JPH06199640A - Hair cosmetics - Google Patents
Hair cosmeticsInfo
- Publication number
- JPH06199640A JPH06199640A JP34826792A JP34826792A JPH06199640A JP H06199640 A JPH06199640 A JP H06199640A JP 34826792 A JP34826792 A JP 34826792A JP 34826792 A JP34826792 A JP 34826792A JP H06199640 A JPH06199640 A JP H06199640A
- Authority
- JP
- Japan
- Prior art keywords
- hair
- acid
- chemical
- manufactured
- odor
- 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
Links
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q5/00—Preparations for care of the hair
- A61Q5/06—Preparations for styling the hair, e.g. by temporary shaping or colouring
-
- 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
-
- 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
- A61K8/58—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing atoms other than carbon, hydrogen, halogen, oxygen, nitrogen, sulfur or phosphorus
- A61K8/585—Organosilicon compounds
-
- 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
- A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
- A61K8/81—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
- A61K8/8141—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
- A61K8/8152—Homopolymers or copolymers of esters, e.g. (meth)acrylic acid esters; Compositions of derivatives of such polymers
-
- 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
- A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
- A61K8/81—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
- A61K8/8141—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
- A61K8/8158—Homopolymers or copolymers of amides or imides, e.g. (meth) acrylamide; Compositions of derivatives of such polymers
-
- 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
- A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
- A61K8/81—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
- A61K8/8164—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a carboxyl radical, and containing at least one other carboxyl radical in the molecule, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers, e.g. poly (methyl vinyl ether-co-maleic anhydride)
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)
- Compositions Of Macromolecular Compounds (AREA)
Abstract
(57)【要約】
【目的】 使用時に特有の刺激臭及び異臭がなく、毛髪
のセットを快適に行える毛髪化粧料の提供。
【構成】 本発明の毛髪化粧料は、(A)下記〔化1〕
の一般式(I)又は下記〔化2〕の一般式(II)で示さ
れる揮発性シリコーン油及び/又は沸点が0〜40℃の
揮発性炭化水素を少なくとも1種以上、(B)水溶性高
分子化合物及び(C)噴射剤を含有する。
【化1】
【化2】
(57) [Summary] [Purpose] To provide a hair cosmetic composition that does not have a peculiar irritating odor or a strange odor during use and can comfortably set hair. [Structure] The hair cosmetic composition of the present invention comprises (A)
Of the general formula (I) or the general formula (II) of the following [Chemical formula 2] and / or at least one volatile hydrocarbon having a boiling point of 0 to 40 ° C., (B) water-soluble It contains a polymer compound and (C) a propellant. [Chemical 1] [Chemical 2]
Description
【0001】[0001]
【産業上の利用分野】本発明は、ヘアスプレーとして用
いられる毛髪化粧料、詳しくは、使用時に特有の刺激臭
及び異臭がなく、毛髪のセットを快適に行える毛髪化粧
料に関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a hair cosmetic composition used as a hair spray, and more particularly to a hair cosmetic composition which does not have a peculiar irritating odor or a strange odor during use and can comfortably set hair.
【0002】[0002]
【従来の技術】従来、毛髪をセットする際に、整髪力や
セット保持力等を付与する目的でヘアスプレーが用いら
れてきた。該ヘアスプレーは、通常、毛髪固定用被膜形
成樹脂を主成分とし、他は溶剤であるエタノールと噴射
剤等で構成されている。2. Description of the Related Art Heretofore, a hair spray has been used for the purpose of imparting hair styling power and set holding power when setting hair. The hair spray usually comprises a hair-fixing film-forming resin as a main component, and the other components, such as ethanol as a solvent and a propellant.
【0003】[0003]
【発明が解決しようとする課題】上記ヘアスプレーは、
溶剤としてのエタノールと噴射剤とがスプレーされた時
に空気中に気化及び飛散し、それが使用者が感じる刺激
臭及び異臭となり問題となってきた。しかしながら、ヘ
アスプレーは、毛髪を固定し、スタイルを保持するには
極めて優れた性能を有しているため、広く消費者の中に
受け入れられてきた。現在では、この刺激臭及び異臭を
極力少なくするために、原料臭を少なくする、香料でマ
スキングを行う等の方法が行われてきているが、顕著な
効果はない。また、近年、無香料のヘアスプレーが市販
されているが、原料臭及びエタノールの刺激臭は一向に
低減されていないのが実状である。The above hair spray is
When ethanol as a solvent and a propellant are sprayed, they are vaporized and scattered in the air, which causes an irritating odor and a strange odor felt by the user, which has become a problem. However, hair sprays have gained wide acceptance among consumers due to their exceptional performance in fixing hair and retaining style. At present, in order to reduce the irritating odor and the offensive odor as much as possible, methods such as reducing the raw material odor and masking with a fragrance have been performed, but there is no remarkable effect. In recent years, fragrance-free hair sprays have been marketed, but the fact is that the raw material odor and the pungent odor of ethanol have not been reduced.
【0004】また、特開昭61−161214号公報に
は、特定の有機シリコーン樹脂、揮発性シリコーン油及
び噴射ガスを含有するヘアスプレーが記載されている
が、該ヘアスプレーは、毛髪に対して、良好なセット保
持力と、優れた光沢やなめらかさを付与することを目的
とするものであり、原料臭及びエタノールの刺激臭の抑
制について全く配慮されていない。Further, JP-A-61-161214 describes a hair spray containing a specific organic silicone resin, a volatile silicone oil and a propellant gas. The hair spray is applied to hair. The purpose is to impart good set holding power and excellent luster and smoothness, and no consideration is given to the suppression of the raw material odor and the pungent odor of ethanol.
【0005】従って、本発明の目的は、使用時に特有の
刺激臭及び異臭がなく、毛髪のセットを快適に行える毛
髪化粧料を提供することにある。Therefore, an object of the present invention is to provide a hair cosmetic composition which does not have a peculiar irritating odor or a strange odor when used and which can comfortably set hair.
【0006】[0006]
【課題を解決するための手段】本発明者らは、鋭意研究
を重ねた結果、特定の揮発性物質、特定の毛髪固定用被
膜形成樹脂及び液化ガス又は圧縮ガスを併用することに
より、上記目的を達成できると共に、ヘアスプレーとし
て重要な性能であるスプレー時の乾燥速度が著しく速く
なり、スプレーの使用感が向上し、且つセットが瞬時に
できるため、スタイルの保持力が持続できることを知見
した。Means for Solving the Problems As a result of intensive studies, the present inventors have found that the use of a specific volatile substance, a specific hair-fixing film-forming resin, and a liquefied gas or a compressed gas can achieve the above-mentioned object. In addition to achieving the above, it was found that the drying speed at the time of spraying, which is an important performance as a hair spray, is remarkably increased, the usability of the spray is improved, and the setting can be done instantly, so that the style holding power can be maintained.
【0007】本発明は、上記知見に基づいてなされたも
ので、(A)下記〔化3〕の一般式(I)(前記〔化
1〕の一般式(I)と同じ)又は下記〔化4〕の一般式
(II)(前記〔化2〕の一般式(II)と同じ)で示され
る揮発性シリコーン油及び/又は沸点が0〜40℃の揮
発性炭化水素を少なくとも1種以上、(B)水溶性高分
子化合物及び(C)噴射剤を含有することを特徴とする
毛髪化粧料を提供するものである。The present invention has been made based on the above-mentioned findings. (A) The general formula (I) of the following [Chemical formula 3] (the same as the general formula (I) of the above [Chemical formula 1]) or the following 4] at least one volatile silicone oil represented by the general formula (II) (the same as the general formula (II) of [Chemical Formula 2]) and / or at least one volatile hydrocarbon having a boiling point of 0 to 40 ° C., A hair cosmetic comprising (B) a water-soluble polymer compound and (C) a propellant.
【0008】[0008]
【化3】 [Chemical 3]
【0009】[0009]
【化4】 [Chemical 4]
【0010】以下、本発明の毛髪化粧料について詳述す
る。The hair cosmetic composition of the present invention will be described in detail below.
【0011】本発明の(A)成分の前記一般式(I)で
示される揮発性シリコーン油(鎖状シリコーン)として
は、ヘキサメチルジシロキサン(m=0)又はオクタメ
チルトリシロキサン(m=1)が好ましく、また前記一
般式(II)で示される揮発性シリコーン油(環状シリコ
ーン)としては、ヘキサメチルシクロトリシロキサン
(n=3)又はオクタメチルシクロテトラシロキサン
(n=4)が好ましい。The volatile silicone oil (chain silicone) represented by the general formula (I) of the component (A) of the present invention is hexamethyldisiloxane (m = 0) or octamethyltrisiloxane (m = 1). ) Is preferable, and hexamethylcyclotrisiloxane (n = 3) or octamethylcyclotetrasiloxane (n = 4) is preferable as the volatile silicone oil (cyclic silicone) represented by the general formula (II).
【0012】また、本発明の(A)成分の揮発性炭化水
素としては、沸点が0〜40℃(好ましくは5〜40
℃)の炭化水素で、炭素数4〜6の直鎖状又は分岐状炭
化水素が好ましく、例えば、ネオペンタン(沸点9.5
℃)、イソペンタン(沸点27.9℃)、n−ペンタン
(沸点36.1℃)が挙げられる。The volatile hydrocarbon as the component (A) of the present invention has a boiling point of 0 to 40 ° C. (preferably 5 to 40).
C) hydrocarbons, preferably linear or branched hydrocarbons having 4 to 6 carbon atoms, such as neopentane (boiling point 9.5).
C.), isopentane (boiling point 27.9 ° C.), n-pentane (boiling point 36.1 ° C.).
【0013】本発明の(A)成分としては、上記揮発性
シリコーン油及び/又は上記揮発性炭化水素の少なくと
も1種以上が用いられる。As the component (A) of the present invention, at least one of the above volatile silicone oil and / or the above volatile hydrocarbon is used.
【0014】上記(A)成分の配合量は、毛髪化粧料中
に好ましくは0.01〜50重量%、特に好ましくは1
0〜40重量%である。The amount of the above-mentioned component (A) is preferably 0.01 to 50% by weight, and particularly preferably 1 in the hair cosmetic composition.
It is 0 to 40% by weight.
【0015】また、本発明の(B)成分の水溶性高分子
化合物としては、天然、半合成及び合成のいずれのもの
を用いてもよい。As the water-soluble polymer compound as the component (B) of the present invention, any of natural, semi-synthetic and synthetic compounds may be used.
【0016】天然の水溶性高分子化合物としては、例え
ば、アラビアガム、トラガカントガム、ガラクタン、グ
アガム、キャロブガム、カラヤガム、カラギーナン、ペ
クチン、カンテン、クインスシード(マルメロ)、グリ
チルリチン酸等の植物系高分子化合物、キサンタンガ
ム、デキストラン、サクシノグルカン、プルラン等の微
生物系高分子化合物、更には、ケラチン物質分解誘導体
等のタンパク質加水分解物系高分子化合物が挙げられ
る。Examples of natural water-soluble polymer compounds include botanical polymer compounds such as gum arabic, tragacanth gum, galactan, guar gum, carob gum, karaya gum, carrageenan, pectin, agar, quince seed (quince), and glycyrrhizic acid. Examples thereof include microbial polymer compounds such as xanthan gum, dextran, succinoglucan, and pullulan, and protein hydrolyzate polymer compounds such as keratin substance-degrading derivatives.
【0017】上記ケラチン物質分解誘導体は、ケラチン
物質を酸化分解するか、ケラチン物質を還元分解し、そ
のチオール基を化学修飾して得られる誘導体である。ケ
ラチン物質としては、例えば獣毛、毛髪、羽毛、爪、
角、蹄、鱗等が挙げられるが、就中、羊毛、毛髪及び羽
毛が特に好ましい。当該チオール基における誘導体とし
ては、下記〔化5〕に示すものが挙げられ、これらの中
でも、下記〔化6〕に示すものが特に好ましい。The keratin substance-decomposing derivative is a derivative obtained by oxidatively decomposing a keratin substance or reductively decomposing a keratin substance and chemically modifying its thiol group. Examples of the keratin substance include animal hair, hair, feathers, nails,
Horns, hoofs, scales and the like can be mentioned, with wool, hair and feathers being particularly preferred. Examples of the derivative in the thiol group include those shown in the following [Chemical formula 5], and among these, those shown in the following [Chemical formula 6] are particularly preferable.
【化5】 [Chemical 5]
【0018】[0018]
【化6】 [Chemical 6]
【0019】上記チオール基の化学修飾は、公知の手
段、例えば、N. H. Leon : Textile Progress 、第7
巻、1頁 (1975) 、大饗茂著「有機イオウ化合物」(化
学同人発行(1968))及び奥正巳著「高分子実験学講
座」12巻(共立出版発行(1957))に記載の手段に基
づいて行われる。The above-mentioned chemical modification of the thiol group can be carried out by known means, for example, NH Leon: Textile Progress, No. 7
Vol. 1, p. (1975), Shigeru Ohtsuga, "Organic Sulfur Compounds" (published by Kagaku Dojin (1968)) and Masami Oku, "Polymer Experimental Course" Volume 12 (published by Kyoritsu Publishing (1957)). It is done based on.
【0020】また、半合成の水溶性高分子化合物として
は、例えば、カルボキシメチルデンプン、メチルヒドロ
キシプロピルデンプン等のデンプン系高分子化合物、メ
チルセルロース、ニトロセルロース、エチルセルロー
ス、メチルヒドロキシプロピルセルロース、ヒドロキシ
エチルセルロース、セルロース硫酸ナトリウム、ヒドロ
キシプロピルセルロース、カルボキシメチルセルロース
ナトリウム(CMC)、結晶セルロース、セルロース末
等のセルロース系高分子化合物、アルギン酸ナトリウ
ム、アルギン酸プロピレングリコールエステル等のアル
ギン酸系高分子化合物が挙げられる。Examples of the semi-synthetic water-soluble polymer compound include starch polymer compounds such as carboxymethyl starch and methyl hydroxypropyl starch, methyl cellulose, nitrocellulose, ethyl cellulose, methyl hydroxypropyl cellulose, hydroxyethyl cellulose and cellulose. Examples thereof include cellulosic polymer compounds such as sodium sulfate, hydroxypropyl cellulose, sodium carboxymethyl cellulose (CMC), crystalline cellulose and cellulose powder, and alginate polymer compounds such as sodium alginate and propylene glycol alginate.
【0021】また、合成の水溶性高分子化合物として
は、以下の例が挙げられる。 (1)ポリビニルピロリドン系高分子化合物 例えば、ポリビニルピロリドン、及びビニルピロリドン
と酢酸ビニル、アルキルアミノアクリレート等との共重
合体等が挙げられ、市販品としては、ポリビニルピロリ
ドンとして、Luviskol K (BASF社製)、PVP K (GAF社
製) 等が挙げられ、ビニルピロリドンと酢酸ビニルとの
共重合体として、Luviskol VA (BASF 社製)、PVP/VA
(GAF 社製) 等が挙げられ、ビニルピロリドンと酢酸ビ
ニルとプロピオン酸ビニルとの共重合体として、Luvisk
ol VAP (BASF社製)等が挙げられ、ビニルピロリドンと
アルキルアミノアクリレートとの共重合体として、コポ
リマー845 (GAF 社製) 等が挙げられ、ビニルピロリド
ンとアルキルアミノアクリレートとビニルカプロラクタ
ムとの三元共重合体として、コポリマー VC-713 (GAF社
製)等が挙げられ、ビニルピロリドンとアクリル酸及び
メタクリル酸との共重合体として、Vem (Ban-Stalfort
社製)等が挙げられる。Further, examples of synthetic water-soluble polymer compounds include the following. (1) Polyvinylpyrrolidone-based polymer compounds For example, polyvinylpyrrolidone and copolymers of vinylpyrrolidone and vinyl acetate, alkylamino acrylate and the like can be mentioned. As a commercial product, as polyvinylpyrrolidone, Luviskol K (manufactured by BASF) ), PVP K (manufactured by GAF) and the like, and as a copolymer of vinylpyrrolidone and vinyl acetate, Luviskol VA (manufactured by BASF), PVP / VA
(Manufactured by GAF) and the like, and as a copolymer of vinylpyrrolidone, vinyl acetate and vinyl propionate, Luvisk
ol VAP (manufactured by BASF) and the like, and a copolymer of vinylpyrrolidone and an alkylaminoacrylate such as copolymer 845 (manufactured by GAF). A ternary compound of vinylpyrrolidone, an alkylaminoacrylate and vinylcaprolactam. Examples of the copolymer include copolymer VC-713 (manufactured by GAF) and the like, and as a copolymer of vinylpyrrolidone and acrylic acid and methacrylic acid, Vem (Ban-Stalfort
Manufactured by the company) and the like.
【0022】(2)酢酸ビニルエーテル系高分子化合物 例えば、メチルビニルエーテルと無水マレイン酸との共
重合体の低級アルキルハーフエステル等が挙げられ、市
販品としては、ガントレッツES-225、ES-335、ES-425、
SP-215 (GAF 社製) 等が挙げられる。(2) Vinyl acetate ether type polymer compound For example, a lower alkyl half ester of a copolymer of methyl vinyl ether and maleic anhydride and the like can be mentioned. Commercially available products are GANTREZ ES-225, ES-335, ES -425,
SP-215 (manufactured by GAF) and the like can be mentioned.
【0023】(3)酸性ポリ酢酸ビニル系高分子化合物 例えば、酢酸ビニルとクロトン酸等との共重合体等が挙
げられ、市販品としては、酢酸ビニルとクロトン酸との
共重合体として、レジン28−1310 (National Starch 社
製) 、ルビセットCA (BASF社製)等が挙げられ、酢酸ビ
ニルとクロトン酸とネオデカン酸ビニルとの三元重合体
として、レジン28-2930 (National Starch社製)等が挙
げられ、酢酸ビニルとクロトン酸とプロピオン酸ビニル
との三元共重合体として、ルビセット CAP (BASF社製)
等が挙げられ、酢酸ビニルとN−ビニル−5−メチル−
2−オキサゾリンとの共重合体として、Dewlex (Dow Ch
emical社製)等が挙げられる。(3) Acidic Polyvinyl Acetate Polymer Compound For example, a copolymer of vinyl acetate and crotonic acid may be mentioned. As a commercial product, a copolymer of vinyl acetate and crotonic acid may be used. 28-1310 (manufactured by National Starch), Rubiset CA (manufactured by BASF), and the like. As a terpolymer of vinyl acetate, crotonic acid, and vinyl neodecanoate, resin 28-2930 (manufactured by National Starch), etc. Rubiset CAP (manufactured by BASF) as a terpolymer of vinyl acetate, crotonic acid, and vinyl propionate.
And the like, vinyl acetate and N-vinyl-5-methyl-
As a copolymer with 2-oxazoline, Dewlex (Dow Ch
emical) and the like.
【0024】(4)酸性アクリル系高分子化合物 例えば、アクリル酸及び/又はメタクリル酸とアクリル
酸アルキルエステル及び/又はメタクリル酸アルキルエ
ステルとの共重合体、及びアクリル酸とアクリル酸アル
キルエステルとN−アルキルアクリルアミドとの共重合
体等が挙げられ、市販品としては、プラスサイズ L-53P
(瓦応化学(株)製)、ウルトラホールド8 (BASF社
製)等が挙げられる。(4) Acidic acrylic polymer compound For example, a copolymer of acrylic acid and / or methacrylic acid and acrylic acid alkyl ester and / or methacrylic acid alkyl ester, and acrylic acid and acrylic acid alkyl ester and N- Copolymers with alkyl acrylamide, etc. are listed as commercial products, plus size L-53P
(Kawao Chemical Co., Ltd.), Ultrahold 8 (manufactured by BASF) and the like.
【0025】(5)両性アクリル系高分子化合物 例えば、ジアルキルアミノエチルメタクリレート、ジア
ルキルアミノエチルアクリレート、ダイアセトンアクリ
ルアミド等とアクリル酸、メタクリル酸、アクリル酸ア
ルキルエステル、メタクリル酸アルキルエステル等とを
共重合し、ハロゲン化酢酸で両性化した化合物等が挙げ
られ、市販品としては、ユカフォーマーAM75 、R205、A
M75S/SM、(三菱油化(株)製)等が挙げられる。ま
た、アクリル酸ヒドロキシプロピルとメタクリル酸ブチ
ルアミノエチル及びアクリル酸オクチルアミドとの三元
共重合体等も挙げられ、市販品としては、アンフォマー
(AMPHOMER)28-4910、LV-71 (National Starch社製)等
が挙げられる。(5) Amphoteric acrylic polymer compound For example, dialkylaminoethyl methacrylate, dialkylaminoethyl acrylate, diacetone acrylamide, etc. are copolymerized with acrylic acid, methacrylic acid, acrylic acid alkyl ester, methacrylic acid alkyl ester, etc. , A compound ampholyzed with a halogenated acetic acid, and the like, and commercially available products include Yucaformer AM75, R205, A
M75S / SM, manufactured by Mitsubishi Petrochemical Co., Ltd., and the like. In addition, a terpolymer such as hydroxypropyl acrylate and butylaminoethyl methacrylate and octylamide acrylic acid may also be mentioned. As commercial products, Amphomer (AMPHOMER) 28-4910, LV-71 (National Starch Co. ) And the like.
【0026】(6)塩基性アクリル系高分子化合物 例えば、アルキルアクリルアミド、アクリレート、アル
キルアミノアルキルアクリルアミド及びポリエチレング
リコールメタクリレートの共重合体〔例えば、特開平2
−180911号公報に記載の水溶性高分子化合物〕等
が挙げられる。(6) Basic acrylic polymer compound For example, a copolymer of alkyl acrylamide, acrylate, alkylaminoalkyl acrylamide and polyethylene glycol methacrylate [see, for example, JP-A-2
Water-soluble polymer compounds described in JP-A-180911] and the like.
【0027】尚、上記水溶性高分子化合物の内、酸基を
もった高分子化合物については、洗髪性の向上及び感触
の点から、酸基の一部又は全部を中和することが好まし
い。中和に使用するアルカリとしては、特に制約はな
く、高分子化合物中の酸基をナトリウム、カリウム等の
アルカリ金属塩;アンモニウム塩あるいはエタノールア
ミン、ジエタノールアミン、トリエタノールアミン、2
−アミノ−2−メチルプロパノール、2−アミノ−2−
メチル−1,3−プロパンジオール、アミノメルカプト
プロパンジオール、トリイソプロパノールアミン、グリ
シン、ヒスチジン、アルギニン等の有機塩基塩とするこ
とができる。これらの内、特に2−アミノ−2−メチル
プロパノール、2−アミノ−2−メチル−1,3−プロ
パンジオールの塩が好ましい。また、塩基性をもった高
分子化合物についても同様に塩基性基の一部又は全部を
中和することが好ましい。中和に使用する酸としては、
特に制約はないが、無機酸としては、例えば、塩酸、硫
酸、リン酸等が好ましく、有機酸としては、例えば、酢
酸、乳酸、グリコール酸、ジメチロールプロピオン酸、
酒石酸、クエン酸、マレイン酸、リンゴ酸等が好まし
い。Among the above water-soluble polymer compounds, it is preferable to neutralize a part or all of the acid groups of the polymer compound having an acid group, from the viewpoints of improving the washability and feeling. The alkali used for neutralization is not particularly limited, and the acid group in the polymer compound is an alkali metal salt such as sodium or potassium; ammonium salt or ethanolamine, diethanolamine, triethanolamine, 2
-Amino-2-methylpropanol, 2-amino-2-
It can be an organic base salt such as methyl-1,3-propanediol, aminomercaptopropanediol, triisopropanolamine, glycine, histidine, and arginine. Of these, salts of 2-amino-2-methylpropanol and 2-amino-2-methyl-1,3-propanediol are particularly preferable. Similarly, it is preferable to neutralize a part or all of the basic groups in a basic polymer compound. As the acid used for neutralization,
There is no particular limitation, but as the inorganic acid, for example, hydrochloric acid, sulfuric acid, phosphoric acid and the like are preferable, and as the organic acid, for example, acetic acid, lactic acid, glycolic acid, dimethylolpropionic acid,
Tartaric acid, citric acid, maleic acid, malic acid and the like are preferable.
【0028】本発明の(B)成分としては、上記水溶性
高分子化合物の中から、1種又は2種以上が適宜選択さ
れ用いられるが、上記水溶性高分子化合物の中でも、特
に好ましいものとしては、以下のものが挙げられる。As the component (B) of the present invention, one kind or two or more kinds are appropriately selected and used from the above water-soluble polymer compounds, and among the above water-soluble polymer compounds, particularly preferable ones are used. Are as follows.
【0029】酢酸ビニルエーテル系高分子化合物とし
て、例えば、メチルビニルエーテルと無水マレイン酸と
の共重合体の低級アルキルハーフエステル〔例えば、ガ
ントレッツES-225(GAF 社製)〕が挙げられ、両性アク
リル系高分子化合物として、例えば、(メタ)アクリル
酸エステルとカルボキシベタインジメチルアミノエチル
メタクリル酸エステルとの共重合体〔例えば、ユカフォ
ーマー AM75(三菱油化(株)製)〕が挙げられ、酸性ア
クリル系高分子化合物として、例えば、アクリル酸エス
テルとメタクリル酸及びアクリル酸との共重合体〔例え
ば、プラサイズ L-53D(瓦応化学(株)製)〕が挙げら
れ、塩基性アクリル系高分子化合物として、アルキルア
クリルアミド、アクリレート、アルキルアミノアルキル
アクリルアミド及びポリエチレングリコールメタクリレ
ートの共重合体〔例えば、特開平2−180911号公
報に記載の水溶性高分子化合物〕等が挙げられる。Examples of the vinyl acetate-based polymer compound include a lower alkyl half ester of a copolymer of methyl vinyl ether and maleic anhydride [for example, GANTREZ ES-225 (manufactured by GAF)]. Examples of the molecular compound include a copolymer of (meth) acrylic acid ester and carboxybetaine dimethylaminoethyl methacrylic acid ester [for example, Yukaformer AM75 (manufactured by Mitsubishi Yuka Co., Ltd.)], and acidic acrylic polymer Examples of the compound include a copolymer of acrylic acid ester, methacrylic acid, and acrylic acid [for example, PLASIZE L-53D (manufactured by Gao Kagaku Co., Ltd.)], and as the basic acrylic polymer compound, Alkyl acrylamide, acrylate, alkylaminoalkyl acrylamide and polyethylene Examples thereof include copolymers of lenglycol methacrylate [eg, water-soluble polymer compounds described in JP-A-2-180911].
【0030】上記(B)成分の配合量は、毛髪化粧料中
に好ましくは0.1〜20重量%、特に好ましくは5〜
10重量%である。The content of the above-mentioned component (B) in the hair cosmetic is preferably 0.1 to 20% by weight, particularly preferably 5 to 5.
It is 10% by weight.
【0031】また、本発明の(C)成分の噴射剤として
は、プロパン、n−ブタン、i−ブタン等を主成分とす
る液化石油ガス(LPG)等のハイドロカーボン類、ジ
メチルエーテル、メチルエチルエーテル、ジエチルエー
テル等のエーテル類である液化ガス、及びCO2 、
N2 、N2 O等の圧縮ガスが挙げられる。これらの噴射
剤は1種又は2種以上を混合して使用してもよく、その
配合量は、毛髪化粧料中に好ましくは0.5〜70重量
%、特に好ましくは10〜60重量%である。As the propellant of the component (C) of the present invention, hydrocarbons such as liquefied petroleum gas (LPG) containing propane, n-butane, i-butane, etc. as main components, dimethyl ether, methyl ethyl ether. , A liquefied gas that is an ether such as diethyl ether, and CO 2 ,
Compressed gas N 2, N 2 O, and the like. These propellants may be used alone or in admixture of two or more, and the compounding amount thereof is preferably 0.5 to 70% by weight, particularly preferably 10 to 60% by weight in the hair cosmetic composition. is there.
【0032】尚、本発明の毛髪化粧料には、上記(A)
〜(C)成分の相溶性を高めるために溶媒を用いること
ができ、好適な溶媒としては、炭素数1〜4の直鎖又は
分岐のアルコール(好ましくはエタノール)及び/又は
水等を挙げることができる。上記溶媒の配合量は、毛髪
化粧料中に好ましくは1〜55重量%、より好ましくは
3〜50重量%である。The hair cosmetic composition of the present invention includes the above (A).
~ A solvent can be used to increase the compatibility of the components (C), and suitable solvents include linear or branched alcohols having 1 to 4 carbon atoms (preferably ethanol) and / or water. You can The content of the above solvent in the hair cosmetic is preferably 1 to 55% by weight, more preferably 3 to 50% by weight.
【0033】また、本発明の毛髪化粧料には、その使用
目的に応じて本発明の効果を損なわない範囲で、香料、
界面活性剤(アニオン、ノニオン、カチオン)、起泡
剤、安定剤、防腐剤、顔料、染料、増粘剤、乳化剤、高
級脂肪族アルコール、ワックス、ふけ抑制剤、殺菌剤、
還元剤、薬剤、紫外線吸収剤、生薬抽出物、色素、分散
剤、流動パラフィン、スクワラン、ラノリン誘導体、高
級アルコール、各種エステル油、シリコーン油、ポリア
ルキレングリコール、ポリエーテル及びそのカルボン酸
オリゴエステル化合物、テルペン系炭化水素等に代表さ
れる油剤等の通常使用される毛髪化粧料の構成成分を全
て添加し得る。In addition, the hair cosmetic composition of the present invention contains a fragrance, depending on the purpose of use, within a range not impairing the effects of the present invention.
Surfactants (anions, nonions, cations), foaming agents, stabilizers, preservatives, pigments, dyes, thickeners, emulsifiers, higher aliphatic alcohols, waxes, dandruff inhibitors, bactericides,
Reducing agents, drugs, UV absorbers, crude drug extracts, pigments, dispersants, liquid paraffin, squalane, lanolin derivatives, higher alcohols, various ester oils, silicone oils, polyalkylene glycols, polyethers and their carboxylic acid oligoester compounds, All the components of commonly used hair cosmetics such as oil agents typified by terpene hydrocarbons can be added.
【0034】[0034]
【実施例】以下に、本発明を実施例により具体的に説明
するが、本発明はこれらに限定されるものではない。EXAMPLES The present invention will be described below in greater detail by giving Examples, but the present invention is not limited thereto.
【0035】実施例1 下記〔表1〕に示す組成の毛髪化粧料(本発明品1〜
6)を下記製法によりそれぞれ製造した。また、これら
の毛髪化粧料の内、本発明品1〜3について、市販スプ
レー(A)を対照として匂い、セット力及び乾き速度を
下記方法により評価した。その結果を下記〔表2〕に示
す。Example 1 Hair cosmetics having the composition shown in the following [Table 1]
6) was manufactured by the following manufacturing method. Further, among these hair cosmetics, the products 1 to 3 of the present invention were evaluated for odor, setting force and drying speed by the following methods with a commercially available spray (A) as a control. The results are shown in [Table 2] below.
【0036】〔製法〕まず、噴射剤以外の成分を混合あ
るいは溶解して原液とし、次いで、原液を耐圧容器に入
れ、更に、噴射剤を添加して毛髪化粧料を得る。[Manufacturing Method] First, components other than the propellant are mixed or dissolved to prepare a stock solution, and then the stock solution is placed in a pressure resistant container, and further the propellant is added to obtain a hair cosmetic composition.
【0037】〔匂いの評価方法〕スプレー時の匂いの強
さ、スプレー時の刺激臭及びスプレー後の残香の強さを
下記基準により評価する。[Odor Evaluation Method] The strength of the odor during spraying, the pungent odor during spraying, and the strength of residual scent after spraying are evaluated according to the following criteria.
【0038】匂い(匂いの強さ、刺激臭及び残香の強さ)の評価基準 ◎:たいへん弱い。 ○:弱い。 ○〜△:普通。 △:やや強い。 ×:強い。 Odor (strength of odor, irritating odor, and strength of residual odor) evaluation criteria A : Very weak ○: Weak. ○ to △: Normal. Δ: Slightly strong X: Strong.
【0039】〔セット力の評価方法(セット保持率)〕
長さ18cm、重さ1.5g の毛束を水でぬらし、直径2
cmのロッドに巻いて自然乾燥させる。乾燥後、カールの
ついた毛髪からロッドをはずし、15cmの距離から毛髪
化粧料を噴霧する。乾燥後、恒温・恒湿箱(20℃、9
8%RH)に30分間つるし、カールの伸びを観察し、
セット保持率(%)を判定する。尚、毛髪化粧料を毛髪
に噴霧しなかった場合(ブランク)のセット保持率は3
5%であった。[Evaluation method of set force (set holding ratio)]
Wet a hair bundle that is 18 cm long and weighs 1.5 g and wet it to a diameter of 2
Wrap it on a cm rod and let it air dry. After drying, remove the rod from the curled hair and spray the hair cosmetic from a distance of 15 cm. After drying, constant temperature and humidity box (20 ℃, 9
8% RH) for 30 minutes, observe the curl elongation,
Determine the set retention rate (%). The set retention rate when the hair cosmetic was not sprayed on the hair (blank) was 3
It was 5%.
【0040】〔乾き速度の評価方法〕毛髪を植え込んだ
人頭モデル(ウィッグ)をセットし、15cmの距離から
毛髪化粧料を噴霧し、噴霧直後から一定時間の間隔で乾
きを官能評価する。[Evaluation Method of Drying Speed] A human head model (wig) in which hair is implanted is set, hair cosmetics are sprayed from a distance of 15 cm, and dryness is sensory evaluated immediately after spraying at regular time intervals.
【0041】乾きの評価基準 ◎:速い。 ○:やや速い。 ○〜△:普通。 △:やや遅い。 ×:遅い。 Evaluation Criteria for Dryness A : Fast. ○: Slightly fast. ○ to △: Normal. Δ: Slightly slow. X: Slow.
【0042】[0042]
【表1】 [Table 1]
【0043】上記〔表1〕における*1〜*8は次の通
りである。 *1 ヘキサメチルジシロキサン *2 オクタメチルトリシロキサン *3 オクタメチルシクロテトラシロキサン *4 下記〔化7〕の式で示される両性アクリル系高分
子化合物(National Starch社製) *5 下記〔化8〕の式で示される両性アクリル系高分
子化合物(三菱油化(株)製) *6 下記〔化9〕の式で示される酢酸ビニルエーテル
系高分子化合物(GAF 社製) *7 特開平2−180911号公報に記載の水溶性高
分子化合物 *8 α−モノイソステアリルグリセリルエーテル* 1 to * 8 in the above [Table 1] are as follows. * 1 Hexamethyldisiloxane * 2 Octamethyltrisiloxane * 3 Octamethylcyclotetrasiloxane * 4 Amphoteric acrylic polymer compound represented by the following formula [Chemical formula 7] (manufactured by National Starch) * 5 The following [Chemical formula 8] Amphoteric acrylic polymer compound represented by the formula (manufactured by Mitsubishi Yuka Co., Ltd.) * 6 Vinyl acetate ether polymer compound represented by the formula [Chem. 9] below (manufactured by GAF) * 7 JP-A-2-180911 -Soluble polymer compounds described in Japanese Patent Publication No. 8 α-monoisostearyl glyceryl ether
【0044】[0044]
【化7】 [Chemical 7]
【0045】[0045]
【化8】 [Chemical 8]
【0046】[0046]
【化9】 [Chemical 9]
【0047】[0047]
【表2】 [Table 2]
【0048】上記〔表2〕に示す結果から明らかなよう
に、本発明品は何れも、使用時に特有の刺激臭及び異臭
が殆どなく、しかもセット力及び乾き速度も良好であ
る。As is clear from the results shown in Table 2 above, all of the products of the present invention have almost no peculiar irritating odor and off-flavor during use, and also have good setting power and drying speed.
【0049】[0049]
【発明の効果】本発明の毛髪化粧料は、使用時に特有の
刺激臭及び異臭がなく、毛髪のセットを快適に行えると
共に、ヘアスプレーとして重要な性能であるスプレー時
の乾燥速度が著しく速くなり、スプレーの使用感が向上
し、且つセットが瞬時にできるため、スタイルの保持力
が持続できるものである。EFFECTS OF THE INVENTION The hair cosmetic composition of the present invention has no irritating odor or offensive odor peculiar to the hair when used, and allows the hair to be comfortably set, and the drying speed at the time of spraying, which is an important performance as a hair spray, is significantly increased. Since the spray feel is improved and the setting can be done instantly, the retention of style can be maintained.
─────────────────────────────────────────────────────
─────────────────────────────────────────────────── ───
【手続補正書】[Procedure amendment]
【提出日】平成5年1月29日[Submission date] January 29, 1993
【手続補正1】[Procedure Amendment 1]
【補正対象書類名】明細書[Document name to be amended] Statement
【補正対象項目名】0002[Name of item to be corrected] 0002
【補正方法】変更[Correction method] Change
【補正内容】[Correction content]
【0002】[0002]
【従来の技術】従来、毛髪をセットする際に、整髪力や
セット保持力等を付与する目的でヘアスプレーが用いら
れてきた。該ヘアスプレーは、通常、毛髪固定用被膜形
成樹脂を主成分とし、他は感触向上の為の油剤及び溶剤
であるエタノールと噴射剤等で構成されている。2. Description of the Related Art Heretofore, a hair spray has been used for the purpose of imparting hair styling power and set holding power when setting hair. The hair spray usually contains a hair-fixing film-forming resin as a main component, and the other components are composed of an oil agent for improving the feel , ethanol as a solvent and a propellant.
【手続補正2】[Procedure Amendment 2]
【補正対象書類名】明細書[Document name to be amended] Statement
【補正対象項目名】0025[Name of item to be corrected] 0025
【補正方法】変更[Correction method] Change
【補正内容】[Correction content]
【0025】(5)両性アクリル系高分子化合物 例えば、ジアルキルアミノエチルメタクリレート、ジア
ルキルアミノエチルアクリレート、ダイアセトンアクリ
ルアミド等とアクリル酸、メタクリル酸、アクリル酸ア
ルキルエステル、メタクリル酸アルキルエステル等とを
共重合し、ハロゲン化酢酸で両性化した化合物等が挙げ
られ、市販品としては、ユカフォーマーAM75/R205、AM7
5S/SM、(三菱油化(株)製)等が挙げられる。また、
アクリル酸ヒドロキシプロピルとメタクリル酸ブチルア
ミノエチル及びアクリル酸オクチルアミドとの三元共重
合体等も挙げられ、市販品としては、アンフォマー(AM
PHOMER)28-4910、LV-71 (National Starch社製)等が挙
げられる。(5) Amphoteric acrylic polymer compound For example, dialkylaminoethyl methacrylate, dialkylaminoethyl acrylate, diacetone acrylamide, etc. are copolymerized with acrylic acid, methacrylic acid, acrylic acid alkyl ester, methacrylic acid alkyl ester, etc. , A compound ampholyzed with a halogenated acetic acid, and the like, and commercially available products include Yucaformer AM75 / R205 and AM7.
5S / SM, manufactured by Mitsubishi Petrochemical Co., Ltd., and the like. Also,
Examples include terpolymers of hydroxypropyl acrylate, butylaminoethyl methacrylate, and octylamide acrylate. Commercial products include amphomer (AM
PHOMER) 28-4910, LV-71 (manufactured by National Starch) and the like.
【手続補正3】[Procedure 3]
【補正対象書類名】明細書[Document name to be amended] Statement
【補正対象項目名】0029[Name of item to be corrected] 0029
【補正方法】変更[Correction method] Change
【補正内容】[Correction content]
【0029】酢酸ビニルエーテル系高分子化合物とし
て、例えば、メチルビニルエーテルと無水マレイン酸と
の共重合体の低級アルキルハーフエステル〔例えば、ガ
ントレッツES-225(GAF 社製)〕が挙げられ、両性アク
リル系高分子化合物として、例えば、(メタ)アクリル
酸エステルとカルボキシベタインジメチルアミノエチル
メタクリル酸エステルとの共重合体〔例えば、ユカフォ
ーマー AM75(三菱油化(株)製)〕が挙げられ、酸性ア
クリル系高分子化合物として、例えば、アクリル酸エス
テルとメタクリル酸及びアクリル酸との共重合体〔例え
ば、プラサイズ L-53P(瓦応化学(株)製)〕が挙げら
れ、塩基性アクリル系高分子化合物として、アルキルア
クリルアミド、アクリレート、アルキルアミノアルキル
アクリルアミド及びポリエチレングリコールメタクリレ
ートの共重合体〔例えば、特開平2−180911号公
報に記載の水溶性高分子化合物〕等が挙げられる。Examples of the vinyl acetate-based polymer compound include a lower alkyl half ester of a copolymer of methyl vinyl ether and maleic anhydride [for example, GANTREZ ES-225 (manufactured by GAF)]. Examples of the molecular compound include a copolymer of (meth) acrylic acid ester and carboxybetaine dimethylaminoethyl methacrylic acid ester [for example, Yukaformer AM75 (manufactured by Mitsubishi Yuka Co., Ltd.)], and acidic acrylic polymer Examples of the compound include a copolymer of acrylic acid ester, methacrylic acid, and acrylic acid [for example, PLASIZE L-5 3P (manufactured by Gao Kagaku Co., Ltd.)], which is a basic acrylic polymer compound. , Alkyl acrylamides, acrylates, alkylaminoalkyl acrylamides and polyesters A copolymer of glycol methacrylate [for example, water-soluble polymer compound described in JP-A-2-180911], and the like.
【手続補正4】[Procedure amendment 4]
【補正対象書類名】明細書[Document name to be amended] Statement
【補正対象項目名】0031[Correction target item name] 0031
【補正方法】変更[Correction method] Change
【補正内容】[Correction content]
【0031】また、本発明の(C)成分の噴射剤として
は、プロパン、n−ブタン、i−ブタン等を主成分とす
る液化石油ガス(LPG)等のハイドロカーボン類、ジ
メチルエーテル、メチルエチルエーテル、ジエチルエー
テル等のエーテル類である液化ガス、及びCO2 、
N2 、N2 O等の圧縮ガスが挙げられる。これらの噴射
剤は1種又は2種以上を混合して使用してもよく、その
配合量は、液化ガスの場合は毛髪化粧料中に好ましくは
30〜70重量%、特に好ましくは40〜60重量%で
あり、また圧縮ガスの場合は毛髪化粧料中に好ましくは
0.1〜10重量%、特に好ましくは0.3〜5重量%
である。 As the propellant of the component (C) of the present invention, hydrocarbons such as liquefied petroleum gas (LPG) containing propane, n-butane, i-butane, etc. as main components, dimethyl ether, methyl ethyl ether. , A liquefied gas that is an ether such as diethyl ether, and CO 2 ,
Compressed gas N 2, N 2 O, and the like. These propellants may be used alone or in admixture of two or more, and in the case of liquefied gas , the blending amount is preferably in the hair cosmetic composition.
30-70% by weight, particularly preferably Ri <br/> Ah at 40 to 60 wt%, and if the compressed gas is preferably in the hair cosmetic composition
0.1 to 10% by weight, particularly preferably 0.3 to 5% by weight
Is.
Claims (1)
下記〔化2〕の一般式(II)で示される揮発性シリコー
ン油及び/又は沸点が0〜40℃の揮発性炭化水素を少
なくとも1種以上、(B)水溶性高分子化合物及び
(C)噴射剤を含有することを特徴とする毛髪化粧料。 【化1】 【化2】 1. A volatile silicone oil represented by the general formula (I) of the following [Chemical formula 1] or the general formula (II) of the following [Chemical formula 2] and / or a volatile substance having a boiling point of 0 to 40 ° C. A hair cosmetic comprising at least one hydrocarbon, (B) a water-soluble polymer compound, and (C) a propellant. [Chemical 1] [Chemical 2]
Priority Applications (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP34826792A JPH06199640A (en) | 1992-12-28 | 1992-12-28 | Hair cosmetics |
| DE9318715U DE9318715U1 (en) | 1992-12-28 | 1993-12-07 | Hair care products |
| DE19934341652 DE4341652A1 (en) | 1992-12-28 | 1993-12-07 | Hairspray having reduced unpleasant odour - contg propellant(s), high molecular wt cpd(s) and volatile silicones and/or low b.pt. hydrocarbon |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP34826792A JPH06199640A (en) | 1992-12-28 | 1992-12-28 | Hair cosmetics |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH06199640A true JPH06199640A (en) | 1994-07-19 |
Family
ID=18395886
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP34826792A Pending JPH06199640A (en) | 1992-12-28 | 1992-12-28 | Hair cosmetics |
Country Status (2)
| Country | Link |
|---|---|
| JP (1) | JPH06199640A (en) |
| DE (2) | DE4341652A1 (en) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2009513732A (en) * | 2003-07-08 | 2009-04-02 | ロレアル | Fragrance composition |
| US8440211B2 (en) | 2003-04-04 | 2013-05-14 | L'oreal S.A. | Cosmetic composition comprising a volatile fatty phase |
| WO2017099158A1 (en) * | 2015-12-11 | 2017-06-15 | 花王株式会社 | Hair cosmetic |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE19702156C1 (en) * | 1997-01-22 | 1998-08-06 | Wella Ag | Hair styling product giving good elasticity, bounce and shininess |
| FR2853244B1 (en) * | 2003-04-04 | 2008-11-07 | Oreal | COSMETIC COMPOSITION COMPRISING A VOLATILE FATTY PHASE |
| FR2853227B1 (en) * | 2003-04-04 | 2009-05-08 | Oreal | COSMETIC COMPOSITION COMPRISING A VOLATILE FATTY PHASE |
| FR2857260A1 (en) * | 2003-07-08 | 2005-01-14 | Oreal | A perfume composition comprising as a solvent a mixture of polydimethylsiloxanes comprising 30 wt.% hexamethyldisiloxane and 70 wt.% octamethyltrisiloxane |
| DE102007048290A1 (en) * | 2007-10-08 | 2009-04-09 | Henkel Ag & Co. Kgaa | Use of cyclic polydimethylsiloxanes to create a matte effect |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB2132653B (en) * | 1982-12-07 | 1985-12-18 | Dow Corning | Hair treatment compositions |
| EP0116207A3 (en) * | 1982-12-15 | 1986-03-12 | Beecham Group Plc | Cosmetic formulation |
-
1992
- 1992-12-28 JP JP34826792A patent/JPH06199640A/en active Pending
-
1993
- 1993-12-07 DE DE19934341652 patent/DE4341652A1/en not_active Withdrawn
- 1993-12-07 DE DE9318715U patent/DE9318715U1/en not_active Expired - Lifetime
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8440211B2 (en) | 2003-04-04 | 2013-05-14 | L'oreal S.A. | Cosmetic composition comprising a volatile fatty phase |
| JP2009513732A (en) * | 2003-07-08 | 2009-04-02 | ロレアル | Fragrance composition |
| WO2017099158A1 (en) * | 2015-12-11 | 2017-06-15 | 花王株式会社 | Hair cosmetic |
| JP2017109994A (en) * | 2015-12-11 | 2017-06-22 | 花王株式会社 | Hair cosmetics |
Also Published As
| Publication number | Publication date |
|---|---|
| DE9318715U1 (en) | 1994-04-28 |
| DE4341652A1 (en) | 1994-06-30 |
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