AU643238B2 - Method for defoliating and desiccating cotton - Google Patents

Method for defoliating and desiccating cotton

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Publication number
AU643238B2
AU643238B2 AU67285/90A AU6728590A AU643238B2 AU 643238 B2 AU643238 B2 AU 643238B2 AU 67285/90 A AU67285/90 A AU 67285/90A AU 6728590 A AU6728590 A AU 6728590A AU 643238 B2 AU643238 B2 AU 643238B2
Authority
AU
Australia
Prior art keywords
cotton
compound
defoliating
desiccating
composition
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.)
Ceased
Application number
AU67285/90A
Other versions
AU6728590A (en
Inventor
Billy R. Corbin Jr.
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Valent USA LLC
Original Assignee
Valent USA LLC
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Valent USA LLC filed Critical Valent USA LLC
Publication of AU6728590A publication Critical patent/AU6728590A/en
Application granted granted Critical
Publication of AU643238B2 publication Critical patent/AU643238B2/en
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

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Classifications

    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION 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
    • A01N37/00Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
    • A01N37/18Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing the group —CO—N<, e.g. carboxylic acid amides or imides; Thio analogues thereof
    • A01N37/32Cyclic imides of polybasic carboxylic acids or thio analogues thereof
    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION 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
    • A01N39/00Biocides, pest repellants or attractants, or plant growth regulators containing aryloxy- or arylthio-aliphatic or cycloaliphatic compounds, containing the group or, e.g. phenoxyethylamine, phenylthio-acetonitrile, phenoxyacetone
    • A01N39/02Aryloxy-carboxylic acids; Derivatives thereof
    • A01N39/04Aryloxy-acetic acids; Derivatives thereof
    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION 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
    • A01N43/00Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/72Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
    • A01N43/84Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms six-membered rings with one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,4

Landscapes

  • 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)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)

Description

METHOD FOR DEFOLIATING AND DESICCATING COTTON
The present invention relates to a method of using N- aryl tetrahydrophthalimides for cotton foliage desiccation and defoliation.
The term "plant-growth regulating agents" generally refers to compounds which advantageously alter the normal growth pattern of plants. In the case of cotton, growth-regulating desiccants and defoliants are particularly desirable to facilitate picking of the cotton bolls. Such agents must desiccate and/or defoliate without harming the cotton bolls and preferably permit the continued growth of the bolls while acting on the foliage. Desirably, the growth regulator will cause the plant to both desiccate and defoliate, thus greatly facilitating picking.
Growth-regulating compounds typically have some degree of herbicidal activity when used in higher concentration, but the converse is rarely true. A number of tetrahydrophthalimides are known to have herbicidal activity, for example, U.S. Patent Nos. 4,792,605, 4,770,695, 4,640,707 and 4,484,941 disclose such herbicidal compounds. SUMMARY OF THE INVENTION
The plant-growth regulating compounds utilized in the method of the present invention are represented by the formulas I, II and III:
H2)4CH3
Ε The above compound II has an asymmetric carbon atom and hence exists as optical isomers. The respective optical isomers and mixtures thereof are represented by the above formula and are encompassed within the invention.
The compounds of the formulas I, II and III exhibit outstanding cotton desiccating and defoliating activity and do not harm the cotton bolls. The present invention provides compositions comprising a cotton defoliating and desiccating effective amount of the aforedescribed compounds and an agriculturally acceptable carrier. The invention also provides methods for desiccating and defoliating cotton which comprise treating growing cotton plants with a desiccating and defoliating effective amount of the aforedescribed compounds.
DESCRIPTION OF THE PREFERRED EMBODIMENT The compounds of the formulas I, II and III are known, and methods of synthesis and formulation are disclosed in Patent Nos. 4,792,605, 4,770,695, 4,640,707 and 4,484,941, which are incorporated herein by reference.
The compounds of the formulas (I) , (II) and (III) and their salts exhibit cotton plant desiccating and defoliating activity.
Typically, the above compounds are applied at a rate of about 1 to 100 grams, preferably about 5 to 40 grams per acre and are applied directly to the foliage of the cotton plant. Also, although in theory the compounds can be applied undiluted, in actual practice they are generally applied as a composition or formulation comprising an effective amount of the compound(s) and an acceptable carrier. An acceptable carrier (agriculturally acceptable carrier) is one which does not significantly adversely affect the growth-regulating effect achieved by the active compounds, save to dilute it, and does not significantly adversely affect the cotton bolls and is generally nontoxic to the environment in the amounts used. Typically, the composition contains about from 0.1% to 50% by weight of the compound of Formula (I) and/or (II) and/or (III) . Conveniently, formulations containing the compound of the formula (I) as active ingredient may be water- dispersible and contain up to about 50% weight/volume of active ingredient. Preferably, formulations containing the compound of the formula (I) or (II) as active ingredient may be flowable fluid concentrates containing up to about 20% weight/volume of active ingredient. Compound (III) is conveniently formulated as an emulsifiable concentrate typically containing up to 10% wt/vol. of Compound (III) . Concentrates can also be made having higher concentrations designed for dilution prior to application. The carrier can be a solid, liquid, or aerosol. The final compositions in field use can take the form of granules, powders, dusts, solutions, emulsions, slurries, aerosols, and the like, which may be suitably diluted with water for spraying.
Suitable solid carriers which can be used include, for example, natural clays (such as kaolin, attapulgite, montmorillonite, etc.), talcs, pyrophyllite, diatomaceous silica, synthetic fine silica, calcium aluminosilicate, tricalcium phosphate, and the like. Also, organic materials, such as, for example, walnut shell flour, cotton-seed hulls, wheat flour, wood flour, wood bark four, and the like can also be used as carriers. Suitable liquid diluents which can be used include, for example, water, organic solvents (e.g., hydrocarbons such as benzene, toluene, dimethylsulfoxide, kerosene, diesel fuel, fuel oil, petroleum naphtha, etc.), and the like. Suitable conventional aerosol carriers which can be used include conventional aerosol carriers such as halogenated alkanes, etc.
The composition can also preferably contain various promoters and surface-active agents which enhance the rate of transport of the active compound into the plant tissue such as, for example, organic solvents, wetting agents and oils (e.g. , paraffin oils) which can increase the ultimate desiccating or defoliating effect. The paraffin oil or wax can be conveniently used with the carrier (for example, water) at concentration of about from 0.25% to 5% by weight of the total composition. The surface-active agent can be anionic, cationic or non-ionic in character. The composition can also contain various compatible adjuvants, stabilizers, conditioners, insecticides, fungicides, and if desired, other compatible cotton growth-regulating compounds.
Plant-growth-regulating tests were made using the following methods.
Five-month old cotton plants were sprayed (spray volume: 10 gal./acre) with the defoliant materials applied as a foliar spray using a tractor boom C02-sprayer at 5.56 ph, 52 psi pressure, through X-12 hollow cone nozzles (9 nozzles spaced 20" apart, from a height of 18" above the cotton). The air temperature was 56'F, humidity 80%, soil temperature 53*F (unless otherwise indicated) and the foliage was still damp from dew (8:00 a.m.). The bolls were 70-75% open. The spray was prepared by mixing a formulation concentrate of Compound I, II or III with water containing 1% v/v of a commercial oil spreading agent. A water dispersible granular formulation concentrate or liquid flowable concentrate was used in the case of Compound I and a flowable concentrate was used in the case of Compound II. In the use of Compound III the spray was prepared from an emulsifiable concentrate of Compound III. TABLE 1 COMPARATIVE COTTON DEFOLIATION
% Cotton Defoliation:
1 through 6 were liquids of the active ingredient as a liquid in water containing 1% v/v Agridex (a commercial oil spreading agent) .
7 was a control (Control A) of Thidiazuron (a commercial cotton defoliant) in water containing 1% v/v Agridex.
8 and 9 were two active compound mixtures of compounds of the invention and Thidiazuron in water containing 1%
Agridex.
10 was a control (Control B) of DEF 6 (a commercial organophosphate cotton defoliant) as an emulsified concentrate.
LSD = the least significant difference between the data points. TABLE 2 COMPARATIVE COTTON LEAF DESICCATION
% Leaf Desiccation:
A = Thidiazuron, in water containing 1% v/v Agridex. B = DEF 6, emulsified concentrate, in water.
TABLE 5 COMPARATIVE FIRST CROP PICK
% of Total Cotton Crop Harvested On First Pick 34 Days After Appln.
58 87 86 88 86 87 88 89
88
90 27.2
TABLE 6
COMPARATIVE LEAF DESICCATION IN PRESENCE OF MORNING-GLORY
Cotton % Leaf Desiccation: grams 2 Days 4 Days Formulation a.i./A After Appln. After Appl .
0 43 60 65 57 43
30
Morning-glory
2 Days 4 Days
After Appln. After Appln.
0 45 58 63 63 50
50
DEF 6 = Commercial organophosphate defoliant.
GRAMOX = Gramoxone, PARAQUAT defoliant formulation sold by ICI. Formulation 16 is in water containing 0.25% v/v of X-77.
SOD = Commercial sodium chlorate. Formulation 17 is in water containing 1% v/v Agridex.
Air temp. 92"F, rel. humidity 69%, soil temperature
99βF.
Formulations 11 through 17 were applied as a spray
§ 20 gal./acre. Formulations 12 through 15 were applied in water containing 1% v/v Agridex.
Formulations 1 and 2 were a water dispersable formulation of the active ingredient (i-e. Compound I) containing 1X v/v Agridex (a coπiπercial oil spreading agent). Formulations 3 through 6 were liquids of the active ingredient (re
Compound II or III) applied in water containing 1X v/v Agridex (a coπmercial oil spreading agent).
Formulation 7 was a control of DEF-6 (a commercial organophosphate cotton defoliant) as an emulsifiable concentrate. Formulations 1 through 7 were applied as a foliar spray at 20 gal./acre. Air temperature 56βF, rel. humidity 94X, soil temp.
60°F. About 50 to 65X of harvestable bolls were open.
TABLE 8 COTTON LEAF DESICCATION
X eaf Desiccation
1 I 5 2426 2 I 10 2799 3 II 5 2892 4 II 10 3111 5 III 10 2332 6 III 20 2612 7 Control 680 2612 LSD 544
Tables 1 and 2 show that at application rates as low as 5 gm. active ingredient/acre of compounds of the invention (I or II) , cotton defoliation and leaf desiccation 17 days after application are comparable to that of Control B (at 680 gm/acre) and better than Control A (at 91 gm/acre) . At 7 days after application compounds I and II (at 5 gm/acre) are better than Control A and Control B.
Table 3 shows that at application rates as low as 5 gm./acre the compounds of the invention are comparable to both controls (respectively applied at 91 g./acre and 680 g./acre) .
Tables 4 and 5 show that Compound II applied at 5 gm/acre is comparable to the controls with respect to total cotton yield and percent of yield harvested on the first pick. Compound I is comparable to the controls when applied at a rate of 10 g./acre.
Table 6 shows comparative leaf desiccation of cotton and morning-glory, a weed which is a problem particularly at the time of cotton harvesting. The twining nature of morning-glory causes it to sprawl up the cotton plants and portions become harvested with the cotton. If the morning-glory is green, it imparts color to the cotton fibers, thus lowering the quality of the harvested product. Table 6 shows that Compound I, applied as low as 5 g./acre, is comparable or better than the controls (formulations 16 and 17) for desiccation of both cotton and morning-glory.
Tables 7, 8 and 9 show that Compound III also gave comparable cotton defoliation, desiccation and yield at 20 g/acre to 680 g/acre of the control desiccant.

Claims (11)

1. A cotton-plant defoliating-desiccating composition comprising an amount of an active ingredient selected from the group consisting of a compound of the formulas (I) , (II) and (III) , and mixtures thereof.
H2)4CH3
said amount being effective to desiccate and defoliate said cotton plants, and an agriculturally compatible carrier.
2. A composition according to Claim 1 wherein said active ingredient comprises a compound of the formula I.
3. A composition according to Claim 1 wherein said active ingredient comprises a compound of the formula II.
4. A composition according to Claim 1 wherein said active ingredient comprises a compound of the formula III.
5. A composition according to Claim 1 wherein said active ingredient comprises a mixture of compounds of the formulas I, II and III.
6. Amethod for defoliating and desiccating cotton plants comprising the step of applying to the foliage of said plants a defoliating and desiccating effective amount of a composition comprising a compound of the formula I
H
7. Amethod for defoliating and desiccating cotton plants comprising the step of applying to the foliage of said plants a defoliating and desiccating effective amount of a composition comprising a compound of the formula II
8. Amethod for defoliating and desiccating cotton plants comprising the step of applying to the foliage of said plants a defoliating and desiccating effective amount of a composition comprising a compound of the formula III
9. A method according to Claim 6, 7 or 8 wherein said composition comprises a defoliating anddesiccating effective amount of said compound.
10. A method according to Claim 9 wherein said compound is applied to said plants and their environment at a rate in the range of 1 to 100 grams per acre.
11. A method according to Claim 10 wherein said range is 5 to 40 grams per acre.
AU67285/90A 1989-10-31 1990-10-30 Method for defoliating and desiccating cotton Ceased AU643238B2 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US42941489A 1989-10-31 1989-10-31
US429414 1989-10-31

Publications (2)

Publication Number Publication Date
AU6728590A AU6728590A (en) 1991-05-31
AU643238B2 true AU643238B2 (en) 1993-11-11

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ID=23703140

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Application Number Title Priority Date Filing Date
AU67285/90A Ceased AU643238B2 (en) 1989-10-31 1990-10-30 Method for defoliating and desiccating cotton

Country Status (2)

Country Link
AU (1) AU643238B2 (en)
WO (1) WO1991006216A1 (en)

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4484941A (en) * 1981-09-01 1984-11-27 Sumitomo Chemical Company, Limited Tetrahydrophthalimides, and their production and use as herbicides

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4640707A (en) * 1984-07-23 1987-02-03 Sumitomo Chemical Company, Ltd. Tetrahydrophthalimides and their herbicidal use

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4484941A (en) * 1981-09-01 1984-11-27 Sumitomo Chemical Company, Limited Tetrahydrophthalimides, and their production and use as herbicides

Also Published As

Publication number Publication date
WO1991006216A1 (en) 1991-05-16
AU6728590A (en) 1991-05-31

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