IP Library Granted Patent US 8,158,559
Granted Patent B2
US 8,158,559 · App. 13/053,499 · Granted Apr 17, 2012

Herbicidal combination comprising dimethoxytriazinyl-substituted difluoromethanesulfonylanilides

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Quick Facts
Patent No.
US 8,158,559
App. No.
13/053,499
Granted
Apr 17, 2012
Kind
B2
Abstract

The present invention relates to a herbicide combination comprising components (A) and (B) where (A) denotes one or more compounds or salts thereof from the group described by the general formula (I): in which R 1 is halogen, preferably fluorine or chlorine, R 2 is hydrogen and R 3 is hydroxyl or R 2 and R 3 together with the carbon atom to which they are attached are a carbonyl group C═O and R 4 is hydrogen or methyl; and (B) denotes one or more herbicides from the group of the pyrimidines consisting of: (B1-1) ancymidol, (B1-2) flurprimidol, (B1-3) pyrimisulfan, (B2-1) bispyribac-sodium, (B2-2) pyribenzoxim, (B2-3) pyriminobac-methyl, (B2-4) pyribambenz-isopropyl, (B2-5) pyribambenz-propyl, (B3-1) pyriftalid, (B3-2) pyrithiobac-sodium, (B4-1) benzfendizone, (B4-2) bromacil, (B4-3) butafenacil, (B4-4) lenacil, (B4-5) terbacil, (B4-6) SYN-523, (B4-7) saflufenacil.

Claims (28)

1. A herbicide combination comprising

(A) a compound of formula (A1) or salt thereof

 and

(B) saflufenacil.

2. The herbicide combination as claimed in claim 1 , wherein the weight ratio (A):

(B) of the components (A) and (B) is in the range of from 1:5000 to 500:1.

3. The herbicide combination as claimed in claim 1 , comprising one or more further components selected from the group of agrochemically active compounds formulation auxiliaries and additives customary in crop protection.

4. The herbicide combination as claimed in claim 1 , wherein the weight ratio (A):

(B) of the components (A) and (B) is in the range of from 1:1000 to 250:1.

5. The herbicide combination as claimed in claim 1 , wherein the weight ratio (A):

(B) of the components (A) and (B) is in the range of from 1:160 to 100:1.

6. The herbicide combination as claimed in claim 1 , further comprising a herbicide that is herbicidally active based on inhibition of acetolactate synthase, acetyl coenzyme A carboxylase, cellulose synthase, enolpyruvylshikimate 3-phosphate synthase, glutamine synthetase, p-hydroxyphenylpyruvate dioxygenase, phytoene desaturase, or protoporphyrinogen oxidase.

7. The herbicide combination as claimed in claim 1 , further comprising a safener, wherein the weight ratio of the components (A) and (B): safener is in the range of from 3000:1 to 1:500.

8. A method for controlling a weed, the method comprising separately or jointly applying to one or more of a plant, a seed, or an area under cultivation

(A) a compound of formula (A1) or salt thereof

 and

(B) saflufenacil.

9. The method as claimed in claim 8 wherein said weed is controlled in a crop plant selected from wheat, durum wheat, common wheat, corn, soybeans, sugar beet, sugar cane, cotton, rice, beans, flax, barley, oats, rye, triticale, oilseed rape, potatoes, millet, sorghum, pasture grass, greens/lawns; in a fruit plantation crop; or on a non-crop area.

10. The method as claimed in claim 8 wherein the components (A) and (B) are applied jointly.

11. The method as claimed in claim 8 wherein the components (A) and (B) are applied separately.

12. The method as claimed in claim 8 wherein said weed is controlled in rice.

13. The method as claimed in claim 8 wherein said weed comprises a plant selected from one or more of the group consisting of broad-leaved weeds, weed grasses, and Cyperaceae that are resistant to herbicidally active compounds selected from the group consisting of glyphosate, glufosinate, atrazine, imidazolinone herbicides, sulfonylureas, (hetero)aryloxyaryloxyalkylcarboxylic acids, -phenoxyalkylcarboxylic acids, cyclohexanedione oximes, and auxin inhibitors.

14. The method as claimed in claim 8 , wherein the weight ratio (A) : (B) of the components (A) and (B) is in the range of from 1:1000 to 250:1.

15. The method as claimed in claim 8 , wherein the weight ratio (A) : (B) of the components (A) and (B) is in the range of from 1:160 to 100:1.

16. The method as claimed in claim 8 , wherein component (A) is applied at an application rate 0.1-1000 g of active substance per hectare.

17. The method as claimed in claim 8 , wherein component (A) is applied at an application rate 0.1-500 g of active substance per hectare.

18. The method as claimed in claim 8 , wherein component (B) is applied at an application rate 1-1000 g of active substance per hectare.

19. The method as claimed in claim 8 , wherein component (B) is applied at an application rate 2-800 g of active substance per hectare.

Assignments (5)
NUNC PRO TUNC ASSIGNMENT Recorded Jul 4, 2023
From: BAYER INTELLECTUAL PROPERTY GMBH
To: BAYER CROPSCIENCE AKTIENGESELLSCHAFT
Reel/Frame 064198/0823 →
CHANGE OF ADDRESS Recorded Jun 12, 2023
From: BAYER INTELLECTUAL PROPERTY GMBH
To: BAYER INTELLECTUAL PROPERTY GMBH
Reel/Frame 064021/0344 →
CORRECTIVE ASSIGNMENT TO CORRECT THE ASSIGNEE ADDRESS PREVIOUSLY RECORDED AT REEL: 034891 FRAME: 0140. ASSIGNOR(S) HEREBY CONFIRMS THE ASSIGNMENT. Recorded Feb 19, 2015
From: BAYER CROPSCIENCE AG
To: BAYER INTELLECTUAL PROPERTY GMBH
Reel/Frame 035046/0921 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 3, 2015
From: BAYER CROPSCIENCE AG
To: BAYER INTELLECTUAL PROPERTY GMBH
Reel/Frame 034891/0140 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 3, 2011
From: HACKER, ERWIN, DR.; WALDRAFF, CHRISTIAN, DR.; ROSINGER, CHRISTOPHER HUGH, DR.; UENO, CHIEKO, DR.; BONFIG-PICARD, GEORG, DR.; SCHNATTERER, STEFAN, DR.; SHIRAKURA, SHINICHI
To: BAYER CROPSCIENCE AG
Reel/Frame 026213/0466 →