GB2095557A - Pest repellant - Google Patents

Pest repellant Download PDF

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Publication number
GB2095557A
GB2095557A GB8209011A GB8209011A GB2095557A GB 2095557 A GB2095557 A GB 2095557A GB 8209011 A GB8209011 A GB 8209011A GB 8209011 A GB8209011 A GB 8209011A GB 2095557 A GB2095557 A GB 2095557A
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United Kingdom
Prior art keywords
alkylcarbamate
aversion
pest
effective amount
response
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Granted
Application number
GB8209011A
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GB2095557B (en
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Union Carbide Corp
Original Assignee
Union Carbide Corp
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Filing date
Publication date
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Publication of GB2095557A publication Critical patent/GB2095557A/en
Application granted granted Critical
Publication of GB2095557B publication Critical patent/GB2095557B/en
Expired 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
    • A01N47/00Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
    • A01N47/08Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
    • A01N47/10Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof
    • A01N47/22O-Aryl or S-Aryl esters thereof

Abstract

Substituted aryl alkylcarbamates have been found to provide outstanding pest repellancy when applied to desirable foliage or agronomic crops.

Description

SPECIFICATION Pest repellant This invention relates generally to the use of substituted aryl carbamates and, more particularly, trialkylphenyl alkylcarbamates, wherein each alkyl group has from 1 to 4 carbon atoms, in pest repellant compositions.
Animal pests that attack foliage or crops are a common problem for both the individual homeowner and the large-scale farmer. By way of illustration, rabbits enjoy eating Spiraea bushes in the wintertime when snow covers other potential food. Blackbirds prefer eating ripe cherries from the farmer's trees.
Such animals are particularly difficult to treat since they are desirable wildlife when not consuming agronomic crops or foliage. Proper treatment of such wildlife presumes that they be exposed only to relatively non-toxic substances, if possible.
Commercial products such as, for example, methiocarb have been developed to combat the above problems. It would be desirable, however, to develop a new bird and mammal repellant that is more effective than currently-available commercial pest-repellants and less hazardous to the repelled pest and non-target birds and other wildlife.
This invention relates to the use of trialkylphenyl alkylcarbamates in the control of agronomic and horticultural pests. The invention encompasses the use of pest-repellant compositions containing at least one of such compounds wherein each alkyl group has from 1 to 4 carbon atoms.
The compounds useful as active ingredients in the pest-repellant compositions used in the present invention include all trialkylphenyl alkylcarbamates wherein each alkyl group has from 1 to 4 carbon atoms. Preferred compounds within the scope of the present invention are 2,3,5trimethylphenyl methylcarbamate and 3,4,5-trimethylphenyl methylcarbamate, alone or in weight ratio mixtures of 1:9 to 9:1 of the 2,3,5- to 3,4,5-isomers. These compounds can be used alone or in mixtures thereof, or they can be mixed with conventional pest-repellant compounds to form the active portion of new pest repellant compositions. The compounds used in the present invention are made in accordance with the known methods of United States Patent 3,1 30,1 22 incorporated herein by reference.
The compounds useful as active ingredients in the present invention are employed in an amount sufficient to produce an aversion response in the bird or other animal pest to be controlled with respect to the particular foliage or crop to be treated. This amount will vary over a wide range and the required amount to induce an aversion response will depend upon a variety of factors such as the nature of the pest, the nature of the crop or foliage, climatic conditions at the time of treatment, etc. In general, however, preferred range of amounts of active carbamate in the carrier would be from 0.25 wt. percent to 10 wt. percent, more preferably from 0.5 percent to 1.0 percent depending on the type of formulation, based on wt.
% of active carbamate plus carrier.
As used herein, the term "pest repellant" is intended to encompass pest-aversion responses induced in the target pest by any mode including, but not limited to, oral ingestion, inhalation, injection into the blodstream, or by dermal application e.g. into the skin of the animal via application to the animal's perch.
Although not wishing to be bound by any particular theory, the compounds of the present invention are effective in producing a animal-pest aversion response after entering the blood- stream of the animal by conventional means.
Pest repellant compositions containing the above compounds as the active ingredient will usually comprise a carrier and/or diluent, either liquid or solid.
Suitable liquid diluents or carriers include water, petroleum distillates, or other liquid carriers with or without surface active agents. Liquid concentrates may be prepared by dissolving one of these compounds with a non-phytotoxic solvent such as acetone, xylene, or nitrobenzene and dispersing the active ingredient in water with the aid of suitable surface active emulsifying and dispersing agents.
The choice of dispersing and emulsifying agents and the amount employed is dictated by the nature of the composition and the ability of the agent to facilitate the dispersion of the active ingredient. Generally, it is desirable to use as little of the agent as is possible, consistent with the desired dispersion of the active ingredient in the spray so that rain does not re-emulsify the active ingredient after is is applied to the plant and wash it off the plant. Nonionic, anionic, amphoteric or cationic dispersing and emulsifying agents may be employed, for example, the condensation products of alkylene oxides with phenol and organic acids, alkyl aryl sulfonates, complex ether alcohols, or quaternary ammonium compounds.
In the preparation of wettable powder or dust or granualted compositions, the active ingredient is dispersed in and on an appropriately divided solid carried such as clay, talc, bentonite, diatomaceous earth, or fuller earth. In the formulation of the wettable powders the aforementioned dispersing agents as well as lignosulfonates can be included.
The required amount of the active ingredient contemplated herein may be applied per acre treated in from 1 to 3000 gallons or mote of liquid carrier and/or diluent or in from 5 to 7500 pounds of inert solid carrier and/or diluent. The concentration in the liquid concentrate will usually vary from 10 to 95 percent by weight and in the solid formulations from 0.5 to 90 percent by weight. Satisfactory sprays, dusts, baits, salves, lotions, suspensions, flowable liquids, emulsifiable concentrates, seed coatings paints or granules for general use contain from 1/4 to 1 5 pounds of active ingredient per acre.
When applied as seed treatments to protect crops from damage by birds and marhmals, the described compounds are preferably applied at rates ranging from 0.25 pounds to 1.0 pounds active ingredient per 100 pounds of seed.
When applied to growing or mature crops to protect them from damage by birds and mammals, the described compunds are preferably applied at rates ranging from 0.5-2.0 pounds active ingredient per 100 gallons of spray.
When applied as baits or as topical treatments. the described compounds are preferably applied at rates of 100 to 500 parts per million. Baits may contain the compound on the bait surface as with sunflower seeds for aversion of birds and rats or they may contain the compound in a manufactured edible solid or liquid substrate as a wax block containing grain or an oil or sugar-containing drink.
Typical modes of treatment with the active ingredients envisioned by the present invention include (a) post-emergent treatment of crops or foliage, (b) pre-emergent treatment of seed or seed-parts (e.g., tubers or sprouts), (c) granular application to the soil to produce an aversionresponse to the granule and (d) spray the harvested crops or incorporate into the pacakges for harvested crops to protect the crops from pests such as rodents via the aversion mechanism.
Mode (c) above could be used prior to the later application to the soil and crops of relatively toxic pesticides such as carbofuran in order to pre-condition avoidance of the granules by birds or other wildlife.
Other uses envisioned by the present invention include application to animals to protect them from injury by themselves or by others of the same species. For example, application of a suspension of active carbamate to the tails of pigs can protect them from being bitten by other pigs during shipment and reduce losses due to infected wounds. Similar applications would protect birds such as chickens and turkeys from "picking" and reduce the need for de-beaking or blinders. Addition of active carbamate to wound dressings would reduce chewing and licking of wounds by treated animals.
Application to mammals which have an oral component to pre-copulatory behaviour can prevent mating. Pest rodents such as rats, mice and squirrels can be controlled by this method.
For example, a box is rigged up to apply a dust or suspension of active carbamate to the hair of rodents which enter it to obtain food. Males and females so treated would not be expected to mate as a consequence of an aversion which is learned through licking other treated animals during precopulatory behaviour.
Th following examples are intended to illustrate, but not limit, the present invention: EXAMPLE I In order to demonstrate the effectiveness of ttSe pest-repellant compositions used in the present invention as compared with conmercial pest-repellant compositions, cherries were counted out on individuai, cherry trees and divided into three groups, each group containing 1 500 cherries, identified as Group A, Group B and Group C. Group A was sprayed with a pestcontrol composition used in the present invention wherein the active portion used a 1:6 wt. ratio mixture of 2,3, 5-trimethylphenyl methylcarbamate and 3,4, 5-trimethylphenyl methylcarbamate, and wherein the active mixture was applied in amount of three Ibs. active per acre. Group B was sprayed with a comparison pest-control composition, namely a commercial product, methiocarb, in an amount of three Ibs. active per acre. Group C, the control group, was not sprayed.
The results appear in Table I which follows: Table I Number of Cherries on Day Specified Day 1 Day 5 Day 12 Day 19 Group A 1500 963 698 0 Group B 1500 900 0 0 Group C 1500 0 O O EXAMPLE 11 In order to test the aversion response in wild red-winged blacltbirds with respect to untreated sunflowers bY vitue of exposure to treated fallen sunflower seeds, a 30.at3 meter X 1 5.24 meter field of Interstate Hybrid W897 sunflowers was enclosed with 1" hexagonal nylon mesh to provide 4 equal-sized enclosures 15.24M x 7.62M X 3.81M. Each enclosure contained 300 untreated flowers in 1 5 rows. ApproxiMately 35 wild trapped red-winged blackbirds were introduced into each enclosure. Damage to flower heads was assessed at weekly intervals for 5 weeks. Damage consisted of the percent of seeds 2 cm concentric arc removed from each flower head.
Approximately 2 kg of sunflower seeds and nuts treated with a 1:6 wt. ratio mixture of 2,3,5and 3,4,5-trimethylphenyl carbamate (0.5 gm/kg) were spread at the end of the first week and then weekly in two different enclosures. Untreated seeds and nuts were spread in the other 2 enclosures. Small piles of wheat screenlings and cracked corn were provided in each enclosure as an alternate food source.
The results indicated that percent of increase in head damage was decreased by 36.5% in the treated enclosures over the untreated check indicating that the birds learned to transfer their aversion from treated seeds on the groud to untreated seeds on the flower heads.
Comparable results were achieved using the same procedure and amounts of methiocarb.
However, the described carbamate mixture is much less toxic to birds than is methiocarb. For example, the LD50 (lethal dosage) for starlings of the above mixture is greater than 100 mg/kg, whereas the LD50 for methicarb is only 1 2 mg/kg.
EXAMPLE ill Norway rats were divided into 3 groups. Group A was exposed to a choice between untreated unpreferred unsweetened cornmeal and preferred sweetened corn meal that had been treated with the carbamate mixture of Examples I and II at a level of 40 ppm.
Group B was allowed to eat untreated sweetened corn meal followed by injection of 1 8 mg/kg of the same carbamate mixture.
Group C (control group) was given the choice between untreated sweetened corn meal and untreated unsweetened corn meal.
The results indicated that Group A consumed 75% of the amount of preferred food that was eaten by Group C whereas Group B consumed only 2% of the preferred food eaten by Group C.
Aversion was established by injection as well as by feeding the active mixture used in the present invention.

Claims (11)

1. A process for inducing an aversion response in bird or other animal pests to plants or unpicked fruit which comprises applying to the plants or unpicked fruit an effective amount of at least one trialkyphenyl alkylcarbamate, wherein each alkyl group has from 1 to 4 carbon atoms.
2. A process for producing an aversion response in animal pests with respect to agronomic crops which comprises contacting the bloodstream of the animal with an aversion-inducing effective amount of at least one trialkylphenyl alkylcarbemate, wherein each alkyl group has from 1 to 4 carbon atoms, wherein the effective amount is between 100 ppm and 500 ppm of the alkylcarbmate, and wherein the contacting is by oral ingestion, inhalation, injection or dermal application to the animal.
3. A pest-repellant method for treating agronomic seeds or seed-parts which comprises the pre-emergent treatment of the seeds or seed-parts wit;, an effective amount of at least one trialkylphenyl alkylcarbamate, wherein each alkyl group has from 1 to 4 carbon atoms.
4. A pest-repellant method for treating picked fruit or other agronomic crops which comprises contacting the picked fruit or crops, or a package therefor, with an effective amount of at least one trialkylphenyl alkylcarbamate, wherein each alkyl group has from 1 to 4 carbon atoms.
5. A process for inducing an aversion-response by animal pests to toxic pesticide granules which comprises, prior to treating soil with the toxic granules, applying to the soil placebo granules containing an aversion-effective amount of at least one trialkylphenyl alkylcarbamate, wherein each alkyl group has from 1 to 4 carbons.
6. A process as claimed in any one of claims 1, 3, 4, or 5 wherein the effective amount is between 1/4 pound and 1 5 pounds of the alkylcarbamate per acre treated.
7. A process as claimed in any one of claims 1 to 5 wherein the alkylcarbamate is 2,3,5trimethylphenyl methylcarbamate, or 3,4, 5-trimethylphenyl methylcarbamate, or a mixture thereof.
8. A process as claimed in any one of claims 1 to 5 wherein the alkylcarbamate is applied in a pest-repellant composition consisting essentially of the alkylcarbamate plus a carrier, wherein the alkylcarbamate is present in the composition in an amount of between 0.25 weight percent and 10 weight percent, based on the total weight of the composition.
9. A process for inducing an aversion response in bird or other animal pests to plants or unpicked fruit substantially as hereinbefore described.
10. A process for producing an aversion response in animal pests with respect to agronomic crops substantially as hereinbefore described.
11. A pest-repellant method for treating agronomic seeds or seed-parts substantially as hereinbefore described.
1 2. A pest-repellant method for treating picked fruit or other agronomic crops substantially as hereinbefore described.
1 3. A process for inducing an aversion-response by animal pests to toxic pesticide granules substantially as hereinbefore described.
GB8209011A 1981-03-27 1982-03-26 Pest repellant Expired GB2095557B (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US24824781A 1981-03-27 1981-03-27

Publications (2)

Publication Number Publication Date
GB2095557A true GB2095557A (en) 1982-10-06
GB2095557B GB2095557B (en) 1985-08-07

Family

ID=22938289

Family Applications (1)

Application Number Title Priority Date Filing Date
GB8209011A Expired GB2095557B (en) 1981-03-27 1982-03-26 Pest repellant

Country Status (7)

Country Link
JP (1) JPS5810507A (en)
BR (1) BR8201719A (en)
CA (1) CA1181684A (en)
GB (1) GB2095557B (en)
IL (1) IL65349A0 (en)
PL (1) PL235833A1 (en)
ZA (1) ZA822013B (en)

Also Published As

Publication number Publication date
IL65349A0 (en) 1982-05-31
JPS5810507A (en) 1983-01-21
BR8201719A (en) 1983-02-22
ZA822013B (en) 1983-02-23
PL235833A1 (en) 1982-12-20
GB2095557B (en) 1985-08-07
CA1181684A (en) 1985-01-29

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732 Registration of transactions, instruments or events in the register (sect. 32/1977)
732 Registration of transactions, instruments or events in the register (sect. 32/1977)
732 Registration of transactions, instruments or events in the register (sect. 32/1977)
PCNP Patent ceased through non-payment of renewal fee