US2015025156A1PendingUtilityA1
Antimicrobial and foamable alcoholic compositions
Est. expiryFeb 24, 2032(~5.6 yrs left)· nominal 20-yr term from priority
A61P 31/02A61P 31/04A61P 17/00C07F 7/0829A01N 25/30A01N 25/16A01N 31/02
48
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Claims
Abstract
Antimicrobial and foamable alcoholic compositions, where the compositions include at least about 40 wt. % of a C 1-4 alcohol and one or more silane surfactants selected from (1) zwitterionic silane surfactants, (2) polyalkoxylated silane surfactants that contain at least one silane group and at least one polyalkylene oxide chain.
Claims
exact text as granted — not AI-modified1 . An antimicrobial alcoholic composition comprising:
at least about 40 weight percent of a C 1-4 alcohol or a mixture of two or more C 1-9 alcohols, based upon the total weight of the alcoholic composition; and one or more silane surfactants selected from (1) zwitterionic silane surfactants, (2) polyalkoxylated silane surfactants that contain at least one silane group and at least one polyalkylene oxide chain, and that are characterized by having a molecular weight distribution of less than about 2.4.
2 . The composition of claim 1 , wherein said alcohol comprises methanol, ethanol, propanol, isopropanol, butanol, isobutanol, tertiary butanol, or mixtures thereof.
3 . The composition of claim 1 , wherein said zwitterionic silane surfactant includes a polar ionic portion and a non-polar silane portion.
4 . The composition of claim 1 , wherein the zwitterionic surfactant may be represented by the formula
where wherein R 1 , R 2 , and R 3 are each independently a branched or linear C 2 to C 20 hydrocarbon group, R 7 is a divalent hydrocarbon group with about 4 to about 20 carbon atoms and optionally includes one or both of a lateral hydroxyl group and an ether oxygen, and R 9 is selected from the group consisting of
where R 4 , R 5 and R 8 are each independently alkyl groups with from 1 to about 6 carbon atoms.
5 . The composition of claim 1 , wherein said zwitterionic silane surfactant includes a polar dimethylglycine portion and a non-polar silane portion.
6 . The composition of claim 1 , wherein the zwitterionic surfactant may be represented by the formula
where each R is independently a branched or linear C 2 to C 20 hydrocarbon group, and wherein n is an integer from 1 to about 20.
7 . The composition of claim 1 , wherein said zwitterionic silane surfactant is represented by the formula
where n is an integer from 1 to about 20.
8 . The composition of claim 1 , wherein said composition further comprises at least one foam enhancer.
9 . The composition of claim 1 , wherein said silane surfactant is bis-PEG-18 methyl ether dimethyl silane.
10 . The composition of claim 1 , wherein the composition comprises at least about 50 wt. % of a C 1-4 alcohol, based upon the total weight of the alcoholic composition; and from about 0.001 to about 10 wt. % of one or more silane surfactants.
11 . The composition of claim 1 , wherein the composition comprises from about 0.001 to about 20 wt. % of one or more silane surfactants.
12 . The composition of claim 1 , wherein the molecular weight distribution (Mw/Mn) of the silane surfactant is less than about 2.2.
13 . The composition of claim 1 , wherein the molecular weight distribution (Mw/Mn) of the silane surfactant is less than about 2.0.
14 . The composition of claim 1 , wherein the molecular weight distribution (Mw/Mn) of the silane surfactant is less than about 1.8.
15 . The composition of claim 1 , wherein the composition comprises a primary foam enhancer that includes a poly(ethylene oxide)polymer, a poloxamer, hydroxyethyl cellulose, hydroxypropyl cellulose, or a combination thereof.
16 . The composition of claim 1 , wherein the composition comprises from 0 to about 10 wt. % of a primary foam enhancer that includes a poly(ethylene oxide)polymer, a poloxamer, hydroxyethyl cellulose, hydroxypropyl cellulose, or a combination thereof, based upon the total weight of the composition.
17 . A method of preparing a zwitterionic surfactant, the method comprising the steps of:
reacting an epoxide by means of an addition reaction in the presence of a hydrosilylation catalyst with a silane of the general formula
to form a silane-modified epoxide having an epoxide ring; and
reacting the silane-modified epoxide with an amine compound of the general formula
to form a betaine of the general formula
wherein R 1 , R 2 , and R 3 are each independently a branched or linear C 2 to C 20 hydrocarbon group, R 7 derives from the epoxide, and is a divalent hydrocarbon group with about 4 to about 20 carbon atoms and optionally includes a lateral hydroxyl group, and optionally includes an ether oxygen, and R 4 and R 5 are each independently selected from alkyl groups with 1 to about 6 carbon atoms.
18 . The method of claim 17 , wherein R 1 , R 2 , and R 3 are each n-butyl.Join the waitlist — get patent alerts
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