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| United States Patent | 4005193 |
| Link to this page | http://www.wikipatents.com/4005193.html |
| Inventor(s) | Green; Harold A. (Havertown, PA);
Merianos; John J. (Jersey City, NJ);
Petrocci; Alfonso N. (Glen Rock, NJ) |
| Abstract | Water-in-oil emulsions containing a polymeric quaternary ammonium compound
prepared by the condensation of 1,4-dihalo-2-butene and
1,4-bis-dimethylamino-2-butene as a biocidal agent, and wherein the
emulsifying agent is an amine oxide. |
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Title Information  |
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| Publication Date |
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January 25, 1977 |
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| Filing Date |
October 20, 1975 |
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| Parent Case |
This is a continuation-in-part of application Ser. No. 495,328, filed Aug.
7, 1974 and issued as U.S. Pat. No. 3,929,990, dated Dec. 30, 1975, which
was, in turn, a continuation-in-part of application Ser. No. 425,931,
filed Dec. 18, 1973, now issued as U.S. Pat. No. 3,874,870, dated Apr. 1,
1975. |
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Title Information  |
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Description  |
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This invention relates to water-in-oil emulsions which contain a polymeric
quaternary ammonium compound as a anti-fungal agent, and it particularly
relates to such emulsions wherein the emulsifying agent is an amine oxide.
The aforesaid application Ser. No. 425,931, disclosed that the polymeric
quaternary ammonium compound formed by the condensation of
1,4-dihalo-2-butene and 1,4-bis-dimethylamino-2-butene comprises a very
potent biocidal agent in oil-in-water emulsions and that such emulsions
have relatively little foaming action.
As disclosed in the aforesaid application Ser. No. 425,931, which is
herewith incorporated by reference, the aforesaid polymeric quaternary
ammonium compound is formed by mixing 1,4-dihalo-2-butene and
1,4-bis-dimethylamino-2-butene dissolved in a solvent, in relative molar
proportions of between about 1:3 and about 3:1, at room temperature,
whereby an exothermic reaction is obtained causing the temperature of the
mixture to rise, then maintaining the mixture at no higher than reflux
temperature until the reaction is complete. For the sake of brevity, this
compound will be referred to as "Product P".
This same polymeric quaternary ammonium compound provides the same
satisfactory results when used in water-in-oil emulsions, except when such
water-in-oil emulsions include non-ionic emulsifiers. When such non-ionic
emulsifiers are present, biocidal effectiveness is seriously impaired.
However, when the non-ionic emulsifier is replaced by an amine oxide as
the emulsifying agent, the biocidal effectiveness is satisfactory.
In the same manner as the oil-in-water emulsions described in the aforesaid
parent application, the compound in the present water-in-oil emulsions is
active at concentrations as low as 10 ppm against Aerobacter aerogenes and
as low as 25 ppm against Pseudomonas aeruginosa, while against algae, such
as Chlorella pyrenoidosa, it is active at a concentration at least as low
as 1 ppm or lower, and it is active against a mixture of the fungi
Aspergillis niger and Penicillium expansum in concentrations of about 2000
ppm, or less, as a inhibitor against proliferation. Insofar as concerns
their upper limits, the concentration appears to be capable of being
increased indefinitely without deleteriously affecting the biocidal
activity.
Also, as in the case of the corresponding oil-in-water emulsions described
in the aforesaid parent application, when used in cosmetic compositions
the present water-in-oil emulsions are effectively protected by the
polyquaternary compound.
In order to show anti-fungal activity of water-in-oil emulsions, utilizing
the present polymeric quaternary ammonium compound, wherein an amine oxide
is used as the emulsifying agent, a cosmetic-type water-in-oil emulsion
was prepared using an emulsion containing an amine oxide, namely "Ammonyx
SO", as the emulsifier. "Ammonyx SO" is stearyldimethylamine-N-oxide made
by the Onyx Chemical Company, Jersey City, N.J.
The amine oxide, "Ammonyx SO" is dissolved in water, together with "Product
P", at 65.degree. to 75.degree. C. Then, the lanolin, petrolatum and
mineral oil are heated to a homogeneous melt at between 65.degree. to
75.degree. C. Thereafter, with constant mechanical stirring, the aqueous
phase is added very slowly to the oil phase and stirring is continued
while cooling, until a stable smooth emulsion results.
The following tables illustrate the particular compositions used and the
anti-fungal results achieved with each composition:
Table 1
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The following emulsions were prepared for microbiological
testing:
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Emulsion
Emulsion Emulsion
A B C
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Lanolin, USP Anhydrous
2.0 2.0 2.0
Mineral oil (65/76 saybolt)
40.0 40.0 40.0
Petrolatum, White USP
30.0 30.0 30.0
"Ammonyx SO" (25%)
16.0 16.0 16.0
"Product P" 1.0 0.5 0.2
Water 11.0 11.5 11.8
Emulsion
Emulsion
D E
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Lanolin, USP Anhydrous
2.0 1.0
Mineral oil (65/75 saybolt)
40.0 35.0
Petrolatum, White USP
30.0
"Ammonyx SO" 16.0 10.0
"Product P" 0.0 0.2
Cetyl Alcohol 1.0
Water 12.0 52.8
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Emulsions A, B, C and D are water-in-oil emulsions containing "Product P"
in concentrations of 10,000 ppm; 5,000 ppm; 2,000 ppm; and 0 ppm
respectively.
Emulsion E is an oil-in-water emulsion of "Product P", which has been shown
to be a potent fungicidal emulsion.
Emulsion D is a "negative" control for emulsions A, B, C and emulsion E is
a "positive" control for emulsions A, B, and C.
Following is a description of the method used in testing for the
anti-fungal properties of water-in-oil emulsions.
Fifty gram samples of each emulsion to be tested were aseptically
transferred to sterile 8 ounce wide-mouth jars. Two replicate jars and an
untreated control were prepared in each instance.
Each jar was inoculated with 5.0 ml. of an aqueous suspension of
Aspergillis niger, and Penicillium expansum to provide a concentration of
1 .times. 10.sup.5 spores per ml. of jar content. (The spore suspension
was prepared previously as an aqueous suspension of 14 day old agar growth
of test organisms).
At weekly intervals following inoculation, some of the jar contents in
sterile "Azolectin"-"Tween 80" sterile neutralizer solutions were plated
into Sabouraud Dextrose agar, incubated at 28.degree. C, and observed at 7
and 14 days following the plating, to count the number of colonies arising
from the viable spores.
Table 2
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Number of Spores Counted
Start Week 1 Week 2 Week 3 Week 4
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Emulsion A
1 .times. 10.sup.5
2 .times. 10.sup.3
16 .times. 10.sup.1
8 .times. 10.sup.1
6 .times. 10.sup.1
Emulsion B
1 .times. 10.sup.5
5 .times. 10.sup.3
42 .times. 10.sup.1
64 .times.10.sup.1
45 .times. 10.sup.1
Emulsion C
1 .times. 10.sup.5
9 .times. 10.sup.3
63 .times. 10.sup.1
86 .times. 10.sup.1
14 .times. 10.sup.1
Emulsion D
1 .times. 10.sup.5
2 .times. 10.sup.5
34 .times. 10.sup.4
13 .times. 10.sup.4
18 .times. 10.sup.4
Emulsion E
1 .times. 10.sup.5
<10 <10 <10 <10
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The biocidal test results displayed in Tables 1 and 2 clearly indicate that
the polyquaternary compound functions as an effective anti-fungal agent in
water-in-oil emulsions when it is in a system which is emulsified by amine
oxide emulsifiers.
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