JPH0454116A - Hair spray composition - Google Patents

Hair spray composition

Info

Publication number
JPH0454116A
JPH0454116A JP16111090A JP16111090A JPH0454116A JP H0454116 A JPH0454116 A JP H0454116A JP 16111090 A JP16111090 A JP 16111090A JP 16111090 A JP16111090 A JP 16111090A JP H0454116 A JPH0454116 A JP H0454116A
Authority
JP
Japan
Prior art keywords
hair
group
polymer compound
formula
spray composition
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
JP16111090A
Other languages
Japanese (ja)
Inventor
Hideyuki Nakazawa
中沢 秀幸
Hideo Kurokawa
黒川 秀雄
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.)
Lion Corp
Original Assignee
Lion Corp
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 Lion Corp filed Critical Lion Corp
Priority to JP16111090A priority Critical patent/JPH0454116A/en
Publication of JPH0454116A publication Critical patent/JPH0454116A/en
Pending legal-status Critical Current

Links

Abstract

PURPOSE:To obtain a hair spray composition containing a polymer compound for fixing hair, having low corrosiveness to metal containers, having excellent antistatic effects on hair, without causing choking in use, by blending a polymer compound for fixing hair with a specific guanidine derivative or a salt thereof. CONSTITUTION:A polymer compound for fixing hair is blended with one or more selected from a guanidine derivative shown by the formula (R<1> is 1-22C alkyl or alkenyl; A is 1-10C alkylene or alkenylene; m is 0 or 1; n is 1-5) containing an amide group in the molecule and a salt thereof. The amount of the derivative blended is not particularly limited and is preferably 0.01-5 %, especially 0.02-3% based on the whole amount. A propellant such as LPG or halogenated hydrocarbon is used in the composition.

Description

【発明の詳細な説明】 〔産業上の利用分野〕 本発明は毛髪固定用高分子化合物を含有するヘアスプレ
ー組成物に関し、更に詳しくは、毛髪の帯電防止効果に
優れ、使用時にムセを生じることがなく、金属容器腐食
性の低いヘアスプレー組成物に関する。
[Detailed Description of the Invention] [Industrial Application Field] The present invention relates to a hair spray composition containing a hair fixing polymer compound, and more specifically, it has an excellent antistatic effect on hair and does not cause frizz when used. The present invention relates to a hairspray composition that is free of corrosion and has low corrosion resistance to metal containers.

〔従来の技術及び発明が解決しようとする課題〕従来、
セット維持効果をもった毛髪固定用高分子化合物を含む
ヘアスプレー組成物が種々提案されているが、毛髪を固
定し、長時間セントを維持するためには、毛髪の帯電を
防ぐ必要がある。ここで、毛髪の帯電はブラッシング等
によって引き起こされるもので、特にパーマ等で傷んだ
毛髪では帯電しやすい。また、毛髪の根元より先端部分
で風化による損傷が激しいため、静電気を帯び易い。毛
髪繊維が強く帯電している場合には、強いセント力を持
っているヘアスプレーを用いても、毛髪繊維間の静電気
的反発のために十分なセント効果を得ることができない
。特に、帯電の激しい先端部分では毛先のハネなどを生
じ、セント維持の支障となり易い。
[Problems to be solved by conventional techniques and inventions] Conventionally,
Various hair spray compositions containing hair-fixing polymer compounds that have a set-maintaining effect have been proposed, but in order to fix the hair and maintain the condition for a long time, it is necessary to prevent the hair from becoming electrostatically charged. Here, electrification of hair is caused by brushing or the like, and hair that has been damaged by a perm or the like is particularly susceptible to electrification. Additionally, the tips of the hair are more likely to be charged with static electricity because they are more likely to be damaged by weathering than the roots. If the hair fibers are strongly charged, even if a hairspray having a strong centrifugal force is used, a sufficient centrifugal effect cannot be obtained due to electrostatic repulsion between the hair fibers. Particularly, the tips of the bristles, which are heavily charged, tend to cause springiness, which can be a hindrance to maintaining cents.

このような問題を解決するための方法としては、従来、
ヘアスプレー組成物にジアルキルジメチルアンモニウム
クロライド、アルキルトリメチルアンモニウムクロライ
ドに代表される第4級アンモニウム塩を配合する方法が
知られている。しかしながら、第4級アンモニウム塩は
皮膚に対する刺激が強く、それを含むヘアスプレーより
噴霧された微粒子を吸入した場合、呼吸器粘膜を刺激し
、ムセを生じる原因となる。また、第4級アンモニウム
塩は金属腐食性があるため、それを含むヘアスプレー組
成物は金属容器を腐食しやすい。
Conventionally, methods to solve such problems are
A method is known in which a quaternary ammonium salt, typified by dialkyldimethylammonium chloride and alkyltrimethylammonium chloride, is blended into a hairspray composition. However, quaternary ammonium salts are highly irritating to the skin, and when fine particles sprayed from a hairspray containing them are inhaled, they irritate the respiratory mucous membranes and cause nausea. Furthermore, since quaternary ammonium salts are corrosive to metals, hairspray compositions containing them tend to corrode metal containers.

本発明は上記事情に鑑みなされたもので、優れた毛髪の
帯電防止効果を有し、また使用時にムセを生じさせるよ
うなこともなく、しかも金属容器腐食性の低いヘアスプ
レー組成物を提供することを目的とする。
The present invention has been made in view of the above circumstances, and provides a hair spray composition that has an excellent antistatic effect on hair, does not cause stiffness during use, and has low corrosion resistance to metal containers. The purpose is to

〔課題を解決するための手段〕[Means to solve the problem]

本発明者らは、上記目的を達成するため鋭意検討を重ね
た結果、毛髪固定用高分子化合物を含有するヘアスプレ
ー組成物に対し、下記一般式(1)(但し、式中R1は
炭素数1〜22の分岐状又は直鎖状のアルキル基又はア
ルケニル基であり、Aは炭素数1〜10の分岐状又は直
鎖状のアルキレン基又はアルケニレン基であり、mはO
又は1である。また、nは1〜5の整数である。)で示
される分子内にアミド基を持つグーアニジン誘導体やそ
れらの塩を配合した場合、帯電防止効果に優れ、かつ使
用時にムセを生じることもなく、また金属容器腐食性が
低いことを知見した。
As a result of intensive studies to achieve the above object, the present inventors have developed a hair spray composition containing a hair fixing polymer compound according to the following general formula (1) (wherein R1 is the number of carbon atoms). A is a branched or linear alkyl group or alkenyl group having 1 to 22 carbon atoms, A is a branched or linear alkylene group or alkenylene group having 1 to 10 carbon atoms, and m is O
Or 1. Moreover, n is an integer of 1-5. ) It has been found that when guanidine derivatives having an amide group in the molecule or their salts are blended, they have excellent antistatic effects, do not cause lumpiness during use, and are less corrosive to metal containers.

即ち、本出願人は、先に有効成分の毛髪への吸着性が高
く、毛髪に優れた柔軟性や保湿性を付与した毛髪化粧料
として、上記一般式(1)の化合物を有効成分とした毛
髪化粧料を提案した(特願昭63−320075号)が
、本発明者らは更に検討を進めた結果、上記一般式(1
)の化合物を毛髪固定用高分子化合物と共にヘアスプレ
ー組成物化した場合、スプレー容器となる金属容器を腐
食することがなく、また使用時にムセを生じさせること
もなく、しかも毛髪に対し優れた静電防止性を付与する
ことができることを見い出し、本発明をなすに至ったも
のである。
That is, the present applicant has previously developed a hair cosmetic in which the active ingredient is highly adsorbed to the hair and imparts excellent flexibility and moisturizing properties to the hair, using the compound of general formula (1) as an active ingredient. The present inventors proposed a hair cosmetic (Japanese Patent Application No. 63-320075), but as a result of further investigation, the above general formula (1)
) When the compound is made into a hair spray composition together with a hair-fixing polymer compound, it does not corrode the metal container used as a spray container, does not cause any stiffness during use, and has excellent electrostatic properties for hair. It has been discovered that it is possible to impart preventive properties, and the present invention has been completed.

以下、本発明につき更に詳述する。The present invention will be explained in more detail below.

本発明のヘアスプレー組成物に用いられる毛髪固定用高
分子化合物の種類に限定はなく、髪にセント力を付与す
るために従来用いられている高分子化合物であればいず
れのものも使用できるが、具体的には例えば下記(1)
〜(7)に示すものを挙げることができる。
The type of hair fixing polymer compound used in the hair spray composition of the present invention is not limited, and any polymer compound conventionally used to impart centrifugal force to hair can be used. , Specifically, for example, the following (1)
- (7) can be mentioned.

(1)メタクリル酸エステル共重合体の両性化物ここで
、上記メタクリル酸エステル共重合体の両性化物として
は下記式(A)、なかでも下記式(B)で表わされる構
成単位を主成分とし、これに共重合し得る単量体から誘
導される構成単位を適宜含み得る高分子化合物が好まし
い。
(1) Amphoterized product of methacrylic acid ester copolymer Here, the amphoteric product of the methacrylic acid ester copolymer has as a main component a structural unit represented by the following formula (A), especially the following formula (B), A polymer compound that can appropriately contain a structural unit derived from a monomer that can be copolymerized with the polymer compound is preferred.

・・・・・・ (A) (式中R,は炭素数1〜4のアルキレン基、Rよ及びR
1はそれぞれ炭素数1〜4のアルキル基、R4は炭素数
1〜24のアルキル基、炭素数4〜24のアルケニル基
、又はシクロアルキル基、m及びnはそれぞれ化合物(
A)を分子量10,000〜200,000とするため
の数である。) ・・・・・・ (B) (式中R4は上記と同し意味を示し、k及びEはそれぞ
れ化合物(B)を分子量50.000〜60,000に
するための数である。)これらの化合物として、三菱油
化社製のユカホーマーAM−75シリーズで販売されて
いる種々のグレードのもの、例えば204,205.2
06グレードのものが良好に使用できる。
...... (A) (In the formula, R is an alkylene group having 1 to 4 carbon atoms, R and R
1 is an alkyl group having 1 to 4 carbon atoms, R4 is an alkyl group having 1 to 24 carbon atoms, an alkenyl group having 4 to 24 carbon atoms, or a cycloalkyl group, m and n are each a compound (
This is the number for setting A) to have a molecular weight of 10,000 to 200,000. ) ...... (B) (In the formula, R4 has the same meaning as above, and k and E are numbers for making the compound (B) a molecular weight of 50,000 to 60,000, respectively.) These compounds include various grades of Yuka Homer AM-75 series manufactured by Mitsubishi Yuka Co., Ltd., such as 204 and 205.2.
06 grade can be used satisfactorily.

(2)メチルビニルエーテルと無水マレイン酸との共重
合体等の酸性ポリビニルエーテル系高分子化合物 (3)アクリル酸アルキルエステル−メタクリル酸アル
キルエステル共重合体等の酸性アクリル系高分子化合物 (4)ポリビニルピロリドンやビニルピロリドンと酢酸
ビニルとの共重合体等のポリビニルピロ・リドン系高分
子化合物 (5)酢酸ビニルとクロトン酸との共重合体等の酸性ポ
リ酢酸ビニル系高分子化合物 (6)ヒドロキシエチルセルロースをカチオン化したカ
チオン化セルロース (7)キチン、キトサンなどの天然高分子化合物なお、
これら高分子化合物の中で酸基を有するものは、適当な
アルカリ剤で中和して用いることが好ましい。また、こ
れら高分子化合物は1種を単独で用いてもよく、2種以
上を併用してもよい。
(2) Acidic polyvinyl ether polymer compounds such as copolymers of methyl vinyl ether and maleic anhydride (3) Acidic acrylic polymer compounds such as acrylic acid alkyl ester-methacrylic acid alkyl ester copolymers (4) Polyvinyl Polyvinylpyrolidone polymer compounds such as pyrrolidone and copolymers of vinylpyrrolidone and vinyl acetate (5) Acidic polyvinyl acetate polymer compounds such as copolymers of vinyl acetate and crotonic acid (6) Hydroxyethylcellulose Cationized cellulose (7) Natural polymer compounds such as chitin and chitosan
Among these polymer compounds, those having acid groups are preferably used after being neutralized with a suitable alkali agent. Further, these polymer compounds may be used alone or in combination of two or more.

上記した高分子化合物の配合量に特に限定はないが、組
成物全体の0.1〜10%(重量%、以下同様)とする
ことが好ましい。0.1%未満では毛髪のセット力が低
下することがあり、10%を超えると毛髪のごわつき、
べたつきが生じることがある。
Although there is no particular limitation on the amount of the above-mentioned polymer compound, it is preferably 0.1 to 10% (weight %, same hereinafter) of the entire composition. If it is less than 0.1%, the setting power of the hair may decrease, and if it exceeds 10%, the hair will become stiff.
Stickiness may occur.

本発明のヘアスプレー組成物は、上記成分に加え、下記
一般式(1) で示される分子内にアミド基を持つグアニジン誘導体や
それらの塩を含有する。
The hair spray composition of the present invention contains, in addition to the above-mentioned components, a guanidine derivative having an amide group in the molecule represented by the following general formula (1) or a salt thereof.

ここで、(1)式中の置換基R,は、炭素数1〜22、
好ましくは11〜19の分岐状又は直鎖状のアルキル基
又はアルケニル基であり、例えばC目Hzs    r
   CItHzs    、   ClJzt   
 、   Cl4H2IC+sHs+  、Cl6H3
3、ClJxs  、(CJ+t)zcH−4CzHs
C+sHx。−などの基が好適である。
Here, the substituent R in formula (1) has 1 to 22 carbon atoms,
Preferably it is a branched or straight-chain alkyl group or alkenyl group of 11 to 19, for example,
CItHzs, ClJzt
, Cl4H2IC+sHs+ , Cl6H3
3, ClJxs, (CJ+t)zcH-4CzHs
C+sHx. Groups such as - are suitable.

また、置換基Aは、炭素数1〜10、好ましくは2〜6
の分岐状又は直鎖状のアルキレン基又はアルケニレン基
であり、例えばメチレン基、エチレン基、プロピレン基
、ブチレン基、ペンチレン基、ヘキシレン基、イソプロ
ピレン基、2−ペンテニル基、2−エチルブチレン基な
どが挙げられ、mは1又は0である。
Further, substituent A has 1 to 10 carbon atoms, preferably 2 to 6 carbon atoms.
A branched or linear alkylene group or alkenylene group, such as a methylene group, ethylene group, propylene group, butylene group, pentylene group, hexylene group, isopropylene group, 2-pentenyl group, 2-ethylbutylene group, etc. m is 1 or 0.

なお、nは1〜5の整数である。Note that n is an integer of 1 to 5.

更に、(1)式のグアニジン誘導体は、通常、塩の形で
配合され、具体的には塩酸塩等の無機酸塩、グリコール
酸塩、酢酸塩、クエン酸塩、酸性アミノ酸塩等の有機酸
塩などとして用いることができるが、水への溶解性等の
点から無機酸塩とする場合は塩酸塩、有機酸塩とする場
合はグリコール酸塩が望ましい。
Furthermore, the guanidine derivative of formula (1) is usually formulated in the form of a salt, specifically inorganic acid salts such as hydrochloride, organic acids such as glycolate, acetate, citrate, and acidic amino acid salts. It can be used as a salt, but from the viewpoint of solubility in water, hydrochloride is preferable when using an inorganic acid salt, and glycolate is preferable when using an organic acid salt.

この場合、(1)式のグアニジン誘導体及びその塩は、
1種を単独で配合しても、2種以上を併用してもよく、
また、その配合量は別に制限されないが、全体の0.0
1〜5%、特に0.02〜3%とすることが望ましい。
In this case, the guanidine derivative of formula (1) and its salt are:
One type may be blended alone, or two or more types may be used in combination.
In addition, the blending amount is not particularly limited, but the total amount is 0.0
It is desirable to set it as 1-5%, especially 0.02-3%.

0.01%未満では帯電防止効果が不十分となる場合が
あり、5%を越えるとべたつきを生じるだけでなく、ム
セや金属容器の腐食を生じることがある。
If it is less than 0.01%, the antistatic effect may be insufficient, and if it exceeds 5%, it may not only cause stickiness but also cause clumps and corrosion of the metal container.

本発明のヘアスプレー組成物には噴射剤が用いられるが
、噴射剤としては、この種の組成物に通常使用されてい
るものが支障なく用いられ、例示すると、LPG、ハロ
ゲン化炭化水素、ジメチルエーテルなどが挙げられる。
A propellant is used in the hair spray composition of the present invention, and as the propellant, those normally used in this type of composition can be used without any problem, and examples thereof include LPG, halogenated hydrocarbon, dimethyl ether, etc. Examples include.

本発明の組成物には、上記成分に加え他の任意成分を本
発明の効果に影響のない範囲で配合してもよい。そのよ
うな任意成分としては、例えば流動パラフィン、ワセリ
ン、固形パラフィン、スクワラン、オレフィンオリゴマ
ーなどの炭化水素類、ミリスチン酸イソトリデシル、オ
クタン酸セチル等のエステル類、メチルポリシロキサン
等のシリコーン類、エチレングリコール、1.3−ブチ
レングリコール、プロピレングリコール、グリセリン、
ソルビトールなどの保湿剤、天然高分子物質−等の増粘
剤、乳化剤、その地番種の溶剤、殺菌剤、ビタミン、タ
ンパク質、ロジン、アミノ酸、生薬、香料等の小量成分
などがある。
In addition to the above-mentioned components, the composition of the present invention may contain other optional components within a range that does not affect the effects of the present invention. Such optional components include, for example, hydrocarbons such as liquid paraffin, vaseline, solid paraffin, squalane, and olefin oligomers, esters such as isotridecyl myristate and cetyl octoate, silicones such as methylpolysiloxane, ethylene glycol, 1.3-butylene glycol, propylene glycol, glycerin,
These include moisturizers such as sorbitol, thickeners such as natural polymer substances, emulsifiers, solvents of the same type, bactericides, small amounts of ingredients such as vitamins, proteins, rosin, amino acids, herbal medicines, and fragrances.

〔発明の効果〕〔Effect of the invention〕

本発明によれば、帯電防止効果に優れ、かつ、使用時に
ムセを生じることなく、金属容器腐食性の低い、セット
力の強いヘアスブに一組成物を提供することができる。
According to the present invention, a composition can be provided for a hair dye that has an excellent antistatic effect, does not cause stiffness during use, has low corrosion resistance to metal containers, and has a strong setting power.

以下、実施例及び比較例を示し、本発明を具体的に説明
するが、本発明は下記実施例に限定されるものではない
。なお、各側の説明に先立って各側で採用した試験法に
ついて説明する。
EXAMPLES Hereinafter, the present invention will be specifically explained with reference to Examples and Comparative Examples, but the present invention is not limited to the following Examples. Before explaining each side, we will explain the test methods adopted by each side.

會員餐器廠食判 45℃で3か月間保存後開缶し、腐食の状態を調べ、次
の判定基準に従って評価した。
After storage at 45°C for 3 months, the cans were opened, the state of corrosion was examined, and evaluation was made according to the following criteria.

○:腐食がほとんど認められない △:中程度の腐食が起きている ×二g食の程度が著しい ム  セ 3m3のボックス内に試料2gを噴霧した後、専門パネ
ラ−4名により官能で評価した。
○: Almost no corrosion observed △: Moderate corrosion occurring × Significant degree of 2g consumption After spraying 2g of the sample into a 3m3 box, sensory evaluation was performed by four expert panelists. .

○:ムセを生じない △:若干ムセを生じる ×:ムセを生じる 滞JJ柚F性 毛束(8,5g、  20c++)をポリエステル製の
櫛を用いて20秒間で10回指通しした後、ファラデー
ボックスに入れ、櫛通しにより毛束に生じた電気量を電
位計により測定する。帯電防止性は同一毛束に20c劇
の距離から1.5gの試料を噴霧処理した後と処理する
前との毛束の電気量から以下の式によって求めた。
○: Does not cause frizz △: Slightly fluffy Place the hair in a box and measure the amount of electricity generated in the hair bundle by combing it using an electrometer. The antistatic property was determined by the following formula from the amount of electricity in the hair bundle after and before treatment, when 1.5 g of a sample was sprayed onto the same hair bundle from a distance of 20 centimeters.

Ql : 処理前の電気量(クーロン)Q7 : 処理
後の電気量(クーロン)帯電防止性の評価は、次の基準
による。
Ql: Quantity of electricity (coulombs) before treatment Q7: Quantity of electricity (coulombs) after treatment Evaluation of antistatic properties is based on the following criteria.

90%以上  : ◎良い 70〜90% 二 〇やや良い 50〜70% : △普通 30〜50% : ×やや劣る 30%以下  :××劣る 〈実施例1〜6.比較例1〜3〉 第1表に示すヘアスプレー組成物を調製し、その性能を
評価した。結果を同表に示す。
90% or more: ◎ Good 70-90% 2 〇 Fairly good 50-70%: △ Fair 30-50%: × Slightly poor 30% or less: XX Poor <Examples 1-6. Comparative Examples 1 to 3> Hairspray compositions shown in Table 1 were prepared and their performance was evaluated. The results are shown in the same table.

〈実施例7〉 下記組成のヘアスプレーを調製し、 評価した。<Example 7> Prepare a hairspray with the following composition, evaluated.

その性能を *3 : レオガードG(ライオン社製)〈実施例8〉 下記組成のヘアスプレーを調製し、その性能を評価した
Performance *3: Leoguard G (manufactured by Lion Corporation) <Example 8> A hairspray having the following composition was prepared and its performance was evaluated.

カチオン化セルロース ミリスチン酸イソプロピル ポリエチレングリコール 香    料 精製水 エタノール PG フロン12 本3 計 金属容器腐食性 ム  セ 帯電防止性 0.3% 0.5 0.3 0、1 微量 30.0 残部 20.0 12.0 ポリメタクリル酸エステルの両性化物 ミリスチン酸イソトリデシル ロ  ジ  ン 香    料 無水エタノール PG ジメチルエー−ル ”2.0 0.1 0.1 微量 残部 32.0 B、 0 計                   i o o
、 。
Cationized cellulose myristate Isopropyl polyethylene glycol Flavor Purified water Ethanol PG Freon 12 bottles 3 Total metal container corrosive properties Antistatic properties 0.3% 0.5 0.3 0, 1 Trace amount 30.0 Balance 20.0 12 .0 Amphoterized polymethacrylate ester Isotridecyl rosin myristate Fragrance Anhydrous ethanol PG Dimethyl ale 2.0 0.1 0.1 Trace remainder 32.0 B, 0 Total i o o
, .

Claims (1)

【特許請求の範囲】 1、毛髪固定用高分子化合物を含有するヘアスプレー組
成物において、下記一般式(1)▲数式、化学式、表等
があります▼・・・・・・(1) (但し、式中R^1は炭素数1〜22の分岐状又は直鎖
状のアルキル基又はアルケニル基であり、Aは炭素数1
〜10の分岐状又は直鎖状のアルキレン基又はアルケニ
レン基であり、mは0又は1である。また、nは1〜5
の整数である。) で示される分子内にアミド基を持つグアニジン誘導体及
びそれらの塩から選ばれる1種又は2種以上を配合した
ことを特徴とするヘアスプレー組成物。
[Claims] 1. In a hair spray composition containing a hair fixing polymer compound, the following general formula (1) ▲ includes numerical formulas, chemical formulas, tables, etc. ▼ (1) (However, , in the formula, R^1 is a branched or straight-chain alkyl group or alkenyl group having 1 to 22 carbon atoms, and A is a carbon number 1
~10 branched or linear alkylene groups or alkenylene groups, and m is 0 or 1. Also, n is 1 to 5
is an integer. 1. A hairspray composition comprising one or more selected from the group consisting of guanidine derivatives having an amide group in the molecule represented by the following formula and salts thereof.
JP16111090A 1990-06-19 1990-06-19 Hair spray composition Pending JPH0454116A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP16111090A JPH0454116A (en) 1990-06-19 1990-06-19 Hair spray composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP16111090A JPH0454116A (en) 1990-06-19 1990-06-19 Hair spray composition

Publications (1)

Publication Number Publication Date
JPH0454116A true JPH0454116A (en) 1992-02-21

Family

ID=15728799

Family Applications (1)

Application Number Title Priority Date Filing Date
JP16111090A Pending JPH0454116A (en) 1990-06-19 1990-06-19 Hair spray composition

Country Status (1)

Country Link
JP (1) JPH0454116A (en)

Cited By (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2007314571A (en) * 2004-04-27 2007-12-06 L'oreal Sa Anhydrous cosmetic compositions comprising fatty acid esters, non-ionic polymers and petrolatum oil
US9986809B2 (en) 2013-06-28 2018-06-05 The Procter & Gamble Company Aerosol hairspray product comprising a spraying device
US10131488B2 (en) 2015-06-01 2018-11-20 The Procter And Gamble Company Aerosol hairspray product comprising a spraying device
US10426979B2 (en) 2011-09-15 2019-10-01 The Procter And Gamble Company Aerosol hairspray product for styling and/or shaping hair
WO2021257786A1 (en) 2020-06-18 2021-12-23 Nutrition & Biosciences USA 4, Inc. Cationic poly alpha-1,6-glucan ethers and compositions comprising same
WO2023287684A1 (en) 2021-07-13 2023-01-19 Nutrition & Biosciences USA 4, Inc. Cationic glucan ester derivatives
WO2023081341A1 (en) 2021-11-05 2023-05-11 Nutrition & Biosciences USA 4, Inc. Compositions comprising one cationic alpha- 1,6-glucan derivative and one alpha- 1,3-glucan
WO2023114942A1 (en) 2021-12-16 2023-06-22 Nutrition & Biosciences USA 4, Inc. Compositions comprising cationic alpha-glucan ethers in aqueous polar organic solvents
WO2024015769A1 (en) 2022-07-11 2024-01-18 Nutrition & Biosciences USA 4, Inc. Amphiphilic glucan ester derivatives
WO2024081773A1 (en) 2022-10-14 2024-04-18 Nutrition & Biosciences USA 4, Inc. Compositions comprising water, cationic alpha-1,6-glucan ether and organic solvent

Cited By (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2007314571A (en) * 2004-04-27 2007-12-06 L'oreal Sa Anhydrous cosmetic compositions comprising fatty acid esters, non-ionic polymers and petrolatum oil
US10426979B2 (en) 2011-09-15 2019-10-01 The Procter And Gamble Company Aerosol hairspray product for styling and/or shaping hair
US11311749B2 (en) 2011-09-15 2022-04-26 The Procter And Gamble Company Aerosol hairspray for styling and/or shaping hair
US9986809B2 (en) 2013-06-28 2018-06-05 The Procter & Gamble Company Aerosol hairspray product comprising a spraying device
US10131488B2 (en) 2015-06-01 2018-11-20 The Procter And Gamble Company Aerosol hairspray product comprising a spraying device
WO2021257786A1 (en) 2020-06-18 2021-12-23 Nutrition & Biosciences USA 4, Inc. Cationic poly alpha-1,6-glucan ethers and compositions comprising same
WO2023287684A1 (en) 2021-07-13 2023-01-19 Nutrition & Biosciences USA 4, Inc. Cationic glucan ester derivatives
WO2023081341A1 (en) 2021-11-05 2023-05-11 Nutrition & Biosciences USA 4, Inc. Compositions comprising one cationic alpha- 1,6-glucan derivative and one alpha- 1,3-glucan
WO2023081346A1 (en) 2021-11-05 2023-05-11 Nutrition & Biosciences USA 4, Inc. Glucan derivatives for microbial control
WO2023114942A1 (en) 2021-12-16 2023-06-22 Nutrition & Biosciences USA 4, Inc. Compositions comprising cationic alpha-glucan ethers in aqueous polar organic solvents
WO2024015769A1 (en) 2022-07-11 2024-01-18 Nutrition & Biosciences USA 4, Inc. Amphiphilic glucan ester derivatives
WO2024081773A1 (en) 2022-10-14 2024-04-18 Nutrition & Biosciences USA 4, Inc. Compositions comprising water, cationic alpha-1,6-glucan ether and organic solvent

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