WO2011038320A2 - Compositions of dibromomalonamide and their use as biocides - Google Patents
Compositions of dibromomalonamide and their use as biocides Download PDFInfo
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- WO2011038320A2 WO2011038320A2 PCT/US2010/050348 US2010050348W WO2011038320A2 WO 2011038320 A2 WO2011038320 A2 WO 2011038320A2 US 2010050348 W US2010050348 W US 2010050348W WO 2011038320 A2 WO2011038320 A2 WO 2011038320A2
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- water
- dibromomalonamide
- aqueous
- phenylphenol
- fluid
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- SWHQVMGRXIYDSF-UHFFFAOYSA-N NC(C(C(N)=O)(Br)Br)=O Chemical compound NC(C(C(N)=O)(Br)Br)=O SWHQVMGRXIYDSF-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/18—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing the group —CO—N<, e.g. carboxylic acid amides or imides; Thio analogues thereof
- A01N37/30—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing the group —CO—N<, e.g. carboxylic acid amides or imides; Thio analogues thereof containing the groups —CO—N< and, both being directly attached by their carbon atoms to the same carbon skeleton, e.g. H2N—NH—CO—C6H4—COOCH3; Thio-analogues thereof
Definitions
- the invention relates to biocidal compositions and methods of their use for the control of microorganisms in aqueous and water-containing systems.
- the compositions comprise 2,2-dibromomalonamide and a phenolic -based biocidal compound.
- Water systems provide fertile breeding grounds for algae, bacteria, viruses, and fungi some of which can be pathogenic. Microbial contamination can create a variety of problems, including aesthetic unpleasantries such as slimy green water, serious health risks such as fungal, bacterial, or viral infections, and mechanical problems including plugging, corrosion of equipment, and reduction of heat transfer.
- Biocides are commonly used to disinfect and control the growth of microorganisms in aqueous and water containing systems. However, not all biocides are effective against a wide range of microorganisms and/or temperatures, and some are incompatible with other chemical treatment additives. In addition, some biocides do not provide microbial control over long enough time periods.
- biocide compositions for treatment of water systems that yield one or more of the following advantages: increased efficacy at lower concentrations, compatibility with physical conditions and other additives in the treated medium, effectiveness against a broad spectrum of microorganisms, and/or ability to provide both short term and long term control of microorganisms.
- the invention provides a biocidal composition.
- the composition is useful for controlling microorganisms in aqueous or water containing systems.
- the composition comprises: 2,2-dibromomalonamide and sodium ortho-phenylphenol (SOPP).
- the invention provides a method for controlling microorganisms in aqueous or water containing systems.
- the method comprises treating the system with an effective amount of a biocidal composition as described herein.
- the invention provides a biocidal composition and methods of using it in the control of microorganisms.
- the composition comprises: 2,2-dibromomalonamide and sodium ortho-phenylphenol (SOPP). It has surprisingly been discovered that combinations of 2,2-dibromomalonamide and sodium ortho-phenylphenol as described herein, at certain weight ratios, are synergistic when used for microorganism control in aqueous or water containing media. That is, the combined materials result in improved biocidal properties than would otherwise be expected based on their individual performance. The synergy permits reduced amounts of the materials to be used to achieve the desired biocidal performance, thus reducing problems caused by growth of microorganisms in industrial process waters while potentially reducing environmental impact and materials cost.
- SOPP sodium ortho-phenylphenol
- microorganism includes, but is not limited to, bacteria, fungi, algae, and viruses.
- control and controlling should be broadly construed to include within their meaning, and without being limited thereto, inhibiting the growth or propagation of microorganisms, killing microorganisms, disinfection, and/or preservation. In some preferred embodiments, "control” and
- controlling mean inhibiting the growth or propagation of microorganisms.
- 2,2-dibromomalonamide refers to a compound represented by the following chemical formula:
- 2,2-Dibromomalonamide and the sodium ortho-phenylphenol of the invention are commercially available and/or can be readily prepared by those skilled in the art using well known techniques.
- the weight ratio of 2,2-dibromomalonamide to sodium ortho-phenylphenol is between about 100:1 and about 1:100.
- the weight ratio of 2,2-dibromomalonamide to sodium ortho- phenylphenol is between about 50:1 and about 1:50.
- the weight ratio of 2,2-dibromomalonamide to sodium ortho- phenylphenol is between about 10:1 and about 1:30. In some embodiments, the weight ratio of 2,2-dibromomalonamide to the sodium ortho-phenylphenol is between about 1: 1 and about 1:20.
- the weight ratio of 2,2-dibromomalonamide to sodium ortho- phenylphenol is from about 1:1.25 to about 1:20.
- composition of the invention is useful for controlling microorganisms in a variety of aqueous and water containing systems.
- aqueous and water containing systems include, but are not limited to, paints and coatings, aqueous emulsions, latexes, adhesives, inks, pigment dispersions, household and industrial cleaners, detergents, dish detergents, mineral slurries polymer emulsions, caulks and adhesives, tape joint compounds, disinfectants, sanitizers, metalworking fluids, construction products, personal care products, textile fluids such as spin finishes, industrial process water (e.g.
- oilfield water, pulp and paper water, cooling water oilfield functional fluids such as drilling muds and fracturing fluids, fuels, air washers, wastewater, ballast water, filtration systems, and swimming pool and spa water.
- oilfield functional fluids such as drilling muds and fracturing fluids, fuels, air washers, wastewater, ballast water, filtration systems, and swimming pool and spa water.
- Preferred aqueous systems are metal working fluids, personal care, household and industrial cleaners, industrial process water, and paints and coatings. Particularly preferred are industrial process water, paints and coatings, metal working fluids, and textile fluids such as spin finishes.
- a suitable actives concentration (total for both 2,2-dibromomalonamide and sodium ortho- phenylphenol) is typically at least about 1 ppm, alternatively at least about 3 ppm, alternatively at least about 7 ppm, alternatively at least about 10 ppm, or alternatively at least about 100 ppm based on the total weight of the aqueous or water containing system.
- a suitable upper limit for the actives concentration is about 1000 ppm, alternatively about 500 ppm, alternatively about 100 ppm, alternatively about 50 ppm, alternatively about 30 ppm, alternatively about 15 ppm, alternatively about 10 ppm, or alternatively about 7 ppm, based on the total weight of the aqueous or water containing system.
- the actives concentration is between about 10 and about 135 ppm.
- compositions can be added to the aqueous or water containing system separately, or pre-blended prior to addition.
- a person of ordinary skill in the art can easily determine the appropriate method of addition.
- the composition can be used in the system with other additives such as, but not limited to, surfactants, ionic/nonionic polymers and scale and corrosion inhibitors, oxygen scavengers, and/or additional biocides.
- the growth inhibition assay used in the Examples measures inhibition of growth (or lack thereof) of a microbial consortium. Inhibition of growth can be the result of killing of the cells (so no growth occurs), killing of a significant portion of the populations of cells so that regrowth requires a prolonged time, or inhibition of growth without killing (stasis). Regardless of the mechanism of action, the impact of a biocide (or combination of biocides) can be measured over time on the basis of an increase in the size of the community.
- the assay measures the efficacy of one or more biocides at preventing growth of a consortium of bacteria in a dilute mineral salts medium.
- the medium contains (in mg/1) the following components: FeCl 3 .6H 2 0 (1); CaCl 2 .2H 2 0 (10); MgS0 4 .7H 2 0 (22.5); (NH 4 ) 2 S0 4 (40); KH 2 P0 4 (10); K 2 HP0 4 (25.5); Yeast Extract (10); and glucose (100). After all components are added to deionized water, the pH of the medium is adjusted to 7.5. Following filter sterilization, aliquots are dispensed in 100 ul quantities to sterile microtiter plate wells.
- Dilutions of 2,2-dibromomalonamide (“DBMAL”) and/or "Biocide B” are then added to the microtiter plate.
- each well is inoculated with 100 ⁇ of a cell suspension containing ca. 1 x 10 6 cells per milliliter of a mixture of Pseudomonas aeruginosa, Klebsiella pneumoniae, Staphylococcus aureus, and Bacillus subtilis.
- the final total volume of medium in each well is 300 ⁇ .
- the concentration of each active ranges from 25 ppm to 0.195 ppm as illustrated in Table 1.
- the resulting matrix allows testing of eight concentrations of each active and 64 combinations of actives in the ratios (of actives).
- Controls (not shown) contain the medium with no biocide added.
- each well is inoculated with 100 ⁇ of a cell suspension containing ca. 1 x 10 6 cells per milliliter of a mixture of Pseudomonas aeruginosa, Klebsiella pneumoniae, Staphylococcus aureus, and Bacillus subtilis.
- the final total volume of medium in each well is 300 ⁇ .
- the optical density (OD) readings for each well is measured at 580 nm and the plates are then incubated at 37 °C for 24 nr. After the incubation period, the plates are gently agitated before OD5 80 values are collected. The OD5 80 values at T 0 are subtracted from T 24 values to determine the total amount of growth (or lack thereof) that occurs. These values are used to calculate the percent inhibition of growth caused by the presence of each biocide and each of the 64 combinations. A 90% inhibition of growth is used as a threshold for calculating synergy index (SI) values with the following equation:
- Table 2 shows the assay results for DBMAL, sodium ortho-phenylphenol ("SOPP"), and combinations.
- concentrations of DBMAL and SOPP needed to prevent at least 90% of the growth (3 ⁇ 4o) of the microbial consortium are 12.5 mg/1 and 500 mg/1, respectively (Table 2).
- Combinations of the actives (in which each was less than its 3 ⁇ 4o value) that cause at least 90% inhibition ranged from 3.13 mg/1 DBMAL plus 250 mg/1 SOPP to 0.39 mg/1 DBMAL plus 250 mg/1 SOPP. As illustrated in Table 3, these represent ratios from 1:1.25 to 1:20 (DBMAL to SOPP).
- Table 3 shows ratios of DBMAL and SOPP found to be synergistic under the growth inhibition assay.
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- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
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Abstract
A biocidal composition comprising 2,2-dibromomalonamide and sodium ortho-phenylphenol, and its use for the control of microorganisms in aqueous and water-containing systems.
Description
COMPOSITIONS OF DIBROMOMALONAMIDE
AND THEIR USE AS BIOCIDES
Cross-reference to Related Applications
This application claims the benefit of U.S. Provisional Application Ser. No.
61/246,190, filed September 28, 2009, which is incorporated herein by reference in its entirety.
Field of the Invention
The invention relates to biocidal compositions and methods of their use for the control of microorganisms in aqueous and water-containing systems. The compositions comprise 2,2-dibromomalonamide and a phenolic -based biocidal compound.
Background of the Invention
Water systems provide fertile breeding grounds for algae, bacteria, viruses, and fungi some of which can be pathogenic. Microbial contamination can create a variety of problems, including aesthetic unpleasantries such as slimy green water, serious health risks such as fungal, bacterial, or viral infections, and mechanical problems including plugging, corrosion of equipment, and reduction of heat transfer.
Biocides are commonly used to disinfect and control the growth of microorganisms in aqueous and water containing systems. However, not all biocides are effective against a wide range of microorganisms and/or temperatures, and some are incompatible with other chemical treatment additives. In addition, some biocides do not provide microbial control over long enough time periods.
While some of these shortcomings can be overcome through use of larger amounts of the biocide, this option creates its own problems, including increased cost, increased waste, and increased likelihood that the biocide will interfere with the desirable properties
of the treated medium. In addition, even with use of larger amounts of the biocide, many commercial biocidal compounds cannot provide effective control due to weak activity against certain types of microorganisms or resistance of the microorganisms to those compounds.
It would be a significant advance in the art to provide biocide compositions for treatment of water systems that yield one or more of the following advantages: increased efficacy at lower concentrations, compatibility with physical conditions and other additives in the treated medium, effectiveness against a broad spectrum of microorganisms, and/or ability to provide both short term and long term control of microorganisms.
BRIEF SUMMARY OF THE INVENTION
In one aspect, the invention provides a biocidal composition. The composition is useful for controlling microorganisms in aqueous or water containing systems. The composition comprises: 2,2-dibromomalonamide and sodium ortho-phenylphenol (SOPP).
In a second aspect, the invention provides a method for controlling microorganisms in aqueous or water containing systems. The method comprises treating the system with an effective amount of a biocidal composition as described herein.
DETAILED DESCRIPTION OF THE INVENTION
As noted above, the invention provides a biocidal composition and methods of using it in the control of microorganisms. The composition comprises: 2,2-dibromomalonamide and sodium ortho-phenylphenol (SOPP). It has surprisingly been discovered that combinations of 2,2-dibromomalonamide and sodium ortho-phenylphenol as described herein, at certain weight ratios, are synergistic when used for microorganism control in aqueous or water containing media. That is, the combined materials result in improved
biocidal properties than would otherwise be expected based on their individual performance. The synergy permits reduced amounts of the materials to be used to achieve the desired biocidal performance, thus reducing problems caused by growth of microorganisms in industrial process waters while potentially reducing environmental impact and materials cost.
For the purposes of this specification, the meaning of "microorganism" includes, but is not limited to, bacteria, fungi, algae, and viruses. The words "control" and "controlling" should be broadly construed to include within their meaning, and without being limited thereto, inhibiting the growth or propagation of microorganisms, killing microorganisms, disinfection, and/or preservation. In some preferred embodiments, "control" and
"controlling" mean inhibiting the growth or propagation of microorganisms.
The term "2,2-dibromomalonamide" refers to a compound represented by the following chemical formula:
2,2-Dibromomalonamide and the sodium ortho-phenylphenol of the invention are commercially available and/or can be readily prepared by those skilled in the art using well known techniques.
In some embodiments of the invention, the weight ratio of 2,2-dibromomalonamide to sodium ortho-phenylphenol is between about 100:1 and about 1:100.
In some embodiments, the weight ratio of 2,2-dibromomalonamide to sodium ortho- phenylphenol is between about 50:1 and about 1:50.
In some embodiments, the weight ratio of 2,2-dibromomalonamide to sodium ortho- phenylphenol is between about 10:1 and about 1:30.
In some embodiments, the weight ratio of 2,2-dibromomalonamide to the sodium ortho-phenylphenol is between about 1: 1 and about 1:20.
In some embodiments, the weight ratio of 2,2-dibromomalonamide to sodium ortho- phenylphenol is from about 1:1.25 to about 1:20.
The composition of the invention is useful for controlling microorganisms in a variety of aqueous and water containing systems. Examples of such systems include, but are not limited to, paints and coatings, aqueous emulsions, latexes, adhesives, inks, pigment dispersions, household and industrial cleaners, detergents, dish detergents, mineral slurries polymer emulsions, caulks and adhesives, tape joint compounds, disinfectants, sanitizers, metalworking fluids, construction products, personal care products, textile fluids such as spin finishes, industrial process water (e.g. oilfield water, pulp and paper water, cooling water), oilfield functional fluids such as drilling muds and fracturing fluids, fuels, air washers, wastewater, ballast water, filtration systems, and swimming pool and spa water. Preferred aqueous systems are metal working fluids, personal care, household and industrial cleaners, industrial process water, and paints and coatings. Particularly preferred are industrial process water, paints and coatings, metal working fluids, and textile fluids such as spin finishes.
A person of ordinary skill in the art can readily determine, without undue experimentation, the effective amount of the composition that should be used in any particular application to provide microorganism control. By way of illustration, a suitable actives concentration (total for both 2,2-dibromomalonamide and sodium ortho- phenylphenol) is typically at least about 1 ppm, alternatively at least about 3 ppm, alternatively at least about 7 ppm, alternatively at least about 10 ppm, or alternatively at least about 100 ppm based on the total weight of the aqueous or water containing system. In
some embodiments, a suitable upper limit for the actives concentration is about 1000 ppm, alternatively about 500 ppm, alternatively about 100 ppm, alternatively about 50 ppm, alternatively about 30 ppm, alternatively about 15 ppm, alternatively about 10 ppm, or alternatively about 7 ppm, based on the total weight of the aqueous or water containing system.
Because of the composition's synergy, lower amounts of the biocides may optionally be used while still advantageously providing control of microorganisms. Thus, in some embodiments, the actives concentration is between about 10 and about 135 ppm.
The components of the composition can be added to the aqueous or water containing system separately, or pre-blended prior to addition. A person of ordinary skill in the art can easily determine the appropriate method of addition. The composition can be used in the system with other additives such as, but not limited to, surfactants, ionic/nonionic polymers and scale and corrosion inhibitors, oxygen scavengers, and/or additional biocides.
The following examples are illustrative of the invention but are not intended to limit its scope. Unless otherwise indicated, the ratios, percentages, parts, and the like used herein are by weight.
EXAMPLES
The results provided in the Examples are generated using a growth inhibition assay. Details of each assay are provided below.
Growth Inhibition Assay. The growth inhibition assay used in the Examples measures inhibition of growth (or lack thereof) of a microbial consortium. Inhibition of growth can be the result of killing of the cells (so no growth occurs), killing of a significant portion of the populations of cells so that regrowth requires a prolonged time, or inhibition of growth without killing (stasis). Regardless of the mechanism of action, the impact of a
biocide (or combination of biocides) can be measured over time on the basis of an increase in the size of the community.
The assay measures the efficacy of one or more biocides at preventing growth of a consortium of bacteria in a dilute mineral salts medium. The medium contains (in mg/1) the following components: FeCl3.6H20 (1); CaCl2.2H20 (10); MgS04.7H20 (22.5); (NH4)2S04 (40); KH2P04 (10); K2HP04 (25.5); Yeast Extract (10); and glucose (100). After all components are added to deionized water, the pH of the medium is adjusted to 7.5. Following filter sterilization, aliquots are dispensed in 100 ul quantities to sterile microtiter plate wells. Dilutions of 2,2-dibromomalonamide ("DBMAL") and/or "Biocide B" are then added to the microtiter plate. After preparing the combinations of actives as illustrated below, each well is inoculated with 100 μΐ of a cell suspension containing ca. 1 x 106 cells per milliliter of a mixture of Pseudomonas aeruginosa, Klebsiella pneumoniae, Staphylococcus aureus, and Bacillus subtilis. The final total volume of medium in each well is 300 μΐ. Once prepared as described herein, the concentration of each active ranges from 25 ppm to 0.195 ppm as illustrated in Table 1. The resulting matrix allows testing of eight concentrations of each active and 64 combinations of actives in the ratios (of actives).
Table 1. Template for microtiter plate-based synergy assay showing concentrations of each active. Ratios are based on weight (ppm) of each active.
Controls (not shown) contain the medium with no biocide added. After preparing the combinations of actives as illustrated above, each well is inoculated with 100 μΐ of a cell
suspension containing ca. 1 x 106 cells per milliliter of a mixture of Pseudomonas aeruginosa, Klebsiella pneumoniae, Staphylococcus aureus, and Bacillus subtilis. The final total volume of medium in each well is 300 μΐ.
Immediately after the microtiter plates are prepared, the optical density (OD) readings for each well is measured at 580 nm and the plates are then incubated at 37 °C for 24 nr. After the incubation period, the plates are gently agitated before OD580 values are collected. The OD580 values at T0 are subtracted from T24 values to determine the total amount of growth (or lack thereof) that occurs. These values are used to calculate the percent inhibition of growth caused by the presence of each biocide and each of the 64 combinations. A 90% inhibition of growth is used as a threshold for calculating synergy index (SI) values with the following equation:
The SI values are interpreted as follows:
SI <1 : Synergistic combination
SI = 1 : Additive combination
SI >1 : Antagonistic combination
In the Examples below, the amounts of biocides in the solution are measured in mg per liter of solution (mg/1). Since solution densities are approximately 1.00, the mg/1 measurement corresponds to weight ppm. Both units may therefore be used interchangeably in the Examples.
Example 1
DBMAL and SOPP
Table 2 shows the assay results for DBMAL, sodium ortho-phenylphenol ("SOPP"), and combinations. The concentrations of DBMAL and SOPP needed to prevent at least 90% of the growth (¾o) of the microbial consortium are 12.5 mg/1 and 500 mg/1, respectively (Table 2). Combinations of the actives (in which each was less than its ¾o value) that cause at least 90% inhibition ranged from 3.13 mg/1 DBMAL plus 250 mg/1 SOPP to 0.39 mg/1 DBMAL plus 250 mg/1 SOPP. As illustrated in Table 3, these represent ratios from 1:1.25 to 1:20 (DBMAL to SOPP).
Table 2. Percent inhibition of growth in a species-defined microbial consortium by DBMAL and SOPP alone and combinations of these actives after a 24-hour incubation period. Numbers represent percent inhibition of growth as measured by optical density measurements (580 nm) at time 24 hours compared with time = 0 values.
Table 3 shows ratios of DBMAL and SOPP found to be synergistic under the growth inhibition assay.
While the invention has been described above according to its preferred
embodiments, it can be modified within the spirit and scope of this disclosure. This application is therefore intended to cover any variations, uses, or adaptations of the invention using the general principles disclosed herein. Further, the application is intended to cover such departures from the present disclosure as come within the known or customary practice in the art to which this invention pertains and which fall within the limits of the following claims.
Claims
1. A biocidal composition comprising: 2,2-dibromomalonamide and sodium ortho- phenylphenol.
2. A composition according to claim 1 wherein the weight ratio of 2,2- dibromomalonamide to sodium ortho-phenylphenol is between about 100:1 and about 1:100.
3. A composition according to claim 1 wherein the weight ratio of 2,2- dibromomalonamide to sodium ortho-phenylphenol is from about 1:1 to about 1:20.
4. A composition according to any one of claims 1-3 which is: paint, coating, aqueous emulsion, latex, adhesive, ink, pigment dispersion, household or industrial cleaner, detergent, dish detergent, mineral slurry polymer emulsion, caulk, adhesive, tape joint compound, disinfectant, sanitizer, metalworking fluid, construction product, personal care product, textile fluid, spin finish, industrial process water, oilfield functional fluid, fuel, air washer, wastewater, ballast water, filtration systems, or swimming pool and spa water.
5. A method for controlling microorganism growth in an aqueous or water-containing system, the method comprising treating the aqueous or water-containing system with an effective amount of a composition according to any one of claims 1-3.
6. A method according to claim 5 wherein the aqueous or water-containing system is paint, coating, aqueous emulsion, latex, adhesive, ink, pigment dispersion, household or industrial cleaner, detergent, dish detergent, mineral slurry polymer emulsion, caulk, adhesive, tape joint compound, disinfectant, sanitizer, metalworking fluid, construction product, personal care product, textile fluid, spin finish, industrial process water, oilfield functional fluid, fuel, air washer, wastewater, ballast water, filtration system, or swimming pool and spa water.
Priority Applications (8)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| MX2012003734A MX2012003734A (en) | 2009-09-28 | 2010-09-27 | Compositions of dibromomalonamide and their use as biocides. |
| EP10760882.0A EP2482652B1 (en) | 2009-09-28 | 2010-09-27 | Compositions of dibromomalonamide and their use as biocides |
| PL10760882T PL2482652T3 (en) | 2009-09-28 | 2010-09-27 | Compositions of dibromomalonamide and their use as biocides |
| CN201080042554.8A CN102548401B (en) | 2009-09-28 | 2010-09-27 | Dibromomalonamide compositions and their use as biocides |
| US13/388,469 US8598234B2 (en) | 2009-09-28 | 2010-09-27 | Compositions of dibromomalonamide and their use as biocides |
| BR112012004923A BR112012004923A2 (en) | 2009-09-28 | 2010-09-27 | biocidal composition to control the growth of microorganisms in an aqueous or water-containing system |
| JP2012531094A JP5744882B2 (en) | 2009-09-28 | 2010-09-27 | Composition of dibromomalonamide and its use as a biocide |
| RU2012117605/13A RU2536923C2 (en) | 2009-09-28 | 2010-09-27 | Dibromomalonamide composition and use thereof as biocide |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US24619009P | 2009-09-28 | 2009-09-28 | |
| US61/246,190 | 2009-09-28 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| WO2011038320A2 true WO2011038320A2 (en) | 2011-03-31 |
| WO2011038320A3 WO2011038320A3 (en) | 2011-09-22 |
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| PCT/US2010/050348 Ceased WO2011038320A2 (en) | 2009-09-28 | 2010-09-27 | Compositions of dibromomalonamide and their use as biocides |
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| Country | Link |
|---|---|
| US (1) | US8598234B2 (en) |
| EP (1) | EP2482652B1 (en) |
| JP (1) | JP5744882B2 (en) |
| CN (1) | CN102548401B (en) |
| BR (1) | BR112012004923A2 (en) |
| MX (1) | MX2012003734A (en) |
| PL (1) | PL2482652T3 (en) |
| RU (1) | RU2536923C2 (en) |
| WO (1) | WO2011038320A2 (en) |
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| WO2012021340A1 (en) * | 2010-08-09 | 2012-02-16 | Dow Global Technologies Llc | Compositions of dibromomalonamide and their use as biocides |
| CN108174868A (en) * | 2017-12-31 | 2018-06-19 | 仙桃市中楚化工有限责任公司 | A kind of strong fungicide |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4163795A (en) | 1977-12-14 | 1979-08-07 | The Dow Chemical Company | Stabilized aqueous amide antimicrobial composition |
| US4163798A (en) * | 1977-12-14 | 1979-08-07 | The Dow Chemical Company | Stabilized aqueous amide antimicrobial composition |
| US4241080A (en) | 1979-05-29 | 1980-12-23 | The Dow Chemical Company | Stabilized aqueous antimicrobial composition |
| US4800082A (en) | 1987-03-23 | 1989-01-24 | The Dow Chemical Company | Sustained release microbiological control composition |
| CA2408643C (en) * | 2000-05-12 | 2011-01-11 | Omya Ag | Phenolate-containing formulation with low freezing point |
| RU2207154C1 (en) * | 2001-12-27 | 2003-06-27 | Общество с ограниченной ответственностью "МК ВИТА-ПУЛ" | Disinfecting detergent |
| AU2003210557A1 (en) * | 2002-01-17 | 2003-09-02 | Verichem, Inc. | Synergistic mixtures of o-phenylphenol and other microbiocides |
| US20040261196A1 (en) | 2003-06-27 | 2004-12-30 | The Procter & Gamble Company | Fabric care compositions for lipophilic fluid systems incorporating an antimicrobial agent |
| US20100096326A1 (en) * | 2007-01-22 | 2010-04-22 | Najmy Stephen W | Method to control reverse osmosis membrane biofouling in municipal water production |
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- 2010-09-27 WO PCT/US2010/050348 patent/WO2011038320A2/en not_active Ceased
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- 2010-09-27 BR BR112012004923A patent/BR112012004923A2/en not_active IP Right Cessation
- 2010-09-27 JP JP2012531094A patent/JP5744882B2/en not_active Expired - Fee Related
- 2010-09-27 US US13/388,469 patent/US8598234B2/en not_active Expired - Fee Related
- 2010-09-27 EP EP10760882.0A patent/EP2482652B1/en not_active Not-in-force
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|---|---|
| EP2482652B1 (en) | 2015-10-28 |
| BR112012004923A2 (en) | 2019-09-24 |
| CN102548401B (en) | 2014-11-05 |
| JP2013505958A (en) | 2013-02-21 |
| MX2012003734A (en) | 2012-04-30 |
| PL2482652T3 (en) | 2016-03-31 |
| WO2011038320A3 (en) | 2011-09-22 |
| EP2482652A2 (en) | 2012-08-08 |
| RU2536923C2 (en) | 2014-12-27 |
| US8598234B2 (en) | 2013-12-03 |
| US20120178818A1 (en) | 2012-07-12 |
| RU2012117605A (en) | 2013-11-10 |
| JP5744882B2 (en) | 2015-07-08 |
| CN102548401A (en) | 2012-07-04 |
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