JPWO2020166674A1 - 有機アンモニウム塩を含む組成物 - Google Patents
有機アンモニウム塩を含む組成物 Download PDFInfo
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- JPWO2020166674A1 JPWO2020166674A1 JP2020572316A JP2020572316A JPWO2020166674A1 JP WO2020166674 A1 JPWO2020166674 A1 JP WO2020166674A1 JP 2020572316 A JP2020572316 A JP 2020572316A JP 2020572316 A JP2020572316 A JP 2020572316A JP WO2020166674 A1 JPWO2020166674 A1 JP WO2020166674A1
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- 125000004432 carbon atom Chemical group C* 0.000 claims description 59
- 125000000217 alkyl group Chemical group 0.000 claims description 55
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- GGHPAKFFUZUEKL-UHFFFAOYSA-M sodium;hexadecyl sulfate Chemical compound [Na+].CCCCCCCCCCCCCCCCOS([O-])(=O)=O GGHPAKFFUZUEKL-UHFFFAOYSA-M 0.000 description 1
- UPUIQOIQVMNQAP-UHFFFAOYSA-M sodium;tetradecyl sulfate Chemical compound [Na+].CCCCCCCCCCCCCCOS([O-])(=O)=O UPUIQOIQVMNQAP-UHFFFAOYSA-M 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000001593 sorbitan monooleate Substances 0.000 description 1
- 235000011069 sorbitan monooleate Nutrition 0.000 description 1
- 229940035049 sorbitan monooleate Drugs 0.000 description 1
- 239000001587 sorbitan monostearate Substances 0.000 description 1
- 235000011076 sorbitan monostearate Nutrition 0.000 description 1
- 229940035048 sorbitan monostearate Drugs 0.000 description 1
- 235000012424 soybean oil Nutrition 0.000 description 1
- 239000003549 soybean oil Substances 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 229940012831 stearyl alcohol Drugs 0.000 description 1
- 150000003440 styrenes Chemical class 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-L succinate(2-) Chemical compound [O-]C(=O)CCC([O-])=O KDYFGRWQOYBRFD-UHFFFAOYSA-L 0.000 description 1
- 239000005720 sucrose Substances 0.000 description 1
- 150000003871 sulfonates Chemical class 0.000 description 1
- 125000000542 sulfonic acid group Chemical group 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 229910021653 sulphate ion Inorganic materials 0.000 description 1
- 210000004243 sweat Anatomy 0.000 description 1
- YIBXWXOYFGZLRU-UHFFFAOYSA-N syringic aldehyde Natural products CC12CCC(C3(CCC(=O)C(C)(C)C3CC=3)C)C=3C1(C)CCC2C1COC(C)(C)C(O)C(O)C1 YIBXWXOYFGZLRU-UHFFFAOYSA-N 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- 229940095064 tartrate Drugs 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- JRMUNVKIHCOMHV-UHFFFAOYSA-M tetrabutylammonium bromide Chemical compound [Br-].CCCC[N+](CCCC)(CCCC)CCCC JRMUNVKIHCOMHV-UHFFFAOYSA-M 0.000 description 1
- BFKJFAAPBSQJPD-UHFFFAOYSA-N tetrafluoroethene Chemical group FC(F)=C(F)F BFKJFAAPBSQJPD-UHFFFAOYSA-N 0.000 description 1
- OULAJFUGPPVRBK-UHFFFAOYSA-N tetratriacontyl alcohol Natural products CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCO OULAJFUGPPVRBK-UHFFFAOYSA-N 0.000 description 1
- 229940026510 theanine Drugs 0.000 description 1
- 229920005992 thermoplastic resin Polymers 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 125000002813 thiocarbonyl group Chemical group *C(*)=S 0.000 description 1
- 125000005300 thiocarboxy group Chemical group C(=S)(O)* 0.000 description 1
- 125000000101 thioether group Chemical group 0.000 description 1
- 125000003396 thiol group Chemical group [H]S* 0.000 description 1
- UMGDCJDMYOKAJW-UHFFFAOYSA-N thiourea group Chemical group NC(=S)N UMGDCJDMYOKAJW-UHFFFAOYSA-N 0.000 description 1
- UAXOELSVPTZZQG-UHFFFAOYSA-N tiglic acid Natural products CC(C)=C(C)C(O)=O UAXOELSVPTZZQG-UHFFFAOYSA-N 0.000 description 1
- FGMPLJWBKKVCDB-UHFFFAOYSA-N trans-L-hydroxy-proline Natural products ON1CCCC1C(O)=O FGMPLJWBKKVCDB-UHFFFAOYSA-N 0.000 description 1
- LDHQCZJRKDOVOX-UHFFFAOYSA-N trans-crotonic acid Natural products CC=CC(O)=O LDHQCZJRKDOVOX-UHFFFAOYSA-N 0.000 description 1
- QURCVMIEKCOAJU-UHFFFAOYSA-N trans-isoferulic acid Natural products COC1=CC=C(C=CC(O)=O)C=C1O QURCVMIEKCOAJU-UHFFFAOYSA-N 0.000 description 1
- UWHZIFQPPBDJPM-BQYQJAHWSA-N trans-vaccenic acid Chemical compound CCCCCC\C=C\CCCCCCCCCC(O)=O UWHZIFQPPBDJPM-BQYQJAHWSA-N 0.000 description 1
- 230000014616 translation Effects 0.000 description 1
- YNJBWRMUSHSURL-UHFFFAOYSA-N trichloroacetic acid Chemical compound OC(=O)C(Cl)(Cl)Cl YNJBWRMUSHSURL-UHFFFAOYSA-N 0.000 description 1
- KJLVNAWDXGBRAR-UHFFFAOYSA-N trimethyl-[methyl(silyloxysilyloxysilyloxysilyloxy)silyl]oxysilane Chemical compound C[SiH](O[Si](C)(C)C)O[SiH2]O[SiH2]O[SiH2]O[SiH3] KJLVNAWDXGBRAR-UHFFFAOYSA-N 0.000 description 1
- SMYKBXMWXCZOLU-UHFFFAOYSA-N tris-decyl benzene-1,2,4-tricarboxylate Chemical compound CCCCCCCCCCOC(=O)C1=CC=C(C(=O)OCCCCCCCCCC)C(C(=O)OCCCCCCCCCC)=C1 SMYKBXMWXCZOLU-UHFFFAOYSA-N 0.000 description 1
- 229960002703 undecylenic acid Drugs 0.000 description 1
- JOYRKODLDBILNP-UHFFFAOYSA-N urethane group Chemical group NC(=O)OCC JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
- 229940005605 valeric acid Drugs 0.000 description 1
- WKOLLVMJNQIZCI-UHFFFAOYSA-N vanillic acid Chemical compound COC1=CC(C(O)=O)=CC=C1O WKOLLVMJNQIZCI-UHFFFAOYSA-N 0.000 description 1
- TUUBOHWZSQXCSW-UHFFFAOYSA-N vanillic acid Natural products COC1=CC(O)=CC(C(O)=O)=C1 TUUBOHWZSQXCSW-UHFFFAOYSA-N 0.000 description 1
- 229940099259 vaseline Drugs 0.000 description 1
- NLVXSWCKKBEXTG-UHFFFAOYSA-N vinylsulfonic acid Chemical compound OS(=O)(=O)C=C NLVXSWCKKBEXTG-UHFFFAOYSA-N 0.000 description 1
- 229930003231 vitamin Natural products 0.000 description 1
- 235000013343 vitamin Nutrition 0.000 description 1
- 239000011782 vitamin Substances 0.000 description 1
- 229940088594 vitamin Drugs 0.000 description 1
- 238000010792 warming Methods 0.000 description 1
- 238000005303 weighing Methods 0.000 description 1
- 239000010497 wheat germ oil Substances 0.000 description 1
- 230000029663 wound healing Effects 0.000 description 1
- 239000012138 yeast extract Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/38—Cationic compounds
- C11D1/62—Quaternary ammonium compounds
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
- A61K47/06—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite
- A61K47/16—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite containing nitrogen, e.g. nitro-, nitroso-, azo-compounds, nitriles, cyanates
- A61K47/18—Amines; Amides; Ureas; Quaternary ammonium compounds; Amino acids; Oligopeptides having up to five amino acids
- A61K47/186—Quaternary ammonium compounds, e.g. benzalkonium chloride or cetrimide
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
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- A61K8/02—Cosmetics or similar toiletry preparations characterised by special physical form
- A61K8/04—Dispersions; Emulsions
- A61K8/06—Emulsions
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/31—Hydrocarbons
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
- A61K8/37—Esters of carboxylic acids
- A61K8/375—Esters of carboxylic acids the alcohol moiety containing more than one hydroxy group
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/40—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
- A61K8/41—Amines
- A61K8/416—Quaternary ammonium compounds
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/40—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
- A61K8/44—Aminocarboxylic acids or derivatives thereof, e.g. aminocarboxylic acids containing sulfur; Salts; Esters or N-acylated derivatives thereof
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/63—Steroids; Derivatives thereof
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/10—Dispersions; Emulsions
- A61K9/107—Emulsions ; Emulsion preconcentrates; Micelles
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q19/00—Preparations for care of the skin
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- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/38—Cationic compounds
- C11D1/65—Mixtures of anionic with cationic compounds
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- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
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Abstract
Description
(カチオンとアニオンの少なくともいずれかに水素結合性官能基を有する有機アンモニウム塩)
本発明において有機アンモニウム塩は、窒素原子をイオン中心とする有機カチオンまたはNH4 +、および/または有機アニオンを含む。
以上のポリヒドロキシアルキル基の中でも、2,3−ジヒドロキシプロパン−1−イル基、1,3−ジヒドロキシプロパン−2−イル基、1,3−ジヒドロキシ−2−エチルプロパン−2−イル基、1,3−ジヒドロキシ−2−ヒドロキシメチルプロパン−2−イル基、ペンタヒドロキシヘキサン−1−イル基が好ましい。
前記飽和脂肪族カルボン酸アニオンは、直鎖状又は分岐鎖状の脂肪族飽和炭化水素基と1個以上のカルボン酸アニオンからなり、カルボキシ基、カルボキシレート基を含んでも良く、炭素数1〜22が好ましい。具体的には、特に限定されないが、例えば、蟻酸、酢酸、プロピオン酸、酪酸、吉草酸、カプロン酸、エナント酸、カプリル酸、ペラルゴン酸、カプリン酸、ラウリン酸、ミリスチン酸、ペンタデシル酸、パルミチン酸、マルガリン酸、ステアリン酸、アラキジン酸、ヘンイコシル酸、ベヘン酸、イソ酪酸、2−メチル酪酸、イソ吉草酸、2−エチルヘキサン酸、イソノナン酸、イソパルミチン酸、イソステアリン酸、シュウ酸、マロン酸、コハク酸、グルタル酸、アジピン酸、ピメリン酸、スベリン酸、アゼライン酸、セバシン酸等からプロトンが解離したアニオンが挙げられる。
(界面活性剤)
本発明の組成物に含まれる界面活性剤は、特に限定されず、一般的な界面活性剤を使用することができる。界面活性剤としては、非イオン界面活性剤、アニオン界面活性剤、カチオン界面活性剤、および両性イオン界面活性剤、シリコーン系界面活性剤から適宜選択して用いることができ、その中でも、非イオン界面活性剤、アニオン界面活性剤が好ましく、特に油中水型(W/O)乳化組成物の場合、非イオン界面活性剤が好ましい。これらは1種単独で使用してもよく、2種以上を組み合わせて使用してもよい。
本発明の組成物の形状は、成分が分離しなければ特に限定されないが、均一な組成物、乳化組成物が好ましく、液状組成物、ゲル状組成物、油中水型(W/O型)乳化組成物、水中油型(O/W型)乳化組成物、複合型エマルション(W/O/W型、O/W/O型)等とすることができる。
本発明において、有機アンモニウム塩、界面活性剤および油剤を含む組成物に使用される、有機アンモニウム塩、界面活性剤は、上記に挙げたものが使用できる。油剤としては、特に限定されず、例えば、炭化水素類、油脂類、エステル類、脂肪酸類、高級アルコール類、シリコーン油類、ロウ類、ステロイド類、モノマー、オリゴマー、流動性のあるポリマー(高分子化合物)、シリコーン油、アルコール類、グリコール類、グリコールエーテル類、セロソルブ類等が挙げられ、これらは常温で液体、ゲル、固体のいずれであってもよい。これらは1種単独で使用してもよく、2種以上を組み合わせて使用してもよい。
本発明において、乳化組成物は、特に限定されず、油中水型(W/O型)乳化組成物、水中油型(O/W型)乳化組成物、複合型エマルション(W/O/W型、O/W/O型)等が挙げられる。
<有機アンモニウム塩>
表1〜12に示す化合物1〜21の化合物は以下の方法で合成、入手した。
化合物1、2、4〜20、22〜27:特開2014−131975号公報に記載の方法で合成した。
各化合物の構造は表3に記載。なお、水和物については、その含水率を表3に示した。
化合物3:1−(2−ヒドロキシエチル)−3−メチルイミダゾリウムクロリドは、東京化成工業(株) 製の試薬を用いた。
化合物21:テトラブチルアンモニウムブロミドは、東京化成工業(株) 製の試薬を用いた。
<界面活性剤>
トリステアリン酸ソルビタンは、日光ケミカルズ(株)製のNIKKOL SS-30Vを用いた。
ペンタイソステアリン酸デカグリセリルは、日光ケミカルズ(株)製のNIKKOL DECAGLYN 5-ISVを用いた。
セスキイソステアリン酸ソルビタンは、日光ケミカルズ(株)製のNIKKOL SI-15RVを用いた。
モノオレイン酸ジグリセリルは、日光ケミカルズ(株)製のNIKKOL DGMO-CVを用いた。
POE(6)ソルビットミツロウは、日光ケミカルズ(株)製のNIKKOL GBW-25を用いた。
テトラオレイン酸POE(6)ソルビットは、日光ケミカルズ(株)製のNIKKOL GO-4Vを用いた。
デオキシコール酸ナトリウムは、富士フイルム和光純薬(株)製を用いた。
<油剤>
流動パラフィンは、富士フイルム和光純薬(株)製の試薬を用いた。
スクワランは、日光ケミカルズ(株)製を用いた。
セレシンは、日興リカ(株)製を用いた。
白色ワセリンは、富士フイルム和光純薬(株)製の試薬を用いた。
ドデシルベンゼンは、東京化成工業(株)製の試薬を用いた。
パルミチン酸2−エチルヘキシルは、富士フイルム和光純薬(株)製の試薬を用いた。
トリトメット酸トリス(2−エチルヘキシル)は、東京化成工業(株)製の試薬を用いた。
<その他>
グリセリンは、関東化学(株)製の試薬を用いた。
乳酸カリウムは、関東化学(株)製の試薬を用いた。
乳酸ナトリウムは、関東化学(株)製の試薬を用いた。
グルタミン酸は、富士フイルム和光純薬(株)製の試薬を用いた。
没食子酸は、シグマアルドリッチ製の試薬を用いた。
1−1.組成物の外観
表1に示す組成に従い、実施例1〜11、比較例1の組成物を調製した。すべての成分を秤量後、80℃で3分間攪拌し、混合させ組成物を得た。
2−1.組成物の外観
表2に示す組成に従い、実施例12〜25の組成物、及び比較例2〜5の組成物を調製した。具体的には、界面活性剤と油剤を80℃に加熱し均一に溶解させた。次いで、温度を保ちながら有機アンモニウム塩を徐々に添加し、80℃で3分間攪拌、混合させた。その後、乳化物を25℃まで冷却し、組成物を得た。
3.1.油中水型(W/O型)乳化組成物
表3〜6に示す組成に従い、実施例26〜67、比較例6〜12の組成で乳化および乳化組成物の安定性の評価を行った。具体的には、油剤、界面活性剤を80℃に加熱し、均一に溶解させた。次いで、有機アンモニウム塩と水を均一溶解させたものを、温度を保ちながら徐々に添加し、3分間80℃で攪拌し、25℃に冷却した。なお、得られた乳化組成物は、電気伝導度を測定した結果、電気伝導度が低く、連続相が油相であり、得られた乳化組成物はW/O型乳化物と判断した。
<乳化状態の確認>
実施例26〜67、比較例6〜12の組成物の外観を目視により乳化の形成を確認した。乳化状態が良好なものは〇、分離しているものは×と評価した。
<乳化組成物安定性1>
得られた乳化組成物を50℃に調整された恒温槽に1週間保管し、乳化状態の変化について下記の基準で確認を行った。
<乳化組成物安定性2>
得られた乳化組成物を遠心分離機を用い2700rpm、13500rpmで1時間遠心分離を行い、乳化安定性を下記の基準で評価した。
〇:乳化状態が良好に保持
△:乳化状態は維持しているが、多少分離
×:乳化状態が崩壊し、完全に分離
<有効成分の溶解性評価>
表7に記載の組成に対する有効成分の溶解性を評価した。有効成分としては、難溶性の抗酸化作用を有する没食子酸、保湿作用を有するグルタミン酸を用いた。グルタミン酸を溶解した比較例14(グリセリン水溶液),15(水)は、溶解度が0.08g未満であったが、実施例68は、0.24gと高い溶解度であった。また、同様に没食子酸を溶解した比較例17,18は、溶解度が0.08gであったが、実施例69は、0.32gと高い溶解度であった。さらに、カチオンに水素結合性を有さない比較例13,16は、実施例68,69より低溶解性であった。以上の結果より本発明の水素結合性官能基を有する有機アンモニウム塩は、有効成分をより多く溶解した。
表8で溶解した有機アンモニウム塩/水を油剤、界面活性剤と混合して、乳化状態を確認した。乳化状態が良好なものは〇、分離しているものは×と評価した。評価の結果、良好に乳化できた。実施例は、高濃度で有効成分を配合した乳化組成物が得られ、本発明の水素結合性官能基を有する有機アンモニウム塩を含む組成物は、有効成分をより多く配合することが可能で、溶媒、キャリアーとして有用であることを確認した。
<保水性>
表9に示すように実施例72〜81、比較例19〜28の乳化組成物をバイアル瓶に0.2g秤量し、80℃に調整された恒温槽に2.5時間保管し、水分量の減少率を算出した。
<使用感>
乳化組成物を一定量肌にのせて、乳化組成物を塗布時の伸び、べとつき、保湿感、肌なじみついて評価を行った。
<表面抵抗値測定>
表面抵抗値測定は乳化調整前の化合物1ならびにグリセリンと乳化調整後の乳化組成物について実施した。乳化調整前の有機塩の化合物1ならびにグリセリンの比較では、化合物1およびグリセリンの0.7g(無水物に換算した含有量)をそれぞれポリウレタン製人工皮革に塗布し、高抵抗計(東京電子株式会社製、スタックTR−2)を用いて表面抵抗値を測定した。また、乳化組成物による比較では、表11の乳化組成物0.05gをそれぞれポリウレタン製人工皮革に塗布し、高抵抗計を用いて表面抵抗値を測定した。
3.2.水中油型(O/W型)乳化組成物
<乳化状態の確認、乳化組成物安定性1、乳化組成物安定性2>
表12に示す組成に従い、実施例93の乳化組成物、及び比較例40、41の乳化組成物を調製した。具体的には、室温で、有機アンモニウム塩または濃グリセリンを、水に均一に溶解させた。次いで、油剤を徐々に添加し、その後3分間攪拌した。なお、得られた乳化物は、電気伝導度を測定した結果、水と同等の電気伝導度が得られ、連続相が水相であることが確認でき、得られた乳化物はO/W型乳化物と判断した。
表13に示す組成に従い、実施例94〜101の組成で乳化および乳化組成物の安定性の評価を行った。具体的には、油剤、界面活性剤を80℃に加熱し、均一に溶解させた。次いで、有機アンモニウム塩と染料(Daiwa Black 2H)と水を均一溶解させたものを、温度を保ちながら徐々に添加し、3分間80℃で攪拌し、25℃に冷却した。なお、得られた乳化組成物は、電気伝導度を測定した結果、電気伝導度が低く、連続相が油相であり、得られた乳化組成物はW/O型乳化物と判断した。得られた組成物の乳化状態の評価は、乳化状態が良好なものは〇、分離しているものは×と評価した。
Claims (15)
- カチオンとアニオンの少なくともいずれかに水素結合性官能基を有する有機アンモニウム塩と界面活性剤を含む、組成物。
- 前記カチオンがアンモニウムカチオンである請求項1に記載の組成物。
- 前記カチオンが次式(I):
- nは1〜4の整数である請求項3に記載の組成物。
- R1が炭素数1〜10で直鎖状もしくは分岐鎖状のモノヒドロキシアルキル基、モノカルボキシアルキル基もしくはモノヒドロキシカルボキシアルキル基であり、nが1〜4の整数である請求項4に記載の組成物。
- R2が水素原子である請求項5に記載の組成物。
- R2が炭素数1〜18の直鎖状もしくは分岐状のアルキル基である請求項5に記載の組成物。
- R1のうち少なくとも1つが水酸基を2個以上有する炭素数1〜10で直鎖状もしくは分岐鎖状のポリヒドロキシアルキル基であり、nが1〜4の整数である請求項4に記載の組成物。
- R2が水素原子である請求項8に記載の組成物。
- 前記アニオンがカルボン酸系アニオンである請求項1〜9のいずれか一項に記載の組成物。
- アニオンに水素結合性官能基を有する請求項1〜10のいずれか一項に記載の組成物。
- 前記水素結合性官能基が、水酸基、カルボキシ基、カルボキシレート基のいずれかである請求項11に記載の組成物。
- 前記組成物に、さらに油剤を含む請求項1〜12のいずれか一項に記載の組成物。
- 前記組成物に、さらに水を含み、前記組成物が乳化組成物である、請求項13に記載の組成物。
- 前記有機アンモニウム塩の無水物および水和物が、25℃で液体である請求項1〜14のいずれか一項に記載の組成物。
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