IP Library Granted Patent US 9,675,065
Granted Patent B2
US 9,675,065 · App. 14/154,451 · Granted Jun 13, 2017

Biocide and bleach compositions and related methods

Inventor: Roy Martin (Downers Grove, IL)
Assignee: TRUOX, INC.
A01N37/02A01N43/08A01N59/00A23L3/3517A23L3/3544C02F1/50C02F2103/002
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Quick Facts
Patent No.
US 9,675,065
App. No.
14/154,451
Granted
Jun 13, 2017
Kind
B2
Abstract

Provided are biocide compositions and bleach compositions comprising organic acyl polyoxychlorine and related methods. The reduction of the acyl polyoxychlorine group releases a reactive intermediate that undergoes a series of cascading reduction steps, resulting in termination products Generally Recognized As Safe.

Claims (17)

1. A method of killing microorganisms comprising the steps of:

forming a biocide composition comprising a carrier and an organic acyl polyoxychlorine having the general formula;

wherein (X) is a polyoxychlorine selected from at least one of a chlorate having the general formula ClO 3 and perchlorate having the general formula ClO 4 ,

(R) comprises a C 1 to C 17 primary carbon based structure,

(n) is one or more; and

contacting the microorganisms with the composition, wherein the organic acyl polyoxychlorine experiences intracellular activation releasing oxychlorine intermediates.

2. The method according to claim 1 , further comprising controlling food-borne pathogenic bacteria by contacting the biocide composition with the bacteria.

3. The method according to claim 1 , further comprising applying the biocide composition for food intervention for the control of food-borne pathogenic bacteria.

4. The method according to claim 1 , further comprising applying the biocide composition to hard surfaces.

5. The method according to claim 1 , further comprising applying the biocide composition to recirculating systems.

6. The method according to claim 1 , wherein the primary carbon backbone (R) comprises an alkyl group.

7. The method according to claim 1 , wherein the primary carbon backbone (R) comprises an arylalkyl group.

8. The method according to claim 1 , wherein the primary carbon backbone (R) comprises a cycloalkyl group.

9. The method according to claim 1 , wherein the primary carbon backbone (R) comprises an aromatic group.

10. The method according to claim 1 , wherein the primary carbon backbone (R) comprises a heterocyclic group.

11. The method according to claim 1 , wherein the primary carbon backbone (R) comprises at least one C 1 to C 13 alkyl group.

12. The method according to claim 1 , wherein the primary carbon backbone (R) comprises at least one C 7 to C 11 alkyl group.

Continuity (7)
Division 13347854 · Jan 11, 2012
Continuation In Part 13066226 · Apr 8, 2011
Continuation In Part 13066199 · Apr 8, 2011
Continuation In Part 12932469 · Feb 25, 2011
Continuation In Part 12931896 · Feb 14, 2011
Related Publication 20150196027A1 · Jul 16, 2015
Related Publication 20170105412A9 · Apr 20, 2017