GB2094146A - Herbicidal compositions containing N-(phosphonomethyl)-glycine - Google Patents
Herbicidal compositions containing N-(phosphonomethyl)-glycine Download PDFInfo
- Publication number
- GB2094146A GB2094146A GB8106611A GB8106611A GB2094146A GB 2094146 A GB2094146 A GB 2094146A GB 8106611 A GB8106611 A GB 8106611A GB 8106611 A GB8106611 A GB 8106611A GB 2094146 A GB2094146 A GB 2094146A
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- United Kingdom
- Prior art keywords
- glycine
- phosphonomethyl
- salt
- acid
- compositions
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
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- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N57/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds
- A01N57/18—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-carbon bonds
- A01N57/20—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-carbon bonds containing acyclic or cycloaliphatic radicals
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- Life Sciences & Earth Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Abstract
This invention relates to herbicidal compositions containing N- (phosphonomethyl)-glycine or a non- phytotoxic salt thereof, in combination with 2,4-dichlorophenoxyacetic acid or alpha -naphthlacetic acid or non-phytotoxic salt of these compounds. By using the compositions according to the invention the herbicidally effective amount of N-(phosphonomethyl)- glycine can considerably be reduced in comparison with the commercially available compositions which contain N-(phosphonomethyl)-glycine as an only active ingredient.
Description
SPECIFICATION
Herbicidal compositions containing N-(phosphonomethyl)-glycine
The invention relates to herbicidal compositions containing N-(phosphonomethy}-glycine or a nonphytotoxic salt thereof, in combination with 2,4-dichlorophenoxyacetic acid or ct-naphthylacetic acid or a non-phytotoxic salt of these compounds.
It is well known from the literature that N-(phosphonomethy)-glycine can successfully be used for combatting weeds, especially perennial, deeply rooted weeds, but is effective also as a total plant killer /United States Patent Specification No. 3,799,758/.
2,4-Dichlorophenoxyacetic acid and a-naphthlacetic acid are also known in the art.
It is the object of the present invention to provide combinations, in which, as a result of using further additives, the herbicidally effective amount of N-(phosphonomethyl)-glycine can considerably be reduced in comparison with the herbicidally effective amount of N-(phosphonomethyl)-glycine in compositions, which contain this compound alone.
The present invention relates to herbicidal compositions comprising a combination of N-(phosphonomethyl)-glycine and 2,4-dichlorophonoxyacetic acid or a-naphthlyacetic acid or a non-phytotoxic salt of these compounds, in an effective amount.
The present invention is based on the recognition that the herbicidally effective amount of N-(phosphonomethyl)-glycine or a salt thereof can considerably be reduced by using it in combination with 2,4-dichlorophenoxyacetic acid or a non-phytotoxic salt of these compounds.
Non-phytotoxic salts of N-(phosphonomethyl)-glycine preferably include alkyl amine salts, preferably having from 1 to 4 carbon atoms.
The preferred salts of 2,4-dichlorophenoxyacetic acid also include alkyl amine salts, preferably having from 1 to 4 carbon atoms, e.g. isopropyl amine, dimethyl amine salts, etc., but other salts, e.g. alkali metal, alkali earth metal salts can also be used.
The herbicidal compositions containing N-(phosphonomethyl)-glycine as active ingredient are commercially available generally as emulsifiable concentrates containing 30 to 36 % by weight of active ingredient.
They are generally employed at a rate of 10 lit./ha.
The compositions according to the invention contain from 0.01 to 95 % by weight of the herbicidally active combination and 5 to 99.9 % by weight of one or more formulation acids.
The total active ingredient concentration preferably is between 0.1 to 85 % by weight, more preferably between 1 to 40 % weight.
The proportion of N-(phosphonomethyl)-glycine to 2,4-dichlorophenoxyacetic acid or a-naphthlacetic acid can be varied within a wide range. The weight ratio of N-(phosphonomethyl)-glycine or a salt thereof to dichlorophenoxyacetic acid or a salt thereof preferably is between 5:1 and 1:5, more preferably between 4:1 and 1:2.
The proportion of N-(phosophonomethyl)-glycine or a salt thereof to -napthylacetic acid or a salt thereof preferably is between 2:1 and 5:1.
Is has surprisingly been found that of the herbicidal compositions according to the invention a smaller amount is required to obtain the same herbicidal effect than of the commercially available compositions, which contain N-(phosphonomethyl)-glycine as a sole active ingredient. In this way N-(phosphonomethyl)glycine can partly be replaced by other agricultural chemicals and its effectivity can be increased.
The formulation aids usuable in the compositions according to the invention are additives generally applied in the preparation of herbicides and described in detail in numerous textbooks. The formulation aids may for example be inert solid or liquid carriers, diluents, surfactants, e.g. dispersing and emulsifying agents, wetting agents, adhesives, etc.
As diluents for example various hydrocarbon derivatives, mineral oil fractions, vegetable and animal oils, polar solvents, water, etc. can be used. By using these formulation aids the compositions may conveniently be formulated as solutions, emulsions and dispersions.
The compositions according to the invention may also be formulated as concentrates, which can be diluted in the place of application with water or any other suitable solvent. Such concentrates include for example pastes, oily dispersions, emulsifiable concentrates, etc.
Suitable surfactants include salts of ligninsulfonic acid, alkylaryl sulfonates, alkyl sulfates, fatty alcohol sulfates, alkylarlypolyglycol ethers. etc.
The present invention and the best modes of carrying out the invention are illustrated in detail by the following Examples which do not however serve to limit the scope of protection sought.
EXAMPLE 1
Field trial
Test plants: Agropyron repens,
Cynodon dactylon and
Sorghum halepense
(perennial, monocotyledonous weeds) Test compounds:
A N-(phosphonomethyl)-glycine
E 2,4-dichlorophenoxyacetic acid dimethyl amine salt
F a-naphthylacetic acid.
Field trials were carried out with the following compositions:
A dispersion of 1.8 and 3.6 kg of compound A in 500 lit. of water is applied to one hectare.
In another test a dispersion of 1.8 kg of a compound A and 0.9 kg of a compound E or F in 500 lit. of water was applied to one hectare.
Control experiments were carried out also with compositions containing 0.9 kg of compound E and F, respectively.
Evaluation was made 30 days after treatment.
The results obtained are given in the following Table 1.
TABLE 1
Plant Active ingredient (kg/ha.)
A E F A+E A+F
1.8 3.6 0.9 0.9 1.8+0.9 1.8+0.9
Agropyron
repens 65 100 0 0 100 100
Cynodon
dactylon 60 95-100 0 0 100 100
Sorghum
halopense 65 100 0 0 100 100 0 = no damage 100 = total killing.
From the data given above it can be seen that the compositions containing a combination of compounds A and E, and A and F, respectively, have the same effect as the compositions containing N-(phosphonomethyl)glycine (compound A) alone, in an amount of 3.6 kg. In other words, when using the combination according to the invention the amount of N-(phosphonomethyl)-glycine required to achieve the same herbicidal effect is reduced by 50 %.
EXAMPLE 2
Field trials
Test plants: Agropyron repens,
Ciochorium intybus,
Plantago media,
Cynodon dactylon,
Achilles distans,
Artemisia vulgaris,
Sochus oleraceus.
Test compounds:
A N-(phosphonomethyl)-glycine
E 2,4-dichlorophenoxyacetic acid dimethyl amine salt.
Field trials were carried out with the following compositions:
A dispersion of 1.08 kg. of compound A and compound E, respectively in 500 lit. of water; and a dispersion of a combination of 0.6 kg. of compound A and 0.2 kg. of compound E in 500 lit. of water.
45 days after spraying it was established that the composition containing a combination of the compounds
A and E had the same herbicidal effect on all test plants as the composition containing N-(phosphonomethyl)glycine alone, i.e. necessary amount of N-(phosphonomethyl)-glycine can be reduced to about 60 %.
Analogeous tests were carried out also Agropyron repens, Achilles distans, Artemisia vulgaris, Cynodon dactylon, Plantago media and Sonchus oleraceus. If was found that a dispersion of 1.8 kg. of
N-(phosphonomethyl)-glycine in 500 lit. of water resulted in killing of 70 % of the weeds 30 days after treatment, while when adding also 10, 20 and 40 % by weight, respectively of 2,4-dichlorophenoxyacetic acid to the compositions, the weed-killing was about 85 to 95 %.
EXAMPLE 3
Emulsifiable concentrates
Ingredients Amount
(parts by weight)
1:1 mixture of N-(phosphonomethyl)
-glycine and 2,4-dichlorophenoxy
acetic acid dimethyl amine salt 10
Isooctylphenol polyglycol ether 10
Water 80
The mixture obtained by mixing the ingredients, optionally immediately before application, is diluted with water to the desired concentration.
EXAMPLE 4
Aqueous dispersion
Ingredients Amount
(parts by weight)
2:1 mixture of N-(phosphono
methyl)-glycine and 2,4-di
chlorophenoxyacetic acid di
methyl amine salt 30
Xylene 80
Ethyleneoxide-oil acid N-monoethanol
amide addition product 10
Dodecylbenzenesulfonic acid Ca 5
Ethyleneoxide-castor oil addition
product 5
This dispersion obtained by admixing the ingredients is diluted with 100 000 parts by weight of water.
EXAMPLE 5
Tank mixture
Ingredients Amount
(parts by weight)
1:2 mixture of N-(phosphonmethyl)
-glycine and 2,4-dichlorophenonxy
acetic acid dimethyl amine salt 10
2,4-dichlorophenoxyacetic acid
dimethyl amine salt 10
ligninesulfonicacid Na 10
The mixture obtained by admixing the ingredients is diluted with 10 000 parts by weight of water The tank mixture contains 0.1 % weight of active ingredient.
Claims (9)
1. Herbicidal compositions comprising a combination of N-(phosphonomethyl)-glycine and 2,4dichlorophenoxyacetic acid or a-naphthylacetic acid or a non-phytotoxic salt of these compounds, in an effective amount.
2. Compositions as claimed in claim 1 containing a combination of N-(phosphonomethyl)-glycine and 2,4-dichlorphenoxyacetic acid or a salt of these compounds.
3. Compositions as claimed in claim 2 wherein the weight ratio of N-(phosphomethyl)-glcyine or a salt thereof to 2,4-dichlorophenoxyacetic acid or a salt thereof is between 5:1 and 1:5.
4. Compositions as claimed in claim 3 wherein the weight ratio of N-(phsophonomethyl)-glycine or a salt thereof to 2,4-dichlorphenoxyacetic acid or a salt thereof is between 4:1 and 1:2.
5. Compositions as claimed in claim 1 containing a combination of N-(phosphonomethyl)-glycine and a-naphthylacetic acid or a salt of these compounds.
6. Compositions as claimed in claim 5 wherein the weight ratio of N-(phsophonomethyl)-glycine or a salt thereof to a-naphthylacetic acid or a salt thereof is between 2:1 and 5:1.
7. Compositions as claimed in any one of claims 1 to 6 containing from 0.01 to 95 % by weight of one or more formulation aids.
8. A composition as claimed in claim 1 substantially as described herein in any one of the Examples.
9. The use of a composition as claimed in any one of the preceding claims as a herbicide.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB8106611A GB2094146B (en) | 1981-03-03 | 1981-03-03 | Herbicidal compositions containing n-(phosphonomethyl)-glycine |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB8106611A GB2094146B (en) | 1981-03-03 | 1981-03-03 | Herbicidal compositions containing n-(phosphonomethyl)-glycine |
Publications (2)
Publication Number | Publication Date |
---|---|
GB2094146A true GB2094146A (en) | 1982-09-15 |
GB2094146B GB2094146B (en) | 1984-07-18 |
Family
ID=10520092
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB8106611A Expired GB2094146B (en) | 1981-03-03 | 1981-03-03 | Herbicidal compositions containing n-(phosphonomethyl)-glycine |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB2094146B (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1989004607A1 (en) * | 1987-11-18 | 1989-06-01 | MTA Növényvédelmi Kutatóintézete | Herbicide composition containing at least two active agents |
-
1981
- 1981-03-03 GB GB8106611A patent/GB2094146B/en not_active Expired
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1989004607A1 (en) * | 1987-11-18 | 1989-06-01 | MTA Növényvédelmi Kutatóintézete | Herbicide composition containing at least two active agents |
Also Published As
Publication number | Publication date |
---|---|
GB2094146B (en) | 1984-07-18 |
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