JPH07277923A - Oily cosmetic - Google Patents
Oily cosmeticInfo
- Publication number
- JPH07277923A JPH07277923A JP6087327A JP8732794A JPH07277923A JP H07277923 A JPH07277923 A JP H07277923A JP 6087327 A JP6087327 A JP 6087327A JP 8732794 A JP8732794 A JP 8732794A JP H07277923 A JPH07277923 A JP H07277923A
- Authority
- JP
- Japan
- Prior art keywords
- molecular weight
- average molecular
- polyoxyalkylene
- carbon atoms
- stickiness
- 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.)
- Pending
Links
- 239000002537 cosmetic Substances 0.000 title claims abstract description 29
- 239000007788 liquid Substances 0.000 claims abstract description 12
- 229920001296 polysiloxane Polymers 0.000 claims abstract description 11
- 229920001400 block copolymer Polymers 0.000 claims abstract description 9
- 150000001875 compounds Chemical class 0.000 claims abstract description 8
- HVYWMOMLDIMFJA-DPAQBDIFSA-N cholesterol Chemical compound C1C=C2C[C@@H](O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@H]([C@H](C)CCCC(C)C)[C@@]1(C)CC2 HVYWMOMLDIMFJA-DPAQBDIFSA-N 0.000 claims abstract description 6
- 235000014113 dietary fatty acids Nutrition 0.000 claims abstract description 6
- 239000000194 fatty acid Substances 0.000 claims abstract description 6
- 229930195729 fatty acid Natural products 0.000 claims abstract description 6
- 150000004665 fatty acids Chemical class 0.000 claims abstract description 6
- 150000002148 esters Chemical class 0.000 claims abstract description 5
- -1 polysiloxane Polymers 0.000 claims abstract description 5
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims abstract description 4
- 235000012000 cholesterol Nutrition 0.000 claims abstract description 3
- 238000002156 mixing Methods 0.000 claims abstract description 3
- 125000004432 carbon atom Chemical group C* 0.000 claims description 11
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 5
- 230000000694 effects Effects 0.000 abstract description 14
- 230000002688 persistence Effects 0.000 abstract description 2
- 239000004615 ingredient Substances 0.000 abstract 3
- 150000001298 alcohols Chemical class 0.000 abstract 2
- 229920005684 linear copolymer Polymers 0.000 abstract 1
- 239000002253 acid Substances 0.000 description 11
- 230000000052 comparative effect Effects 0.000 description 10
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 9
- 239000000203 mixture Substances 0.000 description 6
- 125000005456 glyceride group Chemical group 0.000 description 5
- 239000000126 substance Substances 0.000 description 5
- WNWHHMBRJJOGFJ-UHFFFAOYSA-N 16-methylheptadecan-1-ol Chemical compound CC(C)CCCCCCCCCCCCCCCO WNWHHMBRJJOGFJ-UHFFFAOYSA-N 0.000 description 4
- UIVPNOBLHXUKDX-UHFFFAOYSA-N 3,5,5-trimethylhexyl 3,5,5-trimethylhexanoate Chemical compound CC(C)(C)CC(C)CCOC(=O)CC(C)CC(C)(C)C UIVPNOBLHXUKDX-UHFFFAOYSA-N 0.000 description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 3
- ZFMQKOWCDKKBIF-UHFFFAOYSA-N bis(3,5-difluorophenyl)phosphane Chemical compound FC1=CC(F)=CC(PC=2C=C(F)C=C(F)C=2)=C1 ZFMQKOWCDKKBIF-UHFFFAOYSA-N 0.000 description 3
- XDOFQFKRPWOURC-UHFFFAOYSA-N iso-octadecanoic acid Natural products CC(C)CCCCCCCCCCCCCCC(O)=O XDOFQFKRPWOURC-UHFFFAOYSA-N 0.000 description 3
- 229940100554 isononyl isononanoate Drugs 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- 229960003656 ricinoleic acid Drugs 0.000 description 3
- FEUQNCSVHBHROZ-UHFFFAOYSA-N ricinoleic acid Natural products CCCCCCC(O[Si](C)(C)C)CC=CCCCCCCCC(=O)OC FEUQNCSVHBHROZ-UHFFFAOYSA-N 0.000 description 3
- BJRXGOFKVBOFCO-UHFFFAOYSA-N 2-hydroxypropyl 16-methylheptadecanoate Chemical compound CC(C)CCCCCCCCCCCCCCC(=O)OCC(C)O BJRXGOFKVBOFCO-UHFFFAOYSA-N 0.000 description 2
- LEACJMVNYZDSKR-UHFFFAOYSA-N 2-octyldodecan-1-ol Chemical compound CCCCCCCCCCC(CO)CCCCCCCC LEACJMVNYZDSKR-UHFFFAOYSA-N 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 2
- 239000004721 Polyphenylene oxide Substances 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- 238000007796 conventional method Methods 0.000 description 2
- GHVNFZFCNZKVNT-UHFFFAOYSA-N decanoic acid Chemical compound CCCCCCCCCC(O)=O GHVNFZFCNZKVNT-UHFFFAOYSA-N 0.000 description 2
- HQRJTRSKPWEIII-OCANKYAHSA-N icosan-9-yl (z,12r)-12-hydroxyoctadec-9-enoate Chemical compound CCCCCCCCCCCC(CCCCCCCC)OC(=O)CCCCCCC\C=C/C[C@H](O)CCCCCC HQRJTRSKPWEIII-OCANKYAHSA-N 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- WWZKQHOCKIZLMA-UHFFFAOYSA-N octanoic acid Chemical group CCCCCCCC(O)=O WWZKQHOCKIZLMA-UHFFFAOYSA-N 0.000 description 2
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- 239000012188 paraffin wax Substances 0.000 description 2
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 2
- 239000000049 pigment Substances 0.000 description 2
- 229920000570 polyether Polymers 0.000 description 2
- 239000002994 raw material 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
- KDYFGRWQOYBRFD-UHFFFAOYSA-N succinic acid Chemical compound OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 2
- WFXHUBZUIFLWCV-UHFFFAOYSA-N (2,2-dimethyl-3-octanoyloxypropyl) octanoate Chemical compound CCCCCCCC(=O)OCC(C)(C)COC(=O)CCCCCCC WFXHUBZUIFLWCV-UHFFFAOYSA-N 0.000 description 1
- DSEKYWAQQVUQTP-XEWMWGOFSA-N (2r,4r,4as,6as,6as,6br,8ar,12ar,14as,14bs)-2-hydroxy-4,4a,6a,6b,8a,11,11,14a-octamethyl-2,4,5,6,6a,7,8,9,10,12,12a,13,14,14b-tetradecahydro-1h-picen-3-one Chemical compound C([C@H]1[C@]2(C)CC[C@@]34C)C(C)(C)CC[C@]1(C)CC[C@]2(C)[C@H]4CC[C@@]1(C)[C@H]3C[C@@H](O)C(=O)[C@@H]1C DSEKYWAQQVUQTP-XEWMWGOFSA-N 0.000 description 1
- BJDAUCLANVMIOB-UHFFFAOYSA-N (3-decanoyloxy-2,2-dimethylpropyl) decanoate Chemical compound CCCCCCCCCC(=O)OCC(C)(C)COC(=O)CCCCCCCCC BJDAUCLANVMIOB-UHFFFAOYSA-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
- BJEPYKJPYRNKOW-REOHCLBHSA-N (S)-malic acid Chemical compound OC(=O)[C@@H](O)CC(O)=O BJEPYKJPYRNKOW-REOHCLBHSA-N 0.000 description 1
- OVYMWJFNQQOJBU-UHFFFAOYSA-N 1-octanoyloxypropan-2-yl octanoate Chemical compound CCCCCCCC(=O)OCC(C)OC(=O)CCCCCCC OVYMWJFNQQOJBU-UHFFFAOYSA-N 0.000 description 1
- LGEZTMRIZWCDLW-UHFFFAOYSA-N 14-methylpentadecyl octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCCCCCCCCCCCCCC(C)C LGEZTMRIZWCDLW-UHFFFAOYSA-N 0.000 description 1
- NFIHXTUNNGIYRF-UHFFFAOYSA-N 2-decanoyloxypropyl decanoate Chemical compound CCCCCCCCCC(=O)OCC(C)OC(=O)CCCCCCCCC NFIHXTUNNGIYRF-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
- BXCRLBBIZJSWNS-UHFFFAOYSA-N 2-hydroxyethyl hexadecanoate Chemical compound CCCCCCCCCCCCCCCC(=O)OCCO BXCRLBBIZJSWNS-UHFFFAOYSA-N 0.000 description 1
- CBLFQQQLPYAQCP-UHFFFAOYSA-N 2-hydroxyethyl octanoate Chemical compound CCCCCCCC(=O)OCCO CBLFQQQLPYAQCP-UHFFFAOYSA-N 0.000 description 1
- JZSMZIOJUHECHW-GTJZZHROSA-N 2-hydroxypropyl (z,12r)-12-hydroxyoctadec-9-enoate Chemical compound CCCCCC[C@@H](O)C\C=C/CCCCCCCC(=O)OCC(C)O JZSMZIOJUHECHW-GTJZZHROSA-N 0.000 description 1
- LEEDMQGKBNGPDN-UHFFFAOYSA-N 2-methylnonadecane Chemical compound CCCCCCCCCCCCCCCCCC(C)C LEEDMQGKBNGPDN-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
- NRRPJRVSNIJDAP-UHFFFAOYSA-N 2-tetradecanoyloxypropyl tetradecanoate Chemical compound CCCCCCCCCCCCCC(=O)OCC(C)OC(=O)CCCCCCCCCCCCC NRRPJRVSNIJDAP-UHFFFAOYSA-N 0.000 description 1
- 241001237961 Amanita rubescens Species 0.000 description 1
- 239000005632 Capric acid (CAS 334-48-5) Substances 0.000 description 1
- 239000005635 Caprylic acid (CAS 124-07-2) Substances 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 239000004677 Nylon Substances 0.000 description 1
- 241000221095 Simmondsia Species 0.000 description 1
- 235000004433 Simmondsia californica Nutrition 0.000 description 1
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
- JBBRZDLNVILTDL-XNTGVSEISA-N [(3s,8s,9s,10r,13r,14s,17r)-10,13-dimethyl-17-[(2r)-6-methylheptan-2-yl]-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1h-cyclopenta[a]phenanthren-3-yl] 16-methylheptadecanoate Chemical compound C([C@@H]12)C[C@]3(C)[C@@H]([C@H](C)CCCC(C)C)CC[C@H]3[C@@H]1CC=C1[C@]2(C)CC[C@H](OC(=O)CCCCCCCCCCCCCCC(C)C)C1 JBBRZDLNVILTDL-XNTGVSEISA-N 0.000 description 1
- 239000001361 adipic acid Substances 0.000 description 1
- 235000011037 adipic acid Nutrition 0.000 description 1
- BJEPYKJPYRNKOW-UHFFFAOYSA-N alpha-hydroxysuccinic acid Natural products OC(=O)C(O)CC(O)=O BJEPYKJPYRNKOW-UHFFFAOYSA-N 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- GFRHRWJBYWRSJE-UHFFFAOYSA-N bis(16-methylheptadecyl) hexanedioate Chemical compound CC(C)CCCCCCCCCCCCCCCOC(=O)CCCCC(=O)OCCCCCCCCCCCCCCCC(C)C GFRHRWJBYWRSJE-UHFFFAOYSA-N 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 229940073724 cholesteryl isostearate Drugs 0.000 description 1
- 229940125904 compound 1 Drugs 0.000 description 1
- 229940125782 compound 2 Drugs 0.000 description 1
- 125000002704 decyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- SASYSVUEVMOWPL-NXVVXOECSA-N decyl oleate Chemical compound CCCCCCCCCCOC(=O)CCCCCCC\C=C/CCCCCCCC SASYSVUEVMOWPL-NXVVXOECSA-N 0.000 description 1
- 229940105990 diglycerin Drugs 0.000 description 1
- GPLRAVKSCUXZTP-UHFFFAOYSA-N diglycerol Chemical compound OCC(O)COCC(O)CO GPLRAVKSCUXZTP-UHFFFAOYSA-N 0.000 description 1
- KWABLUYIOFEZOY-UHFFFAOYSA-N dioctyl butanedioate Chemical compound CCCCCCCCOC(=O)CCC(=O)OCCCCCCCC KWABLUYIOFEZOY-UHFFFAOYSA-N 0.000 description 1
- 239000002552 dosage form Substances 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 239000003205 fragrance Substances 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- 125000003187 heptyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- DWMMZQMXUWUJME-UHFFFAOYSA-N hexadecyl octanoate Chemical compound CCCCCCCCCCCCCCCCOC(=O)CCCCCCC DWMMZQMXUWUJME-UHFFFAOYSA-N 0.000 description 1
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- VLHZUYUOEGBBJB-UHFFFAOYSA-N hydroxy stearic acid Natural products OCCCCCCCCCCCCCCCCCC(O)=O VLHZUYUOEGBBJB-UHFFFAOYSA-N 0.000 description 1
- VJVOFLWZDWLHNR-MRCUWXFGSA-N icosan-9-yl (z)-docos-13-enoate Chemical compound CCCCCCCCCCCC(CCCCCCCC)OC(=O)CCCCCCCCCCC\C=C/CCCCCCCC VJVOFLWZDWLHNR-MRCUWXFGSA-N 0.000 description 1
- 229940078545 isocetyl stearate 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
- 239000007934 lip balm Substances 0.000 description 1
- 229940057995 liquid paraffin Drugs 0.000 description 1
- 239000001630 malic acid Substances 0.000 description 1
- 235000011090 malic acid Nutrition 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000010445 mica Substances 0.000 description 1
- 229910052618 mica group Inorganic materials 0.000 description 1
- 229940078812 myristyl myristate Drugs 0.000 description 1
- JXTPJDDICSTXJX-UHFFFAOYSA-N n-Triacontane Natural products CCCCCCCCCCCCCCCCCCCCCCCCCCCCCC JXTPJDDICSTXJX-UHFFFAOYSA-N 0.000 description 1
- SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 1
- FBUKVWPVBMHYJY-UHFFFAOYSA-N nonanoic acid Chemical compound CCCCCCCCC(O)=O FBUKVWPVBMHYJY-UHFFFAOYSA-N 0.000 description 1
- 125000001400 nonyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- 229940073665 octyldodecyl myristate Drugs 0.000 description 1
- BARWIPMJPCRCTP-UHFFFAOYSA-N oleic acid oleyl ester Natural products CCCCCCCCC=CCCCCCCCCOC(=O)CCCCCCCC=CCCCCCCCC BARWIPMJPCRCTP-UHFFFAOYSA-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
- BARWIPMJPCRCTP-CLFAGFIQSA-N oleyl oleate Chemical compound CCCCCCCC\C=C/CCCCCCCCOC(=O)CCCCCCC\C=C/CCCCCCCC BARWIPMJPCRCTP-CLFAGFIQSA-N 0.000 description 1
- 235000011837 pasties Nutrition 0.000 description 1
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 229940116422 propylene glycol dicaprate Drugs 0.000 description 1
- WBHHMMIMDMUBKC-XLNAKTSKSA-N ricinelaidic acid Chemical compound CCCCCC[C@@H](O)C\C=C\CCCCCCCC(O)=O WBHHMMIMDMUBKC-XLNAKTSKSA-N 0.000 description 1
- 229920002545 silicone oil Polymers 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 229940032094 squalane Drugs 0.000 description 1
- 239000001384 succinic acid Substances 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- DZKXJUASMGQEMA-UHFFFAOYSA-N tetradecyl tetradecanoate Chemical compound CCCCCCCCCCCCCCOC(=O)CCCCCCCCCCCCC DZKXJUASMGQEMA-UHFFFAOYSA-N 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- PHYFQTYBJUILEZ-IUPFWZBJSA-N triolein Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OCC(OC(=O)CCCCCCC\C=C/CCCCCCCC)COC(=O)CCCCCCC\C=C/CCCCCCCC PHYFQTYBJUILEZ-IUPFWZBJSA-N 0.000 description 1
- 229940099259 vaseline Drugs 0.000 description 1
Landscapes
- Cosmetics (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Abstract
Description
【0001】[0001]
【産業上の利用分野】本発明は、製造方法が簡単で油性
化粧料特有の密着性を向上し、べたつきを軽減し、化粧
効果の持続性に優れる油性化粧料に関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to an oily cosmetic which is easy to produce, has improved adhesion characteristic of oily cosmetics, reduces stickiness, and has excellent durability of cosmetic effects.
【0002】[0002]
【従来の技術】一般に油性化粧料は肌への密着性に優れ
その持続性も良いが、使用時の油性感が強く、べたつき
や異和感を覚えやすい。それ故、従来は比較的べたつき
の少ないシリコーン油や流動パラフィン等を配合し油性
感の軽減をしていた。しかしこの方法では確かにべたつ
きは減少するものの、油性化粧料の最大の特徴である密
着性の良さも減少してしまうため、あまり好ましくなく
その配合バランスをとることもかなり困難である。これ
を改善するため、ポリオキシアルキレンブロックを側鎖
にもつペンダント型ポリエーテル変性シリコーンと液状
の極性油とを併用することが提案(特願平6−4501
1号)されている。2. Description of the Related Art Generally, oil-based cosmetics have excellent adhesion to the skin and good durability, but they have a strong oily feel when used, and are easy to feel sticky or strange. Therefore, conventionally, silicone oil or liquid paraffin, which is relatively less sticky, is blended to reduce the oily feeling. However, although this method surely reduces stickiness, it also reduces the good adhesiveness, which is the greatest feature of oil-based cosmetics, and is not so preferable, and it is quite difficult to balance the composition. In order to improve this, it is proposed to use a pendant type polyether modified silicone having a polyoxyalkylene block as a side chain and a liquid polar oil (Japanese Patent Application No. 6-4501).
No. 1) has been done.
【0003】[0003]
【発明が解決しようとする課題】しかしながら、上記提
案においても、べたつき改善の点でやや不満足であり、
また、併用される液状の極性油の1価アルコールは炭素
数16以上であるが、炭素数16ではべたつきがやや感
じられ、さらに改良することが望まれていた。したがっ
て、本発明は、改善された、油性化粧料特有の密着性を
向上し、べたつきを軽減し、化粧効果の持続性に優れる
油性化粧料を提供することを目的としている。However, even in the above proposal, there is some dissatisfaction in terms of tackiness improvement.
Further, the monohydric alcohol of the liquid polar oil used in combination has 16 or more carbon atoms, but with 16 carbon atoms, some stickiness is felt, and further improvement is desired. Therefore, it is an object of the present invention to provide an improved oil-based cosmetic composition having improved adhesiveness peculiar to the oil-based cosmetic composition, reduced stickiness, and excellent durability of the cosmetic effect.
【0004】[0004]
【課題を解決するための手段】本発明者らは、前記課題
を解決するため鋭意検討した結果、本発明に到達した。
すなわち、一般式化2で表される直鎖状ブロック共重合
体であるポリエーテル変性シリコーンと、20℃におけ
る外観が液状である極性油の少なくとも1種以上含有す
ることを特徴とする油性化粧料である。The present inventors have arrived at the present invention as a result of extensive studies to solve the above problems.
That is, an oily cosmetic comprising at least one of polyether modified silicone which is a linear block copolymer represented by the general formula 2 and polar oil which has a liquid appearance at 20 ° C. Is.
【0005】[0005]
【化2】 [Chemical 2]
【0006】(但し、R1 〜R4 は同一または異種の炭
素数1〜32のアルキル基、x、yは1〜8の整数、
a、bはポリオキシアルキレンの平均分子量を300〜
10,000とする整数であり分子中のポリオキシアル
キレン基を10〜90重量%とする数を示し、mはポリ
シロキサンブロックの平均分子量が400〜10,00
0とする整数、nは少なくとも4の整数であり、そして
直鎖状ブロック共重合体は少なくとも3000の平均分
子量を有する。)(Wherein R 1 to R 4 are the same or different alkyl groups having 1 to 32 carbon atoms, x and y are integers of 1 to 8,
a and b are polyoxyalkylene having an average molecular weight of 300 to
It is an integer of 10,000 and represents the number of polyoxyalkylene groups in the molecule of 10 to 90% by weight, and m represents an average molecular weight of the polysiloxane block of 400 to 10,000.
An integer of 0, n is an integer of at least 4, and the linear block copolymer has an average molecular weight of at least 3000. )
【0007】本発明の前記一般式化2のアルキル基には
メチル基、エチル基、プロピル基、ペンチル基、ヘキシ
ル基、ヘプチル基、オクチル基、ノニル基、デシル基等
が挙げられ、べたつき軽減の上から、好ましくはメチル
基が挙げられる。Examples of the alkyl group represented by the general formula 2 of the present invention include a methyl group, an ethyl group, a propyl group, a pentyl group, a hexyl group, a heptyl group, an octyl group, a nonyl group and a decyl group, which reduce stickiness. From the above, a methyl group is preferable.
【0008】本発明の前記一般式化2で表される、直鎖
状ブロック共重合体であるポリエーテル変性シリコーン
は公知の物質(特開平4−234307号公報)であ
り、該公報では直鎖状ブロック共重合体を配合した皮膚
化粧料を提案しているが、油性化粧料としてはべたつき
と化粧効果の持続性の点では不満足であり、本発明者ら
はその配合について鋭意検討した結果本発明を完成し
た。すなわち、直鎖状ブロック共重合体であるポリエー
テル変性シリコーンと、特定の液状極性油とを配合する
ことによって、初めて油性化粧料特有の密着性を相乗的
に向上し、べたつきをも相乗的に軽減した優れた油性化
粧料を見出したのである。その直鎖状ブロック共重合体
であるポリエーテル変性シリコーン配合量は、油性化粧
料特有の密着性を向上し、べたつきを軽減し、化粧効果
の持続性に優れる範囲を検討した結果、製剤総量を基準
として、1.0〜50.0重量%が好ましい。The polyether-modified silicone, which is a linear block copolymer represented by the general formula 2 of the present invention, is a known substance (Japanese Patent Laid-Open No. 234307/1992), and in this publication, a linear chain is used. Although a skin cosmetic containing a block-shaped block copolymer has been proposed, it is unsatisfactory as an oily cosmetic in terms of stickiness and persistence of the cosmetic effect, and the present inventors have made diligent studies on its combination. Completed the invention. That is, by blending a polyether-modified silicone, which is a linear block copolymer, and a specific liquid polar oil, synergistically improved the adhesiveness peculiar to oily cosmetics and synergistically the stickiness. They have found a reduced and excellent oily cosmetic. The amount of the polyether-modified silicone compound that is the linear block copolymer is improved by improving the adhesiveness peculiar to oily cosmetics, reducing stickiness, and examining the range of excellent durability of the cosmetic effect. As a standard, 1.0 to 50.0% by weight is preferable.
【0009】本発明の液状の極性油は、20℃における
外観が液状のもので、水酸基および/またはエステル結
合を含む化合物である。この極性油の好適な配合量は、
前述と同様の理由から、製剤総量を基準として、3.0
〜50.0重量%が好ましい。The liquid polar oil of the present invention has a liquid appearance at 20 ° C. and is a compound containing a hydroxyl group and / or an ester bond. The suitable amount of this polar oil is
For the same reason as above, 3.0
~ 50.0% by weight is preferred.
【0010】本発明に用いられる、炭素数18以上の1
価アルコールは公知の物質で、たとえば、2−オクチル
ドデカノール、イソステアリルアルコール、オレイルア
ルコール、2−ヘキシルデカノール、ホホバアルコール
等があるが、密着性・べたつき・持続性等の効果に優れ
ている点から、好ましくは2−オクチルドデカノールま
たはイソステアリルアルコールが挙げられる。1 having 18 or more carbon atoms used in the present invention
The polyhydric alcohol is a known substance, for example, 2-octyldodecanol, isostearyl alcohol, oleyl alcohol, 2-hexyldecanol, jojoba alcohol and the like, but they are excellent in the effects of adhesion, stickiness and durability. And preferably 2-octyldodecanol or isostearyl alcohol.
【0011】また、本発明に用いられる他の液状の極性
油は、炭素数3以上の1価アルコール、またはコレステ
ロールと炭素数8以上の脂肪酸、アジピン酸、オキシス
テアリン酸、コハク酸またはリンゴ酸とのエステルであ
りこれらは公知の物質で、たとえば、アジピン酸ジイソ
ステアリル、アジピン酸ジオクチル、イソステアリン酸
ジイソプロピル、イソステアリン酸コレステリル、イソ
ノナン酸イソノニル、エルカ酸オクチルドデシル、オキ
システアリン酸オクチル、オクタン酸セチル、オレイン
酸オクチルドデシル、オレイン酸オレイル、コハク酸ジ
オクチル、ステアリン酸イソセチル、パルミチン酸イソ
プロピル、ミリスチン酸オクチルドデシル、ミリスチン
酸ミリスチル、オレイン酸デシル、リシノレイン酸オク
チルドデシル等があり、前記密着性・べたつき・持続性
等の効果に優れている点から、好ましくはアジピン酸ジ
オクチル、イソノナン酸イソノニル、イソステアリン酸
コレステリルまたはリシノレイン酸オクチルドデシルが
挙げられる。さらに好ましくは、アジピン酸ジオクチ
ル、イソノナン酸イソノニル、リシノレイン酸オクチル
ドデシルが挙げられる。Another liquid polar oil used in the present invention is a monohydric alcohol having 3 or more carbon atoms, or cholesterol and a fatty acid having 8 or more carbon atoms, adipic acid, oxystearic acid, succinic acid or malic acid. These are well-known substances such as diisostearyl adipate, dioctyl adipate, diisopropyl isostearate, cholesteryl isostearate, isononyl isononanoate, octyldodecyl erucate, octyl oxystearate, cetyl octanoate, olein. Octyldodecyl acid, oleyl oleate, dioctyl succinate, isocetyl stearate, isopropyl palmitate, octyldodecyl myristate, myristyl myristate, decyl oleate, octyldodecyl ricinoleate, etc. Ri, from the viewpoint of excellent effects such as the adhesiveness, tackiness, durability, preferably dioctyl adipate, isononyl isononanoate, isostearic acid cholesteryl or ricinoleic acid octyldodecyl. More preferable examples include dioctyl adipate, isononyl isononanoate, and octyldodecyl ricinoleate.
【0012】さらに、本発明に使用する液状極性油とし
ては少なくとも2つ以上の水酸基を有する、エチレング
リコール、プロピレングリコール、ネオペンチルグリコ
ール、グリセリン、ジグリセリン、トリメチロールプロ
パン、ペンタエリスルトールと炭素数7以上の脂肪酸と
のエステルでありこれらは公知の物質で、たとえば、オ
クタン酸エチレングリコール、パルミチン酸エチレング
リコール、イソステアリン酸プロピレングリコール、リ
シノレイン酸プロピレングリコール、ジ(カプリル・カ
プリン酸)プロピレングリコール、ジカプリル酸プロピ
レングリコール、ジミリスチン酸プロピレングリコー
ル、ジカプリン酸プロピレングリコール、ジオクタン酸
ネオペンチルグリコール、ジカプリン酸ネオペンチルグ
リコール、トリイソステアリン酸グリセリド、ジイソス
テアリン酸グリセリド、トリオクタン酸グリセリド、ト
リ(カプリル・カプリン酸)グリセリド、リシノレイン
酸グリセリド、イソステアリン酸ジグリセリド、ジイソ
ステアリン酸ジグリセリド、トリイソステアリン酸ジグ
リセリド、トリオクタン酸トリメチロールプロパン、ト
リイソステアリン酸トリメチロールプロパン、テトラオ
クタン酸ペンタエリスリット等があり、前記密着性・べ
たつき・持続性等の効果に優れている点から、好ましく
はイソステアリン酸プロピレングリコール、ジカプリル
酸プロピレングリコール、リシノレイン酸グリセリドま
たはトリ(カプリル・カプリン酸)グリセリドが挙げら
れる。Further, the liquid polar oil used in the present invention has ethylene glycol, propylene glycol, neopentyl glycol, glycerin, diglycerin, trimethylolpropane, pentaerythritol and carbon number having at least two hydroxyl groups. Esters with 7 or more fatty acids are known substances such as ethylene glycol octanoate, ethylene glycol palmitate, propylene glycol isostearate, propylene glycol ricinoleate, propylene glycol di (capryl / capric acid), dicaprylic acid. Propylene glycol, propylene glycol dimyristate, propylene glycol dicaprate, neopentyl glycol dioctanoate, neopentyl glycol dicaprate, triiso Tearic acid glyceride, diisostearic acid glyceride, trioctanoic acid glyceride, tri (caprylic / capric acid) glyceride, ricinoleic acid glyceride, isostearic acid diglyceride, diisostearic acid diglyceride, triisostearic acid diglyceride, trioctyric acid trimethylolpropane, triisostearic acid trimethylolpropane , Tetraoctanoic acid pentaerythritol and the like, and from the viewpoint of excellent effects such as the above-mentioned adhesion, stickiness and durability, propylene glycol isostearate, propylene glycol dicaprylate, ricinoleic acid glyceride or tri (capryl-caprin) is preferable. Acid) glyceride.
【0013】本発明の油性化粧料には、本発明の目的を
損なわない範囲で前記の必須成分以外にパラフィン、セ
レシン等の固形油性原料、ワセリン、重質流動イソパラ
フィン等のペースト状油性原料、流動パラフィン、スク
ワラン等の液状油性原料、抗酸化剤、防腐剤、香料およ
びタルク、マイカ、酸化チタン、酸化鉄、タール色素、
シルクパウダー、ナイロンパウダー等の粉体顔料を配合
することができる。In the oily cosmetic of the present invention, solid oily raw materials such as paraffin and ceresin, vaseline, pasty oily raw materials such as heavy liquid isoparaffin, and liquid are used in addition to the above-mentioned essential components within the range not impairing the object of the present invention. Liquid oily materials such as paraffin and squalane, antioxidants, preservatives, fragrances and talc, mica, titanium oxide, iron oxide, tar pigments,
Powder pigments such as silk powder and nylon powder can be blended.
【0014】本発明の油性化粧料は、常法に従って、た
とえば口紅、ファンデーション、アイシャドウ、頬紅、
リップクリーム等の剤型に製造し、使用することが可能
である。The oily cosmetic composition of the present invention can be prepared according to a conventional method, for example, lipstick, foundation, eye shadow, blusher,
It can be manufactured and used in a dosage form such as lip balm.
【0015】[0015]
【実施例】以下、実施例により、本発明をさらに説明す
るが、本発明はこれに限定されるものではない。EXAMPLES The present invention will be further described below with reference to examples, but the present invention is not limited thereto.
【0016】実施例1〜2、比較例1(口紅) 表1に、本発明に係わる化合物を配合した実施例および
無配合の比較例を示す。Examples 1 and 2, Comparative Example 1 (lipstick) Table 1 shows an example in which the compound according to the present invention was blended and a comparative example in which it was not blended.
【0017】[0017]
【表1】 [Table 1]
【0018】本発明の化合物1 R1 、R2 、R3 、R4 はCH3 、x、yは4、aは1
8、bは33、nは16.1、mは40であり、分子量
は52,000である。Compound 1 of the present invention R 1 , R 2 , R 3 and R 4 are CH 3 , x and y are 4, and a is 1
8, b is 33, n is 16.1, m is 40, and the molecular weight is 52,000.
【0019】注1:特願平6−45011号の実施例
1。Note 1: Example 1 of Japanese Patent Application No. 6-45011.
【0020】実施例1〜2および比較例1の口紅は通常
の方法で調製をした。これらにつき、テストパネラー2
0名にて実施例試料と比較例試料を唇の左右に均等に塗
布し、べたつき具合の比較を行い、さらに4時間後に化
粧効果の持続性評価を行った。実施例試料において塗布
時のべたつきを訴えたパネラーは皆無であり、4時間後
の化粧効果の持続性も比較例試料に比べ優れていた。The lipsticks of Examples 1 and 2 and Comparative Example 1 were prepared by a usual method. About these, test panel 2
The sample of Example and the sample of Comparative Example were evenly applied to the left and right of the lips by 0 persons, and the stickiness was compared, and after 4 hours, the durability of the cosmetic effect was evaluated. None of the panelists complained of stickiness at the time of application in the sample of the example, and the durability of the cosmetic effect after 4 hours was superior to that of the sample of the comparative example.
【0021】実施例3〜4、比較例2(ファンデーショ
ン)Examples 3 to 4 and Comparative Example 2 (foundation)
【0022】表2に、本発明に係わる化合物を配合した
実施例および無配合の比較例を示す。Table 2 shows examples in which the compound according to the present invention was blended and non-blended comparative examples.
【0023】[0023]
【表2】 [Table 2]
【0024】本発明の化合物2 R1 、R2 、R3 、R4 はCH3 、x、yは4、aは2
0、bは29、nは26.3、mは3であり、分子量は
48,000である。Compound 2 of the present invention R 1 , R 2 , R 3 and R 4 are CH 3 , x and y are 4 and a is 2
0, b is 29, n is 26.3, m is 3, and the molecular weight is 48,000.
【0025】注2:特願平6−45011号の実施例
2。Note 2: Example 2 of Japanese Patent Application No. 6-45011.
【0026】実施例3〜4および比較例2のファンデー
ションは通常の方法で調製をした。これらにつき、テス
トパネラー20名にて実施例試料と比較例試料を顔面の
左右に均等に塗布し、べたつき具合の比較を行い、さら
に3時間後に化粧効果の持続性評価を行った。実施例試
料において塗布時のべたつきを訴えたパネラーは皆無で
あり、3時間後の化粧効果の持続性も比較例試料に比べ
優れていた。The foundations of Examples 3-4 and Comparative Example 2 were prepared by a conventional method. With respect to these, 20 test panelists applied the sample of the example and the sample of the comparative example evenly on the right and left sides of the face, compared the stickiness, and evaluated the durability of the cosmetic effect after 3 hours. None of the panelists complained of stickiness during application in the example sample, and the durability of the cosmetic effect after 3 hours was also superior to that of the comparative sample.
【0027】[0027]
【発明の効果】本発明の油性化粧料は、油性化粧料特有
の密着性を向上し、べたつきを軽減し、化粧効果の持続
性に優れる。EFFECTS OF THE INVENTION The oil-based cosmetic composition of the present invention improves the adhesion characteristic of the oil-based cosmetic composition, reduces stickiness, and is excellent in the durability of the cosmetic effect.
Claims (1)
のアルキル基、x、yは1〜8の整数、a、bはポリオ
キシアルキレンの平均分子量を300〜10,000と
する整数であり分子中のポリオキシアルキレン基を10
〜90重量%とする数を示し、mはポリシロキサンブロ
ックの平均分子量が400〜10,000とする整数、
nは4以上であり、そして直鎖状ブロック共重合体は少
なくとも3000の平均分子量を有する。)で表される
ポリシロキサン・ポリオキシアルキレンブロックを反復
ユニットとする直鎖状ブロック共重合体であるポリエー
テル変性シリコーンと、炭素数18以上の1価アルコー
ル、または炭素数3以上の1価アルコール、コレステロ
ールと炭素数8以上の脂肪酸とのエステル、少なくとも
2つ以上の水酸基を有する化合物と炭素数7以上の脂肪
酸とのエステルの群から選ばれる化合物の一種以上から
なる液状極性油を配合することを特徴とする油性化粧
料。1. A general formula 1 (However, R 1 to R 4 are the same or different and have 1 to 32 carbon atoms.
Is an integer of 1 to 8, a and b are integers having an average molecular weight of polyoxyalkylene of 300 to 10,000, and the number of polyoxyalkylene groups in the molecule is 10
To 90% by weight, m is an integer having an average molecular weight of the polysiloxane block of 400 to 10,000,
n is 4 or greater, and the linear block copolymer has an average molecular weight of at least 3000. ), A polyether-modified silicone that is a linear block copolymer having a repeating unit of polysiloxane / polyoxyalkylene block, and a monohydric alcohol having 18 or more carbon atoms, or a monohydric alcohol having 3 or more carbon atoms. Blending a liquid polar oil comprising one or more compounds selected from the group consisting of an ester of cholesterol and a fatty acid having 8 or more carbon atoms, a compound having at least two hydroxyl groups and an ester of fatty acid having 7 or more carbon atoms. An oily cosmetic characterized by:
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP6087327A JPH07277923A (en) | 1994-04-01 | 1994-04-01 | Oily cosmetic |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP6087327A JPH07277923A (en) | 1994-04-01 | 1994-04-01 | Oily cosmetic |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH07277923A true JPH07277923A (en) | 1995-10-24 |
Family
ID=13911779
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP6087327A Pending JPH07277923A (en) | 1994-04-01 | 1994-04-01 | Oily cosmetic |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH07277923A (en) |
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH08133926A (en) * | 1994-11-10 | 1996-05-28 | Nippon Oil & Fats Co Ltd | Composition for cosmetic |
JP2003160430A (en) * | 2001-11-21 | 2003-06-03 | Noevir Co Ltd | Oil-based cosmetic |
WO2004039347A1 (en) * | 2002-11-01 | 2004-05-13 | Kao Corporation | Liquid skin protective composition |
JP2005089340A (en) * | 2003-09-16 | 2005-04-07 | Dow Corning Toray Silicone Co Ltd | Skin cosmetic |
JP2009528382A (en) * | 2006-03-01 | 2009-08-06 | トリストラータ・インコーポレイテッド | Compositions and methods for topical treatment of tar-responsive skin diseases |
JP2010120914A (en) * | 2008-11-21 | 2010-06-03 | Kao Corp | Sunscreen cosmetic |
JP2011136918A (en) * | 2009-12-26 | 2011-07-14 | Mandom Corp | Skin cosmetic |
JP2011136919A (en) * | 2009-12-26 | 2011-07-14 | Mandom Corp | Skin cosmetic |
-
1994
- 1994-04-01 JP JP6087327A patent/JPH07277923A/en active Pending
Cited By (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH08133926A (en) * | 1994-11-10 | 1996-05-28 | Nippon Oil & Fats Co Ltd | Composition for cosmetic |
JP2003160430A (en) * | 2001-11-21 | 2003-06-03 | Noevir Co Ltd | Oil-based cosmetic |
WO2004039347A1 (en) * | 2002-11-01 | 2004-05-13 | Kao Corporation | Liquid skin protective composition |
JPWO2004039347A1 (en) * | 2002-11-01 | 2006-02-23 | 花王株式会社 | Liquid skin protectant composition |
EP1559415A4 (en) * | 2002-11-01 | 2010-06-23 | Kao Corp | Liquid skin protective composition |
JP2005089340A (en) * | 2003-09-16 | 2005-04-07 | Dow Corning Toray Silicone Co Ltd | Skin cosmetic |
JP2009528382A (en) * | 2006-03-01 | 2009-08-06 | トリストラータ・インコーポレイテッド | Compositions and methods for topical treatment of tar-responsive skin diseases |
JP2010120914A (en) * | 2008-11-21 | 2010-06-03 | Kao Corp | Sunscreen cosmetic |
JP2011136918A (en) * | 2009-12-26 | 2011-07-14 | Mandom Corp | Skin cosmetic |
JP2011136919A (en) * | 2009-12-26 | 2011-07-14 | Mandom Corp | Skin cosmetic |
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