JP3939761B2 - 着色スルホポリエステルを含む水性リップグロス及び化粧料組成物 - Google Patents
着色スルホポリエステルを含む水性リップグロス及び化粧料組成物 Download PDFInfo
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- JP3939761B2 JP3939761B2 JP54273797A JP54273797A JP3939761B2 JP 3939761 B2 JP3939761 B2 JP 3939761B2 JP 54273797 A JP54273797 A JP 54273797A JP 54273797 A JP54273797 A JP 54273797A JP 3939761 B2 JP3939761 B2 JP 3939761B2
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- acid
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- hydroxy
- cosmetic composition
- sulfopolyester
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- 239000000203 mixture Substances 0.000 title claims description 49
- 239000002537 cosmetic Substances 0.000 title claims description 35
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- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims description 14
- 150000002009 diols Chemical class 0.000 claims description 13
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- 125000004356 hydroxy functional group Chemical group O* 0.000 claims description 11
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 10
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- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 8
- 125000001424 substituent group Chemical group 0.000 claims description 7
- YIMQCDZDWXUDCA-UHFFFAOYSA-N [4-(hydroxymethyl)cyclohexyl]methanol Chemical compound OCC1CCC(CO)CC1 YIMQCDZDWXUDCA-UHFFFAOYSA-N 0.000 claims description 6
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- 238000004458 analytical method Methods 0.000 description 3
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- 125000005708 carbonyloxy group Chemical group [*:2]OC([*:1])=O 0.000 description 3
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- 229910052736 halogen Inorganic materials 0.000 description 3
- 150000002367 halogens Chemical class 0.000 description 3
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- PEGWTYUTVJVAJO-UHFFFAOYSA-N 1,5-bis[(3-hydroxy-2,2-dimethylpropyl)amino]anthracene-9,10-dione Chemical compound O=C1C2=C(NCC(C)(C)CO)C=CC=C2C(=O)C2=C1C=CC=C2NCC(C)(CO)C PEGWTYUTVJVAJO-UHFFFAOYSA-N 0.000 description 2
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- LCKIEQZJEYYRIY-UHFFFAOYSA-N Titanium ion Chemical compound [Ti+4] LCKIEQZJEYYRIY-UHFFFAOYSA-N 0.000 description 1
- AHWXCYJGJOLNFA-UHFFFAOYSA-N [1,4]benzoxazino[2,3-b]phenoxazine Chemical compound O1C2=CC=CC=C2N=C2C1=CC1=NC3=CC=CC=C3OC1=C2 AHWXCYJGJOLNFA-UHFFFAOYSA-N 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- CTSKAPUYEZZYQA-UHFFFAOYSA-N ac1lgnjz Chemical compound C1=CC(C(=O)C=2C3=CC=CC=2)=C2C3=CC(=O)NC2=C1 CTSKAPUYEZZYQA-UHFFFAOYSA-N 0.000 description 1
- 150000008065 acid anhydrides Chemical class 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 159000000032 aromatic acids Chemical class 0.000 description 1
- 235000013871 bee wax Nutrition 0.000 description 1
- 239000012166 beeswax Substances 0.000 description 1
- 229940092738 beeswax Drugs 0.000 description 1
- 239000000440 bentonite Substances 0.000 description 1
- 229910000278 bentonite Inorganic materials 0.000 description 1
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 1
- LXARMRGJFVAFPR-UHFFFAOYSA-N benzo[a]phenoxazin-5-one Chemical compound C12=CC=CC=C2C(=O)C=C2C1=NC1=CC=CC=C1O2 LXARMRGJFVAFPR-UHFFFAOYSA-N 0.000 description 1
- WWXLKPRGAXWHFO-UHFFFAOYSA-N benzo[e]perimidin-7-one Chemical compound C1=CC(C(=O)C=2C3=CC=CC=2)=C2C3=NC=NC2=C1 WWXLKPRGAXWHFO-UHFFFAOYSA-N 0.000 description 1
- 235000010290 biphenyl Nutrition 0.000 description 1
- 239000004305 biphenyl Substances 0.000 description 1
- 125000006267 biphenyl group Chemical group 0.000 description 1
- 229940073609 bismuth oxychloride Drugs 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- DBZJJPROPLPMSN-UHFFFAOYSA-N bromoeosin Chemical compound O1C(=O)C2=CC=CC=C2C21C1=CC(Br)=C(O)C(Br)=C1OC1=C(Br)C(O)=C(Br)C=C21 DBZJJPROPLPMSN-UHFFFAOYSA-N 0.000 description 1
- 239000000872 buffer Substances 0.000 description 1
- KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 description 1
- 239000004204 candelilla wax Substances 0.000 description 1
- 235000013868 candelilla wax Nutrition 0.000 description 1
- 229940073532 candelilla wax Drugs 0.000 description 1
- 150000001720 carbohydrates Chemical class 0.000 description 1
- 235000014633 carbohydrates Nutrition 0.000 description 1
- 239000004203 carnauba wax Substances 0.000 description 1
- 235000013869 carnauba wax Nutrition 0.000 description 1
- 229940082483 carnauba wax Drugs 0.000 description 1
- 229960001777 castor oil Drugs 0.000 description 1
- 150000001768 cations Chemical class 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 229960000541 cetyl alcohol Drugs 0.000 description 1
- 239000002738 chelating agent Substances 0.000 description 1
- 150000001805 chlorine compounds Chemical class 0.000 description 1
- OACTWOBLPKAISB-UHFFFAOYSA-N chromen-2-one Chemical compound C1=CC=C2OC(=O)C=CC2=C1.C1=CC=C2OC(=O)C=CC2=C1 OACTWOBLPKAISB-UHFFFAOYSA-N 0.000 description 1
- 239000000084 colloidal system Substances 0.000 description 1
- 235000005687 corn oil Nutrition 0.000 description 1
- 239000002285 corn oil Substances 0.000 description 1
- 239000006184 cosolvent Substances 0.000 description 1
- 239000006071 cream Substances 0.000 description 1
- 125000004093 cyano group Chemical group *C#N 0.000 description 1
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
- RAABOESOVLLHRU-UHFFFAOYSA-N diazene Chemical compound N=N RAABOESOVLLHRU-UHFFFAOYSA-N 0.000 description 1
- 229910000071 diazene Inorganic materials 0.000 description 1
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N dimethylmethane Natural products CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 1
- USIUVYZYUHIAEV-UHFFFAOYSA-N diphenyl ether Chemical group C=1C=CC=CC=1OC1=CC=CC=C1 USIUVYZYUHIAEV-UHFFFAOYSA-N 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 229960001483 eosin Drugs 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 150000002191 fatty alcohols Chemical class 0.000 description 1
- 239000008394 flocculating agent Substances 0.000 description 1
- 239000007850 fluorescent dye Substances 0.000 description 1
- FBPFZTCFMRRESA-GUCUJZIJSA-N galactitol Chemical compound OC[C@H](O)[C@@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-GUCUJZIJSA-N 0.000 description 1
- 235000013922 glutamic acid Nutrition 0.000 description 1
- 239000004220 glutamic acid Substances 0.000 description 1
- 150000002314 glycerols Chemical class 0.000 description 1
- IUJAMGNYPWYUPM-UHFFFAOYSA-N hentriacontane Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC IUJAMGNYPWYUPM-UHFFFAOYSA-N 0.000 description 1
- XXMIOPMDWAUFGU-UHFFFAOYSA-N hexane-1,6-diol Chemical compound OCCCCCCO XXMIOPMDWAUFGU-UHFFFAOYSA-N 0.000 description 1
- 125000004464 hydroxyphenyl group Chemical group 0.000 description 1
- 239000006115 industrial coating Substances 0.000 description 1
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
- 229940119170 jojoba wax Drugs 0.000 description 1
- 239000000787 lecithin Substances 0.000 description 1
- 235000010445 lecithin Nutrition 0.000 description 1
- 229940067606 lecithin Drugs 0.000 description 1
- 125000005647 linker group Chemical group 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000006210 lotion Substances 0.000 description 1
- 125000000040 m-tolyl group Chemical group [H]C1=C([H])C(*)=C([H])C(=C1[H])C([H])([H])[H] 0.000 description 1
- 239000000594 mannitol Substances 0.000 description 1
- 235000010355 mannitol Nutrition 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- GOQYKNQRPGWPLP-UHFFFAOYSA-N n-heptadecyl alcohol Natural products CCCCCCCCCCCCCCCCCO GOQYKNQRPGWPLP-UHFFFAOYSA-N 0.000 description 1
- AWIZFKXFPHTRHN-UHFFFAOYSA-N naphtho[2,3-f]quinoline Chemical compound C1=CC=C2C3=CC4=CC=CC=C4C=C3C=CC2=N1 AWIZFKXFPHTRHN-UHFFFAOYSA-N 0.000 description 1
- 229940049964 oleate Drugs 0.000 description 1
- 229940055577 oleyl alcohol Drugs 0.000 description 1
- XMLQWXUVTXCDDL-UHFFFAOYSA-N oleyl alcohol Natural products CCCCCCC=CCCCCCCCCCCO XMLQWXUVTXCDDL-UHFFFAOYSA-N 0.000 description 1
- 239000003605 opacifier Substances 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 239000011368 organic material Substances 0.000 description 1
- BWOROQSFKKODDR-UHFFFAOYSA-N oxobismuth;hydrochloride Chemical compound Cl.[Bi]=O BWOROQSFKKODDR-UHFFFAOYSA-N 0.000 description 1
- 125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 description 1
- 125000001037 p-tolyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])([H])[H] 0.000 description 1
- 239000005022 packaging material Substances 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 239000002304 perfume Substances 0.000 description 1
- DGBWPZSGHAXYGK-UHFFFAOYSA-N perinone Chemical compound C12=NC3=CC=CC=C3N2C(=O)C2=CC=C3C4=C2C1=CC=C4C(=O)N1C2=CC=CC=C2N=C13 DGBWPZSGHAXYGK-UHFFFAOYSA-N 0.000 description 1
- 125000002080 perylenyl group Chemical group C1(=CC=C2C=CC=C3C4=CC=CC5=CC=CC(C1=C23)=C45)* 0.000 description 1
- CSHWQDPOILHKBI-UHFFFAOYSA-N peryrene Natural products C1=CC(C2=CC=CC=3C2=C2C=CC=3)=C3C2=CC=CC3=C1 CSHWQDPOILHKBI-UHFFFAOYSA-N 0.000 description 1
- 229940066842 petrolatum Drugs 0.000 description 1
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 1
- 150000003904 phospholipids Chemical class 0.000 description 1
- 229920006122 polyamide resin Polymers 0.000 description 1
- 229920001083 polybutene Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920006149 polyester-amide block copolymer Polymers 0.000 description 1
- 229940113115 polyethylene glycol 200 Drugs 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- PBYUNDCGVVYTIG-UHFFFAOYSA-N propane-1,2-diol;tetradecyl acetate Chemical compound CC(O)CO.CCCCCCCCCCCCCCOC(C)=O PBYUNDCGVVYTIG-UHFFFAOYSA-N 0.000 description 1
- IZMJMCDDWKSTTK-UHFFFAOYSA-N quinoline yellow Chemical compound C1=CC=CC2=NC(C3C(C4=CC=CC=C4C3=O)=O)=CC=C21 IZMJMCDDWKSTTK-UHFFFAOYSA-N 0.000 description 1
- 239000001044 red dye Substances 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000012177 spermaceti Substances 0.000 description 1
- 229940084106 spermaceti Drugs 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- 125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
- 150000000000 tetracarboxylic acids Chemical class 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- YRHRIQCWCFGUEQ-UHFFFAOYSA-N thioxanthen-9-one Chemical compound C1=CC=C2C(=O)C3=CC=CC=C3SC2=C1 YRHRIQCWCFGUEQ-UHFFFAOYSA-N 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 1
- 239000000080 wetting agent Substances 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
- A61K8/84—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
- A61K8/85—Polyesters
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q1/00—Make-up preparations; Body powders; Preparations for removing make-up
- A61Q1/02—Preparations containing skin colorants, e.g. pigments
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q1/00—Make-up preparations; Body powders; Preparations for removing make-up
- A61Q1/02—Preparations containing skin colorants, e.g. pigments
- A61Q1/04—Preparations containing skin colorants, e.g. pigments for lips
-
- 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
- A61K2800/57—Compounds covalently linked to a(n inert) carrier molecule, e.g. conjugates, pro-fragrances
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)
- Cosmetics (AREA)
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US1781296P | 1996-05-28 | 1996-05-28 | |
| US60/017,812 | 1996-10-10 | ||
| US08/728,455 US5744129A (en) | 1996-05-28 | 1996-10-10 | Aqueous lip gloss and cosmetic compositions containing colored sulfopolyesters |
| US08/728,455 | 1996-10-10 | ||
| PCT/US1997/008719 WO1997045094A1 (en) | 1996-05-28 | 1997-05-16 | Aqueous lip gloss and cosmetic compositions containing colored sulfopolyesters |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2000511185A JP2000511185A (ja) | 2000-08-29 |
| JP2000511185A5 JP2000511185A5 (Direct) | 2004-12-09 |
| JP3939761B2 true JP3939761B2 (ja) | 2007-07-04 |
Family
ID=26690351
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP54273797A Expired - Fee Related JP3939761B2 (ja) | 1996-05-28 | 1997-05-16 | 着色スルホポリエステルを含む水性リップグロス及び化粧料組成物 |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US5744129A (Direct) |
| EP (1) | EP0906079B1 (Direct) |
| JP (1) | JP3939761B2 (Direct) |
| BR (1) | BR9709383A (Direct) |
| DE (1) | DE69703737D1 (Direct) |
| WO (1) | WO1997045094A1 (Direct) |
Families Citing this family (22)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2757048B1 (fr) * | 1996-12-16 | 1999-08-27 | Oreal | Composition cosmetique sous la forme d'une dispersion aqueuse comprenant au moins un colorant polymerique |
| FR2760642B1 (fr) * | 1997-03-14 | 2002-11-22 | Oreal | Composition topique comprenant un gelifiant hydrophile de type polyester sulfone |
| FR2783161B1 (fr) * | 1998-09-11 | 2000-10-13 | Oreal | Composition aqueuse comprenant un melange de polyesters sulfones |
| FR2783160A1 (fr) | 1998-09-14 | 2000-03-17 | Oreal | Composition cosmetique aqueuse comprenant un polyester sulfone et un compose silicone |
| FR2794021A1 (fr) * | 1999-04-28 | 2000-12-01 | Oreal | Utilisation d'un sulfopolyester colorant pour obtenir un film resistant aux frottements |
| FR2792829B1 (fr) * | 1999-04-28 | 2004-02-13 | Oreal | Composition cosmetique comprenant une microdispersion de cire et un polymere colorant |
| EP1475071B1 (de) * | 2003-05-09 | 2008-02-27 | Basf Aktiengesellschaft | Kosmetische Zusammensetzungen enthaltend Cyclohexanpolycarbonsäurederivate |
| US8363951B2 (en) * | 2007-03-05 | 2013-01-29 | DigitalOptics Corporation Europe Limited | Face recognition training method and apparatus |
| US8553949B2 (en) * | 2004-01-22 | 2013-10-08 | DigitalOptics Corporation Europe Limited | Classification and organization of consumer digital images using workflow, and face detection and recognition |
| US8189927B2 (en) | 2007-03-05 | 2012-05-29 | DigitalOptics Corporation Europe Limited | Face categorization and annotation of a mobile phone contact list |
| US7564994B1 (en) * | 2004-01-22 | 2009-07-21 | Fotonation Vision Limited | Classification system for consumer digital images using automatic workflow and face detection and recognition |
| DE102004029732A1 (de) * | 2004-06-21 | 2006-01-19 | Basf Ag | Hilfsmittel enthaltend Cyclohexanpolycarbonsäurederivate |
| US7715597B2 (en) * | 2004-12-29 | 2010-05-11 | Fotonation Ireland Limited | Method and component for image recognition |
| US20100008880A1 (en) * | 2006-05-03 | 2010-01-14 | John Castro | Clear Cosmetic Compositions And Methods Of Using |
| US20070259012A1 (en) * | 2006-05-03 | 2007-11-08 | John Castro | Clear Cosmetic Compositions and Methods Of Use |
| EP2050043A2 (en) * | 2006-08-02 | 2009-04-22 | Fotonation Vision Limited | Face recognition with combined pca-based datasets |
| US8236289B2 (en) * | 2007-06-15 | 2012-08-07 | Coty S.A.S. | Lip gloss |
| US20090047229A1 (en) * | 2007-06-15 | 2009-02-19 | Coty S.A.S | Lip gloss |
| WO2010063463A2 (en) * | 2008-12-05 | 2010-06-10 | Fotonation Ireland Limited | Face recognition using face tracker classifier data |
| US8778316B2 (en) * | 2008-12-11 | 2014-07-15 | L'oreal | Non-sticky, hydrating and moisturizing aqueous lip gloss composition |
| US20100158821A1 (en) * | 2008-12-22 | 2010-06-24 | Eastman Chemical Company | Antimicrobial agents, compositions and products containing the same, and methods of using the compositions and products |
| US8106111B2 (en) * | 2009-05-15 | 2012-01-31 | Eastman Chemical Company | Antimicrobial effect of cycloaliphatic diol antimicrobial agents in coating compositions |
Family Cites Families (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3148125A (en) * | 1961-03-22 | 1964-09-08 | Yardley Of London Inc | Clear lipstick |
| US3546008A (en) * | 1968-01-03 | 1970-12-08 | Eastman Kodak Co | Sizing compositions and fibrous articles sized therewith |
| US3779993A (en) * | 1970-02-27 | 1973-12-18 | Eastman Kodak Co | Polyesters and polyesteramides containing ether groups and sulfonate groups in the form of a metallic salt |
| US3734874A (en) * | 1970-02-27 | 1973-05-22 | Eastman Kodak Co | Polyesters and polyesteramides containing ether groups and sulfonate groups in the form of a metallic salt |
| US3957969A (en) * | 1973-07-13 | 1976-05-18 | Shiseeido Co., Ltd. | Cosmetic stick comprising water-in-oil emulsion |
| US4279662A (en) * | 1976-12-17 | 1981-07-21 | Dynapol | Polymeric red colors |
| US4233196A (en) * | 1979-04-30 | 1980-11-11 | Eastman Kodak Company | Polyester and polyesteramide compositions |
| US4335220A (en) * | 1981-04-06 | 1982-06-15 | Eastman Kodak Company | Sequestering agents and compositions produced therefrom |
| FR2514639B1 (fr) * | 1981-10-15 | 1986-08-01 | Oreal | Compositions cosmetiques pour le maquillage contenant en tant que pigments colores un sel d'un colorant acide et d'un polymere porteur de fonctions amines salifiees ou quaternisees |
| US4804719A (en) * | 1988-02-05 | 1989-02-14 | Eastman Kodak Company | Water-dissipatable polyester and polyester-amides containing copolymerized colorants |
| US5143723A (en) * | 1988-11-23 | 1992-09-01 | Estee Lauder, Inc. | Colored cosmetic compositions |
| US5055500A (en) * | 1989-10-24 | 1991-10-08 | Eastman Kodak Company | Process for treating pigments |
| US5085856A (en) * | 1990-07-25 | 1992-02-04 | Elizabeth Arden Co., Division Of Conopco, Inc. | Cosmetic water-in-oil emulsion lipstick comprising a phospholipid and glycerol fatty acid esters emulsifying system |
| US5266322A (en) * | 1992-05-29 | 1993-11-30 | Eastman Kodak Company | Cosmetic film forming compositions |
-
1996
- 1996-10-10 US US08/728,455 patent/US5744129A/en not_active Expired - Lifetime
-
1997
- 1997-05-16 DE DE69703737T patent/DE69703737D1/de not_active Expired - Lifetime
- 1997-05-16 JP JP54273797A patent/JP3939761B2/ja not_active Expired - Fee Related
- 1997-05-16 EP EP97925704A patent/EP0906079B1/en not_active Expired - Lifetime
- 1997-05-16 WO PCT/US1997/008719 patent/WO1997045094A1/en not_active Ceased
- 1997-05-16 BR BR9709383A patent/BR9709383A/pt not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| EP0906079B1 (en) | 2000-12-20 |
| US5744129A (en) | 1998-04-28 |
| WO1997045094A1 (en) | 1997-12-04 |
| EP0906079A1 (en) | 1999-04-07 |
| DE69703737D1 (de) | 2001-01-25 |
| BR9709383A (pt) | 1999-08-10 |
| JP2000511185A (ja) | 2000-08-29 |
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