IP Library Granted Patent US 8,968,723
Granted Patent B2
US 8,968,723 · App. 13/716,483 · Granted Mar 3, 2015

Chemical and biological agents for the control of molluscs

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Quick Facts
Patent No.
US 8,968,723
App. No.
13/716,483
Granted
Mar 3, 2015
Kind
B2
Abstract

Compositions and methods for controlling molluscs, members of the Gastropoda and Bivalvia classes which includes but is not limited to lactones, lactams, carbamates, amides, and/or carboxylic acid containing compounds as active ingredients and/or compounds derived from Pseudomonas and/or Erwinia . Also provided are methods and compositions for increasing the efficacy of chemical and biological control for invasive molluscs in open waters, power plants, and drinking water treatment facilities under coldwater conditions.

Claims (11)

1. A method for controlling one or more molluscs comprising:

introducing lactone and kaolinite in a body of water or a solid surface of pipes made of iron and/or polyvinyl chloride, in amounts effective for controlling said molluscs, wherein said lactone for controlling molluscs is present in an amount to result in at least 20% mortality of said molluscs relative to untreated control and said kaolinite is present in an amount sufficient to increase mortality rate of said lactone for controlling molluscs by at least 20%.

2. A method for controlling one or more molluscs comprising:

introducing lactone and kaolinite in a body of water or a solid surface of pipes made of iron and/or polyvinyl chloride, in amounts effective for controlling said molluscs.

3. The method according to claim 1 , wherein said lactone has a hydroxylated unsaturated lactone structure comprising at least one lactone moiety which is a 5 membered γ-lactone, at least one unsaturated moiety and at least one alcohol group;

a molecular weight from 285 to about 310 in the core structure; and at least 15 carbons and at least 3 oxygens.

4. The method according to claim 1 , wherein said lactone is selected from the group consisting of gamma-dodecalactone, delta-tridecalactone, piliferolide A and alpha-heptyl-gamma-butyrolactone.

5. The method according to claim 1 , wherein said lactone are derived from a Pseudomonas fluorescens or cell suspension from Pseudomonas fluorescens.

6. The method according to claim 2 , wherein said lactone has a hydroxylated unsaturated lactone structure comprising at least one lactone moiety which is a 5 membered γ-lactone, at least one unsaturated moiety and at least one alcohol group; a molecular weight from 285 to about 310 in the core structure; and at least 15 carbons and at least 3 oxygens.

7. The method according to claim 2 , wherein said lactone is selected from the group consisting of gamma-dodecalactone, delta-tridecalactone, piliferolide A and alpha-heptyl-gamma-butyrolactone.

8. The method according to claim 2 , wherein said lactone are derived from a Pseudomonas fluorescens or cell suspension from Pseudomonas fluorescens.

Assignments (4)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 28, 2026
From: WILMINGTON SAVINGS FUND SOCIETY, FSB
To: PFG HOLDING CORPORATION
Reel/Frame 075515/0294 →
RELEASE OF SECURITY INTEREST Recorded Aug 10, 2022
From: IVY INVESTMENT MANAGEMENT COMPANY
To: PRO FARM GROUP, INC.
Reel/Frame 061067/0536 →
INTELLECTUAL PROPERTY SECURITY AGREEMENT Recorded Aug 21, 2015
From: MARRONE BIO INNOVATIONS, INC.
To: IVY INVESTMENT MANAGEMENT COMPANY
Reel/Frame 036420/0429 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 23, 2015
From: ASOLKAR, RATNAKAR; RACKL, SARAHANN; HUANG, HUAZHANG; KOIVUNEN, MARJA; MARRONE, PAMELA
To: MARRONE BIO INNOVATIONS, INC.
Reel/Frame 035007/0831 →