JPH036180B2 - - Google Patents
Info
- Publication number
- JPH036180B2 JPH036180B2 JP28493085A JP28493085A JPH036180B2 JP H036180 B2 JPH036180 B2 JP H036180B2 JP 28493085 A JP28493085 A JP 28493085A JP 28493085 A JP28493085 A JP 28493085A JP H036180 B2 JPH036180 B2 JP H036180B2
- Authority
- JP
- Japan
- Prior art keywords
- parts
- weight
- fatty acid
- composition
- gel
- 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.)
- Expired
Links
- 239000000203 mixture Substances 0.000 claims description 29
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 16
- 239000000194 fatty acid Substances 0.000 claims description 16
- 229930195729 fatty acid Natural products 0.000 claims description 16
- -1 aliphatic alcohols Chemical class 0.000 claims description 11
- 125000004432 carbon atom Chemical group C* 0.000 claims description 9
- 239000004375 Dextrin Substances 0.000 claims description 7
- 229920001353 Dextrin Polymers 0.000 claims description 7
- 235000019425 dextrin Nutrition 0.000 claims description 7
- 150000004665 fatty acids Chemical class 0.000 claims description 7
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 claims description 6
- 125000004122 cyclic group Chemical group 0.000 claims description 6
- 239000004205 dimethyl polysiloxane Substances 0.000 claims description 6
- 235000013870 dimethyl polysiloxane Nutrition 0.000 claims description 6
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 claims description 6
- 150000002148 esters Chemical class 0.000 claims description 5
- 229920002545 silicone oil Polymers 0.000 description 9
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
- 239000002537 cosmetic Substances 0.000 description 3
- 238000001879 gelation Methods 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 239000003921 oil Substances 0.000 description 3
- 229920001296 polysiloxane Polymers 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- 125000002252 acyl group Chemical group 0.000 description 2
- LFYJSSARVMHQJB-QIXNEVBVSA-N bakuchiol Chemical compound CC(C)=CCC[C@@](C)(C=C)\C=C\C1=CC=C(O)C=C1 LFYJSSARVMHQJB-QIXNEVBVSA-N 0.000 description 2
- GLYJVQDYLFAUFC-UHFFFAOYSA-N butyl hexadecanoate Chemical compound CCCCCCCCCCCCCCCC(=O)OCCCC GLYJVQDYLFAUFC-UHFFFAOYSA-N 0.000 description 2
- 235000013312 flour Nutrition 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 239000005457 ice water Substances 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 239000000377 silicon dioxide Substances 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
- DNIAPMSPPWPWGF-GSVOUGTGSA-N (R)-(-)-Propylene glycol Chemical compound C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-N 0.000 description 1
- QMMJWQMCMRUYTG-UHFFFAOYSA-N 1,2,4,5-tetrachloro-3-(trifluoromethyl)benzene Chemical compound FC(F)(F)C1=C(Cl)C(Cl)=CC(Cl)=C1Cl QMMJWQMCMRUYTG-UHFFFAOYSA-N 0.000 description 1
- UMHYVXGZRGOICM-AUYXYSRISA-N 2-[(z)-octadec-9-enoyl]oxypropyl (z)-octadec-9-enoate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OCC(C)OC(=O)CCCCCCC\C=C/CCCCCCCC UMHYVXGZRGOICM-AUYXYSRISA-N 0.000 description 1
- HIQIXEFWDLTDED-UHFFFAOYSA-N 4-hydroxy-1-piperidin-4-ylpyrrolidin-2-one Chemical compound O=C1CC(O)CN1C1CCNCC1 HIQIXEFWDLTDED-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- XMSXQFUHVRWGNA-UHFFFAOYSA-N Decamethylcyclopentasiloxane Chemical compound C[Si]1(C)O[Si](C)(C)O[Si](C)(C)O[Si](C)(C)O[Si](C)(C)O1 XMSXQFUHVRWGNA-UHFFFAOYSA-N 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- CMBYOWLFQAFZCP-UHFFFAOYSA-N Hexyl dodecanoate Chemical compound CCCCCCCCCCCC(=O)OCCCCCC CMBYOWLFQAFZCP-UHFFFAOYSA-N 0.000 description 1
- GORMSINSWZJIKL-UHFFFAOYSA-N [3-(2-ethylhexanoyloxy)-2,2-dimethylpropyl] 2-ethylhexanoate Chemical compound CCCCC(CC)C(=O)OCC(C)(C)COC(=O)C(CC)CCCC GORMSINSWZJIKL-UHFFFAOYSA-N 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- DHAZIUXMHRHVMP-UHFFFAOYSA-N butyl tetradecanoate Chemical compound CCCCCCCCCCCCCC(=O)OCCCC DHAZIUXMHRHVMP-UHFFFAOYSA-N 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 239000006071 cream Substances 0.000 description 1
- SASYSVUEVMOWPL-NXVVXOECSA-N decyl oleate Chemical compound CCCCCCCCCCOC(=O)CCCCCCC\C=C/CCCCCCCC SASYSVUEVMOWPL-NXVVXOECSA-N 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 150000002194 fatty esters Chemical class 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000003205 fragrance Substances 0.000 description 1
- 239000003349 gelling agent Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229940100463 hexyl laurate Drugs 0.000 description 1
- 239000012456 homogeneous solution Substances 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 239000011256 inorganic filler Substances 0.000 description 1
- 229910003475 inorganic filler Inorganic materials 0.000 description 1
- XUGNVMKQXJXZCD-UHFFFAOYSA-N isopropyl palmitate Chemical compound CCCCCCCCCCCCCCCC(=O)OC(C)C XUGNVMKQXJXZCD-UHFFFAOYSA-N 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- 230000005923 long-lasting effect Effects 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 229940105132 myristate Drugs 0.000 description 1
- 229940078812 myristyl myristate Drugs 0.000 description 1
- JXTPJDDICSTXJX-UHFFFAOYSA-N n-Triacontane Natural products CCCCCCCCCCCCCCCCCCCCCCCCCCCCCC JXTPJDDICSTXJX-UHFFFAOYSA-N 0.000 description 1
- HMMGMWAXVFQUOA-UHFFFAOYSA-N octamethylcyclotetrasiloxane Chemical compound C[Si]1(C)O[Si](C)(C)O[Si](C)(C)O[Si](C)(C)O1 HMMGMWAXVFQUOA-UHFFFAOYSA-N 0.000 description 1
- 125000000913 palmityl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229940010310 propylene glycol dioleate Drugs 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 229940032094 squalane Drugs 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- TUNFSRHWOTWDNC-UHFFFAOYSA-N tetradecanoic acid Chemical compound CCCCCCCCCCCCCC(O)=O TUNFSRHWOTWDNC-UHFFFAOYSA-N 0.000 description 1
- DZKXJUASMGQEMA-UHFFFAOYSA-N tetradecyl tetradecanoate Chemical compound CCCCCCCCCCCCCCOC(=O)CCCCCCCCCCCCC DZKXJUASMGQEMA-UHFFFAOYSA-N 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- LADGBHLMCUINGV-UHFFFAOYSA-N tricaprin Chemical compound CCCCCCCCCC(=O)OCC(OC(=O)CCCCCCCCC)COC(=O)CCCCCCCCC LADGBHLMCUINGV-UHFFFAOYSA-N 0.000 description 1
- VLPFTAMPNXLGLX-UHFFFAOYSA-N trioctanoin Chemical compound CCCCCCCC(=O)OCC(OC(=O)CCCCCCC)COC(=O)CCCCCCC VLPFTAMPNXLGLX-UHFFFAOYSA-N 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
- A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
- A61K8/73—Polysaccharides
- A61K8/732—Starch; Amylose; Amylopectin; 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
- A61K8/02—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
- 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
- A61K8/37—Esters of carboxylic acids
-
- 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
- A61K8/84—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions otherwise than those involving only carbon-carbon unsaturated bonds
- A61K8/89—Polysiloxanes
- A61K8/891—Polysiloxanes saturated, e.g. dimethicone, phenyl trimethicone, C24-C28 methicone or stearyl dimethicone
-
- 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)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Epidemiology (AREA)
- Birds (AREA)
- Emergency Medicine (AREA)
- Dermatology (AREA)
- Chemical & Material Sciences (AREA)
- Dispersion Chemistry (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Medicinal Preparation (AREA)
- Cosmetics (AREA)
Description
(産業上の利用分野〕
本発明はゲル状組成物、特にはシリカなどの充
填剤を使用しない、化粧品用基材などに有用とさ
れるシリコーンオイルを主材とするゲル状組成物
に関するものである。
(従来の技術)
化粧品用、医療用のペースト、クリーム、プレ
ス状組成物などには各種のシリコーンオイルが添
加配合されているが、シリコーン組成物を基材と
する利用例は少ない。
これはシリコオーオイルをゲル状物とするには
無機質充填剤としての疎水性シリカ、ベントンな
どの増粘剤の添加が必要であり、使用するシリコ
ーオイルも25℃における粘度が100cS以上である
比較的高粘度のものとする必要があるために、こ
のようにして得られたゲル状物を皮膚表面に塗布
した場合には伸度感が重く、また揮発分が殆んど
ないのでべたつき感が長期にわたつて残留する不
利があるからとされている。
したがつて、これらの欠点を解決した低粘度で
揮発性に富むシリコーンを主剤とするゲル状組成
物が待望されている。
(発明の構成)
本発明は上記したような不利を解決したシリコ
ーン系のゲル状組成物に関するものであり。これ
は、(1)式
示される環状ジメチルポリシロキサン30〜90重量
部、(2)炭素数8〜24の脂肪酸と炭素数1〜24の脂
肪酸アルコールとのエステルまたは炭素数10〜40
の脂肪族炭化水素から選択される1種または2種
以上の混合物5〜50重量部、(3)デキストリン脂肪
酸エステル5〜30重量部とからなることを特徴と
するものである。
すなわち、本発明者らは等に化粧品用、医療用
などに有用とされるシリコーンオイルを主剤とす
るゲル状組成物について種々検討した結果、シリ
コーンオイルとして上記した式で示される環状ジ
メチルポリシロキサンを使用すると共に、このゲ
ル化剤として高級脂肪酸の脂肪族アルコールとの
エステルまたは脂肪族炭化水素とデキストリン脂
肪酸エステルを使用すると所期のゲル状組成物が
容易に得られ、このゲル状組成物はこれを皮膚な
どに塗布した場合に進展性が軽快で使用感もさつ
ぱりしており、塗布後は環状ジメチルポリシロキ
サンが蒸発するために濡れ感覚が何時までも残る
ことがないということを確認して本発明を完成さ
せた。
本発明のゲル状組成物を構成する第1成分とし
てのシリコーンオイルは、式
で示される環状ジメチルポリシロキサンとされる
が、このものはこれを含有するゲル状組成物を使
用後に発揮するものであることが望ましいので、
このn値は3〜6のものとされる。なお、このも
のは1種の使用でもよく、2種以上の混合物であ
つてもよいが、この使用量はゲル状組成物100重
量部におけるこの第1成分の量が30重量部以下で
は他成分が多くなりすぎて本組成物に期待される
軽快な進展性を乏しくなるし、べたつき感も増大
し、90重量部以上とすると十分なゲル化に至れな
くなるので、30〜90重量部の範囲とすることが必
要とされるが、この好ましい範囲は40〜8重量部
とされる。
また、この組成物における第2成分は前記した
ように炭素数が8〜20の高級脂肪酸と炭素数1〜
24の脂肪族アルコールとのエステルまたは炭素数
10〜40の脂肪族炭化水素とされ、これについては
ミリスチン酸イソプロピル、ミリスチン酸ブチ
ル、ミリスチン酸ミリスチル、ミリスチン酸オク
チルデシル、イソオクチル酸セチル、オレイル酸
デシル、ステアリン酸ブチル、ラウリン酸ヘキシ
ル、パルミチン酸イソプロピル、パルミチン酸ブ
チルなどの高級脂肪酸モノエステル、ジオレイン
酸プロピレングリコール、ジ−2−エチルヘキサ
ン酸ネオペンチルグリコールなどの高級脂肪酸ジ
エステル、カプリル酸トリグリセリド、カプリン
酸トリグリセリドなどの高級脂肪酸トリエステル
など、さらにはスクワラン、アイソパー〔エクソ
ン化学(株)製、脂肪族炭化水素系溶剤の商品名〕な
どが例示されるが、これらはその1種で使用して
も2種以上の混合物であつてもよい。なお、この
第2成分の使用量はゲル化組成物100重量部中に
おけるこの成2成分の量が5重量部以下では第1
成分としてのシリコーンオイルがゲル化するまで
には至らず、50重量部以上とすると得られるゲル
状組成物が軽快な伸展性の乏しいものとなり、べ
たつき感も増大するので5〜50重量部の範囲とす
る必要があるが、この好ましい範囲は7〜45重量
部とされる。
つぎにこのゲル状組成物における第3成分とし
てのデキストリン脂肪酸エステルは例えば構造式
が次式
で示され、Aは水素原子または炭素数8〜20のの
アシル基で全Aモル数の50%以上はアシル基、l
は20〜30とされるものであり、この使用量はゲル
状組成物100重量部中におけるこの第3成分の量
が5重量部以下ではシリコールオイルのゲル化が
進まず、30重部以上とすると得られる組成物が固
くなりすぎて伸展性の乏しいものとなるので5〜
30重量部の範囲とするることが必要とされるが、
この好ましい範囲は7〜25重量部とされる。
本発明のゲル状組成物は上記した第1成分〜第
3成分の所定量を均一に混合することによつて得
ることができるが、この混合は50〜100℃で行う
ことがよく、例えば100℃以下で加温撹拌も行つ
て前記した脂肪酸エステルまたは脂肪族炭化水素
およびデキストリン樹脂エステルをシリコーンオ
イルに均一に溶解してから冷却すれば目的とする
均質なゲル状組成物を得ることができる。なお、
この組成物に各種の油性剤、香料、医薬用成分、
酸化防止剤、顔料、染料などを添加することは本
発明の組成物の特性に大きな変更を来たさない範
囲であれば任意とされる。
つぎに本発明の実施例をあげるが、例中の部は
重量部を、また粘度は25℃での測定値を示したも
のである。
実施例 1〜10
第1表に示した量のオクタメチルシクロテトラ
シロキサン・KF994(信越化学工業(株)製商品名〕
およびデカメチルシクロペンタシロキサンKF995
〔同社製商品名〕に第1表に示した種類および量
の高級脂肪酸エステルまたは脂肪族炭化水素なら
びに第1表に示した量のデキストリン脂肪酸エス
テル・レオパールKL〔千葉製粉(株)製商品名〕を添
加し、この総量300gを500mlの硬質ガラスフラス
コ中に投入し、60〜70℃で撹拌して均一溶液とな
つたことを確認して撹拌を停止し、氷水浴で急冷
したところ、均一なゲル状組成物が得られたの
で、この組成物についての稠度、離油度をJIS
K2220に準拠した方法で測定したところ第1表に
併記したとうりの結果が得られた。
(Industrial Application Field) The present invention relates to a gel composition, particularly a gel composition based on silicone oil that does not use fillers such as silica and is useful as a base material for cosmetics. (Prior art) Various silicone oils are added to pastes, creams, pressed compositions, etc. for cosmetics and medical purposes, but there are few examples of use of silicone compositions as a base material. To make silico-oil into a gel, it is necessary to add thickeners such as hydrophobic silica and bentone as inorganic fillers, and the silico-oil used also has a viscosity of 100 cS or more at 25°C. Because it needs to have a high viscosity, when the gel-like material obtained in this way is applied to the skin surface, it feels heavy and has a long-lasting sticky feeling because it has almost no volatile content. Accordingly, there has been a long-awaited need for a gel-like composition based on silicone, which has low viscosity and high volatility and solves these drawbacks. (Structure of the Invention ) The present invention relates to a silicone-based gel composition that solves the above-mentioned disadvantages. 30 to 90 parts by weight of the indicated cyclic dimethyl polysiloxane, (2) an ester of a fatty acid having 8 to 24 carbon atoms and a fatty acid alcohol having 1 to 24 carbon atoms or 10 to 40 carbon atoms;
(3) dextrin fatty acid ester (5 to 30 parts by weight). That is, as a result of various studies conducted by the present inventors on gel compositions based on silicone oil, which are useful for cosmetics, medical applications, etc., we have found that cyclic dimethylpolysiloxane represented by the above formula is used as the silicone oil. In addition, if an ester of a higher fatty acid with an aliphatic alcohol or an aliphatic hydrocarbon and a dextrin fatty acid ester is used as the gelling agent, the desired gel composition can be easily obtained. We have confirmed that when applied to the skin, the spread is light and the feeling is refreshing, and the cyclic dimethylpolysiloxane evaporates after application, so the wet feeling does not remain for any length of time. The present invention was completed. The silicone oil as the first component constituting the gel composition of the present invention has the formula It is said to be a cyclic dimethylpolysiloxane represented by, but it is desirable that this product exhibits its properties after using a gel composition containing it.
This n value is set to 3 to 6. Note that this substance may be used alone or in a mixture of two or more types, but if the amount of this first component is 30 parts by weight or less in 100 parts by weight of the gel composition, other components may be used. If the amount exceeds 90 parts by weight, it will impair the easy spreadability expected of this composition, increase the stickiness, and if it exceeds 90 parts by weight, sufficient gelation will not be achieved. The preferred range is 40 to 8 parts by weight. Further, as described above, the second component in this composition is a higher fatty acid having 8 to 20 carbon atoms and a higher fatty acid having 1 to 20 carbon atoms.
Esters with aliphatic alcohols of 24 or carbon numbers
10 to 40 aliphatic hydrocarbons, including isopropyl myristate, butyl myristate, myristyl myristate, octyldecyl myristate, cetyl isooctylate, decyl oleate, butyl stearate, hexyl laurate, and isopropyl palmitate. , higher fatty acid monoesters such as butyl palmitate, higher fatty acid diesters such as propylene glycol dioleate, neopentyl glycol di-2-ethylhexanoate, higher fatty acid triesters such as caprylic acid triglyceride and capric acid triglyceride, and even squalane. , Isopar [manufactured by Exxon Chemical Co., Ltd., trade name of aliphatic hydrocarbon solvent], etc., and these may be used alone or in a mixture of two or more. Note that if the amount of this second component used is 5 parts by weight or less in 100 parts by weight of the gelling composition, the amount of the second component used is less than the first amount.
If the silicone oil as a component does not gel, and if it exceeds 50 parts by weight, the resulting gel-like composition will have poor light extensibility and increase stickiness, so use a range of 5 to 50 parts by weight. The preferred range is 7 to 45 parts by weight. Next, the dextrin fatty acid ester as the third component in this gel composition has, for example, the following structural formula: A is a hydrogen atom or an acyl group having 8 to 20 carbon atoms, and 50% or more of the total number of moles of A is an acyl group, l
is said to be 20 to 30, and if the amount of this third component is less than 5 parts by weight in 100 parts by weight of the gel composition, gelation of the silicone oil will not proceed; If this is done, the resulting composition will be too hard and have poor extensibility, so
A range of 30 parts by weight is required, but
The preferred range is 7 to 25 parts by weight. The gel composition of the present invention can be obtained by uniformly mixing predetermined amounts of the first to third components described above, but this mixing is preferably carried out at 50 to 100°C, for example at 100°C. The desired homogeneous gel composition can be obtained by uniformly dissolving the aforementioned fatty acid ester or aliphatic hydrocarbon and dextrin resin ester in silicone oil by heating and stirring at a temperature below .degree. C. and then cooling. In addition,
This composition includes various oily agents, fragrances, pharmaceutical ingredients,
Addition of antioxidants, pigments, dyes, etc. is optional as long as it does not significantly change the properties of the composition of the present invention. Next, examples of the present invention will be given, in which parts are parts by weight, and viscosity is a value measured at 25°C. Examples 1 to 10 Octamethylcyclotetrasiloxane KF994 (trade name manufactured by Shin-Etsu Chemical Co., Ltd.) in the amounts shown in Table 1
and decamethylcyclopentasiloxane KF995
[Product name manufactured by the company] higher fatty acid ester or aliphatic hydrocarbon of the type and amount shown in Table 1 and dextrin fatty acid ester Leopard KL in the amount shown in Table 1 [Product name manufactured by Chiba Flour Milling Co., Ltd.] The total amount of 300g was put into a 500ml hard glass flask, stirred at 60 to 70℃, and after confirming that it had become a homogeneous solution, stirring was stopped and quenched in an ice water bath. Since a gel-like composition was obtained, the consistency and oil separation degree of this composition were determined by JIS.
When measured using a method based on K2220, the results shown in Table 1 were obtained.
【表】
比較例
実施例で使用した環状ジメチルポリシロキサ
ン・KF994またはKF995 270部に、デキストリン
脂肪エステル・レオパールKL〔千葉製粉(株)製商品
名〕30部を添加し、500mlの硬化ガラスフラスコ
中で60〜70℃に撹拌したが、レオパールKLはシ
リコーンオイルに均一に溶解せず、撹拌後に氷水
浴で急冷したものはレオパールKLが沈殿となり、
全くゲル化は認められなかつた。[Table] Comparative Example To 270 parts of the cyclic dimethylpolysiloxane KF994 or KF995 used in the example, 30 parts of dextrin fatty ester Leopard KL [trade name manufactured by Chiba Flour Milling Co., Ltd.] was added, and the mixture was placed in a 500 ml hardened glass flask. Although the mixture was stirred at 60 to 70℃, Leopard KL did not dissolve uniformly in the silicone oil, and when it was rapidly cooled in an ice water bath after stirring, Leopard KL precipitated.
No gelation was observed at all.
Claims (1)
30〜90重量部、 (2) 炭素数8〜24の脂肪酸と炭素数1〜24脂肪族
アルコールとのエステルまたは炭素数10〜40の
脂肪族炭化水素から選ばれる1種または2種以
上の混合物 5〜50重量部、 (3) デキストリン脂肪酸エステル 5〜30重量部 とからなることを特徴とするゲル状組成物。[Claims] 1 (1) Formula Cyclic dimethylpolysiloxane represented by
30 to 90 parts by weight, (2) One or more mixtures selected from esters of fatty acids with 8 to 24 carbon atoms and aliphatic alcohols with 1 to 24 carbon atoms, or aliphatic hydrocarbons with 10 to 40 carbon atoms. (3) 5 to 30 parts by weight of dextrin fatty acid ester.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP28493085A JPS62143971A (en) | 1985-12-17 | 1985-12-17 | Gelatinous composition |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP28493085A JPS62143971A (en) | 1985-12-17 | 1985-12-17 | Gelatinous composition |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS62143971A JPS62143971A (en) | 1987-06-27 |
JPH036180B2 true JPH036180B2 (en) | 1991-01-29 |
Family
ID=17684897
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP28493085A Granted JPS62143971A (en) | 1985-12-17 | 1985-12-17 | Gelatinous composition |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS62143971A (en) |
Families Citing this family (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH072631B2 (en) * | 1987-03-06 | 1995-01-18 | テルモ株式会社 | Gel composition |
JP2887485B2 (en) * | 1989-08-09 | 1999-04-26 | 花王株式会社 | Oily cosmetics |
JP2631772B2 (en) * | 1991-02-27 | 1997-07-16 | 信越化学工業株式会社 | Novel silicone polymer and paste-like silicone composition having water dispersibility using the same |
US5919437A (en) * | 1996-05-24 | 1999-07-06 | Colgate-Palmolive Company | Cosmetic cream composition containing silicone gel material |
JP4688291B2 (en) * | 2000-12-28 | 2011-05-25 | 株式会社コーセー | Oil makeup cosmetics |
EP1935924B1 (en) | 2002-09-12 | 2012-06-06 | Shin-Etsu Chemical Company, Ltd. | Pasty composition, and cosmetic preparation containing the same |
JP6215719B2 (en) | 2014-01-23 | 2017-10-18 | 信越化学工業株式会社 | Cosmetics |
JP6432244B2 (en) * | 2014-09-24 | 2018-12-05 | 富士ゼロックス株式会社 | Electrophotographic photosensitive member, process cartridge, and image forming apparatus |
JP6285381B2 (en) | 2015-03-13 | 2018-02-28 | 信越化学工業株式会社 | Gel paste composition and cosmetics using the gel paste composition |
JP2023057598A (en) | 2021-10-12 | 2023-04-24 | 信越化学工業株式会社 | Organoalkoxysilane-containing composition and production method of the same, and water absorption-preventive agent |
-
1985
- 1985-12-17 JP JP28493085A patent/JPS62143971A/en active Granted
Also Published As
Publication number | Publication date |
---|---|
JPS62143971A (en) | 1987-06-27 |
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