline 52.0
Macadamia nut oil obtained in Example 1 (no antioxidant added) 30.0 Liquid paraffin 9.0 Fragrance
2.5 Antioxidants
Appropriate amount of dye
Appropriate amount The pomade with the above formulation was stable for a long period of time and had a good feel when used.

Claims (1)

【特許請求の範囲】[Claims] 1 構成脂肪酸の7〜45重量%がヘキサデセン酸とな
るようにマカダミアナツツ油を含有する液体油にトコフ
エロールを0.002〜0.2重量%含有させてなるA
OM安定度100時間以上の物性高安定性油。
1 A made by adding 0.002 to 0.2 weight % of tocopherols to a liquid oil containing macadamia nut oil so that 7 to 45 weight % of the constituent fatty acids are hexadecenoic acid.
Highly stable oil with OM stability of over 100 hours.
JP6257381A 1981-04-27 1981-04-27 vegetable high stability oil Expired JPS608277B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP6257381A JPS608277B2 (en) 1981-04-27 1981-04-27 vegetable high stability oil

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP6257381A JPS608277B2 (en) 1981-04-27 1981-04-27 vegetable high stability oil

Publications (2)

Publication Number Publication Date
JPS57179297A JPS57179297A (en) 1982-11-04
JPS608277B2 true JPS608277B2 (en) 1985-03-01

Family

ID=13204171

Family Applications (1)

Application Number Title Priority Date Filing Date
JP6257381A Expired JPS608277B2 (en) 1981-04-27 1981-04-27 vegetable high stability oil

Country Status (1)

Country Link
JP (1) JPS608277B2 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0389585U (en) * 1989-12-27 1991-09-12

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0459894A (en) * 1990-06-29 1992-02-26 Nippon Oil Co Ltd Lubrication oil composition
US7691397B2 (en) 2001-07-27 2010-04-06 International Flora Technologies, Ltd. Ultra-stable composition comprising Moringa oil and its derivatives and uses thereof

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0389585U (en) * 1989-12-27 1991-09-12

Also Published As

Publication number Publication date
JPS57179297A (en) 1982-11-04

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