AUSTRALIA Patents Act COMPLETE SPECIFICATION (ORIGINAL) Class Int. Class Application Number: Lodged: Complete Specification Lodged: Accepted: Published: Priority Related Art: Name of Applicant: Rohm and Haas Company Actual Inventor(s): John William Ashmore, Li-Liang Chia, Beverly Jean Ei A'mma Address for Service and Correspondence: PHILLIPS ORMONDE FITZPATRICK Patent and Trade Mark Attorneys 367 Collins Street Melbourne 3000 AUSTRALIA Invention Title: ANTIMICROBIAL COMPOSITION USEFUL FOR PRESERVING WOOD Our Ref: 916923 POF Code: 496570/83886 The following statement is a full description of this invention, including the best method of performing it known to applicant(s): -1 - Ia The present application is a divisional application from Australian Patent Application No. 2006202280, which claims priority from United States Provisional Application No. 60/690,685 filed 15 June 2005, which is incorporated herein by reference in its entirety. This invention relates to combinations of biocides useful for preserving wood, the 5 combinations having greater activity than would be observed for the individual antimicrobial compounds. Use of combinations of at least two antimicrobial compounds can broaden potential markets, reduce use concentrations and costs, and reduce waste. In some cases, commercial antimicrobial compounds cannot provide effective control of microorganisms, even at high use 10 concentrations, due to weak activity against certain types of microorganisms, e.g., those resistant to some antimicrobial compounds. Combinations of different antimicrobial compounds are sometimes used to provide overall control of microorganisms in a particular end use environment. For example, U.S. Pat. No. 5,591,760 discloses a synergistic combination of 4,5-dichloro-2-n-octyl-4-isothiazolin-3-one and a number of other biocides, 15 including 3-iodo-2-propynyl-butylcarbamate, but this reference does not suggest any of the combinations claimed herein. Moreover, there is a need for additional combinations of antimicrobial compounds having enhanced activity against various strains of microorganisms to provide effective control of the microorganisms that is both quick and long lasting. The problem addressed by this invention is to provide such additional combinations of 20 antimicrobial compounds. STATEMENT OF THE INVENTION The present invention is directed to a synergistic antimicrobial composition comprising: (a) tebuconazole, and (b) a mixture of 5-chloro-2-methyl -4-isothiazolin-3 -one 25 and 2-methyl-4-isothiazolin-3-one. DETAILED DESCRIPTION OF THE INVENTION "M" is 2-niethyl-4-isothiazolin-3-one, also referred to by the name 2 methyl-3-isothiazolone. "CMI" is 5chlor-2-methyl-isothiazlin-3-one. "DCOIT" is 4,5-dichloro-2-n-oc(tyl-4-isohinzolin -3-one. "OIT" is 2-n-octyl-4 isothiazolin-3-one. "IPBC" is 3-iodo-2-propyiyl-butylcarbamate. Copper 2 tebuconazole is a biocide formulation containing a monoethanolamine complex of copper oxide and tebuconazole. A "copper alkyldimethylammonium salt" is a biocide formulation containing a monoethanolamine complex of copper oxide and an 5 alkyldimethylammonium salt. In one embodiment, the alkyldimethylammonium salt is alkylbenzyldimethylammonium salt. In another embodiment, the alkyldimethylammonium salt is dialkyldimethylammonium salt. In another embodiment, the alkyldimethylammonium salt is an aryloxyethoxyethyl dimethyl benzylammonium salt, wherein aryl preferably is diisobutylphenyl or 10 diisobutyleresyl. Preferably the salt is a chloride, carbonate or bicarbonate. Preferably, the weight ratio of copper oxide to alkyldimethylammonium salt is from 30:70 to 80:20. In one embodiment, the ratio of copper oxide to alkyldimethylammonium salt is. from 55:45 to 80:20, more preferably from 62:38 to 71:29. In another embodiment, the ratio is from 35:65 to 65:35, more 15 preferably from 46:55 to 55:45, Preferably the alkyl groups are in the range from Ca-Cis, with the majority being Cs-C14. In one embodiment, the alkyl groups are. 67% C 12 , 25% C, 7% C16 and 1% Ci. In another embodiment, the alkyl group are from C8-Ci 2 . As used herein, the following terms have the designated definitions, 20 unless the context clearly indicates otherwise. The term " antimicrobial compound" refers to a compound capable of inhibiting the growth of or controlling the growth of microorganisms at a locus; antimicrobial compounds include bactericides, bacteristats, fungicides, fungistats, algaecides and algistats, depending on the dose level applied, system conditions and the level of microbial 25 control desired. The term "microorganism" includes, for example, fungi (such as yeast and mold), bacteria and algae. The term "locus" refers to an industrial system or product subject to contamination by microorganisms. The following abbreviations are used throughout the specification: ppm= parts per million by weight (weight/weight), mL = milliliter, ATCC = American Type Culture 30 Collection, and MIC = minimum inhibitory concentrAtion. Unless otherwise specified, temperatures are in degrees centigrade (0), and references to percentages (%) are by weight. Percentages of antimicrobial compounds in the 3 composition of this invention are based on the total weight of active ingredients in the composition, i.e., the antimicrobial compounds themselves, exclusive of any amounts of solvents, carriers, dispersants, stabilizers or other materials which may be present. "Salt-free" means that the composition contains zero or up to 0.6%, preferably zero or up to 0.1%, and more preferably zero or up to 0.01%, of metal salt, based on weight of the composition. In another embodiment of the invention, the antimicrobial composition comprises tebuconazole and a mixture of 5-chloro-2-methyl-4-isothiazolin-3-one and 2-methyl-4 isothiazolin-3-one. Preferably, a weight ratio of tebuconazole to a mixture of 5-chloro-2 5 methyl-4-isothiazolin-3-one and 2-methyl-4-isothiazolin-3-one is from 1/0.001 to 1/0.15. The antimicrobial compounds in the composition of this invention may be used "as is" or may first be formulated with a solvent or a solid carrier. Suitable solvents include, for example, water; glycol, such as ethylene glycol, propylene glycol, diethylene glycol, dipropylene glycol, polyethylene glycol, and polypropylene glycol, glycol ethers; alcohols, such as methanol, ethanol, propanol, phenethyl alcohol and phenoxypropanol; ketones, such as acetone and methyl ethyl ketone; esters, such as ethyl acetate, butyl acetate, glycerol triacetate, TEXANOL (2,2,4-trimethyl- 1,3-pentanediol, mono-isobutyrate ester; available from Eastman Co., Kingsport TN), and methyl and isobutyl esters of Cr C7 dicarboxylic acids. e.g.. succinic, glutaric and adipic acids; carbonates, such as propylene carbonate and dimethyl carbonate; and mixtures thereof. It is preferred that the solvent is selected from water, glycols, glycol ethers, esters and mixtures thereo. Suitable solid carriers include, for example, cyclodextrin, silicas, diatomaceous earth, waxes, cellulosic materials, alkali and alkaline earth (e.g., sodium, magnesium, potassium) metal salts (e.g., chloride, nitrate, bromide, sulfate) and charcoal.
4 When an antimicrobial component is formulated in a solvent, the formulation may optionally contain surfactants. When such formulations contain surfactants, they are generally in the form of emulsive concentrates, emulsions, microemulsive concentrates, or microemulsions. Emulsive 5 concentrates form emulsions upon the addition of a sufficient amount of water. Microemulsive concentrates form microemulsions upon the addition of a sufficient amount of water. Such emulsive and microemulsive concentrates are generally well known in the art. U.S. Patent No. 5,444,078 may be consulted for further general and specific details on the preparation of various microemulsions 10 and microemulsive concentrates. An antimicrobial compound also can be formulated in the form of a dispersion. The solvent component of the dispersion can be an organic solvent or water, preferably water. Such dispersions can contain adjuvants, for example, co-solvents, thickeners, anti-freeze agents, dispersants, fillers, pigments, 15 surfactants, biodispersants, sulfosuccinates, terpenes, furanones, polycations, stabilizers, scale inhibitors and anti-corrosion additives. The antimicrobial compounds may be formulated separately or together. When both antimicrobial compounds are each first formulated with a solvent, the solvent used for the first antimicrobial compound may be the same as or different 20 from the solvent used to formulate the other commercial antimicrobial compound. It is preferred that the two solvents are miscible. In the alternative, the first antimicrobial compound and the other antimicrobial compound may be combined directly and then a solvent added to the mixture. Those skilled in the art will recognize that the antimicrobial compounds of 25 the present invention may be added to a locus sequentially, simultaneously, or may be combined before being added to the locus. It is preferred that the first antimicrobial compound and the second antimicrobial compound be added to a locus simultaneously or combined prior to being added to the locus. When the antimicrobial compounds are combined prior to being added to a locus, such 30 combination may optionally contain adjuvants, such as, for example, solvent, thickeners, anti-freeze agents, colorants, sequestrants (such as ethylenediamine tetraacetic acid, ethylenediaminedisuccinic acid, iminodisuccinic acid and salts 5 thereof), dispersants, surfactants, biodispersants, sulfosuccinates, terpenes, furanones, polycations, stabilizers, scale inhibitors and anti-corrosion additives. The antimicrobial compositions of the present invention can be used to inhibit the growth of microorganisms by introducing an antimicrobially effective 5 amount of the compositions onto, into, or at a locus subject to microbial attack. Suitable loci include, for example: cooling towers; air washers; mineral slurries; wastewater treatment; ornamental fountains; reverse osmosis filtration; ultrafiltration; ballast water; evaporative condensers; heat exchangers; pulp and paper processing fluids; plastics; emulsions; dispersions; paints; latices; coatings, 10 such as varnishes; construction products, such as mastics, caulks, and sealants; construction adhesives, such as ceramic adhesives, carpet backing adhesives, and laminating adhesives; industrial or consumer adhesives; photographic chemicals; printing fluids; household products, such as bathroom and kitchen cleaners; cosmetics; toiletries; shampoos; soaps; detergents; industrial cleaners; floor 15 polishes; laundry rinse water; metalworking fluids; conveyor lubricants; hydraulic fluids; leather and leather products; textiles; textile products; wood and wood products, such as plywood, chipboard, flakeboard, laminated beams, oriented strandboard, hardboard, and particleboard; petroleum processing fluids; fuel; oilfield fluids, such as injection water, fracture fluids, and drilling muds; 20 agriculture adjuvant preservation; surfactant preservation; medical devices; diagnostic reagent preservation; food preservation, such as plastic or paper food wrap; pools; and spas. Preferably, the antimicrobial compositions of the present invention are used to inhibit the growth of microorganisms at a locus selected from one or more 25 of wood and wood products, emulsions, dispersions, paints, latices, household products, cosmetics, toiletries, shampoos, soaps, detergents, machining fluids and industrial cleaners. In particular, the antimicrobial compositions are useful in wood and wood products, emulsions, dispersions, paints and latices. When the synergistic compositions of the present invention are used in 30 personal care compositions, the formulated compositions may also comprise one or more ingredients selected from UV radiation-absorbing agents, surfactants, rheology modifiers or thickeners, fragrances, moisturizers, humectants, 6 emollients, conditioning agents, emulsifiers, antistatic aids, pigments, dyes, tints, colorants, antioxidants, reducing agents and oxidizing agents. The specific amount of the composition of this invention necessary to inhibit or control the growth of microorganisms in a locus depends upon the 5 particular locus to be protected. Typically, the amount of the composition of the present invention to control the growth of microorganisms in a locus is sufficient if it provides from 0.1 to 25,000 ppm active ingredient of the composition in the locus. It is preferred that the active ingredients of the composition be present in the locus in an amount of at least 0.5 ppm, more preferably at least 1 ppm, more 10 preferably at least 10 ppm and most preferably at least 50 ppm. In one embodiment of the invention, the active ingredients are present in an amount of at least 500 ppm. It is preferred that the active ingredients of the composition be present in the locus in an amount of no more than 20,000 ppm, more preferably no more than 15,000 ppm, more preferably no more than 1000 ppm. In one 15 embodiment of the invention, the active ingredients are present in an amount of no more than 10,000 ppm, more preferably no more than 5,000 ppm, and most preferably no more than 1,000 ppm.
7 EXAMPLES The synergism of the combination of the present invention was demonstrated by testing a wide range of concentrations and ratios of the compounds. 5 One measure of synergism is the industrially accepted method described by Kull, F.C.; Eisman, P.C.; Sylwestrowicz, H.D. and Mayer, R.L., in Applied Microbiology 9:538-641 (1961), using the ratio determined by the formula: Ca/CA + Cb/CB = Synergy Index ("SI") 10 wherein: CA = concentration of compound A (first component) in ppm, acting alone, which produced an end point (MIC of Compound A). Ca = concentration of compound A in ppm, in the mixture, which produced an end point. 15 CB = concentration of compound B (second component) in ppm, acting alone, which produced an end point (MIC of Compound B). Ch = concentration of compound B in ppm, in the mixture, which produced an end point. 20 When the sum of Ca/CA and Cb/CB is greater than one, antagonism is indicated. When the sum is equal to one, additivity is indicated, and when less than one, synergism is demonstrated. The lower the SI, the greater the synergy shown by that particular mixture. The minimum inhibitory concentration (MIC) of an antimicrobial compound is the lowest concentration tested under a specific 25 set of conditions that prevents the growth of added microorganisms. Synergy tests were conducted using standard microtiter plate assays with media designed for optimal growth of the test microorganism. Minimal salt medium supplemented with 0.2% glucose and 0.1% yeast extract (M9GY medium) was used for bacteria testing; Potato Dextrose Broth (PDB medium) 30 was used for yeast and mold testing. In this method, a wide range of combinations of microbicides was tested by conducting high resolution MIC assays in the presence of various concentrations of biocides. High resolution 8 MICs were determined by adding varying amounts of microbicide to one column of a microtitre plate and doing subsequent ten-fold dilutions using an automated liquid handling system to obtain a series of end points ranging of active ingredient. The synergy of the combinations of the present invention was 5 determined against two bacteria, Pseudomonas aeruginosa (Ps. aeruginosa - ATCC # 9027) and Staphylococcus aureus (S. aureus - - ATCC # 6538), a yeast, Candida albicans (C. albicans - ATCC # 10231), and a mold, Aspergillus niger (A. niger -- ATCC 16404). The bacteria were used at a concentration of about 1 6 x 106 bacteria per mL and the yeast and mold at 1-5 x 105 fungi per mL. These 10 microorganisms are representative of natural contaminants in many consumer and industrial applications. The plates were visually evaluated for microbial growth (turbidity) to determine the MIC after various incubation times at 250C (yeast and mold) or 300C (bacteria). The test results for demonstration of synergy of the microbicide 15 combinations of the present invention are shown below in the Tables. Each table shows the specific combinations of Component (a) and the second component (b); results against the microorganisms tested with incubation times; the end-point activity in ppm measured by the MIC for Component (a) (Ca), for the second component alone (C), for the mixture (Ca) and for second component in the 20 mixture (Cb); the calculated SI value; and the range of synergistic ratios for each combination tested (first component/second component or a+b). An application test was performed to evaluate synergy of DCOIT/ thifluzamide alone and in combination against Gloeophyllum trabeum (G. trabeum - ATCC # 11593) and Trametes vesicolor (T. vesicolor - - ATCC # 4262). 25 A paper disc was dipped in the treatment solution, air dried and placed on Malt agar plate streaked with the test organisms. The surface of the disc was also swabbed with the test organisms. The agar plates were incubated at 25'C for 4 weeks. Fungal growth was then observed visually. The following Tables summarize data for combinations of biocides against fungi and bacteria, along with their synergy index (SI) and the weight ratios of biocides. All amounts of biocides are reported as ppm of active ingredient.
9 Ca = Component A (DCOIT) Cb = Component B (MD Ratio = Ca/Cb Test Organisms Contact Time Ca Cb S.I. Ca/Cb Ps. Aeruginosa 24 hour 3.2 ATCC# 9027 20 0.7 15 0.97 1/21.5 48 hour 5.3 - - 20 3.9 5 0.99 1/1.3 2.6 10 0.99 1/3.8 1.8 10 0.84 1/5.6 1.2 15 0.98 1/12.5 1.8 15 1.09 1/8.3 3.2 10 1.1 1/3.1 Saureus 24hour 0.1 ATCC#6538 - 3 0.04 20 1.07 0 48 hour 0.4 40 0.1 25 0.88 1/250 0.04 30 0.85 1/750 0.06 30 0.9 1/500 0.1 30 1 1/300 A. niger 3 days 1 ATCC# 16404 450 0.55 200 0.99 2/727 0.44 250 1 1/568 0.26 300 0.93 1/1153 0.33 300 1 1/909 0.26 350 1.04 1/1346 7 days 1 450 1 0.3 300 0.971 1/1000 10 Ca = Component A (ACQ-C)' Cb = Component B (copper 8-hydroxyquinoline) Ratio = Ca/Cb Test Organisms Contact Time Ca Ch S.I. Ca/Cb S.aureu. 48hour 2 ATCC#6538 3 0.53 1 0.6 1/2 0.65 1 0.66 1/1.5 0.88 1 0.77 1/1.4 1.1 1 0.88 1/0.9 0.53 2 0.93 1/4 0.65 2 0.99 1/3 0.88 2 1.11 1/2.3 A. niger 3 days 32 - ATCC# 16404 7 6.6 5 0.92 1/0.8 7 days 32 - .. 8 - 6.6 6 0.96 1/0.9 C. albicans 24 hour 4.6 - ATCC# 10231 15 2.1 5 0.79 1/2.4 3 5 0.99 1/1.7 0.8 10 0.84 1/12.5 1.4 10 0.97 1/7.1 48 hour 6.1 - - 20 - 2.1 5 0.59 1/2.4 3 5 0.74 1/1.7 4.6 5 1 1/1.1 1_ 1_ 1.4 15 0.98 1/10.7 1. "ACQ-C" is a formulation of copper oxide monoethanolamine complex with alkyl benzy1dimethylammonium chloride, wherein the alkyl group is a mixture of 5 C-Ci alkyls, with the majority being C 12 and C4, and the weight ratio of copper oxide to alkyl benzyldimethylammonium chloride is from 62:38 to 71:29.
11 Ca = Component A (copper 8-hydroxyquinoline) Cb = Component B (OIT) Ratio = Ca/Cb Test Organisms Contact Time Ca Cb S.I. Ca/Cb Ps. Aeruginosa 48 hour 7 ATCC# 9027 - 415 3 180 0.86 1/60 3 255 1.04 1/85 S.aureus 24hour 3 ATCC#6538 63 1 36 0.9 1/36 2 13.2 0.88 1/6.6 2 24 1.05 1/12 48hour 4 - 78 1 51 0.9 1/51 1 63 1.06 1/63 2 36 0.96 1/18 13 13.2 0.92 1/4.4 C. albicans 24 hour 15 ATCC# 10231 0.6 5 0.33 0.88 1/0.06 10 0.09 0.82 1/0.01 10 0.13 0.88 1/0.01 10 0.16 0.93 1/0.02 10 0.2 1. 1/0.02 48 hour 15 - - 0.9 10 0.2 0.89 1/0.02 10 0.26 0.96 1/0.03 1 1 1 5 0.6 1 1/0.02i 12 Ca = Component A (ACQ-C) Cb = Component B (OIT) Ratio = Ca/Cb Test Organisms Contact Time Ca Cb S.I. Ca/Cb Pa. Aeruginosa 24 hour 20 ATCC# 9027 - 390 5 315 1.06 1/63 15 129 1.06 1/8.6 48 hour 20 - 525 10 256 0.99 1/25.5 15 180 1.09 1/12 S.aureus 24 hour I ATCC#6538 63 0.4 24 0.78 1/60 0.6 24 0.98 1/40 0.4 36 0.97 1/90 0.6 10.6 0.77 1/17.5 0.8 10.5 0.97 1/13.1 48hour 2 78 0.8 51 1.05 1/63.8 C. albicans 24 hour 8 ATCC# 10231 0.6 2 0.3 0.75 1/0.15 4 0.3 1 1/0.08 48hour 8 0.9 2 0.6 0.92 1/0.3 A. niger 3 days 30 ATC# 16404 - 3.3 5 1 0.47 1/0.2 5 1.5 0.62 1/0.3 5 2.1 0.8 1/0.4 5 2.6 0.95 1/0.5 10 0.33 0.43 1/0.03 10 0.44 0.47 1/0.04 10 0.56 0.5 1/0.06 10 1 0.64 1/0.1 20 0.33 0.77 1/0.017 7 daya 30 - 3.3 10 1 0.64 1/0.1 10 1.5 0.79 1/0.15 10 2.1 0.97 1/0.21 1_ 1_20, 1 0.97 1/0.05 13 Ca = Component A (copper 8-hydroxyquinoline) Cb = Component B (IPBC) Ratio = Ca/Cb Test Organisms Contact Time Ca Cb S.I. Ca/Cb Ps. Aeruginosa 24 hour 7 ATCC #9027 - 263 2 195 1.03 1/97.5 3 158 1.03 1/52.7 4 60 0.8 1/15 4 90 0.91 1/22.5 5 60 0.94 1/12 48hour 7 - 263 3 128 0.92 1/42.7 3 158 1.03 1/52.7 4 128 1.06 1/32 S.aureus 24 hour 3 ATCC# 6538 - 34 1 8.8 0.59 1/8.8 1 16 0.8 1/16 2 24 1.04 1/24 2 8.8 0.93 1/4.4 2 4.2 0.79 1/2.1 2 5.2 0.82 1/2.6 2 7 0.87 1/3.5 2 8.8 0.93 1/4.4 48hour 3 42 1 8.8 0.54 1/8.8 1 16 0.71 1/16 1 24 0.9 1/24 2 8.8 0.88 1/4.4 2 5 0.77 1/2.5 2 16 1.05 1/8 2 5.2 0.79 1/2.6 2 7 0.83 1/3.5 2 5.2 0.79 1/2.6 2 8.8 0.88 1/4.4 C. albicans 24 hour 15 ATCC # 10231 - 4.2 5 1.6 0.71 1/0.32 5 2.4 0.9 1/0.48 10 1.6 1.05 1/1.6 48 hour 15 4.2 I__ _ 1___ 5 2.4 0.9 1/0.48 14 Ca = Component A (DCOIT) Cb = Component B (Cu-tebuconazole complex) Ratio = Ca/Cb Test Organisme Contact Time Ca Cb S.I. Ca/Cb Ps. Aeruginosa 24 hour 3.2 ATCC#9027 150 1.8 25 0.73 1/13.9 0.32 100 0.77 1/313 0.39 100 0.79 11256 0.66 100 0.87 1/152 1.2 100 1.04 1/83 48 hour 5.3 - - 200 1.8 25 0.46 1/13.9 3.2 25 0.73 1/7.8 3.9 25 0.86 1/6.4 1.8 50 0.69 1/27.8 1.8 100 0.84 1/55.6 1.8 150 1.09 1/83.3 0.39 100 0.57 1/256.4 0.66 100 0.62 1/151.5 1.2 100 0.73 1/83.3 1.8 100 0.84 1/56.6 0.53 150 0.85 1/283 1.2 100 0.73 1/83.3 ..- 1.8 100 0.84 1/55.6 S. aureus 24 hour 0.1 - 40 0.02 35 0.79 1/1750 A. niger 3 days 1.5 - - ATCC# 16404 - 80 - 0.44 40 0.79 1/90.9 0.55 40 0.87 1/72.7 0.44 50 0.92 1/113.6 0.4 60 1.04 1/150 0.33 60 0.97 1/181.8 7 days 2.1 - 80 0.55 40 0.76 1/72.7 1 40 0.98 1/40 0.55 50 0.89 1/90.9 0.55 60 1.01 1/109 1___ _ 10.5 50 0.88 1/100 15 Ca Component A (copper 8-hydroxyquinoline) Cb = Component B (Cu-tebuconazole complex) Ratio = Ca/Cb Test OrganiEsma Contact Time Ca Cb S.I. Ca/Cb Pa. aureginosa 24 hour 7 ATCC # 9027 - 195 4 60 0.88 1/16 5 60 1.02 1/12 S. aureus 24 hour 4 - ATCC# 6538 44 2 21 0.98 1/10.5 48hour 4 - 44 1 26 0.84 1/26 1 33 1 1/33 1___ 12 26 1.09 1/13 Ca =.Component A (copper 8 hydroxyquinoline) Ch = Component B (DCOIT) Ratio.= Ca/Cb Test Organisms Contact Time Ca Cb S.I. Ca/Cb Pa. aureginosa 24 hour .7 - ATCC#9027 3.2 3 1.8 1 1/0.6 48 hour 7 - 5.3 - 2 3.9 1.02 1/2 S. aureus 24 hour 3 ATCC # 6538 - 0.1 2 0.01 0.8 1/0.005 1 0.03 0.6 1/0.03 1 2 0.03 1 1/0.015 16 Ca = Component A (tebuconazole) Cb = Component B (copper 8-hydroxyquinoline) Ratio = Ca/Cb Test Organisms Contact Time Ca Cb S.I. Ca/Cb Pa. Aeruginoaa 24 hour 900 ATCC#9027 - 7 200 2 1.06 1/0.01 S. aureus 24 hour 50 - 3.3 40 0.3 0.89 1/0.008 30 0.4 0.72 1/0.01 20 0.4 0.52 1/0.02 50 0.3 1.09 1/0.06 40 0.4 0.92 1/0.01 48 hour 60 - 4.4 40 0.6 0.94 1/0.015 30 1 0.83 1/0.033 20 1 0.63 1/0.05 --....- 40 L .. 03 1/0.025 17 C. albicans 24 hour 60 ATCC # 10231 15.8 50 0.3 0.85 1/0.006 50 0.6 0.87 1/0.012 50 1.3 0.92 1/0.026 50 1.6 0.93 1/0.032 50 2 0.96 1/0.04 50 2.6 1 1/0.052 50 3.3 1.04 1/0.066 40 0.3 0.69 1/0.008 4D 0.6 0.7 1/0.015 40 0.9 0.72 1/0.023 40 1.3 0.75 1/0.033 40 1.6 0.77 1/0.04 40 2 0.79 1/0.05 40 2.6 0.83 1/0.065 40 3.3 0.88 1/0.083 40 6 1.05 1/0.15 30 0.6 0.54 1/0.02 30 0.9 0.56 1/0.03 30 1.3 0.58 1/0.043 30 1.6 0.6 1/0.063 30 2 0.63 1/0.067 30 2.6 0.66 1/0.087 30 3.3 0.71 1/0.11 30 6 0.88 1/0.2 30 9 1.07 1/0.3 20 1.3 0.42 1/0.065 20 1.6 0.43 1/0.08 20 2 0.46 1/0.1 20 2.6 0.5 1/0.13 20 3.3 0.54 1/0.165 20 6 0.71 1/0.3 20 9 0.9 1/0.45 10 3.3 0.38 1/0.33 10 6 0.54 1/0.6 10 9 0.74 1/0.9 10 12.8 0.98 1/1.28 18 48 hour 60 19.5 50 0.6 0.86 1/0.012 50 0.9 0.88 1/0.018 50 1.3 0.9 1/0.026 50 1.6 0.92 1/0.032 60 2 0.94 1/0.04 50 2.6 0.97 1/0.052 50 3.3 1 1/0.066 40 0.6 0.7 1/0.015 40 0.9 0.71 1/0.023 40 1.3 0.73 1/0.033 40 1.6 0.75 1/0.04 40 2 0.77 1/0.05 40 2.6 0.8 1/0.066 40 3.3 0.84 1/0.083 40 6 0.97 1/0.15 30 2 0.6 1/0.067 30 2.6 0.63 1/0.087 30 3.3 0.67 1/0.11 30 6 0.81 1/0.2 30 9 0.96 1/0.3 20 3.3 0.5 1/0.165 20 6 0.64 1/0.3 20 9 0.79 1/0.45 20 12.8 0.99 1/0.64 10 6 0.47' 110.6 10 9 0.63- 1/0.9 10 12.8 0.82 1/1.28 10 '15.8 0.98 1/1.58 19 A. niger 3 days 8 ATCC # 16404 6 7 0.36 0.94 1/0.05 7 0.51 0.96 1/0.07 7 0.63 0.98 1/0.09 7 0.78 1.01 1/0.11 6 0.36 0.81 1/0.06 6 0.51 0.84 1/0.085 6 0.63 0.86 1/0.105 6 0.78 0.88 1/0.13 6 1.05 0.93 1/0.175 6 1.32 0.97 1/0.22 6 2 1.08 1/0.33 5 0.78 0.76 1/0.156 5 1.05 0.8 1/0.21 5 1.32 0.85 1/0.264 5 2 0.96 1/0.4 4 0.78 0.63 1/0.195 4 1.05 0.68 1/0.263 4 1.32 0.72 1/0.33 4 2 0.83 1/0.5 3 2 0.71 1/0.67 3 4 1.04 1/1.33 2 2 0.58 1/1 2 4 0.92 1/2 7 days 8 6 7 0.36 0.94 1/0.051 7 0.51 0.96 1/0.073 7 0.63 0.98 1/0.09 7 0.78 1.01 1/0.11 6 0.36 0.81- 1/0.06 6 0.51 0.84 1/0.085 6 0.63 0.86 1/0.105 6 0.78 0.88 1/0.13 6 1.05 0.93 1/0.175 6 1.32 0.97 1/0.22 5 0.78 0.755 1/0,156 5 1.05 0.8 1/0.21 5 1.32 0.845 1/0.264 5 2 0.96 1/0.4 4 0.78 0.63 1/0.195 4 1.05 0.68 1/0.263 4 1.32 0.72 1/0.33 4 2 0.83 1/0.5 3 2 0.71 1/0.67 3 4 1.04 1/1.33 _____ _ _ _ 1 2 1 4 0.92 1/2 20 Ca = Component A (tebuconazole) Cb = Component B (DCOIT) Ratio = Ca/Cb Table 10 Test Organisms Contact Time Ca Cb S.I. Ca/Cb Ps. Aeruginosa 48 hour 900 ATCC#9027 - 3.9 50 2.6 0.72 1/0.052 100 2.6 0.78 1/0.026 200 2.6 0.89 1/0.013 300 1.8 0.79. 1/0.006 400 1.8 0.91 1/0.005 500 1.8 1.02 1/0.004 S.aureus 24hour 50 - 0.2 40 0.01 0.85 1/0.0003 30 0.02 0.7 1/0.0007 40 0.02 0.9 1/0.0005 40 0.03 0.95 1/0.0008 40 0.04 1 1/0.001 48 hour 50 0.3 40 0.04 0.93 1/0.001 30 0.1 0.93 1/0,003 A. niger 3 days 8 ATCC # 16404 1.8 6 0.32 0.93 1/0.053 6 0.39 0.97 1/0.065 5 0.32 0.8 1/0.064 5 0.39 0.84- 1/0.078 5 0.53 0.92 1/0.106 5 0.66 0.99 1/0.132 4 0.32 0.68 1/0.08 4 0.39 0.72 1/0.098 4 0.63 0.79 1/0.133 4 0.66 0.87 1/0.165 3 0.39 0.59 1/0.13 3 0.53 0.67 1/0.177 3 0.66 0.74 1/0.22 3 1.2 1.04 1/0.4 2 1.2 0.92 1/0.6 21 7days 8 3.2 7 0.32 0.98 1/0.046 6 0.39 0.87 1/0.065 6 0.53 0.92 1/0.088 6 0.66 0.96 1/0.11 5 0.53 0.79 1/0.106 5 0.39 0.75 1/0.078 5 0.53 0.79 1/0.106 5 0.66 0.83 1/0.132 4 0.53 0.67 1/0.133 4 0.66 0.71 1/0.165 1_ 1_ _ 4 1.2 0.88 1/0.3 Ca = Component A (tebuconazole) Cb = Component B (OIT) Ratio = Ca/Cb Test Organisms Contact Time Ca Cb S.I. Ca/Cb Pa. Aeruginosa 24 hour 900 ATCC # 9027 390 800 66 1.06 1/0.083 700 120 1.09 1/0.17 600 120 0.97 1/0.2 500 120 0.86 1/0.24 48 hour 900 390 500 180 1.02 1/0.36 S. aureus 24 hour 50 63 10 51 1.01 1/5.1 C. albicans 24 hour 50 ATCC# 10231 0.9 40 0.02 0.82 1/0.005 40 0.026 0.83 1/0.0007 40 0.033 0.84 1/0.0008 40 0.06 0.87 1/0.015 40 0.09 0.90 1/0.0023 40 0.13 0.94 1/0.0033 40 0.16 0.98 1/0.004 30 0.06 0.67 1/0.002 30 0.09 0.70 1/0.003 30 0.13 0.74 1/0.004 30 0.16 0.78 1/0.005 30 0.2 0.82 1/0.0067 30 0.26 0.89 1/0.0087 30 0.33 0.97 1/0.011 1 20 0.33 0.77 1/0.0165 22 Ca = Component A (tebuconazole) Cb = Component B (CMIT/MIT) Ratio = Ca/Cb Test Organisms Contact Time Ca Cb S.I. Ca/Cb S. aureus 24 hour 50 40 0.04 0.84 1/0.001 30 0.06 0.66 1/0.002 20 0.1 0.5 1/0.005 10 0.27 0.47 1/0.027 10 0.33 0.53 1/0.033 10 0.44 0.64 1/0.044 10 0.55 0.75 1/0.055 20 0.15 0.56 1/0.008 20 0.21 0.61 1/0.011 20 0.26 0.66 1/0.013 20 0.32 0.72 1/0.016 20 0.44 0.84 1/0.022 20 0.55 0.95 1/0.028 20 0.21 0.61 1/0.011 30 0.1 0.7 1/0.003 30 0.15 0.76 1/0.005 30 0.21 0.81 1/0.007 30 0.26 0.86 1/0.008 30 0.32 0.92 1/0.011 30 0.44 1.04 1/0.015 40 0.06 0.86 1/0.002 40 0.1 0.9 1/0.003 40 0.15 0.95 1/0.004 40 0.21 1.01 1/0.005 40 0.26 1.06 1/0.007 48hour 50 - 3 40 0.1 0.83 1/0.003 40 0.15 0.85 1/0.004 40 0.21 0.87 1/0.005 40 0.26 0.89 1/0.007 40 0.33 0.91 1/0.008 40 0.55 0.98 1/0.014 30 0.33 0.71 1/0.011 30 0.55 0.78 1/0.018 30 1 0.93 1/0.033 20 1 0.73 1/0.05 120 2 1.07 1/0.1 23 C. albicans 24 hour 50 ATCC# 10231 2.1 40 0.1 0.85 1/0.0025 40 0.15 0.87 1/0.0038 40 0.21 0.90 1/0.0053 40 0.26 0.92 1/0.0065 40 0.33 0.96 1/0.0083 30 0.15 0.67 1/0.005 30 0.21 0.70 1/0.007 30 0.26 0.72 1/0.0087 80 0.33 0.76 1/0.011 30 0.44 0.81 1/0.015 30 0.55 0.86 1/0.018 20 0.55 0.66 1/0.028 20 1 0.88 1/0.05 10 1.5 0.91 1/0.15 48 hour 50 - 2.6 30 0.55 0.81 1/0.018 30 1 0.98 1/0.033 1 1 ._20 1,0 0.98 1/0.075 24 Ca'= Component A (propiconazole) Cb = Component B (copper 8-hydroxyquinoline) Ratio = Ca/Cb Test Organisms Contact Time Ca Cb S.I. Ca/Cb S. aureus 24 hour 100 3.3 90 0.6 1.08 1/0.007 70 1 1 1/0.014 60 1.5 1.06 1/0.025 50 1.5 0.95 1/0.03 40 2.1 1.04 1/0.053 48 hour 100 3.3 90 0.6 1.08 1/0.007 C. albicans 24 hour 50 ATCC# 10231 19.5 40 0.9 0.85 1/0.023 40 1.3 0.87 1/0.033 40 1.6 0.88 1/0.04 40 2 0.90 110.05 40 2.6 0.93 1/0.065 40 3.3 0.97 1/0.083 30 2.6 0.73 1/0.087 30 3.3 0.77 1/0.11 30 6 0.91 1/0.2 20 9 0.86 1/0.45 20 12.8 1.06 1/0.64 10 9 0.66 1/0.9 10 12.8 0.86 1/1.28 48 hour 60 19.5 40 1.3 0.87 1/0.033 40 1.6 0.88 1/0.04 40 2 0.90 1/0.05 40 2.6 0.93 1/0.065 40 3.3 0.97 1/0.083 30 2.6 0.73 1/0.087 30 3.3 0.77 1/0.11 30 6 0.91 1/0.2 A. niger 3 days 20 ATCC# 16404 6 15 1.3 0.97 1/0.087 10 2 0.83 1/0.2 7days 25 6 15 2 0.93 1/0.93 25 Ca = Component A (propiconazole) Cb = Component B (DCOIT) Ratio = Ca/Cb Test Organisms Contact Time Ca Cb S.I. Ca/Cb S. aureus 24 hour 100 - 0.2 90 0.2 1 1/0.002 90 0.03 1.05 1/0.003 A. niger 3 days 20 - ATCC # 16404 - 2.6 15 0.39 0.90 1/0.026 15 0.53 0.95 1/0.035 10 0.66 0.75 1/0.066 10 1.2 0.96 1/0.12 5 1.8 0.94 1/0.36 7 days 20 - 3.2 10 1.2 0.88 1/0.875 26 Ca = Component A (propiconazole) Cb = Component B (0IT) Ratio = Ca/Cb Test Organisms Contact Time Ca Cb S.I. Ca/Cb Ps. Aeruginosa 24 hour 800 - ATCC# 9027 - 390 500 180 1.09 1/0.36 48 hour 800 ' 526 600 180 1.09 1/0.3 S. aureus 24 hour 100 - 63 90 0.4 0.91 1/0.004 80 0.6 0.81 1/0.008 70 2.4 0.74 1/0.034 60 2.4 0.64 1/0.04 50 13 0.71 1/0.26 50 24 0.88 1/0.48 50 36 1.07 1/0.72 60 24 0.98 1/0.4 -70 10.5 0.87 1/0.25 70 13.2 0.91 1/0.19 70 24 1.08 1/0.34 80 13.2 1.01 1/0.167 90 10.5 1.07 1/0.12 48 hour 100 78 90 0.8 0.91 1/0.009 80 1.1 0.81 1/0.014 70 6.3 0.78 1/0.09 60 7.8 0.7 1/0.13 50 13 0.67 1/0.26 40 51 1.05 1/1.28 50 36 0.96 1/0.72 60 24 0.91 1/0.4 60 36 1.06 1/0.6 70 24 1.01 1/0.34 80 13 0.97 1/0.16 90 13 1.07 1/0.14 1 1_ 90 10.5 1.03 | 1/0.12 27 C. albicans 24 hour 50 ATCC# 10231 1.3 40 0.06 0.85 1/0.0015 30 0.06 0.65 1/0.002 20 0.33 0.65 1/0.0165 10 0.6 0.66 1/0.06 40 0.09 0.87 1/0.0023 40 0.13 0.90 1/0.0033 40 0.16 0.92 1/0.004 40 0.2 0.95 1/0.005 30 0.09 0.67 1/0.003 30 0.13 0.70 1/0.004 30 0.16 0.72 1/0.005 30 0.2 0.75 1/0.007 30 0.26 0.80 1/0.009 30 0.33 0.85 1/0.011 20 0.6 0.86 1/0.03 10 0.9 0.89 1/0.09 48 hour 50 1.3 40 0.09 0,87 1/0.0023 20 0.6 0.86 1/0.03 40 0.13 0.90 1/0.003 40 0.16 0.92 1/0.004 40 0.2 0.95 1/0.005 Ca = Component A (propiconazole) Cb = Component B (CMIT/MIT) Ratio = Ca/Cb Test Organisms Contact Time Ca Cb S.I. Ca/Cb S. aureus 24 hour 100 60 0.44 1.04 1/0.007 50 0.44 0.94 1/0.009 40 0.44 0.84 1/0.011 40 0.55 0.95 1/0.014 50 0.55 1.05 1/0.011 C. albicans 24 hour 50 ATCC # 10231 - 2.6 40 0.44 0.97 1/0.011 30 1 0.98 1/0.033 20 1.5 0.98 1/0.075 A. niger 3 days 20 - ATCC # 16404 2.6 15 0.4 0.90 1/0.027 10 1.2 0.96 1/0.12 28 Ca = Component A (propiconazole) Cb = Component B (IPBC) Ratio = Ca/Cb Test Organisms Contact Time Ca Cb S.I. Ca/Cb A. niger 3 days 20 ATCC # 16404 - 0.4 15 0.01 0.78 1/0.0007 15 0.02 0.80 1/0.0013 15 0.03 0.83 1/0.002 15 0.04 0.85 1/0.0027 15 0.05 0.88 1/0.0033 15 0.07 0.93 1/0.0047 15 0.09 0.98 1/0.006 10 0.11 0.78 1/0.011 Ca = Component A (DCOIT) Cb = Component B (thifluzamide) Ratio = Ca/Cb Test Organisms Contact Time Ca Cb S.I. Ca/Cb G. trabeum 4 weeks 320 ATCC # 11539 - >960 - 80 80 <0.33 1/1 T. vesicolor 4 weeks 320 ATCC # 42462 320 80 80 0.5 1/1 The reference in this specification to any prior publication (or information derived from it), or to any matter which is known, is not, and should not be taken as an acknowledgment or admission or any form of suggestion that that prior publication (or information derived from it) or known matter forms part of the common general knowledge in the field of endeavour to which this specification relates. Throughout this specification and the claims which follow, unless the context requires otherwise, the word "comprise', and variations such as "comprises" and "comprising", will be understood to imply the inclusion of a stated integer or step or group of integers or steps but not the exclusion of any other integer or step or group of integers or steps.