IP Library Granted Patent US 7,465,829
Granted Patent B2
US 7,465,829 · App. 10/369,175 · Granted Dec 16, 2008

Halo active aromatic sulfonamide organic compounds and uses therefor

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Quick Facts
Patent No.
US 7,465,829
App. No.
10/369,175
Granted
Dec 16, 2008
Kind
B2
Abstract

Halo active aromatic sulfonamide organic compounds have been known for over one hundred years. The ability of these compounds to releaser active halogen ions has been utilized in a range of biocidal and fungicidal applications. The most widely used sulfonamide organic compound for these applications has been Chloramine T. This invention deals with nearly discovered halo active aromatic sulfonamide organic compounds and uses of these compounds as biocides, odor control agents, bovine teat cleaners, drugs for cultured fish, soap biocides, stain removal agents, and paint fungicides.

Claims (55)

1. A process for eliminating the odor in an substrate which comprises the steps of treating the substrate with an effective amount of a solution of a halo active aromatic sulfonamide organic compound having the following structure;

Wherein,

R 1 is COOH,

X is chlorine, fluorine, bromine or iodine; and

M is sodium or potassium.

2. The process of claim 1 wherein,

M is sodium,

X is chlorine, and

R 1 is COOH.

3. A process for sanitizing the teats of a bovine which comprises applying to the teat of a solution containing an effective amount of a halo active aromatic sulfonamide organic compound having the following structure;

wherein,

X is a halogen;

R 1 is COOH; and

M is sodium or potassium.

4. A process for killing bacteria or fungi as may be contained on a substrate which comprises treating the substrate with an effective amount of a halo active aromatic sulfonamide organic compound having the following structure;

wherein,

R 1 is COOH or COOM,

X is chlorine and

M is sodium.

5. The process of claim 1 wherein the concentration of the halo active aromatic sulfonamide organic compound in the solution is from about 0.01 to about 20 weight percent.

6. The process of claim 1 wherein the concentration of the halo active aromatic sulfonamide organic compound in the solution is from about 0.1 to about 5 weight percent.

7. The process of claim 1 wherein the concentration of the halo active aromatic sulfonamide organic compound in the solution is from about 0.5 to about 1 weight percent.

8. The process of claim 2 wherein the concentration of the halo active aromatic sulfonamide organic compound in the solution is from about 0.01 to about 20 weight percent.

9. The process of claim 2 wherein the concentration of the halo active aromatic sulfonamide organic compound in the solution is from about 0.1 to about 5 weight percent.

10. The process of claim 2 wherein the concentration of the halo active aromatic sulfonamide organic compound in the solution is from about 0.5 to about 1 weight percent.

11. The process of claim 3 wherein the concentration of the halo active aromatic sulfonamide organic compound in the solution is from about 0.01 to about 20 weight percent.

12. The process of claim 3 wherein the concentration of the halo active aromatic sulfonamide organic in the solution is from about 0.1 to about 5 weight percent.

13. The process of claim 3 wherein the concentration of the halo active aromatic sulfonamide organic compound in the solution is from about 0.5 to about 1 weight percent.

14. The process of claim 4 wherein the concentration of the halo active aromatic sulfonamide organic compound in the solution is from about 0.01 to about 20 weight percent.

15. The process of claim 4 wherein the concentration of the halo active aromatic sulfonamide organic compound in the solution is from about 0.1 to about 5 weight percent.

16. The process of claim 4 wherein the concentration of the halo active aromatic sulfonamide organic compound in the solution is from about 0.5 to about 1 weight percent.

17. A process for curing cultural fish of bacterial infections which comprises allowing the diseased fish to swim for an effective period of time, in a solution containing an effective amount of an halo active aromatic sulfonamide organic compound having the following structure;

wherein,

X is halogen,

R 1 is COOH;

and M is sodium or potassium.

18. The process of claim 17 wherein the concentration of the halo active aromatic sulfonamide compound is from about 50 to about 600 ppm.

19. The process of claim 17 wherein the concentration of the halo active aromatic sulfonamide compound is from about 100 to about 400 ppm.

20. The process of claim 17 wherein the concentration of the halo active aromatic sulfonamide compound is from about 150 to about 250 ppm.

21. The process of claim 20 wherein the concentration of the halo active aromatic sulfonamide organic compound is about 200 ppm.

22. The process of claim 21 wherein the exposure time is about from about 10 to about 120 minutes.

23. The process of claim 22 wherein the exposure time is from about 30 to about 90 minutes.

24. A biocidal soap which contains an effective amount of a halo active aromatic sulfonamide compound having the following formula:

wherein,

R 1 is COOH or COOM,

X is chlorine, and

M is sodium.

25. The biocidal soap of claim 24 wherein the concentration of halo active aromatic sulfonamide organic compound is from about 0.1 to about 10 weight percent.

26. The biocidal soap of claim 25 wherein the concentration of halo active aromatic sulfonamide organic compound is from about 0.5 to about 2 weight percent.

27. The biocidal soap of claim 26 wherein the concentration of the halo active aromatic sulfonamide organic compound is about 0.75 weight percent.

28. A process for removing a stain, as contained on a textile substrate which comprises treating the substrate with an effective amount of a halo active aromatic sulfonamide organic compound having the following structure;

wherein,

X is a halogen,

R 1 is COOH; and

M is sodium or potassium.

Assignments (4)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 31, 2018
From: SCHNEIDER, CHARLES A.
To: SCHNEIDER, DAVID J.
Reel/Frame 044784/0393 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 18, 2013
From: SCHNEIDER ADVANCED TECHNOLOGIES, INC.
To: SCHNEIDER, CHARLES A.; SCHNEIDER, DAVID J.
Reel/Frame 031432/0921 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 2, 2006
From: H&S CHEMICAL CO. INC.
To: SCHNEIDER ADVANCED TECHNOLOGIES, INC.
Reel/Frame 017105/0453 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 18, 2003
From: SCHNEIDER, CHARLES A.; SCHNEIDER, DAVID J.
To: H + S CHEMICAL COMPANY, INC.
Reel/Frame 013795/0004 →