CN103145995A - 硅酮改性蜡、含有该硅酮改性蜡的组合物、化妆品、及硅酮改性蜡的制造方法 - Google Patents
硅酮改性蜡、含有该硅酮改性蜡的组合物、化妆品、及硅酮改性蜡的制造方法 Download PDFInfo
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- CN103145995A CN103145995A CN2012105201559A CN201210520155A CN103145995A CN 103145995 A CN103145995 A CN 103145995A CN 2012105201559 A CN2012105201559 A CN 2012105201559A CN 201210520155 A CN201210520155 A CN 201210520155A CN 103145995 A CN103145995 A CN 103145995A
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Abstract
本发明是一种硅酮改性蜡,其特征在于,其是通过使在1分子中具有1个或2个烯基的多元醇与高级脂肪酸发生酯化反应,并使所得生成物与含有至少1个甲基的有机氢聚硅氧烷发生氢化硅烷化反应而获得,且在25℃下为固体或具有触变性的油脂状。由此,提供一种硅酮改性蜡及其制造方法、包含该硅酮改性蜡的组合物、及化妆品,其中,所述硅酮改性蜡对挥发性及不挥发性硅酮油、烃油、酯油、及天然动植物油剂的相溶性较高,并可以使各种油剂呈膏状或固化,且在25℃下为固体或具有触变性的油脂状。
Description
技术领域
本发明涉及一种硅酮改性蜡、含有该硅酮改性蜡的组合物、化妆品、及硅酮改性蜡的制造方法。
背景技术
蜡等油性增粘剂或胶化剂(以下统一称为“增粘剂”),是用于提高化妆品中的油性成分的粘度,并改善化妆品的可用性、稳定性、及外观等。作为该油性增粘剂,广泛利用:纯白地蜡(ceresin)、聚乙烯、及地蜡(ozokerite)等烃系蜡;或巴西棕榈蜡(carnauba wax)、小烛树蜡(candelilla wax)等蜡;或蔗糖棕榈酸酯等多糖脂肪酸酯等。
这些增粘剂在调配至化妆品中时,一般需要在增粘剂的熔点以上的温度下熔化。因此,当调配熔点较高的增粘剂时,有时会导致化妆品中的其他成分劣化或分解。因此,期望为熔点较低的增粘剂,尤其是熔点在100℃以下的增粘剂。然而,熔点较低的增粘剂,通常增粘效果较低,在夏季等情况下,有时会引起化妆品的粘度降低或相位分离。
并且,期望增粘剂与调配至化妆品中的低粘度的油剂的相溶性良好。如果相溶性较差,有时会历时而与油剂分离;或在冷却时,增粘剂的结晶变大,从而损害化妆品的外观或触感。硅酮油由于具有触感干爽、涂匀性良好、及防水性良好等优异特性,因此,常用于化妆品用油剂。其中,挥发性硅酮油由于构成无粘性且触感轻盈的化妆品,而经常被使用。然而,硅酮油与一般油剂的相溶性、及与增粘剂的适合性较差,容易引起上述问题。
为了解决上述问题,开发出一种可以使挥发性硅酮油增粘的增粘剂(专利文献1、专利文献2)。然而,这些难以单独使硅酮油顺利地增粘,并且所获得的增粘物缺少化妆品所要求的光滑性。因此,作为解决这些问题的对策,提出一种硅改性烯烃系蜡(专利文献3)。
在将上述增粘剂调配至化妆品中时,与油剂一起加热溶解。加热溶解的 温度并不明确,但一般在蜡的熔点以上。在将上述硅改性烯烃系蜡与油剂一起加热溶解之后,冷却并恢复为室温,此时,可以获得一种无流动性的硅系室温固化组合物,可以使用该组合物作为化妆品(专利文献3,第0195段)。然而,该组合物在涂匀性、触感方面,存在改良的余地。
现有技术文献
专利文献
专利文献1:日本专利第4664991号
专利文献2:WO2004/110393
专利文献3:日本特开2008-174571号公报
发明内容
本发明是鉴于上述情况而完成,目的在于提供一种硅酮改性蜡及其制造方法、含有该硅酮改性蜡的组合物、及化妆品,其中,该硅酮改性蜡对挥发性及不挥发性硅酮油、烃油、酯油、及天然动植物油剂等油剂的相溶性较高,并可以将各种油剂增粘,使其成为光滑且涂匀性良好的膏状或固体状组合物。
为了解决上述课题,根据本发明,提供一种硅酮改性蜡,其特征在于,其是通过使在1分子中具有1个或2个烯基的多元醇与高级脂肪酸发生酯化反应,并使所得生成物与含有至少1个甲基的有机氢聚硅氧烷(organohydrogen polysiloxane)发生氢化硅烷化反应而获得,且在25℃下为固体或具有触变性的油脂状。
这种本发明的硅酮改性蜡,由于对挥发性及不挥发性硅酮油、烃油、酯油、及天然动植物油剂等油剂的相溶性较高,并可以使各种油剂呈膏状或固化,因此,尤其是作为调配至化妆品中的增粘剂,极为有用。并且,含有本发明的硅酮改性蜡的组合物,呈光滑且涂匀性良好的膏状或固体状组合物。
并且,优选为,前述在1分子中具有1个或2个烯基的多元醇,是具有直链或支链状聚甘油(polyglycerin)结构的化合物;
前述高级脂肪酸,是碳数12~30的直链状饱和型高级脂肪酸;并且,
前述有机氢聚硅氧烷,是由下述通式(A)所记载的有机氢聚硅氧烷,
(式中,R1、R2、R3、R4分别独立地表示氢原子、相同或不同且可以具有分支聚丙三醇链键结的连结基或取代基且碳数1~22的直链或支链的烷基或烷氧基、碳数6~22的芳基、及氟取代烷基中的任一个;其中,R1、R3中至少1个表示氢原子,R2、R4中至少1个表示甲基;n表示0~100的整数)。
如果是这种硅酮改性蜡,那么对挥发性及不挥发性硅酮油、烃油、酯油、及天然动植物油剂等油剂的相溶性更高,可以进一步确实地使各种油剂呈膏状或固化。
并且,前述硅酮改性蜡的熔点(常压)可以为40~100℃。
由于本发明的硅酮改性蜡的熔点为40~100℃,因此,在夏季等情况下,不会引起化妆品的粘度降低或相位分离,且不会导致化妆品中的其他成分劣化或分解,因而优选。
并且,在本发明中,提供一种组合物,特征在于:含有5~40质量%的前述硅酮改性蜡,且在25℃常压下为膏状或固体状。
由于本发明的硅酮改性蜡与硅酮油等油剂的相溶性较高,并且增粘效果较高,因此,可以使各种油剂成为光滑且涂匀性良好的、膏状或固体状的组合物(25℃常压),且可以适当地将该组合物调配至化妆品中。
并且,在本发明中,提供一种化妆品,其特征在于,其含有硅酮改性蜡。
本发明的硅酮改性蜡,由于对化妆品所使用的各种油剂的相溶性较高,且可以使各种油剂成为光滑且涂匀性良好的膏状或固体状的组合物,因此,适合用于化妆品。进一步,本发明的硅酮改性蜡,由于熔点可以达到40~100℃,进一步达到50~80℃,因此,在夏季等情况下,不会引起化妆品的粘度降低或相位分离,且不会导致化妆品中的其他成分劣化或分解。
并且,在本发明中,提供一种硅酮改性蜡的制造方法,其特征在于,其包括:工序(Ⅰ),在催化剂存在下,使在1分子中具有1个或2个烯基的多元醇与高级脂肪酸发生酯化反应,得到酯化反应生成物;及,工序(Ⅱ),在催化剂存在下,使前述酯化反应生成物与含有至少1个甲基的有机氢聚硅氧 烷发生氢化硅烷化反应。
根据本发明的硅酮改性蜡的制造方法,可以制造一种硅酮改性蜡,所述硅酮改性蜡对挥发性及不挥发性硅酮油、烃油、酯油、及天然动植物油剂等油剂的相溶性较高,并可以使各种油剂呈膏状或固化。
并且,优选为,作为前述在1分子中具有1个或2个烯基的多元醇,使用具有直链或支链状聚甘油结构的化合物;
作为前述高级脂肪酸,使用碳数12~30的直链状饱和型高级脂肪酸;并且,
作为前述有机氢聚硅氧烷,使用由下述通式(A)所记载的有机氢聚硅氧烷,
(式中,R1、R2、R3、R4分别独立地表示氢原子、相同或不同且可以具有分支聚丙三醇链键结的连结基或取代基且碳数1~22的直链或支链的烷基或烷氧基、碳数6~22的芳基、及氟取代烷基中的任一个;其中,R1、R3中至少1个表示氢原子,R2、R4中至少1个表示甲基;n表示0~100的整数)。
如果是这种硅酮改性蜡的制造方法,那么可以制造一种硅酮改性蜡,所述硅酮改性蜡对挥发性及不挥发性硅酮油、烃油、酯油、及天然动植物油剂等油剂的相溶性更高,可以进一步确实地使各种油剂呈膏状或固化。
本发明的硅酮改性蜡,对挥发性及不挥发性硅酮油、烃油、酯油、及天然动植物油剂等油剂的相溶性较高,并可以使各种油剂成为光滑且涂匀性良好的膏状或固体状组合物。并且,由于熔点为40~100℃,因此,在夏季等情况下,可以防止化妆品的粘度降低或相位分离,成为组合物时(加热熔化时),可以防止其他成分劣化或分解,因而可以适合作为化妆品来使用。
具体实施方式
以下,更详细地说明本发明。
如上所述,需要一种增粘剂,所述增粘剂对挥发性及不挥发性硅酮油、 烃油、酯油、及天然动植物油剂等油剂的相溶性较高,并可以使各种油剂呈膏状或固化。
本发明人为解决上述课题而锐意研究,结果发现一种硅酮改性蜡,它对挥发性及不挥发性硅酮油、烃油、酯油、及天然动植物油剂等油剂的相溶性较高,并可以将各种油剂增粘,使其成为光滑且涂匀性良好的膏状或固体状组合物,其中,所述硅酮改性蜡的特征在于:其是通过使在1分子中具有1个或2个烯基的多元醇与高级脂肪酸发生酯化反应,并使所得生成物与含有至少1个甲基的有机氢聚硅氧烷发生氢化硅烷化反应而获得,且在25℃下为固体或具有触变性的油脂状。
以下,进一步详细地说明本发明。
即,在本发明中,提供一种硅酮改性蜡,其特征在于,其是通过使在1分子中具有1个或2个烯基的多元醇与高级脂肪酸发生酯化反应,并使所得生成物与含有至少1个甲基的有机氢聚硅氧烷发生氢化硅烷化反应而获得,且在25℃下为固体或具有触变性的油脂状。
并且,在本发明中,提供一种硅酮改性蜡的制造方法,其特征在于,其包括:工序(Ⅰ),在催化剂存在下,使在1分子中具有1个或2个烯基的多元醇与高级脂肪酸发生酯化反应,得到酯化反应生成物;及,工序(Ⅱ),在催化剂存在下,使前述酯化反应生成物与含有至少1个甲基的有机氢聚硅氧烷发生氢化硅烷化反应。
作为本发明所使用的在1分子中具有1个或2个烯基的多元醇,可以列举具有下述结构式(B)、(C)、(D)、(E)中的任一个且为直链或支链状且含有1个或2个烯基的聚甘油。
并且,优选为,可以使用末端是烯基的聚甘油,例如,优选下述三甘油(triglycerin)衍生物、四甘油(tetraglycerin)衍生物,并可以使用下述聚甘油。
(上述式中,a、b、c、d分别为2或3。)
并且,作为本发明所使用的具有1个或2个烯基的多元醇的结构,也可以具有直链状、支链状,进一步可以具有环状醚结构。
作为这些含有烯基的多元醇的制造方法,可以通过在氢氧化钾等碱性催化剂存在下,使甘油、或双甘油、三甘油等聚甘油、与烯丙基缩水甘油醚(allylglycidyl ether)反应而获得。优选为,将反应温度控制在60~120℃。反应后,通过中和碱性催化剂,然后馏出低沸点成分,可以获得目标物(具有1个或2个烯基的多元醇)。
本发明所使用的高级脂肪酸,优选碳数12~30,进一步优选碳数18~26的直链饱和脂肪酸。作为该高级脂肪酸的一例,可以列举:肉豆蔻酸、棕榈酸、硬脂酸、油酸、花生酸、山嵛酸、木蜡酸、蜡酸、褐煤酸、及蜂花酸等;并使用其中的一种或两种以上。
然后,通过将上述在1分子中具有1个或2个烯基的多元醇与高级脂肪酸装入反应容器中,并在惰性气体气流中,160~240℃下,一边去除反应所生成的水,一边进行5~30小时左右的酯化反应,酯化反应结束后,利用常用方法进行脱色、除臭等精制处理,可以获得酯化反应生成物。
酯化反应时,可以根据需要而使用酸催化剂、金属催化剂、及回流溶剂。
与上述酯化反应生成物发生氢化硅烷化反应、且含有至少1个甲基的有机氢聚硅氧烷,是在1分子中具有直接键结于硅原子的氢原子、直接键结于硅原子的甲基各至少1个的有机聚硅氧烷,可以列举由下述结构式(A)所表示的有机氢聚硅氧烷。
(式中,R1、R2、R3、R4分别独立地表示氢原子、相同或不同且可以具有分支聚丙三醇链键结的连结基或取代基且碳数1~22的直链或支链的烷基或烷氧基、碳数6~22的芳基、及氟取代烷基中的任一个;其中,R1、R3中至少1个表示氢原子,R2、R4中至少1个表示甲基;n表示0~100的整数)。
作为R1,优选为氢原子、碳数1~6的烷基,尤其优选为氢原子、甲基、及丁基。R2优选为碳数1~6的烷基,尤其优选为甲基。R3优选为氢原子、碳数1~6的烷基,尤其优选为氢原子、甲基。R4优选为碳数~6的烷基,尤其优选为甲基。
在这些中,优选为具有1~5个键结于硅原子的氢原子(Si-H基)的有机氢聚硅氧烷,更优选具有1~2个,尤其优选为具有1个键结于硅原子的氢原子的有机氢聚硅氧烷。进一步优选为,在分子单侧末端具有Si-H基的α-氢有机聚硅氧烷(hydrogen organo polysiloxane)。
n为0~100的整数,优选为0~50,更优选为1~20,尤其优选1为~10的整数。
具体来说,例示下述式。
(式中,n如上所述。)
作为本发明所使用的有机氢聚硅氧烷的合成方法,通过将六甲基二硅氧烷、八甲基环四硅氧烷(D4)与四甲基四氢环四硅氧烷(H4)装入反应容器中,并加入酸催化剂,在常温下搅拌一晚后,进行中和、脱色、及除臭等精制处理,可以获得甲基氢硅氧烷。
使上述甲基氢有机聚硅氧烷与具有烯基的甘油衍生物(前述酯化反应生成物)加成,使Si-H基/烯基的摩尔比为0.5以上且不足1.5,优选为0.8以上且不足1.2。
优选为,该加成反应是在铂催化剂或铑催化剂的存在下进行。作为优选的催化剂的一例,可以列举:氯铂酸、醇改性氯铂酸、及氯铂酸-乙烯基硅氧烷络合物等。
上述加成反应也可以根据需要,在有机溶剂中进行。作为有机溶剂,可以列举例如:甲醇、乙醇、2-丙醇、及丁醇等脂肪族醇;甲苯、二甲苯等芳香族烃;正戊烷、正己烷、及环己烷等脂肪族或脂环族烃;及,二氯甲烷、三氯甲烷、及四氯化碳等卤代烃等。
加成反应条件并无特别限定,但优选为在回流下反应1~10小时。
在加成反应后,可以利用公知的方法,使用弱盐酸去除烯丙基醚基(arylether)、或利用加氢反应进行烷化。并且,也可以添加生育酚或二丁基羟基甲苯(butylated hydroxytoluene,BHT),作为抗氧化剂。
本发明的硅酮改性蜡,在25℃下为固体或具有触变性的油脂状,并且,该硅酮改性蜡的熔点可以达到40~100℃,进一步可以50~80℃。如果熔点为40℃以上,那么通常增粘效果充分,在夏季等情况下,不会引起化妆品的粘度降低或相位分离。相反,如果为100℃以下,那么不会导致化妆品中的其他成分劣化或分解,因而优选。
并且,利用凝胶渗透色谱(Gel Permeation Chromatography,GPC)测定本发明的该硅酮改性蜡的重均分子量,优选为1000~20000。
[组合物]
本发明的组合物,包含5~40质量%的上述本发明的硅酮改性蜡。由于该硅酮改性蜡将各种油剂等增粘,因此,通过与各种油剂混合,在25℃常压下,成为光滑且涂匀性良好的膏状或固体状的组合物,且与各种油剂的相溶性较高。该组合物,例如是本发明的硅酮改性蜡与后述硅酮油的混合物,除了后述化妆品以外,可以用于汽车蜡、各种脱模剂等。
[化妆品]
本发明的硅酮改性蜡(高级脂肪酸酯改性有机聚硅氧烷蜡),可以用于各种化妆品,尤其适合作为外用于皮肤或头发的化妆品的原料,例如护肤产品、美妆产品、美发产品、止汗剂产品、及防紫外线产品等。该化妆品中的该硅酮改性蜡的调配量,可以根据化妆品的种类及所调配的硅酮油的种类,在全部质量的0.5~95质量%,优选1~70质量%的范围内适当调整。例如,在乳脂状化妆品中,适合调配为全部化妆品的0.5~10质量%,优选为0.5~5质量%;在粉状体成分为全部处方的25%以下的固体状或棒状化妆品中,适合调配为全部化妆品的5~70质量%,优选为2~50质量%;并且,在粉状体成分为全部处方的80%以上的固体状化妆品中,调配为全部化妆品的1~10质量%,优选为1~5质量%。
优选为,该硅酮改性蜡是与硅酮油一起调配至化妆品中。在本说明书中,在硅酮油中,不仅包含在常温(25℃)下为液体的硅化合物,还包含将常温下为树脂状、胶状的硅树脂溶解或分散至低粘度的油剂中并成为油状的硅化合物,其中,所述油剂是例如惯用的硅酮油、烃油、及酯油等。这些硅酮油通过与上述硅酮改性蜡混合,而提供一种光滑且涂匀性良好的膏状或固体状组合物。
优选的硅酮油中包含:
(CH3)4-rSi{OSi(CH3)3}r (H)
(上式中,R5是选自由氢原子、羟基或碳数1~20的1价非取代或经过氟取代的烷基、芳基、氨取代烷基、烷氧基及由通式(CH3)3SiO{(CH3)2SiO}sSi(CH3)2CH2CH2-所表示的基团所组成的群的基团。m为0~1000的整数;1为0~1000的整数;1+m为1~1000的整数;x、y为0、1、2或3;p及q为0~8的整数,且3≤p+q≤8;r为1~4的整数;s为0~500的整数)。
在R5的一例中,可以列举:甲基、乙基、丙基、丁基、己基、辛基、癸基、十二烷基、十四烷基、十六烷基、十八烷基、三氟丙基、九氟己基、十七烷基氟癸基、苯基、氨丙基、二甲基氨丙基、氨乙基氨丙基、硬脂氧基(stearoxy)、丁氧基、乙氧基、丙氧基、十六烷氧基(cetyloxy)、十四烷氧基(myristyloxy)、苯乙烯基、及α-甲基苯乙烯基等,并包含己基、辛基、癸基、十二烷基、十四烷基、十六烷基、十八烷基、三氟丙基、苯基、氨丙基、及氨乙基氨丙基。
在硅酮油的一例中,包含:二甲基聚硅氧烷、甲基苯基聚硅氧烷、甲基氢聚硅氧烷、二甲基硅氧烷/甲基苯基硅氧烷共聚物等的从低粘度到高粘度,优选粘度为0.65~1,000,000mm2/s的常温下为液态的有机聚硅氧烷;八甲基环四硅氧烷(D4)、十甲基环五硅氧烷(D5)、十二甲基环六硅氧烷(D6)、四甲基四氢环四硅氧烷(H4)、四甲基四苯基环四硅氧烷等环状硅氧烷;三(三甲基硅氧烷基)硅烷(tris trimethyl siloxysilane,M3T)、四(三甲基硅氧烷基)硅烷(tetrakis trimethyl siloxysilane,M4Q)、及三(三甲基硅氧烷基苯基)硅烷(tristrimethyl siloxy phenyl silane)等支链硅氧烷;硬脂氧硅(stearoxy silicon)等高级 烷氧基改性硅;及,烷基改性硅、氨改性硅、及氟改性硅等。
并且,溶解或分散于低粘度油剂中所使用的硅树脂中优选的一种硅树脂,可以列举由以下方法所得的硅树脂:使烷基氢聚硅氧烷(alkyl hydrogenpolysiloxane)、与分子链中具有至少2个反应性乙烯性不饱和基团的交联剂反应,并使所得的交联型有机聚硅氧烷,经由自重以上的油剂,尤其是自重以上且粘度为0.65~10.0mm2/s的硅酮油进行膨润。作为烷基氢聚硅氧烷,可以列举:直链或具有一部分支单元的甲基氢聚硅氧烷;接枝有碳数6~20的烷基链的甲基氢聚硅氧烷;及,接枝有聚氧乙烯链的甲基氢聚硅氧烷等。键结于硅原子的氢原子,在分子中必须平均为两个以上。作为交联剂,可以列举在分子中具有两个以上的乙烯性反应部位的交联剂,例如:甲基乙烯基聚硅氧烷或α,ω-链烯二烯(alkenyl diene)、甘油三烯丙基醚(glycerin triallylether)、聚氧炔基化甘油三烯丙基醚、三羟甲基丙烷三烯丙基醚(trimethylolpropane triallyl ether)、及聚氧炔基化三羟甲基丙烷三烯丙基醚等。
进一步,优选为,此交联型有机聚硅氧烷是在交联分子中,含有选自由聚氧化烯部分、聚甘油部分、烷基部分、链烯基部分、芳基部分、及氟烷基部分所组成的群中的至少1种。作为具体例,优选日本特开平2-43263号、日本特开平2-214775号、日本专利2631772号、日本特开平9-136813号(KSG30)、日本特开2001-342255号、国际公开WO03/20828号(KSG210)、国际公开WO03/24413号(KSG40)中记载的交联型有机聚硅氧烷。通过使用此交联型有机聚硅氧烷,可以期待赋予防油脂效果、哑光质感赋予效果、粘着性提升效果、防脱色效果的特性。
作为上述交联型有机聚硅氧烷与由硅酮油、烃油、及酯油等油剂所组成的组合物的具体例,可以列举:KSG-15、KSG-16、KSG-17、KSG-18、KSG-21、KSG-210、KSG-31、KSG-32、KSG-33、KSG-34、KSG-310、KSG-320、KSG-330、KSG-340、KSG-41、KSG-42、KSG-43、KSG-44、KSG-710、KSG-810、KSG-820、KSG-830、及KSG-840(信越化学工业股份有限公司(Shin-Etsu Chemical Co.,Ltd.)制造商品名)。
溶解或分散于低粘度油剂中所使用的硅树脂中优选的第2种硅树脂,是在常温下为胶状或固体状,且优选溶解于十甲基环五硅氧烷中的硅树脂。胶状硅树脂,优选为在由通式(CH3)3SiO{(CH3)2SiO}t{(CH3)R6SiO}uSi(CH3)3所 表示的直链状硅中,R6是选自由碳数6~20的烷基、碳数3~15的含有氨基的烷基、氟取代烷基、含有季铵碱的烷基所组成的群,t为1001~20000,u为0~5000,t+u为1001~25000。
固体状硅树脂优选为硅网状化合物,所述硅网状化合物是由三烷基硅氧烷基(trialkyl siloxy)单元(M单元)、二烷基硅氧烷基单元(D单元)、单烷基硅氧烷基单元(T单元)、及4官能性硅氧烷基单元(Q单元)的任意组合所构成的MQ树脂、MDQ树脂、MTQ树脂、MDTQ树脂、TD树脂、TQ树脂、及TDQ树脂。尤其优选为,在分子中含有选自由吡咯烷酮部分、长链烷基部分、聚氧化烯部分及氟烷基部分所组成的群中的至少1部分的硅网状化合物(参照日本特开平2000-234062号、日本专利第3218872号公报)。
溶解或分散于低粘度油剂中所使用的硅树脂中优选的第3种硅树脂,是将常温下为半固体至固体状的丙烯硅(acrylic silicon)树脂溶解于挥发性硅、挥发性烃油、不挥发性硅、及不挥发性烃油中。此丙烯硅树脂尤其优选为,在分子中含有选自由吡咯烷酮部分、长链烷基部分、聚氧化烯部分及氟烷基部分所组成的群中的至少1个部分的丙烯硅树脂。这种丙烯硅树脂的结构,可以为硅链或丙烯链其中的一个为接枝状,也可以为硅链与丙烯链为嵌段状(block)(参照日本特开平1-319518号、日本专利第2704730号、日本专利第2767633号、日本专利第2767636号、及日本特开2000-344829号公报)。
在以上所述的硅酮油中,优选使用溶解于交联型二甲基聚硅氧烷、交联型聚醚改性硅、及挥发性油中的丙烯硅树脂,所述交联型二甲基聚硅氧烷、交联型聚醚改性硅、及挥发性油是利用粘度1~30mm2/s(25℃)的二甲基聚硅氧烷、十甲基环五硅氧烷、及自重以上且粘度为0.65~10.0mm2/s的硅,进行膨润而成。各种硅酮油可以单独使用或作为混合物使用。
优选为,本发明的硅酮改性蜡与硅酮油是按照1:0.01~1:45,优选为1:0.5~1:20而混合,优选包含5~40质量%的硅酮改性蜡而混合,并作为均匀的膏状、凝胶状、或固体状组合物,调配至化妆品中。全部化妆品中的硅酮油的调配量,可以根据化妆品的种类适当调整,典型为1~70质量%,优选为3~60质量%的范围。在此,硅酮油的质量是还包含溶剂的量。
除了硅酮油以外,可以根据目的而向本发明的化妆品中,调配1种或2种以上的油剂。如果是用于普通的化妆品,那么还可以使用固体、半固体、 液态、及任意的油剂。作为这种油剂的一例,可以列举:天然动植物油脂类及半合成油脂、烃油、高级醇油剂、及酯油。
例如,作为天然动植物油脂类及半合成油脂,可以列举:鳄梨油(avocadooil)、亚麻籽油(flaxseed oil)、扁桃仁油(almond oil)、昆虫蜡(Insects wax)、苏子油(perilla oil)、橄榄油(olive oil)、可可脂(cacao butter)、木棉蜡(kapok wax)、椰籽油(kaya oil)、巴西棕榈蜡(carnauba wax)、肝油(cod-liver oil)、小烛树蜡(candelilla wax)、牛脂(beef tallow)、牛蹄油(neats-foot oil)、牛骨脂(beef bonefat)、硬化牛脂、杏仁油(apricot kernel oil)、鲸蜡(spermaceti)、硬化油(hydrogenated oil)、麦胚油(wheat germ oil)、芝麻油(sesame oil)、稻米胚芽油(rice germ oil)、米糠油(rice bran oil)、甘蔗蜡(sugarcane wax)、山茶油(sasanquaoil)、红花油(safflower oil)、乳木果油(shea butter)、桐油(chinese wood oil)、肉桂油(cinnamon oil)、霍霍巴蜡(jojoba wax)、虫胶蜡(shellac wax)、海龟油(turtle oil)、大豆油(soybean oil)、茶籽油(tea seed oil)、椿油(camellia oil)、月见草油(evening primrose oil)、玉米油(corn oil)、猪油、菜子油(rapeseed oil)、日本桐油、糠蜡、胚油(germ oil)、马脂(horse fat)、桃仁油(persic oil)、棕榈油(palm oil)、棕榈核油、蓖麻油、硬化蓖麻油、蓖麻油脂肪酸甲酯、向日葵油、葡萄油、杨梅蜡(bayberry wax)、霍霍巴油、澳洲坚果油(macadamia nut oil)、蜂蜡、貂油(mink oil)、棉籽油(cottonseed oil)、棉蜡、木蜡、木蜡核油、褐煤蜡(montan wax)、椰子油(cocoanut oil)、硬化椰子油、椰子油脂肪酸三甘油酯、羊油(mutton tallow)、花生油、羊毛脂、液态羊毛脂、还原羊毛脂、羊毛脂醇(lanolin alcohol)、硬质羊毛脂、乙酸羊毛脂、羊毛脂脂肪酸异丙酯、月桂酸己酯、POE羊毛脂醇醚、POE羊毛脂醇乙酸酯(lanolin alcohol acetate)、羊毛脂脂肪酸聚乙二醇、POE加氢羊毛脂醇醚、及蛋黄油等。其中,POE代表聚氧乙烯。
作为烃油,可以列举:地蜡、角鲨烷(squalane)、鲨烯(squalene)、纯白地蜡、石蜡(paraffin)、固体石蜡(paraffin wax)、聚乙烯蜡(polyethylene wax)、聚乙烯-聚丙烯共聚物、液体石蜡(liquid faraffin)、姥鲛烷(pristane)、聚异丁烯、微晶蜡(microcrystalline wax)、及矿脂等;作为高级脂肪酸,可以列举:月桂酸、肉豆蔻酸、棕榈酸、硬脂酸、山嵛酸、十一碳烯酸、油酸、亚油酸、亚麻酸、花生四烯酸、二十碳五烯酸(eicosapentaenoic acid,EPA)、二十二碳六 烯酸(docosahexaenoic acid,DHA)、异硬脂酸、及12-羟基硬脂酸等。
作为高级醇,可以列举:月桂醇、肉豆蔻醇、棕榈醇、硬脂醇、山嵛醇、十六醇(hexadecyl alcohol)、油醇、异硬脂醇、己基十二醇(hexyl dodecanol)、辛基十二醇、十八十六醇(cetostearyl alcohol)、2-癸基四癸醇(decyltetradecynol)、胆固醇、植物甾醇、POE胆固醇醚、单硬脂酰甘油醚(鲨肝醇)、及单油基甘油醚(沙油醇)等。
作为酯油,可以列举:己二酸二异丁酯、己二酸2-己基癸酯、己二酸二-2-庚基十一烷酯、N-烷基乙二醇单异硬脂酸酯、异鲸蜡醇异硬脂酸酯、三羟甲基丙烷三异硬脂酸酯、异壬酸异十三烷酯、异壬酸异壬酯、双-2-乙基己酸乙二醇酯、鲸蜡醇2-乙基己酸酯、三羟甲基丙烷三-2-乙基己酸酯、季戊四醇四-2-乙基己酸酯、辛酸鲸蜡醇酯、辛基十二基胶酯、油醇油酸酯、辛基十二醇油酸酯、癸基油酸酯、新戊二醇二癸酸酯(neopentyl glycol dicaprate)、柠檬酸三乙酯(triethyl citrate)、琥珀酸2-乙基己酯(2-ethyethyl hexyl succinate)、醋酸戊酯(amyl acetate)、醋酸乙酯(acetic ether)、醋酸丁酯、异鲸蜡醇硬脂酸酯、硬脂酸丁酯(butyl stearate)、癸二酸二异丙酯(diisopropyl sebacate)、癸二酸二2-乙基己酯、鲸蜡醇乳酸酯、肉豆蔻乳酸酯、棕榈酸异丙酯、棕榈酸2-乙基己酯、棕榈酸2-己基癸酯、棕榈酸2-庚基十一烷酯、胆甾醇12-羟基硬脂酰酸酯、二季戊四醇脂肪酸酯、肉豆蔻酸异丙酯、肉豆蔻酸辛基十二烷酯、肉豆蔻酸2-己基癸酯、肉豆蔻酸肉豆蔻酯、二甲基辛酸己基癸酯、月桂酸乙酯、月桂酸己酯、2-辛基十二醇N-月桂酰-L-谷氨酸酯、及二异硬脂醇苹果酸酯等;作为甘油酯油,可以列举:乙酰甘油酯、三异辛酸甘油酯、三异硬脂酸甘油酯、三异棕榈酸甘油酯、单硬脂酸甘油酯、二-2-庚基十一酸甘油酯、三肉豆蔻酸甘油酯、及肉豆蔻酸异硬脂酸二甘油酯等。
作为氟系油剂,可以列举:全氟聚醚、全氟萘烷、及全氟辛烷等。
这些油剂的调配量,适合在全部化妆品的5~95质量%的范围内。尤其,化妆品的形状为固形或棒状即固体状时,适合以全部化妆品的10~50质量%的量进行调配。
在本发明的化妆品中,也可以根据目的,使用1种或2种以上的在分子结构中具有醇性羟基的化合物。作为本发明中可以添加的具有醇性羟基的化合物,有乙醇、异丙醇等低级醇;山梨糖醇、及麦芽糖等糖醇等;胆固醇、 谷甾醇、植物甾醇、羊毛甾醇等甾醇;及,丁二醇、丙二醇、二丁二醇、及戊二醇等多元醇等。作为调配量,适合在全部化妆品的0.1~98质量%的范围内。
在本发明的化妆品中,也可以根据目的而调配水。所述调配量适合在全部化妆品的1~95质量%的范围内。
在本发明的化妆品中,也可以根据目的而使用1种或2种以上具有粉状体及/或着色剂的化合物。
作为粉状体,如果是普通的化妆品中所使用的粉末,那么可以使用任意的粉末,而无需考虑它的形状(球状、针状、及板状等)或粒径(烟雾状、微粒、及颜料等级等)、及粒子结构(多孔质、无孔质等)。可以列举例如:无机粉状体、有机粉状体、表面活性剂金属盐粉状体、有色颜料、珠光颜料、金属粉末颜料、及天然色素等。
作为无机粉状体的具体例,可以列举:氧化钛、氧化锆、氧化锌、氧化铈、氧化镁、硫酸钡、硫酸钙、硫酸镁、碳酸钙、碳酸镁、滑石、云母、高岭土、绢云母、白云母、合成云母、金云母、红云母、黑云母、锂云母、硅酸、无水硅酸、硅酸铝、硅酸镁、硅酸镁铝、硅酸钙、硅酸钡、硅酸锶、钨酸金属盐、羟磷灰石(hydroxyapatite)、蛭石、氢氧化铝(higilite)、膨润土、蒙脱石(montmorillonite)、锂蒙脱石、沸石、陶瓷粉、磷酸氢钙(dibasic calciumphosphate)、氧化铝、氢氧化铝、氮化硼、一氮化硼、及硅石等。
作为有机粉状体的具体例,可以列举:聚酰胺粉末、聚酯粉末、聚乙烯粉末、聚丙烯粉末、聚苯乙烯粉末、聚氨基甲酸酯粉末、苯代三聚氰胺粉末、聚甲基苯代三聚氰胺粉末、四氟乙烯粉末、聚甲基丙烯酸甲酯粉末、纤维素、丝粉(silkpowder)、尼龙粉末、尼龙12、尼龙6、具有交联二甲基硅结构的交联型硅细粉、聚甲基硅倍半氧烷的细粉、在交联型硅上键结有聚甲基硅倍半氧烷的复合粉状体、苯乙烯/丙烯酸共聚物、二乙烯基苯/苯乙烯共聚物、乙烯树脂、尿素树脂、酚醛树脂、氟树脂、硅树脂、丙烯酸树脂、密胺树脂、环氧树脂、聚碳酸脂树脂、微晶纤维粉状体、淀粉粉末、及月桂酰赖氨酸(lauroyl lysine)等。
作为表面活性剂金属盐粉状体(金属皂)的具体例,可以列举:硬脂酸锌、硬脂酸铝、硬脂酸钙、硬脂酸镁、肉豆蔻酸锌、肉豆蔻酸镁、鲸蜡醇磷 酸锌、鲸蜡醇磷酸钙、及鲸蜡醇磷酸锌钠等。
作为有色颜料的具体例,可以列举:氧化铁、氢氧化铁、及钛酸铁的无机红色颜料;γ-氧化铁等无机褐色系颜料;氧化铁黄、黄土等无机黄色系颜料;氧化铁黑、炭黑等无机黑色颜料;锰紫、钴紫等无机紫色颜料;氢氧化铬、氧化铬、氧化钴、及钛酸钴等无机绿色颜料;深蓝、群青等无机蓝色系颜料;将焦油系色素色淀化的颜料;将天然色素色淀化的颜料;及,将这些粉状体复合化的合成树脂粉状体等。
作为珠光颜料的具体例,可以列举:镀氧化钛云母、氯氧化铋(bismuthoxychloride)、镀氧化钛氯氧化铋、镀氧化钛滑石、鱼鳞箔(fish scale foil)、及镀氧化钛着色云母等;作为金属粉末颜料,可以列举:铝粉、铜粉、及不锈钢粉末等。
焦油色素为:红色3号、红色104号、红色106号、红色201号、红色202号、红色204号、红色205号、红色220号、红色226号、红色227号、红色228号、红色230号、红色401号、红色505号、黄色4号、黄色5号、黄色202号、黄色203号、黄色204号、黄色401号、蓝色1号、蓝色2号、蓝色201号、蓝色404号、绿色3号、绿色201号、绿色204号、绿色205号、橙黄色201号、橙黄色203号、橙黄色204号、橙黄色206号、及橙黄色207号等;作为天然色素,是选自胭脂红酸、紫胶酸、红花素、巴西苏木素、及番红花素(crocin)等的粉状体。
这些粉状体也可以使用将粉状体复合化的粉末或经过普通油剂、硅酮油、氟化合物、及表面活性剂等处理的粉末,根据需要可以使用一种或两种以上。并且,作为调配量,适合在全部化妆品的0.1~99质量%的范围内。尤其,作为粉末固形化妆品的调配量,适合在全部化妆品的80~99质量%的范围内。
在本发明的化妆品中,也可以根据其目的而使用1种或2种以上的表面活性剂。作为这种表面活性剂,有阴离子性、阳离子性、非离子性及两性活性剂,但并无特别限定,可以使用任何普通化妆品中所使用的表面活性剂。
如以下例示,作为阴离子性表面活性剂,可以列举:硬脂酸钠或三乙醇胺棕榈酸脂(triethanolamine palmitate)等脂肪酸皂;烷基醚羧酸(alkyl ethercarboxylate)及其盐、氨基酸与脂肪酸的聚合盐、烷基磺酸盐(alkanesulfonate)、 烯基磺酸盐(alkenesulfonate)、脂肪酸酯的磺酸盐、脂肪酸酰胺的磺酸盐、甲醛聚合系磺酸盐、烷基硫酸酯盐、第二级高级醇硫酸酯盐、烷基及烯丙基醚硫酸酯盐、脂肪酸酯的硫酸酯盐、脂肪酸烷醇酰胺的硫酸酯盐、及土耳其红油(Turkey red oil)等硫酸酯盐类;及,烷基磷酸盐、醚磷酸盐、烷基芳基醚磷酸盐、氨基磷酸盐、及N-酰基氨基酸系活性剂等;作为阳离子性表面活性剂,可以列举:烷基胺盐、聚胺及氨基醇脂肪酸衍生物等胺盐、烷基季铵盐、芳香族季铵盐、吡啶盐、及咪唑鎓盐等。
作为非离子性表面活性剂,可以列举:山梨醇酐脂肪酸酯、甘油脂肪酸酯、聚甘油脂肪酸酯、丙二醇脂肪酸酯、聚乙烯醇脂肪酸酯、蔗糖脂肪酸酯、聚氧乙烯烷基醚、聚氧丙烯烷基醚、聚氧乙烯烷基苯基醚、聚氧乙烯脂肪酸酯、聚氧乙烯山梨醇酐脂肪酸酯、聚氧乙烯山梨醇脂肪酸酯、聚氧乙烯甘油脂肪酸酯、聚氧乙烯丙二醇脂肪酸酯、聚氧乙烯蓖麻油、聚氧乙烯硬化蓖麻油、聚氧乙烯植物甾烷醇醚、聚氧乙烯植物甾醇醚、聚氧乙烯胆甾烷醇醚、聚氧乙烯胆固醇醚、聚氧化烯改性有机聚硅氧烷(参照日本专利第2137062号、日本特开平7-330907号公报)、聚甘油改性有机聚硅氧烷(参照日本特公昭62-34039号、日本专利第2613124号、日本专利第2844453号、日本特开2002-179798号公报)、聚氧化烯/烷基协同改性有机聚硅氧烷(参照日本特开昭61-90732号、日本特开平9-59386号公报)、烷醇酰胺(alkanolamide)、糖醚、及糖胺等;作为两性表面活性剂,可以列举:甜菜碱、氨基羟酸盐(aminocarboxylate)、咪唑啉(imidazoline)衍生物、及酰氨基胺(amido amine)型等。并且,作为调配量,适合为全部化妆品的0.1~20质量%,尤其优选为0.2~10质量%的范围。
进一步可以向本发明的化妆品中添加:普通的化妆品中所使用的成分、油溶性胶化剂、有机改性粘土矿物、树脂、止汗剂、紫外线吸收剂、紫外线吸收散射剂、保湿剂、防腐剂、抗菌剂、香料、盐类、抗氧化剂、pH调节剂、螯合剂(chelating agent)、清凉剂、抗炎剂、美肌用成分(美白剂、细胞赋活剂、皮肤粗糙改善剂、血液循环促进剂、皮肤收敛剂、及抗皮脂溢剂等)、维生素类、氨基酸类、核酸、荷尔蒙、包合物(clathrate)、及头发用固体化剂等。
作为油溶性胶化剂,可以列举选自以下胶化剂:硬脂酸铝、硬脂酸镁、 及肉豆蔻酸锌(zinc myristate)等金属皂;N-月桂酰-L-谷氨酸、α,γ-二-正丁胺等氨基酸衍生物;糊精棕榈酸酯、糊精硬脂酸酯、及糊精2-乙基己酸棕榈酸酯等糊精脂肪酸酯;低聚果糖硬脂酸酯、菊粉2-乙基己酸硬脂酸酯等低聚果糖脂肪酸酯;蔗糖棕榈酸酯、蔗糖硬脂酸酯等蔗糖脂肪酸酯;单亚苄基山梨醇、二亚苄基山梨醇等山梨醇的亚苄基衍生物;及,二甲基苄基十二烷基铵蒙脱石粘土、二甲基二十八烷基铵蒙脱石粘土等有机改性粘土矿物等。
作为止汗剂,可以列举选自以下止汗剂:氯化羟铝、氯化铝、倍半氯化羟铝、羟基氯化氧锆(zirconyl hydroxy chloride)、羟基氯化铝锆(aluminumzirconium hydroxyl chlorite)、及甘氨酸铝锆(aluminum zirconium glycine)络合物等。
作为紫外线吸收剂,可以列举:对氨基苯甲酸等苯甲酸系紫外线吸收剂;邻胺基苯甲酸甲酯(methyl anthranilate)等邻胺基苯甲酸系紫外线吸收剂;水杨酸甲酯(betula oil)等水杨酸系紫外线吸收剂、对甲氧基肉桂酸辛酯等肉桂酸系紫外线吸收剂;2,4-二羟基二苯甲酮等二苯甲酮系紫外线吸收剂;尿刊酸乙酯等尿刊酸系紫外线吸收剂;及,4-叔丁基-4'-甲氧基-二苯甲酰甲烷等二苯甲酰甲烷系紫外线吸收剂等;作为紫外线吸收散射剂,可以列举:微粒氧化钛、微粒含铁氧化钛、微粒氧化锌、微粒氧化铈及它们的复合物等吸收并散射紫外线的粉状体。
作为保湿剂,有甘油、山梨糖醇、丙二醇、二丙二醇(dipropylene glycol)、1,3-丁二醇、戊二醇、葡萄糖(glucose)、木糖醇、麦芽糖醇、聚乙二醇、透明质酸(hyaluronic acid)、硫酸软骨素、吡咯烷酮羧酸盐、聚氧乙烯甲基葡萄糖甙(polyoxyethylene methyl glucoside)、及聚氧化丙烯甲基葡萄糖甙等。
作为抗菌防腐剂,有对羟基苯甲酸烷酯、苯甲酸、苯甲酸钠、山梨酸、山梨酸钾、及苯氧乙醇等;作为抗菌剂,有苯甲酸、水杨酸、石炭酸、山梨酸、对羟基苯甲酸烷酯、对氯间甲酚、六氯酚、氯化苯甲烃铵(benzalkoniumchloride)、氯化洗必泰(chlorhexidine chloride)、三氯碳酰苯胺(trichlorocarbanilide)、感光素、及苯氧乙醇等。
作为抗氧化剂,可以列举:生育酚、丁基羟基茴香醚、二丁基羟基甲苯、及植酸(phytic acid)等;作为pH调节剂,可以列举:乳酸、柠檬酸、乙醇酸(glycolic acid)、琥珀酸、酒石酸、d1-苹果酸、碳酸钾、碳酸氢钠、及碳酸氢 铵等;作为螯合剂,可以列举:丙氨酸、依地酸钠盐、聚磷酸钠、偏磷酸钠、及磷酸等;作为清凉剂,可以列举:L-薄荷醇、及樟脑等;作为抗炎剂,可以列举:尿囊素(allantoin)、甘草酸及其盐、甘草次酸及甘草次酸硬脂酰、氨甲环酸(tranexamic acid)、及甘菊环等。
作为美肌用成分,可以列举:胎盘提取液、熊果苷、谷胱甘肽、及虎耳草提取物等美白剂;蜂王浆、感光素、胆固醇衍生物、及幼牛血液提取液等细胞赋活剂、皮肤粗糙改善剂;壬酸香草基酰胺、烟酸苄酯、烟酸β-丁氧基乙酯、辣椒素、姜油酮、斑蝥酊(cantharides tincture)、鱼石脂、咖啡因、丹宁酸、α-龙脑、生育酚烟酸酯、六烟酸肌醇酯(inositol hexanicotinate)、环扁桃酯、肉桂苯哌嗪(cinnarizine)、苯甲唑啉(tolazoline)、乙酰胆碱、维拉帕米(verapamil)、西法安生(cepharanthine)、及γ-谷维素(orizanol)等血液循环促进剂;氧化锌、丹宁酸等皮肤收敛剂;及,硫、二甲硫蒽(thianthol)等抗皮脂溢剂等。作为维生素群,有维生素A油、视黄醇、醋酸视黄醇、及棕榈酸视黄醇等维生素A类;核黄素、丁酸核黄素(riboflavin butyrate)、及黄素腺嘌呤二核苷酸(flavin adenine dinucleotide)等维生素B2类、吡哆醇盐酸盐(pyridoxinehydrochloride)、吡哆素二辛酸酯(pyridoxine dioctanoate)、及吡哆素三棕榈酸酯等维生素B6类、维生素B12及其衍生物、维生素B15及其衍生物等维生素B类;L-抗坏血酸、L-抗坏血酸棕榈酸酯、L-抗坏血酸-2-硫酸钠、及L-抗坏血酸磷酸二酯二钾等维生素C类;维生素D2(ergocalciferol)、维生素D3(cholecalciferol)等维生素D类;α-生育酚、β-生育酚、γ-生育酚、醋酸d1-α-生育酚、烟酸d1-α-生育酚、及琥珀酸d1-α-生育酚等维生素E类;维生素H;维生素P;烟酸、烟酸苄酯、及烟酰胺等烟酸类;泛酸钙、D-泛醇、泛酸醇乙基醚(pantothenyl ethyl ether)、及乙酰基泛酸醇乙基醚等泛酸类;及,生物素(biotin)等。
作为氨基酸类,可以列举:氨基酸、缬氨酸、白氨酸(leucine)、异白氨酸、丝氨酸、苏氨酸、苯丙氨酸(phenylalanine)、精氨酸、赖氨酸、天冬氨酸(asparagine)、谷氨酸、胱氨酸、半胱氨酸、蛋氨酸、及色氨酸等;作为核酸,可以列举脱氧核糖核酸(deoxyribonucleic acid)等;作为荷尔蒙,可以列举雌二醇、及乙炔基雌二醇(ethinylestradiol)等。
作为头发固定用高分子化合物,可以列举:两性、阴离子性、阳离子性、 及非离子性的各种高分子化合物;可以列举:聚乙烯吡咯烷酮、乙烯吡咯烷酮/乙酸乙烯酯共聚物等聚乙烯吡咯烷酮系高分子化合物;甲基乙烯基醚/马来酸酐烷基半酯共聚物等酸性乙烯醚系高分子化合物;乙酸乙烯酯/巴豆酸共聚物等酸性聚乙酸乙烯酯系高分子;(甲基)丙烯酸/烷基(甲基)丙烯酸酯共聚物、(甲基)丙烯酸/烷基(甲基)丙烯酸酯/烷基丙烯酰胺共聚物等酸性丙烯酸系高分子化合物;及,N-甲基丙烯酰乙基-N、N-二甲基铵/α-N-甲基羧基甜菜碱/烷基(甲基)丙烯酸酯共聚物、羟基丙基(甲基)丙烯酸酯/丁基氨基乙基甲基丙烯酸酯(butyl amino ethyl methacrylate)/丙烯酸辛基酰胺共聚物等两性丙烯酸系高分子化合物。并且,也可以适当地使用纤维素或其衍生物、角蛋白及胶原质或其衍生物等源自天然的高分子化合物。
在本发明的化妆品中,包含:化妆水、乳液、面霜、洁肤霜、面膜、液体油(oil liquid)、按摩材料、洗洁剂、除臭剂、护手霜、及润唇膏等护肤化妆品;妆前底霜、扑面粉、粉底液、油性粉底、胭脂、眼影、睫毛膏、眼睑膏、眉笔、及口红等美妆化妆品;洗发水、护发素、护理液、及定型剂等头发化妆品;及,止汗剂、防晒乳或防晒霜等防紫外线化妆品等。
并且,作为这些化妆品的形状,可以选择:液态、乳液状、乳脂状、固体状、膏状、凝胶状、粉末状、按压状、多层状、摩丝状、喷雾状、棒状、及铅笔状等各种形态,尤其优选固体状或棒状。
[实施例]
以下示出合成实施例、合成比较例、实施例及比较例,更具体地说明本发明,但本发明并不限定于此。而且,在本说明书中,Me表示甲基,Bu表示丁基。
(合成实施例1)
在三颈烧瓶中,装入下述结构的甘油单烯丙基醚(glycerin mono allylether)1.0摩尔、山嵛酸2.0摩尔,以0.05质量%的对甲基苯磺酸作为催化剂,在氮气流下,以温度190℃,进行10小时的酯化反应。之后,加入碳酸氢钠水溶液作为中和剂,以温度70℃进行1小时中和反应,冷却后,使它溶解于四氢呋喃,过滤后,去除溶剂。作为所获得的酯化反应生成物的硅改性,将异丙醇作为溶剂,加入下述结构的甲基氢有机聚硅氧烷,并加入0.2质量% 的氯铂酸的10%乙醇溶液作为催化剂,在氮气流下,以温度100℃进行8小时的加成反应,得到生成物。
甘油单烯丙基醚:
甲基氢有机聚硅氧烷:
(合成实施例2)
在三颈烧瓶中,装入甘油单烯丙基醚1.0摩尔、山嵛酸2.0摩尔,以0.05质量%的对甲基苯磺酸作为催化剂,在氮气流下,以温度190℃,进行10小时的酯化反应。之后,加入碳酸氢钠水溶液作为中和剂,以温度70℃进行1小时中和反应,冷却后,使它溶解于四氢呋喃,过滤后,去除溶剂。作为所获得的酯化反应生成物的硅改性,将异丙醇作为溶剂,加入下述结构的甲基氢有机聚硅氧烷,并加入0.2质量%的氯铂酸的10%乙醇溶液作为催化剂,在氮气流下,以温度100℃进行8小时的加成反应,得到生成物。
甲基氢有机聚硅氧烷:
(合成实施例3)
在三颈烧瓶中,装入甘油单烯丙基醚1.0摩尔、山嵛酸2.0摩尔,以0.05质量%的硫酸铁n水合物作为催化剂,在氮气流下,以温度190℃,进行10小时的酯化反应。之后,使它溶解于四氢呋喃,过滤后,去除溶剂。作为所获得的酯化反应生成物的硅改性,将异丙醇作为溶剂,加入下述结构的甲基氢有机聚硅氧烷,并加入0.2质量%的氯铂酸的10%乙醇溶液作为催化剂,在氮气流下,以温度100℃进行8小时的加成反应,得到生成物。
甲基氢有机聚硅氧烷:
(合成实施例4)
在三颈烧瓶中,装入甘油单烯丙基醚1.0摩尔、山嵛酸2.0摩尔,以0.05质量%的对甲基苯磺酸作为催化剂,在氮气流下,以温度190℃,进行10小时的酯化反应。之后,加入碳酸氢钠水溶液作为中和剂,以温度70℃进行1小时中和反应,冷却后,使它溶解于四氢呋喃,过滤后,去除溶剂。作为所获得的酯化反应生成物的硅改性,将异丙醇作为溶剂,加入下述结构的甲基氢有机聚硅氧烷,并加入0.2质量%的氯铂酸的10%乙醇溶液作为催化剂,在氮气流下,以温度100℃进行8小时的加成反应,得到生成物。
甲基氢有机聚硅氧烷:
(合成实施例5)
在三颈烧瓶中,装入下述结构的三甘油单烯丙基醚(triglycerin mono allylether)1.0摩尔、山嵛酸4.0摩尔,以0.05质量%的对甲基苯磺酸作为催化剂, 在氮气流下,以温度190℃,进行10小时的酯化反应。之后,加入碳酸氢钠水溶液作为中和剂,以温度70℃进行1小时中和反应,冷却后,使它溶解于四氢呋喃,过滤后,去除溶剂。作为所获得的酯化反应生成物的硅改性,将异丙醇作为溶剂,加入下述结构的甲基氢有机聚硅氧烷,加入0.2质量%的氯铂酸的10%乙醇溶液作为催化剂,在氮气流下,以温度100℃进行8小时的加成反应,得到生成物。
三甘油单烯丙基醚:
甲基氢有机聚硅氧烷:
(合成实施例6)
在三颈烧瓶中,装入下述结构的三甘油单烯丙基醚1.0摩尔、山嵛酸3.0摩尔,以0.05质量%的对甲基苯磺酸作为催化剂,在氮气流下,以温度190℃,进行10小时的酯化反应。之后,加入碳酸氢钠水溶液作为中和剂,以温度70℃进行1小时中和反应,冷却后,使它溶解于四氢呋喃,过滤后,去除溶剂。作为所获得的酯化反应生成物的硅改性,将异丙醇作为溶剂,加入下述结构的甲基氢有机聚硅氧烷,加入0.2质量%的氯铂酸的10%乙醇溶液作为催化剂,在氮气流下,以温度100℃进行8小时的加成反应,得到生成物。
三甘油单烯丙基醚:
甲基氢有机聚硅氧烷:
(合成比较例1)
在三颈烧瓶中,装入甘油单烯丙基醚1.0摩尔、山嵛酸2.0摩尔,以0.05质量%的对甲基苯磺酸作为催化剂,在氮环境下,以温度190℃搅拌10小时而进行酯化反应。之后,加入碳酸氢钠水溶液作为中和剂,以70℃搅拌1小时,使它溶解于四氢呋喃,进行过滤,去除溶剂。
增粘剂对油剂的相溶性与组合物的评价
为了评价合成实施例1至合成实施例6、比较例1对各种油剂的相溶性,相对于各种油剂9g,添加各增粘剂1g,以80℃加热溶解,在室温中冷却后,评价组合物的状态。
相溶性的评价如下所述。
○:溶解,△:轻微浑浊,×不溶
表1
二甲基聚硅氧烷是信越化学工业(股)制造的KF-96-2cs、6cs、20cs。
增粘效果的评价如下所述。
◎:固化,〇:增粘,△:部分分离,×分离
表2
如表1、表2所示,合成实施例1至合成实施例6的增粘剂对不挥发性硅酮油的相溶性较高,使其增粘或固化。与此相对,合成比较例1的增粘剂与硅酮油的相溶性较低,油剂涌出,未能获得充分的增粘效果。
使用合成实施例1至合成实施例5、比较例1的增粘剂,制成化妆品,并进行评价。
(实施例1)乳液
(成分) 质量(%)
1.合成实施例1中所获得的硅酮改性蜡 2.0
2.二甲基聚硅氧烷2cs 30.0
3.十甲基环五硅氧烷 10.0
4.三辛酸甘油酯 5.0
5.聚醚改性硅(注1) 5.0
6.1,3-丁二醇 5.0
7.防腐剂 适量
8.香料 适量
9.纯净水 43.0
(注1)信越化学工业(股)制造:KF-6017(商品名)
(制造方法)
(A)加热溶解成分1至成分5。
(B)混合成分6至成分7及成分9后,加入上述(A)进行乳化。
(C)冷却上述(B),加入成分8,从而获得乳液。
如以上方式所获得的本发明物乳液,无粘性,且涂匀性良好。并且,当涂到皮肤上时,有光泽。
(实施例2)油包水型面霜
(成分) 质量(%)
1.角鲨烷 10.0
2.十甲基环五硅氧烷 7.0
3.二甲基聚硅氧烷2cs 5.0
4.聚醚改性分支型硅(注1) 2.0
5.合成实施例2中所获得的硅酮改性蜡 1.0
6.二丙二醇 7.0
7.防腐剂 适量
8.香料 适量
9.纯净水 68.0
(注1)信越化学工业(股)制造:KF-6028(商品名)
(制造方法)
(A)加热混合成分1至成分5。
(B)混合成分6至成分9,加入至上述(A)中,并搅拌进行乳化。
如以上方式所获得的本发明物油包水型面霜,无粘性,且涂匀性良好。
(实施例3)油包水型面霜
(成分) 质量(%)
1.合成实施例3中所获得的硅酮改性蜡 2.0
2.二甲基聚硅氧烷6cs 10.0
3.交联型聚醚改性硅(注1) 5.0
4.二丙二醇 10.0
5.柠檬酸钠 0.2
6.乙醇 5.0
7.防腐剂 适量
8.香料 适量
9.纯净水 67.8
(注1)信越化学工业(股)制造:KSG-21(商品名)
(制造方法)
(A)加热溶解成分1至成分3。
(B)混合溶解成分4至成分9,加入至上述(A)中,并搅拌进行乳化。
如以上方式所获得的本发明物油包水型面霜,不油腻,无粘性,且涂匀性良好。并且,有哑光质感。
(实施例4)油包水型妆前底霜
(成分) 质量(%)
1.交联型聚醚改性硅(注1) 4.0
2.交联型二甲基聚硅氧烷(注2) 1.0
3.聚醚改性硅(注3) 0.5
4.二甲基聚硅氧烷(6mm2/秒(25℃)) 6.0
5.二甲基聚硅氧烷(20mm2/秒(25℃)) 2.0
6.十甲基环五硅氧烷 3.0
7.氧化钛/环五硅氧烷分散物(注4) 10.0
8.合成实施例2中所获得的硅酮改性蜡 1.0
9.二丙二醇 5.0
10.柠檬酸钠 0.2
11.甲基纤维素(2%水溶液)(注5) 2.5
12.乙醇 3.0
13.防腐剂 适量
14.香料 适量
15.纯净水 61.8
(注1)信越化学工业(股)制造:KSG-21(商品名)
(注2)信越化学工业(股)制造:KSG-15(商品名)
(注3)信越化学工业(股)制造:KF-6017(商品名)
(注4)信越化学工业(股)制造:SPD-T1S(商品名)
(注5)信越化学工业(股)制造:METOLOSE 65-SH4000(商品名)
(制造方法)
(A)加热混合成分1至成分8。
(B)混合溶解成分9至成分15,加入至上述(A)中,并搅拌进行乳化。
如以上方式所获得的本发明物油包水型妆前底霜,不油腻,无粘性,且涂匀性良好。进一步,具有水润清爽的可用性,有哑光质感。
(实施例5)水包油型面霜
(成分) 质量(%)
1.合成实施例4中所获得的硅酮改性蜡 2.0
2.交联型二甲基聚硅氧烷(注1) 15.0
3.十甲基环五硅氧烷 10.0
4.二甲基聚硅氧烷20cs 18.0
5.聚醚改性硅(注2) 0.7
6.丙二醇 3.0
7.聚丙烯酰胺系混合物(注3) 0.8
8.黄原胶(2%水溶液) 8.0
9.防腐剂 适量
10.香料 适量
11.纯净水 42.5
(注1)信越化学工业(股)制造:KSG-16(商品名)
(注2)信越化学工业(股)制造:KF-6011(商品名)
(注3)SEPIC制造:SEPIGEL 305(商品名)
(制造方法)
(A)加热混合成分1至成分4。
(B)混合溶解成分5至成分11。
(C)将上述(A)加入至上述(B)中,并搅拌进行乳化。
可知如以上方式所获得的本发明物水包油型面霜,具有涂抹轻薄、清爽的可用性,是优异的水包油型面霜。
(实施例6)油包水型固状面霜
(成分) 质量(%)
1.合成实施例2中所获得的硅酮改性蜡 30.0
2.二甲基聚硅氧烷20cs 24.0
3.十甲基环五硅氧烷 24.0
4.聚醚改性硅(注1) 2.0
5.1,3-丁二醇 2.0
6.防腐剂 适量
7.香科 适量
8.纯净水 18.0
(注1)信越化学工业(股)制造:KF-6017(商品名)
(制造方法)
(A)加热溶解成分1至成分4。
(B)混合溶解成分5至成分8,加入至上述(A)中,并搅拌进行乳化。
(C)填充上述(B)作为制品。
如以上方式所获得的本发明物油包水型固状面霜,虽然油剂较多,但并不油腻,无粘性,且涂匀性良好。
(实施例7)口红
(成分) 质量(%)
1.合成实施例1中所获得的硅酮改性蜡 35.0
2.聚乙烯蜡 5.0
3.角鲨烷 30.0
4.十甲基环五硅氧烷 26.0
5.丙烯硅树脂(注1) 4.0
6.颜料 适量
7.防腐剂 适量
8.香料 适量
(注1)信越化学工业(股)制造:KP-545(商品名)
(制造方法)
(A)加热溶解成分1至成分4。
(B)混合分散成分5至成分7,加入至上述(A)中并搅拌均匀。
(C)将成分8添加至上述(B)中,并填充作为制品。
如以上方式所获得的本发明物口红,不油腻,无粘性,轻质光滑且涂匀性良好。
(实施例8)粉状粉底(powder foundation)
(成分) 质量(%)
1.绢云母 40.0
2.云母 10.0
3.滑石 剩余量
4.氧化钛 10.0
5.微粒氧化钛 5.0
6.硬脂酸镁 3.0
7.颜料 4.2
8.合成实施例3中所获得的硅酮改性蜡 1.0
9.角鲨烷 3.0
10.防腐剂 适量
11.香料 适量
(制造方法)
(A)混合成分8至成分11。
(B)混合成分1至成分7后,加入上述(A)并均匀混合。
(C)将上述(B)在金属模具中压制成形,获得粉状粉底。
如以上方式所获得的本发明物粉状粉底,无粘性,且涂匀性良好。此外, 可知粉状粉底有光泽。
(实施例9)粉底霜
(成分) 质量(%)
1.交联型聚醚改性硅(注1) 4.0
2.三辛酸甘油酯 3.0
3.二异硬脂醇苹果酸酯 5.0
4.十甲基环五硅氧烷 6.0
5.合成实施例5中所获得的硅酮改性蜡 2.0
6.氟改性混合硅复合粉状体(注2) 2.5
7.颜料 8.0
8.丙烯硅树脂(注3) 5.0
9.二丙二醇 5.0
10.柠檬酸钠 0.2
11.防腐剂 适量
12.香料 适量
13.纯净水 59.3
(注1)信越化学工业(股)制造:KSG-21(商品名)
(注2)信越化学工业(股)制造:KSP-200(商品名)
(注3)信越化学工业(股)制造:KP-545(商品名)
(制造方法)
(A)加热混合成分1至成分6。
(B)混合溶解成分9至成分13,加入至上述(A)中,并搅拌进行乳化。
(C)混合成分7至成分8,加入至上述(B)中并使其均匀。
可知如以上方式所获得的本发明物粉底霜,无粘性,涂匀性良好,且有哑光质感。
(实施例10)固状粉底
(成分) 质量(%)
1.合成实施例1中所获得的硅酮改性蜡 30.0
2.聚乙烯蜡 5.0
3.二异硬脂醇苹果酸酯 32.5
4.十甲基环五硅氧烷 28.5
5.丙烯硅树脂(注1) 4.0
6.颜料 适量
7.防腐剂 适量
8.香料 适量
(注1)信越化学工业(股)制造:KP-545(商品名)
(制造方法)
(A)加热溶解成分1至成分4。
(B)混合分散成分5至成分7,加入至上述(A)中,并搅拌均匀。
(C)将成分8添加至上述(B)中,填充作为制品。
可知如以上方式所获得的本发明物固状粉底,不油腻,无粘性,且涂匀性良好。
(实施例11)油包水型粉饼(compact foundation)
(成分) 质量(%)
1.合成实施例5中所获得的硅酮改性蜡 25.0
2.小烛树蜡 5.0
3.三2-二乙基己酸甘油酯 24.0
4.十甲基环五硅氧烷 22.0
5.丙烯硅树脂(注1) 4.0
6.三甲基硅氧烷基硅酸酯(注2) 1.0
7.聚醚改性硅(注3) 2.0
8.颜料 适量
9.1,3-丁二醇 2.0
10.防腐剂 适量
11.香料 适量
12.纯净水 15.0
(注1)信越化学工业(股)制造:KP-545(商品名)
(注2)信越化学工业(股)制造:KF-7312J(商品名)
(注3)信越化学工业(股)制造:KF-6017(商品名)
(制造方法)
(A)加热溶解成分1至成分4、成分7。
(B)混合溶解成分9、成分10及成分12,加入至上述(A)中,并搅拌进行乳化。
(C)混合分散成分5、成分6及成分8,加入至上述(B)中并搅拌匀均。
(D)将成分11添加至上述(C)中,填充作为制品。
如以上方式所获得的本发明物油包水型粉饼,虽然油剂较多,但并无粘性,且涂匀性良好。
(实施例12)眼影
(成分) 质量(%)
1.绢云母 40.0
2.云母 10.0
3.滑石 剩余量
4.氧化钛 10.0
5.微粒氧化钛 5.0
6.硬脂酸镁 3.0
7.颜料 适量
8.辛基十二醇 3.0
9.三2-二乙基己酸甘油酯 8.0
10.合成实施例3中所获得的硅酮改性蜡 2.0
11.防腐剂 适量
12.香料 适量
(制造方法)
(A)加热混合成分8至成分11。
(B)混合成分1至成分7后,加入上述(A)并均匀混合。
(C)将成分12添加至上述(B)中。
可知如以上方式所获得的本发明物眼影,无粘性,且涂匀性良好,而且 有光泽。
(实施例13)眉粉
(成分) 质量(%)
1.合成实施例2中所获得的硅酮改性蜡 3.0
2.霍霍巴油 5.0
3.三辛酸甘油酯 2.0
4.硅处理云母 40.0
5.硅处理硫酸钡 15.0
6.硅处理氧化钛 10.0
7.硅处理颜料 适量
8.混合硅复合粉状体(注1) 1.5
9.球状聚甲基硅倍半氧烷粉状体(注2) 2.5
10.硅处理滑石 剩余量
11.防腐剂 适量
12.香料 适量
(注1)信越化学工业(股)制造:KSP-100(商品名)
(注2)信越化学工业(股)制造:KMP-590(商品名)
(制造方法)
(A)混合成分4至成分12,并使其均匀。
(B)混合溶解成分1至成分3,加入至上述(A)中并使其均匀。
(C)将上述(B)在金属模具中压制成形,获得眉粉。
可知如以上方式所获得的本发明物眉粉,无粘性,且涂匀性良好,而且有光泽。
(实施例14)铅笔状眉笔
(成分) 质量(%)
1.合成实施例4中所获得的硅酮改性蜡 40.0
2.聚乙烯蜡 10.0
3.霍霍巴油 40.0
4.十甲基环五硅氧烷 5.0
5.丙烯硅树脂(注1) 5.0
6.颜料 适量
7.防腐剂 适量
8.香料 适量
(注1)信越化学工业(股)制造:KP-545(商品名)
(制造方法)
(A)加热溶解成分1至成分4。
(B)混合分散成分5至成分,加入至上述(A)中并搅拌均匀。
(C)将成分8添加至上述(B)中,填充作为制品。
如以上方式所获得的本发明物铅笔状眉笔,无飞粉,光滑性优异,且涂匀性良好。
(实施例15)发膏(hair cream)
(成分) 质量(%)
1.合成实施例4中所获得的硅酮改性蜡 2.0
2.单异硬脂酸甘油酯(mono iso glyceryl stearate) 5.0
3.十甲基环五硅氧烷 8.0
4.硬脂酰三甲基氯化铵 1.5
5.甘油 3.0
6.丙二醇 5.0
7.羟乙基纤维素 0.2
8.防腐剂 适量
9.香料 适量
10.纯净水 75.3
(制造方法)
(A)加热溶解成分1至成分3。
(B)均匀地混合溶解成分4至成分8及成分10。
(C)将上述(B)加入至上述(A)中乳化后,冷却并加入成分9。
可知由于如以上方式所获得的本发明物发膏,在涂布时的涂匀性、使用 后头发的柔软性、光滑度、湿润感、光泽方面,表现出极为优异的效果,因此,综合来说非常优异。
(实施例16)调节摩丝(conditioning mousse)
(成分) 质量(%)
1.合成实施例2中所获得的硅酮改性蜡 0.5
2.单异硬脂酸甘油酯 2.0
3.交联型二甲基聚硅氧烷(注1) 0.5
4.三辛酸甘油酯 1.5
5.甘油 3.0
6.硬脂酰二甲基苄基氯化铵 0.5
7.聚氧乙烯硬化蓖麻油 0.5
8.乙醇 7.0
9.防腐剂 适量
10.香料 适量
11.纯净水 剩余量
12.液化石油气 5.0
(注1)信越化学工业(股)制造:KSG-16(商品名)
(制造方法)
(A)加热溶解成分1至成分4。
(B)均匀地混合溶解成分5至成分9及成分11。
(C)将上述(B)加入至上述(A)中乳化后,冷却并加入成分10。
(D)将上述(C)填充至气溶胶罐中,获得调节摩丝。
可知如以上方式所获得的本发明物调节摩丝,湿润感、柔软性、光滑度优异,无油腻感且有良好触感,而且有哑光质感。
(实施例17)滚搽式(roll-on type)止汗剂
(成分) 质量(%)
1.合成实施例1中所获得的硅酮改性蜡 5.0
2.交联型聚醚改性硅(注1) 20.0
3.液体石蜡 10.0
4.交联型二甲基聚硅氧烷(注2) 15.0
5.十甲基环五硅氧烷 30.0
6.铝锆四氯水合物(aluminum zirconium tetrachloro hydrate) 20.0
7.香料 适量
(注1)信越化学工业(股)制造:KSG-21(商品名)
(注2)信越化学工业(股)制造:KSG-15(商品名)
(制造方法)
(A)加热混合成分1至成分5
(B)将成分6、成分7加入至上述(A)中,均匀地分散。
如以上方式所获得的滚搽式的止汗剂,涂匀性良好,无粘性或油感,且不随温度或时间而变化,可用性与稳定性均非常优异。
(实施例18)油包水型止汗剂
(成分) 质量(%)
1.合成实施例3中所获得的硅酮改性蜡 2.0
2.交联型聚醚改性硅(注1) 7.0
3.十甲基环五硅氧烷 7.0
4.液体石蜡 8.0
5.1,3-丁二醇 5.0
6.柠檬酸钠 0.2
7.氯化铝水合物 20.0
8.香料 适量
9.纯净水 50.8
(注1)信越化学工业(股)制造:KSG-21(商品名)
(制造方法)
(A)加热混合成分1至成分4。
(B)混合成分5至成分6及成分8,加入成分7、成分8进行溶解。
(C)将上述(B)加入至上述(A)中,并搅拌进行乳化。
如以上方式所获得的油包水型的止汗剂,涂匀性良好,无粘性或油感, 且不随温度或时间而变化,可用性与稳定性均非常优异。
(实施例19)固状止汗剂
(成分) 质量(%)
1.合成实施例5中所获得的硅酮改性蜡 22.0
2.聚乙烯-聚丙烯共聚物 4.0
3.二甲基聚硅氧烷(6mm2/秒(25℃)) 22.0
4.十甲基环五硅氧烷 22.0
5.交联型二甲基聚硅氧烷(注1) 15.0
6.铝锆四氯水合物 15.0
7.香料 适量
(注1)信越化学工业(股)制造:KSG-16(商品名)
(制造方法)
(A)加热成分1至成分5使其均匀。
(B)将成分6、成分7混合分散至上述(A)中。
(C)填充上述(B)作为制品。
如以上方式所获得的固状止汗剂,涂匀性良好,无粘性或油感,且不随温度或时间而变化,可用性与稳定性均非常优异。
(实施例20)固状止汗剂
(成分) 质量(%)
1.合成实施例4中所获得的硅酮改性蜡 25.0
2.聚乙烯蜡 8.0
3.二甲基聚硅氧烷(6mm2/秒(25℃)) 25.0
4.十甲基环五硅氧烷 22.0
5.交联型二甲基聚硅氧烷(注1) 5.0
6.铝锆四氯水合物(甘氨酸盐) 15.0
7.香料 适量
(注1)信越化学工业(股)制造:KSG-16(商品名)
(制造方法)
(A)加热成分1至成分5使其均匀。
(B)将成分6、成分7混合分散至上述(A)中。
(C)填充上述(B)作为制品。
如以上方式所获得的固状止汗剂,涂匀性良好,无粘性或油感,且不随温度或时间而变化,可用性与稳定性均非常优异。
(实施例21)防紫外线油包水型面霜
(成分) 质量(%)
1.硅处理氧化锌 20.0
2.丙烯改性硅树脂(注1) 12.0
3.十甲基环五硅氧烷 20.0
4.三辛酸甘油酯 3.0
5.合成实施例2中所获得的硅酮改性蜡 2.0
6.交联型聚醚改性硅(注2) 5.0
7.聚醚改性硅(注3) 1.0
8.烷基/聚醚协同改性硅(注4) 1.0
9.甲氧基肉桂酸辛酯 6.0
10.柠檬酸钠 0.2
11.二丙二醇 3.0
12.防腐剂 适量
13.香料 适量
14.纯净水 26.8
(注1)信越化学工业(股)制造:KP-545(商品名)
(注2)信越化学工业(股)制造:KSG-21(商品名)
(注3)信越化学工业(股)制造:KF-6017(商品名)
(注4)信越化学工业(股)制造:KF-6026(商品名)
(制造方法)
(A)加热混合成分3的一部分、及成分4至成分9。
(B)混合成分10至成分12、及成分14,加入至上述(A)中,并搅拌进行乳化。
(C)混合分散成分1、成分2及成分3的剩余部分,将成分13加入至上述(B)中,并使其均匀。
如以上方式所获得的油包水型的防紫外线面霜,涂匀性良好,无粘性或油感,有透明感,且不随温度或时间而变化,可用性与稳定性均非常优异。
(实施例22)防紫外线油包水型乳液
(成分) 质量(%)
1.二甲基聚硅氧烷(6mm2/秒(25℃)) 5.0
2.交联型聚醚改性硅(注1) 5.0
3.三辛酸甘油酯 2.0
4.合成实施例3中所获得的硅蜡(C) 1.0
5.聚醚改性硅(注2) 1.0
6.氧化钛/十甲基环五硅氧烷分散物(注3) 30.0
7.氧化锌/十甲基环五硅氧烷分散物(注4) 30.0
8.二丙二醇 3.0
9.柠檬酸钠 0.2
10.防腐剂 适量
11.香料 适量
12.纯净水 22.8
(注1)信越化学工业(股)制造:KSG-21(商品名)
(注2)信越化学工业(股)制造:KF-6017(商品名)
(注3)信越化学工业(股)制造:SPD-T1S(商品名)
(注4)信越化学工业(股)制造:SPD-Z1(商品名)
(制造方法)
(A)加热混合成分1至成分5。
(B)混合溶解成分8至成分10、成分12,加入至上述(A)中,并搅拌进行乳化。
(C)将成分6、成分7、成分11加入至上述(B)中,并使其均匀。
如以上方式所获得的油包水型的防紫外线乳液,涂匀性良好,无粘性或油感,有透明感,定妆持久,且不随温度或时间而变化,可用性与稳定性均 非常优异。
(实施例23)防紫外线水包油型面霜
(成分) 质量(%)
1.交联型有机聚硅氧烷(注1) 5.0
2.鲸蜡醇异辛酸酯 5.0
3.合成实施例5中所获得的硅酮改性蜡 1.0
4.氧化钛/十甲基环五硅氧烷分散物(注2) 15.0
5.聚醚改性硅(注3) 1.0
6.聚醚改性硅(注4) 1.0
7.丙烯酸酰胺系混合物(注5) 2.0
8.丙二醇 5.0
9.甲基纤维素(2%水溶液)(注6) 5.0
10.防腐剂 适量
11.香料 适量
12.纯净水 60.0
(注1)信越化学工业(股)制造:KSG-18(商品名)
(注2)信越化学工业(股)制造:SPD-T1S(商品名)
(注3)信越化学工业(股)制造:KF-6027(商品名)
(注4)信越化学工业(股)制造:KF-6011(商品名)
(注5)SEPIC制造:SEPIGEL 305(商品名)
(注6)信越化学工业(股)制造:METOLOSE SM-4000(商品名)
(制造方法)
(A)混合成分5至成分8及成分10、成分12。
(B)加热混合成分1至成分3,加入至上述(A)中,并搅拌进行乳化。
(C)将成分4加入至上述(B)中,进一步加入成分9、成分10使其均匀。
如以上方式所获得的水包油型的防紫外线面霜,涂匀性良好,无粘性或油感,有透明感,定妆持久,且不随温度或时间而变化,可用性与稳定性均非常优异。
(比较例1)固状粉底
在实施例10中,使用合成比较例1中所获得的增粘剂,来代替成分1.硅酮改性蜡,除此以外与实施例10同样地制造固状粉底。相较于实施例10的粉底,所获得的固状粉底具有粘性,延展性较差。
另外,本发明并不限定于所述实施方式。所述实施方式为例示,具有与本发明的权利要求范围所述的技术思想实质相同的结构,并发挥相同作用效果的技术方案,均包含在本发明的技术范围内。
Claims (8)
1.一种硅酮改性蜡,其特征在于,其是通过使在1分子中具有1个或2个烯基的多元醇与高级脂肪酸发生酯化反应,并使所得生成物与含有至少1个甲基的有机氢聚硅氧烷发生氢化硅烷化反应而获得,且在25℃下为固体或具有触变性的油脂状。
3.如权利要求1所述的硅酮改性蜡,其中,前述硅酮改性蜡的熔点为40~100℃。
4.如权利要求2所述的硅酮改性蜡,其中,前述硅酮改性蜡的熔点为40~100℃。
5.一种组合物,其特征在于,其含有5~40质量%的权利要求1至4中的任一项所述的硅酮改性蜡,且在25℃常压下为膏状或固体状。
6.一种化妆品,其特征在于,其含有权利要求1至4中的任一项所述的硅酮改性蜡。
7.一种硅酮改性蜡的制造方法,其特征在于,其包括:
工序(I),在催化剂存在下,使在1分子中具有1个或2个烯基的多元醇与高级脂肪酸发生酯化反应,得到酯化反应生成物;及,
工序(II),在催化剂存在下,使前述酯化反应生成物与含有至少1个甲基的有机氢聚硅氧烷发生氢化硅烷化反应。
8.如权利要求7所述的硅酮改性蜡的制造方法,其中,
作为前述在1分子中具有1个或2个烯基的多元醇,使用具有直链或支链状聚甘油结构的化合物;
作为前述高级脂肪酸,使用碳数12~30的直链状饱和型高级脂肪酸;并且,
作为前述有机氢聚硅氧烷,使用由下述通式(A)所表示的有机氢聚硅氧烷,
式(A)中,R1、R2、R3、R4分别独立地表示氢原子、相同或不同且可以具有分支聚丙三醇链键结的连结基或取代基且碳数1~22的直链或支链的烷基或烷氧基、碳数6~22的芳基、及氟取代烷基中的任一个;其中,R1、R3中至少1个表示氢原子,R2、R4中至少1个表示甲基;n表示0~100的整数。
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- 2012-12-05 US US13/705,593 patent/US20130150458A1/en not_active Abandoned
- 2012-12-06 KR KR1020120140748A patent/KR20130064022A/ko not_active Application Discontinuation
- 2012-12-06 CN CN2012105201559A patent/CN103145995A/zh active Pending
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Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
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CN111356442A (zh) * | 2017-11-02 | 2020-06-30 | 信越化学工业株式会社 | 免冲洗护发化妆品 |
CN111356442B (zh) * | 2017-11-02 | 2023-03-14 | 信越化学工业株式会社 | 免冲洗护发化妆品 |
CN108261350A (zh) * | 2018-02-01 | 2018-07-10 | 湖南斯洛柯有机硅有限公司 | 一种乳化剂及其制备方法和含有它的化妆品 |
CN112352010A (zh) * | 2018-07-11 | 2021-02-09 | 信越化学工业株式会社 | 交联型有机硅树脂和其制造方法、以及化妆品 |
CN112352010B (zh) * | 2018-07-11 | 2023-07-14 | 信越化学工业株式会社 | 交联型有机硅树脂和其制造方法、以及化妆品 |
CN110357750A (zh) * | 2019-07-31 | 2019-10-22 | 北矿亿博(沧州)科技有限责任公司 | 乳化炸药用复合油相及其制备方法、乳化基质和乳化炸药 |
CN110357750B (zh) * | 2019-07-31 | 2021-02-26 | 北矿亿博(沧州)科技有限责任公司 | 乳化炸药用复合油相及其制备方法、乳化基质和乳化炸药 |
CN115484925A (zh) * | 2020-04-01 | 2022-12-16 | 花王株式会社 | 化妆方法 |
Also Published As
Publication number | Publication date |
---|---|
EP2602279A1 (en) | 2013-06-12 |
KR20130064022A (ko) | 2013-06-17 |
US20130150458A1 (en) | 2013-06-13 |
JP2013119596A (ja) | 2013-06-17 |
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