JP2009536231A - 顔料混合物ならびに化粧品および食品および医薬品分野におけるその使用 - Google Patents
顔料混合物ならびに化粧品および食品および医薬品分野におけるその使用 Download PDFInfo
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- JP2009536231A JP2009536231A JP2009508248A JP2009508248A JP2009536231A JP 2009536231 A JP2009536231 A JP 2009536231A JP 2009508248 A JP2009508248 A JP 2009508248A JP 2009508248 A JP2009508248 A JP 2009508248A JP 2009536231 A JP2009536231 A JP 2009536231A
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- 235000019871 vegetable fat Nutrition 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 235000019155 vitamin A Nutrition 0.000 description 1
- 239000011719 vitamin A Substances 0.000 description 1
- 235000019154 vitamin C Nutrition 0.000 description 1
- 239000011718 vitamin C Substances 0.000 description 1
- 235000019165 vitamin E Nutrition 0.000 description 1
- 229940046009 vitamin E Drugs 0.000 description 1
- 239000011709 vitamin E Substances 0.000 description 1
- 150000003722 vitamin derivatives Chemical class 0.000 description 1
- 239000007762 w/o emulsion Substances 0.000 description 1
- 239000010497 wheat germ oil Substances 0.000 description 1
- 235000013618 yogurt Nutrition 0.000 description 1
- 229910001928 zirconium oxide Inorganic materials 0.000 description 1
- 229910006540 α-FeOOH Inorganic materials 0.000 description 1
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Abstract
Description
成分Aは
(A)モル比で1:0.5〜1:2.0のTiO2とFe2O3の混合物、ならびに場合により、層(A)を基準として<20重量%の量の1以上の金属酸化物からなる高屈折率コーティングと、
(B)n<1.8の屈折率を有する無色コーティングと、
(C)n>1.8の屈折率を有する無色コーティングと、
(D)n>1.8の屈折率を有する吸収性コーティングと、場合により、
(E)外側保護層と
を含む層配列を有する多層コートのフレーク状基材に基づくエフェクト顔料を含み、
成分Bは、無機顔料、有機顔料、色素、着色性天然果実、および/または植物抽出物の群から選択される着色剤、および/またはフレーク状、針状、球状、もしくは不規則形状の粒子からなる添加剤を含む。
基材+Fe2O3/TiO2+SiO2+TiO2+Fe2O3/TiO2、
基材+Fe2O3/TiO2+SiO2+TiO2+Fe2O3、または
基材+Fe2O3/TiO2+SiO2+TiO2+SiO2+Fe2O3/TiO2
層(A)〜(D)または(A)〜(E)は好ましくは基材表面に直接塗布される。すなわち、層(A)は基材表面上に直接設けられる。
基材+(IL)TiO2+Fe2O3/TiO2+SiO2+TiO2+Fe2O3/TiO2、または
基材+(IL)TiO2+Fe2O3/TiO2+SiO2+TiO2+Fe2O3
を含む層構造が特に好ましい。
成分Bは好ましくはコーティングされたまたはコーティングされていないSiO2ビーズを含む。1以上の金属酸化物でコーティングされたSiO2ビーズが、例えば欧州特許第0803550A2号に開示されている。
本発明による顔料混合物は、装飾用および手入れ用化粧品の両方に好都合に利用することができる。成分Aの多層顔料の使用濃度および成分B(特に、天然または合成由来の、有機および無機の有色顔料および色素、例えば酸化クロム、ウルトラマリン、球状SiO2、またはTiO2顔料など)との混合比は、塗布媒体および得ようとする効果によって決まる。
10〜60μmの粒径を有する100gの雲母を、2Lの脱塩水中で75℃に加熱する。この温度に達したら、157.5gのTiCl4(30重量%のTiCl4)、236.6gのFeCl3溶液(11.7%のFe)、5.9gのAlCl3×6H2O、および60gの脱塩水の混合溶液を、強く撹拌しながらゆっくりと量り入れる。32%水酸化ナトリウム溶液を用いてpHをpH2.6で一定に保つ。この溶液を加えたら、混合物をさらに約15分間撹拌する。続いて、32%水酸化ナトリウム溶液を用いてpHをpH=7.5まで上昇させ、431gのナトリウム水ガラス溶液(13.5%のSiO2)をこのpHでゆっくりと量り入れる。次いで10%塩酸を用いてpHを2.0まで低下させ、混合物をさらに15分間撹拌し、393gのTiCl4溶液(370g TiCl4/L)を量り入れる。この添加の間、32%水酸化ナトリウム溶液を用いてpHを一定に保つ。続いて32%水酸化ナトリウム溶液を用いてpHを2.9まで上昇させ、34gのFeCl3×6H2Oおよび49gの脱塩水からなる溶液をゆっくりと量り入れる。32%水酸化ナトリウム溶液を用いてpHをpH=2.9で一定に保つ。この溶液を添加したら、混合物をさらに約15分間撹拌する。続いて32%水酸化ナトリウム溶液を用いてpHをpH=5.0まで上昇させ、混合物をさらに15分間撹拌する。
(Phyma 22.5°/22.5°、黒色バックグラウンド)
L=77.7、a=1.4、b=32.2
実施例2
10〜60μmの粒径を有する100gの雲母を、2Lの脱塩水中で75℃に加熱する。この温度に達したら、215gのFeCl3×6H2O(11.7%のFe)、144gのTiCl4溶液(30重量%のTiCl4)、5.4gのAlCl3×6H2O、および50gの脱塩水の混合溶液を、強く撹拌しながらゆっくりと量り入れる。32%水酸化ナトリウム溶液を用いてpHをpH2.6で一定に保つ。この溶液を加えたら、混合物をさらに約15分間撹拌する。続いて、32%水酸化ナトリウム溶液を用いてpHをpH=7.5まで上昇させ、394gのナトリウム水ガラス溶液(13.5%のSiO2)をこのpHでゆっくりと量り入れる。次いで10%塩酸を用いてpHを2.0まで低下させる。混合物をさらに15分間撹拌し、次いで314gのTiCl4溶液(370g TiCl4/L)を量り入れる。この添加の間、32%水酸化ナトリウム溶液を用いてpHを一定に保つ。続いて32%水酸化ナトリウム溶液を用いてpHを2.9まで上昇させ、86gのFeCl3×6H2O溶液(11.7%のFe)および50gの脱塩水からなる溶液をゆっくりと量り入れる。32%水酸化ナトリウム溶液を用いてpHをpH=2.9で一定に保つ。この溶液を添加したら、混合物をさらに約15分間撹拌する。続いて32%水酸化ナトリウム溶液を用いてpHをpH=5.0まで上昇させ、混合物をさらに15分間撹拌する。
(Phyma 22.5°/22.5°、黒色バックグラウンド)
L=80.0、a=−0.9、b=34.0
実施例3
10〜60μmの粒径を有する100gの雲母を、2Lの脱塩水中で75℃に加熱する。この温度に達したら、215gのFeCl3×6H2O溶液(11.7%のFe)、144gのTiCl4溶液(30重量%のTiCl4)、および5.4gのAlCl3×6H2Oの50g脱塩水中混合溶液を、強く撹拌しながらゆっくりと量り入れる。32%水酸化ナトリウム溶液を用いてpHをpH2.6で一定に保つ。この溶液を加えたら、混合物をさらに約15分間撹拌する。続いて、32%水酸化ナトリウム溶液を用いてpHをpH=7.5まで上昇させ、394gのナトリウム水ガラス溶液(13.5%のSiO2)をこのpHでゆっくりと量り入れる。次いで10%塩酸を用いてpHを2.0まで低下させ、混合物をさらに15分間撹拌し、235gのTiCl4溶液(370gのTiCl4/L)を量り入れる。この添加の間、32%水酸化ナトリウム溶液を用いてpHを一定に保つ。続いて22gのナトリウム水ガラス溶液(13.5%のSiO2)をpH2.0でゆっくりと量り入れ、混合物をさらに15分間撹拌する。次いで32%水酸化ナトリウム溶液を用いてpHを2.6まで上昇させ、混合物をさらに15分間撹拌し、116gのFeCl3×6H2O(11.7%のFe)、78gのTiCl4溶液(30重量%のTiCl4)、および2.5gのAlCl3×6H2O、および30gの脱塩水からなる混合溶液をゆっくりと量り入れる。32%水酸化ナトリウム溶液を用いてpHをpH=2.6で一定に保つ。この溶液を添加したら、混合物をさらに約15分間撹拌する。続いて32%水酸化ナトリウム溶液を用いてpHをpH=5.0まで上昇させ、混合物をさらに15分間撹拌する。
(Phyma 22.5°/22.5°、黒色バックグラウンド)
L=75.0、a=−1.2、b=28.3
実施例4
10〜60μmの粒径を有する100gの雲母を、2Lの脱塩水中で75℃に加熱する。この温度に達したら、215gのFeCl3×6H2O溶液(11.7%のFe)、144gのTiCl4溶液(30重量%のTiCl4)、および5.4gのAlCl3×6H2O、および50gの脱塩水の混合溶液を、強く撹拌しながらゆっくりと量り入れる。32%水酸化ナトリウム溶液を用いてpHをpH2.6で一定に保つ。この溶液を加えたら、混合物をさらに約15分間撹拌する。続いて、32%水酸化ナトリウム溶液を用いてpHをpH=7.5まで上昇させ、394gのナトリウム水ガラス溶液(13.5%のSiO2)をこのpHでゆっくりと量り入れる。次いで10%塩酸を用いてpHを2.0まで低下させ、混合物をさらに15分間撹拌し、3.0gのSnCl4×5H2Oおよび10mLの塩酸(37%のHCl)の100mL脱イオン水中溶液をこのpHで加える。次いで10%塩酸を用いてpHを1.8まで低下させ、混合物をさらに15分間撹拌し、235gのTiCl4溶液(370gのTiCl4/L)を量り入れる。この添加の間、32%水酸化ナトリウム溶液を用いてpHを一定に保つ。次いで32%水酸化ナトリウム溶液を用いてpHを2.6まで上昇させ、混合物をさらに15分間撹拌し、116gのFeCl3×6H2O溶液(11.7%のFe)、78gのTiCl4溶液(30重量%のTiCl4)、および2.5gのAlCl3×6H2O、および30gの脱塩水の混合溶液をゆっくりと量り入れる。32%水酸化ナトリウム溶液を用いてpHをpH=2.6で一定に保つ。金属塩溶液を加えた後、混合物をさらに約15分間撹拌する。続いて32%水酸化ナトリウム溶液を用いてpHをpH=5.0まで上昇させ、混合物をさらに15分間撹拌する。
(Phyma 22.5°/22.5°、黒色バックグラウンド)L=79.0、
a=−0.9、b=31.7
を有する強い光沢性の金色顔料を得る。
使用実施例
実施例1A:入浴ジェル
相A:反応器へ水を導入し、顔料を混ぜ入れる。Keltrol CG−SFTを撹拌しながらゆっくり散らし入れ、完全に溶解してしまうまで撹拌する(均質化しない)。相Bの成分を相Aへ個別に加える。クエン酸一水和物を水中に溶解し、バッチへ加え、すべてが均質に分布するまで撹拌する。クエン酸の添加によりpHを6.0〜6.5に調整する(必要であれば)。
供給元
(1)メルク社/Rona(登録商標)
(2)C.P.Kelco
(3)Cognis GmbH
(4)Drom
(5)BASF AG
(6)Symrise
実施例2A:アイシャドー
相Aの成分を合わせ、あらかじめ混合する。続いて溶融した相Bを粉末混合物へ撹拌しながら滴下して加える。大直径の粉末用パンに粉末を導入し、80barで圧縮する。
供給元
(1)メルク社/Rona(登録商標)
(2)Suedstaerke GmbH
(3)Cognis GmbH
(4)H.Erhard Wagner GmbH
(5)Symrise
実施例3A:デイクリーム(O/W)
相Bを溶液が透明になるまで温める。Veegumを相Aの水中に分散させ、残りの原料を加え、80℃まで加熱し、相Bを加える。相A/Bを均質化する。撹拌しながら40℃まで冷却し、相Cを加える。室温まで冷却し、pH6.0に調整する。
供給元
(1)メルク社/Rona(登録商標)
(2)Vanderbilt
(3)Uniqema
(4)Cognis GmbH
(5)Sasol Germany GmbH
(6)H. Erhard Wagner GmbH
(7)Fragrance Resources
(8)Dow Corning
(9)Schulke & Mayr GmbH
実施例4A:スパークリングボディークリーム(O/W)
真珠光沢顔料を相Aの水中に分散させる。必要により、粘度を低下させるために数滴のクエン酸を用いて酸性化する。撹拌しながらCarbopolを散らし入れる。完全に溶解したら、あらかじめ溶解させた相Bをゆっくりとかき混ぜ入れる。相A/Bおよび相Cを80℃まで加熱し、相Cを相A/Bへかき混ぜ入れ、相Dと共に均質化し、中和し、再び均質化し、撹拌しながら冷却する。Germall 115を相Eの水中に40℃で溶解させ、撹拌しながら加える。次いで香油を加え、撹拌しながら室温まで冷却する。
供給元
(1)メルク社/Rona(登録商標)
(2)Noveon
(3)Cognis GmbH
(4)Clariant GmbH
(5)Nipa Laboratorien GmbH
(6)ISP Global Technologies
(7)Drom
実施例5A:クリーム状アイシャドー
相Bをすべて溶融してしまうまで約80℃に加熱し、65℃に冷却する。次いで相Aの真珠光沢顔料、Micronasphere、および粉末化した酸化クロムを加える。このアイシャドーを65℃で容器へ移す。
供給元
(1)メルク社/Rona(登録商標)
(2)Les Colorants Wackherr
(3)Croda GmbH
(4)Sasol Germany GmbH
(5)ISP Global Technologies
実施例6A:整髪ジェル
真珠光沢顔料を相Aの水中に分散させ、撹拌しながらCarbopalを散らし入れる。完全に溶解したら、あらかじめ溶解させた相Bをかき混ぜ入れる。
供給元
(1)メルク社/Rona(登録商標)
(2)Noveon
(3)BASF AG
(4)ISP Global Technologies
実施例7A:シャンプー
相Aにおいて、顔料を水中にかき混ぜ入れる。粘度を低下させるために数滴のクエン酸(10%)を用いて酸性化させ、撹拌しながらCarbopolをゆっくりと散らし入れる。完全に溶解したら、相Bをゆっくりと加える。次いで相Cの成分を順次加える。pHを6.0〜6.5に調整する。
供給元
(1)メルク社/Rona(登録商標)
(2)Noveon
(3)Cognis GmbH
(4)Fragrance Resources
実施例8A:シマリングボディパウダー
相Bのすべての成分を共に計量し、ミキサーで均一に粉砕する。続いて相Cを加え、混合を続け、次いで相Aを加え、真珠光沢顔料が均一に分布するまで短時間粉砕する。
供給元
(1)メルク社/Rona(登録商標)
(2)Cognis GmbH
(3)Sasol Germany GmbH
(4)Symrise
実施例9A:長時間持続リップグロス
相Bのすべての成分を共に計量し、80℃まで加熱し、良く撹拌する。相Aの顔料をかき混ぜ入れ、撹拌しながらNeosilを散らし入れ、最後に香料を加える。均一な混合物を容器へ移す。
供給元
(1)メルク社/Rona(登録商標)
(2)BP Lavera Sud
(3)Desert Whale
(4)Henry Lamotte Gmbh
(5)Les Colorants Wackherr
(6)Ineos Silicas Limited
(7)Symrise
実施例10A:マニキュア
マニキュアベースと共に顔料を計量し、スパチュラを用いて手で良く混合し、続いて1000rpmで10分間撹拌する。
供給元
(1)メルク社/Rona(登録商標)
(2)Durlin/Bergerac NC
実施例11A:ボリュームマスカラ(O/W)
Dermacryl 79を別にして相Bのすべての成分を共に約85℃で溶融し、撹拌しながらDermacryl 79を加え、すべてが均一に分布するまで20分間撹拌する。相Cの成分を約85℃に加熱する。相Aの真珠光沢顔料を相Cへかき混ぜ入れる。相Cを相Bへ加え、撹拌を続け、Ultra−Turrax T25を用いて8000rpmで1分間均質化する。撹拌しながら放冷し、相Dを40℃で加える。
供給元
(1)メルク社/Rona(登録商標)
(2)National Starch&Chemical
(3)Croda GmbH
(4)Degussa−Goldschmidt AG
(5)Dow Corning
(6)Nipa Laboratorien GmbH
(7)Angus Chemie GmbH
(8)ISP Global Technologies
実施例12A:紫外線保護機能を有する薄色デイクリーム(O/W)
Keoltrol Tを別にしてすべての成分を相Bの水中に分散させる。撹拌しながらKeltrolを相Bへ散らし入れ、15分後に80℃に加熱する。相Aを75℃に加熱する。相Bをゆっくりと相Aへかき混ぜ入れ、均質化させる。撹拌しながら冷却する。
供給元
(1)メルク社/Rona(登録商標)
(2)Uniqema
(3)Seppic
(4)Dow Corning
(5)Cognis GmbH
(6)C.P.Kelco
(7)Chemag AG
(8)Schulke&Mayr GmbH
実施例13A:クリームコンディショナー
顔料を相Aの水中に分散させ、残りの原料を加える。それぞれを添加した後に撹拌し、続いて75℃に加熱する。相Bの原料を混合し、75〜80℃に加熱し、相Aへ加える。均質な分配となるまで混合する。45℃で相Cを加える。
供給元
(1)メルク社/Rona(登録商標)
(2)BASF AG
(3)Cognis GmbH
(4)ISP Global Technologies
実施例1A〜13Aの化粧品配合物は、その強い金色光沢およびその非常に良好な肌感触により特徴づけられる。
実施例14A:ハードキャラメルの製造
実施例15A:錠剤のコーティング
a)白色錠剤d=8mm、G=200mgの初期重量1kg
これは、錠剤表面の1cm2あたり1.2mgのポリマーに相当する。
薄膜コーティング溶液の調製
金色顔料を水中にかき混ぜ入れる。続いて追加の色素を加える。最後に、膜形成剤(HPMC)を懸濁液へ散らし入れる。粘度上昇のため、撹拌スピードもそれに応じて上昇させなければならない。約40〜60分後に、HPMCが完全に溶解したら、溶液を錠剤上へスプレーすることができる。
Claims (21)
- 少なくとも2つの成分AおよびBからなる顔料混合物であって、
成分Aが、
(A)モル比が1:0.5〜1:2.0のTiO2とFe2O3の混合物、ならびに場合により、層(A)を基準として<20重量%の量の1以上の金属酸化物からなる高屈折率コーティングと、
(B)n<1.8の屈折率を有する無色コーティングと、
(C)n>1.8の屈折率を有する無色コーティングと、
(D)n>1.8の屈折率を有する吸収性コーティングと、場合により、
(E)外側保護層と
を含む層配列を有する多層コートのフレーク状基材に基づく効果顔料を含み、
成分Bが、無機顔料、有機顔料、染料、着色性天然果実、および/または植物抽出物の群から選択される着色剤、および/またはフレーク状、針状、球状、もしくは不規則形状の粒子からなる増量剤を含む
ことを特徴とする顔料混合物。 - 成分Aの効果顔料が、以下の層構造、
基材+Fe2O3/TiO2+SiO2+TiO2+Fe2O3/TiO2、
基材+Fe2O3/TiO2+SiO2+TiO2+Fe2O3、または
基材+Fe2O3/TiO2+SiO2+TiO2+SiO2+Fe2O3/TiO2
を有することを特徴とする、請求項1に記載の顔料混合物。 - 成分Aのフレーク状基材がTiO2またはSiO2の層で被覆されることを特徴とする、請求項1または2に記載の顔料混合物。
- 成分Aの効果顔料が、以下の層構造、
基材+TiO2+Fe2O3/TiO2+SiO2+TiO2+Fe2O3/TiO2、または
基材+TiO2+Fe2O3/TiO2+SiO2+TiO2+Fe2O3
を有することを特徴とする、請求項1から3の一項または複数項に記載の顔料混合物。 - 成分Aの効果顔料の層(A)のTiO2対Fe2O3のモル比が1:1であることを特徴とする、請求項1から4の一項または複数項に記載の顔料混合物。
- 成分Aの効果顔料の層(D)のTiO2対Fe2O3のモル比が1:1であることを特徴とする、請求項1から5の一項または複数項に記載の顔料混合物。
- 成分Aの効果顔料の層(A)が、疑似板チタン石、または疑似板チタン石とTiO2もしくは疑似板チタン石とFe2O3の混合物の層であることを特徴とする、請求項1から6の一項または複数項に記載の顔料混合物。
- 成分Aの効果顔料の層(D)が、疑似板チタン石、または疑似板チタン石とTiO2もしくは疑似板チタン石とFe2O3の混合物の層であることを特徴とする、請求項1から7の一項または複数項に記載の顔料混合物。
- 成分Aの効果顔料の層(A)および(D)がそれぞれ、疑似板チタン石、または疑似板チタン石とTiO2もしくは疑似板チタン石とFe2O3の混合物の層であることを特徴とする、請求項1から8の一項または複数項に記載の顔料混合物。
- 成分Bの着色剤が、成分Aとは異なる真珠光沢顔料、多層顔料、および/または干渉顔料、あるいはそれらの混合物であることを特徴とする、請求項1から9の一項または複数項に記載の顔料混合物。
- 成分Aおよび成分Bが混合比99:1〜50:50で混合されることを特徴とする、請求項1から10の一項または複数項に記載の顔料混合物。
- 成分Aおよび成分Bが混合比99:1〜1:99で混合され、成分Bが増量剤であることを特徴とする、請求項1から10の一項または複数項に記載の顔料混合物。
- 層配列(IL)、(A)〜(D)、または(IL)(A)〜(E)
(IL)TiO2の高屈折率コーティング、
(A)モル比が1:0.5〜1:2.0のTiO2とFe2O3の混合物、ならびに場合により、層(A)を基準として<20重量%の量の1以上の金属酸化物からなる高屈折率コーティング、
(B)n<1.8の屈折率を有する無色コーティング、
(C)n>1.8の屈折率を有する無色コーティング、
(D)n>1.8の屈折率を有する吸収性コーティング、および場合により、
(E)外側保護層
を有することを特徴とする、多層コートのフレーク状基材に基づく効果顔料。 - 以下の層構造、
基材+TiO2+Fe2O3/TiO2+SiO2+TiO2+Fe2O3/TiO2、または
基材+TiO2+Fe2O3/TiO2+SiO2+TiO2+Fe2O3
を有することを特徴とする、請求項13に記載の効果顔料。 - Fe2O3とTiO2の混合物が、疑似板チタン石、または疑似板チタン石とTiO2もしくは疑似板チタン石とFe2O3の混合物であることを特徴とする、請求項13または14に記載の効果顔料。
- 塗料、コーティング、印刷用インク、プラスチック、化粧品配合物、ならびに食品および医薬製品における、請求項13から15の一項または複数項に記載の効果顔料の使用。
- 化粧品配合物ならびに食品および医薬製品における、請求項1から12の一項または複数項に記載の顔料混合物の使用。
- 顔料混合物が芳香物質および/または甘味料と組み合わせて使用されることを特徴とする、食品および医薬製品における、請求項1から12の一項または複数項に記載の顔料混合物の使用。
- 請求項1から12の一項または複数項に記載の顔料混合物を含む配合物。
- 請求項1から12の一項または複数項に記載の顔料混合物を、配合物全体を基準として0.01〜99重量%の量で含む配合物。
- 水、ポリオール、極性または非極性の油、脂肪、ワックス、膜形成剤、ポリマー、コポリマー、界面活性剤、遊離基捕捉剤、酸化防止剤、安定化剤、香気増強剤、シリコーン油、乳化剤、溶媒、保存料、増粘剤、レオロジー添加剤、香料、紫外線吸収剤、表面活性補助剤、および/または化粧品活性化合物をさらに含むことを特徴とする、請求項1から12の一項または複数項に記載の顔料混合物を含む、請求項19または20に記載の配合物。
Applications Claiming Priority (2)
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DE102006021784A DE102006021784A1 (de) | 2006-05-09 | 2006-05-09 | Effektpigmente und deren Verwendung in der Kosmetik und im Lebensmittel- und Pharmabereich |
PCT/EP2007/004097 WO2007128576A2 (de) | 2006-05-09 | 2007-05-09 | Pigmentgemisch und dessen verwendung in der kosmetik und im lebensmittel- und pharmabereich |
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JP2013240893A Pending JP2014077137A (ja) | 2006-05-09 | 2013-11-21 | 顔料混合物ならびに化粧品および食品および医薬品分野におけるその使用 |
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US (3) | US20090246294A1 (ja) |
EP (1) | EP2016136A2 (ja) |
JP (2) | JP2009536231A (ja) |
KR (2) | KR20140051400A (ja) |
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JP2015096606A (ja) * | 2007-12-17 | 2015-05-21 | メルク パテント ゲゼルシャフト ミット ベシュレンクテル ハフツングMerck Patent Gesellschaft mit beschraenkter Haftung | フィラー顔料 |
JP2015131937A (ja) * | 2013-12-11 | 2015-07-23 | 株式会社Adeka | 着色性組成物 |
JP2020510118A (ja) * | 2017-04-21 | 2020-04-02 | Cqv株式会社Cqv Co., Ltd. | 複合白色顔料 |
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JP2021080235A (ja) * | 2019-11-22 | 2021-05-27 | 株式会社ノエビア | 皮膚外用剤 |
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Publication number | Publication date |
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JP2014077137A (ja) | 2014-05-01 |
WO2007128576A2 (de) | 2007-11-15 |
KR20140051400A (ko) | 2014-04-30 |
US20130108569A1 (en) | 2013-05-02 |
CN101460572A (zh) | 2009-06-17 |
US20090246294A1 (en) | 2009-10-01 |
EP2016136A2 (de) | 2009-01-21 |
US20160230012A1 (en) | 2016-08-11 |
DE102006021784A1 (de) | 2007-11-15 |
WO2007128576A3 (de) | 2008-11-20 |
KR20090009961A (ko) | 2009-01-23 |
DE112007001008A5 (de) | 2009-04-23 |
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