EP2773739A1 - Composition liquide de nettoyage antimicrobien de surfaces dures - Google Patents

Composition liquide de nettoyage antimicrobien de surfaces dures

Info

Publication number
EP2773739A1
EP2773739A1 EP12769078.2A EP12769078A EP2773739A1 EP 2773739 A1 EP2773739 A1 EP 2773739A1 EP 12769078 A EP12769078 A EP 12769078A EP 2773739 A1 EP2773739 A1 EP 2773739A1
Authority
EP
European Patent Office
Prior art keywords
composition
weight
hard surface
terpineol
thymol
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.)
Granted
Application number
EP12769078.2A
Other languages
German (de)
English (en)
Other versions
EP2773739B1 (fr
Inventor
Sameer Keshav Barne
Amit Chakrabortty
Maya Treesa Saji
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.)
Unilever PLC
Unilever NV
Original Assignee
Unilever PLC
Unilever NV
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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=46980938&utm_source=***_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=EP2773739(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Unilever PLC, Unilever NV filed Critical Unilever PLC
Priority to PL12769078T priority Critical patent/PL2773739T3/pl
Publication of EP2773739A1 publication Critical patent/EP2773739A1/fr
Application granted granted Critical
Publication of EP2773739B1 publication Critical patent/EP2773739B1/fr
Active legal-status Critical Current
Anticipated expiration legal-status Critical

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
    • C11D3/20Organic compounds containing oxygen
    • C11D3/2003Alcohols; Phenols
    • C11D3/2006Monohydric alcohols
    • C11D3/2037Terpenes
    • 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
    • C11D3/20Organic compounds containing oxygen
    • C11D3/2075Carboxylic acids-salts thereof
    • C11D3/2082Polycarboxylic acids-salts thereof
    • 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
    • C11D3/26Organic compounds containing nitrogen
    • C11D3/30Amines; Substituted amines ; Quaternized amines

Definitions

  • the invention relates to a liquid hard surface cleaning and disinfection composition.
  • the invention more particularly relates to a hard surface disinfection composition that
  • Liquid compositions for disinfecting and cleaning hard surfaces like floors, walls, windows, doors, furniture, and table tops in various indoor and outdoor locations are known. Toilets and bathrooms are other places where germs proliferate and
  • disinfection and cleaning compositions in liquid form are widely used.
  • Other types of hard surfaces that are cleaned by such compositions include utensils and other articles found in households, offices and other public places.
  • ⁇ microbials Two of the popular classes of disinfecting / sanitizing actives are (i) bleaches and (ii) phenolics.
  • Halogen and active oxygen are two most effective bleaches.
  • Bleaches are compounds that liberate oxidising agents like chlorine, bromine, fluorine, nascent oxygen or other oxidizing agents that break the cell walls of microbes like bacteria and virus thereby disinfecting the surfaces thus treated.
  • Phenolics are another class of anti ⁇ microbials often derived from essential oils extracted from natural sources which are formulated in an emulsified form and sold as floor and toilet cleaners.
  • compositions include surfactants to either
  • This invention has the advantage that essential oil actives like terpineol and thymol have a strong medicinal odour which is not liked by some consumers and it is advantageous to include thymol and
  • terpineol at lower concentrations while ensuring that same efficient anti-microbial action. Further, it has been found by way of the present invention that inclusion of a chelating agent sodium tripolyphosphate provides for further enhanced antibacterial efficacy.
  • Liquid hard surface cleaning compositions having a pH 9 to 12 comprising cationic surfactant are known.
  • Another object of the present invention is to provide a liquid hard surface cleaning and disinfecting composition that has relatively fast antimicrobial action.
  • composition with a pH in the range of 9 to 12 comprising
  • a method of cleaning and disinfecting a hard surface comprising applying to said hard surface a composition of the first aspect diluted with water in a weight ratio of 1: 20 to 1: 200.
  • the first aspect of the invention provides for a liquid hard surface antimicrobial cleaning composition with a pH in the range of 9 to 12.
  • the composition comprises 0.5 to 4% by weight of benzalkonium chloride; 0.25 to 3% by weight of salt of di or tri carboxylic acid; 0.01 to 2% by weight of an essential oil active selected from thymol or terpineol; and 87 to 97% by weight water.
  • the composition comprises 0.5 to 4%, more preferably 1 to 2%, further more preferably 1.25 to 1.75% cationic surfactant benzalkonium chloride.
  • the composition comprises 0.25 to 3%, preferably 0.5 to 2%, more preferably 0.5 to 1.5% by weight of the composition salt of di or tri carboxylic acid.
  • the salt of di or tri carboxylic acid is preferably chosen from an oxalate, fumarate, phthalate, maleate, malate, malonate or citrate.
  • the salt of di or tricarboxylic acid is most preferably a phthalate, malate, malonte, or citrate.
  • Alkali metal or alkaline earth metal salts are preferred, more preferably alkali metal salts of which sodium salt is most preferred. Structure of salts of some of the carboxylic acids are given below:
  • the composition comprises an essential oil antimicrobial active selected from thymol or terpineol at 0.01 to 2% by weight of the composition.
  • Preferred antimicrobial compositions of the present invention have thymol higher than 0.05 and lesser than 0.3% by weight. Thymol may be added to the antimicrobial composition in
  • thyme oil or thyme extract comprising thymol may be added to the antimicrobial
  • Thyme oil or thyme extract is obtained from the thyme plant.
  • Thyme plant refers to a plant belonging be genus Thymus and includes but is not limited to the following
  • Thymus vulgaris Thymus zygis , Thymus satureoides, Thymus mastichina , Thymus broussonetti , Thymus maroccanus , Thymus pallidus , Thymus algeriensis , Thymus serpyllum, Thymus pulegoide, and Thymus citriodorus .
  • Preferred antimicrobial compositions of the present invention have terpineol higher than 0.05 and lesser than 1% by weight.
  • the terpineol is preferably selected from alpha-terpineol , beta-terpineol , gamma-terpineol or mixtures thereof. It is particularly preferred that the terpineol is alpha-terpineol.
  • Terpineol may be added to the antimicrobial composition in purified form. Alternatively pine oil comprising terpineol may be added to the antimicrobial composition.
  • the composition optionally comprises sodium tripoly phosphate (STPP) .
  • STPP sodium tripoly phosphate
  • composition of the invention comprises water as a preferred carrier. Water is present in 87 to 97%, preferably 90 to 95% by weight of the composition.
  • composition of the invention optionally comprises a
  • surfactant is a non-ionic surfactant.
  • Non-ionic surfactant is preferably present in an amount of 2 to 10% by weight of the composition.
  • Particularly preferred nonionic surfactants are fatty alcohol ethoxylates preferably C8-C22, more preferably C8-C16 fatty alcohol ethoxylates, comprising between 1 and 8 ethylene oxide groups.
  • Suitable surfactant concentrations in liquid form of hard surface cleaning compositions are preferably from 1 to 5 % by weight of the composition.
  • the composition of the invention has pH in the range of 9 to 12, preferably in the range of 10.5 to 11.5. This could be achieved by incorporating the essential ingredients of the invention in selected amounts, else may be achieved by
  • the alkaline agent is a compound having a hydrophilic property and a hydrophilic property.
  • the alkaline agent is preferably present in 0.1 to 1% by weight of the composition .
  • composition of the invention can be achieved in the absence of conventional disinfectants like bleaches e.g. halogens, halogenated
  • bleaches compounds and active oxygen based bleaches.
  • small amount of such bleaches may be present in the composition e.g. less than 1%, preferably less than 0.5%, more preferably less than 0.1% and the efficacy of the composition is achievable even with the bleaches being absent from the composition.
  • composition may further comprise various additional ingredients known to a person skilled in the art.
  • additional ingredients known to a person skilled in the art.
  • additional ingredients include but are not limited to:
  • perfumes perfumes, pigments, preservatives, emollients, sunscreens, emulsifiers, gelling agents, or thickening agents.
  • the antimicrobial composition may be in form of a liquid but the liquid composition may be further thickened to a gel or a paste.
  • the antimicrobial composition of the present invention can be used for cleansing and care of hard surfaces such as glass, metal, plastic, wood, ceramic and the like.
  • a method of cleaning and disinfecting a hard surface comprising applying to said hard surface a composition of the invention diluted with water in a weight ratio of 1: 20 to 1: 200, preferably in a ratio of 1:40 to 1:80.
  • the method preferably comprises a step of rinsing the surface with a suitable solvent preferably water or the surface may be wiped with a suitable wipe.
  • composition of the invention provides an antimicrobial action where the contact time of the antimicrobial actives with the surface is low, i.e. of the order of less than 5 minutes, preferably less than 2 minutes, further more preferably less than a minute and in many cases less than 15 seconds.
  • Antibacterial compositions for hard surface cleaning as shown in Table - 1 read along with Table - 2 were prepared.
  • the compositions were tested for antibacterial efficacy using the European Suspension Test BS EN1276 which is briefly described below:
  • test suspension of bacteria (1 ml) was added to a sample of the product under a certain dilution condition (8 ml) along with a specific soil (1 ml) .
  • the mixture was maintained at 20°C for 5 minutes. After this period of contact time, an aliquot was taken and was immediately neutralized by a validated method.
  • the number of bacteria in each sample were determined by plating in TSA agar and the reduction in viable count was calculated after incubating for 48 hours.
  • aeruginosa ATCC 15442 (at 10 7 cfu/ml concentration) ; the dilution was 1:60 of the product (a floor cleaner) in hard water.
  • the soil used was used was Bovine Serum Albumin (BSA) at a final concentration of 0.03%.
  • BSA Bovine Serum Albumin
  • the pH of the samples was 11.0. Table - 1
  • Table - 2 Compositions as per Table - 1 where prepared using the di/carboxylic acids and thymol and/or terpineol
  • compositions as per the invention (Examples 3,4,6,7,9,10) provide for vastly superior antibacterial efficacy as compared to compositions outside the invention (Examples 1,2,5,8).
  • compositions of the invention are effective even at short contact times of about 30 seconds.
  • compositions as shown in Table - 4 were tested for
  • Example 15 to 19 give vastly superior antibacterial efficacy as compared to a sample outside the invention (Example 14) .

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)
  • Health & Medical Sciences (AREA)
  • Emergency Medicine (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)
  • Detergent Compositions (AREA)

Abstract

L'invention porte sur une composition liquide de nettoyage et désinfection de surfaces dures. Les présents inventeurs ont trouvé que l'incorporation de chlorure de benzalkonium et de sels choisis d'acide dicarboxylique ou tricarboxylique, lorsqu'ils sont combinés à du thymol ou du terpinéol, assure un effet antimicrobien synergétique d'une manière rapide et qu'une telle efficacité est obtenue à de très faibles concentrations en thymol et/ou en terpinéol.
EP12769078.2A 2011-11-03 2012-09-26 Composition liquide de nettoyage antimicrobien de surfaces dures Active EP2773739B1 (fr)

Priority Applications (1)

Application Number Priority Date Filing Date Title
PL12769078T PL2773739T3 (pl) 2011-11-03 2012-09-26 Ciekłe przeciwmikrobowe kompozycje czyszczące do twardych powierzchni

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
IN3095MU2011 2011-11-03
PCT/EP2012/068987 WO2013064315A1 (fr) 2011-11-03 2012-09-26 Composition liquide de nettoyage antimicrobien de surfaces dures

Publications (2)

Publication Number Publication Date
EP2773739A1 true EP2773739A1 (fr) 2014-09-10
EP2773739B1 EP2773739B1 (fr) 2015-11-04

Family

ID=46980938

Family Applications (1)

Application Number Title Priority Date Filing Date
EP12769078.2A Active EP2773739B1 (fr) 2011-11-03 2012-09-26 Composition liquide de nettoyage antimicrobien de surfaces dures

Country Status (7)

Country Link
EP (1) EP2773739B1 (fr)
CN (1) CN103890160B (fr)
BR (1) BR112014008053B1 (fr)
EA (1) EA022049B1 (fr)
MX (1) MX339345B (fr)
PL (1) PL2773739T3 (fr)
WO (1) WO2013064315A1 (fr)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN106318653A (zh) * 2016-08-19 2017-01-11 桂林福冈新材料有限公司 一种清洗后无痕迹的玻璃洗涤剂

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US9206381B2 (en) 2011-09-21 2015-12-08 Ecolab Usa Inc. Reduced misting alkaline cleaners using elongational viscosity modifiers
US9309485B2 (en) 2013-06-26 2016-04-12 Ecolab USA, Inc. Use of nonionics as rheology modifiers in liquid cleaning solutions
WO2015021301A1 (fr) * 2013-08-07 2015-02-12 Giovanniello Joseph Compositions de désinfectant antimicrobien et leurs méthodes de fabrication
US9637708B2 (en) 2014-02-14 2017-05-02 Ecolab Usa Inc. Reduced misting and clinging chlorine-based hard surface cleaner
WO2017089104A1 (fr) * 2015-11-27 2017-06-01 Unilever N.V. Composition antimicrobienne
CN109153944A (zh) 2016-05-19 2019-01-04 埃科莱布美国股份有限公司 用于与基于方解石的石材一起使用的清洁组合物
US10392587B2 (en) 2016-05-23 2019-08-27 Ecolab Usa Inc. Reduced misting alkaline and neutral cleaning, sanitizing, and disinfecting compositions via the use of high molecular weight water-in-oil emulsion polymers
MX2018013936A (es) 2016-05-23 2019-03-28 Ecolab Usa Inc Composiciones acidas de limpieza, sanitizacion y desinfeccion con nebulizacion reducida a traves del uso de polimeros de emulsion de agua en aceite de alto peso molecular.
AU2018227539B2 (en) 2017-03-01 2020-04-09 Ecolab Usa Inc. Reduced inhalation hazard sanitizers and disinfectants via high molecular weight polymers
DE102017124010A1 (de) * 2017-10-16 2019-04-18 Oliver Ganzenmüller Stoffgemisch zur Reinigung von Oberflächen
JP7170300B2 (ja) * 2017-12-11 2022-11-14 株式会社ニイタカ 液体洗浄剤組成物
MX2022000454A (es) 2019-07-12 2022-04-18 Ecolab Usa Inc Limpiador alcalino de niebla reducida mediante el uso de polímeros en emulsión solubles en álcali.
RU2766860C1 (ru) * 2021-04-26 2022-03-16 Общество с ограниченной ответственностью «Синергия Технологий» Моющая композиция
AR126534A1 (es) 2021-08-04 2023-10-18 Unilever Global Ip Ltd Una composición blanqueadora estable
AR126535A1 (es) 2021-08-04 2023-10-18 Unilever Global Ip Ltd Una composición blanqueadora antimicrobiana

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CN106318653A (zh) * 2016-08-19 2017-01-11 桂林福冈新材料有限公司 一种清洗后无痕迹的玻璃洗涤剂

Also Published As

Publication number Publication date
MX339345B (es) 2016-05-20
CN103890160B (zh) 2017-03-08
EA201400533A1 (ru) 2014-08-29
EA022049B1 (ru) 2015-10-30
BR112014008053A2 (pt) 2017-04-11
CN103890160A (zh) 2014-06-25
WO2013064315A1 (fr) 2013-05-10
EP2773739B1 (fr) 2015-11-04
MX2014005403A (es) 2014-07-11
PL2773739T3 (pl) 2016-06-30
BR112014008053B1 (pt) 2021-06-01

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