ES2617535T3 - Empleo de N-metil-N-acilglucaminas como estabilizadores en frío en disoluciones de agentes tensioactivos - Google Patents
Empleo de N-metil-N-acilglucaminas como estabilizadores en frío en disoluciones de agentes tensioactivos Download PDFInfo
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- ES2617535T3 ES2617535T3 ES13725683.0T ES13725683T ES2617535T3 ES 2617535 T3 ES2617535 T3 ES 2617535T3 ES 13725683 T ES13725683 T ES 13725683T ES 2617535 T3 ES2617535 T3 ES 2617535T3
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- surfactants
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- alkyl
- methyl
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- 239000004094 surface-active agent Substances 0.000 title claims abstract description 57
- 239000003381 stabilizer Substances 0.000 title claims abstract description 7
- -1 alkylene ether sulfates Chemical class 0.000 claims abstract description 29
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims abstract description 17
- 150000008051 alkyl sulfates Chemical class 0.000 claims abstract description 15
- 239000007864 aqueous solution Substances 0.000 claims abstract description 15
- 239000003945 anionic surfactant Substances 0.000 claims abstract description 9
- KWIUHFFTVRNATP-UHFFFAOYSA-N Betaine Natural products C[N+](C)(C)CC([O-])=O KWIUHFFTVRNATP-UHFFFAOYSA-N 0.000 claims abstract 4
- 229960003237 betaine Drugs 0.000 claims abstract 3
- 239000000203 mixture Substances 0.000 claims description 32
- 239000000049 pigment Substances 0.000 claims description 15
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 claims description 14
- 239000003755 preservative agent Substances 0.000 claims description 10
- 239000000126 substance Substances 0.000 claims description 8
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 claims description 7
- 239000002280 amphoteric surfactant Substances 0.000 claims description 6
- 239000003795 chemical substances by application Substances 0.000 claims description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 6
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- 229940043264 dodecyl sulfate Drugs 0.000 claims description 4
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 claims description 3
- 125000002091 cationic group Chemical group 0.000 claims description 3
- 239000003093 cationic surfactant Substances 0.000 claims description 3
- 229910052709 silver Inorganic materials 0.000 claims description 3
- 239000004332 silver Substances 0.000 claims description 3
- FKKAGFLIPSSCHT-UHFFFAOYSA-N 1-dodecoxydodecane;sulfuric acid Chemical compound OS(O)(=O)=O.CCCCCCCCCCCCOCCCCCCCCCCCC FKKAGFLIPSSCHT-UHFFFAOYSA-N 0.000 claims description 2
- QCDWFXQBSFUVSP-UHFFFAOYSA-N 2-phenoxyethanol Chemical compound OCCOC1=CC=CC=C1 QCDWFXQBSFUVSP-UHFFFAOYSA-N 0.000 claims description 2
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- BEFDCLMNVWHSGT-UHFFFAOYSA-N ethenylcyclopentane Chemical compound C=CC1CCCC1 BEFDCLMNVWHSGT-UHFFFAOYSA-N 0.000 claims description 2
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- 125000002947 alkylene group Chemical group 0.000 claims 1
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- 125000004432 carbon atom Chemical group C* 0.000 description 12
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- 230000002209 hydrophobic effect Effects 0.000 description 5
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- 239000002537 cosmetic Substances 0.000 description 4
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- MUCRPQTWSDXOKV-UHFFFAOYSA-N 1-[2-(2-hydroxyethoxy)ethoxy]tetradecan-2-ol Chemical compound CCCCCCCCCCCCC(O)COCCOCCO MUCRPQTWSDXOKV-UHFFFAOYSA-N 0.000 description 3
- HIXDQWDOVZUNNA-UHFFFAOYSA-N 2-(3,4-dimethoxyphenyl)-5-hydroxy-7-methoxychromen-4-one Chemical compound C=1C(OC)=CC(O)=C(C(C=2)=O)C=1OC=2C1=CC=C(OC)C(OC)=C1 HIXDQWDOVZUNNA-UHFFFAOYSA-N 0.000 description 3
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- IIZPXYDJLKNOIY-JXPKJXOSSA-N 1-palmitoyl-2-arachidonoyl-sn-glycero-3-phosphocholine Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@H](COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCC\C=C/C\C=C/C\C=C/C\C=C/CCCCC IIZPXYDJLKNOIY-JXPKJXOSSA-N 0.000 description 2
- 241000251468 Actinopterygii Species 0.000 description 2
- ZCTQGTTXIYCGGC-UHFFFAOYSA-N Benzyl salicylate Chemical compound OC1=CC=CC=C1C(=O)OCC1=CC=CC=C1 ZCTQGTTXIYCGGC-UHFFFAOYSA-N 0.000 description 2
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- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 2
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- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 2
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- 229940063953 ammonium lauryl sulfate Drugs 0.000 description 1
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- JDRSMPFHFNXQRB-IBEHDNSVSA-N decyl glucoside Chemical compound CCCCCCCCCCO[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O JDRSMPFHFNXQRB-IBEHDNSVSA-N 0.000 description 1
- SQIFACVGCPWBQZ-UHFFFAOYSA-N delta-terpineol Natural products CC(C)(O)C1CCC(=C)CC1 SQIFACVGCPWBQZ-UHFFFAOYSA-N 0.000 description 1
- 239000003599 detergent Substances 0.000 description 1
- 229940095104 dimethyl benzyl carbinyl acetate Drugs 0.000 description 1
- REZZEXDLIUJMMS-UHFFFAOYSA-M dimethyldioctadecylammonium chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCCCC[N+](C)(C)CCCCCCCCCCCCCCCCCC REZZEXDLIUJMMS-UHFFFAOYSA-M 0.000 description 1
- 238000004851 dishwashing Methods 0.000 description 1
- SMVRDGHCVNAOIN-UHFFFAOYSA-L disodium;1-dodecoxydodecane;sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O.CCCCCCCCCCCCOCCCCCCCCCCCC SMVRDGHCVNAOIN-UHFFFAOYSA-L 0.000 description 1
- 239000004664 distearyldimethylammonium chloride (DHTDMAC) Substances 0.000 description 1
- ZITKDVFRMRXIJQ-UHFFFAOYSA-N dodecane-1,2-diol Chemical compound CCCCCCCCCCC(O)CO ZITKDVFRMRXIJQ-UHFFFAOYSA-N 0.000 description 1
- 125000004185 ester group Chemical group 0.000 description 1
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- 235000019387 fatty acid methyl ester Nutrition 0.000 description 1
- 239000004872 foam stabilizing agent Substances 0.000 description 1
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- 229940113087 geraniol Drugs 0.000 description 1
- 239000008103 glucose Substances 0.000 description 1
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- 235000011187 glycerol Nutrition 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
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- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
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- 150000002499 ionone derivatives Chemical class 0.000 description 1
- DCYOBGZUOMKFPA-UHFFFAOYSA-N iron(2+);iron(3+);octadecacyanide Chemical compound [Fe+2].[Fe+2].[Fe+2].[Fe+3].[Fe+3].[Fe+3].[Fe+3].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-] DCYOBGZUOMKFPA-UHFFFAOYSA-N 0.000 description 1
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
- 239000000787 lecithin Substances 0.000 description 1
- 235000010445 lecithin Nutrition 0.000 description 1
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- SDQFDHOLCGWZPU-UHFFFAOYSA-N lilial Chemical compound O=CC(C)CC1=CC=C(C(C)(C)C)C=C1 SDQFDHOLCGWZPU-UHFFFAOYSA-N 0.000 description 1
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- 238000002844 melting Methods 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
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- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
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- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
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- RUVINXPYWBROJD-UHFFFAOYSA-N para-methoxyphenyl Natural products COC1=CC=C(C=CC)C=C1 RUVINXPYWBROJD-UHFFFAOYSA-N 0.000 description 1
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- 239000000825 pharmaceutical preparation Substances 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
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- 229920001983 poloxamer Polymers 0.000 description 1
- 229920001748 polybutylene Polymers 0.000 description 1
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- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
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Classifications
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- 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
- A61K8/42—Amides
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- A—HUMAN NECESSITIES
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- 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
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- A—HUMAN NECESSITIES
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- 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
- A61K8/442—Aminocarboxylic acids or derivatives thereof, e.g. aminocarboxylic acids containing sulfur; Salts; Esters or N-acylated derivatives thereof substituted by amido group(s)
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- A—HUMAN NECESSITIES
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- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
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- 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
- A61K8/46—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing sulfur
- A61K8/463—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing sulfur containing sulfuric acid derivatives, e.g. sodium lauryl sulfate
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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
- A61K8/46—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing sulfur
- A61K8/466—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing sulfur containing sulfonic acid derivatives; Salts
-
- 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
- A61Q19/10—Washing or bathing preparations
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q5/00—Preparations for care of the hair
- A61Q5/02—Preparations for cleaning the hair
-
- 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
- C11D1/52—Carboxylic amides, alkylolamides or imides or their condensation products with alkylene oxides
- C11D1/525—Carboxylic amides (R1-CO-NR2R3), where R1, R2 or R3 contain two or more hydroxy groups per alkyl group, e.g. R3 being a reducing sugar rest
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
- A61K2800/40—Chemical, physico-chemical or functional or structural properties of particular ingredients
- A61K2800/59—Mixtures
- A61K2800/592—Mixtures of compounds complementing their respective functions
- A61K2800/5922—At least two compounds being classified in the same subclass of A61K8/18
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
- A61K2800/40—Chemical, physico-chemical or functional or structural properties of particular ingredients
- A61K2800/59—Mixtures
- A61K2800/596—Mixtures of surface active compounds
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Epidemiology (AREA)
- Birds (AREA)
- Chemical & Material Sciences (AREA)
- Dermatology (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Cosmetics (AREA)
- Detergent Compositions (AREA)
- Emulsifying, Dispersing, Foam-Producing Or Wetting Agents (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE102012010700 | 2012-05-30 | ||
| DE102012010700 | 2012-05-30 | ||
| PCT/EP2013/061046 WO2013178670A2 (de) | 2012-05-30 | 2013-05-29 | Verwendung von n-methyl-n-acylglucaminen als kältestabilisatoren in tensidlösungen |
Publications (1)
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| ES2617535T3 true ES2617535T3 (es) | 2017-06-19 |
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| EP (1) | EP2854950B1 (en:Method) |
| JP (1) | JP6120953B2 (en:Method) |
| CN (1) | CN104394936B (en:Method) |
| BR (1) | BR112014029752A2 (en:Method) |
| ES (1) | ES2617535T3 (en:Method) |
| IN (1) | IN2014DN09938A (en:Method) |
| WO (1) | WO2013178670A2 (en:Method) |
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| Publication number | Priority date | Publication date | Assignee | Title |
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| EP2854951B1 (de) | 2012-05-30 | 2016-09-07 | Clariant International Ltd. | Zusammensetzung enthaltend aminosäuretenside, betaine und n-methyl-n-acylglucamine mit verbesserter schaumqualität und höherer viskosität |
| US10813862B2 (en) | 2012-05-30 | 2020-10-27 | Clariant International Ltd. | Use of N-methyl-N-acylglucamines as solubilizers |
| US9504636B2 (en) | 2012-05-30 | 2016-11-29 | Clariant International Ltd. | Surfactant solutions containing N-methyl-N-oleylglucamines and N-methyl-N-C12-C14-acylglucamines |
| WO2013178679A2 (de) | 2012-05-30 | 2013-12-05 | Clariant International Ltd. | N-methyl-n-acylglucamin enthaltende zusammensetzung |
| JP6442400B2 (ja) | 2012-05-30 | 2018-12-19 | クラリアント・ファイナンス・（ビーブイアイ）・リミテッド | Ｎ−メチル−ｎ−アシルグルカミンの界面活性剤溶液中における増粘剤としての使用 |
| IN2014DN09928A (en:Method) | 2012-05-30 | 2015-08-14 | Clariant Int Ltd | |
| DE102012021647A1 (de) | 2012-11-03 | 2014-05-08 | Clariant International Ltd. | Wässrige Adjuvant-Zusammensetzungen |
| ES2640385T3 (es) * | 2013-04-20 | 2017-11-02 | Clariant International Ltd. | Composición que contiene cuerpos oleaginosos, ácidos grasos, agentes tensioactivos de aminoácido y N-metil-N-acilglucaminas |
| EP3013427B1 (de) * | 2013-06-28 | 2017-08-09 | Clariant International Ltd | Verwendung von speziellen n-alkyl-n-acylglucaminen zur haarkonditionierung in haarwaschmitteln |
| ES2718665T3 (es) * | 2013-06-28 | 2019-07-03 | Clariant Int Ltd | Uso de N-alquil-N-acilglucaminas especiales en detergentes lavavajillas a mano |
| DE102013018001A1 (de) * | 2013-11-29 | 2015-06-03 | Clariant International Ltd. | Verwendung von Glucamiden zur Verbesserung der Silikondeposition |
| DE102013018000A1 (de) * | 2013-11-29 | 2015-06-03 | Clariant International Ltd. | Konditioniershampoos enthaltend anionische Tenside, Glucamide und Fettalkohole |
| DE102013225373A1 (de) * | 2013-12-10 | 2014-04-24 | Henkel Ag & Co. Kgaa | Haarbehandlungsmittel enthaltend Carbonsäure-N-alkylpolyhydroxyalkylamide |
| DE202014010354U1 (de) | 2014-03-06 | 2015-05-15 | Clariant International Ltd. | Korrosionsinhibierende Zusammensetzungen |
| DE202014010358U1 (de) * | 2014-03-06 | 2015-05-06 | Clariant International Ltd. | Verwendung von N-Methyl-N-acylglucamin als Korrosionsinhibitor |
| DE102014005771A1 (de) | 2014-04-23 | 2015-10-29 | Clariant International Ltd. | Verwendung von wässrigen driftreduzierenden Zusammensetzungen |
| DE202014008417U1 (de) | 2014-04-30 | 2014-11-24 | Clariant International Ltd. | Tensidkonzentrate zur Förderung von Bodenbefeuchtung und Pflanzenwachstum |
| DE202015008045U1 (de) | 2015-10-09 | 2015-12-09 | Clariant International Ltd. | Universelle Pigmentdispersionen auf Basis von N-Alkylglukaminen |
| DE102015219651A1 (de) | 2015-10-09 | 2017-04-13 | Clariant International Ltd. | Zusammensetzungen enthaltend Zuckeramin und Fettsäure |
| DE202016003070U1 (de) | 2016-05-09 | 2016-06-07 | Clariant International Ltd. | Stabilisatoren für Silikatfarben |
| ES2825033T3 (es) * | 2017-08-16 | 2021-05-14 | Procter & Gamble | Composición limpiadora antimicrobiana |
| US10736830B2 (en) | 2018-11-02 | 2020-08-11 | Colgate-Palmolive Company | Oral care compositions and methods for the same |
| EP3670495A1 (en) * | 2018-12-21 | 2020-06-24 | Clariant International Ltd | Glucamide-based surfactants |
| US10918584B2 (en) | 2018-12-26 | 2021-02-16 | Colgate-Palmolive Company | Oral care compositions and methods for the same |
| WO2022128781A1 (en) * | 2020-12-17 | 2022-06-23 | Unilever Ip Holdings B.V. | Cleaning composition |
| CN116583583A (zh) * | 2020-12-17 | 2023-08-11 | 联合利华知识产权控股有限公司 | 用途和清洁组合物 |
| CN114917154A (zh) * | 2021-07-29 | 2022-08-19 | 青龙高科技股份有限公司 | 一种茶油洗发水及其制备方法 |
Family Cites Families (24)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| ATE157392T1 (de) * | 1990-09-28 | 1997-09-15 | Procter & Gamble | Polyhydroxyfettsäureamide und ein oder mehrere zusätzliche nichtionische tenside enthaltende nichtionische tensidsysteme |
| US5194639A (en) * | 1990-09-28 | 1993-03-16 | The Procter & Gamble Company | Preparation of polyhydroxy fatty acid amides in the presence of solvents |
| FI931368A7 (fi) * | 1990-09-28 | 1993-04-26 | Procter & Gamble | Pesuainekoostumuksia, jotka sisältävät anionisia pinta-aktiivisia aine ita, polyhydroksirasvahappoamideja ja magnesiumia |
| JP3046071B2 (ja) * | 1990-09-28 | 2000-05-29 | ザ、プロクター、エンド、ギャンブル、カンパニー | ポリヒドロキシ脂肪酸アミド界面活性剤とアルキルエステルスルホネート界面活性剤とを含有する洗剤組成物 |
| WO1992006162A1 (en) * | 1990-09-28 | 1992-04-16 | The Procter & Gamble Company | Detergent containing alkyl sulfate and polyhydroxy fatty acid amide surfactants |
| FI941056A7 (fi) * | 1991-09-06 | 1994-05-03 | Procter & Gamble | Kalsiumia ja polyhydroksirasvahappoamidia sisältäviä pesuainekoostumuk sia |
| WO1994010273A1 (en) * | 1992-11-04 | 1994-05-11 | The Procter & Gamble Company | Detergent gels |
| US5622834A (en) * | 1993-12-01 | 1997-04-22 | Marine Polymer Technologies, Inc. | Method of isolating poly-β-1-4-N-acetylglucosamine from microalgal culture |
| BR9408437A (pt) * | 1993-12-30 | 1997-08-05 | Procter & Gamble | Xampús de alta deposição e de alta formação de espuma com sistema tensoativo suave |
| DE4416566A1 (de) * | 1994-05-11 | 1995-11-16 | Huels Chemische Werke Ag | Wäßrige viskoelastische Tensidlösungen zur Haar- und Hautreinigung |
| DE4439091A1 (de) | 1994-11-02 | 1996-05-09 | Henkel Kgaa | Oberflächenaktive Mittel |
| EP0756000A1 (en) * | 1995-07-24 | 1997-01-29 | The Procter & Gamble Company | Detergent compositions comprising specific amylase and linear alkyl benzene sulfonate surfactant |
| GB9613941D0 (en) * | 1996-07-03 | 1996-09-04 | Procter & Gamble | Cleansing compositions |
| CN1168807C (zh) * | 1997-07-21 | 2004-09-29 | 普罗格特-甘布尔公司 | 改良的烷基苯磺酸盐表面活性剂组合物 |
| MA24811A1 (fr) * | 1997-10-23 | 1999-12-31 | Procter & Gamble | Compositions de lavage contenant des variantes de proteases multisubstituees |
| US6610645B2 (en) * | 1998-03-06 | 2003-08-26 | Eugene Joseph Pancheri | Selected crystalline calcium carbonate builder for use in detergent compositions |
| US6699828B1 (en) * | 1999-06-28 | 2004-03-02 | The Procter & Gamble Company | Aqueous liquid detergent compositions comprising an effervescent system |
| EP1206519B1 (en) * | 1999-08-27 | 2005-11-30 | The Procter & Gamble Company | Stable formulation components, compositions and laundry methods employing same |
| DE19961256A1 (de) * | 1999-12-18 | 2001-06-21 | Clariant Gmbh | Kosmetische Zubereitungen |
| CA2494320C (en) * | 2002-08-13 | 2012-10-16 | Mcintyre Group, Ltd. | High concentration surfactant compositions and methods |
| US7250392B1 (en) * | 2003-03-07 | 2007-07-31 | Cognis Corporation | Surfactant blend for cleansing wipes |
| US7618801B2 (en) * | 2007-10-30 | 2009-11-17 | Danison US Inc. | Streptomyces protease |
| FR2959666B1 (fr) * | 2010-05-07 | 2012-07-20 | Oreal | Composition cosmetique moussante a base d'acide ellagique ou d'un de ses derives et d'huile essentielle. |
| IN2014DN09928A (en:Method) * | 2012-05-30 | 2015-08-14 | Clariant Int Ltd |
-
2013
- 2013-05-29 ES ES13725683.0T patent/ES2617535T3/es active Active
- 2013-05-29 WO PCT/EP2013/061046 patent/WO2013178670A2/de active Application Filing
- 2013-05-29 CN CN201380028740.XA patent/CN104394936B/zh active Active
- 2013-05-29 IN IN9938DEN2014 patent/IN2014DN09938A/en unknown
- 2013-05-29 JP JP2015514481A patent/JP6120953B2/ja active Active
- 2013-05-29 BR BR112014029752A patent/BR112014029752A2/pt not_active IP Right Cessation
- 2013-05-29 EP EP13725683.0A patent/EP2854950B1/de active Active
- 2013-05-29 US US14/402,996 patent/US20150164755A1/en not_active Abandoned
Also Published As
| Publication number | Publication date |
|---|---|
| WO2013178670A3 (de) | 2014-06-26 |
| IN2014DN09938A (en:Method) | 2015-08-14 |
| US20150164755A1 (en) | 2015-06-18 |
| JP6120953B2 (ja) | 2017-04-26 |
| WO2013178670A2 (de) | 2013-12-05 |
| CN104394936A (zh) | 2015-03-04 |
| EP2854950B1 (de) | 2016-12-14 |
| CN104394936B (zh) | 2017-08-25 |
| JP2015519451A (ja) | 2015-07-09 |
| EP2854950A2 (de) | 2015-04-08 |
| BR112014029752A2 (pt) | 2017-06-27 |
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