DE2758022A1 - Stable liquid catalase compsns. - contg. microbicide as preservative - Google Patents

Stable liquid catalase compsns. - contg. microbicide as preservative

Info

Publication number
DE2758022A1
DE2758022A1 DE19772758022 DE2758022A DE2758022A1 DE 2758022 A1 DE2758022 A1 DE 2758022A1 DE 19772758022 DE19772758022 DE 19772758022 DE 2758022 A DE2758022 A DE 2758022A DE 2758022 A1 DE2758022 A1 DE 2758022A1
Authority
DE
Germany
Prior art keywords
catalase
microbicide
compsns
contg
weight
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Withdrawn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
DE19772758022
Other languages
German (de)
Inventor
Hans F Dipl Chem Dr Pfeiffer
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.)
Henkel AG and Co KGaA
Original Assignee
Henkel AG and Co KGaA
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 Henkel AG and Co KGaA filed Critical Henkel AG and Co KGaA
Priority to DE19772758022 priority Critical patent/DE2758022A1/en
Publication of DE2758022A1 publication Critical patent/DE2758022A1/en
Withdrawn legal-status Critical Current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
    • C11D3/48Medical, disinfecting agents, disinfecting, antibacterial, germicidal or antimicrobial compositions
    • 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
    • C11D3/38663Stabilised liquid enzyme compositions

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)
  • Enzymes And Modification Thereof (AREA)

Abstract

Catalase compsn. according to the Parent Patent comprise aq. solns. or suspensions contg. (a) 0.5-10 wt. % anionic surfactant, (b) 2-50% nonionic surfactant and (c) 500-500,000 Iu/ml of catalase, with an (a) : (b) wt. ratio of 1:1-100. The improvement lies in the fact that the compsns. also contain 0.0005-1 (pref. 0.05-0.5) wt. % of a microbicide. The microbicide acts as a preventive (esp. when the compsns. contain no lower alcohol) without impairing the activity of the catalase.

Description

"Stabiles, flüssiges KataLasepräparat""Stable, liquid KataLase preparation"

Gegenstand des Hauptpatentes (Patentanmeldung P 27 53 679.4, internes Aktenzeichen der Anmelderin D 5676) ist ein stabiles, flüssiges, Katalase enthaltendes Enzympräparat in Form einer wäßrigen Lösung bzw. Suspension, gekennzeichnet durch einen Gehalt an A) 0,5 bis 10 Gewichtsprozent mindestens eines wasserlöslichen Aniontensids aus der Klasse der Sulfonate und/oder Sulfate in Form der Alkalimetall-, Ammonium- oder organischen Ammoniumsalze, B) 2 bis 50 Gewichtsprozent mindestens eines nichtionischen Tensids aus der Klasse der Polyglykolätherderivate, C) Katalase in einer solchen enge, daß die Aktivität des Mittels 500 bis 500 000 internationale Einheiten U/ml beträgt, wobei das Gewichtsverhältnis von anionischem Tensid (A) zu nichtionischem Tensid (B) 1 : 1 bis 1 : 100 beträgt.Subject of the main patent (patent application P 27 53 679.4, internal Applicant's file number D 5676) is a stable, liquid containing catalase Enzyme preparation in the form of an aqueous solution or suspension, characterized by a content of A) 0.5 to 10 percent by weight of at least one water-soluble anionic surfactant from the class of sulfonates and / or sulfates in the form of alkali metal, ammonium or organic ammonium salts, B) 2 to 50 percent by weight of at least one nonionic Surfactants from the class of polyglycol ether derivatives, C) catalase in one of these close that the activity of the agent is 500 to 500,000 international units U / ml is, the weight ratio of anionic surfactant (A) to nonionic Surfactant (B) is 1: 1 to 1: 100.

Gemäß Patentanspruch 6 können bis zu 40 Gewichtsprozent an einwertigen und/oder mehrwertigen Alkoholen bzw. Teiläthern mehrwertiger Alkohole anwesend sein. Diese Zusätze, insbesondere die einwertigen Alkohole üben eine gewisse konservierende Wirkung aus.According to claim 6, up to 40 percent by weight can be monovalent and / or polyhydric alcohols or partial ethers of polyhydric alcohols may be present. These additives, especially the monohydric alcohols, have a certain preservative effect Effect.

Gemäß vorliegender Zusatzanmeldung wird durch Zusatz bestimmter Mikrobizide auch bei Abwesenheit von Alkoholen die Haltbarkeit der Katalasepräparate verbessert. Gegenstand der Erfindung ist demnach ein stabiles, flüssiges Katalasepräparat nach Patent (Patentanmeldung P 27 53 679.4), gekennzeichnet durch einen Gehalt an 0,0005 bis 1 Gew.-%, vorzugsweise 0,05 bis 0,5 Gew.-% eines Mikrobizids Als Katalase kommt außer der im Hauptpatent genannten Bakterienkatalase auch aus Leberpräparaten gewonnene Katalase, insbesondere Rinderleberkatalase, in Frage. Hinsichtlich der Aktivität bzw. der einzusetzenden Mengen gelten die in der Hauptanmeldung gemachten Angaben. Das gleiche gilt für die Art und Menge der anionischen und nichtionischen Tenside sowie der sonstigen dort genannten Zusatzstoffe.According to the present additional application, the addition of certain microbicides The shelf life of catalase preparations is improved even in the absence of alcohol. The invention accordingly provides a stable, liquid catalase preparation according to Patent (patent application P 27 53 679.4), characterized by a content of 0.0005 to 1% by weight, preferably 0.05 to 0.5% by weight of a microbicide as In addition to the bacterial catalase mentioned in the main patent, catalase also comes from liver preparations obtained catalase, in particular beef liver catalase, in question. With regard to the Activity or the quantities to be used are those stated in the main application Declarations. The same applies to the type and amount of anionic and nonionic Surfactants and the other additives mentioned there.

Als Mikrobizide eignen sich folgende Verbindungsklassen bzw.The following classes of compounds or

Verbindungen, die keine Eiweißdenaturierung bewirken bzw.Compounds that do not cause protein denaturation or

frei von acylierenden Gruppen sind.are free from acylating groups.

1. Aromatische Kohlenwasserstoffe, z.B. Toluol.1. Aromatic hydrocarbons such as toluene.

2. Phenole und halogenierte Phenole, z.B. o-Phenylphenol, 2-Benzylphenol, p-Hydroxybenzoesäure, p-Chlor-m-kresol, 4-Chlor-3,5-xylenol, 2,4-Dichlor-3,5-xylenol, p-Chlor-ophenylphenol, 2-Benzyl-4-chlorphenol.2. Phenols and halogenated phenols, e.g. o-phenylphenol, 2-benzylphenol, p-hydroxybenzoic acid, p-chloro-m-cresol, 4-chloro-3,5-xylenol, 2,4-dichloro-3,5-xylenol, p-chloro-ophenylphenol, 2-benzyl-4-chlorophenol.

Hiervon kommen in erster Linie die einkernigen Phenolderivate in Frage, da die antimikrobielle Aktivität der mehrkernigen durch die Niotenside herabgesetzt wird. Of these, the mononuclear phenol derivatives are primarily used Question, since the antimicrobial activity of the polynuclear is reduced by the nonionic surfactants will.

3. Trichlorcarbanilid.3. Trichlorocarbanilide.

4. Bromnitroverbindungen, z.B. 2-Brom-2-nitropropandiol, 5-Brom-5-nitro- 1, 3-dioxan.4. Bromonitro compounds, e.g. 2-bromo-2-nitropropanediol, 5-bromo-5-nitro- 1, 3-dioxane.

5. Organische Quecksilberverbindungen, z.B. Phenylquecksilberacetat, Phenylquecksilberborat, Xthylquecksilber-thiosalicylat-Natrium.5. Organic mercury compounds, e.g. phenyl mercury acetate, Phenyl mercury borate, ethyl mercury thiosalicylate sodium.

Auch Gemische verschiedener Mikrobizide können verwendet werden.Mixtures of different microbicides can also be used.

Die genannten Mikrobizide verleihen den Mitteln gemäß Hauptpatent eine größere Beständigkeit auch in Abwesenheit von niedermolekularen Alkoholen, wie Methanol oder Äthanol, ohne gleichzeitig die Aktivität der Katalase zu beeinträchtigen.The microbicides mentioned give the agents according to the main patent greater resistance even in the absence of low molecular weight alcohols, like methanol or ethanol, without impairing the activity of the catalase at the same time.

Im Falle der Konservierung mit aromatischen Kohlenwasserstoffen, wie Toluol, eignen sich die Mittel insbesondere zum Einsatz in der Gummi- und Kunststoffverarbeitung.In the case of preservation with aromatic hydrocarbons, such as Toluene, the agents are particularly suitable for use in rubber and plastics processing.

Im übrigen sind die Verwendungsrnöglichkeiten der konservierten Mittel die gleichen wie im Hauptpatent angegeben.In addition, the possible uses of the preserved funds the same as stated in the main patent.

Beispiel Es wurde ein Mittel folgender Zusamr.lensetzung hergestellt (in Gew.-%): Katalase (Aktivität 550 U/mg) 5,0 Alkylbenzolsulfonat 2,5 C16-C13-Fettalkohol + 10 Äthylenoxid 10,0 Wasser Rest Das Mittel wurde 48 Std. bei Raumtemperatur in einer geöffneten Flasche aufbewahrt und anschließend 10 Tage verschlossen bei einer Temperatur von 30 OC gelagert. Die Keimzahl betrug danach 4.105 pro ml.Example A product was prepared with the following composition (in% by weight): catalase (activity 550 U / mg) 5.0 alkylbenzenesulfonate 2.5 C16-C13 fatty alcohol + 10 ethylene oxide 10.0 water remainder The agent was 48 hours at room temperature in stored in an opened bottle and then sealed for 10 days in a Stored at a temperature of 30 OC. The number of germs was then 4,105 per ml.

Bei einem Zusatz Toluol in Mengen von 0,05 Gew.-% (Versuch 1) bzw. 0,1 Gew.-% (Versuch 2) wurden unter gleichen Bedingungen lediglich 2.102 Keime (versuch 1) bzw. 40 Keime (Versuch 2) aufgefunden.If toluene is added in amounts of 0.05% by weight (experiment 1) or 0.1% by weight (experiment 2) only 2,102 germs (experiment 1) or 40 germs (experiment 2) found.

Die Alkalase-Aktivität war innerhalb der Versuchsdauer nicht meßbar abgesunken.The alkalase activity was not measurable within the duration of the experiment sunk.

Claims (2)

"Stabiles, flüssiges Katalasepräparat" Zusatzanmeldung zur Patentanmeldung P 27 53 679.4 (D 5676) Patentansprüche 1. Stabiles, flüssiges Katalasepräparat nach Patent (Patentanmeldung P 27 53 679.4>, gekennzeichnet durch einen Gehalt an 0,0005 bis 1 Gew.-%, vorzugsweise 0,05 bis 0,5 Gew.-% eines Mikrobizids. "Stable, liquid catalase preparation" additional application to the patent application P 27 53 679.4 (D 5676) claims 1. Stable, liquid catalase preparation according to Patent (patent application P 27 53 679.4>, characterized by a content of 0.0005 to 1% by weight, preferably 0.05 to 0.5% by weight of a microbicide. 2. Mittel nach Anspruch 1, dadurch gekennzeichnet, daß das Mikrobizid aus mindestens einer Verbindung aus der Klasse der aromatischen Kohlenwasserstoffe, der gegebenenfalls halogenierten Phenole, des Trichlorcarbanilids, der Bromnitroverbindungen und der organischen Quecksilberverbindungen besteht.2. Composition according to claim 1, characterized in that the microbicide from at least one compound from the class of aromatic hydrocarbons, the optionally halogenated phenols, the trichlorocarbanilide, the bromonitro compounds and the organic mercury compounds.
DE19772758022 1977-12-24 1977-12-24 Stable liquid catalase compsns. - contg. microbicide as preservative Withdrawn DE2758022A1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
DE19772758022 DE2758022A1 (en) 1977-12-24 1977-12-24 Stable liquid catalase compsns. - contg. microbicide as preservative

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE19772758022 DE2758022A1 (en) 1977-12-24 1977-12-24 Stable liquid catalase compsns. - contg. microbicide as preservative

Publications (1)

Publication Number Publication Date
DE2758022A1 true DE2758022A1 (en) 1979-06-28

Family

ID=6027295

Family Applications (1)

Application Number Title Priority Date Filing Date
DE19772758022 Withdrawn DE2758022A1 (en) 1977-12-24 1977-12-24 Stable liquid catalase compsns. - contg. microbicide as preservative

Country Status (1)

Country Link
DE (1) DE2758022A1 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0224971A2 (en) * 1985-12-06 1987-06-10 Unilever N.V. Enzymatic liquid detergent composition

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0224971A2 (en) * 1985-12-06 1987-06-10 Unilever N.V. Enzymatic liquid detergent composition
EP0224971A3 (en) * 1985-12-06 1988-09-07 Unilever Nv Enzymatic liquid detergent composition

Similar Documents

Publication Publication Date Title
EP0252278B1 (en) Disinfecting agents and their use in disinfecting the skin and mucous membranes
DE60008868T2 (en) LIQUID CONCENTRATES LIKE COSMETIC CONSERVATIVE
DE69821995T2 (en) ANTIMICROBIAL COMPOSITION
EP0087049B1 (en) Concentrate of disinfecting agent
DE2539016A1 (en) DISINFECTANT
EP0977825A1 (en) Liquid enzyme preparation and the use thereof
WO1993001714A1 (en) Mixtures with an antimicrobial action
Corner et al. Toxicity of oil-spill removers (‘detergents’) to marine life: an assessment using the intertidal barnacle Elminius modestus
EP0683628B1 (en) Anti-parasitic disinfectant
DE680599C (en) Procedure for disinfection and preservation
DE3636541A1 (en) DISINFECTANT WITH PARASITE KILLING EFFECT
EP0243713A2 (en) Bactericidal composition and use thereof
DE2758022A1 (en) Stable liquid catalase compsns. - contg. microbicide as preservative
US5635492A (en) Teat treating compositions, production and use
US5091174A (en) Preservative for biological specimens
EP0940145B1 (en) O/W microemulsions containing one or more salts of alkylthiouronium and/or alpha-omega-alkylendithiouronium as microbiocidal agents and their use for manual or automated disinfection of instruments
US2874087A (en) Disinfectant compositions
EP0385369B1 (en) Method for the antimicrobiol preservation of surfactant
EP0620013B1 (en) Desinfectant for toilet systems with holding tanks and similar equipment
EP0433516A1 (en) Preservative for biological specimens
DE10224978A1 (en) Glycerin ether as a preservative for cooling lubricants
DE60115461T2 (en) CARRIER SOLUTION FOR GLAZABLE CONCENTRATIONS OF FREEZING PREPARATIONS AND FREEZER COMPOUND MIXES
DE2640790A1 (en) COMPOUNDS CONTAINING BETA-SUBSTITUTED ALLYL ALCOHOLS AND THEIR SULFUR ACID ESTERS, PHOSPHORIC ACID ESTERS, ALKANOYLESTER AND ALKYLENE OXYD ETHER
EP0188026B1 (en) Disinfactant compositions
DE19508654B4 (en) Tuberculocidal disinfectant and its use

Legal Events

Date Code Title Description
8141 Disposal/no request for examination