JPH01203312A - External agent for skin and hair - Google Patents

External agent for skin and hair

Info

Publication number
JPH01203312A
JPH01203312A JP2508988A JP2508988A JPH01203312A JP H01203312 A JPH01203312 A JP H01203312A JP 2508988 A JP2508988 A JP 2508988A JP 2508988 A JP2508988 A JP 2508988A JP H01203312 A JPH01203312 A JP H01203312A
Authority
JP
Japan
Prior art keywords
lanolin
acetic acid
hair
skin
liquid
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.)
Pending
Application number
JP2508988A
Other languages
Japanese (ja)
Inventor
Takeshi Koresawa
是沢 猛
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.)
KUROODA JAPAN KK
Original Assignee
KUROODA JAPAN 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 KUROODA JAPAN KK filed Critical KUROODA JAPAN KK
Priority to JP2508988A priority Critical patent/JPH01203312A/en
Publication of JPH01203312A publication Critical patent/JPH01203312A/en
Pending legal-status Critical Current

Links

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
    • A61K8/92Oils, fats or waxes; Derivatives thereof, e.g. hydrogenation products thereof
    • A61K8/925Oils, fats or waxes; Derivatives thereof, e.g. hydrogenation products thereof of animal origin
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q1/00Make-up preparations; Body powders; Preparations for removing make-up
    • A61Q1/02Preparations containing skin colorants, e.g. pigments
    • A61Q1/04Preparations containing skin colorants, e.g. pigments for lips
    • A61Q1/06Lipsticks
    • 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
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q5/00Preparations for care of the hair

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)
  • Zoology (AREA)
  • Chemical & Material Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Birds (AREA)
  • Epidemiology (AREA)
  • Dermatology (AREA)
  • Cosmetics (AREA)

Abstract

PURPOSE:To obtain the present external agent containing highly purified acetic acid liquid lanolin and/or acetic acid lanolin, reduced in color and odor and having excellent safeness. CONSTITUTION:Liquid lanolin or lanolin is acetylated using 0.1-0.3pt.wt. acetic anhydride based on 1pt.wt. lanolin and then the acetylated lanolin is treated with an absorbent such as silica gel, active alumina, active clay or magnesium silicate to afford a purified product having <=1% polar ingredient content, which is then blended with a cosmetic such as cream, emulsion or lip color or hair cosmetic such as hair cream.

Description

【発明の詳細な説明】 (産業上の利用分野) 本発明は高度に精製された酢酸液状ラノリン及び(また
は)酢酸ラノリンを含有する色、臭いが少なく、又安全
性のすぐれた皮膚及び(または)毛髪外用剤を提供する
ものである。
Detailed Description of the Invention (Industrial Application Field) The present invention provides a highly purified acetic acid liquid lanolin and/or acetic acid lanolin containing acetic acid lanolin, which has less color, less odor, and is highly safe for the skin and/or ) provides a hair external preparation.

(従来技術) 古くよりラノリンは皮膚に対する親和性、付着性、湿潤
性がすぐれており、又抱水力がある為、クリーム、乳清
、口紅等の化粧料に配合されている。又近年、皮膚に対
する浸透性、拡散性を改良する為に、ラノリンを溶剤分
別法等により融点の高いロウ状エステル部分を取り除い
た液状ラノリンが開発され、化粧料に多用されている。
(Prior Art) Since ancient times, lanolin has been incorporated into cosmetics such as creams, whey, and lipsticks because it has excellent affinity, adhesion, and wettability to the skin, and also has water-holding power. In recent years, liquid lanolin, which is obtained by removing the waxy ester portion with a high melting point from lanolin by solvent fractionation, has been developed in order to improve skin permeability and diffusivity, and is widely used in cosmetics.

しかしながらラノリンは、場合によってアレルギー反応
を呈する事が報告されており、その主因はラノリン中の
極性成分(遊離のラノリンアルコール、ラノリン脂肪酸
及びその他の極性物質)であると言われている。液状ラ
ノリンはその製法上ラノリンよりも多くの極性成分を含
み、アレルギーの問題は、ラノリンと同様に含んでいる
。又独特の獣臭があり、化粧料に配合する場合、配合量
に注意する必要がある。
However, lanolin has been reported to cause allergic reactions in some cases, and the main cause is said to be the polar components in lanolin (free lanolin alcohol, lanolin fatty acids, and other polar substances). Liquid lanolin contains more polar components than lanolin due to its manufacturing process and has the same allergy issues as lanolin. It also has a unique animal odor, so care must be taken when adding it to cosmetics.

アレルギーの主因は、水酸基を持つ遊離のアルコール及
びその他の極性成分である為、無水酢酸を用いてアセチ
ル化する事により低アレルギー性にした酢酸ラノリンが
使用されている。又、ラノリンは鉱油に溶解してベビー
オイル等に使用されているが、その親水性のため経時的
にくもりを生じたり、沈澱したりする欠点があった。こ
のような水酸基が原因と考えられる性質をアセチル化す
る事により改良したのが酢酸ラノリンである。又、同様
の目的で最近酢酸液状ラノリンが使用されつつある。
Since the main cause of allergies is free alcohol and other polar components with hydroxyl groups, acetic acid lanolin, which is made hypoallergenic by acetylation using acetic anhydride, is used. Furthermore, lanolin is dissolved in mineral oil and used in baby oil and the like, but due to its hydrophilic nature, it has the disadvantage of becoming cloudy or precipitating over time. Lanolin acetate has been improved by acetylating properties thought to be caused by such hydroxyl groups. Also, acetic acid liquid lanolin has recently been used for the same purpose.

しかしながら、ラノリン中の極性成分は、水酸基を持つ
アルコール成分だけでなく遊離の脂肪酸、その他、組成
が不明な極性成分を含んでいる為、 1%以下にする事
は、通常のアセチル化反応では不可能であり、すでに市
販されている酢酸う゛ノリン、酢酸液状ラノリン中には
、通常2〜5%の極性成分が含まれている。又、ラノリ
ン特有の獣臭は減少しているもののやはり強く、化粧料
への配合には注意が必要である。
However, since the polar components in lanolin include not only alcohol components with hydroxyl groups, but also free fatty acids and other polar components whose composition is unknown, it is difficult to reduce the polar components to less than 1% in a normal acetylation reaction. Possible and already commercially available acetic acid vinolin and acetic acid liquid lanolin usually contain 2 to 5% of polar components. Furthermore, although the characteristic animal odor of lanolin has decreased, it is still strong, and care must be taken when incorporating it into cosmetics.

(解決手段) 本発明は、酢酸ラノリン及び酢酸液状ラノリンの上記の
様な欠点を改良する為鋭意検討した結果、ラノリン又は
、液状ラノリンをアセチル化した後、シリカゲル、活性
アルミナ、活性白土、ケイ酸マグネシウム等の吸着剤に
て処理する事により、極めて微量にまで極性成分が吸着
除去出来又、はとんど無臭にまで獣臭を取り除ける事を
発見し、本発明を完成し た。
(Solution Means) As a result of intensive studies to improve the above-mentioned drawbacks of acetic acid lanolin and acetic acid liquid lanolin, the present invention has been developed by acetylating lanolin or liquid lanolin, and then using silica gel, activated alumina, activated clay, and silicic acid. We have completed the present invention by discovering that by treating with an adsorbent such as magnesium, it is possible to adsorb and remove extremely small amounts of polar components, and to remove animal odor to the point where it is almost odorless.

アセチル化の方法は、ラノリン又は液状ラノリンに、無
水酢酸を反応させる事により容易に行なう事が出来る。
Acetylation can be easily carried out by reacting lanolin or liquid lanolin with acetic anhydride.

無水酢酸とラノリン又は、液状ラノリンとの量比は、ラ
ノリン又は液状ラノリン1部に対して、無水酢酸0.1
〜0.3部で良く、 100〜130℃にて1〜3時間
反応する事により得られる。反応後、中性になるまで温
水で洗浄する。
The ratio of acetic anhydride to lanolin or liquid lanolin is 0.1 part of acetic anhydride to 1 part of lanolin or liquid lanolin.
~0.3 part is sufficient and can be obtained by reacting at 100 to 130°C for 1 to 3 hours. After the reaction, wash with warm water until neutral.

水洗後、シリカゲル、活性アルミナ、活性白土、ケイ酸
マグネシウム等の吸着剤を添加し、吸着処理を行ない、
極性成分を取り除く、又アセチル化物をn−ヘキサン等
の非極性有機溶媒に溶解した後、吸着剤を充填したカラ
ムに通液する事により(容易に極性成分を取り除く事が
出来る。このような精製処理を行なった酢酸ラノリン及
び酢酸液状ラノリンは、クリーム、乳液、口紅等に使用
出来、今までにない使用感のすぐれた色、臭いの少ない
化粧料を得る事が出来る。又、ヘアークリームの様な頭
髪化粧品に使用した場合、光沢がすぐれ、 くし通りの
良い、さらにしっとりとした感触を毛髪に与えるすぐれ
た頭髪化粧料を得る事が出来る。クリーム類への配合量
は、特に限定するものではないが、−船釣には、0.1
〜30%(重量%)配合する事が出来る。
After washing with water, adsorbents such as silica gel, activated alumina, activated clay, and magnesium silicate are added to perform adsorption treatment.
Polar components can be easily removed (polar components can be easily removed by dissolving the acetylated product in a non-polar organic solvent such as n-hexane, and then passing the solution through a column packed with an adsorbent. The treated acetic acid lanolin and acetic acid liquid lanolin can be used in creams, emulsions, lipsticks, etc., and it is possible to obtain cosmetics with an unprecedented feeling of use, color, and little odor.In addition, it can be used in creams, emulsions, lipsticks, etc. When used in hair cosmetics, it is possible to obtain an excellent hair cosmetic that has excellent gloss, is easy to comb, and gives a moist feel to the hair.There are no particular restrictions on the amount of the compound in creams. No, but - 0.1 for boat fishing.
~30% (weight%) can be blended.

製造例−1 表−1の通り、ラノリン又は液状ラノリンに無水酢酸を
加え110℃にて1時間アセチル化した後、温水にて中
性になるまで洗浄する。
Production Example 1 As shown in Table 1, acetic anhydride is added to lanolin or liquid lanolin, acetylated at 110°C for 1 hour, and then washed with warm water until it becomes neutral.

得られたアセチル化物は、表−2の通り、2.8〜5.
5%の極性成分を含んでいる。テストNo、1にて得ら
れた酢酸ラノリン1部に、n−ヘキサン3部を加え溶解
する。このn−ヘキサン溶液を活性アルミナ3部を充填
したカラムに通した後、ざらにn−ヘキサン3部を通液
し、得られた溶出液をフラスコにとり、n−ヘキサンを
留去するとき、淡黄色のペーストが得られた、収率は、
65.8%であった。同様にテストNo、2〜4を処理
して得られたアセチル化物の収率及び極性成分の含有率
は、表−3の通りである。
As shown in Table 2, the obtained acetylated products range from 2.8 to 5.
Contains 5% polar components. Add and dissolve 3 parts of n-hexane to 1 part of acetic acid lanolin obtained in Test No. 1. After this n-hexane solution was passed through a column packed with 3 parts of activated alumina, 3 parts of n-hexane was passed through it, and the resulting eluate was taken into a flask. A yellow paste was obtained, the yield was
It was 65.8%. The yield of acetylated products and the content of polar components obtained by similarly processing Test Nos. 2 to 4 are shown in Table 3.

表−1 表−2 表−3 表−2、表−3の結果の通り、吸am!L2する事によ
り、極性成分が1%以下に低下してしる。
Table-1 Table-2 Table-3 As shown in Table-2 and Table-3, suck am! By applying L2, the polar component decreases to 1% or less.

表−2及び表−3の極性成分は、イヤトロスキャンで求
めた。
The polar components in Tables 2 and 3 were determined by IATROScan.

図−1及び図−2に極性成分の位置を示すスポット(b
)が極性成分であり、スポット(a)が酢酸ラノリン及
び酢酸液状ラノリンの主成分である。
Figures 1 and 2 show spots (b) showing the positions of polar components.
) is the polar component, and spot (a) is the main component of acetic acid lanolin and acetic acid liquid lanolin.

実施例−1 次に得られたテストNO91〜4の精製したアセチル化
物を用いて表−4の処方にてクリームを配合し、20人
のパネラ−にて、その使用感及び臭いについて評価した
Example 1 Next, a cream was formulated using the purified acetylated products of Test Nos. 91 to 4 according to the formulation shown in Table 4, and 20 panelists evaluated the feel and smell of the cream.

比較として、市販の酢酸ラノリン及酢酸液状ラノリンに
ついても同様にクリームを配合し、1す匝した。結果は
、表−5の通りである。
For comparison, commercially available lanolin acetate and liquid lanolin acetate were similarly formulated into creams and 1 scoop was added. The results are shown in Table-5.

表−4 表−′5 表−6の結果から明らかなように、使用したアセチル化
物中の極性成分が1%以下の精製酢酸ラノリン及び精製
酢酸液状ラノリンを配合した処方No−L  2は、ペ
タツキ感がなく、獣臭が少なくなっている。
Table-4 Table-'5 As is clear from the results in Table-6, formulation No. L 2 containing purified acetic acid lanolin and purified acetic acid liquid lanolin in which the polar component in the acetylated product used was 1% or less had a flattening effect. There is no smell and the animal odor is less.

処方例−1エモリエントクリーム ミツロウ           6.0重量x    
    6.0重量2セタノーII         
  5.0             5.0精製酢酸
ラノリン   8.0            8.O
IPM            17.5      
     13.5スククラン         10
,0            10.0流動n@ラフイ
ン    10.0           10.0I
リーフ゛油         4.0        
     4.0親油型モノステアリン酸り゛リセリン
          4.0本0リオキシIチレシソル
ヒ゛タシモノステ?リン酸エステル(20EO)   
 4.0 防腐剤             適量精製水    
        35.5処方例−2乳液 マイクロクリスタリンワックス           
       1.0ミツ0ウ           
                2.0精製酢酸液状
ラノリS/2.0 流動Iビラフィン                 
  3050ツル七゛タンセλキi[エート     
             4.0参〇リオキシエチ[
ンソルと1タンモノオレイン酸エステル(20EO) 
   1.0 ステア’lJン酸 1ルミニウム          
         0.2防腐剤          
   適量り” 17 tリン           
               8.0精製水    
        51.8処方例−3ヘアクリーム ミツロウ                     
        !、0重tX流動ハ0ラフィ:/  
                 35.OIPM 
                         
 10.0精製酢酸液状ラノリン       5.0
ソ轟ヒ゛タンセスtオ[−)            
       2.2ネ0す第1シlチbンソルヒ゛タ
ンtノラウレー)(20EO)   2.0防腐剤  
           適量精製水         
   44.8処方−1のエモリエントクリーム及び処
方例−2の乳液はほとんど無臭で使用後ペタツキ感がな
く、しっとりした感触を皮膚に与えるすぐれたものであ
った。又処方例−3のヘアクリームは、はとんど無臭で
、くし通りが良く、毛髪に光沢をあたえる等使用性がす
ぐれていた。
Prescription example-1 Emollient cream beeswax 6.0 weight x
6.0 weight 2 Setano II
5.0 5.0 Purified acetic acid lanolin 8.0 8. O
IPM 17.5
13.5 Sukuran 10
,0 10.0Flow n@Rough-in 10.0 10.0I
Leaf oil 4.0
4.0 Lipophilic monostearic acid lycerin 4.0 0 lyophilic monostearic acid monostearic acid monoste? Phosphoric acid ester (20EO)
4.0 Preservatives Appropriate amount of purified water
35.5 Formulation example-2 Emulsion microcrystalline wax
1.0 Mitsu 0 U
2.0 Purified Acetic Acid Liquid Lanoli S/2.0 Liquid I Biraffin
3050 Crane Seven Tanse λ Key [Eight
4.0 〇Rioxiech [
Sol and 1 tan monooleate (20EO)
1.0 stearic acid 1luminium
0.2 preservative
Appropriate amount” 17t rin
8.0 Purified water
51.8 Prescription example-3 hair cream beeswax
! , 0 heavy tX fluid ha 0 rough: /
35. OIPM

10.0 Purified acetic acid liquid lanolin 5.0
Todoroki Hitensesto [-]
2.2 1st batch Solvent (20EO) 2.0 Preservative
Appropriate amount of purified water
44.8 The emollient cream of Formulation-1 and the milky lotion of Formulation Example-2 were almost odorless, did not give a sticky feeling after use, and were excellent in giving a moist feel to the skin. The hair cream of Formulation Example 3 had excellent usability, such as being almost odorless, easy to comb, and giving shine to the hair.

【図面の簡単な説明】[Brief explanation of the drawing]

図−1は、現在市販されている酢酸ラノリン及び酢酸液
状ラノリンのイヤトロスキャンクロマトグラフ、図−2
は、本発明に係わる精製酢酸ラノリン及び精製酢酸液状
ラノリンのイヤトロスキャンクロマトグラフである。 (a)酢酸ラノリン及び酢酸液状ラノリンの主成分 (I))極性成分 皿二上 酢酸ラノリン             酢酸液状ラノ
リンイアトロスキャン 測定条件 固定相  クロマロッド 5i11  (シリカゲル)
展51I溶媒 クロロホルム 匿二又 精製酢酸ラノリン            精製酢酸液
状ラノリン(テストNo、l)           
    (テストNo、3 )イアトロスキャン 測定
条件 固定相  クロマロッド SII+(シリカゲル)展開
溶媒 クロロホルム 手続補正書 昭和63年9月コニ日 1、事件の表示 昭和63年 特許願 第25089号 2、発明の名称 皮膚及び毛髪外用剤 3、補正をする者 事件との関係     特許出願人 住所 大阪市東区徳井町1丁目37番地名称 クローダ
 ジャパン株式会社 昭和63年5月31日(発送口) 5、補正の対象 6、補正の内容 A、r願書」 (1)昭和63年1月1日施行の特許法など一部改正に
従い「(特許法第38条た だし書の規定による特許出願)」を削 除する。 (2)昭和63年1月1日施行の特許法など一部改正に
従い「特許請求の範囲に記 載された発明の数」を「請求項の数」 に補正する。 (3)発明の名称を「皮膚及び毛髪外用剤」と補正する
。 B、r明細書」 (1)第1頁の2行目の日付けを削除する。 (2)発明の名称を「皮膚及び毛髪外用剤」と補正する
。 明  細  書 1、発明の名称 皮膚及び毛髪外用剤 2、特許請求の範囲 極性成分含有率が1%以下の精製酢酸液状ラノリン及び
(または)精製酢酸ラノリンを含有する事を特徴とする
皮膚及び(または)毛髪外用剤。 3、発明の詳細な説明 (産業上の利用分野) 本発明は高度に精製された酢酸液状ラノリン及び(また
は)酢酸ラノリンを含有する色、臭いが少なく、又安全
性のすぐれた皮膚及び(または)毛髪外用剤を提供する
ものである。 (従来技術)
Figure 1 shows Iatroscan chromatographs of currently commercially available lanolin acetate and liquid lanolin acetate, and Figure 2
1 is an Iatroscan chromatograph of purified acetic acid lanolin and purified acetic acid liquid lanolin according to the present invention. (a) Main component of lanolin acetate and liquid lanolin acetate (I) Polar component dish 2-plate lanolin acetate Liquid lanolin acetate Iatoroscan Measurement conditions Stationary phase Chromarod 5i11 (silica gel)
Exhibit 51I Solvent Chloroform di-produced purified acetic acid lanolin Purified acetic acid liquid lanolin (Test No, l)
(Test No. 3) IatroScan Measuring conditions Stationary phase Chromarod SII+ (silica gel) developing solvent Chloroform Procedure amendment September 1988 Coni Date 1, Incident indication 1988 Patent application No. 25089 2, Title of the invention Skin and hair external preparations 3. Relationship with the case of the person making the amendment Patent applicant address 1-37 Tokuimachi, Higashi-ku, Osaka Name Clodagh Japan Co., Ltd. May 31, 1988 (Shipping port) 5. Subject of amendment 6 , Contents of amendments A, r application” (1) In accordance with the partial amendments to the Patent Act etc. that came into effect on January 1, 1988, “(patent application pursuant to the proviso to Article 38 of the Patent Act)” is deleted. (2) In accordance with the partial amendments to the Patent Act, etc. that came into effect on January 1, 1988, the "number of inventions stated in the scope of claims" will be amended to "the number of claims." (3) The title of the invention is amended to "External preparation for skin and hair." B, r Specification” (1) Delete the date on the second line of the first page. (2) The title of the invention is amended to "External preparation for skin and hair." Description 1, Name of the invention Skin and hair external preparation 2, Claims A skin and hair product characterized by containing purified acetic acid liquid lanolin and/or purified acetic acid lanolin with a polar component content of 1% or less or) topical hair preparation. 3. Detailed Description of the Invention (Industrial Application Field) The present invention provides a highly purified acetic acid liquid lanolin and/or acetic acid lanolin containing acetic acid lanolin, which has less color, less odor, and is highly safe for the skin and/or ) provides a hair external preparation. (Conventional technology)

Claims (1)

【特許請求の範囲】[Claims] 極性成分含有率が1%以下の精製酢酸液状ラノリン及び
(または)精製酢酸ラノリンを含有する事を特徴とする
皮膚及び(または)毛髪外用剤。
A skin and/or hair external preparation characterized by containing purified acetic acid liquid lanolin and/or purified acetic acid lanolin with a polar component content of 1% or less.
JP2508988A 1988-02-05 1988-02-05 External agent for skin and hair Pending JPH01203312A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2508988A JPH01203312A (en) 1988-02-05 1988-02-05 External agent for skin and hair

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2508988A JPH01203312A (en) 1988-02-05 1988-02-05 External agent for skin and hair

Publications (1)

Publication Number Publication Date
JPH01203312A true JPH01203312A (en) 1989-08-16

Family

ID=12156193

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2508988A Pending JPH01203312A (en) 1988-02-05 1988-02-05 External agent for skin and hair

Country Status (1)

Country Link
JP (1) JPH01203312A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH04149121A (en) * 1990-10-09 1992-05-22 Japan Happy:Kk Cosmetic
JP2001010921A (en) * 1999-07-01 2001-01-16 Kanebo Ltd Composition for external use

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH04149121A (en) * 1990-10-09 1992-05-22 Japan Happy:Kk Cosmetic
JP2001010921A (en) * 1999-07-01 2001-01-16 Kanebo Ltd Composition for external use

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