專利文獻1之護髮油於塗抹於洗髮後之濕潤毛髮之情形時,可賦予乾燥後之整齊感或調理效果,但塗抹於乾燥毛髮之情形時仍會出現塗抹不均,因此存在乾燥後之整齊度不充分或觸感欠佳之問題。又,若塗抹足以均勻塗覆毛髮整體之充足量,則亦存在乾燥後感覺較重或毛束感殘留之問題。 又,認為專利文獻2之分叉毛髮塗抹劑為了被覆分叉毛髮而較佳為於組合物整體中包含10~50重量%、尤其20~40重量%之二甲基聚矽氧烷衍生物。因此,乾燥後亦因大量殘留於毛髮上之二甲基聚矽氧烷衍生物導致毛髮感覺上較重或毛束感殘留,另外難以獲得乾爽之觸感。 因此,本發明係關於一種毛髮化妝料,其於塗抹於乾燥毛髮時之濕潤擴展性良好,且塗抹後即刻變乾,不會造成乾澀感或毛髮潮濕之觸感,乾燥後不會形成毛束而可使毛髮保持自然之整齊度。 本發明者等人認為上述非水系毛髮化妝料之問題主要在於乾燥毛髮上之濕潤擴展性不充分、以及塗抹後揮發性油之揮發耗費時間,對此方面展開研究。其結果發現,若將特定之矽酮油與低級醇設為特定比率,則溶劑之表面張力明顯增大,應用於毛髮上之毛髮化妝料自發地於毛髮表面移動,與此同時所含有之聚合物被覆毛髮表面。並且結果發現,可將所含有之聚合物成分快速均勻地塗抹於毛髮表面,進而極快速地乾燥,因此於塗抹後不久毛髮上之毛髮化妝料之存在感便消失,且乾燥後之毛髮保持整齊,從而完成了發明。 本發明之毛髮化妝料於乾燥毛髮之毛髮表面自發地移動且快速乾燥。因此,毛髮化妝料中之聚合物快速地輕薄且均勻地於毛髮表面擴散,塗抹後毛髮化妝料之存在感迅速消失,無不自然之毛束感,手感毫不黏膩,且賦予自然之整齊度。進而,塗抹時無乾澀感或黏膩感,亦無毛髮潮濕之觸感。 [成分(A):於水或乙醇中具有溶解性或分散性之毛髮化妝料用聚合物] 成分(A)為即便不使用界面活性劑而亦溶解或穩定地分散於水或乙醇之聚合物,且可穩定地存在於如成分(B)之具有極性之溶劑中的成分。該成分(A)係利用本發明之構成而被均勻塗抹於毛髮表面上,藉此不會感到聚合物之存在感而可對毛髮賦予自然之整齊感或自然之觸感的成分。作為此種於水或乙醇中具有溶解性或分散性之毛髮化妝料用聚合物,較佳為被膜形成聚合物或聚醚改性矽酮。 就進一步增強整齊感之觀點而言,較佳為使用被膜形成聚合物作為成分(A)。作為成分(A)所能使用之皮膜形成聚合物,只要為於水或乙醇中具有溶解性或分散性者則並無特別限定,可使用通常用於整髮劑之在定型力較高者至定型力相對較低者中之任一者。 作為此種被膜形成聚合物,可列舉:矽酮系接枝聚合物、胺基甲酸酯系高分子化合物、聚乙烯基吡咯啶酮系高分子化合物、陰離子性乙烯醚系高分子化合物、陰離子性聚乙酸乙烯酯系高分子化合物、陰離子性(甲基)丙烯酸系高分子化合物、兩性(甲基)丙烯酸系高分子化合物、非離子性(甲基)丙烯酸系高分子化合物、陽離子性(甲基)丙烯酸系高分子化合物、順丁烯二醯亞胺系高分子化合物等。 作為矽酮系接枝聚合物,可列舉:聚(N-甲醯基伸乙基亞胺)有機聚矽氧烷、聚(N-乙醯基伸乙基亞胺)有機聚矽氧烷、聚(N-丙醯基伸乙基亞胺)有機聚矽氧烷等聚矽酮-9;聚矽酮-28等國際公開第2014/002707號記載之有機聚矽氧烷接枝聚合物;KP-545(信越化學工業公司)等丙烯酸烷基酯共聚物甲基聚矽氧烷酯;Silsoft Spread TT(Momentive公司)等聚矽酮-17;Luviflex Silk(BASF公司)等丙烯酸烷基酯・甲基丙烯酸・矽酮共聚物等。該等之中,就定型性、乾燥時無黏膩感、塗抹後之柔軟度、塗抹後之梳理性之觀點而言,更佳為聚(N-甲醯基伸乙基亞胺)有機聚矽氧烷、聚(N-乙醯基伸乙基亞胺)有機聚矽氧烷、聚(N-丙醯基伸乙基亞胺)有機聚矽氧烷等聚矽酮-9;聚矽酮-28等國際公開第2014/002707號記載之有機聚矽氧烷接枝聚合物、KP-545(信越化學工業公司)等丙烯酸烷基酯共聚物甲基聚矽氧烷酯。 作為胺基甲酸酯系高分子化合物,可列舉:Luviset P.U.R.(BASF Japan公司)等聚胺基甲酸酯;DynamX(AkzoNobel公司)等聚胺基甲酸酯-14・AMP-丙烯酸酯共聚物。 作為聚乙烯基吡咯啶酮系高分子化合物,可列舉:Luviskol K12、Luviskol K17、Luviskol K30、Luviskol L60、Luviskol K80、Luviskol K90(BASF公司);PVP K15、PVP K17、PVP K30、PVP K60、PVP K90、PVP K120(以上為Ashland公司)等聚乙烯基吡咯啶酮;Luviskol VA28、Luviskol VA37、Luviskol VA55、Luviskol VA64P、Luviskol VA73(以上為BASF公司);Luviskol Plus(BASF公司)等聚乙烯基己內醯胺;PVP/VA E-735、PVP/VA E-635、PVP/VA E-535、PVP/VA E-335、PVP/VA S-630、PVP/VA W-735(以上為Ashland公司)等(乙烯基吡咯啶酮/乙酸乙烯酯)共聚物;Luviskol VAP343(BASF公司)等聚乙烯基吡咯啶酮/乙酸乙烯酯/丙酸乙烯酯三元共聚物;Luviflex(BASF公司);Copolymer 845、Copolymer 937、Copolymer 958(以上為Ashland公司)等聚乙烯基吡咯啶酮/二甲基胺基甲基/丙烯酸共聚物;Copolymer VC-713(Ashland公司)等聚乙烯基吡咯啶酮/甲基丙烯酸二甲基胺基乙酯/乙烯基己內醯胺共聚物;Luviset Clear(BASF公司)等(VP/甲基丙烯醯胺/乙烯基咪唑)共聚物;Luviquat HM552(BASF公司)等乙烯基咪唑鎓甲基氯化物/乙烯基吡咯啶酮共聚物等。該等之中,就剛塗抹後不久之順滑性、定型性、乾燥時無黏膩感、塗抹後之柔軟度之觀點而言,更佳為(乙烯基吡咯啶酮/乙酸乙烯酯)共聚物、聚乙烯基吡咯啶酮。 作為陰離子性乙烯醚系高分子化合物,可列舉:Gantrez ES-225 (Ashland公司)等(乙烯基甲醚/順丁烯二酸乙酯)共聚物;Gantrez ES-425 (Ashland公司)等(乙烯基甲醚/順丁烯二酸丁酯)共聚物等。該等之中,就定型性、乾燥時無黏膩感、塗抹後之柔軟度之觀點而言,較佳為(乙烯基甲醚/順丁烯二酸丁酯)共聚物。 作為陰離子性聚乙酸乙烯酯系高分子化合物,可列舉:Resin 28-1310 (AkzoNobel公司)、Luviset CA66(BASF公司)等乙酸乙烯酯/丁烯酸共聚物;Resin 28-2930(AkzoNobel公司)等(乙酸乙烯酯/丁烯酸/新癸酸乙烯酯)共聚物;Luviset CAP(BASF公司)等乙酸乙烯酯/丁烯酸/丙酸乙烯酯共聚物等。 作為陰離子性(甲基)丙烯酸系高分子化合物,可列舉:Plas-size L-53P、Plas-size L-9540B(以上為互應化學工業公司)等丙烯酸系樹脂烷醇胺液;Diahold(三菱化學公司)等丙烯酸/丙烯酸酯共聚物;Ultrahold 8、Ultrahold strong(以上為BASF公司)、或AMPHOMER V-42、DERMACRYL 79(以上為AkzoNobel公司)等丙烯酸/丙烯醯胺/丙烯酸乙酯共聚物;Aniset NF-1000、Aniset HS-3000(以上為大阪有機化學工業公司)等丙烯酸烷基酯共聚物等。 作為兩性(甲基)丙烯酸系高分子化合物,可列舉:Yukaformer M-75、Yukaformer R205、Yukaformer 301、Yukaformer SM(以上為三菱化學公司)、RAM Resin(大阪有機化學公司)等(甲基丙烯醯氧基乙基羧基甜菜鹼/甲基丙烯酸烷基酯)共聚物;AMPHOMER 28-4910、AMPHOMER LV-71 (以上為AkzoNobel公司)等(辛基丙烯醯胺/丙烯酸羥基丙酯/甲基丙烯酸丁基胺基乙酯)共聚物;AMPHOMER HC(AkzoNobel公司)等(丙烯酸烷基酯/辛基丙烯醯胺)共聚物;DIAFORMER Z-651(三菱化學公司)等之(丙烯酸酯/丙烯酸月桂酯/丙烯酸硬脂酯/甲基丙烯酸乙基氧化胺)共聚物等。該等之中,就定型性、乾燥時無黏膩感、塗抹後之柔軟度之觀點而言,較佳為(甲基丙烯醯氧基乙基羧基甜菜鹼/甲基丙烯酸烷基酯)共聚物。 作為非離子性(甲基)丙烯酸系高分子化合物,可列舉:Plas-size L-2700、Plas-size L-2714(以上為互應化學工業公司)等(二甲基丙烯醯胺/丙烯酸羥基乙酯/丙烯酸甲氧基乙酯)共聚物等。 作為陽離子性(甲基)丙烯酸系高分子化合物,可列舉:日本專利特開平2-180911號公報記載之烷基丙烯醯胺/丙烯酸酯/烷基胺基烷基丙烯醯胺/聚乙二醇甲基丙烯酸酯共聚物;日本專利特開平8-291206號公報記載之烷基丙烯醯胺/烷基胺基烷基丙烯醯胺/聚乙二醇甲基丙烯酸酯共聚物;Plas-size L-515(互應化學工業公司)等聚四級銨鹽-99;Aquaflex SF-40(Ashland公司)等(PVP/乙烯基己內醯胺/丙烯酸DMAPA)共聚物;STYLEZE CC-10(Ashland公司)等(乙烯基吡咯啶酮/丙烯酸DMAPA)共聚物;Luviquat PQ11(BASF公司)、GAFQUAT 734、GAFQUAT 755(以上為Ashland公司)等乙烯基吡咯啶酮/二甲基胺基甲基丙烯酸酯共聚物之四級化物(聚四級銨鹽-11)。其中,較佳為日本專利特開平2-180911號公報記載之烷基丙烯醯胺/丙烯酸酯/烷基胺基烷基丙烯醯胺/聚乙二醇甲基丙烯酸酯共聚物、日本專利特開平8-291206號公報記載之烷基丙烯醯胺/烷基胺基烷基丙烯醯胺/聚乙二醇甲基丙烯酸酯共聚物、聚四級銨鹽-11。 作為順丁烯二醯亞胺系高分子化合物,可列舉Aquaflex FX-64(ISP Japan公司)等(異丁烯/乙基順丁烯二醯亞胺/羥基乙基順丁烯二醯亞胺)共聚物。 該等被膜形成聚合物之中,就定型性、乾燥時無黏膩感、塗抹後之柔軟度之觀點而言,更佳為矽酮系接枝聚合物、聚乙烯基吡咯啶酮系高分子化合物、陰離子性聚乙酸乙烯酯系高分子化合物、兩性(甲基)丙烯酸系高分子化合物、非離子性(甲基)丙烯酸系高分子、陽離子性(甲基)丙烯酸系化合物。 另一方面,就剛塗抹後不久無乾澀感、進一步提高乾燥後之整齊度之觀點而言,較佳為使用聚醚改性矽酮作為成分(A)。作為成分(A)所能使用之聚醚改性矽酮,只要為於水或乙醇中具有溶解性或分散性者則並無特別限定,可列舉:聚氧乙烯改性矽酮、聚丙烯改性矽酮、聚氧乙烯/聚氧丙烯改性矽酮、聚甘油改性矽酮等,作為改性之形式,可列舉側鏈型(側鏈改性型)與直鏈共聚合型等。 作為此種聚醚改性矽酮,較佳為具有有機矽氧烷鏈與聚伸烷基鏈之嵌段鏈之共聚物,可列舉:Silsoft A+(Momentive公司)等(PEG-40/PPG-8甲基胺基丙基/羥基丙基二甲聚矽氧烷)共聚物;FZ-2222、FZ-2233、CB2250(Dow Corning Toray公司)等聚矽酮-13;Silwet L-8600(Momentive公司)等PEG-12二甲聚矽氧烷、Silsoft 900(Momentive公司)等PPG-12二甲聚矽氧烷;Silsoft 860(Momentive公司)等PEG-10二甲聚矽氧烷;SILSTYLE 104(Dow Corning Toray公司)等(雙異丁基PEG-14/胺基二甲聚矽氧烷)共聚物;SILSTYLE 401(Dow Corning Toray公司)等(雙異丁基PEG/PPG-20/35/胺基二甲聚矽氧烷)共聚物;CE-8411 Smooth Plus Emulsion(Dow Corning Toray公司)等雙-異丙醇胺基-PG-丙基二甲聚矽氧烷/雙異丁基PEG-14共聚物;DOW CORNING TORAY SS-3588(Dow Corning Toray公司)等(雙異丁基PEG-15/胺基二甲聚矽氧烷)共聚物等。其中,較佳為具有胺基改性有機聚矽氧烷鏈與聚氧伸烷基鏈之嵌段鏈之共聚物,更佳為(雙異丁基PEG-14/胺基二甲聚矽氧烷)共聚物、(雙異丁基PEG/PPG-20/35/胺基二甲聚矽氧烷)共聚物、雙-異丙醇胺基-PG-丙基二甲聚矽氧烷/雙異丁基PEG-14共聚物、(雙異丁基PEG-15/胺基二甲聚矽氧烷)共聚物之類的直鏈共聚合型胺基・聚醚改性矽酮,進而較佳為(雙異丁基PEG-15/胺基二甲聚矽氧烷)共聚物。 該等毛髮化妝料用聚合物可單獨使用任一者或將2種以上組合使用,就進一步提高自然之整齊感與自然之觸感兩者之觀點而言,較佳為將上述被膜形成聚合物與聚醚改性矽酮一併用作成分(A)。 又,就乾燥時不會產生黏膩感而輕薄且均勻地殘留於毛髮上、更進一步賦予自然之觸感與整齊度之觀點而言,成分(A)較佳為兩親媒性被膜形成性高分子或聚醚改性矽酮。所謂兩親媒性被膜形成性高分子係以質量比計包含10~98%之疏水部之定型聚合物,作為此種兩親媒性定型聚合物,可列舉:聚矽酮-9、聚矽酮-28,尤佳為聚矽酮-9。 關於本發明之毛髮化妝料中之成分(A)之含量,就賦予毛髮之整齊性之觀點而言為0.1質量%以上,較佳為0.5質量%以上,更佳為1質量%以上。又,就不會使毛髮感覺較重或不會造成毛束感、賦予自然之觸感與整齊感之觀點而言為10質量%以下,較佳為7質量%以下,更佳為5質量%以下。 [成分(B):碳數1~4之一元醇] 成分(B)係藉由與成分(C)加以組合而控制包含成分(A)之毛髮化妝料之濕潤擴展性、及毛髮上之乾燥速度的成分。作為成分(B)之碳數1~4之一元醇,可使用飽和或不飽和之脂肪族醇。該等一元醇可單獨使用1種或將2種以上組合使用。作為醇,較佳為乙醇、丙醇、異丙醇、第三丁醇,更佳為乙醇、異丙醇,進而較佳為乙醇。 關於本發明之毛髮化妝料中之成分(B)之含量,就乾燥速度、無束感之觀點而言,較佳為45質量%以上,更佳為55質量%以上,進而較佳為60質量%以上,又,就塗抹後無乾澀感之觀點而言,較佳為98質量%以下,更佳為90質量%以下,更佳為80質量%以下,進而較佳為75質量%以下。 [成分(C):數量平均分子量為100以上且1500以下之矽酮] 成分(C)為數量平均分子量100以上且1500以下之矽酮,且係藉由與成分(B)加以組合而控制毛髮化妝料之濕潤擴展性及毛髮化妝料於毛髮上之乾燥速度的成分。作為此種矽酮,例如可列舉:八甲基環四矽氧烷、十甲基環五矽氧烷、十二甲基環六矽氧烷、甲基環聚矽氧烷等環狀矽酮;八甲基三矽氧烷、十四甲基六矽氧烷、甲基三甲聚矽氧烷、25℃下之動黏度例如為0.5 mm2
/s以上且10 mm2
/s以下之甲基聚矽氧烷等鏈狀矽酮等。其中,較佳為十甲基環五矽氧烷、甲基三甲聚矽氧烷、25℃下之動黏度為0.5 mm2
/s以上且未達6 mm2
/s之甲基聚矽氧烷等鏈狀矽酮,更佳為十甲基環五矽氧烷、甲基三甲聚矽氧烷。 關於成分(C)之數量平均分子量,就塗抹後良好之順滑性、梳理性之觀點而言,較佳為100以上,更佳為150以上,更佳為200以上。又,就乾燥後無毛束感且感覺輕盈之觀點而言,較佳為1000以下,更佳為700以下,更佳為500以下。 又,就乾燥後之輕盈感或劑無存在感之觀點而言,成分(C)較佳為揮發性矽酮。所謂揮發性矽酮係WHO(世界衛生組織)所規定之高揮發性有機化合物、揮發性有機化合物,且沸點為260℃以下之矽酮。又,作為揮發性矽酮,較佳為沸點為50℃以上者。 關於本發明之毛髮化妝料中之成分(C)之含量,就塗抹後良好之順滑性、梳理性之觀點而言,較佳為1質量%以上,更佳為10質量%以上,進而較佳為20質量%以上,進而較佳為25質量%以上,又,就乾燥後無毛束感且感覺輕盈之觀點而言,較佳為52質量%以下,更佳為45質量%以下,進而較佳為40質量%以下,進而較佳為35質量%以下。 進而,本發明之毛髮化妝料中之成分(B)與成分(C)之質量比(B)/(C)為0.8以上且99以下。於該範圍內時,本發明之毛髮化妝料其表面張力變得非常高,因此若應用於毛髮,則該液滴不僅橫向擴展且自發地於毛髮表面自上至下移動。推測結果毛髮化妝料中所含之聚合物自發且快速地於毛髮表面潤濕擴展,並且毛髮化妝料於毛髮表面快速乾燥。因此,塗抹後不易形成毛束,毛髮化妝料之存在感迅速消失,手感毫不黏膩,且賦予自然之整齊度。進而,於塗抹時無打滑感或黏糊感,亦無毛髮潮濕之觸感。就進一步提高該效果之觀點而言,成分(B)與成分(C)之質量比(B)/(C)較佳為1以上,更佳為1.2以上,進而較佳為1.5以上,進而較佳為2以上,且較佳為50以下,更佳為30以下,進而較佳為10以下,進而較佳為5以下。 又,關於本發明之毛髮化妝料中之成分(B)與成分(C)之合計含量,就乾燥後之輕盈感、劑無存在感之觀點而言為30質量%以上,較佳為50質量%以上,較佳為70質量%以上。又,較佳為99.9質量%以下,更佳為99質量%以下,進而較佳為98質量%以下。 [成分(D):穩定化劑] 本發明之毛髮化妝料就即便於高溫下保存亦不會出現分離而可穩定地保存之觀點而言,較佳為進而含有選自多元醇、脲、有機酸、聚氧伸烷基烷基葡糖苷及聚氧伸烷基甘油醚中之1種或2種以上作為成分(D)。作為較佳之多元醇,可列舉:1,3-丁二醇、甘油、聚甘油等。又,作為較佳之有機酸,可列舉:乳酸、蘋果酸、檸檬酸等。又,作為較佳之聚氧伸烷基烷基葡糖苷,可列舉:PPG-10甲基葡萄糖、PPG-20甲基葡萄糖、甲基葡萄糖10環氧乙烷、甲基葡萄糖20環氧乙烷等。又,作為較佳之聚氧伸烷基甘油醚,可列舉PEG/PPG/聚丁二醇-8/5/3甘油等。其中,就高溫保存穩定性之觀點而言,較佳為脲、乳酸、甘油,更佳為脲。 關於本發明之毛髮化妝料中之成分(D)之含量,就確保高溫穩定性之觀點而言,較佳為0.1質量%以上,更佳為0.5質量%以上,又,就確保自然之觸感之觀點而言,較佳為3質量%以下,更佳為2質量%以下。 [水] 本發明之毛髮化妝料較佳為不含水。其中,有時亦會不可避免地混入微量~少量(例如0.0001質量%以上)之水,於此種情形時,水分量亦較佳為較少。具體而言,水分之含量較佳為未達5質量%,更佳為未達3質量%,進而較佳為未達0.5質量%。 [任意成分] 本發明之毛髮化妝料中除了以上所說明之成分以外,亦可於無損本發明之效果之限度內含有成分(A)及(C)以外之化妝料用油劑。毛髮化妝料中之成分(A)及(C)以外之化妝料用油劑之含量較佳為0.1~10質量%。作為此種化妝料用油劑,可列舉:蓖麻油、可可油、貂油、萼梨油、橄欖油等甘油酯類;蜂蠟、鯨蠟、羊毛脂、巴西棕櫚蠟等蠟類;肉豆蔻酸異丙酯、月桂酸己酯、乳酸鯨蠟酯、單硬脂酸丙二醇酯、油酸油酯、2-乙基己酸十六烷基酯、肉豆蔻酸辛基十二烷基酸之酯類;二甲基聚矽氧烷、甲基苯基聚矽氧烷、環氧改性矽酮油、胺基改性矽酮油、烷基改性矽酮油等除成分(A)或(C)所含者以外之矽酮衍生物等。 進而,本發明之毛髮化妝料可含有用以提高商品價值之香料或色素、用以防止毛髮化妝料隨時間經過而變質之防腐劑或抗氧化劑,又,進而亦可視需要含有界面活性劑、硬化劑、抗靜電劑、消泡劑、分散劑、增黏劑、紫外線吸收劑、抗氧化劑、防腐劑、有色染料、染料定著劑、噴射劑等。 [劑型] 作為本發明之毛髮化妝料之劑型,並無特別限制,可為透明液狀、乳狀、乳液狀、霧狀(髮妝水噴霧、造型噴霧)、泡狀(慕絲)等,其中,較佳為製成以霧狀形態塗抹之劑型,更佳為非氣溶膠型之劑型。再者,於非氣溶膠型之劑型之情形時,就於成分(B)與成分(C)兩者中之分散性或溶解性優異之觀點而言,成分(A)較佳為兩親媒性被膜形成性高分子或聚醚改性矽酮。 再者,於將本發明之毛髮化妝料以包含氣溶膠原液與噴射劑之氣溶膠式毛髮化妝料之形式使用之情形時,各成分之含量係指不含噴射劑之氣溶膠原液之整體組成中之含量。 [整髮方法] 本發明之毛髮化妝料可較佳地用作整髮劑。關於作為整髮劑之使用方法、即整髮方法,只要為對毛髮應用本發明之毛髮化妝料而整理髮型之方法,則亦可採用任意方法。本發明之毛髮化妝料可應用於濕潤毛髮,亦可應用於乾燥毛髮,較佳為應用於乾燥毛髮。 例如較佳為直接呈霧狀地塗抹毛髮化妝料,一面用手梳理或使用髮梳、刷子等梳理一面整理毛髮形狀。 [實施例] 以下,藉由實施例而更具體地說明本發明。本發明並不限定於該等實施例。 [實施例1~6及比較例1~5] 藉由常規方法製備表1記載之毛髮化妝料,並依據下述方法及基準評價高溫穩定性及濕潤擴展性。 「高溫穩定性評價」 於50 mL玻璃瓶(廣口規格瓶 PS-N0.6;三商股份有限公司)內填裝表1之毛髮化妝料40 mL,蓋上蓋子加以密封。將其於50℃之恆溫槽中靜置2小時。其後自恆溫槽中取出,目視觀察玻璃瓶中之毛髮化妝料之形態。評價係基於下述基準進行。 A:未分離 B:產生白濁,但若恢復至室溫則復原為均勻溶液 C:即便恢復至室溫且進行振盪亦無法復原為均勻溶液 「濕潤擴展性評價」 作為毛髮之乾燥狀態之模型,使用表面為疏水性之200×200×3 mm之玻璃板(吸附劑塗佈用玻璃板100-2a,AS ONE股份有限公司製造)。將玻璃板以傾斜5°(左右為水平)之方式設置。使用微量吸管(Research Plus V 3120,Eppendorf公司製造)自高度5 mm處將表1記載之各毛髮化妝料50 μL滴至上述玻璃板上,經過1分鐘後測定於此期間液體移動之距離。 又,將表1記載之毛髮化妝料填充於吉野製作所公司製造之泵壓噴霧容器(使用使實施例、比較例之毛髮化妝料於呈霧狀噴出時之平均粒徑成為60 μm的噴霧器)內,依據以下之方法及基準進行性能評價。再者,比較例4由於組合物之黏度較高,無法以使用噴霧器呈霧狀噴灑之方式進行塗抹,故而於依據以下之方法及基準進行性能評價時採用將液劑取至手上後塗抹於毛束之方法。 (評價用毛束) 使用未曾經過化學處理之日本人之脆弱之不規則毛製作長30 cm、重8 g之毛束。對毛束塗抹3 g花王公司製造之SUCCESS藥用洗髮精h,起泡30秒後洗淨,利用40℃之自來水沖洗30秒。重複進行該洗髮精操作2次。繼而,塗抹3 g下述配方所示之樣品潤絲精,浸潤15秒後,利用40℃之自來水沖洗30秒。繼而,用毛巾擦乾後,使之於實驗室條件下自然乾燥6小時,將所獲得者用作評價用毛束。 (樣品潤絲精之組成)成分 ( 質量 %)
鯨蠟硬脂醇 2.0 氯化硬脂基三甲基銨 0.76 氯化二硬脂基二甲基銨 2.7 丙二醇 5.0 異丙醇 0.6 對羥基苯甲酸乙酯 0.1離子交換水 餘量
合計 100 (評價方法) 「剛塗抹後不久之乾燥速度」 對評價用毛束整體噴灑0.2 g填充於泵壓噴霧器內之各毛髮化妝料。噴灑後,用手梳理評價用毛束30次。基於下述基準,評價用手梳理期間之乾燥速度。 評價係由7名官能檢查員,針對於藉由上述操作使用各組合物進行處理時為「乾燥較快」/「難以評價」/「乾燥較慢」中之哪一項進行擇一性選擇。依序顯示回答乾燥較快/難以評價/乾燥較慢之官能檢查員之人數。 「剛塗抹後不久之乾澀感之有無」 藉由與「剛塗抹後不久之乾燥速度」相同之方法進行處理,針對用手反覆梳理1~10次期間有無乾澀感,基於下述基準進行評價。 評價係由7名官能檢查員,針對於藉由上述操作使用各組合物進行處理時為「無乾澀感」/「難以評價」/「有乾澀感」中之哪一項進行擇一性選擇。依序顯示回答無乾澀感/難以評價/有乾澀感之官能檢查員之人數。 「剛塗抹後不久之梳理性之良莠」 藉由與「剛塗抹後不久之乾燥速度」相同之方法進行處理,針對用手反覆梳理1~10次期間梳理性是否良好,基於下述基準進行評價。 評價係由7名官能檢查員,針對於藉由上述操作使用各組合物進行處理時為「梳理性良好」/「難以評價」/「梳理性較差」中之哪一項進行擇一性選擇。依序顯示回答梳理性良好/難以評價/梳理性較差之官能檢查員之人數。 「用手梳理時之黏膩感之有無」 藉由與「剛塗抹後不久之乾燥速度」相同之方法進行處理,針對用手梳理期間有無黏膩感,基於下述基準進行評價。 評價係由7名官能檢查員,針對於藉由上述操作使用各組合物進行處理時為「無黏膩感」/「難以評價」/「有黏膩感」中之哪一項進行擇一性選擇。依序顯示回答梳理性良好/難以評價/梳理性較差之官能檢查員之人數。 「乾燥後之毛束感之有無」 藉由與「剛塗抹後不久之乾燥速度」相同之方法進行處理,用手梳理結束後,放置3分鐘。其後,針對有無毛束感,基於下述基準進行評價。 評價係由7名官能檢查員,針對於藉由上述操作使用各組合物進行處理時為「無毛束感」/「稍有毛束感」/「有毛束感」中之哪一項進行擇一性選擇。依序顯示回答無毛束感/稍有毛束感/有毛束感之官能檢查員之人數。 「乾燥後之整齊度」 藉由與「剛塗抹後不久之乾燥速度」相同之方法進行處理,用手梳理結束後,放置3分鐘。其後,針對整齊度,基於下述基準進行評價。 評價係由7名官能檢查員,針對於藉由上述操作使用各組合物進行處理時為「整齊」/「稍整齊」/「不整齊」中之哪一項進行擇一性選擇。依序顯示回答整齊/稍整齊/不整齊之官能檢查員之人數。 「乾燥後之整髮劑之存在感之有無」 藉由與「剛塗抹後不久之乾燥速度」相同之方法進行處理,用手梳理結束後,放置3分鐘。其後,針對評價用毛束上之整髮劑、尤其聚合物有無存在感,基於下述基準進行評價。 評價係由7名官能檢查員,針對於藉由上述操作使用各組合物進行處理時為「無存在感」/「難以評價」/「有存在感」中之哪一項進行擇一性選擇。依序顯示回答無存在感/難以評價/有存在感之官能檢查員之人數。 「乾燥後之梳理性之良莠」 藉由與「剛塗抹後不久之乾燥速度」相同之方法進行處理,用手梳理結束後,放置3分鐘。其後,針對評價用毛束之梳理性,基於下述基準進行評價。 評價係由7名官能檢查員,針對於藉由上述操作使用各組合物進行處理時為「梳理性良好」/「難以評價」/「梳理性較差」中之哪一項進行擇一性選擇。依序顯示回答梳理性良好/難以評價/梳理性較差之官能檢查員之人數。 「乾燥後之強韌感」 藉由與「剛塗抹後不久之乾燥速度」相同之方法進行處理,用手梳理結束後,放置3分鐘。其後,針對評價用毛束之梳理性,基於下述基準進行評價。 評價係由7名官能檢查員,針對於藉由上述操作使用各組合物進行處理時為「有強韌感」/「難以評價」/「無強韌感」中之哪一項進行擇一性選擇。依序顯示回答有強韌感/難以評價/無強韌感之官能檢查員之人數。 [表1] When the hair oil of Patent Document 1 is applied to the wet hair after shampooing, it can impart a tidy feeling or a conditioning effect after drying, but when applied to dry hair, uneven application is still caused, so that after drying The problem of insufficient uniformity or poor touch. Further, if a sufficient amount is applied to uniformly coat the entire hair, there is also a problem that the hair feels heavy or the hair bundle feels after drying. Further, it is considered that the bifurcated hair styling agent of Patent Document 2 preferably contains 10 to 50% by weight, particularly 20 to 40% by weight, of the dimethyl polyoxane derivative in the entire composition in order to coat the bifurcated hair. Therefore, after drying, a large amount of the dimethyl polysiloxane derivative remaining on the hair causes the hair to feel heavy or hairy, and it is difficult to obtain a dry touch. Accordingly, the present invention relates to a hair cosmetic which has good wet spreadability when applied to dry hair and which dries immediately after application without causing dryness or moist feeling of the hair, and does not form a tuft after drying. The hair can be kept in a natural uniformity. The inventors of the present invention considered that the problem of the above nonaqueous hair cosmetic is mainly due to insufficient wet spreadability on dry hair and time consuming for volatilization of volatile oil after application. As a result, it has been found that when a specific ketone oil and a lower alcohol are set to a specific ratio, the surface tension of the solvent is remarkably increased, and the hair cosmetic applied to the hair spontaneously moves on the surface of the hair, and at the same time, the polymerization is contained. The object covers the surface of the hair. Further, it has been found that the polymer component contained can be quickly and evenly applied to the surface of the hair, thereby drying extremely quickly, so that the feeling of the hair cosmetic on the hair disappears shortly after application, and the hair after drying is kept neat. , thus completing the invention. The hair cosmetic of the present invention spontaneously moves on the surface of the hair of dry hair and dries quickly. Therefore, the polymer in the hair cosmetic material spreads quickly and evenly on the surface of the hair, and the feeling of the hair cosmetic material disappears rapidly after application, and there is no unnatural hairiness, the hand feel is not sticky, and the natural tidyness is imparted. degree. Further, there is no dry feeling or sticky feeling when applied, and there is no wet feeling of hair. [Component (A): Polymer for hair cosmetic having solubility or dispersibility in water or ethanol] Component (A) is a polymer which is dissolved or stably dispersed in water or ethanol even without using a surfactant. And it can be stably present in a component such as the component (B) having a polar solvent. This component (A) is a component which is uniformly applied to the surface of the hair by the constitution of the present invention, thereby imparting a natural sense of neatness or a natural touch to the hair without feeling the presence of the polymer. As such a polymer for hair cosmetic which has solubility or dispersibility in water or ethanol, a film-forming polymer or a polyether-modified anthrone is preferable. From the viewpoint of further enhancing the feeling of uniformity, it is preferred to use a film-forming polymer as the component (A). The film-forming polymer which can be used as the component (A) is not particularly limited as long as it has solubility or dispersibility in water or ethanol, and can be used in a case where the fixing force is generally higher for the hair styling agent. Any of the relatively low setting forces. Examples of such a film-forming polymer include an anthrone-based graft polymer, an urethane-based polymer compound, a polyvinylpyrrolidone-based polymer compound, an anionic vinyl ether-based polymer compound, and an anion. Polyvinyl acetate polymer compound, anionic (meth)acrylic polymer compound, amphoteric (meth)acrylic polymer compound, nonionic (meth)acrylic polymer compound, cationic (A An acrylic polymer compound or a maleimide polymer compound. Examples of the anthrone-based graft polymer include poly(N-methyl decylethylidene) organopolyoxyalkylene, poly(N-ethyl fluorenylethylenimine) organopolyoxy siloxane, and poly( N-propionyl extended ethyl imine) polyoxafluorone-9 such as organopolyoxyalkylene; organopolyoxyalkylene graft polymer described in International Publication No. 2014/002707; KP-545 (Shin-Etsu Chemical Industry Co., Ltd.) and other alkyl acrylate copolymers such as methyl polyoxyalkylene ester; Silsoft Spread TT (Momentive) and other polyketone-17; Luviflex Silk (BASF) and other alkyl acrylates and methacrylic acid・Anthrone copolymers, etc. Among these, in terms of stereotype, no stickiness when dry, softness after application, and combability after application, it is more preferable to be a poly(N-methylstilbeneethylenimine) organic polyfluorene. Polyoxanone, poly(N-ethyl fluorenylethylenimine), organopolyoxyalkylene, poly(N-propionylethylidene), organopolyoxyalkylene, polyketone-9, polyfluorenone-28 An alkyl polyoxyalkylene acrylate copolymer such as an organopolyoxane graft polymer described in International Publication No. 2014/002707 or KP-545 (Shin-Etsu Chemical Co., Ltd.). Examples of the urethane-based polymer compound include polyurethanes such as Luviset PUR (BASF Japan) and polyurethane-14 AMP-acrylate copolymers such as DynamX (AkzoNobel Co., Ltd.). . Examples of the polyvinylpyrrolidone-based polymer compound include Luviskol K12, Luviskol K17, Luviskol K30, Luviskol L60, Luviskol K80, Luviskol K90 (BASF); PVP K15, PVP K17, PVP K30, PVP K60, PVP. Polyvinylpyrrolidone such as K90, PVP K120 (above Ashland); Luviskol VA28, Luviskol VA37, Luviskol VA55, Luviskol VA64P, Luviskol VA73 (above BASF); Luviskol Plus (BASF) and other polyethylene Indoleamine; PVP/VA E-735, PVP/VA E-635, PVP/VA E-535, PVP/VA E-335, PVP/VA S-630, PVP/VA W-735 (above is Ashland (Vinyl pyrrolidone/vinyl acetate) copolymer; polyvinylpyrrolidone/vinyl acetate/vinyl propionate terpolymer such as Luviskol VAP343 (BASF); Luviflex (BASF); Copolymer 845, Copolymer 937, Copolymer 958 (above Ashland) and other polyvinylpyrrolidone / dimethylaminomethyl / acrylic copolymer; Copolymer VC-713 (Ashland) and other polyvinylpyrrolidone / A Dimethylaminoethyl acrylate/vinyl caprolactam copolymer; Lu Viset Clear (BASF) and other (VP/methacrylamide/vinylimidazole) copolymer; Luviquat HM552 (BASF) and other vinyl imidazolium methyl chloride/vinyl pyrrolidone copolymer. Among these, it is more preferably (vinylpyrrolidone/vinyl acetate) copolymerization from the viewpoint of smoothness, setting property, no stickiness when dry, and softness after application just after application. , polyvinylpyrrolidone. Examples of the anionic vinyl ether-based polymer compound include a (vinyl vinyl ether/maleic acid ethyl ester) copolymer such as Gantrez ES-225 (Ashland Corporation), and Gantrez ES-425 (Ashland Corporation) (ethylene). Methyl ether / butyl maleate copolymer, and the like. Among these, a (vinyl methyl ether/butyl methacrylate) copolymer is preferred from the viewpoints of stereotype, no stickiness upon drying, and softness after application. Examples of the anionic polyvinyl acetate-based polymer compound include vinyl acetate/butenoic acid copolymers such as Resin 28-1310 (AkzoNobel Co., Ltd.) and Luviset CA66 (BASF Co., Ltd.); and Resin 28-2930 (Akzo Nobel Co., Ltd.). (vinyl acetate/crotonic acid/vinyl neodecanoate) copolymer; vinyl acetate/butenoic acid/vinyl propionate copolymer such as Luviset CAP (BASF). Examples of the anionic (meth)acrylic polymer compound include acrylic resin alkanolamine liquids such as Plas-size L-53P and Plas-size L-9540B (above, Mutual Chemical Industry Co., Ltd.); Diahold (Mitsubishi) Acrylic acid/acrylic acid ester copolymer; such as acrylic acid/acrylate copolymer; Ultrahold 8, Ultrahold strong (above BASF), or AMPHOMER V-42, DEMACRYL 79 (above AkzoNobel); Aniset NF-1000, Aniset HS-3000 (above, Osaka Organic Chemical Industry Co., Ltd.) and other alkyl acrylate copolymers. Examples of the amphoteric (meth)acrylic polymer compound include Yukaformer M-75, Yukaformer R205, Yukaformer 301, Yukaformer SM (above, Mitsubishi Chemical Corporation), and RAM Resin (Osaka Organic Chemical Co., Ltd.). Oxyethylcarboxybetaine/alkyl methacrylate copolymer; AMPHOMER 28-4910, AMPHOMER LV-71 (above AkzoNobel), etc. (octyl acrylamide/hydroxypropyl acrylate/methacrylic acid butyl Aminoethyl ester) copolymer; AMPHOMER HC (AkzoNobel), etc. (alkyl acrylate/octyl acrylamide) copolymer; DIAFORMER Z-651 (Mitsubishi Chemical Co., Ltd.), etc. (acrylate/lauryl acrylate/ Stearic acid acrylate / ethyl oxyalkyl methacrylate copolymer, and the like. Among these, in terms of stereotype, no stickiness upon drying, and softness after application, (methacryloxyethyl carboxybetaine/alkyl methacrylate) copolymerization is preferred. Things. Examples of the nonionic (meth)acrylic polymer compound include Plas-size L-2700 and Plas-size L-2714 (above, Mutual Chemical Industry Co., Ltd.) (dimethacrylamide/acrylic acid hydroxyl group). Ethyl ester / methoxyethyl acrylate copolymer and the like. Examples of the cationic (meth)acrylic polymer compound include an alkyl acrylamide/acrylate/alkylaminoalkyl acrylamide/polyethylene glycol described in JP-A-2-180911. A methacrylate copolymer; an alkyl acrylamide/alkylaminoalkyl acrylamide/polyethylene glycol methacrylate copolymer described in Japanese Patent Laid-Open No. Hei 8-291206; Plas-size L- 515 (Mujia Chemical Industry Co., Ltd.) and other poly-quaternary ammonium salt-99; Aquaflex SF-40 (Ashland) and other (PVP / vinyl caprolactam / acrylic acid DMAPA) copolymer; STYLEZE CC-10 (Ashland) (vinylpyrrolidone/acrylic acid DMAPA) copolymer; Luviquat PQ11 (BASF), GAFQUAT 734, GAFQUAT 755 (above Ashland) vinylpyrrolidone/dimethylamino methacrylate copolymer The quaternary compound (poly quaternary ammonium salt-11). Among them, an alkyl acrylamide/acrylate/alkylaminoalkyl acrylamide/polyethylene glycol methacrylate copolymer described in Japanese Laid-Open Patent Publication No. Hei No. 2-180911, Japanese Patent Laid-Open An alkyl acrylamide/alkylaminoalkyl decylamine/polyethylene glycol methacrylate copolymer or a polytetra-ammonium salt-11 described in 8-291206. Examples of the maleimide-based polymer compound include copolymerization of isobutylene/ethyl maleimide/hydroxyethyl maleimide, such as Aquaflex FX-64 (ISP Japan). Things. Among these film-forming polymers, an anthrone-based graft polymer or a polyvinylpyrrolidone-based polymer is preferable in terms of setting property, no stickiness during drying, and softness after application. A compound, an anionic polyvinyl acetate-based polymer compound, an amphoteric (meth)acrylic polymer compound, a nonionic (meth)acrylic polymer, and a cationic (meth)acrylic compound. On the other hand, from the viewpoint of having no dry feeling immediately after application and further improving the uniformity after drying, it is preferred to use a polyether-modified anthrone as the component (A). The polyether-modified fluorenone which can be used as the component (A) is not particularly limited as long as it has solubility or dispersibility in water or ethanol, and examples thereof include polyoxyethylene modified fluorenone and polypropylene. The fluorenone, the polyoxyethylene/polyoxypropylene-modified fluorenone, the polyglycerin-modified fluorenone, and the like, and the modified form may, for example, be a side chain type (side chain modified type) or a linear copolymer type. As such a polyether-modified anthrone, a copolymer having a block chain of an organic siloxane chain and a polyalkyl chain is preferable, and examples thereof include Silsoft A+ (Momentive) and the like (PEG-40/PPG- 8 methylaminopropyl/hydroxypropyl dimethyl polyoxyalkylene) copolymer; polyfluorenone-13 such as FZ-2222, FZ-2233, CB2250 (Dow Corning Toray); Silwet L-8600 (Momentive) PEG-12 dimethoxane, such as PEG-12 dimethyl polyoxy siloxane, Silsoft 900 (Momentive), PEG-10 dimethyl polyoxy siloxane such as Silsoft 860 (Momentive); SILSTYLE 104 (Dow) Corning Toray Co., Ltd. (bisisobutyl PEG-14/amino dimethylpolyoxane) copolymer; SILSTYLE 401 (Dow Corning Toray), etc. (bisisobutyl PEG/PPG-20/35/amino group Dimethicone Copolymer; CE-8411 Smooth Plus Emulsion (Dow Corning Toray), etc. Bis-isopropanolamine-PG-propyldimethylpolyoxane/bisisobutyl PEG-14 copolymer A product such as DOW CORNING TORAY SS-3588 (Dow Corning Toray Co., Ltd.) or the like (bisisobutyl PEG-15/aminodimethylpolysiloxane) copolymer. Among them, a copolymer having an amine-modified organopolyoxyalkylene chain and a block chain of a polyoxyalkylene chain is preferred, and more preferably (bisisobutyl PEG-14/amino dimethylpolyoxyl) Copolymer, (bisisobutyl PEG/PPG-20/35/amino dimethylpolyoxyalkylene) copolymer, bis-isopropanolamine-PG-propyl dimethylpolyoxane/double A linear copolymerized amino group/polyether modified anthrone such as an isobutyl PEG-14 copolymer or a (bisisobutyl PEG-15/aminodimethylpolysiloxane) copolymer, and further preferably It is a (bisisobutyl PEG-15/aminodimethylpolyoxane) copolymer. The polymer for hair cosmetic materials may be used singly or in combination of two or more kinds, and it is preferred to form the polymer into the film from the viewpoint of further improving the natural sensation and the natural touch. It is used together with the polyether modified anthrone as the component (A). Further, the component (A) is preferably an amphiphilic film forming property from the viewpoint of imparting a sticky feeling during drying, leaving it thin and evenly on the hair, and further imparting a natural touch and uniformity. Polymer or polyether modified anthrone. The amphiphilic film-forming polymer is a styling polymer containing 10 to 98% of a hydrophobic portion in terms of a mass ratio. Examples of such an amphiphilic styling polymer include polyfluorenone-9 and polyfluorene. Keto-28, especially preferably polyketone-9. The content of the component (A) in the hair cosmetic of the present invention is 0.1% by mass or more, preferably 0.5% by mass or more, and more preferably 1% by mass or more from the viewpoint of imparting uniformity to the hair. In addition, it is 10 mass% or less, preferably 7% by mass or less, and more preferably 5% by mass, from the viewpoint of feeling that the hair feels heavy or does not cause a hairiness, and gives a natural touch and a sense of uniformity. the following. [Component (B): One-to-one carbon of 1 to 4 carbons] The component (B) is controlled by combining with the component (C) to control the wet spreadability of the hair cosmetic containing the component (A) and the drying on the hair. The composition of speed. As the monohydric alcohol having 1 to 4 carbon atoms of the component (B), a saturated or unsaturated aliphatic alcohol can be used. These monohydric alcohols may be used alone or in combination of two or more. The alcohol is preferably ethanol, propanol, isopropanol or tert-butanol, more preferably ethanol or isopropanol, and still more preferably ethanol. The content of the component (B) in the hair cosmetic of the present invention is preferably 45 mass% or more, more preferably 55 mass% or more, and still more preferably 60 mass, from the viewpoint of drying speed and beamlessness. In addition, it is preferably 98% by mass or less, more preferably 90% by mass or less, still more preferably 80% by mass or less, and still more preferably 75% by mass or less from the viewpoint of having no dry feeling after application. [Component (C): Anthrone having a number average molecular weight of 100 or more and 1,500 or less] The component (C) is an anthrone having a number average molecular weight of 100 or more and 1,500 or less, and is controlled by combining with the component (B). A component of the moist spreadability of a cosmetic and the drying speed of the hair cosmetic on the hair. Examples of such an anthrone include cyclic ketones such as octamethylcyclotetraoxane, decamethylcyclopentaoxane, dodecamethylcyclohexaoxane, and methylcyclopolyoxyalkylene. ; octamethyltrioxane, tetradecyl hexaoxane, methyltrimethylpolyoxyalkylene, a dynamic viscosity at 25 ° C, for example, a methyl group of 0.5 mm 2 /s or more and 10 mm 2 /s or less Chain fluorenone such as polyoxyalkylene. Among them, preferred are decamethylcyclopentaoxane, methyltrimethylpolyoxyalkylene, methyl polyoxyalkylene having an kinetic viscosity at 25 ° C of 0.5 mm 2 /s or more and less than 6 mm 2 /s. The iso-chain fluorenone is more preferably decamethylcyclopentaoxane or methyltrimethylpolyoxyalkylene. The number average molecular weight of the component (C) is preferably 100 or more, more preferably 150 or more, and still more preferably 200 or more from the viewpoint of good smoothness after application and combability. Further, from the viewpoint of no hairiness after drying and feeling light, it is preferably 1,000 or less, more preferably 700 or less, still more preferably 500 or less. Further, the component (C) is preferably a volatile fluorenone from the viewpoint of lightness after drying or a feeling of no presence of the agent. The volatile fluorenone is a high volatile organic compound, a volatile organic compound defined by WHO (World Health Organization), and an anthrone having a boiling point of 260 ° C or lower. Further, as the volatile fluorenone, those having a boiling point of 50 ° C or higher are preferred. The content of the component (C) in the hair cosmetic of the present invention is preferably 1% by mass or more, more preferably 10% by mass or more, from the viewpoint of good smoothness and combability after application. It is preferably 20% by mass or more, more preferably 25% by mass or more, and is preferably 52% by mass or less, more preferably 45% by mass or less, from the viewpoint of a hairless feeling after drying and feeling light. It is preferably 40% by mass or less, and more preferably 35% by mass or less. Further, the mass ratio (B)/(C) of the component (B) to the component (C) in the hair cosmetic of the present invention is 0.8 or more and 99 or less. Within this range, the hair cosmetic of the present invention has a very high surface tension, so that if applied to the hair, the droplet not only spreads laterally but spontaneously moves from top to bottom on the surface of the hair. It is speculated that the polymer contained in the hair cosmetic material spontaneously and rapidly wets and spreads on the surface of the hair, and the hair cosmetic material is rapidly dried on the surface of the hair. Therefore, it is difficult to form a hair bundle after application, and the presence of the hair cosmetic material quickly disappears, the hand feel is not sticky, and the natural uniformity is imparted. Further, there is no slippery feeling or sticky feeling when applied, and there is no wet feeling of hair. From the viewpoint of further improving the effect, the mass ratio (B)/(C) of the component (B) to the component (C) is preferably 1 or more, more preferably 1.2 or more, still more preferably 1.5 or more, and further preferably It is preferably 2 or more, and is preferably 50 or less, more preferably 30 or less, still more preferably 10 or less, still more preferably 5 or less. In addition, the total content of the component (B) and the component (C) in the hair cosmetic of the present invention is 30% by mass or more, preferably 50%, from the viewpoint of the lightness after drying and the presence of the agent. % or more, preferably 70% by mass or more. Further, it is preferably 99.9% by mass or less, more preferably 99% by mass or less, and still more preferably 98% by mass or less. [Component (D): Stabilizer] The hair cosmetic of the present invention preferably contains a selected from the group consisting of a polyol, a urea, and an organic substance, even if it is stored at a high temperature without separation and can be stably stored. One or two or more kinds of the acid, the polyoxyalkylene alkyl glucoside, and the polyoxyalkylene glyceryl ether are used as the component (D). Preferred examples of the polyhydric alcohol include 1,3-butylene glycol, glycerin, and polyglycerin. Moreover, as a preferable organic acid, lactic acid, malic acid, citric acid, etc. are mentioned. Further, preferred examples of the polyoxyalkylalkyl glucoside include PPG-10 methyl glucose, PPG-20 methyl glucose, methyl glucose 10 ethylene oxide, methyl glucose 20 ethylene oxide, and the like. . Further, preferred examples of the polyoxyalkylene glycol glyceryl ether include PEG/PPG/polybutylene glycol-8/5/3 glycerin. Among them, from the viewpoint of high-temperature storage stability, urea, lactic acid, glycerin, and more preferably urea are preferred. The content of the component (D) in the hair cosmetic of the present invention is preferably 0.1% by mass or more, more preferably 0.5% by mass or more, from the viewpoint of ensuring high-temperature stability, and ensures a natural touch. From the viewpoint of the above, it is preferably 3% by mass or less, and more preferably 2% by mass or less. [Water] The hair cosmetic of the present invention preferably does not contain water. Among them, a small amount to a small amount (for example, 0.0001% by mass or more) of water may be inevitably mixed, and in this case, the amount of water is preferably less. Specifically, the content of moisture is preferably less than 5% by mass, more preferably less than 3% by mass, still more preferably less than 0.5% by mass. [Optional component] In addition to the components described above, the hair cosmetic of the present invention may contain an oil for cosmetics other than the components (A) and (C) within the limits of the effects of the present invention. The content of the oil agent for cosmetics other than the components (A) and (C) in the hair cosmetic is preferably from 0.1 to 10% by mass. Examples of the oil agent for such a cosmetic include glycerides such as castor oil, cocoa butter, eucalyptus oil, avocado oil, and olive oil; waxes such as beeswax, cetyl wax, lanolin, and carnauba wax; and myristic acid. Isopropyl ester, hexyl laurate, cetyl lactate, propylene glycol monostearate, oleic acid oil ester, cetyl 2-ethylhexanoate, ester of octyl dodecyl acid myristate ; dimethyl polysiloxane, methyl phenyl polyoxy siloxane, epoxy modified fluorenone oil, amine modified fluorenone oil, alkyl modified fluorenone oil, etc. In addition to the component (A) or (C ) an anthrone derivative other than those contained in the product. Further, the hair cosmetic of the present invention may contain a perfume or a pigment for enhancing the commercial value, a preservative or an antioxidant for preventing deterioration of the hair cosmetic over time, and further, may optionally contain a surfactant and harden. Agents, antistatic agents, defoamers, dispersants, tackifiers, UV absorbers, antioxidants, preservatives, colored dyes, dye fixatives, propellants, etc. [Formulation] The dosage form of the hair cosmetic of the present invention is not particularly limited, and may be a transparent liquid, a milky, an emulsion, a mist (a makeup spray, a styling spray), a foam (mousse), or the like. Among them, a dosage form to be applied in a mist form is preferred, and a non-aerosol type dosage form is more preferred. Further, in the case of a non-aerosol type, the component (A) is preferably an amphiphilic agent from the viewpoint of excellent dispersibility or solubility in both the component (B) and the component (C). A film-forming polymer or a polyether-modified anthrone. Furthermore, in the case where the hair cosmetic of the present invention is used in the form of an aerosol hair cosmetic containing an aerosol stock solution and a propellant, the content of each component means the overall composition of the aerosol stock solution containing no propellant. The content in the middle. [Whole Hair Method] The hair cosmetic of the present invention can be preferably used as a hair styling agent. As a method of using the hair styling agent, that is, the hair styling method, any method may be employed as long as the hair styling method of the present invention is applied to the hair and the hair styling method is used. The hair cosmetic of the present invention can be applied to wet hair, and can also be applied to dry hair, preferably to dry hair. For example, it is preferred to apply the hair cosmetic directly in a mist form, and to comb the hair shape by combing with a comb or a brush. [Examples] Hereinafter, the present invention will be more specifically described by way of examples. The invention is not limited to the embodiments. [Examples 1 to 6 and Comparative Examples 1 to 5] The hair cosmetics described in Table 1 were prepared by a conventional method, and high-temperature stability and wettability were evaluated in accordance with the following methods and criteria. "High-Temperature Stability Evaluation" Fill 40 mL of the hair cosmetic of Table 1 in a 50 mL glass bottle (Guangkou size bottle PS-N0.6; Sanshang Co., Ltd.), and cover with a lid to seal. This was allowed to stand in a thermostat at 50 ° C for 2 hours. Thereafter, it was taken out from the constant temperature bath, and the form of the hair cosmetic in the glass bottle was visually observed. The evaluation was performed based on the following criteria. A: unseparated B: white turbidity is produced, but if it returns to room temperature, it is restored to a uniform solution C: even if it is returned to room temperature and shaken, it cannot be restored to a uniform solution "wet spreadability evaluation" as a model of dry state of hair. A glass plate (glass plate 100-2a for adsorbent coating, manufactured by AS ONE Co., Ltd.) having a hydrophobic surface of 200 × 200 × 3 mm was used. The glass plate was set at an inclination of 5° (horizontal left and right). 50 μL of each of the hair cosmetic materials described in Table 1 was dropped onto the glass plate from a height of 5 mm using a micropipette (Research Plus V 3120, manufactured by Eppendorf Co., Ltd.), and the distance of liquid movement during this period was measured after one minute. In addition, the hair cosmetic preparations of Table 1 were filled in a pump spray container manufactured by Yoshino Seisakusho Co., Ltd. (a sprayer having an average particle diameter of 60 μm when the hair cosmetics of the examples and the comparative examples were sprayed in a mist form) , performance evaluation based on the following methods and benchmarks. Furthermore, in Comparative Example 4, since the viscosity of the composition was high, it could not be sprayed by means of a sprayer, and the liquid was applied to the hand and applied to the performance evaluation according to the following methods and standards. The method of hair bundles. (Evaluation of hair bundles) A wool with a length of 30 cm and a weight of 8 g was produced using the fragile irregular hair of a Japanese who had not been chemically treated. Apply 3 g of medicinal shampoo h manufactured by Kao Co., Ltd. to the hair bundle, rinse for 30 seconds, and rinse with tap water at 40 °C for 30 seconds. This shampooing operation was repeated twice. Then, 3 g of the sample conditioner shown in the following formulation was applied, and after soaking for 15 seconds, it was rinsed with tap water of 40 ° C for 30 seconds. Then, after drying with a towel, it was naturally dried under laboratory conditions for 6 hours, and the obtained one was used as a hair bundle for evaluation. (Composition of sample rinse) Composition ( % by mass ) Cetearyl alcohol 2.0 Chlorostearyl trimethyl ammonium 0.76 Distearyl dimethyl ammonium chloride 2.7 Propylene glycol 5.0 Isopropyl alcohol 0.6 P-hydroxybenzoic acid Ethyl acetate 0.1 Ion exchange water balance Total 100 (Evaluation method) "Drying speed immediately after application" 0.2 g of each hair cosmetic filled in the pump sprayer was sprayed on the evaluation hair bundle. After spraying, the hair bundle for evaluation was combed by hand 30 times. The drying speed during the carding by hand was evaluated based on the following criteria. The evaluation was performed by seven functional inspectors for which one of "drying faster" / "difficult to evaluate" / "slow drying" was performed when the respective compositions were treated by the above operation. The number of functional inspectors who answered faster/difficult to evaluate/slower drying were displayed in sequence. "The presence or absence of dryness immediately after application" was treated by the same method as "drying speed immediately after application", and the feeling of dryness was repeated for 1 to 10 times by hand, and evaluated based on the following criteria. The evaluation was carried out by seven functional inspectors for which one of the "no dry feeling" / "difficult to evaluate" / "having a dry feeling" was selectively used when the respective compositions were treated by the above operation. The number of functional inspectors who answered no dry feelings/difficult to evaluate/having a sense of dryness were displayed in sequence. "The combing of the rationality just after the application" is handled by the same method as the "drying speed immediately after the application", and the combing is performed smoothly for 1 to 10 times by hand, based on the following criteria. Evaluation. The evaluation was carried out by seven functional inspectors for which one of the "comfortable good" / "difficult to evaluate" / "poor combability" was selected when the respective compositions were treated by the above operation. The number of functional inspectors with good combability/difficulty evaluation/comparable combing is displayed in sequence. "The presence or absence of the sticky feeling when combing by hand" was treated by the same method as "drying speed immediately after application", and the presence or absence of a sticky feeling during hand combing was evaluated based on the following criteria. The evaluation was conducted by seven functional inspectors for which one of the "non-sticky feeling" / "difficult to evaluate" / "sticky feeling" was used when the respective compositions were treated by the above operation. select. The number of functional inspectors with good combability/difficulty evaluation/comparable combing is displayed in sequence. "The presence or absence of the feeling of the hair after drying" was treated by the same method as "the drying speed immediately after the application", and the hand was finished for 3 minutes. Thereafter, the evaluation was carried out based on the following criteria with respect to the presence or absence of a hairiness. The evaluation was carried out by seven functional inspectors for which one of the "hairless beam feeling" / "slightly hairy feeling" / "hairy feeling" was used when the respective compositions were treated by the above operation. Alternative choice. The number of functional inspectors who answered the hairlessness/slightly hairy/hairy feeling was displayed in sequence. The "degree of uniformity after drying" was treated by the same method as "drying speed immediately after application", and after combing by hand, it was left for 3 minutes. Thereafter, the evaluation was performed based on the following criteria with respect to the uniformity. The evaluation was performed by seven functional inspectors for which one of "tidy"/"slightly neat"/"untidy" was used when processing each composition by the above operation. The number of functional inspectors who answered neatly/slightly neat/untidy was displayed in sequence. "The presence or absence of the feeling of the hair styling after drying" was treated by the same method as the "drying speed immediately after application", and after the carding was completed, it was left for 3 minutes. Thereafter, the presence or absence of a hair styling agent, particularly a polymer, on the evaluation hair bundle was evaluated based on the following criteria. The evaluation was performed by seven panelists in accordance with which of the "no sense of presence" / "difficult to evaluate" / "having a sense of presence" when using the respective compositions by the above operation. The number of functional inspectors who answered no sense of presence/difficult to evaluate/have a sense of presence was displayed in sequence. The "comfort of combing after drying" was treated by the same method as "drying speed immediately after application", and after combing by hand, it was left for 3 minutes. Thereafter, the combability of the evaluation hair bundle was evaluated based on the following criteria. The evaluation was carried out by seven functional inspectors for which one of the "comfortable good" / "difficult to evaluate" / "poor combability" was selected when the respective compositions were treated by the above operation. The number of functional inspectors with good combability/difficulty evaluation/comparable combing is displayed in sequence. The "toughness after drying" was treated by the same method as "drying speed immediately after application", and after finishing by hand, it was left for 3 minutes. Thereafter, the combability of the evaluation hair bundle was evaluated based on the following criteria. The evaluation was conducted by seven functional inspectors for which one of the "strongness", "difficult to evaluate", and "no-toughness" was used for the treatment with each composition by the above operation. select. The number of functional inspectors who responded with a strong/hard-to-evaluate/no-toughness was displayed in sequence. [Table 1]