AU2021221827A1 - Highly Loaded Solo Cyclanilide Formulations - Google Patents

Highly Loaded Solo Cyclanilide Formulations Download PDF

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Publication number
AU2021221827A1
AU2021221827A1 AU2021221827A AU2021221827A AU2021221827A1 AU 2021221827 A1 AU2021221827 A1 AU 2021221827A1 AU 2021221827 A AU2021221827 A AU 2021221827A AU 2021221827 A AU2021221827 A AU 2021221827A AU 2021221827 A1 AU2021221827 A1 AU 2021221827A1
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Australia
Prior art keywords
cyclanilide
formulation
ethephon
cotton
solo
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AU2021221827A
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Andrew HORSFIELD
Peter Vaughan
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Adama Australia Pty Ltd
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Adama Australia Pty Ltd
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Priority to AU2021221827A priority Critical patent/AU2021221827A1/en
Priority to ARP220102275A priority patent/AR126861A1/en
Priority to PCT/AU2022/051040 priority patent/WO2023023812A1/en
Priority to AU2022332715A priority patent/AU2022332715A1/en
Publication of AU2021221827A1 publication Critical patent/AU2021221827A1/en
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    • 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
    • A01N53/00Biocides, pest repellants or attractants, or plant growth regulators containing cyclopropane carboxylic acids or derivatives thereof
    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01PBIOCIDAL, PEST REPELLANT, PEST ATTRACTANT OR PLANT GROWTH REGULATORY ACTIVITY OF CHEMICAL COMPOUNDS OR PREPARATIONS
    • A01P13/00Herbicides; Algicides
    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01PBIOCIDAL, PEST REPELLANT, PEST ATTRACTANT OR PLANT GROWTH REGULATORY ACTIVITY OF CHEMICAL COMPOUNDS OR PREPARATIONS
    • A01P21/00Plant growth regulators
    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01GHORTICULTURE; CULTIVATION OF VEGETABLES, FLOWERS, RICE, FRUIT, VINES, HOPS OR SEAWEED; FORESTRY; WATERING
    • A01G22/00Cultivation of specific crops or plants not otherwise provided for
    • A01G22/50Cotton
    • 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
    • A01N25/00Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
    • A01N25/02Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests containing liquids as carriers, diluents or solvents
    • 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
    • A01N25/00Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
    • A01N25/30Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests characterised by the surfactants
    • 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
    • A01N57/00Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds
    • A01N57/18Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-carbon bonds
    • A01N57/20Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-carbon bonds containing acyclic or cycloaliphatic radicals

Abstract

The invention provides a highly loaded stable solo cyclanilide formulation, in which cyclanilide is present in a concentration of at least 250 g ai/L or at least 250 g ai/kg. In some embodiments, the formulation of the invention is particularly useful as a 5 harvest aid in cotton crops. 22

Description

Highly Loaded Solo Cyclanilide Formulations
Technical Field
The invention relates to cyclanilide formulations. In particular, the invention is concerned with solo cyclanilide formulations which have advantages over prior art formulations.
Background Art
Cyclanilide (1-(2,4-dicholoroanilinocarbonyl) cyclopropanecarboxylic acid) is a plant growth
regulator that inhibits polar auxin transport.
Uses for cyclanilide include:
- application in cotton in a mixture with ethephon to promote boll opening, defoliation
and terminal regrowth;
- application in cotton in a mixture with mepiquat chloride to reduce plant height and
ensure a more manageable crop; and
- use in nurseries and plant production (ornamentals) to inhibit meristematic tissue,
reduce apical dominance and increase branching of trees.
Use rates of cyclanilide in cotton typically range between 29 to 225 g ai/ha when applied as a
defoliant and 3 to 5 g ai/ha when applied with mepiquat. In ornamentals, cyclanilide is used as
a dilute application in 5 to 200 mg ai/L of spray solution.
Formulations of cyclanilide generally include suspension concentrate (SC) co-formulations with either ethephon e.g., ethephon 720 g/L + cyclanilide 90 g/L SC or with mepiquat e.g., mepiquat
67 g/L + cyclanilide 22 g/L SC, for cotton or as a solo SC e.g., cyclanilide 240 g/L SC - formulation
for use in ornamentals.
Commercial cyclanilide formulations currently used in cotton are generally low concentration,
with less than 100 grams of cyclanilide per litre or kilogram of formulated product and in a fixed ratio with another active ingredient (AI) such as ethephon or mepiquat. Ethephon and
mepiquat have high water solubility and can be formulated in efficient, high loaded solo
formulations.
Co-formulations are usually suspension concentrates, with the cyclanilide in the dispersed
phase and the ethephon or mepiquat dissolved in water in the continuous phase. The
maximum loading achievable in a cyclanilide co-formulation is lower for both cyclanilide and the partner Al/s due to their different solubilities. Additionally, to apply cyclanilide in a more
active and efficient form such as an emulsifiable concentrate is more complicated and costly to co-formulate with ethephon or mepiquat, due to the need for suitable solvents to ensure
stability.
Emulsifiable concentrates (EC) of cyclanilide are mentioned in prior art, primarily in mixtures with other active ingredients. The concentration of EC formulations of cyclanilide are not
disclosed at high concentrations e.g., at or more than 100 g ai/L
Cyclanilide co-formulations may reduce the flexibility of uses of both cyclanilide and the partner Al/s. Depending on the situation, the need to add cyclanilide to an application of ethephon or mepiquat may not be required, because a solo (and high loaded) product would be sufficient.
For example, the addition of solo cyclanilide as a tank mix option in cotton, under specific situations with either mepiquat earlier in the season or ethephon close to harvest, provides
greater flexibility for the end user. Additionally, a solo formulation provides greater opportunity
to vary the dose applied, as the use of a fixed ratio in a co-formulation may not always be desirable, as lower rates of the partner Al/s may produce similar efficacy at a given cyclanilide
rate.
There is therefore a need to provide a solo cyclanilide formulation that is more highly loaded
than previously known and that can be formulated as either a liquid or solid formulation.
Reference to any prior art in the specification is not an acknowledgment or suggestion that this
prior art forms part of the common general knowledge in any jurisdiction or that this prior art could reasonably be understood, regarded as relevant, and/or combined with other pieces of prior art by a skilled person in the art.
Summary of the Invention
This invention provides a stable, high loaded solo cyclanilide formulation, wherein cyclanilide is
present in a concentration of at least 250 g ai/L or at least 250 g ai/kg.
The formulation of the invention may be any agriculturally acceptable formulation type,
including a suspension concentrate (SC), an emulsifiable concentrate (EC), a suspo-emulsion
(SE), an oil-dispersion (OD), a capsule-suspension (CS), a dispersible concentrate (DC), an oil-in water emulsion (EW), water soluble granules (SG), water dispersible granules (WG) and
emulsifiable granules (EG).
In preferred embodiments. The formulation is an SC or an EC.
In the embodiment where the formulation of the invention is an EC, it may include excipients
such as one or more of emulsifiers, solvents and anti-foaming agents. The embodiment is not limited to these.
In the embodiment where the formulation of the invention is an SC, it may include one or more adjuvants and one or more excipients such as one or more of chelating agents, dispersants, wetting agents, adhesive aids, humectants, rheology modifiers and anti-foaming agents. The embodiment is not limited to these.
It has been found that embodiments of the solo formulation of the invention may be advantageous when used for vegetative or fruiting management of cotton, including reducing
crop height, reducing internode length, destroying of terminal buds and improving yield and
quality.
It has also been found that embodiments of the solo formulation of the invention may be used as a harvest aid for cotton defoliation and boll opening.
Embodiments of a solo formulation of the invention may be used in tank mixtures with tank mix
partners such as, but not limited to, mepiquat for vegetative or fruiting management of cotton
or with thidiazuron, ethephon, herbicides, ammonium sulfate and other water conditioners and oil adjuvants used as a harvest aids for cotton.
In this use, it is preferred that when the tank mix partner is mepiquat, for a tank mix with high loaded vegetative or fruiting management cotton plant growth regulators, the concentration of
mepiquat is 250 g ai/L or more.
When solo cyclanilide in a tank mix, with harvest aid plant growth regulator/defoliant products
and a tank mix partner is ethephon, it is preferred that the concentration of ethephon is at least
900 g ai/L.
As used herein, except where the context requires otherwise, the term "comprise" and
variations of the term, such as "comprising", "comprises and "comprised", are not intended to exclude further additives, components, integers or steps.
Further aspects of the present invention described in the preceding paragraphs will become
apparent from the following description, given by way of embodiments and/or examples.
Detailed Description of Preferred Embodiments
Reference will now be made in detail to certain embodiments of the invention. While the invention will be described in conjunction with the embodiments and/or examples, it will be
understood that the intention is not to limit the invention to those embodiments/examples. On the contrary, the invention is intended to cover all alternatives, modifications, and equivalents,
which may be included within the scope of the present invention.
One skilled in the art will recognize many methods and materials similar or equivalent to those described herein, which could be used in the practice of the present invention. The present
invention is in no way limited to the methods and materials described. It will be understood that the invention disclosed and defined in this specification extends to all alternative
combinations of two or more of the features mentioned or evident from the text. All of these different combinations constitute various alternative aspects of the invention.
For the purposes of interpreting this specification, terms used in the singular will also include the plural and vice versa.
Example 1: Highly Loaded Cyclanilide EC Formulation
By way of example, an EC formulation containing a cyclanilide concentration of about 250 g/L
was prepared. The formulation was designated as AD-AU-1806. The components are as set out in Table 1:
Table 1: ADAMA AD-AU-1806 Components
Content Component Purposein Supplier g/L Formulation
250.50 Cyclanilide Technical 99.8% active ingredient Nutrichem
39.22 NANSA© EVM 70/2E emulsifier Huntsman Corporation
80.78 TERMUL© 200 emulsifier Huntsman Corporation
636.42 HALLCOMID© 1025 solvent Stepan Company USA
0.10 Gensil© 2000 antifoam Solvay Chemicals Pty Ltd
Details of the components are as set out in Table 2:
Table 2: Component Detail
Trade Name IUPAC NAME CAS#
Cyclanilide Technical 1-[(2,4- 5915-41-3 99.8 % dichlorophenyl)carbamoyl]cyclopropane -1-carboxylic acid
benzenesulfonic acid, C10-13- 90194-26-6 NANSA© EVM 70/2E (linear)alkyl derivs., calcium salt in 104-76-7 solvent 2-ethylhexanol
TERMUL© 200 oxirane, methyl-, polymer with 37251-69-7 oxirane, mono(nonylphenyl) ether
HALLCOMID© 1025 N,N-dimethyl 9-decanamide 1356964-77-6
Gensil© 2000 polydimethylsiloxane 63148-62-9
Method of Preparation.
Note: TERMUL 200 is solid at ambient temperatures and requires melting.
1. Heat the required amount of TERMUL 200 in a water bath at 60 °C and maintain it in a completely molten state prior to addition.
2. Add the HALLCOMID© 1025 into a suitable vessel equipped with a propeller type stirrer.
3. Commence mixing and add TERMUL 200.
4. Continue mixing and add Cyclanilide Technical. '5 5. Maintain mixing for 45 mins until the Cyclanilide Technical is completely dissolved.
6. Maintain mixing and add NANSA EVM 70/2E.
7. Maintain mixing and add the Gensil 2000. Continue mixing for a further 15 mins.
8. Confirm the active ingredient content by Analytical Method QCM-165.02
9. Adjust with HALLCOMID 1025 as required.
Cold Storage Stability.
After seeded cold storage for 7 days at 0 °C, the product was noted to be cloudy and viscous however no separation or crystallisation was observed. Upon equivalence to ambient temperature, the product returned to a clear liquid without requiring agitation.
Example 2: Highly Loaded Cyclanilide SC Formulation
By way of further example, an SC formulation containing a cyclanilide concentration of about 250 g/L was prepared. The formulation was designated as AD-AU-1807. The components are as
set out in Table 3:
Table 3: ADAMA AD-AU-1807 Components
Content Component Purposein Supplier g/L Formulation
250.50 Cyclanilide Technical 99.8% active ingredient Nutrichem
360.00 Citric Acid Monohydrate adjuvant Redox Pty Ltd
10.00 Ethylenediamine chelating agent Redox Pty Ltd Tetraacetic Acid
35.00 Kraftsperse 25M dispersant Ingevity Corporation USA
12.00 Geropon© SDS wetting agent Solvay Chemicals Pty Ltd
25.00 Geropon© T/36 dispersant Solvay Chemicals Pty Ltd
Content Component Purposein Supplier g/L Formulation
6.25 Agrimer TM 30 adhesion aid Ashland Specialty USA
50.00 Propylene Glycol humectant Redox Pty Ltd
4.00 Rheozan SH rheology modifier Solvay Chemicals Pty Ltd
2.00 Gensil© 2030 antifoam Solvay Chemicals Pty Ltd
520.25 Potable water continuous phase Potable water supply
Details of the components are as set out in Table 4:
Table 4: Component Detail
Trade Name IUPAC NAME CAS#
Cyclanilide Technical 99.8 % 1-[(2,4 5915-41-3 dichlorophenyl)carbamoyl]cyclopropane -1-carboxylic acid
Citric Acid Monohydrate 2-hydroxypropane-1,2,3- 5949-29-1 tricarboxylicacid hydrate Ethylenediamine Tetraacetic 2-[2-[bis(carboxymethyl)amino]ethyl- 60-00-4 Acid (carboxy methyl) amino]acetic acid
Kraftsperse 25M lignosulfonic acid, sodium salt, 68512-34-5 sulfomethylated
Geropon© SDS sodium dioctylsulphosuccinate 577-11-7
Geropon© T/36 sodium polycarboxylate 59233-52-2
Agrimer TM 30 1-ethenylpyrrolidin-2-one 9003-39-8
Propylene Glycol propane-1,2-diol 57-55-6
Rheozan SH succinoglycan (modified polysaccharide) 73667-50-2
Gensil© 2030 polydimethysiloxane aqueous emulsion 63148-62-9
Potable water water 7732-18-5
Method of Preparation
Note: Dissolution of the Citric Acid requires the use of water heated to 60 °C.
1. Charge the heated water into a suitable vessel equipped with a high shear saw tooth impeller.
2. Commence dispersing and add Citric Acid. Continue to disperse until complete dissolution.
3. Continue dispersing and add EDTA.
4. Continue dispersing and add Gensil 2030. 5. Continue dispersing and add Kraftsperse 25M.
6. Continue dispersing and add Geropon SDS. 7. Continue dispersing and add Geropon T/36.
8. Continue dispersing and add Agrimer 30. 9. Disperse on high speed for 30 mins until homogeneous and free from
agglomerates. 10. Continue dispersing and slowly incorporate the Cyclanilide Technical.
11. Disperse on high speed for 30 mins until homogeneous and free from
agglomerates. 12. Bead mill by recirculation through a Dyno©KD Grinding Mill or equivalent until
a CIPAC MT 187 measured mean particle size < 3.0 microns and 90 % < 8.0 microns is achieved.
13. Transfer the mill base into a separate vessel and when the level permits commence stirring on slow speed.
14. Prepare a premix of the Propylene Glycol and Rheozan SH. 15. Add the Propylene Glycol; Rheozan SH premix when the Cyclanilide SC mill base has completed milling. Maintain stirring for a further 30 mins to ensure
complete hydration. Conduct cyclanilide content analysis as per QCM-165.02
and adjust to with water to meet the specification as required.
Cold Storage Stability.
Following cold temperature storage for 7 days at 0 °C, the product was clear of
any crystalline residue when passed through a 75 im sieve.
These formulations were tested successfully in cotton for the following uses:
- defoliation and boll opening in tank mixtures with ethephon, thidiazuron and oil
adjuvants; and
- for control of fruiting and vegetative growth in a tank mixture with mepiquat.
Example 3: Field Trials
Field Trial 1: Narrabri, New South Wales, Australia, Site 1.
One small plot replicated field trial was conducted to evaluate experimental formulations for cotton defoliation. The trial was conducted near Narrabri in the Lower Namoi Valley region of
New South Wales, Australia.
Treatments were applied broadcast over the crop using a hand held boom incorporating
TT11015 flat fan nozzles. At an application speed of 1.5 metres per second and a pressure of 300 kPa, treatments were applied in a total volume of 134 L/ha and a medium quality. The trial
was established as a complete block design with three replicates. Plot size was 6 metres wide by 10 metres long. The crop was planted in a double skip row configuration, so each plot
consisted of 4 planted rows and 2 unplanted skip rows. All assessments were conducted on the
centre 2 planted rows.
The treatments and results are in Table 5.
At treatment, the crop was physiologically ready for defoliation. It was 1.2 to 1.5 m in height, with a heavy canopy density and 100% row closure between the adjacent planted rows. The
cotton plants also filled 50-60% of the one metre skip row space. With the heavy boll load plants were bent over which increased the canopy density with respect to spray penetration.
39% of bolls were open and natural senescence had commenced, with leaf discolouration and a low proportion of desiccated leaves present. The prevailing temperatures dictated that the defoliation conditions were "cold" according to industry guidelines.
Leaf drop on the untreated cotton continued over the duration of the trial, with the level being
20% at the final assessment made 11 days after application (DAA). At this time 76% of bolls
were open. This result reflected the physiological condition of the crop.
Detailed assessments were conducted pre-spray and, 4, 7 and 11 DAA. These included counts
of fresh and desiccated leaf, and bolls counts on the same marked plants in each plot.
Generally, all treatments increased the presence of desiccated/frozen leaf. No treatment improved boll opening over that which occurred naturally on the untreated
cotton.
Evaluations of AD-AU-1806 have demonstrated that the EC form of cyclanilide is highly active
when applied solo and can help defoliate cotton and increase boll opening. Additionally, solo
applications of cyclanilide can reduce cotton growth by reducing the number of nodes, crop height and terminal bud destruction.
When applied in combination with other cotton defoliants/boll openers such as thidiazuron and ethephon, AD-AU-1806 can improve defoliation and boll opening to a similar or superior level compared with thidiazuron tank mixed with an SC co-formulation of ethephon + cyclanilide.
This is demonstrated in Table 5, where the addition of AD-AU-1806 at a higher cyclanilide dose
(60 g ai/ha) with the lower rate of ethephon (238 g ai/ha) provided similar or greater defoliation and boll opening compared with the full ethephon dose (applied either as Escalate
500 + AD-AU-1804 or + AD-AU-1806 + Promote Plus 900).
AD-AU-1807 performed similarly to AD-AU-1806.
Table 5. Evaluation varying combinations of thidiazuron, ethephon and cyclanilide on cotton defoliation and boll opening cv. Sicot 754B3F. Narrabri, New South Wales, Australia
Active 14 days after application
Treatment ingredients) & Rate % % fresh % dessicated % bolls concentration (g ai/ha) defoliation leaves leaves open post (g/L) retained retained appln
Untreated - - 37.8 h 53.8 g 8.4 39.7
Ethephon 720 +
AD-AU-1804 Cyclanilide 90 238+30 63.0 c-g 25.3 c-f 11.8 53.8 SC
Ethephon 720 +
AD-AU-1804 Cyclanilide 90 482+60 67.5 b-f 20.9 a-d 11.6 51.8 SC
AD-AU-1806 Cyclanilide 250 60 53.3 g 31.7 f 15.0 59.9
Active 14 days after application
Treatment ingredients) & Rate % % fresh % dessicated % bolls concentration (g ai/ha) defoliation leaves leaves open post (g/L) retained retained appln
EC
AD-AU-1807 Cyclanilide 250 60 57.8 fg 31.1 ef 11.2 46.2 Sc
Escalate 500 Thidiazuron 500 75 60.0 d-g 28.5 def 11.5 47.3 SC* SC
Thidiazuron 500 Escalate 500 SC 75+238 SC + Ethephon 720 + +30 73.0abc 18.2 abc 8.8 51.0 AD-AU-1804 Cyclanilide 90 SC
Escalate 500 Thidiazuron 500 SC SC+ 75+482 Ethehon 720 + 69.9 a-e 21.6 b-e 8.5 44.3 AD-AU- p +60 1804* Cyclanilide 90 SC
Escalate 500 Thidiazuron 500 SC + SC + Ethephon Promote 900 SL + 75+238 67.5 b-f 21.9 b-e 10.6 38.3 Plus 900 + Cyclanilide 250 +30 AD-AU- C 1806*
Escalate 500 Thidiazuron 500 SC + SC + Ethephon Promote 900 SL + 75+238 68.7 a-f 18.9 abc 12.4 50.9 Plus 900 + Cyclanilide 250 +60 AD-AU- C 1806*
Escalate 500 Thidiazuron 500 SC + SC + Ethephon Promote 900 SL + 75+482 58.3 efg 31 ef 10.7 45.3 Plus 900 + Cyclanilide 250 +60 AD-AU EC 1806*
Escalate 500 Thidiazuron 500 75+238 SC + SC + Ethephon +30 68.4a-f 20.8 a-d 10.8 46.3 Promote 900 SL +
Active 14 days after application
Treatment ingredients) & Rate % % fresh % dessicated % bolls concentration (g ai/ha) defoliation leaves leaves open post (g/L) retained retained appln
Plus 900 + Cyclanilide 250 AD-AU- SC 1807*
Escalate500 Thidiazuron 500 SC + SC +Ethephon Promote S+Etehn 75 +238 +60 77.0 ab 15.5 ab 7.5 48.6 Plus900+ 900 SL + AD-AU- Cyclanilide 250 1807* SC
Escalate500 Thidiazuron 500
Promote SC + Ethephon 75+482 Plus 900 SL + +460 80.0 a 11.5 a 8.5 53.8 Plus 900 + Cylnle20 +60 AD-AU- Cyclanilide250 1807* SC
* Applied with D-C Tron oil adjuvant at 1 L/ha Means within the same column with a letter in common are not significantly different (P>0.05)
Field Trial 2: Brookstead, Queensland, Australia, Site 2
One small plot replicated field trial was conducted between April and May to evaluate experimental formulations for cotton defoliation. The trial was conducted near Brookstead in
the Inner Darling Downs region of Queensland, Australia.
Treatments were applied broadcast over the crop using a hand held boom incorporating
TT11001 flat fan nozzles. At an application speed of 1 metre per second and a pressure of 200 kPa, treatments were applied in a total volume of 117 L/ha and a medium quality. The trial was
established as a complete block design with three replicates. Plot size was 4 metres (rows) wide by 10 metres long.
At treatment, the crop was physiologically ready for defoliation. It was 1.0 to 1.2 m in height,
with medium canopy density, 70-90% row closure and 79% bolls open. Natural senescence had commenced with leaf discolouration and a low proportion of desiccated leaves present. Leaf
drop on the untreated cotton continued over the duration of the trial, with the level being 38% at the final assessment made 14 days after application (DAA). At this time 88% of bolls were open. This result reflected the physiological condition of the crop.
Detailed assessments were conducted pre-spray and 3, 8 and 14 DAA. These included counts of fresh and desiccated leaf, and bolls counts on the same marked plants in each plot. An
assessment of regrowth was made 14 DAA.
The treatments and results are set out in Table 6.
Cyclanilide did not provide defoliation of this cotton crop and did not appear to add to or
synergise the defoliant activity of ethephon.
When applied alone, both cyclanilide and ethephon generally enhanced boll opening over that
occurring naturally on the untreated cotton. Combinations of AD-AU-1806 or AD-AU-1807 with thidiazuron an ethephon enhanced boll opening.
No differences in regrowth were observed.
Table 6. Evaluation varying combinations of thidiazuron, ethephon and cyclanilide on cotton defoliation and boll opening cv. Sicot 746B3F. Brookstead, Queensland, Australia
14 days after application Active Treatment ingredient(s) & Rate % %fresh % % bolls concentration (g ai/ha) defoliati leaves dessicated open post (g/L) on retained leaves appln retained
Untreated - - 38.3 efg 60.7 fg 1a 27.4 e
AD-AU-1804 ycanide90 SC 238+30 53.6 c-f 43.8 c-f 2.6 ab 75.5 a-d
AD-AU-1804 ycanide90 SC 482+60 57.2 b-f 36.9 b-f 5.9 cde 80.7 abc
AD-AU-1806 Cyclanilide 250 EC 60 37.3 fg 56.2 efg 6.5 e 67.7 a-d
AD-AU-1807 Cyclanilide 250 SC 60 27.2 g 68.7 g 4 b-e 58.5 b-e
Escalate 500 Thidiazuron 500 SC 75 71.7 a-d 26.1 a-d 2.2 ab 49.4 cde SC*
Escalate 500 Thidiazuron 500 SC + 75 +238 SC + Ethephon 720 + +30 50.3 d-g 46.6 d-g 3.1 a-d 75.6 a-d AD-AU-1804 Cyclanilide 90 SC
14 days after application Active Treatment ingredient(s) & Rate % %fresh % % bolls concentration (g ai/ha) defoliati leaves dessicated open post (g/L) on retained leaves appln retained
Escalate 500 Thidiazuron 500 SC SC + E n+460 75 +482 Ethephon 720 + 62.3 a-e 35.2 a-e 2.6 ab 74.2 a-d +60
AD-AU-1804* Cyclanilide 90 SC
Escalate 500 Thidiazuron 500 SC SC + Promote + Ethephon 900 SL 75+238 66.2 a-d 28.3 a-d 5.5 cde 65.5 a-d Plus 900 + AD- + Cyclanilide 250 +30 AU-1806* EC
Escalate 500 Thidiazuron 500 SC SC + Promote + Ethephon 900 SL 75+238 77.4 abc 17.8 ab 4.8 b-e 83.9 ab Plus 900 + AD- + Cyclanilide 250 +60 AU-1806* EC
Escalate 500 Thidiazuron 500 SC SC + Promote + Ethephon 900 SL 75+482 73.9 a-d 20.2 abc 5.9 de 78.2 abc Plus 900 + AD- + Cyclanilide 250 +60 AU-1806* EC
Escalate 500 Thidiazuron 500 SC SC + Promote + Ethephon 900 SL 75+238 78.7 ab 15.3 ab 6e 44.5 de Plus 900 + AD- + Cyclanilide 250 +30 AU-1807* SC
Escalate 500 Thidiazuron 500 SC SC + Promote + Ethephon 900 SL 75+238 75.5 abc 19 ab 5.5 cde 43.1 de Plus 900 + AD- + Cyclanilide 250 +60 AU-1807* SC
Escalate 500 Thidiazuron 500 SC SC + Promote + Ethephon 900 SL 75+482 78.6 ab 15.1 ab 6.3 e 90.6 ab Plus 900 + AD- + Cyclanilide 250 +60 AU-1807* SC
* Applied with D-C Tron oil adjuvant at 1 L/ha Means within the same column with a letter in common are not significantly different (P>0.05)
Field Trial 3: Macalister, Queensland, Australia, Site 3
A similar trial was carried out at this site. The treatments and results are shown in Table 7,
below.
Table 7: Evaluation varying combinations of thidiazuron tank mixtures on cotton defoliation and boll opening cv. Sicot 748B3F. Macalister, Queensland, Australia Site 3 14 days after application Active Rate ingredient(s) & % %fresh % %bolls Treatment concentration (g defoliation leaves dessicated open post (g/L) ai/ha) retained leaves application retained
Untreated - - 44.5 fg 29.4 a 26.1 a 6.3 c
Escalate 500 + Thidiazuron 500 50+ SC + Ethephon 720 67.8 c-g 12.1 a 20.1 a 13.8 bc Promote 1000* 1000 SL
Thidiazuron 500 Escalate 500 + AD- SC + Cyclanilide 50+ AU-1806 + 250 EC + 90+ 83.2 abc 5.2 a 11.5 a 37.9 a Promote 1000* Ethephon 1000 720 SL
Application of AD-AU-1806 in the tank mix with Escalate 500 + Promote improved defoliation
and boll opening. The addition of AD-AU-1806 to Escalate 500 + Promote as significantly improved boll opening.
Field Trial 4: Macalister, Queensland, Australia, Site 4
A similar trial was carried out at this site. The treatments and results are shown in Table 8,
below. Table 8: Evaluation varying combinations of thidiazuron tank mixtures on cotton defoliation and boll opening cv. Sicot 748B3F. Macalister, Queensland, Australia 2021. Site 4.
14 days after application Active Rate Treatment ingredient(s) & % %fresh % %bolls concentration (g defoliation leaves dessicated open post (g/L) ai/ha) retained leaves application retained
Untreated - - 47.9 f 36.0 e 16.1 bc 34.5 a-d
Escalate 500 + Thidiazuron 500 50+ SC + Ethephon 720 84.2 ab 7.8 ab 8.0 a 41.3 a-d Promote 1000* 1000 SL
14 days after application Active Rate Treatment ingredient(s) & % %fresh % % bolls concentration (g defoliation leaves dessicated open post (g/L) ai/ha) retained leaves application retained
Thidiazuron 500 Escalate 500 + AD- SC + Cyclanilide 50+ AU-1806 + 250 EC + 90+ 86.3 a 5.2 a 8.5 a 48.0 a Promote 1000* Ethephon 1000 720 SL
*Applied with Hasten adjuvant at 0.5 L/ha Means within the same column with a letter in common are not significantly different (P>0.05)
Application of AD-AU-1806 in the tank mix with Escalate 500 + Promote improved defoliation
and boll opening compared with Escalate 500 + Promote.
Field Trial 5: Dalby, Queensland, Australia, Site 5
A vegetative growth trial was carried out at this site. The treatments and results are shown in Table 9, below.
Table 9. Evaluation of mepiquat and cyclanilide solo and tank mix applications for fruiting and vegetative growth management in cotton cv. Sicot 75BRF. Dalby, Queensland, Australia, Site 5.
Active Nodes above white Crop height increase Growth tip rating ingredient(s) flower (cm) (0-10)^ Treatment & Rate concentration (ai/ha) Pre- 4 WAA 7 WAA 4 WAA 7 WAA (g/L) spray 4 WAA
Untreated - - 4.1 2.2 cd 3.3 c 4.4 c 0.0 d 0.0 f
RX-380 Mepiquat 380 28.5 4.2 1.6 abc 0.0 a 1.0 ab 3.0 abc 5.3 bc SL
RX-380 Mepiquat 380 76 4.1 1.2 ab 0.2 ab 0.3 a 2.9 abc 6.7 ab SL
RX-380 Mepiquat 380 152 4.2 2.1 bcd 0.2 ab 0.6 a 2.5 bc 8.0 a SL
Active Nodes above white Crop height increase Growth tip rating ingredient(s) flower (cm) (0-10)A Treatment & Rate concentration (ai/ha) Pre- 4 WAA 7 WAA 4 WAA 7 WAA (g/L) spray 4 WAA
AD-AU-1806 Cyclanilide 10 3.7 1.8 abc 0.6 ab 0.9 a 2.5 bc 3.7 de 250 EC
AD-AU-1807 Cyclanilide 10 3.9 1.8 abc 1.4 b 3.1 bc 2.2 c 0.0 f 250 SC
Mepiquat 380 RX-380 + AD- SL+ 28.5+ 4.3 1.0 a 0.7 ab 2.0 ab 3.3 ab 4.3 cd AU-1806 Cyclanilide 10 250 EC
Mepiquat 380 RX-380 +AD- SL + 28.5 4.1 1.6 abc 0.2 ab 0.9 a 2.4 c 5.3 bc +
AU-1807 Cyclanilide 10 250 SC
0.806 0.014 0.004 0.017 <0.001 <0.001 F Probability
WAA = weeks after application Means within the same column with a letter in common are not significantly different (P>0.05) A0 = Green and Active Growing Tips, 10 = Dark and Burnt off Tips
There were significantly fewer nodes (NAWF) in the cotton treated with the mixture of AD-AU 1806 plus AD-AU-1815 than in the untreated cotton. By comparison, the solo application of AD
AU-1815 did not significantly reduce the number of nodes.
All treatments had a significant effect on crop growth at 4 WAA. The reduction in crop growth was also seen at 7 WAA with all treatments except AD-AU-1807 applied alone. All other
treatments had a similar effect on crop growth, including a solo application of AD-AU-1806.
All treatments had a significant effect on tip burn. Rate effects were seen with AD-AU-1815.
AD-AU-1806 applied solo reduced tip burn. The mixtures of AD-AU-1806 and AD-AU-1807 with AD-AU-1815 did not affect the level of tip burn seen compared with AD-AU-1815 applied alone.
Field Trial 6: Condamine, Queensland, Australia, Site 6
A similar trial was carried out at this site. The treatments and results are shown in Table 10,
below.
Table 10. Evaluation of mepiquat and cyclanilide solo and tank mix applications for fruiting and vegetative growth management in cotton cv. Sicot 75BRF. Condamine, Queensland, Australia 2019. Site 6.
Active Nodes above white Crop height increase Growth tip
Treatment ingredient(s) & Rate flower (cm) rating (0-1O)A concentration (ai/ha) (g/L) Pre-spray 3 WAA 3 WAA 7 WAA 3 WAA
Untreated - - 2.3 2.4 5.3 9.8 1.1 d
RX-380 Mepiquat 380 28.5 1.9 2.5 4.6 6.7 2.8 bc SL
RX-380 Mepiquat 380 76 2.2 2.1 3.2 6.0 4.1 a SL
RX-380 Mepiquat 380 152 2.1 2.4 3.5 6.2 3.0 bc SL
AD-AU-1806 Cyclanilide 250 10 1.7 2.3 3.5 7.2 3.4 abc EC
AD-AU-1807 Cyclanilide 250 10 2.2 2.5 3.7 8.0 2.5 c Sc
Mepiquat 380 RX-380 + AD- SL+ 28.5+10 1.7 3.0 2.5 6.3 3.7 ab AU-1806 Cyclanilide 250 EC
Mepiquat 380 RX-380 + AD- SL+ 28.5+10 2.0 2.8 4.2 5.7 3.4 abc AU-1807 Cyclanilide 250 SC
F Probability NS NS NS NS <0.001
WAA = weeks after application Means within the same column with a letter in common are not significantly different (P>0.05) A0 = Green and Active Growing Tips
The only treatment effect seen was in the colour grading of the crop tips which may indicate some tip burn off. AD-AU-1806 and AD-AU-1807 applied solo provided a similar level of tip
burn to both the AD-AU-1815 and AD-AU-1815 + AD-AU-1806 or AD-AU-1807.

Claims (12)

Claims
1. A stable, high loaded solo cyclanilide formulation, wherein cyclanilide is present in a concentration of at least 250 g ai/L or at least 250 g ai/kg.
2. The formulation of claim 1, which is chosen from the type: suspension concentrate (SC), an emulsifiable concentrate (EC), a suspo-emulsion (SE), an oil-dispersion (OD), a capsule-suspension (CS), a dispersible concentrate (DC), an oil-in-water emulsion (EW), water soluble granules (SG), water dispersible granules (WG) and emulsifiable granules (EG).
3. The formulation of claim 2, which is a suspension concentrate (SC) or an emulsifiable concentrate (EC).
4. The formulation of claim 3 which an EC and which includes excipients such as one or more of emulsifiers, solvents and anti-foaming agents.
5. The formulation of claim 3 which an SC and which include one or more adjuvants and one or more excipients such as one or more of chelating agents, dispersants, wetting agents, adhesive aids, humectants, rheology modifiers and anti-foaming agents.
6. The formulation of any one of claims 1 to 5, when combined in a tank mix with mepiquat.
7. The formulation of claim 6, wherein concentration of mepiquat is 250 g ai/L or more.
8. The formulation of any one of claims 1 to 5, when combined in a tank mix with ethephon.
9. The formulation of claim 8, wherein concentration of ethephon is at least 900 g ai/L
10. The formulation of any one of claims 1 to 5 when combined in a tank mix with one or more of thidiazuron, ethephon, herbicides, ammonium sulfate, water conditioners and oil adjuvants.
11. A method for vegetative or fruiting management of a cotton crop, including applying to the cotton crop the formulation as claimed in any one of claims 1to 10.
12. A method for aiding for cotton defoliation and/or boll opening in a cotton crop,
including applying to the cotton crop the formulation as claimed in any one of claims 1
to 10.
AU2021221827A 2021-08-25 2021-08-25 Highly Loaded Solo Cyclanilide Formulations Pending AU2021221827A1 (en)

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PCT/AU2022/051040 WO2023023812A1 (en) 2021-08-25 2022-08-25 Highly loaded solo cyclanilide formulations
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DE19911165B4 (en) * 1999-03-12 2008-03-13 Bayer Cropscience Ag defoliants
US9919979B2 (en) * 2005-01-21 2018-03-20 Bayer Cropscience Lp Fertilizer-compatible composition
US20130244876A1 (en) * 2012-03-14 2013-09-19 Thorsten Jabs Synergistic compositions comprising ethephon and saflufenacil or cyclanilide and saflufenacil
CN106472545A (en) * 2016-09-28 2017-03-08 江苏辉丰农化股份有限公司 One plant growth regulators
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