KR900013941A - 퍼플루오로폴리에테르 안정유액 - Google Patents
퍼플루오로폴리에테르 안정유액 Download PDFInfo
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- 239000000839 emulsion Substances 0.000 title claims 16
- 239000010702 perfluoropolyether Substances 0.000 title claims 9
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims 9
- 229910052731 fluorine Inorganic materials 0.000 claims 6
- 239000000203 mixture Substances 0.000 claims 5
- 150000001875 compounds Chemical class 0.000 claims 4
- 239000004094 surface-active agent Substances 0.000 claims 4
- 239000002904 solvent Substances 0.000 claims 3
- 150000005846 sugar alcohols Polymers 0.000 claims 3
- 125000000217 alkyl group Chemical group 0.000 claims 2
- 150000001720 carbohydrates Chemical class 0.000 claims 2
- 125000004432 carbon atom Chemical group C* 0.000 claims 2
- 239000003995 emulsifying agent Substances 0.000 claims 2
- 125000001153 fluoro group Chemical group F* 0.000 claims 2
- 150000004676 glycans Chemical class 0.000 claims 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 2
- -1 oxytrifluoromethyltrifluoro ethylene Chemical group 0.000 claims 2
- 125000005010 perfluoroalkyl group Chemical group 0.000 claims 2
- 229920001282 polysaccharide Polymers 0.000 claims 2
- 239000005017 polysaccharide Substances 0.000 claims 2
- AGNTUZCMJBTHOG-UHFFFAOYSA-N 3-[3-(2,3-dihydroxypropoxy)-2-hydroxypropoxy]propane-1,2-diol Chemical compound OCC(O)COCC(O)COCC(O)CO AGNTUZCMJBTHOG-UHFFFAOYSA-N 0.000 claims 1
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 claims 1
- FBPFZTCFMRRESA-KVTDHHQDSA-N D-Mannitol Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-KVTDHHQDSA-N 0.000 claims 1
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 claims 1
- 229930091371 Fructose Natural products 0.000 claims 1
- RFSUNEUAIZKAJO-ARQDHWQXSA-N Fructose Chemical compound OC[C@H]1O[C@](O)(CO)[C@@H](O)[C@@H]1O RFSUNEUAIZKAJO-ARQDHWQXSA-N 0.000 claims 1
- 239000005715 Fructose Substances 0.000 claims 1
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 claims 1
- 229930195725 Mannitol Natural products 0.000 claims 1
- 229930006000 Sucrose Natural products 0.000 claims 1
- CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 claims 1
- TVXBFESIOXBWNM-UHFFFAOYSA-N Xylitol Natural products OCCC(O)C(O)C(O)CCO TVXBFESIOXBWNM-UHFFFAOYSA-N 0.000 claims 1
- 150000001298 alcohols Chemical class 0.000 claims 1
- 125000000129 anionic group Chemical group 0.000 claims 1
- WQZGKKKJIJFFOK-VFUOTHLCSA-N beta-D-glucose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 claims 1
- 229910052799 carbon Inorganic materials 0.000 claims 1
- 125000002091 cationic group Chemical group 0.000 claims 1
- 239000002537 cosmetic Substances 0.000 claims 1
- 235000013681 dietary sucrose Nutrition 0.000 claims 1
- GPLRAVKSCUXZTP-UHFFFAOYSA-N diglycerol Chemical compound OCC(O)COCC(O)CO GPLRAVKSCUXZTP-UHFFFAOYSA-N 0.000 claims 1
- 150000002170 ethers Chemical class 0.000 claims 1
- 239000012530 fluid Substances 0.000 claims 1
- 239000008103 glucose Substances 0.000 claims 1
- 235000001727 glucose Nutrition 0.000 claims 1
- 150000002334 glycols Chemical class 0.000 claims 1
- 239000004816 latex Substances 0.000 claims 1
- 229920000126 latex Polymers 0.000 claims 1
- 239000000594 mannitol Substances 0.000 claims 1
- 235000010355 mannitol Nutrition 0.000 claims 1
- HEBKCHPVOIAQTA-UHFFFAOYSA-N meso ribitol Natural products OCC(O)C(O)C(O)CO HEBKCHPVOIAQTA-UHFFFAOYSA-N 0.000 claims 1
- 239000000600 sorbitol Substances 0.000 claims 1
- 235000010356 sorbitol Nutrition 0.000 claims 1
- 239000003381 stabilizer Substances 0.000 claims 1
- 229960004793 sucrose Drugs 0.000 claims 1
- 235000000346 sugar Nutrition 0.000 claims 1
- 150000008163 sugars Chemical class 0.000 claims 1
- JYKSTGLAIMQDRA-UHFFFAOYSA-N tetraglycerol Chemical compound OCC(O)CO.OCC(O)CO.OCC(O)CO.OCC(O)CO JYKSTGLAIMQDRA-UHFFFAOYSA-N 0.000 claims 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims 1
- 239000000811 xylitol Substances 0.000 claims 1
- HEBKCHPVOIAQTA-SCDXWVJYSA-N xylitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)CO HEBKCHPVOIAQTA-SCDXWVJYSA-N 0.000 claims 1
- 235000010447 xylitol Nutrition 0.000 claims 1
- 229960002675 xylitol Drugs 0.000 claims 1
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- C08J3/00—Processes of treating or compounding macromolecular substances
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- A61K8/69—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing fluorine
- A61K8/70—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing fluorine containing perfluoro groups, e.g. perfluoroethers
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- A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
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Abstract
내용 없음
Description
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음
Claims (16)
- 유액전체 중량에 대하여, a) 퍼플루오로폴리에테르 0.01중량%∼99.9중량%, b) 표면활성제 0.01중량%∼30중량%, 및 c) 글리세롤 100중량%이하로 구성됨을 특징으로하는, 피플루오로알킬 말단기를 갖는 퍼플루오로폴리에테르 안정유액.
- 유액 전체 중량에 대하여, a) 퍼플루오로폴리에테르 0.01중량%∼80중량%, b) 표면활성제 0.01중량%∼30중량%, 및 c) 3개 이상의 히드록실기를 함유하는 다가 알콜 및 당류로 부터 선택된 폴리히드록실화 화합물을 친수성 용매에 용해시킨 용액 100중량%이하로 구성됨을 특징으로하는, 퍼플루오로알킬 말단기를 갖는 퍼플루오로오로폴리에테르 안정유액.
- 제1항에 있어서, 유액 전체중량에 대하여, a) 피플루오로폴리에테르 0.1중량%∼75중량%, b) 표면활성제 0.01중량%∼5중량%, 및 c) 글리세롤 100중량%이하로 구성됨을 특징으로하는 유액.
- 제2항에 있어서, 유액전체 중량에 대하여, a) 피플루오로폴리에테르 0.01중량%∼50중량%, b) 표면활성제 0.01중량%∼5중량%, 및 c) 3개 이상의 히드록실기를 함유하는 다가 알콜 및 당류로 부터 선택된 플리히드록실 화합물을 친수성 용매에 용해시킨 용액 100중량%이하로 구성됨을 특징으로하는 용액.
- 제1 내지 4항중 어느 한항에 있어서, 피플루오로폴리에테르가 하기의 피플루오로옥시알킬렌 반복단위를 하나 이상 함유하는 퍼플루오로폴리에테르류로 부터 선택된 유액.[상기식중, 기Rf'''는 서로 동일 또는 상이하며, 불소 원자 또는 피플루오로알킬기이다].
- 제1 내지 5항중 어느 한 항에 있어서, 피플루오로폴리에테르가 단일종 또는 서로 조합된 하기의 피플루오로옥시알킬렌 단위를 함유하는 것들로 부터 선택된 유액. I) (CF2-CF2O) 및 (CF2O) 상기 단위는 피플루오로폴리에테르 사슬을 따라서 통계상 분포됨 또는 II)및 (CFXO) (여기서 X는 F 또는 CF3이다). 상기 단위는 사슬을 따라서 통계상 분포됨 또는 III) (CF2-CF2O),및 (CFXO) (여기서, X는 F 또는 F3이다). 상기 단위는 사슬을 따라서 통계상 분포됨, 또는 IV)또는 V) (CF2-CF2-CF2O) 또는 VI) (CF2-CF2O) 또는 VII)[상기식중, 기Rf'''는 서로 동일 또는 상이하며, 불소 원자 또는 피플루오로알킬기이다). 또는 VIII) (CF2O-CF2-CF2O)
- 제1 내지 6항중 어느 한 항에 있어서, 피플루오로폴리에테르가 하기 일반식의 피플로오로옥세탄 고리를 함유하는 것들로 부터 선택된 유액;[상기식중, T,B 및 R은 서로 동일 또는 상이하며, 퍼플루오로옥시알킬, 퍼플루오로폴리옥시알킬 또는 퍼플루오로아릴 라디칼이고, A는 피플루오로옥시알키, 퍼플루오로폴리옥시알킬 또는 퍼플루로알킬 라디칼이다].
- 제1 내지 7항중 어느 한 항에 있어서, 퍼플루오로 폴리에테르가 하기 부류에 속하는 것들로 부터 선택된 유액;[상기식중, Rf'는 서로 동일 또는 상이하며, CF3, C2F3및 C3F7으로 구성된 군으로부터 선택되고, 단위 C3F6O(옥시트리플루오로메틸트리플루오로 에틸렌),및 CF2-O는 사슬을 따라서 통계상 분포되며, a는 정수이고, b와 c는 정수 또는 0인데, 합계(b+c)가 0이 아닐 경우에비는 5∼40범위이다;B) CF3O-(C2F4O)d(CF2O)e-CF3[상기식 중, 단위 C2F4O 및 CF2O는 사슬을 따라서 통계상 분포되고, d와 e는 정수인데, d/e 비는 0.3∼5범위이다];C) CF3O-(C3F6O)f(C2F4O)g(CFXO)|h-CF3[상기식 중, 단위 C3F6O, C2F4O 및 CFXO는 사실을 따라서 통계상 분포되고; X는 F 또는 CF3이며, f, g 및 h는 정수인데;비는 1∼50범위이고;비는 1∼10 범위이다];D) R3 fO-(CF2CF2CF2O)jR4 f[상기식 중, R3 f및 R4 f서로 동일 또는 상이하며, -CF3또는 -C2F5이고, j는 정수이다].
- 제1 내지 8항중 어느 한 항에 있어서, 퍼플루오로 플리에테르의 수평균 분자량이 500∼20,000범위인 유액.
- 제1 내지 9항중 어느 한 항에 있어서, 퍼플루오로 폴리에테르의 수평균 분자량이 1,000∼10,000 범위인 유액.
- 제1 내지 10항중 어느 한 항에 있어서, 3∼12의 탄소수를 함유하는 4다가 알콜과 4∼18의 탄소수를 함유하는 당류 및 다당류의 가수분해물의 혼합물로 부터 선택된 플리히드록실화 화합물을 친수성 용매에 용해시킨 용액을 사용한 유액.
- 제1 내지 11항중 어느 한 항에 있어서, 글리콜류, 글리세롤, 저급 알콜류, 에테르류, 더글림류 및 물 또는 이들의 혼합물로 부터 선택된 친수성 용매가 사용된 유액.
- 제1 내지 12항중 어느 한항에 있어서, 크실리톨, 만니톨, 소르비톨, 글루코오스, 말리틀, 사카로오스, 프룩토오스, 디글리세롤, 트리글리세롤, 테트라글리세롤부터 선택된 폴리히드록실화 화합물의 농축 용액을 사용한 유액.
- 제1 내지 13항중 어느 한항에 있어서, 사용된 용액이 친수성 용매중에서 50∼80중량의 폴리히드록실화 화합물농도를 갖는 유액.
- 제1 내지 14항중 어느 한 항에 있어서, 유화제가 양이온성, 음이온성, 양쪽성 및 비이온성 유화제로 부터 선택된 유액.
- 제1 내지 15항중 어느 한 항에 따른 퍼플루오로알킬 말단기를 갖는 퍼플루오로 폴리에테르 유액을 함유하는 피부 미용 조성물.※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
IT199744A/89 | 1989-03-21 | ||
IT19974A/89 | 1989-03-31 | ||
IT8919974A IT1229222B (it) | 1989-03-31 | 1989-03-31 | Emulsioni stabili di perfluoropolieteri |
Publications (2)
Publication Number | Publication Date |
---|---|
KR900013941A true KR900013941A (ko) | 1990-10-22 |
KR0146054B1 KR0146054B1 (ko) | 1998-08-17 |
Family
ID=11162770
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR1019900004411A KR0146054B1 (ko) | 1989-03-31 | 1990-03-31 | 퍼플루오로폴리에테르 안정유액 |
Country Status (10)
Country | Link |
---|---|
US (3) | US5183589A (ko) |
EP (1) | EP0390206B1 (ko) |
JP (1) | JP2880239B2 (ko) |
KR (1) | KR0146054B1 (ko) |
AT (1) | ATE143033T1 (ko) |
AU (1) | AU624491B2 (ko) |
DE (1) | DE69028564T2 (ko) |
ES (1) | ES2094126T3 (ko) |
IT (1) | IT1229222B (ko) |
ZA (1) | ZA902443B (ko) |
Families Citing this family (75)
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FR2675377B1 (fr) * | 1991-04-22 | 1995-02-03 | Oreal | Microspheres poreuses enrobees a l'aide d'une huile perfluoree, d'une huile de silicone fluoree ou d'une gomme de silicone et leur utilisation en cosmetique. |
GB9109693D0 (en) * | 1991-05-03 | 1991-06-26 | Unilever Plc | Hair treatment composition |
FR2687932A1 (fr) * | 1992-02-27 | 1993-09-03 | Oreal | Dispersion huile-dans-l'eau susceptible de former des films composites. |
FR2688006A1 (fr) * | 1992-02-27 | 1993-09-03 | Oreal | Dispersion d'un hydrocarbure fluore dans une solution aqueuse d'un polymere filmogene et son utilisation pour la formation de films composites notamment en cosmetique. |
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FR2700691B1 (fr) * | 1993-01-25 | 1995-04-07 | Oreal | Composition homogène à base de composés fluorés et de glycols, procédé de préparation et utilisation en cosmétique. |
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-
1989
- 1989-03-31 IT IT8919974A patent/IT1229222B/it active
-
1990
- 1990-03-29 ZA ZA902443A patent/ZA902443B/xx unknown
- 1990-03-30 AT AT90106181T patent/ATE143033T1/de not_active IP Right Cessation
- 1990-03-30 US US07/501,481 patent/US5183589A/en not_active Expired - Fee Related
- 1990-03-30 EP EP90106181A patent/EP0390206B1/en not_active Expired - Lifetime
- 1990-03-30 AU AU52473/90A patent/AU624491B2/en not_active Ceased
- 1990-03-30 DE DE69028564T patent/DE69028564T2/de not_active Expired - Fee Related
- 1990-03-30 ES ES90106181T patent/ES2094126T3/es not_active Expired - Lifetime
- 1990-03-31 JP JP2087338A patent/JP2880239B2/ja not_active Expired - Fee Related
- 1990-03-31 KR KR1019900004411A patent/KR0146054B1/ko not_active IP Right Cessation
-
1992
- 1992-09-29 US US07/953,128 patent/US5330681A/en not_active Expired - Lifetime
-
1994
- 1994-06-06 US US08/254,778 patent/US5562911A/en not_active Expired - Lifetime
Also Published As
Publication number | Publication date |
---|---|
EP0390206A2 (en) | 1990-10-03 |
KR0146054B1 (ko) | 1998-08-17 |
JP2880239B2 (ja) | 1999-04-05 |
JPH0395262A (ja) | 1991-04-19 |
DE69028564D1 (de) | 1996-10-24 |
ATE143033T1 (de) | 1996-10-15 |
US5183589A (en) | 1993-02-02 |
EP0390206B1 (en) | 1996-09-18 |
ZA902443B (en) | 1991-01-30 |
EP0390206A3 (en) | 1991-06-26 |
ES2094126T3 (es) | 1997-01-16 |
IT8919974A0 (it) | 1989-03-31 |
DE69028564T2 (de) | 1997-01-30 |
IT1229222B (it) | 1991-07-26 |
US5330681A (en) | 1994-07-19 |
US5562911A (en) | 1996-10-08 |
AU624491B2 (en) | 1992-06-11 |
AU5247390A (en) | 1990-10-04 |
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