JPH03115207A - Oily composition and cosmetic containing same - Google Patents
Oily composition and cosmetic containing sameInfo
- Publication number
- JPH03115207A JPH03115207A JP25353989A JP25353989A JPH03115207A JP H03115207 A JPH03115207 A JP H03115207A JP 25353989 A JP25353989 A JP 25353989A JP 25353989 A JP25353989 A JP 25353989A JP H03115207 A JPH03115207 A JP H03115207A
- Authority
- JP
- Japan
- Prior art keywords
- oil
- oily
- water
- cosmetic
- polymer
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 49
- 239000002537 cosmetic Substances 0.000 title claims abstract description 36
- 229920001296 polysiloxane Polymers 0.000 claims abstract description 67
- 229920000642 polymer Polymers 0.000 claims abstract description 28
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 25
- 229920002545 silicone oil Polymers 0.000 claims abstract description 20
- 239000007787 solid Substances 0.000 claims abstract description 16
- 239000002734 clay mineral Substances 0.000 claims abstract description 9
- 150000005846 sugar alcohols Polymers 0.000 claims abstract description 8
- 229920003169 water-soluble polymer Polymers 0.000 claims abstract description 8
- 239000007788 liquid Substances 0.000 claims abstract description 7
- 239000000463 material Substances 0.000 claims description 11
- 239000003349 gelling agent Substances 0.000 claims description 9
- 238000002156 mixing Methods 0.000 abstract description 15
- 230000000694 effects Effects 0.000 abstract description 6
- 239000003795 chemical substances by application Substances 0.000 abstract description 3
- 238000004132 cross linking Methods 0.000 abstract description 3
- 239000002932 luster Substances 0.000 abstract 1
- 239000003921 oil Substances 0.000 description 53
- 235000019198 oils Nutrition 0.000 description 53
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 39
- 239000002585 base Substances 0.000 description 29
- -1 fatty acid esters Chemical class 0.000 description 29
- 235000014113 dietary fatty acids Nutrition 0.000 description 14
- 239000000194 fatty acid Substances 0.000 description 14
- 229930195729 fatty acid Natural products 0.000 description 14
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 12
- 125000001931 aliphatic group Chemical group 0.000 description 8
- 239000004615 ingredient Substances 0.000 description 7
- 238000004519 manufacturing process Methods 0.000 description 6
- 239000000047 product Substances 0.000 description 6
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 6
- 150000001875 compounds Chemical class 0.000 description 5
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 5
- 238000000034 method Methods 0.000 description 5
- 239000001993 wax Substances 0.000 description 5
- 230000003197 catalytic effect Effects 0.000 description 4
- 239000004205 dimethyl polysiloxane Substances 0.000 description 4
- 235000013870 dimethyl polysiloxane Nutrition 0.000 description 4
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 description 4
- XDOFQFKRPWOURC-UHFFFAOYSA-N 16-methylheptadecanoic acid Chemical compound CC(C)CCCCCCCCCCCCCCC(O)=O XDOFQFKRPWOURC-UHFFFAOYSA-N 0.000 description 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerol Natural products OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 3
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical group [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 3
- 229920002472 Starch Polymers 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 150000008044 alkali metal hydroxides Chemical class 0.000 description 3
- 125000003118 aryl group Chemical group 0.000 description 3
- 238000006482 condensation reaction Methods 0.000 description 3
- 239000006071 cream Substances 0.000 description 3
- 125000004122 cyclic group Chemical group 0.000 description 3
- 239000000839 emulsion Substances 0.000 description 3
- 150000002148 esters Chemical class 0.000 description 3
- 238000011156 evaluation Methods 0.000 description 3
- 150000004665 fatty acids Chemical class 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 3
- 238000006116 polymerization reaction Methods 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- 239000008213 purified water Substances 0.000 description 3
- 239000008107 starch Substances 0.000 description 3
- 235000019698 starch Nutrition 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 description 2
- LAIUFBWHERIJIH-UHFFFAOYSA-N 3-Methylheptane Chemical compound CCCCC(C)CC LAIUFBWHERIJIH-UHFFFAOYSA-N 0.000 description 2
- 239000004375 Dextrin Substances 0.000 description 2
- 229920001353 Dextrin Polymers 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- 239000004354 Hydroxyethyl cellulose Substances 0.000 description 2
- 239000004166 Lanolin Substances 0.000 description 2
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 2
- 229920002125 Sokalan® Polymers 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- 239000004359 castor oil Substances 0.000 description 2
- 235000019438 castor oil Nutrition 0.000 description 2
- 239000007795 chemical reaction product Substances 0.000 description 2
- 238000006356 dehydrogenation reaction Methods 0.000 description 2
- 235000019425 dextrin Nutrition 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- UKMSUNONTOPOIO-UHFFFAOYSA-N docosanoic acid Chemical compound CCCCCCCCCCCCCCCCCCCCCC(O)=O UKMSUNONTOPOIO-UHFFFAOYSA-N 0.000 description 2
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- 239000003205 fragrance Substances 0.000 description 2
- 235000011187 glycerol Nutrition 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
- BXWNKGSJHAJOGX-UHFFFAOYSA-N hexadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCO BXWNKGSJHAJOGX-UHFFFAOYSA-N 0.000 description 2
- 150000002430 hydrocarbons Chemical class 0.000 description 2
- 235000019447 hydroxyethyl cellulose Nutrition 0.000 description 2
- 235000019388 lanolin Nutrition 0.000 description 2
- 229940039717 lanolin Drugs 0.000 description 2
- 229940057995 liquid paraffin Drugs 0.000 description 2
- 230000014759 maintenance of location Effects 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 229920000609 methyl cellulose Polymers 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 239000001923 methylcellulose Substances 0.000 description 2
- 235000010981 methylcellulose Nutrition 0.000 description 2
- 239000004200 microcrystalline wax Substances 0.000 description 2
- 235000019808 microcrystalline wax Nutrition 0.000 description 2
- GLDOVTGHNKAZLK-UHFFFAOYSA-N octadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCO GLDOVTGHNKAZLK-UHFFFAOYSA-N 0.000 description 2
- 229920006137 organovinylpolysiloxane Polymers 0.000 description 2
- 235000019271 petrolatum Nutrition 0.000 description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 2
- 230000000379 polymerizing effect Effects 0.000 description 2
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- 229920005573 silicon-containing polymer Polymers 0.000 description 2
- 239000000344 soap Substances 0.000 description 2
- PRAKJMSDJKAYCZ-UHFFFAOYSA-N squalane Chemical compound CC(C)CCCC(C)CCCC(C)CCCCC(C)CCCC(C)CCCC(C)C PRAKJMSDJKAYCZ-UHFFFAOYSA-N 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 125000003944 tolyl group Chemical group 0.000 description 2
- 125000000026 trimethylsilyl group Chemical group [H]C([H])([H])[Si]([*])(C([H])([H])[H])C([H])([H])[H] 0.000 description 2
- QIVRABJQTNPYAI-QFIPXVFZSA-N (2s)-n,n'-dibutyl-2-(dodecanoylamino)pentanediamide Chemical compound CCCCCCCCCCCC(=O)N[C@H](C(=O)NCCCC)CCC(=O)NCCCC QIVRABJQTNPYAI-QFIPXVFZSA-N 0.000 description 1
- ALSTYHKOOCGGFT-KTKRTIGZSA-N (9Z)-octadecen-1-ol Chemical compound CCCCCCCC\C=C/CCCCCCCCO ALSTYHKOOCGGFT-KTKRTIGZSA-N 0.000 description 1
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 1
- 229940058015 1,3-butylene glycol Drugs 0.000 description 1
- OBETXYAYXDNJHR-UHFFFAOYSA-N 2-Ethylhexanoic acid Chemical compound CCCCC(CC)C(O)=O OBETXYAYXDNJHR-UHFFFAOYSA-N 0.000 description 1
- TXBCBTDQIULDIA-UHFFFAOYSA-N 2-[[3-hydroxy-2,2-bis(hydroxymethyl)propoxy]methyl]-2-(hydroxymethyl)propane-1,3-diol Chemical compound OCC(CO)(CO)COCC(CO)(CO)CO TXBCBTDQIULDIA-UHFFFAOYSA-N 0.000 description 1
- BGRXBNZMPMGLQI-UHFFFAOYSA-N 2-octyldodecyl tetradecanoate Chemical compound CCCCCCCCCCCCCC(=O)OCC(CCCCCCCC)CCCCCCCCCC BGRXBNZMPMGLQI-UHFFFAOYSA-N 0.000 description 1
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 1
- HIQIXEFWDLTDED-UHFFFAOYSA-N 4-hydroxy-1-piperidin-4-ylpyrrolidin-2-one Chemical compound O=C1CC(O)CN1C1CCNCC1 HIQIXEFWDLTDED-UHFFFAOYSA-N 0.000 description 1
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 1
- 235000019489 Almond oil Nutrition 0.000 description 1
- 239000005995 Aluminium silicate Substances 0.000 description 1
- 235000021357 Behenic acid Nutrition 0.000 description 1
- UTLJLYMJUCOCSM-UHFFFAOYSA-N C(CCCCCCCCCCCCCCCCC)(=O)O.OC(CCCCCCCCCCC(=O)O)CCCCCC.C(CCCCCCCCCCCCCCCCC)(=O)O.C(CCCCCCCCCCCCCCCCC)(=O)O.OC(CCCCCCCCCCC(=O)O)CCCCCC Chemical compound C(CCCCCCCCCCCCCCCCC)(=O)O.OC(CCCCCCCCCCC(=O)O)CCCCCC.C(CCCCCCCCCCCCCCCCC)(=O)O.C(CCCCCCCCCCCCCCCCC)(=O)O.OC(CCCCCCCCCCC(=O)O)CCCCCC UTLJLYMJUCOCSM-UHFFFAOYSA-N 0.000 description 1
- ZAKOWWREFLAJOT-CEFNRUSXSA-N D-alpha-tocopherylacetate Chemical compound CC(=O)OC1=C(C)C(C)=C2O[C@@](CCC[C@H](C)CCC[C@H](C)CCCC(C)C)(C)CCC2=C1C ZAKOWWREFLAJOT-CEFNRUSXSA-N 0.000 description 1
- XMSXQFUHVRWGNA-UHFFFAOYSA-N Decamethylcyclopentasiloxane Chemical compound C[Si]1(C)O[Si](C)(C)O[Si](C)(C)O[Si](C)(C)O[Si](C)(C)O1 XMSXQFUHVRWGNA-UHFFFAOYSA-N 0.000 description 1
- 229920000663 Hydroxyethyl cellulose Polymers 0.000 description 1
- 229920001479 Hydroxyethyl methyl cellulose Polymers 0.000 description 1
- 229920002153 Hydroxypropyl cellulose Polymers 0.000 description 1
- 239000005639 Lauric acid Substances 0.000 description 1
- 241000772415 Neovison vison Species 0.000 description 1
- 239000004677 Nylon Substances 0.000 description 1
- 239000005642 Oleic acid Substances 0.000 description 1
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 1
- 239000004264 Petrolatum Substances 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 229920002367 Polyisobutene Polymers 0.000 description 1
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 1
- 235000019485 Safflower oil Nutrition 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- 229930006000 Sucrose Natural products 0.000 description 1
- 240000001417 Vigna umbellata Species 0.000 description 1
- 235000011453 Vigna umbellata Nutrition 0.000 description 1
- OWRMXHRUFYLLQP-UHFFFAOYSA-N [3-[2,3-bis(16-methylheptadecanoyloxy)propoxy]-2-hydroxypropyl] 16-methylheptadecanoate Chemical compound CC(C)CCCCCCCCCCCCCCC(=O)OCC(O)COCC(OC(=O)CCCCCCCCCCCCCCC(C)C)COC(=O)CCCCCCCCCCCCCCC(C)C OWRMXHRUFYLLQP-UHFFFAOYSA-N 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 238000012644 addition polymerization Methods 0.000 description 1
- 238000007259 addition reaction Methods 0.000 description 1
- 230000001476 alcoholic effect Effects 0.000 description 1
- 235000010443 alginic acid Nutrition 0.000 description 1
- 229920000615 alginic acid Polymers 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 125000003545 alkoxy group Chemical group 0.000 description 1
- 239000008168 almond oil Substances 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 239000010775 animal oil Substances 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 235000006708 antioxidants Nutrition 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 235000021302 avocado oil Nutrition 0.000 description 1
- 239000008163 avocado oil Substances 0.000 description 1
- 230000003796 beauty Effects 0.000 description 1
- 235000013871 bee wax Nutrition 0.000 description 1
- 239000012166 beeswax Substances 0.000 description 1
- 229940116226 behenic acid 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
- 235000019437 butane-1,3-diol Nutrition 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- CJZGTCYPCWQAJB-UHFFFAOYSA-L calcium stearate Chemical compound [Ca+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CJZGTCYPCWQAJB-UHFFFAOYSA-L 0.000 description 1
- 235000013539 calcium stearate Nutrition 0.000 description 1
- 239000008116 calcium stearate Substances 0.000 description 1
- HRBZRZSCMANEHQ-UHFFFAOYSA-L calcium;hexadecanoate Chemical compound [Ca+2].CCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCC([O-])=O HRBZRZSCMANEHQ-UHFFFAOYSA-L 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
- SHZIWNPUGXLXDT-UHFFFAOYSA-N caproic acid ethyl ester Natural products CCCCCC(=O)OCC SHZIWNPUGXLXDT-UHFFFAOYSA-N 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000004203 carnauba wax Substances 0.000 description 1
- 235000013869 carnauba wax Nutrition 0.000 description 1
- 235000010418 carrageenan Nutrition 0.000 description 1
- 239000000679 carrageenan Substances 0.000 description 1
- 229920001525 carrageenan Polymers 0.000 description 1
- 229940113118 carrageenan Drugs 0.000 description 1
- 229960001777 castor oil Drugs 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 239000012185 ceresin wax Substances 0.000 description 1
- 229960000541 cetyl alcohol Drugs 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 238000007796 conventional method Methods 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
- ZAKOWWREFLAJOT-UHFFFAOYSA-N d-alpha-Tocopheryl acetate Natural products CC(=O)OC1=C(C)C(C)=C2OC(CCCC(C)CCCC(C)CCCC(C)C)(C)CCC2=C1C ZAKOWWREFLAJOT-UHFFFAOYSA-N 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 230000018044 dehydration Effects 0.000 description 1
- 238000006297 dehydration reaction Methods 0.000 description 1
- GUJOJGAPFQRJSV-UHFFFAOYSA-N dialuminum;dioxosilane;oxygen(2-);hydrate Chemical class O.[O-2].[O-2].[O-2].[Al+3].[Al+3].O=[Si]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O GUJOJGAPFQRJSV-UHFFFAOYSA-N 0.000 description 1
- 229940105990 diglycerin Drugs 0.000 description 1
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 1
- SZXQTJUDPRGNJN-UHFFFAOYSA-N dipropylene glycol Chemical compound OCCCOCCCO SZXQTJUDPRGNJN-UHFFFAOYSA-N 0.000 description 1
- KPUWHANPEXNPJT-UHFFFAOYSA-N disiloxane Chemical class [SiH3]O[SiH3] KPUWHANPEXNPJT-UHFFFAOYSA-N 0.000 description 1
- LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 238000007429 general method Methods 0.000 description 1
- 125000003976 glyceryl group Chemical group [H]C([*])([H])C(O[H])([H])C(O[H])([H])[H] 0.000 description 1
- 125000005843 halogen group Chemical group 0.000 description 1
- IUJAMGNYPWYUPM-UHFFFAOYSA-N hentriacontane Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC IUJAMGNYPWYUPM-UHFFFAOYSA-N 0.000 description 1
- XJNUECKWDBNFJV-UHFFFAOYSA-N hexadecyl 2-ethylhexanoate Chemical compound CCCCCCCCCCCCCCCCOC(=O)C(CC)CCCC XJNUECKWDBNFJV-UHFFFAOYSA-N 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 1
- 239000001863 hydroxypropyl cellulose Substances 0.000 description 1
- 235000010977 hydroxypropyl cellulose Nutrition 0.000 description 1
- 229940072106 hydroxystearate Drugs 0.000 description 1
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
- 229940074928 isopropyl myristate Drugs 0.000 description 1
- XUGNVMKQXJXZCD-UHFFFAOYSA-N isopropyl palmitate Chemical compound CCCCCCCCCCCCCCCC(=O)OC(C)C XUGNVMKQXJXZCD-UHFFFAOYSA-N 0.000 description 1
- 229940075495 isopropyl palmitate Drugs 0.000 description 1
- 229940119170 jojoba wax Drugs 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- 238000004898 kneading Methods 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 239000010445 mica Substances 0.000 description 1
- 229910052618 mica group Inorganic materials 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 239000011259 mixed solution Substances 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- JXTPJDDICSTXJX-UHFFFAOYSA-N n-Triacontane Natural products CCCCCCCCCCCCCCCCCCCCCCCCCCCCCC JXTPJDDICSTXJX-UHFFFAOYSA-N 0.000 description 1
- GOQYKNQRPGWPLP-UHFFFAOYSA-N n-heptadecyl alcohol Natural products CCCCCCCCCCCCCCCCCO GOQYKNQRPGWPLP-UHFFFAOYSA-N 0.000 description 1
- 235000019488 nut oil Nutrition 0.000 description 1
- 239000010466 nut oil Substances 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- HMMGMWAXVFQUOA-UHFFFAOYSA-N octamethylcyclotetrasiloxane Chemical compound C[Si]1(C)O[Si](C)(C)O[Si](C)(C)O[Si](C)(C)O1 HMMGMWAXVFQUOA-UHFFFAOYSA-N 0.000 description 1
- 229940073665 octyldodecyl myristate Drugs 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 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
- 239000004006 olive oil Substances 0.000 description 1
- 235000008390 olive oil Nutrition 0.000 description 1
- 229910052763 palladium Inorganic materials 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
- 229940066842 petrolatum Drugs 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229910052697 platinum Inorganic materials 0.000 description 1
- 150000003058 platinum compounds Chemical class 0.000 description 1
- 239000004584 polyacrylic acid Substances 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 239000002685 polymerization catalyst Substances 0.000 description 1
- 229920001282 polysaccharide Polymers 0.000 description 1
- 239000005017 polysaccharide Substances 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 235000005713 safflower oil Nutrition 0.000 description 1
- 239000003813 safflower oil Substances 0.000 description 1
- 238000007665 sagging Methods 0.000 description 1
- 230000001953 sensory effect Effects 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 238000003892 spreading Methods 0.000 description 1
- 229940032094 squalane Drugs 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 229940012831 stearyl alcohol Drugs 0.000 description 1
- 239000005720 sucrose Substances 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 230000008961 swelling Effects 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- TUNFSRHWOTWDNC-HKGQFRNVSA-N tetradecanoic acid Chemical compound CCCCCCCCCCCCC[14C](O)=O TUNFSRHWOTWDNC-HKGQFRNVSA-N 0.000 description 1
- 229940042585 tocopherol acetate Drugs 0.000 description 1
- 238000011282 treatment Methods 0.000 description 1
- UFTFJSFQGQCHQW-UHFFFAOYSA-N triformin Chemical compound O=COCC(OC=O)COC=O UFTFJSFQGQCHQW-UHFFFAOYSA-N 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 239000000230 xanthan gum Substances 0.000 description 1
- 229920001285 xanthan gum Polymers 0.000 description 1
- 235000010493 xanthan gum Nutrition 0.000 description 1
- 229940082509 xanthan gum Drugs 0.000 description 1
- UHVMMEOXYDMDKI-JKYCWFKZSA-L zinc;1-(5-cyanopyridin-2-yl)-3-[(1s,2s)-2-(6-fluoro-2-hydroxy-3-propanoylphenyl)cyclopropyl]urea;diacetate Chemical compound [Zn+2].CC([O-])=O.CC([O-])=O.CCC(=O)C1=CC=C(F)C([C@H]2[C@H](C2)NC(=O)NC=2N=CC(=CC=2)C#N)=C1O UHVMMEOXYDMDKI-JKYCWFKZSA-L 0.000 description 1
Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野〕
本発明は、油性基剤、シリコーンゲル組成物及び水性基
材を混合してなり、使用感、化粧効果、経時安定性に優
れた油性組成物及びこれを含有する化粧料に関する。Detailed Description of the Invention [Industrial Field of Application] The present invention provides an oil-based composition that is made by mixing an oil-based base, a silicone gel composition, and an aqueous base, and has excellent usability, cosmetic effect, and stability over time. and cosmetics containing the same.
〔従来の技術及び発明が解決しようとする課題〕油性化
粧料は、皮膚に対する付着力、被覆力、化粧膜の耐水性
などの点で優れた特性を有することから、広く使用され
ている。そして従来の油性化粧料は、一般に半固体油も
しくは液体油及び固体油からなる油性基剤、あるいはさ
らに油性ゲル化剤を配合してゲル化させた油性基剤を用
い、これに化粧用粉体を混合、分散させ、固化、成型す
ることにより製造されている。[Prior Art and Problems to be Solved by the Invention] Oil-based cosmetics are widely used because they have excellent properties such as adhesion to the skin, covering power, and water resistance of the cosmetic film. Conventional oil-based cosmetics generally use an oil-based base consisting of semi-solid oil, liquid oil, and solid oil, or an oil-based base that is further blended with an oil-based gelling agent to form a gel. It is manufactured by mixing, dispersing, solidifying, and molding.
しかしながら従来の油性化粧料は油分含有量が多いこと
から、油性タイプ製品特有のべとつき感や油っぽさを感
じる、延び、拡がりが悪い等の欠点があった。However, since conventional oil-based cosmetics have a high oil content, they have the disadvantages of feeling sticky or greasy, which is characteristic of oil-based products, and that they do not spread well.
これらの欠点を解決するため、■水や水性成分を配合し
、分散タイプもしくはW2O型の乳化タイプとする、■
油分量を下げる、■油っぽさの少ない油剤、例えば低粘
度シリコーン油を配合する等が行なわれてきた。In order to solve these drawbacks, we need to: ■ mix water or aqueous ingredients to create a dispersion type or W2O type emulsion type;
Efforts have been made to lower the amount of oil, and to incorporate less oily oils, such as low-viscosity silicone oil.
ところが、水や水性成分等の水性基材を配合した分散タ
イプもしくはW10型乳化タイプの油性化粧料にあって
は、さっばり感を付与することはできるものの、経時的
に水分が揮散したり、同時に油性ゲル化剤として公知の
デキストリン脂肪酸エステル、金属石ケン等を併用して
も経時安定性において問題があった。However, with dispersion type or W10 emulsion type oil-based cosmetics that contain aqueous base materials such as water or aqueous ingredients, although they can give a light feeling, the water evaporates over time, At the same time, even if known dextrin fatty acid esters, metal soaps, etc., which are known as oil-based gelling agents, are used in combination, there are problems in terms of stability over time.
また油分量を下げたり、油っぽさの少ない油剤を配合し
ても油性基剤の有する油っぽさは充分に解消されない。Furthermore, even if the amount of oil is lowered or a less oily agent is added, the oiliness of the oily base cannot be sufficiently eliminated.
特に低粘度シリコーン油は、それ自身ではべたつきが少
なくさっばりした感触を有するにもかかわらず、通常の
油性基剤に配合した場合、さっばり感を付与することが
できず、また油性基剤との相溶性が悪いため化粧料を安
定に維持することが困難であった。In particular, although low-viscosity silicone oil itself has a light feel with little stickiness, when blended with a normal oil base, it cannot impart a light feel, and when mixed with an oil base, it does not have a light feel. It has been difficult to maintain cosmetics stably due to poor compatibility.
従って、油性化粧料の優れた特性を保持しつつ、その欠
点であるべとつき感や油っぽさを感じさせず、さっばり
した使用感を有し、且つ水性基材を安定に保持できる化
粧料が望まれていた。Therefore, a cosmetic that maintains the excellent properties of oil-based cosmetics, does not have the stickiness and oiliness that are their drawbacks, has a light feeling of use, and can stably retain an aqueous base material. was desired.
斯かる実情において、本発明者らは鋭意研究を行なった
結果、油性基剤、架橋構造を有するオルガノポリシロキ
サン重合物と低粘度シリコーン油とからなるシリコーン
ゲル組成物及び水性基材を混合せしめれば、べたつき感
や油っぽさが少なく、さっばりとした使用感を有し、経
時安定性にも優れた油性組成物が得られ、この油性組成
物を含有した化粧料も同様な優れた特性をもつことを見
出し本発明を完成した。Under these circumstances, the inventors of the present invention have conducted extensive research, and as a result, have created a silicone gel composition consisting of an oil base, an organopolysiloxane polymer having a crosslinked structure, and a low viscosity silicone oil, and an aqueous base material. For example, it is possible to obtain an oil-based composition that is less sticky or oily, has a light feeling on use, and has excellent stability over time, and cosmetics containing this oil-based composition also have the same excellent properties. The present invention was completed based on the discovery that the present invention has certain characteristics.
すなわち、本発明は次の成分(八)〜(C)(A)半固
体油もしくは液体油と、固体油及び/または油性ゲル化
剤とを含む油性基剤
(B)部分架橋型オルガノポリシロキサン重合物と、低
粘度シリコーン油とからなるシリコーンゲル組成物
(C)水単独、または水と水溶性高分子、水膨潤性粘土
鉱物もしくは多価アルコールとの肛み合わせから選ばれ
る1種または2種以上の水性基材
からなる油性組成物及びこれを含有する化粧料を提供す
るものである。That is, the present invention comprises the following components (8) to (C) (A) an oily base containing a semi-solid oil or liquid oil, and a solid oil and/or an oily gelling agent; (B) a partially crosslinked organopolysiloxane; Silicone gel composition consisting of a polymer and low viscosity silicone oil (C) One or two selected from water alone, or a combination of water and a water-soluble polymer, a water-swellable clay mineral, or a polyhydric alcohol. The present invention provides an oily composition comprising at least one aqueous base material, and a cosmetic containing the same.
本発明において(A)成分として使用される油性基剤は
、半固体油もしくは液体油に、固体油及び/または油性
ゲル化剤を配合してなるものである。The oil base used as component (A) in the present invention is a semi-solid oil or liquid oil mixed with a solid oil and/or an oil gelling agent.
半固体油または液体油としては、通常化粧品に使用され
るものであれば特に制限されず、鉱物油、植物油、動物
油、高級脂肪酸、高級脂肪酸エステル、高級アルコール
等が使用できる。具体的には、例えば流動パラフィン、
スクヮラン、ヒマシ油、ミリスチン酸イソプロピル、パ
ルミチン酸イソプロピル、ラノリン、ワセリン、オリー
ブ油、ホホバ油、マカデミアンナッツ油、ミンク油、タ
ードル油、アーモンド油、サフラワー油、アボガド油、
ミリスチン酸オクチルドデシル、2−エチルヘキサン酸
セチル、2−エチルへ牛すン酸トリグリセライドなどの
グリセリン脂肪酸エステル、ジグリセリルイソステアレ
ートなどのジグリセリン脂肪酸エステル、シカプリン酸
プロピレングリコールなどのプロピレングリコールfl
it肪酸エステル、ジペンタエリトリット脂肪酸エステ
ル、オレイン酸、オレイルアルコールなどが挙げられる
。The semi-solid oil or liquid oil is not particularly limited as long as it is normally used in cosmetics, and mineral oils, vegetable oils, animal oils, higher fatty acids, higher fatty acid esters, higher alcohols, etc. can be used. Specifically, for example, liquid paraffin,
Squalane, castor oil, isopropyl myristate, isopropyl palmitate, lanolin, petrolatum, olive oil, jojoba oil, macadamian nut oil, mink oil, turdle oil, almond oil, safflower oil, avocado oil,
Glycerin fatty acid esters such as octyldodecyl myristate, cetyl 2-ethylhexanoate, and 2-ethylhexanoate triglyceride, diglycerin fatty acid esters such as diglyceryl isostearate, and propylene glycol fl such as propylene glycol capriate.
Examples include it fatty acid ester, dipentaerythritol fatty acid ester, oleic acid, oleyl alcohol, and the like.
固体油としては、通常化粧品に使用される融点40℃以
上の固体油であれば特に制限されず、炭化水素類、ロウ
類、硬化油、高級脂肪酸、高級アルコール等が使用でき
る。具体的には、例えば固形パラフィンワックス、セレ
シンワックス、マイクロクリスタリンワックス、カルナ
ウバワックス、キャンデリラワックス、ミツロウ、モク
ロウ、ゲイロウ、ポリエチレンワックス、硬化ヒマシ油
、ロジン酸ペンタエリトリットエステル、ステアリン酸
、ラウリン酸、ミリスチン酸、ベヘニン酸、セチルアル
コール、ステアリルアルコール、ラウリルアルコールな
どが挙げられる。The solid oil is not particularly limited as long as it is a solid oil with a melting point of 40° C. or higher that is commonly used in cosmetics, and hydrocarbons, waxes, hydrogenated oils, higher fatty acids, higher alcohols, etc. can be used. Specifically, for example, solid paraffin wax, ceresin wax, microcrystalline wax, carnauba wax, candelilla wax, beeswax, Japanese wax wax, gay wax, polyethylene wax, hydrogenated castor oil, rosin acid pentaerythritol ester, stearic acid, lauric acid. , myristic acid, behenic acid, cetyl alcohol, stearyl alcohol, lauryl alcohol, and the like.
油性ゲル化剤は、前記油成分をゲル化して化才庄料の固
さを調整し、また該化粧料の肌への適度な伸びを得るた
めに配合されるものである。この油性ゲル化剤としては
化粧品分野において公知のものが使用でき、例えば有機
変性モンモリロナイトクレーなどの粘土鉱物;でんぷん
脂肪酸エステル類(例えば平均重合度10〜50のでん
ぷん分解物の脂肪酸エステル):親油性ショ糖脂肪酸エ
ステル類(例えば脂肪酸の炭素数が12以上で、エステ
ル組成はモノエステル力月O重量%以下のもの);ラウ
ロイルグルタミン酸ジブチルアミド、ジラウロイルリジ
ンステアリルアミン塩などのN−アシルアミノ酸のアミ
ド、エステル、アミン塩などの誘導体;I2−ヒドロキ
システアリン酸アルミニウム、ステアリン酸カルシウム
、パルミチン酸カルシウム等の金属石ケン類などが用い
られる。The oil-based gelling agent is blended to gel the oil component to adjust the hardness of the cosmetic agent and to ensure that the cosmetic composition spreads appropriately on the skin. As this oily gelling agent, those known in the cosmetics field can be used, such as clay minerals such as organically modified montmorillonite clay; starch fatty acid esters (for example, fatty acid esters of starch decomposition products with an average degree of polymerization of 10 to 50); lipophilic Sucrose fatty acid esters (for example, those in which the number of carbon atoms in the fatty acid is 12 or more, and the ester composition is less than 0% by weight of monoester); amides of N-acylamino acids such as lauroylglutamic acid dibutylamide and dilauroyllysine stearylamine salt; , esters, amine salts, and other derivatives; metal soaps such as aluminum I2-hydroxystearate, calcium stearate, and calcium palmitate.
これらの固体油、油性ゲル化剤を各々単独で、または二
種以上を組み合わせて前記半固体油または液体油と混合
することにより、本発明に使用される油性基剤とするこ
とができる。固体油及び/または油性ゲル化剤の配合割
合は、特に限定されないが、油性基剤中5〜40重量%
が好ましい。The oily base used in the present invention can be prepared by mixing these solid oils and oily gelling agents alone or in combination with the semisolid oil or liquid oil. The blending ratio of solid oil and/or oily gelling agent is not particularly limited, but is 5 to 40% by weight in the oily base.
is preferred.
また、 ([])成分であるシリコーンゲル組成物は、
(a)部分架橋型オルガノポリシロキサン重合物と、ら
)低粘度シリコーン油とからなるものであり、(a)の
重合物中にCo)のシリコーン油を内包せしめたもので
ある。In addition, the silicone gel composition that is the ([]) component is
It is composed of (a) a partially crosslinked organopolysiloxane polymer and (ra) a low-viscosity silicone oil, and the silicone oil (Co) is encapsulated in the polymer (a).
上記(a)の部分架橋型オルガノポリシロキサン重合物
としては、例えば、オルガノポリシロキサンを架橋結合
させて得られる、ベンゼンに不溶で、自重以上のベンゼ
ンを含み得る三次元架橋構造を一部に有するオルガノポ
リシロキサン重合物が挙げられる。The partially crosslinked organopolysiloxane polymer of (a) above is, for example, obtained by crosslinking organopolysiloxanes and has a three-dimensional crosslinked structure in part that is insoluble in benzene and can contain more than its own weight of benzene. Examples include organopolysiloxane polymers.
該重合物は、R25iO単位及びR31O,、S単位を
有するものであり、R35I00. s単位及び/また
は5lO2単位を含んでいても良い。このものが、ベン
ゼンに不溶であるが、自重以上のベンゼンを含み得る三
次元架橋構造を有する構造をとるためには、R31O,
、、単位及び/またはS10.単位と、R25IO単位
及び/またはR35lO0,、単位との比が適当な範囲
にあることが必要である。R3101,s単位及び/ま
たは5lO7単位が少なすぎると、オルガノポリシロキ
サン重合物は十分な三次元架橋構造とならず、ベンゼン
に可溶となり、たとえ見掛上架橋構造をとっていても使
用できない。また、RzS+O単位及び/またはR35
IOG、 s単位に比して、R3101,s単位及び/
または5lO2単位が多すぎると、オルガノポリシロキ
サンは強固な架橋構造をとり、ベンゼンに不溶ではある
が、重合物の自重量未満しかベンゼンを含むことができ
ないものとなり、低粘度シリコーン油と混和するとオル
ガノポリシロキサン重合物が充分に膨潤せず、シリコー
ン油の分離、排出を生じ、安定維持ができないため使用
できなくなる。このため、ソフトで安定性の良好なシリ
コーンゲル組成物を得るためには、(該重合物の分子量
にも影響されるが)一般には(R2SiO単位及び/ま
たはR=SiOo、 5単位) : (R3iO,
,5単位/または3I02単位)が1:1〜30:1の
範囲内であるものを用いるのが好ましい結果を与える。The polymer has R25iO units and R31O,,S units, and has R35I00. It may contain s units and/or 5lO2 units. In order for this substance to have a three-dimensional crosslinked structure that is insoluble in benzene but can contain more than its own weight of benzene, R31O,
, , units and/or S10. It is necessary that the ratio of the unit to the R25IO unit and/or R35lO0, unit is within an appropriate range. If the R3101,s units and/or 5lO7 units are too small, the organopolysiloxane polymer will not have a sufficient three-dimensional crosslinked structure and will become soluble in benzene, making it unusable even if it has an apparent crosslinked structure. Also, RzS+O unit and/or R35
Compared to IOG, s units, R3101, s units and/or
Alternatively, if there are too many 5lO2 units, the organopolysiloxane will take on a strong crosslinked structure, and although it is insoluble in benzene, it will contain less benzene than its own weight, and when mixed with low viscosity silicone oil, the organopolysiloxane will become The polysiloxane polymer does not swell sufficiently, causing separation and discharge of silicone oil, making it impossible to maintain stability and making it unusable. Therefore, in order to obtain a silicone gel composition that is soft and has good stability, (although it is also influenced by the molecular weight of the polymer) (R2SiO units and/or R=SiOo, 5 units): ( R3iO,
, 5 units/or 3I02 units) within the range of 1:1 to 30:1 gives preferable results.
前記各構造単位において、Rは水素原子;メチル基、エ
チル基、プロピル基等のアルキル基;フェニル基、トリ
ル基等のアリール基;ビニルM’6の脂肪族不飽和基な
どが例示され、同種でも、または異なった種類であって
も良い。In each of the above structural units, R is a hydrogen atom; an alkyl group such as a methyl group, an ethyl group, or a propyl group; an aryl group such as a phenyl group or a tolyl group; an aliphatic unsaturated group such as vinyl M'6; or may be of a different kind.
このような、ベンゼンに不溶であるが、自重以上のベン
ゼンを含み得る三次元架橋構造を有するオルガノポリシ
ロキサン重合物は、例えば次に示すような種々の方法で
合成することができる。Such an organopolysiloxane polymer having a three-dimensional crosslinked structure that is insoluble in benzene but can contain more than its own weight of benzene can be synthesized, for example, by various methods as shown below.
■ 1分子中に少なくとも2個のケイ素原子に結合した
水素原子を有するオルガノハイドロジエンポリシロキサ
ンに、触媒量のアルカリ金属水酸化物のアルコール性水
溶液を加えて加熱し、脱水素反応及び縮合反応を行なう
方法。■ A catalytic amount of an alcoholic aqueous solution of an alkali metal hydroxide is added to an organohydrodiene polysiloxane having at least two silicon-bonded hydrogen atoms in one molecule and heated to cause a dehydrogenation reaction and a condensation reaction. How to do it.
■ 1分子中に少なくとも2個のケイ素原子に結合した
水素原子を有するオルガノハイドロジエンポリシロキサ
ンと、1分子中に少なくとも2個のケイ素原子に結合し
た水酸基を有するオルガノポリシロキサンとを、触媒量
のアルカリ金属水酸化物、白金化合物等の存在下に加熱
し、脱水素縮合反応を行なう方法。■ An organohydrodiene polysiloxane having at least two silicon-bonded hydrogen atoms in one molecule and an organopolysiloxane having at least two silicon-bonded hydroxyl groups in one molecule in a catalytic amount. A method of heating in the presence of an alkali metal hydroxide, platinum compound, etc. to perform a dehydrogenation condensation reaction.
■ 1分子中に少なくとも2個のケイ素原子に結合した
水酸基を有するオルガノポリシロキサンを、触媒量のア
ルカリ金属水酸化物、有機錫化合物等の存在下に加熱し
、脱水縮合反応を行なう方法。(2) A method in which an organopolysiloxane having at least two hydroxyl groups bonded to silicon atoms in one molecule is heated in the presence of a catalytic amount of an alkali metal hydroxide, an organotin compound, etc. to carry out a dehydration condensation reaction.
■ 1分子中に少なくとも2個のケイ素原子に結合した
水酸基を有するオルガノポリシロキサンと、1分子中に
少なくとも2個のケイ素原子に結合したアルコキシル基
を有するオルガノポリシロキサンとを、触媒量のアルカ
リ金属水酸化物、有機金属錫化合物等の存在下に加熱し
、脱アルコール反応を行なう方法。■ An organopolysiloxane having at least two silicon-bonded hydroxyl groups in one molecule and an organopolysiloxane having at least two silicon-bonded alkoxyl groups in one molecule are combined with a catalytic amount of an alkali metal. A method of performing a dealcoholization reaction by heating in the presence of a hydroxide, organometallic tin compound, etc.
これらのいずれの方法にても、ベンゼンに不溶であるが
、自重以上のベンゼンを含み得る三次元架橋構造を有す
るオルガノポリシロキサン重合物を容易に得ることがで
きる。By any of these methods, it is possible to easily obtain an organopolysiloxane polymer having a three-dimensional crosslinked structure that is insoluble in benzene but can contain more than its own weight of benzene.
また(a)の部分架橋型オルガノポリシロキサン重合物
の上記以外の例としては、シリコーン油に不溶ではある
が、十分に膨潤するオルガノポリシロキサン重合物で、
(イ)オルガノハイドロジエンポリシロキサンと (
B)脂肪族不飽和基含有オルガノポリシロキサンを付加
重合させて得られる重合物であり、一部に三次元架橋構
造を有するものが挙げられる。Examples of the partially crosslinked organopolysiloxane polymer (a) other than the above include organopolysiloxane polymers that are insoluble in silicone oil but swell sufficiently;
(a) Organohydrodiene polysiloxane and (
B) A polymer obtained by addition polymerizing an aliphatic unsaturated group-containing organopolysiloxane, some of which have a three-dimensional crosslinked structure.
ここで用いられる (イ)及びく口)のポリシロキサン
の分子構造は、直鎮状、分岐状、環状のいずれであって
もよいが、目的のオルガノポリシロキサン重合物の合成
反応をコントロールするためには、直鎖状であることが
より好ましい。The molecular structure of the polysiloxane (a) and (a) used here may be straight, branched, or cyclic, but in order to control the synthesis reaction of the desired organopolysiloxane polymer, It is more preferable that the chain be linear.
ここで、反応性基である (イ)のオルガノハイドロジ
エンポリシロキサンにおけるケイ素原子に結合した水素
原子及び(B)の脂肪族不飽和基含有オルガノポリシロ
キサンにおける脂肪族不飽和基は、それぞれ1分子中に
少なくとも2個存在することが両者を重合させて得られ
るオルガノポリシロキサン重合物の一部に三次元架橋構
造を形成する上で必須である。Here, each of the hydrogen atom bonded to a silicon atom in the organohydrodiene polysiloxane (A) and the aliphatic unsaturated group in the aliphatic unsaturated group-containing organopolysiloxane (B), which are reactive groups, is one molecule. The presence of at least two of them is essential for forming a three-dimensional crosslinked structure in a part of the organopolysiloxane polymer obtained by polymerizing both.
また、これら反応性基のそれぞれの分子中における位置
は、−船釣には分子鎖内部であるが、分子鎖末端であっ
てもよい。Further, the position of each of these reactive groups in the molecule is within the molecular chain for boat fishing, but may be at the end of the molecular chain.
また、これら反応性基の各々のオルガノポリシロキサン
中に占める含有量は、ソフトで安定性の良好なシリコー
ンゲル組成物を得るためには、その分子構造が直鎖状ま
たは分岐状のものの場合1〜20モル%、また環状のも
のの場合1〜50モル%であるのが好ましい。含有量が
該範囲を超えると硬い重合物となってしまうと共に後述
する低粘度シリコーン油が三次元架橋構造中に内包し難
くなる傾向となり、分離、排出が起こり安定保持できな
くなってしまう。逆に含有量が該範囲に満たないと、シ
リコーンゲル組成物の構造粘性が乏しくなる傾向にある
。In addition, in order to obtain a soft and stable silicone gel composition, the content of each of these reactive groups in the organopolysiloxane should be adjusted to 1 if the molecular structure is linear or branched. It is preferably 20 mol% to 20 mol%, and 1 to 50 mol% in the case of cyclic ones. If the content exceeds this range, it becomes a hard polymer and the low viscosity silicone oil described below tends to be difficult to incorporate into the three-dimensional crosslinked structure, causing separation and discharge, making it impossible to stably maintain it. Conversely, if the content is less than this range, the silicone gel composition tends to have poor structural viscosity.
(イ)のオルガノハイドロジエンポリシロキサンは、H
3iO,、、単位、R31O3,s単位、R11SiO
単位、R25iO単位、R2H3iOo、 s単位、R
*Si口。。、単位等からなるものである。ここで、R
としては、メチル基、エチル基、プロピル基、ブチル基
などのアルキル基、フェニル基、トリル基などのアリー
ル基、シクロヘキシル基、またはこれらの基の炭素原子
に結合した水素原子の一部または全部をハロゲン原子、
シアノ基などで置換した基などから選択される、ビニル
基などの脂肪族不飽和基を除く非置換または置換−価炭
化水素基が例示される。(A) The organohydrodiene polysiloxane is H
3iO,, unit, R31O3,s unit, R11SiO
Unit, R25iO unit, R2H3iOo, s unit, R
*Si mouth. . , units, etc. Here, R
Examples include alkyl groups such as methyl, ethyl, propyl and butyl groups, aryl groups such as phenyl and tolyl groups, cyclohexyl groups, or some or all of the hydrogen atoms bonded to the carbon atoms of these groups. halogen atom,
Examples include unsubstituted or substituted-valent hydrocarbon groups, excluding aliphatic unsaturated groups such as vinyl groups, selected from groups substituted with cyano groups and the like.
このようなものの代表的な例としては、(CI+、)、
5iO−1f(Cl13)2SiO士う、(7Cl13
1IS+0〕。Typical examples of such things are (CI+,),
5iO-1f(Cl13)2SiO, (7Cl13
1IS+0].
Si (CI+3) s (但し、p=10〜500、
q=2〜50)の単位を含んでなるメチルハイドロジエ
ンポリシロキサンが挙げられ、好適な材料となる。Si (CI+3) s (however, p=10~500,
Methylhydrodiene polysiloxane containing units of q=2 to 50) is a suitable material.
また、 (B)の脂肪族不飽和基含有オルガノポリシロ
キサンの脂肪族不飽和基としては、ビニル基、アリール
基等が挙げられるが、ビニル基が一般的であり、オルガ
ノビニルポリシロキサンとしては、(CH2=CH)
S i[]1. s単位、R31O,、、単位、R(C
lhCH2)Sin単位、LSiOSin単位(Cfl
=Ct12)Sino、 s単位、R:+5iOo、
s単位等からなるものが挙げられる。ここでRは前記(
イ)の場合と同じ意味を示す。Further, examples of the aliphatic unsaturated group of the aliphatic unsaturated group-containing organopolysiloxane (B) include vinyl groups, aryl groups, etc., but vinyl groups are common, and organovinyl polysiloxanes include: (CH2=CH)
S i[]1. s unit, R31O,,, unit, R(C
lhCH2) Sin unit, LSiOSin unit (Cfl
=Ct12) Sino, s unit, R: +5iOo,
Examples include those consisting of s units. Here, R is the above (
It has the same meaning as in case b).
このようなものの代表的な例としては、(C1l、=C
H) (CH−) 、5iO−1f(CII+) 2s
lOテ1及び−5i(CH,+)、(CH=Cl12)
(但し、r=10〜100)の単位、あるいは(CH
,)、5iO−1壬((:I+3) R31Oすj+
(CII=C112) CI、5tO)i及び−Si
(C1b) 3 (但し、m=10〜500、n=2〜
50)の単位を含んでなるメチルビニルポリシロキサン
が挙げられ、これらは混合物であってもよく、好適な材
料となる。A typical example of this is (C1l,=C
H) (CH-), 5iO-1f (CII+) 2s
lOte1 and -5i (CH, +), (CH=Cl12)
(However, the unit of r = 10 to 100) or (CH
,), 5iO-1 壬((:I+3) R31Osj+
(CII=C112) CI, 5tO)i and -Si
(C1b) 3 (However, m=10~500, n=2~
Examples include methylvinylpolysiloxanes comprising units of 50), which may also be mixtures and are suitable materials.
このような (イ〕のオルガノハイドロジエンポリシロ
キサンと (B)の脂肪族不飽和基含有オルガノポリシ
ロキサンの付加反応は、従来公知の一般的な方法で行え
ばよい。例えば、然るべきオルガノハイドロジエンポリ
シロキサンとオルガノビニルポリシロキサンを、各々の
反応性基であるケイ素原子に結合した水累基とビニル基
のモル比で1/3〜3/1の範囲となるように配合した
のち、白金あるいはパラジウムなどの付加重合触媒を添
加し、加温攪拌することにより容易に目的とするシリコ
ーン油に不溶なオルガノポリシロキサン重合物が得られ
る。特に本付加重合触媒としては、特公昭33−996
9号公報に記載されている塩化白金酸を用いることが好
ましい。Such an addition reaction between the organohydrodiene polysiloxane (A) and the aliphatic unsaturated group-containing organopolysiloxane (B) may be carried out by a conventionally known general method. After blending siloxane and organovinylpolysiloxane so that the molar ratio of water groups bonded to silicon atoms, which are reactive groups, to vinyl groups is in the range of 1/3 to 3/1, platinum or palladium The target organopolysiloxane polymer which is insoluble in silicone oil can be easily obtained by adding an addition polymerization catalyst such as JP-B No. 33-996.
It is preferable to use chloroplatinic acid described in Publication No. 9.
一方(b)の低粘度シリコーン油は、特に限定されるも
のではないが、粘度50cs程度以下のものであれば好
適に使用し得る。これは高粘度になるにつれ、それを多
量に用いた結果として感触的に油っぽさが生じ、使用感
上好ましくない方向となるからである。そして低粘度シ
リコーン油としては、低重合度鎮状のジメチルポリシロ
キサン、メチルフェニルポリシロキサン、環状のオクタ
メチルシクロテトラシロキサン、デカメチルシクロペン
タシロキサン等が例示され、必要に応じてこれらの1種
または2種以上を適宜選択して用いられる。On the other hand, the low-viscosity silicone oil (b) is not particularly limited, but any one having a viscosity of about 50 cs or less can be suitably used. This is because as the viscosity increases, if a large amount is used, it becomes oily to the touch, which is unfavorable in terms of feel. Examples of the low-viscosity silicone oil include dimethylpolysiloxane, methylphenylpolysiloxane, cyclic octamethylcyclotetrasiloxane, and decamethylcyclopentasiloxane with a low degree of polymerization, and one of these or Two or more types are appropriately selected and used.
シリコーンゲル組成物(成分(B))は、以上の如くし
て得られた(a)の部分架橋型オルガノポリシロキサン
重合物と、(b)の低粘度シリコーン油とを充分混練等
し、膨潤させることにより容易に調製することができる
。ここで、(a)と(b)との混合割合は、重量比で5
:95〜30ニア0、好ましくは10:90〜25ニア
5である。部分架橋型オルガノポリシロキサン重合物の
量が少なくなると、流動粘性を帯び良好なゲル構造を維
持できなくなり、逆に多くなると軟らかいゲル組成物が
得難くなる。The silicone gel composition (component (B)) is prepared by thoroughly kneading the partially crosslinked organopolysiloxane polymer (a) obtained as described above and the low-viscosity silicone oil (b), and then swelling. It can be easily prepared by Here, the mixing ratio of (a) and (b) is 5 by weight.
:95-30 near 0, preferably 10:90-25 near 5. If the amount of the partially crosslinked organopolysiloxane polymer is small, it becomes fluid viscous and a good gel structure cannot be maintained, whereas if it is too large, it becomes difficult to obtain a soft gel composition.
本発明において(C)成分として使用される水性基材は
、水単独または水と水溶性高分子、水膨潤性粘土鉱物も
しくは多価アルコールとの組み合せからなるものである
。具体的には、水溶性高分子としでは、カルボキシビニ
ルポリマー等のポリアクリル酸系化合物、デンプン、メ
チルセルロース、ヒドロキシエチルセルロース、ヒドロ
キシプロピルセルロース等のセルロース系化合物、カラ
ギーナン、キサンタンガム、アルギン酸塩等の多糖類系
化合物が挙げられる。水膨潤性粘土鉱物としては、カオ
リン、ベントナイト等が挙げられる。また、多価アルコ
ールとしては、グリセリン、1.3−ブチレングリコー
ル、ジプロピレングリコール、プロピレングリコール等
が挙げられる。The aqueous base material used as component (C) in the present invention is composed of water alone or a combination of water and a water-soluble polymer, a water-swellable clay mineral, or a polyhydric alcohol. Specifically, water-soluble polymers include polyacrylic acid compounds such as carboxyvinyl polymers, cellulose compounds such as starch, methyl cellulose, hydroxyethyl cellulose, and hydroxypropyl cellulose, and polysaccharide compounds such as carrageenan, xanthan gum, and alginates. Examples include compounds. Examples of water-swellable clay minerals include kaolin and bentonite. Further, examples of the polyhydric alcohol include glycerin, 1,3-butylene glycol, dipropylene glycol, propylene glycol, and the like.
ここにおいて、上記水溶性高分子、水膨潤性粘土鉱物ま
たは多価アルコールを水性基材の成分として使用する場
合、各成分の配合比率は以下の範囲であるのが好ましい
。Here, when the above-mentioned water-soluble polymer, water-swellable clay mineral, or polyhydric alcohol is used as a component of the aqueous base material, the blending ratio of each component is preferably within the following range.
水:水溶性高分子=99.9 : 0.1〜90:IQ
水:水膨潤性粘土鉱物=99.5 : 0.5〜80
: 20水:多価アルコール−90:10〜20:80
また、これらの水性基材は、単独で、または2種以上を
組み合わせて使用することができる。Water: Water-soluble polymer = 99.9: 0.1-90: IQ
Water: water-swellable clay mineral = 99.5: 0.5-80
: 20 water: polyhydric alcohol - 90:10 to 20:80
Moreover, these aqueous base materials can be used individually or in combination of 2 or more types.
本発明における油性組成物を構成する(八)の油性基剤
、(B)のシリコーンゲル組成物及び(C)の水性基材
の配合比率は、次に示す範囲内であるのが好ましい。The blending ratio of the oil base (8), the silicone gel composition (B), and the aqueous base (C) that constitute the oil composition of the present invention is preferably within the following range.
成分 好ましい配合量 特に好ましい配合量(八)
20〜90重量% 40〜70重量%(B)5〜7
0重量% 15〜50重量%(C) 0.5〜50
重量% 0.5〜20重量%また、成分(八)と成分
(0)との配合比率は90:10〜25ニア5、成分(
A)と成分(C)との配合比率は99:1〜30ニア0
の範囲であるのが好ましい。Ingredients Preferred amount Particularly preferred amount (8)
20-90% by weight 40-70% by weight (B) 5-7
0% by weight 15-50% by weight (C) 0.5-50
Weight% 0.5-20% by weight In addition, the blending ratio of component (8) and component (0) is 90:10-25 near 5, component (
The blending ratio of A) and component (C) is 99:1 to 30 near 0
It is preferable that it is in the range of .
本発明の油性組成物を製造するには、上記成分(八)〜
(C)、即ち、油性基剤、シリコーンゲル組成物及び水
性基材を常法に従い混合すればよい。In order to produce the oily composition of the present invention, the above components (8) to
(C), that is, the oil base, the silicone gel composition, and the aqueous base may be mixed according to a conventional method.
添加順序は特に限定されないが、混合することにより油
性基剤、シリコーンゲル組成物及び水性基材が安定な状
態となるようにするのが好ましい。Although the order of addition is not particularly limited, it is preferable that the oil base, silicone gel composition, and aqueous base be in a stable state by mixing.
本発明の油性組成物を含有する化粧料としては、クリー
ム、乳液等の基礎化粧料;整髪料等の頭髪化f、i料;
ファンデーション、白粉、はぼ紅、アイシャドウ、口紅
、ネイルトリートメント等のメーキャップ化粧料などが
挙げられる。Cosmetics containing the oil-based composition of the present invention include basic cosmetics such as creams and emulsions; hair styling products such as hair styling products;
Examples include makeup cosmetics such as foundation, white powder, red bean paste, eye shadow, lipstick, and nail treatments.
本発明の化粧料には、前記必須成分の他に本発明の効果
を防げない範囲で香料、防腐剤、紫外線吸収剤、界面活
性剤、酸化防止剤、美容成分、高分子化合物、化粧用粉
体等を製品種や化粧目的に応じて適宜配合することがで
きる。In addition to the above-mentioned essential ingredients, the cosmetic of the present invention may contain fragrances, preservatives, ultraviolet absorbers, surfactants, antioxidants, beauty ingredients, polymer compounds, and cosmetic powders to the extent that they do not prevent the effects of the present invention. The body etc. can be blended as appropriate depending on the product type and cosmetic purpose.
本発明の化粧料は、油性基剤、シリコーンゲル組成物及
び水性基材が混合分散しているものである。The cosmetic of the present invention contains an oil base, a silicone gel composition, and an aqueous base mixed and dispersed therein.
そしてこのシリコーンゲル組成物中に配合されている低
粘度シリコーン油は、部分架橋型オルガノポリシロキサ
ン重合物の三次元架橋構造中にとり込まれて存在してい
る。すなわち、このシリコーンゲル組成物のゲル構造は
、僅かな外力で速やかに破壊されるため、本発明化粧料
使用時の塗布体での擦取、机上での塗布展延により、内
包されていた低粘度シリコーン油が速やかににじみ出て
くる。The low-viscosity silicone oil blended into this silicone gel composition exists incorporated into the three-dimensional crosslinked structure of the partially crosslinked organopolysiloxane polymer. That is, the gel structure of this silicone gel composition is quickly destroyed by a slight external force, so when using the cosmetic of the present invention, the contained silicone gel composition can be removed by rubbing it with the application body or spreading it on a desk. Viscosity silicone oil oozes out quickly.
また、水、水溶性高分子、水膨潤性粘土鉱物及び多価ア
ルコールは、水性基材とし“C1他と混じり合わない滴
状態で存在しているものである。このため水分の揮散が
効果的に抑制されると共に安定に保持され、使用時には
油性メークアップ化粧料で往々に見受けられた重い油感
が解消され、しかも化粧効果が改善される。In addition, water, water-soluble polymers, water-swellable clay minerals, and polyhydric alcohols are aqueous base materials that exist in the form of droplets that do not mix with C1 and others. Therefore, volatilization of water is effective. When used, the heavy oily feel often seen with oil-based makeup cosmetics is eliminated, and the makeup effect is improved.
従って本発明の化mllは、油性タイプの製品特有の付
着力、被覆力、化粧膜の耐水性などの特性を有し、かつ
低粘度シリコーン油が皮膚に直接作用することからべた
つきや油っぽさがなく、なめらかですべり感のある、さ
っばりとした感触を有する。また本発明化粧料は、化粧
膜にあぶらぴかりがなく、自然で仕上り状態が良好であ
り、化粧もちが良い等、化粧効果も良好である。Therefore, the chemical ml of the present invention has characteristics such as adhesion, covering power, and water resistance of a cosmetic film that are unique to oil-based products, and since the low-viscosity silicone oil acts directly on the skin, it does not cause stickiness or oiliness. It has a smooth, slippery, and light feel without any sagging. Moreover, the cosmetic of the present invention has a good cosmetic effect, such as no oily shine on the cosmetic film, a natural and good finish, and good makeup retention.
次に参考例及び実施例を挙げて本発明を説明する。 Next, the present invention will be explained with reference to reference examples and examples.
参考例1
トリメチルシリル末端封鎖ジメチルメチルハイドロジエ
ンポリシロキサン〔分子量2300゜CH,H3iO:
(CH3)=SiO= 1 : 4 (モル比)〕
に11%水酸化カリウム溶液エタノール:水=2:l
(重量比)〕を適量加え、加熱、還流して重合反応を行
ない、反応生成物を得た。次いでこの反応生成物を水洗
浄してアルカリ剤を除去後、自然乾燥させることにより
ベンゼンに不溶であり、ベンゼンを自重の180%含み
得るシリコーン重合物を製造した。Reference Example 1 Trimethylsilyl end-capped dimethylmethylhydrodiene polysiloxane [molecular weight 2300° CH, H3iO:
(CH3)=SiO=1:4 (molar ratio)]
11% potassium hydroxide solution ethanol:water = 2:l
(weight ratio)] was added, and a polymerization reaction was carried out by heating and refluxing to obtain a reaction product. Next, this reaction product was washed with water to remove the alkaline agent, and then air-dried to produce a silicone polymer that is insoluble in benzene and can contain 180% of its weight in benzene.
このシリコーン重合物2重量部とジメチルポリシロキサ
ン(粘度5cs)8重量部とを分散混合後、三本ロール
により充分混練し、膨潤させてシリコーンゲル組成物を
作成した。2 parts by weight of this silicone polymer and 8 parts by weight of dimethylpolysiloxane (viscosity: 5 cs) were dispersed and mixed, thoroughly kneaded using three rolls, and swollen to prepare a silicone gel composition.
参考例2
内容積約51のプラネタリ−ミキサーに、トリメチルシ
リル末端封鎖ジメチルメチルハイドロジエンポリシロキ
サン(平均分子fi2340.5i−f14.5モル%
) 1790g、及びジメチルビニルシリル末端封鎖
ジメチルポリシロキサン(平均分子量930、ビニル基
7.7モル%)7]、Ogを投入し、攪拌混合した。Reference Example 2 In a planetary mixer having an internal volume of about 51 cm, a trimethylsilyl end-capped dimethyl methylhydrodiene polysiloxane (average molecular fi2340.5i-f14.5 mol%
), dimethylvinylsilyl end-capped dimethylpolysiloxane (average molecular weight 930, vinyl group 7.7 mol%) 7], and Og were added and mixed with stirring.
同混合溶液に、塩化白金酸の2%イソプロピルアルコー
ル溶液の0.5g添加を行ない、70〜80℃に昇温し
、2時間攪拌を続けた。その後、系内を5〜IOmmH
gに減圧し、ス) Uッピングを30分間続行した。こ
の結果得られたオルガノポリシロキサン重合物は、無色
の柔軟性を有する固形物であった。To the same mixed solution, 0.5 g of a 2% isopropyl alcohol solution of chloroplatinic acid was added, the temperature was raised to 70 to 80°C, and stirring was continued for 2 hours. After that, the inside of the system was adjusted to 5~IOmmH.
The pressure was reduced to 1.g, and the Upping was continued for 30 minutes. The resulting organopolysiloxane polymer was a colorless, flexible solid.
このオルガノポリシロキサン重合物25重量部とジメチ
ルポリシロキサン(粘度6cs)75重量部とを分散混
合後、三本ロールにより充分混練し、膨潤させてシリコ
ーンゲル組成物を作成した。After dispersing and mixing 25 parts by weight of this organopolysiloxane polymer and 75 parts by weight of dimethylpolysiloxane (viscosity: 6 cs), the mixture was thoroughly kneaded using a triple roll and swelled to prepare a silicone gel composition.
実施例1
ペースト状ファンデーション:
表1に示す組成のペースト状ファンデーションを、下記
製法により調製した。Example 1 Paste-like foundation: A paste-like foundation having the composition shown in Table 1 was prepared by the following manufacturing method.
(製法) 工程A二成分(1)〜(3)を混合加熱溶解。(Manufacturing method) Step A Two components (1) to (3) are mixed and heated and dissolved.
〃 B:成分(6)〜OI)を混合溶解。B: Mix and dissolve components (6) to OI).
//C’成分0の〜00を均一混合後、粉砕。// C' Component 0 to 00 are mixed uniformly and then ground.
D=上記工程八へCで得た各混合物と(4)又は(5)
を三本ロールミルにて均一に混和した後、加熱溶融し次
いで容器に流し
込み、冷却固化してペースト状ファン
デーションを得る。D = each mixture obtained in step C to step 8 above and (4) or (5)
The mixture is uniformly mixed in a three-roll mill, heated and melted, then poured into a container, cooled and solidified to obtain a paste-like foundation.
以下余白
(官能評価)
得られたペースト状ファンデーションの製造直後のもの
、及び密閉チューブ容器に充填して1力月放置したもの
の2種について女性パネル20名による使用テストを行
ない評価した。下記の如く各項目に評価点をつけ、さら
に判定した。この結果を表2及び表3に示す。Margins below (sensory evaluation) Two types of the resulting paste-like foundations, one immediately after manufacture and one left in a closed tube container and left for one month, were evaluated by conducting a usage test by 20 female panelists. Evaluation points were assigned to each item as shown below, and further judgments were made. The results are shown in Tables 2 and 3.
評価点
非常に良い 3点
良いまたは普通 2点
悪い 1点
判定
平均点2.5以上 ◎
平均点2,0〜2.5未満 ○
平均点1.5〜2.0未満 △
平均点1.5未満 X
以下余白
以上の結果より、本発明のペースト状ファンデーション
は比較例1または3のものに比べ、塗布時ののびが非常
に軽く、べたつき感、油っぽさがなく、肌へのフィツト
感、しっとり感に殴れた使用感触の良い、更には水分保
持能力等の経時安定性に優れたものであった。Evaluation score very good 3 points good or average 2 points bad 1 point judgment Average score 2.5 or more ◎ Average score 2.0 to less than 2.5 ○ Average score 1.5 to less than 2.0 △ Average score 1.5 Less than It had a moist feel and a good feel when used, and was also excellent in stability over time, such as moisture retention ability.
実施例2
含水油性基剤:
(成分) 重量%(1)
ジペンクエリトリット脂肪酸エステル20.0
(2) ラノリン 10.
0〔3)精製水 20.0(
4)シリコーンゲル組成物
(参考例1で得たもの) 50.0(製法)
A、成分(1)及び(2)を混合する。Example 2 Water-containing oily base: (Component) Weight % (1)
Dipene querite fatty acid ester 20.0 (2) Lanolin 10.
0 [3) Purified water 20.0 (
4) Silicone gel composition (obtained in Reference Example 1) 50.0 (Production method) Mix A, components (1) and (2).
B、 Aに成分〔3〕を徐々に加えて強攪拌する。B. Gradually add component [3] to A and stir vigorously.
C,Bに〔4〕を加えて混合する。Add [4] to C and B and mix.
実施例3
はぼ紅:
(成分) 重量%(1〕
デキストリン脂肪酸エステル 5.7(2)ポ
リイソブチレン 9.7(3)トリイソ
オクタン酸グリセリ°ル 2.0(4)流動パラフィ
ン 26.6(5) シリコーンゲル
組成物
(参考例1で得たもの> 25.0(6)メチ
ルセルロース 0.1(7)精製水
9.9(8)ナイロン粉末
3.0(9)マイカ
残量OQ 着色顔料
6.200 香料
0.1(製法)
A、成分(1)〜(4)を混合加熱溶解する。Example 3 Habo Beni: (Ingredients) Weight % (1)
Dextrin fatty acid ester 5.7 (2) Polyisobutylene 9.7 (3) Glyceryl triisooctoate 2.0 (4) Liquid paraffin 26.6 (5) Silicone gel composition (obtained in Reference Example 1) 25.0 (6) Methyl cellulose 0.1 (7) Purified water
9.9(8) Nylon powder
3.0(9) Mica
Remaining amount OQ Coloring pigment
6.200 Fragrance
0.1 (Production method) A. Mix and heat components (1) to (4) to dissolve.
B、成分(6)〜(7)を混合膨潤する。B. Mix and swell components (6) to (7).
C2成分(8)〜(11を均一混合後、粉砕する。C2 components (8) to (11) are mixed uniformly and then pulverized.
D、ASB及びCを混合後、(5)及び00を添加して
三本ロールミルにて均一に混和した後、加熱溶融し、次
いで容器に流し込み冷却固化してほぼ紅を得た。After mixing D, ASB and C, (5) and 00 were added and mixed uniformly in a three-roll mill, heated and melted, then poured into a container and cooled to solidify to obtain a nearly red color.
実施例4
スティック状アイクリーム:
(成分) 重量%(1)
マイクロクリスタリンワックス
(m、p、 85℃) 12.0(
2) ロジン酸ペンタエリスリトール 8.0(3
) ジペンタエリトリットテトラ12−ヒドロキシス
テアリン酸セスキス
テアリン酸へミロジンエステル 3.5(4)クリセ
リルイソステアレート 13.0(5) 2−エチ
ルヘキサンi七チJl、 6.0(6) シカ
プリン酸プロピレン
グリコール i 0.0(7)ジグ
リセリルイソステアレート 18.0(8) シリコ
ーンゲル組成物
(参考例2で得られたもの> 18.0(9)
ヒドロキシエチルセルロース 0,5αO精製水
残量0D ジグリセリルト
リイソステア
レート 2.00つ ビ
タミンEアセテート 0.5(製法)
ハ、成分(1)〜(7)、Ql)及び0りを混合加熱溶
解する。Example 4 Stick-shaped eye cream: (Ingredients) Weight % (1)
Microcrystalline wax (m, p, 85℃) 12.0 (
2) Pentaerythritol rosinate 8.0 (3
) Dipentaerythritol tetra 12-hydroxystearic acid sesquistearic acid hemirodine ester 3.5 (4) Chryceryl isostearate 13.0 (5) 2-Ethylhexane i Seventy Jl, 6.0 (6) Propylene glycol cicapric acid i 0.0 (7) Diglyceryl isostearate 18.0 (8) Silicone gel composition (obtained in Reference Example 2> 18.0 (9)
Hydroxyethyl cellulose 0,5αO purified water
Remaining amount: 0D Diglyceryl triisostearate: 2.00 Vitamin E acetate: 0.5 (manufacturing method) C. Mix and heat components (1) to (7), Ql), and dissolve.
B、成分(9)及びαOを混合膨潤する。B. Mix and swell component (9) and αO.
C,A、 B及び成分(8)を混合後、三本ロールミ
ルにて均一に混和した後、加熱溶融し、次いで容器に流
し込み冷却固化してスティック状アイクリームを得た。After mixing C, A, B and component (8), they were uniformly mixed in a three-roll mill, heated and melted, and then poured into a container and cooled to solidify to obtain a stick-shaped eye cream.
以上that's all
Claims (1)
油性ゲル化剤とを含む油性基剤 (B)部分架橋型オルガノポリシロキサン重合物と、低
粘度シリコーン油とからなるシリコーンゲル組成物 (C)水単独、または水と水溶性高分子、水膨潤性粘土
鉱物もしくは多価アルコールとの組み合わせから選ばれ
る1種または2種以上の水性基材 からなる油性組成物。 2、請求項1記載の油性組成物を含有する化粧料。[Claims] 1. The following components (A) to (C) (A) an oily base containing a semi-solid oil or liquid oil and a solid oil and/or an oily gelling agent (B) a partially crosslinked type Silicone gel composition consisting of an organopolysiloxane polymer and a low-viscosity silicone oil (C) One type selected from water alone, or a combination of water and a water-soluble polymer, a water-swellable clay mineral, or a polyhydric alcohol. An oily composition comprising two or more types of aqueous base materials. 2. A cosmetic containing the oily composition according to claim 1.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1253539A JP2796856B2 (en) | 1989-09-28 | 1989-09-28 | Oily cosmetics |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1253539A JP2796856B2 (en) | 1989-09-28 | 1989-09-28 | Oily cosmetics |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH03115207A true JPH03115207A (en) | 1991-05-16 |
JP2796856B2 JP2796856B2 (en) | 1998-09-10 |
Family
ID=17252778
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP1253539A Expired - Lifetime JP2796856B2 (en) | 1989-09-28 | 1989-09-28 | Oily cosmetics |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP2796856B2 (en) |
Cited By (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH05178734A (en) * | 1991-12-27 | 1993-07-20 | Kose Corp | Solid-like water-in-oil type emulsified cosmetic |
JPH1121224A (en) * | 1997-07-04 | 1999-01-26 | Nippon Shikizai Kogyo Kenkyusho:Kk | Cosmetic material |
JPH11228346A (en) * | 1998-02-12 | 1999-08-24 | Kose Corp | Cosmetic |
JP2001278731A (en) * | 2000-03-30 | 2001-10-10 | Kose Corp | Cosmetic |
JP2003160435A (en) * | 2001-11-21 | 2003-06-03 | Pola Chem Ind Inc | Gel composition |
WO2006120876A1 (en) * | 2005-05-02 | 2006-11-16 | Kose Corporation | Makeup cosmetic |
WO2009087849A1 (en) * | 2008-01-07 | 2009-07-16 | Shiseido Company, Ltd. | Makeup remover and device for makeup removal |
JP2009256235A (en) * | 2008-04-16 | 2009-11-05 | Kao Corp | Gel-form cosmetic |
JP2012072000A (en) * | 2010-09-28 | 2012-04-12 | Lion Corp | Method of manufacturing clay mineral dispersion liquid |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP7014229B2 (en) | 2017-10-27 | 2022-02-15 | 信越化学工業株式会社 | Oil-in-water emulsified composition, its manufacturing method, and cosmetics |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6166752A (en) * | 1984-09-11 | 1986-04-05 | Shiseido Co Ltd | Gel composition containing silicone oil |
JPS61113646A (en) * | 1984-11-08 | 1986-05-31 | Shiseido Co Ltd | Gel composition containing silicone oil |
JPS63152308A (en) * | 1986-08-23 | 1988-06-24 | Kobayashi Kooc:Kk | Silicon gel composition and cosmetic containing said composition |
JPH01207354A (en) * | 1987-10-15 | 1989-08-21 | Kobayashi Kose Co Ltd | Silicone gel composition and cosmetic containing said composition |
-
1989
- 1989-09-28 JP JP1253539A patent/JP2796856B2/en not_active Expired - Lifetime
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6166752A (en) * | 1984-09-11 | 1986-04-05 | Shiseido Co Ltd | Gel composition containing silicone oil |
JPS61113646A (en) * | 1984-11-08 | 1986-05-31 | Shiseido Co Ltd | Gel composition containing silicone oil |
JPS63152308A (en) * | 1986-08-23 | 1988-06-24 | Kobayashi Kooc:Kk | Silicon gel composition and cosmetic containing said composition |
JPH01207354A (en) * | 1987-10-15 | 1989-08-21 | Kobayashi Kose Co Ltd | Silicone gel composition and cosmetic containing said composition |
Cited By (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH05178734A (en) * | 1991-12-27 | 1993-07-20 | Kose Corp | Solid-like water-in-oil type emulsified cosmetic |
JPH1121224A (en) * | 1997-07-04 | 1999-01-26 | Nippon Shikizai Kogyo Kenkyusho:Kk | Cosmetic material |
JPH11228346A (en) * | 1998-02-12 | 1999-08-24 | Kose Corp | Cosmetic |
JP2001278731A (en) * | 2000-03-30 | 2001-10-10 | Kose Corp | Cosmetic |
JP2003160435A (en) * | 2001-11-21 | 2003-06-03 | Pola Chem Ind Inc | Gel composition |
WO2006120876A1 (en) * | 2005-05-02 | 2006-11-16 | Kose Corporation | Makeup cosmetic |
JP5085323B2 (en) * | 2005-05-02 | 2012-11-28 | 株式会社コーセー | Makeup cosmetics |
WO2009087849A1 (en) * | 2008-01-07 | 2009-07-16 | Shiseido Company, Ltd. | Makeup remover and device for makeup removal |
JP2009161480A (en) * | 2008-01-07 | 2009-07-23 | Shiseido Co Ltd | Mascara remover product |
JP2009256235A (en) * | 2008-04-16 | 2009-11-05 | Kao Corp | Gel-form cosmetic |
JP2012072000A (en) * | 2010-09-28 | 2012-04-12 | Lion Corp | Method of manufacturing clay mineral dispersion liquid |
Also Published As
Publication number | Publication date |
---|---|
JP2796856B2 (en) | 1998-09-10 |
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