MXPA97001609A - Composition threatened by a polisacar alquileter - Google Patents
Composition threatened by a polisacar alquileterInfo
- Publication number
- MXPA97001609A MXPA97001609A MXPA/A/1997/001609A MX9701609A MXPA97001609A MX PA97001609 A MXPA97001609 A MX PA97001609A MX 9701609 A MX9701609 A MX 9701609A MX PA97001609 A MXPA97001609 A MX PA97001609A
- Authority
- MX
- Mexico
- Prior art keywords
- composition according
- alkyl ether
- composition
- gum
- polysaccharide
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 70
- -1 polysaccharide alkyl ether Chemical class 0.000 claims abstract description 20
- 239000002537 cosmetic Substances 0.000 claims abstract description 16
- 229920001282 polysaccharide Polymers 0.000 claims abstract description 16
- 239000005017 polysaccharide Substances 0.000 claims abstract description 16
- 239000002562 thickening agent Substances 0.000 claims abstract description 15
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 12
- 229930195734 saturated hydrocarbon Natural products 0.000 claims abstract description 10
- 150000005215 alkyl ethers Chemical class 0.000 claims abstract description 7
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims abstract description 7
- 238000006467 substitution reaction Methods 0.000 claims abstract description 7
- 239000003921 oil Substances 0.000 claims description 18
- 239000000126 substance Substances 0.000 claims description 9
- 125000004432 carbon atom Chemical group C* 0.000 claims description 8
- 229930182830 galactose Natural products 0.000 claims description 6
- 239000001993 wax Substances 0.000 claims description 6
- 229920002907 Guar gum Polymers 0.000 claims description 5
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 5
- 239000000665 guar gum Substances 0.000 claims description 5
- 235000010417 guar gum Nutrition 0.000 claims description 5
- 229960002154 guar gum Drugs 0.000 claims description 5
- 239000004615 ingredient Substances 0.000 claims description 5
- 239000002674 ointment Substances 0.000 claims description 5
- 239000000049 pigment Substances 0.000 claims description 5
- WQZGKKKJIJFFOK-PHYPRBDBSA-N alpha-D-galactose Chemical compound OC[C@H]1O[C@H](O)[C@H](O)[C@@H](O)[C@H]1O WQZGKKKJIJFFOK-PHYPRBDBSA-N 0.000 claims description 4
- 239000002304 perfume Substances 0.000 claims description 4
- 239000003755 preservative agent Substances 0.000 claims description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 4
- SHZGCJCMOBCMKK-UHFFFAOYSA-N D-mannomethylose Natural products CC1OC(O)C(O)C(O)C1O SHZGCJCMOBCMKK-UHFFFAOYSA-N 0.000 claims description 3
- WQZGKKKJIJFFOK-QTVWNMPRSA-N D-mannopyranose Chemical compound OC[C@H]1OC(O)[C@@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-QTVWNMPRSA-N 0.000 claims description 3
- SHZGCJCMOBCMKK-JFNONXLTSA-N L-rhamnopyranose Chemical compound C[C@@H]1OC(O)[C@H](O)[C@H](O)[C@H]1O SHZGCJCMOBCMKK-JFNONXLTSA-N 0.000 claims description 3
- PNNNRSAQSRJVSB-UHFFFAOYSA-N L-rhamnose Natural products CC(O)C(O)C(O)C(O)C=O PNNNRSAQSRJVSB-UHFFFAOYSA-N 0.000 claims description 3
- 229920000161 Locust bean gum Polymers 0.000 claims description 3
- PYMYPHUHKUWMLA-WDCZJNDASA-N arabinose Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)C=O PYMYPHUHKUWMLA-WDCZJNDASA-N 0.000 claims description 3
- PYMYPHUHKUWMLA-UHFFFAOYSA-N arabinose Natural products OCC(O)C(O)C(O)C=O PYMYPHUHKUWMLA-UHFFFAOYSA-N 0.000 claims description 3
- SRBFZHDQGSBBOR-UHFFFAOYSA-N beta-D-Pyranose-Lyxose Natural products OC1COC(O)C(O)C1O SRBFZHDQGSBBOR-UHFFFAOYSA-N 0.000 claims description 3
- 230000015572 biosynthetic process Effects 0.000 claims description 3
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 3
- 239000006185 dispersion Substances 0.000 claims description 3
- 239000000194 fatty acid Substances 0.000 claims description 3
- 229930195729 fatty acid Natural products 0.000 claims description 3
- 239000000711 locust bean gum Substances 0.000 claims description 3
- 235000010420 locust bean gum Nutrition 0.000 claims description 3
- 238000000034 method Methods 0.000 claims description 3
- NRTKYSGFUISGRQ-UHFFFAOYSA-N (3-heptanoyloxy-2,2-dimethylpropyl) heptanoate Chemical compound CCCCCCC(=O)OCC(C)(C)COC(=O)CCCCCC NRTKYSGFUISGRQ-UHFFFAOYSA-N 0.000 claims description 2
- ALSTYHKOOCGGFT-KTKRTIGZSA-N (9Z)-octadecen-1-ol Chemical compound CCCCCCCC\C=C/CCCCCCCCO ALSTYHKOOCGGFT-KTKRTIGZSA-N 0.000 claims description 2
- OVYMWJFNQQOJBU-UHFFFAOYSA-N 1-octanoyloxypropan-2-yl octanoate Chemical compound CCCCCCCC(=O)OCC(C)OC(=O)CCCCCCC OVYMWJFNQQOJBU-UHFFFAOYSA-N 0.000 claims description 2
- FWIUBOWVXREPPL-UHFFFAOYSA-N 2-[2-(7-methyloctanoyloxy)ethoxy]ethyl 7-methyloctanoate Chemical compound CC(C)CCCCCC(=O)OCCOCCOC(=O)CCCCCC(C)C FWIUBOWVXREPPL-UHFFFAOYSA-N 0.000 claims description 2
- 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 description 2
- 239000013543 active substance Substances 0.000 claims description 2
- 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 description 2
- HGKOWIQVWAQWDS-UHFFFAOYSA-N bis(16-methylheptadecyl) 2-hydroxybutanedioate Chemical compound CC(C)CCCCCCCCCCCCCCCOC(=O)CC(O)C(=O)OCCCCCCCCCCCCCCCC(C)C HGKOWIQVWAQWDS-UHFFFAOYSA-N 0.000 claims description 2
- ALSTYHKOOCGGFT-UHFFFAOYSA-N cis-oleyl alcohol Natural products CCCCCCCCC=CCCCCCCCCO ALSTYHKOOCGGFT-UHFFFAOYSA-N 0.000 claims description 2
- 150000002243 furanoses Chemical class 0.000 claims description 2
- 239000008103 glucose Substances 0.000 claims description 2
- LTYSCLBTUYRCBF-UHFFFAOYSA-N icosan-9-yl 2-hydroxyoctadecanoate Chemical compound CCCCCCCCCCCCCCCCC(O)C(=O)OC(CCCCCCCC)CCCCCCCCCCC LTYSCLBTUYRCBF-UHFFFAOYSA-N 0.000 claims description 2
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 claims description 2
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 2
- 239000007934 lip balm Substances 0.000 claims description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 2
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 2
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 2
- 239000007764 o/w emulsion Substances 0.000 claims description 2
- 238000002360 preparation method Methods 0.000 claims description 2
- 238000003786 synthesis reaction Methods 0.000 claims description 2
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 2
- COXJMKGEQAWXNP-UHFFFAOYSA-N tris(14-methylpentadecyl) 2-hydroxypropane-1,2,3-tricarboxylate Chemical compound CC(C)CCCCCCCCCCCCCOC(=O)CC(O)(C(=O)OCCCCCCCCCCCCCC(C)C)CC(=O)OCCCCCCCCCCCCCC(C)C COXJMKGEQAWXNP-UHFFFAOYSA-N 0.000 claims description 2
- 229920000569 Gum karaya Polymers 0.000 claims 2
- 241000934878 Sterculia Species 0.000 claims 2
- 239000000231 karaya gum Substances 0.000 claims 2
- 235000010494 karaya gum Nutrition 0.000 claims 2
- 229940039371 karaya gum Drugs 0.000 claims 2
- GCFJQIPKMMUXCU-UHFFFAOYSA-N OC(C(=O)OCCCCCCCC)CCCCCCCCCCCCCCCC.C(C(O)C)(=O)OCCCCCCCCCCCCCCCC(C)C Chemical compound OC(C(=O)OCCCCCCCC)CCCCCCCCCCCCCCCC.C(C(O)C)(=O)OCCCCCCCCCCCCCCCC(C)C GCFJQIPKMMUXCU-UHFFFAOYSA-N 0.000 claims 1
- 235000004443 Ricinus communis Nutrition 0.000 claims 1
- 229920000591 gum Polymers 0.000 claims 1
- 239000007762 w/o emulsion Substances 0.000 claims 1
- 244000007835 Cyamopsis tetragonoloba Species 0.000 abstract 1
- 229920001971 elastomer Polymers 0.000 abstract 1
- 239000000499 gel Substances 0.000 description 10
- 244000303965 Cyamopsis psoralioides Species 0.000 description 5
- 239000008247 solid mixture Substances 0.000 description 4
- LEACJMVNYZDSKR-UHFFFAOYSA-N 2-octyldodecan-1-ol Chemical compound CCCCCCCCCCC(CO)CCCCCCCC LEACJMVNYZDSKR-UHFFFAOYSA-N 0.000 description 3
- GHVNFZFCNZKVNT-UHFFFAOYSA-N Decanoic acid Natural products CCCCCCCCCC(O)=O GHVNFZFCNZKVNT-UHFFFAOYSA-N 0.000 description 3
- 239000004166 Lanolin Substances 0.000 description 3
- BTFJIXJJCSYFAL-UHFFFAOYSA-N arachidyl alcohol Natural products CCCCCCCCCCCCCCCCCCCCO BTFJIXJJCSYFAL-UHFFFAOYSA-N 0.000 description 3
- 235000019197 fats Nutrition 0.000 description 3
- 239000000945 filler Substances 0.000 description 3
- 229940039717 lanolin Drugs 0.000 description 3
- 235000019388 lanolin Nutrition 0.000 description 3
- 150000003626 triacylglycerols Chemical class 0.000 description 3
- XMVBHZBLHNOQON-UHFFFAOYSA-N 2-butyl-1-octanol Chemical compound CCCCCCC(CO)CCCC XMVBHZBLHNOQON-UHFFFAOYSA-N 0.000 description 2
- 239000005632 Capric acid (CAS 334-48-5) Substances 0.000 description 2
- IAJILQKETJEXLJ-UHFFFAOYSA-N Galacturonsaeure Natural products O=CC(O)C(O)C(O)C(O)C(O)=O IAJILQKETJEXLJ-UHFFFAOYSA-N 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- IAJILQKETJEXLJ-RSJOWCBRSA-N aldehydo-D-galacturonic acid Chemical compound O=C[C@H](O)[C@@H](O)[C@@H](O)[C@H](O)C(O)=O IAJILQKETJEXLJ-RSJOWCBRSA-N 0.000 description 2
- 239000004359 castor oil Substances 0.000 description 2
- 235000019438 castor oil Nutrition 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 150000004676 glycans Chemical class 0.000 description 2
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 2
- 230000003993 interaction Effects 0.000 description 2
- 210000004400 mucous membrane Anatomy 0.000 description 2
- WWZKQHOCKIZLMA-UHFFFAOYSA-N octanoic acid Chemical class CCCCCCCC(O)=O WWZKQHOCKIZLMA-UHFFFAOYSA-N 0.000 description 2
- 229920000573 polyethylene Polymers 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 230000002335 preservative effect Effects 0.000 description 2
- ABEXEQSGABRUHS-UHFFFAOYSA-N 16-methylheptadecyl 16-methylheptadecanoate Chemical compound CC(C)CCCCCCCCCCCCCCCOC(=O)CCCCCCCCCCCCCCC(C)C ABEXEQSGABRUHS-UHFFFAOYSA-N 0.000 description 1
- RWKSBJVOQGKDFZ-UHFFFAOYSA-N 16-methylheptadecyl 2-hydroxypropanoate Chemical compound CC(C)CCCCCCCCCCCCCCCOC(=O)C(C)O RWKSBJVOQGKDFZ-UHFFFAOYSA-N 0.000 description 1
- GLCFQKXOQDQJFZ-UHFFFAOYSA-N 2-ethylhexyl 12-hydroxyoctadecanoate Chemical compound CCCCCCC(O)CCCCCCCCCCC(=O)OCC(CC)CCCC GLCFQKXOQDQJFZ-UHFFFAOYSA-N 0.000 description 1
- XULHFMYCBKQGEE-UHFFFAOYSA-N 2-hexyl-1-Decanol Chemical compound CCCCCCCCC(CO)CCCCCC XULHFMYCBKQGEE-UHFFFAOYSA-N 0.000 description 1
- WRUPARRPRIVURX-MRCUWXFGSA-N 2-octyldodecyl (z)-docos-13-enoate Chemical compound CCCCCCCCCCC(CCCCCCCC)COC(=O)CCCCCCCCCCC\C=C/CCCCCCCC WRUPARRPRIVURX-MRCUWXFGSA-N 0.000 description 1
- LNRUVXAPKCPQGX-UHFFFAOYSA-N 2-octyldodecyl benzoate Chemical compound CCCCCCCCCCC(CCCCCCCC)COC(=O)C1=CC=CC=C1 LNRUVXAPKCPQGX-UHFFFAOYSA-N 0.000 description 1
- HXVCOQUDJKMJQY-UHFFFAOYSA-N 2-octyldodecyl octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(CCCCCCCC)CCCCCCCCCC HXVCOQUDJKMJQY-UHFFFAOYSA-N 0.000 description 1
- CYSSSYKSBHKJQE-UHFFFAOYSA-N 2-undecylpentadecan-1-ol Chemical compound CCCCCCCCCCCCCC(CO)CCCCCCCCCCC CYSSSYKSBHKJQE-UHFFFAOYSA-N 0.000 description 1
- 240000002791 Brassica napus Species 0.000 description 1
- 235000004977 Brassica sinapistrum Nutrition 0.000 description 1
- VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical group CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 description 1
- 244000062730 Melissa officinalis Species 0.000 description 1
- 235000010654 Melissa officinalis Nutrition 0.000 description 1
- 239000005662 Paraffin oil Substances 0.000 description 1
- 239000004264 Petrolatum Substances 0.000 description 1
- 244000000231 Sesamum indicum Species 0.000 description 1
- 235000003434 Sesamum indicum Nutrition 0.000 description 1
- 244000044822 Simmondsia californica Species 0.000 description 1
- 235000004433 Simmondsia californica Nutrition 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000004480 active ingredient Substances 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 235000014121 butter Nutrition 0.000 description 1
- 239000003610 charcoal Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 239000006071 cream Substances 0.000 description 1
- 239000002781 deodorant agent Substances 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- 239000004519 grease Substances 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- MNWFXJYAOYHMED-UHFFFAOYSA-N heptanoic acid Chemical class CCCCCCC(O)=O MNWFXJYAOYHMED-UHFFFAOYSA-N 0.000 description 1
- IPCSVZSSVZVIGE-UHFFFAOYSA-M hexadecanoate Chemical compound CCCCCCCCCCCCCCCC([O-])=O IPCSVZSSVZVIGE-UHFFFAOYSA-M 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 125000003010 ionic group Chemical group 0.000 description 1
- 229940060384 isostearyl isostearate Drugs 0.000 description 1
- 239000000865 liniment Substances 0.000 description 1
- 150000002632 lipids Chemical class 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 230000005012 migration Effects 0.000 description 1
- 238000013508 migration Methods 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 230000003020 moisturizing effect Effects 0.000 description 1
- 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000005473 octanoic acid group Chemical class 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 229940066842 petrolatum Drugs 0.000 description 1
- 235000019271 petrolatum Nutrition 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 230000008719 thickening Effects 0.000 description 1
- 230000000699 topical effect Effects 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 239000011782 vitamin Substances 0.000 description 1
- 229940088594 vitamin Drugs 0.000 description 1
- 229930003231 vitamin Natural products 0.000 description 1
- 235000013343 vitamin Nutrition 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
Abstract
The invention relates to a thickened composition containing as a thickener a polysaccharide alkyl ether formed by units including at least two different osidic rings, each unit including at least one hydroxyl group substituted by a saturated hydrocarbon alkyl chain. The alkyl ether has in particular a molecular weight of more than 200,000 and is in particular a guar rubber alkyl ether with a degree of substitution of 2 to 3. The invention also relates to the use of this composition in the cosmetic, dermatological, veterinary and / or veterinary fields. or feed
Description
COMPOSITION THREATENED BY A POLYSACCHARIDE ALKILETER
Field of the invention
The present invention relates to a thickened composition containing a new fat phase thickener, intended in particular for the cosmetic and / or dermatological fields. The invention also relates to a use of this composition for the treatment, makeup and / or treatment of human skin and / or mucous membranes.
BACKGROUND OF THE INVENTION
In cosmetic or dermatological products, it is common to find a thickened fatty phase; this happens particularly in ointments, treatment gels or anhydrous gomants, solid compositions such as deodorants, balms and lipsticks. The thickening of the oils makes it possible in particular to limit the exudation of the oils from the solid compositions and, in addition, in the reds of REF: 24126
lips the migration of the red film on the lips. To remedy these problems, waxes or fillers have usually been used. Unfortunately, these waxes and fillers have a tendency to compound the composition, which is not always desirable. In particular, women are increasingly looking for bright red lips. On the other hand, it is known to thicken oils with polymeric thickeners. Unfortunately, known oil thickeners must be used in large quantities to obtain a high viscosity gel, namely greater than 1.3 Pa. s. However, too large a quantity of thickener gives the composition, when the latter is intended for the cosmetic field, insufficient properties, particularly an adhesive touch and a lack of slippage, these disadvantages can be very annoying, even redhibitory.
Description of the invention
Surprisingly and unexpectedly, the applicant firm has discovered that it was possible
thickly thicken some fatty phases and obtain stable cosmetic compositions in transparent gel form having satisfactory cosmetic properties, thanks to a particular thickener. The subject of the present invention is therefore a composition comprising a fatty phase and a thickener of said fat phase, said thickener comprising at least one polysaccharide alkyl ether composed of units comprising at least two different osidic rings, each ring including at least one ring hydroxyl group substituted by a saturated hydrocarbon alkyl chain, and the fat phase having the solubility parameters dD and da according to the Hansen solubility space satisfactory under the following conditions: 15.00 (J / cm3) 1 2 < dD < 18.00 (J / cm3) 1 2 6.50 (J / cm3) 1 2 < da < 10, 00 (J / cm3) 1/2 Thanks to this particular thickener and this grease phase selection, the composition according to the invention is transparent and has a viscosity of more than 1.3 Pa.s (1300 cps) for a percentage of 4% weight. Thanks to this thickener and this selection of fatty substances, it is possible
bar-like solid composition exhibiting improved cosmetic properties in relation to the thickened compositions of the prior art. In particular, it is possible to obtain a soft red lipstick in the application that does not burn on the skin contiguous to the lips and with a shiny appearance. Although the invention is very particularly adapted to the cosmetic field, it applies to any field that needs to obtain thick compositions including solid compositions and particularly in the fields of agri-food, veterinary, dermatological, pharmaceutical, wood, (bar of pigments and wax) for the restoration of furniture). Preferably, 16.00 (J / cm3) 1 2 < dD < 18.00 (J / cm3) 1/2. The subject of the invention is also the use of a polysaccharide alkyl ether formed by units including at least two different osidic rings, each unit including at least one hydroxyl group substituted by a saturated hydrocarbon alkyl chain, to thicken a fatty phase having the parameters of solubility dD and da
according to the Hansen solubility space, which meets the following conditions: 15.00 (J / cm3) 1/2 < dD < 18.00 (J / cm3) 1 2 6.50 (J / cm3) 1/2 < da < 10.00 (J / cm3) 1/2. The definition of the fatty bodies in the space of three-dimensional solubility according to Hansen is described in the article by C.M. HANSEN: "The three dimensional solubility parameters" J. Paint Technol. 39, 105 (1967). According to Hansen's space: - dD characterizes the dispersion forces of LONDON from the formation of dipoles induced in molecular collisions; - dp characterizes the forces of DEBYE interactions between permanent dipoles; - dh characterizes the forces of specific interactions (type hydrogen bonds, acid / base, donor / acceptor, etc ...); - da is determined by the equation: da = (dp2 + dh2) 1 2 The parameters dp, dh- dD and da are expressed in (J / cm3) 1 2. In the composition according to the invention, any fatty substance can be used or mixture of bodies that comply with the indicated relationships
previously. In this case, the solubility parameters of the mixture are determined from those of the fatty substances taken separately, according to the following relationships: dDmel =? X Í dDi; dpme l = S X I dp i and dhme l = Í dhi gives the = (pmel + O hmel) where xi represents the volume fraction of the fatty body i in the mixture. Accordingly, it is possible to obtain thickened compositions particularly in gel form with a viscosity greater than 1.3 Pa.s with fatty substances whose solubility parameters are not included in the preceding relationships. It is within the scope of the person skilled in the art to determine the amounts of each fatty substance to obtain a mixture of fatty substances that complies with the aforementioned ratios. Fatty bodies that comply with the ratios indicated above include fatty acid triglycerides of 4 to 10 carbon atoms, such as triglycerides of heptanic acids (dD = 16.62 and da = 7.29), octanoic acids (dD). = 16.35 and da = 6.87), and capric / caprylic acids (dD = 16.64 and da = 6.69); synthetic oils having 12 to 26 carbon atoms such as octyldodecanol (dD = 16.36 and da = 7.69), 2-butyloctanol (dD =
16.12 and da = 9.78), 2-hexyldecanol (dD 16, 26 and da = 8.55), 2-undecylpentadecanol (dD = 16.45 and da = 6.79); esters of fatty acids particularly of 16 to 22 carbon atoms such as propylene glycol dioctanoate (dD = 16.07 and gives 6.68), neopentyl glycol diheptanoate (dD = 16.37 and da = 6.69), diethylene glycol diisononanoate (dD = 16.20 y = 6.86); the oleic alcohol (dD = 16.28 and da = 8.17); hydroxylated synthesis esters such as isostearyl lactate (dD = 16.36 and da = 8.74), octyl hydroxystearate (dD = 16.43 and da = 7.89), octyldodecyl hydroxystearate (dD = 16.54 and da = 6.56), diisostearyl malate (dD = 16.61 and da = 7.19), triisocetyl citrate (dD = 16.77 and da = 6.83); hydroxylated triglycerides such as castor oil (dD = 16.79 and da = 9.09), or also a mixture of one or more of these fatty substances. As fatty substances that do not comply with the Hansen ratios indicated above, taken separately, mention may be made of volatile silicones or not, oils of mineral origin such as petrolatum and paraffin oil, oils of vegetable origin such as oil jojoba, sesame, rapeseed, charcoal butter, synthetic oils such as Purcellin oil, palmitate
of 2-ethyl hexyl, 2-octyl dodecyl stearate, 2-octyl dodecyl erucate, isostearyl isostearate, 2-octyl dodecyl benzoate and hydrogenated isoparaffin (6, 8-moles of isobutylene). These oils do not comply with the ratios indicated above and are used at concentrations preferably not exceeding 50%. On the other hand, oils that comply with the Hansen ratios indicated above can represent up to 99% of the fatty phase. In the thickener of the invention, "saturated hydrocarbon alkyl chain" means a chain that includes from 1 to 24, preferably from 1 to 10 and better from 1 to 3 carbon atoms. In particular, the alkyl chain is selected from the methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, tert-butyl, n-pentyl chains. According to a preferred embodiment of the invention, the polysaccharide alkyl ether has a molecular weight greater than 100000, and preferably greater than 200000. This molecular weight can reach up to 1 million. This alkyl ether may include from one to six and better from two to four hydroxyl groups per
unit, substituted by a saturated hydrocarbon alkyl chain. The osidic cycles are chosen in particular between the oil, galactose, glucose, furanose, rhamnose, arabinose. According to a preferred embodiment of the invention, the polysaccharide alkyl ether according to the invention is an alkyl ether of a gum and more particularly of a globally non-ionic gum, that is to say it includes little or no ionic group. Suitable gums include, for example, guar gum, the unit of which comprises a galactose and a mannose, locust bean gum whose unit comprises a galactose and a mannose, araya gum which is a complex mixture of rhamnose, galactose, and galacturonic acid, the gum that is a complex mixture of arabinose, galactose and galacturonic acid. According to a preferred embodiment of the invention, the polysaccharide alkyl ether is a derivative of guar gum, and more particularly guartylated guar having a degree of substitution of 2 to 3 and particularly of about 2.5 as described in the document RD 95378007 (October 1995).
The composition according to the invention can contain, for example, an amount of alkyl ether of polysaccharide ranging from 0.5 to 10%, and preferably from 2 to 8% of the total weight of the composition. The composition according to the invention can also comprise all the ingredients conventionally used in the areas in question and more especially in the cosmetic and dermatological fields. These ingredients are in particular chosen from preservatives, vitamins and other lipophilic active ingredients (lanolin, UVA filter) or hydrophilic (moisturizing agents such as glycerin), different aqueous or fatty phase thickeners of the invention, perfumes, surfactants. , water, antioxidants, fillers, waxes, and their mixtures. The composition according to the invention can also contain lipid vesicles of the ionic and / or nonionic type. The amounts of these different ingredients are those conventionally used in the areas in question and for example from 0.01% to 20% of the total weight of the composition. The nature of these ingredients and their proportion must be compatible
with obtaining stable compositions thickened according to the invention. The composition of the invention can be presented in any of the galenic forms normally used for topical or oral application, and particularly in the form of an oily gel, an oil-in-water emulsion, or water-in-oil, a dispersion of oil in water thanks to vesicles, placing the vesicles between the oil / water contact surface. This composition can have the appearance of a cream, an ointment, a paste, an ointment, a bar. The composition according to the invention can advantageously be used for the treatment, makeup or treatment of the skin and / or mucous membranes depending on the nature of the active agents used. In particular, the composition of the invention can be a lipstick bar, a lip balm that can treat the cracks or also a composition to apply on the lipstick film particularly to increase its gloss. Also, the invention still has as its object a cosmetic use of the composition for caring for and / or applying the lips as well as a
use of this composition for the preparation of an ointment intended to treat the lips. The subject of the invention is also a cosmetic and / or dermatological treatment process for the lips, consisting of applying the composition defined above to the lips. The examples of compositions given below are hypothetical examples but fully realizable by the person skilled in the art; they are provided by way of illustration and without limitation. The quantities are given in% by weight.
Example 1
Guar ethylated with a degree of substitution of approximately 2.5 4% octyldodecanol cps 100%
The viscosity is 2.96 Pa.s (2960 cps).
This clear gel can be the basis for any cosmetic or dermatological composition.
Example 2
Ethyl guar having a degree of substitution of approximately 2.5 4% Triglycerides of acids csp 100% capric / caprylic
The viscosity is 2.91 Pa.s (2910 cps). This clear gel can be the basis for any cosmetic or dermatological composition.
Example 3
Guar ethylated with a degree of substitution of approximately 2.5 4%
Castor oil csp 100%
The viscosity is 67 Pa.s (67000 cps). This clear gel can be the basis for any cosmetic or dermatological composition.
Against example 1
With the C? -C? 5-alkylbenzoate whose solubility parameters dD and da are respectively
of 17.33 and 4.92, a liquid composition having a viscosity of 0.35 Pa.s (350 cps) by a 4% thickener is obtained. All the compositions indicated above were obtained by mixing the oil and the polymer by heating the mixture at 90 ° C until complete dissolution of the polymer. The gel was obtained by cooling to room temperature.
Example 4: Red lips
Ethyl guar with a degree of substitution of approximately 2.5 2.60%
Octyldodecanol 31.20% Capric / capric acid triglycerides 31.20%
Polyethylene (zero) 15.00%
Lanolin 10.00% pigments 10.00%
Perfume csp Preservative csp
From the clear gel prepared as above, polyethylene wax, lanolin and pigments were added at 90 ° C. After grinding the pigments and adding the perfume and
of the preservative, the red of lips is poured in a mold of suitable form to obtain a bar. It is noted that in relation to this date, the best method known by the applicant to carry out the present invention is that which is clear from the present description of the invention. Having described the invention as above, the content of the following is claimed as property:
Claims (22)
1. Composition containing a fatty phase and a thickener of said fat phase, characterized in that the thickener comprises at least one polysaccharide alkyl ether formed by units comprising at least two different osidic rings, each motif including at least one hydroxyl group substituted by a chain saturated hydrocarbon alkyl, and the fatty phase presents the solubility parameters dD and da according to the Hansen solubility space, fulfilling the following conditions: 15.00 (J / cm3) 1 2 < dD < 18.00 (J / cm3) 1 2 6.50 (J / cm3) 1 2 < da < 10.00 (J / cm3) 1 2.
2. Composition according to claim 1, characterized in that the solubility parameter dD is such as 16.00 (J / cm3) 1/2 < dD < 18.00 (J / cm3) 1 23.
Composition according to claim 1 or 2. characterized in that two of four hydroxyl groups per unit are replaced by a saturated hydrocarbon alkyl chain.
4. Composition according to one of the preceding claims, characterized in that the saturated hydrocarbon alkyl chain comprises from 1 to 24 carbon atoms.
5. Composition according to one of the preceding claims, characterized in that the saturated hydrocarbon alkyl chain includes from 2 to 10 carbon atoms.
6. Composition according to one of the preceding claims, characterized in that the alkyl chain is chosen from the methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, tert-butyl chains.
7. Composition according to one of the preceding claims, characterized in that the osidic cycles are chosen from mannose, galactose, glucose, furanose, rhamnose, arabinose.
8. Composition according to one of the preceding claims, characterized because the polysaccharide alkyl ether is an alkyl ether of a gum selected from guar gum, locust bean gum, karaya gum, gum trapping and their mixtures.
9. Composition according to one of the preceding claims, characterized in that the polysaccharide alkyl ether is ethyl chain guar gum with a degree of substitution of 2 to 3.
10. Composition according to one of the preceding claims, characterized in that the polysaccharide alkyl ether has a molecular weight higher than 200000.
11. Composition according to one of the preceding claims, characterized in that the polysaccharide alkyl ether is present in an amount ranging between 0.5 and 10% of the total weight of the composition.
12. Composition according to one of the preceding claims, characterized in that the polysaccharide alkyl ether is present in an amount ranging from 2 to 8% of the total weight of the composition.
13. Composition according to one of the preceding claims, characterized in that the fatty phase contains at least one fatty substance which complies with the Hansen ratios selected from the fatty acid triglycerides of 4 to 10 carbon atoms, having the synthesis oils of 12 at 26 carbon atoms, propylene glycol dioctanoate), neopentyl glycol diheptanoate, diethylene glycol diisononanoate, oleic alcohol, isostearyl lactate octyl hydroxystearate, octyldodecyl hydroxystearate, diisostearyl malate), triisocetyl citrate, Castor and its mixtures.
14. Composition according to the preceding claim, characterized in that the fatty body that complies with the Hansen ratios represents up to 99% of the fatty phase.
15. Composition according to one of the preceding claims, characterized because it comes in the form of an oily gel, a water-in-oil emulsion or an oil-in-water emulsion or an oil-in-water dispersion thanks to vesicles.
16. Composition according to one of the preceding claims, characterized in that it also contains at least one ingredient selected from perfumes, preservatives, waxes, pigments, lipophilic active agents.
17. Composition according to one of the preceding claims, characterized in that it is in the form of a bar of lipstick, lip balm or composition to be applied on a film of lipstick particularly to increase the gloss.
18. Use of a polysaccharide alkyl ether formed of units including at least two different osidic rings, each unit including at least one hydroxyl group substituted by a saturated hydrocarbon alkyl chain, to thicken a fatty phase having the parameters of solubility dD Y gives according to the Hansen solubility space that meets the following conditions: 15.00 (J / cm3) 1 2 < dD < 18.00 (J / cm3) 1/2 6.50 (J / cm3) 1 2 < da < 10.00 (J / cm3) 1 2.
19. Use according to claim 18, characterized in that the polysaccharide alkyl ether is an alkyl ether of a gum selected from guar gum, locust bean gum, karaya gum, gum gum and mixtures thereof.
20. Cosmetic use of the composition according to one of claims 1 to 17 to treat and / or make up the lips.
21. Use of the composition according to one of claims 1 to 17 for the preparation of an ointment intended to treat the lips.
22. Process for cosmetic treatment of the lips, characterized in that it consists of applying a composition on the lips as defined in claims 1 to 17.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR9603097A FR2746107B1 (en) | 1996-03-12 | 1996-03-12 | COMPOSITION THICKENED BY A POLYSACCHARIDE ALKYLETHER |
FR96-03097 | 1996-03-12 | ||
FR9603097 | 1996-03-12 |
Publications (2)
Publication Number | Publication Date |
---|---|
MXPA97001609A true MXPA97001609A (en) | 1998-04-01 |
MX9701609A MX9701609A (en) | 1998-04-30 |
Family
ID=9490103
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
MX9701609A MX9701609A (en) | 1996-03-12 | 1997-03-03 | Composition thickened by a polysaccharide alkylether. |
Country Status (7)
Country | Link |
---|---|
EP (1) | EP0795322B1 (en) |
JP (1) | JP2983487B2 (en) |
CA (1) | CA2198922A1 (en) |
DE (1) | DE69700041T2 (en) |
ES (1) | ES2126408T3 (en) |
FR (1) | FR2746107B1 (en) |
MX (1) | MX9701609A (en) |
Families Citing this family (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2767718B1 (en) | 1997-08-28 | 1999-10-22 | Oreal | WATER-IN-OIL EMULSION INCLUDING PYROGENATED SILICA AND POLYSACCHARIDE ALKYLETHER |
FR2768357B1 (en) | 1997-09-18 | 1999-11-05 | Snecma | METHOD OF ASSEMBLING OR RECHARGING BY BRAZING-DIFFUSING PARTS IN TITANIUM ALUMINIURE |
FR2783171B1 (en) | 1998-09-16 | 2000-11-17 | Oreal | EMULSION CONSISTING OF A HYDROPHILIC THICKENING COMPOUND AND A POLYSACCHARIDE ALKYLETHER, COMPOSITIONS CONSISTING OF THE SAID EMULSION, AND USES |
CN1316896A (en) * | 1998-09-11 | 2001-10-10 | 赫尔克里士公司 | Rheology modified compositions and processes thereof |
FR2783159B1 (en) | 1998-09-16 | 2000-11-17 | Oreal | EMULSION CONSISTING OF A HYDROPHILIC THICKENING COMPOUND AND A THICKNING COPOLYMER, COMPOSITIONS CONSISTING OF THE SAID EMULSION, AND USES |
FR2785529A1 (en) * | 1998-11-09 | 2000-05-12 | Oreal | COSMETIC NON-TRANSFER COMPOSITION COMPRISING A DISPERSION OF POLYMER PARTICLES IN A LIQUID FATTY PHASE |
US6517823B1 (en) | 2000-01-27 | 2003-02-11 | L'oreal S.A. | High gloss mascara |
WO2002047624A1 (en) | 2000-12-12 | 2002-06-20 | L'oreal Sa | Cosmetic compositions containing at least one heteropolymer and at least one gelling agent and methods of using the same |
US6835399B2 (en) | 2000-12-12 | 2004-12-28 | L'ORéAL S.A. | Cosmetic composition comprising a polymer blend |
CN100415202C (en) | 2000-12-12 | 2008-09-03 | 莱雅公司 | Cosmetic composition comprising a mixture of polymers |
FR2825618B1 (en) * | 2001-06-07 | 2008-01-18 | Oreal | USE OF A POLAR ADDITIVE IN A COSMETIC COMPOSITION COMPRISING A LIQUID FATTY PHASE STRUCTURED BY AT LEAST ONE ORGANOGELER TO GIVE THE COMPOSITION A THIXOTROPIC CHARACTER |
ITMI20011532A1 (en) | 2001-07-19 | 2003-01-19 | Intercos Italiana | SOLID COSMETIC |
FR2841467B1 (en) * | 2002-06-28 | 2006-01-20 | Oreal | COSMETIC COMPOSITION COMPRISING QUATERNARY SILICONE, A CATION, TWO CATIONIC POLYMERS AND COSMETIC PROCESSING PROCESS |
FR3048179B1 (en) | 2016-02-29 | 2019-08-23 | L'oreal | COMPOSITION COMPRISING ALKYL ETHER OF ALKYL POLYSACCHARIDE AND INCOMPATIBLE SILICONE OR FLUORINE OILS AND METHOD FOR CARRYING OUT SAID METHOD |
FR3048178A1 (en) * | 2016-02-29 | 2017-09-01 | Oreal | COMPOSITION COMPRISING POLYSACCHARIDE ALKYL ETHER AND INCOMPATIBLE OILS AND PROCESS FOR CARRYING OUT THE SAME |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4870167A (en) * | 1987-03-02 | 1989-09-26 | Hi-Tek Polymers, Inc. | Hydrophobically modified non-ionic polygalactomannan ethers |
ES2114280T3 (en) * | 1994-04-25 | 1998-05-16 | Oreal | USE OF A NON-IONIC OR ANIONIC GUAR GUM IN A NON-PERMANENT CONFORMATION PROCEDURE OF KERATINIC FIBERS. |
US5872246A (en) * | 1994-10-17 | 1999-02-16 | Aqualon Company | Ethyl guar |
-
1996
- 1996-03-12 FR FR9603097A patent/FR2746107B1/en not_active Expired - Fee Related
-
1997
- 1997-02-03 ES ES97400241T patent/ES2126408T3/en not_active Expired - Lifetime
- 1997-02-03 DE DE1997600041 patent/DE69700041T2/en not_active Expired - Fee Related
- 1997-02-03 EP EP19970400241 patent/EP0795322B1/en not_active Expired - Lifetime
- 1997-02-28 CA CA 2198922 patent/CA2198922A1/en not_active Abandoned
- 1997-03-03 MX MX9701609A patent/MX9701609A/en unknown
- 1997-03-11 JP JP9056664A patent/JP2983487B2/en not_active Expired - Lifetime
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