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JPS6020362B2 - cosmetics - Google Patents

cosmetics

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Publication number
JPS6020362B2
JPS6020362B2 JP14921574A JP14921574A JPS6020362B2 JP S6020362 B2 JPS6020362 B2 JP S6020362B2 JP 14921574 A JP14921574 A JP 14921574A JP 14921574 A JP14921574 A JP 14921574A JP S6020362 B2 JPS6020362 B2 JP S6020362B2
Authority
JP
Japan
Prior art keywords
wax
cosmetics
acid
semi
saturated fatty
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
JP14921574A
Other languages
Japanese (ja)
Other versions
JPS5179732A (en
Inventor
昭利 鵜飼
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.)
Nisshin Oillio Group Ltd
Original Assignee
Nisshin Oil Mills Ltd
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 Nisshin Oil Mills Ltd filed Critical Nisshin Oil Mills Ltd
Priority to JP14921574A priority Critical patent/JPS6020362B2/en
Publication of JPS5179732A publication Critical patent/JPS5179732A/en
Publication of JPS6020362B2 publication Critical patent/JPS6020362B2/en
Expired legal-status Critical Current

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  • Cosmetics (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Description

【発明の詳細な説明】 本発明は新規な基剤を配合してなる化粧料に関するもの
であり、皮膚に対する感触が軽く、かつ保存安定性のす
ぐれた基礎化粧料、メークアップ化粧料、頭髪用化粧料
およびボディー用化粧料等を提供することを目的とする
[Detailed Description of the Invention] The present invention relates to cosmetics containing a novel base, and is suitable for basic cosmetics, makeup cosmetics, and hair products that are light to the touch and have excellent storage stability. Its purpose is to provide cosmetics, body cosmetics, etc.

周知の如く、基礎化粧料に限らず〆−クアップ化粧品等
の基剤としてはワックスが用いられており、その果す役
割は重大であるが、しかし従来用いられているワックス
は必ずしも満足できるものではない。
As is well known, wax is used as a base not only for basic cosmetics but also for makeup products, etc., and its role is important, but the waxes conventionally used are not always satisfactory. .

すなわち従来あるワックスに、人体の皮脂と同じ融点を
もつワックスは見あたらない。そのため低融点の油性基
剤と高融点のワックスを混合して用いなければならない
。また従来あるワックスは結晶性をもつこと、融点が人
体の体温と大きな差があるために貯蔵期間中に分離、晶
出、鯵出、発汗などの現象をおこし製品の価値を箸るし
く低下させる。その場合混和剤によりある程度製品の安
定化をはかることもできるが根本的な解決ではない。ま
た一般に用いられているワックスは非常に高級な脂肪酸
またはアルコールのェステルを主体とするために皮膚に
対する感触は非常に重く、多様化するュ−ザーの好みに
合いにくいなどの欠点を有している。ラノリンには上記
諸欠点がなく、人間の皮脂と似た性質をもっている数少
ないワックスのひとつであるが、天然物であるため供給
量および価格は不安定であるし、その複雑な組成のため
原因不明確なラノリンアレルギーを引き起こすことがあ
るという欠点を有する。
In other words, among the existing waxes, there is no wax that has the same melting point as the human body's sebum. Therefore, it is necessary to use a mixture of a low melting point oil base and a high melting point wax. In addition, conventional waxes have crystallinity and have a melting point that is significantly different from the human body temperature, which causes phenomena such as separation, crystallization, abrasion, and sweating during storage, which significantly reduces the value of the product. . In this case, it is possible to stabilize the product to some extent by using an admixture, but this is not a fundamental solution. In addition, commonly used waxes are mainly composed of very high-grade fatty acids or alcohol esters, so they have the disadvantage of being very heavy to the touch and difficult to suit the diversifying tastes of users. . Lanolin is one of the few waxes that does not have the above disadvantages and has properties similar to human sebum, but as it is a natural product, the supply and price are unstable, and its complex composition causes no problems. It has the disadvantage that it can cause a definite lanolin allergy.

本発明者等は人間の表面脂質と同じような性質・挙動を
皮膚面において有するようなワックス、すなわち人間の
体温で融解する、結晶性を有しない、そして皮膚呼吸を
妨害しないような半固体ワックスの製造法について鋭意
検討の結果、上記条件を全て満足する半固体ワックスと
して、高級直鏡状飽和脂肪酸と高級側鎖状飽和脂肪酸と
よりなる合成トリグリセリドを見出した。
The present inventors have developed a wax that has properties and behavior similar to human surface lipids on the skin surface, that is, a semisolid wax that melts at human body temperature, does not have crystallinity, and does not interfere with skin breathing. As a result of extensive research into the production method, we discovered a synthetic triglyceride consisting of a higher linear saturated fatty acid and a higher side chain saturated fatty acid as a semi-solid wax that satisfies all of the above conditions.

すなわち本発明は、上記合成トリグリセリドを配合する
ことを特徴とする化粧料に係る。高級直鎖状飽和脂肪酸
とは、一般式RCOOHで表わされる脂肪酸のアルキル
基Rが直鎖状かつ飽和であるものをいい、高級側鎖状飽
和脂肪酸とは、上記のアルキル基が側鎖状かつ飽和であ
るものをいい、またアルキル基の炭素数は高級直鏡状飽
和脂肪酸においては14〆上であること、高級側鎖状飽
和脂肪酸においては炭素数8以上であることが本発明に
おいては適当である。
That is, the present invention relates to a cosmetic composition containing the above-mentioned synthetic triglyceride. A higher linear saturated fatty acid refers to a fatty acid represented by the general formula RCOOH in which the alkyl group R is linear and saturated, and a higher side chain saturated fatty acid refers to a fatty acid in which the alkyl group R is linear and saturated. In the present invention, it is suitable that the number of carbon atoms in the alkyl group is 14 or more in higher straight mirror saturated fatty acids, and 8 or more in higher side chain saturated fatty acids. It is.

また脂肪酸は2種類以上炭素数が異なるものを混合して
用いてもよい。高級直鎖状飽和脂肪酸と高級側鎖状飽和
脂肪酸との比は両脂肪酸の炭素数により適当な配合を決
める必要があるが、高級直鎖状飽和脂肪酸および高級側
鎖状飽和脂肪酸はそれぞれ少なくとも30%以上含んで
いることが、化粧品用半固体ワックスを得るには必要で
ある。
Further, two or more types of fatty acids having different numbers of carbon atoms may be used as a mixture. The ratio of higher linear saturated fatty acids and higher side chain saturated fatty acids needs to be determined appropriately depending on the number of carbon atoms in both fatty acids. % or more is necessary to obtain a semi-solid wax for cosmetics.

本発明に係る合成トリグリセリドは高級直鎖状飽和脂肪
酸および高級側鎖状飽和脂肪酸グリセリンを公知の方法
でェステル化して得られる。
The synthetic triglyceride according to the present invention is obtained by esterifying higher linear saturated fatty acids and higher side chain saturated fatty acids glycerin by a known method.

ェステル化には、例えば酸ハラィドを利用する方法、ェ
ステル基交換法、無触媒および触媒存在下、常圧または
減圧下でのェステル化反応等が採用できる。ェステル化
反応終了後、常法に従って反応混合物をアルカリ脱酸、
脱色剤による脱色ついで水蒸気蒸留による脱臭精製を行
なったものはいずれも寒色無臭で皮膚に対して刺激を与
えず、また皮膚に対して優れた感触を有する非結晶性で
、融点30一50こ○の半固体ワックスとなり化粧料用
基剤として優れた性質を有している。
For esterification, for example, a method using an acid halide, an ester group exchange method, an esterification reaction without a catalyst or in the presence of a catalyst, under normal pressure or reduced pressure, etc. can be adopted. After the esterification reaction is completed, the reaction mixture is deoxidized with an alkali according to a conventional method.
All products that have been decolorized using a decolorizing agent and deodorized and purified using steam distillation are cool-colored, odorless, non-irritating to the skin, and non-crystalline with an excellent feel to the skin, with a melting point of 30-50. It is a semi-solid wax with excellent properties as a base for cosmetics.

本基剤で従来使われていた高融点のワックスおよび液状
油性基剤との混合物の全部または一部をおきかえること
により、高融点ワックスの持っていた結晶性による問題
を容易に解決することができる。また本発明による半固
体ェステルは人間の体温とほぼ同じ温度で熔解するとい
う性質をもっているので、半固体ェステルを配合した化
粧品は皮膚面への感触が優れており、ワセリン、ラノリ
ンなどにおきかえて使用することができる。次に本発明
に係る半間体ワックスの合成例を示す。
By replacing all or part of the mixture of high melting point wax and liquid oil base conventionally used in this base, the problems caused by the crystallinity of high melting point waxes can be easily solved. . In addition, the semi-solid ester of the present invention has the property of melting at approximately the same temperature as human body temperature, so cosmetics containing the semi-solid ester have an excellent feel on the skin and can be used in place of petrolatum, lanolin, etc. can do. Next, an example of synthesis of the semi-solid wax according to the present invention will be shown.

合成例 1 擬伴機、温度計、窒素ガス吹込管および還流器を備えた
4つ口フラスコに2エチルヘキサン酸トリグリセラィド
1.2モル、ステアリン酸トリグリセライド2.8モル
およびソジウムメチラートを全仕込量に対して0.3%
加え、9ぴ0で30分間加熱した。
Synthesis Example 1 1.2 moles of 2-ethylhexanoic acid triglyceride, 2.8 moles of stearic acid triglyceride, and sodium methylate were all charged into a four-necked flask equipped with a simulator, a thermometer, a nitrogen gas blowing tube, and a reflux device. 0.3% to the amount
Then, the mixture was heated at 90°C for 30 minutes.

反応終了後常法により水洗、乾燥したものに水蒸気を吹
込んで減圧下に脱臭を行なって半固体ワックス(1)を
得た収率斑%、酸価0.01、水酸基価0.7、融点3
5〜44つoであった。合成例 2凝拝機、温度計、窒
素ガス吹込管および水分離器を備えた4つ口フラスコに
ィソステアリン酸1.4モル、パルミチン酸1.0モル
、ステアリン酸0.6モル、グリセリン1.0モルとキ
シロールおよびパラトルェンスルホン酸を全仕込量に対
してそれぞれ5%、0.2%加え、150〜260oo
にて計算量の水分離器にたまるまで反応を行なった。
After completion of the reaction, the product was washed with water and dried using a conventional method, and deodorized under reduced pressure by blowing steam into the product to obtain semi-solid wax (1). Yield unevenness %, acid value 0.01, hydroxyl value 0.7, melting point 3
There were 5 to 44 o. Synthesis Example 2 1.4 mol of isostearic acid, 1.0 mol of palmitic acid, 0.6 mol of stearic acid, and 1.0 mol of glycerin were placed in a four-necked flask equipped with a coagulator, a thermometer, a nitrogen gas blowing tube, and a water separator. Add 0 mol, xylol and para-toluene sulfonic acid at 5% and 0.2%, respectively, based on the total amount charged, and make 150 to 260 oo
The reaction was carried out until the calculated amount of water accumulated in the water separator.

その所要時間は約6時間であった。反応終了後常法によ
り脱酸、活性白土−活性炭系の脱色剤を用いて脱色後、
水蒸気を吹込み減圧下に脱臭を行なって無色無臭の半固
体ワックス(n)を得た。収率80%、酸価0.02、
水酸基価0.8、融点38〜4か0であった。合成例
3 合成例2と同様としてミリスチン酸モノグリセリド1.
0モル、ステアリン酸0.5モル、ィソステアリン酸1
.5モルをキシロールおよび酢酸亜鉛を用いて150〜
26ぴ0で約7時間反応した。
The time required was approximately 6 hours. After the reaction is completed, deoxidize using a conventional method, and decolorize using an activated clay-activated carbon decolorizer.
Deodorization was carried out under reduced pressure by blowing in water vapor to obtain a colorless and odorless semi-solid wax (n). Yield 80%, acid value 0.02,
The hydroxyl value was 0.8 and the melting point was 38-4.0. Synthesis example
3 As in Synthesis Example 2, myristic acid monoglyceride 1.
0 mol, stearic acid 0.5 mol, isostearic acid 1
.. 150 ~ 5 mol using xylol and zinc acetate
It reacted for about 7 hours at 26 pm.

反応終了後常法にしたがって脱酸、脱色および脱臭を行
なって無色無臭の半固体ワックス(m)を得た。収率8
3%、酸価0.00水酸基価1.2、融点36〜40℃
であった。次に本発明の実施例を示す。
After the reaction was completed, deoxidation, decolorization and deodorization were carried out according to conventional methods to obtain a colorless and odorless semi-solid wax (m). Yield 8
3%, acid value 0.00, hydroxyl value 1.2, melting point 36-40℃
Met. Next, examples of the present invention will be shown.

実施例 1 口紅 1 合成例1による半固体ワックス(1).55重量部
ラノリンワツクス 10 〃マイクロク
リスタリンワツクス 10 〃グリセリントリカプリ
レート 15 〃2 レーキ
10 〃染料溶液 適量香
料 適量 上記‘1’の各成分を添加混合し、温度95〜100℃
にて加熱混合し、■の成分を添加混合したのち、口紅成
型器にて成形する。
Example 1 Lipstick 1 Semi-solid wax (1) according to Synthesis Example 1. 55 parts by weight Lanolin wax 10 Microcrystalline wax 10 Glycerin tricaprylate 15 2 Lake
10 〃Dye solution Appropriate amount Fragrance Appropriate amount Add and mix each of the ingredients in '1' above, and heat to 95-100℃.
After heating and mixing, add and mix the ingredients (1), and then mold using a lipstick molder.

実施例 2 クリーム 1 合成例2による半固体ワックス(0)25重量部 ラノリン 5〃 スクワレン 5 〃 ピースワックス 5 〃 2 ソルピタンモゾステアレート 3 〃ポリオキシ
エチレンソルビタンモノラウレート2〃イオン交換水
55 〃3 香 料
適量防腐剤 適量 上記{1ーの各成分を60〜80q0に加熱して、擬投
混合し、これに{2)の成分を加え、更に‘3}の成分
を添加混合して製造する。
Example 2 Cream 1 Semi-solid wax according to Synthesis Example 2 (0) 25 parts by weight Lanolin 5 Squalene 5 Peace wax 5 2 Solpitan mozostearate 3 Polyoxyethylene sorbitan monolaurate 2 Ion exchange water
55 〃3 Flavorings
Appropriate amount of preservative Appropriate amount It is produced by heating each of the components in {1-] above to 60 to 80q0, mixing them in a pseudo-pour mixture, adding the component in {2) thereto, and then adding and mixing the component in '3}.

Claims (1)

【特許請求の範囲】[Claims] 1 高級直鎖状飽和脂肪酸および高級側鎖状飽和脂肪酸
を、それぞれ少なくとも30%以上含有する高級脂肪酸
とグリセリンとをエステル化して得られる生成物の1種
または2種以上を配合することを特徴とする化粧料。
1. It is characterized by blending one or more products obtained by esterifying a higher fatty acid containing at least 30% or more of a higher linear saturated fatty acid and a higher side chain saturated fatty acid with glycerin. Cosmetics.
JP14921574A 1974-12-28 1974-12-28 cosmetics Expired JPS6020362B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP14921574A JPS6020362B2 (en) 1974-12-28 1974-12-28 cosmetics

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP14921574A JPS6020362B2 (en) 1974-12-28 1974-12-28 cosmetics

Publications (2)

Publication Number Publication Date
JPS5179732A JPS5179732A (en) 1976-07-12
JPS6020362B2 true JPS6020362B2 (en) 1985-05-21

Family

ID=15470350

Family Applications (1)

Application Number Title Priority Date Filing Date
JP14921574A Expired JPS6020362B2 (en) 1974-12-28 1974-12-28 cosmetics

Country Status (1)

Country Link
JP (1) JPS6020362B2 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2570771B (en) * 2017-12-08 2020-05-20 Mixergy Ltd Method of selecting a heating schedule of a hot water storage tank

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5727526Y2 (en) * 1977-08-18 1982-06-16
FR2569561B1 (en) * 1984-08-30 1990-05-18 Oreal STABLE ANTHRALIN COMPOSITION IN SATURATED FATTY ACID TRIGLYCERIDES OF PLANT ORIGIN WITH 6 TO 12 CARBON ATOMS

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2570771B (en) * 2017-12-08 2020-05-20 Mixergy Ltd Method of selecting a heating schedule of a hot water storage tank

Also Published As

Publication number Publication date
JPS5179732A (en) 1976-07-12

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