GB2225946A - Stabilized fungicidal composition - Google Patents

Stabilized fungicidal composition Download PDF

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Publication number
GB2225946A
GB2225946A GB8928089A GB8928089A GB2225946A GB 2225946 A GB2225946 A GB 2225946A GB 8928089 A GB8928089 A GB 8928089A GB 8928089 A GB8928089 A GB 8928089A GB 2225946 A GB2225946 A GB 2225946A
Authority
GB
United Kingdom
Prior art keywords
benzamide
composition
fungicidal composition
phthalimide
ethoxy
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.)
Withdrawn
Application number
GB8928089A
Other versions
GB8928089D0 (en
Inventor
David Seaman
Peter John Vernon Cleare
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.)
Imperial Chemical Industries Ltd
Original Assignee
Imperial Chemical Industries Ltd
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 Imperial Chemical Industries Ltd filed Critical Imperial Chemical Industries Ltd
Publication of GB8928089D0 publication Critical patent/GB8928089D0/en
Publication of GB2225946A publication Critical patent/GB2225946A/en
Withdrawn legal-status Critical Current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
    • 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
    • A01N25/32Ingredients for reducing the noxious effect of the active substances to organisms other than pests, e.g. toxicity reducing compositions, self-destructing compositions
    • 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
    • A01N25/22Biocides, 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 ingredients stabilising the active ingredients
    • 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
    • A01N37/44Biocides, 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 at least one carboxylic group or a thio analogue, or a derivative thereof, and a nitrogen atom attached to the same carbon skeleton by a single or double bond, this nitrogen atom not being a member of a derivative or of a thio analogue of a carboxylic group, e.g. amino-carboxylic acids
    • A01N37/46N-acyl derivatives

Landscapes

  • Life Sciences & Earth Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Dentistry (AREA)
  • Plant Pathology (AREA)
  • Engineering & Computer Science (AREA)
  • Pest Control & Pesticides (AREA)
  • Agronomy & Crop Science (AREA)
  • Wood Science & Technology (AREA)
  • Zoology (AREA)
  • Environmental Sciences (AREA)
  • Toxicology (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)

Abstract

A plant fungicidal composition comprises N-(trichloromethylthio)phthalimide or the 1, 2, 3, 6-tetrahydrogenated product thereof, (RS) chloro-N-[cyano(ethoxy)methyl] benzamide, and a copper salt or compound which reduces emission of HCN from the composition on storage.

Description

FUNGICIDAL COMPOSITIONS The present invention relates to fungicidal compositions and to their use in combating fungi, especially fungal infections of plants.
According to the present invention there is provided a fungicidal composition comprising N-(trichloromethylthio)phthalimide or the 1, 2, 3, 6-tetrahydrogenated product thereof, (RS)-4-chloro-N -[cyano(ethoxy)methyl] benzamide and a copper salt or compound.
The N-(trichloromethylthio)phthalimide or its 1, 2, 3, 6-tetrahydrogenated product used in the composition of the invention include the fungicides commonly known as folpet and captan. Folpet has the formula
and its fungicidal properties are described by A R Kittleson in Science, 1952, 115, 84. Captan has the formula
and its fungicidal properties are described by W D Thomas et al in Photopathology, 1962, 52, 754. Of particular interest are the compositions containing folpet.
The compound (RS)-4-chloro-N- [cyano(ethoxy)methyl] benzamide having the formula:
and methods for preparing it are described and its use as a fungicide proposed in EP-A-0059536.
The copper salt or compound may be a copper(I) or copper(II) salt or compound, for example, cuprous chloride, cuprous oxide or cupric oxide, or a mixture thereof.
In one particular aspect the present invention provides a fungicidal composition comprising N -(trichloromethylthio)phthalimide, (RS)-4-chloro-N -[cyano(ethoxy)methyl] benzamide and cuprous chloride, cuprous oxide or cupric oxide.
It has been found that the presence of the copper salt or compound reduces the emission of hydrogen cyanide from the composition, believed to be produced by decomposition of the benzamide component on storage.
Suitable compositions are those in which the proportion by weight of the phthalimide to benzamide is from 3 to 80 : 1, more suitably from 5 to 40 : 1 and typically from 8 to 14 : 1.
The amount of copper salt or compound used is suitably from 0.01 to 10% by weight of the combined weight of phthalimide and benzamide, more suitably 0.2 to 5% and typically about 1%.
The compositions will normally be in the form of wettable powders but may also be in the form of water dispersible granules, suspension concentrates or dust or seed treatments.
Wettable powders, water dispersible granules and suspension concentrates will normally contain surfactants eg. a wetting agent or dispersing agent.
These agents can be cat ionic, anionic or non-ionic agents.
Suitable cat ironic agents are quaternary ammonium compounds, for example cetyltrimethylammonium bromide. Suitable anionic agents are soaps, salts of aliphatic monoesters of sulphuric acid (for example sodium lauryl sulphate), and salts of sulphonated aromatic compounds (for example sodium dodecylbenzenesulphonate, sodium, calcium or ammonium lignosulphonate, butylnaphthalene sulphonate, and a mixture of sodium diisopropyl- and triisopropylnaphthalene sulphonates), naphthalene sulphonate formaldehyde condensates and sodium di-octyl and di-nonyl sulphosuccinates.
Suitable non-ionic agents are the condensation products of ethylene oxide with fatty alcohols such as oleyl or cetyl alcohol, or with alkyl phenols such as octyl- or nonylphenol and octylcresol. Other non-ionic agents are the partial esters derived from long chain fatty acids and hexitol anhydrides, the condensation products of the said partial esters with ethylene oxide, and the lecithins.
Wettable powders and water dispersible granules also contain a solid diluent or carrier such as kaolin, kieselguhr, dolomite, calcium carbonate, talc, magnesium carbonate and diatomaceous earth.
Water dispersible granules can contain disintegrants which may be water soluble salts such as sodium acetate or sodium sesquicarbonate.
Compositions for use as aqueous dispersions are generally supplied in the form of suspension concentrates containing a high proportion of the active ingredients, the concentrates being diluted with water before use. These concentrates should preferably be able to withstand storage for prolonged periods and after such storage be capable of dilution with water in order to form aqueous preparations which remain homogeneous for a sufficient time to enable them to be applied by conventional spray equipment. Suspension concentrates normally contain suspending agents. Suitable suspending agents are polymeric thickeners (for example xanthan gum and sodium carb- oxymethylcellulose), and swelling clays such as bentonite or attapulgite. The concentrates may conveniently contain up to 95%, suitably 10-90%, for example 25-80%, by weight of the active ingredients.After dilution to form aqueous preparations, such preparations may contain varying amounts of the active ingredients depending upon the intended purpose, but an aqueous preparation cotaining 0.0005% or 0.01% to 10% by weight of active ingredients may be used.
The compositions of the invention are active fungicides and may be used to control a range of fungal diseases. Their uses include those described in EP-A-0059536 for the benzamide component and those for which folpet and captan are known to be used.
They may contain other compounds having biological activity, eg. compounds having similar or complementary fungicidal activity or which possess plant growth regulating, herbicidal or insecticidal activity. The invention also provides, therefore, a method of combating fungi, which comprises applying to a plant a fungicidally effective amount of the composition as herein defined.
The invention is illustrated by the following example: EXAMPLE A composition 'X' was prepared by mixing together the following ingredients: g/kq (RS)-4-chloro-N-[cyano(ethoxy)methyl] benzamide 45 folpet (technical material manufactured by Chevron, France) 500 Morwet D425 (dispersant) 50 Empicol LZ (wetter) 20 Silica K320 (flow aid) 50 China clay GTY (filler) to lkg Three identical compositions were prepared except that to these were added 10g/kg of (1) cuprous chloride, (2) cuprous oxide and (3) oxide.
For each composition, 300 gms were placed in a 1 litre narrow top glass bottle leaving about 400 to 500 mls ullage. The bottle was sealed with a plastic insert and the bottle top taped on securely. After two weeks storage at 500C the hydrogen cyanide concentration was measured using a Draeger or Gastec pump by piercing the plastic insert. The results are given in the table below.
TABLE
Composition i HCN concn. in ppm after 2 weeks at 50 C X 1 100 X + cuprous chloride 3 X + cuprous oxide 0 X + cupric oxide 0 These results show that the amount of hydrogen cyanide emitted from a composition containing (RS)-4 -chloro-N-[cyano(ethoxy)methyl] benzamide and folpet is reduced by the presence of any one of cuprous chloride, cuprous oxide or cupric oxide.

Claims (3)

1. A fungicidal composition comprising N -(trichloromethylthio)phthalimide or the 1, 2, 3, 6-tetrahydrogenated product thereof, (RS)-4 -chloro-N-[cyano(ethoxy)methyl] benzamide and a copper salt or compound.
2. A fungicidal composition as claimed in claim 1 comprising N-(trichloromethylthio)phthalimide, (RS)-4-chloro-N-[cyano(ethoxy)methyl] benzamide and cuprous chloride, cuprous oxide or cupric oxide.
3. A method of combating fungi which comprises applying to a plant a fungicidally effective amount of a composition of claim 1.
GB8928089A 1988-12-14 1989-12-12 Stabilized fungicidal composition Withdrawn GB2225946A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB888829119A GB8829119D0 (en) 1988-12-14 1988-12-14 Fungicidal compositions

Publications (2)

Publication Number Publication Date
GB8928089D0 GB8928089D0 (en) 1990-02-14
GB2225946A true GB2225946A (en) 1990-06-20

Family

ID=10648440

Family Applications (2)

Application Number Title Priority Date Filing Date
GB888829119A Pending GB8829119D0 (en) 1988-12-14 1988-12-14 Fungicidal compositions
GB8928089A Withdrawn GB2225946A (en) 1988-12-14 1989-12-12 Stabilized fungicidal composition

Family Applications Before (1)

Application Number Title Priority Date Filing Date
GB888829119A Pending GB8829119D0 (en) 1988-12-14 1988-12-14 Fungicidal compositions

Country Status (4)

Country Link
FR (1) FR2640118A1 (en)
GB (2) GB8829119D0 (en)
IT (1) IT1239476B (en)
ZA (1) ZA898882B (en)

Also Published As

Publication number Publication date
GB8829119D0 (en) 1989-01-25
FR2640118A1 (en) 1990-06-15
IT1239476B (en) 1993-11-02
GB8928089D0 (en) 1990-02-14
IT8922535A0 (en) 1989-11-29
ZA898882B (en) 1990-08-29
IT8922535A1 (en) 1991-05-29

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