Anti-microbial composition comprising a quaternary ammonium biocide and organopolysiloxane mixture
AssigneeByotrol PLC
InventorsUlrich Schwarz, Stephen Brian Falder
Life of this patent
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Abstract
The present invention provides an anti-microbial composition comprising (i) an antimicrobial agent with surfactant properties, (ii) a siloxane selected from those having the formulae V:(H3C)[SiO(CH3)2]nSi(CH3)3, and (H3C)[SiO(CH3)HnSi(CH3)3, and mixtures thereof, wherein n is from 1 to 24; and (iii) a polar solvent, wherein the ratio of (i) to (ii) is from about 100:1 to about 5:1.
Claims24
A method of substantially reducing or controlling the formation of microbial colonies on or at a hard surface or skin and providing a residual reduction or controlling effect on or at the hard surface or skin, the method comprising, applying to that hard surface or skin an anti-microbial composition comprising:
- (i) a quaternary ammonium compound having the formula R1R2R3R4N+X−,
- wherein R1, R2, R3 and R4 represent, independently a substituted or unsubstituted and/or straight chain or branched and/or interrupted or uninterrupted alkyl, aryl, alkylaryl, arylalkyl, cycloalkyl, heterocyclyl or alkenyl group or two or more of R1, R2, R3 and R4 together with the nitrogen atom form a substituted or unsubstituted heterocyclic ring, and wherein the total number of carbon atoms in the groups R1, R2, R3 and R4 is at least 4;
- wherein the substituents for the groups R1, R2, R3 and R4 are selected from the group consisting of alkyl, substituted alkyl, alkenyl, substituted alkenyl, heterocyclyl, substituted heterocyclyl, cycloalkyl, substituted cycloalkyl, aryl, substituted aryl, alkylaryl, substituted alkylaryl, arylalkyl, substituted arylalkyl, F, Cl, Br, I, —OR′, —NR′R″, —CF3, —CN,—NO2, —C2R′, —SR′, —N3, —C(═O)NR′R″, —NR′C(═O)R″, —C(═O)R′, —C(═O)OR′, —OC(═O)R′, —O(CR′R″)rC(═O)R′, —O(CR′R″)rNR″C(═O)R′, —O(CR′R″)rNR″SO2R′, —OC(═O)NR′R″, —NR′C(═O)OR″, —SO2R′, —SO2NR′R″, and —NR′SO2R″;
- wherein R′ and R″ are individually hydrogen, C1-8 alkyl, cycloalkyl, heterocyclyl, aryl, or arylalkyl, and r is an integer from 1 to 6, or R′ and R″ together form a cyclic functionality;
- wherein the term “substituted” as applied to alkyl, alkenyl, heterocyclyl, cycloalkyl, aryl, alkylaryl and arylalkyl refers to the substituents described above, starting with F and ending with —NR′SO2R″;
- and
- wherein if each R1, R2, R3 and R4 is an unsubstituted or uninterrupted alkyl, each of R1, R2, R3 and R4 is independently methyl or a C6-12 alkyl group;
- and wherein X− is halide or sulphonate;
- (ii) a siloxane selected from those having the formula (H3C)[SiO(CH3)2]nSi(CH3)3 and (H3C)[SiO(CH3)H]nSi(CH3)3 and mixtures thereof, wherein n is from 1 to 8;
- and
- (iii) a polar solvent;
- wherein the ratio of molecules of (i) to molecules of (ii) is from about 100:1 to about 5:1.
A method of preventing microorganisms from adhering and attaching to a hard surface or skin or reducing the number of microorganisms that adhere and attach to a hard surface or skin, the method comprising, applying to that hard surface or skin an anti-microbial composition comprising:
- (i) a quaternary ammonium compound having the formula R1R2R3R4N+X− wherein R1, R2, R3 and R4 represent, independently a substituted or unsubstituted and/or straight chain or branched and/or interrupted or uninterrupted alkyl, aryl, alkylaryl, arylalkyl, cycloalkyl, heterocyclyl or alkenyl group or two or more of R1, R2, R3 and R4 together with the nitrogen atom form a substituted or unsubstituted heterocyclic ring, and wherein the total number of carbon atoms in the groups R1, R2, R3 and R4 is at least 4;
- wherein the substituents for the groups R1, R2, R3 and R4 are selected from the group consisting of alkyl, substituted alkyl, alkenyl, substituted alkenyl, heterocyclyl, substituted heterocyclyl, cycloalkyl, substituted cycloalkyl, aryl, substituted aryl, alkylaryl, substituted alkylaryl, arylalkyl, substituted arylalkyl, F, Cl, Br, I, —OR′, —NR′R″, —CF3, —CN, —NO2, —C2R′, —SR′, —N3, —C(═O)NR′R″, —NR′C(═O)R″, —C(═O)R′, —C(═O)OR′,—O(CR′R″)rC(═O)R′, —O(CR′R″)rNR″C(═O)R′, —O(CR′R″)rNR″SO2R′, —OC(═O)NR′R″, —NR′C(═O)OR″, —SO2R′, —SO2NR′R″, and —NR′SO2R″;
- wherein R′ and R″ are individually hydrogen, C1-C8 alkyl, cycloalkyl, heterocyclyl, aryl, or arylalkyl, and r is an integer from 1 to 6, or R′ and R″ together form a cyclic functionality;
- wherein the term “substituted” as applied to alkyl, alkenyl, heterocyclyl, cycloalkyl, aryl, alkylaryl and arylalkyl refers to the substituents described above, starting with F and ending with —NR′SO2R″—;
- and
- wherein if each R1, R2, R3 and R4 is an unsubstituted or uninterrupted alkyl, each of R1, R2, R3 and R4 is independently methyl or a C6-12 alkyl group;
- and wherein X− is halide or sulphonate;
- (ii) a siloxane selected from those having the formula (H3C)[SiO(CH3)2]nSi(CH3)3 and (H3C)[SiO(CH3)H]nSi(CH3)3 mixtures thereof, wherein n is from 1 to 8;
- and
- (iii) a polar solvent;
- wherein the ratio of molecules of component (i) to molecules of component (ii) is from about 100:1 to about 5:1.
Dependencies are inferred from the claim text.