JP2014504318A - 過酸化水素または過酸化水素放出性物質を含む組成物 - Google Patents
過酸化水素または過酸化水素放出性物質を含む組成物 Download PDFInfo
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- C07D213/89—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members with hetero atoms directly attached to the ring nitrogen atom
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- D06L4/10—Bleaching fibres, filaments, threads, yarns, fabrics, feathers or made-up fibrous goods; Bleaching leather or furs using agents which develop oxygen
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Abstract
b)水、
d)ヒドロキシピリドン類及びそれの塩からなる群から選択される一種またはそれ以上の物質、
を含む組成物であって、増粘性を有するポリマーを含まないことを特徴とする組成物が開示される。該組成物は、特にその有利な貯蔵安定性を特色とする。
Description
a)過酸化水素及び過酸化水素放出性物質からなる群から選択される一種またはそれ以上の物質、
b)水、
d)ヒドロキシピロリドン類及びその塩からなる群から選択される一種またはそれ以上の物質を含む組成物であって、増粘性を有するポリマーを含まないことを特徴とする前記組成物である。
スピンドルセットRVからのスピンドルが使用される。これらの測定条件下に、最大500mPa・sの粘度にはスピンドル1が、最大1000mPa・sの粘度にはスピンドル2が、そして最大5000mPa・sの粘度にはスピンドル3が選択される。
例1:
Solvay社の過酸化水素溶液(水中35重量%)またはMerck社の過酸化水素溶液(水中35重量%)を、完全脱塩水を用いて約6.0重量%の過酸化水素含有率に希釈し、そして水酸化ナトリウム溶液(20重量%)を用いて9.0のpH値に調節した。更に別の溶液に、それぞれ8ppmの4−メチル−6−(2,4,4−トリメチルペンチル)−1−ヒドロキシ−2−ピリドン(添加剤A、プロピレングリコール中に溶解)を添加剤として加えた。これらの溶液を、室温(20℃)及び40℃で1週間貯蔵し、そして貯蔵前と貯蔵後の過酸化水素含有率を測定した(表1参照)。
Solvay社の過酸化水素溶液(水中35重量%)またはMerck社の過酸化水素溶液(水中35重量%)、C14−17アルキル第二スルホン酸ナトリウムの溶液(Hostapur(登録商標)SAS30)及び完全脱塩水を、過酸化水素含有率が約6.0重量%に及びC14−17アルキル第二スルホン酸ナトリウムの含有率が5.0重量%となるように混合した。その後、水酸化ナトリウム溶液(20重量%)を用いてpH値を9.0に調節した。更に別の溶液に、それぞれ7ppmの4−メチル−6−(2,4,4−トリメチルペンチル)−1−ヒドロキシ−2−ピリドン(添加剤A、プロピレングリコール中に溶解)を添加剤として加えた。これらの溶液を、室温及び40℃で1週間貯蔵し、そして貯蔵前と貯蔵後の過酸化水素含有率を測定した(表2参照)。
4−メチル−6−(2,4,4−トリメチルペンチル)−1−ヒドロキシ−2−ピリドンモノエタノールアミン塩(Octopirox(登録商標))をプロピレングリコール中に溶解する。界面活性剤を水中に溶解し、過酸化水素溶液及び前記プロピレングリコール溶液を導入し、そしてホモジナイズする。生成物をpH=4に調節する。
4−メチル−6−(シクロヘキシル)−1−ヒドロキシ−2−ピリドンをプロピレングリコール中に溶解する。界面活性剤を水中に溶解し、過酸化水素溶液及び前記プロピレングリコール溶液を導入し、そしてホモジナイズする。生成物をpH=7に調節する。
4−メチル−6−(2,4,4−トリメチルペンチル)−1−ヒドロキシ−2−ピリドンをプロピレングリコール中に溶解する。界面活性剤を水中に溶解し、過酸化水素溶液及び前記プロピレングリコール溶液を導入し、そしてホモジナイズする。生成物をpH=4.7に調節する。
Claims (13)
- a)過酸化水素及び過酸化水素放出性物質からなる群から選択される一種またはそれ以上の物質、
b)水、
d)ヒドロキシピリドン類及びそれの塩からなる群から選択される一種またはそれ以上の物質、
を含む組成物であって、増粘性を有するポリマーを含まないことを特徴とする前記組成物。 - 成分a)の一種またはそれ以上の物質が、過酸化水素、過酸化尿素、過ホウ酸塩、過硫酸塩及びこれらの混合物からなる群から選択されることを特徴とする、請求項1に記載の組成物。
- 成分a)の物質が過酸化水素であり、かつ過酸化水素が、組成物の総重量を基準にして0.5〜20重量%の量で組成物中に含まれることを特徴とする、請求項1または2に記載の組成物。
- 成分d)の一種またはそれ以上の化合物が、酸の形で、またはそれのアルカリ金属塩、アルカリ土類金属塩もしくはアミン塩の形で、またはポリマー性対イオンとのそれの塩の形で存在することを特徴とする、請求項1〜4の一つまたはそれ以上に記載の組成物。
- 式(I)の一種またはそれ以上の化合物またはそれの塩において、R1がメチルであり、かつR2がシクロヘキシルまたは2,4,4−トリメチルペンチルであることを特徴とする、請求項4または5に記載の組成物。
- 成分d)の一種またはそれ以上の物質を、組成物の総重量を基準にして0.1ppm〜2重量%の量で含むことを特徴とする、請求項1〜6の一つまたはそれ以上に記載の組成物。
- 成分d)の一種またはそれ以上の物質を、組成物の総重量を基準にして0.5〜100ppmの量で含むことを特徴とする、請求項7に記載の組成物。
- 2〜11のpH値を有することを特徴とする、請求項1〜8の一つまたはそれ以上に記載の組成物。
- 7〜11のpH値を有することを特徴とする、請求項9に記載の組成物。
- 毛髪の漂白及び/または着色用の組成物であるかあるいはパーマネントウェーブ用調合物であることを特徴とする、請求項1〜10の一つまたはそれ以上に記載の組成物。
- 酸化的洗浄剤調合物であることを特徴とする、請求項1〜10の一つまたはそれ以上に記載の組成物。
- 繊維またはテクスタイル材料の酸化的漂白のための組成物であることを特徴とする、請求項1〜10の一つまたはそれ以上に記載の組成物。
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Application Number | Priority Date | Filing Date | Title |
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DE102010054866A DE102010054866A1 (de) | 2010-12-17 | 2010-12-17 | Zusammensetzungen enthaltend Wasserstoffperoxid oder Wasserstoffperoxid freisetzende Substanzen |
DE102010054866.9 | 2010-12-17 | ||
PCT/EP2011/006277 WO2012079739A1 (de) | 2010-12-17 | 2011-12-13 | Zusammensetzungen enthaltend wasserstoffperoxid oder wasserstoffperoxid freisetzende substanzen |
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JP2014504318A true JP2014504318A (ja) | 2014-02-20 |
JP5889329B2 JP5889329B2 (ja) | 2016-03-22 |
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JP2013543571A Expired - Fee Related JP5889329B2 (ja) | 2010-12-17 | 2011-12-13 | 過酸化水素または過酸化水素放出性物質を含む組成物 |
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US (1) | US9592185B2 (ja) |
EP (1) | EP2651816B1 (ja) |
JP (1) | JP5889329B2 (ja) |
CN (2) | CN106520406A (ja) |
BR (1) | BR112013014563A2 (ja) |
DE (1) | DE102010054866A1 (ja) |
ES (1) | ES2533708T3 (ja) |
MX (1) | MX2013006889A (ja) |
WO (1) | WO2012079739A1 (ja) |
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CN103124690B (zh) | 2010-07-27 | 2015-11-25 | 科莱恩金融(Bvi)有限公司 | 含有过氧化氢或释放过氧化氢的物质的组合物 |
BR112013001953A2 (pt) | 2010-07-27 | 2018-05-15 | Clariant Finance Bvi Ltd | uso de hidroxipiridonas ou sais dos mesmos para a estabilização de peróxido de hidrogênio ou substâncias doadoras de peróxido de hidrogênio |
DE102011077046A1 (de) * | 2011-06-07 | 2012-12-13 | Beiersdorf Ag | Wirkstoffkombinationen aus å-Polylysin (Epsilon-Polylysin) und Pirocton Olamin |
CA2934519A1 (en) * | 2013-12-18 | 2015-06-25 | Arkema Inc. | Stable liquid compositions containing enzymes and peroxides |
DE102015219009A1 (de) | 2015-10-01 | 2017-04-06 | Beiersdorf Ag | Sonnenschutzmittel mit reduzierter Textilverfleckung durch Diethylamino Hydroxybenzoyl Hexyl Benzoate |
DE102015219006A1 (de) | 2015-10-01 | 2017-04-20 | Beiersdorf Ag | Sonnenschutzmittel mit reduzierter Textilverfleckung durch Bis-Ethylhexyloxyphenol Methoxyphenyl Triazine |
DE102015219008A1 (de) | 2015-10-01 | 2017-04-06 | Beiersdorf Ag | Sonnenschutzmittel mit reduzierter Textilverfleckung durch 4-(tert.-Butyl)-4'-methoxydibenzoylmethan |
DE102015219592A1 (de) | 2015-10-09 | 2017-04-13 | Beiersdorf Aktiengesellschaft | Sonnenschutzmittel mit stark reduzierter Textilverfleckung durch Bis-Ethylhexyloxyphenol Methoxyphenyl Triazine |
DE102015219591A1 (de) | 2015-10-09 | 2017-04-13 | Beiersdorf Aktiengesellschaft | Sonnenschutzmittel mit stark reduierter Textilverfleckung durch 4-(tert.-Butyl)-4 - methoxydibenzoylmethan |
US10858249B2 (en) * | 2016-11-21 | 2020-12-08 | Diversey, Inc. | Peroxide stabilizers |
CN107374995A (zh) * | 2017-06-12 | 2017-11-24 | 许昌学院 | 一种人发漂白试剂及其制备与使用方法 |
DE102019210907A1 (de) | 2019-07-23 | 2021-01-28 | Henkel Ag & Co. Kgaa | Mittel zur oxidativen Aufhellung und Blondierung der Haare |
ES1258595Y (es) * | 2020-09-28 | 2021-03-12 | Laboratorios Vinfer S A | Formulacion de limpieza acida |
ES1258594Y (es) * | 2020-09-28 | 2021-03-12 | Laboratorios Vinfer S A | Formulacion de limpieza alcalina |
WO2023213523A1 (en) * | 2022-05-06 | 2023-11-09 | Unilever Ip Holdings B.V. | Detergent composition |
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- 2010-12-17 DE DE102010054866A patent/DE102010054866A1/de not_active Withdrawn
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- 2011-12-13 EP EP11796632.5A patent/EP2651816B1/de active Active
- 2011-12-13 JP JP2013543571A patent/JP5889329B2/ja not_active Expired - Fee Related
- 2011-12-13 WO PCT/EP2011/006277 patent/WO2012079739A1/de active Application Filing
- 2011-12-13 ES ES11796632.5T patent/ES2533708T3/es active Active
- 2011-12-13 US US13/994,337 patent/US9592185B2/en active Active
- 2011-12-13 BR BR112013014563A patent/BR112013014563A2/pt not_active IP Right Cessation
- 2011-12-13 CN CN201610908318.9A patent/CN106520406A/zh active Pending
- 2011-12-13 CN CN201180060035.9A patent/CN103313932B/zh not_active Expired - Fee Related
- 2011-12-13 MX MX2013006889A patent/MX2013006889A/es unknown
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Also Published As
Publication number | Publication date |
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WO2012079739A1 (de) | 2012-06-21 |
CN103313932B (zh) | 2016-11-23 |
JP5889329B2 (ja) | 2016-03-22 |
ES2533708T3 (es) | 2015-04-14 |
BR112013014563A2 (pt) | 2016-09-20 |
EP2651816B1 (de) | 2015-02-25 |
CN106520406A (zh) | 2017-03-22 |
MX2013006889A (es) | 2013-07-05 |
US9592185B2 (en) | 2017-03-14 |
EP2651816A1 (de) | 2013-10-23 |
CN103313932A (zh) | 2013-09-18 |
DE102010054866A1 (de) | 2011-08-18 |
US20130272984A1 (en) | 2013-10-17 |
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