Self-invertible inverse latex comprising polyglycyerol esters, use thereof as a thickening agent, and cosmetic compositions comprising same
12251453 · 2025-03-18
Assignee
Inventors
- Miruna Bodoc (Lavaur, FR)
- Georges Da Costa (Saix, FR)
- Jérôme GUILBOT (Castres, FR)
- Aurélie PIERRE (MARLY LE ROI, FR)
Cpc classification
C08F222/385
CHEMISTRY; METALLURGY
A61K8/8158
HUMAN NECESSITIES
C08F220/585
CHEMISTRY; METALLURGY
C08F222/385
CHEMISTRY; METALLURGY
C08F220/585
CHEMISTRY; METALLURGY
C08F220/06
CHEMISTRY; METALLURGY
C08F220/06
CHEMISTRY; METALLURGY
A61K8/8188
HUMAN NECESSITIES
International classification
A61K8/81
HUMAN NECESSITIES
C08F220/06
CHEMISTRY; METALLURGY
C08F220/58
CHEMISTRY; METALLURGY
Abstract
The invention relates to a self-invertible inverse latex comprising, as an inverting agent, surfactant species of the polyglycerol ester family, the alkyl chain of which has from 8 to 18 carbon atoms, with polyglycerols having 1 to 10 glycerol units, and the use thereof as a thickening and/or emulsifying and/or stabilizing agent for a cosmetic, dermopharmaceutical or pharmaceutical topical composition, and cosmetic, dermopharmaceutical or pharmaceutical topical compositions comprising same. Also disclosed are surfactant compositions comprising polyglycerol esters, the alkyl chain of which has from 8 to 18 carbon atoms, and polyglycerols having 1 to 10 glycerol units.
Claims
1. A self-invertible inverse latex of a crosslinked anionic polyelectrolyte (P) comprising, per 100 mol %: (a.sub.1)a proportion of greater than or equal to 25 mol % and less than or equal to 80 mol % of monomer units derived from 2-methyl-2-[(1-oxo-2-propenyl)amino]-1-propanesulfonic acid in free acid or partially or totally salified form; (a.sub.2)a proportion greater than or equal to 20 mol % and less than or equal to 75 mol % of monomer units derived from at least one monomer chosen from the elements of the group consisting of acrylamide, N,N-dimethyl acrylamide; methacrylamide or N-isopropylacrylamide; (a.sub.3)optionally a proportion of greater than 0 mol % and less than or equal to 10%, of monomer units derived from at least one monomer chosen from the elements of the group consisting of acrylic acid, methacrylic acid, 2-carboxyethylacrylic acid, itaconic acid, maleic acid, 3-methyl-3-[(1-oxo-2-propenyl)amino]butanoic acid, the carboxylic function of said monomers being in free acid or partially or totally salified form; (a.sub.4)a proportion of greater than 0 mol % and less than or equal to 1 mol % of monomer units derived from at least one diethylenic or polyethylenic crosslinking monomer (AR); the sum of said molar proportions of a.sub.1), a.sub.2), a.sub.3) and a.sub.4) being equal to 100 mol %; said self-invertible inverse latex in the form of a water-in-oil emulsion () comprising, per 100% of its weight: a)from 10% by weight to 90% by weight of said crosslinked anionic polyelectrolyte (P); b)from 5% by weight to 50% by weight of a fatty phase constituted of at least one oil (0); c)from 1% by weight to 50% by weight of water; d)from 0.5% by weight to 10% by weight of a water-in-oil emulsifying system (S.sub.1); and e)from 2% by weight to 10% by weight of an oil-in-water emulsifying system (S.sub.2); the sum of the weight proportions of a), b), c), d) and e) being equal to 100% by weight; wherein said oil-in-water emulsifying system (S.sub.2) comprises, per 100% of its weight: f)a proportion of greater than or equal to 50% by weight and less than or equal to 100% of a composition (C.sub.e) which comprises, per 100% of its weight: e.sub.1)from 5% by weight to 15% by weight of at least one compound of formula (I):
HO[CH.sub.2CH(OH)CH.sub.2O].sub.nH(I) wherein n represents an integer greater than or equal to 1 and less than or equal to 15; e.sub.2)from 60% by weight to 80% by weight of at least one compound of formula (II):
R.sub.1(CO)[OCH.sub.2CH(OH)CH.sub.2].sub.pOH(II), wherein p, which is different than or identical to n, represents an integer greater than or equal to 1 and less than or equal to 15; and in which the group R.sub.1(CO) represents a saturated or unsaturated, linear or branched aliphatic radical including from 6 to 22 carbon atoms; and es)from 5% by weight to 15% by weight of at least one composition (C.sub.11) represented by the formula (III):
HO[CH.sub.2CHOHCH.sub.2O].sub.q-(G).sub.r-H(III), wherein q, which is different than or identical to n, represents an integer greater than or equal to 1 and less than or equal to 3, G represents a reducing sugar residue and r represents a decimal number greater than or equal to 1.05 and less than or equal to 5.00; said composition (C.sub.11) consisting of a mixture of the compounds of formulae (III.sub.1), (III.sub.2), (III.sub.3), (III.sub.4) and (III.sub.5):
HO[CH.sub.2CHOHCH.sub.2O].sub.qO-(G)-H(III.sub.1),
HO[CH.sub.2CHOHCH.sub.2O].sub.qO-(G).sub.2-H(III.sub.2),
HO[CH.sub.2CHOHCH.sub.2O].sub.qO-(G).sub.3-H(III.sub.3),
HO[CH.sub.2CHOHCH.sub.2O].sub.qO-(G).sub.4-H(III.sub.4),
HO[CH.sub.2CHOHCH.sub.2O].sub.qO-(G).sub.5-H(III.sub.5), in molar proportions of said compounds of formulae (III.sub.1), (III.sub.2), (III.sub.3), (III.sub.4) and (III.sub.5) respectively equal to a.sub.1, a.sub.2, as, a.sub.4 and a.sub.5, such that the sum (a.sub.1+a.sub.2+a.sub.3+a.sub.4+a.sub.5) is equal to 1, and such that the sum (a.sub.1+2a.sub.2+3a.sub.3+4a.sub.4+5a.sub.5) is equal to r; the sum of the weight proportions of e.sub.1), e.sub.2) and e.sub.3) being equal to 100% by weight.
2. The self-invertible inverse latex as defined in claim 1, wherein, in said oil-in-water emulsifying system (S.sub.2), said composition (C.sub.e) consists of, per 100% of its weight: e.sub.1)from 5% by weight to 15% by weight of at least one compound of formula (I), e.sub.2)from 60% by weight to 80% by weight of at least one compound of formula (II), and e.sub.3)from 5% by weight to 15% by weight of at least one composition (C.sub.11) represented by the formula (III); and wherein said crosslinked anionic polyelectrolyte (P) is a copolymer crosslinked with triallylamine and/or methylenebis(acrylamide), of 2-methyl-2-[(1-oxo-2-propenyl)amino]-1-propanesulfonic acid () partially or totally salified in the form of a sodium salt or ammonium salt, and of acrylamide (), in a ()/() molar ratio greater than or equal to 25/75 and less than or equal to 80/20; a copolymer crosslinked with triallylamine and/or methylenebis(acrylamide), of 2-methyl-2-[(1-oxo-2-propenyl)amino]-1-propanesulfonic acid () partially or totally salified in the form of a sodium salt, and of acrylamide (), in a ()/() molar ratio greater than or equal to 30/70 and less than or equal to 80/20; a copolymer crosslinked with triallylamine and/or methylenebis(acrylamide), of 2-methyl-2-[(1-oxo-2-propenyl)amino]-1-propanesulfonic acid () partially or totally salified in the form of a sodium salt, and of acrylamide (), in a ()/() molar ratio greater than or equal A to 40/60 and less than or equal to 80/20; a terpolymer crosslinked with triallylamine and/or methylenebis(acrylamide), of 2-methyl-2-[(1-oxo-2-propenyl)amino]-1-propanesulfonic acid partially or totally salified in the form of a sodium salt or ammonium salt in a molar proportion greater than or equal to 30% and less than or equal to 45%, of acrylamide in a molar proportion greater than or equal to 45% and less than or equal to 68% and of acrylic acid partially or totally salified in the form of a sodium salt or ammonium salt in a molar proportion greater than or equal to 2% and less than or equal to 10%, or a terpolymer crosslinked with triallylamine and/or methylenebis(acrylamide), of 2-methyl-2-[(1-oxo-2-propenyl)amino]-1-propanesulfonic acid partially or totally salified in the form of a sodium salt or ammonium salt in a molar proportion greater than or equal to 30% and less than or equal to 45%, of acrylamide in a molar proportion greater than or equal to 47% and less than or equal to 68% and of acrylic acid partially or totally salified in the form of a sodium salt or ammonium salt in a molar proportion greater than or equal to 2% and less than or equal to 8%.
3. The self-invertible inverse latex in the form of a water-in-oil emulsion as defined in claim 1, wherein, in said oil-in-water emulsifying system (S.sub.2), said composition (C.sub.e) consists of, per 100% of its weight: e.sub.1)from 5% by weight to 15% by weight of at least one compound of formula (I), e.sub.2)from 60% by weight to 80% by weight of at least one compound of formula (II), and e.sub.3)from 5% by weight to 15% by weight of at least one composition (C.sub.11) represented by the formula (III); and, wherein, in formula (I), n represents an integer greater than or equal to 1 and less than or equal to 10, and wherein, in formula (II), p, which may be identical to or different than n, represents an integer greater than or equal to 1 and less than or equal to 10, and the group R.sub.1(CO) is chosen from octanoyl, decanoyl, -undecylenoyl, dodecanoyl, tetradecanoyl, hexadecanoyl, octadecanoyl, 9-octadecenoyl and 9,12-octadecadienoyl radicals.
4. The self-invertible inverse latex in the form of a water-in-oil emulsion as defined in claim 1, wherein, in said oil-in-water emulsifying system (S.sub.2), said composition (C.sub.e) consists of, per 100% of its weight: e.sub.1)from 5% by weight to 15% by weight of at least one compound of formula (I), e.sub.2)from 60% by weight to 80% by weight of at least one compound of formula (II), and e.sub.3)from 5% by weight to 15% by weight of at least one composition (C11) represented by the formula (III); and wherein, in the formula (III), q is equal to 1, G represents the residue of glucose and r represents a decimal number greater than or equal to 1.05 and less than or equal to 2.5.
Description
DESCRIPTION OF THE PREFERRED EMBODIMENTS
IPreparation of Surface-Active Compositions According to the Invention and Comparative Compositions
(1) I.sub.APreparation of the Composition (EM.sub.2) Based on Decaglycerol Laurate (EM.sub.1) and on Hexaglycerol
(2) 71.5 grams of decaglycerol monolaurate sold under the brand name Decaglyn 1-L (hereinafter denoted by the term Composition (EM.sub.1)) and 28.5 grams of polyglycerol-6 (sold under the brand name Polyglycerol 6 by Spiga) are introduced into a jacketed glass reactor provided with efficient mechanical stirring, in which jacket a heat-exchange fluid circulates, at a temperature of 35 C. under mechanical stirring of anchor type at a speed of 80 revolutions/minute. After stirring under such conditions for 30 minutes, the mixture is emptied out to obtain composition (EM.sub.2).
(3) I.sub.B Preparation of Composition (EM.sub.3) Based on Decaglycerol Laurate (EM.sub.1) and Decaglycerol
(4) 71.5 grams of decaglycerol monolaurate sold under the brand name Decaglyn 1-L (hereinafter denoted by the term Composition (EM.sub.1)) and 28.5 grams of polyglycerol-10 (sold under the brand name Polyglycerin 10) are introduced into a jacketed glass reactor provided with efficient mechanical stirring, in which jacket a heat-exchange fluid circulates, at a temperature of 35 C. under mechanical stirring of anchor type at a speed of 80 revolutions/minute. After stirring under such conditions for 30 minutes, the mixture is emptied out to obtain composition (EM.sub.3).
(5) The analytical characteristics of compositions (EM.sub.1), (EM.sub.2) and (EM.sub.3) are given in table 1 below.
(6) TABLE-US-00001 TABLE 1 Emulsifying composition Proportions of constituents (weight %) (EM.sub.1) (EM.sub.2) (EM.sub.3) Decaglycerol monolaurate 100% 71.5% 71.5% Weight proportion of hexaglycerol 0% 28.5 0% Weight proportion of decaglycerol 0% 0% 28.5
IIPreparation and Evaluation of Self-Inverting Inverse Latexes of a Crosslinked Terpolymer of the Sodium Salt of 2-Methyl-[(1-Oxo-2-Propenyl)Amino]-1-Propanesulfonic Acid, of Acrylamide and of Partially Salified Acrylic Acid and of a Self-Inverting Inverse Latex of a Crosslinked Copolymer of the Sodium Salt of 2-Methyl-[(1-Oxo-2-Propenyl)Amino]-1-Propanesulfonic Acid and of Acrylamide
(7) II-a)An aqueous phase is prepared by successively pouring, into a beaker and with stirring, 277 grams of a commercial solution containing 50% by weight of acrylamide, 375 grams of an aqueous solution containing 55% of the sodium salt of 2-methyl-[(1-oxo-2-propenyl)amino]-1-propanesulfonic acid, 10.8 grams of glacial acrylic acid, 0.058 gram of methylenebis(acrylamide), 0.45 gram of a commercial aqueous solution containing 40% by weight of sodium diethylenetriamine pentaacetate, and 5.3 grams of an aqueous solution containing 48% by weight of sodium hydroxide to adjust the pH of this aqueous phase to 5.3.
(8) An organic phase is independently prepared by mixing 130 grams of polyisobutene, 90 grams of Isopar H, 30 grams of Marcol 52, 17.0 grams of Montane 70, 5 grams of Simaline IE 200 and 0.2 gram of azobis(isobutyronitrile) (AIBN).
(9) The aqueous phase prepared is subsequently gradually added to the oily phase and then dispersed using a rotor-stator of Ultra-Turrax type sold by the company IKA.
(10) The emulsion obtained is transferred into a reactor, subjected to sparging with nitrogen to remove the oxygen, and cooled to about 5-6 C. 5 cm.sup.3 of a solution containing 0.42% by weight of cumene hydroperoxide in Isopar H are added to the emulsion with continuous stirring, followed by gradual introduction of an aqueous solution containing 0.1% by weight of sodium metabisulfite at a flow rate of 0.5 cm.sup.3 per minute to initiate the polymerization reaction. The temperature of the medium increases up to a steady stage.
(11) After maintaining at 80 C. for one hour, the Isopar H is removed from the reaction medium by partial vacuum distillation, as is most of the water. The reaction medium is then cooled to approximately 35 C. to obtain the mixture denoted (M.sub.1).
(12) The mixture (M.sub.1) obtained above is divided up into different portions, to which the different surface-active compositions (EM.sub.1), (EM.sub.2) and (EM.sub.3), as described above, preheated to 60 C., are added in proportions by weight as shown in table 2 below.
(13) The self-invertible inverse latexes resulting from these mixtures are respectively denoted (IL.sub.1), (IL.sub.2) and (IL.sub.3) and are evaluated by the observation of their appearance at 25 C., by the rate of inversion during the preparation of an aqueous gel comprising 2% by weight of self-invertible inverse latex (the method of which is described below) and by the viscosity of this aqueous gel comprising 2% by weight of a self-invertible inverse latex.
(14) The method for evaluation of the duration of inversion of the self-invertible inverse latexes consists in introducing, into a 2 liter beaker, the amount of water necessary for the preparation of 800 grams of an aqueous gel. A mechanical helical stirrer of Turbotest type, version 2004, sold by the company VMI, connected to a motor, is placed toward the bottom of the beaker. Stirring is started at a speed of 900 revolutions/minute and the necessary amount of self-invertible inverse latex to be evaluated is introduced into the beaker with stirring. This stirring creates a vortex which disappears when the polymer inverts and the gel is formed. The duration of inversion, measured in seconds, of the self-invertible inverse latexes corresponds to the time elapsed between the start of the addition of the self-invertible inverse latex tested and the disappearance of the vortex, resulting in a smooth gel, devoid of lumps, being obtained. This evaluation is carried out on conclusion of the manufacture of the inverse latexes tested (t=0) and then after a period of storage at 25 C. of 2 months (t=2 months). The results obtained are given in table 2 below. The viscosity of an aqueous gel comprising 2% by weight of self-invertible inverse latex () is measured at t=0 and then at t=2 months, by means of a Brookfield RVT viscometer (Spindle 6 Speed 5). Likewise, the appearance of the self-invertible inverse latex is evaluated visually at t=0.
(15) TABLE-US-00002 TABLE 2 Self-invertible inverse latexes (IL.sub.1) (IL.sub.2) (IL.sub.3) Reference of the test surfactant composition (EM.sub.1) (EM.sub.2) (EM.sub.3) Amount tested (EMi)/(ILi) 5% 7% 7% (weight %) Measured at t = 0 (in mPa .Math. s) 91.000 90.000 75.000 Duration of inversion 82 s 22 s 14 s Appearance of the self- Mle* Mle* Mle* invertible latex at 25 C. Measured at t = 2 months (in mPa .Math. s) 62.000 65.000 77.000 Duration of inversion 142 s 22 s 12 s Mle*: Milky liquid emulsion
(16) The self-invertible inverse latexes (IL.sub.2) and (IL.sub.3) according to the invention and free of alkoxylated derivatives make it possible to obtain smooth gels, with a duration of inversion far lower than that observed for the self-invertible inverse latex (IL.sub.1), comprising only decaglycerol monolaurate alone as constituent of the inverting surface-active system, while retaining excellent thickening properties. Furthermore, they are characterized by better reproducibility of the rate of inversion and of the thickening properties after two months of storage than for the comparative self-invertible inverse latex (IL.sub.1).
IIIPreparation and Evaluation of Self-Invertible Inverse Latexes of a Crosslinked Copolymer of the Sodium Salt of 2-Methyl-2-[(1-Oxo-2-Propenyl)Amino]-1-Propanesulfonic Acid and of Acrylamide
(17) An aqueous phase is prepared by successively pouring, into a beaker and with stirring, 255 grams of a commercial solution containing 50% by weight of acrylamide, 272 grams of an aqueous solution containing 55% of the sodium salt of 2-methyl-[(1-oxo-2-propenyl)amino]-1-propanesulfonic acid, 0.107 grams of methylenebis(acrylamide), 0.45 gram of a commercial aqueous solution containing 40% by weight of sodium diethylenetriamine pentaacetate, and 45 grams of an aqueous solution containing 48% by weight of sodium hydroxide to adjust the pH of this aqueous phase to 6.0.
(18) An organic phase is independently prepared by mixing 220 grams of Emogreen L15 and 25 grams of Simaline IE.
(19) The aqueous phase prepared is subsequently gradually added to the oily phase and then dispersed using a rotor-stator of Ultra-Turrax type sold by the company IKA.
(20) The resulting emulsion is transferred to a reactor to be subjected to nitrogen bubbling in order to remove the oxygen and cooled to about 5-6 C. 0.69 gram of sodium persulfate dissolved beforehand in 2 grams of water is added to the emulsion, with the stirring being maintained, then an aqueous solution containing 2.25% by weight of sodium metabisulfite is gradually introduced in order to initiate the polymerization reaction. The temperature of the medium increases up to a steady stage.
(21) After maintaining at 80 C. for three hours, the reaction medium is then cooled to approximately 35 C. to obtain the mixture denoted (M.sub.2).
(22) The mixture (M.sub.2) obtained above is divided up into different portions, to which the different surface-active compositions (EM.sub.1), (EM.sub.2) and (EM.sub.3), as described above, preheated to 60 C., are added in proportions by weight as shown in table 3 below.
(23) The self-invertible inverse latexes resulting from these mixtures are respectively denoted (IL.sub.4), (IL.sub.5) and (IL.sub.6) and are evaluated by the observation of their appearance at 25 C., by the rate of inversion during the preparation of an aqueous gel comprising 2% by weight of self-invertible inverse latex (the method of which is described below) and by the viscosity of this aqueous gel comprising 2% by weight of a self-invertible inverse latex.
(24) The method for evaluation of the duration of inversion of the self-invertible inverse latexes consists in introducing, into a 2 liter beaker, the amount of water necessary for the preparation of 800 grams of an aqueous gel. A mechanical helical stirrer of Turbotest type, version 2004, sold by the company VMI, connected to a motor, is placed toward the bottom of the beaker. Stirring is started at a speed of 900 revolutions/minute and the necessary amount of self-invertible inverse latex to be evaluated is introduced into the beaker with stirring. This stirring creates a vortex which disappears when the polymer inverts and the gel is formed. The duration of inversion, measured in seconds, of the self-invertible inverse latexes corresponds to the time elapsed between the start of the addition of the self-invertible inverse latex tested and the disappearance of the vortex, resulting in a smooth gel, devoid of lumps, being obtained. This evaluation is carried out at the end of the production of the tested inverse latexes (t=0). The results obtained are given in table 3 below. The viscosity of an aqueous gel comprising 2% by weight of self-invertible inverse latex (M) is measured at t=0 by means of a Brookfield RVT viscometer (Spindle 6 Speed 5). Likewise, the appearance of the self-invertible inverse latex is evaluated visually at t=0.
(25) TABLE-US-00003 TABLE 2 Self-invertible inverse latexes (IL.sub.4) (IL.sub.5) (IL.sub.6) Reference of the test surfactant composition (EM.sub.1) (EM.sub.2) (EM.sub.3) Amount tested (EMi)/(ILi) 5% 7% 7% (weight %) Measured at t = 0 (in mPa .Math. s) 75.000 101.200 83.600 Duration of inversion 45 s 30 s 30 s Appearance of the self- Mle* Mle* Mle* invertible latex at 25 C. Mle*: Milky liquid emulsion
The self-invertible inverse latexes (IL.sub.5) and (IL.sub.6) according to the invention and free of alkoxylated derivatives make it possible to obtain, at t=0, smooth gels, with a duration of inversion lower than that observed for the self-invertible inverse latex (IL.sub.1), comprising only decaglycerol monolaurate alone as constituent of the inverting surface-active system, while retaining excellent thickening properties.
IV: Illustrative Cosmetic Formulations
(26) In the formulations below, the percentages are expressed as weight percentages per 100% of the weight of the formulation.
Example IV-1: Care Cream
(27) Cyclomethicone: 10% Self-invertible inverse latex (IL.sub.2): 0.8% Montanov 68: 2% Stearyl alcohol: 1% Stearic alcohol: 0.5% Preservative: 0.65% Lysine: 0.025% EDTA (disodium salt): 0.05% Xanthan gum: 0.2% Glycerol: 3% Water: q.s. 100%
Example IV-2: Antisun Milk
(28) Formula
(29) A Montanov 68: 3.0% Sesame oil: 5.0% Parsol MCX: 5.0% A-Carrageenan: 0.10% B Water: q.s. 100% C Self-invertible inverse latex (IL.sub.3): 0.80% D Fragrance: q.s. Preservative: q.s.
Procedure Emulsify B in A at 60 C., then add C at approximately 60 C., then D at approximately 30 C. and adjust the pH, if necessary.
Example IV-3: Body Milk
(30) Montanov 202: 3.5% Lanol 37T: 8.0% Solagum L: 0.05% Water: q.s. 100% Benzophenone-3: 2.0% Dimethicone 350 cPs: 0.05% Self-invertible inverse latex (IL.sub.2): 2.5% Preservative: 0.2% Fragrance: 0.4%
Example IV-4: Makeup-Removing Emulsion Comprising Sweet Almond Oil
(31) Montanov 202: 5% Sweet almond oil: 5% Water: q.s. 100% Self-invertible inverse latex (IL.sub.2): 0.3% Glycerol: 5% Preservative: 0.2% Fragrance: 0.3%
Example IV-5: Moisturizing Cream for Greasy Skin
(32) Montanov 68: 5% Cetylstearyl octanoate: 8% Octyl palmitate: 2% Water: q.s. 100% Self-invertible inverse latex (IL.sub.3): 2.6% Micropearl M100 3.0% Mucopolysaccharides: 5% Sepicide HB: 0.8% Fragrance: 0.3%
Example IV-6: Makeup-Removing Milk
(33) Montanov 68: 3% Primol 352: 8.0% Sweet almond oil: 2% Water: q.s. 100% Self-invertible inverse latex (IL.sub.2): 0.8% Preservative: 0.2%
Example IV-7: Antisun Milk
(34) Montanov L: 3.5% Lanol 37T: 10.0% Parsol MCX: 5.0% Eusolex 4360: 2.0% Water: q.s. 100% Self-invertible inverse latex (IL.sub.2): 1.8% Preservative: 0.2% Fragrance: 0.4%
Example IV-8: Sunless Tanning Emulsion
(35) Lanol 99: 15% Montanov 68: 3.0% Parsol MCX: 3.0% Water: q.s. 100% Dihydroxyacetone: 5.0% Monosodium phosphate: 0.2% Self-invertible inverse latex (IL.sub.3): 2.5% Fragrance: 0.3% Sepicide HB: 0.8% Sodium hydroxide: q.s. pH=5.
Example IV-9: Care Cream
(36) Cyclomethicone: 10% Self-invertible inverse latex (IL.sub.3): 2.8% Montanov 202: 4.5% Preservative: 0.65% Lysine: 0.025% EDTA (disodium salt): 0.05% Xanthan gum: 0.2% Glycerol: 3% Water: q.s. 100%
Example IV-10: Antisun Cream
(37) Simulsol 165: 3% Montanov 68: 2% C12-C15 benzoate: 8% Pecosil PS 100: 2% Dimethicone: 2% Cyclomethicone: 5% Octyl para-methoxycinnamate: 6% Benzophenone-3: 4% Titanium oxide: 8% Xanthan gum: 0.2% Butylene glycol: 5% Demineralized water: q.s. 100% Self-invertible inverse latex (IL.sub.2): 1.5% Preservative, fragrance: q.s.
Example IV-11: Suncare and Self-Tanning Gel
(38) Montanov 68: 3.0% Glyceryl triheptanoate: 10.0% Deepaline PVB: 1.05% Self-invertible inverse latex (IL.sub.3): 2.2% Water: q.s. 100% Dihydroxyacetone: 5% Fragrance: 0.1% Sepicide HB: 0.3% Sepicide Cl: 0.1% Parsol MCX: 4.0%
The definitions of the products used in the examples are as follows: Micropearl M 100 is an ultrafine powder which is very soft to the touch and which has a mattifying action, sold by the company Matsumo. Sepicide Cl, imidazolidinyl urea, is a preservative sold by the company SEPPIC. Simulsol 165 is self-emulsifying glycerol stearate, sold by the company SEPPIC. Sepicide HB, a mixture of phenoxyethanol, methylparaben, ethylparaben, propylparaben and butylparaben, is a preservative sold by the company SEPPIC. Parsol MCX is octyl para-methoxycinnamate, sold by the company Givaudan. Lanol 37T is glycerol triheptanoate, sold by the company SEPPIC. Solagum L is a carrageenan, sold by the company SEPPIC. Eusolex 4360 is a sunscreen, sold by the company Merck. Deepaline PVB is an acylated wheat protein hydrolyzate, sold by the company SEPPIC. Primol 352 is a mineral oil, sold by the company Exxon. Pecosil PS 100 is Dimethicone PEG-7, sold by the company Phoenix. Montanov 68 (INCI name: cetearyl alcohol (and) cetearyl glucoside) is an emulsifying agent, sold by the company SEPPIC. Montanov L (INCI name: C14-22 alcohols (and) C12-20 alkyl glucoside) is an emulsifying agent, sold by the company SEPPIC. Montanov 202 (INCI name: arachidyl alcohol (and) behenyl alcohol (and) arachidyl glucoside) is an emulsifying agent, sold by the company SEPPIC.