JPS5864128A - Alcohol-containing aqueous gel composition - Google Patents
Alcohol-containing aqueous gel compositionInfo
- Publication number
- JPS5864128A JPS5864128A JP56164451A JP16445181A JPS5864128A JP S5864128 A JPS5864128 A JP S5864128A JP 56164451 A JP56164451 A JP 56164451A JP 16445181 A JP16445181 A JP 16445181A JP S5864128 A JPS5864128 A JP S5864128A
- Authority
- JP
- Japan
- Prior art keywords
- alcohol
- gel
- polyglycerin
- gel composition
- isostearate
- 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
Links
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 title claims abstract description 28
- 239000000203 mixture Substances 0.000 title claims abstract description 24
- XDOFQFKRPWOURC-UHFFFAOYSA-N 16-methylheptadecanoic acid Chemical compound CC(C)CCCCCCCCCCCCCCC(O)=O XDOFQFKRPWOURC-UHFFFAOYSA-N 0.000 claims abstract description 28
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 10
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims abstract description 6
- 235000011187 glycerol Nutrition 0.000 claims abstract description 3
- 239000000499 gel Substances 0.000 claims description 31
- 150000001875 compounds Chemical class 0.000 claims description 12
- 229920000223 polyglycerol Polymers 0.000 claims description 11
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 8
- -1 ether phosphates Chemical class 0.000 claims description 8
- 239000000017 hydrogel Substances 0.000 claims description 6
- 229920006317 cationic polymer Polymers 0.000 claims description 4
- 241001465754 Metazoa Species 0.000 claims description 3
- 229910019142 PO4 Inorganic materials 0.000 claims description 3
- 239000010775 animal oil Substances 0.000 claims description 3
- 229940057995 liquid paraffin Drugs 0.000 claims description 3
- 235000021317 phosphate Nutrition 0.000 claims description 3
- 229920002545 silicone oil Polymers 0.000 claims description 3
- 235000015112 vegetable and seed oil Nutrition 0.000 claims description 3
- 239000008158 vegetable oil Substances 0.000 claims description 3
- 239000001993 wax Substances 0.000 claims description 3
- 239000003349 gelling agent Substances 0.000 abstract description 5
- 239000002537 cosmetic Substances 0.000 abstract description 4
- 239000006071 cream Substances 0.000 abstract description 3
- 239000006210 lotion Substances 0.000 abstract description 3
- 239000000825 pharmaceutical preparation Substances 0.000 abstract description 2
- 229940127557 pharmaceutical product Drugs 0.000 abstract description 2
- 231100000252 nontoxic Toxicity 0.000 abstract 2
- 230000003000 nontoxic effect Effects 0.000 abstract 2
- 239000000178 monomer Substances 0.000 abstract 1
- 235000019441 ethanol Nutrition 0.000 description 21
- 230000015572 biosynthetic process Effects 0.000 description 12
- 238000003786 synthesis reaction Methods 0.000 description 9
- 229920000642 polymer Polymers 0.000 description 8
- 150000002148 esters Chemical class 0.000 description 7
- WMFOQBRAJBCJND-UHFFFAOYSA-M Lithium hydroxide Chemical compound [Li+].[OH-] WMFOQBRAJBCJND-UHFFFAOYSA-M 0.000 description 6
- 235000014113 dietary fatty acids Nutrition 0.000 description 5
- 239000000194 fatty acid Substances 0.000 description 5
- 229930195729 fatty acid Natural products 0.000 description 5
- 239000002253 acid Substances 0.000 description 4
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 125000000962 organic group Chemical group 0.000 description 3
- 230000009974 thixotropic effect Effects 0.000 description 3
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 2
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 2
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 2
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- 241000287828 Gallus gallus Species 0.000 description 2
- 239000005642 Oleic acid Substances 0.000 description 2
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 2
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 2
- 150000004665 fatty acids Chemical class 0.000 description 2
- 235000013373 food additive Nutrition 0.000 description 2
- 239000002778 food additive Substances 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 2
- 230000007246 mechanism Effects 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 239000000693 micelle Substances 0.000 description 2
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 2
- 230000000704 physical effect Effects 0.000 description 2
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L sodium carbonate Substances [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- PRAKJMSDJKAYCZ-UHFFFAOYSA-N squalane Chemical compound CC(C)CCCC(C)CCCC(C)CCCCC(C)CCCC(C)CCCC(C)C PRAKJMSDJKAYCZ-UHFFFAOYSA-N 0.000 description 2
- 239000004094 surface-active agent Substances 0.000 description 2
- UZFMOKQJFYMBGY-UHFFFAOYSA-N 4-hydroxy-TEMPO Chemical compound CC1(C)CC(O)CC(C)(C)N1[O] UZFMOKQJFYMBGY-UHFFFAOYSA-N 0.000 description 1
- 229920001817 Agar Polymers 0.000 description 1
- 239000005639 Lauric acid Substances 0.000 description 1
- 239000004902 Softening Agent Substances 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 150000003934 aromatic aldehydes Chemical class 0.000 description 1
- 239000010495 camellia oil Substances 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000004020 conductor Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 229940105990 diglycerin Drugs 0.000 description 1
- GPLRAVKSCUXZTP-UHFFFAOYSA-N diglycerol Chemical compound OCC(O)COCC(O)CO GPLRAVKSCUXZTP-UHFFFAOYSA-N 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- IDGUHHHQCWSQLU-UHFFFAOYSA-N ethanol;hydrate Chemical compound O.CCO IDGUHHHQCWSQLU-UHFFFAOYSA-N 0.000 description 1
- 125000001033 ether group Chemical group 0.000 description 1
- 238000001879 gelation Methods 0.000 description 1
- 229940074774 glycyrrhizinate Drugs 0.000 description 1
- LPLVUJXQOOQHMX-QWBHMCJMSA-N glycyrrhizinic acid Chemical compound O([C@@H]1[C@@H](O)[C@H](O)[C@H](O[C@@H]1O[C@@H]1C([C@H]2[C@]([C@@H]3[C@@]([C@@]4(CC[C@@]5(C)CC[C@@](C)(C[C@H]5C4=CC3=O)C(O)=O)C)(C)CC2)(C)CC1)(C)C)C(O)=O)[C@@H]1O[C@H](C(O)=O)[C@@H](O)[C@H](O)[C@H]1O LPLVUJXQOOQHMX-QWBHMCJMSA-N 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 239000011261 inert gas Substances 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 239000000077 insect repellent Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- JXTPJDDICSTXJX-UHFFFAOYSA-N n-Triacontane Natural products CCCCCCCCCCCCCCCCCCCCCCCCCCCCCC JXTPJDDICSTXJX-UHFFFAOYSA-N 0.000 description 1
- 229920005615 natural polymer Polymers 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- 239000002674 ointment Substances 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 238000001935 peptisation Methods 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 238000007127 saponification reaction Methods 0.000 description 1
- 239000002453 shampoo Substances 0.000 description 1
- 239000010686 shark liver oil Substances 0.000 description 1
- 229940069764 shark liver oil Drugs 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 229940032094 squalane Drugs 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- 229920001059 synthetic polymer Polymers 0.000 description 1
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
- A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
- A61K8/39—Derivatives containing from 2 to 10 oxyalkylene groups
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/02—Cosmetics or similar toiletry preparations characterised by special physical form
- A61K8/04—Dispersions; Emulsions
- A61K8/042—Gels
-
- 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
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Epidemiology (AREA)
- Birds (AREA)
- Dispersion Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Emergency Medicine (AREA)
- Dermatology (AREA)
- Colloid Chemistry (AREA)
- Confectionery (AREA)
- Medicinal Preparation (AREA)
- Cosmetics (AREA)
Abstract
Description
【発明の詳細な説明】
本発明はアルコール含水ゲル組成物特にゲル化剤として
ポリグリセリンイソステアリン酸エステルを用いたゲル
化組成物に関するものであるO化粧品、医薬品等の分野
では、有機又は無機化合物を用いた種々のゲル化組成物
が使用されている0この用途に供する有機化合物として
は天然高分子やその誘導体中合成高分子化合物をはじめ
芳香族アルデヒド多価アルコール誘導体や界面活性剤、
脂肪酸アマイド、金属石鹸等各種の化合物がその目的に
合わせて使用されている。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to an alcohol-containing hydrogel composition, particularly a gelling composition using polyglycerol isostearate as a gelling agent. Various gelling compositions have been used. Organic compounds used for this purpose include natural polymers and their derivatives, synthetic polymers, aromatic aldehydes, polyhydric alcohol derivatives, surfactants,
Various compounds such as fatty acid amides and metal soaps are used depending on the purpose.
化粧品や医薬品の場合には安全性が強調されるのは当然
であるが、ゲル状組成物を手に取シ使用する場合、寒天
ゲルの様な硬いゲルでは使用し難いので適当な粘度を有
する高粘度ゲル又は中面状ゲルで透明感を有し、使用し
た時にぬめシ感のない事が望まれていた。It is natural that safety is emphasized in the case of cosmetics and pharmaceuticals, but when using gel-like compositions, it is difficult to use hard gels such as agar gel, so it is necessary to have an appropriate viscosity. It was desired that the gel be a highly viscous gel or a medium gel that has a transparent feel and does not have a slimy feeling when used.
従来のゲル化剤では高分子化合物を用いたゲル化組成物
ではぬめシ感が残り、好ましくなく、一般的に界面活性
剤をペースとしたゲル組成物が。With conventional gelling agents, gelling compositions using polymer compounds leave a slimy feeling, which is undesirable, and gel compositions based on surfactants are generally used.
この用途に供されていた。例えば、ポリエチレンオキシ
ド高級アルコールエーテルや脂肪酸エステルやM肪酸ジ
ェタノールアミドを用いる方法中グリチルリチン酸塩等
を用いる方法があシー有効であるO
しかし、ゲル組成物の用途によっては比較的高い濃度の
アルコールを含有した含水ゲル組成物の形に調合する必
要のある場合には、高アルコール含量の領域では解膠現
象があ夛、ゲルが形成されない傾向があうた。アルコー
ル含水ゲルの形成ではアミンの窮導体たるボロキサミ′
ン(Polexamln・)[例えばBASF社Pol
ozamlne ]を用いる場合でもアルコールはに一
以下にする事が望ましいとされている。It was used for this purpose. For example, among methods using polyethylene oxide higher alcohol ethers, fatty acid esters, and M fatty acid jetanolamide, methods using glycyrrhizinate, etc. are effective. However, depending on the use of the gel composition, a relatively high concentration of alcohol When it is necessary to formulate a hydrogel composition containing , peptization occurs frequently in the region of high alcohol content, and a gel tends not to form. In the formation of alcohol-containing gels, boroxamines are essential conductors for amines.
(Polexamln) [for example, BASF Polex
Even when using [Ozamlne], it is said that it is desirable to keep the alcohol content to 1:1 or less.
水溶液系でのゲルの形成機構は種々提案されているが、
工・−チル結合を含む化合物の場合には。Various mechanisms of gel formation in aqueous systems have been proposed;
In the case of compounds containing an -thyl bond.
水のプロトンが配位したエーテル型化合物の濃度が、臨
界ミセル濃度に達してマセルを形成し、ミセル中の水分
子は水素結合で固定されてゲルを形成すると考えられて
いるのでエーテル化合物のエーテル基の数やそれに結合
している有機基の数及び形で著しく物性が支配される。It is thought that the concentration of ether-type compounds to which water protons are coordinated reaches the critical micelle concentration to form macelle, and the water molecules in the micelles are fixed by hydrogen bonds to form a gel. The physical properties are significantly controlled by the number of groups and the number and shape of the organic groups bonded thereto.
従うてエーテル結合含有化合物の構造とそれに結合する
有機基の数、形、構造等で水分子の配位性並びに建セル
形成性が支配されるので物性等にゲル形成性は著しく変
化する事が想定される。Therefore, the structure of the ether bond-containing compound and the number, shape, structure, etc. of the organic groups bonded to it govern the coordination of water molecules and the cell-forming property, so the gel-forming property may change significantly in terms of physical properties, etc. is assumed.
食品添加剤としても広く検討されて来ているポリグリセ
リンの場合、一般的に知られているステアリン酸、オレ
イン酸、ノ2ル?テン酸、ラウリン酸等の脂肪酸エステ
ルは乳化剤としては有効であるが1本願の目的のゲル化
特性は期待出来ない〇又、一般的に知られているイソス
テアリン酸エステルも同様な用途に適用される事が知ら
れているが、同様にゲル化特性を有する事は知られてい
なかった0
本発明者らは従来よシこれら各種の脂肪酸エステルの合
成と利用の研究を行なってきたがその一環としてアルコ
ール含水ゲル組成物、特に咥チ又はそれ以上の濃度のア
ルコールを含む水性ゲル組成物の調製への利用について
研究しか結果、各種のHtFFIIエステルの中、ポリ
グリセリンインステアリン酸エステルがゲル化特性を有
し、前記ゲル組成物に有効に用いうろことが見出された
のであるO
かくて本発明はポリグリセリンイソステアリン酸エステ
ルと水及び低級アルコールを含むアルコール含水ゲル組
成物を提供するものである。In the case of polyglycerin, which has been widely considered as a food additive, the commonly known ingredients stearic acid, oleic acid, and oleic acid are commonly used. Fatty acid esters such as thenic acid and lauric acid are effective as emulsifiers, but cannot be expected to have the gelling properties that are the objective of this application.In addition, commonly known isostearate esters can also be used for similar purposes. However, it was not known that they also had gelling properties.The present inventors have been conducting research on the synthesis and utilization of these various fatty acid esters, and as part of this research, Research on its use in the preparation of alcohol-containing hydrogel compositions, particularly aqueous gel compositions containing alcohol at concentrations of mouth or higher, has shown that among the various HtFFII esters, polyglycerol instearate has the best gelling properties. Therefore, the present invention provides an alcohol-containing gel composition containing polyglycerol isostearate, water, and a lower alcohol.
本発明では前記ポリグリセリンイノステアリン酸エステ
ルとしては!〜を量体のグリセリンからなるポリグリセ
リンに対してモル比/−Jのイソステアリン酸を反応さ
せて見られた化合物が他のエステルと異なシ高アルコー
ル水溶液や高アルコール含水組成物をよくゲル化させる
性質を有するものとして%に好んで用いられる。In the present invention, the polyglycerol inostearate is! A compound found by reacting isostearic acid at a molar ratio of /-J with polyglycerin consisting of glycerin having a mass of ~ is different from other esters, and it gels well in high alcohol aqueous solutions and high alcohol water-containing compositions. It is preferable to use % as a property.
同じ量種のポリグリセリンでも3モル以上のイソステア
リン酸を反応させたエステルやBxJ〜参程度のポリグ
リセリン或いはジグリセリンに7〜3モルのイソステア
リン酸を反応させて得たエステルには同様なゲル化性は
認められない0この本願のエステルの持つ特異なゲル化
性発現や機序は明確でないがエーテル基の数ど残留する
水酸基の数及び結合゛している有機基の骨格構造と数の
バランスが良い為と想定している。Even with the same amount of polyglycerin, esters obtained by reacting 3 moles or more of isostearic acid, and esters obtained by reacting 7 to 3 moles of isostearic acid with polyglycerin or diglycerin of BxJ to BxJ, have similar gelation. Although the expression and mechanism of the unique gelling property of the ester of this application are not clear, it is important to understand the balance between the number of ether groups, the number of residual hydroxyl groups, and the skeletal structure and number of bonded organic groups. I assume this is because it is good.
1〜3モルのイソステアリン酸を!〜を量体のポリグリ
セリンに反応させる場合には1通常の方法例えば、水酸
化カリウム、水酸化ナトリウムや炭酸ナトリウム等の塩
基性触媒を用いて不活性ガス中でl!O−コ30″CK
加熱して容J+に合成する事が出来る。生成物は淡黄色
の粘稠液体であシ、イソステアリン酸のモル比により、
ゲルの性質が変fi、/−2’E、ルの場合には柔ゲル
となシ、λ〜3モルのエステルは硬ゲルを与える傾向が
ある〇ゲルの形成作業はアルコール又はアルコール含水
組成物ioo部に対し、、2j〜yo%又はそれ以上の
イソステア1フン酸エステルを加見て侵〜−℃に加温し
て溶解させた後、冷却して所期のゲルを得る事が出来る
。1 to 3 moles of isostearic acid! When ~ is reacted with a polymer of polyglycerin, a conventional method is used, for example, using a basic catalyst such as potassium hydroxide, sodium hydroxide, or sodium carbonate in an inert gas. O-co 30″CK
It can be synthesized into J+ by heating. The product is a pale yellow viscous liquid, depending on the molar ratio of isostearic acid.
If the gel properties change, fi, /-2'E, le, it becomes a soft gel, but λ ~ 3 moles of ester tends to give a hard gel. Gel formation work is done using alcohol or an alcohol-containing composition. The desired gel can be obtained by heating and dissolving 2j to yo% or more of isostear monofluoric acid ester to the ioo portion, and then cooling the mixture.
本発明においてはアル;−ルとしてエチルアルコール、
プロピルアルコール、7fルアルコールなどの低級アル
コールが用いられる。In the present invention, ethyl alcohol,
Lower alcohols such as propyl alcohol and 7f alcohol are used.
本発明に係る上記の如きアルコール含水ゲル組成物によ
ればポリグリセリンイソステアリン酸エステル自体が油
付的性質をもつので整髪剤としての機能含有しているか
さらに各種高分子化合物をl′l@又は数種を組合わせ
用いることKよって製品にたとえばよシ大きな整髪力を
もたせてヘアゲルとして用い得、或はローシ冒ン、クリ
ーム、乳液にもよく用いうるようにすることができる。According to the above-mentioned alcohol-containing gel composition according to the present invention, since the polyglycerol isostearate itself has oily properties, it may function as a hair styling agent or may further contain various polymeric compounds. By using a combination of seeds, the product can, for example, have greater hair styling power and can be used as a hair gel, or can be used well in lotions, creams, and emulsions.
かかる高分子化合物としては各種のワックス、流動パラ
フィン、シリコ弄ンオイル、動植物油、エーテルホスフ
ェートやカチオンポリマーをあげることができる。Examples of such polymeric compounds include various waxes, liquid paraffin, silicone oil, animal and vegetable oils, ether phosphates, and cationic polymers.
従って本発明はまたポリグリセリンイソステアリン酸エ
ステルと水及び低級アルコールの外に更にワックス、流
動パラフィン、シリコンオイル。Therefore, in addition to polyglycerol isostearate, water and lower alcohol, the present invention also includes wax, liquid paraffin, and silicone oil.
動植物油、エーテルホス7X−ト、カチオンポリマーか
らなる高分子化合物を一種又は数種含有するアルコール
含水ゲル組成物をも提供するものである。The present invention also provides an alcohol-containing hydrogel composition containing one or more kinds of polymer compounds consisting of animal and vegetable oils, ether phosphates, and cationic polymers.
本発明によればかかる高分子化合物を含有するものも含
有せぬものも、いづれもさきにあげたポリエチレンオキ
シド高級アルコールエーテルなど従来用いられていたゲ
ル化剤を含有しておらずぬめシ感がなく良好な感触を持
ち、特に前記の如き化粧品の基材のほか虫よけクリーム
等の軟膏その他の医薬品の基材として或はまた高分子化
合物を含まぬものはチ璽コレートの柔軟化剤等の食品添
加−として等各種用途に有効に用いることができる〇
〔合成例−1〕
!〜ぶ量体のポリグリセリン!/j Iとイソステアリ
ン酸参3011及び水酸化リチウムt、tpを還流管、
温度計、ガス導入管及び攪拌機を付設した四ツロフラス
コに加えて炭酸ガスを通じながら。According to the present invention, both products containing such a polymer compound and those not containing such a polymer compound do not contain conventionally used gelling agents such as the above-mentioned polyethylene oxide higher alcohol ether and have a slimy feel. It has a good feel and is particularly useful as a base material for cosmetics as mentioned above, as well as for ointments such as insect repellent creams and other pharmaceutical products, or as a softening agent for those that do not contain polymeric compounds. It can be effectively used for various purposes such as food additives such as 〇 [Synthesis Example-1]! ~ Bulk polyglycerin! /j I, isostearic acid 3011 and lithium hydroxide t, tp in a reflux tube,
In addition to a four-way flask equipped with a thermometer, gas inlet tube, and stirrer, carbon dioxide gas was passed through it.
110℃から!”C/10分の割で加熱させてココO℃
に達してから30分間維持して反応を終了し、淡黄色粘
稠液体1701を得た。生成物は次の様な性質を示す。From 110℃! ”C/Heat it for 10 minutes and get it to O℃
After reaching this temperature, the reaction was completed for 30 minutes, and a pale yellow viscous liquid 1701 was obtained. The product exhibits the following properties.
酸 価 0.!
ケン化価 タr
ヒトーaキシル価 air
〔合成例−2〕
j〜を量体のポリグリセリン!/! liとイソステア
リン酸7コoti及び水酸化リチウム!、09を〔合成
例−l〕と同様に反応させると淡黄色粘稠液体/100
1が得られた。生成物は次の様な性質を示す0
酸 @O9参
ケン化価 lココ
ヒドロキシル価 コア0
〔実施例−1〕
31、Jwt@のエタノール水ts@IK合成例−lの
ポリグリセリンイソステアレートυ部を加え、 3゜℃
で均一に溶解させて冷却したところ透明感のあるゲルが
形成された。Acid value 0. ! Saponification value tar Human a-xyl value air [Synthesis Example-2] Polyglycerin with j ~! /! Li, 7-oti isostearate and lithium hydroxide! , 09 is reacted in the same manner as in [Synthesis Example-1] to form a pale yellow viscous liquid/100
1 was obtained. The product exhibits the following properties: 0 Acid @O9 Sansaponification value l Cocohydroxyl value Core 0 [Example-1] 31. Polyglycerol isostearate of Jwt@ ethanol water ts@IK synthesis example-l Add υ part, 3゜℃
When the mixture was uniformly dissolved and cooled, a transparent gel was formed.
このゲルは轄℃迄は安定であ、6.at’cでのチキン
指数はコ、jであシ、整髪剤として使用した場合、ぬめ
り感がなく、整髪力%良好であったO〔実施例−一〕
実施例−/に於いて合成例−lの化合物の代シに合成例
−2のポリグリセリンイソステアレ”−トを同量加えて
調製したゲルは透明感があシ弘S℃でも安定であった0
3℃でのチキソ指数はJ、fであり、ぬめシ感もなく整
髪力も良好であったO〔実施例−3〕
実施例−lで用いた33..1qlt工タノール水tj
部KJjjVllの流動727475部とカチオンポリ
マー (Mark社マーコー) /DO) 、を部を混
合し、これに合成例−7のポリグリセリンインステアレ
ートを加えてSSCで攪拌して溶解し冷却したところ透
明感のあるゲルが形成された。このゲルは弘S℃でも安
定であり、コ℃のチキン指数は30.tであつた。6. This gel is stable up to 50°C. The chicken index at at'c was C, J was Ashi, and when used as a hair styling agent, there was no slimy feeling and the hair styling power% was O [Example-1] Synthesis example in Example-/ The gel prepared by adding the same amount of the polyglycerol isostearate of Synthesis Example-2 to the compound of -l had a transparent feel and was stable even at 0°C.
The thixotropic index at 3°C was J, f, and there was no slimy feeling and the hair styling ability was good [Example-3] 33. .. 1qlt industrial tanol water tj
727,475 parts of cationic polymer (Mark Co., Ltd./DO) were mixed, and the polyglycerol instearate of Synthesis Example 7 was added to this, stirred in SSC to dissolve and cool. A gel with a texture was formed. This gel is stable even at Hiroshima S.C., with a chicken index of 30. It was t.
このゲルは整髪に使用した場合、感触が曳く、整髪力も
良好であった。When this gel was used for hair styling, it had a smooth feel and good hair styling ability.
実施例−ノで用いた13,3%エタノール水tj部にサ
メの肝油たるスタフ2フ5部とエーテルホス7エート(
ヘキスト社ホスタフアットKOJto)z部を混合し、
これに合成例−lのポリグリセリンイソステアレートを
加えてお℃で攪拌して溶解し。To tj parts of the 13.3% ethanol water used in Example No. 2, 5 parts of shark liver oil Stuff and ether phos 7ate (
Hoechst Co., Ltd. Hostafut KOJto) z part is mixed,
The polyglycerol isostearate of Synthesis Example 1 was added to this and dissolved by stirring at °C.
冷却したところ透明感のあるゲルが形成された。Upon cooling, a transparent gel was formed.
このゲルは0℃でも安定であり、x”cのチキソ指数は
コ、7であった。このゲルは整髪に使用した場合、感触
が曳く、乾かした場合、冷水ではベトっかず、シャンプ
ーでおち申すかうた〇
〔実施例−j〕
実施例−参に於いてスクワランの代シに椿油を用いた場
合、同様のゲルが形成された。このゲルは轄℃でも安定
でTo、6.g’cのチキソ指数はコ、りであった。こ
のゲルを整髪に使用した場合、ぬめシ感がなく、乾かし
た場合、冷水でベトっかず。This gel was stable even at 0°C, and the thixotropic index of [Example-j] When camellia oil was used as a substitute for squalane in Example-3, a similar gel was formed. The thixotropic index of C was 0. When this gel was used for styling hair, it did not feel slimy, and when dried, it did not become sticky with cold water.
シャンプーでおちやすかった。It was easy to calm down with shampoo.
出願人代理人 猪 股 清Applicant's agent Kiyoshi Inomata
Claims (1)
低級アルコールを含むアルコール含水ゲル組成物0 コ、ポリグリ令すンイソステアリン駿エステルと水及び
低級アルコールを含み、更にワックス。 流動パラフィン、シリコンオイル、動植物油、エーテル
ホスフェート、カチオンポリマーからなる高分子化合物
を1種又は数種含有するアルコール含水ゲル組成物0 3、ポリグリセリンイソステアリン酸エステルはj−を
量体のグリセリンからなるポリグリセリンに対して屹ル
比/S−Jのイソステアリン酸を反応させて見られた化
合物である特許請求の範囲第1項又は第2項記載のアル
コール含水ゲル組成1[Scope of Claims] 1. An alcohol-containing hydrogel composition containing polyglycerin isostearate, water and a lower alcohol; and further comprising a wax. Alcohol-containing gel composition containing one or more types of high molecular compounds consisting of liquid paraffin, silicone oil, animal and vegetable oils, ether phosphates, and cationic polymers 03, polyglycerol isostearate ester consists of j-mer glycerin Alcohol-containing hydrogel composition 1 according to claim 1 or 2, which is a compound obtained by reacting isostearic acid with a ratio of /S-J to polyglycerin.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP56164451A JPS5864128A (en) | 1981-10-15 | 1981-10-15 | Alcohol-containing aqueous gel composition |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP56164451A JPS5864128A (en) | 1981-10-15 | 1981-10-15 | Alcohol-containing aqueous gel composition |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5864128A true JPS5864128A (en) | 1983-04-16 |
| JPH0152051B2 JPH0152051B2 (en) | 1989-11-07 |
Family
ID=15793416
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP56164451A Granted JPS5864128A (en) | 1981-10-15 | 1981-10-15 | Alcohol-containing aqueous gel composition |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS5864128A (en) |
Cited By (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6185328A (en) * | 1984-10-02 | 1986-04-30 | Kao Corp | Percutaneous absorption promoter and external preparation for skin containing same |
| JPS61137810A (en) * | 1984-12-07 | 1986-06-25 | Nonogawa Shoji:Kk | Cosmetic |
| US4751075A (en) * | 1986-01-08 | 1988-06-14 | Redken Laboratories, Inc. | Anhydrous cosmetic compositions for thermal skin treatments |
| JP2009021853A (en) * | 2007-07-12 | 2009-01-29 | Seiko Instruments Inc | Piezoelectric vibrator manufacturing method, piezoelectric vibrator, oscillator, electronic device, and radio timepiece |
| JP2010087574A (en) * | 2008-09-29 | 2010-04-15 | Nippon Dempa Kogyo Co Ltd | Piezoelectric vibration piece and piezoelectric device |
| JP2010136419A (en) * | 2010-01-22 | 2010-06-17 | Seiko Epson Corp | Tuning fork type piezoelectric vibrator |
| US8063546B2 (en) | 2008-02-20 | 2011-11-22 | Seiko Epson Corporation | Vibrator comprising two X-cut crystal substrates with an intermediate electrode |
| US8134284B2 (en) | 2008-05-22 | 2012-03-13 | Nihon Dempa Kogyo Co., Ltd. | Tuning-fork type piezoelectric vibrating pieces having similarly shaped vibrating-root and supporting root portions |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA2560030C (en) | 2005-11-24 | 2013-11-12 | Sulzer Metco Ag | A thermal spraying material, a thermally sprayed coating, a thermal spraying method an also a thermally coated workpiece |
-
1981
- 1981-10-15 JP JP56164451A patent/JPS5864128A/en active Granted
Cited By (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6185328A (en) * | 1984-10-02 | 1986-04-30 | Kao Corp | Percutaneous absorption promoter and external preparation for skin containing same |
| JPS61137810A (en) * | 1984-12-07 | 1986-06-25 | Nonogawa Shoji:Kk | Cosmetic |
| US4751075A (en) * | 1986-01-08 | 1988-06-14 | Redken Laboratories, Inc. | Anhydrous cosmetic compositions for thermal skin treatments |
| JP2009021853A (en) * | 2007-07-12 | 2009-01-29 | Seiko Instruments Inc | Piezoelectric vibrator manufacturing method, piezoelectric vibrator, oscillator, electronic device, and radio timepiece |
| US8063546B2 (en) | 2008-02-20 | 2011-11-22 | Seiko Epson Corporation | Vibrator comprising two X-cut crystal substrates with an intermediate electrode |
| US8134284B2 (en) | 2008-05-22 | 2012-03-13 | Nihon Dempa Kogyo Co., Ltd. | Tuning-fork type piezoelectric vibrating pieces having similarly shaped vibrating-root and supporting root portions |
| JP2010087574A (en) * | 2008-09-29 | 2010-04-15 | Nippon Dempa Kogyo Co Ltd | Piezoelectric vibration piece and piezoelectric device |
| JP2010136419A (en) * | 2010-01-22 | 2010-06-17 | Seiko Epson Corp | Tuning fork type piezoelectric vibrator |
Also Published As
| Publication number | Publication date |
|---|---|
| JPH0152051B2 (en) | 1989-11-07 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE69231526T2 (en) | SHAVERS | |
| US4528111A (en) | Shaving cream gel containing interpolymer reaction product of selected cationic polymers and anionic polymers | |
| CN102793634A (en) | Hair styling composition | |
| DE69532512T2 (en) | FIXED SHAVING COMPOSITIONS | |
| JPS58162632A (en) | Novel polyether derivative and emulsion containing same | |
| JPH0152051B2 (en) | ||
| WO1988001876A1 (en) | Post-foaming gel containing certain dialkanolamide or monoalkanolamide | |
| JPS6152804B2 (en) | ||
| CA2315732C (en) | Silicone oil emulsion stabilized with soap | |
| JPS6140202B2 (en) | ||
| JPH0272111A (en) | Post-foaming shaving gel composition | |
| JP4800681B2 (en) | Gelling agent and gel composition | |
| BR112020002821B1 (en) | EMULSIFYING SYSTEM, PERSONAL CARE PRODUCT, METHOD AND USE | |
| JPH0881326A (en) | Aerosol-type cosmetic | |
| JPS6019728B2 (en) | Improved cream skin cosmetics | |
| US20220235274A1 (en) | Oil in Water Wax Emulsion Composition | |
| JP3526456B2 (en) | Esterification product and cosmetic containing the same | |
| JP2016155819A (en) | NOVEL BASE, COSMETIC COMPOSITION CONTAINING THE SAME AND COSMETIC COMPOSITION CONTAINING THE SAME | |
| JP2004131384A (en) | Transparent lipstick | |
| JP3000396B2 (en) | Translucent cosmetics | |
| JPH11286420A (en) | Hair cosmetic | |
| JPS6122005A (en) | Oil-in-water emulsion type cosmetic | |
| JP3698665B2 (en) | Cosmetics | |
| JPH11152205A (en) | Lower alcohol-free aqueous gel composition | |
| JP2708691B2 (en) | Aerosol composition containing powder |