JPS61225109A - Caramel-containing composition - Google Patents
Caramel-containing compositionInfo
- Publication number
- JPS61225109A JPS61225109A JP60066186A JP6618685A JPS61225109A JP S61225109 A JPS61225109 A JP S61225109A JP 60066186 A JP60066186 A JP 60066186A JP 6618685 A JP6618685 A JP 6618685A JP S61225109 A JPS61225109 A JP S61225109A
- Authority
- JP
- Japan
- Prior art keywords
- caramel
- cysteine
- cosmetic
- food
- 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
Links
Classifications
-
- 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
- A61K8/60—Sugars; Derivatives thereof
-
- 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
- A61K8/40—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
- A61K8/44—Aminocarboxylic acids or derivatives thereof, e.g. aminocarboxylic acids containing sulfur; Salts; Esters or N-acylated derivatives thereof
- A61K8/447—Aminocarboxylic acids or derivatives thereof, e.g. aminocarboxylic acids containing sulfur; Salts; Esters or N-acylated derivatives thereof containing sulfur
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q19/00—Preparations for care of the skin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
- A61K2800/40—Chemical, physico-chemical or functional or structural properties of particular ingredients
- A61K2800/52—Stabilizers
- A61K2800/524—Preservatives
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Birds (AREA)
- Epidemiology (AREA)
- Dermatology (AREA)
- Jellies, Jams, And Syrups (AREA)
- Medicinal Preparation (AREA)
- Cosmetics (AREA)
Abstract
Description
【発明の詳細な説明】
[産業上の利用分野]
本発明はシスティンとカラメルとを含有してなる、保存
安定性に優れた組成物に関し、化粧品、医薬品、食品あ
るいは染料等の分野に有用な上記組成物を提供すること
を目的とする。[Detailed Description of the Invention] [Industrial Application Field] The present invention relates to a composition containing cysteine and caramel, which has excellent storage stability, and which is useful in the fields of cosmetics, pharmaceuticals, foods, dyes, etc. It is an object of the present invention to provide the above composition.
[従来の技術]
カラメルはサッカロースが160℃で融けて飴状となり
200℃になって褐色に変わった非結晶質の物質であ
る。水に溶け、黄褐色〜茶褐色を示す。[Prior Art] Caramel is an amorphous substance in which saccharose melts at 160°C to become candy-like and turns brown at 200°C. It dissolves in water and exhibits a yellow-brown to brown color.
サッカロースは二II類の−っでスクロース、ショ糖と
も言われ、構造はα−D−グルコピラノシルーβ−D−
フルクトフラノシドであり、広く植物界に存在する、サ
トウダイコン、サトウキビ、サトウカエデ類などから工
業的に製造し甜菜糖などとも呼ぶ。Saccharose is a class II substance and is also called sucrose or sucrose, and its structure is α-D-glucopyranosyl-β-D-
It is a fructofuranoside and is industrially produced from sugar beet, sugar cane, sugar maple, etc., which exists widely in the plant kingdom, and is also called beet sugar.
サッカロースより得られたカラメルの構造はいまだ細部
までは確認されておらず、被容体の状態によりきわめて
複雑な反応を示す。原料別、製造別に並カラメル、グル
コースカラメル、砂糖カラメルに分類されている。The structure of caramel obtained from saccharose has not yet been confirmed in detail, and it exhibits extremely complex reactions depending on the conditions of the recipient. It is classified by raw material and production into regular caramel, glucose caramel, and sugar caramel.
[発明が解決しようとする問題点]
これらカラメルは耐光性が弱く、化粧品や医薬品、食品
に配合した場合に温度や光によって簡単に分解、褪色し
てしまうという欠点があった。[Problems to be Solved by the Invention] These caramels have low light resistance, and when incorporated into cosmetics, medicines, and foods, they have the disadvantage of being easily decomposed and discolored by temperature and light.
上述の欠点を補うための試みは幾つか成されている。例
えば、2.2’−4,4’−テトラハイドロオキシベン
ゾフェノン、2−ヒドロキシ−4−メトキシヘンシフエ
ノン硫酸塩、ウロカニン酸、2−エチルへキシル−p−
ジメチルアミノベンゾエート等のいわゆる紫外線吸収剤
を併用して温度及び光に対する安定性を保とうとする方
法が試みられているが、その効果は未だ満足できるもの
とはいいがたい。Several attempts have been made to compensate for the above-mentioned drawbacks. For example, 2,2'-4,4'-tetrahydroxybenzophenone, 2-hydroxy-4-methoxyhensiphenone sulfate, urocanic acid, 2-ethylhexyl-p-
Attempts have been made to maintain stability against temperature and light by using a so-called ultraviolet absorber such as dimethylaminobenzoate, but the effects are still far from satisfactory.
本発明者等は上記事情に鑑み、温度及び光に対する保存
安定性に優れ、しかも化粧品、医薬品あるいは食品等の
基剤に配合した場合にも上記安定性が満足されるカラメ
ル組成物を得るべく鋭意研究を重ねた結果、カラメルと
共にシスティンを併用して用いれば上記目的が達成され
ることを見い出し、本発明を完成するに至った。In view of the above circumstances, the present inventors have worked diligently to obtain a caramel composition that has excellent storage stability against temperature and light, and that also satisfies the above stability when incorporated into bases for cosmetics, pharmaceuticals, foods, etc. As a result of repeated research, the inventors have discovered that the above object can be achieved by using cysteine in combination with caramel, and have completed the present invention.
L問題点を解決するための手段]
すなわち、本発明は、システィンと、カラメルとを含有
することを特徴とする組成物である。Means for Solving Problem L] That is, the present invention is a composition characterized by containing cysteine and caramel.
本発明において」二記カラメルとシスティンとの量比は
重量で10=1〜1:100の比率であることが好まし
い。In the present invention, the weight ratio of caramel and cysteine is preferably 10=1 to 1:100.
本発明の組成物には上記必須構成成分の他、必要に応し
て、非イオン界面活性剤、アニオン界面活性剤、カチオ
ン界面活性剤、両性界面活性剤、油分、ワックス、紫外
線吸収剤、防腐剤、酸化防止剤、有機溶媒、薬剤、水溶
性高分子、粉末、色素、香料、水等、医薬品、化粧品あ
るいは食品等の分野で汎用される成分を添加することも
できる。In addition to the above-mentioned essential components, the composition of the present invention may optionally include nonionic surfactants, anionic surfactants, cationic surfactants, amphoteric surfactants, oils, waxes, ultraviolet absorbers, and preservatives. It is also possible to add ingredients commonly used in the fields of pharmaceuticals, cosmetics, foods, etc., such as agents, antioxidants, organic solvents, drugs, water-soluble polymers, powders, pigments, fragrances, and water.
[発明の効果]
次に実験例及び実施例によって本発明をさらに詳細に説
明する。[Effects of the Invention] Next, the present invention will be explained in further detail with reference to experimental examples and examples.
実験例1
下記処方の組成物を製造し、50’C暗所1力月保存品
及びキセノンランプ30時間(温度50′c)照射品の
色調をそれぞれに対応する0℃暗所保存品と比較した。Experimental Example 1 A composition with the following formulation was manufactured, and the color tone of the product stored in the dark at 50'C for one month and the product irradiated with a xenon lamp for 30 hours (temperature 50'C) was compared with the corresponding product stored in the dark at 0°C. did.
結果を表−1に示す。The results are shown in Table-1.
処方
精製水 残部エチルアルコ
ール 10カラメル
o、ooi添加剤
0.01(以下余白)
表−1
−(精製水で置換) X 15.2シス
テイン 01.I
L−アスバギン酸 X 10.9L−
アスコルビン酸 △ 7.30・・・・・
・・・・はとんど褪色していない。Prescription purified water, balance ethyl alcohol, 10 caramel
o, ooi additive
0.01 (blank below) Table 1 - (replaced with purified water) X 15.2 Cysteine 01. IL-Asbagic acid X 10.9L-
Ascorbic acid △ 7.30・・・・・・
...has not faded at all.
△・・・・・・・・・若干褪色している。△・・・・・・・・・Slightly faded.
×・・・・・・・・・褪色が目立つ。×・・・・・・Fading is noticeable.
(以下余白)
表−1の結果より明らかな通り、システィンの配合によ
って、カラメルの光に対する安定性は大幅に改良される
。(The following is a blank space) As is clear from the results in Table 1, the stability of caramel against light is significantly improved by adding cysteine.
U実施例] 以下、本発明の実施例を示す。U example] Examples of the present invention will be shown below.
これらは本発明をより詳しく説明するものであり、本発
明を限定するものではない。なお、配合量は重量%であ
る。These are intended to explain the invention in more detail and are not intended to limit it. In addition, the compounding amount is weight%.
〔実施例1〕 ヘアトリートメント
IPOR(30モル)ベヘニル エーテル4.02 グ
リセリルモノステアレート 6.03 イソプロ
ピルミリステート 5.04 オクチルドデカ
ノール 5.05 流動パラフィン(#7
0) 3.06 脱水ラノリン
3.07 ステアリン酸
5.08 メチルパラベン
o、i9 プロピルパラベン 0.1
1Oカラメル 0.111
ジプロピレングリコール 5.012
グリセリン 5.013 シス
ティン 0.0114 精製
水 残 部15 香!M
O,3(製法)
1〜10を70〜80℃、11〜14を70℃以上に加
熱し均一に熔解する。溶解したら1〜10を攪拌しなが
ら11〜14を加え攪拌乳化する。その後攪拌冷却し6
0〜55°Cの間に15を加え35°Cまで攪拌冷却す
る。[Example 1] Hair treatment IPOR (30 mol) Behenyl ether 4.02 Glyceryl monostearate 6.03 Isopropyl myristate 5.04 Octyldodecanol 5.05 Liquid paraffin (#7
0) 3.06 Dehydrated lanolin
3.07 Stearic acid
5.08 Methylparaben
o, i9 Propylparaben 0.1
1O caramel 0.111
Dipropylene glycol 5.012
Glycerin 5.013 Cystine 0.0114 Purified water Balance 15 Fragrance! M
O, 3 (Manufacturing method) Heat 1 to 10 to 70 to 80°C and 11 to 14 to 70°C or higher and melt them uniformly. Once dissolved, add 11 to 14 while stirring 1 to 10 and stir to emulsify. After that, stir and cool 6.
15 was added between 0 and 55°C, and the mixture was stirred and cooled to 35°C.
〔実施例2〕 軟膏
■ グリセリルモノステアレート 5.0(自己
乳化型)
2 ワセリン 10.03
流動パラフィン(#70) 10.04 シ
リコン(KF96) 、0.25 セ
タノール 2.06 メチルパラ
ベン 0.17 ブチルパラヘン
0.18 カラメル
0.59 プロピレングリコール
10.010 システィン
0.111 精製水 残
部(製法)
1〜Bを70〜80℃、9〜11を70℃以上に加熱し
均一に溶解する。溶解したら1〜Bを攪拌しながら9〜
11を加え攪拌乳化する。その後35℃まで攪拌冷却す
る。[Example 2] Ointment ■ Glyceryl monostearate 5.0 (self-emulsifying type) 2 Vaseline 10.03
Liquid paraffin (#70) 10.04 Silicon (KF96), 0.25 Setanol 2.06 Methylparaben 0.17 Butylparahen
0.18 caramel
0.59 Propylene glycol
10.010 Sistine
0.111 Purified water remainder
Part (Manufacturing method) Heat 1 to B to 70 to 80°C and 9 to 11 to 70°C or higher to uniformly dissolve. Once dissolved, mix 1~B while stirring 9~
Add 11 and stir to emulsify. Thereafter, the mixture is stirred and cooled to 35°C.
*2シコニソクスリキソドAB・・・−丸Wn K、に
、* :紫根エキスのアルミニウムキレート物をタンノ
マクと結合させたもの。*2 Shiconisoxulixod AB...-Maru Wn K, *: A product in which aluminum chelate of purple root extract is combined with Tannomaku.
〔実施例3〕 ヘアトニック
I POR(60モル)硬化ヒマシ油 5.02
エタノール 50.03 ビ
タミンHO91
4カラメル 0.0151−
メントール 0.16 香料
0.77 システィン
o、oot8 グリセリン
5.09 精製水
残 部(製法)
1〜6を40℃に加熱し均一に熔解する。均一に混合し
た7〜9を1〜6に加え攪拌混合する。[Example 3] Hair Tonic I POR (60 mol) Hydrogenated Castor Oil 5.02
Ethanol 50.03 Vitamin HO91 4 Caramel 0.0151-
Menthol 0.16 Fragrance 0.77 Cystine o, oot8 Glycerin
5.09 Purified water
Remainder (manufacturing method) Heat 1 to 6 to 40°C and melt uniformly. Add homogeneously mixed 7 to 9 to 1 to 6 and stir and mix.
〔実施例4〕 アフターシェーブローション1 エタノ
ール 552 ニスセーフ20
10 0.83 A S L−24
0,05
41−メントール 0,01
5 香料 0.36 カ
ラメル 0.057 アラン
トイン 0.058 クエン酸
0.059 クエン酸ソーダ
0.0610 グリセリン
2.Oll システィン
0.00512 精製水
残 部(製法)
1〜6を均一に混合溶解する。これを均一に混合溶解し
た7〜12を加え攪拌混合する。[Example 4] Aftershave lotion 1 Ethanol 552 Varnishsafe 20
10 0.83 ASL-24
0,05 41-menthol 0,01
5 Flavor 0.36 Caramel 0.057 Allantoin 0.058 Citric acid
0.059 Sodium citrate 0.0610 Glycerin
2. Oll Sistine
0.00512 Purified water
Remainder (manufacturing method) Mix and dissolve 1 to 6 uniformly. Add 7 to 12 which have been uniformly mixed and dissolved, and stir and mix.
〔実施例5〕 クリーム
I POB (15モル)植物油脂肪酸 1.
5エステル
2 ソルビタンセスキオレエート 3.53 イ
ソプロピルミリステート 10.04 流動パラ
フィン(#70)10.05 セタノール
4.06 パラフィンワックス
5.07 ミツロウ 1
0.08 メチルパラベン 0.1
9 ブチルパラベン 0.11Oカ
ラメル 1.011 ホウ
砂 0.5I2 プロピレ
ングリコール 2.013 システィン
0,0114 精製水
残 部15 香料
0.4(製法)
1〜IOを70〜80℃、11〜14を70℃以上に加
熱し均一に溶解する。熔解したら1〜10を攪拌しなが
ら11〜14を加え攪拌乳化する。その後攪拌冷却し6
0〜55℃の間に15を加え35℃まで攪拌冷却する。[Example 5] Cream I POB (15 mol) Vegetable oil fatty acid 1.
5 ester 2 Sorbitan sesquioleate 3.53 Isopropyl myristate 10.04 Liquid paraffin (#70) 10.05 Setanol
4.06 Paraffin wax
5.07 Beeswax 1
0.08 Methylparaben 0.1
9 Butylparaben 0.11O caramel 1.011 Borax 0.5I2 Propylene glycol 2.013 Cysteine
0,0114 Purified water
Remaining part 15 fragrance
0.4 (Production method) Heat 1 to IO to 70 to 80°C and 11 to 14 to 70°C or higher to uniformly dissolve them. Once melted, add 11 to 14 while stirring 1 to 10 and stir to emulsify. After that, stir and cool 6.
15 was added between 0 and 55°C, and the mixture was stirred and cooled to 35°C.
実施例2〜6により光及び温度安定性が良好な組成物を
得ることができた。In Examples 2 to 6, compositions with good light and temperature stability could be obtained.
Claims (1)
る組成物。(1) A composition characterized by containing cysteine and caramel.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP60066186A JPS61225109A (en) | 1985-03-29 | 1985-03-29 | Caramel-containing composition |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP60066186A JPS61225109A (en) | 1985-03-29 | 1985-03-29 | Caramel-containing composition |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS61225109A true JPS61225109A (en) | 1986-10-06 |
Family
ID=13308558
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP60066186A Pending JPS61225109A (en) | 1985-03-29 | 1985-03-29 | Caramel-containing composition |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS61225109A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE4124081A1 (en) * | 1990-07-20 | 1992-01-23 | Egyt Gyogyszervegyeszeti Gyar | 1 OR MORE LENS-SENSITIVE (N) AND, WHERE APPROPRIATE, IN WATER BAD LIQUID, SUBSTANCE (S), SUBSTANCES AND / OR OTHER ADDITIVE (S) AUXILIARY SUBSTANCE (S), AND SOLID PHARMACEUTICALS CONTAINING AT LEAST ONE IRRIGATING AGENT, AND SOLUTIONS OF SUCH SUBSTANCES ACTIVE INGREDIENTS |
JP2013139398A (en) * | 2011-12-28 | 2013-07-18 | Ikeda Shokken Kk | Enzyme inhibitor |
-
1985
- 1985-03-29 JP JP60066186A patent/JPS61225109A/en active Pending
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE4124081A1 (en) * | 1990-07-20 | 1992-01-23 | Egyt Gyogyszervegyeszeti Gyar | 1 OR MORE LENS-SENSITIVE (N) AND, WHERE APPROPRIATE, IN WATER BAD LIQUID, SUBSTANCE (S), SUBSTANCES AND / OR OTHER ADDITIVE (S) AUXILIARY SUBSTANCE (S), AND SOLID PHARMACEUTICALS CONTAINING AT LEAST ONE IRRIGATING AGENT, AND SOLUTIONS OF SUCH SUBSTANCES ACTIVE INGREDIENTS |
JP2013139398A (en) * | 2011-12-28 | 2013-07-18 | Ikeda Shokken Kk | Enzyme inhibitor |
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