WO2012130701A1 - Wasch- oder reinigungsmittel mit modifizierten riechstoffen - Google Patents
Wasch- oder reinigungsmittel mit modifizierten riechstoffen Download PDFInfo
- Publication number
- WO2012130701A1 WO2012130701A1 PCT/EP2012/055045 EP2012055045W WO2012130701A1 WO 2012130701 A1 WO2012130701 A1 WO 2012130701A1 EP 2012055045 W EP2012055045 W EP 2012055045W WO 2012130701 A1 WO2012130701 A1 WO 2012130701A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- fragrances
- weight
- oil
- metal oxides
- composition according
- Prior art date
Links
Classifications
-
- 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
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/02—Inorganic compounds ; Elemental compounds
- C11D3/12—Water-insoluble compounds
- C11D3/1213—Oxides or hydroxides, e.g. Al2O3, TiO2, CaO or Ca(OH)2
-
- 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
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/50—Perfumes
-
- 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
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/50—Perfumes
- C11D3/502—Protected perfumes
- C11D3/505—Protected perfumes encapsulated or adsorbed on a carrier, e.g. zeolite or clay
-
- 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
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/50—Perfumes
- C11D3/502—Protected perfumes
- C11D3/507—Compounds releasing perfumes by thermal or chemical activation
Definitions
- WO 2010/076803 A2 describes a topical multicomponent system in which at least one component comprises an active substance which is coated with a metal oxide. Detergents or cleaning agents are not described.
- a solution or dispersion of the starting materials is preferably first prepared, and this mixture is advantageously stirred for a period of at least 1 minute at room temperature (21 ° C).
- thermal energy may also be supplied, e.g. by heating to 60 ° C.
- the particle size of the metal oxides used is basically freely selectable. However, it is preferred that the metal oxides particle sizes ⁇ 1000 ⁇ , advantageously ⁇ 500 ⁇ , in a further advantageous manner ⁇ 100 ⁇ , preferably ⁇ 1 ⁇ , in particular ⁇ 0.1 ⁇ . A possible lower limit of the particle size may e.g. at 1 nm or 10 nm.
- the washing or cleaning agent according to the invention makes it possible to produce a fragrance on the substrates treated therewith.
- the invention goes hand in hand with some further advantages.
- a significant advantage is that the invention allows a fragrant effect by Wederbefeuchten.
- objects treated with the washing or cleaning agent according to the invention e.g. Textiles, after which they surprisingly exude a particularly intense fragrance when they are moistened again.
- This effect is beneficial for many processes of daily life.
- a towel washed with the detergent of the invention unfolds on drying e.g. of crockery or the human body, by the absorbed moisture a fragrance effect.
- appropriate underwear e.g. Undershirt, by the body moisture a renewed fragrance effect are triggered.
- This effect ie a re-flow of fragrance after the Wederbetwoeren, does not occur in the application of ordinary detergents or cleaning agents, i. It is usually not expected that a towel exudes fragrance as soon as it is moistened again.
- Another advantage lies in the improvement of the absorption of fragrances from aqueous, preferably surfactant-containing solutions on the treated objects, in particular textiles. This not only affects the fragrances introduced via the reaction products according to the invention, but also benefits the other fragrances which are not introduced into the system via the reaction products according to the invention. This allows for improved efficiency in fragrance use.
- Another advantage lies in the improved fixation of fragrances on soft and hard surfaces, such as textiles, skin and hair or hard surfaces. With improved fixation here is meant an improved, so strong adhesion of the already scented on the objects fragrances.
- Bad-odor components are volatile compounds with kakosmophoren groups, eg. As amine derivatives and sulfur derivatives.
- the present invention can afford not only a targeted release of fragrances, but also a recording and thus reduction of malodors.
- the amount of metal oxide present preferably introduced via the reaction product according to the invention into the washing or cleaning agent, is 0.00001 to 10% by weight, preferably 0.01 to 1% by weight, based on the total washing or cleaning agent is a preferred embodiment of the invention.
- the washing or cleaning agent according to the invention contains 0.0001 to 95 wt .-%, preferably 0.01 to 40 wt .-% surfactants.
- a particularly preferred washing or cleaning agent according to the invention contains
- Another object of the invention is a process for the preparation of a detergent or cleaning agent, wherein a reaction product of fragrances with metal produces oxides and this reaction product combined with the detergent or cleaning agent matrix.
- a reaction product of fragrances with metal produces oxides and this reaction product combined with the detergent or cleaning agent matrix.
- washing or cleaning agent in the context of the invention also includes the aftertreatment agents. These include, in particular, the fabric softeners, the hygiene rinse and the dryer sheets (so-called dryer sheets), but also the textile fresheners and ironing water.
- the corresponding agents preferably contain the usual ingredients for the product category in question.
- a hygiene rinse usually contains active ingredients that, depending on the individual case, can kill a wide range of organisms from viruses, bacteria, fungi.
- active substances such as, for example, alkylbenzyldimethylammonium chloride, are known per se to the person skilled in the art.
- fabric softeners contain softening active ingredients, generally cationic surfactants, preferably esterquats, ie quaternary ammonium compounds having two hydrophobic radicals, each containing an ester group as a so-called predetermined breaking point for easier biodegradation.
- textile fresheners care products for spraying textiles in the household in order to absorb volatile, unpleasant-smelling molecules and to mask them with pleasant scents are referred to as textile fresheners.
- textile fresheners For absorption, in conventional textile Shear eg cyclodextrins used. Drying cloths are intended for use in the tumble dryer. These are wipes on which certain active substances are applied so that the textiles are less wrinkled and less easily electrostatically charged.
- Detergents or cleaning agents according to the invention preferably comprise, in addition to the reaction product according to the invention, at least one, preferably several, active components, in particular washing, care and / or cleaning active components, advantageously selected from the group comprising anionic surfactants, cationic surfactants, amphoteric surfactants, nonionic surfactants, acidifiers , Alkalizing agents, anti-wrinkling compounds, antibacterials, antioxidants, anti redeposition agents, antistatic agents, builders, bleaches, bleach activators, bleach stabilizers, bleach catalysts, ironing aids, fragrances, anti-shrinkage agents, electrolytes, enzymes, colorants, dyes, dye transfer inhibitors, fluorescers , Fungicides, germicides, odor-complexing substances, hydrotropes, rinse aids, complexing agents, preservatives, corrosion inhibitors, optical brighteners, pearlescers, pH adjusters, phobizers and impregnating agents, polymers, swelling and sliding agents, foam inhibitors,
- the derivatives of the fatty alcohols although also their branched-chain isomers, in particular so-called oxo alcohols, can be used for the preparation of usable alkoxylates.
- Useful are accordingly the alkoxylates, in particular the ethoxylates, primary alcohols with linear, in particular dodecyl, tetradecyl, hexadecyl or octadecyl radicals and mixtures thereof.
- suitable alkoxylation products of alkylamines, vicinal diols and carboxylic acid amides which correspond to the said alcohols with respect to the alkyl part, usable.
- the ethylene oxide and / or propylene oxide insertion products of fatty acid alkyl esters and fatty acid polyhydroxyamides are also suitable.
- alkoxylates are those which are obtained by ethoxylation of branched primary alcohols, in particular by ethoxylation of corresponding branched primary alcohols having 1 to 36 carbon atoms and an average of 0.7 to 3.0 branches per molecule, which branches include methyl and ethyl branches.
- Such alkoxylates are described in US Pat. No. 7,871,973 B1.
- Nonionic surfactant is preferably present in detergents or cleaners according to the invention in amounts of from 0.1% by weight to 30% by weight, in particular from 1% by weight to 25% by weight, based on the weight entire washing or cleaning agent.
- Cationic surfactants can also be present optionally in the detergents or cleaners according to the invention, in particular in the laundry aftertreatment compositions according to the invention.
- cationic surfactants are quaternary ammonium compounds having preferably one or in particular two hydrophobic alkyl radicals.
- Particularly preferred are esterquats, ie quaternary ammonium compounds having two hydrophobic radicals, each containing an ester group as a so-called predetermined breaking point for easier biodegradation.
- the water-soluble organic builder substances include polycarboxylic acids, in particular citric acid and sugar acids, monomeric and polymeric aminopolycarboxylic acids, in particular methylglycinediacetic acid, nitrilotriacetic acid and ethylenediaminetetraacetic acid and polyaspartic acid, polyphosphonic acids, in particular aminotris (methylenephosphonic acid), ethylenediaminetetrakis (methylenephosphonic acid) and 1-hydroxyethane-1, 1 -diphosphonic acid, polymeric hydroxy compounds such as dextrin and also polymeric (poly) -carboxylic acids, polymeric acrylic acids, methacrylic acids, maleic acids and mixed polymers thereof, which may also contain polymerized small amounts of polymerizable substances without carboxylic acid functionality.
- polycarboxylic acids in particular citric acid and sugar acids
- monomeric and polymeric aminopolycarboxylic acids in particular methylglycinediacetic acid, nitrilotriace
- Suitable, albeit less preferred, compounds of this class are copolymers of acrylic acid or methacrylic acid with vinyl ethers, such as vinylmethyl ethers, vinyl esters, ethylene, propylene and styrene, in which the proportion of the acid is at least 50% by weight.
- the optionally usable foam inhibitors include, for example, organopolysiloxanes and mixtures thereof with microfine, optionally silanized silica and paraffin waxes and mixtures thereof with silanated silica or bis-fatty acid alkylenediamides.
- mixtures of different foam inhibitors can be used, for example those of silicones, paraffins or waxes.
- the optional foam inhibitors, in particular silicone and / or paraffin-containing foam inhibitors are bound to a granular, water-soluble or dispersible carrier substance.
- mixtures of paraffin waxes and bistearylethylenediamides are preferred.
- the optionally applicable graying inhibitors have the ability to keep suspended from the textile fiber dirt suspended in the fleet.
- Water-soluble colloids of mostly organic nature are suitable for this purpose, for example starch, glue, gelatin, salts of ether carboxylic acids or ether sulfonic acids of starch or of cellulose or salts of acidic sulfuric acid esters of cellulose or starch.
- water-soluble polyamides containing acidic groups are suitable for this purpose.
- starch derivatives can be used, for example aldehyde starches.
- alcohols and / or organic solvents can be used with up to 50%.
- a liquid, hydrophobic compound selected from limonene, dioctyl ether, lauric acid hexyl ester, decamethylcyclopentasiloxane, C.sub.1-isoparaffin and mixtures thereof, preferably in combination with fatty acid soap and / or unneutralized fatty acid.
- anionic surfactants such as preferably alkylbenzenesulfonate, alkylsulfate, e.g. in amounts of preferably 5-30% by weight
Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP12710720.9A EP2691504B1 (de) | 2011-03-29 | 2012-03-22 | Wasch- oder reinigungsmittel mit modifizierten riechstoffen |
ES12710720.9T ES2609630T3 (es) | 2011-03-29 | 2012-03-22 | Agentes de lavado o de limpieza con fragancias modificadas |
US14/038,952 US8815786B2 (en) | 2011-03-29 | 2013-09-27 | Detergents or cleaning agents containing reaction products of odorants with metal oxides |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE102011006315.3 | 2011-03-29 | ||
DE102011006315A DE102011006315A1 (de) | 2011-03-29 | 2011-03-29 | Wasch- oder Reinigungsmittel mit modifizierten Riechstoffen |
Related Child Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US14/038,952 Continuation US8815786B2 (en) | 2011-03-29 | 2013-09-27 | Detergents or cleaning agents containing reaction products of odorants with metal oxides |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2012130701A1 true WO2012130701A1 (de) | 2012-10-04 |
Family
ID=45888213
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/EP2012/055045 WO2012130701A1 (de) | 2011-03-29 | 2012-03-22 | Wasch- oder reinigungsmittel mit modifizierten riechstoffen |
Country Status (5)
Country | Link |
---|---|
US (1) | US8815786B2 (deFl) |
EP (1) | EP2691504B1 (deFl) |
DE (1) | DE102011006315A1 (deFl) |
ES (1) | ES2609630T3 (deFl) |
WO (1) | WO2012130701A1 (deFl) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2014162311A1 (en) * | 2013-04-01 | 2014-10-09 | Yissum Research Development Company Of The Hebrew University Of Jerusalem Ltd. | Adjustable sol-gel-based capsules comprising fragrances and aromas, and uses thereof |
US9953588B1 (en) * | 2014-03-25 | 2018-04-24 | E Ink Corporation | Nano-particle based variable transmission devices |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN109414020A (zh) | 2016-05-12 | 2019-03-01 | 应用银股份有限公司 | 将金属离子分配到洗涤系统中的制品和方法 |
CN110113946A (zh) | 2016-10-31 | 2019-08-09 | 应用银股份有限公司 | 向分批式洗衣机和烘干机中分配金属离子 |
Citations (17)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB1270040A (en) * | 1967-01-27 | 1972-04-12 | Unilever Ltd | Liquid detergent compositions |
GB1505493A (en) * | 1974-03-07 | 1978-03-30 | Unilever Ltd | Preparation of detergent bars |
EP0536942A2 (en) * | 1991-10-02 | 1993-04-14 | Unilever Plc | Perfume particles |
WO1997047720A2 (en) * | 1996-06-11 | 1997-12-18 | The Procter & Gamble Company | Process for producing a particulate laundry additive for perfume delivery having improved physical properties |
DE19841147A1 (de) | 1998-09-09 | 2000-03-16 | Henkel Kgaa | Kiselsäureester |
DE10212121A1 (de) | 2002-03-15 | 2003-09-25 | Bayer Ag | Verfahren zur Herstellung von nano-Zinkoxid-Dispersionen stabilisiert durch hydroxylgruppenhaltige anorganische Polymere |
JP2004180979A (ja) | 2002-12-04 | 2004-07-02 | Ogawa & Co Ltd | 抗菌消臭剤組成物 |
DE10337198A1 (de) | 2003-08-13 | 2005-03-17 | Degussa Ag | Träger auf Basis von Granulaten, die aus pyrogen hergestelltem Siliciumdioxiden hergestellt sind |
DE102006003092A1 (de) | 2006-01-20 | 2007-07-26 | Henkel Kgaa | 1-Aza-3,7-dioxabicyclo[3.3.0]octan-Verbindungen und ihre Verwendung als Pro-Fragrances |
WO2008077239A1 (en) | 2006-12-22 | 2008-07-03 | Sidense Corp. | A program lock circuit for a mask programmable anti-fuse memory array |
WO2008112826A1 (en) | 2007-03-12 | 2008-09-18 | Board Of Regents, The University Of Texas System | Method and process for the production of multi-coated recognitive and releasing systems |
US20090035365A1 (en) * | 2007-07-30 | 2009-02-05 | Lewis Michael Popplewell | Density Controlled Capsule Particles and Methods of Making the Same |
WO2009103651A2 (en) | 2008-02-21 | 2009-08-27 | Basf Se | Preparation of cationic nanoparticles and personal care compositions comprising said nanoparticles |
DE102008031212A1 (de) | 2008-07-03 | 2010-01-07 | Henkel Ag & Co. Kgaa | Wasch- und Reinigungsmitteladditiv in Partikelform |
DE102008052678A1 (de) | 2008-10-22 | 2010-04-29 | Henkel Ag & Co. Kgaa | Polyoxyalkylenmonoamin modifizierte mehrschichtige Nanopartikel |
WO2010076803A2 (en) | 2009-01-05 | 2010-07-08 | Sol-Gel Technologies Ltd. | Topical systems and kits |
US7871973B1 (en) | 1996-11-26 | 2011-01-18 | Shell Oil Company | Highly branched primary alcohol compositions, and biodegradable detergents made therefrom |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6558710B1 (en) * | 1999-06-14 | 2003-05-06 | Helen Rebecca Godfrey | Topical zinc compositions and methods of use |
US20050191257A1 (en) * | 2004-02-27 | 2005-09-01 | John Brahms | Dry deodorant containing a sesquiterpene alcohol and zinc oxide |
US7833960B2 (en) * | 2006-12-15 | 2010-11-16 | International Flavors & Fragrances Inc. | Encapsulated active material containing nanoscaled material |
WO2008108756A1 (en) * | 2007-03-05 | 2008-09-12 | Grune Guerry L | Sunscreen compositions |
-
2011
- 2011-03-29 DE DE102011006315A patent/DE102011006315A1/de not_active Withdrawn
-
2012
- 2012-03-22 ES ES12710720.9T patent/ES2609630T3/es active Active
- 2012-03-22 WO PCT/EP2012/055045 patent/WO2012130701A1/de active Application Filing
- 2012-03-22 EP EP12710720.9A patent/EP2691504B1/de not_active Not-in-force
-
2013
- 2013-09-27 US US14/038,952 patent/US8815786B2/en not_active Expired - Fee Related
Patent Citations (17)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB1270040A (en) * | 1967-01-27 | 1972-04-12 | Unilever Ltd | Liquid detergent compositions |
GB1505493A (en) * | 1974-03-07 | 1978-03-30 | Unilever Ltd | Preparation of detergent bars |
EP0536942A2 (en) * | 1991-10-02 | 1993-04-14 | Unilever Plc | Perfume particles |
WO1997047720A2 (en) * | 1996-06-11 | 1997-12-18 | The Procter & Gamble Company | Process for producing a particulate laundry additive for perfume delivery having improved physical properties |
US7871973B1 (en) | 1996-11-26 | 2011-01-18 | Shell Oil Company | Highly branched primary alcohol compositions, and biodegradable detergents made therefrom |
DE19841147A1 (de) | 1998-09-09 | 2000-03-16 | Henkel Kgaa | Kiselsäureester |
DE10212121A1 (de) | 2002-03-15 | 2003-09-25 | Bayer Ag | Verfahren zur Herstellung von nano-Zinkoxid-Dispersionen stabilisiert durch hydroxylgruppenhaltige anorganische Polymere |
JP2004180979A (ja) | 2002-12-04 | 2004-07-02 | Ogawa & Co Ltd | 抗菌消臭剤組成物 |
DE10337198A1 (de) | 2003-08-13 | 2005-03-17 | Degussa Ag | Träger auf Basis von Granulaten, die aus pyrogen hergestelltem Siliciumdioxiden hergestellt sind |
DE102006003092A1 (de) | 2006-01-20 | 2007-07-26 | Henkel Kgaa | 1-Aza-3,7-dioxabicyclo[3.3.0]octan-Verbindungen und ihre Verwendung als Pro-Fragrances |
WO2008077239A1 (en) | 2006-12-22 | 2008-07-03 | Sidense Corp. | A program lock circuit for a mask programmable anti-fuse memory array |
WO2008112826A1 (en) | 2007-03-12 | 2008-09-18 | Board Of Regents, The University Of Texas System | Method and process for the production of multi-coated recognitive and releasing systems |
US20090035365A1 (en) * | 2007-07-30 | 2009-02-05 | Lewis Michael Popplewell | Density Controlled Capsule Particles and Methods of Making the Same |
WO2009103651A2 (en) | 2008-02-21 | 2009-08-27 | Basf Se | Preparation of cationic nanoparticles and personal care compositions comprising said nanoparticles |
DE102008031212A1 (de) | 2008-07-03 | 2010-01-07 | Henkel Ag & Co. Kgaa | Wasch- und Reinigungsmitteladditiv in Partikelform |
DE102008052678A1 (de) | 2008-10-22 | 2010-04-29 | Henkel Ag & Co. Kgaa | Polyoxyalkylenmonoamin modifizierte mehrschichtige Nanopartikel |
WO2010076803A2 (en) | 2009-01-05 | 2010-07-08 | Sol-Gel Technologies Ltd. | Topical systems and kits |
Non-Patent Citations (2)
Title |
---|
REDDY, V. R., SYNLETT, vol. 11, 2006, pages 1791 |
SCHMIDT, CHEM. UNSERER ZEIT, vol. 35, no. 3, 2001, pages 176 |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2014162311A1 (en) * | 2013-04-01 | 2014-10-09 | Yissum Research Development Company Of The Hebrew University Of Jerusalem Ltd. | Adjustable sol-gel-based capsules comprising fragrances and aromas, and uses thereof |
US9953588B1 (en) * | 2014-03-25 | 2018-04-24 | E Ink Corporation | Nano-particle based variable transmission devices |
Also Published As
Publication number | Publication date |
---|---|
US8815786B2 (en) | 2014-08-26 |
DE102011006315A1 (de) | 2012-10-04 |
EP2691504B1 (de) | 2016-11-16 |
EP2691504A1 (de) | 2014-02-05 |
US20140024570A1 (en) | 2014-01-23 |
ES2609630T3 (es) | 2017-04-21 |
DE102011006315A8 (de) | 2012-12-20 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
EP3110393B1 (de) | Photolabile duftspeicherstoffe | |
EP2691501B1 (de) | Riechstoffzusammensetzung mit allylethern als riechstoffvorläufer | |
WO2010105873A2 (de) | Lilial-substitut | |
EP2750720B1 (de) | Verfahren zur fehlgeruchsbekämpfung unter verwendung von oxazolidinen | |
EP2408885A1 (de) | Lilial-surrogat | |
WO2008128818A1 (de) | Flüssiges wasch- oder reinigungsmittel mit fliessgrenze | |
EP2655582B1 (de) | Parfümzusammensetzung umfassend riechstoff-aldehyd oder -keton sowie oxazolidin-riechstoffvorläufer | |
EP2440642B1 (de) | Verfahren zur verminderung von schlechtgerüchen | |
EP2691504B1 (de) | Wasch- oder reinigungsmittel mit modifizierten riechstoffen | |
WO2008128817A1 (de) | Flüssiges textilbehandlungsmittel | |
EP2809760B1 (de) | Verfahren zur verminderung von schlechtgerüchen | |
EP2440643A1 (de) | Duftgebendes wasch-, reinigungs- oder pflegemittel | |
WO2008116768A1 (de) | Antimilbenmittel | |
WO2017045891A1 (de) | Diazirine als photocages, die doppelbindungen enthaltende moleküle freisetzen | |
DE102011005947A1 (de) | Diels-Alder-Addukte als thermisch spaltbare Riechstoffvorläufer | |
WO2008145424A1 (de) | Wasch- oder reinigungsmittel mit flüssiger, gelförmiger oder pastenartiger konsistenz | |
EP3368503B1 (de) | Photolabile duftspeicherstoffe | |
WO2010142480A1 (de) | Duftgebendes wasch-, reinigungs- oder pflegemittel | |
WO2017045892A1 (de) | Freisetzung von riechstoffen aus mikrokapseln |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
121 | Ep: the epo has been informed by wipo that ep was designated in this application |
Ref document number: 12710720 Country of ref document: EP Kind code of ref document: A1 |
|
REEP | Request for entry into the european phase |
Ref document number: 2012710720 Country of ref document: EP |
|
WWE | Wipo information: entry into national phase |
Ref document number: 2012710720 Country of ref document: EP |
|
NENP | Non-entry into the national phase |
Ref country code: DE |