IP Library Granted Patent US 9,795,137
Granted Patent B2
US 9,795,137 · App. 14/391,749 · Granted Oct 24, 2017

Metalaxyl and prothioconazole cocrystals and methods of making and using

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Quick Facts
Patent No.
US 9,795,137
App. No.
14/391,749
Granted
Oct 24, 2017
Kind
B2
Abstract

The invention relates to co-crystals of metalaxyl and prothioconazole, to methods of making them, to compositions containing them and to the methods of using said co-crystals and said compositions to treat crops and plants.

Claims (23)

1. A cocrystal consisting of prothioconazole and metalaxyl, wherein said cocrystal has a water solubility less than the water solubility of metalaxyl alone.

2. The cocrystal of claim 1 , wherein said cocrystal has a melting point of about 100.8° when measured with a Differential Scanning Calorimeter.

3. The cocrystal of claim 1 , wherein the diameter of said cocrystal is about 0.1 μm to about 100 μm.

4. The cocrystal of claim 1 , wherein said cocrystal exhibits the Differential Scanning Calorimeter profile of FIG. 5 when crystallized from butyrolactone.

5. The cocrystal of claim 1 , wherein said cocrystal exhibits the Differential Scanning Calorimeter profile of FIG. 6 when crystallized from acetone.

6. A method of making the cocrystal of claim 1 comprising

(a) dissolving metalaxyl and prothioconazole in a solvent; and

(b) crystallizing the dissolved metalaxyl and prothioconazole,

wherein said cocrystal has a water solubility less than the water solubility of metalaxyl alone.

7. The method of claim 6 , wherein the dissolved metalaxyl and prothioconazole is crystallized in step (b) by the addition of water.

8. The method of claim 6 , wherein the dissolved metalaxyl and prothioconazole is crystallized in step (b) by freezing.

9. The method of claim 6 , wherein the dissolved metalaxyl and prothioconazole is crystallized in step (b) by seeding a solution with preformed metalaxyl and prothioconazole cocrystals.

10. The method of claim 6 , wherein said cocrystal has a melting point at about 100.8° when measured with a Differential Scanning Calorimeter.

11. A method of reducing damage or infestation to a crop caused by weeds, fungi, or pests by applying the cocrystal of claim 1 to said crop or its environment.

12. The method of claim 11 , wherein said cocrystal is applied to a crop from about 0.5 fluid ounces/acre to about 10.0 fluid ounces/acre.

13. The method of claim 11 , wherein said crop is selected from the group consisting of cereals, barley, wheat, winter wheat, triticale winter rye, ground nut, peanuts, rape, bulb onions, oilseed rape, canola, rice, pulses, soybeans, sugar beet, vegetables, and corn.

14. The method of claim 11 , wherein said cocrystal has a melting point of about 100.8° when measured with a Differential Scanning Calorimeter.

15. The method of claim 11 , wherein the diameter of said cocrystal is about 0.1 μm to about 100 μm.

16. A composition consisting essentially of the cocrystal as claimed in claim 1 .

17. The composition of claim 16 , wherein said composition consists essentially of about 0.01% to about 0.5%, about 1% to about 2%, about 2% to about 4%, about 5% to about 10%, or about 20% to about 50% percent by weight of said cocrystal.

18. A method of reducing damage or infestation to a crop caused by weeds, fungi, or pests by applying the composition according to claim 16 to said crop or its environment.

19. The composition of claim 16 , wherein the composition has a water solubility that is reduced by about 90% or more relative to a water solubility of metalaxyl alone.

20. The composition of claim 16 , wherein said composition consists essentially of about 0.1% to about 90% percent by weight of said cocrystal.

Assignments (2)
CHANGE OF ADDRESS Recorded May 7, 2021
From: BAYER CROPSCIENCE LP
To: BAYER CROPSCIENCE LP
Reel/Frame 056178/0211 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 16, 2014
From: FRIZZELL, DAVID
To: BAYER CROPSCIENCE LP
Reel/Frame 033959/0777 →