IE52144B1 - Triethylsulfonium salts of n-phosphonomethylglycine and their use as plant growth regulators and herbicides - Google Patents
Triethylsulfonium salts of n-phosphonomethylglycine and their use as plant growth regulators and herbicidesInfo
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- IE52144B1 IE52144B1 IE293681A IE293681A IE52144B1 IE 52144 B1 IE52144 B1 IE 52144B1 IE 293681 A IE293681 A IE 293681A IE 293681 A IE293681 A IE 293681A IE 52144 B1 IE52144 B1 IE 52144B1
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- phosphonomethylglycine
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Abstract
PROCEDURE FOR OBTAINING SALTS OF TRIALQUILSULFONIO OF N-PHOSPHONOMETILGLICINA REGULATORS OF VEGETABLE GROWTH, OF GENERAL FORMULA (I), IN WHICH N IS 0 OR 1 (CERTIFICATE OF ADDITION OF PATENT NUM. 506.605). CONSISTS IN MAKING N-PHOSPHONOMETILGLYCIN TO BE REACTED WITH SILVER OXIDE OR SODIUM HYDROXIDE, TO FORM THE CORRESPONDING SILVER OR SODIUM SALT, CONTINUATION IS ALREADY REACTIONED THIS LAST WITH AN OXIO-THIOULO-CHOICE CONTROLLING. OF INDESEABLE VEGETATION.
Description
This invention is directed to chemical compounds and their use in regulating the natural growth or developnent of plants. In particular, this invention relates to the chemical treatment of plants to alter their natural growth or developnent for the purpose of enhancing various agricultural or horticultural features of the plants, and also to the control of undesirable vegetation.
It is well known among those skilled in the art of agriculture and horticulture that various features of plant growth can be modified or regulated to produce a variety of beneficial effects.
' For instance, certain types of treatment can produce defoliation of a plant in a beneficial manner, I.e., inhibiting further leaf growth while permitting further developnent of the productive plant parts., As.-a-result, the productive parts demonstrate extra growth, and subsequent harvesting operations are facilitated. Defoliants are parti15 cularly useful in flax, cotton, and bean crops, and other crops of a similar nature. Although defoliation results In the killirg of leaves, it is not a herbicidal action per se since the remainder of the plant is unharmed. Indeed, killing of the treated plant is undesirable when defoliation is sought, since leaves will continue to adhere to a dead plant.
Another response demonstrated by plant growth regulants is the general retardation of vegetative growth. This response has a wide variety of beneficial features. In certain plants it causes a diminution - 3 or elimination of the normal apical dominance, and thus leads to a shorter train stem and Increased Lateral branching, 'litis alteration of the natural growth or developnent produces smaller, bushier plants which often demonstrate increased resistance to drought and pest infestation.
Die retardation of vegetative growth in turf grasses is particularly desirable. When the vertical growth rate of such grasses is lessened, root development is enhanced and a denser, sturdier turf is produced.
Die retardation of turf grasses also serves to increase the interval between mowings of lawns, golf courses and similar grassy areas.
Da many types of plants, such as silage crops, potatoes, sugar cane, beets, grapes, melons and fruit trees, the retardation of vegetative growth results in an increase in the carbohydrate content of the plants at harvest. It is believed that the retardation or suppression of such growth at the appropriate stage of development causes less of the available carbohydrate to be consumed for vegetative growth and results in an enhanced starch and/or sucrose content. Retardation of vegetative growth in fruit trees is demonstrated by shorter branches and greater fullness of shape, and often results in lesser vertical elongation.
Diese factors contribute to the ease of access to the orchard and simpli20 fy the fruit harvesting procedure.
It has now been discovered that triethylsulf(ox)onium salts of N-phosphonomethylglycine are useful in both regulating the natural growth or development of plants and in controlling undesirable vegetation. Diese salts have the formula (C2H5).3S(0)n© © 0 0 0 P-CH2NHCH2COH HO where n is zero or one.
Dels invention further relates to a method of regulating the natural growth or development of plants comprising applying to said - 4 plants an effective, plant-regulating, non-lethal amount of the above compounds, as well as a method of controlling undesirable vegetation comprising applying a herbicidally effective amount of the compounds to such vegetation when the latter is in a postemergence state.
As employed herein, the tern natural growth or development designates the normal life cycle of a plant in accordance with its genetics and environment, in the absence of artificial external influences.
A preferred utility of the compounds is in increasing the sucrose yield of field grown sugarcane and sorghum. Ihe term regulating is used herein to denote the bringing about through chemical means of any temporary or permanent modification or variation from the normal life cycle short of killing the plant.
Ihe term herbicidally effective amount designates any amount of the compounds disclosed herein which will kill, a plant or any portion thereof. By plants is meant germinant seeds, emerging seedlings, and established vegetation, including roots and above-ground portions.
Herbicidal effects include killing, defoliation, desiccation, stunting, leaf burn, and dwarfing. Herbicidal effects are generally achieved at higher application rates than growth regulating effects.
More specifically, the present invention relates to the triethylsulfonium salts of glyphosate and the triethylsulfoxonium salts of glyphosate. - 5 In accordance with the present invention, regulation of the natural growth or development of plants is achieved by the direct application of a compound within the above formula or a formulation of such a conpound to the plants or to any of their above-ground portions at approximately A to 10 weeks prior to harvest. With properly controlled application, a growth regulating effect can be achieved without herbicidal results. The amount which constitutes an effective amount varies not only with the particular material selected for treatment, but also with the regulatory effect to be achieved,' the species of plant being treated and its stage of development, and whether a permanent or transient effect is sought. Other factors which bear upon the determination of an appropriate plant regulating amount include the manner of application and weather conditions such as temperature or rainfall. Growth regulation may arise from the effect of the compound on either the physiological processes or the morphology of the plant, or from both in combination or in sequence. Mcrphological changes are generally noticeable by observable changes in the size, shape, color or texture of the treated plant or any of its parts, as well as in the quantity of fruit or flowers produced.
Changes in physiological processes, on the other hand, occur within the treated plant and are usually hidden frcm the eye of an observer. Changes of this type most often occur in the production, location, storage or use of chemicals naturally occurring in the plant, such as hormones. Fhysiological changes may be visually detectable when followed by a change in morphology. In addition, numerous analytical procedures for determining the nature and magnitude of changes in the various physiological processes are known to those skilled in the art.
Hie compounds of the present invention serve to regulate the natural growth or development of treated plants in a number of diverse ways, and it is to be understood that each compound nay not produce identical regulatory effects on each plant species or at every rate of application. As stated above, responses will vary in accordance with the compound, the rate, the plant, etc. - 6 llerbicidal effects are achieved in a similar manner, and Che strength of the application can be varied to achieve the desired result.
Ihe compounds of this invention are readily prepared from N-phosphonomethylglycine by reacting the latter with silver oxide to form the silver salt or with sodium hydroxide to form the sodium salt, and treating either the silver or sodiun salt with a triethylsulfonium or -sulfoxonium halide. Alternatively, the glycine can be reacted directly with the triethylsulfonium or -sulfoxoniun halide in the presence of propylene oxide. N-Phosphonomethylglycine is a connercially available material known by the common name glyphosate. It can be prepared by the phosphonomethylation of glycine, the reaction of ethyl glycinate with formaldehyde and diethylphosphite, or the oxidation of the N-phosphinomethylglycine. Such methods are described in U.S. Patent No. 3,799,758 (Franz, March 26, 1974).
As illustrated in the examples which follow, the compounds of the invention can either regulate the natural growth or development of plants or kl.11 weeds. While regulatory responses are often desirable in their own right, their effect on crop economics is most often of primary significance. Ihus, increases in the yield of individual plants, increases in the yield per unit area, and reductions in the cost of harvesting and/or subsequent processing are all to be considered in assessing the consequence of an individual regulatory effect during the growth or development of a plant.
Hie specific examples which follow are presented as merely illustrative, non-limiting demonstrations of the preparation of the compounds of the present invention and of their effectiveness in regulating the growth of plants and in controlling undesirable vegetation. - 7 EXAMPLE 1 Mono-Triethylsulfonlum Salt of Glyphosate A reaction vessel was charged with 100 ml of water, 4.2 g (0.025 mole) of N-phosphonomethylglycine, and 6.2 g (0.025 mole) of triethylsulfonium iodide. The reaction mixture was heated to 50°C and stirred at this temperature for one hour. It was then cooled to 15°C and 15 ml of propylene oxide was added. The resulting mixture was stirred at room temperature for two hours, then washed with ether and phase separated. The aqueous phase was then stripped, redissolved in ethanol, dried with sodium sulfate and washed again with ether. The final yield was 7.5 g of a liquid with a refractive index of ηθ = 1.5197. The molecular structure of the product was confirmed by carbon-13 nuclear magnetic resonance and infrared spectroscopy as that of the mono-triethylsulfonium salt of N-phosphonomethylglycine.
EXAMPLE 2 This example demonstrates the postemergence herbicidal activity of the compound prepared in Example 1.
Aluninum planting flats measuring 15-2 x 22.9 x 8.9 cm were filled to a depth of 7.6 cm with loamy sand soil, containing 50 parts per million (ppm) each of the commercial fungicide cis-N[(trichloromethyl)thio/-4-cyclohexene-l,2-dicarboximide (Captan (trademark)) and 17-17-17 fertilizer (percentages of N-PjO^-^O) on a weight basis). Several news were impressed across the width of each flat and a variety of seeds of both grass and broadleaf weed species were planted, one species per row. The weed species used are listed below: Broadleaf weeds: A. Annual morning glory B. Cocklebur C. Jimsonweed D. Velvetleaf E. Mustard P. Nightshade Ipcmoea purpurea Xanthium sp.
Datura stramonium Abutilon theophrastl Brasslca sp.
Solanum sp.
Grasses: G. Yellow nutsedge Cyperus esculentus II. Downybrome Bromus tectorum I. Foxtail Setaria sp. J. Annual ryegrass Lolium multiflorum K. Watergrass Eohinoohloa crusgalli L. Shattercane Sorghum bicolor M. Wild oat Avena fatua Hie broad leaf species were seeded first, and the grasses were seeded four days later. Ample seeds of each species were planted to produce 20 to 50 seedlings per row after emergence, depending cn the size of each plant.
Eleven days after the grasses were seeded, the emerged seedlings of all species were sprayed with aqueous solutions of the test compound.
The solutions were prepared to such dilutions that a spray rate of 80 gallons per acre (750 liters per hectare) gave from 0.5 to 4.0 pounds of test compound per acre (0.56 to 4.48 kilograms per hectare) as desired for each test. Additional flats not treated at all were used as standards for measuring the extent of weed control in the treated flats.
Traanty-cne days later, the test flats were compared to the standards and the weeds in each row were rated visually in terms of percent control ranging from 07» to 1007, with 07 representing the same degree of growth as the same row in the standard and 1007 representing complete kill of all weeds in the row. All types of plant injury were taken into consideration. The results are shown in the following Table. - 9 HERBICIDAL TEST RESULTS Test Confound: N-phosphonomethylglycine, trlethylsulfonlum salt Application Percent Control _ Rate (lb/Α) Broadleaf feeds Grasses (kg/ha) A B C "T3" E F ΤΓ T" J K L M N 0.25 (0.28) 1 1 *· 50 35 40 65 60 25 45 100 80 75 50 45 0.5 (0.56) 55 65 40 55 80 90 60 80 ioo 90 95 100 75 1.0 (1.12) 80 80 55 65 85 95 75 . 100 100 100 100 100 90 2.0 (2.24) 85 100 65 90 90 100 85 100 100 100 100 100 95 3.0 (3.36) 100 100 90 100 100 100 95 100 100 100 100 100 100 METHODS OF APPLICATION Whether used as plant growth regulators or as herbicides, the compounds of the present invention are roost useful when applied directly to the plants subsequent to their emergence from the soil. Si use at an agricultural field site, the compounds are generally embodied in suitable formulations containing additional ingredients and diluent carriers to aid in their dispersal. Examples of such ingredients or carriers are water, organic solvents, dusts, granules, surface active agents, waterin-oil and oil-in-water emulsions, wetting agents, dispersing agents, and emulsifiers. The formulations generally take the fonn of dusts, solutions, emulsifiable concentrates, or wettable powders.
A. LUSTS Dusts are dense powder compositions which combine the active compounds with a dense, free-flowing solid carrier. They are intended for application in dry form and are designed to settle rapidly to avoid being windbome to areas where their presence is not desired.
The carrier may be of mineral or vegetable origin, and is preferably an organic or inorganic powder of high bulk density, low - 10 surface area, and low liquid absorptivity. Suitable carriers include micaceous talcs, pyrophyllite, dense kaolin clays, tobacco dust, and ground calcium phosphate rock.
Ihe performance of a dust is sometimes aided by the inclusion 5 of a liquid or solid wetting agent, of ionic, anionic, or nonionic character. -Preferred wetting agents include alkylbenzene and alkylnaphthalene sulfonates, sulfated fatty alcohols, amines or acid amides, long chain acid esters of sodium isothionate, esters of sodium sulfosuccinate, sulfated or sulfonated fatty acid esters, petroleun sulfonates, sulfon10 ated vegetable oils, and ditertiary acetylenic glycols. Dispersants are also useful in the same dust compositions. Typical dispersants include methyl cellulose, polyvinyl alcohol, lignin sulfonates, polymeric alkylnaphthalene sulfonates, sodium naphthalene sulfonate, polymethylene bisnaphthalenesulfcnate, and scdium-N-methyl-N-(long chain acid) taurates.
In addition, inert absorptive grinding aids are frequently included in dust compositions to aid in the manufacturing of the dust. Suitable grinding aids include attapulgite clay, diatomaceous silica, synthetic fine silica and synthetic calcium and magnesium silicates.
In typical dust conpositions, carriers are usually present in concentrations of from about 30 to 90 weight percent of the total composition. The grinding aid usually constitutes about 5 to 50 weight percent, and the wetting agent up to about 1.0 weight percent. Dispersants, when present, constitute up to about 0.5 weight percent, and minor amounts of anticaking and antistatic agents may also be present. The particle size of the entire composition is usually about 30 to 50 microns.
B. SOLUTIONS Aqueous solutions of the active compounds are prepared such that application at the rate of about 1 to about 200 gallons of solution per acre (about 9 to about 1875 liters per hectare) will provide the required amount of active ingredient. A small amount of non-phytotoxic surfactant typically between 0.05? and 0.5? by weight is usually Included - 11 to improve the wetting ability of the solution and thus its distribution over the plant surface. Anionic, cationic, nonionic, ampholytic, and zwitterionic surfactants are all useful in this regard.
Suitable anionic surfactants include alkali metal, anmonium, and amine salts of fatty alcohol sulfates having from 8-18 carbon atoms in the fatty chain and sodlun salts of alkyl benzene sulfonates having from 9 to 15 carbon atoms in the alkyl chain. Suitable cationic surfactants include dimethyl dialkyl quaternary ammoniun halides with alkyl chains of 8 to 18 carbon atoms. Suitable nonionic surfactants include polyoxyethylene adducts of fatty alcohols having 10 to 18 carbon atoms, polyethylene oxide condensates of alkyl phenols with alkyl chains of 6 to 12 carbon atoms and 5 to 25 moles of ethylene oxide condensed onto each mole of alkyl phenol, and polyethylene oxide condensates of sorbitan esters with 10 to 40 moles of ethylene oxide condensed onto each mole of sorbitan ester. Suitable ampholytic surfactants include secondary and tertiary aliphatic amine derivatives with one aliphatic substituent containing 8 to 18 carbon atoms and another containing an anionic watersolubilizing group such as a sulfate or sulfonate. Sodium-3-dodecylaminopropionate and sodium-3-dodecyl amino propane sulfonate are examples. Suitable zwitterionic surfactants include derivatives of aliphatic quaternary ammonium compounds with one aliphatic substituent containing 8 to 18 carbon atoms and another containing an anionic water-solubilizing group. Examples of are 3-(N,N-dimethyl-N-hexadecylanmonio)propane-l-sulfonate and 3-(N,N-dimethyl-N-hexadecylanmonio)-2-hydroxy propane-1sulfcnate.
C. EMULSIFIABLE CONCENTRATES Emulsifiable concentrates are solutions in which the active materials and an emulsifying agent are dissolved in a non-watermiscible solvent. Prior to use, the concentrate is diluted with water to form a suspended emulsion of solvent droplets.
Typical solvents for use in emulsifiable concentrates include weed oils, chlorinated hydrocarbons, and non-water-miscible ethers, esters, and ketones. - 12 Typical emulsifying agents are anionic or nonionic surfactants, or mixtures of the two. Examples include long-chain mercaptan polyethoxy alcohols, alkylaryl polyethoxy alcohols, sorbitan fatty acid esters, polyoxyethylene ethers with sorbitan fatty acid esters, polyoxyethylene glycol esters with fatty or rosin acids, fatty alkylol amide condensates, calcium and amine salts of fatty alcohol sulfates, oil-soluble petroleum sulfonates, or preferably mixtures of these anulsifying agents. Such emulsifying agents usually comprise about 1 to 10 weight percent of the total composition.
Typical emulsifiable concentrates contain about 15 to 50 weight percent active material, about 40 to 82 weight percent solvent, and about 1 to 10 weight percent emulsifier. Other additives such as spreading agents and stickers can also be included.
D. WETTABLE PO/iDERS Wettable powders are water-dispersible compositions containing the active material, an inert solid extender, and one or more surfactants to provide rapid wetting and prevent flocculation when suspended in water.
Suitable solid extenders include both natural minerals and materials derived synthetically frcm such minerals. Examples include kaolinites, attapulgite clay, montmorillonite clays, synthetic silicas, synthetic magnesium silicate and calciun sulfate dihydrate.
Suitable surfactants include both nonionic and anionic types, and function as wetting agents and dispersants. Usually one of each is included. Preferred wetting agents are alkylbenzene and alkylnaphthalene sulfonates, sulfated fatty alcohols, amines or acid amides, lorg chain acid esters of sodium isothionate, esters of sodium sulfosuccinate, sulfated or sulfonated fatty acid esters, petroleum sulfonates, sulfonated vegetable oils, and ditertiary acetylenic glycols. Preferred dispersants are methyl cellulose, polyvinyl alcohol, lignin sulfonates, polymeric alkylnaphthalene sulfonates, sodium naphthalene sulfonate, polymethylene bisnaphthalenesulfonate, and sodium-N-nethyl-N(long chain acid) taurates. - 13 Topical wettable powders contain 25 to 90 percent active material, 0.5 to 2.0 percent wetting agent, 0.25 to 5.0 percent dispersant, and from 9.25 to 74.25 weight percent inert extender. Frequently, 0.1 to 1.0 percent of the extender is replaced by a corrosion inhibitor and/or an antifoaming agent.
E. IN GENERAL In general, any conventional postemergence method of application can be used, including conmon dusting or spraying equipment. The amount of active ingredient which is effective in producing the desired result, be it herbicidal or growth-regulating, depends on the nature of the plant species to be controlled and the prevailing conditions. Herbicidal effects are usually achieved at 0.1 to 50 pounds active ingredient per acre (0.112 to 56 kg/ha), preferably 1 to 10 (1,12 to 11.2), while plant growth regulation is usually achieved at O.l to 20 pounds active ingredient per acre (0.112 tn 22.4 kg/ha), preferably O.5 to 5 (0.56 to 5.6). It will be readily apparent to one skilled in the art that compounds of lower activity will reguire a higher dosage than more active compjounds for the same degree of control.
Claims (11)
1. CLAIMS:1. A compound having the formula (C-H-)-S(O) ® θ 00 0 2 S 3 η χ|| „ P-CH-NHCH-COH z
2. 2 H0 Z in which n is zero or one. 52. A compound according to Claim 1 in which n is zero.
3. A process for the preparation of a compound as claimed in claim 1, which comprises reacting the sodium or silver salt of N - phosphonomethylglycine with a triethylsulfonium or sulfoxonium halide. 10
4. A process as claimed in claim 3, wherein the sodium or silver salt has been prepared by reacting sodium hydroxide or silver oxide with N - phosphonomethylglycine.
5. A process for the preparation of a compound as claimed in claim 1, which comprises reacting N - phosphonomethyl15 glycine with triethylsulfonium or sulfoxonium halide in the presence of propylene oxide.
6. A herbicidal composition comprising a herbioidally effective amount of a compound as claimed in Claim 1 or 2 and an inert diluent carrier. 20
7. A method of controlling undesirable vegetation comprising applying to the vegetation in postemergent state herbicidally effective amount of a compound as claimed in Claim 1 or 2 optionally in the form of a composition as claimed in Claim 6.
8. A process for the preparation of a compound of the 25 formula given and defined in Claim 1, substantially as hereinbefore described with particular reference to Example 1 of the accompanying Examples.
9. A compound of the formula given and defined in Claim 1, whenever prepared by a process claimed in any one of claims 30 3-5 and 8. -ΙδΙΟ.
10.A herbicidal composition according to Claim 6, substantially as hereinbefore described with particular reference to Example 2 of the accompanying Examples.
11. A method according to Claim 7 of controlling 5 undesirable vegetation, substantially as hereinbefore described with particular reference to the Example 2 of the accompanying Examples.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US06/324,283 US4384880A (en) | 1980-12-04 | 1981-11-25 | Trialkylsulfonium salts of N-phosphonomethyl-glycine and their use as plant growth regulators and herbicides |
Publications (2)
Publication Number | Publication Date |
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IE812936L IE812936L (en) | 1983-05-25 |
IE52144B1 true IE52144B1 (en) | 1987-07-08 |
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Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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IE293681A IE52144B1 (en) | 1981-11-25 | 1981-12-14 | Triethylsulfonium salts of n-phosphonomethylglycine and their use as plant growth regulators and herbicides |
Country Status (7)
Country | Link |
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JP (1) | JPS5892685A (en) |
BR (1) | BR8204012A (en) |
ES (2) | ES8502124A2 (en) |
IE (1) | IE52144B1 (en) |
PH (1) | PH17476A (en) |
PT (1) | PT74276B (en) |
RO (1) | RO88895A (en) |
Family Cites Families (1)
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US3101265A (en) * | 1961-03-06 | 1963-08-20 | Shell Oil Co | Method for preventing undesired plant growth |
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1981
- 1981-12-14 IE IE293681A patent/IE52144B1/en not_active IP Right Cessation
-
1982
- 1982-01-13 RO RO82106317A patent/RO88895A/en unknown
- 1982-01-13 PT PT7427682A patent/PT74276B/en not_active IP Right Cessation
- 1982-02-12 PH PH26868A patent/PH17476A/en unknown
- 1982-02-25 JP JP2823382A patent/JPS5892685A/en active Pending
- 1982-07-09 BR BR8204012A patent/BR8204012A/en unknown
- 1982-11-24 ES ES517645A patent/ES8502124A2/en not_active Expired
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1984
- 1984-07-16 ES ES534347A patent/ES534347A0/en active Granted
Also Published As
Publication number | Publication date |
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RO88895A (en) | 1986-04-30 |
IE812936L (en) | 1983-05-25 |
ES8604409A2 (en) | 1986-02-01 |
ES517645A0 (en) | 1984-12-16 |
ES534347A0 (en) | 1986-02-01 |
BR8204012A (en) | 1983-07-05 |
PT74276A (en) | 1982-02-01 |
JPS5892685A (en) | 1983-06-02 |
PH17476A (en) | 1984-09-03 |
ES8502124A2 (en) | 1984-12-16 |
PT74276B (en) | 1983-06-27 |
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