AU2007200896A1 - Synergistic Herbicidal Methods & Compositions - Google Patents

Description

P001 Section 29 Regulation 3.2(2)

AUSTRALIA

Patents Act 1990 COMPLETE SPECIFICATION STANDARD PATENT Application Number: Lodged: Invention Title: Synergistic Herbicidal Methods Compositions The following statement is a full description of this invention, including the best method of performing it known to us: 0 SYNERGISTIC HERBICIDAL METHODS AND COMPOSITIONS CN This application is a divisional application of Australian application no.

11369/01, the entire contents of which are incorporated herein by cross Sreference.

0 5 Aryloxypicolinamides such as those described in U.S. 5,294,597 demonstrate excellent herbicidal activity, in particular against broadleaf weeds in N cereal crops. However, said aryloxypicolinamides, when used as the sole active o00 0 ingredient, do not always achieve effective control of the full spectrum of weed Sspecies encountered in commercial agronomic practice at application rates required for acceptable crop safety. Such gaps in the spectrum of control can C- often be remedied by co-treatment with another herbicide known to be effective against the relevant weed species. It has been disclosed 5,674,807) that selected combinations of aryloxypicolinamides produce not merely the expected additive effect, but may exhibit a significant synergistic effect the combination shows a much higher level of activity than that which could be predicted from that of the individual components). This synergistic effect enables a greater margin of safety for the crop species. However, the disclosure is limited to two-way combinations of aryloxypicolinamides and members of selected known chemical classes which do not include herbicidal partners in the imidazolinone, cyclohexanedione, aryloxyphenoxypropionic acid, or pyridinecarboxylic acid classes. Moreover, although the phenoxyacetic acid chemical class is disclosed, 2,4-dichlorophenoxyacetic acid its esters and salts are not specifically exemplified.

Therefore it is an object of this invention to provide synergistic, cropselective herbicidal combinations with broad-spectrum weed control.

It is another object of this invention to provide herbicidal compositions useful for the synergistic control of a broad-spectrum of weeds in the presence of a crop.

Although aryloxypicolinamide compounds demonstrate excellent herbicidal activity, when applied alone they do not always achieve the desired spectrum of weed control at rates required for acceptable crop safety. Surprisingly, it has now been found that a two-way combination comprising an aryloxypicolinamide compound of formula I o c R y 0 N(CHR) z O I 00 Swherein c- 0 Z represents an oxygen or sulfur atom; cN R represents a hydrogen or halogen atom or an alkyl or haloalkyl group;

R

2 represents a hydrogen or an alkyl group; q is 0 or 1;

R

3 represents a hydrogen or an alkyl or alkenyl group; the or each group X independently represents a halogen atom or an optionally substituted alkyl or alkoxy group, preferably a haloalkyl group, or an alkenyloxy, cyano, carboxy, alkoxycarbonyl, (alkylthio)carbonyl, alkylcarbonyl, amido, alkylamido, nitro, alkylthio, haloalkylthio, alkenylthio, alkynylthio, alkylsulphinyl, alkylsulphonyl, alkyloxyminoalkyl or alkenyloximinoalkyl group; n is 0 or an integer from 1 to the or each group Y independently represents a halogen atom or an alkyl, nitro, cyano, haloalkyl, alkoxy or haloalkoxy group; and m is 0 or an integer from 1 to or one of its environmentally compatible salts; plus a second herbicide selected from an imidazolinone or a pyridinecarboxylic acid herbicide demonstrates a synergistic herbicidal effect.

Further, unexpectedly, a selected three-way combination comprising an aryloxypicolinamide compound of formula I and 2,4-D or one of its environmentally compatible esters or salts; and a third herbicide consisting of an imidazolinone herbicide produces a significant synergistic effect. Advantageously, the synergistic two-way and three-way combinations of the invention allow for lower application rates of said aryloxypicolinamide with concomittant increased Sspectrum of weed control. Moreover, the synergistic herbicidal methods and

O

C compositions of the invention allow for effective resistance management.

SThe present invention provides a method for the synergistic control of Sundesirable plants such as Polygonum, Kochia, Galeopsis, Galium, Stelaria, Sinapis, and Avena which comprises applying to the locus of said plants or to the foliage or stems of said plants a synergistically effective amount of a two-way ND combination comprising an aryloxypicolinamide compound of formula I plus a oo second herbicide selected from an imidazolinone or a pyridinecarboxylic acid Sherbicide. The present invention also provides a method for the synergistic control of undesirable plants which comprises applying to the locus of said plants a synergistically effective amount of a three-way combination comprising an aryloxypicolinamide compound of formula I, 2,4-D or one of its environmentally compatible esters or salts, and a third herbicide consisting of an imidazolinone herbicide.

The present invention also provides a synergistic herbicidal composition which comprises an agriculturally acceptable carrier and a synergistically effective amount of a two-way combination of an aryloxypicolinamide compound of formula I plus a second herbicide selected from an imidazolinone or a pyridinecarboxylic acid herbicide; or a three-way combination of an aryloxypicolinamide compound of formula I, 2,4-D or one of its environmentally compatible esters or salts, and a third herbicide consisting of an imidazolinone.

Aryloxypicolinamides of formula I

I

wherein Z, Ri, R 2

R

3 X, n, Y and m are defined herein above and methods for their preparation are described in U.S. 5,294,597. Said aryloxypicolinamides demonstrate excellent herbicidal activity, in particular 0 against broadleaf weeds in cereal crops. However, said aryloxypicolinamides

O

c- when used as the sole active ingredient do not always achieve effective control of S the full spectrum of weed species encountered in commercial agronomic practice, Sin conjunction with reliable selectivity for the crop species.

0 5 Surprisingly, it has now been found that a two-way combination of an aryloxypicolinamide of formula I and a second herbicide selected from an N imidazolinone or a pyridinecarboxylic acid herbicide provides synergistic control 00 of troublesome weeds such as Polygonum, Kochia, Galeopsis, Galium, Stelaria, SSinapis, and Avena. Also, surprisingly, a three-way combination of an aryloxypicolinamide of formula I and 2,4-D or one of its environmentally compatible esters or salts plus a third herbicidal compound consisting of an imidazolinone herbicide provides synergistic weed control. That is, the application of the two-way or three-way combinations of the invention gives a mutual reinforcing action such that the application rates of the individual herbicidal components can be reduced and still the same herbicidal effect is achieved or, alternatively, the application of the combination of herbicidal components demonstrates a greater herbicidal effect than expected from the effect of the application of the individual herbicidal components when applied singly at the rate at which they are present in the combination (synergistic effect).

The aryloxypicolinamides of formula I may exist in the form of their environmentally compatible salts. Suitable salts are, in general, the salts of those cations, or the acid addition salts of those acids, whose cations, or anions, respectively, do not adversely affect the herbicidal action of the active ingredients.

Suitable cations are, in particular, ions of the alkali metals, preferably lithium, sodium and potassium, of the alkaline earth metals, preferably calcium and magnesium, and of the transition metals, preferably manganese, copper, zinc and iron, and also ammonium, it being possible in this case, if desired, for one to four hydrogen atoms to be replaced by C1-C 4 -alkyl, hydroxy-C 1

-C

4 -alkyl, C1-C 4 alkoxy-C 1

-C

4 -alkyl, hydroxy-Ci-C 4 -alkoxy-C 1

-C

4 -alkyl, phenyl or benzyl, preferably ammonium, dimethylammonium, diisopropylammonium, tetramethylammonium, tetrabutylammonium, 2-(2-hydroxyeth-1-oxy)eth-1-yl ammonium, di(2-hydroxyeth- 1-yl)ammonium, trimethylbenzylammonium, furthermore phosphonium ions, sulfonium ions, preferably tri(C1-C 4 -alkyl)sulfonium and sulfoxonium ions, N preferably, tri(C1-C 4 -alkyl)sulfoxonium.

Anions of suitable acid addition salts are mainly chloride, bromide, fluoride, hydrogen sulfate, sulfate, dihydrogen phosphate, hydrogen phosphate, nitrate, hydrogen carbonate, carbonate, hexafluorosilicate, hexafluorophosphate, benzoate and the anions of C1-C 4 -alkanoic acids, preferably formate, acetate, ID propionate and butyrate.

00In the specification and claims, the term 2,4-D designates 2,4dichlorophoxyacetic acid. 2,4-0 may also exist in the form of its environmentally compatible esters or salts. Suitable salts are, in general, the salts of those cations, which do not adversely affect the herbicidal action of the active ingredients.

Suitable cations are, in particular, ions of the alkali metals, preferably lithium, sodium and potassium, of the alkaline earth metals, preferably calcium or magnesium, and of the transition metals, preferably manganese, copper, zinc and iron, and also ammonium, it being possible in this case if desired, for one to four hydrogen atoms to be replaced by C 1

-C

4 -alkyl, hydroxy-C1-C 4 -alkyl, C1-C4alkoxy-C 1

-C

4 -alkyl, hydroxy-C 1

-C

4 -alkoxy-C 1 -C4- alkyl, phenyl or benzyl, preferably ammonium, dimethylammonium, diisopropylammonium, (2-hydroxyeth-1-yl)ammonium, di(2-hydroxy-eth-1-yl)ammonium or tri(2-hydroxy-eth-1 yl)ammonium.

Especially suitable cations are sodium, dimethylammonium, di(2-hydroxyeth-1-yl)ammonium and tri(2-hydroxy-eth-1-yl)ammonium.

Suitable esters of 2,4-D are the C 1

-C

8 -alkyl esters, for example the methyl, ethyl, propyl, 1-methylethyl, butyl, 1-methylpropyl, 2-methylpropyl, 1,1dimethylethyl, pentyl, 1-methylbutyl, 2-methylbutyl, 3-methylbutyl, 2,2dimethylpropyl, 1-ethylpropyl, hexyl, 1,1-dimethylpropyl, 1,2-dimethylpropyl, 1methylpentyl, 2-methylpentyl, 3-methylpentyl, 4-methylpentyl, 1,1-dimethylbutyl, 1,2-dimethylbutyl, 1,3-dimethylbutyl, 2,2-dimethylbutyl, 2,3-dimethylbutyl, 3,3dimethylbutyl, 1-ethylbutyl, 2-ethylbutyl, 1,1 ,2-trimethylpropyl, 1-ethyl-1methylpropyl, 1-ethyl-3-methylpropyl, heptyl, 5-methyl-l-hexyl, octyl, 6-methyl- 1-heptyl, 2-ethyl-1-hexyl or 4-ethyl-1-hexyl esters, or the Cl-C 4 -alkoxy-C 1

C

4 -alkyl esters for example the methoxymethyl, ethoxymethyl, propoxymethyl, (1 -m ethyl ethoxy) methyl, butoxymethyl, (1 -methylpropoxy)methyl, (2- N- methyl pro poxy)-methyl, 1 -d i methyl ethoxy)mrnethyl, 2-(methoxy)ethyl, 2- (ethoxy)ethyl, 2-(propoxy)ethyl, 2-(lI-methylethoxy)ethyl, butoxy)ethyl, 1methylpropoxy)ethyl, 2-(2-methylpropoxy) ethyl, 2-(1I, 1 -d imnethyl ethoxy)ethyl, 2- C) 5 (methoxy)propyl, 2-(ethoxy)propyl, 2-<propoxy)propyl, 2-(l1-methylethoxy)propyl, 2-(butoxy)propyl, 1 -methyl pro poxy)p ropyl, -2 INDmethylpropoxy)propyl, 1,1 -d imethylethoxy)propyl, 3-(methoxy)propyl, 3- 00\ 00 (ethoxy)-propyl, 3-(propoxy)propyl, 3-(l1-methylethoxy)propyl, 3-(butoxy)propyl, 1 -methylpropoxy)propyl, 3-(2-m ethyl pro poxy)p ro pyl, 1,1 d imethylethoxy)propyl, 2-(methoxy)butyl, 2-(ethoxy)butyl, 2-(propoxy)butyl, 2- (1 -methylethoxy)butyl, 2-(butoxy)butyl, 1 -methylpropoxy)butyl, 21(2methylpropoxy)butyl, 1,1 -d imethylethoxy)butyl, methoxy)butyl, 3-(ethoxy)butyl, 3-(propoxy)butyl, 3-(methylethoxy)butyl, 3-(butoxy)butyl), 1methylpropoxy)butyl, 3-(2-methylpropoxy)butyl, 1,1 -dimethylethoxy)butyl, 4- (methoxy)butyl, 4-(ethoxy)butyl, 4-(propoxy)butyl, 4-(1 -methylethoxy)butyl, 4- (butoxy)butyl, 4-(l1-methylpropoxy)butyl, 4-(2-methyl pro poxy)butyl or 1,1,dimethylethoxy)butyl esters.

Especially suitable esters are the 1 -methyl-i -ethyl, butyl, 6-methyl-Iheptyl, 2-ethyl-I -hexyl or 2-butoxy-1 -ethyl esters.

Examples of an imidazolinone herbicide suitable for use in the methods and compositions of the invention include imazapyr, imazethapyr, imazapic, imazaquin, imazamox, imazamethabenz methyl, imazamethapyr or the like or one of its environmetntally compatible salts, preferably imazamethabenz methyl.

Suitable salts are in general, the salts of those anions which do not adversely affect the herbicidal action of the active ingredient. They are similar to those listed for the compounds of formula I.

A pyridinecarboxylic acid herbicide such as picloran, clopyralid, or the like, preferably clopyralid, is suitable for use in the two-way combination of the invention. Also salts thereof may be used. Suitable salts are similar to those listed for 2,4-D.

In the specification and claims, the term alkyl (alone or in combination) represents a 0 1 -0 6 -alkyl group, especially a 0 1 -0 4 -alkyl group; the term alkoxy (alone or in combination) represents a Cl-C 6 -alkoxy group, especially a Cl-C 4 0 alkoxy group; the term alkenyl (alone or in combiantion) represents a C 3

-C

6

O

CN alkenyl group, especially a C 3

-C

4 -alkenyl group; the term alkynyl represents a S C 3

-C

6 -alkynyl group, especially a C 3

-C

4 -alkynyl group.

SPreferred synergistic combinations of the invention are those two-way or 0 5 three-way combinations containing a formula I aryloxypicolinamide wherein Z is oxygen;

SR

1 is hydrogen; 00 0 qis 0; p R 3 is hydrogen; 0 10 X is haloalkyl; and c Y is hydrogen or fluorine.

Especially those two-way or three-way combinations containing a formula I aryloxypicolinamide wherein n=1 and X is linked in meta-position to the phenyl radical (with regard to the oxygen bridge).

More preferred synergistic two-way and three-way combinations are those wherein the formula I compound is N-(4-fluorophenyl)-6-[3trifluoromethyl)phenoxy]-2-pyridine carboxamide ilustrated below, and hereinafter designated, picolinafen.

CFH

0 picolinafen Preferred second herbicides for the two-way combinations of the invention are 2,4-D, imazamethabenz methyl, fenoxaprop-p-ethyl, and clopyralid.

Another preferred embodiment of the invention are those two-way combinations wherein the second herbicide is 2,4-D or one of its environmentally compatible esters or salt, expecially 2,4-D.

Another preferred embodiment of the invention are those two-way combinations wherein the second herbicide is selected from the group consisting of an imidazolinone herbicide and a pyridinecarboxylic acid herbicide. Especially the second herbicide is imazamethabenz methyl or clopyralid.

SAnother preferred embodiment of the invention are those two-way

O

C combinations wherein the second herbicide is an aryoxyphenoxy-propionate Sherbicide. Especially the second herbicide is fenoxaprop-p-ethyl.

SPreferred third herbicides for the three-way combination of the invention are imazamethabenz methyl or fenoxaprop-p-ethyl.

Another preferred embodiment of the invention are those three-way I combinations wheren the third herbicide is an imidazolinone herbicide.

0O Especially the third herbicide is imazamethabenz methyl.

SAnother preferred embodiment of the invention are those three-way combinatins wherein the third herbicide is an ayloxyphenoxypro-pionate Sherbicide. Especially the second herbicide is fenoxaprop-p-ethyl.

In actual practice, the combination of the invention may be applied simultaneously (as a tank mix or a premix), separately or sequentially.

Thus, in accordance with the method of invention a synergistically effective amount of a two-way combination of aryloxypicolinamide and a second herbicide selected from 2,4-D, or one of its environmentally compatible salts or esters, an imidazolinone, or a pyridinecarboxylic acid herbicide; or a synergistically effective amount of a three-way combination of an aryloxypicolinamide, 2,4-D, or one of its environmentally compatible salts or esters and a third herbicidem, an imidazolinone is applied to the locus, foliage or stems of undesirable plants, particularly plants selected from the genera Polygonum, Kochia, Galeopsis, Galium, Stelaria, Sinapis, and Avena, optionally in the presence of a crop, preferably a cereal crop such as wheat, barley, rice, corn, rye or the like.

The synergistically effective amount of the two- and three-way combinations described above may vary according to prevailing conditions such as the particular second and third component present, weed pressure, application timing, weather conditions, soil conditions, mode of application, topographical character, target crop species and the like.

Preferred two-way combinations of the invention are those wherein the weight/weight ratio of the aryloxypicolinamide of formula I to the second compound is about: aryloxypicolinamide:2,4 D (or its salts or ester), 1:1 to 1:25; aryloxypicolinamide:imidazolinone herbicide, 1:1 to 1:35; Saryloxypicolinamide:aryloxyphenoxypropionate herbicide, 1:1 to 1:10;

O

CN aryloxpicalinamide:pyridicarboxylic acid herbicide, 1:1 to 1:15.

More preferred two-way combinations of the invention are those wherein Sthe weight/weight ratio of picolinafen to the second component is about: 0 5 picolinafen:2,4-D, 1:1 to 1:25; picolinafen:imazethabenz methyl, 1:1 to 1:35; N picolinafen:fenoxaprop-p-ethyl, 1:1 to 1:10; or O picolinafen:clopyralid, 1:1 to 1:15.

SPreferred three-way combinations of the invention are those wherein the weight/weight ratio of the aryloxypicolinamide of formula I to 2,4-D (or its salts or esters) to third component is about: aryloxypicolinamide: 2,4 D (or its salts or esters): imidazolinone herbicide, 1:1:1 to 1:35:25; aryloxypicolinamide: 2,4 D (or its salts or esters): aryloxyphenoxypropionate herbicide, 1:1:1 to 1:10:25.

More preferred three-way combinations of the invention are those wherein the weight/weight/weight ratio of picolinafen to 2,4-D to third component is about: picolinafen: 2,4-D:imazamethabenz methyl, 1:1:1 to 1:35:25; or picolinafen: 2,4-D:fenoxaprop-p-ethyl, 1:1:1 to 1:10:25.

The present invention also provides a synergistic herbicidal composition comprising an agriculturally acceptable carrier and a synergistically effective amount of a two-way combination of an aryloxypicolinamide of formula I and a second herbicidal compound selected from the group consisting of an imidazolinone herbicide and a pyridinecarboxylic acid herbicide. The present invention further provides a synergistic herbicidal composition which comprises an agriculturally acceptable carrier and a synergistically effective amount of a three-way combination of an aryloxypicolinamide compound of formula I, 2,4-D, or one of its environmentally compatible salts or esters and a third herbicidal compound consisting of an imidazolinone herbicide.

The agriculturally acceptable carrier may be a solid or a liquid, preferably a liquid, more preferably water. While not required, the combination compositions of the invention may also contain other additives such as fertilizers, inert formulation aids, i.e. surfactants, emulsifiers, defoamers, dyes, extenders or any 0 of the conventional inert ingredients typically employed in herbicidal formulated

O

products.

Compositions according to the invention may be formulated in any Sconventional form, for example in the form of a twin pack, or as an aqueous concentrate, soluble granular, dispersible granular or the like.

Preferred two-way combination compositions of the invention are those compositions wherein the aryloxypicolinamide compound is picolinafen. Also 0 preferred are those synergistic two-way combination compositions having a second herbicide selected from the group consisting of 2,4-D, imazamethabenz methyl, fenoxaprop-p-ethyl and clopyralid. More preferred two-way combination compositions of the invention are those compositions of the invention wherein the weight/weight ratio of picolinafen to second component is about: picolinafen: 2,4-D, 1:1 to 1:25; picolinafen: imazethabenz methyl, 1:1 to 1:35; picolinafen:fenoxaprop-p-ethyl, 1:1 to 1:10; or picolinafen:clopyralid, 1:1 to 1:15.

Preferred three-way combination compositions of the invention are those compositions wherein the picolinamide compound is picolinafen. Also preferred are those synergistic three-way combination compositions having a third herbicide selected from the group consisting of imazamethabenz methyl and fenoxaprop-p-ethyl. More preferred three-way combination compositions of the invention are those compositions wherein the weight/weight/weight ratio of picolinafen to 2,4-D to third component is about: picolinafen: 2,4-D:imazamethabenz methyl, 1:1:1 to 1:35:25; or picolinafen: 2,4-D:fenoxaprop-p-ethyl, 1:1:1 to 1:10:25.

For a more clear understanding of the invention, specific examples thereof are set forth below. These examples are merely illustrative, and are not to be understood as limiting the scope and underlying principles of the invention in any way.

In the following examples, synergism for two-way combinations is determined by the Colby method Colby, Weeds 1967 20), i.e. the expected (or predicted) response of the combination is calculated by taking the product of the observed response for each individual component of the Scombination when applied alone divided by 100 and subtracting this value from C the sum of the observed response for each component when applied alone.

t Synergism of the combination is then determined by comparing the observed Sresponse of the combination to the expected (or predicted) response as calculated from the observed responses of each individual component alone. If the observed response of the combination is greater than the expected (or INDpredicted) response then the combination is said to be synergistic and falls within 00 the definition of synergistic effect as previously defined.

SThe foregoing is illustrated mathematically below, wherein a two-way combination, C2, is composed of component X plus component Y and Obs.

Sdesignates the observed response of the combination 02.

XY

(X Y) Expected response (Exp.) 100 SynergismE-- Obs. Exp.

In similar manner for the case of three-way combination, C3, is composed of component X plus component Y plus component X and Obs. designates the observed response of the combination C3.

(XY+XZ+YZ) XYZ (X Y Exp.

100 10000 Synergism Obs. Exp.

In the following examples, crop tolerance ratings are taken periodically throughout the growing season. The first rating is taken one to two weeks after treatment and the final rating is taken just prior to harvest. For all treatments described in the following examples crop tolerance was commercially acceptable, i.e. 20% injury, on each of the three crops tested. None of the treatments demonstrated commercially unacceptable injury to barley, durum wheat or hard red spring wheat.

L EXAMPLE 1 N Evaluation of the Herbicidal Activity of a Combination of Picolinafen and 2,4-Dichlorophenoxyacetic Acid SGrassy and broadleaved weeds are either seeded perpendicular to the direction of the crop or broadcast in early to mid-May. The crop is seeded after the weed seed. Row width is 18 cm. The seed is drilled in with a Roger's 1.8 m I width drill to a depth of 5 cm.

0O All trials employ standard accepted weed science procedures. Applications Sare made with a Roger's CO2-powered shrouded sprayer. Test design is a modified randomized complete block design with four replications. All applications S are made post-emergence to the weeds and crop.

The test solutions are prepared by tank-mixing sufficient quantities of aqueous solutions and/or dispersions of the test compounds.

The treated plots are examined at intervals during the growing season and rated for percent control of weeds and crop injury. The data listed is an average of the replicates for that treatment. The Colby method of analysis is used to determine the resultant biological effect of the combination treatment as compared to the biological effect of each component when applied alone. The data are reported in Table I.

As can be seen from the data shown in Table I, application of a combination of picolinafen plus 2,4-D gave significantly greater weed control than that which could be predicted from the weed control resulting from the application of either picolinafen alone or 2,4-D alone.

TABLE I Evaluation of the Herbicidal Activity of a Combination of Picolinafen plus 2,4-D picolinafen 2,4-D picolinafen 2,4-D 280g/ha 50g/ha 280 g/ha Weed Species PERCENT CONTROL OBSERVED EXPECTED Avena fatua 5 2 15 7 Chenopodium album 57 91 97 96 Polygonum convolvulus 54 48 80 76 Galeopsis tetrahit 59 2 70 Polygonum (smartweed) 26 53 85 spp.

S| Vaccaria pyramaidata I 63 1 51 I 97 I 82 EXAMPLE 2 SEvaluation of the Herbicidal Activity of a Combination of Picolinafen and Imazamethabenz Methyl Following essentially the same procedure described in Example 1 and IN employing picolinafen and imazamethabenz methyl, the data shown in Table II oo are obtained.

0As can be seen from the data in Table II, the application of a combination of picolinafen plus imazamethabenz methyl gives significantly greater weed 0 10 control than that which could be predicted from the weed control resulting from the application of either picolinafen alone or imazamethabenz methyl alone.

the application of either picolinafen alone or imazamethabenz methyl alone.

2007200896 01 Mar 2007 TABLE II Evaluation of the Herbicidal Activity of a Combination of Picolinafen plus Imazamethabenz Methyl Weed Species picolinafen imazaniethabenz picolinaffen methyl imazamethabenz methyl 4 0g/ha 50g/ha 400 g/ha PERCENT CONTROL OBSERVED EXPECTED Avena fatua 5 88 91 89 Setaria viridis 14 10 42 23 Brassica napus (Imidazolinone 65 0 86 tolerant) Chenopodium album 57 18 86 Galeopsis tetrahit 59 4 76 61 Galium aparine 28 48 90 63 Polygonum spp. 26 76 84 82 Kochia scoparia 59 31 85 72 Salsola kali 56 9 79 Vaccania pyramaidata 63 20 77 SEXAMPLE 3 0 cEvaluation of the Herbicidal Activity of a Combination of Picolinafen and Fenoxaprop-p-ethyl SFollowing essentially the same procedure as described in Example 1 and employing picolinafen and fenoxaprop-p-ethyl, the data shown in Table IV are obtained.

N As can be seen from the data shown on Table IV, the application of a combination of picolinafen plus fenoxaprop-p-ethyl gives significantly greater Sweed control than that which could be predicted from the weed control resulting from the application of either picolinafen alone or fenoxaprop-p-ethyl alone.

2007200896 01 Mar 2007 TABLE III Evaluation of the Herbicidal Activity of a Combination of Picolinafen plus Fenoxaprop-p-ethyl picolinafen fenoxaprop-p-ethyl picolinafen fenoxaprop-p-ethyl 72g/ha 50g/ha 72 g/ha Weed Species PERCENT CONTROL OBSERVED EXPECTED Sinapis arvensis 78 0 96 78 Setaria viridis 14 98 99 98 Brassica napus 70 0 97 Brassica napus (imidazolinone 65 0 97 tolerant) Ainaranthus retroflexus 90 9 94 91 Chenopodiun album 57 0 95 57 Polygonun convolvulus 54 0 74 54 Vaccaria pyrainaidata 63 0 71 63 0 EXAMPLE 4 C Evaluation of the Herbicidal Activity of a Combination of Picolinafen and SClopyralid Following essentially the same procedure as in Example 1 and employing 0 5 picolinafen and clopyralid, the data shown in Table V are obtained.

As can be seen from the data shown on Table IV the application of a Scombination of picolinafen plus clopyralid gives significantly greater weed control 00 Sthan that which could be predicted from the weed control resulting from the Sapplication of either picolinafen alone or clopyralid alone.

2007200896 01 Mar 2007 TABLE IV Evaluation of the Herbicidal Activity of a Combination of Picolinafen plus Clopyralid picolinafen clopyralid picolinafen clopyralid I150g/ha 50g/ha 150g/ha Weed Species PERCENT CONTROL OBSERVED EXPECTED Sinapis arvensis 78 16 87 82 Brassica napus 70 12 78 74 Brassica napus 65 8 85 68 (imidazolinone tolerant) Chenopodium album 57 51 83 79 Stellaria media 64 10 70 68 Galium aparine 28 0 30 28 0 EXAMPLE 0 N Evaluation of the Herbicidal Activity of a Combination of Picolinafen, S Imazamethabenz Methyl and 2,4-D Following essentially the same procedure as described in Example 1 and employing picolinafen, 2,4-D and imazamethabenz methyl, the data shown in Table VI are obtained.

N As can be seen from the data on Table VI, the application of a combination 0 of picolinafen, 2,4-D and imazamethabenz methyl gives significantly greater weed 0 control than that which could be predicted from the weed control resulting from the application of picolinafen alone, 2,4-D alone or imazamethabenz methyl 0 alone.

2007200896 01 Mar 2007 TABLE V Evaluation of the Herbicidal Activity of a Combination of Picolinafen, 2,4-D and Imazamnethabenz Methyl picolinafei imazamethabenz methyl 2,.4-D picolinafen 2,4-D 400 g/ha 280g/ha imazamethabenz methyl 280 /ha 400g/ha Weed Species Percent Control Observed Expected Avena fatua 5 88 2 91 89 Setaria viridis 14 10 0 49 23 Stellaria media 64 8 10 86 Galeopsis tetrahit 59 4 2 82 61 Galium aparine 28 48 43 94 79 Polygonum spp. 26 76 53 99 92 Kochia scoparia 59 31 52 93 86 Salsola kali 56 9 35 97 74 Vaccaria pyramaidata 63 20 51 93 0 EXAMPLE 6 CN Evaluation of the Herbicidal Activity of a Combination of Picolinafen, 2,4-D Sand Fenoxaprop-p-ethyl SFollowing essentially the same procedure as described in Example 1 and employing picolinafen, 2,4-D and fenoxaprop-p-ethyl, the data shown in Table VIII are obtained.

N As can be seen from the data shown in Table VIII, the application of a 0 combination of picolinafen, 2,4-D and fenoxaprop-p-ethyl gives significantly greater weed control than that which could be predicted from the weed control O 10 resulting from the application of picolinafen alone, or 2,4-D alone or fenoxaprop- C- p-ethyl alone.

2007200896 01 Mar 2007 TABLE TABLE VI Evaluation of the Herbicidal Activity of a Combination of Picolinafen, plus 2,4-D and Fenoxaprop-p-ethyl picolinafen fenoxaprop-p- 2, 4-D picolinafen 2,4-D fenoxaprop-pethyl j280g/ha ethyl 72 g/ha 50g/ha 280g/ a 72g/ha PERCENT CONTROL OBSERVED EXPECTED Weed Species Brassica napus 70 0 93 100 98 Brassica napus 65 0 94 100 98 (imidazolinone tolerant) Chenopodium. album 57 0 91 97 96 Polygonum convolvulus 54 0 48 93 76 Vaccaria pyramaidata 63 0 51 96 82 SComprises/comprising and grammatical variations thereof when used in Sthis specification are to be taken to specify the presence of stated features, Sintegers, steps or components or groups thereof, but do not preclude the Spresence or addition of one or more other features, integers, steps, components or groups thereof.

00 0"-

Claims (9)

1. A synergistic herbicidal composition which comprises an agriculturally Sacceptable carrier and a synergistically effective amount of a two-way Scombination of an aryloxypicolinamide of formula I R o00r R3 z C I wherein Z represents an oxygen or sulfur atom; R 1 represents a hydrogen or halogen atom or an alkyl or haloalkyl group; R 2 represents a hydrogen or an alkyl group; q is 0 or 1; R 3 represents a hydrogen or an alkyl or alkenyl group; the or each group X independently represents a halogen atom or an optionally substituted alkyl or alkoxy group, preferably a haloalkyl group, or an alkenyloxy, cyano, carboxy, alkoxycarbonyl, (alkylthio)carbonyl, alkylcarbonyl, amido, alkylamido, nitro, alkylthio, haloalkylthio, alkenylthio, alkynylthio, alkylsulphinyl, alkylsulphonyl, alkyloxyminoalkyl or alkenyloximinoalkyl group; n is 0 or an integer from 1 to the or each group Y independently represents a halogen atom or an alkyl, nitro, cyano, haloalkyl, alkoxy or haloalkoxy group; and m is 0 or an integer from 1 to or one of its environmentally compatible salts; and a second herbicide selected from the group consisting of an imidazolinone herbicide and a pyridinecarboxylic acid herbicide. 0 2. The composition according to claim 1 having a formula I c- aryloxypicolinamide wherein Z is oxygen; R 1 is hydrogen; q is 0; R 3 is hydrogen; I X is haloalkyl; and 0 Y is hydrogen or fluorine. (N

3. The composition according to claim 2 wherein said formula I aryloxypicolinamide is picolinafen.

4. The composition according claim 1 wherein the second herbicide is selected from the group consisting of an imidazolinone herbicide and a pyridinecarboxylic acid herbicide. The composition according claim 4 wherein the second herbicide is imazamethabenz methyl or clopyralid.

6. The composition according to any one of claims 4 to 5 wherein said formula I aryloxypicolinamide is picolinafen.

7. A synergistic herbicidal composition which comprises an agriculturally acceptable carrier and a synergistically effective amount of a three-way combination comprising: an aryloxypicolinamide of formula I R 1 N Y ^(CHR 2 q- I wherein Z represents an oxygen or sulfur atom; 0 R 1 represents a hydrogen or halogen atom or an alkyl or haloalkyl CN group; R 2 represents a hydrogen or an alkyl group; Sq is 0 or 1; R 3 represents a hydrogen or an alkyl or alkenyl group; the or each group X independently represents a halogen atom or an N optionally substituted alkyl or alkoxy group, preferably a haloalkyl group, or an 0 alkenyloxy, cyano, carboxy, alkoxycarbonyl, (alkylthio)carbonyl, alkylcarbonyl, amido, alkylamido, nitro, alkylthio, haloalkylthio, alkenylthio, alkynylthio, alkylsulphinyl, alkylsulphonyl, alkyloxyiminoalkyl or alkenyloximinoalkyl group; c n is 0 or an integer from 1 to the or each group Y independently represents a halogen atom or an alkyl, nitro, cyano, haloalkyl, alkoxy or haloalkoxy group; and m is 0 or an integer from 1 to or one of its environmentally compatible salts; 2,4-D or one its environmentally compatible esters or salts and a third herbicide consisting of an imidazolinone herbicide.

8. The composition according to claim 7 having a formula I aryloxypicolinamide wherein Z is oxygen; R 1 is hydrogen; q is R 3 is hydrogen; X is haloalkyl; and Y is hydrogen or fluorine.

9. The composition according to claim 8 wherein said formula I aryloxypicolinamide is picolinafen. The composition according to claim 7 wherein the third herbicide is a imidazolinone herbicide. S11. The composition according to claim 10 wherein the third herbicide is O c imazamethabenz methyl.

12. The composition according to any one of claims 10 to 11 wherein said formula I aryloxypicolinamide is picolinafen. s 5 13. A method for the synergistic control of undesirable plants, which comprises 0o applying to the locus of said plants or to the foliage or stems of said plants a Ssynergistically effective amount of the compositions as claimed in any one of claims 1 to 12.

14. A synergistic herbicidal composition substantially as hereinbefore described with reference to the examples and accompanying tables. BASF AKTIENGESELLSCHAFT WATERMARK PATENT TRADE MARK ATTORNEYS