EP0847439A1 - Enzymhaltige waschmittelformulierung - Google Patents

Enzymhaltige waschmittelformulierung

Info

Publication number
EP0847439A1
EP0847439A1 EP97930465A EP97930465A EP0847439A1 EP 0847439 A1 EP0847439 A1 EP 0847439A1 EP 97930465 A EP97930465 A EP 97930465A EP 97930465 A EP97930465 A EP 97930465A EP 0847439 A1 EP0847439 A1 EP 0847439A1
Authority
EP
European Patent Office
Prior art keywords
weight
formulation according
butyl
detergent
alkyl
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
Application number
EP97930465A
Other languages
German (de)
English (en)
French (fr)
Inventor
Werner Antwerpen
Fritz Engelhardt
Manfred Müller
Alexander Lerch
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Clariant Produkte Deutschland GmbH
Original Assignee
Clariant GmbH
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Clariant GmbH filed Critical Clariant GmbH
Publication of EP0847439A1 publication Critical patent/EP0847439A1/de
Withdrawn legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16Organic compounds
    • C11D3/38Products with no well-defined composition, e.g. natural products
    • C11D3/386Preparations containing enzymes, e.g. protease or amylase
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/02Anionic compounds
    • C11D1/12Sulfonic acids or sulfuric acid esters; Salts thereof
    • C11D1/28Sulfonation products derived from fatty acids or their derivatives, e.g. esters, amides

Definitions

  • the present invention relates to an enzyme-containing detergent formulation which is characterized by a content of a compound of the general formula I.
  • Enzyme-containing detergent formulations are formulations that are used in addition to usual ones
  • Basic materials such as anionic, nonionic and cationic surfactants, builders, bleaching systems etc.
  • Enzymes such as proteases, amylases,
  • Contain lipases etc.
  • the function of these enzymes is to remove protein, starch or fatty stains from the fabric to be washed.
  • Enzyme-containing detergents of this type are already known and, for example, in
  • EP-A 496315 describes stable and homogeneous aqueous formulations of surfactants with an HLB value of less than or equal to 13, which additionally contain compounds obtainable by reacting unsaturated fatty acids with amines and subsequent sulfonation.
  • the object of the present invention is to provide a detergent formulation which can also remove blood stains in a satisfactory manner. This object is surprisingly achieved by adding a compound of the general formula I to an enzyme-containing detergent formulation.
  • the present invention accordingly relates to an enzyme-containing detergent formulation, characterized in that it is a compound of the general Formula I.
  • B represents NR 1 R 2 , (C r C 8 ) alkoxy, OH or OM 1 ;
  • R 1 is (C 1 -C 8 ) alkyl, (C 2 -C 8 ) alkenyl, phenyl, alkylphenyl or phenalkyl, each with
  • R 2 represents hydrogen or has one of the meanings of R 1 or in which R and R 2 together with the N atom carrying them form a heterocyclic radical;
  • M and M 1 independently of one another for an alkali metal, triethanolammonium or ammonium cation or an equivalent of an alkaline earth metal or
  • n and n each independently represent a number from 0 to 22; contains.
  • A preferably represents a group of the formula
  • B preferably represents NR 1 R 2 R 1 or R 2 (C r C 8 ) -alkyl can be straight-chain or branched and is, for example, methyl, ethyl, n-propyl, i-propyl, n-butyl, i-butyl, sec-butyl, tert .-Butyl, n-pentyl, n-hexyl, n-heptyl or n-octyl. The same applies to (C 2 -C 8 ) alkenyl.
  • Alkylphenyl with 1 to 4 carbon atoms in the alkyl chain is, for example, methyl, ethyl, propyl or butylphenyl.
  • Phenalkyl with 1 to 4 carbon atoms in the side chain is, for example, benzyl or phenethyl.
  • a heterocyclic radical formed by R 1 , R 2 and the N atom carrying them is in particular 5- or 6-membered and can be saturated, unsaturated or partially unsaturated. In addition, it can also contain further hetero elements from the series N, 0 and S. Examples of such heterocyclic radicals are the piperidine, morpholine, thiophene, tetrahydrofuran or tetrahydrothiophene radical.
  • R 1 and R 2 denote methyl, ethyl, propyl, i-propyl, n-butyl, i-butyl, sec-butyl, tert-butyl, n-pentyl, n-hexyl, n- Heptyl, n-octyl, i-octyl, vinyl, allyl, methallyl or crotyl or R 1 and R 2 together with the N atom carrying them form a piperidine or morpholine ring.
  • R 1 and R 2 are n-butyl, R 1 is methyl and R 2 is phenyl or R 1 and R 2 together with the N atom carrying them form a morpholine ring.
  • An alkali indication for M or M 1 can be, for example, the cation of lithium, sodium or potassium.
  • An equivalent of M or M 1 of an alkaline earth metal cation can be derived, for example, from magnesium, calcium or barium.
  • M and M 1 preferably independently of one another represent the ammonium, sodium or potassium cation.
  • the sodium cation is particularly preferred.
  • m and n preferably each independently represent a number from 2 to 12, particularly preferably a number from 6 to 8.
  • the detergent formulations according to the invention preferably contain the compounds of the general formula 1 in amounts of 0.1 to 6% by weight, particularly preferably in amounts of 1 to 5% by weight, based on the total amount of detergent.
  • the enzymes contained in the detergent formulations according to the invention are, for example, commercially available proteases, amylases, lipases, cellulases or peroxidases. Mixtures of the enzymes mentioned can also be used.
  • These enzymes are preferably present in amounts of 0.5 to 2.0% by weight, particularly preferably in amounts of 0.8 to 1.2% by weight, based on the total amount of detergent.
  • the detergent formulations according to the invention are based on commercially available ingredients known to those skilled in the art.
  • suitable ingredients are, for example, anionic surfactants, such as, for example, alkyl sulfates, alkyl ether sulfates, linear alkylbenzenesulfonate, secondary alkanesulfonate, C 8 -C 24 -olefin sulfonates, phosphates, as are usually used in detergents, and other anionic surfactants, as described, for example, in WO92 / 06160 are nonionic surfactants, such as, for example, fatty alcohol polyglycol ethers, fatty acid amide polyglycol ethers, alkylphenol polyglycol ethers and cationic, zwitterionic or amphoteric surfactants, such as, for example, alkylbetaines, alkylaminobetaines, sulfobetaines and aminoglycinates.
  • anionic surfactants
  • the ingredients in powder detergent formulations are preferably present in amounts of 92 to 99.4% by weight, particularly preferably in amounts of 93 to 97% by weight, based on the total amount of detergent.
  • the ingredients are preferably present in amounts of 35 to 60% by weight, particularly preferably in amounts of 40 to 50% by weight, based on the total amount of detergent.
  • the detergent formulations according to the invention can also contain other customary auxiliaries and additives. Examples are fragrances, dyes, disinfectants, corrosion inhibitors, bleach / activators, dye transfer inhibitors, etc.
  • the compounds of general formula I can be prepared, for example, by reacting unsaturated fatty acids of general formula II
  • R 1 and R 2 are as defined above and sulfuric acid.
  • Suitable examples of fatty acids of the general formula II are in particular oleic acid, ricin fatty acids and elaidic acid.
  • the synthesis of the compounds of the general formula I mentioned generally gives rise to mixtures of compounds of the general formula I, which may also contain unreacted fatty acids of the general formula II.
  • the individual compounds of the general formula I can be obtained in pure form from these mixtures by methods known to the person skilled in the art. As a rule, however, this is not necessary since the mixtures mentioned can be used directly in the detergent formulations according to the invention.
  • the detergent formulations according to the invention can be prepared, for example, by simply mixing the individual components, which can be followed by spray drying, agglomeration or extrusion. Those skilled in the art are familiar with these procedures.
  • the detergent formulations according to the invention achieve the stated object in an outstanding manner. Surprisingly, it was found that the compounds of the general formula I also have a softening effect and sustainably improve the feel of test fabrics, for example a terry towel.
  • a powder detergent formulation is obtained from elaidic acid with dimethylamine and sulfuric acid, which can remove blood stains in a satisfactory manner.
  • Example 1 If a reaction product of ricinoleic acid with dipropylamine and sulfuric acid is used in Example 1 instead of the reaction product of elaidic acid with dimethylamine and sulfuric acid, an equally good detergent formulation is obtained.
  • Spray-dried detergent made from 7.5% by weight Na-C 12 alkylbenzenesulfonate, 3.0% by weight Na-C 16/18 alkyl sulfate, 6.0% by weight of an ethoxylated fatty alcohol, 7.0% by weight soda, 11 , 0% by weight layered silicate SKS 6, 17.0% by weight zeolite A, 5.0% by weight Na citrate, 5.0% by weight Borax, 20.0% by weight percarbonate, 5.0% by weight TAED, 0.5
  • phosphonates 6.0% by weight polymers, 1.0% by weight enzymes (protease, lipase, cellulase), 0.2% by weight of a commercially available optical brightener and 5.8% by weight of a reaction product from oleic acid, Methylphenylamine and sulfuric acid.
  • the product can remove blood stains satisfactorily.
  • a liquid detergent By mixing 11.0% by weight of a secondary Na alkanesulfonate, 16.0% by weight of soap, 12.0% by weight of an ethoxylated fatty acid alcohol, 5.0% by weight of Na citrate, 1.0% by weight Phosphonates, 0.5% by weight of polymers, 1.1% by weight of enzymes (protease, lipase, cellulase), 0.2% by weight of a commercially available optical brightener, 3.0% by weight of ethanol, 5.0% by weight 1, 2-propylene glycol and 2.0% by weight of a reaction product of elaidic acid with dipropylamine and sulfuric acid and subsequent filling with water to 100% by weight, a liquid detergent is obtained which can remove blood stains in a satisfactory manner.
  • the lightening of the test stains was determined after washing by reflectance measurements using Elrepho 2000.
  • Example 6 The procedure was analogous to Example 6, with a terry towel as the test fabric and about 2.3 kg of cotton fabric as ballast. The following was compared: a) 100 g of liquid detergent b) 95 g of liquid detergent + 5 g of a reaction product of oleic acid, di-n-butylamine and sulfuric acid as a 40% aqueous solution.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Wood Science & Technology (AREA)
  • Organic Chemistry (AREA)
  • Detergent Compositions (AREA)
EP97930465A 1996-07-03 1997-07-01 Enzymhaltige waschmittelformulierung Withdrawn EP0847439A1 (de)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
DE1996126620 DE19626620A1 (de) 1996-07-03 1996-07-03 Enzymhaltige Waschmittelformulierung
DE19626620 1996-07-03
PCT/EP1997/003429 WO1998001526A1 (de) 1996-07-03 1997-07-01 Enzymhaltige waschmittelformulierung

Publications (1)

Publication Number Publication Date
EP0847439A1 true EP0847439A1 (de) 1998-06-17

Family

ID=7798712

Family Applications (1)

Application Number Title Priority Date Filing Date
EP97930465A Withdrawn EP0847439A1 (de) 1996-07-03 1997-07-01 Enzymhaltige waschmittelformulierung

Country Status (6)

Country Link
EP (1) EP0847439A1 (pt)
JP (1) JPH11512145A (pt)
BR (1) BR9706536A (pt)
CA (1) CA2230651A1 (pt)
DE (1) DE19626620A1 (pt)
WO (1) WO1998001526A1 (pt)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2732016A1 (de) * 2011-07-12 2014-05-21 Clariant International Ltd. Verwendung von sekundären paraffinsulfonaten zur erhöhung des reinigungsvermögens von enzymen

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2279314A (en) * 1939-01-26 1942-04-14 Lever Brothers Ltd Detergent composition
DE2659696C3 (de) * 1976-12-31 1980-08-21 Hoechst Ag, 6000 Frankfurt Mittel zum Avivieren von Textilmaterial
DE3063434D1 (en) * 1979-05-16 1983-07-07 Procter & Gamble Europ Highly concentrated fatty acid containing liquid detergent compositions
EP0095205B1 (en) * 1982-05-24 1986-10-15 THE PROCTER & GAMBLE COMPANY Fatty acid containing detergent compositions
DE4034840A1 (de) * 1990-11-02 1992-05-07 Henkel Kgaa Enzymatisches fluessigwaschmittel
TW204366B (pt) * 1991-01-19 1993-04-21 Hoechst Ag
RU2000320C1 (ru) * 1991-05-20 1993-09-07 Научно-исследовательский и проектный институт химической промышленности Моющее средство дл стирки
US5474701A (en) * 1994-01-21 1995-12-12 Buckman Laboratories International, Inc. Enzymes for recreational water

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
See references of WO9801526A1 *

Also Published As

Publication number Publication date
MX9801689A (es) 1998-08-30
JPH11512145A (ja) 1999-10-19
CA2230651A1 (en) 1998-01-15
BR9706536A (pt) 1999-07-20
WO1998001526A1 (de) 1998-01-15
DE19626620A1 (de) 1998-01-08

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