US2018228151A1PendingUtilityA1
Encapsulated lactams
Assignee: CONOPCO INC A/B/A UNILEVERPriority: Aug 20, 2015Filed: Jul 25, 2016Published: Aug 16, 2018
Est. expiryAug 20, 2035(~9.1 yrs left)· nominal 20-yr term from priority
A61Q 11/00A01N 25/02A01N 43/36A61K 8/11A61Q 17/005A01N 25/04A61K 8/87A01N 25/26A61K 8/4913A61Q 5/02
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Claims
Abstract
Encapsulated lactams suitable for use in compositions and compositions comprising encapsulated lactams. The compositions may be useful as antimicrobial, anti-biofilm and bacteriostatic compositions. Methods of encapsulating lactams.
Claims
exact text as granted — not AI-modified1 . An encapsulated lactam wherein the lactam is a lactam of Formula Ia or Formula IIa:
wherein R is H, halogen, or C 1-4 alkyl; characterised in that encapsulated lactam is encapsulated in a condensation polymer.
2 . The encapsulated lactam of claim 1 , wherein R is H, F, Cl, Br, or Me.
3 . The encapsulated lactam of claim 1 , wherein the lactam is selected from:
4 . The encapsulated lactam of claim 1 wherein the lactam is encapsulated in a polymer selected from a poly urea polymer, a melamine-formaldehyde copolymer; a urea formaldehyde copolymer and mixtures thereof.
5 . The encapsulated lactam of claim 1 wherein the lactam is encapsulated in a polymer formed from polymethylene polyphenyl isocyanate and hexamethylenediamine.
6 . An additive comprising an encapsulated lactam according to claim 1 in a carrier oil.
7 . The additive of claim 6 , wherein the carrier oil is an alkyl ketone, optionally wherein the carrier oil is heptan-2-one.
8 . A composition comprising an encapsulated lactam according to claim 1 .
9 . The composition of claim 8 , wherein the composition contains 0.000001 to 50% wt. lactam, optionally 0.001 to 50% wt., optionally 0.01 to 5% wt, optionally 0.01-2%.
10 . A method of encapsulating a lactam, wherein the lactam is a lactam of Formula Ia or Formula IIa:
wherein R is H, halogen, or C 1-4 alkyl,
the method comprising:
(a) combining said lactam with a carrier oil; then
(b) combining said lactam in carrier oil with a first polymerisation agent; then
(c) combining the product of step (b) with an aqueous solution of a stabilizer;
(d) adding an aqueous solution comprising a second polymerization agent to the product of step (c) while stirring the mixture;
wherein the first and second polymerization agents form a polymer when they react with each other.
11 . The method of claim 10 , wherein step (a) comprises dissolving said lactam in an alkyl ketone to form a solution, optionally wherein the alkyl ketone is heptan-2-one and/or optionally wherein the concentration of the solution is less than 1% wt.
12 . The method of claim 10 , wherein the first polymerization agent is an isocyanate, optionally polymethylene polyphenyl isocyanate.
13 . The method of claim 10 , wherein the second polymerization agent is an α,ω-diamino C 2-10 alkylene; optionally hexamethylenediamine.
14 . The method of claim 10 , wherein the method further comprising the step of agitating the product of step (d) for at least one 1 hour; optionally around 5 hours.Cited by (0)
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