AU2013231142A1 - Synergistic antimicrobial composition - Google Patents
Synergistic antimicrobial composition Download PDFInfo
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- AU2013231142A1 AU2013231142A1 AU2013231142A AU2013231142A AU2013231142A1 AU 2013231142 A1 AU2013231142 A1 AU 2013231142A1 AU 2013231142 A AU2013231142 A AU 2013231142A AU 2013231142 A AU2013231142 A AU 2013231142A AU 2013231142 A1 AU2013231142 A1 AU 2013231142A1
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- naopp
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- tris
- ppm
- phenylphenol
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- 239000000203 mixture Substances 0.000 title claims abstract description 19
- 230000000845 anti-microbial effect Effects 0.000 title claims abstract description 18
- 230000002195 synergetic effect Effects 0.000 title claims abstract description 9
- LLEMOWNGBBNAJR-UHFFFAOYSA-N biphenyl-2-ol Chemical compound OC1=CC=CC=C1C1=CC=CC=C1 LLEMOWNGBBNAJR-UHFFFAOYSA-N 0.000 claims abstract description 31
- 150000003863 ammonium salts Chemical class 0.000 claims abstract description 15
- 235000010292 orthophenyl phenol Nutrition 0.000 claims abstract description 15
- 239000004306 orthophenyl phenol Substances 0.000 claims abstract description 15
- 229910052783 alkali metal Inorganic materials 0.000 claims abstract description 14
- 150000001340 alkali metals Chemical class 0.000 claims abstract description 14
- HUHGPYXAVBJSJV-UHFFFAOYSA-N 2-[3,5-bis(2-hydroxyethyl)-1,3,5-triazinan-1-yl]ethanol Chemical compound OCCN1CN(CCO)CN(CCO)C1 HUHGPYXAVBJSJV-UHFFFAOYSA-N 0.000 claims abstract description 7
- 230000003115 biocidal effect Effects 0.000 description 24
- 239000003139 biocide Substances 0.000 description 18
- OLQJQHSAWMFDJE-UHFFFAOYSA-N 2-(hydroxymethyl)-2-nitropropane-1,3-diol Chemical compound OCC(CO)(CO)[N+]([O-])=O OLQJQHSAWMFDJE-UHFFFAOYSA-N 0.000 description 15
- 150000001875 compounds Chemical class 0.000 description 11
- 244000005700 microbiome Species 0.000 description 9
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 9
- 239000003921 oil Substances 0.000 description 8
- 230000001580 bacterial effect Effects 0.000 description 7
- 239000007789 gas Substances 0.000 description 6
- 239000012530 fluid Substances 0.000 description 5
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 4
- 239000004480 active ingredient Substances 0.000 description 4
- 239000011734 sodium Substances 0.000 description 4
- GUQMDNQYMMRJPY-UHFFFAOYSA-N 4,4-dimethyl-1,3-oxazolidine Chemical compound CC1(C)COCN1 GUQMDNQYMMRJPY-UHFFFAOYSA-N 0.000 description 3
- 241000894006 Bacteria Species 0.000 description 3
- JCXJVPUVTGWSNB-UHFFFAOYSA-N Nitrogen dioxide Chemical class O=[N]=O JCXJVPUVTGWSNB-UHFFFAOYSA-N 0.000 description 3
- 239000007983 Tris buffer Substances 0.000 description 3
- 241001148470 aerobic bacillus Species 0.000 description 3
- -1 bacteristats Substances 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 230000000813 microbial effect Effects 0.000 description 3
- LENZDBCJOHFCAS-UHFFFAOYSA-N tris Chemical compound OCC(N)(CO)CO LENZDBCJOHFCAS-UHFFFAOYSA-N 0.000 description 3
- 241001148471 unidentified anaerobic bacterium Species 0.000 description 3
- ZRALSGWEFCBTJO-UHFFFAOYSA-N Guanidine Chemical compound NC(N)=N ZRALSGWEFCBTJO-UHFFFAOYSA-N 0.000 description 2
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 2
- 230000002401 inhibitory effect Effects 0.000 description 2
- 239000010985 leather Substances 0.000 description 2
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- 239000011780 sodium chloride Substances 0.000 description 2
- 241000195493 Cryptophyta Species 0.000 description 1
- 241000233866 Fungi Species 0.000 description 1
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 1
- CHJJGSNFBQVOTG-UHFFFAOYSA-N N-methyl-guanidine Natural products CNC(N)=N CHJJGSNFBQVOTG-UHFFFAOYSA-N 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 241000589517 Pseudomonas aeruginosa Species 0.000 description 1
- 240000004808 Saccharomyces cerevisiae Species 0.000 description 1
- 241000191967 Staphylococcus aureus Species 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 239000003619 algicide Substances 0.000 description 1
- 230000000844 anti-bacterial effect Effects 0.000 description 1
- 239000004599 antimicrobial Substances 0.000 description 1
- 239000003899 bactericide agent Substances 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 229910052792 caesium Inorganic materials 0.000 description 1
- TVFDJXOCXUVLDH-UHFFFAOYSA-N caesium atom Chemical compound [Cs] TVFDJXOCXUVLDH-UHFFFAOYSA-N 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 239000000498 cooling water Substances 0.000 description 1
- 239000003599 detergent Substances 0.000 description 1
- SWSQBOPZIKWTGO-UHFFFAOYSA-N dimethylaminoamidine Natural products CN(C)C(N)=N SWSQBOPZIKWTGO-UHFFFAOYSA-N 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 239000000446 fuel Substances 0.000 description 1
- 239000000417 fungicide Substances 0.000 description 1
- 239000008235 industrial water Substances 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 239000000976 ink Substances 0.000 description 1
- 239000011499 joint compound Substances 0.000 description 1
- 239000004816 latex Substances 0.000 description 1
- 229920000126 latex Polymers 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- 238000005555 metalworking Methods 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 239000003345 natural gas Substances 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 125000001453 quaternary ammonium group Chemical group 0.000 description 1
- 238000001223 reverse osmosis Methods 0.000 description 1
- 229910052701 rubidium Inorganic materials 0.000 description 1
- IGLNJRXAVVLDKE-UHFFFAOYSA-N rubidium atom Chemical compound [Rb] IGLNJRXAVVLDKE-UHFFFAOYSA-N 0.000 description 1
- 239000012266 salt solution Substances 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
- 238000000108 ultra-filtration Methods 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
- 239000002351 wastewater Substances 0.000 description 1
Landscapes
- Agricultural Chemicals And Associated Chemicals (AREA)
Abstract
A synergistic antimicrobial composition comprising: (a) ortho-phenylphenol or its alkali metal or ammonium salts; and (b) hexahydro-1,3,5-tris(2-hydroxyethyl)-s-triazine; wherein a weight ratio of ortho-phenylphenol or its alkali metal or ammonium salts to hexahydro-1,3,5-tris(2-hydroxyethyl)-s-triazine is from 15:1 to 1:15.
Description
1 SYNERGISTIC ANTIMICROBIAL COMPOSITION The present application is a divisional application from Australian Patent Application Number 2010298539, which claims priority from United States Provisional Application No. 61/277,541, filed 25 September 2009, which is hereby incorporated by reference in its entirety. This invention relates to combinations of biocides, the 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 concentrations, due to weak activity against certain types of microorganisms, or relatively slow antimicrobial action, or instability under certain conditions such as high temperature and high pH. Combinations of different antimicrobial compounds are sometimes used to provide overall control of microorganisms or to provide the same level of microbial control at lower use rates in a particular end use environment. For example, U.S. Pat. No. 7,262,222 discloses combinations of ortho-phenylphenol and a guanidine biocide or a quaternary ammonium biocide, 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 to provide effective control of microorganisms. The problem addressed by this invention is to provide such combinations of antimicrobial compounds. The discussion of documents, acts, materials, devices, articles and the like is included in this specification solely for the purpose of providing a context for the present invention. It is not suggested or represented that any or all of these matters formed part of the prior art base or were common general knowledge in the field relevant to the present invention as it existed before the priority date of each claim of this application. Where the terms "comprise", "comprises", "comprised" or "comprising" are used in this specification (including the claims) they are to be interpreted as specifying the presence of the stated features, integers, steps or components, but not precluding the presence of one or more other features, integers, steps or components, or group thereof. STATEMENT OF THE INVENTION The present invention is directed to a synergistic antimicrobial composition comprising: (a) ortho-phenylphenol or its alkali metal or ammonium salts; and 1 a (b) 4,4-dimethyloxazolidine (DMOZ); wherein a weight ratio of ortho-phenylphenol or its alkali metal or ammonium salts to 4,4-dimethyloxazolidine is from 4:1 to 1.15. The present invention is further directed to a synergistic antimicrobial composition comprising: (a) ortho-phenylphenol or its alkali metal or ammonium salts; and (b) tris(hydroxymethyl)nitromethane (Tris Nitro); wherein a weight ratio of ortho phenylphenol or its alkali metal or ammonium salts to tris(hydroxymethyl)nitromethane is from 15:1 to 1:15. The present invention is further directed to a synergistic antimicrobial composition comprising: (a) ortho-phenylphenol or its alkali metal or ammonium salts; and (b) hexahydro-1,3,5-tris(2-hydroxyethyl)-s-triazine (HHT); wherein a weight ratio of ortho phenylphenol or its alkali metal or ammonium salts to hexahydro-1,3,5-tris(2-hydroxyethyl) s-triazine is from 15:1 to 1:15.
WO 2011/037790 2 PCT/US2010/048845 DETAILED DESCRIPTION OF THE INVENTION As used herein, the following terms have the designated definitions, unless the context clearly indicates otherwise. The term "antimicrobial compound" refers to a compound capable of inhibiting the growth or propagation of microorganisms, and/or killing 5 microorganisms; antimicrobial compounds include bactericides, bacteristats, fungicides, fungistats, algaecides and algistats, depending on the dose level applied, system conditions and the level of microbial control desired. The term "microorganism" includes, for example, fungi (such as yeast and mold), bacteria and algae. The following abbreviations are used throughout the specification: ppm= parts per million by weight (weight/weight), mL = 0 milliliter, Unless otherwise specified, temperatures are in degrees centigrade ('C), and references to percentages are by weight (wt%). Percentages of antimicrobial compounds in the 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. Ortho 5 phenylphenol or its alkali metal or ammonium salts includes lithium, sodium, potassium, rubidium, cesium and ammonium salts. If more than one form of ortho-phenylphenol is present, the biocide ratio is calculated from the total content of such compounds. In some embodiments of the invention, sodium o-phenylphenylate (NaOPP) is used. In some embodiments of the invention, a weight ratio of the ortho-phenylphenol or its alkali metal or ammonium salts to 4,4-dimethyloxazolidine (DMOZ) is from 3:1 to 1:12, alternatively from 3:1 to 1:10, alternatively from 3:1 to 1:9, alternatively from 2:1 to 1:15, alternatively from 2:1 to 1:10, alternatively from 1:1 to 1:12, alternatively from 1:1 to 1:10, alternatively from 1:1 to 1:9. In some embodiments of the invention, a weight ratio of the ortho-phenylphenol or its alkali metal or ammonium salts to tris(hydroxymethyl)nitromethane (Tris Nitro) is from 15:1 to 1:12, alternatively from 15:1 to 1:10, alternatively from 12:1 to 1:12, alternatively from 12:1 to 1:10, alternatively from 10:1 to 1:10, alternatively from 10:1 to 1:9, alternatively from 9:1 to 1:9. In some embodiments of the invention, a weight ratio of the ortho-phenylphenol or its alkali metal or ammonium salts to hexahydro-1,3,5-tris(2-hydroxyethyl)-s-triazine is from 12:1 to 1:15, alternatively from 10:1 to 1:15, alternatively from 10:1 to 1:12, alternatively from 10:1 to 1:10, alternatively from 9:1 to 1:10, alternatively from 9:1 to 1:9.
WO 2011/037790 3 PCT/US2010/048845 In some embodiments of the invention, the antimicrobial combination of this invention is useful in oil and gas field injection, produced fluids, fracturing fluids and other functional fluids, oil and gas wells, oil and gas operation, separation, storage, and transportation systems, oil and gas pipelines, oil and gas vessels, and fuel. The combination 5 is especially useful in aqueous fluids added to or produced by oil and gas well. The composition also is useful for controlling microorganisms in other industrial water and water containing/contaminated matrixes, such as cooling water, air washer, heat exchangers, boiler water, pulp and paper mill water, other industrial process water, ballast water, wastewater, metalworking fluids, latex, paint, coatings, adhesives, inks, tape joint compounds, pigment, 0 water-based slurries, personal care and household products such as detergent, filtration systems (including reverse osmosis and ultrafiltration systems), toilet bowel, textiles, leather and leather production system, or a system used therewith. Typically, the amount of the biocide combinations of the present invention to control the growth of microorganisms is from 10 ppm to 5,000 ppm active ingredient. In some 5 embodiments of the invention, the active ingredients of the composition are present in an amount of at least 20 ppm, alternatively at least 50 ppm, alternatively at least 100 ppm, alternatively at least 150 ppm, alternatively at least 200 ppm. In some embodiments, the active ingredients of the composition are present in an amount of no more than 2,000 ppm, alternatively no more than 1,000 ppm, alternatively no more than 500 ppm, alternatively no 0 more than 400 ppm, alternatively no more than 300 ppm, alternatively no more than 250 ppm, alternatively no more than 200 ppm, alternatively no more than 100 ppm, alternatively no more than 50 ppm. Concentrations mentioned above are in a liquid composition containing the biocide combinations. Biocide concentrations in a high-sulfide and high temperature environment typically will be higher than in other environments. 25 The present invention also encompasses a method for reducing, or inhibiting, or preventing microbial growth in the use areas described above, especially in oil or natural gas production operations, by incorporating the claimed biocide combination into the materials.
WO 2011/037790 4 PCT/US2010/048845 EXAMPLES Example 1. Synergistic effect of NaOPP and DMOZ or Tris Nitro or HHT against sulfate reducing bacteria (SRB) 5 Inside an anaerobic chamber (BACTRON anaerobic chamber), a deaerated sterile salt solution (3.1183 g of NaCl, 1.3082 mg of NaHCO 3 , 47.70 mg of KCl, 72.00 mg of CaCl 2 , 54.49 mg of MgSO 4 , 172.28 mg of Na 2
SO
4 , 43.92 mg of Na 2
CO
3 in 1 L water) was contaminated with an oil field isolated anaerobic consortium, mainly SRB, at final bacterial concentrations of 101 to107 CFU/mL. The aliquots of this contaminated water were then 0 treated with NaOPP and DMOZ, or the NaOPP/DMOZ combination, NaOPP and Tris Nitro, or the NaOPP/Tris Nitro combination, NaOPP and HHT, or the NaOPP/HHT combination at different active concentration levels. After the mixtures were incubated at 40'C for 24 hours, the biocidal efficacy was determined by minimum tested biocide concentration for complete bacterial kill in the aliquots (MBC). Tables 1-3 summarize the efficacy of each biocide and 5 their blends, and the Synergy Index of each combination. Table 1. Biocidal efficacy of NaOPP, DMOZ and NaOPP/DMOZ combination against anaerobic bacteria, and Synergy Index MBC (active Ratio of NaOPP to ppm) Synergy DMOZ (active w/w) NaOPP DMOZ Index* 1:0 333.3 0.0 9:1 181.8 20.2 0.82 3:1 133.3 44.4 1.00 1:1 49.4 49.4 0.81 1:3 14.1 42.3 0.61 1:9 5.2 46.8 0.65 0:1 0.0 74.1 20 * Synergy Index= Ca /CA + Cb/CB Ca: Concentration of biocide A required to achieve complete bacterial kill when used in combination with biocide B CA: Concentration of biocide A required to achieve complete bacterial kill when used alone Cb: Concentration of biocide B required to achieve complete bacterial kill when used in 25 combination with biocide A CB: Concentration of biocide B required to achieve complete bacterial kill when used alone WO 2011/037790 5 PCT/US2010/048845 Table 2. Biocidal efficacy of NaOPP, Tris Nitro and NaOPP/Tris Nitro combination against anaerobic bacteria, and Synergy Index MBC (active Ratio of NaOPP to Tris ppm) Synergy Nitro (active w/w) NaOPP Tris Index Nitro 1:0 500 0.0 9:1 108.1 12.0 0.49 3:1 70.2 23.4 0.67 1:1 22.8 22.8 0.56 1:3 9.0 26.9 0.62 1:9 3.2 28.7 0.65 0:1 0.0 44.4 5 Table 3. Biocidal efficacy of NaOPP, HHT and NaOPP/HHT combination against anaerobic bacteria, and Synergy Index MBC (active Ratio of NaOPP to ppm) Synergy HHT (active w/w) NaOPP HHT Index 1:0 500 0.0 9:1 272.7 30.3 0.82 3:1 133.3 44.4 0.67 1:1 49.4 49.4 0.54 1:3 21.2 63.5 0.61 1:9 7.8 70.2 0.65 0:1 0.0 111.1 10 Example 2. Synergistic effect of NaOPP and DMOZ or Tris Nitro against aerobic bacteria A sterile NaCl solution (0.85%) was contaminated with Pseudomonas aeruginosa, ATCC 10145 and Staphylococcus aureus, ATCC 6538 at final bacterial concentration of ca. 106 CFU/mL. The aliquots of this contaminated water were then treated with NaOPP and Tris 15 Nitro, or the NaOPP/Tris Nitro combination, NaOPP and DMOZ or the NaOPP/DMOZ combination at different active concentration levels. After the mixtures were incubated at 37'C for 24 hours, the biocidal efficacy was determined by minimum tested biocide concentration for complete bacteria kill in the aliquots. Tables 4 and 5 summarize the efficacy of each biocide and their blends, and the Synergy Index of each combination.
WO 2011/037790 6 PCT/US2010/048845 Table 4. Biocidal efficacy of NaOPP, DMOZ and NaOPP/DMOZ combination against aerobic bacteria, and Synergy Index Average MBC Average Ratio of NaOPP to (active ppm) Synergy p value DMOZ (active w/w) NaOPP DMOZ Inder in ztest* 1:0 292.9 0.0 8.12:1 209.6 25.7 1.03 0.53 2.86:1 111.9 38.8 0.85 0.00 1:1 50.9 50.9 0.78 0.00 1:2.86 19.3 55.2 0.72 0.00 1:8.12 6.8 55.2 0.67 0.00 0:1 0.0 86.1 5 * P value < 0.05 means that there is significant difference between the average Synergy Index and 1.00 Table 5. Biocidal efficacy of NaOPP, Tris Nitro, and NaOPP/Tris Nitro combination against aerobic bacteria, and Synergy Index Ratio of NaOPP to MBC (active Tris Nitro (active T. Synergy w/w) NaOPP NTris Index 1:0 266.3 0.0 8.12:1 93.2 11.4 0.81 2.86:1 55.2 19.1 0.97 1:1 <14.9 <14.9 <0.65 1:2.86 <6.8 <19.3 <0.79 1:8.12 <2.4 <19.3 <0.78 0:1 0.0 25.1 [0
Claims (3)
1. A synergistic antimicrobial composition comprising: (a) ortho-phenylphenol or its alkali metal or ammonium salts; and (b) hexahydro-1,3,5-tris(2-hydroxyethyl)-s-triazine; wherein a weight ratio of ortho-phenylphenol or its alkali metal or ammonium salts to hexahydro-1,3,5-tris(2-hydroxyethyl)-s-triazine is from 15:1 to 1:15.
2. The composition of claim 1 in which the weight ratio is from 10:1 to 1:12.
3. The composition of claim 2 in which the weight ratio is from 9:1 to 1:10.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| AU2013231142A AU2013231142A1 (en) | 2009-09-25 | 2013-09-23 | Synergistic antimicrobial composition |
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US61/277,541 | 2009-09-25 | ||
| AU2010298539A AU2010298539B2 (en) | 2009-09-25 | 2010-09-15 | Synergistic antimicrobial composition |
| AU2013231142A AU2013231142A1 (en) | 2009-09-25 | 2013-09-23 | Synergistic antimicrobial composition |
Related Parent Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AU2010298539A Division AU2010298539B2 (en) | 2009-09-25 | 2010-09-15 | Synergistic antimicrobial composition |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AU2013231142A1 true AU2013231142A1 (en) | 2013-10-10 |
Family
ID=49302359
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AU2013231142A Abandoned AU2013231142A1 (en) | 2009-09-25 | 2013-09-23 | Synergistic antimicrobial composition |
| AU2013231143A Ceased AU2013231143B2 (en) | 2009-09-25 | 2013-09-23 | Synergistic antimicrobial composition |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AU2013231143A Ceased AU2013231143B2 (en) | 2009-09-25 | 2013-09-23 | Synergistic antimicrobial composition |
Country Status (1)
| Country | Link |
|---|---|
| AU (2) | AU2013231142A1 (en) |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1287259B (en) * | 1967-04-26 | 1969-01-16 | Henkel & Cie Gmbh | Use of nitro alcohols as potentizing agents in antimicrobial agents |
-
2013
- 2013-09-23 AU AU2013231142A patent/AU2013231142A1/en not_active Abandoned
- 2013-09-23 AU AU2013231143A patent/AU2013231143B2/en not_active Ceased
Also Published As
| Publication number | Publication date |
|---|---|
| AU2013231143A1 (en) | 2013-10-10 |
| AU2013231143B2 (en) | 2016-05-19 |
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| MK5 | Application lapsed section 142(2)(e) - patent request and compl. specification not accepted |