JPH075450B2 - Transparent liquid oily cosmetic - Google Patents

Transparent liquid oily cosmetic

Info

Publication number
JPH075450B2
JPH075450B2 JP22258487A JP22258487A JPH075450B2 JP H075450 B2 JPH075450 B2 JP H075450B2 JP 22258487 A JP22258487 A JP 22258487A JP 22258487 A JP22258487 A JP 22258487A JP H075450 B2 JPH075450 B2 JP H075450B2
Authority
JP
Japan
Prior art keywords
oil
skin
parts
weight
good
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 - Fee Related
Application number
JP22258487A
Other languages
Japanese (ja)
Other versions
JPS6466107A (en
Inventor
憲治 森
和壽 庄司
Original Assignee
鐘紡株式会社
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 鐘紡株式会社 filed Critical 鐘紡株式会社
Priority to JP22258487A priority Critical patent/JPH075450B2/en
Publication of JPS6466107A publication Critical patent/JPS6466107A/en
Publication of JPH075450B2 publication Critical patent/JPH075450B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/33Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
    • A61K8/37Esters of carboxylic acids
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/33Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
    • A61K8/37Esters of carboxylic acids
    • A61K8/375Esters of carboxylic acids the alcohol moiety containing more than one hydroxy group
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q19/00Preparations for care of the skin
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K2800/00Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
    • A61K2800/20Chemical, physico-chemical or functional or structural properties of the composition as a whole
    • A61K2800/26Optical properties
    • A61K2800/262Transparent; Translucent

Landscapes

  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Emergency Medicine (AREA)
  • Birds (AREA)
  • Epidemiology (AREA)
  • Dermatology (AREA)
  • Cosmetics (AREA)

Description

【発明の詳細な説明】 (産業上の利用分野) 本発明は、クエン酸トリエチルエステルを相溶化剤とし
て使用し、分枝鎖を有する液状脂肪酸エステルとエチル
アルコールとクエン酸トリエチルエステルと水とが相溶
化した、透明な液状の油性化粧料に関する。更に詳しく
は、透明良好な外観を有し、保存安定性に優れ(長期保
存しても、透明度の低下や、分離や変色,変臭を起さな
い)、塗布時(後)肌なじみに優れた皮膚にべたつき感
や油光りを与えることなく清涼感を与え、塗布後に良好
な保湿性と柔軟性としっとりとした感触と適度(良好)
のつやを付与し得る、優れた液状の油性化粧料に関す
る。
The present invention uses citric acid triethyl ester as a compatibilizer, and a liquid fatty acid ester having a branched chain, ethyl alcohol, citric acid triethyl ester and water are used in the present invention. The present invention relates to a compatibilized transparent liquid oily cosmetic composition. More specifically, it has a good transparency and excellent storage stability (does not cause deterioration of transparency, separation, discoloration, or odor even after long-term storage) and is excellent in skin familiarity (after) application. It gives a refreshing feeling without giving a sticky feeling or oily feel to the skin, and has good moisturizing properties after application, softness, and a moderate feel (good).
The present invention relates to an excellent liquid oily cosmetic capable of imparting gloss.

(従来の技術) 従来、液状の油性化粧料(化粧用油)(オイル状化粧
料)は、肌(皮膚)や毛髪に油分を保給、施与して、柔
軟性や光沢(つや)を与えかつ過度の乾燥を防止するた
めに使用(塗布)されている。
(Prior Art) Conventionally, liquid oil-based cosmetics (cosmetic oils) (oil-like cosmetics) retain and apply oil to skin (skin) and hair to impart flexibility and luster. Used (applied) to give and prevent excessive drying.

一方、液状油性化粧料における必要条件としては、
(1)塗布後の保湿性が高く、しっとりとした良好な感
触(しっとり感)を与え得ること。(2)肌なじみの良
いこと。(3)皮膚を柔らかくする(柔軟化)効果に優
れていること。(4)塗布時(後)にべたつくようなわ
るい感触(べたつき感)を与えないこと。(5)塗布後
の肌や毛髪に油光り(ギラギラしたわるい光沢)を与え
ることなく、適度良好なつやを付与し得ること。(6)
苛酷条件で長期保存しても安定で、変色や変臭(異臭の
発生)を生起することなく、外観をわるくしないこと。
(7)油溶性又は水溶性の栄養成分を安定に保持、溶存
し得ること。皮膚刺激が無く、皮膚安定性が高いこと。
等が挙げられる。
On the other hand, the necessary conditions for liquid oily cosmetics are:
(1) It has a high moisturizing property after application and can give a moist and good feeling (moist feeling). (2) Must be familiar to the skin. (3) It has an excellent effect of softening (softening) the skin. (4) Do not give a sticky feel (stickiness) when applied (after). (5) Appropriately good luster can be imparted to the skin or hair after application without giving oily light (glittery and dull gloss). (6)
It is stable even under long-term storage under severe conditions, does not cause discoloration or odor (generation of off-flavor), and does not deteriorate its appearance.
(7) Stable retention and dissolution of oil-soluble or water-soluble nutrients. No skin irritation and high skin stability.
Etc.

しかしながら、これらの諸条件を兼備し、かつ満足した
液状油性化粧料は未だ得られていない。
However, a liquid oily cosmetic satisfying these various conditions and satisfying them has not been obtained yet.

例えば、液状油(単独)からなる油性化粧料では、塗布
時(後)にべたつき感や強い油性感や油光りを肌に与
え、また液状油とエチルアルコールとからなる二層型の
油性化粧料では、前記の両成分を均一に混合するための
振盪操作に手間がかかって、不便であり、混合できても
容易に分離するので、両成分を何時も適量、塗布使用し
難い。更に、合成界面活性剤(アニオン性又は非イオン
性界面活性剤)を乳化剤(又は可溶可剤)として、油性
物質をエチルアルコールや水の中に乳化(可溶化)した
水,エチルアルコール中油型の油性化粧料は、その処方
設計及び製造条件の設定がめんみつに行なわれても、大
量生産や、工程管理が難しい等の難点がある。
For example, in the case of an oil-based cosmetic composed of a liquid oil (alone), a sticky feeling, a strong oily feeling and oiliness are given to the skin at the time of application (after), and a two-layer type oil-based cosmetic composed of a liquid oil and ethyl alcohol. However, the shaking operation for uniformly mixing both components is inconvenient, and it is inconvenient, and even if they can be mixed, they are easily separated. Therefore, it is difficult to apply a suitable amount of both components at any time. Further, synthetic surfactants (anionic or nonionic surfactants) are used as emulsifiers (or solubilizers) to emulsify (solubilize) oily substances in ethyl alcohol or water, oil in ethyl alcohol type The oil-based cosmetics described above have drawbacks such as mass production and difficult process control even if the prescription design and manufacturing conditions are carefully set.

(発明が解決しようとする問題点) 本発明者等は、上述の如き従来技術の問題点を解消する
ために鋭意、広範囲な系統的研究を行なった結果、クエ
ン酸トリエチルエステルは、界面活性能を有していない
けれども、油性物質として分枝鎖を有する液状脂肪酸エ
ステルを使用し、かつエチルアルコールと水とを使用す
るという特定の組合せ(混合)に際しては、前記両成分
間の相溶化剤として作用し、前記四成分が容易に一体的
に相溶化して透明な液状を呈しかつ保存安定性の高い油
性化粧料を生成し、しかもこの液状油性化粧料を皮膚
(毛髪)に塗布する時は、肌なじみに優れべたつき感や
油光り(前記)を与えることなく清涼感を与え、しっと
り感と共に、良好なつやと保湿性と柔軟性を付与,発現
し得ることを見出し、本発明を完成した。
(Problems to be Solved by the Invention) As a result of earnest and extensive systematic studies to solve the above-mentioned problems of the prior art, the present inventors have found that triethyl citrate has a surfactant activity. In the specific combination (mixing) of using a liquid fatty acid ester having a branched chain as an oily substance and using ethyl alcohol and water as a compatibilizer between the two components, It acts, and the four components are easily compatibilized integrally to form an oily cosmetic which exhibits a transparent liquid and has high storage stability, and when the liquid oily cosmetic is applied to the skin (hair), The present invention has been completed by finding that it is excellent in skin familiarity, gives a refreshing feeling without giving a greasy feeling or oiliness (above), and can impart and express good gloss, moisturizing property and flexibility together with a moist feeling. .

本発明の目的は、透明良好な外観を有し、保存安定性に
優れ(長期保存しても透明度の低下や、分離現象や変
色,変臭を起さない)、塗布時(後)に肌なじみに優れ
べたつき感や油光りを与えることなく清涼感を与え、し
かも塗布後に、良好な保湿性と柔軟性としっとり感と適
度良好のつやを与え得る透明液状の油性化粧料を提供す
ることにある。
The object of the present invention is to have a good transparent appearance and excellent storage stability (does not cause a decrease in transparency, separation phenomenon, discoloration, or odor even after long-term storage), skin during application (after). To provide a transparent liquid oily cosmetic which is excellent in familiarity and gives a refreshing feeling without giving a greasy feeling or oily lightness, and yet can give good moisturizing property, flexibility, moisturizing feeling and moderately good gloss after application. is there.

(問題点を解決するための手段) 即ち、本発明の透明な液状の油性化粧料は、前記目的を
達成するために、主要構成成分として、クエン酸トリエ
チルエステルと、エチルアルコールと、水と、分枝鎖を
有する液状脂肪酸エステルとを配合するという構成をと
る。
(Means for Solving Problems) That is, the transparent liquid oily cosmetic of the present invention has, in order to achieve the above-mentioned object, citric acid triethyl ester, ethyl alcohol, and water as main constituents. The composition is such that a liquid fatty acid ester having a branched chain is blended.

本発明に使用するクエン酸トリエチルエステルは、公知
化合物で、殆んど無色無臭の液体である。そして前記の
分枝鎖を有する液状脂肪酸エステルとは、分枝鎖を有
し、かつ常温下で液状の脂肪酸エステルであって、例え
ば、2−エチルヘキサン酸トリグリセライド等の分枝飽
和脂肪酸のトリグリセライド,ミリスチン酸イソプロピ
ルエステル,パルミチン酸イソプロピルエステル,ミリ
スチン酸イソセチル,ミリスチン酸オクチルドデシル,2
−エチルヘキサン酸イソセチルエステル,2−エチルヘキ
サン酸イソステアリル等の分枝飽和脂肪酸又は直鎖飽和
脂肪酸と分枝一価脂肪族アルコールとからなるエステル
が好ましく、更にその他のより好ましい分枝鎖を有する
液状脂肪酸エステルとしては、例えば、ジ−2−エチル
ヘキサン酸ネオペンチルグリコールエステル,ジ−カプ
リン酸ネオペンチルグリコールエステル,リンゴ酸ジ−
2−エチルヘキサネート,コハク酸−ジ−2−エチルヘ
キシルヘキサネート等の分枝飽和脂肪酸とグリコールか
らなるエステル、飽和ジカルボン酸と分枝飽和脂肪酸と
からなるエステル等が挙げられる。
The citric acid triethyl ester used in the present invention is a known compound and is almost colorless and odorless liquid. The liquid fatty acid ester having a branched chain is a fatty acid ester which has a branched chain and is liquid at room temperature, for example, triglyceride of a branched saturated fatty acid such as 2-ethylhexanoic acid triglyceride, Myristic acid isopropyl ester, palmitic acid isopropyl ester, isocetyl myristate, octyldodecyl myristate, 2
-Ethylhexanoic acid isocetyl ester, ester consisting of a branched saturated fatty acid such as 2-ethylhexanoic acid isostearyl or a linear saturated fatty acid and a branched monohydric aliphatic alcohol is preferable, and further more preferable branched chain Examples of the liquid fatty acid ester having include di-2-ethylhexanoic acid neopentyl glycol ester, di-capric acid neopentyl glycol ester, malic acid di-
Examples thereof include esters composed of branched saturated fatty acids such as 2-ethylhexanate and succinic acid-di-2-ethylhexylhexanate, and glycols, esters composed of saturated dicarboxylic acids and branched saturated fatty acids, and the like.

前記の分枝鎖を有する液状脂肪酸エステルは、一種又は
二種以上の組合せて使用される。その一般的な配合量
は、5〜90重量%(好ましくは10〜80重量%)で、クエ
ン酸トリエチルエステルの配合量は5〜90重量%(好ま
しくは10〜80重量%)であり、そしてクエン酸トリエチ
ルエステルと分枝鎖を有する液状脂肪酸エステルとの総
(合計)配合量は18〜92重量%(好ましくは30〜90重量
%)である。前記両成分の各配合量及び総配合量が前記
の範囲外であると、前記目的を達成することが難しい。
The liquid fatty acid ester having a branched chain is used alone or in combination of two or more. Its typical loading is 5 to 90% by weight (preferably 10 to 80% by weight), the loading of citric acid triethyl ester is 5 to 90% by weight (preferably 10 to 80% by weight), and The total (total) blending amount of the citric acid triethyl ester and the branched liquid fatty acid ester is 18 to 92% by weight (preferably 30 to 90% by weight). If the amount of each component and the total amount of both components are out of the above ranges, it is difficult to achieve the above object.

本発明に使用するエチルアルコールは通常に使用されて
いるものであればよく、例えば、未変性エタノール,各
種変性エタノール等が使用される。その配合量は50〜80
重量%、好ましくは10〜70重量%である。5重量%より
も少ないと、保存安定性,透明性,感触(清涼感)等が
低下し、80重量%よりも多くなると、保存安定性,感触
等が低下する傾向がある。
The ethyl alcohol used in the present invention may be one that is commonly used, and for example, undenatured ethanol, various denatured ethanol and the like are used. The blending amount is 50-80
%, Preferably 10-70% by weight. If it is less than 5% by weight, the storage stability, transparency, feel (cooling feeling), etc. will deteriorate, and if it exceeds 80% by weight, the storage stability, feel, etc. will tend to decrease.

本発明に使用さる水は、イオン交換水,蒸留水等の精製
水であればよく、その配合量は2〜10重量%、好ましく
は3〜7重量%である。2重量%よりも少ないと感触
(肌なじみ)や保湿性が悪く、10重量%よりも多くなる
と保存安定性や外観(透明性)が悪くなる傾向がある。
The water used in the present invention may be purified water such as ion-exchanged water and distilled water, and the compounding amount thereof is 2 to 10% by weight, preferably 3 to 7% by weight. If it is less than 2% by weight, the feel (skin familiarity) and moisture retention will be poor, and if it is more than 10% by weight, storage stability and appearance (transparency) will tend to be poor.

本発明の液状の油性化粧料には、上記成分の他にγ−オ
リザノール,ビタミンA,ビタミンE,ビタミンEニコチン
酸エステル,セラミド,グルコシルセラミド,ガラクト
シルセラミド,コレステロール等の油溶性栄養剤,プラ
センター,ヒアルロン酸,アミノ酸,ムコポリサッカラ
イド,ピタミンC,ビタミンB15,コラーゲン等の水溶性栄
養剤を安定に溶存(配合)せしめ得るのも本発明の一つ
の特長である。本発明には更に、色素,香料,防腐剤等
の慣用添加成分を配合することもできる。
In the liquid oily cosmetic of the present invention, in addition to the above-mentioned components, γ-oryzanol, vitamin A, vitamin E, vitamin E nicotinic acid ester, ceramide, glucosylceramide, galactosylceramide, cholesterol and other oil-soluble nutrients, placenta It is also one of the features of the present invention that a water-soluble nutrient such as hyaluronic acid, amino acid, mucopolysaccharide, pitamine C, vitamin B15, and collagen can be stably dissolved (blended). The present invention may further contain conventional additives such as dyes, fragrances and preservatives.

本発明の液状の油性化粧料は、フェイシャルオイル,ボ
ディーオイル,サンオイル,ベビーオイル,ヘアーオイ
ル等の化粧料に適用することができる。
The liquid oily cosmetic of the present invention can be applied to cosmetics such as facial oil, body oil, sun oil, baby oil and hair oil.

(実施例) 以下の実施例に部とは重量部を、%とは重量%を意味す
る。また、実施例に示す外観(透明性),保存安定性
(変色,変臭の有無),保湿性,実用特性(塗布後の皮
膚柔軟性,しっとり感,べたつき感の有無,油光り,適
度良好なつやの有無,皮膚刺激の有無)の試験法は下記
の通りである。
(Example) In the following examples, "part" means "part by weight" and "%" means "% by weight". In addition, the appearance (transparency), storage stability (whether there is discoloration or odor), moisturizing property, practical properties (skin softness after application, moist feeling, presence or absence of sticky feeling, oiliness, moderately good) shown in Examples The test method for the presence of luster and the presence of skin irritation) is as follows.

(1) 外観(透明性) 試料を5℃の恒温室に1日間保存した後の試料の透明性
を肉眼観察して、透明(○),やや白濁(△),白濁
(×)に区別して評価した。
(1) Appearance (transparency) After the sample was stored in a thermostatic chamber at 5 ° C for 1 day, the transparency of the sample was visually observed and distinguished into transparent (○), slightly cloudy (△), and cloudy (x). evaluated.

(2) 保存安定性 試料を45℃の恒温室に3ケ月間保存した後の、色の変化
の有無,匂いの変化(変臭)の有無,透明性の変化の有
無をしらべた。
(2) Storage stability After the sample was stored in a thermostatic chamber at 45 ° C for 3 months, the presence or absence of color change, odor change (odour), and transparency change were examined.

(3) 実用特性 パネラー20人によって、実用テストを行ない、肌なじみ
が良い,清涼感があった,皮膚が柔らかくなった,しっ
とり感を与えた,べたつき感を与えた,良好なつやを与
えた,皮膚刺激を与えた,と答えた各人数を示した。
(3) Practical characteristics Practical tests were carried out by 20 panelists, and the skin was familiar, had a refreshing feeling, had soft skin, gave a moist feeling, gave a sticky feeling, and gave good luster. The number of people who gave skin irritation was shown.

(4) 化粧(塗布)後の保湿性 I.B.S社製のインピーダンスメーター(IBS−354型)を
用いて測定した。なお測定は20℃の恒温室において、一
定量(0.2g/4cm2)の試料を成人男子の上腕部に塗布
後、経時的にコンダクタンス(単位はマイクロモー)を
測定して行なった。コンダクタンスが大きいほど、一般
に皮膚の電気抵抗が小さく、皮膚表面の保湿性が良いと
言われている。
(4) Moisture retention after makeup (application) It was measured using an impedance meter (IBS-354 type) manufactured by IBS. The measurement was carried out in a thermostatic chamber at 20 ° C. by applying a fixed amount (0.2 g / 4 cm 2 ) of the sample to the upper arm of an adult male and then measuring the conductance (unit: micromho) over time. It is generally said that the larger the conductance, the smaller the electric resistance of the skin and the better the moisturizing property of the skin surface.

実施例1(フェイシャルオイル) クエン酸トリエチルエステル(以下、CTEと略記)10部
とエチルアルコール10部と、水5部と、ジ−2−エチル
ヘキサン酸ネオペンチルグリコールエステル(以下、D2
EHPGと略記)75部を30℃で攪拌下に混合して、本発明の
フェイシャルオイルを得た。得られたフェイシャルオイ
ルは、透明な液状で、保存安定性は良く、変色,変臭,
透明度の低下は何れも全く無かった。また、肌なじみが
良いと答えた人数は20人中20人、塗布時清涼感を感じた
と答えた人数が20人中19人、塗布後に皮膚が柔やかくな
ったと答えた人数が20人中19人、しっとり感を与えたと
答えた人数が20人中18人、べたつき感があったと答えた
人数が20人中0人、油光りが無く、良好なつやを与えた
と答えた人数が20人中18人、皮膚刺激を与えたと答えた
人数が20人中0人であった。そして塗布後の保湿性は、
コンダクタンス(マイクロモー)が直後(2分後)で35
0、10分後で13、30分後で11であり、良好であった。
Example 1 (Facial Oil) 10 parts citric acid triethyl ester (hereinafter abbreviated as CTE), 10 parts ethyl alcohol, 5 parts water, and di-2-ethylhexanoic acid neopentyl glycol ester (hereinafter D2)
75 parts by abbreviated as EHPG) were mixed with stirring at 30 ° C. to obtain a facial oil of the present invention. The obtained facial oil is a transparent liquid, has good storage stability, discoloration, odor,
There was no decrease in transparency at all. In addition, 20 people out of 20 responded that they were familiar with the skin, 19 out of 20 responded that they felt a refreshing feeling during application, and 20 out of 20 answered that the skin became soft after application. 19 people, 18 people out of 20 people answered that they gave a moist feeling, 0 people out of 20 people who answered that they had a sticky feeling, and 20 people who answered that they gave good luster without oiliness. 18 out of 20 and 0 out of 20 responded that they gave skin irritation. And the moisturizing property after application is
Immediately after conductance (micro mho) (2 minutes later) 35
0, 10 minutes later, 13 and 30 minutes later 11 were good.

実施例2(フェイシャルオイル) CTE75部,エチルアルコール10部,水5部,D2EHPGを10部
使用する他は実施例1と同様に行なった。得られた本発
明のフェイシャルオイルは、透明な液状で、保存安定性
は良く、変色,変臭,透明度の低下の何れもが皆無であ
った。肌なじみが良いと答えた人数は20人中20人、塗布
時清涼感を感じたと答えた人数が20人中19人、塗布後に
皮膚が柔らかくなったが20人中19人、しっとり感を与え
たが20人中19人、べたつき感を与えたが20人中0人、油
光りが無く良好なつやを与えたが20人中18人、皮膚刺激
を与えたが20人中0人であった。そして塗布後の保湿性
は、コンダクタンス(マイクロモー)が直後で360、10
分後で14、30分後で12であり、良好であった。
Example 2 (facial oil) The same procedure as in Example 1 was carried out except that CTE of 75 parts, ethyl alcohol of 10 parts, water of 5 parts and D2EHPG of 10 parts were used. The obtained facial oil of the present invention was a transparent liquid, had good storage stability, and had no discoloration, odor change, or reduction in transparency. 20 out of 20 responded that they were familiar with the skin, 19 out of 20 responded that they felt a cool sensation when applied, and 19 out of 20 who had soft skin after application, gave a moist feeling 19 out of 20 people gave a sticky feeling, but 0 out of 20 people gave a good luster without oiliness, but 18 out of 20 people gave skin irritation but 0 out of 20 people. It was The moisturizing property after application is 360, 10 immediately after the conductance (micro mho).
It was 14 minutes later and 12 minutes after 30 minutes, which was good.

実施例3(フェイシャルオイル) CTE30部,エチルアルコール30部,水5部,D2EHPGを35部
使用する他は実施例1と同様に行なった。得られた本発
明のフェイシャルオイルは、透明な液状で、保存安定性
は良好であり、変色,変臭,透明度の低下が全く無かっ
た。肌なじみが良いと答えた人数は20人中19人、塗布時
清涼感が感じたと答えた人数が20人中19人、塗布後に皮
膚が柔らかくなったと答えた人数が20人中20人、しっと
り感を与えたと答えた人数が20人中19人、べたつき感が
あったと答えた人数が20人中0人、油光りが無く、良好
なつやを与えたと答えた人数が20人中19人、皮膚刺激を
与えたと答えた人数が20人中0人であった。保湿性は、
コンダクタンス(マイクロモー)が直後で350、10分後
で14、30分後で12であり良好であった。
Example 3 (facial oil) The same procedure as in Example 1 was carried out except that 30 parts of CTE, 30 parts of ethyl alcohol, 5 parts of water and 35 parts of D2EHPG were used. The obtained facial oil of the present invention was a transparent liquid, had good storage stability, and had no discoloration, odor, or reduction in transparency. 19 out of 20 responded that they were familiar with their skin, 19 out of 20 responded that they felt a cool sensation during application, and 20 out of 20 responded that their skin became soft after application. 19 out of 20 people answered that they gave a feeling, 0 out of 20 people who answered that they had a sticky feeling, 19 out of 20 people who answered that they gave a good luster without oiliness, 0 out of 20 people answered that they gave skin irritation. Moisturizing is
The conductance (micro mho) was 350 immediately after, 14 minutes after 10 minutes, and 12 after 30 minutes.

実施例4(フェイシャルオイル) CTE10部,エチルアルコール75部,水5部,D2EHPGを10部
使用する他は、実施例1と同様に行なった。得られた本
発明のフェイシャルオイルは、透明な液状で、保存安定
性は良好であり、変色,変臭,透明度の低下が全く無か
った。塗布後の保湿性は、コンダクタンス(マイクロモ
ー)は、直後で360、10分後で14、30分後で12であり、
良好であった。塗布後に皮膚が柔らかくなったが20人中
18人、しっとり感を与えたが20人中18人、べたつき感を
与えたが20人中0人、良好なつやを与えたが20人中18人
であった。
Example 4 (Facial Oil) The procedure of Example 1 was repeated, except that 10 parts of CTE, 75 parts of ethyl alcohol, 5 parts of water and 10 parts of D2EHPG were used. The obtained facial oil of the present invention was a transparent liquid, had good storage stability, and had no discoloration, odor, or reduction in transparency. Regarding the moisturizing property after application, the conductance (micro mho) is 360 immediately after, 14 after 30 minutes, 12 after 30 minutes,
It was good. Skin became soft after application, but out of 20
Eighteen people gave a moist feeling, but 18 out of 20 people gave a sticky feeling, but 0 out of 20 people gave a good luster, but 18 out of 20 people gave it.

比較例1(フェイシャルオイル) CTE(単独)では、塗布後に皮膚が柔やかくなったが20
人中9人でわるく、保湿性もわるく、皮膚刺激性は2人
でわるく、フェイシャルオイルとして使用し難い。
Comparative Example 1 (Facial Oil) With CTE (alone), the skin became soft after application, but 20
It is difficult for 9 people to use as facial oil, poor for moisturizing, and bad for skin irritation for 2 people.

比較例2(フェイシャルオイル) エチルアルコール50部、D2EHPG50部のフェイシャルオイ
ルでは、塗布後の皮膚の柔らかくなったが20人中10人、
皮膚刺激を与えたと答えた人数が20人中3人でわるく、
塗布後の保湿性(コンダクタンス)も悪くフェイシャル
オイルとして使用できない。
Comparative Example 2 (Facial Oil) With 50 parts of ethyl alcohol and 50 parts of D2EHPG, facial oil softened the skin after application, but 10 out of 20 people,
3 out of 20 people said that they gave skin irritation,
The moisturizing property (conductance) after application is poor and it cannot be used as a facial oil.

比較例3(フェイシャルオイル) D2EHPG(単独)では、肌なじみが良いが20人中3人、塗
布時清涼感を与えたが20人中0人、またべたつき感を与
えたが20人中12人でわるく、フェイシャルオイルとして
使用できない。
Comparative Example 3 (facial oil) D2EHPG (alone) had good skin familiarity, but 3 out of 20 gave a refreshing feeling when applied, 0 out of 20, and 12 out of 20 gave a sticky feeling. It is hard to use and cannot be used as a facial oil.

比較例4(フェイシャルオイル) エチルアルコール45部と水5部とD2EHPG50部とからなる
比較のフェイシャルオイルは、白濁しており好ましくな
い。
Comparative Example 4 (Facial Oil) A comparative facial oil consisting of 45 parts of ethyl alcohol, 5 parts of water and 50 parts of D2EHPG is cloudy and not preferable.

比較例5(フェイシャルオイル) CTE50部とエチルアルコール50部とからなる比較のフェ
イシャルオイルは、皮膚刺激を与えたと答えた人数が20
人中7人でわるく好ましくない。
Comparative Example 5 (Facial Oil) A comparative facial oil consisting of 50 parts of CTE and 50 parts of ethyl alcohol was used by 20 people who answered that it caused skin irritation.
7 out of 6 people are bad.

比較例6(フェイシャルオイル) CTE50部とD2EHPG50部とからなる比較のフェイシャルオ
イルは、保湿性がわるく、好ましくない。
Comparative Example 6 (Facial Oil) A comparative facial oil consisting of 50 parts of CTE and 50 parts of D2EHPG has poor moisture retention and is not preferable.

比較例7(フェイシャルオイル) D2EHPG(分枝鎖エステル油)の代りに流動パラフィンを
使用した他は実施例1と同様に製造した比較のフェイシ
ャルオイルは、分離していて白濁しているので外観がわ
るく、また皮膚(毛髪)に油光りして良好なつやを与え
ることができない。
Comparative Example 7 (Facial Oil) A comparative facial oil produced in the same manner as in Example 1 except that liquid paraffin was used in place of D2EHPG (branched chain ester oil) had a separated and cloudy appearance. It is not good, and the skin (hair) does not shine and cannot give good luster.

比較例8(フェイシャルオイル) D2EHPG(分枝鎖エステル油)の代りに、ヒマシ油を使用
した他は実施例1と同様に製造した比較のフェイシャル
オイルは、保存安定性がわるく、着色(変色)や変臭を
起すので実用性に乏しい。
Comparative Example 8 (Facial Oil) A comparative facial oil produced in the same manner as in Example 1 except that castor oil was used in place of D2EHPG (branched chain ester oil) had poor storage stability and was colored (discolored). It is not practical because it produces a strange odor.

比較例9(フェイシャルオイル) D2EHPG(分枝鎖エステル油)の代りに、ミンク油を使用
した他は実施例1と同様に製造した比較のフェイシャル
オイルは、やや白濁していて外観は好ましくなく、保存
安定性がわるく、変色(着色)や変臭を起しやすい。
Comparative Example 9 (Facial Oil) A comparative facial oil produced in the same manner as in Example 1 except that mink oil was used instead of D2EHPG (branched chain ester oil) was slightly cloudy and had an unfavorable appearance. Poor storage stability and easy to cause discoloration (coloring) and odor.

実施例5(ボディーオイル) L−ロイシン0.1部と水3.9部,エチルアルコール36部と
の均一混合物の中にイソプロピルミリステート30部とク
エン酸トリエチル30部を添加し均一に混合して得られた
本発明のボディーオイル、透明な外観を有する液状であ
って、保存安定性が良く、着色(変色)や変臭を起し難
く、塗布後の保湿性が良く、肌なじみが良いが20人中19
人、清涼感を与えたが20人中20人、皮膚を柔らかくした
が20人中19人、べたつき感を与えたが20人中0人、油光
りせず適度良好なつやを与えたが20人中18人で好ましい
のものであった。
Example 5 (body oil) Obtained by adding 30 parts of isopropyl myristate and 30 parts of triethyl citrate to a uniform mixture of 0.1 part of L-leucine, 3.9 parts of water and 36 parts of ethyl alcohol, and uniformly mixing. The body oil of the present invention, which is a liquid having a transparent appearance, has good storage stability, is unlikely to cause coloration (discoloration) or odor, has good moisturizing properties after application, and has good skin compatibility, but among 20 people 19
People, who gave a refreshing feeling but 20 out of 20, 19 who softened the skin 19 out of 20, who gave a sticky feeling but 0 out of 20, gave a moderately good luster without oiling Eighteen of the people were good.

実施例6(フェイシャルオイル,ヘアーオイル) CTE20部とジーカプリン酸ネオペンチルグリコールエス
テル20部とリンゴ酸ジ−2−エチルヘキサネート20部
と、コハク酸−ジ−2−エチルヘキシルヘキサネート20
部と水5部とエチルアルコール14.8部とビタミンEニコ
チン酸エステル0.1部とを混合して均一に溶解して、本
発明の透明液状の油性化粧料を得た。この油性化粧料は
フェイシャルオイル,ヘアーオイルとして適用される。
この油性化粧料は、保存安定性は良好で、変色,変臭,
透明度の低下は何れも全く無かった。塗布後には、肌な
じみが良いが20人中19人、清涼感を与えたが20人中18
人、皮膚が柔らかくなったと答えた人数が20人中19人、
べたつき感なくしっとり感を与えたと答えた人数は20人
中20人、油光りがなく良好なつやを与えたと答えた人数
は20人中19人であった。また毛髪にヘアーオイルとして
使用した結果、毛髪に良好なつやを与え、かつ毛髪を柔
らかくしたと答えた人数は20人中20人であった。また塗
布後の保湿性も実施例1と同程度に良好であった。
Example 6 (facial oil, hair oil) 20 parts CTE, 20 parts dicapric acid neopentyl glycol ester, 20 parts malic acid di-2-ethylhexanate, and 20 parts succinic acid-di-2-ethylhexylhexanate
Parts, water 5 parts, ethyl alcohol 14.8 parts and vitamin E nicotinic acid ester 0.1 parts were mixed and uniformly dissolved to obtain a transparent liquid oily cosmetic of the present invention. This oily cosmetic is applied as facial oil and hair oil.
This oily cosmetic has good storage stability, discoloration, odor,
There was no decrease in transparency at all. After application, it was good on the skin, but 19 out of 20 gave a refreshing feeling, but 18 out of 20
19 out of 20 people said that their skin became softer,
Twenty out of 20 responded that they gave a moist feeling without stickiness, and 19 out of 20 answered that they gave a good luster without oiliness. Further, as a result of using the hair as a hair oil, 20 out of 20 answered that the hair had good gloss and that the hair was softened. Further, the moisturizing property after application was as good as in Example 1.

(発明の効果) 上記の如く、本発明は、クエン酸トリエチルエステルを
相溶化剤として、前記エチルアルコールと水と分枝鎖を
有する液状脂肪酸エステルとを配合する場合は、合成界
面活性剤を使用することなく、前記四成分が一体的に相
溶化することができ、しかも透明良好な外観を有し、保
存安定性に優れ(長期保存しても透明度の低下や分離現
象や変色,変臭を起さない)、塗布時(後)、皮膚(毛
髪)にべたつき感や油光りを与えることなく、良好な保
湿性と柔軟性としっとり感と適度(良好)なつやを与え
得る優れた液状油性化粧料を工業的容易かつ有利に製造
することができ、その作用効果の特異性は著しい。
(Effects of the Invention) As described above, in the present invention, when the ethyl alcohol, water and the liquid fatty acid ester having a branched chain are blended with the triethyl citrate as a compatibilizer, a synthetic surfactant is used. The above four components can be integrally compatibilized with each other, and have a good transparent appearance and excellent storage stability (even if stored for a long period of time, deterioration of transparency, separation phenomenon, discoloration, or odor may occur. Excellent liquid oiliness that can give good moisturizing property, flexibility, moisturizing feeling and moderate (good) luster without giving sticky feeling or oily feel to the skin (hair) when applied (after) Cosmetics can be manufactured easily and advantageously industrially, and the specificity of their action and effect is remarkable.

Claims (4)

【特許請求の範囲】[Claims] 【請求項1】主要構成成分として、クエン酸トリエチル
エステルと、エチルアルコールと、分枝鎖を有する液状
脂肪酸エステルと、水とを配合してなることを特徴とす
る、透明な液状の油性化粧料。
1. A transparent liquid oily cosmetic, characterized in that citric acid triethyl ester, ethyl alcohol, a liquid fatty acid ester having a branched chain, and water are blended as main constituents. .
【請求項2】クエン酸トリエチルエステルが、5〜90重
量%(重量%は最終組成物の重量基準。以下同じ)と分
枝鎖を有する液状脂肪酸エステルが5〜90重量%の範囲
内で配合されており、そして前記両成分の総含有量が、
18〜92重量%である、特許請求の範囲第(1)項記載の
透明な液状の油性化粧料。
2. A compound containing 5 to 90% by weight of citric acid triethyl ester (% by weight based on the weight of the final composition; hereinafter the same) and 5 to 90% by weight of a liquid fatty acid ester having a branched chain. And the total content of both components is
The transparent liquid oily cosmetic according to claim (1), which is 18 to 92% by weight.
【請求項3】エチルアルコールが5〜80重量%の範囲内
で含有されている、特許請求の範囲第(1)項記載の透
明な液状の油性化粧料。
3. A transparent liquid oily cosmetic according to claim 1, which contains ethyl alcohol in an amount of 5 to 80% by weight.
【請求項4】水が2〜10重量%の範囲内で含有されてい
る、特許請求の範囲第(1)項記載の透明な液状の油性
化粧料。
4. The transparent liquid oily cosmetic according to claim 1, which contains water in an amount of 2 to 10% by weight.
JP22258487A 1987-09-04 1987-09-04 Transparent liquid oily cosmetic Expired - Fee Related JPH075450B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP22258487A JPH075450B2 (en) 1987-09-04 1987-09-04 Transparent liquid oily cosmetic

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP22258487A JPH075450B2 (en) 1987-09-04 1987-09-04 Transparent liquid oily cosmetic

Publications (2)

Publication Number Publication Date
JPS6466107A JPS6466107A (en) 1989-03-13
JPH075450B2 true JPH075450B2 (en) 1995-01-25

Family

ID=16784759

Family Applications (1)

Application Number Title Priority Date Filing Date
JP22258487A Expired - Fee Related JPH075450B2 (en) 1987-09-04 1987-09-04 Transparent liquid oily cosmetic

Country Status (1)

Country Link
JP (1) JPH075450B2 (en)

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
TW206152B (en) * 1991-03-20 1993-05-21 Kuko Seiyaku Kk
NL9201438A (en) * 1992-08-11 1994-03-01 Prospa Bv Novel pharmaceutical compositions comprising esters of omega-3 polyunsaturated acids and their use in the topical treatment of ailments.
JPH10192686A (en) * 1996-12-27 1998-07-28 Pigeon Corp Solubilizer for galactosylceramide, solubilized galactosylceramide composition, solubilization of galactosylceramide, and galactosylceramide-containing oily agent
JP4406855B2 (en) * 2000-03-17 2010-02-03 株式会社ビメーク Cosmetics
DE60120113T3 (en) * 2001-04-17 2016-04-14 The Procter & Gamble Company Refreshing compositions
US8273367B2 (en) 2001-04-17 2012-09-25 The Procter And Gamble Company Articles comprising a mint odor-free cooling agent
DE102012221460A1 (en) * 2012-11-23 2014-06-12 Beiersdorf Ag Use of triethyl citrate as a denaturant for ethanol

Also Published As

Publication number Publication date
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