JPH0443043B2 - - Google Patents
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- Publication number
- JPH0443043B2 JPH0443043B2 JP11670383A JP11670383A JPH0443043B2 JP H0443043 B2 JPH0443043 B2 JP H0443043B2 JP 11670383 A JP11670383 A JP 11670383A JP 11670383 A JP11670383 A JP 11670383A JP H0443043 B2 JPH0443043 B2 JP H0443043B2
- Authority
- JP
- Japan
- Prior art keywords
- group
- formula
- agent dispersion
- carbon atoms
- pearl
- 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.)
- Expired
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- 239000003795 chemical substances by application Substances 0.000 claims description 31
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims description 24
- 239000006185 dispersion Substances 0.000 claims description 22
- 125000000217 alkyl group Chemical group 0.000 claims description 16
- 150000002148 esters Chemical class 0.000 claims description 13
- 235000011187 glycerol Nutrition 0.000 claims description 12
- 239000002253 acid Substances 0.000 claims description 11
- 125000004432 carbon atom Chemical group C* 0.000 claims description 11
- -1 polyoxyethylene group Polymers 0.000 claims description 10
- GPLRAVKSCUXZTP-UHFFFAOYSA-N diglycerol Chemical compound OCC(O)COCC(O)CO GPLRAVKSCUXZTP-UHFFFAOYSA-N 0.000 claims description 9
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 9
- 239000003093 cationic surfactant Substances 0.000 claims description 7
- 238000002156 mixing Methods 0.000 claims description 6
- 238000010586 diagram Methods 0.000 claims description 4
- 125000002768 hydroxyalkyl group Chemical group 0.000 claims description 4
- 229930195734 saturated hydrocarbon Natural products 0.000 claims description 4
- 125000005526 alkyl sulfate group Chemical group 0.000 claims description 2
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 2
- 125000005843 halogen group Chemical group 0.000 claims description 2
- 125000001183 hydrocarbyl group Chemical group 0.000 claims description 2
- 229920006395 saturated elastomer Polymers 0.000 claims description 2
- 229930195735 unsaturated hydrocarbon Natural products 0.000 claims description 2
- 239000000203 mixture Substances 0.000 description 14
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 12
- 239000002932 luster Substances 0.000 description 10
- 239000013078 crystal Substances 0.000 description 9
- 239000007788 liquid Substances 0.000 description 9
- 238000000034 method Methods 0.000 description 8
- 235000014113 dietary fatty acids Nutrition 0.000 description 6
- 239000000194 fatty acid Substances 0.000 description 6
- 229930195729 fatty acid Natural products 0.000 description 6
- 238000000926 separation method Methods 0.000 description 6
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 4
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 3
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- 230000005856 abnormality Effects 0.000 description 3
- 238000004220 aggregation Methods 0.000 description 3
- 230000002776 aggregation Effects 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- 238000001816 cooling Methods 0.000 description 3
- 239000011521 glass Substances 0.000 description 3
- 239000004615 ingredient Substances 0.000 description 3
- 239000002667 nucleating agent Substances 0.000 description 3
- 239000002245 particle Substances 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- 229920003169 water-soluble polymer Polymers 0.000 description 3
- PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 description 2
- DMBUODUULYCPAK-UHFFFAOYSA-N 1,3-bis(docosanoyloxy)propan-2-yl docosanoate Chemical group CCCCCCCCCCCCCCCCCCCCCC(=O)OCC(OC(=O)CCCCCCCCCCCCCCCCCCCCC)COC(=O)CCCCCCCCCCCCCCCCCCCCC DMBUODUULYCPAK-UHFFFAOYSA-N 0.000 description 2
- ASKIVFGGGGIGKH-UHFFFAOYSA-N 2,3-dihydroxypropyl 16-methylheptadecanoate Chemical compound CC(C)CCCCCCCCCCCCCCC(=O)OCC(O)CO ASKIVFGGGGIGKH-UHFFFAOYSA-N 0.000 description 2
- UBHGDYHAWJOMOF-UHFFFAOYSA-N 2-[[2-hydroxy-2-(hydroxymethyl)-18-methylnonadecoxy]methyl]-18-methylnonadecane-1,2-diol Chemical compound C(CCCCCCCCCCCCCCC(C)C)C(COCC(O)(CO)CCCCCCCCCCCCCCCC(C)C)(O)CO UBHGDYHAWJOMOF-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 2
- 235000019270 ammonium chloride Nutrition 0.000 description 2
- VBICKXHEKHSIBG-UHFFFAOYSA-N beta-monoglyceryl stearate Natural products CCCCCCCCCCCCCCCCCC(=O)OCC(O)CO VBICKXHEKHSIBG-UHFFFAOYSA-N 0.000 description 2
- WOWHHFRSBJGXCM-UHFFFAOYSA-M cetyltrimethylammonium chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCC[N+](C)(C)C WOWHHFRSBJGXCM-UHFFFAOYSA-M 0.000 description 2
- REZZEXDLIUJMMS-UHFFFAOYSA-M dimethyldioctadecylammonium chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCCCC[N+](C)(C)CCCCCCCCCCCCCCCCCC REZZEXDLIUJMMS-UHFFFAOYSA-M 0.000 description 2
- 239000002612 dispersion medium Substances 0.000 description 2
- 239000004664 distearyldimethylammonium chloride (DHTDMAC) Substances 0.000 description 2
- 150000004665 fatty acids Chemical class 0.000 description 2
- 230000003165 hydrotropic effect Effects 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 239000002453 shampoo Substances 0.000 description 2
- 238000003860 storage Methods 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- QLAJNZSPVITUCQ-UHFFFAOYSA-N 1,3,2-dioxathietane 2,2-dioxide Chemical compound O=S1(=O)OCO1 QLAJNZSPVITUCQ-UHFFFAOYSA-N 0.000 description 1
- 229940058015 1,3-butylene glycol Drugs 0.000 description 1
- SKTISOFAJJJZGA-UHFFFAOYSA-N 1-chloro-2-octadecylicosan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCC(C(O)Cl)CCCCCCCCCCCCCCCCCC SKTISOFAJJJZGA-UHFFFAOYSA-N 0.000 description 1
- RZRNAYUHWVFMIP-KTKRTIGZSA-N 1-oleoylglycerol Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OCC(O)CO RZRNAYUHWVFMIP-KTKRTIGZSA-N 0.000 description 1
- 241000251468 Actinopterygii Species 0.000 description 1
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 1
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 1
- QHZLMUACJMDIAE-UHFFFAOYSA-N Palmitic acid monoglyceride Natural products CCCCCCCCCCCCCCCC(=O)OCC(O)CO QHZLMUACJMDIAE-UHFFFAOYSA-N 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 1
- VBIIFPGSPJYLRR-UHFFFAOYSA-M Stearyltrimethylammonium chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCCCC[N+](C)(C)C VBIIFPGSPJYLRR-UHFFFAOYSA-M 0.000 description 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 1
- 239000012190 activator Substances 0.000 description 1
- OGBUMNBNEWYMNJ-UHFFFAOYSA-N batilol Chemical class CCCCCCCCCCCCCCCCCCOCC(O)CO OGBUMNBNEWYMNJ-UHFFFAOYSA-N 0.000 description 1
- YSJGOMATDFSEED-UHFFFAOYSA-M behentrimonium chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCCCCCCCC[N+](C)(C)C YSJGOMATDFSEED-UHFFFAOYSA-M 0.000 description 1
- FADYGXGJTNYCHZ-UHFFFAOYSA-M benzyl-dodecyl-diethylazanium;chloride Chemical compound [Cl-].CCCCCCCCCCCC[N+](CC)(CC)CC1=CC=CC=C1 FADYGXGJTNYCHZ-UHFFFAOYSA-M 0.000 description 1
- 229940073609 bismuth oxychloride Drugs 0.000 description 1
- 235000019437 butane-1,3-diol Nutrition 0.000 description 1
- KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 150000001990 dicarboxylic acid derivatives Chemical class 0.000 description 1
- 150000005690 diesters Chemical class 0.000 description 1
- PFKRTWCFCOUBHS-UHFFFAOYSA-N dimethyl(octadecyl)azanium;chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCCCC[NH+](C)C PFKRTWCFCOUBHS-UHFFFAOYSA-N 0.000 description 1
- XJWSAJYUBXQQDR-UHFFFAOYSA-M dodecyltrimethylammonium bromide Chemical compound [Br-].CCCCCCCCCCCC[N+](C)(C)C XJWSAJYUBXQQDR-UHFFFAOYSA-M 0.000 description 1
- 235000019441 ethanol Nutrition 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 239000003205 fragrance Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000012456 homogeneous solution Substances 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- 239000011147 inorganic material Substances 0.000 description 1
- 239000006210 lotion Substances 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
- RZRNAYUHWVFMIP-UHFFFAOYSA-N monoelaidin Natural products CCCCCCCCC=CCCCCCCCC(=O)OCC(O)CO RZRNAYUHWVFMIP-UHFFFAOYSA-N 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 235000006408 oxalic acid Nutrition 0.000 description 1
- BWOROQSFKKODDR-UHFFFAOYSA-N oxobismuth;hydrochloride Chemical compound Cl.[Bi]=O BWOROQSFKKODDR-UHFFFAOYSA-N 0.000 description 1
- 238000005191 phase separation Methods 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920001515 polyalkylene glycol Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 1
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 230000002335 preservative effect Effects 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 238000010583 slow cooling Methods 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 235000002639 sodium chloride Nutrition 0.000 description 1
- 239000001509 sodium citrate Substances 0.000 description 1
- NLJMYIDDQXHKNR-UHFFFAOYSA-K sodium citrate Chemical compound O.O.[Na+].[Na+].[Na+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O NLJMYIDDQXHKNR-UHFFFAOYSA-K 0.000 description 1
- 235000011083 sodium citrates Nutrition 0.000 description 1
- ZNCPFRVNHGOPAG-UHFFFAOYSA-L sodium oxalate Chemical compound [Na+].[Na+].[O-]C(=O)C([O-])=O ZNCPFRVNHGOPAG-UHFFFAOYSA-L 0.000 description 1
- 229940039790 sodium oxalate Drugs 0.000 description 1
- 229940074404 sodium succinate Drugs 0.000 description 1
- ZDQYSKICYIVCPN-UHFFFAOYSA-L sodium succinate (anhydrous) Chemical compound [Na+].[Na+].[O-]C(=O)CCC([O-])=O ZDQYSKICYIVCPN-UHFFFAOYSA-L 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000007711 solidification Methods 0.000 description 1
- 230000008023 solidification Effects 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- SFVFIFLLYFPGHH-UHFFFAOYSA-M stearalkonium chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCCCC[N+](C)(C)CC1=CC=CC=C1 SFVFIFLLYFPGHH-UHFFFAOYSA-M 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 150000005691 triesters Chemical class 0.000 description 1
- HNJXPTMEWIVQQM-UHFFFAOYSA-M triethyl(hexadecyl)azanium;bromide Chemical compound [Br-].CCCCCCCCCCCCCCCC[N+](CC)(CC)CC HNJXPTMEWIVQQM-UHFFFAOYSA-M 0.000 description 1
- PDSVZUAJOIQXRK-UHFFFAOYSA-N trimethyl(octadecyl)azanium Chemical compound CCCCCCCCCCCCCCCCCC[N+](C)(C)C PDSVZUAJOIQXRK-UHFFFAOYSA-N 0.000 description 1
- 239000006097 ultraviolet radiation absorber Substances 0.000 description 1
Landscapes
- Detergent Compositions (AREA)
- Cosmetics (AREA)
Description
本発明はパール剤分散液、更に詳細には、カチ
オン性界面活性剤、グリセリンモノ脂肪酸エステ
ル及びα−モノ(メチル分岐アルキル)グリセリ
ルエーテルによつてパール状結晶を生成させた、
結晶形が均一で、高温及び低温安定性に優れたパ
ール剤分散液に関する。
従来から、シヤンプー、リンス、化粧水等の外
観を美麗にしてその付加価値を高める目的で、外
観をパール状にすることが行われている。
斯かるパール剤分散液を調製する方法として
は、従来、例えば、雲母、魚鱗、オキシ塩化ビス
マス等の天然物あるいは無機物の粉砕物を配合す
る方法、または高級脂肪酸もしくはその塩、エチ
レングリコール高級脂肪酸エステル等の結晶を晶
出させる方法が採られていた。これらのうち、近
年一般に行われている方法は、エチレングリコー
ル高級脂肪酸エステルを用いる方法であり、これ
は常温固体の該エステルをシヤンプー等の製造時
に添加して加熱溶融し、次いでこれを冷却して該
エステルの結晶を生成させてパール状の外観を付
与させる方法である。そして、パール状の結晶を
晶出させる所謂パール剤としては、例えばエチレ
ングリコールジ高級脂肪酸エステル(特開昭57−
51799号、同57−156409号、同57−156410号、同
57−165308号)、ポリエチレンジカルボン酸エス
テル(特開昭57−67510号)、エチレングリコール
又はトリエチレングリコール脂肪酸ジエステル
(特開昭56−133400号)、及びポリアルキレングリ
コールジ脂肪酸エステル(特開昭57−48335号)
等が報告されている。
このような状況において、本発明者は、従来の
パール剤より安価で、粒径が均一で、外観美麗な
パール剤を活性剤中に安定に生成させることので
きるパール剤について鋭意研究を行つた結果、カ
チオン性界面活性剤、グリセリンモノ脂肪酸エス
テル及びα−モノ(メチル分岐アルキル)グリセ
リルエーテルを特定の比率で混合したものが上記
目的を達成することを見出し、本発明を完成し
た。
すなわち、本発明は、必須成分として、(A)カチ
オン性界面活性剤、(B)グリセリンモノ脂肪酸エス
テル及び(C)α−モノ(メチル分岐アルキル)グリ
セリルエーテルを含有し、これら3成分の総量が
1〜50重量%で、かつ(A)、(B)及び(C)の混合比が、
3成分系の三角図表において次の3点、
a 〔(A)=40.0、(B)=59.5、(C)=0.5〕
b 〔(A)=0.5、(B)=59.5、(C)=40.0〕
e 〔(A)=0.5、(B)=99.0、(C)=0.5〕
を結ぶ直線で囲まれた範囲内にあることを特徴と
するパール剤分剤液を提供するものである。
本発明の(A)成分であるカチオン界面活性剤とし
ては、特に制限はなく、ヘアーリンス剤に配合さ
れ得るすべてのものが利用されるが、次の式
()、
(式中、R1、R2、R3及びR4の1〜2個は炭素
数8〜20の長鎖アルキル基又は長鎖ヒドロキシア
ルキル基を示し、残余は炭素数1〜3のアルキル
基、ヒドロキシアルキル基、ベンジル基又は合計
付加モル数10以下のポリオキシエチレン基を示
し、Xはハロゲン原子又は炭素数1〜2のアルキ
ル硫酸基を示す)
で表わされる第4級アンモニウム塩が好ましく、
特に、ジステアリルジメチルアンモニウムクロラ
イド、ステアリルトリメチルアンモニウムメトサ
ルフエート、ステアリルトリメチルアンモニウム
クロライド、ステアリルジメチルベンジルアンモ
ニウムクロライド、ラウリルジエチルベンジルア
ンモニウムクロライド、ラウリルトリメチルアン
モニウムブロミド、ジステアリルメチルヒドロキ
シメチルクロライド、セチルトリメチルアンモニ
ウムクロライド、N−ステアリル−N,N,N−
トリ(ポリオキシエチレン)アンモニウムクロラ
イド(合計3モル付加)、セチルトリエチルアン
モニウムブロマイド、ステアリルジメチルアンモ
ニウムクロライド等が好ましい。
これらの(A)成分は、一種又は二種以上を混合し
てパール剤分散液中に0.05〜20重量%(以下単に
%で示す)、好ましくは0.5〜10%配合される。こ
の(A)成分の配合量が0.05%未満であると相分離を
起し、また20%を超えるとパール状光沢が失なわ
れるので好ましくない。
(B)成分のグリセリンモノ脂肪酸エステルは次の
一般式()、
(式中、R5は炭素数11〜23の直鎖又は分岐鎖
の飽和又は不飽和の炭化水素基を示す)で表わさ
れるグリセリンモノ脂肪酸エステルを主成分とす
るものが好ましい。この好ましい具体例として
は、例えばオレイン酸モノグリセライド、パルミ
チン酸モノグリセライド、イソステアリン酸モノ
グリセライド、ステアリン酸モノグリセライド、
ベヘニン酸モノグリセライド等を主成分とするも
のが挙げられる。一般にモノグリセライドと称し
て市販されているものは、モノエステルの外にジ
エステル、トリエステル、未反応グリセリン及び
脂肪酸に多量に含有しており、本発明の目的のた
めには適当でなく、本発明で優れたパール状光沢
を与えるには、80重量%以上の上記グリセリンモ
ノ脂肪酸エステルを含有していることが必要であ
る。
これらの(B)成分は、その融点以上の温度で分散
媒中に可溶化され均一液状になる必要があり、か
つパール状光沢の優れた結晶を析出させるために
は、パール剤分散液中に0.595〜49.5%、好まし
くは2〜20%配合される。
また、(C)成分のα−モノ(メチル分岐アルキ
ル)グリセリルエーテルは次の一般式()、
R6−OCH2CH(OH)CH2OH ()
(式中、R6は炭素数6〜24のメチル分岐の飽
和炭化水素基を示す)
で表わされるものが好ましい。これは、例えば特
開昭56−39033号に記載の方法によつて製造され
る。この好ましいものとしては、()式中のR6
が次の基()、
(式中、mは2いし14の整数、mは3ないし11
の整数であり、mとnの和は9ないし21である)
で表わされるものが挙げられ、このうち更に好ま
しいものは、式()中のmとnの和が11ないし
17(即ちアルキル基の合計炭素数が14ないし20)
のものであり、就中特にmとnの和が15(即ちア
ルキル基の合計炭素数が18)のものである。また
分岐メチル基はアルキル主鎖の中心近くのものが
好ましい。
次に、α−モノ(メチル分岐アルキル)グリセ
リルエーテルの代表的化合物の物性を示す。
The present invention uses a pearl agent dispersion, more specifically, a cationic surfactant, a glycerin monofatty acid ester, and an α-mono(methyl branched alkyl) glyceryl ether to produce pearl-like crystals.
This invention relates to a pearling agent dispersion having a uniform crystal shape and excellent high and low temperature stability. BACKGROUND ART Conventionally, shampoos, conditioners, lotions, etc. have been made to have a pearl-like appearance in order to beautify their appearance and increase their added value. Conventional methods for preparing such a pearl agent dispersion include, for example, a method of blending crushed natural or inorganic materials such as mica, fish scales, bismuth oxychloride, or higher fatty acids or their salts, ethylene glycol higher fatty acid esters, etc. A method was used to crystallize such crystals. Among these, the method that has been commonly used in recent years is the method of using ethylene glycol higher fatty acid ester, which is a method in which the ester, which is solid at room temperature, is added during the production of shampoo, etc., heated and melted, and then cooled. This is a method of forming crystals of the ester to give it a pearl-like appearance. As a so-called pearling agent that crystallizes pearl-like crystals, for example, ethylene glycol dihigher fatty acid ester (Japanese Patent Application Laid-Open No. 57-1989)
No. 51799, No. 57-156409, No. 57-156410, No. 57-156409, No. 57-156410, No.
57-165308), polyethylene dicarboxylic acid esters (JP 57-67510), ethylene glycol or triethylene glycol fatty acid diesters (JP 56-133400), and polyalkylene glycol difatty acid esters (JP 57-133400). −48335)
etc. have been reported. Under these circumstances, the present inventor conducted intensive research on a pearl agent that is cheaper than conventional pearl agents, has a uniform particle size, and can stably produce a pearl agent with a beautiful appearance in an activator. As a result, it was discovered that a mixture of a cationic surfactant, glycerin monofatty acid ester, and α-mono(methyl branched alkyl) glyceryl ether in a specific ratio achieved the above object, and the present invention was completed. That is, the present invention contains (A) a cationic surfactant, (B) glycerin monofatty acid ester, and (C) α-mono(methyl branched alkyl) glyceryl ether as essential components, and the total amount of these three components is 1 to 50% by weight, and the mixing ratio of (A), (B) and (C) is
In the triangular diagram of the three-component system, the following three points are a [(A)=40.0, (B)=59.5, (C)=0.5] b [(A)=0.5, (B)=59.5, (C)= 40.0] e [(A) = 0.5, (B) = 99.0, (C) = 0.5] The present invention provides a pearlescent agent dispensing liquid characterized by being within a range surrounded by a straight line connecting (A)=0.5, (B)=99.0, (C)=0.5]. The cationic surfactant that is the component (A) of the present invention is not particularly limited, and any surfactant that can be incorporated into a hair rinse agent may be used, but the following formula (), (In the formula, 1 to 2 of R 1 , R 2 , R 3 and R 4 represent a long chain alkyl group or a long chain hydroxyalkyl group having 8 to 20 carbon atoms, and the rest are alkyl groups having 1 to 3 carbon atoms. , represents a hydroxyalkyl group, a benzyl group, or a polyoxyethylene group having a total number of added moles of 10 or less, and X represents a halogen atom or an alkyl sulfate group having 1 to 2 carbon atoms).
In particular, distearyldimethylammonium chloride, stearyltrimethylammonium methosulfate, stearyltrimethylammonium chloride, stearyldimethylbenzylammonium chloride, lauryldiethylbenzylammonium chloride, lauryltrimethylammonium bromide, distearylmethylhydroxymethyl chloride, cetyltrimethylammonium chloride, N -stearyl-N,N,N-
Preferred are tri(polyoxyethylene)ammonium chloride (3 moles added in total), cetyltriethylammonium bromide, stearyldimethylammonium chloride, and the like. One or more of these components (A) are blended in the pearlescent agent dispersion in an amount of 0.05 to 20% by weight (hereinafter simply expressed as %), preferably 0.5 to 10%. If the amount of component (A) is less than 0.05%, phase separation will occur, and if it exceeds 20%, the pearly luster will be lost, which is not preferable. The glycerin monofatty acid ester of component (B) has the following general formula (), (In the formula, R 5 represents a straight chain or branched chain saturated or unsaturated hydrocarbon group having 11 to 23 carbon atoms.) It is preferable to use a glycerin monofatty acid ester as a main component. Preferred specific examples include oleic acid monoglyceride, palmitic acid monoglyceride, isostearic acid monoglyceride, stearic acid monoglyceride,
Examples include those whose main component is behenic acid monoglyceride. Generally, commercially available monoglycerides contain large amounts of diesters, triesters, unreacted glycerin, and fatty acids in addition to monoesters, and are not suitable for the purpose of the present invention. In order to provide excellent pearly luster, it is necessary to contain 80% by weight or more of the above-mentioned glycerin monofatty acid ester. These (B) components need to be solubilized in the dispersion medium at a temperature higher than their melting point and become a uniform liquid, and in order to precipitate crystals with excellent pearl-like luster, they must be added to the pearling agent dispersion. It is blended in an amount of 0.595 to 49.5%, preferably 2 to 20%. In addition, the α-mono(methyl branched alkyl)glyceryl ether of component (C) has the following general formula (), R 6 −OCH 2 CH(OH)CH 2 OH () (wherein, R 6 has 6 to 6 carbon atoms). 24 (representing a methyl-branched saturated hydrocarbon group) is preferred. This is produced, for example, by the method described in JP-A-56-39033. As a preferable example, R 6 in the formula ()
is the next group (), (In the formula, m is an integer from 2 to 14, m is 3 to 11
, and the sum of m and n is 9 to 21). Among these, more preferable ones are those in which the sum of m and n in formula ( ) is 11 to 21
17 (i.e. the total number of carbon atoms in the alkyl group is 14 to 20)
Among them, the sum of m and n is 15 (ie, the total number of carbon atoms in the alkyl group is 18). Further, the branched methyl group is preferably one near the center of the alkyl main chain. Next, the physical properties of representative compounds of α-mono(methyl branched alkyl)glyceryl ether are shown.
【表】
これらの(C)成分は、パール剤分散液中に0.05〜
40%、好ましくは0.1〜20%配合される。
本発明のパール剤分散液は、上記(A)、(B)及び(C)
成分を必須成分として含有するが、更にこれら3
成分は総量が1〜50%、好ましくは5〜30%で、
(A)、(B)及び(C)の混合比が、3成分系の三角図表
(第1図)において、前記3点(a,b,c)を
結ぶ直線で囲まれた範囲内にあることが必要であ
る。
本発明のパール剤分散液は、(A)、(B)及び(C)を含
む溶液を加熱して均一溶液となし、次いでこれを
強制冷却又は自然冷却して結晶を晶析させること
により製造される。
本発明において、パール化を促進させるため
に、公知の成核剤及びハイドロトロープ剤を配合
することができる。成核剤としては、塩化ナトリ
ウム、塩化アンモニウム、硫酸ナトリウム、クエ
ン酸ナトリウム、コハク酸ナトリウム、シユウ酸
ナトリウム等の水溶性無機塩またはクエン酸、コ
ハク酸、シユウ酸、尿素等が挙げられ、これらは
1種又は2種以上を0.1〜5%添加配合される。
また、ハイドロトロープ剤としては、エチルアル
コール、イソプロピルアルコール、グリセリン、
プロピレングリコール、1,3−ブチレングリコ
ール、ソルビトール、ポリエチレングリコール等
が挙げられ、これらは1種又は2種以上を1〜50
%添加配合される。更にまた、生成したパール状
結晶を安定に保持するために、セルロース誘導
体、ポリビニルピロリドン、メトキシエチレン無
水マレイン酸共重合体等の水溶性高分子化合物を
配合することができる。特に好ましい水溶性高分
子化合物は、次の一般式で表わされるものであ
る。
〔R7は水素原子、基(−CH2CH2O)−nH(mは1
〜5の整数)、基−CH2、基−C2H5、基−
C3H6OHの1種又は2種以上を示し、mは5〜
5000の数を示す〕
これらの水溶性高分子化合物は、1種又は2種
以上を0.1〜5重量%添加配合される。
本発明のパール剤分散液の前記製造法におい
て、その撹拌速度は特に限定されず、10〜
100rpmの程度の低速回転で充分である。この際
上記成核剤及び安定化剤は予め分散媒中に溶かし
ておくのが好ましい。また、パール化を速かに起
させるためには、液温を0〜20℃に下げて行うの
が好ましい。冷却方法は特に制限なく、徐冷、急
冷の何れの方法でもよい。
このようにすれば、冷却に従つて液全体が美麗
なパール状光沢を有するようになる。この組成物
には、更に必要に応じて、PH調整剤、防腐剤、色
素、香料、紫外線吸収剤等を添加することができ
る。PHは4〜11、特に7〜10の範囲に調整するの
が好ましい。
斯くして得られた本発明のパール剤分散液は、
液体洗浄組成物、液体リンス等の液状組成物及び
ペースト状組成物に、その用途に応じて必要量が
配合され、これら組成物に美麗なパール状光沢を
与えることができる。この場合の上記組成物に対
するパール剤分散液の添加量は、例えば、液体組
成物においては、1〜20%、好ましくは2〜10%
である。
叙上の如くして得られたパール剤分散液は、そ
の中の結晶の粒径が約1〜10μと微細なものであ
るため、約30μ以上の粒径の粒子よりなる従来の
溶融パール剤分散液と比べ、均一で美しい外観を
有するものである。
次に実施例を挙げ本発明を説明するが、本発明
は、これら実施例に限定されるものでない。な
お、本実施例中で用いた試験方法は次の通りであ
る。
(1) 外 観
100ml容の透明ガラス容器に試料を入れ、肉
眼にてパール光沢の外観を観察した。尚、試料
に気泡の混入しているものは遠心分離器に掛
け、脱泡を行なつた。
〇=パール光沢が均一である。
×=濁り、エマルシヨン様又は、パール光沢が
不均一なもの。
(2) 高温安定性
透明ガラス容器に試料を入れ、密閉し、50℃
の恒温槽中に一か月保存した後、試料の分離の
有無、パール光沢剤の凝集の有無を肉眼観察し
た。
〇=分離、パール光沢剤の凝集、パール光沢の
消失等異常を認めない。
×=分離、パール光沢剤の凝集、パール光沢の
消失のいずれかの異常を認める。
(3) 低温安定性
透明ガラス容器に試料を入れ、密閉し、−15
℃の恒温槽中に一か月保存した後、試料の分
離、固結の有無を肉眼観察した。
〇=分離、固結等なく流動性のあるもの。
×=分離、固結等異常のあるもの。
実施例 1
ジステアリルジメチルアンモニウムクロライ
ド 1(%)
ベヘニン酸モノグリセライド(モノエステル
含有量90%) 8
α−モノ(イソステアリル)グリセリルエー
テル〔()式中、m=7、n=8のもの〕
1
水 90
80℃に加熱したに、同温に加熱して溶解した
、、の混合物を加え、撹拌しながら、20℃
まで冷却する。本組成物はパール状外観を呈し、
保存安定性も良好であつた。
実施例 2
モノベヘニルトリメチルアンモニウムクロラ
イド 0.4(%)
モノセチルトリメチルアンモニウムクロライ
ド 0.6
ステアリン酸モノグリセライド(モノエステ
ル含有量90%) 8.5
α−モノ(イソステアリル)グリセリルエー
テル〔()式中、m=7、n=8のもの〕
0.5
水 90
80℃に加熱したに、同温度に加熱して溶解し
た〜を加え、撹拌しながら20℃まで冷却す
る。本組成物はパール状外観を呈し、保存安定性
も良好であつた。
実施例 3
第1表に示す通りの各成分を種々の割合で配合
し、実施例1に示す方法で、パール剤分散液を調
製した。得られた分散液を評価した結果を第1表
に示す。[Table] These (C) components are contained in the pearl agent dispersion at a concentration of 0.05~
40%, preferably 0.1 to 20%. The pearl agent dispersion of the present invention includes the above (A), (B) and (C).
Contains these three ingredients as essential ingredients, but in addition, these three
The total amount of ingredients is 1 to 50%, preferably 5 to 30%,
The mixing ratio of (A), (B) and (C) is within the range surrounded by the straight line connecting the three points (a, b, c) in the triangular diagram of the ternary component system (Figure 1). It is necessary. The pearl agent dispersion of the present invention is produced by heating a solution containing (A), (B), and (C) to form a homogeneous solution, and then forcing or naturally cooling the solution to crystallize the crystals. be done. In the present invention, known nucleating agents and hydrotropic agents can be blended to promote pearlization. Nucleating agents include water-soluble inorganic salts such as sodium chloride, ammonium chloride, sodium sulfate, sodium citrate, sodium succinate, sodium oxalate, citric acid, succinic acid, oxalic acid, urea, etc. One or more types are added in an amount of 0.1 to 5%.
In addition, hydrotropic agents include ethyl alcohol, isopropyl alcohol, glycerin,
Examples include propylene glycol, 1,3-butylene glycol, sorbitol, polyethylene glycol, etc., and these include one or more of them at 1 to 50%
% added. Furthermore, in order to stably maintain the produced pearl-like crystals, a water-soluble polymer compound such as a cellulose derivative, polyvinylpyrrolidone, or methoxyethylene-maleic anhydride copolymer may be blended. Particularly preferred water-soluble polymer compounds are those represented by the following general formula. [R 7 is a hydrogen atom, group (-CH 2 CH 2 O) - n H (m is 1
-5 integer), group -CH 2 , group -C 2 H 5 , group -
Indicates one or more types of C 3 H 6 OH, m is 5 to
5000] One or more of these water-soluble polymer compounds are added in an amount of 0.1 to 5% by weight. In the method for producing the pearl agent dispersion of the present invention, the stirring speed is not particularly limited, and is
A low rotation speed of about 100 rpm is sufficient. At this time, it is preferable that the above-mentioned nucleating agent and stabilizer be dissolved in the dispersion medium in advance. In addition, in order to quickly cause pearlization, it is preferable to lower the liquid temperature to 0 to 20°C. The cooling method is not particularly limited and may be either slow cooling or rapid cooling. In this way, the entire liquid will have a beautiful pearl-like luster as it cools. If necessary, a PH regulator, preservative, pigment, fragrance, ultraviolet absorber, etc. can be added to this composition. It is preferable to adjust the pH to a range of 4 to 11, particularly 7 to 10. The thus obtained pearl agent dispersion of the present invention is
A necessary amount is blended into liquid compositions such as liquid cleaning compositions, liquid rinses, and paste compositions depending on the intended use, and it is possible to impart beautiful pearl-like luster to these compositions. In this case, the amount of the pearl agent dispersion added to the above composition is, for example, 1 to 20%, preferably 2 to 10% in the liquid composition.
It is. The pearling agent dispersion obtained as described above has a fine crystal grain size of about 1 to 10 μm, so it is different from the conventional molten pearl agent having particles with a particle size of about 30 μm or more. It has a more uniform and beautiful appearance than a dispersion. Next, the present invention will be explained with reference to Examples, but the present invention is not limited to these Examples. The test method used in this example is as follows. (1) Appearance A sample was placed in a 100ml transparent glass container, and the appearance of pearlescent luster was observed with the naked eye. If the sample contained air bubbles, it was centrifuged to remove air bubbles. 〇 = Pearl luster is uniform. × = cloudy, emulsion-like, or non-uniform pearl luster. (2) High temperature stability Place the sample in a transparent glass container, seal it, and store at 50℃.
After being stored in a constant temperature bath for one month, the presence or absence of separation of the sample and the presence or absence of aggregation of the pearlescent agent were visually observed. 〇=No abnormalities such as separation, aggregation of pearlescent agent, loss of pearlescent luster, etc. are observed. ×= Any abnormality such as separation, aggregation of pearlescent agent, or loss of pearlescent luster is observed. (3) Low-temperature stability Place the sample in a transparent glass container, seal it, and keep it at -15
After being stored in a constant temperature bath at ℃ for one month, the samples were visually observed for separation and solidification. 〇 = Fluid without separation or caking. × = Abnormalities such as separation and caking. Example 1 Distearyldimethylammonium chloride 1 (%) Behenic acid monoglyceride (monoester content 90%) 8 α-Mono(isostearyl)glyceryl ether [In the formula (), m = 7, n = 8]
1 Add the mixture of water heated to 90 80℃, heated to the same temperature and dissolved, and stir to 20℃.
Cool until cool. The composition exhibits a pearl-like appearance;
The storage stability was also good. Example 2 Monobehenyltrimethylammonium chloride 0.4 (%) Monocetyltrimethylammonium chloride 0.6 Stearic acid monoglyceride (monoester content 90%) 8.5 α-mono(isostearyl)glyceryl ether [(in the formula, m = 7, n =8 things]
0.5 Water 90 Add ~ heated to 80°C and dissolved at the same temperature, and cool to 20°C while stirring. This composition exhibited a pearl-like appearance and had good storage stability. Example 3 A pearling agent dispersion was prepared by blending the components shown in Table 1 in various proportions and using the method shown in Example 1. Table 1 shows the results of evaluating the obtained dispersion.
【表】
この結果から明らかな如く、十分満足のゆくパ
ール剤分散液が得られるのは、三成分(A)、(B)、(C)
の混合比が第1図a,b,cの3点を結ぶ直線で
囲まれた範囲内のものだけである。
実施例 4
第2表に示す組成のパール剤分散液を調製し、
得られた分散液の評価をおこなつた。組成物の調
製方法及び評価方法は実施例1と同一である。[Table] As is clear from the results, the three components (A), (B), and (C) can provide a fully satisfactory pearling agent dispersion.
The mixture ratio is only within the range surrounded by the straight line connecting the three points a, b, and c in Figure 1. Example 4 A pearling agent dispersion having the composition shown in Table 2 was prepared,
The obtained dispersion liquid was evaluated. The preparation method and evaluation method of the composition are the same as in Example 1.
【表】【table】
第1図は、本発明パール剤分散液の(A)、(B)及び
(C)成分の配合比率を示す三角図である。
A…カチオン界面活性剤、B…グリセリンモノ
脂肪酸エステル、C…α−モノ(メチル分岐アル
キル)グリセリルエーテル。
Figure 1 shows (A), (B) and
(C) It is a triangular diagram showing the blending ratio of the component. A...Cationic surfactant, B...Glycerin monofatty acid ester, C...α-mono(methyl branched alkyl) glyceryl ether.
Claims (1)
(B)グリセリンモノ脂肪酸エステル及び(C)α−モノ
(メチル分岐アルキル)グリセリルエーテルを含
有し、これら3成分の総量が1〜50重量%で、か
つ(A)、(B)及び(C)の混合比が、3成分系の三角図表
において次の3点、 a 〔(A)=40.0、(B)=59.5、(C)=0.5〕 b 〔(A)=0.5、(B)=59.5、(C)=40.0〕 e 〔(A)=0.5、(B)=99.0、(C)=0.5〕 を結ぶ直線で囲まれた範囲内にあることを特徴と
するパール剤分剤液。 2 カチオン性界面活性剤が次の一般式()、 (式中、R1,R2,R3及びR4の1〜2個は炭素
数8〜20の長鎖アルキル基又は長鎖ヒドロキシア
ルキル基を示し、残余は炭素数1〜3のアルキル
基、ヒドロキシアルキル基、ベンジル基又は合計
付加モル数10以下のポリオキシエチレン基を示
し、Xはハロゲン原子又は炭素数1〜2のアルキ
ル硫酸基を示す) で表わされるものである特許請求の範囲第1項記
載のパール剤分散液。 3 グリセリンモノ脂肪酸エステルが、次の一般
式()、 (式中、R5は炭素数11〜23の直鎖又は分岐鎖
の飽和又は不飽和の炭化水素基を示す)で表わさ
れるグリセリンモノ脂肪酸エステルを主成分とす
るものである特許請求の範囲第1項記載のパール
剤分散液。 4 グリセリンモノ脂肪酸エステルが、一般式
()で表わされるものを80重量%以上含有する
ものである特許請求の範囲第3項記載のパール剤
分散液。 5 α−モノ(メチル分岐アルキル)グリセリル
エーテルが、次の一般式()、 R6−OCH2CH(OH)CH2OH () (式中、R6は炭素数6〜24のメチル分岐の飽
和炭化水素基を示す) で表わされるものである特許請求の範囲第1項記
載のパール剤分散液。 6 α−モノ(メチル分岐アルキル)グリセリル
エーテルが、()式中のR6が次の基()、 (式中、mは2ないし14の整数、aは3ないし
11の整数であり、mとnの和は9ないし21であ
る) で表わされるものである特許請求の範囲第5項記
載のパール剤分散液。[Claims] 1. As an essential component, (A) a cationic surfactant;
(B) contains glycerin monofatty acid ester and (C) α-mono(methyl branched alkyl) glyceryl ether, the total amount of these three components is 1 to 50% by weight, and (A), (B) and (C) The mixing ratio of is the following three points in the triangular diagram of the three-component system: a [(A)=40.0, (B)=59.5, (C)=0.5] b [(A)=0.5, (B)=59.5 , (C) = 40.0] e [(A) = 0.5, (B) = 99.0, (C) = 0.5]. 2 The cationic surfactant has the following general formula (), (In the formula, 1 to 2 of R 1 , R 2 , R 3 and R 4 represent a long-chain alkyl group or a long-chain hydroxyalkyl group with 8 to 20 carbon atoms, and the rest are alkyl groups with 1 to 3 carbon atoms. , a hydroxyalkyl group, a benzyl group, or a polyoxyethylene group having a total number of added moles of 10 or less, and X represents a halogen atom or an alkyl sulfate group having 1 to 2 carbon atoms. Pearl agent dispersion according to item 1. 3 Glycerin monofatty acid ester has the following general formula (), (In the formula, R 5 represents a straight chain or branched chain saturated or unsaturated hydrocarbon group having 11 to 23 carbon atoms.) Pearl agent dispersion according to item 1. 4. The pearl agent dispersion according to claim 3, wherein the glycerin monofatty acid ester contains 80% by weight or more of one represented by the general formula (). 5 α-Mono(methyl-branched alkyl)glyceryl ether has the following general formula (), R 6 -OCH 2 CH(OH)CH 2 OH () (wherein R 6 is a methyl-branched The pearlescent agent dispersion according to claim 1, which is represented by the formula (representing a saturated hydrocarbon group). 6 α-mono(methyl branched alkyl) glyceryl ether is represented by the following formula (), where R 6 is the following group (), (In the formula, m is an integer from 2 to 14, a is from 3 to
11, and the sum of m and n is from 9 to 21.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP11670383A JPS608215A (en) | 1983-06-28 | 1983-06-28 | Dispersion of pearl agent |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP11670383A JPS608215A (en) | 1983-06-28 | 1983-06-28 | Dispersion of pearl agent |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS608215A JPS608215A (en) | 1985-01-17 |
| JPH0443043B2 true JPH0443043B2 (en) | 1992-07-15 |
Family
ID=14693738
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP11670383A Granted JPS608215A (en) | 1983-06-28 | 1983-06-28 | Dispersion of pearl agent |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS608215A (en) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3837860A1 (en) * | 1988-11-08 | 1990-05-10 | Wella Ag | STORAGE HAIR CONDITIONER WITH PEARL GLOSS |
| JP3340126B2 (en) * | 1990-03-02 | 2002-11-05 | 株式会社資生堂 | Oil-in-water emulsion composition containing non-steroidal anti-inflammatory drug |
-
1983
- 1983-06-28 JP JP11670383A patent/JPS608215A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS608215A (en) | 1985-01-17 |
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