JP4696534B2 - 油性基剤のゲル化剤 - Google Patents
油性基剤のゲル化剤 Download PDFInfo
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- JP4696534B2 JP4696534B2 JP2004328261A JP2004328261A JP4696534B2 JP 4696534 B2 JP4696534 B2 JP 4696534B2 JP 2004328261 A JP2004328261 A JP 2004328261A JP 2004328261 A JP2004328261 A JP 2004328261A JP 4696534 B2 JP4696534 B2 JP 4696534B2
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- 239000002537 cosmetic Substances 0.000 claims description 25
- 125000004432 carbon atom Chemical group C* 0.000 claims description 20
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- 239000003213 antiperspirant Substances 0.000 claims description 17
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- 229930195734 saturated hydrocarbon Natural products 0.000 claims description 11
- 239000003795 chemical substances by application Substances 0.000 claims description 9
- 238000001879 gelation Methods 0.000 claims description 8
- 229930195735 unsaturated hydrocarbon Natural products 0.000 claims description 8
- 229910052799 carbon Inorganic materials 0.000 claims description 3
- 150000001721 carbon Chemical group 0.000 claims description 2
- 125000001183 hydrocarbyl group Chemical group 0.000 claims 3
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- 239000000654 additive Substances 0.000 description 3
- 150000003973 alkyl amines Chemical class 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
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- FMZUHGYZWYNSOA-VVBFYGJXSA-N (1r)-1-[(4r,4ar,8as)-2,6-diphenyl-4,4a,8,8a-tetrahydro-[1,3]dioxino[5,4-d][1,3]dioxin-4-yl]ethane-1,2-diol Chemical compound C([C@@H]1OC(O[C@@H]([C@@H]1O1)[C@H](O)CO)C=2C=CC=CC=2)OC1C1=CC=CC=C1 FMZUHGYZWYNSOA-VVBFYGJXSA-N 0.000 description 2
- KIUKXJAPPMFGSW-DNGZLQJQSA-N (2S,3S,4S,5R,6R)-6-[(2S,3R,4R,5S,6R)-3-Acetamido-2-[(2S,3S,4R,5R,6R)-6-[(2R,3R,4R,5S,6R)-3-acetamido-2,5-dihydroxy-6-(hydroxymethyl)oxan-4-yl]oxy-2-carboxy-4,5-dihydroxyoxan-3-yl]oxy-5-hydroxy-6-(hydroxymethyl)oxan-4-yl]oxy-3,4,5-trihydroxyoxane-2-carboxylic acid Chemical compound CC(=O)N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O)[C@@H]1O[C@H]1[C@H](O)[C@@H](O)[C@H](O[C@H]2[C@@H]([C@@H](O[C@H]3[C@@H]([C@@H](O)[C@H](O)[C@H](O3)C(O)=O)O)[C@H](O)[C@@H](CO)O2)NC(C)=O)[C@@H](C(O)=O)O1 KIUKXJAPPMFGSW-DNGZLQJQSA-N 0.000 description 2
- UFHPNDQJPUDPHI-NSHDSACASA-N (4s)-4-amino-5-(dibutylamino)-5-oxopentanoic acid Chemical compound CCCCN(CCCC)C(=O)[C@@H](N)CCC(O)=O UFHPNDQJPUDPHI-NSHDSACASA-N 0.000 description 2
- VBICKXHEKHSIBG-UHFFFAOYSA-N 1-monostearoylglycerol Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(O)CO VBICKXHEKHSIBG-UHFFFAOYSA-N 0.000 description 2
- WNWHHMBRJJOGFJ-UHFFFAOYSA-N 16-methylheptadecan-1-ol Chemical compound CC(C)CCCCCCCCCCCCCCCO WNWHHMBRJJOGFJ-UHFFFAOYSA-N 0.000 description 2
- XDOFQFKRPWOURC-UHFFFAOYSA-N 16-methylheptadecanoic acid Chemical compound CC(C)CCCCCCCCCCCCCCC(O)=O XDOFQFKRPWOURC-UHFFFAOYSA-N 0.000 description 2
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- ZNVKGUVDRSSWHV-UHFFFAOYSA-L zinc;4-hydroxybenzenesulfonate Chemical compound [Zn+2].OC1=CC=C(S([O-])(=O)=O)C=C1.OC1=CC=C(S([O-])(=O)=O)C=C1 ZNVKGUVDRSSWHV-UHFFFAOYSA-L 0.000 description 1
- 229910001928 zirconium oxide Inorganic materials 0.000 description 1
- IPCAPQRVQMIMAN-UHFFFAOYSA-L zirconyl chloride Chemical compound Cl[Zr](Cl)=O IPCAPQRVQMIMAN-UHFFFAOYSA-L 0.000 description 1
- 239000004711 α-olefin Substances 0.000 description 1
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- Cosmetics (AREA)
Description
下記一般式(B):
7〜17の炭化水素基を示す)で表される化合物(B)の少なくとも一種とを含有する、油性基剤のゲル化剤を提供するものである。
N−ラウロイルグルタミン酸−γ−メチルエステル(6.8g,0.02mol)をトルエン(10g)に溶解しブチルアミン(9g,0.12mol)を添加し、90℃で4時間反応させた。水を加えた後硫酸で中和後抽出し、溶媒を留去してγ−ブチルアミドを得た。これを6gとり窒素下で160℃、6.5時間反応させた後、酢酸エチル、NaOH水溶液を加え抽出を行い、Na2SO4、MgSO4で脱水後溶媒を留去して反応物を得た。これをPTLC(酢酸エチル:ヘキサン=1:2)により精製し、目的物であるN−ブチル−2−(N’−ラウロイルアミノ)グルタルイミドを得た。
化合物(A)としてN−ブチル−2−(N’−ラウロイルアミノ) グルタルイミド 0.0005重量部、化合物(B)としてN−ラウロイル−L−グルタミン酸 ジブチルアミド0.1995重量部を、油性基剤(b)としてのn−トリデカン20重量部に入れ、150℃のオイルバスで加熱溶解し、15時間、23℃で放冷し、ゲル状組成物を得た。
化合物(A)、化合物(B)および油性基剤(b)を、表1に示す配合量用いたこと以外は、実施例1と同様に行い、それぞれゲル状組成物を得た。
実施例および比較例のゲル状組成物のゲル強度をレオメータ(FUDOH RHEO METER NRM−2010−J−CW)にて測定した。アダプターはプルーム用・粘弾性用、10φを用い、試料台速度は6cm/minとした。そのゲル強度値が90g/cm2以上のときを○、70〜90g/cm2のときを△、70g/cm2未満のときを×とした。結果を表1に示す。
実施例および比較例のゲル状組成物を皮膚に塗布した時の延展性につき、以下の評価基準に基づき専門パネラー5人により評価した。
5:非常に延展性に優れる
4:延展性に優れる
3:普通
2:延展性に劣る
1:非常に延展性に劣る
その評価結果の平均点が4.5以上を◎、3.5〜4.4を○、2.5〜3.4のときを△、2.4以下の時を×とした。結果を表1に示す。
1)N−ブチル−2−(N’−ラウロイルアミノ) グルタルイミド 0.02g
2)N−ラウロイル−L−グルタルミン酸 ジブチルアミド 1.0 g
3)N−2−エチルヘキサノイル−L−グルタミン酸 ジブチルアミド 1.0 g
4)2−エチルヘキサン酸 ブチルアミド 0.01g
5)12−ヒドロキシステアリン酸 7.0 g
6)オクチルドデカノール 14.0 g
7)シクロメチコンD−5(東レダウコーニング社製 SH245) 48.0 g
8)アルミニウムジルコニウムトリクロロハイドレックスグリシン(ウエストウッド・ケミカル・コーポレーション Westchlor ZR 30B DM CP-5) 26.0 g
Claims (8)
- 化合物(B)100重量部に対する化合物(A)の含有量が、0.1重量部以上50重量部以下であることを特徴とする請求項1記載の化粧料用油性基剤のゲル化剤。
- 化合物(B)100重量部に対する化合物(A)の含有量が、0.5重量部以上50重量部以下であることを特徴とする請求項1記載の化粧料用油性基剤のゲル化剤。
- 化合物(B)100重量部に対する化合物(A)の含有量が、1重量部以上50重量部以下であることを特徴とする請求項1記載の化粧料用油性基剤のゲル化剤。
- 化合物(B)100重量部に対する化合物(A)の含有量が、2重量部以上50重量部以下であることを特徴とする請求項1記載の化粧料用油性基剤のゲル化剤。
- (a)請求項1〜5のいずれかに記載のゲル化剤、及び(b)少なくとも1種の油性基剤を含有するゲル状組成物。
- さらに(c)少なくとも1種の制汗活性成分を含有する請求項6に記載のゲル状組成物。
- 請求項6または7記載のゲル状組成物を含む化粧料。
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JP4871640B2 (ja) * | 2006-05-17 | 2012-02-08 | 花王株式会社 | 環状イミド化合物 |
JP2012035233A (ja) * | 2010-08-11 | 2012-02-23 | Seiko Epson Corp | ゲル形成性溶液及びゲル製造方法 |
EP4159823A1 (en) | 2016-10-24 | 2023-04-05 | Ajinomoto Co., Inc. | Gel composition comprising a glutamide |
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Citations (3)
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JPS5119139A (ja) * | 1974-08-07 | 1976-02-16 | Ajinomoto Kk | Gerujokeshoryososeibutsu |
JPH07506833A (ja) * | 1992-05-12 | 1995-07-27 | ザ、プロクター、エンド、ギャンブル、カンパニー | 発汗抑制ゲルスティック組成物 |
JP2002316971A (ja) * | 2001-02-13 | 2002-10-31 | Ajinomoto Co Inc | 油性基剤のゲル化剤 |
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JPS5119139A (ja) * | 1974-08-07 | 1976-02-16 | Ajinomoto Kk | Gerujokeshoryososeibutsu |
JPH07506833A (ja) * | 1992-05-12 | 1995-07-27 | ザ、プロクター、エンド、ギャンブル、カンパニー | 発汗抑制ゲルスティック組成物 |
JP2002316971A (ja) * | 2001-02-13 | 2002-10-31 | Ajinomoto Co Inc | 油性基剤のゲル化剤 |
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