IP Library Granted Patent US 11,229,204
Granted Patent B2
US 11,229,204 · App. 16/971,746 · Granted Jan 25, 2022

Herbicidal composition comprising at least one phenolic active compound

Inventors: Sofiene Ben Kaab (Gembloux, BE); Haissam Jijakli (Scy, BE); Riadh Ksouri (Hammam-lif, TN); Olivier Parisi (Gembloux, BE); Simon Dal Maso (Mont-sur-Marchienne, BE)
Assignee: Université de Liège
A01N43/42A01N37/10
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 11,229,204
App. No.
16/971,746
Granted
Jan 25, 2022
Kind
B2
Abstract

The present invention relates to a herbicidal composition comprising at least one phenolic active compound being myricitrin. The invention also relates to the use of such a herbicidal composition.

Claims (33)

1. A method comprising:

applying an herbicidal composition including myricitrin to at least one of a part of a plant, a seed, or soil; and

obtaining phytotoxic activity including at least one of:

(a) inhibiting or preventing seed germination, or

(b) inhibiting or preventing at least one of:

(1) development and growth of roots,

(2) development and growth of hypocotyls,

(3) development and growth of epicotyls,

(4) development and growth of plantlets, or

(5) development and growth of aerial parts of the plant.

2. The method of claim 1 , wherein the myricitrin is:

from synthetic origin; or

from an extract or a fraction of an extract from at least one of roots, leaves, stems, fruits, seeds or flowers of at least one plant chosen from the group consisting of Limoniastrum guyonianum, Peganum harmala, Ruta chalepensis, Ricinus communis, Nitraria retusa, Cynara cardunculus, Artemisia herba - alba, Mesembryanthemum edule, Tamarix gallica, Datura stramonium, Myrica esculenta, Myrica cerifera, Nymphaea lotus, Nymphaea odorata, Chrysobalanus icaco, Polygonum aviculare and mixtures thereof.

3. The method of claim 1 , wherein the myricitrin is present in the herbicidal composition at a concentration ranging from 0.1 mg/L to 10000 mg/L.

4. The method of claim 1 , wherein the herbicidal composition includes at least one additional active compound chosen from the group consisting of syringic acid, p-coumaric acid, quercetin, naringenin, catechin, apigenin, gallic acid, cynarin acid, chlorogenic acid, cynaroside, luteolin, aguerin B, grosheimin, cynaropicrin and mixtures thereof.

5. The method of claim 4 , wherein the at least one additional active compound is:

from synthetic origin; or

from an extract or a fraction of an extract from at least one of roots, leaves, stems, fruits, seeds or flowers of at least one plant chosen from the group consisting of Limoniastrum guyonianum, Peganum harmala, Ruta chalepensis, Ricinus communis, Nitraria retusa, Cynara cardunculus, Artemisia herba - alba, Mesembryanthemum edule, Tamarix gallica, Datura stramonium, Myrica esculenta, Myrica cerifera, Nymphaea lotus, Nymphaea odorata, Chrysobalanus icaco, Polygonum aviculare and mixtures thereof.

6. The method of claim 4 , wherein the at least one additional active compound is present in the herbicidal composition at a concentration ranging from 0.1 mg/L to 10000 mg/L.

7. The method of claim 1 , wherein the herbicidal composition includes at least one solvent chosen from the group consisting of at least one natural lipophilic solvent, at least one synthetic lipophilic solvent, at least one natural hydrophilic solvent, at least one synthetic hydrophilic solvent, at least one natural amphiphilic solvent, at least one synthetic amphiphilic solvent and mixtures thereof.

8. The method of claim 7 , wherein the lipophilic solvent is chosen from the group consisting of animal oil, vegetable oil, petrochemical oil and mixtures thereof.

9. The method of claim 8 , wherein the vegetable oil is chosen from the group consisting of hazelnut oil, rapeseed oil, pine oil, soybean oil, sunflower oil, pistachio oil, olive oil, almond oil, sweet almond oil, peanut oil and mixtures thereof.

10. The method of claim 7 , wherein the hydrophilic solvent is chosen from the group consisting of water, alcohols, ketones, esters, ethers, polyols, ethyl acetate, propylene carbonate, acetonitrile and mixtures thereof.

11. The method of claim 7 , wherein at least one of the natural amphiphilic solvent or the synthetic amphiphilic solvent is at least one non-ionic surfactant.

12. The method of claim 11 , wherein the non-ionic surfactant is chosen from the group consisting of sorbitan monododecanoate poly(oxy-1,2-ethanediyl), alkyl polyglucosides, sorbitan laurate, polyoxyethylene (20) sorbitan monolaurate, polyoxyethylene (20) sorbitan monopalmitate, polyoxyethylene (20) sorbitan monostearate, polyoxyethylene (20) sorbitan monooleate, polyoxyethylene glycol sorbitan laurate, hexaethylene glycol sorbitan monooleate, polyoxyethylene sorbitan stearate, decaglyceryl monooleate, decaglyceryl dioleate, polyoxyethylene sorbitan tristearate, monodehydrosorbitol monooleate, sorbitan monolaurate, sorbitan monopalmitate, sorbitan laurate and mixtures thereof.

13. The method of claim 11 , wherein the non-ionic surfactant presents a hydrophilic-lipophilic balance (HLB) value between 5 and 7.

14. The method of claim 11 , wherein the non-ionic surfactant is present in the composition at a concentration ranging from 0.1 g/L to 500 g/L.

15. The method of claim 1 , wherein the herbicidal composition includes at least one of paraffin wax, 1-octyl-2-pyrrolidone, or and mixtures thereof.

16. The method of claim 1 , wherein the herbicidal composition is in the form of granules, liquids, emulsions or concentrates.

17. The method of claim 1 , wherein the myricitrin is present in the herbicidal composition at a concentration ranging from 1 mg/L to 100 mg/L.

18. The method of claim 4 , wherein the at least one additional active compound is present in the composition at a concentration ranging from 0.25 mg/L to 500 mg/L.

19. The method of claim 11 , wherein the non-ionic surfactant presents a hydrophilic-lipophilic balance (HLB) value equal to 6.

20. The method of claim 11 , wherein the non-ionic surfactant is present in the composition at a concentration ranging from 2 g/L to 25 g/L.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 13, 2021
From: BEN KAAB, SOFIENE; JIJAKLI, HAISSAM; KSOURI, RIADH; PARISI, OLIVIER; DAL MASO, SIMON
To: UNIVERSITÉ DE LIÈGE; FACULTÉ DES SCIENCES MATHÉMATIQUES, PHYSIQUES ET NATURELLES DE TUNIS; CENTRE DE BIOTECHNOLOGIE DE BORJ CEDRIA CBBC
Reel/Frame 057782/0903 →
Continuity (2)
Continuation PCTEP2018054418 · Feb 22, 2018
Related Publication 20200390097A1 · Dec 17, 2020