JP6653910B1 - ゲル状洗浄剤 - Google Patents
ゲル状洗浄剤 Download PDFInfo
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- JP6653910B1 JP6653910B1 JP2019134556A JP2019134556A JP6653910B1 JP 6653910 B1 JP6653910 B1 JP 6653910B1 JP 2019134556 A JP2019134556 A JP 2019134556A JP 2019134556 A JP2019134556 A JP 2019134556A JP 6653910 B1 JP6653910 B1 JP 6653910B1
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- acid
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- sodium
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- LRBQNJMCXXYXIU-NRMVVENXSA-N tannic acid Chemical compound OC1=C(O)C(O)=CC(C(=O)OC=2C(=C(O)C=C(C=2)C(=O)OC[C@@H]2[C@H]([C@H](OC(=O)C=3C=C(OC(=O)C=4C=C(O)C(O)=C(O)C=4)C(O)=C(O)C=3)[C@@H](OC(=O)C=3C=C(OC(=O)C=4C=C(O)C(O)=C(O)C=4)C(O)=C(O)C=3)[C@@H](OC(=O)C=3C=C(OC(=O)C=4C=C(O)C(O)=C(O)C=4)C(O)=C(O)C=3)O2)OC(=O)C=2C=C(OC(=O)C=3C=C(O)C(O)=C(O)C=3)C(O)=C(O)C=2)O)=C1 LRBQNJMCXXYXIU-NRMVVENXSA-N 0.000 description 1
- 235000015523 tannic acid Nutrition 0.000 description 1
- 229940033123 tannic acid Drugs 0.000 description 1
- 229920001864 tannin Polymers 0.000 description 1
- 235000018553 tannin Nutrition 0.000 description 1
- 239000001648 tannin Substances 0.000 description 1
- NHGXDBSUJJNIRV-UHFFFAOYSA-M tetrabutylammonium chloride Chemical compound [Cl-].CCCC[N+](CCCC)(CCCC)CCCC NHGXDBSUJJNIRV-UHFFFAOYSA-M 0.000 description 1
- BSYVTEYKTMYBMK-UHFFFAOYSA-N tetrahydrofurfuryl alcohol Chemical compound OCC1CCCO1 BSYVTEYKTMYBMK-UHFFFAOYSA-N 0.000 description 1
- KWXLCDNSEHTOCB-UHFFFAOYSA-J tetrasodium;1,1-diphosphonatoethanol Chemical compound [Na+].[Na+].[Na+].[Na+].[O-]P(=O)([O-])C(O)(C)P([O-])([O-])=O KWXLCDNSEHTOCB-UHFFFAOYSA-J 0.000 description 1
- UEUXEKPTXMALOB-UHFFFAOYSA-J tetrasodium;2-[2-[bis(carboxylatomethyl)amino]ethyl-(carboxylatomethyl)amino]acetate Chemical compound [Na+].[Na+].[Na+].[Na+].[O-]C(=O)CN(CC([O-])=O)CCN(CC([O-])=O)CC([O-])=O UEUXEKPTXMALOB-UHFFFAOYSA-J 0.000 description 1
- SHWIJIJNPFXOFS-UHFFFAOYSA-N thiotaurine Chemical compound NCCS(O)(=O)=S SHWIJIJNPFXOFS-UHFFFAOYSA-N 0.000 description 1
- 229930003799 tocopherol Natural products 0.000 description 1
- 239000011732 tocopherol Substances 0.000 description 1
- 229940042585 tocopherol acetate Drugs 0.000 description 1
- 235000019149 tocopherols Nutrition 0.000 description 1
- 229950009883 tocopheryl nicotinate Drugs 0.000 description 1
- JIVZKJJQOZQXQB-UHFFFAOYSA-N tolazoline Chemical compound C=1C=CC=CC=1CC1=NCCN1 JIVZKJJQOZQXQB-UHFFFAOYSA-N 0.000 description 1
- 229960002312 tolazoline Drugs 0.000 description 1
- 229940074410 trehalose Drugs 0.000 description 1
- ILJSQTXMGCGYMG-UHFFFAOYSA-N triacetic acid Chemical compound CC(=O)CC(=O)CC(O)=O ILJSQTXMGCGYMG-UHFFFAOYSA-N 0.000 description 1
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 1
- JLGLQAWTXXGVEM-UHFFFAOYSA-N triethylene glycol monomethyl ether Chemical compound COCCOCCOCCO JLGLQAWTXXGVEM-UHFFFAOYSA-N 0.000 description 1
- PUVAFTRIIUSGLK-UHFFFAOYSA-M trimethyl(oxiran-2-ylmethyl)azanium;chloride Chemical compound [Cl-].C[N+](C)(C)CC1CO1 PUVAFTRIIUSGLK-UHFFFAOYSA-M 0.000 description 1
- MQAYPFVXSPHGJM-UHFFFAOYSA-M trimethyl(phenyl)azanium;chloride Chemical compound [Cl-].C[N+](C)(C)C1=CC=CC=C1 MQAYPFVXSPHGJM-UHFFFAOYSA-M 0.000 description 1
- KMVDECFGXJKYHV-UHFFFAOYSA-L trimethyl-[10-(trimethylazaniumyl)decyl]azanium;dichloride Chemical compound [Cl-].[Cl-].C[N+](C)(C)CCCCCCCCCC[N+](C)(C)C KMVDECFGXJKYHV-UHFFFAOYSA-L 0.000 description 1
- 229960005066 trisodium edetate Drugs 0.000 description 1
- XPFJYKARVSSRHE-UHFFFAOYSA-K trisodium;2-hydroxypropane-1,2,3-tricarboxylate;2-hydroxypropane-1,2,3-tricarboxylic acid Chemical compound [Na+].[Na+].[Na+].OC(=O)CC(O)(C(O)=O)CC(O)=O.[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O XPFJYKARVSSRHE-UHFFFAOYSA-K 0.000 description 1
- SOBHUZYZLFQYFK-UHFFFAOYSA-K trisodium;hydroxy-[[phosphonatomethyl(phosphonomethyl)amino]methyl]phosphinate Chemical compound [Na+].[Na+].[Na+].OP(O)(=O)CN(CP(O)([O-])=O)CP([O-])([O-])=O SOBHUZYZLFQYFK-UHFFFAOYSA-K 0.000 description 1
- 239000006097 ultraviolet radiation absorber Substances 0.000 description 1
- LNRUEZIDUKQGRH-YZUCMPLFSA-N umbelliferose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O[C@@H]2[C@@H]([C@@H](O)[C@@H](O)[C@@H](CO)O2)O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 LNRUEZIDUKQGRH-YZUCMPLFSA-N 0.000 description 1
- FLUADVWHMHPUCG-SWPIJASHSA-N verbascose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO[C@@H]2[C@@H]([C@@H](O)[C@@H](O)[C@@H](CO[C@@H]3[C@@H]([C@@H](O)[C@@H](O)[C@@H](CO[C@@H]4[C@@H]([C@@H](O)[C@@H](O)[C@@H](CO)O4)O)O3)O)O2)O)O1 FLUADVWHMHPUCG-SWPIJASHSA-N 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 239000011719 vitamin A Substances 0.000 description 1
- 235000019155 vitamin A Nutrition 0.000 description 1
- 235000010374 vitamin B1 Nutrition 0.000 description 1
- 239000011691 vitamin B1 Substances 0.000 description 1
- 235000019164 vitamin B2 Nutrition 0.000 description 1
- 239000011716 vitamin B2 Substances 0.000 description 1
- 235000019158 vitamin B6 Nutrition 0.000 description 1
- 239000011726 vitamin B6 Substances 0.000 description 1
- 235000019165 vitamin E Nutrition 0.000 description 1
- 239000011709 vitamin E Substances 0.000 description 1
- 239000009538 yokuinin Substances 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
- OJYLAHXKWMRDGS-UHFFFAOYSA-N zingerone Chemical compound COC1=CC(CCC(C)=O)=CC=C1O OJYLAHXKWMRDGS-UHFFFAOYSA-N 0.000 description 1
- 239000004711 α-olefin Substances 0.000 description 1
- LTVDFSLWFKLJDQ-UHFFFAOYSA-N α-tocopherolquinone Chemical compound CC(C)CCCC(C)CCCC(C)CCCC(C)(O)CCC1=C(C)C(=O)C(C)=C(C)C1=O LTVDFSLWFKLJDQ-UHFFFAOYSA-N 0.000 description 1
- FYGDTMLNYKFZSV-BYLHFPJWSA-N β-1,4-galactotrioside Chemical compound O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@H]1O[C@@H]1[C@H](CO)O[C@@H](O[C@@H]2[C@@H](O[C@@H](O)[C@H](O)[C@H]2O)CO)[C@H](O)[C@H]1O FYGDTMLNYKFZSV-BYLHFPJWSA-N 0.000 description 1
- 229930007845 β-thujaplicin Natural products 0.000 description 1
- QUEDXNHFTDJVIY-UHFFFAOYSA-N γ-tocopherol Chemical class OC1=C(C)C(C)=C2OC(CCCC(C)CCCC(C)CCCC(C)C)(C)CCC2=C1 QUEDXNHFTDJVIY-UHFFFAOYSA-N 0.000 description 1
Classifications
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- A—HUMAN NECESSITIES
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- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
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- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
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- 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
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- C11D1/04—Carboxylic acids or salts thereof
- C11D1/06—Ether- or thioether carboxylic acids
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Abstract
Description
これに対し、カチオン化キサンタンガムを用いて離漿を防止するとともに、pHを下げて褐変を防止する技術が、本発明者らにより提案されている(特許文献4)。
しかしながら、前記特許文献4に示すゲル状洗浄剤にあっても、これらの点には改善の余地が残されていた。
本発明は前記従来技術の課題に鑑みなされたものであり、その目的はpH7.5以下で、しかも泡立ち性に優れたゲル状洗浄剤を提供することにある。
ポリオキシエチレンアルキルエーテルカルボン酸塩2〜11質量%と、
キシログルカン0.5〜3質量%と、
カチオン化キサンタンガム0.2〜3質量%と、を含み、
1%水溶液のpHが7.5以下であることを特徴とする。
また、前記ゲル状洗浄剤において、さらに脱アシル型ジェランガム0.01〜0.5質量%含むことが好適である。
また、前記ゲル状洗浄剤において、ポリオキシエチレンアルキルエーテルカルボン酸塩は、POE(3〜5)ラウリルエーテルカルボン酸であることが好適である。
また、前記ゲル状洗浄剤において、ポリオキシエチレンアルキルエーテルカルボン酸塩の中和率は60〜90%であることが好適である。
(A)ポリオキシエチレンアルキルエーテルカルボン酸塩
本発明のゲル状洗浄剤に主洗浄剤として配合されるポリオキシアルキルエーテルカルボン酸塩は、低刺激性のアニオン界面活性剤であり、以下の構造を有する。
R−O−(CH2CH2O)nCH2COOM
R:炭素数12〜18の飽和アルキル基
M:Na,K,アミン、2−アミノ−2−ヒドロキシメチル-1,3−プロパンジオール等
n:平均0〜20 好ましくは平均3〜5
特にRがラウリル基であるポリオキシラウリルエーテルカルボン酸塩が好ましい。
本発明において採用されるポリオキシエチレンアルキルエーテルカルボン酸は、pH7前後の領域で優れた溶解性、洗浄性を有するとともに、キシログルカンによるゲル状洗浄剤として、高い起泡性を発揮することができる。
これに対しポリオキシエチレンアルキルエーテルカルボン酸塩は、理論モル量以下の対イオン添加でも十分な溶解性、洗浄性を発揮することができ、しかも優れた泡立ち性が得られる。本発明者らの検討によれば、理論モル量の60%〜90%程度の対イオン量でも必要な機能が発揮される。
この結果、系全体のpHを低く(pH7.5以下)抑えることが可能となり、変色抑制、スティンギング刺激の低減、肌に対するマイルド感の向上を図ることができる。
本発明におけるポリオキシエチレンアルキルエーテルカルボン酸塩の配合量は、洗浄性の観点から組成物に対し2〜11質量%であることが好ましい。
本発明のゲル状洗浄剤に配合されるキシログルカンは、主に熱帯地方に産する豆科植物であるタマリンダス・インディカ(Tamarindus indica) の種子の主成分であり、下記式(I)で表わされる、β−1,4グルカンからなる主鎖の一部に、側鎖としてキシロースがα−1,6結合し、キシロースの一部にはガラクトースが結合した構造を有する、分子量が数十万の多糖である。
本発明に用いるカチオン化キサンタンガムは、キサンタンガムをカチオン化変性した水溶性高分子である。キサンタンガムは、下記式(II)に示すような構造である。
本発明において、脱アシル型ジェランガムを配合することが好ましい。
本発明において好適に用いられる脱アシル型ジェランガムは、微生物スフィンゴモナス・エロディア(Sphingomonas elodea)がブドウ糖などを栄養源として菌体外に蓄積した多糖類を、分離・精製してジェランガムを得、アシル基を除去して脱アシル型ジェランガムが得られる。
前記脱アシル型ジェランガムは、主鎖に2個のグルコース、1個のグルクロン酸、1個のラムノースの4糖が結合した、下記構成をとる。
本発明において、脱アシル型ジェランガムの配合量は、組成物中0.01〜0.5質量%が好ましく、さらに好ましくは0.05〜0.1質量%である。
上記(A)〜(C) 成分を含むゲル状洗浄剤を製造するにあたっては、製造釜に、水、石鹸等の界面活性剤を仕込み加熱溶解後、グリコール等で湿潤分散したキシログルカンを添加して攪拌溶解。その後、グリセリン等を加えて増粘させ冷却する。
本発明にかかるゲル状洗浄剤には、本発明の効果を損なわない範囲において、他の成分、例えば、アニオン性界面活性剤、カチオン性界面活性剤、両性界面活性剤、非イオン性界面活性剤、保湿剤、水溶性高分子、増粘剤、皮膜剤、紫外線吸収剤、金属イオン封鎖剤、低級アルコール、多価アルコール、油分、糖、アミノ酸、有機アミン、高分子エマルジョン、pH調整剤、皮膚栄養剤、ビタミン、酸化防止剤、酸化防止助剤、香料、着色剤、水等を必要に応じて適宜配合し、目的とする剤形に応じて製造することが出来る。
高分子エマルジョンとしては、例えば、アクリル樹脂エマルジョン、ポリアクリル酸エチルエマルジョン、アクリルレジン液、ポリアクリルアルキルエステルエマルジョン、ポリ酢酸ビニル樹脂エマルジョン、天然ゴムラテックス等が挙げられる。
ビタミン類としては、例えば、ビタミンA、B1、B2、B6、C、E及びその誘導体、パントテン酸及びその誘導体、ビオチン等が挙げられる。
酸化防止剤としては、例えば、トコフェロール類、ジブチルヒドロキシトルエン、ブチルヒドロキシアニソール、没食子酸エステル類等が挙げられる。
なお、以下の実施例において、評価は以下の方法により行った。
(1)起泡性
2%水溶液400mlを25℃、撹拌数4300rpmでミキサー撹拌し、1分間撹拌後の液量(ml)で評価した。
◎:2000ml以上
〇:1500〜2000ml
△:1000〜1500ml
×:1000ml以下
(2)外観
試作24時間後、常温における外観を評価
〇:透明
△:半透明
×:不透明
(3)高温安定性(色調)
高温安定性は、60℃に4週間保存した後、褐変の程度を目視で観察した。
○:ほとんど褐変なし
△:やや褐変
×:褐変
(4)離漿率
ゲルを一辺約2cmの立方体に切断し、スクリュー管に密閉する。
所定温度のインキュベーターにて一週間放置後、固体ゲルを取り出し、その重量変化から離漿率を算出。
〇:2%以下
○△:2〜5%
△:5〜10%
×:10%以上
(5)ゲル硬度
試作24時間後、常温においてレオメーター(8φ)にて測定した。
(6)製造性
溶融状態(80℃)で、B型粘度計(No.3 12rpm)で測定
◎:500mPa.s以下
〇:500〜1000mPa.s
△:1000〜1500mPa.s
×:1500mPa.s以上
(7)肌へのマイルド感
肌へのマイルド感は、スティンギング刺激の低さで評価した。
すなわち、ゲル状洗浄料を、濡らした顔に直接適用することを想定し、被検試料をイオン交換水で50%水溶液に希釈する。
被検試料希釈液をつけた綿棒を、官能試験パネラーの頬上部から瞼下に塗布する。
塗布直後から8分間の間で感じたもっとも高い刺激スコアでスティンギング刺激性を評価する。
刺激スコア 感覚刺激評点の基準 評点
6 我慢できないほどの強い感覚刺激を感じる ×
5 強い感覚刺激を感じる ×
4 はっきりと感覚刺激を感じる ×
3 時々感覚刺激を感じる △
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結果を表1及び表2に示す。
前記表1,2より明らかなように、ネイティブ型ジェランガム及び脱アシル型ジェランガムともに、濃度依存的に優れた離漿抑制作用を発揮した。
特に脱アシル型ジェランガムは、形成されたゲルの透明性が高く、透明ゲル状洗浄剤を得る上では好ましいものであった。
次に本発明者らは、洗浄成分を加えた場合の評価を行った。
結果を次の表3〜6に示す。
前記表3の試験例3−1と試験例3−5を比較すると、脂肪酸石鹸を洗浄成分として用いた試験例3−5では起泡性が不十分であり、これに対し試験例3−1では洗浄成分としてポリオキシエチレンアルキルエーテルカルボン酸塩を用いることにより起泡性の大幅な改善が認められた。
しかしながら、タマリンドガムにより形成されたゲルの離漿抑制という観点からは、脱アシル型ジェランガムのみでは不十分であることが理解される。
この点は、表1,2に示した結果では、ジェランガムが単独で、タマリンドガムが形成したゲルの離漿抑制効果を示したのと対照的であり、洗浄成分による離漿促進作用が推測される。
一方、表4〜5を参照すると、試験例4−1,5−1,6−1の結果よりカチオン化キサンタンガム単独の離漿抑制効果が確認された。
さらに、カチオン化キサンタンガムの存在を前提に、ジェランガムの離漿抑制増強効果が確認された。
以上の結果より、タマリンドガムによりゲル化された洗浄剤の洗浄成分として、ポリオキシエチレンアルキルエーテルカルボン酸を用いることにより、起泡性の大幅な向上とともに、pHを7.5以下に抑制することが可能となり、肌に対する感触もマイルドになる。
結果を次の表7に示す。
表7より明らかなように、中和剤として水酸化ナトリウム、水酸化カリウム、トロメタミン(2−アミノ−2−ヒドロキシメチル−1,3−プロパンジオール)等の有機アミンを用いた場合にも、前記同様に優れた効果が発揮される。
しかも、中和剤の添加量は理論中和量未満であっても、60〜90%程度であれば、その効果を発揮することが明らかとなった。
また、表8に示すように、以上のような本発明の特性は、ポリオキシエチレンアルキルエーテルカルボン酸に共通してみられるものであることが明らかとなった。
結果を表9に示す。
表9より明らかなように、脂肪酸石鹸を用いた場合にはpHが高く、特にラウリン酸を主脂肪酸として用いた試験例9−2はスティンギング刺激が高い傾向が認められた。
しかしながら、ポリオキシエチレンアルキルエーテルカルボン酸を用いた場合(試験例9−1)には、pHを7.5以下に抑えつつ十分な起泡性を得ることができ、しかもスティンギング刺激も低いことが理解できる。また基剤としての色調安定性が良好であるため、
様々の色調に着色しても変色することがない。
さらに表10に示すように、中和剤としてトロメタミンを用い、また他のアニオン界面活性剤としてラウロイルメチルアラニンナトリウムを用いた場合にも、刺激性、起泡性を含め高い機能を有していた。
Claims (3)
- ポリオキシエチレンアルキルエーテルカルボン酸塩2〜11質量%と、
キシログルカン0.5〜3質量%と、
カチオン化キサンタンガム0.2〜3質量%と、を含み、
1%水溶液のpHが7.5以下であり、
ポリオキシエチレンアルキルエーテルカルボン酸塩の中和率は60〜90%である
ことを特徴とするゲル状洗浄剤。 - 請求項1記載の洗浄剤において、さらに脱アシル型ジェランガム0.01〜0.5質量%含むことを特徴とする透明ゲル状洗浄剤。
- 請求項1又は2記載の洗浄剤において、ポリオキシエチレンアルキルエーテルカルボン酸塩は、POE(3〜5)ラウリルエーテルカルボン酸であることを特徴とするゲル状洗浄剤。
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