Microbicidal composition

Information

  • Patent Grant
  • 11849726
  • Patent Number
    11,849,726
  • Date Filed
    Monday, September 25, 2017
    6 years ago
  • Date Issued
    Tuesday, December 26, 2023
    6 months ago
  • CPC
  • Field of Search
    • CPC
    • A61N31/14
  • International Classifications
    • A01N31/14
    • Term Extension
      21
Abstract
The invention is directed to a synergistic microbicidal composition having two components: phenoxyethanol and dipropylene glycol phenyl ether and a method for inhibiting growth of microbes using the same.
Description

This invention relates to microbicidal compositions containing 2-phenoxyethanol and dipropylene glycol phenyl ether.


A composition containing 5-chloro-2-methylisothiazolin-3-one, 2-methylisothiazolin-3-one and a nonionic dispersant is disclosed in U.S. Pat. No. 4,295,932. The composition contains a 3:1 mixture of 5-chloro-2-methylisothiazolin-3-one and 2-methylisothiazolin-3-one, and a copolymer of ethylene oxide and propylene oxide which appears to have the same composition as PLURONIC L61 or TERGITOL L61 dispersant. However, there is a need for combinations of microbicides having synergistic activity against various strains of microorganisms to provide effective control of the microorganisms. Moreover, there is a need for such combinations containing lower levels of individual microbicides for environmental and economic benefit. The problem addressed by this invention is to provide such synergistic combinations of microbicides.


STATEMENT OF THE INVENTION

The present invention is directed to a synergistic microbicidal composition comprising phenoxyethanol and dipropylene glycol phenyl ether.


The present invention is further directed to a method for inhibiting the growth of microorganisms in an aqueous medium; said method comprising adding to the aqueous medium phenoxyethanol and dipropylene glycol phenyl ether wherein the weight ratio of phenoxyethanol to dipropylene glycol phenyl ether is from 1:0.01 to 1:27.







DETAILED DESCRIPTION OF THE INVENTION

“Phenoxyethanol” is 2-phenoxy-1-ethanol (CAS No. 122-99-6). Dipropylene glycol phenyl ether is the compound with CAS No. 51730-94-0. As used herein, the following terms have the designated definitions, unless the context clearly indicates otherwise. The term “microbicide” refers to a compound capable of inhibiting the growth of or controlling the growth of microorganisms; microbicides include bactericides, fungicides and algaecides. 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=milliliter. Unless otherwise specified, temperatures are in degrees centigrade (° C.), references to percentages are percentages by weight (wt %) and amounts and ratios are on an active ingredient basis.


In the present invention a synergistic antimicrobial composition is formed by combining phenoxyethanol and dipropylene glycol phenyl ether. Synergy between phenoxyethanol and dipropylene glycol phenyl ether is demonstrated over the range of 1:0.01 and 1:27.


Preferably, each of the synergistic microbicidal compositions is substantially free of microbicides other than to dipropylene glycol phenyl ether and phenoxyethanol, i.e., it has less than 1 wt % of microbicides other than to dipropylene glycol phenyl ether and phenoxyethanol based on total weight of active ingredients, preferably less than 0.5 wt %, preferably less than 0.2 wt %, preferably less than 0.1 wt %. Preferably, when the dipropylene glycol phenyl ether and phenoxyethanol are added to an aqueous medium, the medium is substantially free of other microbicides, i.e., it has less than 1 wt % of microbicides other than the dipropylene glycol phenyl ether and phenoxyethanol based on total weight of active ingredients, preferably less than 0.5 wt %, preferably less than 0.2 wt %, preferably less than 0.1 wt %.


The compositions of this invention may contain other ingredients, e.g., defoamers and emulsifiers. The microbicidal compositions of the present invention can be used to inhibit the growth of microorganisms or higher forms of aquatic life (such as protozoans, invertebrates, bryozoans, dinoflagellates, crustaceans, mollusks, etc) by introducing a microbicidally effective amount of the compositions into an aqueous medium subject to microbial attack. Suitable aqueous media are found in, for example: industrial process water; electrocoat deposition systems; cooling towers; air washers; gas scrubbers; mineral slurries; wastewater treatment; ornamental fountains; reverse osmosis filtration; ultrafiltration; ballast water; evaporative condensers; heat exchangers; pulp and paper processing fluids and additives; starch; plastics; emulsions; dispersions; paints; latices; coatings, 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; personal care products such as wipes, lotions, sunscreen, conditioners, creams, and other leave-on applications; detergents; industrial cleaners; floor 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; agriculture adjuvant preservation; surfactant preservation; medical devices; diagnostic reagent preservation; food preservation, such as plastic or paper food wrap; food, beverage, and industrial process pasteurizers; toilet bowls; recreational water; pools; and spas.


The specific amount of the microbicidal compositions of this invention necessary to inhibit or control the growth of microorganisms in an application will vary. Typically, the amount of the composition of the present invention is sufficient to control the growth of microorganisms if it provides from 1,000 to 30,000 ppm (parts per million) active ingredients of the composition. It is preferred that the active ingredients (i.e., dipropylene glycol phenyl ether and phenoxyethanol) of the composition be present in the medium to be treated in an amount of at least 2,000 ppm, preferably at least 3,000 ppm, preferably at least 4,000 ppm. It is preferred that the active ingredients of the composition be present in the locus in an amount of no more than 16,000 ppm, preferably no more than 14,000 ppm, preferably no more than 12,000 ppm, preferably no more than 10,000 ppm, preferably no more than 8,000 ppm, preferably no more than 7,000 ppm. In a method of this invention, a composition is treated to inhibit microbial growth by adding, together or separately, the nonionic surfactant and phenoxyethanol, in amounts that would produce the concentrations indicated above.


Examples

Phenoxyethanol and Dipropylene glycol phenyl ether were evaluated for synergy by determining the synergy index (S.I.) of the combination. Synergy index was calculated based on minimum inhibitory concentrations (MIC) of two antimicrobial compounds (A and B) alone and in combinations. The MIC test were run in accordance with the method described in U.S. Pat. No. 9,034,905. The tests organisms were Gram negative bacteria (Pseudomonas aeruginosa ATCC #15442), Gram positive bacteria (Staphylococcus aureus ATCC #6538), and yeast (Candida albicans ATCC #10231) and mold (Aspergillus brasiliensis ATCC #16404). Contact time for the bacteria was 24 and 48 hours, yeast was 48 and 72 hrs, and 3 and 7 days for mold. The test was carried out in 96 well microtiter plates. More details on the tests are shown in Tables 1-4.









TABLE 1







Products tested








Solvent
Trade name





Phenoxyethanol
Neolone PH100 ™



Commercially available from



The Dow Chemical Company, Midland,



MI


Dipropylene glycol phenyl ether
Dowanol DiPPh ™



Commercially available from



The Dow Chemical Company, Midland,



MI
















TABLE 2







Inoculums Used


Inoculum Size of organisms (CFU/ml)











Staphylococcus


Pseudomonas


Aspergillus


Candida




aureus


aeruginosa


brasiliensis


albicans



ATCC# 6538
ATCC # 15442
ATCC# 16404
ATCC#10231





1.2E+06
1.2E+06
3.1E+04
4.7E+04
















TABLE 3







Media Used


Media Used for testing











Staphylococcus


Pseudomonas


Aspergillus


Candida




aureus


aeruginosa


brasiliensis


albicans



ATCC# 6538
ATCC # 15442
ATCC# 16404
ATCC#10231





10% Tryptic soy
10% Tryptic soy
Potato dextrose
Potato dextrose


broth
broth
broth
broth









The test results for demonstration of synergy of the MIC combinations are shown in Table 4. Each Table shows the combinations of two components results against the microorganisms tested with incubation times; the end-point activity in ppm measured by the MIC for compound A alone (CA), for component B alone (CB), and the mixture (Ca) and (Cb); the calculated SI value; and the range of synergistic ratios for each combination tested. SI is calculated as follows:

Ca/CA+Cb/CB=Synergy Index (“SI”)

Wherein:

    • CA=concentration of compound A 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.
    • CB=concentration of compound B in ppm, acting alone, which produced an end point (MIC of Compound B).
    • Cb=concentration of compound B in ppm, in the mixture, which produced an end point.


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.


Only synergistic ratios or ratios which reduce the use level of either component are illustrated in the table 4.









TABLE 4







Ca: component in ppm AI of NeolonePH100 (Phenoxyethanol)


Cb: component in ppm AI of Dowanol DiPPh (Dipropylene


glycol phenyl ether)


Ratio: Ca:Cb












Test
Contact






Organisms
Time
Ca
Cb
S.I.
Ca:Cb
















A. brasiliensis

 3 days
3000
0




ATCC #

0
10000




16404

2500
20
0.84
1:0.01




2500
30
0.84
1:0.01




2500
40
0.84
1:0.02




2500
50
0.84
1:0.02




2500
60
0.84
1:0.02




2500
100
0.84
1:0.04




2500
200
0.85
1:0.08




2500
300
0.86
1:0.12




2500
400
0.87
1:0.16




2500
500
0.88
1:0.20




2500
600
0.89
1:0.24




2500
800
0.91
1:0.32




2500
1000
0.93
1:0.40




2500
2000
1.03
1:0.80




2000
80
0.67
1:0.04




2000
100
0.68
1:0.05




2000
200
0.69
1:0.10




2000
300
0.70
1:0.15




2000
400
0.71
1:0.20




2000
500
0.72
1:0.25




2000
600
0.73
1:0.30




2000
800
0.75
1:0.40




2000
1000
0.77
1:0.50




2000
2000
0.87
1:1.00




2000
3000
0.97
1:1.50




2000
4000
1.07
1:2.00




1000
1000
0.43
1:1.00




1000
2000
0.53
1:2.00




1000
3000
0.63
1:3.00




1000
4000
0.73
1:4.00




1000
5000
0.83
1:5.00




1000
6000
0.93
1:6.00




1000
8000
1.13
1:8.00




750
2000
0.45
1:2.67




750
3000
0.55
1:4.00




750
4000
0.65
1:5.33




750
5000
0.75
1:6.67




750
6000
0.85
1:8.00




750
8000
1.05
 1:10.67




500
4000
0.57
1:8.00




500
5000
0.67
 1:10.00




500
6000
0.77
 1:12.00




500
8000
0.97
 1:16.00




400
4000
0.53
 1:10.00




400
5000
0.63
 1:12.50




400
6000
0.73
 1:15.00




400
8000
0.93
 1:20.00




300
4000
0.50
 1:13.33




300
5000
0.60
 1:16.67




300
6000
0.70
 1:20.00




300
8000
0.90
 1:26.67



C. albicans

24 hrs
5000
0




ATCC #

0
19992




10231

4000
300
0.82
1:0.08




4000
400
0.82
1:0.10




4000
600
0.83
1:0.15




4000
800
0.84
1:0.20




4000
1000
0.85
1:0.25




4000
2000
0.90
1:0.50




4000
3000
0.95
1:0.75




4000
4000
1.00
1:1.00




3000
800
0.64
1:0.27




3000
1000
0.65
1:0.33




3000
2000
0.70
1:0.67




3000
3000
0.75
1:1.00




3000
4000
0.80
1:1.33




3000
6002
0.90
1:2.00




3000
8004
1.00
1:2.67




2500
500
0.53
1:0.20




2500
600
0.53
1:0.24




2500
800
0.54
1:0.32




2500
1000
0.55
1:0.40




2500
2000
0.60
1:0.80




2500
3000
0.65
1:1.20




2500
4000
0.70
1:1.60




2500
6000
0.80
1:2.40




2500
8000
0.90
1:3.20




2500
10000
1.00
1:4.00




2000
3000
0.55
1:1.50




2000
4000
0.60
1:2.00




2000
6000
0.70
1:3.00




2000
8000
0.80
1:4.00




2000
10000
0.90
1:5.00




1000
4000
0.40
1:4.00




1000
6000
0.50
1:6.00




1000
8000
0.60
1:8.00




1000
10000
0.70
 1:10.00




750
4000
0.35
1:5.33




750
6000
0.45
1:8.00




750
8000
0.55
 1:10.67




750
10000
0.65
 1:13.33




500
4000
0.30
1:8.00




500
6000
0.40
 1:12.00




500
8000
0.50
 1:16.00




500
10000
0.60
 1:20.00



S. aureus

24 hrs
5000
0




ATCC#6538

0
19992






3000
3998
0.80
1:1.33




3000
4997
0.85
1:1.67




3000
6002
0.90
1:2.00




3000
8004
1.00
1:2.67




2500
3998
0.70
1:1.60




2500
4997
0.75
1:2.00




2500
6002
0.80
1:2.40




2500
8004
0.90
1:3.20




2500
9999
1.00
1:4.00








Claims
  • 1. A synergistic microbicidal composition comprising phenoxyethanol and dipropylene glycol phenyl ether.
  • 2. The synergistic microbicidal composition of claim 1, wherein the weight ratio of phenoxyethanol to dipropylene glycol phenyl ether is from 1:0.01 to 1:27.
PCT Information
Filing Document Filing Date Country Kind
PCT/US2017/053203 9/25/2017 WO
Publishing Document Publishing Date Country Kind
WO2018/063971 4/5/2018 WO A
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20070007811 Chung Jan 2007 A1
20110318494 Donate Dec 2011 A1
20120009176 Ji et al. Jan 2012 A1
20130136709 Pillai et al. May 2013 A1
20130231397 Beilfuss et al. Sep 2013 A1
20130277279 Marques et al. Oct 2013 A1
20160219875 Gandhi et al. Aug 2016 A1
Non-Patent Literature Citations (1)
Entry
Lucchini, et al., “Antibacterial activity of phenolic compounds and aromatic alcohols”, Res. in Microbiol., vol. 141, No. 4, pp. 499-510 (1990).
Related Publications (1)
Number Date Country
20200205405 A1 Jul 2020 US
Provisional Applications (1)
Number Date Country
62402769 Sep 2016 US