JPS5936603B2 - skin cosmetics - Google Patents
skin cosmeticsInfo
- Publication number
- JPS5936603B2 JPS5936603B2 JP625576A JP625576A JPS5936603B2 JP S5936603 B2 JPS5936603 B2 JP S5936603B2 JP 625576 A JP625576 A JP 625576A JP 625576 A JP625576 A JP 625576A JP S5936603 B2 JPS5936603 B2 JP S5936603B2
- Authority
- JP
- Japan
- Prior art keywords
- oil
- content
- aromatic hydrocarbon
- indene
- hydrocarbon resin
- 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
Links
- 239000002537 cosmetic Substances 0.000 title claims description 21
- YBYIRNPNPLQARY-UHFFFAOYSA-N 1H-indene Chemical compound C1=CC=C2CC=CC2=C1 YBYIRNPNPLQARY-UHFFFAOYSA-N 0.000 claims description 32
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims description 28
- 229920006272 aromatic hydrocarbon resin Polymers 0.000 claims description 16
- 238000006116 polymerization reaction Methods 0.000 claims description 8
- 239000000203 mixture Substances 0.000 claims description 7
- 238000009835 boiling Methods 0.000 claims description 6
- 239000002994 raw material Substances 0.000 claims description 6
- 125000000217 alkyl group Chemical group 0.000 claims description 5
- 239000003054 catalyst Substances 0.000 claims description 5
- 239000003208 petroleum Substances 0.000 claims description 3
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims description 2
- 239000004480 active ingredient Substances 0.000 claims description 2
- 239000002904 solvent Substances 0.000 claims description 2
- 238000005979 thermal decomposition reaction Methods 0.000 claims description 2
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims 1
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 claims 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims 1
- 229910052794 bromium Inorganic materials 0.000 claims 1
- 239000000835 fiber Substances 0.000 claims 1
- 239000003921 oil Substances 0.000 description 41
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 26
- 229920005989 resin Polymers 0.000 description 10
- 239000011347 resin Substances 0.000 description 10
- 239000011248 coating agent Substances 0.000 description 4
- 238000000576 coating method Methods 0.000 description 4
- 239000006071 cream Substances 0.000 description 4
- 238000010586 diagram Methods 0.000 description 4
- 238000009472 formulation Methods 0.000 description 4
- 210000002374 sebum Anatomy 0.000 description 4
- 210000004243 sweat Anatomy 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- 239000004215 Carbon black (E152) Substances 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 229930195733 hydrocarbon Natural products 0.000 description 3
- 150000002430 hydrocarbons Chemical class 0.000 description 3
- 229940057995 liquid paraffin Drugs 0.000 description 3
- 230000014759 maintenance of location Effects 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 239000001993 wax Substances 0.000 description 3
- ZQXCQTAELHSNAT-UHFFFAOYSA-N 1-chloro-3-nitro-5-(trifluoromethyl)benzene Chemical compound [O-][N+](=O)C1=CC(Cl)=CC(C(F)(F)F)=C1 ZQXCQTAELHSNAT-UHFFFAOYSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- 238000004821 distillation Methods 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- 210000004709 eyebrow Anatomy 0.000 description 2
- 238000005562 fading Methods 0.000 description 2
- SZVJSHCCFOBDDC-UHFFFAOYSA-N ferrosoferric oxide Chemical compound O=[Fe]O[Fe]O[Fe]=O SZVJSHCCFOBDDC-UHFFFAOYSA-N 0.000 description 2
- 239000003205 fragrance Substances 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 239000003755 preservative agent Substances 0.000 description 2
- 238000010992 reflux Methods 0.000 description 2
- PRAKJMSDJKAYCZ-UHFFFAOYSA-N squalane Chemical compound CC(C)CCCC(C)CCCC(C)CCCCC(C)CCCC(C)CCCC(C)C PRAKJMSDJKAYCZ-UHFFFAOYSA-N 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- LDVVTQMJQSCDMK-UHFFFAOYSA-N 1,3-dihydroxypropan-2-yl formate Chemical compound OCC(CO)OC=O LDVVTQMJQSCDMK-UHFFFAOYSA-N 0.000 description 1
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 1
- 239000005995 Aluminium silicate Substances 0.000 description 1
- 239000001856 Ethyl cellulose Substances 0.000 description 1
- ZZSNKZQZMQGXPY-UHFFFAOYSA-N Ethyl cellulose Chemical compound CCOCC1OC(OC)C(OCC)C(OCC)C1OC1C(O)C(O)C(OC)C(CO)O1 ZZSNKZQZMQGXPY-UHFFFAOYSA-N 0.000 description 1
- 206010057385 Eyelid irritation Diseases 0.000 description 1
- 239000004166 Lanolin Substances 0.000 description 1
- 239000000020 Nitrocellulose Substances 0.000 description 1
- 239000004677 Nylon Substances 0.000 description 1
- KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 description 1
- 229920001800 Shellac Polymers 0.000 description 1
- 231100000460 acute oral toxicity Toxicity 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- CEGOLXSVJUTHNZ-UHFFFAOYSA-K aluminium tristearate Chemical compound [Al+3].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CEGOLXSVJUTHNZ-UHFFFAOYSA-K 0.000 description 1
- 229940063655 aluminum stearate Drugs 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 229920002301 cellulose acetate Polymers 0.000 description 1
- 230000002925 chemical effect Effects 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 210000003298 dental enamel Anatomy 0.000 description 1
- 229920001249 ethyl cellulose Polymers 0.000 description 1
- 235000019325 ethyl cellulose Nutrition 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 230000037308 hair color Effects 0.000 description 1
- 239000003676 hair preparation Substances 0.000 description 1
- 238000005342 ion exchange Methods 0.000 description 1
- WTFXARWRTYJXII-UHFFFAOYSA-N iron(2+);iron(3+);oxygen(2-) Chemical compound [O-2].[O-2].[O-2].[O-2].[Fe+2].[Fe+3].[Fe+3] WTFXARWRTYJXII-UHFFFAOYSA-N 0.000 description 1
- 230000007794 irritation Effects 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- 235000019388 lanolin Nutrition 0.000 description 1
- 229940039717 lanolin Drugs 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- -1 monopalmitate Iron trioxide Chemical compound 0.000 description 1
- JXTPJDDICSTXJX-UHFFFAOYSA-N n-Triacontane Natural products CCCCCCCCCCCCCCCCCCCCCCCCCCCCCC JXTPJDDICSTXJX-UHFFFAOYSA-N 0.000 description 1
- 229920001220 nitrocellulos Polymers 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- 229910017059 organic montmorillonite Inorganic materials 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 230000002335 preservative effect Effects 0.000 description 1
- 238000011076 safety test Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000013535 sea water Substances 0.000 description 1
- 230000028327 secretion Effects 0.000 description 1
- 239000004208 shellac Substances 0.000 description 1
- 229940113147 shellac Drugs 0.000 description 1
- 235000013874 shellac Nutrition 0.000 description 1
- ZLGIYFNHBLSMPS-ATJNOEHPSA-N shellac Chemical compound OCCCCCC(O)C(O)CCCCCCCC(O)=O.C1C23[C@H](C(O)=O)CCC2[C@](C)(CO)[C@@H]1C(C(O)=O)=C[C@@H]3O ZLGIYFNHBLSMPS-ATJNOEHPSA-N 0.000 description 1
- 235000011121 sodium hydroxide Nutrition 0.000 description 1
- 229940032094 squalane Drugs 0.000 description 1
- 238000004230 steam cracking Methods 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 239000008399 tap water Substances 0.000 description 1
- 235000020679 tap water Nutrition 0.000 description 1
- 210000001138 tear Anatomy 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 239000012085 test solution Substances 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q1/00—Make-up preparations; Body powders; Preparations for removing make-up
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/31—Hydrocarbons
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Birds (AREA)
- Epidemiology (AREA)
- Cosmetics (AREA)
Description
【発明の詳細な説明】
本発明は皮膚化粧料に関するものであり、特に従来のメ
イクアップ化粧料の欠点であった「化粧くずれ」即ち化
粧料に対する汗、涙、皮脂などの人体分泌物の作用、雨
、雪、プールの水、海水など化粧料使用時の天候、場所
の諸条件に起因する水分の作用、併用する他の化粧料中
の諸成分の作用など主に化学的作用による化粧くずれ、
これらの種々の化粧くずれを解決し、衣類も汚さない化
粧もちの良好なメイクアップ化粧料を得んとするもので
ある。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to skin cosmetics, and particularly addresses the drawbacks of conventional makeup cosmetics, such as "makeup fading", that is, the effects of human body secretions such as sweat, tears, and sebum on cosmetics. , makeup fading mainly due to chemical effects such as rain, snow, pool water, seawater, etc., moisture effects caused by the weather and location conditions when using cosmetics, and the effects of various ingredients in other cosmetics used together. ,
The purpose of the present invention is to solve these various problems of makeup smearing and to obtain a makeup cosmetic that does not stain clothes and has good makeup retention.
従来のメイクアップ化粧料には水系、油系、乳化系及び
粉末系など多種多様な製品形態のものがあるが、例えば
水系のものは処方中に親水性物質を多量に含有するため
、汗、涙、雨などにより化粧くずれし易い即ち耐水性が
不良である。Conventional makeup cosmetics come in a wide variety of product forms, including water-based, oil-based, emulsified, and powder-based products.For example, water-based products contain large amounts of hydrophilic substances in their formulations, so they can be easily absorbed by sweat, Makeup easily fades due to tears, rain, etc., ie, water resistance is poor.
油系のものは処方中に親油性物質を多量に含有するため
皮脂あるいは併用する化粧料の油分により、化粧くずれ
し易い。Since oil-based products contain a large amount of lipophilic substances in their formulations, they are likely to cause makeup to fade due to sebum or the oil content of the cosmetics used in combination.
即ち耐油性が不良である。乳化系のものは耐水性、耐油
性の何れも充分ではない。That is, oil resistance is poor. Emulsion type products do not have sufficient water resistance or oil resistance.
また、粉末系のものは耐水性、耐油性に劣り、更に使用
部位における皮膚の動き、手あるいは衣類による摩擦に
より化粧くずれし易い即ち肌への接着性が不良であるし
、衣類も汚し易い。In addition, powder-based products have poor water resistance and oil resistance, and furthermore, makeup tends to come off due to movement of the skin at the site of use or friction from hands or clothing, that is, they have poor adhesion to the skin, and they also tend to stain clothing.
このように従来のメイクアップ化粧料は耐水性、耐油性
、使用部位への接着性に劣るため化粧くずれを起し易く
、化粧もちが不良であった。As described above, conventional makeup cosmetics have poor water resistance, oil resistance, and adhesion to the area of use, and thus tend to cause makeup to come off and have poor makeup retention.
本発明は従来のメイクアップ化粧料の欠点を解決すべく
、鋭意研究の末、高軟化点芳香族系炭化水素樹脂を有効
成分として、化粧料基材に配合することにより、目的を
達成し、耐水性、耐油性及び接着性に優れた化粧くずれ
のない、化粧もちの良好なメイクアップ化粧料を得たこ
とである。In order to solve the drawbacks of conventional makeup cosmetics, the present invention has achieved the objective by blending a high softening point aromatic hydrocarbon resin as an active ingredient into a cosmetic base material after intensive research. To obtain a makeup cosmetic that has excellent water resistance, oil resistance, and adhesiveness, does not cause makeup smearing, and has good makeup retention.
本発明で使用される高軟化点芳香族系炭化水素樹脂とは
[石油類の熱分解により得られる分解油留分のうち沸点
120〜220℃、重合度1000〜19001望まし
くは沸点140〜220℃、重合度1600〜1900
の範囲内の沸点及び重合度を有し、スチレン含有量が7
wt%以下、スチレン含有率が15%以下、インデンお
よびそのアルキル誘導体の合計含有量が5wt%以上で
かつインデン含有率が11%以上に調整したものを原料
とし、フェノールまたはアルキルフェノール類の一種ま
たは二種以上の混合物を原料油に対し0.05〜5wt
%の範囲内で加えて、三ふつ化はう素糸触媒を原料油に
対して0.01〜5wt%用いて一30〜+40℃の範
囲内の温度でIQmm〜15hr の範囲内の時間で重
合した後、触媒を分解除去してさらに蒸発または蒸留に
より未反応油および低重合物を分離し、120℃以上の
高軟化点、炭什水素溶剤に対する溶解性良好、30以下
の低臭素価の淡色芳香族系炭住水素樹脂;ここでスチレ
ン含有量またはインデンおよびそのアルキル誘導体の合
計含有量は、原料となる分解油留分中のスチレンのwt
%またはインデンおよびそのアルキル誘導体の合計のw
t%を示し、スチレン含有率またはインデン含有率は下
式(1)または(2)で表される数値を示す。The high softening point aromatic hydrocarbon resin used in the present invention is [a cracked oil fraction obtained by thermal decomposition of petroleum with a boiling point of 120 to 220°C, a degree of polymerization of 1000 to 19000°C, preferably a boiling point of 140 to 220°C] , degree of polymerization 1600-1900
The boiling point and degree of polymerization are within the range of , and the styrene content is 7.
wt% or less, the styrene content is 15% or less, the total content of indene and its alkyl derivatives is 5wt% or more, and the indene content is adjusted to 11% or more. 0.05-5wt of a mixture of seeds or more based on raw oil
%, and using 0.01 to 5 wt% of trifluoride borosilicate thread catalyst to the raw material oil at a temperature of -30 to +40°C for a time of IQmm to 15 hr. After polymerization, the catalyst is decomposed and removed, and unreacted oil and low polymers are separated by evaporation or distillation. Light-colored aromatic hydrocarbon resin; Here, the styrene content or the total content of indene and its alkyl derivatives is the wt of styrene in the cracked oil fraction that is the raw material.
% or w of the sum of indene and its alkyl derivatives
t%, and the styrene content or indene content is a value expressed by the following formula (1) or (2).
但し、Aは原料分解油留分中の重合可能成分量(重量%
)、Bは原料分解油留分中のスチレンの含有量、Cは原
料分解油留分中のインデンおよびそのアルキル誘導体の
合計含有量である。However, A is the amount of polymerizable components in the raw cracked oil fraction (wt%
), B is the content of styrene in the raw cracked oil fraction, and C is the total content of indene and its alkyl derivatives in the raw cracked oil fraction.
(以下高軟什点芳香族系炭住水素樹脂と略す)と特定さ
れるものである。(hereinafter abbreviated as high soft point aromatic hydrocarbon resin).
この高軟化点芳香族系炭什水素樹脂の製造法は、特公昭
48−32432に詳しく記載されているものである。The method for producing this high softening point aromatic hydrocarbon resin is described in detail in Japanese Patent Publication No. 48-32432.
即ち、製造例の1つを示すと、ナフサのスチームクラッ
キングで副生ずる120〜220℃の範囲の分解油留分
(A)はガスクロマド分析の結果から重合可能成分は4
8.5wt%でスチレン含有量は15.0wt%であり
、インデン類含有量は3.9wt%であった。That is, to show one of the production examples, the cracked oil fraction (A) in the range of 120 to 220°C produced by steam cracking of naphtha has 4 polymerizable components according to the results of gas chromad analysis.
At 8.5 wt%, the styrene content was 15.0 wt%, and the indene content was 3.9 wt%.
従って、スチレン含有率は30.9%、インデン含有率
は8.0%となった。Therefore, the styrene content was 30.9% and the indene content was 8.0%.
(A)を30段の精留塔で張込温度150℃、塔頂温度
145℃、塔低温度175℃および還流比2.0の条件
で精留した結果、(A)の87wt%が基低から引抜か
れた。As a result of rectifying (A) in a 30-stage rectification column under the conditions of charging temperature 150 °C, tower top temperature 145 °C, tower low temperature 175 °C, and reflux ratio 2.0, 87 wt% of (A) was Pulled from low.
この油(B)の重合可能成分49.3wt%、スチレン
含有量6.2wt%、スチレン含有率12.6%、イン
デン類含有量4.5wt%、インデン含有率9.1%と
なった。This oil (B) had a polymerizable component of 49.3 wt%, a styrene content of 6.2 wt%, a styrene content of 12.6%, an indene content of 4.5 wt%, and an indene content of 9.1%.
また、(A)を上記精留塔で張込温度160℃、塔頂温
度153℃、塔低温度190℃および還流比3.5の条
件で精留した結果、分解油留分の52wt%が基低から
引き抜かれた。In addition, as a result of rectifying (A) in the above rectifying column under the conditions of charging temperature 160°C, tower top temperature 153°C, tower low temperature 190°C, and reflux ratio 3.5, 52 wt% of the cracked oil fraction was Pulled out from the base.
この油(Qの重合可能成分49.5wt%、スチレン含
有量0.1wt%、スチレン含有率0.2%、インデン
類含有量7.5wt%、インデン含有率15.2%とな
った。This oil (Q) had a polymerizable component of 49.5 wt%, a styrene content of 0.1 wt%, a styrene content of 0.2%, an indene content of 7.5 wt%, and an indene content of 15.2%.
これらの(A)、(B)および(Qの分解油および(B
)にインデン含有量55wt%の濃縮インデン留分を加
えたものを原料とし表に示した条件で重合した後、カセ
イソーダ水溶液で触媒を除去後水洗して蒸留により未反
応油および低重合物を除去して芳香族系炭化水素を得た
、結果を表に示す。The cracked oils of these (A), (B) and (Q) and (B
) to which a concentrated indene fraction with an indene content of 55 wt% was added as a raw material and polymerized under the conditions shown in the table. After removing the catalyst with an aqueous solution of caustic soda, washing with water and removing unreacted oil and low polymers by distillation. The results are shown in the table.
(注1) 原料油に対してフェノールを0.15wt%
加え、触媒として三ふつ化はう素エチルエーテル錯仕合
物を0.4wt%加えて10℃、5 hr 重合
(注2) 環球法(JIS K2531−1960)
による。(Note 1) 0.15wt% phenol based on raw oil
In addition, 0.4 wt% of trifluoride ethyl ether complex was added as a catalyst and polymerized at 10°C for 5 hours (Note 2) Ring and ball method (JIS K2531-1960)
by.
(注3) ASTMD−1158−57Tによる。(Note 3) According to ASTM D-1158-57T.
(注4) 前記石油系炭什水素溶媒に対する溶解性(注
5) 樹脂21をベンゼン25ccに溶解したものをA
STMD−1544−58Tによりガードナー標準色数
管と比色する。(Note 4) Solubility in the petroleum-based hydrocarbon solvent (Note 5) Resin 21 dissolved in 25 cc of benzene was used as A.
Compare the color with a Gardner standard color tube using STMD-1544-58T.
本発明ではこの高軟化点芳香族系炭化水素樹脂をメイク
アップ化粧料中1〜15%配合することにより目的が達
せられる。In the present invention, the object can be achieved by blending 1 to 15% of this high softening point aromatic hydrocarbon resin in makeup cosmetics.
従来の化粧料にはシェラツク、ロジンなどの天然系油溶
性樹脂、またエチルセルロース、ニトロセルロース、酢
酸セルロースなどの油溶性セルロース誘導体が用いられ
てきたが、処方中の各成分との相溶性も劣り、化粧もち
が良好であるとは言い難いものであった。Conventional cosmetics have used natural oil-soluble resins such as shellac and rosin, as well as oil-soluble cellulose derivatives such as ethyl cellulose, nitrocellulose, and cellulose acetate, but they have poor compatibility with each ingredient in the formulation. It was difficult to say that the makeup lasted well.
本発明に用いられる高軟化点芳香族炭化水素樹脂と従来
用いられていた樹脂との耐油性、耐水性及び接着性につ
いての比較データ示す。Comparative data regarding oil resistance, water resistance, and adhesion between the high softening point aromatic hydrocarbon resin used in the present invention and conventionally used resins is shown.
比較するために使われる標準処方は、酸化鉄ブラック2
5%、ワックス15%、各種樹脂10%、流動パラフイ
″ン50%とし、各種樹脂としてA〜R(樹脂記号)ま
でを使用してデータを得た。The standard formulation used for comparison is Iron Oxide Black 2
Data were obtained using A to R (resin symbols) as the various resins.
(第2図の場合)又、標準の耐油性、耐水性及び接着性
のテスト方法は次のとおりである。(In the case of Figure 2) Also, standard oil resistance, water resistance and adhesion test methods are as follows.
(1)耐油性:化粧料を塗布乾燥した板を試験紙(試験
液を一定量滴下)上に、一定回数(30回)接触させ、
試験紙上への転写の度合を比較する。(1) Oil resistance: A board coated with cosmetics and dried is brought into contact with a test paper (a certain amount of test liquid is dropped) a certain number of times (30 times).
Compare the degree of transfer onto the test paper.
(2)耐水性:試験液中に化粧料塗布膜を入れ、機械的
摩擦を加え、一定時間(2時間)振盪し、塗布膜のはが
れ具合を比較する。(2) Water resistance: A cosmetic coating film is placed in a test solution, mechanical friction is applied, shaking is performed for a certain period of time (2 hours), and the degree of peeling of the coating film is compared.
(3)接着性:ナイロン板に化粧料塗布膜をつくり、こ
れに機械的摩擦を加え、一定時間(2時間)振盪し、塗
布膜のはがれ具合を比較する。(3) Adhesion: A cosmetic coating film is made on a nylon plate, mechanical friction is applied to it, shaken for a certain period of time (2 hours), and the degree of peeling of the coating film is compared.
上記、耐油性、耐水性及び接着性の良い場合イ、悪い場
合口の状態図について第1図に示す。FIG. 1 shows the state diagram of the case where the oil resistance, water resistance and adhesion are good, and the case where it is bad.
次に、本発明に使われる高軟化点芳香族系炭化水素樹脂
と各種樹脂との耐油性、耐水性及び接着性の比較を第1
表及び第2図に示す。Next, we will compare the oil resistance, water resistance, and adhesiveness of the high softening point aromatic hydrocarbon resin used in the present invention with various resins.
It is shown in the table and Figure 2.
第1表は第2図の耐油性について定性的に表現した場合
に下記のように区別分類される。In Table 1, when qualitatively expressing the oil resistance shown in Figure 2, the oil resistance is classified as follows.
次に、本発明の実施例のクリームファンデーションと各
種ファンデーションとの耐油性、耐水性及び接着性の比
較を第3図に示す。Next, FIG. 3 shows a comparison of oil resistance, water resistance, and adhesion between the cream foundation of the example of the present invention and various foundations.
以上の如く、耐油性、耐水性及び接着性について、本発
明に使われる高軟化点芳香族系炭化水素樹脂と各種樹脂
を比較するに、耐油性は人工皮脂を、耐水性は人工汗を
用いてテストしたが第1表及び第2図に示すように各種
樹脂と比較して高軟化点芳香族系炭化水素樹脂は耐油性
が極めて良好なる結果を得た。As described above, when comparing various resins with the high softening point aromatic hydrocarbon resin used in the present invention in terms of oil resistance, water resistance, and adhesiveness, we found that artificial sebum was used for oil resistance, and artificial sweat was used for water resistance. As shown in Table 1 and Figure 2, the aromatic hydrocarbon resin with a high softening point had extremely good oil resistance compared to various resins.
又、第3図に見られるように、実施例1と各種ファンデ
ーション(油性タイプ、乳化系タイプ及び水系)との比
較を、耐油性は人工皮脂、サンクンオイル及びスクワラ
ンを、耐水性は水道水、人工汗及び人工塩水(3,5%
食塩水)を用いて行った結果、接着性を含めていずれも
良好な結果を得ることができた。Also, as seen in Figure 3, a comparison was made between Example 1 and various foundations (oil-based type, emulsified type, and water-based type). For oil resistance, artificial sebum, sunken oil, and squalane were used, and for water resistance, tap water, Artificial sweat and artificial salt water (3.5%
As a result, good results were obtained in all respects including adhesiveness.
又、高軟化点芳香族系炭化水素樹脂について皮膚−次刺
激性試験、眼瞼刺激性試験、急性経口毒性試験及び人体
閉塞パッチテストの安全性試験を行ったが、−問題はな
い結果を得た。In addition, we conducted safety tests on high softening point aromatic hydrocarbon resins including a skin secondary irritation test, an eyelid irritation test, an acute oral toxicity test, and a human body occlusion patch test, and no problems were found. .
実施例 1
クリームファンデーション
流動パラフィン(軽質) 50%炭化
水素ワックス 5ラノリン誘
導体 5高軟化点芳香族系炭
化水素樹脂 5(沸点140℃、重合度16
00)
ンルビタンモノパルミテート 3酸化鉄
(ブラウン)35
二酸什チタン 10り″り
16.5有
機モンモリロナイト 2防腐剤
適量香 料
適量実施例 2
クリームアイブロウ
流動パラフィン(軽質) 40%炭化水
素ワックス 10高軟化点芳香
族系炭化水素樹脂 15(沸点120℃、重合
度1000)
モノグリセリド 3アルミニユ
ームステアレート 1イオン交換水
15黒色酸化鉄
3カオリン
13防腐剤
適量香 料 適量
実施例1、及び2の製法
流動パラフィンに樹脂、ワックス、界面活性剤増粘剤等
を添加し、加熱溶解、分散させたものに顔料及び水(実
施例2の場合)を添加し、攪拌分散、冷却して得ること
が出来る。Example 1 Cream foundation Liquid paraffin (light) 50% hydrocarbon wax 5 Lanolin derivative 5 High softening point aromatic hydrocarbon resin 5 (boiling point 140°C, degree of polymerization 16
00) Rubitan monopalmitate Iron trioxide (brown) 35 Titanium dioxide 10
16.5 Organic montmorillonite 2 Preservative
Appropriate amount of fragrance
Appropriate amount Example 2 Cream eyebrow liquid paraffin (light) 40% hydrocarbon wax 10 High softening point aromatic hydrocarbon resin 15 (boiling point 120°C, degree of polymerization 1000) Monoglyceride 3 Aluminum stearate 1 Ion exchange water
15 black iron oxide
3 kaolin
13 Preservatives
Appropriate amount Fragrance Appropriate amount Production method of Examples 1 and 2 Add resin, wax, surfactant thickener, etc. to liquid paraffin, heat dissolve and disperse, then add pigment and water (in the case of Example 2) It can be obtained by stirring, dispersing, and cooling.
、本発明はその他のファンデーション類、アイブロウ、
アイシャドウ、アイライナー、マスカラ等のアイメイク
アップ化粧料類、ボディペイント、ネイルエナメル、口
紅、毛髪用着色料及びレッグメイクアップ化粧料等の皮
膚化粧料や頭髪化粧料に広く応用されるものである。, the present invention applies to other foundations, eyebrows,
It is widely applied to eye makeup cosmetics such as eye shadow, eyeliner, and mascara, and skin and hair cosmetics such as body paint, nail enamel, lipstick, hair coloring, and leg makeup cosmetics. be.
第1図は(1)耐油性、(2)耐水性及び(3)接着性
の良い場合イ、悪い場合口の状態図を示す。
第2図は本発明に使われる高軟化点芳香族系炭化水素樹
脂と各種樹脂(A−R)との耐油性、耐水性及び接着性
の比較図である。
第3図は本発明の実施例1のクリームファンデーション
と各種ファンデーション(油性■と■、乳化系及び水系
)との耐油性、耐水性及び接着性の比較図である。FIG. 1 shows a state diagram in which (1) oil resistance, (2) water resistance, and (3) adhesion are good and bad. FIG. 2 is a comparison diagram of the oil resistance, water resistance, and adhesiveness of the high softening point aromatic hydrocarbon resin used in the present invention and various resins (A-R). FIG. 3 is a comparison diagram of oil resistance, water resistance, and adhesion between the cream foundation of Example 1 of the present invention and various foundations (oil-based (1) and (2), emulsion-based and water-based).
Claims (1)
より得られる分解油留分のうち沸点120〜220℃、
重合度1000〜1900を有し、スチレン含有量が7
wt%以下、スチレン含有率が15%以下、インデンお
よびアルキル誘導体の合計含有量が5wt%以上でかつ
インデン含有率が11%以上に調整したものを原料とし
、フェノールまたはアルキルフェノール類の一種または
二種以上の混合物を原料油に対し0.05〜5wt%の
範囲内で加えて、三ふつ什はう素糸触媒を原料油に対し
て0.01〜5wt%用いて一30〜+40℃の範囲内
の温度で10m1n〜15 hr の範囲内の時間で重
合した後、触媒を分解除去してさらに蒸発または蒸留に
より未反応油および低重合物を分離し、120℃以上の
高軟化点、炭化水素溶剤に対する溶解性良好、30以下
の低臭素価の淡色芳香族系炭化水素樹脂である。 )を有効成分として化粧料基剤に配合することを特徴と
する皮膚化粧料。[Scope of Claims] 1. High softening point aromatic hydrocarbon resin (boiling point 120-220°C of cracked oil fraction obtained by thermal decomposition of petroleum);
It has a degree of polymerization of 1000 to 1900 and a styrene content of 7.
wt% or less, the styrene content is 15% or less, the total content of indene and alkyl derivatives is 5wt% or more, and the indene content is adjusted to 11% or more as a raw material, and one or two types of phenol or alkylphenols. The above mixture was added in the range of 0.05 to 5 wt% to the raw material oil, and the mixture was heated in the range of -30 to +40°C using 0.01 to 5 wt% of the three-piece silicate fiber catalyst to the raw material oil. After the polymerization is carried out at a temperature within It is a light-colored aromatic hydrocarbon resin with good solubility in solvents and a low bromine number of 30 or less. ) as an active ingredient in a cosmetic base.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP625576A JPS5936603B2 (en) | 1976-01-22 | 1976-01-22 | skin cosmetics |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP625576A JPS5936603B2 (en) | 1976-01-22 | 1976-01-22 | skin cosmetics |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS5290637A JPS5290637A (en) | 1977-07-30 |
JPS5936603B2 true JPS5936603B2 (en) | 1984-09-05 |
Family
ID=11633365
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP625576A Expired JPS5936603B2 (en) | 1976-01-22 | 1976-01-22 | skin cosmetics |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS5936603B2 (en) |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0759488B2 (en) * | 1984-05-31 | 1995-06-28 | ポーラ化成工業株式会社 | Makeup cosmetics |
JP2002154916A (en) * | 2000-11-22 | 2002-05-28 | Tokiwa Corp | Oily cosmetics |
US7611726B2 (en) | 2004-07-15 | 2009-11-03 | L'oréal | Shine-enhancing film formers |
EP1743626A1 (en) * | 2005-07-13 | 2007-01-17 | L'Oréal | Skin make-up composition comprising a resin |
ES2530853T3 (en) * | 2005-07-13 | 2015-03-06 | Oreal | High strength lip makeup composition comprising a low molecular weight resin |
-
1976
- 1976-01-22 JP JP625576A patent/JPS5936603B2/en not_active Expired
Also Published As
Publication number | Publication date |
---|---|
JPS5290637A (en) | 1977-07-30 |
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