JPS58110512A - Cosmetic composition - Google Patents

Cosmetic composition

Info

Publication number
JPS58110512A
JPS58110512A JP21536381A JP21536381A JPS58110512A JP S58110512 A JPS58110512 A JP S58110512A JP 21536381 A JP21536381 A JP 21536381A JP 21536381 A JP21536381 A JP 21536381A JP S58110512 A JPS58110512 A JP S58110512A
Authority
JP
Japan
Prior art keywords
cosmetic composition
compound
amino acid
acid
alkyl ester
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.)
Granted
Application number
JP21536381A
Other languages
Japanese (ja)
Other versions
JPH0340005B2 (en
Inventor
Hideo Kurokawa
黒川 秀雄
Isamu Nakashige
中重 勇
Nobuyuki Yamamoto
信之 山本
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 JP21536381A priority Critical patent/JPS58110512A/en
Publication of JPS58110512A publication Critical patent/JPS58110512A/en
Publication of JPH0340005B2 publication Critical patent/JPH0340005B2/ja
Granted legal-status Critical Current

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q5/00Preparations for care of the hair
    • A61Q5/12Preparations containing hair conditioners
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/33Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
    • A61K8/34Alcohols
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/40Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
    • A61K8/44Aminocarboxylic acids or derivatives thereof, e.g. aminocarboxylic acids containing sulfur; Salts; Esters or N-acylated derivatives thereof
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q19/00Preparations for care of the skin

Abstract

PURPOSE:The titled stable composition having an adjusted pH of a system of 1.5-6, properties mild to the skin, suppressing hydrolysis at high temperature, obtained by adding a compound having a specific inductive capacity to a cosmetic composition comprising an amino acid alkyl ester salt as a base. CONSTITUTION:A cosmetic composition comprising an amino acid alkyl ester salt as a base material is blended with 5.0-50.0wt% preferably 20.0-50.0wt% compound having a specific inductive capacity at 25 deg.C of 5.0-40.0, and adjusted to pH of 1.6-6. For example, an inorganic acid such as hydrochloric acid, sulfuric acid, and organic acid such as acetic acid, tartaric acid, etc. is used as the pH adjustor. Isopropyl alcohol, propylene glycol, 1,3-butylene glycol, etc. may be cited as the compound having a specific inductive capacity of 5.0-40.0. Glycinecetyl ester hydrochloride, etc. may be cited as the base material of the cosmetic composition.

Description

【発明の詳細な説明】 本発明は、アミノ酸アルキルエステル塩t−基材として
用いる低加水分解性の化粧品組成物に関する。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a low hydrolyzable cosmetic composition for use as an amino acid alkyl ester salt t-base.

アミノ酸と高級アルコールとから誘導されたアミノ酸ア
ル÷ルエステル塩は、近年、皮膚マイルド性を有する化
粧品基材としての有用性が広く昭められ多用されている
が、一方、アルカリ性において加水分解を生じ、そのた
め乳化安定性が劣化し、更には粘度の減少や相分離をも
生ずるなど、製品に対し悪影響を与えるという欠点があ
る。そのため、アミノ酸アルキルエ、ステル塩を化粧品
基材として用いる場合、一般に系の−を酸性に調節して
加水分解を抑えているが、しかし高温下では酸性にして
もアミノ酸アルキルエステル塩の加水分解は完全に抑え
られるとは言い難い。
Amino acid alcohol ester salts derived from amino acids and higher alcohols have been widely used in recent years due to their usefulness as skin-friendly cosmetic base materials. As a result, emulsion stability deteriorates, and furthermore, viscosity decreases and phase separation occurs, resulting in negative effects on the product. Therefore, when amino acid alkyl ester salts are used as cosmetic base materials, hydrolysis is generally suppressed by adjusting the - of the system to acidity. It is difficult to say that it can be suppressed.

一般に、アミノ酸アルキルエステル塩の加水分解速度の
程度を表わす酸−塩基触媒速度定数は、下記のように表
わされる。
Generally, the acid-base catalyst rate constant, which represents the degree of hydrolysis rate of an amino acid alkyl ester salt, is expressed as follows.

K、=(虻) (OH−) (ko:無触媒速度定数、kI:酸触媒速度定数、kO
H:アルカリ触媒速度定数) 一方、種々のエステルの酸及び塩基触媒定数は、下記の
表に示す値である。
K, = (fly) (OH-) (ko: non-catalytic rate constant, kI: acid catalyzed rate constant, kO
H: Alkaline catalyst rate constant) On the other hand, the acid and base catalyst constants of various esters are the values shown in the table below.

上記表から、どのエステルもkMよJ” ONの方が大
きく、即ちアルカリ側で加水分解が生ずることがわかる
。前述のように、一般に〆1を下げると加水分解率は下
がる傾向にあるが、40’Cや50℃の高温での加水分
解を十分に抑えることは困難である・ 本発明は、このような技術的課題に対してなされたもの
で、基材として含まれるアミノ酸アルキルエステル塩の
高温での加水分解を極力抑えた、安定な化粧品組成物を
提供することを目的とする。
From the table above, it can be seen that for all esters, kM is larger on the J''ON side, that is, hydrolysis occurs on the alkaline side.As mentioned above, generally speaking, as the limit 1 is lowered, the hydrolysis rate tends to decrease. It is difficult to sufficiently suppress hydrolysis at high temperatures of 40°C or 50°C. The present invention was made to address these technical problems, and it The purpose is to provide a stable cosmetic composition that minimizes hydrolysis at high temperatures.

本発明の化粧品組成物は、アミノ酸アルキルエステル塩
を基材として用いる化粧品組成物であって、25℃にお
ける比誘電率が5.0〜40.0の化合物を5.0〜5
0.0重量−含有し、かっ1.5〜6の−に調整されて
いることを特徴とする。
The cosmetic composition of the present invention is a cosmetic composition that uses an amino acid alkyl ester salt as a base material, and contains a compound having a dielectric constant of 5.0 to 40.0 at 25°C.
It is characterized in that it contains 0.0 weight and is adjusted to 1.5 to 6 weight.

本発明の化粧品組成物において基材として用いられるア
ミノ酸アルキルエステル媒としては、グリシンセチルエ
ステル塩酸塩、グリシンステアリルエステル塩酸塩、グ
リシンセトステアリ#!J?#塩s塩% /”りシンベ
ヘニルニスfル塩酸塩、グリシン硬化牛脂エステル塩酸
塩、アラニンセチルエステル塩酸塩、アラニンステアリ
ルエステル塩酸塩、アラニンベヘニルエステル塩酸塩、
アラニンセトステアリルエステル塩酸塩、ノ々リンセチ
ルエステル硫酸塩、z49ンステアリルエステル硫酸塩
、パリンセトステア替k :t、 スfル硫酸塩、バリ
ンベヘニルエステル硫酸塩、ロイシンセチルエステル塩
酸塩、ロイシンステ7リルエステル塩酸塩、ロイシンセ
トステアリルエステル塩Wt塩、ロイシンベヘニルエス
テル塩酸塩、グルタンン酸ジセチルエステル塩酸塩、グ
ルタミン酸ゾステアリルエステル塙酸塩、グルタミン酸
ジセトステアリルエステル塩酸塩、グルタミン酸ジベヘ
ニルエステル塩酸塩、グリシンベタインセチルエステル
硫酸塩、グリシンベタインステアリルエステル塩酸塩、
グリシンベタインベヘニル硫酸塩等が挙げられるO また、系の−を1.5〜6の酸性にするためのpi(調
節剤としては、例えば、塩酸、硫酸等の無機酸、または
酢酸、酒石酸、クエン酸、P−)ルエンスルホン酸、脂
肪酸等の有機酸が用いられる。
Examples of the amino acid alkyl ester medium used as a base material in the cosmetic composition of the present invention include glycine cetyl ester hydrochloride, glycine stearyl ester hydrochloride, glycine cetyl ester hydrochloride, and glycine cetyl ester #! J? #Salt s Salt % /” Lysine behenyl ester hydrochloride, glycine hardened beef tallow ester hydrochloride, alanine cetyl ester hydrochloride, alanine stearyl ester hydrochloride, alanine behenyl ester hydrochloride,
Alanine cetostearyl ester hydrochloride, nonorin cetyl ester sulfate, z49n stearyl ester sulfate, palincetostearyl sulfate, sulfur sulfate, valine behenyl ester sulfate, leucine cetyl ester hydrochloride, leucine stearyl 7 Lyle ester hydrochloride, leucine setostearyl ester salt Wt salt, leucine behenyl ester hydrochloride, glutanic acid dicetyl ester hydrochloride, glutamic acid distearyl ester sulfate, glutamic acid dicetostearyl ester hydrochloride, glutamic acid dibehenyl ester hydrochloride, glycine Betaine cetyl ester sulfate, glycine betaine stearyl ester hydrochloride,
Glycine betaine behenyl sulfate, etc. are also mentioned. Organic acids such as P-)luenesulfonic acid and fatty acids are used.

25℃における比誘電率が′5.0〜40.0の化合物
としては、イソプロピルアルコール(比誘電率18.3
 )、グロビレングリフール(32)、1.3−ブチレ
ングリコール(31)、エタノール(24,3)、メタ
ノール(32,6)等があり、特K、25℃における比
誘電率が20.0〜40.0の化合物が好ましい。25
℃における比誘電率が5.0未満の化合物では、アミノ
酸アルキルエステル塩の加水分解を抑制する効果が全く
なく、また40.0を越える化合物でも、加水分解抑制
効果は小さい。
As a compound having a relative permittivity of 5.0 to 40.0 at 25°C, isopropyl alcohol (relative permittivity 18.3
), globylene glycol (32), 1,3-butylene glycol (31), ethanol (24,3), methanol (32,6), etc., and have a special dielectric constant of 20.0 at 25°C. ~40.0 compounds are preferred. 25
Compounds with a dielectric constant of less than 5.0 at °C have no effect of inhibiting hydrolysis of amino acid alkyl ester salts, and even compounds with a dielectric constant of more than 40.0 have a small hydrolysis inhibiting effect.

25℃における比誘電率が5.0〜40.0の化合物の
配合量は、化粧品組成物全量に対し5.0〜50.0重
量−であるが、特に好ましい量は20.0〜50.0重
量−である。この配合量が5、0重量−未満では、高温
でのアミノ酸アルキルエステル塩の加水分解抑制作用は
殆んどみられず、SO,O重量%を越えると、加水分解
抑制効果はほぼ一定となるが、化粧品組成物の粘度が異
常に高くなり、例えば皮膚用クリームに適用した場合、
皮膚へののびが悪くなって、処方上好ましくない。
The compounding amount of the compound having a dielectric constant of 5.0 to 40.0 at 25°C is 5.0 to 50.0% by weight based on the total amount of the cosmetic composition, and a particularly preferable amount is 20.0 to 50.0% by weight. 0 weight. When this amount is less than 5.0% by weight, the hydrolysis inhibitory effect of the amino acid alkyl ester salt at high temperatures is hardly observed, and when it exceeds SO,O weight%, the hydrolysis inhibitory effect remains almost constant. However, when the viscosity of the cosmetic composition becomes abnormally high, for example when applied to a skin cream,
It spreads poorly onto the skin, making it undesirable in terms of prescription.

なお、本発明の化粧品組成物においては、25℃におけ
る比誘電率が5.0〜40.0の化合物を単に配合した
だけでは、基材として用いられているアミノ酸アルキル
エステル塩の加水分解を抑制する効果は発揮されず、七
のような特定の比誘電率を有する化合物の配合と、系の
−を1.5〜6に調整することの両方の条件を温良して
初めて本発明の効果である高温でのアミン酸アルキルエ
ステル塩の加水分解を抑制することができる。
In addition, in the cosmetic composition of the present invention, simply adding a compound having a dielectric constant of 5.0 to 40.0 at 25°C will not suppress the hydrolysis of the amino acid alkyl ester salt used as the base material. However, the effect of the present invention was not achieved until both the conditions of blending a compound with a specific dielectric constant such as 7 and adjusting the - of the system to 1.5 to 6 were satisfied. It is possible to suppress the hydrolysis of the amine acid alkyl ester salt at a certain high temperature.

本発明の化粧品組成物は、上述の皮膚用化粧料K 限う
−r 、ヘアコンrイシ冒ナー、ヘアリンス、ヘアクリ
ーム等の毛髪化粧料の用途に適用することが可能である
The cosmetic composition of the present invention can be applied to hair cosmetics such as the above-mentioned skin cosmetics, hair conditioners, hair rinses, and hair creams.

次に、本発明の実施4例と比較例を示し、本発明の効果
をより具体的に説明する。なお、各側の説明に外立って
、各側で採用した試験法について説明する。
Next, four examples of the present invention and a comparative example will be shown, and the effects of the present invention will be explained in more detail. In addition to the explanations provided by each side, the test methods adopted by each side will be explained below.

試験法(加水分解率) 化粧品組成物試料を50℃の恒温槽内で1ケ月保存した
後、基材として含まれるアミノ酸アルキルエステル塩の
加水分解率を測定し九〇加水分解率の評価は、下記の3
段階の評価基準による。
Test method (hydrolysis rate) After storing the cosmetic composition sample in a constant temperature bath at 50°C for one month, the hydrolysis rate of the amino acid alkyl ester salt contained as a base material was measured. 3 below
Based on stage evaluation criteria.

評価基準 ◎:加水分解率  90〜5チ Q:   #     5〜15チ X:   #     15チ以上 試験例1 下記@−1Fc示す配合組成の5種の毛髪化粧料を調製
し、それらの化粧料中に含まれるアミノ酸アルキルエス
テル塩の加水分解率を試験した。その結果を同表に示す
。同表から明らかなように、25℃で32の比誘電率を
有する化合物テするグロピレングリコールを5〜50−
の範囲で含む場合、加水分解率はθ〜51Gに抑えるこ
とが出来た。
Evaluation criteria ◎: Hydrolysis rate 90-5chi Q: #5-15chi The hydrolysis rate of amino acid alkyl ester salts contained in The results are shown in the same table. As is clear from the same table, glopylene glycol, which is a compound having a dielectric constant of 32 at 25°C,
When it was included in the range of , the hydrolysis rate could be suppressed to θ~51G.

表  −1 *1 比誘電率32(25℃)、*2PH:2試験例2 下記表−2に示す配合組成の6種の毛髪化粧料を調製し
、それらの化粧料中に含まれるアミノ酸アルキルエステ
ル塩の加水分解率を試験した。その結果を同表に示す。
Table-1 *1 Relative dielectric constant 32 (25°C), *2 PH: 2 Test Example 2 Six types of hair cosmetics having the formulation shown in Table-2 below were prepared, and the alkyl amino acids contained in these cosmetics were evaluated. The hydrolysis rate of the ester salt was tested. The results are shown in the same table.

同表から明らかなヨウニ、グロピレングリコールが5〜
50eIk配合されていても、−が6を越える値では加
水分解を抑えることができず、−を1.5〜6に調整し
て初めて加水分解率をO〜55Gに抑えられることがわ
かる。
From the same table, it is clear that chlorophyllene glycol and glopylene glycol are 5 to 5.
It can be seen that even if 50eIk is blended, hydrolysis cannot be suppressed when - is greater than 6, and the hydrolysis rate can be suppressed to 0 to 55G only by adjusting - to 1.5 to 6.

試験例3 種々の比誘電率の化合物を含む下記表−3に示す配合組
成の8種の化粧料組成物を調製し、それらの化粧料中に
含まれるアミノ酸アルキルエステル塩の加水分解率を試
験した。その結果を同表に示す。同表から明らかなよう
に、25℃での比誘電率が5.0〜40.0の化合物を
5.0〜50.0重量%配合したときに、加水分解率を
抑制するととが出来る。
Test Example 3 Eight types of cosmetic compositions containing compounds with various dielectric constants and having the formulation shown in Table 3 below were prepared, and the hydrolysis rate of amino acid alkyl ester salts contained in these cosmetics was tested. did. The results are shown in the same table. As is clear from the same table, the hydrolysis rate can be suppressed when 5.0 to 50.0% by weight of a compound having a dielectric constant of 5.0 to 40.0 at 25° C. is blended.

表  −3 試験例 5.0〜40.Oの比誘電率(25℃)を有する化合物
を含む、アミノ酸アルキルエステル塩ヲ基材とするクリ
ームを調製し、アミノ酸アルキルエステル塩の加水分解
率を試験した。このクリームは、高温下で4加水分解が
抑制された優れた化粧料である。
Table-3 Test examples 5.0 to 40. A cream based on an amino acid alkyl ester salt containing a compound having a dielectric constant of O (25° C.) was prepared and the hydrolysis rate of the amino acid alkyl ester salt was tested. This cream is an excellent cosmetic material with suppressed 4-hydrolysis at high temperatures.

表  −4 −7;Table-4 -7;

Claims (1)

【特許請求の範囲】[Claims] アミノ酸アルキルエステル塩を基材として用いる化粧品
組成物であって、25℃における比誘電率が5.0〜4
0,0の化合物を5.0〜50.0重量%含有し、かつ
1.5〜6の−に調整された化粧品組成物。
A cosmetic composition using an amino acid alkyl ester salt as a base material, which has a dielectric constant of 5.0 to 4 at 25°C.
A cosmetic composition containing 5.0 to 50.0% by weight of a 0.0 compound and adjusted to -1.5 to 6.
JP21536381A 1981-12-24 1981-12-24 Cosmetic composition Granted JPS58110512A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP21536381A JPS58110512A (en) 1981-12-24 1981-12-24 Cosmetic composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP21536381A JPS58110512A (en) 1981-12-24 1981-12-24 Cosmetic composition

Publications (2)

Publication Number Publication Date
JPS58110512A true JPS58110512A (en) 1983-07-01
JPH0340005B2 JPH0340005B2 (en) 1991-06-17

Family

ID=16671048

Family Applications (1)

Application Number Title Priority Date Filing Date
JP21536381A Granted JPS58110512A (en) 1981-12-24 1981-12-24 Cosmetic composition

Country Status (1)

Country Link
JP (1) JPS58110512A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS617206A (en) * 1984-06-21 1986-01-13 Lion Corp Cell activator
FR2983403A1 (en) * 2011-12-05 2013-06-07 Oreal Composition in emulsion form, useful for cosmetic treatment of keratin materials, comprises phospholipid and cationic emulsifier of neutral amino acid esters whose amine function is partially or totally neutralized, and fatty alcohol
US8690650B2 (en) 2009-07-21 2014-04-08 Hyundai Motor Company Air-conditioner for vehicle

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5022096A (en) * 1973-06-26 1975-03-08
JPS5523241A (en) * 1978-08-05 1980-02-19 Kunijiro Matsushita Coupling process for continuous underground wall by use of precast concrete member
JPS5857309A (en) * 1981-10-01 1983-04-05 Lion Corp Hair cosmetic
JPS5892607A (en) * 1981-11-26 1983-06-02 Lion Corp Hair cosmetic

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5022096A (en) * 1973-06-26 1975-03-08
JPS5523241A (en) * 1978-08-05 1980-02-19 Kunijiro Matsushita Coupling process for continuous underground wall by use of precast concrete member
JPS5857309A (en) * 1981-10-01 1983-04-05 Lion Corp Hair cosmetic
JPS5892607A (en) * 1981-11-26 1983-06-02 Lion Corp Hair cosmetic

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS617206A (en) * 1984-06-21 1986-01-13 Lion Corp Cell activator
US8690650B2 (en) 2009-07-21 2014-04-08 Hyundai Motor Company Air-conditioner for vehicle
FR2983403A1 (en) * 2011-12-05 2013-06-07 Oreal Composition in emulsion form, useful for cosmetic treatment of keratin materials, comprises phospholipid and cationic emulsifier of neutral amino acid esters whose amine function is partially or totally neutralized, and fatty alcohol

Also Published As

Publication number Publication date
JPH0340005B2 (en) 1991-06-17

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