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Publication #PI-83

IRAC's Insecticide Mode of Action Classification1

Frederick M. Fishel2

This guide explains the rationale behind the Insecticide Resistance Action Committee's (IRAC) insecticide and acaricide mode of action classification and provides a listing of those insecticide common names with their groupings, and primary modes of action for insecticides currently registered in Florida.

What is IRAC?

IRAC has groups formed in several countries, including the United States, Brazil, South Africa, Spain, India, and Australia. The group's purpose is to communicate and educate agricultural producers and crop protection professionals by providing resistance management information. Members of an IRAC group are generally professionals who are actively engaged in the insecticide and acaricide manufacturing industry. Some university researchers also participate.

Resistance to Pesticides

Resistance refers to an inheritable change in the sensitivity of a pest population that is reflected in the repeated failure of a product to achieve the expected level of control when used according to the label recommendation for that pest species. Resistance does not always occur, but has been documented with insecticides as early as 1914, and there are many known instances today where resistance is a problem. Not only has resistance occurred with insecticides, but other pesticides, such as fungicides, herbicides, and rodenticides. Complicating the understanding and management of resistance is the problem of knowing which type of resistance is present in a given pest population. For example, some pest populations are known to have cross-resistance. That is, they are not effectively controlled with pesticides having the same mode of action which generally target the same site within the pest. For example, both the carbamate and organophosphate insecticides target acetylcholine esterase, although each group of insecticides is chemically different from one another. The greatest resistance concern arises when multiple-resistance is confirmed. Multiple-resistance is the situation of a pest population that is resistant to pesticides having different modes of action. It is the most difficult type of resistance to manage, because the number of management options is reduced. For more information on resistance, see UF/IFAS EDIS Document ENY-624, 2005 Florida Citrus Pest Management Guide: Pesticide Resistance and Resistance Management.

IRAC's Classification Scheme

IRAC's insecticide classification scheme is based on mode of action. The goal of the scheme is to provide information to applicators of acaricides and insecticides so that they can make sound decisions on selecting insecticides to prevent or manage resistance. Besides selecting products that have different modes of action, growers are also encouraged to integrate other methods into insect and mite control programs. Table 1 contains those acaricides and insecticides registered for use in Florida, though it changes constantly. They are listed according to IRAC's classification scheme by their group and subgroup codes, primary target site of action, chemical sub-group or exemplifying active ingredient, and active ingredient, based on that appearing in The Pesticide Manual, 13th edition, 2003, edited by C.D.S. Tomlin, published by The British Crop Protection Council.

Using the IRAC Classification Scheme with Product Labels

IRAC is currently encouraging manufacturers of pesticides to indicate the IRAC mode of action group number and description on their product labels; some registrants are now doing so, especially with newer products. Such information would be helpful in assisting pesticide applicators in the selection of acaricides and insecticides for use in resistance management strategies. An example of the manner that IRAC is encouraging registrants to list this information:


Figure 1. 

Additional Information

  • IRAC: http://www.irac-online.org/groups/guide.

  • McCoy, C.W., M.E. Rogers, and L.W. Timmer. 2004. 2005 Florida citrus pest management guide: pesticide resistance and resistance management. UF/IFAS EDIS Document ENY-624. http://edis.ifas.ufl.edu/CG026.

  • Tomlin, C.D.S., ed. 2003. The pesticide manual: a world compendium, 13th edition. The British Crop Protection Council. 1250 pp., ISBN 1 901396 13 4.

Tables

Table 1. IRAC's classification scheme for acaricides and insecticides registered for use in Florida.

Group


Subgroup


Primary target site of action


Chemical subgroup or exemplifying active ingredient


Active ingredients


1*


1A


Acetylcholine esterase inhibitors


Carbamates


Aldicarb


Bendiocarb


Carbaryl


Carbofuran


Methiocarb


Methomyl


Oxamyl


Propoxur


Thiodicarb


1B


Organophosphates


Acephate


Azinphos-methyl


Chlorpyrifos


Chlorpyrifos-methyl


Coumaphos


Diazinon


Dichlorvos


Dicrotophos


Dimethoate


Disulfoton


Ethoprop


Fenamiphos


Fenthion


Isofenphos


Malathion


Methamidophos


Methidathion


Methyl parathion


Naled


Oxydemeton-methyl


Phorate


Profenofos


Propetamphos


Temephos


Terbufos


Tetrachlorvinphos


Trichlorfon


2*


2A


GABA-gated chloride channel antagonists


Cyclodiene organochlorines


Endosulfan


Lindane


2B


Fipronil (phenylpyrazoles)


Fipronil


3



Sodium channel modulators


Pyrethroids


Allethrin


d-cis-trans Allethrin


d-trans Allethrin


Bifenthrin


Bioallethrin S-cyclopentenyl


Cyfluthrin


Beta-Cyfluthrin


Cypermethrin


zeta-Cypermethrin


Cyphenothrin [(1R)-trans-isomers]


Deltamethrin


Esfenvalerate


Fenpropathrin


Fenvalerate


Imiprothrin


Permethrin


Phenothrin [(1R)-trans-isomer]


Prallethrin


Resmethrin


Tefluthrin


Tetramethrin


Tralomethrin


Pyrethrins


Pyrethrins (pyrethrum)


Methoxychlor


Methoxychlor


4*


4A


Nicotinic acetylcholine receptor agonists/antagonists


Neonicotinoids


Acetamiprid


Imidacloprid


Thiamethoxam


4B


Nicotine


Nicotine


6



Chloride channel activators


Avermectins, Milbemycins


Abamectin


7*


7A


Juvenile hormone mimics


Juvenile hormone analogues


Hydroprene


Kinoprene


Methoprene


7B


Fenoxycarb


Fenoxycarb


8*


8A


Compounds of unknown or non-specific mode of action (fumigants)


Methyl bromide


Methyl bromide and other alkyl halides


8B


Chloropicrin


Chloropicrin


8C


Sulfuryl fluoride


Sulfuryl fluoride


9*


9A


Compounds of unknown or non-specific mode of action (selective feeding blockers)


Cryolite


Cryolite


10*


10A


Compounds of unknown or non-specific mode of action (mite growth inhibitors)


Clofentezine


Clofentezine


Hexythiazox


Hexythiazox


10B


Etoxazole


Etoxazole


11*


11A1


Microbial disruptors of insect midgut membranes (includes transgenic crops expressing B.t. toxins)


B.t. var. israelensis


B.t. var. israelinsis


11B1


B.t. var. aizawai


B.t. var. aizawai


11B2


B.t. var. kurstaki


B.t. var. kurstaki


12*


12B


Inhibitors of oxidative phosphorylation, disruptors of ATP formation (inhibitors of ATP synthase)


Organotin miticides


Fentutatin oxide


12C


Propargite


Propargite


15



Inhibitors of chitin biosynthesis, type 0, Leptdopteran


Benzoylureas


Diflubenzuron


Hexaflumuron


Novaluron


17



Moulting disruptor, Dipteran


Cyromazine


Cyromazine


18*


18A


Ecdysone agonists/moulting disruptors


Diacylhydrazines


Halofenozide


Methoxyfenozide


Tebufenozide


18B


Azadirachtin


Azadirachtin


19



Octopaminergic agonists


Amitraz


Amitraz


20*


20A


Mitochondrial complex III electron transport inhibitors (Coupling site II)


Hydramethylnon


Hydramethylnon


21



Mitochondrial complex I electron transport inhibitors


METI acaricides, Rotenone


Rotenone


22



Voltage-dependent sodium channel blockers


Indoxacarb


Indoxacarb


24*


24A


Mitochondrial complex IV electron transport inhibitors


Aluminum phosphide


Aluminum phosphide


24C


Phosphine


Phosphine


25



Neuronal inhibitors (unknown mode of action)


Bifenazate


Bifenazate


27*


27A


Synergists


P450 monooxygenase inhibitors


Piperonyl butoxide


UN


UNC


Compounds with unknown mode of action**


Dicofol


Dicofol


UND


Pyridalyl


Pyridalyl


NS


NSA


Miscellaneous non-specific (multi-site) inhibitors


Borax


Borax


*Groups and Sub-groups: although sharing the same primary target site, it is possible that not all members of a single mode of action class have been shown to be cross-resistant. Different resistance mechanisms that are not linked to the target site, such as enhanced metabolism, may be common for such a group of chemicals. In such cases, the mode of action grouping is further divided into sub-groups.

**A compound with an unknown mode of action or an unknown mode of toxicity will be held in category UN until evidence becomes available to enable that compound to be assigned to a more appropriate mode of action class.

Category NS is used for compounds or preparations with a non-specific, multisite action.






Footnotes

1. This document is PI-83, one of a series of the Pesticide Information Office, Florida Cooperative Extension Service, Institute of Food and Agricultural Sciences, University of Florida. Original publication date October 2005. Visit the EDIS Web Site at http://edis.ifas.ufl.edu.

2. Frederick M. Fishel, Associate Professor, Agronomy Department, and Director, Pesticide Information Office; Florida Cooperative Extension Service, Institute of Food and Agricultural Sciences, University of Florida, Gainesville, FL 32611.


The Institute of Food and Agricultural Sciences (IFAS) is an Equal Opportunity Institution authorized to provide research, educational information and other services only to individuals and institutions that function with non-discrimination with respect to race, creed, color, religion, age, disability, sex, sexual orientation, marital status, national origin, political opinions or affiliations. For more information on obtaining other extension publications, contact your county Cooperative Extension service.

U.S. Department of Agriculture, Cooperative Extension Service, University of Florida, IFAS, Florida A. & M. University Cooperative Extension Program, and Boards of County Commissioners Cooperating. Larry Arrington, Dean.