US2018237568A1PendingUtilityA1
Multifunctional polymers
Est. expiryApr 26, 2032(~5.8 yrs left)· nominal 20-yr term from priority
A01N 43/36C08F 220/60C08F 226/08C08F 226/10C08F 220/18C08F 220/1804
62
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Claims
Abstract
Described herein are multifunctional polymers comprising a first repeating unit having at least one pseudo-cationic moiety, a second repeating unit having at least a hydrophobic moiety, and a third repeating unit, where the weight-average molecular weight is less than about 10,000 Da. In one embodiment the polymers exhibit antimicrobial activity. Also provided are compositions formulated with the multifunctional polymers, and a method of providing antimicrobial activity.
Claims
exact text as granted — not AI-modified1 - 13 . (canceled)
14 . A terpolymer having structure
wherein:
R 1 and R 4 are independently selected from the group consisting of hydrogen, methyl, and combinations thereof,
R 2 and R 3 are independently selected C1-C20 alkyl,
R 5 is selected from the group consisting of functionalized and unfunctionalized alkyl, alkoxy, cycloalkyl, alkenyl, and aryl,
R 6 and R 7 are selected from the group consisting of functionalized and unfunctionalized alkyl, alkoxy, cycloalkyl, alkenyl, and aryl, and wherein R 6 and R 7 may form a 5 to 7-membered ring,
Q is selected from the group consisting of functionalized and unfunctionalized alkylene, alkyleneoxy, cycloalkylene, alkenylene, and arylene,
X is O, NH, or combinations thereof,
and a, b, and c are molar ratios equaling 100%.
15 . The terpolymer according to claim 14 wherein said a ranges from about 5% to about 80%, said b ranges from about 5% to about 60%, and said c ranges from about 5% to about 80% (all molar ratios).
16 . (canceled)
17 . The terpolymer according to claim 14 , wherein said terpolymer exhibits antimicrobial activity against a microbe selected from the group consisting of S. aureus, E. coli, P. aeruginosa, A. niger, C. albicans , and mixtures thereof.
18 - 21 . (canceled)
22 . A composition comprising a terpolymer having the structure:
wherein:
R 1 and R 4 are independently selected from the group consisting of hydrogen, methyl, and combinations thereof,
R 2 and R 3 are independently selected C1-C20 alkyl,
R 5 is selected from the group consisting of functionalized and unfunctionalized alkyl, alkoxy, cycloalkyl, alkenyl, and aryl,
R 6 and R 7 are selected from the group consisting of functionalized and unfunctionalized alkyl, alkoxy, cycloalkyl, alkenyl, and aryl, and wherein R 6 and R 7 may form a 5 to 7-membered ring,
Q is selected from the group consisting of functionalized and unfunctionalized alkylene, alkyleneoxy, cycloalkylene, alkenylene, and arylene,
X is O, NH, or combinations thereof,
and a, b, and c are molar ratios equaling 100%.
23 . The composition according to claim 22 that is a nutrition, food, beverage, pharmaceutical, cleaning, coating, paint, biocide, construction, energy, industrial, oilfield, personal care, household, performance, agricultural, pesticide, veterinary, fuel, lubricant, adhesive, electronic, textile, ink, or membrane composition.
24 . The composition according to claim 23 , wherein said personal care composition is a skin lotion, skin creme, skin ointment, skin salve, anti-aging creme, moisturizer, deodorant, tanning agent, sun block, sunscreen, foundation, concealer, eyebrow pencil, eye shadow, eye liner, mascara, rouge, finishing powder, lipstick, lip gloss, nail polish, make-up remover, nail polish remover, shampoo, rinse-off conditioner, leave-on conditioner, hair styling gel, hair mousse, hair spray, styling aide, hair color, or hair color remover.
25 . The composition according to claim 22 , wherein the terpolymer exhibits antimicrobial activity against a microbe selected from the group consisting of S. aureus, E. coli, P. aeruginosa, A. niger, C. albicans , and mixtures thereof.
26 . (canceled)
27 . A method of providing antimicrobial activity, said method comprising the step: contacting a composition with at least one terpolymer having the structure:
wherein:
R 1 and R 4 are independently selected from the group consisting of hydrogen, methyl, and combinations thereof,
R 2 and R 3 are independently selected C1-C20 alkyl,
R 5 is selected from the group consisting of functionalized and unfunctionalized alkyl, alkoxy, cycloalkyl, alkenyl, and aryl,
R 6 and R 7 are selected from the group consisting of functionalized and unfunctionalized alkyl, alkoxy, cycloalkyl, alkenyl, and aryl, and wherein R 6 and R 7 may form a 5 to 7-membered ring,
Q is selected from the group consisting of functionalized and unfunctionalized alkylene, alkyleneoxy, cycloalkylene, alkenylene, and arylene,
X is O, NH, or combinations thereof,
and a, b, and c are molar ratios equaling 100%.
28 . The method according to claim 27 that provides antimicrobial activity against a microbe selected from the group consisting of S. aureus, E. coli, P. aeruginosa, A. niger, C. albicans , and combinations thereof.
29 . The terpolymer according to claim 14 wherein said Q is C2-C20 alkylene.
30 . The composition according to claim 22 wherein in the terpolymer said Q is C2-C20 alkylene.
31 . The method according to claim 27 wherein in the terpolymer said Q is C2-C20 alkylene.
32 . The terpolymer according to claim 14 wherein said R 5 is C1-C20 alkyl.
33 . The composition according to claim 22 wherein in the terpolymer said R 5 is C1-C20 alkyl.
34 . The method according to claim 27 wherein in the terpolymer said R 5 is C1-C20 alkyl.Cited by (0)
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